VAERS Reports EN6701

VAERS 2633536

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6701

moderat

Staat: MS
Alter: 73,0
Geschlecht: F
Eingang: 18.05.2023
Impfdatum: 01.11.2022
Beginn: 04.03.2023
Tage bis Beginn: 123,0
Dosis: 2
Route/Site: SYR / LA

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

Asthenia COVID-19 Cough Loss of personal independence in daily activities Malaise Mobility decreased Oropharyngeal pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

woke up on last day of a 7 night cruise with a sore throat. Drove home for 2 days with running nose and coughing. Treated with over the counter medicine and finally called the doctor on 6 after not getting any better. He told me to continue what I was doing as it was too late to treat for COVID. After another day or two went to a walk in clinic. Received a shot, and perscription for a steroid and cough medicine. Continued to take my medicine but was still sick with horrible cough and bad congestion. Was in bed about 2 1/2 weeks not able to do anything. After I was able to be up I continued to have no energy for about 2 months. I now feel back to normal and able to do the things I enjoy. I am NEVER sick and I think that is the reason it hit me so hard.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: at home covid test on March 6, 2023 - tested positive Went to walk in clinic and took another Covid test on March 10, 2023 - tested positive
Aktuelle Erkrankungen: none
Vorgeschichte: High blood pressure controlled with medicine High cholesterol controlled with medicine High pressure in eyes controlled with medicine
Andere Medikamente: Bupropion HCL XL 300 mg Lisinopril 40 mg tablet Estradiol 2 mg tablet Latanoprost 0.005% eye drops Atorvastatin 20 mg tablet Multi vitamin Calcium twice daily 800mg/800 vitamin D3 Glucosamine chondroitin 1500/1200 stool softener zinc 50 mg
Allergien: none
Vorherige Impfungen: -

VAERS 1750457

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge En6701

moderat

Staat: CA
Alter: 81,0
Geschlecht: F
Eingang: 30.09.2021
Impfdatum: 28.09.2021
Beginn: 29.09.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain Diarrhoea Fatigue Pain in extremity

Symptomtext

Severe chest pains that lasted about 5 minutes also diarrhea . Pain in right arm. Fatigue also.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: prolapse
Andere Medikamente: no
Allergien: sulfa drugs
Vorherige Impfungen: flu vaccine 10 years ago .severe nausea

VAERS 1259714

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6701

moderat

Staat: CA
Alter: 75,0
Geschlecht: M
Eingang: 26.04.2021
Impfdatum: 25.01.2021
Beginn: 13.03.2021
Tage bis Beginn: 47,0
Dosis: 2
Route/Site: SYR / RA

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

Hypoaesthesia Paraesthesia Skin discolouration

Symptomtext

3/13, 26 days after receiving second vaccine Two entire fingers went white, looked bloodless, slightly numb and tingly. After about 10 minutes it returned to normal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Calcium Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 1259664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6701

moderat

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 26.04.2021
Impfdatum: 25.01.2021
Beginn: 17.04.2021
Tage bis Beginn: 82,0
Dosis: 2
Route/Site: SYR / RA

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

Hypoaesthesia Paraesthesia Skin discolouration

Symptomtext

4/17, 61 days after receiving second vaccine Tip of right index finger went white, looked bloodless, slightly numb and tingly. After about 10 minutes it returned to normal

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None Date stated was for first dose. Second dose was 2/15/2021
Andere Medikamente: Calcium Vitamin D
Allergien: Sensitivity to latex
Vorherige Impfungen: -

VAERS 1147698

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6701

mild

Staat: WA
Alter: 70,0
Geschlecht: M
Eingang: 30.03.2021
Impfdatum: 10.02.2021
Beginn: 23.02.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: - / RA

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

Rash

Symptomtext

Systemic rash covering part of arms & torso; This is a spontaneous report from a contactable consumer (patient). A 70-years-old male patient received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: EN6701), via an unspecified route of administration, administered in the right arm on 10Feb2021 at 15:00 (at the age of 70-years-old) as a single dose for COVID-19 immunisation. Medical history included coronary heart disease (CHD), nocturia, hypertension, lumbago, cervicalgia and allergies to statins. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. Concomitant medication included evolocumab (REPATHA) 140mg twice a month and other unspecified medications. The patient experienced systemic rash covering part of arms & torso on 23Feb2021. No treatment was received for the systemic rash. The outcome of event systemic rash was recovering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cervicalgia; Coronary heart disease; Drug allergy; Hypertension; Lumbago; Nocturia
Andere Medikamente: REPATHA
Allergien: -
Vorherige Impfungen: -

VAERS 1015757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6701

mild

Staat: MO
Alter: 67,0
Geschlecht: F
Eingang: 09.02.2021
Impfdatum: 05.02.2021
Beginn: 08.02.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / LA

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

Headache Pain Pain of skin Rash

Symptomtext

Day 2 - Had a bad headache but that went away by day 3. Day 4 I started to notice a tenderness in my right thigh and a rash started to appear. The entire front of my thigh is very tender. Plus my body just seems to feel achy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Atorvastatin 20 mg,
Allergien: none that are known.
Vorherige Impfungen: -

VAERS 1512046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6701

gering

Staat: OH
Alter: 73,0
Geschlecht: F
Eingang: 29.07.2021
Impfdatum: 24.02.2021
Beginn: 27.05.2021
Tage bis Beginn: 92,0
Dosis: 2
Route/Site: OT / RA

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

Gout Peripheral swelling

Symptomtext

Gout; red, swollen, and very ugly, but it wasn't her big toe; This is a spontaneous report from a contactable consumer (patient). This is report 1 of 2. A female patient of 73-year-old age received second dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was EN 6701, Expiration date- Jun2021), second dose on right arm via an intramuscular route of administration on 24Feb2021, 11:15 as single dose for COVID-19 immunization. Medical history was none. She is allergic to aspirin, the antibiotic penicillin, and a medication she can't remember the name of , but it was a pill for an upset stomach that sent her to the hospital in anaphylactic shock- she confirms this anaphylactic reaction was more than 17 years ago. She confirms she has no name for this medication and has no NDC, Lot number or expiry date for any of these products, it's been more than 10 years for all 3 of these medications. She states she didn't use to be allergic to aspirin but it happened about 20 years ago. No concomitant medication reported. The caller explains she takes her regular prescribed medications, nothing new or added within the 2 weeks leading up to the gout. Previously she received first dose of bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/Lot number was EL 9265, Expiration date-May2022), via Intramuscular injection route of administration in left arm on 03Feb2021 for COVID-19 immunization. Patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine and no AE prior vaccination. She got her shots in February, both of them. Then, she got gout really bad at the end of May. She has never had gout before. She states she spoke to two people last week who said they had never had gout before the vaccine and had it after, and she was told to call to let Pfizer know. Caller confirms the gout happened on a Thursday. She clarifies the gout was starting up her leg. She later clarifies she didn't start feeling the gout until about 4pm in the afternoon on Thursday, 27May2021. It was red, swollen, and very ugly, but it wasn't her big toe. Everybody she knows had gout in their big toe. the caller states its still red but its much better. The foot doctor said it will take a while until the redness goes away. She mentions she will see the Rheumatologist again in August. The caller states the Tuesday, she was prescribed something, but doesn't know what it was. By Thursday, it was in her veins. She clarifies the gout was starting up her leg. She clarifies further her blood vessels were highlighted with red like she had an infection. She called got in and got into see the foot doctor that Friday morning and had to go to the surgical center to treat by draining it. She states she was told she had Tophi which is a part of the gout and an infection. A week and a half later she was at the Rheumatologist. Patient visited Physician Office for AE. She should have gone to emergency room but she didn't. Caller states she believes the Lot number is EN6701, she thinks the fourth digit is a 7, but it could be a 2, but she doubts it. She confirms she believes the Lot number reads EN6701. The outcome of event was recovering. Follow-up attempts are needed. Further information is requested.

Weitere VAERSDATA-Felder

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

VAERS 1405816

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge EN6701

gering

Staat: CA
Alter: 85,0
Geschlecht: F
Eingang: 17.06.2021
Impfdatum: 20.02.2021
Beginn: 15.03.2021
Tage bis Beginn: 23,0
Dosis: 1
Route/Site: - / LA

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

Asthenia Disease recurrence Escherichia sepsis

Symptomtext

The patient experienced occurrence of E.coli sepsis on 15Mar2021 and ended up in hospital; The patient experienced occurrence of E.coli sepsis on 15Mar2021 and ended up in hospital; The patient got so weak; This is a spontaneous report received from a contactable retired registered nurse (patient). An 85-year-old female patient received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration, administered in arm left (left shoulder, but not certain) on 20Feb2021 11:30 (Batch/Lot Number: EN6701) at age of 85-year-old at single dose for COVID-19 immunization (the patient didn't want to catch COVID and wanted to have antibodies to fight it). Vaccine was not administered at known Facility. Medical history included first hospitalization for E.coli (Escherichia coli) sepsis was in Feb2021, prior to receiving the first dose Pfizer COVID Vaccine, the patient received more antibiotics from home health and the patient was in the hospital for five days from 01Feb2021 to 05Feb2021 and had the last antibiotic on 09Feb2021. Concomitant medications included ceftriaxone (ROCEPHIN) and cefalexin (KEFLEX) taken for E.coli sepsis from 15Mar2021 to 02Apr2021. Prior Vaccinations (within 4 weeks) there was not any other vaccinations within four weeks prior to the first administration date of the suspect vaccine. The patient experienced occurrence of E.coli sepsis on 15Mar2021 and ended up in hospital. The patient had been in the hospital again after receiving the first dose Pfizer COVID Vaccine for the patient's second occurrence of E. Coli sepsis. The patient was in rehab by 01Apr2021 and was taken by medical transport at the hospital to receive her second dose Pfizer COVID Vaccine. The patient clarified she had E.coli sepsis twice. The patient's first hospitalization for E.coli sepsis was from 01Feb2021 to 05Feb2021, prior to receiving the first dose Pfizer COVID Vaccine. The caller's second hospitalization was from 15Mar2021 to 02Apr2021, the patient was in rehab for three weeks. The patient stated she was no longer on any antibiotics. The patient was on ceftriaxone first and then cefalexin, IV. The caller was in the emergency room on 15Mar2021 and they admitted the patient at health facility for three days, then they transported the patient to a bed in the rehab area because the patient needed another 21 doses of antibiotics and the patient needed to learn to walk again. The patient got so weak. The patient was discharged on 02Apr2021. The event E.coli sepsis required visit to emergency room and physician office. Relevant tests were none. The outcome of the events was unknown.; Sender's Comments: Based on the limited information in the case, a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported E.Coli Sepsis. 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: Asthenia
Hospital-Tage: 18,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Escherichia sepsis (first E.coli Sepsis occurrence, prior to receiving the first dose Pfizer Covid Vaccine)
Andere Medikamente: ROCEPHIN [CEFTRIAXONE]; KEFLEX [CEFALEXIN]
Allergien: -
Vorherige Impfungen: -