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: 1718441
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/21/2021
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: itchiness; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on an unspecified date (Lot number was not reported) as dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced nonstop itchiness in her hand post vaccination on an unspecified date. 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: 1718442
Sex: M
Age:
State: TX

Vax Date: 03/07/2021
Onset Date: 03/08/2021
Rec V Date: 09/21/2021
Hospital:

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

Lab Data: Test Name: blood pressure; Result Unstructured Data: Test Result:High; Test Name: testosterone; Result Unstructured Data: Test Result: low.

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: nausea; fever; chills; diarrhea; This is a spontaneous report from a contactable consumer (patient). A 46-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in right arm on 07Mar2021 17:30 (Batch/Lot number was not reported) as dose 1, single for COVID-19 immunisation. Medical history included high blood pressure, low testosterone, and thyroid. Patient had no known allergies and was not diagnosed with COVID prior to vaccination. The patient's concomitant medications were not reported. Patient had no other vaccine in four weeks. On 08Mar2021, the patient experienced nausea, fever, chills and diarrhea. No treatment was received for the events. Outcome of the events was not recovered. Patient had not been tested for COVID post vaccination. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718443
Sex: M
Age:
State: NY

Vax Date: 03/07/2021
Onset Date: 03/07/2021
Rec V Date: 09/21/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Severe nasal congestion; sneezing; This is a spontaneous report from a contactable consumer (patient). A 63-year-old male patient received BNT162B2(PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot Number: En 6205), via an unspecified route of administration, administered in right arm on 07Mar2021 09:30 (at the age of 63-years-old) as dose 1, single for covid-19 immunization. Medical history included hypertension. Patient had concomitant medication. The patient experienced severe nasal congestion and sneezing on 07Mar2021 18:00. No treatment was taken for the events. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1718444
Sex: F
Age:
State: ID

Vax Date: 03/07/2021
Onset Date: 03/08/2021
Rec V Date: 09/21/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: Body aches; Fatigue; Headache; Low grade fever; This is a spontaneous report from a contactable consumer (patient). A 45-year-old female patient received BNT162B2 (Pfizer-BioNTech COVID-19 vaccine), via an unspecified route of administration, administered in the right arm on 07Mar2021 at 08:45 (Lot Number: En6204) as dose 2, single for COVID-19 immunization. The patient medical history was not reported. The patient had no known allergies and did not have COVID-19 prior to vaccination. Concomitant medication includes unspecified birth control. The patient was not tested for COVID post vaccination. The patient previously received the first dose of BNT162B2 on an unknown date for COVID-19 immunization. The patient experienced body aches, fatigue, headache and low grade fever on 08Mar2021 at 03:00. The patient did not receive treatment for the events. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1718445
Sex: F
Age:
State:

Vax Date: 02/25/2021
Onset Date: 02/26/2021
Rec V Date: 09/21/2021
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: 20210226; Test Name: temperature; Result Unstructured Data: Test Result:100-101.9 Fahrenheit; Test Date: 20210227; Test Name: temperature; Result Unstructured Data: Test Result:99 Fahrenheit

Allergies:

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

Symptoms: tired; shivering; Extremely itchy/ Still very itchy; large red area where the shot was given/ red, but less red than days before.; temperature was 100F-101.9F; This is a spontaneous report from a non-contactable consumer (patient). A 95-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EL9262), via an unspecified route of administration on 25Feb2021 (at the age of 95-years-old) as dose number unknown, single for COVID-19 immunization. Medical history included transient ischaemic attack which started 16 months ago. The patient had no known allergies. The patient's concomitant medications were not reported. The patient was not pregnant at the time of vaccination. No other vaccine was given in four weeks. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination has not been tested for COVID-19. The patient was extremely itchy and had a large red area where the shot was given on 26Feb2021. The patient was still very itchy, red, but less red than days before at the time of report. The patient temperature was 100F-101.9F on 26Feb2021 19:30. The patient called 911 and took acetaminophen, liquids, cool compress, get rid of electric blanket, and used wool and/or cotton blankets as treatment. The patient was shivering like she was all day on 26Feb2021. On 27Feb2021, morning, the temperature was 99 F, felt better and was very tired. On 28Feb2021 patient requested going out for a joyride. The outcome of event pyrexia was recovered on an unspecified date. The outcome of all other events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1718446
Sex: F
Age:
State: CA

Vax Date: 01/21/2021
Onset Date: 02/10/2021
Rec V Date: 09/21/2021
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: Test Date: 20210302; Test Name: nasal Swab; Test Result: Negative

Allergies:

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

Symptoms: Rash; This is a spontaneous report from a contactable nurse (patient). A 55-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration, administered in arm left on 21Jan2021 15:00 (Batch/Lot Number: EL9261) (at age 55-years old) as dose 2, single for covid-19 immunisation. The first dose was received on 31Dec2020 (lot number: EL0142) (at age 55-years-old) on the left arm. Medical history included known allergies. The patient's concomitant medications were not reported. There were no other vaccines within four weeks. The patient experienced rash that showed up on L side of face & neck & then sporadically over body on 10Feb2021 15:00. Rash continues to show up as of 08Mar2021 date. Treatment was given for the event that resulted in ER visit and physician's office visit. Outcome of the event was not recovered. Patient was not diagnosed with covid previously and had been tested post vaccination on 02Mar2021: nasal swab: negative. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1718447
Sex: F
Age:
State:

Vax Date:
Onset Date: 03/05/2021
Rec V Date: 09/21/2021
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: Diarrhea; Nausea; Dizziness; Fever; Chills; Aches; This is a spontaneous report from a non-contactable consumer (patient). A 23-years-old non-pregnant female patient received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number and Expiration date was not reported), 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. Patient had no other vaccine in four weeks. Patient was not diagnosed with COVID-19, prior to vaccination and unknown if patient had been tested for the COVID-19, post vaccination. On 05Mar2021 at 19:00 hours, patient experienced diarrhea, nausea, dizziness, fever, chills and aches. Patient received no treatment for the events. The outcome of all the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot been obtained

Other Meds:

Current Illness:

ID: 1718448
Sex: F
Age:
State: FL

Vax Date: 03/04/2021
Onset Date: 03/01/2021
Rec V Date: 09/21/2021
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: felt unusual; tiredness; soreness of the arm and hip; soreness of the arm and hip; This is a spontaneous report from a contactable consumer (patient herself) via Pfizer-sponsored program. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on 04Mar2021 as Dose 1, single for Covid-19 immunization. The patient's medical history included asthma (she had asthma but did not feel shortness of breath). The patient's concomitant medications were not reported. She received her first dose yesterday. According to her, she has asthma but did not feel shortness of breath. However, she felt unusual, nothing severe. She felt tiredness, soreness of the arm and hip after the 1st dose. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718449
Sex: F
Age:
State: TX

Vax Date: 03/02/2021
Onset Date:
Rec V Date: 09/21/2021
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: Rash on the right side where I had the Pfizer vaccination, rash on both arms; Seem like it has fever in because that area is warm, to the touch is warm and a little sore; Pain towards my ear, to my head; pain in my left ear and head; Itching; Headache; Swelling like almost that part of the arm where the injection site is; still was a little redness; where the injection site is, still was a little redness and still a little sore; This is a spontaneous report from a contactable consumer (Patient). A 82-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 on 02Mar2021(at the age of 82-years-old) as a single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced Rash on the right side where I had the Pfizer vaccination, rash on both arms , Seem like it has fever in because that area is warm, to the touch is warm and a little sore, Pain towards my ear, to my head; pain in my left ear and head, When I lean down I got like pump bump, but when I raise up it wouldn't be there it wasn't a continuous thing, Itching , Headache, Swelling like almost that part of the arm where the injection site is, still was a little redness and still a little sore. Consumer stated, It look like EN and then it look like X2O3, that's what it looks like I am not sure about that, I think it's ENX2O3. It might not be that, it might be 62O3, it might be that. All I know that last number is 62O3, it's EN something. Consumer stated, With the Itching I still have the little rashes on my arm and my arm is still a little sore, not as sore as it was yesterday but still a little sore with my head when I stoop down is not as bad. The event was not worsened. Patient did not take anything for that because that happened during the night while she was asleep. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1718450
Sex: F
Age:
State: CA

Vax Date: 02/26/2021
Onset Date: 02/26/2021
Rec V Date: 09/21/2021
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: inflammation of hands and feet after 48 hours such that I couldnot get one shoe on; body aches from hours 12-48; sweats without fever from hours 8-48; chills at 6 hours; headache within 15 minutes; overall malaise; intestinal issues (gas, cramps, diarrhea then constipation); as if my system has been in shock; intestinal issues (gas, cramps, diarrhea then constipation); intestinal issues (gas, cramps, diarrhea then constipation); intestinal issues (gas, cramps, diarrhea then constipation); excessive sleepiness for last 10 days; This is a spontaneous report from a non-contactable consumer (patient). A 60-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EN6198), via an unspecified route of administration, administered in Left arm on 26Feb2021 09:00 (at the age of 60 year old) as dose 1, single for COVID-19 immunisation. Medical history included mitral valve prolapse, osteoarthritis, skin cancer from an unknown date. Patient has known allergies to penicillin and erythromycin. Concomitant medications included cetirizine hydrochloride (ZYRTEC ALLERGY) taken for an unspecified indication. Prior vaccination, patient was not diagnosed with COVID-19 and did not receive other vaccine in four weeks. Patient was not pregnant at the time of vaccination. On 26Feb2021, within 15 minutes, patient experienced headache, chills at 6 hours, sweats without fever from hours 8-48, body aches from hours 12-48, intestinal issues (gas, cramps, diarrhea then constipation), excessive sleepiness for last 10 days, and overall malaise, as if her system has been in shock.. After 48 hours, on 28Feb2021, patient had inflammation of hands and feet, so she removed rings and could not get one shoe on. Since the vaccination, patient had not been tested for COVID. No treatment was received in response to the events. The outcome of the events was recovered with lasting effects. No follow-up attempts are possible. No further information is expected.

Other Meds: ZYRTEC ALLERGY.

Current Illness:

ID: 1718451
Sex: F
Age:
State: TX

Vax Date: 01/30/2021
Onset Date:
Rec V Date: 09/21/2021
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: lymph nodes swollen under her neck, arm pits, and the back of arms; problems breathing; a lot of headaches; tenderness around the shot site; A lot of joint pains especially in the hips; The first one from January has not healed. It makes a scab and it comes off. It is not healing.; This is a spontaneous report from a contactable consumer (patient). A 71-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection, lot number: EN5318, expiration date not reported) via an unspecified route of administration, in left arm, on 30Jan2021 16:00 (at the age of 71-years-old), at dose 1, single for covid-19 immunization from convention center. Medical history included asthma, arthritis, diabetes, cholesterol, reflux (as reported), allergies, vitamin d (as reported). Concomitant medications included glipizide for diabetes; liraglutide (VICTOZA); lisinopril taken for diabetes to keep her kidneys healthy; rosuvastatin calcium (ROSUVASTIN) taken for cholesterol; fenofibric acid taken for reflux; montelukast sodium (MONTELUKAST) taken for allergy; cyanocobalamin (VITAMIN B12) taken for vitamin d; meloxicam taken for arthritis, mometasone furoate (NASONEX); ergocalciferol (VITAMIN D) taken for unspecific indication. Historical vaccine included flu shot (FLU) administered on 11Sep2020 (Fluad quad 2020 2021 syringe. HARX: 120345300 (as reported), lot number, expiry date: unknown) from pharmacy. No additional vaccines administered on the same date of vaccination. On an unspecified date after vaccination in 2021, the patient experienced lymph nodes swollen under her neck, arm pits, and the back of arms, a lot of headaches, a lot of joint pains especially in the hips, tenderness around the shot site and the vaccination site has not healed. It made a scab and came off. After 2 to 2.5 hours of vaccination, the patient also had problems of breathing. The patient had her second dose of vaccination on 05Mar2021 for COVID-19 immunization. The patient had no investigation assessments. Therapeutic measures were taken for problems breathing included nebulizer and albuterol emergency inhaler. The outcome of the event vaccination site has not healed/ a scab was not recovered and outcome of other events was unknown. No follow up attempts are possible. No further information is expected.

Other Meds: GLIPIZIDE; VICTOZA; LISINOPRIL; ROSUVASTIN; FENOFIBRIC ACID; MONTELUKAST [MONTELUKAST SODIUM]; VITAMIN B12 [CYANOCOBALAMIN]; NASONEX; VITAMIN D [ERGOCALCIFEROL]; MELOXICAM.

Current Illness:

ID: 1718452
Sex: F
Age:
State: TX

Vax Date: 02/03/2021
Onset Date: 02/04/2021
Rec V Date: 09/21/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: she woke up and couldn't taste anything; This is a spontaneous report from a contactable consumer (patient). A 76-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Lot number: EL9265, Expiration date was not reported), via an unspecified route of administration (administered on the left arm) on 03Feb2021 at 10:30 (at the age of 75-years-old) as dose 1, single for COVID-19 immunisation. Medical history included blood pressure, diabetes type II, restless legs, fibromyalgia, and anticoagulant therapy all from an unknown date. Concomitant medications included pantoprazole, atorvastatin, pramipexole taken for restless legs, acetylsalicylic acid (BAYER ASPIRIN), clopidogrel taken for blood thinner, gabapentin taken for fibromyalgia, fluoxetine, valsartan taken for blood pressure, metformin taken for diabetes, ubidecarenone (COQ-10), fish oil, vitamin d3, and ascorbic acid (VITAMIN C); start and stop date were not reported. On 04Feb2021 between 5:00 AM and 6:00AM, the patient noticed she couldn't taste anything. The patient further reported that she lost her sense of taste. The patient then received second dose of BNT162B2 on 23Feb2021 and stated that she still does not have her sense of taste. The patient wanted to know when she will get her taste back and how long will this last. After her second dose, the patient went to the doctor for UT infection and asked the doctor about not being able to taste. The patient has not recovered from the event. No follow-up attempts are possible. No further information expected.

Other Meds: PANTOPRAZOLE; ATORVASTATIN; PRAMIPEXOLE; BAYER ASPIRIN; CLOPIDOGREL; GABAPENTIN; FLUOXETINE; VALSARTAN; METFORMIN; COQ-10; FISH OIL; VITAMIN D3; VITAMIN C [ASCORBIC ACID]

Current Illness:

ID: 1718453
Sex: M
Age:
State: NJ

Vax Date: 03/03/2021
Onset Date:
Rec V Date: 09/21/2021
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: felt like he was getting a rash on stomach on chest; This is a spontaneous report from a contactable consumer (patient) via Regulatory Authority. A male patient of an unspecified age received the first dose of BNT162B2 (Pfizer-BIONTECH COVID-19 Vaccine), via an unspecified route of administration on 03Mar2021 (Batch/Lot number was not reported) single, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient felt like he was getting a rash on stomach on chest on an unspecified date. He stated that he hasn't gotten worse but hasn't gotten better either and was inquiring if he should get his second dose on 24Mar2021. Outcome of the events was not recovered. No follow-up attempts are possible; information about the lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718454
Sex: F
Age:
State: PA

Vax Date:
Onset Date:
Rec V Date: 09/21/2021
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: red rash all over the body; This is a spontaneous report from a contactable consumer reporting on behalf of the patient via a Pfizer-sponsored program. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), 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. It was reported that the patient received the vaccine on Saturday (unspecified date). The patient experienced red rash all over the body on unspecified date. The reporter asked if the patient should go to the hospital. Outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718455
Sex: M
Age:
State: MA

Vax Date: 02/18/2021
Onset Date: 02/18/2021
Rec V Date: 09/21/2021
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: Rash. Started under armpit and has spread over body. It is spotted and not a continuous rash. I thought it resembled psoriasis spots; Administration date= 04Feb2021/Other vaccine same date vaccine date=18Feb2021; This is a spontaneous report from a contactable consumer (patient). A 44-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number was not reported), via an unspecified route of administration, administered in Arm Left on 18Feb2021 as dose 2, single for covid-19 immunisation from workplace clinic. Medical history included hashimoto's and no known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with covid prior to vaccination and patient was not tested for COVID-19 post vaccination. On 25Feb2021, patient experienced rash started under armpit and has spread over body. it is spotted and not a continuous rash. Patient thought it resembled psoriasis spots and never had anything like it until vaccination. Patient see the doctor next week. The patient administration date dose on 04feb2021 and other vaccine same date vaccine date on 18Feb2021. The outcome of event rash was not recovered.

Other Meds:

Current Illness:

ID: 1718456
Sex: F
Age:
State: IL

Vax Date: 03/03/2021
Onset Date: 03/04/2021
Rec V Date: 09/21/2021
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: just been feeling off; headache; tightness in lungs; loose stool; This is a spontaneous report from a contactable health care professional (patient). A 47-year-old non-pregnant female patient received BNT162B2 (Pfizer-BioNTech COVID-19 vaccine), via an unspecified route of administration, administered in the right arm on 03Mar2021 at 15:00 (Lot Number: EN6202) as dose 1, single for COVID-19 immunization. Medical history Hashimotos, Polyarthritis (most likely psoriatic) and allergies to sulfa antibiotics, penicillin (reported as PCN), scallops and gluten all from unknown dates. The patient did not have COVID prior to vaccination. The patient was not tested for COVID post vaccination. Concomitant medications included levothyroxine sodium (SYNTHROID); liothyronine sodium (CYTOMEL); trazodone (manufacturer unknown); etanercept (ENBREL) and semaglutide (OZEMPIC), all taken for an unspecified indication, start and stop date were not reported. The patient experienced headache, tightness in lungs, loose stool and has just been feeling off on 04Mar2021 at 07:15. The patient did not receive treatment for the events. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: SYNTHROID; CYTOMEL; TRAZODONE; ENBREL; OZEMPIC

Current Illness:

ID: 1718457
Sex: M
Age:
State: TN

Vax Date: 03/05/2021
Onset Date:
Rec V Date: 09/21/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: blisters; fever; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (spouse) reported that a male patient of an unspecified age received bnt162b2 (Pfizer Covid-19 Vaccine), dose 1 via an unspecified route of administration on 05Mar2021 (Lot number was not reported) as dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On unspecified date in 2021, the patient developed blisters and fever after having his first dose. He took Valacyclovir for the events. His next supposed dose will be on 26Mar2021. 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: 1718458
Sex: F
Age:
State:

Vax Date: 02/22/2021
Onset Date:
Rec V Date: 09/21/2021
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: rash from head to toe; This is a spontaneous report. A non-contactable other healthcare professional reported that a female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number was not reported, Expiration Date: 22Feb2021), via an unspecified route of administration on 22Feb2021 as dose 1, single for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced rash from head to toe with outcome of unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718459
Sex: F
Age:
State: MD

Vax Date:
Onset Date:
Rec V Date: 09/21/2021
Hospital:

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

Lab Data: Test Date: 03/07/2021; Test Name: COVID test; Result Unstructured Data: Test Result:unknown results

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: This is a spontaneous report from a contactable nurse (patient). A 59-year-old female patient received the 1st dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine; batch/lot# EN6208), at the age of 59, via an unspecified route of administration, on an unspecified date, single dose, for COVID-19 immunisation. The patient had no medical history and there were no concomitant medications. The patient stated that she took the COVID-19 vaccine on Monday. She had been sick since that Monday until the day of report. The patient stated the symptoms they go and come back and same again. On Monday, patient's arm was sore (that was expected). On Tuesday morning she woke up with a cough. On Wednesday, she had fever, and had been shivering. The patient had fever and a cough. On Thursday, the cough stopped, and she had diarrhea. On Friday, patient had a headache and lost her taste. She lost taste since that Friday until the day of report. The patient was coughing and shivering no matter what she took. Nothing really helped. The patient took Tylenol. It helped for a while, then after that she went back to the same point again. The patient stated the cough was back where it was before. The patient could not even go to work, she felt so weak. She had muscle aches all over her body; her bone all over. She was wondering if she had to go for the second dose. The patient underwent lab tests and procedures, which included COVID test: result unknown on Mar 7, 2021. The outcome of cough, shivering, lost taste: not recovered; and outcome of other events: unknown. No follow-up attempts possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718460
Sex: M
Age:
State: NC

Vax Date: 03/06/2021
Onset Date: 03/07/2021
Rec V Date: 09/21/2021
Hospital:

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

Lab Data: Test Name: blood work; Result Unstructured Data: Test Result:unknown results; Comments: received a lab report but caller is unable to provide results

Allergies:

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

Symptoms: Dizziness; left arm was numb; fingers moved by themselves; felt like his tongue was swollen; lips were numb; slight headache; This is a spontaneous report from a contactable consumer (patient's wife). A 76-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration, administered in left arm on 06Mar2021 13:00 (Lot Number: EN6206) (a the age of 76-years-old) as dose 1, single for covid-19 immunisation. Medical history included ongoing diabetes and when his sugar dropped, he got dizzy and weak. Concomitant medications included metformin; rivaroxaban (XARELTO); metoprolol succinate; simvastatin; borago officinalis oil, fish oil, linum usitatissimum oil (TRIPLE OMEGA 3 6 9); cyanocobalamin (VITAMIN B12); colecalciferol (VITAMIN D3); all taken for an unspecified indication from an unspecified start date and ongoing. The patient did not have any prior vaccinations within 4 weeks. The patient was fine on 06Mar2021, day of vaccination. Towards the morning on 07Mar2021, he was feeling a little dizzy. His left arm was numb, and his fingers moved by themselves, his tongue felt like it was swollen, his lips were numb. He also had a slight headache. He slept until 4:30pm and took a nap for 5 hours. The reporter gave him a Tylenol as treatment. When the patient started seeing the doctor, he took blood work. He received a lab report, but reporter was unable to provide results. The event did not require emergency room visit but required physician office visit. The reporter was unsure if these are side effects. The outcome of dizziness, twitching and headache was unknown, and outcome of all other events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: METFORMIN; XARELTO; METOPROLOL SUCCINATE; SIMVASTATIN; TRIPLE OMEGA 3 6 9; VITAMIN B12 [CYANOCOBALAMIN]; VITAMIN D3

Current Illness: Diabetes

ID: 1718461
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/21/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: shoulder got very sore; the arm that they gave the shot in, my shoulder got very sore; This is a spontaneous report from a contactable consumer (patient). A 73-year-old patient of an unspecified gender received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as dose 1, single for COVID-19 immunisation. Medical history included 'arthritis in my shoulder.' The patient's concomitant medications were not reported. The patient was not reporting a severe reaction. Patient sated that "I have arthritis in my shoulder, the arm that they gave the shot in, my shoulder got very sore" on an unspecified date. The patient wanted to know if it was okay to take something for it like Acetaminophen or something. Somebody told the patient that Ibuprofen or Aspirin should not be taken. Patient did not know how many days it was not supposed to be taken for. Patient wanted to know if something could be taken for it or not. The patient still wanted to get the second shot. Outcome of the events was unknown. No follow-up attempts are possible. Information about Lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718462
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 09/21/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: body sweats; muscle pain; vomiting; fever; This is a spontaneous report from a Regulatory Authority. A contactable consumer (patient) reported that a 70-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) at the age of 70 years, as dose number unknown, single for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. Patient stated that she was currently out of Genotropin medication. She also stated that on an unspecified date, she was not feeling well post COVID vaccination as she has had body sweats, muscle pain, vomiting and a fever and she was not able to get out of the bed. Outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained

Other Meds:

Current Illness:

ID: 1718463
Sex: F
Age:
State: CT

Vax Date: 03/16/2021
Onset Date: 03/16/2021
Rec V Date: 09/21/2021
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: had tingling in my ring and pinky fingers that felt like it was falling asleep; dizziness; elevated heart rate/heart pounding; elevated heart rate/heart pounding; This is a spontaneous report from a contactable consumer or other non hcp (patient herself). A 40-years-old non pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Lot Number: EP 6955), (at the age of 40- years-old) via an unspecified route of administration, administered in Arm Right on 16Mar2021 13:45 as dose 1, single for COVID-19 immunisation. Medical history was none. Concomitant medications included ofloxacin (OFLOXACIN) taken for an unspecified indication, start and stop date were not reported. It was reported that she was not a pregnant at the time of vaccination. She was not diagnosed with COVID prior vaccination and not tested with COVID post vaccination. Patient had no known allergies. About 10 min after receipt of vaccine in right arm (16Mar2021 14:00), she had tingling in her ring and pinky fingers that felt like it was falling asleep. That was followed by dizziness and elevated heart rate/heart pounding. she had tinging. In her lips on the right side and her tongue. There was a funny taste in her mouth as well. She sat for a while but her heart was still pounding so requested to lay down. The tingling in her arm was not fully subsided 2 hours later and on 23Mar2021 seven days following first dose, the tingling recurred in the same area of her right arm, affecting the forearm and ring, pinky fingers. patient did not received treatment for adverse events. The outcome of events was recovering. No follow-up attempts are possible. No further information is expected

Other Meds: OFLOXACIN

Current Illness:

ID: 1718464
Sex: F
Age:
State: KY

Vax Date: 03/11/2021
Onset Date: 03/14/2021
Rec V Date: 09/21/2021
Hospital:

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

Lab Data: Test Date: 20210314; Test Name: Blood pressure; Result Unstructured Data: Test Result:Extremely high

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: woke up with nausea this morning, felt tired, her face broke out, was very red and her blood pressure was extremely high; woke up with nausea this morning, felt tired, her face broke out, was very red and her blood pressure was extremely high; woke up with nausea this morning, felt tired, her face broke out, was very red and her blood pressure was extremely high; woke up with nausea this morning, felt tired, her face broke out, was very red and her blood pressure was extremely high; woke up with nausea this morning, felt tired, her face broke out, was very red and her blood pressure was extremely high; This is a spontaneous report from a contactable consumer (patient) via a Pfizer sponsored Program. A female patient of an unspecified age received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number and Expiration date was not reported), via an unspecified route of administration on 11Mar2021 as dose 1, single for COVID-19 immunisation. The patient medical history included high blood pressure and concomitant medications included three unspecified medications for the high blood pressure. On 14Mar2021, patient woke up with nausea this morning, patient felt tired, her face broke out, was very red and her blood pressure was extremely high. It was never this high since she takes 3 medications for it. The outcome of all the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718465
Sex: F
Age:
State: OH

Vax Date: 02/19/2021
Onset Date: 02/19/2021
Rec V Date: 09/21/2021
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: she had bad allergies and was like a water faucet.; Felt really tired; This is a spontaneous report from a contactable consumer or other non-HCP (patient herself). A 51-year-old female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EN6200) via an unspecified route of administration in left arm on 19Feb2021 08:15 as dose 1, single (at the age of 51-years-old) for COVID-19 immunization. Patient medical history was not reported. The concomitant medications were reported as none. Family Medical History Relevant to adverse events included Nephew with Covid, Niece that had Covid. States she was not around them. She had a flu shot on an unspecified date in Oct2020 (reported as October) at, no issues voiced. Vaccination facility type was reported as School/Student Health Clinic. Patient did not receive the vaccine at a facility. On 19Feb2021, the patient felt really tired, starting around 13:00 to 14:00 the day of the vaccine. Felt done, tired, and went to bed early. Was tired from that Friday 19Feb2021 until that Sunday 21Feb2021. Felt better on Monday 22Feb2021. Patient stated that on 11Mar2021 she had bad allergies and was like a water faucet. She took children Benadryl 12.5mg 2 tablets and some eye drops. Stated that it helped. Thought she was allergic to something in the building. Patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- EN6204) via an unspecified route of administration in left arm on 12Mar2021 as dose 2, single for COVID-19 immunization. After receiving her second dose of the vaccine she thought she did not feel to bad at all, not tired like with the first one; until she woke up with this today. Patient experienced sore arm, Bells Palsy and she woke up her left eye felt weird after the second dose of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient mentioned she had no AEs prior to vaccination. Stated she was not the only one feeling tired, quite a few others were also. No further information or identifiers provided. The outcome of the event tiredness was resolved on 21Feb2021 while that of allergic reaction was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1718466
Sex: F
Age:
State: AZ

Vax Date:
Onset Date:
Rec V Date: 09/21/2021
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: Investigation; Result Unstructured Data: Test Result: lymph node in neck that was filled from infection; Comments: she has a lymph node in her neck that is filled, probably from infection

Allergies:

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

Symptoms: Diagnosed she has a lymph node in her neck that is filled, probably from infection; This is a spontaneous report from a non-contactable consumer (patient) via a REGULATORY authority. A female patient of unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/lot number: Unknown) via an unspecified route of administration, on an unknown date as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unknown date, the patient was diagnosed, she had a lymph node in her neck that was filled, probably from infection. The patient underwent lab tests and procedures which included investigation: resulted as she had a lymph node in her neck that was filled, probably from infection. Therapeutic measure was taken as a result of the event and patient was prescribed Amoxicillin for that. Inquiring if that would affect her Covid vaccine shot that she was scheduled to receive on Wednesday. The outcome of the event was unknown. No follow-up attempts are possible. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718467
Sex: M
Age:
State: LA

Vax Date:
Onset Date:
Rec V Date: 09/21/2021
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: was put on 2 medications for a sinus infection; This is a spontaneous report received from a sponsored program Support. A contactable consumer (patient) reported that: A male patient of an unspecified age received of first dose 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 as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unknown date, patient received 1st dose of Covid vacine and then was put on 2 medications for a sinus infection. The patient wondering if he can take medication and still take 2nd dose of Covid vaccine. Therapeutic measures were taken as a result of was put on 2 medications for a sinus infection (sinusitis). Outcome of event was reported as unknown. Information on the lot/batch number was requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1718468
Sex: M
Age:
State: WA

Vax Date:
Onset Date:
Rec V Date: 09/21/2021
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: Dizzy/Lightheaded; Stumbling; Vomiting; Headache; I have damage to my kidneys; Fever; This is a spontaneous report from a contactable consumer (patient). A 61-years-old male patient received unknown dose of bnt162b2 (BNT162B2, solution for injection), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as SINGLE for covid-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date, patient reported that his hands are a mess they're like a ball. Patient took Pfizer Vaccine and when he got up in the middle of the night he felt dizzy, stumbling and vomiting all night. Patient was vomiting with a headache for three days. He damaged his kidney and had lightheaded and fever. Patient was prescribed with Xeljanz 5 MG. The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718469
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/21/2021
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: Heart rate; Result Unstructured Data: Test Result:180-190; Test Name: HR; Result Unstructured Data: Test Result:HR in the 150s at times; Comments: HR in the 150s at times; Test Name: hx of svt; Result Unstructured Data: Test Result:Usually in high 200's or low 300's if it comes on; Comments: Usually in high 200's or low 300's if it comes on

Allergies:

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

Symptoms: During her 15 minute waiting period after the injection, the patient began to experience a change in her cough and felt nauseated; During her 15 minute waiting period after the injection, the patient began to experience a change in her cough and felt nauseated; She felt better shortly after 5 minutes but then her husband noted some redness in skin color in her legs and on her abdomen.; Upon arrival to bay, HR 180-190; This is a spontaneous report from a non-contactable other health care professional. A 70-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: ER8727), via an unspecified route of administration (at the age of 70-years), on 24Mar2021 as dose 2, single for COVID-19 immunization and received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: ER8727), via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. Medical history included dementia Alzheimer's type, Patient husband stated supraventricular tachy-cardia usually in high 200's or low 300's if it comes on, heart rate in the 150s at times from an unknown date and unknown if ongoing. The patient concomitant medications were not reported. On an unspecified date, the patient experienced during her 15 minute waiting period after the injection, the patient began to experience a change in her cough and felt nauseated, she felt better shortly after 5 minutes but then her husband noted some redness in skin color in her legs and on her abdomen, upon arrival to bay, hr 180-190. The treatment was received for the events with water and Trendelenburg position. The patient underwent lab tests and procedures which included heart rate increased: 180-190, heart rate increased: hr in the 150s at times HR in the 150s at times , supraventricular tachycardia: usually in high 200's or low 300's if it comes Usually in high 200's or low 300's if it comes on all on an unspecified date. Usually resolves on its own with elevation of feet above patient head per patient husband. Patient husband was main caregiver. He was not worried about it but wanted to know what her pressures were doing. Differential Diagnosis: Red flag symptoms. Follow up response to treatment: fair. Patient discharge. The clinical outcome of the events during her 15 minute waiting period after the injection, the patient began to experience a change in her cough and felt nauseated, she felt better shortly after 5 minutes but then her husband noted some redness in skin color in her legs and on her abdomen, upon arrival to bay, hr 180-190 was reported as unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1718470
Sex: F
Age:
State:

Vax Date: 03/26/2021
Onset Date: 03/26/2021
Rec V Date: 09/21/2021
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: Chills; fever; muscle aches; nausea; headache; This is a spontaneous report received from a contactable consumer or other non hcp. A 54-years-old non-pregnancy female patient received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/lot number was not reported) via an unspecified route of administration in Arm Left on 26Mar2021 at 15:00 (age at vaccination 54years old) as single dose for covid-19 immunisation. The patient was not pregnant at the time of vaccination. Medical history included hyperthyroidism from an unknown date and unknown if ongoing autoimmune disorders/allergies run in the family, drug hypersensitivity from an unknown date and unknown if ongoing, drug hypersensitivity from an unknown date and unknown if ongoing, drug hypersensitivity from an unknown date and unknown if ongoing , mycotic allergy from an unknown date and unknown if ongoing , food allergy from an unknown date and unknown if ongoing , food allergy from an unknown date and unknown if ongoing , dairy intolerance from an unknown date and unknown if ongoing. Prior to vaccination, the patient was diagnosed with COVID-19 reported as unknown. The patient did not receive any other vaccines within 4 weeks and other medications within 2 weeks prior to the COVID vaccine. The patient's concomitant medications were not reported. Since the vaccination, the patient had not been tested positive for COVID-19. On 26Mar2021 at 20:00 the patient experienced chills, fever, muscle aches, nausea, headache. The patient did not receive any treatment for the adverse events. The clinical outcome of the event was recovered on unspecified date in Mar2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718471
Sex: F
Age:
State: TX

Vax Date: 03/26/2021
Onset Date: 03/26/2021
Rec V Date: 09/21/2021
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: UTI; Pulled muscle; Acute right flank pain 5-10 minutes following vaccine. Pain grew in intensity and difficulty breathing was experienced as I drew a breath in. Pain felt like it was stabbing at every intake of breath; Acute right flank pain 5-10 minutes following vaccine. Pain grew in intensity and difficulty breathing was experienced as I drew a breath in. Pain felt like it was stabbing at every intake of breath; Acute right flank pain 5-10 minutes following vaccine. Pain grew in intensity and difficulty breathing was experienced as I drew a breath in. Pain felt like it was stabbing at every intake of breath; This is a spontaneous report from a contactable consumer (patient herself). A 44-years-old non pregnant female patient received first dose of bnt162b2 (Solution injection; Batch/Lot Number: EP6955), via an unspecified route of administration, administered in Arm Right on 26Mar2021 at 09:45 (at the age of 44-years-old) as single dose for covid-19 immunisation. Medical history included hysterectomy, shoulder surgery, right knee scope, benign fatty tissue growth on kidney and allergy to CT contrast dye, tramadol and morphine. The patient's concomitant medications were not reported. The patient previously took morphine and tramadol. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient did not receive within 2 weeks of vaccination. The patient experienced acute right flank pain 5-10 minutes following vaccine. Pain grew in intensity and difficulty breathing was experienced as she drew a breath in. Pain felt like it was stabbing at every intake of breath and mild relief was felt with leaning forward and tension. Three hours post injection, flank pain at a more manageable level and breathing difficulty subsided. Emergency room visit yielded a mild UTI and a pulled muscle. There was no activity which led to this pulled muscle that she could identify. She was feeling great the morning of the vaccine, she was comfortable with needles, did not feel any anxiety before, during or immediately after injection. She was sitting in a waiting area participating in a video conference when onset began. Therapeutic measures were taken as a result of the events. The outcome of the events was recovering. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1718472
Sex: F
Age:
State: NY

Vax Date: 03/28/2021
Onset Date: 03/28/2021
Rec V Date: 09/21/2021
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: Sore arm; felt weak; felt very sleepy; itchiness at injection site; heart palpitations; short of breath feeling like after running; This is a spontaneous report from a contactable consumer or other non-HCP. A 49-year-old female patient received second dose of BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number- UNKNOWN) via an unspecified route of administration on 28Mar2021 as dose 2, single (at the age of 49-years-old) for COVID-19 immunization. Patient was not pregnant at the time of vaccination. Vaccination facility type was reported as School/Student Health Clinic. Patient medical history and concomitant medications were not reported. Patient allergies to food, or other products was reported as unknown. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Historical vaccine included first dose of BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number- UNKNOWN) via an unspecified route of administration on 07Mar2021 as dose 1, single for COVID-19 immunization. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced sore arm, felt weak, felt very sleepy, itchiness at injection site, heart palpitations, short of breath feeling like after running on 28Mar2021. Therapeutic measures taken as a result of sore arm, felt weak, felt very sleepy, itchiness at injection site, heart palpitations, short of breath feeling like after running included Tylenol as treatment medication. The outcome of the events was resolved on an unspecified date in Mar2021. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718473
Sex: F
Age:
State:

Vax Date: 03/24/2021
Onset Date: 03/26/2021
Rec V Date: 09/21/2021
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: her injection site is still bruised; randomly started bleeding a bit/ bleeding at immunization site; This is a spontaneous report from a contactable consumer (Patient) via Regulatory Authority. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: ER8730), via an unspecified route of administration in left arm on 24Mar2021 at 13:00 as dose 1, single for COVID-19 immunisation at clinic. The patient's medical history and concomitant medications were reported as none. The patient's past drug included vitamins. Patient's family medical history relevant to event was reported as none. Patient did not receive any other vaccine within four weeks prior to the first administration date of the suspect vaccine. On 26Mar2021, a couple of days after getting the immunization, the patient's injection site was still bruised. While it was getting better, the bruise persisted and on an unspecified date, in 2021, it randomly started bleeding a bit. Patient's arm did bleed when she got the shot, but then stopped right after. The patient received treatment for the events. The clinical outcome of the events was resolving. No follow-up attempts are possible; Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718474
Sex: M
Age:
State:

Vax Date: 03/01/2021
Onset Date:
Rec V Date: 09/21/2021
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: Vision started to get blurry; Double vision at long distances; Troubles trying to walk; Eyelids are drooping down and are almost closed all the way; This is a spontaneous report from a non-contactable consumer or other non hcp (patient). A male patient of an unspecified age received BNT162b2 (CONMINTARY, Solution for injection, Lot No: was not reported), via an unspecified route of administration on Mar2021 as 1st dose, single for covid-19 immunisation.The patient medical history and concomitant medications were not reported.The patient experienced vision started to get blurry, double vision at long distances, troubles trying to walk, eyelids are drooping down and are almost closed all the way on an unspecified date. Patient wants to know if this is a side effect of the vaccine. The outcome of the events for vision started to get blurry, double vision at long distances was not recovered, troubles trying to walk, eyelids are drooping down and are almost closed all the way was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718475
Sex: F
Age:
State: NY

Vax Date: 03/26/2021
Onset Date:
Rec V Date: 09/21/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: She had arthritis in her knees; This is a spontaneous report received from Regulatory Authority via contactable female consumer (patient). A female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection) via an unspecified route of administration on 26Mar2021 (Batch/Lot number was not reported) as dose 1, single for covid-19 immunisation. The patient's second dose scheduled on 16Apr2021. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient had arthritis in her knees and wanted to know if she could take Ibuprofen or advil. She just wanted to make sure that she would not mess up with the vaccine. The patient had arthritis in her knees on an unspecified date. The outcome of event was unknown. No follow-up attempts are possible. Information on lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718476
Sex: F
Age:
State: PA

Vax Date: 03/18/2021
Onset Date:
Rec V Date: 09/21/2021
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: got her 1st dose on 18MAR2021, and after 2 weeks she has rashes; This is a spontaneous report received from contactable consumer (patient ) via Pfizer sponsor program . A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection batch/Lot number was not reported ,expiry date was not reported), dose 1 via an unspecified route of administration on 18Mar2021 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 got her first dose on 18mar2021, and after 2 weeks she has rashes .Patient asked if it is associated with the covid-19 vaccine because her second dose schedule is on 08Apr2021.Outcome of the event was unknown. No follow-up attempts are possible. Information on lot/batch number cannot be obtained.No further information is expected.

Other Meds:

Current Illness:

ID: 1718477
Sex: F
Age:
State: NJ

Vax Date: 03/28/2021
Onset Date: 03/01/2021
Rec V Date: 09/21/2021
Hospital:

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

Lab Data: Test Date: 20210329; Test Name: temperature; Result Unstructured Data: Test Result:temperature of 99.1 (high); Comments: temperature of 99.1 (high)

Allergies:

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

Symptoms: chills; temperature of 99.1; achiness/Achy the whole; tired; I was little like weak; This is spontaneous report received from Pfizer Sponsored Program. A contactable female consumer (Patient) reported herself. A female patient of an unspecified age received second dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, on 29Mar2021, as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, on an unspecified date, as a single dose for COVID-19 immunization and had injection site pain. The patient received 2nd dose of Pfizer vaccine Sunday March 28th had reactions that lasted until Monday the 29th including: a temperature of 99.1 which lasted a few hours, chills, achiness, tired on an unspecified date in Mar2021. The side effects started quicker than when receiving the 1st dose, at which time she had injection site pain and muscle pain. Overall a feeling of being slightly unwell. The patient would like to know how long they should quarantine before seeing friends and family. The patient stated, "she just had her second dose of Pfizer she did have reaction 'actually' that after noon, she had it in the morning and it lasted until, she had it Sunday, Monday night, even yesterday she was little like weak and whatever but no fever no nothing. She had 98.9 which was really not a fever. Chills, achy the whole you know, not nauseous, no diarrhea but just very achy and chill. She had a really silly question on she had it obviously this week was there a quarantine. If the patient didn't stay at quarantine but it didn't say not to. So she was not sure what to do. Her husband and she both had the second dose. The patient underwent lab test and procedure included Body temperature with temperature of 99.1 (high) on 29Mar2021. Outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718478
Sex: F
Age:
State:

Vax Date: 02/01/2021
Onset Date:
Rec V Date: 09/21/2021
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 Name: platelets; Result Unstructured Data: Test Result:low

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: unwell; low platelets; fatigue; low grade fever; decreased appetite; This is a spontaneous report from a contactable consumer or other non hcp. A female patient of an unspecified age received bnt162b2 (BNT162B2, Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on an unspecified date as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunisation; Lenvatinib mesilate (LENVIMA), via an unspecified route of administration from 01Feb2021 (Batch/Lot number was not reported) to an unspecified date, at 24 mg for an unspecified indication. Medical history included thyroid cancer from an unknown date and unknown if ongoing, decreased appetite from an unknown date and unknown if ongoing, chemotherapy from an unknown date and unknown if ongoing, smoking cessation therapy from an unknown date to Sep2020 (quit 9/2020). The patient's concomitant medications were not reported. The patient experienced unwell on an unspecified date with outcome of unknown, low platelets on an unspecified date, fatigue on an unspecified date, low grade fever on an unspecified date, decreased appetite on an unspecified date. The patient underwent lab tests and procedures which included platelet count: low on. The action taken in response from Lenvatinib mesilate was unknown. The outcome of the events malaise, platelet count decreased, fatigue, pyrexia, decreased appetite was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds: LENVIMA

Current Illness: Smoking cessation therapy ((quit 9/2020))

ID: 1718479
Sex: M
Age:
State: GA

Vax Date: 01/12/2021
Onset Date: 01/01/2021
Rec V Date: 09/21/2021
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: pain in the shoulder; constant headache; shortness of breath; Dizziness; I had the double vision; saw 2 images of the same; only in the left eye; I am not sure if could see; deep cough and then I expectorate or spit a very very medium brown material, very thick; Cough; Sore throat; I could not walk between chair and sofa; This is a spontaneous report from a contactable consumer. This 72-years-old male consumer (patient) reported for himself that: A 72-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/Lot Number: EL0142; Expiration Date: 20Mar2021), via an unspecified route of administration on 12Jan2021 (at the age of 72-year-old) as single dose for covid-19 immunisation. Medical history included Heart condition, diabetes mellitus, I had multiple strokes, I had a pacemaker, I had 4-way bypass and I had some MIs, TIAs and A-fib from an unknown date and unknown if ongoing and he is taking probably 8 to 10 different medication. Patient received unspecified concomitant medication. Patient stated, start with pain in the shoulder, that lasted about 3 days after the shot and then also pretty much the constant headache, shortness of breath, so dizzy that I could not walk between chair and sofa, I do not drive right now because of that, I had the double vision, I actually saw 2 images of the same about I guess we call theoretical maybe inch apart, and that is only in the left eye and it only occurred for about 25 minutes, I am not sure if could see. when I wake up in the morning I had very deep cough and then I expectorate or spit a very very medium brown material, very thick. patient stated still experiencing the events, I do not know because just really late specially the dizziness, and the cough and the sore throat. No lab test was performed. Patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/Lot Number: EL9263; Expiration Date: 31May2021), via an unspecified route of administration on 02Feb2021 as single dose for covid-19 immunisation. The outcome of the events was reported as not recovered. No Follow-up attempts are possible. No Further Information is expected. .

Other Meds:

Current Illness:

ID: 1718480
Sex: F
Age:
State: PA

Vax Date: 04/10/2021
Onset Date: 04/11/2021
Rec V Date: 09/21/2021
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: mild difficulty breathing; localized rash; itching at injection site; Soreness in arm progressively worse right after injection; muscle pain all over; chills; fever; debilitating weakness; numbness in my arm; stiffness in my neck; dizziness; balance difficulty; This is a spontaneous report from a contactable consumer (patient). A 66-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: Unknown), via an unspecified route of administration, on 10Apr2021 at 10:00 (at the age of 66-years-old), in right arm as dose 2, single for COVID-19 immunization in other facility. Medical history included latex (known allergies: latex) and shellfish (known allergies: shellfish). Concomitant medications were not reported. Historical Vaccination reported as BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: Unknown), via an unspecified route of administration, on 20Mar2021 (at the age of 66-years-old), in right arm as dose 1, single for COVID-19 immunization in other facility. COVID prior vaccination reported as no and COVID tested post vaccination reported as no. Other medications in two weeks reported as no. On 11Apr2021 13:00 the patient experienced mild difficulty breathing, localized rash, itching at injection site, soreness in arm progressively worse right after injection, muscle pain all over, chills, fever, debilitating weakness, numbness in my arm, stiffness in my neck, dizziness, balance difficulty. Treatment was not taken for the events. The outcome of the events was recovering. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1718481
Sex: F
Age:
State: MA

Vax Date: 03/07/2021
Onset Date: 03/15/2021
Rec V Date: 09/21/2021
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: shingles; Decreased breast milk supply; Decreased breast milk supply; Decreased breast milk supply; This is a spontaneous report from a contactable consumer. A 28-year-old female patient (non-pregnant) received BNT162B2 (BNT162B2, PFIZER BIONTECH, COVID-19 Vaccine, Solution for injection: Batch/Lot number: EN6203, and expiration date: Not reported), via an unspecified route of administration, administered in Arm Left on 07Mar2021 as DOSE 2, SINGLE (age at vaccination 28-year-old) for covid-19 immunisation. The patient medical history included hypothyroidism, Tree Nuts allergy. Concomitant medication included ascorbic acid, betacarotene, calcium sulfate, colecalciferol, cyanocobalamin, ferrous fumarate, folic acid, nicotinamide, pyridoxine hydrochloride, retinol acetate, riboflavin, thiamine mononitrate, tocopheryl acetate, zinc oxide (PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS FUMARATE;FOLIC ACID;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RETINOL ACETATE;RIBOFLAVIN;THIAMINE MONONITRATE;TOCOPHERYL ACETATE;ZINC OXIDE]) taken for an unspecified indication, start and stop date were not reported; levothyroxine taken for an unspecified indication, start and stop date were not reported. The patient historical vaccine includes BNT162B2 (BNT162B2, PFIZER BIONTECH, COVID-19 Vaccine, Solution for injection: Batch/Lot number: EL9266, and expiration date: Not reported), via an unspecified route of administration, administered in Arm Left on 14Feb2021 at 11.30AM as DOSE 1, SINGLE for covid-19 immunisation. other vaccine in four weeks: No. covid prior vaccination was No. covid tested post vaccination was No. It was reported that happen only after my second dose of the vaccine. I have a few close friends (2-3) who are also breastfeeding, and they also reported changes in breastmilk supply to the point that they switched to formula. Thankfully, I was able to pick up my supply again through pumping a ton, but they reported not being able to get back to their normal supply after the vaccine, also was diagnosed with shingles on 01Apr2021, 3.5 weeks after my second vaccine. I'm not sure if this has been reported by anyone else, but I think it's pretty bizarre that I got the shingles at such a young age and in less than 4 weeks from getting the vaccine. Therapeutic measures were taken as a result of shingles, decreased milk supply. The outcome of the event was suppressed lactation and herpes zoster was recovering. No follow up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021423510 same reporter/drug, different event/Patient (baby case)

Other Meds: PRENATAL VITAMINS [ASCORBIC ACID;BETACAROTENE;CALCIUM SULFATE;COLECALCIFEROL;CYANOCOBALAMIN;FERROUS ; LEVOTHYROXINE

Current Illness:

ID: 1718482
Sex: F
Age:
State: CA

Vax Date: 04/02/2021
Onset Date: 04/03/2021
Rec V Date: 09/21/2021
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: Started with a pulled muscle sensation next day; chest pain on right upper chest; Very difficult to breath or move; Very difficult to breath or move; Pain became very severe; felt like what sounded like a snap in neck and was unable to move head; feeling slight pain in chest and behind neck and back of head; feeling slight pain in chest and behind neck and back of head; This is a spontaneous report from a contactable consumer (patient). A 48-years-old non-pregnant female patient (not pregnant at the time of vaccination) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 Vaccine, solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration administered in Left arm on 02Apr2021 at 02:45 pm (48-year-old at the time of vaccination) as dose 1, single for covid-19 immunisation. Medical history included Hay Fever, Hashimotos and Graves Disease from an unknown date and unknown if ongoing. The patient had no known allergies. The patient had not received any vaccine within four weeks. The patient had no covid prior to vaccination. The patient was not tested since vaccination. The patient had no other medications in two weeks. On 03Apr2021 at 12:00 PM, the patient experienced a pulled muscle sensation, chest pain on right upper chest, very difficult to breath or move, severe pain, a snap in neck, was unable to move head, slight pain in chest and behind neck and back of head. It started with a pulled muscle sensation next day after the vaccine which lasted 2 days. On 3rd day, the patient began having chest pain on right upper chest. Pain became very severe. On 6th day, the patient felt like what sounded like a snap in neck and was unable to move head. Pain was also very severe. Now almost a week after symptoms began the patient was still feeling slight pain in chest and behind neck and back of head. The patient was not sure if it was vaccine driven but cannot think of anything else. The outcome of events were not recovered. Information about Lot/Batch number has been requested. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1718483
Sex: M
Age:
State: NC

Vax Date: 03/20/2021
Onset Date:
Rec V Date: 09/21/2021
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: Migraine; double vision; droopy eyelid; This is a spontaneous report from regulatory authority. A contactable male consumer (patient) reported for himself. A male patient of unspecified age received first dose of bnt162b2 (Pfizer Covid-19 Vaccine, Solution for injection), via an unspecified route on 20Mar2021, as a single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. On an unknown date, patient experienced migraine, double vision, and droopy eyelid after he took the 1st dose. Patient would like to know what are the side effects of the vaccine before he will take the 2nd dose. The 2nd dose should be today, 10Apr2021, but the patient rescheduled the 2nd dose. The clinical outcome of the events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1718484
Sex: F
Age:
State: OH

Vax Date:
Onset Date:
Rec V Date: 09/21/2021
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: Tiredness; cough; difficulty breathing; This is a spontaneous report from a contactable consumer or other non hcp. A 24-years-old non pregnant female patient received (BNT162B2, formulation: Solution for injection, Lot Number: unknown), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as DOSE 1, SINGLE for COVID-19 immunisation. The patient medical history was not reported Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. and concomitant medications were not reported. The patient experienced tiredness, cough and difficulty breathing on an unspecified date. The clinical outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No follow-up attempts are possible.

Other Meds:

Current Illness:

ID: 1718485
Sex: F
Age:
State: FL

Vax Date: 04/14/2021
Onset Date: 04/15/2021
Rec V Date: 09/21/2021
Hospital:

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

Lab Data: Test Date: 20210415; Test Name: Heart rate; Result Unstructured Data: Test Result:high/over 100 beats per minute

Allergies:

Symptom List: Vomiting

Symptoms: High heart rate while at rest, over 100 beats per minute with palpitations; High heart rate while at rest, over 100 beats per minute with palpitations; shortness for breath.; This is a spontaneous report from a contactable consumer (Patient). A 36-years-old female patient (patient was not pregnant at the time of vaccination) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: unknown, Expiration date: unknown), dose 2 via an unspecified route of administration in arm left on 14Apr2021 at 10:30 (age at vaccination was 36 years) as single dose for COVID-19 immunization. The patient's medical history included COVID-19 from an unknown date. The patient did not have any known allergies. Concomitant medication included loratadine, pseudoephedrine sulfate (CLARITIN D 12 HOUR) in two weeks. The facility where the most recent COVID-19 vaccine was administered was unknown county. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 15Apr2021 at 11:00, after first dose the patient experienced high heart rate while at rest, over 100 beats per minute with palpitations and shortness for breath. No treatment was received for the adverse events. The patient underwent lab tests and procedures which included heart rate: high/over 100 beats per minute on 15Apr2021. Patient visits healthcare professional office/clinic visit, Emergency room/department or urgent care. No treatment received for the adverse events. The outcome of the events was resolving. Information about Lot/Batch number is requested. Follow-up (17Sep2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made.

Other Meds: CLARITIN D 12 HOUR

Current Illness:

ID: 1718486
Sex: F
Age:
State: FL

Vax Date: 04/14/2021
Onset Date: 04/15/2021
Rec V Date: 09/21/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: Herpes; fever; lethargy; muscle weakness; This is a spontaneous report from a contactable consumer (patient herself). A 42-years-old non pregnant female patient received 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 14Apr2021 10:00 (age at vaccination: 42 years) as DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history were not reported. There were no concomitant medications. The patient had no known allergies. The patient did not have any other vaccine in four weeks not received ant medications in 2 weeks. On 15Apr2021, the patient experienced herpes, fever, lethargy and muscle weakness. The adverse event resulted in physician's office visit. The patient received Advil as treatment for the adverse event was advised to rest. The patient had no prior vaccination for covid nor was tested post vaccination. The outcome of all the events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1718487
Sex: F
Age:
State: MS

Vax Date: 02/25/2021
Onset Date: 04/04/2021
Rec V Date: 09/21/2021
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: Back pain, Cold sweat, Headache, Nausea, Vomiting

Symptoms: Shingles; This is a spontaneous report from a contactable consumer. A 45-year-old non pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for Injection, Batch/Lot number: EN6201, Expiration date: Not reported) (at the age of 45-year-old) via an unspecified route of administration, administered in Arm Right on 25Feb2021 15:00 as DOSE 2, SINGLE and first dose received on 02Feb2021 at 10:00 AM (Lot number: EZ9264) (at the age of 45-year-old) for covid-19 immunisation. Concomitant medications included estrogens conjugated (PREMARIN); erenumab aooe (AIMOVIG). The patient's medical history was not reported. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 04Apr2021 at 12:00 the patient experienced shingles (herpes zoster). AE resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Therapeutic measures were taken as a result of shingles. Patient received treatment of IV medications in ER, multiple medications. The outcome of the event was resolving. No follow-up attempts are possible. No further information is expected.

Other Meds: PREMARIN; AIMOVIG

Current Illness:

ID: 1718488
Sex: F
Age:
State: IL

Vax Date: 04/16/2021
Onset Date: 04/18/2021
Rec V Date: 09/21/2021
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: full blown torso front and back; body rash; shingles; very achy; This is a spontaneous report from a contactable consumer (patient). A 48-year-old non-pregnant female patient (not pregnant at the time of vaccination) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number: Unknown), via an unspecified route of administration in right arm on 16Apr2021 at 03:30 AM (at the age of 48 years old) as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunisation. Medical history included post-traumatic stress disorder, neoplasm malignant, anxiety. The patient did not have any known allergies. Concomitant medications in two weeks included ciprofloxacin (CIPROFLOXACIN) for herpes zoster; ethinylestradiol, norgestimate (SPRINTEC); oxcarbazepine (OXCARBAZEPINE); lorazepam (LORAZEPAM). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient received first dose of unspecified vaccine on 16Apr2021. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. On 18Apr2021 at 21:30 patient experienced very achy sat. Sun. She woke up with a questionable patch on her abdomen sat. She didn't think related. Sore rash like. She had a full blown torso front and back body rash on sun night. She got cream. Later in the week diagnosed with shingles. She have cancer so not sure what to attribute the shingles to. The event resulted in doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of very achy, cream for body rash, valacyclovir for shingles. The outcome of events was recovering.

Other Meds: CIPROFLOXACIN; SPRINTEC; OXCARBAZEPINE; LORAZEPAM

Current Illness:

ID: 1718489
Sex: F
Age:
State: WI

Vax Date: 04/23/2021
Onset Date: 04/24/2021
Rec V Date: 09/21/2021
Hospital:

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

Lab Data: Test Date: 20210424; Test Name: fever; Result Unstructured Data: Test Result:fever; Comments: Time: 09:00 am

Allergies:

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

Symptoms: fever; Vomiting; double vision; body aches; This is a spontaneous report from a contactable consumer or other non-healthcare professional (patient). A 55-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot Number: EN6198), dose 1 via an unspecified route of administration, administered in right arm on 23Apr2021 at 10:45 (at the age of 55-year-old) as dose 1, single for COVID-19 immunisation. Medical history included multiple sclerosis from an unknown date and unknown if ongoing, COVID-19 from an unknown date and unknown if ongoing. No known allergies were reported. There were no concomitant medications. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was diagnosed with COVID-19 prior to vaccination. The patient had not been tested for COVID-19 since the vaccination. On 24Apr2021 at 09:00, the patient experienced fever, vomiting, double vision, body aches. The patient underwent lab tests and procedures which included body temperature: fever on 24Apr2021 at 09:00. No treatment was received for the events. The outcome of the events was reported as resolving. No Follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1718490
Sex: M
Age:
State: WA

Vax Date: 04/17/2021
Onset Date: 04/18/2021
Rec V Date: 09/21/2021
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: Golf ball sized lump developed at injection site about 24 hours/Lump is raised about 1 cm and itchy; Golf ball sized lump developed at injection site about 24 hours/Lump is raised about 1 cm and itchy; This is a spontaneous report from a contactable consumer. This 33-year-old male consumer (Patient) reported that. A 33-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: Ew0162), dose 1 via an unspecified route of administration, administered in Arm Left on 17Apr2021 12:30 as (At the age of 33-years) dose 1, single for covid-19 immunisation. Nonmedical history was not reported. There were no concomitant medications. No other vaccine in four weeks. No Other medications in two weeks. No COVID prior vaccination. No COVID tested post vaccination. No Known allergies ware reported. On 18Apr2021 12:30 patient experienced Golf ball sized lump developed at injection site about 24 hours. Lump is raised about 1 cm and itchy. Has been present for 10 days and counting. Patient was not received any treatment for events. The outcome events was not recovered at the time of report. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am