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: 0954505
Sex: M
Age:
State: CA

Vax Date: 01/05/2021
Onset Date: 01/05/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: Test Name: body temperature; Result Unstructured Data: Test Result:99.6; Test Date: 20210107; Test Name: body temperature; Result Unstructured Data: Test Result:101

Allergies:

Symptoms: fever of 101; Chills; loose watery stool; stomach problems; threw up a couple of times; headache; Nausea; This is a spontaneous report from a contactable consumer. A 61-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EH9899), via an unspecified route of administration on 05Jan2021 at a single dose (with a syringe left shoulder once; as reported) for Covid protection. Medical history was reported as none. There were no concomitant medications. It was reported that the patient experienced side effects on first Pfizer Covid injection that he had. He got it on Tuesday, 05Jan2021, and got a headache and nausea which started Tuesday evening. His temperature is 99.6. On Thursday, 07Jan2021, he had a fever of 101, nausea, chills, loose watery stool, stomach problems and threw up a couple times. He was under a blanket for the chills all day. His lasting effects was that he still has watery loose stool and went to the bathroom an hour ago. He took Tylenol for fever. He took Immodium yesterday three tablets and woke up at 3-3:30 am and took a couple (also reported as started taking it at 11am then took some at 4am and then two this morning) then some Tylenol. He was still feverish and has loose stools. The patient underwent lab tests and procedures which included body temperature: 99.6 on an unspecified date and 101 on 07Jan2021. The outcome of the events headache, nausea and loose watery stool was not recovered; the events fever of 101 and chills was recovering; and the event threw up a couple of times was resolved on 07Jan2021; while the outcome of all other events was unknown.

Other Meds:

Current Illness:

ID: 0954506
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: arm is sore; This is a spontaneous report from a non-contactable consumer. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The reporter is a Pfizer employee and her daughter's physical therapist mentioned to her that she got the Pfizer vaccine and her arm was sore. 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: 0954507
Sex: F
Age: 60
State:

Vax Date: 01/16/2021
Onset Date: 01/16/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: None

Allergies: Egg white

Symptoms: Watery eyes, runny nose

Other Meds: Amlodipine 7.5mg

Current Illness: None

ID: 0954508
Sex: F
Age:
State: VT

Vax Date: 01/05/2021
Onset Date: 01/09/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: Test Date: 20210104; Test Name: Covid Nasal Swab Test; Test Result: Negative

Allergies:

Symptoms: vomiting; chills; severe headache; stomach pain x72 hrs; severe nausea; dizziness; low blood pressure; This is a spontaneous report from a contactable healthcare professional. A 48-year-old female patient started to receive bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular from 05Jan2021 10:00 to 05Jan2021 10:00 at a single dose for COVID-19. Medical history included asthma, sibo, allergies to wheat, gluten, corn, tomato and peanuts. The patient's concomitant medications were not reported. It was reported that the patient's initial response to shot was severe nausea and dizziness, low blood pressure lasted 24hrs on 09Jan2021. 5 days later, the patient had nausea, vomiting, chills after meal, severe headache and stomach pain 72 hrs. The patient received IV fluids as treatment for all events. The patient underwent lab tests and procedures which included Covid Nasal Swab Test on 04Jan2021 which tested negative. The outcome of the events was not recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0954509
Sex: F
Age: 52
State: UT

Vax Date: 01/14/2021
Onset Date: 01/15/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: None

Allergies: NONE

Symptoms: Chills really bad, had 10 blankets on me, just to get warm. Shivered so bad I looked like I was having a seizure. Lasted about 5 hours. Dull headache for 2 days.

Other Meds: NONE

Current Illness: None

ID: 0954510
Sex: F
Age:
State: IL

Vax Date: 01/07/2021
Onset Date: 01/09/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data:

Allergies:

Symptoms: General fatigue; Joint pain (specifically isolated to my bilateral hands, fingers, thumbs) caused difficulty with gripping objects; This is a spontaneous report from a non-contactable nurse (patient). A 27-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL1283), via an unspecified route of administration on 07Jan2021 17:15 at a single dose on Left arm for COVID-19 immunization. Medical history included depression, anxiety, chronic sinusitis, and allergy seasonal /pet dander. Concomitant medication included venlafaxine hydrochloride (EFFEXOR), bupropion hydrochloride (WELLBUTRIN), asa (ASA), montelukast sodium (SINGULAIR), fexofenadine hydrochloride (ALLEGRA). The patient previously took Ceclor, Sudafed and experienced drug allergies. The patient took the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK5730), via an unspecified route of administration on 17Dec2020 18:15 at a single dose on Left arm for COVID-19 immunization. The patient experienced general fatigue and joint pain ("specifically isolated to my bilateral hands, fingers, thumbs") caused difficulty with gripping objects on 09Jan2021 13:00 ("01:00 PM"). No treatment received for events. The outcome of the events was recovering. The events were assessed as non-serious. The patient was not pregnant at the time of vaccination. Facility where the most recent COVID-19 vaccine was administered was Hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Treatment not received for the adverse event. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Other Meds: EFFEXOR; WELLBUTRIN; ASA; SINGULAIR; ALLEGRA

Current Illness:

ID: 0954511
Sex: F
Age:
State:

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

Lab Data: Test Name: covid Test; Test Result: Positive

Allergies:

Symptoms: tested positive for covid; tested positive for covid; This is a spontaneous report from a contactable consumer (patient) via a Pfizer sponsored program Pfizer Connect. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date not reported), 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 patient works for a hospital. Said had 1st dose of vaccine. Had tested positive for covid on an unspecified date and is under quarantine. The patient would like to know when she should get 2nd dose. The patient underwent lab tests and procedures which included sars-cov-2 test: positive on an unspecified date. The outcome of the events was unknown. Information on the lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0954512
Sex: U
Age:
State: SC

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

Lab Data: Test Name: COVID; Test Result: Positive

Allergies:

Symptoms: got sick and tested positive with COVID; got sick and tested positive with COVID; This is a spontaneous report from a contactable consumer via Pfizer Sponsored Pfizer First Connect. A contactable consumer reported similar events for four patients. This is second of four reports. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot and expiration date unknown), via an unspecified route of administration on an unspecified date at a single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. It was reported that the patient got sick and tested positive with covid on an unspecified date. It was further reported that patient who received the COVID vaccine, tested positive for COVID, and experienced side effects afterwards. The outcome of the events was unknown. Information about batch/lot number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021013589 same drug, similar events, different patient

Other Meds:

Current Illness:

ID: 0954513
Sex: F
Age: 35
State: MD

Vax Date: 01/05/2021
Onset Date: 01/05/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: None

Allergies: Nka

Symptoms: Approximately two hours after the shot, I started feeling very dizzy, I felt off balance and felt as if I will fall while walking, had diarrhea, felt heavy at the back of my head and had neck pains. Had small bout of vertigo when I laid in the bed. Felt very tired and had some brain fog. S/S improved in 12 hours. Should I take the 2nd dose?

Other Meds: None

Current Illness: None

ID: 0954514
Sex: U
Age:
State: SC

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

Lab Data: Test Name: Covid; Test Result: Positive

Allergies:

Symptoms: got sick and tested positive with COVID; got sick and tested positive with COVID; This is a spontaneous report from a contactable consumer via Pfizer Sponsored Pfizer First Connect. A contactable consumer reported similar events for four patients. This is fourth of four reports. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot and expiration date unknown), via an unspecified route of administration on an unspecified date at a single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient got sick and tested positive with covid on an unspecified date and experienced side effects afterwards. The outcome of the events was unknown. Information about batch/lot number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021013589 same drug, similar events, different patient

Other Meds:

Current Illness:

ID: 0954515
Sex: U
Age:
State: SC

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

Lab Data: Test Name: COVID; Result Unstructured Data: Test Result:Positive

Allergies:

Symptoms: got sick and tested positive with COVID after getting the first dose of the COVID vaccine; got sick and tested positive with COVID after getting the first dose of the COVID vaccine; This is a spontaneous report from a contactable consumer received from Pfizer-sponsored program Pfizer First Connect. This consumer reported similar events for four patients. This is 3rd of four reports. A patient of unspecified age and gender received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, 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 got sick and tested positive with COVID after getting the first dose of the COVID vaccine. The outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021013589 same reporter, same product, similar events, different patient.

Other Meds:

Current Illness:

ID: 0954516
Sex: F
Age: 55
State: PA

Vax Date: 01/11/2021
Onset Date: 01/13/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data:

Allergies: Benadryl

Symptoms: Morbilliform rash and itch; no itch, though pt was on Allegra at time of rash development

Other Meds: Bactrim, Nexium, Sucralfate, Allegra

Current Illness: Chronic Gastritis

ID: 0954517
Sex: U
Age:
State:

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: Test Date: 20210108; Test Name: Body temperature; Result Unstructured Data: Test Result:102; Test Date: 20210108; Test Name: Body temperature; Result Unstructured Data: Test Result:103; Test Date: 20210109; Test Name: Body temperature; Result Unstructured Data: Test Result:102.3

Allergies:

Symptoms: fever at around 9 PM 102/ fever it was high as 103/ currently 102.3; anxiety; panic attacks; feeling sick; puked twice; 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 on 08Jan2021 08:00 at single dose for COVID-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient stated, "So I had the vaccine yesterday at 8 AM and I started having symptoms, side effects at about 6 PM. I started having fever at around 9 PM 102, I can't break my fever it was high as 103, my fever is currently 102.3. I am feeling sick, have puked twice now. Once I feel because I had anxiety, panic attacks and then I tried to get my phenergan and puked that up." Outcome of fever was not recovered, other events was unknown.

Other Meds:

Current Illness:

ID: 0954518
Sex: F
Age:
State: MO

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: Test Date: 20210107; Test Name: Covid nasal swab; Test Result: Negative ; Test Date: 20210107; Test Name: Rapid Covid test; Result Unstructured Data: Test Result:Negative

Allergies:

Symptoms: Left arms swollen lymph nodes; runny nose; sore throat; headache; fatigue; This is a spontaneous report from a contactable healthcare professional (patient). A 36-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date were not reported), via an unspecified route of administration on 06Jan2021 12:00 at a single dose in the left arm for COVID-19. Medical history included asthma, seasonal allergies and allergic to many different animals, all from an unknown date and unknown if ongoing. Concomitant medication included sertraline hydrochloride (ZOLOFT) and gabapentin. The patient previously took KEFLEX and experienced allergies. On 06Jan2021 12:00 PM, the patient experienced left arms swollen lymph nodes, runny nose, sore throat, headache and fatigue. Treatment received included Zpak. The patient was not pregnant at the time of vaccination. The most recent COVID-19 vaccine was administered in a nursing home/senior living facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Adverse events resulted in doctor or other healthcare professional office/clinic visit. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. The patient underwent lab tests and procedures which included Covid nasal swab: negative and rapid Covid test: negative, both on 07Jan2021. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds: ZOLOFT;

Current Illness:

ID: 0954519
Sex: M
Age:
State: CT

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fever of 103.8; Chills; Body aches; This is a spontaneous report from a contactable other healthcare professional (reported for himself). A 32-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date were unknown), second dose on 11Jan2021 at 10:00 and first dose on 22Dec2020 at 15:00; both via an unspecified route of administration on his left arm at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient had no allergies to medications, food and other products. Prior to vaccination, the patient was not diagnosed with COVID-19. No vaccines received within 4 weeks prior to COVID vaccine. On 12Jan2021 at 2:00, the patient experienced fever of 103.8 (unit not reported), chills and body aches. The patient did not receive treatment for the adverse events. The patient has not recovered from the events. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0954520
Sex: F
Age:
State: CA

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

Lab Data: Test Name: Covid; Test Result: Positive ; Comments: a week after taking the 1st dose of vaccine

Allergies:

Symptoms: caller tested positive on covid a week after taking the 1st dose of vaccine; caller tested positive on covid a week after taking the 1st dose of vaccine; This is a spontaneous report from a contactable consumer (patient) via Pfizer-sponsored program Pfizer First Connect. A female patient of an unspecified age received the 1st dose of bnt162b2 (BNT162B2) at single dose on an unspecified date for Covid-19 immunisation. The patient medical history was and concomitant medications were not reported. The patient was tested positive for Covid a week after taking the 1st dose of vaccine on an unspecified date. The outcome of events was unknown. Patient wanted to know if she can get the second dose. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0954521
Sex: F
Age:
State: GA

Vax Date: 01/06/2021
Onset Date: 01/01/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: Temperature; Result Unstructured Data: Test Result:99-100 Fahrenheit

Allergies:

Symptoms: headache; feeling achey/extreme body aches; Chills; Temperature 99-100F; This is a spontaneous report from a contactable nurse (patient). A 25-year-old female patient received the 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EJ1685 and expiry date: unknown), intramuscular on the left arm on 06Jan2021 07:30 at a single dose for COVID-19 immunisation. Medical history included Spinal fusion L4-S1, latex and adhesive allergy. Concomitant medication included sertraline hydrochloride (ZOLOFT). The patient previously took BACLOFEN and BACRIM and experienced allergy, and the first dose of BNT162B2 for covid 19 immunization on an unspecified date. The patient started feeling achey 10-12 hours after second dose on 06Jan2021 17:30. By 2300 that night, there were extreme body aches and headache. Patient was still achey throughout following day on 07Jan2021. She was feeling better, but on 11Jan2021 started feeling achey again. She had chills and temperature was 99-100F on Jan2021. Outcome of the events was unknown. No treatment was received for the events. Patient was not diagnosed with COVID-19 prior to vaccination and had not been tested since the vaccination.

Other Meds: ZOLOFT

Current Illness:

ID: 0954522
Sex: M
Age:
State: AL

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: body temperature; Result Unstructured Data: Test Result:100 Fahrenheit; Comments: 100 degree fever

Allergies:

Symptoms: feeling bad; 100 degree fever; chills; body aches; headache; This is a spontaneous report from a contactable nurse. A 45-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number CH9899), via an unspecified route of administration from 11Jan2021 08:30 to 11Jan2021 08:30 at a single dose for covid-19 immunization. The patient's medical history was not reported. Historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) On 21Dec2020 at first dose. Concomitant medication included melatonin. It was reported that the patient feeling bad after injection, got 100 degree fever, chills, body aches and headache; all on 11Jan2021 16:00. Took aspirin to reduce side effects but headache remains. The outcome of the event headache was not recovered while recovering for the other events.

Other Meds:

Current Illness:

ID: 0954523
Sex: F
Age:
State: MT

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

Lab Data:

Allergies:

Symptoms: Severely sick after second dose; This is a spontaneous report from a non-contactable consumer. An adult female patient received the 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date: not reported), via an unspecified route of administration in Jan2021 at single dose for Covid-19 immunization. The patient received the first dose of BNT162B2 on an unspecified date. The patient's medical history and concomitant medications were not reported. The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. It was reported that the patient was severely sick after second dose "never been so sick" in Jan2021. It was unknown if there was a treatment received for the adverse event. It was unknown if the patient has been tested for COVID-19 since the vaccination. The outcome of event was unknown. This case is non-serious. No follow-up attempts are possible, information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0954524
Sex: F
Age:
State: KS

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: fever; Result Unstructured Data: Test Result:99.8; Comments: at 20:00

Allergies:

Symptoms: Dose1 start time 28Dec2020, dose 2 start time 11Jan2021; Red, inflamed, hot to touch injection site; Red, inflamed, hot to touch injection site; Red, inflamed, hot to touch injection site; Chills; fever- 99.8; severe headache (migraine); This is a spontaneous report from a contactable nurse (patient) reported for herself. A 56-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; brand=Pfizer, lot number=Ek9231) intramuscularly at left arm on 11Jan2021 at 01:30 PM at a single dose (dose number:2) for COVID-19 immunization. Medical history included type 2 diabetes mellitus (DM) and known allergies to latex. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Other medications the patient received within 2 weeks of vaccination included metformin, atorvastatin, lisinopril, exenatide (BYDUREON) and bimatoprost (LUMIGAN). Historical vaccination included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; brand=Pfizer, lot number= Ek5730) intramuscularly at left arm on 28Dec2020 at 02:30 PM at a single dose (dose number:1) for COVID-19 immunization. The patient was not pregnant at the time of vaccination. Facility where the most recent COVID-19 vaccine was administered was at hospital. The patient experienced adverse events included "red, inflamed, hot to touch injection site", chills, fever- 99.8, and severe headache (migraine); all with start dates on 11Jan2021 at 08:00 PM. The events were reported as non-serious. No treatment received for events. The outcome of events was resolving. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19.

Other Meds: ; ; ; BYDUREON; LUMIGAN

Current Illness:

ID: 0954525
Sex: F
Age:
State: TX

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: Test Name: BP; Result Unstructured Data: Test Result:unknown results; Test Name: CXR; Result Unstructured Data: Test Result:unknown results; Test Name: EKG; Result Unstructured Data: Test Result:unknown results; Test Name: HR; Result Unstructured Data: Test Result:161; Test Name: HR; Result Unstructured Data: Test Result:110-115; Test Name: HR; Result Unstructured Data: Test Result:normal; Test Name: HR; Result Unstructured Data: Test Result:115-125; Test Name: Labwork; Result Unstructured Data: Test Result:unknown results

Allergies:

Symptoms: 3.5 hours after injection all of a sudden HR was at 161; Muscle pain around injection site and some fatigue, but not bad.; Muscle pain around injection site; Muscle pain around injection site and some fatigue, but not bad.; I was warmflush feeling; When HR jumped to 161 she had a weird sensation run down both of arms; This is a spontaneous report from a contactable consumer. This 40-year-old female (no pregnant) patient received first dose of BNT162B2 (lot# EL3249) on 08Jan2021 02:30 PM on arm Left for COVID-19 immunization. Medical history was Type 1 IDDM (Diabetes), Anxiety/Panic Disorder. Concomitant drug included desvenlafaxine succinate (PRISTIQ), Clonazepam, insulin lispro (HUMALOG), cetirizine hydrochloride (ZYRTEC), all received within 2 weeks of vaccination. Past drug was Allergies to levofloxacin (LEVAQUIN). It was reported that 3.5 hours after injection (08Jan2021 06:00 PM) all of a sudden HR was at 161, patient layed down and it came down a little to 115-125, for 4-5 thereafter it stayed around 110-115, and after about 6 hours it returned to normal. She was warm flush feeling but without a fever. When HR jumped to 161 she had a weird sensation run down both of arms but is subsided with kaying down and HR coming down a bit. No toher bad issues since. Muscle pain around injection site and some fatigue, but not bad. Emergency room/department or urgent care visit. Treatment: EKG, CXR, Labwork, very brief monitoring of HR/BP. Outcome of the event was recovered. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient had not been tested for COVID-19. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No follow-up attempts are needed. No further information is expected.

Other Meds: PRISTIQ; ; HUMALOG; ZYRTEC [CETIRIZINE HYDROCHLORIDE]

Current Illness:

ID: 0954526
Sex: F
Age: 35
State: CA

Vax Date: 01/16/2021
Onset Date: 01/16/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: None

Allergies: N/A

Symptoms: Fatigue, sore arm with red swollen nodule at site. Nausea, vomiting, body-aches, and headache lasting almost 3 days.

Other Meds: N/A

Current Illness: N/A

ID: 0954527
Sex: F
Age:
State: NJ

Vax Date: 01/08/2021
Onset Date: 01/09/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data:

Allergies:

Symptoms: mild redness; mild swelling; itchy; burning; swelling to the eye; mild rash around her left eye; This is a spontaneous report from a contactable nurse reported for herself. This 42-year-old female patient (No pregnant) received the second dose of the BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on an 08Jan2021, 10:45 AM on Right arm at single dose for covid-19 immunisation. Medical history included juvaderm under her eye approximately 1 year and half to two years ago. Prior to vaccination, the patient did not diagnose with COVID-19. No Allergies to medications, food, or other products. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously received the first dose of the BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at age of 42-year-old on an 18Dec2020, 11:15 AM on Right arm at single dose for covid-19 immunisation. Day after the 2nd dose, the patient had a mild rash around her left eye only on 09Jan2021. 3rd day (11Jan2021) swelling to the eye. The day of this report is 4 days post vaccine (12Jan2021), the patient mild redness mild swelling but remain itchy and burning. The patient did not report to her dr as the symptoms seem to be resolving on its own. No covid tested post vaccination. No treatments were received. Outcome of the events was recovering. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0954528
Sex: F
Age: 23
State:

Vax Date: 01/15/2021
Onset Date: 01/16/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data:

Allergies: None

Symptoms: Did not start developing symptoms until the night of with body aches and hot flashes. Then the next day body aches from the waist down, was unable to stand for more than 2 mins. Sitting down had mild relief. Then fatigue, fever, cough, headache, chills/hot flashes. Symptoms started to fade down towards the end of the day. Just still feverish, headache, and cough. Treatment tried are two 500 MG of tylenol, sleep, and Vicks rub. The next day, only had a headache and cough which had resolved overnight.

Other Meds:

Current Illness: None

ID: 0954529
Sex: F
Age:
State: NJ

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

Lab Data:

Allergies:

Symptoms: severe chills; severe nausea (no vomiting); headache; neck aches; This is a spontaneous report from a contactable physician (reported for herself). A 41-year-old female patient (Pregnant at the time of vaccination) received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: el3248), via an unspecified route of administration on 10Jan2021 08:30 at single dose for COVID-19 immunization. The patient's medical history included Allergies to amoxicillin. The patient's concomitant medications were not reported. The patient previously took the first dose of bnt162b2 (lot number: ek9231) on 22Dec2020 21:45 at single dose for COVID-19 immunization. Facility where the most recent COVID-19 vaccine was administered at Hospital. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced severe chills, severe nausea (no vomiting), neck aches, headache on 10Jan2021 20:30. Treatment received for the adverse events included tylenol 1g x3 doses. The events were non-serious per the reporter. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hadn't been tested for COVID-19. The outcome of the events was recovered in Jan2021.

Other Meds:

Current Illness:

ID: 0954530
Sex: F
Age:
State: NM

Vax Date: 12/16/2020
Onset Date: 01/01/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data:

Allergies:

Symptoms: left subscapular lymphnode swelling with tenderness; left subscapular lymphnode swelling with tenderness; This is a spontaneous report from a contactable nurse. A 45-year-old female patient started to receive bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EH9899), via an unspecified route of administration from 16Dec2020 11:15 to 16Dec2020 11:15 at a single dose for covid-19 immunization. Medical history included seasonal allergy and Sulfa drugs Allergies. Concomitant medication included minerals nos, vitamins nos (CENTRUM A to Z) and naproxen sodium (ALEVE). The patient had left subscapular lymph node swelling with tenderness on 01Jan2021. The outcome of the events was recovering.

Other Meds: CENTRUM A TO ZINC; ALEVE

Current Illness:

ID: 0954531
Sex: F
Age: 33
State: UT

Vax Date: 01/16/2021
Onset Date: 01/16/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: no

Allergies: No

Symptoms: After the first dose at noon 1/16/2021 mountain time, I began to have a fever in the evening, starting from 101 F, then it went up to 104 F at midnight, feel chill and body aches, bad headache. I never had such high temperature in my lifetime. I took ibuprofen and it seems the fever went away in the next early morning 1/17. However, my temperature went up again 101.3 F at noon 1/17 and it went up to 103 F at night 1/17. I consulted the doctor and took Tylenol. 1/18 the fever was way but still headache, body aches and feel very weak.

Other Meds: regular taken levothyroxine for Hashimoto but not taken on the day of vaccine

Current Illness: Hashimoto

ID: 0954532
Sex: F
Age:
State: MD

Vax Date: 12/30/2020
Onset Date: 12/31/2020
Rec V Date: 01/19/2021
Hospital:

Lab Data:

Allergies:

Symptoms: I am very off balance; Dizziness; It's gotten worst to the point I can hardly get out of bed in the morning; I am having vertigo. It was mild at first but now it's gotten worst to the point I can hardly get out of bed in the morning; This is a spontaneous report from a contactable nurse (patient) A 59-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EL1284), via an unspecified route of administration on 30Dec2020 at single dose for COVID-19 immunisation. Medical history was none. There were no concomitant medications. The patient experienced vertigo on 31Dec2020. The patient reported that it was mild at first but now it's gotten worst to the point she can hardly get out of bed in the morning on unknown date. After sleep of about 2 hours it was better but she had been up for over all 2 hour that morning and it was still, the patient was very off balance on unknown date. The patient experience also dizziness on an unspecified date. The outcome of vertigo was not recovered, for the other events was unknown. No treatment as performed for the event vertigo.

Other Meds:

Current Illness:

ID: 0954533
Sex: F
Age:
State: FL

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: Test Name: temperature; Result Unstructured Data: Test Result:97.2 (+), or (-), 98.6; Comments: normal temperature

Allergies:

Symptoms: Pain at injection site; swelling,(size of my palm,); warm to touch, all over body; muscle aches, especially shoulder blades; tired/sleepy; tired/sleepy; chills; This is a spontaneous report from a contactable other HCP (patient). This 64-year-old female other HCP reported that she received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number=EL128H), via unspecified route at right arm on 08Jan2021 07:45 AM at single dose for COVID-19 immunization. Facility type vaccine was hospital. Medical history included elevated blood pressure and atrial septal defect repair 2008. Concomitant medications included olmesartan medoxomil and hydrochlorothiazide. Historical vaccine included the first dose of BNT162B2 (lot# EH9899) on 18Dec2020 at age of 64 years old for COVID-19 immunization and having arm pain. No Covid prior vaccination. No Covid tested post vaccination. No known allergies. On 08Jan2021 07:00 PM, patient experienced pain at injection site, swelling (size of her palm), warm to touch all over body and muscle aches, especially shoulder blades, very tired/sleepy with chills. No treatment was received. It was reported normal temperature for patient was 97.2 (+) or (-) 98.6. Outcome of events was recovering.

Other Meds: OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE

Current Illness:

ID: 0954534
Sex: F
Age: 29
State: CA

Vax Date: 01/11/2021
Onset Date: 01/18/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data:

Allergies: Alcohol

Symptoms: Pfizer-BioNTech COVID-19 Vaccine EUA Diarrhea Tiredness Slight Chills

Other Meds:

Current Illness:

ID: 0954535
Sex: F
Age:
State:

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data:

Allergies:

Symptoms: pain at injection site; body aches; headache; This is a spontaneous report from a contactable consumer (patient's husband). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), via an unspecified route of administration on 06Jan2021 at single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. On 06Jan2021, the patient experienced pain at injection site, body aches and headache. Clinical outcome of the events was unknown. Information about lot and batch number was requested.

Other Meds:

Current Illness:

ID: 0954536
Sex: M
Age:
State: WA

Vax Date: 12/22/2020
Onset Date:
Rec V Date: 01/19/2021
Hospital:

Lab Data: Test Name: COVID-19 virus test; Test Result: Positive

Allergies:

Symptoms: COVID-19 virus test positive; COVID-19 virus test positive; This is a spontaneous report from a Pfizer-sponsored program "Pfizer First Connect" from a contactable consumer reporting for himself. A male patient of an unspecified age received the 1st dose of bnt162b2 (BNT162B2), via an unspecified route of administration, on 22Dec2020, at single dose, for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced COVID-19 virus test positive on an unspecified date with outcome of unknown. It was reported that the patient was scheduled to get his second dose on 12Jan2021, however between 22Dec2020 and 12Jan2021 the patient experienced the adverse event. The information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0954537
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: some pain at the injection site; This is a spontaneous report from a contactable other healthcare professional via Pfizer sales representative. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not reported), 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 patient experienced some pain at the injection site after use of product. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 0954538
Sex: F
Age: 58
State: AZ

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

Lab Data: No w

Allergies: Penicillins , Morpheme, gluten, dilaudid, darvocet

Symptoms: Nauseous, extremely sore and aching muscles and body, migraine

Other Meds: Vitamin d, vitamin c, CBD, theanine, herbal tincture for anxiety and stress

Current Illness: Immune system down

ID: 0954539
Sex: F
Age:
State:

Vax Date: 01/08/2021
Onset Date: 01/01/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data:

Allergies:

Symptoms: 24 hoursMalaise; flu like symptoms; This is a spontaneous report from a non-contactable Physician reporting for herself. The case was also reported via Pfizer employee. A 32-year-old female patient (non-pregnant) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 08Jan2021 at single dose in the right arm for COVID-19 immunisation. The patient was vaccinated at hospital. No other vaccine was given within 4 weeks prior to the COVID vaccine. Historical vaccine included first dose of BNT162B2 administered on an unspecified date. The patient's medical history was not reported. The patient had no allergies to medications, food, or other products. The patient did not receive concomitant medications. On 08Jan2021 the patient experienced 24 hours malaise and in Jan2021 flu like symptoms. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, she has not been tested for COVID-19. The patient received treatment with paracetamol (TYLENOL) for the event malaise. Malaise resolved on 09Jan2021, while outcome of flu like symptoms was unknown. No follow-up attempts are possible; information about batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 0954540
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Got the first dose and was contracted with COVID; Got the first dose and was contracted with COVID; This is a spontaneous report from a contactable consumer (patient) from a Pfizer-sponsored program IBCC (Inbound Call Center for HCPs). 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 20Dec2020 at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient was contracted with covid on an unspecified date in Dec2020 (27Dec2020 or 28Dec2020) with outcome of unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0954541
Sex: F
Age:
State: CO

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

Lab Data:

Allergies:

Symptoms: throat swelling; headache; Pain; little bit of chills; GI upset; This is a spontaneous report from a contactable nurse. A 48-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot: EK9231, expiry: 30Apr2021), via an unspecified route of administration on an unspecified date at 0.3 mL, single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received her first dose of bnt162b2 on an unknown date for covid-19 immunization and experienced pain at the injection site. On an unspecified date, the patient experienced head ache, throat swelling, gastrointestinal (GI) upset, pain, and little bit of chills (don't believe to have had fever). It was clarified that the event took place after use of product. The outcome of the events was unknown.; Sender's Comments: The information in this report is limited, and does not allow a full medically meaningful assessment of the case. Considering temporal relationship, a causal relationship between the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) and the reported events including throat swelling cannot be excluded. 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.

Other Meds:

Current Illness:

ID: 0954542
Sex: U
Age:
State:

Vax Date: 01/07/2021
Onset Date: 01/07/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Burning and itchy eyes; Burning and itchy eyes; This is a spontaneous report from a non-contactable consumer (the patient). A patient of unspecified age and gender received bnt162b2 (BNT162B2) vaccine, via an unspecified route of administration on 07Jan2021 10:45 at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient stated that starting 07Jan2021 at 17:00 it started burning and itchy eyes. 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: 0954543
Sex: F
Age:
State: NY

Vax Date: 01/05/2021
Onset Date: 01/06/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Injection site swelling and redness; Injection site swelling and redness; Low grade fever; Nausea; This is a spontaneous report from a contactable nurse reporting for herself. A 54-year-old female patient received bnt162b2 (BNT162B2) (Lot# EJ1686, Exp date 31Mar2021), via an unspecified route of administration, on 05Jan2021, at single dose, for COVID-19 immunisation. Medical history and concomitant medications were none. The patient experienced injection site swelling and redness, low grade fever and nausea all on 06Jan2021 with outcome of unknown. Therapeutic measures were taken as result of the events and included treatment with a 1000 mg Tylenol. The events were considered related (source of assessment: primary source reporter, method of assessment: global introspection).

Other Meds:

Current Illness:

ID: 0954544
Sex: M
Age:
State: NY

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: Test Name: Fever; Result Unstructured Data: Test Result:102.4; Test Date: 202012; Test Name: Physical; Result Unstructured Data: Test Result:Unknown results

Allergies:

Symptoms: This morning it started all these different side effects and it's progressively getting worse, so I left work; Body aches; Headache; Stomach issues; pain; Diarrhea; Chills; Fever I just checked it's 102.4; Little sore arm at night; This is a spontaneous report from a contactable consumer (patient). A 56-year-old male patient received the 1st dose of bnt162b2 (BNT162B2, Batch/lot # EK9231) at single dose on 06Jan2021 around 2 O'clock for Covid-19 immunisation, administered ad hospital. Medical history included high cholesterol, hypertension, irregular heart beats, arrhythmia, acid reflux. Concomitant medication included amlodipine (AMLODIPINE) 10 mg once a day for hypertension, acetylsalicylic acid (BABY ASPIRIN) at 81 mg, once a day, carvedilol (CARVEDILOL) at 12.5 mg, two times a day hypertension, flecainide (FLECAINIDE) at 50 mg, twice a day for irregular heart beats, arrhythmia, olmesartan (OLMESARTAN) at 40 mg once a day for hypertension, omeprazole (OMEPRAZOLE) at 40 mg when needed for acid reflux, rosuvastatin (ROSUVASTATIN) at 20 mg, once a day for high cholesterol. The patient experienced little sore arm at night on 06Jan2021. Then, on 07Jan2021 morning he went in to work and it started all these different side effects and it's progressively getting worse, so he left work at abut 10 O' clock AM. He was getting body aches, headache, stomach issues, pain, diarrhea, chills, and fever I just checked it's 102.4 on 07Jan2021. The patient underwent lab tests physical examination with unknown results in Dec2020 3 weeks before this report (he had complete physical lab work with his doctor). Treatment included taking Tylenol and Advil. The outcome of all events was not recovered. Due date of second shot will be 23Jan2021.

Other Meds: ; BABY ASPIRIN; ; ; ; ;

Current Illness:

ID: 0954545
Sex: F
Age:
State: VT

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

Lab Data:

Allergies:

Symptoms: Muscle ache; Joint pain; Arm still hurt/arm was really sore and my neck was sore/ forearms blades; Arm still hurt/arm was really sore and my neck was sore; Her shoulder, knee blades; Her shoulder, knee blades; This is a spontaneous report from a contactable nurse reporting for herself. A 60-year-old female patient received bnt162b2 (BNT162B2) (lot# EL1284), via an unspecified route of administration, in Jan2021, at single dose, for COVID-19 immunisation. Medical history and concomitant medications were none. The patient experienced muscle ache, joint pain, arm still hurt/arm was really sore and my neck was sore/ forearms blades; her shoulder, knee blades all in Jan2021 with outcome of unknown. Therapeutic measures were taken as a result of the events and included treatment with ibuprofen and Tylenol.

Other Meds:

Current Illness:

ID: 0954546
Sex: M
Age:
State: NM

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

Lab Data:

Allergies:

Symptoms: Itchy Palm Rash broke out and spread to wrist and arm; This is a spontaneous report from a contactable physician (patient). This report was received via a sales representative. A male patient of an unspecified age received bnt162b2 (COVID 19 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. The patient experienced itchy palm rash broke out and spread to wrist and arm on an unspecified date. The adverse event took place after Pfizer product use. Outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0954547
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: malaise; myalgias; This is a spontaneous report from a contactable physician (patient's parent). A 27-year-old male patient received second dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine; lot/batch number and expiry date were unknown), 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 patiently previously received first dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine) at a single dose for COVID-19 immunization. The patient experienced malaise and myalgias which took place after the administration of second dose. He took Tylenol 6 hours ago, and the symptoms are decreasing. The outcome of the events was recovering. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0954548
Sex: F
Age: 27
State: PA

Vax Date: 01/15/2021
Onset Date: 01/16/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: None at this point

Allergies: None

Symptoms: Large red circle around injection site, hot, itchy, painful that continues to expand even at day 4

Other Meds: Womans multivitamin, tri sprintec

Current Illness: None

ID: 0954549
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: headache; fatigue; pain at the injection site; This is a spontaneous report from a non-contactable consumer. A male patient of unspecified age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiration date: unknown), 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 the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) for COVID-19 immunization on an unspecified date. The reporter mentioned that the patient received the COVID-19 vaccine series. The patient experienced headache and fatigue after the second injection (same day) and pain at the injection site, all on unspecified date. The outcome of the events was unknown. No follow-up attempts are possible; information on the lot/batch number could not be obtained.

Other Meds:

Current Illness:

ID: 0954550
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: arm pain; chills; This is a spontaneous report received from a non-contactable consumer (patient's sister). A female patient of an unspecified age received the second dose of BNT162B2 (BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), 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 patient received the vaccine and after the second dose experienced arm pain and chills that same day (unspecified date). The outcome of the events was unknown. No follow up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0954551
Sex: M
Age:
State: NJ

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

Lab Data:

Allergies:

Symptoms: feeling weak; tired; This is a spontaneous report received from a contactable physician (also reported as consumer). A male patient of an unspecified age (reported as "over the age of 60") received the second 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 single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced feeling weak and tired a few hours after receiving his second vaccination (unspecified date). The outcome of the events was unknown. No follow-up attempts are possible. Information about batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 0954552
Sex: F
Age: 34
State: CA

Vax Date: 01/17/2021
Onset Date: 01/18/2021
Rec V Date: 01/19/2021
Hospital:

Lab Data: n/a

Allergies: none

Symptoms: Numbness in L hand developing 3 hours after the second dose, which occurred while I was asleep and then woke up and then went away within 5 minutes. Today, 1/18/2020, I developed dark red blotches on my L hand, especially visible near the knuckles (the metacarpophalangeal joints). It then went away within 3 minutes but then appeared on other parts of my hand, including on my R hand. The blotches all went away within 2-3 minutes but occurred consecutively in different parts of my hand (i.e., some area developed the blotchiness prior to others, and then other parts developed it)

Other Meds: aripiprazole lamotrigine

Current Illness: none

ID: 0954553
Sex: F
Age:
State: CA

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

Lab Data:

Allergies:

Symptoms: vomiting; Headache; This is a spontaneous report from a contactable consumer from a Pfizer sponsored program Pfizer First Connect. A female patient of an unspecified age received 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 experienced headaches and vomiting on an unspecified date. Outcome of event was unknown. Information on the Lot/Batch number has been requested

Other Meds:

Current Illness:

ID: 0954554
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: malaise; cough; This is a spontaneous report received from a contactable other healthcare professional. 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 single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Four days after the patient's COVID-19 vaccine (unspecified date), the patient started experiencing malaise and cough. 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:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm