VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 10/01/2021
** VAERS DATABASE Last updated: October 1, 2021**
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Manufacturers

Total Manufacturer

Incidents per State

State Total
72,296
AK1,638
AL5,339
AR3,412
AS44
AZ13,316
CA58,147
CO11,002
CT7,824
DC1,626
DE1,670
FL36,235
FM3
GA13,429
GU82
HI2,195
IA4,332
ID2,473
IL19,261
IN22,568
KS4,284
KY6,945
LA4,714
MA13,886
MD11,901
ME2,997
MH8
MI17,865
MN11,345
MO8,919
MP30
MS2,676
MT2,147
NC15,401
ND1,273
NE2,732
NH2,859
NJ17,232
NM3,702
NV4,071
NY32,763
OH18,072
OK5,940
OR7,954
PA22,457
PR2,104
QM2
RI1,911
SC6,055
SD1,133
TN8,691
TX34,122
UT4,023
VA13,944
VI49
VT1,661
WA13,811
WI10,395
WV2,220
WY805
XB5
XL1
XV2

ID: 0973481
Sex: M
Age:
State: VA

Vax Date: 12/18/2020
Onset Date:
Rec V Date: 01/26/2021
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Symptoms: numbness in his right hand; This is a spontaneous report from a contactable pharmacist (patient himself). A 50-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection; lot number: EH9899, expiration date was unknown), intramuscularly on the right arm on 18Dec2020 at 12:00 at a single dose for COVID-19 immunization administered at the hospital. The patient had no medical history. He had no known allergies. There were no concomitant medications. The patient had no other vaccine in four weeks and had no other medications in two weeks. The patient had no Covid prior to vaccination. He was not tested for Covid post vaccination. On an unspecified date, following the first vaccine, the patient had numbness in his right hand for two (x2) days. The patient did not receive any treatment for the event. The patient recovered from the event "numbness in his right hand" on an unspecified date.

Other Meds:

Current Illness:

ID: 0973482
Sex: F
Age:
State:

Vax Date: 01/11/2021
Onset Date:
Rec V Date: 01/26/2021
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Symptoms: side effects of sore arm; mild itching; This is a spontaneous report from a contactable consumer. A 61-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration on 11Jan2021 at a SINGLE DOSE for covid-19 immunisation. The patient's medical history was not reported. There were no concomitant medications. On an unspecified date, the patient reported side effects of sore arm and mild itching and she stated they were very mild and lasted about 72 hours. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973483
Sex: F
Age:
State: GA

Vax Date: 12/22/2020
Onset Date:
Rec V Date: 01/26/2021
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Symptoms: body ache/ all over achy feeling; muscle aches; feeling like coming down with the flu; This is a spontaneous report from a contactable healthcare professional (patient). A 58-year-old female patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number= EJ1685), via an unspecified route of administration on left arm at 11:45 AM on 22Dec2020 at single dose for COVID-19 immunization. Medical history included Graves Disease and COVID-19 (Prior to vaccination, diagnosed with COVID-19). Concomitant medication included ibuprofen (MOTRIN), diclofenac sodium. The patient previously took percocet and experienced allergies, darvocet and experienced allergies. The patient experienced body ache and muscle aches the day after first shot also feeling like coming down with the flu all over achy feeling on unknown date that resolved in a days time. Since the vaccination, the patient had not been tested for COVID-19. The outcome of events was recovered on unknown date.

Other Meds: Motrin [Ibuprofen]; Diclofenac Sodium

Current Illness:

ID: 0973484
Sex: F
Age:
State: IN

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 01/26/2021
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Symptoms: welts all over (her) body; Itching; Red welts all over body; This is a spontaneous report from a contactable consumer. An 80-year-old female consumer BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL3248) on 13Jan2021 at 12:00 p:m at single dose for COVID-19 immunization. Relevant medical history included penicillin and bee stings allergies. Concomitant medications were not reported. On 13Jan2021, about 3 hours after vaccine patient experienced red welts were all over her body, face, arms, and under breasts. She was itching all over. Patient took three allergy pills and the reaction subsided. Patient didn't provide product name of allergy pills. Patient informed she had a reaction before to Penicillin and clarified her reaction with Penicillin was red welts and itching, but her tongue didn't get sick on an unspecified date. Patient was supposed to go back and get second COVID-19 Vaccine, but she was not going to take it unless there is a COVID-19 Vaccine without Penicillin in it (as reported). Provided date on patient card of 03Feb2021. At the time of the reporting event outcome was unknown.

Other Meds:

Current Illness:

ID: 0973485
Sex: F
Age:
State: NC

Vax Date: 01/08/2021
Onset Date: 01/01/2021
Rec V Date: 01/26/2021
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Symptoms: weakness/feeling weak; Dizziness/head was dizzy; nausea; Neck was sore; discomfort; This is a spontaneous report from a contactable consumer (patient). An 81-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: EK9231, Expiry Date: Apr2021), via an unspecified route of administration at right arm on 08Jan2021 13:00 at single dose for covid-19 immunization. Vaccine was not administered at military facility. Vaccination facility type was health department. The patient got the flu shot every year and never had a problem. There were no concomitant medications. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 13Jan2021, the patient experienced severe dizziness/head was dizzy, feeling weak, nausea, neck was sore. The events did not require a visit to emergency room or physician office. She was very dizzy and laid back down. Today (14Jan2021) was better but she felt weak and wanted to figure out what was going on. She took it to make sure she felt better but the only thing she's had was discomfort. No treatment, not contacted the doctor. The outcome of events weakness/feeling weak, dizziness/head was dizzy was recovering. The outcome of events nausea, neck pain was not recovered. The outcome of event discomfort was unknown.

Other Meds:

Current Illness:

ID: 0973486
Sex: F
Age:
State:

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 01/26/2021
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Symptoms: Rash on stomach; itching all over body; This is a spontaneous report from a non-contactable other healthcare professional (HCP). A 37-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: El3302), intramuscular at right arm on 14Jan2021 11:30 at single dose for covid-19 immunization. The COVID-19 vaccine was administered at Hospital. Medical history included granulomatous mastitis and allergy to Shrimp. The patient's concomitant medications was reported as none (no other medications in two weeks). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced rash on stomach and itching all over body on 14Jan2021 11:45. Treatment received included Allegra. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was recovering. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 0973487
Sex: F
Age:
State: GA

Vax Date: 01/13/2021
Onset Date: 01/14/2021
Rec V Date: 01/26/2021
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Symptoms: Severe muscle and joint pain.; Severe muscle and joint pain.; Stiffening is joints; This is a spontaneous report from a contactable other healthcare professional. A 47-year-old female patient received second dose of dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date: unknown) intramuscular in the right arm, on 13Jan2021 at 14:15 at a single dose, for COVID-19 immunization. Medical history included depression. Concomitant medications included escitalopram oxalate (LEXAPRO). The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: expiry date: unknown) on 22Dec2020, at 09:30 AM in the right arm for COVID-19 immunization. The patient is not pregnant at the time of vaccination. The patient was not diagnosed with COVID prior vaccination. The patient did not receive other vaccines within four weeks prior to COVID vaccination. The vaccine was administered in the hospital. On 14Jan2021 at 05:15 A.M., the patient experienced severe muscle and joint pain, and stiffening of joints. The patient did not receive treatment for the events. Outcome of the events was not recovered. The patient has not been tested for COVID-19 since vaccination. Information of lot/batch number has been requested.

Other Meds: LEXAPRO

Current Illness:

ID: 0973488
Sex: M
Age:
State: MA

Vax Date: 01/06/2021
Onset Date: 01/13/2021
Rec V Date: 01/26/2021
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Symptoms: Numbness in the right thigh anterior and lateral aspects; This is a spontaneous report from a contactable physician (patient). This 53-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) 2nd dose (lot number:EJ1686) 06Jan2021 01:00 PM at left arm at single dose intramuscular for Covid-19 immunization. Facility type vaccine was hospital. Medical history was reported as "none". Patient had no known allergies. Concomitant drug in two weeks included finasteride (PROPECIA), acetylsalicylic acid (ASPRIN), atorvastatin, and multivitamin. Patient received 1st dose of BNT162B2 (lot number: EK5730) on 17Dec2020 01:30 PM at right arm for Covid-19 immunization. No other vaccine received in four weeks. It was unknown if covid prior vaccination. No covid tested post vaccination. Patient experienced numbness in the right thigh anterior and lateral aspects on 13Jan2021 starting on 09:00 PM. No treatment received. Outcome of the events was not resolved.

Other Meds: PROPECIA; ASPRIN; ATORVASTATIN

Current Illness:

ID: 0973489
Sex: F
Age:
State: NY

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
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Symptoms: Fever on evening of second vaccine - highest was 100 - Fever between 98-99.6; Body aches throughout body Headache; Body aches throughout body Headache; Chills; This is a spontaneous report from a contactable Other HCP. This 56-year-old female Other HCP (patient) reported for herself that she received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot unknown: EL3246), via intramuscular at left arm on 12Jan2021 09:30AM at single dose for COVID-19 immunization. Medical history included known allergies: penicillin. Concomitant drugs included ascorbic acid (VITAMIN C). Historical vaccine included the first dose of BNT162B2 (Lot number: EH9899) on 22Dec2020 10:30AM via intramuscular at left arm for COVID-19 immunization. No other vaccine in four weeks. No COVID prior vaccination. No COVID tested post vaccination. On 12Jan2021 08:00pm, patient had fever on evening of second vaccine -highest was 100 -Fever between 98-99.6 next day and evening, body aches throughout body, headache, chills, fever gone after 40 hours or so. No treatment for AE. Outcome of events was recovered in Jan2021.

Other Meds: VITAMIN C [ASCORBIC ACID]

Current Illness:

ID: 0973490
Sex: F
Age:
State: WI

Vax Date: 01/07/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
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Symptoms: Right arm numbness; Right arm numbness and discomfort when raising at shoulder level and above; This is a spontaneous report from a contactable nurse (patient). A 55-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL1284), intramuscularly on 07Jan2021 08:15 at right arm, at single dose for covid-19 immunization. The patient medical history was not reported. Concomitant medication included omeprazole, potassium gluconate; oenothera biennis oil (EVENING PRIMROSE); ascorbic acid (VIT C); glucosamine; ascorbic acid, biotin, calcium pantothenate, cyanocobalamin, folic acid, nicotinic acid, pyridoxine hydrochloride, riboflavin, thiamine hydrochloride, tocopheryl acetate (MULTIVITAMIN). The patient previously took clarithromycin (MACROBID) and known allergies was Macrobid. The patient was not pregnant at the time of vaccination. The patient experienced right arm numbness and discomfort when raising at shoulder level and above on 12Jan2021. No treatment was received. The outcome of the events was not recovered. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine.

Other Meds: Omeprazole; Potassium Gluconate; Evening Primrose; Vit C; Glucosamine; Multivitamin [Ascorbic Acid; Biotin; Calcium Pantothenate; Cyanocobalamin; Folic Acid; Nicotinic Acid; Pyr

Current Illness:

ID: 0973491
Sex: M
Age:
State: GA

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 01/26/2021
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Symptoms: Sore muscles; Slight headaches; This is a spontaneous report from a contactable consumer (patient). A 50-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EK9231; Expiration date was not reported) on 13Jan2021 (13:30) at a single dose on the left arm, with route of administration unspecified for COVID-19 immunization at the workplace clinic. Medical history included high blood pressure (HBP); and high cholesterol. Concomitant medications included atorvastatin, citalopram, metoprolol and fenofibrate. The patient previously took dextromethorphan, and had drug allergy. On 13Jan2021 (15:00), the patient had sore muscles and slight headaches. The patient had not received any treatment for the reported events. The outcome of the events, sore muscles and slight headaches, was recovered in Jan2021. The patient was not diagnosed with COVID-19 prior to vaccination, and had not been tested post-vaccination. No follow-up attempts are possible. No further information is expected.

Other Meds: Atorvastatin; Citalopram; Metoprolol; Fenofibrate

Current Illness:

ID: 0973492
Sex: F
Age:
State: NY

Vax Date:
Onset Date:
Rec V Date: 01/26/2021
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Symptoms: Tested positive after 7 days of taking the vaccine; Tested positive after 7 days of taking the vaccine; This is a spontaneous report from a contactable Pharmacist. A female patient of unknown age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, on an unknown date at single dose for COVID-19 immunisation. Medical history and concomitant medications were unknown. The patient tested positive after 7 days of taking the vaccine. Patient also received the "Bam antibodies", monoclonal antibody. Outcome was unknown. Information on the lot/batch number has been requested.; Sender's Comments: The association between the event lack of effect (tested positive) with BNT162b2 can not be completely excluded.

Other Meds:

Current Illness:

ID: 0973493
Sex: F
Age:
State:

Vax Date: 01/11/2021
Onset Date: 01/01/2021
Rec V Date: 01/26/2021
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Symptoms: feeling achy; headache; chills; This is a spontaneous report from a contactable consumer (patient). A 60-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not specified), via an unspecified route of administration on 11Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient got the first shot of the COVID vaccine on 11Jan2021. She was still feeling achy, headache and chills on an unspecified date in Jan2021, and she was working on it, but she would like to know how long will this side effects last. The outcome of the events was not recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973494
Sex: F
Age:
State: NC

Vax Date: 12/17/2020
Onset Date:
Rec V Date: 01/26/2021
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Symptoms: Ringing in ears; This is a spontaneous report from a contactable nurse (patient). A 39-year-old female patient received bnt162b2, via an unspecified route of administration in left arm on 17Dec2020 16:00 (first dose, lot number: EJ1685, expire: unknown) at single dose, via an unspecified route of administration in left arm on 08Jan2021 09:00 (second dose, lot number: EL3246, expire: Apr2021) at single dose for COVID-19 immunization. Medical history included very frequent yeast infections that started about eight years ago, hypothyroidism from an unknown date and unknown if ongoing (she has been on medication her whole life). Concomitant medication included thyroid (ARMOUR THYROID) at 90 mg daily for hyperthyroidism (she has been on this particular medication about a year, but she has been on thyroid medication her whole life). The patient experienced ringing in ears on an unspecified date. She got two doses of Pfizer vaccine. It may be a coincidence. She started having intermittent ringing in ears and now it had been constant for 3 or 4 days in a row. She had continuous ringing in her ear and has never had problems with her ears before. It wasn't going away. She was at the point to go to the doctor. She honestly didn't know the date. She noticed it intermittently about the time she got the COVID vaccine. She didn't really pay much attention. She got the second shot about the time it started constantly. She couldn't say 100%, maybe it was coincidental. Caller clarified that she noticed intermittent ringing in the ears about the same time of the first dose. She noticed constant ringing about the same time as the second dose. She would rate seriousness criteria at a five, in the middle. It is not requiring hospitalization, but she would seek medical treatment if it didn't go away. The outcome of event was not resolved. Vaccination facility type was hospital. No additional vaccines administered on same date of the Pfizer suspect. The events were not required a visit to emergency room nor physician office at this time, but she was considering seeing her doctor or an ENT. No AE following prior vaccinations. No relevant tests.

Other Meds: ARMOUR THYROID

Current Illness:

ID: 0973495
Sex: F
Age:
State: MN

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
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Symptoms: had fever max 100.8; chills; severe body aches; headaches; weakness; fatigue; This is a spontaneous report from a contactable other hcp (patient) reported that a 52-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK 4176), via an unspecified route of administration on the left arm on 12Jan2021 13:15 at a single dose for covid-19 immunisation. Medical history included PCN allergy from an unknown date. Prior to vaccination, the patient was not diagnosed with COVID-19. Patient was not pregnant at the time of vaccination. Concomitant medications included multivitamins, vitamin d [vitamin d nos] (VITAMIN D [VITAMIN D NOS]) and fish oil (FISH OIL). The patient previously received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ 1685) on 22Dec2020 13:00 on the left arm for covid-19 immunization and stated that had no issues after first vaccination. On 12Jan2021 21:00, the patient had fever max 100.8 (no unit reported), chills, severe body aches, headaches, weakness, and fatigue. The patient underwent lab tests and procedures which included body temperature: max 100.8 (no unit reported) on 12Jan2021 21:00. As treatment, patient received OTC NSAIDS. The outcome of the events was recovered. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds: VITAMIN D [VITAMIN D NOS]; FISH OIL

Current Illness:

ID: 0973496
Sex: F
Age:
State: MI

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
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Symptoms: arm was extremely sore; injection was in the right arm, about 6 hours later of the vaccination, there was mild tenderness; This is a spontaneous report from a contactable consumer. A 68-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL3248), via an unspecified route of administration in right arm on 12Jan2021 03:45 at a single dose for covid-19 immunization. Medical history included fibromyalgia, and allergies to Flexeril, benzalkomium chloride, iodoprophnyl butylcarbamate, Neosporin. Concomitant medication included prednisolone, cetirizine hydrochloride (ZYRTEC [CETIRIZINE HYDROCHLORIDE]), magnesium, cobamamide (VITAMIN B12 [COBAMAMIDE]), vitamin c [ascorbic acid] (VITAMIN C [ASCORBIC ACID]) and colecalciferol (VITAMIN D [COLECALCIFEROL]). The injection was in the right arm, about 6 hours later of the vaccination, on 12Jan2021, 22:00, there was mild tenderness. The following day, on 13Jan2021, the arm was extremely sore. 36 hours after the injection, the arm was no longer sore. The outcome of the events was recovered on 14Jan2021. No treatment was received for the events. The events were assessed as non-serious. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient was not tested for COVID-19.

Other Meds: Prednisolone; Zyrtec [Cetirizine Hydrochloride]; Magnesium; Vitamin B12 [Cobamamide]; Vitamin C [Ascorbic Acid]

Current Illness:

ID: 0973497
Sex: F
Age:
State:

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
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Symptoms: Heated nerve sensation / from the deltoid to shoulder to neck she started to have a nerve sensation; This is a spontaneous report from a contactable other healthcare professional (HCP, patient). A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 11Jan2021 at single dose for COVID-19 immunization. Medical history and concomitant medication were not reported. Patient received Pfizer COVID-19 Vaccine yesterday, 11Jan2021. After vaccine was given, the administrator rubbed the site for at least 10 seconds very hard in a back and forth motion (The person that gave her the injection applied pressure and rubbed her arm very hard, She didn't see anyone else doing it like that on tv.). When waiting for the 10 minutes, caller noticed a nerve sensation going from the deltoid to the shoulder and to her neck. When she turned her head to that side, the sensation exacerbated. After 10 minutes it did dissipate. When she used the left arm she noticed the nerve sensation (She has been using her left arm quite a bit and has been having the nerve sensation, It is not unbearable, but she noticed it in the lower part of the arm). Patient wanted to know if the administrator was supposed to rub the injection site. Wants to know if the nerve sensation was due to the administration or the vaccine (According to the other person this doesn't sound like a normal thing with the vaccine. She is hoping she didn't hit a nerve). Did notice the nerve sensation was more like in the lower arm today and it was not as strong as it was yesterday. Stated the sensation was felt like a heated nerve sensation. Stated if USMI determines it's an issue with the COVID-19 Vaccine then she will allow for follow up. She would hate to relate it to the vaccine when it could be a simple thing. Does not want to deter people from getting the vaccine. The other agent she spoke to said out of 40,000 injections nobody had that issue. One person had a problem in the leg. Caller doesn't think it is a characteristic of the injection. She thinks it is more the administration. She thinks she better ask her physician regarding the physiology of that. Maybe it bruised a nerve. Caller declined to do a report. Doing a report may give a false sense about the injection. If she was feeling systemically sick she would. She is leaning more towards how it was administered. Outcome of the event was unknown. No follow-up attempts are possible. Information about lot/batch number could not be requested.

Other Meds:

Current Illness:

ID: 0973498
Sex: F
Age:
State: MN

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/26/2021
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Symptoms: Fatigue; Body aches; Headache; Weakness; This is a spontaneous report from a contactable Nurse (patient). This 28-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number: Ek4176) intramuscular on 12Jan2021 11:15 at single dose on Left arm for covid-19 immunisation. The patient was not Pregnant at the time of vaccination. The patient medical history and the concomitant medications were not reported. The patient previously received first dose of BNT162B2 (lot number=Ej1685) intramuscular on 22Dec2020 at single dose on Left arm for covid-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Facility where the most recent COVID-19 vaccine was administered was Hospital. The patient experienced Fatigue, Body aches, Headache, Weakness on 13Jan2021 12:00 AM. The outcome was Recovering. No treatment received for the adverse event. All the events were assessed non-serious. Prior to vaccination, the patient was not diagnosed with COVID-19.Since the vaccination, the patient has not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 0973499
Sex: F
Age:
State:

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Onset Date:
Rec V Date: 01/26/2021
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Symptoms: arm soreness; This is a spontaneous report from a non-contactable consumer (patient). A female patient of an unspecified age received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiration date not provided), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Caller mentions that she received her second shot yesterday morning and she's got arm soreness and wanted to know if she can take Tylenol. The event was non-serious per the reporter. The outcome of the event was unknown. No follow-up attempts are possible; Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0973500
Sex: F
Age:
State: CA

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/26/2021
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Symptoms: HA; Fatigue; DOE; Chest pressure; Fever 100.2; Sudden coughing spell; This is a spontaneous report from a contactable Nurse (patient). A 62-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot number=EL3248) on 12Jan2021 18:00 at SINGLE DOSE on Left arm for covid-19 immunisation. The patient was not Pregnant at the time of vaccination. Medical history included essential hypertension (Essential HTN), cardiac output (PLR). Concomitant medication received within 2 weeks of vaccination included lisinopril. The patient previously received first dose of BNT162B2 (Lot number=EL1284) on 23Dec2020 07:00 PM at SINGLE DOSE on Left arm for covid-19 immunisation. Facility where the most recent COVID-19 vaccine was administered was Hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced Headache (HA), Fatigue, Dyspnea on effort (DOE), chest pressure, fever 100.2, sudden coughing spell that lasted hours during the night on 13Jan2021 06:30 AM. The outcome was Recovering. No treatment received for the adverse events. All the events were assessed non-serious. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds: Lisinopril

Current Illness:

ID: 0973501
Sex: F
Age:
State: MA

Vax Date: 01/01/2021
Onset Date: 01/01/2021
Rec V Date: 01/26/2021
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Symptoms: Initially a general ill feeling and then pain in the hip joint.; Initially a general ill feeling and then pain in the hip joint.; This is a spontaneous report from a contactable consumer. A 41-year-old female patient (NOT PREGNANT) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (brand: Pfizer) in Jan2021, via unknown route of administration at single dose (second dose); via unknown route of administration at single dose (first dose) in Jan2021 for unknown indication. Medical history and concomitant medications were unknown. There were unknown allergies. There was unknown if patient received other vaccine in four weeks and Other medications in two weeks. Patient experienced initially a general ill feeling and then pain in the hip joint in Jan2021. Patient did not receive any treatment. Patient did not have COVID prior vaccination and COVID tested was unknown post vaccination. The outcome of the events was recovered in Jan2021. Information on the Lot/Batch Number has been requested.

Other Meds:

Current Illness:

ID: 0973502
Sex: M
Age:
State: CA

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

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Symptoms: 2nd dose had fatigue; mild fever; body ache; tension headache; This is a spontaneous report from a contactable nurse reported for himself. A 49-year-old male patient received second dose of bnt162b2 (BNT162B2, Lot#: EJ1686), via an unspecified route of administration on 11Jan2021 on Right Arm at single dose for covid-19 immunisation. Medical history included Ulcerative Colitis. No allergies to medications, food, or other products. Concomitant medications included the patient received within 2 weeks of vaccination: Mesalamine. The patient previously took first dose of bnt162b2 (Lot#: EH9899) via Intramuscular on 21Dec2020 09:30 AM on Left arm at single dose for covid-19 immunisation. Facility where the most recent COVID-19 vaccine was administered was hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced 2nd dose had fatigue, mild fever, body ache and tension headache from 12Jan2021 06:00 AM. The outcome of the events was recovered. No treatment was received for the adverse event. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Location of injection information is available for all vaccines received on the same date.

Other Meds: Mesalamine

Current Illness:

ID: 0973503
Sex: F
Age:
State: AR

Vax Date:
Onset Date:
Rec V Date: 01/26/2021
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Symptoms: fatigue; aches; fever; This is a spontaneous report from a contactable nurse. A female patient of an unspecified age received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient received the first shot of the COVID-19 vaccine. She experienced mild symptoms-fatigue, aches, fever that subsided. This patient said that whoever administered the vaccine told her if she had this type of reaction to the first shot, that she already had antibodies and didn't need the second shot. The outcome of the events was resolving. information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973504
Sex: F
Age:
State: TX

Vax Date: 12/23/2020
Onset Date:
Rec V Date: 01/26/2021
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Symptoms: rapid test/antibody test at her work and she shows no antibodies on this test; This is a spontaneous report from a contactable nurse (patient). A 58-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 23Dec2020 as her first dose at single dose, via an unspecified route of administration on 11Jan2021 as her second dose at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took mycophenalate, hydroxychloroquin, dupixent, singulair, allegra and Pepcid, all for autoimmune disease, also took prednisone before and after her first dose of the vaccine. The patient stated that she took a rapid test/antibody test at her work and she showed no antibodies on this test. She was concerned that her use of steroids and other medications have affected her ability to produce the COVID-19 antibodies. She wanted more information on this and wanted to know if she should repeat the series. The outcome of event was unknown. Information of lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973505
Sex: F
Age:
State: NY

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 01/26/2021
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Symptoms: Pruritus; paresthesia across body, particularly extremities; This is a spontaneous report from a contactable physician. A 48-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), intramuscular on 13Jan2021 10:15 at a single dose on left arm for COVID-19 immunization. Medical history included hypertension (HTN). Concomitant medication included amlodipine besilate (NORVASC) and metoprolol tartrate (LOPRESSOR). About 8 hours after immunization, patient started to have pruritus and paresthesia across body, particularly extremities on 13Jan2021 06:00 PM. Therapeutic measures were taken as a result of the events which included Hydroxyzine Hcl (ATARAX). The outcome of the events was not recovered. The patient was not pregnant. Facility type vaccine was Nursing Home/Senior Living Facility. No other vaccine in four weeks. AE resulted in Doctor or other healthcare professional office/clinic visit. No covid prior vaccination. Not covid tested post vaccination. Information on the lot/batch number has been requested.

Other Meds: Norvasc; Lopressor

Current Illness:

ID: 0973506
Sex: F
Age:
State:

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Onset Date:
Rec V Date: 01/26/2021
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Symptoms: The injection site is red; throbbing on and off and sometimes constantly; headache; This is a spontaneous report from a contactable consumer. This consumer (patient) reported that a 33-years-old female patient received second dose of bnt162b2 (BNT162B2; PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at SINGLE DOSE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced the injection site was red, throbbing on and off and sometimes constantly, headache, all on an unspecified date with outcome of unknown. All events reported as non-serious. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0973507
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 01/26/2021
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Symptoms: mild fever; severe body aches; headache; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot no. and expiry date were not reported), via an unspecified route of administration on unspecified date at single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced the following side effects: severe body aches, headache and mild fever on unspecified date. The patient would like to know if she can take painkillers for the events. The outcome of the events was unknown. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0973508
Sex: F
Age:
State: IL

Vax Date:
Onset Date:
Rec V Date: 01/26/2021
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Symptoms: fatgiue; chills; low grade fever; pain around injection area; short time of nausea; headache; muscle pain and joint pain; muscle pain and joint pain; This is spontaneous report from a contactable consumer. This (age: 31; units: unknown) female consumer (patient) reported that she received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via unspecified route on an unknown date at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. Patient reported AE to the first dose of the covid 19 vaccine (she got the vaccine about 2 weeks ago): fatigue, chills, low grade fever, pain around injection area, short time of nausea, headache, muscle pain and joint pain. It did improve after she took paracetamol (TYLENOL) and after 24 hours, it was improved, but she was still wondering should she get 2nd dose on time or delay it. Outcome of events was recovering. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973509
Sex: F
Age:
State: MN

Vax Date: 01/13/2021
Onset Date: 01/14/2021
Rec V Date: 01/26/2021
Hospital:

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Symptoms: Heaviness in chest; Chills; Headache; Body aches; 20 Hours after vaccination; fever of 100.5; This is a spontaneous report from a contactable Nurse reported for herself. A 64-year-old female patient (not pregnant) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 13Jan2021 16:00 at single dose on left arm for COVID-19 immunisation. Medical history included Anxiety, GERD, gluten and lactose intolerant, no known allergies, no COVID prior to vaccination. There were no concomitant medications. There were no other vaccine in four weeks and no other medications in two weeks. The patient previously received the first dose of BNT162B2 in Dec2020 13:00 in Left arm for COVID-19 immunization. About 20 Hours (as reported) after vaccination, on 14Jan2021 at 11:00 AM, the patient experienced fever of 100.5, headache, body aches, heaviness in chest, chills. No treatment was received for the events. The patient had not recovered from the event. The patient didn't test COVID post vaccination. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973510
Sex: F
Age:
State: CA

Vax Date: 01/11/2021
Onset Date: 01/01/2021
Rec V Date: 01/26/2021
Hospital:

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Symptoms: runny nose; slight cough; Lethargy; very tired; no appetite; Severe body aches; chills; fever; my lymph nodes under my injection arm became swollen and sore; my lymph nodes under my injection arm became swollen and sore; This is a spontaneous report from a contactable other HCP (patient). A 62-years-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number: 0140) intramuscular in right arm on 11Jan2021 15:30 at single dose for COVID-19 immunization. She received the first dose of BNT162B2 (lot number: 0140) intramuscular in left arm on 21Dec2020 16:15 for COVID-19 immunization. Medical history included Sulfa and PCN allergy. There was no other medical history. There was no concomitant medications. There were no other medications in two weeks, no other vaccine in four weeks. The patient experienced severe body aches, chills, and fever starting approximately 8-10 hours after vaccine on 11Jan2021. These symptoms were accompanied by a runny nose and slight cough on 12Jan2021 08:00. Lethargy, very tired, no appetite also on 12Jan2021 08:00. Symptoms resolved with Tylenol, Nyquil, and one day of deep sleep. On the second day (Jan2021), her lymph nodes under her injection arm became swollen and sore. Patient is not pregnant. Events were recovered on Jan2021.

Other Meds:

Current Illness:

ID: 0973511
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 01/26/2021
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Symptoms: a painful, swollen axillary lymph node; a painful, swollen axillary lymph node; This is a spontaneous report from a contactable consumer and non-contactable consumer (patient). A patient of unspecified age and gender received the first dose of BNT162b2 (Lot/batch number and Expiration date were not provided), via an unspecified route of administration on an unspecified date at single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. A week after the first dose patient noticed a painful, swollen axillary lymph node that went away after 2-3 days. The outcome of the events was recovered on unspecified date. Information on the lot/ batch number has been requested.

Other Meds:

Current Illness:

ID: 0973512
Sex: M
Age:
State:

Vax Date: 12/30/2020
Onset Date:
Rec V Date: 01/26/2021
Hospital:

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Symptoms: This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (patient) reported that a 66-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) on 30Dec2020 at a single dose, with route of administration unspecified for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient had some neck pain. The patient had received ibuprofen (ADVIL) and paracetamol (TYLENOL) as treatment for the neck pain. The outcome of the event, neck pain, was unknown. Information about lot/batch has been requested.

Other Meds:

Current Illness:

ID: 0973513
Sex: M
Age:
State: CA

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 01/26/2021
Hospital:

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Symptoms: facial numbing; This is a spontaneous report from a contactable healthcare professional (patient). A 36-year-old male patient received his first single dose of BNT162B2 (Pfizer-BioNTech Covid-19 vaccine, lot number EJ1685) intramuscularly at 10:45 13Jan2021 at left arm for Covid-19 immunization. The patient had no known allergies and had no medical history or concomitant medications. Approximately 20 minutes after administration of the vaccine (13:15PM), the patient began to experience facial numbing, the feeling as similar to the return of sensation after having a numbing agent (at the dentist, for instance). He was more aware than usual of an effort required to move his face. It was not unpleasant, apart from being concerning- He did not know when or if this symptom might pass. Within 90 minutes of onset the sensation was 90% resolved. There was minor sensation with smiling until awakening the next day (approximately 19 hours after administration). No treatment was received for the event. The patient had no Covid-19 before vaccination and had not tested for it. The event resolved at the time of reporting (unspecified date in Jan2021).

Other Meds:

Current Illness:

ID: 0973514
Sex: F
Age:
State: TX

Vax Date:
Onset Date:
Rec V Date: 01/26/2021
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Symptoms: this was maybe an allergic reaction; itching; her face was red; her arm, it was really red; her arm, it was really puffy; This is a spontaneous report from a contactable consumer (patient). A 38-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1686), intramuscular at deltoid left on an unspecified date at single dose for COVID-19 immunization. The patient medical history was none. The patient's concomitant medication included sertraline hydrochloride (ZOLOFT), biotin and multivitamin. On an unspecified date, the patient reported that she has a lot of itching going on, people were saying her face was red, she felt itchy, it was as if she could write her name on her arm, it was really red and puffy, her left eye stated to itch, but she did not want to scratch, she thought this was maybe an allergic reaction, her pathologist gave her two ZYRTEC, she was supposed to take one, and took another one as well. Course of event was reported as follows: the patient clarified that itching started during night, her scalp started itching a little, then stomach, then she was like ok. The next, she finished working out, got a shower, she did shower and continued to itch. At work, all of a sudden, her arms started itching, then legs started, then stomach and back started itching, her coworker said it was red, face was red. It was not intolerable, but uncomfortable. The patient outcome of the events was unknown.

Other Meds: Zoloft; Biotin; Multivitamins [Vitamins Nos].

Current Illness:

ID: 0973515
Sex: F
Age:
State: RI

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

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Symptoms: Arm swelling with itchiness; Arm swelling with itchiness; warm to touch at site of injection; severe chills with shaking; severe chills with shaking; 103 fever/ approx 20hrs after injection, fever of 100 or greater for 24hrs with minimal relief with Tylenol; body aches; pains in left flank; the first dose on 20Dec2020/second dose on 12Jan2021; This is a spontaneous report from a contactable Other Healthcare Professional (patient). A 32-year-old female patient (not pregnant) received the second dose of bnt162b2 via an unspecified route of administration on 12Jan2021 10:30 AM at single dose in Left arm for COVID-19 immunisation. Medical history included cardiogenic syncope, no COVID prior vaccination. Concomitant medications included birth control drugs, no other vaccine in four weeks. The patient previously received the first dose of bnt162b2 on 20Dec2020 03:00PM on Left arm for COVID-19 immunization, topiramate (TOPAMAX) and experienced drug allergy, morphine and experienced drug allergy (hives). The patient experienced arm swelling with itchiness and warm to touch at site of injection, severe chills with shaking, 103 fever, approx. 20 hours after injection, fever of 100 or greater for 24 hours with minimal relief with Tylenol, body aches and pains in left flank. The adverse events started from 12Jan2021, 06:00 PM. Therapeutic measures taken for fever included Tylenol, no treatment was received for other events. The outcome of the events was recovering. The patient didn't test COVID post vaccination. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973516
Sex: F
Age:
State: AR

Vax Date: 12/23/2020
Onset Date: 12/24/2020
Rec V Date: 01/26/2021
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Symptoms: Fatigue; body aches; Low grade fever; This is a spontaneous report from a contactable other healthcare professional. A 27-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, solution for injection; lot/batch number and expiration date were unknown), intramuscularly on the left arm on 23Dec2020 and second dose, via an unspecified route of administration on 13Jan2021 (lot/batch number and expiration date were unknown); both at a single dose for COVID-19 immunization administered at the hospital. Relevant medical history included COVID-19 on an unknown date prior vaccination. The patient had no known allergies. There were no concomitant medications. The patient was not pregnant. The patient had no other vaccine in four weeks and had no other medications in two weeks. The patient had not tested for Covid post vaccination. On 24Dec2020, the patient experienced fatigue, body aches, and low grade fever. The patient did not receive any treatment for the events. The patient recovered from all the events on an unspecified date. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973517
Sex: F
Age:
State: IN

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

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Symptoms: Arm pain at site; Fatigue; Nausea; Body aches; This is a spontaneous report from a contactable nurse reported for herself. This 63-year-old no pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: Et1685) intramuscular on 11Jan2021 13:15 at single dose for an COVID-19 immunization. Medical history included high blood pressure. Concomitant medication included atenolol Atenolol, Losartan, Calcium, plantago ovata (METAMUCIL), bifidobacterium lactis (PROBIOTIC). Patient received the first dose of BNT162B2 intramuscular in left arm on 21Dec2020 03:30 PM. No other vaccine in four weeks. On 12Jan2021, the patient experienced Arm pain at site, Fatigue, Nausea, Body aches. No treatment received. The outcome of events was not recovered.

Other Meds: Atenolol; Losartan; Calcium; Metamucil [Plantago Ovata]; Probiotic [Bifidobacterium Lactis].

Current Illness:

ID: 0973518
Sex: F
Age:
State: NY

Vax Date: 01/10/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
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Symptoms: Tired; legs and arms felt sore; mild headache; fever 101.1; chills; This is a spontaneous report from a contactable pharmacist (patient). A 43-year-old female patient (no pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (brand=Pfizer, lot number=EK9231) on 10Jan2021 03:30 PM (vaccine location=Left arm, dose number=2) at single dose via unknown route of administration for unknown indication. Medical history was not reported. Concomitant medications included ibuprofen (MOTRIN); vitamins NOS (MVI); calcium carbonate, colecalciferol (OSCAL D); vitamin c. Historical vaccine included patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (brand=Pfizer, lot number=Ek5730), on 19Dec2020 03:15 PM, (vaccine location=Left arm, dose number=1) via unknown route of administration at single dose for unknown indication. There were unknown allergies. Patient did not receive other vaccine in four weeks. Patient did not have covid prior vaccination and did not have covid tested post vaccination. Patient experienced Tired, legs and arms felt sore, mild headache, fever 101.1, chills on 11Jan2021 01:30 PM. Patient did not receive any treatment. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: Motrin [Ibuprofen]; mvi [Vitamins Nos]; Oscal D [Calcium Carbonate; Colecalciferol]; Vitamin C [Ascorbic Acid].

Current Illness:

ID: 0973519
Sex: M
Age:
State: OH

Vax Date: 01/06/2021
Onset Date: 01/07/2021
Rec V Date: 01/26/2021
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Symptoms: body aches; a fever of 101; This is a spontaneous report from a contactable nurse (patient). A 48-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number not provided), intramuscularly on 06Jan2021 10:00 at single dose for covid-19 immunization. Vaccine location was left arm and it was the second dose. Patient received the first dose in Dec2020 10:00 intramuscular at left arm for covid-19 immunization. The facility type vaccine was hospital. The patient medical history was not reported. Concomitant medication included bupropion hydrochloride (WELLBUTRIN), emtricitabine, tenofovir disoproxil fumarate (TRUVADA). Patient was not diagnosed with COVID-19 prior to vaccination nor tested for COVID-19 since the vaccination. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced body aches and a fever of 101 on 07Jan2021 14:00. He fully expected this immune response from his body and it only lasted 12-24 hours. Patient didn't receive treatment for the adverse events. The outcome of events was recovered in 08Jan2021. The events were reported as non-serious. Information about Batch/Lot number has been requested.

Other Meds: WELLBUTRIN; TRUVADA

Current Illness:

ID: 0973520
Sex: F
Age:
State:

Vax Date: 01/09/2021
Onset Date: 01/10/2021
Rec V Date: 01/26/2021
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Symptoms: chills; muscle ache; low grade fever up to 100.3; a red flushed rash on neck and chest; This is a spontaneous report from a contactable nurse (patient). A 39-year-old non-pregnant female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231), via an unspecified route of administration on 09Jan2021 12:00 at single dose in left arm for covid-19 immunization. The patient had no other medical history and no known allergies. Concomitant medication included vitamin D3 and daily multivitamin. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL0140), on 20Dec2020 07:30 in left arm for covid-19 immunization. The patient had no covid prior vaccination and no covid tested post vaccination. The patient reported that on 10Jan2021 02:00 about 14 hours after 2nd vaccine she had chills, muscle aches, and low grade fever up to 100.3 for the next 12 hours. Then she experienced a red flushed rash on neck and chest for about 12 hours after the previous symptoms. All symptoms gone after about 24 hours. The patient did not receive any treatments for events. The outcome of the events was recovered on 11Jan2021.

Other Meds: VITAMIN D3

Current Illness:

ID: 0973521
Sex: F
Age:
State: AK

Vax Date: 12/18/2020
Onset Date: 12/19/2020
Rec V Date: 01/26/2021
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Symptoms: could not get up from the bed; she did not feel well; This is a spontaneous report from a contactable consumer (patient). A 41-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via unspecified route in left arm single dose for prevent COVID on 18Dec2020 at 07:00am, at 41-year-old. Medical history included: seizures from 2014. Concomitant medication included: ongoing topiramate oral 50mg one tablet in the morning and two tablets in the evening for seizures; levetiracetam (KEPPRA). No additional vaccines administered on same date of BNT162B2. She was okay on 19Dec2020. After mid-day around noon (19Dec2020) she did not feel well, and it was hard for her to work on the 19th. She missed two days of work. On 20Dec2020 she could not get up from the bed. Emergency Room or Physician Office not visited. No relevant tests done. Action taken for BNT162B2 was not applicable. Outcome of the event was unknown. Information about lot/batch number has been requested.

Other Meds: Topiramate; Keppra

Current Illness:

ID: 0973522
Sex: M
Age:
State: OH

Vax Date: 01/08/2021
Onset Date: 01/01/2021
Rec V Date: 01/26/2021
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Symptoms: he wasn't attracted to food for a day; arm began hurting at the right top of his arm and right shoulder area; planned in 2 weeks, will be his second COVID-19 Vaccine shot; This is a spontaneous report from a contactable Consumer(patient). The 94-year-old male patient received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration at right arm on 08Jan2021 at single dose for COVID-19 immunization in a nursing home. Medical history included he was hospitalized with the COVID-19 Virus and pneumonia in Apr2020. He was in the hospital for 2 weeks, the hospital treated him one COVID-19 Vaccine (he doesn't know what they did in the hospital when he had the COVID-19 Virus in Apr2020), then he went to rehab for 6 weeks, he was gone from his residence for a total of 8 weeks, he also had throat problem, and a swallowing issue for a long time before he received the COVID-19 Vaccine, he had a constant clearing of his throat. He had tiny bits of bacon that may cling on to the edge of his throat, and block his swallowing temporarily. Once he cleared his throat, he went back to swallowing. When he cleared his throat, it took care of his swallowing problem, but not permanently. The patient's concomitant medications were not reported. The patient experienced His arm began hurting at the right top of his arm and right shoulder area after receiving the COVID-19 Vaccine (where he received the COVID-19 Vaccine) on 08Jan2021. He said everything was OK, he was feeling some pain, but the pain was nothing to even keep him awake. The next day after receiving the vaccine(09Jan2021), he had no desire for any food, and didn't eat anything, he didn't want anything to eat/ he wasn't attracted to food for a day. He was having a recap of the effect of getting the Vaccine shot. He said the COVID-19 Vaccine shot affected his stomach's desires and so forth. He had been eating now for the past 2 days. There was no treatment received. He also clarified under the COVID-19 Vaccine program with Pfizer, the COVID-19 Vaccine shot planned in 2 weeks, will be his second COVID-19 Vaccine shot. He said the COVID-19 Vaccine is so new, and people are on a tight schedule to get the COVID-19 Vaccine shot. Outcome of arm began hurting and Appetite lost was recovered in Jan2021. Information on the lot/batch number has been requested.

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Current Illness:

ID: 0973523
Sex: M
Age:
State: LA

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
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Symptoms: Weak; Chills and completely ice cold; Chills and completely ice cold; Really sore in injection arm; Joints hurt; This is a spontaneous report from a contactable consumer (patient). This 76-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 11Jan2021 12:00 on arm Left at single dose for covid-19 immunisation. Lot number is EL3, then a number he cannot read, followed by 46. Medical history included type 2 diabetic. No concomitant medications. His joints hurt on 11Jan2021 in later afternoon. It is not worse, but not better. On 12Jan2021, chills and Woke up during night completely ice cold. Had to get a blanket and finally went back to sleep. Feels weak. Doesn't know what happened. Still feels chill. After midnight on the 12Jan2021. Is a little bit better. He was really sore in injection arm on 11Jan2021. Outcome of the event Joints hurt was not recovered. Outcome of the events Chills and completely ice cold was recovering. Outcome of the event Really sore in injection arm was not recovered. Outcome of the event Weak was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973524
Sex: F
Age:
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Rec V Date: 01/26/2021
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Symptoms: Mild fever; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number and Expiration Date were not reported), via an unspecified route of administration, on an unspecified date, at a single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient got the first shot of the COVID-19 vaccine and is experiencing a mild fever. The event was considered non-serious. The outcome of the event was unknown. Information about lot number and expiration date for the suspect product will be requested in follow-up attempts.

