VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 10/01/2021
** VAERS DATABASE Last updated: October 1, 2021**
PLEASE CHECK BACK SOON
Download the files above while you wait.






Manufacturers

Total Manufacturer
187,133MODERNA
33,878JANSSEN
2,321PFIZER\BIONTECH
1,091GLAXOSMITHKLINE BIOLOGICALS
983UNKNOWN MANUFACTURER
363MERCK & CO. INC.
229SEQIRUS, INC.
45DYNAVAX TECHNOLOGIES CORPORATION
41NOVARTIS VACCINES AND DIAGNOSTICS
29SANOFI PASTEUR
18EMERGENT BIOSOLUTIONS
8PAXVAX
7TEVA PHARMACEUTICALS
4PFIZER\WYETH
3BERNA BIOTECH, LTD.
2SMITHKLINE BEECHAM
2INTERCELL AG
2PROTEIN SCIENCES CORPORATION
1CSL LIMITED

Incidents per State

State Total
77,548
AK1,869
AL5,581
AR3,688
AS47
AZ14,288
CA61,984
CO11,665
CT8,149
DC1,663
DE1,807
FL37,749
FM5
GA15,058
GU120
HI2,453
IA4,625
ID2,692
IL20,334
IN24,007
KS4,615
KY7,696
LA4,887
MA14,654
MD12,514
ME3,129
MH11
MI18,739
MN12,528
MO9,710
MP29
MS2,790
MT2,375
NC16,368
ND1,356
NE2,880
NH3,100
NJ17,634
NM3,916
NV4,239
NY34,355
OH19,081
OK6,195
OR8,636
PA23,083
PR2,370
QM2
RI2,088
SC6,411
SD1,212
TN9,131
TX35,174
UT4,273
VA14,937
VI64
VT1,676
WA14,909
WI11,259
WV2,388
WY861
XB5
XL1
XV2

ID: 1305305
Sex: M
Age:
State: WV

Vax Date: 03/10/2021
Onset Date:
Rec V Date: 05/11/2021
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: After my 1st dose, my mouth and lips developed cold blisters outside and inside my mouth. I had "bumps on the inside of my mouth "and "it took 7-10 days for the cold blisters to go away.; bumps "inside my mouth are still there and the size of kidney beans; After my 1st dose, my mouth and lips developed cold blisters outside and inside my mouth. I had "bumps on the inside of my mouth "and "it took 7-10 days for the cold blisters to go away.; This is a spontaneous report from a contactable consumer (the patient). This is one of the 2 report of same patient. A male patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number, Expiration date: Unknown), via an unspecified route of administration on 10Mar2021 as single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date in 2021, the patient reported "After my 1st dose, my mouth and lips developed cold blisters outside and inside my mouth (oral mucosal blistering and lip blister). I had "bumps on the inside of my mouth" (Aphthous ulcer) and "it took 7-10 days for the cold blisters to go away". He used Abbreva which was expensive." The caller stated the bumps "inside my mouth are still there and the size of kidney beans. The patient received treatment. Outcome of the events oral mucosal blistering and lip blister was recovered on unknown date in 2021 and the event aphthous ulcer was not recovered. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305306
Sex: F
Age:
State: NY

Vax Date: 04/17/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
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: This is a spontaneous report from a contactable consumer (patient). A 61-year-old female patient received BNT162B2 (COVID-19 mRNA VACCINE, solution for injection, Lot number: ER0113) via an unspecified route at arm right on 17Apr2021 in the afternoon (around 15:30) (reported as this past Saturday) as a single dose for covid-19 immunisation and diphenhydramine (Lot Number: P122793 and Expiry Date: NOV2023) for two black spots under the site and that part was swollen too, it itches. Medical history and concomitant medications were not reported. The patient received first dose of BNT162B2 (COVID-19 mRNA VACCINE, solution for injection, Lot number: ER8730) via an unspecified route at arm right on 27Mar2021 in the afternoon (around 14:00) as a single dose for covid-19 immunisation with no adverse effects. On Apr2021, patient had experienced the site under where she got it was swollen and hard and it hurt. she put ice on it for the swelling. Patient reported that it started as just one spot which turned black and then she had little black spots everywhere under the spot where the vaccine went in. She had two spots and then those spots turned black and then she has tiny spots like polka dots over her arms and when she woke up next day, she had two black spots under the site and that part was swollen too. She took 2 allergy Diphenhydramine HCl 25 mg antihistamine that morning. They are oozing and she has the little black spots on her left and her right arm, but she had the vaccine in her right arm (further stated that the black spots that are oozing and it was kind of hard under it and under the site. The spots were blacker and more discolored). Patient stated that it itches and that's why she took allergy Diphenhydramine HCl 25 mg antihistamine but that made her drowsy. Patient felt like throat was kind of dry and was feeling hot and had COVID-19 test resulted in everything okay, she didn't have COVID. Patient right deltoid and right below it, maybe 3 fingerbreadths below on the left and right side bilaterally she had blotches that appeared, and they looked red. Next day they looked more like a burn kind, when a darker person gets burned by an iron then the spot gets darker in nature. One of the spots has like a vesicle that was fluid filled kind of like a blister and it was weeping. Overnight this went from blotched to burn-like marks with one vesicles that was oozing and then there are spots dispersed through her body. On her right arm, left arm, and on her right leg as well it was like black spots. Patient does not require to visit emergency room or physician office for the events. Outcome for the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305307
Sex: U
Age:
State: MD

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
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: a sore arm; This is a spontaneous report from a contactable consumer (patient) via Pfizer sponsored program . A 64-year-old patient of unspecified gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration from an unknown date (Lot#: not provided) at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient got a sore arm after received the Pfizer vaccine on an unspecified date, there is no any other issue with it. Event outcome was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1305308
Sex: U
Age:
State: SD

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
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: I was just kind of mopey; This is a spontaneous report from a Pfizer Sponsored Program via a contactable consumer (patient). A 76-years-old patient of an unspecified gender received second dose of bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine), 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. Patient just wanna thank you for the vaccine, got em both and feeling very safe. Just on the second shot patient was just kind of mopey but other than that was wonderful. Event outcome was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305309
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Developed a sore arm; chills; overall not feeling well.; This is a spontaneous report received from a contactable consumer (patient) via Medical Information Team. A female patient of an unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunisation. Medical history included hypertension. Concomitant medication included amlodipine taken for hypertension. On an unspecified date, the patient experienced a sore arm, chills, soreness and just overall not feeling well. Patient wants to know if she can take tylenol for the side effects. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained

Other Meds: AMLODIPINE

Current Illness:

ID: 1305310
Sex: M
Age:
State: NJ

Vax Date: 04/20/2021
Onset Date: 04/21/2021
Rec V Date: 05/11/2021
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: Sore arm; it was just some discomfort; Feeling like he is getting the flu; This is a spontaneous report from a contactable consumer. A 75-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2, by injection, administered in left arm on 20Apr2021 14:15 (Batch/Lot Number: EW0171) as single dose for covid-19 immunisation. Medical history were none. Concomitant medication(s) included atorvastatin (ATORVASTATIN) taking for several years at 20mg, once daily by mouth for blood cholesterol; lisinopril (LISINOPRIL), taking for a year; prior to that he took Atenolol, 50/25mg once daily; [withheld] vial at 5mg, one twice daily by mouth for blood pressure, all ongoing. Historical vaccine included first dose, BNT162B2 on 30Mar2021 between 14:15PM and 14:30PM in the left arm,Lot number EW0150 and experienced sore arm on 30Mar2021. The patient received the 2nd dose of the Pfizer covid vaccine yesterday, waken about 2am, feeling as if he has the flu, no fever, just blah feeling. Can he take Tylenol or Advil, just to feel a little better. He has some discomfort in the arm and is feeling like he has the flu but with no fever. The second shot he had a little soreness in the arm again but less than the first time. Adds that soreness is still there when he raises his arm and he can tell he had a needle in his arm. This morning when he awakened, about 16 hours after the shot, he felt like he was getting the flu, but it was just some discomfort. Adds he checked his temperature and he had no fever. No emergency room or physician office visit. Not vaccinated at Facility. Feeling like he is getting the flu was on 21Mar2021. Outcome was not recovered for all events. No follow-up attempts are needed. No further information is expected.

Other Meds: ATORVASTATIN; LISINOPRIL

Current Illness:

ID: 1305311
Sex: F
Age:
State: OH

Vax Date: 04/20/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: Migraine; This is a spontaneous report from a contactable Other HCP. A 59-year-old female patient (Other HCP) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE lot number: unknown, Expiry date: unknown) via an unspecified route of administration on 20Apr2021 for COVID-19 immunization. The medical history included focal migraines. Concomitant medications were not reported. In Apr2021, she was experiencing a migraine at the moment, but she's had migraines in the past, specifically focal migraines, for which light was the factor. When she gets them, she "can't see very well", everything was "just too bright. The second dose schedule is on 05May2021. The events were reported as non-serious. The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305312
Sex: F
Age:
State:

Vax Date: 04/20/2021
Onset Date:
Rec V Date: 05/11/2021
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: Eyes are dry and itchy, and also eyes are watering; Eyes are dry and itchy, and also eyes are watering; eyes are dry and itchy, and also eyes are watering; Eye pain; This is a spontaneous report from a contactable consumer. This consumer (patient) reported that a 40-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 20Apr2021 at single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. The patient experienced eyes were dry and itchy, and also eyes were watering. Patient stated that she googled it and read there was no treatment for eye pain, and also people got shingles after the COVID shot. Outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained

Other Meds:

Current Illness:

ID: 1305313
Sex: F
Age:
State:

Vax Date: 03/30/2021
Onset Date:
Rec V Date: 05/11/2021
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: a lot of muscle and joint pain; a lot of muscle and joint pain/sore in her hip joint; stiff neck and shoulders and shortly after it went to her lower back and legs and she couldn't bend over; stiff and sore in her hip joint and lower back; stiff and sore in her hip joint and lower back; This is a spontaneous report received from a non-contactable consumer(patient). This 75-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 30Mar2021 at single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. The patient got the first shot on 30Mar2021 and had been having a lot of muscle and joint pain. It started a couple of days after, she got a stiff neck and shoulders and shortly after it went to her lower back and legs and she couldn't bend over. It was still stiff and sore in her hip joint and lower back but she said it was somewhat maybe a little better. She is scheduled for the second shot tomorrow and is very hesitant. She asked how long this will last and if the second shot will make things worse. The outcome of events was unknown. No follow up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305314
Sex: M
Age:
State: CO

Vax Date: 04/15/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: Fever of 104; Sore throat; Chills; Symptoms like alergies; Cold like symptoms; This is a spontaneous report from a contactable consumer via Pfizer Sponsored Program. A 16-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection), via an unspecified route of administration on 15Apr2021 as a single dose for COVID-19 immunization. The patient's medical history and concomitant medication were not reported. The patient was fine until Sunday (Apr2021) then the patient had a fever of 104, sore throat, chills, and symptoms like allergies. The patient was treated with Tylenol and the fever broke but still having cold like symptoms. The reporter wants to know what should do now. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305315
Sex: F
Age:
State: NJ

Vax Date: 04/10/2021
Onset Date: 04/10/2021
Rec V Date: 05/11/2021
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: Blood pressure is now reading 170/80 and dropped a little to 140/90; This is a spontaneous report received from a contactable consumer (patient). A 61-years-old female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: ew0162), via an unspecified route of administration on 10Apr2021 as a single dose for COVID-19 immunization. The patient medical history and concomitant mediation was not reported. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: ep7534), via an unspecified route of administration on 20Mar2021 as a single dose for COVID-19 immunization and had no problems. The patient reported that for 10 years she gets up, she works out and checks her B/P which was usually 110/70, 110/60. Since the vaccination, the patient blood pressure was now reading 170/80 and dropped a little to 140/90 and it had never been that high and stated that sorry the patient got the vaccine. The patient was beside physician because the patient's blood pressure had never been so high. The clinical outcome of the event was unknown. No follow-up attempts are needed. No further information was expected.

Other Meds:

Current Illness:

ID: 1305316
Sex: F
Age:
State:

Vax Date: 04/19/2021
Onset Date: 04/20/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: the injection site under her bandage was red and swollen; the injection site under her bandage was red and swollen; This is a spontaneous report from a contactable consumer (patient) via Medical Information Team. A 50-year-old female patient received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: UNKNOWN) via unspecified route of administration on 19Apr2021 as single dose for COVID-19 immunization. Patient was 50-years-old at the vaccination. Patients medical history and concomitant medications were not reported. Yesterday (20Apr2021) morning around 8:40am-9am the injection site under her bandage was red and swollen. Today her arm was a little better, and the swelling has gone down a little bit. The outcome of the events injection site under her bandage was red was unknown and swollen was recovering/resolving. No follow-up attempts are needed. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305317
Sex: F
Age:
State:

Vax Date: 04/02/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
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: a rash, it is like blisters; a rash, it is like blisters; This is a spontaneous report received from a contactable consumer reported for self. This female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 02Apr2021 as single dose for covid-19 immunisation. Medical history was none. This week the patient noticed a rash, it is like blisters in Apr2021. 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: 1305318
Sex: F
Age:
State: CA

Vax Date: 04/17/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
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: This is a spontaneous report from a contactable consumer (patient). This female patient of unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) in the morning of 17Apr2021 as single dose for COVID-19 immunization. Medical history and concomitant medications were not provided. The patient got the first dose on 17Apr2021 morning, she was fine that day, although at night she had arm pain. The next day (18Apr2021), her arm pain continued and she felt very tired. In morning of 19Apr2021, she began having vertigo, she had it since 19Apr2021 until the reporting time, patient asked is it normal after the vaccine? Previously she had no vertigo. She got dizzy, she felt dizzy when she turned around on an unspecified date in Apr2021. Outcome of the event vertigo was not recovered, while other events was unknown. This report was assessed as non-serious. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305319
Sex: F
Age:
State: CA

Vax Date: 03/04/2021
Onset Date: 03/14/2021
Rec V Date: 05/11/2021
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: shingles; This is a spontaneous report from a contactable consumer. This consumer reported similar events for two patients. This is the first of two reports. A 103-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number, and expiration date not reported), via an unspecified route of administration, administered on the arm on 04Mar2021 at a single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient received her first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 09Feb2021 for COVID-19 immunisation. On 14Mar2021, patient experienced shingles (reported as approximately 7-10 days after vaccination). Therepeutic measurement was taken as a result of shingles included valacyclovir (VALTREX). The outcome of shingles was recovered on an unspecified date. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021443579 Same reporter, drug, and event; different patient

Other Meds:

Current Illness:

ID: 1305320
Sex: F
Age:
State: CA

Vax Date: 03/04/2021
Onset Date: 03/14/2021
Rec V Date: 05/11/2021
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: shingles; This is a spontaneous report from a contactable consumer or other non hcp. This consumer reported similar events for two patients. This is the 2nd of two reports. A 56-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number, and expiration date not reported), via an unspecified route of administration, administered on the arm on 04Mar2021 at a single dose for COVID-19 immunisation. The patient had no relevant medical history and patient's concomitant medications were not reported. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, batch/lot number, and expiration date not reported), via an unspecified route of administration on 09Feb2021 at a single dose for COVID-19 immunisation. Facility where the most recent COVID-19 vaccine was administered: Hospital. On 14Mar2021, patient experienced shingles (reported as approximately 7-10 days after vaccination). Patient resumed use of valacyclovir (VALTREX) as a result of the event. The outcome of shingles was recovered on an unspecified date. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021443578 Same reporter, drug, and event; different patient

Other Meds:

Current Illness:

ID: 1305321
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: developed an itchy trunk; rash radiated to arms; This is a spontaneous report from a contactable Pharmacist. This Pharmacist reported for a 74-year-old male patient that received first dose of BNT162B2 (BNT162B2, Pfizer-BioNTech Covid-19 Vaccine), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as single dose for Covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced/developed an itchy trunk and then rash radiated to arms on an unspecified date with outcome of unknown. She wants to know if he can receive the second dose of the vaccine in a retail setting. The pharmacist reported that "is itchiness of the trunk and arms a contraindication to the vaccine?" No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305322
Sex: F
Age:
State:

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
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: contracted shingles; This is a spontaneous report from a contactable consumer report for self. This 74-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient said she was due tomorrow for her second dose but she has contracted shingles this week (in Apr2021) and started on Valtrex medication for it 2 days ago. Event outcome was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305323
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
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: arm hurt; headache; This is a spontaneous report from a non-contactable consumer. A male patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced arm hurt and headache on an unspecified date. Reported as: Upon callback, caller's mother stated, "Your shot is wonderful. My whole generation got it; my brother in law, sister in law, everybody took it. They got a light headache and their arm hurt, but it was not bad. We loved it. My husband is fine. My husband feels stronger now than anything." The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305324
Sex: M
Age:
State:

Vax Date: 04/17/2021
Onset Date: 04/18/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: lost the sense of smell and taste; Lost the sense of smell and taste; I have trouble breathing; Chills; Fever; body aches/pain; Sore throat; very weak; felt really bad/not feeling well; This is a spontaneous report from a contactable consumer (patient). This male patient of unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 17Apr2021 as single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not provided. On Saturday 17Apr2021, patient received the first dose of the COVID-19 vaccine from Pfizer. On Sunday (18Apr2021), he was not feeling well and felt really bad. On Monday (19Apr2021), he had chills, fever, body aches/pain, sore throat, he felt very bad, very weak. Today (21Apr2021), patient woke up feeling better, but about an hour ago he felt like he had lost the sense of smell and taste, and he had trouble breathing. On 21Apr2021, patient felt great, but now he had lunch and lost his sense of smell and taste. On Friday 16Apr2021 (1 day before receiving the vaccine), he got tested to see if he was infected with COVID-19 and it came back negative, 10 days ago he also had a test and it was negative, so he claimed that he did not have COVID and these symptoms should be because of the vaccine. Lab data included COVID-19 with result of negative on unspecified date and on 16Apr2021. 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: 1305325
Sex: F
Age:
State: MN

Vax Date: 04/20/2021
Onset Date:
Rec V Date: 05/11/2021
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: he is feeling nauseous. everything wants to come out; thirsty; she cannot eat; she has a headache from hell; she didn't get a wink of sleep; does not feel good; This is a spontaneous report from a contactable consumer (patient). A 62-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number and expiry date unknown), via an unspecified route of administration on 20Apr2021 as a SINGLE DOSE for COVID-19 immunisation. Medical history and concomitant medications were not reported. About 1 hour after the vaccine, the patient developed side effects. Caller stated she has a headache from hell, she can not eat and everything wants to come out. Caller stated this does not feel good stating she feels bad. Caller wanted to know what she can do. Caller stated got the 1st dose of the vaccine yesterday, April 20 and she is calling to report that she is feeling nauseous, thirsty and cannot eat. Caller wants to know if when she can feel like a normal person again. Patient reported that she will be 63 in about a week. The caller stated that she got the first shot yesterday and all was fine on the way home but when she was home her head was pounding. She has a headache the size of the Mississippi river and she didn't get a wink of sleep. She said the headache is so horrible. She asked when this will go away. Outcome of the events were not reported. No follow-up attempts are Possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305326
Sex: F
Age:
State: NJ

Vax Date: 04/20/2021
Onset Date: 04/20/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: her baby's pediatrician told her the patient could pass antibodies to the baby through breastfeeding; her baby's pediatrician told her the patient could pass antibodies to the baby through breastfeeding; headache; light sensitivity; vision changed; extreme fatigue /Exhaustion; overall body aches; sweaty /Sweating Profusely; her pupils were dilating and constricting; her pupils were dilating and constricting; Brain Fog; This is a spontaneous report received from a contactable consumer (patient). The consumer reported information for both mother and baby. This is the maternal report. A 36-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 20Apr2021 at age of 36 years at single dose for COVID-19 immunisation. Medical history included ongoing asthma, had basically had all of her life; since she was about 8 years old. Her grandfather had strokes. Her father died of a heart attack. Patient had no concomitant medications. Patient received her first Pfizer Covid vaccine dose on 20Apr2021. She stated that after the vaccine was administered (on 20Apr2021), she started to experience extreme fatigue and needed to sleep. After waking up from a nap, she noticed vision changed, headache with light sensitivity, overall body aches, and sweaty. Her husband told her that her pupils were dilating and constricting. Her MD advised her to go to the ED. Patient stated why the patient taking covid vaccination was asthma, medical worker and having a 9-month-old baby. Patient stated that she had been experiencing vision problems and a severe headache. Said her pupils had been dilating and contracting. Patient had severe headache, vision problems; pupils keep dilating and contracting, exhaustion, brain fog, sweating profusely on 20Apr2021. Said her symptoms started yesterday 20Apr2021, stopped, and then started again today. Stated she had questions about her side effects and asked should she go the Emergency Room; especially for the headache. Said today they were just as bad as yesterday; except she was not as exhausted today as she was yesterday. Patient stated that her main reason was because her baby's pediatrician told her the patient could pass antibodies to the baby through breastfeeding. Patient denied any medications, labs, testing, or treatments relevant to report. AE(s) did not require a visit to Emergency Room and Physician Office. Patient stated no adverse events after prior vaccinations; only an antibiotic. Outcome of exhaustion was recovering and the other events was not recovered. No follow-up attempts are needed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021446591 Same reporter/drug, different patient/event (baby case)

Other Meds:

Current Illness: Asthma

ID: 1305327
Sex: F
Age:
State:

Vax Date:
Onset Date: 04/16/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: This is a spontaneous report from a contactable pharmacist via the medical information team. A 48-year-old female patient received bnt162b2 (COVID-19 VACCINE), dose 1 intramuscular on an unspecified date (Batch/Lot number was not reported) as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On 16Apr2021, the patient experienced severe vomiting and nausea. On an unspecified date, it got so bad over the next day or two, she couldn't eat started vomiting, and had to go to the Emergency Room where she didn't know if she was treated with medication. They could not find anything wrong with her gallbladder or pancreas. That lasted from Friday and not abiding - thought it may be a reaction from the COVID-19 vaccine. She needed someone to drive her home, they took her back to ER and gave her a new anti-nausea, but she still hasn't been able to eat food yet. On an unspecified date, the patient experienced slight stomach ache, throwing up, violently ill, able to limp home, very weak, could not lift her head off the pillow, and could not lift her head up. On 20Apr2021, she didn't seem to have symptoms, no fever or anything, that she had a UTI. They performed a CT which showed inflammation in the stomach, and maybe the gallbladder was a little irritated too. The patient underwent lab test and procedure which included ultrasound: gallbladder and pancreas normal on 18Apr2021 and Gallbladder had no stones/no pathology on 20Apr2021. The patient underwent CT scan with inflammation in the stomach and urine test with UTI on 20Apr2021. 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: 1305328
Sex: F
Age:
State:

Vax Date: 04/15/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
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: sore arm; sore neck/ neck pain; sore throat; headache; nausea; vomiting (threw up twice); joint pain; could not move her arm for 6 days; This is a spontaneous report from a contactable consumer (patient) via Pfizer sponsored program. A female patient of an unspecified age received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number- UNKNOWN) via an unspecified route of administration on 15Apr2021 as single dose and had previously received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number-UNKNOWN) via an unspecified route of administration on 16Mar2021 as single dose for covid-19 immunization. Patient medical history included COVID from an unspecified date in Jan2021 and dizziness from an unspecified date in Jan2021 which went away after five days of first dose and concomitant medications were not reported. Patient did not get tested for COVID-19. Patient said after first dose of the covid-19 vaccine she had a really sore arm, her second dose was last Thursday (15Apr2021) had a sore arm, sore neck/neck pain, sore throat, headache and nausea that lasted over 5 days, vomiting (threw up twice) could not move her arm for 6 days and joint pain and stated she had symptoms for 6 days after the second dose. Caller asked is it usual to have symptoms for six days. Caller asked if you have antibodies from having covid, can you have a stronger response to the second dose and have more side effects. Caller stated a doctor on TV had covid and was sick for 6 to 7 days after his vaccine. She read an article from a provider about people with Rh negative factor and O negative blood had very mild symptoms of covid-19 and would like to speak to someone, relayed PMI number and hours, she had to go but will call number given, caller disconnected, will fax AE. The outcome of the events was unknown. Upon follow-up (21Apr2021): This is a follow up spontaneous report from a female contactable consumer. This female consumer (patient) reported. Upon follow-up (23Apr2021): This is a follow up spontaneous report from a female contactable consumer. This female consumer (patient) reported that: Only adverse event present and no PQC present. Upon follow-up (21Apr2021): This is a follow up spontaneous report from a female contactable consumer. This female consumer (patient) reported about relevant medical history which was captured above and in the relevant fields. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305329
Sex: F
Age:
State: TX

Vax Date: 04/21/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
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: a rash "shaped like 25 cents" which burns, on her left arm, surrounding where she received the vaccine/ got a rash on her skin that started to burn; a rash "shaped like 25 cents" which burns, on her left arm, surrounding where she received the vaccine/ got a rash on her skin that started to burn; This is a spontaneous report from a contactable consumer. A 41-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on 21Apr2021 09:11 (Batch/Lot number was not reported) as single dose at left arm for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient experienced after she left, she developed a rash "shaped like 25 cents" which burns, on her left arm, surrounding where she received the vaccine. She's got a rash on her skin that started to burn. Outcome of events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305330
Sex: M
Age:
State: CA

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
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: tingling of feet and face; He had his Inflectra infusion, three days after his first shot of the Pfizer COVID19 vaccine; Stated that his cal protectnin number jumped up after he got the vaccine; This is a spontaneous report received from a contactable reporter. A 16-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: solution for injection, Lot number and expiration date not reported), via an unspecified route of administration on an unspecified date, as a single dose for COVID-19 immunization. Medical history included cal protectnin. Concomitant medications were not reported. Caller was calling for her son that is also on Inflectra. He got his first dose of the Pfizer BioNTech COVID19 vaccine. He had his Inflectra infusion, three days after his first shot of the Pfizer COVID19 vaccine. He has his second dose on Friday, and she is wondering if it is safe to get his second dose at 21 days or if he should wait longer. It seems that she is asking if there was an interaction. She later mentions that after his first dose of the COVID19 vaccine he had a reaction: tingling of feet and face. Caller states that she was very frustrated with us. She feels like we're not providing her with the information she needs, and she has to make a tough decision for her child. Both are our medicines (Inflectra and Pfizer COVID19 vaccine) and we should have this information. Patient that stated that her son had Pfizer Vaccine for Covid earlier in the month and three days after had an Inflectra infusion. Stated that he is coming up for an appointment for another Inflectra infusion which is 3 weeks later. Wanted to know if he should get the vaccine again and if it was too much in a given time frame. Clarified that his infusions are eight weeks apart. Stated that the pharmacy told her that he was to not take any other medication with the Inflectra which made her hesitant. Stated that they did the vaccine and was told by the doctor it was okay. Wanted to know how long to wait between first and second vaccine knowing he had an infusion three weeks after it. Wanted to know if it was 42 days in-between. Stated that his cal protectnin number has been going down since October. Stated that his cal protectnin number jumped up after he got the vaccine. Stated that it was not greater than 8000 and has gradually decreased. Wanted to know if they should wait longer for second for the second vaccine to make sure that it was not messing with his Inflectra. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: INFLECTRA

Current Illness:

ID: 1305331
Sex: M
Age:
State:

Vax Date: 04/19/2021
Onset Date: 04/20/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: blurry eyes; Headache; numb face and arms; Felt dizzy; Had to call out of work to rest and sleep all day; This is a spontaneous report from a contactable consumer (patient) from a Pfizer sponsored program. A 52-year-old male patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot number: UNKNOWN) via an unspecified route of administration on 19Apr2021 16:00 as single dose for COVID-19 immunization. The patient's medical history included diabetes. Concomitant medication was not reported. The patient received second dose of Pfizer BioNTech Covid 19 vaccine on Monday 19Apr2021 around 4pm. The next day the patient experienced numb face and arms, felt dizzy, and had to call out of work to rest and sleep all day. Today he felt okay but started feeling dizzy with a headache and blurry eyes. He has diabetes but has been taking his blood sugar in the morning and they have been okay. He has been taking tylenol for the headaches. The patient said he was driving to work next day and face and arm went numb. Had to turn around and go back home. Next day tried going to work again, face and arm went numb also was dizzy and slight headache. Wants to know if this side effect has been reported and what do we suggest. It was reported that the patient went to see his animals and I (sentence incomplete). I am calling you because of the side effects that I am having from the vaccine. Also, I want to know if this was the part of the side effects that was going on with me. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305332
Sex: F
Age:
State: AZ

Vax Date: 04/07/2021
Onset Date: 04/07/2021
Rec V Date: 05/11/2021
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: blood did not flow (suspecting that she had problems with blood clotting)/blood clotted when she cut her finger; got a cut above her finger.; developed a big bruise/bruise on her foot above the knee, on the back of the leg/it was like the size of her hand/Bruise on right leg; It was like she had sand in her eyes; tired; dryness in her eyes; eyes hurt; fast heartbeat; headaches; This is a spontaneous report from a contactable consumer (patient). A 57-years-old female patient received the first dose bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE), via an unspecified route of administration, administered in Arm Left on 07Apr2021 at 11:30 (at the age of 57 years old) (Batch/Lot Number: EW0153; Expiration Date: 31Jul2021) as SINGLE DOSE for covid-19 immunization . Medical history included Allergies. There were no concomitant medications. The patient experienced got a cut on her finger and blood did not flow (suspecting that she had problems with blood clotting)/blood clotted when she cut her finger, developed a big bruise/bruise on her foot above the knee, on the back of the leg/it was like the size of her hand/bruise on right leg, it was like she had sand in her eyes, tired; on 07Apr2021 experienced headaches; On 08Apr2021 dryness in her eyes and eyes hurt and fast heartbeat. The adverse event did not require a Physician office visit or emergency room visit. No other vaccines were given within 4 weeks. Patient has not had a vaccine in 8 to 10 years. The patient underwent lab tests and procedures which included heart rate: fast on an unspecified date. The clinical course was reported as follows Consumer reported side effects that she had experienced post-administration of the first dose of the PFIZER-BIONTECH COVID-19 VACCINE. She developed a big bruise. The bruise was on her foot above the knee, on the back of the leg. It was like a 15 inch big bruise, clarified it was like the size of her hand. Patient got a cut above her finger. The blood did not flow, it just clotted, (suspecting that she had problems with blood clotting) that had never happened to her before. She called a doctor who said she needed to have a blood test to see if she has clotting before taking the second dose. Patient also had experienced a fast heartbeat. The fast heartbeat was really bad. It began right after the vaccine, clarified as the next day. She had a fast heartbeat for like 10 days. She didn't think that the fast heartbeat had anything to do with vaccine, she thought maybe it was because she did not drink a lot of water. The patient had headaches the first 3 days and was tired the first few days. She believes her headaches started the evening of the same day as the vaccine. For the first 3 days it was continuous. Since then, it has been off and on. Did not take medication. The headache was there but it wasn't like she couldn't move because of it. She had dry eyes and her eyes hurt. It was like she had sand in her eyes. She would rub them because it felt like something was in them. She would wash her face and eyes and it was still there. The first day she was busy all day and didn't go anywhere after receiving the vaccine. She didn't feel this symptom until the next day when she went out. She didn't think much of it because of allergies and was going in and out. But, when her friend said she had the same symptoms she figured out it was because of the vaccine. She confirms her eyes are still dry but didn't hurt like it did the first few days. She confirms it has gotten better. She wanted to know if she can proceed in getting the second dose given side effects experienced or if she would also need to have a blood test to determine the problems with clotting earlier and mentioned she does not have an appointment for the second dose. The clinical outcome of the event eye hurt, ,dryness in eyes was recovering while the remaining events was unknown.

Other Meds:

Current Illness:

ID: 1305333
Sex: F
Age:
State:

Vax Date: 04/07/2021
Onset Date:
Rec V Date: 05/11/2021
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: arm soreness; weird lymph node pain all over her body; weird muscle or nerve pain in her legs; weird muscle or nerve pain in her legs; skin hurts all over; Her groin lymph nodes and lymph nodes in her neck were really painful; This is a spontaneous report from a contactable consumer (patient's mother). This consumer reported for her 36-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection) via unspecified route of administration on 07Apr2021 as SINGLE DOSE for COVID-19 immunization. The medical history and concomitant medication were not reported. Approximately on unknown date in 2021, about a week in patient had arm soreness and she's been having weird lymph node pain all over her body. Her groin lymph nodes and lymph nodes in her neck were really painful. It started with weird muscle or nerve pain in her legs. She has gone to her doctor and they don't know what to do. On an unknown date in 2021, the patient performed with a blood test and x-ray, but the results are not provided. Her skin hurts all over. We're not sure what it is, but I'm concerned about her getting her 2nd vaccine. Patient mother asking, the skin pain is a symptom of lymphadenopathy. Patient mother asking what the protocol for managing these side effects. Patient mother also enquired about lymphadenopathy would be worse after the second dose. The caller also asked about the efficacy of the first shot. The response included, https://www.pfizer.com/news/press-release/press-release-detail/pfizer-and-biontech-announce-publication-results-landmark.The cumulative incidence of COVID-19 cases over time among placebo and vaccine recipients began to diverge by 12 days after the first dose, and 52.4% vaccine efficacy (95% confidence interval: 29.5, 68.4) was observed between dose 1 and dose 2, indicating the early onset of a partially protective effect of immunization. Two doses of vaccine provide the maximum protection observed. The outcome of the events was unknown. No PQC involved. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305334
Sex: F
Age:
State: CA

Vax Date: 04/13/2021
Onset Date:
Rec V Date: 05/11/2021
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: went in for her second dose on Tuesday she also got shingles; This is a spontaneous report from a contactable other healthcare professional. This other healthcare professional reported same events for two patients (patient himself and his mom). This is the second of two reports. A 78-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) (at 78 years of age), via an unspecified route of administration, administered in arm right on 13Apr2021 (Batch/Lot Number: ER8729) as 2nd dose, single for COVID-19 immunisation. The patient's medical history was not reported. There were no concomitant medications. Historical vaccine included BNT162B2 dose 1 on 22Mar2021 (lot number: EN6208) (at 78 years of age) for COVID-19 immunisation. The patient went in for her second dose on Tuesday, she also got shingles. It was mentioned that the patient recently got diagnosed today (unspecified) so she was not taking anything currently but she takes some antiviral (not sure exactly what it was). It was clarified that the patient had not yet taken treatment for the event but the reporting other healthcare professional was sure that she will be. The outcome of the event was unknown.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021381912 same reporter/drugs/events; different patients

Other Meds:

Current Illness:

ID: 1305335
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
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: redness and itchy at injection site arm; redness and itchy at injection site arm/it itches; This is a spontaneous report from a contactable consumer (mother-in law of patient) or other non-health care professional. A 94-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as SINGLE DOSE for covid-19 immunization. The patient medical history, concomitant medications were not reported. On an unspecified date patient experienced redness and itchy at injection site arm (vaccination site erythema), redness and itchy at injection site arm/it itches (vaccination site pruritus). The outcome of events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305336
Sex: F
Age:
State: HI

Vax Date: 04/10/2021
Onset Date: 04/12/2021
Rec V Date: 05/11/2021
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: intestinal upset; blood in nose mucous; Headache/low grade headache; dizziness; sinus stinging; runny nose; diarrhea; numbness in fingers; tiredness; weakness; This is a spontaneous report from a contactable consumer (the patient). A 61-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, lot number not provided), via an unspecified route of administration in the left arm on 10Apr2021 13:15 (at the age of 61-years-old) as a single dose for COVID-19 immunization. The patient had no medical history. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient was not pregnant at the time of vaccination. Concomitant medication included azithromycin. The patient previously took and had known allergies to Sulphur. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 12Apr2021, the patient experienced the following events: headache for 2 days, dizziness, then low grade headache for 1 week, sinus stinging and runny nose, blood in nose mucous, diarrhea for 1 week, intestinal upset, numbness in fingers, and overall tiredness and weakness for over one week. No treatment was received for the events. The outcome of the events was recovered in Apr2021. It was also reported that since the vaccination, the patient had not been tested for COVID-19. Information about the Lot/batch number has been requested.

Other Meds: AZITHROMYCIN

Current Illness:

ID: 1305337
Sex: F
Age:
State:

Vax Date: 04/16/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
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: fever; chills; fatigue; pain; This is a spontaneous report received from a contactable consumer. A 57-year-old female patient received first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection; Lot Number: Unknown), from an unspecified route and location on 16Apr2021 as SINGLE DOSE for covid-19 immunization. The patient's medical history and concomitant products were not reported. The patient experienced fever, chills, fatigue, and pain on Apr2021. The patient wanted to know how symptoms may be with the second Pfizer Covid 19 Vaccine?. The clinical outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305338
Sex: F
Age:
State:

Vax Date: 03/01/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: Horrific migraines; metallic taste following dose; This is a spontaneous report from a contactable consumer. A 36-year-old female patient received BNT162B2 second dose on unspecified date about a month ago (Mar2021) at single dose for Covid-19 immunization. Medical history and concomitant medications were not reported. Historical vaccine included BNT162B2 first dose on unspecified date for Covid-19 immunization. Patient had Horrific migraines. Reports no history of migraines. Exhibited four days ago. Also indicates metallic taste following dose. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305339
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
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: felt like the sensation that it was running through body; through legs, arms, chest/ mainly a sensation in legs, traveling from the top of legs down to feet/ No pain/ didn't last very long; This is spontaneous report from a non-contactable consumer (patient). A male patient of unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number and expiration date unknown) via an unspecified route of administration on an unspecified date (unknown age at time of vaccination), at single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient stated he received the Pfizer COVID vaccine and had a side effect. Patient stated when he received his first dose, he felt like the sensation that it was running through his body; through his legs, his arms, his chest. There was mainly a sensation in his legs, traveling from the top of his legs down to his feet. No pain, it just felt like it was moving through his body and it didn't last very long. Patient asking if this is a common side effect. 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: 1305340
Sex: F
Age:
State:

Vax Date: 04/01/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
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: Felt really strange; My body kept heating up, heating up, and heating up and then I got a headache; My body kept heating up, heating up, and heating up and then I got a headache; This is a spontaneous report received from a contactable consumer (patient). A 57-year-old patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) in Apr2021 at single dose for COVID-19 immunization. Medical history and concomitant medication were not reported. patient received her first shot on Sunday afternoon and when she was there the first 3 minutes, she felt really strange and her body kept heating up, heating up, and heating up and then she got a headache. Patient asked if that was a side effect or if it was normal. It lasted anywhere from 8-10 minutes. Patient asked If she decide not the get the second shot will the first shot protect her. patient asked "I wouldn't die, would I?" patient was recovered from the events in Apr2021. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305341
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
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: feeling discomfort and pain in the arm where he had the shot; feeling discomfort and pain in the arm where he had the shot; This is a spontaneous report from a contactable consumer or other non hcp (Patient). A 44-years-old male patient received bnt162b2 (BNT162B2), dose 1 at 11:37 am via an unspecified route of administration and unspecified date (Batch/Lot number was not reported) as single dose for covid-19 immunisation. Second dose was scheduled for 12May2021. The patient medical history and concomitant was not reported. On an unspecified date, after first dose he started feeling discomfort and pain in the arm where he had the shot, and took 2 Tylenol at 2:45 pm. The outcome of the events was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained

Other Meds:

Current Illness:

ID: 1305342
Sex: F
Age:
State: NC

Vax Date: 01/25/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: Fever; HEADACHE; 8 days after 1st vaccination itchness and redness in app 3/4 diameter around injection site; Redness at the injection site with a diameter of 3/4 inch; This is a spontaneous report from a contactable consumer or other non hcp. A female patient of an unspecified age received first dose of bnt162b2 (BNT162B2, formulation: solution for injection, Batch/Lot Number: EL3247), via an unspecified route of administration, administered in Arm Left on 25Jan2021 14:00 as SINGLE DOSE for covid-19 immunisation. Medical history included drug hypersensitivity from 1975 to an unknown date and obesity from 1995 to an unknown date. The patient's concomitant medications were not reported. The patient experienced fever, headache, 8 days after 1st vaccination itchness and redness in app 3/4 diameter around injection site, redness at the injection site with a diameter of 3/4 inch. The patient underwent lab tests and procedures which included body temperature: 102. It was reported that no available reaction after body aches and fever (102) that stated 12 hour after the second acceration. The patient added that her daughter and lets that had similar reaction her husband had moderna, they tool 2 doses of Lylanol for the fever and felt fine by 48 hours after the second acculation. Therapeutic measures were taken as a result of fever took Lylanol as treatment received. The outcome of event was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305343
Sex: F
Age:
State: NY

