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
199,106MODERNA
36,710JANSSEN
5,381PFIZER\BIONTECH
2,555GLAXOSMITHKLINE BIOLOGICALS
1,469UNKNOWN MANUFACTURER
897MERCK & CO. INC.
627SEQIRUS, INC.
112DYNAVAX TECHNOLOGIES CORPORATION
91SANOFI PASTEUR
75NOVARTIS VACCINES AND DIAGNOSTICS
40EMERGENT BIOSOLUTIONS
14PAXVAX
12TEVA PHARMACEUTICALS
12PROTEIN SCIENCES CORPORATION
9PFIZER\WYETH
4BERNA BIOTECH, LTD.
4SMITHKLINE BEECHAM
3INTERCELL AG
1MEDIMMUNE VACCINES, INC.
1CSL LIMITED

COVID19 Lot Number

VAX LOT Total
2S9CL7,949
7,473
2,547
1,506
1,187
1,051
1,049
s0294561,043
866
IMM209861
816
UT7065MA766
657
579
U62828AA563
557
538
U6737AA516
515
S034636506
4F472471
458
P100253275449
444
276563436
429
418
4BH32414
MENVEO404
PP9L5362
UJ446AA337
319
306
290
271
49TM3270
R1B252M253
4F472179
933622147
C5763AA144
CW3116134
3Y7NL126
UNK114
113
ARBA141A105
104
103
96
300057A90
79
1F4EB73
R1B743M62
56
UJ090AA55
51
UH894AB46
45
UNK44
UNK42
42
EJ168638
Unknown36
35
34
32
32
26
el128424
24
A115A22
22
EN620222
21
UNK20
20
19
Z127A19
19
17
JEV18K95E15
12
111798PI12
10
A739088
No batch number8
3333324181078
6
6
TAR356
5
5
U6935AA5
UNK5
4
unknown4
3
2
55RB72
2
2
2
2
2
U7124AA2
JEV18A68E2
2
ABYB05BA1
1
1
1
1
AMVA436A1
1
1
TJ3521
A130A; VIS give1
1
U7140BB1
1
1
SP UP016AA1
1
1808P08802/ESV01
037K20A300,947
EL1284288,578
57,766
1,432

Incidents per State

State Total
82,750
CA62,821
FL38,209
TX36,512
NY34,921
PA23,646
IN23,622
IL20,597
MI19,590
OH19,426
NJ18,413
NC16,769
GA15,932
WA15,351
VA15,234
MA14,876
AZ14,206
MN12,940
MD12,656
CO11,908
WI11,425
MO10,240
TN9,685
OR8,768
KY8,437
CT8,300
SC6,700
OK6,293
AL5,692
LA5,025
IA4,825
KS4,821
UT4,637
NV4,374
NM3,967
AR3,807
ME3,161
NH3,096
NE2,918
MS2,859
ID2,785
WV2,469
HI2,459
PR2,417
MT2,414
RI2,076
DE1,868
AK1,830
VT1,734
DC1,715
ND1,388
SD1,269
WY866
GU118
VI69
AS47
MP29
MH8
XB6
FM4
QM3
XV2
XL1

ID: 1677628
Sex: F
Age:
State: FL

Vax Date: 02/11/2021
Onset Date: 02/12/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: rash; scratching and itching so bad; bruising; This is a spontaneous report from a contactable consumer (patient). A 78-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; lot number and expiration date not reported), via an unspecified route of administration on 11Feb2021 at 13:45 (at the age of 78-years-old) at dose 1, single in the left arm for COVID-19 immunisation. Medical history included heart problems and triple bypass, both about 9 years ago. The patient's concomitant medications were not reported. On 12Feb2021, the patient experienced a rash after receiving the first dose of the Pfizer COVID-19 vaccine. The patient was asking if she should still get the second dose. The patient saw her doctor today for the rash. The patient's doctor saw that the rashes breakout on all of the patient's body. The patient took Benadryl tablet as treatment for the rash. On Sunday, on an unspecified date in 2021, the patient was scratching and itching so bad and was bruising herself. Since the dosage on the label was two tablets for an adult, the patient has taken two tablets each day since then. The patient stated that her rash seems to have new ones and today. In the morning, there seemed to be new ones, mostly on her back and on her front. There were not too many on her arms and legs, but mostly, the rash was on the patient's body. The patient cannot see her back, but her doctor looked at her back and said that there was a lot. The patient said that she was usually not allergic to anything, and has taken a lot of different medications, even trial drugs, and those didn't bother her. The patient received treatment of Benadryl for all the events. Outcome of all the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1677629
Sex: F
Age:
State: MO

Vax Date: 02/16/2021
Onset Date: 02/17/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025L20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: Rash (red spotty) on neck, chest, stomach; Nausea; Body Aches; Headache; This is a spontaneous report from a contactable other healthcare professional (patient). A 31-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EN 5318, Expiration Date: 31May2021), via an unspecified route of administration, administered in left arm on 16Feb2021 13:00 (at the age of 31-year-old) as dose 2, single for COVID-19 immunisation at workplace clinic. Medical history included migraines, dairy allergy and egg whites allergy. intolerance from an unknown date and unknown if ongoing, food allergy from an unknown date and unknown if ongoing. Concomitant medications received within 2 weeks of vaccination included ethinylestradiol, norgestimate (SPRINTEC); propranolol; escitalopram oxalate (LEXAPRO); famotidine (FAMOTIDIN). The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EN5318, Expiration Date: 31May2021), via an unspecified route of administration, administered in left arm on 26Jan2021 08:00 (at the age of 31-year-old) as single dose for COVID-19 immunisation. Patient previously took amoxicillin and experienced allergies. 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 COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. On 17Feb2021, patient experienced nausea, headache and body aches. On 18Feb2021, she had rash (red spotty) on neck, chest and stomach. Patient did not receive treatment in response to the events. Outcome of the event rash (red spotty) on neck, chest and stomach was not resolved and rest all the events were resolve don an unknown date in 2021. No follow-up attempts are possible. No further information is expected.

Other Meds: SPRINTEC; PROPRANOLOL; LEXAPRO; FAMOTIDIN

Current Illness:

ID: 1677630
Sex: F
Age:
State: PA

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

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EL1284
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chest discomfort, Dysphagia, Pain in extremity, Visual impairment

Symptoms: She felt "off' as if she was getting sick/Feelings of being ill; Very fatigued and weak; Very fatigued and weak; Very sore arm; This is a spontaneous report from a contactable nurse reported for a female patient (daughter). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/Lot Number: unknown), via an unspecified route of administration on an unspecified date as dose number unknown, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced she felt off as if she was getting sick/feelings of being ill, very fatigued and weak, very sore arm. Nurse reported that, the afternoon after receiving the second dose of BNT162b2 in her left arm stated that she felt off as if she was getting sick. She felt very fatigued and weak. Her arm was very sore, much more sore than after the first vaccination. She reported that her daughter also had the same reaction as she did, with severe fatigue and feelings of being ill but with no fever and a very sore arm. Event took place after use of product. Outcome of the events was unknown. Information on the lot/batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1677631
Sex: F
Age:
State: PA

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: unknown
Dose Series: UNK
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: Her arm was very sore, much more sore than after the first vaccination; This is a spontaneous report from contactable nurse (patient herself) via Pfizer Sales Representa-tive. A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VAC-CINE, formulation: solution for injection, lot number: unknown, expiry date: unknown) via unspecified route of administration, in left arm on an unspecified date as dose 1, single for covid-19 immunisation. Patients medical history and concomitant medications were not reported. The afternoon after receiving the second dose of BNT162b2 in her left arm she felt "off" as if she was get-ting sick. She felt very fatigued and weak. Her arm was very sore, much more sore than after the first vaccination. She reported that her daughter also had the same reaction as she did, with severe fatigue and feelings of being ill but with no fever and a very sore arm. The next day she had pain in her neck and upper back and a sharp pain in her left axilla. She described the pain as if "someone injected the axilla with a long needle." When she examined the axilla, pressing into her arm pit she reported a sharp pain that radiated down her left arm and wrapped around her thumb. She also reported tingling in her fingers when she explores the axilla. The discomfort has lasted 72 hours after her vaccination. She cannot feel a lump on her axilla, just localized tenderness. The outcome of event for "much more sore than after the first vaccination" was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1677632
Sex: F
Age:
State:

Vax Date: 02/18/2021
Onset Date:
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Name: I had a little temperature of 102; Result Unstructured Data: Test Result:little temperature of 102

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: felt lousy; aches from head to toe; slight fever of 102; lump under her left arm; the worst chills she has had in a long time; This is a spontaneous report from a contactable consumer (patient). A 72-year-old female received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported) via unspecified route of administration on 18Feb2021 (age at the time of vaccination was 72-year-old) as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. Previously the patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported) via unspecified route of administration on an unspecified date (age at the time of vaccination was 72-year-old) as a single dose for COVID-19 immunization. On an unspecified date, the patient experienced felt lousy, aches from head to toe, slight fever of 102, lump under her left arm and the worst chills she has had in a long time. The caller stated she received the second dose of the vaccine yesterday and has felt lousy since yesterday evening. She aches from head to toe, has a slight fever of 102, a lump under her left arm, and the worst chills she has had in a long time, and she still feels kind of bad. Consumer stated, I got my second Covid shot (Clarified as Covid 19 vaccine) yesterday Pfizer and I was feeling warmed. I got to see was I had a little temperature of 102 and I ache from head to toe and I have got a lump under my left arm which was where I got the injection. I was looking at all the literature that was given and it does not say anywhere in there that I can take. Can I take Ibuprofen or acetaminophen or aspirin to get rid some of these thing. I do not want to take something that is going to be wrong, but I like to. When paraphrased the concern, Consumer stated, Absolutely, yes. I can't move and this lump under my left arm I think is like (incomplete sentence). Everything hurts. On an unspecified date, the patient underwent lab and medical procedure which included Body temperature which showed result of little temperature of 102. Outcome of all the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1677633
Sex: F
Age:
State: VA

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

Vax Type: FLUC4
Manufacturer: SEQIRUS, INC.
Vax Name: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT)
Lot: 276563
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chills, Confusional state, Eye inflammation, Headache, Laboratory test

Symptoms: She felt a little sore at the injection site; This is a spontaneous report from a Pfizer-sponsored program COVAX US Support from a contactable female consumer (patient). A female patient of unspecified age received unknown dose of bnt162b2 (Pfizer Covid-19 Vaccine, Solution for injection), via an unspecified route on an unspecified date as a single for covid-19 immunization. The patient medical history and concomitant medications were not reported. On an unknown date, patient felt a little sore at the injection site and just wanted to know if she can take Tylenol to feel better. The clinical outcome of the event was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1677634
Sex: F
Age:
State: FL

Vax Date: 02/12/2021
Onset Date:
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: Caller discovered a red lump and swelling next to the injection site.; Caller discovered a red lump and swelling next to the injection site.; Caller discovered a red lump and swelling next to the injection site.; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number was not reported, expiration date was not reported), via an unspecified route of administration on 12Feb2021 as dose 2, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that, patient received 2nd dose yesterday. Patient discovered a red lump and swelling next to the injection site. Patient asked is that a reason for a concern. The outcome of the events was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1677635
Sex: F
Age:
State: MA

Vax Date: 02/17/2021
Onset Date: 02/18/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: muscle and joint aches primarily in the, shoulders, neck arms, wrists in particular and ankles, and along the spine; muscle and joint aches; generally not feeling well; This is a spontaneous report from a contactable consumer or other non-healthcare professional (patient). A 35-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot Number: EL3247), via an unspecified route of administration, administered in left arm on 17Feb2021 15:00 (age at the time of vaccination was 35 years old) as dose 2, single for covid-19 immunisation. The facility type was other. The medical history included cough variant asthma from an unknown date and unknown if ongoing. Also known allergies were reported as no. The patient's concomitant medications were not reported. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot Number: EL3247), via an unspecified route of administration, administered in left arm on 27Jan2021 15:00 as dose 1, single for covid-19 immunisation. It was reported that no other vaccine was administered in four weeks. The patient had no covid prior vaccination. On 18Feb2021 21:30, the patient experienced muscle and joint aches, muscle and joint aches primarily in the, shoulders, neck arms, wrists in particular and ankles, and along the spine. It was reported that, the onset 28-32 hrs post second dose, muscle and joint aches primarily in the shoulders, neck, arms, wrists in particular and ankles, and along the spine and generally not feeling well. It was reported that the patient first noticed the symptoms of an AE on 18Feb around 9:30pm. She did not realize they were part of an AE until the morning of 19Feb, when they had not improved. The patient was not tested for covid post vaccination. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1677636
Sex: F
Age:
State: NY

Vax Date: 02/13/2021
Onset Date: 02/01/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Name: Weight; Result Unstructured Data: Test Result:Around 170 pounds lbs

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: Whole part of my left face became swelled and very tender to the touch; Whole part of my left face became swelled and very tender to the touch; I was feeling like tingling like if you have eaten something sour; I have a salivary gland clog; swollen lymph node/left side of the salivary gland started to swell; I have a salivary gland clog; swollen lymph node/left side of the salivary gland started to swell; This is a spontaneous report from a contactable Consumer or other non-HCP (patient). A 68-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 13Feb2021 (Lot Number: EL9266; Expiration Date: May2021) (at the age of 68-year-old) as DOSE 1, SINGLE for covid-19 immunisation. Medical history was none. Concomitant medication(s) included Clarithromycin (CLARITIN [CLARITHROMYCIN]) taken for an unspecified indication, start and stop date were not reported. On 17Feb2021, the patient experienced her left side of the salivary gland started to swell and feeling like tingling like if you have eaten something sour, on 18Feb2021, the whole part of her left face became swelled and very tender to the touch and on unspecified date in Feb2021, patient experienced swollen lymph node. The clinical details of the events as follows: She stated that on Saturday 13Feb she received her first dose of the Pfizer covid vaccine and on Wednesday night, her left side of the salivary gland started to swell. Next day it was tender and swollen. She went to the urgent care and they prescribed her antibiotic for it and night at around 10:30, she was eating something, and she was feeling like tingling like if you have eaten something sour and then whole part of her left face became swelled and very tender to the touch. She really did not think it was anything related to the vaccine because, she had the shot five days ago and had no reaction, nothing. She went to the urgent care today, who said she had the Covid shot who was a Nurse Practitioner, who thought that she had a salivary gland clog and she put her on antibiotic (Treatment) and she was talking to her daughter and her daughter said, she just read Pfizer again and swollen lymph node which was her gland is a side effect. Treatment: Consumer stated the only thing, she went to Urgent care and she gave her antibiotic and she actually taken one dose of that antibiotic, which she thought was Amoxicillin. She wanted to know if its ok to take antibiotic before her next dose of the covid vaccine. She wanted to know if it is possible side effects of the vaccine happened 5 days later. She has an ENT appointment on Monday. No Investigation Assessment was provided. This case reported as non-serious. The patient outcome of the events was unknown at the time of this report. No follow-up attempts are possible. No further information is expected.

Other Meds: CLARITIN [CLARITHROMYCIN]

Current Illness:

ID: 1677637
Sex: F
Age:
State: CA

Vax Date: 02/11/2021
Onset Date: 02/01/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J201A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: bad diarrhea side effect after receiving COVID-19 vaccine; This is a spontaneous report from a program. This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN), via an unspecified route of administration on 11Feb2021 as a single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced bad diarrhea side effect after receiving covid-19 vaccine on Feb2021. Outcome of the event was unknown. Information on the lot/ batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1677638
Sex: F
Age:
State: MD

Vax Date: 02/12/2021
Onset Date:
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Vaccination site erythema, Vaccination site pruritus, Vaccination site swelling

Symptoms: injection site feels sore; I feel chilly and numb; I feel chilly and numb; This is a spontaneous report from a contactable consumer or other non hcp (patient) from a Pfizer-sponsored program Support. A female patient of an unspecified age received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on 12Feb2021 at dose 2, single for covid-19 immunisation. Medical history and concomitant medications were not reported. Patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on an unspecified date at dose 1, single for covid-19 immunisation. On an unspecified date in 2021 the patient experienced injection site feels sore, i feel chilly and numb. Verbatim and Event Description: Took a second shot yesterday, the injection site feels sore and I feel chilly and numb. Can I take Tylenol. Outcome of the events was unknown. Information about lot/batch number has been requested. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1677639
Sex: F
Age:
State: TN

Vax Date: 02/13/2021
Onset Date:
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039k20a
Dose Series: 1
Vax Route: SYR
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: nausea; headache; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer reported for herself that. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), via an unspecified route of administration on 13Feb2021 13:30 (Batch/Lot number was not reported) as DOSE NUMBER UNKNOWN SINGLE for covid-19 immunization. The patient medical history and concomitant medications were not reported. on an unspecified date the patient experienced nausea and headache. She wanted to know what to do, and Potential AE realized after call. The event outcome was Unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1677640
Sex: F
Age:
State: TX

Vax Date: 02/06/2021
Onset Date: 02/13/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Blood pressure decreased, Chest pain, Chills, Confusional state, Decreased appetite

Symptoms: dizziness after taking the 2nd dose a week ago/she was dizzy; Her head started spinning; This is a spontaneous report from a contactable consumer or other non hcp (patient reported for herself) from a Pfizer Sponsored Program COVAX US Support. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation solution for injection) via an unspecified route of administration on 06Feb2021 (Batch/Lot number was not reported) as dose 2, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient previously received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on an unspecified date, as single dose for COVID-19 immunization. It was reported by the patient that after receiving the second dose of vaccine a week ago on 13Feb2021 she experienced dizziness, she was dizzy, and her head started spinning. She wanted to know if that is connected to the vaccine. If it is, how long is it expected to last. The outcome of the event was unknown. Information on the lot/batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1677641
Sex: M
Age:
State:

Vax Date: 02/09/2021
Onset Date: 02/01/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20-2A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Dyspnoea, Fatigue, Feeling abnormal, Head discomfort, Headache

Symptoms: cold; feeling sick; This is a spontaneous report from a contactable consumer (patient) received via Pfizer. A male patient of an unspecified age received bnt162b2 (Pfizer-Biontech Covid-19 vaccine), dose 1 via an unspecified route of administration on 09Feb2021 (Batch/Lot number was not reported) as dose 1, single, single for covid-19 immunisation. Medical history included asthma from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. On an unspecified date in Feb2021, the patient experienced cold and feeling sick. He reported that he was feeling sick/felt like he was getting sick before the dose was given. By morning of the dose, he felt better, but "right away, felt under the weather. The patient reported that when he gets sick, it typically turns into bronchitis because he has a history of asthma. Prednisone is typically used for treatment. The patient was prescribed prednisone to take, but he is not taking it at this time because he knows it will decrease immune system and doesn't want to interfere with the vaccine working. The patient stated that he has no fever and loss of taste. The outcome of the events was unknown. No follow-up attempts are possible, information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1677642
Sex: F
Age:
State:

Vax Date: 02/06/2021
Onset Date: 02/06/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Heart rate decreased, Heart rate increased, Hypertension, Injection site pain, Musculoskeletal chest pain

Symptoms: profuse bleeding at injection site; This is a spontaneous case received from a contactable consumer (patient) via Medical Information Team. An 87-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Lot number: EL9262) via an unspecified route of administration in left arm on 06Feb2021, 12:00 (age at vaccination 87-year-old) as single dose for COVID-19 immunisation. Patient medical history includes ongoing blood pressure started on an unknown date, stents on an unspecified date in Sep2020. Concomitant medications include Clopidogrel for blood thinner, Carvedilol, Felodipine, and Olmesartan for blood pressure. Patient historical vaccine includes Flu vaccine on an unknown date for flu immunisation. On 06Feb2021 it was reported as patient received first dose and reports profuse bleeding at injection site for 8 hours. She takes blood thinner, Clopidogrel. The Pfizer COVID-19 Vaccine injection was just a little needle going in. The bleeding was from the injection site and she bled down through her sweater and had to give pressure but she could not get enough pressure on the site. she knew it started a little bit at that point when she got the injection initially; but she was not aware it was going on until a couple or few hours later. She just had a little band-aid that they put on the injection site because it was not a problem at the time they injected her to their or her awareness. Bleeding went on for about 8 hours; and she recovered completely that day as far as she is aware. She has taken the flu injection and something else for surgery, she has never had any kind of reaction like this profuse bleeding. She has been on blood thinner Clopidogrel and never had this profuse bleeding before. The outcome of the event was recovered on 06Feb2021. No follow-up attempts are possible. No further information is expected.

Other Meds: CLOPIDOGREL; CARVEDILOL; FELODIPINE; OLMESARTAN

Current Illness: Blood pressure abnormal; Stent placement placed in the arteries in Sep2020

ID: 1677643
Sex: F
Age:
State: SC

Vax Date: 02/13/2021
Onset Date: 02/01/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Nausea, Pain, Pain in extremity, Paraesthesia oral, Pyrexia

Symptoms: Sore arm; raised knob/Knot and redness at the injection site; bruised; This is a spontaneous report from a contactable consumer (patient, self-reported). A 71-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EN6200 and expiry date: Jun2021), via Intramuscular, in Arm Left, on 13Feb2021 at 11:30 AM (age at vaccination: 71 years), as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. historical vaccine included first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EL9265 and expiry date: May2021), via Intramuscular, in Arm Right, on 27Jan2021 (age at vaccination: 71 years), as a single dose for COVID-19 immunization. The patient did not receive any prior vaccinations within 4 weeks. The patient reported that she received the second shot of the Pfizer covid vaccine last Saturday 13Feb, and she still has a raised knob on an unspecified date in Feb2021, not as red as it was before, was seemingly going the direction of her elbow, and looks bruised. She was looking for information related to these symptoms. The patient stated she hasn't really had any problems with it or side effects. However, at the injection site, she still has a knot. It's starting to look like its bruised going down on her arm. She clarified further she still has a knot there where the shot was injected and it's still red and raised, however it looks like it starting to go down her arm. The patient wanted to know if that was part of the vaccine. She knew it has to come from the shot but was that okay. The patient explained about the second day after receiving the second vaccine, she started to feel her arm get sore on 15Feb2021 and it was kind of red. By the third day, it got a little bigger but she knew that's where they put the medicine into the arm/muscle and everything. The injection site has a knot. When probed for the outcome, the caller explained it's kind of been like this. She started out with nothing, then she developed the knot at the injection site and had some redness and its real sore. She was just thinking by this time, the knot should be going away by now. It looks like it's bruised around the knot and was going down her arm. The events did not require a visit to emergency room or physician office. Outcome of the event raised knob/Knot and redness at the injection site was recovering and for all other events, it was unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained

Other Meds:

Current Illness:

ID: 1677644
Sex: F
Age:
State: MN

Vax Date: 02/15/2021
Onset Date: 02/01/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: DTAPHEPBIP
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: DTAP + HEPB + IPV (PEDIARIX)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data: Test Name: blood pressure; Result Unstructured Data: Test Result:fine; Comments: Her blood pressure is fine, everything is normal.

Allergies:

Symptom List: SARS-CoV-2 antibody test, SARS-CoV-2 test negative

Symptoms: dizzy; not feeling good; itchiness all over; weakness; muscle pain; she felt a little achy to her arm; joint pain; rash; This is a spontaneous report from a contactable consumer. This consumer reported for a 96-year-old female patient (mother). A 96-year-old female patient received bnt162b2 (COMIRNATY, solution for injection Batch/Lot Number: EL9264), via intramuscular route, administered in arm left on 15feb2021 at 2.00 pm as (at the age of 96-years) dose number was 1, single dose for covid-19 immunization. Patient Medical history included internal rash and has trouble with her eyes. She is not really on any medication. The only medication she is on is Lexapro and then she has trouble with her eyes. She mentions she had herpes in her eye and lost vision in her eye. This has been 15 years ago. She is on Vioxx. Reporter mother has been on these medications for a long time, confirming its been more than 2 weeks before getting the vaccine. Her last shot was the flu shot and that was in Aug or Sep, probably Sep. Further it was the high dose of the flu vaccine and her mother got sick from that, however it was nothing that couldn't be controlled. She was sick for a couple days. Otherwise, she has had her regular flu shots now and she is fine. She had no NDC, Lot number or expiry date for the high dose flu vaccine her mother received and got sick from. She believed this was 4 or 5 years ago. She is getting some therapy. Reporter clarifies that her mother has been seeing the dermatologist and they have been giving her light treatments. She has an internal rash so they have been doing that a couple months now. The patient concomitant medications were not reported. On 17Feb2021 the patient felt a little achy to her arm on. On 18Feb2021 she felt dizzy, not feeling good, itchiness all over, weakness, muscle pain and in Feb2021 she experienced joint pain in and rash. Clinical course : on Monday, 15Feb2021, she took her mother in to get the COVID-19 injection. She was fine Monday. Tuesday, she was fine, she stated she felt a little achy, but it was no big deal. Last night and this morning, reporter clarified it has been going for the last couple of days, she has had some muscle pain, joint pain. She did not have any difficulty breathing or any swelling of the face, throat, or issues with her heartbeat. She went over all the symptoms with her mother and there was nothing. However, her mother has a rash, it's nothing there but it itches. She also is having some dizziness and weakness. She stated she doesn't feel 100% but she does feel better. Her mother is currently laying down now. Patient got up this morning and she didn't feel good, so her daughter brought her some juice. Patient told her she was up most of the night. The patient informed her daughter she just felt so weak. She told her she never felt this strange before. However, there is no shortness of breath. Her mother kind of complained about being a bit dizzy, but sometimes that happens to her. She is 96. The caller just doesn't know where the fine line is. She does not not know if this could still be related to the injection. Her mother is pretty much self-quarantined. She has a hard time walking and when she goes out, she uses a wheelchair. The rash first appeared maybe Tuesday night or Wednesday. She states you can't see anything, it just itches. The itching is in her shoulder blades and also in her hip area. Confirms none of her mother's symptoms have required a visit anywhere. Her main concern and question to her mother is are you breathing okay. Her blood pressure is fine, everything is normal. So, she had breakfast this morning and everything like that. Her mother thinks she is feeling better, it just kind of hit her last night. Now, today it seems to be subsiding and everything seems to be getting better, but she doesn't know where the fine line is. Events were reported as non-serious. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1677645
Sex: F
Age:
State: IA

Vax Date: 02/12/2021
Onset Date: 02/01/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: HIBV
Manufacturer: MERCK & CO. INC.
Vax Name: HIB (PEDVAXHIB)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: pain on both arms; upset stomach; leg cramps; This is a spontaneous report from a contactable consumer or other non hcp Pfizer-sponsored program. A female patient of an unspecified age received bnt162b2 (Pfizer Covid-19 Vaccine, Solution for injection, Lot No was not reported), via an unspecified route of administration on 12Feb2021 as 1stdose, single for covid-19 immunisation. The patient medical history was not reported, and concomitant medications were not reported. The patient experienced pain on both arms, upset stomach, leg cramps on Feb2021. Patient is asking if our vaccine is FDA approved. Outcome of the event was unknown. Upon follow-up 12May2021 it was stated that follow-up attempts completed. No further information expected Follow-up (12May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1677646
Sex: M
Age:
State: CA

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

Vax Type: PNC13
Manufacturer: PFIZER\WYETH
Vax Name: PNEUMO (PREVNAR13)
Lot:
Dose Series: UNK
Vax Route:
Vax Site: LG

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: pain after the 1st dose of the vaccine; This is a spontaneous report from a contactable consumer (patient) received from a Pfizer-sponsored program COVAX US Support. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number and Expiration date were not reported), via an unspecified route of administration on an unspecified date as a dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient started to feel pain after the 1st dose of the vaccine. The outcome of the event was unknown. Information on lot/batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1677647
Sex: F
Age:
State: MI

Vax Date: 02/12/2021
Onset Date: 02/13/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: RV1
Manufacturer: GLAXOSMITHKLINE BIOLOGICALS
Vax Name: ROTAVIRUS (ROTARIX)
Lot:
Dose Series: 1
Vax Route: PO
Vax Site: MO

Lab Data:

Allergies:

Symptom List: Blood pressure increased, Chest discomfort, Heart rate increased

Symptoms: She's feeling a little tired; This is a spontaneous report from a Pfizer-sponsored program COVAX US Support. A contactable Female consumer reported for herself. A female patient of an unspecified age received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on 12Feb2021 (Batch/Lot number was not reported) as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced she's feeling a little tired on 13Feb2021. It was reported that caller received the Pfizer Covid-19 vaccine yesterday and wanted to ask if it was okay to take a glass of wine. She was feeling a little tired. The outcome for event was unknown. Follow-up attempts are completed. No further information is expected

Other Meds:

Current Illness:

ID: 1677648
Sex: M
Age:
State: AL

Vax Date: 02/12/2021
Onset Date: 02/01/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: Eh9899
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Lymph node pain, Lymphadenopathy

Symptoms: chills; not feeling well; This is a spontaneous report received from a contactable consumer via Pfizer Sponsored Program COVAX Support. A 72-year-old male patient (husband) received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number was not reported), dose 2 via an unspecified route of administration on 12Feb2021 as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date in Feb2021, patient experienced chills, not feeling well and wanted to know if he can take Tylenol. The clinical outcome of events was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1677649
Sex: F
Age:
State:

Vax Date: 02/10/2021
Onset Date:
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: headache; This is a spontaneous report received from a contactable consumer or other non hcp. A female patient of an unspecified age received 1st dose of bnt162b2 (COMIRNATY,Batch/Lot number was not reported), via an unspecified route of administration on 10Feb2021 as Dose 1,single for covid-19 immunization.The patient medical history and concomitant medications were not reported.The patient experienced headache on an unspecified date.The outcome of the events was unknown.The patient wanted to know if she can take Tylenol because of a headache. Information about the Lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1677650
Sex: F
Age:
State: SC

Vax Date: 01/16/2021
Onset Date:
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chills, Dizziness, Injection site pain, Myalgia, Pyrexia

Symptoms: the pain of the vaccine was better than after the first dose; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 32-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation solution for injection) via an unspecified route of administration on 16Jan2021 (Batch/Lot Number: EK9231) as dose 1, single for covid-19 immunization (at the age of 32-years-old). The patient medical history was not reported. There were no concomitant medications.The patient previously took multivitamin [vitamins nos] and MiraLax (patient stated that she has not taken any medication, even things she used to take those but she has not taken any of those in a while). It was reported that patient received first dose of vaccine and on an unspecified date in 2021 patient experienced the pain and she stated that the pain of the vaccine after second dose which she took on 05Feb2021 was better than after the first dose. Patient stated that she got the product because she was an essential worker, and everyone else at her work had gotten the shot and they were all acting like it was such a great thing. The outcome of the event was unknown. Follow-up attempts are completed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021183644 similar report from same reporter

Other Meds:

Current Illness:

ID: 1677651
Sex: M
Age:
State: NY

Vax Date: 02/12/2021
Onset Date: 02/01/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011L20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: had some pain in left arm where the vaccine was administered; This is a spontaneous report from a contactable consumer (patient) from a Pfizer-sponsored program COVAX US Support. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number and Expiration date was not reported), via an unspecified route of administration, administered in Arm Left on 12Feb2021 as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced had some pain in left arm where the vaccine was administered on Feb2021. Caller just got the 1st dose vaccine the day before this report and had some pain in left arm where the vaccine was administered. Caller asked if he could take 81mg Aspirin and use hot rubs that have methanol content. Clinical outcome of event was unknown. Information on lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1677652
Sex: F
Age:
State:

Vax Date: 01/23/2021
Onset Date:
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: congestion in the sinus area; sore in her arm; This is a spontaneous report from a Pfizer Sponsored Program COVAX US Support from a contactable consumer. A female patient of an unspecified age received bnt162b2 (Formulation: Solution for injection; Batch/Lot number was not reported), dose 1 via an unspecified route of administration on 23Jan2021 as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The caller is due for her 2nd dose tomorrow 14Feb. She is asking if she can take her 2nd dose tomorrow since she has developed little congestion in the sinus area. The caller said after the first dose she had a little sore in her arm. The outcome of the events was unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1677653
Sex: M
Age:
State: OR

Vax Date: 02/17/2021
Onset Date: 02/18/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data: Test Date: 20210218; Test Name: EKG; Result Unstructured Data: Test Result:normal; Test Date: 20210218; Test Name: pulse; Result Unstructured Data: Test Result:a bit lower than normal

Allergies:

Symptom List: Arthralgia, Chills, Headache, Mobility decreased, Myalgia

Symptoms: cold sweats; balance issues/balance was off; a very serious dizzy spell/dizziness; pulse is a bit lower than normal; This is a spontaneous report from a contactable consumer (patient). A 78-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number was not reported) via an unspecified route of administration on 17Feb2021 12:15 (at the age of 78 years old) as dose 1, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced cold sweats, balance issues/balance was off, a very serious dizzy spell/dizziness, pulse is a bit lower than normal on 18Feb2021. Reported as, patient experienced an adverse reaction with the covid vaccine. He had a severe disease spell consisting of cold sweats, balance issues, and dizziness that they had to call (Number). When the paramedics came his EKG read normal but his pulse is a bit lower than normal. On Thursday (18Feb2021), around 10:30 or 11, he got a very serious dizzy spell and cold sweats. Patient states that it was very serious because his balance was off and the dizziness. The patient underwent lab tests and procedures which included electrocardiogram: normal on 18Feb2021, heart rate: a bit lower than normal on 18Feb2021. Outcome of all the events were unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1677654
Sex: F
Age:
State: AZ

Vax Date: 02/18/2021
Onset Date: 02/18/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: she is in such pain; face & neck pain; headache; back pain; shoulder pain; face & neck pain; This is a spontaneous report from a contactable consumer (reporter's husband). A female patient of an unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot number was not reported), Solution for injection, via an unspecified route of administration on 18Feb2021 as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient historic vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot number was not reported), Solution for injection, via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. On 18Feb2021, the patient experienced headache, back, shoulder pain, face & neck pain and she is in such pain. Patient had their 2nd Pfizer vaccine dose yesterday. She was fine up until last night, but she was in such pain this morning and the middle of the night. Caller stated his wife was having a headache, back pain, shoulder pain, and face & neck pain which started last night. Caller enquired about anything that she can take and how soon can she take Tylenol. The outcome of events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1677655
Sex: F
Age:
State: MO

Vax Date: 02/12/2021
Onset Date: 02/01/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: she had just a "slight" arm ache when she tried to raise her arm/little bit of an ache in her arm; bruise; This is a spontaneous report from a contactable consumer (patient). A 68-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EN6200, and Expiration date: Unknown), intramuscular, administered in right arm (she was reported as right-handed) on 12Feb2021 07:30 (at the age of 68-year-old) as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Previously the patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EL3302, and Expiration date: Unknown), intramuscular, administered in left arm on 22Jan2021 (at the age of 68-year-old) for COVID-19 immunization. The patient did not receive any other vaccine (within 4 weeks) since her flu shot which was in late Oct, early Nov, exact date was unknown. It was reported that the patient received both doses exactly 3 weeks apart, on 22Jan2021 and 12Feb2021. After the first vaccine she had no reaction, she could not even feel where the provider injected the shot in her arm. After the second one, on the other arm, "she had just a "slight" arm ache when she tried to raise her arm/little bit of an ache in her arm". She realized when she went to raise her arm, she was like "geez, that hurts". She clarified it did not hurt, but she could feel something. The patient got the second shot at 7:30 am and the ache came in 6 hrs after vaccination (mid-afternoon), it lasted until next morning when she "couldn't feel anymore" at 8 am. This went away probably maybe by 26-28 hours. This ache in her arm was gone by noon the next day. It was nothing. She additionally experienced a sore arm and bruise 68 hours after her 2nd dose was administered, in Feb2021. She heard after the vaccines there would be a feeling and there would be a reaction, she was curious that to assure that her body was "creating a reaction" should she had a reaction. She was hearing everybody else having reactions and that having a reaction means your body was creating antibodies. She was wondering if she had antibodies and was protected. She was asking should she get a test. Investigation assessment was not provided. No further details were provided or obtained. The outcome of the event "she had just a "slight" arm ache when she tried to raise her arm/little bit of an ache in her arm" reported as resolved on 13Feb2021. The outcome of event bruise was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1677656
Sex: F
Age:
State: VA

Vax Date: 02/12/2021
Onset Date: 02/13/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data: Test Name: blood pressure; Result Unstructured Data: Test Result:120/70; Comments: Normally her blood pressure is 120/70.; Test Name: blood pressure; Result Unstructured Data: Test Result:dropped; Comments: As soon as she got off her feet and eliminated the pain, her BP dropped.; Test Date: 20210216; Test Name: blood pressure; Result Unstructured Data: Test Result:high; Comments: The pain caused her blood pressure to go sky high.; Test Date: 20210218; Test Name: blood pressure; Result Unstructured Data: Test Result:120/51; Comments: She had two episodes with her blood pressure last night. Each time lasted a half an hour and went back down to 120/51.; Test Name: Ultrasound; Result Unstructured Data: Test Result:Unknown results; Comments: She has had an ultrasound to check for a deep vein thrombosis. It was assumed to be negative.

Allergies:

Symptom List: Headache, Heart rate increased, Injection site erythema, Injection site pain, Injection site swelling

Symptoms: pain caused blood pressure to go sky high after the second dose; such tremendous pain from my knee to my toes; pains in elbow; This is a spontaneous report from a contactable consumer (patient). An 86-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 2 via an unspecified route of administration on 12Feb2021 (age at vaccination 86-years-old) (Batch/Lot Number: EM9810) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included right knee replacement on Apr2018. Caller reported that she has a history of a knee replacement about 3 years ago, as a result she normally experiences nerve pain from her hip to her knee, breast cancer from Aug2013 to an unknown date, ongoing diastolic heart failure, ongoing macular degeneration, ongoing vitamin d decreased, ongoing reflux and to protect her stomach and ongoing hypothyroidism. Concomitant medication included 200ug levothyroxine sodium (SYNTHROID) (daily), 20mg omeprazole (20 mg, daily (ER 20mg daily), furosemide (40 mg, daily) for diastolic heart failure, spironolactone (12.5 mg, daily (25mg, takes half tab daily) for diastolic heart failure, ascorbic acid, betacarotene, cupric oxide, tocopheryl acetate, zinc oxide (PRESERVISION) (1 daily) for Macular degeneration, vitamin d nos (5000 iU, daily (5,000 units daily) for vitamin D level was low. On 22Jan2021, the patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration at left arm (age at vaccination 85-years-old) (Batch/Lot Number: EK4176) as DOSE 1, SINGLE for covid-19 immunisation and had sore arm and was achy. On 13Feb2021, over the weekend she woke up with pains in her elbow like sticking a needle in it. It lasted for a minute and then it went away. It came and went and then it was gone. She had five episodes of pain in the elbow. On 14Feb2021, her pains in elbow recovered. On 15Feb2021, Monday she had tremendous pain in her right leg from the knee down to her ankle. She was unsure if the pain is related to the vaccine or to the knee replacement. She had an ultrasound to check for a deep vein thrombosis. It was assumed to be negative. They didn't make her wait on the table. She asked if we had any weird side effects. The pain in her right leg varies. On 16Feb2021, the pain caused her blood pressure to go sky high. Normally her blood pressure was 120/70. She was active. She tried to rule out the pain. She had two episodes with her blood pressure last night. Each time lasted a half an hour and went back down to 120/51. As soon as she got off her feet and eliminated the pain, her BP dropped. On 19Feb2021, her pain caused blood pressure to go sky high after the second dose recovered. At the time of this report, the outcome of such tremendous pain from my knee to my toes was unknown and other event outcome was recovered on 14Feb2021 and the event pain caused blood pressure to go sky high was recovered on 19Feb2021. No follow-up attempts are possible. No further information is expected.

Other Meds: SYNTHROID; OMEPRAZOLE; FUROSEMIDE; SPIRONOLACTONE; PRESERVISION; VITAMIN D NOS

Current Illness: Diastolic heart failure; Hypothyroidism; Macular degeneration; Reflux oesophagitis

ID: 1677657
Sex: F
Age:
State: GA

Vax Date: 02/01/2021
Onset Date: 02/01/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data: Test Name: blood work of my A1C; Result Unstructured Data: Test Result:Unknown results; Test Name: HCT; Result Unstructured Data: Test Result:Unknown results

Allergies:

Symptom List: Nausea

Symptoms: knot above her collar bone; like a node just above my collar bone and half inch from my neck and the swelling that was around it; This is a spontaneous report from a contactable consumer (patient). A 68-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration, administered in left arm on Feb2021 (at the age of 68-years-old) as DOSE 2, SINGLE for covid-19 immunisation. The patient medical history included diabetes mellitus and hypertension. The concomitant medication(s) included atorvastatin 10 mg, metformin 1000 mg, hydrochlorothiazide, triamterene (TRIAMTERENE HCTZ) 37.5 mg half per day, pantoprazole 40 mg and mometasone furoate monohydrate (MOMETASONE FUROATE) 15 mcg nasal spray 2 squirts a day. The patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration, administered on an unspecified date (at the age of 68-years-old) as DOSE 1, SINGLE for covid-19 immunisation. The patient reported on Feb2021, next night around 19:00 following vaccination, I noticed like a node just above my collar bone and half inch from my neck and it's still there and the swelling that was around it has gone down from what I can hardly tell swelling was there but the little node as still there. So I need to know what I should do, if that has come from the vaccine and it's on the left side which was the left arm where I got the injection. The patient underwent lab tests and procedures which included glycosylated haemoglobin of blood work AIC with unknown results on unspecified date and HTC with unknown results on an unspecified date. Patient took Tylenol for the event. The outcome of the event was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: ATORVASTATIN; METFORMIN; TRIAMTERENE HCTZ; PANTOPRAZOLE; MOMETASONE FUROATE MONOHYDRATE

Current Illness:

ID: 1677658
Sex: F
Age:
State: KY

Vax Date: 01/30/2021
Onset Date: 01/31/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: UNK
Vax Route: IM
Vax Site: LA

Lab Data: Test Name: A1C; Result Unstructured Data: Test Result:8.2

Allergies:

Symptom List: Injection site pain

Symptoms: skin sensitivity/Skin had this feeling like someone had rubbed fiberglass on her skin where it was prickly and crawly all over, but there was no rash; Severe aches and pains; Headache/ head was just pounding; Severe sore throat; if you think about the size of a hand-towel and put that over her from her breast down to her stomach, that oblong area was just very hot; her blood pressure felt elevated; Fever; This is a spontaneous report from a contactable registered nurse (patient). A 72-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number and Expiry Date were not reported), via an unspecified route of administration on 30Jan2021 around 10:00 or 10:30 as dose 1 single for COVID-19 immunisation. Medical history included hypertension (her blood pressure has been going up, but the doctor said it was under fair control) and type 2 diabetes mellitus (this condition was not under the best control; she thought her last A1C was 8.2 on an unknown date. She was working on getting that under control). The patient's concomitant medications were not reported. It was reported that the registered nurse was the patient who reported this was the first time she has reported this to Pfizer. She previously called a COVID-19 hotline but she doesn't thought they reported it, they just listened to her and referred her to some websites and things. She was administered her first dose of Pfizer COVID-19 Vaccine 30Jan2021. On 31Jan2021 starting Sunday in the early evening, probably around 18:30 she had onset of symptoms: severe sore throat; her blood pressure felt elevated; she had a headache that felt like a headache typical of someone with hypertension, where her head was just pounding; and the symptoms just progressed. She reported if you think about the size of a hand-towel and put that over her from her breast down to her stomach, that oblong area was just very hot. Then patient had skin sensitivity/ her skin had this feeling like someone had rubbed fiberglass on her skin where it was prickly and crawly all over, but there was no rash. Then she had severe aches and pains. Took Tylenol. These events lasted through Thursday on 04Feb2021. She did not get out of bed until Thursday. Her husband had to help her up to the bathroom. She was able to manage to take her medicines and drink fluids. She was very, very concerned about these effects. Her second dose was scheduled for tomorrow, 20Feb2021. No one can tell her what to do. She wants to be vaccinated but feels like what happened to her was dangerous and could do more harm than good. She reported these events were definitely adverse effects, they were not normal. She added that she also had a fever in 2021 but the fever only lasted a couple of days in 2021. She saw a doctor this week. Her family doctor was out of town for 2 weeks so she saw another doctor in his practice who was very, very competent. That doctor said if everything she said was correct he would not get the second injection of Pfizer COVID-19 Vaccine. She asked if these events have ever been heard of before with the Pfizer COVID-19 Vaccine. She asked if there was information on if she should or should not get the second dose of Pfizer COVID-19 Vaccine relative to these events. Seriousness criteria of the events were unspecified. The outcome of the event of Fever was recovered in 2021 and other events was recovered on 04Feb2021. The causality was not provided. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1677659
Sex: M
Age:
State: CA

Vax Date: 02/18/2021
Onset Date: 02/19/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 20210219; Test Name: fever; Result Unstructured Data: Test Result:100.6 Fahrenheit

Allergies:

Symptom List: Injection site induration, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: I had an odd "mole-like" large spot suddenly appear on my left forearm/another similar looking spot has appeared about 3 inches away from the first one; Today I was very lethargic most of the day; chills, achiness, headache, and a fever of 100.6 deg F; chills, achiness, headache, and a fever of 100.6 deg F; chills, achiness, headache, and a fever of 100.6 deg F; chills, achiness, headache, and a fever of 100.6 deg F; This is a spontaneous report from a contactable consumer (patient). A 58-year-old male patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), at an unknown route at right arm on 18Feb2021 at 11:00, (lot number=EN5318) (age at vaccination 58-year-old) as dose 2, single for COVID-19 immunization in the workplace clinic. The patient had known allergies zithromax. The patient medical history included hypertension from an unknown date and unknown if ongoing. The patient had taken 4 hypertension medications in 2 weeks. The patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) at right arm on 28Jan2021 at 02:30 PM (lot number: EN5318) as dose 1, single for COVID-19 immunisation. The patient concomitant medications were not reported. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient was very lethargic most of the day and had chills, achiness, headache and a fever of 100.6 deg F on 19Feb2021 at 6:30 AM and had an odd "mole-like" large spot suddenly appear on my left forearm/another similar looking spot has appeared about 3 inches away from the first one on 21Feb2021. The patient did not received treatment for the events. The event odd "mole-like" large spot suddenly appear on my left forearm/another similar looking spot has appeared about 3 inches away from the first one was not recovered and the outcome of events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1677660
Sex: M
Age:
State: MS

Vax Date: 02/12/2021
Onset Date: 02/01/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011j20a
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Dizziness, Nausea, Pain, Tachycardia

Symptoms: felt muscle twitching; This is a spontaneous report from a Pfizer-sponsored program COVAX Support. A contactable male consumer (patient) of unknown age reported that he received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: unknown) via an unspecified route of administration on 12Feb2021 as dose 1 single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unknown date in Feb2021 the patient felt muscle twitching. The event outcome was unknown. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1677661
Sex: F
Age:
State: NJ

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Date: 2021; Test Name: blood work; Result Unstructured Data: Test Result:Unknown Results

Allergies:

Symptom List: Tremor

Symptoms: received the vaccine in the right arm in which she experienced injection site soreness; pain in my hip joint; I am having pain there, from my hip down to my knees and this is on my right side; This is a spontaneous report from a contactable consumer via medical information team. This female consumer reported for herself. A 70-year-old female patient BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection, Lot Number: EL3306), via unspecified route of administration, in right arm on unspecified date (at the age of 70- year-old) as a dose 2, single and received first dose of BNT162B2 ((PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number: EL0140), via unspecified route of administration on 27Jan2021 in right arm as a dose 1, single for COVID-19 immunization. Patient medical history included blood pressure high and high cholesterol. The concomitant medication of patient was not reported. On unspecified date the patient reported a side effect after receiving both doses of the COVID vaccine. Patient stated that she received the vaccine in the right arm in which she experienced injection site soreness and patient was still experiencing pain in her hip joint, slightly down her right leg and thigh. Patient also reported that she was having pain there, from her hip down to her knees and this was on her right side. Patient stated that she was on hold for 4 hours and wanted to talk to somebody about the vaccine because she got the two doses of vaccination and was on hold from 3 O clock this afternoon. Patient also stated that she read paper and on the side effects, on her right side her hip and her knee it was like she was having pain there, from her hip down to her knees and this was on her right side the side she got the vaccination. The patient underwent lab tests and procedures for blood work, and she dont know it was last week or the week before. Patient received the treatment of baby aspirin (Lot number: 86395886) and stated it didn't even help. The outcome of the events was unknown. No follow-up attempts are possible; No further information is expected.

Other Meds:

Current Illness:

ID: 1677662
Sex: F
Age:
State: KY

Vax Date: 02/02/2021
Onset Date: 02/03/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: back pain/ worsened back pain; arthritis got really bad/worse; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (patient) reported that a female patient of an unspecified age (reported as 76; unit unknown) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot/batch number and expiration date not reported) via an unspecified route of administration on 02Feb2021 as dose 1, single for COVID-19 immunisation. The patient's medical history included arthritis. Concomitant medications were not reported. The patient received 1st dose of vaccine on 02Feb2021. She said, the following day she woke up with back pain. Patient said, "I got up with it being pretty painful". Patient was evaluated by HCP and was prescribed meloxicam (on 09Feb2021). She said her arthritis got really bad/worse after the 1st dose of the vaccine (2021). She had 2nd dose schedule for Tuesday and was asking if she can continue taking her meloxicam. Reported worsened back pain after the first dose. Has taken medications a week after. Outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1677663
Sex: F
Age:
State: FL

Vax Date: 02/06/2021
Onset Date: 02/01/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: UNK
Manufacturer: UNKNOWN MANUFACTURER
Vax Name: VACCINE NOT SPECIFIED (NO BRAND NAME)
Lot:
Dose Series: UNK
Vax Route: SYR
Vax Site: UN

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site induration, Injection site pruritus, Injection site swelling, Myalgia

Symptoms: sicker; headache; Couldn't get out of bed; chills; muscle ache; dizziness; sweats; nausea; bone/joint pain; bone/joint pain; This is a spontaneous report from a contactable consumer (patient) via Medical information team, Pfizer-sponsored program COVAX US SUPPORT and Pfizer-sponsored program Corporate (Pfizer) Social Media Platforms. An 82-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 06Feb2021 at the age of 82 years old (Batch/Lot number was not reported) as SINGLE DOSE for COVID-19 immunisation. Medical history included pulmonary fibrosis, trouble breathing (wear oxygen all the time), "pressure reducer for my eye", cardiomyopathy, lung cancer, lung surgery for cancer and poor vision all from an unknown date; COVID-19 from 01Apr2020, (hospitalized for 6 days and I was on 'Remdesivir' (not clarified) and all, everything they gave you). Concomitant medications included levothyroxine, acetylsalicylic acid (BABY ASPIRIN), dexamethasone (DEXALONE), spironolactone, cetirizine hydrochloride (ZYRTEC), clonazepam, hydroxyzine, trazodone, famotidine, amitriptyline, pirfenidone (ESBRIET), esomeprazole sodium (NEXIUM), lovastatin and clopidogrel; all taken for an unspecified indication, start and stop date were not reported. The patient stated, "I had a bad reaction. I woke up the next day and I was really very sick, probably for 6 days. I had the Covid like symptoms. I had the headache, dizziness, chills, sweats, nausea, muscle pain, bone/joint pain. I had everything that I had, but of course not to the extent. Thursday I finally could get up and stay up. I'm not sure. Do I have enough antibodies to not receive the second dose? What does Pfizer recommend? Will the blood test or antibodies show either? If I should or not get the second dose? I thought I read something yesterday that Pfizer announced one shot would be efficient". The patient got the first dose last 05Feb and she mentioned that after getting the first dose she was very ill, she had chills and muscle ache. The patient further stated, "I am 83. I have pulmonary fibrosis and cardiomyopathy and I have had lung cancer. I had the Pfizer vaccine on 06Feb, first shot of Pfizer COVID-19 Vaccine. Before we had it, I also had COVID on April 1st and I was hospitalized for 6 days and I was on 'Remdesivir' (not clarified) and all, everything they gave you. I was not on a ventilator. Anyway, we talked to the doctor before I got my vaccine and told them that I had COVID. His advice was to take the vaccine and to see what my reaction was. If it was minor, have the second shot, if it was major don't have the second shot. The day after, I woke up, I had chills, I had sweats, I never had a fever even during COVID, I had muscle and joint aches, I had nausea, I had a headache, I was dizzy. I had it all and I couldn't get out of bed from Sunday to Thursday. My question is do you advice that I take the second vaccine which I am due to have a week from today." The outcome of events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: LEVOTHYROXINE; BABY ASPIRIN; DEXALONE [DEXAMETHASONE]; BUMETANIDE; SPIRONOLACTONE; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; CLONAZEPAM; HYDROXYZINE; TRAZODONE; FAMOTIDINE; AMITRIPTYLINE; ESBRIET; NEXIUM [ESOMEPRAZOLE SODIUM]; LOVASTATIN; CLOPIDOG

Current Illness:

ID: 1677664
Sex: F
Age:
State: NY

Vax Date: 01/29/2021
Onset Date: 01/29/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Cough, Limb discomfort, Pain, SARS-CoV-2 test positive

Symptoms: face flushed which patient described that it felt like her face stung (had pain); face flushed which patient described that it felt like her face stung (had pain); This is a spontaneous report from a non-contactable consumer (patient). A 66-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN5318), via an unspecified route of administration, administered in the right arm on 29Jan2021 10:30 (at the age of 66-year-old) as single dose for covid-19 immunisation. Medical history included asthma, high blood pressure, high cholesterol, sulfa allergy and cobalt allergy. The patient was not pregnant at the time of vaccination. The patient did not have other vaccine in four weeks and did not have covid prior to vaccination. Concomitant medication included lisinopril (MANUFACTURER UNKNOWN); atorvastatin (LIPITOR [ATORVASTATIN]); azelastine (MANUFACTURER UNKNOWN); fluticasone (MANUFACTURER UNKNOWN); alendronate sodium (MANUFACTURER UNKNOWN); trazodone (MANUFACTURER UNKNOWN); gabapentin (MANUFACTURER UNKNOWN); montelukast sodium (SINGULAIR). The patient experienced face flushed which patient described that it felt like her face stung (had pain) on 29Jan2021 10:30. It was reported that no treatment was given in response to the events. The patient was not tested for covid post vaccination. The patient recovered from the events on an unspecified date. No follow-up attempts are possible. No further information is expected.

Other Meds: LISINOPRIL; LIPITOR [ATORVASTATIN]; AZELASTINE; FLUTICASONE; ALENDRONATE SODIUM; TRAZODONE; GABAPENTIN; SINGULAIR

Current Illness:

ID: 1677665
Sex: F
Age:
State: IL

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: paranoid; This is a spontaneous report from a contactable consumer (patient) via Pfizer Sponsored Program Support. A female patient of an unspecified age received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number, Expiration date and NDC number was not reported), via an unspecified route of administration, administered in arm on an unspecified date as dose 1, single for COVID-19 immunisation. The patient medical history was not reported. Concomitant medication(s) included methotrexate taken for an unspecified indication, start and stop date were not reported. On an unspecified date, when patient took her vaccine, there was no serum injected on her. It was just a single and a quick prick on her arm. Patient does not know if that was because she got the Pfizer or just being paranoid. The event was reported as non-serious by the patient. Patient asked if we had info on how the vaccine should be administered and asked if she can get the vaccine at a different vaccination site. Patient saw her Rheumatologist Thursday and she said that if patient was taking Methotrexate that it was recommended that she stop it before she had her COVID-19 Vaccine. Patient reported she already had one dose of Pfizer COVID-19 Vaccine injection and was due to have her second dose of Pfizer COVID-19 Vaccine on Wednesday. Patient was trying to find out if she had to stop taking the Methotrexate and if so, how long after taking the second dose of Pfizer COVID-19 Vaccine until she can restart Methotrexate. The outcome of the event was unknown. Follow-up attempts completed. No further information expected.

Other Meds: METHOTREXATE

Current Illness:

ID: 1677666
Sex: F
Age:
State:

Vax Date: 02/17/2021
Onset Date: 02/17/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 011J20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pain, Injection site swelling

Symptoms: Moderate/severe injection site pain with active movement peaked at 9-15hr mark; Elevated temperature 99.5-100.0; Insomnia; This is a spontaneous report from a non-contactable other healthcare professional (patient). A 31-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EM9810), via an unspecified route of administration, administered in the left arm on 17Feb2021 11:30 (at the age of 31-year-old) as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient was not pregnant at the time of vaccination. The patient did not have other vaccine in four weeks and did not have covid prior to vaccination. On 17Feb2021 at 05:00 pm, the patient experienced moderate/severe injection site pain with active movement peaked at 9-15hr mark and elevated temperature at 99.5-100.0 in the evening, responsive to 325mg acetaminophen (TYLENOL). The patient also experienced insomnia on the night of 17Feb2021, and no treatment was given in response to the event. The events were reported as non-serious. The patient was not tested for covid post vaccination. The patient recovered from all the events on an unspecified date. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1677667
Sex: F
Age:
State: MS

Vax Date: 02/11/2021
Onset Date:
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot: EK9231
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Chills, Feeling cold, Feeling hot, Myalgia, Pain

Symptoms: sore arms; This is a spontaneous report from a contactable consumer or other non-healthcare professional from a Pfizer-sponsored program COVAX US Support. A female patient of an unspecified age received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 2 via an unspecified route of administration on 11Feb2021 (Batch/Lot number and Expiry date was not reported) as DOSE 2, SINGLE for covid-19 immunization. The patient medical history was not reported. Concomitant medications included acetaminophen taken for an unspecified indication, start and stop dates were not reported. The patient previously received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number and Expiry date was not reported) for covid-19 immunization. On an unspecified date in 2021, the patient experienced sore arms. The reporter stated that she had her 2nd dose of vaccine yesterday (11Feb2021) while waiting for more than two and half hours on the line, she decided to take a medicine called acetaminophen. She later found out that taking medicine before having the vaccine is the wrong thing to do, she said that she did not feel any side effects aside from having sore arms. She was concerned if the second shot will be diminished or if she can take another second dose because of the medicine she took prior to taking the 2nd dose. The clinical outcome of the event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds: ACETAMINOPHEN

Current Illness:

ID: 1677668
Sex: M
Age:
State:

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

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data: Test Name: Blood sugar; Result Unstructured Data: Test Result:High

Allergies:

Symptom List: Pain in extremity

Symptoms: high blood sugar levels; This is a spontaneous report from a contactable consumer or other non healthcare professional. A 73 year old male patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced high blood sugar levels on an unspecified date with outcome of unknown. The patient underwent lab tests and procedures which included high blood glucose. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1677669
Sex: M
Age:
State: CT

Vax Date: 02/19/2021
Onset Date: 02/20/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 2
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Abnormal behaviour, Adverse reaction, Anger, Asthma

Symptoms: Tiredness; Headache; Muscle and joint aches; Muscle and joint aches; Feeling unwell; This is a spontaneous report from a contactable consumer (patient). A 59-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration, administered in Arm Left on 19Feb2021 13:00 (Batch/Lot Number: EL3247) as dose 2, single at 59 years old for COVID-19 immunization at a workplace clinic. Medical history included hypertension and hyperlipidaemia from an unknown date. Concomitant medications included hydrochlorothiazide, triamterene (DYAZIDE) and atorvastatin both taken for an unspecified indication, start and stop date were not reported. The patient previously took Zoloft and experienced drug allergy. The patient previously received the first dose of bnt162b2 (lot number: EL3247) on 29Jan2021 at 01:30 PM on the left arm at 59 years old for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 20Feb2021, the patient experienced tiredness, headache, muscle and joint aches, and was feeling unwell. The reporter assessed the events as non-serious. The events did not result in death or life threatening condition, hospitalization, disability, or congenital anomaly. No treatment was received. The outcome of the events was recovering. Follow-up attempts completed. No further information expected.

Other Meds: DYAZIDE; ATORVASTATIN

Current Illness:

ID: 1677670
Sex: F
Age:
State: PA

Vax Date: 02/11/2021
Onset Date: 02/11/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 039K20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Consciousness fluctuating, Crying, Dry skin, Epistaxis, Headache

Symptoms: Massive headache/migraine, tiredness, apathy, body aches; Massive headache/migraine, tiredness, apathy, body aches; Massive headache/migraine, tiredness, apathy, body aches; Massive headache/migraine, tiredness, apathy, body aches; Massive headache/migraine, tiredness, apathy, body aches; This is a spontaneous report received from a contactable consumer or other non-health care professional (patient). A 29-years-old non-pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: E28982), via an unspecified route of administration, administered in Arm Left on 11Feb2021 09:15 (at the age of 29-years-old) as dose 2, single for COVID-19 immunisation. Medical history included atopic dermatitis, anxiety, OCPD (Obsessive-compulsive personality disorder), Known allergies: Nickel, Known allergies: Grass/trees from an unknown date and unknown if ongoing. Concomitant medications included sertraline (SERTRALINE), dupilumab (DUPILUMAB), ethinylestradiol, levonorgestrel (AVIANE), ergocalciferol (VIT D) taken for an unspecified indication, start and stop date were not reported. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: E13302) via an unspecified route of administration, administered in Arm Left on 21Jan2021 10:30 AM (at the age of 29-years-old) as dose 1, single for COVID-19 immunisation. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, was the patient did not diagnosed with COVID-19. Since the vaccination, did not patient been tested for COVID-19. The patient experienced massive headache/migraine, tiredness, apathy, body aches on 11Feb2021 14:00. The outcome of the events was reported as not recovered. Follow-up (14May2021): Follow-up attempts completed. No further information expected.

Other Meds: SERTRALINE; DUPILUMAB; AVIANE; VIT D

Current Illness:

ID: 1677671
Sex: F
Age:
State:

Vax Date: 02/04/2021
Onset Date: 02/04/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025J20A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Hypotonia, Lethargy, Respiratory rate decreased, Screaming, Skin warm

Symptoms: Muscle pain; tiredness; This is a spontaneous report from a non-contactable consumer or other non hcp. A 40-years-oldnon-pregnant female patient received first dose of bnt162b2 (covid 19 vaccine, formulation: solution for injection, Batch/Lot Number: EL3247), via an unspecified route of administration, administered in Arm Right on 04Feb2021 (at the age of 40-years-old) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included from an unknown date and unknown if ongoing Other medical history: No. The patient had no allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient did not receive any other medications within 2 weeks of vaccination. The patient's concomitant medications were not reported. On 04Feb2021, the patient experienced muscle pain, tiredness. Therapeutic measures were taken as a result of muscle pain (myalgia), tiredness (fatigue).The outcome of the events was recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1677672
Sex: M
Age:
State: NY

Vax Date: 02/08/2021
Onset Date: 02/11/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 026LZOA
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: Lympnode under left arm is swollen.; Some pain; This is a spontaneous report from a contactable consumer. This 72-year-old male consumer reported that he received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EL9264) via an unspecified route of administration on 08Feb2021 (at 72-year-old) on left arm as dose 2, single for COVID-19 immunization. The medical history of the patient included penicillin allergy and hypertension. It was mentioned that patient did not receive any other vaccine in four weeks, did not have covid prior vaccination and was not tested for covid post vaccination. The concomitant medications included indapamide, amlodipine and finasteride all taken at unknown dose, start date and stop date unknown) taken for unknown indication. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot number: EL 3747) via an unspecified route of administration on 17Jan2021 at 01:30 PM (at 72-year-old) on left arm as dose 1, single for COVID-19 immunization. On 11Feb2021 at 06:00 Am the patient noticed swelling and exposed vein and experienced lymphadenopathy and pain. No treatment was received, and patient had not recovered. Follow-up attempts were completed. No further information was expected.

Other Meds: INDAPAMIDE; AMLODIPINE; FINASTERIDE

Current Illness:

ID: 1677673
Sex: F
Age:
State: NJ

Vax Date: 02/05/2021
Onset Date: 02/08/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: SYR
Vax Site: LA

Lab Data: Test Date: 20210210; Test Name: rapid COVID test; Test Result: Negative

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: tired; Chills; Achy; little dizzy; little nausea; This is a spontaneous report from a contactable consumer (Patient). A 46-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EM9809), dose 1 via an unspecified route of administration, administered in Arm Left on 05Feb2021 at 14:15 (Age at vaccination: 46 years) as dose 1, single for covid-19 immunisation. Medical history included ongoing migraine. Additional Information for Other Conditions was 20 years. Concomitant medications included botulinum toxin type a (BOTOX) taken for migraine from 04Feb2021 to 04Feb2021; Dexamethasone taken for migraine from 06Feb2021 to Feb2021. she only took it for 3 days and that dosing pack has been completed. She was trying to break the migraine cycle and hence she was having. Prior vaccinations within 4 weeks were None. The patient experienced tired, chills, achy, little dizzy, little nausea on 08Feb2021. she was a teacher who got her first vaccine on Friday, 05Feb2021. She was tired over the weekend and more flu like on Tuesday. She went to take a COVID test that was negative on the rapid test and then it was sent off. Her question, since her neurologist gave the steroid and she took Botox for her migraines, could that effect the efficacy of the vaccine. She didn't think about the fact she was prescribed a steroid and that she had been given Botox by her neurologist after the vaccine. The school nurse wanted her to call and report this since she was still experiencing side effects on the 5th and 6th day after the shot. The shot was given on the 05Feb2021 at 2:15pm. The tiredness started Sunday the 08Feb2021, she was feeling got worse and she was feeling pretty lethargic most of Tuesday evening and Tuesday night into Wednesday. It was better now but still ongoing. Chills- This started Sunday, they were better. Achy- This started Sunday but the worst of it was Tuesday and Wednesday. A little dizzy and nausea- this started Sunday and was less today. Rapid tests were done Wednesday, 10Feb2021 which was negative; the test was sent away for the PCR and she should get results back in 3-5 days. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 10Feb2021. The outcome of the events was recovering. Follow-up (12May2021): Follow-up attempts completed. No further information expected.

Other Meds: BOTOX; DEXAMETHASONE

Current Illness: Migraine

ID: 1677674
Sex: F
Age:
State: CA

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

Vax Type: COVID19
Manufacturer: PFIZER\BIONTECH
Vax Name: COVID19 (COVID19 (PFIZER-BIONTECH))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data: Test Date: 20210130; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptom List: Back pain, Cold sweat, Headache, Nausea, Vomiting

Symptoms: 3 days later had facial; The night of vaccine was unable to move my entire left side untill next morning and just felt as if got ran over with body aches; The night of vaccine was unable to move my entire left side untill next morning and just felt as if got ran over with body aches. 3days later had facial; This is a spontaneous report from a contactable other hcp reported for herself. A 44-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number and Expiration date was not reported), via an unspecified route of administration, administered in Arm Left on 15Jan2021 14:00 (at the age of 44-years-old) as DOSE 1, SINGLE for covid-19 immunisation. Patient was not pregnant at the time of vaccination. Medical history included none. Had no known allergies. The patient's concomitant medications were not reported. No other vaccine in four weeks and in two weeks. No covid prior vaccination and covid was tested post vaccination. The patient experienced the night of vaccine was unable to move her entire left side until next morning and just felt as if got ran over with body aches on 15Jan2021 14:00, 3 days later had facial on 18Jan2021. The patient underwent lab tests and procedures which included covid-19 (Rapid antigen nasal swab): negative on 30Jan2021. No treatment received for AE. Clinical outcome of event was recovered on an unspecified date. Information on lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1677675
Sex: F
Age:
State: KS

Vax Date: 02/02/2021
Onset Date: 02/02/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 025j20-2A
Dose Series: 1
Vax Route: IM
Vax Site: LA

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: still have pain in left arm; This is a spontaneous report from a contactable consumer (reported for herself). A 44-years-old female non-pregnant patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration, administered in arm left on 02Feb2021 at 10:00 (at the age of 44-years-old) as dose 1, single for covid-19 immunisation at workplace clinic. Medical history included ongoing hypersensitivity (Known allergies: Yes). Concomitant medication included estradiol (ESTRADIOL) taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 02Feb2021, the patient experienced still have pain in left arm. The reporter stated the event result in Doctor or other healthcare professional office/clinic visit. No treatment was given for the events. The outcome of the event was resolving. Follow-up attempts completed. No further information expected.

Other Meds: ESTRADIOL

Current Illness: Allergy (Known allergies: Yes.)

ID: 1677676
Sex: F
Age:
State: MA

Vax Date: 02/11/2021
Onset Date: 02/11/2021
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot:
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Chills, Diarrhoea, Fatigue, Feeling abnormal, Headache

Symptoms: Headache; nausea; Soreness at the injection site; This is a spontaneous report from a contactable consumer. A 43-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection. Batch/Lot Number: EL3247), dose 1 via an unspecified route of administration, administered in left arm on 11Feb2021 at 11:45 (at the of the 43-years-old) as DOSE 1, SINGLE for COVID-19 immunization. Medical history reported as none. No concomitant medication was reported. The patient was not pregnant at the time of vaccination. Patient had no known allergies. No other vaccine in four weeks. Other medications in two weeks: Birth Control. No COVID prior vaccination. On 11Feb2021 at 20:00, the patient experienced headache, nausea and soreness at the injection site. No treatment received for the adverse event. No COVID tested post vaccination. The outcome of the events were recovered on 2021. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1677677
Sex: F
Age:
State:

Vax Date: 02/09/2021
Onset Date:
Rec V Date: 09/07/2021
Hospital:

Vax Type: COVID19
Manufacturer: MODERNA
Vax Name: COVID19 (COVID19 (MODERNA))
Lot: 037K20A
Dose Series: 1
Vax Route: IM
Vax Site: RA

Lab Data:

Allergies:

Symptom List: Hot flush, Myalgia, Nausea, Tension headache

Symptoms: the vaccinated area as being swollen; This is a spontaneous report from a Non-contactable consumer (patient). A 81-years-old female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: Unknown), via an unspecified route on 09Feb2021 as dose 1, single in the left arm for covid-19 immunisation. The patient medical history included she suffered a stroke in Feb2020 (affected left side mobility), contracted COVID last April and fully recovered in early May. She is taking medications for diabetes, high blood pressure, cholesterol, thyroid and gout sometimes. The patient concomitant medications were not reported. On unspecified date, the patient experienced the vaccinated area as being swollen but manageable. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am