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
46,870MODERNA
532GLAXOSMITHKLINE BIOLOGICALS
353PFIZER\BIONTECH
231MERCK & CO. INC.
221UNKNOWN MANUFACTURER
62SEQIRUS, INC.
25DYNAVAX TECHNOLOGIES CORPORATION
13EMERGENT BIOSOLUTIONS
12SANOFI PASTEUR
9NOVARTIS VACCINES AND DIAGNOSTICS
5PFIZER\WYETH
5PAXVAX
2TEVA PHARMACEUTICALS
2PROTEIN SCIENCES CORPORATION
1BERNA BIOTECH, LTD.
1INTERCELL AG
1CSL LIMITED

COVID19 Lot Number

VAX LOT Total
2S9CL1,906
1,575
289
IMM209286
252
236
229
s029456178
171
UT7065MA166
155
149
145
S034636133
107
U62828AA103
100
98
P10025327596
U6737AA85
UJ446AA79
78
78
59
57
4BH3254
4F47253
52
27656352
50
PP9L548
49TM346
42
40
38
MENVEO38
4F47237
R1B252M36
34
C5763AA30
93362229
25
300057A24
UNK24
22
CW311621
18
17
15
UH894AB15
3Y7NL12
R1B743M12
EJ168611
el128410
10
10
10
9
ARBA141A9
UNK9
8
UNK8
8
1F4EB8
Unknown7
7
No batch number6
5
5
UJ090AA5
5
5
4
4
4
UNK4
JEV18K95E4
UNK3
A115A3
Z127A3
3
3333324181073
2
2
2
TAR352
1
1
1
1
1
A739081
1
1
1
1
1
037K20A68,542
EL128447,700
133

Incidents per State

State Total
15,185
CA14,096
NY7,507
TX7,196
FL6,939
IN5,527
PA4,560
IL4,179
OH4,054
AZ3,856
MI3,771
NJ3,411
MA3,278
VA3,208
NC3,114
WA3,034
GA2,864
MD2,652
MN2,534
CO2,532
WI2,457
MO2,029
OR1,943
TN1,715
CT1,693
KY1,603
OK1,226
AL1,201
KS1,162
IA1,157
SC1,106
NM1,065
UT973
AR951
LA945
NE829
NV797
ME795
MT789
NH756
ID674
AK661
WV661
PR650
MS585
HI536
RI510
VT441
SD361
ND356
DE350
DC239
WY209
GU32
AS16
VI13
MP9
MH3
FM2
QM1
XB1

ID: 0993821
Sex: M
Age:
State: NC

Vax Date:
Onset Date: 01/18/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: nauseated; vomited; This is a spontaneous report from a contactable nurse. A 78-year-old male patient (reporter's husband) received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247), via an unspecified route of administration in the right arm on an unspecified date at a single dose for COVID-19 immunization. Medical history included dialysis from an unknown date (also reported as started about two years ago). There were no concomitant medications. The patient got real nauseated and vomited, states he got sick last night on 18Jan2021 and today it was much improved. Outcome of the events was recovering.

Other Meds:

Current Illness:

Date Died:

ID: 0993822
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: he got both doses then a few days later he died; This is a spontaneous report from a contactable consumer reporting for a friend's father. A male patient of an unspecified age received the second dose of bnt162b2 (BNT162B2) vaccine , via an unspecified route of administration on an unspecified date at single dose for Covid-19 immunisation . The patient medical history and concomitant medications were not reported. The patient received the first dose on an unknown date. The patient died few days after receiving the second dose of the vaccine on an unspecified date. It was not reported if an autopsy was performed. Information about lot/batch number has been requested.; Reported Cause(s) of Death: he got both doses then a few days later he died

Other Meds:

Current Illness:

Date Died:

ID: 0993823
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: died due to heart attack; This is a spontaneous report from a contactable consumer (reporting for her son-in-law) from the Pfizer-sponsored program Pfizer First Connect. A male patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patients medical history and concomitant medications were not reported. The patient died due to heart attack on an unspecified date. The patient died on an unspecified date. It was unknown if an autopsy was performed. Follow-up (28Jan2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts completed. No further information is expected.; Reported Cause(s) of Death: died due to heart attack

Other Meds:

Current Illness:

ID: 0993824
Sex: M
Age:
State: NJ

Vax Date: 01/18/2021
Onset Date: 01/19/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: loss of hearing; This is a spontaneous report from a contactable consumer. An 80-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 18Jan2021 12:00 PM at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. It was unknown if patient had COVID prior vaccination. The patient experienced loss of hearing the day after vaccination administered on 19Jan2021. It was unknown if treatment was received and unknown if patient had tested COVID post vaccination. The outcome of event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0993825
Sex: F
Age:
State: PA

Vax Date: 01/18/2021
Onset Date: 01/19/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data: Test Date: 20210119; Test Name: Nasal Swab; Result Unstructured Data: Test Result:Unknown

Allergies:

Symptoms: Day after receiving 2nd dose, patient developed facial congestion, burning eyes, scratchy throat.; Day after receiving 2nd dose, patient developed facial congestion, burning eyes, scratchy throat.; Day after receiving 2nd dose, patient developed facial congestion, burning eyes, scratchy throat.; This is a spontaneous report from a contactable pharmacist reported a female patient. A 51-year-old female patient receive the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number /expiration date: unknown), via Intramuscular route of administration, on 18Jan2021 03:15 PM (at the age of 51 years old) as a single dose on left arm for COVID-19 immunisation at a workplace clinic. Relevant medical history included thyroid removed 30+ years (onset date unknown). Historical vaccine included fist dose of BNT162B2 (Pfizer Covid-19 vaccine, lot#/exp. date unknown) via Intramuscular route of administration on left arm. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient was not pregnant at time of vaccination. Concomitant medications included levothyroxine sodium (SYNTHROID). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 19Jan2021, the patient stated that day after receiving 2nd dose, she developed facial congestion, burning eyes, scratchy throat. She proceeded to get COVID Nasal Swab test on 19Jan2021 with unknown result at time of report. Patient stated workplace did not believe they were adverse reaction to vaccine. The patient received treatment no treatment. The outcome of the events facial congestion, burning eyes, scratchy throat was recovering. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds: SYNTHROID

