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: 0936645
Sex: F
Age: 34
State: OH

Vax Date: 12/23/2020
Onset Date: 12/23/2020
Rec V Date: 01/12/2021
Hospital:

Lab Data: NA

Allergies: NA

Symptoms: Nausea, vomiting, diarrhea starting at 2230 until 0100. Body aches, chills, fatigue, difficulty concentrating until 12/25 afternoon

Other Meds: Zoloft 100mg daily Implanon implant

Current Illness: None

ID: 0936646
Sex: U
Age:
State: CA

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

Lab Data:

Allergies:

Symptoms: Nurse had the same symptoms but her symptoms were even worse. She had some numbness in the face and the extremities and her symptoms lasted longer and then subsided next day according to the nurse; This is a spontaneous report from a contactable physician. A patient (ICU nurse) of unspecified age and gender received 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's medical history and concomitant medications were not reported. The reporter reported that the nurse had some numbness in the face and the extremities and her symptoms lasted longer and then subsided next day according to the nurse who administered the vaccine to the reporter but again, the reporter didn't know if even those guys were reporting this or not. The outcome of the event was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0936647
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: had covid after his first dose; had covid after his first dose; headaches; This is a spontaneous report from a Pfizer-sponsored program Pfizer First Connect from a contactable Physician. A male patient of an unspecified age received his first single dose of BNT162B2 (Pfizer/ BioNTech Covid-19 vaccine) on an unspecified date in Dec2020 for Covid-19 immunization. The patient previously had Covid in Apr2020. Concomitant medications were not reported. After his first dose of vaccine, in Dec2020, the patient had Covid and headaches. The outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: The reported "had Covid" after COVID-19 immunization is considered ineffective of BNT162B2, and the Company cannot completely exclude the possible causality between the reported event and BNT162B2 administration.

Other Meds:

Current Illness:

ID: 0936648
Sex: F
Age:
State: MI

Vax Date: 12/23/2020
Onset Date: 01/01/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: tested; Result Unstructured Data: Test Result:positive for COVID

Allergies:

Symptoms: Got the first dose of the vaccine on 23Dec2020, this week the patient was tested positive for COVID; Got the first dose of the vaccine on 23Dec2020, this week the patient was tested positive for COVID; This is a spontaneous report from a Pfizer-sponsored program Pfizer First Connect from a contactable other healthcare professional (HCP) (patient). A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 23Dec2020 at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient got the first dose of the vaccine on 23Dec2020, this week the patient was tested positive for COVID in Jan2021. The outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: The reported tested positive for COVID after COVID-19 immunization is considered ineffective of BNT162B2, and the Company cannot completely exclude the possible causality between the reported event and BNT162B2 administration.

Other Meds:

Current Illness:

ID: 0936649
Sex: F
Age:
State:

Vax Date: 12/16/2020
Onset Date:
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Name: she tested positive in the middle; Test Result: Positive

Allergies:

Symptoms: she tested positive in the middle; she tested positive in the middle; This is a spontaneous report from a contactable female consumer (patient) via a Pfizer-sponsored program . A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 16Dec2020 at first single dose for COVID-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. Caller was asking if it was safe for her to get the second dose, she had the 1st dose on the 16Dec2020 and scheduled for the second dose today (reported on 06Jan2021), however she tested positive in the middle. Outcome of the event was unknown. information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0936650
Sex: M
Age:
State: VA

Vax Date: 12/21/2020
Onset Date: 12/28/2020
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Date: 20201228; Test Name: Covid-19; Test Result: Positive

Allergies:

Symptoms: tested positive for Covid-19; tested positive for Covid-19; This is a spontaneous report from a contactable healthcare professional (HCP) reporting for himself via a Pfizer-sponsored program Pfizer First Connect. A male patient of an unspecified age received the first single dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number and expiry date not reported) via an unspecified route of administration on 21Dec2020 for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient was tested positive for COVID-19 on 28Dec2020 and he was wondering if he was still able to receive the second dose of the vaccine. The outcome of the event was unknown. Information on the lot/ batch number has been requested.; Sender's Comments: The reported tested positive for COVID-19 after COVID-19 immunization is considered ineffective of BNT162B2, and the Company cannot completely exclude the possible causality between the reported event and BNT162B2 administration.

Other Meds:

Current Illness:

ID: 0936651
Sex: U
Age:
State: NJ

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

Lab Data:

Allergies:

Symptoms: some arm soreness in the injected arm; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on arm, 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 reported he had already received his first dose of the Pfizer covid-19 vaccine and tolerated it well, but he did experience some arm soreness in the injected arm. The outcome of event was recovered. Information on the Lot/Batch number has been requested

Other Meds:

Current Illness:

ID: 0936652
Sex: F
Age:
State: CA

Vax Date: 01/04/2021
Onset Date: 01/06/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: some rashes on her face; This is a spontaneous report from a Pfizer-sponsored program, from a contactable consumer (patient). A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 04Jan2021 at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient had some rashes on her face on 06Jan2021. She would like to know if it's okay to take diphenhydramine hydrochloride (BENADRYL). The outcome of event was unknown. Information on the lot/batch number has been requested

Other Meds:

Current Illness:

ID: 0936653
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: diarrhea; loss of smell and taste; loss of smell and taste; This is a spontaneous report from a non-contactable pharmacist. A 72-year-old male patient received BNT162B2 (Pfizer/ BioNTech Covid-19 vaccine) at a single dose on an unspecified date for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. After the vaccination, the patient experienced diarrhea and loss of smell and taste. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0936654
Sex: M
Age:
State: TX

Vax Date: 12/31/2020
Onset Date:
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Name: body temperature; Result Unstructured Data: Test Result:fever (unknown value)

Allergies:

Symptoms: I still feel little bit fatigue during the day but nothing compared to the evening hours; Joint pain; Muscle pain; Fever only last about only 2 hours and then it goes away; This is a spontaneous report from a contactable consumer (patient). A 38-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 31Dec2020 at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient reported that: "during the day I feel almost like 80%, I still feel little bit fatigue during the day but nothing compared to the evening hours, in the evening hours and in the early morning, I am getting like severe joint pain, muscle pain and I also come down with fever from last two nights but the fever only last about only 2 hours and then it goes away". The patient outcome of fever was recovered, the outcome of the other events was unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0936655
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Pain; I never had a sinus effect but it feels like stuffy and painful in my nose and running a little bit; I never had a sinus effect but it feels like stuffy and painful in my nose and running a little bit; I never had a sinus effect but it feels like stuffy and painful in my nose and running a little bit; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), Batch/lot number Unknown, 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 reported that was okay for an hour and then suddenly the patient on an unspecified date experienced pain and felt like stuffy and painful in patient nose and running a little bit. The patient was treated with BENADRYL. The outcome of the events was recovering. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0936656
Sex: F
Age:
State: NY

Vax Date: 01/04/2021
Onset Date: 01/01/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: Body temperature; Result Unstructured Data: Test Result:100.1 Fahrenheit

Allergies:

Symptoms: I am running my temperature 100.1; Chills; Body is still painful; my body achy, my back hurts; every joints hurt in me; Body is still painful; my body achy, my back hurts; every joints hurt in me; Body is still painful; my body achy, my back hurts; every joints hurt in me; This is a spontaneous report from a contactable consumer (patient) and a contactable other health professional. A 54-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 04Jan2021 at single dose for COVID-19 immunization. The patient medical history was none. There were no concomitant medications. On Jan2021, the patient reported that: "I am running my temperature 100.1, chills in my body and my body is still painful. I don't have shortness of breath, but I am very painful. I took 2 TYLENOL. I woke with chills, I have my body achy, my back hurts. I am in pain, every joint hurt in me. I took my temperature and I realized it was 100.1". The patient outcome of fever and chills was unknown, the outcome of the other events was not recovered. Information on Lot/Batch has been requested.

Other Meds:

Current Illness:

ID: 0936657
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: I have had since then sleeping disturbances which means I woke several times in the night; I have had since then sleeping disturbances which means I woke several times in the night; This is a spontaneous report from a non-contactable physician who reported for themselves. A patient of unspecified age and unspecified gender received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) via an unspecified route of administration on an unspecified date (at an unspecified age) as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient experienced "I have had since then sleeping disturbances which means I woke several times in the night" on an unspecified date. The patient called and stated that they were a family doctor and had a question about the COVID-19 vaccine. The patient reported that they "got this vaccine about a week ago and I have had since then sleeping disturbances which means I woke several times in the night. The question is if the company has experienced any complaints for it." The patient was informed about the Pfizer Medical Information department and as department was closed the telephone number was provided. The clinical outcome of the event "I have had since then sleeping disturbances which means I woke several times in the night" was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0936658
Sex: M
Age: 42
State: NY

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

Lab Data:

Allergies: Latex allergy. Wheat and dairy.

Symptoms: Peripheral neuropathy. Needles and tingling from finger tips to shoulder - bilateral. More pronounced in left arm where vaccine was administered. Sensation lasted about 30 minutes and then subsequently subsided. No treatment needed. No further symptoms the following day besides injection site soreness.

Other Meds: Rapaflo 8 mg

Current Illness: None

ID: 0936659
Sex: F
Age:
State: CA

Vax Date: 01/04/2021
Onset Date:
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Name: blood work; Result Unstructured Data: Test Result:Unknown result; Test Name: fever; Result Unstructured Data: Test Result:peaked till 100; Test Name: fever; Result Unstructured Data: Test Result:dropped down to 98

Allergies:

Symptoms: Coughing; chills; she is feeling like a headache, might be from all the coughing; she threw up a yellow stuff, I think the yellow mucous or acid; Fever; This is a spontaneous report from a contactable consumer (patient's spouse) via a Pfizer-Sponsored Program, Pfizer First Connect. A 33-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot #: EL1284) via an unspecified route of administration on 04Jan2021 (at the age of 33-years-old) as a single dose for COVID-19 immunization. Medical history was reported as "none". Concomitant medications were not reported. The patient experienced "coughing", "chills", "she is feeling like a headache, might be from all the coughing", "she threw up a yellow stuff, I think the yellow mucous or acid" and "fever", all on unspecified dates. It was reported that "the reporter called concerned about his wife who got the Pfizer BioNTech COVID-19 vaccine "yesterday" and then she started coughing and experienced a fever." The reporter stated "she was coughing a lot and she threw up a yellow stuff, I think the yellow mucous or acid or whatever. She had a fever that peaked till 100. I gave her Aspirin, it dropped down to 98 at the moment, but she was still having chills." The reported stated that "I just gave Aspirin for the fever. She said at the back of her neck you know she said that she is feeling like a headache, might be from all the coughing." The patient underwent lab tests reported as "got blood work for allergies and stuff like that". When inquired regarding the indication, the reporter stated, "she was caring for my uncle who is 65 and older". The reported stated "I feel that it is recovering, it's getting better". The clinical outcome of the event "chills" was not recovered/not resolved whereas the clinical outcomes of the events "coughing", "she is feeling like a headache, might be from all the coughing", "she threw up a yellow stuff, I think the yellow mucous or acid" and "fever" were all unknown.

Other Meds:

Current Illness:

ID: 0936660
Sex: U
Age:
State:

Vax Date: 12/31/2020
Onset Date: 01/04/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Name: Fever; Result Unstructured Data: Test Result:101 Fahrenheit

Allergies:

Symptoms: I just need to lay down I can barely sit up; Headache; I wasn't feeling good; My body is sore; Fever of a 101?F; Diarrhea; I threw up a little bit in the bathroom; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration at single dose on 31Dec2020 for Covid-19 immunisation. Medical history included Covid-19 in Aug2020. Concomitant medications were not reported. The patient stated that, on 04Jan2021 developed headache, I wasn't feeling good, my body is sore, fever of a 101?F, diarrhea, I threw up a little bit in the bathroom. The patient also reported that "I just need to lay down I can barely sit up on an unspecified date. The outcome of events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0936661
Sex: F
Age: 27
State: CA

Vax Date: 01/08/2021
Onset Date: 01/10/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: none

Allergies: none

Symptoms: Itching 2 days after it was given.

Other Meds: none

Current Illness: none

ID: 0936662
Sex: F
Age:
State: AZ

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

Lab Data:

Allergies:

Symptoms: I am having bad rash all over; I started getting in middle in my back and now it just everywhere; This is a spontaneous report from a contactable consumer reporting for herself. A 48-years-old female patient received bnt162b2 ((PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration in the right arm on 03Jan2021 at single dose for COVID-19 immunization. Medical history was none. There were no concomitant medications. The patient experienced bad rash all over; she started getting in middle in her back and now it just everywhere on 03Jan2021 shortly after vaccination with outcome of unknown. The patient was doing anti-histamine and hydrocortisone cream as treatment. Information on the Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 0936663
Sex: F
Age:
State: NC

Vax Date: 12/22/2020
Onset Date: 12/22/2020
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Hives; Itching like a crazy person; This is a spontaneous report from a contactable other health professional (Nurse Practitioner). A 39-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EK5730), intramuscular on 22Dec2020 at single dose on left arm for COVID-19 immunization. Medical history included heavy (Other medical conditions: Consumer stated, "No, I'm healthy other than being a little heavy"). There were no concomitant medications. Patient stated, "I filled out the 'app' after I got my Pfizer Vaccine the first one on 22Dec (Clarification Unknown) but I believe that I have been having a reaction to the vaccination and wanted some kind of guidance on moving forward with the booster and kind of what I should do?" The patient experienced hives and itching like a crazy person when she got the vaccine, 22Dec2020. Treatment in response to treatment, patient stated, "I have taken a lot. It's hives and itching like a crazy person. So I have been take Ibuprofen, and antihistamines like Claritin, Zyrtec and Benadryl." The outcome of the events was recovering ("I would say may be persistent, may be slight improvement"). The events were related to suspect drug as per reporter.

Other Meds:

Current Illness:

ID: 0936664
Sex: U
Age:
State:

Vax Date: 01/04/2021
Onset Date: 01/01/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Bad fever; Body ache; can't get up with arm, really sore; really not feeling good; This is a spontaneous report from a contactable consumer (patient). A patient of an unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: EL0140), via an unspecified route of administration, on 04Jan2021 as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. In Jan2021, the patient experienced bad fever, body ache, can't get up with arm, really sore, and really not feeling good. The clinical outcome of bad fever, body ache, can't get up with arm, really sore, and really not feeling good was unknown.

Other Meds:

Current Illness:

ID: 0936665
Sex: F
Age: 71
State: TX

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

Lab Data:

Allergies: none

Symptoms: MODERNA COVID-19 VACCINE EUA After the vaccine felt sleepy all day but could conduct my daily life. Left arm became sore during the night. Heartburn during the night, had trouble sleeping due to heartburn. Heartburn was stronger than my usual GERD.

Other Meds: Levoxyl

Current Illness: hypothyroidism, GERD

ID: 0936666
Sex: F
Age:
State: IL

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

Lab Data:

Allergies:

Symptoms: Anaphylactic reaction; Flushed; Diaphoretic; redness and rash; hives on chest; Tachycardia; shortness of breath; Chest tightness; Dizziness; Headache; This is a spontaneous report from a contactable nurse, the patient. A 47-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EL1283), via an unspecified route of administration on 08Jan2021 at 08:49 (at the age of 47-years-old) as a single dose for COVID-19 immunization. There were no known medical history or concomitant medications. The patient previously received the first dose of BNT162B2 on 18Dec2020 (Lot Number: EK5730) for COVID-19 immunization and experienced nausea, headache, and fatigue. On 08Jan2021, about 5-10 minutes after the second dose, the patient experienced anaphylactic reaction, flushed, diaphoretic, redness and rash, hives on chest, tachycardia, shortness of breath, and chest tightness, reported as life-threatening. She reported that these events occurred within less than 10 minutes of receiving the vaccine. She went to the emergency room and was treated with methylprednisolone (SOLUMEDROL), diphenhydramine hydrochloride (BENADRYL), famotidine (PEPCID), and epinephrine (MANUFACTURER UNKNOWN). She was sent home and prescribed methylprednisolone and epinephrine (EPI-PEN). Later on 08Jan2021, she experienced dizziness and headache, which were consistent. She stated she would most likely take ibuprofen (MOTRIN) as treatment (not specified if taken). The clinical outcomes of the flushed, diaphoretic, redness and rash, hives on chest, tachycardia, shortness of breath, and chest tightness were recovered on 08Jan2021; while the outcomes of the dizziness and headache were not recovered and that of the anaphylaxis was reported as recovering.; Sender's Comments: The reported information is limited. Based on the close temporal relationship and the description of the events, there is a reasonable possibility that the events are related to BNT162 vaccine. 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: 0936667
Sex: F
Age:
State: LA

Vax Date: 12/29/2020
Onset Date:
Rec V Date: 01/12/2021
Hospital:

Lab Data: Test Name: Lab work; Result Unstructured Data: Test Result:unknown results

Allergies:

Symptoms: Head hurting really bad; Bad muscle pain all across shoulder and neck; Bad muscle pain all across shoulder and neck; some other joint pain too; This is a spontaneous report from a contactable consumer, regarding the reporter's mother. An 89-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: EL0140; Expiration date: 31Mar2021), via an unspecified route of administration, on 29Dec2020 (at the age of 89-years-old) at a single dose for COVID-19 immunization. Medical history included blood pressure, heart problems, back issues, hip issues, and kidney problems. The patient's concomitant medications were not reported. The patient experienced head hurting really bad, bad muscle pain all across shoulder and neck, and some other joint pain too on an unspecified date. The clinical course was reported as follows: The reporter called regarding their mother, who was vaccinated on 29Dec2020. The patient's head was hurting really bad, which she never has a headache and was having bad muscle pain all across her shoulder and neck. The patient was given paracetamol (TYLENOL ARTHRITIS) 650 mg and heat pad. She was having some other joint pain too and the fever was fine. The patient underwent lab tests and procedures which included lab work: unknown results on an unspecified date. Therapeutic measures were taken as a result of the events as aforementioned. The clinical outcome of head hurting really bad, bad muscle pain all across shoulder and neck, and some other joint pain too was unknown. The batch/lot number for the vaccine, BNT162B2, was provided, but will be confirmed/requested during follow up.

Other Meds:

Current Illness:

ID: 0936668
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: glands in throat really swollen; muscles in right leg started spasming; This is a spontaneous report from a contactable consumer (patient). A patient of an unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, on an unspecified date as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced glands in throat really swollen and muscles in right leg started spasming on an unspecified date. The clinical course was reported as: The patient received the vaccine and woke up with glands really swollen and, in the evening, muscles in legs started spasming in right leg. The muscle spasms persisted over the last day or so. The clinical outcome of glands in throat really swollen and muscles in right leg started spasming was unknown. The batch/lot number for the vaccine, BNT162B2, was not provided and has been requested during follow up.

Other Meds:

Current Illness:

ID: 0936669
Sex: F
Age: 33
State: OR

Vax Date: 12/31/2020
Onset Date: 01/09/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: none.

Allergies: penicillin

Symptoms: Injection site swelled , was sore, became itchy, and was hot to the touch. It began the evening of 1/8/21 as tenderness and itchy but increased in size, temperature, and increased tenderness and itch the evening of 1/9/21. I took 3 ibuprofen and iced for 30 minutes. By morning, swelling was down and not as sore. Site still remains itchy at times.

Other Meds: Metformin, concerta, lamotragine, wellbutrin, omega 3 vitamin, vitamin D, melatonin, Solifenacin?

Current Illness: n/a

ID: 0936670
Sex: F
Age:
State: AL

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

Lab Data:

Allergies:

Symptoms: when they put the vaccine into the patient's deltoid, it helped the patient's shoulder have more range of motion just a little bit; when they put the vaccine into the patient's deltoid, it helped the patient's shoulder have more range of motion just a little bit; This is a spontaneous report from a contactable consumer (EMT, Emergency Medical Technician). A 59-year-old female patient received the bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot Number and Expiration Date: unknown), via an unspecified route of administration in the deltoid on 30Dec2020 at 59-years-old at a single dose for COVID-19 immunization. Medical history included bad shoulder from an unknown date and unknown if ongoing. Concomitant medications included vitamins from an unspecified date to an unspecified date. On an unspecified date, the patient experienced: when they put the vaccine into the patient's deltoid, it helped the patient's shoulder have more range of motion just a little bit. The clinical course was reported as follows: The patient stated, "so everybody is talking about the negative, the adverse reactions, but I would like to perhaps report a positive reaction." The patient had a bad shoulder for 10 or 15 years. The administrating professional put the vaccine into the patient's deltoid ("my shoulder muscle"). The patient stated, "I don't know, maybe it helped my shoulder have more range of motion just a little bit." The clinical outcome of the events: unexpected therapeutic effect and pre-existing condition improved, was unknown. No follow-up attempts are needed; information about batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 0936671
Sex: M
Age:
State: TX

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

Lab Data:

Allergies:

Symptoms: dizziness; This is a spontaneous report from a contactable consumer (patient 's wife). A male patient of unknown age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, on 03Jan2021 at single dose for COVID-19 immunisation. Medical history and concomitant medications were unknown. The patient was having some issues, he says he keeps getting dizziness. Outcome is unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0936672
Sex: F
Age:
State: PA

Vax Date: 01/03/2021
Onset Date: 01/04/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chills; Fever; Body ache; This is a spontaneous report from a contactable consumer, the patient. A 44-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on 03Jan2021 (at the age of 44-year-old) as a single dose for COVID-19 immunization. Medical history included already tested positive for COVID. There were no concomitant medications. On 04Jan2021 the patient experienced chills, fever, and body ache. Therapeutic measures taken as a result of chills, fever, and body ache included Tylenol 500 mg. The clinical outcome of the events chills, fever, and body ache was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 0936673
Sex: F
Age: 32
State: IN

Vax Date: 01/09/2021
Onset Date: 01/09/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: N/a

Allergies: NKA

Symptoms: Twelve hours after dose: headache, diarrhea, myalgia, cervical lymphadenopathy, nausea, fatigue. Side effects improved by 48 hours after injection and completely resolved by 72 hours after injection.

Other Meds: Unithroid Vitamin c Prenatal vitamin Aleve

Current Illness: N/A

ID: 0936675
Sex: U
Age:
State: VA

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

Lab Data:

Allergies:

Symptoms: a VAQTA vaccine which had been improperly stored was administered to a patient.; This spontaneous report was received from a medical assistant referring to a patient of unknown age and gender. Information about medical history, concurrent conditions and concomitant therapies was not provided. On 28-DEC-2020, the patient was vaccinated with improperly stored hepatitis a vaccine, inactivated(VAQTA) (lot # T013204, expiration date 03-DEC-2021, 1 injection) for prophylaxis (product storage error). The temperature excursion was supported, at below 36 Fahrenheit degree (32.1 Fahrenheit degree) for 5 hours and 40 minutes. There were no previous excursions, and a data logger was used. combinationproductreport: Yes; brandname: VAQTA SYRINGE (DEVICE); commondevicename: Hepatitis A Vaccine, Inactivated; productcode: FMF; devicetype: SYRINGE, PISTON (FMF); manufacturername: Merck Sharp & Dohme Corp.; devicelotnumber: T013204; expirationdate: 03-DEC-2021; deviceage and unit: 0 ; malfunction: Unknown; deviceusage: Initial; reasonfornoneval: 81 Other; labeledsingleusedevice: No; mdcpreportability: No; mdcpreprationale: Case information does not meet the criteria for Reportability

Other Meds: VAQTA SYRINGE (DEVICE)

Current Illness:

ID: 0936676
Sex: F
Age: 67
State: PA

Vax Date: 09/11/2020
Onset Date: 11/24/2020
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: arm sore / pain in right arm; weakness in right arm; Today patient was in a lot of pain / worse during lateral movements or / raises her arm above her head; weakness are worse during lateral movements / raises her arm above her head; right arm was hot for 3 days; This case was reported by a consumer via call center representative and described the occurrence of pain in arm in a 67-year-old female patient who received Herpes zoster (Shingrix) (batch number MT7C9, expiry date unknown) for prophylaxis. Co-suspect products included Flu Seasonal QIV Dresden (Influenza vaccine Quadrivalent 2020-2021 season) for prophylaxis. Previously administered products included Pneumonia vaccine (got last year). Concurrent medical conditions included ileo-anal pouch (J pouch) and colon cancer. On 11th September 2020, the patient received the 1st dose of Shingrix and Influenza vaccine Quadrivalent 2020-2021 season. On 24th November 2020, 74 days after receiving Shingrix and Influenza vaccine Quadrivalent 2020-2021 season, the patient experienced pain and weakness. On an unknown date, the patient experienced pain in arm, weakness of arms and extremities hot feeling of. On an unknown date, the outcome of the pain in arm and weakness of arms were not recovered/not resolved and the outcome of the extremities hot feeling of was recovered/resolved and the outcome of the pain and weakness were unknown. It was unknown if the reporter considered the pain in arm, weakness of arms, extremities hot feeling of, pain and weakness to be related to Shingrix. It was unknown if the reporter considered the pain and weakness to be related to Influenza vaccine Quadrivalent 2020-2021 season. Additional details were provided as follows: The patient received 1st dose of Shingrix in her right arm deltoid and a flu shot at the same time in her left arm deltoid. The patient reported right arm sore and hot for 3 days then resolved. The patient reported continued weakness and pain in right arm. The patient does arm exercise reps at the gym with 10 to 12 pound weights and did so last night. On 24th November 2020, the patient was in a lot of pain. The patient stated that the pain and weakness were worse during lateral movements or when she raises her arm above her head. The reporter did not consented to follow up.

Other Meds:

Current Illness: Colon cancer; Ileo-anal pouch (J pouch)

ID: 0936677
Sex: M
Age:
State: NJ

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

Lab Data:

Allergies:

Symptoms: Neuropathy / is going to receive Shingrix?s 2nd dose; This case was reported by a pharmacist via call center representative and described the occurrence of neuropathy in a elderly male patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the patient received the 1st dose of Shingrix. On an unknown date, unknown after receiving Shingrix, the patient experienced neuropathy (serious criteria GSK medically significant). The patient was treated with immunoglobulin human normal (Gammagard). On an unknown date, the outcome of the neuropathy was not recovered/not resolved. It was unknown if the reporter considered the neuropathy to be related to Shingrix. Additional information was provided as follows: The reporter stated that a patient who was currently receiving Gammagard because of a neuropathy and the patient was going to receive Shingrix 2nd dose. No other information about the patient?s medical condition was provided and did not have any vaccine information. The reporter consented to follow up. No further information was available.

Other Meds:

Current Illness:

ID: 0936678
Sex: F
Age: 69
State: FL

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

Lab Data: None

Allergies: Seafood

Symptoms: After the vaccine was administered, she decided to check her pulse and see that was a little high, get scared. She was evaluated by the Fire Rescue at 10:30 am and was released home at 10:45 am.

Other Meds: Synthroid, cabapin, glinepinile, gymnema

Current Illness: Diabetic, thyroid

ID: 0936679
Sex: F
Age: 48
State: WA

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 01/12/2021
Hospital:

Lab Data: none

Allergies: no

Symptoms: Large local red rash at the injection site. Hot to the touch, very itchy. Applied cortisone topical and took PO Benadryl for a few days. The rash started to improve after three days of taking Benadryl.

Other Meds: Multivitamin, Vitamin C, Vitamin D, calcium

Current Illness: none

ID: 0936680
Sex: F
Age: 29
State: MI

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

Lab Data:

Allergies: Aspirin

Symptoms: Nausea Body aches Fatigue Headache Injection site soreness

Other Meds: Larin and sertraline

Current Illness: None

ID: 0936681
Sex: F
Age: 23
State: MA

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

Lab Data:

Allergies: past severe adverse reaction to flu vaccine, silver

Symptoms: Muscle soreness in left arm, fever at 99.6 degrees starting 6 hours after injection. Fever went to 100.5 degrees at 1am, 11 hours after injection, and stayed at over 100 degrees until 6:30am, (100.4) when I took Tylenol as recommended by the nurse who administered the injection.

Other Meds: topimax 50mg once daily, daily fiber supplement

Current Illness:

ID: 0936682
Sex: F
Age: 42
State: KY

Vax Date: 12/22/2020
Onset Date: 12/22/2020
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies: Morphine, Demerol, Percocet, steri-strips, mold, seasonal allergies

Symptoms: Headache, nausea, vomiting, dizziness, body aches, pain at injection site, chills,fatigue

Other Meds: Valtrex

Current Illness:

ID: 0936683
Sex: F
Age: 66
State: TX

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: None needed.

Allergies: Nystatin

Symptoms: I felt close to passing out as my first symptom after receiving the booster. Since I had not heard this as a reaction, I thought I should report it. I felt faint numerous times up to 90 hours afterward. Then complete resolution. I also had 101 fever for 24 hours, chills, body aches, but these symptoms have been listed as common.

Other Meds: Telmesartan 80mg, Bystolic 5mg, Plavix 75mg,

Current Illness: None acute.

ID: 0936684
Sex: F
Age: 26
State: AR

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

Lab Data: N/A

Allergies: NKA

Symptoms: Muscle/joint aches, low grade fever, chills happens every 4 hours.

Other Meds: N/A

Current Illness: N/A

ID: 0936685
Sex: M
Age: 86
State: FL

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

Lab Data: None

Allergies: Penicillin

Symptoms: After the vaccine, the wife verbalized her husband felt lightheaded and dizzy. He was evaluated by Fire Rescue and released home at 2:32 pm.

Other Meds: Dioban

Current Illness: HBP

ID: 0936686
Sex: M
Age: 22
State: WI

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

Lab Data: N/A

Allergies: None

Symptoms: I developed headache, low grade fever, and nausea at approximately 11:59 PM 1/11/2021. As of 05:42 AM 1/12/2021 these symptoms persist. Headache reduced via ibuprofen, fever and nausea did not respond.

Other Meds: None

Current Illness: None

ID: 0936687
Sex: F
Age: 44
State: NH

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

Lab Data: None

Allergies: None

Symptoms: Uncontrollable chills, achiness, headache, nightmares

Other Meds: None

Current Illness: None

ID: 0936688
Sex: F
Age: 42
State: MS

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

Lab Data:

Allergies: None

Symptoms: Nausea, headache, vomiting, chills, body aches, pain at injection, dizzy

Other Meds: Aimovig 140 injection 1/month Imitrex 100 mg prn Levothyroxine 88mcg Hydroxide B12, folinic acid, magnesium

Current Illness: None

ID: 0936689
Sex: F
Age: 65
State: WI

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

Lab Data:

Allergies:

Symptoms: I had body aches, headaches, and just felt tired. I took Tylenol extra strength every 6 hours for a 24 hour period. After that I felt fine.

Other Meds:

Current Illness:

ID: 0936690
Sex: M
Age: 41
State: FL

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

Lab Data:

Allergies: Pcn, shellfish

Symptoms: Fever, shortness of breath, nausea

Other Meds: Locinopril 5mg

Current Illness: None

ID: 0936694
Sex: F
Age: 75
State: MN

Vax Date: 10/19/2020
Onset Date: 10/20/2020
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Can barely move her arm / Difficult to raise her arm; Cannot sleep at night because of the pain; quite painful / aches at night/SORENESS IN THE LEFT ARM/Soreness in the left arm / "it puts me over the floor"; Swollen in the arm muscle halfway between the elbow and shoulder; This case was reported by a pharmacist via call center representative and described the occurrence of pain in arm in a 75-year-old female patient who received Herpes zoster (Shingrix) for prophylaxis. On 19th October 2020, the patient received the 1st dose of Shingrix. On 20th October 2020, 1 days after receiving Shingrix, the patient experienced pain in arm and swelling arm. On an unknown date, the patient experienced injected limb mobility decreased and sleeplessness. The patient was treated with analgesic, nos (Pain Medication). On an unknown date, the outcome of the pain in arm, injected limb mobility decreased, swelling arm and sleeplessness were not recovered/not resolved. It was unknown if the reporter considered the pain in arm, injected limb mobility decreased, swelling arm and sleeplessness to be related to Shingrix. Additional details were provided as follows: The patient received 1st dose pretty high in her left arm. The patient stated that the lot number and expiration date of vaccine were not available. The patient experienced soreness in the left arm and difficult to raise her arm. The patient still had swelling, aches at night and could barely move her arm (moving her arm would cause it to ache more). The patient reported, she could not sleep at night because of the pain and it puts her over the floor. The patient described that the pain was not at the injection site and it was swollen in the arm muscle halfway between the elbow and shoulder of the left arm. The patient reported a pain medication was prescribed but it did not help at all and the pain has not resolved. The patient gave permission to follow up with her doctor. This case had been linked with US2020231854, reported by the same reporter.; Sender's Comments: US-GLAXOSMITHKLINE-US2020231854:same reporter US-GLAXOSMITHKLINE-US2020239794:Same reporter. From FU1 deleted

Other Meds:

Current Illness:

ID: 0936695
Sex: F
Age:
State: TX

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

Lab Data:

Allergies:

Symptoms: anaphylactic reaction to an influenza vaccine; Initial information regarding an unsolicited valid serious case was received from a consumer/non-health care professional (Reference number- 00416355) and transmitted to Sanofi on 05-Jan-2021. This case involves female patient of an unknown age who experienced anaphylactic reaction, while she received INFLUENZA VACCINE. Medical history, medical treatment, concomitant medication, vaccination and family history were not provided. On an unknown date, the patient received a dose of suspect INFLUENZA VACCINE produced by unknown manufacturer (lot number 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 anaphylactic reaction, (unknown latency) following the administration of INFLUENZA VACCINE. This event was assessed as medically significant. Reporter was told that the reaction was due to the egg content and informed about components of Flublok. Details of laboratory data not reported. It was not reported if the patient received a corrective treatment. At the time of reporting, the outcome of event was reported as unknown. Information on the batch number was requested.; Sender's Comments: This case concerns female patient of an unknown age who had anaphylactic reaction, after vaccination with INFLUENZA VACCINE (unknown manufacturer). The time to onset is unknown. The patent has a history of egg allergy. Additional information regarding patient's medical history, condition at the time of vaccination, lab data excluding other etiologies would be needed for complete assessment of the case. Based upon the reported information, the role of the vaccine cannot be assessed.

Other Meds:

Current Illness:

ID: 0936696
Sex: F
Age: 39
State: FL

Vax Date: 01/04/2021
Onset Date: 01/11/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data:

Allergies: Latex

Symptoms: I have a mark from the vaccine i got as a child. I think its a smallpox which i received at birth in 1981. Only around and on that prior vaccination site is a little swollen and very red. It itches a lot. It is raised and red. My vaccination was 2-4 cm cephalad to the mark. I was ok until Monday morning a week later woke up with it. Felt fatigued and achy all day following the next day. Today, 1/12/21, it is still red with a ring around the prior vaccination and fatigue to follow.

Other Meds: Birth Control and Melatonin

Current Illness:

ID: 0936697
Sex: F
Age: 44
State: PA

Vax Date: 01/05/2021
Onset Date: 01/12/2021
Rec V Date: 01/12/2021
Hospital:

Lab Data: none

Allergies: NKDA

Symptoms: On January 6,2021 when I woke up my face was red, swollen and extremely warm. My face was like this for at least 16 hours (very uncomfortable). Also, on January 6, 2021 at 1130pm I had horrible stomach pains, then started vomiting, after I was done vomiting I felt better. I did take 2 Benadryl and aleve to help When I got back injections and had surgeries I had the same reactions happen to me usually after 8-10 hours after I was out of surgery. I was given medicine to help with the discomfort either through IV or Benadryl.

Other Meds: Plaquenil 200 mg 1 a day Levothyroxine 75mcg 1 a day

Current Illness: n/a

ID: 0936698
Sex: F
Age: 42
State: NC

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

Lab Data:

Allergies: Aveloc

Symptoms: Chest pain, injection site pain, joint pain, nausea vomiting, hot sensation. Generalized fatigue

Other Meds: Site pain. Arm redness. Joint pain all over. Neck pain. Nausea. Hot flashes. Generalized fatigue.

Current Illness: None

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm