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: 0946062
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: arm hurt; This is a spontaneous report from a Pfizer Sponsored Program. A contactable consumer reported that a patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via unspecified route of administration on unspecified date at single dose for COVID-19 immunization. Patient medical history and concomitant medications were not reported. On unspecified date, the patient experienced arm hurt after getting it. Outcome of the event was unknown. Information about Lot/batch has been requested.

Other Meds:

Current Illness:

ID: 0946063
Sex: U
Age:
State: CA

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

Lab Data:

Allergies:

Symptoms: arm was sore; hard to move without pain; This is a spontaneous report from a contactable nurse. A patient of an unspecified age and gender received first dose of BNT162B2 (Pfizer/ BioNTech Covid-19 vaccine) in dominant arm on an unspecified date in Dec2020 (approximate 24 days ago) at a single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. Within hours that arm was sore and hard to move without pain. Patient could not get keys out of pocket without pain. Pain continued for 12 days. The outcome of the events was unknown. The patient received her second dose on 03Jan2021 in non dominant arm to avoid the lack of mobility. Information about Lot/Batch has been requested.

Other Meds:

Current Illness:

ID: 0946064
Sex: F
Age:
State:

Vax Date: 12/23/2020
Onset Date: 12/01/2020
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: swollen lymph nodes and headache after the first dose; swollen lymph nodes and headache after the first dose; This is a spontaneous report from a contactable other health professional (patient) from a Pfizer Sponsored Program Pfizer First Connect. A 27-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 23Dec2020 at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced swollen lymph nodes and headache on Dec2020. The patient outcome of the events was unknown. Information about Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 0946065
Sex: F
Age:
State: TX

Vax Date: 01/08/2021
Onset Date: 01/10/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: broke out in a rash; This is a spontaneous report from a contactable consumer reporting for herself. A 68-year-old female patient received first dose of bnt162b2 (BNT162B2, lot number and expiry date were not reported), via an unspecified route of administration, on 08Jan2021, at a single dose for COVID-19 immunization. Medical history included chronic obstructive pulmonary disease (COPD) . She had many comorbidities including COPD. Concomitant medications were not reported. The patient broke out in a rash on 10Jan2021. She had a virtual HCP (healthcare professional) appointment and noticed it was on her face. Outcome of the event was unknown. Information on batch number has been requested.

Other Meds:

Current Illness:

ID: 0946066
Sex: M
Age:
State: WV

Vax Date: 01/09/2021
Onset Date: 01/09/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data: Test Name: blood work; Result Unstructured Data: Test Result:Unknown Results

Allergies:

Symptoms: dizziness; he couldn't stand up; he laid down the bed would float; This is a spontaneous report from a contactable consumer (patient). An 81-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3246, expiry: Apr2021), via an unspecified route of administration on 09Jan2021 11:45 at a single dose for COVID-19 immunization. Medical history included retired, he became allergic to penicillin when he was 17 year old and hasn't taken it since, lost his taste and smell, potassium is high sometimes - the doctor recommend he cut down on banana and potatoes, extra heart beat, stomach acid, and thyroid disorder. Ongoing concomitant medications included levothyroxine sodium - has been taking it for a year and a half to two years for thyroid, metoprolol succinate - has been on it about a year and half because an EKG showed he had an extra heart beat, and omeprazole capsule - been on it two or three years for stomach acid. The patient previously took trimethoprim/sulfamethoxazole (BACTRIM) and experienced allergy. After having a Pfizer shot on Saturday, he had a reaction - dizziness. His wife also received the COVID vaccine but did not have any reaction. He sat in the office for 15 minutes like he was supposed to. He drove home and was fine. Two hours later he was so dizzy he couldn't stand up. He was holding onto things to walk through the house. That was two hours after he took the vaccine. After that he thought it would go away in a day. All day yesterday, which was the second day, he was still dizzy. If he laid down the bed would float. It was an awful experience. He received the vaccine at 11:45am on 09Jan2021. Two hours later is when it started. He had to hold onto the rail to get up there. If he gets up quick it is still there. He just had blood work and was due back in Apr for check up. He hasn't had taste and smell for four years or better. He lost his taste and smell and never got it back. He doesn't know what caused that. He hasn't been sick. Outcome of the event dizziness was recovering, for the other events was unknown.

Other Meds: ; ;

Current Illness:

ID: 0946067
Sex: M
Age:
State:

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

Lab Data: Test Name: fever; Result Unstructured Data: Test Result:went up 99.9

Allergies:

Symptoms: fever went up 99.9; woke up covered in sweat; shaking so bad; shivering; had trouble keeping balance; swaying when walking; felt like crap; This is a spontaneous report from a contactable consumer. A 52-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on Dec2020 at a single dose SINGLE DOSE for COVID-19 immunization. Medical history included COVID-19 in Apr2020. The patient's concomitant medications included celecoxib (CELEBREX). After receiving the vaccine fever went up 99.9, woke up covered in sweat, shaking so bad, shivering, had trouble keeping balance, was swaying when he was walking on an unspecified date. The patient also stated he felt ill for 3-4 days. The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds: CELEBREX

Current Illness:

ID: 0946068
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: has a little bit or arm pain and back pain on the side that she received the vaccine; has a little bit or arm pain and back pain on the side that she received the vaccine; This is a spontaneous report from a non-contactable consumer (caregiver). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), via an unspecified route of administration in arm, on an unspecified date, at single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient recently received the vaccine and had a little bit of arm pain and back pain on the side that she received the vaccine on an unspecified date. The reported asked if this was normal and asked if the patient can use acetaminophen to treat pain and some warm compress. The outcome of the events was unknown. No follow-up attempts are possible. Information about Lot/Batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0946069
Sex: M
Age:
State: CT

Vax Date: 01/08/2021
Onset Date: 01/01/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: lymphedema; This is a spontaneous report received from a contactable other healthcare professional (who is also the patient). A male patient of an unspecified age (reported as 47, unit not provided, pending clarification) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), via an unspecified route of administration, on 08Jan2021, at single dose, for COVID-19 immunization, in the hospital. The patient's medical history and concomitant medications were not reported. The patient received his second dose of the COVID19 vaccine on Friday (08Jan2021) and experienced lymphedema as a side effect in Jan2021. The patient would like to know if there is anything he can do for it. The outcome of the event was unknown. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0946070
Sex: F
Age:
State: IN

Vax Date: 01/05/2021
Onset Date: 01/01/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: part of her trunk from the chest down started "itching really bad", and she developed hives; part of her trunk from the chest down started "itching really bad", and she developed hives; she still has a fine rash across the abdomen; there as 6 or 7 little macular spots; This is a spontaneous report from a contactable consumer reported for self. This female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 05Jan2021 at single dose for covid-19 immunisation. She had her first dose of the vaccine last Tuesday 05Jan2021. When at home in Jan2021, part of her trunk from the chest down started "itching really bad", and she developed hives. She took Benadryl, and the itching stopped, but she still has a fine rash across the abdomen, and the hives are still there as 6 or 7 little macular spots. Treatments for the events. Outcome of the event part of her trunk from the chest down started "itching really bad" was recovered in Jan2021. Outcome of the event hives, she still has a fine rash across the abdomen, there as 6 or 7 little macular spots was not recovered. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0946071
Sex: F
Age:
State: FL

Vax Date: 01/07/2021
Onset Date: 01/08/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: feeling fatigue; "just not herself, out of whack in her body"; diarrhea; This is a spontaneous report from a contactable consumer (patient). A 75-year-old female patient received her first dose of bnt162b2 (BNT162B2 reported as Pfizer-Biontech Covid-19 Vaccine; unknown lot number and expiration date), via an unspecified route of administration on 07Jan2021 at a single dose for covid-19 vaccination. The patient's medical history and concomitant medications were not reported. The patient reported that she received the Covid 19 vaccine on 07Jan2021 then the day after (08Jan2021), she began feeling fatigue, "just not herself, out of whack in her body", and diarrhea. The patient reported that she was fine now. She inquired if those were normal. The outcome of the events was recovered on Jan2021. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0946072
Sex: M
Age:
State: FL

Vax Date: 01/06/2021
Onset Date: 01/07/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data: Test Date: 20210109; Test Name: Covid test; Test Result: Positive

Allergies:

Symptoms: coughs once in a while, may be a nervous cough every 40 min; voice hoarse; tested positive for Covid-19; tested positive for Covid-19; didn't feel well at all; bad headache; dry cough; This is a spontaneous report from a contactable consumer who reported for himself, a 70-year-old male patient who received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiration date unknown), 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. The patient stated that he received the first dose of the Pfizer-BioNtech Covid-19 vaccine on Wednesday, 06Jan2021, and on that day he had no problem. On Thursday, 07Jan2021, he started experiencing dry cough. On Friday, 08Jan2021, he didn't feel well at all and had a bad headache. On Saturday, 09Jan2021, he felt better but he tested positive for Covid-19. Today, 11Jan2021, he stated he feels good, he coughs once in a while, may be a nervous cough every 40 min. He had not experienced fever or chills, he breathes well, he can hold his breath for 5-10 seconds, no chest pain or congestion, but his voice was hoarse. Patient wanted to know if this has been reported before, and wanted to know how long should he test himself again for Covid-19. The events were reported as non-serious. The outcome of the events was unknown. Information about lot/batch number is requested.

Other Meds:

Current Illness:

ID: 0946073
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: diarrhea; I had fatigue and weakness; I had fatigue and weakness; This is a spontaneous report from a contactable nurse (patient) received via Medical Information Team. A 44-year-old female patient received the 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 included coeliac disease from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient previously received first 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 reported: "after having the second vaccine, I had fatigue and weakness; the weakness was much greater it seems than what would be considered a normal reaction. I have bad diarrhea and I had to miss work". The patient outcome of the events was unknown. Information on lot number/batch number was requested.

Other Meds:

Current Illness:

ID: 0946074
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: headache; chills; muscle & joint pain; muscle & joint pain; some GI Symptoms (nausea and diarrhea); some GI Symptoms (nausea and diarrhea); injections site soreness; This is a spontaneous report from a contactable pharmacist reported for self. This 46-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 07Jan2021 at single dose for covid-19 immunisation. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) for covid-19 immunisation. She experienced injections site soreness on the day 07Jan2021 then resolved. The next day (08Jan2021) experienced headache, chills, muscle & joint pain, and some GI Symptoms (nausea and diarrhea). Outcome of the event injections site soreness was recovered. Outcome of other events was unknown. Information on batch/lot number was requested.

Other Meds:

Current Illness:

ID: 0946075
Sex: F
Age:
State: MI

Vax Date: 01/08/2021
Onset Date:
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: legs and feet did hurt; Muscle aches are not from flu like; This is a spontaneous report from a contactable nurse reporting for self. This (Age-44, unit-unknown) female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via unspecified route of administration on 08Jan2021 at single dose for COVID-19 immunisation. Medical history included fatigue, she felt fatigue every Friday. Concomitant medications were not reported. The patient stated she got her 2nd vaccine on 08Jan2021, stated "I haven't experienced any side effects, does that mean the vaccine isn't working? " Patient had little fatigue, and stated it's the same fatigue she felt every Friday baseline fatigue. Her legs and feet did hurt, but she had been walking from one end of the hospital to the other. Muscle aches were not from flu like. The outcome of events was unknown. Information about Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0946076
Sex: F
Age:
State: OK

Vax Date: 01/07/2021
Onset Date: 01/09/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: I have redness, swelling and itching at the injection site/pretty red around where she got the shot; I have redness, swelling and itching at the injection site/swollen; I have redness, swelling and itching at the injection site/itches; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 07Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient stated, "I had the 1st Pfizer COVID vaccine on the 07Jan2021; symptoms began on Saturday, 09Jan2021: I have been putting on peroxide on the area. I have redness, swelling and itching at the injection site. Am I doing the right thing?" Her side effects have subsided some, but she still has redness and itching passing. She had her first shot last Thursday and it is pretty red around where she got the shot. It was swollen and it itches. She wanted to know if that was normal. Therapeutic measures were taken as a result of all events. The outcome of the events was recovering. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0946077
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: chest congestion; bother in the throat, at the bottom, me raspa; This is a spontaneous report from a non-contactable consumer (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient reported she was feeling chest congestion and "bother in the throat, at the bottom, me raspa". 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: 0946078
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: pretty bad excruciating, constant headache /constant brain fog headache; pretty bad excruciating, constant headache and fogginess; feeling hung over; This is a spontaneous report from a contactable other health care professional. A 41-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on Jan2021 at single dose for COVID-19 immunization. Medical history included History of migraines. No medication she takes is helping. The patient's concomitant medications were not reported. On Jan2021, the patient has a pretty bad excruciating, constant headache and fogginess, feeling hung over, constant brain fog headache. The outcome of the event was unknown. Information about batch/lot number has been requested.

Other Meds:

Current Illness:

ID: 0946079
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: 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 and expiry date were unknown) via an unspecified route of administration on 30Dec2020 at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient previously took shingles shot (unspecified medication) about 3 or 4 years ago for immunization. The patient stated "I got the Pfizer Vaccine last Wednesday (30Dec2020), then now that "I am in bed" and four days later (Jan2021) my rib cage started hurting on the left side, the side I got the shot on. I went to the doctor and she thought I was starting to have shingles or Intercostal neuritis. I just wondered if the shot could cause you to have shingles." The patient also stated, "I had the shingles shot (unspecified medication) about 3 or 4 years ago. The doctor thought I might have shingles or Intercostal neuritis which is infection in between the ribs." Outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0946080
Sex: F
Age:
State: CA

Vax Date: 12/26/2020
Onset Date: 12/30/2020
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: I was exposed to Covid-19 4 days after and tested + 9 days after dose #1; I was exposed to Covid-19 4 days after and tested + 9 days after dose #1; I was exposed to Covid-19 4 days after and tested + 9 days after dose #1; This is a spontaneous report from a contactable female nurse (patient) via Pfizer sponsored program. A female patient of an unspecified age received bnt162b2 (BNT162B2) on 26Dec2020 at single dose for Covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient was exposed to Covid-19 4 days after on 30Dec2020 and tested + 9 days after dose #1 on 04Jan2021. The outcome of events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Based on the information available, a possible contributory role of the suspect products cannot be excluded for the reported event of positive for corona virus infection for the lack of efficacy of the vaccine. However, based on the mechanism of action of the vaccine, it is unlikely the patient would have fully developed immunity for the vaccine to be effective, due to the number of days passed since the vaccine is given. Case will be reevaluated based on follow-up information

Other Meds:

Current Illness:

ID: 0946081
Sex: F
Age:
State:

Vax Date: 12/30/2020
Onset Date: 12/31/2020
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: she felt very fatigued with a headache; she felt very fatigued with a headache; neck and shoulder pain; neck and shoulder pain; mild dizziness; This is a spontaneous report from a contactable consumer reporting for self. This female patient with unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via unspecified route of administration on 30Dec2020 at single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient stated that she received the first dose of vaccine on 30Dec2020 and the next day (31Dec2020) she felt very fatigued with a headache, neck and shoulder pain, and then experienced mild dizziness. Today (11Jan2021) is the first day that she feels better. She was scheduled to receive the second dose of the vaccine on 20Jan2021 and she wanted to know if she should get the second dose considering her reaction after the first dose. She stated that she used ibuprofen (ADVIL) for the headache and it only helped for about an hour and then she drank Theraflu hot tea and that helped her the most. The outcome of events was recovering. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0946082
Sex: F
Age:
State:

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

Lab Data: Test Date: 202012; Test Name: covid test; Test Result: Positive

Allergies:

Symptoms: positive for covid19; positive for covid19; got or felt sick; This is a spontaneous report from a contactable physician reported for self and consumer. This 51-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on Dec2020 at single dose for covid-19 immunisation. As soon as patient got vaccine she got or felt sick in Dec2020 and had the test and finds out she was positive, so she stays home two weeks and doesn't have no symptom at all and wants to know when has to take a test. The day after the patient developed symptoms thought it was the vaccine, but the symptoms continued for 2-3 days, the 3rd day the patient got herself tested. The patient was positive for covid19 at the time had the shot/ as soon as she got vaccinated she became positive. The patient hasn't had any symptoms for the past 2 weeks. The patient was scheduled to get retested. The patient was scheduled for 2nd dose of vaccine. The patient asked if there are any risks since developed covid the day after getting the vaccine. What if miss today. The patient wanted to know time after having no symptoms past two weeks, when she has to take a test. Outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Test positive for covid19 found as soon as following the vaccination, no adequate effect of the suspect vaccine thus could be reasonably achieved to protect from the targeted infection/disease due to the very short time lag.

Other Meds:

Current Illness:

ID: 0946083
Sex: F
Age:
State: WA

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

Lab Data:

Allergies:

Symptoms: dizziness; swelling in the left cheek in the face; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on an unspecified date at SINGLE DOSE for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, a Consumer calls for information about if she should receive the second dose of the Pfizer's COVID-19 vaccine considering that she developed side effects after the administration of the first dose. The Consumer reported that she had dizziness and swelling in the left cheek in the face. The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0946084
Sex: M
Age:
State:

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

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

Allergies:

Symptoms: I've got the 1st dose of vaccine and then unfortunately, in the interim, I started feeling sick and tested positive for Covid.; I've got the 1st dose of vaccine and then unfortunately, in the interim, I started feeling sick and tested positive for Covid.; This is a spontaneous report from a Pfizer-sponsored program, received from a contactable consumer (patient). A male patient of an unspecified age received his first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiry date were not provided) solution for injection, 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 reported he got the 1st dose of the vaccine and then unfortunately, in the interim, he started feeling sick and tested positive for Covid. The patient underwent Covid test and resulted positive on an unknown date. Outcome of the event was unknown. No follow-up activities are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 0946085
Sex: U
Age:
State:

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

Lab Data: Test Name: corona; Result Unstructured Data: Test Result:positive; Comments: corona positive after a week

Allergies:

Symptoms: 13 people, who were applied the vaccine previously, were corona positive after a week; 13 people, who were applied the vaccine previously, were corona positive after a week; This is a spontaneous report from a non-contactable consumer. This consumer reported similar events for 13 patients. This is 12th of 13 reports. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; lot number and expiration date: not known), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that 13 people, who were applied the vaccine previously, were corona positive after a week on an unspecified date. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021018407 same reporter, similar suspect drug and event; different patient

Other Meds:

Current Illness:

ID: 0946086
Sex: F
Age:
State: CA

Vax Date: 12/23/2020
Onset Date: 01/01/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data: Test Date: 20210101; Test Name: COVID-19 virus test; Test Result: Positive

Allergies:

Symptoms: Positive COVID-19 test with symptoms; Positive COVID-19 test with symptoms; This is a spontaneous report from a Pfizer-sponsored program, from a contactable nurse (patient). A 35-year-old female patient (weight 55.79 kg, height 160 cm) received the first dose of BNT162B2 (Pfizer-Biontech Covid-19 Vaccine, Lot. EK5730) intramuscularly, in the left deltoid, at single dose, on 23Dec2020 at 12:30, for COVID-19 immunisation. The patient had not received any other vaccines within 4 weeks prior to the BNT162B2 vaccine. Relevant medical history and concomitant medications were none. On 25Dec2020, the patient felt extremely tired (fatigue). On 28Dec2020, the patient had headache and minor cough noticed. On 29Dec2020, the patient experienced back pain and she said that it felt like sunburn soreness more than anything else. She said that she literally slept 3 days in a row (29Dec2020, 30Dec2020, and 31Dec2020). On 31Dec2020, the patient lost her sense of smell and developed dizziness. On 01Jan2021, the patient experienced nausea and lost her sense of taste. COVID-19 virus test was found positive on 01Jan2021.The patient recovered from back pain, sunburn and sleepy on 31Dec2020, recovered from tiredness on 01Jan2021, recovered from nausea and dizziness on 06Jan2021. Clinical outcome of the events, smell loss, cough, headache, and loss of taste was recovering. Final clinical outcome of positive COVID-19 test with symptoms was unknown at time of this report. The case was assessed as serious (medically significant). She is scheduled to get 2nd dose of BNT162B2 (Pfizer-Biontech Covid-19 Vaccine) on 13Jan2021 and is wanting to know if she is supposed to get it.; 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: 0946087
Sex: F
Age:
State: CT

Vax Date: 01/09/2021
Onset Date: 01/09/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chills, myalgia, axillary lymphadenopathy; Chills, myalgia, axillary lymphadenopathy; Chills, myalgia, axillary lymphadenopathy; This is a spontaneous report from a contactable other HCP. A 35-year-old female patient started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231), via an unspecified route of administration (anatomical location: arm right) from 09Jan2021 to 09Jan2021 at single dose for COVID-19 immunisation. Medical history was reported as none. The patient had first vaccine on 18Dec2020 to 18Dec2020 for COVID-19 immunisation. The patient's concomitant medications were not reported. On 09Jan2021, the patient experienced chills, myalgia, axillary lymphadenopathy. The patient did not received any treatment for the events. Outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 0946088
Sex: F
Age:
State: MN

Vax Date: 12/21/2020
Onset Date: 01/08/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data: Test Date: 20210108; Test Name: fever; Result Unstructured Data: Test Result:102.9; Test Date: 20210108; Test Name: fever; Result Unstructured Data: Test Result:99.7; Test Date: 20210108; Test Name: fever; Result Unstructured Data: Test Result:99.9

Allergies:

Symptoms: neck sore to left shoulder and over to right ear; Fever; right ear ache/neck sore to left shoulder and over to right ear; left arm sore; neck sore to left shoulder and over to right ear; This is a spontaneous report from a contactable consumer. A 52-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), Batch/lot number EK4176, Expiry Date: Mar2021, via an unspecified route of administration on 21Dec2020 at a SINGLE DOSE then via an unspecified route of administration on 07Jan2021 at a SINGLE DOSE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient's husband was calling for his wife that had the second shot. He stated that she was a nurse. He stated that she came home from work with her arm and neck sore. He stated that the neck soreness was causing ear ache. He stated that her fever was 102.9 and stated that they put a cool rag on her head. He stated that she had the shot yesterday and stated that she had her first shot 21Dec2020. They stated that arm sore at 1:00 in morning and stated sore neck at 11:30 this morning. Fever started at 11:30 and was 99.7 and about 15 minutes later was 99.9 and stated that was with having three Aleves. She stated that it is back up to 102.9 and stated that the right ear ache started at 11:00am today. The patient underwent lab tests and procedures which included body temperature: 102.9 on 08Jan2021, 99.7 on 08Jan2021 and 99.9 on 08Jan2021. Therapeutic measures were taken as a result of fever (pyrexia). The outcome of events was not recovered.

Other Meds:

Current Illness:

ID: 0946089
Sex: U
Age:
State: NJ

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

Lab Data: Test Name: COVID019; Result Unstructured Data: Test Result:positive; Comments: tested positive for Covid 10 days after

Allergies:

Symptoms: Received Covid vaccine and tested positive for Covid 10 days after; Received Covid vaccine and tested positive for Covid 10 days after; 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 date were not reported), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received COVID vaccine and tested positive for COVID, 10 days after on an unspecified date. The patient underwent lab tests and procedures which included sars-cov-2 test: positive on an unspecified date. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0946090
Sex: F
Age:
State: IL

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Second dose: fever, chills, muscle and joint pain, headache, fatigue; Second dose: fever, chills, muscle and joint pain, headache, fatigue; Second dose: fever, chills, muscle and joint pain, headache, fatigue; Second dose: fever, chills, muscle and joint pain, headache, fatigue; Second dose: fever, chills, muscle and joint pain, headache, fatigue; Second dose: fever, chills, muscle and joint pain, headache, fatigue; This is a spontaneous report from a contactable other HCP. A 28-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) at left arm, via an unspecified route of administration on 08Jan2021 13:00 at single dose for covid-19 immunisation. Medical history included postural orthostatic tachycardia syndrome. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient previously received first dose of bnt162b2 (anatomical Location: Arm Left) on 18Dec2020 09:30 and experienced headache, arm pain. Concomitant medication included spironolactone and metoprolol. The patient experienced events after the second dose: fever, chills, muscle and joint pain, headache, fatigue on 08Jan2021 21:00. No treatment was received for the adverse events. Since the vaccination, the patient has not been tested for COVID-19. The outcome of events was recovering. Information about lot/batch number has been requested.

Other Meds: ;

Current Illness:

ID: 0946091
Sex: F
Age:
State: GA

Vax Date: 12/30/2020
Onset Date: 01/07/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: soreness in her arm at the injection site in the left arm; bruising at injection site; injection site that is red and hot; itching and redness at injection site; itching and redness at injection site; This is a spontaneous report from a contactable consumer (patient). A 94-year-old female patient received BNT162B2 (Lot/batch number and expiry date unknown), via an unspecified route of administration from 30Dec2020 to 30Dec2020 at SINGLE DOSE in the left arm for COVID-19 immunization. There were no medical history and concomitant medications. The patient stated that she got the Covid vaccine a week ago on Wednesday, 30Dec2020, 9 days ago, stated she did not seem to have any problems or side effects after, then she felt some soreness in her arm at the injection site in the left arm. States that last night on 07Jan2021, she woke up itching and redness at injection site and when she looked at her arm this morning, there is a really bad 2 1/2 to 3 inches at the injection site that is red and hot. Also she experienced bruising at injection site. She wants to know if this is a common thing. The outcome of the event "bruising at injection site" was recovering; for events Vaccination site pruritus and Vaccination site erythema was recovered on unknown dates; while unknown for the other events. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0946092
Sex: F
Age:
State: IL

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

Lab Data:

Allergies:

Symptoms: sleeping all day; pain at the injection site to left arm; Fever; Headache; legs hurting; This is a spontaneous report from a contactable consumer (patient). A 46-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EJ1685), via an unspecified route of administration in the left arm on 07Jan2021 at a single dose for COVID-19 immunization. There were no medical history and concomitant medications. The patient previously took the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on Dec2020 (reported as three weeks ago from 07Jan2021) for COVID-19 immunization and she was fine. The patient got the second COVID vaccine on 07Jan2021 afternoon. The pain at the injection site to left arm started on 07Jan2021 20:00. On 07Jan2021, in the middle of the night, the fever, headache, and legs hurting started. She has been sleeping all day on 08Jan2021 and she does not do this normally. Outcome of the sleeping all day was unknown, of the headache was recovering, of the pain at the injection site to left arm was recovered on 07Jan2021, of the legs hurting and fever was recovered on 08Jan2021.

Other Meds:

Current Illness:

ID: 0946093
Sex: F
Age:
State: IL

Vax Date: 01/08/2021
Onset Date: 01/10/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Dizziness; This is a spontaneous report from a contactable nurse (patient herself). A 43-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection; lot number: EL1283, expiration date was unknown), via an unspecified route of administration on the left arm on 08Jan2021 at 17:00 at a single dose for COVID-19 immunization. The patient received her first dose of bnt162b2, via an unspecified route of administration on the left arm on 19Dec2020 at 13:00. Both doses were administered at the hospital. The patient had no medical history. The patient had no known allergies; she had no allergies to medications, food, or other products. Concomitant medication included unspecified multivitamins. The patient was not pregnant at the time of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the was not patient diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient experienced dizziness on 10Jan2021 at 20:00, or 24 hours after the shot had been given. At the time of the report, at the 12 hour mark, she was still being dizzy. The reporter assessed the event as non-serious. The patient did not receive any treatment for the adverse event (AE). The patient was not recovered from the event.

Other Meds:

Current Illness:

ID: 0946094
Sex: F
Age:
State: FL

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

Lab Data: Test Date: 20210106; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: Light headache ( first day); nausea ( 3 days); severe fatigue (2 days); This is a spontaneous report from a contactable healthcare professional (patient). A 53-years-old female patient received first dose on bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number Bj1685, expiration date not reported), intramuscular, on the left arm, on 07Jan2021 at 15:00 at a single dose for Covid-19 immunization. Medical history included scleroderma, interstitial lung disease (ILD), and Raynauds. The patient's concomitant medications were not reported. The patient previously took erythromycin and experienced allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient is not pregnant. On 06Jan2021, the patient had a nasal swab with negative result. On 07Jan2021, the patient experienced light headache (first day), nausea (3 days) and severe fatigue (2 days). The patient had a nasal swab with negative result on 06Jan2021. The patient did not receive treatment for the adverse events. The outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 0946095
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Not feeling well; Slight flu; Fatigue; This is a spontaneous report from a Pfizer-sponsored program. A non-contactable consumer (patient) reported that a female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) on 07Jan2021 at a single dose, with route of administration unspecified, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. In Jan2021, the patient was not feeling well; had a slight flu; and fatigue. The outcome of the events, 'not feeling well', 'slight flu' and 'fatigue', was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0946096
Sex: F
Age:
State: NJ

Vax Date: 12/16/2020
Onset Date: 12/20/2020
Rec V Date: 01/15/2021
Hospital: Y

Lab Data: Test Date: 20210109; Test Name: covid test; Test Result: Negative

Allergies:

Symptoms: started with left sided lower back pain; This is a spontaneous report from a contactable Nurse (patient). A 22-year-old female patient received the first dose of BNT162B2 (lot number: EH9899), via an unspecified route of administration at left arm on 16Dec2020 13:45 at single dose for covid-19 immunization. Medical history included allergies for All fish. The patient's concomitant medications were not reported. The patient had the first covid vaccine on 16Dec2020 and on 20Dec2020 started with left sided lower back pain. The event resulted in Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization (2 days), Life threatening illness (immediate risk of death from the event). The patient received the Heparin drip and xarelto at home for the event. The patient was not pregnant. The patient received the covid test post vaccination on 09Jan2021. Test type was Nasal Swab. The result was negative. The outcome of the event was recovered with sequel on unspecified date.; Sender's Comments: From the information provided it is unclear what is the nature of the reported event and what are the reasons that have put the subject at immediate risk of death. The event is considered possibly related to the suspect product based on the positive temporal association.

Other Meds:

Current Illness:

ID: 0946098
Sex: F
Age:
State: MD

Vax Date: 01/09/2021
Onset Date: 01/10/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: throat closing up; struggled the breath; This is a spontaneous report from a contactable consumer (patient). A 44-year-old female patient (non-pregnant) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: Pfizer EL 3302), via an unspecified route of administration on 09Jan2021 07:30 am at single dose at left arm for covid-19 immunization. Medical history included diabetes, high blood pressure, allergies. The patient's concomitant medications were not reported. Patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, patient has not been tested for COVID-19. On 10Jan2021 14:30, patient woke up with throat closing up and struggled the breath. Patient immediately drank a dose of diphenhydramine hydrochloride (BENADRYL). Patient did that two more time in the evening of 10Jan2021. Patient called the doctor in the morning. Events were considered serious per life-threatening. The adverse events resulted in doctor or other healthcare professional office/clinic visit, life threatening illness (immediate risk of death from the event). Patient received treatment liquid diphenhydramine hydrochloride, epinephrine (EPI-PEN) for events. Outcome of events was recovered in Jan2021.

Other Meds:

Current Illness:

ID: 0946099
Sex: F
Age:
State:

Vax Date: 01/09/2021
Onset Date: 01/09/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Pain at injection site; Headache; Nausea; Vomiting; Loss of appetite; Fatigue; Chills; This is a spontaneous report from a non-contactable nurse (patient herself). This 35-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EL3248), via intramuscular, on 09Jan2021 at 10:30, at single dose in the left arm, for COVID-19 immunisation. The patient was not pregnant. She was vaccinated at hospital, age at vaccination was 35-year-old. The patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EL5730), via intramuscular, on 19Dec2020 at 13:00 at single dose in the right arm. Historical vaccine includes Hepatitis A vaccine (single dose, via an unknown route in the arm left) on 18Dec2020. No medical history was provided. No known allergies. No relevant concomitant medications were provided. The patient was vaccinated at hospital, age at vaccination was 35-year-old. Pre-vaccination and post-vaccination COVID tests were not performed. On 09Jan2021 at 18:00, the patient developed pain at injection site, headache, nausea, vomiting, loss of appetite, fatigue, and chills. The patient was not treated for the events. The patient had recovered from the events on unknown date in Jan2021. No follow-up attempts are possible. No further information expected.

Other Meds:

Current Illness:

ID: 0946100
Sex: F
Age:
State: IL

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

Lab Data:

Allergies:

Symptoms: Lymphadenopathy; Patient that was 13 weeks pregnant did receive the first dose; This is a spontaneous report from a Pfizer-sponsored program, PFIZER FIRST CONNECT. A contactable physician reported that a female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) at a single dose, with route of administration and therapy date unspecified, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient was 13-week pregnant when the first dose of the vaccination was received. On an unspecified date, the patient had lymphadenopathy. The outcome of the events, '13-week pregnant when the first dose of the vaccination was received' and 'lymphadenopathy', was unknown. The patient was asking about the second dose of the vaccine. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0946101
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: the spot itched like crazy; This is a spontaneous report from a contactable consumer via a Pfizer-sponsored program. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), via an unspecified route of administration, on an unspecified date, at single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced "the spot itched like crazy" on an unspecified date. The outcome of the event was unknown. Information about lot/batch has been requested.

Other Meds:

Current Illness:

ID: 0946102
Sex: M
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: my husband, an hour after, got a really bad headache; This is a spontaneous report from a non-contactable consumer (patient's wife). A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. It was reported that the patient (husband) got a really bad headache an hour after, got a really bad headache and still cannot get rid of the headache The outcome the event was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0946103
Sex: F
Age:
State: IL

Vax Date: 01/09/2021
Onset Date: 01/10/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: chills; body aches; fever; flu like symptoms; headache; was drenched in sweat; This is a spontaneous report from a contactable nurse (patient). A 46-year-old female patient received the second dose of BNT162b2 (lot: EL1283), via an unspecified route of administration in left deltoid on 09Jan2021 15:30 at single dose for covid-19 immunization. Medical history included asthma from Dec2019 and ongoing, insomnia, hypertension. Concomitant medication included ongoing hydrochlorothiazide, metoprolol tartrate (LOPRESSOR HCT) for Hypertension. The patient previously took lopressor and experienced edema. The patient previously received the first dose of BNT162b2 (Lot number: EK5730), intramuscularly in right deltoid at single dose on 19Dec2020 for covid-19 immunization. The patient experienced fever, chills, flu like symptoms, headache all day long on 10Jan2021. The above events were reported as serious as medical significant. No nausea or diarrhea. She had chills and was drenched in sweat on 10Jan2021. She woke up at 10:30 am with chills, body aches on 10Jan2021. Last night at 10 pm she finally fell asleep. She woke up this morning (11Jan2021) and felt fine. The outcome of the event sweating was unknown, other events was recovered on 11Jan2021.; Sender's Comments: Based on a close temporal relationship there is a reasonable possibility of an association between the events and the product. 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: LOPRESSOR HCT

Current Illness: Asthma

ID: 0946104
Sex: F
Age:
State: OH

Vax Date: 12/18/2020
Onset Date: 12/18/2020
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: she had a stiff neck; This is a spontaneous report from a contactable consumer (patient). A 57-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EK5730), via an unspecified route of administration on 18Dec2020 at a single dose on the left arm for COVID-19 immunization. Medical history was reported as none. There were no concomitant medications. Patient received the first dose of vaccine on 18Dec2020 and reported that she had a stiff neck for two days. The outcome of the event was recovered on 20Dec2020. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0946105
Sex: F
Age:
State: MA

Vax Date:
Onset Date: 01/08/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Localized pain at injection site; pain in her arm pit to the touch and when she moves it; This is a spontaneous report from a contactable consumer. A 28-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; lot number: EK9231, Expiry: Apr2021); via unspecified route of administration on an unspecified date at single dose at left arm for covid-19 immunisation. There was no medical history and concomitant medications reported. The patient previously had BNT162B2 for COVID-19 immunization and experienced localized pain at injection site. Stated that the patient got the 2nd dose of the Covid-19 vaccine on an unspecified date (reported as Friday). She didn't have a fever or chills, but she did have localized pain at injection site which she also had with the first dose. She is calling because she still has pain in her armpit, to the touch and when she moves it reported on 08Jan2021, but there is no swelling, lumps or bumps. The patient stated that the pain has decreased; it's not as bad as it was when she first noticed it. The patient got the 2nd dose at 5:30pm, and had pain at around 8pm or 9pm that night. The following day was the height of the pain for the second dose, and it has been decreasing since then. The outcome of the event localized pain at injection site was unknown, while recovering for the event pain in her arm pit to the touch and when she moves it.

Other Meds:

Current Illness:

ID: 0946106
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: felt a little stuffy; sick; This is a spontaneous report from a contactable nurse. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: unknown), 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. This Nurse reported information regarding a coworker. The patient felt a little stuffy and mentioned that no one was sick like her; no one else missed work; they all went around the same dates to get the vaccine because they work in home health kind of roles; so they did not all get them at the same time like if they were in a facility. The outcome of the events was unknown. Information about Lot/Batch number is requested.

Other Meds:

Current Illness:

ID: 0946107
Sex: U
Age:
State: NJ

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

Lab Data: Test Name: Platelets; Result Unstructured Data: Test Result:High

Allergies:

Symptoms: High platelets; This is a spontaneous report from a contactable healthcare professional. This healthcare professional reported similar events for two patients. This is second of two reports. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number and Expiration Date were not reported), via an unspecified route of administration, on an unspecified date, at a single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The physician (through the healthcare professional) would like to know if the company had any reports of thrombocytosis post vaccination. The physician had seen two patients who had high platelets after the vaccine on an unspecified date. There is no reported platelet value for this patient. The healthcare professional has no information on the patient since the physician only asked her to call. The outcome of the event was unknown. Information about lot number and expiration date for the suspect product will be requested in follow-up attempts.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021017585 Same reporter, product, and event; different patient

Other Meds:

Current Illness:

ID: 0946108
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Headache; This is a spontaneous report from the Pfizer Sponsored Program received by a contactable consumer (patient husband). A female patient (age not provided) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unknown route, on 10Jan2021 at single dose for COVID-19 immunisation. No relevant medical history and concomitant medications were provided. In Jan2021, after vaccination, the patient developed headache. The reported asked if she could take acetaminophen. The outcome of the event was unknown. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0946109
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: a bit of a headache for the second dose; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received 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. The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: not reported) on an unspecified date for COVID-19 immunization and experienced slight swelling. The patient had taken both doses of the Pfizer COVID vaccine and did not experience any side effects like the everybody else. She stated that she is concerned since everyone she had talked to who received the vaccine experienced some kind of side effects (fever, chills, body ache) and was wondering if the vaccine might not be working. She only experienced a bit of a headache for the second dose. Outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0946110
Sex: F
Age:
State:

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Pain in her right arm near injection site/ pain in her right arm near injection site is very achy or tender; sore; she was hurting so much needed an ice pack/pain goes down kind of to her underarm/armpit; when she touches the area she can feel the soreness all the way down to her armpit; radiating pain; pneumonia shot given on 08Jan2021 was the second dose for pneumonia shot; This is a spontaneous report from a contactable consumer (patient). A 66-year-old female patient received second dose of pneumococcal 13-valent conjugate vaccine (diphtheria CRM197 protein) (lot number and expiration date unknown) via unspecified route of administration on 08Jan2021 at single dose (either left or right arm; not sure which arm) for immunization; and influenza vaccine via unspecified route of administration on 08Jan2021 at single dose for immunization. Medical history included knee arthroplasty from Nov2020 to Nov2020 (not ongoing). Concomitant medications included ibuprofen at unknown dose (500mg or 600mg as needed-not sure which strength/dose), as needed for pain; and paracetamol (TYLENOL) at unknown dose (500mg or 600mg as needed-not sure which strength/dose), as needed for pain. The patient previously received influenza vaccine (flu shot) last year, 2020 for immunization (stated she received flu shot yearly); no event occurred in that past vaccination. Patient also previously received first dose of pneumococcal 13-valent conjugate vaccine (diphtheria CRM197 protein) (referred as pneumonia shot) in 2020 for immunization. It was reported that patient got influenza vaccine (flu shot) and pneumonia shot on 08Jan2021. On 09Jan2021, she had onset of pain in her right arm near injection site. Patient does not know which arm the flu shot and pneumonia shot were administered; she just got one in each arm; cannot specify which. Names on the products cannot be clarified at this time. Patient stated she got the first dose of pneumonia shot last year which was given at her doctor's office, not the pharmacy and she did not have this event with that shot; this pneumonia shot given on 08Jan2021 was the second dose for pneumonia shot. It was clarified that pain in her right arm near injection site did not start right away on 08Jan2021; it started the next day. Further described as: Last night, 08Jan2021, she was hurting so much needed an ice pack; she clarified that it was not sore at that time; it was pain. The pain goes down kind of to her underarm/armpit; when she touches the area she can feel the soreness all the way down to her armpit; radiating pain. She knew it would feel achy and warm a little bit; but not like this pain. She started feeling like maybe the Pharmacist did not give her the shot right. Right now, 09Jan2021, the pain in her right arm near injection site is very achy or tender; sore; but not like it was last night. She does not feel anything wrong on the left arm where the other product injection was given (cannot determine which product). Outcome of the event (pain in right arm near injection site) was recovering; outcome of other event was unknown. Pfizer is a marketing authorization holder of Pneumococcal 13-valent conjugate vaccine (diphtheria CRM197 protein) in the country of incidence or the country where the product was purchased (if different). This may be a duplicate report if another marketing authorization holder of Pneumococcal 13-valent conjugate vaccine (diphtheria CRM197 protein) has submitted the same report to the regulatory authorities. No follow-up attempts are needed. No further information is expected; information about batch number cannot be obtained.

Other Meds: ; TYLENOL

Current Illness:

ID: 0946111
Sex: F
Age:
State: NY

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data: Test Date: 2020; Test Name: COVID-19 antibody test; Result Unstructured Data: Test Result:Negative; Test Date: 2020; Test Name: COVID-19 antibody test; Result Unstructured Data: Test Result:Negative; Test Date: 2020; Test Name: COVID-19 antibody test; Result Unstructured Data: Test Result:Negative; Test Date: 202011; Test Name: COVID-19 antibody test; Result Unstructured Data: Test Result:Negative

Allergies:

Symptoms: Hives; Left arm 0.3mL/ sore ness on the arm Left; This is a spontaneous report from a contactable consumer (patient). A 42-year-old (also reported as "41") female patient received the first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EL3248, Expiry Date: 30Apr2021, 3 mcg/ml), via an unspecified route of administration on 08Jan2021 08:40 at 0.3 mL, single dose at left arm ("Dosage text: Left arm 0.3mL") for COVID-19 immunization. Medical history included asthma. Concomitant medication included fluticasone furoate, vilanterol trifenatate (BREO ELLIPTA, reported as "BREO") for asthma. The patient was given 0.3mL, 30mcg of the COVID vaccine. The patient experienced sore ness on the arm left on 08Jan2021 and hives on 09Jan2021. She is calling about the Covid Vaccine, she got it on Friday 08Jan2021 at 8:40AM and she went home got soreness in arm (began the same day), it was a couple hours after at 10 or 11 and it stopped on Sunday 10Jan2021. She took pain killers. She woke up Saturday morning, and her whole body has broken out in hives, she has been taking Benadryl around the clock. She broke out in hives on 09Jan2021, it is still ongoing, its in between, she is still scratching and taking the Benadryl. Therapeutic measures were taken as a result of the events which included pain killers and Benadryl. The outcome of the event sore ness on the arm left was recovered on 10Jan2021, of hives was not recovered. She has never had a positive test for COVID prior to the vaccine. She has had an Antibody test 4 times and each time it was negative, she had her last antibody test in Nov2020. She has had no issues with vaccines in the past.

Other Meds: BREO ELLIPTA

Current Illness:

ID: 0946112
Sex: F
Age:
State: AK

Vax Date: 01/08/2021
Onset Date: 01/09/2021
Rec V Date: 01/15/2021
Hospital:

Lab Data:

Allergies:

Symptoms: muscle aches; fever; nausea; Vomiting; This is a spontaneous report from a contactable other healthcare professional (patient). A 40-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), lot number: EL3246, intramuscular right arm from 08Jan2021 to 08Jan2021 as single dose for COVID-19 immunisation. Historical vaccine includes first dose of BNT162B2 via intramuscular from 18Dec2020 to 18Dec2020 with lot number: EJ1685 on right arm. Medical history included allergies to sulfa drugs. Concomitant medication included metronidazole. The patient previously took Ciprofloxacin and Codeine and experienced allergies. On Saturday, 09Jan2021 at 07:00 AM, the patient developed fever, muscle aches, nausea, and vomiting. The outcome of the events was recovered on Jan2021. No treatment was given for the events. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm