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: 1000005
Sex: F
Age:
State: OK

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

Lab Data:

Allergies:

Symptoms: stated she felt broke, clarified she was having all over joint pain that was very bad; no control of her kidneys/she has messed the bed up twice since yesterday; This is a spontaneous report from a contactable consumer, reporting for herself. A 90-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date were not reported), via an unspecified route of administration on 14Jan2021 at a single dose for COVID-19 immunization. Medical history included ongoing urinary incontinence (stated she has always had a little trouble). There were no concomitant medications. The patient got a shot yesterday, 14Jan2021, stated she felt broke, clarified she was having all over joint pain that was very bad, stated she has no control of kidneys, states she has always had a little trouble, but since yesterday it just wont stop, stated she has messed the bed up twice since yesterday. She was taking Tylenol for the pain and that was all she knows to do. She was encouraged to reach out to her HCP for any medical advice if she has concerns. The outcome of the events was not recovered. Information on the batch/lot number has been requested.

Other Meds:

Current Illness: Urinary incontinence (stated she has always had a little trouble)

ID: 1000006
Sex: F
Age:
State:

Vax Date: 12/28/2020
Onset Date: 01/04/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210104; Test Name: covid; Test Result: Positive

Allergies:

Symptoms: tested positive for covid; tested positive for covid; This is a spontaneous report from a Pfizer-sponsored program. A contactable Other Health Professional (patient) reported that a female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) lot number and expiry date unknown, via an unspecified route of administration on 28Dec2020 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications was not reported. It was reported that the patient got the first dose of vaccine 28Dec2020 and tested positive for COVID on 04Jan2021 but mentioned that her quarantine period is already over. She stated that she is scheduled to get the 2nd dose of the vaccine tomorrow, but wants to know if she should still proceed to receiving it. The patient underwent lab tests and procedures which included covid: positive on 04Jan2021. The outcome of the events was unknown. Information on lot/batch number has been requested.; Sender's Comments: Based on the mechanism of action of BNT162B2 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 was given (7 days in this case). However, a causal relationship between event "tested positive for Covid " (coded to Drug ineffective / SARS-CoV-2 test positive) and BNT162B2 vaccine cannot be completely excluded.

Other Meds:

Current Illness:

ID: 1000007
Sex: M
Age:
State: WI

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

Lab Data: Test Date: 20210114; Test Name: Blood sugar; Result Unstructured Data: Test Result:250-300; Comments: 8-10 hours agter getting the vaccine his blood sugar was out of control ranging from 250-300; Test Date: 20210115; Test Name: Blood sugar; Result Unstructured Data: Test Result:207; Comments: He took it when he woke and it was 207; Test Date: 20210115; Test Name: Blood sugar; Result Unstructured Data: Test Result:242; Comments: Two hours after eating a light breakfast it was 242

Allergies:

Symptoms: blood sugar has been out of control ranging from 250-300; This is a spontaneous report from a contactable consumer. A 53-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiration date not reported), via an unspecified route of administration, on the right arm, on 14Jan2021 at a single dose for Covid-19 immunization. Medical history included type 2 diabetes mellitus from Sep2019 and ongoing. There were no concomitant medications. On 14Jan2021, it was reported that 8-10 hours after getting the vaccine, his blood sugar was out of control ranging from 250-300. On 15Jan2021, he has taken his blood sugar twice at the time of report. He took it when he woke and it was 207. Two hours after eating a light breakfast it was 242. The outcome of the event was not recovered. Information about lot/batch number has been requested.

Other Meds:

Current Illness: Type 2 diabetes mellitus

ID: 1000008
Sex: F
Age:
State: CA

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

Lab Data:

Allergies:

Symptoms: little tachycardic; I felt anxious about what I was feeling; she felt her lip and cheek tingling; felt kind of itchy but under her skinitchy sensations all over her body that come and go; felt a quick weird sensation under scapula; tingling sensation going down the side of her back that she got the vaccine on/all of her left side was tingling/woke up to a weird tingling all over her body/tingling on her hands; This is a spontaneous report from a contactable other health professional. An adult (18-64 years) female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), (lot number: EL3248) via an unspecified route of administration, in the left arm, on 18Jan2021 07:45 at SINGLE DOSE for COVID-19 immunization. Medical history included asthma. Patient had BNT162B2 on 28Dec2020 in the left arm for COVID-19 immunization (first dose with lot number: EL1284). Concomitant medication included ibuprofen, fluticasone propionate, salmeterol xinafoate (ADVAIR), cetirizine hydrochloride (ZYRTEC), fluticasone propionate (FLONASE) and norethisterone (NORA-BE). On 18Jan2021 08:00, about 15 min after vaccination, the patient felt a quick weird sensation under scapula and a tingling sensation going down the side of her back that she got the vaccine on. Maybe 30 min after vaccine (18Jan2021, 08:15), she felt her lip and cheek tingling. An hour after (08:45), all of her left side was tingling and felt kind of itchy but under her skin. She had just finished working night shift and fell asleep. She slept 9 hours and woke up to a weird tingling all over her body. She was a little tachycardic because she felt anxious about what she was all feeling (19Jan2021). Once she had calm herself down, her heart rate was back to her baseline. She had no difficulty breathing, no rashes, and otherwise felt fine. She had dinner and was awake for few hours before sleeping another 8 hours. It was now about 33 hours after and she still have random tingling/itchy sensations all over her body that come and go and tingling on her hands that has never stopped. No follow-up attempts are possible. No further information is expected. Information on the lot/batch number has been obtained.

Other Meds: IBUPROFEN; ADVAIR; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; FLONASE [FLUTICASONE PROPIONATE]; NORA-BE

Current Illness:

ID: 1000009
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Sore arm; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender received the second dose of 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 medical history and concomitant medications were not reported. The patient experienced sore arm on an unspecified date. Outcome of the event was unknown. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000010
Sex: F
Age:
State: NC

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

Lab Data:

Allergies:

Symptoms: her hands were cold; Her hand went numb/ feels the tingling/numbness for the most part from the wrist down; her left hand has been tingly/ Her hand tingling started almost immediately after getting the vaccine/ feels the tingling/numbness for the most part from the wrist down; This is a spontaneous report from a contactable consumer (patient [dental hygienist]). A 39-year-old female patient received first single dose of BNT162B2 (Pfizer, Solution for injection, lot number: EL3247, exp date not reported), via an unspecified route of administration (injection in left upper arm) from 15Jan2021 13:15 as COVID Vaccine. Vaccination Facility Type: Clinic. Medical history included hands were sometimes cold. Concomitant medication included cyanocobalamin (VITAMIN B12) given as self-injections in upper leg once a week on Sundays. The patient was previously given seasonal flu vaccine on Oct2020. No prior vaccinations within 4 weeks. Patient received her first dose of the COVID Vaccine today around 1:15PM or so the day of reporting and almost immediately started to experience event: She drove off from the waiting area; he was taking pictures; she commented her hands were cold, but her hands were sometimes cold anyway. She received the injection in her left upper arm. Since getting the injection in her left upper arm her left hand has been tingly. It was like it was asleep. She was wondering if they possibly hit a nerve or something when administering. She has called her doctor as well. Her hand tingling started almost immediately after getting the vaccine. She had to wait 15 minutes to be observed if any symptoms occurred. She waited, took selfies and also mentioned she contacted her doctor she works with. Her hand went numb and cold. She thought it was weird. At first, she thought it was just like her hand getting cold, but it never went away. She still feels it and it is like hand went asleep like if lay on it too long. She added she has on a watch and that was around the area where she feels the numbness so during the call she took it off. She feels the tingling/numbness for the most part from the wrist down, but she also feels it higher up as well, but mainly from the wrist down. She was hoping that does not happen where she has to go. She has called the doctor already and was advised what to do. No emergency room visit/ physician office visit was made for the events. Outcome of hand tingly was not recovered (ongoing at the time of reporting) and unknown for the other events.

Other Meds: VITAMIN B12 [CYANOCOBALAMIN]

Current Illness:

ID: 1000011
Sex: F
Age:
State: MI

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

Lab Data:

Allergies:

Symptoms: Hives on back, arm, knee, toe and hands; Itching on different parts of body; This is a spontaneous report from a contactable consumer, the patient. A 25-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number EL3248), via intramuscular route of administration on 13Jan2021 at 13:35 (at the age of 25-years-old) as a single dose in the right arm for COVID-19 vaccination. Medical history included asthma that is fairly mild (the patient has rescue inhaler that she does not use very often, she uses it once every few months as needed. Diagnosed in early childhood when she was 4-5 years old). The patient had no relevant family medical history. Concomitant medications included an unspecified medication, the patient reported she has been taking it for years, but did not provide further information. Historical vaccine included flu shot in Nov2020, which was greater than 4 weeks prior to receiving the COVID-19 vaccination. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 13Jan2021 at 15:00-16:00, the patient experienced itching on different parts of body. On 14Jan2021 at 10:00, the patient experienced hives on back, arm, knee, toe and hands. The reported clinical course was as follows: Initially, on the first day, she had itching not at injection site. It was on different parts of her body. The following day, she developed hives on her back, arm, knee, toe and hands. The patient reported it is not very severe, she did not have any fever, swelling, or shortness of breath. The patient reported some of the areas have gone down and some have inflamed more. The patient did not undergo any relevant test and reported just visual examination. The patient went to urgent care (physician office) and they said it was potentially caused by the COVID-19 vaccination. The patient was prescribed steroids by the urgent care as treatment for the events. The patient received one steroid injection of Methyl Prednisone into her buttocks and then was prescribed prednisone 10 mg tablets. The clinical outcomes of the itching on different parts of body and hives on back, arm, knee, toe and hands were not recovered. The patient was inquiring if she should get the second dose.

Other Meds:

Current Illness:

ID: 1000012
Sex: F
Age:
State:

Vax Date: 12/31/2020
Onset Date: 01/01/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: tested positive; Test Result: Positive

Allergies:

Symptoms: The patient received the vaccine on 31Dec2020 and then tested positive a week later; The patient received the vaccine on 31Dec2020 and then tested positive a week later; This is a spontaneous report from a contactable other HCP (healthcare professional) via a Pfizer-Sponsored Program,. A 41 (units not provided) female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; solution for injection) via an unspecified route of administration on 31Dec2020 (at an unspecified age) as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. It was reported that the patient received the vaccine on 31Dec2020 and then tested positive a week later. The patient stated that she was supposed to receive the vaccine this Thursday and she wanted to know if she could receive the vaccine. The clinical outcome of the event "the patient received the vaccine on 31Dec2020 and then tested positive a week later" 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 information currently available, lack of efficacy of the suspected vaccine BNT162B2 cannot be completely excluded. However, individuals may not be protected until at least 7 days after their second dose of the vaccine. It is unlikely that the patient would have fully developed immunity due to the very short time lag between the first vaccine dose and the event onset.

Other Meds:

Current Illness:

ID: 1000013
Sex: M
Age:
State:

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

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

Allergies:

Symptoms: got tested and tested positive; Got tested and tested positive; lethargic; This is a spontaneous report from a contactable consumer. This consumer reported similar events for two patients (husband and wife). This is the second of two reports (for the husband). A 74-year-old male patient received the first dose of BNT162B2 (Pfizer-BIONTECH Covid-19 Vaccine; lot number and expiry date were not reported), via an unspecified route of administration on 04Jan2021 as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, reported as two days after, the patient was lethargic. A week ago on an unspecified date, reported as past Monday, the patient had no cough, no fever, received azithromycin, got tested and tested positive. The patient underwent laboratory tests and procedures which included COVID-19 test: positive on an unspecified date. Outcome of the events was unknown. No follow-up attempts are possible. Information about the lot/batch cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021034433 same reporter, same drug/event, different patient

Other Meds:

Current Illness:

ID: 1000014
Sex: M
Age:
State:

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

Lab Data: Test Name: blood pressure; Result Unstructured Data: Test Result:went up for a day or two; Comments: BP was already going up as he keeps track of it

Allergies:

Symptoms: This is a spontaneous report received from a non-contactable consumer via a Pfizer-sponsored program. A male patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), via an unspecified route of administration, on an unspecified date, at single dose, for COVID-19 immunization. Medical history included ongoing blood pressure (BP) increase (BP was already going up). The patient's concomitant medications were not reported. It was reported that the patient received first dose of COVID vaccine and then his blood pressure went up for a day or two on an unspecified date. The patient's BP was already going up as he keeps track of it and thinks it's a coincidence but was just checking if this can happen. The outcome of the event was unknown. No follow-up attempts are Possible. Information on lot/batch cannot be obtained.

Other Meds:

Current Illness: Blood pressure increased

ID: 1000015
Sex: F
Age:
State:

Vax Date: 12/28/2020
Onset Date: 01/04/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210104; Test Name: test; Test Result: Positive

Allergies:

Symptoms: Caller got first vaccine dec 28th, tested positive jan 4th; Caller got first vaccine dec 28th, tested positive jan 4th; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer reported that a female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiration date not provided), via an unspecified route of administration on 28Dec2020 at Single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient got first vaccine on 28Dec2020, tested positive 04Jan2021. The patient wanted to know if she needed to wait to get second dose or if she should wait. The outcome of the event was unknown. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000016
Sex: F
Age:
State: MI

Vax Date: 01/08/2021
Onset Date: 01/10/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Left eye ball/socket soreness when moving side to side, up and down; Sinus pressure left eye; This is a spontaneous report from a contactable other hcp. A 42-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), (lot number: El3248), intramuscular, in the left arm, on 08Jan2021 16:45 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient received the first dose of BNT162B2 on an unspecified date for COVID-19 immunization. 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. Since the vaccination, the patient hasn't been tested for COVID-19. The patient experienced "left eye ball/socket soreness when moving side to side, up and down" and sinus pressure left eye on 10Jan2021 10:00. the outcome of events was recovering. Therapeutic measure taken as a result events included Sufdafed. No follow-up attempts are possible. No further information is expected. Information on the lot/batch number has been obtained.

Other Meds:

Current Illness:

ID: 1000017
Sex: F
Age:
State:

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

Lab Data: Test Name: Covid test; Test Result: Negative ; Comments: but throughout the weeks of quarantine, I've tested about every 4 days and consistently have been negative

Allergies:

Symptoms: I'm happy to say I got the second dose and had no side effects other than a sore arm.; This is a spontaneous report received from a contactable Nurse (patient). A female patient of unspecified age received dose 2 of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and Expiration date was unspecified) on unspecified date as single dose for COVID-19 immunisation. Medical history included being immunosuppressed. Historical vaccine included first dose of BNT162B2. Concomitant medication was not reported. The patient reported 'I'm happy to say I got the second dose and had no side effects other than a sore arm' on unspecified date. A week after getting the first shot, my daughter got Covid. My son and husband were positive shortly after her. I did get some very mild symptoms, but throughout the weeks of quarantine, I've tested about every 4 days and consistently have been negative. Lab data included Covid test which was negative on unspecified date ('but throughout the weeks of quarantine, I've tested about every 4 days and consistently have been negative'). Outcome of event sore arm was unknown. The lot number for the vaccine BNT162B2 was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1000018
Sex: F
Age:
State: OR

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

Lab Data:

Allergies:

Symptoms: Very sore arm; Headache; Very tired; This is a spontaneous report from a contactable healthcare professional (reporting for herself). A non-pregnant 38-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), intramuscularly in the left arm on 16Jan2021 05:45 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced very sore arm, headache and very tired in Jan2021. The outcome of the events was unknown. No follow-up attempts are possible; information about batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1000019
Sex: F
Age:
State: LA

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

Lab Data:

Allergies:

Symptoms: Itching/She was itching on her knee, leg, arm, neck, and ears.; She had hives on the knee; The two that had her most worried was the memory loss and chest pain; Chest pain; It was like she went blank. She was looking around and she could not remember names she was trying to figure out name street; Spasms/spasms were like in her back where her shoulders were and it was bulging; It hurt from her neck and up into her head.; It hurt from her neck and up into her head.; This is a spontaneous report from a contactable consumer (patient). A 77-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot EL3246, expiration date unspecified), via an unspecified route of administration on 10Jan2021 (around noon) at single dose (left arm) for COVID-19 immunization. Medical history included ongoing diabetes, ongoing blood pressure high/blood pressure, ongoing heart problems; heart disease, kidney disease, history of itching, fluid (imbalance), stroke so taking for clotting, history of neck issues and she was allergic to a lot of medications. Ongoing concomitant medications included ubidecarenone (COQ-10), zinc, torsemide for fluid, clopidogrel for had a stroke so taking for clotting, insulin glargine (LANTUS) for diabetes and isosorbide mononitrate, carvedilol, irbesartan and amlodipine, all for blood pressure. Patient reported that she got the injection on Sunday and then later she started to get spasms on 12Jan2021. These spasms were like in her back where her shoulders were and it was bulging and it hurt from her neck and up into her head. She mentioned she was 77 years old and sometimes she has to think about a word before she gets it out, but yesterday (14Jan2021) it was different. It was like she went blank. She was looking around and she could not remember names she was trying to figure out name street on and this lasted 15 minutes and then it went away. She confirmed she does not have it right now. It did not last a long time, but it scared her so bad. Then yesterday evening (14Jan2021), she started to have funny chest pain. She told her husband if it did not go away she would go to the ER. However, after an 1 hour it went away. It was like a sticking pain. The chest pain lasted for an hour and started around 18:00. On an unspecified date, she started itching at night. She has a history of itching, but this was out the box. She had hives on the knee. It was crazy. She itched all over. She had to get out of bed and sit in a chair until 1:30AM. She was still itching, but it was not as bad. Patient reported that due to the kidney disease she has itching, but the itching she was having after this COVID Vaccine was different and more. It was out of the box. She confirmed this was the first injection and now she was scared to get the second injection. Patient reported that the itching started when she went to bed. She went to bed around 21:00 and around 21:30, she got out of bed because she was itching so bad. She stated there was not anything different on the bed. It was the same thing that was up there the night before. She did not change the sheets or anything. She had to get up and sit in a chair and she could not believe how bad her knee was itching. She was itching on her knee, leg, arm, neck, and ears. She stated she takes a lot of medications. She was very funny with medications and they have to work with her to get the right one for her. Due to having these other conditions was why she wanted to get the COVID Vaccine. She reported she will have her blood drawn next week. The two that had her most worried was the memory loss and chest pain. However, these passed and she did not go the ER or physician office. She was afraid if she gets the second injection this will happen again and she may not come out as well form it. Prior vaccinations within 4 weeks was none. Outcome of events spasms/spasms were like in her back where her shoulders were and it was bulging and itching/itching on her knee, leg, arm, neck, and ears was recovering; chest pain was recovered on 14Jan2021 at 19:00; and outcome of the rest of events was unknown.

Other Meds: COQ-10; ZINC; TORSEMIDE; ISOSORBIDE MONONITRATE; CLOPIDOGREL; CARVEDILOL; IRBESARTAN; AMLODIPINE; LANTUS

Current Illness: Blood pressure high; Diabetes; Heart disorder

ID: 1000020
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: slight tenderness at injection site; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age (age:78; unit: unknown) started to receive 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. Patient is scheduled 4 weeks out for second dose of Covid Vaccine and wanted to know if thats okay. She experienced a slight tenderness at injection site. The patient and her husband received the vaccine. They scheduled the 2nd dose in 4 weeks instead of 3 weeks, they were asking if it was ok. They went to the clinic. It was very well organized. She asked if the next appointment going to be 3 weeks where they administered the vaccine. They were told that they are getting the Pfizer one and it's going to be 4 weeks. Then they waited for 15 minutes and went to the open computers for scheduling of the 2nd shot. The next shot is scheduled for 15Feb or 16Feb whichever one is a Wednesday works better for them. This morning her husband was reading the newspaper and it stated it cannot be given more than 23 days, this is going to be 32 days. They asked if they can reschedule. They will call the hospital or maybe change their appointment using the website/app. They were asking what is the timing of the 2nd dose of vaccine. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000021
Sex: F
Age:
State: MA

Vax Date: 12/28/2020
Onset Date: 01/04/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210104; Test Name: COVID-19 virus test; Result Unstructured Data: Test Result:Positive

Allergies:

Symptoms: She tested positive for Covid; She tested positive for Covid; This is a spontaneous report from a contactable nurse. A 62-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Solution for injection, lot number: EJ1686), via an unspecified route of administration from 28Dec2020 to 28Dec2020 at SINGLE DOSE for COVID-19 immunisation. Medical history was not reported. There were no concomitant medications. The nurse that stated that the patient got the first Covid-19 injection on the 28Dec2020 and reported that on the 04Jan2021, she tested positive for Covid. She said that she has been quarantining and was totally asymptomatic. She said that she is due to get the second vaccine on 18Jan2021. The outcome of the events was unknown.; Sender's Comments: Based on the information provided, the lack of efficacy cannot be excluded for vaccine BNT162B2 .

Other Meds:

Current Illness:

ID: 1000022
Sex: F
Age:
State: PA

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

Lab Data:

Allergies:

Symptoms: hive in the middle of her chest, it is swollen and raised; This is a spontaneous report from a contactable consumer (patient). A 67-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9231), via an unspecified route of administration (left upper arm) on 14Jan2021 (15:30) at single dose for Covid-19 immunization. The patient's medical history included blood cholesterol abnormal, anxiety, high blood pressure, sleep disorder, and obesity. Concomitant medication included amlodipine besilate (NORVASC) for high blood pressure been on it for years and ongoing, hydroxyzine for anxiety been on this medication for 10 years and ongoing, trazodone for sleep taking for 10 years and ongoing, pravastatin sodium (PRAVACHOL) for cholesterol taking for 12 years and ongoing, and colecalciferol (VITAMIN D) from 2019 and ongoing. In November, she received her shingle shot and croup shot. The patient reported that got she the vaccine yesterday (14Jan2021S). She woke up with a hive on 15Jan2021 (8:30 am). She has a hive in the middle of her chest, it is in between her boobs. She added that it is swollen. There is nothing else anywhere. She is going to take Benadryl. She didn't have a prescribing doctor. Her boss set up the appointment for them. The hive has stayed, it is swollen and raised. Her second dose is scheduled on 04Feb2021. The outcome of event was not recovered.

Other Meds: NORVASC; HYDROXYZINE; TRAZODONE; PRAVACHOL; VITAMIN D [COLECALCIFEROL]

Current Illness:

ID: 1000023
Sex: M
Age:
State: KY

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

Lab Data: Test Date: 202101; Test Name: blood tests; Result Unstructured Data: Test Result:normal (some two blood tests/normal); Test Date: 202101; Test Name: chest x-ray; Result Unstructured Data: Test Result:normal; Test Date: 202101; Test Name: EKG; Result Unstructured Data: Test Result:normal

Allergies:

Symptoms: slight heart palpitations like quivering which went on for 18 hours; This is a spontaneous report from a contactable healthcare professional (patient). A 72-year-old male patient received first dose of (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, lot number: 5/31 EL 3249 (as reported), unknown expiration), via an unspecified route of administration in right arm on 13Jan2021 at 14:00 (02:00 PM) at a single dose for COVID-19 immunization in a hospital. Medical history included known allergies to shellfish. Concomitant medications included enalapril, metformin, insulin, and clopidogrel. Four hours later that evening of 13Jan2021 at 06:30 PM (18:30), the patient experienced slight heart palpitations like quivering which went on for 18 hours. He went to a hospital for 3 hours EKG, chest x-ray, and some two blood tests, all of which came back normal (Jan2021). He had no issues like this before or since. The event resulted in emergency room/department or urgent care visit. The patient has no COVID prior to vaccination and was not tested for COVID post vaccination. The patient did not receive other vaccine in four weeks. The patient did not receive treatment for the event. The patient recovered from the event in Jan2021.

Other Meds: ENALAPRIL; METFORMIN; INSULIN; CLOPIDOGREL

Current Illness:

ID: 1000024
Sex: M
Age:
State: CA

Vax Date: 01/16/2021
Onset Date: 01/19/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: anxious; cognition has degraded; wounded; his confusion was the worst I've ever seen. He was totally inattentive; totally inattentive; This is a spontaneous report from a contactable consumer (patient's daughter). A 93-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EJ1686) via an unspecified route of administration on the left arm on 16Jan2021 12:30 at a single dose for COVID-19 immunization. Medical history included type 2 diabetes, CHF, impaired kidney function, atrial fibrillation, multiple strokes, dementia/memory issues, confusion. Concomitant medications were not reported (unspecified 15 meds). The patient previously took blood thinners. It was reported that the patient suffered from memory loss and dementia, and on 19Jan2021 his confusion was the worst the reporter had ever seen. He was totally inattentive - like, he kept tuning out until she said, Dad, Dad. Then he'd listen and it was as if he couldn't remember the sentence from 2 minutes ago. He was having difficulty putting together a coherent thought. He was not in any pain. The patient still functioned well. She said since receiving the 1st dose of the vaccine, she noticed that her dad's cognition has degraded in a very concerning way. He was very confused and anxious. She said this was all new behavior, and just started to happen after her dad received the vaccine. Then last night on 19Jan2021, apparently he wandered, which he never does, and he tried to push a nurse or aide, and tried to go into a neighbor's room, a friend, so he was looking for a safe place, and he was hitting a doorknob, and he is on a blood thinner, so he wounded himself and bled, he is on blood thinners, he didn't bleed out, she wrapped his wrist and it's fine. No treatment was received for the events 'his confusion was the worst I've ever seen. He was totally inattentive'. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The facility where the vaccine was administered was in a facility. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient has not been tested for COVID-19. No known allergies. Outcome of the event 'his confusion was the worst I've ever seen. He was totally inattentive' was not recovered while unknown for the other events.

Other Meds:

Current Illness:

ID: 1000025
Sex: F
Age:
State: TX

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

Lab Data:

Allergies:

Symptoms: arm has been sore; looked like she had a sunburn all over her body/sunburn looking skin felt like her skin was on fire and her clothes itched, they felt like she had sandpaper on; looked like she had a sunburn all over her body/sunburn looking skin felt like her skin was on fire and her clothes itched, they felt like she had sandpaper on; looked like she had a sunburn all over her body/sunburn looking skin felt like her skin was on fire and her clothes itched, they felt like she had sandpaper on; looked like she had a sunburn all over her body/sunburn looking skin felt like her skin was on fire and her clothes itched, they felt like she had sandpaper on; This is a spontaneous report from a contactable consumer (patient). A 70-year-old female patient received first single dose of BNT162B2 (Solution for injection, batch/lot number and exp date not reported), via an unspecified route of administration (Vaccination site: left, almost her shoulder) on 14Jan2021 13:45 as COVID vaccine. The vaccine was administered at clinic. Vaccine not administered at military facility. There were no concomitant medications. Patient had no prior Vaccinations (within 4 weeks). The patient previously took acetylsalicylic acid (ASPIRIN), ibuprofen and NSAIDS wherein she was allergic. This was years and years ago. When she took the products, she had silver dollar size hives from head to toe. Patient asked if there was any of this in the vaccine. The patient previously got shingles vaccine on 2019 (2 years ago) at the pharmacy wherein she had a sore arm and a bruise. The patient had no other relevant history. Patient reported she just got home from the emergency room. It was explained that on 14Jan2021 (yesterday) she got the vaccine. On 15Jan2021, her arm had been sore today since getting up but about 1pm today she looked like she had a sunburn all over her body. Her husband gave her 2 diphenhydramine (BENADRYL) and rushed her to the emergency room. They told her that they can't say for sure but that was likely that it was caused by the vaccine. The soreness was about the same. Looking like she had a sunburn all over her body, that was gone. The patient further explained the sunburn looking skin felt like her skin was on fire and her clothes itched, they felt like she had sandpaper on. There have been no other treatments. She remarks she had to wait so long in the emergency room by the time they saw her it had resolved. Investigation assessment/relevant tests were not performed. The emergency room told her the Benadryl likely knocked it out. They offered Tylenol and an IV but she declined; she felt there was no reason since she was doing better. She was told to take 2 more diphenhydramine 25mg in 6 hours. No physician office visit required for the events. She was supposed to get the second dose on 04Feb2021 but was told to ask if she should still get it. The outcome of arm has been sore was not recovered, while other events recovered on 15Jan2021. Information about lot number and expiry date for the suspect product will be requested in follow-up attempts.

Other Meds:

Current Illness:

ID: 1000026
Sex: M
Age:
State: MO

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

Lab Data: Test Date: 20201201; Test Name: Salivary Sample; Test Result: Negative

Allergies:

Symptoms: Chill like sensations; Aches; Dyspnea on Exertion; General Malaise; Fever; Persistent headache that is not relieved with pain killers; other vaccine same date vaccine date 22Dec2020, dose number 1; other vaccine same date vaccine date 22Dec2020, dose number 1; This is a spontaneous report from a contactable consumer. A 40-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899, expiry date not reported), intramuscular in the right arm on 22Dec2020 07:30 at single dose for COVID-19 immunisation. Medical history was none. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was vaccinated at a hospital. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient has been tested for COVID-19. The patient had no allergies to medications, food, or other products. Concomitant medications included amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL XR), amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL IR), vitamin d3, calcium ascorbate (VITAMIN C), vitamin b complex, magnesium, cynara cardunculus extract (ARTICHOKE EXTRACT), and vaccinium macrocarpon (CRANBERRY EXTRACT). On 23Dec2020 07:00, the patient experienced chill like sensations, aches, dyspnea on exertion, general malaise, fever, persistent headache that is not relieved with pain killers. It was also reported that other vaccine with same date vaccine date on 22Dec2020, dose number 1. The patient underwent lab tests and procedures which included salivary sample (SARS-cov-2 test): negative on 01Dec2020 . No treatment was received for the adverse events. Clinical outcome of the events was recovered on an unspecified date.

Other Meds: ADDERALL XR; ADDERALL IR; VITAMIN D3; VITAMIN C; VITAMIN B COMPLEX; MAGNESIUM; ARTICHOKE EXTRACT; CRANBERRY EXTRACT

Current Illness:

ID: 1000027
Sex: F
Age:
State: IN

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

Lab Data:

Allergies:

Symptoms: Coughing; Jaw pain; Fatigue the same day as vaccine; This is a spontaneous report from a non-contactable other healthcare professional (HCP; patient herself). A 29-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot/batch number and expiration date were unknown), intramuscularly on the right arm on 18Jan2021 at 10:45 at a single dose for COVID-19 immunization. The facility where the most recent COVID-19 vaccine was administered was at the hospital. The patient's medical history was not reported; she had no allergies to medications, food, or other products. Concomitant medications included dexamethasone, bupropion, and hydroxyzine hydrochloride (HYDROXIZINE). 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 patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient experienced fatigue the same day as vaccine on 18Jan2021 at 13:00. Two days later, on 20Jan2021, the patient experienced coughing and jaw pain. The reporter assessed the events as non-serious. The patient did not receive any treatment for the adverse events. The patient was recovering from all the events. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds: DEXAMETHASONE; BUPROPION; HYDROXIZINE

Current Illness:

ID: 1000028
Sex: F
Age:
State: NC

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

Lab Data:

Allergies:

Symptoms: Swelling, redness, irritation, itching, a visible bump approximately the size of a quarter on the arm and irritation site is the size of a 1/2 dollar; Swelling, redness, irritation, itching, a visible bump approximately the size of a quarter on the arm and irritation site is the size of a 1/2 dollar; Swelling, redness, irritation, itching, a visible bump approximately the size of a quarter on the arm and irritation site is the size of a 1/2 dollar; Swelling, redness, irritation, itching, a visible bump approximately the size of a quarter on the arm and irritation site is the size of a 1/2 dollar; Swelling, redness, irritation, itching, a visible bump approximately the size of a quarter on the arm and irritation site is the size of a 1/2 dollar; This is a spontaneous report from a contactable other healthcare professional, the patient. A 51-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number: EL3249), via an unspecified route of administration in the left arm on 07Jan2021 at 15:45 (at the age of 51-years-old) as a single dose, for COVID-19 vaccination. There was no medical history. The patient was not pregnant at the time of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications were unknown. There were no allergies to medications, food, or other products. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 07Jan2021 at 10:00 PM, the patient experienced swelling, redness, irritation, itching, a visible bump approximately the size of a quarter on the arm and irritation site is the size of a 1/2 dollar. The events were reported as non-serious and continued 2 weeks after the first injection. The patient did not receive any treatment for the events. The clinical outcome of swelling, redness, irritation, itching, a visible bump approximately the size of a quarter on the arm and irritation site is the size of a 1/2 dollar were recovered with lasting effects. It was also reported that since the vaccination, the patient had not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1000029
Sex: F
Age:
State:

Vax Date: 01/11/2021
Onset Date: 01/13/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: nausea and dizziness/dizziness and nausea went pretty extreme; nausea and dizziness/dizziness and nausea went pretty extreme; This is a spontaneous report from a contactable consumer (husband of patient). A 60-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number, expiration date unspecified), via an unspecified route of administration on 11Jan2021 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On 13Jan2021, 2 days after vaccination, patient experienced nausea and dizziness, that went away. Until yesterday, 19Jan2021, her dizziness and nausea went pretty extreme. She was scheduled for a second dose in about 2 weeks, on 09Feb2021. Outcome of events was not recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000030
Sex: F
Age:
State: TX

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

Lab Data: Test Date: 20210118; Test Name: Fever; Result Unstructured Data: Test Result:99 or above

Allergies:

Symptoms: Fever 99 or above; Muscle pain; This is a spontaneous report from a contactable healthcare professional (patient). A 44-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot: el3249, expiry: unknown), via an unspecified route of administration on the left arm on 18Jan2021 06:00 at a single dose for COVID-19 immunization at a hospital. Medical history included hyper thyroid, type 1 diabetic and fatty liver. The patient has no known allergies. Concomitant medications included insulin glargine (LANTUS) and insulin lispro (HUMALOG). The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot: ej1685, expiry: unknown) on 30Dec2020 at 16:30 in the left arm for COVID-19 immunization. The patient experienced fever 99 or above and muscle pain on 18Jan2021 19:00. The events were not treated. The patient was not tested for Covid post vaccination. The outcome of the events was recovered on an unspecified date.

Other Meds: LANTUS; HUMALOG

Current Illness:

ID: 1000031
Sex: F
Age:
State:

Vax Date: 12/22/2020
Onset Date: 12/26/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20201226; Test Name: Covid-19 test; Test Result: Positive

Allergies:

Symptoms: developed pneumonia; tested positive for Covid-19; tested positive for Covid-19; This is a spontaneous report from contactable nurse, the patient. A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN), via an unspecified route of administration on 22Dec2020 as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On 26Dec2020, the patient tested positive for COVID-19 and subsequently developed pneumonia on an unknown date. Due to this, the patient did not get her second dose which was scheduled on 12Jan2021 as she was still ill. The clinical outcomes of COVID-19 and subsequently developed pneumonia were unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.; Sender's Comments: Based on the information currently available, lack of efficacy of the suspected vaccine BNT162B2 cannot be completely excluded. However, individuals may not be protected until at least 7 days after their second dose of the vaccine. It is unlikely that the patient would have fully developed immunity due to the very short time lag between the first vaccine dose and the event onset.

Other Meds:

Current Illness:

ID: 1000032
Sex: F
Age:
State: MI

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

Lab Data: Test Date: 20210120; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: Site pain; Headache; Nauseous; Cough; Felt congested; No taste or smell; No taste or smell; This is a spontaneous report from a contactable consumer (patient). A 48-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EF9231; Expiration date was not reported) on 11Jan2021 (09:30) at a single dose on the left arm, with route of administration unspecified, for COVID-19 immunization at the hospital. Medical history included breast cancer and hypertension. The patient's concomitant medications were not reported. On 18Jan2021, the patient had site pain; headache; and was nauseous. On 13Jan2021, the patient had cough. In Jan2021, after the vaccination, the patient had felt congested. In Jan2021, almost two weeks after the vaccination, the patient had no taste or smell. The reported events had resulted in the emergency room/department or urgent care. The outcome of the events, 'site pain', 'headache', 'nauseous', 'cough', 'felt congested' and 'had no taste or smell', was unknown. The patient was not diagnosed with COVID-19 prior to vaccination. On 20Jan2021, the patient had a nasal swab COVID-19 test, and was negative.

Other Meds:

Current Illness:

ID: 1000033
Sex: F
Age:
State: FL

Vax Date: 01/16/2021
Onset Date: 01/18/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: nasal congestion; headache; This is a spontaneous report from a contactable consumer (patient). This 73-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1283 and expiry date unknown), via an unspecified route of administration on 16Jan2021 20:15 at a single dose on the right arm for COVID-19 immunization. Medical history included high blood pressure, NTM lung infection, and laryngopharyngeal reflux (LPR). Concomitant medications included amlodipine, HCTZ, potassium bicarbonate, sodium alginate (GAVISCON ADVANCE), and telmisartan. The patient has no known allergies. Patient is not pregnant. The patient did not receive other vaccine in four weeks. The patient had no COVID-19 prior to vaccination. The patient has not been tested for COVID-19 post vaccination. On 18Jan2021, the patient experienced nasal congestion and headache. No treatment was received. Outcome of the events was recovering.

Other Meds: AMLODIPINE; HCTZ; GAVISCON ADVANCE [POTASSIUM BICARBONATE;SODIUM ALGINATE]; TELMISARTAN

Current Illness:

ID: 1000034
Sex: F
Age:
State: AZ

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

Lab Data: Test Name: fever; Result Unstructured Data: Test Result:100 degrees; Test Name: tested; Test Result: Positive ; Comments: before taking the vaccine

Allergies:

Symptoms: Runny nose; fever of 100 degrees; Chills; sore throat; congestion; This is a spontaneous report from a Pfizer-sponsored program from a contactable consumer (patient). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiration date not provided), 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 caller mentioned after taking the first shot, she had a runny nose, fever of 100 degrees, chills, congestion, sore throat. Wanting to know if it's possible that she was tested positive before taking the vaccine. The outcome of the events was unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1000035
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: Pain in left arm and at injection site; Pain in left arm and at injection site; Large bruise; This is a spontaneous report from a contactable consumer (patient herself). A 74-year-old female patient received BTN162B2 PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number: E13246, expiration date was unknown), via an unspecified route of administration on the left arm on 13Jan2021 at a single dose for COVID-19 immunization. The facility where the most recent COVID-19 vaccine was administered was at the public health clinic/veterans administration facility. Relevant medical history included allergies to Penicillin. The patient's concomitant medications were not reported. 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 patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 13Jan2021, the patient experienced pain in left arm and at injection site and large bruise, which were assessed as non-serious. One week after the injection, she still had pain in left arm and at injection site and also a large bruise. The patient did not receive any treatment for the adverse events. The patient was not recovered from all the events.

Other Meds:

Current Illness:

ID: 1000036
Sex: M
Age:
State: NY

Vax Date: 12/18/2020
Onset Date: 01/05/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data: Test Date: 20210105; Test Name: Sars-Cov-2 infection; Test Result: Positive

Allergies:

Symptoms: tested positive for a Sars-Cov-2 infection; tested positive for a Sars-Cov-2 infection; This is a spontaneous report from a contactable consumer (patient). This 38-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number EK5730) intramuscular in the left deltoid on 18Dec2020 at the age of 38-years-old at single dose for COVID-19 immunisation. There were no relevant medical history and concomitant medications. On 05Jan2021, the patient tested positive for a SARS-COV-2 infection. The patient was asking how to proceed with getting his second dose; at the time of the report, he was 2 weeks post diagnosis and he was 32 days since his first shot. At the time of the report, the outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1000037
Sex: M
Age:
State:

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

Lab Data: Test Name: Heart rate; Result Unstructured Data: Test Result:increased

Allergies:

Symptoms: elevated heart rate and heart palpitations; elevated heart rate and heart palpitations; This is a spontaneous report from a contactable healthcare professional (patient). A male patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiration date unspecified), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. Medical history included Covid-19 and recovered. The patient's concomitant medications were not reported. On an unspecified date, the patient experienced elevated heart rate and heart palpitations. It was reported that the patient received his 1st dose about 3 weeks ago shortly after he recovered from Covid-19. Patient was asking if he should receive second dose right away or if there was any data on possible exacerbated side effects with patients who recently recovered from COVID-19 before the vaccine. Outcome of events was unknown. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1000038
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: I feel pain in my LEFT arm, it feels like I've been punched on it; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age (Age: 84, unit: Unknown) received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number, expiration date unspecified), via an unspecified route of administration on 15Jan2021 at single dose (right arm) for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that she took the vaccine on 15Jan2021 and did it in her right arm, but she felt pain in her left arm on an unspecified date and it felt like she had been punched on it. Her second dose was scheduled on 05Feb2021. Outcome of the event was unknown. Information on the Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 1000039
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: My arthritis pain is gone; vivid dreams; This is a spontaneous report from a contactable consumer. A 64-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot: EL3246), via an unspecified route of administration on 12Jan2021 09:00 at a single dose for covid-19 immunization. The patient's medical history included allergy to IVP DYE, and osteoporosis from an unknown date. Concomitant medication included alendronate sodium (ALENDRONATE). The patient previously took varicella zoster vaccine (shingles vaccine on 03Dec2020), and povidone in generic tablets and experienced allergy. On 15Jan2021, the patient experienced her arthritis pain was gone. The patient also mentioned that she had vivid dreams in Jan2021 and haven't dreamed in years. The outcome of the event swas unknown. The patient did not received treatment for the event. The patient diagnosed with COVID-19 prior to vaccination and has not been tested for COVID-19 since the vaccination.

Other Meds: ALENDRONATE

Current Illness:

ID: 1000040
Sex: F
Age:
State:

Vax Date: 12/29/2020
Onset Date: 12/29/2020
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: a side effect that lasted a few minutes in her mouth an hour later from her first dose of the COVID-19 vaccine on 29Dec2020.; This is a spontaneous report from a non-contactable consumer (patient). A female patient of an unspecified age started received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on 29Dec2020 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced a side effect that lasted a few minutes in her mouth, an hour later from her first dose of the COVID-19 vaccine on 29Dec2020. The outcome of the event was recovered on unspecified date. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected

Other Meds:

Current Illness:

ID: 1000041
Sex: U
Age:
State:

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

Lab Data: Test Name: tested; Result Unstructured Data: Test Result:Positive

Allergies:

Symptoms: received the first dose of the COVID-19 vaccine on 22Dec2020/tested positive after taking the first dose; received the first dose of the COVID-19 vaccine on 22Dec2020/tested positive after taking the first dose; This is a spontaneous report from a contactable pharmacist. A patient of unspecified age and gender received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiration date not provided), via an unspecified route of administration on 22Dec2020 at SINGLE DOSE for COVID-19 immunisation. Patient's medical history and concomitant medications were not reported. It was reported that the pharmacist understood that the undiluted vials could be stored up to 120 hours in the refrigerator. She mentioned that their vials are already close to 120 hours stored in the refrigerator. She also knows that if you draw it up in a syringe, the vaccine has a 6-hr viability. She wanted to know if the vial expires after 120 hours or it would mean an additional 6 hours on top of the 120 hours. It was reported that "The allowable time in the refrigerator (5 days or 120 hours), starts when the vaccine is removed from storage under ultra-low temperatures. From the point of dilution, the vaccine may be stored at 2 degrees C to 30 degrees C for up to 6 hours." also shared extended stabiilty information of diluted vials". It was then reported that the patient received the first dose of the COVID-19 vaccine on 22Dec2020. However, the patient tested positive after taking the first dose. The pharmacist asked if the patient should be revaccinated with first dose and then wait for the another 2 weeks for the second dose. Pharmacist further asked if not, is it ok giving it at 8 days after the 21 day-interval, how to proceed, and dose the Regulatory recommendations included people who had COVID-19. Outcome of the event was unknown. Information on the lot/ batch number has been requested.; Sender's Comments: Based on available information, a possible contributory role of BNT162B2 cannot be completely excluded for reported "tested positive after taking the first dose".

Other Meds:

Current Illness:

ID: 1000042
Sex: M
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: muscle ache at the injection site; total body ache and soreness; headache; This is a spontaneous report from a contactable consumer (patient). This 59-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number EL1283) via an unspecified route of administration in the left arm on 19Jan2021 at 08:00 (at the age of 59-years-old) as a single dose for COVID-19 immunization. Medical history included a pacemaker, chronic obstructive pulmonary disease (COPD), asthma, and high blood pressure (HBP). Prior to the vaccination the patient was not diagnosed with COVID-19. The patient did not have any allergies. Concomitant medications included aspirin; lisinopril; fluticasone furoate, umeclidinium bromide, vilanterol (TRELEGY); and montelukast. The patient did not receive any other vaccines within 4 weeks prior to the vaccine. On 19Jan2021 at 11:00 the patient experienced muscle ache at the injection site, total body ache and soreness, and headache. The patient did not receive treatment for the events. The outcomes of injection site, total body ache and soreness, and headache were not recovered. It was also reported that since the vaccination the patient was not tested for COVID-19. No follow-up attempts are needed. No further information is expected.

Other Meds: ASPIRIN [ACETYLSALICYLIC ACID]; LISINOPRIL; MONTELUKAST; TRELEGY

Current Illness:

ID: 1000043
Sex: M
Age:
State: CT

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

Lab Data:

Allergies:

Symptoms: hack up from lungs to spit out and it was blood/spitting a blood about seven or eight times; This is a spontaneous report from a contactable consumer. An 89-year-old male patient received first dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine; lot/batch number and expiry date were unknown), via an unspecified route of administration in the arm on 14Jan2021 at a single dose for COVID-19 immunization. The patient's medical history was not reported. Concomitant medication included unspecified blood thinners. The consumer is a veteran and had the Pfizer COVID 19 vaccine first dose yesterday on 14Jan2021. He had it in his arm and got a print-out that he took out and it says something about if you have a bleeding disorder and are on blood thinners. His provider did not ask him. He wanted to know if this vaccine is a blood thinner. He felt good after getting it and went to sleep last night. He got up and sort of hack up from lungs to spit out and it was blood and was like that from 6am-7am on 15Jan2021. It was also reported that he was spitting a blood about seven or eight times but then it stopped. He is okay now. Nothing is happening. He wanted to know if he should take a blood thinner when he gets the second one. He would feel like he should not take the blood thinner when he gets the second one. The outcome of the event was recovered on 15Jan2021. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000044
Sex: M
Age:
State: OH

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

Lab Data:

Allergies:

Symptoms: out of the body experience as he has a sensation like he feels like a different person and sees everything different/feels weird; feels dizzy/has dizziness/when he sits, he feels like he was moving; vertigo; feels like he was drunk but was not drinking; overslept; This is a spontaneous report from a contactable consumer (patient). A 30-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number EL3249, expiry date 31May2021) via an unspecified route of administration (right arm), on 19Jan2021, at single dose, for covid-19 immunization. Medical history included Wolff-Parkinson-White syndrome from Nov2019 wherein the patient had surgery to correct. There were no concomitant medications. The patient just received the vaccine yesterday and wanted to report side effects. He stated he overslept this morning on 20Jan2021, and he was supposed to be at work at 7am. He rushed to get into his vehicle, and he was sitting at a stop light and started feeling this way at 8am. He stated that on 20Jan2021 08:00 he has an out of the body experience as he has a sensation like he feels like a different person and sees everything different. He feels dizzy/has dizziness kinda like vertigo on 20Jan2021 08:00. He added it feels like vertigo, but it was not vertigo, he was unsure if it was vertigo. Everything feels weird. He feels like he was drunk but was not drinking and, when he sits, he feels like he was moving on 20Jan2021 08:00. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1000045
Sex: M
Age:
State:

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

Lab Data: Test Date: 202101; Test Name: Covid; Test Result: Positive

Allergies:

Symptoms: tested positive for Covid after getting the first dose of vaccine; tested positive for Covid after getting the first dose of vaccine; This is a spontaneous report from a contactable consumer (patient). A 77-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot/batch number: not provided), via an unspecified route of on 16Jan2021 at SINGLE DOSE for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient had previously received the first dose of shingles shot as immunization on an unknown date. It was stated that the patient tested positive for COVID after getting the first dose of vaccine in Jan2021. The patient also mentioned that he was scheduled to have a second dose of PFIZER-BIONTECH COVID-19 VACCINE on 06Feb2021 and his second shot of shingles shot on 09Feb2021. Outcomes of the events were unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1000046
Sex: M
Age:
State: NJ

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

Lab Data:

Allergies:

Symptoms: I could not hear anything; This is a spontaneous report from a contactable consumer (patient). An 86-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: el8982), via an unspecified route of administration at the left arm on 18Jan2021 09:00 at a single dose for COVID-19 immunization. Medical history included hearing problem, CAD and glaucoma. The patient has no allergies to medications, food, or other products. Concomitant medication included tamsulosin, levothyroxine sodium (LEVOXYL), omeprazole, acetylsalicylic acid (BABY ASPIRIN) and astorta. On 19Jan2021, 1 day after injection around 5pm the patient reported to have taken a nap, and when he woke up, he could not hear anything. The patient has a hearing problem only have 10% hearing. He was going to see ENT. The event resulted to doctor or other healthcare professional office/clinic visit. The reporter assessed the event as non-serious, did not result in death, not life threatening, did not cause/prolonged hospitalization, not disabling/incapacitating, did not cause congenital anomaly/birth defect. The patient has not received any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient has not been tested for COVID-19 post vaccination. The outcome of the event was not recovered

Other Meds: TAMSULOSIN; LEVOXYL; OMEPRAZOLE; BABY ASPIRIN

Current Illness:

ID: 1000047
Sex: M
Age:
State: KS

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

Lab Data:

Allergies:

Symptoms: Lightheaded, dizzy for 4 hours; Toes, fingers and lips numb and tingly for 2 hours; Toes, fingers and lips numb and tingly for 2 hours; Toes, fingers and lips numb and tingly for 2 hours; Toes, fingers and lips numb and tingly for 2 hours; This is a spontaneous report received from a contactable physician (who is also the patient). A 56-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247, expiry date: unknown), via an unspecified route of administration in the left arm, on 19Jan2021 13:30, at single dose, for COVID-19 immunization, in the hospital. Medical history included asthma and environmental allergies. The patient did not have COVID-19 prior to vaccination and was not tested for COVID-19 post vaccination. The patient did not have other vaccine in four weeks. Concomitant medications were unspecified (had other unspecified medications in two weeks). Historical vaccine included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL0142, expiry date unknown), via an unspecified route of administration in the left arm, on 31Dec2020 13:30, for COVID-19 immunization. The patient was lightheaded, dizzy for 4 hours and experienced toes, fingers and lips numb and tingly for 2 hours, all on 19Jan2021 16:45. The events resulted in emergency room/department or urgent care visit. No treatment was provided. The patient recovered from dizzy for 4 hours on 19Jan2021 20:45 and from toes, fingers and lips numb and tingly for 2 hours on 19Jan2021 18:45.

Other Meds:

Current Illness:

ID: 1000048
Sex: F
Age:
State: NJ

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

Lab Data: Test Name: Body temperature; Result Unstructured Data: Test Result:95 degree

Allergies:

Symptoms: pounding headache; Chills; This is a spontaneous report from a contactable pharmacist (patient). A 34-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL8982), via an unspecified route of administration in left arm on 19Jan2021 13:45 at single dose for COVID-19 immunization. Medical history was reported as none. Concomitant medication included bifidobacterium lactis (PROBIOTIC), ascorbic acid (VIT C) and a multivitamins. The patient was not pregnant. The facility where the most recent COVID-19 vaccine was administered was in the Public Health Clinic facility. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, it was unknown if the patient was diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 20Jan2021 04:00 AM, the patient stated, "In the middle of the night after my vaccination, I had a pounding headache that is still ongoing as of 11:18 am eastern. I am also now experiencing chills for the last 2 hours (my current body temp is 95 degrees)". The outcome of the events was not recovered. No treatment was given to the patient for the events.

Other Meds: PROBIOTIC [BIFIDOBACTERIUM LACTIS]; VIT C

Current Illness:

ID: 1000049
Sex: M
Age:
State: LA

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

Lab Data:

Allergies:

Symptoms: diarrhea; This is a spontaneous report from a Pfizer sponsored program Pfizer First Connect. A contactable consumer reported that a male patient of an unspecified age received his first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 14Jan2021 at single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient stated after took the first shot last on 14Jan2021 he experienced little diarrhea in Jan2021. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1000050
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: severe platelet problem after receiving the vaccine; This is a spontaneous report from a contactable consumer. A patient (doctor) of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiry 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. On an unspecified date, the patient experienced a severe platelet problem after receiving the vaccine. The reporter was looking for information on patients with autoimmune diseases (specifically scleroderma and thrombocytopenia) who received the vaccine. The outcome of the event severe platelet problem was unknown. Information about Lot/Batch number is requested.

Other Meds:

Current Illness:

ID: 1000051
Sex: F
Age:
State: FL

Vax Date: 01/13/2021
Onset Date: 01/16/2021
Rec V Date: 02/04/2021
Hospital:

Lab Data:

Allergies:

Symptoms: bad chills/terrible chills; terrible acid reflux for 3 hours; couldn't even walk, she had to crawl and her husband had to walk her around, she couldn't do anything; threw up; very dizzy/dizziness; vertigo; This is a spontaneous report from a contactable consumer (patient). A 70-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL8982, unknown expiration), via injection in right arm on 13Jan2021 at a single dose for COVID-19 prevention. Medical history included ongoing vertigo (in car accident a little over 5 years ago, that affected a big nerve in left temple, and so every once in a while she will get vertigo so bad that she falls over), ongoing GERD (from a hiatal hernia; diagnosed many years ago), ongoing high blood pressure diagnosed about 15 years ago, ongoing bad cholesterol diagnosed 10 to 15 years ago, ongoing heart burn, ongoing hiatus hernia, and car accident a little over 5 years ago. Concomitant medications included ongoing omeprazole sodium (OMEPRAZOLE) for GERD, heart burn, and hiatal hernia (started this product at least 10 years ago; takes the product as needed if she is having heart burn or is going to eat spicy food); ongoing vitamin D3 for vitamin supplementation (started product about 8 months ago, because her doctor told her too, she guesses her vitamin was low); ongoing metoprolol for high blood pressure and to prevent stroke (started product at least 15 years ago; her BP could be regular but it could shoot up when she is upset, so she takes this to prevent stroke); ongoing hydrochlorothiazide for blood pressure (started product at least 5 years ago); pravastatin for bad cholesterol (started the product at least 4 or 5 or more years ago); and ongoing acetylsalicylic acid (BABY ASPIRIN) to prevent stroke (has been taking this product forever, at least for 10 years). The patient reported that she received the first COVID shot on 13Jan2021. She was okay on the 13th, 14th, and 15th. However, on the 16th (16Jan2021), she woke up and threw up once and was very dizzy for three days. She mentioned that she had like vertigo, she couldn't even walk, she had to crawl and her husband had to walk her around, she couldn't do anything. She had vertigo (16Jan2021). She was that way on Saturday and Sunday. On Monday, the patient's son took her to acupuncturist for her dizziness and was able to get up fine and walked away. After the acupuncture, she felt fine, like she was all better. On 19Jan2021 (reported as yesterday), she was fine. She woke up at midnight and had terrible acid reflux for 3 hours even though she had hardly eaten. She does take omeprazole for heart burn, and she had taken omeprazole earlier in the day, but it was just coming up, that acid and burning. She drank milk to coat the stomach and it went away at 03:00 AM. She had very bad chills/terrible chills (20Jan2021) and her teeth were chattering, she couldn't even talk, and couldn't control the chills. She is fine now. She clarified that she got vertigo from a car crash years ago and haven't had it in almost a year. Chills are not ongoing at this time, she has not had any for about 4 hours now, and she is hoping she is recovered completely, but it may be too soon to tell. She did not receive other vaccines on the same day as the COVID vaccine. The patient is wondering if all this could be from the vaccine. The patient wanted to know if it is safe to take the second shot. She was scheduled to receive the second dose on 03Feb2021. The patient recovered from the events threw up on 16Jan2021; unable to walk and vertigo on 18Jan2021; dizziness on 19Jan2021; and terrible acid reflux on 20Jan2021. While unknown outcome for chills.

Other Meds: OMEPRAZOLE [OMEPRAZOLE SODIUM]; VITAMIN D3; METOPROLOL; HYDROCHLOROTHIAZIDE; PRAVASTATIN; BABY ASPIRIN

Current Illness: Blood cholesterol abnormal (diagnosed 10 to 15 years ago.); Blood pressure high (diagnosed about 15 years ago); GERD (GERD from a Hiatal Hernia; diagnosed many years ago); Heartburn; Hiatal hernia; Vertigo (in car accident a little over 5 years ago, that affected a big nerve in left temple)

ID: 1000052
Sex: M
Age:
State: IL

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

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

Allergies:

Symptoms: he tested positive for COVID-19 between the 1st and 2nd dose of the vaccination schedule; he tested positive for COVID-19 between the 1st and 2nd dose of the vaccination schedule; Fever; This is a spontaneous report from a contactable consumer (patient's wife). A 76-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiry date unknown), intramuscular 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 tested positive for COVID-19 between the first and second dose of the vaccination schedule. The reporter asked if it would be safe for him to receive the second dose (COVID-19 vaccine) on an unspecified date (reported as tomorrow). He has been fever-free for 5 days. Outcome of the event fever was recovered on an unspecified date in Jan2021 and of the other events was unknown. Information on the lot/ batch number has been requested.

Other Meds:

Current Illness:

ID: 1000053
Sex: F
Age:
State: NJ

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

Lab Data:

Allergies:

Symptoms: Woke up 1:30 AM with rigors for 2 hours; woke up in puddle of sweat; felt hungover; malaise; slept most of the day; sore arm; This is a spontaneous report from a contactable consumer. A 25-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK 9231), via an unspecified route of administration on 14Jan2021 at a single dose on Left arm for COVID-19 immunization. Medical history included none. No concomitant medications were received. The patient previously received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, "lot unknown=False"), via an unspecified route of administration on an unspecified date for COVID-19 immunization. The patient woke up 1:30 AM on 14Jan2021 with rigors for 2 hours; after that fell back asleep and woke up in puddle of sweat. In AM felt "hungover"; malaise, slept most of the day and woke up around 5:30 PM; was almost back to normal except sore arm. No treatment received for the event. The outcome of the event sore arm was not recovered while the rest of the events was recovered on 14Jan2021. The events were considered as non-serious. The patient was not pregnant at the time of vaccination. Facility where the most recent COVID-19 vaccine was administered was Hospital. No other vaccines received within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1000054
Sex: F
Age:
State: MI

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

Lab Data:

Allergies:

Symptoms: Swollen lymphnodes in the left collarbone area and my neck; Sore arm; This is a spontaneous report from a contactable consumer. A 23-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3248 and expiration date not provided), via an unspecified route of administration in the left arm on 15Jan2021 14:00 at a single dose for COVID-19 immunization. The patient's medical history was not reported. The patient was not pregnant at the time of vaccination. The patient did not receive any other vaccine within 4 weeks prior to the COVID vaccine. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included ethinylestradiol, norgestimate (SPRINTEC), and sambucus nigra (ELDERBERRY). On 16Jan2021 06:00, the patient experienced sore arm. Then on 17Jan2021 14:00 (reported as 48 hours after vaccination), the patient experienced swollen lymph nodes in the left collarbone area and on her neck on the same side as vaccination. Treatment was not provided in response to the events. The outcome of the events was recovering. The patient has not been tested for COVID-19 since vaccination.

Other Meds: SPRINTEC; ELDERBERRY [SAMBUCUS NIGRA]

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm