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: 1065403
Sex: F
Age:
State:

Vax Date: 01/08/2021
Onset Date:
Rec V Date: 03/02/2021
Hospital:

Lab Data: Test Name: Covid tests; Test Result: Negative ; Comments: negative 3 times

Allergies:

Symptoms: Sore throat; Pounding headache; Congested nose; Vomiting; Nausea; This is a spontaneous report from a contactable nurse (the patient). A female patient (Age: 26, Units: Unknown) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number not provided), via an unspecified route of administration on 08Jan2021 (age at vaccination unknown) as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient stated she received the second dose of the Pfizer COVID vaccine on 08Jan2021, and her fiance tested positive after 2 weeks of it. She stated she had more symptoms than him, but she tested negative 3 times when she had the COVID tests done. Her fiance tested positive on 26Jan2021. The patient's symptoms were sore throat, pounding headache, congested nose, vomiting, and nausea, on an unspecified date. The patient wanted to know if the vaccine was preventing it to show positive and if this could be a false negative. The clinical outcome of sore throat, pounding headache, congested nose, vomiting, and nausea was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1065404
Sex: F
Age:
State: FL

Vax Date: 01/28/2021
Onset Date: 01/29/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Swollen lymph node left arm; This is a spontaneous report from a contactable Other Health Care Professional, the patient. A 47-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number El3264), intramuscularly on 28Jan2021 at 15:45 (at the age of 47-years-old) as a single dose in the left arm for COVID-19 vaccination. Medical history included asthma from an unknown date and unknown if ongoing. The patient's historical vaccinations included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number El1284), on 07Jan2021at 16:40 in the left arm for COVID-19 immunization. The paktient has unspecified allergies to Penicillin. The patient previously too clindamycin (UNKNOWN MANUFACTURER) and experienced an unspecified allergy.The patient was not pregnant at the time of vaccination. Prior to the vaccination, the patient had not been diagnosed with COVID-19. Concomitant medications were not provided. On 28Jan2021 at 19:15, the patient experienced a swollen lymph node in the left arm. The patient did not receive any treatment for the event. The clinical outcome of swollen lymph node was reported as not recovered. It was also reported that since the vaccination, the patient had not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1065405
Sex: F
Age:
State: TX

Vax Date: 01/28/2021
Onset Date: 01/28/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: dizziness.; migraine; arm swollen; My finger on my left side is numb and it has a little bit of purple on the center of it; My legs were hurting like really heavy; I have not gone back to sleep and I feel like a bus hit me.; chills; the body ache; legs hurt really bad; fever; symptoms associated with the flu for a few days; feeling like really bad headache; nauseated; not feel so good; This is a spontaneous report from a contactable nurse. A 50-year-old female patient received her second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9265, expiration date: unknown), via an unspecified route of administration from 28Jan2021 to 28Jan2021 at SINGLE DOSE for COVID-19 immunization. Medical history included blood pressure. Concomitant medication included verapamil for blood pressure. The patient received her first dose of BNT162B2 on 08Jan2021 and experienced arms a little sore. On 28Jan2021 at 18:00, the patient started feeling like really bad headache and then really nauseated. The patient took medicine and took Tylenol before went in to take her shot and started getting a headache again and not feel so good. On 29Jan2021 at 02:00, the patient stated that her legs were hurting like really heavy and had not been back to sleep since 2 o clock in the morning and she felt like a bus hit her. On 29Jan2021 at 11:00, the patient stated that her finger on the left side was numb and it has a little bit of purple on the center of it. On 29Jan2021, the patient experienced chills, body ache, her legs hurt really bad, fever, symptoms associated with the flu for a few days. On 30Jan2021, the patient experienced arm swollen. On 01Feb2021, the patient experienced dizziness and migraine. The patient already took Tylenol and ibuprofen. The outcome of the event chills, fever, flu symptoms, arm swollen was recovered on an unspecified date and the outcome of the other events was unknown.

Other Meds: VERAPAMIL

Current Illness:

ID: 1065406
Sex: F
Age:
State: FL

Vax Date: 01/08/2021
Onset Date:
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fever; This is a spontaneous report from a contactable consumer. A 78-year-old female patient received her first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL3286), via an unspecified route of administration on 08Jan2021 at a single dose for COVID-19 immunization. The patient medical history was not reported. Concomitant medication included clonidine, losartan and propranolol. It was reported that the patient called after the first shot also which was on the 8th. She called on 9th because she got a fever and I asked if she can take a medication because she is trying to figure out if it is same thing interacting with anything. The outcome of the event was unknown.

Other Meds: CLONIDINE; LOSARTAN; PROPRANOLOL

Current Illness:

ID: 1065407
Sex: M
Age:
State:

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

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

Allergies:

Symptoms: positive COVID-19 test with symptoms; positive COVID-19 test with symptoms; This is a spontaneous report from a contactable consumer who reported for her husband via a Pfizer Sponsored Program, Pfizer First Connect. A male patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection) via an unspecified route of administration on an unspecified date as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The reporter stated that "her husband received the first shot and tested positive for COVID-19. Her husband had fever, colds and sore throat." The reporter wanted to know if her husband could still receive the 2nd dose of the vaccine. The clinical outcome of the event "positive COVID-19 test with symptoms" was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.; Sender's Comments: Based on the current available information and the plausible drug-event temporal association, a possible contributory role of the suspect product BNT162B2 to the development of events Drug ineffective and COVID-19 cannot be totally excluded. The case will be reassessed if additional information becomes available.

Other Meds:

Current Illness:

ID: 1065408
Sex: F
Age:
State: FL

Vax Date: 01/29/2021
Onset Date: 01/01/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data: Test Date: 20210129; Test Name: blood pressure; Result Unstructured Data: Test Result:gone up; Test Date: 202101; Test Name: Fever; Result Unstructured Data: Test Result:99; Comments: maybe 99

Allergies:

Symptoms: shot started to hurt; blood pressure was gone up; Fever; my head feels like it is going to explode; This is a spontaneous report from a contactable consumer (patient). A 79-year-old female patient received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN5318) solution for injection, via an unspecified route of administration on 29Jan2021 at 08:30 at single dose for COVID-19 immunization. The patient has a lot of medical conditions (unspecified). Concomitant medications included unspecified medications. The patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 08Jan2021 (lot number: EL3286) at single dose for COVID-19 immunization and experienced fever. The patient reported that she had her shot this morning (29Jan2021) at about 08:30 and towards evening, the shot started to hurt and so she wanted to make sure that it didn't go against anything, and put a little ice on it or maybe it was worthless on ice on certain situations after the fact that she thought this was too late. She wanted to make sure she could do that. The patient's blood pressure also went up on 29Jan2021. She was taking several different medicines for blood pressure. She took them already tonight. She was hoping that she will be feeling a little bit better. Sometimes, she gets a little fever on Jan2021, also like maybe 99 (unspecified). She just wanted to know if any of the medications were good or not for the shot. The patient was asking whether the drugs interacted. The patient also reported that when she took her first shot, she had a little fever and asked what she could take for it. An agent stated that she could take paracetamol (TYLENOL). The patient mentioned that she took her pills, otherwise, her head felt like it was going to explode on Jan2021. She took her high blood pressure medicines. She has three medications namely clonidine, losartan and propranolol. She has a lot of medical conditions that was why she was calling because she takes other medications. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1065409
Sex: U
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: Skin allergic reaction at the site of pfizer covid 19 vaccine injection; This is a spontaneous report from a contactable physician received via a Pfizer sales representative. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number and expiration date unknown), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced skin allergic reaction at the site of Pfizer COVID 19 vaccine injection on an unspecified date. The outcome of the event was unknown. No follow-up attempts are possible; information about Lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1065410
Sex: F
Age:
State: NC

Vax Date: 01/12/2021
Onset Date: 01/12/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Severe allergic reaction; wheezing; felt right through her chest like through her right side kind of going into her left; it was weird like she could feel going into her body/ suddenly felt strange sensation in her chest; heart started beating really fast/ heart started beating very rapidly; face was all red/ face growing red and swelling slightly; face was all red/ face growing red and swelling slightly; breathing was becoming labored; This is a spontaneous report from a contactable consumer (patient herself). A 75-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number: EL3248, NDC/UPC number and expiry date were unknown), via an unspecified route of administration in the right arm on 12Jan2021 at 10:00 AM at a single dose for COVID-19 immunization. The vaccine facility type was reported as the "doctor's office/urgent care." Relevant medical history included high blood pressure, but it was controlled blood pressure/hypertension; asthma, for which she was not taking medication at the time of the report, because it was under control; non allergic rhinitis; pre diabetes; and a little overweight. The patient further stated that she had just general medical history, which she had everything under control. Concomitant medications included lisinopril, montelukast sodium (SINGULAIR), atorvastatin (LIPITOR), acetylsalicylic acid (BABY ASPIRIN), and metformin. The patient previously took to iodine, doxycycline, erythromycin, and azithromycin, for which the patient had known allergies to all of it. The patient was not pregnant at the time of vaccination. The patient had no other vaccine in four weeks. The patient had no COVID-19 prior vaccination. She was not tested for COVID-19 post vaccination. The patient stated that on 12Jan2021 at 10:30, she had adverse reactions to the Pfizer vaccine; she had severe allergic reaction within about 30 minutes and then they call the paramedic she ended up and they gave her a shot, which she did not know if it was prednisone. It was further reported that she took her inhaler too as they said she was wheezing, which she didn't really feel in her lungs. The patient just felt that what happen was she went to the car as they said to wait 15 minutes as written, and she always follow the rules and the whole thing they said, she waited 30 minutes, so she went down side of her car then she figured that she could just drive off drive home. So, she was in car sitting or waiting for the last 30 minutes and all of a sudden she felt right through her chest like through her right side kind of going into her left; it was weird like she could feel going into her body, then suddenly her heart start beating really fast, and then she pulled down the vizor and looked in the rearview mirror and her face was all red, so she go back to the site. That's how she transpired and then, that's how the reaction was. It was further reported that the patient waited 15 minutes in the office, then went to car to wait additional 15 minutes, and suddenly felt strange sensation in her chest and her heart started beating very rapidly. She pulled down the visor in car and saw her face growing red and swelling slightly and her breathing was becoming labored. She had read on side effects on information she was given on departure stating symptoms of an allergic reaction. She returned to the facility at which time she was treated. The adverse events (AE) resulted in a doctor or other healthcare professional office/clinic visit. The patient had no investigation assessment. Therapeutic measures were taken as a result of all the events, which included that the patient was given a shot of 125 mg of methylprednisolone sodium succinate (SOLU-MEDROL), but another report said they gave her prednisone so they were kind of conflicting in the report, but it was a shot, and also cetirizine (ZYRTEC) and famotidine (PEPCID), and her inhaler for wheezing. The patient recovered from all the events on an unspecified date.

Other Meds: LISINOPRIL; SINGULAIR; LIPITOR [ATORVASTATIN]; BABY ASPIRIN; METFORMIN

Current Illness:

ID: 1065411
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: headache; This is a spontaneous report from a contactable consumer (the patient). A female patient (Age: 65, Units: Unknown) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number not provided), via an unspecified route of administration on 08Jan2021 (age at vaccination unknown) as a single dose for COVID-19 immunization. The patient's medical history included reactions to 'every vaccine' (unspecified). Concomitant medications were not reported. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number not provided), via an unspecified route of administration on an unspecified date (age at vaccination unknown) as a single dose for COVID-19 immunization. Prior to receiving the first dose of Pfizer COVID-19 vaccine, the patient took ibuprofen (ADVIL) 600 mg. After the first dose, she took Advil again. In the second dose of the vaccine, initially she didn't take Advil, but 2 days after the second dose, she took Advil again. The patient wanted to know if that would affect the effect of the vaccine, since she confirmed that she was having this headache in any vaccine. The patient asked if she can use antipyretics before or after vaccination with the Pfizer-BioNTech COVID-19 vaccine. She received her first Pfizer COVID vaccine; however, due to a history of reactions to 'every vaccine', she took 600 mg of Advil prior to her appointment. After her second dose, she took Advil for 2 days after due to her headache. The patient wanted to know how long after taking the COVID vaccine does Pfizer recommend taking the antibodies test, and if it was possible for her doctor to recommend a third dose of the COVID vaccine. The clinical outcome of headache was unknown. Information about Lot/Batch has been requested.

Other Meds:

Current Illness:

ID: 1065412
Sex: F
Age:
State: GA

Vax Date: 01/29/2021
Onset Date:
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: experiencing upper leg pain (flu); This is a spontaneous report from a contactable consumer (patient) from a Pfizer Sponsored Program. A female patient of unknown age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unknown route of administration on 29Jan2021 as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously received dose 1 of BNT162B2 on an unknown date. The patient experienced upper leg pain (flu) on an unknown date. The clinical outcome of the event upper leg pain was unknown. The batch/lot numbers for the vaccine, PFIZER-BIONTECH COVID-19 MRNA VACCINE, were not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1065413
Sex: F
Age:
State: TX

Vax Date: 01/27/2021
Onset Date: 01/27/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: she took a Tylenol 1 hour before her covid vaccine; This is a spontaneous report from a contactable consumer via the Pfizer Sponsored Program. A 67-year old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: UNKNOWN), via an unspecified route of administration on 27Jan2021 as a single dose for COVID-19 immunization. Medical history included ear infection. The patient's concomitant medications were not reported. The patient reported that she got the COVID-19 vaccine on Wednesday 27Jan2021. The Prior Sunday she developed inner ear infection, so she took Tylenol about an hour before the vaccine. She heard taking a pain reliever could lessen effectiveness if taken before shot. She took Tylenol about an hour before the vaccine, she inquired if that is okay. The clinical outcome was unknown. Information about Lot number has been requested.

Other Meds:

Current Illness:

ID: 1065414
Sex: F
Age:
State: GA

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

Lab Data:

Allergies:

Symptoms: she will take medication for her Sinus/she is having some sinus problems; This is a spontaneous report from a Pfizer-sponsored program. A 72-year old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) (at the age of 72-years-old), via an unspecified route of administration on an unspecified date as a single dose for covid-19 immunization. Medical history included sinus problems "this time of year and takes Mucinex DM for it." Concomitant medications were not reported. On an unspecified date, she experienced some sinus problems. The clinical outcome of the event sinus problems was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 1065415
Sex: F
Age:
State: CA

Vax Date: 12/30/2020
Onset Date: 01/01/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: suspected COVID-19 with symptoms; This is a spontaneous report from a contactable consumer (patient) via a Pfizer-Sponsored Program, Pfizer First Connect. A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection) via an unspecified route of administration on 30Dec2020 as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The reporter stated that "on 01Jan2021 she had COVID like symptoms. Her husband got COVID-19. She had not received her second dose because she was sick. Her second dose was supposed to be on 20Jan2021. She was scheduled to go back to work on 01Feb2021 and would be able to get a dose on 02Feb2021." The patient wondered if she was supposed to start over or if she could just get the second dose. The clinical outcome of the event "suspected COVID-19 with symptoms" was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1065416
Sex: F
Age:
State: LA

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

Lab Data: Test Name: SARS-CoV-2 test; Test Result: Positive

Allergies:

Symptoms: her mom tested positive with Covid-19 vaccine; COVID-19 confirmed by postiive COVID-19 test; This is a spontaneous report from a contactable consumer from a Pfizer-sponsored program, Pfizer First Connect. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on an unknown date as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient experienced a positive COVID-19 test on an unknown date. The clinical outcome of the event COVID-19 was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1065417
Sex: F
Age:
State: FL

Vax Date: 01/22/2021
Onset Date: 01/01/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data: Test Name: body temperature; Result Unstructured Data: Test Result:normal

Allergies:

Symptoms: Lethargic; Flu like symptoms; Lower part of my leg, I have little bit rash, a redness; Lower part of my leg, I have little bit rash, a redness; I have few spots on my right forearm; This is a spontaneous report from a contactable consumer. A 75-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 at the age of 75 years, on 22Jan2021 at a SINGLE DOSE for covid-19 immunisation. Medical history included atrial fibrillation from an unknown date and unknown if ongoing and anticoagulant therapy from an unknown date and unknown if ongoing. Concomitant medication included dronedarone hydrochloride (MULTAQ) at 400mg, twice daily and apixaban (ELIQUIS) at 5mg, two times daily. The patient stated, "Both my husband and I took the Covid the first shot on 22Jan2021 which was week ago today. I noticed about 4 days later (Jan2021) like I started feeling you know flu like symptoms but they were mild, if I took two an Extra strength Tylenol it went away. You know what I mean. So that one for about may be one, two may three days and that was it. I was very lethargic. The only thing I did notice that on both my legs from the ankles of about midways I have you know my leg, the lower part of my leg, I have little bit rash, a redness. It does not itch, it was not hard to the touch. My body temperature was normal. It was little red or pinkish to a little bit of red. Now, I noticed tonight that I have few spots on my right forearm. Like I said we have shot on 22nd, everything was fine, no immediate reaction or anything else and everything is okay. I just you know I feel fine but is this normal?" The patient stated, "No, they are healthy and safe about 20-25 minutes. Everything was fine and then let us go and I said couple of days later it hasn't progressed, it is very, it is on both of my lower legs from ankles midway up my legs and I noticed couple of spots on my left forearm but it hasn't gotten any worst and it hasn't gotten spread on any place other than right forearm." The patient also stated, "You mean the rash or any other the symptoms. We have the shot Friday, Saturday, Sunday, Monday. I was say this past Tuesday, around 26th (further not clarified)." The patient stated, "It was there on my legs. It hasn't moved. It hasn't gotten any worse and it is only on front it is not back on my legs. The only thing I noticed tonight that it is couple of spots on my right forearm." The consumer stated, "No, I went to see my doctor the other day for her to take look at it. I went to see PA at my doctor's office, I saw her and she said if it doesn't get worse it would probably go away." The patient also stated, "The only thing that I had done right before the Covid Vaccine. I had injection in my knee of amniotic fluid for a torn meniscus but that should not affect it." The patient underwent lab tests and procedures which included body temperature: normal on an unspecified date. The outcome of the events was unknown. Information on the Lot/Batch number has been requested.

Other Meds: MULTAQ; ELIQUIS

Current Illness:

ID: 1065418
Sex: F
Age:
State:

Vax Date: 01/21/2021
Onset Date: 01/21/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: significant lymph node swelling; body aches; unable to walk/stand; unable to walk/stand; chills; headache; sore throat; This is a spontaneous report from a non-contactable nurse. A 28-year-old female received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiration date were not reported), via an unspecified route of administration on the left arm on 21Jan2021 at single dose for COVID-19 immunisation. Medical history included asthma, fibromyalgia, anxiety, depression and known allergies: penicillin. Concomitant medication included escitalopram oxalate (LEXAPRO), loratadine (CLARITIN [LORATADINE]), fluticasone propionate (FLONASE [FLUTICASONE PROPIONATE]) and fluticasone furoate, vilanterol trifenatate (BREO ELLIPTA). The patient previously took first dose of BNT162B2 on 02Jan2021 on the left arm. The patient experienced significant lymph node swelling, body aches, unable to walk/stand, chills, headache, sore throat on 21Jan2021.The patient received no treatment. The outcome of the events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: LEXAPRO; CLARITIN [LORATADINE]; FLONASE [FLUTICASONE PROPIONATE]; BREO ELLIPTA

Current Illness:

ID: 1065419
Sex: F
Age:
State: NC

Vax Date: 01/29/2021
Onset Date: 01/29/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: My face is swelled; This is a spontaneous report from a contactable consumer (patient). An 84-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot and expiry were not reported), via an unspecified route of administration (at the age of 84years) on 29Jan2021 at 09:00 at single dose for covid-19 immunisation and diphenhydramine hydrochloride (BENADRYL), via an unspecified route of administration from an unspecified date at unspecified dose and frequency for an unspecified indication. Medical history included have a pacemaker. Concomitant medications were unspecified as stated, "I am taking lot of medication." The patient reported, "My face is swelled" on 29Jan2021. Consumer stated, "I got the Pfizer vaccine today and I looked in a mirror a couples of hours ago and my face is swelled. So, my question is should I take diphenhydramine hydrochloride or not? It got a little better but it is still swollen. I wonder if I took diphenhydramine hydrochloride would that be helpful. I am getting better." There was no treatment for the event. The action taken in response to the event for diphenhydramine hydrochloride was unknown. The outcome of the event was recovering. Information on the lot/batch number has been requested.

Other Meds: BENADRYL

Current Illness:

ID: 1065420
Sex: M
Age:
State: WI

Vax Date: 01/28/2021
Onset Date: 01/28/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: pain at the injection site; This is a spontaneous report from a contactable consumer. A 71-year-old male patient received his first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number FF09262), via an unspecified route of administration on 28Jan2021 12:00 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that the patient had pain at the injection site with the Covid-19 vaccine. It has been over 21 hours. Is due for the second one on 18Feb2021. The outcome of the event was not recovered.

Other Meds:

Current Illness:

ID: 1065421
Sex: M
Age:
State: CA

Vax Date: 02/08/2021
Onset Date:
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Coughing and nasal symptoms are listed as possible signs of Covid19 infection; reporting body aches; fever; watery eyes; sneezing; dry cough; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID19 VACCINE), via an unspecified route of administration on 08Feb2021 at SINGLE DOSE for COVID-19 immunization. The patient's medical history included Exposure to SARS-CoV-2 (around an elderly co-worker that tested positive for Covid19 infection). Concomitant medications were not reported. The patient experienced body aches (not 'itch' as reported), fever, watery eyes, sneezing, and a dry cough. Caller wanted to know if these symptoms are normal? Coughing and nasal symptoms were listed as possible signs of covid19 infection. The patient had been around an elderly co-worker that tested positive for Covid19 infection, caller did not find out until after receiving his first dose. He spent 4 - 5 hours with him, before getting his shot. If he tests positive for Covid19 infection, how does that affect his next dose which was scheduled for 01Mar2021? The outcome of the events was unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1065422
Sex: F
Age:
State: SC

Vax Date: 01/28/2021
Onset Date: 01/01/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: fever; Result Unstructured Data: Test Result:101.4; Test Date: 202101; Test Name: fever; Result Unstructured Data: Test Result:101.8; Comments: it never went over 101.8; Test Date: 20210130; Test Name: fever; Result Unstructured Data: Test Result:99; Comments: I still have just a 99 temperature

Allergies:

Symptoms: Not feeling very energetic; I did not feel good; Chills; Fever; Headache; Did not feel like eating much; Achy; This 72- year-old female patient contactable consumer (reported for herself) received the BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) (lot EL9265; expiration not provided), via an unspecified route of administration, on 28Jan2021 at 09:15 AM (at the age of 72-years-old) as a single dose for COVID-19 immunization. The facility where COVID-19 vaccine was administered was at a hospital. Medical history included: COVID in Mar2020 and was hospitalized for 10 days, hypertension, thyroid disorder, and flu shot. Concomitant medication included: Hydrochlorothiazide 12.5 mg, once a day for blood pressure and medication for thyroid reported as: "NP" 0.5gms. On 28Jan2021 later on after vaccine, she reported 9:15 pm that she did not feel good. She had chills, fever, headache, did not feel like eating much, was achy, and not feeling very energetic. During the night temperature was 101.4. At 8 in the morning, I started taking 2 Tylenol, 500 mg and it went lower but then it would come back up, so I take more. So, it never went over 101.8. now here we are on the Saturday morning and I am not feeling very energetic and I still have just a 99 temperature. Treatment included: Tylenol. The clinical outcome of the events I did not feel good, chills, fever, headache, did not feel like eating much, Not feeling very energetic, and Achy were unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: HYDROCHLOROTHIAZIDE; NP THYROID

Current Illness:

ID: 1065423
Sex: M
Age:
State: IL

Vax Date: 01/23/2021
Onset Date: 01/01/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data: Test Date: 20210129; Test Name: temperature; Result Unstructured Data: Test Result:101 degrees

Allergies:

Symptoms: Joint pain; Soreness in the arm; Temperature went up to like 101 degrees/fever; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received bnt162b2 (BNT162B2), lot number: EH9899, via an unspecified route of administration on 23Jan2021 as single dose for COVID-19 immunization. Medical history included none. There were no concomitant medications. The patient stated he had the COVID shot a week ago and as of now, he has no symptoms until the soreness in the arm but that was natural. The patient had joint pain starting yesterday, day before and today like it was his temperature, it went up to like 101 degrees. The patient was asking if that is normal. The patient stated the fever was today which is 29Jan2021 and still experiencing. The patient took couple Tylenol. The outcome of the event fever was not recovered as of reporting time; while the other events was unknown.

Other Meds:

Current Illness:

ID: 1065424
Sex: U
Age:
State: NC

Vax Date: 01/27/2021
Onset Date: 01/01/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: congested; nauseous; threw up; itchiness; red spots on my arm; I lost my taste and I feel not having taste right now; This is a spontaneous report from a contactable consumer (patient). This patient of unspecified age and gender received dose 2 of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) via an unspecified route of administration on 27Jan2021 as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. Two hours after receiving the vaccine on 27Jan2021, the patient experienced a really bad reaction, itchiness, and red spots on the arm. Around 11:00 on 27Jan2021, the patient got nauseous and threw up. The patient went home and lay down, woke up and lost taste on an unspecified date. The patient felt not having taste "now" on 30Jan2021. On 30Jan2021 the patient was really congested. The outcomes of itchiness, red spots on the arm, nauseous, and threw up were unknown. The outcomes of lost taste and really congested were not recovered. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow-up.

Other Meds:

Current Illness:

ID: 1065425
Sex: F
Age:
State: ID

Vax Date: 01/30/2021
Onset Date: 01/30/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: It seems like she was drunk; it was almost like disorientation like; Had trouble processing like formulating sentences; she had trouble listening and her 'attention' stammered very much; Injection site swelling; Stammer; Pain; This is a spontaneous report from a contactable consumer. This consumer reported for a 26-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number/expiration date: unknown) via an unspecified route of administration on 30Jan2021 at SINGLE DOSE for covid-19 immunisation which was administered by her employer. Medical history was none. There were no concomitant medications. The reporter stated that about 2 hours after the administration of the vaccine "it was almost like disorientation like she was kind of, it seemed like she was drunk. She had trouble processing/formulating sentences. She had trouble listening and her 'attention' stammered very much." No treatment received for reported events. The reporter reported that she seemed better now. The outcome of the reported events was recovering. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1065426
Sex: M
Age:
State: IL

Vax Date: 01/28/2021
Onset Date: 01/28/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Dizzy; nauseous; exhausted; soreness; This is a spontaneous report from a contactable consumer (patient). A 50-year-old male patient, who is 50-year-old the date of vaccination, received bnt162b2 (BNT162B2), lot number: EL8982, via an unspecified route of administration on Arm Left, on 28Jan2021 12:00 as SINGLE DOSE (second dose) for COVID-19 immunization. Medical history included High Blood Pressure. The patient received first dose of bnt162b2 (BNT162B2), lot number=EL3248, on 07Jan2021 at 12:00 on left arm. Concomitant medication included hydrochlorothiazide. On 28Jan2021 12:15, the patient experienced dizzy, nauseous, exhausted, soreness. The outcome of the events was not recovered. No treatment was received for the events. The patient did not have COVID prior vaccination. The patient was not tested post vaccination.

Other Meds: HYDROCHLOROTHIAZIDE

Current Illness:

ID: 1065427
Sex: F
Age:
State:

Vax Date: 01/16/2021
Onset Date: 02/02/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data: Test Date: 20210202; Test Name: Covid-19 virus test; Test Result: Positive

Allergies:

Symptoms: tested positive for the Covid virus on 02Feb; tested positive for the Covid virus on 02Feb.; This is a spontaneous report from a contactable consumer. This consumer reported similar events for 3 patients. This is 3rd of 3 reports. An 89-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on 16Jan2021 at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. Pharmacy technician, calling on behalf of three patients who tested positive after receiving the first dose of the Covid vaccine, asked when they can get the second dose of the Covid vaccine. They received their first dose on 16Jan2021 and tested positive for the Covid virus on 02Feb2021. The outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021138460 same drug/event, different patients

Other Meds:

Current Illness:

ID: 1065428
Sex: F
Age:
State:

Vax Date: 01/28/2021
Onset Date: 01/28/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Sore arm at injection site; chills; fatigue; This is a spontaneous report from a contactable consumer. A non-pregnant 88-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: UNKNONN), via an unspecified route of administration, in the left arm, on 28Jan2021 (at the age of 88 years) as a single dose for COVID-19 immunization. The patient medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19.There were no concomitant medications. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 28Jan2021, the patient experienced sore arm at injection site, chills, fatigue. The patient did not receive any treatment for the sore arm at injection site, chills, fatigue. The clinical outcome of sore arm at injection site, chills, fatigue was recovered. It was also reported that since the vaccination, the patient had not been tested for COVID-19. Information on the lot number has been requested.

Other Meds:

Current Illness:

ID: 1065429
Sex: F
Age:
State: SC

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: 2 days post injection general malaise; Injection site soreness 4 hours post injection; This is a spontaneous report from a non-contactable consumer, the patient. This elderly female patient of unknown age received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number: EL 9265), dose 1 , single dose via an unspecified route of administration in the left arm on 26Jan2021 at 12:00 PM for COVID-19 vaccination. There was no relevant medical history. There were no known allergies. The patient was not pregnant. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications were not reported. The patient did not receive any other vaccine within 4 weeks prior to the vaccine. On 26Jan2021 at 05:00 PM, the patient experienced injection site soreness 4 hours post injection. On 28Jan2021 2 days post injection, the patient had general malaise. No treatment was received for the events. The clinical outcome of injection site soreness and general malaise was recovered on an unknown date. 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: 1065430
Sex: F
Age:
State: OR

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Severe epigastric pain for one hour with nausea, then nausea/queasy/sore abdomen for 24 hours.; Severe epigastric pain for one hour with nausea, then nausea/queasy/sore abdomen for 24 hours.; Severe epigastric pain for one hour with nausea, then nausea/queasy/sore abdomen for 24 hours.; This is a spontaneous report from a non-contactable consumer. A female patient of an unspecified age started received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot Number EK9231); via an unspecified route of administration in the Left arm, on 06Jan2021 at 12:45 as SINGLE DOSE for covid-19 vaccination. Medical history included hypothyroidism. Concomitant medication in two weeks of received vaccine was received (details were not provided). The patient previously took lisinopril and experienced drug hypersensitivity. The facility in which the vaccine was given was a hospital. No other vaccines were given within 4 weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination the patient had not been tested for COVID-19. On 06Jan2021 at 14:00 The patient experienced Severe epigastric pain for one hour with nausea, then nausea, queasy and sore abdomen for 24 hours. Treatment included Zofran sublingual as a result of severe epigastric pain, nausea/queasy and sore abdomen. The clinical outcome of the events Severe epigastric pain was recovered on 06Jan2021 at 15:00 which nausea, queasy and sore abdomen was recovered on 07Jan2021. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1065431
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: Full body chills; This is a spontaneous report from a non-contactable consumer, the patient. A 24-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot unknown, first dose) solution for injection intramuscular in Jan2021 (at the age of 24-years-old) at single dose for COVID-19 vaccination. The patient was not pregnant at the time of vaccination. Medical history included anxiety and depression. Concomitant medication included escitalopram oxalate (LEXAPRO). The patient did not receive any other vaccine within 4 weeks prior to the vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. In Jan2021, the patient experienced full body chills. No treatment was provided for the event body chills. The outcome of the event body chills was recovered in Jan2021. Since the vaccination, the patient has not been tested for COVID-19. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021145063 same reporter/patient/vaccine, different dose/event

Other Meds: LEXAPRO

Current Illness:

ID: 1065432
Sex: F
Age:
State: MO

Vax Date: 12/22/2020
Onset Date: 02/23/2021
Rec V Date: 03/02/2021
Hospital: Y

Lab Data:

Allergies:

Symptoms: multiple bilateral Pulmonary emboli; pulmonary hypertension; short of breath; right heart strain; This is a spontaneous report from a contactable nurse. A 68-year-old female patient received first dose bnt162b2 (PFIZER COVID 19 VACCINE, lot number=EH9899), via an unspecified route of administration at right arm on 22Dec2020 08:00 AM at single dose for COVID-19 immunisation. Medical history included uveitis, arthritis and known allergies: pine nuts. The patient did not have COVID prior vaccination. The patient did not test for COVID post vaccination. The patient was not pregnant. Concomitant medication included prednisone (eye gtt), naproxen as needed (PRN) less than weekly. The patient previously took theophylline and experienced allergies. The day after getting the first dose of vaccine the patient worked all day in another (clinic withheld). She felt well all day, but at 6 pm when she left to go to her car she was so short of breath she had to stop twice to get there. Subsequent work up has shown that she had multiple bilateral Pulmonary emboli resulting in pulmonary hypertension and right heart strain. Adverse event start date was 23Dec2020. Adverse event start time was 06:00 PM. The adverse events resulted in: [Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization for 1 day, Life threatening illness (immediate risk of death from the event)]. Therapeutic measures were taken as a result of the events included Lovenox and Eliquis. The outcome of the event was recovering.; Sender's Comments: Based on available information and known drug profile the reported events are unlikely related to bnt162b2 . These are probably intercurrent medical condition. Case will be reassessed if additional information is received. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds: PREDNISONE; NAPROXEN

Current Illness:

ID: 1065433
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 03/02/2021
Hospital: Y

Lab Data: Test Name: heart beat; Result Unstructured Data: Test Result:racing; Test Name: heart beat; Result Unstructured Data: Test Result:irregular

Allergies:

Symptoms: stroke; blood clot in the heart; Hospitalization with racing and irregular heart beat; Hospitalization with racing and irregular heart beat; loss of motor function; This is a spontaneous report from a non-contactable consumer. A 46-year-old male patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) (brand=Pfizer) on an unspecified date at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. If other vaccine in four weeks was unknown. Other medications in two weeks was unknown. If covid prior vaccination was unknown. If covid tested post vaccination was unknown. Known allergies was unknown. Historical vaccine included the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) (brand=Pfizer) on an unspecified date for COVID-19 immunization. Patient experienced hospitalization with racing and irregular heartbeat, blood clot in the heart, stroke, loss of motor function on an unspecified date. Treatment included intubation. The outcome of the events was unknown. Events resulted in hospitalization, life threatening illness (immediate risk of death from the event). No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

Date Died: 02/18/2021

ID: 1065434
Sex: M
Age:
State: FL

Vax Date: 02/13/2021
Onset Date: 02/18/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Patient died; This is a spontaneous report from a contactable consumer (parent's patient). A 47-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via unknown route on 13Feb2021 (at the age of 47-year-old) at single dose for COVID-19 immunization. Relevant medical history and concomitant medications were not reported. On 18Feb2021 the patient died. The cause of death was unknown. An autopsy was not performed. No COVID prior vaccination. The patient had not been tested for COVID post vaccination. Information about lot/batch number has been requested.; Reported Cause(s) of Death: Patient died

Other Meds:

Current Illness:

Date Died: 01/20/2021

ID: 1065435
Sex: F
Age:
State: NC

Vax Date: 01/19/2021
Onset Date: 01/19/2021
Rec V Date: 03/02/2021
Hospital: Y

Lab Data:

Allergies:

Symptoms: blood clot; death cause: Heart Problems; tired; nauseous; This is a spontaneous report from a contactable consumer. An 81-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot number EL3248), via an unspecified route of administration at single dose in the left arm on 19Jan2021 14:00 for covid-19 immunisation. Medical history included heart problems, pacemaker. Concomitant medication included heparin. The patient experienced death cause: heart problems on 20Jan2021, blood clot on an unspecified date with outcome of unknown that required hospitalization, tired on 19Jan2021 with outcome of unknown, nauseous on 19Jan2021 with outcome of unknown. The patient was hospitalized for blood clot from 16Jan2021 to 18Jan2021. The patient died on 20Jan2021. An autopsy was not performed. The events were described as follows: The patient was tired and nauseous about 3 hours after her vaccine. She had been in the hospital 16Jan2021 to 18Jan2021 for a blood clot. The patient died at her home on 20Jan2021 between 4 and 7 pm. No treatment required. The vaccine was administered at Hospital Facility. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient had not been tested for COVID-19.; Reported Cause(s) of Death: death cause: Heart Problems

Other Meds: HEPARIN

Current Illness:

ID: 1065436
Sex: M
Age:
State: AK

Vax Date: 02/19/2021
Onset Date: 02/20/2021
Rec V Date: 03/02/2021
Hospital: Y

Lab Data: Test Name: Angiogram; Result Unstructured Data: Test Result:Unknown results; Test Name: lab tests; Result Unstructured Data: Test Result:Unknown results; Test Date: 20210221; Test Name: rapid Covid test; Test Result: Negative ; Test Name: CR scan; Result Unstructured Data: Test Result:Unknown results

Allergies:

Symptoms: small heart attack; myocardial/paracardial issues.; My injection location had redness, hardness; My injection location had redness, hardness; pains in chest; headache; chill; running nose; shortness of breath.; This is a spontaneous report from a contactable consumer (patient). A 44-years-old male patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in left arm on 19Feb2021 17:45 at single dose for COVID-19 immunisation at hospital. Medical history included coronary artery disease. The patient's concomitant medications were not reported. The patient previously received the first dose of bnt162b2 on unknown date for covid-19 immunisation. The patient did not have covid before vaccination. The patient experienced small heart attack and myocardial/paracardial issues on an unspecified date with outcome of unknown. These events were serious as life threatening, disability and requiring hospitalization from 21Feb2021 till 23Feb2021 at 14:00. On 20Feb2021 07:00 the patient experienced headache, chill, running nose, shortness of breath with outcome of recovering. The patient experienced also pains in chest on 21Feb2021 11:00 with outcome of recovering and injection location had redness, hardness on an unspecified date with outcome of recovering. Clinical course was as follows. 19Feb2021-5:45pm the patient went to receive vaccine shot. 20Feb2021 the patient had headache, chill, runny nose, and shortness of breath. 21Feb2021 11am still had shortness of breath and pains in chest. Went to clinic had a rapid Covid test come back negative, pain increased and he went to emergency room. The patient was admitted to the hospital with small heart attack and myocardial/paracardial issues. Inflammatory response seems to possibly triggered possible underlying issue of minor heart disease. Then induced heart attack and myocardial issue. The patient would gladly be admitted to a clinic for observation and testing to assist Pfizer in understanding this unfortunate situation. The injection location had redness, hardness. The events resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. The patient received treatment due to the event which included multiple lab tests, Angiogram, CR scan and pain medicine.

Other Meds:

Current Illness: Coronary heart disease

ID: 1065437
Sex: M
Age:
State: WA

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

Lab Data:

Allergies:

Symptoms: large patch of psoriasis on his arm above the elbow, typical psoriasis on his palms and his hands flared; peel crack get nasty; big chunks of skin that crack; Initial information received on 14-Jan-2021 regarding an unsolicited valid non-serious case received from physician. This case is linked to case 2021SA011846. This case involves adult male patient of unknown age who had large patch of psoriasis on his arm above the elbow, typical Psoriasis on his palms and his hands flared (psoriasis), peel crack got nasty (skin exfoliation) and big chunks of skin got crack (skin fissures), after receiving INFLUENZA VACCINE or PNEUMOCOCCAL VACCINE. Medical history, medical treatment(s), vaccination(s), concomitant medication(s) and family history were not provided. On an unknown date, the patient received a dose of suspects INFLUENZA VACCINE produced by unknown manufacturer or PNEUMOCOCCAL VACCINE not produced by Sanofi Pasteur [lot numbers and expiry date not reported] via unknown route in an unknown administration site for prophylactic vaccination. On an unknown date (as reported last year), the patient developed large patch of psoriasis on his arm above the elbow, typical Psoriasis on his palms and his hands flared (psoriasis), peel crack get nasty (skin exfoliation) and big chunks of skin that crack (skin fissures) (non-serious) (Unknown latency), following the administration of INFLUENZA VACCINE and PNEUMOCOCCAL VACCINE. No laboratory data reported. It was not reported if the patient received a corrective treatment. At the time of reporting, the outcome is unknown for all reported events. There will be no information on the batch number to be requested for this case.

Other Meds:

Current Illness:

ID: 1065438
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: feeling icky; still got a sore arm; Initial information was received on 15-Oct-2020 regarding an unsolicited valid non-serious social media case from a consumer via social media. This case involves a patient with unknown demography who experienced icky (Sticky skin) and a sore arm (pain in extremity), while he/she received vaccine INFLUENZA VACCINE. Medical history, past medical treatments, past vaccinations, concomitant medication and family history were not provided. On an unknown date, the patient received a dose of suspect INFLUENZA VACCINE (produced by unknown manufacturer, lot number and expiration date were not reported) via unknown route at an unknown administration site for prophylactic vaccination. On an unknown date, the patient developed a non-serious icky feeling (sticky skin) and a sore arm (pain in extremity), (unknown latency) following the administration of INFLUENZA VACCINE. Laboratory data was not reported. It was not reported if the patient received any corrective treatment. The outcome of both the events was unknown at the time of reporting. There will be no information on the batch number for this case.

Other Meds:

Current Illness:

ID: 1065439
Sex: F
Age: 72
State: OH

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

Lab Data:

Allergies:

Symptoms: Systemic: Dizziness / Lightheadness-Mild

Other Meds:

Current Illness:

ID: 1065440
Sex: M
Age: 88
State: IN

Vax Date: 02/28/2021
Onset Date: 03/01/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Increased [pain, uncontrolled movement of bilateral leg, no appetite,

Other Meds:

Current Illness:

ID: 1065441
Sex: F
Age: 31
State: FL

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data: None known

Allergies: tramadol, peanuts, metal, shellfish, almonds

Symptoms: Back pain 9/10, nausea, dizziness and fever 101 ~14 hours after dose administered

Other Meds: mylan, singular

Current Illness: NOne

ID: 1065442
Sex: M
Age: 98
State: IN

Vax Date: 02/28/2021
Onset Date: 03/01/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Temperature of 100.4 with increased weakness.

Other Meds:

Current Illness:

ID: 1065443
Sex: F
Age: 38
State: FL

Vax Date: 02/26/2021
Onset Date: 02/26/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies: None

Symptoms: Sore arm, severe headache for at least 5 days

Other Meds: Entyvio, Lialda, Daysee, multi vitamin, imitrex

Current Illness: None

ID: 1065444
Sex: F
Age: 69
State: MI

Vax Date: 02/25/2021
Onset Date: 02/26/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data: None

Allergies: Sulfur and Codeine

Symptoms: 22 hours after the vaccination I received almost all of the side effects. They were extreme for 48 hours. They included (fever, head-ache, vomiting, chills, muscle pain, joint pain, swelling and extreme pain in my lymph nodes. Let me note that I am 69 years old with no health conditions. I am not on any medication and in perfect health.

Other Meds: None.

Current Illness: None

ID: 1065445
Sex: F
Age: 81
State: IN

Vax Date: 02/28/2021
Onset Date: 03/01/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Resident noted with emesis x3 on day shift, afrebrile. Resident continues to have small amount of emesis. T. 100.5 went down to 99.6, P. 103 BP. 190/93 O2. 96% Dr. notified. Will continue to monitor.

Other Meds:

Current Illness:

ID: 1065446
Sex: F
Age: 78
State: RI

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

Lab Data:

Allergies:

Symptoms: Patient felt lightheaded and dizzy immediately post vaccination. Observed patient for 30 minutes after which she felt better and left on her own.

Other Meds:

Current Illness:

ID: 1065447
Sex: F
Age: 50
State: NY

Vax Date: 02/27/2021
Onset Date: 02/27/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies:

Symptoms: First dose: Headache for 1 week Second dose: headache, body aches, diarrhea, lethargy

Other Meds:

Current Illness:

ID: 1065448
Sex: F
Age: 79
State: RI

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

Lab Data:

Allergies:

Symptoms: Patient became weak and lightheaded after receiving vaccination. Pt states she ahs had some problems with low blood pressure lately. Observed patient for 30 minutes after which she felt better and left on her own.

Other Meds:

Current Illness:

ID: 1065449
Sex: F
Age: 33
State: GA

Vax Date: 02/23/2021
Onset Date: 02/23/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data:

Allergies: NKDA

Symptoms: EDD 04/15/2021 Pregnancy history: hyperemesis gravitorium POTS pSVT Started feeling bad and fatigued around 9pm. Woke up with chills, severe body aches and bone pain, severe left arm pain, headache, nausea at 11pm. Felt worst I had ever felt in my life. Couldn?t get out of bed due to severe pain. Temp max 101. Lasted until 1pm next day and then resolved however felt tired for several days after and had episodes of tachycardia and pSVT for 2days after (h/o POTS and pSVT and think dehydration from episode with nausea and fever probably caused that)

Other Meds: Aspirin 81mg daily Labatelol 100mg bid Prilosec 20mg bid Zofran odt 4mg PRN Q6hr Phenergan 25mg PRN Q6hr

Current Illness: POTS pSVT runs UTI Dehydration Tachycardia syncope

ID: 1065450
Sex: F
Age: 70
State: KS

Vax Date: 02/16/2021
Onset Date: 02/25/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data: none

Allergies: Codiene, Sensitivity to Epinephrine

Symptoms: Post injection had pain, swelling and redness. After one week it resolved but eight days later on 2/25/21 a rash was noted, red and itchy. I spoke and showed my arm site to the pharmacist and was instructed to ice it and use a topical anti itch cream. The rash is subsiding but not completely resolved at this time3/2/21

Other Meds: Pravastatin, Multi Vitamin, Vitamin D3,

Current Illness: none

ID: 1065451
Sex: F
Age: 33
State: GA

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 03/02/2021
Hospital:

Lab Data: Ultrasound right breast scheduled 03/10/2021

Allergies: Nkda

Symptoms: EDD 04/15/2021 Pregnancy history: hyperemesis gravitorium POTS orthostatic hypotension Mildly sore left arm that afternoon and next day Approximately 2 weeks later developed 2 lumps in right breast awaiting ultrasound to evaluate

Other Meds: Aspirin 81mg Labetolol 100mg bid Prilosec 20mg bid

Current Illness: POTS

ID: 1065452
Sex: F
Age: 57
State: TX

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

Lab Data: ER visit on 2/28/2021 confirmed shingles; Covid test negative, chest Xray clear, CBC was all within range; Ophthalmologist visit 3/1/2021; Rheumatologist visit scheduled for 3/3/2021.

Allergies: Gluten; Penicillin; Sulfa; Cafergot; Dilantin; Keflax/Keflar

Symptoms: Developed severe joint pain and immobility which has affected multiple joints since 2/3/2021 and is still on going. Developed facial and scalp shingles and related low grade fever and flu like symptoms.

Other Meds: Levothyroxine - 88mcg - 1/day; Pantoprazole - 40mg - 1/day;Vitamin D2 - 1.25mg/50,000IU - 1/14 days; Sucralfate 1GM - up to 3/day as needed; Fluticasone nasal spray - 2 sprays per nostril/day; Fluticasone/Salmeterol disk inhaler 250mcg/50mc

Current Illness: Sinus infection

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm