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**
PLEASE CHECK BACK SOON
Download the files above while you wait.







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: 1000105
Sex: F
Age:
State: WA

Vax Date: 01/15/2021
Onset Date: 01/19/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: feeling nauseous; vomiting; indigestion; belching; This is a spontaneous report from a Pfizer-sponsored Program, from a contactable consumer. A 63-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1686, expiry date: Mar2021), intramuscular on 15Jan2021 on left arm at a single dose for COVID-19 immunisation. The patient had no medical history. There were no concomitant medications. The patient got her first shot for the vaccine last Friday afternoon (15Jan2021). Yesterday early evening (19Jan2021), she was feeling nauseous and was vomiting. She wanted to know if it was an adverse effect from the COVID-19 vaccine even though it was the 4th day after getting the COVID-19 vaccine. She also mentioned that she ate a bunch of pistachios and wasn't sure if that was a contributing factor to what she was experiencing. The patient experienced indigestion, belching, and vomiting on 19Jan2021. She is feeling okay now and asked if that was normal. She confirmed contact details. She was asking if it was normal to have the side effects 4 days after getting the vaccine. She is so much better and has not vomited since 07:30 this morning. She has improved within the last hour. She still has tightness in her upper intestines, but it could be because she is hungry since she has not had anything since yesterday. She is glad she is feeling better. Stated the indigestion could be from all the pistachios that she ate at work. She took tums. She still had indigestion and ate a small dinner. She kept vomiting after, and it was more of a liquid. She put her glasses on. She has a hard time seeing the lot number on the card she was provided, stating it is so small Dose reported as 30mcg or 0.3ml. The outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 1000106
Sex: M
Age:
State: AK

Vax Date: 12/18/2020
Onset Date: 12/18/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Name: Blood work; Result Unstructured Data: Test Result:Unknown Results; Test Date: 20201218; Test Name: Temperature; Result Unstructured Data: Test Result:97.7 to 99.9; Comments: for 5-6 days were at 99.9 never breaking 100; Test Date: 20210111; Test Name: Temperature; Result Unstructured Data: Test Result:97.7 to 99.9; Comments: for 5-6 days were at 99.9 never breaking 100

Allergies:

Symptoms: scheduled for the same day as the 2nd Hep B vaccine; scheduled for the same day as the 2nd Hep B vaccine/ realized they were not supposed to give vaccinations like that, the error was caught; Received his first dose of Covid19 vaccine on 18Dec2020/ Received his second Covid vaccine on 11Jan2021; Pain in the left arm; Felt woozy/Small bouts of dizziness; Felt nausea; Not too much pain around the injection site; Rise in temperature of 97.7 to 99.9; This is a spontaneous report from a contactable consumer reporting for himself. A 32-years-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 18Dec2020 08:45 at single dose, left arm (lot number EK5730); and second dose via an unspecified route of administration on 11Jan2021 at single dose, right arm (lot number EJ1685) for COVID 19 prevention; hepatitis b vaccine (manufacturer unknown), via an unspecified route of administration on 14Dec2020 at single dose (arm once) for immunisation (Prerequisites of working in long term care facility). Medical history reported as none. There were no concomitant medications. The patient received the Pfizer-Biontech Covid19 vaccine in within a close interval with a Hepatitis B vaccination. On 14Dec2020, patient received the Hepatitis B vaccination 4 days prior to COVID-19 vaccine which patient reported was not recommended, then received his first dose of Covid19 vaccine on 18Dec2020 (he was 32 years old at that time, he turned 33 years old on 25Dec2020). He received his second COVID vaccine on 11Jan2021. Patient reported he has since learned that a dosing interval of 14 days is usually recommended. Patient stated this was not supposed to be done within 14 days. He stated that CDC mentioned that three vaccines that were possible to do this but unknown safety hazards to doing this. Stated that it did not mention Hepatitis B. Stated it was an error on nurse's judgement. He stated there was a second co-administration to happen on Monday, patient was scheduled for the same day as the 2nd Hep B vaccine (unknown date), but that she was on vacation. He stated that the person could not find Hepatitis B vaccine. He stated that his original paperwork was not filed. He stated that he got a second COVID 19 on Monday, and on Wednesday (13Jan2021) they realized they were not supposed to give vaccinations like that, the error was caught, and he would not get the second Hepatitis B vaccine. Stated that he was unaware of any symptoms that occurred immediately after vaccination. He wanted to know how to proceed from this point. Patient stated that It was the person in charge of vaccinations told him there was no problem giving co-administration of COVID-19 vaccine. He also reported mild adverse events after both COVID vaccines which include not too much pain around the injection site, some nausea 10-12 hours after the injection; felt woozy/small bouts of dizziness, pain in the left arm at 17:00 (to point could not lift or sleep on it), rise in temperature of 97.7 to 99.9 (also reported as for 5-6 days were at 99.9 never breaking 100) on 18Dec2020. Treatment was not given for all events. Patient had blood work done on an unspecified date with unknown results, and rise in temperature of 97.7 to 99.9 on 18Dec2020 and 11Jan2021. Outcome of the events rise in temperature of 97.7 to 99.9, pain in the left arm was recovered on an unspecified date; events felt woozy/small bouts of dizziness and felt nausea was recovered on 18Dec2020, while outcome of not too much pain around the injection site was unknown.

Other Meds:

Current Illness:

ID: 1000107
Sex: F
Age:
State: MI

Vax Date: 01/15/2021
Onset Date: 01/18/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Name: Heart rate; Result Unstructured Data: Test Result:normally 70 or 72; Test Date: 20210118; Test Name: Heart rate; Result Unstructured Data: Test Result:93 (elevated)

Allergies:

Symptoms: Heartbeat was elevated to 93, where it is normally 70 or 72/heartbeat intermittently going faster when going up the stairs; This is a spontaneous report from a contactable consumer (patient). A 73-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL3249; Expiration date was not reported) on 15Jan2021 at a single dose on the left arm, with route of administration unspecified, for COVID-19 immunization. The patient had no relevant medical history and concomitant medications. On 18Jan2021, the patient's heartbeat was elevated at 93 where it was normally 70 or 72. The patient' fast heartbeat was intermittently going faster when going up the stairs, and it was unusual for her. The outcome of the event, elevated heartbeat, was unknown.

Other Meds:

Current Illness:

ID: 1000108
Sex: M
Age:
State:

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210120; Test Name: Blood Pressure; Result Unstructured Data: Test Result:Fine; Test Date: 20210120; Test Name: Temperature; Result Unstructured Data: Test Result:High; Test Date: 20210120; Test Name: Heart Rate; Result Unstructured Data: Test Result:92

Allergies:

Symptoms: felt like his throat was closing up; dizziness; trouble with his vision/couldn't see right; numbness in the face; the feeling of this AE as being "intoxicated"; 15 minutes after, he started to not feel well/not feeling good at all; was not able to drive; high temperature; having chills; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: not provided), via an unspecified route of administration on 20Jan2021 10:30 AM at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient got the Pfizer COVID-19 vaccine today (20Jan2021) at 10:30AM. Within the 15-20 minutes after getting the shot, he felt fine. About 15 minutes after, patient started to not feel well. He said he was not able to drive, he had a high temperature, he was having chills, and not feeling good at all. Patient mentioned that he also had trouble with his vision. Patient also experienced numbness in the face and dizziness. He had an ambulance check him and they told him that his blood pressure was fine and his heart rate was at 92. Patient added that he felt like his throat was closing up. He described the feeling of this AE as being "intoxicated". Patient also emphasized that he "couldn't see right". Outcome of the events was unknown. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1000109
Sex: F
Age:
State: NM

Vax Date: 12/23/2020
Onset Date: 12/23/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: feeling unwell; dizzy; dry heaving; This is a spontaneous report received from a contactable pharmacist. A 52-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1284, expiry date: unknown), intramuscular in the left arm, on 23Dec2020 17:30, at single dose, for COVID-19 immunization, in the hospital. Medical history included allergies to contrast dye, obesity, osteoarthritis (OA), hyperlipidemia and being pre-diabetes. The patient was not pregnant during the time of vaccination. Concomitant medication included atorvastatin, meloxicam and multivitamins. The patient did not receive any other vaccines within four weeks prior to BNT162B2. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not tested for COVID-19 since the vaccination. The patient experienced feeling unwell, dizzy and was dry heaving on 23Dec2020 17:30. No treatment was given for the events. The reporter assessed the events as non-serious. The outcome of the event was recovered on an unspecified date.

Other Meds: ATORVASTATIN; MELOXICAM; MULTIVITAMIN [VITAMINS NOS]

Current Illness:

ID: 1000110
Sex: F
Age:
State: MO

Vax Date: 01/15/2021
Onset Date: 01/19/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210119; Test Name: fever; Result Unstructured Data: Test Result:100.2

Allergies:

Symptoms: headache; fever of 100.2; fatigue; This is a spontaneous report from a contactable other healthcare professional (patient herself). A 36-year-old female patient (not pregnant) received her first dose of bnt162b2 (BNT162B2 also reported as COVID 19, brand Pfizer-Biontech, lot EL1284), via an unspecified route of administration in left arm 15Jan2021 13:00 at SINGLE DOSE for Covid-19 immunisation. Medical history included joint hyper mobility and allergy to grapefruit and beestings. No Covid prior vaccination. No other vaccine in four weeks. Other medications in two weeks was daily multivitamin (unspecified). On 19Jan2021 (4 days following injection), she developed headache, fever of 100.2 and fatigue. No treatment was given. The outcome of events was recovering. No Covid tested post vaccination.

Other Meds:

Current Illness:

ID: 1000111
Sex: F
Age:
State: AZ

Vax Date: 01/18/2021
Onset Date: 01/19/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: rash on chest/It is just itching/she noticed it was a little worse. It is more red; rash on chest/It is just itching/she noticed it was a little worse. It is more red; This is a spontaneous report from a contactable consumer (patient). A 64-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: not provided), via an unspecified route of administration on 18Jan2021 at single dose for COVID-19 immunization, reported as "prevent COVID 19". Medical history included ongoing allergy to penicillin. There were no concomitant medications and investigation assessment. On 19Jan2021, the patient developed rash on chest. She wanted to know if she can put something topical in it or if she could take antihistamines to treat the rash. 20Jan2021 (today), it was not hurting but reported that it was just itching. Patient was wondering if she can put a topical on it. Patient has had no trouble breathing. She gets the same rash when she was in the sun too much. Patient signed up for V-safe. The patient does not have her doctor information. She just got a new doctor. Patient reported that it got better last night, but then this morning she noticed it was a little worse. It was more red. She drove with her husband when he got his, and they offered her a vaccine too. She got it to not get COVID 19. Outcome of the event was not recovered (reported as ongoing). Information on the lot/ batch number has been requested.

Other Meds:

Current Illness: Penicillin allergy

ID: 1000112
Sex: F
Age:
State: CT

Vax Date: 01/03/2021
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: diarrhea; go back and forth throwing up; feel nauseas almost every day; injection site started hurting; Headache; when she's breathing she feel like her lungs are cold; she cannot breathe good; feels like they (lungs) were burning; felt like she had the flu; felt like she was hit by truck; she has not been feeling well/not felt very good/felt really sick; This is a spontaneous report from a contactable consumer (patient) reported that a 38-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1284), via an unspecified route of administration on the left arm on 03Jan2021 14:00 at a single dose as precaution for working in the healthcare field. The vaccine was administered at the Long-Term Care for facility. Medical history included had trouble breathing due to asthma that was diagnosed at age of 16. Concomitant medications included amitriptyline taken from an unspecified date for 6 years for interstitial Cystitis and it helps her sleep at night. After she got it (vaccine), her injection site started hurting and headache on 03Jan2021 that there went away a couple of hours after getting vaccination. Sometimes when she's breathing she feel like her lungs are cold, she cannot breathe good, and feels like they (lungs) were burning on 03Jan2021. Also, it was reported that ever since she got a first dose of the vaccine she has not been feeling well/not felt very good on Jan2021. She goes back and forth throwing up on 05Jan2021, and feel nauseas almost every day on 04Jan2021. When she got it, for the last of these 2 days (Jan2021) felt like she had the flu and felt like she was hit by truck and she felt really sick. The patient goes back and forth having diarrhea on 18Jan2021. For the reported events injection site started hurting, headache, she's breathing she feel like her lungs are cold, she cannot breathe good, and feels like they (lungs) were burning, throwing up and feel nauseas, diarrhea; an ER or physician's office required and gave her Zofran. The outcome of the event injection site started hurting and headache was recovered; unknown for he has not been feeling well/not felt very good, felt like she had the flu and felt like she was hit by truck and felt really sick; and not recovered for the rest of the events.

Other Meds: AMITRIPTYLINE

Current Illness:

ID: 1000113
Sex: F
Age:
State: VA

Vax Date: 01/05/2021
Onset Date: 01/08/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Left shoulder/joint pain; left shoulder partial immobility; left hand/finger tingling; This is a spontaneous report from a contactable Nurse (patient). A 36-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EK417J, expiry date: unknown), via an unspecified route of administration from on 05Jan2021 10:30 at single dose (Left Deltoid) for COVID-19 immunization. The patient medical history was not reported. Patient is not pregnant. Patient had no covid prior vaccination, patient had no covid tested post vaccination, and no known allergies. Concomitant medication included paroxetine (PAROXETINE). The patient received first dose of bnt162b2 (lot number: PAA156051) on 12Dec2020 at Left Deltoid for COVID-19 immunization at 35 years-old. Vaccination facility type was Hospital. The patient experienced left shoulder/joint pain, left shoulder partial immobility, and left hand/finger tingling that has not gone away; all on 08Jan2021 08:00. The outcome of the events was not recovered. No treatment for events was given.

Other Meds: PAROXETINE

Current Illness:

ID: 1000114
Sex: F
Age:
State: NY

Vax Date: 01/08/2021
Onset Date: 01/18/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Mild Rash all over appear 10 days after vaccine; This is a spontaneous report from a contactable nurse (patient). A 38-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Solution for injection lot no. EH9899, expiry date: not reported), intramuscular on 08Jan2021 08:30 at a single dose (first dose) on left arm for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took cipro [ciprofloxacin hydrochloride] which she had known allergies. The patient experienced mild rash all over appear 10 days after vaccine (18Jan2021). The patient has no COVID prior vaccination and has not tested post vaccination. The COVID vaccine was administered in a hospital. She had no other vaccines received in four weeks and no treatment was received in response to the adverse event. The outcome of the event was not recovered.

Other Meds:

Current Illness:

ID: 1000115
Sex: F
Age:
State: NM

Vax Date: 12/30/2020
Onset Date: 12/30/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Feeling itchy at the injection site; Felt not okay; This is a spontaneous report from a contactable pharmacist. A 47-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: EL1284), via intramuscular (left arm) on 30Dec2020 12:15 at SINGLE DOSE for COVID-19 immunisation. Medical history included depression, Hyperlipidemia, Migraine with aura, NASH, Known allergies: penicillin from unspecified dates. The patient was not pregnant during vaccination time. Patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Concomitant medication included atorvastatin, fluoxetine, fluticasone (FLUTICASONE), omeprazole, for unspecified indications; rizatriptan for migraine, and norethisterone (MICRONOR) for Oral contraceptive, all from unspecified dates. The patient experienced feeling itchy at the injection site, and felt not okay on 30Dec2020 12:15. No SOB, lightheadedness, hives or numbness. Rapid Response was called (emergency visit) and was advised extra observation time. No other intervention. Treatment was not given. Outcome of events was recovered. Events were considered non-serious.

Other Meds: ATORVASTATIN; FLUOXETINE; FLUTICASONE; MICRONOR; OMEPRAZOLE; RIZATRIPTAN

Current Illness:

ID: 1000116
Sex: M
Age:
State: IL

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210119; Test Name: temperature; Result Unstructured Data: Test Result:99.9

Allergies:

Symptoms: flu like side effects; increased temperature (99.9); lower back pain; chills; muscle aches; This is a spontaneous report from a contactable consumer (patient himself) reported that a 33-year-old male patient received his second dose of bnt162b2 (BNT162B2 also reported as Covid vaccine, lot EL3247), via an unspecified route of administration in the left arm on 19Jan2021 09:00 at SINGLE DOSE for Covid-19 immunisation. Medical history included eosinophilic esophagitis and carry an epi-pen for gastrointestinal anaphylaxis, had food allergy to quinoa, shrimp and mango. He had his first dose of bnt162b2 on 29Dec2020 (lot EK9231,) in the left arm. Concomitant medications included pantoprazole, cetirizine hydrochloride, fluticasone propionate (FLONASE) and melatonin. On 19Jan2021 22:00, she had flu like side effects, increased temperature (99.9), lower back pain, chills, and muscle aches. She self-administered acetaminophen and ibuprofen. The outcome of event was recovered with sequelae (Recovered with lasting effects).

Other Meds: PANTOPRAZOLE; CETRIZINE; FLONASE [FLUTICASONE PROPIONATE]; MELATONIN

Current Illness:

ID: 1000117
Sex: F
Age:
State: NC

Vax Date: 01/13/2021
Onset Date: 01/15/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210115; Test Name: BP; Result Unstructured Data: Test Result:up to 86/85

Allergies:

Symptoms: Like a truck hit me a day later BP up to 86/85; Like a truck hit me a day later BP up to 86/85; This is a spontaneous report from a contactable consumer (patient). An 86-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: El 3248), via an unspecified route of administration at the right arm on 13Jan2021 at 14:00 (02:00 PM) at single dose for COVID-19 immunization, administered in a hospital. The patient's medical history included breast cancer, thyroid low, and known allergies to bee sting, shellfish, codeine and sulfur. The patient's concomitant medication included thyroid (as reported) that the patient received in two weeks. The patient had no other vaccine in four weeks. The patient had no COVID prior to the vaccination and has not tested for COVID post vaccination. The patient is not pregnant. The patient experienced "like a truck hit me a day later bp up to 86/85" on 15Jan2021 at 09:15 AM. Treatment received for the events was reported as "Emergency" (pending clarification). The outcome of the events was recovered with sequelae (reported as recovered with lasting effects).

Other Meds:

Current Illness:

ID: 1000118
Sex: M
Age:
State: PA

Vax Date: 01/14/2021
Onset Date: 01/15/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: swelling on his lower gums; sensitivity to his teeth; redness on his gums; This is a spontaneous report from a contactable physician (patient). A 67-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL1284), via intramuscular route of administration on 14Jan2021 at 12:40 at 0.3 mL, single in the deltoid left for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL0140) on 23Dec2020 at 0.3 ml IM injection for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 15Jan2021, the patient experienced swelling on his lower gums in the front of his mouth and sensitivity to his teeth, no other symptoms. The swelling gums went away, it was mild and it went away. A few hours after, there was redness on his gums, no drainage or anything and then the teeth sensitivity went away through the day. He was wondering if those things have been associated with the product or maybe just a coincidence. The patient recovered from the events swelling on his lower gums and sensitivity to his teeth on 15Jan2021 while unknown for the other event.

Other Meds:

Current Illness:

ID: 1000119
Sex: F
Age:
State:

Vax Date: 01/20/2021
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: feeling crappy; my muscles hurt; This is a spontaneous report from a contactable Other Health Professional (patient) via the Pfizer sponsored program. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiration date were not reported), via an unspecified route of administration on 20Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient had the vaccine in the morning of 20Jan2021 and she was feeling crappy and her muscles hurt in Jan2021. She stated that she read if you have Covid you should take TYLENOL instead of Ibuprofen. She was wondering if this was the same with the vaccine or if it was okay to take ibuprofen. The outcome of the events feeling crappy and my muscles hurt was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000120
Sex: F
Age:
State:

Vax Date: 01/02/2021
Onset Date: 01/07/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210107; Test Name: Covid; Result Unstructured Data: Test Result:contracted

Allergies:

Symptoms: contracted Covid 07Jan2021; contracted Covid 07Jan2021; This is a spontaneous report from a contactable other healthcare professional (patient). A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number was unknown), via an unspecified route of administration on 02Jan2021 at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient reported that she received the first dose on 02Jan2021 and contracted Covid 07Jan2021. She was out of isolation since 17Jan2021 and currently have no symptoms. She is scheduled to receive the vaccine this coming Saturday (23Jan2021). The patient wanted to know if she can receive the second dose or should she postpone her appointment. The patient asked what would happen if she decided to get the second dose in 3 months after dose 1 and asked if she would need to start the vaccine series from the beginning. The outcome of the event was recovered on Jan2021. Information on the lot/batch number has been requested.; Sender's Comments: Based on available information, a possible contributory role of the subject product, BNT162B2 vaccine, cannot be excluded for the reported events of COVID-19 and suspected LOE due to temporal relationship. There is limited information provided in this report. This case will be reassessed once additional information is 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: 1000121
Sex: F
Age:
State: NM

Vax Date: 12/30/2020
Onset Date: 12/30/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: numbness of left hand and fingers; Pain on forearm (Pressure feeling); Pain on forearm (Pressure feeling); This is a spontaneous report from a contactable pharmacist. A 43-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1284), intramuscular on 30Dec2020 at 12:30 on left arm at a single dose for COVID-19 immunisation. The patient has no medical history. The patient's concomitant medications were not reported. The patient started feeling numbness of left hand and fingers after 10 minutes (30Dec2020 at 12:40) and pain on forearm (pressure feeling) 30Dec2020 at 12:30. There was no treatment received for the events. The outcome of the events was recovered on an unspecified date.

Other Meds:

Current Illness:

ID: 1000122
Sex: F
Age:
State: NY

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: hives from the neck to legs; Face redness; tightness in the chest; unable to take a deep breathe; This is a spontaneous report from a contactable nurse. A 36-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3248), intramuscular in left arm on 12Jan2021 11:00 to at a single dose for COVID-19 immunization. Vaccination was done in a hospital. There were no relevant medical history and concomitant medications. On 12Jan2021 11:00, hives from the neck to legs, face redness and tightness in the chest, and was unable to take a deep breathe. The outcome of the events was recovered with sequelae. The events resulted in an emergency room/department or urgent care. Treatment for the events included Benadryl, Ativan, Pepcid, NS Bolus and EpiPen. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not tested with COVID-19 post vaccination.; Sender's Comments: Based on available information, a possible contributory role of the subject product, BNT162B2 vaccine, cannot be excluded for the reported events of hives from the neck to legs, face redness and tightness in the chest, and was unable to take a deep breathe due to temporal relationship. There is limited information provided in this report. Additional information is needed to better assess the case, including complete medical history, diagnostics including physical examination with vitals and chest x-ray, counteractive treatment measures and concomitant medications. This case will be reassessed once additional information is 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: 1000123
Sex: F
Age:
State: NM

Vax Date: 12/23/2020
Onset Date: 12/23/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: perioral numbness with HA; perioral numbness with HA; Difficulty swallowing & breathing; Difficulty swallowing & breathing; This is a spontaneous report from a contactable pharmacist. A 50-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1284 and expiration date not provided), intramuscular in the left arm on 23Dec2020 09:45 at a single dose for COVID-19 immunization. Medical history included hypothyroidism and allergies to garlic. The patient is not pregnant. The patient did not receive any other vaccine within 4 weeks prior to the COVID vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medication included levothyroxine sodium. The patient previously took sulfamethoxazole trimethoprim (BACTRIM) and experienced allergies. On 23Dec2020 09:45, the patient experienced perioral numbness with HA, Difficulty swallowing and breathing. The patient felt it was likely due to the N95 mask. She was given procedural mask and reported improvement of symptoms. A Rapid response was contacted. No other intervention was done. Treatment was not provided in response to the events. The outcome of the events was recovered on an unspecified date. The patient has not tested for COVID post vaccination.

Other Meds: LEVOTHYROXINE SODIUM

Current Illness:

ID: 1000124
Sex: F
Age:
State:

Vax Date: 01/15/2021
Onset Date: 01/16/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Name: she was tested; Result Unstructured Data: Test Result:Unknown result; Test Date: 20210117; Test Name: O2 saturation; Result Unstructured Data: Test Result:between 86-88; Test Date: 20210117; Test Name: O2 saturation; Result Unstructured Data: Test Result:86; Test Date: 20210117; Test Name: pulse; Result Unstructured Data: Test Result:133; Comments: rapid pulse; Test Name: Fever; Result Unstructured Data: Test Result:100 Fahrenheit; Comments: greater fever than 100; Test Date: 20210117; Test Name: breathing; Result Unstructured Data: Test Result:94

Allergies:

Symptoms: the thermometer that marked 100?F orally (she says that the fever was higher in the night); States she is shrinking. Weight varies; cough; 86 of oxygen saturation/O2 saturation was anywhere between 86-88; pulse was 133/rapid pulse, it was 133/rapid heartbeat; her breathing was above 94; shooting pain/stabbing pain at the injection site/extremely excruciating stabbing pains in her arm with the shot; shivers; headache/splitting headache; freezing; slight breathing difficulty; slight body aches; Sore arm; Fatigue; This is a spontaneous report from a contactable consumer. A 73-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot EL1284, expiration date unspecified), via an unspecified route of administration on 15Jan2021 at single dose (left arm) for COVID-19 immunization. Medical history included high blood pressure diagnosed 15 years ago, maybe; High cholesterol diagnosed 20 years ago, she doesn't know, reflux diagnosed 20 years ago, maybe more, prediabetes and allergy induced asthma which she carries an inhaler, and she has used it maybe three times a year. Patient reported that she was tested and they don't know for sure, but she reported that she may have allergy induced asthma as she has to take, carries an inhaler, and she has used it maybe three times a year, in the fall when leaves are falling down, the leaves get moldy, and she was driving in her car, or walking in a wooded area, she gets tightness, takes her inhaler and was fine, that's the extent, no other circumstances; fall or she had where a plant was blooming outdoors, she gets tightness, and she took her inhaler, and was good for the next year, so sitting in the environment and nothing further materializes, if she takes the inhaler three or two times a year, considering what other people have, she thought this was insignificant. There were no concomitant medications. The patient reported that she got vaccinated this Friday and had nothing but a sore arm afterwards, on 16Jan2021 and was fine all day, evening, all day Saturday. She just had soreness at the site, she had no redness at the site of injection, but the weird part: she doesn't think anyone would believe, 33 hours later, at midnight, she was still up, on her way to bed, and all of a sudden she experienced extremely excruciating stabbing pains in her arm with the shot, it was stabbing, excruciating, and immediately at the same time, she had shivers/shivered and had a splitting headache, was freezing and had to put socks on, and had noticed very slight difficulty breathing, and since it was midnight, she didn't want to wake up her husband, she dozed off, and was up at 0530. She had body aches, slight, it was the least, but the stabbing stopped in her arm. She slept from 12:30 to 05:30, and the shivering and aches stopped, but the headache was still on, so she took a pill for the headache. She took the thermometer that marked 100F orally; she stated that the fever was higher in the night and she assumed with the shivering, she had a greater fever than 100. Also, the oximeter indicated 133 pulse and 86 of oxygen saturation. By 10:00, it all had resolved. She has an oximeter, and since she still had the feeling of difficulty breathing, she put it on, but her pulse was 133, that was when she was feeling better. It was reported that all symptoms were gone except for rapid pulse, it was 133 and the slight breathing, and her 02 saturation was anywhere between 86-88, it varied, and by 10:00, all issues resolved, her heartbeat was down to normal, her breathing was above 94, or whatever, everything was fine, and has been fine since then. Maybe she had fatigue on Saturday and Sunday, on Sunday was like after the flu, after you finish, you have fatigue and was a little out of it, this was on Sunday. On an unspecified date, the patient stated that she was shrinking and weight varies. Patient stated that the only thing she does have, says she has a cough, but because she needs a drink, she was not sick and she gets to drink water. She felt like the reaction she had was in the limit of a severe allergic reaction due to the rapid heartbeat and her difficulty breathing. She would like to know if there was information about these side effects reported so she can determine if she was going to have the second dose of the vaccine. Outcome of events states she was shrinking, weight varies and cough was unknown; and outcome of the rest of events was recovered on an unspecified date.

Other Meds:

Current Illness:

ID: 1000125
Sex: F
Age:
State: PA

Vax Date: 01/16/2021
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headache; diarrhea; nausea; lethargy; This is a spontaneous report from a contactable other healthcare professional (hcp reported for self). A 43-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot EK9231, expiry date not reported), via an unspecified route of administration on 16Jan2021 15:00 at a single dose for COVID-19 immunization. Medical history included known allergies to poultry and egg. The patient was not pregnant at the time of the vaccination. The patient had no COVID prior to vaccination. Concomitant medications included ethinylestradiol, norethisterone (CYCLAFEM 0.5/35), riboflavin (VIT B2), colecalciferol (D3), magnesium, and bifidobacterium lactis (PROBIOTIC); all reported as other medications in two weeks. Patient had no other vaccine in four weeks. On an unspecified date in Jan2021 (also reported as 03Jan2021; pending clarification), the patient experienced headache, diarrhea, nausea, and lethargy continued after 4 days. No treatments received in response to the events reported. The patient was not tested for COVID post vaccination. The events headache, diarrhea, nausea, and lethargy were not recovered.

Other Meds: CYCLAFEM 0.5/35; VIT B2; D3; MAGNESIUM; PROBIOTIC [BIFIDOBACTERIUM LACTIS]

Current Illness:

ID: 1000126
Sex: F
Age:
State: NC

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headaches; pain/extreme body aches (worse than my fibromyalgia); a little difficulty to breath; extreme tiredness; swelling; woke up with my face swollen it went down after hot shower; Nauseous throughout the day; eyes burning; cold sores on my mouth; This is a spontaneous report from a contactable health care professional nurse, the patient. A 50-year-old non-pregnant female patient (health care professional) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot Number: EL3248), in the right arm on 19Jan2021 13:15 as a single dose, for COVID-19 vaccination. The vaccine was administered at a Public Health Clinic facility. Medical history included asthma, Fibromyalgia and known drug allergy to penicillin. Concomitant medication included diclofenac (DICLOFENAC), clonazepam (KLONOPIN). No other vaccines were given within 4 weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination the patient had not been tested for COVID-19. On 19Jan2021 20:00, the patient experienced pain started at exactly 8:00pm; extreme body aches (worse than my fibromyalgia), a little difficulty to breath, extreme tiredness, swelling, woke up with my face swollen (it went down after hot shower). Nauseous throughout the day, eyes burning and cold sores on my mouth and Headaches. No treatment was received given for the event. The clinical outcome of pain, extreme body aches, difficulty to breath, extreme tiredness, swelling, face swollen, nauseous, eyes burning, cold sores on mouth and Headaches were recovering.

Other Meds: DICLOFENAC; KLONOPIN

Current Illness:

ID: 1000127
Sex: F
Age:
State: CA

Vax Date: 01/10/2021
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: pain and numbness on left forearm near the injection site; pain and numbness on left forearm near the injection site; mild hypertension; tachycardia; This is a spontaneous report from a contactable pharmacist. A 46-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number EL3249 and expiry date unknown) intramuscular at the left arm on 10Jan2021 at single dose for Covid-19 immunization in a hospital. Medical history was none. It was unknown if the patient was pregnant. The patient had no covid prior vaccination. The patient's concomitant medications were not reported. The patient had no other vaccine in four weeks. In Jan2021, the patient experienced pain and numbness on left forearm near the injection site, mild hypertension and tachycardia. The patient was not covid tested post vaccination. The patient did not receive treatment due to the events. The outcome of the events pain and numbness on left forearm near the injection site was recovered in Jan2021, while mild hypertension and tachycardia was unknown.

Other Meds:

Current Illness:

ID: 1000128
Sex: F
Age:
State: FL

Vax Date: 01/18/2021
Onset Date: 01/18/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: felt confused/ sent emails and text which were very abnormal and confusing. Not making lots of sense; I was tired; mild headache; neck pain; acutely drowsy; completed several notes and had no memory of completing the notes at all; Unable to fall asleep to pain; Unable to fall asleep to pain; 1st dose of BNT162B2 on 23Dec2020/ received the second dose on 18Jan2021; This is a spontaneous report from a contactable other healthcare professional (patient). A 37-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EL3246) via an unspecified route of administration on the right arm on 18Jan2021 13:00 at a single dose for COVID-19 immunisation. Medical history included migraine headaches and depression. The patient's concomitant medications were not reported. The patient previously received 1st dose of BNT162B2 on 23Dec2020 for COVID-19 immunisation (lot number EJ1685, right arm). On 19Jan2021 19:45, the patient felt confused, thought she was tired and was trying to push through and write notes, she knew something wasn't quite right. She experienced mild headache and neck pain. I was making a lot of errors while writing notes and I was aware. This night I also sent emails and text which were very abnormal and confusing. Not making lots of sense. I received text asking me "what?" Because what she was sending made no sense. She was acutely drowsy and fell asleep mid text. She woke up mid morning with severe neck pain unable to touch chin to chest. Unable to fall asleep to pain. Took Tylenol and muscle relaxer. Went to work as PA. She forgot she had written notes night before. Thinking notes were not complete logged into hospital to write notes and she completed several notes and had no memory of completing the notes at all. No treatment was received for the events. Events were reported as non-serious. Patient was not pregnant. The facility where the vaccine was administered was in a hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, the patient has not been tested for COVID-19. Prior to vaccination, the patient was not diagnosed with COVID-19. No allergies to medications, food, or other products. Outcome of the event mild headache was resolved on 21Jan2021, neck pain was recovering, while unknown for the other events.

Other Meds:

Current Illness:

ID: 1000129
Sex: M
Age:
State: AZ

Vax Date: 01/19/2021
Onset Date: 01/20/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210120; Test Name: body temperature; Result Unstructured Data: Test Result:103.7; Comments: high fever after 2nd dose

Allergies:

Symptoms: High fever after 2nd dose (103.7); This is a spontaneous report from a contactable pharmacist(patient). A 32-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number:ELI283), via an unspecified route of administration into the left arm on 19Jan2021 09:30 at a single dose for covid-19 immunisation. Medical history was reported as none. Concomitant medication included amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL) and gabapentin (GABAPENTIN). The patient was previously administered with first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number:EH9899), via an unspecified route of administration into the left arm on 29Dec2020 11:00 AM at a single dose for covid-19 immunization. The patient experienced high fever after 2nd dose (103.7; units unspecified) on 20Jan2021 03:00. The event was reported as non-serious and the patient did not receive treatment. Outcome of event recovered on an unspecified date.

Other Meds: ADDERALL; GABAPENTIN

Current Illness:

ID: 1000130
Sex: F
Age:
State: TN

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

Lab Data: Test Name: fever; Result Unstructured Data: Test Result:99.4; Comments: low grade fever 99.4 orally

Allergies:

Symptoms: Chills; low grade fever 99.4 orally; fatigue; weakness; This is a spontaneous report from a contactable Physician. A 77-year-old female received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Solution for injection, lot no. and expiry date not reported), via an unspecified route of administration on an unspecified date at single dose (2nd dose) for covid-19 immunization. Medical history included high cholesterol and has no known allergies. The patient's concomitant medications were not reported. The patient had her first dose on left arm of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE lot no. EJ1685) at 12:00 on 22Dec2020 but had slight discomfort site injection and occasional soreness site injection over the subsequent 3 weeks. For vaccine dose 2, it was reported that after 30-36 hr, patient developed chills, low grade fever 99.4 orally, fatigue, weakness and took ibuprofen. She slept normal by 42 hrs and no further complications. The outcome of events recovered on unspecified date. The facility where the most recent COVID-19 vaccine was administered was in a school clinic. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000131
Sex: M
Age:
State: MN

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

Lab Data:

Allergies:

Symptoms: Arm soreness site starting on 12th hour to 36th hr post the 1st dose; This is a spontaneous report from a contactable nurse. A male patient of an unspecified age (reported as age: 37, unit: unspecified) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiry date not reported), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient had 1st dose of COVID 19 vaccine on an unspecified date and that the only thing he experienced was "arm soreness site starting on 12th hour to 36th hr (hour) post the 1st dose". The outcome of the event arm soreness site was unknown. No follow up attempts are possible. Information about Lot and batch number could not be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1000132
Sex: F
Age:
State: IN

Vax Date: 01/18/2021
Onset Date: 01/18/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: pain at the injection site, left arm; so stressed; This is a spontaneous report from a contactable consumer, the patient. A 72-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot EK9231) solution for injection intramuscular in the left arm on 18Jan2021 at 15:00 (at the age of 72-years-old) as a single dose for COVID-19 vaccination. Medical history included allergic to sulfa. Concomitant medications were not reported. Past drug history included drug allergy: ciprofloxacin (CIPRO) and codeine. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. On 18Jan2021, the patient experienced pain at the injection site, left arm and so stressed. There was no emergency room or physician office visit. No treatment was provided for event pain at the injection site. The outcome of the event pain at the injection site was not recovered. The outcome of the event stressed was unknown.

Other Meds:

Current Illness:

ID: 1000133
Sex: M
Age:
State:

Vax Date: 12/31/2020
Onset Date:
Rec V Date: 02/04/2021
Hospital:

Lab Data: 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 pharmacist. This pharmacist reported similar events for two patients. This is the first of the two reports. A 70-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 31Dec2020 at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. This patient was vaccinated and has tested positive for Covid-19 on an unspecified date, not sure when he tested positive for the Covid-19. He was asymptomatic. It was also reported that he got sick on 03Jan2021. The second dose is due 21Jan2021, is it ok for him to receive it? How long can he wait if he does not get the vaccine at 21 days? The outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Based on the information currently available, lack of efficacy of the suspected vaccine BNT162B2 cannot be completely excluded. However, individuals may not be protected until at least 7 days after their second dose of the vaccine. It is unlikely that the patient would have fully developed immunity due to the very short time lag between the first vaccine dose and the event onset.,Linked Report(s) : US-PFIZER INC-2021035296 same reporter/product, similar events and different patient

Other Meds:

Current Illness:

ID: 1000134
Sex: F
Age:
State: KS

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

Lab Data: Test Date: 20210118; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: rashes on arm getting worse and had one on chest and then on legs; I felt like I was gonna pass out and I did it right when I got to my house; I felt like I was gonna pass out and I did it right when I got to my house; She was lightheaded and extremely dizzy; huge headache; arm didn't hurt when she got the shot but 30 minutes later it hurt so bad; throat hurt extremely bad; This is a spontaneous report from a contactable health professional, the patient. A 19-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), intramuscularly in the left arm on 11Jan2021 at 15:00 (at the age of 19-years-old) as a single dose for COVID-19 immunization. Medical history included allergies to latex, oranges, and adhesive. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included amfetamine aspartate/amfetamine sulfate/dexamfetamine saccharate/dexamfetamine sulfate (ADDERALL), hydroxyzine and celecoxib (CELEXA). The patient did not receive any other vaccines within 4 weeks prior to the vaccination. Her arm didn't hurt when she got the shot but 30 minutes later, on 11Jan2021 at 15:30, it hurt so bad. On 18Jan2021 at 15:00 (also reported as the Monday of the vaccination), the patient experienced a feeling like she was going to pass out, at cheer practice, and did it right when she got to her house. She was lightheaded and extremely dizzy the whole time at practice and had a huge headache. Also, when she got to practice at on 18Jan2021 at 15:15, she noticed the rashes on her arm getting worse, and on her chest and then on her legs. Then, on an unknown date in Jan2021, her throat hurt extremely bad, so she gargled with salt water and it felt a little better. The patient was not treated for the events "I felt like I was gonna pass out and I did it right when I got to my house", "She was lightheaded and extremely dizzy", "huge headache", "rashes on arm getting worse and had one on chest and then on legs" and "arm didn't hurt when she got the shot but 30 minutes later it hurt so bad"; and was treated for "throat hurt extremely bad" as the patient gargled with salt water. Since the vaccination, the patient had been tested for COVID-19 via rapid nasal swab on 18Jan2021 with a negative result. The clinical outcome of "I felt like I was gonna pass out and I did it right when I got to my house" and "arm didn't hurt when she got the shot but 30 minutes later it hurt so bad" was unknown; of "She was lightheaded and extremely dizzy", "huge headache", "rashes on arm getting worse and had one on chest and then on legs", "throat hurt extremely bad" was resolving. Information on the lot/batch number has been requested.; Sender's Comments: Considering the temporal association, a causal association between administration of BNT162B2 and the onset of pass out cannot be fully excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate. 40.~

Other Meds: ADDERALL; HYDROXYZINE; CELEXA

Current Illness:

ID: 1000135
Sex: M
Age:
State: NY

Vax Date: 12/01/2020
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Dizziness; vertigo; nausea; headache; This is a spontaneous report from a contactable physician reporting for himself. A 69-year-old male patient received the first single dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number EK5730, expiry date not reported) on an unspecified date in Dec2020 12:45 via an unspecified route of administration in the left arm, and the second single dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (lot number EL3246, expiry date not reported) on 11Jan2021 13:30 via an unspecified route of administration in the left arm, for COVID-19 immunization. Medical history included penicillin allergy, mild hypothyroidism, gastrooesophageal reflux disease (GERD) and benign prostatic hyperplasia (BPH), unspecified if ongoing. Concomitant medication included levothyroxine sodium (LEVOTHYROXINE), famotidine, dutasteride, from an unspecified date to an unspecified date (received in two weeks, as reported); simvastatin, tadalafil, herbal pollen nos/quercetin (PROSTATE PQ), and "Supplements Prostagenix", from an unspecified date and ongoing. The patient had not had COVID piror to the vaccination, and had not tested post the vaccination. The patient experienced dizziness/vertigo with nausea and headache beginning 1-2 weeks (unspecified date in Jan2021) after the initial vaccination and worse after the second dose. The events resulted in doctor or other healthcare professional office/clinic visit. The patient received scopolamine 1mg/3 day patch x 5 for the events. The events were not resolved.

Other Meds: LEVOTHYROXINE [LEVOTHYROXINE SODIUM]; FAMOTIDINE; DUTASTERIDE; SIMVASTATIN; TADALAFIL; PROSTATE PQ

Current Illness:

ID: 1000136
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Fatigue; Massive headache; Aches; Fever; This case has been considered invalid: no first-hand knowledge of adverse events This is a spontaneous report from a non-contactable consumer. This consumer reported for a 44-year-old female patient that: I learned from a friend yesterday that her friend had told her through text message that she experienced side effects as a result of the second dose of the Pfizer COVID 19 vaccine. As an employee of Pfizer, I know it is my responsibility to report side effects and learned of these during a meal. The report came up during conversation. The patient, 44 you F, received Pfizer vaccine at her work and reported the following side effects via text message: "Felt great after first dose, second dose, rough, fever, aches, massive headache, fatigue." No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1000137
Sex: F
Age:
State: CA

Vax Date: 12/22/2020
Onset Date: 12/23/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20201223; Test Name: Fever; Result Unstructured Data: Test Result:99.9; Comments: 08:00

Allergies:

Symptoms: Fever 99.9; body aches; Injection site tenderness, swelling, redness x 10 days; Injection site tenderness, swelling, redness x 10 days; Injection site tenderness, swelling, redness x 10 days; This is a spontaneous report from a contactable nurse (patient). A 27-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK5730) via an unspecified route of administration at left arm, on 22Dec2020 10:15 at single dose for covid-19 immunisation. Medical history included having COVID prior vaccination. Patient has no known allergies. Patient is not pregnant. Concomitant medications included cetirizine hydrochloride (ZYRTEC), vitamins nos (MULTIVITAMIN). Patient did not receive other vaccine in four weeks. Patient experienced fever 99.9, body aches, Injection site tenderness, swelling, redness x 10 days, all on 23Dec2020 08:00. No treatment received for events. Patient did not test COVID post vaccination. Outcome of the events was recovered.

Other Meds: ZYRTEC [CETIRIZINE HYDROCHLORIDE]; MULTIVITAMIN [VITAMINS NOS]

Current Illness:

ID: 1000138
Sex: F
Age:
State: VA

Vax Date: 01/15/2021
Onset Date: 01/15/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210118; Test Name: fever; Result Unstructured Data: Test Result:99.1 Fahrenheit; Test Date: 20210119; Test Name: fever; Result Unstructured Data: Test Result:98.9 Fahrenheit; Test Date: 20210119; Test Name: COVID-19 PCR test negative; Result Unstructured Data: Test Result:Negative

Allergies:

Symptoms: fever 99.1 Fahrenheit; shivers and chills; shivers and chills; body aches; Headache; dull chest pain; Fatigue; Injection site pain; This is a spontaneous report from a contactable consumer, the patient. A 43-years-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: EK4176), via an unspecified route of administration, in the left arm on 15Jan2021 at 08:50 AM (at the age of 43-year-old) as a single dose for COVID-19 immunization. Medical history was none. There were no concomitant medications. The patient did not receive any other vaccines within four weeks prior to the vaccination On 15Jan2021, the patient experienced injection site pain. On 18Jan2021, the patient experienced fever 99.1 Fahrenheit, shivers and chills, body aches, headache, dull chest pain, fatigue,. The patient had lab tests which included: 18Jan2021: pyrexia: 99.1 Fahrenheit, 19Jan2021: pyrexia: 98.9 Fahrenheit. Treatment for the body aches included with Theraflu, and ibuprofen liquids for the headache. The clinical outcome of the event injection site pain was recovered on 16Jan2021, fever 99.1 Fahrenheit, and dull chest pain was recovered on 19Jan2021, shivers and chills was recovered on 20Jan2021. The clinical outcome of the body aches, headache, fatigue, was not recovered. It was also reported that since the vaccination, the patient had been tested for COVID-19 on 19Jan2021, the results of which was negative.

Other Meds:

Current Illness:

ID: 1000139
Sex: F
Age:
State:

Vax Date: 01/14/2021
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: My throat is very muffled, like a sore throat but it doesn't hurt; weakness; I woke up dizzy like I have vertigo/dizziness; I work the night shift from 11-7/Yesterday morning (come home from work), I was wide awake, fell asleep at 4pm; My throat is very muffled, like a sore throat but it doesn't hurt; I woke up dizzy like I have vertigo; My throat is like I have a frog in my throat; my arm was sore; upset stomach; This is a spontaneous report received from a contactable other healthcare professional (patient). A female patient of an unspecified age (reported as 53, unit not provided, pending clarification) 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 14Jan2021, at single dose, for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Historical vaccine included 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, for COVID-19 immunization for which the patient experienced upset stomach, cried al day/cried event at work for a whole 24 hours/crying for no reason like she was depressed. The patient stated, "I received the second shot Thursday morning (14Jan2021), I went to work (I work the night shift from 11-7). I was fine; my arm was sore. I had an upset stomach. On 15Jan2021, yesterday morning (come home from work), I was wide awake and fell asleep at 4pm. I woke up dizzy like I have vertigo. My throat is like I have a frog in my throat. The dizziness and weakness, since 9pm last night (15Jan2021). My throat is very muffled, like a sore throat but it doesn't hurt. I have dizziness. I knew there were side effects to the shot. ". The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000140
Sex: M
Age:
State: FL

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210115; Test Name: blood draw; Result Unstructured Data: Test Result:dehydration; Test Date: 20210115; Test Name: urine analysis; Result Unstructured Data: Test Result:Bloody urine/blood cells and bilirubin in urine

Allergies:

Symptoms: Bloody urine; UA indicated red blood cells and bilirubin in urine; UA indicated red blood cells and bilirubin in urine; Basic Metabolic Panel indicated dehydration; Dose Number 1, Date of start of drug (21Dec2020) / Dose Number 2, Date of start of drug (13Jan2021); Dose Number 1, Date of start of drug (21Dec2020) / Dose Number 2, Date of start of drug (13Jan2021); This is a spontaneous report from a contactable pharmacist. This 32-year-old male pharmacist (Patient) reported for himself that he received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number= EL1284), via unspecified route at left arm on 13Jan2021 10:00am at single dose for COVID-19 immunization. Medical history was not reported. Concomitant drugs included Vitamin D3. Historical vaccine included the first dose of BNT162B2 (lot number= EH9899) on 21Dec2020 02:30 pm at left arm for COVID-19 immunization. Facility type vaccine was hospital. No other vaccine in four weeks. On 15Jan2021 01:30 pm, patient had bloody urine, he was otherwise normal health, he visited healthcare provider within 3 hours of the incident. Point of care urine analysis (UA) and blood draw was done. UA indicated red blood cells and bilirubin in urine. Basic Metabolic Panel indicated dehydration, otherwise unremarkable. Events resulted in emergency room/department or urgent care. No treatment was received. Outcome of events was recovered in Jan2021. No COVID prior vaccination. No COVID tested post vaccination.

Other Meds: VITAMIN D3

Current Illness:

ID: 1000141
Sex: F
Age:
State: DE

Vax Date: 01/07/2021
Onset Date: 01/07/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: 2 hours after receiving vaccine, I became itchy all over body and could not stop. My head, legs, arms, ears, eyes, up my nose, etc were itchy.; I did not have hives., just redness from scratching non stop; I did not have hives., just redness from scratching non stop; This is a spontaneous report from a contactable nurse (patient). A 37-year-old female patient (not pregnant) received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine, Lot Number EL3248 and Expiration Date unknown) via Intramuscular on 07Jan2021 12:30 PM (vaccine location: Arm Left) at single dose for COVID-19 immunisation. The patient's medical history was reported as Endometreosis, Polycystic ovary (PCOS), anxiety and known allergies to Penicillin. The concomitant medications included duloxetine hydrochloride (CYMBALTA), topiramate (TOPAMAX), Spironolactone, Gabapentin, cetirizine hydrochloride (ZYRTEC), birth control. 2 hours after receiving vaccine on 07Jan2021 02:30 PM, patient became itchy all over body and could not stop. Her head, legs, arms, ears, eyes, up nose, etc were itchy. Patient did not have hives, just redness from scratching non stop, she went home and took Benadryl 50mg, and was still itchy, but not constantly. On 08Jan2021, patient was still itchy all day, but only needed 25 mg of Benadryl to help symptoms and it wasn't nearly as bad as day before. By 09Jan2021, the itching was gone. The outcome of event was recovered on 09Jan2021.

Other Meds: CYMBALTA; TOPAMAX; SPIRONOLACTONE; GABAPENTIN; ZYRTEC [CETIRIZINE HYDROCHLORIDE]

Current Illness:

ID: 1000142
Sex: M
Age:
State: FL

Vax Date: 01/09/2021
Onset Date: 01/10/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: temperature; Result Unstructured Data: Test Result:102

Allergies:

Symptoms: terrible headache lasting 3 days after injection; elevated temperature on day 2 of 102; sore and red arm at injection site; sore and red arm at injection site; body aches; This is a spontaneous report from a contactable Consumer. A 78-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number PFREL3246), via an unspecified route of administration on 09Jan2021 11:00 at single dose for covid-19 immunisation. Medical history included COPD, Asthma, Atrial Fib, Hypertension, covid-19. The patient previously took levaquin and underwent allergies:Levaquin. The patient experienced body aches, elevated temperature on day 2 of 102, sore and red arm at injection site, terrible headache lasting 3 days after injection. No treatment received. No Covid tested post vaccination. The outcome of the events was resolved.

Other Meds:

Current Illness:

ID: 1000143
Sex: M
Age:
State: CA

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

Lab Data:

Allergies:

Symptoms: elbow pain; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: unknown), 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 reported he experienced elbow pain from his vaccine on an unspecified date. The outcome of event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000144
Sex: M
Age:
State: FL

Vax Date: 12/30/2020
Onset Date: 01/15/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: He will get his second dose on 30Jun2021; Pain in the back of his neck going up towards his head; Pain in the back of his neck going up towards his head; This is a spontaneous report from a contactable consumer (patient himself). A 90-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# EL3249), via an unspecified route of administration on 30Dec2020 in right arm at single dose for covid-19 immunisation. Medical history included none. Patient just took his regular medications. Caller said that he had his vaccine done on 30Dec2020 and two days ago (15Jan2021) he started to get pain in the back of his neck going up towards his head. He has had no other problems. It could be he had been sitting too long from watching TV most of the day. But he wanted to mention this. It started a little bit on Friday 15Jan2021, then a lot on Saturday 16Jan2021, and then today it started to go up towards his head. When he bended down more and moved around it would go away for a while, then come back. He would move it back and fourth and down and up. Then it would feel good. But then if he touched it, he can feel the pain. He thought it would get better. This was his first dose. He will get his second dose on 30Jun2021. Outcome of pain in the back of his neck going up towards his head was not recovered.

Other Meds:

Current Illness:

ID: 1000145
Sex: M
Age:
State: TN

Vax Date: 01/15/2021
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: very fatigued a few hours after the vaccination; He had a very large abnormal headache; He thinks he had a fever; His arm hurt; This is a spontaneous report from a non-contactable consumer (patient). A 31-year-old male patient 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 15Jan2021 at a single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient previously received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. After his second dose of the Pfizer vaccine, the patient became very fatigued a few hours after the vaccination. He had a very large abnormal headache. He thinks he had a fever. His arm hurt. The start date of events was on an unspecified date in Jan2021. No treatment received for the events. The outcome of the events was recovered on an unspecified date in Jan2021. Facility type vaccine was Workplace clinic. Unknown if other vaccine in four weeks. Not diagnosed with COVID prior vaccination. Unknown if COVID tested post vaccination. No follow-up attempts are possible; Information on lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1000147
Sex: F
Age:
State: MI

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: go to the bathroom, remember wiping and them my husband standing over me on the floor; Sweating profusel; Product use for unapproved combination; This is a spontaneous report from a contactable consumer (patient). This 72-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number EL3249) via an unspecified route of administration in the right arm on 19Jan2021 at 09:15 at single dose for COVID-19 immunisation. The patient was not pregnant. She received another vaccine (unspecified) in the left forearm on the same date of BNT162B2. Relevant medical history included allergies to tape and potential basal cell cancer. Concomitant medications included melatonin and multi vitamins. The patient previously received varicella zoster vaccine rge (cho) (SHINGRIX) on 21Dec2020, second dose in the left arm. The patient reported that she felt great after the shot at 9:30 am on 19Jan2021 and, at 13:30, she had a potential basil cell cancer removed, and she felt great. On 20Jan2021, at 1:55 am, she got up to go to the bathroom, she remembered wiping and then her husband standing over her on the floor. On 20Jan2021 at 01:45 am, she was sweating profusely; after a minute, she got herself off the floor, back in bed, and she had no feelings of any illness. The patient did not receive corrective treatments for the reported events. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, she has not been tested for COVID-19. The patient recovered from the events on an unspecified date.

Other Meds: MELATONIN

Current Illness:

ID: 1000148
Sex: M
Age:
State: NY

Vax Date: 01/20/2021
Onset Date: 01/21/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Upper arm pain, mild; muscular discomfort, mild; This is a spontaneous report from a contactable consumer, the patient. A 47-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot EL3247) solution for injection intramuscular in the left arm on 20Jan2021 at 13:45 (at the age of 47-years-old) as a single dose for COVID-19 vaccination. There was no medical history. There were no concomitant medications. There were no allergies to medications, food, or other products. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. On 21Jan2021 at 13:45, the patient experienced upper arm pain, mild with associated muscular discomfort, mild. No treatment was provided for the events upper arm pain and muscular discomfort. The outcome of the events upper arm pain and muscular discomfort was recovering. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1000149
Sex: F
Age:
State:

Vax Date: 12/22/2020
Onset Date: 01/10/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210110; Test Name: COVID; Test Result: Positive

Allergies:

Symptoms: Covid-19 (confirmed by positive COVID-19 test); Covid-19 (confirmed by positive COVID-19 test); This is a spontaneous report from a contactable consumer, the patient. A 54-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: UNKNOWN), via an unspecified route of administration, on 22Dec2020 (at the age of 54-year-old) as a single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient reported that she received the first vaccine 22Dec2020. On 10Jan2021, she got COVID-19 and was due to get second shot 2 days later on 12Jan2021. The patient underwent lab tests which included sars-cov-2 test: positive on 10Jan2021. The patient inquired about how long to wait before the second dose after being diagnosed with COVID after receiving the first dose. The clinical outcome of the event COVID-19 was unknown. The batch/lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1000150
Sex: U
Age:
State:

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

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

Allergies:

Symptoms: tested positive 6 days after receiving vaccine; tested positive 6 days after receiving vaccine; This is a spontaneous report from a contactable consumer via a Pfizer-sponsored program Pfizer First Connect. A patient of unspecified age and gender 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 tested positive 6 days after receiving vaccine on an unspecified date. 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 about the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1000151
Sex: F
Age:
State: OH

Vax Date: 01/07/2021
Onset Date: 01/07/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Eye twitching; This is a spontaneous report from a contactable Other HCP (patient). This 29-year-old female patient (no pregnant) received 1st dose of BNT162B2 Intramuscular on 07Jan2021 02:00 PM at single dose on Right arm for covid-19 immunization. Medical history was COVID prior vaccination. No other vaccine in four weeks. Concomitant drug was not reported. Patient experienced Eye twitching on 07Jan2021 04:00 PM. No treatment. Outcome of the event was Not Recovered. No COVID tested post vaccination. No follow-up attempts are possible; information about batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1000152
Sex: F
Age:
State: AZ

Vax Date: 01/02/2021
Onset Date: 01/03/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: small red itchy bumpy rash on chest and arms; small red itchy bumpy rash on chest and arms; small red itchy bumpy rash on chest and arms; This is a spontaneous report from a contactable nurse (patient). A 58-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot EL1284) via an unspecified route of administration in the right arm on 02Jan2021 at a single dose as Covid vaccine. Medical history included hypothyroid. The patient had no known allergies. Concomitant medication included thyroid (ARMOUR THYROID) (other medications in two weeks). The patient had no other vaccine in four weeks. It was reported that the next day after receiving the vaccine, the patient developed a small red itchy bumpy rash on chest and arms on 03Jan2021. Treatment was not received for the events. She had no Covid prior to vaccination. She did not have Covid tested post vaccination. The outcome of the events was recovered with sequelae (reported as recovered with lasting effects) on Jan2021.

Other Meds: ARMOUR THYROID

Current Illness:

ID: 1000153
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: got ill for 2 days after the second dose of the vaccine; This is a spontaneous report from a Pfizer Sponsored Program, received by a contactable consumer (patient's sister). A 70-year-old female patient received the 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on unknown date at single dose for COVID-19 immunization. No relevant medical history and concomitant medications were provided. The patient was not sure if it was Pfizer or Moderna. The patient had received the 2 doses of the COVID-19 Vaccine 3 weeks apart. The patient was ill for 2 days after receiving the 2nd dose of the COVID-19 Vaccine, and then was fine. The patient had recovered from the event on unknown date. No follow-up attempts are possible. No further information is expected. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1000154
Sex: U
Age:
State: AL

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

Lab Data:

Allergies:

Symptoms: fatigue; sore arm; This is a spontaneous report from a contactable nurse. A patient of unspecified age (reported as 59 unknown unit) and gender received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), via an unspecified route of administration from an unspecified date at single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. On an unspecified date, the patient experienced fatigue and sore arm. Clinical 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: 1000155
Sex: F
Age:
State: FL

Vax Date: 01/07/2021
Onset Date: 01/15/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210118; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: Light headed; lack of appetite; achy; nauseous; sick feeling; This is a spontaneous report from a contactable consumer (Patient). A 73-Year-old female patient received first dose BNT162B2 (Pfizer BioNTech Covid 19 vaccine, lot number EH9899), via an unspecified route of administration at Arm Right on 07Jan2021 10:30 at the 73 years old at single dose for COVID-19 immunization. The medical history was none. The concomitant medications were vitamin C (ascorbic acid), atorvastatin (strength 5 mg), valsartan (strength 80 mg). There was no other vaccine in four weeks. On15Jan2021 08:00 the patient experienced Light headed, lack of appetite, achy, nauseous, sick feeling. The events were continuing though lighter for at least another 3 days. There was no treatment received for all the adverse events. The patient had no Covid prior vaccination. There was covid tested post vaccination. The patient underwent lab tests and procedures, which included Nasal Swab negative on 18Jan2021. The outcome of the events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: VITAMIN C [ASCORBIC ACID]; ATORVASTATIN; VALSARTAN

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm