VAERS 2021 Database www.vaers.hhs.gov

Main Page | All 2021 Deaths | Videos
VAERS Updated: 10/01/2021
** VAERS DATABASE Last updated: October 1, 2021**
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Manufacturers

Total Manufacturer

Incidents per State

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

ID: 1486302
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 07/20/2021
Hospital:

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Symptom List:

Symptoms: swollen lymph node; This is a spontaneous report from a lay media report reporting events for 3 patients. This is patient 1 of 3. This is a spontaneous report from a contactable consumer. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection Lot number was not reported), via an unspecified route of administration on an unspecified date as a single dose for COVID-19 immunization. The patient medical history and concomitant medications were not reported. The patient experienced swollen lymph node on an unspecified date. She described one patient with a newly diagnosed breast tumor who had swollen lymph nodes on the same side and had recently received a Covid shot in the arm on that side. A biopsy was performed, an important step to determine whether there were malignant cells in the nodes that would then help decide a course of treatment. It was negative for cancer. The vaccine had most likely caused the swelling. The patient underwent lab tests and procedures which included biopsy: negative for cancer on unspecified date. Outcome of the event was unknown.; Sender's Comments: Linked Report(s) : Same article/same event/different patient

Other Meds:

Current Illness:

ID: 1486303
Sex: F
Age:
State: CA

Vax Date: 06/14/2021
Onset Date: 06/01/2021
Rec V Date: 07/20/2021
Hospital:

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Symptoms: My arm had a rash on it and its swollen. It is always on my arms and my hands. It went up to my throat so, and sick right away after I have this. I mean had really awful for three days.; My arm had a rash on it and its swollen. It is always on my arms and my hands. It went up to my throat so, and sick right away after I have this. I mean had really awful for three days.; My arm had a rash on it and its swollen. It is always on my arms and my hands. It went up to my throat so, and sick right away after I have this. I mean had really awful for three days.; My arm had a rash on it and its swollen. It is always on my arms and my hands. It went up to my throat so, and sick right away after I have this. I mean had really awful for three days.; I had a bad reaction because of any other medication consider allergic to it.; This is a spontaneous report received from a contactable consumer (patient). A 61-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/lot number was not reported) via intramuscular route of administration in Arm Left on 14Jun2021 as single dose for covid-19 immunization. Medical history included blood pressure from an unknown date and unknown if ongoing. Concomitant medication included propanol taken for hypertension, start and stop date were not reported. In Jun2021 patient had her 1st shot of vaccine, 3 weeks ago and just, had a, she thinks, a had a bad reaction because of any other medication consider allergic to it. Her arm had a rash on it and its swollen. It was always on her arms and hands. It went up to her throat so, and she was sick right away after she had this. She had really awful three days after she had the shot. This does not mean that she was having allergic reaction, she stated. She stated she should not get the second shot. Patient stated it started hours after the shot. The person actually right away, I don't know it was the vaccine necessarily or the person giving me the shot but I am wondering if he or his arm, start turning black and blue. She doesn't have the vaccination card. 13Jun, 14Jun I guess she confirmed as 14Jun2021. Consumer stated, her second shot is due. The LOT number for the first dose, this, she can tell this person had very bad handwriting. It's look like EW0101. Treatment taken for Adverse Event with Benadryl, Diphenhydramine 50 mg, Norco 10/325 mg. Therapeutic measures were taken as a result of the events. The clinical outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds: PROPANOL

Current Illness:

ID: 1486304
Sex: M
Age:
State: NJ

Vax Date: 07/02/2021
Onset Date: 07/02/2021
Rec V Date: 07/20/2021
Hospital:

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Symptoms: Violently Sick; Throwing up/ Violent vomiting to Biel for 6 hours straight; cannot drink fluids or foods for 12 hours plus.; Chills; Joint pain; barely able to move or walk; Fever/Fevor 101; barely able to move or walk; Muscle pain; Nausea; Feeling unwell; Injection site pain; Tiredness; arm pain; Headache; injection site redness; injection site redness & swelling; He has minor discomfort; Diarrhea; This is a spontaneous report from a contactable consumer (patient). A 62-year-old male patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection, Batch/Lot Number: EW0180), via an unspecified route of administration, administered in arm left on 02Jul2021 at 10:30 AM (at the age of 62-year-old) as dose 2, single for COVID-19 immunization. Medical history included valtrex for infection in right eye, known allergies: mold, mildew, blue grass, dust, mites, cockroaches (start - 10 to 15 years). The patient concomitant medication included valaciclovir hydrochloride (VALTREX), allergy shots taken for allergy (patient stated it changes based on vials). Patient did not receive any other vaccine within 4 weeks prior vaccinations. Patient was not diagnosed with COVID prior vaccination. Patient was not tested COVID post vaccination. The patient previously took first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for Injection, Batch/Lot Number: EN6200), via an unspecified route of administration, administered in arm right on 02Jul2021 at 05:45 PM (at the age of 62-year-old) as dose 1, single for COVID-19 immunization. The patient experienced he has minor discomfort, diarrhea on an unspecified date in 2021; injection site pain (the date patient received the vaccine), tiredness, arm pain, feeling unwell (subsided from feeling violently sick yesterday), headache, injection site redness, injection site redness & swelling on 02Jul2021; nausea on 04Jul2021; violently sick (It started at 5am (67 to 68 hours after vaccination). It has mostly subsided, gone away. Patient stated he has recovered with lasting effects because he was so beat up from throwing up) on 05Jul2021 at 05:00 AM, throwing up/ violent vomiting to biel for 6 hours straight (at 5 or 6 am yesterday. It lasted around 6 hours until noon), cannot drink fluids or foods for 12 hours plus, chills (around 5 or 6 am), joint pain (5 to 6 am), barely able to move or walk, fever/fever 101 (5 to 6 am, patient temperatures are normal now), muscle pain (around 5 or 6 am) on 05Jul2021. Adverse events did not result in emergency room, physician office visit. Adverse event: 12 of the 17 listed side effects on fact sheet revised 10May2021. injection site redness and swelling, arm pain. Feeling unwell, off. Joint and muscle pain, barely able to move or walk. Chills & Fevor 101. Violent vomiting to bile for 6 hours straight. cannot drink fluids or foods for 12 hours plus. Patient is calling about the vaccine, stated covid 19. He got the vaccine, his second shot and had a reaction that is on the paperwork. The patient underwent lab tests and procedures which included fever was 101 on 05Jul2021. The patient received tylenol, advil and pepto-bismol as treatment medication for the events joint pain, nausea, headache, fever/fever 101, muscle pain. Outcome of the events violently sick, feeling unwell, he has minor discomfort, diarrhea was unknown; tiredness, arm pain, cannot drink fluids or foods for 12 hours plus, joint pain, headache, injection site redness, muscle pain was recovering; injection site pain, throwing up/ violent vomiting to bile for 6 hours straight was recovered on 05Jul2021; chills, barely able to move or walk, nausea, injection site redness & swelling, fever/fever 101 was recovered on 06Jul2021. Follow-up (PRD/SRD 08Jul2021): Follow-up attempts are completed. No further information is expected.

Other Meds: VALTREX

Current Illness:

ID: 1486305
Sex: F
Age:
State: CO

Vax Date:
Onset Date:
Rec V Date: 07/20/2021
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Symptoms: "She had a shingles vaccine on 05/28/21; This is a spontaneous report from a Pfizer- sponsored program XELSOURCE. A contactable other HCP (nurse) reported that. A 67-years-old female patient received bnt162b2 (Pfizer-BioNTech COVID-19 Vaccine, Solution for injection), dose 1 via an unspecified route of administration on an unspecified date (age at vaccination 67-years) (Batch/Lot number was not reported) as DOSE 1, SINGLE for covid-19 immunisation; tofacitinib citrate (XELJANZ, 5 mg tablets), route of administration, start and stop date, batch/lot number and dose were not reported for an unspecified indication. The patient medical history and concomitant medications were not reported. Nurse stated, She had a shingles vaccine on 28May21. She would have a second vaccine done after July 28 up to September. The action taken in response to the events for xeljanz was unknown. . The outcome of event was unknown.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021846249 same reporter/patient/drug, diffent event/dose

Other Meds:

Current Illness:

ID: 1486306
Sex: M
Age:
State: NC

Vax Date: 03/30/2021
Onset Date: 04/19/2021
Rec V Date: 07/20/2021
Hospital: Y

Vax Type:
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Symptoms: Congestive Heart FailureFluid Buildup in lungsEnlarged HeartPalpitation in beating of heart; Congestive Heart FailureFluid Buildup in lungsEnlarged HeartPalpitation in beating of heart; Congestive Heart FailureFluid Buildup in lungsEnlarged HeartPalpitation in beating of heart; Congestive Heart FailureFluid Buildup in lungsEnlarged HeartPalpitation in beating of heart; This is a spontaneous report from a contactable consumer (patient). A 62-years-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 MRNA VACCINE, Solution for injection, Lot Number: ER8734, expiry date not reported), via an unspecified route of administration, administered in right arm on 30Mar2021 09:30 (at the age of 62 years old) as dose 2, single for covid-19 immunization. The patient's medical history was not reported. Prior to vaccination, the patient was not diagnosed with COVID-19. There were no concomitant medications. The most recent COVID-19 vaccine was administered in the doctor's office/urgent care. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient did not receive any other medications within 2 weeks of vaccination. Patient received the first dose of BNT162B2 (lot number EN6206) as Covid-19 immunization on 09Mar2021 9:30 am (at the age of 62 years old) administered in the right arm. On 19Apr2021 21:00, the patient experienced congestive heart failure, fluid buildup in lungs, enlarged heart, and palpitation in beating of heart. The events were reported as serious, hospitalization on unknown dates for 4 days, disability, and were life threatening. Adverse events resulted in doctor or other healthcare professional office/clinic visit, and emergency room/department or urgent care. Therapeutic measures were taken in response to the events which included unspecified medicines. Since the vaccination, the patient has not been tested for COVID-19. The outcome of the events reported was not recovered.

Other Meds:

Current Illness:

ID: 1486307
Sex: M
Age:
State:

Vax Date: 04/13/2021
Onset Date: 04/01/2021
Rec V Date: 07/20/2021
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Symptoms: Received the first dose oft he Pfizer Covid vaccine on 13 Apr 2021. He then tested positive for Covid-19; Received the first dose oft he Pfizer Covid vaccine on 13 Apr 2021. He then tested positive for Covid-19; This is a spontaneous report from a contactable pharmacist from a Pfizer sponsored program. A 42-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on 13Apr2021 as dose 1,single for COVID-19 immunization. The patient medical history and concomitant medications were not reported. Reported as, patient who received the first dose of the Pfizer Covid vaccine on 13Apr2021. He then tested positive for Covid-19. Received 1st Pfizer Covid 19 vaccine on 13Apr and tested positive the end of Apr2021. Reporter would like to know when consumer can receive 2nd Pfizer Covid vaccine. The patient underwent lab tests and procedures which included sars-cov-2 test positive: positive on an unspecified date on Apr2021. Outcome of the events were unknown. Information on the lot/batch number has been requested.; Sender's Comments: As there is limited information in the case provided, the causal association between the events of COVID-19 and Drug ineffective and the suspect product BNT162B2 cannot be excluded. The case will be reassessed once new information is available.

Other Meds:

Current Illness:

ID: 1486308
Sex: F
Age:
State: GA

Vax Date:
Onset Date: 06/14/2021
Rec V Date: 07/20/2021
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Symptoms: diagnosed with COVID monday, 14Jun2021 after completing Pfizer vaccine series.; diagnosed with COVID monday, 14Jun2021 after completing Pfizer vaccine series.; This is a spontaneous report from a contactable consumer (patient). A female patient of an unspecified age received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as single dose and received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Batch/Lot number was not reported) via an unspecified route of administration on an unspecified date as single dose for COVID-19 immunisation. The patient medical history and concomitant medications were not reported. On 14Jun2021, the patient experienced diagnosed with COVID Monday, 14Jun2021 after completing Pfizer vaccine series. On unspecified date, voice was raspy, she said she felt very tired. But hope to return to work on Wednesday (unspecified date). The patient underwent lab tests and procedures which included COVID-19: positive on 14Jun2021. The clinical outcome of events was unknown. Information on Lot/Batch number has been requested.

Other Meds:

Current Illness:

ID: 1486309
Sex: M
Age:
State: GA

Vax Date: 04/20/2021
Onset Date: 05/30/2021
Rec V Date: 07/20/2021
Hospital: Y

Vax Type:
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Symptoms: chest pain; uncomfortable; This is a spontaneous report from a contactable consumer (patient). A 49-years-old male patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number: EW0162; Expiration Date: 31Jul2021) via an unspecified route of administration, administered in left upper arm on 20Apr2021 09:30 as dose 1, single and dose 2 via an unspecified route of administration, administered in arm left on 19May2021 09:30 (Batch/Lot Number: EW0183; Expiration Date: 31Aug2021) (at the age of 49-years-old) as dose 2, single for COVID-19 immunization (He discussed it with his 21 year old daughter and wife). Caller wanted to get back and do some things. He felt that if he got Covid after the vaccine, he would not get as many side effects. He did get his flu shot and the experience had always been positive. His daughter also got flu shot and had positive experience. Caller thought that most people who didn't get shots was because they were afraid of needles. He thought maybe there was a different way to administer it so more people were taking it. Medical history included ongoing hypertension (About 14 years). He did not have high blood pressure if he was exercising. It was in good control. When caller was asked if he had a family history related to reactions to any vaccines, he stated that both his mother and father got the vaccinations. They were the first ones in the elderly group. His dad got sick and got a little lethargic and out of it for a day or so. He was not feeling well. His Mom just had a sore arm. Caller declined to do report on his parents. Concomitant medication included olmesartan medoxomil (BENICAR) taken for hypertension from an unspecified start date and ongoing, he said he really didn't needed to take it anymore, but he still took it and had been taking it for about 14 years. The patient experienced chest pain on 30May2021 around 22:00 and was uncomfortable on an unspecified date with outcome of unknown. Caller stated his first dose was on 20Apr2021 and his second dose was 19May2021. Caller stated on 30May he started having chest pain, so he went to the ER and was at the hospital for a day and a half for observation. Caller stated he now had a cardiologist appointment on 05Aug2021 and even though all of the tests came back negative, they put him on low dose aspirin. Caller stated he had seen the studies about 19-39-year-olds having chest pain and inflamed hearts and would like to know if there was information based on his age. Caller asked if there was anything he could do or take for the chest pain. Caller stated that it had been going on for a while and he was very uncomfortable. Stated that Pfizer cannot make treatment recommendations. Stated that caller got both doses of the Pfizer Covid vaccine. He experienced lots of chest pain. It was a dull achy pain near his heart in his chest. It occurred a week later after his second shot. Caller wanted to know if Pfizer offered assistance. He said that he was going to accrue a great deal of expenses. He had an appointment with a cardiologist on 05Aug2021. His appointment was so far out as that was what he could schedule. Caller also said that he was at the ER for a day and a half as they wanted to remove all life threatening possibilities such as the risk of a heart attack. They could not find a heart attack. He's never had a heart attack, but from what people described to him, that feeling in his chest.ck. When caller was asked if he was a healthcare provider, he said that he had done First aid, but he was not a healthcare provider. Caller did not want to provide email address. Caller clarifies that he had chest pain on Sunday night, around 22:00. He was sitting on his couch watching TV. Outcome: States it is persisting, then states he felt that there was a slight improvement at this time. He did not feel it around the clock like he did the first week when it was constant pain. It was coming and going very frequently. Caller stated that the only thing they told him to do was take a baby Aspirin 81mg. They told him he could resume activities. He walked and hiked a lot. He was hesitant to hike with altitude. He did outdoor activities like cutting the grass. There was no difference in the feeling of the chest pain whether he was doing activity or resting. It didn't make it better or worse. Caller stated that they did several tests on his heart when he was at the ER. His heart was strong. They could not find anything. They wanted him to go to the cardiologist to get an EKG and sonogram. He would have those done 05Aug2021 before his meeting with the cardiologist. His blood pressure in the ER when he arrived was 133/89 approximately. It lowered as they kept taking it. Caller stated that he knew probably 10 to 15 black males who took shot. None of them had this problem. They had normal side effects such as sore arm and lethargic feeling after the second dose. He was talking to them to see if anyone had anything like this. None of them had chest pain. Some of them were big men like 270 to 280 pounds. Caller declined to do reports on these men. No further information provided. It was a park that had everything there. He had to schedule the appointment. It was a very legitimate site. Caller provided the address as (address withheld). When caller was asked if he had any adverse reactions to any other shots, he said he had the flu shot and was fine. He had been getting that done forever and he had a sore arm only. Caller stated that the purpose of his call was two-fold. First, he wanted to know about assistance with his expenses. Second he wanted to provide information. He did not know about inflammation in the heart. He heard about CDC report of inflammation in the heart in age group 18 to 39 but not in his age group. Blood pressure of patient was 133/89 approximately. The outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds: BENICAR

Current Illness: Hypertension (About 14 years)

ID: 1486310
Sex: F
Age:
State: CA

Vax Date:
Onset Date:
Rec V Date: 07/20/2021
Hospital:

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Symptoms: The caller reports she tested positive for Covid illness about a week ago, and she then passed it on to her daughter; The caller reports she tested positive for Covid illness about a week ago, and she then passed it on to her daughter; This is a spontaneous report from a contactable consumer. This consumer reported for a 53-year-old female patient (reporter's daughter). A 53-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as dose 2, single and Dose 1, single on an unspecified date for covid-19 immunization. The patient medical history and concomitant medications was not reported. The caller was a consumer who reported that she is 74-year-old female and her daughter 53-year-old had both been fully vaccinated with the Pfizer-Biontech COVID-19 vaccine. The caller reported she tested positive for Covid illness about a week ago (on an unspecified date), and she then passed it on to her daughter (on an unspecified date). She indicated that they had followed CDC recommendations that stated fully vaccinated patients can be around each other and need not wear a mask. She asked for how many people in the population who were fully vaccinated had tested positive for Covid19, the percentages, and the percent of the cases which were the new delta variant. The patient underwent lab tests and procedures which included sars-cov-2 test positive: positive on an unspecified date. Outcome of the events was reported as Unknown. No follow up attempts are needed. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021846613 same reporter/drug/event, different patient

Other Meds:

Current Illness:

ID: 1486311
Sex: F
Age:
State: UT

Vax Date: 03/30/2021
Onset Date: 06/22/2021
Rec V Date: 07/20/2021
Hospital: Y

Vax Type:
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Lot:
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Lab Data:

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Symptom List:

Symptoms: Blood clots both lungs; This is a spontaneous report from a contactable consumer (patient). A 67-year-old female patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number: not reported) via an unspecified route of administration, administered in right arm on 30Mar2021 12:00, as DOSE 2, SINGLE for COVID-19 immunisation in pharmacy. Medical history included sulphate drugs allergy. The patient's concomitant medications were not reported. Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Since the vaccination, the patient had not been tested for COVID-19. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, lot number: not reported), administered in right arm on 09Mar2021 02:00, as DOSE 1, SINGLE for COVID-19 immunisation. On 22Jun2021, the patient had blood clots both lungs. The event reported as serious. The event resulted in doctor or other healthcare professional office/clinic visit and emergency room/department or urgent care hospitalization. Therapeutic measures were taken as a result of blood clots both lungs and treatment with heparin. Outcome of the event was not resolved. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1486312
Sex: F
Age:
State: FL

Vax Date: 06/30/2021
Onset Date: 07/02/2021
Rec V Date: 07/20/2021
Hospital:

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Symptoms: Covid 19 contagion. Muscle aches, fever, sore throat, cough; This is a spontaneous report from contactable consumer (patient, self-reported). A 22-years-old female patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EW0186 and expiry date was not reported), via an unspecified route of administration, in Arm Left, on 30Jun2021 at 14:30 PM (age at vaccination: 22 years), as a single dose for COVID-19 immunization at Pharmacy or Drug store. The patient was not pregnant at the time of vaccination. The patient's medical history and concomitant medications were not reported. The patient did not have any known allergies. 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 was tested for COVID-19. The patient reported that on 02Jul2021 at 23:30 PM, she experienced Covid 19 contagion. muscle aches, fever, sore throat, cough. The patient underwent lab tests and procedures which included sars-cov-2 test: negative on 03Jul2021 and sars-cov-2 test: positive on 05Jul2021. The patient received treatment for the event. Outcome of the event was recovering. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1486313
Sex: M
Age:
State: OR

Vax Date: 05/03/2021
Onset Date: 05/17/2021
Rec V Date: 07/20/2021
Hospital:

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Symptoms: Developed noticeable DVT in the right leg with left leg also having a clot.; Developed noticeable DVT in the right leg with left leg also having a clot.; This is a spontaneous report from a contactable consumer (patient) reported for himself. A 52-years-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EW0168, Expiration Date: Aug2021) via an unspecified route of administration, administered in left arm on 03May2021 (age at vaccination was 52 years) as dose 2, single for COVID-19 immunization. The patient did not have any relevant medical history and concurrent conditions. The patient did not receive any other medications within 2 weeks of vaccination. The patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number: EP7533, Expiration Date: Jul2021) via an unspecified route of administration, administered in left arm on 05Apr2021 at 16:00 pm (age at vaccination was 52 years) as dose 1, single for COVID-19 immunization. The patient previously took Sulfa drugs and experienced known allergies to it. The facility where the most recent COVID-19 vaccine was administered was Pharmacy or Drug Store. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 17May2021, the patient developed noticeable DVT in the right leg with left leg also having a clot. The adverse events resulted in Doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. The patient received treatment with blood thinners for the adverse events. The device date was reported as 06Jul2021. The events were reported as serious (disabling/Incapacitating). The outcome of the events at the time of last observation was not resolved. Follow-up actions are completed. Further information has been requested.

Other Meds:

Current Illness:

ID: 1486314
Sex: M
Age:
State: FL

Vax Date:
Onset Date:
Rec V Date: 07/20/2021
Hospital:

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Symptoms: Tested positive; Tested positive; This is a spontaneous report from a contactable consumer (patient). A male patient of an unspecified age received first and second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) as DOSE 1, SINGLE and as DOSE 2, SINGLE for covid-19 immunization. The patient medical history and concomitant medications were not reported. The patient stated I am vaccinated with the 2 doses against COVID-19 and I and my wife tested positive. The patient underwent lab test and procedure which included: SARS-CoV-2 test which was positive on an unspecified date. The outcome of the events was unknown. Information about lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1486315
Sex: M
Age:
State: FL

Vax Date: 06/11/2021
Onset Date: 06/22/2021
Rec V Date: 07/20/2021
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Symptoms: On Friday I was dianogosed with Bell's Palsy.; On Thursday night i started showing signs of a full-blown stroke; June 22nd I started having issues with my eye. It would look like it was cloudly and I couldn't blink.; June 22nd I started having issues with my eye. It would look like it was cloudly and I couldn't blink.; This is a spontaneous report from a contactable consumer or other non hcp(patient). A 34-years-old male patient received bnt162b2 (Pfizer covid vaccine, formulation: solution for injection, tch/Lot Number: EW0185), via an unspecified route of administration, administered in Arm Right on 11Jun2021 12:00 (at the of 34-years-old) as DOSE 2, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. Prior to the vaccination the patient was not diagnosed with covid. The patient had no allergies. Since the vaccination, the patient had not been tested for covid 19. The patient previously took BNT162B2(Pfizer covid vaccine, formulation: solution for injection, lot number=EW0168) via unspecified route of administration, administered in Arm right on 19May2021 12:00 as DOSE1, SINGLE for covid 19 immunisation. On 22Jun2021 at 19:00, the patient experienced having issues with his eye. It would look like it was cloudly and he could not blink and eye disorder. On 23Jun2021 , Wednesday, the patient experienced issue with his eye and got worse. On 24Jun2021 Thursday night, the patient started showing signs of a full-blown stroke. On 25Jun2021 Friday, patient was diagnosed with bell's palsy and on Wednesday the issue with eye got worse. The outcome of the events was not recovered. Follow-Up (09Jul2021): Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1486316
Sex: M
Age:
State: FL

Vax Date: 05/18/2021
Onset Date: 05/22/2021
Rec V Date: 07/20/2021
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Symptoms: he developed multisystem inflammatory syndrome; Big spleen; This is a spontaneous report from a contactable consumer (patient's parent) via a Pfizer-sponsored program. A male patient (age not provided) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Lot number not provided), via an unspecified route of administration, on 18May2021 at single dose for COVID-19 immunisation. No relevant medical history and concomitant medications were provided. On 22May2021, the patient developed multisystem inflammatory syndrome and big spleen. The outcome of the events was unknown. Information about Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 1486317
Sex: U
Age:
State: MO

Vax Date: 04/09/2021
Onset Date: 07/05/2021
Rec V Date: 07/20/2021
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Symptoms: covid test was positive after both doses; covid test was positive after both doses; This is a spontaneous report from a contactable consumer (patient). A patient of unspecified age and gender received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot number: EP7534) via an unspecified route of administration on 19Mar2021 as dose 1, single; and later received second dose of BNT162B2 (Lot number: ER8734) on 09Apr2021 as dose 2, single; both for covid-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that patient received the two parts of Pfizer vaccine on 19Mar2021 and 09Apr2021 and experienced a week of symptoms, losing taste and smell was the clincher in Jun2021. After that patient went to a local urgent care and had a nasal swab covid test that was positive on 05Jul2021. Patient was told that many vaccinated people were testing positive in his/her area. On 05Jul2021, the patient underwent lab tests and procedures which included sars-cov-2 test which result was positive. The outcome of the events was unknown. Follow-up attempts are completed. No further information is expected.

Other Meds:

Current Illness:

ID: 1486318
Sex: F
Age:
State: CA

Vax Date: 03/04/2021
Onset Date: 04/10/2021
Rec V Date: 07/20/2021
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Symptoms: I am worried that the vaccine has messed up my immune system and caused my RA to come back; I am worried that the vaccine has messed up my immune system; My fingers started swelling; The pain and swelling in my hands is now excruciating and it is starting in my feet; My fingers are starting to twist and curl; This is a spontaneous report from a contactable consumer or other non hcp (patient, self-reporting). A 57-year-old non pregnant female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Batch/Lot Number: EN6203 and expiration date was not reported), via an unspecified route of administration in arm left on 04Mar2021 at 12:30 as dose 2, single (age at vaccination 57-year-old) for COVID-19 immunisation. Medical history included rheumatoid arthritis from an unknown date, Thyroid Disease from an unknown, Hashimotos from an unknown date. The patient previously took levaquin and experienced hypersensitivity. Historical vaccine information included first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, lot number EL9261), via an unspecified route of administration in arm left on 12Feb2021 at 12:15 PM for COVID-19 Immunization. Prior to 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 received other medications within 2 weeks of vaccination includes compounded Thyroid med, compounded est/test cream. The patient reported that worried that the vaccine has messed up her immune system and caused RA to come back, her fingers started swelling, the pain and swelling in her hands was now excruciating and it was starting in her feet, her fingers were starting to twist and curl on 10Apr2021. Patient had RA in the past but had been in remission for over a year and a half. About a month after getting the 2nd COVID vaccination her fingers started swelling and hurting. The pain and swelling in her hands was excruciating and it was starting in her feet. Her fingers were starting to twist and curl. She was worried that the vaccine has messed up her immune system and caused her RA to come back way worse than it ever was. This was coming on fast and very severe. She won't be able to work much longer if something wasn't done to reverse the pain and damage. The patient underwent lab tests and procedures which included x-ray: unknown on an unknown date. Therapeutic measures were taken as a result of events includes medication for the pain and inflammation, x rays. The outcome of the events were not resolved. Follow-up actions are needed. Further information has been requested.

Other Meds:

Current Illness:

ID: 1486320
Sex: F
Age:
State: GA

Vax Date:
Onset Date: 06/01/2021
Rec V Date: 07/20/2021
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Symptoms: developed pneumonia 12 days ago; This is a spontaneous report from a contactable consumer (patient). This 60-year-old female patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Lot number not provided), via an unspecified route of administration, on unknown date at single dose for COVID-19 immunisation. No relevant medical history and concomitant medications were provided. In Jun2021 (12 days ago, as reported), the patient developed pneumonia for which he took antibiotics. The outcome of the event was unknown. Information about Batch/Lot number has been requested.

Other Meds:

Current Illness:

ID: 1486321
Sex: M
Age:
State: MI

Vax Date:
Onset Date:
Rec V Date: 07/20/2021
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Symptoms: stroke; This is a spontaneous report from a contactable other hcp. The other hcp reported for both the husband and wife, this is the case for husband. A male patient of an unspecified age received bnt162b2 (COVID-19 VACCINE - MANUFACTURER UNKNOWN), via an unspecified route of administration on unspecified date (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced stroke on unspecified date. Information about batch/lot number has been requested.; Sender's Comments: Linked Report(s) : US-PFIZER INC-2021856673 Same reporter/ drug/event, different patients

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Date Died:

ID: 1486322
Sex: F
Age:
State: MI

Vax Date:
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Rec V Date: 07/20/2021
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Symptoms: stroke; This is a spontaneous report from a contactable other hcp. The other hcp reported for both the husband and wife, this is the case for wife. A female patient of an unspecified age received bnt162b2 (COVID-19 VACCINE - MANUFACTURER UNKNOWN), via an unspecified route of administration on unspecified date (Batch/Lot number was not reported) as single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient experienced stroke on unspecified date and died. It was not reported if an autopsy was performed. Information about batch/lot number has been requested.; Sender's Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the event Cerebrovascular accident and the suspect drug bnt162b2. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.,Linked Report(s) : US-PFIZER INC-2021856461 Same reporter/ drug/event, different patients; Reported Cause(s) of Death: stroke

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Current Illness:

ID: 1486323
Sex: F
Age:
State: NY

Vax Date: 05/18/2021
Onset Date: 05/01/2021
Rec V Date: 07/20/2021
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Symptoms: to notice a set bruises on her left arm(injection site) a few days after the first dose; she is not healing as fast as she used to; This is a spontaneous report from a contactable consumer (patient). A 67-year-old female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; Lot number: EW0182; expiration date: 31Aug2021), via an unspecified route of administration in the left arm on 18May2021 (at the age of 67-year-old) as single dose for COVID-19 immunization. Patient had no medical history. Patient did not receive any other products (no concomitant medication). On an unspecified date in May2021, few days after the first dose of vaccination, patient started to notice a set bruises on her left arm (injection site). Patient reported that, "instead of a couple of days, it's taken longer or about 3 weeks to heal" and was not healing as fast as she used to on an unspecified date in May2021. Patient noticed this up to 3-4 weeks to the first shot. Patient had been rough housing with her grand-children, and the bruises are not disappearing as fast as before, like up to 2-3 weeks before the shot. It was taking her longer to heal. Patient looks like an abused woman right now. She used to work at Pfizer. She keeps seeing more and more of the bruising. Patient clarified that she first noticed it a couple of days after the first shot happened. It took her bruises about 3 weeks to disappear. She then was rough housing with her grandchild again, and she had black and blues on her arms again. This recurs because of something. The bruises are not popping up on their own. Usually if she has a bruise, they go away in 3 days or so. This was like multiplying it by 7. Patient received her second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; Lot number: EW0183; expiration date: 31Aug2021) in left arm on 08Jun2021 as single dose for COVID-19 immunization. Patient was wondering if this was because the vaccine was traveling through her system and asked if there has been reports of this as a side effect and how long will this side effect last. Outcome of both the events were not resolved.

Other Meds:

Current Illness:

ID: 1486324
Sex: F
Age:
State: DC

Vax Date: 04/11/2021
Onset Date: 06/27/2021
Rec V Date: 07/20/2021
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Symptoms: Acute Ischemic stroke caused by blood clot.; Acute Ischemic stroke caused by blood clot.; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 66-year-old non-pregnant female patient received bnt162b2 dose 2 via an unspecified route of administration, administered in Arm Right on 11Apr2021 (Batch/Lot Number: ER8730) as single dose for covid-19 immunisation at the age of 66-year-old. The patient medical history and concomitant medications were not reported. The patient previously took bnt162b2 dose 1 administered in Arm Right on 21Mar2021 (Batch/Lot Number: EP6958) as single dose at the age of 66-year-old. On 27Jun2021, the patient experienced acute Ischemic stroke caused by blood clot. The event resulted in doctor or other healthcare professional office/clinic visit. Treatment received for the event and the patient was still under medical care. The event was reported as serious with seriousness criteria of life threatening. The outcome of the event was unknown. The patient was not diagnosed with COVID-19 prior to vaccination and hasn't been tested for COVID-19 since the vaccination.

Other Meds:

Current Illness:

ID: 1486325
Sex: M
Age:
State: NY

Vax Date: 06/30/2021
Onset Date: 07/01/2021
Rec V Date: 07/20/2021
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Symptoms: My son woke up on thursday 01Jul2021 the day after he received the 2nd dose of the covid 19 vaccine with partial facial paralysis and was diagnosed with bells palsy; My son woke up on thursday 01Jul2021 the day after he received the 2nd dose of the covid 19 vaccine with partial facial paralysis and was diagnosed with bells palsy; This is a spontaneous report from a contactable consumer or other non hcp. A 14-year-old male patient received second dose of BNT162b2 (CONMINTARY, Solution for injection, Lot No: EW0196), via an unspecified route of administration, administered in Arm Left on 30Jun2021 17:45 (at the age of 14-year-old), as 2nd dose single for COVID-19 immunization (Administered at Pharmacy or Drug Store). The patient's medical history and concomitant medications were not reported. Historical vaccine included first dose of BNT162B2(CONMINTARY, Solution for injection, Lot No: EW0191), via Left arm on 23May2021, 01:00 PM (at the age of 14-year-old), for 1st dose, single for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient had no known allergies. No other medical history was reported. Patient did not receive any other medications within 2 weeks of vaccination. Prior to vaccination, patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The reporter stated that their son woke up on Thursday 01Jul2021 the day after he received the 2nd dose of the covid 19 vaccine with partial facial paralysis and was diagnosed with bell's palsy. Events resulted in Doctor or other healthcare professional office/clinic visit and Emergency room/department or urgent care. Therapeutic measures were taken as a result of facial paralysis and bell's palsy. Treatment received included prednisolone. No seriousness criteria was reported. Outcome of the events was not recovered at the time of reporting. Device Date was 09Jul2021. No follow-up attempts needed. No further information expected.

Other Meds:

Current Illness:

ID: 1486326
Sex: F
Age:
State: TX

Vax Date: 01/10/2021
Onset Date: 01/12/2021
Rec V Date: 07/20/2021
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Symptoms: very sore arm; 48 hr after injection developed PVC's - in/out of geminy for 3 days; generalized fatigue which worsened over time with worsening of pvc frequency; Shingles-type nerve pain left trunk; Shingles-type nerve pain left trunk; eruption of herpes in corner of mouth; scalp pain; unifocal pvc's at first, which slowly progressed into more frequent and multifocal pvc's , worsening with any increased activity; unifocal pvc's at first, which slowly progressed into more frequent and multifocal pvc's , worsening with any increased activity; This is a spontaneous report from a contactable Nurse (Patient). A 57yearsold female patient received bnt162b2 (PFIZER BIONTECH COVID19 VACCINE, solution for injection, Lot Number: EL3302, at age of vaccination 57 years), dose 2 via an unspecified route of administration, administered in Arm Left on 10Jan2021 15:00 as dose 2, single for covid19 immunisation. Medical history included Hypothyroidism and allergies (Mild latex, mild food allergies associated with latex). Concomitant medication(s) included levothyroxine, thyroid (ARMOUR THYROID), asa, colecalciferol (VITAMIN D), ascorbic acid, betacarotene, cupric oxide, manganese sulfate, selenium, tocopheryl acetate, ubidecarenone, zinc oxide (COQ10). Previously patient received bnt162b2 (BNT162B2, solution for injection), dose 1 via an unspecified route of administration, administered in Arm Left on 18Dec2020 10:00 AM (Batch/Lot Number: ELO140) as dose 1, single for covid19 immunisation. From first injection patient experienced sore arm for few hrs, fatigued 2 days, felt cold (wore jacket) and x2days (afebrile). The patient did not receive any other vaccine in fourweeks. It was unknown if patient had covid prior vaccination. Patient did not test covid post vaccination. On 12Jan2021at 01:00 PM, the patient experienced very sore arm x 3 days, 48 hr after injection developed PVCs in/out of geminy for 3 days then geminy resolved but remained with what seemed like unifocal pvcs at first, which slowly progressed into more frequent and multifocal pvcs , worsening with any increased activity (ex: walking from parking lot to work place), generalized fatigue which worsened over time with worsening of pvc frequency. Lasted almost exactly 4 months from day of injection (15 weeks). About to request cardiology referral, increased ASA intake to 350 mg bid (was 81 mg qd) (selfprescribed) and pvcs progressively resolved over 4, 5day period then stopped completely. Energy returned. Also, developed scalp pain (abt 10 d, resolved then returned), then developed Shinglestype nerve pain left trunk, and also 2x over that 4 mo. had neareruption of herpes in corner of mouth (in remission x40 yrs). Patient received treatment for the event extrasystoles, and no treatment was taken for other events. The outcome of event scalp pain was recovered with Sequel.The outcome of event very sore arm, 48 hr after injection developed PVCs in/out of geminy for 3 days, unifocal pvcs at first, which slowly progressed into more frequent and multifocal pvcs , worsening with any increased activity was recovered on 15Jan2021. The outcome of the events all others was recovered on unspecified date 2021. No followup attempts are possible. No further information is expected

Other Meds: LEVOTHYROXINE; ARMOUR THYROID; ASA; VITAMIN D; COQ10

Current Illness:

ID: 1486327
Sex: U
Age:
State:

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Rec V Date: 07/20/2021
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Symptoms: My heart was like killing me; heart still hurts and I never had problem with my heart; Flu like symptoms; Severe muscle ache; Joint ache; This is a spontaneous report from a contactable consumer or other non hcp. A patient of unspecified age and gender received second dose of bnt162b2 (Pfizer BioNTech Covid 19 vaccine, formulation: solution for injection, Batch/Lot Number: ER8734) via an unspecified route of administration on an unspecified date as a single dose for covid-19 immunisation. The patient medical history and concomitant medications was not reported.The patient previously received first dose of bnt162b2 (Pfizer BioNTech Covid 19 vaccine, formulation: solution for injection, Batch/Lot Number: EN6202) via unspecified route of administration on an unspecified date as a single dose for covid-19 immunisation. It was reported the patient was little freaked out, received second dose Pfizer (Covid) vaccine and 12 hours after started having flu like symptoms, severe muscle ache, joint ache and muscle ache and like heart was killing him like. Patient did not know whether need to go to Emergency room or not. Patient was healthy individual, and only go to the Doctor once a year and if it was just a side effect and he will be ok but, heart still hurts. Do patient need to go see a cardiologist. The patient never had problem with his/her heart. The patient was not recovered from heart was like killing me; heart still hurts and unknown for the flu like symptoms, severe muscle ache, joint ache. Follow-up attempt are not possible. No expected further information.

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Current Illness:

ID: 1486328
Sex: M
Age:
State: NY

Vax Date: 06/01/2021
Onset Date: 07/01/2021
Rec V Date: 07/20/2021
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Symptoms: Diarrhoea; Vomiting; This is a spontaneous report from a contactable consumer (Patient). A 25-year-old male patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection; Batch/Lot number was not reported), via an unspecified route of administration, administered in Arm Left on an unspecified date (Saturday) in Jun2021 (at the age of 25-year-old), as DOSE 1, SINGLE for Covid-19 immunization and took it from the facility. The patient past medical history and concomitant medication was not reported. On 01Jul2021, the patient experienced Diarrhea and vomiting, a week ago when took Pfizer vaccine. The patient stated that the schedule date for second dose was "22 or 21 days after". When probed if the patient was still experiencing adverse event to which he responded that he was still experiencing, everyday like, two times a day, diarrhea. The patient did not take any treatment for the reported events. The patient stated "Did you poop? This makes me happy. I watched videos women pooping." The patient hung up the call hence limited information was available over the call. The event outcome Diarrhea was not resolved while the outcome of the other event was unknown. No follow up attempts are needed; information about lot/batch number cannot be obtained.

Other Meds:

Current Illness:

ID: 1486329
Sex: M
Age:
State:

Vax Date: 01/28/2021
Onset Date: 01/01/2021
Rec V Date: 07/20/2021
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Symptoms: soreness in his left arm at the injection site; This is a spontaneous report from a contactable consumer (patient). A 73-year-old male patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Formulation: Solution for injection Batch/Lot number was not reported, Expiration Date was not reported), via an unspecified route of administration, administered in left arm on 28Jan2021 as dose 1, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient states that he received the first dose of the Pfizer Covid-19 vaccine on 28Jan2021 and had complaints of soreness in his left arm at the injection site on unspecified date in Jan2021 and the next day the soreness was pretty much gone. Patient received the second dose of the vaccine on 18Feb2021 and reported that he had no reactions. He was happy with the results of getting the Pfizer Covid-19 vaccine and "the first two seem to be working well". Patient was asking if it would be okay for him to get another dose of the Pfizer Covid-19 vaccine. Patient was asking if anyone has received the third dose of the Pfizer Covid-19 vaccine, are there any results for the third dose, and, if someone has received the third dose, has there been any side effects. The outcome of the event was recovering. Information on Lot/Batch information has been requested.

Other Meds:

Current Illness:

ID: 1486330
Sex: F
Age:
State: OR

Vax Date: 07/01/2021
Onset Date: 07/01/2021
Rec V Date: 07/20/2021
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Symptoms: Vertigo/room spinning; Blurry vision; General "fuzzy" head feeling; Headache going from back of head (left side) to the front.; Had a small rash that has since turned into the bruise; Had a small rash that has since turned into the bruise; Bruised knot at injection site still hasn't cleared; This is a spontaneous report from a contactable other healthcare professional (patient). A 28-years-old non-pregnant female patient received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot Number: EW0196) via an unspecified route of administration, in the left arm on 01Jul2021 (at the age of 28-years-old) as dose 1, single for COVID-19 immunization at pharmacy or drug store. The patient medical history included covid-19 from an unknown date and unknown if ongoing. Concomitant medication within 2 weeks of vaccination included ESTRADIOL, 0.5mg once daily taken for an unspecified indication, start and stop date were not reported. Allergies to medications, food, or other products included dilaudid and lortab. Prior to vaccination patient was diagnosed with COVID-19 and did not received any other vaccines within 4 weeks. Since the vaccination, the patient had not been tested for COVID-19. On 01Jul2021, the patient experienced headache going from back of head (left side) to the front started within an hour of receiving the vaccine and hadn't stopped since, and Still ongoing; and also had Bruised knot at injection site still hadn't cleared and had a small rash that has since turned into the bruise. On 03Jul2021, on day 3 after vaccine patient had Vertigo including blurry vision, room spinning, and general fuzzy head feeling started and lasted until day 7. The reporter assessed the events as non-serious The patient did not receive any treatment for the event. Outcome of the events vertigo, blurry vision and general fuzzy head feeling was recovered on 07Jul2021 and outcome of other events was not recovered.

Other Meds: ESTRADIOL

Current Illness:

ID: 1486331
Sex: F
Age:
State: AZ

Vax Date: 02/09/2021
Onset Date: 02/09/2021
Rec V Date: 07/20/2021
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Symptoms: continuing tinnitus in left ear; Swelling of the face; swelling of the lymph nodes in the jaw; This is a spontaneous report from a contactable consumer or other non hcp (patient). A 75-years-old female patient received BNT162B2 (Pfizer-Biontech Covid-19 Vaccine, Formulation: solution for injection, Batch/Lot Number EL3247, expiration date unspecified), via an unspecified route of administration, administered in Arm Left on 09Feb2021 11:30 as DOSE NUMBER UNKNOWN, SINGLE for COVID-19 immunization. The patient did not receive any other vaccines within 4 weeks prior to the COVID-19 vaccine. The patient was not diagnosed with COVID-19 prior to the vaccination. Medical history included penicillin and sulfa drug allergy from an unknown date. Concomitant medications included losartan (LOSARTAN) taken for an unspecified indication, from an unknown start date, levothyroxine sodium (LEVOTHYROXIN) taken for an unspecified indication, from an unknown start date. On 09Feb2021 12:15, the patient experienced continuing tinnitus in left ear with swelling of the face, swelling of the lymph nodes in the jaw. The patient was not treated for the events. Since the vaccination, the patient had not been tested for COVID-19. On an unspecified date in 2021, the events were resolved with sequelae.

Other Meds: LOSARTAN; LEVOTHYROXIN

Current Illness:

ID: 1486332
Sex: F
Age: 56
State: NV

Vax Date: 04/27/2021
Onset Date: 05/01/2021
Rec V Date: 07/20/2021
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Allergies: None

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Symptoms: Initially typical sore arm, low fever, then worsened to higher fever, cough, pounding heart, trouble breathing, stiff neck and shoulder, chills

Other Meds: None

Current Illness: None

ID: 1486333
Sex: F
Age: 41
State: FL

Vax Date: 01/22/2021
Onset Date: 02/01/2021
Rec V Date: 07/20/2021
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Symptoms: About a week after receiving the vaccine, I noted that I seemed to have some loss hearing. It has not improved as of yet.

Other Meds: Celexa 20 mg

Current Illness: None

ID: 1486334
Sex: F
Age:
State: MO

Vax Date: 06/30/2021
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Rec V Date: 07/20/2021
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Symptoms: Confusion; Trouble with walking straight; Vertigo; Feeling tired; Chills and fever; Cas in like brain fog, where I can't think clearly and I was having a bit of confusion; I still had dizziness for a week.; Chills; I can't think clearly; This is a spontaneous report received from a contactable consumer or other non-health care professional (Patient). A 24-years-old female patient received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Batch/Lot Number: EW0173), 1 via an unspecified route of administration, administered in Arm Left on 30Jun2021 (at the age of 24-years-old) as dose 1, single for covid-19 immunisation. Medical history included asthma. The patient's concomitant medications included, fluticasone propionate (FLOVENT), via an unspecified route of administration from an unspecified date (Batch/Lot number was not reported) to an unspecified date, at for an unspecified indication and it was like a steroid inhaler like I Quit taking after I got vaccine because I had feeling maybe that was why I was getting those such effects. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On unknown date, she experienced confusion and trouble with walking straight and vertigo that lasted for 1 week. It was the first dose and I had got the shot I started feeling tired which was expected, I started having fever, chills and then I started feeling like a brain fog and I got a little bit of confusion and I began to dizzy and so, like I supposed it does not need to be in order but so I started out and felt tired which was expected and I started to get chills and fever, again kind of expected that, then I started to get, I was in like brain fog, where I can't think clearly and I had a bit of few visions and then I was having a lot of trouble in walking straight for 3 hour. That continued for few hours and then I still had dizziness for a week and now I feel fine, that was my experienced. The reason for transfer would be that the caller had very severe case of side effects after her first dose of COVID Vaccine 10 days ago and she was also trying to get the information as much as possible regarding what side effects are to be expecting from her second dose which was going to be soon. Consumer stated, I just want to make sure I did not had a reaction that I was not supposed to had and now like it was okay. I know you can not give medical advice probably but I just want to make sure it was safe for me to get second dose. Consumer was informed about the role of Pfizer drug Safety and also informed that Pfizer Medical Information was the right department answer the question consumer have regarding the vaccine and offered the number. Consumer stated, I experienced with first shot of Pfizer (Covid-19 Vaccine) and if it was different from anybody else got, I want to know that I am safe to get the second shot and I do not if someone had side effect like that or something. Patient received vaccination facility in: Consumer stated, It was like, made like a building inside of our shopping centre specifically for getting vaccinated but it was through the hospital. So, it was a walk-in clinic type of thing. Patient received treatment as Tylenol for fever, but other than that I think I just took some vitamins like zinc, vitamin C and vitamin D3. I did not get like any other treatment. The outcome of the events dizziness, vertigo, difficulty in walking, confusion was reported as recovered on unknown date and while for other event was unknown. No follow-up attempts are possible. No further information is expected.

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ID: 1486335
Sex: M
Age:
State: NY

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Rec V Date: 07/20/2021
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Symptoms: Caller stated she heard of two people under 30 that got this side effect from the Pfizer covid 19 vaccine/ Caller stated she heard one of the side effects is a heart defect.; Kid across the street got the Pfizer vaccine and he is about 18 years old and had that heart inflammation; This is a spontaneous report from a contactable nurse from a Pfizer sponsored program COVAX US support. A 18-year-old male patient received unknown dose of bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, Solution for injection, Lot number and Expiration date: Not reported), via an unspecified route of administration on an unspecified date as dose number unknown, single (at the age of 18-years-old) for COVID-19 immunization. The patient medical history and concomitant medications were not reported. It was reported that reporter heard of two people under 30 that got side effect from the Pfizer covid 19 vaccine and heard one of the side effects is a heart defect. On an unknown date, the patient (Kid/Neighbor across the street) got the Pfizer vaccine and had heart inflammation and heart defect. Reporter wanted to know how many days after, would be seeing these side effects of heart inflammation. The outcome of events was unknown. Information on batch/lot number has been requested.

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Current Illness:

ID: 1486336
Sex: F
Age:
State: GA

Vax Date:
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Rec V Date: 07/20/2021
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Symptoms: loss of appetite; loss of taste; headaches; fatigue; This is a spontaneous report received from a contactable consumer or other non hcp (patients son). This consumer reported for mother. A 78-year-old female patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Batch/lot number was not reported) (age at vaccination was reported as 77 years) via an unspecified route of administration on an unspecified date in 2021 (Batch/Lot number not reported) as single dose for covid-19 immunization. Patient's Medical History including any illness at time of vaccination was reported as none. The patient's concomitant medications were not reported. The patient experienced loss of appetite, loss of taste, headaches, fatigue on an unspecified date. Additional context reported as report that his 78-year-old mother experienced side effects after administration of the fist dose of Pfizer Covid-19 Vaccine. The patient has already gone to the physician for the management of the symptoms. The patient was dosed with first dose of Pfizer Covid-19 Vaccine less than 2 weeks ago but does not have the actual date of administration or the Pfizer Covid-19 Vaccine Lot and things like that. The patient underwent lab tests and procedures which included chest x-ray: not have pneumonia on 09Jul2021. She does not have pneumonia. The clinical outcome of the events was not recovered. Information on the lot/batch number has been requested

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Current Illness:

ID: 1486337
Sex: M
Age:
State: NV

Vax Date: 06/25/2021
Onset Date:
Rec V Date: 07/20/2021
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Symptoms: a little discomfort; a little pain with heaviness feeling; This is a spontaneous report from a non-contactable consumer or other non-healthcare professional (parent). A 34-years-old male patient received bnt162b2 (BNT162B2, PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection), dose 1 via an unspecified route of administration on 25Jun2021 (Batch/Lot number and Expiry date was not reported) as DOSE 1, SINGLE for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date, the patient experienced a little discomfort and a little pain with heaviness feeling. Reporter reported that his son received vaccine and experienced a little discomfort for about 24 hours. He explained it as a little pain with heaviness feeling. It has eased up. Just a little discomfort now. Side effects that have been reported with the Pfizer-BioNTech COVID-19 Vaccine included muscle, injection site & arm pain. The reporter asked if you should return in 21 days for the second Pfizer Covid 19 Vaccine. In response it was stated that the Pfizer-BioNTech COVID-19 Vaccine is a suspension for intramuscular injection administered as a series of two doses (0.3 mL each) 3 weeks apart. Administer the Pfizer-BioNTech COVID-19 Vaccine intramuscularly. Reporter stated that she heard how the Johnson Vaccine may cause clotting. She thought she heard something about a female getting a clot to the brain and asked if Pfizer has any information for females with bleeding disorders or clots receiving the Pfizer Covid 19 Vaccine. The reporter also asked about the need for a booster dose (3rd dose) and if Pfizer is investigating the need for a booster dose. Response was provided as part of Pfizer and BioNTech continued efforts to stay ahead of the virus causing COVID-19 and circulating mutations, the companies provided an update on booster dosing on 9Jul2021. Please note that the use of a 3rd or booster dose is not recommended or authorized, and Pfizer does not suggest the use of the vaccine in any manner other than as described authorized. Initial data from the ongoing study of booster doses demonstrated a consistent tolerability profile and high neutralization titres against the wild-type virus (the naturally occurring non-mutated virus) and the Beta variant. It is thought that the effects seen against the Beta variant may also be seen in the Delta variant. We are doing studies to confirm this. We expect to publish the data soon in a peer-reviewed journal and submit to regulatory authorities in the coming weeks. Note to frontline: This FAQ should only be used specifically asks about the Pfizer statement on booster doses. For with general inquiries about booster doses, please refer to the titled Administration of More Than a 2-Dose Series (Booster Dose). should be referred to their for further discussion. The reporter stated that a family member who went in to get the vaccine a few days ago. They were given a receipt that has the vaccine should be given in the left arm and asked if the Pfizer Covid 19 Vaccine should only be administered in the left arm. In response it was stated that administer the Pfizer-BioNTech COVID-19 Vaccine intramuscularly. Also asked that according to the person who administered the Pfizer Covid 19 Vaccine said that it has to be mixed prior to giving, if the information is correct that the vaccine must be mixed prior to administering. In response it was stated that Add 1.8 mL of 0.9% Sodium Chloride Injection and administer the Pfizer-BioNTech COVID-19 Vaccine intramuscularly. The clinical outcome of the events was unknown. No follow-up attempts are possible. No information can be expected.

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Current Illness:

ID: 1486338
Sex: F
Age:
State: MO

Vax Date: 01/23/2021
Onset Date: 07/03/2021
Rec V Date: 07/20/2021
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Symptoms: On 03Jul2021, I contracted Covid, delta, variant; On 03Jul2021, I contracted Covid, delta, variant; This is a spontaneous report from a contactable nurse (Patient). A 53-year-old non-pregnant female patient received BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; formulation: Solution for injection, Lot Number: EL9262 and Expiry date was not reported) dose 2 via an unspecified route of administration in arm Left on 23Jan2021 09:00 (age at vaccination was 53-year-old) and dose 1 (Lot number: EL3246 and Expiry date was not reported) via an unspecified route of administration in right arm on31Dec2020 13:15 as single dose for covid-19 immunisation. The patient had no known allergies. Medical history included Hypothyroid, PFO, HCP from an unknown date and unknown if ongoing. Prior to the vaccination, the patient was not diagnosed with COVID-19. Post vaccination, the patient had tested for COVID-19. Concomitant medications in two weeks were included levothyroxine sodium (SYNTHROID), asa (ASA), riboflavin (RIBOFLAVIN), ergocalciferol, retinol (VITAMIN A + D), zinc (ZINC), magnesium (MAGNESIUM), topiramate (TOPAMAX) taken for an unspecified indication, start and stop date were not reported. The patient did not receive any other vaccines within four weeks. The patient was hospice that continues to take masking precautions, hand hygiene. On 03Jul2021 16:00 she contracted covid, variant. Due to events patient visited Emergency room/department or urgent care. Treatment received for the events was Promethazine, Albuterol inhaler, Tessalon pearls. The patient underwent lab tests and procedures which included PCR nasal Swab positive on 03Jul2021. The outcome of the event was recovering.; Sender's Comments: Based on the information in the case report, a possible causal relationship between events Covid-19 and suspect drug BNT162B2 cannot be excluded

Other Meds: SYNTHROID; ASA; RIBOFLAVIN; VITAMIN A + D; ZINC; MAGNESIUM; TOPAMAX

Current Illness:

ID: 1486339
Sex: F
Age:
State: NJ

Vax Date:
Onset Date: 04/13/2021
Rec V Date: 07/20/2021
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Symptoms: Muscle twitches in lower legs; This is a spontaneous report from a contactable consumer (Patient). A 58-years-old non-pregnant female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection; Batch/Lot Number: FR28744), via an unspecified route of administration, administered in Arm Left on an unspecified date as dose 1, single for COVID-19 immunization at other. The patient medical history included COVID-19. Concomitant medication(s) included losartan (LOSARTAN). The patient previously took Aleve. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. On 13Apr2021, patient experienced muscle twitches in lower legs. It was reported that no therapeutic measures were taken for the events experienced. The clinical outcome of event was not recovered. Follow-up attempts are needed. Information on the lot/batch available.

Other Meds: LOSARTAN

Current Illness:

ID: 1486340
Sex: U
Age:
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Rec V Date: 07/20/2021
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Symptoms: Arm pain; Runny nose; Watery eyes; Sneezing; Allergy; This is a spontaneous report from a contactable consumer (reported for self). A patient of unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as dose number unknown, single for covid-19 immunisation. The patient medical history and concomitant medications were not reported. On an unspecified date, the consumer stated that he went to get Pfizer Covid Vaccine on Tuesday evening around 6 o'clock and he just had like normal arm pain but probably on Thursday he started having like runny nose kind of like allergy running nose, watery eyes and he have been having and it's not improving it is getting worse. He has been getting runny nose, watery eyes and also sneezing. The outcome of the events was unknown. Information on the lot/batch number has been requested.

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Current Illness:

ID: 1486341
Sex: F
Age:
State: NC

Vax Date: 07/08/2021
Onset Date: 07/09/2021
Rec V Date: 07/20/2021
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Symptoms: Osteopenia; Have lost lot of height because of the osteoporosis; Had Ibuprofen but I don't take Ibuprofen because it is harder on stomach; Have lost lot of height because of the osteoporosis; Terrible headache; This is a spontaneous report from a contactable consumer (patient). A 71-year-old female patient received bnt162b2 (BNT162B2, solution for injection, Batch/Lot number EW176), via an unspecified route of administration on 08Jul2021, 3:00 (age at the vaccination 71-year-old) as DOSE 2, SINGLE for covid-19 immunisation. Medical history included haemorrhoids from an unknown date and unknown if ongoing. Concomitant medication(s) included hydrocortisone acetate (HYDROCORTISONE ACETATE) 25mg, taken for haemorrhoids, start and stop date were not reported. The patient experienced osteopenia on an unspecified date, have lost lot of height because of the osteoporosis on an unspecified date, terrible headache on 09Jul2021. The patient underwent lab tests and procedures which included bone density abnormal: osteoporosis on Jun2021. Therapeutic measures were taken as a result of osteopenia, have lost lot of height because of the osteoporosis. Treatment for Osteoporosis and Osteopenia consumer stated, its Vitamin D and calcium; had Ibuprofen but don't take Ibuprofen because it is harder on stomach. The outcome of events was persisting (not recovered) for Osteoporosis and Osteopenia; lost lot of height and terrible headache was unknown. Information on the lot/batch number has been requested

Other Meds: HYDROCORTISONE ACETATE

Current Illness:

ID: 1486342
Sex: M
Age:
State: NC

Vax Date:
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Rec V Date: 07/20/2021
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Symptoms: Shingles; This is a spontaneous report from a contactable consumer. A male patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, formulation: Solution for injection, Lot number and expiry date was not provided), via an unspecified route of administration, on an unspecified date as dose 2, single and bnt162b2 (formulation: Solution for injection, Lot number and expiry date was not provided), via an unspecified route of administration, on an unspecified date as dose 1, single, for covid-19 immunization (had both doses of the vaccine). The reason for no lot number was stated as the complainant did not have the product with them at the time of call. The patient medical history and concomitant medications were not reported. It was stated that, the reporter met a younger man that also developed shingles on an unspecified date, after the Pfizer covid vaccine. The reporter said that her husband had a lot more shingles compared to the young man (husband case of shingles was a lot worse). Reportedly, the man had pictures of his shingles. The outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1486343
Sex: F
Age:
State: MD

Vax Date:
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Rec V Date: 07/20/2021
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Symptoms: hives on her arms, torso, and thighs; This is a spontaneous report from a contactable consumer or other non hcp. This consumer reported for a female patient. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and Expiry date not reported), via an unspecified route of administration on an unspecified date as dose number unknown, single for COVID-19 immunization.The patient's medical history and concomitant medications were not reported. Report was not related to a study or programme. On an unknown date, after taking the vaccine, the patient experienced hives. It was reported that she googled Covid vaccine and hives. was the first thing that popped up with 9 people. There was this woman that said she took Pfizer COVID and had hives. On the second day she got hives on her arms, torso, and thighs. They told the woman to take an antihistamine and then moved on to next call. Caller stated she didn't have information for that woman and did not wish to do a report for her. The outcome of event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1486344
Sex: U
Age:
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Rec V Date: 07/20/2021
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Symptoms: face swelled; Rash; This is a spontaneous report received from contactable consumer (the patient). A patient of unspecified age and gender received the received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, Batch/Lot number and expiration date were not reported), via unspecified route of administration, on an unspecified date, as single dose, for COVID-19 immunization. The patient's medical history and concomitant medication were not reported. On an unspecified date, patient experienced face swelled and rash. Patient stated that, i was calling to reaction because I had been having reaction to Pfizer and I just want to know how proceed with my second shot, my second shot is 19 of this month 19Jul2021 (Further clarification unknown) and doctor had helped me with that so much so my face swelled and had a bad rash, my doctor put in for it. Outcome of the events was unknown. Information about lot/batch number has been requested.

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Current Illness:

ID: 1486345
Sex: U
Age:
State:

Vax Date: 07/07/2021
Onset Date: 07/01/2021
Rec V Date: 07/20/2021
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Symptoms: I have body ache and headache; It's almost like a tension headache on top of my head.; I have body ache and headache; This is a spontaneous report from contactable consumer (patient). A patient of an unspecified age and gender received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot Number was not reported), via an unspecified route of administration on 07Jul2021 at 05:00 PM (48 hours ago on Wednesday at 5pm) as dose number unknown, single for COVID-19 immunization. Medical history and concomitant medications were not reported. On an unspecified date in Jul2021, the patient experienced body ache and headache the 1st 24 hours. Patient had a very bad headache. It was almost like a tension headache on top of the head. Patient wanted to know if that was normal. The outcome of the events was unknown. Follow-up attempts are needed; information about lot/batch number can be obtained.

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Current Illness:

ID: 1486346
Sex: M
Age:
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Rec V Date: 07/20/2021
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Symptoms: Throat Hurts and he has a lot of yellow mucus; Throat Hurts and he has a lot of yellow mucus; This is a spontaneous report from a contactable consumer. This contactable consumer (Patient's Parent) reported for a 24 years old male patient that he received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot Number, Expiry Date, NDC Number, UPC Number: Unknown), via an unspecified route of administration on an unspecified date as DOSE NUMBER UNKNOWN, SINGLE (at the age of 24 years old) for covid-19 immunization. The patient medical history and concomitant medications were not reported. He had Pfizer COVID shot a little over 2 weeks ago and he said his throat really hurts and he had a lot of yellow mucus. He wondered whether it was a known side effect or it could be just a cold and he wanted to know whether anyone reported such side effect. The outcome of all events were unknown. Information on Lot/Batch number has been requested.

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Current Illness:

ID: 1486347
Sex: M
Age:
State: MN

Vax Date: 03/01/2021
Onset Date:
Rec V Date: 07/20/2021
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Symptoms: Had fever of 102.6 for 3 days and then the fever drop down to 100; He'd work a little bit and then had to lay down and take a nap; This is a spontaneous report from a contactable consumer, the patient. This consumer reported for a male patient (husband). A 78-year-old male patient received second dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Formulation: Solution for injection, Lot/Batch number: Unknown), via an unspecified route of administration in right arm on an unknown date in Mar2021 as DOSE 2, SINGLE for COVID-19 immunization. Medical history was not reported. The patient's concomitant medications included aspirin and Tamasol which was a blood thinner. Patient previously received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) on 23Feb2021 for COVID-19 immunization. The second shot was 2 weeks later, now she could not remember the date on that. It was the beginning of Mar (about 3 weeks ago) and he had no reaction to the injection or the injection site. Patient had fever of 102.6 for 3 days and then the fever dropped down to 100 and then slowly after the second for two weeks, patient had fever and fatigue. Patient would work a little bit and then had to lay down and took a nap, he had been to the doctor 4 different times and they ran all kinds of test and they never came up with anything. Chest X-rays were done to make sure there was nothing going on with his chest. They checked him mosquito bites and all kinds of different diseases and stuff and nothing, absolutely nothing showed up. The patient did not receive any treatment. The outcome of the events was unknown. Information on the lot/batch number has been requested.

Other Meds: ASPIRIN [ACETYLSALICYLIC ACID]

Current Illness:

ID: 1486348
Sex: F
Age:
State:

Vax Date:
Onset Date:
Rec V Date: 07/20/2021
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Symptoms: Aching/Sore; Very sick; This is a spontaneous report from a contactable consumer. This consumer (Patient Husband) reported for a female patient. A female patient of an unspecified age received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE, formulation: solution for injection, Batch/Lot number was not reported), via an unspecified route of administration on an unspecified date as DOSE 1, SINGLE for covid-19 immunisation. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced aching/sore, very sick. Reporter is very sick right now by the aching and sore. So, we are trying to see how long is it supposed to last, whether she needs to go to the emergency room now what she needs to do. Reporter stated, I am calling because me and my wife couldn't get our second round of the vaccine (unspecified vaccine) yesterday (split not made). Reporter was informed that Pfizer Medical Information is the right department to answer this question and informed about the role of Pfizer Drug Safety. Further probing could not be done as the reporter hung up the call abruptly. Hence limited information available over the call. The outcome of the events was unknown. QR Comment: Split to be made which was not made by the Call handler.

Other Meds:

Current Illness:

ID: 1486349
Sex: F
Age:
State: FL

Vax Date:
Onset Date: 02/01/2021
Rec V Date: 07/20/2021
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Symptoms: extremely tired; This is a spontaneous report from a contactable physician (reporter's wife). A female patient of an un-specified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number/ expiry date not reported), via an unspecified route of administration on unspecified date in 2021 at dose 2, single for covid-19 immunization. The patient medical history and concomitant medication were not reported. The patient previously took first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, lot number/ expiry date: not reported), via an unspecified route of administration on unspecified date for covid-19 immunization. On an unspecified date in Feb2021 patient felt extremely tired the whole day. Reporter stated that he did have was one week after the second shot he and his wife both felt extremely tired the whole day. Patient vaccination was a week ahead of his. She only had the tiredness for 24 hours. The report was not related to any study or pro-gram. The outcome of event was recovered on an unspecified date in Feb2021. Information on Lot/Batch number has been requested

Other Meds:

Current Illness:

ID: 1486350
Sex: M
Age:
State: KY

Vax Date: 07/10/2021
Onset Date: 07/10/2021
Rec V Date: 07/20/2021
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Symptoms: Having just little mild ache at, where the shot was given; It is just mild pain; This is a spontaneous report from a contactable consumer (patient, self-reported). A 73-years-old male patient received first dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number: EW0198 and expiry date was not reported), via an unspecified route of administration, on 10Jul2021, as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient stated that just had his first Pfizer shot this afternoon and he did not see anything in papers he got with that whether alcohol affects it. The patient reported that on 10Jul2021, he having just little mild ache at, where the shot was given; It was just mild pain. When clarified the concern consumer stated he had his first Pfizer shot this afternoon he did not see anything about if there was any interaction of alcohol with it. Outcome of the event was unknown. Follow-up attempts are needed. Further information is expected.

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Current Illness:

ID: 1486351
Sex: M
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Onset Date:
Rec V Date: 07/20/2021
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Symptoms: He is running a low grade temperature; This is a spontaneous report from a contactable consumer (reporter's husband). A male patient of an unspecified age received a dose of BNT162B2 (PFIZER-BIONTEC COVID-19 mRNA VACCINE, Solution for injection, lot number and expiry date were not reported), via an unspecified route of administration, on an unspecified date, as a single dose for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. The patient reported that on an unspecified date, he was running a low grade temperature. The patient's wife (reporter) asked should she be alarmed about it or should she be worried, and Should she take him to the emergency room because he was running a low-grade temperature. Outcome of the event was unknown. Information on the lot/batch number has been requested.

Other Meds:

Current Illness:

ID: 1486352
Sex: M
Age:
State:

Vax Date: 07/09/2021
Onset Date:
Rec V Date: 07/20/2021
Hospital:

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Symptoms: Chest pain; This is a spontaneous report from a contactable consumer reported for a patient. A 15-years-old male patient received an unknown dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Lot number: unknown, Expiration date: unknown) via an unspecified route of administration, administered at an unspecified anatomical location on 09Jul2021 (age at vaccination was unknown) as dose number unknown, single for COVID-19 immunization. The patient's medical history and concomitant medications were not reported. On an unspecified date, the patient experienced chest pain. The reporter stated, the patient got the vaccine 24 hours ago and he just mentioned he has little side effect, pain the chest pain and asked what he could do. The reporter was informed about Pfizer drug safety. The reporter was informed about the Pfizer Medical Information Department. The outcome of the event was unknown.

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Current Illness:

Total 2021 VAERS Injuries: 599,999

Page last modified: 03 October 2021 5:28pm