VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 11/12/2021
** VAERS DATABASE Last updated: November 12, 2021**
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Manufacturers

Total Manufacturer
199,106MODERNA
36,710JANSSEN
5,381PFIZER\BIONTECH
2,555GLAXOSMITHKLINE BIOLOGICALS
1,469UNKNOWN MANUFACTURER
897MERCK & CO. INC.
627SEQIRUS, INC.
112DYNAVAX TECHNOLOGIES CORPORATION
91SANOFI PASTEUR
75NOVARTIS VACCINES AND DIAGNOSTICS
40EMERGENT BIOSOLUTIONS
14PAXVAX
12TEVA PHARMACEUTICALS
12PROTEIN SCIENCES CORPORATION
9PFIZER\WYETH
4BERNA BIOTECH, LTD.
4SMITHKLINE BEECHAM
3INTERCELL AG
1MEDIMMUNE VACCINES, INC.
1CSL LIMITED

COVID19 Lot Number

VAX LOT Total
2S9CL7,949
7,473
2,547
1,506
1,187
1,051
1,049
s0294561,043
866
IMM209861
816
UT7065MA766
657
579
U62828AA563
557
538
U6737AA516
515
S034636506
4F472471
458
P100253275449
444
276563436
429
418
4BH32414
MENVEO404
PP9L5362
UJ446AA337
319
306
290
271
49TM3270
R1B252M253
4F472179
933622147
C5763AA144
CW3116134
3Y7NL126
UNK114
113
ARBA141A105
104
103
96
300057A90
79
1F4EB73
R1B743M62
56
UJ090AA55
51
UH894AB46
45
UNK44
UNK42
42
EJ168638
Unknown36
35
34
32
32
26
el128424
24
A115A22
22
EN620222
21
UNK20
20
19
Z127A19
19
17
JEV18K95E15
12
111798PI12
10
A739088
No batch number8
3333324181078
6
6
TAR356
5
5
U6935AA5
UNK5
4
unknown4
3
2
55RB72
2
2
2
2
2
U7124AA2
JEV18A68E2
2
ABYB05BA1
1
1
1
1
AMVA436A1
1
1
TJ3521
A130A; VIS give1
1
U7140BB1
1
1
SP UP016AA1
1
1808P08802/ESV01
037K20A300,947
EL1284288,578
57,766
1,432

Incidents per State

State Total
82,750
CA62,821
FL38,209
TX36,512
NY34,921
PA23,646
IN23,622
IL20,597
MI19,590
OH19,426
NJ18,413
NC16,769
GA15,932
WA15,351
VA15,234
MA14,876
AZ14,206
MN12,940
MD12,656
CO11,908
WI11,425
MO10,240
TN9,685
OR8,768
KY8,437
CT8,300
SC6,700
OK6,293
AL5,692
LA5,025
IA4,825
KS4,821
UT4,637
NV4,374
NM3,967
AR3,807
ME3,161
NH3,096
NE2,918
MS2,859
ID2,785
WV2,469
HI2,459
PR2,417
MT2,414
RI2,076
DE1,868
AK1,830
VT1,734
DC1,715
ND1,388
SD1,269
WY866
GU118
VI69
AS47
MP29
MH8
XB6
FM4
QM3
XV2
XL1

ID: 1673680
Sex: M
Age: 32
State: NY

Vax Date: 09/03/2021
Onset Date: 09/03/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Seizure-Severe

Other Meds:

Current Illness:

ID: 1673681
Sex: F
Age: 72
State: CA

Vax Date: 09/01/2021
Onset Date: 09/03/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025L20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild

Other Meds:

Current Illness:

ID: 1673682
Sex: F
Age:
State: CA

Vax Date: 03/28/2021
Onset Date: 03/28/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EL1284
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chest discomfort, Dysphagia, Pain in extremity, Visual impairment

Symptoms: Injection site arm pain that lasted for 36 hours.; Joint pain and got worse in the next 24hours; As with first dose, skin allergic reactions that by now healed reappeared 1 day after the shot.; This is a spontaneous report from a contactable consumer, the patient. A 29-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8732), via an unspecified route of administration in the left arm on 28Mar2021 at 10:30 (at the age of 29-years-old) as dose 2, single for COVID-19 immunisation. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6199), via an unspecified route of administration in left arm on 07Mar2021 at 10:30 (at the age of 29-years-old) as dose 1, single for COVID-19 immunisation and experienced vaccination site pain and allergic skin reactions.Medical history included hashimotos thyroiditis and over active immune system. Concomitant medications included 50 mcg of levothyroxine (MANUFACTURER UNKNOWN) and 150mg of flucanazole (DIFLUCAN), both for an unknown indication, from unknown duration and unknown if ongoing. The patient was allergic to adhesive bandages, lemon grass and pea plant but not peas. The patient had not received any other vaccines within 4 weeks prior to the COVID vaccine. The patient had not been diagnosed with COVID-19 prior to the vaccination. The patient had not been tested for COVID-19 since the vaccination. On 28Mar2021, at 12:30, the patient had experienced vaccination site pain, which lasted for 36 hours and joint pain, which was felt few hours after the shot was given. Joint pain got worse in the next 24hours at which point pain medication was needed. The patient had also reported that as with first dose, skin allergic reactions that by then healed, reappeared one day after the shot. Therapeutic measures were taken as the result of adverse events, which included treatment with continued skin rash control for allergic skin rash and unknown point pain medication for joint pain. The events did not result in a visit to the doctors or other healthcare professional office/clinic visit, and emergency room/department or urgent care. The clinical outcome of the events vaccination site pain, joint pain were recovered in Unknown date in Mar2021 and allergic skin rash was not recovered at the time of report. No follow-up attempts are possible. No further information is expected.

Other Meds: LEVOTHYROXINE; DIFLUCAN

Current Illness:

ID: 1673683
Sex: F
Age:
State: IN

Vax Date: 03/26/2021
Onset Date: 03/01/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: unknown
Dose Series: UNK
Vax Route:
Vax Site:

Lab Data: Test Date: 20210329; Test Name: Bloodwork; Result Unstructured Data: Test Result:Elevated; Comments: high levels of something; Test Date: 202103; Test Name: Body temperature; Result Unstructured Data: Test Result:100.3 to 100.9 degrees; Comments: degrees; Test Date: 2021; Test Name: antibody test; Result Unstructured Data: Test Result:still has antibodies; Test Date: 20210330; Test Name: Ultrasound arm; Result Unstructured Data: Test Result:Did not show any blocked veins

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: Bruising and swelling underneath arm- purple bruising from under arm to wrist; Bruising and swelling underneath arm- purple bruising from under arm to wrist/ fingers were swelling; there was a spot on her arm that was raised a little and hard to touch, it felt like a knot.; tingling in her fingers; No appetite; Fever from 100.3 degrees to 100.9 degrees /she had a low grade fever; Terrible headache; lymph nodes swelling; Chills; Injection site was a little sore; very tired; Screaming diarrhea- very bad case of diarrhea; Throbbing in lymph nodes under arm, pain generated,tingling and feel tight like her arm and fingers were swelling was reported as worsened.; pain generated from her lymph nodes to her elbow and then as the day went on all the way down to her wrist; she started getting sick; just felt terrible all weekend and felt very lightheaded; two dime sized spots from her elbow to her wrist that are dark purple and very tender and swollen in that area; Body and joints ached; Body and joints ached; her arm was extremely sore; This is a spontaneous report from a contactable consumer (patient). A 54-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/Lot Number: ER8732; Expiration Date: 30Jun2021; NDC number: unknown) via an unspecified route of administration on 26Mar2021 at 08:40 (at the age of 54-years-old) in right arm as a single dose for covid-19 immunization. Medical history (including any illness at time of vaccination) included seasonal allergies, ongoing high blood pressure (diagnosed about 8-10 years ago), borderline diabetes from 2020 and ongoing, started on metformin last year and when checking her bloodwork for antibodies, the doctor noticed her sugar levels were high and started her on metformin, ongoing gout (first case of gout probably 10-12 years ago), covid very bad last year on 15Mar2020, it took about six weeks for her to recover, her doctor treated her at home. History of all previous immunization with the Pfizer vaccine considered as suspect, additional vaccines administered on same date of the Pfizer suspect, prior vaccinations (within 4 weeks), adverse events following prior vaccinations, family medical history relevant to adverse events were reported as none. This report is not report related to a study or programme. Concomitant medications included propranolol (PROPRANOLOL) taken for blood pressure abnormal from an unspecified start date and ongoing; metformin (METFORMIN) taken for glucose tolerance impaired from Dec2020 and ongoing; allopurinol (ALLOPURINOL) taken for gout from an unspecified start date and ongoing; diphenhydramine (DIPHENHYDRAMINE) taken for seasonal allergy from an unspecified start date and ongoing. The patient received the vaccine, and the injection site was a little sore and she started getting sick within 4 hours of being administered the Pfizer covid vaccine. Caller reported that on 26Mar2021, about two hours after the vaccine, she started feeling throbbing in her lymph nodes under her arm, the pain generated from her lymph nodes to her elbow and then as the day went on all the way down to her wrist. She was sicker than a dog all weekend, she had chills, fever of 100.3 degrees to 100.9 degrees, no appetite, terrible headache, she was very tired, she just felt terrible all weekend and felt very lightheaded. She was sick on 27Mar2021 and 28Mar2021. She kept noticing that her arm was extremely sore and by 28Mar2021, it was bruising underneath. Caller stated that there was purple bruising from her under arm to her wrist and tingling in her fingers. There was a spot on her arm that was raised a little and hard to touch, felt like a knot. She took pictures and the doctor said she needed to go to the emergency room because it looks like she may have a blood clot. She went to the emergency room, they looked at it and initially thought the same thing. They gave her a shot in the stomach of the blood thinner, but she forgets the name of the blood thinner. Caller stated that they did the ultrasound on 30Mar2021 and her doctor requested they call her from the room while she was in there. She explained that they didn't find anything in the veins, but her arm was still swollen and bruised, her hand, her fingers are tingly and tight. She was told to go home and put warm compresses or heat pads on it. They said it looks vascular, but they're not sure because the vaccine was new, they've never seen anybody react or reaction like this. The injection site was in the shoulder part where they normally put the needle. The problem was underneath where the lymph nodes are. Caller mentioned that she had the vaccine at 08:40, and she started to feel the throbbing in her lymph nodes around 11:00 am. Her chills started in the evening, probably around 18:30-19:00. She doesn't have the chills anymore, she had a low-grade fever with the chills until late Sunday night around 10:00 pm. Her fever was at 100.6 degrees or 100.9 degrees to 100.3 degrees, it would go back and forth. Soreness/lymph nodes swelling around 11 am, fever, headache started at 22:00 pm, diarrhea and chills started around 18:30-19:00, bruising was noticed on Sunday, exact time unknown, no appetite and tired started at 22:00. She was not admitted to the hospital, she just went to the emergency room on Monday evening, 29mar2021. She also had diarrhea, described as screaming diarrhea where you're up and down a lot. She doesn't know how else to describe it, in the country they call it screaming diarrhea and a very bad case of diarrhea, it started in the evening. She was very tired, and her body and joints ached as well. She reported her appetite was not back to where it normally is, but she was eating. She wasn't eating before; she was just drinking liquids over the weekend and didn't eat because she had a fever and diarrhea really bad. she doesn't feel like she had tons of energy, but she doesn't feel like she did over the weekend. Caller stated that she had it yesterday, but she had not noticed feeling lightheaded. Everything else went away, besides the pain in the lymph nodes in the arm. She just doesn't feel 100% yet as she was just dealing with her arm. The darker bruising was under her arm from her lymph nodes to her elbow and the lighter bruising was from her elbow to wrist. The yellow bruising was mixed in with the darker purple from her lymph nodes to elbow. There were two dime sized spots from her elbow to her wrist that are dark purple and very tender and swollen in that area. There was a lump that was raised last night that was on the other side where you bend your elbow. Caller explained that on the other side where the lump was yellow and light purple, and it was very sore. Caller stated that it could see on Sunday, but she could tell something wasn't right by 11:00 am on Friday because her arm felt very sore then and the soreness started going down her arm. She could tell that something was wrong. It felt tingly and tight like it was starting to swell but couldn't see any of the purple bruising until Sunday. It started with the bad lump and her arm was really hurting. Caller stated that her arm was the same, it was not getting worse or better. Caller mentioned that if it got worse, she doesn't know what else she can do. The doctors don't even know about the vaccine and they don't know what else to do. Caller reported that she is definitely not taking the second vaccine. She had the paperwork from when she went to the emergency room and had an ultrasound: results showed she did not have any blocked veins. Caller stated that on the paperwork, it has the receipt for her copy and the paperwork to show she got the shot for the blood thinner in stomach. She stated that she was looking at her paperwork and the diagnosis from emergency room visit was oedema of right upper extremity. Caller reported because she had covid last year, she gets tests done every month to check for antibodies and she still has antibodies. She was tested for antibodies two weeks ago and verified she still has antibodies. The patient underwent lab tests and procedures which included blood t

Other Meds: PROPRANOLOL; METFORMIN; ALLOPURINOL; DIPHENHYDRAMINE

Current Illness: Blood pressure abnormal (Diagnosed about 8-10 years ago); Borderline diabetes; Gout (First case of Gout probably 10-12 years ago)

ID: 1673684
Sex: F
Age:
State: MI

Vax Date: 01/25/2021
Onset Date: 01/01/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 20210202; Test Name: BP; Result Unstructured Data: Test Result: BP variation; Test Date: 20210208; Test Name: Blood test; Test Result: Negative; Test Date: 20210202; Test Name: Head CT scan; Result Unstructured Data: Test Result: Negative; Comments: negative, no clear etiology found in ED; Test Date: 20210209; Test Name: CRP; Result Unstructured Data: Test Result:18.725 (high); Test Date: 20210214; Test Name: CRP; Result Unstructured Data: Test Result:110.258-High; Test Date: 20210214; Test Name: Sed rate; Result Unstructured Data: Test Result:30-High; Test Date: 20210208; Test Name: COVID-19 antibody test; Test Result: Negative; Test Date: 20210208; Test Name: Nasal Swab; Test Result: Negative.

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: skin changes; hair loss; Nausea; did not sleep well due to achyness and muscle spasms; Legs seemed to get weak, wobbly and achy; intermittent headache; was awake during the night with increased leg pain and achyness; severe body aches; joint pain; Legs very painful- cant stand anything touching legs; brain fog; legs heavy; bilateral leg muscle spasms; 2 falls; Dizziness; metallic taste in mouth; when walking legs had visible shaking; Injury; hypotension; BP variation; HTN; standing and walking for more than a short distance caused extreme fatigue, weakness and some dizziness; standing and walking for more than a short distance caused extreme fatigue; standing and walking for more than a short distance caused extreme fatigue, weakness and some dizziness; bilateral tinnitus; anxiety; stress; hearing distortion; difficulty going from one computer monitor to the other/ difficulty walking; Difficulty standing- mild; mid vertigo; neurogenic pain of lower extremity, left; osteopenia; insomnia due to medical condition; essential hypertension, benign; The initial case was missing the following minimum criteria: unspecified AE. Upon receipt of follow-up information on 23Aug2021, this case now contains all required information to be considered valid. This is a spontaneous report from a contactable other HCP (health care profession) reported for herself via physician. A 58-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; Batch/Lot Number: EL9261), via intramuscular route, administered in left deltoid on 25Jan2021 (at the age of 58-year-old) as DOSE 1, SINGLE for COVID-19 immunization. Medical history included hypotension, Anxiety and depression from 18Oct2016, Arthropathy unspecified in knees and hands, asthma from 30Nov2011, Cardiac dysrhythmias, chronic sinusitis, complication of anesthesia, dysautonomia, GERD (gastrooesophageal reflux disease), hypothyroidism, menopause from 15Oct2012, migraines, morbid obesity with BMI (body mass index) of 40.0 44.9, adult from 19Oct2016, motion sickness, osteopenia, cardiovascular disease, pneumonia, unspecified visual loss, alcohol use, heart disease unspecified, orthostatic hypotension, headache, exercise intolerance, heart palpitation, hyperlipidemia, irregular heartbeat, AFib, OSA (obstructive sleep apnea), tends to be tachycardiac, hole in heart, post-menopausal syndrome, allergies to adhesive tape, allergy to suture; red dye; penicillin; sulfonamide, alcohol use, non smoker and COVID-19. The patient's concomitant medications were not reported. The patient previously took metoclopramide, azithromycin, cetirizine, iodine Budesonide metoprolol succinate (TOPROL) and solifenacin succinate (VESICARE) and experienced allergy for all of them. The patient had the family history as such: her mother was having cataract, macular degeneration, cancer of colon, pancreas and liver, her father had cataract, glaucoma, heart disease, heart bypass, atrial fibrillation, had pacemaker, diabetes and other Wolfe Parkinson white while her brother had lung cancer and orthostatic hypotension. On 28Jan2021, the patient had difficulty standing- mild and had difficulty while going from one computer monitor to the other. In Jan2021, the patient had mild vertigo. On 30Jan2021, hearing distortion and by 01Feb2021 standing and walking for more than a short distance caused extreme fatigue, weakness and some dizziness. very hard work. On 02Feb21 BP (blood pressure) variations, HTN (hypertension) and hypotension- send to ED (Emergency department) from work head CT (Computerized tomogram) done and it was negative, no clear etiology found in ED. On 03Feb2021 symptoms evolved, had 2 falls when walking legs had visible shaking. Started using a walker. Symptoms at this point: difficulty walking, legs heavy, hearing distortion, metallic taste in mouth, bilateral leg muscle spasms, dizziness, brain fog, very fatigue and weak 04Feb2021-same symptoms as 03Feb2021 but leg shaking was more pronounced and CRP (C-reactive protein) was 18.725. On 05Feb2021, additional symptoms were the patient woke up in the night with severe body aches and joint pain. No fever no cough. Legs were very painful- couldn't stand. Seemed weaker overall. COVID test and antibody test recommended and both came back negative on the same day of 05Feb2021. 07Feb2021-leg shakiness only if up walking, rest of symptoms from 06Feb2021 were the same. Leg/foot pumps were added. On 08Feb2021-body aches and leg pain got some better. No change in other symptoms. Patient had long talk with doctor and the doctor felt that symptoms were due to COVID vaccine. On 09Feb2021-no changes seen in symptoms, doctor added vitamin D3 10,000 IU, zinc 50 mg twice daily, vitamin C 1000 mg twice daily and Quercitin 500 mg twice daily and Lipo- Flavonnid plus ear health 2 tabs twice daily. On 10Feb2021-same symptoms occurred but tried adding legs lifts to foot pumps and hourly walks around the house assisted by walker which made legs ached more. Legs felt weaker but the patient did them anyway. On 11Feb2021, patient was awake during the night with increased leg pain and achiness. It was reported that the patient will try leg lifts every other hour instead of hourly. Symptoms were as of 11Feb2021: hearing distortion, intermittent headache, intermittent muscle spasms of the legs and arms, intermittent weakness and leg pain, brain fog, metallic taste in mouth, general feeling of weakness and fatigue. Tried to do leg lifts but legs too painful. On 12Feb2021-did leg lifts 3 times today, it was better day today. Patient informed she will try shower tomorrow with a shower chair. On 13Feb2021 the patient did shower today, had leg shaking mostly in left leg but overwhelming feeling of fatigue and weakness. But the patient still did the leg lifts x3. Left leg much harder to do than right. Had increased muscle spasms and cramping. On 14Feb2021-seemed to have increased hearing distortion and craft had to stop due to weakness and needed a nap. Overall, the patient was not feeling well. 15Feb2021, the patient tried to do things but seemed to "hit" a wall after a short time. Legs seemed to get weak, wobbly and achy. The patient was still doing leg lifts 3 times a day with foot pumps. Left leg was still worse. Metallic taste in mouth got better, ears no change, the patient tried a little walking without the walker and still it was not safe as the patient reported. On 16Feb202, the patient did not sleep well due to achiness and muscle spasms. Headache got back today and legs were heavy/wobbly on 16Mar2021. On 10Mar2021, Physical therapy ordered. On 11Mar2021, physical therapy started once weekly through 02Apr2021, minimal improvement. On 24Mar2021-went back to work remotely as unable to walk without walker still. On 03April2021, the symptoms were brain fog which made it extremely difficult to work, an example was typing and cut a word the first letter is correct and the rest was jumbled. Hearing distortion-sometimes volume got loud, intermittent beeping in hearing which made her sometimes had vertigo and nausea, legs were shaky but after being up for a longer amount of time. Half day at work was very difficult due to hitting a wall had extreme fatigue and brain fog got worse as the day goes on. Additional symptoms were hair loss and skin changed. As on 06May2021, the patient was taking olmesartan (BENICAR) 20 mg tablet, potassium chloride 20 mEq tablet, sucralfate (CARAFATE) 1 g tablet, valacyclovir (VALTREX) 500 mg tablet, vitamin coral, vitamin D2 oral, zinc oral. It was considered that the patient was having fatigue, unspecified type, brain fog, neurogenic pain of lower extremity, essential hypertension, benign, osteopenia, unspecified location, hair loss. The treatment with paracetamol (TYLENOL), alendronate-cholecalciferol (FOSAMAX PLUS D) 70 mg-2,800 unit per tablet and spironolactone (ALDACTONE) 50 mg tablet were started. The patient was put on a trail of Aldactone for hair loss and the pain medication was refilled and the patient was called for follow up after 3 months. It was reported that the patient understood and agreed of the treatment plan and will follow as directed.

Other Meds:

Current Illness:

ID: 1673685
Sex: F
Age:
State: OH

Vax Date: 03/12/2021
Onset Date: 03/12/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: FLUC4
Manufacturer: SEQIRUS, INC.
Vax Name: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT)
Lot: 276563
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data: Test Name: weight; Result Unstructured Data: Test Result:200 lbs; Comments: Weight: Unknown, patient says she weighs about 200lbs.

Allergies:

Symptom List: Chills, Confusional state, Eye inflammation, Headache, Laboratory test

Symptoms: they feel it could be an allergic reaction; big bump; her elbow was really sore; she was very tired; swelling; large welt; injection site hurt/She says the welt underneath was hard, raised, firm to the touch, and sore to the touch; Injection site redness; This is a spontaneous report from a two contactable consumer. This consumer (mother) and 34-year-old female consumer (patient) reported that she received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EN6206) via an unspecified route of administration on 12Mar2021 at 14:00 hours in left arm (at 34-year-old), as dose 1, single for COVID-19 immunization. The patient's medical history was reported as none and no concomitant medications and investigation assessment were received. On 12Mar2021, the patient experienced injection site hurt/she says the welt underneath was hard, raised, firm to the touch, and sore to the touch, injection site redness. Patient said that her reaction began the next morning or overnight. She said it hurted right away, and was achy which was a common thing. She woke up with a big bump about the size of a half dollar, with the redness being twice the size of the bump. Her area of redness was more oblong than round, her mom's was round. Patient took Ibuprofen before bed because she was aching a little. Ibuprofen. Patient took one pill of the regular strength, dosage unknown. The redness grew and got bigger and welt got bigger. The welt was not as big as the red area. The analogy they have been using was the red area was around the size of a hamburger bun, just the redness. The welt underneath was hard, raised, firm to the touch, and sore to the touch. Consumer had a few other side effects. This only happened to her, and it went away after 4 days or so, but day 10 the bump came back and it was not quite as big a bump, but it hurted with a red lump underneath it, and when she moved her arm it was achy. She felt like was it was also in her neck a little bit and the back of neck and shoulder were sore. Her arm was still a little achy after 3 weeks. She clarified that the injection site for both of them was where all lumps and redness were. Her injection site was itchy, but this was not true for her daughter. Consumer's daughter said that her elbow was really sore for 5-6 days, and she was very tired, which was a common side effect. She says she slept for hours and hours. Caller's daughter said that the main thing that was out of the norm was the red bump, swelling or welt, and redness. Her reaction lasted longer, the redness and lump, they lasted 5-6 days, and hers went away. Consumer says she would like to know if they should get the second shot, since they were turned away and told to call the number. She says she thinks that was to make sure that they wouldn't have a more severe reaction with the second dose, they were told to see what Pfizer thinks. Caller also experienced arm soreness, neck tightness, itching and achy. Caller wanted to know the time frame for the second dose, would it be less effective if taken later then 21 days. It was mentioned that consumer and her daughter had an allergic reaction to the first dose of Pfizer vaccine. When they went to get the second shot, they were turned away because the HCP was worried it may be worse than the first allergic reaction and referred the caller to call Pfizer. The event outcome was unknown. No follow-up attempts were possible. No further information was expected.

Other Meds:

Current Illness:

ID: 1673686
Sex: F
Age:
State: GA

Vax Date: 04/05/2021
Onset Date: 04/06/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: This is a spontaneous report from a contactable consumer. A 40-year-old non-pregnant female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EP6955) via an unspecified route of administration (age at vaccination 40 years) on 05Apr2021 as a single dose in arm for COVID-19 immunisation. Medical history and Concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, it was unknown whether the patient had been tested for COVID-19. It was unknown whether the patient received any other vaccines within four weeks prior to the COVID vaccine. On 06Apr2021, the patient experienced a big ball of a lump under her armpit of the arm at the vaccination site. The events did not result in a visit to the doctors or other healthcare professional office/clinic visit, and emergency room/department or urgent care. No therapeutic measures were taken as a result of the reported event. The clinical outcome of big ball of a lump under armpit was unknown. No follow-up attempts are needed. No further information is expected. Amendment: This follow-up report is being submitted to amend previously reported information: Updated age at Vaccination and updated event code from "Lymphadenopathy " to "vaccination site mass"

Other Meds:

Current Illness:

ID: 1673687
Sex: F
Age:
State: CA

Vax Date: 04/01/2021
Onset Date: 04/02/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 20210402; Test Name: Fever; Result Unstructured Data: Test Result:104.5

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: Fever of 104.5; Chills; Nausea; Joint pain; She really is very miserable; She is ill; This is a spontaneous report from a contactable consumer or other non hcp. A 60-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: unknown), via an unspecified route of administration on 01Apr2021 (at the age of 60-years-old) as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunisation. Medical history was none. The patient's concomitant medications were not reported. The patient experienced fever of 104.5, chills, nausea, joint pain, she really is very miserable, she is ill on 02Apr2021 and I don't know what to do. Reporter stated, "I really do not know, I am just reading from the paper that she was given at the time of the vaccine. So I do not know the LOT#. I do not have her vaccination card . The patient underwent lab tests and procedures which included body temperature: 104.5 on 02Apr2021. The outcome of all event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1673688
Sex: F
Age:
State: CO

Vax Date: 04/10/2021
Onset Date: 04/11/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: Vaginal bleeding; This is a spontaneous report from a contactable consumer or other non hcp(patient). A 30-years-old female patient received first dose of bnt162b2 (Pfizer covid 19 vaccine, formulation: solution for injection, Batch/Lot Number: EW0151), via an unspecified route of administration, administered in Arm Left on 10Apr2021 16:45 (at the age of 30-years-old) as single dose for COVID-19 immunisation. Medical history included endometriosis from an unknown date and unknown if ongoing Other medical history: Endometriosis. The patient had no allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Concomitant medications included diphtheria vaccine toxoid, pertussis vaccine acellular, tetanus vaccine toxoid (TDAP) taken for an unspecified indication from 12Mar2021 to 12Mar2021; cyanocobalamin (VITAMIN B12) taken for an unspecified indication, start and stop date were not reported; colecalciferol (VITAMIN D 3) taken for an unspecified indication, start and stop date were not reported. On 11Apr2021 14:30, the patient experienced vaginal bleeding. The outcome of the event was not recovered. Follow-up attempts completed. No further information expected.

Other Meds: VITAMIN B12 [CYANOCOBALAMIN]; VITAMIN D 3

Current Illness:

ID: 1673689
Sex: M
Age:
State: NC

Vax Date: 04/05/2021
Onset Date: 04/06/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J201A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 20210406; Test Name: blood pressure; Result Unstructured Data: Test Result:120/80s; Comments: Nitroglycerin brought pressure to 120/80s but it went back up to 140 afterward.; Test Date: 20210406; Test Name: Blood pressure; Result Unstructured Data: Test Result:140s/90s; Comments: High; Test Date: 20210406; Test Name: Blood Pressure; Result Unstructured Data: Test Result:spiked up to almost the high/90s; Test Date: 20210406; Test Name: EKGs; Result Unstructured Data: Test Result:Normal; Test Date: 20210407; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20210406; Test Name: Troponin tests; Result Unstructured Data: Test Result:Normal; Test Date: 20210406; Test Name: X-ray; Result Unstructured Data: Test Result:normal

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: This is a spontaneous report from a contactable consumer or other non hcp (patient). A 53-year-old male patient received bnt162b2 (BNT162B2 PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot number: ER8733), via an unspecified route of administration in arm left on 05Apr2021 at 09:45 (at the age of 53-years-old) as dose 1, single for COVID-19 immunisation. The medical history of the patient included hypertension and asthma. The known allergies of the patient was reported as mild allergy to apples, carrots, nuts. The concomitant medications of the patient included clarithromycin (CLARITIN [CLARITHROMYCIN]), escitalopram (ESCITALOPRAM), omeprazole (PROTONIX [OMEPRAZOLE]), losartan (LOSARTAN) all taken for an unspecified indication, start and stop date were not reported. The patient previously took albuterol sulfate and experienced adverse reaction. The patient did not receive any other vaccines within 4 weeks prior to the covid vaccine. Prior to vaccination, the patient was not diagnosed with covid-19. Since the vaccination, the patient had been tested negative with covid-19. On 06Apr2021 at 20:00, the patient experienced 34 hours after my shot, i felt pressure and discomfort in my chest, tingling in my left arm and blood pressure was high. The patient stated the next morning he felt fine and had resumed normal activity. His cardiologist did and exam and said it was not an arterial issue and agreed it may have been a reaction to the vaccine. His blood pressure spiked up to almost the high/9Os. The events resulted in emergency room visit and physician office visit. The patient underwent lab tests and procedures which included Nitroglycerin brought pressure to 120/80s but it went back up to 140 afterward (blood pressure measurement): 120/80s on 06Apr2021, blood pressure measurement: 140s/90s on 06Apr2021, blood pressure measurement: spiked up to almost the high/90s on 06Apr2021, EKGs: normal on 06Apr2021, troponin tests: normal on 06Apr2021, x-ray: normal on 06Apr2021 and Nasal swab sars-cov-2 test: negative on 07Apr2021. Therapeutic measures were taken as a result of events that included patient took aprazolam, and a glass of red wine, it did not subside and nitroglycerin in hospital. The patient recovered from 34 hours after my shot, i felt pressure and discomfort in my chest, tingling in my left arm on an unspecified date in 2021 and the outcome of the event blood pressure was high 140s/90s was reported as unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: CLARITIN [CLARITHROMYCIN]; ESCITALOPRAM; PROTONIX [OMEPRAZOLE]; LOSARTAN

Current Illness:

ID: 1673690
Sex: M
Age:
State: CA

Vax Date: 03/19/2021
Onset Date: 03/26/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data: Test Date: 20210326; Test Name: Blood Pressure; Result Unstructured Data: Test Result:191/112; Test Date: 20210326; Test Name: heart rate; Result Unstructured Data: Test Result:178bpm

Allergies:

Symptom List: Vaccination site erythema, Vaccination site pruritus, Vaccination site swelling

Symptoms: my blood pressure shot up to 191/112; heart rate of 178 bpm; Vision got blurry; skin got clammy; This is a spontaneous report from a contactable consumer (patient). A 63-year-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: ew6206), via an unspecified route in the left arm on 19Mar2021 (age at vaccination: 63-year-old), as a single dose for covid-19 immunization. Medical history included high Blood pressure (BP), hemochromatosis, acid reflux, cholesterol and known allergies: codeine. The patient concomitant medications were not reported. Historical vaccine included first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: E19267), via an unspecified route in the left arm on 26Feb2021 at 15:45 (age at vaccination: 63-year-old), as a single dose for covid-19 immunization. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient received unknown medications within 2 weeks of vaccination. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient has not been tested for COVID-19. On 26Mar2021 at 12:00 am, eight hours after receiving second dose, patient blood pressure shot up to 191/112, with a heart rate of 178 bpm, vision got blurry, and skin got clammy. Patient did not receive any treatment for the events. The patient underwent lab test and procedure on 26Mar2021 which included blood pressure shot up to 191/112 and heart rate of 178 bpm. The clinical outcome of the events was recovered unknown date in 2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1673691
Sex: M
Age:
State: PA

Vax Date: 04/08/2021
Onset Date: 04/09/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039k20a
Dose Series: 1
Vax Route: SYR
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: Abdominal pain; diarrhea; anal bleeding; Difficulty urinating; loss of appetite; Chills; This is a spontaneous report from a contactable consumer. This 58-year-old male consumer reported that: A 58-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EP7533), dose 1 via an unspecified route of administration, administered in Arm Right on 08Apr2021 02:30 (at the age of 58-years-old) as a single dose for covid-19 immunization. Medical history included none. There were no concomitant medications. The patient did not have any allergies. The patient had no other vaccine within four weeks and no other medications received within 2 weeks of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 09Apr2021, the patient experienced abdominal pain and diarrhea, anal bleeding, difficulty urinating, loss of appetite, chills. The patient did not receive any treatment. Outcome of the event was recovering, at the time of this report. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1673692
Sex: F
Age:
State: GA

Vax Date: 04/13/2021
Onset Date: 04/13/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 20210413; Test Name: blood pressure; Result Unstructured Data: Test Result:unable to read blood pressure twice; Test Date: 20210413; Test Name: Heart Rate; Result Unstructured Data: Test Result:165+

Allergies:

Symptom List: Blood pressure decreased, Chest pain, Chills, Confusional state, Decreased appetite

Symptoms: Lightheaded; heart rate of 165+; unable to read blood pressure twice; sick to stomach; unable to read uncontrollable head shake side to side; numbness in cheeks; tingling in feet; This is a spontaneous report from a contactable consumer or other non hcp. A 43-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration, administered in Arm Left on 13Apr2021 12:00 as dose 1, single (Age at vaccination 43-year-old) for covid-19 immunisation. The patient was not pregnant at the time of vaccination. Medical history included none. Concomitant medication(s) included ibuprofen (IBUPROFEN);ascorbic acid, ergocalciferol, folic acid, nicotinamide, panthenol, retinol, riboflavin, thiamine hydrochloride(MULTIVITAMINS). Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. No known allergies. On 13Apr2021 12:00, the patient experienced lightheaded, heart rate of 165+, unable to read blood pressure twice, sick to stomach, unable to read uncontrollable head shake side to side, numbness in cheeks, tingling in feet. The patient underwent lab tests and procedures which included blood pressure measurement was unable to read blood pressure twice on 13Apr2021 and heart rate was 165+ on 13Apr2021. Therapeutic measures were taken as a result of events includes water. The outcome for all events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: IBUPROFEN; MULTIVITAMINS [ASCORBIC ACID;ERGOCALCIFEROL;FOLIC ACID;NICOTINAMIDE;PANTHENOL;RETINOL;RIBOFLAVIN;THI

Current Illness:

ID: 1673693
Sex: F
Age:
State: TX

Vax Date: 04/02/2021
Onset Date: 04/06/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20-2A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Dyspnoea, Fatigue, Feeling abnormal, Head discomfort, Headache

Symptoms: severe muscle aches; yeast infection; thrush; This is a spontaneous report from a non-contactable consumer or other non hcp (patient). A 59-years-old non pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EP6955), via an unspecified route of administration, administered in Arm Left on 02Apr2021 08:15 as dose 2, single for covid-19 immunisation. The patient medical history was not reported. Patient had no known allergies. Patient was not pregnant at the time of vaccination. Concomitant medications included estradiol (ESTROGEN) taken for an unspecified indication, start and stop date were not reported; progesterone taken for an unspecified indication, start and stop date were not reported; rizatriptan taken for an unspecified indication, start and stop date were not reported; nortriptyline taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Patient previously took BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EN6206), via an unspecified route of administration, administered in Arm Left on 12Mar2021 08:15AM (at the age of 59-year-old) as dose 1, single for covid-19 immunisation and experienced severe muscle aches on day 2 post shot. On 06Apr2021, the patient experienced severe muscle aches, yeast infection, thrush. Therapeutic measures were taken as a result of events included Fluconazole, Nystatin. The events resulted in doctor or other healthcare professional office/clinic visit. The outcome of the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: ESTROGEN; PROGESTERONE; RIZATRIPTAN; NORTRIPTYLINE

Current Illness:

ID: 1673694
Sex: F
Age:
State: KY

Vax Date: 04/12/2021
Onset Date: 04/13/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 20210413; Test Name: blood pressure; Result Unstructured Data: Test Result:kept raising; Test Name: EKG; Result Unstructured Data: Test Result:Unknown result; Test Name: labs; Result Unstructured Data: Test Result:Unknown result

Allergies:

Symptom List: Heart rate decreased, Heart rate increased, Hypertension, Injection site pain, Musculoskeletal chest pain

Symptoms: my blood pressure kept raising despite taking bp meds; Fatigue; Chills; Fever; body aches; This is a spontaneous report from a contactable consumer reporting for herself. A 45-years-old non-pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), via an unspecified route of administration, administered in Arm Right on 12Apr2021 16:45 (Batch/Lot Number: EWO158, expiration date not reported) as single dose (at age of 45-years old) for covid-19 immunization. The patient medical history included hypertension from an unknown date and unknown if ongoing. Concomitant medications included labetalol; paracetamol (TYLENOL); ibuprofen taken for an unspecified indication, start and stop date were not reported. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot/Batch# ER8730, expiration date not reported), via unknown route in Left arm on 22Mar2021 as single dose (at age of 45-years old) for covid-19 immunization. The patient was allergy to Hydrocodone, oxytocin and similar meds, bacterium. Patient did not receive other vaccine in four weeks. No covid prior vaccination and no covid tested post vaccination. The patient experienced blood pressure kept raising despite taking BP meds, fatigue, chills, fever, and body aches on 13Apr2021 at 16:00. The patient ended up in the Emergency room/department or urgent care because of it. The patient underwent lab tests and procedures which included blood pressure measurement kept raising on 13Apr2021, electrocardiogram and laboratory test: unknown result on unknown date. Therapeutic measures were taken as a result of all events. The outcome of the events was recovering at the time of report. No follow up attempts are possible. No further information is expected.

Other Meds: LABETALOL; TYLENOL; IBUPROFEN

Current Illness:

ID: 1673695
Sex: M
Age:
State: AZ

Vax Date: 04/13/2021
Onset Date: 04/16/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Nausea, Pain, Pain in extremity, Paraesthesia oral, Pyrexia

Symptoms: Blood coming out of right ear; This is a spontaneous report from a contactable consumer or other non hcp. A 60-years-old male patient received bnt162b2 (BNT162B2, Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration, in Arm Left on 13Apr2021 20:00(age at vaccination: 60 Years) as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunisation. Patient didn't receive other vaccines within 4 weeks prior to vaccination. Medical history included renal disorder from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. Patient had no allergies, patient didn't had covid prior to vaccination, patient was not tested with covid-19 to post vaccination. The patient experienced blood coming out of right ear on 16Apr2021 03:00. No therapeutic measures were taken for the event. The outcome of the event ear haemorrhage was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1673696
Sex: F
Age:
State: AZ

Vax Date: 04/08/2021
Onset Date:
Rec V Date: 09/04/2021
Hospital:

Vax Type: DTAPHEPBIP
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: DTAP + HEPB + IPV (PEDIARIX)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: SARS-CoV-2 antibody test, SARS-CoV-2 test negative

Symptoms: Severe body aches; low oxygen; fatigue; chills; nausea; vomiting; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 57-years-old non pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration, administered in Arm Right on 08Apr2021 12:15 (at the age of 57-year-old) as dose number unknown, single for covid-19 immunisation. Medical history included migraine from an unknown date and unknown if ongoing Other medical history: Migraines sleep apnea pancreatic cancer remission umbilical hernia fibromyalgia, sleep apnoea syndrome from an unknown date and unknown if ongoing, pancreatic carcinoma from an unknown date and unknown if ongoing, umbilical hernia from an unknown date and unknown if ongoing, fibromyalgia from an unknown date and unknown if ongoing, drug hypersensitivity from an unknown date and unknown if ongoing to Cymbalta, lyrica, savella, prednisone, morphine. concomitant medications were not specified. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Patient previously took unspecified Pfizer vaccine administered in right arm on 18Mar2021 for immunisation. On an unspecified date in 2021, the patient experienced severe body aches, low oxygen, fatigue, chills, nausea, vomiting. No treatment was taken as a result of events. The events resulted in doctor or other healthcare professional office/clinic visit. The outcome of the events were recovered with sequel. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1673697
Sex: F
Age:
State:

Vax Date: 04/12/2021
Onset Date: 04/13/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: HIBV
Manufacturer: MERCK & CO. INC.
Vax Name: HIB (PEDVAXHIB)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: chills; joint pain; a strong headache; I started spotting, which is unusual; headache that worsened with movement; This is a spontaneous report from a non-contactable consumer or other non hcp. A 35-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection), dose 2 via an unspecified route of administration on 12Apr2021 10:00 (Batch/Lot Number: Ep753304) as dose 2, single (age at vaccination 35-year-old) for covid-19 immunisation. Medical history included known allergies: Pollen from an unknown date. Concomitant medication(s) included ibuprofen (IBUPROFEN) taken for an unspecified indication, start and stop date were not reported. Historical vaccine information included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection) 1st dose on 19Mar2021 (age at vaccination 34-year-old), lot number Ep7534 for Covid-19 immunisation. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient was not pregnant at the time of vaccination. On13Apr2021 12:00, the patient experienced chills, joint pain, a strong headache, i started spotting, which is unusual, headache that worsened with movement. The day after the second dose patient had chills, joint pain, and a strong headache that worsened with movement. The second day after the shot patient started spotting, which was unusual. Her period had ended 5 days before the shot. The outcome for all events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: IBUPROFEN

Current Illness:

ID: 1673698
Sex: F
Age:
State: AZ

Vax Date: 04/11/2021
Onset Date: 04/15/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: PNC13
Manufacturer: PFIZER\WYETH
Vax Name: PNEUMO (PREVNAR13)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: Vaginal bleeding as of mental cycle is about to begin the last 24 hrs; This is a spontaneous report from a contactable Consumer (patient herself). A 38-years-old female non-pregnant patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration, administered in Arm Left on 11Apr2021 at 07:45 am (at the age of 38-years-old) as a DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. No known allergies were reported. No other vaccine was administered in four weeks. Other medications in two weeks were none. Patient did not have covid prior vaccination and was not tested for covid post vaccination. The patient reported that, vaginal bleeding as of mental cycle is about to begin the last 24 hrs on 15Apr2021. Treatment was received for the event (unspecified). Outcome of the event was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1673699
Sex: F
Age:
State: NY

Vax Date: 03/14/2021
Onset Date: 04/05/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: RV1
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: ROTAVIRUS (ROTARIX)
Lot:
Dose Series: 1
Vax Route: PO
Vax Site: MO

Lab Data: Test Name: bloodwork; Result Unstructured Data: Test Result:high blood sedimentation rate; Test Name: c reactive protein; Result Unstructured Data: Test Result:high; Test Name: Eye exam; Result Unstructured Data: Test Result:came back normal; Test Date: 20210413; Test Name: Nasal swab test; Test Result: Negative

Allergies:

Symptom List: Blood pressure increased, Chest discomfort, Heart rate increased

Symptoms: severe flu like symptoms for 3 days starting 12 hours after shot; slight fever; chills; night sweats; body aches; severe chest pain; fatigue; persistent, throbbing pain in my right temple area; This is a spontaneous report from a contactable consumer(patient) reported that: A 32-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), dose 2 via an unspecified route of administration, administered in Arm Left on 14Mar2021 (Batch/Lot Number: EN6208) as DOSE 2, SINGLE for covid-19 immunization. The patient past Medical history included obesity from an unknown date and unknown if ongoing , hypothyroidism from an unknown date and unknown if ongoing , anxiety from an unknown date and unknown if ongoing , depression from an unknown date and unknown if ongoing , asthma from an unknown date and unknown if ongoing , sleep apnea syndrome from an unknown date and unknown if ongoing , headache from an unknown date and unknown if ongoing and hypersensitivity from an unknown date and unknown if ongoing. Concomitant medication(s) included levothyroxine sodium (SYNTHROID) taken for an unspecified indication, cetirizine (CETIRIZINE) taken for an unspecified indication, sertraline (SERTRALINE) taken for an unspecified indication, ethinylestradiol, ferrous fumarate and norethisterone acetate (AUROVELA FE 1.5/30) taken for an unspecified indication. The patient previously took vicodin and experienced drug hypersensitivity, bnt162b2 for covid-19 immunization. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccine within 4 weeks prior to covid-19 vaccination. After 2nd shot, the patient experienced severe flu like symptoms for 3 days starting 12 hours after shot. These include slight fever, chills, night sweats, body aches, severe chest pain and fatigue on 05Apr2021. Symptoms abated after day 3. At about 2 1/2 weeks later she donated blood. Three days later she developed persistent, throbbing pain in her right temple area. This continued for days, not helped by migraine medication, todarol nsaid shot, acetaminophen. TMJ and migraines were ruled out by doctors. Eye exam came back normal. Primary care ordered bloodwork and started me on steroids. Bloodwork indicated high blood sedimentation rate and high C-reactive protein which, combined with persistent temporal pain (2 weeks so far) and sensitivity to touch in temple, are highly indicative of temporal arteritis. Sars-cov-2 test: Negative on 13Apr2021. This is very abnormal in someone my age (32). She is waiting on approval for an MRI (insurance denied 1st request) and possible temporal artery biopsy to confirm. The events result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. The event outcome was Not recovered.

Other Meds: SYNTHROID; CETIRIZINE; SERTRALINE; AUROVELA FE 1.5/30

Current Illness:

ID: 1673700
Sex: F
Age:
State: OR

Vax Date: 04/02/2021
Onset Date: 04/02/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: Eh9899
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 20210402; Test Name: BP; Result Unstructured Data: Test Result:elevated; Comments: Also had elevated BP (mostly systolic of +15 to +35) 10 of the past 12 days since receiving the shot.

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Lymph node pain, Lymphadenopathy

Symptoms: Elevated BP (mostly systolic of +15 to +35) 10 of the past 12 days since receiving the shot; Day 1 & 2 fatigue. Got better by day 3. Gone by day 4. Reoccurred day 10 and gotten progressively worse; This is a spontaneous report from a contactable consumer. This 62-years-old non pregnant female consumer received bnt162b2 (BNT162B2, Pfizer-BioNTech Covid-19 mRNA Vaccine, Solution for injection, Batch/Lot number ewd150), via an unspecified route of administration, administered in Arm Right on 02Apr2021 11:00 as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunisation. Medical history included hypertension. There were no concomitant medications. No other vaccine in four weeks. Other medications in two weeks yes. No covid prior vaccination. No covid tested post vaccination. No known allergies. On 02Apr2021 19:00 patient experienced elevated blood pressure (mostly systolic of +15 to +35) 10 of the past 12 days since receiving the shot, day 1 & 2 fatigue. got better by day 3. gone by day 4. reoccurred day 10 and gotten progressively worse. The patient underwent lab tests and procedures which included blood pressure measurement: elevated on 02Apr2021 Also had elevated BP (mostly systolic of +15 to +35) 10 of the past 12 days since receiving the shot. No treatment was received for AE. The outcome of both events was not recovered. No follow up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1673701
Sex: F
Age:
State: OH

Vax Date: 02/08/2021
Onset Date: 02/09/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Name: fever; Result Unstructured Data: Test Result:102.5; Test Name: CT scan; Result Unstructured Data: Test Result:Unknown results; Test Name: X-ray; Result Unstructured Data: Test Result:Unknown results

Allergies:

Symptom List: Unevaluable event

Symptoms: Shortness of breath; fever 102.5; extreme weakness pain all over; burning of hands and feet; elevated D-Dimer; pain all over; This is a spontaneous report from a contactable Nurse. This 46-year-old female Nurse (patient). A 46-year-old (non-pregnant) female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: unknown, Expiration date: unknown), via unspecified route, administered in left arm on 08Feb2021 (at the age of 46-year-old) as dose 1, single for COVID-19 immunization. Patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: unknown, Expiration date: unknown), via unspecified route, administered in left arm on 18Jan2021 (at the age of 46-year-old) as dose 1, single for COVID-19 immunization. The patient medical history includes Diabetes mellitus, Osteoporosis, Obesity, Hypovitaminosis, osteopenia, COVID-19, pneumonia, Irritable bowel syndrome, anxiety and depression all from an unspecified onset to unknown ongoing and concomitant medications were not reported. Past drug event includes Morphine induced Drug hypersensitivity, Bactrim induced Drug hypersensitivity and laytex induced Drug hypersensitivity. On 09Feb2021, after the vaccination, the patient experienced Shortness of breath, fever 102.5, extreme weakness, pain all over, burning of hands and feet elevated D-Dimer. Adverse event resulted in Emergency room/department or urgent care. Treatment was received with: IV Ativan, X-ray Labs and CT scan. The patient lab data includes body temperature with a reading of 102.5-degree Fahrenheit on an unspecified date. CT scan and X-RAY on an unspecified date with unknown results. Patient was found covid positive prior vaccination and patient was not tested for covid post vaccination. The outcome of the events was recovering at the time of this report. No follow-up attempts possible. No further information expected.

Other Meds:

Current Illness:

ID: 1673702
Sex: F
Age:
State: NJ

Vax Date: 02/03/2021
Onset Date: 02/03/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 20210203; Test Name: blood pressure; Result Unstructured Data: Test Result:Elevated SBP 190's; Test Date: 20210203; Test Name: blood pressure; Result Unstructured Data: Test Result:SBP gtearter than 200; Test Date: 20210223; Test Name: covid test; Test Result: Negative ; Comments: Nasal swab; Test Date: 20210223; Test Name: covid test; Test Result: Negative ; Comments: Interp Nasal Swab; Test Date: 20210308; Test Name: covid test; Test Result: Negative ; Comments: Nasal swab; Test Date: 20210308; Test Name: covid test; Test Result: Negative ; Comments: Interp Nasal Swab

Allergies:

Symptom List: Chills, Dizziness, Injection site pain, Myalgia, Pyrexia

Symptoms: headache; Lightheaded/dizzy; Elevated SBP 190's, monitored for additional 15min SBP greater than 200; This is a spontaneous report from a contactable Nurse reported for herself. A 61-year-old non-pregnant female patient received first dose of bnt162b2 (Pfizer covid-19 vaccine, Solution for injection, Lot number: EJ1686), via an unspecified route in the left arm on 03Feb2021 at 08:00 (age at vaccination: 61-year-old), as a single dose for covid-19 immunization. Medical history included breast CA, cerebrovascular accident (CVA), migraines, osteopenia, insomnia, hypertension (HTN)-new and known allergies with Levaquin, latex, metoclopramide, ondansetron, clarithromycin, statins, Zyvox and Ambien and penicillin (PCN). Concomitant medications included bupropion hydrochloride (WELLBUTRIN), cetirizine hydrochloride (ZYRTEC), alprazolam (XANAX), pitavastatin calcium (LIVALO), temazepam and Vitamin. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, patient was not diagnosed with COVID-19. On 03Feb2021 at 08:00 after 15 min, patient developed headache, upon standing became lightheaded and dizzy with Elevated SBP 190's, monitored for additional 15min SBP greater than 200. Patient was taken to Emergency Room. Since that time have had headaches, lightheadedness, dizziness and have had elevated BP since this time. Now diagnosed with high blood pressure - new diagnosis and on HTN medications. Adverse events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. Therapeutic measures taken as a result of the events included emergency room: IVF labs, F/U with primary care physician for further management. The patient underwent lab test and procedure which included blood pressure elevated SBP 190's and SBP greater than 200 on 03Feb2021; post vaccination antibodies test: SARS-CoV-2 Nasal Swab: Negative on 23Feb2021; SARS-CoV-2 Interp Nasal Swab: Negative on 23Feb2021; SARS-CoV-2 Nasal Swab: Negative on 08Mar2021 and SARS-CoV-2 Interp Nasal Swab: Negative on 08Mar2021. The clinical outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: WELLBUTRIN; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; XANAX; LIVALO; TEMAZEPAM

Current Illness:

ID: 1673703
Sex: F
Age:
State: UT

Vax Date: 04/16/2021
Onset Date: 04/16/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011L20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: Fatigue; Dry mouth; Slight fever; Clamminess; Pain in upper right arm; Joints became stiff; Itchy on right arm/hand; Headache; Dizziness; Nauseated; Could not sleep; Feeling tingling throughout right side; This is a spontaneous report from a contactable consumer, the patient. A 35-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0164) via an unspecified route of administration in the right arm on 16Apr2021 (at the age of 35-year-old) as a single dose for COVID-19 immunisation. Medical history included irritable bowel syndrome with diarrhea (IBS-D), high blood pressure, sciatica (Sciatic Nerve Lower Back Pain), scoliosis, laryngopharyngeal reflux (silent reflux), gastroesophageal reflux disease (GERD), gastroparesis and food allergy (gelatin). The patient previously took vibramycin, doxycycline, tetracycline and flagyl and experienced allergy to these medications. Prior to the vaccination, the patient was no diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included metoprolol succinate ER (MANUFACTURER UNKNOWN), pantoprazole sodium sesquihydrate (pantoprazole sodium) (MANUFACTURER UNKNOWN) and tramadol (MANUFACTURER UNKNOWN) all for unknown indication from an unknown date. On 16Apr2021, 15 minutes after the shot she felt fine. 30 minutes after the shot she started feeling tingling throughout her right side, along with pain in her upper right arm. 45 minutes after the shot her joints became stiff and she started becoming itchy on her right arm/hand. 60 minutes after the shot she started getting a headache and dizziness. 90 minutes after the shot she got nauseated. She could not sleep that night because of the dizziness. On 17Apr2021, next day all of the same symptoms plus fatigue, dry mouth and a slight fever with clamminess. Two days after the shot no more tingling, less pain in the arm, joints were a little looser, still had a headache, some dizziness, and still had a dry mouth. The patient did not receive any treatment for the events. The events did not result in doctor or other healthcare professional office or clinic visit, and emergency room or department or urgent care. The clinical outcome of the events feeling tingling throughout right side was resolved on 18Apr2021. The clinical outcome of the events joints became stiff, dizziness, could not sleep, pain in upper right arm was resolving and that of itchy on right arm/hand, headache, nauseated, fatigue, dry mouth, slight fever and clamminess was not resolved at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds: Metoprolol Succinate; Pantoprazole Sodium; Tramadol

Current Illness:

ID: 1673704
Sex: M
Age:
State: CA

Vax Date: 04/16/2021
Onset Date: 04/17/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: Severe lower backpain; This is a spontaneous report from a contactable consumer, the patient. A 37-year-old male patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 16Apr2021 at 10:00, as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. On 17Apr2021 at 23:45, the patient experienced severe lower backpain. The patient had no known history of back pain. The event did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the event. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event severe lower backpain was not resolved at the time of this report. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1673705
Sex: M
Age:
State: HI

Vax Date: 04/06/2021
Onset Date: 04/14/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Arthralgia, Chills, Headache, Mobility decreased, Myalgia

Symptoms: Hives on chest, left arm, and stomach; Some itchiness on the arm; This is a spontaneous report from a contactable consumer, the patient. A 59-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8734) via an unspecified route of administration in the left arm on 06Apr2021 at 16:00 (at the age of 59-years-old) as a single dose for COVID-19 immunisation. Medical history included diabetes and high blood pressure. The patient was not allergic to medications, food, or other products. Concomitant medications included insulin (MANUFACTURER UNKNOWN) taken for unknown indication from unspecified date, unknown if ongoing. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 14Apr2021 at 20:00, the patient experienced hives on chest, left arm and stomach, with some itchiness on the arm. These events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were taken as a result of the events which included treatment with application of cooling ointment on skin. The clinical outcome of the events hives and itchiness were resolved on an unknown date in Apr2021. No follow-up attempts are possible. No further information is expected.

Other Meds: INSULIN

Current Illness:

ID: 1673706
Sex: F
Age:
State: CA

Vax Date: 04/06/2021
Onset Date: 04/11/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: I am having vaginal bleeding, started with spotting on 11Apr, turned to mostly bright red blood on 12Apr, heavier on 13Apr, no change on 14Apr; This is a spontaneous report from a contactable consumer or other non-healthcare professional (patient herself). A 58-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EW0153), dose 1 via an unspecified route of administration, administered in Arm Left on 06Apr2021 15:00 (03:00 pm) as dose 1, single (at age of 58-years old) for covid-19 immunization. The patient's medical history included known allergies: allergic to sulfa drugs and patient had an adverse reaction to Non-steroidal anti-inflammatory drugs (NSAIDs). The patient had menopausal. The patient's concomitant medication/other medications in two weeks included unspecified medication. The patient had no other vaccine in four weeks. The patient had no covid prior vaccination. The patient was not covid tested post vaccination. The patient stated, she was post-menopausal. She was having vaginal bleeding, started with spotting on 11Apr2021, turned to mostly bright red blood on 12Apr2021, heavier on 13Apr2021, no change on 14Apr2021 (today). The event resulted in doctor or other healthcare professional office/clinic visit. The patient not received treatment for the adverse event. The outcome of the event was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1673707
Sex: F
Age:
State: NY

Vax Date: 04/16/2021
Onset Date: 04/17/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: My hands and fingers ache really bad; My hands and fingers ache really bad; Have a burning sensation; This is a spontaneous report from a contactable consumer, the patient. A 71-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 16Apr2021 at 11:00 (at the age of 71-years-old) as a single dose for COVID-19 immunisation. The medical history included aortic valve replacement, asthma, celiacs and allergy to penicillin. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. The concomitant medications included amlodipine (MANUFACTURER UNKNOWN), losartan potassium (LOSARTIN), levothyroxine (MANUFACTURER UNKNOWN), folic acid (MANUFACTURER UNKNOWN) and vitamin d nos (MANUFACTURER UNKNOWN), all from unknown dates and for unspecified indications. On 17Apr2021, the patient's hands and fingers ache really bad and had a burning sensation. Therapeutic measures were not taken as a result of the reported events. The adverse events did not result in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events hands and fingers ache really bad and had a burning sensation was not recovered at the time of this report. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: AMLODIPINE; LOSARTIN; LEVOTHYROXINE; FOLIC ACID; VITAMIN D NOS

Current Illness:

ID: 1673708
Sex: F
Age:
State: OH

Vax Date: 04/17/2021
Onset Date: 04/18/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Headache, Heart rate increased, Injection site erythema, Injection site pain, Injection site swelling

Symptoms: Lump on left side of collarbone ( lymph node).; This is a spontaneous report from a contactable consumer, the patient. A 55-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0153) via an unspecified route of administration in the left arm on 17Apr2021 at 10:15 (at the age of 55-years-old) as a single dose for COVID-19 immunisation. Medical history was not reported. The patient was not allergic to medications, food, or other products. The patient received unspecified medications within 2 weeks of vaccination. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8730) via an unspecified route of administration in the left arm on an unknown date in Mar2021 at 10:30 (at the age of 55-years-old) as a single dose for COVID-19 immunisation. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the vaccination. On 18Apr2021 at 17:00, the patient experienced lump on left side of collarbone (lymph node).The event did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. It was unknown whether any therapeutic measures were taken as a result of the event. The clinical outcome of the event lump on left side of collarbone (lymph node) was not resolved at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1673709
Sex: M
Age:
State: IL

Vax Date: 03/17/2021
Onset Date: 03/17/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: Probably after 12 hours, veins/nerves started pulling up near shoulder and jaws; Probably after 12 hours, veins/nerves started pulling up near shoulder and jaws; This is a spontaneous report from a contactable consumer, the patient. A 50-year-old male patient received unknown dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 17Mar2021 at 08:45 (at the age of 50-years-old) as a single dose for COVID-19 immunisation. Medical history included none. The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Concomitant medications included fenofibrate (MANUFACTURER UNKNOWN) and simvastatin (MANUFACTURER UNKNOWN) all from an unknown date from an unspecified indication. On 17Mar2021 at 20:00, the patient experienced probably after 12 hours, veins/nerves started pulling up near shoulder and jaws. Patient stated that he took a hot shower and slept, when he woke up after 4 hours, it became much better. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events probably after 12 hours, veins/nerves started pulling up near shoulder and jaws was recovered on an unspecified date in 2021. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: FENOFIBRATE; SIMVASTATIN

Current Illness:

ID: 1673710
Sex: F
Age:
State: TX

Vax Date: 03/18/2021
Onset Date: 03/19/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 20210408; Test Name: SARS-CoV-2 PCR test; Test Result: Negative ; Comments: Nasal Swab

Allergies:

Symptom List: Injection site pain

Symptoms: Hive like bumps on face (mainly around the forehead and cheeks), on chest,; and a little bit around the site of the shot; This is a spontaneous report from a non-contactable consumer, the patient. A 28-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6208) via an unspecified route of administration in the left arm on 18Mar2021 at 14:15 (at the age of 28-years-old) as a single dose for COVID-19 immunisation. Medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. The patient did not receive any other medication within two weeks of vaccination. On 19Mar2021 at 07:00, the patient experienced hive like bumps on face (mainly around the forehead and cheeks), on chest, and a little bit around the site of the shot. No therapeutic measures were taken as a result of the event. Since the vaccination, the patient had been tested for COVID-19. On 08Apr2021, the patient gave nasal swab for SARS-CoV-2 PCR test and the result was negative. The clinical outcome of the event hive like bumps on face (mainly around the forehead and cheeks), on chest, and a little bit around the site of the shot was recovered on an unknown date in 2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1673711
Sex: M
Age:
State: GA

Vax Date: 04/12/2021
Onset Date: 04/15/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site induration, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: Small lump under skin in back of neck left side; This is a spontaneous report from a contactable consumer, the patient. A 64-year-old male patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0162) via an unspecified route of administration in the arm left on 12Apr2021 at 12:30 (at the age of 64-years-old) as a single dose for COVID-19 immunisation. The patient did not have any relevant medical history. The patient had no known allergies .The patient did not receive any medication within two weeks of vaccination. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8727) via an unspecified route of administration in the left arm on 22Mar2021 at 11:00 (at the age of 64-years-old) as a single dose for COVID-19 immunisation. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 15Apr2021 the patient experienced small lump under skin in back of neck left side. Therapeutic measures were not taken as a result of the event. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. The clinical outcome of the event small lump under skin in back of neck left side was not resolved at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1673712
Sex: M
Age:
State: ID

Vax Date: 03/16/2021
Onset Date: 03/16/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011j20a
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data: Test Date: 2021; Test Name: Hepatitis C antibody test (Anti-HCV screening); Result Unstructured Data: Test Result:False positive; Comments: Result was a false positive and did not show any reactivity to the anti-HCV test.; Test Date: 2021; Test Name: Hepatitis C antibody test (Anti-HCV screening); Result Unstructured Data: Test Result:Reactive result; Comments: Had a reactive result on the anti-HCV screening

Allergies:

Symptom List: Chills, Dizziness, Nausea, Pain, Tachycardia

Symptoms: A very slight headache starting approximately 4 hours post vaccination.; This is a spontaneous report from a contactable consumer, the patient. A 50-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: CN6206) via an unspecified route of administration in the right arm on 16Mar2021 (at the age of 50-years-old) as a single dose for COVID-19 immunisation. The patient did not have any relevant medical history. The patient had no known allergies to medications, food or other products. Concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 16Mar2021 at 16:00, approximately 4 hours post vaccination, the patient experienced a very slight headache. Additionally on 20Mar2021, four days after vaccination, the patient donated blood, which was a regular occurrence for him. On an unknown date in 2021, he received word back from his donation that he had a reactive result on the anti-HCV screening. Extra testing indicated that this result was a false positive and that he did not show any reactivity to the anti-HCV test. The event did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Therapeutic measures were not taken as a result of the event. The clinical outcome of the event slight headache was resolved on an unknown date in 2021. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1673713
Sex: M
Age:
State: IL

Vax Date: 04/15/2021
Onset Date: 04/15/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: Blurred vision; This is a spontaneous report from a contactable consumer, the patient. A 59-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 15Apr2021 at 12:15 (at the age of 59-year-old) as a single dose for COVID-19 immunisation. Medical history included hypertension. The patient had no known allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included lisinopril (MANUFACTURER UNKNOWN) and dronedarone hydrochloride (MULTAQ). On 15Apr2021 at 12:45, the patient experienced blurred vision. The event resulted in doctor or other healthcare professional office/clinic visit. Since the vaccination, the patient had not been tested for COVID-19. Therapeutic measures were not taken as a result of the event. The clinical outcome of the event blurred vision was not resolved at the time of this report. No follow-up attempts are required; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: LISINOPRIL; MULTAQ

Current Illness:

ID: 1673714
Sex: F
Age:
State: SC

Vax Date: 04/09/2021
Onset Date: 04/09/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: Terrible headache; Fatigue; This is a spontaneous report from a contactable consumer, the patient. A 44-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the right arm on 09Apr2021 at 12:15 (at the age of 44-years-old) as a single dose for COVID-19 immunisation. Medical history included Rheumatoid Arthritis (RA) and posterior uveitis. The patient was allergic to penicillin. Concomitant medications included omeprazole (MANUFACTURER UNKNOWN), lisinopril (MANUFACTURER UNKNOWN), metoprolol (MANUFACTURER UNKNOWN) and rosuvastatin calcium (CRESTOR) all were from unknown date and for unspecified indication. The patient previously took doxycycline (MANUFACTURER UNKNOWN), ciprofloxacin (MANUFACTURER UNKNOWN) and experienced drug allergy. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the right arm on 19Mar2021 at 12:15 (at the age of 43-years-old) as a single dose for COVID-19 immunisation. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 09Apr2021 at 15:00, after the second dose of vaccination the patient experienced terrible headache and fatigue. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were not taken as the result of adverse events. The clinical outcome of the events terrible headache and fatigue were not recovered at the time of report. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: OMEPRAZOLE; LISINOPRIL; METOPROLOL; CRESTOR

Current Illness:

ID: 1673715
Sex: M
Age:
State: MD

Vax Date: 04/15/2021
Onset Date: 04/19/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: UNK
Manufacturer: UNKNOWN MANUFACTURER
Vax Name: VACCINE NOT SPECIFIED (NO BRAND NAME)
Lot:
Dose Series: UNK
Vax Route: SYR
Vax Site: UN

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site induration, Injection site pruritus, Injection site swelling, Myalgia

Symptoms: Sore arm - 4 days after injection; Sore shoulder - 4 days after injection; This is a spontaneous report received from a contactable consumer, the patient. A 56-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EW0161) via an unspecified route of administration in the left arm on 15Apr2021 at 11:00 (at the age of 56-years-old) as a single dose for COVID-19 immunisation. Medical history of the patient included diabetes. The patient did not had any allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included metformin (MANUFACTURER UNKNOWN) for unknown indication from unknown date and unknown if ongoing. The patient did not receive any other vaccine within four weeks prior to the COVID vaccine. On 19Apr2021, the patient had sore arm and shoulder 4 days after injection. No therapeutic measures were taken as a result of the reported events. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic, emergency room/department or urgent care. The clinical outcome of the events sore arm and shoulder were not resolved at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds: METFORMIN

Current Illness:

ID: 1673716
Sex: F
Age:
State: FL

Vax Date: 04/17/2021
Onset Date: 04/18/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Cough, Limb discomfort, Pain, SARS-CoV-2 test positive

Symptoms: "Swollen limpth nodes"; Burning mouth; Legs hurt below knee; Headache; Body felt like heavy/led; Very tired; Arm muscle hurts; Under arm the gland is very tender.; This is a spontaneous report from a contactable consumer, the patient. A 75-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0158) via an unspecified route of administration in the right arm on 17Apr2021 at 09:15 (at the age of 75-years-old) as a single dose for COVID-19 immunisation. The patient had no medical history. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient received unspecified medications within two weeks prior to the COVID-19 vaccination. The patient previously received codeine (MANUFACTURER UNKNOWN) and experienced a drug allergy. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8730) via an unspecified route of administration in the right arm on an unknown date as a single dose for COVID-19 immunisation. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccination. On 18Apr2021 at 08:30, the patient experienced "swollen limpth nodes", burning mouth, her legs hurt below the knee, headache, "body felt like heavy/led", very tired, her arm muscle hurt and she reported that she was on the third day after vaccine and was still tired and under arm the gland was very tender. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events "swollen limpth nodes", burning mouth, legs hurt below knee, headache, "body felt like heavy/led", very tired, arm muscle hurts and under arm the gland was very tender were not resolved at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1673717
Sex: F
Age:
State: TX

Vax Date:
Onset Date: 03/28/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 20210329; Test Name: Body temperature; Result Unstructured Data: Test Result:101

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: Vomiting; Fever (101); Muscle aches; Chills; Light headedness; Nausea; This is a spontaneous report from a contactable consumer, the patient. A 31-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL9263) via an unspecified route of administration in the left arm on 28Mar2021 at 10:15 (at the age of 31-year-old) as a single dose for COVID-19 immunisation. The patient had no medical history. The patient did not have any allergies to medications, food, or other products. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included escitalopram oxalate (LEXAPRO) and birth control (MANUFACTURER UNKNOWN) taken from unknown date for unknown indication. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 28Mar2021 the patient experienced light headedness and nausea right after vaccine, after about 36 hours later on 29Mar2021 patient started vomiting. The patient also had a fever 101(unspecified units), muscle aches and chills. On 29Mar2021 patient checked her body temperature and it was 101 (unspecified units). Therapeutic measures were not taken as a result of the events. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events light headedness, nausea were resolved on unknown date in 2021. The clinical outcome of the events fever 101(unspecified units), muscle aches and chills were resolved on 02Apr2021. The clinical outcome of the event vomiting was resolved on an unknown date in Mar2021. No follow-up attempts are needed. No further information is expected.

Other Meds: LEXAPRO

Current Illness:

ID: 1673718
Sex: F
Age:
State: NJ

Vax Date: 04/06/2021
Onset Date: 04/01/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pain, Injection site swelling

Symptoms: Ringing in my ears\a high pitched sound like the zing of a high tension wire; Physical sensation; This is a spontaneous report from a contactable consumer, the patient. A 63-year-old non-pregnant female patient received unknown dose number of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0150) via an unspecified route of administration in the left arm on 06Apr2021 at 10:45 (at the age of 63-year-old) as a single dose for COVID-19 immunisation. Medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any concomitant medications within 2 weeks of vaccination. The patient previously received ampicillin and experienced drug allergy. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. On an unknown date in Apr2021 the patient experienced ringing in ears-a high pitched sound like the zing of a high tension wire and she clapped hands and her left ear rang loudly, which was both a sound and a physical sensation. Since the vaccination, the patient had not been tested for COVID-19. The adverse event did not result in doctor or other healthcare professional office or clinic visit and emergency room or department or urgent care. No therapeutic measures were taken as a result of the reported events. The clinical outcome of the events ringing in ears and physical sensation were not recovered at the time of report. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1673719
Sex: F
Age:
State: NJ

Vax Date: 04/07/2021
Onset Date: 04/11/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EK9231
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chills, Feeling cold, Feeling hot, Myalgia, Pain

Symptoms: Started seeing blisters; Diagnosed with shingles by the typical skin presented in lower abdomen, right side of the waist and the back area at waist level; More and larger red rash surfaced; felt burning on the skin in lower abdomen; Fatigue; This is a spontaneous report from a contactable consumer, the patient. A 59-year-old female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8729) via an unspecified route of administration in the left arm on 07Apr2021 at 12:00 (at the age of 59-years-old) as a single dose for COVID-19 immunisation. Medical history included a mild degree of diabetes which was under control and the patient had no autoimmune diseases, was a non-smoker and was not an alcohol user. The patient had no allergies to medications, food, or other products. Concomitant medications included metformin (MANUFACTURER UNKNOWN) taken from an unknown date. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 11Apr2021 at 20:00, after the first dose, the patient felt burning on the skin in lower abdomen with fatigue. On 12Apr2021 and 13Apr2021, the following 2 days, the affected areas grew wider and spread to the right and her back; more and larger red rash surfaced. On 14Apr2021, the patient started seeing blisters, so went to see a doctor, and told her it might have resulted from the first dose. On 14Apr2021, the patient was diagnosed with shingles by the typical skin presented in lower abdomen, right side of the waist and the back area at waist level. The events resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of events and included treatment with valacyclovir 1 gm three times a day for seven days. On 15Apr2021, the patient read an Israel report which came up indicating shingles events having a possible link to the vaccine and the patient wanted to know if she could skip the second dose which was scheduled on 05May2021. Her shingles would not be fully recovered before the second dose and she wanted to know what was the maximum interval allowed between dose 1 and dose 2 to maintain the desired efficacy. She also asked if skipping the second dose would impact Pfizer upcoming variants boost dose on efficacy. She also asked if she can receive other company's second dose or a booster if she planned to skip Pfizer's second dose. The clinical outcome of the events burning on the skin in lower abdomen with fatigue, red rash, blisters and shingles were not resolved at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds: METFORMIN

Current Illness:

ID: 1673720
Sex: F
Age:
State: NJ

Vax Date: 04/17/2021
Onset Date: 04/19/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: Hives; Fatigue; Ringing in ears; This is a spontaneous report from a contactable consumer, the patient. A 54-year-old non-pregnant female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0162) via an unspecified route of administration in the left arm on 17Apr2021 at 02:45 (at the age of 54-years-old) as a single dose for COVID-19 immunisation. The patients' medical history included allergy to nuts. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccination. Concomitant medications included levothyroxine sodium (SYNTHROID), esomeprazole (NEXIUM), sertraline hydrochloride (ZOLOFT), atorvastatin calcium (LIPITOR) and fexofenadine hydrochloride (ALLEGRA); all for unknown indications from unknown dates and unknown if ongoing. On 19Apr2021 at 02:30, the patient experienced hives, fatigue and ringing in ears. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. Therapeutic measures were not taken as a result of the events. The clinical outcome of the events hives, fatigue and ringing in ears were resolving at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds: SYNTHROID; ESOMEPRAZOLE; ZOLOFT; LIPITOR; ALLEGRA

Current Illness:

ID: 1673721
Sex: F
Age:
State: MA

Vax Date: 04/17/2021
Onset Date: 04/18/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 2
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Abnormal behaviour, Adverse reaction, Anger, Asthma

Symptoms: Feeling tired; Upper body aches; Headache; This is a spontaneous report from a contactable consumer, the parent. A 16-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the right arm on 17Apr2021 at 11:00 (at the age of 16-years-old) as a single dose for COVID-19 immunisation. The patient did not have any relevant medical history. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Patient did not receive any other medication within two weeks of vaccination. The patient had no allergies to medications, food, or other products. The patient previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration on 27Mar2021 at 11:15 (at the age of 16-years-old) as a single dose for COVID-19 immunisation. On 18Apr2021 at 12:00, the patient experienced feeling tired, upper body aches and headache. The events did not result in doctor or other healthcare professional office or clinic visit and emergency room or department or urgent care. Therapeutic measures were taken as a result of feeling tired, upper body aches and headache and included treatment with ADVIL from an unknown start date to an unknown stop date. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events feeling tired, upper body aches and headache were recovering at the time of this report. No follow-up attempts are needed; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1673722
Sex: M
Age:
State: NY

Vax Date: 04/01/2021
Onset Date: 04/19/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Consciousness fluctuating, Crying, Dry skin, Epistaxis, Headache

Symptoms: sore shoulder; This is a spontaneous report from a contactable consumer. A 46-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration on an unknown date in Apr2021 (at the age of 46-years-old) as a single dose for COVID-19 immunisation. Medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. It was unknown if patient receive any other vaccines within four weeks prior to the COVID vaccine. Concomitant medications were not reported. On 19Apr2021 at 09:11, the patient experienced sore shoulder. The patient did not receive any treatment for the event. Since the vaccination, it was unknown if the patient had been tested for COVID-19. The clinical outcome of the event shoulder soreness was recovered on an unknown date in 2021. No follow-up attempts are needed; information about lot/batch number cannot be obtained; no further information is expected.

Other Meds:

Current Illness:

ID: 1673723
Sex: M
Age:
State: CO

Vax Date: 03/20/2021
Onset Date: 03/28/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Hypotonia, Lethargy, Respiratory rate decreased, Screaming, Skin warm

Symptoms: Fingers on both hands are blue and are painful.; Fingers on both hands are blue and are painful; Left leg swollen; Fingers on both hands are blue and are painful. No feeling; This is a spontaneous report from a contactable consumer, the patient. A 45-year-old male patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EP6955) via an unspecified route of administration in the left arm on 20Mar2021 (at the age of 45-years-old) as a single dose for COVID-19 immunisation and received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: ER8731) via an unspecified route of administration in the right arm on 10Apr2021 (at the age of 45-years-old) as a single dose for COVID-19 immunisation. Medical history included human immunodeficiency virus (HIV). The patient had no known allergies to food, medication or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications were not reported. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 28Mar2021, the patient experienced fingers on both hands were blue and were painful, no feeling and left leg was swollen. The events resulted in doctor or other healthcare professional office/clinic visit. It was unknown whether any therapeutic measures were taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events fingers on both hands were blue and were painful, no feeling and left leg was swollen was not recovered at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1673724
Sex: F
Age:
State: MI

Vax Date: 04/01/2021
Onset Date: 04/14/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 026LZOA
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data: Test Date: 20210417; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptom List: Vomiting

Symptoms: Headaches; little bit of congestion; sore throat; body aches; This is a spontaneous report from a contactable consumer, the patient. A 31-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EP7534) via an unspecified route of administration in the right arm on 01Apr2021 (at the age of 31-years-old) as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient had no known allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 14Apr2021, the patient experienced headaches, little bit of congestion, sore throat and body aches. The events resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures were not taken as a result of the events. On 17Apr2021, the patient underwent COVID-19 PCR, nasal swab test and the result was negative. Since the vaccination, the patient had been tested for COVID-19. The clinical outcome of the events headaches, little bit of congestion, sore throat and body aches was unknown at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1673725
Sex: F
Age:
State: MI

Vax Date: 04/13/2021
Onset Date: 04/13/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: elevated heart rate occurred/ notice additional elevated heart rate occurring while just sitting; body aches and soreness with continual nerve twitches thru-out body: neck, back, calves and right hand fore finger/ sharpness of needle like pain in calves, fore finger, neck and back; Pinch nerve with tingling in right hand forefinger, back, neck and legs (calves)/ with continual nerve twitches thru-out body: neck, back, calves and right hand fore finger; sharp pinch in neck; slight dizziness (1 hour afterward); headache; sore arm in left (injection site); tingle right finger/ Pinch nerve with tingling in right hand forefinger, back, neck and legs (calves)/ continual tingles in neck, back, calves; This is a spontaneous report from a contactable consumer, the patient. A 53-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EW0158) via an unspecified route of administration in the left arm on 13Apr2021 at 09:00 (at the age of 53-year-old) as a single dose for COVID-19 immunisation. Medical history was reported as none. The patient had no allergies to medications, food, or other products. The patient did not take any concomitant medications. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 13Apr2021 at 11:00, the patient experienced at slight dizziness (1 hour afterward) headache, sore arm in left (injection site), sharp pinch in neck and tingle right finger. On 14Apr2021 the patient experienced pinch nerve with tingling in right hand forefinger, back, neck and legs (calves). On 15Ap2021 and 16Apr2021 she had continual tingles in neck, back, calves. On 17Apr2021 patient had elevated heart rate, body aches and soreness with continual nerve twitches thru-out body, neck, back, calves and right-hand fore finger. On 18Apr2021 she noticed additional elevated heart rate occurring while just sitting, same symptoms, sharpness of needle like pain in calves, fore finger, neck and back. Therapeutic measures were not taken as a result of the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event slight dizziness (1 hour afterward) headache, sore arm in left (injection site), sharp pinch in neck and tingle right finger, pinch nerve with tingling in right hand forefinger, back, neck and legs (calves), continual tingles in neck, back and calves, elevated heart rate, body aches and soreness with continual nerve twitches thru-out body, neck, back, calves and right-hand fore finger and additional elevated heart rate occurring while just sitting, same symptoms, sharpness of needle like pain in calves, fore finger, neck and back was not resolved at the time of reporting. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1673726
Sex: F
Age:
State: ME

Vax Date: 04/06/2021
Onset Date: 04/15/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Back pain, Cold sweat, Headache, Nausea, Vomiting

Symptoms: Red spots on stomach and upper front of body; This is a spontaneous report from a contactable consumer, the patient. A 53-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration in the left arm on 06Apr2021 at 12:30 (at the age of 53-year-old) as a single dose for COVID-19 immunisation. Medical history included high allergic reaction to poison Ivy exposure. The patient previously received paracetamol (TYLENOL) on an unspecified date for an unknown indication and experienced drug allergy. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included losartan (MANUFACTURER UNKNOWN) from an unknown date, for unknown indication. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 15Apr2021 (Thursday) at 05:00, the patient woke up with lots of red spots on stomach and upper front of body. No therapeutic measures were taken as a result of the event. Since the vaccination, the patient had not been tested for COVID-19. The events did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. The clinical outcome of the event red spots on stomach and upper front of body was recovering at the time for this report. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: LOSARTAN

Current Illness:

ID: 1673727
Sex: F
Age:
State: WI

Vax Date: 02/19/2021
Onset Date: 02/27/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025j20-2A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: This is a spontaneous report from a contactable nurse. An 89-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL3249) 0.3 mL via intramuscular route of administration in the left arm on 19Feb2021 (at the age of 89-years-old) as a single dose for COVID-19 immunisation. Medical history included Congestive Heart Failure (CHF), tricuspid and mitral valve regurgitation, hyperlipidemia, hypertension, Gastroesophageal Reflux Disease (GERD), osteopenia, chronic dorsalgia, chronic lumbago, left partial lobectomy related to blastomycosis in 1967 and hysterectomy. The patient was allergic to iodine contrast media and iodine containing multivitamin. Concomitant medications included paracetamol (ACETAMINOPHEN), amitriptyline (MANUFACTURER UNKNOWN), butalbital, caffeine, paracetamol (FIORICET), colecalciferol, calcium phosphate (CALCIUM+D), hydrocodone, paracetamol (APAP;HYDROCODONE), furosemide (MANUFACTURER UNKNOWN), meloxicam (MANUFACTURER UNKNOWN), metoprolol (MANUFACTURER UNKNOWN), omeprazole (MANUFACTURER UNKNOWN), iron (MANUFACTURER UNKNOWN), potassium (MANUFACTURER UNKNOWN), simvastatin (MANUFACTURER UNKNOWN), cyanocobalamin (VITAMIN B12), senna alexandrina (SENNA) and multivitamins (MANUFACTURER UNKNOWN), all the above taken daily and alendronate sodium (FOSAMAX), taken once weekly; all the medications were taken for unspecified indications from unknown dates. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 27Feb2021, after the second immunisation, the patient experienced zoster rash left mid T-spine, wrapping to under axilla and under breast. Care required 4 weekly visits and antibiotic, until rash was resolved. The event resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of the event and included treatment with lidoderm pain patch; cellulitis occurred under patch/zoster which included treatment with oral antibiotic and monitoring. The clinical outcome of the event zoster rash was resolved on an unknown date in 2021. No follow-up attempts are needed. No further information is expected.

Other Meds: ACETAMINOPHEN; AMITRIPTYLINE; FIORICET; CALCIUM+D; APAP;HYDROCODONE; FUROSEMIDE; MELOXICAM; METOPROLOL; OMEPRAZOLE; IRON; POTASSIUM; SIMVASTATIN; VITAMIN B12 [CYANOCOBALAMIN]; FOSAMAX; SENNA [SENNA ALEXANDRINA]

Current Illness:

ID: 1673728
Sex: F
Age:
State: CA

Vax Date: 04/17/2021
Onset Date: 04/17/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Diarrhoea, Fatigue, Feeling abnormal, Headache

Symptoms: Chills; Fever; Headache; Body aches; Nausea; This is a spontaneous report from a contactable consumer, the patient. A 53-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, lot number: EW0170) via an unspecified route of administration in the left arm on 17Apr2021 at 08:30 (at the age of 53-year-old) as a single dose for COVID-19 immunisation. Medical history included thyroid disorder and high blood pressure. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Concomitant medications included levothyroxine (MANUFACTURER UNKNOWN) started on an unknown date for thyroid disorder and unknown if ongoing. The patient previously took metoprolol (MANUFACTURER UNKNOWN) started on an unknown date for unknown indication and experienced drug allergy. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, lot number: ER8732) via an unspecified route of administration in the left arm on 27Mar2021 at 15:30 (at the age of 53-year-old) as a single dose for COVID-19 immunisation. On 17Apr2021 at 20:30, about 12 hours after injection, the patient experienced chills, fever, headache, body aches and nausea. The events did not result in doctor or other healthcare professional office or clinic visit, emergency room or department or urgent care. No therapeutic measures were taken as a result of the reported events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the events chills, fever, headache, body aches and nausea were recovering at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds: LEVOTHYROXINE

Current Illness:

ID: 1673729
Sex: F
Age:
State: KS

Vax Date: 04/01/2021
Onset Date: 04/03/2021
Rec V Date: 09/04/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Hot flush, Myalgia, Nausea, Tension headache

Symptoms: Under my left arm (where got shot) swelled to big enough size. would say it was as big as golf ball and assuming it was a lymph node; Arm could not go straight down and it was very tender; Had a rash covered whole body for a full week. The sun seemed to aggravate the rash; It was a rash that itched; This is a spontaneous report from a contactable consumer, the patient. A 64-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FP 7533) via an unspecified route of administration in the left arm on 01Apr2021 at 16:15 (at the age of 64-year-old) as a single dose for COVID-19 immunisation. Medical history included latex allergy and COVID-19. The patient previously took amoxicillin (MANUFACTURER UNKNOWN) on an unknown date and experienced drug allergy. Prior to vaccination, the patient was diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 03Apr2021 at 06:00, after 24 hours of vaccine, the patient experienced under left arm (where got shot) swelled to big enough size that arm could not go straight down and it was very tender. It was as big as golf ball and patient assumed it was a lymph node. Patient also had a rash covering her whole body for a full week. The sun seemed to aggravate the rash and it was a rash that itched. Therapeutic measures were taken as a result of the event rash and itchy rash and included treatment with BENADRYL. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event under left arm (where got shot) swelled to big enough size that arm could not go straight down and it was very tender, had a rash covering her whole body for a full week and it was a rash that itched was recovered on an unknown date in Apr2021. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am