VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 11/12/2021
** VAERS DATABASE Last updated: November 12, 2021**
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Manufacturers

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

COVID19 Lot Number

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

Incidents per State

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

ID: 0980916
Sex: F
Age:
State: WI

Vax Date: 12/19/2020
Onset Date: 01/09/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Diarrhea; headache; chills; Extreme fatigue; This is a spontaneous report from a contactable nurse reporting for herself. A 25-year-old female patient received the 1st dose of bnt162b2 (BNT162B2, Manufacturer Pfizer-BioNTech), intramuscular in arm left, on 19Dec2020 at 12:00, at single dose, for COVID-19 immunisation. Medical history was none. Patient was not pregnant and was not pregnant at time of vaccination. Concomitant medications included cannabidiol (CBD OIL) and unspecified birth control. The patient experienced diarrhea, headache, chills and extreme fatigue all on 09Jan2021 at 16:00 with outcome of recovered in Jan2021. Extreme fatigue recovered after 36 hours. Patient did not have COVID-19 prior vaccination and was not tested for COVID-19 after vaccination. The information on the lot/batch number has been requested.

Other Meds: CBD OIL

Current Illness:

ID: 0980917
Sex: M
Age:
State: TN

Vax Date:
Onset Date: 12/24/2020
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: sinus infection; This is a spontaneous report from a contactable consumer (patient). A 66-year-old male patient received the first dose of BNT162B2 via an unspecified route of administration on 2020 at a single dose for COVID-19 immunization. There were no medical history and no concomitant medications. The patient, who worked in a hospital laboratory, stated that after the first dose, he got a sinus infection on 24Dec2020. He went through antibiotics for a week for the sinus infection which was completed by the second dose. The outcome of the event was recovered on 31Dec2020. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980918
Sex: M
Age:
State: TX

Vax Date: 12/30/2020
Onset Date: 01/01/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 20210113; Test Name: lab testing; Result Unstructured Data: Test Result:all his labs were pretty much okay

Allergies:

Symptoms: site was sore; Brain fog; Fatigue; rash on his hand; Extreme anxiety; Headache; This is a spontaneous report from a contactable consumer (patient). An adult male patient with age at vaccination of 33-years-old received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number EJ1685), via an unspecified route of administration, on 30Dec2020, at single dose for covid-19 immunization. The patient had no medical history. There were no concomitant medications. The patient stated he got the shot on 30Dec2020. There was no allergic reaction however, the site was sore, sore for a couple of days from an unspecified date. The patient added that from an unspecified date, he did have kind of brain fog, fatigue, and headache for 3 days. Those symptoms subsided after 3 days. Additionally, 2 or 3 days ago in Jan2021, he started getting a rash on his hand and have also now been suffering from extreme anxiety, fatigue and brain fog. He informed that he went to the emergency room yesterday and he was prescribed some Xanax for the anxiety and a steroid for the rash. The patient was currently taking those now. He also did some basic lab testing yesterday, 13Jan2021, and all his labs were pretty much okay. The outcome of the events site was sore, and headache was recovered on an unspecified date; the outcome of event rash on his hand was unknown; while the outcome of the other remaining events was not recovered.

Other Meds:

Current Illness:

ID: 0980919
Sex: F
Age:
State: SC

Vax Date: 12/23/2020
Onset Date:
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Name: lab work; Result Unstructured Data: Test Result:Unknown Results; Comments: I have no results yet

Allergies:

Symptoms: Bruise; Pain; Have horrific pain in back of my neck and head into my neck and not a headache; I can't turn my neck; Have horrific pain in back of my neck and head into my neck and not a headache; I can't turn my neck; wondering hurts to open my mouth and swallow; wondering hurts to open my mouth and swallow; swollen lymph nodes; This is a spontaneous report from a contactable consumer (patient). A 72-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899), intramuscular on 23Dec2020 at a single dose on upper left arm for COVID-19 immunization. Medical history included Heart stents, Lupus, Type II Diabetes, rheumatoid arthritis (Autoimmune disease), anticoagulant therapy, cardiac disorder. Concomitant medication included clopidogrel for "My heart, it's a blood thinner", carvedilol, lisinopril, and amlodipine besilate all for heart related, hydroxychloroquine sulfate (PLAQUENIL [HYDROXYCHLOROQUINE SULFATE]) for rheumatoid arthritis, rosuvastatin, semaglutide (OZEMPIC) for type II diabetes, citalopram, cyanocobalamin (VITAMIN B12 [CYANOCOBALAMIN]), moringa oleifera (MORINGA [MORINGA OLEIFERA]), and unspecified blood thinners. The patient stated, "I received the Pfizer immunization for COVID-19 on 23Dec2019 (later confirmed), and I am due to have my second dose this week and I was fine and I had just some size a small bruise. But I'm on blood thinners (further clarified and captured in medical history, hence not captured as suspect product in the tab), so I didn't think anything of it and a little pain but it went away. And then, this past Monday, which is into my third week, I have a horrific pain in the back of my neck and head into my neck and it's not a headache. It's pain and it's in the back of my head and into my neck and I can't turn my neck, right or left or up or down. It hurts to open my mouth, and it almost hurts to swallow and I am wondering if this is a reaction, so they have a delayed reaction. Is this swollen lymph nodes?" The patient stated, "I had lab work done this past Monday. I have no results yet." Therapeutic measures were taken as a result of bruise, pain, have horrific pain in back of my neck and head into my neck and not a headache; I can't turn my neck, wondering hurts to open my mouth and swallow which included ice packs and Aspirin. The outcome of the events was unknown.

Other Meds: CLOPIDOGREL; CARVEDILOL; LISINOPRIL; AMLODIPINE BESILATE; PLAQUENIL [HYDROXYCHLOROQUINE SULFATE]; ROSUVASTATIN; OZEMPIC; CITALOPRAM; VITAMIN B12 [CYANOCOBALAMIN]; MORINGA [MORINGA OLEIFERA]

Current Illness:

ID: 0980920
Sex: U
Age:
State:

Vax Date: 01/10/2021
Onset Date: 01/14/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headache; Chills; Nauseous; Not feeling well; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date were not reported), via an unspecified route of administration on 10Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced headache, chills, nauseous, and was not feeling well on 14Jan2021. The patient stated "I am curious I just had the vaccine on Sunday. It's Pfizer obviously and today I have been experiencing this side effects. Now, I had headache, chills, no fever, nauseous and just not feeling well. I missed like, I missed a week of work. Do you think I should be tested for Covid itself or it's just an allergic reaction and not worry about it?" The patient was informed about Pfizer Department. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980921
Sex: F
Age:
State:

Vax Date: 01/13/2021
Onset Date: 01/14/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Feeling weak; dizzy; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: EL3249), via an unspecified route of administration on 13Jan2021 at a single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced feeling weak and dizzy in the morning of14Jan2021. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 0980922
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Swollen lymph nodes in arm pits and they are painful; Swollen lymph nodes in arm pits and they are painful; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender 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 unspecified date at a single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. Consumer stated, "I am just calling because I have like swollen lymph nodes in my arm pits and they are like really painful. I think it's a reaction to the vaccine. I got not this on Monday but just the past, the Monday before (incomplete sentence and further not clarified) I got it, that's when I got it. I don't know if I should go see my doctor or not. It's like normal or it's like I should go see someone?". Outcome of the events was unknown. Information on the Lot/Batch Number has been requested.

Other Meds:

Current Illness:

ID: 0980923
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: Felt like revved up/Revved up, like a little hyper; This is a spontaneous report from a contactable consumer. A 71-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. Medical history included palpitations from unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient was not pregnant. The patient stated, "I did have the first injection this past Sunday. What I felt was like, I felt like I was just revved up a little bit. They had us sit for half hour and because of what I was feeling they had me to sit another 10 minutes and it pretty much passed. I did feel a little bit later that day, even up till today, just once in a while during the day. I am concerned about the second injection with that concern. And I am hearing things like we all do. I don't know what you know whether it's your drug or (other vaccine branded) that I am hearing conversation about, the second injection creating more of a reaction possibly even COVID like with fever or nausea or aching. What can I expect and is there anything I should do or be aware of with the feeling that I had of this revving up a little bit? I don't know if you, when I say revved up, like it wasn't quite palpitations because I have had that before but just revved up, I don't know how else to describe it. It didn't last very long. It just passes. Revved up, like a little hyper. I just calm myself, try to relax and calm myself." The outcome of the event was unknown. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980924
Sex: F
Age:
State: IL

Vax Date: 01/13/2021
Onset Date: 01/14/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: temp; Result Unstructured Data: Test Result:a low grade fever

Allergies:

Symptoms: Low grade fever/fever; Chills; Body ache/whole body aches; Nausea/I am getting nauseated; Not feeling well; This is a spontaneous report from a contactable nurse (patient). A 64-year-old female received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) , via an unspecified route of administration on 13Jan2021 at a single dose as patient works in a Healthcare Facility, also under the recommendation of her physician (COVID-19 immunization). Medical history included cardiomyopathy and patient has pacemaker defibrillator. Concomitant medication included sotalol. The patient had the injection (patient described the product as Pfizer EL3246) yesterday, the first dose and about 2 o'clock this morning (14Jan2021) she woke up and have been having symptoms, the side effect symptoms, she had fever, the chills, the body ache, the nausea and just not feeling well at all. The patient was still experiencing the events. The patient stated that they are actually kind of getting worse, she was getting nauseated, her entire whole body aches, not feeling well at all, she had a fever, she just took temp of herself and she has a low grade fever. No treatment was administered for the events. The outcome of the events was not recovered. Information on lot number has been requested.

Other Meds: SOTALOL

Current Illness:

ID: 0980925
Sex: F
Age:
State: TN

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

Lab Data:

Allergies:

Symptoms: Unbearable pain in her right thumb; This is a spontaneous report from a contactable pharmacist. The pharmacist reported same events for two patients. This is second report for his wife's client. A female patient of an unspecified age received her second dose BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The reporter's wife was at work (she was a hair stylist) and was talking with one of her clients. Her client (the patient) who was a nurse said recently she had also taken the vaccine (2nd shot) and said the weirdest thing had happened. She told that she can't hold anything in her right hand and she had been experiencing unbearable pain in her right thumb when she used it for anything. The reporter still spoke with the lady who had pain too and she said the same thing and they knew it came after the second shot of the vaccine. The outcome of the event was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021045702 same reporter/product/event, different patient

Other Meds:

Current Illness:

ID: 0980926
Sex: F
Age:
State: TX

Vax Date: 01/13/2021
Onset Date: 01/21/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 20210121; Test Name: Fever; Result Unstructured Data: Test Result:99.9

Allergies:

Symptoms: Fever was 99.9; Flu symptoms; Muscle aches; runny nose; diarrhea; This is a spontaneous report from a contactable consumer, the patient. This 47-year-old female patient received BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine), via an unspecified route of administration in the left arm on 13Jan2021 at 1715 (at the age of 47-years-old) as a single dose for COVID-19 vaccination. The patient's medical history included type 1 diabetes mellitus from an unknown date and unknown if ongoing and food allergy from an unknown date and unknown if ongoing (allergies: shell fish). 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. The patient was not pregnant at the time of vaccination. Concomitant medication included insulin lispro (HUMALOG), insulin glargine (BASAGLAR), cetirizine hydrochloride (ZYRTEC), montelukast sodium (SINGULAIR), gabapentin (GABAPENTIN). On 21Jan2021 at 11:00, 8 days later, the patient experienced fever was 99.9, flu symptoms, muscle aches, runny nose and diarrhea a couple times. Things tasted and smelled different or oddly before the senses going away. No therapeutic measures were taken as a result of the events. The clinical outcome of fever was 99.9, flu symptoms, muscle aches, runny nose and diarrhea a couple times was not resolved. 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: HUMALOG; BASAGLAR; ZYRTEC; SINGULAIR; GABAPENTIN

Current Illness:

ID: 0980927
Sex: F
Age:
State: GA

Vax Date: 01/11/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: I was swimming which I do every day and then when I got out of the pool was when I became dizzy and it bothered me walking; I was swimming which I do every day and then when I got out of the pool was when I became dizzy and it bothered me walking; This is a spontaneous report from a contactable consumer (patient). An 87-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL0140), via an unspecified route of administration on 11Jan2021 at 11:45 at a single dose for COVID-19 immunization. The patient's medical history included high blood pressure. Concomitant medications included metoprolol for high blood pressure and rosuvastatin calcium (CRESTOR). On 13Jan2021, the patient stated, "I was swimming which I do every day and then when I got out of the pool was when I became dizzy and it bothered me walking". The patient wanted to know if the vaccine could have been the cause. The patient did not receive any treatment for the reported events. The patient recovered from the events on 13Jan2021.

Other Meds: METOPROLOL; CRESTOR

Current Illness:

ID: 0980928
Sex: U
Age:
State:

Vax Date: 01/13/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Dizzy; Nausea; Tired; Headache; arm got a little bit tender; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), lot number: EL3302, via an unspecified route of administration on 13Jan2021 at a SINGLE DOSE for covid-19 immunization. The patient's medical history and concomitant medications were not reported. On 13Jan2021 towards the end of the day, the patient's arm got a little bit tender. It was fine, a little bit tender but nothing to worry about. But today (14Jan2021), later in the morning the patient started getting dizzy and had some nausea, was tired and had headache. The outcome of events was unknown. No follow-up attempts are possible. No further information is expected. Information on the lot/batch number has been obtained.

Other Meds:

Current Illness:

ID: 0980929
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Fatigue; Joint pain; He felt too warm; Nausea; This is a spontaneous report from a non-contactable nurse (patient). A male patient of an unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiry date not reported), via an unspecified route of administration in Jan2021 at a single dose for COVID-19 immunization. There were no medical history and concomitant medications. Patient had the first dose of COVID 19 vaccine (BNT162B2; reported as Pfizer) on an unknown date. Patient apparently received his second dose in Jan2021 (reported as looked like he got second dose on the 11th and the following days of 12th, he began experiencing symptom), he said it's been 24 hours he experienced fatigue, mild joint pain and he felt too warm, he then 4 to 8 hours he experienced nausea. No treatments were received in response to the events reported; reported as no medical treatment basically, just staying in bed. The outcome of the events fatigue, mild joint pain, he felt too warm and nausea was recovered in Jan2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0980930
Sex: F
Age:
State: IL

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

Lab Data: Test Name: blood pressure; Result Unstructured Data: Test Result:Unknown result; Test Date: 20210105; Test Name: blood work; Result Unstructured Data: Test Result:Unknown result; Test Name: temperature; Result Unstructured Data: Test Result:Unknown result; Test Name: Covid test; Result Unstructured Data: Test Result:Unknown results; Comments: Covid test pre-surgery; Test Name: Covid test; Result Unstructured Data: Test Result:Unknown results; Comments: Covid test post-surgery

Allergies:

Symptoms: Rash across face, part of her cheeks over her nose; Arm sore; Received two vaccine within 10 minutes of each other and now to be re-vaccinated again the second dose; not enough research can guarantee if that's safe; This is a spontaneous report from a contactable consumer. A 60-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: EL0140, expiry:Mar2021), intramuscular on 12Jan2021 at a SINGLE DOSE then intramuscular on 12Jan2021 at a SINGLE DOSE for covid-19 immunisation. Medical history included blood cholesterol increased, fistula, surgery on 18Dec2020. It was stated, "Sure, I am hoping you can help me. I am one of the legal guardians for our younger sister who has special needs. She is residing in a group home, group home in the city area she is currently been out of it because she has surgery. They have made arrangements for them to still ask for them to receive the first Pfizer Covid 19 Vaccination just this past Tuesday so I go from up there from my home in city and we had a problem in there they screwed up and ended up vaccinating her twice within 10 minutes. I asked the pharmacist, there I asked the RN what does that mean for her I mean I didn't know what that meant but normally we would sat for 15 minutes, they made her sat for 30 minutes. The nurse was there from the group home monitored her blood pressure and temperature and then we got in the car proceeded to drive 3 and half hour. They said just watch for temperature, labored breathing, take her to the emergency room call 911, the only thing she did have about an hour after she broke out that was "malar" (not clarified) rash across her face part of her cheeks over her nose that lasted for about 30 minutes. The next day her arm was sore which was going to happen but here is my question though she received two vaccine within 10 minutes of each other and now they are wanting her to be re-vaccinated again which would have been the second dose, supposedly on 02Feb2021. Nobody can tell me if that's safe or if that's okay, they can't guarantee, they all kept telling me, the nurse says, I called the pharmacist kept saying there's not been enough research to know if it's safe for her to get that next vaccine, so I don't know what to do." The reporter also stated, "IM, Both went for IM, first one went into her left arm and second shot was given in her right arm." The patient underwent lab tests and procedures which included blood pressure measurement: unknown result on an unspecified date, blood test: unknown result on 05Jan2021, body temperature: unknown result on an unspecified date, sars-cov-2 test: unknown results pre-surgery and post-surgery. The outcome of the event rash across face, part of her cheeks over her nose was recovered and arm sore was unknown.

Other Meds:

Current Illness:

ID: 0980931
Sex: F
Age:
State: CA

Vax Date: 12/27/2020
Onset Date: 01/01/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Rashes; I developed some lump on my neck and then my left ear; Shingles; Pain; Headache; This is a spontaneous report from a contactable nurse (patient). A 43-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot/batch number, expiration date unspecified), via an unspecified route of administration on 27Dec2020 at 16:25, at single dose for COVID-19 immunization. The patient had no medical history. The patient's concomitant medications were not reported. On 02Jan2021, the patient experienced shingles. On 06Jan2021, the patient developed some lump on neck and then on left ear. On 07Jan2021, the patient experienced rashes. The patient reported that she got her first shot 27Dec2020 and after six days she developed Shingles. She was a healthy person and then after four days, she developed some lump on her neck and then on left ear and then the next day she developed some rashes. After that, she talked to her doctor, for shingles, she gave her acyclovir medication and then she was recovering right now. According to the infection control doctor, they never heard that was the side effect. In Jan2021, the patient experienced pain and headache. Nurse stated that the primary doctor just prescribed last Friday Acyclovir, 1 gm tablet, three times a day. When she talked to her doctor, she stated that shingles was dormant, virus from the spine and when she got the vaccine, it woke up the virus from her body. It's like virus in your body, and she thought the virus reacted to this. Outcome of event shingles was recovering; and outcome of the rest of events was unknown. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0980932
Sex: F
Age:
State:

Vax Date: 01/13/2021
Onset Date:
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Name: Fever; Result Unstructured Data: Test Result:102

Allergies:

Symptoms: Fever of 102; Chills; Headache; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number/expiration date not reported), via an unspecified route of administration on 13Jan2021 15:00 at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. It was reported that the patient has actually got the COVID Vaccine on 13Jan2021 at 3 PM. The patient had fever of 102, chills and a headache on an unspecified date with outcome of unknown. Information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0980933
Sex: F
Age:
State: VA

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

Lab Data:

Allergies:

Symptoms: Numbness around my mouth and my jaws wants to lock up like headache; Numbness around my mouth and my jaws wants to lock up like headache; Numbness around my mouth and my jaws wants to lock up like headache; This is a spontaneous report from a contactable healthcare professional. A 39-year-old female patient received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine; lot number: EK4176), via an unspecified route of administration on 08Jan2021 at a single dose for covid-19 immunisation. Medical history included anxiety and some depression. Concomitant medication included sertraline hydrochloride (ZOLOFT) for anxiety and some depression, clonazepam for anxiety when it gets extreme. On an unspecified date in Jan2021, the patient experienced numbness around her mouth and her jaws wants to lock up like headache. The patient received ibuprofen, Tylenol and Advil as treatment for the event. The patient is due to receive second dose on 29Jan2021. The outcome of the events was unknown.

Other Meds: ZOLOFT; CLONAZEPAM

Current Illness:

ID: 0980934
Sex: U
Age:
State:

Vax Date: 01/13/2021
Onset Date: 01/01/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Got a large possible lump on left side of my neck and started small and then got bigger size underneath left ear; Flushed; Chills; Weird side effect; not feeling well; Got a large possible lump on left side of my neck and started small and then got bigger size underneath left ear; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number:EL3248 and expiry date unknown), via an unspecified route of administration on 13Jan2021 at a SINGLE DOSE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On Jan2021, the patient stated, "I got Covid vaccine yesterday (13Jan2021) at an Institute and I stayed for 15 minutes Since that but just about an hour ago I got a large possible lump on the left side of my neck and I was concerned because you know it started small and then it got bigger and bigger it's like the size of a "quarter" underneath my left ear (on an unspecified date) and I am just flushed and having chills and I don't know I mean it did say if have any weird side effect to call so I just wanted to make sure that it is nothing serious." The consumer stated "I am not feeling really well." The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 0980935
Sex: F
Age:
State: FL

Vax Date:
Onset Date: 01/14/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Flu like symptoms; All joints hurt/ joints were painful; Severe pain in left arm I got injection in/left arm was very painful and it was up underneath my armpit and down my arm; rash few days later and it's been itching; redness; Sunburn; Has sort of a "wound" (not clarified) on the injection "site wise"; arm is feeling itchy; This is a spontaneous report from a contactable nurse (patient). A 53-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1284 and expiry date: 30Apr2021), via an unspecified route of administration in left arm on an unspecified date at single dose for COVID-19 immunization. Medical history included haemochromatosis and GERD from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient stated, "I got the Injection, the second injection on Monday and Tuesday night I got the typical flu like symptoms. My joints were painful. I had severe pain in my left arm that I go the injection in and today like all day, my arm is feeling itchy on 14Jan2021 but I really didn't have any like redness around it but now there is like half of the side like redness on my shoulder. It feels like kind of a sunburn and has sort of a "wound" (not clarified) on the injection "site wise" (not clarified). I have been taking some Advil and I took some Benadryl the first night and I took the "Mucinex" (not clarified) (unspecified medication) it's like a "cough" medicine. The arm is getting as the days have gone on. It's just like first night the day after I got flu like symptoms, so like all of my joints hurt. The left arm was very painful and it was up underneath my armpit and down my arm and then that part improved but the left arm is now developing a rash few days later and it's been itching, like really itching." The patient considered that BNT162B2 is related to the events. The outcome of the event "pain in the left arm" was recovering while the outcome of the remaining events was unknown.

Other Meds:

Current Illness:

ID: 0980936
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Arm sore; This is a spontaneous report from a contactable nurse, the patient. A female patient of an unspecified age received the first and second doses of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Numbers: UNKNOWN); both via unspecified routes of administration on unknown dates as single doses for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On unknown dates, after both the first and second vaccinations, the patient experienced arm soreness. The patient took ibuprofen (MANUFACTURER UNKNOWN) each time for the arm soreness. The clinical outcome of the arm soreness was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 0980937
Sex: F
Age:
State: MI

Vax Date:
Onset Date: 01/11/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: I was just hot, I got hot; Hands started hurting; Really bad headache; Feeling kind of boozy; This is a spontaneous report from a contactable consumer (patient). A 44-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL3249), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history included high blood pressure and diabetic. Concomitant medications included lisinopril for high blood pressure, metformin for diabetes, and amlodipine. Today (11Jan2021), the patient just got hot and her hands started hurting. She was just feeling kind of boozy. She really had a bad headache. The patient was thinking why the lady didn't ask her if she was taking any medication or anything, she just asked if the patient was allergic to anything. The patient was not allergic to anything but she was taking medications. The patient asked if she should go and take her medication for tonight or hold until her symptoms go away. No treatment was received for the adverse events. The patient just lied down and have been sleeping for two hours. Outcome of the events was unknown.

Other Meds: LISINOPRIL; METFORMIN; AMLODIPINE

Current Illness:

ID: 0980938
Sex: U
Age:
State:

Vax Date: 01/06/2021
Onset Date: 01/16/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Nauseated; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot and expiry not reported), via an unspecified route of administration on 06Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On 16Jan2021, consumer stated, "I took the COVID vaccine on the 6th of this month and I feel real nauseated and I have been feeling this since 7 o' clock today, this evening, very nauseated and this is the second time, since I got the COVID vaccine that I have been very nauseated and it went away the first time but this time I have taken Tums and acids (Captured as Unspecified Medications), I have taken sprite, I have taken Alkasol, I still do not feel good, I feel nauseated, I can't throw up." Therapeutic measures were taken as a result of nauseated. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980939
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Received the Vaccine (Unspecified Vaccine),contracted Covid after that; Received the Vaccine (Unspecified Vaccine),contracted Covid after that; This is a spontaneous report from a non-contactable healthcare professional (patient). A patient of unspecified age and gender received first single dose of BNT162B2 (Solution for injection, batch/lot number and exp date not reported), via an unspecified route of administration on an unspecified date for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received the vaccine. Patient was a healthcare provider and then contracted Covid after that. Patient asked if she should still go ahead and still take the dose of the vaccine. The outcome of the events was unknown. No follow-up attempts are possible. Information about Lot/Batch cannot be obtained. No further information is expected; Sender's Comments: A causal association between BNT162B2 and the reported events cannot be excluded based on a compatible temporal relation. However, full immunity is only expected 2 weeks after the second dose.

Other Meds:

Current Illness:

ID: 0980940
Sex: F
Age:
State:

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Throat pain; Hard to swallow; having a hard time talking; This is a spontaneous report from a contactable consumer (patient herself). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiry date unknown), via an unspecified route of administration, on 14Jan2021 11:00, at single dose, for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient called because she received the COVID vaccine at about 11:00 this morning of 14Jan2021 and then around 16:00 this afternoon of 14Jan2021 she started getting throat pain, she found it hard to swallow and with having a hard time talking. The outcome of the events was unknown. Information about the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980941
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Legs were hurting; Everything was hurting my lower and my middle part of the body; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient stated, "It is about two things one Pneumonia Shot (Unspecified Pneumonia Shot) and then Covid-19 Shot. This first one is the Pneumonia Shot. I had the Pneumonia shot (for immunization), the second Pneumonia shot in 20Oct2020 and I had an adverse reaction to that shot." Patient then stated, "What I am concerned is about the Covid-19 Shot. I had the second one. What happened was I walked out to the doctor's office. I just started feeling that the back of my legs were hurting. I sat down in the car, everything was hurting, my lower and my middle part of the body and then I got in there to get checked with the doctor again the second time. I went in there and they checked me up and I had no blood pressure it didn't gone up and I didn't have the temperature, my bowels did not change and then they kept me in there for an hour or so to make sure that I was okay to leave and then I just left. Since this a Pfizer product the Covid 19 shot (incomplete sentence)." The outcome of the events was unknown. Information on the Lot/Batch Number has been requested.

Other Meds:

Current Illness:

ID: 0980942
Sex: F
Age:
State: FL

Vax Date: 01/14/2021
Onset Date: 01/01/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Red spot where I had the vaccine and it was itchy; Red spot where I had the vaccine and it was itchy; it still hurts and when I touch it; Pain on my arm; Rash; I do feel like a little bit of a bump; This is a spontaneous report from a contactable consumer (patient herself). A 70-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231, expiry date not reported), via an unspecified route of administration on 14Jan2021 at single dose for COVID-19 immunisation. Medical history included ongoing thyroid disorder (Verbatim: Don't have a thyroid). Concomitant medication included ongoing levothyroxine for thyroid disorder. The patient stated on 16Jan2021, "I had the COVID Vaccine on the 14th (14Jan2021). I had just pain on my arm, no side effects. But today I noticed that I had a red spot where I had the vaccine and it was itchy, so I had, but it is mild. It is nothing that's all over me, I have got a rash or anything. Just on the side it looks little red and itches and it still hurts and when I touch it, I do feel like a little bit of a bump, little bit. Is this an allergic reaction and therefore for my second dosage, will that be may not react or what?" Clinical outcome of the events was unknown.

Other Meds: LEVOTHYROXINE

Current Illness: Thyroid disorder (Verbatim: Don't have a thyroid)

ID: 0980943
Sex: U
Age:
State:

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

Lab Data: Test Name: heartbeat; Result Unstructured Data: Test Result:Rapid heartbeat

Allergies:

Symptoms: throwing up; Tiredness; Chills; Nausea; Feeling unwell; Dizzy; Rapid heartbeat; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry were not reported), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization, and gabapentin (unknown manufacturer), via an unspecified route of administration on an unspecified date at an unspecified dose and frequency for neuropathy. The patient's medical history and concomitant medications were not reported. On Monday (unknown date), the patient had the Pfizer COVID-19 Vaccine, then the patient was fine on Tuesday. On Wednesday, the patient took for the first time Gabapentin pill because the patient have neuropathy. About 2 hours after the patient took the Gabapentin, the patient started throwing up, and was not feeling well. But that all passed over. Since Wednesday (unknown date), the patient had tiredness, chills, nausea, felling unwell, dizziness, and rapid heartbeat. And the patient looked up and saw that all these could be side effects of the vaccine. The outcome of the events was unknown. Information on the batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0980944
Sex: F
Age:
State: WI

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

Lab Data:

Allergies:

Symptoms: Inflammatory pain; Little dizziness/Light headedness; Fatigue; Arthritis pain in hip, in hand and in wrist; This is a spontaneous report from a contactable nurse (patient). A 64-year-old female patient received her first dose of bnt162b2 (BNT162B2 reported as Pfizer's COVID Vaccine; lot number: EL1284; expiration date: 30Apr2021), via an unspecified route of administration left upper arm on Jan2021 at a single dose for covid-19 immunization. Medical history included lupus. There were no concomitant medications. The patient reported that she got her first dose of the COVID Vaccine 2 weeks ago today (Jan2021), and this is her second dose next Saturday. She was a non-medicated, non-kind of remission level of lupus. She mentioned that she was okay the second day, she thinks. She had a little dizziness, fatigue and light headedness that kind of thing. But the top 3 or 4 days ago, so like on her 8th or 9th day, she started to get like inflammatory symptoms like arthritis pain in her hip, in her hand, in her wrist. It was also reported that the patient experienced inflammatory pain on an unspecified date. So, she was just wondering if there are any reports of people with lupus and if the other people have reported that. She mentioned that she wanted to get the second dose but was a little concerned if those arthritis symptoms are going to be worse. No treatment was received. The causality was reported as yes. The patient she hasn't gone visit any emergency room/ physician's office for the adverse events. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 0980945
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: hiccups for last 5 days for sometimes; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiry date not reported), via an unspecified route of administration in Jan2021 at a single dose for COVID-19 immunization. The patient's medical history included patient was on hearing aid (ongoing). Concomitant medications were not reported. Patient had hiccups for the last 5 days (Jan2021), not for a while but sometimes may be every 5 or a minute. The outcome of the event hiccups was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness: Hearing aid wearer

ID: 0980946
Sex: F
Age:
State: FL

Vax Date: 01/05/2021
Onset Date: 01/01/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Name: Temperature; Result Unstructured Data: Test Result:checked 3 times, no fever

Allergies:

Symptoms: coughing; fatigued / tired; Not felt good/ Not been myself; My body has not been normal like my specimen not good and it was dark; I am very irregular with going to bathroom so I have not felt good; Might have ulcer because it burns when I eat anything; Might have ulcer because it burns when I eat anything; I have aches, body aches; Slept like all the way around the clock; This is a spontaneous report from a contactable consumer (the patient). An 83-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot E13246), via an unspecified route of administration on 05Jan2021 (at the age of 83-years old) as a SINGLE DOSE for Covid-19 immunization. Medical history included hypertension, reported as pretty regular, from an unknown date and unknown if ongoing. Family medical history included bleeding ulcer from her mother. Concomitant medications included benazepril and felodipine for hypertension. The patient experienced my body has not been normal like my specimen not good and it was dark; i am very irregular with going to bathroom so i have not felt good; might have ulcer because it burns when i eat anything; I have aches, body aches; slept like all the way around the clock all in Jan2021; I was coughing and felt fatigued / tired on 15Jan2021; and not felt good/ not been myself in Jan2021. The patient underwent lab tests and procedures which included body temperature which was checked 3 times with no fever on an unknown date. Therapeutic measures were taken as a result of slept like all the way around the clock which included ibuprofen (ADVIL). The outcome of the events bowel movement irregularity, burning sensation, ulcer, pain, hypersomnia, cough, fatigue and malaise was unknown.

Other Meds: BENAZEPRIL; FELOPINE

Current Illness:

ID: 0980947
Sex: F
Age:
State: NC

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

Lab Data:

Allergies:

Symptoms: Rash from neck all the way down, all over my body; It's been really severe; This is a spontaneous report from a contactable consumer (patient). A 56-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number: EL3249; expiration date: not known), via an unspecified route of administration in the left arm on an unspecified date at single dose for COVID-19 immunization. Medical history included thyroid (disorder). Concomitant medication included thyroid medication (unspecified). The patient experienced rash from neck all the way down, all over her body; it's been really severe on an unspecified date. The patient gone to the doctor and gave her prednisone. The patient didn't really know whether to take the second shot or not because of this. The outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 0980948
Sex: U
Age:
State:

Vax Date: 01/13/2021
Onset Date:
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Site of vaccination is red and it has a rash; Site of vaccination is red and it has a rash; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL3246), via an unspecified route of administration on 13Jan2021 at a single dose for an COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient had the COVID vaccination and had several different reactions to it. The patient stated that the one thing that was bothering the most was that the site of vaccination was red and it had a rash. The patient needed to know if there is anything to put on it to keep it from itching. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 0980949
Sex: F
Age:
State: IL

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: body ache; Chills; Low fever; Fatigue; This is a spontaneous report from a contactable consumer (patient). A 64-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: unknown (as reported: "EK5230 or EK5730, it could 52 or 57, I am not sure, that may be 5730"), via an unspecified route of administration on 14Jan2021 at single dose for Covid-19 immunization. There were no medical history and concomitant medications. The patient reported some side effects from the COVID vaccine. The patient reported she had 3 days (as reported-pending clarification) of really bad body ache, chills, low fever, and fatigue from 14Jan2021. The patient received "Flu syrup" as treatment for the adverse events. The outcome of events was not recovered (as reported "still experiencing"-pending clarification). Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980950
Sex: U
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: Had a lot of body ache; This keeps coming and going; My whole back and shoulders and arms were hurting; My whole back and shoulders and arms were hurting; My whole back and shoulders and arms were hurting; This is a spontaneous report from a contactable consumer (patient). A 80-years-old patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) , on unspecified date at SINGLE DOSE for Covid-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. Consumer stated, "I got the Pfizer vaccine last Friday, the 8 (not clarified) and I had the reaction right away that night and the side effects the whole day, I had a lot of body ache. With the week, it got somewhat better but this keeps coming and going. Like this morning, I was, also the same thing, my whole back and shoulders and arms were hurting and when I took a hot shower, it seems to help like for a half an hour or so. Now, I have the same pain again. So, I had called the center, I went back because I am in a community, and we got the vaccine there. So, I went back and I asked them, can I take Advil, because Tylenol did not do nothing for me. So, the Advil did helped me somewhat and by Saturday night, it went away. However, the whole week again comes and goes and this morning, I do not know I took Advil at night like at 01:00 and it just made me sweat but the pain in the morning, I still get the same reaction. So, what can I do for it? I am just calling to know."Outcome of the events was unknown. Information on the Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980951
Sex: U
Age:
State:

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

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

Allergies:

Symptoms: Tiredness; Headache; Muscle pain; Fever; This is a spontaneous report from a non-contactable consumer (patient). A patient of unspecified age and gender received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced tiredness, headaches, muscle pain, fever. The patient outcome of the events was unknown. No follow-up attempts are possible, information about batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0980952
Sex: U
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: I got injection site redness and it kind of hurt, just kind of pain; I got injection site redness and it kind of hurt, just kind of pain; I am kind of hard of hearing; This is a spontaneous report from a contactable consumer. A 84-years-old patient of an unspecified gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) lot number EL1283, via an unspecified route of administration on an unspecified date at SINGLE DOSE for covid-19 immunisation. The patient medical historyand concomitant medications were not reported. The patient experienced "injection site redness and it kind of hurt, just kind of pain but definitely it is red "on an unspecified date with outcome of unknown, and "I am kind of hard of hearing" on an unspecified date with outcome of unknown. The action taken was not applicable.

Other Meds:

Current Illness:

ID: 0980953
Sex: F
Age:
State: NJ

Vax Date: 12/22/2020
Onset Date: 12/22/2020
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: mild headache; This is a spontaneous report from a contactable Other Health Professional (patient). A 42-year-old female patient received 1st dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: EL0140), via an unspecified route of administration on 22Dec2020 09:00 at single dose for COVID-19 immunisation. The patient medical history was not reported. There were no concomitant medications. The patient previously took nitroglycerin and experienced drug hypersensitivity. The patient had mild headache after the first dose on 22Dec2020 with outcome of unknown.

Other Meds:

Current Illness:

ID: 0980954
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: headache; Initial information was received on 06-Jan-2021 regarding an unsolicited valid non-serious case from other health care professional. This case involves a 74-Year-old elderly male patient who experienced headache, when he received INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT]. Medical history, past medical treatment, vaccination, family history and concomitant medication were not reported. Concomitant medications were not reported. On an unknown date, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B VACCINE, suspension for injection (batch number and expiration date not reported) at an unknown dose via unknown route and unknown administration site for prophylactic vaccination. On an unknown date, the patient experienced headache, (latency: unknown) following administration of INFLUENZA QUADRIVAL A-B VACCINE. No laboratory data was reported. It was not reported if the patient received any corrective treatment for headache Outcome of the events was reported as unknown. There will be no information available regarding batch number in this case.

Other Meds:

Current Illness:

ID: 0980955
Sex: M
Age:
State: AZ

Vax Date: 10/15/2020
Onset Date: 10/15/2020
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Being miserable; Having total body aches; shaking; Feeling frigid; Initial information was received on 04-Jan-2021 regarding an unsolicited valid non-serious case from a consumer/non-hcp (healthcare professional). This case is linked to case 2021SA008600 (death case). This case involves an 85 years old male patient who became miserable (Feeling abnormal, having total body aches (pain), shaking (tremor) and feeling frigid (feeling cold), while he received vaccine INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT]. The patient's past vaccinations included Flu vaccine after which he got sick for 2 to 3 days and had a pneumonia shot a while back and had a reaction (that the provider told him the reaction was due to the immune system working and that he is sensitive to medications that with a dose of morphine he goes crazy). Medical history, medical treatments, concomitant medication and family history were not provided. On 15-Oct-2020 at 08:30 am, the patient received a 0.7 mL dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot number and expiration date were not reported) via intramuscular route in the right arm for prophylactic vaccination. On 15-Oct-2020, the patient became miserable (feeling abnormal), had total body aches (pain), shaking (tremor) and feeling frigid (feeling cold) following the administration of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE. The patient had to turn his heat up in the house due to the reaction. The patient taken 2 Advil, 2 PARACETAMOL (TYLENOL), BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE], SLEEP AID [DIPHENHYDRAMINE HYDROCHLORIDE] and kept on a cot. The patient recovered from all the events on an unknown date. There will be no information on the batch number for this case.

Other Meds:

Current Illness:

ID: 0980956
Sex: M
Age:
State: AL

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

Lab Data:

Allergies:

Symptoms: Ipol and the other vaccine, Pentacel and both have polio in the vaccine with no AE; Initial information received on 07-Jan-2021 regarding an unsolicited valid non-serious case received from other health professional. This case involves a 2 months old male patient who received a 0.5 ml dose of vaccine QUADRIVALENT INFLUENZA VACCINE [FLUZONE] (lot: UJ146AAA, expiry date: 14-Feb-2021) and POLIO VACCINE INACT 3V (VERO) (IPOL POLIO VACCINE) (lot number and expiry date unknown), both via unknown route at unknown administration site, on an unknown date (wrong product administered) as prophylactic vaccination. The patient's medical history, medical treatments, vaccinations, and family history were not provided. Concomitant vaccines included HEPATITIS B VACCINE and PNEUMOCOCCAL VACCINE 13V. It was an actual medication error due to ipol and the other vaccine, pentacel and both have polio in the vaccine (Extra dose administered). At the time of reporting, the patient had no adverse event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.

Other Meds:

Current Illness:

ID: 0980957
Sex: F
Age: 73
State: CA

Vax Date: 11/23/2020
Onset Date:
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Hives on one side of face, the side she got the vaccine; Initial information regarding an unsolicited valid non-serious case was received from a consumer (patient) via The Agency (Reference number- 00428151) and transmitted to Sanofi on 13-Jan-2021. This case involves a 73-year old female patient who experienced hives on one side of face, the side she got the vaccine (urticaria), while she received INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT]. Past medical history included allergic reaction (hypersensitivity) (she put sunscreen all over her face for a yard sale and after the yard sale she saw she had an allergic reaction). Past medical treatment(s), vaccination(s), concomitant medications and family history were not provided. At the time of the event, the patient had ongoing drug hypersensitivity (she was allergic to Sulfur and praba) On 23-Nov-2020, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [lot number: unknown and expiration date: unknown] via unknown route in an unknown administration site for prophylactic vaccination. On an unknown date, the patient experienced non serious hives on one side of face, the side she got the vaccine (urticaria), (latency: unknown) following the administration of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE. No laboratory data was reported. The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) for 9 days and EPINEPHRINE (EPIPEN) for Urticaria. On an unknown date, the patient recovered from urticaria (reported as hives lasted for 9 days). The patient wanted to know if any of the components of the vaccine contain sulfa or PABA similar to sulfur to cause this reaction and if taking Benadryl before receiving a vaccine would prevent any potential side effects. Patient stated that she was surprised that hives lasted for nine days because she read the hives would only last for three days. The patient also stated that her doctor told her the hives could not be a side effect and that she must have touched her face. There will be no information regarding batch number in this case.

Other Meds:

Current Illness: Drug allergy (she is allergic to Sulfur and praba)

ID: 0980961
Sex: U
Age:
State:

Vax Date: 11/30/2020
Onset Date:
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headache; Fever; This case was reported by a consumer and described the occurrence of headache in a adult patient who received Herpes zoster (Shingrix) for prophylaxis. On 30th November 2020 08:00, the patient received the 2nd dose of Shingrix. On an unknown date, less than a week after receiving Shingrix, the patient experienced headache and fever. On an unknown date, the outcome of the headache was unknown and the outcome of the fever was recovered/resolved. It was unknown if the reporter considered the headache and fever to be related to Shingrix. Additional information was provided as follows: The age at vaccination was not reported. The patient received the 2nd dose of Shingrix experienced fever and headache. The reporter stated that had fever for 2.5 days and have headache on and off. The reporter inquired How long do side effects like headache and fever typically would last. The information regarding consent to follow was not reported.

Other Meds:

Current Illness:

ID: 0980962
Sex: F
Age: 71
State: NY

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

Lab Data:

Allergies:

Symptoms: Some soreness of the injected arm; This case was reported by a consumer and described the occurrence of pain in arm in a 71-year-old female patient who received Herpes zoster (Shingrix) for prophylaxis. In August 2020, the patient received the 1st dose of Shingrix. On an unknown date, less than 5 months after receiving Shingrix, the patient experienced pain in arm. On an unknown date, the outcome of the pain in arm was recovered/resolved. It was unknown if the reporter considered the pain in arm to be related to Shingrix. Additional details were provided as follows: The patient had received the vaccine around August,2020 on an unknown arm and she had some soreness of the injected arm. The reporter consented to follow-up. For tolerance to the 2nd dose of Bexsero, refer case US2020248584.; Sender's Comments: US-GLAXOSMITHKLINE-US2020215496:same reporter (husband?s case) US-GLAXOSMITHKLINE-US2020AMR249184:same reporter US-GLAXOSMITHKLINE-US2020248584:same patient (2nd dose)

Other Meds:

Current Illness:

ID: 0980963
Sex: U
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: sore arm; redness; This case was reported by a physician via sales rep and described the occurrence of pain in arm in an unspecifid number of patients who received Men B NVS (Bexsero) for prophylaxis Co-suspect products included meningococcal B recom vaccine + aloh + omv pre-filled syringe device (Bexsero Pre-Filled Syringe Device) injection syringe for prophylaxis. On an unknown date, the patient received Bexsero and Bexsero Pre-Filled Syringe Device. On an unknown date, unknown after receiving Bexsero and Bexsero Pre-Filled Syringe Device, the patient experienced pain in arm and erythema. On an unknown date, the outcome of the pain in arm and erythema were unknown. It was unknown if the reporter considered the pain in arm and erythema to be related to Bexsero and Bexsero Pre-Filled Syringe Device. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional details were provided as follows: The age at vaccination was not applicable. The reporter stated that, after vaccination with Bexsero, the patient had sore arm and redness. The reporter did not consent to follow up.

Other Meds:

Current Illness:

ID: 0980964
Sex: U
Age:
State: VA

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

Lab Data:

Allergies:

Symptoms: half of the vaccine pushed out around the needle (the needle was not tight on the syringe); A spontaneous report was received from a healthcare professional concerning a patient who received Moderna's COVID-19 vaccine (mRNA-1273) and half of the vaccine pushed out around the needle (the needle was not tight on the syringe) (Incorrect dose administered). The patient's medical history was not provided. Concomitant product use was not provided. On an unknown date, the patient received their first of two planned doses of mRNA-1273 (LOT # unknown) for prophylaxis of COVID-19 infection. On an unknown date, during a drive through COVID vaccine event, after injecting the arm and pushing the plunger, about half of the vaccine pushed out around the needle (the needle was not tight on the syringe). No treatment information was provided. Action taken with the mRNA-1273 in response to the event was not reported. The event, half of the vaccine pushed out around the needle (the needle was not tight on the syringe) was considered recovered on an unknown date.; Reporter's Comments: This report refers to a case of incorrect dose administered for mRNA-1273. There were no reported adverse events associated with this case.

Other Meds:

Current Illness:

ID: 0980965
Sex: F
Age: 17
State: OK

Vax Date: 01/09/2021
Onset Date: 01/09/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: 17 years old; A spontaneous report was received from a healthcare professional concerning a 17-year-old, female patient who received Moderna's Covid-19 vaccine (mRNA-1273) and who was 17 years old (experienced inappropriate age at vaccine administration). The patient's medical history was not provided. Concomitant product use was not provided. On 09-Jan-2021 the patient received their first of two planned doses of mRNA-1273 (Lot number: 025L20A) in the left arm intramuscularly for prophylaxis of COVID-19 infection. On 09-Jan-2021 a 17-year-6-month-old female volunteered to receive the Moderna COVID-19 vaccine. Treatment information was not provided. Action taken with mRNA-1273 in response to the event was not provided. The event, inappropriate age at vaccine administration, was considered resolved on 09 Jan 2021.; Reporter's Comments: This report refers to a case of product administered to patient of inappropriate age for mRNA-1273. There were no reported adverse events associated with this case.

Other Meds:

Current Illness:

ID: 0980966
Sex: M
Age: 62
State: AZ

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Nurse did a double dose (1ml) in error; A spontaneous report was received from a nurse concerning a 62-year-old, male patient, who received Moderna's COVID-19 vaccine (mRNA-1273) and resulting in the event of inappropriate dose administered. There were no medical history and concomitant medications reported. On 06 JAN 2021, the patient received their first of two planned doses of mRNA-1273 (Batch number: 025L20A) intramuscularly for prophylaxis of COVID-19 infection. On 06 JAN 2021, the nurse gave the patient a double dose (1 ml) of the vaccine. No treatment information was provided. Action taken with mRNA-1273 in response to the event was not reported. The outcome of the event, "inappropriate dose administered" was considered resolved on 06 JAN 2021.; Reporter's Comments: This case concerns a 62-year-old, male patient who received their first of two planned doses of mRNA-1273 (Lot unknown), reporting Incorrect dose administered.

Other Meds:

Current Illness:

ID: 0980967
Sex: F
Age: 80
State: AZ

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: A nurse did a double dose (1ml) in error; A spontaneous report was received from a nurse concerning a 81-year-old, female, patient who received Moderna's COVID-19 vaccine (mRNA-1273) and a nurse did a double dose (1ml) in error. The patient's medical history was not provided. No concomitant medications were provided. On 06 Jan 2021, the patient received their first of two planned doses of mRNA-1273 (Lot Number: 025L20A) for prophylaxis of COVID-19 infection. On 06 Jan 2021, a nurse gave the patient a double dose (1 ml) of the vaccine. No treatment information was provided. Action taken with mRNA-1273 in response to the events was not reported. The outcome of the event, a nurse did a double dose (1ml) in error, was considered resolved on 06 Jan 2021.; Reporter's Comments: This report refers to a case of a 81-year-old female patient who experienced non-serious event of nurse did a double dose (1ml) in error (Inappropriate dose of vaccine administered for mRNA-1273 (lot # 025L20A, Exp date-unknown). There were no reported AEs associated with the event of Inappropriate dose of vaccine administered.

Other Meds:

Current Illness:

ID: 0980968
Sex: M
Age: 49
State: AZ

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: A nurse did a double dose (1ml) in error; A spontaneous report was received from a nurse, concerning a 49-year old male patient who received Moderna's COVID-19 vaccine (mRNA-1273) and experienced inappropriate dose administration. There were no medical history and concomitant medications reported. On 06 Jan 2020, the patient received their first of two planned doses of mRNA-1273 (Lot number: 025L20A) for prophylaxis of COVID-19 infection. On 06 Jan 2021, the patient received a double dose (1ml) of the vaccine. No treatment information was provided. Action taken with mRNA-1273 in response to the event was not reported. The outcome of the event, "inappropriate dose administered" was considered resolved on 06 Jan 2021.; Reporter's Comments: This case concerns a 49-year-old, male patient who received their first of two planned doses of mRNA-1273 (Lot Number: 025L20A), reporting Incorrect dose administered.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm