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**
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Manufacturers

Total Manufacturer

Incidents per State

State Total
72,296
AK1,638
AL5,339
AR3,412
AS44
AZ13,316
CA58,147
CO11,002
CT7,824
DC1,626
DE1,670
FL36,235
FM3
GA13,429
GU82
HI2,195
IA4,332
ID2,473
IL19,261
IN22,568
KS4,284
KY6,945
LA4,714
MA13,886
MD11,901
ME2,997
MH8
MI17,865
MN11,345
MO8,919
MP30
MS2,676
MT2,147
NC15,401
ND1,273
NE2,732
NH2,859
NJ17,232
NM3,702
NV4,071
NY32,763
OH18,072
OK5,940
OR7,954
PA22,457
PR2,104
QM2
RI1,911
SC6,055
SD1,133
TN8,691
TX34,122
UT4,023
VA13,944
VI49
VT1,661
WA13,811
WI10,395
WV2,220
WY805
XB5
XL1
XV2

ID: 1360206
Sex: F
Age:
State: CA

Vax Date: 02/26/2021
Onset Date: 02/26/2021
Rec V Date: 05/29/2021
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Symptoms: Sore arm; weakness; This is a spontaneous report from a contactable consumer (patient). A 49-year-old female patient not pregnant received bnt162b2 (BNT162B2), via an unspecified route of administration, administered in Arm Left on 26Feb2021 13:00 (Lot Number: EN6203) as single dose (at age of 49-year-old) for covid-19 immunisation. Medical history was reported as none. Patient had no known allergies. There were no concomitant medications. Patient did not receive any other vaccine in four weeks. Patient did not have COVID prior vaccination and also patient was not tested for COVID post vaccination. On 26Feb2021 15:00 patient experienced sore arm and weakness. No treatment was received. Patient was recovering from the events. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1360207
Sex: F
Age:
State: TX

Vax Date: 02/26/2021
Onset Date: 02/27/2021
Rec V Date: 05/29/2021
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Symptoms: Headache; Severe Pain In Left Hand; Overall Body Aches; Low Grade Fever 101.3; NAUSEA; Fatigue; This is a spontaneous report received from a contactable consumer (patient). This 68-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection Lot Number and Expiration Date was not reported), via an unspecified route of administration in left arm on 26Feb2021 at 12:30 PM, as 2nd dose, single dose for covid-19 immunisation. Patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), Solution for injection, Batch/lot number: EL9269, Expiration date: unknown), via an unspecified route of administration in right arm, on 07Feb2021 at 1:15, at a single dose for covid-19 immunization. The patient's medical history, known allergy and concomitant medications were not reported. The patient did not receive any other medication in four weeks. She received progesterone: furazolidone, metronidazole (DIM), adk, and eszopiclone (LUNESTA) in two weeks. The patient did not have covid prior vaccination. On 27Feb2021 at 1:30, the patient experienced headache, serve pain in left hand, overall body aches, low grade fever 101.3, nausea, and fatigue. No treatment was received for the AE. The outcome of events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: PROGESTERONE; LUNESTA; DIM [FURAZOLIDONE;METRONIDAZOLE]

Current Illness:

ID: 1360208
Sex: F
Age:
State: FL

Vax Date: 02/27/2021
Onset Date: 02/28/2021
Rec V Date: 05/29/2021
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Symptoms: headache; Runny Nose; Soar Throat; This is a spontaneous report from a contactable consumer. A 68-years-old female patient received first dose of BNT162B2 ( PFIZER-BIONTECH COVID-19 VACCINE, Formulation:solution for injection, Lot Number: EN6201) via an unspecified route of administration, administered in Arm Left on 27Feb2021 at 13:00 as single dose for covid-19 immunization. The patients medical history was and concomitant medications were not reported. Patient did not received vaccine in four weeks. Patient had no covid prior to vaccination. Patient was not tested for covid post vaccination. On 28Feb2021 at 01:00 AM Patient experienced runny nose- rhinorrhea, Sore Throat and headache. The outcome of the events was unknown. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1360209
Sex: M
Age:
State:

Vax Date: 02/18/2021
Onset Date: 02/19/2021
Rec V Date: 05/29/2021
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Symptoms: Very mild headache; shortness of breath; This is a spontaneous report from a non-contactable consumer or other non hcp. A 35-years-old male patient received bnt162b2, (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EL3247), via an unspecified route of administration on 18Feb2021 as 1st dose, single for COVID-19 immunization (at the age of 35 years). The patient medical history and concomitant medications were not reported. Patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. On 19Feb2021, the patient experienced very mild headache and shortness of breath for about 1-2 hours. Patient did not receive any treatment for adverse events. The outcome of event was recovered on an unspecified date. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1360210
Sex: M
Age:
State: MI

Vax Date: 02/26/2021
Onset Date: 02/27/2021
Rec V Date: 05/29/2021
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Symptoms: Headache; Light headedness/dizziness; Body ache; Fatigue; Sore lung muscles on front and back; Tightness in chest; This is a spontaneous report from a contactable consumer. A 28-years old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EN6168), via an unspecified route of administration in left arm on 26Feb2021 at 14:00 as a single dose for COVID-19 immunization. The patient received vaccination at field house facility. The patient did not receive any other vaccine with in four weeks of COVID vaccination. The patient was not diagnosed with COVID prior vaccination. The patient did not undergo COVID test post vaccination. The patient had no known allergies. The patient's medical history and concomitant medications were not reported. On 27Feb2021 at 17:00, the patient experienced headache, dizziness, light headedness, body ache, fatigue, sore lung muscles on front and back, tightness in chest. The patient did not receive any treatment medication for the events. The outcome of the events was recovering. No follow-up attempts are possible. No further information was expected.

Other Meds:

Current Illness:

ID: 1360211
Sex: F
Age:
State: OH

Vax Date: 02/26/2021
Onset Date: 02/26/2021
Rec V Date: 05/29/2021
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Symptoms: Severe headache; extreme body aches; extreme fatigue; light headed when not lying down; feeling like I was going to vomit if not lying down; This is a spontaneous report from a contactable consumer (Patient). A 61-year-old (non-pregnant) female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: EN6202), via an unspecified route of administration, administered in arm left on 26Feb2021 09:45 as single dose for covid-19 immunisation. Medical history included high cholesterol, penicillin allergy, allergies to sulfa and covid-19. Patient previously took thiomersal and had allergy from it. Concomitant medication included rosuvastatin (other medications in two weeks). The patient did not receive any other vaccines within 4 weeks. Patient had covid prior vaccination. The patient was not tested for COVID post vaccination. On 26Feb2021, the patient experienced severe headache, extreme body aches, extreme fatigue, light headed when not lying down, feeling like I was going to vomit if not lying down. The treatment was not received for adverse event. The outcome of events was recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: ROSUVASTATIN

Current Illness:

ID: 1360212
Sex: F
Age:
State:

Vax Date: 02/22/2021
Onset Date:
Rec V Date: 05/29/2021
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Symptoms: Headache; body aches; sore arm; This is a spontaneous report from a non-contactable consumer or other non hcp (Patient herself). A 36-years-old female (Non pregnant) patient received bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Batch/Lot number: unknown), via an unspecified route of administration on 22Feb2021 at 14:00 (Age at time of vaccination 36-years-old) as unknown single, dose for covid-19 immunization. The patient medical history, concomitant medications were not reported. The patient has not covid tested before vaccination and after vaccination. No treatment received. The patient had no other vaccine in four weeks. On an unspecified date the patient experienced Headache, body aches, sore arm. The outcome of event was recovered. No follow-up attempts are Possible. Information on lot/batch cannot be obtained.

Other Meds:

Current Illness:

ID: 1360213
Sex: F
Age:
State: MT

Vax Date: 02/26/2021
Onset Date: 02/26/2021
Rec V Date: 05/29/2021
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Symptoms: Headache; dizziness; fatigue; chills; body aches; This is a spontaneous report from a contactable other hcp. A 41-year-old non-pregnant female patient received first dose bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: solution for injection, Batch/Lot Number: EN6202; Expiration date was unknown), via an unspecified route of administration, administered in Arm Left on 26Feb2021 12:00 (age at vaccination 41-year-old) as 1ST DOSE, SINGLE for covid-19 immunization. The vaccine facility was other. Medical history included asthma, allergy, depression, ADHD, long haul Covid symptoms, covid-19, known allergies: Cats and mold. Concomitant medications included lisdexamfetamine mesilate (VYVANSE); escitalopram oxalate (LEXAPRO); dienogest, ethinylestradiol (LARISSA); montelukast sodium; budesonide, formoterol fumarate (SYMBICORT). On 26Feb2021 at 19:00, the patient experienced headache, dizziness, fatigue, chills, body aches. Patient reports about the covid vaccine. Patient had no other vaccination in four weeks. Reported that patient had covid prior to vaccination and not tested post vaccination. Patient was not received any treatment. The outcome of event was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: VYVANSE; LEXAPRO; LARISSA; SINGULAIR; SYMBICORT

Current Illness:

ID: 1360214
Sex: M
Age:
State: NM

Vax Date: 12/23/2020
Onset Date:
Rec V Date: 05/29/2021
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Symptoms: headache; This is a spontaneous report from a contactable pharmacist. A 30-years-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EL1284, Expiration date not reported), intramuscular in left arm on 23Dec2020 at 13:15 (at the age of 30-year-old) as a single dose for COVID-19 immunisation. The patient was allergic to azithromycin and ibuprofen. Medical history included covid-19 prior vaccination. Since the vaccination, the patient had not been tested for COVID-19. Concomitant medications were not reported. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient experienced no reaction with 1st vaccine 1155 c/o headache on an unspecified date. The seriousness of headache was reported as non-serious. The outcome of headache was reported as recovered. No follow up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1360215
Sex: F
Age:
State: CA

Vax Date: 02/24/2021
Onset Date: 02/24/2021
Rec V Date: 05/29/2021
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Symptoms: Chills; Body ache; Sore arm; This is a spontaneous report from a contactable pharmacist (patient) who reported events after first and second dose of the vaccine. This case is for events after the second dose. A 31-year-old Female patient (not pregnant) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number: EM9810), via an unspecified route of administration, in Right arm on 24Feb2021 (at 31 years) at single dose for covid-19 immunisation . Patient had known allergy to Cantaloupe. Concomitant medications included multivitamin; ascorbic acid/herbal nos/levoglutamide/lysine/magnesium/manganese/retinol/riboflavin/selenium/tocopherol/zinc (AIRBORNE) and ibuprofen (ADVIL) for 2 days between doses. Previously on 03Feb2021 at 16:30 (at 30 years) patient receive first dose of the vaccine (lot EL9262) in Right arm for covid-19 immunisation and experienced sore arm for 2-3 days. On 24Feb2021 the patient experienced chills starting 12 hours after dose and lasting until about 28 hours after; body aches starting 16 hours after dose and lasting until about 28 hours after and sore arm for 2-3 days. No treatment given. The outcome of the events was recovered in Feb2021. No follow up attempts are possible; information on Lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021219538 same patient/vaccine, different dose/event.

Other Meds: AIRBORNE; ADVIL [IBUPROFEN]

Current Illness:

ID: 1360216
Sex: F
Age:
State: NC

Vax Date: 02/24/2021
Onset Date:
Rec V Date: 05/29/2021
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Symptoms: a little tired hazy headache; intense burning in my chest; shaking jittery/ frightend; This a spontaneous report from a contactable consumer (patient). An elderly non pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTEC COVID-19 VACCINE, Solution for injection, Lot Number: EN62020 and expiry date was not provided), via an unspecified route of administration, in the left arm on 24Feb2021 at 16:00 as a single dose for COVID-19 immunisation. Medical history included skin cancer, kidney stones, HBP treated, arthritis and had skin cancer surgery removed 5 weeks ago center upper chest which involved injected anesthesia. Patient had allergies (unspecified). Concomitant medication included levothyroxine, liothyronine (NP THYROID); Olmesartan; citalopram and vitamins nos (MULTI-VITAMINS). She did not receive other vaccine in four weeks of vaccination. She did receive other medications in two weeks of vaccinations. She was not diagnosed with COVID, prior vaccination. She had not been tested for COVID, post vaccination. On an unknown date, patient experienced no problem for the first hours then a little tired hazy headache. Took paracetamol (TYLENOL) and went to bed early. Patient awoke in night by an intense burning in chest and was shaking jittery/ frightend. Patient had no serious fever and could breathe ok. She took 2 paracetamol (TYLENOL) and tried to go back to sleep. She felt better in the morning but still lingering burning sensation almost like underneath skin and was scalded or sunburn. She went to physician office and took diphenhydramine hydrochloride, paracetamol (TYLENOL PM) 2nd night. Better by 4th day but still did not feel normal. It was unknown if any treatment received. The outcome of events was recovered with lasting effects. No follow up attempts are possible. No further information is expected.

Other Meds: NP THYROID; OLMESARTAN; CITALOPRAM; MULTIVITAMINUM

Current Illness:

ID: 1360217
Sex: F
Age:
State: OK

Vax Date: 02/27/2021
Onset Date: 02/27/2021
Rec V Date: 05/29/2021
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Symptoms: Headache; muscle soreness; cramping/diarrhea; fatigue; sight injection pain; cramping; This is a spontaneous report from a contactable consumer (the patient). A 54-Year-old non-pregnant female patient received first dose bnt162b2 (Pfizer's COVID-19 vaccine, Solution for injection (Batch no: not reported, expiration: not reported), via an unspecified route of administration on Right arm on 27Feb2021 at 11:30 AM at single dose for covid-19 immunization. The patient medical history include neuropathy. The concomitant medications include Gabapentin, Eliquis, CBD/THC, Bariatric Vitamins. Patient was allergic to PCN, Demerol, Percocet, Iodine, latex, Tetanus. Patient did not have covid prior vaccination. Patient had not tested covid post vaccination. Patient did not had other vaccine in four weeks. On 27Feb2021 at 04:00 PM, the patient experienced headache, muscle soreness, cramping/diarrhea, fatigue and sight injection pain. The outcome of the events was recovering. No follow-up attempts are possible. Information on the batch/lot number cannot be requested.

Other Meds: ELIQUIS; GABAPENTIN

Current Illness:

ID: 1360218
Sex: F
Age:
State: KY

Vax Date: 02/24/2021
Onset Date: 02/28/2021
Rec V Date: 05/29/2021
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Symptoms: headache; cold chills; Fever; Had aches; This is a spontaneous report from a contactable consumer(patient). A 72-year-old female received of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number; EN6198 and Expiration date was not reported), via an unknown route of administration in right arm on 24Feb2021 at 16:00(at the age of 72-year-old), as 1st dose, single for COVID-19 immunization. The patient medical history including any illness at time of vaccination were none. The vaccine was not administered at military facility. History of all previous immunization with the Pfizer vaccine considered as suspect was none. Additional vaccines administered on same date of the Pfizer suspect was not provided. Prior vaccinations within 4 weeks were none. The concomitant medications were not reported. Patient received the first dose of the Pfizer Covid 19 vaccine last wednesday on 24Feb2021. She felt fine after vaccination. On 28Feb2021, she started having fever (of 99.8, which her normal is 97.4), fever broke at 11pm last night and no other fever. The fever broke, she discovered she had a fever and then about 7 hours later it broke, she had taken some Tylenol. She had cold chills and had a real bad headache that lasted for about 24 hours and today she does not have a fever, her fever broke. She said it started, about all day long she had a headache and they have had some crazy weather so she thought it may have been the barometric pressure and then she started having the cold chills in afternoon and the temperature, usually she did not run a fever, so she was a little concerned, she said she hopes she didn't have COVID but she still had her taste and smell and she checked her temperature and she has no fever today. The chills are somewhat resolved but she was still chilly even with the heat on and extra clothes she was cold. She said the chills are ongoing but improved. She no longer has the headache today. She confirmed fever chills and headaches was everything she experienced following the vaccine. She doesn't feel really good either and she was wondering if it is normal that many days after the vaccination to have side effects. The events did not require visit to emergency room and physician office. She complained a product complaint.The outcome of the event had aches was unknown and for the event chills was recovering, whereas headache and fever was recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1360219
Sex: F
Age:
State: NJ

Vax Date: 02/22/2021
Onset Date: 02/22/2021
Rec V Date: 05/29/2021
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Symptoms: Generally feeling horribly; Four days later terrible body aches; chills; vomiting and a headache that lasted for 36 hours; Headache; Seven days later, still lethargic and fatigued; fatigue; This is a spontaneous report received from a contactable consumer (patient). A 58-year-old (non-pregnant) female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number: EL9266) via an unspecified route of administration, administered in left arm on 22Feb2021 at 10:30 AM as 1st dose single for covid-19 immunisation. The patient medical history included breast cancer on an unknown date in 2015. The patient had known allergy with penicillin. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient's concomitant medications included tamoxifen, ergocalciferol (VIT D), calcium,, acetylsalicylic acid (BABY ASPIRIN) and ascorbic acid, chromium, copper, folic acid, inositol, magnesium, manganese, nicotinamide, pantothenic acid, potassium, pyridoxine hydrochloride, retinol, riboflavin, selenium, vitamin b1 nos, vitamin b12 nos (MULTI VIT) in two weeks of vaccination. On 22Feb2021 (the night of 1st shot vaccination), the patient experienced headache. On 26Feb2021, four days later, the patient experienced terrible body aches, chills, vomiting and a headache that lasted for 36 hours. The patient was generally feeling horribly and seven days later still lethargic and fatigued was continued. The patient did not receive treatment for the events. The patient had not covid tested post vaccination and patient had no covid prior vaccination. The outcome of the events was recovered on an unknown date in 2021. It was reported that patient was recovered with lasting effects. No follow-up attempts are possible. No further information is expected.

Other Meds: TAMOXIFEN; VIT D; CALCIUM; BABY ASPIRIN; MULTI VIT

Current Illness:

ID: 1360220
Sex: F
Age:
State: NV

Vax Date: 02/27/2021
Onset Date: 02/28/2021
Rec V Date: 05/29/2021
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Symptoms: Severe Headache; major fatigue; body ache; stomach pain; This is a spontaneous report from a contactable consumer (patient) via COVID-19 Adverse Event Self Reporting. A 70-years-old non-pregnant female received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 2 via an unspecified route of administration in arm right on 27Feb2021 at 12:00 (Batch/Lot Number: EN6205) (at the age of 70-years-old) as a single dose for COVID-19 immunization. Medical history included thyroid and high cholesterol. Patient was allergic to CAT scan dye. Patient previously took bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration in arm left on 06Feb2021 at 12:00 (Batch/Lot Number: EL9269) (at the age of 70-years-old) as a single dose for COVID-19 immunization. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19 and was not tested for COVID post vaccination. The patient took other medications (unspecified) within two weeks near to vaccination date. On 28Feb2021 at 02:00 AM, the patient experienced severe headache, major fatigue, body aches and stomach pain. No treatment was provided for the events. The outcome of the events was unknown. Follow-up (14May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1360221
Sex: F
Age:
State: OH

Vax Date:
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Rec V Date: 05/29/2021
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Symptoms: headache; chills; ache; This is a spontaneous report from a contactable consumer (patient). A 71 years-old female patient (not pregnant at the time of vaccination) received second dose of BNT162B2 (Solution for Injection, lot number: EL9269, Expiration date: unknown), via an unspecified route of administration on 26Feb2021, at 06:00 PM (at 71-years-age) as 2nd dose, single dose for covid-19 immunisation and received first dose of BNT162B2 (Solution for Injection, lot number, Expiration date: unknown), via an unspecified route of administration on an unspecified date as 1st dose, single dose for covid-19 immunisation. Other vaccination date reported as Feb2021. The patient medical history and concomitant medications were not reported. Patient did not receive any other vaccines within 4 weeks previous to the COVID vaccine. On an unspecified date, the patient experienced headache, chills and aches after 24 hours of vaccination. No Treatment received for the events. The outcome of the events was recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1360222
Sex: F
Age:
State: NY

Vax Date: 03/01/2021
Onset Date: 03/01/2021
Rec V Date: 05/29/2021
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Symptoms: sore arm; Headache and dizziness as if I had hit my head or got anesthesia and was about to go out; Headache and dizziness as if I had hit my head or got anesthesia and was about to go out; feeling of heaviness/heaviness in my head; This is a spontaneous report from a contactable consumer (patient). A 51-year-old non pregnant female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/lot number: Unknown) via an unspecified route of administration, administered in left arm on 01Mar2021 at 13:00 (at the age of 51-year-old) at a single dose for covid-19 immunisation in workplace clinic. Medical history included hypothyroidism and autoimmune disorders. Patient was not allergic to medications, food, or other products. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Concomitant medications included levothyroxine sodium (SYNTHROID) at a dose of 112 mg daily, calcium and vitamin supplement. Prior to vaccination the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 01Mar2021 at 13:15, minutes after vaccination when the patient was sitting in the waiting/observation area the patient experienced headache and dizziness as if the patient had hit her head or got aneathesia and was about to go out and had feeling of heaviness/heaviness in her head. Patient stayed a bit longer when she thought she could leave 15-20 minutes after the feeling started to subside and but when she tried to walk and go upstairs dizziness and feeling of heaviness was persisted, got better with lots of water. Overall, about 2 hours later around 3- 3.30 pm she was feeling better and went home. That evening around 8 pm, she felt ok without the dizziness or heaviness in her head. She only had a sore arm and was ok the next day. No treatment was received to the patient for the events. The outcome of event sore arm was recovering, rest of the events was recovered. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: SYNTHROID; CALCIUM; VITAMINS NOS

Current Illness:

ID: 1360223
Sex: F
Age:
State: MO

Vax Date: 02/16/2021
Onset Date: 02/17/2021
Rec V Date: 05/29/2021
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Symptoms: Headache with little bump on the neck area (lymph node swollen); Headache with little bump on the neck area (lymph node swollen); Headache with little bump on the neck area/The bump was sore; This is a spontaneous report from a contactable consumer or other non healthcare. A 27-years-old non-pregnant female patient received first dose BNT162B2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: EN5318), via an unspecified route of administration, administered in arm right on 16Feb2021 at 09:45 as 1st dose, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Patient had no known allergies. The patient did not receive any other vaccine in four weeks. Patient did not receive other medications in two weeks. Patient was not covid prior vaccination. On 17Feb2021 at 08:00 the patient experienced headache with little bump on the neck and lymph node swollen. The patient was vaccinated at the workplace clinic. It was reported that the patient had headache with little bump on the neck area (lymph node swollen) on the next day. The bump was sore. Headache and the little bump was gone by the third day of vaccination. Patient was not covid tested post vaccination. Patient did not received treatment for AE. Outcome of the event neck pain was unknown and the outcome of the other two events were recovered on an unspecified date. No follow-up attempts are possible. No further information is expected.

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Current Illness:

ID: 1360224
Sex: F
Age:
State: IN

Vax Date: 02/25/2021
Onset Date:
Rec V Date: 05/29/2021
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Symptoms: headache; neck pain; This is a spontaneous report from a contactable consumer, on behalf of his wife via Pfizer-sponsored program. A 73-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) via an unspecified route of administration on 25Feb2021 as single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, patient slept wrong and experienced neck pain. Patient also had headache. Reporter was asking ibuprofen could be taken for the headache due to the wrong sleeping position. 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: 1360225
Sex: F
Age:
State: MA

Vax Date: 02/25/2021
Onset Date: 02/26/2021
Rec V Date: 05/29/2021
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Symptoms: Dull on and off headache 24 hours post second dose that lasted for 24 hours; Diarrhea 34 hours post second dose that lasted approximately 6 hours.; This is a spontaneous report from a contactable consumer (patient). A 59-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EL3247 and expiry date was not reported), via an unspecified route of administration, administered in arm right on 25Feb2021 at 02:15 as a single dose for covid-19 immunisation. The patient had no medical history. Concomitant medications were not reported. Patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number and expiry date was not reported), via an unspecified route of administration on unspecified date as single dose for covid-19 immunisation. Patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. No medications in 2 weeks. On 26Feb2021 (reported as at 16:00), 24 hours post second dose patient experienced dull on and off headache post second dose that lasted for 24 hours and diarrhoea 34 hours post second dose that lasted approximately 6 hours. No treatments were received for the events. The outcome of the events was recovered on unspecified date. No follow-up attempts are possible. No further information is expected.

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Current Illness:

ID: 1360226
Sex: F
Age:
State:

Vax Date: 02/16/2021
Onset Date: 02/20/2021
Rec V Date: 05/29/2021
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Symptoms: pain/fatigue in neck and shoulders; sharp pains in the head, like a burning sensation; pain/fatigue in neck and shoulders; pain/fatigue in neck and shoulders; sharp pains in the head, like a burning sensation; This is a spontaneous report from a contactable consumer (patient). A 47-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 16Feb2021 as single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. On 20Feb2021, the patient experienced, the patient received first dose Pfizer on 16feb2021 4 days after the shot she developed sharp pains in the head, like a burning sensation, with pain/fatigue in neck and shoulders. Pain was still ongoing. The outcome of events headache, burning sensation, fatigue was unknown whereas pain was not recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

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Current Illness:

ID: 1360227
Sex: M
Age:
State: CA

Vax Date: 02/19/2021
Onset Date: 02/20/2021
Rec V Date: 05/29/2021
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Symptoms: headache; Sore arm; muscle aches; weakness; congestion; This is a spontaneous report from a contactable consumer. A 67-years-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection), via an unspecified route of administration, administered in Arm Left on 19Feb2021 at 11:45 (Batch/Lot Number: EN6200) as 2nd dose, single for covid-19 immunization. Medical history included High blood pressure, high blood cholesterol and ascending aortic aneurysm. The patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection), via an unspecified route of administration, administered in Arm Left on 27Jan2021 at 4:30 (Batch/Lot Number: EL982) as 1st dose, single for covid-19 immunization.Concomitant medications within 2 weeks included rosuvastatin calcium (CRESTOR), ezetimibe (ZETIA), omeprazole (PRILOSEC [OMEPRAZOLE]) and low dose acetylsalicylic acid (ASPIRIN ). Patient did not take other vaccines in four weeks. Patient did not had Allergies. The patient had Covid prior vaccination.The patient tested Covid post vaccination on 19May2020 which was negative. On 20Feb2021 at 09:00 the patient experienced headache, sore arm, muscle aches, weakness, congestion for about 36hours. No treatment was administered for the events. The patient was recovered from the events in 2021. No follow up attempts are possible. No further information is expected.

Other Meds: CRESTOR; ZETIA; PRILOSEC [OMEPRAZOLE]; ASPIRIN

Current Illness:

ID: 1360228
Sex: F
Age:
State: CA

Vax Date: 02/26/2021
Onset Date: 02/27/2021
Rec V Date: 05/29/2021
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Symptoms: headache; low energy; body aches; This is a spontaneous report from a contactable consumer (patient) reported for herself. A 77-years-old female patient (patient was not pregnant at the time of vaccination) received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EN6203, Expiration Date: unknown) via an unspecified route of administration, administered in left arm on 26Feb2021 at 11:00 am (age at vaccination was 77 years) as 2ND DOSE, SINGLE DOSE for COVID-19 immunization. The patient's medical history included atrial fibrillation and high blood pressure. The patient did not have any allergies. Concomitant medication patient received within 2 weeks of vaccination included rivaroxaban (XARELTO), nebivolol hydrochloride (BYSTOLIC), atorvastatin and amlodipine besilate, olmesartan medoxomil (OLMESARTAN E AMLODIPINA EG). The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot Number: EI9265, Expiration Date: unknown) via an unspecified route of administration, administered in left arm on 05Feb2021 at 11:00 am (age at vaccination was 77 years) as 1ST DOSE, SINGLE DOSE for COVID-19 immunization. On 27Feb2021 at 19:00 pm, the patient experienced headache, low energy and body aches. Today on 01Mar2021, 3 days after second dose patient was still experiencing headache, low energy, and body aches. 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 has not been tested for COVID-19. The patient underwent lab tests and procedures which included blood pressure measurement: high on an unknown date. The patient received treatment with Tylenol Extra Strength. The outcome of events was not resolved. No follow-up attempts are needed. No further information is expected.

Other Meds: XARELTO; BYSTOLIC; ATORVASTATIN; OLMESARTAN E AMLODIPINA EG

Current Illness:

ID: 1360229
Sex: M
Age:
State: UT

Vax Date: 02/25/2021
Onset Date: 02/26/2021
Rec V Date: 05/29/2021
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Symptoms: headache; dry hacking cough; running nose; repeated sneezing; Rapid heartbeat; body ache's; This is a spontaneous report from a contactable consumer (patient, self-reported). A 63-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, in Arm Left, on 25Feb2021 at 07:15 AM, as a single dose for COVID-19 immunization. The patient did not receive any other vaccine in four weeks. The patient's medical history included HIV+, chronic bronchitis, asthma, and arrhythmia. It was unknown if the patient had known allergies. The patient received unspecified medications in two weeks. The patient was not diagnosed with COVID prior vaccination. The patient was not tested for COVID post vaccination. The patient reported that on 26Feb2021 at 02:30 PM, approx 20 hrs later, she started with a headache and a dry hacking cough, developed a running nose then repeated sneezing. She also had rapid heartbeat and body ache's at about 24 hrs. Symptoms continued through Saturday and Sunday. She felt better today (Monday 01Mar2021) but body aches were returning around 3:30 pm still had a headache and it had never gone away. The patient did not receive any treatment for the events. Outcome of the events was recovering. No follow-up attempts are possible. Information about lot/batch number cannot be obtained. No further information is expected.

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Current Illness:

ID: 1360230
Sex: F
Age:
State: CA

Vax Date: 02/22/2021
Onset Date: 02/23/2021
Rec V Date: 05/29/2021
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Symptoms: Headache; muscle ache; nausea; This is a spontaneous report from a contactable consumer or other non-hcp (Patient). A 71-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation solution for injection; Lot Number: EL9266) via an unspecified route of administration in Left Arm on 22Feb2021 02:30 PM as 1st dose single for COVID-19 immunization. Medical history included diabetes mellitus from an unknown date and unknown if ongoing. Concomitant medication included dulaglutide, metformin, atorvastatin and estrogens conjugated taken for an unspecified indication, start and stop date were not reported. The patient does not have allergies. It was reported that the patient has not taken any other vaccine in four weeks. On 23Feb2021 07:00 AM; the patient experienced headache, muscle ache and nausea. The seriousness of the events was reported as non-serious. The clinical outcome of the events was recovered. No follow-up attempts are possible. No further information expected.

Other Meds: TRULICITY; METFORMIN; ATORVASTATIN; ESTROGENS CONJUGATED

Current Illness:

ID: 1360231
Sex: F
Age:
State:

Vax Date: 02/08/2021
Onset Date: 02/09/2021
Rec V Date: 05/29/2021
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Symptoms: I had general joint pain starting the day after the vaccine. After two days it all went away except my knees. I have never had any issues with my joints or knees before this.; By the end of the day it hurts a lot to walk up stairs.; This is a spontaneous report from a contactable other health care professional. A 40-years-old non pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EM9809), dose 1 via an unspecified route of administration, administered in left arm on 08Feb2021 at 10:00 AM as 1ST DOSE, SINGLE for covid-19 immunisation. Medical history included drug hypersensitivity, iodine allergy, autoimmune thyroiditis. Concomitant medication included levothyroxine sodium (SYNTHROID). No COVID prior vaccination. COVID tested post vaccination was no. On 09Feb2021 at 09:00 AM, the patient experienced general joint pain starting the day after the vaccine. After two days it all went away except my knees. I have never had any issues with my joints or knees before this. It started suddenly after the vaccine. Two weeks after the vaccine my knees are still sore. By the end of the day it hurts a lot to walk up stairs. Throughout the day they feel mildly sore and will sometimes click as I bend them. Treatment was not received for the events. The outcome of events were not recovered. Follow-up attempts completed. No further information expected.

Other Meds: SYNTHROID

Current Illness:

ID: 1360232
Sex: U
Age:
State:

Vax Date: 02/20/2021
Onset Date: 02/01/2021
Rec V Date: 05/29/2021
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Symptoms: Pain at the back; This is a spontaneous report from a contactable consumer or other non hcp. A patient of unspecified age and gender received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration on 20Feb2021(Batch/Lot number was not reported) as 1ST DOSE, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. In Feb 2021, The patient experienced pain at the back. The patient reported that patient had vaccine, last Saturday and everything seems to be fine except last night. Last night, patient experienced pain at the back, at lower back below the waistline. The patient enquired was that common. Patient had the first dose last saturday. The outcome of event was unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1360233
Sex: F
Age:
State:

Vax Date: 02/19/2021
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Rec V Date: 05/29/2021
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Symptoms: Cold fingers and toes; discoloration; numbness; This is a spontaneous report from a contactable other HCP(Patient). This 30-year-old non-pregnant female received her second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number: Em9810), via an unspecified route of administration in right arm on 19Feb2021 at 07:00 PM (at the age of 30-year-old) as a single dose for COVID-19 Immunization, at hospital. Patient's medical history included Covid-19. Concomitant medications included multivitamins [vitamins nos] and melatonin;theanine (medications in 2 weeks). The patient previously took first dose of BNT62b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Lot number El9264) for on 29Jan2021 at 07:00 PM via an unspecified route of administration in right arm at single dose for COVID-19 Immunization. Prior to the vaccination the patient was diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Patient did not receive other vaccines in four weeks of vaccination. Adverse event resulted in Doctor or other healthcare professional office/clinic visit. Patient experienced cold fingers and toes; podiatrist said it appeared to have smaller capillaries in his toes led to discoloration and numbness. No treatment was given for the event. The outcome of events was unknown. Follow-up (11May2021): Follow-up attempts completed. No further information expected.

Other Meds: MELATONIN;THEANINE

Current Illness:

ID: 1360234
Sex: U
Age:
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Symptoms: I started to getting metallic taste in my mouth; This is a spontaneous report from a contactable consumer (Patient). A patient of unspecified age and gender received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number: Unknown) as 1ST DOSE, SINGLE for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. On an unspecified date around 5 days after the vaccination, the patient had metallic taste in mouth. It was reported that the patient informed physician about this, blood work was performed and no further details were provided. Outcome of event was unknown. Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1360235
Sex: F
Age:
State:

Vax Date: 02/22/2021
Onset Date: 02/01/2021
Rec V Date: 05/29/2021
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Symptoms: Sore arm; mild chills; fatigue; mild headache/medium headache; This is a spontaneous report from a non-contactable consumer. An adult (18-64) female patient started to received first dose of bnt162b2 (BNT162B2), via an unspecified route of administration on 22Feb2021 (Batch/Lot Number: EL3247) as single dose for covid-19 immunisation .The patient medical history and concomitant medications were not reported. On 22Feb2021 within 12 hours of injection the patient experienced sore arm, mild chills, fatigue and mild headache between 24-36 hours; medium headache between 36-48 hours (both resolved with oral Advil, 3x 200mg total). The outcome of the events was recovered on an unspecified date. No follow-up attempts are possible. No further information is expected.

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Current Illness:

ID: 1360236
Sex: F
Age:
State: CA

Vax Date: 02/11/2021
Onset Date: 02/25/2021
Rec V Date: 05/29/2021
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Symptoms: headache; severe rashes in my forehead; bumps puffy face; swollen lymphnodes on the right side; sensitive to touch itching, and burning; sensitive to touch itching, and burning; This is a spontaneous report from a contactable other hcp (patient). A 60-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Lot Number: EN6201), dose 1 intramuscular, administered in Arm Right on 11Feb2021 at 10:30 (at the age of 60 years old) as 1st dose, single for COVID-19 immunization. Medical history included hypothyroidism, mild hypertension, acid reflux from an unknown date and unknown if ongoing. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient was allergic to aspirin, NSAID, shellfish and some other fish. Concomitant medications included atorvastatin calcium (ATORVASTATIN CALCIUM); metoprolol tartrate (METOPROLOL TARTRATE); omeprazole (OMEPRAZOLE); levothyroxine sodium (LEVOTHYROXINE SODIUM) taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines within four weeks. On 25Feb2021, 15 days after the first dose she got a headache, severe rashes in my forehead, bumps puffy face, swollen lymph nodes on the right side only sensitive to touch itching, and burning. The symptoms are beginning to subside now but was scheduled to get her 2nd dose on March 4th. She would like some guidance. The patient was treated with antibiotics. The patient visited physician office due to events. The outcome of the events was recovering. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: ATORVASTATIN CALCIUM; METOPROLOL TARTRATE; OMEPRAZOLE; LEVOTHYROXINE SODIUM

Current Illness:

ID: 1360237
Sex: F
Age:
State:

Vax Date: 02/23/2021
Onset Date: 02/23/2021
Rec V Date: 05/29/2021
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Symptoms: night sweat; Fatigue; Sore arm; Nausea; Chills; This is a spontaneous report from a contactable consumer (reporting for herself). A 30-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE,Batch/Lot Number: EL3247), dose 2 via an unspecified route of administration, administered in Arm Left on 23Feb2021 11:15 (at the age of 30-year-old) as 2ND DOSE, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Historical vaccine included BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# EL3247), dose 1, via an unspecified route of administration single dose arm left on 02Feb2021 23:15 for covid-19 immunisation. The patient did not receive any other vaccines within four 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 for COVID-19. On 23Feb2021 at 23:00, the patient experienced night sweat, fatigue, sore arm, nausea and chills. No treatment received. The outcome of the events was recovering. Follow-up (14May2021): Follow-up attempts completed. No further information expected.

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Current Illness:

ID: 1360238
Sex: F
Age:
State:

Vax Date: 02/06/2021
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Rec V Date: 05/29/2021
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Symptoms: aching; Allergies; This is a spontaneous report from a contactable consumer or other non HCP. A 73-year-old female patient received bnt162b2 (PFIZER BIONTECH COVID-19 mRNA Vaccine, Solution for injection, Lot Number: Unknown), dose 1 via an unspecified route of administration on 06Feb2021 as single dose for covid-19 immunization. Medical history included arthritis. The patient's concomitant medications were not reported. The patient experienced aching and allergies on an unspecified date after first dose. The patient was pretty good health other than arthritis. Every once and a while she get inflammation from the arthritis. She take ibuprofen for the inflammation. Patient has first shot on 06Feb2021 and second dose was scheduled on Saturday 27Feb2021. They have had some allergies and have orange blossoms in the back yard. It seems as though one day the patient feel great and the next day she wont. Is it safe to have the second vaccine. Her husband is 77 and he got the vaccine when I did and have noticed more aching and allergies since getting the vaccine. The patient did not receive any treatment for events. The clinical outcome of the events were unknown. Information on the lot/batch number has been requested. Follow-up attempts are completed. No further information is expected.

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Current Illness:

ID: 1360239
Sex: F
Age:
State: MA

Vax Date: 02/28/2021
Onset Date: 03/01/2021
Rec V Date: 05/29/2021
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Symptoms: This is a spontaneous report from a contactable consumer (patient herself). A 70-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; formulation solution for injection; Lot number: EN6203), via an unspecified route of administration, on 28Feb2021 17:15 (at the age of 70-year-old) in Arm Right as single dose for COVID-19 immunization. The patient medical history included sleep apnoea, COVID-19 (prior to vaccination); and patient was using continuous positive airway pressure. The patient's concomitant medications included apixaban (ELIQUIS) and metoprolol succinate (METOPROLOL SUCCINATE). On 01Mar2021 17:15, the patient experienced headache, fever (over 100F), chills, tiredness, and pain in arm. On 01Mar2021, the patient underwent laboratory test included body temperature which showed 100 Fahrenheit. The patient received treatment with Tylenol. The outcome of the reported events was resolving at the time of this report. No follow-up attempts are needed. No further information is expected.

Other Meds: ELIQUIS; METOPROLOL SUCCINATE

Current Illness:

ID: 1360240
Sex: F
Age:
State: MA

Vax Date: 02/15/2021
Onset Date: 02/28/2021
Rec V Date: 05/29/2021
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Symptoms: hives go from face to chest both sides of body; This is a spontaneous report from a contactable consumer (patient). A 76-year-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot Number: EL9261 and Expiration date was not reported), via an unspecified route of administration, administered in Arm Left on 15Feb2021 12:00 AM, as single dose for COVID-19 immunization. Medical history included sjogren's syndrome, Afib regulated and PMR. No known allergies were reported. The patient did not take other medications in two weeks. The patient did not receive other vaccine in four weeks. The patient did not had covid prior vaccination and was not tested for covid post vaccination. On 28Feb2021, 12:00 AM, the patient experienced hives which went from face to chest both sides of body. It was reported that, sunday (28Feb2021) hives go from face to chest both sides of body, never had hives before. No change in medications, food, or product use. The patient received treatment with benadryl. The outcome of the event was reported as not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1360241
Sex: F
Age:
State: ND

Vax Date: 02/24/2021
Onset Date: 02/24/2021
Rec V Date: 05/29/2021
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Symptoms: headache; muscle pain; chills; Joint pain; injection site redness swelling & pain; injection site redness swelling & pain; injection site redness swelling & pain; This is a spontaneous report from a contactable consumer or other non-HCP (patient). This 82-yerar-old non-pregnant female received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; lot number: EN6198; expiration date: unknown), via an unspecified route of administration in right arm on 24Feb2021 09:00am, as a unknown single dose for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient's medical history included hypertension, arthritis and patient had known allergy's adverse reaction to compazine. The patient's concomitant medications were metoprolol, spironolactone, HCTZ, Azelastine nasal. On 24Feb2021, the patient experienced headache, muscle pain, chills, joint pain, injection site redness, swelling & Pain. No treatment was received in response to the adverse events. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, patient was not tested for COVID-19. The outcome of events was recovered on an unspecified date of 2021. No follow-up attempts are possible. No further information is expected.

Other Meds: AZELASTINE; HCTZ; METOPROLOL; SPIRONOLACTONE

Current Illness:

ID: 1360242
Sex: F
Age:
State: FL

Vax Date: 02/26/2021
Onset Date: 02/26/2021
Rec V Date: 05/29/2021
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Symptoms: When she woke she felt like she did when she had Covid/felt like she had Covid; Chills; headache; temperature of 99.6-100.1F/Fever; I still felt a little tired; my arm was killing me; felt weird; felt weird like she was unsteady on her feet; This is a spontaneous report from a contactable consumer (patient). An 80-year-old female patient (Weight: 53.52 kg, Height: 157 cm) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration, administered in Arm Left on 26Feb2021 08:30 as 1ST DOSE, SINGLE for covid-19 immunisation. She is unable to clearly identify the Lot due to illegible handwriting on the vaccine card. She thinks it is EN6200 or EN06200. Vaccination Facility Type: Clinic sponsored by (Name). Vaccine not administered at Military Facility. Medical history included covid-19 from 2020. She was also told that she might not need to get the second dose because of having antibodies. When she had Covid it was mild. She did not have the traditional symptoms. It affected her gastrointestinal system more. It was weird. Prior Vaccinations (within 4 weeks) was None. There were no concomitant medications. On 26Feb2021, after she got the vaccine, her arm was killing her. It was awful. She took Tylenol for it. Around 3-4pm she was feeling a little bit weird/"felt a little funny" like she was unsteady on her feet. She was not dizzy. She woke up the next day, 27Feb2021, felt "rotten", "almost like I felt when I had covid/ felt like she had Covid. Same symptoms, milder form": slight headache for 3 hours, chills lasted a couple of hours, temperature of 99.6-100.1F for 3 hours. She was awful in the morning and better as the day went on. It remined her of when she had Covid. After symptoms went away, she still felt a little tired. Didn't feel as good as she did before the day she took the vaccine. Caller said the vaccination Nurse told her that she might have more reaction because she may still have antibodies. Caller asking did she need to get 2nd dose? Should she expect reactions from the second dose? She still plans on taking it. The outcome of arm was killing her was recovering. Her arm is better but if she lays on her arm she can still feel it. The outcome of felt a little tired was unknown. The patient was recovered from other events on 27Feb2021. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1360243
Sex: F
Age:
State: NC

Vax Date: 03/01/2021
Onset Date: 03/01/2021
Rec V Date: 05/29/2021
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Symptoms: Headache; vivid/anxious dreams; muscle pain in both thighs; injection site pain; vivid/anxious dreams; This is a spontaneous report from a contactable consumer (patient). A 34-year-old female patient (non-pregnant) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, Lot Number: EN6202) via an unspecified route of administration at Left arm on 01Mar2021 17:30 (at the age of 34-year-old) as 1st dose, single for COVID-19 immunisation. Medical history included Insulin resistance, endometriosis and patient previously took Ciprol and experienced Known allergies. Concomitant medication(s) included Colecalciferol VITAMIN D taken 50000 IU 1x week (other medications in two weeks). The patient did not receive any other vaccine in four weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient had not been tested for COVID-19. On 01Mar2021, patient experienced, vivid/anxious dreams, muscle pain in both thighs, injection site pain. There was no treatment for the events. Treatment recommended for AE to take Claritin and antihistamine eye. The outcome of the events was not recovered. No follow-up attempts are possible. No further information is expected.

Other Meds: VITAMIN D [COLECALCIFEROL]

Current Illness:

ID: 1360244
Sex: F
Age:
State: NJ

Vax Date: 02/24/2021
Onset Date: 02/25/2021
Rec V Date: 05/29/2021
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Symptoms: Huge Headache; Goosebumps; Dizziness; Fatigue; Soreness in arm; This is a spontaneous report from a contactable consumer. A 75-years-old non-pregnant female patient received second dose of BNT162B2 (Formulation: Solution for injection; Batch/Lot Number: EN6202), dose 2 via an unspecified route of administration, administered in arm left on 24Feb2021 as 2nd dose, single for covid-19 immunisation. Medical history included allergies with Penicillin, zinc, latex, mango. Triple negative breast cancer from 2014 to an unknown date and back pain. Concomitant medications included other medications in two weeks Levothyroxine, Vit D, Calcium. Not covid-19 prior vaccination and not covid-19 tested post vaccination. The patient received BNT162B2 (Formulation: Solution for injection; Batch/Lot Number: EL9262) dose 1 via an unspecified route of administration, administered in arm left for covid-19 immunisation on 03Feb2021. On 25Feb2021 patient experienced huge headache, goosebumps, dizziness, fatigue, soreness in arm. Patient took Advil and rested all day as treatment. No other vaccine in four weeks. The outcome of the events was recovered on an unspecified date 2021. No follow-up attempts are possible. No further information is expected.

Other Meds: LEVOTHYROXINE; CALCIUM; VITAMIN D [COLECALCIFEROL]

Current Illness:

ID: 1360245
Sex: F
Age:
State: GA

Vax Date: 02/25/2021
Onset Date: 03/02/2021
Rec V Date: 05/29/2021
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Symptoms: severe headache; Nausea; tired; This is a spontaneous report received from a contactable consumer (reporting on herself). A 72-years-old Non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection Lot Number and Expiration Date was not reported), via an unspecified route of administration in Arm Left on 25Feb2021 13:00, as 2nd dose, single dose for covid-19 immunisation. Patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection Lot Number and Expiration Date was not reported), via an unspecified route of administration in Arm Left on 04Feb2021 12:00, as 1st dose, single dose for covid-19 immunisation. Medical history included known allergies: Sulfa, Macrodantin, morphine. The patient received unspecified medication in two weeks. Prior to vaccination, the patient was not diagnosed with COVID-19 and did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Since the vaccination, the patient has not been tested for COVID-19. On 02Mar2021, day 5 woke with severe headache and nausea very tired. Patient did not received any treatment for adverse events. The outcome of the events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1360246
Sex: F
Age:
State: MD

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 05/29/2021
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Symptoms: headache; Fatigue; Chills; This is a spontaneous report from contactable pharmacist (patient). A 59-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: EN6201), via an unspecified route of administration in left arm on 25Feb2021 at 13:45 as single dose for covid-19 immunisation. Historical vaccine included first dose of BNT162B2 on 06Feb2021 at 11:45 AM for covid-19 immunisation. Medical history included Rheumatoid arthritis, HTN, hypothyroidism and Shellfish allergy. 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. Concomitant medication included Amlodipine/Valsartan 10/160, Synthroid 150mcg. On 25Feb2021 at 04:45 PM, about 3 hours post second dose developed a headache and fatigue. The following day fatigue persisted and was accompanied by chills that lasted for two days. On the third day post dose, symptoms resolved and felt normal. The patient did not received treatment due to the events. The outcome of all the events were recovered on an unspecified date in 2021. No follow-up attempts are possible. No further information is expected.

Other Meds: AMLODIPINE; VALSARTAN; SYNTHROID

Current Illness:

ID: 1360247
Sex: M
Age:
State:

Vax Date: 02/23/2021
Onset Date:
Rec V Date: 05/29/2021
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Symptoms: headache; soreness in my arm; My lymph nodes are tender; This is a spontaneous report. A contactable (age 54; Unit: Unknown) male consumer reported that: A 54-years-old male patient received bnt162b2, (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number, expiration date: not reported), via an unspecified route of administration on 23Feb2021 as 1st dose, single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient had first dose last Tuesday and called a while ago about transmissibility. Patient reported that the patient lives with family members. The patient stated that he did not know if he had a Covid asymptomatic carrier. After a couple of weeks, we are supposed to wear a mask. Are you transmissible? The patient also stated If I was vaccinated, and I give it to someone else is it going to be a new variant. It was stated that patient never had a headache and a week later starting last night patient had headache that feels like a nail going through my head and I have soreness in my arm. My lymph nodes are tender. 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: 1360248
Sex: F
Age:
State: NV

Vax Date: 03/01/2021
Onset Date: 03/01/2021
Rec V Date: 05/29/2021
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Symptoms: Headache; tiredness; sore arm at injection site; generally feel unwell,; Chills; upset stomach; This is a spontaneous report from a contactable consumer (patient). A 59-year-old non-pregnant female patient received first dose of bnt162b2 (BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection Batch/Lot Number: EN 6198), via an unspecified route of administration, administered in Arm Left on 01Mar2021 16:30 () as 1ST DOSE, SINGLE DOSE for covid-19 immunisation. Medical history included coeliac disease, asthma, hypothyroidism, polycythaemia bradycardia from an unknown date and unknown if ongoing and Allergy to wheat, yeast, orange peel, high fructose corn syrup, material used in stress tests and wheat, yeast, orange peel, high fructose corn syrup, material used in stress tests from an unknown date and unknown if ongoing. Concomitant medication(s) included Breo, Albuterol, Synthroid, Omeprazole taken for an unspecified indication, start and stop date were not reported. On unspecified date the patient previously took morphine and experienced drug hypersensitivity. On 01Mar2021 the patient experienced headache, tiredness, sore arm at injection site, generally feel unwell, chills and upset stomach. The patient did not receive any vaccine prior four week of COVID-19 vaccination. Patient not diagnosed with COVID-19 before vaccination and since vaccination patient not tested for covid-19. Patient did not received treatment for the events. The outcome of the event was reported as recovering. No follow-up attempts are possible. No further information is expected.

Other Meds: BREO ELLIPTA; ALBUTEROL HFA; SYNTHROID; OMEPRAZOLE

Current Illness:

ID: 1360249
Sex: F
Age:
State:

Vax Date: 02/24/2021
Onset Date:
Rec V Date: 05/29/2021
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Symptoms: Headache; Shoulder was achy; Feeling wiped out; Heart palpitations; arm was really sore and this soreness went down to her elbow; she had a little headache that worsened; This is a spontaneous report from a contactable consumer (patient). A female patient (age:69; unit: unknown) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, (Batch/Lot number was not reported), via an unspecified route of administration on 24Feb2021 as 1st dose, single dose for COVID-19 immunization. The patient medical history was covid previously (Patient thought she had covid previously and wanted to know if having covid made the side effects to the vaccine worse). Patient concomitant medications were not reported. Patient stated she received the first dose of the Pfizer covid 19 vaccine on 24Feb2021. Patient did not have symptoms until 30 hours later. Patient stated she had a little headache that worsened and the second day her shoulder was achy. She reported feeling wiped out and having heart palpitations. She reported her arm was really sore and this soreness went down to her elbow. She stated she did not rest after the vaccine and wanted to know if this is what caused her to have these side effects and is it normal to have late onset of these side effects. She stated she heard the side effects to the second dose are more severe. Patient wanted to know how much she would be protected if she did not get the second dose. There was no PQC (Product quality complaint). The outcome of the events was reported as unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds:

Current Illness:

ID: 1360250
Sex: F
Age:
State: NM

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 05/29/2021
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Symptoms: 4 of 10 throbbing headache; left ear/lateral neck pain; left ear/lateral neck pain; This is a spontaneous report from a contactable other HCP reported that, A 28-year-old female (Non pregnant) patient received second dose of bnt162b2(PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: el3302), via Intramuscular route of administration in left arm on 14Jan2021 at 06:00 PM (at the age of 28-years-old) at Public Health Clinic/(Name) facility as a single dose for COVID-19immunisation. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: el1284), via Intramuscular route of administration in left arm on 23Dec2020 at 05:30 PM as a single dose for COVID-19immunisation.Patient medical history of the patient was not reported. The patient allergy history was not reported. Patient concomitant medications of the patient include ascorbic acid, betacarotene, calcium sulfate, colecalciferol, cyanocobalamin, ferrous fumarate, folic acid, nicotinamide, pyridoxine hydrochloride, retinol acetate, riboflavin, thiamine mononitrate, tocopheryl acetate, zinc oxide (PRENATAL MULTIVITAMINS) taken by mouth, once a day. It was not reported whether the patient was diagnosed covid-19 before vaccination and if tested covid-19 after vaccination. On 14Jan2021, 45 minutes after receiving her second dose of covered vaccine, presents to urgent care complaining of a 4 of 10 throbbing headache and left ear/lateral neck pain. She has not taken anything for pain, having come straight from work/vaccination clinic. She tolerated her first dose of vaccine well. Ae resulted in [Emergency room/department or urgent care]. The patient underwent lab tests and procedures which included pain assessment: 4, on 14Jan2021. Therapeutic methods were taken that include tylenol 1000mg by mouth once, patient monitoring. The outcome of all the events was recovered. No follow up attempts are possible. No further information is expected.

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

Current Illness:

ID: 1360251
Sex: M
Age:
State:

Vax Date: 02/21/2021
Onset Date:
Rec V Date: 05/29/2021
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Symptoms: Headache; Slight temperature of about 100.3 Fahrenheit; Body ache; Chills; If has side effects or needs to go tested for Covid; This is a spontaneous report from a contactable consumer (wife) reported for a male patient (Husband). A male patient of unknown age received second dose of BNT162B2 (Pfizer covid vaccine, Lot number: EN6201, Expiration date: Unknown), via an unspecified route of administration on 21Feb2021 (Sunday) afternoon as a single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. Historical vaccine included first dose of BNT162B2 (Pfizer covid vaccine) as a single dose for covid-19 immunization. On an unspecified date, patient experienced yesterday he started showing and he had a headache and a slight temperature of about 100.3 (Fahrenheit), body ache and chills. We didnt know if side effects didnt show up for like that would have been the fourth day from the time, we had the shot and this morning his chills are down, his headache is light and no temperature. Caller would like to know if it is a side effects or needs to go tested for Covid or side effect can occur after 3 or 4 days of vaccination. It was unknown if the patient received any treatment for the event. The clinical outcome of the events was unknown. No follow-up attempts are possible; information about batch/ lot number cannot be obtained.

Other Meds:

Current Illness:

ID: 1360252
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 05/29/2021
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Symptoms: tiredness; nausea; whole body was twitching; This is a spontaneous report from a contactable consumer reporting for herself. A 77-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: solution for injection, Batch/Lot number was not reported), dose 2 via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced tiredness, nausea and whole body was twitching. The outcome of the events was unknown. This Follow-up is being submitted to notify that lot/batch number is not available despite the follow-up attempts made. Follow-up attempts have been completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1360253
Sex: F
Age:
State: CA

Vax Date: 03/02/2021
Onset Date: 03/02/2021
Rec V Date: 05/29/2021
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Symptoms: Headache; fatigue; This is a spontaneous report received from a contactable consumer or other non hcp (patient). A 61-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection) dose 1 via an unspecified route of administration in Arm Left on 02Mar2021 at 09:45 am (Batch/Lot Number: en6205) as First dose, single for covid-19 immunisation. Medical history included colitis ulcerative and took ampicillin for hypersensitivity experienced rash. Concomitant medications included mesalazine, and citalopram. The patient has not taken any vaccine in four weeks. The patient has taken lialda and citalopram in two weeks. The patient has not experienced covid prior to vaccination. The patient has not tested for covid post vaccination. The patient experienced headache, and fatigue on 02Mar2021 at 19:00 pm. The patient has not taken any treatment for the events. Outcome of the events was not recovered. No follow-up attempts are possible; information about lot/batch number cannot been obtained.

Other Meds: LIALDA, CITALOPRAM

Current Illness:

ID: 1360254
Sex: F
Age:
State:

Vax Date:
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Rec V Date: 05/29/2021
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Symptoms: fatigue; This is a spontaneous report from a contactable Other-HCP. A 60-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/lot number: unknown and Expire Date: unknown), via unspecified route of administration, on an unknown date, as single dose, for Covid-19 immunisation. Medical history and concomitant medications were not reported. After vaccination, patient stated that she was having occasional fatigue. Patient did have a Covid Vaccine and the first injection she took during her on week and just had fatigue. The outcome of event was unknown. No follow-up attempts are possible. Information on Lot/Batch number has been requested. No further information is expected.

Other Meds:

Current Illness:

ID: 1360255
Sex: F
Age:
State: PA

Vax Date: 02/24/2021
Onset Date: 02/24/2021
Rec V Date: 05/29/2021
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Symptoms: Headache; Stuffiness symptoms; This is a spontaneous report from a contactable consumer. A 86-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection; Lot Number: EN6202; expiration date and NDC number were not reported) via an unspecified route of administration on 24Feb2021 at 11:50 in left arm as a single dose for COVID-19 immunization. Medical history included ongoing hypertension and ongoing hip arthroplasty. There were no additional vaccines administered on same date of the Pfizer suspect. History of all previous immunizations with the Pfizer vaccine considered as suspect was not reported as this was the first dose. The patient did not receive any prior vaccinations within 4 weeks and there were no adverse events following prior vaccinations. Investigation assessment was not provided. Patient was on other concomitant medications, but caller did not have the list to provide. As per the description, the caller reported that his aunt got the COVID vaccine on Wednesday (24Feb2021) and had headache which started half an hour after getting the shot at 12:20, and stuffiness symptoms (coded to nasal congestion) started later that evening. There was no emergency room or physician office visit. They spoke with the patient's doctor and the doctor wanted them to let us know about the events. Caller also mentioned he was wondering if there was anything that can be done to help relieve that events. The doctor suggested the patient to go and get tested for COVID. However, caller indicated the patient had not been out of the house besides going to get the shot. Patient had been quarantining in house for almost a full year and had not been going anywhere. She was deathly afraid of getting the disease. Hoping that getting the vaccine would at least allow her to go out more but do so cautiously. Caller stated he was not sure what rabbit hole the doctor was trying to go through or what was meant by the doctor recommending patient get tested for COVID. Relevant tests were not reported. The action taken with drug was unknown. The outcome of all events was not recovered. No follow-up attempts are possible; No further information is expected.

Other Meds:

Current Illness: Blood pressure high; Hip replacement

Total 2021 VAERS Injuries: 599,999

Page last modified: 03 October 2021 5:28pm