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: 1712321
Sex: U
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/18/2021
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: headache; my body was drained like really tired; slept all day; This is a spontaneous report from a non-contactable consumer communicated to Pfizer. This consumer reported. A patient with unspecified age and gender received a dose of BNT162B2 (BNT162B2, Formulation: Solution for injection, Lot Number: unknown, Expiration date: unknown), via unspecified route, administered on unspecified date as dose 2, single for COVID-19 immunization. Patient received a dose of BNT162B2 (BNT162B2, Formulation: Solution for injection, Lot Number: unknown, Expiration date: unknown), via unspecified route, administered on an unspecified date as dose 1, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date, after the vaccination, the patient experienced headache and her body was drained like tired. she didn't go to work Wednesday. The patient slept all day. On Thursday she felt much better and rested and went to work. The outcome of the events was recovering at the time of this report. No follow-up attempts possible. No further information expected.

Other Meds:

Current Illness:

ID: 1712322
Sex: F
Age:
State: FL

Vax Date: 02/23/2021
Onset Date: 02/24/2021
Rec V Date: 09/18/2021
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: Vomiting; Stomach ache; Fatigue extreme; Headache; Low grade fever; This is a spontaneous report from a contactable consumer (Patient). A 67-year-old female patient received first dose bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection Batch/Lot Number: EN6200), dose 1 via an unspecified route of administration on 23Feb2021 as dose 1, single for covid-19 immunisation. Medical history included immune thrombocytopenia from an unknown date and unknown if ongoing (Idiopathic thrombocytopenia). The patient's concomitant medications was not reported. On 24Feb2021 patient experienced extreme fatigue, headache, very low grade fever, vomiting, patient was feeling still fatigued but little headache just about it and patient question was though have Idiopathic thrombocytopenia and patient not known that should proceed with the second dose of vaccine or not. Patient received treatment with ibuprofen. The outcome of fatigue extreme and headache was not recovered and outcome of low grade fever, vomiting and stomach ache was unknown. No follow up attempts are possible. No further information is available.

Other Meds:

Current Illness:

ID: 1712323
Sex: F
Age:
State:

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

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

Lab Data:

Allergies:

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

Symptoms: flu; This is a spontaneous report from a Pfizer-sponsored program Covax US support. A Non contactable consumer reported for a female patient (reporter's sister). A female patient of unspecified age received a dose of BNT162B2 (BNT162B2, Formulation: Solution for injection, Lot Number: unknown, Expiration date: unknown), via unspecified route, administered on an unspecified route as dose 2, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date, after the vaccination, the patient got sick with the flu. The events assessed as non-serious. The outcome of the event was unknown. No follow-up attempts possible. No further information expected.

Other Meds:

Current Illness:

ID: 1712324
Sex: F
Age:
State: NY

Vax Date: 02/19/2021
Onset Date: 02/21/2021
Rec V Date: 09/18/2021
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: Rash is itching; rash trunk neck arm; This is a spontaneous report from a Contactable physician (Patient). A 56 year old female patient started to receive bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EL9269) via an unspecified route of administration on 19Feb2021 at as DOSE 1, SINGLE for COVID-19 immunization (at the age of 56 Years). Medical history included Benign essential tremor and Concomitant medication(s) included was on 20mg Propranolol and was switched to 60mg extended release for Benign essential tremor, which she had been on for a while now. Was switched at least a year ago. On 21Feb2021 The patient experienced rash started all over her body, neck, head, and arms. Rash is ongoing. Rash is itching. It was reported that, thought it would start to clear by now. Wanted to know if this is a normal response and should she take her second shot. Her breathing has not changed. She is just constantly itching and can't stop. Had been taking Hydrocortisone cream, Benadryl and also taking Pepcid, and Zyrtec for the H2 antihistamine. Zyrtec 10mg every night around 7PM Lot: 1797699 Exp: Jun2023, Pepcid: 10mg every night around 7PM Lot: SLF055 Exp: Aug2023 7PM, Benadryl: 25mg tablet at night, around 10PM, to go to sleep and stop itching. Lot: 16L0001 Exp: Jun2020, Clarified Hydrocortisone cream Cortisone 10 for eczema, itchy, dry skin, Exp: Aug2012, and she is applied as many times as she can and also reported taking benadryl and hydrocortisone cream for the itching. It still itching non-stop. She noticed it is expired when looking for the expiry. Stated that is maybe why it is not working. Outcome of the event was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds: PROPRANOLOL

Current Illness:

ID: 1712325
Sex: M
Age:
State: MD

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

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

Lab Data: Test Date: 20210226; Test Name: nasal Swab; Result Unstructured Data: Test Result: Unknown Result; Comments: result: Pending.

Allergies:

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

Symptoms: injection site pain; arm soreness; muscle aches; pains in forearms,shoulders, abdomen, quadriceps, and calves.; minor joint pain; swollen lymph nodes under both arms.; fatigue; exercise intolerance; This is a spontaneous report from a contactable physician. A 29-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number: EL9264, Expiration Date: not reported) via intramuscular, administered in left arm on an unspecified date as dose 2, single for COVID-19 immunization at the age of 29-year-old. Patient previously took BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number: EN5318, Expiration Date: not reported) via intramuscular, administered in left arm on 29Jan2021 as dose 1, single for COVID-19 immunization. Medical history included known allergies to tree nuts, shell fish, penicillin. Patient had covid-19 prior vaccination. The patient's concomitant medications were not reported. Patient did not receive other vaccine in four weeks. The patient experienced some injection site pain and arm soreness, patient had no side effects for the first day. Two days after vaccinated, started debilitating muscle aches and pains in forearms, shoulders, abdomen, quadriceps, and calves. Also had some minor joint pain and swollen lymph nodes under both arms, patient noted fatigue and exercise intolerance since injection on an unspecified date. Resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. The patient was covid tested post vaccination. The patient underwent lab tests and procedures which included sars-cov-1 test (Nasal Swab) unknown on 26Feb2021, result was pending. Patient did not receive treatment for the events. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1712326
Sex: F
Age:
State:

Vax Date: 02/25/2021
Onset Date:
Rec V Date: 09/18/2021
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: almost fainted; dizzy; was also very shaky; her heart beating really fast; having other symptoms that she don't know if they may be an allergic reaction; This is a spontaneous report from a contactable consumer (Patient herself). A 42 (unspecified unit) old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection) via an unspecified route of administration on 25Feb2021 (Batch/Lot number was not reported) as DOSE 2, SINGLE for covid-19 immunisation. The patient's medical history was not reported. The patient's concomitant medications were not reported. Patient stated that she received her second COVID-19 vaccine and experienced some other side effects. she does have some medication allergies and allergic to one of the vaccines. After 1 hour of taking the vaccine she was dizzy and almost fainted twice; again after one and half hour later of taking the vaccine she got really dizzy. It happened 2 times right after the vaccine. She said she was also very shaky and her heart beating really fast, now as well. Patient wanted to know if they were allergic reactions. Reporter said she got the second dose of the vaccine yesterday. Outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1712327
Sex: F
Age:
State: KY

Vax Date: 02/23/2021
Onset Date: 02/26/2021
Rec V Date: 09/18/2021
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: fever; Result Unstructured Data: Test Result:99.9

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: chills; didn't sleep good last night; sore shoulder; Achy; flu like symptoms; muscle aches; fever; little bit of a headache; This is a spontaneous report from a contactable consumer or other non-hcp (Patient). A 69-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection; Lot Number: EN8202; Expiration Date: 30Jun2021) via an unspecified route of administration (age at vaccination 69-year) in arm left on 23Feb2021 as dose 1, 0.3 ml single for COVID-19 immunization. Medical history reported none. There were no concomitant medications. On 26Feb2021 the patient experienced flu like symptoms, muscle aches, fever, little bit of a headache, didn't sleep good last night, achy; on an unspecified date the patient experienced sore shoulder, chills, and didn't sleep good last night. The patient underwent lab tests and procedures which included body temperature: 99.9 on an unspecified date. As reported "the symptoms started this morning when the patient woke up, she didn't sleep good last night, she has a sore shoulder. When the patient got up, she had these other symptoms. The patient has taken some Tylenol, but the Tylenol hasn't had time to kick in. Question asked by the patient if she could get her second dose of the vaccine given that she had these side effects post vaccination. She was scheduled to receive the second dose of the vaccine 3 weeks after dose 1. If she wants to change her appointment date how far she could extend it." Therapeutic measures were taken as a result of sore shoulder, the patient was treated with Tylenol. The clinical outcome of the event flu like symptoms, muscle aches, fever, achy, was not resolved; outcome of little bit of a headache was resolving; while the outcome of other events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1712328
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/18/2021
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: arm is slightly itchy and scratching; there's a pinkish area approximately an inch in diameter; This is a spontaneous report from a contactable consumer or other non hcp. This (Age:90; unit: Unknown) female consumer reported that the patient received the bnt162b2 ((PFIZER-BIONTECH COVID -19 VACCINE, Injection for injection, dose 1 at an unspecified date (Batch/Lot number was not reported, expiry date: unknown) as SINGLE DOSE for covid-19 immunization on Wednesday (age at vaccination: 90 (unit not specified)). The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced arm is slightly itchy and scratching (pruritus) on an unspecified date, there's a pinkish area approximately an inch in diameter (erythema) on an unspecified date. The outcome of all events was reported as unknown. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1712329
Sex: F
Age:
State:

Vax Date: 02/03/2021
Onset Date:
Rec V Date: 09/18/2021
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: skin crawling feeling; joint stiffness; itchy rash on leg and skin crawling and itchiness for the next 24 hours; myaelgia; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received first dose of bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, batch/lot number: EL9265, expiration date: not reported) via an unspecified route of administration on 03Feb2021 as DOSE 1, SINGLE for COVID-19 immunisation. Consumer stated, "I needed to talk to a medical professional at Pfizer. I am of age 60 (not clarified), I have had the first Covid vaccine. I do have rheumatoid arthritis and long history of allergies to many things. So, I do have like immune problems to begin with. The patient's concomitant medications were not reported. But, not immediately, not within the first 30 minutes, but I had it in first hour or hour and a half, after my first shot, I got a small rash on my leg probably like four inches in diameter, it itched. So, I put some prescription strength Cortisone cream on it and it went away. But then for the next 24 hours, I did not have any like I would say rash but I had severe skin itching like skin crawling feeling. So, what I need to know was, I am looking at the CDC guidelines for what you guys classify an allergic reaction and there was a start of a grey area. It was reported that the patient experienced skin crawling feeling, itchy rash on leg and skin crawling and itchiness for the next 24 hours, myalgia, joint stiffness on an unspecified date. The outcome of the events was unknown. No follow-up attempts are possible. No further information was expected.

Other Meds:

Current Illness:

ID: 1712330
Sex: F
Age:
State: SC

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 09/18/2021
Hospital:

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

Lab Data: Test Name: Body temperature; Result Unstructured Data: Test Result: 99.8 Fahrenheit; Test Name: Body temperature; Result Unstructured Data: Test Result: 88.8 Fahrenheit.

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: feels rotten/feeling so rotten; running a temperature; both arms are hurting; headache; so tired; diarrhea; loss of appetite; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 75-Year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN9581, Expiry date, NDC number: unknown) via an unspecified route of administration, administered in left arm on 25Feb2021 (age at vaccination was 75 years) as dose 2, single for COVID-19 immunisation. The patient medical history includes congestive heart failure on an unspecified date in Aug2018, unknown and unknown if ongoing and rheumatoid arthritis, diagnosed 10 years; both were from an unknown date and unknown if ongoing. Concomitant medications were not reported. Historical vaccine includes first dose of BNT162B2 (Lot Number: unknown) in left arm on 04Feb2021 (age at vaccination was 75 years) for COVID-19 immunisation. On 25Feb2021, the patient was feeling so rotten this morning and was running a temperature, wants to know could this be normal, states patient was miserable last night, that the injection was in the left arm and both arms was hurting, states patient couldn't sleep on either side and developed a headache, her temperature this morning around 9 AM 99.8 degrees F. Also feels so tired and experienced loss of appetite. Had some diarrhea last night before bed, not bothering her this morning. The patient treated her symptoms with Tylenol, that her temperature went from 99.8 degrees to 88.8 degrees F after the Tylenol. The patient was asking are these are common side effects. No investigation assessment. Outcome of the event diarrhea was resolving, events feels rotten/feeling so rotten and loss of appetite were unknown and remaining events were not resolved. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1712331
Sex: F
Age:
State: OK

Vax Date: 02/20/2021
Onset Date: 02/21/2021
Rec V Date: 09/18/2021
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: Rash all over the body - chest, abdomen, breast, upper legs and arms, shoulders; Itching; Chills; Fever; Nausea; This is a spontaneous report from a contactable nurse (patient). A 73-years-old female patient received second dose of bnt162b2 (BNT162B2, solution for injection), via an unspecified route of administration, administered in arm left on 20Feb2021 16:00 (Batch/Lot number was not reported) (at the age of 73-years-old) as SINGLE for covid-19 immunization. Historical vaccine included received first dose of bnt162b2 (BNT162B2, solution for injection), via an unspecified route of administration, administered in arm left on 23Jan2021 on an unspecified time (Batch/Lot number: E79231) (at the age of 72-years-old) as SINGLE for covid-19 immunization. Patient Medical history included pituitary problems, she had a tumor twice and had radiation and surgery from an unknown date and unknown if ongoing. The patient mentioned a previous reaction to a tetanus vaccine, it had to have been a DPT, when she was a baby. The patient's doctor told her mother to never get her another one. The patient does not have the lot number or expiration for it. Patient denied for any concomitant medications. It was reported that patient had the second dose of the Pfizer Covid vaccine and on the 20th, on the Tuesday after that she started getting a rash over quite a bit of her body and is still there. The patient mentioned the paperwork said that a bad rash all over the body could mean a severe allergic reaction but she has had no difficulty breathing, no swelling of the face, tongue and throat, and no fast heartbeat. On 20Feb2021 4:00, The patient received the shot and by 4:00 in the morning of 21Feb2021 she started getting chills, fever, and nausea. All of those symptoms may have lasted 24 hours, but the patient is not having those symptoms anymore, it is just the rash that is bothering her. The patient knows that the rash was there on Tuesday but it could have been Monday when she had some itching, but she did not look at that time. The patient wanted to knew if she should worry about this and how long would the rash last. The outcome of events for chills, fever, and nausea was recovered on an unspecified date in Feb2021 whereas for Itching it was unknown and for rash all over the body chest, abdomen, breast, upper legs and arms, shoulders outcome of events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1712332
Sex: F
Age:
State: VA

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 09/18/2021
Hospital:

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

Lab Data: Test Date: 20210215; Test Name: Sars-COV-2; Test Result: Positive

Allergies:

Symptom List: Rash, Urticaria

Symptoms: weak feeling; joints are also a little achy today.; a little achy as well; a little bit of a drippy nose; felt weird in her arm as she got the injection; face is flushed; sore arm; chills; This is a spontaneous report from a contactable consumer (patient) other non-healthcare professional. A 68-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EN6198; Expiry date: 30Jun2021) via an unspecified route of administration, on 25Feb2021, in left arm, as dose 1, single (at the age of 68 year) for covid-19 immunisation. Medical history included covid-19 from 12Feb2021 to an unknown date, headache from Feb2021 to an unknown date, she only had mild symptoms like a headache, Rhinorrhoea from 12Feb2021 to an unknown date, blood pressure and an allergy medicine. Concomitant medications were not reported. On 25Feb2021 the patient experienced sore arm, Chills, face is flushed and from an unspecified date patient had weak feeling, joints are also a little achy today, felt weird in her arm as she got the injection, little achy as well, a little bit of a drippy nose. On 15Feb2021 the patient underwent lab tests and procedures which included sars-cov-2 test: positive. Treatment was taken for face is flushed with Ibuprofen. Patient was asking that what's Pfizer statement regarding researchers saying Pfizer-BioNTech COVID-19 Vaccine's second dose can be delayed as first dose is highly effective. The clinical outcome of all events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1712333
Sex: F
Age:
State: NY

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 09/18/2021
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: burning eyes; fever; headache; lighthead; nausea; strong pain in the arm; This is a spontaneous report from a contactable consumer or other non-healthcare professional. A 46- year-old non-pregnant female patient (not pregnant at the time of vaccination) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/lot number was not reported) via an unspecified route of administration on 25Feb2021 at 04:30 PM (46-year-old at the time of vaccination) at a dose number unknown, single for covid-19 immunization. The patient medical history was not reported. The patient previously took Amoxicillin (AMOXICILLIN) and experienced allergies. The patient's concomitant medications were not reported. The patient had not received any vaccine within four weeks. The patient had no covid prior to vaccination. The patient was not tested since vaccination. On 25Feb2021 06:00 PM, the patient experienced fever, headache, light head, burning eyes, nausea and strong pain in the arm. No treatment received for the events. The outcome of the events were recovering. Information about lot/batch number has been requested. Follow-up: Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1712334
Sex: M
Age:
State:

Vax Date: 01/28/2021
Onset Date:
Rec V Date: 09/18/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: sick; This is a spontaneous report from a contactable consumer or other non-HCP (patient wife) via Pfizer-sponsored program. A male patient of an unspecified age received BNT162b2 (PFIZER BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- UNKNOWN) via an unspecified route of administration on 28Jan2021 as dose 1, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced sick (reported as he has to go to the hospital) on an unspecified date. He got his 1st dose on 28Jan2021. She wants to know if he will now have to revaccinate since he was going to miss the 2nd dose. The outcome of the event was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1712335
Sex: M
Age:
State: GA

Vax Date: 02/19/2021
Onset Date: 02/01/2021
Rec V Date: 09/18/2021
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: This is a spontaneous report from a contactable consumer (patient's spouse). An 80-year-old male patient (husband) received the first dose of BNT162B2 (PFIZER BIONTECH COVID-19 VACCINE) via an unspecified route of administration, administered in left arm on 19Feb2021 (batch/lot number: EN9581) at 80 years old, as SINGLE DOSE for COVID-19 immunization (also reported as "because of the age, he didn't want to get COVID"). The patient's medical history included ongoing blood pressure high diagnosed years ago; cholesterol (blood cholesterol abnormal) from an unknown date; and leg amputation on an unknown date in 2020, reported as "one year ago." Concomitant medications included atorvastatin (ATORVASTATIN) taken for blood cholesterol (blood cholesterol abnormal) from an unspecified start date and ongoing; acetylsalicylic acid (ASPIRIN) taken for a long time, carvedilol (CARVEDILOL), clopidogrel (CLOPIDOGREL), fenofibrate (FENOFIBRATE),isosorbide (ISOSORBIDE), lisinopril (LISINOPRIL), and spironolactone (SPIRONOLACTONE), all taken for an unspecified indication, from an unspecified start date and ongoing. It was reported that the patient took the Pfizer shot (clarified as Covid vaccine) on Friday, 19Feb2021 and then, that night, he broke out a little rash. The reporter gave the patient some Benadryl 25mg tablet and it cleared up and went away. On 20Feb2021, Saturday, patient felt okay. Then, Sunday (21Feb2021) this morning he woke up and was nauseous/ feeling nausea. He has been having nausea all day on Sunday. He had been throwing up on and off all day. The reporter gave the patient a nausea pill (unspecified medication), Ginger ale (also reported as "Gingerol"), and crackers but it kept coming, his stomach was not settled. The reporter asked, "what should I do?" He has stopped the throwing up, but the reporter wanted to know what else they can do to get him back up to speed. It was further reported that the patient was queasy and doesn't really have an appetite since an unspecified date in Feb2021. The reporter had been giving him fluids and they all stayed down, and he has not had an episode since Sunday. But he still feels weak after throwing up all day. So, the reporter asked, "was there anything special I need to do?" The patient stopped throwing up and nausea, but he still doesn't feel good. Then reporter stated that the patient still had nausea, but he was not throwing up, it stopped yesterday on 22Feb2021. Nausea is about the same. Rashes stopped. When he threw up all day Sunday, he has been drinking water and liquids. Therapeutic measures were taken as a result of the events rash, nauseous/ feeling nausea/ stomach was not settled/ queasy, and throwing up. The patient recovered from the event rash on an unspecified date in Feb2021 and recovered from the event throwing up on 22Feb2021; has not recovered from the event nauseous/ feeling nausea/ stomach was not settled/ queasy. Outcome of the other events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: ATORVASTATIN; ASPIRIN [ACETYLSALICYLIC ACID]; CARVEDILOL; CLOPIDOGREL; FENOFIBRATE; ISOSORBIDE; LISINOPRIL; SPIRONOLACTONE

Current Illness: Blood pressure high (diagnosed years ago)

ID: 1712336
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 09/18/2021
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: Her sister reported that on the 5th day she got a tremendous pain in her arm where she got the Pfizer COVID-19 Vaccine shot; Is almost like the flesh is being sucked underneath the titanium plate, there is like no blood or anything but there is a hole; This is a spontaneous report from a contactable consumer. This is report 2 of 2. A female patient of an unspecified age received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported, Expiry date: unknown), via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. Her sister reported that on the 5th day, the patient experienced a tremendous pain in her arm where she got the Pfizer covid-19 vaccine shot, was almost like the flesh was being sucked underneath the titanium plate, there was like no blood or anything but there was a hole on an unspecified date. The outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1712337
Sex: F
Age:
State: IL

Vax Date: 02/18/2021
Onset Date: 02/01/2021
Rec V Date: 09/18/2021
Hospital:

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

Lab Data: Test Date: 202102; Test Name: feverish; Result Unstructured Data: Test Result:little elevated; Test Name: A1C; Result Unstructured Data: Test Result:in the fives; Comments: numbers have been pretty good. A1C is in the fives; Test Name: Weight; Result Unstructured Data: Test Result:about 160 lbs

Allergies:

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

Symptoms: body aches; hips were hurting; lost the sense of smell; pressure behind her eyes; stuffy nose; Headache; sore arm; felt a little feverish/It was a little elevated; feel as bad as she did; This is a spontaneous report from a contactable consumer (patient) via Medical information team. A 57-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EN6200), via an unspecified route of administration, administered in Arm Left on 18Feb2021 16:00 (age at the vaccination 57-year-old) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included type 2 diabetes mellitus from Jul2020 to an unknown date and high blood pressure. Concomitant medications included metformin and metoprolol for high blood pressure. Patient had the Pfizer shot on 18Feb2021 which was last Thursday. The next day, 19Feb2021, she had a sore arm. Since patient developed stuffy nose and headache on 21Feb2021, body aches on 25Feb2021, lost sense of smell on 24Feb2021, patient also had pressure behind the eyes on 23Feb2021, patient felt a little feverish, but it did not register as a fever on an unspecified date in Feb2021. It was a little elevated. on day seven she had body aches. Specifically, both hips were hurting on 25Feb2021 It was achy like she had stretched too much. Today she feels a little better. Patient still has stuffiness, body aches, and still cannot smell. She does not feel as bad as she did on an unspecified date in Feb2021. Therapeutic measures were taken as a result of all events. The patient underwent lab tests and procedures which included feverish: little elevated on Feb2021, glycosylated haemoglobin (A1C): in the fives (numbers have been pretty good. A1C is in the fives), weight: about 160 lbs on an unspecified date. The outcome of the events stuffy nose, lost the sense of smell, body aches were not recovered, hips were hurting and feel as bad as she did was recovering and unknown for another events. No follow-up attempts are possible. No further information is expected.

Other Meds: METFORMIN; METOPROLOL

Current Illness:

ID: 1712338
Sex: F
Age:
State: CT

Vax Date: 02/24/2021
Onset Date: 02/24/2021
Rec V Date: 09/18/2021
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: slight wheeze; Neck stiffness; temperature of 100; chest tightness; Moderate muscle/body aches; Moderate muscle/body aches; fever developed overnight and persistent through the day on 25Feb (with high temp of 101.5 25Feb evening).; armpit pain.; Sore arm started evening of 24Feb21.; This is a spontaneous report from a contactable consumer (patient). A 53-years-old non- pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Batch/Lot Number: EL3247), dose 2 via an unspecified route of administration, administered in Arm Right on 24Feb2021 11:45 (at the age of: 53-years-old) as dose 2, single for covid-19 immunisation. Patient was not pregnant at the time of vaccination. Medical history included hypertension, blood cholesterol, overweight, Allergy to Penicillin, mushrooms. Concomitant medications included metoprolol, lisinopril and atorvastatin taken for an unspecified indication, start and stop date were not reported. Historical vaccine of BNT162B2 for COVID-19 immunization on 04Feb2021 at the age of 52 year. Prior to vaccination patient was not diagnosed with covid 19. Patient did not receive any other vaccine prior to four weeks of covid vaccination, not tested for covid since the vaccination, patient reported that she was allergic to penicillin and mushrooms. On 24Feb2021 patient experienced sore arm, moderate muscle and body pain, fever developed overnight and persistent through the day on 25feb2021, chest tightness, slight wheeze, neck stiffness and armpit pain on an unspecified date. 26Feb21 am temperature of 100, body aches starting to ease. The outcome of sore arm moderate muscle and body aches and fever was recovering. No follow-up attempts are needed. No further information is expected.

Other Meds: METOPROLOL; LISINOPRIL; ATORVASTATIN

Current Illness:

ID: 1712339
Sex: F
Age:
State: NM

Vax Date: 02/25/2021
Onset Date: 02/26/2021
Rec V Date: 09/18/2021
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: quarter sized blister on right thigh; her leg started itching; It is not red, but kind of stings; burning just caught her attention; This is the spontaneous report from a contactable other health care professional (Nurse), reporting for herself. A 75-years-old female received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection; Batch no: not reported, Lot Number: EL9269; expiration date: unknown) via an unknown route of administration, administered in left arm on 25Feb2021 (at the age of 75-years-old) as dose 2, single for covid-19 immunization. Patient medical history included Kidney stones, below normal kidney function and thyroid disease and concomitant medications were not reported. The patient historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch no: not reported /Lot Number: EL9269, expiration date: unknown) administered via unknown route on 04Feb2021 as dose 1, single for COVID-19 immunization. Patient stated that she had the second COVID vaccine on 25Feb2021 and on 26Feb2021, patient experienced quarter sized blister on her right thigh, when she woke up in morning. It was not red, but kind of stings. With the second COVID Vaccine there really was no problem and had no pain after the injection. But her leg started itching and noticed the big size blister. Seriousness was reported as not life threatening but the burning just caught her attention. Patient was asking could that be a reaction from the COVID Vaccine. Investigation Assessment was reported as No. Treatment included with cleaned out the blister and applied Neosporin. The outcome of the events is unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1712340
Sex: F
Age:
State: AR

Vax Date: 02/04/2021
Onset Date: 02/01/2021
Rec V Date: 09/18/2021
Hospital:

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

Lab Data: Test Name: Lab work; Result Unstructured Data: Test Result:unknown results

Allergies:

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

Symptoms: Tightness in chest; my throat did get tight feeling; Dizziness; I had feverish red places going all the way down to my arm to my fingers; rashy stuff on my fingers and my whole hand and arm went numb.; rashy stuff on my fingers and my whole hand and arm went numb.; Rosacea on my face; Face was very itchy; I could feel the lymph nodes behind my right ear; This is a spontaneous report from a contactable consumer (patient). A 52-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EM9809), via an unspecified route of administration, administered in right arm on 25Feb2021 (at the age of 52-year-old) as dose 2, single for COVID-19 immunization; diphenhydramine hydrochloride (BENADRYL), via an unspecified route of administration from an unspecified date (Batch/Lot number was not reported) to an unspecified date, at 50 mg for an unspecified indication; paracetamol (TYLENOL), via an unspecified route of administration from an unspecified date (Batch/Lot number was not reported) to an unspecified date, at 2000 mg for an unspecified indication. Medical history included diabetes, Allergies: mold, yeast, beef, 17 kinds of trees and 4 major grasses that get used, anything that is fermented. Concomitant medications included insulin lispro (INSULIN LISPRO) taken for diabetes mellitus, start and stop date were not reported; insulin glargine (TOUJEO) taken for diabetes mellitus, start and stop date were not reported, Metformin XR taken for diabetes mellitus, start and stop date were not reported. The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EN5318), on 04Feb2021 (at the age of 52-year-old) as dose 1, single for covid-19 immunization and had a moderate to severe reaction, and previously took ozempic and experienced drug hypersensitivity. Patient HCP advised her to pre-treat with 50mg of benadryl and 2000mg of Tylenol before receiving her second dose yesterday at around 10:30. On an unknown date after second vaccination, the patient experienced tightness in chest, my throat did get tight feeling, dizziness, feverish red places going all the way down to arm to fingers, rashy stuff on fingers and whole hand and arm went numb, rosacea on my face, face was very itchy. Patient waits at the vaccination site for 30 minutes and reports dizziness and tightness in her chest and she could not tell if it was her heart or her bronchiole tubes. Since she is a teacher, she returned to work. While at work 14:30-15:00 she said, Her right arm (that she got the shot in) felt feverish and started having redness that extended down her arm, rashiness, all the way down to right pointer finger, and whole arm and hand were periodically going numb. The patient went to urgent care, where they advised her not to have any additional "booster" shots should they be deemed advisable in the future. Patient experienced rosacea on her face and her face was very itchy and her throat did get tight feeling, but it did not close, and she could feel the lymph nodes behind her right ear (incomplete sentence). Seriousness of the events was reported as non-serious. Patient wanted to know exactly which ingredients in the vaccine had for which she was having an allergic response to. Patient gave herself the Insulin shot, it was like fire ant biting on the inside of my arm. (Insulin details was not clarified further). Patient underwent unspecified lab tests with unknown test results on an unspecified date. The patient took Benadryl and Tylenol before she had the second shot of vaccine about an hour and a half before. Consumer stated that her allergy medicines, include Xyzal, Benadryl and Cetirizine (Did not clarify further). The outcome of events was unknown. No follow-up attempts are possible. No further information is expected.

Other Meds: INSULIN LISPRO; TOUJEO; METFORMIN XR

Current Illness:

ID: 1712341
Sex: F
Age:
State: NM

Vax Date: 02/10/2021
Onset Date: 02/10/2021
Rec V Date: 09/18/2021
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: itching to arms and face, progressing to the Bilateral arms and back/ residual itching; This is a spontaneous report from a contactable Pharmacist. This Pharmacist reported for a female patient. A 53-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection, Lot Number: EN6201), via intramuscularly, on 10Feb2021 09:30 AM (at the age of 53-year-old) as a dose 2, single for COVID-19 immunization. The patient medical history included allergies to NKDA food, shellfish, shrimp, citrus, poultry, nuts, mushrooms and other medical history HTN (hypertension), anxiety and hypothyroidism. Patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: unknown), via unspecified route of administration on unspecified date as a dose 1, single for COVID-19 immunziation. The concomitant medication of the patient included levothyroxine sodium (LEVOTHYROXINE SODIUM) and bupropion hydrochloride (WELLBUTRIN). It was unknown if patient had taken other vaccine in four weeks and it was unknown if patient had COVID prior vaccination. It was unknown if patient tested post COVID vaccination. On 10Feb2021 10:15 approximately 10 minutes after vaccine the patient experienced itching to arms and face, progressing to the bilateral arms and back. Patient was taken to the first aid station and denies any SOB, swelling, no CP and patient was A & O x 3, VSS at blood pressure was 1238/76, heart rate was 76, RR 18, SaO2 at 95% on RA. On 10:25 AM patient Itching had improved with blood pressure of 126/68, heart rate of 80, RR 16, SaO2:96% on RA. On 10:45 itching improved but residual itching continues. Patient was observed for 45 minutes and discharged. Patient received the treatment of Benadryl 25mg Oral liquid. Patient communicated understanding and had no further question prior to discharge. The outcome of the event was recovered on unspecified date in 2021. Follow-up attempts completed. No further information expected.

Other Meds: Levothyroxine Sodium; WELLBUTRIN

Current Illness:

ID: 1712342
Sex: F
Age:
State: NY

Vax Date: 01/21/2021
Onset Date:
Rec V Date: 09/18/2021
Hospital:

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

Lab Data: Test Name: colonoscopy; Result Unstructured Data: Test Result:had no reaction; Test Name: covid-19; Test Result: Negative ; Test Name: Weight; Result Unstructured Data: Test Result:20 lbs; Comments: gained

Allergies:

Symptom List: Unevaluable event

Symptoms: rash; soreness in her arm /Pain in lower part of her arm, below elbow; Headache; Arm tender to touch; This is a spontaneous report from a contactable consumer or other non-Health Care Professional. A 74-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EL3247 and Expiry date: Unknown), via an dose 1 intramuscular, administered in Arm Left on 21Jan2021 as DOSE 1, SINGLE for Covid-19 immunization. Medical history included allergy to chemicals, allergy to synthetic fabric from an unknown date and unknown if ongoing polyester thread causes a rash , allergy to vaccine, bronchiectasis from an unknown date and unknown if ongoing Diagnosed in the early 90's. She guesses this is in her bronchial tubes. She has green mucus every day. /takes 1600 mg guaifenesin for bronchiectasis, , ongoing atypical mycobacterial infection Diagnosed in the early 90's. She explains this is in her right lung, either her lower lobe or middle lobe, she is not sure. She was told this never goes away , pneumonia from an unknown date and unknown if ongoing 150 mg of some type of penicillin on Mondays, Wednesdays, and Fridays. The patient's concomitant medications were not reported. The patient previously took pneumococcal vaccine for immunization, varicella zoster vaccine for immunization and experienced pain in extremity, azithromycin and experienced drug hypersensitivity, levaquin and experienced drug hypersensitivity. On an unspecified date the patient experienced rash, soreness in her arm /pain in lower part of her arm, below elbow, headache, arm tender to touch. She had pain for almost 2 weeks in the lower part of her arm .The patient underwent lab tests and procedures which included colonoscopy had no reaction on an unspecified date, sars-cov-2 test: negative on an unspecified date, weight: 20 lbs on gained. The outcome of event was unknown. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness: Atypical mycobacteriosis (Diagnosed in the early 90's. She explains this is in her right lung, either her lower lobe or middle lobe, she is not sure. She was told this never goes away.)

ID: 1712343
Sex: F
Age:
State: VA

Vax Date: 02/05/2021
Onset Date: 02/12/2021
Rec V Date: 09/18/2021
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: Test Name: MRI; Result Unstructured Data: Test Result:degenerated disc from L5-sacrum; Comments: She had an MRI on the back, this was prior to the first dose a long time ago, the result was a degenerated disc from L5-sacrum.; Test Date: 20210219; Test Name: Covid Rapid Test/ covid test; Test Result: Negative

Allergies:

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

Symptoms: Diarrhea; Tightness in chest; Sinus congestion; scratchy throat; Nausea; Itchy eyes; Swollen lymph nodes; severe headaches; light sensitivity; ears hurting; huge bump behind the ear; Condition worsened/these symptoms have progressed as days went on; This is a spontaneous report from a contactable Consumer (patient). A 35-years-old female patient received BNT162B2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EM9809) via an unspecified route of administration, administered in arm left on 05Feb2021 11:30 (at early noon) as dose 1, single (age at vaccination 35 years) for COVID-19 immunization. The patient's Medical history was not reported. There were no concomitant medications. The patient experienced swollen lymph nodes, headache on 12Feb2021, sinus congestion, scratchy throat on 19Feb2021, itchy eyes on 17Feb2021, tightness in chest on 22Feb2021, nausea on 18Feb2021, diarrhea on 26Feb2021, huge bump behind the ear on an unknown date in 2021, on an unknown date in 2021 condition worsened/these symptoms have progressed as days went on, light sensitivity, ears hurting on 12Feb2021. The patient underwent lab tests and procedures which included magnetic resonance imaging (MRI): degenerated disc from l5-sacrum, she had an MRI on the back, this was prior to the first dose a long time ago, the result was a degenerated disc from L5-sacrum on an unknown date, Covid Rapid Test/ covid test on 19Feb2021 with negative result. Patient saw her doctor and had a covid test in which it came back negative, doctor told her it was probably just a virus of some sort and recommended to receive the second dose as long as she did not have a fever, patient does not have a fever, but the symptoms progressively have gotten worse. Patient's second appointment was scheduled but stated that she did not receive it due to her symptoms, it was also reported as around the 10Feb, 11Feb or 12Feb she began developing symptoms she has swollen lymph nodes and headache. She has had a headache every day since 11th or 12th. She is 35, and a healthy PE teacher. She experienced light sensitive sinus congestion, scratchy throat. She has an upcoming second shot today, but she has not gotten it. She figured to get tested for covid, last Friday she got a covid test, she did 2 types of tests one was a Rapid test and the second was a Long term one in which they give results 2-3 days later, the result of both tests were negative. She just started taking an antihistamines like cetirizine. She was also taking sudafed and mucinex, the doctor told her it may be a virus of some sort. With her throat congestion she has never felt pressure nasally and no stuffy nose, but she feels it in the throat in last 2-3 days. Her chest is tighter and this morning it progressed into diarrhea and nausea. Caller states that she was supposed to get second shot today but a couple nurses have advised to not get it yet, maybe the body thinks it has covid, Headache: Started on 12Feb2021, its ongoing, since it has started she has not had a day without it, it was progressively getting worse, sinus congestion: started on 19Feb2021, ongoing worsened, scratchy throat: Started on 19Feb2021, ongoing worsened, itchy Eyes: started on 17Feb2021, it is not as bad but ongoing, she squeezes her eyes she has contacts she wears, her eyes are just swollen, it is persisting, patient she has not had a fever at all. Patient had an MRI on the back, this was prior to the first dose a long time ago, the result was a degenerated disc from L5-sacrum. She does not think this is related. The outcome of the events diarrhea, huge bump behind the ear, Condition worsened/these symptoms have progressed as days went on, light sensitivity and ears hurting was unknown, Swollen lymph nodes was recovering, other events was not resolved. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1712344
Sex: F
Age:
State: CA

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 09/18/2021
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: taste in her throat; bad headache; pins and needles sensation on the lower portion of her face and tongue; Itchy; This is a spontaneous report from a contactable consumer (patient). A 68-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection,Batch/Lot Number: EN6198,Expiry date was not reported), dose 1 via an unspecified route of administration, administered in Arm Right on 25Feb2021 16:15 as 1ST DOSE, SINGLE for covid-19 immunisation,(Age at vaccination-68 years). Medical history included ongoing food allergy, ongoing drug hypersensitivity(Does not do well with Penicillin or Sulfa), blood pressure abnormal, thyroid atrophy,drug hypersensitivity (Does not do well with Penicillin or Sulfa) from an unknown date and unknown if ongoing. Concomitant medication(s) included levothyroxine sodium (TIROSINT) taken for an Thyroid, amlodipine taken for an blood pressure, zolpidem tartrate (AMBIEN) taken for an sleep ,unspecified start date and ongoing. On 25Feb2021 The patient experienced taste in her throat, bad headache, pins and needles sensation on the lower portion of her face and tongue, itchy. The patient had not received any other vaccine within 4 weeks. The patient visited emergency room/ physicians office. The clinical outcome was recovered. No follow-up attempts are needed. No further information is expected.

Other Meds: TIROSINT; AMLODIPINE; AMBIEN

Current Illness: Penicillin allergy; Shellfish allergy

ID: 1712345
Sex: F
Age:
State:

Vax Date: 02/08/2021
Onset Date:
Rec V Date: 09/18/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: soreness at the injection site last; chills; fever; swelling of the tongue; swelling of the throat; headache; weakness; very sick for 4 days; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, solution for injection), dose 1 via an unspecified route of administration on 08Feb2021 (Batch/Lot number was not reported) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included allergic to shellfish (food allergy: shellfish), peanuts and different things and immune deficiency (low white blood cells), chemotherapy from an unknown date and unknown if ongoing. The patient's concomitant medications were not reported. It was reported that the patient was expected to receive the 2nd dose on 01Mar2021. However, following the first dose, the patient had soreness at the injection site last, chills, fever, swelling of the tongue, swelling of the throat, headache, weakness and very sick for 4 days on an unspecified date. It was reported that she was advised by her pharmacist to take Tylenol and Benadryl, every 4 hours to keep the fever down and to keep the tongue and throat from closing. Therapeutic measures were taken as a result of soreness at the injection site last, fever, swelling of the tongue, swelling of the throat, headache, weakness and very sick for 4 days. Outcome of all events were unknown. Information about lot/ batch number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1712346
Sex: F
Age:
State: FL

Vax Date: 02/18/2021
Onset Date:
Rec V Date: 09/18/2021
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: tenderness at the site of injection; developed a rash on the same arm where the injection was; sore; Allergic reaction; had little bumps on it; it is kind of irritated; This is a spontaneous report from a contactable consumer (patient herself). A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot number was not reported), via an unspecified route of administration on 18Feb2021 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 an allergic reaction to the Pfizer COVID-19 vaccine. She reported that she had the Pfizer COVID-19 vaccine injection and was a little sore, and allergic reaction area had little bumps on it; since then there are more bumps on it and it is kind of irritated. She called to ask what to do or to put on the allergic reaction. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1712347
Sex: F
Age:
State: NM

