VAERS Reports gen6204

VAERS 1650875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 6204

moderat

Staat: TX
Alter: -
Geschlecht: M
Eingang: 28.08.2021
Impfdatum: 18.03.2021
Beginn: 30.03.2021
Tage bis Beginn: 12,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain

Symptomtext

Chest pain; This is a spontaneous report from a contactable consumer or other non hcp. A 78-years-old male patient received second dose bnt162b2 (BNT162B2, Solution for injection, Batch/Lot Number: 6204) via an unspecified route of administration in Arm Left on 18Mar2021 10:45 as DOSE 2, SINGLE for covid-19 immunisation (at pharmacy). Patient didn't had covid prior to vaccination, patient didn't receive other vaccines within 4weeks prior to vaccination, patient received other medications lisinopril, allopurinol, foltanx, cartia xt, Motrin within 2weeks. Medical history included arthritis from an unknown date and unknown if ongoing, herpes zoster from 04Feb2020 to an unknown date, analgesic therapy from an unknown date and unknown if ongoing. Concomitant medications included lisinopril (LISINOPRIL) taken for an unspecified indication, start and stop date were not reported; allopurinol (ALLOPURINOL) taken for an unspecified indication, start and stop date were not reported; calcium levomefolate, mecobalamin, pyridoxal phosphate (FOLTANX RF) taken for an unspecified indication, start and stop date were not reported; diltiazem hydrochloride (CARTIA XT) taken for an unspecified indication, start and stop date were not reported; ibuprofen (MOTRIN [IBUPROFEN]) taken for analgesic therapy, start and stop date were not reported; paracetamol (TYLENOL) taken for analgesic therapy, start and stop date were not reported. Patient had no allergies. Patient previously received first dose bnt162b2 (BNT162B2, Solution for injection,Batch/Lot Number:EN 6202) via unspecified route of administration on 25Feb2021 15:45 as DOSE 1, SINGLE for covid-19 immunisation. The patient experienced chest pain on 30Mar2021 14:00. Therapeutic measures were taken as a result of chest pain was antiviral and pain prescription. The outcome of the event chest pain was recovering. No follow-up attempts are possible; No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthritis; Pain relief; Shingles
Andere Medikamente: LISINOPRIL; ALLOPURINOL; FOLTANX RF; CARTIA XT; MOTRIN [IBUPROFEN]; TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 1228332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 6204

moderat

Staat: NY
Alter: 73,0
Geschlecht: M
Eingang: 19.04.2021
Impfdatum: 25.02.2021
Beginn: 04.03.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Gait disturbance Mobility decreased

Symptomtext

Intense pain in right knee and right hip. Caused difficulty moving right leg or walking. Only slightly abated after 2 months

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension
Andere Medikamente: Atorvastatin Ezetimibe Losartan
Allergien: none
Vorherige Impfungen: -

VAERS 1142595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 6204

moderat

Staat: TX
Alter: 52,0
Geschlecht: M
Eingang: 28.03.2021
Impfdatum: 28.03.2021
Beginn: 28.03.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypertension Hypoaesthesia Injection site pain Injection site swelling Paraesthesia Pruritus

Symptomtext

High Blood Pressure: 135-91, numbness and tingling in my left hand, and itchiness in my right foot. I also experienced pain and swelling in the injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1117121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 6204

moderat

Staat: -
Alter: 32,0
Geschlecht: M
Eingang: 19.03.2021
Impfdatum: 17.03.2021
Beginn: 18.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dyspnoea

Symptomtext

Difficulty breathing for 24 hours, starting 12 hours after vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1684382

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 6204

mild

Staat: TX
Alter: 55,0
Geschlecht: M
Eingang: 09.09.2021
Impfdatum: 15.03.2021
Beginn: 01.05.2021
Tage bis Beginn: 47,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Limb injury Pruritus Vaccination site mass

Symptomtext

got a lump at the injection site, left arm; itching a lot; he doesn't know if it's related or not, but something stung him on his thumb.; This is a spontaneous report from a contactable consumer. A 55-years-old male patient received bnt162b2 (BNT162B2), dose 2 via an unspecified route of administration, administered in Arm Left on 15Mar2021 12:15 (Batch/Lot Number: 6204) as 2ND DOSE, SINGLE for covid-19 immunisation. Medical history included ongoing diabetes mellitus, bronchiectasis from an unknown date and unknown if ongoing. Concomitant medication included metformin (METFORMIN) taken for diabetes mellitus, start and stop date were not reported; risperidone (RISPERIDONE) taken for affective disorder, start and stop date were not reported; colecalciferol (VITAMIN D3) taken for asthenia, start and stop date were not reported; cyanocobalamin, folic acid (VITAMIN B12 & FOLIC ACID) taken for asthenia, start and stop date were not reported. The patient experienced itching a lot on 07May2021, got a lump at the injection site, left arm on 09May2021, he doesn't know if it's related or not, but something stung him on his thumb on May2021. The outcome of the event itching a lot and got a lump at the injection site, left arm was not recovered and outcome of the event something stung him on his thumb was unknown. Additional Context: Caller stated that he's got a lump at the injection site of the Pfizer vaccine. Caller verifies it was the Pfizer Covid Vaccine. Caller states it itches a lot too. Pfizer Covid Vaccine: First Dose he received the first one 22Feb2021. Caller provided LOT: EN6201. Caller unsure of Expiry date, NDC. Caller states received as injection in left arm. Caller received between 12 and 2pm, he doesn't really remember. Caller states he had the appointment at 10 and had to stand in line for hours to get it. Pfizer Covid Vaccine: Second Dose: Caller states he received the second dose 15Mar2021. Caller states on the card, they just wrote Pfizer scribble, the two letters are indecipherable. Caller states all it says is Pfizer 6204 and the rest is just scribbled. Caller verifies it is handwritten. Caller states no expiry date or NDC on card. Caller states received second dose at 1215pm in his left arm. Address: Caller states he must get permission from his phone to look it up. Caller states he moved so he doesn't know it yet. Caller states he doesn't live at a permanent address but can give his parents address if Pfizer needs that. Itching; lump: Caller states he started itching about 3 days ago and now it's a lump because he was scratching it. Prescribing Healthcare Professional: Caller states he doesn't have a primary care doctor, he is just starting a new job. Caller states he doesn't know if it's related or not, but something stung him on his thumb. Caller states it was like an ant bite, but serious. Caller states at first, he thought it was a brown recluse, it was the same arm, on his left thumb. Caller states it turns out it was just an ant. No follow up attempt is needed: No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Diabetes (Verbatim: diabetes)
Vorgeschichte: Medical History/Concurrent Conditions: Bronchiectasis
Andere Medikamente: METFORMIN; RISPERIDONE; VITAMIN D3; VITAMIN B12 & FOLIC ACID
Allergien: -
Vorherige Impfungen: -

VAERS 1118698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 6204

mild

Staat: TX
Alter: 37,0
Geschlecht: F
Eingang: 28.08.2021
Impfdatum: 10.03.2021
Beginn: 10.03.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Dizziness Full blood count Headache Impaired work ability Metabolic function test Illness Laboratory test Nausea Pain in extremity SARS-CoV-2 test negative SARS-CoV-2 test

Symptomtext

dizziness was so severe; So sick; Nausea; Sore Arm; This is a spontaneous report from a contactable nurse (patient). A 37-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE), dose 1 via an unspecified route of administration, administered in Arm Left on 10Mar2021 13:00 (Batch/Lot number was not reported) as DOSE 1, SINGLE for covid-19 immunisation. Medical history included asthma, Low Immune System, Pretty Bad Eczema, all ongoing. Concomitant medication included methylprednisolone acetate and other unspecified medicines. The patient had a historical vaccine of Tyhoid vaccine from 2006 to 2006 for Immunization and it hurt way worse. Patient just had a sore arm that day (10Mar2021). On 11Mar2021 04:00, 16 hours after taking it, she got up and was dizzy and nauseated. She went to the ER on day 6 and she saw 2 doctors that following week. They were figuring out what was going on, she was so sick and the dizziness was so severe. She was told at that time not to get the second vaccine by her doctor and the ER doctor said even with her side effects, she needs to get the vaccine. Her primary care physician after said he is not sure if she should get it or not because of the reaction she had to the first vaccine and she had never had Covid or antibodies. She had just fully recovered by the 3 weeks when she was supposed to get her second one, so she was planning to get the second dose at 6 weeks. She didn't because one doctor said no and one said yes. Her reaction is unlike any of her patients. She wants to be fully vaccinated, she is scared to death.She does have severe asthma, and she has been admitted to the ICU before with it. She is not around Covid, she works from home. Treatment: At the ER, they gave her fluids and drew lab work, but it was all okay. They gave her antibiotics to cover the bases. They also gave her Meclizine and it didn't help. They also gave her nausea medication in the ER that Tuesday 16Mar2021. She was treated in the ER and released. She also had Covid tests that were negative twice. She had a steroid injection 9 days before the Covid Vaccine. Caller states it is a Trigger Point Injection, she believes it was Methylprednisolone, a small dose into her muscle. For 16 days she was sick. She was able to work from home some, but she missed several days of work because it was too bad to work. She is trying to figure out now with new variant and her son going to withheld where no one will be wearing masks. No one has that severe of dizziness that she knows of. Blood Work, was all okay. The outcome of the events was recovered. The lot number for the vaccine, [BNT162B2], was not provided and will be requested during follow up.; Sender's Comments: There is a reasonable possibility that the events nausea and pain in extremity were related to BNT162b2 based on known drug safety profile. Based on the close temporal relationship, the association between the events dizziness and illness can not be fully excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Date: 20210316; Test Name: Lab Work; Result Unstructured Data: Test Result:Okay; Test Date: 20210316; Test Name: Covid test; Test Result: Negative ; Comments: had Covid tests that were negative twice.
Aktuelle Erkrankungen: Asthma (Verbatim: Asthma); Eczema (Verbatim: Pretty Bad Eczema); Immune system disorder (Verbatim: Low Immune System)
Vorgeschichte: -
Andere Medikamente: METHYLPREDNISOLONE [METHYLPREDNISOLONE ACETATE]
Allergien: -
Vorherige Impfungen: -

VAERS 1482042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 6204

mild

Staat: NY
Alter: 63,0
Geschlecht: F
Eingang: 18.07.2021
Impfdatum: 22.03.2021
Beginn: 25.03.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Inappropriate schedule of product administration Rash macular

Symptomtext

First dose on 04Mar2021 and Second dose on 22Mar2021; Red Blotchy Rash; This is a spontaneous report from a contactable consumer, the patient. A 63-year-old non pregnant female patient received second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: 6204), via an unspecified route of administration in the left arm on 22Mar2021 (at the age of 63-years-old), as a single dose for COVID-19 immunisation. Medical history included rheumatoid arthritis, osteoarthritis and asthma. The patient was allergic to penicillin, pecans, bananas and latex. Concomitant medications included methotrexate (MANUFACTURER UNKNOWN), adalimumab (HUMIRA), paracetamol (TYLENOL) and pseudoephedrine hydrochloride (SUDAFED); all from unknown dates for unspecified indications. The patient previously received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot number: 6202), via an unspecified route of administration in the right arm on 04Mar2021 (at the age of 63-years-old), as a single dose for COVID-19 immunisation. Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not tested for COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. On 25Mar2021, the patient experienced red blotchy rash. The patient received first dose on 04Mar2021 and second dose on 22Mar2021 (Inappropriate schedule of vaccine administered). The patient did not receive any treatment for blotchy rash. The clinical outcome of the event red blotchy rash was not recovered and of the inappropriate schedule of vaccine administered was unknown at the time of this report. No follow-up attempts are needed. No further information is expected

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash macular
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to nuts (known allergies: penicillin, pecans, bananas, latex); Asthma; Fruit allergy (known allergies: penicillin, pecans, bananas, latex); Latex allergy (known allergies: penicillin, pecans, bananas, latex); Osteoarthritis; Penicillin allergy (known allergies: penicillin, pecans, bananas, latex); Rheumatoid arthritis
Andere Medikamente: METHOTREXATE; HUMIRA; TYLENOL; Sudafed
Allergien: -
Vorherige Impfungen: -

VAERS 1118396

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 6204

mild

Staat: SC
Alter: 70,0
Geschlecht: F
Eingang: 20.03.2021
Impfdatum: 18.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Rash Rash erythematous Rash pruritic

Symptomtext

on Friday 03/18/21 I woke at 6:00 AM with itching and upon inspecting my body found I had a red itchy rash on the trunk of my body front and back. Very, very little rash on my upper arms and upper thighs that didn't seem to present until Sat. morning 3/19/21. I did have allergy testing within the month prior which reaffirmed my cat allergy but saw improvement from testing 5 years ago. I also received my regular allergy shots 2/23/21 and 3/15/21. I was given ordansetron for nausea at the ER after gall stone diagnosis on 3/13/21 of which I took two tablets spaced according during the day 3/17/21. I was feeling well on 3/18/21 when I received my shot and was excited to get my Covid 19 vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: gall stones diagnosis 3/13/2021
Vorgeschichte: asthma, treated blood pressure and cholesteral
Andere Medikamente: triamterene/HTCZ 37.5/25, lisinopril .5, fenofibrate 160 mg,
Allergien: cats, lipitor, sensitive to adhesives
Vorherige Impfungen: -

VAERS 1118040

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 6204

mild

Staat: AL
Alter: 53,0
Geschlecht: M
Eingang: 20.03.2021
Impfdatum: 18.03.2021
Beginn: 19.03.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Headache Inappropriate schedule of product administration Injection site pain Nausea Pain Pyrexia

Symptomtext

Received the vaccine on day 15 after the first vaccine. Experienced pain at injection site. Fever, nausea, severe fatigue, headache and severe body aches. Lasted approx 12 to 14 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: DMII
Andere Medikamente: Metformin Zyrtec
Allergien: None
Vorherige Impfungen: -