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: 0980866
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: left arm sore after first dose injection administered; This is a spontaneous report from a contactable consumer. A 71-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Solution for injection, lot number: EK5730; expiration date not provided), via an unspecified route of administration on 23Dec2020 09:00 at a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient reported that she had first dose of Pfizer COVID-19 Vaccine on 23Dec2020; she reported left arm sore after first dose injection administered. The patient recovered completely from the event after about 4 days on 27Dec2020.

Other Meds:

Current Illness:

ID: 0980867
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Flu like symptoms; feeling achy; Left arm sore after second dose injection administered initially described as at the injection site; This is a spontaneous report from a contactable consumer (patient). A 71-year-old female patient received second single dose of BNT162B2 (Pfizer COVID-19 Vaccine, Solution for injection, lot number: EK9231, exp date: Apr2021), via an unspecified route of administration (Injection to left upper arm ) on 13Jan2021 09:00 for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received first single dose of BNT162B2 (lot number: EK5730) on 23Dec2020 for COVID-19 immunization wherein she reported left arm sore after first dose injection administered which she recovered completely from after about 4 days (from 23Dec2020 to 27Dec2020). The patient called to ask if it was ok to take something like Ibuprofen or paracetamol (TYLENOL) after having been administered Pfizer COVID-19 Vaccine. She reported left arm sore after second dose injection administered on 13Jan2021 and flu like symptoms on an unspecified date. The left arm sore after first dose injection administered was same reaction she had following the second dose: Left arm sore after second dose injection administered initially described as at the injection site; very sore; her arm being much better since she slept all last night with ice pack on her left arm; but then specified that outcome of that event and flu like symptoms have remained persistent with on and off pattern; The flu like symptoms include feeling achy which started on 14Jan2021 (day of reporting). The outcome of events was not recovered.

Other Meds:

Current Illness:

ID: 0980868
Sex: F
Age:
State: TX

Vax Date: 01/05/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 20210113; Test Name: COVID-19; Test Result: Positive

Allergies:

Symptoms: allergies; positive for COVID 19; positive for COVID 19; This is a spontaneous report from a contactable consumer(patient) from Pfizer-sponsored program Pfizer First Connect. The 24-year-old female consumer received first dose of bnt162b2 (BNT162B2, lot number: 1686), unknown on 05Jan2021 at SINGLE DOSE by injection once to left arm for covid-19 immunisation. Medical history and concomitant medications were none. The patient got the first dose of the COVID 19 vaccine and got positive for COVID 19 on 13Jan2021, and is asking if she will have to take the second dose as per her scheduled date. States she thought this was just allergies, since she takes Zyrtec and it clear up everything. No further details provided. The outcome of the event drug allergy was unknown and was not recovered for the rest events. No follow-up attempts possible. No further information expected.

Other Meds:

Current Illness:

ID: 0980869
Sex: F
Age:
State: MI

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

Lab Data:

Allergies:

Symptoms: Flushed; Hot feeling; Numb back of tongue or throat; Numb back of tongue or throat; This is a spontaneous report from a contactable nurse (patient). A 35-year-old female patient (non-pregnant) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EL0142), intramuscular in left arm, on 08Jan2021 at 12:00, at a single dose, for COVID-19 immunization. The patient's medical history included Bell's palsy from 2017. The patient's concomitant medications were not reported. The patient previously took the first dose of BNT162B2 on 18Dec2020 at 12 PM for COVID-19 immunization (intramuscular in right arm) and experienced flushed and hot feeling. The patient had no known allergies. The patient was not diagnosed with COVID-19 prior vaccination. The vaccine was administered in a hospital facility. On 08Jan2021 (12:30 PM), the patient experienced flushed or hot feeling 30 minutes after the second dose, followed by numb back of tongue or throat (best described like swallowing a good amount of throat numbing spray) that lasted about 2 hours. No treatment was administered for the events. The patient had not been tested for COVID-19 post-vaccination. The patient recovered from the events on 08Jan2021 (14:30).

Other Meds:

Current Illness:

ID: 0980870
Sex: U
Age:
State:

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

Lab Data:

Allergies:

Symptoms: fever; headache; chills; body aches, especially in my back; body aches, especially in my back; This is a spontaneous report from a contactable consumer. A patient of unspecified age and gender 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 single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient previously took first dose of bnt162b2 (lot number and expiry date not reported) on an unspecified date at single dose for COVID-19 immunisation and experienced painful, swollen axillary lymph node. It was reported that after the second dose, the patient had a rougher go of it with fever, headache, chills, body aches, especially in back. Clinical outcome of the events was unknown. Information on the lot/ batch number has been requested.

Other Meds:

Current Illness:

ID: 0980871
Sex: F
Age:
State: CA

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Stomach ache; Restless; Couldn't sleep; Headache; So hot she couldn't keep cool; This is a spontaneous report from a contactable consumer (patient). A 98-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: EL8982, expiration date not reported) via an unspecified route of administration at the left arm on 12Jan2021 15:45 at a single dose for COVID-19 immunization. The patient's medical history included arthritis, she is in a wheelchair (can't walk), gallbladder out a year ago (2020) and she her right hip replaced. No family medical history. There were no concomitant medications. The patient usually sleeps well. Clarified she received the first dose of the Pfizer COVID 19 vaccine 12Jan2021 15:45PM in the left arm. She was fine after the injection then 13Jan2021 in the afternoon she had a headache for two hours; that night she was restless and couldn't sleep; she was so hot she couldn't keep cool. Then this morning 14Jan2021 her headache is gone but she has a little stomach ache. Mentioned they haven't brought breakfast by yet and that might help. She was planning to get the next dose of the vaccine 02Feb2021. She has been living in an assisted living facility now for three years; and she can't get outside; and has not seen her family due to the virus. The facility where the vaccine was administered was in an assisted living facility. There were no additional vaccines administered on same date of Pfizer suspect. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The events did not require a visit to physician or ER. No relevant tests done. Outcome of the events headache, feeling hot, restless was recovered on 14Jan2021; stomach ache was recovering and unknown for the other event.

Other Meds:

Current Illness:

ID: 0980872
Sex: M
Age:
State: VA

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

Lab Data:

Allergies:

Symptoms: Very cold; Headache; issues with his lower extremities; he cannot walk; Body does not work anymore; Throwing up; bad feeling; This is a spontaneous report from a contactable consumer (patient). A 75-year-old male patient received the first dose of BNT162B2 (Pfizer-BIONTECH Covid-19 Vaccine; Lot number: LE3301), via an unspecified route of administration in the right arm on 12Jan2021 at 15:30 as a single dose for COVID-19 immunisation. Medical history included belief that he had agent orange and tiredness. The patient did not have additional vaccines administered on the same date as the Pfizer vaccine and did not have vaccinations within four weeks. The patient's concomitant medications were not reported. The patient previously received a flu shot in October (year unspecified). On 12Jan2021, the patient was throwing up. The patient stated that his whole body has gone, it did not work anymore, his legs have gone out, and was having headaches on 13Jan2021. The patient initially stated that the feeling that his body did not work anymore started six hours after he got the vaccine. He later clarified and stated it started on 13Jan2021. He further clarified that what he meant by the body did not work was issues with his lower extremities, he cannot walk and he was having a lot of headaches. The throwing up started on the evening of 12Jan2021. He could not get up to go to the bathroom. He had a couple of episodes of throwing up. He confirmed the throwing up has resolved, but was unable to provide any additional details. He also added that he was feeling very cold on 13Jan2021. The headaches left him concerned. At end of the call, the patient indicated he wanted this bad feeling to go away. The events did not require any visit to the Emergency Room or Physician's office (patient stated he considered it, but he just stayed in bed). Outcome of the event throwing up was recovered, for the events body does not work anymore, very cold, and headache was not recovered, while for the other events was unknown.

Other Meds:

Current Illness: Disability

ID: 0980873
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: headache; This is a spontaneous report from a contactable consumer (reporting for herself). A 43-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. Medical history included headache during menses. The patient's concomitant medications were not reported. The patient experienced headache on an unspecified date. During the time of vaccination, the patient was on her menses. Therapeutic measures were taken as a result of headache and included over the counter (OTC) medication. The clinical outcome of headache was recovered on an unspecified date. The batch/lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 0980874
Sex: F
Age:
State:

Vax Date: 01/14/2021
Onset Date: 01/17/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: tingling in my throat; tingling on the tongue and bottom lip; Burning sensation in my throat, on the tongue and bottom lip and on the left side of the face as well; tingling sensation developed on the left side of the face; This is a spontaneous report from a non-contactable pharmacist reporting for herself. A 33-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: El1283), via an unspecified route of administration on 14Jan2021 at single dose in left arm for COVID-19 immunisation. Patient age at time of vaccination was 33 years. The vaccine was administered in the Clinic. No other vaccine was given within 4 weeks prior to the COVID vaccine. Medical history included migraine very infrequent. Concomitant medications included norethisterone (NORETHINDRONE). The patient had no known allergies. She reported that slightly over 48 hours post injection on 17Jan2021 she developed a tingling and burning sensation in throat, on the tongue and bottom lip. A burning or tingling sensation developed on the left side of the face as well. Treatment for the events included Benadryl. The patient had not recovered from the events at the time of the report. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, she has not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Other Meds: NORETHINDRONE [NORETHISTERONE]

Current Illness:

ID: 0980875
Sex: M
Age:
State: MI

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

Lab Data:

Allergies:

Symptoms: Flu like symptoms including body aches; Flu like symptoms including body aches; alternating fever and chills on the second dose; alternating fever and chills on the second dose; This is a spontaneous report received from a contactable consumer. A 35-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL0142, expiry date: unknown), via an unspecified route of administration, on 13Jan2021, at single dose, for COVID-19 immunization. The patient medical history and concomitant medications were not reported. It was unknown if the patient had COVID-19 prior to vaccination. Historical vaccine included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1685, expiry date: unknown), via an unspecified route of administration, on 23Dec2020, for COVID-19 immunization and had a sore shoulder (at point of injection) and foggy head for the few hours. On 14Jan2021 at 06:30, the patient experienced flu like symptoms including body aches, alternating fever and chills on the second dose. Treatment was not given for the events. It was unknown if the patient was tested for COVID-19 post vaccination. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 0980876
Sex: M
Age:
State: AR

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 20210113; Test Name: Fever; Result Unstructured Data: Test Result:102.3 Fahrenheit

Allergies:

Symptoms: Flu like symptoms; Fever of 102.3; This is a spontaneous report from a contactable consumer(patient). A 36-year-old male received second dose BNT162B2 (Pfizer BioNTech Covid 19 vaccine, lot number EL3246), via an unspecified route of administration at Arm Right on 12Jan2021 17:00 at the 36 years old at single dose for COVID-19 immunization. The medical history included High cholesterol. The concomitant medications were Hydroxychloroquine and azithromycin( ZITHROMAX Z-PACK). The Historical Vaccine was first dose BNT162B2 (Lot number=EL1284)on 22Dec2020 17:00 at 36 years old at Left arm for COVID-19 immunization and experienced Covid test result Positive on 30-DEC-2020. The patient previously took Codeine and experienced Allergy. On 13Jan2021 16:00 the patient experienced Flu like symptoms and fever of 102.3 Fahrenheit at 23 hours after the second dose. There was no treatment received for the adverse events. 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 outcome of the events was recovering.

Other Meds: HYDROXYCHLOROQUINE; ZITHROMAX Z-PACK

Current Illness:

ID: 0980877
Sex: F
Age:
State: KS

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

Lab Data: Test Name: temperature; Result Unstructured Data: Test Result:97.3

Allergies:

Symptoms: generally weak; Pale; Headache; migraines; feels foggy; Hard time concentrating; pain in her shoulder, she thought it was cause of the injection site/muscle pain from the injection; pain in shoulder immediately after getting the injection and it was really swollen; body is in pain/lot of pain all of her body; achy like she is having flu like symptoms; injection was administered higher in her left shoulder; This is a spontaneous report from a contactable consumer (patient). A 57-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: unknown), via an unspecified route of administration on 12Jan2021 (16:00) at single dose for Covid-19 immunization. The patient received the first dose of BNT162B2 (lot number: EK9231) injection in left deltoid/shoulder on 22Dec2020 at single dose for Covid-19 immunization. The patient's medical history was reported as "none". There were no concomitant medications. It was reported that the patient received the first dose on 22Dec2020 and the second dose on 12Jan2021. After she received the second dose of the vaccine, she immediately had pain in her shoulder, she thought it was cause of the injection site (12Jan2021 16:00). She had the pain in shoulder immediately after getting the injection and she got it at 4pm, and it was really swollen now. She mentioned this injection was administered higher in her left shoulder (pending clarification) and it feels like they may have gotten the injection in more of the arm muscle and she was thinking that is why she had muscle pain from the injection. She added that it was like her body is in pain, achy like she is having flu like symptoms that started the evening she got the vaccine, like 6PM or 7PM. The next day, yesterday (13Jan2021), she had a lot of pain all of her body. She also started to have a headache yesterday at noon (13Jan2021 12:00PM). The headache started at noon on 13Jan2021 and it continued for at least 8 hours and it was constant. It started to subside over the next 12 hours. She mentioned she also suffers from migraines (pending clarification). It feels like she is having residual migraine, like she is coming off of having a migraine. It is presenting, but she is not in severe pain. It is a feeling like she is coming off her migraine medication even though she did not take her migraine medication. She went to work yesterday (13Jan2021) even though she did not feel like it. She went home a few minutes early. She let her supervisor know she was in severe pain and had a headache. She was advised to stay home today and has not gotten better. However, the headache subsided. She feels foggy, like she could not just quite wake up. It is like she is in a daze or haze. She is having a hard time functioning. She continued to reiterate she was having a hard time concentrating. Now (14Jan2021) she is generally weak and is pale. In addition, the pain has not gone away. She stated she is weak, very weak. She felt it most of the day and it is worse today. She feels like she can hardly stand. She is trying to get fluids in her and trying to make coffee, however, it is a struggle. She stated, she has not gone yet, but she will call her doctor's office next and the health nurse as well to advise them she has been having symptoms. She stated she did not have a fever last night. Her temperature during the call was normal for her, 97.3. The outcome of events vaccinations site pain, vaccination site swelling, general body pain, flu like symptoms, weak, and pale was not recovered; while the outcome of other events was unknown. Information on lot/batch has been requested.

Other Meds:

Current Illness:

ID: 0980878
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: Joint pain; Has a little bit of pain in her finger on the left hand; This is a spontaneous report received from a contactable consumer (patient). A 66-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration in the right arm, on 04Jan2021 15:45, at single dose, for COVID-19 immunization, in her workplace. Medical history included ongoing arthritis (has been cold there) and Crohn's disease so the patient has a tendency to have inflammation. Concomitant medication included vedolizumab (ENTYVIO). The patient experienced joint pain and had a little bit of pain in her finger on the left hand on an unspecified date in Jan2021. Treatment included Salonpas and Tylenol. The outcome of joint pain was recovering (reported as ongoing but a little better); and "has a little bit of pain in her finger on the left hand" was unknown. Information on the batch/lot number has been requested.

Other Meds: ENTYVIO

Current Illness: Arthritis (has been cold there)

ID: 0980879
Sex: F
Age:
State: SC

Vax Date: 12/21/2020
Onset Date: 01/07/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 20201229; Test Name: COVID-19 virus test; Test Result: Positive

Allergies:

Symptoms: COVID-19 pneumonia; COVID-19 pneumonia; This is a spontaneous report from a contactable nurse (patient) from a Pfizer-sponsored program IBCC (Inbound Call Center for HCPs). A 45-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot number: EK570), via an unspecified route of administration in the left upper arm on 21Dec2020 at a single dose for COVID-19 immunization. Medical history was none and there were no concomitant medications. The patient stated that she felt yucky afterwards on 23Dec2020, experienced shortness of breath on exertion and coughing on 26Dec2020; chills, dizziness, headache, muscle pain, body aches, fever on 28Dec2020; loss of taste, loss of smell and COVID-19 pneumonia on 07Jan2021. All the events were reported as being medically significant. The patient underwent lab tests and procedures which included COVID-19 virus test: positive on 29Dec2020. Therapeutic measures were taken as a result of COVID-19 pneumonia and included: started on bronchodilator, cough elixir, steroids and azithromycin (ZITHROMAX). The outcome of muscle pain, body aches and COVID-19 pneumonia was recovering and of loss of taste and loss of smell was not recovered. The causality of the suspect vaccine to the events was reported as related.; Sender's Comments: A causal association between BNT162B2 and the reported events cannot be excluded based on a compatible temporal relation. However, full immunity is only expected 2 weeks after the second dose.

Other Meds:

Current Illness:

ID: 0980880
Sex: F
Age:
State: CA

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

Lab Data:

Allergies:

Symptoms: left upper arm swelling; neck pain, mainly on left side; Headache; left sided facial swelling; This is a spontaneous report from a contactable nurse (patient herself). A 49-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number EL1284, expiry date Apr2021), via an unspecified route of administration on 13Jan2021 at a single dose in the left arm for immunity (COVID-19 immunisation). There were no medical history and concomitant medications. The patient received the COVID vaccine and developed some symptoms on 13Jan2021. The symptoms were: left upper arm swelling, neck pain, mainly on left side, a headache, and left sided facial swelling. The patient had not recovered from the event headache. The outcome of the events left upper arm swelling, neck pain and left sided facial swelling was recovering. The events left upper arm swelling, neck pain, mainly on left side and relatedness left sided facial swelling with COVID vaccine was related.

Other Meds:

Current Illness:

ID: 0980881
Sex: F
Age:
State: FL

Vax Date: 12/21/2020
Onset Date: 12/21/2020
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: a little sore on site on the first day; This is a spontaneous report from a contactable nurse (patient). An 81-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: EH9899, expiry date: 31Mar2021), via an unspecified route of administration on 21Dec2020 at a single dose for covid-19 immunization. Medical history included colitis, diverticulitis and allergies. Concomitant medications included chlordiazepoxide hydrochloride, clidinium bromide (LIBRAX [CHLORDIAZEPOXIDE HYDROCHLORIDE;CLIDINIUM BROMIDE]) for colitis, omeprazole (PROTONIX [OMEPRAZOLE]), cetirizine hydrochloride (ZYRTEC [CETIRIZINE HYDROCHLORIDE]) for allergies, and cyanocobalamin, folic acid (VITAMIN B12 & FOLIC ACID) for colitis. The patient experienced a little sore on site on the first day on 21Dec2020. Outcome of the event was recovered on 22Dec2020.

Other Meds: LIBRAX [CHLORDIAZEPOXIDE HYDROCHLORIDE;CLIDINIUM BROMIDE]; PROTONIX [OMEPRAZOLE]; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; VITAMIN B12 & FOLIC ACID

Current Illness:

ID: 0980882
Sex: M
Age:
State: IL

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

Lab Data:

Allergies:

Symptoms: fever; chills; severe body aches; This is a spontaneous report from a contactable physician (patient). A 45-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date unknown) intramuscular at the right arm on 13Jan2021 14:30 at single dose for Covid-19 immunization in a hospital. Medical history and concomitant medications were none. Historical vaccines included first dose of BNT162B2 on 23Dec2020 for Covid-19 immunization and with a week (30Dec2020 16:15) he developed COVID positive test, had a mild to moderate illness. The patient received second dose and developed fever, chills and severe body aches on unspecified date in Jan2021. The outcome of the events fever, chills and severe body aches was unknown. Follow-up activities are possible, information on the batch number has been requested.

Other Meds:

Current Illness:

ID: 0980883
Sex: F
Age:
State: OK

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

Lab Data:

Allergies:

Symptoms: felt really tired; eyes has a burning feeling behind them; joint pain; This is a spontaneous report from a contactable consumer (patient). A female patient of unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date unknown) via unspecified route of administration on 13Jan2021 at single dose for Covid-19 immunization. Medical history and concomitant medications were not reported. The patient received her first dose of the COVID-19 vaccine yesterday, 13Jan2021. The patient informed that she felt really tired now, and her eyes has a burning feeling behind them, and she has joint pain (Jan2021). The patient wanted to know how long do the side effects last. The outcome of the events felt really tired, eyes has a burning feeling behind them, joint pain was unknown. Follow-up activities are possible, information on the batch number has been requested.

Other Meds:

Current Illness:

ID: 0980884
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Extreme fatigue; Malaise; chills; Injection site pain and tenderness; muscular pain; This is a spontaneous report from a non-contactable physician (reporting for herself). A non-pregnant 34-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration in the left arm on 13Jan2021 6:00 PM at a single dose for COVID-19 immunization. Medical history included: COVID-19 (prior to the vaccine). The patient's concomitant medications were not reported. The patient had no known allergies. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), on 24Dec2020 3:00 PM in the left arm, at 34 years old for COVID-19 immunization. The patient experienced extreme fatigue, malaise, chills, injection site pain and tenderness and muscular pain on 14Jan2021. Therapeutic measures were taken as a result of the events which included ibprophen (ADVIL). The outcome o the events was recovered in Jan2021. No follow-up attempts are possible; information about batch/lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 0980885
Sex: M
Age:
State: TX

Vax Date: 12/28/2020
Onset Date: 01/11/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: Covid-19; Test Result: Positive

Allergies:

Symptoms: Tested positive for COVID; Tested positive for COVID; This is a spontaneous report from a contactable consumer (patient's daughter) via the Pfizer sponsored program Pfizer First Connect. An 88-year-old male patient started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration from 28Dec2020 to 28Dec2020 at SINGLE DOSE for covid-19 immunisation. Medical history included was reported as none. There were no concomitant medications. The reporter stated that the patient had tested positive for covid on 11Jan2021. Outcome of the event was unknown. Information on the Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980886
Sex: F
Age:
State: NC

Vax Date: 01/10/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: hasn't slept all night; Itching; This is a spontaneous report from a contactable consumer (patient). An 84-year-old female patient received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, lot number unknown and has been requested), via an unspecified route of administration on 10Jan2021 at single dose because COVID is getting worse and she is in a home. Medical history included 17 back surgeries, has lost a good bit of weight, ongoing pain, ongoing arthritis and ongoing sleep disorder. Concomitant medication included hydrocodone bitartrate, paracetamol (manufacturer unknown) from an unknown date and unknown if ongoing and morphine pump (manufacturer unknown) for pain which she has had for eight years that is right under the skin. The patient was also taking something (unspecified) for arthritis and they give her something (unspecified) to help her sleep. The patient got her first shot on Sunday, 10Jan2021. She has not had effects or anything. However on 13Jan2021, she started itching. She stated that honest to God she hasn't slept all night on an unspecified date. She is itching all over. She wanted to know if this was something that comes with the vaccine. She thought if she would have something it would have happened on Monday or Tuesday and at the time of the report it was Thursday. She stated that she was not that concerned. She was just calling to pass this along. She added that she is in good shape structurally. She was not worried as someone might have the same effect. This could just be side effects. The outcome of the event itching was recovering while the outcome of the event hasn't slept all night was unknown. Information on the Batch/Lot number has been requested.

Other Meds: HYDROCODONE/ACETAMINOPHEN; MORPHINE

Current Illness: Arthritis; Pain; Sleep disorder

ID: 0980887
Sex: F
Age:
State: NM

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

Lab Data:

Allergies:

Symptoms: tired; slept most of the day; Headache; Chills; Joint pain; Sore throat; muscle pain/muscle ache; arm was hurting more than sore/arm pain at injection site; Nausea; Loose stools; Left eye twitching; feeling pretty ill/ under the weather; a little short of breath/shortness of breath; Metal taste in her mouth; Itchy everywhere; asthma has flared up a little bit; This is a spontaneous report from a contactable consumer (patient). A 37-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number EH3246, expiry date unknown), intramuscular (right arm), on 08Jan2021, at single dose, for covid-19 immunization. Medical history included asthma since 2004 (diagnosed about 17 years ago). Concomitant medication included formoterol fumarate, mometasone furoate (DULERA) (has been on this for about 2 months) for asthma. The patient previously took formoterol and budesonide (SYMBICORT) for asthma. The patient stated she was a technician and she has a couple of questions about the Covid vaccine. She got the vaccine on 08Jan2021. Since she got the vaccine, papers said she would feel under the weather for a few days but she was still feeling pretty ill; she wanted to know if this was normal and when should she be concerned, wondering if she should call her doctor. She was encouraged to reach out to her HCP for any medical advice. She also stated that 5-10 min after the vaccine on 08Jan2021, she started to feel a little short of breath/shortness of breath but that resolved. Also, afterwards on 08Jan2021 she had a metal taste in her mouth and was itchy everywhere on that day. She went home and around 9PM on the day of the vaccination, she started to feel under the weather on 08Jan2021. Then she woke up on Saturday 09Jan2021 with headaches, chills, joint pain, sore throat, muscle pain/muscle ache, arm was hurting more than sore/arm pain at injection site, nausea, loose stools, and left eye twitching. On Sunday 10Jan2021, she was very tired and slept most of the day. She added that she has been reporting this to the link that was provided to her. She has been taking Tylenol and ibuprofen to treat these symptoms and; was also using her inhaler because it seemed like asthma has flared up a little bit on Jan2021. No other vaccines administered on the same date with the Pfizer vaccine. The adverse events did not require a visit to the emergency room or physician office. No prior vaccinations within four weeks. The outcome of the events feeling pretty ill/ under the weather, slept most of the day and, asthma has flared up a little bit was unknown. The outcome of events a little short of breath/shortness of breath, metal taste in her mouth, and itchy everywhere was recovered on 08Jan2021. The outcome of joint pain was recovering. The outcome of arm was hurting more than sore/arm pain at injection site was recovered on 13Jan2021. The outcome of the other remaining events was not recovered.

Other Meds: DULERA

Current Illness:

ID: 0980888
Sex: F
Age:
State: CA

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

Lab Data: Test Name: blood cells; Result Unstructured Data: Test Result:6.4; Test Date: 202007; Test Name: blood tests; Result Unstructured Data: Test Result: all her blood work was fine; Test Date: 202010; Test Name: blood tests; Result Unstructured Data: Test Result: all her blood work was fine; Comments: daily blood tests performed; Test Date: 202011; Test Name: COVID-19 test; Result Unstructured Data: Test Result: Unknown results

Allergies:

Symptoms: She said maybe she is experiencing a drug interaction between the antibiotic and the COVID-19 Vaccine; woke up early this morning with a rash from head to toe, saying the rash is really itchy; she had big, red welts when she first woke up this morning; This is a spontaneous report from a contactable consumer reporting for herself. A 62-year-old female patient received first dose of bnt162b2 (BNT162B2, lot number: EL1283, expiry date: not reported), via an unspecified route of administration, on 11Jan2021 12:00PM at a single dose on deltoid, right for COVID-19 immunization. Vaccination Facility Type was clinic facility. The patient also took sulfamethoxazole, trimethoprim (BACTRIM, tablet, lot number and expiry date were not reported), oral, from an unspecified date and ongoing, at 1 DF, 2x/day for urinary tract infection (UTI). She was prescribed 10 sulfamethoxazole, trimethoprim tablets, and has been taking 1 tablet by mouth, twice a day. She said she was prescribed a 5-day treatment course, and she has 1 dose left at the time of report, 14Jan2021. Medical history included colon cancer from 2018, sigmoid colon and part of her descending colon were removed, septic shock, ureter was severed, colostomy, nephrostomy, ileostomy, frequent UTIs, bowel obstruction, several stents placed in her colon due to the strictures, coded in the ICU, was on a ventilator, sigmoidoscopy, anemic from an unspecified date to an unspecified date (does not have a problem with anemia anymore), blood transfusions, was in the hospital for a week at the end of Jul2020 to an unspecified date. She reported she had colon cancer 2 years ago that was 1 encapsulated tumor, so she didn't need chemo or radiation. She said her sigmoid colon and part of her descending colon were removed. She had severe complications after the surgery: her resection ruptured, she had septic shock and her ureter was severed. She had a colostomy and nephrostomy at the same time and then an ileostomy after the colostomy was taken down. She has frequent UTIs due to no backflow valve from her ureter to her kidney. She said she has had so much work on her colon, she has constant strictures resulting in bowel obstructions. She said she has had several stents placed in her colon due to the strictures. She said she didn't know if her previous medical history has anything to do with the rash she is experiencing now. She said when she had septic shock, she coded in the ICU and was on a ventilator. No further details provided. Reported she had a COVID-19 test done in Nov2020 prior to having a follow-up sigmoidoscopy at the hospital. She said her primary care doctor set her up to have a thyroid panel, CBC, and lipid panel done, and she will going to have those tests shortly. She said she had daily blood tests performed when she was in the hospital for a week in Oct2020, and when she was in the hospital for a week at the end of Jul2020. She said all her blood work was fine during those hospital stays. No further details provided. She was anemic in the past due to her colon cancer, but she does not have a problem with anemia anymore. She said at one point her red blood cells were down to 6.4 and she needed to get blood transfusions. Concomitant medications were none. The patient previously received a flu vaccine in Oct2020. The patient did not have other vaccinations within 4 weeks prior to receiving bnt162b2. The patient reported she had the COVID-19 Vaccine on Monday, 11Jan2021, in the afternoon, clarified as 12:00PM. She had to wait 20-30 minutes after receiving her first COVID-19 Vaccine dose to make sure she had no reaction. She woke up early this morning (14Jan2021) with a rash from head to toe, saying the rash is really itchy. She had big, red welts when she first woke up this morning. She said she is not experiencing any pain, fever, or anything else. She said she has had no reactions to vaccines before. She is wondering if it makes any difference, but she had a UTI prior to taking the COVID-19 Vaccine. She said she has been taking antibiotics for the UTI. She said maybe she is experiencing a drug interaction between the antibiotic and the COVID-19 Vaccine, and that could have contributed to her rash. She first noticed the head to toe rash this morning. She said she initially woke up at 4:30AM and had a bowl of cereal. She said at that time she didn't notice anything different and went back to bed. When she woke up later on, and looked in the mirror, she saw she was covered in a rash. She had a scheduled video conference with her doctor yesterday, 13Jan2021, and her doctor is unaware that she developed a rash since then. Her rash doesn't look as red as when she first woke up this morning. She said she dare says that the rash possibly improved a little. She said there are no big, red welts like when she first woke up this morning. She said she can live with the rash but wants to know if she still can get her second COVID-19 Vaccine dose. Her second COVID-19 Vaccine dose is scheduled on 01Feb2021. She said she wants to know if the rash is going to prevent her from getting the second COVID-19 Vaccine dose. She said she is terrified of getting the COVID-19 Virus. She said her husband wouldn't survive if he got the COVID-19 Virus. She asked if a rash is common after receiving the COVID-19 Vaccine, and if the rash will go away on its own. The action taken in response to the events for sulfamethoxazole, trimethoprim was unknown. The patient did not receive any corrective treatment for the reported adverse events. She has considered taking an antihistamine but was going to wait until she finishes her coffee to see how she feels. She clarified at the end of the call that her rash was not as bad as when she first noticed it, saying the rash is getting a little better. The adverse events did not require emergency room or physician office visit. Outcome of the events was recovering.

Other Meds: BACTRIM

Current Illness:

ID: 0980889
Sex: F
Age:
State:

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data: Test Date: 20210112; Test Name: Rapid COVID-19 nasal swab test; Test Result: Negative

Allergies:

Symptoms: Muscle pain; Chills; Nausea; This is a spontaneous report from a contactable consumer. A 60-year-old female 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 in left upper arm on 11Jan2021 around 3:45-4:00pm at a single dose for COVID-19 vaccination. Medical history included hypothyroidism. Concomitant medication included levothyroxine from 2006 for hypothyroidism. The patient was administered the first dose of Pfizer-BioNTech COVID Vaccine on 11Jan2021 at work. On 12Jan2021, the patient experienced muscle pain, chills, nausea. The outcome of the events was not recovered. The patient underwent rapid COVID-19 nasal swab test and the result was negative on 12Jan2021. Second dose scheduled to be administered on 01Feb2021 with no dose change made. Information on the Lot/batch number has been requested.

Other Meds: LEVOTHYROXINE

Current Illness:

ID: 0980890
Sex: F
Age:
State: NY

Vax Date: 01/12/2021
Onset Date: 01/14/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: right side of her face swollen; extreme fatigue; This is a spontaneous report from a contactable consumer (patient). An 86-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number EL3246, expiration date not reported), intramuscular on the upper left arm, on 12Jan2021 at a single dose to develop immunity for Covid 19 virus. The patient has no medical history. Concomitant medication included ongoing levothyroxine sodium (SYNTHROID). The patient stated she got Pfizer Covid 19 vaccine two days ago at a hospital in the city and right side of her face was swollen and had extreme fatigue on 14Jan2021. Stated she is resting now and is feeling fine. She stated that it happened this morning. Stated that she waited for 15 minutes after the vaccine and had no side effects. She stated that her next dosage is 02Feb2021. There was no treatment received for right side of face swelling. Outcome of the events was recovering.

Other Meds: SYNTHROID

Current Illness:

ID: 0980891
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: Right arm killing her through the night; Little Achy; Headache; This is a spontaneous report from a contactable consumer (patient herself). A 71-year-old female patient received bnt162b2 (BNT162B2 also reported as Pfizer COVID Vaccine, lot EL3247), intramuscular in the right arm on 13Jan2021 18:00 at SINGLE DOSE for Covid-19 immunisation (reported as prevention for age group). She received the vaccine in a hospital. Medical history included a Covid-19 patient on Mar2020, hypothyroidism and normally had headaches. No other vaccines taken prior to vaccination. There were no concomitant medications. On 13Jan2021 03:00, she had arm pain that was killing her through the night. She was a little achy, had a headache, but no fever. The outcome of events was recovering.

Other Meds:

Current Illness:

ID: 0980892
Sex: M
Age:
State: TN

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

Lab Data:

Allergies:

Symptoms: really tired; This is a spontaneous report from a contactable consumer (patient's sister). A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number unknown), via an unspecified route of administration on 08Jan2021 at a single dose for COVID-19 immunization. The patient's medical history included parkinsons. Concomitant medications were not reported. The patient was having a hard time right now. He was really tired on Jan2021 and does not know if he has any other symptoms. Outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 0980893
Sex: M
Age:
State: OK

Vax Date: 01/07/2021
Onset Date: 01/07/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Bruise where he got the shot; Arm soreness; This is a spontaneous report from a contactable consumer (patient). A 70-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; Batch/lot number: EK9231, expiry date: unknown), via an unspecified route of administration on 07Jan2021 at single dose (left arm) for COVID-19 immunization (Over 65 years old; 2nd group to receive in state). The patient medical history was not reported. There were no concomitant medications. Patient got the COVID Vaccine last Thursday (07Jan2021). He had soreness in his arm, which is fine, but when he took the Band-Aid off he had a bruise where he got the shot (13Jan2021). His wife told him he should call and report this. About the arm soreness, it was really sore the first couple of days. The nurse said if he moves his arm and works it, it would help. It was sore for about 2-3 days. Sore to the touch, but not painful. There were no treatment given. They were asking if they should contact his physician, if this is normal. He has had vaccines before, but never had a bruise. The outcome of the event Bruise where he got the shot was not recovered, while for other event was unknown.

Other Meds:

Current Illness:

ID: 0980894
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: headache; This is a spontaneous report from a Pfizer sponsored program Pfizer First Connect from a contactable consumer reporting on herself. A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number /expiration date: not provided), via an unspecified route of administration, on an unknown date as a single dose for COVID-19 vaccination. Relevant medical history and concomitant medication were not provided. On the same date that evening, the patient experienced headache. The patient received treatment for the event which included 2 aceteminophen (TYLENOL). The outcome of the event headache was unknown. Information on the Lot/Batch number has been requested

Other Meds:

Current Illness:

ID: 0980895
Sex: F
Age:
State: AZ

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

Lab Data:

Allergies:

Symptoms: migraine from sinuses; migraine from sinuses; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (patient) reported that a 39-year-old female patient received BNT162B2, via an unspecified route of administration on 16Jan2021 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 vaccine on 16Jan2021, and she experienced migraine from sinuses. She asked if it is okay to take Migraine medicine while she had her vaccine. The outcome of the events was unknown. Information about Lot/Batch number is requested.

Other Meds:

Current Illness:

ID: 0980896
Sex: M
Age:
State: NC

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

Lab Data:

Allergies:

Symptoms: runny nose; sneezing; don't feel right; This is a spontaneous report from a contactable consumer (patient) via a Pfizer-sponsored program. An 82-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection, unknown lot number and expiration), via an unspecified route of administration on 14Jan2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced side effects after receiving the COVID-19 vaccine on 14Jan2021. The patient experienced runny nose, sneezing and he don't feel right in Jan2021. He is also concerned about his wife if there is a possibility of infecting her since she doesn't have received the COVID-19 vaccine yet. Outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980897
Sex: F
Age:
State: NC

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

Lab Data:

Allergies:

Symptoms: Chills; Extreme fatigue; This is a spontaneous report from a contactable physician (sister in law). A 32-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 11Jan2021 at single dose for COVID-19 immunization. The patient medical history and 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 and did not experienced adverse side effects. On 11Jan2021, the patient experienced chills and extreme fatigue (developed 12 hours after injection). The patient outcome of the events was recovered on 12Jan2021 (after a night of rest). The information on the batch number has been requested.

Other Meds:

Current Illness:

ID: 0980898
Sex: F
Age:
State:

Vax Date: 01/07/2021
Onset Date: 01/16/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: fever; injection site reaction; flulike symptoms; This is a spontaneous report from a contactable Other HCP via Pfizer Sales Representative. A 32-years-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 medical history was not reported. The patient's concomitant medications were not reported. On 16Jan2021, the patient developed injection site reaction, fever, and flulike symptoms after being administered the second dose of the Pfizer/BioNTec COVID-19 vaccine. The patient's symptoms have since resolved on Jan2021. No follow-up attempts are Possible; Information about batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0980899
Sex: U
Age:
State: MI

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

Lab Data:

Allergies:

Symptoms: lips, mouth and tongue were numb; This is a spontaneous report from a contactable nurse (patient) via a Pfizer sponsored program. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 06Jan2021 at single dose for COVID-19 immunization. Medical history included diagnosed with COVID on 03Nov2020. Ever since the patient had had COVID. The patient had a terrible burning sensation in mouth and tongue. The patient's concomitant medications were not reported. Immediately after the vaccine, the pateint's lips, mouth and tongue were numb and felt full, lasted for approx 2 hours. Later that evening the burning the patient had since recovering from covid had stopped. The outcome of the event was unknown. Information on the lot/batch number had been requested.

Other Meds:

Current Illness:

ID: 0980900
Sex: M
Age:
State:

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

Lab Data:

Allergies:

Symptoms: fever; chills; This is a spontaneous report from a contactable consumer. A 60-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on an unspecified date as the second single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced fever and chills on an unspecified date. The outcome of fever and chills was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0980901
Sex: M
Age:
State: AR

Vax Date: 12/31/2020
Onset Date:
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: It's really itchy on my back; This is a spontaneous report from a Pfizer-sponsored program from a contactable consumer (Patient) A 77-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) on 31Dec2020 at single dose via an unspecified route of administration for COVID-19 immunization. Relevant medical history and concomitant medications were not reported. Patient informed that since an unspecified date it was really itchy on my back, it was no terrible hype but really for the last 3 days (as reported). Patient also mentioned that she should get her booster this coming week (as such). At the time of the reporting event outcome was unknown. The information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0980902
Sex: F
Age:
State: PA

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

Lab Data:

Allergies:

Symptoms: Enlarged lymph nodes surrounding the area where it was injected, one of the lymph nodes is right on my clavicle bone in close proximity; I am also feeling swelling under my armpit and up my neck; This is a spontaneous report from a contactable consumer reported for self. This 38-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose for covid-19 immunisation. Medical history included asthma. Concomitant product included vortioxetine hydrobromide (TRINTELLIX). The patient previously the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) for covid-19 immunisation. The patient got the COVID Vaccine second booster on Sunday and was having enlarged lymph nodes surrounding the area where it was injected. The patient stated, "No, it's not at the site of injection, I have one so it's on, I got the shot in my left shoulder and one of the lymph nodes is right on my clavicle bone in close proximity and I am also feeling swelling under my armpit and up my neck." Treatments included Tylenol and Advil. Outcome of the events were unknown. Information about lot/batch number has been requested.

Other Meds: TRINTELLIX

Current Illness:

ID: 0980903
Sex: F
Age:
State: WA

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

Lab Data:

Allergies:

Symptoms: Arm soreness; This is a spontaneous report from a contactable pharmacist (patient). A 43-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899), via an unspecified route of administration on 23Dec2020 12:30 at a single dose for COVID prevention. Medical history included diabetic (On insulin only. Diabetic for six to seven years and have had no hypoglycemic events). There were no concomitant medications. It was reported that the patient experienced arm soreness on an unspecified date. The outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 0980904
Sex: F
Age:
State: MD

Vax Date: 01/12/2021
Onset Date: 01/13/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Lymphadenopathy; mild fatigue; Myalgia; This is a spontaneous report from a contactable physician (patient). A 52-year-old female patient received the second dose of BNT162B2 (Pfizer-BIONTECH Covid-19 Vaccine), intramuscular in the left arm on 12Jan2021 at 16:30 as a single dose to prevent COVID. The patient's concomitant medications were not reported and it was reported that she had no relevant medical history. The patient previously received the first dose of BNT162B2 on 22Dec2020 at 14:00. The patient did not receive any other vaccine/s on the same date as BNT162B2, did not have prior vaccination within four weeks of receiving BNT162B2, and did not experience any adverse event following prior vaccinations. The patient experienced mild fatigue and myalgia on 13Jan2021, and lymphadenopathy on 14Jan2021. Seriousness for the events was reported as serious (medically significant). The patient received her second dose of the Pfizer Covid Vaccine on 12Jan2021 at 16:30. She experienced mild fatigue and myalgia after 24 hours which has improved. She clarified that the mild fatigue and myalgia resolved by this morning. She felt lymphadenopathy in her lower neck and supraclavicular area. Stated it was almost fullness she can feel, there was no redness and it was not tender. She was hoping this was related to the vaccine that she got in her left upper arm. She went to the CDC and Pfizer website and saw that lymphadenopathy was mentioned but it was a small percentage. The patient declined any treatment. The events did not require a visit to the Emergency Room of Physician's office. Outcome of the events fatigue and myalgia was recovered on 15Jan2021, while for the event lymphadenopathy was not recovered. The reporter's causality assessment between the events and BNT162B2 for the events fatigue and myalgia was related, while for the event lymphadenopathy was unknown. Information about the lot/batch number has been requested.; Sender's Comments: Based on the compatible time association and drug's safety profile, the events fatigue, myalgia and lymphadenopathy are possibly related to suspect BNT162B2 administration. 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:

Current Illness:

ID: 0980905
Sex: F
Age:
State: TX

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

Lab Data:

Allergies:

Symptoms: three nights of very vivid nightmares; waking up with Panics with worm head; This is a spontaneous report from a contactable pharmacist (patient). A 54-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on the left arm on 11Jan2021 at 13:15 at a single dose in the hospital for COVID-19 immunization. The first dose was received on 19Dec2020 at 13:15 on the left arm for COVID-19 immunization. The reaction with the first dose was losing taste and smell for two days. Medical history included sulfa allergies. Patient is not pregnant at the time of vaccination. The patient's concomitant medications were not reported. The reaction with the 2nd dose was three nights of very vivid nightmares to the point of waking up with panics with worm head. This is not usual and happened the night of the vaccination (11Jan2021) and subsequent two nights. The patient did not receive treatment for the events. Outcome of the events was unknown. No follow-up attempts are possible, information about batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 0980906
Sex: F
Age:
State: IL

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

Lab Data: Test Date: 20210114; Test Name: Body temperature; Result Unstructured Data: Test Result:99.5; Comments: Fever

Allergies:

Symptoms: chills; dizzy; body aches; fever 99.5; fatigue; joint aches; jaw hurts more on Rt side (lower behind12 yr molars); Slept a lot so far; injection arm very sore; This is a spontaneous report from a contactable other healthcare professional (patient). A 52-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number: EL1283), intramuscular on 13Jan2021 09:30 AM at single dose on the right arm for COVID-19 immunization. Patient is not pregnant. The patient medical history was not reported. Concomitant medications included tocopherol (VITAMIN E [TOCOPHEROL]), colecalciferol (D3), estradiol (ESTROGEN), progesterone, "bioidenticle" and multivitamin, reported as "Other medications in two weeks: Multi vitamin, vitamin E, D3, bioidenticle estrogen/progesterone"). The patient previously took iodine, metronidazole (FLAGYL), doxycycline and telithromycin (KETEK) and experienced allergies to all. No other vaccine in four weeks. Facility type vaccine was hospital. The patient received the first dose on 23Dec2020 04:45 PM (lot number: EL0140), intramuscular on the right arm and patient felt slightly light headed. Within 5 minutes right (Rt) hand got red & hot, numb, heat in Rt arm and Rt side of jaw felt numb as if blew up balloons. Blood pressure went up to something over 90. Patient took benadryl. Next few days was reported as "v fatigued & on p.m. of 24th it hurt to open my mouth (gland by Rt ear felt swollen). I got a line of inflammation in my Rt inside cheek & a tissue mound that has not gone away". On 14Jan2021 (reported as today), the patient experienced chills, dizzy, body aches, fever 99.5, fatigue, joint aches, injection arm very sore (started yesterday on 13Jan2021), jaw hurts more on right (Rt) side (lower behind12 yr molars). Patient took Tylenol and slept a lot so far. No treatment was received (If treatment AE: No) - pending clarification. Outcome of the events was recovering. Patient has no COVID prior vaccination. Patient was not tested for COVID post vaccination.

Other Meds: VITAMIN E [TOCOPHEROL]; D3; ESTROGEN; PROGESTERONE

Current Illness:

ID: 0980907
Sex: F
Age:
State: OK

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

Lab Data:

Allergies:

Symptoms: Vertigo/dizzy/room spins starting; dizzy/room spins starting; Fatigue; Sore body; HA (headache); Nausea; Racing thoughts; trouble sleeping; This is a spontaneous report from a contactable nurse (patient). A 43-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular in left arm on 10Jan2021 14:45 at single dose for COVID-19 immunization. Medical history included seasonal allergies, anxiety, depression, high cholesterol, tinnitus and GERD; all from an unknown date and unknown if ongoing. Concomitant medication included valaciclovir hydrochloride (VALTREX), omeprazole magnesium (PRILOSEC), iron, atorvastatin (LIPITOR), melatonin and BCP. The patient was previously vaccinated with first dose of BNT162B2 via unspecified route in left arm on 20Dec2020 15:00 for COVID-19 immunization and experienced vertigo/dizzy/room spins starting on 08Jan2021 23:30. The patient was not pregnant. The experienced vertigo/dizzy/room spins starting 1-2 days prior to 2nd vaccine 10Jan2021 then it was worsened in Jan2021 after 2nd vaccine. The patient experienced fatigue, sore body, HA (headache), nausea, racing thoughts and trouble sleeping in Jan2021. No treatment was given to the patient for the events. The outcome of the events was not recovered. The facility where the most recent COVID-19 vaccine was administered was in the hospital. 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 has not been tested for COVID-19. Information on the lot/batch number has been requested.

Other Meds: VALTREX; PRILOSEC [OMEPRAZOLE MAGNESIUM]; IRON; LIPITOR [ATORVASTATIN]; MELATONIN

Current Illness:

ID: 0980908
Sex: F
Age:
State:

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

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

Allergies:

Symptoms: Covid positive; Covid positive; This is a spontaneous report from a Pfizer-sponsored program Pfizer First Connect via a contactable consumer (patient). This reporter reported similar events for 2 patients (reporter and reporter's husband). This is 1st of 2 reports reported for the reporter. A female patient of an unspecified age received first dose of BNT162B2 via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient and her husband both had vaccine on Friday and they discovered that they both were Covid positive on Monday. Patient did not have symptoms but her husband did, the question was whether they should still get the second shot. Events outcome was unknown. Information on the Lot/Batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021049698 Same reporter, same drug, different patient

Other Meds:

Current Illness:

ID: 0980909
Sex: F
Age:
State: MD

Vax Date: 12/22/2020
Onset Date: 12/23/2020
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Continuous headache since first dose .; This is a spontaneous report from a contactable nurse (patient). A 53-years-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), unspecified route of administration on 22Dec2020 13:30 in right arm (at the age of 53-years-old) at SINGLE DOSE , second dose via an unspecified route of administration on 12Jan2021 16:30 in right arm (at the age of 53-years-old) at SINGLE DOSE for COVID-19 vaccination. Medical history included migraine from an unknown date and unknown if ongoing. The patient did not have any allergies. The patient's concomitant medications were not reported. The patient did not receive other vaccines in four weeks. The facility where the most recent COVID-19 vaccine was administered was at a hospital. Prior to the vaccination the patient was not diagnosed with COVID-19. Since the vaccination the patient had not been tested for COVID-19. On 23Dec2020, the patient experienced continuous headache since first dose. The patient did not receive treatment for the continuous headache since first dose. Outcome of the event continuous headache since first dose was not recovered.

Other Meds:

Current Illness:

ID: 0980910
Sex: F
Age:
State: MN

Vax Date: 01/14/2021
Onset Date: 01/15/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fever; Headache; body aches; Sore arm; This is a spontaneous report from a contactable healthcare professional (patient). A 41-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on 14Jan2021, at 18:30 as single dose for COVID-19 immunization. Medical history included hyperthyroidism and known allergy to latex. Concomitant medication included St. John's wort (MANUFACTURER UNKNOWN), elderberry (SAMBUCUS NIGRA), cetirizine hydrochloride (ZYRTEC). The patient experienced fever, headache, body aches and sore arm on 15Jan2021, at 04:30. No Covid prior vaccination was noted; the patient has not been tested for COVID post vaccination. No treatment was given for the events. The outcome of events was recovered in Jan2021. The batch/lot number for the vaccine, BNT162B2, was not provided and will be requested during follow-up.

Other Meds: ST JOHN'S WORT; ELDERBERRY [SAMBUCUS NIGRA]; ZYRTEC [CETIRIZINE HYDROCHLORIDE]

Current Illness:

ID: 0980911
Sex: F
Age:
State: CA

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

Lab Data:

Allergies:

Symptoms: bilateral eye irritation; edematous right eyelid since day of 2nd vaccine; This is a spontaneous report from a contactable nurse reported for herself. This 44-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), intramuscular at single dose in the left arm on 12Jan2021 10:15 for Covid-19 immunisation. The patient medical history was not reported. Concomitant medication included cetirizine hydrochloride (ZYRTEC [CETIRIZINE HYDROCHLORIDE]), paracetamol (TYLENOL). Previously the patient received the first dose of BNT162B2, intramuscular in the left arm on 24Dec2020 02:00 PM for Covid-19 immunisation. On 12Jan2021 12:00 PM, the patient experienced bilateral eye irritation, edematous right eyelid since day of 2nd vaccine. No treatment was performed. The outcome of the events was not recovered. The vaccine was administered at Hospital Facility. 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. The patient was not diagnosed with COVID-19 prior to vaccination. The patient had not been tested for COVID-19 post the vaccination. Information on the lot/batch number has been requested.

Other Meds: ZYRTEC [CETIRIZINE HYDROCHLORIDE]; TYLENOL

Current Illness:

ID: 0980912
Sex: F
Age:
State: MA

Vax Date: 01/15/2021
Onset Date: 01/16/2021
Rec V Date: 01/28/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Myalgias; dizziness; headache; fever; chills; This is a spontaneous report from a contactable Physician reporting for herself. A 50-years-old non-pregnant female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot EL1284), intramuscular in the left arm on 15Jan2021 15:00 at single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient previously received the first dose of bnt162b2 (lot SK5730) on 23Dec2020 at 09:30 AM intramuscular in left arm. The patient experienced myalgias, dizziness, headache, fever and chills on 16Jan2021 12:00 with outcome of recovered in Jan2021. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination the patient had not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 0980913
Sex: F
Age:
State: WA

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

Lab Data:

Allergies:

Symptoms: Nausea; Fatigue; Muscle/joint aches; Muscle/joint aches; Unusually sour taste in saliva in the mornings; This is a spontaneous report from a contactable consumer (patient). A 42-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: 3302), via an unspecified route of administration on 15Jan2021 07:30 in Left arm at single dose at Workplace clinic for COVID-19 immunisation. Medical history included Rhinosinusitis, Thoracic Outlet Syndrome, Polycystic ovarian syndrome (irregular menstrual cycles) and CBC issues: low white blood cell count, low lymphocyte count, high MCV (Mean cell volume) (under current care), all from an unknown date. Concomitant medication included Multivit, ergocalciferol (VIT D), folic acid (FOLIC), fish oil, magnesium, biotin. There was no other vaccine in four weeks. The patient did not have COVID prior vaccination and not had COVID tested post vaccination. The patient experienced Nausea, fatigue, muscle/joint aches and unusually sour taste in saliva in the mornings on 15Jan2021 11:00. The patient did not receive treatment for the events. The outcome of the events was recovering.

Other Meds: VIT D; FOLIC; FISH OIL; MAGNESIUM; BIOTIN

Current Illness: Lymphocyte count low; Mean cell volume high; White blood cell count low

ID: 0980914
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: weakness; confusion; dizziness; headache; hypotension; diarrhea; fatigue/lethargy; fatigue/lethargy; nausea; unilateral pain; photophobia x 3 days; Vomiting; This is a spontaneous report from a non-contactable Other HCP (patient). This 40-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, on 14Jan2021 at single dose for COVID-19 immunisation. Vaccine location was left arm. The patient was vaccinated at hospital, age at vaccination was 40-years-old. No other vaccine was received in four weeks. Medical history included migraines, IgM, and MGUS. Historical vaccine included first dose of BNT162B2 in left arm for COVID-19 immunisation. Concomitant medications included fremanezumab (AJOVY), escitalopram oxalate (LEXAPRO), and NURTEC (as reported). On 14Jan2021, the patient experienced vomiting, nausea, hypotension, weakness, unilateral pain and weakness, dizziness, confusion, headache, fatigue/lethargy, diarrhea, photophobia x 3 days. Events were recovering. No treatment was received for the event. No follow up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: AJOVY [FREMANEZUMAB]; LEXAPRO

Current Illness:

ID: 0980915
Sex: F
Age:
State: CA

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

Lab Data: Test Date: 20210114; Test Name: Fever; Result Unstructured Data: Test Result:100.2; Test Date: 20210115; Test Name: Fever; Result Unstructured Data: Test Result:99.8

Allergies:

Symptoms: swelling at injection site; pain, itching, redness, warmth at injection site; pain, itching, redness, warmth at injection site; pain, itching, redness, warmth at injection site; pain, itching, redness, warmth at injection site; body aches; fatigue; fever 100.2; This is a spontaneous report from a contactable Nurse. A 27-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# EL3249), intramuscular on 13Jan2021 10:45 at single dose for covid-19 immunisation. Vaccine location was left arm. Medical history included covid-19. Historical vaccine included first dose of BNT162B2 lot number EK5730 on 22Dec2020 10:15 AM. Concomitant medications included multivitamins, ascorbic acid (VITAMIN C), cetirizine hydrochloride (ZYRTEC). The patient experienced body aches on 14Jan2021 05:00, fatigue on 14Jan2021 05:00, fever 100.2 on 14Jan2021 05:00, pain, itching, redness, warmth at injection site on 15Jan2021. The patient underwent lab tests and procedures which included body temperature: 100.2 on 14Jan2021, and 99.8 on 15Jan2021. No treatment received. The events recovered in Jan2021.

Other Meds: MULTIVITAMINS [VITAMINS NOS]; VITAMIN C [ASCORBIC ACID]; ZYRTEC [CETIRIZINE HYDROCHLORIDE]

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm