VAERS 2021 Database www.vaers.hhs.gov

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

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

COVID19 Lot Number

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

Incidents per State

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

ID: 1648772
Sex: F
Age:
State: MN

Vax Date: 03/11/2021
Onset Date: 03/11/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: My left cheek started tingling and then it moved across my whole face and was numb for 3 hours; My left cheek started tingling and then it moved across my whole face and was numb for 3 hours; This is a spontaneous report from a contactable consumer or other non hcp. A 50-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot Number: EN6208) via an unspecified route of administration, administered in Arm Left on 11Mar2021 16:45 (at the age of 50-years-old) as dose 1, single for COVID-19 immunization. Medical history included Known allergies: PCN (drug hypersensitivity) from an unknown date and unknown if ongoing. Patient did not test for COVID prior vaccination nor tested post vaccination. She did not receive other vaccine in four weeks. She had other unspecified medications in two weeks. On 11Mar2021 17:00 the patient experienced my left cheek started tingling and then it moved across my whole face and was numb for 3 hours. No treatment received for events. The outcome of the events was reported as recovered on 11Mar2021 20:00. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1648773
Sex: F
Age:
State: MS

Vax Date: 01/29/2021
Onset Date: 01/30/2021
Rec V Date: 08/28/2021
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: felt it in my heart; This is a spontaneous report from a contactable consumer (patient) via COVID-19 Adverse Event Self-Reporting Solution (COVAES). A 57 years old non-pregnant female patient (not pregnant at the time of vaccination) received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; Lot Number: EL9261) via an unspecified route, administered in Left Arm on 29Jan2021 at 09:15 AM (57-year-old at time of vaccination) as Dose 1, single for Covid-19 immunization. The patient's medical history included High blood pressure and rapid heart rate. Meds control it. The patient had no known allergies. The patient's concomitant medications were not reported. Facility type vaccine was reported as Administration facility. The patient had no covid prior vaccination. The patient was not Covid tested post vaccination. The patient had no other vaccine within four weeks of Covid-19 vaccination. On 30Jan2021 ay 09:15 AM, (it was reported that 20 minutes after vaccination), the patient had felt it in her heart. The patient had not received any treatment medications for the resulted events. The outcome of the event was recovered on an unknown date in 2021. No follow-up attempts are possible. No further information was expected.

Other Meds:

Current Illness:

ID: 1648774
Sex: F
Age:
State: NY

Vax Date: 03/09/2021
Onset Date: 03/09/2021
Rec V Date: 08/28/2021
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 Name: Blood test; Result Unstructured Data: Test Result:Presence of antibodies; Comments: I had a recent blood test confirming the presence of antibodies & I believe that my severe reaction was intensified due to their presence; Test Date: 20200404; Test Name: COVID-19; Result Unstructured Data: Test Result:Positive

Allergies:

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

Symptoms: Fever; Chills; Headache; fatigue; Fever, chills, headache, fatigue, body aches, nausea, stomachache, sore arm, insomnia, tachycardia, throbbing teeth. I had a recent blood test confirming the presence of antibodies & I believe that my; stomachache; Sore arm; Insomnia; Tachycardia; Throbbing teeth; Body aches; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 65-years-old female patient (patient was not pregnant at the time of vaccination) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EN6206, Expiration date: unknown) via an unspecified route of administration, administered in right arm on 09Mar2021 at 12:00 pm (age at vaccination was 65 years) as dose 2, single for COVID-19 immunization. The patient's medical history included hypertension from an unknown date and COVID-19 from 04Apr2020 to an unspecified date (patient's positive COVID test was almost a year ago on 04Apr2020). The patient did not have any known allergies. Concomitant medications the patient received in 2 weeks included candesartan, atorvastatin, hydrochlorothiazide (MICROZIDE [HYDROCHLOROTHIAZIDE]), clonazepam (KLONOPIN) all taken for an unspecified indication. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EL9266, Expiration date: unknown) via an unspecified route of administration, administered in right arm on 16Feb2021 at 13:00 pm (age at vaccination was 65 years) as dose 1, single for COVID-19 immunization. The facility where the most recent COVID-19 vaccine was administered was other. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. The patient underwent lab test which included Sars-cov-2 test: positive on 04Apr2020. Since the vaccination, the patient has not been tested for COVID-19. On 09Mar2021 at 16:30 pm, the patient experienced fever, chills, headache, fatigue, body aches, nausea, stomachache, sore arm, insomnia, tachycardia, throbbing teeth. She had a recent blood test confirming the presence of antibodies & she believed that her severe reaction was intensified due to their presence. She took Acetaminophen & Ibuprofen round the clock for the next 48 hours. The patient received treatment with over the counter medications. The outcome of the events was resolving. No follow-up attempts are possible. No further information is expected.

Other Meds: CANDESARTAN; ATORVASTATIN; MICROZIDE [HYDROCHLOROTHIAZIDE]; KLONOPIN

Current Illness:

ID: 1648775
Sex: F
Age:
State: NY

Vax Date: 03/09/2021
Onset Date: 03/09/2021
Rec V Date: 08/28/2021
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: numbing and tingling on face, hands lips and tongue; numbing and tingling on face, hands lips and tongue; This is a spontaneous report from a contactable consumer (patient). A 61-years-old female non-pregnant patient received bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, Solution for injection), via an unspecified route of administration, administered in Arm Left on 09Mar2021 11:00 (at the age of 61-years-old) (Batch/Lot number was not reported) as dose number unknown. single for COVID-19 immunisation. Medical history included asthma and allergy to metals and dyes from an unknown date and unknown if ongoing known allergies. Concomitant medications included bupropion hydrochloride (WELLBUTRIN), atomoxetine hydrochloride (STRATTERA), salbutamol (VENTOLINE) and budesonide, formoterol fumarate (SYMBICORT) taken for an unspecified indication, start and stop date were not reported. The patient had not received other vaccine in four weeks, the patient had no prior vaccination and covid test post vaccination. The patient experienced numbing and tingling on face, hands lips and tongue on 09Mar2021 11:00. The patient received treatment of antihistamine in response to event. The clinical outcome of events was unknown. No follow-up attempts are possible; Information about lot/batch number cannot be obtained.

Other Meds: WELLBUTRIN; STRATTERA; VENTOLINE [SALBUTAMOL]; SYMBICORT

Current Illness:

ID: 1648776
Sex: M
Age:
State:

Vax Date: 02/27/2021
Onset Date: 02/27/2021
Rec V Date: 08/28/2021
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: 20210227; Test Name: heart rate; Result Unstructured Data: Test Result:Elevated

Allergies:

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

Symptoms: Elevated heart rate after second dose. Will not go back to normal.; This is a spontaneous report from a contactable consumer or other non HCP (patient reported for self). An elderly male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EE9265, Expiry date: unknown), via an unspecified route of administration, administered in Left arm on 27Feb2021 as dose 2, single for COVID-19 immunization. The patient had earlier received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EE9265), via an unspecified route of administration, administered in Left arm on 05Feb2021 as dose 1, single for COVID-19 immunization. Medical history reported as none. Patient had no known allergies. The concomitant medications. was not reported. On 27Feb2021, the patient experienced elevated heart rate after second dose, will not go back to normal. The patient underwent lab tests and procedures which included heart rate was elevated on 27Feb2021. Patient was not tested for COVID post vaccination. Patient did not receive any treatment. The clinical outcome of event was reported as not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1648777
Sex: F
Age:
State: NC

Vax Date: 02/07/2021
Onset Date: 02/08/2021
Rec V Date: 08/28/2021
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: 20210210; Test Name: Nasal Swab; Test Result: Negative

Allergies:

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

Symptoms: Chest pain. Been 30 days; This is a spontaneous report from a contactable consumer or other non hcp (Patient). A 67-years-old non pregnant female patient received second dose of bnt162b2 (BNT162B2, PFIZER-BIOTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration, administered in Arm Right on 07Feb2021 12:00 AM (Age at vaccination: 67-years-old) as single dose for covid-19 immunization. Medical history included Factor V, allergies to Sulpha all from an unknown date and unknown if ongoing. Concomitant medications were not reported. Historical vaccine included first dose of bnt162b2 in arm right on 17Jan2021 12:00 AM (Age at vaccination: 67-years-old) for covid-19 immunization, patient previously took cipro [ciprofloxacin] and experienced drug hypersensitivity. Patient did not receive other vaccine in four weeks. Patient was not diagnosed with covid prior to vaccination. On 08Feb2021 12:00 AM patient experienced Chest pain. Been 30 days. Adverse event resulted in Doctor or other healthcare professional office/clinic visit. Patient did not receive any treatment for the events. Patient was tested for covid since the vaccination. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 10Feb2021. The outcome for the event was reported as not resolved at the time of this report. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1648778
Sex: F
Age:
State: MI

Vax Date: 03/04/2021
Onset Date: 03/06/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 20210311; Test Name: Urinalysis; Result Unstructured Data: Test Result:positive for a UTI

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: all day in bed, couldn't get up; lost 3lbs; UTI; no appetite/Does not have the same appetite she normally does; extreme fatigue; chills "now and then"; nausea; Slept all day; back and stomach muscle aches; back and stomach muscle aches; Fever; Felt icky; This is a spontaneous report from a contactable consumer (patient). A 79-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN6202) (79-years-old at the time of vaccination) via an unspecified route of administration, administered in arm left on 04Mar2021 as dose 1, single for COVID-19 immunization. The patient medical history was not reported. As concomitant medications patient took quite a bit of medications, like 35 pills a day and a lot of loperamide hydrochloride (IMODIUM). Patient reported that she had the first dose on 04Mar2021 (Thursday) and reported that the next day she felt fine up until 06Mar2021 (Saturday) at supper time, she felt icky. She said that on 07Mar2021 (Sunday) when she woke up at like 1000, she slept all day, had back and stomach muscle aches that she treated with Motrin, had no appetite, extreme fatigue, chills, fever, and nausea. She said that she was taking Zofran and took 1 Phenergan for the nausea. She did not eat almost all day on Sunday. She said that she sells asleep at about 11:00 on Sunday and woke up at 16:30. She zonked right out. She said that she had extreme fatigue. She did not know if she had a reaction if she can have a delayed reaction from the vaccine. Since Sunday, every day has been a little better. She said that on an unknown date she lost 3lbs and she only weighs 80lbs now. She reported that she does not have the same appetite she normally does. This morning she was a little nauseous and had to lay down and stated that she did not want to throw up. She said that her nausea and her poor appetite were better, but they were not good yet. The last couple of days her urine was darker than normal. She said that she thought it was a UTI. She called her doctor and was sent to have a urine sample test (urinalysis) on 11Mar2021, and it came back positive for a UTI. She said that she has not picked up the antibiotic for the UTI yet. Caller said that she noticed the darker urine on either Thursday or Wednesday. She said that the urine was a little darker than tea coloured. She said that she felt like she carried something real heavy and on Sunday she could hardly move. She said that she was not eating like she should be and was still a little nauseated and her appetite was not good yet. Caller stated that it had improved a little bit. Caller said that she could hardly dial or text because she was shaking so bad from the chills. Then she would feel warm. She stated that the chills come and go, but have improved. She stated that she has not taken her temperature. She wondered if the UTI was causing her stuff now. She said that she can't pick up her Antibiotic for the UTI until tomorrow. Outcome was not resolved for the event UTI, unknown for fever and lost 3lbs and the outcome for event back and stomach muscle aches was resolved on 10Mar2021 and outcome for rest events was resolving. No follow-up attempts are possible. No further information is expected.

Other Meds: IMODIUM

Current Illness:

ID: 1648779
Sex: F
Age:
State: OH

Vax Date: 02/24/2021
Onset Date: 02/24/2021
Rec V Date: 08/28/2021
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: Heart rate; Result Unstructured Data: Test Result:high and was fast paced on the pulse ox

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: Her heart rate high and was fast paced; aggravation from the vaccine went down her arm across her shoulder to her other shoulder and arm; This is a spontaneous report from a contactable consumer (patient, self-reporting). A 77-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EM9809, Expiry date was not reported), dose 1 via unspecified route of administration on left arm on 24Feb2021 as single dose for COVID-19 immunization. The patient's medical history Diabetes, Triple bypass since 2019 (Ongoing) were reported. The patient concomitant medications were not reported. Reported stated that her first dose was on 24Feb2021. She said that she did not even feel the shot that she had on Wednesday 24Feb2021 and said that by Thursday, the aggravation from the vaccine went down her arm across her shoulder to her other shoulder and arm. It was really strong. On Friday 26Feb2021, her heart started to act up and act wonky. She clarified that her heart rate was high and was fast paced on the pulse ox. She tried to call her primary care physician but could not get a hold of them. She said that she controlled it herself. Caller said that she has had a triple heart bypass in the past. She was due on 24Mar2021 to get her second dose. She said that everyone says that it was worse. With her history of the AFib, was this going to cause undue episode or what is the experiences that have been reported. She said that she never had aggravation that travelled from one arm to her shoulder and across to her other shoulder and arm before with any other vaccine. Caller stated that she took aspirin to treat her heart rate. The patient developed aggravation from the vaccine went down her arm across her shoulder to her other shoulder and arm started on 24Feb2021 and stopped on 25Feb2021 and Her heart rate high and was fast paced start date 26Feb2021 and stopped on 26Feb2021 was updated. The outcome of the event was recovered. No follow-up attempts are possible. No further information expected.

Other Meds:

Current Illness: Diabetes (Verbatim: Diabetes)

ID: 1648780
Sex: F
Age:
State: NM

Vax Date: 02/26/2021
Onset Date: 02/26/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: Approximately 5 minutes post vaccination patient had numbness from shoulder to hand; This is a spontaneous report from a contactable other healthcare professional. A 53-years-old female patient (pregnant: unknown) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EN6203), via intramuscular on 26Feb2021 at 15:30 (at the age of 53-years-old) as dose 1, single for COVID-19 immunization at public health clinic/veterans administration facility. Medical history included MS (multiple sclerosis). The patient's concomitant medications were not reported. No known allergies. It was unknown if the patient received any other vaccine in four weeks or other medications in two weeks. It was unknown if the patient had COVID prior to vaccination and unknown if tested for COVID post vaccination. On 26Feb2021 at 15:35, approximately 5 minutes post vaccination patient had numbness from shoulder to hand. Numbness improved approximately 15 minutes post vaccination. Continued observation for additional 15 minutes. The patient was discharged at 15:38. The patient did not receive treatment for the adverse event. The outcome of event was resolved on an unspecified date in 2021. No follow up attempts are possible; no further information expected.

Other Meds:

Current Illness:

ID: 1648781
Sex: F
Age:
State:

Vax Date: 03/02/2021
Onset Date: 03/01/2021
Rec V Date: 08/28/2021
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: Chronic Knee pain; This is a spontaneous report from a contactable consumer (patient). A 73-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 02Mar2021 as dose number unknown, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient would like to know if it was fine for him to take Aleve or aspirin. The patient had chronic Knee pain in Mar2021. The patient would also wanted to know if she could take steroid injection for knee pain. The outcome of event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1648782
Sex: F
Age:
State: NC

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Name: Blood pressure; Result Unstructured Data: Test Result:High

Allergies:

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

Symptoms: Strong pulse; Tinnitus; Elevated blood pressure; This is a spontaneous report from a contactable consumer (Patient). A 63-year-old female patient received BNT162B2 (COMIRANTY; Formulation: Solution for injection; Lot number: Unknown, Expiration date: was not reported) via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. Medical history included high blood pressure, anxiety and overweight. Concomitant medications were not reported. On an unspecified date, patient experienced strong pulse, tinnitus and elevated blood pressure. The patient underwent lab tests and procedures which included Blood pressure: High on an unspecified date. Patient also reported she didn't know if the symptoms could be because she was nervous. Before getting the vaccine, she asked her doctor if it was okay for her to get it, since she has high blood pressure (caller stated she takes medication for this and it is under control), anxiety and overweight, and doctor said it was okay. If the second dose is stronger than the first one, should she still get the second dose?. The outcome of events were unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1648783
Sex: M
Age:
State: CA

Vax Date: 03/10/2021
Onset Date: 03/01/2021
Rec V Date: 08/28/2021
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: Nausea; had little hives here and there; vomiting; redness on wrists, hands; inflammation; This is a spontaneous report from a contactable consumer (patient). A 22-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 10Mar2021 at 15:00 hours (Batch/Lot Number: EN6204) as DOSE 1, SINGLE (at the age of 22-years-old) for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient's history of all previous immunization with the Pfizer vaccine considered as suspect was reported as none. Additional Vaccines Administered on Same Date of the Pfizer Suspect was reported as none. The patient's medical History (including any illness at time of vaccination) was not reported. The patient's family History was not reported. On 11Mar2021, the patient experienced nausea, on an unspecified date in Mar2021 experienced vomiting, redness on wrists, hands, and inflammation. It was not reported whether the patient had admission to the hospital or received any treatment due to the events nausea, vomiting and redness on wrists, hands. On 11Mar2021, the patient started to feel nauseated and then had little hives here and there. The patient had not seen any new ones on the day of reporting and the inflammation seemed to have gone down; they were not as red on the day of reporting. The patient was more nauseated on the day of reporting. The patient queried for how long these side effects tend to last and Mentioned that this was the first vaccine reaction he has ever had and the first time he has had to call in to report anything without his parents doing it for him. The patient also queried whether he should still get his 2nd dose and for any recommendations on treatment for the symptoms. The patient had no relevant tests reported. The adverse events did not require a visit to physician or emergency room. The patient had no prior Vaccinations (within 4 weeks). The patient was recovering from the events inflammation and had little hives here and there; had not recovered from the event nausea and the clinical outcome for other events was unknown. Follow-up attempts are needed. Follow-up (14May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1648784
Sex: F
Age:
State: FL

Vax Date: 02/27/2021
Onset Date:
Rec V Date: 08/28/2021
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: Medical Information Potential AE; Pain and swelling in her breast; Pain and swelling in her breast; Stated that her right nipple was uncomfortable; Stated that her right nipple was swollen; It feels like a lymph node; This is a spontaneous report from a contactable consumer (patient). A 65-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration, administered in Arm Right on 27Feb2021 (at the age of 65-year-old) as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced medical information potential AE on an unspecified date. The patient reported that she developed pain and swelling in her breast that has been ongoing for 3 days. She stated that she knew there are lymph nodes in the area but wanted to know if this was normal and how to treat the same. Caller also stated that a couple of days ago her right nipple was uncomfortable and was now swollen. Stated that it felt like a lymph node. She wanted to know if possible if it could be a lymph node. Seriousness of the events was reported as non-serious. The outcome of events was unknown. Information on the lot/batch number has been requested. Follow-up (14May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1648785
Sex: M
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
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: Urinary Tract infection; arms was sore in that area; headache; This is a spontaneous report from a contactable consumer (patient). A 90-year-old male patient received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number and expiry date was not reported), via an unspecified route of administration on an unknown date in 2021 (age at vaccination: 90-year-old) as dose 1, single for covid-19 immunisation. Medical history included macular degeneration from an unknown date and unknown if ongoing (he was almost blind and don't drive because of his macular degeneration, he had for years. His eye problem started 30 something years ago when he was 50) and kidney stones (has tendency to get kidney stones). The patient's concomitant medications were not reported. The patient received his first dose 2 weeks ago on an unknown date and it took him a long time to get the vaccine. Next Friday on 19Mar2021 he was scheduled for his 2nd dose. Caller stated, he went to his doctor and got antibiotics which he would start today. He got an urinary tract infection. He has tendency to get kidney stones, so he has to watch what he eat. This was not unusual. She had quite a few. The first was the worst; almost all of them he has passed. Normally he drink water and he would pass, none were the same, he would to get an ultrasound. It took him a long and long time to get the vaccine. His side effects: first day his arms was sore in that area (it hurt a little bit in the morning and 6-7 hours later he didn't even know it was there). Before he got his flu shot he needed to exercise the arm. He had a little headache and that went away. His pharmacist said it would be alright with his antibiotic but he wanted to make sure. The outcome of the event urinary tract infection was unknown and other events recovered on an unspecified date in 2021. No follow-up attempts are completed; information about lot/batch number cannot be obtained. No further information expected.

Other Meds:

Current Illness:

ID: 1648786
Sex: F
Age:
State: NC

Vax Date: 03/10/2021
Onset Date: 03/10/2021
Rec V Date: 08/28/2021
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: my face on right side was numb; tasted something in my mouth like metal; This is a spontaneous report from a contactable consumer (Patient). A 58-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN6203), via an unspecified route of administration on 10Mar2021 at 12:00 (at the age of 58-year-old), as dose 1, single in right arm for COVID-19 immunization at Pharmacy/drug store. The patient's medical history included hypothyroidism. Patient had no known allergies. Concomitant medications in two weeks included levothyroxine sodium (LEVOTHYROXIN); and bupropion hydrochloride (WELLBUTRIN), all taken for an unspecified indication, start and stop dates were not reported. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 10Mar2021 at 12:15, 15 minutes after the first dose of vaccine, the patient's face on right side was numb, tasted something in her mouth like metal. Patient was fine for the first 15 minutes after vaccination. Once she was in the car to leave, she immediately tasted something in her mouth like metal and then her face on right side was numb, near right ear, right cheek, jawline, and tongue. There was no swelling. Sensation subsided by next morning. Patient felt like there was still be some numbness but very mild. Patient was hesitant to take second dose. No treatment was received for the events. The patient had no COVID prior vaccination and was not tested COVID post vaccination. The clinical outcome of both the events was reported as unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: LEVOTHYROXIN; WELLBUTRIN

Current Illness:

ID: 1648787
Sex: F
Age:
State: MN

Vax Date: 03/05/2021
Onset Date: 03/05/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 20210305; Test Name: Blood pressure; Result Unstructured Data: Test Result:170 over something; Test Date: 20210305; Test Name: Blood pressure; Result Unstructured Data: Test Result:140-something or 130-something; Test Date: 20210305; Test Name: pulse; Result Unstructured Data: Test Result:went up

Allergies:

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

Symptoms: joint pain in her wrist, hands, and hips; she slept for a long time; blood pressure was really high; Pulse went up; extreme pain in her chest; couldn't raise her arm high at all; was very tired; This is a spontaneous report from a contactable consumer or other non hcp. An 85-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 05Mar2021 at 12:30 (Batch/Lot number was not reported) as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history major stroke and she was told that should be in a type of home from that. She has been very fortunate. They got her in the hospital quick and she had the best doctor around for the stroke. They said that she is a miracle person. She didn't have to have therapy after her stroke and she had a major stroke. She also has had three heart procedures. They're amazed and her health was great, her heart and lungs are great. Confirmed with caller that the major stroke and heart procedures had occurred prior to her COVID vaccine. she had just seen her doctor the day before and in fact she is waiting to hear results from him. She had lab work and a urine analysis done on 04Mar2021 which she hasn't done for a while. She was waiting for those results. Confirmed with caller that these tests were done prior to her COVID vaccine. Patient from a family of 10 children and out of 6 boys, there was only 1 left. That one brother left has had strokes, heart surgery, heart attacks and basic life that was just buying time for him. One of her brothers was killed, he was a pilot and they directed him into a mountain. A lot of people in her family have died suddenly of heart issues, her mother and grandmother died. She was the only 1 of the 4 girls who have had any problems with heart issues. One brother, at 47 years old had a massive heart attack. Another one died when he had gone to the doctor the day before because he was having heart attack signs. The doctor sent him home to take Aspirin and he was found dead the next morning. Reporter stated that, the patient was going to be 86 years old soon and her sister who is 93 years old got the COVID virus. Her sister-in-law and her family got COVID. The caller has been staying in her house for a year. She hasn't seen her sisters in a year and when she did see one of her sisters for the first time in a year, her sister didn't know it was her. The caller has long hair now and usually she has a pixie cut. Also, her friend she saw just stared at the caller and said she didn't know who she was and they have known each other for 47 years. And that was also because of her long hair. She said so the reason she got her COVID vaccine was because she doesn't want to get this COVID virus. Her sister was fortunate and the caller pushed her sister into going to the hospital and the doctor told the caller that had her sister not gotten there when she did, she wouldn't of made it. The caller pushed her to go and made her sister's son take the sister to the hospital. Another had went in to the doctor and he was told that he was just having issues with his gallbladder and he died that night. So what she experienced was very relevant with her family history. It is kind of selfish to think this, but she hopes she goes that way too. There are very many heart issues in her family. Patient brother took and she says she does not have to provide. It was years ago. They gave him a sticker for his car so that he would not have to walk as far. He had heart surgeries and had all the symptoms at that time he went to the doctor. Even his legs were hurting but they told him to come back the next day, take Aspirin that night, and gave him a sticker for his car. His wife found him dead the next morning. Her 47-year-old brother had 10 kids, he was in the hospital and they had let him go home for his and his wife's birthday, and then he died in his wife's arms.Her heart has been fine since they cleaned out her arteries. It is amazing. She asked her doctor if he attributes that to all of the medications she takes and he said that helps, but mostly is it attributed to her attitude. Her attitude plays such a big role in her health, she was told. Patient had gotten her COVID vaccine then was told to wait 15 minutes. She was sitting in front of where the nurses was and daughter took one look at the reporter and asked if she was okay. The reporter told her daughter that she was not okay and that she was having really bad chest pain. The patient had extreme pain in her chest then the nurses came in with a wheelchair and took her into a cubicle at the facility. She said her blood pressure was really high, her pulse went up, and she doesn't know how long she was there. She heard someone ask if they should call first responders and a doctor, or someone, said to wait a minute and just see how the reporter was doing. She has had 3 heart surgery procedures, but not open heart surgery, and she was with her doctor the day before and he said that her heart was good, there were no fast beats and it sounded good. She was told to always carry nitroglycerin with her and she told the nurses at the facility that she was at that she had it and she took the nitroglycerin since that was what she was supposed to do. Within a few minutes the pain had left. Patient was not visit to the Emergency Room or Physician Office but she had heard one nurse ask should they call in the first responders and there was another woman who came in a couple times into the cubicle that the caller was in and asked how the caller felt and said to just wait a few minutes there. Someone said that they probably should of taken the caller to the emergency room or called the first responders but the caller doesn't know if they should of because she was getting better. She has never had a heart attack before, so she doesn't know what it feels like. Her brother has had them before and he asked her if it felt like a truck was crushing her chest and she said it didn't feel like that, but it hurt a lot. She could breathe and it wasn't like that at all. She said, how do you describe hurt? It is just like "ouch!" But her daughter could see it on the caller's face and her daughter knew right away that something wasn't right. Her daughter asked her to describe the pain she was feeling and she told her daughter that she can't and the caller has never had a heart attack before so she was unsure if that was the type of pain she was having. This morning she was thinking about the pain she had and she said that previously she had undergone a process that was being done to her heart where they were trying to get an artery unplugged. It was an experimental thing. She told them that she didn't want to be completely out, she wanted to know what was happening. All of a sudden she was in pain and they said that pain happened because they just cleared her artery. She was in a 2 year study for that and it worked therefore she didn't have to have open heart surgery. She says that pain was what the pain was like after her COVID vaccine. On 05Mar2021, it was confirmed that her blood pressure and her pulse went high, right after her COVID vaccine and then the nurses took her into the other room to check these. She was not dizzy, but of course she didn't stand up since she was in a wheelchair. Caller was unable to remember the numbers for her pulse. Her blood pressure was 171 over something. She told the nurse to just wait and her blood pressure will come down so they waited and it came down. The lowest it had gotten there was 140-something or 130-something, but it took a long time. Caller says that the chest pain, high blood pressure, and the high pulse all ended on the same day, 05Mar2021. She said after she sat for a while a nurse walked her to her car to be sure that the caller was fine when she left the facility. She had no further issues after that, she was tired when she got home, but no problems after that. The pain went and it didn't come back. Caller confirms that she recovered completely. She told them her blood pressure

Other Meds:

Current Illness:

ID: 1648788
Sex: F
Age:
State: NY

Vax Date: 02/14/2021
Onset Date: 02/16/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 20210304; Test Name: Covid test; Test Result: Negative

Allergies:

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

Symptoms: drastic deteriation of eye sight; extreme chest pain; extreme lungs pain; hard to breathe; loss of appetite; feeling of numbness in limbs; extreme anxiety; insomnia; dizziness; mild headaches; mild chills; mild brain fog; stiff neck; stiff jaws; feeling hyper activated; This is a spontaneous report from a contactable other hcp (patient) reported for herself that . A 57-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/Lot Number: EL9266), dose 2 via an unspecified route of administration, administered in Arm Left on 14Feb2021 (Age at vaccination 57-years-old) as DOSE 2, SINGLE for covid-19 immunization. Medical history included mitral valve prolapse, anxiety, presyncope from an unknown date and unknown if ongoing. Patient had no known allergy. Concomitant medications included estradiol (VIVELLE DOT), estradiol (ESTRACE) taken for an unspecified indication, start and stop date were not reported. Patient previously took first dose of BNT162B2 (Lot number=EL9262), in Arm Left, on 25Jan2021 at 08:15 (Age at vaccination 57-years-old), for COVID-19 immunization. Patient did not receive other vaccine in four weeks of vaccination. Patient was not diagnosed with COVID-19, prior vaccination. Patient has been tested for COVID-19, post vaccination. On 16Feb2021 the patient experienced drastic deteriation of eyesight, extreme chest/lungs pain, hard to breathe, loss of appetite, feeling of numbness in limbs, extreme anxiety, insomnia, dizziness, for 10 days of second dose of vaccine. its almost one month, I am still experiencing, extreme anxiety, mild headaches, odd mild chills, mild brain fog, numbness in limbs, stiff neck, jaws, feeling hyper activated. The adverse events resulted in Doctor or other healthcare professional office/clinic visit. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 04Mar2021. No treatment received for adverse events. Outcome of the events was not recovered, No follow-up attempts are possible. No further information is expected.

Other Meds: VIVELLE DOT; ESTRACE

Current Illness:

ID: 1648789
Sex: F
Age:
State: CA

Vax Date: 02/26/2021
Onset Date: 02/26/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 20210226; Test Name: heart pulse; Result Unstructured Data: Test Result:racing

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: heart pulse was racing; dizzy; This is a spontaneous report from a contactable consumer (patient herself). A 66-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number: EN6203, expiry date: unknown) via unspecified route of administration, in left arm on 26Feb2021 14:30 (age at vaccination: 66-years) as dose 1, single for Covid- 19 immunisation. Facility type vaccine was public health clinic/veterans administration facility. Patient was not pregnant at the time of vaccination. Patient was not diagnosed with covid prior to vaccination. She was not tested for covid since vaccination. Patients medical history included asthma, thyroid and known allergies of citrus and mold from an unspecified date and unknown if ongoing. Concomitant medication included flu vaccine as single dose on 10Feb2021 (in 4 weeks of covid vaccine), for unspecified indication. On 26Feb2021 2:30PM, immediately after receiving the Covid 19 vaccine, her heart pulse was racing, and she started to feel dizzy. The patient underwent lab test for heart rate on 26Feb2021, with results as racing. No treatment was given as a result of the adverse events. The outcome of event was recovered on an unspecified date. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1648790
Sex: F
Age:
State: VA

Vax Date: 02/01/2021
Onset Date: 02/02/2021
Rec V Date: 08/28/2021
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: Severe hives that started on my ears and then spread to face, neck and arms. It's continuing to spread down my legs; Pregnant at the time of vaccination: Yes; Pregnant at the time of vaccination: Yes; Pregnant at the time of vaccination: Yes; This is a spontaneous report received from a contactable consumer (patient). A 33-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, batch/lot number: EL 9264, expiry date: unknown), via an unspecified route of administration in the right arm on 01Feb2021 at 11:00 (at the age of 33-year-old), at dose 2, single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. the patient had no known allergies to medications, food, or other products. The historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EL3302) on right arm on 12Jan2021 (at the age of 33-year-old) at 12:00 PM as dose 1 for COVID-19 immunization. The patient was not diagnosed with COVID-19 prior to vaccination and was not tested for COVID-19 post vaccination. The patient did not receive any other vaccine within 4 weeks prior to BNT162B2 vaccine. The patient experienced severe hives that started on her ears and then spread to face, neck and arms. It was continuing to spread down her legs. It started on 02Feb2021 and is still going on 11Feb2021. The patient was pregnant at the time of vaccination on 01Feb2021. The date of last menstrual period was on 01Jan2021 and the gestation period was 4 week. The patient is due to deliver on 08Oct2021. The reporter assessed the events as non-serious. The adverse event resulted in the emergency room/department or urgent care. The patient received topical steroids and antihistamines for the events. Outcome of the event Pregnant at the time of vaccination: yes was not resolved and for other event was unknown.

Other Meds:

Current Illness:

ID: 1648791
Sex: F
Age:
State: WA

Vax Date: 03/12/2021
Onset Date: 03/01/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Full body numbness; Lack of coordination; Extreme exhaustion; Inability to focus; feel a faint generalized numbness but it is fading; This is a spontaneous report from a contactable consumer (patient).A 43-years-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EN6208),via an unspecified route of administration on 12Mar2021 at 08:15 (at the age of 43-years-old) as a dose 1, single for COVID-19 immunization. Medical history included HEDS (Hypermobile type Ehlers-Danlos syndrome) and scoliosis. The patient was not allergic, but sensitive to eggs, dairy, steroids, aspirin, ibuprofen. Concomitant medication(s) included cyanocobalamin (B12 [CYANOCOBALAMIN]); vitamin d [vitamin d nos] and ascorbic acid (VIT C). The patient previously took aspirin [acetylsalicylic acid] and ibuprofen and experienced drug hypersensitivity. The patient did not receive any other vaccine in four weeks. The patient was not diagnosed with COVID prior to vaccination. The patient was not tested for COVID post vaccination. On 12Mar2021 at 20:00, the patient experienced lack of coordination, extreme exhaustion, inability to focus, on 13Mar2021, around 2pm the patient experienced full body numbness and on an unspecified date in Mar2021, she experienced feel a faint generalized numbness, but it was fading. The patient reported that she experienced full body numbness climaxing around 2pm on 13Mar2021, the day after the injection. Also, lack of coordination, extreme exhaustion, inability to focus. It was 14Mar2021 and she still feel a faint generalized numbness, but it was fading, thankfully. The patient did not receive any treatment for adverse events. The patient was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: B12 [CYANOCOBALAMIN]; VITAMIN D [VITAMIN D NOS]; VIT C

Current Illness:

ID: 1648792
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Name: Temperature; Result Unstructured Data: Test Result:102.8

Allergies:

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

Symptoms: Temp of 102.8 a few hours after injection. This temp was relieved after a couple of hours without any medication.; This is a spontaneous report from a contactable consumer or other non healthcare professional. A adult female patient received bnt162b2 (BNT162B2), dose 1 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 unknown from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient experienced temperature of 102.8 a few hours after injection. this temperature was relieved after a couple of hours without any medication on an unspecified date with outcome of recovered. The patient underwent lab tests and procedures which included body temperature at 102.8. Follow-up (15Mar2021): This is a follow-up spontaneous report received from contactable consumer. This consumer reporting for female patient that, She became aware of the event on 8Mar2021. No follow-up attempts are needed; Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1648793
Sex: F
Age:
State: CA

Vax Date: 03/13/2021
Onset Date: 03/13/2021
Rec V Date: 08/28/2021
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: Numbing and tingling sensation in my thumb, pointer, and middle finger of my right hand.; Numbing and tingling sensation in my thumb, pointer, and middle finger of my right hand.; This is a spontaneous report from a contactable consumer (patient). A 39-year-old non pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number was not reported, Expiry date not reported) via an unspecified route of administration in Arm Right on 13Mar2021 11:00 (at the age of 39 years old) as dose 2, single for COVID-19 immunization. Medical history included bipolar 2 disorder, allergy to penicillin. Patient was not tested for COVID post vaccination Concomitant medication taken within two weeks of COVID vaccine included ibuprofen (IBUPROFEN) taken for an unspecified indication, start and stop date were not reported. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number was not reported, Expiry date not reported) via an unspecified route of administration in Arm Left on 20Feb2021 11:00 (at the age of 38 years old) as dose 1, single for COVID-19 immunization. Patient did not receive other vaccine in four weeks of COVID vaccine. The patient experienced numbing and tingling sensation in my thumb, pointer, and middle finger of my right hand on 13Mar2021 11:45. No treatment were received for the adverse events. Outcome of the events were unknown. No follow up attempts are possible, information about lot/batch number cannot be obtained.

Other Meds: IBUPROFEN

Current Illness:

ID: 1648794
Sex: F
Age:
State: MN

Vax Date: 01/28/2021
Onset Date: 01/28/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 20210209; Test Name: Nasal Swab (antigen); Test Result: Negative

Allergies:

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

Symptoms: tingling and numbness down my right leg, into my left leg; tingling and numbness down my right leg, into my left leg/tingling sensation in my right lateral thigh; weakness in both legs from back of the buttocks into hamstrings; nerve pain down the back of my hamstrings; This is a spontaneous report from a contactable Other HCP (nurse reported for herself). A 54-year-old non-pregnant female patient received bnt162b2 (BNT162B2, Formulation: solution for injection, Lot Number: EL9262), dose 2 via an unspecified route of administration, administered in Arm Right on 28Jan2021 11:00 AM (at the age of 54-year-old) as dose 2, single for covid-19 immunisation. The patient was not pregnant at the time of vaccination. The patient other medical history was none. The patient had no Known allergies. The patient did not have COVID prior vaccination. Concomitant medication(s) included Estradiol (ESTROGEN) and Progesterone (PROGESTERONE), all taken for an unspecified indication, start and stop date were not reported. The patient previously received her first dose of bnt162b2 (BNT162B2, Formulation: solution for injection, Lot Number: EL01470), via an unspecified route of administration, administered in Left arm on 07Jan2021 11:00 AM, as single for covid-19 immunisation and about 1 1/2 weeks after the first dose of the COVID vaccine, she had a numb/tingly tingling down her right leg into the foot. No other vaccine in four weeks. On 28Jan2021, within several minutes after receiving the 2nd dose of the COVID vaccine, the patient experienced tingling and numbness down her right leg, into her left leg/tingling sensation in her right lateral thigh, weakness in both legs from back of the buttocks into hamstrings and nerve pain down the back of her hamstrings. The clinical details of the events as follows: Within several minutes after receiving the 2nd dose of the COVID vaccine, she had a rush of tingling and numbness down her right leg, into her left leg and weakness in both legs from back of the buttocks into hamstrings which was lasting about 1 1/2 weeks after the vaccine. She had nerve pain down the back of her hamstrings for about 1 1/2 weeks. It was reported that she had to be seen by a neurologist and have an MRI the days following. She had been referred to a spine Dr. to discuss the findings, but she has to get workman comp approval before she can make this appointment. She continued to have a tingling sensation in her right lateral thigh. The sensations in her buttocks, hamstrings and left leg had resolved. The events resulted in Doctor or other healthcare professional office/clinic visit. No treatment was received to treat the events. The patient underwent lab tests and procedures which included antigen test (Nasal Swab) was negative on 09Feb2021. The patient outcome of the events was Resolved with Sequel (resolved with lasting effects). No follow-up attempts are possible. No further information is expected.

Other Meds: ESTROGEN; PROGESTERONE

Current Illness:

ID: 1648795
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
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: Experiencing some numbness; This is a spontaneous report from a contactable consumer (patient) received via an automated system. This automated system responded via telephonic activity. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, 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. The patient medical and concomitant medication history were reported. The patient experienced experiencing some numbness and was not sure if patient should call Pfizer, or go to Doctor. Patient received the vaccine and was experiencing symptoms that patient had not heard about and was not sure if patient should go to the doctor or call Pfizer. Patient stated that he has been having numbness. The outcome of the event was unknown. Information on Lot/Batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1648796
Sex: F
Age:
State:

Vax Date: 03/08/2021
Onset Date: 03/01/2021
Rec V Date: 08/28/2021
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: Face numbed up on the left side; All her joints on the left side from her knee all the way to her neck bothered her; This is a spontaneous report from a contactable consumer. This consumer reported for a patient (daughter) of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number and expiration date were not reported) via an unspecified route of administration on 08Mar2021 as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that, the reporter was calling in regard for daughter, she had a reaction, reporter was just helping her out to try and find all these things to get the information. She had the Pfizer, and approximately on unknown date in Mar2021, she got a side effect of her like her face numbed up on the left side and then all her joints on the left side from her knee all the way to her neck bothered her. She was getting better now, they took the BENADRYL, and she took like Ibuprofen, but the problem they were having was they could not get any answers from doctors or anything, did she go for the second shot, or will this cause more of a serious condition with the face of numbing; asked by reporter. Reporter was trying to get information for daughter. Reporter stated, daughter will take care of herself. Reporter wanted to try and find out where she can call, as she wants to call that number and that was about it, because this was going to be frustrating for her. Outcome of both the events was recovering at the time of reporting. No follow up attempts are possible. Information about Lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1648797
Sex: F
Age:
State: CA

Vax Date: 03/02/2021
Onset Date: 03/02/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 20210302; Test Name: Heart rate; Result Unstructured Data: Test Result:Rapid

Allergies:

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

Symptoms: Rapid heart rate that hasn't stopped; Chills; Fever; body aches for 5 days; Swallen lymph node under left arm pit for 5 days and still there; This is a spontaneous report from a non-contactable consumer. This 32-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Lot number and expiry date was not reported) via an unspecified route of administration at arm Left on 02Mar2021 12:30 (at the age of 32-years-old) as a single dose for covid-19 immunisation. Medical history included thyroid disorder. Patient did not have known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. In two weeks, Other medications used Birth control and thyroid medicine. Historical vaccine BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection) dose 1 (Lot number and expiry date was not reported) via unspecified route of administration at Left arm on 09Feb2021 12:00 PM as a single dose for covid-19 immunisation. On 02Mar2021 16:30 the patient experienced rapid heart rate that hasn't stopped, chills, fever, body aches, swollen lymph node under left arm pit for 5 days and still there. The patient underwent lab tests and procedures which included heart rate: rapid on 02Mar2021. Treatment was not given for adverse events. Outcome of the events was recovered with Sequel on unspecified date in 2021 No follow-up attempts are possible; information about lot/batch number cannot been obtained

Other Meds:

Current Illness:

ID: 1648798
Sex: M
Age:
State:

Vax Date: 03/11/2021
Onset Date: 03/11/2021
Rec V Date: 08/28/2021
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: Extreme heartburn; sinus pressure with headache; sinus pressure with headache; body aches; loose bowels; fatigue.; This is a spontaneous report from a Non-contactable consumer. This consumer reported for male patient that a 45-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number: Unknown), via an unspecified route of administration on 11Mar2021 (at the age of 45 years old) as single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection) for covid-19 immunisation. The patient did not receive any other vaccines within four weeks. It was unknown that the patient had covid prior vaccination. It was unknown that the patient had tested for COVID-19 since having the vaccine. On 11Mar2021, patient experienced extreme heartburn, sinus pressure with headache, body aches, loose bowels, fatigue. It was unknown that the patient had received any treatment for events. The outcome of events was recovered on an unspecified date in Mar2021. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1648799
Sex: F
Age:
State: MS

Vax Date: 03/09/2021
Onset Date: 03/13/2021
Rec V Date: 08/28/2021
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: I awoke with a terrible headache and vomited for several hours.; vomited for several hours; I was dizzy; unable to eat with a lingering headache all weekend; This is a spontaneous report from a contactable consumer, the patient. A 39-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN), dose 1 via an unspecified route of administration, administered in Arm Left on 09Mar2021 16:30 (at the age of 39-years-old) as a single dose for covid-19 immunization. Medical history included asthma, hypertension, hypersensitivity, allergies with aspirin, burlap. Concomitant medication(s) in two weeks included mefenamic acid (ADVIL [MEFENAMIC ACID]). The patient had no other vaccine within four weeks. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 13Mar2021, Saturday, 4 days after vaccination, the patient awoke with a terrible headache and vomited for several hours. She was dizzy, unable to eat with a lingering headache all weekend. The patient did not receive any treatment. Outcome of the event was recovered on Mar2021, at the time of this report. No follow-up attempt are possible. Information about lot/batch number cannot be obtained.

Other Meds: ADVIL [MEFENAMIC ACID]

Current Illness:

ID: 1648800
Sex: F
Age:
State: OK

Vax Date: 03/08/2021
Onset Date:
Rec V Date: 08/28/2021
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: Unable to eat; very tired; unable to get out; feeling so bad; Sleeping a lot; Aching; very weak; This is a spontaneous report from a contactable consumer or other non hcp. A elderly female patient received bnt162b2 (BNT162B2 Solution for solution), via an unspecified route of administration on 08Mar2021 12:30 (Batch/Lot Number: EL9264) as SINGLE DOSE for covid-19 immunisation. Medical history included diabetes mellitus from an unknown date and unknown if ongoing , drug hypersensitivity from an unknown date and unknown if ongoing. Concomitant medication included clindamycin taken for an unspecified indication, start and stop date were not reported; meloxicam taken for an unspecified indication, start and stop date were not reported; metformin hcl taken for an unspecified indication, start and stop date were not reported. The patient experienced unable to eat, very tired, unable to get out, feeling so bad, sleeping a lot, aching and very weak. The not received any treatment for the events. The outcome of the events was resolved. No follow-up attempts are possible. No further information is expected.

Other Meds: CLINDAMYCIN; MELOXICAM; METFORMIN HCL

Current Illness:

ID: 1648801
Sex: F
Age:
State: FL

Vax Date: 02/01/2021
Onset Date: 03/01/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 202103; Test Name: Pyrexia; Result Unstructured Data: Test Result:99-103.5 Fahrenheit; Test Date: 20210312; Test Name: Covid test; Test Result: Negative ; Comments: Nasal swab

Allergies:

Symptom List: Nausea

Symptoms: nausea; vomiting; extreme fatigue; aches; fever; diarrhea; extremely painful muscle aches; malaise; This is a spontaneous report received from a contactable other healthcare professional (patient). A 56-years-old nonpregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EN6200) intramuscular, administered in Arm Left in Feb2021 14:30 (age at vaccination 56-years-old) as single dose for COVID-19 immunisation. Medical history included hypothyroid. Concomitant medication(s) included levothyroxine, multivitamin [vitamins nos], famotidine (PEPCID AC), all taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient had no allergies to medications, food, or other products. Exactly 7 days after vaccine, in Mar2021 the patient developed nausea/vomiting, extreme fatigue, aches. Lasted 4 days then started feeling better. 3 days later got fever, nausea, some vomiting & diarrhea, extremely painful muscle aches, fatigue, malaise. The patient had these symptoms for 7 days now and still with fever 99-103.5 fahrenheit.The symptoms come in waves, different from any other flu symptoms she had ever had & feel extreme. AE resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. The patient did not receive any treatment for the events. The reporter assessed the events as non-serious. Since the vaccination, the patient had been tested for COVID-19. The patient underwent covid test type post vaccination: Nasal Swab on 12Mar2021 which was negative. Outcome of the events was not recovered. Follow-up attempts completed. No further information expected.

Other Meds: LEVOTHYROXINE; MULTIVITAMIN [VITAMINS NOS]; PEPCID AC

Current Illness:

ID: 1648802
Sex: F
Age:
State: AZ

Vax Date: 03/05/2021
Onset Date: 03/05/2021
Rec V Date: 08/28/2021
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: heart rate; Result Unstructured Data: Test Result:rapid heart rate of 91; Comments: rapid heart rate of 91 two hours after receiving 1st dose of vaccine

Allergies:

Symptom List: Injection site pain

Symptoms: Rapid heart rate of 91 two hours after receiving 1st dose of vaccine.; This is a spontaneous report from a contactable consumer (Patient) or other non-healthcare professional. A 70-year-old non-pregnant female patient received bnt162b2 (FIZER-BIONTECH COVID-19 VACCINE, Batch/Lot number and Expiration date was not reported), via an unspecified route of administration, in Right Arm on 05Mar2021 at 11:00 (at the age of 70-year-old) as DOSE1, SINGLE for covid-19 immunisation. The patient medical history included drug hypersensitivity (Known allergies: Sulfa), high blood pressure and renal cancer stage iii (Verbatim: 3rd Stage Kidney Disease). The patient concomitant medications were not reported. The patient was not diagnosed with covid-19, prior vaccination and the patient had not been tested covid-19, post vaccination. The patient did not receive other vaccines within four weeks and did not receive other medications in two weeks of vaccination. On 05Mar2021 at11:00, the patient experienced rapid heart rate of 91 two hours after receiving 1st dose of vaccine. The Patient taken 5 mg Bystolic (a beta blocker) as a treatment. Therapeutic measures were taken as a result of rapid heart rate of 91 two hours after receiving 1st dose of vaccine. The adverse event resulted in doctor or other healthcare professional office/clinic visit. The outcome of the event was recovered on an unspecified date. No follow up attempts are possible. Information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1648803
Sex: F
Age:
State: FL

Vax Date: 02/27/2021
Onset Date:
Rec V Date: 08/28/2021
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: I got a little ache and pain in my left knee area; She was very agitated; This is a spontaneous report from a non-contactable consumer (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number and expiration date was not reported) via an unspecified route of administration on 27Feb2021 as dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient got a little ache and pain in her left knee area and she was very agitated on an unspecified date. It was reported that, patient was due for her 2nd shot on 22Mar2021 and she did not know what to do. Reported seriousness was non-serious. She did not know which COVID vaccine she received. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1648804
Sex: F
Age:
State: IL

Vax Date: 03/14/2021
Onset Date: 03/15/2021
Rec V Date: 08/28/2021
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 sporadically all over her body/it was on her foot, then shoulder, then knee, then back, then face/It was like spot itch; rash with welts on her chest; The caller arm is sore; rash with welts on her chest; This is a spontaneous report from a contactable consumer (patient) via medical information team. A 64-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: unknown) dose 2, via an unspecified route of administration on 14Mar2021 as single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. She received the 2nd dose of the Pfizer covid vaccine 14Mar2021 (yesterday.) On 15Mar2021, she woke up in the middle of the night with itching sporadically all over her body, but not at the same time. At one point it was on her foot, then shoulder, then knee, then back, then face. She was still experiencing that. It was like spot itch. One time the itch was in-between the toes, then on her face, then on her stomach, it kept changing all over her body. She now has a rash with welts on her chest. Her arm was sore. She wanted to know if she can take Benadryl. The outcome of events was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1648805
Sex: F
Age:
State: TX

Vax Date: 03/08/2021
Onset Date: 03/08/2021
Rec V Date: 08/28/2021
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: numbness in one cheek; tingling in head; ill feeling; cold hands; This is a spontaneous report from a contactable consumer (patient). A 47-years-old female non-pregnant patient received first dose bnt162b2 (PFIZER-BIONTEC COVID-19 VACCINE, Solution for injection, Lot Number: not reported) via unspecified route of administration in right arm on 08Mar2021 at 16:00 (at age of 47-years-old) as a single dose for COVID-19 immunisation. Medical history included migraines, fibromyalgia and cervical fusion. Concomitant and other medications in two weeks included lansoprazole (PREVACID) and clonazepam. No other vaccine in four weeks. Past drug events included allergy due to sumatriptan succinate (IMITREX), paroxetine hydrochloride (PAXIL), buspirone hydrochloride (BUSPAR) and dairy. No other vaccine received in four weeks. Patient has not been tested for COVID, post vaccination. Patient has not been tested for COVID, since the vaccination. On 08Mar2021 at 17:00 (1 hour after vaccination), patient experienced tingling in head, numbness in one cheek, cold hands and ill feeling. Events resulted in visit to doctor or other healthcare professional office/clinic. Treatment received was unknown. The outcome of all events was not resolved. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: PREVACID; CLONAZEPAM

Current Illness:

ID: 1648806
Sex: F
Age:
State:

Vax Date: 03/04/2021
Onset Date: 03/01/2021
Rec V Date: 08/28/2021
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: chills; runny nose; bones kind of ached; tiredness; headache; muscle pain; joint pain; feeling unwell; swollen lymph nodes in my neck; This is a spontaneous report from a contactable consumer (patient). A 70-year-old female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; Lot Number: was not reported), via an unspecified route of administration on 04Mar2021 (age at the time of vaccination 70-years-old) as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date Mar2021, the patient experienced chills, runny nose, bones kind of ached, tiredness, headache, muscle pain, joint pain, feeling unwell, and swollen lymph nodes in my neck. The outcome for all the events was unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1648807
Sex: F
Age:
State:

Vax Date: 01/17/2021
Onset Date:
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: not able to mobilize; developed sores in her mouth; She can't eat; This is a spontaneous report from Pfizer. A contactable consumer reported for a female patient(mother) that. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported, Expiration date: Not reported), via an unspecified route of administration on 17Jan2021 as DOSE 1 SINGLE for covid-19 immunization. The patient medical history and concomitant medication was not reported. she reports that her mom is not having a good quality of life, her mom is not able to mobilize on an unspecified date. she does not know what to do. she reports that the HCPs they have seen don't know how to resolve symptom or fix it. she reports she is aware of a similar situation that happened to a person. she does not know how to handle this; she is looking for some assistance on what to do for her mom. she would like me to email or get a hold to someone to get research because of the vaccine that her mom received was from Pfizer, or it will be a lawsuit. she would like to speak to someone else that could give her more information. she was not satisfied with response to question above she reports that if someone doesn't follow up within 24 hours that she will go to social media. Possible duplicate AE. Upon callback, caller clarified that 40 minutes after receiving the Pfizer vaccine, her mother developed sores in her mouth. She can't eat, it hurts to speak (that's what was meant by her mother is not able to speak) and they are getting worse. They look like blisters and it's only in her mouth on an unspecified date. Her quality of life is poor. She has been to the emergency room three times and has been given antibiotics, steroids and several different things and nothing seems to work. It has been seven weeks. She thinks it is Pfizer's responsibility to come up with a way to treat this since she makes the vaccine. The seriousness criteria are Disability for the event not able to mobilize. The event outcome was Unknown Medical Information: Were any unaddressed medical questions referred or forwarded to Medical Information? No No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1648808
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
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: allergic reaction to the first dose of the vaccine; This is a spontaneous report from a contactable consumer or other non-hcp (patient herself). A 72-years-old female patient received bnt162b2 (BNT162B2, Formulation: Solution for injection, Lot number was not reported, Expiry date: Unknown) via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced allergic reaction to the first dose of the vaccine on an unspecified date and she stated she knows she cannot get the second dose. The outcome of the event was unknown. Information about batch/lot number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1648809
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
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: Asthenia, Chills, Headache, Myalgia

Symptoms: experienced joint pain 2 weeks after receiving the 2nd dose of the Pfizer-BioNTech Covid-19 Vaccine; This is a spontaneous report from a non-contactable physician (patient). A male patient of an unspecified age received first dose of bnt162b2 (BNT162B2 PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot number: UNKNOWN), via an unspecified route of administration on an unspecified date as dose 1, single and second dose of bnt162b2 (BNT162B2 PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot number: UNKNOWN), via an unspecified route of administration on an unspecified date as dose 2, single both the doses for COVID-19 immunisation. The medical history and concomitant medications of the patient were not reported. The Physician said he experienced joint pain 2 weeks after receiving the 2nd dose of the Pfizer-BioNTech Covid-19 Vaccine. He wanted to know if that was normal and how long the side effects usually last and also wanted to know Pfizer's recommendations on how to treat these side effects. The outcome of the event was reported as unknown. No follow-up attempts are possible. Information on Lot/Batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1648810
Sex: F
Age:
State: NY

Vax Date: 02/22/2021
Onset Date: 03/14/2021
Rec V Date: 08/28/2021
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: 2021; Test Name: Nasal test for COVID; Result Unstructured Data: Test Result:Negative; Test Date: 2021; Test Name: . She can't hold things like she wants to; Result Unstructured Data: Test Result:decreased

Allergies:

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

Symptoms: left side started to feel numb dragging of her leg/Left side is toatally intereupted; Injected limb mobility decreased; sore, injection arm; She can't hold things like she wants to; This is a spontaneous report from a contactable female consumer reported for herself. A 67-year-old female patient received bnt162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE; Solution for injection Lot number was not reported) via an unspecified route of administration in arm left on 22Feb2021 15:45 as dose 1, single at the age of 67-years-old for COVID-19 immunisation. Medical history included asthma from an unknown date and unknown if ongoing, ongoing HIV positive. Concomitant medications were not reported. It was provided for the other conditions that onset date as let's just say over 20 years but reported condition is well controlled, and her being very healthy. It is a flare up thing, not all the time. She uses an inhaler every now and then for asthma but is doing well. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available) was none. Additional Vaccines Administered on Same Date of the Pfizer Suspect: Vaccines If applicable, all vaccines administered on same date with the Pfizer vaccine considered as suspect was none. On 14Mar2021 11:30, patient experienced left side is totally interrupted. She can't hold things like she wants to, and her left foot is dragging a little bit. Affecting her left side including shoulder, arm, leg and foot. Outcome is a little worse. She cannot work like this, unable to work today and wants to work the other day. Hypoaesthesia, Injected limb mobility Injected limb mobility decreased sore, injection arm injection site pain, left side started to feel numb, dragging of her leg, minimal use of left arm. The adverse event did not result in emergency room/physician office visit. Patient was not hospitalized. It was mentioned later in the call that she was local yesterday at time of onset of event. She has not travelled out of the area in the last 3 weeks. Dose change: she was supposed to go back on 26Mar2021 for second dose but has no plan to get second dose due to this event. The patient underwent lab tests and procedures which included sars-cov-2 test negative resulted as negative on an unknown date 2021, she can't hold things like she wants to resulted as decreased on an unknown date 2021. The clinical outcome of the event left side started to feel numb dragging of her leg/Left side is totally interrupted was not resolved and rest of the events was unknown. No follow up attempts are needed. Information about lot/ batch number cannot be obtained.

Other Meds:

Current Illness: HIV positive

ID: 1648811
Sex: F
Age:
State: CT

Vax Date: 03/14/2021
Onset Date: 03/14/2021
Rec V Date: 08/28/2021
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: Extreme itching in mouth and throat 6 hours after injection; numbness; nerve pain in left ring finger then pinky and around arm pit and top of left wrist; Stiffness in jaw; This is a spontaneous report from a contactable consumer. This 59-year-old female consumer reported. A 59-year-old non-pregnant female patient (not pregnant at the time of vaccination) received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration, administered in Arm Left on 14Mar2021 14:45 (age at the time of vaccination was 59-year-old) as dose 1, single for COVID-19 immunization. Medical history included Tree nut allergy from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient did not receive any other vaccine prior to COVID-19 Vaccine. The patient did not receive any other medication prior to COVID-19 Vaccine in 2 weeks. The patient did not test COVID-19 positive prior to vaccination. The patient had not been tested for COVID-19 since the vaccination. It was reported that, on 14Mar2021, at 15:00, within 10 min of injection, numbness and nerve pain in left ring finger then pinky and around arm pit and top of left wrist. Stiffness in jaw. Extreme itching in mouth and throat 6 hours after injection on 14Mar2021 20:45. No treatment was received for the event. The outcome of the events wee recovered on an unspecified date on 2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1648812
Sex: F
Age:
State:

Vax Date: 03/14/2021
Onset Date:
Rec V Date: 08/28/2021
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: edema in my legs; swelling under my eyes; This is a spontaneous report from a contactable consumer reporting for herself. A 61-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number and Expiration date was not reported), via an unspecified route of administration on 14Mar2021 as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced edema in legs, swelling under eyes on an unspecified date. Caller stated she received her 1st Pfizer vaccine dose the day before this report on 14Mar2021 (yesterday) and had developed edema in her legs and swelling under her eyes. And asked if this was normal. The events were not serious. Clinical outcome of events was unknown. Information on lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1648813
Sex: F
Age:
State: AZ

Vax Date: 03/07/2021
Onset Date: 03/07/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies: Sulfonamide allergy

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

Symptoms: This is a spontaneous report from a contactable consumer or other non-HCP (patient). A 67-year-old (non-pregnant) female patient received unknown dose number of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, solution for injection, batch/lot# not reported), at age 67, via an unspecified route of administration, on Mar 7, 2021, at 11:15, single dose, for COVID-19 immunization. Medical history included drug hypersensitivity from an unknown date. Concomitant medication included Synthroid for an unspecified indication; start and stop date not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. The patient did not test COVID-19 positive prior to vaccination. No COVID-19 prior vaccination. The patient has not tested for COVID-19 post the vaccination. On Mar 7, 2021, at 11:15, patient experienced numbness of lower left-side of lip and left-side of face. The patient did not receive treatment for the events. The outcome of the events: recovered on an unspecified date in Mar 2021. No follow-up attempts possible. Information about batch/lot number cannot be obtained.

Other Meds: Synthroid

Current Illness:

ID: 1648814
Sex: F
Age:
State: NC

Vax Date: 01/25/2021
Onset Date: 01/26/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Date: 20210126; Test Name: Heart rate; Result Unstructured Data: Test Result:Rapid Pounding

Allergies:

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

Symptoms: Rapid Pounding Heart rate; severe stomach pain; This is a spontaneous report from a contactable consumer (patient). A 65-years-old non-pregnant female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EL3247), via an unspecified route on 25Jan2021 at 11:00 (at the age of 65-years) as dose 1, single in the left arm for covid-19 immunisation. The patient medical history included MPV, Osteoporosis and known allergic to Niacin. The patient concomitant medications included levothyroxine sodium (SYNTHROID), Atenolol, Zinc, Vitamin C, Probiotic from an unknown date and ongoing. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 26Jan2021 at 01:30, the patient experienced rapid pounding heart rate, severe stomach pain. Severe stomach pain lasted for 4 days. The patient visited to Doctor or other healthcare professional office/clinic. The patient did not received treatment for events. The patient underwent lab tests and procedures which included heart rate was rapid pounding on 26Jan2021. The outcome for the events was recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: SYNTHROID; ATENOLOL; ZINC; VIT C; PROBIOTICS

Current Illness:

ID: 1648815
Sex: F
Age:
State: LA

Vax Date: 03/10/2021
Onset Date: 03/10/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data: Test Name: BMI; Result Unstructured Data: Test Result:35.3 kg/m2; Test Date: 20210310; Test Name: heart; Result Unstructured Data: Test Result:racing

Allergies:

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

Symptoms: aching arm; rash on my bicep/plus feeling flush with rashes appearing on both arms, my chest and my face.; Arm is sore at injection site.; heart began racing; light headed/I am dizzy; I was not comfortable to drive; my injection arm began to ache from my bicep to my finger tips with sharp pains in the wrist.; rash on my bicep/plus feeling flush with rashes appearing on both arms, my chest and my face.; This is a spontaneous report from a contactable consumer (patient) reporting for herself. A 40-year-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EN6204), via an unspecified route of administration, administered in Left arm on 10Mar2021 17:30 at the age of 40-years-old as single dose for COVID-19 immunisation. Medical history included Insulin resistance, obese class II (BMI 35.3 kg/m2)) from an unspecified date. Concomitant medications included phentermine hydrochloride, topiramate (QSYMIA) taken for an unspecified indication, citalopram hydrobromide (CELEXA) taken for an unspecified indication, buprenorphine hydrochloride, naloxone hydrochloride (SUBOXONE) taken for an unspecified indication, metformin taken for an unspecified indication, omeprazole taken for an unspecified indication from an unspecified date received in two weeks of vaccination. The patient previously took Sulfa and experienced allergy. The patient did not receive other vaccine in four weeks of vaccination. The patient was not diagnosed with COVID-19 prior vaccination. The patient has not been tested for COVID-19 post vaccination. Facility type vaccine was Unknown. On 10Mar2021 at 17:30, Immediately after receiving injection, the patient experienced heart began racing and she became light headed. she sat in observation for 15 mins, then was handed her card and told she could leave. she was not comfortable to drive, so she sat in her vehicle for approximately 10 additional minutes. As the night continued, her injection arm began to ache from her bicep to her fingertips, with sharp pains in the wrist. she also developed a rash on her bicep below the injection site. she took an aleve and Immediately went to bed. she does not remember falling asleep. she woke up early the next morning on 11Mar2021, with a full day of appointments, so she took an aleve to help with the aching arm. At first, it was only aching at the infection site, but as the day progressed she began to feel the se pain/aching she felt the day prior, plus feeling flush with rashes appearing on both arms, her chest and my face. It was now almost 24 hours post-injection and she was about to lay down as she was dizzy. Her arm was sore at injection site on 10Mar2021 at 17:30. ae resulted in None of the above. Treatment for ae was No. Therapeutic measures were taken as a result of my injection arm began to ache from my bicep to my fingertips with sharp pains in the wrist. (pain), rash on my bicep/plus feeling flush with rashes appearing on both arms, my chest and my face. (rash), aching arm (pain in extremity). The patient underwent lab tests and procedures which included body mass index: 35.3 kg/m2 on an unspecified date, heart rate: racing on 10Mar2021. The outcome of events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: QSYMIA; CELEXA [CITALOPRAM HYDROBROMIDE]; SUBOXONE; METFORMIN; OMEPRAZOLE

Current Illness:

ID: 1648816
Sex: F
Age:
State: WA

Vax Date: 03/10/2021
Onset Date: 03/11/2021
Rec V Date: 08/28/2021
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: numbness in left hand, especially thumb; This is a spontaneous report from a non-contactable consumer or other non hcp (patient reported for self). A 35-years-old (non pregnant) female patient received first dose of BNT162bB (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number: UNKNOWN), via an unspecified route of administration, administered in Left arm on 10Mar2021 16:45 (at the age of 35-years-old) as dose 1, single for COVID-19 immunisation. (Lot unknown reason: Unable to locate or read the details). Medical history included known allergies to Penicillin. There were no concomitant medications, no other medications in two weeks. No other vaccines were received in four weeks. The patient was not diagnosed with COVID-19 prior to the vaccination. On 11Mar2021 08:00, the patient experienced numbness in left hand, especially thumb. Patient has not been tested for COVID-19 since the vaccination. No treatment was received for the adverse event. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1648817
Sex: F
Age:
State: TX

Vax Date: 03/10/2021
Onset Date: 03/10/2021
Rec V Date: 08/28/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: I am breastfeeding mom; I am breastfeeding mom; sore arm; This is a spontaneous report from a contactable other HCP (Patient). This other HCP reported for two patients (mother and baby). This report is for mother. A 39-years-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID VACCINE; Solution for injection) via an unspecified route of administration, administered in left arm on 10Mar2021 14:15 (Batch/Lot Number: EN6199) as DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history and patient's concomitant medications were not reported. No known allergies reported. The patient stated that I am breastfeeding mom, I (myself) didn't have any other reaction other than a sore arm on 10Mar2021 17:30. There were no other vaccine in four weeks and there were no other medications in two weeks. Patient did not have COVID prior vaccination and also patient was not COVID tested post vaccination. Treatment was not received for any AE. The outcome of event was recovered. No follow-up attempts are possible. No further information is expected. ; Sender's Comments: Linked Report(s) : PFIZER INC-2021287948 Mother/Baby case

Other Meds:

Current Illness:

ID: 1648818
Sex: M
Age:
State: TX

Vax Date: 03/10/2021
Onset Date: 03/10/2021
Rec V Date: 08/28/2021
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: Test Name: temperature; Result Unstructured Data: Test Result:99.6 Fahrenheit; Comments: went up

Allergies:

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

Symptoms: Breastfeeding mom/nursed him multiple times right after I vaccinated; Had 99.6 F temperature/temperature went up/fever; Diarrhea; This is a spontaneous report form a contactable other Health Care Professional (mother). A 19-month-old male patient received BNT162B2 (COMIRANTY; Formulation: Solution for injection; Lot number: En6199, Expiration date: was not reported) via transmammary on 10Mar2021 as dose 1, single for COVID-19 immunization. Medical history and concomitant medications were not reported. On 10Mar2021 18:15, reporter stated her son was 19 months old. He had 99.6 F temperature and diarrhea 4 hrs after she got vaccinated (I nursed him multiple times right after I vaccinated and when his temperature went up). She also stated I am breastfeeding mom. It looks like it was transitory as this morning he no longer had a fever. He was not sick from anything else as he was in good health prior to me vaccinated and he didn't present any other symptoms. I believe the vaccine made his body react (for a brief period of time). The patient mother was not diagnosed with COVID prior vaccination and was not tested post vaccination. The outcome of event fever was recovered while other events were unknown. Follow-up (11Jun2021): Follow-up attempts completed. No further information expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021287049 Mother/Baby case

Other Meds:

Current Illness:

ID: 1648819
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 08/28/2021
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: nerve numbness on left face, abdomen, lower leg and calf numbness; This is a spontaneous report from a contactable consumer or other non hcp. This report was received via a sales representative. A 53-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Lot number and expiration dates were not reported), dose 1 via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient developed nerve numbness on left face, abdomen, lower leg and calf numbness in 3 hours of receiving the vaccine. He was afraid to receive the second dose due to the side effects. The reporter reported that regret involving case in this inquiry. Reporter felt like it may muddy the waters. So please de-emphasize reporter's personal involvement & perspective in this matter. 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: 1648820
Sex: F
Age:
State: MS

Vax Date: 02/10/2021
Onset Date: 02/10/2021
Rec V Date: 08/28/2021
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: swelling of her leg and cheeks; swelling of her leg and cheeks; Left Knee Swelling; Swelling on inside of Jaws; pain in her arm; Edema; swelling and pain at the site of the shot; swelling and pain at the site of the shot; This is a spontaneous report from a contactable nurse. A 70-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/Lot Number: EN5318), dose 1 via an unspecified route of administration in arm left on 10Feb2021 at 10:10 as single dose for COVID-19 immunisation. Medical history included allergy to arthropod bite from an unknown date and unknown if ongoing specifically fire ants and spiders. Concomitant medication included prednisone (PREDNISONE) taken for hypersensitivity, start and stop date were not reported. Caller reports that she received her first vaccine dose and 4 days later she had some symptoms of pain in her arm and Edema, with swelling of her leg and cheeks. She reports that has the same type of reaction with fire ant because she is allergic to them. She reports that she has seen her HCP who prescribed her some prednisone but he was not able to provide guidance of whether or not she should get the second dose of the vaccine. She calls today for guidance. she had a reaction like she does for insect bites, she started swelling up. She states that she took Benadryl on Wednesday 10Feb2021. She states the arm was painful and swollen and two to three days later her left leg was swollen along with the inside of her jaw was swollen. Caller states that she took some prednisone because she got scared. Caller asking if she should take the second one or wait until a third comes out if they do release that? Arm Pain and Swelling: States it lasted for 5-7 days, well actually it lasted 14 days because she had a pain now and then. Treatment: Took Prednisone 10mg med dose where she takes for ant bites, like Z-pack and you take so many one day and level off back to one. Clarifies that Benadryl was taken the first day or two, and then she saw more edema on Saturday and how bad it had gotten so she took the Prednisone since the Benadryl wasn't working. Also states that she took Tylenol because it hurt. She states that like with the insect bites, the swelling keeps on getting bigger and bigger. It starts out a little bit and then the edema spreads and her whole hands swell. States she noticed by Saturday the edema went down to her left knee. Patient was not hospitalized nor admitted to an Intensive Care Unit, no organ involvement. PSCC Communication: PC Filed. Caller provided with Report Reference. The caller was provided with the website, and the phone number for USMI, # opt. 3, and hours of operation 8:00-20:00 EST Mon-Sun, prior to cold transfer to wait in queue, due to high call volumes in USMI. Is there a Product Complaint: Yes Description of Product Complaint: Description of complaint: Calling to report adverse events from the COVID Vaccine. States that she took Benadryl for the swelling but it did not help. Lot: 1642806 Expiration: Dec20 UPC:#. Dosage: 25mg liquid gels. Outcome of the event pain in extremity, swelling and pain at the site of the shot, left knee swelling, swelling on inside of jaws was recovered on unspecified date of 2021, for the event edema, swelling of her leg and cheeks unknown Follow-up (01Jul2021): Follow-up attempts completed. No further information expected.

Other Meds: PREDNISONE

Current Illness:

ID: 1648821
Sex: M
Age:
State: AZ

Vax Date: 03/01/2021
Onset Date: 03/01/2021
Rec V Date: 08/28/2021
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: Upper respiratory issues; COPD; Asthma; Has issues now with his health, the allergies and different things now that are kicking in on him; Has issues now with his health, the allergies and different things now that are kicking in on him; This is a spontaneous report from a contactable consumer reporting for husband. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number: EN6202; Expiration date was not reported), via an unspecified route of administration on 01Mar2021 as dose 1, single for Covid-19 immunization. Medical history included chronic obstructive pulmonary disease, asthma from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient experienced upper respiratory issues, COPD, asthma, had issues with his health, the allergies and different things now that were kicking in on him on Mar2021. Reporter stated patient had his first Pfizer shot was 9 days ago. At the time of this report, he was having some issues with (incomplete sentence), he had upper respiratory issues. He was due to take his next shot, reporter thought it was on 21 or 22nd. If patient wanted to take Prednisone as an antibiotic, reporter asked if he could still get the second dose. Patient had not taken it yet. He did not know if he can, and reporter asked what would happen if he did not get the second shot. When paraphrased about the concern, reporter stated patient had COPD and asthma (further not clarified if consumer had COPD and Asthma prior taking the COVID-19 Vaccine or not, hence captured as event). Reporter added patient did not have any problem with the shot. It was just he had issues then with his health, the allergies and different things now that were kicking in on him. Reporter stated that it was not with the shot, and do not think to be. Reporter was informed about Pfizer Medical Information and telephone # was shared. Reporter was unwilling to share further information, hence, product details (NDC, UPC) and other details were unknown. Limited information was available over the call. Clinical outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am