VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 11/12/2021
** VAERS DATABASE Last updated: November 12, 2021**
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Manufacturers

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

COVID19 Lot Number

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

Incidents per State

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

ID: 1683782
Sex: M
Age:
State: CT

Vax Date: 02/11/2021
Onset Date: 02/12/2021
Rec V Date: 09/08/2021
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: Chills; Soreness at injection site; Headache (migraine like); This is a spontaneous report from a contactable consumer (Patient). A 48-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; solution for injection, Lot Number: EL3247), via an unspecified route of administration on 11Feb2021 10:30 AM (at the age of 48-year-old) as a dose number unknown, single for COVID-19 immunization. The patient medical history and concomitant medication were not reported. The patient did not receive any other vaccines within four weeks. Patient does not have COVID prior vaccination and was not tested to COVID post vaccination. Patient had no known allergies. On 12Feb2021 12:00 AM the patient experienced chills, Soreness at injection site, Headache (migraine like). Patient had not received any treatment for the events reported. The outcome of the events was recovered on unspecified date in 2021. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1683783
Sex: F
Age:
State: NJ

Vax Date: 02/14/2021
Onset Date: 02/15/2021
Rec V Date: 09/08/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: dizziness; Orthostatic hypotension; This is a spontaneous report from a contactable Nurse (Patient). A 66-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number N6201) via an unspecified route of administration, administered in arm left on 14Feb2021 17:00 (age at vaccination 66 years) as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced dizziness and orthostatic hypotension both on 15Feb2021 06:15. It was reported as patient received the Pfizer vaccine yesterday 14Feb2021 and experienced dizziness and stated that dizziness was listed as a severe reaction to the covid 19 vaccine and wanted to know if there have been any reports of dizziness. Patient felt kind like orthostatic hypotension. The outcome of the events was not recovered. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1683784
Sex: F
Age:
State: MD

Vax Date: 02/10/2021
Onset Date: 02/14/2021
Rec V Date: 09/08/2021
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: Test Date: 20210214; Test Name: blood pressure; Result Unstructured Data: Test Result:141/85; Comments: Her pressure yesterday was 141/85; Test Date: 20210215; Test Name: blood pressure; Result Unstructured Data: Test Result:179/105; Comments: This morning it was 179/105.

Allergies:

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

Symptoms: her blood pressure has been slowly going up; This is a spontaneous report from a contactable consumer (patient). A 90-years-old female patient received bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, solution for injection), dose 2 via an unspecified route of administration, administered in Arm Left on 10Feb2021 (at the age of 90-years-old) (Batch/Lot Number: EL9263; Expiration Date: 31May2021) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included macular degeneration from 2005 and ongoing. The patient's concomitant medications were not reported. Patient previously took first dose of bnt162b2 (Batch/Lot Number: EL3248; Expiration Date: 30Apr2021) administered in left arm on 20Jan2021 for covid-19 immunisation. The caller reported that her blood pressure had been slowly going up a little bit on 14Feb2021. It was reported that her blood pressure was 141/85 yesterday on 14Feb2021. On 15Feb2021 in morning, her blood pressure was fluctuating and it was 179/105. Patient did not receive additional vaccines on same date of the Pfizer suspect. Prior Vaccinations (within 4 weeks) was reported as Covid-19 vaccine. Outcome of the event was not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness: Macular degeneration

ID: 1683785
Sex: M
Age:
State: NV

Vax Date: 02/11/2021
Onset Date: 02/12/2021
Rec V Date: 09/08/2021
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: He described his reaction as something that was more or less like diarrhea, except that the only thing coming out was mucus.; He described his reaction as something that was more or less like diarrhea, except that the only thing coming out was mucus./he started having discharge through his rectum, like a mucous, no color to it; It did not stop until Sunday afternoon when his bowel movement returned to normal.; This is a spontaneous report from a contactable Consumer. An 81-years-old male patient reported himself that he received first dose of BNT162B2 (Pfizer-BioNTech COVID-19 Vaccine, formulation: Solution for injection, batch/lot number: EL9267) via an unspecified route of administration on 11Feb2021, Thursday at around 09:00 AM (at the age of 81-year-old) as DOSE 1, SINGLE for COVID-19 immunisation. The patient did not have medical history. The concomitant medications were not reported. The patient did not experience a reaction until Friday noon. On 12Feb2021, Friday around noon, the patient started having discharge through his rectum, like a mucous, no color to it. He described his reaction as something that was more or less like diarrhea, except that the only thing coming out was mucus. It did not stop until Sunday afternoon when his bowel movement returned to normal. On, Saturday morning the patient called a nurse through his insurance and she basically said if it does not don't go away call doctor Monday morning and made an appointment. On Saturday afternoon the patient had one little movement that was a little brown in color then it went right back to liquid, he could not stop it anytime gas came out or anything he couldn't stop it and that went on until noon Sunday and at noon on Sunday he had a movement, a little movement again which was brown and now it seems like it is back to normal. The patient did not know whether or not go see a doctor, he wanted to see if anyone has reported this before with the vaccine. He did not really know what he was trying it say but he wanted to try to find out if it was a reaction so he would know whether or not he can expect it the second time. At the time of this reported the discharge had resolved. The outcome of the events was recovered on an unspecified date in Feb2021. Follow-up attempts were completed. No further information was expected.

Other Meds:

Current Illness:

ID: 1683786
Sex: M
Age:
State:

Vax Date: 02/01/2021
Onset Date:
Rec V Date: 09/08/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: This is a spontaneous report from contactable consumer (patient). A male patient received the second dose of BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine, solution for injection, batch/lot# not reported, expiry date: unknown), via an unspecified route of administration on an unspecified date, in Feb 2021, single dose, for COVID-19 immunization. Patient's medical history included inflammation from tumors in his neck (receiving chemotherapy and often gets congestion that interferes with breathing). Concomitant medications not reported. The patient reported, he had both shots. The last was 13 days ago. He wants to take an antibiotic but wanted to make sure it won't hamper with the vaccine. He reports these symptoms as normal for him but reports his only side effects from the vaccine was "it felt like someone took a baseball bat to my arm afterwards," on an unspecified date. Outcome of the event: unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1683787
Sex: M
Age:
State:

Vax Date: 02/13/2021
Onset Date: 02/01/2021
Rec V Date: 09/08/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: felt a little bit of soreness.; This is a spontaneous report from a contactable consumer (patient) via Medical Information team. A 73-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported, Expiry date: Unknown) via an unspecified route of administration on 13Feb2021 (at the age of 73-year-old) as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications was not reported. In Feb2021, he felt "a little bit of soreness" within 12 from receiving the Pfizer-BioNTech COVID-19 Vaccine. He is currently fine. He is scheduled on 26Feb2021 for a dental appointment to remove a temporary crown. He mentioned that he would be given a local anesthesia, and asked if this would have any interaction with the vaccine. The outcome of the event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683788
Sex: F
Age:
State: MD

Vax Date: 01/30/2021
Onset Date: 02/03/2021
Rec V Date: 09/08/2021
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 Name: Height; Result Unstructured Data: Test Result:shrunk; Comments: She shrunk a lot, currently about 5 ft.

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: never been so sick in her life; She shrunk a lot, currently about 5 ft.; severe headache; felt like her eyes would jump out of her head; About 4-5 hours later, on 04Feb2021 patient threw up nothing but bile; She felt bad all over; really bad, bad stomach pains; This is a spontaneous report from a contactable consumer (patient). A 89-years-old female patient received bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: EL9264, Expiration date: unknown), via an unspecified route of administration, administered in right arm on 30Jan2021 11:30 (at the age of 89 years) as dose 1, single for covid-19 immunization. Patient medical history included spinal fracture (Spine broken 3 times), unspecified surgery (6 surgeries. Onset prior to Pfizer COVID-19 Vaccine), only about 1/3 kidney function (Onset prior to Pfizer COVID-19 Vaccine), Chronic lungs (Onset prior to Pfizer COVID-19 Vaccine), enlarged heart (Onset prior to Pfizer COVID-19 Vaccine), acid reflux and sleep disorder. The ongoing medical history included cancer from 2011 (Has been fighting 3 types of cancer; cancer has been growing for last 10 years. She has had all kinds of chemicals put into her body. Onset prior to Pfizer COVID-19 Vaccine). Concomitant medications included calcium with magnesium and zinc; menaquinone-7 (VITAMIN K 2); bifidobacterium infantis, lactobacillus acidophilus (PROBIOTIC [BIFIDOBACTERIUM INFANTIS; LACTOBACILLUS ACIDOPHILUS]); folic acid, cyanocobalamin (VITAMIN B 12 [CYANOCOBALAMIN]); vitamin b6; cannabidiol (CBD OIL), all for unknown indications; vitamin c [ascorbic acid] taken for an unspecified indication from 25Jan2021 and was ongoing; vitamin d3 taken for an unspecified indication from 18Jan2021 and was ongoing; alprazolam taken for sleep disorder, biotin; selenium; chromium picolinate; unknown product taken as needed under the tongue for nausea; betaine hydrochloride, bromelains, pancreatin, papain, pepsin (SUPER ENZYME) and ammonium chloride, betaine hydrochloride, pancreas extract, pancreatin, pepsin, spleen, stearic acid (ZYPAN), both taken for acid reflux disease. On 03Feb2021, the patient experienced really bad, bad stomach pains. It was reported that, patient finally went to bed because she could not stand the pain of stomach pains anymore and she was hoping the next morning stomach pains would be gone. On 04Feb2021 morning, on waking up patient had severe headache that felt like her eyes would jump out of her head. Patient felt bad all over. About 4-5 hours later, on 04Feb2021 patient threw up nothing but bile. Patient had never been so sick in her life as she was with this reaction. On an unknown date, patient was shrunk a lot, currently about 5 ft. The patient underwent lab tests and procedures which included body height: shrunk, she shrunk a lot, currently about 5 ft. Therapeutic measures were taken as a result of severe headache and patient took nauseous medicine under the tongue which not only did that help some but it relieved her headache a little bit. It was reported that, primary care physician suggested the patient, to take 2 Tylenol in an hour and could do that every 4 hours and that did help the patient. The clinical outcome of events really bad, bad stomach pains and felt like her eyes would jump out of her head was not recovered and outcome of rest all other events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds: VITAMIN K 2; PROBIOTIC [BIFIDOBACTERIUM INFANTIS;LACTOBACILLUS ACIDOPHILUS]; FOLIC ACID; VITAMIN B 12 [CYANOCOBALAMIN]; BIOTIN; SELENIUM; CHROMIUM PICOLINATE; SUPER ENZYME; VITAMIN B6; CBD OIL; VITAMIN C [ASCORBIC ACID]; ZYPAN; VITAMIN D3;

Current Illness: Cancer (fighting 3 types of cancer; cancer has been growing for last 10 years. Onset prior to vaccine)

ID: 1683789
Sex: F
Age:
State: SC

Vax Date: 02/04/2021
Onset Date: 02/04/2021
Rec V Date: 09/08/2021
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: Headaches still to this day; nausea; vomiting; chills; injection site pain for over a week; not feeling good; tired; This is a spontaneous report from a contactable consumer or other non hcp (Patient). A 70-years-old non pregnant female patient received bnt162b2 (BNT162B2, Solution for injection, Lot Number: not reported), via an unspecified route of administration, administered in Arm Left on 04Feb2021 12:00 (at the age of 70 years-old) as dose 1, single for covid-19 immunisation. Medical history included HBP from an unknown date and unknown if ongoing. 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 experience any known allergies. Concomitant medications included amlodipine, zinc, vitamin d3, vitamins taken for an unspecified indication, start and stop date were not reported. On 04Feb2021 14:00, the patient experienced headaches still to this day, nausea, vomiting, chills, not feeling good, tired, injection site pain for over a week and the patient reported just don't feel good. The patient did not receive any treatment for the events. The outcome of the event injection site pain for over a week was recovered on 12Feb2021 while other events were not recovered. Information about lot/batch number has been requested. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Other Meds: AMLODIPINE; ZINC; VITAMIN D3

Current Illness:

ID: 1683790
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/08/2021
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: Wounds on her legs; This is a spontaneous report from a contactable consumer or other non hcp(patient). A 61-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE,solution for injection,Lot number-Not reported), via an unspecified route of administration on an unspecified date as DOSE 1,SINGLE for covid-19 immunisation .Medical history included rheumatoid arthritis, immunosuppression, toe operation , diabetes mellitus , neoplasm , wound infection staphylococcal from an unknown date and unknown if ongoing.The patient's concomitant medications were not reported. On an unspecified date, patient was a 61 year old female who go the first dose of the Pfizer Covid 19 vaccine. She has a home health nurse that comes in 3 times per week due to wounds on her legs that are trying to heal. She also has RA, so her immune system is already compromised. If someone is on antibiotics will it effect the vaccine? She's not taking an antibiotic now, but sometimes she does because of prior MRSA. Will the vaccine effect my wound healing. She is not in a immunosuppressive medication now but previously took a medication for RA and she lost toes due to diabetes and has tumors in her neck because of it. She did not give the name of the medication. The outcome of event was recovering. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683791
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/08/2021
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: she had diarrhea; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, lot number and expiration date were not reported), via an unspecified route of administration on an unspecified date as dose 1, single and bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, lot number and expiration date were not reported), via an unspecified route of administration on an unspecified date as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that patient wanted to report the side effects she had after receiving the first and second dose of Pfizer COVID-19 vaccine. She read the prescribing information sheet but the side effect she had was not listed. Patient did not have any questions she was just calling to report the side effect. She said 2 days after receiving the first dose she had diarrhea for a day and the same thing happened after the second dose. The outcome of the event was recovered on an unspecified date. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683792
Sex: F
Age:
State:

Vax Date: 02/09/2021
Onset Date: 02/01/2021
Rec V Date: 09/08/2021
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: Caller is reporting tiredness; I've not been able to do anything.; Caller reports that her brain was in a fog and she was not able to process anything.; she is a little anxious about it; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 65-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration on 09Feb2021 (Batch/Lot number was not reported) as dose 2, single for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient previously received dose 1 of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unknown date (Batch/Lot number was not reported) as dose 1, single for covid-19 immunization. Caller reported that she was perfectly fine after receiving the first dose of the vaccine. Caller was reporting tiredness that started on Thursday around noon (11Feb2021). On an unspecified date in Feb2021, caller stated that she was not been able to do anything. She had been in bed since then and very distressed about it. Caller reported that her brain was in a fog and she was not able to process anything. As of 14Feb2021 night and this morning 15Feb2021, caller reported that her brain to be much less foggy, but her fatigue was overwhelming both mentally and physically. Caller stated that she became physically tired out within 5 minutes and she was a little anxious about it. The clinical outcome of the event tiredness was not recovered and brain was in a fog was recovering whereas outcome of the other events were unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683793
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/08/2021
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: This is a spontaneous report from a contactable consumer (patient). A female patient, of an unspecified age, received the first dose of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, solution for injection, batch/lot# not reported), via an unspecified route of administration, on an unspecified date, single dose, for COVID-19 immunisation. The patient's medical history and concomitant medications not reported. The patient experienced a headache on an unspecified date. The patient reported she received a dose of Pfizer-BioNTech COVID-19 vaccine on Saturday and has had a headache since then. She wanted to know if this was normal, and if she can take anything to treat the headache (that seems to be a result of the Pfizer-BioNTech COVID-19 vaccine). She inquired whether any there were any contraindications with the fentanyl patch she uses. She wanted to know if she could use antipyretics before or after vaccination with the Pfizer-BioNTech COVID-19 vaccine. Outcome of the event: unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1683794
Sex: F
Age:
State: OH

Vax Date: 01/23/2021
Onset Date:
Rec V Date: 09/08/2021
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: Sore arm; This is a spontaneous report from a contactable consumer (patient). A 28-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9261), via an unspecified route of administration in arm left on 23Jan2021 15:45 (age at vaccination was 28 Years) as dose 1, single for covid-19 immunisation at school or student health clinic. Medical history included bipolar disorder and bell's palsy (twice). Known allergies were unknown. Concomitant medication(s) received in two weeks included lamotrigine (LAMICTAL), vitamin D NOS, biotin, amfetamine aspartate, amfetamine sulfate, dexamfetamine saccharate, dexamfetamine sulfate (ADDERALL) and birth control; all were taken for an unspecified indication, start and stop date were not reported. No other vaccine was received in four weeks prior to the COVID vaccine. On an unspecified date, the patient experienced sore arm. No covid prior vaccination and no covid tested post vaccination. Outcome of the event was unknown. Follow-up attempts completed. No further information expected.

Other Meds: LAMICTAL; VITAMIN D [VITAMIN D NOS]; BIOTIN; ADDERALL

Current Illness:

ID: 1683795
Sex: F
Age:
State:

Vax Date: 01/07/2021
Onset Date:
Rec V Date: 09/08/2021
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: Test Name: antibodies; Result Unstructured Data: Test Result:negative

Allergies:

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

Symptoms: Epstein Barr Virus; This is a spontaneous report from a contactable other hcp. A 40 (unit not provided) female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 07Jan2021 as dose 1, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date the patient experienced Epstein Barr Virus. She was not able to get scheduled initially as Epstein Barr Virus and possibility of antivirals. The patient underwent lab tests and tested negative for antibody procedure. Patient concerned about administration and efficacy. Outcome of the event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683796
Sex: F
Age:
State: VA

Vax Date:
Onset Date:
Rec V Date: 09/08/2021
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: sore arm; This is a spontaneous report from a contactable consumer (patient) via medical information team. A 72-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/Lot Number was not reported, Expiry date was not reported) via an unspecified route of administration, administered on unknown date (at the age of 72 years old) as DOSE 2, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient and her husband had the Pfizer 2nd covid 19 vaccine, other than a sore arm on an unspecified date, didn't have any other side effects. Wants to know if it was effective. The outcome of the event was unknown. Information about lot/batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1683797
Sex: M
Age:
State: NC

Vax Date: 02/11/2021
Onset Date:
Rec V Date: 09/08/2021
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: he started experiencing some swelling and pain in the arm.; he started experiencing some swelling and pain in the arm.; This is a spontaneous report from a contactable consumer (patient's wife). A male patient of an unspecified age received bnt162b2 (BNT162B2, formulation: solution for injection, Batch/Lot number was not provided) via an unknown route of administration, administered on 11Feb2021 as DOSE 2, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. Historical vaccine included first dose of bnt162b2 as DOSE 1, SINGLE for covid-19 immunisation. It was reported that after received the second dose of the Pfizer vaccine patient was told that it was okay to take pain relievers after vaccination. However, they also heard reports contradicting this saying that it might affect antibody production of the vaccine. Patient took some Aleve since he started experiencing some swelling and pain in the arm. Therapeutic measures were taken as a result of he started experiencing some swelling and pain in the arm. The outcome of events was unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683798
Sex: F
Age:
State: KY

Vax Date: 02/12/2021
Onset Date: 02/12/2021
Rec V Date: 09/08/2021
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: Severe headache on left side of head; Injection site a little sore; This is a spontaneous report from a contactable consumer or other non hcp (patient). A female patient of an unspecified age (age reported as 83; Unit: Unknown) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation solution for injection) via an unspecified route of administration on 12Feb2021 (Batch/Lot number was not reported) as dose 1, single for COVID-19 immunization. The patient medical history was not reported. Concomitant medication(s) included influenza vaccine (INFLUENZA VACCIN) taken for antiviral prophylaxis from Feb2021. It was reported by the patient that she got the first dose of the covid vaccine on 12Feb2021 (Friday) and got a little sore because she also got a flu shot. Since Saturday she got headache in the left side of her head (the side of the body where she got the vaccine) and she would like to know how long it would last and when that would be expected to get better. She said that she took Tylenol last night for this since it is a severe side effect. She does not have an email and did not wish to complete report. No further details provided. The outcome was unknown for the event of vaccination site pain and patient was not recovered from the event of headache. Information on the lot/batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds: INFLUENZA VACCINE.

Current Illness:

ID: 1683799
Sex: F
Age:
State:

Vax Date: 02/08/2021
Onset Date:
Rec V Date: 09/08/2021
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: headache; muscle pain; tender at the injection site; nausea; chills; dizzy; weak; couldn't walk; sore throat; This is a spontaneous report from a contactable Consumer. This (Age:65; Unit: Unknown) female Consumer reported for herself. A 65-year-old female patient received a dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: FL9269, Expiration date: unknown), via unspecified route, administered in left arm on 08Feb2021 (at the age of 65-year-old) as dose 1, single for COVID-19 immunization. The patient medical history includes Hypertension from unspecified date to unknown ongoing and thyroid disorder from unspecified date to unknown ongoing and concomitant medications were not reported but mentioned as taking for thyroid and hypertension. On an unspecified date, after the vaccination, the patient experienced headache, sore throat, the muscle pain. The patient tried to get up off the couch to walk and the patient was so dizzy, the patient was going to fall over. Then the patient got nausea and chills. the patient had the chills so bad; it was that bad that her whole body shook. Now the patient due to get the second shot. She is terrified because most people who got the first shot said all they had pain in the injection area and maybe a slight headache, but they did not have any symptoms like she had. So, if she had those symptoms like that, they say the second shot is worse than the first. The events assessed as non-serious. The outcome of the events was unknown. No follow-up attempts possible. No further information expected. Follow-up (01Apr2021): This follow-up is being submitted to notify that the lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1683800
Sex: F
Age:
State: IL

Vax Date: 02/13/2021
Onset Date:
Rec V Date: 09/08/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: fatigue/super fatigued; chills; sweats; nausea/nauseous; injection site pain; Fatigue worsened; This is a spontaneous report from a contactable consumer or other non hcp. A 62-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/lot number was not reported) via an unspecified route of administration on 13Feb2021 (age at vaccination 62years old) as single dose for covid-19 immunisation. Medical history included covid-19 from Nov2020 to an unknown date. The patient's concomitant medications were not reported. On an unspecified date the patient experienced fatigue/super fatigued, chills, sweats, nausea/nauseous, injection site pain, fatigue worsened. The patient has a Report reference number. She is upset as she has been waiting to 50+ minutes to speak with a Nurse or someone with Medical Experience. She has already gone through a report, she has reference number. She got covid shot. She was positive for covid previously in early Nov2020. She just got the first dose on Saturday 13Feb2021. She experienced injection site pain, was super fatigued, chills, sweats, was nauseous, the fatigue got worse. It was not quite as bad as when she had the actual covid virus in Nov2020. Today she is better. she is supposed to babysit her 2-year-old triplets, she wants to know if having these symptoms after the first dose means that she is contagious. If she goes there and gets her kiddos sick, her daughter will shoot her. The Kid's Mom and Dad had covid. They think 2 of 3 triplets had covid but the paediatrician refuses to test them, the kids have not been tested. She clarifies that she went through the safety report just this morning. She was upset when informed that for her question she would have to be transferred. She spoke to a gentleman prior to this that gave the number and she even spoke to a last prior to this that asked her so many questions when all she wanted was her questions address, she gave the same number. She is upset she was not informed about selecting option 3, She has been going in circles on the phone line. The clinical outcome of the events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1683801
Sex: M
Age:
State: CO

Vax Date: 02/14/2021
Onset Date:
Rec V Date: 09/08/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: arm soreness; chills; tiredness; This is a spontaneous report from a Pfizer-sponsored program CoVAX US Support (Medical information team) from a contactable male consumer. A male patient of unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route on 14Feb2021 as a single dose for covid-19 immunization. The patient medical history was not reported. Concomitant medications included lisinopril 10mg, atorvastatin, montelukast 10mg, omperazole 40mg, tamsulosin 0.4mg, trazadone 50mg and acetylsalicylic acid (ASPIRIN LOW, Bayer). On an unknown date, patient experienced arm soreness, chills and tiredness. He states that he did read that these were common symptoms on the fact sheet and would like to know if he can continue taking his daily prescribed medications (trazadone 50mg, lisinopril 10mg, tamsulosin 0.4mg, bayer low dose aspirin, atorvastatin, montelukast 10mg, omperazole 40mg) after receiving the first dose of the Pfizer COVID-19 vaccine yesterday. The clinical outcome of the events was unknown. Follow-up attempts completed. No further information expected.

Other Meds: LISINOPRIL; ATORVASTATIN; MONTELUKAST; OMEPRAZOLE; TAMSULOSIN; TRAZODONE; ASPIRIN LOW

Current Illness:

ID: 1683802
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/08/2021
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: sore arm; Vestibular headache; nausea; real unsteady on her feet; Vertigo; Upset stomach; Do not feel so well; This is a spontaneous report from a contactable consumer (Patient). A 70-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9264), via an unspecified route of administration on an unspecified date in 2021 as dose1, single for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date in 2021, the patient experienced sore arm, vestibular headache, nausea, real unsteady on her feet, vertigo, upset stomach, do not feel so well. It was reported that patient after first dose on last Wednesday (in 2021) had She reported that beside a "minor sore arm", she "felt fine" on Thursday and Friday. She added she "didn't move off the couch" on Saturday because she had a "vestibular headache and nausea". She specified she was able to "move some" on Sunday but "wouldn't pick up" things on the floor, and felt "real unsteady on her feet". She mentioned she still has her symptoms today and feels "fairly miserable". She explained she is "prone to vertigo" because she has "benign positional vertigo". She asked if this experience was normal to the first dose of the vaccine and if the vaccine emphasizing her condition, the positional vertigo. Consumer stated that she should go on to the portal but to tell the truth she had such bad vertigo. She do not use very much and certainly not sit in the computer. She was fine on Thursday and Friday and Saturday morning she have the worse, severe headache she have ever had, unbelievable vertigo and she have got an upset stomach. So basically, importantly it says that she have just had (incomplete sentence). Her immune system is 'driving' up to the vaccine but she certainly going to get the second shot because COVID gives her more than what she was going (Clarification unknown) through but is this a normal reaction. In response to further probing, consumer stated, she do not feel so well. She do not want to spend another 8 or 10 minutes in answering questions. Events were assessed as non-serious by reporter. Outcome of all events was unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1683803
Sex: F
Age:
State: CA

Vax Date: 02/05/2021
Onset Date: 02/13/2021
Rec V Date: 09/08/2021
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: Severe itching on upper left arm vaccine site a week after receiving injection.; This is a spontaneous report from a contactable consumer reported that. A 79-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 05Feb2021 12:00 (Batch/Lot Number: EN5318) as DOSE 1 SINGLE for covid-19 immunization (Age at vaccination 79-years). The patient past Medical history included High cholesterol from an unknown date and unknown if ongoing, low platelets from an unknown date and unknown if ongoing and intrinsic factor deficiency from an unknown date and unknown if ongoing, Known allergies: Penicillin, Erythromycin and Sulfa from an unknown date and unknown if ongoing. Concomitant medication included metoprolol (METOPROLOL) taken for an unspecified indication, atorvastatin (ATORVASTATIN) taken for an unspecified indication, lactulose (LACTULOSE) taken for an unspecified indication and calcium (CALCIUM) taken for an unspecified indication, the patient previously took erythromycin and experienced drug hypersensitivity. 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 vaccine within 4 weeks prior to covid-19 vaccination. On 13Feb2021 the patient reported severe itching on upper left arm vaccine site a week after receiving injection and Looks like a rash has developed. No treatment was received. The event outcome was Not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds: METOPROLOL; ATORVASTATIN; LACTULOSE; CALCIUM

Current Illness:

ID: 1683804
Sex: F
Age:
State:

Vax Date: 02/13/2021
Onset Date:
Rec V Date: 09/08/2021
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: Soreness at the injection site; This is a spontaneous report from a contactable consumer. This female consumer (patient) reported that. A female patient of an unspecified age received bnt162b2 (Pfizer-Biontech Covid-19 Vaccine) (Formulation: Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 13Feb2021 as dose 2, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient reported that both she and her husband got their second vaccine shot on Saturday and they had no side effects from it except soreness at the injection site on an unspecified date. The outcome of event was unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683805
Sex: M
Age:
State:

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

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: tooth ache; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number was not reported), via an unspecified route of administration as dose 1, single for COVID-19 immunization. Patient medical history was not reported. The patient concomitant medications were not reported. The patient stated he was scheduled for his second dose of the vaccine in two days. The patient asked if he could take Clindamycin, 10-day course for a tooth ache before the vaccine. Patient questioned if any antibiotics interact with the vaccine. He stated that there was no adverse event at the time of reporting and confirmed he would call if there was any adverse event. The event outcome for tooth ache was unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683806
Sex: F
Age:
State: OK

Vax Date: 02/13/2021
Onset Date: 02/14/2021
Rec V Date: 09/08/2021
Hospital:

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

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

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: swelling in her left pointer finger along with black and blue discoloration that is moving down her finger; swelling in her left pointer finger along with black and blue discoloration that is moving down her finger; cant bend finger; This is a spontaneous report from a contactable consumer (Patient). A 61-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN6201), via an unspecified route of administration, administered in Arm Right on 13Feb2021 15:00 (vaccinated at the age of 61-years old) as dose1, single for COVID-19 immunization. The patient medical history was not reported and concomitant medications were none. On 14Feb2021, the patient experienced swelling in her left pointer finger along with black and blue discoloration that is moving down her finger, cant bend finger. It was reported that it's odd to call about the Covid Vaccine. She had the shot Saturday after noon, then late yesterday her left pointer finger was swelling and turning blue, today it is still black, blue, and swollen. Today it has move it down the finger. It doesn't hurt, she notices that she cant bend it as much. She has not injured the finger some other way. initially on Sunday the blue color was on 1 inch from the tip on her finger, and this morning it has moved down to the 2nd crease in her finger, making it now 2 inches down the finger being blackish blue. Patient stated that the temperature of the finger feels normal, as well as her sensation in the finger was also normal, she was able to feel. She stated that the finger turning bluish black has worsened since she notices it has traveled down the. Doctors offices and urgent care are closed due to the weather, but nobody ever contacted her back. She has already reported this to drug safety. She has had no positive covid or antibody test. Her most recent test was 3 weeks ago, being negative. She has had no vaccines on the same day or the 4 week prior to the covid vaccine. Outcome of events was not resolved. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1683807
Sex: F
Age:
State:

Vax Date: 02/15/2021
Onset Date: 02/15/2021
Rec V Date: 09/08/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: headache; dizziness; This is a spontaneous report from a contactable consumer (patient). A 56-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot Number: not reported), via an unspecified route of administration on 15Feb2021 04.00 (at the age of 56-years) as dose 1, single for covid-19 immunization. Patient had no known allergies and no relevant medical history. The patient concomitant medications were not reported. The caller stated that she received first dose of bnt162b2 vaccine this mornings around 4 am and seven hours later she was experiencing a headache and dizziness on 15Feb2021. The outcome of the events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1683808
Sex: F
Age:
State: MS

Vax Date: 02/12/2021
Onset Date: 02/12/2021
Rec V Date: 09/08/2021
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: Dizziness within 2 hours after getting Covid injection. It's been 4 days since getting my shot and I still am having the dizziness.; This is a spontaneous report from a contactable consumer or other non hcp (patient reported for herself). A 73-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation solution for injection) via an unspecified route of administration, administered in Arm Left on 12Feb2021 10:30 pm (Batch/Lot Number: EN6201) as dose 1, single for covid-19 immunization (at the age of 73-years-old). Medical history included rheumatoid arthritis from an unknown date and unknown if ongoing. There were no concomitant medications. Patient had not received any other vaccine in four weeks and had not received other medications in two weeks of vaccination. Patient had no covid prior vaccination and had not been tested for covid post vaccination. Patient had no known allergies. Facility type vaccine was reported as other. It was reported that on 12Feb2021 at 12:00 pm patient had dizziness within 2 hours after getting covid injection. It's been 4 days since getting her shot and she was still am having the dizziness. Patient had not received any treatment for the event. Patient was not recovered from the event. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1683809
Sex: F
Age:
State:

Vax Date: 02/01/2021
Onset Date:
Rec V Date: 09/08/2021
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: Feeling queasy; headache; malaise; pain; This is a spontaneous report from a non-contactable consumer or other non hcp. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/lot number was not reported) dose number unknown via an unspecified route of administration on unspecified date in Feb2021 as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Prior to the covid vaccination was reported as unknown. Covid tested post vaccination was reported as unknown. On an unspecified date the patient experienced feeling queasy, headache, malaise, pain. The clinical outcome of the event was unknown. No follow-up attempts are possible. Information about batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1683810
Sex: M
Age:
State:

Vax Date: 02/01/2021
Onset Date:
Rec V Date: 09/08/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: headache; Myalgia; This is a spontaneous report from a Non-contactable consumer. An unspecified age of male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unknown date Feb2021 as a single dose for COVID-19 immunization.The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced Myalgia, headache.The outcome of the events was unknown. Information on the lot/batch number has been requested

Other Meds:

Current Illness:

ID: 1683811
Sex: F
Age:
State: CA

Vax Date: 12/23/2020
Onset Date: 12/23/2020
Rec V Date: 09/08/2021
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: 20210209; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptom List: Nausea

Symptoms: My left arm and back, injection site, has been hurting since first dose.; My left arm and back, injection site, has been hurting since first dose.; My left arm and back, injection site, has been hurting since first dose.; it was even painful to sleep on and sore to movement; This is a spontaneous report from a contactable other hcp (Nurse) reported for herself. A 41-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number and Expiration date was not reported), via intramuscular, administered in Arm Left on 23Dec2020 10:00 (at the age of 41-years-old) as DOSE 1, SINGLE for covid-19 immunisation. Patient was not pregnant at the time of vaccination. The patient medical history was not reported. No known allergies. Concomitant or other medications in two weeks included none. No other vaccine in four weeks. The patient experienced left arm and back, injection site, had been hurting since first dose, it was even painful to sleep on and sore to movement on 23Dec2020. AE resulted in none of the above (details unspecified). No covid prior vaccination and covid was tested post vaccination. The patient underwent lab tests and procedures which included nasal swab: negative on 09Feb2021. Clinical outcome of events was not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683812
Sex: F
Age:
State: MA

Vax Date: 02/12/2021
Onset Date: 02/12/2021
Rec V Date: 09/08/2021
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: Nausea; Vomiting; 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 Arm Right on 12Feb2021 15:45 at the age of 45 years old (Batch/Lot number was not reported) as DOSE 1, SINGLE for COVID-19 immunization. The patient was not pregnant at time of vaccination. The patient has not been COVID-9 tested since the vaccination. The patient was not diagnosed with COVID-19 prior to vaccination. Medical history included breast cancer from an unknown date treated in 2017, egg, lobster, contrast dye and wasps/hornets allergy from an unknown date. Concomitant medication included tamoxifen, escitalopram, colecalciferol (VITAMIN D), docosahexaenoic acid, eicosapentaenoic acid (OMEGA-3); and bifidobacterium breve, bifidobacterium infantis, bifidobacterium longum, lactobacillus acidophilus, lactobacillus bulgaricus, lactobacillus paracasei, lactobacillus plantarum, streptococcus thermophilus (VISBIOME)' all taken for an unspecified indication, start and stop date were not reported. The patient previously took neomycin and experienced allergy. On 12Feb2021 18:30, the patient experienced nausea and vomiting three hours after getting the first shot, lasting for approximately 4-5 hours on 12Feb2021. No treatment was given to the patient for the events. The outcome of the events was recovered on 12Feb2021. No follow-up attempts are possible. Information about lot/Batch number cannot be obtained. No further information is expected.

Other Meds: TAMOXIFEN; ESCITALOPRAM; VITAMIN D [COLECALCIFEROL]; OMEGA-3 [DOCOSAHEXAENOIC ACID;EICOSAPENTAENOIC ACID]; VISBIOME

Current Illness:

ID: 1683813
Sex: M
Age:
State:

Vax Date:
Onset Date: 02/01/2021
Rec V Date: 09/08/2021
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: abdominal pain; This is a spontaneous report from a non-contactable pharmacist. An adult male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On Feb2021, the patient experienced abdominal pain. The patient did not have COVID prior vaccination. The patient was not COVID tested post vaccination. The patient did not receive treatment for the event. The outcome of the event was recovered. No follow-up attempts are possible. Information about Lot/Batch could not be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1683814
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/08/2021
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: small lump on her left arm where she received the vaccine; This is a spontaneous report from a contactable consumer (patient). This 41-year-old female patient received bnt162b2 (BNT162B2, Pfizer-BioNTech Covid-19 mRNA Vaccine, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date patient experienced small lump on her left arm where she received the vaccine, and it is not a lymph node. The outcome of event was unknown. Information about the Lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683815
Sex: F
Age:
State: NY

Vax Date: 02/14/2021
Onset Date: 02/15/2021
Rec V Date: 09/08/2021
Hospital:

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

Lab Data: Test Date: 20210215; Test Name: blood pressure; Result Unstructured Data: Test Result:unknown results

Allergies:

Symptom List: Tremor

Symptoms: aches and pains; chills; tiredness; under arm swelling/swelling under her arm like the size of an orange/saw on the papers that swollen lymph nodes were a side effect; dull ache under her arm; This is a spontaneous report from a contactable consumer (patient). A 47-years-old female patient received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EL9266; Expiration Date: 31May2021, NDC number was unknown), via an unspecified route of administration, administered in left arm on 14Feb2021 at 13:00 hours as dose 2, single (at the age of 47-years-old) for COVID-19 immunisation. Medical history included diabetes from 2011 to an unknown date, high blood pressure (caused by birth control taken at age 24, unable to provide the name, NDC, Lot or Expiry) from an unknown date and unknown if ongoing and thyroid cancer (has half of a thyroid) from 2011 to an unknown date. Historical vaccine included patient received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EL9262; Expiration Date: 31May2021), via an unspecified route of administration, administered in left arm on 24Jan2021 as dose 1, single (at the age of 47-years-old) for COVID-19 immunisation. Patient had no history of previous immunization with the Pfizer vaccine considered as suspect. Patient received no additional vaccines administered on same date of the Pfizer suspect. Patient stated that she takes a lot of daily medications/concomitant medications but declines to provide details. On 15Feb2021, patient experienced aches and pains, chills and tiredness, under her arm was huge, it was like the size of an orange. Patient saw on the papers that swollen lymph nodes were a side effect. Patient had a dull ache under her arm which caused her to look at her arm. It had not gotten any smaller. Patient saw her doctor yesterday (15Feb2021) for a blood pressure check. The doctor checked her blood pressure on the same arm, and it was not swollen. Patient does not know if that may have something to do with it. Patient feels well rested today (16Feb2021). Patient asked what she should do, was there any treatment recommendations and how long will it last. Patient had no emergency room and physician office visit for the events. No relevant tests were performed for the events. The outcome of chills was recovered on 15Feb2021, tiredness and aches and pains was recovered on 16Feb2021, unknown for under arm swelling/swelling under her arm like the size of an orange/saw on the papers that swollen lymph nodes were a side effect and dull ache under her arm. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1683816
Sex: F
Age:
State:

Vax Date: 01/25/2021
Onset Date:
Rec V Date: 09/08/2021
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: citrus taste" in her mouth; This is a spontaneous report from a contactable consumer (patient). A 77-old female patient (Unit: Unknown) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number: Unknown), via an unspecified route of administration on 25Jan2021 as single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Historical vaccine included first dose of BNT162B2 for covid-19 immunisation. She stated that she received her second dose of the Pfizer BioNTech COVID-19 vaccine on 25Jan2021 and was calling to report a "citrus taste" in her mouth. She would like to know what to do about this side effect. Informed caller that the reported "citrus taste" was not listed as a commonly reported side effect and referred her back to her Health Care Professional for guidance. The reporter considered events as non-serious. The outcome of event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683817
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/08/2021
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: he was sick all night; threw up once or twice; he said his head is aching; aches all over; This is a spontaneous report from a non-contactable consumer (patient's spouse). A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on an unspecified date (lot number and expiry date: unknown) as dose number unknown, single, for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On unspecified date, the patient was sick all night and threw up once or twice. His head was aching, then aches all over. He woke up this morning and spouse gave him 2 Tylenol. Outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1683818
Sex: M
Age:
State: CA

Vax Date: 02/05/2021
Onset Date: 02/11/2021
Rec V Date: 09/08/2021
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: 20210212; Test Name: Temperature; Result Unstructured Data: Test Result:96.7 degrees, 98.6; Test Date: 20210212; Test Name: Temperature; Result Unstructured Data: Test Result:98.6

Allergies:

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

Symptoms: couldn't hardly hear from congestion; voice has changed; tempt reached 96.7 and 98.6; congestion; runny nose; fatigue; tiredness; body ache; Sniffles; This is a spontaneous report from a contactable consumer (Patient) via Medical Information Team. A 72-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EN5318), via intramuscular route of administration in left arm on 05Feb2021 at 16:30 (at the age of 72 years old) as single for covid-19 immunisation. Medical history included heart attack was 20 years ago, neoplasm malignant from 2011 to an unknown date, transient ischaemic attack (TIA) from 2015 to an unknown date. There were no concomitant medications. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive additional vaccines on same date of the Pfizer suspect. On 11Feb2021, about 3:30 in the afternoon, he felt real tired. He went to bed. Then from 12Feb2021 until today, he started taking his temperature. The one point at her forehead, and press the trigger. The lowest temperature reading was 96.7 degrees, and the highest was 98.6 degrees. He had some sniffles on an unspecified date in 2021. On 11Feb2021, he reported he felt fatigue, woke up next morning and tempt reached 96.7 and 98.6, body ache, congestion, runny nose, tiredness (started 11Feb2021, lasted for 3 days) and couldn't hardly hear from congestion. Right now, he has no more sniffles. He was just congested on 12Feb2021. He did have fatigue and body aches the first day. He did have a runny nose for a couple of days, but mainly, starting yesterday on 12Feb2021, on 15Feb2021 his voice has changed. He can hardly hear on 15Feb2021. The caller wanted to know why he can't hear and why his voice changed? Is that part of the symptoms of the COVID-19 vaccine? When probed to determine the outcome of the fatigue and body aches, the caller stated he can run a mile right now. For the last 2 days, he has had no sniffles, just the congestion. Even when blowing his nose, nothing really comes out. He was hoping blowing his nose would open up his ears, like when on a plane and chew gum and it opens ears. The caller explained he has a couple of doctor's appointments coming up, the caller wanted to know can he get bloodwork done? The patient underwent lab tests and procedures which included body temperature: 96.7 degrees, 98.6 on 12Feb2021. No family medical history relevant to adverse events was provided and no relevant tests were performed. The patient did not visit emergency room or physician office. The outcome of congestion was not recovered, tiredness was recovered on 14Feb2021, sniffles was recovered on an unspecified date in 2021, while with other events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683819
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 09/08/2021
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: Blood pressure; Result Unstructured Data: Test Result:elevated

