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
92,076
AK1,880
AL6,345
AR4,151
AS46
AZ14,991
CA66,887
CO12,550
CT8,943
DC1,795
DE2,009
FL42,724
FM4
GA17,031
GU124
HI2,580
IA4,919
ID2,892
IL22,128
IN24,197
KS5,047
KY9,111
LA5,500
MA15,718
MD13,434
ME3,351
MH8
MI20,971
MN13,585
MO10,747
MP30
MS3,198
MT2,477
NC18,051
ND1,501
NE3,109
NH3,218
NJ20,216
NM4,218
NV4,728
NY37,667
OH20,793
OK6,692
OR9,244
PA25,607
PR2,588
QM2
RI2,163
SC7,261
SD1,282
TN10,445
TX39,890
UT4,618
VA15,980
VI67
VT1,830
WA16,071
WI12,042
WV2,571
WY926
XB5
XL1
XV2

ID: 1106253
Sex: M
Age:
State: TX

Vax Date: 02/01/2021
Onset Date:
Rec V Date: 03/16/2021
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Symptoms: Got first vaccine 22Dec2020. After second vaccine on 01Feb2021.; Got first vaccine 22Dec2020. After second vaccine on 01Feb2021.; my hands burn all the time, at times like tonite bad enough that they keep me awake; the hands get swollen and tight to close everyday; the hands get swollen and tight to close everyday; inflammation; thesymptoms have been getting worse; red nodular areas; nodular areas/distinct nodule at the proximal ulnar aspect of my Left 4th finger; This is a spontaneous report from a contactable Physician, the patient. This is the second of two reports. The reporter describes events following both vaccinations in a vaccine series. This report is for those events which occurred following the second vaccination. A 57-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number EL3249), intramuscularly on 01Feb2021 (at the age of 57-years-old) as a single dose in the right arm for COVID-19 vaccination. Medical history included benign prostatic hyperplasia from an unknown date. The patient's historical vaccinations included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number EJ1685) on 22Dec2020 after which he experienced inflammation, joint pain and burning sensation in the joints. Prior to the vaccination, the patient was not diagnosed with COVID-19. The vaccination was administered at a hospital. Concomitant medications included acetaminophen (TYLENOL), tamulosin (MANUFACTURER UNKNOWN) and metoprolol (MANUFACTURER UNKNOWN) all from unspecified dates and for unknown indication. The patient did not receive any other vaccines within four weeks prior to the vaccination. Per the reporting physician, he got his first vaccine on 22Dec2020. His MCP and PIP joints and SI joints started burning close to 3rd week in Jan2021. He had some minor SI pains intermittently before but none with hands. Continued hurting enough that he started taking Osteobiflex and fish oil and more tylenol for inflammation. After second vaccine on 01Feb2021 the symptoms he experienced after the first dose have been getting worse. He mentioned that his hands burn all the time, at times like tonight bad enough that they keep him awake. He has red nodular areas on some of his knuckles and a distinct nodule at the proximal ulnar aspect of my left 4th finger PIP that is uniformly erythematous. Not all knuckles have the same degree of burning, but all including thumbs have it. The SI joint pain is more variable and at time does not bother him, but the hands get swollen and tight to close everyday. He plans to start some prednisone tomorrow due to the progression of the burning. The clinical outcomes of the events burning sensation in joints worsened, swelling of hands, stiffness joints, inflammation, condition worsended, erythema, nodule on extremity were reported as not recovered. The outcomes of inappropriate schedule of vaccine administration and off label use were unknown. It was also reported that since the vaccination, the patient had not been tested for COVID-19.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021154881 Same patient, same drug, different AE, different dose of vaccine.

Other Meds: TYLENOL; TAMSULOSIN; METOPROLOL

Current Illness:

ID: 1106254
Sex: F
Age:
State: NJ

Vax Date: 02/11/2021
Onset Date:
Rec V Date: 03/16/2021
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Symptoms: Severe injection site pain; fever of 101.5 for 24 hours; severe chills; body aches; migraine; This is a spontaneous report from a contactable consumer reporting for herself. A 47-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number/expiration date: not provided), via an unspecified route of administration, on 11Feb2021 at 14:00 (at the age of 47 years old) as a single dose in the left arm for COVID-19 IMMUNIZATION. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number/expiration date: not provided), via an unspecified route of administration, on an unspecified date for COVID-19 IMMUNIZATION. Relevant medical history included Epstein Barr. The patient did not have any known allergies to medications, food, or other products. The patient was not pregnant at the time of vaccination. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medication included "Fiornel" and ibuprofen (ADVIL). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On an unknown date, the patient experienced severe injection site pain, fever of 101.5 for 24 hours, severe chills, body aches and migraine. The patient received treatment for these events which included ibuprofen (ADVIL), acetaminophen, (TYLENOL) and "fiornel". The outcome of the events severe injection site pain, fever of 101.5 for 24 hours, severe chills, body aches and migraine was unknown. Since the vaccination, the patient had not been tested for COVID-19. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow-up.

Other Meds: ADVIL [IBUPROFEN]

Current Illness:

ID: 1106255
Sex: F
Age:
State:

Vax Date: 01/09/2021
Onset Date: 01/09/2021
Rec V Date: 03/16/2021
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Symptoms: lethargy; felt tired; This is a spontaneous report from a non-contactable consumer for herself. A 45-year-old female received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot/Batch number: Unknown) on 09Jan2021 via an unspecified route of administration at SINGLE DOSE for COVID-19 Immunization in the hospital. The patient's medical history and concomitant medications were not reporter. The allergies to medications, food, or other products were unknown. The patient was not pregnant at the time of vaccination. It was unknown if the patient has been tested positive for COVID-19 and if the patient was tested positive since vaccination. On 09Jan2021 the patient felt tired, lethargic all weekend. The events assessed as non-serious by the reporter. The patient did not receive any treatment. The outcome of the events was recovered on an unspecified date of Jan2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1106256
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 03/16/2021
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Symptoms: positive COVID-19 test with no symptoms; positive COVID-19 test with no symptoms.; This is a spontaneous report from a contactable consumer (patient herself). A female patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: Unknown, Expiration date: Unknown) via an unspecified route of administration on unspecified date at SINGLE DOSE for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient experienced tested for COVID-19 and found out that she was positive for the infection, positive COVID-19 test with no symptoms. The patient was supposed to have surgery but she was tested for COVID-19 and found out that she was positive for the infection, she have not had any symptoms, she did not interact with anybody and she wears double mask. The outcome of events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1106257
Sex: F
Age:
State: NC

Vax Date: 02/15/2021
Onset Date: 02/15/2021
Rec V Date: 03/16/2021
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Symptoms: exacerbated the hives; exacerbated the hives; This is a spontaneous report from a contactable consumer, the patient. A 70-years-old non-pregnant female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; lot number: EM9809), via an unspecified route of administration in the right arm on 15Feb2021 at 08:00 (at the age of 70-years-old) as a single dose for COVID-19 immunization and ampicillin (AMPICILLIN), via an unspecified route of administration from an unspecified date at an unknown dose for an unspecified indication. Ampicillin was given within two weeks of BNT162b2. Medical history included penicillin allergy and sulfa drugs allergy; all from an unspecified 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's concomitant medications were not reported. The patient did not receive any other vaccines within four weeks. The patient previously took nitrofurantoin (MACROBID) and prochlorperazine maleate (COMPAZINE); all from unknown dates to unknown dates for unknown indications and experienced allergy. The patient experienced exacerbated the hives on 15Feb2021 at 12:00. The patient had hives from ampicillin and believed that BNT162b2 exacerbated the hives. The patient went to the Emergency room/department or urgent care due to the event, exacerbated the hives. The patient received prednisone as the treatment for the event. The action taken in response to the event for ampicillin was unknown. The outcome of event, exacerbated the hives was recovering.

Other Meds:

Current Illness:

ID: 1106258
Sex: F
Age:
State: GA

Vax Date: 02/02/2021
Onset Date: 02/01/2021
Rec V Date: 03/16/2021
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Symptoms: nausea; chills; diarrhea; bad chest pain could barely breathe; bad chest pain could barely breathe; left arm where the injection was given was very painful from the injection site to her wrist and; left arm where the injection was given was very painful from the injection site to her wrist and; can barely lift her arm over her head; increase in her blood sugar; arm pain; This is a spontaneous report from a contactable consumer (patient herself). A 61-year-old female patient, not pregnant, received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL9265), via an unspecified route of administration in the left arm, on 02Feb2021 14:30, at a single dose, for covid-19 immunization. Medical history included diabetes, high blood pressure, and sciatica. Concomitant medications included insulin glargine (LANTUS); metformin; hydrochlorothiazide; candesartan; glipizide (GLIPIZIDE XL) and; colecalciferol (VITAMIN D [COLECALCIFEROL]) - all taken for unspecified indications with start and stop dates not reported. The patient previously received sitagliptin (JANUVIA) and experienced allergies. The patient did not receive any other vaccines within 4 weeks prior to the Covid vaccine. The patient did not have Covid prior vaccination. The patient received the vaccine in a public health clinic/veterans administration facility. The patient received the Pfizer vaccine dose 1 on 02Feb2021. The patient experienced nausea, chills, diarrhea and bad chest pain could barely breathe - these have passed. Her left arm where the injection was given was very painful from the injection site to her wrist and she has been alternating ice pack/heat pad and taking Tylenol 650 mg for the pain. She can barely lift her arm over her head. She also noticed an increase in her blood sugar and her blood was really dark - she stated this was unusual. She asked if there was anything she can do or take that might decrease her arm pain. All the adverse events happened on Feb2021 and resulted in doctor or other healthcare professional office/clinic visit. It was reported that the patient had not recovered from all the adverse events at the time of the report. No treatment was received for all the adverse events, except for "left arm where the injection was given was very painful from the injection site to her wrist" (alternating ice pack/heat pad and taking Tylenol 650 mg for the pain). The patient has not been Covid-tested post vaccination.

Other Meds: LANTUS; METFORMIN; HYDROCHLOROTHIAZIDE; CANDESARTAN; GLIPIZIDE XL; VITAMIN D [COLECALCIFEROL]

Current Illness:

ID: 1106259
Sex: F
Age:
State:

Vax Date: 01/30/2021
Onset Date: 02/12/2021
Rec V Date: 03/16/2021
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Symptoms: patient had the first dose of the Pfizer COVID-19 vaccine on 30Jan2021 and tested positive on 12Feb2021; patient had the first dose of the Pfizer COVID-19 vaccine on 30Jan2021 and tested positive on 12Feb2021; This is a spontaneous report from a contactable consumer via Medical information team. This consumer reported similar events for 2 patients. This is 2nd of 2 reports. A female patient (wife) of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on 30Jan2021 at single dose for COVID-19 immunization. The patient medical history was not reported. The patient's concomitant medications were not reported. The patient had the first dose of the Pfizer COVID-19 vaccine on 30Jan2021 and tested positive on 12Feb2021. The caller wanted to know whether they should repeat the dose or should they wait. The outcome of the events was unknown. Information on the lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021166986 same reporter, suspect, events, different patient

Other Meds:

Current Illness:

ID: 1106260
Sex: M
Age:
State: OH

Vax Date: 01/28/2021
Onset Date: 02/04/2021
Rec V Date: 03/16/2021
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Symptoms: Fluid from my nostrils is running constantly and it has a terrible odor when it is coming out; This is a spontaneous report from a contactable consumer (patient) for himself. A 87-years-old male patient received BNT162B2 (solution for injection, Lot number: EL9261BUD53141) via an unspecified route of administration on 28Jan2021 at single dose for COVID-19 immunisation. The patient medical history was not reported. Concomitant medications included tamsulosin at a dose of 0.4 mg, finasteride at a dose of 0.5 mg both taken for an unspecified indication and vitamin. Consumer stated, that he took first vaccination on 28Jan2021 and it's been a week now and noticed yesterday and mostly today, my fluid from my nostrils is running constantly and it has a terrible odor on 04Feb2021, when it's coming out, and again stated that, "Well, and it is reported, I don't know how I got that problem but, I mean it started after a week after getting the vaccination, there was event treatment for the event. The outcome of the event was not recovered.

Other Meds: TAMSULOSIN; FINASTERIDE

Current Illness:

ID: 1106261
Sex: F
Age:
State:

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 03/16/2021
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Symptoms: 145HR for approximately 5 minutes.; This was a spontaneous report from a contactable nurse herself (non pregnant). An 38-year-old female nurse (patient) reported received of first dose BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) via intramuscularly left arm on 05 Feb2021 09:30 am at single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient experienced 145 beats per minute Heart Rate for approximately 5 minutes on 05Feb2021 13:30. Facility type vaccine in hospital. The outcome in response to the event recovered in 2021. Information about Lot/Batch number is requested.

Other Meds:

Current Illness:

ID: 1106262
Sex: F
Age:
State: MD

Vax Date: 02/16/2021
Onset Date: 02/17/2021
Rec V Date: 03/16/2021
Hospital:

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Symptoms: Hives on side of body injection site; This is a spontaneous report from a contactable other health professional (patient). A none pregnant 30-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCIN, Solution for injection, Lot/Batch Number and Expiration Date unknown), via an unspecified route of administration, administered in right arm on 16Feb2021 at time of 13:00 (at the age of 30 years old, no pregnant at vaccination) at a single dose for COVID-19 immunization. The patient had no other medical history. No known allergies. There was no concomitant drugs. There was no other vaccine in four weeks and no other medications in two weeks. The patient did not have covid prior vaccination and did not receive covid tested post vaccination. The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCIN, lot number unknown) via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. The patient experienced hives on side of body injection site on 17Feb2021. Therapeutic measures were taken as a result of "hives on side of body injection site" and included treatment with "use of diphenhydramine (BENADRYL) and paracetamol (TYLENOL)". The outcome of event was recovering. No follow up attempts are possible. Information about Lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1106263
Sex: M
Age:
State: OH

Vax Date: 01/28/2021
Onset Date: 02/15/2021
Rec V Date: 03/16/2021
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Symptoms: Pinched nerve; Pain in his neck or shoulder; Pain in his neck or shoulder; This is a spontaneous report from a contactable consumer (patient). A 45-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number and Expiration Date were not reported), via an unspecified route of administration, on 28Jan2021, at a single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The first dose of the COVID-19 vaccine was on 28Jan2021. On 15Feb2021, the patient started experiencing pain in his neck or shoulder. On an unspecified date, the patient had pinched nerve in his neck; the patient was prescribed prednisone. They gave the patient prednisone to take but he was holding off to take prednisone because he was afraid it will hinder the immune response to the vaccine. The patient was holding off to take prednisone, but he wanted to get a professional opinion on when he should get or the time to start taking prednisone. The patient wanted to know if taking it will change the efficacy of the vaccine. The patient was asking if this would affect the vaccine's efficacy. The patient had the second dose on 17Feb2021 (day before the reporting) at 9:20 in the morning. The patient also asked if it was safe for pregnant women to get the vaccine. The outcome of the events was unknown. Information about lot number and expiration date for the suspect product will be requested in follow-up attempts.

Other Meds:

Current Illness:

ID: 1106264
Sex: M
Age:
State: OH

Vax Date: 01/29/2021
Onset Date: 02/06/2021
Rec V Date: 03/16/2021
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Symptoms: He was itching behind both ears and now it is in the crack of his butt and on his butt cheeks; It is big, welty, and red; It is big, welty, and red; Rash was reported as worsened.; Rash; This is a spontaneous report from a contactable consumer or other non hcp. A 79-year-old male patient received bnt162b2 (BNT162B2, Solution for injection, lot #: EL3302), dose 1 via an unspecified route of administration, administered in Arm Left on 29Jan2021 (Batch/Lot Number: EL3302) as SINGLE DOSE for covid-19 immunisation. Medical history included gingival disorder from an unknown date and unknown if ongoing. Concomitant medications included doxycycline hyclate (DOXYCYCLINE HYCLATE), chlorhexidine gluconate (CHLORHEXIDINE GLUCONATE) taken for gingival disorder from 21Jan2021 to 06Feb2021. On 06Feb2021, the patient experienced rash, on an unspecified date he was itching behind both ears and now it is in the crack of his butt and on his butt cheeks, it is big, welty, and red, rash was reported as worsened. The action taken in response to the event for bnt162b2 was not applicable. Therapeutic measures were taken as a result of he was itching behind both ears and now it is in the crack of his butt and on his butt cheeks (pruritus). The outcome of the events was not recovered. The outcome of the event rash was reported as worsened was unknown.

Other Meds: DOXYCYCLINE HYCLATE; CHLORHEXIDINE GLUCONATE

Current Illness:

ID: 1106265
Sex: F
Age:
State: MI

Vax Date: 02/02/2021
Onset Date: 02/02/2021
Rec V Date: 03/16/2021
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Symptoms: Nausea; Chills; This is a spontaneous report from a contactable consumer (patient). A 79-year-old female patient received the first dose of BNT162B2 (BNT162B2, lot number and expiry date were unknown), via an unspecified route of administration on 02Feb2021 at a single dose on the left arm for COVID-19 immunization. Medical history included ongoing stage 4 lung cancer from Dec2019 and chemo from Apr2020. The patient had no concomitant medications. On 02Feb2021, the patient experienced nausea and chills. The patient reported that she had her first Pfizer shot on 02Feb2021. She had just a few problems in the middle of night afterwards- nausea and chills. That night she had nausea and chills. It lasted for about 30 minutes. She just laid in bed. She was fine after that and was fine the next morning. Outcome of the events was recovered on 02Feb2021. Information on the Lot/Batch Number has been requested.

Other Meds:

Current Illness: Lung cancer stage IV

ID: 1106266
Sex: M
Age:
State:

Vax Date: 02/03/2021
Onset Date: 02/01/2021
Rec V Date: 03/16/2021
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Symptoms: tired; lightheaded; This is initial spontaneous report from a contactable consumer (patient himself). A male patient of unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection) via an unspecified route of administration on 03Feb2021 at single dose for COVID-19 immunization. Medical history and Concomitant medications were not reported. Patient received the COVID-19 vaccine last Wednesday on 03Feb2021. He was fine for a few days after it and then starting about 2 days ago and including today, he had become quite tired in Feb2021. He had been a little lightheaded (Feb2021) but more so very tired. The outcome of the events was unknown. Information on the Lot/Batch Number has been requested.

Other Meds:

Current Illness:

ID: 1106267
Sex: F
Age:
State: NJ

Vax Date: 02/04/2021
Onset Date: 02/08/2021
Rec V Date: 03/16/2021
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Symptoms: I had a swollen lymp node in my left armpit; This is a spontaneous report from a contactable consumer (patient). A 56-year-old female patient reported that first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot# EL9264), via unspecified route of administration on 04Feb2021 13:45 at single dose in the left arm for covid-19 immunization. Medical history included hypertension. Concomitant medications included Lycortin, Norvasc, Carvedilol, Aspirin, Doxycycline. The patient reported as, I had a swollen lymp node in my left armpit on 08Feb2021. Outcome of the event was not recovered.

Other Meds: ASPIRIN [ACETYLSALICYLIC ACID]; CARVEDILOL; DOXYCYCLINE; LYCORTIN-S [HYDROCORTISONE]; NORVASC

Current Illness:

ID: 1106268
Sex: F
Age:
State: IL

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 03/16/2021
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Symptoms: Nausea; Diarrhea; Fever; This is a spontaneous report from a contactable consumer (patient). A 67-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EM9810), via an unspecified route of administration on 05Feb2021 at a single dose on left arm for COVID-19 immunisation. Medical history was not reported. There were no concomitant medications. The patient was asking if Pfizer had people, about 3 or 4 days later, get nausea and diarrhea after getting the COVID shot. She had a real bad fever 3 hours after the shot but felt fine the next day. But now she has nausea and diarrhea that started yesterday (08Feb2021). She normally does not that have that. Her nausea has improved because she took a nausea pill, ondansetron (ZOFRAN) 2 mg. Therapeutic measures were taken as a result of nausea. The outcome of the event fever was recovered on 06Feb2021, nausea was recovering, and diarrhea was recovered on 09Feb2021.

Other Meds:

Current Illness:

ID: 1106269
Sex: M
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 03/16/2021
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Symptoms: Blood sugar spiked; This is a spontaneous report from a non-contactable consumer. A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Lot Number and Expiration Date were not reported), via an unspecified route of administration, on an unspecified date, at a single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, blood sugar spiked after getting the vaccine. The patient was brought to the emergency room (ER) to stabilize blood sugar level and went home after. The adverse event resulted in emergency room/department or urgent care. The outcome of the event was unknown (as reported). No follow-up attempts are possible; information about batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1106270
Sex: F
Age:
State: CA

Vax Date: 02/13/2021
Onset Date: 02/13/2021
Rec V Date: 03/16/2021
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Symptoms: I feel so tired; a little bit dizzy; Intravenous administration; This is a spontaneous report from a contactable consumer (patient) via a Pfizer-sponsored program. This female consumer of unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; lot number unknown) intravenously on 13Feb2021 as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. On unspecified dates the patient reported she felt so tired and a little bit dizzy. The clinical outcomes of she felt so tired and a little bit dizzy were unknown. The clinical outcome of intravenous administration was recovered on 13Feb2021. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1106271
Sex: M
Age:
State: NY

Vax Date: 02/05/2021
Onset Date: 02/12/2021
Rec V Date: 03/16/2021
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Symptoms: "Caller got his 1st dose a week ago (05Feb2021) and was tested positive of Covid-19 today/He had symptoms like headache, fever"; This is a spontaneous report from a Pfizer-sponsored program via a contactable consumer (patient). A 29-years-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, NDC number, UPC number, Batch/Lot number, Expiry date: unknown), via an unspecified route of administration on 05Feb2021 at single dose for covid-19 immunisation. Covid19 vaccine was a Pfizer product. Covid19 vaccine manufacturer was unspecified. Relevant medical history and concomitant medications were reported None. The patient got his 1st dose a week ago (05Feb2021) (reported as 8 days after the first dose) and was tested positive for Covid today (12Feb2021). His 2nd dose was on 28Feb2021. The patient stated, "I do not have that card." Investigation assessment was no. Patient was already negative in 2021. The patient underwent lab tests and procedures which included SARS-CoV-2 test and results were positive (drug ineffective) on 12Feb2021. The outcome of event positive COVID-19 was recovered in 2021. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1106272
Sex: F
Age:
State: AZ

Vax Date: 02/02/2021
Onset Date: 02/01/2021
Rec V Date: 03/16/2021
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Symptoms: she felt tired; red circle on the injection area that starts to get bumpy; red circle on the injection area that starts to get bumpy; This is a spontaneous report from a Pfizer-sponsored program COVAX US Support. A contactable consumer (patient) reported this female patient of unspecified age received dose 1 of BNT162B2 (PFIZER BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 02Feb2021 as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. On an unspecified date in Feb2021 the patient felt tired and experienced a red circle on the injection area that started to get bumpy. The outcomes of tired and red circle on the injection area that started to get bumpy were unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow-up.

Other Meds:

Current Illness:

ID: 1106273
Sex: F
Age:
State: NY

Vax Date: 02/04/2021
Onset Date: 02/01/2021
Rec V Date: 03/16/2021
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Symptoms: Pain at the injection site.; This is a spontaneous report from a Pfizer-sponsored program, received from a contactable consumer (patient's daughter), reporting for a patient (Mother). A female patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number unknown), via an unspecified route of administration on 04Feb2021 as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. On an unknown date in Feb2021 the patient experienced pain at the injection site. The clinical outcome of the pain at the injection site was unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1106274
Sex: M
Age:
State: CO

Vax Date: 02/17/2021
Onset Date: 02/17/2021
Rec V Date: 03/16/2021
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Symptoms: My Sugar level have shot up very high. It is not going below 250 and goes to 390 after eating!; This is a spontaneous report from a contactable consumer (patient). A 65-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered at the left arm on 17Feb2021 16:15 at single dose for COVID-19 immunization. Medical history included ongoing diabetes mellitus (diabetic). Concomitant medications were none. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was vaccinated at a pharmacy or drugstore. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19. On 17Feb2021, the patient's sugar level had shot up very high. It was not going below 250 and went to 390 after eating. No therapeutic measure was taken as a result of the event. Clinical outcome of the event was not recovered. Information on the lot/batch number has been requested.

Other Meds:

Current Illness: Diabetic

ID: 1106275
Sex: M
Age:
State: MI

Vax Date:
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Rec V Date: 03/16/2021
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Symptoms: sciatic nerve pain; This is a spontaneous report from a contactable consumer (patient). An 83-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration on an unspecified date (Batch/Lot Number: EL9261; Expiration Date: May2021) at single dose, second dose via an unspecified route of administration on an unspecified date (Batch/Lot Number: EL9267; Expiration Date: May2021) at single dose for COVID-19 immunization. There was no medical history reported. There were no concomitant medications. Patient is calling about the second vaccination he had for the virus and he developed sciatic nerve pain and he wanted to know if it was safe to take Ibuprofen with having gotten the vaccine or if that would hurt his protection from the virus. He confirmed it is the Pfizer COVID 19 vaccine. He also said with the sciatic nerve pain he actually got the first vaccination and then he was messing around putting in light bulbs and stuff and that is when he got the sciatic nerve pain from an unspecified date so it had been a couple weeks or so. He didn't think it was from the vaccination. He kept hearing it on TV about taking Tylenol and everything with the vaccine. No further information provided. He clarified he was retired from company and he is no longer an employee there. The outcome of the event was unknown.; Sender's Comments: Based on the implied time association, the possible contribution of suspect vaccine BNT162B2 to the event sciatic nerve pain cannot be totally excluded. The concurrent condition reported as "he was messing around putting in light bulbs and stuff and that is when he got the sciatic nerve pain from an unspecified date " may be major cofounder.

Other Meds:

Current Illness:

ID: 1106276
Sex: F
Age:
State: NC

Vax Date: 02/11/2021
Onset Date: 02/14/2021
Rec V Date: 03/16/2021
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Symptoms: Shingles; This is a spontaneous report from a contactable consumer or other health professional. A 28-years-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Manufacturer: Pfizer/BioNTech; Lot: EN5318) via an unspecified route of administration on 11Feb2021 in Arm Right at single dose for COVID-19 immunisation. Medical history included asthma, seasonal allergy (seasonal allergies) from an unknown date and unknown if ongoing. Historical vaccination included at age of 28 years first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Manufacturer: Pfizer/BioNTech; Lot: EL3247) on 21Jan2021 in Left arm at single dose for COVID-19 immunisation. Concomitant medications included cetirizine and fluticasone propionate (FLONASE) taken for an unspecified indication, start and stop date were not reported. On 14Feb2021, The patient experienced shingles. The action taken in response to the event for BNT162B2 was not applicable. Therapeutic measures were taken as a result of shingles. The outcome of event was recovering.

Other Meds: CETIRIZINE; FLONASE

Current Illness:

ID: 1106277
Sex: M
Age:
State:

Vax Date: 02/12/2021
Onset Date: 02/12/2021
Rec V Date: 03/16/2021
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Symptoms: Sore arm at injection site; Joint pain in my knees; Tiredness and fatigue.; This is a spontaneous report from a non-contactable consumer, the patient. A 28-years-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot Number EL3247) via an unspecified route of administration, administered in Arm Left on 12Feb2021 at 11:30 (at the age of 28-years-old) as SINGLE DOSE for covid-19 immunization. Facility in which vaccine was administered was a Workplace clinic Medical history included Known allergies: Penicillin. Concomitant medication included paracetamol (TYLENOL). Historical Data includes BNT162B2 Dose 1, Lot number: EL3247, Administered on 22Jan2021 at 12:00, in the Left arm for covid-19 immunization. No other vaccines were given within 4 weeks. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination the patient had not been tested for COVID-19. On 12Feb2021 at 16:00 The patient experienced sore arm at injection site, joint pain in my knees, tiredness and fatigue. The events were considered non serious. No treatment was given for the events. The clinical outcome of the events sore arm at injection site, joint pain in my knees, tiredness and fatigue were recovering. No follow up attempts are possible. No further information is expected.

Other Meds: TYLENOL

Current Illness:

ID: 1106278
Sex: F
Age:
State:

Vax Date: 02/05/2021
Onset Date: 02/12/2021
Rec V Date: 03/16/2021
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Symptoms: severe itching and a red rash across a large area in my mid back area; severe itching and a red rash across a large area in my mid back area; This is a spontaneous report from a non-contactable consumer (patient). This 68-year-old female patient received dose 2 of BNT162B2 (PFIZER BIONTECH COVID-19 VACCINE; lot number El9265) via an unspecified route on 05Feb2021 at 11:30 (at the age of 68-years-old) as a single dose in the left arm for COVID-19 immunization. Medical history was not reported. The patient was not pregnant at the time of vaccination. The patient was not diagnosed with COVID-19 prior to vaccination. The patient did not receive any other vaccines within 4 weeks prior to the vaccine. Concomitant medications were not reported. The patient previously received dose 1 of BNT162B2 (lot number EL1283) on 15Jan2021 at 19:15 in the left arm for COVID-19 immunization. The patient previously received sulfa drugs from an unknown date for an unknown indication and experienced allergy. On 12Feb2021, the patient experienced severe itching and a red rash across a large area in her mid back area. The patient did not receive any treatment for the events. The outcome of severe itching and red rash across a large area in her mid back area was not recovered. It was also reported that since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Other Meds:

Current Illness:

ID: 1106279
Sex: F
Age:
State: MN

Vax Date: 01/26/2021
Onset Date: 01/27/2021
Rec V Date: 03/16/2021
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Symptoms: Prolonged tiredness; increased weakness; dragging right foot when walks; little more trouble swallowing pills than before; little more trouble swallowing pills than before; This is a spontaneous report from a contactable consumer (the patient). A 93-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number EL1283), via an unspecified route of administration in the right arm on 26Jan2021 09:15 (at the age of 93-years-old) as a single dose for COVID-19 immunization. The patient's medical history included: aortic stenosis, COPD (chronic obstructive pulmonary disease), blood pressure medications, and trouble swallowing pills. The patient was not pregnant at the time of vaccination. The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient had unspecified concomitant medications. The patient did not receive any other vaccines within four weeks prior to the vaccination. On 27Jan2021, the patient experienced prolonged tiredness, increased weakness, dragging right foot when walks, little more trouble swallowing pills than before. No treatment was received for the events. The clinical outcome of the event was not recovered. It was also reported that since the vaccination, the patient had not been tested for COVID-19.

Other Meds:

Current Illness:

ID: 1106280
Sex: U
Age:
State: AL

Vax Date:
Onset Date:
Rec V Date: 03/16/2021
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Symptoms: It was almost like I had no control of my body; I was like walking forward I couldn't stop myself; it's almost like I have been pushed like into the window braced myself it scared me; my arm of course they gave me the shot I couldn't even brush my teeth/my arm didn't hurt till I woke up in the middle of the night; I couldn't even brush my teeth this morning; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date not reported), via an unspecified route of administration, administered in arm on an unspecified date as single dose for COVID-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient had the vaccine at 3 O'clock and had no reaction, didn't feel anything had no reaction so the patient went to bed around 8:30 or 9 and watched TV for some time and sleep around 10:30, woke up at 2:30 because of the bathroom and weirdest thing the patient stood up and didn't feel dizzy but went to turn the TV off and it was almost like the patient had no control of the body was like walking forward and couldn't stop, it's almost like the patient has been pushed like into the window braced self, and it scared the patient. The patient sat on the table and was going to the bathroom and stood up and same thing happened, could see the opening of the bathroom of course but the body did the same thing it was like the patient has not control and kind of falling towards the lift. The patient went into the kitchen to get the information from the hospital where the vaccine was administered, to see if the patient got the number to call and it happened again it hasn't happened since but didn't know all the number, tried to call and didn't know how serious that was. The patient tried to call the hospital back but it kind of worried the patient because this is kind of (incomplete sentence) and then patient's arm of course they gave the shot, the patient couldn't even brush my teeth this morning but that's kind of expected when you get this type of a shot sometimes so that was not concerning me, the only thing that said on the paper was dizziness and this may be a form of dizziness but the patient wasn't feeling dizzy though my head wasn't spinning. The patient didn't know how serious this may or may not be and how long it lasts. That's okay, that's nobody's fault, the patient just didn't know what to do how serious, that a reaction the patient was assuming. The patient further stated that like motor skills are (incomplete sentence), honestly it was like the patient was a little drunk like, was staggering and couldn't control the body, was awake for 8 hours after the shot and nothing was going on and the arm wasn't hurting either, arm didn't hurt till waking up in the middle of the night. The patient was asking if this was a serious side effect and that the patient should not get the second shot. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1106281
Sex: F
Age:
State:

Vax Date: 02/10/2021
Onset Date: 02/11/2021
Rec V Date: 03/16/2021
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Symptoms: Been feeling unwell for more than 24 hours. Very fatigued and this is day 3; Been feeling unwell for more than 24 hours. Very fatigued and this is day 3; This is a spontaneous report from a non-contactable consumer (patient). A 30-year-old non-pregnant female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; solution for injection) via an unspecified route of administration in the left arm on 10Feb2021 (at the age of 30-years-old) as a single dose for COVID-19 immunization. Medical history was not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications ("other medications in two weeks") were reported as none. The patient previously received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; solution for injection) via an unspecified route of administration in the right arm on 24Jan2021 (at the age of 30-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. On 11Feb2021 the patient experienced "been feeling unwell for more than 24 hours. Very fatigued and this is day 3." The patient did not receive treatment for the adverse events. The clinical outcome of the events "been feeling unwell for more than 24 hours. Very fatigued and this is day 3" were recovering/resolving. It was also reported that since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1106282
Sex: F
Age:
State: NY

Vax Date: 01/14/2021
Onset Date: 01/14/2021
Rec V Date: 03/16/2021
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Symptoms: On her right inner wrist area she developed a hive; This is a spontaneous report from a contactable consumer (patient's husband). A 75-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 14Jan2021 (batch/lot number: EL8982) at a single dose for COVID-19 immunisation. The patient had no medical history. There were no concomitant medications. The first experience was with the first dose. On her right inner wrist area, she developed a hive, just one. The hive appeared a couple hours after the first vaccine. The hive stayed there for 3 to 4 hours and then dissipated. Outcome of the event was recovered on 14Jan2021.

Other Meds:

Current Illness:

ID: 1106283
Sex: F
Age:
State:

Vax Date: 02/06/2021
Onset Date: 02/01/2021
Rec V Date: 03/16/2021
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Symptoms: completely lethargic; couldn't move; headache; pain in her joints; fatigued; slightly elevated fever like over 99 less than 100; sugar has been elevated and it's spiking up and down; This is a spontaneous report from a contactable consumer (daughter). A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot EL8982, second dose) solution for injection on 06Feb2021 at 16:00 (at an unknown age) as a single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. Historical vaccine included BNT162B2 (Lot EL8982, first dose) for COVID-19 immunisation on 16Jan2021 and experienced shaking and pain in your arm. The patient had the second shot on Saturday, 06Feb2021, and at 8pm she had a headache, pain in her joints, was fatigued, had a slightly elevated fever like over 99 less than 100. Then on 07Feb2021, she could not get out of bed, completely lethargic, fatigued, couldn't move really was in bed for almost a full day and a half. Now the concern was her sugar has been elevated and it's spiking up and down this entire week in Feb2021. The outcome of the events headache, pain in her joints, fatigued, fever, completely lethargic, couldn't move and blood sugar level fluctuation was unknown.

Other Meds:

Current Illness:

ID: 1106284
Sex: F
Age:
State:

Vax Date: 01/30/2021
Onset Date: 01/30/2021
Rec V Date: 03/16/2021
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Symptoms: No taste; Migraine; Fever; This is a spontaneous report from a non-contactable consumer (patient herself). A 45-year-old non-pregnant female patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/lot number: Unknown and Expiration date: Unknown), via an unspecified route of administration on 30Jan2021 (at the age of 45-year-old) at single dose for COVID-19 immunisation in hospital. The patient's medical history was unknown. It was unknown whether the patient had allergies to medications, food, or other products or not. Concomitant medications were not reported. The patient previously received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/lot number: Unknown and Expiration date: Unknown), on 09Jan2021 (at the age of 45-year-old) at single dose for COVID-19 immunisation and felt tired, lethargic all weekend. It was unknown whether the patient received any other vaccines within 4 weeks prior to the COVID vaccine or not. The patient was not diagnosed with COVID-19 prior to vaccination. It was unknown whether the patient has been tested for COVID-19 since the vaccination or not. On 30Jan2021, the patient experienced no taste, fever and migraine. The patient underwent lab tests and procedures included body temperature: Fever on an unspecified date. The events were considered as non-serious by the consumer. No treatment received for the adverse events. The outcome of the events was recovered on an unspecified date in 2021. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1106285
Sex: M
Age:
State: AZ

Vax Date: 02/17/2021
Onset Date: 02/17/2021
Rec V Date: 03/16/2021
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Symptoms: side effect of blood sugar; This is a spontaneous report from a contactable consumer (patient). A 66-year-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9267, expiry date not reported), via an unspecified route of administration at the right arm on 17Feb2021 at single dose for COVID-19 immunization. Medical history included hypertension (blood pressure high) from Jan2019 and diabetes mellitus (diabetic) from Apr2019. The patient experienced side effect of blood sugar on 17Feb2021. Patient said he tested his blood sugar before he got the vaccine in the morning before breakfast it was 95, which was normal for him, then his blood sugar was lower than normal after breakfast which he got at a restaurant he goes to regularly so he knew how it usually would be, by 30 points. He said that he keeps good enough records to tell that after lunch, which was a meal he eats regularly so he should know what his sugar usually is, and his sugar was 65 points higher, then after his evening meal it was 10 points higher. He clarified that he got his first dose of the vaccine before he ate breakfast. Clinical outcome of the event was unknown.

Other Meds:

Current Illness:

ID: 1106286
Sex: F
Age:
State: FL

Vax Date: 02/19/2021
Onset Date: 02/19/2021
Rec V Date: 03/16/2021
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Symptoms: pinching all over body; mildly nauseated; Plantar fasciitis; The pain in my foot became excruciating; could barely walk; The pain in my foot became excruciating; could barely walk; This is a spontaneous report from a contactable Consumer (patient). A 67-year-old female patient received second dose bnt162b2 (PFIZER COVID 19 VACCINE, lot number= EL9263), via an unspecified route of administration in right arm on 19Feb2021 09:30 AM at single dose for COVID-19 immunization. Medical history included known allergies to Sulfites, Iodine as contrast, Dairy, Gluten. Concomitant medication included levothyroxine, liothyronine (NP THYROID), latanoprost (LATANOPROST) and Supplements (Other medications in two weeks). The patient was not pregnant. The patient did not have COVID prior vaccination. The patient did not have COVID tested post vaccination. The patient received first dose bnt162b2 (PFIZER COVID 19 VACCINE, lot number= COVID-19 immunization), via an unspecified route of administration in right arm on 29Jan2021 11:30 AM at single dose for COVID-19 immunization. The patient did not have other vaccine in four weeks. 19Feb2021 after 2nd shot: pinching all over body and mildly nauseated. Plantar fasciitis left foot had no pain for 24 hours. 24 hours later: no nausea. The pain in the foot became excruciating; could barely walk. Lasted 2 days. Milder now. Adverse event start date was 19Feb2021 10:30 AM. The outcome of the events was recovering.

Other Meds: NP THYROID; LATANOPROST

Current Illness:

ID: 1106287
Sex: M
Age:
State: GA

Vax Date: 02/24/2021
Onset Date: 02/24/2021
Rec V Date: 03/16/2021
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Symptoms: diarrhea worsened 2 hours after receiving the vaccine; Ringing in my ear; was already having a flare; Hearing loss was already there and the vaccine actually exacerbated the situation; This is a spontaneous report from a contactable consumer, the patient. A 50-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot EN6201, first dose) solution for injection intramuscular in the right arm on 24Feb2021 at 17:00 (at the age of 50-years-old) as a single dose for COVID-19 vaccination. Medical history included ongoing irritable bowel syndrome from Mar2020 and acid reflux (esophageal). Concomitant medication included ongoing lansoprazole (PREVACID) for acid reflux (esophageal) from Nov2020. The patient stated his diarrhea worsened 2 hours after receiving the vaccine (24Feb2021 at 19:00) and had diarrhea again around 10 pm. The patient stated hearing loss was already there and the vaccine actually exacerbated the situation in 2021. The patient also experienced ringing in my ear in 2021. The patient's nurse, primary care doctor, and gastroenterologist stated it was okay to receive the vaccine as the patient was in the middle of a flare up with his IBS (inflammatory bowel syndrome) in 2021. Treatment for the event hearing loss exacerbated included unspecified steroids and has been working. The outcome of the events diarrhea worsened and ringing in my ear was unknown. The outcome of the events hearing loss exacerbated and having a flare was recovering.

Other Meds: PREVACID

Current Illness: Irritable bowel syndrome

ID: 1106288
Sex: M
Age:
State: SC

Vax Date: 02/18/2021
Onset Date: 02/18/2021
Rec V Date: 03/16/2021
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Symptoms: experienced a lot of pain; had trouble trying to breathe; sweating; fever; couldn't move his arm it hurt so much; couldn't move his arm it hurt so much; I don't feel right/he is not himself at all; I feel sick; nauseous; horrible headache; both his eyes were black and blue; part of the shoulder she put it in was swollen; I have to give him something with sugar to get it back up; instead of going through the muscle that you supposed to,she went through his shoulder, she did it on his shoulder; This is a spontaneous report received from a contactable consumer (patient's wife). A male patient of an unspecified age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN6200, expiry date: unknown), via an unspecified route of administration in the shoulder (as reported), on 18Feb2021, as single dose, for COVID-19 immunisation. Medical history included ongoing diabetes mellitus (reported as diabetic). The patient's concomitant medications were not reported. Historical vaccine included the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiry date unknown), via an unspecified route of administration in the left arm, on an unspecified date, as single dose, for COVID-19 immunisation. On 18Feb2021, the patient received his second shot. It was reported that when the patient was given the injection, instead of going the muscle that you supposed to, the girl went through his shoulder, she did it on his shoulder. It did not bother the patient and when they got home, all of a sudden, on the same day (18Feb2021), the patient experienced a lot of pain, had trouble trying to breathe, was sweating, had a fever which went down after taking Tylenol, couldn't move his arm it hurt so much. During the night of 18Feb2021, it was reported that the patient said, "I don't feel right, I feel sick", he was nauseous, and he was not himself at all. On 18Feb2021, the patient also had a horrible headache, his eyes were black and blue (pending clarification), and the part of the shoulder she put it in was swollen. It was reported that the patient is diabetic, and the patient's wife stated "I have to give him something with sugar to get it back up". It was reported that the patient never had anything like this before. Treatment included Tylenol for fever. The patient was recovering from fever. The outcome of the remaining events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness: Diabetic

ID: 1106289
Sex: F
Age:
State: DE

Vax Date: 02/17/2021
Onset Date: 02/17/2021
Rec V Date: 03/16/2021
Hospital: Y

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Symptoms: nausea; violent headache; chills/shivering; vomiting; cannot sleep; having vivid dreams; trouble thinking; This is a spontaneous report from a contactable consumer (patient) via a Pfizer-Sponsored Program. An 80 (units not provided) female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 17Feb2021 (at the age of 80, units not provided) as a single dose for COVID-19 immunization. Medical history and concomitant medications were not reported. On 17Feb2021 the patient experienced nausea, violent headache, chills/shivering, vomiting, cannot sleep, having vivid dreams and trouble thinking. It was reported that the patient was hospitalized in the ER (emergency room) 45 minutes after receiving the dose. The clinical course was reported as follows: "The patient received her first COVID-19 vaccine and ended up in the ER with a violent headache, nausea, chills, shivering, trouble thinking and even sleep was an enemy because she had vivid dreams." The patient reported that due to these symptoms she was thinking to get the second dose later than 3 weeks. She wanted to know if she should get the second dose. She also wanted to know if she could pass these side effects along (as reported). The clinical outcomes of the events nausea, violent headache, chills/shivering, vomiting, cannot sleep, having vivid dreams and trouble thinking were all unknown. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds:

Current Illness:

ID: 1106291
Sex: M
Age:
State: WA

Vax Date: 02/15/2021
Onset Date: 02/01/2021
Rec V Date: 03/16/2021
Hospital: Y

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Symptoms: small ischemic stroke; elevated white blood count; fever; body aches; chills; headache; This is a spontaneous report from a contactable consumer (patient). A 68-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Lot number EL9269, expiration date May2021), via an unknown route of administration on 15Feb2021 (at the age of 68-years-old) as a single dose in the left arm for COVID-19 Prevention/ immunization. The patient's medical history included a dental procedure on 18Feb2021 for a cracked tooth from an unknown date. The patient received procaine hydrochloride (NOVOCAIN) on 18Feb2021 for the dental procedure. On 18Feb2021 the patient experienced fever, body aches, chills, and a headache; and on an unknown date in Feb2021 the patient experienced a small ischemic stroke. The patient was hospitalized for the ischemic stroke on 19Feb2021. The patient underwent lab tests and procedures which included a Magnetic resonance imaging (MRI) of the brain on 20Feb2021 which showed a small ischemic stroke and white blood cell count which was elevated (in the low 20s) on 19Feb2021 and on 20Feb2021, white blood cell count was normal. Therapeutic measures were taken as a result of the ischemic stroke which included Plavix. The clinical outcome of the ischemic stroke was unknown; fever, body aches and chills were recovered on 19Feb2021; white blood cell count increased recovered on 20Feb2021; headache was not recovered. The patient was hospitalized for three days. The patient mentioned that he was not associating the stroke with the vaccine but rather associates it with the added stress on his body.

Other Meds: NOVOCAIN

Current Illness:

ID: 1106292
Sex: F
Age:
State: GA

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 03/16/2021
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Symptoms: BP 142/68; like my throat is closing up; Voice hoarse; chest feeling tight; This is a spontaneous report from a contactable pharmacist. A 67-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot number: EL9265), via an unspecified route of administration on 05Feb2021 at a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took sulfamethoxazole, trimethoprim (BACTRIM) and flu vaccine and experienced allergies. The patient was vaccinated on 05Feb2021. Patient was initially hesitant to get vaccine, reported prior bad reaction to flu vaccine. Patient spoke with the pharmacist and decided to proceed with vaccination. On 05Feb2021, approximately 2 minutes after being seated in the observation area, patient began to feel "like her throat was closing up". Another employee brought the attention of this RN who notified the pharmacist and other clinic staff. Initial assessment, patient seated, in apparent distress stating, "I feel like my throat is closing up". Voice hoarse. 25 mg diphenhydramine hcl (BENADRYL) administered. Patient declined additional 25 mg diphenhydramine hcl stating it made her too sleepy. Patient brought to private monitoring area. VS obtained. HR 78, BP 130/73, SpO2 99%. Reported feeling "some better". HR 76, SpO2 97%, BP 106/66; reported "chest feeling tight". Decision for epinephrine (Epi) administration. Epi Pen administered to L thigh. HR 89, BP 142/68, SpO2 99%. Patient taken to emergency department (ED). Care tx ED RN. Patient stable upon tx to ED. The patient required emergency room/department or urgent care. Therapeutic measures were taken as a result of the events which included diphenhydramine hcl and epinephrine. The outcome of the events was unknown.; Sender's Comments: Based on a close chronological connection to the vaccine a causal relationship between reported events and BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1106293
Sex: M
Age:
State:

Vax Date: 02/25/2021
Onset Date: 02/01/2021
Rec V Date: 03/16/2021
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Symptoms: sore arm; This is a spontaneous report from a contactable consumer, the patient. An 86-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Lot number: not reported), via an unspecified route of administration on 25Feb2021 as a single dose for COVID-19 immunization; and apixaban (ELIQUIS), at an unspecified dose, frequency, route of administration and dates of use for blood thinner. Medical history included blood thinner therapy from an unknown date and unknown if ongoing; the patient had no allergies. Concomitant medications were not reported. On an unspecified date in Feb2021, the patient experienced a sore arm. The patient stated that he noted that the paperwork stated to tell the nurse if you were taking a blood thinner, he took apixaban, but no one asked him about that. The patient wondered if there was known information about apixaban with the vaccination. The action taken in response to the event for apixaban was unknown. The clinical outcome of sore arm was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained. Follow-Up (26Feb2021): This is a follow-up report based on information received by Pfizer from [manufacturer control number [COMPANY--2021-021398], license party for apixaban (ELIQUIS) and includes: License Partner Assessment. Assessment: For Eliquis (Unknown), the reporter did not provide any causality assessments. Further company follow-up with the Consumer is not possible. Sore Arm was non-serious and related to apixaban

Other Meds:

Current Illness:

ID: 1106294
Sex: F
Age:
State: IL

Vax Date: 02/23/2021
Onset Date: 02/24/2021
Rec V Date: 03/16/2021
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Symptoms: I had periods of dizziness like my atrial fibrillation was acting up every few minutes all day, both days; Left arm was sore for a day; I had periods of dizziness; I was fatigued and took 2 naps each day; This is a spontaneous report from a contactable consumer (patient herself). An 84-year-old female patient received BNT162B2 (Pfizer-BioNTech COVID-19 mRNA vaccine, Lot number: EN6200), via an unspecified route of administration on the left arm, first dose on 23Feb2021 12:15 at single dose for COVID-19 immunization. Medical history included atrial fibrillation from an unknown date and allergies to penicillin. The patient is not pregnant. No other vaccine received in four weeks. Concomitant medication included cyanocobalamin (B12-VITAMIIN), vitamin b complex (B COMPLEX), calcium (CALCIUM), ascorbic acid (VIT C), and rivaroxaban (XARELTO) from unspecified dates in two weeks. On 24Feb2021, the patient experienced left arm was sore for a day however the day following the vaccination and the day after that (Wed and Thursday) patient had periods of dizziness like her atrial fibrillation was acting up every few minutes all day, both days. Patient was fatigued and took 2 naps each day. No treatment was received for the AEs. Patient did not have COVID prior vaccination and not tested with COVID post vaccination. The outcome of the event left arm was sore for a day was recovered on 25Feb2021, and for the other events, it was unknown.

Other Meds: B12-VITAMIIN; B COMPLEX [VITAMIN B COMPLEX]; CALCIUM; VIT C; XARELTO

Current Illness:

ID: 1106295
Sex: F
Age:
State: IL

Vax Date: 02/17/2021
Onset Date: 02/27/2021
Rec V Date: 03/16/2021
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Symptoms: fever; I have dystonia (OMD)/ my symptoms have been aggravated the last few days; I have dystonia (OMD)/ my symptoms have been aggravated the last few days; This is a spontaneous report from a contactable consumer (patient). A 66-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in arm left on 17Feb2021 16:45 (batch/lot number: EN 6200) as a single dose for COVID-19 immunisation. Medical history included dystonia (OMD), multi nodular goiter, fatty liver, and uterine fibroids. The patient was not pregnant at the time of vaccination. Concomitant medications included omeprazole, colecalciferol (VITAMIN D), and tonic lemonade with thc; taken for unspecified indications, start and stop dates were not reported. The patient previously took amoxicillin clavulanate and experienced allergies. On 27Feb2021 16:00, the patient has just developed a fever and she really doesn't get fevers. She was normally low at 96.7 and today she was 98.7. She has dystonia (OMD) and her support group was reporting Covid vaccines were making dystonia symptoms worse. Her symptoms have been aggravated the last few days. She had no dystonia reaction until the last 2 days and symptoms might not have anything to do with the vaccine. She was just reporting this because her support group was saying they were worse since the vaccine. She was concerned she has a fever since she never gets them. She hasn't been out of the house since the vaccination. Facility type for the vaccine was a school or student health clinic. No other vaccine in four weeks. No Covid prior to vaccination and was not Covid tested post vaccination. There was no treatment received for the events. The outcome of the events was unknown.

Other Meds: OMEPRAZOLE; VITAMIN D [COLECALCIFEROL]

Current Illness:

ID: 1106296
Sex: F
Age:
State: MA

Vax Date: 02/24/2021
Onset Date: 02/26/2021
Rec V Date: 03/16/2021
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Symptoms: hearing loss in left ear; tinnitus; This is a spontaneous report from a contactable consumer (patient). A 82-year-old female patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE) (lot number/expiration date: unknown), on 24Feb2021 (at the age of 82 years old) as a single dose in the left arm for COVID-19 immunization. Relevant medical history included known allergies: Keflex. Historical vaccine included: first dose of BNT162B2 lot number=en9581, administration date=03Feb2021 at 02:00 PM, Right arm. Prior to the vaccination, the patient was not diagnosed with COVID-19. Concomitant medications included warfarin sodium (WARFIN), Spironolactone, Torsemide. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 26Feb2021at 14:00 AM, the patient experienced Hearing loss in left ear, and tinnitus. No treatment was received for the events hearing loss in left ear and tinnitus. The outcome of the events hearing loss in left ear and tinnitus was not recovered. Since the vaccination, the patient had not been tested for COVID-19. The lot number for the vaccine, BNT162B2, was not provided and will be requested during follow up.

Other Meds: TORSEMIDE; WARFIN; SPIRONOLACTONE

Current Illness:

ID: 1106298
Sex: M
Age:
State: FL

Vax Date: 02/26/2021
Onset Date: 02/27/2021
Rec V Date: 03/16/2021
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Symptoms: Temporary loss of eyesight left eye.; This is a spontaneous report from a contactable consumer (patient). A 68-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number and expiration date were not reported), via an unspecified route of administration, in the left arm on 26Feb2021 10:15 at a single dose (at the age of 68-years-old) for COVID-19 immunisation. Medical history included atrial fibrillation (A-fib) and gout. The patient has no known allergies. Concomitant medication included allopurinol and acetylsalicylic acid (ASPIRIN (E.C.). The patient received the first dose of BNT162B2 (lot number was not reported) in the left arm on 29Jan2021 10:15 (at the age of 68-years-old) for COVID-19 immunisation. No other vaccines were administered within four weeks. No COIVD prior vaccination. On 27Feb2021 at 11:00, the patient experienced temporary loss of eyesight left eye. The patient did not receive treatment for the event. No COVID tested post vaccination. The patient recovered from the event in Feb2021. Information on the lot/batch number has been requested.

Other Meds: ALLOPURINOL; ASPIRIN (E.C.)

Current Illness:

ID: 1106299
Sex: F
Age:
State: PA

Vax Date: 02/25/2021
Onset Date: 02/25/2021
Rec V Date: 03/16/2021
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Symptoms: arm was very sore when she got up it was swollen and red and hurt terribly; arm was very sore when she got up it was swollen and red and hurt terribly; arm was very sore when she got up it was swollen and red and hurt terribly; This is a spontaneous report from a contactable consumer (patient). A 59-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) (at 59 years of age), via an unspecified route of administration in the left arm on 25Feb2021 14:15 (Batch/Lot Number: Unknown) as a single dose for COVID-19 immunisation. Medical history included chronic blood clot in left leg from an unknown date and unknown if ongoing and environmental allergies. The patient's concomitant medications were not reported. The patient did not receive any other vaccine in four weeks prior to covid vaccine. She was not pregnant. The patient had not had covid prior vaccination and she had not been tested post vaccination. It was reported that during the night of 25Feb2021 at 11:00 PM, the patient's arm was very sore when she got up it was swollen and red and hurt terribly. So she went to the ER because she had a chronic blood clot in her left leg; there was no clot in her arm but it was still swollen, red and it hurts. She added that she have very bad environment allergies and queried if she should get the second shot. No treatment received for the events. The outcome of the events was unknown; the events resulted to emergency room visit. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1106301
Sex: F
Age:
State:

Vax Date: 02/26/2021
Onset Date: 02/01/2021
Rec V Date: 03/16/2021
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Symptoms: severe upper abdominal pain/very bad stomach ache; flush through her body; rash/flush through her body; she felt a little weird; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE) on 26Feb2021 at single dose for COVID-19 immunisation. Medical history and concomitant medications were not reported. About 30-35 minutes after receiving the injection, in Feb2021, the patient developed severe upper abdominal pain/very bad stomachache. She also experienced a rash/flush through her body in Feb2021 and she felt like she was going to die. After experiencing that, she felt a little weird for a minute or so. Then the flush/rash happened again but not as bad as the initial flush. The stomachache lasted for 2 hours then it stopped. The patient had recovered from severe upper abdominal pain/very bad stomachache and she felt a little weird in Feb2021, the outcome of the other events was unknown. Information on about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1106302
Sex: F
Age:
State: MI

Vax Date: 01/28/2021
Onset Date: 02/02/2021
Rec V Date: 03/16/2021
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Symptoms: When probed for are the events worsened improved or still persisting consumer stated "Worsened"; Blood Sugar went up; This is a spontaneous report from a contactable consumer (patient). A 69-year-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL9265, expiry date not reported), via an unspecified route of administration on 28Jan2021 at single dose, and second dose (lot number: EN6200, expiry date not reported), via an unspecified route of administration on 19Feb2021 at single dose for COVID-19 immunization. Medical history included blood pressure measurement, hypothyroidism (low thyroid), and diabetes mellitus. Concomitant medications included thyroid (ARMOUR THYROID) for hypothyroidism and liothyronine. The patient's blood sugar went up on 02Feb2021. When probed if the event worsened improved or still persisting, the consumer stated "worsened" on an unspecified date. On an unspecified date, the patient underwent lab tests and procedures which included blood pressure measurement:high and thyroid function test: low. Clinical outcome of blood sugar went up was not recovered while unknown for the other event. Information about lot/batch number has been obtained.

Other Meds: ARMOUR THYROID; LIOTHYRONINE

Current Illness:

ID: 1106303
Sex: F
Age:
State: CT

Vax Date:
Onset Date: 02/20/2021
Rec V Date: 03/16/2021
Hospital: Y

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Symptoms: broken femur; early morning fall (maybe related); lethargy; memory issues (beyond normal for her); low grade fever; This is a spontaneous report from a contactable consumer. An 88-years-old (non-pregnant) female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiration date unknown), via an unspecified route of administration on an unspecified date at a single dose for COVID-19 immunization. Medical history included chronic obstructive pulmonary disease (COPD). Concomitant medications included atorvastatin (ATORVASTATIN), gabapentin (GABAPENTIN), lorazepam (LORAZEPAM), losartan (LOSARTAN), metoprolol succinate (METOPROLOL SUCCINATE), pantoprazole (PANTOPRAZOLE), paroxetine (PAROXETINE), and zolpidem (ZOLPIDEM). The patient had no other vaccines in four weeks. The patient had no COVID prior vaccination. On 20Feb2021 at 12:00, the patient had a low-grade fever for 2 days, followed by lethargy and memory issues (beyond normal for her) on the 3rd day (23Feb2021). Finally, on the 4th day (24Feb2021), by early morning, the patient had a fall (maybe related) and a broken femur. The events resulted in emergency room/department or urgent care, hospitalization as the patient was hospitalized for two days due to the events. Treatment for the events was unknown. The patient underwent lab tests and procedures which included Blood test/viral RNA: Negative on 26Feb2021. The events had not resolved. Information on the batch/lot number has been requested.

Other Meds: ATORVASTATIN; GABAPENTIN; LORAZEPAM; LOSARTAN; METOPROLOL SUCCINATE; PANTOPRAZOLE; PAROXETINE; ZOLPIDEM

Current Illness:

ID: 1106304
Sex: M
Age:
State: NY

Vax Date: 02/05/2021
Onset Date: 02/01/2021
Rec V Date: 03/16/2021
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Symptoms: he has lost also since he got that shot he had lost 8 pounds in like 4 days. He weighs not like a 117-118 pounds; Headache; His arm was hurting; It is the ringing in the ear; felt like a siren was going both of his ears; This is a spontaneous report from a contactable consumer (parent). A 38-year-old male patient (son) received first dose of BNT162B2 on 05Feb2021 at single dose for COVID-19 immunisation. Medical history and concomitant medications were none. When he received the first one he felt headache a little bit and his arm was hurting and all of a sudden he suffers from tinnitus, It is the ringing in the ear. He is about 5' 9 and he has lost also since he got that shot he had lost 8 pounds in like 4 days. He weighs not like a 117-118 pounds. The outcome of the events was unknown. Information on the Lot/batch number has been requested.

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Current Illness:

ID: 1106305
Sex: F
Age:
State: IL

Vax Date: 02/13/2021
Onset Date: 02/22/2021
Rec V Date: 03/16/2021
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Symptoms: So much pain that she could not move her left arm; So much pain that she could not move her left arm (the arm that was injected)/ moved to her right arm; This is a spontaneous report from a contactable consumer (patient). A 78-year-old female patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, lot# EL9266), via an unspecified route of administration on the arm on 13Feb2021 at a SINGLE DOSE for COVID-19 immunization. Medical history and concomitant medications were not reported. She had the shot on the 13Feb2021 and was fine, but reported that a week and 2 days later (22Feb2021) she was in so much pain that she could not move her left arm (the arm that was injected) and 2-3 days later this moved to her right arm. The patient spoke to her healthcare professional regarding this and was prescribed a muscle relaxant. Outcome of the events were unknown.

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Current Illness:

Total 2021 VAERS Injuries: 704,237

Page last modified: 03 October 2021 5:28pm