Current Illness:

ID: 0993826
Sex: F
Age:
State: FL

Vax Date: 12/28/2020
Onset Date: 12/28/2020
Rec V Date: 02/02/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: coronavirus; Test Result: Negative

Allergies:

Symptoms: She is being told that one of the nurses at the outpatient clinic where she works was positive for COVID.; right arm soreness at the injection site with the first dose; This is a spontaneous report from a contactable nurse (patient). A 67-year-old female nurse received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EK9231) via intramuscular in right arm on 28Dec2020 09:52 at single dose for COVID -19 immunisation. Medical history and concomitant medications were not reported. She does not have any health issues or chronic health conditions. Patient was calling about the COVID-19 vaccine. She is a Registered Nurse. She reported right arm soreness at the injection site with the first dose at the first day (28Dec2020). Nurse declined any treatment. Nurse provided seriousness assessment for right arm soreness at the injection site with the first dose: Not serious. She tested negative for coronavirus that Monday prior to the surgery (11Jan2021). She is being told that one of the nurses at the outpatient clinic where she works was positive for COVID. Patient just had rotator cuff repair surgery last Thursday (14Jan2021). She is on pain medicine from her surgery. She is taking hydrocodone acetaminophen 10/325mg and a muscle relaxer called methocarbamol but she does know the dose. She is not having pain at her site of her surgery. She had the second dose on 19Jan2021 11:03. Patient did not have additional vaccines administered on same date of the Pfizer vaccine. Patient did not visit emergency room nor physician office. No prior vaccinations within 4 weeks. Outcome of the events was unknown.

Other Meds:

Current Illness:

Date Died: 01/24/2021

ID: 0993828
Sex: M
Age:
State: FL

Vax Date: 01/21/2021
Onset Date: 01/24/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data: Test Date: 20210124; Test Name: blood sugar; Result Unstructured Data: Test Result:91; Test Name: blood pressure; Result Unstructured Data: Test Result:fine; Test Name: heart test; Result Unstructured Data: Test Result:perfect; Test Name: A1C; Result Unstructured Data: Test Result:was always high

Allergies:

Symptoms: Heart stopped; Could not swallow; This is a spontaneous report from a contactable nurse (patient's wife). An 85-year-old male patient received the first dose of the bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on 21Jan2021 at a single dose for COVID-19 immunization. Medical history included blood pressure abnormal (verbatim: blood pressure) from an unknown date and unknown if ongoing, neuropathy from an unknown date and unknown if ongoing, weight issue from an unknown date and unknown if ongoing, diabetes from an unknown date and unknown if ongoing, walker user from an unknown date and unknown if ongoing. Concomitant medications included insulin aspart (NOVOLOG) taken for diabetes from an unspecified date to an unspecified date; and he was taking a long acting one as well. The patient previously received the influenza vaccine (MANUFACTURER UNKNOWN) for immunization on unknown dates ("had flu shots before with no reactions and everything, nothing before"). On 24Jan2021, the patient's heart stopped (death, medically significant), and could not swallow (medically significant). The clinical course was reported as follows: The patient's wife stated the patient was taking insulin aspart (NOVOLOG) and he was taking a long acting one as well. The reporter, the patient's wife and a retired registered nurse (RN) stated, her husband (patient) just died and she thought he died from the COVID vaccine (later clarified the reason of death was-heart stopped). The patient had the vaccine on 21Jan2021, which was on a Thursday, and he was fine. On the following Sunday around 1:30 (on 24Jan2021), the patient was feeling a little weak, however, the patient's wife thought maybe his blood sugar was low. The patient's wife checked, and the patient's blood sugar was 91. The patient's wife went to get some yogurt to feed him in order to get his blood sugar up a little; "which was a normal thing for him, it was not that low for him." Then, suddenly, the patient fell, and the patient's wife could not get a pulse or anything. The patient's wife called an unspecified number and she started compressions; however, he was dead. The patient's wife stated the patient just had his heart test, a three hour long one, and it was "perfect three weeks ago." The patient had just gone to the doctor the other day and his blood pressure was "fine and everything." The patient's wife stated that other than his diabetes, "which he had for (sentence incomplete)." Regarding lab tests, the patient's wife stated, "No, he had it before but not in the last two weeks. He was going for one because we just went to the doctor last week and he was going to call yesterday to make the appointment request to get his blood work done. Blood work has been good except his A1C was always high, but other than that everything was good" (as reported). Regarding causality, the patient's wife stated, "I do, because he was fine until about half an hour before he died. He said to me, I feel a little weak today and then I was talking to him that your upper body strength is really good and then I said, we just have to work on your weight a little more because he did have neuropathy. And then, I went out of the room and all of a sudden I just heard him fall and that is when I just went in to check his blood sugar and it was 91 and I got him yogurt and he started eating that and then that was it, he started spitting it out and he said, I could not swallow and that was it, he just died." The patient's wife further added, "I just wanted other people to know that things like this happen and I am sure it was from that because he was healthy as could be. He was walking with his walker, the day before outside and he felt fine." The clinical outcome of the event, heart stopped, was fatal. The clinical outcome of the event, could not swallow, was unknown. The patient died on 24Jan2021 due to "heart stopped." An autopsy was not performed. The batch/lot numbers for the vaccine, PFIZER-BIONTECH COVID-19 MRNA VACCINE, were not provided and will be requested during follow up.; Reported Cause(s) of Death: Heart stopped

Other Meds: NOVOLOG

Current Illness:

ID: 0993829
Sex: F
Age:
State: FL

Vax Date: 01/14/2021
Onset Date: 01/16/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Itchy hives; This is a spontaneous report from a contactable other health professional (Child life specialist) reporting for herself. A 32-year-old female patient received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231), via an unspecified route of administration on 14Jan2021 at single dose for COVID-19 immunization. Medical history included depression. Concomitant medication included fluoxetine for anti depressant. Patient stated, "I am here to report side effect with the vaccine (Later clarified as Covid Vaccine Pfizer). 48 hours after getting the vaccine, itchy hives (on 16Jan2021)." Treatment received for the event included Cortisone and Benadryl. The outcome of the event was unknown. Causality reporter stated, "Yes."

Other Meds: FLUOXETINE

Current Illness:

ID: 0993830
Sex: F
Age:
State: PA

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data: Test Name: blood work; Result Unstructured Data: Test Result:Unknown Results; Comments: I don't know, I guess I just look into, I need more time to gather that information, I don't have it; Test Name: lab work; Result Unstructured Data: Test Result:Unknown Results; Comments: be not sure 2 to 3 weeks, I have been feeling lot of fatigue

Allergies:

Symptoms: Loss of taste; Tightening in the jaw; Tightening is on the side where the forehead is and the front like on the two sides is the pressure on the side of the head; just thinking of a headache; I have been feeling lot of fatigue; crying; This is a spontaneous report from a contactable consumer. This consumer reported for herself that the 63-year-old female patient received first dose of bnt162b2 (Unspecified Shot), via unknown route of administration on 15Jan2021 at single dose for covid-19 immunisation (to make sure because I am a caregiver). Medical history included Sjoegren's syndrome and had like chronic fatigue but "that is not a real thing". Concomitant medications included buspirone hydrochloride (BUSPAR) and other medications that she just take a half every other day, it is a small amount. She take 5 mg every other day. She was really taking much. The consumer had lab work, may be not sure 2 to 3 weeks, she has been feeling lot of fatigue. Actually, she did do lab work, it was just like lot of blood work. The consumer stated, "I am having some loss of taste and tightening in the jaw and that was immediately. Tightening is still there and the taste loss seems to happen like a day later. Tightening is on the side where the forehead is and the front like on the two sides is the pressure on the side of the head. I guess, just thinking of a headache. I guess, I had headache and crying, it is just nerve-racking." The events started from 15Jan2021 with outcome of not recovered. Treatment received included Advil. Information on the batch number/lot number has been requested.

Other Meds: BUSPAR

Current Illness:

ID: 0993831
Sex: F
Age:
State: MA

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data: Test Date: 20210125; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: After I have the Pfizer vaccine, with 15 minutes I started having a small cough. The cough increased; my throat swollen; hard to breath; This is a spontaneous report from a contactable other hcp (patient). A 36-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number: El9261) at left arm via an unspecified route of administration on 22Jan2021 15:00 at single dose for COVID-19 immunization. Medical history included known allergies: Apple, pear, peach, pineapple, mango, avocado and almonds. Concomitant medications included unspecified multivitamins. No other vaccine in four weeks. After patient had the bnt162b2, with 15 minutes she started having a small cough on 22Jan2021 15:15. The cough increased, her throat swollen and hard to breath on 22Jan2021 15:15. The nurse immediately gave her the epi pen and Benadryl. She had to rush to the ER. When she got there, she needed to have the second round of epi pen and more Benadryl. Events resulted in life threatening illness (immediate risk of death from the event). No covid prior vaccination. The patient was not pregnant at time of vaccination. The patient underwent lab tests and procedures, which included Nasal Swab on 25Jan2021 with result of negative. The outcome of the events was recovering.; Sender's Comments: Based on temporal association, a possible contributory role of BNT162B2 cannot be excluded for reported events cough, throat swelling and difficulty breathing. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds:

Current Illness:

Date Died:

ID: 0993832
Sex: U
Age:
State: ME

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

Lab Data:

Allergies:

Symptoms: At the end of the conversation, caller stated that recently saw in (place name) that someone passed away 3 hours after receiving the injection.; This is a spontaneous report from a contactable nurse. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on unspecified date at single dose for COVID-19 immunization. Medical history and concomitant medication were not reported. Caller, calling on behalf of her sister who has pseudocholinesterase imbalance, would like to know if the Covid vaccine has any contraindication or interaction with succinylcholine. Caller stated that her and her sister are scheduled to receive the first dose of the vaccine this weekend. Caller stated that her sister had a severe reaction to succinylcholine and did not wake up for four days. Caller stated that her sister has to wear a medical bracelet because of this condition. Caller reported that her sister's son has the same severe reaction to succinylcholine. Caller also stated that when she was a director in the lab, she heard of a person passing away in the OR due to the same reaction with succinylcholine. At the end of the conversation, caller stated that recently saw in (state name) that someone passed away 3 hours after receiving the injection. It was unknow if autopsy was done. Information on the lot/Batch number has been requested.; Sender's Comments: The information currently available does not allow a medically meaningful assessment for the event "passed away" with unknown cause of death. The case will be reassessed should additional information become available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics committees and Investigators, as appropriate.; Reported Cause(s) of Death: At the end of the conversation, caller stated that recently saw in (place name) that someone passed away 3 hours after receiving the injection.

Other Meds:

Current Illness:

ID: 0993833
Sex: F
Age:
State: FL

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

Lab Data: Test Date: 202101; Test Name: Covid-19; Test Result: Positive ; Comments: She received her first dose of the Covid vaccine and then tested positive for Covid

Allergies:

Symptoms: She received her first dose of the Covid vaccine and then tested positive for Covid; She received her first dose of the Covid vaccine and then tested positive for Covid; This is a spontaneous report from a Pfizer sponsored program. A contactable 27-year-old female other HCP (medical assistant, patient) received 1st of BNT162B2 (Batch/lot number: EK5730) Intramuscular on 04Jan2021 at single dose (0.3 ml) for covid-19 immunization. Medical history and concomitant drug were not reported. She received her first dose of the Covid vaccine and then tested positive for Covid. She was calling to see what she should do about the second dose. Outcome of the event was unknown. No follow-up attempts possible. No further information expected.; Sender's Comments: Based on available information, a possible contributory role of BNT162B2 cannot be completely excluded for reported "tested positive for Covid".

Other Meds:

Current Illness:

ID: 0993834
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Contacted Covid after their first vaccine; Contacted Covid after their first vaccine; This is a spontaneous report from a Pfizer sponsored program from a contactable consumer. The consumer reported similar events for two patients. This is the first of two reports. A patient of unspecified age and gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose on an unspecified date for COVID-19 immunisation. Medical history and concomitant medication were not reported. Patient contacted COVID after their first vaccine. The outcome of events was unknown. Information on lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021086942 the same reporter, product and similar adverse events in different patients

Other Meds:

Current Illness:

ID: 0993835
Sex: F
Age:
State: CO

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

Lab Data:

Allergies:

Symptoms: moderate L arm pain; intermittent mild moderate retro orbital and tension headache; intermittent mild moderate retro orbital and tension headache; Difficulty sleeping with multiple awaking; Difficulty sleeping with multiple awaking; This is a spontaneous report from a contactable Physician (patient). A 29-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL1284 and expiration date: 30Apr2021), intramuscular in left deltoid on 08Jan2021 09:00 at a single dose for COVID-19 immunization. Medical history included Menorrhagia. Concomitant medication included ongoing Mirena IUD from 04Jun2020 ('Once placed last 5 yr') for pregnancy prevention and menorrhagia. On 08Jan2021 (at PM), the patient developed moderate left (L) arm pain which improved gradually and resolved 10Jan2021 (at AM), significantly less severe than prior. Patient had intermittent mild moderate retro orbital and tension headache occurred 08Jan2021 (at PM) thru 10Jan2021 (at AM). Patient had difficulty sleeping with multiple awaking on 08Jan2021 to 09Jan2021 overnight. The patient was not admitted to the hospital. The reporter reported a reasonable possibility that the events were related to suspect product. No treatment was required. The outcome of the events moderate left (L) arm pain and retro orbital and tension headache was recovered on 10Jan2021; event difficulty sleeping with multiple awaking was recovered on 09Jan2021.

Other Meds: MIRENA

Current Illness:

ID: 0993836
Sex: F
Age:
State: MI

Vax Date: 12/29/2020
Onset Date:
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Right sided supraclavicular lymph node enlargement and pain; Right sided supraclavicular lymph node enlargement and pain; This is a spontaneous report from a contactable nurse reporting for herself. A 40-year-old female patient received the 1st dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech) (lot# EJI1686), intramuscular in right arm, on 29Dec2020, at single dose, for COVID-19 immunisation. The patient's medical history was not reported. The patient was not diagnosed with COVID-19 prior to vaccination. Concomitant medications included celecoxib (CELEXA), vitamin d [vitamin d nos] (unknown manufacturer), post natal vitamin. No any other vaccine within 4 weeks prior to the COVID vaccine was administered. The patient previously took butorphanol tartrate (STADOL) and experienced drug hypersensitivity. The patient experienced right sided supraclavicular lymph node enlargement and pain on an unspecified date with outcome of recovering. No treatment was given. The patient has not been tested for COVID-19 since the vaccination.

Other Meds: CELEXA [CELECOXIB]; VITAMIN D [VITAMIN D NOS]

Current Illness:

ID: 0993837
Sex: M
Age:
State: AZ

Vax Date: 01/18/2021
Onset Date:
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: having really severe pain in his armpit as well as his spleen; having really severe pain in his armpit as well as his spleen; Fever; This is a spontaneous report from a contactable consumer (patient). A 36-years-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number: EL1283), on 18Jan2021 10:10 at single dose for COVID Prophylaxis. Medical history included Hyperlipidemia, Attention deficit disorder. Concomitant medication included atorvastatin at 20 mg for Hyperlipidemia, amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL) Extended release at 10 m for Attention deficit disorder. The patient previously received first dose of BNT162B2 on unknown date at single dose for Covid prophylaxis. The patient received his second dose at 10:10 am on 18Jan2021. The patient has had some of the symptoms as the first vaccine. But just now he was having really severe pain in his armpit as well as his spleen. He also had a low grade fever at this time around. He took 650 mg Tylenol, Twice a day as treatment. The outcome of fever was unknown, of other events were not recovered.

Other Meds: ATORVASTATIN; ADDERALL

Current Illness:

ID: 0993838
Sex: F
Age:
State: CA

Vax Date: 01/16/2021
Onset Date: 01/16/2021
Rec V Date: 02/02/2021
Hospital: Y

Lab Data:

Allergies:

Symptoms: severe itching; had some different allergies; This is a spontaneous report from a contactable nurse (patient). A 56-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 16Jan2021 at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient got the first dose of BNT162B2 for COVID-19 immunisation on 28Dec2020, and the patient had no side effects. The patient got the second COVID shot (vaccine) and she had a reaction to it, she had some different allergies and she got severe itching on 16Jan2021, admitted into emergency room from 16Jan2021 to 16Jan2021. Seriousness of the events was hospitalization. The patient stayed at the site for a while because the itching didn't end they wanted the patient to go into an Emergency Room (ER) but they were able to get it under control and the patient was fine today. The patient received diphenhydramine hydrochloride (BENADRYL) and steroids for the events. The outcome of the events was unknown. The reporter considered that the events were related to BNT162B2. Information on the lot/ batch number has been requested.; Sender's Comments: Based on a compatible temporal association and known product safety profile, a causal relationship between events "reaction to it, she had some different allergies and she got severe itching" and BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 0993839
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: tightness in chest, like right side of the chest; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received a dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EJ1685), via an unspecified route of administration on an unspecified date in Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date in Jan2021 (reported as "maybe Saturday or maybe starting Friday"), the patient experienced tightness in chest, like right side of the chest and it still continues this morning. Patient was just wondering if it was just something or if it was a side effect or be anything else. The outcome of the event was not recovered.

Other Meds:

Current Illness:

ID: 0993840
Sex: F
Age:
State: CA

Vax Date: 01/18/2021
Onset Date:
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fever; Chills; This is a spontaneous report from a contactable nurse (reporting for herself). A 49-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1685), via an unspecified route of administration on 18Jan2021 at a SINGLE DOSE for covid-19 immunisation. Medical history included hypertension from an unknown date and unknown if ongoing. Concomitant medication included amlodipine (AMLODIPINE). The patient stated, "I think I am having the side effects, I am having some fever and chills and I had it early yesterday morning." No treatment was received for the events.The outcome of the events was unknown.

Other Meds: AMLODIPINE

Current Illness:

ID: 0993841
Sex: F
Age:
State: IN

Vax Date: 01/15/2021
Onset Date: 01/18/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Developed hives on my torso; Itching; Rash on my legs; This is a spontaneous report from a contactable consumer (patient herself). An 84-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1284 and expiry date not reported), via an unspecified route of administration on 15Jan2021 at single dose for COVID-19 immunisation. Medical history included blood pressure abnormal, Sjogren's which gave her dry skin. The patient was vaccinated at a clinic. Concomitant medications included lisinopril for blood pressure abnormal and furosemide as diuretic for polyuria. On 18Jan2021, the patient developed hives on her torso, itching and rash on her legs. Therapeutic measure was taken as a result of the events that included antihistamine Benadryl. Clinical outcome of the events was not recovered.

Other Meds: LISINOPRIL; FUROSEMIDE

Current Illness:

ID: 0993842
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Episode of like a sleep paralysis; This is a spontaneous report from a contactable nurse (patient). A patient of unspecified age and gender received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date 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. The patient experienced episode of like a sleep paralysis on an unspecified date. Nurse stated, "I am a Nurse, I am going today to get my second, my booster for the Pfizer vaccine. And last time I went to get my booster, they turned me away because I had side effects and I'd told them that. I otherwise felt fine besides having like episode of like a sleep paralysis. And they freaked out and they wanted me to contact you guys to make sure that it is okay. So, they rescheduled me for today. And I send my, I did that online, like my COVID checking thing and I told them about my symptoms but I haven't been contacted by anybody. So, I just wanted to call to be sure before I go for the second COVID Vaccine." The outcome of the event was unknown. Information on the Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0993843
Sex: F
Age:
State: PA

Vax Date: 12/22/2020
Onset Date:
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: low grade fever; myalgia; This is a spontaneous report from a contactable physician (patient). A 35-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number and expiration date were unknown), via an unspecified route of administration on 22Dec2020 at a single dose on left deltoid for COVID-19 immunization. Medical history included asthma exercise induced. There were no concomitant medications. The patient experienced low grade fever and myalgia on unspecified date. Outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0993844
Sex: M
Age:
State: LA

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

Lab Data:

Allergies:

Symptoms: I woke and wasn't feeling good at all; Chills; My throat is little swollen and I have cough; My throat is little swollen and I have cough; This is a spontaneous report from a contactable consumer reporting for himself. A 71-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number/expiration date: not provided), via an unspecified route of administration, on an unknown date as a single dose for COVID-19 IMMUNIZATION. Relevant medical history was none. Concomitant medication was not provided. On an unknown date, the next day after receiving the vaccination, the patient woke up and wasn't feeling good at all and had chills. On an unknown date, the patient reported that his throat was a little swollen and he has a cough. The patient received treatment for the events cough and throat swelling which included ibuprofen and oral septic for his throat. The outcome of the events wasn't feeling good at all and chills was not recovered. The outcome of the events throat is a little swollen and cough was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow-up.

Other Meds:

Current Illness:

ID: 0993845
Sex: F
Age:
State: MI

Vax Date: 01/18/2021
Onset Date: 01/01/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Experiencing like stuffy nose with her sinuses; Developed form of hive on her nose and her sinuses; feel like stuffy head; This is a spontaneous report from a contactable consumer (patient). An 82-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EL3248), via an unspecified route of administration on 18Jan2021 at single dose for covid-19 immunization. The patient medical history was not reported. Concomitant drugs includes levothyroxine sodium which reported as generic for Synthroid. The patient experienced like stuffy nose with her sinuses, developed form of hive on her nose and her sinuses; seems like her sinuses; she felt like stuffy head. The patient wanted to know is that a side effects or a normal reaction. Therapeutic measures were taken as a result of experiencing like stuffy nose with her sinuses includes like Tylenol. The outcome of the events was unknown.

Other Meds: LEVOTHYROXINE SODIUM

Current Illness:

ID: 0993846
Sex: U
Age:
State: TN

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

Lab Data:

Allergies:

Symptoms: Flu like symptoms including chills, fever, night sweats, body aches; Flu like symptoms including chills, fever, night sweats, body aches; Flu like symptoms including chills, fever, night sweats, body aches; Flu like symptoms including chills, fever, night sweats, body aches; Flu like symptoms including chills, fever, night sweats, body aches; This is a spontaneous report from a contactable consumer via Sales Representative. A patient of unspecified age and gender received the second dose 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 medical history was not reported. The patient's concomitant medications were not reported. The patient previously took the first dose BNT162B2 and experienced lot of arm pain. The patient experienced flu like symptoms including chills, fever, night sweats, body aches after 8 hours received vaccine. The outcome of events was unknown. No follow-up attempts are possible, information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0993847
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Contacted Covid after their first vaccine; Contacted Covid after their first vaccine; This is a spontaneous report from a contactable consumer from a Pfizer-sponsored program IBCC (Inbound Call Center for HCPs). This consumer reported similar events for two patients. This is the first of two reports. A patient (reported as: healthcare professional) of unspecified age and gender received the first dose of the bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), 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 experienced: contacted COVID after their first vaccine (medically significant). The clinical outcome of the events, drug ineffective and COVID-19, was unknown. The batch/lot numbers for the vaccine, PFIZER-BIONTECH COVID-19 MRNA VACCINE, were not provided and will be requested during follow up.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021082538 same reporter, drugs and events.; different patient.

Other Meds:

Current Illness:

ID: 0993848
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: On my left arm bothers me it is not a pain that I cannot tolerate but it is lot more than I had first day; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received BNT162B2 (unspecified if Pfizer product), via an unspecified route of administration at left arm in Jan2021 at single dose for COVID-19 immunization. Patient had the vaccine (unspecified vaccine) on Friday on his/her left arm it didn't bother her/him that much very little. patient knew it was there, but nothing happened but after last night patient knew have like it bothers her/him it was not a pain that she/he cannot tolerate but it was lot more than she/he had first day (Jan2021). Patient was taking paracetamol (TYLENOL). Outcome of the event was unknown. Pfizer is a marketing authorization holder of COVID-19 VACCINE in the country of incident or the country where the product was purchased (if different). This may be a duplicate report if another marketing authorization holder of COVID-19 VACCINE has submitted the same report to the regulatory authorities. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0993849
Sex: F
Age:
State: AZ

Vax Date: 01/18/2021
Onset Date: 01/01/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: an excruciating headache; This is a spontaneous from a contactable consumer (patient). This 49-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Batch/lot number: EK9231), via an unspecified route of administration on 18Jan2021 at single dose for COVID-19 immunisation. The patient's medical history included severe chronic migraine. The patient's concomitant medications were not reported. Patient stated she got her second COVID vaccine on 18Jan2021 and she has gotten an excruciating headache in Jan2021. She has taken paracetamol (TYLENOL) and 800 mg ibuprofen on 18Jan2021 and it was actually getting worse. When probed for any treatment for the problem, patient stated yes, her headache, all she had taken for 18Jan2021 so far was paracetamol, diphenhydramine hydrochloride (BENADRYL) (if might have taken for headache) and ibuprofen. Outcome of the event was unknown. No investigation assessment.

Other Meds:

Current Illness:

ID: 0993850
Sex: F
Age:
State: IN

Vax Date: 12/28/2020
Onset Date: 01/08/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data: Test Date: 20210108; Test Name: Covid test; Test Result: Positive ; Test Date: 20210118; Test Name: X-Ray; Result Unstructured Data: Test Result:Unknown Results

Allergies:

Symptoms: tested positive for COVID-19; tested positive for COVID-19; This is a spontaneous report from a contactable consumer, the spouse of the patient. A 62-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL1284), via an unspecified route of administration in the left arm on 28Dec2020 (at the age of 62-years-old) as a single dose for COVID-19 immunization. Medical history included ongoing lupus from an unknown date. Concomitant medications included unspecified medications for her Lupus. On 08Jan2021, the patient tested positive for COVID-19. On 18Jan2021, the patient had an X-ray with unknown results. Therapeutic measures were taken as a result of testing positive for COVID-19 and included an unspecified infusion. The clinical outcome of tested positive for COVID-19 was unknown.

Other Meds:

Current Illness:

ID: 0993851
Sex: F
Age:
State: MN

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

Lab Data:

Allergies:

Symptoms: Right arm, where the vaccine was given, swelled up to the soft ball size; It is a reaction, hardness, warm at the patch, redness and it kept expanding; Right arm, where the vaccine was given, swelled up to the soft ball size; It is a reaction, hardness, warm at the patch, redness and it kept expanding; Right arm, where the vaccine was given, swelled up to the soft ball size; It is a reaction, hardness, warm at the patch, redness and it kept expanding; Right arm, where the vaccine was given, swelled up to the soft ball size; It is a reaction, hardness, warm at the patch, redness and it kept expanding; This is a spontaneous report from a contactable nurse (patient). A 55 years old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL0142/expiration date: MAR-2021) on an unspecified date at single dose via an unspecified route of administration on deltoid Right for COVID-19 immunization. Relevant medical history and concomitant medications were not reported. The patient reported that since an unspecified date right arm, where the vaccine was given, swelled up to the soft ball size; It was a reaction, hardness, warm at the patch, redness and it kept expanding. The patient did not receive treatment for the events. At the time of the reporting events outcome was unknown.

Other Meds:

Current Illness:

ID: 0993852
Sex: M
Age:
State:

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

Lab Data: Test Name: Tested positive after taking the first shot; Test Result: Positive

Allergies:

Symptoms: Tested positive after taking the first shot of the vaccine; Tested positive after taking the first shot of the vaccine; This is a spontaneous report from a Pfizer-sponsored program COVAX US Support. A Non contactable male consumer reported that a male patient of an unspecified age received bnt162b2 (BNT162B2, Covid-19 Vaccine from Pfizer), 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 tested positive after taking the first shot of the vaccine on an unspecified date with outcome of unknown. He wanted to know if he can still take the second dose. He really need to know as he had been scheduled to receive his send dose tomorrow. He really need to know whether to show up or not. The patient underwent lab tests which included sars-cov-2 test: positive on unknown date. No follow up attempts are possible. Information about Lot/ Batch could not be obtained.; Sender's Comments: Based on the information currently available, lack of efficacy of the suspected vaccine BNT162B2 cannot be completely excluded. However, individuals may not be protected until at least 7 days after their second dose of the vaccine. It is unlikely that the patient would have fully developed immunity due to the very short time lag between the first vaccine dose and the event onset.

Other Meds:

Current Illness:

ID: 0993853
Sex: F
Age:
State: IN

Vax Date: 01/11/2021
Onset Date: 01/17/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Developed a vesicular rash; This is a spontaneous report from a contactable Other HCP. A female patient of an unspecified age received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 11Jan2021 at single dose for COVID-19 vaccination. The patient's medical history and concomitant medications were not reported. The patient experienced developed a vesicular rash on 17Jan2021, it was described as 'the patient developed a vesicular rash on day 6. This was the second vaccine. It's not a diffused drug reaction like rash, it's the vesicular'. The outcome of the event was unknown. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0993854
Sex: M
Age:
State: OR

Vax Date: 01/18/2021
Onset Date: 01/19/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Left eye is like somebody hit me on the eye; it is all bruise purple and black all over right between inside the corner of nose of the eye; This is a spontaneous report from a contactable consumer (patient). A 75-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231), via an unspecified route of administration on 18Jan2021 at single dose for COVID-19 immunization. Medical history included cholesterol. The patient was taking cholesterol medication. Nothing special other than what you get when you get older. The patient stated that he woke up this morning (19Jan2021), his left eye was like somebody hit him on the eye. It was not the eye but above the eye. It was all bruise purple and black all over right between inside the corner of nose of the eye and all away cross the top of it. He has no idea that come from. There was no treatment for the event. The outcome of the event was not recovered.

Other Meds:

Current Illness:

ID: 0993855
Sex: F
Age:
State: FL

Vax Date: 01/14/2021
Onset Date: 01/01/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Teeth started chattering in the middle of the night; This is a spontaneous report from a contactable consumer (patient). A 74-year-old female patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 14Jan2021 at single dose for COVID-19 immunization. Medical history reported as none. There were no concomitant medications. The patient experienced teeth started chattering in the middle of the night in Jan2021. The patient did not receive any treatment from event. The outcome of event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0993856
Sex: F
Age:
State: NY

Vax Date: 01/18/2021
Onset Date: 01/18/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Area around her mouth is a little red and it felt itchy; Area around her mouth is a little red and it felt itchy; This is a spontaneous report from a contactable consumer (patient). A 74-year-old female patient 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 18Jan2021 at 09:15, at a single dose, for COVID-19 immunization. The patient had no medical history and concomitant medications. Yesterday morning (18Jan2021) at 9:15, the patient got her vaccine, and around 04:00 PM (also reported as 04:30 PM), yesterday afternoon, the patient started to rub the area around her mouth. And when she looked it in the mirror, it was a little red and it felt itchy. The patient took diphenhydramine hydrochloride (BENADRYL) which helped a little, just one. And the patient put some diphenhydramine hydrochloride topical cream on it also. The patient was able to sleep last night and woke up this morning and the redness is gone. It's not itchy. The patient seemed to be fine, but she doesn't know if it's from the vaccine or not. It's not one of the typical side effects. The patient asked if it is safe for her to get the vaccine (second dose) or if she needs to ask them. The patient's second dose of vaccine is scheduled on 08Feb2021. The patient recovered from the events on 19Jan2021. Information about lot number and expiration date for the suspect product will be requested in follow-up attempts.

Other Meds:

Current Illness:

ID: 0993857
Sex: F
Age:
State: VA

Vax Date: 01/18/2021
Onset Date: 01/01/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: blood pressure; Result Unstructured Data: Test Result:140/100

Allergies:

Symptoms: Body ache; Headache; blood pressure was 140/100; left leg swell; severe pain in toes; feel feverish; Chills; Warm body; This is a spontaneous report from a contactable consumer (patient). A 29-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 18Jan2021 11:00 at single dose for covid-19 immunization. Medical history included asthma. Concomitant medication included salbutamol sulfate (PROVENTIL) for asthma. Patient previously took first dose of bnt162b2 on 30Dec2020 at single dose for covid-19 immunization. Patient got second vaccination on 18Jan2021 and may be around about 11 O'clock on same day patient felt to have a body ache all over which patient knew it was normal. However, it was getting worse throughout the day. And patient couldn't even get up and went to work. Also have very bad headache and patient blood pressure was 140/100. For about 3 hours patient did had left leg swell and caused severe pain in toes, that just subsided. Patient didn't have a fever but patient feel feverish, chills, warm body. Patient had been taking Ibuprofen on and off as treatment. Outcome of events left leg swell and caused severe pain in toes were recovering, and outcome of other events was unknown. Information about Lot/Batch number is requested.

Other Meds: PROVENTIL [SALBUTAMOL SULFATE]

Current Illness:

ID: 0993858
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Allergic reaction; She just looks all daze out; This is a spontaneous report from a contactable consumer reporting for her daughter. A female patient of an unspecified age received a dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number/expiration date: not provided), via an unspecified route of administration, on an unknown date as a single dose for COVID-19 IMMUNIZATION. Relevant medical history was not provided. Concomitant medication included she was on several medications (unspecified medications). On an unknown date, the patient experienced an allergic reaction and she just looks all daze out. The outcome of the events allergic reaction and she just looks all daze out was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow-up.

Other Meds:

Current Illness:

ID: 0993859
Sex: F
Age:
State: GA

Vax Date: 12/23/2020
Onset Date:
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: had some dragging after the first dose; This is a spontaneous report from a contactable other-HCP (Patient) A 56-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EJ1685) on 23Dec2020 at single dose intramuscular in left deltoid for COVID-19 immunization. The patient didn't have relevant medical history or concomitant drugs. Patient reported that she may have had some dragging after the first dose, but it was after the holidays and she was laying around anyway, so if she did, it was not of note to her at the time (as reported). At the time of the reporting event outcome was unknown.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021056967 same patient/drug, different event separated with time

Other Meds:

Current Illness:

ID: 0993860
Sex: F
Age:
State:

Vax Date: 01/17/2021
Onset Date: 01/01/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: soreness at the site, more soreness than after her first shot.; This is a spontaneous report from a contactable consumer reporting for a female patient (nephew's fiance). A female patient of an unspecified age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number/expiration date: not provided), via an unspecified route of administration, on 17Jan2021 as a single dose in the left arm for COVID-19 vaccination. Relevant medical history and concomitant medication were not provided. The patient previously received the first dose of BNT162B2 on 27Dec2020 and experienced soreness at the site, fatigue, and numbness in the left pinky finger (same arm as vaccination). On an unspecified date in Jan2021, the patient experienced soreness at the site, more soreness than after her first shot. The outcome of the event soreness at the site was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow-up.

Other Meds:

Current Illness:

ID: 0993861
Sex: M
Age:
State: TX

Vax Date: 01/06/2021
Onset Date:
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Tightness in right side of my chest; This is a spontaneous report from a contactable consumer (patient). This 48-year-old male patient received a dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EJ1695 or EL1695 and Expiration date 31Mar2021) on 06Jan2021 (at 48 years of age) as single dose for COVID-19 immunisation. Medical history and concomitant medication were not reported. The patient experienced tightness in right side of chest on an unspecified date. Patient called to see if this was a common event as patient was going to the hospital shortly to be sure nothing was wrong. Outcome of event tightness in right side of chest was unknown. The lot number for the vaccine BNT162B2 was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 0993862
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: He felt tired and he said what he had taken; This is a spontaneous report from a contactable consumer. A male patient of an unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry 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. The patient previously received first dose of BNT162B2 for COVID-19 immunization. It was reported that the patient talked about his experience with the first and second doses, and how the second dose affected him a bit more. He did not have a temperature, but he felt tired and he said what he had taken. 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: 0993863
Sex: M
Age:
State:

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: headache; some mild myalgia; This is a spontaneous report from a non-contactable physician (patient). A male patient of an unspecified age received 2nd dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 19Jan2021 at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient was experiencing headache and some mild myalgia post second vaccine administration today (19Jan2021). 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: 0993864
Sex: F
Age:
State: NC

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

Lab Data:

Allergies:

Symptoms: Minor headache; Sore arm; This is a spontaneous report from a contactable Other-HCP. A 43-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number/expiration date unknown) on 08Jan2021 at 15:30 at single dose on left deltoid/arm via an unspecified route of administration for COVID-19 immunization. Patient was instructed by head of infectious DZ Dept hospital to premedicate with Tylenol and Benadryl. On an unspecified date she experienced minor headache and sore arm, without other response to second dose. At the time of the reporting event outcome was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0993865
Sex: U
Age:
State: SD

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

Lab Data:

Allergies:

Symptoms: pericarditis; Initial information regarding an unsolicited valid serious case was received from a other healthcare professional via Agency (Reference number- 00438099) and transmitted to Sanofi on 20-Jan-2021. This case involves patient (unknown demographics) who experienced pericarditis, while he/she received vaccine INFLUENZA USP TRIVAL A-B SUBVIRION VACCINE [FLUZONE]. The patient's medical history, past medical treatment, vaccination, concomitant medication and family history were not provided. On an unknown date, the patient received a dose of suspect INFLUENZA USP TRIVAL A-B SUBVIRION VACCINE (lot number: UH478AC and expiry date not reported) via an unknown route at an unknown administration site for prophylactic vaccination. On an unknown date, the patient developed a serious pericarditis (unknown latency) following the administration of INFLUENZA USP TRIVAL A-B SUBVIRION VACCINE. This event was assessed as medically significant. Laboratory details were not reported. It was not reported if the patient received a corrective treatment. The event outcome was unknown for pericarditis.; Sender's Comments: The patient (unknown demographics) who presented with pericarditis after vaccination with FLUZONE. The time to onset is unknown. Medical history, concomitant medication, lab data ruling out alternative etiologies would be needed for complete assessment of the case. Based upon reported information role of vaccine cannot be assessed.

Other Meds:

Current Illness:

ID: 0993866
Sex: F
Age: 74
State: CA

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies: none

Symptoms: arm pain at injection site & small comma rash at bottom of injection site two weeks later now have red rash area size of baseball no pain

Other Meds: none

Current Illness: none

ID: 0993867
Sex: M
Age: 42
State: IN

Vax Date: 01/30/2021
Onset Date: 01/31/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data: No

Allergies: Penicillin

Symptoms: Achy body chills headache rash on neck

Other Meds: No

Current Illness: No

ID: 0993868
Sex: F
Age: 25
State: CA

Vax Date: 01/04/2021
Onset Date: 01/11/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies: Seasonal allergies

Symptoms: Moderate injection site pain followed by lymphadenopathy

Other Meds: Low-ogestrel, zyrtec

Current Illness:

ID: 0993869
Sex: F
Age: 46
State: NJ

Vax Date: 01/28/2021
Onset Date: 01/29/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data:

Allergies: None

Symptoms: Severe Nausea as well as a sore arm was persistent for 3 days following the injection. In addition, a rash appeared on the left side of my back and left thigh.

Other Meds: None

Current Illness: None

ID: 0993870
Sex: F
Age:
State: IL

Vax Date: 01/25/2021
Onset Date: 01/26/2021
Rec V Date: 02/02/2021
Hospital:

Lab Data: Forced me to get a Covid 19 test and result was NEGATIVE

Allergies: None

Symptoms: Full blown flu symptoms. Fever, aches, cough, head conjestion, exhaustion, memory loss, depression, loss of appetite, diarrhea. Missed 5 days of work

Other Meds: None

Current Illness: None

ID: 0993950
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: Back side of arm has been progressively getting redder; Swollen; Painful; A big raised lump on back of her arm; Thinks she received the vaccine subcutaneously; A spontaneous report was received from a pharmacist concerning a female patient who received Moderna's Covid-19 vaccine (mRNA-1273) and thinks she received the vaccine subcutaneously, back side of arm has been progressively getting redder, swollen, and painful and a big raised lump on back of her arm. The patient's medical history was not provided. Concomitant product use was not provided. On 08 J an 2021 The patient received their first of two planned doses of mRNA-1273 for prophylaxis of COVID-19 infection Lot # 012L20A. On an unknown date the patient's back of arm was progressively getting redder, swollen and painful. The pharmacist stated, "it looks like a big raised lump on back of her arm". Treatment information was not provided. Action taken with mRNA-1273 in response to the events was not provided. The event, thinks she received the vaccine subcutaneously, was considered resolved on 08 Jan 2021. The events, back side of arm has been progressively getting redder, swollen, and painful and a big raised lump on back of her arm, was considered unknown.; Reporter's Comments: This regulatory report concerns a female patient who experienced thinks she received the vaccine subcutaneously (inappropriate route of vaccine administered), back side of arm has been progressively getting redder, swollen, and painful and a big raised lump on back of her arm. The event occurred following the administration of the first dose of the vaccine mRNA-1273 vaccine (Lot #: 012L20A, expiration date-unknown). Treatment administered was not reported and outcome was unknown. Based on the information provided which includes a strong temporal association and the absence of any other etiology, the events of back side of arm has been progressively getting redder, swollen, and painful and a big raised lump on back of her arm, a causal association with the vaccine administration cannot be excluded. The event of inappropriate route of vaccination is considered not applicable.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm