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Reporte zur Charge FJ5683

Verknuepft ueber VAERS_ID mit VAERSDATA, Vax und Symptoms

385Reporte angezeigt
3Todesfaelle
29Hospitalisiert
5Lebensbedrohlich
9Bleibende Schaeden
TX 57 CA 57 NY 48 PA 23 NJ 16 VA 15 PR 13 WA 11 OR 10 MN 9 MI 9 FL 8

VAERS 2604554

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

kritisch
Staat
-
Alter
73,0
Geschlecht
M
Eingang
10.01.2023
Impfdatum
10.01.2022
Beginn
04.06.2022
Tage bis Beginn
145,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Acute kidney injury Acute respiratory failure Anaemia of chronic disease COVID-19 Cardiac failure Chronic kidney disease Condition aggravated Dyspnoea Hypertensive urgency Intensive care Pulmonary hypertension SARS-CoV-2 test positive

Symptomtext

Narrative: 71 y/o male w/ PMH for HTN, Asthma, HLD, Lumbago, CKD, and HF. Pt presented to the ED on 06/04/22 with SOB worsening over 5 days. Pt admitted to hospital ICU w/ acute hypoxic respiratory failure secondary to heart failure with reduced ejection fraction exacerbation. Pt also treated for Acute kidney injury on CKD 4, pulmonary hypertension, hypertensive urgency, anemia secondary to chronic disease and COVID-19 infection. Pt treated with dexamethasone (06/4-06/05) and supportive treatment during hospital stay for COVID. Pt improved and discharged to home on 06/14.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
-
Labordaten
06/04/2022- COVID 19 Positive
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2511323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

kritisch
Staat
FL
Alter
-
Geschlecht
F
Eingang
19.11.2022
Impfdatum
08.11.2022
Beginn
12.11.2022
Tage bis Beginn
4,0
Dosis
4
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Balance disorder Body temperature Cerebrovascular accident Dizziness Ear discomfort COVID-19 Drug ineffective SARS-CoV-2 test Ear pain Gait disturbance Head discomfort Headache Inappropriate schedule of product administration Pyrexia Vertigo

Symptomtext

Covid test result: Positive; Covid test result: Positive; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from product quality group. The reporter is the patient. A 61-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 08Nov2022 at 12:00 as dose 5 (booster), single (Lot number: GH9694), in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), as dose 4 (booster), single (Lot number: FJ5683), in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroid" (unspecified if ongoing). The patient took concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 12Nov2022, outcome "unknown" and all described as "Covid test result: Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (12Nov2022) Positive, notes: Nasal Swab. Course of events: No covid prior vaccination. No known allergies. No other vaccine in fourweeks. Patient got the Pfizer bivalent shot on noon 08Nov2022 at Pharmacy or Drug Store. She developed fever and headache the next day in the 38.5 C and pain and pressure in her ears like ear fullness felt like her ears inside will explode from pressure inside both ears. The second day the fever went away never came back, but she was dizzy and it got worse the third day Friday 11Nov2022 in the morning she had a severe dizzy spell and was resting all day but at 10 pm Friday 11Nov2022 she had severe vertigo lost ability to walk or stay on her feet so she was so scared she was having a stroke could not get up from lying position. She could not turn her head or move if she did it was scary like she was being moved violently like thrown away left or right totally lost coordination balance ability to walk and her ears and head were full under pressure even on 15Nov2022 day 7 she felt pressure. Saturday 7 am 11Nov2022 she called emergency to take her to the hospital manage on the floor to drag herself to open the door and they took me to Emergency.; Sender's Comments: Drug ineffective depends on many factors including pharmacokinetics, the pandemic and patient general health condition. However on conservative basis, the possible causality cannot be excluded.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebrovascular accident
Hospital-Tage
-
Labordaten
Test Date: 20221112; Test Name: PCR; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2489933

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

kritisch
Staat
TX
Alter
62,0
Geschlecht
M
Eingang
26.10.2022
Impfdatum
10.02.2022
Beginn
21.10.2022
Tage bis Beginn
253,0
Dosis
3
Route/Site
IM / AR
Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Atelectasis Blood creatinine Brain natriuretic peptide increased COVID-19 Computerised tomogram abdomen Computerised tomogram thorax abnormal Cough Death Dyspnoea Haematocrit Haemoglobin Lung consolidation Pleural effusion SARS-CoV-2 test positive Tachycardia Troponin normal White blood cell count

Symptomtext

Pfizer BioNTech COVID-19 Vaccine EUA: COVID-19 case resulting in Hospitalization/Death. Rec'd Pfizer BioNTech vaccine on 9/8/2021, 5/18/2021 and 2/10/2022. Presented to ED with c/o SOB and coughing. Pt was dx'ed w/covid-19 and admitted. Upon admission pt was tachycardic in 130s, sats 96% on 4L O2.BNP elevated 1700+, trops neg, creatinine, h/h, and wbc near baseline. CT ab pelv and chest: findings included large bilateral lower lung consolidations, atelectasis and small pleural effusions. Pt continued to decline despite treatment. Transitioned to comfort care and changed to DNAR/AND. Admitted to inpatient hospice service, expired 10/21/22. Tx'd w/decadron and rifaximin.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
3,0
Labordaten
Covid-19 + 10/19/22 - This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification(NAA)technology.
Aktuelle Erkrankungen
-
Vorgeschichte
EtOH cirrhosis, diastolic CHF, CKD4, obesity, anemia, BPH, Cancer, DM, HLD, CAD, HTN, Hypothyroidism, Cancer
Andere Medikamente
cephalexin, albuterol sulfate, calcium citrate/vitamin D3,
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2315844

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

kritisch
Staat
-
Alter
78,0
Geschlecht
F
Eingang
10.06.2022
Impfdatum
22.03.2022
Beginn
30.05.2022
Tage bis Beginn
69,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Acute respiratory failure COVID-19 Chronic obstructive pulmonary disease Condition aggravated Respiratory failure

Symptomtext

Acute exacerbation of chronic obstructive pulmonary disease triggered by COVID 19 causing an acute chronic hypoxemic respiratory failure. COVID-19 that lead to hospitalization. Patient was treated with a 3 day course of remdesivir and 5 days of prednisone.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acute respiratory failure
Hospital-Tage
4,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2197899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

kritisch
Staat
-
Alter
36,0
Geschlecht
F
Eingang
25.03.2022
Impfdatum
01.02.2022
Beginn
17.03.2022
Tage bis Beginn
44,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Exposure during pregnancy Foetal death

Symptomtext

Intrauterine fetal death discovered at 24 weeks and 3 days gestation. Infant girl delivered on March 24, 2022. This is patient's second pregnancy. First pregnancy was successful.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Foetal death
Hospital-Tage
3,0
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
none
Allergien
NKA
Vorherige Impfungen
-

VAERS 2155185

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

kritisch
Staat
CA
Alter
73,0
Geschlecht
M
Eingang
03.03.2022
Impfdatum
18.01.2022
Beginn
20.01.2022
Tage bis Beginn
2,0
Dosis
3
Route/Site
IM / LA
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Death

Symptomtext

death - reported to primary care provider today, March 3, 2022 as died on January 20, 2022. Do not know circumstances surrounding the death.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
unk
Aktuelle Erkrankungen
- Right hand problems s/p s/p Right carpal, cubital (in situ release) and ulnar tunnel release on August 13, 2021 - cervicalgia for several months - "too much gas when I eat" (and see below)
Vorgeschichte
Past Medical History/ACTIVE PROBLEMS: *Vitamin D Deficiency *Secondary myelofibrosis *Gout *COVID-19 on 1/9/21 that required hospitalization, supplemental O2, dexamethasone, and convalescent plasma. The pt. currently has persistent DOE. *Polycythemia vera *Myelodysplastic syndrome *Meralgia paresthetica *Obesity *Hypertension *Hyperlipidemia *Benign Localized Hyperplasia of Pro*Allergic rhinitis *Anemia --had BM biopsy 8/27/13, chronic Myeloproliferative disease had another bone marrow biopsy in April per dr *H/O cellulitis of left lower limb--June 2020 *Gastroesophageal Reflux Disorder *Osteoarthrosis involving the knee *CAVUS DEFORMITY OF FOOT *OSA *C-spine DDD *Vitamin D deff ***History of polyp of colon -Tubular adenoma; s/p colonoscopy 11/2013 SURGICAL HX: *Left hand surgery 1970s
Andere Medikamente
1) ALLOPURINOL 100MG TAB TAKE THREE TABLETS BY MOUTH ACTIVE EVERY DAY FOR GOUT -TAKE WITH A FULL GLASS OF WATER 2) ASPIRIN 81MG CHEW TAB CHEW ONE TABLET BY MOUTH EVERY ACTIVE DAY FOR STROKE/HEART ATTACK PREVENTION -
Allergien
No known drug allergies
Vorherige Impfungen
-

VAERS 2128000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

kritisch
Staat
CA
Alter
50,0
Geschlecht
F
Eingang
19.02.2022
Impfdatum
10.01.2022
Beginn
01.01.2022
Tage bis Beginn
-
Dosis
3
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Cerebrovascular accident Hypoaesthesia Pain in extremity Paraesthesia

Symptomtext

she thought she was having a stroke; numbness in the hand up to the elbow; shooting pain up the right foot.; her right foot experience tingling feeling in the toes and ankle; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 50 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 10Jan2022 (Lot number: FJ5683) at the age of 50 years as dose 3 (booster) , single for covid-19 immunisation. The patient had no relevant medical history. There were no other vaccines within four weeks prior to the first administration date of the suspect vaccine(s). There were no additional Vaccines Administered on Same Date of the Pfizer Suspect. There were no concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1. SINGLE, First Dose given on 20Jan2021: , Vaccine Lot Number: EL0142), administration date: 20Jan2021, when the patient was 49 years old, for covid-19 immunization, reaction(s): "she felt like she was in a car accident neck down and had to Crawl to the Comfort room that lasted 2 days", "she felt like she was in a car accident neck down and had to Crawl to the Comfort room that lasted 2 days", "but every bone and everything hurt for two days", "but every bone and everything hurt for two days"; Bnt162b2 (DOSE 2, SINGLE), administration date: 11Feb2021, when the patient was 49 years old, for COVID-19 Immunization, reaction(s): "extreme numbness on the left hand"; Tetanus, reaction(s): "never had any issues". The following information was reported: CEREBROVASCULAR ACCIDENT (medically significant), outcome "unknown", described as "she thought she was having a stroke"; HYPOAESTHESIA (non-serious), outcome "unknown", described as "numbness in the hand up to the elbow"; PARAESTHESIA (non-serious) with onset Jan2022, outcome "recovered", described as "her right foot experience tingling feeling in the toes and ankle"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "shooting pain up the right foot.". Clinical course: After she got the booster shot on 10Jan2022, the numbness has gotten worse. It starts with the left hand being completely numb than then goes up to her elbow. It can last for 2 hours, and it's not like she slept poorly. She massages her arm and hand. She thought she was having a stroke on left side. On the right side her foot starts having a tingling sensation with shooting pain up the right foot. Her right foot experienced tingling feeling in the toes and ankle but it went away and it's better now. This really scared her, that happened just a few days ago. She did not go to the doctor for the reported events, but now it has gotten so serious, she is having to take time out of her life and pay for a neurologist to check this out due to the severity of her symptoms. She feels like her left side has gone lame, she can still use it but she is concerned about using her left hand at all if it gets worse. She stated this is very concerning she might lose complete ability in her left hand and arm.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200221732 Same patient/ similar drug, different AE in seperate time gap;US-PFIZER INC-202200222074 Same patient/ similar drug, different AE in seperate time gap

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cerebrovascular accident
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2059005

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

kritisch
Staat
MN
Alter
37,0
Geschlecht
M
Eingang
24.01.2022
Impfdatum
14.01.2022
Beginn
19.01.2022
Tage bis Beginn
5,0
Dosis
3
Route/Site
IM / AR
Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Autopsy Death Decreased appetite Dyspnoea Headache Heart rate increased Hypophagia Insomnia Laboratory test Pyrexia Vomiting

Symptomtext

Patient received his booster shot on 1/14/22. On the evening of 1/14/22 he got a massive fever, loss of appetite, and inability to sleep. On 1/15/22 he had a lingering headache and continued loss of appetite, but he forced himself to eat. He started vomiting on 1/16/22 and said he was constantly vomiting from 12:00 a.m. - 5:00 p.m.. He estimated he vomited 8 times, until there was literally nothing left. He said he didn't really eat anything or get good sleep on 1/16/22. On 1/17/22 he reported he had shortness of breath and noted his heart was beating "quite fast." He noted that when he cooled his head it helped the shortness of breath "a lot." His last communication was at 8:40 p.m. on 1/17/22. He was scheduled to teach a virtual class at the local College on 1/18/22, he did not attend. He was found deceased in his apartment on 1/20/22 at 8:00 am.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Death
Hospital-Tage
-
Labordaten
Patient was taken to the Medical Examiner on 1/20/22. An autopsy was performed by the ME and there was no preliminary cause of death noted. The ME sent several tissue samples out for third party testing. We were told that he was deceased by 8:00 a.m. on 1/19/22.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Soylent
Allergien
-
Vorherige Impfungen
-

VAERS 2550927

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
PA
Alter
18,0
Geschlecht
F
Eingang
05.01.2023
Impfdatum
11.01.2022
Beginn
01.01.2022
Tage bis Beginn
-
Dosis
3
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Electrocardiogram Electroencephalogram Heart rate Heart rate increased Menstrual disorder Seizure Weight Weight decreased

Symptomtext

seizures; rapid heart beats; losing your menstrual cycle for months/lost cycle 5 months; Lost a lot of weight; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 19-year-old female patient received BNT162b2 (BNT162B2), on 11Jan2022 as dose 3 (booster), single (Lot number: FJ5683) at the age of 18 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (unspecified if ongoing), notes: Had high blood pressure, was high every time she went to doctor. The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (dose 1, single, LOT: EW0151, NDC EXP: Unknown, Anatomical location : Left arm), administration date: 20Apr2021, when the patient was 18-year-old, for Covid-19 immunization; BNT162b2 (dose 2, single, LOT: EW0173, NDC EXP: Unknown, Anatomical location :Left arm), administration date: 11May2021, when the patient was 18-year-old, for Covid-19 immunization; flu (had flu shot 14Oct2021, nurse said do not get flu shot), administration date: 14Oct2021, when the patient was 18-year-old, for covid-19 immunization. The following information was reported: HEART RATE INCREASED (hospitalization, medically significant) with onset Jan2022, outcome "unknown", described as "rapid heart beats"; MENSTRUAL DISORDER (non-serious) with onset May2022, outcome "unknown", described as "losing your menstrual cycle for months/lost cycle 5 months"; SEIZURE (hospitalization, medically significant) with onset May2022, outcome "not recovered", described as "seizures"; WEIGHT DECREASED (non-serious) with onset 2022, outcome "unknown", described as "Lost a lot of weight". The patient was hospitalized for heart rate increased, seizure (start date: 15Aug2022, discharge date: 16Aug2022, hospitalization duration: 2 day(s)). The events "rapid heart beats", "seizures", "losing your menstrual cycle for months/lost cycle 5 months" and "lost a lot of weight" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Electrocardiogram: (Jan2022) rapid heart beat, told her it was probably just i, notes: side effect; Electroencephalogram: (15Aug2022) Unknown Results, notes: they could not find anything conclusive to say it was or wasn't seizures. She was admitted to hospital overnight for EEG on 15Aug2022; Heart rate: (May2022) rapid heart beats; Weight: (unspecified date) 106, notes: Weight: Was 108, is now 106 right now. She was 120 something; (unspecified date) 120, notes: Weight: Was 108, is now 106 right now. She was 120 something; (unspecified date) 108, notes: Weight: Was 108, is now 106 right now. She was 120 something; (May2022) 117, notes: Thinks maybe she was 117 in May2022. Therapeutic measures were taken as a result of menstrual disorder. Clinical course: Indication for Use of vaccine in Case was reported as didn't want to catch Covid. No other conditions. Patient did not get any vaccinations within 6 weeks of Covid booster shot. No Family Medical History Relevant to Adverse Events. Patient had 2 Pfizer shots and the Pfizer booster; With the first 2 shots, didn't have any problems. Then they came out and said to take the booster 3 months after the first ones. After that, is not taking anymore. Took booster to go back to school, was college student and had to take it. Concomitant Products/Medical Conditions included had high blood pressure, was high every time she went to doctor. They would say it was white coat syndrome (patient did not think it was that). Thinks it was high before she got Covid. Does not know if something triggered her blood pressure but she always had high blood pressure. Was finally diagnosed from the cardiologist. Thinks she had high blood pressure before the booster but was not diagnosed with high blood pressure until after that. Had been dealing with that since eight grade. Thinks the booster, is what messed her up. Before that, she was fine. Thinks she had Covid before getting the shots, before they knew what Covid was. Shortly after booster, began to have rapid heart beats which was known as a side effect. Patient went to emergency room 14Jan2022, 3 days after booster. Went to emergency room with rapid heart beat. They checked her, did EKG, told her it was probably just side effect. Clarified that she was admitted to hospital overnight for EEG on 15Aug2022. When she kept having episodes on the EEG, they could not find anything conclusive to say it was or wasn't seizures. When having episodes, they took her to emergency room and they had her stay one night to for the EEG. Will have the ambulatory EEG 10Jan2023. The neurologist wants to see if they can capture anything with the episodes she is having and see if they look like seizures. Patient was having seizure like episodes, almost like freezing and they are not like tonic-clonic or those seizures that where they shake but these were seizure like episodes. Lost a lot of weight after the Pfizer shot. Are these side effects that a lot of people are reporting. The seizures, she thinks she has seen that but losing her cycle. Patient would like to know if seizures and losing menstrual cycle for months are symptoms other people have reported after having the booster. There's a lot of articles where they mention that the women cycles disappear. Is in the process of changing to different doctor but current doctor will have all of her records. Kept reporting this to the doctors but they kept dismissing it, when her cycle stopped. Started searching it and seeing that other people were experiencing it. Talked to the doctor today and they told her to maybe report it to Pfizer. Nobody had that before. Seizures, Also started May2022. Is still experiencing them now. Is scheduled for 72 hour ambulatory EEG, 10Jan2023. Is going to neurologist and they want to make sure there is nothing going on with the brain. Has not experienced anything like this until she took the Pfizer booster. Outcome of event was it has gotten worse. Is now starting to urinate on herself and has to wear pads. Clarified that this only occurs when she is having seizures. Is going back to see the neurologist. Weight loss, first noticed, she thinks, maybe in May or Jun2022. Thinks maybe she was 117 in May2022 then, all of a sudden, started dropping, almost monthly. Before that, had healthy appetite, couldn't eat right after booster. With all her heart problems she experienced from the booster, her primary care physician sent her to the cardiologist. Nothing was wrong with her heart and they were doing all this stuff for her heart. Lost cycle 5 months, Didn't have any cycles from May2022 until Nov2022. Saw a specialist and they put her on this medicine that made her cycle come back. Only took it 3 days and it was making heart hurt and chest hurt. Took that and cycle came back on, so it did work. Clarified that the medicine previously mentioned that she cause the chest pain was like a low dose birth control pill, to get her cycle to come back. The gynecologist gave her that name of that medication provided as Norethindrone. It made her chest hurt. Went back to gynecologist and they told her not to take it. Her cycle came on 3 days later. Lost her cycle for 5 months. It finally came back but now.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
2,0
Labordaten
Test Date: 202201; Test Name: EKG; Result Unstructured Data: Test Result:rapid heart beat, told her it was probably just i; Comments: side effect.; Test Date: 20220815; Test Name: EEG; Result Unstructured Data: Test Result:Unknown Results; Comments: they could not find anything conclusive to say it was or wasn't seizures. She was admitted to hospital overnight for EEG on 15Aug2022.; Test Date: 202205; Test Name: heart beat; Result Unstructured Data: Test Result:rapid heart beats; Test Name: Weight; Result Unstructured Data: Test Result:106; Comments: Weight: Was 108, is now 106 right now. She was 120 something; Test Name: Weight; Result Unstructured Data: Test Result:120; Comments: Weight: Was 108, is now 106 right now. She was 120 something; Test Name: Weight; Result Unstructured Data: Test Result:108; Comments: Weight: Was 108, is now 106 right now. She was 120 something; Test Date: 202205; Test Name: Weight; Result Unstructured Data: Test Result:117; Comments: Thinks maybe she was 117 in May2022
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Blood pressure high (Had high blood pressure, was high every time she went to doctor.)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2514615

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
GA
Alter
20,0
Geschlecht
F
Eingang
22.11.2022
Impfdatum
21.01.2022
Beginn
21.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein
Abdominal pain Activated partial thromboplastin time abnormal Arthralgia Aura Blindness unilateral Blood test abnormal Chest pain Constipation Dizziness Dysarthria Echocardiogram abnormal Electric shock sensation Electrocardiogram abnormal Electrocardiogram ambulatory abnormal Epistaxis Facial paralysis Fatigue Haemorrhagic disorder

Symptomtext

The night of the vaccine (1/21/22), I had a strong sensation of pins and needles throughout the whole left arm and hand. The following day, my arm began to feel numb and weak as well. The pins and needles, diminished sensation and weakness is still present to this day (11/22/22). Also, if I put too much pressure on the hand, like weight-lifting, there will be a shock that travels through my whole arm and I lose the function of that arm for a couple of minutes. On 5/4/22, I was working out at the gym and while I was doing cardio, I began to lose vision in my right eye. Everything became dark and tunnel vision and then I had a major headache. I started to see an aura and then lost feeling on the whole left side of my body. Then my face began to droop and I was slurring my words. I then began to have chest pain and was lightheaded and dizzy. I then went to the emergency department the following day (5/5/2022) where they found PVC's on my EKG and referred me to a neurologist and a cardiologist. I then went to see a cardiologist (5/12/22) and then did a work up and found multiple PVCs on multiple EKG's and a halter monitor and also took an echocardiogram of my heart and found mitral valve regurgitation. The chest pain did not subside and I ended up in the emergency the next day (5/13/22) Then the following months after this incident I constantly am suffering fatigue, joint and muscle pain, frequent urination, constipation, easy bruising, bloody noses, nausea, abdominal pain, night sweats, itchy skin. Had lab work done 11/4/22 and found a value out of normal which pointed to a type of bleeding disorder. Got bloodwork done again on 11/18/22 and still pending results. these symptoms are still present today 11/22/22.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Electric shock sensation
Hospital-Tage
-
Labordaten
PVC's found on EKG on 05/05/22 PVC's found on EKG and mitral regurgitation found on 05/12/22 PVC's found on 24 hour halter monitor 05/12/22 Abnormal bloodwork on 11/04/22 (aPPT and INR) suggests hemophillia
Aktuelle Erkrankungen
Covid at the end of December 2021
Vorgeschichte
None before vaccination
Andere Medikamente
Estarylla (birth control)
Allergien
None
Vorherige Impfungen
-

VAERS 2287256

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
MN
Alter
86,0
Geschlecht
F
Eingang
20.05.2022
Impfdatum
12.05.2022
Beginn
19.05.2022
Tage bis Beginn
7,0
Dosis
4
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 Intensive care Pneumonia SARS-CoV-2 test positive

Symptomtext

Received Pfizer vaccines on 1/27/21, 2/17/21, 10/21/21, 5/12/22; tested positive for COVID by PCR on 5/19/22; admitted to hospital ICU on 5/19/22 d/t pneumonia d/t COVID19. PMH of COPD/asthma, heart failure, pulmonary HTN.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Intensive care
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2225315

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

schwer
Staat
NY
Alter
20,0
Geschlecht
F
Eingang
09.04.2022
Impfdatum
09.04.2022
Beginn
09.04.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Dizziness Pallor Syncope

Symptomtext

post vaccine client fainted did not hit head, skin pale (history of fainting), light headed. Client awake and talking lay down with feet elevated, water and OJ given. No improvement offer to call 911 sent to ER

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2200727

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

schwer
Staat
WA
Alter
22,0
Geschlecht
M
Eingang
26.03.2022
Impfdatum
26.03.2022
Beginn
26.03.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Fall Head injury Loss of consciousness Muscle rigidity

Symptomtext

Administered vaccine, Patient asked for some water, left to go get some, heard a noise, called patient's name and received no response, came back into room to patient going rigid and falling to floor hitting his head on the cabinet on the way down. I instructed my technician to dial 911 for medics. Patient was unconscious briefly and required medical assistance and brief hospitalization in E.D.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
Blood pressure monitoring. Unknown tests at E.D.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Unknown
Allergien
None
Vorherige Impfungen
unknown, patient stated when about 18 years of age

VAERS 2179937

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

schwer
Staat
TX
Alter
30,0
Geschlecht
M
Eingang
15.03.2022
Impfdatum
15.03.2022
Beginn
15.03.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Dyspnoea Electrocardiogram Hyperhidrosis Seizure

Symptomtext

after 6 min of vaccine pt started sweating and convulsion was noted for about 1 min. then pt had sob.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
ekg was performed
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
no
Vorherige Impfungen
-

VAERS 2179770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

schwer
Staat
TX
Alter
16,0
Geschlecht
M
Eingang
15.03.2022
Impfdatum
14.03.2022
Beginn
14.03.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Syncope

Symptomtext

Patient was dizzy and lightheaded, fainted but did not lose consciousness. Vitals normal.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2171052

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
MI
Alter
58,0
Geschlecht
F
Eingang
10.03.2022
Impfdatum
11.01.2022
Beginn
11.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Condition aggravated Fatigue Headache Immediate post-injection reaction Neurological symptom Seizure

Symptomtext

Patient had seizure or seizure-like activity immediately following vaccination; resolved without issue. RN on the Immunization team administered the Pfizer COVID-19 vaccine Booster to the pt. today and at the end of the 15 min. observation period RN noticed the pt. appeared fatigued and experienced seizure like activity. After the seizure subsided RN took vitals which were Within Normal Range. The pt. complained of fatigue and a headache. RN recommended calling 911 but the pt. refused, stating she has a seizure disorder and has had this happen in the past. Pt. denied having seizure activity with her two previous vaccine doses. RN told pt. and caregiver to call 911 if she developed new/worsening symptoms and then left the home.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
-
Vorgeschichte
Thyroid nodule Chronic pain Chronic pain syndrome Active smoker Right shoulder pain Adhesive capsulitis of right shoulder Preoperative cardiovascular examination Other convulsions Snoring Insomnia Restrictive lung disease secondary to obesity OSA (obstructive sleep apnea) Essential hypertension Type 2 diabetes mellitus with hyperglycemia, with long-term current use of insulin (HCC) Morbid obesity with body mass index (BMI) of 50.0 to 59.9 in adult (HCC) Primary osteoarthritis of right hip Osteoarthritis of spine with radiculopathy, lumbar region Psychogenic nonepileptic seizure Mixed hyperlipidemia Other dysphagia Hepatitis C Gastroesophageal reflux disease Epigastric pain Acute pancreatitis without infection or necrosis Axillary abscess Unspecified severe protein-calorie malnutrition (HCC) Idiopathic acute pancreatitis without infection or necrosis Skin tag Intertriginous candidiasis Adrenal nodule (HCC)
Andere Medikamente
albuterol (PROVENTIL, VENTOLIN, PROAIR) 108 (90 Base) MCG/ACT inhaler amLODIPine (NORVASC) 5 MG tablet aspirin 81 MG enteric coated tablet buPROPion (WELLBUTRIN XL) 300 MG 24 hr tablet buPROPion HCl ER, XL, 450 MG 24 hr tablet dicyclomine (
Allergien
BeeAnaphylaxis Botox [Albumin] DoxycyclineNausea and Vomiting Lyrica [Pregabalin]Dizziness Onabotulinumtoxina Vitamin C [Ascorbate]Nausea and Vomiting
Vorherige Impfungen
-

VAERS 2166264

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
CA
Alter
24,0
Geschlecht
M
Eingang
08.03.2022
Impfdatum
14.02.2022
Beginn
16.02.2022
Tage bis Beginn
2,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Arrhythmia Heart rate abnormal Pericarditis

Symptomtext

Pericarditis. Abnormal heartbeat, arrhythmia.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pericarditis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
n/a
Vorherige Impfungen
-

VAERS 2151587

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

schwer
Staat
PA
Alter
22,0
Geschlecht
F
Eingang
02.03.2022
Impfdatum
01.03.2022
Beginn
01.03.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Headache Syncope

Symptomtext

fainting shortly after immunization. Fainting resolved, pt reported headache next day.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2132239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
VA
Alter
42,0
Geschlecht
M
Eingang
22.02.2022
Impfdatum
12.01.2022
Beginn
12.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood iron decreased Blood thyroid stimulating hormone decreased C-reactive protein increased Chills Culture throat positive Goitre Haematocrit decreased Haemoglobin decreased Insomnia Iron binding capacity total decreased Mean cell haemoglobin decreased Mean cell volume decreased Pyrexia Red blood cell sedimentation rate increased Sensation of foreign body Serum ferritin increased Streptococcus test Syncope

Symptomtext

Covid Booster shot (3rd shot of Pfizer) was administered on 12-Jan-2022. I started noticing a lump on the left throat after vaccination I had extreme reactions to the booster shot including fever, chills and an episode of fainting. From then on, i started having fever every day (reaching high temperatures in the evening). I had trouble sleeping and sensitivity to cold. The throat lump started aching on the right side. I consulted my primary care physician on 30-Jan-2022 Throat culture came back positive, and the doctor put me on Penicillin 500 mg 3 times a day for 10 days I was also taking Tylenol especially in the evenings when the fever became high After 10 days, the fever subsided An ultrasound scan of the thyroid revealed that the right side is larger than the left side. No nodules were found. I was maintaining a weight of 140 LBs for several months, but since Jan-2022 until now, I have dropped to 120 Lbs My doctor has recommended consulting a Endocrinologist for further treatment My doctor has also recommended taking Propranolol 20 mg tablets 3 times a day

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
Low Hemoglobin (12.3 g/DL) Low Hematocrit (37.4%) Low MCV (73 fl) Low MCH (23.9 pg) Low TSH (0.006 uIU/mL) High Sedimentation rate-Westergren (58 mm/hr) Abnormal Beta Strep Gp A Culture High C-reactive protein, Quant (45 mg/L) Low Iron Bind.Cap.(TIBC) (249 ug/dL) Low Iron (37 ug/dL) High T4, Free(Direct) - (6.53 ng/dL) High Ferritin (466 ng/mL) High T3, Free (8.0 pg/mL) Ultrasound scan results - Right Thyroid lobe is larger in size compared to the left, no discrete nodules found
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Seafood
Vorherige Impfungen
-

VAERS 2131336

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
TX
Alter
37,0
Geschlecht
F
Eingang
22.02.2022
Impfdatum
22.02.2022
Beginn
22.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest pain Seizure Unresponsive to stimuli

Symptomtext

Pt received vaccine, pt was c/o chest pain @ 1050. Requested PAR to call rapid response team, pt started to be unresponsive and requested PAR assistance to assisst pt to the floor. Rapid response team arrive @ 1051, pt place on Oxygen 2 lpm. EMS contacted, pt had 4 seizure episodes 1st was @ 1053 with 20 sec duration, 2nd @ 1056 with 46 sec duration, 3rd @ 1100 with 30 sec duration, 4th with @ 1107 lasted 20 sec. EMS arrive @ 1102 and left with pt @ 1110, pt referred to ED.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
Lupus History of blood clots Pulmonary embolism
Vorgeschichte
Lupus History of blood clots Pulmonary embolism
Andere Medikamente
N/A
Allergien
Benadryl [Diphenhydramine Hcl]Other (See Comments) Paxil [Paroxetine Hcl]Hives, Shortness Of Breath PromethazineOther (See Comments) Venom-honey BeeAnaphylaxis Adhesive Tape-siliconesItching DiphenhydramineOther (See Comments) GlutenOther (See Comments) Promethazine HclOther (See Comments) Propofol AnaloguesOther (See Comments)
Vorherige Impfungen
-

VAERS 2130086

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
PA
Alter
15,0
Geschlecht
F
Eingang
21.02.2022
Impfdatum
21.02.2022
Beginn
21.02.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Adverse event Dizziness Hypotension Pallor Syncope

Symptomtext

Approximately 5 minutes after the vaccination, patient experienced syncope (lightheadedness, low blood pressure, pale and fainting). Her father requested emergency medical services. EMS arrived, and evaluated her blood pressure, heart rate, and blood sugar (all within normal limits). They determined patient was safe to return home. Total time of adverse event thru evaluation (5:15 pm to 5:45 pm).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
Blood pressure, heart rate and blood sugar (all within normal limits on 2/21/2022; roughly 5:35 pm).
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2128560

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

schwer
Staat
WA
Alter
18,0
Geschlecht
M
Eingang
20.02.2022
Impfdatum
20.02.2022
Beginn
20.02.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Loss of consciousness Yellow skin

Symptomtext

patient got the vaccine and less than a minute later he slumped in his chair, his color was yellow HR was 38 BPM, emergency department were called he stayed unconscious for around 1 minute, patient claims that he has had anything to eat since breakfast and he claims that this has happened on his first dose, the ED waited till he is better and he walked to his parent car and went home according to mom

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
Pfizer 05/20/2021

VAERS 2123418

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
TN
Alter
34,0
Geschlecht
M
Eingang
18.02.2022
Impfdatum
16.02.2022
Beginn
16.02.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
Asthenia Chills Confusional state Disorientation Dizziness Dysphonia Face injury Fall Fatigue Incontinence Loss of consciousness Myalgia Nausea Oropharyngeal pain Photosensitivity reaction Pyrexia Restlessness Syncope

Symptomtext

Patient temporarily for work. Patient received COVID vaccine booster dose 2/16/22 around 1400. Afterwards, patient ate a meal then returned to hotel room. Around 2300, patient was tired and attempted to sleep, but felt restless, dizzy and nauseated, with sore/ hoarse throat and subjective feeling of chill/ fever. On 2/17, between 0230 and 0430, he attempted to get out of bed to use the bathroom when "everything went black." Patient stated he fell in the bathroom and when he woke up he had voided. Patient said when he came to he was confused and disoriented and at the time was very weak with myalgia. Patient promptly crawled back to the bed. He reported that he had fallen on his left side with the left side of his face striking the floor. Around 0900, the patient called his wife to give an update how he was feeling, and then called 911 and EMS arrived to his hotel room. Upon their evaluation of the patient they went to stand the patient and he had a second syncopal episode. The patient said he again blacked out and when he came to there were a number of people standing around him. After the fall, the patient does complain about photosensitivity and feeling of dizziness with turning of his head left or right. If he turns his head to either direction in a quick manner he feels like he is trying to catch up with his head when is actually stopped. He may have some component of post-concussion syndrome and/or benign positional paroxysmal vertigo secondary to the fall.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
1,0
Labordaten
-
Aktuelle Erkrankungen
None known
Vorgeschichte
anxiety, insulin-dependent diabetes mellitus and chronic pancreatitis, h/o splenectomy and pancreatectomy @ age 12
Andere Medikamente
alprazolam; insulin aspart, insulin glargine and methylphenidate
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2109074

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
MI
Alter
71,0
Geschlecht
F
Eingang
12.02.2022
Impfdatum
18.01.2022
Beginn
28.01.2022
Tage bis Beginn
10,0
Dosis
3
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Bell's palsy Chest X-ray Computerised tomogram head Facial paralysis Investigation SARS-CoV-2 test

Symptomtext

Diagnosed with bell palsy; left side of face drooping; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administration date 18Jan2022 12:00 (Lot number: FJ5683) at the age of 71 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Diabetes" (unspecified if ongoing); "Penicillin allergy" (unspecified if ongoing). The patient's concomitant medications were not reported. No other vaccine in four weeks. Vaccination history included: Bnt162b2 (Dose 2, Batch/Lot No: FJ5683, Arm Left, 12:00 PM), administration date: 18Jan2022, when the patient was 70 years old, for COVID-19 immunization; Bnt162b2 (Dose 1, Batch/Lot No: EM9809, Arm Left, 12:00 PM), administration date: 16Apr2021, when the patient was 70 years old, for COVID-19 immunization. The following information was reported: BELL'S PALSY (medically significant) with onset 28Jan2022 15:15, outcome "not recovered", described as "Diagnosed with bell palsy"; FACIAL PARALYSIS (medically significant) with onset 28Jan2022 15:15, outcome "not recovered", described as "left side of face drooping". The events "diagnosed with bell palsy" and "left side of face drooping" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: chest x-ray: (unspecified date) unknown results; computerised tomogram head: (unspecified date) unknown results; investigation: (31Jan2022) unknown results; sars-cov-2 test: (31Dec2021) negative, notes: Nasal Swab. Therapeutic measures were taken as a result of bell's palsy, facial paralysis.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bell's palsy
Hospital-Tage
-
Labordaten
Test Name: chests x-ray; Result Unstructured Data: Test Result:Unknown results; Test Name: CT head exam; Result Unstructured Data: Test Result:Unknown results; Test Date: 20220131; Test Name: bell palsy; Result Unstructured Data: Test Result:Unknown results; Test Date: 20211231; Test Name: SARS-COV-2 RT-PCR; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Diabetes; Penicillin allergy
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2108982

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
TX
Alter
13,0
Geschlecht
M
Eingang
12.02.2022
Impfdatum
25.01.2022
Beginn
25.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blindness Dizziness Syncope Tremor

Symptomtext

He began to say that he did not see; Fainted; Dizzy; Tremble; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 13 year-old male patient received bnt162b2 (BNT162B2), administered in arm left, administration date 25Jan2022 15:00 (Lot number: FJ5683) at the age of 13 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Asma bronchial" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose 2, Batch/Lot No: FC3181, Arm Left, Vaccine Administration Time: 01:00 AM), administration date: 25Aug2021, when the patient was 12 years old, for COVID-19 immunization; Bnt162b2 (Dose 1, Batch/Lot No: FA7485, Arm Left, Vaccine Administration Time: 12:00 PM), administration date: 04Aug2021, when the patient was 12 years old, for COVID-19 immunization. The following information was reported: BLINDNESS (medically significant) with onset 25Jan2022 15:00, outcome "unknown", described as "He began to say that he did not see"; SYNCOPE (medically significant) with onset 25Jan2022 15:00, outcome "recovered" (25Jan2022), described as "Fainted"; DIZZINESS (non-serious) with onset 25Jan2022 15:00, outcome "unknown", described as "Dizzy"; TREMOR (non-serious) with onset 25Jan2022 15:00, outcome "unknown", described as "Tremble". Patient began to say that he did not see, and dizzy to go to the side tremble and fainted for seconds. The events "he began to say that he did not see", "fainted", "dizzy" and "tremble" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of blindness, syncope, dizziness, tremor.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Asthma bronchial
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2102523

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
NY
Alter
19,0
Geschlecht
F
Eingang
10.02.2022
Impfdatum
10.02.2022
Beginn
10.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Cold sweat Pallor Presyncope

Symptomtext

After 3 minutes post injection, pt experienced vasovagal, no LOC, no head trauma, clammy Pale, EMS at site, Legs elevated to 45 degrees, no further episode. vs 101/67, Hr 67, o2 Sat 99 . R 18. in no respiratory distress, no chest pain. Pt observed and hydrated. Dr and EMS personnel with patient. Second VS Stable BP 117/75, HR 68 RR 20 SaO2 98 RA.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Presyncope
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
patient reports previous dizziness and lightheaded to previous vaccines and blood work

VAERS 2101780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

schwer
Staat
CA
Alter
18,0
Geschlecht
F
Eingang
10.02.2022
Impfdatum
08.02.2022
Beginn
08.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Seizure

Symptomtext

Pt was given first shot of Pfizer Covid 19 shot. Pt was instructed to stay 15 minutes for observation, After 10 minutes, pt had a seizure that lasted approximately 10 seconds. 911 was called . Pt was evaluated and taken to hospital and was discharged the same day. Follow up was done the next day via phone call. Pt stated she was fine

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none reported on vars form
Vorgeschichte
none reported on vars form
Andere Medikamente
none reported on vars form
Allergien
none reported on vars form
Vorherige Impfungen
Pt stated that she experienced dizziness with a previous vaccination

VAERS 2095942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
CA
Alter
34,0
Geschlecht
F
Eingang
08.02.2022
Impfdatum
07.02.2022
Beginn
08.02.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Headache Hyperhidrosis Syncope Vomiting

Symptomtext

Patient called pharmacy around 12 noon on 02/08/2022 and informed that she had adverse effects with her booster Pfizer vaccine around 2am today. she had fainted 2 times, sweating, dizzy, headache and vomiting. Advising patient to go to emergency department to check up and let her primary care doctor aware of this situation.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
not available yet.
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
NONE
Allergien
NONE
Vorherige Impfungen
-

VAERS 2092692

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
PA
Alter
21,0
Geschlecht
M
Eingang
07.02.2022
Impfdatum
04.02.2022
Beginn
04.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Hypotension Loss of consciousness Nausea Pallor

Symptomtext

Patient felt very nauseated, became pale, and passed out for a few seconds. Blood pressure was low initially. Patient was laid down flat, cool compresses applied, juice and crackers given to patient, vitals checked x 2. Patient monitored for 30-40 minutes afterwards.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
House Dust
Vorherige Impfungen
-

VAERS 2086221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
CA
Alter
10,0
Geschlecht
F
Eingang
03.02.2022
Impfdatum
03.02.2022
Beginn
03.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness postural Pallor Syncope

Symptomtext

Patient felt dizzy standing up and had brief syncope. She did not lose consciousness. Mother caught her in her arms and no injuries occurred. She looked pale and needed about 10-15 minutes before getting up and dizziness subsided. Pulse oximetry, BP, HR checked with no significant findings. Patient was advised to wait 30 minutes for observation, instructed to hydrate, inform guardian of any worsening symptoms and follow up with HCP.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
n/a
Allergien
none
Vorherige Impfungen
-

VAERS 2080064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
CA
Alter
23,0
Geschlecht
M
Eingang
01.02.2022
Impfdatum
01.02.2022
Beginn
01.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Seizure like phenomena

Symptomtext

About 3 minutes after getting the shot, patient presented with seizure-like reaction but immediately recovered ( less than a minute ). However he did not recognize his whereabouts but was able to realize it in a few seconds. Initial blood pressure taken was 77/53 , pulse 72 . We were calling 911 but he refused . Patient was awake , alert when he left the facility.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Seizure like phenomena
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Per patient not taking any medications
Allergien
Zithromax
Vorherige Impfungen
Johnson and Johnson covid vaccine

VAERS 2074670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
CA
Alter
15,0
Geschlecht
F
Eingang
29.01.2022
Impfdatum
29.01.2022
Beginn
29.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Hyperhidrosis Syncope Visual impairment

Symptomtext

Patient felt dizzy and fainted in moms lap in the observation area approximately 10-15 minutes post vaccination. States she felt lightheaded, diaphoretic and started seeing spots. Patient was out for a few seconds and was able to sit back up and take fluids. VS taken, BP 110/70 manual, HR 62 radial (40s initially on the digital pulse ox) , oxygen 98%, RR 18. Approx. Fluids and additional observation for 30 minutes. Patient improved and was able to ambulate to the car safely accompanied by myself and observation RN. Advised patient and mom to continue to rest, take plenty of fluids, and if symptoms return to go to urgent care or ER. Patient and mom verbalized understanding.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
-
Vorgeschichte
Grave's disease
Andere Medikamente
NA
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2059508

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
OH
Alter
12,0
Geschlecht
M
Eingang
24.01.2022
Impfdatum
24.01.2022
Beginn
24.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Fall Head injury Syncope

Symptomtext

patient experienced a syncopal episode about 15-20 minutes after receiving vaccine but did not seem to lose any consciousness, just fell to the floor; family members helped to brace his fall a little but think he did hit his head. EMS was called and blood pressure and blood sugar were checked and normal. Patient was anxious prior to vaccine and may not have eaten much prior to appointment. Family opted to have him taken to the hospital to be checked out just to be safe.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
unknown
Vorgeschichte
unknown
Andere Medikamente
unknown
Allergien
unknown
Vorherige Impfungen
-

VAERS 2057930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ 5683

schwer
Staat
OR
Alter
13,0
Geschlecht
M
Eingang
23.01.2022
Impfdatum
22.01.2022
Beginn
22.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fall Head injury Oedema Syncope

Symptomtext

Syncope Episode, Pt fell and hit right side of head, when i arrived at pts side he was conscious and breathing normally laying on his left side, i did my normal assessments and a neuro and trauma assessment, pt had an Edema on his head No lacerations or penatrations and his vitals were within normal range for his age, pts pupils were equal and reactive, Pts first set of vitals at 12:30 were Bp 125/80 p 61 rr 17 second set of vitals 12:36 Bp 120/75 P58 rr15 Pt was advised that emergency should be called but parent of pt refused emergency service I also advised parent of pt that pt should get his sons head checked by a doctor and parent acknowledged what i had said, Pt recovered and sat in room for another 30 min after 30minutes pt left with parent without incident

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
NKA
Vorherige Impfungen
-

VAERS 2032896

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
NJ
Alter
15,0
Geschlecht
F
Eingang
13.01.2022
Impfdatum
13.01.2022
Beginn
13.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Condition aggravated Dizziness Syncope

Symptomtext

Client became dizzy and fainted in monitoring area after vaccination. Vital signs 80/54, 85, 14. EMS dispatched to site however patient fully recovered and declined going to ER for evaluation.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
history of fainting and anxiety
Vorgeschichte
none
Andere Medikamente
none
Allergien
nka
Vorherige Impfungen
-

VAERS 2028679

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
PR
Alter
14,0
Geschlecht
F
Eingang
12.01.2022
Impfdatum
12.01.2022
Beginn
12.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Syncope

Symptomtext

A 14 year old female faints approximately 3 minutes after the vaccine is administered. The patient was evaluated, vital signs B/P 70/50, pulse 86, Resp. 16, Dextro 96mg/dl. Doctor is consulted, who indicates that she is placed on a stretcher with raised legs, oral fluids are replenished with "GATORADE" and that in 30 minutes vitals be re evaluated. At 30 min vitals are reassessed B/P 100/60, Pulse 96, Res 18, patient reports feeling well and without discomfort. To which doctor is consulted and indicates that he can withdraw from the vaccination center. Patient leaves walking on own feet.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Syncope
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Father of minor refers none.
Vorgeschichte
None
Andere Medikamente
Father of minor refers that patient does not take any medication for daily use.
Allergien
Father of minor refers not to have allergies to any food medications or vaccines.
Vorherige Impfungen
-

VAERS 2026103

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
OR
Alter
41,0
Geschlecht
F
Eingang
11.01.2022
Impfdatum
11.01.2022
Beginn
11.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Confusional state Cyanosis Dizziness Fatigue Loss of consciousness Pallor

Symptomtext

01/11/2022 @ drive though site On-site medic at the time in incident. Responded to 41 yr. old female w/ CC of "confusion. dizziness, and tired." Driver of the vehicle reports that the patient past out in the car w/ LOC before parking the car. Pt denies headache, dizziness, blurred vision, vomiting, difficulty breathing, recreational drugs, or recent illness. Pt is able communicate and responds appropriately to questions. A/O X 4. V/S: RR-12, SAo2- 96, HR-54, BP-120/60, CTM- pale, cool. and dry. Cap refill- <2 seconds PMH: Epilepsy, Rx Meds- Trazadone, Allergies- NKDA, last oral intake was yesterday. Physical Assessment- airway patent, breathing regular/slow/shallow/and without effort. Circulation- skin: cyanotic, warm, dry, pale. Pule- radial, slow, regular, weak Ambulance arrived at 1304. Patient placed in trendelenburg in passenger seat. Vitals reassess and within normal limits. EMS conducted by Site Lead-to paramedic- for follow on care to higher eschelon.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
N/A
Vorgeschichte
Epilepsy
Andere Medikamente
Trazodone
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2025724

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

schwer
Staat
-
Alter
17,0
Geschlecht
M
Eingang
11.01.2022
Impfdatum
11.01.2022
Beginn
11.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Loss of consciousness

Symptomtext

15 min post vaccine, patient passed out, assisted to ground by father, loc for 10-15 seconds. Assisted to gurney via wheelchair, BP 108/62, A&ox4, drank 8ox of water and 6ox of apple juice. Released to father,

Weitere VAERSDATA-Felder
Praegender Schweregrund
Loss of consciousness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Autistic
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2709797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
TN
Alter
28,0
Geschlecht
F
Eingang
03.11.2023
Impfdatum
16.03.2021
Beginn
14.08.2023
Tage bis Beginn
881,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest pain Computerised tomogram Dizziness Dyspnoea Electrocardiogram Magnetic resonance imaging Tachycardia

Symptomtext

I've had a sudden onset of tachycardia, with dizziness, difficulty breathing, and pain in my chest. So far after going to the doctor, they have not been able to find the cause. It was at one of these appointments that I was talking to a nurse at let me know other women have been through with similar problems and it might be do to the vaccine. In the case that it is caused by the vaccine I wanted to report it in some way. From the experience I've had not be taken seriously about my symptoms, I could understand that it may be something that is under reported in women in particular.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
I've had Cat scans, EKG, MRI
Aktuelle Erkrankungen
-
Vorgeschichte
Chronic pain and nerve damage
Andere Medikamente
Zoloft
Allergien
Small allergy to mushrooms
Vorherige Impfungen
-

VAERS 2624411

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge FJ5683

moderat
Staat
AZ
Alter
40,0
Geschlecht
M
Eingang
01.05.2023
Impfdatum
11.01.2022
Beginn
01.07.2022
Tage bis Beginn
171,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein
Autoimmune disorder Blood test Brain oedema Brain stem syndrome CSF test Dysarthria Encephalitis brain stem Gait inability Hypoaesthesia Injection site pain Laboratory test Lethargy Loss of personal independence in daily activities Magnetic resonance imaging Motor dysfunction Musculoskeletal disorder Paraesthesia Positron emission tomogram

Symptomtext

Initially there was no reaction except soreness at the site. After about 6 weeks became lethargic which slowly increased over 6 months leading to numbness and tingling in hands, feet and slurring of speech. went to several emergency rooms only to be sent home. In July 2022 finally admitted to local Health Services with unknown diagnosis. Went to alternate Clinic where it was diagnosed as autoimmune rhombencephilitis and hospice was recommended. Lifeflighted to 2nd. alternate facility for stem cell transplant. Currently in inpatient rehabilitation . Cannot walk, cannot use arms for eating dressing or grasping objects. Speech remains difficult.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
There are too many to list. Had many spinal fluid tests, MRI, PET scan, xrays, blood testing from July 2022 to present to rule out infectious or viral disease. None found. Swelling of the brainstem and cerebellum.
Aktuelle Erkrankungen
None
Vorgeschichte
Since immunization, has developed Autoimmune Rhombencephalitis.
Andere Medikamente
Ibuprofen as needed
Allergien
None
Vorherige Impfungen
-

VAERS 2608400

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
VA
Alter
75,0
Geschlecht
F
Eingang
03.04.2023
Impfdatum
30.03.2022
Beginn
23.06.2022
Tage bis Beginn
85,0
Dosis
4
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Atrial fibrillation Cardiac ablation Cardiac monitoring abnormal Cardioversion Palpitations

Symptomtext

Heart palpitations, no pain, palpitations would not stop, my heart was 125 BPM. Basically that was something that happened to me that was new and it would not stop and it went until November 2022. I had shock treatment to the heart in the hospital but that did not work, a month later I had an ablation that got my heart rate under control.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
Stress monitor diagnosis was AFIB.
Aktuelle Erkrankungen
None
Vorgeschichte
Epilepsy; Diabetes; Hypertension
Andere Medikamente
Carbamazepine; KEPPRA; lacosamide; nifedipine; losartan; simvastatin; XANAX; lisinopril
Allergien
Sulfa
Vorherige Impfungen
-

VAERS 2560678

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
IL
Alter
35,0
Geschlecht
F
Eingang
16.01.2023
Impfdatum
10.02.2022
Beginn
11.02.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Amino acid level Antinuclear antibody Arthralgia Blood cortisol Blood homocysteine Blood iron Blood thyroid stimulating hormone C-reactive protein Cardiac disorder Discomfort Feeling abnormal Female sex hormone level Full blood count Impaired work ability Lipids Loss of personal independence in daily activities Metabolic function test Musculoskeletal stiffness

Symptomtext

The next morning on 2/11/21, I woke up and had extreme joint pain and body stiffness. I also had brain fog. I arrived to work at 8:00 am and left by 10:00 am because, I couldn't function. It hurt to move my body and I was so out of it I couldn't even type an email. I rested the entire weekend and continued to have brain fog that eventually lifted. I then noticed my body felt heavy and I felt like my heart couldn't calm down when lying down. I noticeably felt my heart beating when laying down. I also started to notice my tonsils were enlarged and I was squeezing stones out of them and also noticed my tounge was white and dry and still have this issue with my tounge today.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
CRP and ESR 6/15/22 Lipid Panel 6/15/22 TSH 04/06/22 Metabolic panel 4/6/22 CBC 4/6/22 Iron panel 4/6/22 Cortisol 4/6/22 Hormones 4/6/22 Vitamin B12 6/15/22 Homocysteine 7/6/22 Methylmalonic Acid 7/6/22 Vitamin B12 7/6/22 CBC 8/25/22 Rheumatoid Factor 8/25/22 Vitmain D 8/25/22 ESR 8/25/22 Anti nuclear Antibody 8/25/22 Thyroid Panel 11/10/22
Aktuelle Erkrankungen
Was diagnosed with Covid-19 on December 15th, 2021. Was told I could get the vaccine as soon as I was feeling better and after my isolation period per my doctor. Right before I got the vaccine on 2/10/21 at my appointment I asked the nurse if I needed to wait 90 days, because I just had covid-19. She said no, as long as I had not received the mono-clono antibodies then I was fine to get the vaccine.
Vorgeschichte
PCOS - poly cystic ovarian syndrome
Andere Medikamente
Metformin, spironolactone, tri-sprintec
Allergien
none
Vorherige Impfungen
-

VAERS 2557789

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
UT
Alter
72,0
Geschlecht
F
Eingang
11.01.2023
Impfdatum
10.01.2022
Beginn
01.02.2022
Tage bis Beginn
22,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Atrial fibrillation COVID-19 Dyspnoea Dyspnoea exertional Echocardiogram abnormal Electrocardiogram ambulatory Feeling abnormal Heart rate increased SARS-CoV-2 test positive

Symptomtext

I was short of breath. I felt different. I couldn't walk without running out of breath. My heart was beating really fast. In September is when everything really started to go wacko. September 22, 2022 that is usually high was very low. I just didn't feel good. I got on heart monitors and going to the doctor. They referred me to a cardiologist. I'm doing at home EKG monitoring at home. I have to check my weight, EKG daily. Went back into doctor in December.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
13DEC2022 Echocardiogram, Atrial Fibrillation; JAN2022 COVID-19 at home test positive
Aktuelle Erkrankungen
N/A
Vorgeschichte
High Blood Pressure; Environmental Allergies
Andere Medikamente
Pravastatin sodium; BYSTOLIC; BENICAR; clonidine HCL; glucosamine chondroitin; PREMARIN; multivitamin; montelukast sodium; mometasone furoate; garlic capsule; fish oil; vitamin C; vitamin D3; cinnamon capsule; fluoxetine HCL; diclofenac sod
Allergien
Erythromycin; gluten
Vorherige Impfungen
2nd Pneumonia shot a few years ago. It made me really sick

VAERS 2533677

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NY
Alter
69,0
Geschlecht
F
Eingang
16.12.2022
Impfdatum
24.01.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Bedridden Decreased appetite Mobility decreased

Symptomtext

She got at 8 am on a Sunday. At 5pm that same day, she couldn't move/ She just was unable to get out of bed for 2 days; She just was unable to get out of bed for 2 days.; She wasn't eating; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP), Program ID. The reporter is the patient. A 70-year-old female patient received BNT162b2 (BNT162B2), on 24Jan2022 as dose number unknown, (booster) single (Lot number: FJ5683) at the age of 69 years for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing); "Unreactive thyroid" (unspecified if ongoing); "Hot flashes" (unspecified if ongoing), notes: She had issues with hot flashes and had to go on hormone replacement; "Menopause" (unspecified if ongoing), notes: She had issues with hot flashes early and then when she started menopause they took her off everything and put her on Prempro.; "hormone replacement" (unspecified if ongoing), notes: She was put on a low dosage of birth control because of it which is hormone replacement.; "Sleep disorder" (unspecified if ongoing), notes: She is not able to sleep due to hot flashes. Concomitant medication(s) included: LOSARTAN taken for hypertension; FUROSEMIDE; LEVOTHYROXINE taken for thyroid disorder. Vaccination history included: BNT162b2 (She was fine after her first covid shot, First dose: 31Jan2021-EN5318), administration date: 31Jan2021, when the patient was 68-year-old, for COVID-19 immunization; BNT162b2 (Her second one three weeks later she got at 8 am on a Sunday. At 5pm that same day, she couldn't move., She had to lay down. She was so nauseous. , She was in bed for 3 days., She wasn't eating. She never vomited., Lot: EN6198), administration date: 21Feb2021, when the patient was 68-year-old, for COVID-19 immunization, reaction(s): "She got at 8 am on a Sunday. At 5pm that same day, she couldn't move", "She had to lay down. She was so nauseous", "She was in bed for 3 days", "She wasn't eating". The following information was reported: MOBILITY DECREASED (non-serious), outcome "unknown", described as "She got at 8 am on a Sunday. At 5pm that same day, she couldn't move/ She just was unable to get out of bed for 2 days"; BEDRIDDEN (non-serious), outcome "unknown", described as "She just was unable to get out of bed for 2 days."; DECREASED APPETITE (non-serious), outcome "unknown", described as "She wasn't eating". Additional information: The patient stated that when she was young, she was on Pfizer's birth control, and she had issues with hot flashes and had to go on hormone replacement. She had issues with hot flashes early and then when she started menopause, they took her off everything and put her on Prempro. She had issues with hot flashes as she got older and then menopause. She was put on a low dosage of birth control because of it which was hormone replacement. She was not able to sleep due to hot flashes. She has always had corporate drug coverage, and they would cover all of her medications 100%. Her husband passed away, so she had to get insurance, and got another plan too. She was fine after her first covid shot. Her second one three weeks later she got at 8 am on a Sunday. At 5 pm that same day, she couldn't move. She had to lay down. She was so nauseous. She was in bed for 3 days. She wasn't eating. She never vomited. She then took a booster dose, and experienced the same thing, but did not have nausea. She just was unable to get out of bed for 2 days. Since the second shot to now, she has had 3 instances where she felt the same way. Like that overwhelming need to lay down. Once it happened when she was outside walking. The second, she was doing laundry and instead of folding laundry right there she threw it in basket and came to her apartment. The 3rd time, she was in her apartment doing something and had to lay down. She gets checked by her doctor twice a year, and nothing was going on. She would just get that same feeling suddenly. And then she was fine. She would now be one month without Prempro because of this. No investigation reported. She still planned to get another booster in Jan2023. She had to talk to her doctor. She never got flu symptoms from the vaccines.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Blood pressure high; Difficulty sleeping (She is not able to sleep due to hot flashes); Hormone replacement therapy (She was put on a low dosage of birth control because of it which is hormone replacement.); Hot flashes (issues with hot flashes and had to go on hormone replacement); Menopause (hot flashes early, then when she started menopause, took her off everything and put her on Prempro); Thyroid disorder
Andere Medikamente
LOSARTAN; FUROSEMIDE; LEVOTHYROXINE
Allergien
-
Vorherige Impfungen
-

VAERS 2500606

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
MI
Alter
74,0
Geschlecht
F
Eingang
07.11.2022
Impfdatum
24.02.2022
Beginn
27.10.2022
Tage bis Beginn
245,0
Dosis
3
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Asthenia Bacterial test positive Biopsy artery normal Blood creatinine increased Blood test abnormal C-reactive protein increased COVID-19 Chest X-ray normal Chest discomfort Computerised tomogram normal Cough Culture urine positive Decreased appetite Differential white blood cell count normal Dizziness Dyspnoea Escherichia test positive Full blood count normal

Symptomtext

Discharge Provider: MD Primary Care Provider at Discharge: DO Admission Date: 10/27/2022 Discharge Date: 10/29/2022 HOSPITAL COURSE: Patient is a 75 y.o. female presented to the emergency department due to acute on chronic weakness. She was initially diagnosed with COVID on 10/25/2022 and was discharged home, however, she re-presented on 10/20 07/2022 with generalized weakness and feeling like she was going to faint at home. She also endorsed cough, sore throat, shortness of breath. At the time presentation to the emergency department she was afebrile with vital signs remarkable for tachypnea at 20 breaths per minute. She remained on room air.Chest x-ray imaging revealed no acute cardiopulmonary process. Lbs demonstrated creatinine of 1.26 consistent with baseline renal dysfunction. Complete blood count with diff without leukocytosis. Urinalysis is positive for nitrites, moderate leukocytes with 23.2 white blood cells and many bacteria. She is given a dose of antibiotics and admitted to floor. Urine cultures demonstrated E coli. She was subsequently treated with Rocephin x2 doses while inpatient and transitioned to oral Keflex for a total of 5 day course of antibiotics. She remained relatively asymptomatic and on room air from a COVID standpoint. She was not starting on Paxlovid due to interactions with other medications. She was not a candidate for steroids or remdesivir. PT / OT evaluated and home with home health care. She became stronger and closer to physical baseline prior to discharge. She was discharged on 10/29/2022 in stable and improved condition with the remainder of oral Keflex to complete 5 days of antibiotics for urinary tract infection. She will be receiving home health care through Home Healthcare who could provide skilled nursing as well as PT and OT services.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
10/25/2022 ED visit: 75-year-old female presenting emergency department with concerns of cough and shortness of breath. She also has pleuritic chest discomfort. On exam she is in no acute distress. Vital signs are stable. She does have faint expiratory wheezing bilaterally. Does not appear volume overloaded. COVID-19 PCR is positive. Initial troponin is indeterminate at 23. BMP within normal limits. Chest x-ray negative for acute abnormality. Complete blood count and CMP are largely unremarkable. Repeat troponin has a delta of -4. Did discuss that the patient prescription for Paxlovid. She would like to pursue this. I spoke with the pharmacy regarding medication interactions which she unfortunately does have a significant interaction with Seroquel. Does not recommended to prescribed Paxlovid with Seroquel due to the interaction in pharmacy recommended against this. I discussed this with the patient and she is understanding. I did prescribe albuterol inhaler to help with her wheezing and shortness of breath. Otherwise recommended Tylenol for pain/fever control and close follow-up with her primary care provider. She is otherwise feeling improved and is comfortable with discharge home and she is stable to do so. Given appropriate return precautions. All questions answered. Discharged home in stable condition. 9/27/2022 ED visit: The patient presents today with headache. Patient states she has been dealing with headaches over the past year. Over the past 2 days she has had increased is pain that she describes over the temporal region with photophobia and phonophobia. She did try Tylenol without relief. She states that she is currently on prednisone from her rheumatologist and with this she cannot sleep. She has also had decreased appetite and poor oral intake. Patient has benign neurologic examination that she does endorse progressively worsening headaches, is significantly hypertensive on examination is endorsing few days of vision and speech changes. With this will obtain a head CT. I did review multiple notes from rheumatology most recently on 09/03/2022 per note patient has had ultrasound of the temporal artery and biopsies which came back normal but symptoms are in line with temporal arteritis. That day they restarted prednisone taper, and ordered repeat temporal artery biopsy. She then underwent a temporal artery ultrasound which is negative for arteritis. Blood work overall looks reassuring. Sed rate and CRP are only slightly elevated and does down trending from previous. CT scan showed no acute bleed. Near complete opacification of the bilateral sphenoid sinuses with air-fluid levels. Per Radiology this could be sinusitis. Patient is not having pressure over her sinuses. She denies any recent cough or congestion. She denies any fevers. She is afebrile. I will not start antibiotics at this time. Blood pressure did improve with labetalol. Headache did improve with medication and down trending of her hypertension. Urinalysis without signs of infection. Patient on re-evaluation states she is feeling significantly better and would like to go home at this time. I do feel she is stable for discharge. She is instructed to follow up with her primary care provider as well as rheumatologist.
Vorgeschichte
Dyspnea on exertion Shortness of breath Coronary artery disease involving native coronary artery of native heart without angina pectoris Essential hypertension CHF (congestive heart failure) (HCC) GAVE (gastric antral vascular ectasia) Bilateral carotid artery stenosis Giant cell arteritis (HCC) SBO (small bowel obstruction) (HCC) GI bleed Morbid obesity with BMI of 45.0-49.9, adult (HCC) Gastrointestinal hemorrhage with melena Gastritis and duodenitis Gastroesophageal reflux disease without esophagitis Slow transit constipation Acute cystitis with hematuria UTI (urinary tract infection) Meningitis Recurrent urinary tract infection Acute cystitis without hematuria Acute on chronic anemia ESR raised Anemia Fibromyalgia Chest pain PMR (polymyalgia rheumatica) (HCC) Chronic bilateral low back pain with left-sided sciatica Neuropathy involving both lower extremities Chronic kidney disease, stage III (moderate) (HCC) Mixed hyperlipidemia Diabetes mellitus, type II (HCC) Hyperkalemia Type 2 diabetes mellitus with hyperglycemia (HCC) Hyperlipidemia RA (rheumatoid arthritis) (HCC) Depression Lower extremity edema Prsnl hx of TIA (TIA), and cereb infrc w/o resid deficits Bilateral lower extremity edema
Andere Medikamente
acetaminophen (TYLENOL) 325 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amLODIPine (NORVASC) 5 MG tablet aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 40 MG tablet buPROPion (WELLBU
Allergien
Tetracycline Metformin Sulfamethoxazole W-trimethoprim Desipramine
Vorherige Impfungen
-

VAERS 2484115

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NJ
Alter
59,0
Geschlecht
F
Eingang
20.10.2022
Impfdatum
25.02.2022
Beginn
25.02.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Feeling hot Palpitations

Symptomtext

Do noy remember if left or right arm. After sitting for a few minutes i started to feel very hot heart racing and lightheaded BP taken was 159/95 i was given water and had blood pressure checked every 15 minutes for 3 hours last BP check was 131/85. Since first vaccine i have felt my heart goes up more often not sure if related or not

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
No just followed up withy cardiologist
Aktuelle Erkrankungen
None
Vorgeschichte
Blood pressure since menopause started and on thyroid meds post r thyroidectomy in 2010 Had reaction with blood pressure shooting up since first vaccine high heart rate
Andere Medikamente
Metoprolol 25 ER mg Levothyroxine 25mcg Fish oil Blood pressure support blue bonnett Ip-6&inoitol Natures Way
Allergien
Peppers Some apples Cinnamon
Vorherige Impfungen
-

VAERS 2473416

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
MI
Alter
51,0
Geschlecht
M
Eingang
10.10.2022
Impfdatum
12.01.2022
Beginn
01.10.2022
Tage bis Beginn
262,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Computerised tomogram thorax normal Cough Dyspnoea Hypoxia Influenza like illness Respiratory failure Respiratory tract congestion SARS-CoV-2 test positive Tachycardia X-ray normal

Symptomtext

Admission Date: 10/1/2022 Discharge Date: Oct 2, 2022 PRESENTING PROBLEM: Hypoxia [R09.02] Respiratory failure with hypoxia (HCC) [J96.91] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 52-year-old male with past medical history significant for type 2 diabetes, OSA and chronic diastolic heart failure presented to the emergency department with chief complaint of dyspnea shortness of breath. Patient was having flu-like symptoms since 09/24/2022, worsening congestion shortness of breath with cough. Patient was tachycardic and hypoxic on presentation, is placing 4 L of oxygen, he tested positive for COVID-19. X-ray was negative for acute process, he had CT PE done which was negative for PE. Patient was treated with DuoNebs, albuterol and dexamethasone. Patient tolerated well, his tachycardia resolved, he was weaned off oxygen to room air with ambulation, no sputum production. He was tolerating diet and back to baseline. Patient was medically stable to be discharged on 10/02/2022 in afternoon. Was given Decadron prescription for 5 more days. He was also given prescription for albuterol as needed. Instructed patient to return to the hospital if he has worsening symptoms. Patient was vaccinated x2

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
12/13/2021- Endoscopy (Dysphagia)
Vorgeschichte
Type 2 diabetes mellitus without complication, with long-term current use of insulin (HCC) Thyroid mass Bipolar II disorder (HCC) Morbidly obese (HCC) OSA (obstructive sleep apnea) Other chest pain Chronic diastolic heart failure (HCC) Acute respiratory failure with hypoxia (HCC) Debility Dyslipidemia Essential hypertension Long-term insulin use (HCC) Insulin resistance Gastroesophageal reflux disease without esophagitis Coronary artery disease involving native coronary artery of native heart without angina pectoris Presbyopia of both eyes Respiratory failure with hypoxia (HCC)
Andere Medikamente
acetaminophen (TYLENOL) 325 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler aripiprazole (ABILIFY) 10 MG disintegrating tablet aspirin EC 81 MG enteric coated tablet atorvastatin (LIPITOR) 20
Allergien
None
Vorherige Impfungen
-

VAERS 2453582

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
MI
Alter
18,0
Geschlecht
F
Eingang
21.09.2022
Impfdatum
22.05.2021
Beginn
26.08.2022
Tage bis Beginn
461,0
Dosis
3
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja
COVID-19 Cough Dyspnoea SARS-CoV-2 test positive

Symptomtext

Pt to ED 9/4 for SOB and cough. COVID+ 8/26 at urgent care, symptoms progressively getting worse. 9/5 no anti-COVID rx needed, no signs of acute distress. Pt discharged 9/6.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
3,0
Labordaten
see above
Aktuelle Erkrankungen
None
Vorgeschichte
Asthma exacerbation, Mild persistent asthma with status asthmaticus, Asthma with exacerbation, BMI > 99% for age
Andere Medikamente
albuterol, budesonide-formoterol
Allergien
Banana
Vorherige Impfungen
-

VAERS 2427618

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
MI
Alter
12,0
Geschlecht
F
Eingang
02.09.2022
Impfdatum
01.02.2022
Beginn
26.08.2022
Tage bis Beginn
206,0
Dosis
3
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Chemotherapy Condition aggravated Cough Disease progression Dyspnoea Hepatocellular carcinoma Hypertransaminasaemia Infusion Pain Pyrexia Radiotherapy Red blood cell transfusion Respiratory viral panel SARS-CoV-2 test positive Scan abnormal Sepsis

Symptomtext

Primary Care Physician at Discharge: MD Hematologist/Oncologist: MD Admission Date: 8/26/2022 Discharge Date: 8/27/2022 PRESENTING PROBLEM: Severe sepsis Hepatocellular carcinoma, fibrolamellar HOSPITAL COURSE: The patient is a 13 y.o. female with metastatic fibrolamellar hepatocellular carcinoma diagnosed March 2019. She has had progressive disease in spite of multiple therapies with most recent therapy of IV Gemcitabine/IV Nivolumab/PO Lenvatinib/PO Quecertin + celebrex. She was admitted 8/15 with new onset dyspnea. Scans at that time noted interval progression. Patient's chemo regime was stopped and she stabilized from a clinical respiratory stand point. She began palliative radiation therapy 8/22. She was last seen in clinic 8/23 for Nivolumab and 8/24 for PRBC transfusion. Prior to presentation, patient had been clinically well and attending school. Patient came to the ED early on 8/26 with new onset fever, cough and increased WOB. She required pain control and oxygen via nasal cannula in the ED. She received a fast break with cefepime. RVP returned positive for COVID and started on Decadron as she was inelgiable for other antivirals from her transmanitis.. She was admitted to the floor for oxygen supplementation that she was able to be weaned from shortly after admission. She was continued on rocephin daily while admitted. Her home penicillin was held while she received IV abx. On admission, patient noted worsening pain that had not been covered by home regime. Pain and palliative was consulted. They were able to start a Fentanyl patch 12mcg to be changed every 72 hours with Oxycodone 15mg Q4 hours. Mom was instructed that if her pain was not controlled on this she could contact pediatric palliative care in order to increase the regimen. At time of discharge, she is to continue Decadron 6mg QD to complete on 9/2/2022 and will have palliative radiation continued with next appointment on 8/29/2022.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
1/4/2022 Oncology Infusion 1/18/2022 Oncology Infusion 2/1/2022 Oncology Infusion
Vorgeschichte
Hepatocellular carcinoma, fibrolamellar Acquired anomaly of pulmonary artery Constipation Asplenia after surgical procedure Common variable immunodeficiency with predominant immunoregulatory t-cell disorders Thrombocytosis after splenectomy Anemia due to antineoplastic chemotherapy Encounter for antineoplastic immunotherapy Acquired asplenia Central line complication, subsequent encounter Rib pain on left side Transaminitis At risk for allergic reaction to medication Hypertension Hypothyroidism Elevated blood pressure reading without diagnosis of hypertension Dyspnea Secondary malignant neoplasm of bone Secondary malignancy of anterior mediastinum Encounter for blood transfusion COVID
Andere Medikamente
acetaminophen (TYLENOL) 500 MG tablet dexamethasone (DECADRON) 6 MG tablet fentaNYL (DURAGESIC) 12 MCG/HR patch fentaNYL (DURAGESIC) 25 MCG/HR patch ibuprofen (MOTRIN) 200 MG tablet levothyroxine (SYNTHROID) 112 MCG tablet lidocaine-priloca
Allergien
SorafenibOther, Rash, Agitation Adhesive Tape Remover Pad Bactrim [Sulfamethoxazole W-trimethoprim]Itching Narcotics Other (Surgical Glue)
Vorherige Impfungen
-

VAERS 2421119

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
TX
Alter
34,0
Geschlecht
M
Eingang
26.08.2022
Impfdatum
01.03.2022
Beginn
06.05.2022
Tage bis Beginn
66,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein
Blood pressure increased Blood test normal Cardiac stress test normal Chest discomfort Chest pain Computerised tomogram normal Dyspnoea Electrocardiogram normal Headache Heart rate increased Palpitations Vision blurred

Symptomtext

On May 6th 2022, I had a sudden onset rapid heart rate and chest pressure. I could feel my pulse and blood rushing through my carotid artery. It became difficult to take a deep breath and was feeling short of breath. I checked my blood pressure and it was severely elevated at 220/130. I have no history of heart conditions nor hypertension. This episode began at 9:00 AM and I went to the ER at 5:30 PM because the symptoms had not subsided. They gave me a beta blocker to decrease my heart and blood pressure. I was discharged given a prescription for hydrachlorothiazide. I followed up with my primary care provider and has been on a care plan since than. I?ve also had multiple repeat episodes, and have been to the ER on multiple occasions for chest pain and palpitations as well as severely elevated blood pressure with symptoms of blurred vision, intense headache.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
1,0
Labordaten
ECG, CT Scans, blood work have all been negative for signs of injury or blockage to my heart. Perform a cardiac stress test which was negative and now I will be placed on a heart monitor so the doctors can see when the event actually happens.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2414987

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
WA
Alter
95,0
Geschlecht
F
Eingang
18.08.2022
Impfdatum
11.01.2022
Beginn
10.08.2022
Tage bis Beginn
211,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Asthenia COVID-19 Condition aggravated Dementia Metabolic encephalopathy SARS-CoV-2 test positive

Symptomtext

Patient received Janssen COVID vaccine on 4/6/21 (lot #202A21A) and Pfizer COVID vaccine on 1/11/22 (lot #FJ5683). On 8/10/22, patient tested positive for COVID and admitted to our inpatient facility (med/surg unit) with generalized weakness and acute metabolic encephalopathy in the setting of COVID infection and dementia. As of today (8/18/22), patient is still admitted in the med/surg unit.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
8,0
Labordaten
COVID status positive 8/10/22.
Aktuelle Erkrankungen
-
Vorgeschichte
medical history significant for mild dementia, hypertension, hyperlipidemia, paroxysmal A. fib, left bundle branch block and bradycardia, history of breast cancer status post lumpectomy, TIA, legally blind due to macular degeneration and glaucoma, and sarcoma in the left forearm status post resection
Andere Medikamente
acetaminophen, atorvastatin, calcium carbonate, donepezil, Lidoderm patch, prochlorperazine, tramadol
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2402967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
MI
Alter
49,0
Geschlecht
F
Eingang
05.08.2022
Impfdatum
24.12.2021
Beginn
26.07.2022
Tage bis Beginn
214,0
Dosis
2
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Abdominal pain lower Back pain Blood calcium normal COVID-19 Computerised tomogram abnormal Cystoscopy Drainage Dyspnoea Lithiasis Medical diet Nasal congestion Nausea Polyuria Productive cough Purulent discharge SARS-CoV-2 test positive Ureteral stent insertion Ureterolithiasis

Symptomtext

7/26--8/2 50 y/o with a h/o CHF sarcoidosis, asthma, HTN, DM came in complaining of left lower back and left lower quadrant abdominal pain, onset one day prior to arrival. With associated polyuria, NV. Additionally, complained of productive cough, nasal congestion, and SOB. CT showed multiple bilateral calculi, with the largest being a 8 mm stone in the L ureter. Patient brought to surgery by Urology and had a cystoscopy with left ureteral stent placement. Copious amounts of pus was drained after stent placement. Patient was started on IV NS, Morphone, and Azo prn. Zofran was available for nausea and we started patient of low oxalate diet. Ca was WNL, Vit D 25 was low, but Vit D 50,000 U qweek was dc'd. Pain regimen was transitioned to Toradol, Norco, and Dilaudid. Patient did not have further urinary sx. Was instructed to follow up with Urology outpatient for stent removal and was sent home on Naproxen BID and short course of Norco.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
7,0
Labordaten
7/26 -- SARS-CoV-2 by NAA, detected
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2401310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NY
Alter
73,0
Geschlecht
F
Eingang
04.08.2022
Impfdatum
27.01.2022
Beginn
08.06.2022
Tage bis Beginn
132,0
Dosis
4
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Blood test Chest X-ray Chest pain Ultrasound scan

Symptomtext

06/08/2022 I went to see my cardiologist I told him that I was having chest pain nothing was ruled out at that time. on 06/10/2022 my husband took me to the hospital at 22:00 because I was having severe chest pains. I stayed in the hospital from 06/10/2022 -06/13/2022 for 4 days . I was on so many different medications while I was in the .hospital. They did several tests including blood tests. They gave me Morphine; Pantoprazole 40miligrams; Prednisone first week 4 capsules, second week 3 capsules , third week 2 capsules and fourth week 1 capsule. I was also on heavy dose of Advil 600miligrams 4 dose per day . I will be going to the cardiologist on 08/09/2022.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
4,0
Labordaten
Chest x-ray; Blood work; ultrasounds
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Irbesartan; Hydrochlorothiazide; Atorvastatin; Aspirin; B12
Allergien
Penicillin; Naprosyn; Steroids;
Vorherige Impfungen
Tetanus shot few years ago

VAERS 2398057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
MS
Alter
48,0
Geschlecht
F
Eingang
01.08.2022
Impfdatum
28.01.2022
Beginn
07.03.2022
Tage bis Beginn
38,0
Dosis
4
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Biopsy uterus Blood test Chest pain Dyspnoea Full blood count abnormal Haemorrhage

Symptomtext

I just started bleeding after week one in March and it lasted 3 weeks. The same thing happened in April and then May I bleed the entire month all except one day. I had an appointment in May, but I couldn't go because of the cost. I went to the emergency room because I was having shortness of breath, chest pain and the bleeding made my blood count very low. The emergency doctor was saying the blood count was so low and referred me back to the OB doctor. I called my OB doctor, but he told me I needed to get surgery for birth control or ablation or a hysterectomy alt. to eliminate the amount of bleeding. I told the doctor that I really didn't want to go through surgery again since I just got a kidney transplant 3 years ago. I have started to eat foods that increase my platelets (B12 collagens, vitamin C).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Womb sample; blood test
Aktuelle Erkrankungen
N/A
Vorgeschichte
Born with small kidney (7/20/2019 Kidney surgery)
Andere Medikamente
Mycophenolate; atenolol; aspirin; prednisone; magnesium oxide; tacrolimus; ferrous sulfate; acyclovir; B12; vitamin D
Allergien
Sulfa; tramadol
Vorherige Impfungen
-

VAERS 2362566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
MN
Alter
66,0
Geschlecht
M
Eingang
08.07.2022
Impfdatum
23.01.2021
Beginn
07.06.2022
Tage bis Beginn
500,0
Dosis
4
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Chest pain Chills Dyspnoea Flank pain Pyrexia SARS-CoV-2 test positive

Symptomtext

FLANK PAIN, CHILLS, INTERMITTENT CHEST PAIN AND INCREASED WORK OF BREATHING, FEVER

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
2,0
Labordaten
POSITIVE COVID TEST 6/9/22
Aktuelle Erkrankungen
-
Vorgeschichte
Lymphoma Dyslipidemia Severe sepsis Thrombocytopenia Pancytopenia Extranodal Marginal Zone B Cell Lymphoma Of Mucosa Associated Lymphoid Tissue Lymphoma Closure Atrial Septal Defect Status Post Hypertension Essential Primary Atherosclerotic Heart Disease Of Native Coronary Artery Without Angina Pectoris Hyperlipidemia On Treatment Bundle Branch Block Bifascicular Mass Lung
Andere Medikamente
cetirizine (ZyrTEC) 10 mg tablet B complex-vitamins (BALANCE B-50) tablet clobetasoL (TEMOVATE) 0.05 % gel atorvastatin (LIPITOR) 40 mg tablet cholecalciferol (VITAMIN D3) 50 mcg (2,000 Unit) tablet diphenhydrAMINE-acetaminophen (
Allergien
Rituximab
Vorherige Impfungen
-

VAERS 2313135

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
-
Alter
51,0
Geschlecht
F
Eingang
08.06.2022
Impfdatum
08.03.2022
Beginn
08.03.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal pain Arthralgia Back pain Dizziness exertional Dysgeusia Dyspepsia Dyspnoea Ear pain External compression headache Fatigue Gait disturbance Head discomfort Headache Hypersensitivity Immunisation reaction Injected limb mobility decreased Injection site pain Injection site pruritus

Symptomtext

The Symptom's I informed her of was as followed: 1. Area of injection having a burning sensation 2. Area of injection itching 3. I couldn't lift the arm that had the injection 4. A metallic taste in my mouth 5. cramping in my abdominal area 6. Spotting/bleeding- continuous feeling of getting my mensural Cycle 7. Severe Headache/ pressure in my head- feels like I have a vice on my head when it's not pulsating with a headache 8. Pressure behind my right eye 9. Extreme Fatigue 10. soreness in my right ear 11. Dizziness when I moved around a lot which is accompanied by nausea 12. Winded 13. Veins on both hands felt sensitive and swollen 14. bad muscle aches with my lower back feeling as if my muscles were being ripped apart 15. Joint ache to where I was not able to walk on my ankles and compared it to when I was on prednisone of which she determined it could have been becoming toxic and switched my medication to Azathioprine 16. Heart burn feeling and told her the time I seen Dr. my chest area was slightly sore to touch 17. weakness in my arms and hands

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
diagnosed with Adverse effect of Covid-19 vaccine (T50.B954)
Aktuelle Erkrankungen
1. Lupus 2. High liver Enzymes which was not certain if it was due to fatty liver
Vorgeschichte
1. Lupus 2. High Liver Enzymes
Andere Medikamente
1. (Imuran) Azathioprine 50 mg 2. Vitamin C 1000 mg per/day 3. Vitamin D3 2000 iu per/day
Allergien
1. In 2018 I was taken off prednisone, for lupus, because it was believed to have been the cause for me not being able to walk on my ankles 2. When I took the Flu Vaccine it would cause me to be out for about 1-1/5 months.
Vorherige Impfungen
Flu Vaccine - last in November 2019

VAERS 2307466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CA
Alter
49,0
Geschlecht
F
Eingang
02.06.2022
Impfdatum
24.02.2022
Beginn
24.02.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Mobility decreased

Symptomtext

PATIENT SAYS THEY HAVE DIFFICULTY LIFTING RIGHT ARM. VAR FORM SAYS VACCINE GIVEN IN LEFT ARM

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2281066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
-
Alter
32,0
Geschlecht
F
Eingang
17.05.2022
Impfdatum
03.05.2022
Beginn
04.05.2022
Tage bis Beginn
1,0
Dosis
2
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chest X-ray Cough Dyspnoea Full blood count Metabolic function test

Symptomtext

New cough and dyspnea within 48 hours of receiving second Pfizer dose

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
CBC BMP chest x-ray 5/10/2022
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2277830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

moderat
Staat
MN
Alter
70,0
Geschlecht
M
Eingang
15.05.2022
Impfdatum
13.05.2022
Beginn
14.05.2022
Tage bis Beginn
1,0
Dosis
4
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Chills Dizziness Dyspnoea Fatigue Headache

Symptomtext

Headache, joint pain, chills, fatigue, dizziness, shortness of breath

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
diabetes, high blood pressure
Vorgeschichte
diabetes
Andere Medikamente
metformin, lysinopril, glipiside
Allergien
none known
Vorherige Impfungen
same symptoms after first booster

VAERS 2267867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
VA
Alter
69,0
Geschlecht
F
Eingang
09.05.2022
Impfdatum
15.04.2022
Beginn
02.05.2022
Tage bis Beginn
17,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Atrial fibrillation COVID-19 Condition aggravated Cough Fatigue Feeling abnormal Headache Heart rate decreased Myalgia Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test Vaccine breakthrough infection

Symptomtext

I had a breakthrough infection beginning May 2, 2022. My symptoms began with headache, sore throat, congestion, fatigue, muscle aches and cough came later on. I did have an exceptionally low heart rate, low 40 for about 6 hours. In the middle of this I also had AFIB. This was day 4 after diagnosed. It is now day 8 and I still have fatigue, brain fog, and headache.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
Home nasal swab, three times
Aktuelle Erkrankungen
Respiratory virus on March 27, 2022.
Vorgeschichte
COPD Hypertension High cholesterol Heart arrhythmia/ A fib
Andere Medikamente
Omeprazole Simvastatin Benazepril Montelukast Amlodipine Elliptica Incruise Calcium Vitamin D3
Allergien
Fish Zithromax Doxycycline Levofloxacin Oxytocin Vicodin Percodan Trazodone
Vorherige Impfungen
-

VAERS 2243027

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
-
Alter
34,0
Geschlecht
F
Eingang
20.04.2022
Impfdatum
12.03.2022
Beginn
01.03.2022
Tage bis Beginn
-
Dosis
3
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blindness Dysmenorrhoea Headache Lymphadenopathy Muscular weakness Ophthalmic migraine Pain Palpitations

Symptomtext

huge swollen gland under her armpit; optical migraine; her heart was jumping out of her chest/ heart palpitations; pain; she loses her vision completely in one eye; It was hard for the caller to close her arm; Headache; cramps were bad or if its real; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP), Program ID:. The reporter is the patient. A 34-year-old female patient received BNT162b2 (BNT162B2), on 12Mar2022 as dose 3 (booster), single (Lot number: FJ5683) at the age of 34 years, in left arm for covid-19 immunisation. The patient's family history included: "optical migraines" (unspecified if ongoing), notes: The caller's mother would get optical migraines when she was young. There were no concomitant medications. Vaccination history included: Bnt162b2 (Dose 1, Single, left arm), for COVID-19 immunization, reaction(s): "caller had some headaches"; Bnt162b2 (Dose 2, Single, left arm), for COVID-19 immunization, reaction(s): "caller had some headaches". The following information was reported: PALPITATIONS (non-serious) with onset 12Mar2022, outcome "unknown", described as "her heart was jumping out of her chest/ heart palpitations"; LYMPHADENOPATHY (non-serious) with onset 12Mar2022, outcome "recovered" (15Mar2022), described as "huge swollen gland under her armpit"; OPHTHALMIC MIGRAINE (non-serious) with onset 12Mar2022, outcome "unknown", described as "optical migraine"; PAIN (non-serious) with onset 12Mar2022, outcome "unknown"; HEADACHE (non-serious) with onset Mar2022, outcome "unknown"; MUSCULAR WEAKNESS (non-serious) with onset Mar2022, outcome "unknown", described as "It was hard for the caller to close her arm"; BLINDNESS (medically significant) with onset Mar2022, outcome "unknown", described as "she loses her vision completely in one eye"; DYSMENORRHOEA (non-serious) with onset 2022, outcome "unknown", described as "cramps were bad or if its real". Therapeutic measures were taken as a result of ophthalmic migraine. On 12Mar2022 the caller got an optical migraine and took a Tylenol and then she had another one on 17Mar2022 and Monday 21Mar2022. Additional information: No other conditions and investigations. After the (as reported "second") booster shot, the caller got this horrible lump under her armpit. She got a huge swollen gland under her armpit that lasted for three days. The caller noticed the lump in the evening, the lump was on the left arm and then she noticed the pain when she was moving stuff around and then she was panicked and her heart was jumping out of her chest. The heart palpitations started on the night of 12Mar2022 and continued as the same amount of time of the booster. The caller also had a normal headache and later she was getting an optical migraines where she lost her vision completely in one eye. The optical migraine its like zig zag and then the caller could not see. It was not painful but its all in the eye and then the headache follows. The caller clarified and confirmed that she got the first two shots and one booster of the Pfizer covid vaccine. The caller had to get it for her job and it made her upset because she didn't want to get the booster. The caller wanted to get it documented so people aren't forced to get another booster. The caller was going to see the doctor on Monday and see if it was correlated. It was hard for the caller to close her arm and she took Tylenol and the medic at her work said that he didn't know what to tell her because he was not getting the booster dose. The caller talked to some friends who have had strange periods and could not tell if her cramps were bad or if its real, its hard to say. The caller's mother would get optical migraines when she was younger. The caller thought this was directly correlated wit the vaccine because she knew her body. With the first two doses the caller had some headaches and the normal things she was told she would have. After the booster the caller still felt like she was recovering. She had to drink so much more water and really monitor so that she tried not to get headache. The caller hoped that she could go a month without a migraine. No Follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Ophthalmic migraine
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Ophthalmic migraine (The caller's mother would get optical migraines when she was young)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2209551

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
VA
Alter
57,0
Geschlecht
F
Eingang
12.04.2022
Impfdatum
31.03.2022
Beginn
31.03.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood pressure increased Dizziness Extra dose administered Fear Flushing Palpitations Swollen tongue

Symptomtext

I had my fourth shot on 3/31/22 at 3:27 pm. I waited 15 minutes, felt great, and left the vaccine clinic and got into my car. I drove 2 miles and at 3:50 pm my heart started pounding hard, I felt light headed, my face was flush and my tongue started to swell slightly. I became scared and called emergency. I pulled over into a parking lot. I also called my primary care doctor, but couldn't get through. I was really scared because my heart felt like it was going to explode--it was pounding so hard. I was also afraid I was in the beginning stages of an anaphylactic reaction. After about five minutes and as I was talking to the emergency operator, my heart started to calm down and I felt less faint. My tongue was still swollen, though. I decided to not waste an ambulance, but decided I needed to be with someone. I drove back to the vaccine clinic because there were nurses there. Probably not the smartest idea. They took my blood pressure, which was up to 165. They monitored me for about an hour as my symptoms subsided. I left for home with my tongue still slightly swollen. Within an hour of arriving home, my tongue felt back to normal. It was a terrifying event. However, after that I went to bed as normal and had no other side effects. Did I have a myocarditis event?

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Hashimoto hypothyroidism, Raynaud's Syndrome, high cholesterol, high blood pressure, psoriasis on head and arms, unknown household allergy
Andere Medikamente
levothyroxine 100 mcg, olmesartan 5 mg, diclofenac sod ec 75 mcg, multivitamin tablet, red yeast rice capsule, COQ-10 capsule, tumeric vitamin, claritan 10 mg tablet, apple cider vinegar gummy (2), vitamin C gummy (3)
Allergien
Codeine, IVP dye, pertussis vaccination, black mold
Vorherige Impfungen
Pertussis vaccine

VAERS 2196292

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
IL
Alter
45,0
Geschlecht
F
Eingang
24.03.2022
Impfdatum
24.03.2022
Beginn
24.03.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Adverse reaction Anxiety Chest pain Dyspnoea Headache

Symptomtext

Patient had an adverse reaction. Pt was waiting allotted time and developed severe chest pain, SOB, and headache. Pt rated pain as 8 on 0-10 pain scale in chest. Pt very anxious as to be expected. Patient was placed in reclining chair to lay back and O2 3L applied. Pt was given an 81mg Aspirin. Only systolic BP was able to be collected by M.D. and it was 160. With O2 oxygen was at 100% and pulse came down to 110 from 190s. EMS was contacted and arrived within approximately 5 min. Pt did advise she did not have any adverse reaction to her first Pfizer dose.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Unknown at this time. Patient was sent to ER via EMS.
Aktuelle Erkrankungen
n/a
Vorgeschichte
GERD, Anxiety with depression, hyperlipidemia, Reflux esophagitis, fibromyalgia, iron deficiency anemia, keratitis, insomnia, fibroadenoma of left breast, nodule of right lung, hypokalemia, morbid obesity, OSA, hyperaldosteronism, HTN, DM Type 2
Andere Medikamente
albuterol 108 (90 Base) MCG/ACT Aerosol Solution ALPRAZolam (XANAX) 0.5 MG Tablet amLODIPine (NORVASC) 10 MG Tablet atorvastatin (LIPITOR) 40 MG Tablet citalopram (CeleXA) 20 MG Tablet fluticasone (FLONASE) 50 MCG/ACT Suspension Glucose Blo
Allergien
Levofloxacin, Tramadol, Penicillin, Ranitidine
Vorherige Impfungen
-

VAERS 2195010

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NH
Alter
58,0
Geschlecht
F
Eingang
23.03.2022
Impfdatum
06.03.2022
Beginn
07.03.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein
Blood pressure diastolic increased Cardiac monitoring Feeling cold Head discomfort Hyperhidrosis Magnetic resonance imaging head Migraine Ocular discomfort Pain Palpitations Ventricular septal defect Visual impairment

Symptomtext

The morning after and for 2 days following the vaccines, patient experienced heavy sweating/soaking, feeling freezing, and body aches (without any fever). On the third day, she started feeling better, but then all of a sudden her heart started pounding, her vision starting graying and going up and down, and she had eye and head pressure. She then went to Hospital which sent her to another hospital since they supposedly did not have the expertise to help her. She was hospitalized at for 2 days and was hydrated with IV fluids, given toradol, and some other medication the patient cannot remember for her head. At CMC, doctors told her she had extremely high diastolic blood pressure and found a hole in her heart. They also did an MRI on her head. They don't know exactly what is going on, but diagnosed her with non-specific migraine in the mean time. She is still experiencing persistent migraines (7/10 pain scale) and is waiting to see a neurologist. She is also currently wearing a heart monitor and is most likely going to have to get heart surgery to repair her heart.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Migraine
Hospital-Tage
2,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
hypertension only has 1 kidney
Andere Medikamente
metoprolol atorvastatin
Allergien
nkda
Vorherige Impfungen
-

VAERS 2194893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CA
Alter
53,0
Geschlecht
M
Eingang
23.03.2022
Impfdatum
06.04.2021
Beginn
21.03.2022
Tage bis Beginn
349,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Anaemia Blood iron increased Condition aggravated Hypothyroidism Mean cell volume increased Red blood cell count decreased

Symptomtext

Comprehensive metabolic panel performed with low RBC, high mean RBC and high Iron levels. Indications of anemia and increased symptoms of Hypothyroidism despite treatment with levothyroxine 150mcg 6 days/week

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
RBC Count 3.91 million/uL Mean RBC volume 105.9 fL Mean RBC Iron 35.5pg Tested 3/18/22
Aktuelle Erkrankungen
None
Vorgeschichte
Hypothyroidism
Andere Medikamente
Tirosint, Xtend Life CX-80, Xtend Life Omega 3, Ikaria Beauty Collagen
Allergien
None
Vorherige Impfungen
-

VAERS 2182553

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
OH
Alter
26,0
Geschlecht
M
Eingang
16.03.2022
Impfdatum
15.03.2022
Beginn
15.03.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Blood test Computerised tomogram head Confusional state Electrocardiogram Headache Tremor

Symptomtext

Approx 30 minutes after vaccination, pt reports confusion, headache, tremors.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tremor
Hospital-Tage
-
Labordaten
CT head, blood work, ECG
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2182496

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
OH
Alter
66,0
Geschlecht
M
Eingang
16.03.2022
Impfdatum
15.03.2022
Beginn
15.03.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Blood test Chest pain Dizziness Electrocardiogram Hypoaesthesia Hypoaesthesia oral Pain in extremity Pruritus

Symptomtext

Approx 15 min after vaccination, pt developed chest pain, left arm pain/numbness, tongue numbness, feeling faint, itching all over.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
blood work, EKG
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
ibuprofen, insect stings
Vorherige Impfungen
-

VAERS 2182373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

moderat
Staat
PA
Alter
18,0
Geschlecht
F
Eingang
16.03.2022
Impfdatum
15.02.2022
Beginn
17.02.2022
Tage bis Beginn
2,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Dyspnoea Pyrexia

Symptomtext

Claimant alleges she was issued a Pfizer COVID-19 vaccine. The next day, she had a fever, trouble breathing, and had to be taken to the ER.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
na
Vorgeschichte
na
Andere Medikamente
na
Allergien
na
Vorherige Impfungen
-

VAERS 2181905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
-
Alter
62,0
Geschlecht
F
Eingang
16.03.2022
Impfdatum
13.01.2022
Beginn
13.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Arthritis Hypoaesthesia Pain in extremity Paraesthesia

Symptomtext

tingling; numbness; pain in the feet/pain in her feet and ankles; pain in her feet and ankles; arthritis; This is a spontaneous report received from a contactable reporter(s) (Pharmacist) from medical information team. A 62 year-old female patient received bnt162b2 (BNT162B2), administration date 13Jan2022 11:30 (Lot number: FJ5683) at the age of 62 years as dose 1, single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: PARAESTHESIA (non-serious) with onset 13Jan2022, outcome "unknown", described as "tingling"; HYPOAESTHESIA (non-serious) with onset 13Jan2022, outcome "unknown", described as "numbness"; PAIN IN EXTREMITY (non-serious) with onset 13Jan2022, outcome "unknown", described as "pain in the feet/pain in her feet and ankles"; ARTHRALGIA (non-serious) with onset 13Jan2022, outcome "unknown", described as "pain in her feet and ankles"; ARTHRITIS (non-serious) with onset 13Jan2022, outcome "unknown", described as "arthritis". Additional Context: Caller was a pharmacist at # that was calling about a patient who received her 1st adult gray cap Pfizer BioNTech Covid-19 vaccine this morning at around 11:30 AM. Caller stated the patient called her later today and states she was experiencing tingling, numbness and pain in the feet. Caller stated the patient was treated for arthritis already and this seems coincidental. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2162013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj5683

moderat
Staat
NY
Alter
41,0
Geschlecht
F
Eingang
16.03.2022
Impfdatum
21.02.2022
Beginn
21.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arrhythmia Hypoaesthesia Hypoaesthesia oral

Symptomtext

Arrhythmia; I have numbness in my right arm and fingertips; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 41 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 21Feb2022 16:30 (Lot number: Fj5683) at the age of 41 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Arrhythmia- still performing test" (unspecified if ongoing); "Penicillin allergy" (unspecified if ongoing); "covid" (unspecified if ongoing). No other vaccine in four weeks. Prior to vaccination, the patient was diagnosed with covid-19. Post vaccination, the patient had not been tested for covid-19. Concomitant medication(s) received within two weeks included: NAPROXEN [NAPROXEN SODIUM]; CYCLOBENZAPRINE. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: El8982, Location of injection: Arm Right, Vaccine Administration Time: 12:00 PM), administration date: 09Feb2021, when the patient was 40 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: El3249, Location of injection: Arm Right, Vaccine Administration Time: 03:00 PM), administration date: 19Jan2021, when the patient was 40 years old, for Covid-19 immunization. The following information was reported: ARRHYTHMIA (medically significant) with onset 21Feb2022 16:45, outcome "not recovered", described as "Arrhythmia"; HYPOAESTHESIA (non-serious) with onset 21Feb2022 16:45, outcome "not recovered", described as "I have numbness in my right arm and fingertips". The events "arrhythmia" and "i have numbness in my right arm and fingertips" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of arrhythmia, hypoaesthesia.; Sender's Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal association between the events and suspect drug BNT162B2 cannot be 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
Arrhythmia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Arrhythmia; COVID-19; Penicillin allergy
Andere Medikamente
NAPROXEN [NAPROXEN SODIUM]; CYCLOBENZAPRINE
Allergien
-
Vorherige Impfungen
-

VAERS 2162013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj5683

moderat
Staat
NY
Alter
41,0
Geschlecht
F
Eingang
16.03.2022
Impfdatum
21.02.2022
Beginn
21.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arrhythmia Hypoaesthesia Hypoaesthesia oral

Symptomtext

Arrhythmia; I have numbness in my right arm and fingertips; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 41 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 21Feb2022 16:30 (Lot number: Fj5683) at the age of 41 years as dose 3 (booster), single for covid-19 immunisation. Relevant medical history included: "Arrhythmia- still performing test" (unspecified if ongoing); "Penicillin allergy" (unspecified if ongoing); "covid" (unspecified if ongoing). No other vaccine in four weeks. Prior to vaccination, the patient was diagnosed with covid-19. Post vaccination, the patient had not been tested for covid-19. Concomitant medication(s) received within two weeks included: NAPROXEN [NAPROXEN SODIUM]; CYCLOBENZAPRINE. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: El8982, Location of injection: Arm Right, Vaccine Administration Time: 12:00 PM), administration date: 09Feb2021, when the patient was 40 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: El3249, Location of injection: Arm Right, Vaccine Administration Time: 03:00 PM), administration date: 19Jan2021, when the patient was 40 years old, for Covid-19 immunization. The following information was reported: ARRHYTHMIA (medically significant) with onset 21Feb2022 16:45, outcome "not recovered", described as "Arrhythmia"; HYPOAESTHESIA (non-serious) with onset 21Feb2022 16:45, outcome "not recovered", described as "I have numbness in my right arm and fingertips". The events "arrhythmia" and "i have numbness in my right arm and fingertips" were evaluated at the physician office visit. Therapeutic measures were not taken as a result of arrhythmia, hypoaesthesia.; Sender's Comments: Based on the information in the case report and a plausible temporal relationship, a possible causal association between the events and suspect drug BNT162B2 cannot be 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
Arrhythmia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Arrhythmia; COVID-19; Penicillin allergy
Andere Medikamente
NAPROXEN [NAPROXEN SODIUM]; CYCLOBENZAPRINE
Allergien
-
Vorherige Impfungen
-

VAERS 2168165

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
GA
Alter
19,0
Geschlecht
F
Eingang
09.03.2022
Impfdatum
07.02.2022
Beginn
15.02.2022
Tage bis Beginn
8,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood pressure increased Chest X-ray abnormal Chest pain Computerised tomogram thorax normal Dyspnoea Electrocardiogram Fibrin D dimer increased Inflammation Palpitations

Symptomtext

I got the shot on February 7, 2022 at around 6 PM. On February 15, 2022 around 12 AM I woke up with awful chest pains, I tried multiple things to try and ease it off. I drank hot tea, soda to see if it was maybe a gas pain, took some tums, and when I got to clinical I talked to my instructor. She gave me a gas x and took me to get my Vital Signs. My blood pressure was 150/95 and my blood pressure is never that high, i'm a really healthy individual my blood pressure stays around 118/74. Later that night i started to have heart palpitations where it felt like my heart was beating out of my chest, excruciating chest pains, and shortness of breath. I went to the ER the next day and they were giving me medication to help with chest pain. They did an EKG, chest X-ray, and CT scan of my chest. I started to see a cardiologist about my chest pain and he has been running test and prescribed me medication. I told him i started to experience chest pains, heart palpitations, and shortness of breathe after the 1st dose of covid vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Chest X-ray they said i had some inflammation in my chest, they did a CT to check for a clot because my D-dimer was elevated and they said there were no signs of clots. They didn't tell me anything about my EKG.
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
Birth control
Allergien
codine
Vorherige Impfungen
-

VAERS 2158158

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NY
Alter
42,0
Geschlecht
F
Eingang
04.03.2022
Impfdatum
04.03.2022
Beginn
04.03.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Dyspnoea Heart rate increased Tachycardia

Symptomtext

Patient completed first dose of Pfizer Vaccine and sat in observation for 20 minutes and then started to complain about difficulty breathing and fast heart rate. Three sets of vital signs initiated with abnormal results showing tachycardic. EMS activated at 0415 pm and arrived at 04:26 pm. patient was transferred to hospital at 04:46pm. hotline called, DOH notified.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
none
Vorgeschichte
unknown
Andere Medikamente
N/A
Allergien
tetracyclines
Vorherige Impfungen
-

VAERS 2154602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
MA
Alter
41,0
Geschlecht
F
Eingang
03.03.2022
Impfdatum
01.03.2022
Beginn
02.03.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chest pain Lymphadenopathy Rash

Symptomtext

rash on chest and back less than 48 hours after vaccine, same with the second dose prior, rash is worse, chest pain, swollen lymph node on left armpit

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
birth control
Allergien
mango, erythromycin
Vorherige Impfungen
Pfizer 2nd dose rash

VAERS 2151289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CA
Alter
54,0
Geschlecht
F
Eingang
01.03.2022
Impfdatum
01.03.2022
Beginn
01.03.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chest pain Hypotonia Tremor Unresponsive to stimuli

Symptomtext

Patient received her COVID vaccine booster of Pfizer at 12:12. At 12:25, during the observation, patient began shaking and became unresponsive. She was slouched down in her chair, then lowered to the ground by staff, while staff held her head for safety. The shaking lasted approximately 2 minutes and patient began to become responsive about 3 minutes after the shaking began. VS: 207/115 HR 122 99% on RA. Patient reported chest pain 5/10 after the vaccine. Patient and her friend reported that she had serum syndrome with joint swelling and N/V after previous doses. Patient was very anxious and upset about getting the vaccine but told the LVN injector that the doctor would not give her a medical clearance for the booster. VS at 12:36 222/128 HR 124 98% on RA. Report given to paramedic for transport to the emergency department.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
HTN, DM 2, Obesity, White Coat Syndrome
Andere Medikamente
-
Allergien
Iron Erythromycin Penicillins Tetracycline
Vorherige Impfungen
-

VAERS 2105144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
OH
Alter
73,0
Geschlecht
F
Eingang
27.02.2022
Impfdatum
24.01.2022
Beginn
25.01.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Asthenia Balance disorder Chest pain Dysarthria Dyspnoea exertional Blood test normal COVID-19 Chest X-ray normal Dyspnoea Cardiac stress test Exercise test Fatigue Electrocardiogram normal Full blood count Heart rate irregular SARS-CoV-2 test positive Troponin normal Gait disturbance

Symptomtext

dyspnea on exertion; heart palpitations; chest pain; could not exercise with her trainer/ poor mobility, balance was bad; could not exercise with her trainer/ poor mobility, balance was bad; feeling weak and tired; feeling weak and tired; could barely walk without sitting down; kept getting these rapid heart beats; she has been slurring her words; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 24Jan2022 10:00 (Lot number: FJ5683, Expiration Date: 30Apr2022) at the age of 73 years as dose 1, 0.3 ml single for covid-19 immunisation. Relevant medical history included: "Hypertension", start date: 2008 (ongoing), notes: diagnosed she thinks in 2008.; "Covid", start date: 03Jan2022 (unspecified if ongoing), notes: she also wants to say that she tested positive for Covid on 03Jan 2022. Concomitant medication(s) included: OLMESARTAN taken for hypertension (ongoing); VIT D3; INFLUENZA VACCINE, administration date 10Jan2022; B COMPLEX WITH C. The following information was reported: DYSPNOEA EXERTIONAL (hospitalization) with onset 25Jan2022, outcome "not recovered", described as "dyspnea on exertion"; PALPITATIONS (hospitalization) with onset 25Jan2022, outcome "not recovered", described as "heart palpitations"; CHEST PAIN (hospitalization) with onset 25Jan2022, outcome "not recovered", described as "chest pain"; MOBILITY DECREASED (non-serious), BALANCE DISORDER (non-serious) all with onset 25Jan2022, outcome "not recovered" and all described as "could not exercise with her trainer/ poor mobility, balance was bad"; ASTHENIA (non-serious), FATIGUE (non-serious) all with onset 25Jan2022, outcome "unknown" and all described as "feeling weak and tired"; GAIT DISTURBANCE (non-serious) with onset 25Jan2022, outcome "unknown", described as "could barely walk without sitting down"; HEART RATE INCREASED (non-serious) with onset 2022, outcome "unknown", described as "kept getting these rapid heart beats"; DYSARTHRIA (non-serious) with onset 2022, outcome "unknown", described as "she has been slurring her words". The patient was hospitalized for dyspnoea exertional, palpitations, chest pain (start date: 01Feb2022, discharge date: 02Feb2022, hospitalization duration: 1 day(s)). The events "dyspnea on exertion", "heart palpitations", "chest pain", "could not exercise with her trainer/ poor mobility, balance was bad", "could not exercise with her trainer/ poor mobility, balance was bad", "feeling weak and tired", "feeling weak and tired", "could barely walk without sitting down", "kept getting these rapid heart beats" and "she has been slurring her words" were evaluated at the physician office visit and emergency room visit. It was reported that the day after the patient got the vaccine she started having side effects, ultimately was hospitalized overnight and was advised not to get the second dose. On 25Jan2022 when she woke up the day after the vaccine, she was experiencing dyspnea on exertion, heart palpitations and chest pain. This all started in the morning between 8 and 8:15, she had been feeling weak and tired when she woke up on the 25th, as the morning progressed, it got worse. It was stated that she was a very active person, could barely walk without sitting down, caller states she was admitted into the hospital on 01Feb2022 and discharged on 02Feb2022. When this started on the 25Jan2022, she was told not to exert herself, to rest and get plenty of fluids. All of a sudden she could not exercise with her trainer, told her she needed to be cleared with doctor to work with him again, poor mobility, balance was bad. She needed to contact her cardiologist because she kept getting rapid heartbeats. States the only thing she had was hyperstension at the time of the report, and she stated she has had for years and years and was under control. She also takes Vitamins D3 and B complex with C. For treatment she took help of physical therapist, speech therapy because she had been slurring her words, she was maintaining a heart healthy diet, stated she was vegan, stated they were putting her into the long Covid clinic, starting that to monitor her heart. She also wanted to say that she tested positive for Covid on 03Jan2022, because she was wanting her to do a stress test, they told her she needed a test first, later that night they sent her a message that she had tested positive. called CDC and told her to quarantine for 11 days so she did. Stated on 16Jan2022 she saw PCP and then on 24Jan2022 she got the COVID vaccine. There were no previous immunization with the Pfizer vaccine considered as suspect. On 10Jan2022 patient had a flu shot. No relevant tests were done.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
1,0
Labordaten
-
Aktuelle Erkrankungen
Hypertension (diagnosed she thinks in 2008.)
Vorgeschichte
Medical History/Concurrent Conditions: COVID-19 (she also wants to say that she tested positive for Covid on 03Jan 2022)
Andere Medikamente
OLMESARTAN; VIT D3; B COMPLEX WITH C
Allergien
-
Vorherige Impfungen
-

VAERS 2105144

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
OH
Alter
73,0
Geschlecht
F
Eingang
27.02.2022
Impfdatum
24.01.2022
Beginn
25.01.2022
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Asthenia Balance disorder Chest pain Dysarthria Dyspnoea exertional Blood test normal COVID-19 Chest X-ray normal Dyspnoea Cardiac stress test Exercise test Fatigue Electrocardiogram normal Full blood count Heart rate irregular SARS-CoV-2 test positive Troponin normal Gait disturbance

Symptomtext

dyspnea on exertion; heart palpitations; chest pain; could not exercise with her trainer/ poor mobility, balance was bad; could not exercise with her trainer/ poor mobility, balance was bad; feeling weak and tired; feeling weak and tired; could barely walk without sitting down; kept getting these rapid heart beats; she has been slurring her words; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 73 year-old female patient received bnt162b2 (BNT162B2), administered in arm right, administration date 24Jan2022 10:00 (Lot number: FJ5683, Expiration Date: 30Apr2022) at the age of 73 years as dose 1, 0.3 ml single for covid-19 immunisation. Relevant medical history included: "Hypertension", start date: 2008 (ongoing), notes: diagnosed she thinks in 2008.; "Covid", start date: 03Jan2022 (unspecified if ongoing), notes: she also wants to say that she tested positive for Covid on 03Jan 2022. Concomitant medication(s) included: OLMESARTAN taken for hypertension (ongoing); VIT D3; INFLUENZA VACCINE, administration date 10Jan2022; B COMPLEX WITH C. The following information was reported: DYSPNOEA EXERTIONAL (hospitalization) with onset 25Jan2022, outcome "not recovered", described as "dyspnea on exertion"; PALPITATIONS (hospitalization) with onset 25Jan2022, outcome "not recovered", described as "heart palpitations"; CHEST PAIN (hospitalization) with onset 25Jan2022, outcome "not recovered", described as "chest pain"; MOBILITY DECREASED (non-serious), BALANCE DISORDER (non-serious) all with onset 25Jan2022, outcome "not recovered" and all described as "could not exercise with her trainer/ poor mobility, balance was bad"; ASTHENIA (non-serious), FATIGUE (non-serious) all with onset 25Jan2022, outcome "unknown" and all described as "feeling weak and tired"; GAIT DISTURBANCE (non-serious) with onset 25Jan2022, outcome "unknown", described as "could barely walk without sitting down"; HEART RATE INCREASED (non-serious) with onset 2022, outcome "unknown", described as "kept getting these rapid heart beats"; DYSARTHRIA (non-serious) with onset 2022, outcome "unknown", described as "she has been slurring her words". The patient was hospitalized for dyspnoea exertional, palpitations, chest pain (start date: 01Feb2022, discharge date: 02Feb2022, hospitalization duration: 1 day(s)). The events "dyspnea on exertion", "heart palpitations", "chest pain", "could not exercise with her trainer/ poor mobility, balance was bad", "could not exercise with her trainer/ poor mobility, balance was bad", "feeling weak and tired", "feeling weak and tired", "could barely walk without sitting down", "kept getting these rapid heart beats" and "she has been slurring her words" were evaluated at the physician office visit and emergency room visit. It was reported that the day after the patient got the vaccine she started having side effects, ultimately was hospitalized overnight and was advised not to get the second dose. On 25Jan2022 when she woke up the day after the vaccine, she was experiencing dyspnea on exertion, heart palpitations and chest pain. This all started in the morning between 8 and 8:15, she had been feeling weak and tired when she woke up on the 25th, as the morning progressed, it got worse. It was stated that she was a very active person, could barely walk without sitting down, caller states she was admitted into the hospital on 01Feb2022 and discharged on 02Feb2022. When this started on the 25Jan2022, she was told not to exert herself, to rest and get plenty of fluids. All of a sudden she could not exercise with her trainer, told her she needed to be cleared with doctor to work with him again, poor mobility, balance was bad. She needed to contact her cardiologist because she kept getting rapid heartbeats. States the only thing she had was hyperstension at the time of the report, and she stated she has had for years and years and was under control. She also takes Vitamins D3 and B complex with C. For treatment she took help of physical therapist, speech therapy because she had been slurring her words, she was maintaining a heart healthy diet, stated she was vegan, stated they were putting her into the long Covid clinic, starting that to monitor her heart. She also wanted to say that she tested positive for Covid on 03Jan2022, because she was wanting her to do a stress test, they told her she needed a test first, later that night they sent her a message that she had tested positive. called CDC and told her to quarantine for 11 days so she did. Stated on 16Jan2022 she saw PCP and then on 24Jan2022 she got the COVID vaccine. There were no previous immunization with the Pfizer vaccine considered as suspect. On 10Jan2022 patient had a flu shot. No relevant tests were done.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
1,0
Labordaten
-
Aktuelle Erkrankungen
Hypertension (diagnosed she thinks in 2008.)
Vorgeschichte
Medical History/Concurrent Conditions: COVID-19 (she also wants to say that she tested positive for Covid on 03Jan 2022)
Andere Medikamente
OLMESARTAN; VIT D3; B COMPLEX WITH C
Allergien
-
Vorherige Impfungen
-

VAERS 2138178

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
WA
Alter
63,0
Geschlecht
M
Eingang
24.02.2022
Impfdatum
04.02.2022
Beginn
10.02.2022
Tage bis Beginn
6,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein
Chills Condition aggravated Limb discomfort Pyrexia Tinnitus

Symptomtext

There was no immediate reaction but a day later the left arm felt like a pulled muscle. Chills and fevers followed. These lessened somewhat but about 6 days later ringing in the ears was moderate and as of this report has not subsided. I have yet to schedule an office visit.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
occasional tinnitus - eg after long freeway drive, recovers in a few hours
Vorgeschichte
chronic fatigue illness coronary heart disease
Andere Medikamente
Metoprolol 50mg Isosorbide 60mg Atorvastatin 80mg Aspirin 81mg
Allergien
none
Vorherige Impfungen
-

VAERS 2138002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CA
Alter
43,0
Geschlecht
F
Eingang
24.02.2022
Impfdatum
13.02.2022
Beginn
14.02.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal pain lower Blood test Chest discomfort Chest pain Diarrhoea Dyspnoea Feeling cold Insomnia Muscle fatigue Neuralgia Pain in extremity Peripheral swelling

Symptomtext

Started to feel pumping heart 12 hours after injection. 24 hours later, felt the arm pain, feel cold, tight chest, short breath, 48 hours later, starting having diarrheas, lower abdominal pain, sharp nerve pain on the leg here and there, one morning experienced super fatigue left leg. 3 hours later, the feeling was gone. After 48 hours, start feel sharp pain from chest, one and off. cannot sleep. slightly swelling legs and fatigue for the legs

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Blood test, heart ultrasound (scheduled), cardio test (scheduled)
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2134621

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NY
Alter
40,0
Geschlecht
F
Eingang
23.02.2022
Impfdatum
26.01.2022
Beginn
26.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Cardiac flutter Cough Dizziness Palpitations

Symptomtext

side effects were Fluttering, heart palpitations, (a hyperbolic feeling) dizziness, coughing.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
symptoms subsided and I was able to get the second dose.
Aktuelle Erkrankungen
Quarantined due to exposure right before vaccination date
Vorgeschichte
Hashimoto's Thyroiditis
Andere Medikamente
Levothyroxine 0.100MCG
Allergien
not that I know of
Vorherige Impfungen
1/26/2022

VAERS 2129461

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
MI
Alter
50,0
Geschlecht
F
Eingang
21.02.2022
Impfdatum
15.02.2022
Beginn
15.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dyspnoea Heart rate increased Hypoaesthesia Paraesthesia

Symptomtext

Within 4 hours: Difficulty breathing; A fast heartbeat; and Numbness and tingling.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
Epilepsy/seizures, HX ovarian cancer, muscle spasms of lower extremity
Andere Medikamente
Flexeril, Keppra, Robaxin
Allergien
No Known Allergies
Vorherige Impfungen
-

VAERS 2123916

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj5683

moderat
Staat
IL
Alter
48,0
Geschlecht
F
Eingang
18.02.2022
Impfdatum
18.02.2022
Beginn
18.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Palpitations

Symptomtext

A 48year-old female walked back into the clinic 1hr 10 mins at 12:32pm after being vaccinated (Pfizer booster). Patient complained of lightheadedness, dizziness, and heart-racing. She admitted she hasn't had anything to eat nor drink for the day and has been working all morning with this being her first experience of such symptoms post-vaccination. Past Med Hx- Hypothyroidism Past Surg Hx- Nil Meds- Levothyroxine( took this morning at 4:35 am). Allergy- Nil Precautions taken : - -the patient was instructed to lay on the yoga mat while her Bp, pulse, and HR were taken. -the patient was also given water, apple juice, and some snacks. -Blood pressure, pulse, and heart rate respectively are as follows: *12:15pm was 140/92,116, 97%. *12:20pm was 128/84,102,98%. *12:28pm was 122/82, 96, 99%. No rigors or chills or dyspnea were noted. -She admitted to feeling a bit better 10 mins later and insisted on going home. Patient was advised to stay hydrated, get rest and visit the emergency department if she feels worse. P.S- I got her contact for subsequent checking in.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Hypothyroidism
Vorgeschichte
-
Andere Medikamente
Levothyroxine
Allergien
Nil
Vorherige Impfungen
-

VAERS 2113017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
FL
Alter
14,0
Geschlecht
F
Eingang
15.02.2022
Impfdatum
15.02.2022
Beginn
15.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood glucose normal Electrocardiogram normal Headache Nausea Tremor

Symptomtext

Client is a 14 year old female who received her 1st dose of the COVID-19 vaccine Pfizer to left deltoid at 10:33 am. Client observed in observation area complaining of nausea, headache, tremors. Client denies any pain or discomfort to vaccination site. Client encouraged to rest and relax. Fire Rescue arrived to scene for further evaluation. Vital signs: BP:107/69, R arm, HR: 68, RR 18, O2 Sat: 98% via room air, temp: 98.7, EKG: normal sinus. Client verbalized nausea and tremors have reduced but headache persists. Client refused to be transported to the hospital and left the observation area at 11:15 am.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tremor
Hospital-Tage
-
Labordaten
VS: 107/69, HR 68, RR 18, O2 98%, T: 98.7, Normal Sinus (EKG) and Blood Sugar: 93.
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
Penicillin
Vorherige Impfungen
-

VAERS 2110272

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
VA
Alter
60,0
Geschlecht
F
Eingang
14.02.2022
Impfdatum
12.01.2022
Beginn
22.01.2022
Tage bis Beginn
10,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Atrial fibrillation Cardioversion Chest pain Condition aggravated Device difficult to use Dizziness Dyspnoea Electrocardiogram normal Hyperhidrosis Magnetic resonance imaging heart

Symptomtext

10:00am: Sudden onset severe chest pain, shortness of breath, diaphoretic, lightheaded. 911 called. On monitor Rapid Afib heart rate of 220. Taken to ER by rescue squad. Difficulty inserting IV. On the way the ambulance hit a bumb & rate decreased to 140's afib, chest pain , diaphoresis, shortness of breath, lightheadedness subsided. Evaluated in ER at Hospital by cardiologist, Released home in "stable afib",, doubled flecainaide dose, hoping it will convert to sinus rythm over the weekend. To see cardiologist in office Monday. Monday AM approx 9:30am, had another epidode of chest pain, light headedness, diaphoresis. Cardiologist Dr said to meet him at hospital for a Cardioversion. Still remained in persistant symptomatic atrial fibrillation & was cardioverted on the 1st attempt under sedation, and was released from hospital in normal sinus rythm. Was told to stop taking flecainaide.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Mon, 1/24/22 Cardioverted for continuous symptomatic atrial fib Mon, 1/26/22 Follow up EKG with Dr Remains in NSR Fri. 1/28/22 referred to Dr cardiac electrophysiologist to discuss treatment plan. Tues 2/1/22 Heart MRI done
Aktuelle Erkrankungen
none
Vorgeschichte
controlled high blood pressure osteoarthritis reflux history of atrial fibrillation, corrected in 2019 with ablation, no episodes since (only rare instances of atrial tachycardia)
Andere Medikamente
atenolol flecainaide celebrex clonazapam prilosec zarelto synthroid multivitamin vitamin C zinc temazepam prn fioricet prn tramadol prn phendimetrazine,prn
Allergien
none
Vorherige Impfungen
Adverse effects after 2nd dose Moderna vaccine recieved 6/2/21 at Primary care physician office. Developed "Pulsatile tinnitus"

VAERS 2109120

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
PA
Alter
17,0
Geschlecht
F
Eingang
12.02.2022
Impfdatum
12.01.2022
Beginn
13.01.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest pain Cold sweat Dyspnoea Heart rate Heart rate increased Hyperhidrosis Pallor

Symptomtext

Chest pain (described as someone squeezing heart); Rapid heart rate; Shortness of breath; Sweating; Pale and clammy skin; Pale and clammy skin; This is a spontaneous report from a contactable reporter (Consumer or other non-HCP). The reporter is the patient. A 17 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in left arm, administration date 12Jan2022 at 15:30 (Lot number: FJ5683) at the age of 17 years as dose 1 (TRIS), single for COVID-19 immunisation. Relevant medical history included: "COVID-19" (unspecified if ongoing), notes: Prior to vaccination, was the patient diagnosed with COVID-19?:Yes. Concomitant medication included unspecified birth control medications. Past drug history included: Flu vaccine, for Immunisation, reaction: "Allergy to vaccine", notes: Known allergies : Flu vaccine. The following information was reported: CHEST PAIN (non-serious) with onset 13Jan2022 at 00:15, outcome "recovering", described as "Chest pain (described as someone squeezing heart)"; HEART RATE INCREASED (non-serious) with onset 13Jan2022 at 00:15, outcome "recovering", described as "Rapid heart rate"; DYSPNOEA (non-serious) with onset 13Jan2022 at 00:15, outcome "recovering", described as "Shortness of breath"; HYPERHIDROSIS (non-serious) with onset 13Jan2022 at 00:15, outcome "recovering", described as "Sweating"; PALLOR (non-serious), COLD SWEAT (non-serious), all with onset 13Jan2022 at 00:15, outcome "recovering", and all described as "Pale and clammy skin". Relevant laboratory tests and procedures are available in the appropriate section. The events "Chest pain (described as someone squeezing heart)", "Rapid heart rate", "Shortness of breath", "Sweating" and "Pale and clammy skin" were evaluated at the doctor or other healthcare professional office/clinic visit and emergency room visit. Therapeutic measures were taken as a result of chest pain, heart rate increased, dyspnoea, hyperhidrosis, pallor and cold sweat. Additional Information: The patient did not receive any other vaccines within four weeks prior to the COVID-19 vaccine. Prior to vaccination, the patient was diagnosed with COVID-19. Treatment included rest requirement for the events chest pain, heart rate increased, dyspnoea, hyperhidrosis, pallor and cold sweat. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Test Date: 20220113; Test Name: Heart rate; Result Unstructured Data: Test Result:Rapid heart rate; Comments: Time: 00:15.
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: COVID-19 (Prior to vaccination, was the patient diagnosed with COVID-19?:Yes.)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2109020

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NY
Alter
22,0
Geschlecht
F
Eingang
12.02.2022
Impfdatum
26.01.2022
Beginn
26.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Arrhythmia Heart rate Heart rate increased

Symptomtext

Arrhythmia; Heart rate 120 BPM; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 22 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 26Jan2022 18:00 (Lot number: FJ5683) at the age of 22 years as dose 3 (booster), single for covid-19 immunisation. The patient had no other medical history, no known allergies. The patient took concomitant medications, she received Birth control, Hippo Vegan Complete within 2 weeks of vaccination. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Vaccination history included: Bnt162b2 (Dose Number: 1, Batch/Lot No: ER8731, Location of injection: Arm Left), administration date: 14Apr2021, when the patient was 22 years old, for Covid-19 Immunization; Bnt162b2 (Dose Number: 2, Batch/Lot No: EP7533, Location of injection: Arm Left), administration date: 14May2021, when the patient was 22 years old, for Covid-19 Immunization. The patient was not pregnant when vaccination. Prior to vaccination, the patient was not diagnose with COVID-19. Since the vaccination, the patient has not been tested for COVID-19. The following information was reported: ARRHYTHMIA (medically significant) with onset 26Jan2022 20:00, outcome "not recovered", described as "Arrhythmia"; HEART RATE INCREASED (medically significant) with onset 26Jan2022 20:00, outcome "not recovered", described as "Heart rate 120 BPM". The events "arrhythmia" and "heart rate 120 bpm" were evaluated at the physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: heart rate: (26Jan2022) 120 BPM. Therapeutic measures were taken as a result of arrhythmia, heart rate increased, the treatment was given via IV. The case was reported as Non serious, No Results in death, No Life threatening, No Caused/prolonged hospitalization, No Disabling/Incapacitating, No Congenital anomaly/birth defect. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arrhythmia
Hospital-Tage
-
Labordaten
Test Date: 20220126; Test Name: Heart rate; Result Unstructured Data: Test Result:120 BPM
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: No known allergies: No
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2109002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NY
Alter
62,0
Geschlecht
F
Eingang
12.02.2022
Impfdatum
19.01.2022
Beginn
01.01.2022
Tage bis Beginn
-
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Abdominal pain Blood pressure measurement Blood urine present Dehydration Dry mouth Feeling abnormal Headache Hypersensitivity Nasal discomfort Pain Paraesthesia oral Renal haemorrhage Tinnitus

Symptomtext

kidneys started bleeding the next morning; blood in her urine; My lips are tingling; ringing in my ears; nasal passages were burning; allergic reaction; feel achy; tinges of headaches; abdominal aches; my mouth is so incredibly dry; I feel really emotional and cranky.; dehydration; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team for a Pfizer sponsored program . The reporter is the patient. A 62 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 19Jan2022 13:00 (Lot number: FJ5683) at the age of 62 years as dose 1, single for covid-19 immunisation. Relevant medical history included: "blood pressure was up" (unspecified if ongoing), notes: Consumer stated, "They said that my blood pressure was up, yes. They said when I had my blood pressure done. My blood pressure was 168 over 98."; "'28' of disc in my neck" (unspecified if ongoing), notes: I also take a pain medication because I have '28' of disc in my neck."; "pain" (unspecified if ongoing), notes: I also take a pain medication because I have '28' of disc in my neck."; "heart medication" (unspecified if ongoing), notes: I take Metoprolol which is a heart medication. Concomitant medication(s) included: METOPROLOL taken for cardiac disorder; BABY ASPIRIN. The following information was reported: RENAL HAEMORRHAGE (medically significant) with onset 20Jan2022, outcome "unknown", described as "kidneys started bleeding the next morning"; BLOOD URINE PRESENT (medically significant) with onset 20Jan2022, outcome "unknown", described as "blood in her urine"; PARAESTHESIA ORAL (non-serious) with onset Jan2022, outcome "unknown", described as "My lips are tingling"; TINNITUS (non-serious) with onset Jan2022, outcome "unknown", described as "ringing in my ears"; NASAL DISCOMFORT (non-serious) with onset Jan2022, outcome "unknown", described as "nasal passages were burning"; HYPERSENSITIVITY (non-serious) with onset Jan2022, outcome "unknown", described as "allergic reaction"; PAIN (non-serious) with onset Jan2022, outcome "unknown", described as "feel achy"; HEADACHE (non-serious) with onset Jan2022, outcome "unknown", described as "tinges of headaches"; ABDOMINAL PAIN (non-serious) with onset Jan2022, outcome "recovered", described as "abdominal aches"; DRY MOUTH (non-serious) with onset Jan2022, outcome "unknown", described as "my mouth is so incredibly dry"; FEELING ABNORMAL (non-serious) with onset Jan2022, outcome "unknown", described as "I feel really emotional and cranky."; DEHYDRATION (non-serious) with onset Jan2022, outcome "unknown", described as "dehydration". The events "kidneys started bleeding the next morning", "blood in her urine", "my lips are tingling", "ringing in my ears", "nasal passages were burning", "allergic reaction", "feel achy", "tinges of headaches", "abdominal aches", "my mouth is so incredibly dry", "i feel really emotional and cranky." and "dehydration" were evaluated at the physician office visit. The patient underwent the following laboratory tests and procedures: blood pressure measurement: 168 over 98, notes: They said that my blood pressure was up, yes. The caller had her first Pfizer Covid 19 vaccine 1st dose 19Jan. After getting the dose her kidneys started bleeding the next morning. She observed blood in her urine. Her doctor stated there is no infection. She has some concerns. Per caller: I have been having blood in my urine. They told me to drink a lot because the shot will dehydrate me. I drank water, cucumber water, and cranberry juice. I thought maybe it was a UTI and the doctor said I didn't have a UTI. It was right after the shot. I wasn't experiencing any pain in the abdomen. It seemed to go away. There was a day where there was no blood in the urine and then it returned. During the course of the night since I had the vaccination I wake up in the middle of the night and my mouth is so incredibly dry I have to drink two 20oz bottles of water. It's like the moisture is being zapped out of my body. My lips are tingling, ringing in my ears, nasal passages were burning. Almost like an allergic reaction. They did tell me I would feel achy, which I have been. But mentally I feel really emotional and cranky. I do get tinges of headaches, not full blown. I have noticed abdominal aches, like I always have to go to bathroom. I know the vaccine is new and the doctors don't know. What ingredient in this shot causes my body to be so dry? They told me the shot would cause dehydration. I thought I got rid of it when I started drinking the cranberry juice. I did see several times it was clear, there was no blood but then it came back today. When paraphrased, Consumer stated, "Yes and also there they did the doctor's office did took as no infection. It's not like I have a UTI. You know there was no bacteria. So, that's only the side effects from that was only thing different, put the shot and I do drink lot of water. I even drink cucumber water which is they said that the shot would dehydrate me. So, I was already drinking a lot of water but still had I mean you could see it was red in blood in the urine. So, there was no dyes or anything in the shot right? That would come up red in the urine. Yes they said that was one of the side effect that dehydration was one of the side effects and even was all the water that I am drinking I am still you know 'purifying' in my urine." When asked if the adverse event is ongoing : Consumer stated, "Well I have been treating it with cranberry juice and because I thought it might have been infection but and I drank more and more water, cucumber water I used cucumber water in my because they thought it might have been a UTI and it look like it was better for about a day and a half and then last night again it showed up again." Consumer stated, "I have been all drinking fluids they actually was looking to prescribe something but they called me today and they said it was there was no infection with this. It wasn't cause white infection." Therapeutic measures were taken as a result of renal haemorrhage, blood urine present. Therapeutic measures were not taken as a result of paraesthesia oral, tinnitus, nasal discomfort, hypersensitivity, pain, headache, abdominal pain, dry mouth, feeling abnormal, dehydration. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dehydration
Hospital-Tage
-
Labordaten
Test Name: blood pressure; Result Unstructured Data: Test Result:168 over 98; Comments: They said that my blood pressure was up, yes
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Blood pressure high; Cardiac disorder NOS (I take Metoprolol which is a heart medication); Discectomy (I also take a pain medication because I have '28' of disc in my neck."); Pain (I also take a pain medication because I have '28' of disc in my neck.")
Andere Medikamente
METOPROLOL; BABY ASPIRIN
Allergien
-
Vorherige Impfungen
-

VAERS 2108889

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NY
Alter
21,0
Geschlecht
M
Eingang
12.02.2022
Impfdatum
05.02.2022
Beginn
05.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood test Chest discomfort Dyspnoea Muscular weakness Pain in extremity Ultrasound scan

Symptomtext

Pain and weakness in the arm that the vaccine was given in. Shortness of breath and chest discomfort.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
Bloodwork and sonogram prescriptions written on 2/12/2022, patient referred to ER for the chest pain and discomfort.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2099908

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
TX
Alter
23,0
Geschlecht
F
Eingang
09.02.2022
Impfdatum
05.02.2022
Beginn
07.02.2022
Tage bis Beginn
2,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood test Chest pain Costochondritis Electrocardiogram X-ray

Symptomtext

I was diagnosed with costochondritis , I have a lot of stabbing on my left side in my chest that feel like a heart attack, it hurts all day every day and gets worsen at night to the point I cry myself to sleep.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
ekg , blood test and xray 2-8-22
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2099510

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CA
Alter
14,0
Geschlecht
M
Eingang
09.02.2022
Impfdatum
01.02.2022
Beginn
01.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Eye movement disorder Fall Joint contracture Tremor

Symptomtext

Pharmacist went over file and counseled patient on the vaccine and patient's parents stated that they understood but there was potentially some language barrier. Pharmacist administered the vaccine on 02/01 at approximately 4:25 PM and told patient and their parents that they need to sit and wait in the observation area for 15 minutes. Patient left to the front of the store before 15 minutes were over. Approximately 4:35 PM the pharmacy Store Manager saw the patient drop items that were going to be purchased at the front of the store and patient was on the ground held by his brother with tremors, hands clenching, and eyes rolled back. Pharmacist and 911 were called but patient refused to leave with 911 and patient's parents stated that it was not a seizure. No health conditions were reported on file or to paramedics. Patient left store and we have been unable to contact him or his parents since the event.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tremor
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
nothing was reported
Vorgeschichte
nothing was reported
Andere Medikamente
nothing was reported
Allergien
nothing was reported
Vorherige Impfungen
-

VAERS 2095805

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
GA
Alter
27,0
Geschlecht
F
Eingang
08.02.2022
Impfdatum
31.01.2022
Beginn
31.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Chest pain Dyspnoea Headache Nausea Pain Pyrexia

Symptomtext

Patient reported increased nausea & headaches beginning appx. 2 hours after injection. Condition worsened into fever, joint pain & aches, chest pain & shortness of breathing over the next several days. Fever has abated at time of reporting (8 days post injection), although, aches, pain & shortness of breath remain.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
genetic fatty liver disease; underactive thyroid
Vorgeschichte
symptomatic of Severe & Complex Developmental Trauma resulting in medically unexplained abdominal pain; headaches; nausea; joint pain; aches; back pain; racing heart; chest pain
Andere Medikamente
vitamin C; vitamin D; Probiotics; Milk Thistle; L-Theanine; Similace; Cortisol Manager; Ocella; Prozac; Levothyroxin; clonidine; gabapentin; Remeron
Allergien
amoxicillin; penicillin; doxycycline; stone fruits; red & green peppers; tomatoes; eggplant; rosemary; thyme; milk; citrus; green apples
Vorherige Impfungen
Pfizer EW0178 1st Dose COVID-19 Vaccine injected 5/28/2021 into left arm of Female age 27: resulted in chills; fatigue & aches.

VAERS 2093620

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
PR
Alter
15,0
Geschlecht
M
Eingang
07.02.2022
Impfdatum
15.01.2022
Beginn
17.01.2022
Tage bis Beginn
2,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Antipsychotic drug level Blood thyroid stimulating hormone Cyanosis Full blood count Lipids Metabolic function test Myocardial necrosis marker Palpitations Pyrexia Urine analysis Vitamin D

Symptomtext

Cianosis in nails (hands), palpitations. He took fever for 2 days 38.5 grades Celsius.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Palpitations
Hospital-Tage
-
Labordaten
CBC, CMP, U/A, TSH, VIT D, LITIUM, LIPID PANEL, CARDIAC ENZYMES AND TOMORROW IS GOING TO HIS APPOINTMENT WITH THE CARDIOLOGIST TO THE EKG AND ECOCARDIOGRAM.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2092091

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NJ
Alter
13,0
Geschlecht
M
Eingang
07.02.2022
Impfdatum
08.01.2022
Beginn
28.01.2022
Tage bis Beginn
20,0
Dosis
3
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein
Back pain Bacterial test negative Blood creatine phosphokinase normal Borrelia test negative C-reactive protein normal Chest pain Differential white blood cell count normal Full blood count normal Gait disturbance Hypoaesthesia Magnetic resonance imaging spinal normal Metabolic function test normal Muscle spasms Neurological examination abnormal Pain Pain in extremity Paraesthesia Red blood cell sedimentation rate normal

Symptomtext

1/28/22 (20 days following receipt of 3rd dose of Pfizer mRNA vaccine) vaccinee abruptly developed lower thoracic-upper lumbar back/spine pain with radiation of pain to both lower extremities, numbness/pins and needles in both lower extremities and antalgic gait

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Evaluated in Medical Center ED on 1/28/22 and 1/30/22. MRI with/without contrast of mid-thoracic-lumbar spine wnl (without evidence of myelitis, vertebral body or disc abnormalities). Evaluation by neurologist did not reveal any focal neurological deficit; examination revealed only paraspinal muscle spasm. Laboratory tests (CBC/diff, CMP, ESR, CRP, CK) all wnl. Serology for B. burgdorferi, E. chaffeensis, A. phagocytophilum, B. microti all negative.. Patient in process of seeking evaluation from another neurologist.
Aktuelle Erkrankungen
Surgical transposition of right ulnar nerve (12/21)
Vorgeschichte
asthma recurrent sinusitis
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2091312

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
VA
Alter
60,0
Geschlecht
F
Eingang
05.02.2022
Impfdatum
12.01.2022
Beginn
22.01.2022
Tage bis Beginn
10,0
Dosis
1
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Atrial fibrillation Heart rate Hyperhidrosis Hypotension SARS-CoV-2 test

Symptomtext

rapid atrial fibrillation; chest pain and HR 220; diaphoretic; hypotension; This is a spontaneous report received from contactable reporter via COVID-19 Vaccine Adverse Event Self-Reporting Solution portal. The reporter is the patient. A 60 year-old female patient (not pregnant) received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection), administered in arm left, administration date 12Jan2022 15:00 (Lot number: FJ5683) at the age of 60 years as dose 1, single for COVID-19 immunization. The facility where the most recent COVID-19 vaccine was administered was at the hospital. Relevant medical history included: "former history of atrial fibrillation (fib)," start date: 2019 (unspecified if ongoing), notes: prior to ablation 3 years prior reporting (completely controlled after ablation); "ablation" (unspecified if ongoing); "hypertension (HTN)" (unspecified if ongoing). The patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. The patient took other unspecified concomitant medications within 2 weeks of vaccination. The following information was reported: ATRIAL FIBRILLATION (medically significant, life threatening) with onset 22Jan2022 09:30, outcome "not recovered," described as "rapid atrial fibrillation; chest pain and heart rate (HR) 220"; HYPERHIDROSIS (life threatening) with onset 22Jan2022 09:30, outcome "not recovered," described as "diaphoretic"; HYPOTENSION (life threatening) with onset 22Jan2022 09:30, outcome "not recovered," described as "hypotension." The events "rapid atrial fibrillation; chest pain and HR 220," "diaphoretic," and "hypotension" were evaluated at the emergency room visit. The patient underwent the following laboratory tests and procedures: HR: (22Jan2022) 220 and Nasal Swab: (22Jan2022) negative. Therapeutic measures were taken as a result of atrial fibrillation, hyperhidrosis, and hypotension, which included rescue squad, intravenous (IV) fluids, and medication.; Sender's Comments: Based on available information and known product profile, the causal relationship between the reported events and the use of BNT162B2 cannot be fully excluded. However, the history of atrial fibrillation is confounding. 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
Hypotension
Hospital-Tage
-
Labordaten
Test Date: 20220122; Test Name: HR; Result Unstructured Data: Test Result:220; Test Date: 20220122; Test Name: Nasal Swab; Test Result: Negative
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Atrial fibrillation (prior to ablation 3 years ago (completely controlled after ablation)); Cardiac ablation; Hypertension
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2091270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
-
Alter
61,0
Geschlecht
F
Eingang
05.02.2022
Impfdatum
21.01.2022
Beginn
01.01.2022
Tage bis Beginn
-
Dosis
3
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Dysphagia Dyspnoea Hypoaesthesia oral Throat tightness Vaccination site erythema

Symptomtext

throat felt like it was closing up; her lips started to get numb; hard to swallow; hard to breath; she got a little red dot at the injection site, in the left arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 21Jan2022 (Lot number: FJ5683) at the age of 61 years as dose 3 (booster), single for covid-19 immunisation; diphenhydramine hydrochloride (BENADRYL), since 21Jan2022 (Batch/Lot number: unknown) at pill. Relevant medical history included: "allergy to corn" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: Bnt162b2 (Second dose, EW0183), administration date: 15May2021, when the patient was 60 years old, for Covid-19 immunization, reaction(s): "allergic reaction"; Bnt162b2 (First dose, LOT-EW0151), administration date: 02Apr2021, when the patient was 60 years old, for Covid-19 immunization, reaction(s): "allergic reaction". The following information was reported: THROAT TIGHTNESS (non-serious) with onset 21Jan2022, outcome "unknown", described as "throat felt like it was closing up"; HYPOAESTHESIA ORAL (non-serious) with onset 21Jan2022, outcome "unknown", described as "her lips started to get numb"; DYSPHAGIA (non-serious) with onset 21Jan2022, outcome "unknown", described as "hard to swallow"; DYSPNOEA (non-serious) with onset 21Jan2022, outcome "unknown", described as "hard to breath"; VACCINATION SITE ERYTHEMA (non-serious) with onset Jan2022, outcome "unknown", described as "she got a little red dot at the injection site, in the left arm". The event "hard to breath" was evaluated at the emergency room visit. Therapeutic measures were taken as a result of dyspnoea. Additional information: This report is not related to a study or programme. Other products was not provided. The patient taking Benadryl pre treatment for vaccine. Reporter seriousness for given Benadryl 30 minutes prior to vaccine and it did not work was unspecified. On 21Jan2022 nurse there gave her a pill of the Benadryl, waited 30 minutes and it did not work. Caller states the nurse got it from the pharmacy there, states the bottle had not been opened. Lot and Expiration was unknown. Patient history was not provided. Investigation assessment not provided. It was reported hard to breathe, states they immediately wheeled her to the urgent care and was there for 2.5 hours, states she treated with a breathing treatment in urgent care, did not give her prednisone because the doctor said that would interfere with the vaccine. Her eyes are brown. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Food allergy
Andere Medikamente
BENADRYL
Allergien
-
Vorherige Impfungen
-

VAERS 2091106

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
VA
Alter
49,0
Geschlecht
F
Eingang
05.02.2022
Impfdatum
28.01.2022
Beginn
28.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Hypoaesthesia Lymphadenopathy Oedema Oedema peripheral Pain in extremity Paraesthesia

Symptomtext

Severe edema of left arm and left breast, axillary and subclavicular lymphadenopathy. Left arm pain, left shoulder pain, numbness and tingling in left upper extremity. No significant improvement after 6-day steroid dose pack.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Hypertension, GERD
Andere Medikamente
HCTZ, Omeprazole
Allergien
-
Vorherige Impfungen
-

VAERS 2085213

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
PR
Alter
57,0
Geschlecht
F
Eingang
03.02.2022
Impfdatum
13.01.2022
Beginn
14.01.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Condition aggravated Pruritus Rash

Symptomtext

On January 13, the third dose of Pfizer was administered to the patient and she present rash and itching in both upper limbs even taking Atarax and Claritin. The patient had presented the same thing in the second dose and was evaluated by the dermatology Doctor which ordered him to take Atarax and Claritin.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Condition aggravated
Hospital-Tage
-
Labordaten
No
Aktuelle Erkrankungen
Hypertension
Vorgeschichte
No
Andere Medikamente
Atarax and Claritin
Allergien
Aspirin
Vorherige Impfungen
Yes. When getting the Second dose of the Covid-19 Pfizer vaccine was when I first started with the rash on body.

VAERS 2082564

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NY
Alter
42,0
Geschlecht
F
Eingang
02.02.2022
Impfdatum
02.02.2022
Beginn
02.02.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chest pain Electrocardiogram normal Injection site pain Interchange of vaccine products Pain

Symptomtext

42yo F px with no PMH, here to receive the Pfizer booster after receiving Johnson & Johnson as a primary vaccine. Approx. 7min after the shot she felt pain in the right arm (Injection site) that was radiating to the right side of her chest, sharp, 7/10, exacerbated by arm movement and alleviated by leaving the arm still. Denied any other symptom. Patient was evaluated by on-site EMS and MD. On PE AAO x 3; Initial VS: HR 82, RR 18, SpO2 99%, BP 118/74. RRR, lungs CTA, normal ROM on the affected limb. EKG (normal sinus rhythm); After 30min observation she felt better, pain now 2/10. Repeated set of VS WNL. Advised to go to the hospital to get a complete evaluation, but she refused. She was d/c home.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2074907

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FJ5683

moderat
Staat
SC
Alter
56,0
Geschlecht
F
Eingang
30.01.2022
Impfdatum
18.05.2021
Beginn
21.05.2021
Tage bis Beginn
3,0
Dosis
1
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein
Arthralgia Magnetic resonance imaging normal Migraine Muscular weakness

Symptomtext

Severe joint pain and weakened mucles migraines

Weitere VAERSDATA-Felder
Praegender Schweregrund
Migraine
Hospital-Tage
-
Labordaten
Had mri thought i had pinched nerve mri was clear
Aktuelle Erkrankungen
No illness
Vorgeschichte
Extreme pain in all joints and muscle weakness had mri thought maybe pinched nerve it was clear
Andere Medikamente
Aleve
Allergien
None
Vorherige Impfungen
-

VAERS 2072163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CA
Alter
63,0
Geschlecht
M
Eingang
28.01.2022
Impfdatum
28.01.2022
Beginn
28.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Hypoaesthesia Injection site paraesthesia Palpitations Vertigo

Symptomtext

During observation, at the 30 minute mark, patient reported having numbness on the right arm, tingling on the left arm injection site, heart palpitation, and vertigo. Patient was placed in reclined position and offered water. After laying down for 20 minutes, patient reported no more heart palpitation, the numbness went away, and the vertigo was improved.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site paraesthesia
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
multi-vitamins, zinc supplements, vitamin C, vitamin D3, CoQ10, iron supplement, biotin
Allergien
none
Vorherige Impfungen
vertigo at age 62, after pfizer #1 on 1/15/2021

VAERS 2071655

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NY
Alter
34,0
Geschlecht
F
Eingang
28.01.2022
Impfdatum
27.01.2022
Beginn
27.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chest discomfort Dyspnoea

Symptomtext

PT HAD DIFFICULTY BREATHING, CHEST TIGHTNESS AFTER INJECTION. PT TRANSPORTED TO EMERGENCY DEPARTMENT

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dyspnoea
Hospital-Tage
-
Labordaten
UNKNOWN
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
ALLEGRA 180MG ZYRTEC 10MG AT NIGHT, MONTELUKAST 10MG EVERY NIGHT. ALBUTEROL (PROAIR, VENTOLIN) 2 PUFFS EVERY 4-6 HOURS AS NEEDED FOR COUGH/WHEEZE OR DIFFICULTY BREATHING 2 HOURS PRIOR TO COVID VACCINE PREDNISONE 30MG BY MOUTH. 1HR PRIOR TO
Allergien
N/A
Vorherige Impfungen
-

VAERS 2062229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NY
Alter
60,0
Geschlecht
F
Eingang
25.01.2022
Impfdatum
24.01.2022
Beginn
24.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Headache Hypertension Pain Pain in extremity

Symptomtext

Patient reporting dizziness, feeling lasted about 3 minutes, High blood pressure, body aches, headaches, and sore arm.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypertension
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Wellbutrin, Dextral
Allergien
Morphine, Penicillin
Vorherige Impfungen
-

VAERS 2058245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CA
Alter
17,0
Geschlecht
M
Eingang
23.01.2022
Impfdatum
18.01.2022
Beginn
23.01.2022
Tage bis Beginn
5,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Back pain Chest X-ray Chest pain Chills Dyspnoea Electrocardiogram Headache Laboratory test Muscle spasms Nausea Tremor

Symptomtext

Chest pains was experienced suddenly around 4:25 pm today while walking dog. This was accompanied by breathing problem and extreme lower back pain. This subsided after few minutes. Then nausea and headache came. Patient walked back to car with me and after 10 min, complained of chest spasms and an uncontrollable chill and shaking occurred for few minutes which led me to call his doctor's office where a nurse advised me to take him to ER.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
Tests being conducted at present inc chest xray, blood labs and EKG.o
Aktuelle Erkrankungen
None
Vorgeschichte
Congenital adrenal hyperplasia
Andere Medikamente
Dexamethesone, fludrocort
Allergien
None
Vorherige Impfungen
MMR, leg weakness, 11?

VAERS 2057729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CA
Alter
43,0
Geschlecht
M
Eingang
22.01.2022
Impfdatum
22.01.2022
Beginn
22.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Flushing Pain in extremity Tachycardia Throat irritation

Symptomtext

About 8 minutes post injection, patient became extremely flushed, tachycardic, had pain in left arm and itchiness around the throat. Paramedics were called and transported patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tachycardia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2057608

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CA
Alter
23,0
Geschlecht
F
Eingang
22.01.2022
Impfdatum
14.01.2022
Beginn
14.01.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Anxiety Asthenia Chest discomfort Cold sweat Emotional distress Erythema Flushing Hypoaesthesia Paraesthesia Peripheral coldness Skin warm

Symptomtext

Patient received Pfizer Vaccine at 3:40pm, then sat for 15 minutes and left the clinic. Patient returned at 4:45pm to clinic and stated while she was driving she felt very anxious and felt tingling/numbness left arm to her hand opposite of her injection site. She stated chest tightness and pressure and felt very warm. Offered water and snacks since patient's last meal was at 10am this morning. Took first set of vitals: HR 87, Temp 97.8F, SpO2 100% at room air. Offered instant ice pack. Patient sat down for 10 minutes and proceeded to lay down on the cot because she felt weak. patient was very anxious and distressed. Stated her symptoms were not improving. Denies any previous medical history or allergies to medications. Stated she did not taken any medicaitons within 12 hours. Stated she had chest tightness similar to previous covid infection. Patient started closing her eyes and had visible eye tremors. Hands were cold and clamy. Face was flushed and red. she stated she had chest tightness and denies chest pain. Patient stated she had previous chest tightness due to previous covid19 infection. Clinic called 911 and fire department arrived on scene. Fire department provided vital signs; 12 lead : sinus rhythm no stemi, HR 80, RR 20, BP 148/100, SpO2 90%. Patient decided to go to ER with friend instead of going with paramedics .

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2054547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
-
Alter
22,0
Geschlecht
M
Eingang
21.01.2022
Impfdatum
10.01.2022
Beginn
10.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Chest pain Pain

Symptomtext

Primary series w/ other vaccine manufacturer Pt reported 1-4-5 rating of intermittent pain left lateral mid chest pain that began while sitting after vaccine. Pt states that it may be the way he slept. Vitals: 14:03 103/73, 67, 12, 97.3F, 100% -- > 14:08 105/63, 65, 12 Pt stable and released from the vaccination site. Recommended that pt f/u w/ PCP. Call 911 or go to ER is pain increases of pt develops SOB. Pt stable and released from the vaccination site.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Unknown
Andere Medikamente
Unknown
Allergien
None
Vorherige Impfungen
-

VAERS 2052300

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CA
Alter
37,0
Geschlecht
M
Eingang
20.01.2022
Impfdatum
18.01.2022
Beginn
20.01.2022
Tage bis Beginn
2,0
Dosis
3
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Burning sensation Chills Pain Pyrexia Tachycardia Vomiting

Symptomtext

15 hours post 3rd vaccination, the following symptoms appeared: Fever; T: 102.5; intense chills (approximately 15 min) with tachycardia (144 bpm max) without fever; vomiting; joint pain/burning sensation and body aches. Tylenol used to relieve fever. Advil used to relieve body aches and joint pain.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tachycardia
Hospital-Tage
-
Labordaten
N/A.
Aktuelle Erkrankungen
COVID-19 positive December 29, 2021 with very mild symptoms.
Vorgeschichte
None
Andere Medikamente
None
Allergien
Latex
Vorherige Impfungen
Pfizer-BioNTech 2nd Dose.

VAERS 2052297

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CA
Alter
43,0
Geschlecht
M
Eingang
20.01.2022
Impfdatum
13.01.2022
Beginn
14.01.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Cold sweat Head discomfort Hyperhidrosis Hypertension Joint stiffness Lymphadenopathy Myalgia Palpitations Pyrexia

Symptomtext

Fever of 104.6, sweating, muscle pain, joint stiffness, swollen lymph nodes, pressure in the head, racing heart rate, and elevated blood pressure. After taking Ibuprofen, temperature went down to 96.6 with cold sweat.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypertension
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2039616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
NJ
Alter
60,0
Geschlecht
F
Eingang
17.01.2022
Impfdatum
10.01.2022
Beginn
10.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood test Diarrhoea Mobility decreased Pain in extremity Pyrexia

Symptomtext

Arm was very sore and difficult to remove. She also had a fever and diarrhea.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Mobility decreased
Hospital-Tage
-
Labordaten
yes blood work
Aktuelle Erkrankungen
no
Vorgeschichte
no
Andere Medikamente
armour 30mcg
Allergien
penicillin
Vorherige Impfungen
arm was swollen for 6wks and they where bruise black and blue

VAERS 2036100

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CA
Alter
21,0
Geschlecht
F
Eingang
14.01.2022
Impfdatum
14.01.2022
Beginn
14.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Anxiety Erythema Interchange of vaccine products Pruritus Tachycardia

Symptomtext

21-year-old woman with h/o CNS 1, stage III B cell lymphoblastic lymphoma s/p treatment. She recently completed treatment. She has received the Jansen vaccine in the past. Of note, she had a h/o anaphylaxis to PEG asparaginase. She has been cleared by her allergist to receive the Pfizer vaccine. Today, she presents for her second dose (first Pfizer dose). Patient tolerated vaccine well. No immediate anaphylactic response. She was monitored on continuous pulse ox for 45-50 minutes. Serial vitals were taken. One instance of tachycardia to 120 associated with anxiety, otherwise completed asymptomatic. No other vital sign abnormalities. At 1122, patient reported mild itching along back. Back carefully examined. A small quarter sized erythema was noted left upper spine. Back, chest, abdomen, legs did not have any notable rashes or concerns. Given known medical history, h/o anaphylaxis, one dose of PO 25 mg Benadryl capsule was administered. Mother and patient did not wish to take 50mg given dose strength, despite weight of 49.9 kg. Patient was monitored for an additional 10-15 minutes. Small area of erythema completely gone/resolved following medication. Body was further examined and no additional erythema, rash, itching was present. Airway was examined again, there was not notable angioedema, tongue/lip/oral cavity swelling. Patient reports feeling well without any symptoms. No more itching.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tachycardia
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
CNS 1 stage III B-cell lymphoblastic lymphoma
Vorgeschichte
CNS 1 stage III B-cell lymphoblastic lymphoma
Andere Medikamente
Benadryl 25 mg PO capsule
Allergien
asparaginase PEG. E. Coli, platelets, amoxicillin, palononsetron
Vorherige Impfungen
-

VAERS 2032846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CO
Alter
53,0
Geschlecht
F
Eingang
13.01.2022
Impfdatum
01.01.2022
Beginn
11.01.2022
Tage bis Beginn
10,0
Dosis
3
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal pain Arthralgia Diarrhoea Fatigue Feeding disorder Headache Pain Paraesthesia oral Pyrexia

Symptomtext

Booster shot after J& J 1/11- Felt tingling in lips 10 minutes after shot. I could smell the medicines and taste them in my mouth. Diarrhea started at 3:00, fever soon after. Starting on 1/11 4:30 pm, Fever and All of my joints from my jaw down to my fingertips and toes were in fire and stinging, lasting until 10:00 am on 1/12. Severe headache throughout. Pure exhaustion and not functioning until 10:00 on 1/13. Not able to eat from 1/11 1:00 pm until 1/13 1:30 pm, wicked belly pains once I?ve eaten as well. I really thought I might die, it was horrible.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia oral
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Penicillan
Vorherige Impfungen
J&J 5/23 - 3 day fever and horrible aches and headaches

VAERS 2031964

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
PR
Alter
17,0
Geschlecht
F
Eingang
13.01.2022
Impfdatum
13.01.2022
Beginn
13.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Hyperhidrosis Nausea Paraesthesia

Symptomtext

Patient refers dizziness, paresthesias, diaphoresis and nausea after receiving the Pfizer COVID vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
V/S WNL (INITIAL) BP:120/80 P: 70 T: 36.1 O2%: 95 V/S WNL (30 MIN REEVALUATION): BP: 120/80, P: 69, T: 36.5, O2%: 94
Aktuelle Erkrankungen
NKDA
Vorgeschichte
Brachial Plexus Paralysis, Asma, Epilepsy
Andere Medikamente
N/A
Allergien
PCN
Vorherige Impfungen
-

VAERS 2028834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

moderat
Staat
CA
Alter
39,0
Geschlecht
F
Eingang
12.01.2022
Impfdatum
12.01.2022
Beginn
12.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Asthenia Dizziness Dysgeusia Dysstasia Headache Hypertension Nausea Neurological examination normal Retching

Symptomtext

Signed Hide copied text Hover for details Patient developed dry heaving, nausea, sever headache, metallic taste almost immediately after she received the COVDI vaccine Pfizer booster. BP 155/111 FA HER 66, O2 saturation 100% . She denied any chest pain, shortness of breath, chest pain, heart palpitation, numbness or weakness in her extremities. Neuro exam wnl. Emergency medication including epi was offered by charge Nurse, however patient declined. Patient was observed over an hour period. Given persistent throbing headache, high bp, overall weakness and patients inability to stand still due to lightheadedness, emergency was notified. Patient was safely transferred by parametics ambulance to ER. Additional vitals 154/104, 147/97, 155/111, HR 60's-70's O2 Sat 100%

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypertension
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
no
Vorgeschichte
no
Andere Medikamente
none
Allergien
penicillin, Vicodin
Vorherige Impfungen
-

VAERS 2028444

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
CA
Alter
44,0
Geschlecht
F
Eingang
12.01.2022
Impfdatum
12.01.2022
Beginn
12.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Hypoaesthesia Paraesthesia

Symptomtext

NUMBNESS & TINGLING OF RIGHT ARM AND HAND WITH RADIATION TO RIGHT LEG AND RIGHT FOOT/GREAT TOE

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
HASHIMOTO THYROIDITIS, CHRONIC BACK PAIN, FIBROMYALGIA, IMPLANTED NERVE STIMULATOR
Andere Medikamente
-
Allergien
CIOROFLOXACIN, DECADRON, IMITREX, DEMEROL, LATEX, MORPHINE, AZITHROMYCIN,OXYCODONE, ONION, SULFA
Vorherige Impfungen
-

VAERS 2025747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

moderat
Staat
PA
Alter
17,0
Geschlecht
F
Eingang
11.01.2022
Impfdatum
04.01.2022
Beginn
11.01.2022
Tage bis Beginn
7,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Dizziness postural Electrocardiogram Injection site bruising Injection site haemorrhage Injection site swelling Muscular weakness Pallor Paraesthesia Vertigo Vision blurred

Symptomtext

Very bloody injection site, dime size bruising and bump, seen for vertigo/dizziness 01/11/2022 felt faint, dizzy, pale skin 4:15pm at lacrosse practice-this never happened before. Reports legs felt wobbly and tingly. Vision fuzzy Coach made her sit, trainer examined her. She remained pale so sent her down the hall to urgent care.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Paraesthesia
Hospital-Tage
-
Labordaten
Blood pressure, pulse ox, pulse, listen to heart & breathing, ECG, Vertigo tests Still feel slightly dizzy upon standing
Aktuelle Erkrankungen
None
Vorgeschichte
seasonal allergies, exercise induced asthma
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2613200

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
TX
Alter
59,0
Geschlecht
F
Eingang
11.04.2023
Impfdatum
10.04.2022
Beginn
03.07.2022
Tage bis Beginn
84,0
Dosis
4
Route/Site
SYR / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood test normal COVID-19 Cough Fatigue Inflammation Malaise Pyrexia Rash Rash erythematous Rash pruritic Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Skin discolouration Vasculitis

Symptomtext

My COVID-19 symptoms started on 07/03/2022. I had fever, cough, runny nose, fatigue, and congestions. I did home COVID-19 test on 07/04/2022 which was negative. On 07/05/2022 I did another COVID-19 home test which was positive. I did a telehealth with PA from my doctor's office who prescribed me intravenous monoclonal infusion. On 03/2023 I noticed rash on my leg. It was a red, inflamed and itching between my knee and ankle on my left leg. The redness started to look purple so I went to my doctor. The doctor wasn't sure what it was. We did all kinds of blood work which was normal. He said it Vasculitis. He gave me an steroid cream. I still have fatigue but other symptoms are gone. I still have the rash when I touch it itches. It's getting better but very slowly.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
05JUL2022 COVID-19 test positive
Aktuelle Erkrankungen
Seasonal Allergies
Vorgeschichte
High Blood Pressure; Seasonal Allergies
Andere Medikamente
Lisinopril; vitamin D; vitamin B12; ALLEGRA; multivitamins
Allergien
Tetracycline
Vorherige Impfungen
-

VAERS 2588575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NY
Alter
62,0
Geschlecht
F
Eingang
28.02.2023
Impfdatum
24.02.2022
Beginn
22.11.2022
Tage bis Beginn
271,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Cough Influenza virus test Malaise Nasal congestion SARS-CoV-2 test Streptococcus test Viral infection

Symptomtext

My nose was clogged up and I was coughing and I was not feeling well. I went into my doctor and I was told I had viral infection. I was given a Z-PAK, and really just had to wait it out. I struggled with the clogged nose and the cough and using OTC medications to help get over it.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Malaise
Hospital-Tage
-
Labordaten
COVID-19 PCR test; Influenza test; Strep test
Aktuelle Erkrankungen
N/A
Vorgeschichte
Pre-Diabetic
Andere Medikamente
Calcium; potassium chloride; budesonide nasal spray
Allergien
Penicillin
Vorherige Impfungen
-

VAERS 2535368

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
MA
Alter
68,0
Geschlecht
F
Eingang
16.12.2022
Impfdatum
27.01.2022
Beginn
27.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Asthenia Dizziness Immediate post-injection reaction Inflammation Joint range of motion decreased Loss of personal independence in daily activities Pain Pain in extremity

Symptomtext

pt states that she felt dizzy and nauseated immediately after getting the vax. Within 24 hours her left arm became sore and she experienced weakness. She lost range of motion and had to see her PCP. She was referred to have physical therapy. After several months of physical therapy with no improvement was then referred to an orthopedic Dr. She was given a cortisone injection. She was told this was from having inflammation from the vaccine. She states she has had improvement after having this injection but still some achiness and some limitations. Her arm is about 80-90% better at this time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
autoimmune inflammatory disease (possible MS)
Andere Medikamente
none
Allergien
green mango iodine
Vorherige Impfungen
-

VAERS 2499379

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
SC
Alter
72,0
Geschlecht
F
Eingang
04.11.2022
Impfdatum
04.05.2022
Beginn
04.05.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthritis Bone pain Gait disturbance Myalgia Pain Pain in extremity Spinal X-ray abnormal Walking aid user X-ray of pelvis and hip abnormal

Symptomtext

The evening when I had the vaccination when I went to bed, I had extreme pain going down through my whole body. My muscles and bones all the way down to my toes. I've never had anything like that before except when I had COVID-19, but it wasn't as severe at the time. This was a severe pain. This went on for 8-10 hours that evening. I have arthritis on the right side of my body with my right hip. I was walking with a limp at the time, and that has gotten worse. I wasn't sure if this was in relation to the vaccine or not. It's gotten to the point where by the end of September, I could hardly walk due to the problems with my right side. I was walking with a cane and it was still difficult to walk. I finally went to an orthopedic doctor and he prescribed physical therapy and it has helped, but it's still painful to walk. The only thing that changed was getting the vaccine prior to these health events occurring. I would say it has gotten a bit better, but I still have a ways to go with recovery.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bone pain
Hospital-Tage
-
Labordaten
X-ray of back and hips, indicated arthritis.
Aktuelle Erkrankungen
None
Vorgeschichte
Mild Asthma; Migraines; Arthritis
Andere Medikamente
TYLENOL; SINGULAIR; ESTRACE; fluticasone propionate inhaler
Allergien
Mold
Vorherige Impfungen
Pneumonia vaccine 2019, arm was swollen and ached for a week.

VAERS 2497169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NH
Alter
62,0
Geschlecht
F
Eingang
03.11.2022
Impfdatum
28.01.2022
Beginn
28.09.2022
Tage bis Beginn
243,0
Dosis
4
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Body temperature Body temperature increased COVID-19 Delirium Dizziness Fatigue Pain in extremity

Symptomtext

sore arm; Fatigue; Kind of delirious; dizzy; Temperature 102. 9; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient received BNT162b2 (BNT162B2), in morning on 28Jan2022 as dose 4 (booster), single (Lot number: FJ5683) at the age of 62 years intramuscular, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Arrhythmia" (unspecified if ongoing); "Arthritis" (unspecified if ongoing). Concomitant medication(s) included: METOPROLOL oral taken for arrhythmia (ongoing); MELOXICAM oral taken for arthritis, start date 05Sep and stop date 06Sep. Vaccination history included: BNT162b2 (Dose: 3rd, Date/time:, Date: 31Aug2021, Time: morning, Site and route of injection:, Anatomical site of injection: arm (Left), Route of administration: Intramuscular, Batch/lot number: FA6780), administration date: 31Aug2021, when the patient was 62-year-old, for Covid-19 immunization, reaction(s): "sore arm", "Fatigue"; BNT162b2 (Dose: 2nd, Date/time:, Date: 15Apr2021, Time: morning, Site and route of injection:, Anatomical site of injection: arm (Left), Route of administration: Intramuscular, Batch/lot number: EW0161), administration date: 15Apr2021, when the patient was 62-year-old, for Covid-19 immunization, reaction(s): "sore arm", "Fatigue"; BNT162b2 (Dose: 1st, Date/time:, Date: 05Mar2021, Time: Morning , Site and route of injection:, Anatomical site of injection: arm (Left), Route of administration: Intramuscular, Batch/lot number: EN6207), administration date: 05Mar2021, when the patient was 62-year-old, for Covid-19 immunization, reaction(s): "sore arm", "Fatigue". The following information was reported: DELIRIUM (medically significant) with onset 28Sep2022, outcome "unknown", described as "Kind of delirious"; BODY TEMPERATURE INCREASED (non-serious) with onset 28Sep2022, outcome "unknown", described as "Temperature 102. 9"; DIZZINESS (non-serious) with onset 28Sep2022, outcome "unknown", described as "dizzy"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "sore arm"; FATIGUE (non-serious), outcome "unknown". The patient underwent the following laboratory tests and procedures: Body temperature: (28Sep2022) 102. 9 Fahrenheit, notes: Norm Low: 98.6, Norm High: 98.6, Kind of delirious, dizzy; COVID-19: (08Sep2022) positive, notes: I continue to test positive. Clinical course: The patient stated she had no adverse events associated with any of my vaccine, just sore arm plus fatigue for one day.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
Test Date: 20220928; Test Name: temperature; Result Unstructured Data: Test Result:102. 9 Fahrenheit; Comments: Norm Low: 98.6 Norm High: 98.6 Kind of delirious, dizzy; Test Date: 20220908; Test Name: Covid-19; Test Result: Positive ; Comments: I continue to test positive
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Arrhythmia; Arthritis
Andere Medikamente
METOPROLOL; MELOXICAM
Allergien
-
Vorherige Impfungen
-

VAERS 2486906

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
TX
Alter
67,0
Geschlecht
M
Eingang
24.10.2022
Impfdatum
18.04.2022
Beginn
10.08.2022
Tage bis Beginn
114,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Chest discomfort Cough Pyrexia Respiratory tract congestion SARS-CoV-2 test

Symptomtext

About four months after receiving my fourth dose (second booster) of Pfizer, I contracted COVID-19. I was experiencing congestion, tightness in my chest and a low-grade fever. When I went to my local clinic, I waited in the parking lot where they came out and tested me. The doctor gave me Paxlovid. My symptoms never got worse, and they went away within a few days. I did have the persistent cough for a few weeks, but it went away after a little while.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
COVID-19
Aktuelle Erkrankungen
None
Vorgeschichte
High Cholesterol; High Blood Pressure
Andere Medikamente
Quinapril; Simvastatin; Fish Oil; Co-Q-10; Vitamin D; Probiotic
Allergien
Penicillin
Vorherige Impfungen
-

VAERS 2465501

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
LA
Alter
61,0
Geschlecht
F
Eingang
30.09.2022
Impfdatum
30.03.2022
Beginn
25.09.2022
Tage bis Beginn
179,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Exposure to SARS-CoV-2 Malaise SARS-CoV-2 test positive

Symptomtext

Contracted COVID 19 . Exposed on 9/20/22. Tested positive on 9/25/22 when symptoms appeared. Paxlovid prescribed.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Malaise
Hospital-Tage
-
Labordaten
Home test 9/24/22- negative 9/25/22 - positive 9/26/22- positive Paxlovid prescribed.
Aktuelle Erkrankungen
N/A
Vorgeschichte
Neuropathy from West Nile Virus, Osteoarthritis, High Blood Pressure, Diabetes Type 2 , Hyperlipidemia, Carpel Tunnel Syndrome
Andere Medikamente
Aspirin, Claritin , Vitamin s B12, C & D3, Omega 3?s, Glucosamine MSM, Celecoxib, Metformin, Pregabalin, Lisinopril, Atorvastatin , Magnesium.
Allergien
N/A
Vorherige Impfungen
-

VAERS 2459733

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
TX
Alter
62,0
Geschlecht
F
Eingang
24.09.2022
Impfdatum
17.01.2022
Beginn
18.01.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: ja Erholt: nein
Atrioventricular block complete Blood test Cardiac monitoring Cardiac pacemaker insertion Dizziness Electrocardiogram abnormal Laboratory test Magnetic resonance imaging Sluggishness

Symptomtext

Received injection and went home. Was feeling a little sluggish that evening, but I didn?t think anything about it. The morning of January 19, 2022 at approximately 9:15 a.m., I had just left my house on foot to walk my 16 year old. I had walked approximately 80 meters and almost immediately felt light headed and dizzy. I immediately returned to home, took my blood pressure and my heart rate was 40. I monitored my heart rate for approximately 45 minutes, using two separate heart rate monitors; with only slightly different readings. I called for my husband to come inside the house and he took me to the hospital. Once at the hospital, I was taken by wheelchair to an exam room where the nursing staff immediately executed a 12 lead ECG and I was diagnosed to a ?TOTAL AV BLOCK? and was being sent to the Cardiac unit at Medical Center.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
2,0
Labordaten
ECG, MRI, various blood tests and most likely tests that could be verified by the insurance claim. Pacemaker implanted on January 1/20/22
Aktuelle Erkrankungen
None
Vorgeschichte
HypoThyroidism since 1980 (regulated by medication), Heriditary high cholesterol (managed by medication)
Andere Medikamente
Synthroid, Atorvastatin,, off label Metformin use
Allergien
No Known allergies
Vorherige Impfungen
-

VAERS 2416330

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
17,0
Geschlecht
F
Eingang
19.08.2022
Impfdatum
09.01.2022
Beginn
09.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Antinuclear antibody increased Arthralgia COVID-19 Decreased appetite Dizziness Exposure to SARS-CoV-2 Fatigue Headache Laboratory test Malaise Myalgia Nausea SARS-CoV-2 antibody test negative

Symptomtext

Persistent symptoms (> 7 months) of fatigue, postexertional malaise, joint pain, myalgias, lightheadedness, headaches, nausea, and decreased appetite after receiving her COVID-19 booster. COVID-19 exposure around the same time but no documented COVID-19 infection and negative COVID-19 nucleocapsid antibodies. Patient recently had COVID-19 and has experienced worsening of symptoms.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
Lab results and work up in the intervening months have been otherwise normal, except for elevated ANA. However, she does not meet other criteria for a rheumatologic disease so this is being serially followed. She is being followed by multiple specialists for symptom management. Possible POTS diagnosis as well.
Aktuelle Erkrankungen
None
Vorgeschichte
Growth hormone deficiency, headaches, Duane syndrome of eye, pseudopapilledema, depressive disorder, ADHD
Andere Medikamente
Concerta, Wellbutrin
Allergien
none
Vorherige Impfungen
-

VAERS 2433349

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
-
Alter
48,0
Geschlecht
M
Eingang
21.07.2022
Impfdatum
19.01.2022
Beginn
29.01.2022
Tage bis Beginn
10,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Eczema Rash pruritic

Symptomtext

Narrative: HPI: 48y/o M, last seen 1 month ago for eczematous dermatitis thought 2/2 to COVID vaccination. Since that time, patient has been using triamcinolone ointment 1-2x daily as well as hydrocerin to good effect. He states that the rash is clearing significantly and he is no longer pruritic.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash pruritic
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2377316

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FJ5683

mild
Staat
VA
Alter
50,0
Geschlecht
F
Eingang
21.07.2022
Impfdatum
06.02.2022
Beginn
08.02.2022
Tage bis Beginn
2,0
Dosis
UNK
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Bruxism Dizziness Dysgeusia Hypoacusis Loss of personal independence in daily activities Pain in extremity Peripheral swelling Tinnitus Tooth fracture

Symptomtext

I received the pfizer covid 19 vaccine on 02/06/2022. At first I got a funny taste in my mouth from it I was a little light headed but that went away. On the 8th of February I woke up at 2:30 or so in the morning both my hands where swollen and hurting really bad I had to have my son cut my rings off cause no matter what I tried they would not slip over my knuckles. I had a high fregacery sound in my left ear. That has not gone away and can't hear to good out of it. I can not get any relief from it. I have never had a problem with my ears no infections in them even as a child. I reported this to my doctor who in turn told me it's because I'm getting older. I do not believe that I just turned 50 and never had anything wrong with my ears period. I know this is from the vaccine period. Now I don't know what to do I can not function with this high pitch fregacery in my ear. I have to get my teeth to get a little relief which in turn I have broke 2 teeth doing this. This is not fare. n

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
Have not had any
Aktuelle Erkrankungen
None
Vorgeschichte
Anxiety, depression, ptsd, neck and back pain sciatica. Adhd. High white cells and blood in urine.
Andere Medikamente
Tylenol 4 w/codeine Vyvanse Iburofen800mg
Allergien
-
Vorherige Impfungen
-

VAERS 2373992

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NY
Alter
67,0
Geschlecht
M
Eingang
19.07.2022
Impfdatum
18.04.2022
Beginn
14.07.2022
Tage bis Beginn
87,0
Dosis
4
Route/Site
SYR / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Cough Feeling abnormal Headache Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On July 14, 2022 I wasn't feeling and took an at home COVID-19 test and it was positive. I had a cough, headache, runny nose and low grade fever. I spoke to my doctor but we did not do anything, just waited it out. My symptoms lasted for 3 days.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
COVID- 19 test, positive, 7/14/22
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Lisinopril; Atorvastatin; Hydrochlorothiazide
Allergien
None
Vorherige Impfungen
-

VAERS 2373720

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
TN
Alter
52,0
Geschlecht
M
Eingang
19.07.2022
Impfdatum
15.04.2022
Beginn
15.07.2022
Tage bis Beginn
91,0
Dosis
4
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Cough Headache Lethargy Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

I had a sore throat, cough, lethargy, and a headache. I took an at-home COVID-19 test on 07/15/2022 that came back positive. I contacted my doctor and got a prescription for PAXLOVID and other steroid prescriptions. I began treatment the same day and started recovery the next day.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
COVID-19 test: 07/15/2022.
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
Omeprazole
Allergien
N/A
Vorherige Impfungen
-

VAERS 2370646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
GA
Alter
52,0
Geschlecht
F
Eingang
15.07.2022
Impfdatum
13.04.2022
Beginn
01.07.2022
Tage bis Beginn
79,0
Dosis
4
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Cough Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Approximately 3 months after my 4th dose vaccination I contracted COVID-19 and had the following symptoms: Cough, Sore Throat, Congestion. I called my Doctor and she prescribed me with an Antiviral medication for 5 days (4tabs/2x per day for 5 days). As of today 07/15/2022 I am feeling so much better now and all of my symptoms are gone.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Oropharyngeal pain
Hospital-Tage
-
Labordaten
COVID-19 Test
Aktuelle Erkrankungen
N/A
Vorgeschichte
High Blood Pressure; Asthma
Andere Medikamente
Lisinopril; Estrogen;
Allergien
Bactrim
Vorherige Impfungen
-

VAERS 2367452

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NY
Alter
71,0
Geschlecht
F
Eingang
13.07.2022
Impfdatum
12.04.2022
Beginn
23.06.2022
Tage bis Beginn
72,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Aphonia COVID-19 Cough Fatigue Feeling abnormal Pyrexia SARS-CoV-2 test positive

Symptomtext

06/23/2022 I was traveling and I started to lose my voice. 06/24/2022 I lost my voice completely 06/27/2022 I started to develop a cough, so I drank hot tea with honey, and it helped along with a hot shower. 06/28/2022 I wasn't feeling great, and I was actually supposed to catch a flight back home but my flight was canceled. 06/29/2022 I started taking the airborne, decongestion (which I only took it once it kept me from sleeping) and couch drops. I was feeling very fatigue. 06/30/2022 I got my flight home, and I took an at home COVID-19 Test and it came up negative. My voice is started to come back, and I still have the cough but only at night. 07/01/2022 I went to the COVID-19 Testing site and I was given another test and a PCR. The Rapid came back negative. I started having a low-grade fever. 07/02/2022 I received my PCR results and, they were positive. I called my PCP and she said it was too late to do the Paxlovid. The doctor also told me to keep doing my home remedies like airborne lots of fluid, tea and rest 07/08/2022 I would say I had recovered, and I was back to myself.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
COVID-19 at home PCR Rapid
Aktuelle Erkrankungen
NA
Vorgeschichte
Hip replaced Jan 2019 and Nov 2021
Andere Medikamente
Vitamin D 3
Allergien
NA
Vorherige Impfungen
-

VAERS 2367434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
PA
Alter
16,0
Geschlecht
M
Eingang
13.07.2022
Impfdatum
11.01.2022
Beginn
29.05.2022
Tage bis Beginn
138,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Fatigue Pyrexia SARS-CoV-2 test positive Sinus disorder

Symptomtext

On 05/29/22 he woke up a bit tired, but he had been in a parade the previous day in hot weather so I didn't think too much of it. He had a low grade fever that we treated with alternating Tylenol and Ibuprofen. I also gave him extra Vitamin C at that time. He was tested for COVID-19 on the third day at a local clinic and he was positive. By the time we received his PCR test results though his symptoms were improving to the point where medical intervention was not necessary. He only ran a fever for 2 days but was fatigued and had sinus like symptoms for around 4 days.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
COVID-19 PCR test- 06/01/2022-positive.
Aktuelle Erkrankungen
Unknown.
Vorgeschichte
Severe environmental allergies.
Andere Medikamente
Monthly Allergy Shot.
Allergien
None.
Vorherige Impfungen
-

VAERS 2366528

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NY
Alter
60,0
Geschlecht
M
Eingang
12.07.2022
Impfdatum
09.04.2022
Beginn
20.06.2022
Tage bis Beginn
72,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Cough Fatigue Infection Malaise Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Onset on June 20th (Day 1) I took a PCR and it was positive. I saw a doctor and got Paxlovid. Ended on day 7. Tested negative on 7,8 and 9. After day 10, I had a rebound and symptoms returned on day 13. Symptoms included congestion, cough and fatigue. With both infections, symptoms were the same. On day two with dose infections the symptoms were worse on day two and day three began to get better. I tested negative again on day 16 (July 5).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
Home PCR Health test, positive; negative; positive
Aktuelle Erkrankungen
N/A
Vorgeschichte
High Blood Pressure; Pre Diabetes
Andere Medikamente
Metformin; Amlodipine; Atenolol; Atorvastatin; Vitamin D3; Omega 3; Ocuvite
Allergien
Penicillin
Vorherige Impfungen
-

VAERS 2366335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NY
Alter
61,0
Geschlecht
F
Eingang
12.07.2022
Impfdatum
08.04.2022
Beginn
04.07.2022
Tage bis Beginn
87,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Disturbance in attention Fatigue Nasal congestion SARS-CoV-2 test SARS-CoV-2 test positive Somnolence

Symptomtext

Covid-19 infection positive home test 7/4/2022 stuffy nose, fatigue, sleepiness, trouble concentrating, 3-5 days duration for needing extra rest, Negative Home test 7/11/2022, mostly symptom-free. I was prescribed the Paxlovid and completed the 5 day course 7/8/2022.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
Positive antigen home test 7/4/2022 Negative test 7/11/2022 PCR test 7/12/2022 results pending
Aktuelle Erkrankungen
None
Vorgeschichte
Hay fever
Andere Medikamente
Muitivitamin, Vitamin D3, Calcium+Magnesium+D supplement
Allergien
Allergies to sulfa drugs, amoxycillin, erythromycin, macrodanton, cephalosporin
Vorherige Impfungen
-

VAERS 2362782

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NY
Alter
63,0
Geschlecht
F
Eingang
08.07.2022
Impfdatum
07.04.2022
Beginn
17.04.2022
Tage bis Beginn
10,0
Dosis
4
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Pyrexia SARS-CoV-2 test positive Sneezing Vaccine breakthrough infection

Symptomtext

Breakthrough Case, two weeks after dose 4 of vaccine. Started off with a fever and constantly sneezing. Took a few home tests and they came back negative, after 4 days finally tested positive on 4/19/2022. I called my Dr's office, and we decided not to take any medications, and just wait it out.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
NA
Vorgeschichte
Arthritis
Andere Medikamente
Meloxicam; A Reds 2; Pepsid; Calcium D3 supplements; Acetaminophen; Claritin
Allergien
Doxycycline; Iodine Dermatitis; Skin allergies; Hayfever
Vorherige Impfungen
-

VAERS 2359799

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
VA
Alter
71,0
Geschlecht
M
Eingang
06.07.2022
Impfdatum
04.04.2022
Beginn
24.06.2022
Tage bis Beginn
81,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Headache Illness Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

I contracted COVID-19 on 06/24/2022 with symptoms of irritated throat, and mild headache. I was prescribed Paxlovid on 06/25/2022. My symptoms initially resolved on 06/25/20022. On Day 7 of my illness a slight headache returned and I developed a runny nose. I am still experiencing a slightly runny nose, and slight headache but they are not as prominent.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
COVID-19 rapid nasal antigen home test was positive on 06/25/2022
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
Omasartan; Fish Oil; Multivitamin
Allergien
N/A
Vorherige Impfungen
-

VAERS 2345372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
OR
Alter
53,0
Geschlecht
M
Eingang
30.06.2022
Impfdatum
10.01.2022
Beginn
12.01.2022
Tage bis Beginn
2,0
Dosis
UNK
Route/Site
SYR / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Anxiety Fatigue Hypersensitivity

Symptomtext

Fatigue, Anxiety, New Allergies

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Hydrochlorothiazide, Potassium Chloride
Allergien
Penicillin
Vorherige Impfungen
-

VAERS 2326658

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
FL
Alter
62,0
Geschlecht
F
Eingang
22.06.2022
Impfdatum
16.06.2022
Beginn
17.06.2022
Tage bis Beginn
1,0
Dosis
4
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Rash macular

Symptomtext

on her arms and thighs she noticed some red splotches that don't itch; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 62-year-old female patient received BNT162b2 (BNT162B2), on 16Jun2022 as dose 4 (booster), single (Lot number: FJ5683) at the age of 62 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "hyperactive thyroid" (ongoing), notes: diagnosed with hyperactive thyroid at age 24; "Sjogren's disease" (ongoing), notes: Sjogrens disease and symptoms started approximately 20 years ago.; "seasonal allergies" (unspecified if ongoing). Concomitant medication(s) included: ASTELIN [AZELASTINE HYDROCHLORIDE] nasal taken for seasonal allergy, start date: 10Jun2022; MONTELUKAST SODIUM oral taken for seasonal allergy, start date: 10Jun2022. Vaccination history included: BNT162b2 (Dose 1, Lot No: EL9263), administration date: 26Feb2021, when the patient was 61-year-old, for Covid-19 Immunization; BNT162b2 (Dose 2, Lot No: EN6198), administration date: 19Mar2021, when the patient was 61-year-old, for Covid-19 Immunization; BNT162b2 (Dose 3 (1st booster), Lot No: FC3184.), administration date: 01Oct2021, when the patient was 61-year-old, for Covid-19 Immunization, reaction(s): "has ringworm that began on 10Jun2022". The following information was reported: RASH MACULAR (non-serious) with onset 17Jun2022, outcome "unknown", described as "on her arms and thighs she noticed some red splotches that don't itch". Additional Information: Stated she got her second booster for the Pfizer covid vaccine yesterday (16Jun2022) administered on right upper arm and just finished her workday and looked down and her arms have gotten all splotchy and it was not really like a rash but for a very pale skinned person she has little red splotches all up and down her arms and has it on her thighs down over her knees and the skin was all red with splotches and she was calling to know if she should freak out about this or it will go away the same as the redness around the site after the vaccines. Stated the red splotches just were noticed right before she started looking for a phone number to call. Stated for the red spotches she has not started anything or taken anything for this. Stated she also has ringworm that began and she started taking an antifungal cream last Friday and that was when she noticed it and had the HCP through telehealth when she was asking about her allergies she gave the caller a topical treatment to use for that but only on her legs and not on her arms and the ringworm began on 10Jun2022; states it is distressing that she cannot find the antifungal cream and needs to find it before the end of the day. Patient stated the topical antifungal cream is Ketoconazole to apply topically daily to affected areas for two weeks and to keep it on as often as possible; stated the Ketoconazole has lot 637121, expiry date Jan2024 and has GTIN and SN number and also has NDC 00093-3219-92; states the Ketoconazole was to be put on the two spots of ringworm she has and was still getting ringworm and is taking Ketoconazole still and this morning she had a second location where it was starting and started using the antifungal cream for that. Astelin started a week ago states she had really bad outbreak of allergic seasonal allergies but it was not infection- 1 percent nasal solution two sprays twice per day and reduced this week to one spray twice a day. Comments: Sjogrens disease and symptoms started approximately 20 years ago; states she does not know if Pfizer records any other kind of health issues but the Sjogrens and the hypoactive thyroid are her two autoimmune diseases and sometimes other health issues play into a reaction.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash macular
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Hyperthyroidism (diagnosed with hyperactive thyroid at age 24); Sjogren's disease (Sjogrens disease and symptoms started approximately 20 years ago.)
Vorgeschichte
Medical History/Concurrent Conditions: Seasonal allergy
Andere Medikamente
ASTELIN [AZELASTINE HYDROCHLORIDE]; MONTELUKAST SODIUM
Allergien
-
Vorherige Impfungen
-

VAERS 2313794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
-
Alter
45,0
Geschlecht
M
Eingang
09.06.2022
Impfdatum
02.06.2022
Beginn
02.06.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Body temperature Pain in extremity Pyrexia

Symptomtext

This is a spontaneous report received from a non-contactable reporter (consumer or other non-HCP). The reporter is the patient. A 45-year-old male patient received bnt162b2 (BNT162B2) on 02Jun2022 as dose 3 (booster), single (Lot number: FJ5683), in left arm, for COVID-19 immunization. The patient's relevant medical history was not reported. The patient did not receive any concomitant medications. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: EL3247; Anatomical site: Left arm), administration date: 04Mar2021, when the patient was 44 years old, for COVID-19 immunization and Bnt162b2 (DOSE 2, SINGLE; Lot number: HEP6955; Anatomical site: Left arm), administration date: 25Mar2021, when the patient was 44 years old, for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 02Jun2022, outcome "not recovered", described as "Fever 102.5"; PAIN IN EXTREMITY (non-serious) with onset 02Jun2022, outcome "not recovered", described as "Left arm pain". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of pyrexia and pain in extremity. Additional information: Prior to the vaccination, the patient was not diagnosed with COVID-19. The patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. Treatment included ADVIL and TYLENOL for PYREXIA and PAIN IN EXTREMITY. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
Test Date: 20220602; Test Name: Body temperature; Result Unstructured Data: Test Result:102.5 (unspecified units); Comments: Fever 102.5.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2292897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
PR
Alter
14,0
Geschlecht
F
Eingang
24.05.2022
Impfdatum
12.01.2022
Beginn
13.01.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Dizziness Hyperhidrosis Pallor Vomiting

Symptomtext

Patient of 14 years of age, one day after her third booster of the dose of PFIZER 0.3ml, the same, Around 7:00am, she presented, vomit, paleness, dizziness and sweating. The parents called the 911 service and she was transported to the hospital where she was hydrated.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
No
Aktuelle Erkrankungen
NO
Vorgeschichte
NO
Andere Medikamente
No
Allergien
NO
Vorherige Impfungen
-

VAERS 2284594

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NY
Alter
71,0
Geschlecht
M
Eingang
19.05.2022
Impfdatum
11.04.2022
Beginn
14.04.2022
Tage bis Beginn
3,0
Dosis
4
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Arterial disorder Blood pressure increased Blood pressure measurement Cluster headache Computerised tomogram head Ear discomfort Giant cell arteritis Hyperaesthesia Necrosis of artery Red blood cell sedimentation rate Sudden hearing loss

Symptomtext

He developed a small area of necrosis on the left temporal artery; and it felt like he could not hear; Caller states his temporal arteries were engorged, sensitive to touch; His blood pressure elevated to 170/95; He had the sensation of gauze or cotton in his ear; concerned he may be developing temporal arteritis; He woke up with a splitting headache; his temporal arteries were engorged, sensitive to touch; This is a spontaneous report received from contactable reporter(s) (Physician). The reporter is the patient. A 71-year-old male patient received BNT162b2 (BNT162B2), on 11Apr2022 as dose 4 (booster), single (Lot number: FJ5683) at the age of 71 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Immunocompromised", start date: 1990 (ongoing), notes: Exposed to blood from a patient with HIV, and he turned positive for HIV, since the 1990s.; "Coronary artery disease", start date: 1990 (ongoing), notes: He had a history of coronary artery disease, and has 4 stents in his heart.; "Hyperlipidemia", start date: 1990 (ongoing); "Exposed to blood from a patient with HIV", start date: 1990 (unspecified if ongoing), notes: he turned positive for HIV, since the 1990s. Diagnosed HIV, but was currently undetectable.; "Caller states he has a history of coronary artery disease, and has 4 stents in his heart." (unspecified if ongoing). There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 1, single, Lot Number/Expiry Date: EN6202/unknown, Anatomical Location: left arm), administration date: 28Feb2021, when the patient was 69-year-old, for Covid-19 Immunization, reaction(s): "No"; BNT162b2 (Dose 2, single, Lot Number/ Expiry Date: Caller states as an E or L N6206, probably an E. Route, Anatomical Location: left arm), administration date: 21Mar2021, when the patient was 70-year-old, for Covid-19 Immunization, reaction(s): "No"; BNT162b2 (Dose 3 (Booster), single, Lot Number/Expiry Date: EW0173/unknown, Route, Anatomical Location: left arm), administration date: 31Aug2021, when the patient was 70-year-old, for Covid-19 Immunization, reaction(s): "No". The following information was reported: ARTERIAL DISORDER (medically significant) with onset 14Apr2022, outcome "not recovered", described as "Caller states his temporal arteries were engorged, sensitive to touch"; EAR DISCOMFORT (medically significant) with onset 14Apr2022, outcome "recovering", described as "He had the sensation of gauze or cotton in his ear"; CLUSTER HEADACHE (medically significant) with onset 14Apr2022, outcome "recovering", described as "He woke up with a splitting headache"; BLOOD PRESSURE INCREASED (medically significant) with onset 14Apr2022, outcome "recovering", described as "His blood pressure elevated to 170/95"; SUDDEN HEARING LOSS (medically significant) with onset 14Apr2022, outcome "recovering", described as "and it felt like he could not hear"; GIANT CELL ARTERITIS (medically significant) with onset 14Apr2022, outcome "not recovered", described as "concerned he may be developing temporal arteritis"; HYPERAESTHESIA (medically significant) with onset 14Apr2022, outcome "not recovered", described as "his temporal arteries were engorged, sensitive to touch"; NECROSIS OF ARTERY (medically significant) with onset 18Apr2022, outcome "not recovered", described as "He developed a small area of necrosis on the left temporal artery". The events "he developed a small area of necrosis on the left temporal artery", "and it felt like he could not hear", "caller states his temporal arteries were engorged, sensitive to touch", "his blood pressure elevated to 170/95", "he had the sensation of gauze or cotton in his ear", "concerned he may be developing temporal arteritis", "he woke up with a splitting headache" and "his temporal arteries were engorged, sensitive to touch" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Blood pressure measurement: (unspecified date) 140/80, notes: his normal blood pressure; (14Apr2022) 170/95; Computerised tomogram head: (unspecified date) small area of necrosis on the left temporal artery; Red blood cell sedimentation rate: (unspecified date) normal. Clinical information: No Prior Vaccinations (within 4 weeks). Vaccine was not administered at Facility. Caller stated that he was a physician, and specified as paediatric psychiatrist. He took the fourth dose of the Pfizer Covid 19 vaccine. About 3 days, after his fourth dose of vaccine, he woke up with a splitting headache and his temporal arteries were engorged and they were sensitive to touch. He still had a headache but it was no longer a splitting headache. He had the sensation of gauze or cotton in his ear and it felt like he could not hear. Caller states it was not as pronounced as it was. His normal blood pressure was about 140/80 and his blood pressure elevated to 170/95. He decided to wait and see if the effects were transitory, but he was concerned he might be developing temporal arteritis. He went to the emergency room but was not admitted, just to get a SED rate, and a brain scan. The SED rate was normal, but his brain CT, had the recommendation to get a biopsy of the left temporal artery and would prefer him to have a neurological consult, because he developed a small area of necrosis on the left temporal artery. He went to the ED because he noticed a necrotic area on his temporal artery. He agreed to complete a report. Seriousness: Caller first states as serious, then later, documents as medically significant, because it could lead to other things.; Sender's Comments: Based on the available information, there is a reasonable possibility of a causal relationship between the suspect vaccine BNT162B2 (COMIRNATY) and reported events which cannot be fully assessed/excluded. The case will be reassessed if additional information becomes available. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cluster headache
Hospital-Tage
-
Labordaten
Test Name: blood pressure; Result Unstructured Data: Test Result:140/80; Comments: his normal blood pressure; Test Date: 20220414; Test Name: blood pressure; Result Unstructured Data: Test Result:170/95; Test Name: brain scan; Result Unstructured Data: Test Result:small area of necrosis on the left temporal artery; Test Name: SED rate; Result Unstructured Data: Test Result:normal
Aktuelle Erkrankungen
Coronary artery disease (He had a history of coronary artery disease, and has 4 stents in his heart.); Hyperlipidemia; Immunocompromised (Exposed to blood from a patient with HIV, and he turned positive for HIV, since the 1990s.)
Vorgeschichte
Medical History/Concurrent Conditions: HIV test positive (he turned positive for HIV, since the 1990s. Diagnosed HIV, but was currently undetectable.); Stent placement
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2280919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
GA
Alter
64,0
Geschlecht
M
Eingang
17.05.2022
Impfdatum
30.03.2022
Beginn
31.03.2022
Tage bis Beginn
1,0
Dosis
4
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Chills Fatigue Flank pain Neck pain Pain Pain in extremity Pyrexia

Symptomtext

I had soreness in the left side that radiated to the next and shoulder. To the other side of my right arm and right shoulder. I felt symptoms of possible flu. Fatigue was intense, the chills, the fever. And it lasted about 3 weeks. Previous injections did not give me that reaction. Doctor put me on ibuprofen 6mg, cyclobenzaprine 5mg for 10 days, methylprednisolone 4mg for 6 days. I from time to time still get pain randomly on my thumbs, however my doctor does not believe that is a reaction to the vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Lung holler
Andere Medikamente
Synthroid 0.75mg; amlodipine besylate; metoprolol citrate; cetirizine 10mg; omeprazole 40mg; Tadalafil 5mg; famotidine 40mg; magnesium 40mg; zinc 50mg; 2 turmeric 1000mg each; 3 chewable elderberries; D3 1 gummies; B12 5000MG; ashwagandha 1
Allergien
Sulfites; latex sensitivity
Vorherige Impfungen
-

VAERS 2278173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
RI
Alter
51,0
Geschlecht
M
Eingang
16.05.2022
Impfdatum
18.01.2022
Beginn
02.05.2022
Tage bis Beginn
104,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Cough Fatigue Oropharyngeal pain Pain SARS-CoV-2 test positive

Symptomtext

I had a sore throat and cough when I woke up in the morning. I felt really fatigue and had body aches. I took cough suppressants and my daily medications to help reduce my cough. I went to the clinic to get tested on 05/02/2022, and it came back positive for COVID-19. I quarantined for 10 days and have felt better since then and just returned back to work on 05/16/2022 after my PCR test came back negative on 05/12/2022.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
COVID-19 tests: 05/02/2022 & 05/12/2022
Aktuelle Erkrankungen
N/A
Vorgeschichte
Diabetes, High Blood Pressure
Andere Medikamente
Metformin, Ozempic, Lisinopril, Hydro, Amlodipine, Amiloride, Aspirin
Allergien
N/A
Vorherige Impfungen
-

VAERS 2264972

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

mild
Staat
NY
Alter
64,0
Geschlecht
F
Eingang
05.05.2022
Impfdatum
05.05.2022
Beginn
05.05.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest discomfort Dizziness

Symptomtext

Fifteen minutes post Pfizer vaccine booster administration patient reported feeling light headed, dizzy, and pressure/heaviness in chest. EMS was called and patient was transferred via chair to ambulance by EMS.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
unknown
Vorgeschichte
unknown
Andere Medikamente
unknown
Allergien
unknown
Vorherige Impfungen
-

VAERS 2260141

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
SC
Alter
72,0
Geschlecht
F
Eingang
02.05.2022
Impfdatum
27.04.2022
Beginn
29.04.2022
Tage bis Beginn
2,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Fatigue Headache Myalgia Sneezing

Symptomtext

Sneezing, fatigue, headache, muscle and joint pain

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
edarbycor, toprol, amlodipine
Allergien
none
Vorherige Impfungen
-

VAERS 2256478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
MA
Alter
-
Geschlecht
F
Eingang
28.04.2022
Impfdatum
15.02.2022
Beginn
06.05.2021
Tage bis Beginn
-
Dosis
3
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Physiotherapy Product administered at inappropriate site Ultrasound scan Vaccination site pain

Symptomtext

Dull aches to the left site of the injection site (side of thigh); Anatomical Site of injection- Left quadricep; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old female patient received BNT162b2 (BNT162B2), on 06May2021 as dose 2, single (Lot number: EW0179) and on 15Feb2022 as dose 3 (booster), single (Lot number: FJ5683), all intramuscular for covid-19 immunisation. The patient's relevant medical history included: "Hormone replacement" (unspecified if ongoing); "Sleep aid" (unspecified if ongoing). Concomitant medication(s) included: ESTROGENS CONJUGATED; METHYLTESTOSTERONE oral taken for hormone replacement therapy (ongoing); PROGESTERONE taken for hormone replacement therapy (ongoing); TRAZODONE taken for sleep disorder (ongoing); CALCIUM (ongoing). Vaccination history included: BNT162b2 (Dose 1, single; Batch/ Lot number- ER8733; via Intramuscular route in Left deltoid), administration date: 27Mar2021, when the patient was 60-year-old, for COVID-19 Immunization, reaction(s): "Dull ache", "Her arm never stopped hurting/continuous arm ache", "burning sensation". The following information was reported: PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (non-serious) with onset 06May2021, outcome "unknown", described as "Anatomical Site of injection- Left quadricep"; VACCINATION SITE PAIN (non-serious) with onset 06May2021, outcome "recovering", described as "Dull aches to the left site of the injection site (side of thigh)". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Anatomical site of injection was Left quadricep for dose 2 and dose 3. Patient was taking multivitamin tablets; Progesterone 100 mg and Trazodone 50 mg at present. Relevant tests included Ultrasound with negative results in Apr2021 and Physical therapy assessment with negative results in Apr2021 and with comments as no loss of stomach or range of motion or flexibility noted. Patient received the 2nd and 3rd dose in my left quadriceps, also have dull aches to the left site of the injection site (side of thigh). The pain has subsided somewhat over time, but it has never completely gone away.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Vaccination site pain
Hospital-Tage
-
Labordaten
Test Date: 202104; Test Name: Physical therapy assessment; Test Result: Negative ; Comments: No loss of stomach or range of motion or flexibility noted.; Test Date: 202104; Test Name: Ultrasound; Test Result: Negative
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Hormone replacement therapy; Sleep disorder
Andere Medikamente
ESTROGENS CONJUGATED;METHYLTESTOSTERONE; PROGESTERONE; TRAZODONE; CALCIUM
Allergien
-
Vorherige Impfungen
-

VAERS 2241054

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NY
Alter
67,0
Geschlecht
F
Eingang
19.04.2022
Impfdatum
31.03.2022
Beginn
01.04.2022
Tage bis Beginn
1,0
Dosis
4
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Blood test Computerised tomogram normal Extra dose administered Headache Pain

Symptomtext

Approximately 2 weeks after my 2nd booster (4th dose vaccination) I experienced the following symptoms: Headache (Constant headache). I took Tylenol (Extra strength), Tylenol Dual, it would lessen the pain but it did not do anything to make the headache go away. I saw my primary care who advised me to get a CT Scan and the result was normal. I was given an IV medication of electrolyte, and prescribed with Toradol and Reglan. As of today 04/19/2022 my headache isn't as severe and the pain is tolerable.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
CT Scan. Blood work.
Aktuelle Erkrankungen
COPD; Asthma
Vorgeschichte
COPD; Asthma; Constipation
Andere Medikamente
Omeprazole; Breztri; Montelukast; Theophylline; Albuterol Inhaler; Atorvastatin; Ramipril; Amlodipine; Centrum; Vitamin C; Biotin; Iron; Garlic Tablets; Nicotine Patch
Allergien
Penicillin; Amoxicillin
Vorherige Impfungen
-

VAERS 2238167

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
TX
Alter
11,0
Geschlecht
F
Eingang
17.04.2022
Impfdatum
20.01.2022
Beginn
20.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered Pain Product administered to patient of inappropriate age

Symptomtext

It was discovered on 04/14/2022, the Patient mistakenly received Pfizer COVID vaccine for age 12 and older at age 11yrs 9months on 01/20/2022. This was the first dose in the series. Patient was watched for standard 15 minutes after receiving Pfizer COVID vaccine and Influenza vaccine without any signs adverse reaction. Mother of patient was notified on 04/14/2022, and informed us the Patient only experienced soreness the next day after receiving vaccines.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
-
Allergien
No known medication allergies
Vorherige Impfungen
-

VAERS 2237619

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
OH
Alter
76,0
Geschlecht
M
Eingang
16.04.2022
Impfdatum
18.03.2022
Beginn
18.03.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Fatigue Pain Poor quality product administered Product administration error

Symptomtext

A dose of the vaccine was given to the patient after being stored at room temperature in a syringe for more than 12hrs. Additional to the allowable 12hrs, vaccine was left for an additional 16hrs.; A dose of the vaccine was given to the patient after being stored at room temperature in a syringe for more than 12hrs. Additional to the allowable 12hrs, vaccine was left for an additional 16hrs.; very tired; body aches; This is a spontaneous report received from contactable reporter(s) (Pharmacist) from medical information team. A 76-year-old male patient received BNT162b2 (COMIRNATY), on 18Mar2022 at 13:30 as dose 2, 30 ug single (Lot number: FJ5683) at the age of 76 years intramuscular, in left deltoid for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: METOPROLOL TARTRATE ACCORD oral taken for heart rate decreased, start date: 16Dec2021 (ongoing); FERROUS SULFATE oral taken for mineral supplementation, start date: 29Dec2021 (ongoing). Vaccination history included: comirnaty (as dose 1, single, Time: 13.31, Anatomical Site of injection: Left Deltoid, Route of administration: Intramuscular, Batch/Lot number: FJ5683), administration date: 25Feb2021, for COVID-19 immunisation. The following information was reported: POOR QUALITY PRODUCT ADMINISTERED (non-serious), PRODUCT ADMINISTRATION ERROR (non-serious) all with onset 18Mar2022 at 13:30, outcome "unknown" and all described as "A dose of the vaccine was given to the patient after being stored at room temperature in a syringe for more than 12hrs. Additional to the allowable 12hrs, vaccine was left for an additional 16hrs."; PAIN (non-serious) with onset 2022, outcome "unknown", described as "body aches"; FATIGUE (non-serious) with onset 2022, outcome "unknown", described as "very tired". Additional information: The pharmacist wanted to report an administration error for Pfizer-BioNTech COVID-19 vaccine (gray cap). Reporter stated that a dose of the vaccine was given to the patient after being stored at room temperature in a syringe for more than 12 hours. Additional to the allowable 12 hours of storage, they left the vaccine for an additional 16 hours. The pharmacist then asked for stability information on the vaccine, what to do if they have to repeat a dose, and revaccination guidelines after having a patient receive the second dose 16 hours after the use-by-date. The reporter assessed the events as serious, medically significant and reported the relatedness of the drug to the events as unrelated. The pharmacist felt it was significant as it was past its expiration time. Stated they mistakenly kept it in the "fridge" (as reported) longer than they should have. Upon follow-up 12Apr2022 it was reported that the patient did not provided information regarding the reported adverse event(s) with the use of the product. Vaccination Facility Type: Public health clinic / Facility. No Prior Vaccinations (within 4 weeks). No relevant tests. The type of Medication error was patient received correct drug and dosage but covid vaccine was out of date range in refrigerator by 28 and ? hours. Stability is the issue here. The type of error is the preparation of the covid 19 vaccine , as stated above vaccine was drawn up in syringe kept in the refrigerator but the date was expired for the vaccine. Again, it is all about stability of the product that was given to the patient, it was 28and ? hours. The medication error happened because the syringe with vaccine in it was not removed at the end of day nor removed first thing in the morning and destroyed. Since this happened we have change our process and the person who fills out the covid tracker daily now destroyed the unused Vaccine at night. The patient was not affected physically. The patient did received an unstable vaccine but when I spoke to patient he said he got very tried and body ache for 2days after covid injection. patient was taking that as good news as the injection of covid 19 was doing its job. At this time his Provider does not want to give him a second shot of vaccine due to patient had signs that the vaccine worked. We have decided to just let him received his booster shot when due and patient is fine with his. No clinical consequence on the patients part. The lot number for BNT162B2 was not provided and will be requested during follow up. Follow-up (12Apr2022): This is a spontaneous follow-up report received from a contactable Pharmacist This Pharmacist reported for a 76-year-old male patient. Updated information included: New reporter information in slider#02, patient information (AGE), (Vaccination information in chart), new event, concomitants drug. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
Andere Medikamente
METOPROLOL TARTRATE ACCORD; FERROUS SULFATE
Allergien
-
Vorherige Impfungen
-

VAERS 2155115

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
PA
Alter
72,0
Geschlecht
F
Eingang
08.04.2022
Impfdatum
03.03.2022
Beginn
03.03.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Nausea

Symptomtext

Patient presents for covid vaccination. Vaccination administered, and patient was observed after 15 minutes for reaction. After the 9 minutes patient reported feeling lightheaded and nauseous. Patient's BP was 118/60, pulse 76, PA-C evaluated patient. Patient drank some water and is feeling better. Patient monitored for a full 25 minutes in the office after the vaccine was given. Patient reports she is feeling OK now- 3:06 PM. Walked patient out to the lobby- patient again felt lightheaded. Patient sat and got another drink of water. evaluated patient. Patient sat for another couple minutes and left at 3:19pm.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2213611

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
-
Alter
52,0
Geschlecht
M
Eingang
03.04.2022
Impfdatum
21.03.2022
Beginn
21.03.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain in extremity

Symptomtext

LEFT ARM SORENESS

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2196492

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

mild
Staat
NC
Alter
22,0
Geschlecht
F
Eingang
24.03.2022
Impfdatum
24.03.2022
Beginn
24.03.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Dizziness Vision blurred

Symptomtext

Customer felt dizzy with blurred vision after administration of COVID-19 shot. She was given some water, helped to a sitting position on the floor and Paramedics called. After about one hour she informed Paramedics that she was fine. Customer was advised to call with any other symptoms.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2185939

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
68,0
Geschlecht
M
Eingang
17.03.2022
Impfdatum
11.03.2022
Beginn
12.03.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Vertigo

Symptomtext

Woke up Saturday morning with extreme dizziness, Vertigo

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2184363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
67,0
Geschlecht
F
Eingang
17.03.2022
Impfdatum
15.03.2022
Beginn
15.03.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Injection site erythema Injection site pain Injection site reaction Injection site swelling Local reaction

Symptomtext

local injection site reaction. red circle bump around injection area. painful for patient lasting minimum 2 days after she received shot. red area getting a little bigger and not clearing up.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2181975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
35,0
Geschlecht
F
Eingang
16.03.2022
Impfdatum
04.02.2022
Beginn
04.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Depression Hypersensitivity Pruritus Rash Skin injury Skin reaction Urticaria

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient.A 35 year-old female patient received bnt162b2 (BNT162B2), administered in arm left, administration date 04Feb2022 09:00 (Lot number: FJ5683) at the age of 35 years as dose 3 (booster), single for covid-19 immunisation. The patient had no relevant medical history. The patient took concomitant medications. Vaccination history included: Bnt162b2 (Dose: 1st, Time: AM, Anatomical Site of injection: Left arm, Batch/Lot Number: EW0177), administration date: 21May2021, when the patient was 34 years old, for Covid-19 immunization; Bnt162b2 (Dose: 2nd, Time: PM, Anatomical Site of injection: Left arm, Batch/Lot Number: EW0181), administration date: 11Jun2021, when the patient was 34 years old, for Covid-19 immunization. The following information was reported: DEPRESSION (non-serious), outcome "unknown", described as "Depression"; SKIN INJURY (non-serious), outcome "unknown", described as "my skin got badly damage"; SKIN REACTION (non-serious) with onset 04Feb2022 21:00, outcome "not recovered", described as "Skin reaction"; RASH (non-serious) with onset 04Feb2022 21:00, outcome "recovered with sequelae", described as "still have the same rash and big; getting worse; got it all over the body, whole body"; PRURITUS (non-serious) with onset 04Feb2022 21:00, outcome "not recovered", described as "Itchy"; HYPERSENSITIVITY (non-serious), outcome "unknown", described as "allergic reaction"; URTICARIA (non-serious), outcome "unknown", described as "hives". The event "depression" was evaluated at the physician office visit. The events "my skin got badly damage", "skin reaction", "still have the same rash and big; getting worse; got it all over the body, whole body", "itchy", "allergic reaction" and "hives" were evaluated at the physician office visit and emergency room visit. Therapeutic measures were taken as a result of skin injury, skin reaction, rash, pruritus, hypersensitivity, urticaria. Additional information: The patient got a rash for more than 7 days; it was already 11 days after the vaccine it was still the same rash and big. The patient kept putting, and already got like bottles of Hydrocortisone (1GT0334) already all over and it had been a long time. The rash was only getting worse. The patient had been trying to keep it under control with cortisone. The patient got the shot in the morning 9:00 and then like by 21:00 that was when the patient started feeling the rash and itchy and then she was putting creams and steroids and all the stuff she took a Benadryl (S211181), and Hydrocortisone for a week but was not getting better. The patient's whole body was affected (arms, back, side, chest, neck, arms, right side). Prior vaccination (4 weeks prior) she took the last one like in Jun and the another one before that was Dec (Further clarification unknown). She had ugly itchy rashes all over her body, tired all the over the counter medicine none worked, had antibiotic tried different antihistamine like Benadryl, Claritin, equate nothing helped. Suffered 2 weeks and decided to see a doctor to get different findings and opinions. It was confirmed that she was allergic to booster that gave her hives and bad skin so she was prescribed by steroid injection and medication for another one week so far it helped clear her skin a little but still had patches in her body. After 2 week she went to see 2 doctors because she was suffering for 2 weeks of depression due to her skin that got badly damage with rashes and hives, no medicine worked, first doctor told her that she had an allergic reaction from a booster so she advised me to get a steroid shot and get a IV to help with my recovery and second I went to urgent care and got a shot of steroid and given a prednisone for a week and the rash got cleared up a little but still recovering few patches in my skin due to allergies/hives from a booster shot.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History:Patient Other Relevant History 1: None, Comment: Patient History: No.
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2181886

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
PA
Alter
12,0
Geschlecht
F
Eingang
16.03.2022
Impfdatum
10.01.2022
Beginn
10.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
OT / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Fatigue Pain Pain in extremity Pyrexia

Symptomtext

sore arm; Fever; Exhausted; Achy; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 12 year-old female patient (not pregnant) received bnt162b2 (BNT162B2), intramuscular, administered in arm left, administration date 10Jan2022 (Lot number: FJ5683) at the age of 12 years as dose 3 (booster), single for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Bnt162b2 (Dose Number: 2, Batch/Lot No: EW0185, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 02Jun2021, when the patient was 11 years old, for Covid-19 immunization; Bnt162b2 (Dose Number: 1, Batch/Lot No: EN5318, Location of injection: Arm Left, Route of Administration: Intramuscular), administration date: 12May2021, when the patient was 11 years old, for Covid-19 immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 10Jan2022, outcome "recovered" (11Jan2022), described as "sore arm"; PYREXIA (non-serious) with onset 10Jan2022, outcome "recovered" (11Jan2022), described as "Fever"; FATIGUE (non-serious) with onset 10Jan2022, outcome "recovered" (11Jan2022), described as "Exhausted"; PAIN (non-serious) with onset 10Jan2022, outcome "recovered" (11Jan2022), described as "Achy". Therapeutic measures were not taken as a result of pain in extremity, pyrexia, fatigue, pain. Additional information: Prior to the vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive any other vaccines within four weeks prior to the vaccination. Facility type vaccine was Public Health Clinic/Administration facility. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2177362

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
56,0
Geschlecht
M
Eingang
13.03.2022
Impfdatum
09.02.2022
Beginn
13.03.2022
Tage bis Beginn
32,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Arthralgia Pain

Symptomtext

Patient called this afternoon claiming his left shoulder is sore from the Pfizer COVID vaccine he received on February 9, 2022. He states his left shoulder has been sore for over a month and has not gotten better. It hurts when he moves his arm but is okay if he does not move the arm. Patient had used IBU and had iced the sore shoulder. Patient was advised to see a medical doctor to look at the area but he claims he does not have insurance to pay for the visit. Patient was advised to continue is current regimen of IBU and icing the shoulder.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
unknown
Vorgeschichte
unknown
Andere Medikamente
patient stated he's been taking IBU and icing the sore area
Allergien
NKA
Vorherige Impfungen
-

VAERS 2191862

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
-
Alter
39,0
Geschlecht
F
Eingang
10.03.2022
Impfdatum
08.02.2022
Beginn
08.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chills Fatigue Headache Pain

Symptomtext

Headache BODY ACHES, CHILLS, FATIGUE Narrative:

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2191857

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
-
Alter
51,0
Geschlecht
F
Eingang
10.03.2022
Impfdatum
02.02.2022
Beginn
02.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Headache Pain in extremity Peripheral swelling

Symptomtext

Headache ARM PAIN AND SWELLING Narrative:

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2161931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
PA
Alter
36,0
Geschlecht
F
Eingang
05.03.2022
Impfdatum
03.03.2022
Beginn
04.03.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Lymphadenopathy Rash

Symptomtext

pt had lymph node swelling in armpit upper breast 12 hours post vaccine, rash development 24hrs post in same location of lymp node swelling and under arm

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
DM1 allergies
Andere Medikamente
insulin birth control trazdone Effexor zyrtec
Allergien
PCN shell fish
Vorherige Impfungen
-

VAERS 2147527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
IN
Alter
34,0
Geschlecht
M
Eingang
27.02.2022
Impfdatum
25.02.2022
Beginn
26.02.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Pain Pyrexia

Symptomtext

Fever of 102 within 12 hours of vaccine. Moderate to severe body aches and dizziness. Symptoms lasted 48 hours. No treatment applied. Full recovery.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
None.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2140681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
15,0
Geschlecht
F
Eingang
25.02.2022
Impfdatum
22.02.2022
Beginn
23.02.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site erythema Injection site pruritus Injection site swelling

Symptomtext

Redness, swelling and itching at injection site.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2139842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NJ
Alter
29,0
Geschlecht
F
Eingang
25.02.2022
Impfdatum
16.01.2022
Beginn
19.01.2022
Tage bis Beginn
3,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Neck pain Pain

Symptomtext

neck pain radiating down to bilateral shoulders

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2131318

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NY
Alter
54,0
Geschlecht
M
Eingang
22.02.2022
Impfdatum
14.02.2022
Beginn
15.02.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Dysgeusia Fatigue

Symptomtext

Patient reporting experiencing metallic taste mouth , unusual tiredness and feeling faint upon standing starting day after receiving vaccines to present day

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
unknown
Vorgeschichte
unknown
Andere Medikamente
unknown
Allergien
unknown
Vorherige Impfungen
-

VAERS 2128296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
WA
Alter
43,0
Geschlecht
F
Eingang
19.02.2022
Impfdatum
19.02.2022
Beginn
19.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Nausea Vomiting

Symptomtext

Patient experienced lightheaded, nausea, and vomiting about 5-10 minutes after vaccination. Patient sat down and for observation. Paramedics were called to take blood pressure and monitor the patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Unknown
Vorgeschichte
Anxiety Pinched Nerve
Andere Medikamente
Sertraline Gabapentin
Allergien
None
Vorherige Impfungen
-

VAERS 2128164

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NY
Alter
24,0
Geschlecht
F
Eingang
19.02.2022
Impfdatum
26.01.2022
Beginn
26.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Abdominal pain Blood test Computerised tomogram Illness Lymphadenopathy Nasopharyngitis Nausea Sleep disorder Ultrasound scan Urine analysis

Symptomtext

I started to feel nauseous out of no where; I started to feel nauseous out of no where, I would wake up out of a dead sleep because it got so bad at times; Then the abdominal pain started/ Well after my cycle ended I was still in pain and it actually got worse; I got the initial sickness about 4 hours after the booster; Just like a cold; Lymph nodes swollen in my pelvic area; This is a spontaneous report from a contactable reporter (other healthcare professional). The reporter is the patient. A 24-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in right arm, administration date 26Jan2022 at 16:00 (Lot number: FJ5683) at the age of 24 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Hypothyroidism" (unspecified if ongoing) and "Allergy to chemicals" (unspecified if ongoing), notes: Known allergies: Febreeze. Concomitant medication included: LEVOTHYROXINE. Vaccination history included: Covid-19 moderna vaccine (DOSE NUMBER UNKNOWN, SINGLE; Lot number: UNKNOWN), for COVID-19 immunisation, reaction: "Allergic reaction" and Covid-19 vaccine (DOSE NUMBER UNKNOWN; MANUFACTURER UNKNOWN), for COVID-19 immunisation. The following information was reported: ILLNESS (non-serious) with onset 26Jan2022, outcome "recovering", described as "I got the initial sickness about 4 hours after the booster"; NASOPHARYNGITIS (non-serious) with onset 26Jan2022, outcome "recovering", described as "Just like a cold"; NAUSEA (non-serious) with onset 09Feb2022 at 20:00, outcome "recovering", described as "I started to feel nauseous out of no where"; SLEEP DISORDER (non-serious) with onset 09Feb2022 at 20:00, outcome "recovering", described as "I started to feel nauseous out of no where, I would wake up out of a dead sleep because it got so bad at times"; ABDOMINAL PAIN (non-serious) with onset 09Feb2022 at 20:00, outcome "recovering", described as "Then the abdominal pain started/ Well after my cycle ended I was still in pain and it actually got worse"; LYMPHADENOPATHY (non-serious) with onset an unknown date in 2022, outcome "recovering", described as "Lymph nodes swollen in my pelvic area". The events "I got the initial sickness about 4 hours after the booster", "Just like a cold", "I started to feel nauseous out of no where", "I started to feel nauseous out of no where, I would wake up out of a dead sleep because it got so bad at times", "Then the abdominal pain started/ Well after my cycle ended I was still in pain and it actually got worse" and "Lymph nodes swollen in my pelvic area" were evaluated at the physician office visit and emergency room visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of illness, nasopharyngitis, nausea, sleep disorder, abdominal pain and lymphadenopathy. Additional information: The patient did not receive any other vaccines within four weeks prior to the COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. It was reported that the patient waited to do anything about it because she was thinking it was related to her monthly period. Well after her cycle ended the patient was still in pain and it actually got worse. So, on 15Feb2022 she was told by her doctor the best bet was to go to the emergency room (ER). While she was there, they did blood work, urine analysis (U/A), Ultrasound and Computed tomography (CT). That was when the physician assistant (PA) said she had Lymph nodes swollen in her pelvic area acting as appendicitis and was more than likely she got it from the Booster since the patient had not been sick for months besides when she got the booster. Since the vaccination, the patient had not been tested for COVID-19.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Abdominal pain
Hospital-Tage
-
Labordaten
Test Date: 20220215; Test Name: CT; Result Unstructured Data: Test Result:UNKNOWN RESULT; Test Date: 20220215; Test Name: Ultrasound; Result Unstructured Data: Test Result:UNKNOWN RESULT; Test Date: 20220215; Test Name: Blood test; Result Unstructured Data: Test Result:UNKNOWN RESULT; Comments: Blood work; Test Date: 20220215; Test Name: Urine analysis (U/A); Result Unstructured Data: Test Result:UNKNOWN RESULT
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Allergy to chemicals (Known allergies: Febreeze); Hypothyroidism
Andere Medikamente
LEVOTHYROXINE
Allergien
-
Vorherige Impfungen
-

VAERS 2124393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CT
Alter
55,0
Geschlecht
M
Eingang
18.02.2022
Impfdatum
17.02.2022
Beginn
17.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chills Headache Hyperhidrosis Pyrexia

Symptomtext

Sudden onset rigorous chills, fever 101.5 F., sweats, and headache.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
09/17/2022 Pfizer FC3182.

VAERS 2123053

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
MA
Alter
46,0
Geschlecht
F
Eingang
18.02.2022
Impfdatum
16.02.2022
Beginn
16.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Pruritus Pyrexia Rash erythematous

Symptomtext

Received booster 2/16/22 Left arm. By approx 3:15pm my neck chest and back were itchy and broke out in Red Rash. By 4pm had fever 101 orally. I am a Nurse practitioner, so i took Liquid Benadryl Q 4-6 hours 2/16 PM until 2/17 pm. 2/18 rash subsided and i continue to take Claritin.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
none.
Aktuelle Erkrankungen
no illness
Vorgeschichte
None
Andere Medikamente
Pantoprazole
Allergien
Sulfa, Levaquin , Shellfish
Vorherige Impfungen
-

VAERS 2119344

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
PA
Alter
37,0
Geschlecht
F
Eingang
17.02.2022
Impfdatum
14.02.2022
Beginn
15.02.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chills Injection site erythema Injection site induration Injection site swelling Injection site warmth Pain Physical examination Pyrexia

Symptomtext

Individual developed body aches, chills, and fever approximately 12 hours after administration of the booster shot. Symptoms continued for 2 days. Individual developed redness at the site of injection which continued to spread over the course of 3 days. Area was warm, hard, and swollen. Individual was prescribed Keflex.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
medical examination
Aktuelle Erkrankungen
NA
Vorgeschichte
NA
Andere Medikamente
birth control
Allergien
NKA
Vorherige Impfungen
-

VAERS 2119308

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
WA
Alter
45,0
Geschlecht
F
Eingang
17.02.2022
Impfdatum
16.02.2022
Beginn
17.02.2022
Tage bis Beginn
1,0
Dosis
2
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Angina pectoris Fatigue Night sweats Pain in extremity

Symptomtext

heart pain along with fatigue, arm pain, and night sweats

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Hashimoto's
Andere Medikamente
wellbutrin XL, Prozac, Synthroid, Zyrtec, Multi-vitamin, Melatonin
Allergien
none
Vorherige Impfungen
-

VAERS 2119018

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
PA
Alter
50,0
Geschlecht
F
Eingang
17.02.2022
Impfdatum
07.02.2022
Beginn
08.02.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chills Contusion Fatigue Injection site bruising Injection site pain Lymph node pain Lymphadenopathy Myalgia

Symptomtext

extreme fatigue, pain at injection site, muscle aches, extreme chills, lymph node swelling size of a lemon that lasted 7 days with pain on a scale of 1-10 at 10, bruising at injection site, bruising around lymph nodes and underside of arm.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
doctor office did not feel need to do anything further and said all side effects were normal.
Aktuelle Erkrankungen
none
Vorgeschichte
cancer, vision issues
Andere Medikamente
multi vitamin, vitamin b12, vitamin d, calcium
Allergien
none known at this time
Vorherige Impfungen
-

VAERS 2116401

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
KS
Alter
25,0
Geschlecht
M
Eingang
16.02.2022
Impfdatum
02.02.2022
Beginn
11.02.2022
Tage bis Beginn
9,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Alanine aminotransferase increased Aspartate aminotransferase increased Blood creatine phosphokinase increased Blood creatinine normal Chromaturia Exercise tolerance decreased Laboratory test abnormal Myalgia Rhabdomyolysis

Symptomtext

rhabdomyolysis 10 days after inj but also complicated by new meloxicam and weight lifting

Weitere VAERSDATA-Felder
Praegender Schweregrund
Myalgia
Hospital-Tage
-
Labordaten
2/14/22 w/u new muscle pain and brown urine CPK 93,400 cr 1.0 AST 643 ALT 115
Aktuelle Erkrankungen
being evaluated for possible inflammatory arthritis. day of vaccine also started meloxicam. felt good so did one day chest exercises weight liftng. 1-2 days later muscle pain and brown urine. Labs CPK >90K confirmed rhabdomyolysis
Vorgeschichte
joint pain, morbid obesity
Andere Medikamente
meloxicam 15 mg qd
Allergien
No
Vorherige Impfungen
-

VAERS 2110506

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
WA
Alter
43,0
Geschlecht
F
Eingang
14.02.2022
Impfdatum
11.02.2022
Beginn
11.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Dizziness Headache Nausea

Symptomtext

Patient was vaccinated with Pfizer (grey cap) Lot: FJ5683, at 1600 on 2/11/2022. This was a booster dose of Pfizer (the client had also received Pfizer for initial vaccine series). At 1605 client reported headache and nausea, which client reported "this happened with each of my other doses too and with blood donation which is why I can't donate anymore". No visible pallor, shakiness, observed. 1611 initially unable to auscultate BP with multiple attempts, SPO2 100% on RA and HR 88. Client declined to lay down stating "laying down makes the pain much worse". Offered apple juice and cold pack placed on back of neck. Client C/O "just a little bit of lightheadedness" at 1616. 1620 able to verify BP 118/72, HR 86, SPO2 100%. Patient allowed to sit, rest, and recuperate. Client did have history of severe allergy and was to be monitored for 30 minutes. At 1630 client still C/O headache and nausea, husband able to verify that appearance was consistent with baseline and RN determined no signs or symptoms of allergic reaction. Education was provided to couple regarding when to seek medical attention and additional symptoms of allergic reaction. Verbal confirmation from client and spouse that they understood instructions. 1636 improved auscultation of BP 116/74, HR 84, SPO2 99%. Client and spouse felt comfortable and departing unassisted from clinic at 1638.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
unknown
Vorgeschichte
unknown
Andere Medikamente
unknown
Allergien
self reports severe allergy; unknown at time of report specific allergen
Vorherige Impfungen
-

VAERS 2110395

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
IN
Alter
44,0
Geschlecht
F
Eingang
14.02.2022
Impfdatum
03.02.2022
Beginn
06.02.2022
Tage bis Beginn
3,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Burning sensation Pruritus Urticaria

Symptomtext

Severe Hives on stomach ,arms, on both legs, Burns and itch

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
no
Vorgeschichte
no
Andere Medikamente
Synthroid Atorvastatin Bupropion
Allergien
NO
Vorherige Impfungen
-

VAERS 2109611

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
SC
Alter
39,0
Geschlecht
F
Eingang
13.02.2022
Impfdatum
13.02.2022
Beginn
13.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Erythema Pruritus Rash macular

Symptomtext

Over course of 10 minutes, patient became red and splotchy on the arms. She had some generalized itching. Monitored for 15 minutes and given 1 dose of Benadryl 25mg orally. Patient stated she took 25mg prior to coming in for vaccination. Patient's husband to drove her to urgent care upon leaving pharmacy.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Unknown
Vorgeschichte
Obesity, thyroiditis
Andere Medikamente
Benadryl (diphenhydramine) 50mg
Allergien
Flu vaccine, Varicella vaccine, Doxycycline, Calcium channel blockers, wasps, caffeine
Vorherige Impfungen
Flu vaccine, Varicella vaccine; details unknown.

VAERS 2108776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
34,0
Geschlecht
M
Eingang
12.02.2022
Impfdatum
13.01.2022
Beginn
01.01.2022
Tage bis Beginn
-
Dosis
UNK
Route/Site
OT / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Chest discomfort Headache Hyperhidrosis Hypoaesthesia Lymphadenopathy Pain Weight

Symptomtext

numbness in my arm; chest feels tight; pretty heavily swollen lymph nodes in my armpit left arm pit same side as injected in; they were tender; woke up in pool of sweat; headache; aches; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 34 year-old male patient received bnt162b2 (BNT162B2), intramuscular, administration date 13Jan2022 (Lot number: FJ5683) at the age of 34 years as dose number unknown (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete but unknown manufacturer), for COVID-19 immunization. The following information was reported: PAIN (non-serious) with onset Jan2022, outcome "unknown", described as "aches"; HEADACHE (non-serious) with onset 13Jan2022, outcome "unknown", described as "headache"; HYPOAESTHESIA (non-serious) with onset 16Jan2022, outcome "recovering", described as "numbness in my arm"; CHEST DISCOMFORT (non-serious) with onset 16Jan2022, outcome "not recovered", described as "chest feels tight"; HYPERHIDROSIS (non-serious) with onset 13Jan2022, outcome "unknown", described as "woke up in pool of sweat"; LYMPHADENOPATHY (non-serious) with onset 15Jan2022, outcome "recovering", described as "pretty heavily swollen lymph nodes in my armpit left arm pit same side as injected in; they were tender". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain, headache, hypoaesthesia, chest discomfort, hyperhidrosis, lymphadenopathy. Additional Information: He got his booster of the Pfizer covid 19 vaccines, last Thursday and had typical side effects. He had aches, headache, woke up in pool of sweat, the following night on Friday night. On Saturday, woke up with some pretty heavily swollen lymph nodes in armpit left arm pit same side as injected in. They were tender, and then the next day Sunday, he woke up with a little bit of numbness in his arm, same left arm, felt as if when you get your BP taken with blood cuff, it restricts the blood flow, it felt like that. Patient reported arm was a little numb kind of felt like when one gets blood like they put the arm cup on to take your blood pressure, it felt like the blood has been strain of it. This could be related or unrelated, his chest feels tight started, Sunday, Monday, and Tuesday. Lymph nodes not as bad, the numbness he was feel it a little bit, not as noticeable today, but still having the chest tightness. He had read about a lot of the side effects, but he didn't see anything about numbness in arm, some site said it could be an allergic reaction to talk to doctor about. The time of the vaccination was reported as probably noon. No prior vaccination (within 4 weeks). He was not taking other medication. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
Test Name: weigh; Result Unstructured Data: Test Result:245; Comments: weigh 245
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2104828

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

mild
Staat
KY
Alter
37,0
Geschlecht
F
Eingang
11.02.2022
Impfdatum
10.02.2022
Beginn
11.02.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain Skin warm Swelling face

Symptomtext

My dermal fillers on the left side of my face are hot and swelling up. It is very painful

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Sulfa
Vorherige Impfungen
-

VAERS 2102095

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
51,0
Geschlecht
F
Eingang
10.02.2022
Impfdatum
02.02.2022
Beginn
08.02.2022
Tage bis Beginn
6,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Burning sensation Exposure to SARS-CoV-2 Rash pruritic

Symptomtext

On 2/02/2022 at approximately 3:30pm, I received a Pfizer booster injection in my left arm. On 02/06/2022 at approximately 2:30pm I suddenly developed an itching, burning rash with bumps of various sizes on my right wrist. Later that same evening I suddenly developed the same rash on my left wrist. I treated the rashes with a cold compress and they subsided. At approximately 9:00am on 02/10/2022 the rashes returned to both wrists and this time also included the palms of both hands and the outer pinky edge of both hands - again with intense itching and burning sensations. On 02/06/2022 at approximately 2:45pm, I called and reported the sudden rash to the advise nurse and was advised to treat it like contact dermatitis (CD) with a follow-up telephone appointment scheduled for 12:00pm on 02/10/2022. I spoke with Dr. and he diagnosed CD. I informed him I strongly disagreed with his diagnosis because I've been quarantined due to COVID exposure so I haven't been outside of my house and I haven't used any new products or ingested any new food or drinks. He still suggested CD / trail and error treatment.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash pruritic
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
Rheumatoid Arthritis
Vorgeschichte
Rheumatoid Arthritis
Andere Medikamente
N/A Stopped taking all medications in 2020
Allergien
N/A
Vorherige Impfungen
-

VAERS 2101603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
PR
Alter
18,0
Geschlecht
F
Eingang
10.02.2022
Impfdatum
13.01.2022
Beginn
13.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Injection site pain

Symptomtext

Patient presented dizziness and pain in the left arm. After 30 min, the patient reports being well and conscious.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
Hypoglycemia
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2101573

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
KY
Alter
47,0
Geschlecht
F
Eingang
10.02.2022
Impfdatum
07.02.2022
Beginn
07.02.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Feeling abnormal Oropharyngeal pain Pain in extremity

Symptomtext

Patient reported a "very sore arm," feeling "funny," and having a "sore throat" 15 minutes after receiving her second COVID vaccine. Advised patient to continue to wait. Checked on patient 20 minutes post vaccine to question her about history of allergies. Patient was not experiencing any trouble breathing or talking. Offered patient water, which she accepted. After 30 minutes post vaccine, checked on patient again to see if symptoms had improved. She said her throat was still sore but still no trouble breathing or talking and no swelling. No signs of anaphylaxis. Patient had actually been talking on her phone. After more time passed, offered patient Benadryl (refused due to possibility of it causing migraine) and calling for an ambulance which was refused. Patient did take some Loratadine that she found in her purse as a precaution. Patient also had a pulse oximeter in her purse which read her oxygen levels 99%. After patient had waited an hour, she was advised on the signs and symptoms of anaphylaxis and to take Benadryl at home if she felt she needed it.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Oropharyngeal pain
Hospital-Tage
-
Labordaten
Patient called 2 days after the event to let us know her throat continued to be sore through the night and the had decided to see an urgent care physician the day following the event. They instructed her to see her allergist.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
CODEINE, FISH, NUTS, RED DYE (MIGRAINE).
Vorherige Impfungen
-

VAERS 2099691

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

mild
Staat
KY
Alter
28,0
Geschlecht
M
Eingang
09.02.2022
Impfdatum
07.02.2022
Beginn
07.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain in extremity Pruritus Rash

Symptomtext

arm pain, itchy, rashes over body

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2099676

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
26,0
Geschlecht
F
Eingang
09.02.2022
Impfdatum
03.02.2022
Beginn
03.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Contusion Full blood count Platelet count Pyrexia

Symptomtext

Severe Bruising / fever .

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
CBC and a platelet count.
Aktuelle Erkrankungen
-
Vorgeschichte
Asthma.
Andere Medikamente
Lamotrigine Gabapentin Albuterol Advair
Allergien
-
Vorherige Impfungen
-

VAERS 2201205

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
-
Alter
50,0
Geschlecht
F
Eingang
08.02.2022
Impfdatum
31.01.2022
Beginn
28.01.2022
Tage bis Beginn
-
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Burning sensation Erythema multiforme Injection site erythema Injection site pain Injection site pruritus Peripheral swelling Pruritus Rash Urticaria

Symptomtext

Rash, ErythemaMultiform, UrticariaPruritus, left deltoid, burns, itches and is painful Narrative: "I noticed my left arm was swollen immediately." "When I got home around 5 pm, I noticed my left arm around the site of the shot was red, itching and painful."

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site erythema
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2203688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
-
Alter
61,0
Geschlecht
F
Eingang
07.02.2022
Impfdatum
02.02.2022
Beginn
03.02.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Headache Tenderness

Symptomtext

headache, arm tenderness Narrative:

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2091656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
75,0
Geschlecht
F
Eingang
05.02.2022
Impfdatum
04.02.2022
Beginn
05.02.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Erythema Peripheral swelling Pruritus

Symptomtext

Morning of 2/5/2021, pt experienced swelling, redness, and itching on right arm

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
eliquis,
Allergien
-
Vorherige Impfungen
-

VAERS 2091526

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
MN
Alter
23,0
Geschlecht
M
Eingang
05.02.2022
Impfdatum
10.01.2022
Beginn
10.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Injection site pain Myalgia

Symptomtext

Patient states that the muscle soreness at the injection site still has not subsided after 3 and 1/2 weeks. I recommended OTC acetaminophen until he is able to see a doctor to assess.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2088683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
33,0
Geschlecht
F
Eingang
04.02.2022
Impfdatum
27.01.2022
Beginn
29.01.2022
Tage bis Beginn
2,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Arthralgia Axillary pain Chills Erythema Headache Lymphadenopathy Myalgia Pyrexia Tenderness

Symptomtext

01/29/2022 two days after my vaccine I began to experience a large swollen lymph node swelling in my right armpit. Came with redness from armpit to breast, 9 out of 10 on pain scale. I also had a fever until the 2nd of February of 102 degrees. lasting about four days long. Ibuprofen did not take away the pain. Extreme muscle and joint pain, chills, headache. It took about four days for it to go down, and as of today one week post symptoms swelling and redness have gone away including pain and tenderness.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Arthralgia
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2083296

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
WA
Alter
30,0
Geschlecht
M
Eingang
02.02.2022
Impfdatum
27.01.2022
Beginn
27.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness

Symptomtext

Client was here for his first dose of Pfizer (lot number FJ5683, received to the LD at 1547 on 1-27-2022). Shortly after vaccination he complained of feeling dizzy. He did not present with pallor or diaphoresis and no LOC was noted. He denied vision or hearing changes. He reported that he?d been stressed all day and hadn?t had anything to eat or drink yet. He accepted juice and water and drank both without difficulty. At 1600, he laid down (after encouragement) and reported that he felt much better. VS at 1600 were: BP 120/80 laying, HR 64, SPO2 97% on RA. He was allowed to rest/recuperate and continued to drink juice (after encouragement). VS at 1607: BP 118/76 laying, HR 77, SPO2 98% RA. At 1610, he sat at the edge of the cot without difficulty and reported that he felt ?normal?. His BP at this time was 124/84 sitting, HR 81, SPO2 99%. At 1612, he stood and reported that he had no further dizziness. At 1612, his BP standing was 118/84, his HR was 89, and his SPO2 is 100% RA. He and his companion were provided education on vasovagal reactions, what to watch for, and when to seek out medical care. The client was also encouraged to make sure he has adequate fluid and food intake before injections and let his next vaccinator know that he had this reaction for his first dose. Both verbalized understanding. The client reports that he will be monitored through the rest of the day and his companion will drive home. The client remained under observation without further reoccurrence of symptoms until 1621. He reported that he felt ?100% normal?. His VS at this time were: BP 118/84 standing, HR 83, SPO2 100% on RA. He stood and walked around the clinic without difficulty and without requiring assistance. He exited the facility at 1622 with his companion in a private vehicle.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Unknown
Vorgeschichte
Unknown
Andere Medikamente
Unknown
Allergien
Unknown
Vorherige Impfungen
-

VAERS 2083291

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NY
Alter
44,0
Geschlecht
F
Eingang
02.02.2022
Impfdatum
28.01.2022
Beginn
30.01.2022
Tage bis Beginn
2,0
Dosis
3
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Disorientation Dizziness Fatigue Headache Injection site pain Muscular weakness Vertigo

Symptomtext

Vertigo, disorientation, and dizziness beginning late night of 1/29, early morning of 1/30 and continuing to date. Also headache, fatigue, muscle weakness, and pain at injection site directly following injection.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
None. Requesting appointment with MD for 2/3, if available.
Aktuelle Erkrankungen
Flu-like symptoms approximately one and a half weeks prior to vaccination
Vorgeschichte
No
Andere Medikamente
Meloxicam 15 mg (48 hours prior) Methocarbamol 500 mg (48 hours prior)
Allergien
Epinephrine Vicodin Juniper Berries
Vorherige Impfungen
Previous doses of Pfizer Vaccine resulted in flu-like symptoms, rapid heartbeat, headache, and anxiety

VAERS 2082949

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
-
Alter
50,0
Geschlecht
F
Eingang
02.02.2022
Impfdatum
02.02.2022
Beginn
02.02.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Immediate post-injection reaction Throat irritation Urticaria

Symptomtext

Immediately after receiving Pfizer booster to right arm patient started to have itching in her throat, some hives noted to left of neck. Patient was able to swallow water. She was given Benadryl 25 mg 1 tab orally. States is feeling fine approximately 5 minutes. She did wait her total of 15 minutes and went back to work.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2076897

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj5683

mild
Staat
IL
Alter
33,0
Geschlecht
M
Eingang
31.01.2022
Impfdatum
01.01.2022
Beginn
31.01.2022
Tage bis Beginn
30,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Injection site pruritus Injection site urticaria

Symptomtext

Localized hive/itching around injection site. No warmth to skin. No respiratory reaction. No other reactions. Diphenhydramine 50mg oral tablets given. Medication helpful with hive/itching. Patient stated no issues breathing or any other symptoms.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Injection site pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Diphenhydramine 50mg oral tablet
Allergien
Spider bite (unknown species) hives
Vorherige Impfungen
-

VAERS 2076065

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
OR
Alter
14,0
Geschlecht
F
Eingang
31.01.2022
Impfdatum
13.01.2022
Beginn
14.01.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Illness Pyrexia Vaginal ulceration

Symptomtext

Fever and severe illness for 5 days which included vaginal ulcerations. This Covid vaccine was given at the same time as the Influenza vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pyrexia
Hospital-Tage
-
Labordaten
Consults to dermatology and genecology.
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2075050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
-
Alter
39,0
Geschlecht
F
Eingang
30.01.2022
Impfdatum
21.01.2022
Beginn
26.01.2022
Tage bis Beginn
5,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Erythema Pruritus Skin reaction

Symptomtext

Skin reaction at old BCG injection site. Itchy, redness

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
Amlodipine
Allergien
-
Vorherige Impfungen
-

VAERS 2074351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
PA
Alter
13,0
Geschlecht
M
Eingang
29.01.2022
Impfdatum
09.01.2022
Beginn
01.01.2022
Tage bis Beginn
-
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abdominal pain upper Body temperature Chills Fatigue Oropharyngeal pain Pain Pain in extremity Pyrexia

Symptomtext

chills; fatigue; sore arm; fever of 99.1; body aches; stomachache; sore throat; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 13 year-old male patient received bnt162b2 (BNT162B2), administration date 09Jan2022 11:00 (Lot number: FJ5683) at the age of 13 years as dose number unknown (booster), single for covid-19 immunisation. Relevant medical history included: "FPIES" (unspecified if ongoing), notes: FPIES. The patient's concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Manufacturer Unknown), for COVID-19 Immunization. The following information was reported: CHILLS (non-serious) with onset Jan2022, outcome "unknown", described as "chills"; FATIGUE (non-serious) with onset Jan2022, outcome "unknown", described as "fatigue"; PAIN IN EXTREMITY (non-serious) with onset Jan2022, outcome "unknown", described as "sore arm"; PYREXIA (non-serious) with onset Jan2022, outcome "unknown", described as "fever of 99.1"; PAIN (non-serious) with onset Jan2022, outcome "unknown", described as "body aches"; ABDOMINAL PAIN UPPER (non-serious) with onset Jan2022, outcome "unknown", described as "stomach ache"; OROPHARYNGEAL PAIN (non-serious) with onset Jan2022, outcome "unknown", described as "sore throat". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Male 13 year old patient, experienced chills, fatigue, sore arm, fever of 99.1, and body aches, stomach ache and sore throat after receiving booster Covid 19 vaccine on 09Jan2022. Follow-up attempts are completed. No further information is expected. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Abdominal pain upper
Hospital-Tage
-
Labordaten
Test Date: 202201; Test Name: fever; Result Unstructured Data: Test Result:99.1
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Food protein-induced enterocolitis syndrome (FPIES)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2069251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NY
Alter
22,0
Geschlecht
M
Eingang
27.01.2022
Impfdatum
27.01.2022
Beginn
27.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Feeling cold Pallor

Symptomtext

A 21-year-old male patient with no PMH received his 1st Pfizer COVID-19 vaccine. Approximately 3 minutes after the vaccine, he felt "dizzy" and "cold." Patient admitted he was scared and anxious before getting the vaccine. Denied any other symptom. Patient evaluated by on-site EMS and MD. On physical exam noted to be pale. AAOx3. Initial VS: HR 48, RR 16, SpO2 98% and BP 90/40. Lungs with clear breath sounds bilaterally. Patient placed on the stretcher in supine position with raised lower extremities. He drank 8 ounces of water. After 30-minute observation, patient felt better. VS noted with improvement (last set showed HR: 66 RR 16, SpO2 98%, BP: 114/74). Patient had complete resolution of symptoms and was discharged home.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2066958

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
65,0
Geschlecht
M
Eingang
26.01.2022
Impfdatum
21.01.2022
Beginn
21.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja
Activated partial thromboplastin time normal Angiogram cerebral Anticoagulant therapy Arteriogram carotid abnormal Blindness unilateral Blood chloride increased Blood creatinine increased Blood urea increased Carotid artery stenosis Computerised tomogram head Dizziness Echocardiogram Full blood count abnormal Haematocrit decreased Hemianopia homonymous Magnetic resonance imaging head Metabolic function test abnormal Muscular weakness

Symptomtext

transient multiple neurologic symptoms, suggestive of TIA event. Aboout 3 hours following vaccination the patient reported that he noticed some dizziness, left arm weakness, and right homonymous hemianopsia. The patient adamantly denied loss of vision within just one eye and, with directed questioning, reported that he could only see the left side of his visual field, with the right side being dark. He was very adamant that the deficits affected the right visual field. His left arm was weak, but not his left leg. Again, he was adamant that it was his left arm and that the right extremities were unaffected. He could not recall if he had any facial droop and was not sure if he had any dysarthria. He did not have have expressive or receptive aphasia. He was able to call his sister and speak with her by phone. She was able to come and bring him to the hospital. His symptoms lasted about 2 hours and have completely resolved. He has had no stroke or TIA symptoms previously. The patient's symptoms did not localize to one hemisphere or distribution. The patient had extensive evaluation, including head CT scan, CTA head and neck, and carotid duplex, and MRI brain. Moderately severe left carotid stenosis was noted on CTA angiogram, unclear if this is symptomatic as recent symptoms do not all seem attributable to the left ICA/MCA distribution. Carotid duplex demonstrated findings suggestive of high grade left carotid stenosis, with PSV of > 521 cm/s and ICA/CCA ratio of 4.6. Patient had been on chronic aspirin therapy but had stopped < 3 days ago due to getting ready for right hip arthroplasty.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
1,0
Labordaten
1/21/2022 Labs CBC WBC 13.7, hematocrit 37.8 CMP Cr 1.53 (slight elevation from usual), BUN 39, Cl 113, COVID 19 negative PTT wnl, Troponin I wnl Imaging results as above CT angiogram head and neck 1/21 Carotid US 1/22 Echocardiogram 1/22 MRI brain 1/22
Aktuelle Erkrankungen
Fungal balanitis
Vorgeschichte
H/o MI, CAD s/p CABG x 3, low back pain with sciatica, htn, bipolar, cervical radiculopathy, OSA, hyperlipidemia,
Andere Medikamente
Tamsulosin, hydrocodone, lisinopril, clotrimazole topical, lidocaine patch, metoprolol, atorvastatin, ibuprofen, diclofenac gel, aspirin
Allergien
gabapentin, hydrochlorothiazide,
Vorherige Impfungen
-

VAERS 2066057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

mild
Staat
IN
Alter
45,0
Geschlecht
F
Eingang
26.01.2022
Impfdatum
22.01.2022
Beginn
22.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Computerised tomogram Fatigue Kidney infection

Symptomtext

tired, kidney infection

Weitere VAERSDATA-Felder
Praegender Schweregrund
Fatigue
Hospital-Tage
-
Labordaten
ct scan
Aktuelle Erkrankungen
covid
Vorgeschichte
-
Andere Medikamente
lyrica, diclofanoa, lexipro, vitamin d,
Allergien
amoxicillin
Vorherige Impfungen
-

VAERS 2065363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
VA
Alter
28,0
Geschlecht
F
Eingang
26.01.2022
Impfdatum
20.01.2022
Beginn
21.01.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chills Erythema Fatigue Headache Injection site reaction Pain Pyrexia Swelling Urticaria

Symptomtext

Injection site reaction, red swollen welt about the size of a silver dollar, headache, body aches, chills, low grade fever, hives on bilateral legs, chest, back, wrists, and back of neck, and extreme fatigue.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
n/a
Vorgeschichte
Asthma, Scoliosis
Andere Medikamente
Nuva-Ring
Allergien
n/a
Vorherige Impfungen
-

VAERS 2061949

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
49,0
Geschlecht
F
Eingang
25.01.2022
Impfdatum
14.01.2022
Beginn
14.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Axillary pain Immunisation Swelling

Symptomtext

Sore swollen right arm pit; Sore swollen right arm pit; Dose received: 3; This is a spontaneous report from a non-contactable reporter (consumer or other non-HCP). The reporter is the patient. A 49-year-old female patient (not pregnant) received bnt162b2 (BNT162B2), administered in arm right, administration date 14Jan2022 (Lot number: FJ5683) at the age of 49 years as dose 3 (booster), single for COVID-19 immunisation. Relevant medical history included: "Breast cancer" (unspecified if ongoing) and "Blood pressure high" (unspecified if ongoing), notes: High blood pressure. Concomitant medications included: LISINOPRIL; ANASTROZOLE; CALCIUM, CLARITON and VITAMIN D3. Vaccination history included: Bnt162b2 (DOSE 1, SINGLE; Lot number: ELA262; Anatomical site: Right arm; Route of administration: Unspecified), administration date: 09Feb2021, when the patient was 48 years old, for COVID-19 immunisation and Bnt162b2 (DOSE 2, SINGLE; Lot number: ENG199; Anatomical site: Right arm; Route of administration: Unspecified), administration date: 04Mar2021, when the patient was 48 years old, for COVID-19 immunisation. The following information was reported: IMMUNISATION (non-serious) with onset 14Jan2022, outcome "unknown", described as "Dose received: 3"; AXILLARY PAIN (non-serious) with onset 16Jan2022, outcome "not recovered", described as "Sore swollen right arm pit"; SWELLING (non-serious) with onset 16Jan2022, outcome "not recovered", described as "Sore swollen right arm pit". Therapeutic measures were not taken as a result of axillary pain and swelling. Additional information: The patient had no known allergies. 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-19 vaccine. The events did not result in doctor or other healthcare professional office/clinic visit, emergency room/department or urgent care. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Axillary pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Blood pressure high (High blood pressure); Breast cancer.
Andere Medikamente
LISINOPRIL; ANASTROZOLE; CALCIUM; CLARITON; VITAMIN D3.
Allergien
-
Vorherige Impfungen
-

VAERS 2059348

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
17,0
Geschlecht
F
Eingang
24.01.2022
Impfdatum
22.01.2022
Beginn
22.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Induration Pain in extremity

Symptomtext

left arm painful induration

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain in extremity
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2058090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

mild
Staat
NY
Alter
50,0
Geschlecht
F
Eingang
23.01.2022
Impfdatum
21.01.2022
Beginn
21.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Cough Nausea Throat tightness

Symptomtext

CLIENT TAKEN TO EMS TENT DUE TO HISTORY OF SUNCOPE WITH INJECTIONS; FEW MINUTES FOLLOWING VACCINATION CLIENT REPORTED TIGHTNESS IN THROAT, NAUSEA AND COUGHING. NP ON SITE ADMINISTERED BENADRYL 25 MG LIQUID ORALLY. VITAL SIGNS AND HEART MONITORED. NOTIFIED SPOUSE OF SITUATION. CLIENT MONITIRED FOR 1 HOUR BUT REFUSED ANY FURTHER CARE OR TRANSPORT TO HIGHER LEVEL OF CARE. SYMPTOMS RESOLVED. CLIENT LEFT ON OWN AND AGREED TO SEEK ADDITIONAL CARE IS ANY SYMPTOMS RETURN.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Nausea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
unkn
Vorgeschichte
unkn
Andere Medikamente
unkn
Allergien
TREENUT ALLERGY
Vorherige Impfungen
-

VAERS 2055545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

mild
Staat
CA
Alter
24,0
Geschlecht
F
Eingang
21.01.2022
Impfdatum
14.01.2022
Beginn
18.01.2022
Tage bis Beginn
4,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Eczema Erythema Rash Rash pruritic Rash vesicular Skin exfoliation

Symptomtext

Patient received Pfizer booster shot on 1/14/22. Patient reports developing a rash on 1/18/22 on inner arm that eventually spread and "loops" around the arm. Patient also reports the area being flaky, red, a little blistery, and flat. Initially, rash was itchy and then stopped. Patient reported event on 1/19/21 and said her rash was starting to clear up. She also did mention that this may be her eczema, but she was not sure and wanted to report this event.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
no known illness day of vaccination
Vorgeschichte
long term health problem with lung disease or asthma
Andere Medikamente
none known at pharmacy
Allergien
none
Vorherige Impfungen
unknown adverse event

VAERS 2055488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

mild
Staat
PA
Alter
15,0
Geschlecht
M
Eingang
21.01.2022
Impfdatum
17.01.2022
Beginn
17.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chest discomfort Rash Throat irritation

Symptomtext

Mother stated at 7 pm patient got a rash on upper body which progressed to the lower extremities. Then patient had chest heaviness and throat irritation . Mother said began giving benadryl and using albuterol inhaler. Called to have him seen at Urgent Care/ER but was told it could take until morning to be seen if he wasn't severe because of heavy case loads. Mother continued at home monitoring and treatment and symptoms resolved.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Rash
Hospital-Tage
-
Labordaten
No testing down. Mother did not report symptoms to pharmacy until 1/21/22
Aktuelle Erkrankungen
unknown
Vorgeschichte
asthma and Juvenile rheumatoid arthritis
Andere Medikamente
Flovent inhaler
Allergien
seasonal and undetermined food allergies reported by mother
Vorherige Impfungen
-

VAERS 2054539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

mild
Staat
NV
Alter
28,0
Geschlecht
F
Eingang
21.01.2022
Impfdatum
16.01.2022
Beginn
19.01.2022
Tage bis Beginn
3,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pruritus

Symptomtext

per patient after 72 hours from getting the vaccine on 1/19 she experienced severe itchiness all over her body , no sign of hives or redness , no fever , it lasted almost the whole day , pt called me on 1/20 to report the reaction the itchiness was getting better ,

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
-
Allergien
none
Vorherige Impfungen
-

VAERS 2050912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
PR
Alter
44,0
Geschlecht
M
Eingang
20.01.2022
Impfdatum
10.01.2022
Beginn
11.01.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Vaccination site abscess Vaccination site erythema Vaccination site induration Vaccination site pain Vaccination site warmth

Symptomtext

44 y/o male presents to clinic 10 days after booster dose of Pfizer vaccine with an abscess around vaccination site. Infectious process began day after being vaccinated and has progressively worsened. At the moment area presents with erythema, warmth, tenderness on palpation, and enduration. Abscess is not purulent at the moment, and measures approximately one inch. Recommendation was made to visit his primary physician so that he may ordered approriate tests and comence patient on appropriate treatment.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Vaccination site pain
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2048391

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
WA
Alter
26,0
Geschlecht
F
Eingang
19.01.2022
Impfdatum
12.01.2022
Beginn
12.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Anxiety Discomfort Dizziness Feeling abnormal Hypoaesthesia Hypoaesthesia oral Lethargy Limb discomfort Oropharyngeal discomfort Respiratory rate increased Sensation of foreign body

Symptomtext

Patient was present at the clinic on 1/12/2022 for her first dose of Pfizer (lot FJ5683, received to the LD at 1142). At 1148, the client c/o L arm numbness that improved with movement. She then c/o that the tip of her tongue was numb and she c/o of circumoral numbness. No swelling or rash was noted upon visual assessment. She was offered benadryl by responding RNs, but she declined medication. No respiratory distress or discomfort was noted. At 1153, the client appeared slightly lethargic and reported that she felt lightheaded. At approximately 1205, this writer was alerted to assist. At 1205, the client was assisted to lie down on the cot and reported that her s/s of lethargy/lightheadedness were improved upon laying down. Her VS at 1205 were: BP 118/82 laying, HR 104, SPO2 98% RA, T 97.9, RR 16. At 1208, the client reported feeling like ?there is something in my throat?, no swelling or rash noted to face, lips, tongue. Oral mucosa appeared WNL. The client was provided juice and water and was able to drink and speak without difficulty. No respiratory distress was noted. VS at this time were: BP 108/70 laying, HR 91, SPO2 99% RA, RR 16. At 1210, the client reported no changes with numbness sensation to her nose, circumoral area, or the feeling of ?strangeness? to throat. She remained A+O and her respiratory status was WNL. At 1215, the client reported that the ?heaviness? in her throat was going away, but that her nose and circumoral area continued to be numb. She was resting comfortably with no sign of distress or discomfort. VS at 1218: BP 104/66, HR 84, SPO2 97% RA, RR 16. She continued to display no s/s rash/swelling to face, lips, tongue/oral mucosa, throat, arms, or abdomen upon visualization. At 1220, the client reported that she felt dizzy again and that she felt ?weightless?, but that circumoral and tip-of-the-nose numbness had improved (stating ?I don?t feel it at all.?). She reported the weightless feeling had extended to her extremities. VS at 1223: BP 106/68, HR 83, SPO2 99% on RA, RR 16. No LOC, change in consciousness was noted. The client was able to converse in full sentences and drink fluids without difficulty. At 1225, the client reported that the sensation of weightlessness had improved, but her chin was numb and that the numbness to her nose was returning. She then reported that her limbs felt heavy instead of light. At 1229, this writer placed a call to the provider on call, giving a report of the events, vitals, and assessments so far. The provider stated that he doubted this reaction was allergic in nature and that the client was most likely responding to sensations and changes triggered by anxiety, including classic features such as tingling of nose, hands, and lips caused by changes in pH s/t increased respirations. He reported that she should feel comfortable receiving her second dose and that she would be safe to go home, as long as someone could remain with her throughout the day and could call 911 if needed. This writer communicated the provider?s response to the client and her brother (who would remain with her throughout the day). Both were provided education on what to watch for and when to seek out medical care, both verbalized understanding. The client reported that she felt ready to go home and that she would seek out advice from her own personal physician as well. VS at 1235: BP 108/70 sitting, HR 81, SPO2 100% RA, RR 16. The client exited the clinic at 1240, accompanied by her brother.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
Unknown
Vorgeschichte
Unknown
Andere Medikamente
Unknown
Allergien
Unknown
Vorherige Impfungen
-

VAERS 2048093

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
WI
Alter
15,0
Geschlecht
M
Eingang
19.01.2022
Impfdatum
15.01.2022
Beginn
15.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Malaise Nausea Pain Swelling

Symptomtext

It started the same night of the vaccination, Pain was by his collarbone and a lot of nausea, He had me feel one spot on the left side and I felt a big lump. He wasn't feeling well on Sunday and Monday, so On Tuesday Morning 01/18/2022 I decided to take him into the Urgent care because he had one lump on each side of his neck. Doctors said to watch for any lymph nodes under his arm, Patient came home from school today complaining of pain again from his collarbone (left)

Weitere VAERSDATA-Felder
Praegender Schweregrund
Malaise
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
Asthma, ADHD, ASD and Anxiety.
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2047756

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
TX
Alter
74,0
Geschlecht
M
Eingang
19.01.2022
Impfdatum
18.01.2022
Beginn
18.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja
Blood glucose normal Nasopharyngitis Unresponsive to stimuli Vomiting

Symptomtext

0940 RN reviewed pre-vaccination checklist. Reviewed precautions with patient. 0945 RN gave vaccine. Immediately asked how he was doing, he said he was "fine". Moved patient to waiting area and wife waiting with him. 0953 Wife notified called nurse for help, nurse noted he was "zoned out" with eyes open, unresponsive, and cold. Vital signs taken, blood pressure 86/54, pulse 99, Oxygen saturation machine unable to read. Rapid Response Team was called. He was given sternal rub, and patient responded. Glucose checked via finger prick, 139. Alert patient was given juice. He vomited immediately after. 0957 Rapid Response Team arrived. Taken to emergency room.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Vomiting
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Fatigue, legs weak. Presented to vaccine clinic in hospital volunteer wheelchair.
Vorgeschichte
paroxysmal atrial fibrillation, COPD, type 2 diabetes mellitus complicated by neuropathy, hypertension, and hyperlipidemia.
Andere Medikamente
MEDS:, verified with patient INSULIN,DETEMIR,HUMAN 100 UNIT/ML INJ INJECT 20 UNITS UNDER THE SKIN EVERY DAY FOR DIABETES. ONCE OPENED USE APIXABAN 5MG TAB TAKE ONE TABLET BY MOUTH TWICE A DAY FOR BLOOD THINNING. CALL ASPIRIN 81MG EC T
Allergien
Lisinopril- Cough
Vorherige Impfungen
-

VAERS 2043519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj5683

mild
Staat
MN
Alter
31,0
Geschlecht
F
Eingang
18.01.2022
Impfdatum
15.01.2022
Beginn
16.01.2022
Tage bis Beginn
1,0
Dosis
UNK
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Pain Pharyngeal swelling Swelling Swollen tongue Tenderness

Symptomtext

Swollen bump on left side collarbone. Moveable and tender to the touch. Pain when moving arm around bump area. Slightly enlarged tongue and throat. Appeared morning after shot (Sunday morning). Major body aches and pains all day on Sunday. Mouth and throat better on Monday. Collar bone bump still there on Tuesday after shot.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pain
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2037973

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NJ
Alter
14,0
Geschlecht
F
Eingang
15.01.2022
Impfdatum
15.01.2022
Beginn
15.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness Nausea

Symptomtext

Reported nausea and feeling light headed post vaccine. During medical monitoring x 30 mins symptoms slowly resolved. Released / ambulatory from facility with parent.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
NA
Vorgeschichte
NA
Andere Medikamente
NA
Allergien
NA
Vorherige Impfungen
-

VAERS 2036314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NJ
Alter
13,0
Geschlecht
F
Eingang
14.01.2022
Impfdatum
14.01.2022
Beginn
14.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Dizziness

Symptomtext

447pm - pt complained dizziness. she was alert and calm. vital signs stable patients mother accompanied the patient. patient was lying down with elevation both legs. patient said she felt better later. denied any dizziness. alert and calm, vitals stable. left with her mother.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
lamotorotine 75mg po twice a day for adhd
Allergien
-
Vorherige Impfungen
-

VAERS 2036117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
NY
Alter
14,0
Geschlecht
M
Eingang
14.01.2022
Impfdatum
14.01.2022
Beginn
14.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest discomfort Dizziness Electrocardiogram Feeling abnormal Hypoaesthesia Lethargy Muscular weakness

Symptomtext

D135QW5 3:30pm 1/14/22 At approximately 3:30PM, the minor (14 year-old male) client received his first dose of the Pfizer 12+ vaccine, administered by our vaccinator in his Right Deltoid (IM). The client sat in the observation area with his mother and within three minutes complained of light-headedness. The mother reported that he ate within the hour. The Clinical Lead gave the client a bottle of water and checked his vital signs, which were normal. The client was alert and said ?I don?t feel good?. The Clinical Lead decided to assess the client?s ambulatory status by standing him up with support on both sides when she noticed his legs were weak and that he was lethargic. He was immediately transferred to a stretcher while the clinical lead activated EMS at 3:43PM. While on the stretcher, the patient complained of chest discomfort and numbness to the right extremity. The Clinical Lead continued to monitor the client?s vital signs until EMS arrived. When EMS arrived, at approximately 4PM, they took the client?s vital signs and performed an EKG. They informed the client?s mother that he required further medical evaluation. EMS departed with the client and his mother at approximately 4:15PM to a local Medical Center.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
non
Aktuelle Erkrankungen
not known
Vorgeschichte
Not known
Andere Medikamente
not known
Allergien
not known
Vorherige Impfungen
-

VAERS 2032237

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
51,0
Geschlecht
F
Eingang
13.01.2022
Impfdatum
13.01.2022
Beginn
13.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Lip swelling Throat irritation Tongue pruritus

Symptomtext

12:02-Patient came into Covid Observation Area, 5-10 minutes after receiving Pfizer Booster vaccination, reporting swelling to lips, itching to tongue and throat. Denies any difficulty breathing or swallowing. No swelling noted to face, or tongue. Reports h/o Asthma, lungs clear to auscultation, no wheezing noted. Patient alert and oriented x 4, speaking in completing sentences, no difficulty swallowing. Denies experiencing any of the above symptoms after 1st two doses of Pfizer. 12:03 pm- VS: BP 166/91, HR 85, RR 20, 02 SATs 99% RA, no pain 12:05- Call placed to on call provider, Dr., informed of patient symptoms above. Verbal order obtained by RN, states per Dr. , give Benadryl 50 mg x 1 orally now, continue to monitor for additional 30 minutes and call him back with an update. Verbal order repeated and confirmed. 12:08 pm- Benadryl 50 mg orally given x 1 as ordered. 12:09 pm- VS: BP 151/88, HR 83, RR 20, 02 SATs 98% RA. Will continue to monitor. 12:25 pm- Patient reports lip swelling is the same, itching to tongue resolved and slight itching to throat continues. Denies any difficulty breathing or worsening symptoms. Lungs auscultated, clear, no wheezing noted 12:42- Call placed to Dr. , provided with an update on patient symptoms above. Per Dr. , 98% of events will occur within 1st 30 minutes and if patient symptoms improving, ok to be discharged home with a driver. Also states Benadryl will last 4-6 hours, if symptoms return and are worsening, patient to seek Emergent care. Also states patient can take over the counter Zyrtec or Claritin (less sedating, longer lasting) when she gets home for ongoing symptoms and ok to take Benadryl later this evening if needed. 12:50 pm- Patient discharged home in stable condition. Provided with discharge instructions above, verbalized understanding. Accompanied patient out to bathroom. Patient contacted her son who lives nearby, states he will pick her up as she drove in today.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tongue pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
ADJUSTMENT DISORDER W MIXED ANXIETY AND DEPRESSED MOOD ASTHMA, UNSPECIFIED CORONAVIRUS COVID-19 RULED OUT OBESITY, BMI 30-34.9, ADULT
Vorgeschichte
ADJUSTMENT DISORDER W MIXED ANXIETY AND DEPRESSED MOOD ASTHMA, UNSPECIFIED CORONAVIRUS COVID-19 RULED OUT OBESITY, BMI 30-34.9, ADULT
Andere Medikamente
predniSONE (ORASONE) 20 mg Oral Tab Albuterol (PROAIR/PROVENTIL/VENTOLIN) 90 mcg/actuation Inhl HFAA Albuterol (PROVENTIL/VENTOLIN) 2.5 mg /3 mL (0.083 %) Inhl Neb Soln Albuterol (PROVENTIL/VENTOLIN) 2.5 mg /3 mL (0.083 %) Inhl Neb Soln Alb
Allergien
Pencillin Class
Vorherige Impfungen
-

VAERS 2215736

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
-
Alter
44,0
Geschlecht
F
Eingang
12.01.2022
Impfdatum
05.01.2022
Beginn
05.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Chills Fatigue Myalgia Pyrexia

Symptomtext

Myalgia, Fever, CHILLS; FATIGUE Narrative:

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chills
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2028515

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
51,0
Geschlecht
F
Eingang
12.01.2022
Impfdatum
12.01.2022
Beginn
12.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Erythema Pruritus Scratch

Symptomtext

10:28am- Patient brought into Covid Observation Area after reporting itching to scalp, chest, back and arms 10 minutes after receiving Pfizer booster vaccination. Redness and scratch marks noted to these areas but no visible rash or hives noted. Patient denies any difficulty breathing or itching in throat. Lungs clear to auscultation, no wheezing. No swelling noted to face lips tongue or throat. Patient alert and oriented x 4, able to speak in complete sentences. Patient states she experienced itching after 1st dose Moderna, took Benadryl 25 mg when she got home and itching resolved within 20 minutes. Patient also states she took Benadryl 25 mg prior to 2nd dose Moderna and did not experience any itching after 2nd dose. States she did not take any Benadryl today Accompanied by her husband who drove. 10:30 am- VS- BP 148/93, HR 82, RR 20, 02 99% RA, no pain 10:34 am- Call placed to on call physician informed of patient symptoms above. Verbal order per Dr. to give Benadryl 25 mg capsule x 1 now, continue to observe patient for 30 minutes and call Dr. back in 30 minutes to provide update. Also informed Dr. that patient accompanied by her husband who drove. Verbal order repeated and confirmed. 10:35 am- Benadryl 25 mg capsule x 1 given orally as ordered. 10:38 am- VS: Temp 97.8, BP 149/90, HR 78, RR 20, 02 SATs 98% RA, 11:08 am- VS: BP 130/73, HR 64, RR 20, 02 SATs 99% RA- No further redness or scratch marks noted to chest, arms and back. Patient reports that itching is not completely resolved but improved significantly and that she feels much better. 11:14 am- Call placed to Dr., informed of patient improved symptoms. Per Dr., patient ok to be discharged home and to take Over the Counter Benadryl 25 mg every 6-8 hours as needed as the itching may return. 11:20 am- Informed patient and husband of discharge instructions above, understanding verbalized. Patient discharged home in stable condition.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Pruritus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
See below
Vorgeschichte
ANXIETY CHRONIC SINUSITIS HTN (HYPERTENSION) HX OF CHOLECYSTECTOMY HX OF RENAL CALCULUS HX OF TOTAL HYSTERECTOMY HYPERLIPIDEMIA LARYNGOPHARYNGEAL REFLUX MEMBER REQUEST ANNUAL SCREENING MAMMOGRAPHY, SHARED DECISION MAKING, COUNSELING MIGRAINE SLEEP APNEA, EVALUATION SNORING
Andere Medikamente
PARoxetine (PAXIL) 20 mg Oral Tab Lisinopril (PRINIVIL/ZESTRIL) 2.5 mg Oral Tab Omega-3-DHA-EPA-Fish Oil (FISH OIL) 300-1,000 mg Oral Cap Famotidine (PEPCID) 20 mg Oral Tab hydrOXYzine HCL (ATARAX) 25 mg Oral Tab Cholecalciferol, Vitamin D3
Allergien
Penicillin
Vorherige Impfungen
Experienced similar itching to scalp, chest and back after 1st dose Moderna vaccaination

VAERS 2025910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
CA
Alter
21,0
Geschlecht
M
Eingang
11.01.2022
Impfdatum
11.01.2022
Beginn
11.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Dizziness

Symptomtext

Approximately 10 minutes after the client received his first dose of Pfizer COVID-19 he became dizzy in observation. Client was placed in supine position on the ground and his legs were elevated. Vital signs were taken and patient was monitored by clinical staff. When asked, patient stated that his last meal was at 10:30AM. Client was recovered quickly and was given Gatorade. He was able to sit in a chair under his own power. He was monitored for an additional 30 minutes and assessed by our on-site doctor once again before he left with accompanying girlfriend.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None.
Allergien
No Known Allergies
Vorherige Impfungen
-

VAERS 2024750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
TX
Alter
54,0
Geschlecht
M
Eingang
11.01.2022
Impfdatum
11.01.2022
Beginn
11.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Blood pressure decreased Dizziness

Symptomtext

Nurse in observation area stated to writer that BP decreased 20 minutes after immunization temporarily to 90's systolic and then when back up to 110 systolic . Heart rate was 103 consistently. Individual complained of some dizziness writer was told. Oxygen was 93% on room air. ER offered and individual declined. BP 110 systolic when individual left.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dizziness
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None. He said that physician said to take immunization and he had spoken to him.
Vorgeschichte
Diabetes, anxiety disorder, cervical spondylosis, personality disorder chronic sinusitis, allergies environmental , asthma, allergic rhinitis, obesity, adjustment disorder with depressed mood. Individual confirmed he never required a epiPen due to a severe allergic reaction to anything.
Andere Medikamente
Gabapentin, Insulin ,Albuterol, Atorvastatin, Hydroxyzine, Latanoprost, Naproxen, Budesonide, magnesium oxide, cholecalciferol, tamsulosin, Metformin, ,semaglutide, methocarbamol, lisinopril, finasteride, cyanocobalamin
Allergien
Sulfa Drugs and Penicillin
Vorherige Impfungen
-

VAERS 2021271

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
OR
Alter
28,0
Geschlecht
M
Eingang
10.01.2022
Impfdatum
09.01.2022
Beginn
09.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Headache Pain Urticaria

Symptomtext

I had hives covering over 50% of the body, along with soreness and a headache

Weitere VAERSDATA-Felder
Praegender Schweregrund
Headache
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
Marijuana
Allergien
Gluten
Vorherige Impfungen
-

VAERS 2015577

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

mild
Staat
-
Alter
13,0
Geschlecht
M
Eingang
07.01.2022
Impfdatum
07.01.2022
Beginn
07.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Urticaria

Symptomtext

Hives starting on lower left leg spreading to above the knee. Treated with topical benadryl.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Urticaria
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Migraine headaches
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2670090

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NC
Alter
54,0
Geschlecht
M
Eingang
11.08.2023
Impfdatum
02.02.2022
Beginn
01.04.2023
Tage bis Beginn
423,0
Dosis
3
Route/Site
SYR / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Skin depigmentation Vitiligo

Symptomtext

Vitiligo - clear loss of pigmentation on hands and other places Never had this before. No family history that patient knows of. Waiting for treatment options, dependent on approval by insurance company (which currently is refusing to cover).

Weitere VAERSDATA-Felder
Praegender Schweregrund
Skin depigmentation
Hospital-Tage
-
Labordaten
Visited 8/10/2023. Confirmed via visual inspection by dermatologist.
Aktuelle Erkrankungen
-
Vorgeschichte
Asthma
Andere Medikamente
Advair hfa metoprolol succinate Magnesium Vitamin D
Allergien
Egg allergy Wheat allergy Animal Dander Dust Mites Pollen
Vorherige Impfungen
-

VAERS 2619059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
MI
Alter
66,0
Geschlecht
M
Eingang
21.04.2023
Impfdatum
28.01.2022
Beginn
19.07.2022
Tage bis Beginn
172,0
Dosis
3
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Pfizer 4/8/21 Lot# EW0158; Pfizer 4/29/21 Lot# EW0176; Pfizer 1/28/22 Lot# FJ5683

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
COVID +
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2583341

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
15,0
Geschlecht
M
Eingang
16.02.2023
Impfdatum
08.02.2022
Beginn
22.02.2022
Tage bis Beginn
14,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Electroencephalogram abnormal Juvenile myoclonic epilepsy Myoclonus

Symptomtext

Developed myoclonic jerks several times a week approximately 2 weeks after vaccine. These symptoms continued and eventually patient was diagnosed with Juvenile Myoclonic Epilepsy after an EEG in February, 2023.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Electroencephalogram abnormal
Hospital-Tage
-
Labordaten
February, 2023 EEG c/w JME
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2582019

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

gering
Staat
OH
Alter
-
Geschlecht
F
Eingang
15.02.2023
Impfdatum
25.01.2022
Beginn
-
Tage bis Beginn
-
Dosis
3
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A female patient (not pregnant) received BNT162b2 (BNT162B2), on 11Mar2021 at 13:00 as dose 1, single (Lot number: En6207), in left arm, on 01Apr2021 as dose 2, single (Batch/Lot number: unknown), in left arm and on 25Jan2022 at 13:00 as dose 3 (booster), single (Lot number: fj5683), in left arm for covid-19 immunisation. The patient had no relevant medical history. The patient had no known allergies. Concomitant medication(s) included: ROSUVASTATIN, start date: 01Jan2022, stop date: 29Jan2023. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19 which includes Paxlovid (lot number: Gf1783) from 30Jan2023 to 04Feb2023. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente
ROSUVASTATIN
Allergien
-
Vorherige Impfungen
-

VAERS 2565187

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
59,0
Geschlecht
F
Eingang
22.01.2023
Impfdatum
05.04.2022
Beginn
10.04.2022
Tage bis Beginn
5,0
Dosis
4
Route/Site
SYR / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Biopsy skin abnormal Lichen planus Oral lichen planus Oral soft tissue biopsy

Symptomtext

Lichen Planus - both oral and skin forms

Weitere VAERSDATA-Felder
Praegender Schweregrund
Biopsy skin abnormal
Hospital-Tage
-
Labordaten
both oral and skin biopsies confirmed the diagnosis
Aktuelle Erkrankungen
-
Vorgeschichte
diabetes, high blood pressure
Andere Medikamente
osempic, atenolol, amlodipine, lisinopril, fenofibrate, atorvastatin
Allergien
advil, penicillin
Vorherige Impfungen
-

VAERS 2561410

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NJ
Alter
32,0
Geschlecht
M
Eingang
17.01.2023
Impfdatum
07.07.2022
Beginn
15.12.2022
Tage bis Beginn
161,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

during our covid site visit on 12.15.22. it was discovered that we had a pfizer batch in the frig that was past BUD date. during the investigation they went back through all the covid injections that were given and saw this patients lot number was given past the BUD date. patient has been contacted and revaccination was offered . manufacture was notified and reports were filed pending outcome.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2561403

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NJ
Alter
37,0
Geschlecht
M
Eingang
17.01.2023
Impfdatum
07.07.2022
Beginn
15.12.2022
Tage bis Beginn
161,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

during our covid site visit from on 12.15.22. it was discovered that we had a pfizer batch in the frig that was past BUD date. during the investigation they went back through all the covid injections that were given and saw this patients lot number was given past the BUD date. patient has been contacted and revaccination was offered . manufacture was notified and reports were filed pending outcome.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2561391

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NJ
Alter
36,0
Geschlecht
F
Eingang
17.01.2023
Impfdatum
07.07.2022
Beginn
15.12.2022
Tage bis Beginn
161,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

during our covid site visit from on 12.15.22. it was discovered that we had a pfizer batch in the frig that was past BUD date. during the investigation they went back through all the covid injections that were given and saw this patients lot number was given past the BUD date. patient has been contacted and revaccination was offered . manufacture was notified and reports were filed pending outcome.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2561385

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NJ
Alter
34,0
Geschlecht
F
Eingang
17.01.2023
Impfdatum
07.07.2022
Beginn
15.12.2022
Tage bis Beginn
161,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

during our covid site visit from DOH on 12.15.22. It was discovered that we had a pfizer in the frig past BUD date. during the DOH investigation they went back through all the covid injections that were given and saw this patients lot number was given past the BUD date. patient has been contacted and revaccination was offered. manufacture was notified and reports were filed pending outcome.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2561223

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
73,0
Geschlecht
M
Eingang
16.01.2023
Impfdatum
29.01.2021
Beginn
01.02.2021
Tage bis Beginn
3,0
Dosis
2
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Gait inability Peripheral swelling

Symptomtext

I'VE HAD BACK TROUBLE-BUT 2-1-21 MY LEGS SWELLED. TWICE AS BIG-THE VACCINE SEEMED TO SETTLE IN MY BACK - THE 2ND SHOT MADE WORSE @ THIS TIME I CAN'T WALK!!

Weitere VAERSDATA-Felder
Praegender Schweregrund
Gait inability
Hospital-Tage
-
Labordaten
TALKED TO DR DR ABOVE ABOUT SIDE EFFECTS.
Aktuelle Erkrankungen
-
Vorgeschichte
BAD BACK
Andere Medikamente
GABAPENTIN/SILDENAFIL
Allergien
BACTRIM/CYMBALTA
Vorherige Impfungen
-

VAERS 2558519

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NJ
Alter
29,0
Geschlecht
F
Eingang
12.01.2023
Impfdatum
25.07.2022
Beginn
15.12.2022
Tage bis Beginn
143,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

during our covid site visit on 12.15.22, it was discovered that we had a pfizer batch in the frig past BUD date. During the investigation they went back through all the covid injections that were given and saw this patients lot number was given past BUD date. patient has been contacted and revaccination was offered. manufacture was notified and reports were filed pending outcome.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2552793

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
60,0
Geschlecht
F
Eingang
07.01.2023
Impfdatum
01.02.2022
Beginn
-
Tage bis Beginn
-
Dosis
3
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
COVID-19 Vaccination failure

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team and product quality group. The reporter is the patient. A 61-year-old female patient received BNT162b2 (BNT162B2), on 29Mar2021 as dose 1, single (Lot number: ER2613), on 19Apr2021 as dose 2, single (Lot number: EW0158) and on 01Feb2022 as dose 3 (booster), single (Lot number: FJ5683) at the age of 60 years for covid-19 immunisation. The patient's relevant medical history included: "obesity" (unspecified if ongoing), notes: The only thing she has is obesity. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "got my Pfizer Covid Vaccines and I still got Covid/prescribed Paxlovid". The events "got my pfizer covid vaccines and i still got covid/prescribed paxlovid" required emergency room visit. Therapeutic measures were taken as a result of vaccination failure, covid-19. Consumer reported regarding Paxlovid. Has taken Paxlovid for two days so far. Has trouble swallowing the tablets. Placing that tablet in honey, holding them in her mouth until they dissolve and then swallowing. Has had the Pfizer shots and the booster shots and still got Covid. Was holding the pills in her mouth for a little while until the size went down a little bit, so the pill was thinner. She would do that, then would take the pills out and then swallow it. She called him and said she went to urgent care. During the time of Covid when the whole thing happened, she was on unemployment and was not working. When she was working, she was tested every week. Now suddenly, she gets Covid, so she is shocked.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Obesity (The only thing she has is obesity.)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2531147

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PR
Alter
29,0
Geschlecht
M
Eingang
14.12.2022
Impfdatum
23.11.2022
Beginn
23.11.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect product formulation administered

Symptomtext

Bivalent doses of vaccine are administered, when the second dose of COVID-19 vaccine should have been administered.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect product formulation administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2510801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CO
Alter
73,0
Geschlecht
M
Eingang
17.11.2022
Impfdatum
22.03.2022
Beginn
22.03.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Expired product administered No adverse event

Symptomtext

NO adverse event---product was 5 days post expiration of 3/17

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2475549

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
48,0
Geschlecht
M
Eingang
11.10.2022
Impfdatum
31.03.2022
Beginn
27.09.2022
Tage bis Beginn
180,0
Dosis
3
Route/Site
UN / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt
Cough

Symptomtext

cough

Weitere VAERSDATA-Felder
Praegender Schweregrund
Cough
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2453105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
OR
Alter
72,0
Geschlecht
F
Eingang
21.09.2022
Impfdatum
28.01.2022
Beginn
-
Tage bis Beginn
-
Dosis
3
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Epistaxis

Symptomtext

Nosebleed; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP), Program ID: The reporter is the patient. A 72-year-old female patient received BNT162b2 (BNT162B2), on 28Jan2022 as dose 3 (booster), single (Lot number: FJ5683) at the age of 72 years for covid-19 immunisation. The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing); "Vascular Carotid Surgery", start date: Nov2021 (unspecified if ongoing). Concomitant medication(s) included: CLOPIDOGREL, start date: 2021; LISINOPRIL taken for hypertension, start date: 2021; LASIX [FUROSEMIDE], start date: 2021; LIPITOR, start date: 2021; ASPIRIN 81, start date: 2021. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot Number: EW0191), administration date: 07Jun2021, when the patient was 71-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE; Lot Number: EW0217), administration date: 01Jul2021, when the patient was 71-year-old, for COVID-19 immunization, reaction(s): "Nosebleed", "Vascular Carotid Surgery". The following information was reported: EPISTAXIS (non-serious), outcome "unknown", described as "Nosebleed". Therapeutic measures were taken as a result of epistaxis. Additional information: The patient did not receive any other vaccine within 4 weeks prior to vaccinations. The patient received the first, second, and booster doses of the vaccine. After the second dose and the booster dose the patient had nosebleeds. The reporter wanted to know the information related to the vaccine and blood thinners. It was reported that nosebleed occurred after the patients second dose and booster dose of the vaccine. Stated that it was not severe. The patient would feel something in nose and then when she would blow it there would be blood. Adverse event treatment included Vitamin C, so the patient increased her Vitamin C at that time and the nosebleed went away after several days. It was reported that nosebleed was more after the second dose of the vaccine than the booster dose of the vaccine. When the reporter realized she will probably need a second booster and was thinking somewhat surprised that it happened with the patients booster dose. The patient was on several medications. Initially reported that the patients question was related to Lipitor, which she states she thinks it was a blood thinner. It was reported that blood thinner was Plavix, Clopidogrel; not Lipitor. Clopidogrel was in a pharmacy vial. The reported that Lipitor was an Aspirin, then stated no, maybe it was a Calcium. The reporter reported no further information related to her Lipitor.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Epistaxis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Blood pressure high; Carotid endarterectomy
Andere Medikamente
CLOPIDOGREL; LISINOPRIL; LASIX [FUROSEMIDE]; LIPITOR; ASPIRIN 81
Allergien
-
Vorherige Impfungen
-

VAERS 2427604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NJ
Alter
42,0
Geschlecht
M
Eingang
02.09.2022
Impfdatum
01.09.2022
Beginn
02.09.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered

Symptomtext

None - this is for the reporting of an expired Vaccine given to a patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Asthma and Seizure Disorder
Andere Medikamente
Seroquel, Trazadone, Sertraline
Allergien
No Known Food or Drug Allergies
Vorherige Impfungen
-

VAERS 2427599

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NJ
Alter
52,0
Geschlecht
F
Eingang
02.09.2022
Impfdatum
01.09.2022
Beginn
02.09.2022
Tage bis Beginn
1,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Expired product administered No adverse event

Symptomtext

There is no adverse event - this is to report that an expired vaccine was given to a patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Hepatitis C/Hypertension
Andere Medikamente
Methadone, Vitamin A, Oretic, Lopressor, Catapres, Linsinopril, Naproxen, Zyprexa
Allergien
No known food/drug allergies
Vorherige Impfungen
-

VAERS 2413215

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
-
Geschlecht
F
Eingang
17.08.2022
Impfdatum
06.04.2022
Beginn
01.08.2022
Tage bis Beginn
117,0
Dosis
4
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Vaccination failure

Symptomtext

COVID 19; COVID 19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 70-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 20Jan2021 as dose 1, single (Lot number: EL3247), on 10Feb2021 as dose 2, single (Lot number: EL9269), on 02Oct2021 as dose 3 (booster), single (Lot number: FF2589) and on 06Apr2022 as dose 4 (booster), single (Lot number: FJ5683) for covid-19 immunisation. The patient's relevant medical history included: "OSTEOARTHRITIS" (unspecified if ongoing); "SEASONAL ALLERGIES" (unspecified if ongoing). No known allergies. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Aug2022, outcome "unknown" and all described as "COVID 19". Therapeutic measures were taken as a result of vaccination failure, covid-19.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Osteoarthritis; Seasonal allergy
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2409527

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
64,0
Geschlecht
F
Eingang
12.08.2022
Impfdatum
13.04.2022
Beginn
01.07.2022
Tage bis Beginn
79,0
Dosis
4
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable Consumer. The reporter is the patient. A 64-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 13Apr2022 at 13:15 as dose 4 (booster), single (Lot number: FJ5683) at the age of 64 years for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 18Mar2021 as dose 1, single (Lot number: 001B21A), on 04Apr2021 as dose 2, single (Lot number: 001C21A) and on 30Nov2021 as dose 3 (booster), single (Lot number: 066F21A) for covid-19 immunisation. The patient's relevant medical history included: "Migraines" (unspecified if ongoing); "depression" (unspecified if ongoing); "high blood pressure" (unspecified if ongoing). Concomitant medications included: GABAPENTIN; AMLODIPINE; ATORVASTATIN; BOTOX; CALCIUM; ESCITALOPRAM; FREMANEZUMAB; HYDROCHLOROTHIAZIDE; MAGNESIUM; NARATRIPTAN; SUMATRIPTAN; TYLENOL; VITAMIN D3. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jul2022, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: Still testing positive 9 days after going off Paxlovid. Patient received Paxlovid from 27Jul2022 to 31Jul2022.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Name: Covid-19 Test; Test Result: Positive ; Comments: Still testing positive 9 days after going off Paxlovid
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Blood pressure high; Depression; Migraine
Andere Medikamente
GABAPENTIN; AMLODIPINE; ATORVASTATIN; BOTOX; CALCIUM; ESCITALOPRAM; FREMANEZUMAB; HYDROCHLOROTHIAZIDE; MAGNESIUM; NARATRIPTAN; SUMATRIPTAN; TYLENOL; VITAMIN D3
Allergien
-
Vorherige Impfungen
-

VAERS 2408784

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
49,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
01.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408781

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
45,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
03.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408780

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
58,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
01.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
63,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
15,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
04.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
30,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
04.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
27,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
04.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408774

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
71,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
03.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
AR
Alter
64,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
01.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
13,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
04.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408770

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
44,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
01.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408769

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
17,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408768

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
48,0
Geschlecht
U
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408766

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
14,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408764

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
12,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408763

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
52,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408760

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
34,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408759

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
61,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408758

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
35,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
04.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408757

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
12,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
01.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408755

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
12,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
03.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Product storage error

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408754

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
22,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408753

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
40,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
01.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Product storage error

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
36,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
01.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Product storage error

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408751

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
68,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
04.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Product storage error

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408750

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
18,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
04.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
58,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
04.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Product storage error

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
13,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Product storage error

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408746

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
86,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Product storage error

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
32,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408743

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
12,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
01.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
13,0
Geschlecht
U
Eingang
11.08.2022
Impfdatum
01.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Product storage error

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408740

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
37,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
01.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered Product storage error

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408738

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
62,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
01.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408737

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
67,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2408734

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
75,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
03.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
Hypertension, Hyperlipidemia
Andere Medikamente
-
Allergien
Atarax, Dristan, Inderal
Vorherige Impfungen
-

VAERS 2408732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
65,0
Geschlecht
M
Eingang
11.08.2022
Impfdatum
03.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
Unknown
Andere Medikamente
-
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2408730

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
66,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
4
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, Urgent Care. The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
Diabetes
Andere Medikamente
-
Allergien
Tizanidine
Vorherige Impfungen
-

VAERS 2408728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
31,0
Geschlecht
F
Eingang
11.08.2022
Impfdatum
02.08.2022
Beginn
-
Tage bis Beginn
-
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Expired product administered

Symptomtext

The patient received an expired covid vaccine at an outpatient clinic, The vial expired on 7/31/22 per extended shelf-life. The current process is covid vaccines are shipped to main hospital campus and stored in freezer. The Clinic Manager or designated leader from Urgent Care was picking up covid vaccines weekly or as needed to distribute to Urgent Care clinics. The Clinic Manager would store the vials in the refrigerator at Urgent Care to be ready to use. The nurse would pull vial from refrigerator to administer to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Expired product administered
Hospital-Tage
-
Labordaten
Unknown
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2404261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj5683

gering
Staat
VA
Alter
30,0
Geschlecht
F
Eingang
08.08.2022
Impfdatum
08.08.1991
Beginn
30.03.2022
Tage bis Beginn
11.192,0
Dosis
1
Route/Site
IM / UN
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Alopecia areata

Symptomtext

Patient 1 month after 2nd injection developed Alopecia Areata, had patches of hair loss on exam, less than 25% of hair loss. We are currently treating her with Intralesional steroid injections and topical steroid medication to her scalp twice daily. She has not completely regrown her hair yet, but is still ongoing with treatment.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Alopecia areata
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
None
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2397466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj5683

gering
Staat
NY
Alter
44,0
Geschlecht
F
Eingang
30.07.2022
Impfdatum
27.02.2022
Beginn
-
Tage bis Beginn
-
Dosis
4
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Pfizer/BioNTech start date: 27Feb2022 / Paxlovid Treatment of COVID-19 start date: 10Jul2022; Pfizer/BioNTech start date: 27Feb2022 / Paxlovid Treatment of COVID-19 start date: 10Jul2022; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 44-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 27Feb2022 as dose 4 (booster), single (Lot number: Fj5683) at the age of 44 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Stage 1 Triple Negative Breast Cancer" (unspecified if ongoing). There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Pfizer/BioNTech start date: 27Feb2022 / Paxlovid Treatment of COVID-19 start date: 10Jul2022". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive; Negative; Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical information: There were no other medication in 2weeks. The patient had a cold and sniffles yesterday and woke up this morning to test and after a negative tea it came back positive. The patient had no known allergies. Paxlovid (lot number: 2815223) taken for Treatment of COVID-19. Treatment start date was reported as 10Jul2022. Treatment stop date was reported as 15Jul2022. The information on the batch/lot number for [BNT162B2] has been requested and will be submitted if and when received.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Name: COVID-19 test; Test Result: Positive ; Test Name: COVID-19 test; Test Result: Negative ; Test Name: COVID-19 test; Test Result: Positive
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Breast cancer
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2396050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
VA
Alter
79,0
Geschlecht
F
Eingang
29.07.2022
Impfdatum
13.04.2022
Beginn
01.07.2022
Tage bis Beginn
79,0
Dosis
4
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 79-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 22Jan2021 at 13:15 as dose 1, single (Lot number: EL3246), in left arm, on 12Feb2021 at 12:30 as dose 2, single (Lot number: EL3246), in left arm, on 13Oct2021 at 10:15 as dose 3 (booster), single (Lot number: FP2589), in left arm and on 13Apr2022 at 12:00 as dose 4 (booster), single (Lot number: FJ5683) at the age of 79 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "hypertension" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant) with onset Jul2022, outcome "unknown", COVID-19 (medically significant) with onset Jul2022, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (12Jul2022) positive, notes: Symptoms returned 5 days after completion of Paxlovid treatment. Have continued to test positivity since onset of first positive test on 12Jul2022. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient was taking any other medications/products within 2 weeks of starting COVID-19 treatment. The patient was previously receive a COVID-19 Vaccine. No known allergies reported. No drug as reported and reaction: Allergy. No hospitalization prolonged.; Sender's Comments: Based on the information available a possible contributory role of the suspect BNT162B2 cannot be excluded for the reported events of vaccination failure,covid-19.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Date: 20220712; Test Name: COVID test; Test Result: Positive ; Comments: Symptoms returned 5 days after completion of Paxlovid treatment. Have continued to test positivity since onset of first positive test on 12Jul2022.
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Hypertension
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2387434

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
IL
Alter
32,0
Geschlecht
F
Eingang
24.07.2022
Impfdatum
11.02.2022
Beginn
-
Tage bis Beginn
-
Dosis
4
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 33-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 11Feb2022 as dose 4 (booster), single (Lot number: FJ5683) at the age of 32 years for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "multiple sclerosis." (unspecified if ongoing). There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive, notes: With two test, I was once again positive; (2022) Negative, notes: having two negative test I felt tired again. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical Course: The patient received Anti-viral therapy of Paxlovid from 07Jul2022 to 11Jul2022 for the treatment of COVID-19. No other medication received in 2weeks.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Name: Covid-19 Test; Test Result: Positive ; Comments: With two test, I was once again positive.; Test Date: 2022; Test Name: Covid-19 Test; Test Result: Negative ; Comments: having two negative test I felt tired again
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Multiple sclerosis
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2387283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
WA
Alter
77,0
Geschlecht
F
Eingang
24.07.2022
Impfdatum
06.04.2022
Beginn
-
Tage bis Beginn
-
Dosis
4
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 78-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 23Sep2021 as dose 3 (booster), single (Lot number: FF8839), in left arm and on 06Apr2022 at 13:00 as dose 4 (booster), single (Lot number: FJ5683) at the age of 77 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "DJD" (unspecified if ongoing); "HBP" (unspecified if ongoing); "Reflux" (unspecified if ongoing). Concomitant medication(s) included: LOSARTAN. Past drug history included: Daypro, reaction(s): "Allergy"; Voltaren, reaction(s): "Allergy". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "recovered" (Jul2022) and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (13Jul2022) Positive, notes: Positive, Rapid Covid test on 13Jul2022. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical information: Recurrence of symptoms 5 days after finishing five days of Paxlovid (sinus, congestion, cough sneezing) Positive Rapid Covid test on 13Jul2022. No follow-up attempts are possible. No further information is expected.; Sender's Comments: The efficacy of a drug varies from patient to patient and can be affected by different factors, however a contributory role of the suspect drug BNT162B2 (COMIRNATY) to the reported events Drug ineffective and COVID-19 cannot be ruled out.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Date: 20220713; Test Name: SARS Cov-2 Test; Test Result: Positive ; Comments: Positive Rapid Covid test on 13Jul2022
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Acid reflux (esophageal); Blood pressure high; Degenerative joint disease
Andere Medikamente
LOSARTAN
Allergien
-
Vorherige Impfungen
-

VAERS 2387156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
FL
Alter
71,0
Geschlecht
M
Eingang
24.07.2022
Impfdatum
23.02.2022
Beginn
01.07.2022
Tage bis Beginn
128,0
Dosis
4
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71-year-old male patient received BNT162b2 (BNT162B2), on 12Jan2021 as dose 1, single (Lot number: EL3246), in right arm, on 02Feb2021 as dose 2, single (Lot number: EL9263), in right arm, on 28Aug2021 as dose 3 (booster), single (Lot number: FD8448), in right arm and on 23Feb2022 as dose 4 (booster), single (Lot number: FJ5683) at the age of 71 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Essential hypertension" (unspecified if ongoing); "IBS" (unspecified if ongoing); "Type 2 Diabetes" (unspecified if ongoing); "Tinnitus" (unspecified if ongoing); "HCC Prostate Cancer" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Cephalexin, reaction(s): "known allergies Cephalexin". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Jul2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (05Jul2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient was treated with antiviral drug (Paxlovid) from 25Jun2022 to 29Jun2022 with lot number (FY9918). The patient previously received a COVID-19 Vaccine. No follow-up attempts are required. No further information is expected

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Date: 20220705; Test Name: Covid; Test Result: Positive
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Essential hypertension; Irritable bowel syndrome; Prostate cancer; Tinnitus; Type 2 diabetes mellitus
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2371732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
19,0
Geschlecht
M
Eingang
16.07.2022
Impfdatum
19.02.2022
Beginn
-
Tage bis Beginn
-
Dosis
3
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Gait disturbance Haemoglobin Haemoglobin abnormal Lymphoma Peroneal nerve palsy Red blood cell count Red blood cell count abnormal SARS-CoV-2 test

Symptomtext

Lymphoma; After receiving Mandatory Booster for College red blood cell &hemoglobin counts irregular; After receiving Mandatory Booster for College red blood cell &hemoglobin counts irregular; Now also have stepping gait/drop foot; Now also have stepping gait/drop foot; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 19-year-old male patient received BNT162b2 (BNT162B2), on 19Feb2022 as dose 3 (booster), single (Lot number: FJ5683) at the age of 19 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose Number: 2, Batch/Lot No: EW0179, Location of injection: Arm Left), administration date: 05Jul2021, when the patient was 18-year-old, for Covid-19 Immunization, reaction(s): "Swollen lymph nodes", "mild dry cough"; BNT162b2 (Dose Number: 1, Batch/Lot No: EW0183, Location of injection: Arm Left), administration date: 14Jun2021, when the patient was 18-year-old, for Covid-19 Immunization. The following information was reported: LYMPHOMA (hospitalization, medically significant, life threatening), outcome "not recovered"; RED BLOOD CELL COUNT ABNORMAL (hospitalization, life threatening), HAEMOGLOBIN ABNORMAL (hospitalization, life threatening), outcome "not recovered" and all described as "After receiving Mandatory Booster for College red blood cell &hemoglobin counts irregular"; PERONEAL NERVE PALSY (hospitalization, life threatening), GAIT DISTURBANCE (hospitalization, life threatening), outcome "not recovered" and all described as "Now also have stepping gait/drop foot". The patient was hospitalized for lymphoma, red blood cell count abnormal, haemoglobin abnormal, peroneal nerve palsy, gait disturbance (hospitalization duration: 4 day(s)). The events "lymphoma", "after receiving mandatory booster for college red blood cell &hemoglobin counts irregular" and "now also have stepping gait/drop foot" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Haemoglobin: (unspecified date) irregular, notes: red blood cell & hemoglobin counts irregular; Red blood cell count: (unspecified date) irregular, notes: red blood cell & hemoglobin counts irregular; SARS-CoV-2 test: (Dec2021) Negative, notes: Covid test type post vaccination=Nasal Swab; (Apr2022) Negative, notes: Covid test type post vaccination=Blood Test. Therapeutic measures were taken as a result of lymphoma, red blood cell count abnormal, haemoglobin abnormal. It was unknown if therapeutic measures were taken as a result of peroneal nerve palsy, gait disturbance. Clinical course: Swollen lymph nodes and mild dry cough after 2nd dose. After receiving Mandatory Booster for College red blood cell & hemoglobin counts irregular. Required blood transfusions. Diagnosis is Lymphoma. only treatment is chemotherapy. Now also have stepping gait/drop foot. Adverse event start date Dec2021. It was unknown if any other vaccine in four weeks. The patient did not take any other medications in two weeks. The patient was not infected with covid prior vaccination. The patient was tested for covid post vaccination.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200951237 same patient and product, different dose and different events;

Weitere VAERSDATA-Felder
Praegender Schweregrund
Gait disturbance
Hospital-Tage
4,0
Labordaten
Test Name: hemoglobin counts; Result Unstructured Data: Test Result:irregular; Comments: red blood cell & hemoglobin counts irregular; Test Name: red blood cell; Result Unstructured Data: Test Result:irregular; Comments: red blood cell & hemoglobin counts irregular; Test Date: 202112; Test Name: Covid-19 Test; Test Result: Negative ; Comments: Covid test type post vaccination=Nasal Swab; Test Date: 202204; Test Name: Covid-19 Test; Test Result: Negative ; Comments: Covid test type post vaccination=Blood Test
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Known allergies: No Other medical history: None
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2368995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
66,0
Geschlecht
M
Eingang
14.07.2022
Impfdatum
12.04.2022
Beginn
08.06.2022
Tage bis Beginn
57,0
Dosis
4
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Asthenia COVID-19 Cough Insomnia Nasal congestion SARS-CoV-2 test positive

Symptomtext

It was June 8, 2022 I woke up feeling weak. I tried to lie down but couldn't go to sleep. I had a little cough and nasal congestion. The weakness became less of an issue within hours. The congestion persisted. On June 9, 2022 I took an at home COVID-19 test and it was positive. I called my doctor for advice and was prescribed FLONASE and a decongestant. I was told to stay isolated for as long as necessary. My symptoms have gradually faded out in the last few days. It was not a bad cough. Right now I feel pretty close to normal. The cough lingering until this past weekend, June 8.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Asthenia
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Atorvastatin
Allergien
None
Vorherige Impfungen
-

VAERS 2362381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NE
Alter
29,0
Geschlecht
F
Eingang
08.07.2022
Impfdatum
03.03.2022
Beginn
05.07.2022
Tage bis Beginn
124,0
Dosis
3
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

covid_test_result=Positive; covid_test_result=Positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 24Jun2021 as dose 1, single (Lot number: EW0196), in right arm, on 15Jul2021 as dose 2, single (Lot number: EW0198), in right arm and on 03Mar2022 as dose 3 (booster), single (Lot number: FJ5683) at the age of 29 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: MURO 128; ELDERBERRY [SAMBUCUS NIGRA]; MAGNESIUM; VITAMIN D [COLECALCIFEROL]; TYLENOL. Past drug history included: Gluten, reaction(s): "Known allergies: Gluten", notes: Known allergies: Gluten; Sulfa-based antibiotics, reaction(s): "known allergies: sulfa-based antibiotics", notes: Known allergies: sulfa-based antibiotics; Ibuprofen, reaction(s): "Known allergies: Ibuprofen", notes: known allergies: ibuprofen. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 05Jul2022, outcome "unknown" and all described as "covid_test_result=Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (23Jun2022) Negative, notes: Nasal Swab; (05Jul2022) Positive, notes: Nasal Swab; (21Oct2021) Negative, notes: BioFire Respiratory 2.1-EZ Panel RT-PCR. Nasal Swab. Clinical course: It was reported that, got the COVID vaccine shot 1 and shot 2 right before her period was due. Her cramps were so much more horrible than normal. After shot 1, her period cramps caused her to nearly pass out from the severity of the pain. After shot 2, her period cramps caused her to vomit from the severity of the pain. There were no other obvious changes in her meds, work, sicknesses, diet, exercise, stress, etc. that could have affected her cycle. The patient did not receive any other vaccines within four weeks prior to the vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Date: 20220623; Test Name: Rapid SARS-CoV-2 RT-PCR; Test Result: Negative ; Comments: Nasal Swab; Test Date: 20220705; Test Name: Rapid SARS-CoV-2 RT-PCR; Test Result: Positive ; Comments: Nasal Swab; Test Date: 20211021; Test Name: RT-PCR.; Test Result: Negative ; Comments: BioFire Respiratory 2.1-EZ Panel RT-PCR. Nasal Swab
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
MURO 128; ELDERBERRY [SAMBUCUS NIGRA]; MAGNESIUM; VITAMIN D [COLECALCIFEROL]; TYLENOL
Allergien
-
Vorherige Impfungen
-

VAERS 2362283

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NV
Alter
35,0
Geschlecht
M
Eingang
08.07.2022
Impfdatum
30.04.2022
Beginn
-
Tage bis Beginn
-
Dosis
4
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Drug ineffective HIV test SARS-CoV-2 test

Symptomtext

COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 36-year-old male patient received BNT162b2 (BNT162B2), on 31Dec2021 as dose 3 (booster), single (Lot number: EW0191) and on 30Apr2022 as dose 4 (booster), single (Lot number: FJ5683) at the age of 35 years for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 15Apr2021 as dose 1, single (Lot number: 041B21A) and on 13May2021 as dose 2, single (Lot number: 041B21A) for covid-19 immunisation. The patient's relevant medical history included: "HIV positive" (unspecified if ongoing); "thalassemia minor" (unspecified if ongoing); "Asthma" (unspecified if ongoing); "Known allergies: Shrimp" (unspecified if ongoing). Concomitant medication(s) included: BIKTARVY. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19 Treatment". Pateint received Paxlovid from 28Jun2022 to 02Jul2022 (Lot number: 1916517A). Other medication in 2weeks product: Biktarvy (brand: Gilead, lot number: 031317). Completed Paxlovid rounds yesterday - 01Jul2022. Today 02Jul2022, patient was testing positive. Currently, patient had some stuffiness, sneezing, and random cough. No fever. The patient underwent the following laboratory tests and procedures: HIV test: (unspecified date) positive; SARS-CoV-2 test: (unspecified date) Unknown results; (02Jul2022) positive. Therapeutic measures were taken as a result of drug ineffective, covid-19.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Name: HIV; Test Result: Positive ; Test Name: COVID-19; Result Unstructured Data: Test Result:Unknown results; Test Date: 20220702; Test Name: COVID-19; Test Result: Positive
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Allergy to animal; Asthma; HIV positive; Thalassemia minor
Andere Medikamente
BIKTARVY
Allergien
-
Vorherige Impfungen
-

VAERS 2361206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
53,0
Geschlecht
M
Eingang
07.07.2022
Impfdatum
02.04.2022
Beginn
28.06.2022
Tage bis Beginn
87,0
Dosis
4
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Feeling abnormal SARS-CoV-2 test positive

Symptomtext

Received 4th dose of Pfizer on 04/02/2022, then started feeling bad on 06/27/2022 and thought it was allergies. Started feeling worse as days went by so I took home test on 06/28/2022 and tested positive. Had a telemedicine appt on 06/29/2022. Was prescribed Paxlovid. Feeling better now on 7/7/2022.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Home test - positive
Aktuelle Erkrankungen
NA
Vorgeschichte
Hypertension
Andere Medikamente
Lisinopril; Tadalafil; Truvada; Ciclopirox Olamine; Allegra D; Multivitamin
Allergien
Slightly lactose intolerance; seasonal allergies
Vorherige Impfungen
-

VAERS 2356351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
FL
Alter
69,0
Geschlecht
M
Eingang
03.07.2022
Impfdatum
19.03.2022
Beginn
01.06.2022
Tage bis Beginn
74,0
Dosis
4
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old male patient received BNT162b2 (BNT162B2), on 12Jan2021 as dose 1, single (Lot number: EL1284), in right arm, on 01Feb2021 as dose 2, single (Lot number: EL2263), in right arm, on 31Aug2021 as dose 3 (booster), single (Lot number: FC3184), in right arm and on 19Mar2022 as dose 4 (booster), single (Lot number: FJ5683) at the age of 69 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies:Penicillin" (unspecified if ongoing), notes: Known allergies:Penicillin. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Jun2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (21Jun2022) Positive; (15Jun2022) Negative. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical Information: The patient received vaccine. Anti-viral product included Paxlovid for Treatment of COVID-19 started from 10Jun2022 till 15Jun2022. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Date: 20220621; Test Name: Antigen test; Test Result: Positive ; Test Date: 20220615; Test Name: Home antigen test; Test Result: Negative
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Penicillin allergy (Known allergies:Penicillin)
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2328440

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NJ
Alter
13,0
Geschlecht
M
Eingang
23.06.2022
Impfdatum
07.01.2022
Beginn
18.06.2022
Tage bis Beginn
162,0
Dosis
3
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Contracted COVID-19; Contracted COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 13-year-old male patient received BNT162b2 (BNT162B2), on 24May2021 as dose 1, single (Lot number: EW0175), on 14Jun2021 as dose 2, single (Lot number: EW0187) and on 07Jan2022 as dose 3 (booster), single (Lot number: FJ5683) at the age of 13 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 18Jun2022, outcome "recovering" and all described as "Contracted COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (18Jun2022) Positive, notes: Nasal Swab. Therapeutic measures were not taken as a result of drug ineffective, covid-19. Clinical course: Patient had no covid prior to vaccination.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Date: 20220618; Test Name: FlowFlex; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2318521

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PA
Alter
32,0
Geschlecht
M
Eingang
14.06.2022
Impfdatum
01.01.2022
Beginn
01.05.2022
Tage bis Beginn
120,0
Dosis
3
Route/Site
- / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 32-year-old male patient received BNT162b2 (BNT162B2), on 05Mar2021 as dose 1, single (Lot number: Ew0172), in right arm, on 06Apr2021 as dose 2, single (Lot number: Er8737), in right arm and on 17Mar2022 as dose 3 (booster), single (Lot number: FJ5683) at the age of 32 years, in right arm for covid-19 immunisation; diclofenac sodium (DICLOFENAC SODIUM), since 01Jan2022 (Batch/Lot number: unknown). The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "obesity" (unspecified if ongoing). Concomitant medication(s) included: GABAPENTIN, start date: 01Jan2022. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset May2022, latency 2 months 21 days after the suspect product(s) administration, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Jun2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical significance: Patient after taking the Paxlovid and recovering from COVID, he was now experiencing symptoms again and tested positive again. he was currently 6 days post the final dose of the Paxlovid. Patient had no known allergies. No follow-up attempts are possible. No further information is expected. Follow-Up (10Jun2022): Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Date: 202206; Test Name: Testing; Test Result: Positive
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Asthma; Obesity
Andere Medikamente
GABAPENTIN, DICLOFENAC SODIUM
Allergien
-
Vorherige Impfungen
-

VAERS 2312697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
52,0
Geschlecht
F
Eingang
08.06.2022
Impfdatum
17.05.2022
Beginn
18.05.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

I tested positive for Covid on 18May2022; I tested positive for Covid on 18May2022.; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 02Mar2021 as dose 1, single (Lot number: EN5318), in left arm, on 23Mar2021 as dose 2, single (Lot number: EN5318), in left arm and on 17May2022 as dose 3 (booster), single (Lot number: FJ5683) at the age of 52 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. 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. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had been tested for COVID-19. The following information was reported: VACCINATION FAILURE (medically significant) with onset 18May2022, outcome "unknown", described as "I tested positive for Covid on 18May2022"; COVID-19 (medically significant) with onset 18May2022, outcome "unknown", described as "I tested positive for Covid on 18May2022.". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (18May2022) Positive, notes: Nasal Swab. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Date: 20220518; Test Name: BinaxNow; Result Unstructured Data: Test Result:Positive; Comments: Nasal Swab
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: No Known allergies: No
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2280451

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PA
Alter
57,0
Geschlecht
F
Eingang
03.06.2022
Impfdatum
08.01.2022
Beginn
-
Tage bis Beginn
-
Dosis
4
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Drug ineffective SARS-CoV-2 test Vaccination failure

Symptomtext

Positive for Covid after 4 Doses of the Pfizer Covid 19 Vaccines; Positive for Covid after 4 Doses of the Pfizer Covid 19 Vaccines; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group and medical information team, Program ID: (172086). The reporter is the patient. A 58-year-old female patient received BNT162b2 (BNT162B2), on 25Jan2021 as dose 1, single (Lot number: EL9262), on 15Feb2021 as dose 2, single (Lot number: EN5318), on 07Aug2021 as dose 3 (booster), 0.3 ml single (Batch/Lot number: unknown) and on 08Jan2022 as dose 4 (booster), single (Lot number: FJ5683) at the age of 57 years for COVID-19 immunization. The patient's relevant medical history included: "Migraine" (ongoing); "Allergies" (unspecified if ongoing). Concomitant medication(s) included: DEPAKOTE taken for migraine; NEFAZODONE taken for migraine; BENADRYL taken for hypersensitivity; FROVATRIPTAN; TYLENOL. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Positive for Covid after 4 Doses of the Pfizer Covid 19 Vaccines". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (27Apr2022) positive; (02May2022) Negative; (06May2022) Negative; (08May2022) Positive; (17May2022) Negative. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Caller stated she wanted to say that she is a fan of Pfizer and she has had the Pfizer 2 COVID Shots and the 2 Boosters and it was all about it and she wanted Pfizer to get closer to understanding these Variants and Medications. Caller stated her doctor was telling her that testing positive again was not a problem and that she didn't need to quarantine anymore and she knew that couldn't be right, so she wanted to inform people of the correct information. Caller stated on 27Apr2022, she tested positive for COVID. Caller stated her first dose of Paxlovid was in the evening on 27Apr2022 and she took all of them and completed the medication on 02May2022. Caller stated she took all of them and they left the nastiest taste in her mouth, it was so bitter and it lasted for the entire 5 days. Caller stated on 02May2022, she tested negative for COVID, but she still didn't feel super great. Caller stated on 06May2022, she tested for COVID again because she wasn't feeling super great, but it was negative. Caller stated she has a friend that is a nurse and told her she can get rebound, it was brand new info at that time. Caller stated on 08May2022, she got an itchy nose and new symptoms and she tested positive for COVID on that day, ragingly positive. Caller stated she tested everyday and continued testing positive through 16May2022 at which point she tested negative and she confirmed it the next day or 2. Caller stated the symptoms that she had with the first episode of COVID were different than with the second episode of COVID. Caller states she started Paxlovid the same day she tested positive, so she doesn't know if the symptoms were from Paxlovid or COVID. Caller stated that the First Episode she was Lightheaded and Dizzy, she had Flashing in the Periphery of her Vision especially upon waking for 3 days and then it went away. Caller stated these occurred 30Apr, 31Apr, 01May and it may have been another day but it was not as obvious. Caller stated she thought it was weird because she has migraines but not with an aura, so she thought she wondered if she was getting an aura, but it didn't stay the whole day, just a half hour and then it would go away. Caller stated she looked on Read It and some other people had that. Caller stated she also had insomnia, sore throat, and malaise where she would just be laying around, a sniffle or tickle in the nose like allergies, and she was tired. Caller stated she tested negative and then the next day she tested positive. Caller stated with the Rebound Covid, it was all upper respiratory and no insomnia, but super fatigued. Caller states it was like there were 3 stages. Caller stated the First Stage when she was positive for Covid and taking Paxlovid she experienced insomnia, dizziness, and she teaches yoga and has good balance, but she almost fell over in the shower, flashing lights and it was like neurological. Caller stated then the Second Stage when she was testing negative, she would sleep for 10-12 hours a night and need a nap during the day, and she is normally a crappy sleeper. Caller stated that was the in between time, which is why she said she didn't feel better. Caller states she had a cough the whole time. Caller states then the 3rd Stage when she tested Positive for Covid again/Rebound was very much upper respiratory with crushing fatigue but not sleepiness, but she was really tired and apathetic, like she doesn't feel like it and was really demotivated and lazy and unable to concentrate. Caller states she would like to see this happen. Caller states she would like it to be that the doctor calls a patient and tells them they have Covid and they would then ask would you like to help give feedback to Pfizer yes or no and then depending on the answer, he could give them a card or send them to a link, that would provide them with some things they should know or watch for like they did after the Covid injection. Caller states she participated in all of that with the Covid Vaccine and she feels like it is needed with this because the variant it is prescribed for isn't the same variant it is was approved for on 22Dec2021, that was for Delta and we are 4 variants later on Omicron. It was reported that the treatment none, Fluids and Quarantine. This is a notification generated from the gQTS system. As part of the LOE simplification process, the following Complaint Records were classified as Product Use Attributes // Lack of Effect and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process according to in PQS Q1215 and/or Q1252. Refer to the below table for details: Product- Description (CR): COMPOUND BNT162 COVID- 19 VACCINE SUSPENSION FOR INTRAMUSCULAR 2ML MULTIPLE DOSE VIAL X 1. Lot-# (CR): EL9262: Conclusion of Previously Completed Investigation (FCI/SI/OffCI): The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EL9262 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EL9262, fill lot EL9253, and the formulated drug product lot EL9244. A complaint sample was not returned, and photographs were not received. There were no deviations that may have caused a complaint of this nature. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. Product- Description (CR): COMPOUND BNT162 COVID- 19 VACCINE SUSPENSION FOR INTRAMUSCULAR 2ML MULTIPLE DOSE VIAL X 1. Lot-# (CR): EN5318: Conclusion of Previously Completed Investigation (FCI/SI/OffCI): The complaint for lack of effect of the PFIZER BIONTECH COVID-19 VACCINE lot EN5318 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot. The final scope included the reported finished goods lot EN5318, fill lot EN5317, and the formulated drug product lot EN5316. A complaint sample was not returned, and photographs were not received. There were no deviations that may have caused a complaint of this nature. No root cause or corrective/preventative actions were identified as the complaint was not confirmed. All release testing performed prior to the release of the reported batch was within specifications. When more than one investigation is found in the family, the Conclusion field could result in repeating rows for the CR in the table. If the Conclusion is blank in the table above, then the investigation record is likely an Offline Contractor Investigation and the conclusion must be obtained directly from the child investigation record(s) of the linked Complaint Record. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202200696468 Same reporter/patient, different drug/events

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Date: 20220427; Test Name: Covid Test; Test Result: Positive ; Test Date: 20220502; Test Name: Covid Test; Test Result: Negative ; Test Date: 20220506; Test Name: Covid Test; Test Result: Negative ; Test Date: 20220508; Test Name: Covid Test; Test Result: Positive ; Test Date: 20220517; Test Name: Covid Test; Test Result: Negative
Aktuelle Erkrankungen
Migraine
Vorgeschichte
Medical History/Concurrent Conditions: Allergy
Andere Medikamente
DEPAKOTE; NEFAZODONE; BENADRYL; FROVATRIPTAN; TYLENOL
Allergien
-
Vorherige Impfungen
-

VAERS 2306591

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
68,0
Geschlecht
M
Eingang
02.06.2022
Impfdatum
13.04.2022
Beginn
01.05.2022
Tage bis Beginn
18,0
Dosis
4
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

I took a rapid test and also was Positive; I took a rapid test and also was Positive; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68-year-old male patient received BNT162b2 (BNT162B2), in 2021 as dose 1, single (Lot number: FL9264), in left arm, in 2021 as dose 2, single (Lot number: EN6201), in left arm, on 28Sep2021 as dose 3 (booster), single (Lot number: FF2588), in left arm and on 13Apr2022 as dose 4 (booster), single (Lot number: FJ5683) at the age of 68 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "history of sporadic/rare/non-chronic A-fib" (unspecified if ongoing), notes: history of sporadic/rare/non-chronic A-fib. Concomitant medication(s) included: ROSUVASTATIN, start date: 04Nov2019, stop date: 18May2022. Past drug history included: Codeine, reaction(s): "Known Allergies: Codeine", notes: Known Allergies: Codeine. The following information was reported: COVID-19 (medically significant), DRUG INEFFECTIVE (medically significant) all with onset May2022, outcome "unknown" and all described as "I took a rapid test and also was Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (May2022) Negative; (May2022) Positive. Therapeutic measures were taken as a result of covid-19, drug ineffective. Additional information: Serious, Seriousness criteria-Results in death, Seriousness criteria-Life threatening, Seriousness criteria-Caused/prolonged hospitalization, Seriousness criteria-Disabling/Incapacitating, Seriousness criteria-Congenital anomaly/birth defect reported as no. Proprietary medicinal product name: Pfizer/Paxlovid, Batch/lot number: N/A, Indication for use in the case: Treatment of COVID-19, Date of start of drug: 19May2022, Date of last administration: 24May2022. Reported Event: Rebound COVID. Took full course of drug (5 days). Only two side effects: 1) foul metallic taste; 2) difficulty sleeping. By day 5 I felt fine and on day 6 registered neg on at-home antigen test. My wife was one day behind me in cycle and sicker during her illness. She also took Paxlovid and was neg on her day 6. But by her day 7/my day 8 she became sick again with severe headache, fatigue, etc. We went to see doc for help. While there she took a PCR test and was positive again. After we got home I took a rapid test and also was positive. My symptoms initially were mild - worst was bad cough, also sneezing/dripping - and are milder yet on this rebound. Her rebound symptoms are a little less bad than first round but worse than mine; no sore throat as with initial illness but splitting headache. Biggest downside for me is having to redo the 5/5 isolation/masking.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Date: 202205; Test Name: Home antigen test; Test Result: Negative ; Test Date: 202205; Test Name: Rapid COVID-19 test; Test Result: Positive
Aktuelle Erkrankungen
-
Vorgeschichte
Medical History/Concurrent Conditions: Atrial fibrillation paroxysmal (history of sporadic/rare/non-chronic A-fib)
Andere Medikamente
ROSUVASTATIN
Allergien
-
Vorherige Impfungen
-

VAERS 2306409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
76,0
Geschlecht
M
Eingang
02.06.2022
Impfdatum
21.04.2022
Beginn
19.05.2022
Tage bis Beginn
28,0
Dosis
4
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Drug ineffective

Symptomtext

COVID 19 after immunization; COVID 19 after immunization; This is a spontaneous report received from contactable reporter(s) (Physician). The reporter is the patient. A 76-year-old male patient received BNT162b2 (BNT162B2), on 21Apr2022 as dose 4 (booster), single (Lot number: FJ5683) at the age of 76 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 19May2022, outcome "recovering" and all described as "COVID 19 after immunization". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: UNKNOWN, notes: Covid symptoms.Clinical course included anti viral details product COVID 19 Treatment, brand Paxlovid, treatment start date 10May2022, treatment stop date 14May2022, indication Treatment of COVID-19. Adverse event Five days after completing five day course of paxlovid, Covid symptoms returned, mild fever, malaise, cough, congestion. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on the information available and close temporal association, a possible contributory role of the suspect Product cannot be excluded for the reported events . The case will be reassessed once new information is available.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Name: COVID-19; Result Unstructured Data: Test Result:UNKNOWN; Comments: Covid symptoms returned
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2306300

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
65,0
Geschlecht
M
Eingang
02.06.2022
Impfdatum
23.04.2022
Beginn
-
Tage bis Beginn
-
Dosis
4
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Pharmacist). The reporter is the patient. A 66-year-old male patient received BNT162b2 (BNT162B2), on 23Apr2022 as dose 4 (booster), single (Lot number: FJ5683) at the age of 65 years for covid-19 immunisation; covid-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) and other medication in 2 weeks included: LOSARTAN; AMLODIPINE; OMEPRAZOLE; SUCRAFATE; GEMTESA; FINASTERIDE; VITAMIN C [ASCORBIC ACID]; VITAMIN D [VITAMIN D NOS]; B12 [CYANOCOBALAMIN]. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Unknown results; (14May2022) Unknown results, notes: symptoms reoccurred. Therapeutic measures were taken as a result of drug ineffective, covid-19 which included Paxlovid from 07May2022 to 11May2022. Four days after completing therapy, symptoms reoccurred on 14May2022.; Sender's Comments: Based on the information available and close temporal association, a possible contributory role of the suspect Product cannot be excluded for the reported events . The case will be reassessed once new information is available.

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
Test Name: COVID-19 test; Result Unstructured Data: Test Result:Unknown results; Test Date: 20220514; Test Name: COVID-19 test; Result Unstructured Data: Test Result:Unknown results; Comments: symptoms reoccurred
Aktuelle Erkrankungen
-
Vorgeschichte
Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
Andere Medikamente
LOSARTAN; AMLODIPINE; OMEPRAZOLE; SUCRAFATE; GEMTESA; FINASTERIDE; VITAMIN C [ASCORBIC ACID]; VITAMIN D [VITAMIN D NOS]; B12 [CYANOCOBALAMIN]
Allergien
-
Vorherige Impfungen
-

VAERS 2303473

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
30,0
Geschlecht
M
Eingang
31.05.2022
Impfdatum
24.01.2022
Beginn
24.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Inappropriate schedule of product administration

Symptomtext

Individual received a booster dose on 1/24. Second Pfizer shot was received on 10/7/21. did not catch the mistake that this shot was 2 months early.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2278989

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
65,0
Geschlecht
F
Eingang
16.05.2022
Impfdatum
03.08.2021
Beginn
09.08.2021
Tage bis Beginn
6,0
Dosis
3
Route/Site
SYR / AR
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: unbekannt Erholt: nein
Atrial fibrillation

Symptomtext

I went into A- Fib with both Moderna with booster Pfizer.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Atrial fibrillation
Hospital-Tage
1,0
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Sotalol, amlodipine, magnesium oxide, D3, Prenatal vitamins
Allergien
Penicillin
Vorherige Impfungen
66/went into A-Fib on 2/20/2022 after 02/15/2022 Booster Pfizer

VAERS 2278840

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
13,0
Geschlecht
M
Eingang
16.05.2022
Impfdatum
16.05.2022
Beginn
16.05.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered

Symptomtext

GRANDMOTHER MADE APPOINTMENT FOR GRANDSON BOOSTER; PRESENTED TO SITE WITH CDC CARD FOR BOOSTER; STAFF REVIEWED ALL QUESTIONS AND PROVIDED BOOSTER; WHILE PLACING LABEL OF BOOSTER ON CDC CARD NOTED BOOSTER HAD BEEN GIVEN 1/11/2022 THAT WAS LABELD ON BACK OF CARD THEREFORE THIS WAS A 4TH DOSE OF VACCINE

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
UNK
Vorgeschichte
UNK
Andere Medikamente
UNK
Allergien
UNK
Vorherige Impfungen
-

VAERS 2275900

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
OR
Alter
65,0
Geschlecht
F
Eingang
13.05.2022
Impfdatum
12.10.2021
Beginn
01.12.2021
Tage bis Beginn
50,0
Dosis
4
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Alopecia Blood test abnormal Iron deficiency Iron deficiency anaemia Muscle spasms

Symptomtext

Starting in December of 2021, I developed calf cramps at night. Starting in February of 2022, I had "wads" of hair falling out. I went for a regular exam at the end of march and she ran regular tests. My blood test showed I am iron deficient and I am now taking iron supplements. My hair is no longer falling out as much and I am still having foot cramps at night.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Alopecia
Hospital-Tage
-
Labordaten
Blood tests: iron-deficient anemia
Aktuelle Erkrankungen
None
Vorgeschichte
High cholesterol
Andere Medikamente
Atorvastatin, Fish Oil, Vitamin D, Calcium, Vitamin B , Vitamin E, CoQ10 and Multivitamin
Allergien
TYLOX; shellfish
Vorherige Impfungen
-

VAERS 2268749

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
54,0
Geschlecht
F
Eingang
10.05.2022
Impfdatum
09.04.2022
Beginn
15.04.2022
Tage bis Beginn
6,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blood test Gallbladder polyp Hepatic enzyme increased Hepatic steatosis Respiratory disorder Sputum culture Ultrasound abdomen abnormal Upper respiratory tract infection bacterial

Symptomtext

4/15 I went to ER with upper respiratory issues. Was diagnosed with bacterial upper respiratory infection. During the ER visit elevated liver enzymes were and I was referred to my PCP. PCP has noticed an upward trend in liver enzymes and ordered an ultrasound. Ultrasound report indicated a polyp on gall bladder and fatty liver. PCP referred me to gastroenterologist and I am currently awaiting that appointment.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Blood test
Hospital-Tage
-
Labordaten
Blood work Sputum culture Ultrasound
Aktuelle Erkrankungen
No
Vorgeschichte
None
Andere Medikamente
Montelukast Pantoprazole Famotidine Crestor Multivitamin Ondansetron
Allergien
Erythromycin Simvastatin Morphine Codeine
Vorherige Impfungen
-

VAERS 2267668

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
34,0
Geschlecht
F
Eingang
09.05.2022
Impfdatum
12.02.2022
Beginn
13.02.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Blood immunoglobulin G increased CSF oligoclonal band present Intervertebral disc disorder Lumbar puncture abnormal Lymphadenopathy Magnetic resonance imaging spinal abnormal Myelitis transverse Pleocytosis

Symptomtext

The patient developed L axillary lymphadenopathy on the day after vaccination. Ten days later, she was hospitalized for cervical transverse myelitis, from which she is slowly recovering.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Blood immunoglobulin G increased
Hospital-Tage
5,0
Labordaten
MRI cervical spine 03/01/2022 showed a T2 hyperintense lesion with contrast enhancement from C1 to C3 with associated expansion of the spinal cord. Lumbar puncture 03/01/2022 demonstrated lymphocytic pleocytosis, elevated IgG index and unmatched oligoclonal bands. Extensive evaluation of her blood and spinal fluid did not identify any other provoking factors or underlying medical diagnoses to explain her transverse myelitis.
Aktuelle Erkrankungen
-
Vorgeschichte
migraine
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2267014

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
27,0
Geschlecht
F
Eingang
07.05.2022
Impfdatum
03.04.2022
Beginn
03.04.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered

Symptomtext

This mishap was my fault because, I was not clear on the JJ part. After I gave the okay, I did check with the clinical staff and was told it had to be both series of JJ. I misread the Algorithm for the additional booster. Going for I will be sure the check first with clinical team if I am unsure. Received 1st dose of JJ vaccine May10 /21 and a Pfizer booster on July 6 21 at a pharmacy. Patient states she's here for additional booster as recommended. Discussed with Nurse Evaluator and DOH supervisor on site. Clearance given for patient to receive additional booster.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2258459

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
FL
Alter
72,0
Geschlecht
F
Eingang
29.04.2022
Impfdatum
16.03.2022
Beginn
17.04.2022
Tage bis Beginn
32,0
Dosis
4
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Conjunctivitis Cough Gastrooesophageal reflux disease Productive cough Secretion discharge

Symptomtext

On 04/17/2022 I started getting a cough that I thought was from stopping medication and was Acid reflux. It got worse and started to cough up yellow mucous. It does not go away and I have had dry cough for years but this one is productive with yellow mucous and has not gone away. I still have mucous but it is clear. I also have also had conjunctivitis. I was prescribed Ciprofloxacin eye drops.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Conjunctivitis
Hospital-Tage
-
Labordaten
None.
Aktuelle Erkrankungen
None
Vorgeschichte
Cough
Andere Medikamente
Doxycycline-100mg, Hydromet Cough Syrup PRN 5mil, Welchol 625 milligram once a day at night, Loperamide Hydrochloride - 2 milligrams, and Atorvastatin 20mg.
Allergien
None
Vorherige Impfungen
-

VAERS 2258388

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NJ
Alter
30,0
Geschlecht
F
Eingang
29.04.2022
Impfdatum
14.02.2022
Beginn
19.03.2022
Tage bis Beginn
33,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Abortion spontaneous Exposure during pregnancy

Symptomtext

Miscarriage

Weitere VAERSDATA-Felder
Praegender Schweregrund
Abortion spontaneous
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
Miscarriage on 3/19/2022
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
Miscarriage 3/19/2022.

VAERS 2252220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
38,0
Geschlecht
F
Eingang
26.04.2022
Impfdatum
04.04.2022
Beginn
05.04.2022
Tage bis Beginn
1,0
Dosis
4
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Erythema Skin weeping Swelling

Symptomtext

The next day after the shot I took the Band-Aid off and it was red and raising up and oozing so I put steroid cream on it and it took 3 days to dry it out.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Erythema
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Hashimoto's; Auto immune thyroiditis; Uri cardio; Migraines; Galactorrhea; Thyroid nodule; Cervical Dysplasia
Andere Medikamente
Botox injections; Depo-Provera; Topiramate 100mg; Trimoxicillin 30mcg; Adapalene 0.3 mg; Nasal Spray; Allegra; Levothyroxine 88 mcg; Vitamin D 2000 units; Valacyclovir; Duloxetine 60mg; Ferrous Gluconate; Cyclosporine; Montelukast; Doxycycl
Allergien
Penicillin; Latex; Lamotrigine; Depakote
Vorherige Impfungen
-

VAERS 2248362

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
30,0
Geschlecht
F
Eingang
22.04.2022
Impfdatum
01.01.2022
Beginn
03.04.2022
Tage bis Beginn
92,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
COVID-19 Vaccine breakthrough infection

Symptomtext

Breakthrough case of COVID 19

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
-
Andere Medikamente
-
Allergien
clyndamyacin/mynocycline
Vorherige Impfungen
-

VAERS 2247842

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
FL
Alter
64,0
Geschlecht
F
Eingang
22.04.2022
Impfdatum
01.04.2022
Beginn
04.04.2022
Tage bis Beginn
3,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Laryngitis SARS-CoV-2 test negative Tonsillar hypertrophy

Symptomtext

Developed laryngitis and enlarged tonsils for 7 seven days.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Laryngitis
Hospital-Tage
-
Labordaten
COVID test at home negative twice
Aktuelle Erkrankungen
no
Vorgeschichte
Hypertension
Andere Medikamente
Prempro Benicar Rovastatin Metoprolol MVI Calcium Curcumin Probiotic Vitamin D Vitamin C
Allergien
PCN
Vorherige Impfungen
-

VAERS 2241117

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
VA
Alter
66,0
Geschlecht
M
Eingang
19.04.2022
Impfdatum
07.04.2022
Beginn
10.04.2022
Tage bis Beginn
3,0
Dosis
4
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Lip swelling Oral herpes

Symptomtext

A few days after the vaccine I woke and I could feel that I had a cold sore on my lip. When I got to the mirror to look at it I realized it was swollen up to be the size of about golf ball or lemon. I went to the doctor but before I had gotten appointment I was using an OTC medication and the swelling was going down at that point so we did not treat it further.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Lip swelling
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
COPD; Recovering from lung cancer
Andere Medikamente
Psilocin ACL, Low dose Aspirin, Trilogy inhaler, Guaifenesin , Digest-well, Lapia enzyme complex, Probiotic multienzyme, multivitamin, Cyclobenzaprine Metoclopramide, Oxycodone, Simethicone, Diphenhydramine Ibuprofen Nyquil
Allergien
None
Vorherige Impfungen
-

VAERS 2236193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
39,0
Geschlecht
F
Eingang
15.04.2022
Impfdatum
15.04.2022
Beginn
15.04.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered Interchange of vaccine products

Symptomtext

CLIENT HAD INITIAL SERIES OF 1 JANSSEN COVID VACCINE 3/6/2021; BOOSTER MODERNA GIVEN 11/3/2021; PROVIDED ADDITIONAL BOOSTER PFIZER DOSE TODAY 4/15/2022; CLIENT NOT IMMUNOCOMPROMISED OR OVER AGE 50 YRS THEREFORE DID NOT MEET ADDITINAL DOSE CRITERIA ; NO SIDE EFFECTS AND RELEASED TO HER OWN CARE.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
NONE
Aktuelle Erkrankungen
unk
Vorgeschichte
unk
Andere Medikamente
unk
Allergien
unk
Vorherige Impfungen
-

VAERS 2216011

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
63,0
Geschlecht
M
Eingang
05.04.2022
Impfdatum
23.02.2022
Beginn
16.03.2022
Tage bis Beginn
21,0
Dosis
3
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt
Bladder mass

Symptomtext

Currently (4/5/2022) admitted to hospice for a bladder tumor. Hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Bladder mass
Hospital-Tage
20,0
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2209990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
VA
Alter
75,0
Geschlecht
M
Eingang
31.03.2022
Impfdatum
31.03.2022
Beginn
-
Tage bis Beginn
-
Dosis
4
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered

Symptomtext

Patient received primary series of Sinopharm 5/11/21, 2nd dose Sinopharm on 6/6/21. Patient also received a booster dose of Sinopharm on 11/24/21. Therefore, the patient should not have received a second booster dose.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
N/A
Vorgeschichte
H/O MI 2007
Andere Medikamente
N/A
Allergien
n/a
Vorherige Impfungen
-

VAERS 2209087

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
62,0
Geschlecht
M
Eingang
31.03.2022
Impfdatum
29.03.2022
Beginn
09.03.2022
Tage bis Beginn
-
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered Interchange of vaccine products

Symptomtext

A participant presented at clinic requesting to get a first dose of Pfizer and was registered on site. After the participant received the Pfizer vaccination, upon review of his appointment in the Database, it was discovered that he had received 9 doses of Pfizer and 1 dose of JNJ at the clinic. A check verified database information and an additional 4 doses of JNJ and 1 Moderna outside of clinic was also identified as well as 2 influenza vaccines. The participant denied receiving multiple doses of vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2196478

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PA
Alter
59,0
Geschlecht
F
Eingang
24.03.2022
Impfdatum
10.01.2022
Beginn
12.01.2022
Tage bis Beginn
2,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Nasal congestion Respiratory tract congestion Rhinorrhoea Secretion discharge Sneezing

Symptomtext

Sneezing, runny nose, congestion. Within approximately 4-5 day, mucus in nose became congestive and stringy when blowing nose. As of today 3/24/2022, it is still that way.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Nasal congestion
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Sarcoidosis
Vorgeschichte
Sarcoidosis
Andere Medikamente
Multivitamin, fish oil, vitamin D, magnesium
Allergien
Clindamycin, ciprofloxacin, epinephrine, xanax, metoprolol
Vorherige Impfungen
-

VAERS 2187550

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge FJ5683

gering
Staat
KY
Alter
43,0
Geschlecht
F
Eingang
18.03.2022
Impfdatum
15.03.2022
Beginn
17.03.2022
Tage bis Beginn
2,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Heavy menstrual bleeding Vaginal haemorrhage

Symptomtext

Vaginal bleeding after both first and second shot. I have never had off cycle bleeding in my entire life and I am 43. The bleeding is not a small amount of blood and alarming.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Heavy menstrual bleeding
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
-
Vorherige Impfungen
Yes swelling of eyes but never bleeding

VAERS 2184166

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
48,0
Geschlecht
M
Eingang
17.03.2022
Impfdatum
25.02.2022
Beginn
28.02.2022
Tage bis Beginn
3,0
Dosis
UNK
Route/Site
SYR / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Tinnitus

Symptomtext

High frequency ringing sound in both ears 24/7 throughout the day. Have not consulted a physician yet.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Tinnitus
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2177360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj5683

gering
Staat
IN
Alter
52,0
Geschlecht
F
Eingang
13.03.2022
Impfdatum
11.03.2022
Beginn
11.03.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Aphthous ulcer

Symptomtext

Inside top left cheek. ?Splattering? of canker soars.maybe 8-10. Fully disappeared by sunday morning /about 48 hours after shot. I took more l-lysine. When i had the outbreak but nothing else

Weitere VAERSDATA-Felder
Praegender Schweregrund
Aphthous ulcer
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Nope
Vorgeschichte
-
Andere Medikamente
Chlorophyll L-lysine - just started androgel testosterone 2 weeks ago 2x a week maybe 5mg
Allergien
No
Vorherige Impfungen
03/11/2022

VAERS 2165530

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CO
Alter
11,0
Geschlecht
M
Eingang
08.03.2022
Impfdatum
19.01.2022
Beginn
08.03.2022
Tage bis Beginn
48,0
Dosis
1
Route/Site
IM / RL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
No adverse event

Symptomtext

No adverse event occurred. MA pulled this dosage in error and was given to patient.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2161929

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
19,0
Geschlecht
F
Eingang
05.03.2022
Impfdatum
28.02.2022
Beginn
28.02.2002
Tage bis Beginn
-
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Inappropriate schedule of product administration

Symptomtext

The vaccinator used a booster calendar to verify patient was within the timeframe to receive the Pfizer booster shoot. Because the patient received the second dose on 09/29/2021, the system would not let the vaccinator proceed with the shot. The booster calendar stated the patient could receive the shot on 02/28/2022, so I move the 2nd date of the Pfizer vaccine to 09/28/2021 thinking I would be able to go back afterwards and correct the date. I was unable to correct my error. I noted the account of the actual Pfizer 2nd dose date of 09/29/2021.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
None.
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2161901

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
SC
Alter
36,0
Geschlecht
F
Eingang
05.03.2022
Impfdatum
03.02.2022
Beginn
10.02.2022
Tage bis Beginn
7,0
Dosis
1
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Blindness Iritis Uveitis

Symptomtext

7 days, post 1st dose, developed uveitis (iritis) in left eye. Loss of vision in left eye for 2 weeks, with oral and topical steroids. Still unable to see clearly out of left eye.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Blindness
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2151561

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
KY
Alter
34,0
Geschlecht
F
Eingang
02.03.2022
Impfdatum
21.01.2022
Beginn
25.01.2022
Tage bis Beginn
4,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
COVID-19 SARS-CoV-2 test positive

Symptomtext

Tested Positive for Covid

Weitere VAERSDATA-Felder
Praegender Schweregrund
COVID-19
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2151466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
38,0
Geschlecht
F
Eingang
01.03.2022
Impfdatum
14.01.2022
Beginn
24.01.2022
Tage bis Beginn
10,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: ja ER: unbekannt Erholt: nein
Acne Blood culture negative Blood test abnormal Computerised tomogram abdomen normal Computerised tomogram kidney normal Contusion Haemorrhage Heavy menstrual bleeding Petechiae Platelet count decreased Platelet transfusion SARS-CoV-2 test

Symptomtext

After shot within the week I started my period, but it was unusually heavy. Pimples that I picked kept bleeding. 1/27 got up around 6:30am took shower and noticed large bruised on leg and lower back and hip and various places. Also noticed little petechiae. I called the doctor. 1/28 went and did blood test-platelets in blood decrease excessively. I went to the hospital ER 1/29. Did CT scan- no bleeding. Did a platelet transfusion and still continued to drop. I was admitted about 9pm and saw doctor next morning. I was hospitalized for 4 days and was prescribed dexamethasone for two days then prednisone.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Acne
Hospital-Tage
4,0
Labordaten
Platelet Transfusion- Platelets continued to drop; blood test; covid test; blood culture- normal; CT scan- of abdomen and kidney- normal.
Aktuelle Erkrankungen
No
Vorgeschichte
Microscopic colitis
Andere Medikamente
No
Allergien
Latex and some adhesive
Vorherige Impfungen
-

VAERS 2194064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
75,0
Geschlecht
M
Eingang
24.02.2022
Impfdatum
18.01.2022
Beginn
18.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein
Unevaluable event

Symptomtext

Narrative:

Weitere VAERSDATA-Felder
Praegender Schweregrund
Unevaluable event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2135341

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
MN
Alter
11,0
Geschlecht
M
Eingang
23.02.2022
Impfdatum
22.02.2022
Beginn
22.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered

Symptomtext

Pfizer 12+ was accidentally administered to this 11yo who should have received Pfizer 5-11yo.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
NA
Vorgeschichte
NA
Andere Medikamente
NA
Allergien
NA
Vorherige Impfungen
-

VAERS 2135340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
MN
Alter
8,0
Geschlecht
M
Eingang
23.02.2022
Impfdatum
22.02.2022
Beginn
22.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered

Symptomtext

Pfizer 12+ was accidentally administered to this 8yo who should have received Pfizer 5-11yo.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
NA
Vorgeschichte
NA
Andere Medikamente
NA
Allergien
NA
Vorherige Impfungen
-

VAERS 2134656

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CO
Alter
11,0
Geschlecht
M
Eingang
23.02.2022
Impfdatum
06.01.2022
Beginn
06.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Incorrect dose administered No adverse event

Symptomtext

Patient was given the 12 and older vaccine 0.3 ML, no known symptoms or problems

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
Bicillin
Vorherige Impfungen
-

VAERS 2134479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NC
Alter
67,0
Geschlecht
M
Eingang
23.02.2022
Impfdatum
18.02.2022
Beginn
19.02.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Vertigo

Symptomtext

Severe vertigo; lasted approximately 5-6 hours. Slept and the next am it was resolved. Vertigo when head elevated; when lying down with eyes closed it was less impactful.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Vertigo
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
Migraine
Andere Medikamente
Imitrex as needed--not taken that day; flexeril 20mg daily
Allergien
NKA
Vorherige Impfungen
-

VAERS 2131289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
IL
Alter
14,0
Geschlecht
F
Eingang
22.02.2022
Impfdatum
22.02.2022
Beginn
22.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Underdose

Symptomtext

Patient received adult dose of Pfizer on 1-29-2022 (0.3 mg) then received Pfizer Pediatric Dose on 2-19-2022.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Underdose
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
unknown
Vorgeschichte
unknown
Andere Medikamente
unknown
Allergien
unknown
Vorherige Impfungen
-

VAERS 2128563

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fJ5683

gering
Staat
RI
Alter
11,0
Geschlecht
M
Eingang
20.02.2022
Impfdatum
20.02.2022
Beginn
20.02.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered No adverse event

Symptomtext

Patient received Pfizer adult dose (12+ y.o.) when he should have received Pfizer pediatric dose (5-11y.o.). No adverse reaction was observed.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2123930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
IA
Alter
13,0
Geschlecht
F
Eingang
18.02.2022
Impfdatum
14.02.2022
Beginn
16.02.2022
Tage bis Beginn
2,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Aphthous ulcer

Symptomtext

Lipschutz Ulcer or Vulvar Aphthous Ulcer VIRUS.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Aphthous ulcer
Hospital-Tage
-
Labordaten
Medical exam of 13 year old not sexually active girl.
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
tree nut allergy
Vorherige Impfungen
-

VAERS 2123381

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PA
Alter
19,0
Geschlecht
M
Eingang
18.02.2022
Impfdatum
10.02.2022
Beginn
10.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Asthenia Hyperhidrosis Pallor

Symptomtext

pt became diaphoretic, weak, and pale. BP 88/56, Pulse 84, O2 95%. On reassessment a few minutes later, BP 108/80, Pulse 77, O2 99%. pt was checked by physician who determined he was allowed to leave.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Asthenia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
n/a
Vorgeschichte
-
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2119694

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

gering
Staat
NV
Alter
59,0
Geschlecht
M
Eingang
17.02.2022
Impfdatum
18.01.2022
Beginn
02.02.2022
Tage bis Beginn
15,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Hypoaesthesia

Symptomtext

numbness in hand

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypoaesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
losartan, metformin,
Allergien
-
Vorherige Impfungen
-

VAERS 2116112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PR
Alter
35,0
Geschlecht
F
Eingang
16.02.2022
Impfdatum
13.01.2022
Beginn
13.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Discomfort Feeling cold Hypoaesthesia

Symptomtext

The patient explains to the nurse that the previous time her BP went up and the Lt presented hemiparesis, she went to the hospital and had PTB. Received TX and resolved after the BP patient is vaccinated in area. Approx. 10 min patient reports that he begins to feel numbness in the chest and arm L side, patient has PMS in extremity, feels cold, pulse movement and sensation in extremity. Evaluated patient is left under monitoring patient does not want to go to hospital and wants to leave patient was oriented.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Discomfort
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
Vitamin C, Vitamin D.
Allergien
Acetaminophen, Sulfa, Aloe.
Vorherige Impfungen
Yes. Raised BP

VAERS 2116043

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
60,0
Geschlecht
M
Eingang
16.02.2022
Impfdatum
09.01.2022
Beginn
10.01.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Facial asymmetry Oedema peripheral

Symptomtext

Patient presented to vaccine site for second Pfizer vaccine. Patient conveys that he developed facial edema and lower extremity edema approximately 24 hours post Pfizer vaccine. He did not seek medical care. The symptoms resolved over the course of the week. No respiratory issues.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Facial asymmetry
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Unknown
Andere Medikamente
Unknown
Allergien
NKA
Vorherige Impfungen
-

VAERS 2110479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PA
Alter
47,0
Geschlecht
F
Eingang
14.02.2022
Impfdatum
14.02.2022
Beginn
14.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Epistaxis

Symptomtext

Felt my nose dripping when I got in the car and tissue had blood so I pinched it until I got home. It?s now 6 hours later and still dripping blood.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Epistaxis
Hospital-Tage
-
Labordaten
NA
Aktuelle Erkrankungen
Positive covid test 1/24/22
Vorgeschichte
Ankylosing spondylitis Cataracts Glaucoma ADHD Hyper mobility Vitamin d deficiency Gallbladder out in 1994
Andere Medikamente
Adderall xr 10 mg Celexa 10 mg
Allergien
Sulfa drugs Seafood
Vorherige Impfungen
-

VAERS 2110109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
MN
Alter
33,0
Geschlecht
F
Eingang
14.02.2022
Impfdatum
12.02.2022
Beginn
12.02.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Inappropriate schedule of product administration

Symptomtext

Second dose was given too early.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2108890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
-
Geschlecht
F
Eingang
12.02.2022
Impfdatum
21.01.2022
Beginn
21.01.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Dysphagia Hypersensitivity Hypoaesthesia oral Throat tightness

Symptomtext

allergic reaction; lips started to get numb; throat feels like closing up; hard to swallow; This is a spontaneous report received from a non-contactable reporter (Consumer or other non-HCP) from medical information team for a Pfizer sponsored program (159558). The reporter is the patient. AA female patient received bnt162b2 (BNT162B2), administration date 21Jan2022 (Lot number: FJ5683, Expiration Date: 31Jan2022) as dose number unknown (booster), single for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: BENADRYL taken for premedication, start date: 21Jan2022. Vaccination history included: Covid-19 vaccine (Primary Immunization completed but manufacturer unknown), for Covid-19 immunization. The following information was reported: HYPERSENSITIVITY (medically significant) with onset 21Jan2022, outcome "unknown", described as "allergic reaction"; HYPOAESTHESIA ORAL (medically significant) with onset 21Jan2022, outcome "unknown", described as "lips started to get numb"; THROAT TIGHTNESS (medically significant) with onset 21Jan2022, outcome "unknown", described as "throat feels like closing up"; DYSPHAGIA (medically significant) with onset 21Jan2022, outcome "unknown", described as "hard to swallow". The events "allergic reaction", "lips started to get numb", "throat feels like closing up" and "hard to swallow" were evaluated at the emergency room visit. Therapeutic measures were taken as a result of throat tightness. Clinical course was as follows: The patient reported after getting her booster shot on 21Jan2022, she ended up having allergic reaction to it and she spent 2 and half hours in the urgent care. Patient stated that her lips started to get numb and her throat feels like closing up and it's hard to swallow. Patient also stated that prior to getting the booster shot, they gave her Benadryl, it wasn't liquid, it was a pill. 30 minutes prior to getting the shot, but it didn't help and gave her a breathing treatment. She experienced the adverse reaction within 2 minutes or so. Patient also stated that other people are telling her that their tongues are getting numb, and per patient she wants to report it. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Dysphagia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
BENADRYL
Allergien
-
Vorherige Impfungen
-

VAERS 2201162

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
62,0
Geschlecht
F
Eingang
11.02.2022
Impfdatum
10.01.2022
Beginn
27.12.2021
Tage bis Beginn
-
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Asthenia COVID-19 Chest X-ray normal Cough Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Narrative: COVID infection following COVID vaccine series 02/04, Pfizer dose #1 02/25, Pfizer, dose #2 1/10, Pfizer, dose #2 12/28 COVID swab, result: detected 12/20 COVID swab, result: not detected 12/30 COVID swab, result: detected 1/5 COVID swab, result: detected 12/27 pt cc: cough/congestion and weakness exposure: unknown 12/30 pt admit ED cc: cough/congestion and weakness dx: COVID LOS: 1 day 12/30 CXR impression: No acute abnormality.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Asthenia
Hospital-Tage
-
Labordaten
12/28 COVID swab, result: detected 12/20 COVID swab, result: not detected 12/30 COVID swab, result: detected 1/5 COVID swab, result: detected 12/30 CXR impression, No acute abnormality.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2101709

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PR
Alter
55,0
Geschlecht
M
Eingang
10.02.2022
Impfdatum
18.01.2022
Beginn
18.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Aphasia Dysphonia Lip swelling

Symptomtext

Patient reports feeling swollen lips, hoarseness and trouble speaking.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Aphasia
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
n/a
Vorherige Impfungen
-

VAERS 2092695

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
45,0
Geschlecht
F
Eingang
07.02.2022
Impfdatum
02.02.2022
Beginn
02.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Inappropriate schedule of product administration

Symptomtext

Pt received booster less than 5 months apart

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2091683

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PR
Alter
25,0
Geschlecht
F
Eingang
05.02.2022
Impfdatum
13.01.2022
Beginn
20.01.2022
Tage bis Beginn
7,0
Dosis
UNK
Route/Site
- / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Eye irritation Laboratory test normal Sensitive skin

Symptomtext

Sensitivity in the skin, irritation in the right eye, doctors did not find and infection and with treatment it has not improved.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Eye irritation
Hospital-Tage
-
Labordaten
Cavernous sinus thrombosis negative, Conjunctivitis negative
Aktuelle Erkrankungen
Covid-19; Hypoglycemia; Chronic sinusitis
Vorgeschichte
-
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2091630

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
26,0
Geschlecht
M
Eingang
05.02.2022
Impfdatum
05.02.2022
Beginn
05.02.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Hyperhidrosis Pallor

Symptomtext

About 13:50, patient came to observation. I noticed patient sitting in chair with mask off. When nurse went over to patient to request for him to put mask on, she noticed he was pale and diaphoretic. Nurse brought juice and water. He felt better but continued to appear pale and diaphoretic. 13:55: Placed pulse oximeter on patient: 97% o2; 109 pulse. 13:59: Assisted patient to cot to lay down with feet elevated. Vital taken: 130/86; 98% o2; pulse 83. Patient felt better and color was improving. 14:15 - Assisted patient to sitting on cot. Vitals taken: 132/84; 99% o2; 88 HR; 18 R. 14:30- Assisted patient to stand. Vitals taken: 138/90; 98 % o2; 98 HR; 12 R. Returned patient to chair. Patient continued to improve in color and stated feeling better. BP in chair 14:44: 127/86. Patient left without assistant at 14:45 with his friend.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hyperhidrosis
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2088077

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
KS
Alter
44,0
Geschlecht
F
Eingang
04.02.2022
Impfdatum
04.02.2022
Beginn
04.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Inappropriate schedule of product administration

Symptomtext

Patient presented at a Covid-19 vaccine event at local store this morning requesting a Pfizer booster. She filled out appropriate paperwork and there were no contraindications noted. Only after patient left and I was reviewing paperwork did I notice the dates of her initial doses of 09/01/2021 and 10/31/2021 and I had given her booster dose sooner than 5 months from completing her primary series. She was still at the facility, so I called patient to come back to the room at 0655. She returned at 0840. I explained that she had received the booster too early and while there is no danger to her I encouraged her to stay aware of any adverse reactions. She said she understood and returned to work.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2088046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
80,0
Geschlecht
M
Eingang
04.02.2022
Impfdatum
19.01.2022
Beginn
19.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Peripheral swelling Skin warm

Symptomtext

On 01/25/2022 patient walked in while we were having the COVID clinic and stated that he had his Pfizer booster on 1/19/2022 at about noon and by 3 O'clock that after noon his left hand had swelled up and warm to the touch. Patient stated that he got his vaccine in the left deltoid. No other symptoms noted. He just wanted us to know.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Peripheral swelling
Hospital-Tage
-
Labordaten
NONE
Aktuelle Erkrankungen
none
Vorgeschichte
depression, sleep apnea, chronic back pain, HTN, DM, hyperlipidemia, hearing loss,
Andere Medikamente
Rosuvastatin, Amlodipine Besylate, Cyanoccobalamin, Monetasone Actuat Oral inhaler, Clopidogrel Bisulfate, Metformin, Apixaban, Lidocaine oint, Menthol/M-Salicylate top cream, Levothyroxine Na, Albuterol oral inhaler, Lisinopril, Hydrochlo
Allergien
Sertraline and Fluticasone/Salmeterol
Vorherige Impfungen
-

VAERS 2087744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
WA
Alter
12,0
Geschlecht
F
Eingang
04.02.2022
Impfdatum
19.06.2021
Beginn
19.07.2021
Tage bis Beginn
30,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Amenorrhoea

Symptomtext

Patient has not had a menstrual cycle since receiving her second dose of the vaccine. No periods, and she had been experiencing regular cycles since she turned 11.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Amenorrhoea
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
Amoxicillin
Vorherige Impfungen
-

VAERS 2085628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
55,0
Geschlecht
F
Eingang
03.02.2022
Impfdatum
03.02.2022
Beginn
03.02.2022
Tage bis Beginn
0,0
Dosis
4
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered Interchange of vaccine products

Symptomtext

None, patient was physically fine and expressed no pain or discomfort after vaccination. Patient was accidentally given a second Pfizer booster when it should have been a Flu vaccine. Patient was informed of the misdose and then still consented and received the Flu vaccine in the same arm, per request, after the Pfizer dose.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2085156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PA
Alter
15,0
Geschlecht
M
Eingang
03.02.2022
Impfdatum
10.01.2022
Beginn
10.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered

Symptomtext

Patient received the pediatric formulation instead of the teenage/adult formulation. This 15 year old received 10 mcg of mRNA Pfizer instead of the recommended 30 mcg mRNA Pfizer for 12 and over.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2079602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
18,0
Geschlecht
F
Eingang
01.02.2022
Impfdatum
01.02.2022
Beginn
01.02.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Inappropriate schedule of product administration

Symptomtext

2/1/2022 18-year-old female received booster shy of 5-month CDC guideline recommendation. EMT-C16023 miscalculated date and administered booster 14 days before due date.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
NKI
Vorgeschichte
NONE
Andere Medikamente
NA
Allergien
NKA
Vorherige Impfungen
-

VAERS 2079520

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
11,0
Geschlecht
F
Eingang
01.02.2022
Impfdatum
01.02.2022
Beginn
01.02.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered No adverse event

Symptomtext

Patient received adult Pfizer vaccine when she should have received the pediatric dose (patient is 11 years old). No adverse reaction was observed and no treatment was required.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
Unknown
Vorgeschichte
Developmental delayed
Andere Medikamente
Unknown
Allergien
None stated
Vorherige Impfungen
-

VAERS 2075601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

gering
Staat
OH
Alter
34,0
Geschlecht
F
Eingang
31.01.2022
Impfdatum
29.01.2022
Beginn
29.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / OT
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Extra dose administered No adverse event Product administration error

Symptomtext

Patient intended to receive 1 dose of flu shot and booster pfizer dose. The pharmacist administered 2 doses of pfizer by mistake. A shot was given in each deltoid on 1/29/2022. Patient was immediately made aware. Pt followed up with on call PCP and was told to monitor symptoms. Pharmacy followed up with patient's PCP on 1/31/2022 (office was closed during weekend). Pharmacist followed up with Drug Info specialist hotline 1/31/2022 (office closed during weekend). Patient had not experienced any adverse reaction on 1/29/2022 and not reported any reaction to Pharmacy as of 1/31/2022. Patient was advised to monitor symptoms and seek emergency help if any symptoms arise.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2073064

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
31,0
Geschlecht
M
Eingang
28.01.2022
Impfdatum
10.01.2022
Beginn
10.01.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Hypoaesthesia Lymphadenopathy

Symptomtext

Lymph node swelling in axilla. Numbness in stocking distribution to arms and legs bilaterally.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypoaesthesia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2072488

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
FL
Alter
27,0
Geschlecht
M
Eingang
28.01.2022
Impfdatum
28.01.2022
Beginn
28.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Retching

Symptomtext

With 1 or 2 minutes of getting vaccine patient started dry heaving. Patient had no signs of allergic reaction, no swelling or difficulty breathing. After giving a patient to feel better and not feeling better ambulance was called. EMS stated all vitals and breathing were good. Patient wanted to go to hospital and EMS took patient to the hospital.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Retching
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
food
Vorherige Impfungen
Patient stated that vomited immediately after first dose but felt better in 10 minutes. Was very nervous.

VAERS 2072192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
VT
Alter
10,0
Geschlecht
M
Eingang
28.01.2022
Impfdatum
28.01.2022
Beginn
28.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered

Symptomtext

Patient received adult dose of 0.3ml and adult vial.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
n/a
Vorherige Impfungen
-

VAERS 2072142

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
20,0
Geschlecht
M
Eingang
28.01.2022
Impfdatum
28.01.2022
Beginn
28.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Wrong technique in product usage process

Symptomtext

Patient received first dose of Pfizer COVID-19 vaccine at a different site 21 days ago and received 2nd dose of series today. After receiving his vaccination, he stated he received 2 doses of Sinovac a "long time ago." Patient aware that he was vaccinated against CDC guidelines, since he already received a WHO-approved COVID-19 vaccine.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong technique in product usage process
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2071808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
23,0
Geschlecht
F
Eingang
28.01.2022
Impfdatum
28.01.2022
Beginn
28.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Chest discomfort Erythema Feeling hot

Symptomtext

Note: Dose 1 and 2 patient had Moderna. Reaction occurred to Pfizer booster (3rd shot). Redness on arms/chest, tightness in the chest and felt hot. Reaction only lasted 30 seconds to a minute. Patient could speak the entire time. EpiPen not needed as reaction subsided. Patient felt fine when EMS arrived but went to the hospital as a precaution to be checked-out.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Chest discomfort
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
Asthma
Andere Medikamente
N/A
Allergien
Penicillin
Vorherige Impfungen
-

VAERS 2071741

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
9,0
Geschlecht
M
Eingang
28.01.2022
Impfdatum
27.01.2022
Beginn
27.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered

Symptomtext

9-year-old patient received an adult dose of Pfizer vaccine for their 2nd dose in COVID-19 vaccine series.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
N/A
Allergien
None
Vorherige Impfungen
-

VAERS 2070017

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
18,0
Geschlecht
F
Eingang
27.01.2022
Impfdatum
27.01.2022
Beginn
27.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Inappropriate schedule of product administration

Symptomtext

Patient had registered on the computer for the booster vaccine, checked off the box that stated she had received her 2nd dose at least 5 months prior. After the Booster was given she then informed our PA that it had been 3-4 months since last Covid vaccine. Patient tolerated vaccine well, reported no symptoms.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2069114

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
85,0
Geschlecht
F
Eingang
27.01.2022
Impfdatum
26.01.2022
Beginn
27.01.2022
Tage bis Beginn
1,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Product storage error

Symptomtext

Patient was administered with vaccine - post puncture that was exposed to non suitable temperature for over 24 hours.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Product storage error
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2069105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
6,0
Geschlecht
M
Eingang
27.01.2022
Impfdatum
26.01.2022
Beginn
01.01.2022
Tage bis Beginn
-
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Unevaluable event

Symptomtext

N/A

Weitere VAERSDATA-Felder
Praegender Schweregrund
Unevaluable event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2069099

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
6,0
Geschlecht
F
Eingang
27.01.2022
Impfdatum
26.01.2022
Beginn
01.01.2022
Tage bis Beginn
-
Dosis
1
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Unevaluable event

Symptomtext

N/A

Weitere VAERSDATA-Felder
Praegender Schweregrund
Unevaluable event
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2065798

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
VA
Alter
49,0
Geschlecht
M
Eingang
26.01.2022
Impfdatum
15.01.2022
Beginn
15.01.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Inappropriate schedule of product administration

Symptomtext

*1220 - Vaccinator alerted safety officer of vaccine error for client . *Client was given booster today before 150 day eligibility. *Client?s vaccination card labeled 2nd dose ?9/30/21? was written in poor handwriting ? 9 looked like a 4. *Spreadsheet from registration was inputted as 4/30/21. *Previous doses were done outside pharmacy.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
unknown
Allergien
nkda
Vorherige Impfungen
-

VAERS 2647079

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
17,0
Geschlecht
F
Eingang
25.01.2022
Impfdatum
25.01.2022
Beginn
25.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Inappropriate schedule of product administration

Symptomtext

SECOND DOSE GIVEN 12 DAYS EARLY

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2062470

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NY
Alter
76,0
Geschlecht
F
Eingang
25.01.2022
Impfdatum
25.01.2022
Beginn
25.01.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
- / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Wrong technique in product usage process

Symptomtext

Six syringes were discovered to be empty with no vaccine in them. Administrator injected needle into left deltoid and noticed it was empty. Needle was immediately pulled out without injection. Patient allowed a second vaccination. All empty syringes were removed from vaccination area.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Wrong technique in product usage process
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2060309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
5,0
Geschlecht
F
Eingang
24.01.2022
Impfdatum
24.01.2022
Beginn
24.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered No adverse event

Symptomtext

ADULT PFIZER COVID 19 VACCINE WAS INADVERTENTLY ADMINISTERED TO 5 Y.O. PEDIATRIC PATIENT. PATIENT DOES NOT HAVE ANY SIDE EFFECTS AS OF YET

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
-
Andere Medikamente
-
Allergien
no known allergy
Vorherige Impfungen
-

VAERS 2060270

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

gering
Staat
OR
Alter
47,0
Geschlecht
F
Eingang
24.01.2022
Impfdatum
14.01.2022
Beginn
24.01.2022
Tage bis Beginn
10,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Interchange of vaccine products

Symptomtext

pt got first dose moderna, 2nd dose pfizer, and 3rd dose pfizer

Weitere VAERSDATA-Felder
Praegender Schweregrund
Interchange of vaccine products
Hospital-Tage
-
Labordaten
na
Aktuelle Erkrankungen
na
Vorgeschichte
na
Andere Medikamente
na
Allergien
na
Vorherige Impfungen
-

VAERS 2060265

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

gering
Staat
OR
Alter
24,0
Geschlecht
M
Eingang
24.01.2022
Impfdatum
14.01.2022
Beginn
24.01.2022
Tage bis Beginn
10,0
Dosis
2
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Inappropriate schedule of product administration

Symptomtext

Got his first dose on 12/31/2021 and got his second dose on 1/14/2022, one week too soon.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
n/a
Allergien
N/A
Vorherige Impfungen
-

VAERS 2060253

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

gering
Staat
OR
Alter
52,0
Geschlecht
M
Eingang
24.01.2022
Impfdatum
14.01.2022
Beginn
24.01.2022
Tage bis Beginn
10,0
Dosis
2
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Interchange of vaccine products

Symptomtext

Pt got moderna 1st dose and got pfizer the second dose. Not sure why he asked for pfizer second dose

Weitere VAERSDATA-Felder
Praegender Schweregrund
Interchange of vaccine products
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-

VAERS 2054650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
35,0
Geschlecht
F
Eingang
21.01.2022
Impfdatum
11.01.2022
Beginn
11.01.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / -
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Interchange of vaccine products

Symptomtext

11:10 - *Safety Officer called by vaccinator lead to incident with vaccinator. *Client was here for Moderna 2nd dose, was accidentally given Pfizer by vaccinator. *Client was given appropriate identification slips (Moderna, 2nd dose) but assigned to Pfizer table by line flow. *Vaccinator did not verbally confirm vaccine type with client prior to vaccinating. *Vaccinator failed to check prior vaccine logged into system.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Interchange of vaccine products
Hospital-Tage
-
Labordaten
n/a
Aktuelle Erkrankungen
n/a
Vorgeschichte
n/a
Andere Medikamente
n/a
Allergien
n/a
Vorherige Impfungen
-

VAERS 2054601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge fj5683

gering
Staat
-
Alter
45,0
Geschlecht
M
Eingang
21.01.2022
Impfdatum
19.01.2022
Beginn
19.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Device connection issue

Symptomtext

Upon withdrawing, the syringe and the needle were detached. The Needle was removed. Patient notified that he received all the medication.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Device connection issue
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2052280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
15,0
Geschlecht
M
Eingang
20.01.2022
Impfdatum
15.01.2022
Beginn
15.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Apraxia Dysarthria Immediate post-injection reaction Musculoskeletal disorder Visual impairment

Symptomtext

Immediately after the injection of the vaccine, patient eyes started to close and body started to slightly slack. I called out to the patient and roused him. He was able to open his eyes slightly. I asked if he was ok and he answer in a slurred speech. He was able to tell me his name. I remembered that before the injection, he said he didn't like shots and he made a point to look away. I asked if he was holding his breath when I gave him the injection. He said yes. His mother also admitted that he had a fear of shots since he was young but he has never fainted or blacked out. He then said that he could barely see; he also saw black dots. All the while, he could barely keep his eyes open. We kept talking to him to get him talking. His color looked normal to me. We suspected maybe look sugar level since he didn't eat a proper meal and maybe low blood pressure. I took his blood pressure and it was 75/50 mmHg with a HR of 56. Mother did not know his normal BP level since he doesn't regularly visit a doctor. We gave him a candy just in case his sugar level was low. A few minutes later, the patient resumed his normal vision. He was able to keep his eyes open. He was able to stand up and walk.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Apraxia
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
NONE
Vorgeschichte
NONE
Andere Medikamente
-
Allergien
NONE
Vorherige Impfungen
-

VAERS 2051046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
SC
Alter
15,0
Geschlecht
F
Eingang
20.01.2022
Impfdatum
19.01.2022
Beginn
20.01.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Swelling face

Symptomtext

Swelling of the face.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Swelling face
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
Asthma
Andere Medikamente
Dupixent
Allergien
None
Vorherige Impfungen
-

VAERS 2046447

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PR
Alter
33,0
Geschlecht
F
Eingang
19.01.2022
Impfdatum
18.01.2022
Beginn
18.01.2022
Tage bis Beginn
0,0
Dosis
UNK
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Inappropriate schedule of product administration

Symptomtext

Patient arrives at the center to be vaccinated without the vaccination card since she had left it, she agrees to bring it the same day and she assures that 5 months have passed since her second dose. Relative of the patient brings the card in the afternoon to sign it and we realized that the 5 months of his second administration had not yet passed. we proceeded to call the health department, we contacted provider and she indicated to make a report in VAERS and that the president be notified of what happened. The patient is informed and indicates that she is in good health.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2044474

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TN
Alter
35,0
Geschlecht
F
Eingang
18.01.2022
Impfdatum
18.01.2022
Beginn
18.01.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt
Extra dose administered Product administration error

Symptomtext

Medical Assistant administered entire multi-dose vial of covid-19 Pfizer vaccine into patient's right arm. Patient advised to monitor for signs and symptoms of anaphylaxis. Patient was given ER precautions. Patient denies any signs and symptoms at time of reporting.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Extra dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2043580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
HI
Alter
29,0
Geschlecht
F
Eingang
18.01.2022
Impfdatum
14.01.2022
Beginn
15.01.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
SYR / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Lymphadenopathy

Symptomtext

Swollen lymph nodes for a week.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Lymphadenopathy
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
None
Allergien
None
Vorherige Impfungen
-

VAERS 2043574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
34,0
Geschlecht
F
Eingang
18.01.2022
Impfdatum
14.01.2022
Beginn
15.01.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Eye swelling Swelling face Induration Swelling

Symptomtext

Swelling of facial hylauronic acid filler , and swelling of eyes.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Induration
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
None
Vorgeschichte
None
Andere Medikamente
Estrogen ring - generic version
Allergien
None
Vorherige Impfungen
-

VAERS 2038206

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj5683

gering
Staat
KS
Alter
46,0
Geschlecht
F
Eingang
16.01.2022
Impfdatum
13.01.2022
Beginn
15.01.2022
Tage bis Beginn
2,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Lymphadenopathy

Symptomtext

Left side supraclavicular lymphadenopathy.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Lymphadenopathy
Hospital-Tage
-
Labordaten
None
Aktuelle Erkrankungen
None
Vorgeschichte
No
Andere Medikamente
Yes-dietary supps such as vitamin D, biotin, calcium
Allergien
No
Vorherige Impfungen
-

VAERS 2035547

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
NH
Alter
72,0
Geschlecht
M
Eingang
14.01.2022
Impfdatum
14.01.2022
Beginn
14.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Feeling abnormal Unresponsive to stimuli

Symptomtext

Patient was in recovery area at the time, when his 15 min. was up to wait after his vaccination, when he was checked on, the patient was in a daze, not responding, but conscious. pt then became verbal/ lucid after approx. 1 minute afterwards, he was AAOX3. pt, denied any SOB, Chest pain, headache/dizziness/ N/V/D. pt lung clear to auscultation, pulse ox read O2 stat 99% on RA, Pulse 88, resp. 20. EMS was called while patient was being assessed, within 5 min. EMS arrived, care was then taken over by emergency services. pt was asked if he wanted to go to the hospital by EMS, pt. verbalized yes. patient was then transported out of the facility.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Feeling abnormal
Hospital-Tage
-
Labordaten
N/A at facility
Aktuelle Erkrankungen
A-Fib, COPD, Acid reflux
Vorgeschichte
A-FIB, COPD, Acid reflux current smoker, patient stated he smokes one pack of cigarettes a day
Andere Medikamente
unknown patient did not verbalize/ or share this information at this time
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2032604

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Fj5683

gering
Staat
IA
Alter
5,0
Geschlecht
M
Eingang
13.01.2022
Impfdatum
13.01.2022
Beginn
13.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered

Symptomtext

patient was intended to get the peds Pfizer does but inadvertently was given the Pfizer 12 year and up, no symptoms at this time

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
no allergies
Vorherige Impfungen
-

VAERS 2032593

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
IA
Alter
7,0
Geschlecht
M
Eingang
13.01.2022
Impfdatum
13.01.2022
Beginn
13.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / LL
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Incorrect dose administered

Symptomtext

Patient was intended to get age appropriate vaccine, patient was inadvertently given the Pfizer 12 and up, no symptoms at this time.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
Iron deficiency anemia
Andere Medikamente
Vitron C
Allergien
Bacitracin
Vorherige Impfungen
-

VAERS 2032320

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
TX
Alter
5,0
Geschlecht
F
Eingang
13.01.2022
Impfdatum
13.01.2022
Beginn
13.01.2022
Tage bis Beginn
0,0
Dosis
2
Route/Site
SYR / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Incorrect dose administered

Symptomtext

Patient was vaccinated with Pfizer .3

Weitere VAERSDATA-Felder
Praegender Schweregrund
Incorrect dose administered
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2028414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PA
Alter
44,0
Geschlecht
M
Eingang
12.01.2022
Impfdatum
10.01.2022
Beginn
10.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
No adverse event

Symptomtext

PATIENT WANTED TO GET THE MODERNA VACCINE BOOSTER BUT WAS GIVEN THE PFIZER COVID VACCINE BOOSTER. THE VACCINATOR ADMINISTERED THE PFIZER COVID VACCINE BOOSTER IN THE LEFT DELTOID WITH NO ISSUES. PT EXPRESSED DISMAY THAT HE GOT THE PFIZER BOOSTER ONCE HE WAS TOLD THAT HE GOT THE PFIZER BUT DID NOT HAVE ANY ADVERSE REACTIONS DURING HIS 15 MINUTE POST BOOSTER WAITING PERIOD.

Weitere VAERSDATA-Felder
Praegender Schweregrund
No adverse event
Hospital-Tage
-
Labordaten
NONE
Aktuelle Erkrankungen
none listed
Vorgeschichte
none listed
Andere Medikamente
not available
Allergien
none
Vorherige Impfungen
-

VAERS 2658697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
-
Alter
52,0
Geschlecht
F
Eingang
11.01.2022
Impfdatum
07.01.2022
Beginn
07.01.2022
Tage bis Beginn
0,0
Dosis
1
Route/Site
IM / RA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein
Conversion disorder Dyskinesia

Symptomtext

Narrative: functional neurological disorders (once called psychogenic) have been reported following COVID vaccination

Weitere VAERSDATA-Felder
Praegender Schweregrund
Conversion disorder
Hospital-Tage
-
Labordaten
Patient presents as a rapid response. There were some involuntary movements of her extremities, some bobbing back-and-forth. Patient reportedly on meds for seizure. She is neurovascularly intact in the ED. No seizure here in the ED. On chart review, from a note from neurology in 2019, assumed that patient's seizures were psychogenic nonepileptic seizures.
Aktuelle Erkrankungen
-
Vorgeschichte
-
Andere Medikamente
-
Allergien
-
Vorherige Impfungen
-

VAERS 2025105

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PR
Alter
12,0
Geschlecht
F
Eingang
11.01.2022
Impfdatum
08.01.2022
Beginn
08.01.2022
Tage bis Beginn
0,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Inappropriate schedule of product administration

Symptomtext

*ADMINISTRATION ERROR* 12 y/o female received her COVID-19 vaccine (Pfizer) booster on 1/8/2022. Her mother visited the vaccination center today, 1/11/2022, to notify that her daughter had received her vaccine before her recommended date, approximately 1 month before. Her second dose was administered on 9/2/2021 and based on most recent CDC guidelines, it is recommended that she wait 5 months before receiving her booster dose. In her case booster dose should have been administered no sooner than 2/2/2022. The event was notified and properly documented.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Inappropriate schedule of product administration
Hospital-Tage
-
Labordaten
N/A
Aktuelle Erkrankungen
N/A
Vorgeschichte
Sickle cell anemia
Andere Medikamente
N/A
Allergien
NKDA
Vorherige Impfungen
-

VAERS 2021335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
CA
Alter
14,0
Geschlecht
F
Eingang
10.01.2022
Impfdatum
09.01.2022
Beginn
10.01.2022
Tage bis Beginn
1,0
Dosis
3
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein
Hypoaesthesia oral Lip swelling

Symptomtext

Within 24 hours our daughter developed very swollen lips with a high degree of numbness

Weitere VAERSDATA-Felder
Praegender Schweregrund
Hypoaesthesia oral
Hospital-Tage
-
Labordaten
none
Aktuelle Erkrankungen
none
Vorgeschichte
none
Andere Medikamente
none
Allergien
none
Vorherige Impfungen
-

VAERS 2014310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge FJ5683

gering
Staat
PA
Alter
39,0
Geschlecht
F
Eingang
07.01.2022
Impfdatum
06.01.2022
Beginn
06.01.2022
Tage bis Beginn
0,0
Dosis
N/A
Route/Site
IM / LA
Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja
Interchange of vaccine products

Symptomtext

Vaccine Administration Error- Patient wanted a Moderna Booster (previously received Janssen as her primary series), however received a Pfizer Booster instead. Patient was understanding and did not seem to have any adverse effect.

Weitere VAERSDATA-Felder
Praegender Schweregrund
Interchange of vaccine products
Hospital-Tage
-
Labordaten
-
Aktuelle Erkrankungen
N/A
Vorgeschichte
N/A
Andere Medikamente
N/A
Allergien
N/A
Vorherige Impfungen
-