VAERS 2021 Database www.vaers.hhs.gov

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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: 1792565
Sex: F
Age:
State: NC

Vax Date: 02/28/2021
Onset Date: 02/28/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 20210301; Test Name: slight fever; Result Unstructured Data: Test Result:<101.1; Comments: a slight fever, fever would come and go, it never got over 100.1

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: diarrhea; getting nauseated at my stomach; headache; nose started getting congestion / stuffy nose; coughing; sneezing; chills; a slight fever, fever would come and go, it never got over 100.1; feeling of tiredness/her "whole body as feeling yucky.; Itching started on my head, top of my head to my shoulders, face, eyes, ears, neck, itching scalp, the back of my neck was itching, never lower than my shoulders and I never actually broke out; I was sick for about 17 days; chest congestion; upset stomach; didn't have the strength to do nothing; felt horrible; This is a spontaneous report from a contactable consumer (patient) via medical information team. A 70-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN6202) via an unspecified route of administration, administered in Arm Left on 28Feb2021 at 13:30 (at the of 70-year-old) as dose 1, single for COVID-19 immunization.Medical history included chronic obstructive pulmonary disease (from 10 years), ongoing Severe rhinitis (forever), allergy (since she was 45 years old), muscle atrophy (due to hip replacement that the doctor botched in 2011 and 2013), seasonal allergy (really bad allergies and it is springtime with pollen ,Severe allergies in spring in summer and fall she have a tendency she can get severe sinusitis, rhinitis from the allergies, if that flares up it turns into bronchitis it turns to pneumonia).The patient did not had any other vaccine within 4 weeks prior to Covid-19 vaccine. Patient family medical history was reported as none.The patient previously took Zyrtec and experienced Hypersensitivity and took Prevagen for memory and it made her stupid.Concomitant medication included ongoing fluticasone furoate, vilanterol trifenatate (BREO ELLIPTA) taken for chronic obstructive pulmonary disease, respiratory tract infection (for 10 years; helps keep her bronchioles open); ongoing alprazolam taken for anxiety, panic attack; ongoing paroxetine taken for anxiety, panic attack; ongoing fexofenadine hydrochloride (ALLEGRA) taken for hypersensitivity(Allegra 180 twice a day and during spring and fall it still doesn't keep her allergies in check), ongoing colecalciferol (D3) taken for bone deformity(taking for 6 years can't walk well from the old hip surgery, and doesn't go outside much) and ongoing ascorbic acid, betacarotene, biotin, calcium, chloride, chromium, copper, folic acid, iodine, iron, magnesium, manganese, molybdenum, nickel, nicotinic acid, pantothenic acid, phosphorus, potassium, pyridoxine hydrochloride, riboflavin, selenium, silicon, thiamine, vanadium, vitamin b12 nos, vitamin d nos, vitamin e nos, vitamin k nos, xantofyl, zinc (CENTRUM SILVER WOMEN 50+) taken for an unspecified indication. On 28Feb2021 at 21:30 the patient experienced Itching all over, On 01Mar2021 Nose congestion, Coughing, Sneezing, Chills, Fever and Tiredness, On 03Mar2021, the patient had headache, On 08Mar2021, the patient experienced nauseated, On 09Mar2021, the patient had diarrhea and On unknown date in 2021 the patient experienced Respiratory tract congestion, upset stomach, Weakness, Feeling abnormal, she was sick for about 17 days. It was reported within 8 hours of taking the shot she started itching. Itching started on my head, top of my head to my shoulders, face, eyes, ears, neck, itching scalp, the back of my neck was itching, never lower than my shoulders and I never actually broke out and that that itching so bad that she was digging the skin off and was raw in the places where she dug. She used back scratcher to scratch her head. She didn't have any Benadryl at the house to take. She ended up taking an Allegra 180mg. She fell asleep about 04:00 am that morning. Then next morning 01MAR2021, she was still itching and it was time to take her morning medication and that includes an Allegra at 06:00 am so she took the morning medications including the Allegra. About three or four hours after that, it started subsiding. Then after that subsided, then her nose started getting congestion, she was coughing sneezing and she started getting a headache. The nasal congestion, still have that, could be coming from my sinuses could be an allergy overlap. she had a lot of chest congestion. The itching stopped later that day. The cough, sneezing and nasal congestion however are still ongoing. Stated she has severe reactions to medications and she's not sure if these adverse reactions are her allergies overlapping with side effects of the shot. She started to have a headache in her temples, top of her head, eyes and to behind her ear into her neck on the left-hand side which lasted for three days. Adds it hurt so bad she couldn't open her eyes. Then she had started getting nauseated at stomach, upset stomach and then started with the diarrhea(lasted for another 2 days). This all occurred within a 17-day period. she did not have it all at one time, some overlapped, and some didn't. During the whole period of time, her whole body, she didn't have the strength to do nothing. she felt horrible. The 3rd week of March, she had chills and fever (that ranged between 99.8 F- 100.2 F), it never got over 100.1 But this all lasted for 17-18 days. She says it would come and go. She also felt an overall feeling of tiredness, her whole body as feeling yucky with multiple days that she didn't get out of bed except to go to the bathroom. Just this past week, she was having to deal with the coughing and stuffy nose, sneezing and all of that stuff, which was normal because of her allergies. She was scheduled to have her second dose on 28Mar2021 but she has not had it. She wants to know should she take the second dose because she heard the side effects for the second dose are worse. Stated she couldn't remember better and once woke up at 05:30 am and told her son to let the dog out before he went to bed and it was morning time. The patient underwent lab tests which included body temperature: <101.1 (a slight fever would come and go it never got over 100.1) on 01Mar2021. Patient received treatment for the event pruritus with 2 allergy pills. Outcome of the events nasal congestion, coughing, sneezing, headache was resolving, Event pruritus resolved on 01Mar2021,Nausea resolved on 10Mar2021; diarrhea resolved on 11Mar2021 and Chills, Pyrexia resolved on 07Mar2021,fatigue resolved on 15Mar2021, and outcome of the other events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: BREO ELLIPTA; ALPRAZOLAM; PAROXETINE; ALLEGRA; D3; CENTRUM SILVER WOMEN 50+

Current Illness: COPD (from 10 years); Rhinitis (forever)

ID: 1792566
Sex: M
Age:
State:

Vax Date: 03/24/2021
Onset Date:
Rec V Date: 10/16/2021
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: breaking out in hives, in my lip, top lip first then it went to my bottom lip around the injection site and on my butt; breaking out in hives, in my lip, top lip first then it went to my bottom lip around the injection site and on my butt; This is a spontaneous report from a contactable consumer (patient) or other non-health care professional. A 81-year-old male patient received bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: ER8732) via an unspecified route of administration on 24Mar2021, last wednesday (at the age of 81-year-old) as dose 2, single for covid-19 immunization. Medical history included hives, he had these hives when he was a kid, 75 years ago from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. Historical vaccine included BNT162B2 (solution for injection) via an unspecified route of administration, administered on an unspecified date, as dose 1 single for COVID-19 immunization. On an unspecified date in 2021, past few days the patient experienced breaking out in hives, in his lip, top lip first then it went to his bottom lip around the injection site and on his butt. He was calling to report this. Should he take something, or should he call his doctor. Had anything like this been reported before. Caller wanted to know how long this report was going to take. He wants to be transferred over to get his question answered. Outcome of the events were unknown. No follow-up attempts are possible. No further information is expected. Follow-up attempts not completed; information about lot/batch number cannot be obtained. No further information expected.

Other Meds:

Current Illness:

ID: 1792567
Sex: F
Age:
State: TX

Vax Date: 03/06/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: Test Date: 20210222; Test Name: Blood work; Result Unstructured Data: Test Result:Unknown results; Test Name: several tests; Result Unstructured Data: Test Result:No findings.; Comments: they did X-ray, they give lab work they give several test like strep, mono and susceptibility in the case of rash, they can't find anything as of yesterday, and they can't find anything.; Test Name: X ray; Result Unstructured Data: Test Result:No findings.; Comments: they did X-ray, they give lab work they give several test like strep, mono and susceptibility in the case of rash, they can't find anything as of yesterday, and they can't find anything.

Allergies:

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

Symptoms: I have a dry hacking cough; Chills; I start developing rash with itching and at the same time the sore throat came back; I start developing rash with itching and at the same time the sore throat came back; developing a sore throat; Extreme fatigue within 2 hours of second shot and was down to the bed I was just so tired I couldn't held my head up; my lymph node was swollen after the second one I still have the nausea; my lymph node was swollen after the second one I still have the nausea; This is a spontaneous report from a contactable consumer (patient). A 68-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EN6202), via an unspecified route of administration, in right arm on 06Mar2021 (at the age of 68-years-old) as dose 2, single for COVID-19 immunization. Medical history included diabetes mellitus, blood pressure high and breast cancer in remission. Concomitant medications included glimepiride, glipizide, amlodipine besilate, lisinopril, levothyroxine sodium (LEVOXYL) and simvastatin. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number and expiry date not reported), via an unspecified route of administration, on 07Feb2021 (at the age of 68-years-old) as dose 1, single for COVID-19 immunization after which the patient experienced sore throat, nausea and sickness. The patient experienced a dry hacking cough on an unspecified date, a rash with itching and at the same time the sore throat that came back on 16Mar2021, swollen lymph node and nausea in Mar2021, chills on an unspecified date, extreme fatigue within 2 hours of second shot and had to lay down in the bed on 06Mar2021. The patient underwent lab tests and procedures which included blood test: unknown results on 22Feb2021, X-ray, tests like strep, mono susceptibility in the case of rash. Therapeutic measures taken as a result of the events included antibiotics including Zyrtec, cough syrup, hydroxyzine 10 mg and ondansetron 4 mg. The outcome of the event dry hacking cough and extreme fatigue was unknown, rash with itching, swollen lymph node and nausea was not recovered, sore throat was recovering and event chills was recovered on an unspecified date. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: GLIMEPIRIDE; GLIPIZIDE; AMLODIPINE BESYLATE; LISINOPRIL; LEVOXYL; SIMVASTATIN

Current Illness:

ID: 1792568
Sex: U
Age:
State: MD

Vax Date: 03/24/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: arthritis in both my knees/ I have arthritis has gotten a zillion times worse; Cannot walk; Cannot stand up; Terrible pain/ excruciating pain; cannot straighten my leg; Started getting terrible pains in my joints; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number: EN6200, NDC number, UPC number and expiry date were reported as unknown) via an unspecified route of administration on 24Mar2021 as dose 1, single for covid-19 immunisation. Medical history included ongoing arthritis. The patient's concomitant medications were not reported. The patient is a senior citizen. The patient got the first dose of Pfizer covid vaccine on Wednesday i.e., on 24Mar2021. At night on 26Mar2021, patient's arm was better until at 9 o'clock, later the patient experienced terrible pain and started getting terrible pains in joints. The patient cannot stand up, can't walk, can't take a step, can't even get to the bathroom because can't straiten leg. It was not like this before the vaccine. The patient had arthritis in both knees from years but never had pain like this, so it had to come from the vaccine. The patient was in excruciating pain, everywhere the patient had arthritis had gotten a zillion times worse. The outcome of all the events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness: Knee arthritis

ID: 1792569
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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: body temperature; Result Unstructured Data: Test Result:Over 100 Fahrenheit

Allergies:

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

Symptoms: I woke up this morning with body aches and fever./ I woke up this morning with fever over 100, lot of body aches; I woke up this morning with body aches and fever./ I woke up this morning with fever over 100, lot of body aches; Lot of body aches, my arm is hurting real bad and left side of my neck; Lot of body aches, my arm is hurting real bad and left side of my neck; stomach cramps; This is a spontaneous report received from a contactable consumer (Patient herself). A (age: 67; unit: unknown) female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot number was not reported, Expiry Date: Unknown) via an unspecified route of administration on an unspecified date as dose number unknown, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. It was reported that Patient stated that she had a Pfizer vaccine yesterday 11:30 in the morning, and she had no symptoms at all. She woke up this morning with body aches and fever over 100, lot of body aches, stomach cramps, her arm was hurting real bad and left side of her neck where she has on that side. She has an appointment today 2:30 with dentist to have molar tooth extracted and she want to know if there any reason why she should not do that. The patient experienced, i woke up this morning with body aches and fever./ i woke up this morning with fever over 100, lot of body aches, my arm is hurting real bad and left side of my neck stomach cramps on an unspecified date. The patient underwent lab tests and procedures which included body temperature: over 100 Fahrenheit on an unspecified date. Outcome of all events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792570
Sex: F
Age:
State: KY

Vax Date: 03/27/2021
Onset Date: 03/28/2021
Rec V Date: 10/16/2021
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 Date: 20210330; Test Name: Xray of the Left hand; Result Unstructured Data: Test Result:Osteoarthritis of the thumb on her left hand

Allergies:

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

Symptoms: left hand swelled, Swelling moved to the right hand; couldn't sleep; Pain moved to her right shoulder, in the joint area/Pain then moved to her left shoulder same as what's in her right shoulder in the joint area; Left hand was sore when moving her fingers on 28MAR2021, the pain was terrific and she could hardly stand it, pain moved to the right hand not as severe as the left but very painful; By Tuesday 30MAR2021 her hand had swelled, the pain was terrific and she could hardly stand it, had some redness and it throbbed and ached.; This is a spontaneous report from a contactable consumer (patient). An 86-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE Solution for injection; lot number ERL613 and expiry date not reported), via an unspecified route of administration, administered in Arm Left on 27Mar2021 14:00 (at the age of 86-year-old), as dose 2, single, for COVID-19 immunisation. Medical history included Type 2 Diabetic which was diagnosed at 50 years old (so 36 years ago), AFib, High blood pressure, osteoarthritis. Concomitant medication included apixaban (ELIQUIS, 5mg, 1 tablet twice a day by mouth) taken for atrial fibrillation from Jul2020 and ongoing and a lot of heart medications. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE Solution for injection; lot number EN6205 and expiry date not reported), via an unspecified route of administration, administered in Arm Left on 06Mar2021 (at the age of 86-year-old), as dose 1, single, for COVID-19 immunization and was tired. No prior vaccinations within 4 weeks. History of other vaccinations included, other childhood immunizations; flu shot (Injection) in Left arm on Sep2020; pneumonia shot (1st shot) (Injection) in Left arm (was in her late 60's); pneumonia shot (2nd shot) (Injection) in Left arm (was in her late 70's); shingles vaccine (1st shot) (Injection) in Left arm (was in her late 70's); shingles vaccine (2nd shot) (Injection) in Left arm (was in her 70's), HIV Vaccine (1st shot) (Injection) in Left arm. On 28Mar2021 night, the patient left hand was sore when moving her fingers and thought maybe she injured the hand, but she did not fall or hit it on anything, and it was just sore. On 30Mar2021, the patient hand had swelled, the pain was terrific, and she could hardly stand it, had some redness and it throbbed and ached. It was reported that, the patient couldn't sleep from pain. On 30Mar2021, the swelling and pain moved to the right hand not as severe as the left but very painful and pain moved to her right shoulder, in the joint area. The patient took midol for pain. The patient went to doctor and took an X-ray of her left hand and diagnosed her with osteoarthritis of the thumb on her left hand which she already knew she had. The patient was diagnosed with osteoarthritis in her left hand before the COVID vaccine. The doctor said the patient could try the Tylenol and a cream Voltaren (Diclofenac Sodium 1 percent gel; Expiration: Nov2021, Lot: 2M2G). Then the hand cleared up and stopped aching in about 12 hours after taking with the Motrin and the Diclofenac. The patient took Motrin every 6-8 hours along with the gel every 6-8 hours. The Tylenol did nothing for her. It was reported that the pain was better but was still going on. The outcome for hand swelling and pain joints was not recovered, the outcome of couldn't sleep was unknown, outcome of pain in hand was recovering and the outcome of erythema was recovered. No follow-up attempts are needed. No further information is expected.

Other Meds: ELIQUIS

Current Illness:

ID: 1792571
Sex: F
Age:
State: SC

Vax Date: 02/17/2021
Onset Date:
Rec V Date: 10/16/2021
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: chills; fever; feeling unwell generally; almost like the flu; her left arm felt "a little bit sore; This is a spontaneous report from a contactable consumer (patient). A 69-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Lot number and Expiration date were not reported), via an unspecified route of administration (administered on the left arm) on 17Feb2021 as dose 1, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced her left arm felt "a little bit sore, chills, fever, feeling unwell generally and almost like the flu. It was reported that after first injection in her left arm, her left arm felt "a little bit sore, for about 2 days, had chills, fever, feeling unwell generally almost like the flu then it went away, in 3 or 4 days it was gone. The patient wanted to know how long does the protection last or is it only good for 6 months and may require a booster dose (3rd) in the future. The outcome of the events was recovered on an unspecified date. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792572
Sex: F
Age:
State: FL

Vax Date: 02/26/2021
Onset Date: 03/11/2021
Rec V Date: 10/16/2021
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: 202101; Test Name: Colonoscopy; Result Unstructured Data: Test Result:Good; Test Date: 202101; Test Name: Heart stress test; Result Unstructured Data: Test Result:Good; Test Date: 202101; Test Name: Mammogram; Result Unstructured Data: Test Result:Good; Test Date: 202101; Test Name: Ultrasound gallbladder; Result Unstructured Data: Test Result:Good; Test Date: 202101; Test Name: Different types of X-RAY; Result Unstructured Data: Test Result:Good

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: is still having lingering symptoms./now her immune system is angry and sometimes side effects last longer; now her immune system is angry and sometimes side effects last longer; she is feeling anxious; She thought her lymph nodes were swollen near her clavicle and up the neck and under her arm/swelling in lymph nodes under arm/swelling in lymph nodes in her neck and by her clavicle; swelling in lymph nodes in her neck and by her clavicle; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 50-year-old female patient received bnt162b2 (PIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EN6200; Expiration Date: Jun2021) via an unspecified route of administration, administered in arm left on 26Feb2021 (age at vaccination 50-year-old) as dose 2, single for covid-19 immunisation. The patient medical history included sarcoidosis from an unknown date and unknown if ongoing. She has been in remission for 25 years. The concomitant medications included LOSARTAN, AMLODIPINE BESILATE, COLECALCIFEROL (VITAMIN D [COLECALCIFEROL]), METFORMIN and METOPROLOL TARTRATE taken for an unspecified indication, start and stop date were not reported. Historic vaccine includes BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL9263) via an unspecified route of administration on 05Feb2021 (age at vaccination 50-year-old) as dose 1, single for COVID-19 immunisation. On an unspecified date, the patient experienced a is still having lingering symptoms /now her immune system is angry and sometimes side effects last longer, now her immune system is angry and sometimes side effects last longer, she is feeling anxious. On 11Mar2021, had swelling in lymph nodes in her neck and by her clavicle and she thought her lymph nodes were swollen near her clavicle and up the neck and under her arm/swelling in lymph nodes under arm/swelling in lymph nodes in her neck and by her clavicle. The patient did go to her primary care provider a couple of days ago because it has been lingering. The patient primary care provider said that the vaccine causes your immune system to be angry and that is what has caused the swelling and he thinks it will subside. The patient underwent lab tests and procedures which included colonoscopy, electrocardiogram, mammogram, ultrasound biliary tract, x-ray: good on Jan2021 prior to receiving the vaccine. The outcome of the events still having lingering symptoms/now her immune system is angry and sometimes side effects last longer, now her immune system is angry and sometimes side effects last longer, she is feeling anxious was unknown, the swelling in lymph nodes in her neck and by her clavicle was recovering and her lymph nodes were swollen near her clavicle and up the neck and under her arm/swelling in lymph nodes under arm/swelling in lymph nodes in her neck and by her clavicle was recovered on 31Mar2021. No follow-up attempts are possible. No further information is expected.

Other Meds: LOSARTAN; AMLODIPINE BESILATE; VITAMIN D [COLECALCIFEROL]; METFORMIN; METOPROLOL TARTRATE

Current Illness:

ID: 1792573
Sex: F
Age:
State: TX

Vax Date: 03/28/2021
Onset Date: 03/29/2021
Rec V Date: 10/16/2021
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: 20210329; Test Name: Fever; Result Unstructured Data: Test Result:99.5; Test Date: 20210330; Test Name: Fever; Result Unstructured Data: Test Result:over 102 up to 104.3; Test Date: 20210331; Test Name: Fever; Result Unstructured Data: Test Result:99.3

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: Severe aches all over; Migraine headache; Chills; Nausea; 0 energy; not feeling well; Fever 99.5 / Constant fever over 102 up to 104.3 / 99.3 fever; This is a spontaneous report from a contactable consumer (patient). A 52-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Lot number: EP6955, Expiration date was not reported), via an unspecified route of administration (administered on the right arm) on 28Mar2021 at 15:00 (at the age of 52-years-old) as dose 2, single for COVID-19 immunisation. Medical history included high blood pressure, seasonal migraine and known allergies to penicillin all from an unknown date. The patient didn't receive any other vaccines within 4 weeks prior to COVID vaccine. Prior to vaccination, the patient has not been diagnosed with COVID-19. Concomitant medications included cyanocobalamin (VITAMIN B 12), colecalciferol (VITAMIN D), ascorbic acid (VITAMIN C), bupropion, carvedilol, and estradiol all taken for an unspecified indication, start and stop date were not reported. The patient was previously vaccinated with the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19, Solution for injection; Lot number: EN6205, Expiration date was not reported), via an unspecified route of administration (administered on the right arm) on 07Mar2021 at 15:00 (at the age of 52-years-old) for COVID-19 immunisation. The patient experienced not feeling well and fever 99.5/constant fever over 102 up to 104.3/99.3 fever both on 29Mar2021 at 12:00 AM and severe aches all over, migraine headache, chills, nausea, and 0 energy all on 30Mar2021. It was further reported that within 8 hrs the patient was not feeling well, with in 10 hrs the patient had fever 99.5 and next two days constant fever over 102 up to 104.3, severe aches all over, migraine headache, chills, nausea, 0 energy. On the 3rd day, the patient had 99.3 fever but able to function and on the 4th day the patient was fine. No treatment was received for the events. The outcome of the events was reported as recovered on 01Apr2021 with lasting effects/sequel. No follow-up attempts are possible. No further information is expected.

Other Meds: BUPROPION; CARVEDILOL; ESTRADIOL; VITAMIN B 12 [CYANOCOBALAMIN]; VITAMIN D [COLECALCIFEROL]; VITAMIN C [ASCORBIC ACID]

Current Illness:

ID: 1792574
Sex: F
Age:
State: OH

Vax Date: 03/28/2021
Onset Date: 03/29/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Injection site pain; has knot with swelling; has knot with redness; Chills; Joint pain; Tiredness; Headache; This is a spontaneous report from a contactable consumer. An 85-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration, administered in the right arm on 28Mar2021 at 04:00 (at the age of 85 years old) (Lot Number: ER8730) as dose 1, single for COVID-19 immunisation. Medical history included ongoing high blood pressure, chronic pain from 1964 and ongoing, ongoing restless legs, and ongoing pain management. Concomitant medications included aspirin [acetylsalicylic acid] taken for an unspecified indication from an unspecified start date and ongoing; morphine taken for pain management from an unspecified start date and ongoing; valsartan taken for an unspecified indication from an unspecified start date and ongoing; trazodone taken for restless legs syndrome from an unspecified start date and ongoing. The patient had no prior vaccination (within 4 weeks). On 29Mar2021 at 10:00, the patient experienced injection site pain has knot with swelling and redness. On 29Mar2021 at 05:00, the patient experienced tiredness and headache. On 29Mar2021 at 06:00, the patient experienced chills and joint pain. The outcome of the events vaccination site pain, vaccination site swelling, and vaccination site erythema was recovering whereas outcome of the events fatigue, headache, chills, and arthralgia was recovered on 30Mar2021. No follow-up attempts are possible. No further information is expected.

Other Meds: ASPIRIN [ACETYLSALICYLIC ACID]; MORPHINE; VALSARTAN; TRAZODONE

Current Illness: Blood pressure high; Chronic pain; Pain management; Restless legs

ID: 1792575
Sex: F
Age:
State: FL

Vax Date: 03/29/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: Vaccination site erythema, Vaccination site pruritus, Vaccination site swelling

Symptoms: Chills; Fever; Felt like crap; Body aches; Eyes hurt when she moves them; Pains in her back; This is a spontaneous report from a contactable consumer. A 56-year-old female patient received first dose bnt162b2 (Solution for injection, Batch/Lot Number: ER2613; Expiration Date: Jul2021), dose 1 via an unspecified route of administration, administered in Arm Right on 29Mar2021 16:00 (at the age of 56 years) as dose 1, single for COVID-19 immunization. Medical history included exposure to sars-cov-2 from 27Mar2021 to an unknown date she was also exposed to her niece and grandchildren last Saturday who are COVID-19 positive, covid-19 from an unknown date and unknown if ongoing Her niece and grandchildren last Saturday who are COVID-19 positive. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 30Mar2021 the patient experienced chills, fever. on 29Mar2021 body aches, eyes hurt when she moves them. on 30Mar2021 felt like crap, pains in her back on Mar2021.The outcome of the events was chills, fever, felt like crap recovered. Body aches recovering, Eyes hurt when she moves them not recovered, Pains in her back was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1792576
Sex: F
Age:
State: NJ

Vax Date: 03/25/2021
Onset Date:
Rec V Date: 10/16/2021
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: I have a black and blue mark on my left arm; It's red and blue and its all over the front of my arm; This is a spontaneous report from a contactable consumer. This 91-year-old female consumer reported for herself A 91-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/lot number: ER8727 and expiration date: not reported) via an unspecified route of administration in left arm on 25Mar2021 (at the age of 91-years-old) as dose 1, single for covid-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date on 2021, the patient experienced i have a black and blue mark on my left arm, it's red and blue and its all over the front of my arm. It was reported that her shoulder down to elbow like five inches, have a black and blue mark on my left arm. The patient stated that she had the vaccination Thursday and I had Pfizer vaccination and now where she injected me from my shoulder down to my elbow like five inches. I have a black and blue mark on my left arm. And it is all around its look like that I had a 'short lead". It doesn't hurt. It is big mark it's like five inches down that's how big it is it looks like I have something on my arm. The outcome of all events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792577
Sex: F
Age:
State: AZ

Vax Date: 03/14/2021
Onset Date: 03/15/2021
Rec V Date: 10/16/2021
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: Blood pressure decreased, Chest pain, Chills, Confusional state, Decreased appetite

Symptoms: Swelling of throat and neck; Swelling of throat and neck; rash; hives; itching; This is a spontaneous report from a contactable consumer (patient). A 69-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EN6202, Expiration Date was not reported), via an unspecified route of administration, administered in the left arm on 14Mar2021 11:00 (at the age of 69-years-old), as dose 1, single for COVID-19 immunisation. The patient's medical history was not reported. Concomitant medications included atorvastatin; lisinopril; amlodipine; levothyroxine, all taken for an unspecified indication, start and stop date were not reported. The patient was not pregnant at the time of vaccination. Patient has no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19; and since the vaccination, has not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced swelling of throat and neck, rash, hives, itching on 15Mar2021 18:00. Events resulted to treatment with course of prednisone and hydroxyzine and Doctor or other healthcare professional office/clinic visit. The outcome of events was not reported. No follow-up attempts are possible. No further information is expected.

Other Meds: ATORVASTATIN; LISINOPRIL; AMLODIPINE; LEVOTHYROXINE

Current Illness:

ID: 1792578
Sex: F
Age:
State: PA

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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: some chills; fever; nausea; her right knee went out; she developed an ingrown toenail that was painful and she would not walk.; cough; ear hurting; stuffy nose; sore throat; just feeling sick; This is a spontaneous report from a contactable consumer (patient) received via Medical Information Team. A 76-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as dose 1, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On unspecified dates, after the first injection of the vaccine, the patient experienced some chills, fever, and nausea that went away. Later, she reports her right knee went out and she developed an ingrown toenail that was painful and she would not walk. She was able to get the ingrown toenail removed by a doctor and was prescribed cefalexin (CEPHALEXIN), taken 4 times a day. At the time of the report, the consumer was experiencing cough, ear hurting, stuffy nose, fever, chills, sore throat, and just feeling sick. The patient was uncertain if this was due to the vaccine, the cefalexin, or some other reason. The patient was scheduled to get the second dose. The patient recovered from nausea and ingrown toenail on unspecified dates while the outcome of the other events were unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792579
Sex: F
Age:
State: NV

Vax Date: 03/08/2021
Onset Date:
Rec V Date: 10/16/2021
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: Heart rate decreased, Heart rate increased, Hypertension, Injection site pain, Musculoskeletal chest pain

Symptoms: she was unable to get an appointment for the 2nd shot due on 29Mar2021; dizziness; fever; This is a spontaneous report from a Pfizer Sponsored Program. A contactable female consumer(patient) reported for herself that: A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number and Expiry date was not reported), via an unspecified route of administration on 08Mar2021 as DOSE 1, SINGLE for COVID-19 immunization. The patient medical history and concomitant medications was not reported. On an unspecified date, the patient experienced she was unable to get an appointment for the 2nd shot due on 29Mar2021 and patient experienced dizziness and fever that might have missed her 2nd shot. The outcome of the events was reported as unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792580
Sex: M
Age:
State: TX

Vax Date: 03/19/2021
Onset Date: 03/20/2021
Rec V Date: 10/16/2021
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: sinus drainage has significantly increased; dealing with joint pain; coughing more phlegm; This is follow-up spontaneous report from a contactable consumer (patient himself). A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 19Mar2021 as dose 1, single for COVID-19 immunisation. The patient medical history includes had a severe case of COVID on an unspecified date in July2020 and was hospitalized. The patient concomitant medications were not reported. It was stated that, he had the usual effects the next day that lasted for a day in a half. On 20Mar2021, the patient experienced sinus drainage has significantly increased, coughing more phlegm, and dealing with joint pain it has almost been two weeks since the first dose. He did not had his second dose and figured he would ask the manufacture of the study. The outcome of the events was unknown. No follow-up attempts are possible, information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1792581
Sex: F
Age:
State:

Vax Date: 03/31/2021
Onset Date:
Rec V Date: 10/16/2021
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: Arm hurts; Chills; This is a spontaneous report from a non-contactable consumer, the patient. An 18-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 31Mar2021 at 13:30 (at the age of 18-years-old) as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. Prior to the vaccination, the patient was diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On an unknown date in 2021 the patient experienced arm hurts and chills. 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 outcomes of the events arm hurts and chills were unknown at the time of report. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792582
Sex: F
Age:
State: IN

Vax Date: 03/27/2021
Onset Date:
Rec V Date: 10/16/2021
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: Sleepiness; Headache; Joint pain; Injection pain; High fever; Chills; This is a spontaneous report from a contactable nurse. A 57-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE ; Lot Number: ER8732; Expiration Date: 30Jun2021), via an unspecified route of administration on 27Mar2021 (at the age of 57-years-old) at dose 1, single for covid-19 immunization. The patient medical history were not reported. Patient take a number of medications. The patient experienced sleepiness, headache, joint pain, injection pain, high fever, chills on an unspecified date. Patient has been taking Tylenol and that helping for the events. The outcome of the events was unknown. The relationship between the vaccine and events was related. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792583
Sex: F
Age:
State: NY

Vax Date: 03/24/2021
Onset Date: 03/25/2021
Rec V Date: 10/16/2021
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: developed muscle and joint pains; developed muscle and joint pains; felt sore; sore on her arm; Tiredness; This is a spontaneous report from a contactable consumer or other non hcp (Patient). A 45-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration on 24Mar2021, Tuesday (at the age of 45-Years-old) (Batch/Lot number was not reported) as DOSE1, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On 25Mar2021, the patient experienced tiredness. she was tired a little the day after vaccination. She had tiredness on the 26Mar2021. That was fine by the 27Mar2021. On 26Mar2021, 2 days after vaccination, she experienced felt sore and had sore on her arm. She clarified the pain in her legs started on 30Mar2021 and not on 29Mar2021. On 30Mar2021, she developed muscle and joint pains. It was on and off. It was not unbearable, it was bearable. It may be a little bit better, it has moved from legs to kind of like just her quads or her thighs. It was reported that ever since she started having muscle and joint pain in her legs and she was researching that and it seems like it was a common thing but she was concerned that it happened like 7 days later she was wondering if there was any information on that or if she was in the right place to ask about that. It was reported that she had just finished her period which she knows was a little bit gross but that just finished right before this, she does not know if that had anything to do with it, it does not seem that way though. At the time of this report, the outcome of event felt sore and sore on her arm was unknown, developed muscle and joint pains was recovering and tiredness recovered on 27Mar2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792584
Sex: F
Age:
State: FL

Vax Date: 03/29/2021
Onset Date: 03/29/2021
Rec V Date: 10/16/2021
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: creatinine; Result Unstructured Data: Test Result:high creatinine level; Test Date: 20210331; Test Name: Fever; Result Unstructured Data: Test Result:102?F; Test Date: 20210331; Test Name: Fever; Result Unstructured Data: Test Result:it was low grade like around 100; Test Date: 20210331; Test Name: oxygen level; Result Unstructured Data: Test Result:90, when I was sitting down; Comments: when I am sitting down relaxed and I never had it that low

Allergies:

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

Symptoms: redness in her injection arm; body aches; chills; fever; oxygen level, it gets roll into 90, when I was sitting down; sore arm; headache; Gets worsened; This is a spontaneous report from a contactable consumer (patient). A 52-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number was not reported), via an unspecified route of administration, administered in left arm on 29Mar2021 as dose 1, single (at the age of 52-years-old) for COVID-19 immunization. Medical history included hypertension, high cholesterol, asthma, helps me breath, and high creatinine. It was reported that, the patient when probed about medical history stated, she was about to undergo some testing for Kidney, a physician found high creatinine level and so he got to go tested. Concomitant medications included metoprolol and hydrochlorothiazide, lisinopril; both taken for hypertension, Astra Statin and fenofibrate; both taken for high cholesterol, salbutamol sulfate (PROAIR HFA) taken for asthma, alprazolam taken for helps me breath; all start and stop dates were not reported. On 29Mar2021, the patient had a sore arm and little bit of headache for the first 2 days and then the patient started getting body aches, and it started getting worse. On 31Mar2021, the patient started to experience redness in her injection arm, body aches and chills and has a fever of 102 (degree) F. The patient on 31Mar2021, has experienced oxygen level on oximeter, it gets roll into 90, when she was sitting down. The patient had an increasingly bad reaction, had body chill and aches and It was reported that overnight it turned into fever and, it was low grade like around 100 and in past couple of hours it has gone up. The patient had taken Tylenol 1000mg. Upon reconfirmation patient stated, her oxygen level went down to 90, when she was sitting down relaxed, and never had it that low. The patient confirmed that all the events the patient was experiencing was since 31Mar2021. The patient also stated it gets worsened when asked whether still experiencing the problem. The patient confirmed taking Tylenol 1000mg about an hour, may be quite an hour bit. The patient underwent lab tests and procedures which included blood creatinine: high creatinine level on an unspecified date, body temperature: 102-degree F on 31Mar2021, body temperature: it was low grade like around 100 on 31Mar2021, oxygen saturation: 90, when she was sitting down relaxed, and never had it that low on 31Mar2021. Therapeutic measures were taken as a result of body aches, chills, fever, sore arm, and headache. The patient had recovered from the events headache and sore arm on 31Mar2021. The patient had not recovered from the other events at the time of report. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: ALPRAZOLAM; METOPROLOL; LISINOPRIL AND HYDROCHLOROTHIAZIDE; FENOFIBRATE; PROAIR HFA

Current Illness:

ID: 1792585
Sex: F
Age:
State: CO

Vax Date: 04/01/2021
Onset Date: 04/01/2021
Rec V Date: 10/16/2021
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:

Allergies:

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

Symptoms: Pain in my left arm; This is a spontaneous report from a contactable consumer, the patient. A 45-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 left arm on 01Apr2021 at 14:00 (at the age of 45-years-old) as a single dose for COVID-19 immunisation. The patient had no medical history. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient had no known allergies to medications, food or other products. The patient received unspecified medication within two weeks of vaccination. The 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 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 vaccination. On 01Apr2021 at 15:00, the patient experienced pain in her left arm. The event did not result in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. The patient did not receive any treatment for the reported event. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event pain in her left arm was recovered on 01Apr2021. No follow-up attempts are required; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792586
Sex: F
Age:
State: WI

Vax Date: 03/24/2021
Onset Date: 03/24/2021
Rec V Date: 10/16/2021
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: Unevaluable event

Symptoms: she has a small rash on her leg; feeling unwell; slight fever; swollen lymph nodes; terrible headache; so much tiredness / fatigue; chills; joint pain all over; muscle stiffness; been sleeping a lot; dizziness; weakness; flu like symptoms; pain at injection site; feeling warm; nauseous; This is a spontaneous report received from a contactable consumer (patient) via Pfizer sponsored program COVAX US Support. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on 24Mar2021 as dose 1, single for covid-19 immunization. Patient medical history included depression and under medications (unspecified), migraine, autoimmune disorder and has compromised issues from an unknown date and unknown if ongoing. Patient had allergies [unspecified]. Concomitant medication included unspecified medication of depression. On 24Mar2021, the night after receiving the first shot of vaccine patient experienced flu like symptoms, pain at injection site, feeling warm, nauseous. Patient reported that 24 hours later on 25Mar2021, patient was feeling unwell, slight fever, has swollen lymph nodes, terrible headache, so much tiredness/fatigue, chills, joint pain all over, muscle stiffness, been sleeping a lot, dizziness, weakness for 3 days. Patient stated she has a small rash on her leg and doesn't know where it came from on an unspecified date. Patient wanted to know if that was okay for her to take Midol asking if that was a safe thing to be done after receiving the 1st dose and was concerned with the side effects and what she needs to be done prior to taking the 2nd dose. Outcome of the events flu like symptoms, pain at injection site, feeling warm, nauseous and rash on leg were unknown and the rest of the events was recovered on 28Mar2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792587
Sex: M
Age:
State: TN

Vax Date: 03/01/2021
Onset Date: 03/07/2021
Rec V Date: 10/16/2021
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: Chills, Dizziness, Injection site pain, Myalgia, Pyrexia

Symptoms: Having dizzy spells and headache and pain in the injection area; Having dizzy spells and headache and pain in the injection area; Having dizzy spells and headache and pain in the injection area; This is a spontaneous report from a contactable consumer. A 44-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 an unknown date in Mar2021 at 13:15 (at the age of 44-years-old) as a single dose for COVID-19 immunisation. Medical history included diabetes, hypertension, schizoaffective disorder and narcolepsy. The patient had no known allergies to medications, food, or other products. Concomitant medications taken within two weeks of vaccination included metformin (MANUFACTURER UNKNOWN), glipizide (MANUFACTURER UNKNOWN), oxybate sodium (XYREM), armodafinil (MANUFACTURER UNKNOWN), hydrochlorothiazide, lisinopril (LISINOPRIL HCTZ), simvastatin (MANUFACTURER UNKNOWN), risperidone (MANUFACTURER UNKNOWN), agrimonia eupatoria (AGRIMONY), guaifenesin (MUCINEX), cetirizine (MANUFACTURER UNKNOWN), chondroitin sulfate, glucosamine hydrochloride (OSTEO BI-FLEX), boron, chromium, copper, germanium, iodine, manganese, molybdenum, selenium, silicon, sitosterol, vanadium, vitamin d nos, zinc (SUPER BETA PROSTATE), probiotics and curcuma longa rhizome (TURMERIC); all for unknown indication from unknown date and unknown if ongoing. 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 07Mar2021 at 14:00, the patient was having dizzy spells and headache and pain in the injection area. 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, emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event having dizzy spells and headache and pain in the injection area was resolved with sequelae 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: METFORMIN; GLIPIZIDE; XYREM; ARMODAFINIL; LISINOPRIL HCTZ; SIMVASTATIN; RISPERIDONE; AGRIMONY; MUCINEX; CETIRIZINE; OSTEO BI-FLEX [CHONDROITIN SULFATE;GLUCOSAMINE HYDROCHLORIDE]; SUPER BETA PROSTATE; TURMERIC [CURCUMA LONGA RHIZOME]

Current Illness:

ID: 1792588
Sex: F
Age:
State: OH

Vax Date: 03/19/2021
Onset Date: 03/26/2021
Rec V Date: 10/16/2021
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: burning feeling at location of injection started about 1 week after injection. Feels similar to initial injection. Not swollen or red.; This is a spontaneous report from a contactable consumer, the patient. A 52-year-old non-pregnant female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6202) via an unspecified route of administration in the arm left on 19Mar2021 at 13:45 (at the age of 52-year-old) as a single dose for COVID-19 immunisation. Medical history included high blood pressure (HBP). Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not have any allergies to food, medications, or other products. Concomitant medications included lisinopril (MANUFACTURER UNKNOWN), metoprolol (METROPROLOL) and colecalciferol (VITAMIN D3) for an unknown indication from an unknown date and unknown if ongoing. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 26Mar2021, the patient experienced burning feeling at location of injection started about 1 week after injection and it was not swollen or red. The patient felt similar to initial injection. The events 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. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event burning feeling at location of injection was not resolved at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds: LISINOPRIL; METOPROLOL; VITAMIN D3

Current Illness:

ID: 1792589
Sex: U
Age:
State:

Vax Date: 03/26/2021
Onset Date: 03/28/2021
Rec V Date: 10/16/2021
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: Shot site, it's kind of puffed up; Rash from my shoulder to midway my arm after the shot; This is a spontaneous report from a contactable consumer (patient). A patient of an unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EN6205, Expiration date: Not reported), via an unspecified route of administration on 26Mar2021 as dose 2, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number and expiration date were not reported), via an unspecified route of administration on 25Feb2021 as dose 1, single for COVID-19 immunization. After the second vaccination, the patient's shot site was kind of puffed up and rash from the shoulder to midway of the arm after the shot on 28Mar2021. It was reported that the patient took some diphenhydramine (BENADRYL) and wanted to know what should be taken for these events. The patient also wanted to know why they need all the event related information and informed that what need to be done from the patient's end. The outcome of the events was unknown at the time of report. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792590
Sex: F
Age:
State:

Vax Date: 03/26/2021
Onset Date:
Rec V Date: 10/16/2021
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: This is a spontaneous report from a noncontactable consumer (patient). A female patient, of an unspecified age, received the 1st dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, solution for injection, batch/lot# not reported), via an unspecified route of administration, on Mar 26, 2021, single dose, for COVID-19 immunisation. The patient's medical history and concomitant medications not reported. On an unspecified date, patient had a rash at the injection site and described it as "itching real bad" and "very painful." The outcome of the event: unknown. No follow-up attempts possible. Information about lot/batch number cannot be obtained. No further information expected.

Other Meds:

Current Illness:

ID: 1792591
Sex: F
Age:
State:

Vax Date: 03/31/2021
Onset Date: 04/01/2021
Rec V Date: 10/16/2021
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: woke up with a very red face that has been red for 5 hours or so; This is a spontaneous report from a contactable consumer (patient). A 22-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported, Expiry date: unknown), dose 1 via an unspecified route of administration on 31Mar2021 (at the age of 22 years) as dose 1, single for covid-19 immunisation. The medical history and concomitant medications were not reported. The patient woke up with a very red face that has been red for 5 hours or so on 01Apr2021 and it had not gone down. Her face never got red at all ever. She wanted to know if that was normal or should she be concerned. The outcome of the event was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1792592
Sex: F
Age:
State:

Vax Date: 03/13/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: joint pain in her ankles, knuckles and back; joint pain in her ankles, knuckles and back; Joint pain; Aches/Body ache; Fever/Low grade fever; Dehydration; Indigestion/Heartburn; Fatigue/tired; Lip was twitching briefly; Sleeplessness; Nauseous; This is a spontaneous report from a contactable consumer (patient). A 24-years-old female patient received BNT162b2 (Pfizer BioNTech Covid-19 mRNA Vaccine, Solution for injection; Batch/Lot number: EN6208, Expiry date, NDC number, UPC number was not reported), via an unspecified route of administration on 13Mar2021 as dose 1, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On Mar2021, patient experienced joint pain, aches/body ache, fever/low grade fever, dehydration, indigestion like heartburn, and fatigue/pretty tired for a week, sleeplessness, nauseous after receiving her vaccine dose. On Mar2021, patient lip was twitching briefly after receiving the vaccine dose, Patient stated that most of her symptoms went away 1 week after receiving the dose. On 28Mar2021, patient stated that her joint pain returned and describes it as mild and sporadic joint pain in her ankles, knuckles and back, like patient have not had to take any medicine or anything for it but patient do notice that she had some joint pain (was fine and then this past Sunday patient started feeling like joint pain). Patient was supposed to get her second dose of the vaccine 03Apr2021. Patient wanted to know if these side effects had been reported and wanted to know if Pfizer had data on individuals who had severe allergic reactions and did, they had them mostly after the first or the second dose. The outcome of joint pain in her ankles, knuckles and back was not recovered and recovered for rest of the events on Mar2021.

Other Meds:

Current Illness:

ID: 1792593
Sex: M
Age:
State:

Vax Date: 03/31/2021
Onset Date:
Rec V Date: 10/16/2021
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: headaches; flu like symptoms; joint soreness; This is a spontaneous report from a contactable consumer (patient). A 38-year-old male patient received second dose of bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 31Mar2021 as dose 2, single for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. Patient previously took first dose of BNT162B2 (Pfizer-BioNTech COVID-19 Vaccine) on an unspecified date (at the age of 38-year-old) for covid-19 immunisation. On an unspecified date in 2021, the patient experienced headaches, flu like symptoms and joint soreness. They also wanted to know if it was okay to take tylenol or ibuprofen or will it interfere with antibody production. The event was reported a non serious. The outcome of all the events was unknown. No follow-up attempts are possible; information about lot batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021366793 same reporter/drug/AE with different patient

Other Meds:

Current Illness:

ID: 1792594
Sex: M
Age:
State: MI

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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: few aches and pains; joint pain; muscle pain; headaches; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age (reported as age: 51; unit: unknown) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Batch/lot number and expiration date were not reported), via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunisation. Medical history included asthma from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient experienced some symptoms, such as a few aches and pains on an unspecified date. The patient mentioned "joint pain, muscle pain and headaches" on an unspecified date. The outcome of the events was unknown. The patient was querying on how soon after the shot can he take other medications, such as Advil and Advair. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792595
Sex: F
Age:
State: NY

Vax Date: 03/23/2021
Onset Date: 03/24/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Name: bloodwork; Result Unstructured Data: Test Result:everything was perfect; Test Name: temperature; Result Unstructured Data: Test Result:99.7; Comments: (units unspecified); Test Name: EKG; Result Unstructured Data: Test Result:everything was perfect; Test Date: 20210324; Test Name: Shortness of breath; Result Unstructured Data: Test Result:1.5; Test Name: sonogram; Result Unstructured Data: Test Result:everything was perfect

Allergies:

Symptom List: Injection site pain

Symptoms: difficulty of breathing/shortness of breath; chest tightness/Chest heaviness; arm hurt; Wheezing; pain in her chest; the highest her temperature got was 99.7; This is a spontaneous report from a contactable consumer (patient) via Medical Information Team. A 41-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EN6207), dose 1 via an unspecified route of administration, administered in Arm Left on 23Mar2021 at 17:30 (24-hour clock) (Age at Time of Vaccination: 41 years-old) as DOSE 1, SINGLE for COVID-19 immunisation. No medical history and no concomitant medications were reported. Patient had no allergies. The patient had no Family Medical History Relevant to adverse events. Patient had no history of all previous immunization with the Pfizer vaccine considered as suspect, Vaccination Facility Type was other and was not administered at Military Facility. No additional vaccines were administered on same date of the Pfizer Suspect. The patient took no Prior Vaccinations (within 4 weeks). The patient experienced difficulty of breathing/shortness of breath, chest tightness/chest heaviness, arm hurt, wheezing on 24Mar2021 at 18:00 and pain in her chest, the highest her temperature got was 99.7 was on an unspecified date in 2021. Patient stated that she worked Wednesday, Thursday and Friday were just fine, had no type of symptoms the first night, but the second night she had tad of wheezing, only a minute worth, and a little tightness in her chest and shortness of breath on a scale of 1.5/10 but it was to the point she called her doctor. States her doctor said she didn't want to see her and that was normal. States she is calling to see if that is normal and because she has concerns about receiving the second dose, since she had this reaction with the first dose. Clarified her wheezing was only for one minute. Stated her husband said oh great, she was fine until she got the vaccine, she called an allergist and they said they only give Moderna, so they have no idea about the Pfizer vaccine, called the urgent care but they are not giving out vaccines so they did not know and so she figured she would call here to see what type of information she can find out. And now she was still having a little bit of tightness in her chest and shortness of breath, was concerned, but not frightened, just concerned about the second one because she has heard it can be difficult and she loves life and wants it to continue. She was nervous because everyone says the second dose is tougher. Clarified that it did not stop her activities, she still went to work, the highest her temperature got was 99.7, and her arm hurt for a couple of days, has no allergic reactions to anything. She just wanted to check before she takes the next one, she does not want to dump it all on nurse the day of her vaccine, wanted to be proactive rather than reactive. She stated no one knows where she lives. States she knows Pfizer gives no medical advice, but she wanted to know what next step is, maybe its fine. She went and walked for 1.5hours and did okay but feels a little bit of heaviness in her chest that she has never felt before, Stated if this were a one and done type of shot she would figure it will go away, but it was just before her second one and she has a young child, so she was concerned, Stated everyone was so scared where she lives because the numbers are going up and the doctor offices do not want people coming in. States people tell her about the second one, that it brought them down and if she had shortness of breath with the first one and still feels it a bit, she wanted to reach out and she was finding no answers anywhere. States she wants to get the vaccine and be done, but she also wants to be safe. She was on no medication of any kind other than vitamins and she has no health issues and everything was perfect at her last appointment. Patient had her first dose 23Mar the following day she had a very slight shortness of breath for 4 nights, wheezing for a minute and pain in her chest. It was weird because her father and uncle had nothing, and they both took the Pfizer. Adverse Event Time of Onset (24-hour clock) was evening 18:00. The patient had no adverse events following prior vaccinations. The patient underwent lab tests and procedures which included blood test: everything was perfect on an unspecified date, body temperature: 99.7 on (units unspecified) an unspecified date, electrocardiogram: everything was perfect on an unspecified date, laboratory test: 1.5 on 24Mar2021 and ultrasound scan: everything was perfect on an unspecified date. Patient not visited to emergency room or physician's office for the events. No therapeutic measures were taken as a result of the events. The outcome of the events difficulty of breathing/shortness of breath and chest tightness/Chest heaviness was not recovered, arm hurt recovered on 26Mar2021, Wheezing recovered on 24Mar2021 and pain in her chest, the highest her temperature got was 99.7 was unknown. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792596
Sex: F
Age:
State: WA

Vax Date: 03/14/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: cold; sick; cough; This is a spontaneous report from a contactable consumer (patient) reported for herself. A female patient of an unspecified age received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route on 14Mar2021, as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The second dose was scheduled on 03Apr2021. The patient had cold on 29Mar2021, sick and cough on an unspecified date in Mar2021. The clinical course includes when she went to have her first covid vaccine there was a paper that asked if you are allergic to anything. Her sister said it said or are you sick. Caller states she has been sick for about 3 days and asks if it is safe to get the vaccine with a cold. She was going for her second vaccine on Saturday. Caller states the paper said have you done steroids in the last week or something like that but that can't remember what it said. Clarified with caller details and states that both her and her sister saw the paper and she thought she signed it. Caller states it was just a cold, she gets a cold about once a year. The patient took cough medicine and Alka-Seltzer Plus once. Caller also asked if it's okay to proceed with her 2nd dose of the vaccine even if she has colds. The outcome of events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792597
Sex: M
Age:
State: OH

Vax Date: 01/28/2021
Onset Date:
Rec V Date: 10/16/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: itching all over his body; stomach felt upset; can't walk around; This is a spontaneous report from a Regulatory Authority. contactable consumer. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, formulation: solution for injection) via an unspecified route of administration on 28Jan2021 as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced itching all over his body after 10 days and advised to take Benadryl and until 2nd shot (18Feb2021). The patient was still taking Benadryl and when his stomach felt upset, bad and can't walk around and even can't sit so decided to stop taking that medicine but the itching didn't stop. The patient mentioned after he stopped taking the Benadryl his arms, behind ears, shoulder and his back was itching and it doesn't stay on one spot. Therapeutic measures were taken as a result of itching all over his body. The outcome of the event itching all over his body was not recovered. The outcome of the events stomach felt upset and can't walk around was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792598
Sex: F
Age:
State: NC

Vax Date: 03/31/2021
Onset Date:
Rec V Date: 10/16/2021
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: Have a small bump at the injection site; The area is pink and itches/she felt a knot there that is red and pink, she wants to itch at it, she thinks it might just be because of the person that gave her the dose; Sore arm; Small pink spot and got bigger and bigger with a large knot; it is about 4 in by 4 in; This is a spontaneous report from a contactable consumer (patient). A 55-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot Number: not reported, Expiry date: not reported) via an unspecified route of administration, administered in Arm Left on 31Mar2021 (at the age of 55 years old) as dose 2, single for COVID-19 immunization. Medical history included: hypertension She has had this condition for 3 or 4 years and received lisinopril hctz for hypertension at the dose of 20mg/25mg once a day. Concomitant medication(s) included celecoxib (CELEBREX) taken for arthritis. The patient previously BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Lot Number: EN6208, Expiry date: 30Jun2021) via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization and experienced pain in extremity. Got her second shot on 31Mar2021 and the first one, she initially said two weeks before and then after being told it was to be given 3 weeks apart, she said yes, it was probably 3 weeks. She has reported this to us before but just wanted to confirm that this was a side effect. She knows some people who got the Moderna shot and had worse side effects. The reporter was calling about the Pfizer COVID 19 shot. She says she got the 2nd shot yesterday (31Mar2021) and, she doesn't consider it a side effect, she had no problems except a sore arm which she had from the first one too. However, this afternoon she felt a knot there at the injection site that is red and pink. She wants to itch at it. She thinks it might just be because of the person that gave her the dose. She says she doesn't really think it is an event, she knows any time you get shots you can get a knot. She just wants to make sure it doesn't mess with getting all the vaccine she is supposed to get. She wants to talk to someone about that. She says she has no headache, no fever, nothing like that. Caller declines to fill out a report, she says she would rather just talk with a nurse or whatever to ask her question. The patient Had a reaction to her Pfizer covid 19 shot. She looked on the CDC website and they had it listed as Covid arm. After the first shot, it was just sore but after the second shot, it started out as a small pink spot and got bigger and bigger with a large knot; it is about 4 in by 4 inches, she had a knot. Over the weekend, it got bigger and was 3-4 inches by 3-4 inches. The patient did not receive any treatment for the events. The outcome of the events was unknown. Follow up attempts are completed. No further information was expected.

Other Meds: CELEBREX

Current Illness:

ID: 1792600
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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: rash; tired; sore; dont want to wake; flu like symptoms; This is a spontaneous report from a contactable consumer (patient). A 45-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number and expiry date not reported), via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced rash all up the right side of leg, very tired, sore, didn't want to wake up and flu like symptoms on an unspecified date. The outcome of the events was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792601
Sex: F
Age:
State: TX

Vax Date: 03/31/2021
Onset Date: 03/31/2021
Rec V Date: 10/16/2021
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: Test Name: temperature; Result Unstructured Data: Test Result:99.3 Fahrenheit

Allergies:

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

Symptoms: feels unwell; has a temperature of 99.4 F/fever; injection site pain; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 66-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection, Lot Number: EP7533), dose 2 via an unspecified route of administration, administered in arm left on 31Mar2021 at 12:46 as DOSE 2, SINGLE (at the age of 66-years-old) for covid-19 immunisation. The patient medical history was not reported. The patient had no history of drinking, smoking or doing drugs. No prior vaccinations (within 4 weeks). The patient concomitant medications included ongoing aspirin (ASPIRIN [ACETYLSALICYLIC ACID]) (81 mg once daily) taken for an unspecified indication, start and stop date were not reported. The patient previously took sulfamethoxazole and experienced drug hypersensitivity presented as an all over body rash that started on the 10th day of a 10 day regimen, prednisone and experienced drug hypersensitivity, ampicillin and experienced drug hypersensitivity on day 3 of a 10 day regimen and compazine [prochlorperazine maleate] for nausea and experienced drug hypersensitivity. Historical vaccine included first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection, Lot Number: unknown), dose 1 via an unspecified route of administration, administered in arm left on 10Mar2021 at 12:46 as DOSE 1, SINGLE (at the age of 66-years-old) for covid-19 immunisation. The patient experienced injection site pain on 31Mar2021, feels unwell on an unspecified date. The patient had a temperature of 99.4 f on 01Apr2021. She knew her temperature every hour of every day. Since the Covid 19 virus started she had taken her temperature a lot. She had already on her second digital thermometer. Her temperature today was 99.3F. She was asking when she can start to take tylenol for her fever. She did not want the fever to get worse, she wanted tonip it in the bud. She reported the fever began within 23 hours of receiving her second covid 19 vaccine. Adverse events did not require a visit to emergency room/ physician office. The patient underwent lab tests and procedures which included body temperature: 99.3 fahrenheit on an unspecified date. The clinical outcome of the event temperature of 99.4 f was not recovered and other events were unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: ASPIRIN [ACETYLSALICYLIC ACID]

Current Illness:

ID: 1792602
Sex: F
Age:
State: PA

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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: itching and tingling in her "lips, mouth, and skin"; itching and tingling in her "lips, mouth, and skin"; itching and tingling in her "lips, mouth, and skin"/itching on her arm /itching was on the caller's neck /spreading to her face and chin; itching and tingling in her "lips, mouth, and skin"; itching and tingling in her "lips, mouth, and skin"; itching and tingling in her "lips, mouth, and skin"; lips were itching and swelling; Had allergic reaction to the first dose; This is a spontaneous report from a contactable consumer from a Pfizer-sponsored program. A female patient of an unspecified age (Age: 60; Unit: Unknown as reported) received first dose bnt162b2 (Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. Medical history included asthma, diabetes, shellfish allergy. Concomitant medications included budesonide, formoterol fumarate (SYMBICORT) for asthma. The patient previously took Advair for asthma. On an unspecified date, the patient experienced itching and tingling in her "lips, mouth, and skin" and stated the next day these symptoms transferred to her face and her chin. She reported having no trouble breathing, no weakness, no fast heartbeat, no swelling in the face or throat, and no dizziness. She stated that she spoke with a pharmacist who recommended she take Benadryl so she did for a week, which was how long her symptoms lasted before going away. 10 mins after the vaccine the caller was itching on her arm. The next day the itching was on the caller's neck. And then the next day the caller's lips were itching and swelling, and it was spreading to her face and chin the next couple of days. The caller called her primary care about this but no one was there. The caller then called the pharmacist and the pharmacist told her to get some Benadryl which she took for over a week. Second immunization coming up. Had allergic reaction to the first dose. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: SYMBICORT

Current Illness:

ID: 1792603
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
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 Name: fever; Result Unstructured Data: Test Result:100.5-100.7 Fahrenheit

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: headache; fever of 100.5-100.7 F; aching at the injection site; This is a spontaneous report from a non-contactable consumer (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as dose 1, single for COVID-19 immunisation. Medical history included COVID-19 from Jan2020 to an unknown date. The patient's concomitant medications were not reported. On an unspecified date, the patient experienced headache, fever of 100.5-100.7 F, and aching at the injection site. It was reported by the patient that she was told to receive the 1st dose 3 months after recovering from the virus but she received it 2 months after. The patient wanted to know if she should receive the 2nd dose 3 or 4 weeks after her 1st dose instead so that it would be 3 months after she had COVID. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792604
Sex: M
Age:
State: CO

Vax Date: 03/24/2021
Onset Date: 03/25/2021
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 20210327; Test Name: Body temperature; Result Unstructured Data: Test Result:100.2; Comments: degree; Test Date: 20210329; Test Name: COVID-19 RT PCR; Test Result: Negative ; Test Date: 20210329; Test Name: Nasal Swab; Test Result: Negative

Allergies:

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

Symptoms: Weakness; 100.2 degree fever; body aches; chills; severe headache; sinus and chest congestion; sinus and chest congestion; nausea; dry heaves; loss of appetite/no appetite; loss of taste/not taste; loss of smell/no smell; sore throat; runny nose; This is a spontaneous report from a contactable consumer (patient). A 45-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration, administered in the right arm on 24Mar2021 at 18:45 (at the age of 45 years old) (Lot Number: EP6955) as dose 1, single for COVID-19 immunisation. Medical history included no (reported other medical history- No). The patient's concomitant medications were not reported. The patient has no known allergies. The patient did not receive other vaccine in four weeks. The patient did not receive other medications in two weeks. The patient did not have COVID-19 prior to vaccination. The patient had been tested for COVID post-vaccination. On 25Mar2021, the patient experienced sore throat and runny nose. On 26Mar2021, the patient experienced body aches, chills, severe headache, sinus and chest congestion, nausea, dry heaves, loss of appetite, loss of taste, and loss of smell. On 27Mar2021, the patient experienced 100.2 degree fever. On 28Mar2021, the patient experienced weakness. The course of the events was as follows: Day 1: sore throat, runny nose; Day 2: body aches, chills, severe headache, sinus and chest congestion, nausea, dry heaves, loss of appetite, loss of taste, loss of smell; Day 3: 100.2 degree fever, severe headache, sinus and chest congestion, body aches, chills, no appetite, not taste, no smell; Day 4: Weakness, minor headaches, minor sinus and chest congestion, cough, return of some appetite taste and smell. No treatment was received for the events. The patient underwent lab tests and procedures which included SARS-CoV-2 test (COVID-19 RT-PCR): negative on 29Mar2021 and SARS-CoV-2 test (Nasal Swab): negative on 29Mar2021. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1792605
Sex: F
Age:
State:

Vax Date: 03/19/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: pain in site, and in forearm, that also happened when vaccine was injected; pain in site, and in forearm, that also happened when vaccine was injected; chills; fever; congestion; achy; This is a spontaneous report from a non-contactable other health care professional (nurse). A female patient of a 68 (units unknown) age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number was not reported, Expiry date: not reported), dose 1 via an unspecified route of administration, administered at unspecified anatomical location on 19Mar2021 (age at vaccination was 68 (units unknown) as dose 1, single for COVID-19 immunization. Medical history included shortness of breath. The patient concomitant medications were not reported. In Mar2021, The patient experienced chills, fever, congestion. On 19Mar2021, patient also experienced pain in site, and in forearm, that also happened when vaccine was injected. on an unspecified date, experienced achy. The patient stated that she did not take any medications and suspected that she may have had covid 3 or 4 months before it hit her region, but no testing was done, so she never had a PCR test. The patient may be a little bit of long hauler with ongoing symptoms. The patient had shortness of breath with the virus but haven't taken pulse ox in a while. The patient major concern is because she had 18 hours of achy, chills, after the first dose, and thinking, this may be a little bit more information toward (or indicating) that she did have it last year. The patient plan was to wait two weeks and donate blood. to decrease her volume by 10 % and a week later when she has a chance to recoup get the second dose, hoping that it may lessen the response from the second dose. Long haulers from the virus have not found a good way to alleviate those symptoms, they try, vitamin C, NAC, heat, ice. A couple of issues to help with symptoms, but not working much. There are people who have had the virus that respond to the first dose and respond to the second dose with a spiking temp and getting symptoms again, and then it clears, and their energy comes back, they don't experience as much shortness of breath and there is a lifting of brain fog, they basically feel 80 % back to normal. The patient wanted to know whether she can donate blood, if she chooses to donate blood tomorrow she should have some antibodies, it's good for them they get a unit of blood and a unit of blood with antibodies. The patient was wondering if by donating blood would it lessen the effects of the second dose. The (institution name) says if you are 3 days away from the injection you are good to donate. The patient wanted to know whether she can be in clinical trial. Where she one of population in 1.5 million people, only 300,000 have registered for the vaccine. The outcome of chills, fever, congestion, vaccination site pain, pain was unknown and outcome of pain in extremity was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792607
Sex: M
Age:
State:

Vax Date: 03/11/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: First vaccine 18Feb2021, raised rash inner arms, arm pits, body sides, stomach inner thighs. After second dose moved to upper thighs and back; This is a spontaneous report from a contactable consumer. A 78-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection), dose 2 via an unspecified route of administration, administered in left arm on 11Mar2021 (Batch/Lot Number: En6199) as dose 2, single (at the age of 78 years old) for COVID-19 immunisation. Medical history included osteoporosis taking pravastatin, gabapentin, omeprazole. The patient's concomitant medications included pravastatin, gabapentin, omeprazole start and stop date not reported for unknown indication. The patient previously took first vaccine 18Feb2021 BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection) for COVID-19 immunisation and experienced raised rash inner arms, arm pits, body sides, stomach inner thighs. From first vaccine, raised rash inner arms, arm pits, body sides, stomach inner thighs and after second dose moved to upper thighs and back on Mar2021. Resulted in doctor or other healthcare professional office/clinic visit. Treatment was first a steroid shot, then on 29Mar2021, prednisone. The outcome of event was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: GABAPENTIN; PRAVASTATIN; OMEPRAZOLE

Current Illness:

ID: 1792608
Sex: M
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Name: Fever; Result Unstructured Data: Test Result:jumping from 100 to 104

Allergies:

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

Symptoms: extreme fatigue; fever/Fever is jumping from 100 to 104; Sick; This is a spontaneous report from a contactable consumer, the patient. A male patient of an unspecified age received first dose of bnt162b2 (PFIZER BIONTECH COVID 19 mRNA VACCINE, formulation: solution for injection, lot number was not reported), via an unspecified route of administration on an unspecified date as dose 1, single for covid-19 immunisation. Medical history included spleen removal 25 years ago. The patient's concomitant medications were not reported. The patient reported that he has a fever, and extreme fatigue on an unknown . The patient had the shot Tuesday morning, on an unknown, he meant hours kept me sick. Fever was jumping from 100 to 104 and asked for data regarding people like him that do not have a spleen and their experience with the Pfizer shot. The patient underwent lab tests which included body temperature jumping from 100 to 104 on an unknown date. The outcome of all the events was unknown. No follow-up attempts are possible. Information on Lot/Batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1792609
Sex: F
Age:
State: SC

Vax Date: 03/30/2021
Onset Date:
Rec V Date: 10/16/2021
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 Name: Fever; Result Unstructured Data: Test Result:101

Allergies:

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

Symptoms: rash on my face, all over my arm, on my back, on my stomach; fever; muscle pain; lymph nodes are swollen; Chills; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 20-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: ER8734, Expiration date: not reported) via an unspecified route of administration on 30Mar2021 (at the age of 20-years-old) as dose 1, single for covid-19 immunization. Medical history included birth control. Concomitant medication(s) included paracetamol (TYLENOL); diphenhydramine hydrochloride (BENADRYL); ethinylestradiol, norgestimate (TRI-SPRINTEC) taken for birth control, start and stop date unknown. On an unspecified date, patient experienced rash on my face, all over my arm, on my back, on my stomach, fever about 30 minutes ago, muscle pain, lymph nodes are swollen, chills. On an unspecified date, patient underwent lab tests and procedures which included body temperature was 101. Patient would like to know what she should do about side effects and if it is safe to get second dose of vaccine. The outcome of all events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: TYLENOL; BENADRYL; TRI-SPRINTEC

Current Illness:

ID: 1792610
Sex: F
Age:
State: ME

Vax Date: 03/25/2021
Onset Date: 03/26/2021
Rec V Date: 10/16/2021
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: strange taste in mouth / tasting sauteed green onions and green peppers; smelling and tasting sauteed green onions and green peppers; voice a little hoarse; chest hurts when taking a deep breath; This is a spontaneous report from a contactable consumer (patient). A 53-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, Lot number: EP6955), via an unspecified route of administration, administered on right arm (reported as right upper arm) on 25Mar2021 at 13:00 (age at vaccination was 53-year-old) as dose 1, single for COVID-19 immunization. The patient's medical history included ongoing optic neuritis (had for 7 years; in both eyes), ongoing thyroid problems (had probably 20 years or so), ongoing gastrointestinal problems, gall bladder issues, migraine and allergies. The patient's concomitant medications included ongoing fluoxetine 20 mg capsule, latanoprost eye drops, levothyroxine sodium 75 mg for thyroid, ongoing pantoprazole sodium 40 mg tablet, ongoing valproic acid 250 mg capsule for migraine and an over the counter medicine for allergies. The patient did not receive any other vaccine within 4 weeks prior to COVID-19 vaccine. On 26Mar2021, the patient experienced strange taste in mouth; smelling and tasting sauteed green onions and green peppers; voice a little hoarse and chest hurts when taking a deep breath. It was further reported that the strange taste in her mouth started day after the vaccine and slowly started to linger away or dwindle. The patient was smelling and tasting sauteed green onions and green peppers and it was out of the blue when it came but was slowly disappearing. It was reported that her voice has been a little hoarse and was still the same until the report. Her chest hurts when she takes a deep breath in sometimes, she describe it like the feeling you get when you are out in the cold and it hurts; and was still the same until the report. The patient wants to know if there was a certain time to wait for the symptoms and if she should go to see her doctor. No therapeutic measures taken as a result of the events. The outcome of the events strange taste in mouth; and smelling and tasting sauteed green onions and green peppers were recovering while other reported events were not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: FLUOXETINE; LATANOPROST; LEVOTHYROXINE SODIUM; PANTOPRAZOLE SODIUM; VALPROIC ACID

Current Illness: Gastrointestinal disorder; Optic neuritis (had for 7 years; in both eyes); Thyroid disorder (had probably 20 years or so)

ID: 1792611
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 10/16/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: feeling crappy; nausea; headache; equilibrium is off; fever; tired; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age (Age: 73; Unit: Unknown) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Lot number and Expiration date were not reported), via an unspecified route of administration on an unspecified date as dose 2, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced feeling crappy, nausea, headache, equilibrium is off, fever, and tired. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792612
Sex: M
Age:
State: UT

Vax Date: 02/27/2021
Onset Date:
Rec V Date: 10/16/2021
Hospital:

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

Lab Data: Test Date: 2021; Test Name: heart beat; Result Unstructured Data: Test Result:was skipping around 68-78; Test Date: 2021; Test Name: Oxygen; Result Unstructured Data: Test Result:skipping around

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: his arm was sore at the site, swelling and pain more profound; his arm was sore at the site, swelling and pain more profound; swelling and pain more profound and sooner, knot in the arm; arthritic knees and joints became more painful,painful and went down in to the hip and left thigh muscles; lower left back got painful; painful and went down in to the hip and left thigh muscles; heart and lungs heart a few days after the second shot; his heart and lungs heart a few days after the second shot and had a strange feeling in his lungs; night sweats; heart beat was skipping around 68-78 and his oxygen was skipping around; had a headache on the top of his head; he has PVC; illusion of a spider walking on the wall; pain in the left arm bicep; his oxygen was skipping around; This is a spontaneous report from a contactable consumer (patient himself). A 80-year-old male patient received second dose of BNT162B2 (BNT162B2, Solution for injection, Batch/Lot number EL9264), via an unspecified route of administration on 27Feb2021 as dose 2, single for COVID-19 immunization. The patient's medical history included pulmonary fibrosis and chronic pulmonary obstructive disease (COPD), had mini strokes and had heart surgery for blood clots to his brain in 2008. The patient's concomitant medications were not reported. The patient received first dose of BNT162B2 (BNT162B2, Solution for injection, Batch/Lot number EN5318), via an unspecified route of administration on 06Feb2021 as dose 1, single for COVID-19 immunization. Patient stated that Pfizer safety sent him a survey form on 10Feb2021 for the reactions that he had to the first dose of the Pfizer Covid-19 vaccine on 6Feb2021, lot number EN5318.The patient stated that the vaccine card had May21 on it and wanted to know if that was the expiration date. He stated that he had 9 symptoms after the first dose reported that his heart hurt, arm sore, lungs felt funny and airy but could breathe really good, really bad frontal headache and the top of the head that were two real strong headaches that lasted quite a while, change in smell for several days and neck pain. Patient stated he was in terrible pain lying in the bed due to thirty things wrong with him and he is terminally ill, and his hearing and eyes are no good and he is old. After the second shot, on unspecified date in 2021, his arm was sore at the site, swelling and pain more profound and sooner, knot in the arm, arthritic knees and joints became more painful, illusion of a spider walking on the wall, pain in the left arm bicep, lower left back got painful and went down in to the hip and left thigh muscles and had headaches. The patient stated that his heart and lungs heart a few days after the second shot and had a strange feeling in his lungs he had night sweats and got drenched but this is a symptom of a heart problem which he has. The patient stated his heartbeat was skipping around 68-78 and his oxygen was skipping around. The patient stated that he has PVC. The patient stated he had a headache on the top of his head. The patient underwent lab tests and procedures which included heart rate: was skipping around 68-78 on 2021, oxygen saturation: skipping around on 2021. The outcome of the events was unknown. Follow-up (17Jun2021): Follow-up attempts completed. No further information expected. Follow up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1792613
Sex: M
Age:
State: IL

Vax Date: 03/24/2021
Onset Date: 03/25/2021
Rec V Date: 10/16/2021
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: lymph nodes in arm pit swollen (about half the size of a softball); Fatigue/tired; Slight fever; heavy legs; achy, sore; Flu-like symptoms; he was warm and flushed; feeling bad; This is a spontaneous report from a contactable consumer or other non-healthcare professional (patient). A 52-year-old male patient received BNT162B2 (PFIZER-BIOTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: ER8733) via an unspecified route of administration, administered in arm left on 24Mar2021 at 11:00 (at the age of 52 years old) as dose 1, single for COVID-19 immunisation. Medical history included surgery (also reported as the patient had 4-and-a-half-hour surgery and gave blood thinners), prostate cancer, prostatectomy (recovering, 03Mar2021, also reported as 4 weeks ago), incontinence and erectile dysfunction. Concomitant medication included tadalafil (CIALIS, taking a low dose) taken for prostatectomy from 13Mar2021 and ongoing. On 25Mar2021, the patient experienced lymph nodes in arm pit swollen (about half the size of a softball, discovered the node when he went to take a shower), fatigue, slight fever, heavy legs, achy, sore, and tired, flu-like symptoms, warm and flushed, feeling bad (about 24 hours later). The patient stated that he hasn't done anything today because movement makes it worse. Patient prior vaccinations within 4 weeks were reported as none and adverse events following prior vaccination reported also as none. The adverse events did not result to emergency room or physician office visit. The outcome of the events lymph nodes in arm pit swollen and fatigue was recovering; outcome of warm and flushed, feeling bad was unknown; outcome of all the other events was recovered on 26Mar2021. No follow-up attempts are possible. No further information is expected.

Other Meds: CIALIS

Current Illness:

ID: 1792614
Sex: F
Age:
State:

Vax Date: 03/10/2021
Onset Date: 03/01/2021
Rec V Date: 10/16/2021
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: itching / scratchy / head is itchy where her hairline is; some little pimples, kind of like a rash; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, Lot number was not reported), via an unspecified route of administration on 10Mar2021 as dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On Mar2021, the patient experienced itching / scratchy / head is itchy where her hairline is; and some little pimples, kind of like a rash. It was further reported that she was calling because on the 10th she got her vaccine and a couple days ago she had itching and some little pimples, kind of like a rash. It was reported that it was scratchy like a mosquito bite. She has some on her arms, her stomach, her back, her legs and her head is itchy where her hairline is. The caller wanted to know what to do since tomorrow was her due for her second dose. She asked if she needed to cancel it or get the second vaccine. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1792615
Sex: F
Age:
State: MN

Vax Date: 03/16/2021
Onset Date: 03/18/2021
Rec V Date: 10/16/2021
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: This is a spontaneous report from a contactable nurse (patient). A 79-year-old female patient received the 1st dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, solution for injection, batch/lot# EN6207), at the vaccination age of 79, via an unspecified route of administration, in left arm (reported as left upper arm), on Mar 16, 2021, at 13:30, single dose, for COVID-19 immunization. The patient's medical history and concomitant medications: none. The patient did not receive any other vaccine within 4 weeks prior to COVID-19 vaccine. On Mar 18, 2021, patient experienced rash on her upper left arm, chest, back and neck (just the left-side). The outcome of the event: recovering. No follow-up attempts possible. No further information expected.

Other Meds:

Current Illness:

ID: 1792616
Sex: F
Age:
State: NY

Vax Date: 03/10/2021
Onset Date:
Rec V Date: 10/16/2021
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: Patient experiencing allergy symptoms, sneezing and body aches; is afraid to go to appointment for second vaccine tomorrow; Patient experiencing allergy symptoms, sneezing and body aches; is afraid to go to appointment for second vaccine tomorrow; Patient experiencing allergy symptoms, sneezing and body aches; is afraid to go to appointment for second vaccine tomorrow; This is a spontaneous report from a contactable consumer (Reporter is calling on behalf of her aunt). A unspecified age of female patient received BNT162B2 (Pfizer- BioNTech COVID 19, solution for injection, Batch/lot number: Not Provided) via an unspecified route of administration on 10Mar2021 as dose 1, single for COVID-19 immunization. The patients medical history and concmittant medications were not reported. On unspecified date, the patient experiencing allergy symptoms, sneezing and body aches; is afraid to go to appointment for second vaccine tomorrow. Reporter states she is going to tell the patient to just go next week for second vaccine. Reporter is calling on behalf of her aunt, who received the first dose of Covid-19 vaccine on 10Mar and had a scheduled appointment for a second dose due tomorrow, 31Mar. She mentioned that her aunt has an allergy and body ache yesterday so she cannot go tomorrow. Asked if she can cancel her appointment tomorrow and go next week. The oucome of events was unknown. Follow-up (05Apr2021): This is a follow-up spontaneous report received in response to the mail trail sent regarding the confirmation below mentioned query. The response included: Query: Please see the attached source document with a medical inquiry. AER# 2021361419.Response: This is to confirm receipt of inquiry. Please see case in GRACE, INT-# Follow-up (30Jun2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am