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: 0939403
Sex: M
Age:
State:

Vax Date: 12/01/2020
Onset Date: 01/01/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data: Test Name: PCR test; Test Result: Negative

Allergies:

Symptoms: exposed to Covid positive patient; This is a spontaneous report from a contactable nurse (patient). A male patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: unknown), via an unspecified route of administration on Dec2020 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received his first dose of Covid19 vaccine on Dec2020 and was due for his second dose on 07Jan2021 (reported as today, day 21). However, his wife contracted Covid19 tested positive on 01Jan2021. He wanted to know when he should get his 2nd dose, having been exposed to Covid positive patient on Jan2021 and >21 days. His wife tested positive for Covid last Friday and he was on isolation/ negative on PCR. Outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0939404
Sex: F
Age:
State: WV

Vax Date: 12/21/2020
Onset Date: 01/06/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: muscle weakness on one side of her face; On 06Jan2021 I suddenly have tingling and muscle weakness on one side of my face.; This is a spontaneous report from a contactable other healthcare professional (patient). A 33-year-old female patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number=eh9899), intramuscularly on left arm at 07:15 AM on 21Dec2020 at single dose for COVID-19 immunization. Medical history included high blood pressure and asthma, no allergies to medications, food, or other products. Concomitant medication included lisinopril and non-hormone birth control. The patient suddenly had tingling and muscle weakness on one side of her face at 07:30 AM on 06Jan2021. All events were reported as non-serious. The patient did not receive any treatment from events. Prior to vaccination, the patient was not diagnosed with COVID-19; Since the vaccination, the patient had not been tested for COVID-19. The outcome of events was not recovered.

Other Meds:

Current Illness:

ID: 0939405
Sex: F
Age:
State:

Vax Date: 12/30/2020
Onset Date: 01/01/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: once by injection in the left shoulder/Shoulder pain; Whole body was hurting; Nausea; This is a spontaneous report from a contactable consumer (patient). A 36-year-old female patient received the first dose of bnt162b2 (PFIZER COVID 19 VACCINE, Batch/lot number: EL3246, expiry: unknown), via an unspecified route of administration on 30Dec2020 at single dose (once by injection in the left shoulder) for COVID-19 immunization (Healthcare worker). Medical history was reported as none. There were no concomitant medications. On 01Jan2021, it was reported that the patient experienced shoulder pain, whole body was hurting, and nausea. Patient asked, after getting the vaccine, if one was able to get COVID, she clarified that she meant after the first dose of the vaccine. She got the typical symptoms and side effects after she got the first dose, like shoulder pain. She is curious if you can still get COVID after the first dose. She is sure you are better off after the second one, but was curious about after the first one. The patient was taking COVID Vaccine because she is a Healthcare worker. Patient is a medical assistant. It was also reported that her shoulder pain was more prominent than her body. She works in the field and people are getting COVID after the first dose of the vaccine. She is concerned on if she could still get it or not. She gets the second dose on 20Jan2021. The outcome of the event once by injection in the left shoulder/Shoulder pain was recovered on 04Jan2021, whole body was hurting was recovered on 02Jan2021, and nausea was recovered on 01Jan2021.

Other Meds:

Current Illness:

ID: 0939406
Sex: M
Age:
State:

Vax Date: 12/01/2020
Onset Date: 12/01/2020
Rec V Date: 01/13/2021
Hospital:

Lab Data: Test Date: 202012; Test Name: heartrate; Result Unstructured Data: Test Result:rapid heartrate

Allergies:

Symptoms: rapid heart rate; trouble sleeping; This is a spontaneous report from a contactable healthcare professional. A 34-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number and expiry date: unknown), via an unspecified route of administration on the left deltoid on Dec2020 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient had the first vaccine approximately 2 weeks ago (Dec2020) and since then, patient have been having a rapid heart rate, especially at night time. He had trouble sleeping because it was beating fast. It was more pronounced the first week after vaccination on Dec2020. Patient will have a doctor's appointment on 08Jan2021. Outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0939407
Sex: F
Age:
State: FL

Vax Date: 12/18/2020
Onset Date: 12/18/2020
Rec V Date: 01/13/2021
Hospital:

Lab Data: Test Date: 20201218; Test Name: blood pressure; Result Unstructured Data: Test Result:went down drastically; Comments: 3mins post injection; Test Date: 20201218; Test Name: heartbeat; Result Unstructured Data: Test Result:Fast; Comments: 3mins post injection

Allergies:

Symptoms: feeling that I was going to pass out. faint; warm feeling starting on my right arm going down to my left leg/warm feeling from my right leg up to my heart; Fast heartbeat; headache; blood pressure went down drastically; tachycardia; weak; looked pale; Anxiety; This is a spontaneous report from a contactable Other HCP (patient). A 47-year-old female (not pregnant) patient received first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in right arm on 18Dec2020 10:00 at single dose for COVID-19 immunization. Facility where the most recent COVID-19 vaccine was administered was hospital. Medical history included patient was alergic to environmental or insect allergens. No food no medication''. Prior to vaccination, the patient was not diagnosed with COVID-19. Concomitant medication included loratadine. The patient receive other vaccines within 4 weeks prior to the COVID vaccine was immunotherapy vaccine against mold, insect, mites on 02Dec2020 on both arms. It was reported ''3mins post injection: warm feeling starting on my right arm going down to my left leg. feeling that I was going to pass out. faint. goes and come. I was feeling that I was going to pass out like 3 times , but I was in a wheelchair.. Thanks God and warm feeling from my right leg up to my heart. Fast heartbeat, and weak and sudden headache. Symptoms goes and come. it last 15 mins. Once I was brought to ER.. they estabilize my tachycardia and gave me benadryl. I did get better, but still weak. Stay 2 hours for observation. By the time I got to ER, I was a little better. Physician diagnoses as Anxiety event. because I got estabilize and never got a rash, difficulty breathing. I am 100%, my body for whatever reason it could be, did not welcome the vaccine. and blood pressure went down drastically...i looked pale as they told me.''. Adverse events start date was reported on 18Dec2020 10:03 AM. Case was non-serious. Treatment received for the adverse events included medicine for tachychardia and Benadryl. AE warm feeling starting on my right arm going down to my left leg/warm feeling from my right leg up to my heart and feeling that I was going to pass out. faint resulted in: [Emergency room/department or urgent care]. The outcome of the events ''warm feeling starting on my right arm going down to my left leg/warm feeling from my right leg up to my heart'' and ''feeling that I was going to pass out. faint'' was reported as recovered. The outcome of other events was unknown. Information about Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0939408
Sex: F
Age:
State: KS

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

Lab Data: Test Name: COVID; Test Result: Negative ; Test Name: strep throat; Test Result: Negative

Allergies:

Symptoms: Sore throat- swollen on the outside; Sore throat- swollen on the outside; Lymph nodes; This is a spontaneous report from a contactable pharmacist. A 49-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/expiry: 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. The patient previously took Taltz for psoriasis (pending clarification). It was reported that "day after HA etc" on an unspecified date; sore throat- swollen on the outside. "Lymph nodes?" was also reported. It was reported that the patient still sore (sore throat) and tested negative for COVID and strep throat. "Psoriasis TALTs med? - Second dose?" was also stated. For their vaccine storage, it was reported that the state sent them. It had to be used within 5 days after removal - and stored under refrigeration, asking if it can be extended for at least a day would be helpful. The pharmacist was asking for extended stability of thawed vials in the refrigerator. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0939409
Sex: M
Age:
State: MI

Vax Date: 12/22/2020
Onset Date: 01/06/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: I am nursing. My son (7 months old) developed a rash and fussiness. No fever. I do not have any symptoms myself.; rash; fussiness; This is a spontaneous report from a contactable physician. This physician reported events for 2 patients (herself and baby). This is the baby report. A 7-month old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1685, expiry date not reported), transmammary on 22Dec2020 14:30 at a single dose for COVID-19 immunisation. Medical history was none. Concomitant medication included levothyroxine. The patient's mother reported that "I am nursing. My son (7 months old) developed a rash and fussiness. No fever. I do not have any symptoms myself". The events started from 06Jan2021. Patient's mother had no COVID prior vaccination. No COVID tested post vaccination. The event was assessed non-serious. Facility where the most recent COVID-19 vaccine was administered was hospital. The patient's mother did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No treatment was received for the adverse event. Prior to vaccination, the patient's mother was not diagnosed with COVID-19. Since the vaccination, the patient's mother had not been tested for COVID-19. Clinical outcome of the events was not recovered.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021007817 mother/baby case

Other Meds:

Current Illness:

ID: 0939410
Sex: F
Age:
State: TX

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

Lab Data: Test Date: 20210104; Test Name: Fever; Result Unstructured Data: Test Result:above 101; Test Date: 20210104; Test Name: tachycardia; Result Unstructured Data: Test Result:140 bpm; Comments: 140 bpm

Allergies:

Symptoms: tachycardia (140 bpm); Fever above 101; myalgia; joint pain right arm, joint pain and swelling to right wrist; joint pain and swelling to right wrist; swollen lymph node on right side of body; weakness; skin redness and burning sensation; skin redness and burning sensation; tremors; gum pain; fatigue; migraine; sweating; back pain; first dose of bnt162b2 on 18Dec2020 at 16:00, second dose on 04Jan2021 at 08:00 AM; This is a spontaneous report from a contactable nurse (patient). A 32-year-old female patient (not pregnant) received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: ELU140), via an unspecified route of administration on 04Jan2021 at 08:00 AM on Right arm at single dose for COVID-19 immunization. The patient medical history included had known allergies with Penicillin, bees and wasp. Prior to vaccination, patient was not diagnosed with COVID-19. Concomitant medications included colecalciferol, retinol (VITAMIN A); colecalciferol (VITAMIN D); calcium phosphate dibasic, phytomenadione (VITAMIN K); cyanocobalamin (VITAMIN B12); levothyroxine, liothyronine (NP THYROID). Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: ELO140), via an unspecified route of administration on 18Dec2020 at 16:00 on Right arm at single dose for COVID-19 immunization. The patient experienced fever above 101, tachycardia (140 bpm), myalgia, joint pain right arm, joint pain and swelling to right wrist, swollen lymph node on right side of body, weakness, skin redness and burning sensation, tremors, gum pain, migraine, fatigue, sweating and back pain, all on 04Jan2021 at 20:00, events were resulted in doctor or other healthcare professional office/clinic visit. Since the vaccination, patient had not been tested for COVID-19. It was unknown if any treatment was received for events. The outcome of the events was not recovered. The report was reported as non-serious, with seriousness criteria-Results in death: No; Life threatening: No; Caused/prolonged hospitalization: No; Disabling/Incapacitating: No; Congenital anomaly/birth defect: No.

Other Meds: NP THYROID; VITAMIN A [COLECALCIFEROL;RETINOL]; VITAMIN D [COLECALCIFEROL]; VITAMIN K [CALCIUM PHOSPHATE DIBASIC;PHYTOMENADIONE]; VITAMIN B12 [CYANOCOBALAMIN]

Current Illness:

ID: 0939411
Sex: F
Age:
State:

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

Lab Data: Test Date: 20210104; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptoms: muscle and joint pains that got progressively worse over the next 24 hours; muscle and joint pains that got progressively worse over the next 24 hours; body pain/body aches; I also have shaking chills; throbbing headache; tender anterior cervical lymphadenopathy; runny nose; dry cough; chest tightness; First dose of bnt162b2 on 18Dec2020/ second dose on 04Jan2021; This is a spontaneous report from a contactable physician (patient). A 27-year-old female patient (pregnant: No) received of bnt162b2 (Pfizer), via an unspecified route of administration in left arm on 04Jan2021 07:15 at single dose (second dose), via an unspecified route of administration in left arm on 18Dec2020 12:30 at single dose (first dose dose) for COVID-19 immunization. Medical history included asthma, allergies from an unknown date and unknown if ongoing. Allergies to medications, food, or other products was none. The patient's concomitant medications were not reported. Around 12 hours after the second dose, the patient started feeling muscle and joint pains that got progressively worse over the next 24 hours. She had to miss 1 work day so far due to body pain despite alternating taking ibuprofen and paracetamol (APAP) around the clock. It was now 48 hours after the vaccine, and she still have severe body aches. She also had shaking chills, throbbing headache, tender anterior cervical lymphadenopathy, runny nose, dry cough and chest tightness. Of note, she was a healthcare worker and tested negative for COVID PCR immediately after she received my second dose of the vaccine. She was tested due to a low-suspicion possible workplace exposure 5 days prior. She had no symptoms before the vaccine. The patient underwent lab tests and procedures which included nasal swab test: negative on 04Jan2021. The events were reported as non-serious. The adverse event didn't result in emergency room visit or physician office visit. No treatment received for the adverse event. Facility where the most recent COVID-19 vaccine was administered: Workplace clinic. The patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. List of any other medications the patient received within 2 weeks of vaccination: Birth control pills. Prior to vaccination, the patient wasn't diagnosed with COVID-19. Since the vaccination, the had patient been tested for COVID-19. The outcome of events was resolving. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0939412
Sex: F
Age:
State: OK

Vax Date: 01/04/2021
Onset Date: 01/07/2020
Rec V Date: 01/13/2021
Hospital:

Lab Data: Test Date: 20210105; Test Name: fever of; Result Unstructured Data: Test Result:100.7

Allergies:

Symptoms: dizziness; nausea; joint pain; itching and broke out in rash around injection site; itching and broke out in rash around injection site; pain and stinging on injection site location; heat and redness as well as a raised rash; heat and redness as well as a raised rash; Both ears got, rot and itchy, stomach itchy; Both ears got, rot and itchy, stomach itchy; fever of 100.7; sever heart burn; severe body aches; head ache; raised rash; This is a spontaneous report from a contactable other Health Care Professional (HCP) who is the patient. A 28-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number unknown, expiration date unknown) via an unspecified route of administration on 04Jan2021 at 10:00 AM (at the age of 28-years-old) at an unspecified dose in the right arm for COVID-19 vaccination. Medical history included removal of a metastatic carcinoid tumor from an unknown date and unknown if ongoing. The patient's allergies include minor hive breakouts from "several things." The patient's historical vaccinations included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number unknown) via an unspecified route of administration on 17-DEC-2020 at 14:00 (at the age of 27-years-old) at an unspecified dose in the right arm. The patient was not pregnant at the time of this vaccination. The patient was administered the vaccine in the hospital. Prior to this vaccination, the patient was not diagnosed with COVID-19. Concomitant medication included drospirenone;ethinylestradiol;levomefolic acid (reported as "generic form of Beyaz") and acetaminophen.The patient did not receive any other vaccines within four weeks prior to the first vaccination. On 04Jan2021 at 10:00 PM the patient experienced severe body aches and head ache, through out that night. She had dizziness and nausea with increased joint pain and body aches with the head ache increasing as well. On the morning of 05Jan2021 she experienced a fever of 100.7 and body aches. On that same day in the afternoon these symptoms subsided. She also experienced severe heart burn on 05Jan2021 that did not subside with Tums. On Wednesday 06Jan2021 she was feeling much better, and she had a "normal day." At 12:00 AM on 07Jan2021 the patient started itching and broke out in a rash around the vaccination site, and pain and stinging at injection site. She also had heat and redness as well as a raised rash. Both ears got, hot and itchy, her stomach was itchy but not red or swollen, same for the right leg and foot. She took one allergy pill, and twenty minutes later was still having a bad reaction so she took another allergy pill. She stayed awake to fill out this form, and she was hoping the reaction would stop spreading. Treatment was reported as having taken Tums for the severe heart burn and the patient also took an unspecified "allergy pill" for the itching, vaccination site rash, pain and stinging, the heat, redness and raised rash, the red, hot itchy ears, and the itchy stomach. The clinical outcome of the events severe body aches and fever was reported as recovered on 05Jan2020. The clinical outcome of headache, dizziness, nausea, joint pain, heartburn, vaccination site rash, vaccination site pruritus, vaccination site pain, feeling hot, redness, itchy, ear disorder and raised rash was reported as recovering. It was also reported that since the vaccination the patient had not been tested for COVID-19. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds: ; ACETAMINOPHEN

Current Illness:

ID: 0939413
Sex: F
Age:
State: KS

Vax Date:
Onset Date: 01/07/2021
Rec V Date: 01/13/2021
Hospital:

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

Allergies:

Symptoms: lower back cramps; This is a spontaneous report from a contactable healthcare professional. A 19-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration at the left arm on an unspecified date at a single dose for COVID-19 immunization at a nursing home/senior living facility. The patient's medical history and concomitant medications were not reported. The patient was not pregnant. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at the right arm on 17Dec2020 for COVID-19 immunization. The patient experienced lower back cramps on 07Jan2021 and was treated with ibuprofen. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient been tested for COVID-19? since vaccination and was negative via a nasal swab on 06Jan2021. The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was recovering from the event. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0939414
Sex: F
Age:
State: WA

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

Lab Data:

Allergies:

Symptoms: fatigue; patient received the second dose in less than 21 days from the first dose; tenderness in the arm; This is a spontaneous report from contactable nurse, the patient. A 58-year-old non-pregnant female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EK5730), via an unspecified route of administration in the left arm on 04Jan2021 (at the age of 58-years-old) as a single dose for COVID-19 immunization. Medical history included hypothyroidism, depression, and asthma. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included levothyroxine (MANUFACTURER UNKNOWN), montelukast sodium (SINGULAIR), bupropion hydrochloride (WELLBUTRIN), vitamin B complex (MANUFACTURER UNKNOWN), magnesium (MANUFACTURER UNKNOWN), vitamin D3 (MANUFACTURER UNKNOWN), ascorbic acid (VIT C), and multivitamins (MANUFACTURER UNKNOWN). The patient previously received the first dose of BNT162B2 on 17Dec2020 at 08:00 (Lot Number: EK5730; at the age of 58-years-old) for COVID-19 immunization in the left arm and experienced severe arm pain. The patient did not receive any other vaccines within four weeks prior to the second vaccination (except the first vaccination). On 04Jan2021, the patient had tenderness in the arm. The patient took acetaminophen (MANUFACTURER UNKNOWN) which helped. On 05Jan2021, the patient experienced fatigue. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcomes of the tenderness in the arm and fatigue were recovered on unknown dates in Jan2021.

Other Meds: ; SINGULAIR; WELLBUTRIN; ; ; VITAMIN D3; VIT C

Current Illness:

ID: 0939415
Sex: M
Age:
State: MA

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: chills; headache; feeling tired; This is a spontaneous report from a contactable other healthcare professional (patient). A 29-year old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number EK9231 and expiry date unknown) intramuscular at left arm on 06Jan2021 08:00 at single dose for Covid-19 immunization in a hospital facility. Medical history was none. The patient previously took cephalexin and experienced allergies. Historical vaccines included first dose of BNT162B2 (lot number EH9899) on 16Dec2020 08:00 (29 years old) and was administered in a hospital facility intramuscularly at the left arm; the patient did not receive any other vaccines in four weeks prior to Covid-19 vaccination and has no Covid prior to the vaccination. On 06Jan2021 21:00 several hours after taking the second vaccine, the patient developed chills, headache, and was feeling tired. The patient was not Covid tested post vaccination. The patient did not received treatment due to the events. The outcome of the events chills, headache, and feeling tired was recovering. The reporter considered the events non-serious; did not result in death, was not life threatening, did not caused/prolonged hospitalization, was not disabling/incapacitating, and no congenital anomaly/birth defect.

Other Meds:

Current Illness:

ID: 0939416
Sex: F
Age:
State:

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

Lab Data: Test Date: 202101; Test Name: tested for COVID-19; Result Unstructured Data: Test Result:results unknown

Allergies:

Symptoms: Fever; headache; body aches; This is a spontaneous report from a non-contactable other healthcare professional reporting for herself. A 34-year-old female patient started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot number EK9231), via an unspecified route of administration on 05Jan2021 14:00 at single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19 (results unknown). The patient experienced fever, headache, body aches an unspecified date in Jan2021. Event outcome was unknown. The reporter assessed the events as non-serious. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0939417
Sex: F
Age:
State: MD

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: metallic taste in my mouth; This is a spontaneous report from a contactable nurse (patient). A 61-year-old female patient received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; lot number: EL1284; expiration date: not known), via an unspecified route of administration on right arm on 06Jan2021 07:15 at single dose for covid-19 immunization, administered at hospital. Medical history included pacemaker for bradycardia w/syncopal episodes; and allergy to poppy seeds and pineapple. The patient is not pregnant at the time of vaccination. Concomitant medications included rosuvastatin calcium (CRESTOR), colecalciferol (VIT D3), and an unspecified multivitamin (other medications received within two weeks of vaccination). No other vaccines received within four weeks prior to covid vaccine. The patient previously took morphine and experienced drug allergy. The patient was not diagnosed with covid-19 prior to vaccination and had not been tested with covid-19 since the vaccination. The patient experienced metallic taste in her mouth approximately one minute after receiving the vaccine on 06Jan2021 07:15; it lingered for about six hours (13:15). The event was reported non-serious. The patient did not receive treatment for this event. The outcome of the event was recovered on 06Jan2021 13:15.

Other Meds: CRESTOR; VIT D3

Current Illness:

ID: 0939418
Sex: F
Age:
State: MI

Vax Date: 01/04/2021
Onset Date: 01/05/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: I've felt like I have the flu for the past 3 days; aches/pains; sore throat; sinus pressure; extreme fatigue; sleeping most of the day making it hard to work; feeling worse, not better; fogginess; This is a spontaneous report from a contactable Other-HCP (patient herself). This 31-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number EK9231), via an unknown route, on 04Jan2021 at 08:00 at 0.3 ml single for COVID-19 immunisation. The patient was not pregnant. Vaccine location was left arm. Relevant medical history included depression, anxiety, endometriosis. No known allergies. Relevant concomitant medications included bupropion hydrochloride (WELLBUTRIN), escitalopram oxalate (LEXAPRO), and colecalciferol (VITAMIN D). The patient was vaccinated at Workplace clinic, age at vaccination was 31-year-old. No other vaccine was received in four weeks. Pre-vaccination and post-vaccination COVID tests were not performed. The patient stated that on 05Jan2021 ''I've felt like I have the flu for the past 3 days-aches/pains, sore throat, sinus pressure, fogginess, extreme fatigue; I'm sleeping most of the day making it hard to work; feeling worse, not better, each day; trying OTC meds- loratadine pseudoephedrine sulfate (CLARITIN D) and chlorphenamine maleate, paracetamol, pseudoephedrine hydrochloride (TYLENOL COLD); plan to call doctor if not feeling better by day 5''. The patient had not recovered from the events. No follow-up attempts are possible. No further information is expected.

Other Meds: WELLBUTRIN; LEXAPRO; VITAMIN D [COLECALCIFEROL]

Current Illness:

ID: 0939419
Sex: F
Age:
State: SC

Vax Date: 01/06/2021
Onset Date: 01/07/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: aches/pains shooting down my right leg; severe lower back pain; This is a spontaneous report from a contactable nurse. This 54- year-old female patient (reported for herself) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Lot number: lot EK5730), via an Intramuscular route of administration, on 06Jan2021 at 09:00 AM (at the age of 54-years-old) as a single dose for COVID-19 vaccination. The facility where COVID-19 vaccine was administered was at a hospital and anatomically located on the right arm. The patient reported allergies to food. The patient does not have any medical history. Concomitant medication included omeprazole ((MANUFACTURER UNKNOWN) 20 mg QD, diclofenac (MANUFACTURER UNKNOWN) 75 mg EC tablet QD. The patient was not pregnant at the time of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 07Jan2021 3:00AM, 18 hours after 1st dose, she experienced severe lower back pain with aches/pains shooting down my right leg. Nine hours, after the injection I took 1 gm of Tylenol. At 3 am, I took another 1 gm of Tylenol with some relief. At 8 am took 400 mg of Motrin with some relief-aches/pain still there. No paralysis or weakness. The patient received Tylenol and Motrin as treatment for the events. The clinical outcome of the events aches/pains shooting down my right leg and severe lower back pain was not recovered. Patient was not tested for COVID-19 since having the vaccine. No follow-up attempts are possible. No further information is expected.

Other Meds: ;

Current Illness:

ID: 0939420
Sex: F
Age:
State: AR

Vax Date: 01/06/2021
Onset Date: 01/07/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chills; Low grade fever; Nausea; Pain; Swollen lymph nodes in armpit; This is a spontaneous report from a contactable Healthcare Professional (patient).This 42- year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Lot number: lot EL3246), via an Intramuscular route of administration, on 06Jan2021 09:15AM (at the age of 42-years-old) as a single dose for COVID-19 vaccination. The facility where COVID-19 vaccine was administered was at a hospital and anatomically located on the left arm. The patient did not have any allergies to medications, food, or other products. Medical history included: Mitral valve prolapse. Concomitant medications were not reported. The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Lot number: lot EH9899) via an Intramuscular route of administration, on 18Dec2020 at 03:30 PM (at the age of 42-years-old) as a single dose for COVID-19 vaccination, anatomically located on the right arm. The patient was not pregnant at the time of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 07Jan2021 at 01:30 AM, she experienced chills, low grade fever, nausea, pain, and swollen lymph nodes in armpit. The patient did not receive treatment for the events. The clinical outcome of the events chills, low grade fever, nausea, pain, and swollen lymph nodes in armpit was recovering. It was also reported that since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0939421
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: fatigue; Pain in injection site; headache; diaphoretic; nauseous; felt like I was gong to pass out; dry heaves; ringing in my ears; vision changes; unwellness; This is a spontaneous report from a Non-contactable nurse, the patient. A 33 (units unknown) adult female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration on an unknown date 11:15 as a single dose for Covid-19 immunization. Medical history and concomitant medications were not reported. On an unknown date, the patient experienced pain in injection site which began later in the evening, a little soreness only and a little bit of a headache; and fatigue and feeling unwell. The next morning the patient experienced feeling diaphoretic, nauseous, felt like she was going to pass out, vision changes, ringing in ears and dry heaves. It was reported she was doing every she could do to keep consciousness and did not feel better until she had the dry heaves. The clinical outcome of the events visual changes, ringing in the ears and dry heaves was recovered; fatigue and unwellness was not recovered; vaccination site pain, headache, diaphoretic, nauseous, and dizziness was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 0939422
Sex: F
Age:
State: IN

Vax Date: 01/05/2021
Onset Date: 01/06/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: headache; muscle pain; chills; fever; injection site redness and swelling; injection site redness and swelling; Injections site pain; tiredness; This is a spontaneous report from a contactable nurse (patient herself). A 54-year-old female patient (non-pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# EK5730), via intramuscular on 05Jan2021 10:30 in left arm at single dose for covid-19 immunization. Medical history included hypothyroidism, arthritis, hypertension, eczema. Prior to vaccination, the patient was diagnosed with COVID-19. The patient was known allergies: daptomycin and cefdinir (OMNICEF). The most recent COVID-19 vaccine was administered was in hospital. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Other medications the patient received within 2 weeks of vaccination included clonidine, levothyroxine sodium (SYNTHYROID), ibuprofen. The patient experienced injections site pain, tiredness, headache, muscle pain, chills, fever, injection site redness and swelling on 06Jan2021 11:00 with outcome of recovering. Since the vaccination, the patient had not been tested for COVID-19. No treatment received for the adverse event. Events were reported as non-serious.

Other Meds: ; SYNTHYROID;

Current Illness:

ID: 0939423
Sex: M
Age:
State: FL

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: slight headache; Sore arm; 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; Solution for injection, Lot number: EH9899, unknown expiration), intramuscularly on left arm, on 06Jan2021 at 09:00, at single dose, for COVID-19 immunization. Medical history included penicillin allergy. Concomitant medications included acetylsalicylic acid (BABY ASPIRIN), fenofibrate (FENOFIBRATE), atorvastatin, and indapamide (INDAPAMID). On 06Jan2021 at 10:00 AM, the patient experienced sore arm and slight headache that last one day (07Jan2021). The patient was not diagnosed with COVID-19 prior to vaccination and has not been tested for COVID post vaccination. No treatment was received for the events. It was unknown if the patient received any other vaccines within 4 weeks prior to COVID vaccine. The patient recovered from the events on 07Jan2021. The events were assessed as non-serious.

Other Meds: BABY ASPIRIN; ; ; INDAPAMID

Current Illness:

ID: 0939424
Sex: M
Age:
State: PA

Vax Date: 01/05/2021
Onset Date: 01/06/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data: Test Name: I had body chills fever 103; Result Unstructured Data: Test Result:103

Allergies:

Symptoms: I had body chills fever 103 degree Celsius; body aches; Diarrhea; migraine headache; shivering; This is a spontaneous report from a contactable health care professional, the patient. A 31-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number EK9231) intramuscular in the left arm on 05Jan2021 at 5:30 PM (at the age of 31-year-old) as a single dose for COVID-19 immunization. The patient medical history was not reported. The patient did not have any allergies to medications, food, or other products. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient's concomitant medications were not reported. Historical vaccine included Dose 1 of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number EK5730), intramuscular, left arm on 17Dec2020 for COVID-19 immunization. On 06Jan2021 at 05:00 AM, the patient experienced body chills fever (103 degree Celsius), body aches, diarrhea, migraine headache, shivering. The events was reported as non-serious. The patient underwent lab test which included body temperature: 103 degree Celsius. The patient did not receive any treatment for the body chills fever (103 degree Celsius), body aches, diarrhea, migraine headache, shivering. The clinical outcome of the events body chills fever (103 degree Celsius), body aches, diarrhea, migraine headache, shivering was recovering. It was also reported that since the vaccination, the patient had not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 0939425
Sex: M
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: Has been itching like crazy/rash/ super itchy at night; This contactable physician reported similar events for two patients. This is the 2nd of two reports (guy he works with). A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot/batch number: EH9899), via an unspecified route of administration and date at SINGLE DOSE for COVID-19 immunization. Medical history and concomitant medications were not reported. The physician also stated that the patient which the reporter worked with had something similar event experienced (AER 2021008113). It was elaborated that the patient had rash and it was super itchy at night noted on an unknown date. The patient received the same lot number and has been itching like crazy. They have both been trying to figure out what to do. It was clear as mud. Then, last week (Jan2021) they saw each other, and they were both having the same issue and suffering separately. They had no exposure to anything similar besides the vaccine. The patient did a steroid pack, which his itchiness went away and got better while he was on it. When he stopped it, the itchiness came back. It reminds him when he got poison ivy in medical school. It was the same scenario. It holds off on steroids, then comes back after you are no longer taking them. He said that the antihistamine he took, and the steroid cream did not help. He took brand new loratadine (CLARITIN) which was same for the cream. He used multiple tubes of cream and applied it twice a day. It says you could use it up to 6 times a day, which he was working so would use twice a day. If he was not working, he would apply it more. The outcome the event was not recovered.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021008113 same reporter/drug, similar events, different patient

Other Meds:

Current Illness:

ID: 0939426
Sex: M
Age:
State: TX

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

Lab Data:

Allergies:

Symptoms: Nausea; vomiting; Fever with chills; Myalgias; Upper respiratory tract congestion; Injection site pain; patient received the second dose of BNT162B2 on 05Jan2021; This is a spontaneous report from a contactable physician (patient himself). A 25-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# EL3248), via intramuscular on 05Jan2021 13:00 in left arm at single dose for covid-19 immunization. Medical history included none. Allergies to medications, food, or other products was no. The patient's concomitant medications were not reported. The patient previously took the first dose of BNT162B2 on 18Dec2020 10:00 for covid-19 immunization. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The most recent COVID-19 vaccine was administered was in hospital. The patient experienced nausea, vomiting, fever with chills, myalgias, upper respiratory tract congestion and injection site pain, all on 06Jan2021 03:00 with outcome of not recovered. Treatment of paracetamol (TYLENOL) was received for the events. All events were reported as non-serious.

Other Meds:

Current Illness:

ID: 0939427
Sex: M
Age:
State: AL

Vax Date: 01/06/2021
Onset Date: 01/07/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chills; Fever; This is a spontaneous report from a contactable consumer (patient). A 53-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot/batch number: EK5730, expiry: 31Mar2021), intramuscular on the left arm on 06Jan2021 13:00 at SINGLE DOSE for COVID-19 immunization It was reported that the patient was visiting COVID-19 patients. There were no concomitant medications. The patient previously received the first dose of PFIZER-BIONTECH COVID-19 VACCINE (lot/batch number: EK5730, expiry: 31Mar2021) intramuscular on the left arm on 16Dec2020 as COVID-19 immunization. The patient reported that he received the second dose of the Pfizer BioNTech COVID-19 vaccine yesterday (06Jan2021) and was having a minor reaction. He has chills and fever and fever this morning (07Jan2021) and wanted to know if it's okay to take over the counter ibuprofen or acetaminophen (TYLENOL). Outcome of the events were not recovered.

Other Meds:

Current Illness:

ID: 0939428
Sex: M
Age:
State: TN

Vax Date: 01/06/2021
Onset Date: 01/01/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: fatigue; threw up a little; patient received the second dose of BNT162B2 on 06Jan2021; soreness in his right arm/soreness in his legs/legs were hurting; did not sleep good; sick to his stomach; This is a spontaneous report from a contactable consumer (patient himself). A 58-year-old male patient the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# EL0140), via intramuscular on 06Jan2021 15:00 in right arm at 0.3 mL (30mcg), single for preventative. There were no medical history and concomitant medications. Patient had the first dose of BNT162B2 vaccine on 19Dec2020 for covid-19 immunization. No investigation assessment was received. Patient had the second Pfizer COVID19 vaccine shot yesterday around 15:00 on 06Jan2021. He was asking if it was normal to be sore, patient had a little fatigue on 07Jan2021 and be sick to his stomach in Jan2021. The soreness in his right arm started last night (06Jan2021). He experienced soreness in his legs. He did not sleep good and his legs were hurting last night through the night. As of now his legs do not seem as bad. Patient went to work this morning and then he left work to go back home. He ate a cake and milk before he left for work. He threw up a little on 07Jan2021. It did not take much for him to gag, he even gags when brushing his teeth. Right now and within the last hour, he had not felt sick to his stomach. Outcome of soreness in his right arm/soreness in his legs/legs were hurting was not recovered, of fatigue was recovering, of sick to his stomach was recovered on 07Jan2021, of other events was unknown.

Other Meds:

Current Illness:

ID: 0939429
Sex: F
Age:
State: MN

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

Lab Data: Test Date: 20210105; Test Name: low-grade fever; Result Unstructured Data: Test Result: highest it has been 99.5

Allergies:

Symptoms: I have had a sore arm; I also have been having a low-grade fever the highest it has been 99.5; Body aches; Chills; This is a spontaneous report from a contactable nurse reporting for self. A 36-years-old female patient started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), Lot# EK923, via an unspecified route of administration on 05Jan2021 08:45 as a single dose (dose 1), left arm (age at vaccination: 36 years old), for COVID-19 immunization. The patient was not pregnant at the time of vaccination. There was no other vaccine administered in the 4 weeks prior to the COVID vaccine. Medical history included multiple sclerosis and hypothyroidism . The patient was receiving unspecified concomitant medications ("10 meds").The patient previously took copaxone and experienced drug allergy. The patient reported having a sore arm, but also had been having a low-grade fever. The highest it had been was 99.5. The patient also had body aches and chills. These symptoms started couple hours after the injection (on 05Jan2021) and have been with the patient since then. The events were reported as non-serious. There was no hospitalization or treatment received for the events. The outcome of the events sore arm, low grade fever, body aches, and chills was not recovered. The patient had not been COVID-19 tested post vaccination.

Other Meds:

Current Illness:

ID: 0939430
Sex: F
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: Arm pain; Nausea; lightheadedness; This is a spontaneous report from a contactable healthcare professional (patient). A 64-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot/batch number: not provided), via an unspecified route of administration on the left arm in Jan2021 at SINGLE DOSE for COVID-19 immunization at the hospital. Medical history included hypothyroidism. It was reported that the patient had allergies with sulfa and trimethoprim / sulfamethoxazole (BACTRIM). Concomitant medications included levothyroxine sodium (SYNTHYROID), ergocalciferol (VIT D), levocetirizine dihydrochloride (XYZAL). It was stated that the patient was not diagnosed with COVID-19 prior to vaccination and has not been tested for COVID-19 since the vaccination. In Jan2021, the patient experienced arm pain after 10 hours of getting the vaccine. It was also reported that nausea and lightheadedness the following day. No treatment received for the adverse events. The patient recovered from the events in Jan2021 (reported as feeling passed after 2hrs) Information on the lot/batch number has been requested.

Other Meds: SYNTHYROID; VIT D; XYZAL

Current Illness:

ID: 0939431
Sex: M
Age:
State: PA

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fever; Chills/Shivering; Muscle Aches and Soreness; Fatigue; This is a spontaneous report from a contactable other healthcare professional (patient). A 37-year-old male patient received 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231), via an unspecified route of administration in right arm on 06Jan2021 08:45 at single dose for Covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient previously took bupropion hydrochloride (WELLBUTRIN) and clindamycin, both experienced drug allergy, previously received 1st dose of BNT162B2 in right arm in Dec2020 at 08:45 AM for covid-19 immunisation. No other vaccine in four weeks. No covid prior vaccination. The patient experienced fever, chills, shivering, muscle aches and soreness, fatigue on 06Jan2021 22:00. No treatment received for events. The outcome of events was recovering. The case was reported as non-serious. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had bot been tested for COVID-19.

Other Meds:

Current Illness:

ID: 0939432
Sex: F
Age:
State: DC

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

Lab Data:

Allergies:

Symptoms: Headache; Unexplainable crying/emotional; Unexplainable crying/emotional; Awful R shoulder pain; This is a spontaneous report from a contactable other HCP (patient). A 28-year-old female patient received the first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number: EK9231), via an unspecified route of administration on 05Jan2021 at 12:45 at single dose in right arm for covid-19 immunization. Medical history included acute lymphoblastic leukemia at age 11, remission for 14 years. The patient's concomitant medications were not reported. The patient previously took sulfamethoxazole trimethoprim (BACTRIM) and experienced allergies. The patient experienced headache, unexplainable crying/emotional, awful right shoulder pain; all on 05Jan2021 at 15:30. All events were reported as non-serious. The patient did not receive treatment for the events. 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, and the patient has not been tested for COVID-19 since the vaccination. The outcome of the events was resolved in Jan2021.

Other Meds:

Current Illness:

ID: 0939433
Sex: M
Age:
State: FL

Vax Date: 01/04/2021
Onset Date: 01/05/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: fever; Result Unstructured Data: Test Result:99.5

Allergies:

Symptoms: swelling of the lymph nodes; fever; right arm injection site pain; aches and pains; chills; This is a spontaneous report from a Pfizer-sponsored program via a contactable consumer (patient). A 53-year-old male patient received the first dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/lot number: EL0140), intramuscular on 04Jan2021 at 13:00 at single dose in right shoulder for covid-19 prophylaxis. There were no medical history or concomitant medications. The patient experienced fever, right arm injection site pain, aches and pains, and chills on 05Jan2021, swelling of the lymph nodes on 06Jan2021. Event details: On 05Jan2021 in the morning, he started having a fever and chills. He stated that he noticed the injection site pain on the 05Jan2021 and stated that it only hurt at time of reporting if he pushed on it. He stated it did not hurt when he moved his arm around. The patient stated that he noticed the aches and pains on the 05Jan2021 in the morning and it stuck with him throughout the day and was over by the time he went to bed on 05Jan2021. Wednesday 06Jan2021, toward the early morning around 0300 under his arm hurt and the lymph node under his arm was swollen about the size of a baseball. The patient said that his fever was currently 99.5 in Jan2021. The outcome of events fever and swelling of the lymph nodes was not resolved, outcome of right arm injection site pain, aches and pains was resolved in Jan2021, outcome of event chills was unknown.

Other Meds:

Current Illness:

ID: 0939434
Sex: F
Age:
State: AL

Vax Date: 01/06/2021
Onset Date: 01/07/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data: Test Date: 20210107; Test Name: Temperature; Result Unstructured Data: Test Result:101.2 Fahrenheit; Test Date: 20210107; Test Name: Temperature; Result Unstructured Data: Test Result:100.5 Fahrenheit

Allergies:

Symptoms: Temperature was 101.2F/100.5 degrees Fahrenheit; Felt fatigue; Congestion; Headache; felt warm; This is a spontaneous report from a contactable nurse (patient). A 23-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899), second dose via an unspecified route of administration on 06Jan2021 at a single dose for COVID-19 immunization (direct patient care). The patient previously took first dose of bnt162b2 via an unspecified route of administration on 16Dec2020 at a single dose in the right deltoid for COVID-19 immunization and she had no side effects to. There were no medical history or concomitant medications. On 07Jan2021, the patient experienced temperature was 101.2 degrees Fahrenheit, felt fatigue, congestion and headache. She woke up this morning an felt warm, which was why she took her temperature. She also took paracetamol (TYLENOL) last night prior to bed but clarifies that she had no side effects last night from the COVID Vaccine. They all started this morning. Treatment included after she checked her temperature, she took 1000 mg of paracetamol. She rechecked her temperature 1.5 hours later and it was 100.5 degrees Fahrenheit. The paracetamol also helped her headache improve. The outcome of event temperature was 101.2F and headache and felt warm was recovering, outcome of events not recovered. Relatedness of product to reactions temperature of 101.2 degrees Fahrenheit, fatigue, Congestion, Headache was assessed related by Primary Source Reporter. Events temperature of 101.2 degrees Fahrenheit and congestion were assessed related to COVID vaccine. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0939435
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Headache; This is a spontaneous report from a contactable consumer reporting for herself. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) lot number was not reported, via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient mentioned that she was still having side effects. She got the vaccine a week ago, on Saturday (unspecified date), and she was still having side effects. She wanted to know how long the side effects are going to last for "like what's the longest you have seen." It was clarified that she had the vaccine 9-10 days ago (unspecified date) and she had a headache ever since that doesn't go away. She asked is she should still get the second dose if she was still having symptoms of the 1st dose. She added that she read that the side effects usually last a couple of days, but hers has not gone away. She queried how will she get rid of the of the headache and if everyone's symptoms eventually go away in the study; and if she will have this headache permanently. The outcome headache was not recovered. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0939436
Sex: F
Age:
State: UT

Vax Date: 12/21/2020
Onset Date: 01/07/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Lower lip edema/Only edema in lower lip; This is a spontaneous report from a contactable nurse reporting for herself. A 45-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) lot number: EK5730, via an unspecified route of administration in the left arm on 21Dec2020 13:00 at a single dose for COVID-19 immunization. Medical history included Graves' disease with hypothyroidism and epilepsy; and had dermal filler 2 months ago (in 2020) in both top and bottom lip. Concomitant medication included levothyroxine. The patient was not pregnant. The patient previously took aspirin bayer and experienced drug hypersensitivity. The patient was not diagnosed with covid prior vaccination nor was she tested post vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced lower lip edema and mentioned that she had dermal filler 2 months ago in both top and bottom lip. Only edema in lower lip. Have image if needed. No changes in medications, no changes in soap, skin care or makeup. The event occurred on 07Jan2021 at 05:00 AM with outcome of not recovered. The event was reported as non-serious. Therapeutic measures were taken as a result of lower lip edema/only edema in lower lip which included famotidine and CLARITIN.

Other Meds:

Current Illness:

ID: 0939437
Sex: F
Age:
State: NC

Vax Date: 01/06/2021
Onset Date: 01/07/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Tingling and mild numbness on dorsal wrist, proximal palm and digits 3-5.; Tingling and mild numbness on dorsal wrist, proximal palm and digits 3-5.; This is a spontaneous report from a contactable nurse (patient). A 40-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) lot number: EK9231, via an unspecified route of administration in the left arm, on 06Jan2021 11:00 at a single dose for COVID-19 immunization. Medical history included chronic migraine and allergies to medications, food, or other products including penicillin. Concomitant medication included ethinylestradiol, levonorgestrel (SRONYX) for birth control. The patient previously took piroxicam and experienced allergy. The patient was not pregnant. The patient was not diagnosed with covid-19 prior to vaccination nor was she tested for Covid-19 since vaccination. She did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced tingling and mild numbness on dorsal wrist, proximal palm and digits 3-5 on 07Jan2021, 10:00 AM, with outcome of not recovered. The events were reported as non-serious with no treatment received.

Other Meds: SRONYX

Current Illness:

ID: 0939438
Sex: M
Age:
State: TX

Vax Date: 12/23/2020
Onset Date: 12/24/2020
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Chills; nausea; dizziness; fatigue; Epi-gastric pain; racing heart; depression; This is a spontaneous report from a contactable healthcare profession (HCP) (patient). A 59-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK5730), intramuscularly on 23Dec2020 11:00 at a single dose in left arm for COVID-19 immunization. Medical history included gastrooesophageal reflux disease (GERD), COVID-prior-vaccination: Yes. No allergies to medications, food, or other products. Concomitant medication included ibuprofen in two weeks. On 24Dec2020, the patient experienced chills, nausea, dizziness, fatigue, epi-gastric pain, racing heart, and depression. AE resulted in Doctor or other healthcare professional office/clinic visit. No treatment received for adverse event. The outcome of events was recovered on 24Dec2020. This is a non-serious report. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient did not test for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine.

Other Meds:

Current Illness:

ID: 0939439
Sex: M
Age:
State: FL

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

Lab Data:

Allergies:

Symptoms: seeing kind of blurry; flu like side effects; sinus aches; This is a spontaneous report from a contactable consumer (patient himself). A 52-year-old male patient the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# EL0140), via an unspecified route of administration on 05Jan2021 in left arm at single dose for prevent getting COVID-19. There were no medical history and concomitant medications. Consumer said he took the COVID-19 vaccine yesterday for where he worked, and had flu like side effects and would like to make sure they are normal. Caller clarified that he got the vaccine on Tuesday, 05Jan2021. He said that the side effects were his body and head hurts. He said that the side effects started yesterday, like the flu, he had body and sinus aches, and was like coughing a little bit with a low fever last night that went away. He said that this morning (06Jan2021) he woke up the same way, then went outside and he was seeing kind of blurry, but not much. He said he came inside and sit down, and was ok again, he felt like he had a big flu in his head. Caller said that he took a picture of the vaccine card, where they kind of wrote on it and it said Pfizer EL0140. Caller said that yesterday and today he woke up the same, so no change to events, he just took over the counter pills for sinus, he didn't want to drink nothing. No further information was provided about the over the counter pills for sinus. Caller said he had no new medications and received no other vaccines when he got the COVID-19 vaccine. Caller said for his fever his wife put her hand on him and said he was kind of hot, but it was nothing big. Temperature was not taken. Outcome of events were unknown.

Other Meds:

Current Illness:

ID: 0939440
Sex: M
Age:
State: WA

Vax Date: 12/30/2020
Onset Date: 12/31/2020
Rec V Date: 01/13/2021
Hospital:

Lab Data: Test Name: blood pressure; Result Unstructured Data: Test Result:165/74; Comments: Raised blood pressure

Allergies:

Symptoms: Raised blood pressure 165/74; aching joints; muscle pain; swelling of the face; fatigue; This is a spontaneous report from a contactable consumer, the patient. A 67-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), lot: el 1284, via an unspecified route of administration in the left arm on 30Dec2020 at 10:45 (at the age of 67-year-old) as a single dose for COVID-19 immunization. Medical history was reported as none. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient had no allergies to medications, food or other products. Concomitant medications included lisinopril and sertaconazole nitrate (SERTALIN); all for unknown indications from unknown dates and unknown if ongoing. The patient did not receive any other vaccines within 4 weeks prior to the vaccination. On 31Dec2020 at 04:00, the patient experienced raised blood pressure of 165/74, aching joints, muscle pain, swelling of the face and fatigue. The events resulted in a doctor or other healthcare professional office/clinic visit, and an emergency room/department or urgent care visit. The patient was not treated for the events. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the raised blood pressure of 165/74, aching joints, muscle pain, swelling of the face and fatigue was resolving.

Other Meds: ; SERTALIN

Current Illness:

ID: 0939441
Sex: F
Age:
State: NY

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data: Test Date: 20210106; Test Name: Fever; Result Unstructured Data: Test Result:101.1

Allergies:

Symptoms: 101.1 Fever; chills; body aches; headache; Eye twitching; Fatigue; This is a spontaneous report from a contactable nurse (patient). An adult non-pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via intramuscular in left arm on 06Jan2021 10:45 at single dose for covid-19 immunization in hospital. Medical history included were none. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. There was no allergies to medications, food, or other products. The patient's concomitant medications were not reported. There was no other vaccine in four weeks. The patient previously took first dose of bnt162b2 on 16Dec2020 05:00 PM via intramuscular in left arm for covid-19 immunization. The patient experienced 101.1 fever, chills, body aches, headache, eye twitching, fatigue on 06Jan2021 16:00. The events were non-serious. The events did not result in emergency room or physician visit. There was no treatment for the events. The outcome of the events was resolving. Information on the Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 0939442
Sex: F
Age:
State: MD

Vax Date: 01/04/2021
Onset Date: 01/06/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: received the second dose in less than 21 days from the first dose; cervical lymphadenopathy; Swelling at location of undereye cosmetic fillers; This is a spontaneous report from a contactable Physician (reporting for herself). A 37-year-old female patient receive BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE Solution for injection), intramuscular on right arm, on 04Jan2021 (lot no: EL1283) 17:00 at a single dose for COVID-19 immunization. Medical history included prolactinoma an patient had infertility. Concomitant medication included ascorbic acid, betacarotene, cupric oxide, manganese sulfate, selenium, tocopheryl acetate, ubidecarenone, zinc oxide (COQ10 [ascorbic acid;betacarotene;cupric oxide;manganese sulfate;selenium;tocopheryl acetate;ubidecarenone;zinc oxide]), ascorbic acid, betacarotene, calcium sulfate, colecalciferol, cyanocobalamin, ferrous fumarate, folic acid, nicotinamide, pyridoxine hydrochloride, retinol acetate, riboflavin, thiamine mononitrate, tocopheryl acetate, zinc oxide (PRENATAL VITAMINS [ascorbic acid;betacarotene;calcium sulfate;colecalciferol;cyanocobalamin;ferrous fumarate;folic acid;nicotinamide;pyridoxine hydrochloride;retinol acetate;riboflavin;thiamine mononitrate;tocopheryl acetate;zinc oxide]), levothyroxine sodium (SYNTHROID), colecalciferol (VITAMIN D [colecalciferol]).; all on unspecified dates (reported as taken within 2 weeks of vaccination) for unspecified indications. The patient had her 1st dose on right arm (lot no: EJ1685, expiry: unknown) of COVID-19 Vaccine on 16Dec2020. She received the second dose in less than 21 days from the first dose. On 06Jan2021, patient experienced swelling at location of undereye cosmetic fillers, right worse than left with mild associated right cervical lymphadenopathy. Patient was given fexofenadine (ALLEGRA) and improvement was seen. Outcome of the events lymphadenopathy cervical and eye swelling recovering. The female was not pregnant. Patient has no COVID prior vaccination. The most recent COVID-19 vaccine was admistered at the hospital and patient has not received any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, patient has not been tested for COVID-19.

Other Meds: COQ10 [ASCORBIC ACID;BETACAROTENE;CUPRIC OXIDE;MANGANESE SULFATE;SELENIUM;TOCOPHERYL ACETATE;UBIDECA; PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS ; SYNTHROID; VITAMIN D [COLECALCIFEROL

Current Illness:

ID: 0939443
Sex: M
Age:
State: GA

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

Lab Data:

Allergies:

Symptoms: episode of tachycardia; This is a spontaneous report from a contactable consumer. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) lot number and expiration date not provided, via an unspecified route of administration from an unspecified date at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient experienced an episode of tachycardia 5 minutes after getting the COVID vaccine. The outcome of the event was unknown. Information on the Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0939444
Sex: F
Age:
State: NY

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

Lab Data:

Allergies:

Symptoms: axillary lymph node swelling/neck lymph node is swollen; This is a spontaneous report from a contactable physician. A female patient of an unspecified age started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) lot number and expiration date not provided, via an unspecified route of administration at the left arm from an unspecified date at a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. It was reported hat the patient had axillary lymph node swelling. It was stated that the patient's neck lymph node is also swollen. This was the patient's first injection and clarified that it was given in her left arm. The outcome of the event was unknown. Information on the lot number/batch number was requested.

Other Meds:

Current Illness:

ID: 0939445
Sex: F
Age:
State: CA

Vax Date: 12/26/2020
Onset Date: 01/02/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data: Test Date: 20201231; Test Name: COVID-19; Result Unstructured Data: Test Result:negative; Comments: actually tested negative 2 days before testing positive; Test Date: 20210102; Test Name: COVID-19; Result Unstructured Data: Test Result:positive

Allergies:

Symptoms: she tested positive for COVID-19 after receiving the first dose of the Pfizer-Biontech COVID-19 vaccine.; she tested positive for COVID-19 after receiving the first dose of the Pfizer-Biontech COVID-19 vaccine.; This is a spontaneous report from a contactable physician. A 41-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EH9899) intramuscular in left arm on 26Dec2020 14:30 at a single dose for COVID-19 immunization.The patient's medical history and concomitant medications were not reported. The physician received her first dose of the COVID vaccine on 26Dec2020 and on 02Jan2021, tested positive for COVID. She actually tested negative 2 days before testing positive (26Dec2020). The outcome of the event was recovered on an unknown date. According to the physician, the event was unrelated to the vaccine as her nanny and her son was also tested positive.; Sender's Comments: The Company cannot completely exclude the possible causality between the reported tested positive for COVID, which is considered ineffective of BNT162B2, and the administration of BNT162B2.

Other Meds:

Current Illness:

ID: 0939446
Sex: F
Age:
State: MS

Vax Date: 01/07/2021
Onset Date: 12/19/2020
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: vaccinated in her arm then was feeling well but had sore arm; This is a spontaneous report from a contactable nurse (reporting for herself). A 19-year-old female patient to received of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), second dose on 07Jan2021 22:45 (lot number: EL1284) and first dose on 17Dec2020 15:30 (lot number: EK5730); via intramuscular in left arm at single dose for COVID-19 immunization. Medical history was reported as none. The patient's concomitant medications were not reported. The patient was vaccinated in her arm then was feeling well but had sore arm on 19Dec2020, comparable to the flu vaccine. The facility where the most recent COVID-19 vaccine was administered was in the workplace clinic. 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. The outcome of the event was recovered on unspecified date. No treatment was given to the patient for the event. The event was considered non serious as it did not results in death, was not life threatening, did not cause/prolonged hospitalization, was not disabling/Incapacitating and had no congenital anomaly/birth defect.

Other Meds:

Current Illness:

ID: 0939447
Sex: M
Age:
State: KS

Vax Date: 12/19/2020
Onset Date: 12/19/2020
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Joint pain in both shoulders and knees; flu like symptoms; This is a spontaneous report from a contactable healthcare professional (patient). A 60-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), second dose on 07Jan2021 and first dose on 19Dec2020 08:00 (lot number: EH9899) in left arm; both via at single dose for COVID-19 immunization. Medical history included high blood pressure from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. On 19Dec2020 10:00, the patient experienced flu like symptoms and joint pain in both shoulders and knees that continued until second shot on 07Jan2021 that eventually subsided. The outcome of the events was recovered with lasting effects on unspecified date. No treatment given to the patient for the events. 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, it was unknown if the patient was diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The events was considered non serious as it did not results in death, was not life threatening, did not cause/prolonged hospitalization, was not disabling/Incapacitating and had no congenital anomaly/birth defect.

Other Meds:

Current Illness:

ID: 0939448
Sex: F
Age:
State: WI

Vax Date: 01/04/2021
Onset Date: 01/05/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: fatigue; headache; body aches; This is a spontaneous report from a contactable healthcare professional reporting for a 42-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL 0142), intramuscular on 04Jan2021 15:30 in left arm at single dose for COVID-19 immunization. Medical history included COVID-19, type 1 diabetes and penicillin allergy from an unknown date and unknown if ongoing. Concomitant medication included insulin. The patient experienced fatigue, headache and body aches on 05Jan2021 10:00. No treatment was given to the patient for the events. 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 diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was recovering. The events was considered non serious as it did not results in death, was not life threatening, did not cause/prolonged hospitalization, was not disabling/Incapacitating and had no congenital anomaly/birth defect.

Other Meds:

Current Illness:

ID: 0939449
Sex: F
Age:
State: VA

Vax Date: 01/06/2021
Onset Date:
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: her arm just feels like she bumped into a door; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received bnt162b2 (BNT162B2 reported as Pfizer-Biontech COVID-19 Vaccine; unknown lot number and expiration date), via an unspecified route of administration on 06Jan2021 at a single dose for covid-19 vaccination. The patient's medical history and concomitant medications were not reported. The patient reported that she was lucky enough to get the vaccine last night and her arm just feels like she bumped into a door. She mentioned that assuming this vaccine is similar to the flu, she inquired are the symptoms less if you contract covid after getting the vaccine. She inquired as well if it is "consider putting in the fact sheet how long after getting before being protected". The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0939450
Sex: F
Age:
State:

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

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

Allergies:

Symptoms: Tested positive for COVID; Tested positive for COVID; This is a spontaneous report received from a contactable Registered Nurse (patient) via a Pfizer sponsored program IBCC (Inbound Call Center for HCPs). A female patient of an unspecified age received BNT162B2, via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced tested positive for COVID on an unspecified date with outcome of unknown. The patient just received the COVID vaccine, and also tested positive for COVID. The patient underwent lab tests and procedures which included COVID test: positive. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0939451
Sex: M
Age:
State: MD

Vax Date: 01/07/2021
Onset Date: 01/07/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: This patient experience left sided numbness (felt like left arm and left leg was heavy); This patient experience left sided numbness (felt like left arm and left leg was heavy); This is a spontaneous report from a contactable pharmacist. A 40-year-old male patient received first dose of bnt162b2 (BNT162B2 reported as COVID-19 vaccine; lot number: EL1284; expiration date: unknown), intramuscular left arm on 07Jan2021 11:00 at a single dose for covid-19 vaccination. The patient has no medical history. The patient has no allergies to medications, food, or other products. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and did not have any other medications the patient received within 2 weeks of vaccination. The patient received the most recent COVID-19 vaccine in a nursing home/senior living facility. This patient experience left sided numbness (felt like left arm and left leg was heavy) on 07Jan2021 11:00 AM. The event was reported as non-serious. The adverse event result in emergency room/department or urgent care visit. No treatment was received for the adverse event. The patient was not diagnosed with COVID-19 prior to vaccination. The patient has not been tested for COVID-19 since the vaccination. The outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 0939452
Sex: F
Age:
State: CA

Vax Date: 01/05/2021
Onset Date: 01/06/2021
Rec V Date: 01/13/2021
Hospital:

Lab Data:

Allergies:

Symptoms: upper right lip swelling; hive on forearm above elbow on left arm; This is a spontaneous report from a contactable nurse (patient). A 39-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EH9899), intramuscular in the left arm on 05Jan2021 15:00 at a single dose for COVID-19 immunization. The patient's medical history included type 2 diabetes. The patient had no known allergies to medications, food, or other products. The patient was not pregnant at the time of vaccination. Concomitant medications included metformin and glucosamine. 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 and had not been tested for COVID-19 since the vaccination. On 06Jan2021 17:00, the patient experienced hive on forearm above elbow on left arm then on 07Jan2021, the patient experienced upper right lip swelling. No treatment was received for the adverse events. Outcome of the events was unknown. The events were considered non-serious by the reporter.

Other Meds: ;

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm