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: 1056538
Sex: F
Age:
State: PA

Vax Date: 01/21/2021
Onset Date: 01/22/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: the room was spinning/whole room was spinning; dizzy spells/more of when she is in a certain position like when she is reaching up to get something or bending down, or at night when she reclines or is switching from side to side; her scalp was itching and her back and stomach was itching; This is a spontaneous report received from a contactable consumer (patient). A 50-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration on the left arm, on 21Jan2021 15:00, at single dose, for COVID-19 immunization. There were no medical history and concomitant medications. On 21Jan2021 at 15:00 (last Thursday), the patient received the first dose. On 22Jan2021 (the day after the vaccine) at 07:00, her scalp was itching and her back and stomach was itching and that went away the same day. In the morning of 23Jan2021 (also reported as "either 22Jan2021 or 23Jan202"), the patient had dizzy spells, more of when she is in a certain position like when she is reaching up to get something or bending down, or at night when she reclines or is switching from side to side. She stated that it usually happens when bending over, reaching up high, in a recline position or when switching sides on the pillow. She reported that she is still experiencing this symptom with no improvement and reported that dizziness worsened. In the morning of 26Jan2021, the patient reported that it was worst, the whole room was spinning but that spell went away after a few seconds. The patient reported her second dose was scheduled on 11Feb2021 and asked if the side effects after the second dose will be worse. The patient did not visit the emergency room and physician office. The outcome of the event "dizzy spells/more of when she is in a certain position like when she is reaching up to get something or bending down, or at night when she reclines or is switching from side to side" was not recovered; "the room was spinning/whole room was spinning" was recovered on 26Jan2021 (reported as "went away after a few seconds"); and "her scalp was itching and her back and stomach was itching" was recovered on 22Jan2021 (also reported as recovered on 23Jan2021). Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1056539
Sex: F
Age:
State: CA

Vax Date: 01/17/2021
Onset Date: 01/17/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: stuffy nose; like a cold but it doesn't feel the same as a cold; This is a spontaneous report from a contactable consumer(patient). A 70-year-old female patient received first dose BNT162B2 (Pfizer BioNTech Covid 19 vaccine, lot number EL3246), intramuscular at Arm Left on 17Jan2021 07:30 at the 70 years old at single dose for COVID-19 vaccination. The medical history included asthmatic. The concomitant medications were none. The patient had the first dose of the vaccine on the morning of 17Jan2021 and that afternoon on 17Jan2021 she started having a stuffy nose like a cold but it doesn't feel the same as a cold. This has been occurring for 9 days now. She called to ask if this was one of the more obscure side effects of the vaccine. The patient received the vaccination on the 17Jan2021, and in the afternoon of that day, she got a stuffy nose. She said that she did not see it as a side effect, but 9 days later she still has a stuffy nose. She said that she does not have a temperature, headache, or anything else going on. She said that she knows a stuffy nose is a side effect of Covid-19 though. The caller said that she has been reporting this on the (App Name) everyday. The patient said that the stuffy nose was the same as it had been. The patient said that she was not feeling sick, sick, just stuffed up. She did not have shortness of breath or anything like that. There was no History of all previous immunization with the Pfizer vaccine considered as suspect. The events did not require a visit to Emergency Room and Physician Office. There was no family Medical History Relevant to events. There was none Prior Vaccinations within 4 weeks. There were none relevant tests. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 1056540
Sex: F
Age:
State: OH

Vax Date: 01/22/2021
Onset Date: 01/25/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data: Test Date: 20210125; Test Name: blood pressure; Result Unstructured Data: Test Result:normal; Comments: Her took her blood pressure which was normal; Test Date: 20210125; Test Name: pulse; Result Unstructured Data: Test Result:normal; Comments: She took her pulse which was normal

Allergies:

Symptoms: pressure all in her head and all over her body; pressure all in her head and all over her body; Feeling flushed; Nausea; feel her heart beating; legs feet and hands would feel tingly; She went to bed around 1am. This went on all night off and on. She slept maybe about 3 hours total.; This is a spontaneous report from a contactable consumer (patient). A 84-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, NDC number: Unknown, Batch/lot number: EL9261, Expiry Date: 31May2021), via an unspecified route of administration in the left arm on 22Jan2021 at 0.3 mL, single for she did not got COVID. Medical history included continuing A-fib, takes medication for this everyday. Diagnosed at least 10 years ago. The patient's concomitant medications were not reported. Last night (25Jan2021) her symptoms started. She was unsure if it was from the vaccine or not but she was thinking it was, she had not had it before. Around 11 pm last night (25Jan2021) she got a pressure all in her head and all over her body. She felt flushed. She had nausea. She could feel her heart beating. She could really feel it. It was not abnormal. She did have A-fib, but this was normal, not like A-fib. Her took her blood pressure which was normal. She took her pulse which was normal. She went to bed around 1am. This went on all night off and on. She slept maybe about 3 hours total. Sometimes her legs feet and hands would feel tingly. And the flushing continue- it feels like her body was hot, but it was not hot to the touch. She had felt better this morning when she got up, but she did have one bout when she was just sitting here. She had improved overall. Caller stated she already spoke to the safety department but did not have any reference number to provide. The outcome of event 'Feeling flushed' and 'Sometimes her legs feet and hands would feel tingly' was recovered on 26Jan2021, of the other events was recovering.

Other Meds:

Current Illness: AFib (Verbatim: A-fib. Takes medication for this everyday. Diagnosed at least 10 years ago.)

ID: 1056541
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: continues vomiting; developed Migraine headache and is gotten worse ever since; This is a spontaneous report received from a contactable consumer (patient's husband). A 58-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration, on 25Jan2021, at single dose, for COVID-19 immunization. The patient medical history concomitant medications were not reported. It was reported that the patient got the COVID-19 shot in the morning of 25Jan2021 (yesterday) which developed into a migraine headache that has done nothing but gotten worse and on 26Jn2021, she had continued vomiting. The reporter asked if these were normal and how long will these last. The outcome of the events was not recovered. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1056542
Sex: F
Age:
State:

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

Lab Data: Test Name: blood pressure; Result Unstructured Data: Test Result:dropped

Allergies:

Symptoms: her blood pressure also dropped; broke out in sweat; real hot flush again; the room turned a certain color, yellow, she was pale and white, and she could tell that she was going to pass out; the room turned a certain color, yellow, she was pale and white, and she could tell that she was going to pass out; she was pale and white; This is a spontaneous report from a contactable nurse (patient's mother). A 40-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; dose 1) via an unspecified route of administration on an unspecified date "3 weeks ago" as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. Fifteen minutes after the vaccination, the patient "broke out in sweat," sat down on a table where she laid her head, and felt better after drinking "coke." Two and a half hours later, the patient felt a real hot flush again, the room turned a certain color, yellow, she was pale and white, and she could tell that she was going to pass out. The patient's blood pressure also dropped. The patient was placed in a ventilated room on an inclined chair for an hour. The patient's mother wanted to know if the patient could receive the second dose of the vaccine given her reaction to the first dose. The outcomes of broke out in sweat, hot flush, the room turned a certain color, she was pale and white, she could tell that she was going to pass out, and blood pressure also dropped were unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1056543
Sex: M
Age:
State: FL

Vax Date: 01/13/2021
Onset Date: 01/14/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: broke out with a terrible rash to his chest, groin and back with terrible itching; broke out with a terrible rash to his chest, groin and back with terrible itching; This is a spontaneous report from a contactable consumer (patient). A 91-year-old male patient received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine, Lot Number EL3246 and Expiration Date unknown) via an unspecified route of administration on 13Jan2021 at single dose for COVID-19 immunisation. The patient's medical history included heart burn. The concomitant medications were reported as omeprazole (PRILOSEC) for heart burn. Patient took the Pfizer vaccine on 13Jan2021 and 1 and a half days later (evening of 14Jan2021) he broke out with a terrible rash all over his body on his chest, groin and back with terrible itching. He reports that he went to Urgent care/clinic and was prescribed prednisone for 6 days and reports that there is still a little bit there but the rash appears much better and stopped itching. The rash, it practically eliminated the rash there are still some signs of it but at the height of it, it was very vibrant and red. Also the second day he started taking another pill, Prilosec 20 mg for heart burn and he doesn't know if the rash was caused by the vaccine or the Prilosec but his question is, is that going to deter him from taking the second dose on 03Feb2021. Patient thinks he started the Prilosec either on the 14Jan2021 or 15Jan2021 and he stopped, after 2 tablets he stopped taking it because he wasn't sure, he didn't want to aggravate anything if it was caused by the Prilosec. Now asking for guidance of if he should receive the second dose. Treatment for events was prednisone. The outcome of itching was recovered in Jan2021. The outcome of rash was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: PRILOSEC [OMEPRAZOLE]

Current Illness:

ID: 1056544
Sex: M
Age:
State:

Vax Date: 01/20/2021
Onset Date:
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: woke up with huge itchy all down from his rear end to his ankle and the back side of his leg; This is a spontaneous report from a contactable consumer reported for husband. A male patient of an unspecified age received first dose of bnt162b2 (BNT162B2), via an unspecified route of administration on 20Jan2021 16:30 at SINGLE DOSE for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. No issues for a couple of days, but then in the middle of the night at 3 a.m. husband woke up with huge itchy all down from his rear end to his ankle and the back side of his leg, itch came to the front a little bit, took some Benadryl 50 mg and itch cream, it pretty much subsided. The event outcome was recovering. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1056545
Sex: F
Age:
State:

Vax Date: 12/22/2020
Onset Date:
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: joint pain; This is a spontaneous report from a non-contactable consumer (patient). This female patient of unspecified age received the 1st dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration in the right arm on 22Dec2020 at single dose for covid-19 immunisation. Medical history and concomitant medications were unknown. The patient stated: "I am having muscle... I guess is joint pain?" The patient stated that she received her first dose of the Pfizer-BioNTech COVID-19 Vaccine on 22Dec2020 and also stated it was strange that she's experiencing those side effects on the left arm because she received the injection in the right arm. 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: 1056546
Sex: F
Age:
State: FL

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: cheeks red and burning; cheeks red and burning; upper lip swelling; This is a spontaneous report from a contactable consumer (patient). This 74-year-old female patient received the 1st dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3246) via an unspecified route of administration in the left arm on 12Jan2021 at single dose for covid-19 immunisation. Medical history included allergic to a lot of antibiotics, always get reactions to drugs. Concomitant medications were unknown. The patient previously received ciprofloxacin (CIPRO) experiencing lip swelled, levofloxacin (LEVAQUIN) experiencing lip swelled, Prednisone experiencing burning cheeks. The patient experienced that her cheeks were red and burning, and upper lip swelling slightly, all on 12Jan2021. And it lasted a little over two hours. The patient was asking if it would be safe to take Benadryl before the 2nd dose of the vaccine. Outcome of all events was recovered on 12Jan2021.

Other Meds:

Current Illness:

ID: 1056547
Sex: M
Age:
State: FL

Vax Date: 01/21/2021
Onset Date: 01/25/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: tightness of the total upper torso; muscle pain; chills; sweating; nausea; dizziness; weakness; headache; This is a spontaneous report from a contactable consumer reported for self. This 71-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 21Jan 2021 15:00 Left arm at single dose (Lot # FL7262) for covid-19 immunisation. Medical history included high blood pressure, diabetes, high cholesterol, covid prior vaccination, known allergies: Penicillin, codeine. No other vaccine in four weeks. Other medications in two weeks. He experienced tightness of the total upper torso, muscle pain, chills, sweating, nausea, dizziness and weakness, headache on 25Jan2021 03:00 AM. No covid tested post vaccination. No treatments were received. Outcome of the events was recovered in Jan2021.

Other Meds:

Current Illness:

ID: 1056548
Sex: F
Age:
State: MA

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

Lab Data:

Allergies:

Symptoms: Headache; This is a spontaneous report from a contactable consumer reported for herself. This 35-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 26Jan2021 09:15 AM Left arm at single dose (Lot # EL4237) for covid-19 immunisation. No Pregnant at the time of vaccination. Medical history was none. No Allergies to medications, food, or other products. Prior to vaccination, the patient did not diagnose with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. None other medications the patient received within 2 weeks of vaccination. Headache occurred about 1 hr after receive vaccine 26Jan2021 10:15 which was non serious, went away within 2 hours. Since the vaccination, the patient has not been tested for COVID-19. No treatments were received. Outcome of the event was recovered on 26Jan2021.

Other Meds:

Current Illness:

ID: 1056549
Sex: F
Age:
State: NY

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: anxious; chills; No appetite; metallic taste in her mouth/ had a burnt taste in her mouth; burning sensation in her whole torso; fast heart rate; This is a spontaneous report from a contactable consumer reported for self and a contactable consumer (husband). This 63-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 20Jan2021 09:00 on Arm left via Intramuscular at single dose (Lot # EL3247) for covid-19 immunisation. Medical history included allergic to penicillin when she was a kid. She said that her lips swelled up. No other products. Since receiving the vaccine, she's had a burnt taste in her mouth on 20Jan2021 and also reported that she had a burning sensation in her whole torso that lasted 2-3 mins after she received vaccine on 20Jan2021 and her heart rate was racing but resolved after a few minutes. She had a metallic taste in her mouth. It made her very anxious and she was having a fast heart rate on 20Jan2021. She got panicky because of the metallic taste. She clarified that the burning sensation she felt was a burning in her whole torso on 20Jan2021 and it was extremely hot like a chemical went into her body that was burning her guts. She said that the burning sensation only lasted 2-3 minutes and was gone. She said that she got scared and her heart was racing a little bit on 20Jan2021. Her heart racing resolved that same day after a little bit. She clarified that she has like a burnt taste in her mouth. She said that it is the roof of her mouth and her tongue that taste like this. The burnt taste is still ongoing. She said that she tried to call the physician, but has not heard back yet. She said that she had chills and no appetite that day on 20Jan2021, but it was gone by the next day 21Jan2021. Outcome of the event metallic taste in her mouth/ had a burnt taste in her mouth was not recovered. Outcome of the event burning sensation, fast heart rate was recovered on 20Jan2021. Outcome of the events chills and no appetite was recovered on 21Jan2021. Outcome of other event was unknown.

Other Meds:

Current Illness:

ID: 1056550
Sex: F
Age:
State: MA

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

Lab Data:

Allergies:

Symptoms: slight soreness in my right arm; This is a spontaneous report from a contactable consumer report for self. A 25-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247) via an unspecified route of administration at right arm on 25Jan2021 15:30 at single dose for covid-19 immunization. The patient's medical history included allergies to Amoxil, but not severely. Patient was not pregnant at the time of vaccination. Prior to vaccination, patient was not diagnosed with COVID-19. Concomitant medication within 4 weeks prior to the COVID vaccine included influenza vaccine, ethinylestradiol, levonorgestrel (KURVELO), fluoxetine hydrochloride (PROZAC). On 25Jan2021 05:00 PM, patient developed just slight soreness in right arm, but that usually happens to her when got any vaccine. No treatment received for the adverse event. Event outcome was recovering. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds: INFLUENZA VACCINE; KURVELO; PROZAC

Current Illness:

ID: 1056551
Sex: F
Age:
State: WI

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

Lab Data:

Allergies:

Symptoms: sore arm; diarrhea; bad taste in her mouth/can taste vaccine in her mouth and throat; This is a spontaneous report from a contactable consumer (patient). This 67-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot#: EL1283), via an unspecified route of administration on 26Jan2021 09:55 at single dose in the left arm for COVID-19 vaccination. Medical history and concomitant medications were none. Patient got her first injection of the COVID-19 vaccine on 26Jan2021 at 09:55AM in her left arm. Patient said that the diarrhea just started on 26Jan2021, she had tried calling earlier and had to hang up because of it, maybe because she was nervous. Patient said that she tasted the vaccine constantly, she has been experiencing a bad taste in her mouth, she couldn't stand the taste. Patient couldn't get rid of the taste. She said beforehand she was scared of anaphylactic shock, but she was having the taste in her mouth and diarrhea. She said she had the taste of the vaccine in her mouth and throat on 26Jan2021. She said that everything that she eats she is trying to get taste out of her throat. Patient has done no treatment yet for the diarrhea or the taste in her mouth. She said that her arm didn't hurt afterwards and she didn't feel the shot, and now she can't touch her arm without it hurting though she has been moving her arm a lot. She said she knew that from the flu shot, but that never hurt her, this thing was sore (sore arm) on 26Jan2021. She said she wasn't worried about that though, she just wanted to know if the taste would go away, and if it was normal. She said that there was nothing that said anything about diarrhea either, and she was not sick, she didn't feel sick, there was just the taste. Outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1056552
Sex: F
Age:
State: LA

Vax Date: 01/21/2021
Onset Date: 01/24/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: trouble breathing; This is a spontaneous report from a contactable consumer. A 80-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EL3249), by injection once to upper right arm on 21Jan2021 at single dose for prevention. The patient medical history and concomitant medications were not reported. The patient experienced trouble breathing on 24Jan2021 with outcome of unknown. She got the vaccine shot last Thursday, later clarified as COVID vaccine, and she has read over the factual sheet given after the shot, she read it once quickly, will she be ok? She has difficulty breathing, one medication, she has that too, but not more often, with this she has been having it more often, she sleeps well during the night, it is just during the day. That was a severe reaction, two days ago or so, she can breathe sometime, but it's during the day, she read one dose effects say severe reaction, and it also says. she should have been given this paperwork before the vaccine, she didn't need it, she did not have an emergency, unless the second shot will be more helpful than one shot, after 3 weeks she gets another one. It says to call vaccine provider or healthcare professional if you have any effects that bother you or do not go away, how long do you wait until it doesn't go away? Why do they give the paperwork, why don't they give it at the doctor's office office before you set up an appointment to get vaccinated? Before so you can sit down and read the paperwork, she probably would not have gotten it, it says it is only only for emergency use for 16 and over, is this still a clinical trial, that information is not provided, and that burns her behind. She got the shot and 3 days later had the difficulty breathing, so she got it last Thursday, then started Sunday, Monday, into Tuesday, and it's just not. (caller did not complete sentence). Reporter email address declined. She hasn't told her doctor yet, provider's address and email address unknown. She thinks it started on Sunday, it wasn't yesterday, she thinks it was Sunday off and on, sometimes during day she can catch her breath, it may not be this or something, which is what she wants to find out, she is concerned with the idea this should not be sent out, she would not have gotten it. Has Pfizer received many calls about this, about the paperwork? It says it has not been approved, she would never have gotten it, it says only for emergencies, she doesn't have an emergency, this should have been given before the vaccination, it is probably still under clinical trial, but they are saying on TV everyone should be vaccinated, it is either up or down, yes or no, a see saw, yes they do something, then no, it's controversial, some part of paperwork says yes. Her breathing is not worse, this says it may go away in a few days, it says if it bothers you or does not go away, how long does she wait? It says severe reaction she doesn't understand, if it goes away, it doesn't bother her health, then goes away because of the vaccine inside, ok, once she got the vaccine, she had to stay in a room for 20 minutes or so, she had to stay in a room if she had a reaction. Her vaccine card says first dose, then says the hospital, she can't really read it, they write so quick. Says 11Feb2021 is her second dose She read in there, if you have an allergic reaction to other vaccines, she said no, this was her first reaction.

Other Meds:

Current Illness:

ID: 1056553
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: diarrhea; This is a spontaneous report from a contactable consumer (patient's husband). A 66-year-old female patient (wife) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on an unspecified date at single dose for covid-19 immunisation. Medical history and concomitant medications were not provided. In the morning of 26Jan2021, four and a half hour ago (unspecified time), the patient experienced diarrhea, she used the bathroom twice thus far. The reporting consumer asked if diarrhea was also reported as a side effect of the vaccine, if they recommend for her to consult a healthcare professional (HCP) at this stage. Outcome of the event was unknown. Information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1056554
Sex: F
Age:
State: MI

Vax Date: 01/24/2021
Onset Date: 01/26/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data: Test Date: 2020; Test Name: FIBO test; Result Unstructured Data: Test Result:Positive for hydrogen FIBO

Allergies:

Symptoms: a little tenderness on the injection site; diarrhea; nausea; This is a spontaneous report from a contactable consumer. This 68-year-old female consumer reported for herself that she received the 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EL9261) at single dose on 24Jan2021 at 13:00 for COVID-19 immunisation. Relevant history included thyroid removal on 11Sep2019, and tumor removed from her appendix on May2020. Relevant family medical history was none. Concomitant Products included: Levothyroxinesince Sep2019 and Ongoing. FIBO tests in 2020 that were positive for Hydrogen FIBO. The patient experienced no symptoms by then except for a little tenderness on the injection site. On 26Jan2021, she experienced a sudden onset of diarrhea and nausea at 15:00. Treatment included Zofran. The patient stated that she did get the Vsafe contact but not today (26Jan2021). Outcome of event nausea was not resolved, outcome of other events was unknown. No emergency room required, no physician office visit. No any other vaccinations within four weeks prior to the first administration date of the suspect vaccine.

Other Meds: LEVOTHYROXINE

Current Illness:

ID: 1056555
Sex: F
Age:
State: NC

Vax Date: 01/24/2021
Onset Date: 01/24/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: headache; sweats; feverish; chills; low blood sugar symptoms; weakness; This is a spontaneous report from a contactable healthcare professional. This 66-year-old female patient received 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, lot EL3247) on 24Jan2021 at 11:15 AM at left arm for COVID-19 immunization in hospital. Historical vaccine included first dose for BNT162B2 (lot EK5730) on 02Jan2021 at 11:30 AM at left arm for COVID-19 immunization. Medical history included hypo thyroid, parox afib, high blood pressure (HBP), obesity and allergies: bupropion hydrochloride (WELLBUTRIN), soy. Concomitant drugs included metoprolol, apixaban (ELIQUIS), fluoxetine hydrochloride (PROZAC), losartan potassium (COZAAR), thyroid (ARMOUR THYROID) and more. On the day of injection on 24Jan2021 at 04:00 PM, the patient had low blood sugar symptoms, weakness, which resolved in a few hours. On second day, symptoms of low Blood sugar, sweats, feverish, chills, on third day feverish symptoms of low blood sugar, sweats, feverish, headache. No treatment was received. The outcome the events was unknown.

Other Meds: ARMOUR THYROID; COZAAR; ELIQUIS; METOPROLOL; PROZAC

Current Illness:

ID: 1056556
Sex: F
Age:
State: NY

Vax Date: 01/24/2021
Onset Date: 01/24/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data: Test Date: 20210124; Test Name: Body temperature; Result Unstructured Data: Test Result:100 Fahrenheit; Comments: about 100F

Allergies:

Symptoms: Fatigue; Headache; fever (~100F); joint pain; chills; facial rash (flat, bright red rash on both cheeks and chin); This is a spontaneous report from a contactable consumer (patient). A 32-years-old female patient (not pregnant) received 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: EL8982), via an unspecified route of administration on 24Jan2021 at 12:15 at single dose in left arm for COVID-19 immunisation. Medical history included depression and anxiety. Concomitant medication included sertraline and buspirone, both from unknown date for unknown indication. The patient experienced fatigue, headache, fever (~100f), joint pain, chills, facial rash (flat, bright red rash on both cheeks and chin), all on 24Jan2021 18:30 with outcome of recovering. No treatment was received. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, patient had not been tested for COVID-19. This case was reported as non-serious.

Other Meds: SERTRALINE; BUSPIRONE

Current Illness:

ID: 1056557
Sex: F
Age:
State:

Vax Date: 01/21/2021
Onset Date:
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: swelling/tingly on her right facial cheek; swelling/tingly on her right facial cheek; This is a spontaneous report from a contactable Other HCP (patient). This 40-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose on 21Jan2021 for COVID-19 immunisation. Medical history included rosacea. Concomitant medication was not reported. Patient received vaccine on Thursday and had been experiencing swelling/tingly on her right facial cheek. She saw both her PCP and dermatologist and has a history of rosacea. Her dermatologist told her to take cetirizine hydrochloride (ZYRTEC) for a week. Patient asked if this was a reported side effect, the efficacy after one dose; if could get second dose after having a reaction to the first vaccine; efficacy against other variants of the virus; information on rosacea/ autoimmune patients. The outcome of events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1056558
Sex: M
Age:
State: OR

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chills/shivers (first day); Mild fever (first day); Lymph node inflammation in neck (on and off since the vaccine); Headache; Arm pain at injection; This is a spontaneous report from a contactable consumer (patient). A 43-year-old male patient received the first dose of BNT162B2 (lot number: EL3247), via an unspecified route of administration in left arm on 19Jan2021 13:00 at single dose for COVID-19 immunisation. The patient medical history was not reported. Concomitant medication included cannabis. The patient experienced chills/shivers (first day), mild fever (first day), lymph node inflammation in neck (on and off since the vaccine), headache, and arm pain at injection on 19Jan2021 16:00. No treatment was received for these events. Outcome of the events was unknown.

Other Meds: CANNABIS

Current Illness:

ID: 1056559
Sex: F
Age:
State: NY

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

Lab Data: Test Date: 20210110; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: Body aches; Joint pains; Chills; Right arm injection muscular pain radiating to elbow; Slight nausea; Slight headache; Right arm injection muscular pain radiating to elbow; This is a spontaneous report from a contactable Nurse. This 51-year-old female Nurse (patient) reported for herself that she received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number=EL3246), intramuscular at right arm on 25Jan2021 15:30 at single dose for COVID-19 immunization. Facility type vaccine: Hospital. Medical history included HTN, cholesterol, known allergies: sulfa. Historical vaccine included the first dose of BNT162B2 (lot number=EJ1686) on 04Jan2021 13:00 via intramuscular at left arm for COVID-19 immunization. Concomitant medication included amlodipine, rosuvastatin calcium (CRESTOR), clonazepam. On 26Jan2021 12:00, patient had body aches, joint pains, chills, right arm injection muscular pain radiating to elbow, slight nausea, slight headache with outcome of unknown. No treatment was received. The patient underwent lab tests included COVID-19 virus test (nasal swab): negative on 10Jan2021. Patient was not pregnant. No other vaccine in four weeks. No covid prior vaccination.

Other Meds: AMLODIPINE; CRESTOR; CLONAZEPAM

Current Illness:

ID: 1056560
Sex: M
Age:
State: WV

Vax Date: 01/22/2021
Onset Date: 01/25/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: diarrhea; This is a spontaneous report from a contactable consumer (patient). A 75-year-old male patient received his 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EL9261) at single dose on 22Jan2021 about 14:40 intramuscular in right shoulder for COVID-19 vaccination. Medical history, concomitant drugs, and family medical history relevant to event were reported as "none". Patient had no history of all previous immunization with the Pfizer vaccine considered as suspect, no additional Vaccines Administered on Same Date of the Pfizer Suspect, no prior vaccinations (within 4 weeks), no relevant tests. Patient experienced diarrhea at about 8-9am 25Jan2021. Patient reported that he had had diarrhea for the last 24 hours (as of 26Jan2021). It started on 25Jan2021. Patient stated that his diarrhea did not go away. Usually he would go to the bathroom 3-4 times and it would go away, but this was not going away. No investigation assessment performed. The event did not require a visit to Emergency Room/ Physician Office. Outcome of the event was not resolved.

Other Meds:

Current Illness:

ID: 1056561
Sex: F
Age:
State: TX

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 02/26/2021
Hospital:

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

Allergies:

Symptoms: Neck/back chest pain; Neck/back chest pain; Neck/back chest pain; dizzy; weak; fever; This is a spontaneous report from a contactable nurse (the patient). This 43-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number: EL9262), dose 2, single dose via an unspecified route of administration in the left arm on 26Jan2021 at 10:00 AM (at the age of 43- years-old) for COVID-19 vaccination. The patient's medical history included hypertension, hyperlidemia, pre-cancer cells in cervix, hysterectomy and allergy to penicillin. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number: ELO1423, expiration: 1/2021), single dose, dose 1 in the right arm on 05Jan2021 at 10:00 AM. Concomitant medications included atorvastatin, hydrochlorothiazide, losartan potassium (LOSARTAN/HCTZ), fluoxetine (PROZAC) and zolpidem (AMBIEN). On 27Jan2021, the patient had neck, back and chest pain, dizzy, weak and fever. The events were reported as non-serious. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. No therapeutic measures were taken as a result of neck, back and chest pain, dizzy, weak and fever. The clinical outcome of neck, back and chest pain, dizzy, weak and fever was not recovered . The patient has been tested for COVID-19 since having the vaccine. On 25Jan2021, COVID rapid test was negative.

Other Meds: ATORVASTATIN; LOSARTAN/HCTZ; PROZAC; AMBIEN

Current Illness:

ID: 1056562
Sex: M
Age:
State: MD

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

Lab Data: Test Date: 20210118; Test Name: Antibody; Test Result: Negative

Allergies:

Symptoms: That night at 1:30 am started getting very nauseous and started vomiting. All of the next day I was extremely nauseous and unable to eat anything. I vomited up stomach acid. I have been taking Zofran; That night at 1:30 am started getting very nauseous and started vomiting. All of the next day I was extremely nauseous and unable to eat anything. I vomited up stomach acid. I have been taking Zofran; That night at 1:30 am started getting very nauseous and started vomiting. All of the next day I was extremely nauseous and unable to eat anything. I vomited up stomach acid. I have been taking Zofran; This is a spontaneous report from a contactable other healthcare professional (the patient).This 50-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number: EL9262), dose 2, single dose via an unspecified route of administration in the left arm on 25Jan2021 at 09:00 AM for COVID-19 vaccination. The patient's medical history included type 2 diabetic. The patient had no allergies to medications, food, or other products. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number: EK4176), single dose, dose 1 in the left arm on 07Jan2021 at 12:00 PM. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient received other medications within 2 weeks of vaccination. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. On 26Jan2021 at 1:30 AM, he started getting very nauseous and started vomiting. All of the next day, he was extremely nauseous and unable to eat anything. He vomited up stomach acid. He took ondansetron (ZOFRAN) for the nausea. It is now two days later and the nausea is better but still can't work or eat. The events were reported as non-serious. Therapeutic measures taken as a result of nausea included ondansetron (ZOFRAN). The clinical outcome of nauseous, vomiting and unable to eat was recovering. The patient has not been tested for COVID-19 since having the vaccine.

Other Meds:

Current Illness:

ID: 1056563
Sex: F
Age:
State: MN

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

Lab Data:

Allergies:

Symptoms: 1st dose: 24 hrs after administration, I developed a searing migraine that lasted for approx 15 hours. No medications could touch the pain and it felt like my brain and eyeballs were going to explore; 1st dose: 24 hours after administration, I developed a searing migraine that lasted for approx 15 hours. No medications could touch the pain and it felt like my brain and eyeballs were going to explor; 1st dose: 24 hours after administration, I developed a searing migraine that lasted for approx 15 hours. No medications could touch the pain and it felt like my brain and eyeballs were going to explor; This is a spontaneous report from a contactable self-reporting other health professional. A 36-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number EJ1686), intramuscularly on an unspecified date in Jan2021 at 13:00 (at the age of 36-years-old) as a single dose in the left arm for COVID-19 vaccination. Medical history included anaphylactic reactions to penicillin and pistachios. The patient was not pregnant at the time of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications were not reported. The patient did not receive any other vaccines within four weeks prior to the vaccination. The vaccine was administered to the patient in a hospital. The patient reported that twenty-four hours after administration she developed a searing migraine that lasted for approximately fifteen hours. She stated that "no medications could touch the pain" and it felt like her brain and eyeballs were going to explode. The patient specified that she did not receive any treatment for the events. The clinical outcomes of migraine, sensation of pressure and eye discomfort were reported as recovering. It was also reported that since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1056564
Sex: F
Age:
State: MI

Vax Date: 01/20/2021
Onset Date: 01/25/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: diarrhea; vomiting; This is a spontaneous report from a contactable consumer (patient). A 91-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on 20Jan2021 at 11:45 (at the age of 91-years-old) as a single dose in the left arm for COVID-19 immunization (tired of being cooped up in the house). Medical history included atrial fibrillation and patient had a pacemaker, both from an unknown date. Concomitant medications were not reported. The patient did not receive other vaccines within four weeks prior to vaccination. On 25Jan2021, at night, the patient experienced diarrhea and vomiting. The clinical outcome of the events diarrhea and vomiting was recovered on 26Jan2021 at 02:00 and she felt good. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1056565
Sex: F
Age:
State: NJ

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

Lab Data:

Allergies:

Symptoms: Left arm very sore up through left neck; Left arm very sore up through left neck; This is a spontaneous report from a contactable consumer (patient). This 53-year-old non-pregnant female patient received the first dose of BNT12B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number EL9264) via an unknown route of administration in the left arm on 26Jan2021 (at the age of 53-years-old) at 3:30 PM as a single dose for COVID-19 immunization. The patient's medical history included hypertension and penicillin allergy, both from unknown dates and unknown if ongoing. The patient's concomitant medications included hydrochlorothiazide, valsartan (DIOVAN HCT) from an unknown date for an unknown indication; amlodipine from an unknown date for an unknown indication; fish oil from an unknown date for an unknown indication; and vitamin B complex (VITAMIN B 50) from an unknown date for an unknown indication. The patient previously took levofloxacin (LEVOQUIN) on an unknown date for an unknown indication and experienced allergies; and influenza vaccine on an unknown date for an unknown indication and experienced pain. The patient had not received any other vaccines in the 4 weeks prior to the COVID vaccine. The patient reported experiencing left arm very sore up through left neck; not red just aching and pain through the first night post injection. The patient reported being still sore on day two; much more pain than flu shot previous experience. The event was reported as non-serious and did not require hospitalization. Therapeutic measures were taken as a result of the events and included treatment with ibuprofen. The clinical outcomes of left arm very sore up through left neck were recovering. It was also reported the patient was not diagnosed with COVID-19 prior to vaccination and that the patient had not been tested for COVID-19 since vaccination. No follow-up attempts are possible. No further information is expected.

Other Meds: DIOVAN HCT; AMLODIPINE; FISH OIL; VITAMIN B 50

Current Illness:

ID: 1056566
Sex: M
Age:
State: MO

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Sore arm at injection site; This is a spontaneous report from a contactable consumer (patient). A 31-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration (left arm) on 26Jan2021 09:00 (at the age of 31years) at single dose for Covid-19 immunization. The patient's medical history included Covid-19 (prior to vaccination the patient diagnosed with COVID-19). Concomitant medications included cetirizine hydrochloride (ZYRTEC) and fluticasone propionate (FLONASE); both from an unspecified date for an unspecified indication. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 27Jan2021 07:00, the patient experienced sore arm at injection site. There was no treatment received for the adverse event. The patient has not been tested for COVID-19 since the vaccination. The outcome of event was recovering. This case is non-serious. Information on the lot/batch number has been requested.

Other Meds: ZYRTEC; FLONASE

Current Illness:

ID: 1056567
Sex: F
Age:
State: MI

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

Lab Data: Test Date: 20210125; Test Name: Nasal Swab; Result Unstructured Data: Test Result: Pending

Allergies:

Symptoms: Fever; Chills; Muscle aches; Swollen PAINFUL lymph nodes left armpit; Swollen PAINFUL lymph nodes left armpit; tingling left wrist; headache; fatigue; This is a spontaneous report from a contactable nurse (patient). A 28-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: el9261) via an unspecified route of administration on the left arm on 25Jan2021 14:30 at a single dose for COVID-19 immunization. The patient medical history was not reported. Concomitant medication included drospirenone, ethinylestradiol (NIKKI) for birth control. The patient previously received first dose of BNT162B2 on 04Jan2021 for COVID-19 immunization (lot number: ej1685, left arm, 02:00 PM). On 26Jan2021 04:00 AM, the patient experienced fever, chills, Muscle aches, swollen painful lymph nodes left armpit, tingling left wrist, headache, fatigue. No treatment was received for the events. Events were reported as non-serious: did not result in death, was not life-threatening, did not cause/prolonged hospitalization, was not disabling/incapacitating and did not cause congenital anomaly/birth defect. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient was not pregnant. Post vaccination, the patient has been tested for COVID-19, nasal swab on 25Jan2021: pending result. Prior to vaccination, the patient was not diagnosed with COVID-19. Patient had no allergies to medications, food, or other products. The facility where the vaccine was administered was in a Public Health Clinic/Veterans Administration facility. Outcome of the events was not recovered.

Other Meds: NIKKI

Current Illness:

ID: 1056568
Sex: F
Age:
State: FL

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: felt a little dizzy / If she moves too quick she is light headed; Her equilibrium is off; This is a spontaneous report from a contactable consumer, the patient. A 77-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot EL9263, first dose) solution for injection intramuscular in the right arm on 26Jan2021 (at the age of 77-years-old) as a single dose for COVID-19 vaccination. There was no medical history. Concomitant medication included lisinopril for blood pressure. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. The patient felt a little dizzy if she bends down / if she moves too quick she is lightheaded and her equilibrium was off on 27Jan2021. There was no emergency room or physician office. The outcome of the events dizziness and equilibrium loss was not recovered.

Other Meds: LISINOPRIL

Current Illness:

ID: 1056569
Sex: M
Age:
State: AR

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data: Test Date: 20210122; Test Name: Heart rate; Result Unstructured Data: Test Result:his heart would beat hard /would be fast/something; Comments: 18-20 hours after receiving injection his heart would beat hard /would be fast/something like a palpitation. The constant."

Allergies:

Symptoms: 18-20 hours after receiving the injection he noticed that "his heart would beat "hard"/heart beating fast; about 18 to 20 hours later the next morning he was experiencing something like a palpitation; arm hurt that night and the next morning/sore arm of course; This is a spontaneous report from a contactable consumer (patients wife). A 76-years-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot Number: EL9261) , via an unspecified route of administration on 21Jan2021 at 14:30 (at the age of 76-years-old) in the left arm as SINGLE DOSE for covid-19 vaccination. Medical history included cardiac murmur and Type 2 Diabetic. There were no concomitant medications. On 21Jan2021 the patient experienced arm hurt that night and the next morning/sore arm, and On 22Jan2021, 18-20 hours after receiving the injection he noticed that 'his heart would beat hard' /heart beating fast/he was experiencing something like a palpitation. Report described that it is like when you get scared. This Happens 2-3 times a day and it is not constant. The patient went to his primary care physician on Friday for a 'routinely scheduled annual check up' and mentioned this to her at his appointment. His provider encouraged him to call Pfizer and report these symptoms. His doctor is going to continue to follow up with him and if the problem persists do further tests. Lab data included heart rate on 22Jan2021 18-20 hours after injection his heart would beat hard /would be fast/something like a palpitation. The clinical outcome of heart beating fast was not recovered while palpitations and arm pain were unknown.

Other Meds:

Current Illness:

ID: 1056570
Sex: F
Age:
State: TX

Vax Date: 01/20/2021
Onset Date: 01/20/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: itching and rash on her face which turned it very red; itching and rash on her face which turned it very red; itching and rash on her face which turned it very red; This is a spontaneous report from a contactable consumer (patient). An 83-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number EL9262, expiry date unknown), via an unspecified route of administration, on 20Jan2021, at a single dose for COVID-19 immunization. Medical history included ongoing allergies (She normally gets an allergy shot for mold and stuff. She had one 8 days prior to getting the vaccine. She has not gotten one since. She is due but she cannot get it until this clears up. She is unsure of the name of the allergy shot that she gets. She had all the allergy tests years ago and has been going for the last 4 years or so. For things like mold, dust, cockroaches, grass, and trees) for which receiving allergy shot, ongoing High blood pressure, ongoing Reflux, and ongoing Osteoporosis/osteopenia. Osteoporosis runs in her family, she does not have it yet but she had Osteopenia (She started young). Concomitant medications included Allergy shot (unspecified) for about 4 years for allergies, valsartan (Started about 5 or 6 years ago) orally at 160 mg, twice a day for high blood pressure, amlodipine (Started about 5 or 6 years ago), orally at 2.5 mg, once a day for High blood pressure, lansoprazole (PREVACID) (Started about 15-20 years ago) orally at 15 mg once a day for Reflux and ibandronate sodium (started about 10 years ago) via an unknown route, at 150 mg once a month for Osteoporosis/osteopenia; all were ongoing. Patient had the first shot of the vaccine last Tuesday. She stayed for half an hour and was fine. She left there and 10 minutes later while driving she started getting itchy around her face mask. She thought it was the mask irritating her skin. As the day progressed her cheeks and under her chin were getting red and itchy. She took Benadryl and the next day it got worse. She called the doctor and they put her on 20mg Prednisone two times a day. That was a week ago Tuesday. She called her allergist and he thought it was the poly glycol peg that is in the vaccine. He will test her after it is all out of her system. Both her regular doctor and her allergist told her not to take the second shot because it was too close a situation. She did not have an anaphylactic reaction, but if she had not jumped on it right away what could have happened. She is wondering if company has any data on the efficacy of the first shot if going on Prednisone right after? She started the Prednisone the next night. She is tapering off now. She still has a little bit of heat on her face and itching under the skin. So, apparently, she had an allergy to the vaccine and was told not to get the second shot. Patient clarified that she did not get the vaccine last Tuesday. She got the vaccine last Wednesday which was 20Jan2021. She said the reaction started about 40-45 minutes after receiving the dose. She has improved about 90% since starting the Prednisone. This morning her face is a little red. She is currently weaning off the Prednisone. Her face was red and it feels a little hot. She is down to 10mg twice a day. She had started the Prednisone the next day on 21Jan2021. She started the wean yesterday. This morning her face is a littler red on her cheeks. The vaccine seems to be taking a long time to get out of her system. NDC, lot, exp are unknown for the Prednisone as it is in a pharmacy vial. Her doctor told her to stop taking Benadryl as it does not stay in the system long enough. She says the Benadryl is not in a bottle, it is in a stupid little package. LOT: SMF001. EXP: May2022. Her doctor put her on Zyrtec twice a day instead. She started that on 25Jan2021. The outcome of the events was recovering.

Other Meds: VALSARTAN; AMLODIPINE; PREVACID; IBANDRONATE SODIUM

Current Illness: Allergy; Blood pressure high; Osteoporosis; Reflux gastritis

ID: 1056571
Sex: F
Age:
State: IL

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

Lab Data: Test Date: 20210126; Test Name: Body temperature; Result Unstructured Data: Test Result:101 Fahrenheit; Comments: Fever of 101

Allergies:

Symptoms: Fever of 101; body aches like the flu; headache; like the flu; This is a spontaneous report from a contactable health care professional, the patient. A 53-years-old female non-pregnant female patient (health care professional) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot Number: EK 9231), via an unspecified route of administration in the right arm on 25Jan2021 at 14:30 (at the age of 53-years-old) as a single dose, for COVID-19 vaccination. Facility where the most COVID-19 vaccine was administered was a Nursing Home/Senior Living Facility. Medical history included breast cancer on an unspecified date (Breast cancer survivor) and Covid-19 on an unspecified date (Prior to vaccination, the patient was diagnosed with COVID-19). Concomitant medication included escitalopram oxalate (LEXAPRO), tamoxifen (TAMOXIFEN). The patient had no known allergies. No other vaccines were given within 4 weeks. Since the vaccination the patient had not been tested for COVID-19. On 26Jan2021, The patient experienced fever of 101, body aches, like the flu, headache. The events were considered non serious. The patient underwent lab tests and procedures which included body temperature:101 fahrenheit (fever 101) on 26Jan2021. No treatment was given for the events. The clinical outcome of the events Fever of 101, body aches like the flu, headache was recovering.

Other Meds: LEXAPRO; TAMOXIFEN

Current Illness:

ID: 1056572
Sex: M
Age:
State: CO

Vax Date: 01/21/2021
Onset Date: 01/01/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: diarrhea; He supposed that he is dehydrated; nausea; feeling unwell; chills; This is a spontaneous report from a contactable consumer (patient). A 71-years-old male patient received the first dose BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), lot EL3246 , unspecified route of administration on 21Jan2021 13:10 (at the age of 71-years old) as a SINGLE DOSE given in left arm for COVID-19 vaccination. Medical history included ongoing vertigo, ongoing dizziness, ongoing balance problems, ongoing vision problems, ongoing stomach problems, he lost 80lbs in a year, but his weight is starting to go back up. He has had bad health for the last 3 years. He goes to the doctors all the time. In fact, he just went to the ear, nose and throat (ENT) to find out what was going on. He has had dizziness quite often, so there are days where he just don't feel good but, he thinks it has something to do with his eyes. When he feels bad, he will lay down and close his eyes, and all of his problems go away. He went to see a retina specialist because of his continuing vision problems. The ENT doctor told him he can't help him. Concomitant medications included 6 different medications. The patient experienced side effects after getting the first dose of the vaccine. He got the first dose a week ago and he said that he experienced nausea, feeling unwell, chills and diarrhea. The patient experienced nausea, feeling unwell, chills in Jan2021 and diarrhea on 26Jan2021. He had his shot a week ago tomorrow. He was up all night last night with diarrhea, he was up probably up 10 times. He was supposed to go in to get his teeth pulled today, but he just can't do it. He does have some chills and nausea. He is feeling unwell. He supposed that he is dehydrated in Jan2021. The diarrhea just started last night, 26Jan2021. He got up about 6:15 this morning and that was the last time he had diarrhea. He still has nausea, but he hasn't had any other diarrhea. He has some nausea from the time to time. He doesn't have any COVID symptoms that he can tell. He is feeling unwell, and has the nausea and chills, but he does not have any fever. He hasn't had a fever and he can still smell and taste and all of that stuff. One thing he did notice after he got his COVID-19 shot was that he did not have any symptoms of any kind. He never had pain in his arm, nothing. He received the vaccine on 21Jan2021, and he never felt a thing or anything that would associate with the shot. The consumer doesn't know if what he is going through is caused by the shot or not. Outcome of the events was unknown.

Other Meds:

Current Illness: Balance disorder; Dizziness; Stomach upset; Vertigo; Vision abnormal

ID: 1056573
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: The next day I felt intense lethargy; Soreness of the injection site; Dizzy; Light-headed/ Light headedness; Intense chills; Shaking; Feverish; Nausea; Body aches; This 25- year-old female patient contactable other HCP (reported for herself) received the second dose of COVID-19 vaccine (UNSPECIFIED TRADE NAME)(lot EL3247; expiration not provided), via an unspecified route of administration, on 25Jan2021 at 10:00 AM (at the age of 25-years-old) as a single dose for COVID-19 immunization. The facility where COVID-19 vaccine was administered was at a hospital and anatomically located on the left arm. Patient is not pregnant. The patient received the first dose of COVID-19 vaccine (UNSPECIFIED TRADE NAME)(lot EL0142; expiration not provided), via an unspecified route of administration, on 04Jan2021 at 11:00 AM (at the age of 25-years-old) as a single dose for COVID-19 immunization. Medical history included: allergies to: Azithromicin, raw fruit (apples, peaches, pears, plums, cherries, apricot). Concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 25Jan2021 at 11:00pm, she reported "Within the first 15 min I felt dizzy and light-headed, that subsided after that. Around 12hours later I had intense chills, shaking, feverish, nausea and body aches. This lasted for around 5 hours, no medication was taken to treat. The next day I felt intense lethargy and light-headedness. The day after the lethargy continued with body-aches and continued soreness of the injection site" The clinical outcome of the events dizzy, light-headed, intense chills, shaking, feverish, nausea was recovering; the outcome of the events lethargy, body-aches, continued soreness of the injection site was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1056574
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: After she got the vaccine this pain in her knee increased; sore arm; This is a spontaneous report from a contactable consumer, the patient. A female patient of an unspecified age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number unknown), via an unspecified route of administration on an unspecified date in Jan2021(at an unknown age) as a single dose for COVID-19 vaccination. Medical history was reported as arthritis, hip and knee pain which she attributed to the cold weather. The patient's historical vaccinations included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number unknown) on an unspecified date for COVID-19 immunization. Concomitant medications were not provided. The reporter stated that, on an unspecified date in Jan2021 (reported as "last Monday") she got the second dose of "the COVID shot." Prior to this she had arthritis and hip and knee pain which she attributed to the cold weather. After she got the vaccine this pain in her knee increased and she also experienced a sore arm which went away two days after. The clinical outcomes of knee pain increased was reported as unknown. The clinical outcome of sore arm was reported as resolved on an unspecified date in Jan2021.

Other Meds:

Current Illness:

ID: 1056575
Sex: F
Age:
State: NC

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

Lab Data: Test Date: 20210126; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20210126; Test Name: PCR; Test Result: Negative

Allergies:

Symptoms: intense upper stomach pains (difficult time bending over, etc); Difficult time breathing/shortness of breath; This is a spontaneous report from a contactable healthcare professional. This 27-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number EL3247) intramuscularly in the left arm on 25Jan2021 (at the age of 27-years-old) at 09:00 as a single dose for COVID-19 immunization. The patient's medical history was not reported. The patient had no known allergies. Prior to vaccination the patient was not diagnosed with COVID-19. Concomitant medication included escitalopram oxalate (LEXAPRO) from an unknown date for an unknown indication, dicyclomine from an unknown date for an unknown indication, doxycycline from an unknown date for an unknown indication, levothyroxine from an unknown date for an unknown indication, birth control from an unknown date for an unknown indication and women's multivitamins from an unknown date for an unknown indication. The patient had not received any other vaccine within 4 weeks prior to the vaccine. On 26Jan2021 at 08:00 the patient experienced intense upper stomach pains (difficult time bending over, etc.). Additionally, she experienced a difficult time breathing/shortness of breath. The patient reported the events resulted in an emergency room or urgent care visit. It was unknown if the patient received treatment for the events. The clinical outcomes of intense upper stomach pains (difficult time bending over, etc.) and a difficult time breathing/shortness of breath were recovering. It was also reported that since the vaccination the patient had tested negative for COVID-19 on 26Jan2021 via nasal swab and polymerase chain reaction tests.

Other Meds: LEXAPRO; DICYCLOMINE; DOXYCYCLINE; LEVOTHYROXINE

Current Illness:

ID: 1056576
Sex: F
Age:
State: NC

Vax Date: 01/23/2021
Onset Date:
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: sinus infection; This is a spontaneous report from a contactable consumer (patient). A 67-year-old female patient received dose 1 of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and Expiration date was unspecified) via an unspecified route of administration on 23Jan2021 (at the age of 67 years old) in a single dose for COVID-19 immunisation. No Medical history or concomitant medication reported. The patient experienced sinus infection on an unspecified date. The patient was prescribed Cefdinir 300mg, twice daily and Methylprednisolone 4mg once daily for 7days. The patient wanted to check about the medications that her doctor has given her for the sinus infection to see if it will override the effects of the COVID vaccine. Outcome of event sinus infection was unknown. The lot number for the vaccine BNT162B2 was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1056577
Sex: F
Age:
State: GA

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data: Test Date: 20210127; Test Name: Fever; Result Unstructured Data: Test Result:99.8; Comments: I felt worse and had a fever of 99.8

Allergies:

Symptoms: headache/ headachy; muscle aches; sore throat; sore arm; I felt worse; fever of 99.8; just felt overall very sick - flulike; just felt overall very sick - flulike; remaining very fatigued and slightly headachy; This is a spontaneous report from a contactable nurse (patient). This 68-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number EL8982; dose 2) intramuscularly on 26Jan2021 at 13:00 (at the age of 68-years-old) as a single dose in the left arm for COVID-19 immunization. Medical history included prolactinoma and osteoporosis. The patient was not pregnant at the time of vaccination. The patient did not receive any other vaccines within 4 weeks prior of the vaccine. The patient did not have COVID-19 prior to vaccination. Concomitant medications included vitamin D3 and bromocriptine (PARLODEL) from unknown dates for unknown indications. The patient had no known allergies. The patient previously received BNT162B2 (dose 1; lot number EL0142; left arm) on 05Jan2021 at 13:00. The patient felt fine until 26Jan2021 at 22:00- bedtime. She woke up during the night with a headache, muscle aches, sore throat, and sore arm. She tried to sleep it off but when she awoke at 07:00 she felt worse and had a fever of 99.8 and felt overall very sick- flulike. The patient was treated with ibuprofen. The patient started feeling better by about 14:00 "the next day" (unspecified) although she remained very fatigued and slightly "headachy." The clinical outcomes of headache, muscle aches, sore throat, sore arm, fever, flulike symptoms, and fatigue were recovered. It was also reported that since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are needed. No further information is expected.

Other Meds: PARLODEL; VITAMIN D3

Current Illness:

ID: 1056578
Sex: M
Age:
State: IL

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

Lab Data:

Allergies:

Symptoms: Loss of taste; right kidney pain severe; injection site pain; This is a spontaneous report from a contactable consumer (patient). This 60-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; dose 1) via an unspecified route of administration on 25Jan2021 at 10:00 (at the age of 60-years-old) as a single dose in the left arm for COVID-19 immunization. Medical history included chronic back pain, scoliosis, kidney stones, 3 double hernias, venous deficiency, fibromyalgia, 2 torn ligaments right foot, diabetes, and diabetic neuropathy. The patient did not receive any other vaccines within four weeks prior to the vaccine. The patient did not have COVID-19 prior to vaccination. The patient received unspecified concomitant medications. The patient previously took morphine from an unknown date for an unspecified indication and experienced allergy. On 25Jan2021 at 10:15 the patient experienced loss of taste, right kidney pain severe, and injection site pain. The patient was not treated for the events. The outcome of the events was not recovered. It was also reported that since the vaccination, the patient had not been tested for COVID-19. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow-up.

Other Meds:

Current Illness:

ID: 1056579
Sex: M
Age:
State: MO

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

Lab Data:

Allergies:

Symptoms: Lathargic; headache; muscle ache; chills; This is a spontaneous report from a contactable consumer (Patient). A 40-year-old male patient received first dose of BNT162B2 (COVID 19, Pfizer/BionTech, Solution for injection, Lot number: EN5318), via an unknown route administration on 26Jan2021 12:00 on left arm at single dose for Covid-19 immunization at Workplace clinic. The patient didn't received any other vaccines within 4 weeks prior to the COVID vaccine. No allergies to medications, food, or other products was reported. Concomitant medications the patient received within 2 weeks of vaccination included bupropion (buproprion), buprenorphine hydrochloride (SUBUTEX) and trazodone (trazadone). On 26Jan2021 at 18:00, the patient experienced lathargic, headache, muscle ache, chills. No treatment was received for the events. Prior to vaccination, the patient wasn't diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. Outcome of events at the time of last observation was recovering. Information regarding lot/batch number has been requested.

Other Meds: BUPROPION; SUBUTEX; TRAZODONE

Current Illness:

ID: 1056580
Sex: F
Age:
State: KS

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

Lab Data: Test Date: 20210127; Test Name: Temp; Result Unstructured Data: Test Result:lightly elevated; Test Name: Covid-19; Result Unstructured Data: Test Result:Prior to vaccination, was the patient diagnosed wi; Comments: Prior to vaccination, was the patient diagnosed with COVID-19?:Yes

Allergies:

Symptoms: got dizzy; felt queasy; Temp was lightly elevated; Sore injection site; Could not sleep, very uncomfortable.; Got hot and sweaty about 3 1/2 hours after shot.; Got hot and sweaty about 3 1/2 hours after shot.; administration_date=26Jan2021; other vaccine date = 26Jan2021; administration_date=26Jan2021; other vaccine date = 26Jan2021; This is a spontaneous report from a contactable consumer (patient). A 63-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: unknown) via an unknown route of administration on left arm (L shoulder/Arm) on 26Jan2021 at 09:00 AM at the age of 63 years old at a single dose for COVID-19 immunization. Patient was not pregnant at the time of vaccination. Medical history included RA (Rheumatoid arthritis), Penicillin allergy and covid-19 (The patient was diagnosed with COVID-19 prior to vaccination). Concomitant medications included leflunomide (ARAVA) at 20mg, once a day, daily vitamins and mesalamine 1/day. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received other medications within 2 weeks of vaccination. Also reported administration date 26Jan2021; other vaccine date 26Jan2021. On 26Jan2021 09:00, the patient experienced sore injection site (shot was given very high on L shoulder/Arm). Felt like a sharp pain when given. Got hot and sweaty about 3 and an half hours after shot. Could not sleep, very uncomfortable. Next morning (on 27Jan2021), the patient was getting ready to eat breakfast and got dizzy and felt queasy. Temp was lightly elevated. Taking Tylenol to help control soreness. The patient assessed the events as non-serious. No treatment was received in response to the adverse event. Since the vaccination, the patient hasn't been tested for COVID-19. The outcome of the events administration_date=26Jan2021; other vaccine date = 26Jan2021 was unknown and patient was recovering from all other events. Information on the lot/batch number has been requested.

Other Meds: ARAVA; DAILY VITAMINS; MESALAMINE

Current Illness:

ID: 1056581
Sex: F
Age:
State: NJ

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

Lab Data:

Allergies:

Symptoms: sore arm for two days; This is a spontaneous report received from a non-contactable consumer (patient). A 33-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, in Jan2021 (lot number and expiry date unknown), at single dose; then received the second dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on the left arm, in Jan2021 (lot number and expiry date unknown), at single dose, for covid-19 immunization, at the hospital. There were no medical history and concomitant medication. The patient has no known allergies. The patient was not pregnant at the time of vaccination. The patient did not have COVID-19 prior to vaccination and was not tested for COVID-19 post vaccination. The patient did not receive other vaccines in four weeks. The patient experienced sore arm for two days in Jan2021. Treatment included two doses of Advil. The patient recovered from the event in Jan2021. 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: 1056582
Sex: F
Age:
State: NC

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

Lab Data: Test Date: 20210126; Test Name: vital signs; Result Unstructured Data: Test Result:fine; Test Name: Weight; Result Unstructured Data: Test Result:120-123 lbs

Allergies:

Symptoms: throat tightening; discomfort; little swelling; This is a spontaneous report from a contactable consumer. An 82-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) via an unspecified route of administration on 26Jan2021 10:15 at single dose on Left arm for covid-19 immunisation. Medical history included has a lot of allergies, reactions to honey and penicillin, She experienced neck swelling after receiving penicillin. Caller took the 1st dose last 26Jan2021. she and her husband got the Covid-19 vaccine yesterday. While reporting on her husband, caller states she had a reaction to the vaccine. After receiving the shot, Caller was put on the side for half hour and 15 min later, she experienced her throat tightening on 26Jan2021. Caller was given Benadryl and observed for 10 min. Her husband received his shot but "he did not feel the needle going into his arm. Weight is between 120-123lbs. Caller mentioned that she has a lot of allergies. They watched her for 30 minutes after getting the vaccine. Within 15 minutes her throat was feeling a little tight. It cleared after about 10 minutes. Her vital signs were checked and were fine. Thy also gave her some Benadryl. She takes vitamins and minerals because she believes in them. Outcome of the event throat tightening recovered on 26Jan2021 and events was unknown.

Other Meds:

Current Illness:

ID: 1056583
Sex: F
Age:
State:

Vax Date: 01/22/2021
Onset Date: 01/22/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Hives all over from scalp to toes for over six days; This is a spontaneous report from a contactable consumer (patient). A 28-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: EL9262), via an unspecified route of administration in left arm on 22Jan2021 14:30 at a single dose for COVID-19 immunisation. Medical history included allergies to Sulfa. Patient was not pregnant at the time of vaccination. Prior to vaccination, the patient has not been diagnosed with COVID-19 Concomitant medications included bupropion hydrochloride (WELLBUTRIN) and ethinylestradiol, etonogestrel (NUVARING). The patient experienced hives all over from scalp to toes for over six days on 22Jan2021 22:30. The event was reported as non-serious. Since the vaccination, the patient has not been tested for COVID-19. No treatment was received for the adverse event. The outcome of the event was not recovered.

Other Meds: WELLBUTRIN; NUVARING

Current Illness:

ID: 1056584
Sex: M
Age:
State: MO

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

Lab Data:

Allergies:

Symptoms: Soreness at injection site in arm lasting 2 days; This is a spontaneous report from a contactable consumer (patient). A 52-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiry dates unknown), via an unspecified route of administration on left arm, on 26Jan2021 at 08:30 AM, at a single dose for COVID-19 immunization at clinic. Medical history was not reported. Patient had no allergies to medications, food, or other products. Concomitant medications included sertraline hydrochloride (ZOLOFT), atorvastatin (LIPITOR) and amlodipine besilate (NORVASC). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received other medications within 2 weeks of vaccination. On an unknown date in Jan2021 at 09:30 AM, the patient experienced soreness at injection site in arm lasting 2 days. The patient assessed the event as non-serious. No treatment was received in response to the adverse event. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, patient was not tested for COVID-19. The patient recovered from the event on an unspecified date in Jan2021. Information on the lot/batch number has been requested.

Other Meds: ZOLOFT; LIPITOR; NORVASC

Current Illness:

ID: 1056585
Sex: M
Age:
State: OH

Vax Date: 01/23/2021
Onset Date: 01/27/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data: Test Date: 20210127; Test Name: fever; Result Unstructured Data: Test Result:102 Fahrenheit; Comments: he started running a fever of 102/Caller reported he is running a fever, she had the caregiver take his temperature and it was 102 degrees Fahrenheit.

Allergies:

Symptoms: has a fever of 102; Caregiver tried to have him eat something but he took one bite said it did not taste quite right; slept most of the day/sleeping more than usual; This is a spontaneous report from a Pfizer Program. A contactable consumer reported that an 89-year-old male patient received first dose of bnt162b2 (Solution for injection) via unspecified route of administration on right arm at single dose on 23Jan2021, 14:00 (Saturday). The patient medical history included ongoing dementia (He has a little bit of dementia which has been ongoing since unknown date but at least 10 years) and Maybe some thyroid issues. The patient concomitant medication was not reported. On 27Jan2021, the patient slept most of the day/sleeping more than usual, caregiver tried to have him eat something, but he took one bite said it did not taste quite right and had a running fever of 102 degrees Fahrenheit. It was reported that patient usually wakes up around 9:00 to 9:30 and read his book but on 27Jan2021 he has been in his chair and slept most of the day, about 3-4 hours until around 14:00 to 14:30. The caregiver gave him some Tylenol and he was reading again with events ongoing and persistent. The reporter enquired whether these events were normal after vaccination because he would have had the symptoms onset closer to the date of vaccination. Therapeutic measures were taken for fever. The outcome of the events was not recovered. Information about lot/batch number has been requested.

Other Meds:

Current Illness: Dementia (He has a little bit of dementia which has been ongoing since unknown date but at least 10 years)

ID: 1056586
Sex: M
Age:
State:

Vax Date: 01/22/2021
Onset Date:
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: arm got swollen; says its "hurting like the dickens" and "can't pick up nothing."; says its "hurting like the dickens" and "can't pick up nothing."; 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 and expiration date unspecified), via an unspecified route of administration on 22Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced arm got swollen, says its "hurting like the dickens" and can't pick up nothing. Patient was asking if there was anything he can do. Outcome of events was unknown. Information on lot/batch has been requested.

Other Meds:

Current Illness:

ID: 1056587
Sex: M
Age:
State: CO

Vax Date: 01/27/2021
Onset Date: 01/27/2021
Rec V Date: 02/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Arm is very sore; This is a spontaneous report from a contactable consumer. A 77-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL9261), via an unspecified route of administration in left arm on 27Jan2021 10:00 at a single dose for COVID-19 immunisation. The patient's medical history was not reported. Prior to vaccination, the patient has not been diagnosed with COVID-19. Concomitant medications included metformin. The patient experienced arm is very sore on 27Jan2021. The event was reported as non-serious. Since the vaccination, the patient has not been tested for COVID-19. No treatment was received for the adverse event. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds: METFORMIN

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm