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: 0973321
Sex: F
Age:
State: FL

Vax Date: 12/23/2020
Onset Date: 12/28/2020
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20201228; Test Name: Other covid test; Test Result: Negative ; Test Date: 20201230; Test Name: Other covid test; Test Result: Negative ; Test Date: 20210104; Test Name: Other covid test; Test Result: Negative ; Test Date: 20210108; Test Name: Nasal Swab; Test Result: Negative ; Test Date: 20210111; Test Name: Nasal Swab; Result Unstructured Data: Test Result:unknown result; Comments: pending

Allergies:

Symptoms: I developed jaw pain and intense pain chewing on the right side for 48 hours, plus swelling and pain in the right cheek and right neck lymph nodes.; I developed jaw pain and intense pain chewing on the right side for 48 hours, plus swelling and pain in the right cheek and right neck lymph nodes.; I developed jaw pain and intense pain chewing on the right side for 48 hours, plus swelling and pain in the right cheek and right neck lymph nodes.; I developed jaw pain and intense pain chewing on the right side for 48 hours, plus swelling and pain in the right cheek and right neck lymph nodes.; I developed jaw pain and intense pain chewing on the right side for 48 hours, plus swelling and pain in the right cheek and right neck lymph nodes.; This is a spontaneous report from a contactable other healthcare professional (patient) reported that a 65-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: ELO146), via an unspecified route of administration on right arm on 23Dec2020 12:00 at a single dose for covid-19 immunisation. Medical history included hypertension, osteopenia, hypercholesterolaemia and migraine; all from an unknown date. Patient is not pregnant. The patient had her second dose of pneumonia vaccine on 01Dec2020 that was administered on her right arm for immunization. Concomitant medications included calcium, alendronate sodium (FOSAMAX), losartan, meloxicam and simvastatin; all were taken from an unspecified date for an unspecified indication. The patient previously took naproxen sodium (NAPROSYN) and experienced drug allergy. On 28Dec2020 12:00, the patient developed jaw pain and intense pain chewing on the right side for 48 hours, plus swelling and pain in the right cheek and right neck lymph nodes. The patient did not received any treatment for the reported events. The patient underwent lab tests and procedures which included covid-19: negative on 28Dec2020, on 30Dec2020, on 04Jan2021 and on 08Jan2021 (nasal swab) while on 11Jan2021 (nasal swab) had pending result. The outcome of the events was recovered.

Other Meds: CALCIUM; FOSAMAX; LOSARTAN; MELOXICAM; SIMVASTATIN

Current Illness:

ID: 0973322
Sex: M
Age:
State: SC

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Burn and itching throughout the entire body; Burn and itching throughout the entire body; This is a spontaneous report from a contactable other healthcare professional (HCP) (patient). A 54-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL3302) via an unspecified route of administration in the left arm on 11Jan2021 10:30 AM at a single dose for COVID-19 immunisation. Medical history included diabetes and known allergies to peanuts. Concomitant medications were not reported. The patient previously had known allergies to amoxicillin. The patient experienced burn and itching throughout the entire body on 11Jan2021 which resulted to emergency room/department or urgent care. Treatment for the events included Benadryl. The patient had no COVID prior to vaccination. He did not have COVID tested post vaccination. The patient had no other vaccine in four weeks. The outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 0973323
Sex: F
Age:
State: IL

Vax Date: 12/19/2020
Onset Date:
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: sore arm; This is a spontaneous report from a contactable nurse (patient). This 60-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose on 19Dec2020 for COVID-19 immunization. Medical history included asthma; hypertension; acid reflux; food allergies; known allergies to peanut, shell fish, IVP dye, penicillin and tree nuts. Patient also had known allergies to erythromycin and ceftriaxone (ROCEPHIN). Concomitant medication was not reported. There was no other vaccine in four weeks. On the first dose of 19Dec2020 just a sore arm (date unspecified). The outcome of event was unknown. Information on lot/batch no. has been requested.

Other Meds:

Current Illness:

ID: 0973324
Sex: F
Age:
State: NM

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

Lab Data: Test Name: Vitals; Result Unstructured Data: Test Result:stable; Test Name: O2 saturation; Result Unstructured Data: Test Result:within normal limits

Allergies:

Symptoms: Complaints of sensation of "foreign body" in throat and feeling of throat/tongue swelling; Complaints of sensation of "foreign body" in throat and feeling of throat/tongue swelling; Complaints of sensation of "foreign body" in throat and feeling of throat/tongue swelling; Intermittent episodes of acute sharp back pain; This is a spontaneous report from a contactable pharmacist reported that a 57-year-old female patient (no pregnant) received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine, lot number: EL1284 and Expiration Date unknown) via Intramuscularly on 30Dec2020 03:00 PM (Left arm) at single dose for covid-19 immunisation. Medical history includes mild asthma, B-Cell Thymoma (Resected), multiple allergies. Diagnosed allergies included Sulfa drugs-swelling; Celebrex-Itchy; Clindamycin- Unknown reaction; Doxycycline- Sick to stomach; Iodinated radiocontrast dyes- Iodinated radiocontrast dyes cause generalized swelling (takes diphenhydramine prior to contrast use when needed); Keflex- Rash; TDAP Vaccine; Levofloxacin- Unknown Reaction; Penicillin; Prednisolone- Itchy; Septra- Eyes get glossy and lips swell.The concomitant medication was not reported. There is no other vaccines within 4 weeks prior to the COVID vaccine. About 4 Hours after receiving 1st (of 2) doses of Pfizer COVID-19 Vaccine (30Dec2020 30Dec2020 08:00 PM), Patient went to Emergency room (ER) with complaints of sensation of "foreign body" in throat and feeling of throat/tongue swelling. Also had intermittent episodes of acute sharp back pain while in ER. Upon arrival in ER, patient received routine precautionary care with peripheral IV placement. She was kept under observation in ER for approximately 5 hours until subjective symptoms resolved. On exam patient did not have objective signs of throat obstruction. Vitals were stable and O2 saturation on Room Air was within normal limits. Patient did not receive any medications, oxygen, fluids, or any interventions other than observation. Once symptoms resolved, patient was discharged from ER in improved condition. The outcome of event was recovered on an unknow date without treatment. There is no covid tested post vaccination.

Other Meds:

Current Illness:

ID: 0973325
Sex: F
Age:
State: ND

Vax Date: 01/09/2021
Onset Date: 01/09/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: severe body aches; joint pain; chills; headache; nausea; diarrhea; This is spontaneous report from a contactable nurse (patient). A 47-year-old female patient (non-pregnant) received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot #: EL3249), via an unspecified route of administration on 09Jan2021 11:15 at single dose at right arm for covid-19 immunization. Medical history included mild asthma, known allergies: latex, peanuts from an unknown date and unknown if ongoing, and the patient was diagnosed with COVID-19 prior to vaccination. Patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine, patient didn't receive other medication within 2 weeks of vaccination. The patient's concomitant medications were not reported. Since the vaccination, patient had not been tested for COVID-19. Patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number=EH9899) at single dose at right arm on 19Dec2020 11:15 am for covid-19 immunization. About 12 hours after the vaccination patient had severe body aches, joint pain, chills, headache, nausea, diarrhea on 09Jan2021 09:00 PM. All symptoms lasted from 12-16 hours, except the diarrhea lasted about 20 hours. Outcome of all events was recovered on 10Jan2021. Patient didn't receive treatment for events. The adverse events resulted in neither doctor or other healthcare professional office/clinic visit, nor emergency room/department or urgent care.

Other Meds:

Current Illness:

ID: 0973326
Sex: M
Age:
State: CA

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

Lab Data: Test Date: 20210112; Test Name: temp; Result Unstructured Data: Test Result:99.4 Fahrenheit

Allergies:

Symptoms: After approx 22 hours, a bit chilled, tired; After approx 22 hours, a bit chilled, tired; Went home, dosed a bit, have 99.4 f temp; This is a spontaneous report from a contactable Other-HCP. This 63-year-old male Other-HCP (patient) reported that he received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via intramuscular at left arm on 12Jan2021 02:00 AM at single dose for COVID-19 immunization. Medical history was none. Concomitant medications included diltiazem, tamsulosin. Historical vaccine included the first dose of BNT162B2 via intramuscular at left arm on 21Dec2020 08:00 AM for COVID-19 immunization. No other vaccine in four weeks. No Covid prior vaccination. No Covid tested post vaccination. On 13Jan2021 00:00 AM (after approx 22 hours), patient had a bit chilled, tired; he went home, dosed a bit, had 99.4 f temp. No treatment was received. Outcome of events was not recovered. Information on the lot/batch number has been requested.

Other Meds: DILTIAZEM; TAMSULOSIN

Current Illness:

ID: 0973327
Sex: F
Age:
State: IL

Vax Date: 01/09/2021
Onset Date: 01/10/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20210110; Test Name: fever; Result Unstructured Data: Test Result:100.7; Comments: fever of 100.7 orally

Allergies:

Symptoms: increased postnasal drip; had a fever of 100.7 orally; bodyaches; headache; chills; This is a spontaneous report from a contactable nurse (patient). A 60-year-old female patient (not pregnant) received the second dose of bnt162b2 PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK5730), intramuscular on 09Jan2021 09:30 at single dose in right arm for COVID-19 immunization. Medical history included asthma, hypertension/ Blood pressure, acid reflux, food allergies, Known allergies: tree nuts, peanut, shell fish, Penicillin, Erythromycin, IVP dye, Rocephin. The patient's concomitant medications in two weeks included Blood pressure, acid reflux. The patient previously took the first dose of bnt162b2 on 19Dec2020 for COVID-19 immunization and experienced Sore arm. No other-vaccine-in-four weeks. Second dose on 09Jan2021 within 17 hours had a fever of 100.7 orally, body aches, headache, chills and increased postnasal drip on 10Jan2021 02:30. No treatment received. No covid-prior-vaccination and no covid tested post vaccination. The outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 0973328
Sex: M
Age:
State:

Vax Date: 12/28/2020
Onset Date: 01/09/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: This is a spontaneous report from a non-contactable other health professional (patient). A 37-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL1284), via an unspecified route of administration on 28Dec2020 at single dose for COVID-19 immunization. Medical history was none, the patient was not on any meds. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not have COVID tested post vaccination and did not have COVID prior vaccination. The patient had no known allergies. The patient experienced shingles, painful rash on the flank on 09Jan2021 with outcome of not recovered. The patient took valacyclovir as treatment. The events resulted in doctor or other healthcare professional office/clinic visit. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0973329
Sex: F
Age:
State:

Vax Date: 12/21/2020
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: This is a spontaneous report from a non-contactable nurse (patient). This 22-year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) 1st dose on 21Dec2020 10:00 AM at left arm, and 2nd dose on 11Jan2021 07:45 AM at left arm, both at single dose via an unknown route for COVID-19 immunization. Facility type vaccine was hospital. Medical history was not provided. Patient did not have COVID prior vaccination. Concomitant drug in two weeks included polycarbophil calcium (FIBER). Patient did not have other vaccine in four weeks. No COVID tested post vaccination. Patient's left armpit had an aching pain with movement or palpation. It was also swollen. She thought her lymph nodes were swollen. Event onset date was reported as 12Jan2021 05:00 AM. This also happened with first dose and it lasted for two weeks. No treatment received. Outcome of the events was resolving. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds: FIBER

Current Illness:

ID: 0973330
Sex: F
Age:
State: TX

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

Lab Data:

Allergies:

Symptoms: Rashes to upper body anterior and posterior; Generalized body pain; chest pain; 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, lot# EK5730), intramuscularly in left arm on 01Jan2021 06:15 at single dose for COVID-19 immunization. Medical history was none. Known allergies: No. Other medical history: No. The patient was not pregnant. Concomitant medication in two weeks included colecalciferol (VITAMIN D). If other vaccine in four weeks: No. The patient experienced rashes to upper body anterior and posterior, generalized body pain, chest pain, all on 12Jan2021 17:00 with outcome of not recovered. No treatment received for the events. If covid prior vaccination: No. If covid tested post vaccination: No. AE was not resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care.

Other Meds: VITAMIN D [COLECALCIFEROL]

Current Illness:

ID: 0973331
Sex: F
Age:
State: AL

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

Lab Data: Test Date: 20210104; Test Name: blood pressure; Result Unstructured Data: Test Result: Elevated; Test Date: 20200515; Test Name: COVID; Test Result: Positive; Test Name: Nasal Swab; Test Result: Negative; Comments: post vaccination.

Allergies:

Symptoms: This is a spontaneous report from a contactable other health professional (patient herself). A 32-year-old female patient (non-pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# El1284), via an unspecified route of administration on 30Dec2020 11:45 in right arm at single dose for COVID-19 immunization. Medical history included COVID from 15May2020 to an unknown end date. Known allergies was no. Other medications in two weeks included pantoprazole, cholecalciferol (VIT D3), ascorbic acid (VIT C), zinc, fish oil, curcuma longa (TURMERIC). The patient experienced mild cold like symptoms (runny nose and sore chest) 3 days after vaccine on 02Jan2021, blood spots on right abdomen, chest 3-4 days after vaccine in Jan2021. Constant headache for a week starting 5 days after vaccine on 04Jan2021 and elevated blood pressure, racing heart, and chest pain 5 days after vaccine on 04Jan2021. All events resulted in doctor or other healthcare professional office/clinic visit. The patient underwent lab tests and procedures which included COVID positive on 15May2020. The patient had COVID test of nasal swab post vaccination and result with negative. Outcome of events were unknown. No treatment was received for events.; Sender's Comments: A possible contributory effect of suspect BNT162B2 on reported bleeding cannot be excluded. 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: PANTOPRAZOLE; VIT D3; VIT C; ZINC; FISH OIL; TURMERIC [CURCUMA LONGA]

Current Illness:

ID: 0973332
Sex: F
Age:
State: CA

Vax Date: 12/21/2020
Onset Date: 12/22/2020
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: This is a spontaneous report from a contactable other health professional (patient). A 23-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot/batch number and expiration date not provided), intramuscular on 21Dec2020 16:30 at single dose in left arm, the second dose intramuscular on 12Jan2021 at single dose in left deltoid for COVID-19 immunization. Medical history was none, no known allergies. Concomitant medications included spironolactone, clindamycin, dapsone 5%, vitamin c [ascorbic acid], Multivitamin. Facility type vaccine was Workplace clinic. No other vaccine in four weeks. The patient experienced fatigue, excessive exhaustion, left arm muscle pain, stomach upset/bowel upset on 22Dec2020 20:30. No treatment received. No COVID prior vaccination and no COVID tested post vaccination. The outcome of the events was recovering. Information on the lot/batch number has been requested.

Other Meds: SPIRONOLACTONE; CLINDAMYCIN; DAPSONE; VITAMIN C [ASCORBIC ACID].

Current Illness:

ID: 0973333
Sex: F
Age:
State: PA

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Headache; Myalgia; Fever; Fatigue; The patient experienced chills overnight; This is a spontaneous report from a contactable pharmacist (patient). A 28-year-old no pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number=EK9231), intramuscular in left arm on 06Jan2021 17:45 at single dose for COVID-19 immunization. None Medical history included. Concomitant medication included sertraline and ethinylestradiol, norethisterone acetate (MICROGESTIN). The patient experienced chills overnight (06Jan2021). On 07Jan2021 02:00 am, she experienced fever, headache, myalgia, and fatigue. Self-treated with Acetaminophen. The outcome of events was recovered at unspecified time on 07Jan2021.

Other Meds: SERTRALINE; MICROGESTIN.

Current Illness:

ID: 0973334
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: felt part of the dose run down her arm or at least had that sensation.; This is a spontaneous report from a contactable pharmacist (patient). A 31-year-old female patient received BNT162B2 (Pfizer-BIONTECH Covid-19 Vaccine), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient claimed that on the first dose, she felt part of the dose run down her arm or at least had that sensation. The inoculator thinks the complete dose was injected. The patient was upset and wants a recommendation on if she should need a repeat of her first dose. The patient asked if there was any data on repeating the first dose vs. no action and proceed with the second dose in 21 days. Outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973335
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: bled at the injection site; This is a spontaneous report from a contactable pharmacist. A 4-decade-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for COVID-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. It was reported a female in her 30's bled at the injection site and in unsure if she got the full dose of the vaccine. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973336
Sex: F
Age:
State: OK

Vax Date: 01/08/2021
Onset Date: 01/08/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: I started running a mild fever the next day and I still have a fever today; feel lightheaded; weak; feeling nausea; my legs were weak; my throat got tight; This is a spontaneous report from a contactable HCP. This 44-year-old female (patient) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EK9231) at left arm at single dose for COVID-19 immunization on 08Jan2021 05:30 PM. Relevant medical history included osteoporosis and menopause. Known allergies included: soy, dairy, all nuts, sunflower, cottonwood, lentils, chickpeas, Vit E, cephalexin, Amoxicillin, sulfa, Bactrim, lisinopril , estrogen, moxifloxacin, Pseudoephedrine, paroxetine, trimethoprim, doxycycline, azithromycin, cipro, clindamycin, colestipol. The patient was not pregnant. Relevant concomitant drug included Vit D, calcium, ibuprofen. Five minutes after receiving the vaccine, her throat got tight then she started to feel lightheaded and her legs were weak. She notified the staff there who offered her Benadryl but she declined. She began feeling nausea about an hour later and she felt lightheaded and weak for about 4 hours. She started running a mild fever the next day and she still had a fever on 12Jan2021. The patient did not receive other vaccine in four weeks. The outcome of events was recovering. No treatment was received. The patient was not COVID infected prior vaccination. The patient did not have COVID tested post vaccination.

Other Meds: VIT D; CALCIUM; IBUPROFEN.

Current Illness:

ID: 0973337
Sex: F
Age:
State: CT

Vax Date: 01/09/2021
Onset Date: 01/10/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20210110; Test Name: Heart Rate; Result Unstructured Data: Test Result: 104 BPM.

Allergies:

Symptoms: Labored breathing/shortness of breath; Extreme fatigue; Resting heart rate 104 bpm; Full body myalgias; Nausea; This is a spontaneous report from a contactable pharmacist. A 28-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1686), intramuscular at the left arm on 09Jan2021 17:00 at a single dose for COVID-19 immunization at a clinic. Medical history was reported as none. Patient has no known allergies. The patient was not pregnant. Concomitant medication included desogestrel, ethinylestradiol (VELIVET). The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899), intramuscular at the left arm on 21Dec2020 14:45. The patient experienced full body myalgias, nausea, extreme fatigue, resting heart rate 104 bpm, and labored breathing/shortness of breath on 10Jan2021, 04:30. There was treatment for the adverse events. Patient has not been tested for COVID 19 prior and post vaccination. The patient was recovering from the events.

Other Meds: VELIVET

Current Illness:

ID: 0973338
Sex: M
Age:
State: NJ

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

Lab Data:

Allergies:

Symptoms: Generalized malaise; Chills/rigors; Diaphoresis; This is a spontaneous report from a contactable healthcare professional (patient). A 25-year-old male patient the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EK9231; Expiration date was not reported), intramuscularly on the left arm on 12Jan2021 (17:30) at a single dose for COVID-19 immunization at the hospital. The patient had no relevant medical history. Concomitant medications included minoxidil, biotin, vitamin D3 and vitamin C [ascorbic acid]. The patient had previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EK9899; Expiration date was not reported), intramuscularly on the left arm on 23Dec2020 (when the patient was 25 years old) for COVID-19 immunization. On 13Jan2021 (02:00), the patient had generalized malaise; chills/rigors; and diaphoresis. The patient had received acetaminophen as treatment for the reported events. The outcome of the events, 'generalized malaise', 'chills/rigors' and 'diaphoresis', was recovering. The patient was not diagnosed with COVID-19 prior to the vaccination, and had not been tested since the vaccination.

Other Meds: MINOXIDIL; BIOTIN; VITAMIN D3; VITAMIN C [ASCORBIC ACID].

Current Illness:

ID: 0973339
Sex: F
Age:
State:

Vax Date: 01/08/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
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 Spontaneous report from a Non-contactable Consumer reporting for herself. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 08Jan2021 at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient and her husband received the Covid vaccine last Friday (08Jan2021) and the patient was positive for Covid 19 on Monday (11Jan2021). She was wondering whether she should get the second shot. The outcome of the event was unknown. No follow-up attempts are possible; Information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021034217 same reporter, diff patient

Other Meds:

Current Illness:

ID: 0973340
Sex: F
Age:
State:

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 202101; Test Name: blood sugar; Result Unstructured Data: Test Result:increased

Allergies:

Symptoms: after she has received this shot her blood sugar has increased on Jan2021; it is higher than usual; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received her first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration from 11Jan2021 to 11Jan2021 at a single dose for COVID-19 immunization. Medical history included diabetic. It was reported that the patient got the COVID vaccine and she have diabetes after she has received this shot her blood sugar has increased on Jan2021; it is higher than usual. The outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 0973341
Sex: F
Age:
State: VA

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: Temp; Result Unstructured Data: Test Result: 100.

Allergies:

Symptoms: Severe body aches; Chills; Headache; Temp 100; GI upset; diarrhea; This is a spontaneous report from a contactable physician (patient) reported that a 40-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899), via an unspecified route of administration on the right arm on 11Jan2021 09:30 at a single dose for COVID-19 immunization. The patient medical history was not reported. Concomitant medications included paracetamol (TYLENOL), ibuprofen and biotin, cyanocobalamin, folic acid (MVI 3). The patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EH9899) on 21Dec2020 07:15 on the right arm for COVID-19 immunization. On 11Jan2021 21:30 (reported as 'after 12 hours'), the patient experienced severe body aches, chills, headache and temp 100, then after 48 hours (Jan2021) those symptoms resolved, but had GI upset and diarrhea. The patient underwent lab tests and procedures which included body temperature: 100 (no unit reported) on 11Jan2021. The outcome the events severe body aches, chills, headache and temp 100 was recovered on Jan2021 (reported as after 48 hours those symptoms resolved) while GI upset and diarrhea was recovering. The patient did not received any treatment for the reported events.

Other Meds: TYLENOL; IBUPROFEN; MVI 3.

Current Illness:

ID: 0973342
Sex: M
Age:
State:

Vax Date: 01/09/2021
Onset Date: 01/10/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: "pretty big" right arm swelling; flu-like symptoms the day after vaccination; vesicle formation on his one big toe; Herpes Whitlow; This is a spontaneous report from a contactable HCP reported for self. This 65-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number unknown) via unspecified route of administration on 09Jan2021 at single dose for COVID-19 immunization. The patient medical history and concomitant mediations was not provided. The patient experienced reported "pretty big" right arm swelling, and flu-like symptoms the day after vaccination (10Jan2021), both of which have resolved. He is asking about the incidence of what he described as "Herpes Whitlow" vesicle formation on his one big toe. The patient stated that it could be from beginning to run after a couple week hiatus. The patient stated he had been running which he hadn't been doing for a week or two. He has reviewed the literature and can find nothing. The outcome of events swelling in the right arm, and flu-like symptoms was resolved. The outcome of other events was unknown. Information on the Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973343
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Fever blister on her lip; This is a spontaneous report from a contactable pharmacist from a Pfizer sponsored program. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration on 12Jan2021 at a SINGLE DOSE for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that she got the vaccine yesterday and woke up this morning with a fever blister on her lip on 13Jan2021 . She was asking if it was okay for her to take Valtrex and if it would affect the efficacy of the vaccine. The patient was also asking if patients can take Tylenol prior to the shot as preemptive measures for side effects like fever. She also mentioned that she heard from somewhere that there were reports regarding infertility with the vaccine. She was confirming if this was true. She stated, "I get that there's still limited information, with this being all new in all, but it is kind of worrisome on our part as well because we just don't want to mess up administration of this vaccine." She mentioned that she heard from somewhere that there were reports regarding MS (Multiple Sclerosis) side effects with the vaccine. She was also confirming if this was true. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973344
Sex: F
Age:
State: WI

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: fever; Result Unstructured Data: Test Result:low grade; Comments: low grade fever

Allergies:

Symptoms: low grade fever; rigors; myalgias; headache; skin hurt; unable to stand without feeling like passing out; This is a spontaneous report from a contactable other hcp. A 46-year-old female patient received the 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration on the right arm on 11Jan2021 17:15 at a SINGLE DOSE for covid-19 immunisation. Medical history included lichen sclerosus from an unknown date and unknown if ongoing. Concomitant medication included ibuprofen (IBUPROFEN), caffeine, paracetamol (EXCEDRIN [CAFFEINE;PARACETAMOL]). The patient previously had the first dose of BNT162B2 on 21Dec2020. The patient experienced low grade fever, rigors, myalgias, headache, skin hurt, unable to stand without feeling like passing out on 11Jan2021 18:00. The patient underwent lab tests and procedures which included body temperature: low grade on 11Jan2021. No treatment were received for the events. The outcome of events was recovering. Information of lot/batch number has been requested.

Other Meds: IBUPROFEN; EXCEDRIN [CAFFEINE;PARACETAMOL]

Current Illness:

ID: 0973345
Sex: F
Age:
State: NJ

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

Lab Data:

Allergies:

Symptoms: Very tired; This is a spontaneous report from a contactable other hcp. A 60-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration on the left arm on 12Jan2021 14:30 at a SINGLE DOSE for covid-19 immunisation. Medical history included rheumatoid arthritis from an unknown date and unknown if ongoing. Concomitant medication included ascorbic acid, ergocalciferol, nicotinamide, retinol, riboflavin, thiamine hydrochloride (VITAMINS [ASCORBIC ACID;ERGOCALCIFEROL;NICOTINAMIDE;RETINOL;RIBOFLAVIN;THIAMINE HYDROCHLORIDE]). The patient experienced very tired on 12Jan2021 with outcome of recovering. Information on the lot/batch number has been requested.

Other Meds: VITAMINS [ASCORBIC ACID;ERGOCALCIFEROL;NICOTINAMIDE;RETINOL;RIBOFLAVIN;THIAMINE HYDROCHLORIDE]

Current Illness:

ID: 0973346
Sex: F
Age:
State: TN

Vax Date: 12/31/2020
Onset Date: 01/03/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Name: Covid-19 virus test; Result Unstructured Data: Test Result:positive; Comments: Caller is COVID positive after taking the first dose

Allergies:

Symptoms: Caller is COVID positive after taking the first dose; Caller is COVID positive after taking the first dose; got sick; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EJ1686), via an unspecified route of administration on 31Dec2020 at a single dose for COVID-19 immunization. The patient's medical history was not reported. Concomitant medications included levothyroxine sodium (SYNTHROID), duloxetine hydrochloride (CYMBALTA), vitamin C, vitamin E, propanolol hcl and clonazepam (KLONOPIN). Reporter is a social worker at a community center for pediatrics. She had the first dose of the COVID-19 vaccine on 31Dec2020. However, she got sick past Sunday (03Jan2021) and tested positive for COVID-19. She was wondering if there is a chance that the vaccine caused the positive result for the COVID test. Consumer stated, "I had a question about the COVID vaccine and I had the COVID vaccine administered on let's say it was 31Dec and I felt sick over the weekend and ended up having to take a COVID test. Well, the COVID test came out positive for COVID. And so my question is because I had the vaccine could the vaccine maybe cause a false positive test?" The patient underwent lab tests and procedures which included SARS-COV-2 test: positive on an unspecified date (Caller is COVID positive after taking the first dose). The outcome of the events was unknown.

Other Meds: SYNTHROID; CYMBALTA; Vitamin C; Vitamin E; Propanolol HCl; KLONOPIN

Current Illness:

ID: 0973347
Sex: F
Age:
State: IL

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

Lab Data:

Allergies:

Symptoms: Fever; Chills; Headache; Body aches; Extreme fatigue; This is a spontaneous report from a contactable other healthcare professional. A 62-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EL1283; expiry date: unknown) via an unspecified route of administration, on 12Jan2021 at 10:00 in the left arm, at a single dose, for COVID-19 immunization. Relevant medical history included rheumatoid arthritis, allergic rhinitis, sulfonamide allergy, and allergy to capsicum. Concomitant medications included adalimumab (HUMIRA), hydroxychloroquine, leflunomide and other unspecified medications. The patient previously received first dose of (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: FL0140; expiry date: unknown) on 22Dec2020 at 15:00 in the left arm, for COVID-19 immunization. The patient is not pregnant at the time of vaccination. The patient was not diagnosed with COVID prior vaccination. The patient did not receive other vaccines within four weeks prior to COVID vaccination. The vaccine was administered in the hospital. On 12Jan2021, at 23:00 (on the same day after the injection), the patient experienced fever, chills, headache, body aches, and extreme fatigue. The patient did not receive treatment for the events. The patient was recovering from the events. The patient has not been tested for COVID-19 since vaccination.

Other Meds: HUMIRA; HYDROXYCHLOROQUINE; LEFLUNOMIDE

Current Illness:

ID: 0973348
Sex: F
Age:
State: GA

Vax Date: 01/08/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: nerve pain began in feet, arms and hands; This is a spontaneous report from a contactable healthcare professional (patient). A 59-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3246, expiry date not reported), via an unspecified route of administration in the right arm on 08Jan2021 11:30 at single dose for COVID-19 immunization. Medical history included ongoing ideopathic neuropathy and high cholesterol. Concomitant medications included duloxetine (DULOXETINE), acetylsalicylic acid (ASPIRIN BP), and simvastatin (ZOCOR). The patient experienced nerve pain which began in feet, arms and hands on 12Jan2021. No treatment was received for the adverse events. Clinical outcome of the event was not recovered.

Other Meds: DULOXETINE; ASPIRIN BP; ZOCOR.

Current Illness: Neuropathy.

ID: 0973349
Sex: F
Age:
State:

Vax Date: 12/31/2020
Onset Date: 12/31/2020
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20201231; Test Name: heart rate; Result Unstructured Data: Test Result:120s to 140s, 150s

Allergies:

Symptoms: heart rate went up to the 120s or 150s; chills; fever; This is a spontaneous report from a contactable healthcare professional (HCP [patient]). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, batch/lot number and exp date not reported), via an unspecified route of administration on 31Dec2020 for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient had the first dose of the COVID-19 vaccine last 31Dec2020 and did not have any immediate adverse effect. During the night of 31Dec2020, she experienced chills and fever, but the patient wasn't concerned because she knows other people experience it too: some individuals she knew were getting, the fever (could not be clarified further). She was concerned since she had fast heartbeat. Her heart rate went up to the 120s or 150s (ranging to 120s to 140s, 150s). She was concerned if she should go to the hospital to get an IV bolus. Patient had to go to the ER and they gave her some IV Bolus. Patient asked if she should be concerned about the second dose. The outcome of the events was unknown. Information on the batch number/lot number has been requested.; Sender's Comments: Based on a compatible temporal association, a causal relationship between event "heart rate went up to the 120s or 150s" and BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) cannot be completely excluded. 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: 0973350
Sex: F
Age:
State:

Vax Date: 12/21/2020
Onset Date: 12/21/2020
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20201231; Test Name: COVID; Result Unstructured Data: Test Result:diagnosed with COVID; Comments: 10 days later after first dose

Allergies:

Symptoms: received COVID vaccine first dose on 21Dec2020. 10 days later I was diagnosed with COVID; received COVID vaccine first dose on 21Dec2020. 10 days later I was diagnosed with COVID; dizziness; nausea; vomiting; diarrhea; This is a spontaneous report from a contactable pharmacist (reported for herself). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number and expiry date: not known), via an unspecified route of administration on 21Dec2020 at single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received COVID vaccine first dose on 21Dec2020. 10 days later (31Dec2020), the patient was diagnosed with COVID. Her work cancelled her second COVID vaccine until she was symptom free. The patient asked when she should receive her 2nd COVID vaccine. The patient also had a reaction to the first COVID vaccine (dizziness, nausea, vomiting, diarrhea) about 1.5 hours after getting the vaccine at her work on 21Dec2020. She was worried about having strong reaction to 2nd dose since she actually had COVID. The outcome of the events was unknown. Information on the batch/lot number has been requested.; Sender's Comments: The subject received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 21Dec2020, and 10 days later she was diagnosed with COVID. No effect of the suspect vaccine could be reasonably achieved to protect from the targeted infection/disease due to the very short time lag. Instead, the reported COVID likely represents a pre-existing infection prior to vaccine use. Further information is needed for full medical assessment.

Other Meds:

Current Illness:

ID: 0973351
Sex: M
Age:
State: NC

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

Lab Data:

Allergies:

Symptoms: pain on swallowing in the throat; throat started feeling itchy; pins and needles feeling; throat was swollen; This is a spontaneous report from a contactable other healthcare professional (patient). A 35-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) Solution for injection (lot number: EL0140, expiry date unknown), via an unspecified route of administration on the left arm on 12Jan2021, 9:00AM at a single dose for COVID-19 immunization. The patient's medical history included asthma and allergies to Amoxicillin, Quinolones, and Sulfa drugs, all from an unknown date and unknown if ongoing. Concomitant medications included colecalciferol (VITAMIN D) and cyanocobalamin (VITAMIN B 12); patient received these medications with two weeks of vaccination. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient had not been tested for COVID-19. On 12Jan2021, 19:00, just after evening, patient's throat started feeling itchy and had pins and needles feeling. Gradually the symptoms increased in intensity and in the night of 12Jan2021 (time unspecified), he felt like his throat was swollen. It was also reported that patient woke up today, 13Jan2021 with the same feeling and there is pain on swallowing in the throat. No therapeutic measures were taken in response to the events. Outcome of the events was reported as recovering.; Sender's Comments: Based on a chronological association, causality between events odynophagia, pharyngeal swelling and throat irritation and BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) cannot be completely excluded. 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: VITAMIN D [COLECALCIFEROL]; VITAMIN B 12 [CYANOCOBALAMIN]

Current Illness:

ID: 0973352
Sex: F
Age:
State: IL

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Nausea; Headache; Body aches more in the legs; Body aches more in the legs; Low grade fever; Chills; Mild dizziness; Intermittent heart racing; This is a spontaneous report from a contactable nurse (patient). A 50-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3248), via an unspecified route of administration (right arm) on 11Jan2021 (20:00) at single dose for Covid-19 immunization. The patient received the first dose of COVID 19 vaccine (BNT162B2, lot number: EJ1685), via an unspecified route of administration (left arm) on 21Dec2020 (03:30 PM) at single dose for Covid-19 immunization. The patient's medical history included idiopathic neuropathy to bilateral feet; no known allergies. Concomitant medication included tramadol. 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 experienced nausea, headache, body aches more in the legs, low grade fever, chills, mild dizziness, and intermittent heart racing on 12Jan2021 (08:00 AM). There was no treatment received for the adverse events. The outcome of events was recovering. The patient has not been tested for COVID-19 since the vaccination.

Other Meds: TRAMADOL

Current Illness:

ID: 0973353
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: Injection site soreness; This is a spontaneous report from a non-contactable nurse. An adult female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL3302; Expiration date was not reported), intramuscularly on the left arm on 12Jan2021 (14:45) at a single dose for COVID-19 immunization at the hospital. Medical history included adult onset asthma; gastroesophageal reflux disease (GERD); and breast cancer. The patient's concomitant medications were not reported. The patient had previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL0142; Expiration date was not reported), intramuscularly on the left arm on 22Dec2020 for COVID-19 immunization. On 13Jan2021 (06:00), the patient had injection site soreness. The patient did not receive any treatment for the reported event. The outcome of the event, injection site soreness, was not recovered. The patient was not diagnosed with COVID-19 prior to the vaccination, and had not been tested post-vaccination. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0973354
Sex: F
Age:
State: NY

Vax Date: 01/07/2021
Onset Date: 01/07/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Sore arm at the injection site; This is a spontaneous report from a contactable consumer (patient). A 51-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number and expiration date were not reported) on 07Jan2021 at a single dose on the arm, with route of administration unspecified, for COVID-19 immunization. Medical history included acid reflux. The patient's concomitant medication included an unspecified acid reflux medication. On 07Jan2021, the patient had sore arm at the injection site. The outcome of the event, sore arm at the injection site, was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 0973355
Sex: F
Age:
State: TX

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Fatigue; Sensitive skin; Chills; Body aches; This is a spontaneous report from a non-contactable other healthcare professional (patient). A 29-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EK4176), intramuscular in the left arm on 11Jan2021 12:30 at a single dose for COVID-19 immunization. The patient's medical history included diagnosed with COVID-19 prior to vaccination. Concomitant medications were not reported. The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: ek5730), intramuscular in the left arm on 12Dec2020 11:30 at the age of 28 years old for COVID-19 immunization. The patient had not been tested for COVID-19 since the vaccination. On 11Jan2021 20:00, the patient experienced fatigue, body aches, sensitive skin, and chills. No treatment was received for the adverse events. Outcome of the events was recovered on Jan2021. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 0973356
Sex: F
Age:
State:

Vax Date: 01/04/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
Hospital:

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

Allergies:

Symptoms: Tested positive; Tested positive; This is a spontaneous report from a contactable pharmacist. A (23 unknown unit) female patient received first dose of bnt162b2 (Pfizer-BioNTech COVID-19 mRNA vaccine, Lot/Batch Number and Expiration Date unknown) via an unspecified route of administration on 04Jan2021, at single dose for COVID-19 immunization. The patient's medical history and concomitant medications was not reported. Patient received the covid 19 vaccine on 04Jan2021 and tested positive on 11Jan2021, when should patient receive the second dose. The outcome of event was unknown. Information about Lot/Batch has been requested.; Sender's Comments: The patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE) on 04Jan2021, and COVID-19 test positive on 11Jan2021. No effect of the suspect vaccine could be reasonably achieved to protect from the targeted infection/disease due to the very short time lag. Instead, the positive COVID test possibly represents a pre-existing infection prior to vaccine use. Further information is needed for full medical assessment.

Other Meds:

Current Illness:

ID: 0973357
Sex: F
Age:
State: KY

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

Lab Data: Test Date: 2020; Test Name: antibody test; Test Result: Negative ; Comments: She has had an antibody test, in which they draw blood, it was negative but that was even before she caught covid, it was back in Aug2020 or Sep2020.; Test Date: 202011; Test Name: Nasal swab; Test Result: Positive

Allergies:

Symptoms: headache; tiredness/overwhelming feeling of tiredness; nausea; feeling "funny" in the head; a funny taste in the mouth; This is a spontaneous report from a contactable consumer. A 48-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), via an unspecified route of administration on 13Jan2021 07:50 at a single dose on Left Upper Arm Muscle for COVID-19 immunization. Medical history included thyroid disorder and antidepressant therapy. Concomitant medication included levothyroxine sodium (SYNTHROID) for thyroid disorder, duloxetine hydrochloride (CYMBALTA) as Antidepressant and multivitamins. The patient stated that she is calling about the COVID Vaccine, she just had the shot at 7:50AM this morning. After getting the shot she heard that she is not suppose to get the shot if she had tested positive for COVID before the vaccine. She wanted to know if this was true or a rumor. Back around Nov2020 she did test positive for COVID. It was the week before the holidays on Wednesday 18Nov2020 when she lost taste and smell, she then got tested on 19Nov2020 Thursday then got results Friday or Saturday morning, the weekend before the holidays that she was positive. The test was a nasal swab. The girls in the office said she was not suppose to get the shot if it had not been 3 months. When she had COVID shot they didn't tell her if she could take it or not. This morning she woke up everything was fine, she drove over to get vaccine, after they put the vaccine in, they made her wait 15- 30 minute, while waiting she was getting a headache, then the headache went away and she then felt funny in the head. She was a little nauseous then that went away. Then she had this overwhelming feeling of tiredness like she could go to bed. She felt bad a little bit. When she then drove back to work at the school she had this funny taste in the mouth. Her boss wanted to call and see if this is all normal. The date of first dose was 13Jan2021, all the symptoms she experienced occurred within half hour of receiving the vaccine. She thinks she is fine. At the moment she does not have the taste in mouth any longer and her headache left. She still feels funny in head as well as she just feels bad inside, she has the feeling of overwhelming tiredness, she just feels like something is coming on, like she knows she is getting sick. She has no Lot or Expiry to share, she vaccine CDC card is outside in the car and not physically with her. Her drive to get the vaccine was an hour away to a Hospital and all the medication was taken an hour before. She went to the hospital to have the vaccine administered. Then she drove to work at a school. She has had an antibody test, in which they draw blood, it was negative but that was even before she caught COVID, it was back in Aug2020 or Sep2020. She has had no issues with vaccines in the past. The outcome of the event headache, a funny taste in the mouth, and nausea was recovered on 13Jan2021, tiredness/overwhelming feeling of tiredness was unknown, feeling "funny" in the head was not recovered. The events were assessed as non-serious. Information about lot/batch number has been requested.

Other Meds: SYNTHROID; CYMBALTA

Current Illness:

ID: 0973358
Sex: F
Age:
State: TX

Vax Date: 12/22/2020
Onset Date:
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Sleeplessness. I could not sleep after my first and second dose; This is a spontaneous report from a contactable physician (patient). A 32-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date not reported), via an unspecified route of administration on 22Dec2020 14:45 at a single dose on left arm, and the second dose via an unspecified route of administration on 12Jan2021 11:30 (lot number and expiry date not reported) at a single dose on left arm for COVID-19 immunization. Medical history included migraine and allergic to avocados. Concomitant medication included biotin (BIOTIN), keratin (KERATIN). The patient experienced sleeplessness and stated, "I could not sleep after my first and second dose." No treatment received for the event. The outcome of the event was recovered with sequelae. The patient was not pregnant. Facility type vaccine was Workplace clinic. No other vaccine in four weeks. Not diagnosed with COVID prior vaccination. Not tested for COVID post vaccination. Information on the Batch/Lot number has been requested.

Other Meds: BIOTIN; KERATIN

Current Illness:

ID: 0973359
Sex: F
Age:
State: NY

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Woke up in excruciating pain; Fever; Joint and muscle pain; Joint and muscle pain; This is a spontaneous report from a contactable consumer (patient). A 42-year-old female patient received the second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: ej1685), via an unspecified route of administration on 11Jan2021 16:00 at a single dose on left arm for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: ej1685), via an unspecified route of administration on 21Dec2020 04:00 PM at a single dose on left arm for COVID-19 immunization. On Tuesday morning, 12Jan2021, patient woke up in excruciating pain. She had fever, joint and muscle pain. The outcome of the events was recovering. Facility type vaccine was Workplace Clinic. No other vaccine in four weeks. Not diagnosed with COVID prior vaccination. Not tested for COVID post vaccination.

Other Meds:

Current Illness:

ID: 0973360
Sex: F
Age:
State: WA

Vax Date: 01/10/2021
Onset Date: 01/10/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Vomiting; Diarrhea; Patient has become aggressive, combative; Short tempered; Up and down most of the night; delusional; confused; This is a spontaneous report from a contactable consumer. A 88-year-old female patient received the first does of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 10Jan2021 13:30 at a SINGLE DOSE for COVID-19 immunization. Medical history included dementia from an unknown date and unknown if ongoing and COVID-19 prior vaccination. Concomitant medication included gabapentin (GABAPENTIN), hydrocodone (HYDROCODONE), haloperidol (HALDOL), levothyroxine (LEVOTHYROXINE), insulin aspart (NOVOLOG) , lisinopril (LISINOPRIL), lorazepam (LORAZEPAM), sennoside a+b (SENNA [SENNOSIDE A+B]), trazodone (TRAZODONE). The night after the vaccine was administered (10Jan2021), the patient experienced a bad case of vomiting and diarrhea. The patient has become aggressive, combative and short tempered. She was up and down most of the night, delusional and confused. Therapeutic measures (Lorazepam) were taken as a result of the events. The outcome of the events was not recovered. Information on the lot/batch number has been requested.

Other Meds: GABAPENTIN; HYDROCODONE; HALDOL; LEVOTHYROXINE; NOVOLOG; LISINOPRIL; LORAZEPAM; SENNA [SENNOSIDE A+B]; TRAZODONE.

Current Illness:

ID: 0973361
Sex: M
Age:
State: CA

Vax Date: 01/06/2021
Onset Date: 01/06/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20210106; Test Name: Fever; Result Unstructured Data: Test Result:102.0; Test Date: 202101; Test Name: Fever; Result Unstructured Data: Test Result:Low grade

Allergies:

Symptoms: Loss of appetite; Axillary lymph nodes swollen and tender; Axillary lymph nodes swollen and tender; Chills; Headache; Body aches; Nausea; Fatigue; Fever at 102.0; This is a spontaneous report from a contactable nurse (patient). A 38-year-old male patient received the second dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: ECL284), via an unspecified route of administration in left arm, on 06Jan2021 at 08:00, at a single dose, for COVID-19 immunization. The patient's medical history included allergies to penicillin (PCN). The patient's concomitant medications included valaciclovir, zinc, ergocalciferol (VIT D), and an unspecified multivitamin. The patient previously took the first dose of BNT162B2 (Lot Number: EH9899) on 16Dec2020 (10 AM in left arm) for COVID-19 immunization. The patient was not diagnosed with COVID-19 prior to vaccination. The patient was not administered with other vaccine in four weeks. The COVID-19 vaccine was administered in a hospital. On 06Jan2021 at 08:30 PM (around 12 hours later), the patient experienced chills, headache, body aches, nausea, fatigue, and fever at 102.0. Symptoms went on for three days. Fever after initial fever was low grade fever. At day 3 (09Jan2021), left axillary lymph nodes swollen and tender. Some lingering fatigue and loss of appetite 6 days post vaccine (12Jan2021). No treatment was received for the adverse events. Post-vaccination, the patient has not been tested for COVID-19. At the time of reporting, the patient recovered from the events in Jan2021.

Other Meds: VALACYCLOVIR [VALACICLOVIR]; ZINC; VIT D

Current Illness:

ID: 0973362
Sex: F
Age:
State: TX

Vax Date: 01/11/2021
Onset Date: 01/11/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20210111; Test Name: heartbeat; Result Unstructured Data: Test Result:Rapid; Comments: at 12:00 PM,

Allergies:

Symptoms: Face numbness; Headache; Fatigue; Legs aching; Muscle soreness in the left arm; Rapid heartbeat; This is a spontaneous report from a contactable health care 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 11Jan2021 at single dose for COVID-19 immunisation. Vaccine location was left arm. Medical history included frequent migraines, anxiety and anemia. Historical vaccine included first dose of BNT162B2 (Lot # 1), intramuscular left arm, on 21Dec2020 at 07:30 AM for COVID-19 immunisation. Age at vaccination was 40-years-old for both doses. Concomitant medications included topiramate (TOPAMAX), ascorbic acid, cyanocobalamin, ergocalciferol, nicotinamide, pyridoxine hydrochloride, retinol, riboflavin, thiamine mononitrate (ONE DAY VITAMINS), phentermine, phendimetrazine tartrate (BONTRIL), naproxen sodium (ALEVE), escitalopram. On 11Jan2021 at 12:00 PM, the patient experienced face numbness, headache, fatigue, legs aching, muscle soreness in the left arm, and rapid heartbeat. No treatment was received for the event. Outcome was recovering. Information on the lot/batch number has been requested.

Other Meds: ALEVE; BONTRIL; ESCITALOPRAM; PHENTERMINE; TOPAMAX; ONE-A-DAY [ASCORBIC ACID;CYANOCOBALAMIN;ERGOCALCIFEROL;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RETINOL

Current Illness:

ID: 0973363
Sex: M
Age:
State: PA

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

Lab Data: Test Date: 20210112; Test Name: temperature; Result Unstructured Data: Test Result:fever

Allergies:

Symptoms: Fever; Body aches; Chills; Tremors; Headache; This is a spontaneous report received from a contactable other healthcare professional (who is also the patient). A 32-year-old male patient received the second dose of BNT162B2 (BNT162B2 PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3246, expiry date: unknown), intramuscular in the left arm, on 12Jan2021 07:30, at single dose, for COVID-19 immunization, in the hospital. Medical history included Sleep apnea, asthma, gastrooesophageal reflux disease (GERD), hypertension and anxiety. The patient did not have COVID-19 prior to vaccination. The patient had no known allergies. Historical vaccines included diphtheria vaccine toxoid, pertussis vaccine acellular, tetanus vaccine toxoid (TDAP), via an unspecified route of administration in the left arm, on 29Dec2020 for immunization; and the first dose of BNT162B2 (BNT162B2 PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL0140, expiry date: unknown), intramuscular in the left arm, on 21Dec2020 15:15, for COVID-19 immunization. The patient experienced fever, body aches, chills, tremors and headache on 12Jan2021 23:00. The patient did not receive treatment for the events. The patient was not tested for COVID-19 post vaccination. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 0973364
Sex: F
Age:
State: AZ

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: Achy legs/Sore arm; Weak and very tired; Weak and very tired; Slight headache; This is a spontaneous report from a contactable nurse (patient). A 59-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1283, expiry date not reported), via an unspecified route of administration in the left arm on 11Jan2021 14:45 at single dose for COVID-19 immunisation. Medical history included multiple sclerosis and Raynaud's phenomenon. Concomitant medication included natalizumab (TYSABRI) from 30Dec2020. The patient previously took and experienced allergies with celecoxib (CELEXIA), amoxicillin, desipramine and pantoprazole. 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. Since the vaccination, the patient has not been tested for COVID-19. The patient previously took first dose of bnt162b2 (lot number: EH9899, expiry date not reported), via an unspecified route of administration in the left arm on 21Dec2020 13:30 at single dose for COVID-19 immunisation. On 12Jan2021, the patient had achy legs. The patient was also weak and very tired that afternoon, with slight headache. She was much better on 13Jan2021. Her sore arm developed the day after vaccination after both injections lasted a day or two. No treatment was received for the adverse events. Clinical outcome of the events was recovered on Jan2021.

Other Meds: TYSABRI

Current Illness:

ID: 0973365
Sex: F
Age:
State:

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

Lab Data:

Allergies:

Symptoms: fatigue/feeling tired; chills; is not feeling great; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age started to receive bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration from Jan2021 to Jan2021 at a single dose for COVID-19 vaccination. The patient's medical history and concomitant medications were not reported. It was reported that the patient has fatigue/feeling tired and chills and is not feeling great; all on unspecified dates. The outcome of the events was unknown. Information on the Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 0973366
Sex: M
Age:
State: LA

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

Lab Data: Test Date: 20210113; Test Name: fever; Result Unstructured Data: Test Result:100.5

Allergies:

Symptoms: headache; nausea; chills; fever 100.5; fatigue; just not felling well; just want to continue to sleep; This is a spontaneous report from a contactable consumer (patient). This 72-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE Lot # EK5730), via an unspecified route of administration, on 12Jan2021 at 01:00 PM in the right arm at single dose for COVID-19 immunisation. Facility type vaccine was workplace clinic. Age at vaccination was 72-years-old. Medical history included diabetes type 2, hip replacement, prior heart attack, diverticulitis, heart stints. The patients had taken other unspecified medications in two weeks. On 13Jan2021 at 06:00AM, morning after vaccine, the patient woke up with headache, nausea, chills, fever at 100.5, fatigue and just not felling well, just want to continue to sleep. No treatment was received for the events. Outcome was not recovered.

Other Meds:

Current Illness:

ID: 0973367
Sex: F
Age:
State: FL

Vax Date: 01/10/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Date: 20210113; Test Name: blood pressure; Result Unstructured Data: Test Result:188/90; Test Name: labs; Result Unstructured Data: Test Result:Unknown Results; Comments: a week prior. This was not related to her headache

Allergies:

Symptoms: her blood pressure is 188/90; bad headache; This is a spontaneous report from a contactable consumer. An 83-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL1283), via an unspecified route of administration in right arm on 10Jan2021 at a single dose for protection from the virus. Medical history included a month ago on Dec2020, she fell on her right knee and has gotten a shot in her knee for pain. She was going to chiropractor and then started going to an orthopedic doctor. That is when she got a shot in her knee. She had an appointment with her doctor on 29Dec2020. She had labs a week prior. The patient's concomitant medications were not reported. The patient received Covid-19 vaccine on Sunday, 10Jan2021. Yesterday, 12Jan2021, she started having a bad headache. She took Tylenol and it went away. This am of 13Jan2021 at 7:00am, she started having a terrible headache. She also checked her blood pressure and it was 188/90. She took Tylenol around 7:15-7:30. She still has a headache. The outcome of the event headache was not recovered. the outcome of the event blood pressure and it was 188/90 was unkown.

Other Meds:

Current Illness:

ID: 0973368
Sex: F
Age:
State: MI

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: her brain is going blank; back pain that occurs in her left leg past the knee until the top of her foot; back pain that occurs in her left leg past the knee until the top of her foot; She wanted to know if it is like a sciatic nerve pain she is experiencing; she just thought it was swelling in her spine; This is a spontaneous report from a contactable consumer (patient). A 72-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) lot no: EK9231, via an unspecified route of administration in left shoulder on 11Jan2021 at a single dose for covid-19 immunization. Medical history included other problems before taking the COVID-19 vaccine such as joint pain, muscle pain, back pain, spinal stenosis, has a lot of back issues, like sciatic has a lot of problems. There were no concomitant medications. The patient had the COVID-19 vaccine on Monday (11Jan2021). On Tuesday (12Jan2021), she experienced back pain that occurs in her left leg past the knee until the top of her foot. She also mentioned that she had other problems before taking the COVID-19 vaccine such as joint pain, muscle pain, back pain, and spinal stenosis. She wanted to know if the COVID-19 vaccine can cause the adverse event that she experienced. She wanted to know if it is like a sciatic nerve pain she is experiencing. The patient stated it may sound crazy, but she got the COVID 19 vaccine on Monday, she is 72 years old, and has a lot of back issues, like sciatic has a lot of problems, and she got the shot and Tuesday) morning, her back hurt so bad, down into her sciatic, into her butt, leg, her lower leg and as far as her foot, the top of her foot, and she doesn't know if this is something that was going to happen, she read about joint pain, tiredness, that would include joints in the back, she would expect. She wonders if she is out of her head, since it was the very next morning, this was Tuesday, and instantly, she was sitting with ice and trying to get ahold of her healthcare person, she gets pain shots in her back, but she hasn't had them in a couple years, she was going along pretty good, then this was bad enough, it is in her thigh and leg, and is always under her foot, and she just thought it was swelling in her spine. She wonders if it is a side effect or her imagination. When asked for address, the patient stated her brain is going blank. She stated this may be just her. She has bad back problems, and was going along pretty good, it has been a year or two since she has had any kind of anything. But this was a good one, a strong one, the ice hurts so bad. She woke up with it, it is staying the same- after having something like this, she was trying to get ahold of the pain clinic, to get a shot, but that may be 3-4 weeks out. She has had no blood work in a while. Outcome of the events "she just thought it was swelling in her spine" and "her brain is going blank" was unknown; while not recovered for other events.

Other Meds:

Current Illness:

ID: 0973369
Sex: F
Age:
State: PA

Vax Date: 01/11/2021
Onset Date: 01/12/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data:

Allergies:

Symptoms: aches; muscle pain; low grade fever; enlarged lymphnodes left supraclavicular region; This is a spontaneous report from a contactable other health care professional. A 41-year-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; lot number: EL3246), intramuscular on 11Jan2021 at SINGLE DOSE at left arm for COVID-19 immunization. The patient's medical history was not reported. The patient has no known allergies. Concomitant medications included fluoxetine hydrochloride (PROZAC), bupropion hydrochloride (WELLBUTRIN), fexofenadine hydrochloride (ALLEGRA). The patient had first dose of COVID-19 vaccine on 21Dec2020 intramuscular at right arm. On 12Jan2021, the patient experienced aches, muscle pain, low grade fever, and enlarged lymphnodes left supraclavicular region. The outcome of the events was recovering. The patient did not receive treatment for the events.

Other Meds: PROZAC; WELLBUTRIN; ALLEGRA

Current Illness:

ID: 0973370
Sex: F
Age:
State: FL

Vax Date: 01/05/2021
Onset Date: 01/05/2021
Rec V Date: 01/26/2021
Hospital:

Lab Data: Test Name: temperature; Result Unstructured Data: Test Result: Unknown results.

Allergies:

Symptoms: unrelenting itchiness all over her body for 2 days; soreness at the injection site; overwhelming sleepiness for quite a few hours after the vaccine; tired; This is a spontaneous report from a contactable consumer (patient). An 81-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3246, expiration date: unknown), intramuscular (right upper arm) on 05Jan2021 at 11:45 at a single dose for COVID-19 immunization. Medical history was not reported. There were no concomitant medications. It was also reported that she had 2 shots in polio season in 1952 and did not go back for the booster. The patient had no prior vaccinations (within 4 weeks) following prior vaccinations. The patient had symptoms after the first dose of the COVID-19 vaccine, on 05Jan2021. Symptoms are as follows: soreness at the injection site, overwhelming sleepiness for quite a few hours after the vaccine. On 06Jan2021, the patient then had unrelenting itchiness all over her body for 2 days. The patient wanted to know if she can get the second dose, and if the second dose is stronger. She stated that she used to be 5ft 6in and stated that she still says that and did not want to confess that she is shrinking. She said that she took a 4-hour nap and was still tired and then took another hour nap. About 5 hours later, she was still tired and went to bed and slept until the morning. She stated that she normally goes to bed around 3am anyway and she had plenty of sleep that day. She said that she does not sleep all day and does not fall into a stupor. She received the injection on 05Jan2021. She said that she touched the injection site and she felt the soreness a few hours after receiving the injection. She clarified it was 5-6 hours after receiving the injection. She does not know the date when it went away. She said that she did not touch it again. The patient also said that she does not usually itch anyway herself; the itching went into the next day and was centered around the navel. The patient also said that she is no longer experiencing the symptoms that appeared. The patient also checked temperature with unknown results. The event soreness at the injection site and tired resolved in Jan2021, overwhelming sleepiness for quite a few hours after the vaccine resolved on 06Jan2021 while the event unrelenting itchiness all over her body for 2 days resolved on 07Jan2021.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 134,999

Page last modified: 14 December 2021 10:42pm