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: 1305038
Sex: M
Age:
State: NC

Vax Date: 01/13/2021
Onset Date: 01/01/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dysphagia, Epiglottitis

Symptoms: shingles; This is a spontaneous report from a contactable consumer (patient). An 83-year-old male patient received the first dose of bnt162b2 (BNT162B2, Solution for injection, Lot Number: EL0140), via an unspecified route of administration, administered in Arm Left on 13Jan2021 (received at the age of 83-years-old) at 0.3 mL, single for COVID-19 immunisation. Medical history included pacemaker and atrial fibrillation. There were no concomitant medications. The patient had his first Pfizer vaccine shot on 13Jan2021 and was scheduled for the second on Wednesday, 03Feb2021. Six or seven days after getting the first dose, in Jan2021, he noticed little red spots. He came down with shingles and his doctor has prescribed him valcyclovir. It's an antiviral medication and he just want to be sure he'll still be able to get the second dose of the vaccine. His physician gave him a miracle medicine for it, Valacyclovir, an antiviral medication, he gathers, and it has done a great job. He has taken it for 3-4 days; the shingles are now leaving. However, he has his next shot, his second shot of the vaccine is this coming Wednesday, and he wondered if anyone at Pfizer can say whether this antiviral for shingles, a pill, is in any way perhaps going to interfere with the COVID second shot. He further stated, "I tell you, that first shot went in like a hot knife through butter!" Outcome of the event was recovering.

Other Meds:

Current Illness:

ID: 1305039
Sex: F
Age:
State: AL

Vax Date: 02/01/2021
Onset Date: 02/01/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Anxiety, Dyspnoea

Symptoms: high blood pressure/blood pressure 167/93/Blood pressure 144/95; Racing pulse/pulse was 177/pulse was 163/Pulse 116/ rapid pulse; Her heart was pounding; she couldn't catch her breath; This is a spontaneous report from a contactable consumer (patient herself). A 43-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL8983, Expiration date: Unknown), via an unspecified route of administration in left arm on 01Feb2021 at 08:45 AM (at the age of 43-year-old) as a single dose for COVID-19 immunization. The patient's medical history included mitral valve prolapse (diagnosed at the age of 18). No known allergies. Concomitant medication included medroxyprogesterone acetate (DEPO PROVERA) from an unspecified date in 2020 and ongoing, received in two weeks within the vaccination. She took a Depo Provera shot on Saturday 30Jan2021, but she has been on this medication for a year now since either Feb2020 or Mar2020. The lot number and expiration date was unknown, since she has discarded the packaging. She usually picks up the drug, and her neighbour was a nurse, she usually just gives her the injection, since COVID has started. The patient previously received flu vaccine on an unspecified date in 2020 for immunisation and experienced feeling bad, didn't feel good. The patient previously received flu vaccine on an unspecified date for immunisation and experienced thrown up, chills, fever, body was sensitive. Caller was queried she if she had had any issues with vaccine in the past, caller states that she takes the flu vaccine every year, her body was sensitive to the flu vaccine, this year she had no issue, but last year (on an unspecified date in 2020) after the flu vaccine she started feeling bad, didn't feel good, years before she has thrown up and had chills and fever. Her body must be sensitive. However she has never had the heart issues. The patient did not receive other vaccine in four weeks. The patient was not diagnosed with COVID-19 prior vaccination. The patient has not been tested with COVID-19 post vaccination. It was reported that, she was calling about the COVID-19 vaccine. She received the vaccine yesterday at 8:45 AM, then at 12:30 PM she began to have a rapid pulse and high blood pressure. She went to the ER because of her pulse and blood pressure. In the ER, she received an IV to calm the heart, she doesn't know what was in the IV. They did blood work and told her the blood work was fine, and the chest X-ray was fine. She went to a Cardiologist today, she does have a valve prolapse, but she has had no issues with that for many years. She states that her body had a weird response to the covid vaccine. Caller states that she need Pfizer to know what happened because it was real scary. She has her first dose on 01Feb2021 at 8:45 AM. The rapid pulse began while she was sitting at the computer working. Her heart was pounding on 01Feb2021, she couldn't catch her breath on 01Feb2021, and so she was a school teacher, so then she went to find the nurse, and even in that she was having trouble catching her breath to be able to even talk. The nurse took her into the office, and she put a pulse ox monitor on her finger. At 12:25 PM her pulse was 177, at 12:30 PM her pulse was 163 with blood pressure 167/93, at 12:40 PM pulse 116, blood pressure 144/95. The nurse then called the ambulance because it was alarming. Caller states that doesn't know what her readings were in the ambulance. She went to the ER at (institute name withheld) and they did an EKG, 2 of them. The regular ER doctor was not super helpful, he said that she was okay to take the second vaccine. Caller did not agree with him thinking that the 1st covid vaccine sent her to the ER. HCP: He was at (institute name withheld) Cardiology. He did an EKG today (on an unspecified date in Feb2021), she doesn't know results at the moment. He didn't say if it was normal or abnormal. They did an echocardiogram, she was also assuming nothing was alarming or she would have been told the results. He listened to the heart and said it sounded fine, there was nothing he could detect. She did have a rapid heart rate at the cardiologist office, both pulse and blood pressure were elevated. He said that she was going to do a stress test in a week, the doctor was also going to see what the blood work from the ER yesterday looks like, he would also check the thyroid. He told her that next week she would also wear a heart monitor. She was at the doctor's office today at 10:30 AM. Her biggest concern was which she talked to the cardiologist today about was the 2nd dose of the vaccine. She doesn't want a repeat of this event. The cardiologist said that she was supposed to get the second dose in 3 weeks, let's do testing and see where we stand. Her 2nd dose was scheduled for 22Feb2021. She was concerned this happened. She doesn't know what could be done. This was bizarre. In the ER, the doctor said this wouldn't be considered an allergic reaction. Caller wonders what this was considered then. The ER doctors thing was that this didn't happen in first 15 to 30 minutes of receiving the vaccine, and that would be considered an allergic reaction if it did. She wants to know if this was an allergic reaction. Enquired was this allergic reaction. The adverse events resulted in emergency room/department or urgent care. She has no results for the tests that were performed at the ER, she was just told the chest X-ray was normal and so was the blood work, but she doesn't know what the blood work involved. They were looking for blood clots at the ER. She was not admitted into the hospital, she was sent home the same day. She has had no positive COVID test prior to the vaccine. She also has had no symptoms, and therefore no reason to get tested either. On 01Feb2021, the patient underwent lab tests and procedure which included chest X-ray: Normal, pulse rapid: 177 (at 12:25 PM), pulse rapid: 163 (at 12:30 PM), blood pressure: 167/93 (at 12:30 PM), pulse rapid: 116 (at 12:40 PM), blood pressure: 144/95 (at 12:40 PM). On an unspecified date in Feb2021, the patient underwent lab tests and procedures which included blood work: Unknown results (the doctor was also going to see what the blood work from the ER yesterday looks like. They were looking for blood clots at the ER), EKG: Unknown results, EKG: Unknown results, Echocardiogram: Unknown results. The patient was treated with IV for the adverse events. The outcome of the events she couldn't catch her breath, her heart was pounding was unknown and not recovered for the other events.

Other Meds: DEPO PROVERA

Current Illness:

ID: 1305040
Sex: F
Age:
State: FL

Vax Date: 02/11/2021
Onset Date: 02/01/2021
Rec V Date: 05/11/2021
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: flu-like symptoms; 102+ degree fever; headaches; body aches; This is a spontaneous report from a Pfizer Sponsored Program. A 74-year-old contactable female consumer reported that she received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number unknown) on 11Feb2021 at single dose for COVID-19 immunization. The patient had received the first dose of vaccine BNT162B2 on 24Jan2021. Medical history included a very rare auto-immune disorder, and strictly limits her contact with other persons. Concomitant drugs were unknown. After receiving the 2nd dose of vaccine she began to experience flu-like symptoms including 102+ degree fever, headaches, and body aches. She is questioning if receiving the vaccine early is what caused her to experience these symptoms since she was scheduled for second dose on 11Feb2021 instead of 14Feb2021. The outcome of the events was unknown. Information about lot/batch number has been requested. Follow-up (07May2021): Follow-up attempts completed. No further information expected.

Other Meds:

Current Illness:

ID: 1305041
Sex: F
Age:
State: NY

Vax Date: 02/05/2021
Onset Date: 02/06/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Dizziness, Fatigue, Mobility decreased

Symptoms: Body aches; Fever; Nausea; Chills; This is a spontaneous report from a contactable consumer (patient). A 66-year-old female non-pregnant patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number: EN5318) via an unspecified route of administration as a single dose in right arm on 05Feb2021 at 17:00 for an COVID-19 immunisation. The patient medical history was not reported. The patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient received concomitant medication (names not specified). The patient did not receive any other vaccine within 4 weeks prior to the vaccine. On 06Feb2021, the patient experienced fever, nausea, chills and body aches. The patient did not receive any treatment for adverse events. The outcome of events was not recovered.

Other Meds:

Current Illness:

ID: 1305042
Sex: F
Age:
State: TX

Vax Date: 02/04/2021
Onset Date: 02/06/2021
Rec V Date: 05/11/2021
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: swelling in the lymph nodes; painful lymph node; This is a spontaneous report from a contactable HCP (patient). A 33-year-old female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: El9264), via an unspecified route of administration, administered in left arm on 04Feb2021 16:00 (at the age of 33-years-old) as single dose for COVID-19 immunisation. The patient took the first dose of BNT162b2 (Lot number: El1283) on 14Jan2021 at 16:00, administered in right arm. The patient did not receive other vaccines in four weeks. Medical history included asthma and allergy to Sulfa. She did not have COVID prior vaccination. Concomitant medications included sertraline, montelukast sodium (SINGULAIR) and chlorphenamine maleate/ibuprofen/phenylephrine hydrochloride (ADVIL ALLERGY AND CONGESTION RELIEF). On 06feb2021 at 08:00 the patient experienced swelling in the lymph nodes in neck and painful lymph node. The patient reported that when she woke up around 08:30 or 09:00 she noticed swelling in the lymph nodes in her neck. The patient stated that they were tender and painful on one side. She stated it was the left side only in which the vaccine was given in her left arm. The swelling was very visible and is where her neck and shoulder meets. The patient did not receive treatment for events, and she was not COVID tested post vaccination. The outcome of events was not recovered. Follow-up attempts are completed. No further information is expected.

Other Meds: SERTRALINE; SINGULAIR; ADVIL ALLERGY AND CONGESTION RELIEF

Current Illness:

ID: 1305043
Sex: F
Age:
State: KY

Vax Date: 02/04/2021
Onset Date: 02/05/2021
Rec V Date: 05/11/2021
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: Injection site turned red, hard and swelled up; Injection site turned red, hard and swelled up; My axilla and peck muscle was swollen to 3 times it's size; feel a big swollen node; Flu type symptoms; This is a spontaneous report from a contactable other-HCP (Patient). A 57-year-old non-pregnant female received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL9269), via unspecified route of administration, administered in left arm on 04Feb2021 at 09:30 AM (at the age of 57-years) as single dose for COVID-19 immunisation. Patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: EL3249), administered at left arm on 12Jan2021 at 09:45 AM as single dose for COVID-19 immunisation. The patient medical history included osteoarthritis. Patient had no known allergies. Concomitant medications included levothyroxine and acyclovir. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. The patient was not diagnosed with COVID-19 prior to vaccination. On 05Feb2021 at 11:30 AM (26-hours after vaccination), patient experienced flu type symptoms and at 09:30 PM (36-hours after vaccine), injection site turned red, hard and swelled up. On 06Feb2021 (morning), axilla and peck muscle swollen to 3 times its size. Patient received ibuprofen and Benadryl for treatment, and it went down a little however, patient can still feel a big swollen node that appeared a day before. No specific treatment was given for swollen node. Since the vaccination, patient was not tested for COVID-19. The outcome of all the events was not recovered.

Other Meds: LEVOTHYROXINE; ACYCLOVIR [ACICLOVIR]

Current Illness:

ID: 1305044
Sex: F
Age:
State: FL

Vax Date: 02/06/2021
Onset Date: 02/06/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Pyrexia, White blood cell count decreased

Symptoms: Profuse Vomiting; chills; dryness; This is a spontaneous report from a contactable Nurse. A 81-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE; Solution for injection; Lot Number: Unknown; Expiry Date: Unknown) dose 1 intramuscular, administered in Arm Left on 06Feb2021 16:00 as SINGLE DOSE for COVID19 immunization. Medical history included If covid prior vaccination: Yes. Concomitant medications included apixaban (ELIQUIS); propranolol; chlorthalidone; pravastatin sodium for an unspecified indication. The patient did not receive any other vaccines within 4 weeks. The patient was diagnosed with COVID-19 prior to vaccination. The patient was not tested positive post vaccination. The patient experienced on 06Feb2021 16:00 profuse vomiting, chills, dryness. The patient did not receive any treatment for adverse event. The outcome of the events were unknown.

Other Meds: ELIQUIS; PROPRANOLOL; CHLORTHALIDONE; PRAVASTATIN SODIUM

Current Illness:

ID: 1305045
Sex: F
Age:
State: TX

Vax Date: 02/03/2021
Onset Date: 02/03/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies: Ct contrast; Dilaudid; Flagyl combined with doxycycline or cephalexin

Symptom List: Pharyngeal swelling

Symptoms: bled a bit; pain in left finger joints/ joint aches; sudden heaviness in arm; chills; severe fatigue; over all unwell/uneasy feeling; Nausea started about the 5th hour; feeling feverish, but never had a real fever; odd little pains in the left side of her neck; tension type headache; foggy; blood vein and possibly a nerve was hit; This is a spontaneous report from a contactable consumer (patient). A 61-year-old female patient (pregnant: No) received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via unspecified route of administration in left arm on 03Feb2021 (lot number: EL9265) at 10:00 at single dose for COVID-19 immunisation. The relevant medical history included arthritis, breathing issues - asthma/copd still being tested, hypertension, liver issues and known allergies: Ct contrast, Dilaudid, Flagyl combined with doxycyline or cephlexinc. Concomitant medications were reported as none. At injection, a blood vein and possibly a nerve was hit. She felt the nurse followed all proper protocol for finishing the injection and notifying RN in charge. On 03Feb2021 at 2:00 PM, the patient had immediate pain in left finger joints and sudden heaviness in arm within a couple of minutes. It bled a bit. She was still having some issues with the hand, but the injection site was fine. She was concerned about the number of symptoms, the severeness and the length of time they had lasted. This was very worrisome and unexpected from all other accounts by others and everything she had read on the first vaccine. She was feeling 'off' within 2 hours, by the 4th hour She had developed chills, severe fatigue and over all unwell/uneasy feeling. Nausea started about the 5th hour and she started feeling feverish, but never had a real fever, odd little pains in the left side of her neck, but that subsided. Developed tension type headache, joint aches, foggy. This continued for about 4 1/2 days. Unable to function without Tylenol every 5hr. Therapeutic measures were taken as a result of the events. The outcome of the events was recovering. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305046
Sex: M
Age:
State: FL

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Abdominal pain, Chills, Sleep disorder

Symptoms: sore arm hours after shot; fatigue/tired; runny nose; coughing/slight cough; This is a spontaneous report from a contactable consumer (patient). An 82-year-old male patient received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number and expiration date unknown) via an unspecified route of administration at left arm 05Feb2021 11:15 (82-year-old at time of vaccination), at single dose, for COVID-19 immunization. The patient's medical history included diverticulitis (surgery), kidney cancer small area excised, and prostate cancer radiated. There were no known allergies. Concomitant medications in two weeks included allopurinol, fenofibrate, tamsulosin, and amlodipine. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, batch/lot number and expiration date unknown) via an unspecified route of administration at left arm on 15Jan2021 11:15 (unknown age at time of vaccination), at single dose, for COVID-19 immunization. There was no other vaccine in four weeks. On 05Feb2021 15:00, patient experienced sore arm hours after shot, fatigue, runny nose, coughing, no temperature the next day. Symptoms abated second day after shot. Still tired and a slight cough. Adverse events did not result in emergency room visit or physician office visit. Patient did not have COVID-19 prior vaccination. Patient did not test for COVID-19 post vaccination. The outcome of the events was recovering. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: ALLOPURINOL; FENOFIBRATE; TAMSULOSIN; AMLODIPINE

Current Illness:

ID: 1305047
Sex: F
Age:
State: MI

Vax Date: 01/14/2021
Onset Date: 01/01/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies: Sulfa

Symptom List: Diarrhoea, Nasal congestion

Symptoms: a full body rash; got itchy all over; This is a spontaneous report from a contactable Other Health Professional (patient). A 54-year-old female patient (not pregnant) received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: FL1283) via an unspecified route of administration at left arm on 14Jan2021 17:00 (54-year-old at time of vaccination), at single dose, for COVID-19 immunization. The patient's medical history included allergies to Sulfa. Concomitant medications in two weeks included estrogen NOS/progesterone patch. The patient previously received amoxicillin and experienced allergies, received nitrofurantoin (MACRODANTIN) and experienced allergies. There was no other vaccine in four weeks. Seven days after the first dose of vaccine (event start date was also reported as 14Jan2021), patient got itchy all over and by the next day, she had a full body rash. She continued to get worse. On day 6 of rash, she went to my doctor and was prescribed steroids. It took 6 days of steroids for the rash to fade. She still have rash, but it is very faded. Adverse event resulted in doctor or other healthcare professional office/clinic visit. Patient had no COVID-19 prior vaccination. Patient did not test for COVID-19 post vaccination. Therapeutic measures were taken as a result of the events and included steroids. The outcome of the events was recovering. Follow-up attempts are completed. No further information is expected.

Other Meds: ESTROGEN NOS;PROGESTERONE

Current Illness:

ID: 1305048
Sex: F
Age:
State: OH

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 05/11/2021
Hospital:

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: My heart was racing.132bpm; I felt lightheaded; tightness in throat; tingling in my arms and hand; This is a spontaneous report from a contactable consumer (Patient). A 42-year-old female patient (not pregnant) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Arm Right on 05Feb2021 15:00 (Batch/Lot number was not reported) at single dose for COVID-19 immunisation. Medical history included known allergies to Pineapple, Bananas, onions, several environmental allergies; asthma. Patient didn't have COVID prior vaccination. Concomitant medications included fexofenadine hydrochloride (ALLEGRA); cromoglicate sodium (ALLERGY) shot; clarithromycin (CLARITIN); mometasone furoate (FLONASE); fluticasone propionate (PROAIR); all taken for an unspecified indication, start and stop date were not reported. No other vaccines were administered in four weeks. Around 8 minutes after vaccine (as reported) patient felt lightheaded, tightness in throat and tingling in her arms and hand. Her heart was racing.132bpm. She told the workers and was taken by ambulance to the hospital. Adverse events start from 05Feb2021 03:15 PM and resulted in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent car. Treatment received included Oxygen, benadryl shot. The outcome of the events was recovering. COVID was not tested post vaccination. No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: ALLEGRA; ALLERGY [CROMOGLICATE SODIUM]; CLARITIN [CLARITHROMYCIN]; FLONASE [MOMETASONE FUROATE]; PROAIR [FLUTICASONE PROPIONATE]

Current Illness:

ID: 1305049
Sex: F
Age:
State: MD

Vax Date: 01/22/2021
Onset Date: 01/01/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies: Verapamil; lisinopril; amlodipine; atorvastatin and experienced drug hypersensitivity with all

Symptom List: Rash, Urticaria

Symptoms: Muscle pain and joint pain 30 minutes after the vaccine; Muscle pain and joint pain 30 minutes after the vaccine; Glucose dropped dramatically after taking my morning metformin after eating; tiredness; headache; chills; nausea; feeling unwell; Soreness at the infection sight for 2-3 days.; This is a spontaneous report from a contactable Consumer (patient, self-reported). A 57-years-old (non-pregnant) female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number- 3302 and expiration date was not reported), via an unspecified route of administration in right arm on 22Jan2021 08:45 (at the age of 57-years-old) as a single dose for covid-19 immunization. The patient was not pregnant at the time of vaccination. Medical history included diabetes mellitus, hypertension. Concomitant medication(s) included calcium carbonate, metformin, hydrochlorothiazide, losartan potassium, spironolactone and colecalciferol. The patient previously took verapamil, lisinopril, amlodipine, atorvastatin and experienced drug hypersensitivity with all. The patient had no other vaccine within four weeks. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. On 22Jan2021 at 09:15, the patient muscle pain and joint pain 30 minutes after the vaccine. In an unspecified date in Jan2021 at 12:30, she experienced soreness at the infection sight for 2-3 days, glucose dropped dramatically after taking morning metformin after eating. Side effects tiredness, headache, chills, joint pain, muscle pain, nausea, and feeling unwell. Soreness at the infection sight for 2-3 days. The patient was treated with 2 ibuprofen. Vaccine facility type: local facility. In Jan2021, the event- soreness at the infection sight for 2-3 days was recovered and outcome of the events was recovered on an unknown date. No follow-up attempts are possible. No further information is expected.

Other Meds: CAL; METFORMIN; LOSARTAN/HCTZ; SPIRONOLACTON; VIT.D3

Current Illness:

ID: 1305050
Sex: F
Age:
State: AR

Vax Date: 02/04/2021
Onset Date: 02/04/2021
Rec V Date: 05/11/2021
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: sore arm; chills; exhaustion so bad it almost bordered nausea; This is a spontaneous report from a contactable consumer or other non-HCP. A 77-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number: EL9264), via an unspecified route of administration in left arm on 04Feb2021 at 07:00 as single dose for covid-19 immunization. The patient medical history and concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. No covid test post vaccination. No other vaccine in four weeks. The patient didn't receive other medication in two weeks. On 04Feb2021 at 22:00, the patient experienced sore arm, chills, and exhaustion so bad it almost bordered nausea. The patient did not receive any treatment for the adverse events. The outcome of events was recovered.

Other Meds:

Current Illness:

ID: 1305051
Sex: F
Age:
State: TX

Vax Date: 01/28/2021
Onset Date: 01/30/2021
Rec V Date: 05/11/2021
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: Tiredness; Headache; Muscle pain; Joint pain; Chills; Fever; Feeling unwell; Cough; loss of appetite; Cataract; 'started feeling really ill'; painful injection site; A 72-years-old female patient who received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/lot number: EL9265, Expiration date: unknown), via an unspecified route of administration on 28Jan2021 in left arm at a single dose for covid-19 immunization. The patient's medical history included asthma, nerve injury, chronic nerve damage and blood pressure measurement. Patients concomitant medications included losartan for blood pressure abnormal at the dose of 100 mg per day, atenolol for blood pressure abnormal, albuterol (SALBUTAMOL)) for asthma at the dose of 1.25mg, esomeprazole sodium (NEXIUM) for gastroesophageal reflux disease. On 02Feb2021, she had a cataract implant on the right side. Which was the side her headaches were on. She didn't know if it was from the vaccine or not. Five days later after surgery, on an unspecified date in Feb2021, the patient experienced started feeling really ill. She was pending a procedure on her other eye as well. She got lots of symptoms. The patient experienced tiredness, headache muscle and joint pain, chills, fever, her injection site was painful, and she was feeling unwell. The patient underwent lab tests and procedures which included body temperature which was 101.2. A couple of days after the vaccine she felt well. On 05Feb2021, then all the sudden she just felt tired and couldn't do anything. She was laying and sitting all day. She had no appetite. It had persisted. She didn't have an appetite when she eats. She couldn't taste the food. She didn't feel as bad. She could feel herself getting better. She was taking more vitamin c and more vitamins. On same date, she had a cough. She had been taking Theraflu and lung support for her chest since she developed the cough. She had fever and which was up to 101.2. It kept fluctuating. This morning it was 96. She had muscle and joint every day, but this was triple the pain of her normal pain. She had been drinking a Gatorade. She took nexium for acid reflux, and she had been taking that for a while. That was why she thinks she couldn't taste as much. She got the vaccine because with everything going on, it was the right thing to do. The reporter assessed cataract as medically significant. The outcome of events tiredness, headache, muscle pain, joint pain, fever, feeling unwell was recovering, while chills, painful injection site were recovered, cough and loss of appetite were not recovered and the outcome of started feeling really ill was unknown. She was scheduled for her second dose on 18Feb2021.

Other Meds: LOSARTAN; ATENOLOL; ALBUTEROL [SALBUTAMOL]; NEXIUM [ESOMEPRAZOLE SODIUM]

Current Illness: Asthma

ID: 1305052
Sex: M
Age:
State: AL

Vax Date: 01/26/2021
Onset Date: 01/29/2021
Rec V Date: 05/11/2021
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: suspected shingles; painful rash; skin burning; The initial case was missing the following minimum criteria: no adverse effect. Upon receipt of follow-up information on (23Mar2021), this case now contains all required information to be considered valid. A 29-year-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration, administered in Deltoid Left on 26Jan2021 15:00 (Lot Number: EL8982; Expiration Date: May2021) as 1ST DOSE, SINGLE for covid-19 immunisation (Age at vaccination: 29 years). The patient's medical history and concomitant medications were not reported. The patient experienced painful rash and skin burning on 29Jan2021 14:00 and he stated that he had suspected shingles on an unspecified date. Outcome of the events was unknown.

Other Meds:

Current Illness:

ID: 1305053
Sex: F
Age:
State: MI

Vax Date: 02/05/2021
Onset Date: 02/01/2021
Rec V Date: 05/11/2021
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: achiness & discomfort at the injection site; achiness & discomfort at the injection site; This is a spontaneous report from a contactable female consumer (patient) via Pfizer-sponsored program. A female patient of an unspecified age received the second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot unknown) on 05Feb2021 at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Previously, on an unspecified date, she received the first dose of the vaccine for covid-19 immunisation.The patient experienced achiness and discomfort at the injection site on Feb2021, non serious and described as follows: she received both inoculations and got the 2nd dose on 05Feb2021. She stated she was currently experiencing side effects like achiness and discomfort at the injection site. The final outcome of the events was reported as unknown. Patient wanted to know if can take Tylenol or Advil and also reported that she put a wrong date on her VSafe. No follow-up attempts are possible, information about batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305054
Sex: F
Age:
State:

Vax Date: 02/05/2021
Onset Date:
Rec V Date: 05/11/2021
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: light headache; back pains; This is a spontaneous report from a contactable consumer (patient), received via the Pfizer-sponsored program. A contactable consumer reported similar events for two patients. This is the first of two reports. A female patient of an unspecified age received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), via an unspecified route of administration on 05Feb2021 (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 experienced light headache and back pains on an unspecified date. The patient stated that she took the vaccine with her husband and they've been taking Tylenol for light headache and back pains. The outcome of 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-2021144715 same reporter/vaccine/events and different patient.

Other Meds:

Current Illness:

ID: 1305055
Sex: F
Age:
State: WA

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

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

Lab Data:

Allergies:

Symptom List: Ear pain, Hypoaesthesia

Symptoms: Urinary tract infection after the 1st vaccine; This is a spontaneous report from a contactable consumer (Patient) via Pfizer Sponsored Program. A female patient of an unspecified age received first dose of BNT162B2 (Pfizer Covid-19 Vaccine, Solution for injection, Lot# unknown), via an unspecified route of administration on an unspecified date as a single dose for COVID-19 Immunization. Medical history and concomitant medications were not reported. On an unspecified date patient experienced urinary tract infection after the 1st vaccine. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1305056
Sex: F
Age:
State: AZ

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

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

Lab Data:

Allergies:

Symptom List: Abdominal pain upper, Dizziness, Dysgeusia

Symptoms: 5 days after vaccination experiencing seasonal allergies; This is a spontaneous report from a Pfizer sponsored program via a contactable consumer (patient). A female patient of an unspecified age received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; Solution for injection), via an unspecified route of administration on an unspecified date as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date the patient took 2nd dose and 5 days after vaccination was experiencing seasonal allergies. The outcome of the event was unknown. Information about lot/batch has been requested.

Other Meds:

Current Illness:

ID: 1305057
Sex: F
Age:
State:

Vax Date: 02/06/2021
Onset Date: 02/01/2021
Rec V Date: 05/11/2021
Hospital:

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: is now showing some red rashes. Got in both arms, greased in elbow; This is a spontaneous report from a Pfizer-sponsored program. A non-contactable female consumer (patient). A female patient of unspecified age had received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Formulation: Solution for injection, Lot number: unknown), via an unspecified route of administration on 06Feb2021 as single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Patient had stated that after 2nd dose of vaccine yesterday, approximately on unknown date in Feb2021, (reported as now) showing some red rashes. Got in both arms, greased in elbow. Patient wants to let us know about this if this is okay. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Other Meds:

Current Illness:

ID: 1305058
Sex: M
Age:
State: NC

Vax Date: 01/11/2021
Onset Date: 02/06/2021
Rec V Date: 05/11/2021
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: shingles/ Between Saturday and Sunday I came up with I guess a small amount of the doctor said maybe shingles; This is a spontaneous report from a contactable consumer (patient) from a Pfizer-sponsored program. A 70-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, lot number and expiry date not reported), via an unspecified route of administration on 11Jan2021 as a first dose, single for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. Patient was asking if he can take the second shot after getting shingles from 06Feb2021. He got the first dose last 11Jan2021 and supposedly to take the second one tomorrow (11Feb2021). Patient asked if the COVID-19 vaccine was the reason behind his shingles. Between Saturday and Sunday, 06Feb2021 and 07Feb2021, patient came up with what he guessed was a small amount of the doctor said maybe shingles. It was then reported that patient was scheduled/supposed to get second Pfizer-Biontech Covid-19 vaccine at the time of the report (11Feb2021) at 10am. He planned to contact his physician, before his appointment, so was not transferred to Safety. Patient was being alright, he was just seeing those on his shoulder and everything. He was just calling to see would it be alright for him to take that second shot on 11Feb2021 if it was shingles. The outcome of the event was unknown. Information about the Lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1305059
Sex: M
Age:
State: VA

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

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

Lab Data:

Allergies:

Symptom List: Unevaluable event

Symptoms: colds; chills; body ache; This is a spontaneous report from a consumer (patient) via a Pfizer-sponsored program. A male patient of an unspecified age received first dose of BNT162B2 (solution for injection, Lot number: unknown), via an unspecified route of administration on an unknown date, as a single dose for Covid-19 immunization. Medical history and concomitant medications were not reported. On an unspecified date, the patient experienced side effects such as colds, chills, and body ache. The outcome of the events was unknown. Information on lot & batch number of the suspect drug if available.

Other Meds:

Current Illness:

ID: 1305060
Sex: F
Age:
State: GA

Vax Date: 02/04/2021
Onset Date: 02/04/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies: Penicillin

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

Symptoms: Lightheaded/feeling dizzy; BP 168/68, BP 158/73, BP 152/73; O2 SAT 97%, O2 SAT 96%, O2 SAT 97%; HR 62, HR 68, HR 69; This is a spontaneous report from a contactable Other HCP. This Other HCP reported for a 79-year-old non-pregnant female patient who received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), Solution for injection, Batch/lot number: el3302, Expiration date: unknown), via an intramuscular route of administration in left arm on 04Feb2021 at 09:19 at a single dose for covid-19 immunization in clinic (at the age of 79-years). The patient had rash to PCN (penicillin). The patient's medical history included HTN (hypertension) and concomitant medication included lisinopril for an unspecified indication on an unspecified date. The patient did not have any other illness at the time of vaccination and up to one month prior. Patient's vital signs were taken three times. On 04Feb2021 at 09:36, the patient experienced feeling lightheaded, BP (blood pressure) 168/68, BP 158/73, BP 152/73, oxygen saturation 97%, O2 SAT 96%, O2 SAT 97% and HR (heart rate) 62, HR 68, HR 69. Patient given water. After 20 minutes the patient stated feeling dizzy but wanted to leave. The outcome of events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds: LISINOPRIL

Current Illness:

ID: 1305061
Sex: F
Age:
State: NY

Vax Date: 02/06/2021
Onset Date: 02/06/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies: Sulfa and ceclor

Symptom List: Injection site pain, Pain

Symptoms: Low grade fever; strong muscle aches; still cannot sleep.; This is a spontaneous report from a contactable consumer, the patient. A 67-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection, Lot number: EM9810, Expiration Date: unknown), dose 2 via an unspecified route of administration, administered in Arm Left on 06Feb2021 10:00 as single dose for covid-19 immunisation. Medical history included osteoporosis, BRCA 2. patient had known allergies for Sulfa and ceclor. Concomitant medication included estradiol. The patient previously took first dose of the BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot Number EL3247), via an unspecified route of administration, on right arm on 15Jan2021 04:30 PM at single dose for COVID-19 immunization. On 06Feb2021 22:00, patient experienced Low grade fever and strong muscle aches throughout body that were so bad as she has not been able to sleep. Patient was not pregnant at the time of vaccination. Patient did not received treatment for the adverse event Patient did not received any other vaccines within 4 weeks prior to the COVID vaccine. Patient was not diagnosed with COVID-19 Prior to vaccination. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events was recovered with sequelae.

Other Meds: ESTRADIOL

Current Illness:

ID: 1305062
Sex: M
Age:
State: MT

Vax Date: 01/30/2021
Onset Date: 02/09/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Injection site pain, Menorrhagia

Symptoms: I contracted Covid 10 days after being vaccinated; This is a spontaneous report received from a contactable 57-year-old male consumer (patient) and contactable other health professional. This patient reported for himself that he received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection), via an unspecified route of administration on 30Jan2021 at 14:15 (age at vaccination 57 years) at single dose in left arm for covid-19 immunization. The patient administered vaccine at hospital. The patient's medical history included graves disease and myasthenia gravis. Concomitant medications included levothyroxine and eszopiclone (LUNESTA). On 09Feb2021 at 10:00, the patient had contracted with Covid-19. The patient experienced the event at Doctor or other healthcare professional office/clinic visit. The patient did not take any treatment for the event. The patient laboratory details included PCR and nasal swab both on 09Feb2021 with positive results. Upon follow up on 22Mar2021, it was reported that the patient contracted COVID after first shot. The outcome of the event was not recovered. The Other health professional considered (reporter) that the Pfizer product had a no causal effect to the adverse event. Follow-up (22Mar2021): New information received from a contactable other HCP. This other HCP reported in response to HCP letter sent which included: Clinical information added No follow-up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds: LEVOTHYROXINE; LUNESTA

Current Illness:

ID: 1305063
Sex: F
Age:
State: TX

Vax Date: 02/10/2021
Onset Date: 02/11/2021
Rec V Date: 05/11/2021
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: swollen lymph node glands size of golf ball very tender to touch; Body aches; Vaccine arm swelling sore and swollen; Vaccine arm swelling sore and swollen; Headaches; This is a spontaneous report from a contactable consumer(patient). A 63-years-old female patient received bnt162b2 (BNT162B2, solution for injection, Batch/Lot Number: EL9266 ), second dose via an unspecified route of administration, administered in right arm on 10Feb2021 17:15 (Batch/Lot Number: EL9266) as SINGLE DOSE for covid-19 immunization. Medical history included high blood pressure and anemic, both from an unknown date and unknown if ongoing. On 25Jan2021 at 5:30 PM patient received first of Bnt162b2 (lot number=EL9262) in right arm. No COVID was found prior vaccination. Other medications were taken in two weeks but not specified. Concomitant medications were not reported. On 11Feb2021 at 7:00 PM the patient experienced swollen lymph node glands size of golf ball very tender to touch, body aches, vaccine arm swelling sore and swollen and headaches. Outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 1305064
Sex: F
Age:
State: IA

Vax Date: 02/09/2021
Onset Date: 02/01/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea, Pain in extremity, Pyrexia

Symptoms: hands are tingly; My hands are tingly and so cold.; felt terrible everyday; Nauseated; Arms felt like they were asleep; so sick; Hurt all over; not moving too fast; I do not want food; I have not eaten, taken a shower or anything; This is a spontaneous report from a contactable consumer (Patient, self-reported). A 80-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number was not reported), dose 1 via an unspecified route of administration on 09Feb2021 09:45 (at the age of 80-years-old) as SINGLE DOSE for covid-19 immunisation. Medical history included immunodeficiency, atrial fibrillation. The patient got her shot last Tuesday morning at 9:45 and had been real sick after this. The patient had a bad reaction to it. Well after patient got the shot it was in the. And it said if she was on blood thinner (Unspecified Medications) or 'immune disorder' (not clarified further) she know and she was both of those and was just wondering what to expect and today from elbow. On unspecified date of Feb2021 , her arms felt like they were asleep and then now it was from elbow bit down and her hands got real cold. Now she had not ran a fever and she had not vomited, but she did not want food. She had hurt all over and she had been nauseated (on unspecified date of Feb2021) but not vomited. She had not eaten, taken a shower or anything, and she had been so sick (on unspecified date of Feb2021). Well let her see if she could see a pen that writes. She was not moving too fast (on unspecified date of Feb2021). She wanted to know if this was going to affect her blood, the thickness or the firmness. Since Tuesday, 09Feb2021, patient hands were tingly and so cold. The patient had felt terrible everyday. She had other relatives that got some aches and fatigue , but nothing like what she had. The patient was not currently not taking any immunosuppressant drugs. Patient was enquiring that was it ok to get her 2nd Pfizer vaccine vaccine dose in 4 weeks. The patient also enquiring about was it a problem, with getting the vaccine, if she take Blood thinners, she had atrial Fib and used to get a lot of blood clots. And was there any problem with being immunocompromised and getting the vaccine. Outcome of the events was unknown. Information on batch/lot number has been requested. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1305065
Sex: F
Age:
State:

Vax Date: 01/27/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Chills, Fatigue, Headache, Myalgia

Symptoms: pain, swelling, mild redness of lower lip; pain, swelling, mild redness of lower lip; pain, swelling, mild redness of lower lip; This is a spontaneous report from a non-contactable consumer. A 54-years-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: EL3249) via unspecified route of administration on 27Jan2021 as single dose for COVID-19 immunization. The patient Medical history included Hypertension, allergic rhinitis. Patient had no known allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient Concomitant medication included fexofenadine hydrochloride (ALLEGRA), famotidine (PEPCID [FAMOTIDINE]), hctz (HCTZ), magnesium oxide (MAG OXIDE), multivitamins within 2 weeks of vaccination. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: EK5730) via unspecified route of administration on 06Jan2021 as single dose for COVID-19 immunization. After first dose, the patient experienced brief, intermittent sharp pain on Right side of mouth, lasted 2 days. The patient has not received any other vaccines within 4 weeks prior to the COVID vaccine. On an unspecified date, the patient experienced pain, swelling, mild redness of lower lip and lasted 2-3days. The Patient didn't received treatment for the events. The clinical outcome of events was recovered. No follow-up attempts are possible; information about lot/batch number cannot be obtained.

Other Meds: ALLEGRA; PEPCID [FAMOTIDINE]; HCTZ; MAG OXIDE

Current Illness:

ID: 1305066
Sex: F
Age:
State: TX

Vax Date: 01/18/2021
Onset Date: 01/25/2021
Rec V Date: 05/11/2021
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: extreme itching in hands, feet, scalp; no appetite for 2 weeks; This is a spontaneous report from a contactable Other Health Professional. A 52-year-old (non-pregnant) female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection; Lot Number: Unknown; Expiry Date: Unknown), via an unspecified route of administration in left arm on 18Jan2021 as single dose for COVID-19 Immunization. The patient's medical history included known allergies. Concomitant medications were not reported. The patient previously received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE; solution for injection; Lot Number: Unknown; Expiry Date: Unknown), via intramuscular rote of administration in left arm on 28Dec2020 at 05:15 PM as single dose for COVID-19 Immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and post vaccination not tested COVID. The patient experienced Severe fatigue, and no appetite for 2 weeks, now those symptoms are better but now have extreme itching in hands, feet, scalp on 25Jan2021. It is unbearable, and have been on Medrol dose pack, now Atarax, and prednisone (higher dose) and still have uncontrollable itching with only relief at night. Also have welps that come up. So we are now on 3 weeks with no relief from the 2nd part of the vaccine. The patient received any treatment for adverse event (Prednisone, steroid shot and Medrol dose pack). The clinical outcome of the event no appetite for 2 weeks was recovering and the outcome of the event extreme itching in hands, feet, scalp was not recovered.

Other Meds:

Current Illness:

ID: 1305067
Sex: U
Age:
State:

Vax Date: 02/06/2021
Onset Date: 02/07/2021
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies:

Symptom List: Nausea

Symptoms: Fever; arm pain - unable to lift arm that was injected; Chills; Very bad headache; Body Aches; Extreme exhaustion - slept all day; This is a spontaneous report from a contactable consumer (patient, self-reported). A patient of an unspecified age and gender received second dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not provided), via an unspecified route of administration, in unspecified arm, on 06Feb2021, as a single dose for COVID-19 immunization. The patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not provided), via an unspecified route of administration, on an unknown date, as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that Sunday on 07Feb2021, the patient had chills, very bad headache, body aches, extreme exhaustion - slept all day, fever sunday night around 8:30 PM EST - 100 / 101 F - broke around at 3 AM, and arm pain - unable to lift arm that was injected. The patient woke up this morning Monday 08Feb2021 and feeling much better than the patient did. Outcome of the events was recovering. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1305068
Sex: F
Age:
State: MI

Vax Date: 01/22/2021
Onset Date:
Rec V Date: 05/11/2021
Hospital:

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

Lab Data:

Allergies: Peppermint

Symptom List: Injection site pain

Symptoms: Headache; Light head; This is a spontaneous report from a contactable consumer (patient). This 52-year-old non-pregnant female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL3248 and expiry date was not reported) via an unspecified route of administration in arm Left on 22Jan2021 14:45 as single dose for COVID-19 immunisation. The patient's medical history included Asthma, eczema and Known allergies to Peppermint. The patient's concomitant medications included montelukast at 10 mg, loratadine at 10 mg and cyclobenzaprine. Patient was not diagnosed with COVID prior vaccination. The patient was not tested for COVID post vaccination. The patient did not receive other vaccine in four weeks of vaccine. The patient experienced headache and her head was light on an unknown date in 2021. No treatment was given for the events. Outcome of the events was recovering.

Other Meds: MONTELUKAST; LORATADINE; CYCLOBENZAPRINE

Current Illness:

ID: 1305069
Sex: M
Age:
State: NJ

Vax Date: 01/27/2021
Onset Date: 02/08/2021
Rec V Date: 05/11/2021
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Symptom List: Injection site induration, Injection site pruritus, Injection site swelling, Injection site warmth

Symptoms: swelling and it felt numb, the numb feeling starting on left side of cheek and wound up settling in upper lip; swollen gland he noticed on the left side; the swelling in the mouth on the 11Feb2021 on his lip lasted about 2 days,his upper lip irritated on inside for a day or 2,; swelling that occurred in his mouth/1st occurrence of swelling was like golf ball size, it was visible; This is a spontaneous report from a contactable consumer (patient). A 79-years-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EL3248), dose 1 via an unspecified route of administration, administered in Arm Left on 27Jan2021 11:00 (at 79-years age) as single dose for covid-19 immunisation. Medical history included diabetes and hypertension (he was diabetic and was on blood pressure medication, but both his hypertension was under control, and his diabetes, sure his A1C is higher than it should be but was under control with oral medication), root canal infection (though this was contributed to the root canal which he had on 29Jan2021, the root canal was on the lower left of the mouth, tooth number 20). Patient provided relevant Family medical History of Hypertension. Concomitant Medications: He was just taking his general medications, like his maintenance medication, nothing out of the normal. He had no other vaccines on the same day as the covid vaccine or in the 4 weeks prior. He had no positive covid or antibody test prior to the first dose (he had never had a test).On 08Feb2021, the patient had the 1st occurrence of swelling was like golf ball size, it was visible, but it went away after 3-4 hours and he didn't have to take anything. Then on the 11Feb2021, the patient woke up at 4:30AM, experienced the swelling and it felt numb, the numb feeling starting on left side of cheek and wound up settling in upper lip, it gave him a distorted appearance, it was severe. The swelling in the mouth, that wound up settling in upper lip which was the 2nd occurrence in a 3-day period. The first occurrence was swelling, not as severe, in the lower inside of the mouth in the lower right inside of the gum, the swelling appearance from the outside, though this was contributed to the root canal (had on 29Jan2021). The swelling in the mouth from 08Feb2021 subsided for him in 3-4 hours. He called endodontist, and told her about the second swelling, she said to come in and look at it, that was on 11Feb2021, she took X-rays and result was normal, she said it was not connected to the root canal and told him to contact his Primary and go from there, he agreed with her because he did not feel any type of sensitivity. On 11Feb2021, patient then called the Primary Care doctor, told how he developed the swelling, and the primary care said that he would rather see an ENT specialist and he got an appointment with the ENT that same day 11Feb2021 at 15:00 in the afternoon. The patient went to see him, the ENT checked his mouth out, checked his nose and throat, he did not know what it was stemming from, and said he will put him on an antibiotic. On 11Feb2021, the ENT said that the patient did had a swollen gland he noticed on the left side. The swelling in the mouth on the 11Feb2021 on his lip lasted about 2 days, his upper lip irritated on inside for a day or 2, but it lasted till about the 13Feb2021. On 11Feb2021 (5 days ago), the patient was put on an antibiotic for swelling that occurred in his mouth which was Clindamycin HCL 300mg, 3 pills a day with his last 2 pills of antibiotics falls same day (18Feb2021) as his second vaccine dose was scheduled on Thursday (18Feb2021; appeared to be scheduled outside of the 21-day recommendation). Patient felt like he was sort of on edge for another occurrence possibly happening. Being on the antibiotic, maybe this was some type of infection. The ENT told honestly that he didn't know why this happened, but if it happened again, he might have a CT scan for the suspect salivary gland, maybe it was clogged or there was an infection in the gland. He asked if he should take the pills or reschedule the vaccine dose and if it was ok to receive the second shot while on this antibiotic (his prescribing doctor couldn't give an answer). On 18Feb2021, the patient was due to have booster. Patient would have 2 pills left on the 18Feb2021, after that he was finished. Therapeutic measures of antibiotic were taken as a result of swelling that occurred in his mouth (mouth swelling). He did not have to go to the emergency room for the mouth swelling but he has visited the physician's office. The outcome for swelling in the mouth and lips was recovered on 13Feb2021 (Duration 5 Day); outcome for swollen gland was unknown. Follow up (16Feb2021): This is a follow up spontaneous report from a contactable consumer. This consumer reported patient information, new event information.

Other Meds:

Current Illness:

ID: 1305070
Sex: M
Age:
State: FL

Vax Date: 02/09/2021
Onset Date: 02/09/2021
Rec V Date: 05/11/2021
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Symptom List: Chills, Dizziness, Nausea, Pain, Tachycardia

Symptoms: extreme sweating; Severe Chills; Muscle Ache; Ear Ache; This is a spontaneous report from a contactable consumer. A 73-year- old female consumer received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: unknown), via an unspecified route of administration administered on arm left on 09-FEB-2021 09:30 as a single dose for covid-19 immunisation. Historical vaccine included first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Batch/Lot Number: unknown), via an unspecified route of administration on 19Jan2021 11:15 AM as a single dose for covid-19 immunisation. The patient medical condition included moderate Cholesterol. There were no known allergies. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Concomitant medication included statin. On 09 Feb2021, at 8:00pm the patient had experienced Severe chills, muscle ache, extreme sweating, and ear ache. No treatment was received in response to the adverse events. The patient was not diagnosed with COVID-19 prior to vaccination. Since the vaccination, patient was not tested for COVID-19. On an unspecified date, the events were resolved. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1305071
Sex: F
Age:
State: AK

Vax Date: 01/01/2021
Onset Date:
Rec V Date: 05/11/2021
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Symptom List: Tremor

Symptoms: was not feeling well; Little bit of the fever; Came down with the sniffles; This is a spontaneous report from a contactable consumer (patient's husband). This is the second case out of two cases in which reporter was reporting for his wife. A 67-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: EN5318 and Expiration date was not reported), via an unspecified route of administration, in Deltoid Left, on an unknown date in Jan2021 as a single dose for COVID-19 immunisation. Medical history included ongoing blood pressure abnormal, Migraine and scoliosis (further clarification about scoliosis was unknown). Concomitant medications included regular pain medication because she has got scoliosis, paracetamol (TYLENOL) and ibuprofen (ADVIL), regular blood pressure medication and medications for Migraine only when it was. It was stated that reporter (patient's husband) and patient both received the first doses of the COVID 19 vaccine a little over 3 weeks ago (in Jan2021) and were scheduled to receive the second dose of the vaccine on 12Feb2021. On Wednesday, his wife came down with the sniffles and on Thursday she was not feeling well and had Little bit of the fever; all were on an unspecified date in 2021. So cancelled their second dose appointments and waiting to get another appointment for their second doses through their insurance. Reporter's daughter is a nurse and told them they only have a 4 day window to receive the second dose of the vaccine in regards to safety. They are going to be getting their second doses of vaccine past the 21 days period; It has already been four days after we were supposed to have the shot. No treatment was received for the events. Outcome of events was reported as not recovered.

Other Meds: TYLENOL; ADVIL [IBUPROFEN]

Current Illness: Blood pressure abnormal

ID: 1305072
Sex: M
Age:
State: CA

Vax Date: 02/11/2021
Onset Date: 02/12/2021
Rec V Date: 05/11/2021
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Allergies: NSAIDS

Symptom List: Erythema, Pruritus

Symptoms: Chills; fever; headache; muscle aches; pains; This is a spontaneous report from a contactable consumer (patient). A 73-year-old male patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: El9262), via an unspecified route of administration, administered in left arm on 11Feb2021 at 09:30 (at the age of 73 years old) as a single dose for COVID-19 immunisation. Medical history included lung cancer, allergic to NSAIDS. No concomitant medications were reported. Other medication in two weeks includes included one a day vitamin. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. The patient previously received first dose of BNT162B2 (PFIZ-ER-BIONTECH COVID-19 VACCINE, Lot number: Not reported) in left arm on 22Jan2021 at 10:00 for COVID-19 immunisation. On 12Feb2021 at 12:30 the patient experienced, chills, fever, headache, muscle aches and pains. The patient did not receive any treatment for the events. The outcome of the events was recovered on an unspecified date in 2021.

Other Meds:

Current Illness:

ID: 1305073
Sex: F
Age:
State: NY

Vax Date: 02/15/2021
Onset Date: 02/15/2021
Rec V Date: 05/11/2021
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Symptom List: Injection site erythema, Injection site induration, Injection site pruritus, Injection site swelling, Myalgia

Symptoms: Soreness at site; stiffness raising arm; fatigue; headache; nausea; chills; This is a spontaneous report from a contactable consumer (patient). A 74-year-old non- pregnant female patient received BNT162B2 (Pfizer vaccine COVID 19, Solution for injection, Lot number: EL9266 and expiry date was not reported), via an unspecified route of administration in the Arm Right on 15Feb2021 at 10:45 AM (at the age of 74-years-old) as a single dose for COVID-19 immunisation. The patient's medical history had Known allergies (unspecified). The patient's concomitant medications were not reported. Patient didn't receive any other vaccination within 4 weeks of vaccination. Patient received other medications (unspecified) in 2 weeks of vaccination. Patient had no COVID prior vaccination and not tested for COVID post vaccination. On 15Feb2021 the patient experienced Soreness at site and stiffness raising arm, fatigue, headache, nausea, and chills. No treatment was taken for the events. The clinical outcome of the events was recovering.

Other Meds:

Current Illness:

ID: 1305074
Sex: F
Age:
State: IN

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 05/11/2021
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Allergies: Penicillin; sulfa; dairy

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

Symptoms: Reactions were arm sore; Tiredness; Body ache; headache; This is a spontaneous report from a contactable consumer (patient). A 90-years-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number: Unknown) dose 2 via an unspecified route of administration, administered in right arm on 05Feb2021at 15:30 as single dose for covid-19 immunization. historical vaccine include dose 1 via an unspecified route of administration, administered on 14Jan2021, (at the age of 90 years-of-old). Medical history included Heart failure, Chronic high blood pressure, Obesity, Kidney Disease, penicillin, sulfa, dairy allergies. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. Concomitant medications included Aldactone, Bystolic, Lisinopril, Zetia, and Cymbalta. The patient stated that 1st Dose was on 14Jan2021, of Pfizer Vaccine did NOT produce any side effects that she was aware of. However, the 2nd Dose on 05Feb2021 07:00pm, of Pfizer Vaccine produced side effects about 3 hours after the injection. Reactions were arm sore, tiredness, body ache, head-ache; no diarrhea, temp not taken and went to bed and slept. These side effects continuing February 6 and February 7. On February 7 took Tylenol to help with aches and pains. She stated that the side effects were continuing. The outcome of the events was reported as not recovered. Information on the Lot/Batch number has been requested. Follow-up attempts are completed. No further information is expected

Other Meds: CYMBALTA; ZETIA; LISINOPRIL; BYSTOLIC; ALDACTONE [SPIRONOLACTONE]

Current Illness:

ID: 1305075
Sex: F
Age:
State: VA

Vax Date: 02/03/2021
Onset Date: 02/03/2021
Rec V Date: 05/11/2021
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Symptom List: Asthenia, Chills, Headache, Myalgia

Symptoms: I started having parathesoas of bilateral lower extremities the evening of my second dose.; The next day I saw my pop and my pulse and blood pressure were elevated.; The next day I saw my pop and my pulse and blood pressure were elevated.; I am also having headaches; stuffy nose; sinus pressure; brain fog; my vision is blurry; tinnitus; This is a spontaneous report from a contactable Nurse (Patient). This 68-year-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number: Ec3302) via an unspecified route of administration, administered in left arm on 03Feb2021 at 08:15 AM (at the age of 68-years-old) as single dose for COVID-19 immunisation. Patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number: EI8982) via an unspecified route of administration, administered in left arm on 15Jan2021 at 08:00 AM as single dose for COVID-19 immunisation. Patient received no other vaccine in four weeks prior vaccination and was not tested for COVID prior vaccination. The patient medical history included known allergies like airborne allergies, grasses, molds, trees, pollen, dust and had controlled hypertension. Concomitant medications included Losartin 50 mg. On 03Feb2021 (at evening, same day of vaccination), patient started having parathesias of bilateral lower extremities. Patient saw pop and pulse rate and blood pressure were elevated. This had continued for the past five days. Patient also had headaches, stuffy nose, sinus pressure, brain fog, vision was blurry and tinnitus. Patient not tested for COVID post vaccination. Outcome was not recovered for all the events.

Other Meds: LOSARTIN

Current Illness:

ID: 1305076
Sex: F
Age:
State:

Vax Date: 01/12/2021
Onset Date: 02/04/2021
Rec V Date: 05/11/2021
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Symptom List: Injection site erythema, Injection site pain, Injection site swelling

Symptoms: Muscle ache, joint pain, chills, hot flashes, migraine; Muscle ache, joint pain, chills, hot flashes, migraine; Muscle ache, joint pain, chills, hot flashes, migraine; Muscle ache, joint pain, chills, hot flashes, migraine; Muscle ache, joint pain, chills, hot flashes, migraine; This is a spontaneous report from a non-contactable other hcp. A 27-years-old non-pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number was not reported), intramuscular, administered in Left Arm on 12Jan2021 07:30 as single dose for covid-19 immunization. Medical history included, food allergy; Known allergies: Ceclor, peanuts. There were no concomitant medications. The patient previously took ceclor and experienced drug hypersensitivity. The patient previously took BNT162B2 on an unspecified date. The patient did not receive any other vaccine in four weeks. The patient did not have COVID prior vaccination and post vaccination, patient had not tested with covid 19. On 04Feb2021 11:00 the patient experienced muscle ache, joint pain, chills, hot flashes, migraine. No treatment was received for these events. 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: 1305077
Sex: F
Age:
State: ID

Vax Date: 01/28/2021
Onset Date: 01/28/2021
Rec V Date: 05/11/2021
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Symptom List: Chills, Feeling cold, Feeling hot, Myalgia, Pain

Symptoms: Uncontrollable chills; body aches; lower and frontal headache; upper back pain; neck pain; hives on legs; This is a spontaneous report received from a non-contactable other hcp. A 26-years-old non-pregnant female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: EN5318), intramuscular on 28Jan2021 as single dose for COVID-19 immunization. Medical history included COVID-19 from an unknown date and unknown if ongoing. Concomitant medications were not reported. The patient did not receive any other vaccine in four weeks. The patient did not have any known allergy. Post vaccination, the patient not tested for COVID. On 28Jan2021, patient experienced uncontrollable chills, body aches, lower and frontal headache, upper back pain, neck pain and hives on legs. It was unknown if the patient received any treatment for AE. The symptoms lasted for 2-3 days and approximately on an unknown date in 2021, patient recovered from all events. No follow up attempts are possible. Information about Lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1305078
Sex: M
Age:
State: CA

Vax Date:
Onset Date:
Rec V Date: 05/11/2021
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Symptom List: Pain in extremity

Symptoms: Shingles; This is a spontaneous report from a Pfizer-sponsored program. A contactable nurse reported that a male patient of an unspecified age (reported as 58) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection), dose 1 via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced shingles 4 days before the 2nd dose. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot been obtained

Other Meds:

Current Illness:

ID: 1305079
Sex: F
Age:
State: FL

Vax Date: 02/02/2021
Onset Date: 02/03/2021
Rec V Date: 05/11/2021
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Symptom List: Abdominal pain upper, Abnormal behaviour, Adverse reaction, Anger, Asthma

Symptoms: Large hot, red, raised oval shaped swelling; Large hot, red, raised oval shaped swelling; Large hot, red, raised oval shaped swelling; This is a spontaneous report from a contactable consumer. A 74-year-old female non pregnant female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, lot number: EL9263), via an unspecified route of administration in the left arm on 02Feb2021at 09:00 AM (at the age of 74-year-old) as a single dose for COVID-19 immunisation. Medical history included patient had Codeine allergy. Concomitant medications included atorvastatin (LIPITOR [ATORVASTATIN]), ciclopirox, calcium, vitamin d nos, vitamin b complex (VITAMIN B) (all received in two weeks). The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, solution for injection, lot number: EL3246), via an unspecified route of administration in the left arm on 12Jan2021 at 09:00 AM as a single dose for COVID-19 immunisation. On 03Feb2021 at 08:00 AM, patient experienced Large hot, red, raised oval shaped swelling. No treatment was received for adverse events. Outcome for the events was recovered on an unspecified date in 2021.

Other Meds: LIPITOR [ATORVASTATIN]; CICLOPIROX; CALCIUM; VITAMIN D NOS; VITAMIN B

Current Illness:

ID: 1305080
Sex: F
Age:
State: CA

Vax Date: 01/27/2021
Onset Date: 01/29/2021
Rec V Date: 05/11/2021
Hospital:

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

Symptoms: green stools; difficulty breathing; nausea; headache; dizzeyness; loss of appetite; This is a spontaneous report from a contactable consumer (patient herself). A 62-years-old female patient (who was not pregnant at the time of vaccination), received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot Number: paa156051), dose 1 via an unspecified route of administration, in Arm Left, on 27Jan2021 12:30pm as single dose for covid-19 immunisation. Vacination facility was Other. Medical history included High blood pressure, Low potassium and High cholesterol. The patient had no allergies. Concomitant medication's included Lisinopril, potassium and simvastatin. Patient did not receive other vaccine in four weeks of vaccination. Patient was not diagnosed with COVID, prior vaccination. The patient previously reported her adverse events but forgot to add that on 29Jan2021 at 06:00pm she have had green stools since the vaccine along with the 3 episodes of difficulty breathing, nausea headache dizzeyness and loss of appetite this was from wed of injection until friday 9 days later. The patient was terrified of receiving the second dose because these symptoms happened on the 3rd day and later. If she does not take the second dose what are my chances of surviving the virus if she should come down with it. She tried calling and was on hold for 4 hours and no one picked up. Events resulted in emergency room. The patient underwent lab tests and procedures after vaccination which included COVID-19 (sars-cov-2) test: negative on 05Feb2021. Patient did not received any treatment for the events. Outcome of the events was recovering. Follow-up attempts are completed. No further information is expected.

Other Meds: LISINOPRIL; POTASSIUM; SIMVASTATIN

Current Illness:

ID: 1305081
Sex: F
Age:
State: OH

Vax Date: 02/06/2021
Onset Date: 02/07/2021
Rec V Date: 05/11/2021
Hospital:

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

Symptoms: Ear ache; Fever of 102+; Headache; Chills; This is a spontaneous report from a contactable Consumer (Patient). A 26-year-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot# unknown), via an unspecified route of administration on 06Feb2021 at 11:45 (at the age of 26-years) as single dose for Covid-19 immunization. The patient medical history and concomitant medications were not reported. Patient had COVID prior vaccination on an unspecified date. Patient received no other vaccine in four weeks. On 07Feb2021 at 01:00 (one day after vaccination), patient experienced fever of 102+, headache, ear ache, chills. No therapeutic measures were given for any of events. Patient underwent lab test: body temperature: fever of 102+ on 07Feb2021. Patient had no COVID tested done post vaccination. The outcome of all the events was not recovered. Information about Lot/ Batch number requested.

Other Meds:

Current Illness:

ID: 1305082
Sex: M
Age:
State: VA

Vax Date: 02/01/2021
Onset Date: 02/02/2021
Rec V Date: 05/11/2021
Hospital:

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Symptom List: Vomiting

Symptoms: Fever; Nausea; Vomiting; No appetite; Chills; body ache; Headache; Excessive sweat; Difficulty breathing; Hyperventilation; Exhaustion; This is a spontaneous report from a contactable consumer (patient, reported on himself). A 47-year-old male patient received BNT162B2 (BNT162B2, solution for injection, Batch/Lot Number: EN5318 and expiration date not provided), via an unspecified route of administration in left arm on 01Feb2021 04:30 PM, as a single dose for covid-19 immunization. Medical history included depression, COVID in late Nov2020, she had two tests for COVID which were found to be negative. She was allergic to Fructans. Concomitant medications in two weeks included vortioxetine (Trintellix), esketamine hydrochloride (Spravato), rosuvastatin calcium (Crestor), Saw palmetto (SERENOA REPENS) Saw Palme and Fish Oil. 02Feb2021 Tuesday 09:00 AM, the patient experienced symptoms 85 percent similar in type and intensity to when she had Covid in late Nov2020. Beginning with fever 99-101 until Saturday. She also had nausea and vomiting. She had no appetite (no food Tuesday till Saturday). She experienced chills, body ache, headache, excessive sweat, difficulty breathing, hyperventilation and exhaustion. The patient did not receive treatment for the events. He did not have any other vaccine in four weeks. The patient was not tested for covid tested post vaccination. Vaccine facility type: Public Health Clinic/Administration facility. The outcome of the events was recovering. Information on batch/lot number has been requested.

Other Meds: TRINTELLIX; SPRAVATO; CRESTOR; SAW PALMETTO [SERENOA REPENS]; FISH OIL

Current Illness:

ID: 1305083
Sex: F
Age:
State: OR

Vax Date: 02/05/2021
Onset Date: 02/05/2021
Rec V Date: 05/11/2021
Hospital:

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Symptom List: Headache, Limb discomfort, Nasal congestion

Symptoms: Severe depression and anxiety started about 1 hour post injection and lasted for about 36 hours.; Severe depression and anxiety started about 1 hour post injection and lasted for about 36 hours.; This is a spontaneous report from a contactable Consumer (patient, self-reported). A 29-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not provided), via an unspecified route of administration, in Arm right, on 05Feb2021 at 10:15 AM, as a single dose for COVID-19 immunization. The patient was not pregnant at the time of vaccination. The patient's medical history included anxiety disorder. The patient had known allergies with metformin and fluoxetine. Concomitant medications included bupropion hydrochloride (WELLBUTRIN) (300 mg) and sertraline hydrochloride (ZOLOFT) (50 mg). The patient did not receive any other vaccine in four weeks. The patient was not diagnosed with COVID prior vaccination. The patient was not tested for COVID post vaccination. The patient reported that on 05Feb2021 at 11:00 AM, she had severe depression and anxiety started about 1 hour post injection and lasted for about 36 hours. The patient did not receive any treatment for the events. Outcome of the events was recovering. Information on the lot/ batch number has been requested. Follow-up attempts completed. No further information expected.

Other Meds: WELLBUTRIN; ZOLOFT

Current Illness:

ID: 1305084
Sex: M
Age:
State: CT

Vax Date: 01/26/2021
Onset Date: 02/14/2021
Rec V Date: 05/11/2021
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Symptom List: Back pain, Cold sweat, Headache, Nausea, Vomiting

Symptoms: shingles; This is a spontaneous report from a contactable consumer (patient). A 59-year-old male patient received the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Lot Number: EL3247), via an unspecified route of administration, administered in Arm Left on 26Jan2021 13:30 as single dose for COVID-19 immunization in a workplace clinic. Medical history included arthritis, obesity, and other inflammatory diseases from an unknown date. No known allergies. Concomitant medications included celecoxib (CELEBREX); hydrochlorothiazide, quinapril hydrochloride; and amlodipine all taken for an unspecified indication, start and stop date were not reported. No other vaccines in four weeks. No COVID-19 prior to vaccination. The patient experienced shingles on 14Feb2021 that was diagnosed on 16Feb2021. The patient took antiviral medication to treat shingles. The outcome of the event was recovering. The patient was tested for COVID-19 post vaccination via nasal swab on 27Jan2021 with a negative result. The patient received the second dose of bnt162b2 (Lot number: EL3247) on 16Feb2021 10:15 on the left arm for COVID-19 immunization. The patient reported that "neither my doctor nor I think there is a connection between the vaccine dosed and shingles".; Sender's Comments: The reported shingles was most likely an intercurrent disease, and unlikely related to the first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE).

Other Meds: CELEBREX; QUINAPRIL HCL/HYDROCHLOROTHIAZIDE; AMLODIPINE

Current Illness:

ID: 1305085
Sex: F
Age:
State: NY

Vax Date: 02/14/2021
Onset Date: 02/17/2021
Rec V Date: 05/11/2021
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Symptom List: Injection site swelling, Limb discomfort

Symptoms: shingles; This is a spontaneous report from a contactable consumer (patient). A 52-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 14Feb2021 (Batch/Lot number was not reported) as SINGLE DOSE for covid-19 immunisation, age at vaccination 52 years old. Medical history included breast cancer female on the right side, High cholesterol, Allergic to Sulfa; all from unspecified dates. No concomitant medications. She did not have any new medications, no new soaps, and no new food. She had no other vaccines on the same day or in the 4 weeks prior. The patient experienced shingles on 17Feb2021. The patient woke up having a severe rash that goes from her upper right back to the under the right arm to the right breast. The rash was described as being very red in color, it was all connected, blotchy, and in the rash, there are little bumps like pimples, and it was hot to touch. She had her husband look at her and check her, the rash still looks about the same since this morning. She is concerned because she had breast cancer and read that one side effect lead to lymphoma. The Breast Cancer was on her right side, which is the same side she was having her rash, but the vaccine was administered on the left. She had regular labs yesterday, she gets checked for high cholesterol. They told her everything looked good (16Feb2021). She has not made a visit to the ER. Patient wanted to know if it was okay to get the second dose. She is schedule on 07Mar2021 for the second dose. She had made a Physician Office appointment. Patient thought she was having a reaction to the Pfizer COVID 19 vaccine, but she went to the doctor and they told her she has shingles. The doctor told her to wait to get the 2nd dose until after the shingles goes away, about 6 weeks after the 1st dose. Outcome of the event shingles was unknown. Information about lot/batch has been requested.

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Current Illness:

ID: 1305086
Sex: F
Age:
State: SC

Vax Date: 02/02/2021
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Rec V Date: 05/11/2021
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Symptom List: Chills, Diarrhoea, Fatigue, Feeling abnormal, Headache

Symptoms: Had headache not all the time but every once in a while; Have chills every once in a while; tired; This is a spontaneous report received from a contactable consumer or other non hcp. A 72-years-old female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot/Batch number: EL9265, Pfizer NTEC), via an unspecified route of administration on 02Feb2021 as single dose for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. The reporter stated that she had some reactions and that is not that they were but she concerned about herself and she had headache not all the time but every once in a while, have chills every once in a while and she tired, unusually tired on an unspecified date. Therapeutic measures were taken as a result of Had headache not all the time but every once in a while, Have chills every once in a while and tired and treatment included TYLENOL. The outcome of the events was reported as recovered on an unspecified date.

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Current Illness:

ID: 1305087
Sex: F
Age:
State: IL

Vax Date: 02/17/2021
Onset Date: 02/17/2021
Rec V Date: 05/11/2021
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Symptom List: Hot flush, Myalgia, Nausea, Tension headache

Symptoms: excruciating pain in her arm; can't lift or rotate her arm more than 5 degrees; This is a spontaneous report from a contactable consumer (patient). A 45-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), dose 2 via an unspecified route of administration, administered in arm on 17Feb2021 (lot number: EM9810) as SINGLE DOSE for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient previously took the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL3247) for COVID-19 immunization. On 17Feb2021 17:00, the patient started to feel the symptoms. The patient had an excruciating pain in her arm and can't lift or rotate her arm more than 5 degrees. Therapeutic measures were taken as a result of the events which included treatment with Advil and ice. The outcome of the events was unknown.

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Total 2021 VAERS Injuries: 704,237

Page last modified: 26 October 2021 2:21am