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**
PLEASE CHECK BACK SOON
Download the files above while you wait.







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: 1673118
Sex: F
Age: 42
State: CA

Vax Date: 04/13/2021
Onset Date: 04/18/2021
Rec V Date: 09/04/2021
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: Kidney infection; very anxious and started to feel panic; This spontaneous case was reported by a consumer and describes the occurrence of KIDNEY INFECTION (Kidney infection) in a 42-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 039AZLA or L:039AZlA) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Anxiety. Concomitant products included VITAMINS NOS for an unknown indication. On 13-Apr-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Apr-2021, the patient experienced KIDNEY INFECTION (Kidney infection) (seriousness criterion medically significant) and ANTICIPATORY ANXIETY (very anxious and started to feel panic). The patient was treated with ALPRAZOLAM for Anxiety, at an unspecified dose and frequency. At the time of the report, KIDNEY INFECTION (Kidney infection) had resolved and ANTICIPATORY ANXIETY (very anxious and started to feel panic) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was withdrawn on an unknown date. Concomitant products also included Supplements for an unknown indication. Treatment information included unspecified Antibiotics for kidney infection for 14 days. Patient stated that she was not sure of what happened or if her defenses went down. Company Comment: Very limited information regarding the event Kidney Infection has been provided at this time. Further information has been requested. There is at least a timely relationship between the event and the vaccination date. The event Anticipatory Anxiety is rather related to the patient?s medical history of anxiety.; Sender's Comments: Very limited information regarding the event Kidney Infection has been provided at this time. Further information has been requested. There is at least a timely relationship between the event and the vaccination date. The event Anticipatory Anxiety is rather related to the patient?s medical history of anxiety.

Other Meds: VITAMINS NOS

Current Illness:

ID: 1673119
Sex: F
Age:
State: MI

Vax Date: 08/14/2021
Onset Date: 08/14/2021
Rec V Date: 09/04/2021
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: feels weak; nausea; wasn't feeling right; chills; within 15 minutes of shot felt high for about an hour after; This spontaneous case was reported by a consumer and describes the occurrence of ASTHENIA (feels weak), EUPHORIC MOOD (within 15 minutes of shot felt high for about an hour after), NAUSEA (nausea), CHILLS (chills) and FEELING ABNORMAL (wasn't feeling right) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 002F21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 14-Aug-2021, the patient experienced EUPHORIC MOOD (within 15 minutes of shot felt high for about an hour after). On 16-Aug-2021, the patient experienced ASTHENIA (feels weak), NAUSEA (nausea) and CHILLS (chills). 16-Aug-2021, the patient experienced FEELING ABNORMAL (wasn't feeling right). On 14-Aug-2021, EUPHORIC MOOD (within 15 minutes of shot felt high for about an hour after) had resolved. At the time of the report, ASTHENIA (feels weak), NAUSEA (nausea), CHILLS (chills) and FEELING ABNORMAL (wasn't feeling right) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product was not provided by the reporter. Treatment information was not provided.

Other Meds:

Current Illness:

ID: 1673120
Sex: U
Age:
State: MA

Vax Date:
Onset Date: 08/17/2021
Rec V Date: 09/04/2021
Hospital: Y

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: Vomiting, and the vomit had visible blood cloths; This spontaneous serious Safety Report was received by Agency on 18-AUG-2021 and forwarded to Agency on 20-AUG-2021 from a health care professional. A 2-month-old patient, with an unknown medical history, had been vaccinated with Vaxelis (dosing number and batch number unknown) on an unspecified date for prophylaxis. The following co-suspect vaccinations were reported: Rotateq and Prevnar 13. On 17-AUG-2021, the patient experienced vomiting, and the vomit had visible blood clots. The patient was admitted to the hospital and was hospitalized for one day on an unknown date. The action taken with Vaxelis was unknown. The outcome of the event was resolved on an unspecified date. The reporter assessed the causal relationship between Vaxelis and the reported event of vomit had visible blood clots as not related. Further information is expected. Company comment: Haematemesis was assessed as serious (hospitalization). Haematemesis is unlisted for Vaxelis, as per the Agency. Considering the current knowledge of the vaccine and the existence of alternative explanations (co-suspect vaccinations administered the same day), the causal relationship between Vaxelis and Haematemesis is assessed as not related. This single individual case safety report does not modify the benefit/risk balance of this product. Therefore, no change in the label or other measures is recommended at this time. However, the company will continue to monitor all respective reports received and, based on cumulative experience, will re-evaluate the available evidence on an ongoing basis.; Sender's Comments: Haematemesis was assessed as serious (hospitalization). Haematemesis is unlisted for Vaxelis, as per the Agency. Considering the current knowledge of the vaccine and the existence of alternative explanations (co-suspect vaccinations administered the same day), the causal relationship between Vaxelis and Haematemesis is assessed as not related. This single individual case safety report does not modify the benefit/risk balance of this product. Therefore, no change in the label or other measures is recommended at this time. However, the company will continue to monitor all respective reports received and, based on cumulative experience, will re-evaluate the available evidence on an ongoing basis.

Other Meds:

Current Illness: Prophylaxis

ID: 1673121
Sex: M
Age:
State: KY

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

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

Lab Data: Test Name: Pain scale; Result Unstructured Data: Test Result:5/10; Comments: headache pain is 5/10

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: headache for 7 days; This consumer reported for a 35-year-old male patient (husband) that: A 35-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Lot number and Expiry date was not reported), dose 1 via an unspecified route of administration on an unspecified date (age at vaccination was 35-year-old) as dose 1, single dose for covid-19 immunisation. The patient medical history was not reported. The patient concomitant medications were not reported. Caller states her husband received the Pfizer Covid vaccine. On an unspecified date, the caller's husband had a headache for 7 days since 1st vaccine dose. He states that headache goes away with a pill and then comes back. The headache pain is 5/10. Asking, when should he go to the emergency room and how long will the headache last. Caller calling on behalf of her husband who reported headaches after the first dose of Pfizer Covid 19 vaccine. Stated that she wanted to know if this is something to be expected after first dose. Agent stated that she was provided with Medical Information department phone number. Clarified that she wanted to know is it regular to have a headache after the first one or does she have to go emergency room. The patient underwent lab tests and procedures which included pain assessment: 5/10, headache pain is 5/10 on an unspecified date. Treatment received for the event. Outcome of the event was not recovered. Information on lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1673122
Sex: F
Age:
State: CA

Vax Date: 07/18/2021
Onset Date: 07/18/2021
Rec V Date: 09/04/2021
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: Injection site erythema, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: scared it can be an allergic reaction; this morning it is a little swollen, her left eye; Headache; night her eye kind of hurt, it felt like a stye coming; night her eye kind of hurt, it felt like a stye coming; crying; scared; This is a spontaneous report from a contactable consumer (reported for herself). A 27-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, lot number: unknown) via an unspecified route of administration, administered in arm left on 18Jul2021 11:30 (age at vaccination was 27-year-old) as dose 2, single for covid-19 immunisation. Vaccine was not administered at military facility. None other additional vaccine was administered on same date of the Pfizer suspect. The patient medical history was not reported. There were no concomitant medications. Previously, the patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot Number: Unknown), via an unspecified route of administration, administered in arm left on 26Jun2021 14:00 (age at vaccination was 27-year-old) as dose 1, single for covid-19 immunisation. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. On 18Jul2021, the patient was crying as was scared after the second dose of vaccination. On 18Jul2021, evening the patient developed left eye pain. The patient states that on 18Jul2021, night her eye kind of hurt, it felt like a stye coming and she thought that's weird. On 19Jul2021, morning (7:00) when the patient woke up with little swelling to her left eye. The patient also had headache on the 19Jul2021. On an unknown date, the patient states that she googled it and feels it could be normal but was scared it can be an allergic reaction. She wants to know if she should expect this or if it's an allergic reaction. The patient did not visit emergency room and physician office. The outcome of the events was unknown. Information about lot/batch number 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: 1673123
Sex: F
Age:
State: OH

Vax Date: 04/02/2021
Onset Date: 04/23/2021
Rec V Date: 09/04/2021
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: slight nausea; menstruation cycles have been significantly heavier; closer in frequency; more discomfort than usual; This is a spontaneous report from a contactable consumer or other non hcp. A 50-years-old non pregnant 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 02Apr2021 10:00 age at vaccination 50 years old (Batch/Lot Number: EW0150) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included asthma, Known allergies: Zithromax polymenorrhoea from 2018 to an unknown date. Concomitant medication(s) included levocetirizine dihydrochloride (XYZAL) taken for an unspecified indication, start and stop date were not reported. The patient previously took zithromax and experienced drug hypersensitivity. The patient did not had COVID prior vaccination and did not have COVID tested post vaccination. The patient did not received other vaccine in 4 weeks. On 23Apr2021 After the first dose, slight nausea, subsided after a few hours. Since the shots, my menstruation cycles have been significantly heavier, closer in frequency (3 weeks instead of 4) with more discomfort than usual. Considering that patient 50 years old, her periods were slowing down since 2018. The patient did not received treatment for the events. Outcome of the event nausea was recovered on unspecified date of 2021 while other events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: XYZAL

Current Illness:

ID: 1673124
Sex: M
Age:
State: AZ

Vax Date: 04/08/2021
Onset Date: 04/01/2021
Rec V Date: 09/04/2021
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: intestinal cramps in the large intestine that has been persistent for over 2 months that gets worse when I eat; debilitating pain; lost 20 lbs; This is a spontaneous report from contactable consumer (patient) via the Regulatory Authority. A 51-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration, administered in arm left on 08Apr2021 13:30 (lot numbers: EW0150 also reported as EN6205; expiry date: unknown) at the age of 51-years-old, as dose 1, single, for COVID-19 immunisation. Medical history included reactive arthritis from food poisoning. The patient had no known allergies. The patient was not diagnosed with COVID prior vaccination. The patient did not receive other vaccines within four weeks prior to COVID vaccination. The vaccine was administered in a Public Health Clinic/Veterans Administration facility. Concomitant medications included ibuprofen, acetaminophen, and gabapentin, and more (unspecified). On 24Apr2021, the patient experienced intestinal cramps in the large intestine that has been persistent for over 2 months that gets worse when he eats. It manifests in the corners of the intestine and can cause debilitating pain. He had a weekend of "normal" reactions then intestines started cramping 2 weeks after that. He had lost 20 lbs since April and shows no signs of slowing down. The patient did not receive treatment for the events. The events resulted in: Doctor or other healthcare professional office/clinic visit. The patient has not been tested for COVID-19 since vaccination. Outcome of the event lost 20 lbs was unknown, while for the other events was not recovered.

Other Meds: Ibuprofen; Acetaminophen; Gabapentin

Current Illness:

ID: 1673125
Sex: U
Age:
State:

Vax Date: 05/05/2021
Onset Date: 05/01/2021
Rec V Date: 09/04/2021
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: my left arm hurt for about 2 days; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender 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 in Arm Left on 05May2021 as single dose for COVID-19 immunisation. Medical history included at the tender age of 40 (unspecified units), diagnosed with chickenpox. The patient had itching and discomfort on the chest and throughout the body. The patient concomitant medications were not reported. The patient previously received shingle shots for immunization. It was reported that 20 years later after chicken pox, the patient heard about shingle shots. Patient learned that people who have had chickenpox carried the same "virus" and decided to get vaccinated. As the pharmacist gave the injection, the patient felt a brief itching sensation, exactly the same location where the patient had the chickenpox, mainly on the chest and all over the body. That lasted only a few minutes and then disappeared. On 05May2021, the patient received first vaccination in left arm. About 8 hours after the vaccination (May2021), left arm hurt for about 2 days and that was all the patient experienced. Outcome of event was unknown. The lot number for the vaccine, [BNT162B2] was not provided and will be requested during follow-up.

Other Meds:

Current Illness:

ID: 1673126
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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: Abdominal pain, Chills, Sleep disorder

Symptoms: ulnar neuropathy; Nerve and muscle problem in my right hand; My lively hood depend on my hand. I am a pianist; This is a spontaneous report received from a contactable consumer, the patient. A patient of unspecified age and gender received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: FA6780), Solution for injection, via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. The patient medical and concomitant medications were not reported. On an unspecified date, the patient experienced nerve and muscle problem in right hand, ulnar neuropathy and he reported that lively hood depend on my hand. i am a pianist. Consumer stated, I have absolute muscle problem and I am a pianist. I went to the regular doctor so; I don't have the exact diagnosis yet but its looks like the ulnar neuropathy. When paraphrased the above concern, consumer sated, It's not muscle, its nerve and muscle problem in my right hand after the first shot. My doctor said it's most likely ulnar neuropathy (Consumer was unsure hence not captured as event) after the vaccine. Consumer stated, I do require a medical assistance because my lively hood depend on my hand. I am a pianist. The outcome of events was unknown.

Other Meds:

Current Illness:

ID: 1673127
Sex: M
Age:
State: MO

Vax Date: 07/30/2021
Onset Date: 07/30/2021
Rec V Date: 09/04/2021
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: vaccine was not diluted; received his first dose of the Pfizer BioNTech Covid 19 vaccine today 30Jul2021 but the vaccine was undiluted; This is a spontaneous report from a contactable nurse. This Nurse reported for a 58-year-old male patient who received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at the age of 58-years-old, via an unspecified route of administration, administered in Deltoid Right on 30Jul2021 (Batch/Lot Number: FA6780; Expiration Date: 26Aug2021) as dose 1, 0.3 ml single (at the age of 58) for COVID-19 immunization. The patient no medical history and no concomitant medications. The patient had no prior vaccination. The administered vaccine was undiluted. Vaccination facility type was workplace clinic. The outcome was unknown. Amendment: This follow up is being submitted in order to update the narrative Follow-up (23Aug2021): New information reported from a contactable nurse includes: medical history and vaccination details. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1673128
Sex: U
Age:
State:

Vax Date: 07/01/2021
Onset Date: 07/01/2021
Rec V Date: 09/04/2021
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: My whole arm hurts it doesn't feel like it's getting better; My fingers are like I got to be say numb and hard to move, like I move it and it just feels so unnatural; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (BNT162B2, Solution for injection, Batch/Lot number was not reported, expiration date: unknown), dose 2 via an unspecified route of administration on an unspecified date in Jul2021 as single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Historical vaccine, the patient received first dose BNT162B2, dose 1 on an unspecified date as single for COVID-19 immunisation. On an unspecified date in Jul2021 the patient's whole arm hurted, it didn't feel like it's getting better and fingers were like patient got to be say numb and hard to move, like if patient move it and it just felt so unnatural. Outcome of the event patient's whole arm hurted, it didn't felt like it's getting better was not resolved and patient's fingers were like, patient got to be say numb and hard to move, like if patient move it and it just felt so unnatural 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: 1673129
Sex: U
Age:
State:

Vax Date: 04/23/2021
Onset Date:
Rec V Date: 09/04/2021
Hospital:

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

Lab Data: Test Name: Blood test; Result Unstructured Data: Test Result:Medical testing blood is fine; Comments: everything has come out clear; Test Name: CAT Scan; Result Unstructured Data: Test Result:clear; Comments: everything has come out clear; Test Name: EMG; Result Unstructured Data: Test Result:Clear; Comments: everything has come out clear; Test Name: MRI brain; Result Unstructured Data: Test Result:Unknown

Allergies:

Symptom List: Rash, Urticaria

Symptoms: Tremors; I can't walk; I can't properly walk or hold myself upright; I had persecution in my muscles in my upper body and lower body; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EX3294) via an unspecified route of administration on 23Apr2021 as DOSE 1, SINGLE for COVID-19 immunisation. The patient medical history was not reported. Concomitant medication(s) included vortioxetine hydrobromide (TRINTELLIX). On an unspecified date in 2021, a week later patient stated that I got tremors and I can't walk, I can't properly walk or hold myself upright and I wanted to know if there are common cases like this. I can go upright, I just can't walk properly or hold myself, but I can't support my body, climb upstairs, I can't go upstairs. So I did all my testing. I got all my medical testing blood is fine, EMG, MRI, CAT Scan and I am doing a brain MRI tomorrow, but everything has come out clear and the only difference is 12Apr2021 my psychiatrist added 5mg of Trintellix and then on 23Apr2021, I have my vaccination that's the only difference that I did before I had persecution in my muscles in my upper body and lower body. Upon follow-up (24Aug2021), patient questioned do you know how many people have this adverse events, is there a place where I can read about this adverse events, how many reports do you have about people taking Pfizer's vaccine who cannot walk and which are the most common adverse events. At the time of this report, the outcome of all the events was unknown. No follow-up attempts possible. No further information expected. Follow up (24Aug2021): New information was received from a contactable consumer. This consumer reported in response to Non-HCP letter via telephonic follow-up activity that included addition of clinical information. No follow-up attempts possible. No further information expected.

Other Meds: TRINTELLIX.

Current Illness:

ID: 1673130
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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: muscle problems in one of his legs and one of his arms; This is a spontaneous report from a contactable consumer or other non hcp (patient's mother). A male patient of unknown age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: unknown, expiration date: unknown), via an unspecified route, on an unknown date as DOSE NUMBER UNKNOWN, SINGLE for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The reporter stated my son is experiencing muscle problems in one of his legs and one of his arms. I think he got Pfizer as well, but I am not sure. You are coming out with a follow up shot but it makes me very uncomfortable getting it. It is a little bit frightening not knowing what is causing this. On an unknown date, patient was reported experiencing muscle problems in one of his legs and one of his arms. The outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1673131
Sex: F
Age:
State: NY

Vax Date: 07/31/2021
Onset Date: 07/31/2021
Rec V Date: 09/04/2021
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: Fever; Body aches; Headache; Chills; Left arm pain; This is a spontaneous report from a contactable consumer (patient). A 31-years-old non-pregnant female patient received second dose of bnt162b2 (BNT162B2, solution for injection), via an unspecified route of administration, administered in Arm Left on 31Jul2021 08:00 (Batch/Lot Number: EW0217) (at the age of 31-years-old) as SINGLE for covid-19 immunization and administered at School. It was reported that known allergies as no and other medical history as no. Historical vaccine included first dose of bnt162b2 (BNT162B2, solution for injection), via an unspecified route of administration, administered in Arm Left on 10Jul2021 08:00 (Batch/Lot Number: EW0217) (at the age of 31-years-old) as SINGLE for covid-19 immunization. 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 COVID-19 vaccine. Also, the patient did not receive any other medication within two weeks. The patient noticed that her 1st dose and 2nd dose have the same lot number and she wants to know if it's normal to have the same lot number for the 1st and 2nd dose. On 31Jul2021 at 21:00 patient experienced fever, body aches, headache, chills and left arm pain. The reporter considered the events as non-serious as no hospitalization is reported. The patient did not received any treatment. The outcome of all the events was recovering. 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: 1673132
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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: Pain; Fever; numbness on right side of shoulder and then going down now the area is expanding; This is a spontaneous report from a contactable consumer. This consumer (patient's husband) reported for a female patient (reporter's wife) of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number: unknown), via an unspecified route of administration on an unknown date in 2021 as dose number unknown, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced pain, fever and numbness on right side of shoulder and then going down now the area is expanding. The 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.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202100994036 same reporter/ AE/ drug, different patient;US-PFIZER INC-202100993856 same reporter/ AE/ drug, different patient

Other Meds:

Current Illness:

ID: 1673133
Sex: F
Age:
State:

Vax Date: 07/28/2021
Onset Date: 07/28/2021
Rec V Date: 09/04/2021
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: Had a persistent metallic taste in her mouth; This is a spontaneous report from a contactable consumer or other non hcp. A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection; Batch/Lot number was not reported), via an unspecified route of administration on 28Jul2021 as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On 28Jul2021 the patient experienced had a persistent metallic taste in her mouth. She is asking if this side effect is common and /or reported by other patients. Outcome of events was unknown. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1673134
Sex: F
Age:
State: LA

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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: Body temperature; Result Unstructured Data: Test Result:99.6; Test Name: Body temperature; Result Unstructured Data: Test Result:100.8

Allergies:

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

Symptoms: Low cough; Not feeling good; Wasn't feeling good; I ran 99.6 fever; I am still, I am running 100.8 fever; Bad headache; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 60-years-old female 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 in left arm on an unspecified date as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient reported that she received the first shot on Thursday, it was the 29th, and was perfectly healthy. The patient got the shot and Saturday night on the 31st, she started with low cough and not feeling good and then yesterday, the patient ran 99.6 fever, had a bad headache and wasn't feeling good. Patient reported feeling better today but was still running 100.8 fever. The patient underwent lab tests and procedures which included body temperature: 99.6 and body temperature: 100.8 on unspecified date. Patient took Tylenol and Ibuprofen as treatment for event. The outcome of the event not recovered. Information on Batch/Lot number requested.

Other Meds:

Current Illness:

ID: 1673135
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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: sharp pain come up into in her leg for about five hours; has bulging veins in that area; This is a spontaneous report from a contactable consumer (patient) via medical information team. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EW0217, Expiration Date: 30Sep2021), dose 1 via an unspecified route of administration on an unspecified date as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient reported that about half an hour after first dose of the Pfizer Covid 19 Vaccine she noted sharp pain come up into in her leg for about five hours and has bulging veins in that area. Patient asked if this was in the range of muscle and joint pain or was there anything to keep an eye out for or be wary of. She states she does not know if these were normal side effects or not. The outcome of events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1673136
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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: Sore arm; This is a spontaneous report from a Pfizer sponsored program from a contactable consumer (patient). A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number was not reported) dose 1 via an unspecified route of administration on an unspecified date as dose 1, single and dose 2 via an unspecified route of administration on an unspecified date (Lot number was not reported) as dose 2, single for COVID-19 immunisation. The patient's medical history and concomitant medication was not reported. On an unspecified date the patient experienced sore arm. Both shots were of Pfizer's. He did not have any reaction other than a sore arm for maybe the next day. No side effects so far. So, he had wait to until something happens, this type of thing has got him worried. The clinical outcome of the event was unknown. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1673137
Sex: F
Age: 23
State: CA

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

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

Lab Data: I have not had any. These changes are uncomfortable but not bad enough to where I feel the need to see a doctor

Allergies: N/A

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

Symptoms: Several hours after I got my second shot, I began spotting blood even though my period was not expected for another 17 days. Since the vaccine, my periods have been heavier, I've experienced intense nausea, and I have had more painful cramps.

Other Meds: N/A

Current Illness: N/A

ID: 1673138
Sex: M
Age: 59
State: MO

Vax Date: 08/01/2021
Onset Date: 08/14/2021
Rec V Date: 09/04/2021
Hospital: Y

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: MRI. CAT and blood work done at the hospital. Follow up included a hearing test. Was diagnosed with Sudden Idiopathic Soundineural Hearing Loss. Labyrinthitis

Allergies: Sulfa

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

Symptoms: On 8/14/21 my ears felt like pressure was building up inside the canal. At 3:00 I exit my vehicle and while at home my left ear proceeded to get worse. Within 3 hours I lost complete hearing in that ear.

Other Meds: Warfarin, Simivastatin, sotolol, Lisinopril

Current Illness:

ID: 1673139
Sex: F
Age:
State: CT

Vax Date: 06/29/2021
Onset Date: 06/29/2021
Rec V Date: 09/04/2021
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: 2021; Test Name: CBC normal; Result Unstructured Data: Test Result:Everything was fine; Test Date: 2021; Test Name: 2 lyme tests; Result Unstructured Data: Test Result:Everything was fine; Test Date: 2021; Test Name: COVID-19 antibody test; Result Unstructured Data: Test Result:Positive

Allergies:

Symptom List: Unevaluable event

Symptoms: pain; This is a spontaneous report from a contactable consumer (patient herself). A 79-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EY0584, Expiry Date: Unknown), via an unspecified route of administration, administered in Arm Left on 29Jun2021 as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications were none. Patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EW0182 and Expiry Date: Unknown), via an unspecified route of administration, in arm left on 04Jun2021 11:00 as dose 1, single for COVID-19 immunisation and experienced with pain was excruciating, Chills and Fever, No appetite, Occasionally feels flushed and Neck, Upper Arm, Thigh Pain. It was reported that, she was scheduled to get her second dose of the COVID Vaccine on 25Jun2021. Due to her symptoms going on at that time she did not get it on that date. She felt well enough to get it on 29Jun2021. On 29Jun2021, patient experienced pain. The patient underwent lab tests and procedures which included full blood count normal was everything was fine, 2 Lyme tests on her was negative, resistance test with her arms and legs, CBS was everything was fine on these tests and SARS-COV-2 antibody test was positive on an unspecified date in 2021. Patient took Tylenol for the pain, but that Tylenol never helps her with pain anyway. She said that the doctor ordered Percocet (combination of Oxycodone and Acetaminophen), as one tablet every 6 hours on the 29Jun2021 to take around the clock for three days. She mentioned that there was a Product Complaint for Tylenol and Percocet, which did not help with pain. The outcome of events was not recovered.

Other Meds:

Current Illness:

ID: 1673140
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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: tinnitus; This is a spontaneous report from a contactable consumer. This consumer (patient's wife) reported for male patient (reporter's husband). A male patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot/ batch number unknown), via an unspecified route of administration on unspecified date as DOSE NUMBER UNKNOWN, SINGLE for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The reporter stated that her husband has tinnitus and his started four days after the vaccine. The outcome of event was unknown. The lot number for the vaccine, [BNT162B2], was not provided and requested during follow up.

Other Meds:

Current Illness:

ID: 1673141
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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: dizziness/she has a friend who is going through something very similar; Vision disorientation/she has a friend who is going through something very similar; ringing in her ears/she has a friend who is going through something very similar; pains in her face/she has a friend who is going through something very similar; anxiety/she has a friend who is going through something very similar; depression/she has a friend who is going through something very similar; This is a spontaneous report from a contactable consumer (patient's friend). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) 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 dizziness, vision disorientation, ringing in her ears, pains in her face, anxiety and depression. At the time of this report, the outcome of event was unknown. The lot number for the vaccine was not provided and will be requested during follow up. F/U (PRD/SRD 25aug2021): Follow-up activities closed: Batch/lot number not available.

Other Meds:

Current Illness:

ID: 1673142
Sex: F
Age:
State:

Vax Date: 08/02/2021
Onset Date: 08/01/2021
Rec V Date: 09/04/2021
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: Injection site pain; Injection site pain which is swelling, red, and hot; Injection site pain which is swelling, red, and hot; Injection site pain which is swelling, red, and hot; They both don't have energy to cook or anything and are sleeping a lot.; They both don't have energy to cook or anything and are sleeping a lot.; They are in a fog and can't think/Feel like they've been run over by a car; This is a spontaneous report from a contactable consumer (patient's daughter) via Medical Information team. An 84-year-old female patient (reporter's mother) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: FA7484; Expiration Date: 30Sep2021, NDC 59267-1000-02), dose 2 via an unspecified route of administration, administered in right arm on 02Aug2021 (at the age of 84-year-old) as 0.3 mL single for covid-19 immunisation. Medical history included pacemaker, fall from 13Feb2021. The patient's concomitant medications were not reported. Historical Vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot Number: EW0181, expiration date 30Aug2021, NDC number: 59267-1000-02) dose 1 via an unspecified route of administration on 12Jul2021 (at the age of 84-year-old) as 0.3 mL single for covid-19 immunisation. The patient had nothing with the first one, she was just tired and sluggish and worn out all a week. This started the day of the vaccine and lasted a week or so, she didn't even want to cook or eat. This improved then she got second dose. Since receiving second doses, patient have been experiencing "injection site pain which was swelling, red, and hot" on 02Aug2021. Her mother's site "was really hot" and "looks like the size of a baseball". Duration of pain at the injection site after Dose 2 was 2.5 days. They want to know if these reactions are normal and how to treat. Asked what if the reaction last longer than 2 days. The patient's looks like a baseball on her arm. The patient's arm is so hot she could fry an egg on her arm. The patient's arm did not bleed when she took the Band-Aid off. In Aug2021, she felt she had been run over by a car. She does not have energy to cook or anything and sleeping a lot. The patient feels like she was in a fog and can't think in Aug2021. The patient's arm was red and very very hot. The redness started right away. Outcome of the events injection site pain which was swelling, red, and hot was not recovered; for other events was unknown. Follow up information completed.no further information expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202100999212 Same reporter/product, similar event, different patient

Other Meds:

Current Illness:

ID: 1673143
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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 Name: fever; Result Unstructured Data: Test Result:102

Allergies:

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

Symptoms: 102 fever; Sick for 2 days; This is a spontaneous report from Pfizer-Sponsored Program. This is a spontaneous report from a contactable consumer (patient's mother). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection), dose 2 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as DOSE 2, SINGLE for COVID-19 immunisation. The patient's medical history included illness from an unknown date and unknown if ongoing, reported that the patient as a baby had always got sick when got vaccines. The patient's concomitant medications were not reported. The patient's historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection), 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. On an unspecified date, the patient experienced 102 fever, and was sick for 2 days. The patient underwent lab tests and procedures which included body temperature: 102 on an unspecified date. The caller stated that her daughter, when the patient got her vaccine, she did not think this had anything to do with it, but her second dose, she had a 102 fever, she was sick for 2 days. The patient recovered from the event sick for 2 days and the outcome for the event 102 fever was unknown. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1673144
Sex: F
Age:
State:

Vax Date: 08/04/2021
Onset Date: 08/04/2021
Rec V Date: 09/04/2021
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: her arm is sore at the injection site; This is a spontaneous report from a non contactable consumer (Patient). A 72-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration on 04Aug2021 as DOSE 1, SINGLE for covid-19 immunisation (at the age of 72 years). Medical history and patient's concomitant medications were not reported. On 05Aug2021 the patient had experienced her arm is sore at the injection site. It was reported that when she did the shot, it was wonderful and she could barely feel anything. After a while, it was sore and also reported that they scheduled her for another shot in two weeks for 25Aug2021. She would like to know when is the latest she can get the second dose. She will be out of town and wants to know if it needs to be done in 2 months, 3 months, 5 months, or whenever is the time frame she would need to have it done in or does she have to schedule another one. She did not wish to provide a mailing address or email and did not wish to complete report. She requested to be transferred to have her question answered. The clinical outcome was unknown. Information on the lot/batch number has been requested

Other Meds:

Current Illness:

ID: 1673145
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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 complaints of fever; This is a spontaneous report from a contactable consumer or other non-HCP (patient mother) via Medical Information Team. A 22-year-old female patient received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number-UNKNOWN) via an unspecified route of administration on an unspecified date as dose 2, single (at the age of 22-years-old) for COVID-19 immunization. Patient medical history and concomitant medications were not reported. Historical vaccine included BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- UNKNOWN) via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. The patient experienced complaints of fever on an unspecified date. The outcome of event was unknown. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1673146
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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:

Allergies:

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

Symptoms: muscle pain with both doses; This is a spontaneous report from a contactable consumer or other non hcp. A 56-years-old male patient received first and second dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection) via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. Caller stated that her 56-year-old husband (patient) had complaints of muscle pain with both doses of the Pfizer Covid-19 vaccine on an unspecified date. The outcome of event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1673147
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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: Nausea

Symptoms: periods became very irregular; This is a spontaneous report from a contactable consumer (Patient) via Pfizer-sponsored program. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number and Expiry date was not reported), via an unspecified route of administration on an unspecified date, as dose number unknown, single for COVID-19 immunization. The patient medical history and concomitant medications was not reported. On unspecified date, the patient experienced periods became very irregular. The outcome of the 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:

ID: 1673148
Sex: F
Age:
State:

Vax Date: 08/03/2021
Onset Date: 08/03/2021
Rec V Date: 09/04/2021
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: Injection site pain

Symptoms: Hard knot, swelling, and redness at injection site/ it felt hard in that spot; hard knot, swelling, and redness at injection site; hard knot, swelling, and redness at injection site; hurt a little more, she has more soreness; This is a spontaneous report from a contactable consumer. This female consumer (patient) reported for herself that: A female patient of unspecified age had received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EW0178, Expiration date ??-AUG-2021), via an unspecified route of administration, administered on left arm on 03AUG2021 at single dose for COVID-19 immunisation. Patient previously took the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EW0178) via an unspecified route of administration on 13Jul2021 at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. After first dose patient had didn't have too much of a reaction maybe a little soreness on Jul2021. After 2nd dose on 03Aug2021, patient had experienced did hurt a little more, she has more soreness but throughout the day she noticed a knot, it felt hard in that spot it felt hard in that spot. Yesterday she noticed that in the area it looks like it was getting swollen like a big mosquito bite that spreads when you scratch it. She iced it yesterday and it still is like that today. She didn't have a reaction the 1st time but she did with the 2nd. Do they put something different in there the 2nd time She was concerned. At the time of reporting, the outcome of the events were not recovered. Description of complaint: Caller reporting AEs following the 1st and 2nd dose of the Pfizer COVID vaccine asked if they put something different in there the 2nd time? She is concerned since she did not have this side effect with the 1st dose. Probed for NDC, lot number and expiry date and caller does not see the NDC or expiry date on the COVID vaccination record card for the 1st dose and doesn't see an NDC for the 2nd dose. Therapy start date populated as the date for the caller's first COVID vaccine and the therapy stop date populated as the date for the caller's second COVID vaccine. Populated 2nd dose lot and expiry date within formal fields since caller's main concern was after the 2nd dose. Caller confirms that both doses have the same lot number.

Other Meds:

Current Illness:

ID: 1673149
Sex: U
Age:
State: CA

Vax Date: 07/14/2021
Onset Date: 07/24/2021
Rec V Date: 09/04/2021
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: Injection site induration, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: fatigue; Joint aches; This is a spontaneous report from a contactable consumer (patient). A 63-year-old patient of an unspecified gender received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), intramuscular, administered in Arm Left on 14Jul2021 afternoon (age at vaccination 63-years-old) (Batch/Lot Number: EW0180) as single dose for COVID-19 immunization. Medical history included hypothyroid from an unknown date. The patient had no medical history at time of vaccine or w/in 3 mo of vaccine. Concomitant medication included levothyroxine sodium (LEVOTHYROXINE) taken for hypothyroid from an unspecified start date and ongoing. The patient did not receive any prior vaccination. Patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), intramuscular, administered in Arm Left on 23Jun2021 afternoon (age at vaccination 63-years-old) (Batch/Lot Number: EW0217) for COVID-19 immunization and experienced minor headache, swollen eyelids and eye puffiness. On 24Jul2021 afternoon, the patient experienced fatigue, joint aches. The patient did not receive any treatment for the events. Outcome of the events was recovered. Follow-up attempts are completed. No further information is expected.

Other Meds: LEVOTHYROXINE [LEVOTHYROXINE SODIUM]

Current Illness:

ID: 1673150
Sex: M
Age:
State:

Vax Date: 07/22/2021
Onset Date:
Rec V Date: 09/04/2021
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: intermittent feeling in his heart; fevers; chills; fatigue; muscular pain; eye twitching; This is a spontaneous report from a contactable consumer or other non-healthcare professional (patient) via medical information team. A 40-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number was not reported), via an unspecified route of administration on 22Jul2021 as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date in 2021, the patient experienced intermittent feeling in his heart, fevers, chills, fatigue, muscular pain, eye twitching. It was reported that the patient received the 1st dose of the Pfizer COVID-19 Vaccine on 22Jul2021. Afterwards the patient reported of having had some of the side effects. The patient reported that he also had different things that he does not see listed on the information sheet. He stated he had fevers, chills, fatigue, muscular pain and then the day after the vaccine he had eye twitching. Also the twitching happens all the time but then he reported an intermittent feeling in his heart that was similar to the what it feels like when you have the chills. The patient reported of having a feeling of the chills but in his heart. This was reported to be an intermittent occurrence. The patient reported that he had a side effect after the first dose of the vaccine and enquired if he should get the second dose. The patient had an appointment next Thursday with his HCP to address his concerns he had experienced post vaccination of dose one. The patient reported that he had an upcoming appointment with his HCP regarding his concerns noted next Thursday, however this was the same day that he was also scheduled to receive his 2nd dose of the vaccine and he was concerned there will not be time to address these concerns and was concerned that he will not have time or have the proper guidance he wanted in regards to getting the second dose of the vaccine. Patient would like to know if we have more information on these 2 side effects that he has experienced that do not seem to be listed on the document he has. The 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: 1673151
Sex: F
Age:
State: NC

Vax Date: 08/03/2021
Onset Date: 08/03/2021
Rec V Date: 09/04/2021
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: Tremor

Symptoms: My arm is still, I mean its still, it is swollen; It is still sore; It is still sore like still red; This is a spontaneous report from a contactable consumer (patient herself). A 68-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EW0191), via an unspecified route of administration administered in Arm Left on 03Aug2021 at 11:30 (age at vaccination was 68 years old) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included cholesterol, which was ongoing and stroke in Apr2021. Concomitant medications included acetylsalicylic acid (BABY ASPIRIN) and atorvastatin calcium (AVASTATIN) taken for blood cholesterol. The patient reported I got my first shot yesterday and yesterday afternoon (03Aug2021), it caused my arm sore and it looks like it's just sore a little red around it. She stated my arm is still, I mean its still, it is swollen and I put a ice pack on it and it is still sore like still red. So, can you tell me for this what I can do to heal it. The only thing I was trying to find out was just what else I need to do? Do I need to take Ibuprofen or what I need to do? It caused my arm sore and it looks like it' s just sore a little red around it. No treatment was received by the patient. The outcome of all the events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds: BABY ASPIRIN; AVASTATIN

Current Illness: Cholesterol (Verbatim: Cholesterol)

ID: 1673152
Sex: F
Age:
State: PA

Vax Date: 08/05/2021
Onset Date: 08/05/2021
Rec V Date: 09/04/2021
Hospital:

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

Lab Data: Test Date: 2021; Test Name: Swab of throat for strep; Result Unstructured Data: Test Result:Unknown

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: her arm is sore post vaccination; This is a spontaneous report from a Regulatory Authortity . A contactable consumer or other non HCP (patient) reported that a 77-year-old female patient received bnt162b2 (BNT162B2, Formulation; Solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 05Aug2021 11:10 (Batch/Lot Number: EW0179) as DOSE 1, SINGLE (at the age of 77-year-old) for covid-19 immunisation. Medical history included ongoing asthma (since 3 or 4 years) and sore throat issue from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. The patient did not have any family medical history relevant with event. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient not received other product. The patient experienced her arm is sore post vaccination on 05Aug2021 at 11.10. The patient asked if she could apply ice to help alleviate the soreness. The patient had question as if she gets a headache can she take Tylenol of extra strength. The patient did not visit emergency room or physician office. It was reported that patient could have not hit incorrectly, and she felt sore right away. The patient doesn't have much time as she needs to call her primary care doctor at 16.00 PM. It was reported that patient had a sore throat and needs to have an endoscope done. She went to the throat doctor and had this problem for some time predating the vaccination; she thinks it was allergies and dripping down throat. The patient underwent lab tests and procedures which included swab of throat for Strep: unknown on an unknown date of 2021. The outcome of the event was reported as not recovered. No follow-up attempts needed. No further information expected.

Other Meds:

Current Illness: Asthma (since 3 or 4 years.)

ID: 1673153
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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: the patient is shaking really bad/I got the shivers until a little while about an hour ago I start shaking/I shake the whole body; the patient is shaking really bad/I got the shivers until a little while about an hour ago I start shaking/I shake the whole body; Leg pain/her legs are bothering her really bad/arm pain; back pain; This is a spontaneous report from a contactable consumer (patients' sister) and two consumers. A 80-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection) via an unspecified route of administration on an unspecified date (Batch/Lot number: Not Provided) as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. It was reported that the caller was calling on behalf of her sister who was from out of town visiting the caller. Her sister got the Pfizer vaccine yesterday who was the patient was shaking really bad, her legs are bothering her really bad. The patient got on the line to explain what was going on. More concerned about the shaking wanting to know if it was a side effect of COVID-19 vaccine. First dose last night around 8'clock I believe I took it and then I got the shivers until a little while about an hour ago I start shaking like a leaf. Leg pain, back pain, arm pain. But the shakes, do you have reports someone shake like this I shake the whole body on an unspecified date. I'll go to a urgent care. Caller clarifies she was referring to the Pfizer COVID-19 vaccine. The caller wants to know if those are side effects? The caller states she did read the reports and she didn't read anything about the shakes. Caller declines to complete a report at this time, requesting immediate transfer stating she can't stand it no more. The outcome of the events was unknown. Follow-up attempts are completed. No further information is expected; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1673154
Sex: F
Age:
State:

Vax Date: 07/13/2021
Onset Date: 07/01/2021
Rec V Date: 09/04/2021
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: Had a little shoulder soreness; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received first dose of bnt162b2 (BNT162B2, solution for injection), via an unspecified route of administration on 13Jul2021 (Batch/Lot Number: EW0178) as SINGLE for covid-19 immunization. The patient denied for any medical history and concomitant medications. It was reported that the patient took her 1st dose in Jul2021, maybe the second week of Jul2021 and had a little shoulder soreness that day and it had only lasted a couple of days. She didn't even see a mark barely where shoulder the COVID vaccine. The patient confirms that she recovered completely from this. The outcome of event was recovered in Jul2021. 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: 1673155
Sex: M
Age:
State:

Vax Date: 07/01/2021
Onset Date: 07/01/2021
Rec V Date: 09/04/2021
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: 202107; Test Name: body temperature; Result Unstructured Data: Test Result:100; Comments: got a low grade fever like 100, 99, 100; Test Date: 202107; Test Name: body temperature; Result Unstructured Data: Test Result:99; Comments: got a low grade fever like 100, 99, 100; Test Date: 202107; Test Name: body temperature; Result Unstructured Data: Test Result:100; Comments: got a low grade fever like 100, 99, 100

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: he is real sick; He is weak; Low grade fever like 100, 99, 100; had 'back' pain; he is kind of not feeling good; This is a spontaneous report from a contactable consumer. A male patient of unspecified age and gender received Pfizer Covid 19 (BNT162B2) (Batch/Lot number: Unknown, Expiration date: Unknown), on an unspecified date in Jul2021 as Dose 1 single for covid 19 immunization.The patient had not received any other vaccine and other medication in two weeks. The patient had not affected with covid19 before or after vaccination. Medical history and Concomitant medications were not reported. On an unspecified date 9 days ago (Jul2021) after they both got the Pfizer Covid shot and reporter did not had any side effect but her husband was real sick and he got sick the next day he came out the bed. He was weak and had got a low grade fever like 100, 99, 100 also he had back pain and had not got better and was kind of not feeling good. Reporter stated that she just want to know if that was one of the symptom and she also had went to the symptoms but it did not say anything about the back pain. It was reported that when they told about the role of Pfizer drug safety and Medical information department, she said that she did not understand and told them to forgot about it. No known Allergies were reported. On an unknown date in Jul2021 patient underwent lab tests and procedures which included body temperature (100,99,100). No therapeutic treatments were received. The outcome of the events were reported as unknown and back pain was reported as Not recovered/Not resolved. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1673156
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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: Had unbelievable arthritis pain/ my flare; Hands and fingers were swollen; Had unbelievable arthritis pain/pain woke the patient up at night; This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received of BNT162B2 (PFIZER-BIONTECH COVID-19 Vaccine, solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date at an dose number unknown, single for COVID-19 immunization. The patient's medical history was not reported. The concomitant medications were not reported. The patient previously took Xeljanz (XELJANZ) and experienced lack of efficacy and arthritis pain. The patient stated that she spoke with safety department yesterday. The patient has been taking Xeljanz for years. The patient retired recently and had to change her insurance. Starting 01Jul, the patient got 3 bottles of Xeljanz in the mail. After that first bottle and started the second bottle, it was like the patient was not taking any Xeljanz at all. The patient knew what that feels like because when she got the COVID vaccine, her doctor wanted her to pause Xeljanz and she had unbelievable arthritis pain. The patient's hands and fingers were swollen. The pain woke the patient up at night. The patient told her doctor about her flare and he told her double her prednisone dose. The outcome of events were unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1673157
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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: This is a spontaneous report from a contactable consumer or other non-hcp. A female patient of an unknown age received (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: unknown, expiration date: unknown), via an unspecified route, on an unknown date as DOSE NUMBER UNKNOWN, SINGLE for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The reporter mentioned that she looked online this morning when she was trying to do some research on her own and she saw that there was another lady arm that looked just like that. The caller had her son take a picture and the caller's arm looks just like the lady's arm that she saw online where the COVID vaccine went in. Reporter stated that this was just something that she saw when she was looking up her own side effects and searched swelling in arm and she was looking at someone's website, maybe USA Today, and they had a picture of the lady arm. The outcome of event is unknown. Follow-up attempts are completed. No further information is expected. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1673158
Sex: U
Age:
State:

Vax Date: 07/31/2021
Onset Date: 08/01/2021
Rec V Date: 09/04/2021
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: Pain in extremity

Symptoms: Chest pain; I have the AstraZeneca on July 24 the 1st shot and then I had Pfizer 2nd one; This is a spontaneous report from a contactable consumer (patient, self-reported). A 59-year-old patient of an unspecified gender received second dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EW0179 and expiry date was not reported), via an unspecified route of administration, on 31Jul2021 (age at vaccination: 59 years), as a single dose for COVID-19 immunization and first dose of COVID-19 VACCINE NRVV AD (CHADOX1 NCOV-19, lot number and expiry date were not reported), via an unspecified route of administration, on 24Jul2021, as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that on 01Aug2021, the patient experienced Chest pain and I have the AstraZeneca on 24lthe 1st shot and then I had Pfizer 2nd one on an unspecified date in 2021. The patient stated, "Well little bit concerned, I have the AstraZeneca (Further not clarified hence captured as Unspecified vaccine) on July 24 the 1st shot and then I had Pfizer 2nd one the Pfizer (Confirmed as Covid 19 vaccine) Yes, the Pfizer would be second one the 1st one is 24Jul AtraZeneca the second one was Pfizer I took it on July 31st on the Aug 1st, I had chest pain and I didn't go and see doctor today." The patient stated, "the reason I called is just wanna ask how bad would this chest pain going to be and how long would it it last normally the CDC has indicated it last may be 14 days." Further probing could not be done as the consumer was not willing to provide further information. Outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1673159
Sex: U
Age:
State:

Vax Date: 07/28/2021
Onset Date: 08/02/2021
Rec V Date: 09/04/2021
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: Rash started developing all over my body, on both of my forearms and all over my neck, started moving up to my face; Rash started developing all over my body, on both of my forearms and all over my neck, started moving up to my face; Rash started developing all over my body, on both of my forearms and all over my neck, started moving up to my face; Rash started developing all over my body, on both of my forearms and all over my neck, started moving up to my face; Have rash on my chest, it look like hives; Migraine; This is a spontaneous report from a contactable consumer (Patient). A patient of an unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on 28Jul2021 as single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. On 02Aug2021, the patient experienced Migraine. On 03Aug2021, the patient experienced Rash started developing all over my body, on both of my forearms and all over my neck, started moving up to my face and Have rash on my chest, it look like hives. It was reported that Consumer stated, I got my Pfizer Vaccine last week on Wednesday and on Monday I had a migraine and on Tuesday a rash all started developing all over my body now it's Thursday I have a rash on both of my forearms and rash all over my neck, started moving up to my face and I have rash on my chest, it look like hives my little Pink sheet from the(Clarification unknown) says to call this number to report any side effects but I am hoping if you could tell me what to take to counteract, so it can go away and how long the rash was normally being reported or how long it stays. Outcome of all the events was unknown. Information about the Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1673160
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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: Quite Skin rash; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19, Solution for injection, Batch/Lot Number: EW0179), 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, patient had a rash from the Covid shot (Vaccine) and also reported that I woke up with quite skin rash and stated I know that, It was a side effect and enquired as "Can I take Benadryl or Benadryl cream on the rash?" The patient stated I want to know, Can I take a Benadryl. You know the Benadryl has been anti-histamine to help with itching rash and can I take Over the Counter Benadryl?". The outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1673161
Sex: F
Age:
State: NY

Vax Date: 07/01/2021
Onset Date: 07/05/2021
Rec V Date: 09/04/2021
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: Thyroiditis sabacute; I had a menstrual period that lasted for over 2 weeks; This is a spontaneous report from contactable other health professional (patient). A 27-year-old non pregnant female patient reported for herself that she received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch number/Lot number: EW0177), via an unspecified route of administration, administered in left arm on 01Jul2021 at 04:45 PM (age at vaccination was 27 years) as dose 1, single for COVID-19 immunisation. The patient was not pregnant at the time of vaccination. Vaccination facility was pharmacy or drug store. Medical history and concomitant medications were not reported. No known allergies reported. The patient did not receive other vaccine in four weeks and did not receive other medications in two weeks. After getting the first vaccination, on 05Jul2021 at 08:00 AM, the patient experienced subacute thyroiditis, as per Endocrinologist and also had a menstrual period that lasted for over 2 weeks, despite having a normal cycle the week prior to taking the vaccine. Adverse events resulted in doctor or other healthcare professional office/clinic visit. The patient did not receive treatment for adverse events. No covid prior vaccination and not tested covid post vaccination. Outcome of the events was recovered/resolved with sequel.

Other Meds:

Current Illness:

ID: 1673162
Sex: F
Age:
State: NY

Vax Date: 04/19/2021
Onset Date: 07/01/2021
Rec V Date: 09/04/2021
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: She began to have the memory issues and are progressively getting worse; And I cannot think ,I do not want to think; She began to have the memory issues and are progressively getting worse; I have a problem with my attention, cannot pay attention; This is a spontaneous report received from Pfizer sponsored program Support from a contactable consumer (patient). A female patient of an unspecified age received bnt162b2 (BIONTECH COVID-19 VACCINE, solution for injection, Lot number was not reported, NDC number was not reported) dose 2 via an unspecified route of administration on 19Apr2021 as dose 2, single for COVID-19 immunisation. The patient medical history and concomitant medication was not reported. Historical vaccine included BNT162B2 dose 1 on an unspecified date for COVID-19 immunisation. No other product was given. No investigation assessment was reported. On Jul2021 the patient experienced she began to have the memory issues and are progressively getting worse, and I cannot think, I do not want to think, I have a problem with my attention, cannot pay attention. No PQC was present. The Patient stated that after the second dose, for the last 4 weeks, she had been having memory issues and attention issues. She can't not think and does not want to think but she has lots to do. On her own she did a study where she spoke to 2 friends who are having similar issues. One was a friend and the other was a young healthcare provider. They reported memory issues but not attention problems. These are things she was ashamed of, that she cannot remember what she was supposed to do or not do. She wants us to know there are more side effects other than physical ones. She wanted Pfizer to know that there are other things going on. She never had memory issue until the vaccine. The caller disconnected prior to the conference of the call: Agent explains the caller was reluctant to provide any information on herself for the report, she declined her last name and address. The clinical outcome of the events was unknown. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1673163
Sex: F
Age:
State:

Vax Date: 08/05/2021
Onset Date: 08/06/2021
Rec V Date: 09/04/2021
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: 20210806; Test Name: fever; Result Unstructured Data: Test Result:99 Fahrenheit; Comments: I am running like a 99 fever

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: chills; I am running like a 99 fever; headache; I don't feel good; This is a spontaneous report from a contactable consumer, the patient. A 62-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, lot number: EW0198), via an unspecified route of administration on 05Aug2021 as dose 1, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. On 06Aug2021, the patient experienced chills, running like a 99 fever, headache and did not feel good. The reporter stated that she did not feel good hence she go on and took something to get rid of her headache that could lower her fever so she would feel better. The outcome of the events was not recovered.

Other Meds:

Current Illness:

ID: 1673164
Sex: F
Age:
State: GA

Vax Date: 07/28/2021
Onset Date: 07/29/2021
Rec V Date: 09/04/2021
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: antibody test; Result Unstructured Data: Test Result:none; Comments: I had antibodies going into the vaccine semi quantitative Covid antibody titer score of 18 going into shot 1.; Test Date: 20200727; Test Name: PCR test; Test Result: Positive

Allergies:

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

Symptoms: Sore arm; fatigued; foggy; Off balance; Diarrhea; Short of breath; chest tightness; dysautonomia; Low BP readings to high BP readings; Feel crummy; High heart rate days 7 onward post vaccine.; High blood pressure; This is a spontaneous report from a contactable consumer or other non hcp. A 54-years-old non pregnant female patient received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/lot number: Not Known, Expiration Date: not reported), dose 1 via an unspecified route of administration, administered in Arm Right on (Age at vaccination 54 Years) 28Jul2021 11:45 as DOSE 1, SINGLE for covid-19 immunisation. Medical history included blood pressure increased, covid-19 from 27Jul2020 to an unknown date recovered. Concomitant medication(s) included telmisartan (TELMISARTAN) taken for blood pressure measurement. Prior to vaccination, patient diagnosed with COVID-19. Since the vaccination, patient was not been tested for COVID-19. The patient was not received any other vaccines within 4 weeks prior to the COVID vaccin. The patient received other medications within 2 weeks of vaccination is Blood pressure med telemesartan. Clinical course follows as 19 days post vaccine symptoms. I have long covid and this flared my long covid. First three days were textbook symptoms. Sore arm, fatigued, foggy. Then starting days 5 onward I literally went through long covid again. Blood pressure seriously went crazy day 8 onward past vax. Low BP readings to high BP readings. Bottom number the systolic moved up 10-18 points for 10 days. Heart rate increased. About 15 points for 2 weeks. And I'm on blood pressure medication!!!! Felt dysautonomia return. Off balance post shot 1 for a week. Diarrhea for a few days. Short of breath returned for 2 days. Then chest tightness returned for 4 days. Still have a little. No this was not psychological. This was real. Very real. Start of day 19 post vaccine I'm starting to feel a bit more like Pre vaccine baseline. On 29Jul2021 12:00, The patient experienced high heart rate days 7 onward post vaccine, high blood pressure, On Aug2021, feel crummy and low bp readings to high bp readings, dysautonomia, On 01Aug2021, sore arm, fatigued, foggy, off balance, diarrhea, short of breath, chest tightness. The patient underwent lab tests and procedures which included antibody test: none on I had antibodies going into the vaccine with a lab Corp semi quantitative Covid antibody titer score of 18 going into shot 1, sars-cov-2 test: positive on 27Jul2020. No treatment was received. AE resulted in Doctor or other healthcare professional office/clinic visit. The outcome of the events high heart rate days 7 onward post vaccine, high blood pressure, feel crummy was not recovered and remaining events are recovering. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up

Other Meds: TELMISARTAN

Current Illness:

ID: 1673165
Sex: F
Age:
State: WA

Vax Date: 07/10/2021
Onset Date: 08/03/2021
Rec V Date: 09/04/2021
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: Ear infection; This is a spontaneous report from a contactable consumer, the patient. A 39-year-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration on 10Jul2021 at 10:00 (at the age of 39-year-old) as a single dose for COVID-19 immunisation. The patient had no medical history and had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any concomitant medications within two weeks of vaccination. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient previously took the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration on an unknown date as a single dose for COVID-19 immunisation. On 03Aug2021 the patient experienced an ear infection. The event did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. It was unknown whether any therapeutic measures were taken as a result of the event. Since the vaccination, the patient had not been tested for COVID-19. The clinical outcome of the event ear infection was not recovered at the time of this report. The lot number for BNT162b2 was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1673166
Sex: M
Age:
State:

Vax Date: 08/05/2021
Onset Date: 08/01/2021
Rec V Date: 09/04/2021
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: Chest aches; Legs and whole body hurts; Legs and whole body hurts; Left ear hurts; Not feeling well; This is a spontaneous report from a contactable consumer. This consumer (patient's wife) reported for a male patient (reporter's husband). A male patient of unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, batch/lot number unknown) via an unspecified route of administration on 05Aug2021 as DOSE 2, SINGLE for COVID-19 Immunisation. The patient's medical history and concomitant medications were not reported. He previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, batch/lot number unknown) via an unspecified route of administration on unspecified date as DOSE 1, SINGLE for COVID-19 Immunisation. The patient was not feeling well, chest aches, legs and whole body hurts and left ear hurts. Reporter agreed that she will contact her husband's healthcare provider and she stated that patient got the second vaccine on the previous day of reporting. The outcome of events was unknown. The lot number for the vaccine, [BNT162B2], was not provided and requested during follow up.

Other Meds:

Current Illness:

ID: 1673167
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/04/2021
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 arm that I got my shot, in my arm, it just keep shaking; This is a spontaneous report from a contactable consumer (patient). A patient of an unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as DOSE NUMBER UNKNOWN, SINGLE for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced the arm that I got my shot, in my arm, it just keep shaking. The patient was having side effects from the shot so, where the arm that the patient got shot started really shaking; The patient got shot, in arm, it just kept shaking. The clinical outcome for the event was unknown. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am