VAERS Reports GJ3275

VAERS 2728731

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ3275

kritisch

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 29.12.2023
Impfdatum: 07.12.2022
Beginn: 13.11.2023
Tage bis Beginn: 341,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Asthenia Blood culture Blood lactic acid normal COVID-19 Chest X-ray normal Pyrexia SARS-CoV-2 test positive Sepsis White blood cell count normal

Symptomtext

Patient is a 83 y.o. male patient of MD with history of Melanoma, hyperthyroidism, C.Diff, HTN, IBS, WPW, LBBB, Prostate CA s/p RT, radiation proctitis presented to Medical Center with fever and weakness . Acute hypoxemic resp failure - resolved COVID-19 Date of onset of symptoms: ~11/12 Symptoms present on admission: fever; weakness Date of covid positive test: 11/13 Vaccination status: vaccinated ICXR unremarkable on admission Oxygen requirements on admission: 3L Current oxygen requirements: 3L Medical therapy: Steroids and Remdesivir Consultants following: none Anticipated special isolation end date: tentatively 11/21 11/16: Patient currently on room air. Started Remdesvir 11/14, currently on day 3 of 4 but requesting discharge at this time stating his symptoms have resolved and breathing is back to baseline. Patient informed if discharged he would miss final dose to which he stated he understood and would like to go home. Patient to follow up with PCP upon hospital discharge. Will discharge on Decadron for a total of 10 days. Sepsis POA with fever and resp failure Likely viral due to COVID WBC and lactate wnl Hemodynamically stable CXR unremarkable BCx ordered Holding off ABx for now HTN Cont home Norvasc, Cozaar, BB with holding parameters Chronic proctitis Currently stable Cont home Canasa

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2726893

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 22.12.2023
Impfdatum: 31.10.2022
Beginn: 18.09.2023
Tage bis Beginn: 322,0
Dosis: 1
Route/Site: - / -

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

Acute kidney injury Acute respiratory distress syndrome Acute respiratory failure Asthenia Atrial fibrillation COVID-19 pneumonia Chest discomfort Dyspnoea Echocardiogram normal Ejection fraction normal General physical condition abnormal Hypoxia Myocardial ischaemia Pyrexia Troponin increased

Symptomtext

Patient is a 65 y.o. male presenting from home with c/o 65 y.o. male who presents with a chief complaint of SOB. Patient is a 65-year-old male who presents with daughter for evaluation of fever, generalized weakness, shortness of breath. Per daughter, patient had just arrived after a week long cruise. Daughter states she picked him up from the airport and noticed that he appeared ill. She states she drove patient directly to the hospital. Patient reports shortness of breath, generalized weakness, with some mild chest discomfort. Daughter states patient not normally on home O2. Patient hypoxic on room air and required and received my immediate medical attention. Hospital course as below. Original plan was discharged to LTAC but oxygen requirements improved and patient was able to be discharged home with home health care services 1. COVID pneumonia, ARDS: -+9/18 -Unclear symptom onset, isolation completed -Pulmonology following -Infectious disease saw pt -Decadron 10 day course completed 9/28 -Remdesivir completed 9/28 -DVT prophylaxis with lovenox -completed 10 day course of zosyn for possible bacterial coverage -pulm rehab at discharge: will be arranged by Dr. 2. Acute hypoxic respiratory failure: -Secondary to above -Pulmonology following -home O2 concentrator arranged with SW 3. AKI: resolved -Nephrology consulted -monitor labs -Received fluids -hold nephrotoxic agents -EP recommended stopping Tikosyn, cardio re-consulted once AKI resolved and decided not to restart tikosyn and re-eval with EP outpatient 4. Elevated troponin -Cardiology consulted, likely type II/demand ischemia in the setting of acute illness -Plans for stress test outpatient when patient recovered -9/19 echo EF 60% 5. A-fib: -Cardiology consulted -See recommendation above in regards to Tikosyn 6. CLL, immunocompromise: -Follows with oncology -Oncology consulted, advised holding home oral chemo at this time until acute issues resolve 7. Other chronic medical conditions: Chronic pain, anxiety, arthritis, hypertension, peripheral neuropathy, OSA unable to tolerate CPAP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 29,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2726716

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: AZ
Alter: 82,0
Geschlecht: M
Eingang: 21.12.2023
Impfdatum: 13.10.2022
Beginn: 23.02.2023
Tage bis Beginn: 133,0
Dosis: 1
Route/Site: IM / LA

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

Abdominal tenderness Acute respiratory failure Blood lactic acid increased Blood loss anaemia COVID-19 Chills Computerised tomogram abdomen abnormal Cough Dyspnoea Faeces discoloured Haematochezia Haematuria Haemorrhagic disorder Headache Ileus Lower gastrointestinal haemorrhage Pneumonia Pyrexia

Symptomtext

Reported Symptoms: 10011232:COUGHING; 10016558:FEVER; 10019211:HEADACHE; 10043088:TACHYPNEA; Narrative: ASSESSMENT & PLAN: 82 y/o Male with Hx of Colon CA s/p partial colectomy, ileostomy, DVT/PE on anticoagulation who presents with dark and bloody stool x 3 days here for suspected GI bleed ACUTE: #GI bleed (suspect lower) #Acute blood loss anemia 2/2 above #COVID-19 positive, chronic - precautions cleared by ID #acute on chronic hypoxic respiratory failure #iatrogenic bleeding disorder 2/2 AC for chronic PE/DVT #Type II DM on insulin # hematuri Other Relevant HX: Patient is an 82 yo who presents to the ED FEB 23,2023@ 02:19:37 Subjective/Chief Complaint: Pt to ED with c/o onset fever, chills, cough, headache, and SOB ~ 2 hours ago. States just got back from traveling yesterday. ED Physician: diabetic, travelling, hypoxic now, covid +, PNA, UTI, mild ileus on CT Abd. Tachy, 2 l of fluid, Rocephin, lactic acid elevated. MRSA positive. Colon CA with colostomy mild abd tenderness. Other:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2721042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: MN
Alter: 48,0
Geschlecht: F
Eingang: 05.12.2023
Impfdatum: 12.12.2022
Beginn: 01.11.2023
Tage bis Beginn: 324,0
Dosis: 4
Route/Site: IM / RA

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

Acute respiratory failure COVID-19 COVID-19 pneumonia Chemotherapy Dyspnoea Fatigue Headache Plasma cell myeloma Pyrexia SARS-CoV-2 test positive Septic shock

Symptomtext

The patient was seen in the ED on 11/1/23 with shortness of breath, fatigue, headache, and fever that began earlier that evening. Additionally, she was recently diagnosed with multiple myeloma and was started on her first dose of chemotherapy 24 hours prior. A COVID-19 Rapid PCR test was done int he ED which resulted positive. Ultimately, she was admitted 11/1/23 - 11/6/23. Discharge diagnoses included septic shock and acute hypoxemic respiratory failure secondary to COVID-19 pneumonia, among other diagnoses. She required supplemental oxygen via nasal cannula but was weaned off several days prior to discharge. Of note, the patient has received the Pfizer monovalent COVID vaccine (given 4/10/21; 5/1/21; 3/3/22) and the Pfizer Bivalent COVID vaccine (given 12/12/22).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2574664

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

kritisch

Staat: IL
Alter: 67,0
Geschlecht: M
Eingang: 29.10.2023
Impfdatum: 25.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Aphasia Blood test Cerebrovascular accident Computerised tomogram Dysphagia Economic problem Laboratory test Loss of personal independence in daily activities Magnetic resonance imaging Musculoskeletal disorder Haemorrhagic stroke Paralysis Speech disorder Wrong product administered

Symptomtext

I received the Pfizer Covid 19 Booster on 10-25-2022. 4 hours later, I lost the use of my left leg. I was promptly taken to the hospital ER. Shortly later I lost the use of my left arm, speech and swallowing. I was in the hospital for 22 days. I received PT, OT and speech thereapy while there. I was discharged and have continued 2 times a week theraphy at Outpatient facility. At the time of the stroke, I was gainfully employed as a property insurance adjuster. I maintained my house inside and outside for all upkeep and maintence. I now have to hire some one to do it. I was very active with my grandchildren, sportsman-fishing, helping friends build and remodel homes. I have had to make several withdraws from the retirement in order to pay medical bills, household expenses and purchase medical equipment for my home so that I am safe. My left arm and leg will not allow me to proceed with my previous lifestyle.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 22,0
Labordaten: CT's, MRI's, laboratory testing, blood testing, Began 10-25-2022 and continuing
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Omeprazole, Lisinpril, Eliquis
Allergien: None
Vorherige Impfungen: -

VAERS 2660038

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: MN
Alter: 76,0
Geschlecht: M
Eingang: 24.07.2023
Impfdatum: 24.10.2022
Beginn: 14.05.2023
Tage bis Beginn: 202,0
Dosis: N/A
Route/Site: IM / LA

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

Asthenia COVID-19 Cerebrovascular accident Cough Dyspnoea Palpitations SARS-CoV-2 test positive Symptom recurrence

Symptomtext

The patient has a history of chronic atrial fibrillation and COPD. Notably, he was recently hospitalized 4/22/23 - 5/3/23 for recurrent right MCA CVA. On 5/14 the patient presented to the ED due to increased weakness, shortness of breath, and palpitations. A COVID PCR test performed in the ED resulted positive. Ultimately, he was admitted 5/14/23 - 5/16/23 for cough and generalized weakness likely secondary to COVID-19 infection, among other discharge diagnoses. Of note, the patient remained on room air throughout his admission. He has received the primary COVID vaccine series and three boosters.

Weitere VAERSDATA-Felder

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

VAERS 2654287

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: -
Alter: 82,0
Geschlecht: M
Eingang: 10.07.2023
Impfdatum: 09.11.2022
Beginn: 07.02.2023
Tage bis Beginn: 90,0
Dosis: 4
Route/Site: IM / RA

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

Acute respiratory failure Respiratory failure Symptom recurrence

Symptomtext

ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPERCAPNIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 2/1/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2637045

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

kritisch

Staat: MO
Alter: 58,0
Geschlecht: M
Eingang: 26.05.2023
Impfdatum: 17.12.2022
Beginn: 15.04.2023
Tage bis Beginn: 119,0
Dosis: 3
Route/Site: - / -

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

Sudden cardiac death

Symptomtext

Died Suddenly Cardiac Event

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Praegender Schweregrund: Sudden cardiac death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Felt unwell and ?not right? after second Covid shot prior to the booster shot

VAERS 2634863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: TN
Alter: 54,0
Geschlecht: M
Eingang: 22.05.2023
Impfdatum: 02.11.2022
Beginn: 01.03.2023
Tage bis Beginn: 119,0
Dosis: 5
Route/Site: IM / RA

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

Atelectasis Bronchial secretion retention Bronchoscopy Chest X-ray abnormal Death Hypotension Mechanical ventilation Oxygen saturation decreased Pulse absent Sepsis Tracheostomy

Symptomtext

The patient initially weaned off the ventilator but then developed an episode of sepsis and never was able to tolerate significant weaning subsequently. He had an event desaturation on trach collar on 05/17. Chest x-ray showed mucus plugging left lung. Despite aggressive percussive therapy, he left lung remained atelectatic. Bronchoscopy was performed the morning of 5/18. The mucus plug was removed and he had temporary improvement in his oxygenation. However he became profoundly hypotensive requiring pressor therapy. Multiple attempts were made to obtain labs without success. Broad-spectrum antibiotics were initiated. Discussions were held with his parents and siblings. They understood his severity of illness and elected to change his code status to DNR/active. He he became pulseless despite maximal ventilator support and pressor therapy and expired with family present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Quadriplegia at C5-C6 level due to MVA in 1995 Hypertension Hyperlipidemia OSA on home CPAP Neurogenic bladder Morbid obesity Sacral decubitus ulcer Sinus node dysfunction status post permanent pacer placement Baclofen pump for spasticity Hypothyroidism
Andere Medikamente: -
Allergien: Adhesive
Vorherige Impfungen: -

VAERS 2634472

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

kritisch

Staat: NY
Alter: 80,0
Geschlecht: M
Eingang: 20.05.2023
Impfdatum: 22.01.2021
Beginn: -
Tage bis Beginn: -
Dosis: 6
Route/Site: OT / -

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

Ascites Biopsy bone Cardiac arrest Condition aggravated Haemoglobin Hepatic necrosis Myelodysplastic syndrome Pleural effusion Pneumonia

Symptomtext

pleural effusion; peritoneal effusion/Patient has minimal fluid in the lung area. Patient got an abdominal peritoneal fluid.; preleukemia/ Each of the biopsy show know cancer. The abnormal T cell are inhibiting the production of red blood cell/ anemic; pneumonia/Patient had 3 chest cap; cardiac arrest; Patient got some necrosis showing in his liver; had a ripple effect after his first Moderna vaccine; This spontaneous case was reported by a patient family member or friend and describes the occurrence of MYELODYSPLASTIC SYNDROME (preleukemia/ Each of the biopsy show know cancer. The abnormal T cell are inhibiting the production of red blood cell/ anemic), PNEUMONIA (pneumonia/Patient had 3 chest cap), CARDIAC ARREST (cardiac arrest), PLEURAL EFFUSION (pleural effusion), ASCITES (peritoneal effusion/Patient has minimal fluid in the lung area. Patient got an abdominal peritoneal fluid.) and HEPATIC NECROSIS (Patient got some necrosis showing in his liver) in an 80-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 013L2BA, 016M20A, 939904 and 855822A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for an unknown indication. Patient had no allergies. Patient did have medical history before receiving the vaccine. Concurrent medical conditions included Social alcohol drinker. On 22-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 19-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 22-Oct-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 22-Aug-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 04-Nov-2022, the patient received fifth dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On 08-May-2023, received sixth dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced MYELODYSPLASTIC SYNDROME (preleukemia/ Each of the biopsy show know cancer. The abnormal T cell are inhibiting the production of red blood cell/ anemic) (seriousness criteria hospitalization, medically significant and life threatening), PNEUMONIA (pneumonia/Patient had 3 chest cap) (seriousness criteria hospitalization, medically significant and life threatening), CARDIAC ARREST (cardiac arrest) (seriousness criteria hospitalization, medically significant and life threatening), PLEURAL EFFUSION (pleural effusion) (seriousness criteria hospitalization and life threatening), ASCITES (peritoneal effusion/Patient has minimal fluid in the lung area. Patient got an abdominal peritoneal fluid.) (seriousness criteria hospitalization, medically significant and life threatening), HEPATIC NECROSIS (Patient got some necrosis showing in his liver) (seriousness criterion medically significant) and CONDITION AGGRAVATED (had a ripple effect after his first Moderna vaccine). The patient was hospitalized for 10 days due to CARDIAC ARREST. The patient was treated with CICLOSPORIN (CYCLOSPORINE) at an unspecified dose and frequency; DARBEPOETIN ALFA (ARANESP) at a dose of for 3 months and METHOTREXATE at a dose of for 3 months. At the time of the report, MYELODYSPLASTIC SYNDROME (preleukemia/ Each of the biopsy show know cancer. The abnormal T cell are inhibiting the production of red blood cell/ anemic), PNEUMONIA (pneumonia/Patient had 3 chest cap), CARDIAC ARREST (cardiac arrest), PLEURAL EFFUSION (pleural effusion), HEPATIC NECROSIS (Patient got some necrosis showing in his liver) and CONDITION AGGRAVATED (had a ripple effect after his first Moderna vaccine) outcome was unknown and ASCITES (peritoneal effusion/Patient has minimal fluid in the lung area. Patient got an abdominal peritoneal fluid.) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 11-May-2023, Haemoglobin: hemoglobin last Thursday was 6.8.. On an unknown date, Biopsy bone: Had 4 bone biopsies. Each of the biopsy showed non cancerous T cell, that are inhibiting the production of red blood cell.. No concomitant medications were reported. It was reported that the patient has not had any problem before the vaccine. He was extremely anemic when he went for his routine physical exam. They found non-cancerous T cell in this bone marrow. He went to the emergency room and his heart stoped. He had a cardiac arrest. He spent 10 days in ICU. He had a variety of issues in March 2022. This started 6 months ago, he was dealing with lung and liver process. He was stable cardiac and pulmonary wise. His anemia persisted. They try 4 other drugs. In the last year he had 70 transfusions. All this started after the 1st dose of the Moderna vaccine. While patient was in ICU for the pneumonia, he develops a pleural effusion. Patient's brother believes this could be the residual of the pneumonia. Every two-week patient had his abdomen tap. About 3 to 5 liter of fluids was removed from his abdomen. Last week it was 5 liters. Patient continued to accumulate fluid. His abdominal tap had been going on for months. Before they did not know where the fluid was coming from. Now, they were saying from his liver. Patient heart and lung were fine but still had the abnormal T cell. Company comment: This is a Spontaneous case reported by a consumer, concerning an 80-year-old male patient, with no relevant medical history, who experienced the unexpected and serious (due to life-threatening, hospitalization and medically significant) events of Myelodysplastic syndrome, Pneumonia, Cardiac arrest and Ascites, the unexpected and serious (due to hospitalization and medically significant) event of Pleural effusion, and the unexpected and serious (due to medically significant) AESI of Hepatic necrosis, which occurred on an unknown date after the first dose of mRNA-1273 vaccine. Second, third and fourth doses against COVID-19 were administered with mRNA-1273, and fifth and sixth with Pfizer vaccine, which remains as a co-suspect product. As reported, patient was extremely anemic when he went for his routine physical exam. Non-cancerous T cells were found in his bone marrow. He was diagnosed with preleukemia and was prescribed cyclosporine. He got pneumonia and went to the emergency room where his heart stopped. He spent 10 days in intensive care unit, where he developed pleural and peritoneal effusion. His liver had necrosis. Since then, 3 to 5 liters of fluid are removed from patient?s abdomen. Last hemoglobin was 6.8. In the last year patient had 70 transfusions. He had 4 bone biopsies. Each of the biopsies showed no cancer. The abnormal T cells are inhibiting the production of red blood cell. Patient was prescribed Cyclosporine, Darbepoetin alfa and Methotrexate. At the time of the report, Myelodysplastic syndrome, Pneumonia, Cardiac arrest, Pleural effusion, Hepatic necrosis and Condition aggravated outcome was unknown, and Ascites had not resolved. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This is a Spontaneous case reported by a consumer, concerning an 80-year-old male patient, with no relevant medical history, who experienced the unexpected and serious (due to life-threatening, hospitalization and medically significant) events of Myelodysplastic syndrome, Pneumonia, Cardiac arrest and Ascites, the unexpected and serious (due to hospitalization and medically significant) event of Pleural effusion, and the unexpected and serious (due to medically significant) AESI of Hepatic necrosis, which occurred on an unknown date after the first dose of mRNA-1273 vaccine. Second, third and fourth doses against COVID-19 were administered with mRNA-1273, and fifth and sixth with Pfizer vaccine, which remains as a co-suspect product. As reported, patient was extremely anemic when he went for his routine physical exam. Non-cancerous T cells were found in his bone marrow. He was diagnosed with preleukemia and was prescribed cyclosporine. He got pneumonia and went to the emergency room where his heart stopped. He spent 10 days in intensive care unit, where he developed pleural and peritoneal effusion. His liver had necrosis. Since then, 3 to 5 liters of fluid are removed from patient?s abdomen. Last hemoglobin was 6.8. In the last year patient had 70 transfusions. He had 4 bone biopsies. Each of the biopsies showed no cancer. The abnormal T cells are inhibiting the production of red blood cell. Patient was prescribed Cyclosporine, Darbepoetin alfa and Methotrexate. At the time of the report, Myelodysplastic syndrome, Pneumonia, Cardiac arrest, Pleural effusion, Hepatic necrosis and Condition aggravated outcome was unknown, and Ascites had not resolved. The benefit-risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: Test Name: 4 bone biopsies; Result Unstructured Data: Had 4 bone biopsies. Each of the biopsy showed non cancerous T cell, that are inhibiting the production of red blood cell.; Test Date: 20230511; Test Name: hemoglobin; Result Unstructured Data: hemoglobin last Thursday was 6.8.
Aktuelle Erkrankungen: Social alcohol drinker
Vorgeschichte: Comments: Patient had no allergies. Patient did have medical history before receiving the vaccine.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2614112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: MN
Alter: 72,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 21.10.2022
Beginn: 08.03.2023
Tage bis Beginn: 138,0
Dosis: 5
Route/Site: IM / LA

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

Arterial occlusive disease Arteriogram coronary abnormal Asthenia Chest X-ray abnormal Chest pain Computerised tomogram thorax abnormal Condition aggravated Coronary angioplasty Coronary arterial stent insertion Cough Diabetic ketoacidosis Electrocardiogram abnormal Fatigue Influenza virus test negative Laboratory test normal Malaise Myocardial infarction Pericardial effusion

Symptomtext

I woke up with a fever, a bad cough, and chest pain. I thought I was just sick. I kind of hoped it would just get better. The symptoms continued; the chest pain diminished, but the coughing and fever continued for the next three days. I went to urgent care on 3/11/2023. I underwent tests for COVID-19, streptococcus, pneumonia, and the flu. I underwent a chest X-ray. I was diagnosed with an upper respiratory infection after I tested negative on all of those. I was prescribed an antibiotic whose name I don't remember. The symptoms did not improve. On 3/15/2023, I called the nurse line and told them that my symptoms hadn't improved, and I was instructed to go to the ER. At the ER, I was tested for COVID-19 and various other illnesses, and the results were all negative. I underwent a chest CT scan, which showed fluid around my heart and lungs. The ER doctor told me that this was concerning and that I should see with my PCP soon. On 3/17/2023, I saw my PCP, who did an EKG that showed I was having a heart attack. She called an ambulance, and I was sent to the ER. At the ER, an angiogram was done, which showed that I had a main artery that was 100% blocked. Two stents were put into the artery, and a balloon was also placed somewhere. I was admitted to the hospital and stayed two days. On 4/3/2023 and 4/4/2023, I was in the hospital again, this time for diabetic ketoacidosis. I am currently on insulin, and I was given IV fluids to treat the ketoacidosis. At the time of this writing, I am still weak and tired. I am now going cardiac rehab twice a week; I will be doing this for 18 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 4,0
Labordaten: 11MAR2023 - COVID-19, Streptococcus, Pneumonia, Flu Tests - All Negative Results; 11MAR2023 - Chest X-Ray - Upper Respiratory Infection Diagnosed; 15MAR2023 - COVID-19, Streptococcus, Pneumonia, Flu Tests - All Negative Results; 15MAR2023 - Chest CT Scan - Fluid Around Heart and in Lungs Detected; 17MAR2023 - EKG - Heart Attack Detected; 17MAR2023 - Angiogram - 100% Blockage of Main Artery Detected
Aktuelle Erkrankungen: None
Vorgeschichte: Chronic Fatigue Syndrome; Gastroesophageal Reflux Disease; Sleep Apnea; Chronic Kidney Disease; Diabetes, Type II; Gout; Ataxia; History of Heart Attack (Two Stents Placed); Diabetic Ketoacidosis; Hypertrophic Cardiomyopathy; Pericarditis
Andere Medikamente: Allopurinol; Baclofen; Calcium with Vitamin D; Cephalexin; Chlorthalidone; Vitamin B12; Duloxetine; Glipizide; Melatonin; Mirtazapine; Omeprazole; Trulicity; Valsartan
Allergien: Sulfa Drugs; Influenza Vaccine; Trazodone; Colcrys; Fludrocortisone; Midodrine; Lisinopril; Metformin; Atorvastatin; Doxycycline
Vorherige Impfungen: -

VAERS 2613388

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: DE
Alter: 59,0
Geschlecht: F
Eingang: 11.04.2023
Impfdatum: 10.10.2022
Beginn: 06.04.2023
Tage bis Beginn: 178,0
Dosis: 5
Route/Site: IM / AR

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

Acute myocardial infarction Arrhythmia Blood test abnormal Dizziness Echocardiogram Electrocardiogram Heart rate increased Myocardial necrosis marker increased Visual impairment

Symptomtext

On 04/06/2023, I had exercised for an hour and was about to go shopping. I was in a store, and I suddenly felt like I was going to black out. Everything went black before my eyes briefly. I went to my car until I felt ok to drive home. On my way home, I could tell my heart was out of rhythm. When I got home, my pulse was at 185. I tried some maneuvers that I've been taught to get my pulse down myself. When that was unsuccessful, I called an ambulance. I was transported to a local hospital. From there, I was in the emergency room for a long time. They decided on my blood work, to admit me. My cardiac enzymes were rising, so they admitted me on an observational basis. I was discharged the next day and saw my cardiologist who said that I had a type 2 myocardial infarction based on the elevated heart rate. He did some medication changes, and I will follow up with him to discuss further options.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: 1,0
Labordaten: 06APR2023 Blood work, elevated Cardiac Enzymes; Multiple EKG results unknown; 07APR2023 Blood work, elevated Cardiac Enzymes; Echocardiogram results unknown
Aktuelle Erkrankungen: None
Vorgeschichte: Supraventricular Tachycardia
Andere Medikamente: Metoprolol tartrate
Allergien: Metal
Vorherige Impfungen: -

VAERS 2609078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: WI
Alter: 77,0
Geschlecht: F
Eingang: 04.04.2023
Impfdatum: 17.11.2022
Beginn: 04.02.2023
Tage bis Beginn: 79,0
Dosis: 3
Route/Site: UN / UN

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

Acute respiratory failure Asthma Breath sounds abnormal COVID-19 Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Dyspnoea Hypoxia Lung opacity SARS-CoV-2 test positive Wheezing