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: blood pressure got elevated; blurred vision; This is a spontaneous report from a contactable female consumer via Medical Information Team. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number: Unknown) and second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection), via an unspecified route of administration on an unspecified date as single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. She has taken both doses of the Pfizer BioNTech COVID-19 vaccine. After the first dose, she called 911, 3 days after the shot because her blood pressure got elevated and she had blurred vision. The paramedics checked her, and she was fine. After the second dose, she got the same reaction but it occurred for a longer period and she went to urgent care. She said that she has already notified Pfizer about these adverse events. Despite these reactions, she said that she likes the Pfizer COVID-19 vaccine and wanted to register her son for the vaccine. The patient underwent lab tests and procedures which included blood pressure measurement: elevated. The events resulted in a visit to emergency room. The outcome of events unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683820
Sex: F
Age:
State:

Vax Date: 02/08/2021
Onset Date: 02/12/2021
Rec V Date: 09/08/2021
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: chills; fatigue; headache; This is a spontaneous report from a contactable other healthcare professional Nurse (patient). A female patient of age 66 (units not provided) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EM9809), via an unspecified route of administration on 08Feb2021 as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The caller stated she received the first dose of the vaccine late afternoon on 08Feb2021 and reported she had a reaction. She felt absolutely fine until 11Feb2021 when she went to bed and got chills. She never got a fever. On 12Feb2021 she had a bad headache and fatigue. She said the reaction was delayed and she felt fine for a couple days. She stated she woke up in the night between Thursday and Friday with chills but no fever. On Friday (12Feb2021) she had a headache, but it was manageable with Tylenol but then she had fatigue. She stated it all went away Saturday when she woke up like nothing happened, except for the intermittent headache that she managed with Tylenol. She said the headache was moderate and did not keep her down. She stated she had no respiratory issues. The caller asked if this was a reported reaction and if this may occur with the second dose. She heard the second dose had more symptoms. She was scheduled for the second dose on 01Mar2021. The patient took Tylenol for headache. All of the events subsided except the headache which was intermittent through the weekend but not bad. She could take Tylenol and it will go away. She wanted to make sure that these events are normal with the Pfizer COVID-19 Vaccine, as they started towards the very end of the anticipated timeline of side effect onset. She works as an HR Nurse and wanted to make sure it was ok to return to work. The outcome of all events was recovered except headache which was recovering. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1683821
Sex: F
Age:
State: OH

Vax Date: 02/06/2021
Onset Date: 02/15/2021
Rec V Date: 09/08/2021
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: Swelling and pain at injection site.; Swelling and pain at injection site.; This is a spontaneous report from a contactable consumer (patient). A 29-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EM9810), via an unspecified route of administration, administered in Arm Left on 06Feb2021 14:30 (at the age of 29-year-old) as dose 1, single for covid-19 immunisation. Medical history included hypothyroidism and allergy to adhesive in band aids. Concomitant medication(s) included spironolactone (ALDACTONE) taken for an unspecified indication, start and stop date were not reported, citalopram 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, retinol acetate (VITAMIN A) taken for an unspecified indication, start and stop date were not reported. Patient did not receive any other vaccine in four weeks. Other medications in two weeks included Aldactone, citalompram, levothyroxine, vit. A. The patient experienced swelling and pain at injection site on 15Feb2021 at 12:00AM. Symptoms started Monday the 15th, 10 days after the injection. Patient did not have covid prior vaccination and covid was not tested post vaccination. Patient did not receive treatment for adverse events. The outcome of swelling and pain at injection site was recovering. Follow-up attempts completed. No further information expected.

Other Meds: ALDACTONE [SPIRONOLACTONE]; CITALOPRAM; LEVOTHYROXINE; VITAMIN A [RETINOL ACETATE]

Current Illness:

ID: 1683822
Sex: F
Age:
State: TX

Vax Date: 02/04/2021
Onset Date: 02/10/2021
Rec V Date: 09/08/2021
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: throwing up all night, vomiting; massive headache; diarrhea; constipation problems; This is a spontaneous report from a contactable consumer (parent). A 33-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, batch/lot number: EN5318, Expiry Date: unknown), via an unknown route of administration on 04Feb2021 (at the age of 33-years-old) as DOSE 1, SINGLE for COVID-19 immunisation. The patients medical history was none. Concomitant medication was not reported. On 10Feb2021 (wednesday), the patient started having constipation problems, sometimes this happens, and she would take a stool softener or laxative and everything was fine. She did have little bit of diarrhea through the weekend but mainly the onset was on the 14Feb2021 but mainly right now she was throwing up on 15Feb2021. It was confirmed that patient received vaccine they were 11 days out and she had been throwing up since last night. She said medical information was not any help only had it happening about 7 days out. The vomiting and massive headache began 15Feb2021. She also had a massive headache that she started complaining about yesterday. The outcome of the event throwing up all night was not recovered. The outcome of the event constipation problems was recovered on an unknown date in 2021; while the outcome of the remaining events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683823
Sex: F
Age:
State:

Vax Date: 02/10/2021
Onset Date:
Rec V Date: 09/08/2021
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: nausea for a couple of minutes; felt sick; threw up flem; This is a spontaneous report from a contactable consumer (patient). A female patient of unspecified age received BNT162b2 (COMIRNATY, Formulation: solution for injection, Batch/lot number: not reported, Expiry date: Not reported), via an unspecified route of administration on 10Feb2021 as dose 1, single for COVID-19 immunisation. The patients medical history and concomitant medications were not reported. Patient had no known allergies. On an unspecified date, Patient was feeling nausea for a couple of minutes. She was sitting still and all of a sudden, she felt sick and she threw up flem. But after that, she was fine. The outcome of the events was recovered on an unspecified date. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683824
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/08/2021
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: This is a spontaneous report from a contactable consumer (patient). An 81-year-old female patient received unknown dose number of BNT162B2 (Pfizer-BioNTech COVID-19 vaccine, solution for injection, batch/lot# and expiration date not reported), via an unspecified route of administration, on an unspecified date, single dose, for COVID-19 immunisation. The patient's medical history and concomitant medications not reported. The patient experienced little sore on arm (a little blue and black) on an unspecified date. Caller would like to know if taking Tylenol was allowed after the Pfizer COVID-19 vaccine. Caller also wanted to know if experiencing no side effects after the 1st dose of the Pfizer COVID-19 vaccine means she will not have side effects after the 2nd dose as well. The outcome of event: unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1683825
Sex: M
Age:
State: MI

Vax Date: 02/15/2021
Onset Date: 02/16/2021
Rec V Date: 09/08/2021
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; headache; shivers; terrible muscles aches and pains; This is a spontaneous report from a contactable other HCP (patient). 38-years-old male patient received second dose of BNT162B2 (Pfizer-Biontech COVID-19 Vaccine, Solution for injection, batch/lot number: EL3248), via an unknown route of administration in left arm on 15Feb2021 at 09:00 (at the age of 38-years-old) as single for COVID-19 immunisation at clinic. The patient's medical history and known allergies were reported as none. Concomitant medication was not reported. No other vaccine in four weeks. The patient received first dose of BNT162B2 (Pfizer-Biontech COVID-19 Vaccine, Solution for injection, batch/lot number: EL3248), via an unknown route of administration in left arm on 25Jan2021 at 09:00 as single as historical vaccine for COVID-19 immunisation. On 16Feb2021 at 02:00, the patient woke up in middle of night with shivers. Had to get into shower just to keep warm. Muscles kept locking on whole body. Woke the next day with terrible muscles aches and pains. Along with great tiredness and headache. No COVID prior vaccination. No COVID tested post vaccination. No treatment received. The outcome of the event was not recovered. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1683826
Sex: M
Age:
State: WI

Vax Date: 02/15/2021
Onset Date: 02/15/2021
Rec V Date: 09/08/2021
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 Name: Covid tests; Test Result: Negative ; Comments: States he has had 12 in a row negative Covid tests.

Allergies:

Symptom List: Vomiting

Symptoms: large ringing in his right ear; This is a spontaneous report from a contactable consumer (patient). A 71-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL3248, Expiration Date: Apr2021), via an unspecified route of administration, administered in Arm Left on 15Feb2021 15:00 (at the age of 71-year-old) as dose 1, single for covid-19 immunisation at Hospital. Medical history included defibrillator was placed from Oct2020 to an unknown date (had a defibrillator so was seeing his Cardiologist and his heart was fine). Concomitant medication included on a series of holistic medication and prescribed medication. Other products were none. Additional vaccines administered on same date of the Pfizer suspect was reported as none. Prior Vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s) was reported as none. Family medical history relevant to event none. The caller reported that on 15Feb2021 18:00, he experienced large ringing in the right (R) ear and didn't know if this could be related. Caller stated that it has not gotten any better nor gotten any worse. He also stated he has had 12 in a row negative Covid tests. No emergency room/physician office visit. The patient underwent lab tests and procedures which included Covid tests: negative on an unspecified date (Stated he had 12 in a row negative Covid tests). Relevant tests none. Seriousness was reported as no by the reporter. The outcome of event was not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683827
Sex: F
Age:
State: VA

Vax Date:
Onset Date:
Rec V Date: 09/08/2021
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: Headaches; Feeling kind of sick; This is a spontaneous report from a Pfizer-sponsored program regulatory authority Support. A contactable consumer reported for a 6-decade-old female patient (reporter's daughter) who received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: Unknown), via an unspecified route of administration on an unspecified date in 2021 as SINGLE dose for covid-19 immunization. Historical vaccine included received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: Unknown), via an unspecified route of administration on 29Jan2021 as SINGLE dose for covid-19 immunization and experienced arm soreness. Medical history included breast cancer and had a lump and everything removed on an unknown date in 2013 and it was unknown if ongoing. Concomitant medication was not reported. The caller stated that her daughter experienced headaches and feeling kind of sick (caller stated that her daughter never gets sick, however immediately after she got a second Covid shot, she got headache). The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1683828
Sex: F
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 09/08/2021
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: Body ache; Feeling weak; This is a spontaneous report from a non-contactable consumer (patient). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number was not reported), via an unspecified route of administration, on an unspecified date, as dose 2, single, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received the second shot of the COVID-19 vaccine. The patient went to bed okay but woke up with body ache and feeling weak on an unspecified date, no fever. The patient asked what the company recommends for this. The outcome of the events was unknown. No follow-up attempts are possible; information about lot or batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1683829
Sex: F
Age:
State: MO

Vax Date: 02/13/2021
Onset Date: 02/15/2021
Rec V Date: 09/08/2021
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: Nauseous; had pains across my stomach/doubled up in pain; "I was sicker than a dog, throwing up, diarrhea (medicine which helped 'backed up' on me), and had sharp pains across my stomach".; This is a spontaneous report from a contactable consumer (patient). An 83-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number and Expiration date not reported), via an unspecified route of administration on 13Feb2021 as single dose for COVID-19 immunisation. Medical history included visual impairment from an unknown date and unknown if ongoing. The concomitant medications of patient were not reported. Caller reported that on Monday (15Feb2021) she was sicker than a dog, throwing up, diarrhea (medicine which helped backed up on her), and had sharp pains across her stomach. Consumer stated by Monday she started getting really sick and was doubled up in pain from everything. She reported she doesn't take a lot of medications they make her sick, she thought she was going to throw up or have diarrhea. She said that this morning (16Feb2021) she got up, she was very nauseous, more than usual, she took some pills for it, she did not have diarrhea, this was what she had going on and she was just really sick to her stomach and was right now too. She stated she had pains across her stomach that she had never had before, it was severe. The patient took some pills for nausea. The outcome of diarrhea was resolved, nausea and stomach pain were unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1683830
Sex: F
Age:
State: FL

Vax Date: 02/11/2021
Onset Date: 02/12/2021
Rec V Date: 09/08/2021
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: 20210205; Test Name: Investigation; Result Unstructured Data: Test Result:Unknown results; Comments: Lab test: Consumer stated, "Yes, it's a long result but yes, the date was 05Feb2021."

Allergies:

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

Symptoms: itching at the site of injection on her second dose; This is a spontaneous report from a contactable reporter (patient herself). The 85-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot Number: Unknown, Expiry Date: Unknown), dose 2 via an unspecified route of administration on 11Feb2021 (at the age of 85-years-old) as a DOSE 2, SINGLE for covid-19 immunisation. The patient medical history included hypertension (High blood pressure) from an unknown date and unknown if ongoing. Concomitant medication received were not specified. Reporter stated, I take lot of medications, hold on let me get my list of meds. I mean I had no problem; I was just aching with the first injection and I was alarmed when I started having itching with the second one. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot Number: not reported), dose 1 via an unspecified route of administration on 18Jan2021 (at the age of 85-years-old) as a DOSE 1, SINGLE for covid-19 immunisation. After first dose patient reported that, I mean I had no problem, I was just aching with the first injection and I have the first date, I have which was hold on, I don't know what, I guess. Reporter further stated, "I have the first date, I have which was hold on, I don't know what, I guess 18Jan2021. No, no, I mean anyone else reported the itching at the site." The patient experienced itching at the site of injection on her second dose on 12Feb2021. Reporter reported that she had a reaction of itching at the site of injection on her second dose of the Pfizer Covid vaccine dated 11Feb2021. She was asking if we have info same as this in our clinical trials. Reporter was asking for the efficacy of the vaccine as she has experienced some side effects after getting her second dose of the Pfizer Covid Vaccine. Reporter stated, "I just wanted to report that I got my second injection on last Thursday (11Feb2021) and starting Thursday evening for about I would say 2 or 3 days I had itching at the site of the injection, and I know that is not lot listed as one of the symptoms you have in your 23 pages of information." Reporter stated, "I called before even I got the first injection because I had so many questions that weren't answered for me." (Not clarified if called in Pfizer drug safety, hence case was marked as initial) Reporter stated, for facility name where the vaccine was administered that "It was continuing care residency, well they were issued by or distributed by pharmacy." Reporter further stated, "No, not really experiencing the event." Reporter stated, "Just what I want to know was the injection effective even though I had that itching, well I just have concern because I have long list of symptoms that you gave me, I mean the literature that I have and that was not one of them and I just wanted to be sure because it was different, you know and my results of receiving and having a medication effectiveness is not hampered." The patient underwent lab tests and procedures which included investigation for which results were unknown on 05Feb2021. Reporter stated, "Yes, it's a long result but yes, the date was 05Feb2021." Treatment was not received for the event. Outcome of the event was unknown. Information about lot and batch number was requested. Follow-up (13May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1683831
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/08/2021
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: Caller states they experienced a sore arm for a few days; slight pressure headache; This is a spontaneous report from a contactable nurse (patient). A 72-year-old female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as dose 2, single for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. Historical vaccine of BNT162B2 as dose 1, single for covid-19 immunisation was taken. The patient experienced a sore arm for a few days and slight pressure headache on an unspecified date. Outcome of the events was unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am