VAERS 2021 Database www.vaers.hhs.gov

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







Manufacturers

Total Manufacturer

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: 1224430
Sex: M
Age:
State: CO

Vax Date: 03/27/2021
Onset Date: 03/28/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: irritability; tinnitus; body temperature fluctuations with no fever; suicidal ideation; Extreme fatigue; depressed mood; brain fog; This is a spontaneous report from a contactable other hcp (patient). A 30-years-old male patient received bnt162b2 (BNT162B2), via an unspecified route of administration on 27Mar2021 (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation. The patient medical history was not reported. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient's concomitant medications were not reported. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced suicidal ideation, extreme fatigue, depressed mood, brain fog, irritability, tinnitus, body temperature fluctuations with no fever on 28Mar2021. The patient underwent lab tests and procedures which included body temperature: fluctuations with no fever on 28Mar2021. No treatment was received for the events. The reporter considered the events as non-serious. The event outcome was recovering. Since the vaccination, the patient had not been tested for COVID-19. Information on the lot/batch number has been requested.; Sender's Comments: Considering close temporal association, a possible contributory role of bnt162b2 to the reported events cannot be completely excluded. However the clinical course, relevant medical history and concomitant medications are pending for a medically meaningful assessment. 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 RAs, Ethics Committees, and Investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1224431
Sex: F
Age:
State: CT

Vax Date: 03/30/2021
Onset Date: 03/30/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: fatigue; fever; pain at the injection site; lumbar pain; This is a spontaneous report from a contactable consumer (patient). A 53-years-old female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Arm Left on 30Mar2021 10:30 (Batch/Lot Number: EP6955) as single dose for Covid-19 immunisation. Medical history included allergies to Voltaren. Not pregnant at the time of vaccination. Historical Vaccine included first dose of BNT162B2 on 09Mar2021 Administration time: 09:30 AM, Lot number: EL3247, Vaccine location: Left arm. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Did not receive any other medications within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient's concomitant medications were not reported. The patient experienced fatigue, fever, pain at the injection site and lumbar pain on 30Mar2021. Since the vaccination, the patient had not been tested for COVID-19. The event outcome was recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224432
Sex: F
Age:
State: NC

Vax Date: 03/27/2021
Onset Date: 03/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: high fever; body pain; headache; chills; sore throat; lost appetite; feels weak; This is a spontaneous report received from a Pfizer sponsored program Covax US Support. A contactable consumer (patient) reported a female patient of an unspecified age received a first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number and Expiration dates were not reported), via unspecified route of administration on 27Mar2021 as single dose for COVID-19 immunization. The patient had medical history of tested positive for Covid-19 on Dec2020, she was hospitalized and released on 03Jan2021. The concomitant medication was not reported. The patient reported that she woke up at the night of vaccination with high fever, body pain, headache, chills, sore throat and lost appetite. The next day she still feels weak, she still has it but not just like yesterday. The outcome of the events was unknown. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1224433
Sex: M
Age:
State: IL

Vax Date: 03/10/2021
Onset Date: 03/13/2021
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: appendicitis; This is a spontaneous report from a contactable consumer (patient). A 66-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), at the age of 66-year-old via an unspecified route of administration, administered in Arm Right on 10Mar2021 15:15 (Lot Number: EN6199) as single dose for covid-19 immunisation. Medical history included High blood pressure, asthma. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. No COVID prior vaccination. No known allergies. Concomitant medication included lisinopril received within 2 weeks of vaccination. The patient previous received first dose of BNT162B2 (Lot Number: EL9267) in Right arm on 17Feb2021 15:15 as single dose for covid-19 immunisation. The patient experienced appendicitis on 13Mar2021, resulted in Emergency room/department or urgent care. The patient was hospitalized for appendicitis for 2 days. The patient had an appendectomy. The patient underwent lab tests and procedures which included covid-19 (Nasal Swab): negative on 16Mar2021. The outcome was recovering.

Other Meds: LISINOPRIL

Current Illness:

ID: 1224434
Sex: F
Age:
State: MI

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: upset stomach; This is a spontaneous report received from a Pfizer sponsored program. A contactable female consumer reported for her mother (patient) age 86 years that she received the second dose of BNT162B2 (Pfizer-BioNTech COVID-19 Vaccine; Solution for Injection) via an unspecified route of administration as a SINGLE DOSE on unspecified date in 2021 (reported as a week ago) for COVID-19 immunization. Medical history included the first dose of BNT162B2 for COVID-19 immunization. The patient concomitant medications were not reported. Approximately on an unknown date in 2021, the patient, was having an upset stomach and wanted to know if this was caused by the vaccine. The outcome of the event upset stomach was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224435
Sex: F
Age:
State: CO

Vax Date: 02/27/2021
Onset Date: 03/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: I have experienced what seems like an excellerated cataract deterioration; I am also experiencing a high sensitivity to light.; This is a spontaneous report from a contactable nurse (patient). A 70-year-old female patient received second dose bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), via an unspecified route of administration, administered in left arm at age of 70-year-old on 27Feb2021 10:00 (Lot Number: EN6205) as single dose for COVID-19 immunisation. Facility where the most recent COVID-19 vaccine was administered was hospital. The patient medical history was not reported. Patient was not pregnant. Prior to vaccination, the patient was not diagnosed with COVID-19. No allergies to medications, food, or other products. There were no concomitant medications. The patient previously took first dose of bnt162b2 at age of 70-year-old on 06Feb2021 10:30 in left arm for Covid-19 immunization. Patient had experienced what seems like an excellerated cataract deterioration on 01Mar2021. Patient was also experiencing a high sensitivity to light on 01Mar2021. Seriousness Criteria was disability. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The adverse event result in Doctor or other healthcare professional office/clinic visit. No treatment was received for the adverse events. The outcome of events was not recovered. Information on the lot/batch number has been requested.; Sender's Comments: The information available in this report is limited and does not allow a medically meaningful assessment of the case. Based on the information currently available, a causal association between the reported events and bnt162b2 cannot be fully excluded. Case will be reassessed when additional information is available.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 RAs, Ethics Committees, and investigators, as appropriate.

Other Meds:

Current Illness:

ID: 1224436
Sex: M
Age:
State: NE

Vax Date: 03/17/2021
Onset Date: 03/19/2021
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: deep vein thrombosis on Sunday; Extreme fatigue on Friday; This is a spontaneous report received from a contactable consumer. A 72-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EN6208) via unspecified route on left arm single dose for COVID-19 immunization on 17Mar2021, 10:45 AM, at 72-year-old. Medical history was not reported. The patient had not had COVID prior vaccination. Concomitant medications in two weeks included: fluoxetine 20 mg; atorvastatin 10 mg. The patient had not had other vaccine in four weeks. The patient previously took morniflumate (FLOMAX) and had allergy to it. The patient was extreme fatigue on Friday 19Mar2021 and deep vein thrombosis on Sunday 21Mar2021 06:00 PM. I was hospitalized for two days including a veinogram to remove the blood clots from my left leg. I'm now taking rivaroxaban (XARELTO) 15 mg twice a day and were wearing a compression sock for my left leg. Treatment also received as IV heparin. Emergency room/department or urgent care involved and reported as serious due to hospitalization for 2 days. The patient had not had COVID tested post vaccination. Outcome of the events was resolving.

Other Meds: FLUOXETINE; ATORVASTATIN

Current Illness:

ID: 1224438
Sex: F
Age:
State: DE

Vax Date: 02/16/2021
Onset Date: 02/18/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Pharyngeal swelling

Symptoms: Post menopausal bleeding; vaginal bleeding; This is a spontaneous report from a contactable physician (patient) reported for herself. A 57-year-old female patient received 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, LOT number: EL9266, expiration date unknown) via unspecified route of administration at arm right on 16Feb2021 16:15 at age of 57-year-old at single dose for COVID-19 immunisation. Patient was not pregnant at time of vaccination. Medical history included hypertension, allergic to Cipro. Patient previously received 1st dose of BNT162B2 on 21Jan2021 at 02:00 PM (Lot number: EL3246) at single dose for COVID-19 immunisation. Concomitant medications included lisinopril, biotin/ cyanocobalamin/ folic acid (MVI 3), vitamin D3. Patient didn't receive any other vaccines within 4 weeks prior to the COVID vaccine. LMP 7/2018 No significant gynecological history other than pregnancies/childbirth. No prior abnormal vaginal/uterine bleeding. No known history pf uterine fibroids. No h/o bleeding/coagulation disorder. On 18Feb2021, patient experienced vaginal bleeding began with light flow and gradually increased with use of pads and tampons. There was no clots. Menstrual period lasted until 23Feb2021. (This appeared to be similar to menstrual periods in the past except there was no cramping on the first day and in the past would have expected to end on 22Feb2021. No further vaginal/uterine bleed or spotting since 23Feb2021. On 19Feb2021, platelet was 349 (normal range: 150-450). On 16Mar2021, endometrial biopsy was negative. On 16Mar2021, Pap (Smear cervix) was negative. On 16Mar2021, ultrasound showed endometrial thickness within normal range 4 mm, 2 small fibroids 1 cm, 2 cm, normal ovary sizes, small L ovarian cyst. Prior to vaccination, the patient wasn't diagnosed with COVID-19. Since the vaccination, the patient been tested for COVID-19 by COVID-19 PCR (SARS-CoV-2) saliva with unknown results. It was reported that patient experienced Post menopausal bleeding on 18Feb2021 at 12:30 and vaginal bleeding on 18Feb2021 at 12:30. Outcome of events was recovered on 23Feb2021. Events resulted in doctor or other healthcare professional office/clinic visit. There was no treatment for the events.; Sender's Comments: Based on the information provided, reported events are not related to suspect product. Case will be reassessed when additional information is available. The impact of this report on the benefit/risk profile of the Pfizer drug 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: LISINOPRIL; MVI 3; VITAMIN D3

Current Illness:

ID: 1224439
Sex: F
Age:
State: CT

Vax Date: 03/28/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: she felt a tingling sensation on her elbow down to her hand; she experienced numbing of the pinky and ring finger on her left; This is a spontaneous report from a contactable consumer or other non hcp (Patient) via Pfizer Sponsored Program. A female patient of an unspecified age received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number and expiration date not reported) via an unspecified route of administration on 28Mar2021 as single dose for covid-19 immunization. The patient medical history and concomitant medications was not reported. On an unspecified date, the patient experienced numbing of the pinky and ring finger on her left arm where she was injected; in addition, she felt a tingling sensation on her elbow down to her hand. The second dose is scheduled on April 18. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224440
Sex: F
Age:
State:

Vax Date: 03/24/2021
Onset Date: 03/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Diarrhoea, Nasal congestion

Symptoms: She did not get her period she may be PG (she has not tested yet); This is a spontaneous report from a Pfizer sponsored program . A contactable consumer (patient) reported that a female patient of an unspecified age received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration on 24Mar2021 at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient reported, received first covax on 24Mar. She did not get her period she may be PG (she has not tested yet) and is asking if there is any information on pregnancy . The outcome of event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224441
Sex: M
Age:
State: PA

Vax Date: 03/09/2021
Onset Date: 03/27/2021
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Vaccination site erythema, Vaccination site pruritus, Vaccination site swelling

Symptoms: Chest Pain as a Result of Elevated Troponin Levels Caused by Myocarditis; Chest Pain as a Result of Elevated Troponin Levels Caused by Myocarditis; Chest Pain as a Result of Elevated Troponin Levels Caused by Myocarditis; This is a spontaneous report from Pfizer Sponsored Patient Support Program. A contactable consumer (patient) reported for himself that a 43-year-old male patient received his second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number: EN6202), via an unspecified route of administration at the age of 43-year-old at arm left on 09Mar2021 14:00 at single dose for covid-19 immunisation. Medical history included high blood pressure. The patient wasn't allergies to medications, food, or other products. Concomitant medications included metoprolol tartrate and vitamin D NOS. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number: EN6202) at left arm on 15Feb2021 6:00 PM for COVID-19 immunisation. The patient experienced chest pain as a result of elevated troponin levels caused by myocarditis on 27Mar2021 14:00. The events were serious for being hospitalized (duration 3 days). The adverse events result in Emergency room/department or urgent care. Facility where the most recent COVID-19 vaccine was administered in hospital. Prior to vaccination, the patient wasn't diagnosed with COVID-19. Since the vaccination, the patient has been tested for COVID-19. The patient underwent lab tests included nasal swab: negative on 29Mar2021. The patient was received treatment (Heparin, Nitroglycerin and Cardiac Catheterization) for events. The outcome of events was recovering.

Other Meds: METOPROLOL TARTRATE; VITAMIN D NOS

Current Illness:

ID: 1224442
Sex: F
Age:
State: FL

Vax Date: 03/16/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Rash, Urticaria

Symptoms: sore lump on her right arm and it hurts when it is touched; sore lump on her right arm and it hurts when it is touched; This is a spontaneous report from a contactable consumer. An 83-years-old female patient received first dose of bnt162b2 (BNT162B2, Solution for injection), via an unspecified route of administration in right arm on 16Mar2021 at single dose for COVID-19 immunization. The patient medical history included hip problem, back burn injury and hypertensive (a patch for high blood pressure). Concomitant medications included certain medications. She gets epidural shots for three months now. The patient experienced sore lump on her right arm and it hurts when it is touched on an unspecified date in 2021. The outcome of the event was unknown. She is scheduled to get her second dose on 06Apr2021. No follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1224443
Sex: M
Age:
State: AZ

Vax Date: 03/08/2021
Onset Date: 03/12/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Blood pressure decreased, Chest pain, Chills, Confusional state, Decreased appetite

Symptoms: Full blown shingles outbreak 5 days after second shot; This is a spontaneous report received from a contactable consumer (patient himself). A 73-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Left on 08Mar2021 10:00 (Lot Number: EN6205) (at age of 73-year-old) as single dose for COVID-19 immunization. Medical history included Heart stint. There was no allergies to medications, food, or other products. The patient previously took the first dose of BNT162B2 on unknown date (lot number: unknown) for COVID-19 immunization. The patient concomitant drug was not reported. The patient experienced full blown shingles outbreak 5 days after second shot on 12Mar2021 10:00. The event was reported as serious with seriousness criteria disability. The event resulted in Doctor or other healthcare professional office/clinic visit. Therapeutic measures were taken as a result of 'full blown shingles outbreak 5 days after second shot' includes acyclovir, cababpentin, advil, creams. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The event outcome was not recovered.

Other Meds:

Current Illness:

ID: 1224444
Sex: M
Age:
State: NM

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

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: My father felt like he had a cold, gave him the test; Somewhere between 13th to 15th they go the covid virus; Somewhere between 13th to 15th they go the covid virus; This is a spontaneous report from a contactable consumer received via medical information team. A 71-year-old male patient received first dose of bnt162b2 (Formulation: Solution for injection), via an unspecified route of administration on 01Feb2021 as single dose for covid-19 immunisation. The patient medical history was not reported. The patient's concomitant medications were not reported. On an unspecified date in Feb2021, the patient experienced somewhere between 13th to 15th they go the covid virus. On an unspecified date the patient experienced my father felt like he had a cold, gave him the test. Calling on behalf of his parents who received the first dose of the Pfizer covid vaccine on 01Feb2021. Somewhere between 13th to 15th they go the covid virus. My father felt like he had a cold, gave him the test. The patient did not receive any treatment for the events. The outcomes of events the events was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224445
Sex: M
Age:
State: NY

Vax Date: 03/17/2021
Onset Date: 03/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Heart rate decreased, Heart rate increased, Hypertension, Injection site pain, Musculoskeletal chest pain

Symptoms: Pfizer 1st Shot gave me loud Tinnitus and hasn't stopped.; headache; Had fever for a few days; fatigued; arm soreness; he was scared; This is a spontaneous report from a contactable consumer (patient). A 48-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 17Mar2021 11:30 (Batch/Lot Number: EN6204) as SINGLE DOSE for covid-19 immunisation, age of vaccination 48 years old at workplace clinic. Medical history included Heart Disease and Covid-19 from an unknown date. No other vaccines in four weeks. Concomitant medication included losartan taken for an unspecified indication, start and stop date were not reported. The patient experienced loud tinnitus and hasn't stopped. Described as screaming High Pitch Ringing. Patient stated he was praying it will go away. Patient had headache, had fever for a few days, fatigued, and arm soreness on 19Mar2021 20:30 with outcome of not recovered. The patient underwent lab tests and procedures which included sars-cov-2 test (nasal swab): negative on 20Mar2021. Treatment was not received for tinnitus, headache, had fever for a few days, fatigued, and arm soreness. Physician office visit was made for tinnitus, headache, had fever for a few days, fatigued, and arm soreness. The patient stated "This is really scary stuff. Please stop blaming it on Covid". Patient further stated, "Since day 2 of shot which I got on St Patty's Day 17Mar2021. I am on Day 13 of this new hell with no end in sight". He filed a VAERS report and notified his Primary care Dr and ENT. Patient won't get the 2nd shot, as he was scared (Mar2021)." Outcome of the event scared was unknown while not recovered for the other events. The patient considered the tinnitus as serious (very serious and others have experienced this). No follow-up attempts are possible. No further information is expected. Lot number has been obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021366081 Same reporter/drug/AE, different patient;US-PFIZER INC-2021366082 Same reporter/drug/AE, different patient

Other Meds: LOSARTAN

Current Illness:

ID: 1224446
Sex: F
Age:
State: WA

Vax Date: 03/25/2021
Onset Date: 03/30/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Nausea, Pain, Pain in extremity, Paraesthesia oral, Pyrexia

Symptoms: Blood was coming out both nostrils and down throat and could not be stopped without intervention; went to emergency room with gushing bloody nose that would stop. Blood was coming out both nostrils and down throat and could not be stopped without intervention; Bruising also noticed on arm and leg; This is a spontaneous report from a contactable HCP (patient). A 52-years-old female patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Arm Left on 25Mar2021 12:00 (Lot Number: EP7534) as SINGLE DOSE for covid-19 immunisation. Medical history included Allergic to penicillin (body rash). Prior to vaccination, the patient was not diagnosed with COVID-19. The patient was not pregnant at the time of vaccination. Concomitant medication(s) included fexofenadine hydrochloride (ALLEGRA) for Allergy pills and multi-vitamins. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient previously took bnt162b2 dose 1 in arm left on 04Mar2021 (lot number: EN6198) for covid-19 immunization. The patient experienced blood was coming out both nostrils and down throat and could not be stopped without intervention, went to emergency room with gushing bloody nose that would stop, bruising also noticed on arm and leg on 30Mar2021 16:00. Reported as: On Tuesday 30Mar2021 went to emergency room with gushing bloody nose that would stop. Blood was coming out both nostrils and down throat and could not be stopped without intervention. Bruising also noticed on arm and leg. Bleeding resumed after returning home from ER, used Afrin to stop (Afrin up both nostrils). Now stabilize. The adverse event result in Emergency room/department or urgent care. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was recovering. No follow-up attempts are needed. No further information is expected; Sender's Comments: The events "blood was coming out both nostrils and down throat" most likely represent intercurrent medical conditions that are assessed as unrelated to BNT162B2. The case will be reassessed when additional information becomes available. 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.

Other Meds: ALLEGRA

Current Illness:

ID: 1224447
Sex: F
Age:
State: CA

Vax Date: 03/26/2021
Onset Date: 03/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: Shaking chills; vomiting; fever; extreme achiness; This is a spontaneous report received from a contactable consumer reporting for herself. A 69year old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) via an unspecified route of administration on 26Mar2021 as SINGLE DOSE for COVID-19 immunization. The patient did not have underlying conditions and rarely get ill. The patient's concomitant medications were not reported. On Mar2021 (10 hours after vaccination), the patient experienced shaking chills for about 3 hours, vomiting, fever, extreme achiness etc. which lasted about 22 hours. The outcome of the events was unknown. No follow-up attempts are needed. Information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224448
Sex: F
Age:
State:

Vax Date: 03/04/2021
Onset Date: 03/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: 1st shot, she experienced nausea and pain; 1st shot, she experienced nausea and pain; This is a spontaneous report from a contactable consumer via Pfizer-sponsored program. An 85-year-old female patient received first dose of bnt162b2, Solution for injection (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 04Mar2021 (Batch/Lot number was not reported) as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. On an unspecified date in Mar2021, the patient experienced nausea and pain. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224449
Sex: U
Age:
State: MO

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: random pain in the lymph nodes in neck.; Very Runny Nose for a week.; This is a spontaneous report received from a Pfizer sponsored program from a contactable consumer. A patient of unspecified age and gender received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) single dose for covid-19 immunization. Medical history included Sjogren's from an unknown date and inadequate mucus from an unknown date. The patient's concomitant medications were not reported. The patient experienced random pain in the lymph nodes in neck and very runny nose for a week on an unspecified date. The outcome of random pain in the lymph nodes in neck and very runny nose for a week was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224450
Sex: F
Age:
State: NC

Vax Date: 03/04/2021
Onset Date: 03/01/2021
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: a-fib/ heart condition; This is a spontaneous report from a Pfizer sponsored program. A contactable consumer (patient) reported that a 79-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number and expiration date unknown) via an unspecified route of administration on 04Mar2021 (unknown age at time of vaccination), at single dose, for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient stated she got her first shot on 04Mar2021 and is supposed to get her second shot. Since her first shot, she ended up in the ICU for 2 days and now has a-fib (in Mar2021) and they don't know what caused it. She was put on blood thinners, two different ones, and was put on a heart monitor. She had to be hospitalized due to heart condition. Clarified heart condition was not preexisting. She asked if she can get the second dose of the vaccine with the heart monitor. She asked if she can get the vaccine if she is on a blood thinner. Therapeutic measures were taken as a result of the event and included blood thinners and heart monitor. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224451
Sex: F
Age:
State: FL

Vax Date: 03/19/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pruritus, Injection site swelling, Lymph node pain, Lymphadenopathy

Symptoms: lightheaded for 2-3 weeks; sore under armpits (lymph nodes); The pain at times is bad; This is a spontaneous report from a contactable consumer. This 66-year-old female consumer reported that she received 2nd dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; lot EW6200) on 19Mar2021 at left arm for COVID-19 immunisation. Medical history included high cholesterol and allergies: Sulfar, penicillin. Historical vaccine included 1st dose of BNT162B2 (lot EL9262) on 26Feb2021 at left arm for COVID-19 immunisation with adverse event lightheaded and dizzy. Concomitant drugs included ibuprofen, simvistatin, paracetamol (TYLENOL) and ascorbic acid, ergocalciferol, nicotinamide, retinol, riboflavin, thiamine hydrochloride (VITAMINS). The patient was lightheaded for 2-3 weeks, sore under armpits (lymph nodes) which was still effecting her 2 weeks after the second dose was administered. Event resulted in Doctor or other healthcare professional office/clinic visit and no treatment was received except paracetamol or Ibuprofen for pain. She was concerned about this because it was affecting her life and job. The pain at times was bad (She used heating pad to relieve pain). The patient reported lightheaded, dizzy and pain underneath the arm pits, she guessed in the lymph nodes. She was curious as to how long those lymph node pains were going to be around because sometimes it's so painful that she thought she was having a heart attack but people say - No, that's lymph node which is going into your breast. She was concerned about how long this was going to be happening to her or what she was supposed to be doing. Covid test with nasal swab on 17Mar2021 was negative. The patient had complete blood count, urine analysis, Lipid Panel for Cholesterol. The outcome of the events was not resolved.

Other Meds: IBUPROFEN; SIMVASTATIN; TYLENOL; VITAMINS [ASCORBIC ACID;ERGOCALCIFEROL;NICOTINAMIDE;RETINOL;RIBOFLAVIN;THIAMINE HYDROCHLORIDE]

Current Illness:

ID: 1224452
Sex: U
Age:
State: MO

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: With second shot, I had Lots of Saliva; This is a spontaneous report received from a contactable consumer (patient) via Pfizer sponsored program . A patient of an unspecified age and gender received second dose of BNT162B2 (Formulation: Solution for injection) via an unspecified route of administration on an unspecified date at single dose for Covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient previously took first dose of BNT162B2 on an unspecified date at single dose for Covid-19 immunization. It was reported that, "had Sjogren's, an autoimmune disease. Body had inadequate mucus. After first COVID shot, the patient had random pain in the lymph nodes in neck. Also had a very runny nose for a week. With second shot, had lots of saliva. Understood mRNA was being used in clinical trials or to be used in clinical trials with multiple sclerosis and strongly suggested, Pfizer look into mRNA and Sjogren's". Outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224453
Sex: M
Age:
State:

Vax Date:
Onset Date: 03/31/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: tested positive for covid-19 despite receiving two doses of vaccine; tested positive for covid-19 despite receiving two doses of vaccine; This is a spontaneous report from a non-contactable consumer (patient). A 50-years-old male patient received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: unknown), via an unspecified route of administration on an unspecified date as SINGLE DOSE (50 years at the time of vaccination) for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient had no known allergies. The patient did not have COVID prior vaccination. On 31Mar2021, the patient was tested positive for covid-19 despite receiving two doses of vaccine. The patient did not receive any treatment for the events. The patient was recovering from the event of COVID-19 while the outcome of event drug ineffective was unknown. No follow-up attempts are possible. information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224454
Sex: F
Age:
State: MI

Vax Date: 03/30/2021
Onset Date: 03/30/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site pain, Pain

Symptoms: I blacked out completely; Felt very dizzy; fallen on the dresser; hit myself on my stomach and leg; hit myself on my stomach and leg; Was completed disoriented; Headache; Sore arm; Body ache; wound on my stomach; This is a spontaneous report from a contactable consumer (patient). A 30-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration in Arm Left on 30Mar2021 19:45 as single dose for covid-19 immunization. The patient medical history was not reported. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient was not pregnant. Concomitant medications were unspecified received within 2 weeks of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. After taking the vaccine at 19:45, the patient drove back home and had minor symptoms when she went to bed (headache, sore arm, body ache) on 30Mar2021. She woke up around 3:45 am on 31Mar2021 to use the restroom and felt very dizzy. While walking back to bed, she blacked out completely, fallen on the dresser and hit herself on her stomach and leg. She was feeling extremely dizzy at this point, was completed disoriented and couldn't process what was happening around me. Her husband walked her back to bed and put her to sleep. Treatment was reported as First aid for the wound on her stomach. Since the vaccination, the patient had not been tested for COVID-19. The report was non-serious. The outcome of the events was recovering. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224455
Sex: F
Age:
State:

Vax Date: 03/27/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: seems more confused and fatigued than usual afterward; seems more confused and fatigued than usual afterward; This is a spontaneous report received from a Pfizer-sponsored program. A non-contactable consumer reported that a female patient of an unspecified age received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: unknown), via an unspecified route of administration on 27Mar2021 at a single dose for covid-19 immunization. Patient had medical history of Alzheimer's which was prior to receiving first dose of vaccine. The patient's concomitant medications were not reported. On an unspecified date, after receiving the first dose, the patient seems more confused and fatigued than usual afterward. The outcome of events was unknown. No follow up attempts are possible; information about lot number/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224456
Sex: F
Age:
State:

Vax Date: 02/05/2021
Onset Date: 02/06/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: Fever- over 102; Body aches; Chills; Nausea; This is a spontaneous report from a contactable consumer (patient). This 46-year-old female patient received the 1st dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: E13247), via an unspecified route of administration in the right arm on 05Feb2021 03:30 PM at single dose for COVID-19 immunization. Medical history and concomitant medications were unknown. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient experienced fever- over 102, body aches, chills, nausea on 06Feb2021 at 02:00 PM. The patient was not pregnant at the time of vaccination. No treatment received for the adverse event. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19. The patient had covid test post vaccination via nasal swab with negative result. Outcome of the events was recovered. No Follow-up attempts are needed. No further information is expected.

Other Meds:

Current Illness:

ID: 1224457
Sex: F
Age:
State: CO

Vax Date: 03/11/2021
Onset Date: 03/31/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: tested positive for covid 19 infection; tested positive for covid 19 infection; This is a spontaneous report from a contactable pharmacist via a 43-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 11Mar2021 at single dose for COVID-19 immunisation at the age of 43-year-old. Lot number was EN6208. Medical history and concomitant medications were unknown. On 31Mar2021, the patient resulted positive to Covid-19 test. The outcome of the event was unknown.; Sender's Comments: The contributory role of the suspect product BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE to reported events cannot be excluded. This case will be reassessed if follow-up information is received.

Other Meds:

Current Illness:

ID: 1224458
Sex: M
Age:
State: FL

Vax Date: 03/12/2021
Onset Date: 03/20/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: metallic taste in mouth beginning approximately 10 days after vaccine and still persisting 10 days later; This is a spontaneous report from a contactable consumer. A 61-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in left arm on 12Mar2021 12:45 as single dose for covid-19 immunisation. The patient medical history was not reported. No covid prior vaccination, no covid tested post vaccination. No allergies. Concomitant medication(s) included Diltiazem ER 240mg, Rosuvastatin 10mg, Fortest 50. The patient experienced metallic taste in mouth beginning approximately 10 days after vaccine and still persisting 10 days later on 20Mar2021 with outcome of not recovered with no treatment. No follow-up attempts are possible; information about lot/batch number cannot be obtained

Other Meds: DILTIAZEM; ROSUVASTATIN; FORTESTA

Current Illness:

ID: 1224459
Sex: F
Age:
State: IA

Vax Date: 02/13/2021
Onset Date: 02/13/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: faint; tired; chills; mild diarrhea; This is a spontaneous report from a contactable consumer (patient). This 72-year-old female patient received bnt162b2 dose 1 intramuscular in right arm on 13Feb2021 16:00 PM (Lot number unknown) at single dose for COVID-19 immunization. The patient had known allergies to penicillin and shellfish. Other medical history was not provided. The patient's concomitant medications included atorvastatin, vitamin, fish oil, probiotic. 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. The patient became faint, tired and had chills which caused mild diarrhea from 13Feb2021 05:00 PM. The patient did not receive treatment for the event. Since the vaccination, the patient has not been tested for COVID-19. The patient received the bnt162b2 dose 2 intramuscular in Right arm on 06Mar2021 01:15 AM (Lot number unknown) at single dose for COVID-19 immunization. The outcome of the event events was recovered. Information on the lot/batch number has been requested.

Other Meds: ATORVASTATIN; FISH OIL

Current Illness:

ID: 1224460
Sex: M
Age:
State:

Vax Date: 02/25/2021
Onset Date: 03/01/2021
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: 2 weeks after taking the vaccine and had developed a Peritonitis which is fungal in nature; This is a spontaneous report from a contactable consumer who reported for his father that an 85-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 25Feb2021 as single dose for covid-19 immunisation. Medical history included peritoneal dialysis. The patient's concomitant medications were not reported. Patient's son asking in behalf of his father seeking information if these is any reported data on patient undergoing peritoneal dialysis experiencing peritonitis (fungal in nature) as a side effect after taking the PFIZER BIONTECH COVID19 vaccine. Also, he was asking if there were any reported serious adverse events as well with other patients with co-morbidities after taking the Pfizer Biontech Covid19 Vaccine. Patient had the first dose of the vaccine 25Feb2021, he is a peritoneal dialysis patient and has been hospitalized since 10Mar2021, 2 weeks after taking the vaccine and had developed a Peritonitis which is fungal in nature (Mar2021). He also mentioned that he and his family has been sanitary and careful in caring for their father given the underlying condition. He also mentioned that 25% of the people he knew with underlying condition such as heart disease, Hashimoto's, Raynaud syndrome and Chron's disease had experience side effects after taking the vaccine. Outcome of the event was unknown. Information about lot/batch has been requested.

Other Meds:

Current Illness:

ID: 1224461
Sex: M
Age:
State: MA

Vax Date: 03/24/2021
Onset Date: 03/24/2021
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site pain

Symptoms: This is a spontaneous report from a contactable consumer. This consumer reported that her 56 years-old male son (patient) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at single dose for COVID-19 immunisation on 24Mar2021. Relevant history and concomitant drugs were unknown. The reporter stated that her 56 year old son received his first dose of the Pfizer BioNTech COVID-19 vaccine a day earlier than she received hers (which was on 25Mar2021) and while waiting after getting his vaccination, her son became "very, very dizzy." He told the nurse working at the vaccination site that the dizziness was getting worse and "getting very bad." He was asked how his breathing was and he told the nurse it was okay, but an ambulance was called for him anyways and he was sent to the hospital. Her son reported feeling better when he laid down but still reported feeling dizzy. At the hospital, her son was told that all the test came back okay. When her son got up to use the restroom with the assistance of the doctor, the doctor told him that he was dehydrated and gave him IV fluids. Caller stated that her son reported feeling "a lot better" after the IV fluids but "couldn't hardly walk" and had to have someone else drive him. Her son reported feeling "alright" the next day. Caller stated that she was reading in the information pamphlet on the Pfizer vaccine that a severe reaction could include dizziness. Caller was worried about her son getting his second dose and think she should speak with his physician before receiving his next dose, and would like to know if this was okay. She was concerned because she states that she had heard that people have gotten sick from the second dose of the vaccine. Outcome of the events was resolving. Information about the Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224462
Sex: F
Age:
State: CA

Vax Date: 03/31/2021
Onset Date: 04/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: Swollen lymph node above left collar bone; This is a spontaneous report from a non-contactable consumer. A 27-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in left arm on 31Mar2021 16:45 (Batch/Lot Number: ER8734) as single dose for covid-19 immunisation. Medical history were none. No pregnant. No 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. No Allergies to medications, food, or other products. Historical vaccination included BNT162B2 on 10Mar2021 08:45, in left arm, dose 1, lot number:EN6206 for covid-19 immunisation. The patient's concomitant medications were not reported. The patient experienced swollen lymph node above left collar bone on 01apr202110:00 with outcome of unknown. Appeared approximately 17 hours after the second Pfizer shot. I had not had any reactions after the first Pfizer shot. No treatment. Follow-up attempts have been completed and no further information is expected.

Other Meds:

Current Illness:

ID: 1224463
Sex: F
Age:
State: OH

Vax Date: 03/24/2021
Onset Date: 03/24/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Chills, Dizziness, Nausea, Pain, Tachycardia

Symptoms: Very red hands; chemical taste in mouth within 5 minutes of shot; Burning tongue and lower front gums within 10 minutes of shot; Burning tongue and lower front gums within 10 minutes of shot; Throat started to burn and swell within 20 minutes of shot; Throat started to burn and swell within 20 minutes of shot; Blood Pressure shot up to 190 over 90 and don't have high blood pressure; Heart rate increased from resting of 65 to 80's and 90's; This is a spontaneous report from a contactable consumer. A 71-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in right arm on 24Mar2021 15:15 (Batch/Lot Number: ER2613) as single dose for covid-19 immunisation in hospital. Medical history included asthma, allergies, intolerance to some narcotics and Opioids. Not pregnant at the time of vaccination. No patient 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. Historical vaccination included BNT162B2 on 3Mar2021 02:45 PM, lot number:EN6205,in right arm, dose 1 for covid-19 immunisation. Concomitant medication(s) included Cortisone shot left shoulder, Rhinocort, Flovent. The patient experienced very red hands and chemical taste in mouth within 5 minutes of shot, burning tongue and lower front gums within 10 minutes of shot, throat started to burn and swell within 20 minutes of shot, blood pressure shot up to 190 over 90 and don't have high blood pressure, heart rate increased from resting of 65 to 80's and 90's on 24Mar2021 15:15 with outcome of not recovered. Therapeutic measures were taken as 3 tablets of predniSONE 20 mg, Allerest. Events are non serious. Follow-up attempts have been completed and no further information is expected

Other Meds: CORTISONE; RHINOCORT [BUDESONIDE]; FLOVENT

Current Illness:

ID: 1224464
Sex: F
Age:
State: IL

Vax Date: 03/26/2021
Onset Date: 03/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Tremor

Symptoms: received her first dose last Friday and 45 mins after the caller said that her face is swollen and she was having itchiness in her whole; received her first dose last Friday and 45 mins after the caller said that her face is swollen and she was having itchiness in her whole body; pain at the back of her neck; her legs started to hurt on the side; breathing issues; This spontaneous report was received from a Pfizer-sponsored program. A Contactable consumer (patient) reported for herself. A female patient of an unspecified age received first dose of BNT162B2 (COVID-19 Vaccine) via an unspecified route of administration (Batch/lot number: unknown) as a single dose on 26Mar2021 Friday, for COVID-19 immunization. Medical history and concomitant medications were not reported. On the same day, 45 minutes later, she felt that her face was swollen and she was having itchiness in her whole body. On an unspecified date in Mar2021, her legs started to hurt on the side, had pain at the back of her neck and she also experienced breathing issues. She took Benadryl. Action taken with the suspect was not reported. The outcome of the events of face swollen and itchiness in whole body, legs started to hurt on the side, had pain at the back of her neck and breathing issues was not reported.

Other Meds:

Current Illness:

ID: 1224465
Sex: M
Age:
State: MA

Vax Date: 03/23/2021
Onset Date: 03/28/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Erythema, Pruritus

Symptoms: Covid 19 positive on 28Mar2021; This is a spontaneous report received from a Pfizer- sponsored program Covax US Support. A male patient of an unspecified age received first dose of bnt162b2 (BNT162B2, formulation: Solution for injection, Lot number: unknown), via an unspecified route of administration on 23Mar2021 as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient was tested positive for covid 19 on 28Mar2021. The second dose is scheduled on 13Apr2021. The outcome of the event was unknown. Information about lot/batch number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021360084

Other Meds:

Current Illness:

ID: 1224466
Sex: M
Age:
State: NC

Vax Date: 03/19/2021
Onset Date: 03/19/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site induration, Injection site pruritus, Injection site swelling, Myalgia

Symptoms: fever; chills; muscle aches; nausea; fatigue; cough; very sick; This is a spontaneous report from a contactable consumer. A 58-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in left arm on 19Mar2021 04:00 as single dose for covid-19 immunisation. Within 30 minutes of receiving the vaccine, on 19Mar2021 16:30, patient got very sick: fever, chills, muscle aches, nausea, fatigue, cough. The fever broke early the next morning but the other symptoms remained for 2 more days. At that point, he continued having fatigue, cough, nausea and chills for a further 5-6 days. At that point, and continuing now, he still have low level nausea, fatigue and a cough. It's very slowly getting better but it has take 2 weeks to not feel completely sick. The patient underwent lab tests and procedures which included viral test (Nasal Swab, Aegis PCR): negative on 01Mar2021. No treatment. Outcome was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1224467
Sex: M
Age:
State:

Vax Date: 01/14/2021
Onset Date: 02/02/2021
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: sick and went to the hospital and had Covid pneumonia; sick and went to the hospital and had Covid pneumonia; This is a spontaneous report from a non-contactable consumer (patient). A male patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration on 14Jan2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The patient stated he took his 1st Pfizer vaccine dose on 14Jan2021 and then on 02Feb2021 he was sick and went to the hospital and had Covid pneumonia. He was in hospital until 09Feb2021, when he was discharged they said he should isolate for 7 days (until 16Feb2021). The patient stated that (Pharmacy name) came on 24Feb2021 to give the 2nd vaccine dose and he was told by (Pharmacy name) that he had to wait 30 days to get his next shot. The patient asked when can he safely get the 2nd dose. The outcome of the events was unknown. No follow-up attempts are possible, information about lot/batch number cannot be obtained.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021364193 similar report from same reporter

Other Meds:

Current Illness:

ID: 1224468
Sex: M
Age:
State: TN

Vax Date: 03/15/2021
Onset Date: 03/15/2021
Rec V Date: 04/18/2021
Hospital: Y

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: multi focal pneumonia; atrial fibrillation/the second worst feeling he has ever had since he had his first heart surgery; arm started hurting real bad/a severe pain that radiated down to elbow, arm, chest; This is a spontaneous report from a contactable consumer (patient). A 63-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 15Mar2021(Lot Number: EN6204; Expiration Date: 30Jun2021) as single dose for covid-19 immunisation. Medical history included acute diabetes, acute thyroid disease, covid like in 2021 (10 weeks before), 3 heart surgeries with 12 stents, ongoing chronic obstructive pulmonary disease (COPD)slight case diagnosed in 2016-2017, bad thyroid from 2006 and ongoing and told he had full blown Hashimotos in 2017, bad diabetic from 2015 and ongoing and went into diabetic type coma on 18Dec2015 (sugar when got him out of the parking lot cause he had to drive there was 738 or 768 put him in ICU from 18Dec2015-25Dec2015. Had to give him shots like every 2 hours. Started giving him insulin there but insurance wouldn't approve it so kept him on Metformin. Like 5th or 6th day got it under control), bad heart from 2007 and ongoing (In 2017 he had a heart attack they call 'widowmaker', he was told he hemochromatosis like his brother and sister. Caller stated they got it from his parents, but the doctors can't find it now. He had 3 different heart surgeries and has 12 stents in him. 9 weeks before (2021), he went to the hospital because of his heart, got a real bad heart, been put on a heart transplant list, they told him his blood tries to flow backwards and all of it's going over to the right chamber; after 2 hours after he had been admitted to the hospital they told him he had had a heart attack, level 3-they knew from blood tests they'd done. About 1 hour later said test was positive for COVID. He had no symptoms. While in hospital they gave him Zinc, Vitamin D3, Vitamin B1 and that was it. They kept him 5 days at the hospital. Also reported that went to the hospital for triple bypass heart surgery when he got in said somethings wrong, watch everything on the monitors wouldn't tell him nothing; said your widow maker is completely blocked up 99% had to go in and unblock that up so they can't do any kind of bypass on him again. The only thing they can do was heart transplant or heart graft where they take part of the left chamber and he din't have but like 18% of that left, take it come over whatever they're talking about, he doesn't know it's a heart graft whatever they're talking about there), 2 hernia operations, hemochromatosis (little sister and older brother has hemochromatosis-patient got hemochromatosis (too much iron in the blood) from 1 gene from his mother and 1 gene from his father. Brother doesn't have it anymore; but patient's and his sisters mutated); ongoing blood pressure abnormal; anxiety; ongoing wheezing; ongoing chronic Atrial fibrillation. Concomitant medications included aspirin (ASPIRIN [ACETYLSALICYLIC ACID]) taken to help blood to be thin from 2007 and ongoing; levothyroxine taken for Bad thyroid from 2006 and ongoing; metoprolol succinate taken for blood pressure from 2015 and ongoing; clonazepam taken for anxiety from 2012 to an unspecified stop date; fluticasone propionate taken for sinuses from 2015 and ongoing; insulin glargine (LANTUS) taken for diabetes from 2019 and ongoing; insulin aspart (NOVOLOG) taken for diabetes from 2019 and ongoing; salbutamol (ALBUTEROL HFA) taken for wheezing from 2018 and ongoing; budesonide, formoterol fumarate (SYMBICORT) taken for COPD from 2018 and ongoing; amiodarone (AMIODARONE) taken for atrial fibrillation from 22Mar2021 and ongoing; amoxicillin, clavulanate potassium (AUGMENTIN) taken for an unspecified indication from 22Mar2021 to 29Mar2021; apixaban taken for prevent blood clots and chronic Atrial fibrillation from 22Mar2021 and ongoing. The patient had pneumonia shot and flu shot took that in Sep2020. The was no vaccinations within 4 weeks prior to the BNT162B2.The patient previously received Xanax for anxiety from unknown date to 2012; received Humalog , Glipizide and Metformin for Diabetes. The patient got his first Pfizer COVID-19 Vaccine shot on Monday 15Mar2021 at sometime between 15:30-16:00. Not even an hour after he got the Pfizer COVID-19 Vaccine shot his arm started hurting real bad, felt like a hot ice pick was in his arm-described as it started locally just in one spot, then started getting worse going down to his elbow. About 30-45 minutes after got out of there, he was sick, didn't know what was wrong with him. Also reported as by 16:30 he felt bad and pulled up to a friends house. He would say it was an allergic reaction; starting in his arm, a severe pain that radiated down to elbow, arm, chest, it was hard to breathe since 18Mar2021. He went to a friends house after getting the shot, and by the time he got to the friend's house, he felt sick and laid down for about two hours and just kept feeling worse and worse. After that he went home and went to bed. He stayed in bed Tuesday, 16Mar2021, Wednesday, 17Mar2021 and was able to drag himself out of bed to at least go to the bathroom on Thursday morning, 18Mar2021. When he got out of bed, he couldn't breathe. When he got up Thursday morning he couldn't even move his whole left side, had to grab nightstand and pull himself up to stand up out of the bed; stumbled to the bathroom about 3 feet away.He made his way to the phone and called his sister to tell her to call an ambulance because he couldn't breathe. When he got to the emergency room he was told he was in atrial fibrillation. He stayed in the hospital with primary diagnosis as multifocal pneumonia with atrial fibrillation. Feeling like heart beating out of his chest, machine going off every 2-3 minutes. It took about 9-10 hours to get the atrial fibrillation under control. He stayed in Hospital for 4 days-admitted 18Mar2021-discharged 22Mar2021. He spoke to his heart doctor who said it was hard to breathe due to the Atrial fibrillation and all his doctors say they did not know whether it was a reaction to the covid vaccine.He heard the doctors talking and they were saying they didn't think he was going to make it. His heart rate was going between 80 and 200. He had 3 different IV's going in each arm shooting different heart medications in him and the doctor explained that the medications didn't mix well, could not go in the same IV at the same time. The patient shared that this was the second worst feeling he has ever had since he had his first heart surgery. He meant they thought he was dead or dying he lost feeling of everything. His arm felt better, but every now and again felt like a little knot or something was in there. He was breathing better, they gave him inhalers, albuterol. He thought that his heart doctor was going to start him on oxygen. He went to his Cardiologist on 01Mar2021 on Monday, 2 weeks before getting his first Pfizer COVID-19 Vaccine: cardiologist told him his triglycerides raised up about 15 was about 268. All his Cardiologist did was change his blood pressure medicine. Went to his Endocrinologist on 08Mar2021 Monday, 1 week before he took the Pfizer COVID-19 Vaccine: Endocrinologist raised his Lantus SoloStar U-100 insulin 100 units/mL (3mL) from 60 units nightly to 64 units nightly then. All his other blood tests were good, they just said keep doing what you're doing.The outcome of all the events was resolving. Follow-up attempts are completed. No further information is expected.

Other Meds: ASPIRIN [ACETYLSALICYLIC ACID]; LEVOTHYROXINE; METOPROLOL SUCCINATE; CLONAZEPAM; FLUTICASONE PROPIONATE; LANTUS; NOVOLOG; ALBUTEROL HFA; SYMBICORT; AMIODARONE; AUGMENTIN [AMOXICILLIN;CLAVULANATE POTASSIUM]; APIXABAN

Current Illness: Blood pressure abnormal; Chronic atrial fibrillation; COPD (slight case diagnosed in 2016-2017); Diabetic (Went into diabetic type coma 18Dec2015); Hashimoto's thyroiditis (Told he had full blown Hashimotos in 2017.); Heart disorder; Thyroid disorder (full blown Hashimotos in 2017.); Wheezing

ID: 1224469
Sex: F
Age:
State: CA

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site erythema, Injection site pain, Injection site swelling

Symptoms: small reaction; This is a spontaneous report from a contactable HCP . This HCP reported for a 67-years-old female patient that she received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection) via an unspecified route of administration on an unspecified date at single dose for covid-19 immunisation. Patient's medical history included age related osteoporosis. Type of historical vaccine was reported as vaccination adverse reaction (unspecified). Concomitant medications included abaloparatide (TYMLOS) via a subcutaneous route from 10Aug2019 to ongoing at 80 mcg 1x/day for Age related osteoporosis without therapy. It was reported that the patient took the covid vaccine and had small reaction. Case description: This potential case reported by pharmacy from a consumer is considered invalid with the initial information provided. the case report is missing one or more of the following ICSR minimum elements as defined by the regulations: Adverse event. The outcome of event was unknown. Information on the lot/batch number has been requested.

Other Meds: TYMLOS

Current Illness:

ID: 1224471
Sex: F
Age:
State:

Vax Date: 02/24/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Chills, Feeling cold, Feeling hot, Myalgia, Pain

Symptoms: Does this mean the first dose doesn't work; had an allergic reaction; This is a spontaneous report from a contactable consumer (patient) reported for herself. A female of unspecified age received the first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: UNKNOWN) via an unspecified route of administration on 24Feb2021 as a SINGLE DOSE for COVID-19 immunization. Medical history and concomitant medication were not reported. On 24Feb2021 got first dose and had an allergic reaction to vaccine. The patient enquired about getting the second dose and does that mean vaccine does not work. The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224472
Sex: F
Age:
State: UT

Vax Date: 03/31/2021
Onset Date: 04/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Pain in extremity

Symptoms: Mild Sore throat; This is a spontaneous report from a contactable consumer. A 60-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in left arm on 31Mar2021 10:30 (Batch/Lot Number: EN6207) as single dose for covid-19 immunisation. The patient medical history was not reported. No pregnant. 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 or been tested for COVID-19. Concomitant medication(s) included duloxetine hydrochloride (CYMBALTA); montelukast sodium (SINGULAIR); cetirizine hydrochloride (ZYRTEC ALLERGY); paracetamol (TYLENOL); ibuprofen. The patient previously took amoxicillin and experienced hypersensitivity, septra and experienced hypersensitivity. The patient experienced mild sore throat on 01Apr2021 04:00 with outcome of unknown. No treatment. No follow-up attempts are needed. No further information is expected.

Other Meds: CYMBALTA; SINGULAIR; ZYRTEC ALLERGY; TYLENOL; IBUPROFEN

Current Illness:

ID: 1224473
Sex: F
Age:
State: NY

Vax Date: 03/26/2021
Onset Date: 03/29/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Abnormal behaviour, Adverse reaction, Anger, Asthma

Symptoms: Caller got her first dose of the vaccine on 26MAR2021/Caller tested positive on 29MAR2021; This is a spontaneous report from a contactable consumer or other non hcp (patinet). A 59-years-old female patient received bnt162b2 (BNT162B2), dose 1 via an unspecified route of administration, administered in Arm Left on 26Mar2021 12:15 (Batch/Lot Number: ER8733; Expiration Date: 31Jul2021) as SINGLE DOSE for covid-19 immunisation. Medical history included neck surgery from 2007 to an unknown date, neck surgery from 2010 to an unknown date, migraine, cluster headache, rash on his upper back, feels a little bit itchy on his upper back on 16Mar2021. The patient's concomitant medications were not reported. The patient experienced caller got her first dose of the vaccine on 26Mar2021/caller tested positive on 29Mar2021, she had no symptoms but did not feel 100%, she's wondering if it's dangerous to get vaccinated while having covid, caller believes she might have had covid while she got the vaccine. She's been doing a lot of gardening and working like a maniac" yet no coughing or sneezing. She would like to know if she would notify somebody or if it is safe for her to take the 2nd dose. She also mentioned that she didn't have any symptoms and she didn't know what she was exposed to. Caller stated there were no medical conditions for herself that she feels is related to the reported events but states she is on disability and had two neck surgeries and one was in 2007 and the other was in 2010, stating she had chronic migraines and cluster headaches that she sees a neurologist for and was diagnosed around 2010. Also stated that she had blood drawn the day before on 25Mar2021 just to test her cholesterol and for her thyroid as a routine thing. She did not have results for that testing yet. The HCP only tested the cholesterol, thyroid and stuff so she could refill medications for that. No vaccines administered on same date of the pfizer suspect. The patient underwent lab tests and procedures which included blood cholesterol and thyroid function test on 25Mar2021 whereas sars-cov-2 test was positive on 29Mar2021. The outcome of events was unknown. Follow-up information requested.

Other Meds:

Current Illness:

ID: 1224474
Sex: M
Age:
State: MI

Vax Date: 03/24/2021
Onset Date: 03/27/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Consciousness fluctuating, Crying, Dry skin, Epistaxis, Headache

Symptoms: headache; chills; joint pain; body ache; This is a spontaneous report received from Pfizer-sponsored program. A male contactable consumer (patient) reported for himself that, a male patient of an unspecified age received bnt162b2 (Pfizer-Biontech Covid-19 Vaccine, Solution for injection), dose 1 intramuscular on 24Mar2021 (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient called to report that on the 27Mar2021 he experienced headache, chills, body ache and joint pain three days after he received his 1st dose on 24Mar2021, his 2nd dose schedule was on 17Apr2021. The patient experienced headache, chills, joint pain, and body ache on 27Mar2021. 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: 1224475
Sex: U
Age:
State:

Vax Date: 03/09/2021
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: I have Covid; I have Covid; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received bnt162b2 ((PFIZER-BIONTECH COVID-19 MRNA VACCINE), dose 1, via an unspecified route of administration on 09Mar2021 (Batch/Lot Number: EN6204) as a SINGLE DOSE for COVID-19 immunisation. The patient's medical and concomitant medications were not reported. The patient experienced "I have covid" on an unspecified date prior to the second dose of bnt162b2 (next dose was due 30Mar2021). The clinical outcome of the event drug ineffective and COVID-19 was unknown.

Other Meds:

Current Illness:

ID: 1224476
Sex: M
Age:
State: MI

Vax Date: 03/27/2021
Onset Date: 04/01/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Vomiting

Symptoms: Came down with Bell's palsy symptoms 5 days after injection on the Right side of my face.; This is a spontaneous report from a contactable consumer reported for himself. A 52-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in Arm Right on 27Mar2021 (Lot Number: ER8732) as single dose for covid-19 immunisation. The patient previously took the first dose bnt162b2 on 06Mar2021 for covid-19 immunization. The patient medical history included allergies to penicillin. The patient's concomitant medications were not reported. The patient came down with bell's palsy symptoms 5 days after injection on the right side of face on 01Apr2021 06:00. Facial paralysis resulted in emergency room visit. Therapeutic measures were taken as a result of facial paralysis included Steroid and Viral scripts. The outcome of event was unknown. No other vaccine in four weeks; No covid prior vaccination; No covid tested post vaccination.

Other Meds:

Current Illness:

ID: 1224477
Sex: F
Age:
State: MN

Vax Date:
Onset Date:
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: Flared up Multiple sclerosis; flared up optic Neuritis; numbness; pressure at the base of her neck; head pressure; headache; muscle problems in mouth; problems in mouth with speech; problems in mouth with speech and swallowing; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (patient) reported that a female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date as a single dose for covid-19 immunisation; hydrocortisone, neomycin sulfate, polymyxin b sulfate (CORTISPORIN), via an unspecified route of administration from an unspecified date at an unknown dose and frequency for an unspecified indictaion. The patient's medical history and concomitant medications were not reported. It was reported that the patient got the vaccine and when the shot was given had a wave of numbness and pressure at the base of her neck and intense head pressure that flared up optic neuritis. Extreme headache and still has it since getting the vaccine on Friday. It caused muscle problems in mouth with speech and swallowing, flared up multiple sclerosis. The outcome of the events was unknown. Information on the lot/ batch number has been requested.

Other Meds: Cortisporin

Current Illness:

ID: 1224478
Sex: F
Age:
State: TX

Vax Date: 03/30/2021
Onset Date: 03/30/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Back pain, Cold sweat, Headache, Nausea, Vomiting

Symptoms: passed out twice; Intense, rapid and irregular heartbeat (prolonged); intense pain in various organs and muscles (some short and some long duration); rash; cold; night sweat; no energy; intense dreams first night; This is a spontaneous report received from a contactable consumer (patient). A 62-year-old female patient (not pregnant) received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) (Lot Number: EP6955) via an unspecified route of administration, administered in arm left on 30Mar2021 13:30 at single dose for COVID-19 immunisation. The patient medical history was not reported. Concomitant medications included zolpidem tartrate (AMBIEN). The patient was healthy. No known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. The patient had not been tested for COVID-19 since the vaccination. The patient received the first dose of BNT162B2 (Lot number: EN6199) in the left arm on 11Mar2021 11:00 AM at the age of 62-year-old for COVID-19 immunisation. The patient experienced passed out twice, intense, rapid and irregular heartbeat (prolonged), intense pain in various organs and muscles (some short and some long duration), rash, cold, night sweat, no energy, intense dreams first night; all on 30Mar2021 with outcome of not recovered. Doctor appointment was scheduled. The events resulted in doctor or other healthcare professional office/clinic visit. It was unknown whether treatment received for the events.

Other Meds: AMBIEN

Current Illness:

ID: 1224479
Sex: M
Age:
State: NY

Vax Date: 03/12/2021
Onset Date: 03/22/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

Symptom List: Injection site swelling, Limb discomfort

Symptoms: tested positive with Covid-19/ he has recovered from the infection and he has no symptoms already; This is a spontaneous report from a Pfizer-sponsored program. A contactable consumer (patient) reported that a male patient of unspecified age received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE) (manufacturer: Pfizer) on 12Mar2021 at single dose for COVID-19 immunisation. Medical history was not reported. Concomitant medications included tetanus vaccine toxoid (TETANUS ADS IMPFSTOFF) on 20Mar2021, measles vaccine, mumps vaccine, rubella vaccine (MMR VACCIN) on 20Mar2021. Patient is due for the second dose of the vaccine tomorrow, 02Apr2021. However, on 22Mar2021, he has tested positive for COVID-19. He said that more or less he has recovered from the infection and he has no symptoms already. He wanted to know if he should be taking it tomorrow or not. Patient also mentioned that on 20Mar2021 he had 2 other vaccines, tetanus and MMR vaccines. Patient asked if they would interfere with bnt162b2. The outcome of the event was recovered. Event was considered serious as medically significant. No follow-up attempts are possible; information about lot/batch number cannot be obtained.; Sender's Comments: Based on the temporal relationship, the association between the event COVID-19 with BNT162b2 can not be fully 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: 1224480
Sex: U
Age:
State: MI

Vax Date: 03/13/2021
Onset Date: 03/20/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: I got symptoms of Covid and tested positive; This is a spontaneous report from a contactable consumer or other non hcp (Patient). A patient of unspecified age and gender received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number) via an unspecified route of administration on 13Mar2021 as single dose for covid-19 immunization. The patient medical history and concomitant medications was not reported. The patient had got first Pfizer shot on March 13th, Saturday and 1 week Later on March 20th I got symptoms of Covid and tested positive, two days later got an antibody infusion. My doctor says get the second shot 2 weeks after I feel 100% or close. The CDC guidelines say "If I got the shot and the antibodies, I should wait 90 Days". The patient underwent lab tests and procedures which included sars-cov-2 test: positive. The outcome of the events was reported as unknown Follow-up activities has been raised. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1224481
Sex: F
Age:
State:

Vax Date: 03/11/2021
Onset Date: 03/13/2021
Rec V Date: 04/18/2021
Hospital:

Vax Type:
Manufacturer:
Vax Name:
Lot:
Dose Series:
Vax Route:
Vax Site:

Lab Data:

Allergies:

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

Symptoms: Covid test and tested positive/feeling a little sick with headache, runny nose and a sore throat; Covid test and tested positive/feeling a little sick with headache, runny nose and a sore throat; This is a spontaneous report from a non-contactable consumer (patient) from a Pfizer-sponsored program. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 11Mar2021 (Batch/Lot number was not reported) as single dose for covid-19 immunization. The patient's medical history and concomitant medications were not reported. The patient received the vaccine on 11Mar2021, the following Saturday (13Mar2021), the patient started feeling a little sick with headache, runny nose and a sore throat. The patient got a covid test and tested positive and then went again on Thursday (15Mar2021) and it came back negative. The patient wanted to know if it has shown positive covid test. The outcome of the events was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

Total 2021 VAERS Injuries: 704,237

Page last modified: 26 October 2021 2:21am