Vax Date: 02/19/2021
Onset Date: 02/19/2021
Rec V Date: 09/18/2021
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: Test Date: 20210129; Test Name: BP; Result Unstructured Data: Test Result:136/66; Test Date: 20210219; Test Name: BP; Result Unstructured Data: Test Result:142/80; Test Date: 20210129; Test Name: HR; Result Unstructured Data: Test Result:89; Test Date: 20210129; Test Name: SaO2; Test Result: 95 %; Test Date: 20210219; Test Name: SaO2; Test Result: 100 %

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: Approximately 5 minutes after vaccine administered pt became flushed; Nauseated; Lightheadedness; This is a spontaneous report from a contactable pharmacist. A 42-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EN6198), dose 2 intramuscular on 19Feb2021 13:45 (at the age of 42-year-old) as dose 2, single for COVID-19 immunization. Medical history included ongoing migraine. Concomitant medication(s) included fish oil (capsule); acetylsalicylic acid, butalbital, caffeine, phenacetin (FIORINAL [ACETYLSALICYLIC ACID; BUTALBITAL; CAFFEINE; PHENACETIN]) and multivitamin taken for an unspecified indication, start and stop date were not reported (other medications the patient received within 2 weeks of vaccination). Pregnancy was unknown at that time of vaccination. The patient previously received first dose of BNT162B2 (Lot number: EL3246), intramuscular administered on 29Jan2021 for COVID-19 immunization and experienced lightheaded, felt dizzy, nausea, ceftriaxone for allergy, nausea, diaphoresis, Imitrex for allergy and nitrofurantoin for allergy, rash, nausea, vomiting, headache. Prior to vaccination, the patient diagnosed with COVID-19 was unknown. Since the vaccination, the patient had been tested for COVID-19 was unknown. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Facility where the most recent COVID-19 vaccine was administered at Public Health Clinic. On 19Feb2021 13:50, approximately 5 minutes after vaccine administered patient became flushed, nauseated and lightheadedness. Patient alerted observer and medical assistant called for transfer of the patient to the first aid office. Patient then evaluated by EMS on duty. At 14:35, Patient symptoms resolved, and patient was cleared by EMS to discharge home. Ambulated on own without weakness. There was no treatment for the events. The patient underwent lab tests and procedures which included BP: 136/66 on 29Jan2021, 142/80 on 19Feb2021, HR: 89 on 29Jan2021, SaO2: 95 % on 29Jan2021, 100 % on 19Feb2021. The clinical outcome of events was recovered on 19Feb2021 14:35. Follow up attempts are completed. No further information is expected.

Other Meds: FISH OIL; FIORINAL [ACETYLSALICYLIC ACID;BUTALBITAL;CAFFEINE;PHENACETIN]

Current Illness: Migraine

ID: 1712348
Sex: F
Age:
State: OH

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 09/18/2021
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: Roof of her mouth feels like when you've eaten something that is too hot/roof of her mouth feels burned; her tongue was itching and burning; her tongue was itching and burning; Her ears did same thing, itching and burning; She had itching and burning down the side of her neck like when you get sinus drainage itching and burning; She had itching and burning down the side of her neck like when you get sinus drainage itching and burning; itching on the roof of her mouth; slight tongue swelling; bad taste in her mouth /She could taste the vaccine, it was really nasty; This is a spontaneous case received from a contactable consumer (patient). A 69-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, lot number: EN6202, expiration date: 30Jun2021) via an unspecified route of administration in arm left on 25Feb2021 14:37 (age at vaccination 69-year-old) as DOSE 1, SINGLE for COVID-19 immunisation. The patient's medical history included ongoing diabetic (She does not require medication at this point for this condition. Onset date several years ago, probably 4-5 years ago. She was able to control it) and allergy to statins (she cannot take more than 20 mg/day or she hurts so. Additional statin product names/Lots/NDCs/Expiries: Unknown, she does not have products with her at time of call which are dispensed in white manufacturer bottles by pharmacy company- includes Atorvastatin). The patient had previously taken water pill. Concomitant medications include propranolol hydrochloride (INDERAL), ATORVASTATIN, HYDROCHLOROTHIAZIDE, acetylsalicylic acid (BABY ASPIRIN), VITAMIN D NOS. Historical vaccine include flu shot. History of all previous immunization with the Pfizer vaccine considered as suspect (or patient age at first and subsequent immunizations if dates of birth or immunizations are not available) was reported as none. Additional Vaccines Administered on Same Date of the Pfizer Suspect: Vaccines If applicable, list all vaccines administered on same date with the Pfizer vaccine considered as suspect was 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 AE(s) was reported as none. Relevant tests were reported as none. On 25Feb2021 15:07, the patient experienced a bad taste in her mouth and at 15:37 itching on the roof of her mouth, her tongue was itching and burning and had slight tongue swelling. Her tongue started itching and burning; and it was like her ears did same thing, itching and burning. She had itching and burning down the side of her neck like when you get sinus drainage itching and burning. On 26Feb2021, the patient stated roof of her mouth feels like when you have eaten something that is too hot. The patient called her family physician's office regarding these events and talked to the nurse. The nurse said to call Pfizer because she did not know what to do. The nurse said she had not heard of that reaction before. Consumer reported she researched last night and has not seen that either. Emergency room and Physician office visit was reported as none. The outcome of the event (bad taste in her mouth) was unknown, event (itching on the roof of her mouth, her tongue was itching and burning, slight tongue swelling) was recovered on 25Feb2021 19:30 and event, event (roof of her mouth feels like when you've eaten something that is too hot) was recovered with sequel. No follow-up attempts are possible. No further information was expected.

Other Meds: INDERAL; ATORVASTATIN; HYDROCHLOROTHIAZIDE; BABY ASPIRIN; VITAMIN D NOS

Current Illness: Diabetic (several years ago, probably 4-5 years ago. She is able to control it.)

ID: 1712349
Sex: F
Age:
State: IL

Vax Date: 02/23/2021
Onset Date: 02/26/2021
Rec V Date: 09/18/2021
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: red patch on her arm; This is a spontaneous report from a contactable consumer (patient). A 82-years-old female patient received first dose of bnt162b2(PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, lot number: unknown) via an unspecified route of administration on 23Feb2021 as dose 2, single for COVID-19 immunisation. The patient medical history included she did have reactions to a lot of medications, not like flu shots, but she does reaction to some medications, allergy medicines in particular. Stated did not react to pneumonia vaccine and verbalizes it did not itch. Concomitant medication was not reported. The patient received first dose of bnt162b2(PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, lot number: unknown) via an unspecified route of administration as dose 1, single for COVID-19 immunisation. Caller stated that she got her second Pfizer shot on Tuesday (23Feb2021). Caller stated that she was a person that had to wait 30 minutes after getting a new medicine, and so far everything was so good. But today (26feb2021), caller discovered a red patch on her arm, the arm she received the injection in, but not right at the injection site, it was a couple inches or so below that. Caller stated that it was about a half dollar, a silver dollar size, and it was not bright red but it was noticeable. Caller was wondering if this was a known side effect of the product. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1712350
Sex: M
Age:
State:

Vax Date: 02/11/2021
Onset Date: 02/25/2021
Rec V Date: 09/18/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: Constant runny nose; feeling sluggish; joint stiffness; lungs and chest were tight/sore; weakness; sweat; This is a spontaneous report from a contactable consumer. This male consumer (patient) reported. A male patient with unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, batch/lot number: unknown) via unknown route of administration on 11Feb2021 as DOSE 2, SINGLE for COVID-19 immunisation. The patient's medical history included triple bypass, carotid artery surgery, a thyroid condition, and diabetes. The patient stated that he was rather active and "not a couch potato". The patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, batch/lot number: unknown) via unknown route of administration on 21Jan2021 as DOSE 1, SINGLE for COVID-19 immunisation. After first dose patient had a sore arm and a change to his bowel movements which were daily and softer resulting in diarrhea for the remainder of the month, he had "never been that regular in his life", end of January his BMs changed. The patient also reported having had a "constant runny nose" since the first dose that was ongoing. After receiving the second shot on 11Feb2021 on day 21 as directed and had been "feeling sluggish" since. Last night, 25Feb2021, the patient was sweat so much he "completely soaked the bed", he had joint stiffness and weakness, and his lungs and chest were tight/sore when he took a deep breath. His symptoms have "kind of cleared up" but he was "just don't feel right" today. At the time of this report the outcome of the event constant runny nose was not recovered and other events were unknown. Information on the lot/batch number had been requested. Follow-up attempts were completed. No further information was expected.

Other Meds:

Current Illness:

ID: 1712351
Sex: F
Age:
State: CA

Vax Date: 02/26/2021
Onset Date:
Rec V Date: 09/18/2021
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: She mentioned that she needle phobia and was already anxious when she got to their facility.; She mentioned that she had difficulty in breathing because of her double mask.; she felt light headed.; her lips started to tingle; This is a spontaneous report from a contactable consumer (patient). A female patient (Age: 54; Unit: Unknown) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/Lot Number: unknown, Expiry date: unknown), via an unspecified route of administration on 26Feb2021 as dose 1, single for covid-19 immunisation. The patient medical history included needle phobia and concomitant medications were not reported. The patient reported, she received the 1st dose of the Pfizer vaccine about an hour ago today. She mentioned that she had needle phobia and was already anxious when she got to their facility. She mentioned that the person who injected her was really quick that she didn't feel it. They made her stay for 20 minutes and she was fine, she mentioned that she had difficulty in breathing because of her double mask. As she was walking to her car, she felt lightheaded. As she got in the car, her lips started to tingle. The outcome of events was unknown. Information about Lot/Batch request has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1712352
Sex: M
Age:
State: AZ

Vax Date: 02/12/2021
Onset Date: 02/12/2021
Rec V Date: 09/18/2021
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: Dizziness; weakness; Inflammation in body; headaches; pain in joint and muscles; sleeplessness; My eyes would blur if I read, watched TV or looking at I Phone or computer; brain (felt like my body and brain were on fire); This is a spontaneous report from a contactable consumer. A 70-year-old male patient received BNT162B2 (BNT162B2, Pfizer-BIONTECH, COVIF-19 Vaccine, Solution for injection, Lot number: EL9267 and expiration date: Not reported), via an unspecified route of administration, administered in Arm Left on 12Feb2021 09:45 as SINGLE DOSE for COVID-19 IMMUNISATION. The patient medical history included Polymyalgia, Rheumatica, Herpes, Afib, BPH, Sulfa allergy. Covid prior vaccination was No. Concomitant medication included prednisone, hydroxychloroquine silodosin. The patient previously took levofloxacin (LEVAQUIN), statin, metoprolol, fluoxetine, Nortriptyline, pregabalin (LYRICA), propafenone, Zolpidem and had allergies to these drugs. It was reported that the patient had experienced Dizziness, weakness, inflammation in body, brain (felt like my body and brain were on fire),headaches, pain in joints and muscles, sleeplessness. My eyes would blur if I read, watched TV or looking at I Phone or computer all on 12Feb2021 13.00. Covid tested post vaccination was No. Therapeutic measures were taken as a result of events. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: PREDNISONE; HYDROXYCHLOROQUINE; SILODOSIN

Current Illness:

ID: 1712353
Sex: F
Age:
State: CA

Vax Date: 02/25/2021
Onset Date:
Rec V Date: 09/18/2021
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: It (arm) does not hurt so bad; there is some discomfort/arm was sore; hand started to itch for about 3 minutes after; headache; This is a spontaneous report from a contactable consumer (patient). A 70-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot Number: EN6201, Expiry Date: Unknown), dose 1 via an unspecified route of administration on 25Feb2021 (at the age of 70-years-old) as DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced it (arm) does not hurt so bad; there is some discomfort/arm was sore, hand started to itch for about 3 minutes after and headache. Reporter received the Pfizer-BioNTech COVID-19 Vaccine first dose yesterday (on 25Feb2021). Reporter had been advised by the vaccination Center to only take Tylenol but was seeking clarification. Reporter was also asking for the "time period to wait before" she can take her daily low dose aspirin? Reporter mentioned that her "arm hurts when I lift", and that her "hand started to itch for about 3 minutes after". Reporter said that she had "nothing to report". Her arm was sore, and she took Tylenol. She wanted to confirm when she should take a low dose of Aspirin or ibuprofen as she was regularly having a headache. She said, doctor had me on daily low dose Aspirin regimen, so I did not take that low dose Aspirin today because she said no Aspirin. Reporter stated, "Well I had my first dose of the vaccine by Pfizer (clarified Covid 19 vaccine), yesterday and I was told if I had any pain in my arm that was so uncomfortable that I needed to take something, that I should take Tylenol and not take aspirin and not take Ibuprofen or Aleve or anything, to take Tylenol only. This is my question, my arm does not hurt, at least it does not hurt so bad that I would take anything for it at all. I can tell you the truth, there was some discomfort but nothing to complaint about, but I am a senior citizen, and my doctor has me on daily low dose Aspirin regimen so, I did not take that low dose Aspirin today because she said no Aspirin. So, my question is how many days do I have to wait before I can take aspirin or Ibuprofen for a headache and go back to taking my Aspirin or just take Ibuprofen for back ache or for muscle pull or whatever, how many days?" Reporter stated, "I just want to know when I can take aspirin again that is all. That is all no pain, nothing. do not take this shot if you are allergic to vaccine or its ingredients but you do not tell us the ingredients until you give that person the shot." Therapeutic measures were taken as a result of the events. Outcome of all the events were unknown. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1712354
Sex: F
Age:
State: CA

Vax Date: 02/24/2021
Onset Date: 02/25/2021
Rec V Date: 09/18/2021
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: 20210225; Test Name: Fever; Result Unstructured Data: Test Result:101.5

Allergies:

Symptom List: Tremor

Symptoms: Chills; Fever 101.5; Headache; Nausea; joint ache; Injection Site: red; Injection Site swollen; Injection Site pain; This is a spontaneous report from a contactable consumer (patient). A 67-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EM9809), via an unspecified route of administration, administered in Arm Left on 24Feb2021 17:15 (at the age of 67-year-old) as dose 2, single for covid-19 immunisation. Medical history included High Blood Pressure, High cholesterol, obesity. Known allergies were reported as no. The concomitant medications were not reported. Patient did not receive any other vaccine in four weeks. Other medications in two weeks were reported as High Blood Pressure, High Cholesterol meds. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EN5318), via an unspecified route of administration, administered in Arm Left on 03Feb2021 17:15 (at the age of 67-year-old) as dose 1, single for covid-19 immunisation. Patient did not have covid prior vaccination and covid was not tested post vaccination. The patient experienced chills, fever 101.5, headache, nausea, joint ache, injection site: red, injection site swollen, injection site pain on 25Feb2021 10:00. The patient underwent lab tests and procedures which included body temperature: 101.5 on 25Feb2021. Patient did not receive any treatment for adverse events. The outcome of all events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1712355
Sex: F
Age:
State: CO

Vax Date: 02/19/2021
Onset Date: 02/19/2021
Rec V Date: 09/18/2021
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: her throat began to feel thick and she felt shaky; Within about 5 minutes after the injection my face started tingling; felt like I had a bad sunburn; The morning after I had the typical vaccine side effects of sore arm; A little body aches; This is a spontaneous report from a contactable consumer (patient herself). A 53-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection and lot number: EN6201) via an unspecified route of administration in Left arm on 19Feb2021 16:30 as single dose for COVID-19 immunisation. Patient medical history included breast cancer in 2014 and chemo. Concomitant medications included colecalciferol (VITAMIN D 3) and exemestane. Patient previously took Docetaxel and experienced with Severe anaphylaxis from chemotherapy. On 19Feb2021 16:45 patient stated that about 15 minutes after the injection her face started tingling and soon after felt like she had a bad sunburn. At the same time her throat began to feel thick and she felt shaky. She wasn't shaking but she felt shaky on the inside. She could talk and breathe ok but her throat felt thick inside. After she went home, the thick throat feeling went away in about 40 minutes and the sunburn feeling was gone by the next morning. The morning after she had the typical vaccine side effects of sore arm and a little body aches. Throat and face felt fine. Treatment was not received for events. Outcome of events was recovered on an unspecified date in 2021.

Other Meds: VITAMIN D 3; EXEMESTANE

Current Illness:

ID: 1712356
Sex: M
Age:
State:

Vax Date: 02/24/2021
Onset Date: 02/01/2021
Rec V Date: 09/18/2021
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: pharmacist accidentally injected a COVID vaccine to a 4 year old on 2/24.; pharmacist accidentally injected a COVID vaccine to a 4 year old on 2/24.; fever; This is a spontaneous report from a contactable pharmacist via medical information team. A 4-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number was not reported, Expiry date was not reported), via an unspecified route of administration on 24Feb2021 as DOSE NUMBER UNKNOWN, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date in Feb2021, the child experienced fever within 24 hours. The reporter stated, that at one of the mass immunization site, the pharmacist accidentally injected a COVID vaccine to a 4-year-old on 24Feb. The child experienced fever within 24 hours. The child was now acting normal. They are wondering how they should proceed and what advice to be given. The outcome of the event fever was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1712357
Sex: M
Age:
State: MD

Vax Date: 02/20/2021
Onset Date: 02/20/2021
Rec V Date: 09/18/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Oral lesions; This is a spontaneous report from a contactable other healthcare professional (patient). A 69-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection lot Number: EN6198), intramuscular, administered in right arm on 20Feb2021 at 10:15 (age at the time of vaccination was 69 years) as single dose for COVID-19 immunisation. Other medical history included coronary artery disease from an unknown date and unknown if ongoing and Known allergies were reported as no. The patient's concomitant medications were not reported. If other vaccine in four weeks was reported as no and the patient did not have COVID prior vaccination. On 20Feb2021 at 19:15, the patient experienced oral lesions. AE treatment was reported as no and the patient was not tested for COVID post vaccination. The outcome of the event was not recovered. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1712358
Sex: F
Age:
State: VA

Vax Date: 02/03/2021
Onset Date: 02/04/2021
Rec V Date: 09/18/2021
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: temp; Result Unstructured Data: Test Result:fluctuating; Test Date: 20210223; Test Name: Blood test; Test Result: Negative ; Comments: covid19 IgM/IgG; Test Date: 20210223; Test Name: Nasal Swab; Test Result: Negative

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: fluctuating temp; Musculoskeletal pain to Left side of body: Mainly left upper body; The injected site was sore, mild; Malaise; Extreme fatigue; brain fog; intermittent confusion; severe pain to Lt shoulder and clavicle; severe pain to Lt shoulder and clavicle; This is a spontaneous report from a contactable nurse (patient herself). A 50-years-old non pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9264), via intramuscular route, administered in left arm on 03Feb2021 11:45 (age at vaccination: 50 years) as DOSE 2, SINGLE for covid-19 immunisation. The patient's medical history included rheumatic fever, erythema nodosum, osteonecrosis, cataract and depression. Concomitant medication(s) included bupropion; apap; colecalciferol (VITAMIN D); ibuprofen (MOTRIN). The patient's historical vaccine included bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EL3249) via intramuscular route, administered in left arm on 13Jan2021 11:00 as DOSE 1, SINGLE for covid-19 immunisation and experienced musculoskeletal pain. The patient did not receive any other vaccine in four weeks. The patient was allergic to ciprofloxacin and Bactrim. On 04Feb2021 02:00, 12 hours after the vaccination, the patient experienced fluctuating temp, musculoskeletal pain to left side of body: mainly left upper body, the injected site was sore, mild, malaise, extreme fatigue, brain fog, intermittent confusion, 17 hours later woke up with severe pain to shoulder and clavicle. The musculoskeletal pain was continuing and the pain was at various sites, forms and levels. Severe-moderate/shooting and needle pain, moderate/radiating pain, moderate-mild/dull pain, mild/annoying persistent uncomfortable pain. The adverse event resulted in physician's office visit. The patient did not receive any treatment for the adverse event. The patient was not diagnosed with covid-19 prior to vaccination nor was tested since vaccination. On 23Feb2021, the patient underwent lab tests and procedures which included sars-cov-2 antibody test which was negative and body temperature was fluctuating. The outcome of the events was recovering. No follow-up attempts are needed. No further information is expected.

Other Meds: BUPROPION; APAP; VITAMIN D [COLECALCIFEROL]; MOTRIN [IBUPROFEN]

Current Illness:

ID: 1712359
Sex: M
Age:
State:

Vax Date: 02/08/2021
Onset Date:
Rec V Date: 09/18/2021
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: Something odd is going on with toes; Sort of looks like COVID toes, a mild case but not extreme; This is a spontaneous report from a contactable consumer (patient wife). A male patient of an unspecified age received BNT162B2(PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot Number: EL9263, as reported), via an unspecified route of administration on 08Feb2021 (Lot Number: EM9809) as dose number unknown single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Patient wife stated, she was actually going to put patient husband on. It is really his question. We both had the Pfizer COVID-19 vaccine about 2 weeks ago and coincidently, he felt fine and everything still does feel fine but something odd is going on with his toes. And patient know there is something called COVID toes and we looked it up online, that's sort of what it looks like, a mild case but not extreme. But really our question is related to, could this be a side effect from the vaccine. I will put him on. When requested for permission to probe questions for a safety report, patient stated not sure what questions was answering, what questions are you talking about informed that the questions would be related to demographic details, medical history, patient stated, this is taking way too long. I'll have to call back patient have the number and the option and will call back in a later date. Outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1712360
Sex: F
Age:
State: OK

Vax Date: 02/27/2021
Onset Date:
Rec V Date: 09/18/2021
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 in face; Swelling in tongue; Swelling in Throat; sweating; Dizziness; This is a spontaneous report from a contactable consumer (patient). A 35-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: En6206), via an unspecified route of administration in right arm on 27Feb2021 at 13:45 (at the age of 35 years old) as single dose for COVID-19 immunisation. Medical history included fatty liver disease. The patient known allergies included demerol and shellfish. The patient's concomitant medications were not reported. The patient did not receive any other medications in two weeks. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient hasn't been tested for COVID-19. The patient experienced swelling in face, tongue, throat, sweating, and dizziness on an unspecified date. Had to ambulance received EpiPen's, Benadryl, and other medications. Was in the hospital for 6 hours. Therapeutic measures were taken as a result of swelling in face, swelling in tongue, swelling in throat, sweating, dizziness with EpiPen's, Benadryl, tylenol, steroids and other med. The event resulted in: Doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care. The outcome of events was recovering. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1712361
Sex: M
Age:
State: CT

Vax Date: 02/28/2021
Onset Date: 01/29/2021
Rec V Date: 09/18/2021
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: There was accompanied pain in the knee and ankles; There was accompanied pain in the knee and ankles; I had varicose veins in my right leg that after the vaccination became very badly swollen and then one appeared in my left leg.; This is a spontaneous report from a contactable consumer or other non hcp. A 76-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number: Batch/Lot Number: EL9261; Expiration Date: unknown), dose 1 via an intramuscular in Arm Left on 27JAN2021 11:45 as single dose and bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number: Batch/Lot Number: EN6200; Expiration Date: unknown), dose 2 via intramuscular in Arm Left on 28Feb2021 11:40 as single dose for COVID-19 immunization. Medical history included blood pressure increased from an unknown date and Kidney Stone from 28Nov2017 to 4Feb2018. Patient surgical procedure includes Catheter operation 1Dec2017, Removal 1 , 15Jan2018 and Removal 2, 14Feb2018 The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient's concomitant medications were not reported. On an unspecified date, the patient experienced varicose veins in right leg that after the vaccination became very badly swollen and then one appeared in left leg, accompanied pain in the knee and ankles. The outcome of the events was not recovered. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1712362
Sex: F
Age:
State: MA

Vax Date: 01/26/2021
Onset Date: 01/01/2021
Rec V Date: 09/18/2021
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: runny nose; Light Arthralgia, upper back/shoulders, progressing to arms, wrists, hands; Fatigue; unable to grip and hold things w/ hands; sleeping 10 h; All sxs (Symptoms) w/ worsening progression; This is a spontaneous report from a contactable Nurse. This 53-year-old female Nurse (patient) reported that. A 53-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot Number: EK9231), dose 1 via an unspecified route of administration, administered in Arm Left on 26Jan2021 12:30 as dose 1, single for covid-19 immunisation. Medical history included ewing's sarcoma from an unknown date and unknown if ongoing as a teen. Concomitant medication included omeprazole 20 mg taken for an unspecified indication, start and stop date were not reported; amlodipine 2.5 mg taken for an unspecified indication, start and stop date were not reported. It was Unknown if patient had COVID prior vaccination. No COVID tested post vaccination. No other vaccine in four weeks. Patient was not pregnant at the time of vaccination. It was reported that patient experienced Day 1: constant runny nose. 3d after dose 1: 5pm: runny nose, Light Arthralgia, upper back/shoulders, progressing to arms, wrists, hands. Fatigue. All sxs (Symptoms) w/ worsening progression w/i 2h, unable to grip and hold things w/ hands, in bed by 7 pm and sleeping 10 h. This occurs daily at the same time (5p). Upon awakening the following am, I am back to my normal self / feeling well. It was reported that patient received treatment: Ibuprofen- No relief of sxs (Symptoms). The outcome of event all sxs (symptoms) w/ worsening progression was unknown and outcome of al other events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: OMEPRAZOLE; AMLODIPINE

Current Illness:

ID: 1712363
Sex: F
Age:
State:

Vax Date: 02/26/2021
Onset Date: 02/27/2021
Rec V Date: 09/18/2021
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: itchy eyes; I started with sneezing and drippy nose; Sore arm; I started with sneezing and drippy nose; It's just like sinus and allergy; It's just like sinus and allergy; This is a spontaneous report from a contactable consumer (patient). A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EN6198, UPC, NDC number and Expiry date: Unknown), via an unspecified route of administration on 26Feb2021 as DOSE 1, SINGLE for COVID-19 immunisation. Medical history included allergy to pollen and asthma from an unknown date and unknown if ongoing. Concomitant medications were not reported. The patient got the first dose of the Pfizer COVID-19 vaccine on Friday morning (26Feb2021). Yesterday (27Feb2021), patient started to have adverse events like itch eyes, runny nose and drippy nose, and sneezing. The patient was fine with the sore arm. The patient said this allergic reaction maybe attributed to her allergy to pollen. The patient said other than the reactions patient mentioned, she felt fine, patient had no headache, etc. The patient mentioned her reaction got worse this morning (28Feb2021). The patient wanted to know if it was ok to take Claritin or other anti-allergy medications. The patient wanted to manage her reaction because it might flare up and the patient might have trouble because patient also has asthma. The patient had allergies anyways like with pollen going on and on now. The patient just wants to make sure because patient got up this morning and it worst. The patient does not have any other symptoms, there was no fever, and there was no pain, nothing like that. It was just like sinus and allergy. The patient just wants to make sure if it was okay patient had that. The patient did not take any Tylenol for the soreness for arm, the patient has not taken anything like that. I just want to make sure that it is okay to take maybe Zyrtec or Claritin, something like that. Outcome of the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1712364
Sex: F
Age:
State: NC

Vax Date: 02/18/2021
Onset Date: 02/01/2021
Rec V Date: 09/18/2021
Hospital:

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

Lab Data: Test Date: 20210218; Test Name: Temp 100. Temp 97; Result Unstructured Data: Test Result:Temp 100. Temp 97; Test Date: 20210218; Test Name: Wt loss 99 lbs down to 95 lb; Result Unstructured Data: Test Result:Wt loss 99 lbs down to 95 lbChills

Allergies:

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

Symptoms: headache; Wt loss 99 lbs down to 95 lbChills; diarrhea; dizziness; Nausea; Chills; Weak; Indigestion; back pain; Hip pain; Temp 100. Temp 97; Night sweat; malaise; extreme fatigue; dehydration; abdominal pain; loss of appetite; excessive thirst; joint pain; : This is a spontaneous report from a contactable other hcp (patient). A 67-year-old non-pregnant female patient received second dose of bnt162b2 (BNT162B2 PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot number: EN6200), via an unspecified route of administration in arm right on 18Feb2021 at 09:30 (at the age of 67-years-old) as dose 2, single for COVID-19 immunization. The medical history included allergies to SULFA Vaccine. The concomitant medications of the patient included ascorbic acid, dexpanthenol, ergocalciferol, nicotinamide, pyridoxine hydrochloride, retinol, riboflavin, thiamine hydrochloride, tocopheryl acetate (MVI [ASCORBIC ACID;DEXPANTHENOL;ERGOCALCIFEROL;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RETINOL;RIBOFLAVIN;THIAMINE HYDROCHLORIDE;TOCOPHERYL ACETATE]), calcium (CALCIUM), ergocalciferol (VIT D) and Biest Cream all taken for an unspecified indication, start and stop date were not reported. The patient previously received first dose of BNT162B2 PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Batch/Lot number: EL8982), via an unspecified route of administration in arm right on 27Jan2021 at 09:30 as single dose for COVID-19 immunisation and her arm was real sore. The patient was not pregnant at the time of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the covid vaccine. Prior to vaccination, the patient was not diagnosed with covid-19. Since the vaccination, the patient not been tested with covid-19. On an unspecified date in Feb2021, the patient experienced dehydration, abdominal pain, loss of appetite, excessive thirst, joint pain, malaise, extreme fatigue, on 18Feb2021, the patient experienced Wt loss 99 lbs down to 95 lbChills, diarrhea, dizziness, Nausea, Chills, Weak, Indigestion, back pain, Hip pain, Temp 100. Temp 97, Night sweat and on 19Feb2021, the patient experienced headache. The patient reported that she didn't have any symptoms after receiving the first dose of the vaccine. She was only 90 pounds maybe she did not need the second dose. She believed the decision to give one or two doses should be evaluated according to the individual's weight. An individual weighing less than a certain number only needs to receive one dose and not two. She was extremely disappointed and regretted getting the shot. She thought all those side effects are related to the vaccine otherwise she was a healthy person. She felt like a mess because she must call the doctor and get tested for COVID because she doesn't know how to fix that. She was hoping everyday she will get better. She had reported abdominal pain, loss of appetite, dehydration, excessive thirst, headache and joint pain. She had diarrhea which lasted 2-3 days and dizziness which occurred 15 hours post vaccination. She also reported malaise and extreme fatigue as one of the biggest side effects after receiving the second dose. She also lost weight. She went from 102 pound to 95 pounds. She stated she was certain all these side effects are related to the vaccine. She asked are there a lot of people like her calling to report side effects after the second dose? she had been very sick since she had gotten it, it started 15 hours after the injection. Her temperature was 100.5, she had chills, dizziness, then the next day she had headache, weakness, nausea. Then Sunday she had nausea, diarrhea 2-3 times and Monday she had weakness, she was nauseous and had abdominal discomfort. previous night she had 2 profuse sweating spells, her temperature was 97 that morning. And people keep saying to her do you have COVID? The first dose she did great other than her arm was real sore. She was very healthy, she goes to the gym, she works out, she does not know what to do if she should go down and tested at the hospital. She had never been tested and she doesn't think she had COVID, she asked the shot cant give COVID can it. The patient underwent lab tests and procedures that included Wt loss 99 lbs down to 95lb: Wt loss 99 lbs down to 95 lb on 18Feb2021 and Temp 100. Temp 97 on 18Feb2021. The patient received no treatment for the events. The outcome of the events Wt loss 99 lbs down to 95 lb Chills, diarrhea, dizziness, Nausea, Chills, Weak, Indigestion, back pain, Hip pain, Temp 100. Temp 97, Night sweat was reported as not resolved and the outcome of the events dehydration, abdominal pain, loss of appetite, excessive thirst, headache, joint pain, malaise, extreme fatigue was reported as unknown. No follow-up attempts are needed. No further information is expected.

Other Meds: MVI [ASCORBIC ACID;DEXPANTHENOL;ERGOCALCIFEROL;NICOTINAMIDE;PYRIDOXINE HYDROCHLORIDE;RETINOL;RIBOFLA; CALCIUM; VIT D

Current Illness:

ID: 1712365
Sex: F
Age:
State: MD

Vax Date: 02/20/2021
Onset Date: 02/21/2021
Rec V Date: 09/18/2021
Hospital:

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

Lab Data: Test Date: 20210226; Test Name: Nasal Swap; Test Result: Negative

Allergies:

Symptom List: Vomiting

Symptoms: disoriented; flu-like symptoms; Tired; weak; achey; Low-grade fever; This is a spontaneous report from a contactable consumer (patient). A 77-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: not reported), dose 2 via an unspecified route of administration, administered in Arm Left on 20Feb2021 at 10:15 (at the age of 77-years-old) as dose 2, single for covid-19 immunisation. Medical history included chronic obstructive pulmonary disease (COPD) and psoriasis. Patient had no known allergies. The patient received no other vaccine in four weeks. Concomitant medication included fluticasone furoate, umeclidinium bromide, vilanterol trifenatate (TRELEGY ELLIPTA). Historical vaccine included bnt162b2 (Batch/Lot Number: not reported) on 30Jan2021 at 12:00 pm as dose 1 in Left arm for covid-19 immunisation. On 21Feb2021, the patient experienced disoriented, flu-like symptoms, tired, weak, achey and low-grade fever. The patient underwent lab tests and procedures which included sars-cov-2 antibody test: negative on 26Feb2021. Facility type vaccine was a school or Health Clinic. Treatment was given for the events. The patient was not covid prior vaccination. The patient tested for covid post vaccination. Outcome of the events were not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: TRELEGY ELLIPTA

Current Illness:

ID: 1712366
Sex: F
Age:
State: WI

Vax Date: 02/17/2021
Onset Date: 02/17/2021
Rec V Date: 09/18/2021
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: dizziness; her arm became floppy; This is a spontaneous report from a contactable consumer or other non hcp (patient) via Pfizer-sponsored program. A female patient of an unspecified age received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, formulation: solution for injection) via an unspecified route of administration on 17Feb2021 (last Wednesday) as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. That evening, she experienced dizziness. The dizziness continued until it is hard for her to do anything. She also mentioned her arm became floppy. On 17Feb2021 at evening, the patient experienced dizziness which continued until it is hard for her to do anything and also her arm became floppy. The outcome of the events was unknown. Information about Lot/Batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1712367
Sex: M
Age:
State: AL

Vax Date: 02/27/2021
Onset Date: 02/27/2021
Rec V Date: 09/18/2021
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: Very sore left arm - difficult movement; Very sore left arm - difficult movement; Sore joints; Achy muscles; fever; chills; anxiety; insomnia; malaise; mild nausea; dizziness; headache; This is a spontaneous report from a contactable consumer (patient). A 44-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number: EN6200, Expiration Date: not reported), via an unspecified route of administration in left arm on 27Feb2021 07:30 as dose 2, single for COVID-19 immunization (at the age of 44-year-old). Medical history included hypertension, anxiety, other managed conditions and allergies to erythromycin. Patient did not receive other vaccine in four weeks. Patient had numerous prescriptions in two weeks. The patient previously took BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number: EM9809, Expiration Date: not reported), via an unspecified route of administration in left arm on 06Feb2021 11:30 as dose 1, single for COVID-19 immunization. Patient had no covid prior vaccination and was not covid tested post vaccination. The patient experienced very sore left arm - difficult movement, sore joints, achy muscles, fever, chills, anxiety, insomnia, malaise, mild nausea, dizziness, headache on 27Feb2021 14:00. All symptoms began to resolve and decrease after 24 hours, though, some muscle aches and headache mildly remain. The patient did not receive treatment for the events. The outcome of the events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1712368
Sex: F
Age:
State: CA

Vax Date:
Onset Date:
Rec V Date: 09/18/2021
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: she hurt her back after getting the first dose of the covid vaccine; This is a spontaneous report from a contactable consumer or other non-HCP (patient herself) via Pfizer-sponsored program. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number-UNKNOWN) via an unspecified route of administration on an unspecified date as dose 1, single for COVID-19 immunization. Patient medical history and concomitant medications were not reported. The reporter stated that patient hurt her back after getting the first dose of the covid vaccine on an unspecified date and patient has not had any side effects even after her second dose. The outcome of the event was unknown. Information on lot number/batch number has been requested. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1712369
Sex: F
Age:
State: PA

Vax Date: 02/24/2021
Onset Date: 02/24/2021
Rec V Date: 09/18/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Developed chills; muscle/joint pain; nausea; tiredness; fever; headache; dizziness; general weakness; This is the spontaneous report from a contactable consumer (patient) reported for herself. A 67-years-old non-pregnant female patient received BNT162B2 (Pfizer-Biontech COVID-19 Vaccine, Solution for injection, batch/lot number: EN6201), via an unknown route of administration in left arm on 24Feb2021 at 07:15 (at the age of 67-years-old) as dose 2, single for COVID-19 immunisation at hospital. The patient's medical history included kidney stones in Dec 2021 and back issues resolved since oblation to spine done approx. 1.5 years ago. She was allergic to codeine. Concomitant medications included gabapentin (GABAPENTIN), acetylsalicylic acid (BABY ASPIRIN) and vitamin D NOS (VITAMIN D NOS); all were taken for an unknown indication from an unknown date. No other vaccine in four weeks. The patient received BNT162B2 (Pfizer-Biontech COVID-19 Vaccine, Solution for injection, batch/lot number: EL9265), via an unknown route of administration in right arm on 03Feb2021 at 07:30 (at the age of 67-years-old) as historical vaccine as dose 1, single for COVID-19 immunisation. On 24Feb2021 at 20:00, the patient developed chills, muscle/joint pain, nausea, tiredness, fever, headache, dizziness and general weakness. No covid prior vaccination. No covid tested post vaccination. No treatment received. The outcome of the events was recovering. No follow up attempts are possible. No further information is expected.

Other Meds: GABAPENTIN; BABY ASPIRIN; VITAMIN D NOS

Current Illness:

ID: 1712370
Sex: F
Age:
State: TX

Vax Date: 02/23/2021
Onset Date: 02/23/2021
Rec V Date: 09/18/2021
Hospital:

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

Lab Data: Test Date: 20210223; Test Name: temperature; Result Unstructured Data: Test Result:elevated temp 99.8; Test Date: 20210224; Test Name: temperature; Result Unstructured Data: Test Result:elevated temperature 99.8; Test Date: 20210225; Test Name: temperature; Result Unstructured Data: Test Result:elevated

Allergies:

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

Symptoms: Sore arm at injection site; Elevated temp 99.8; Generalised aches and pains; Headache; Fatigue; Malaise; Chills; This is a spontaneous report from a contactable consumer (patient). A 65-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection Batch/Lot Number: EN6201), via an unspecified route of administration, administered in Arm Left on 23Feb2021 (at the age of 65-year-old) as dose 2, single for covid-19 immunisation. Medical history included fibromyalgia, arthritis, chronic fatigue syndrome (CFIDS), asthma, guava allergy. Concomitant medication(s) included fluoxetine hydrochloride (PROZAC) taken for an unspecified indication, start and stop date were not reported; bupropion hydrochloride (WELLBUTRIN) taken for an unspecified indication, start and stop date were not reported; hydrochlorothiazide, telmisartan (TELMISARTAN HCTZ) taken for an unspecified indication, start and stop date were not reported; cetirizine hydrochloride (ZYRTEC) taken for an unspecified indication, start and stop date were not reported. Other medications in two weeks were reported as Prozac, Wellbutrin, Zyrtec, Telmisartan HCTZ. The patient previously received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: EL9265), via an unspecified route of administration, administered in Arm Left on 02Feb2021 13:15 (at the age of 65-year-old) as dose 1, single for covid-19 immunisation. Patient did not have covid prior vaccination and covid was not tested post vaccination. On 23Feb2021 18:15, the patient experienced, first 24-hour sore arm at injection site, elevated temp 99.8 with ibuprofen on board every 6 hours, Generalized aches and pains, headache, fatigue. Second day elevated temperature 99.8 was the highest, again with NSAID on board every 5-6 hours, malaise, chills, headache. Day 3 elevated temp with chills and malaise in the afternoon and evening. Day 4 feeling better. The patient underwent lab tests and procedures which included body temperature: elevated temp 99.8 on 23Feb2021, body temperature: elevated temp 99.8 on 24Feb2021, body temperature: elevated temp on 25Feb2021. The patient received Ibuprofen for elevated temperature as treatment. The outcome of all events was recovered on an unspecified date. No follow-up attempts are possible. No further information is expected.

Other Meds: PROZAC; WELLBUTRIN; TELMISARTAN HCTZ; ZYRTEC [CETIRIZINE HYDROCHLORIDE]

Current Illness:

Total 2021 VAERS Injuries: 654,986

Page last modified: 13 November 2021 9:17am