Vax Date: 03/26/2021
Onset Date: 03/26/2021
Rec V Date: 05/11/2021
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: felt faintness; a quick electric shock across top of head; momentary faintness; having trouble swallowing/uncomfortable to swallow; throat felt sore; Throat remained irritated; mild discomfort in her shoulder; stuffy ears; This is a spontaneous report from a Pfizer-sponsored program by a contactable consumer (patient). This 58-year-old non-pregnant female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in left arm on 26Mar2021 12:45 (Lot Number: EN6205) as single dose for COVID-19 immunisation. Medical history included hypertension, asthma, chronic obstructive pulmonary disease (COPD), allergies: Penicillin, environmental allergies. Concomitant medications included lisinopril; montelukast sodium (SINGULAIR); cetirizine hydrochloride (ZYRTEC ALLERGY); bupropion; fluticasone propionate, salmeterol xinafoate (ADVAIR); prednisolone (SPIRICORT). On 26Mar2021 13:00, the patient experienced felt faintness, a quick electric shock across top of head, momentary faintness, having trouble swallowing/uncomfortable to swallow, throat felt sore, throat remained irritated, mild discomfort in her shoulder, stuffy ears. No treatment required for the events. The outcome of the event felt faintness was recovered and the outcome for the other events was unknown. The clinical course was reported as follows: She received her first Pfizer Covid vaccine on 26Mar2021. Within a few minutes, she felt faintness and had difficulty swallowing. She stayed for 30 minutes, it didn't go away but it didn't get worse and she left and went home. She a reports a history of allergies, asthma, COPD. She reports that she did not have compromised breathing. She states she could eat or drink but had a perpetual feeling of difficulty swallowing. She also had mild discomfort in her shoulder, sore throat, and stuffy ears. She reports her difficulty swallowing went away after 10 hours. She took Zyrtex, Singulair, and 3 different inhalers before the vaccine. She is wondering if it is possible that these medications blunted an anaphylactic reaction? Her MD gave her an epipen to take with her for her second dose. She takes lisinopril also.

Other Meds: LISINOPRIL; SINGULAIR; ZYRTEC ALLERGY; BUPROPION; ADVAIR; SPIRICORT

Current Illness:

ID: 1305344
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
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: Itching and red spots on the hands; Itching and red spots on the hands; Bump under the lips; Hard time swallowing; Skipping steps/ balance issue; This is a spontaneous report from a contactable consumer (patient). A 62-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number and expiration date unknown) via an unspecified route of administration on an unspecified date (62-year-old at time of vaccination), at single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. Patient experienced a bad reaction, itching and red spots on the hands, bump under the lips, hard time swallowing, skipping steps/ balance issue. Patient wanted to know should she get the second dose or not. 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: 1305345
Sex: F
Age:
State:

Vax Date: 04/16/2021
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
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: I started experiencing hives and itchy welts; This is a spontaneous report from a non-contactable consumer (patient) reported for herself. A female patient of unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 16Apr2021 at single dose for COVID-19 immunization. Medical history and concomitant medication were not reported. Patient had the first dose of the Pfizer covid 19 vaccine on 16Apr2021, Friday at noon. Late last night (Apr2021) she started experiencing hives and itchy welts. Reporter asked if it was okay to take an antihistamine. Patient asked if she had a side effect after the first dose of the vaccine. If she should get the second dose. Reporter asked if it was this a common side effect. 09May2021, scheduled for second dose. 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: 1305346
Sex: F
Age:
State: CA

Vax Date: 04/13/2021
Onset Date: 04/18/2021
Rec V Date: 05/11/2021
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: fatigue; sinus and chest congestion; sinus and chest congestion; This is a spontaneous report received from a contactable consumer (patient) via Pfizer sponsored program. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number and Expiration date: not reported), dose 1 via an unspecified route of administration on 13Apr2021 as 1st dose, single for COVID-19 immunisation. The patient medical history included COVID-19 from Jan2020 to an unknown date (she had the corona virus in Jan2020, she tested positive then). The patient's concomitant medications were not reported. On 18Apr2021, the patient experienced fatigue, sinus and chest congestion. On an unknown date, the patient underwent a COVID test, but results were still pending. The patient asked if that could be side effects to vaccine. Her second vaccine was due for May2021. The outcome of the events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305347
Sex: F
Age:
State: NC

Vax Date: 04/10/2021
Onset Date: 04/17/2021
Rec V Date: 05/11/2021
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: Headache; Back Pain; muscular weariness; Tired eyes; feel strange as sick; This is a spontaneous report from a contactable consumer (patient). A 37-year-old female patient (Pregnant: No) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in left arm on 10Apr2021 at 08:45 AM (lot number: EW0150) at single dose for COVID-19 immunization. The relevant medical history was reported as none. Concomitant medications were not reported. On 17Apr2021 at 17:00, the patient had headache, back pain, muscular weariness, tired eyes. She felt strange as sick. It's been almost two weeks since she got the vaccine but only on Saturday she started with a headache. When she empused herself she was in pain head for two days but they became all the symptoms together a week after. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The events were reported as non-serious. Therapeutic measures were taken as a result of the events. The outcome of the events was not recovered. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305348
Sex: F
Age:
State:

Vax Date:
Onset Date: 04/01/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: got the fever today; chills in the morning; This is a spontaneous report from a contactable consumer (reported for herself) via medical information team. A 38-year-old-female patient received first dose of BNT162B2 (Pfizer covid-19 vaccine, solution for injection, Lot number and Expiration date: Not reported) via an unspecified route of administration as a single dose on an unknown date, for Covid-19 immunization. Medical history and concomitant medications were not reported. On 21Apr2021 (the day of this report), she experienced fever. She had the chills in the morning. It was stated that she had like a 100.4 degree F and recently when she checked out it was 100.6 degree F. The outcome of the events of fever and chills unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305349
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: headache since taking the second dose of the Pfizer Covid vaccine; This is a spontaneous report from a contactable consumer (patient) reported for himself. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) at single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously received the first dose of bnt162b2 on an unspecified date for covid-19 immunization. Patient had a headache since taking the second dose of the Pfizer Covid vaccine and wanted to know if he could take Tylenol or Ibuprofen, he read somewhere that he was not supposed to take one them. The outcome of the event was unknown. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305350
Sex: M
Age:
State: FL

Vax Date: 04/14/2021
Onset Date: 04/14/2021
Rec V Date: 05/11/2021
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: has reflux, gas and bloating/gas and acid reflux is worse; has reflux, gas and bloating/gas and acid reflux is worse; has reflux, gas and bloating; he is so tired; hard time breathing from gas/ had a hard time breathing last night; hives on his face on both sides of his cheeks; disturbance on his throat; felt like something was blocking his throat; This is the spontaneous report from a contactable consumer (patient wife). A 63-year-old male (patient) received BNT162B2 (lot number: EW0158) first dose on 14Apr2021 16 15 PM on left arm at single dose for COVID-19 immunisation. Medical history included allergic to milk and beef, gives him hives on his face. Concomitant medications included nasal spray (he doesn't take any other medication). No Prior Vaccinations (within 4 weeks). Consumer asked if her husband can take benadryl before the vaccine. Consumer stated her husband has no known allergies to medications. Caller stated that her husband had the first dose of the Pfizer covid 19 vaccine on 14Apr2021 at about 4:00 pm. Caller stated he ate dinner and then around 8;00 or 8:30 he felt like a disturbance on his throat. Caller stated he could swallow but felt like something was blocking his throat. Caller stated that 1/2 hour later it went away. Caller reported the next day (15Apr2021) he had hives on his face on both sides of his cheeks. He is so tired. Caller stated her husband has reflux, gas and bloating. Hard time breathing from gas. Caller stated her husband had a hard time breathing from gas last night (20Apr2021). Gas and acid reflux is worse on 20Apr2021. Vaccine Administered at Military Facility was no. No event require a visit to: Emergency Room or physician office. The outcome of event disturbance on his throat was recovered on 14Apr2021, hives on his face on both sides of his cheeks recovered on 15Apr2021, gas and acid reflux is worse recovered on 21Apr2021, hard time breathing from gas/ had a hard time breathing last night was recovered on 21Apr2021. The outcome of other event was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305351
Sex: F
Age:
State: MI

Vax Date: 04/20/2021
Onset Date:
Rec V Date: 05/11/2021
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 weak and dizzy; dizzy; extremely dizzy I thought I was going to faint; I thought I was going to pass out; pulse get very low it got so slow; I felt really bad; This is a spontaneous report from a contactable consumer (patient). A 62-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EW0150, expiration date: 31Jul2021), via unspecified route of administration on 20Apr2021 at single dose for COVID-19 immunisation. The relevant medical history included allergies to preservatives, additives, soy, corn starch, anything, even olive oil; immune system was compromised; blood clot. Concomitant medications included warfarin sodium for blood clot. The patient received first dose of Pfizer COVID-19 vaccine and was very weak and dizzy, she got dizzy for 10 minutes and decided to stay there an additional 30 minutes, just sat there and got better, like her pulse got really really low, she felt it in her neck, very slow. Second dose is scheduled for 11May2021. The decision to receive the second dose for any other reason cannot be made. The patient was referred to speak to her healthcare provider about the risks of the vaccine compared to the risks of potentially not being fully protected against COVID-19 infection. Consumer stated she had vaccine first dose yesterday and she asked them for the paper work because she did have allergies 10 years ago and she now realize from reading the list here of the reaction that she did have reaction to the vaccine. The patient stated that the adverse event was not persisting, it was within the first 10 minutes and she stayed there for an hour because she was scared but it went away. Well the reaction she had was that she got extremely dizzy, she thought she was going to faint, that's the reaction she had after the vaccine. She thought she was going to pass out, and she saw her pulse get very low it got so slow. It was not just a quick feeling she felt really bad for 10 minutes. The patient underwent blood test with unknown results on an unspecified date. The outcome of the events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds: WARFARIN SODIUM

Current Illness:

ID: 1305352
Sex: M
Age:
State: MO

Vax Date: 01/26/2021
Onset Date: 01/26/2021
Rec V Date: 05/11/2021
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: Sore shoulder; Pain at injection site; This is a spontaneous report from a contactable consumer (patient). This consumer reported 2 reports for same patient and different dose, this is the second of 2 reports. A 43-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via intramuscular, administered in right arm (reported as right shoulder) on 26Jan2021 15:30 (Batch/Lot Number: EN5318; Expiration Date: 31May2021) as SINGLE DOSE for covid-19 immunisation at Workplace clinical. Patient's medical history reported as none. No prior vaccinations. No concomitant drugs. There were no concomitant medications. The patient experienced pain at injection site (seriousness criteria: not serious) on 26Jan2021 15:30 with outcome of recovered on an unspecified date, this event did not require the initiation of new medication/ other treatment/ procedure, sore shoulder on an unspecified date with outcome of unknown. No relevant test. First Dose resulted in a sore shoulder. No follow-up attempts are needed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021169816 Same patient, same product, different dose, similar events.

Other Meds:

Current Illness:

ID: 1305353
Sex: M
Age:
State: CA

Vax Date: 03/28/2021
Onset Date: 03/29/2021
Rec V Date: 05/11/2021
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: Hives; His body was red; Allergic reaction to Covid vaccine ingredient; This is a spontaneous report from a contactable consumer(patient's mother). A 23-year-old male patient received BNT162B2(PFIZER-BIONTECH COVID-19 VACCINE), dose 1 intramuscular, administered in Arm Left on 28Mar2021 (Lot Number: ER8732) as single dose for covid-19 immunization. The patient's medical history and concomitant medications reported as none. On 29Mar2021, the patient had an allergic reaction to the first vaccination of the Covid vaccine Pfizer (Couple of hours after), he broke out with hives, his body was red, so he went to an allergist, they did confirm that he was allergic to one of those ingredient (Covid vaccine) and allergist said he should not get his second vaccine, so he was not able to do that (second vaccine). No doctor prescribed the vaccine, he just found it online. Events lasted 2-4 days. He was recovered at the time of the report but he was scheduled to get his second shot this but the allergist told him, he should not get the second shot. The patient did an allergy test determined to see he was allergic to ingredient of Pfizer vaccine, just one test two days before. The patient had not taken any treatment for the allergy (event). The outcome of the events was recovered. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305354
Sex: F
Age:
State: TN

Vax Date: 03/22/2021
Onset Date: 04/04/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

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

Symptoms: Sore arms; Some heart palpitations; Very sensitive to light one side of head; chills; felt like she has been hit by a truck. It liked knock her out.; Headache on one side of head/ serious headache; Feel a lot of pressure on one side of head; This is a spontaneous report received from a contactable consumer (patient). A 49-year-old female patient received 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, LOT number: EL9261, expiration date unknown) on 22Mar2021 at age of 49-year-old via an unspecified route of administration on the left arm at single dose for COVID-19 immunisation. Patient previously received 1st dose of BNT162B2 (Lot number: EL9266) via an unspecified route of administration on the left arm on 25Feb2021 at age of 49-year-old at a school for COVID-19 immunisation. Medical history and concomitant medication was reported as no. The patient stated she was not sure if someone else has been reported it. She was having headache. She was having headache on one side of head, also one week has been down. She was having serious headache and she just wanted to know if this was something that has been reported. Patient stated after the vaccine, she was having sore arms, noticed some heart palpitations, also didn't feel any nausea, chills and pulse (pending clarification). But she did feel like she has been hit by a truck. It liked knock her out. She was out for like two days. She had recently been having headache on one side of head. When she bend down, she felt a lot of pressure on one side of head and also light. She was very sensitive to light one side of head. Patient was receiving ongoing Tylenol 500mg, 2 tablet, twice a day as treatment. Onset date of "headache on one side of head/ serious headache" and "feel a lot of pressure on one side of head" was 04Apr2021. Outcome of event "headache on one side of head/ serious headache" and "feel a lot of pressure on one side of head" was not recovered, of the other events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 636,615

Page last modified: 03 October 2021 5:28pm