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Current Illness:

ID: 0973525
Sex: F
Age:
State: WI

Vax Date: 01/07/2021
Onset Date: 01/07/2021
Rec V Date: 01/26/2021
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Symptoms: Tender; Swollen glands, neck, face, and ear on left side/ glands on left side of neck were swollen; Swollen glands, neck, face, and ear on left side; Swollen glands, neck, face, and ear on left side; Swollen glands, neck, face, and ear on left side; Cold, chills, and felt like freezing to death; Cold, chills, and felt like freezing to death; Felt like drunk driving; Cold, chills, and felt like freezing to death; Severe headache; Dizziness; This is a spontaneous report from a contactable consumer (patient). A 55-year-old female patient received bnt162b2 (PFIZER- BIONTECH COVID-19 VACCINE) at left arm, via an unspecified route of administration on 07Jan2021 11:45 at single dose for covid-19 immunisation. Medical history included rheumatoid arthritis (RA). The patient's concomitant medications were not reported. The patient experienced cold, chills, and felt like freezing to death, felt like drunk driving, severe headache and dizziness on 07Jan2021; swollen glands, neck, face, and ear on left side on 12Jan2021; tender on an unspecified date. The patient received COVID-19 Vaccine on 07Jan2021 at approximately 11:45. She felt like drunk driving: She waited the 15 minutes and was fine. Afterwards, she got into her truck and was literally weaving. Had to really concentrate to keep the truck in a straight line. She had severe headache: Did not go into work on Friday because headache was so bad. It was almost a migraine. She could still feel it, but it was not as severe. Patient known it's five days out, but yesterday (12Jan2021) she got up and glands on left side of neck were swollen. That side of her face and ear was swollen. It was very pronounced. She still swollen today (13Jan2021). Patient stated she worked with dementia and didn't know if she should go into work when she was still swollen and tender. The patient took Benadryl (Lot: P119936, Exp: Apr2023) as Equate Allergy Relief at 25mg, two capsules at night for the reaction. The patient had been taking it every night since she received the COVID-19 Vaccine. Headache was still there. This morning woke up with swollen glands, neck, ear, and face on the left side. The outcome of events "cold, chills, and felt like freezing to death" and dizziness was recovered on 10Jan2021; of event "Felt like drunk driving" was recovered on an unspecified date; of event severe headache was recovering; of event "Swollen glands, neck, face, and ear on left side" was not recovered; of event Tender was unknown. Information on Lot/Batch number has been requested.

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Current Illness:

ID: 0973526
Sex: M
Age:
State: MA

Vax Date: 12/28/2020
Onset Date: 12/30/2020
Rec V Date: 01/26/2021
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Symptoms: Sore arm at injection site; cold sore; Sore throat; This is a spontaneous report from a non-contactable Pharmacist(patient). The 26-year-old male patient received first dose BNT162B2(Covid 19, lot EK5730), via an unspecified route of administration at left arm on 28Dec2020 17:15 at single dose for COVID-19 immunization in hospital. Medical history included last cold sore was over 2 years ago. There was no other vaccine in four weeks. There was no known allergies, no other medical history. There were no concomitant medications. The patient experienced sore throat occurred 2 days after vaccination(30Dec2020), sore arm at injection site, cold sore appearance 8 days after vaccination, both on 05Jan2021. There was no treatment. There was no covid prior vaccination, covid tested post vaccination was Nasal Swab with PCR on 08Jan2021 with negative result. Outcome of events was recovered in Jan2021 . No follow-up attempts are possible. No further information is expected.

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Current Illness:

ID: 0973527
Sex: F
Age:
State: NC

Vax Date: 01/07/2021
Onset Date: 01/08/2021
Rec V Date: 01/26/2021
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Symptoms: Fever; Headache; Chills; This a spontaneous report from a Pfizer-sponsored program by a contactable consumer (patient). A 77-years-old female patient received first dose of bnt162b2 (Covid-19 vaccine, Batch/lot number: EL3246), via an unspecified route of administration on 07Jan2021 at SINGLE DOSE on left arm for covid-19 immunisation. Medical history included ongoing blood pressure. Concomitant medication included amlodipine (AMLODIPINE), bisoprolol fumarate/hydrochlorothiazide (BISOPROLOL/HYDROCHLOROTHIAZID), both since 2015 and ongoing for blood pressure. The patient experienced fever, headache, chills on 08Jan2021. Everything happened at night time. Her temperatures have been 100.4 and 100.5 degrees. The headache only lasted for a couple of days. It was also only at night. The patient underwent lab tests and procedures which included blood pressure measurement: fine on 12Jan2021, body temperature: 100.4 and 100.5 degrees on an unknown date. The event outcome of fever, headache was not recovered; outcome of chills was recovering.

Other Meds: Amlodipine; Bisoprolol/Hydrochlorothiazide

Current Illness: Blood pressure abnormal

ID: 0973528
Sex: F
Age:
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Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 01/26/2021
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Symptoms: fever 102.7; muscle pain; generalized fatigue; This is a spontaneous report from a non-contactable nurse (patient). An adult female patient received COVID-19 vaccine (UNSPECIFIED TRADE NAME, lot# EK9231), via an unspecified route of administration on 08Jan2021 07:45 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient was not pregnant. If other vaccine in four weeks: No. Twelve hours after the patient received vaccine on 08Jan2021 20:00, the patient developed fever 102.7, muscle pain and generalized fatigue. All symptoms lasted about 24 hours. The patient underwent lab tests and procedures which included body temperature: 102.7 on 08Jan2021. The patient received treatment ibuprofen (MOTRIN) for all the events. If-covid-prior-vaccination: No. If covid tested post vaccination: No. The outcome of all the events was recovered on 09Jan2021. AE was not resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0973529
Sex: F
Age:
State: IL

Vax Date: 01/10/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
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Symptoms: Left arm pain in armpit; swollen lymph nodes; led to whole left arm pain; This is spontaneous report from a contactable nurse (patient). A 48-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) intramuscular on left arm single dose for COVID-19 immunization on 10Jan2021, 09:30 AM, at 48-year-old. Medical history and concomitant medication were not reported. No known allergies. The patient did not have COVID prior vaccination. The patient did not have other vaccine in four weeks. The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) intramuscular on left arm for COVID-19 immunization on 20Dec2020, 05:30 PM, at 48-year-old. On 11Jan2021, 05:00 PM, the patient had left arm pain in armpit with swollen lymph nodes, led to whole left arm pain. No treatment received. The patient was not tested for COVID post vaccination. Action taken for BNT162B2 was not applicable. Outcome of the events was not resolved. Information on the lot/batch number has been requested.

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Current Illness:

ID: 0973530
Sex: F
Age:
State: CA

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
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Symptoms: Extreme body achees; Severe headache; lymphadenopathy in the armpit.; This is a spontaneous report from a contactable nurse (patient). A 46-year-old female patient (no pregnancy) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscularly at site of left arm at 10:30 on 11Jan2021 at single dose for COVID-19 immunization. The patient's medical history was not reported. There were no concomitant medications. The patient previously took first dose of BNT162B2 on an unspecified date. The patient experienced extreme body achees, severe headache, lymphadenopathy in the armpit, all at 21:30 on 11Jan2021. Adverse reactions did not result any serious consequences. Facility type vaccine was hospital. No need treatment for adverse event. No covid prior vaccination. No covid tested post vaccination. No known allergies. Other medical history was none. The outcome of events was recovering. Information on the lot/batch number has been requested.

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Total 2021 VAERS Injuries: 599,999

Page last modified: 03 October 2021 5:28pm