Symptomtext

Late in the evening on 2/4/2023, patient presented to the emergency department via ambulance from the nursing home for evaluation of shortness of breath, hypoxia with oxygen saturations in the high 60s at the nursing home, and a positive COVID-19 test at the nursing home. In the emergency department on 2/5/2023 just after midnight, patient was given a COVID-19 NAA test which resulted positive; Her chest x-ray showed minimal bibasilar opacities consistent with COVID-19 infection; She had dyspnea with audible wheezing and coarse breath sounds. Patient was treated with supplemental oxygen, DuoNeb nebulizer, and steroids. She was diagnosed with acute respiratory failure with hypoxemia, COVID-19 virus infection, and COPD/asthma exacerbation. Patient was admitted to the hospital for further evaluation and treatment. Submitter does not have access to further medical information on this case including discharge date. If more information is needed, please contact the admitting hospital:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: 2/5/2023 - positive COVID-19 NAA test; Chest x-ray showed minimal bibasilar opacities consistent with COVID-19 infection.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: COPD with asthma, chronic kidney disease stage IV, hypertension, hyperlipidemia, dementia, expressive aphasia, depression, anxiety, acid reflux.
Andere Medikamente: Unknown
Allergien: Patient has allergies to gluten, penicillin, and tolmetin.
Vorherige Impfungen: -

VAERS 2607524

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: IL
Alter: 85,0
Geschlecht: M
Eingang: 31.03.2023
Impfdatum: 26.10.2022
Beginn: 01.03.2023
Tage bis Beginn: 126,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Death

Symptomtext

Died of complications to COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: Medical Examiner report
Aktuelle Erkrankungen: Complications of prostate cancer; OSC: COVID-19; CHF; CAD; DM2; CKD stage 3; PVD; HTN; HLD; obesity
Vorgeschichte: Complications of prostate cancer; OSC: COVID-19; CHF; CAD; DM2; CKD stage 3; PVD; HTN; HLD; obesity
Andere Medikamente: Unknown by recorder
Allergien: Unknown by recorder
Vorherige Impfungen: -

VAERS 2604966

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: WI
Alter: 75,0
Geschlecht: F
Eingang: 28.03.2023
Impfdatum: 03.11.2022
Beginn: 17.01.2023
Tage bis Beginn: 75,0
Dosis: 4
Route/Site: UN / UN

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

Acute respiratory failure Acute right ventricular failure Atrial enlargement COVID-19 Cardiac arrest Central venous catheterisation Chronic right ventricular failure Computerised tomogram head normal Death Endotracheal intubation Hypotension Intensive care Lung disorder Pulmonary oedema Pulseless electrical activity Respiratory failure Resuscitation Right-to-left cardiac shunt

Symptomtext

1/17/2023: Became unresponsive after walking back from an echochardiogram appointment. Received CPR and transported to the ED. ACLS was continued for 10 minutes approximately before ROSC, 3 doses of epinephrine were given. She was intubated and central line placed. Had another cardiac arrest for around 4 minutes despite multiple pressors started when patient was getting hypotensive. Arrives to ICU on NE and epinephrine , diffuse B lines in all lung zones. IVC plethoric Family reported DNR/DNI status, changed to comfort measures. Patient expired on 1/18/2023. HOSPITAL PROBLEM LIST: 1. Resuscitated cardiac arrest 2. PEA cardiac arrest 3. Acute on chronic hypoxemic respiratory failure 4. Diffuse pulmonary edema on lung ultrasound 5. Acute on chronic RV failure 6. Severe biatrial enlargement 7. Right to left cardiac shunt 8. Pulmonary artery hypertension group 1&3 9. COPD-moderate 10. Tobacco use history 11. DM 12. Dementia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 1,0
Labordaten: 1/17/2023: CT head without acute intracranial abnormality. 1/18/2023: Covid-19 detected per NAA
Aktuelle Erkrankungen: unknown
Vorgeschichte: PMH of chronic hypoxemic respiratory failure on 6 lts O2 via NC, COPD and pulmonary HTN
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2577360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: MN
Alter: 76,0
Geschlecht: F
Eingang: 07.02.2023
Impfdatum: 25.10.2022
Beginn: 02.12.2022
Tage bis Beginn: 38,0
Dosis: 5
Route/Site: IM / RA

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

Acute respiratory failure Asthenia Bronchitis COVID-19 Chronic obstructive pulmonary disease Cough Dyspnoea Malaise SARS-CoV-2 test positive

Symptomtext

Patient seen in the ED on 12/2/22 for weakness. Patient has been feeling ill for the past several days, and on 11/28/22 tested positive for COVID. She does wear 2L home oxygen. She has been getting progressively weaker, and reports cough and shortness of breath. COVID PCR test done in the ED also resulted positive. Ultimately she was admitted 12/2/22 - 12/7/22 for COVID-19 infection, acute bronchitis, acute on chronic respiratory failure, and COPD.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2577319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: MI
Alter: 78,0
Geschlecht: M
Eingang: 07.02.2023
Impfdatum: 03.01.2023
Beginn: 23.01.2023
Tage bis Beginn: 20,0
Dosis: 5
Route/Site: - / -

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

COVID-19 Cerebral haemorrhage Fall

Symptomtext

Hospital Principal Problem (Discharge Diagnoses): 1. Intraparenchymal hemorrhage of brain 2. COVID-19 infection 3. Neuropathy bilateral lower extremirties 4. Hypertrophic cardiomyopathy 5. HTN 6. Hypertrophic cardiomyopathy 7. Fall 8. Permanent atrial fibrillation 9. Hyperlipidemia 10.Type 2 diabetes mellitus 11.BPH 12.Overweight

Weitere VAERSDATA-Felder

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

VAERS 2576459

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: VA
Alter: 67,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 03.11.2022
Beginn: 21.12.2022
Tage bis Beginn: 48,0
Dosis: 5
Route/Site: SYR / LA

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

Angina pectoris Anticoagulant therapy Catheterisation cardiac Chest discomfort Coronary artery dissection Echocardiogram Electrocardiogram Myocardial infarction Myocardial necrosis marker Pain in extremity Pain in jaw

Symptomtext

I had jaw pain, chest pressure, and left arm pain one evening. I had been heart pain as well so I called 911 and was taken to the hospital. There, I was put under several exams including cardiac enzyme testing, EKG, echocardiogram, and heart catheterization and was informed I suffered from spontaneous coronary heart dissection, or a heart attack. I spent two nights in coronary care unit. I was given heparin and aspirin as well as PLAVIX. I was prescribed CRESTOR during discharge until my follow-up appointment with my cardiologist. Currently, I'm doing better until my next appointment for better accuracy of diagnosis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 2,0
Labordaten: Cardiac Enzymes, EKG, and Echocardiogram: 21Dec2022. Heart Catheterization: 22Dec2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: BONIVA; multivitamin; vitamin B12; magnesium; RELAFEN
Allergien: Sulfa drugs; bee stings
Vorherige Impfungen: -

VAERS 2572156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 31.01.2023
Impfdatum: 14.11.2022
Beginn: 30.12.2022
Tage bis Beginn: 46,0
Dosis: 1
Route/Site: - / -

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

Acute respiratory failure Blood bicarbonate increased Blood pH normal COVID-19 Chest X-ray abnormal Chills Constipation Decreased appetite Dyspnoea Lung disorder Malaise PCO2 increased Respiratory failure SARS-CoV-2 test positive Sepsis

Symptomtext

Patient is a 76 y.o. male patient of MD with history of hypothyroidism, CAD, HLD, HTN, asthma, chronic cough, and former tobacco use. Presents with SOB, chills, decreased appetite. Acute hypercapnic/hypoxic respiratory failure HHF on admission VBG w/ pH 7.36, pCO2 62.2, HCO3 34.9 CXR: left sided airspace disease, prominence of hilar region Respiratory status worse1/3-1/6 Now improving, weaned to NC on 1/11 Scheduled/PRN nebs, Pred taper On NC, autopap at night DC w oxygen, home O2 eval ordered for 1/13 Needs OP pulm f/u and PFT Patient qualifies for home O2 Covid-19 Virus Infection Sx onset 12/27/22, positive 12/29/22 Out of isolation on 1/7/23 Was symptomatic w respiratory failure Treated w remdesivir and steroids Hypothyroidism Continue home Synthroid 88mcg HTN Holding metoprolol, hyzaar in setting of sepsis Home meds: metoprolol 25mg at bedtime, hyzaar Gradually reintroduce meds as able/needed Monitor BP CAD HLD Daily ASA, Rosuvastatin Asthma No formal PFT Consider PFT outpatient GERD Endorses use of Nexium at home Protonix daily Constipation Last bowel movement on 01/12/23 Increase bowel regimen

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 14,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2565651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge gj3275

kritisch

Staat: TN
Alter: 77,0
Geschlecht: F
Eingang: 23.01.2023
Impfdatum: 06.12.2022
Beginn: 22.01.2023
Tage bis Beginn: 47,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Death Vaccine breakthrough infection

Symptomtext

COVID-related death, breakthrough case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: non-small cell cancer of lung, intractable N/V, pneumonia
Vorgeschichte: COPD, asthma, HTN
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2564158

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

kritisch

Staat: CA
Alter: -
Geschlecht: M
Eingang: 20.01.2023
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

Cerebrovascular accident Interchange of vaccine products Investigation Suspected COVID-19

Symptomtext

three shots from Moderna and 4th booster was Pfizer; stroke; had whole bunch of long Covid issues come back; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 52-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), as dose 4 (booster), single (Lot number: GJ3275) for covid-19 immunisation. The patient's relevant medical history included: "long covid " (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Moderna (Dose 1, single), for COVID-19 Immunization; Moderna (Dose 2, single), for COVID-19 Immunization; Moderna (Dose 3, single), for COVID-19 Immunization; Flu shot, for immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown", described as "three shots from Moderna and 4th booster was Pfizer"; CEREBROVASCULAR ACCIDENT (medically significant), 21 days after the suspect product(s) administration, outcome "unknown", described as "stroke"; SUSPECTED COVID-19 (non-serious), outcome "unknown", described as "had whole bunch of long Covid issues come back". The events "stroke" and "had whole bunch of long covid issues come back" required emergency room visit. The patient underwent the following laboratory tests and procedures: stomach test: Unknown results. Clinical course: 21 days after the patient had the Pfizer Booster, the 4th booster, the patient had the stroke. A day after he had the vaccine he was in the emergency room, and had whole bunch of long Covid issues come back immediately when he had the Pfizer vaccine. The patient never had the Pfizer product before Moderna was only fine the booster he had. They all last to week emergency room said the patient must have the adverse reaction to vaccine and it stop after that and eventually the Pfizer anticipated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: Test Name: stomach test; Result Unstructured Data: Test Result:Unknown results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Long COVID-19
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2511688

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 19.01.2023
Impfdatum: -
Beginn: 29.10.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: SYR / UN

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

Death Eye movement disorder Loss of consciousness Respiratory arrest Syncope Respiration abnormal Resuscitation

Symptomtext

stopped breathing; out walking, collapsed; eyes rolled back; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). Other Case identifier(s): 2022SA509379. A 67-year-old female patient (not pregnant) received BNT162b2 (BNT162B2 NOS), as dose number unknown, single (Batch/Lot number: unknown) at the age of 67 years for covid-19 immunisation; influenza vaccine inact split 4v (FLUZONE HIGH DOSE QUADRIVALENT), as dose number unknown, single (Batch/Lot number: unknown) for immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: EYE MOVEMENT DISORDER (death) with onset 29Oct2022, outcome "fatal", described as "eyes rolled back"; LOSS OF CONSCIOUSNESS (death, medically significant) with onset 29Oct2022, outcome "fatal", described as "out walking, collapsed"; RESPIRATORY ARREST (death, medically significant) with onset 29Oct2022, outcome "fatal", described as "stopped breathing". The patient date of death was 29Oct2022. Reported cause of death: "stopped breathing", "eyes rolled back", "out walking, collapsed". It was not reported if an autopsy was performed. Clinical course: On an unknown date, the patient received a dose of suspect influenza quadrivial A-B high dose HV vaccine and Pfizer biontech Covid-19 vaccine via unknown route in unknown administration site of Prophylactic vaccination. On 29Oct2022 the patient who went out walking, collapsed (loss of consciousness), eye roiled back (eye movement disorder) and stopped breathing (respiratory arrest) (unknown latency) following the administration of Pfizer biontech covid-19 vaccine. Final diagnosis was (fatal) stopped breathing. It was not reported the patient received a corrective treatment for the events. It was unknown if an autopsy was done. The cause of death was reported as Respiratory arrest. Company comment: Sanofi company comment on 16Dec2022. This case involved 67 years female patient who went out walking, collapsed, eyes rolled back and stopped breathing after receiving vaccines Pfizer biontech Covid-19 vaccine and influenza quadrival A-B high dose vaccine [Fluzone high dose quadrivalent]. This reported event stopped breathing was assessed as medically significant and fatal. Further information regarding medical history during vaccination, previously vaccination and tolerance, allergic history, laboratory investigations excluding alternative etiologies for the reported event are needed to fully access this case. Based upon the reported information, the role of the individual suspect vaccine cannot be addressed. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.; Reported Cause(s) of Death: stopped breathing; eyes rolled back; out walking, collapsed

Weitere VAERSDATA-Felder

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

VAERS 2562362

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: NC
Alter: 70,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 03.11.2022
Beginn: 23.11.2022
Tage bis Beginn: 20,0
Dosis: 5
Route/Site: SYR / RA

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

Angiogram pulmonary abnormal Anticoagulant therapy Arthralgia Atelectasis Cardiac disorder Deep vein thrombosis Electrocardiogram T wave inversion Groin pain Intensive care Pleural effusion Pulmonary arterial hypertension Pulmonary embolism Ultrasound Doppler abnormal

Symptomtext

Began having right hip and groin pain on 11/23/22, admitted to Hospital on 1/2/23 with acute Pulmonary Embolism and acute Deep Vein Thrombosis in right popliteral and peroneal veins.leg. Admitted to ICU on 1/2/23, Heparin administered and released on 1/6/23 with Eliquis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 5,0
Labordaten: EKG- new inverted T wave in V4. CTA chest pulmomary embolism bilateral multi lobar/multi segmental near occlusive pulmonary embolism with evidence of acute geart strain and pulmonary artery hyperter. Basilar atelectasis and small effusion Utrasound of right leg
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure, on meds
Andere Medikamente: Pantoprazole 40mg tablet Losarten hydrochorirthiazide 100-12.5 per tablet Tylenol Arthritis Pain oral Glucocamine Chrondroit oral
Allergien: penicillin Aleve (NASIDS) Codiene
Vorherige Impfungen: -

VAERS 2560742

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: WI
Alter: 79,0
Geschlecht: M
Eingang: 16.01.2023
Impfdatum: 04.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 4,0
Dosis: 5
Route/Site: IM / LA

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

Death No adverse event

Symptomtext

No adverse reaction was reported to local health department by client and/or family. Health Department received death report that client died of natural causes on 11/8/2022 at 1655. No autopsy was performed per death report and client has history of tobacco use, COPD, and Hypertensive and Atherosclerotic Cardiovascular Disease. Due to client receiving bivalent booster on 11/04/2022 VAERS is being completed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: COPD, Hypertensive and Atherosclerotic Cardiovascular Disease per death report.
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2554712

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: MI
Alter: 89,0
Geschlecht: F
Eingang: 09.01.2023
Impfdatum: 08.11.2022
Beginn: 02.01.2023
Tage bis Beginn: 55,0
Dosis: 4
Route/Site: IM / -

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

Acute respiratory failure COVID-19 Death General physical health deterioration Pneumonitis aspiration Respiratory failure SARS-CoV-2 test positive Tachypnoea

Symptomtext

COVID+ 1/2/23. Vaccination Status - moderna x4 + Pfizer BIVALENT x1 BRIEF OVERVIEW: Discharge Provider: MD, MPH Primary Care Physician at Discharge: DO Admission Date: 1/2/2023 Active Hospital Problems Diagnosis Date Noted POA ? COVID-19 virus infection 01/03/2023 Unknown ? Tachypnea 01/02/2023 Yes ? COVID-19 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Tachypnea Acute respiratory failure, unspecified whether with hypoxia or hypercapnia COVID-19 virus infection HOSPITAL COURSE: 89-year-old woman recently admitted for hypoxic and hypercapnic respiratory failure secondary to aspiration pneumonitis. She completed aspiration coverage with Unasyn and was weaned back to her baseline 2 L of oxygen and discharged to her facility. She came back COVID 19 positive with worsening respiratory failure and family elected to make patient comfort care / hospice. Family did not want to pursue aggressive measures and opted for comfort measures. Spectrum Health hospice was consulted and managing patient's symptoms. Due to decline in patient's clinical condition, she was made GIP Hospice and Hospice team helped manage patient's symptoms. Patient eventually passes away. Patient's son was at bedside when patient passed away. Medical Examiner Case Assessment Select Applicable Patient Criteria: Does not meet any of the listed criteria

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Problems from outside sources need reconciliation. Dysphagia Asthma Essential hypertension, benign Seasonal allergies Hypothyroidism, unspecified type Degeneration of lumbar intervertebral disc Osteoarthrosis involving lower leg Memory impairment Hyperlipidemia Continuous leakage of urine Dementia without behavioral disturbance, unspecified dementia type Fall Fall at home, initial encounter Acute respiratory failure with hypoxia Right lower lobe pneumonia
Andere Medikamente: Acetaminophen 1,000 mg Oral 3 times daily, For pain in right hip Albuterol Sulfate 108 (90 Base) MCG/ACT 2 puffs Inhalation Every 6 hours PRN Bisacodyl 10 mg Rectal Daily PRN Diclofenac Sodium 1 % Topical 2 times daily PRN, To the right hi
Allergien: 12 Hour Nasal Spray [Nasal Spray] FentanylThroat swelling Ketorolac Tromethamine [Toradol] Nsaids Penicillins
Vorherige Impfungen: -

VAERS 2549516

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

kritisch

Staat: WA
Alter: 70,0
Geschlecht: M
Eingang: 04.01.2023
Impfdatum: 29.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Cerebrovascular accident Fall

Symptomtext

Fell in parking lot, stroke

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: UTI
Vorgeschichte: -
Andere Medikamente: lisinopril, metroprolol, aspirin,
Allergien: -
Vorherige Impfungen: -

VAERS 2536674

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: WI
Alter: 90,0
Geschlecht: M
Eingang: 19.12.2022
Impfdatum: 19.12.2022
Beginn: 01.12.2022
Tage bis Beginn: -
Dosis: 5
Route/Site: IM / RA

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

Myocardial infarction

Symptomtext

Per client family, client had a heart attack (cardiac event) on 12/18/2022. Client hospitalized and being transitioned to hospice care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Client verbalized that he was diabetic. Client is also largely overweight at time of vaccination.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2536661

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: IL
Alter: 78,0
Geschlecht: F
Eingang: 19.12.2022
Impfdatum: 21.11.2022
Beginn: 13.12.2022
Tage bis Beginn: 22,0
Dosis: 4
Route/Site: IM / -

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

Acute kidney injury Death Myocardial infarction Rhabdomyolysis

Symptomtext

Health Department received a death certificate on this patient. Cause of Death 1. Myocardial Infarction 2. Acute Kidney Failure 3. Rhabdomyolysis . Health Department is filing a VAERS since this was only 22 days after vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Chronic Obstructive Pulmonary Disease
Vorgeschichte: COPD
Andere Medikamente: unk
Allergien: unk
Vorherige Impfungen: -

VAERS 2519967

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: WI
Alter: 66,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 14.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: SYR / RA

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

Cardiac arrest Cardioversion Catheterisation cardiac Computerised tomogram Implantable defibrillator insertion Magnetic resonance imaging Resuscitation Unresponsive to stimuli

Symptomtext

After vaccination on Oct. 14, without any warning signs, On Oct. 18 at 8 am I suffered cardiac arrest while still in bed. My husband called 911 and performed CPR. Paramedics shocked me 3 times, transported me to the hospital where I was again unresponsive and revived. I spent 9 days in the hospital. I was released Oct. 26 to go home. I have

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 9,0
Labordaten: Cardiac Catherization MRI CT scan insertion of pacemaker/ defibrillator
Aktuelle Erkrankungen: none
Vorgeschichte: obesity diabetes high blood pressure
Andere Medikamente: metformin calcium losartan simvastatin
Allergien: ACE inhibitors cause a cough
Vorherige Impfungen: -

VAERS 2500574

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

kritisch

Staat: SC
Alter: 66,0
Geschlecht: M
Eingang: 07.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Death Life support Resuscitation Unresponsive to stimuli

Symptomtext

Patient had dialysis on the morning of 11/4, received the covid vaccine and then went to a dermatologic office for a skin check. While he was getting checked he became unresponsive. CPR was started, patient came to the ER and ACLS care was given. Patient expired, Time of death was 13:17.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, CKD (requiring dialysis), Aortic valve stenosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2635598

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: OR
Alter: 24,0
Geschlecht: F
Eingang: 23.05.2023
Impfdatum: 23.05.2023
Beginn: 23.05.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Confusional state Dyskinesia Fear Hyperhidrosis Loss of consciousness Pallor

Symptomtext

Patient lost consciousness for 5 to 10 seconds, legs kicked and moved during unconscious state. Patient then came to and did not know where they were and stated was scared. Patient also appeared very pale sweating.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: N/A
Vorgeschichte: wheelchair bound (unknown condition to pharmacy)
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2624874

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: MI
Alter: 22,0
Geschlecht: M
Eingang: 02.05.2023
Impfdatum: 01.05.2023
Beginn: 01.05.2023
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

Patient fainted

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Called 911 Pt was evaluated and released at the scene
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2571732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

schwer

Staat: IN
Alter: 89,0
Geschlecht: M
Eingang: 31.01.2023
Impfdatum: 13.12.2022
Beginn: 17.12.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: OT / RA

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

Computerised tomogram Echocardiogram Investigation Pulmonary thrombosis X-ray

Symptomtext

blood clots in both lungs; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). An 89-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 13Dec2022 as dose 4 (booster), single (Lot number: GJ3275) at the age of 89 years intramuscular, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Blood pressure" (unspecified if ongoing). Concomitant medication(s) included: VALSARTAN oral taken for blood pressure abnormal. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Time: unknown, probably given in the morning. , Route of Administration: intramuscular; , Batch/Lot number: EL1283.), administration date: 16Jan2021, when the patient was 87-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE, Time: between 11:30 to 13:00., Anatomical location: Unknown arm., ROA: intramuscular;, Batch/Lot number: Unable to Locate or Read the Details;, Other, please specify: She says the first letter is hard to read, it could be an F or an E, then the rest is N6201. , The LOT number is handwritten on the vaccine card.), administration date: 13Feb2021, when the patient was 87-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Time: 16:30., Anatomical Site of injection: right arm., Route of Administration: intramuscular;, Batch/Lot number: LOT was handwritten caller says it looks like FE3590, it could be an E or a B then 3590, she can't tell.), administration date: 01Oct2021, when the patient was 87-year-old, for COVID-19 Immunization; Flu shot (flu shot in the second week of Oct2022, on Monday or Tuesday), administration date: Oct2022, for Immunization. The following information was reported: PULMONARY THROMBOSIS (hospitalization, medically significant) with onset 17Dec2022, outcome "recovered", described as "blood clots in both lungs". The patient was hospitalized for pulmonary thrombosis (start date: 17Dec2022, discharge date: 20Dec2022, hospitalization duration: 4 day(s)). The event "blood clots in both lungs" required emergency room visit. The patient underwent the following laboratory tests and procedures: Computerised tomogram: (unspecified date) Unknown Results; Echocardiogram: (unspecified date) heart was fine, it didn't do any damage; Blood clots: (17Dec2022) his blood clots were on the right side lung, notes: and affected right side heart; X-ray: (unspecified date) Unknown Results. Therapeutic measures were taken as a result of pulmonary thrombosis. Clinical course: Other concomitant medicinal product name as reported by the primary source: Water Pill. Consumer called for her husband for the Pfizer bivalent GJ3275 booster (injected intramuscularly into his right upper arm). On 13Dec2022 patient received this vaccine, then on 17Dec2022 he had blood clots in both lungs then had a procedure, interventional radiology, which saved his life. The blood clots were three days after he got that vaccine. They consulted four, clarified to three, different doctors: a GP, an interventional radiologist, and a hematologist. They feel like they do, that it is a contributing cause of blood clots, as he had had no symptoms. Patient was a 89 year old man, that was active and golfs everyday. He went to get the mail or newspaper and raised up and it hit him. They got him to the hospital and the emergency room did what they needed to do to find out what was wrong, which was blood clots to the top of both lungs. They took him from that hospital to the bigger hospital and the interventional radiologist got every one of them out. Patient had a handwritten vaccine card, he had this dose done at (facility name). NDC: not provided, initially provides LOT as GJ3275. EXP: not provided. The bivalent booster was his fourth dose. Indication: It was the booster that just came out, it was given around lunch time, noon. The flu vaccine and the Pfizer bivalent booster were given in the right arm, not at the same time, but this is consistent with what doctors said too, that his blood clots were on the right side lung and affected right side heart. They did an echocardiogram and his heart was fine, it didn't do any damage. Patient didn't do flu and COVID vaccines at the same time. They did a x-ray and a CT scan, and had the emergency room take him by ambulance to the larger hospital that had facilities to take care of him. They knew he had blood clots, and the doctor there was ready to receive him to do interventional radiology to remove them. The doctors said again today that they saved his life. Patient has recovered from the blood clots. but now he took Eliquis 5mg a day, clarified to twice a day, and he is under the care of a hematologist for that. He took the Eliquis 12 hours apart. Eliquis Manufacturer and it has Pfizer's name on it too. Patient got the flu shot at the same time, then later clarified he had his flu shot in the second week of Oct2022, on Monday or Tuesday. Consumer had no idea who manufacturer was, what the name of the flu shot was, it was done at it was done at (name), so whichever one they were doing at the time was done and was what they got. unspecified Flu shot NDC/LOT/EXP: unknown. Consumer initially said no to being asked if there were any recent new or relevant medications the weeks prior to his blood clots, and she said he was on the same things he had been on. She later said he takes Valsartan for a blood pressure medicine, but right now he is only taking if his blood pressure is over 140 because he is on Eliquis. Prior to getting the booster he took 160mg. He also took a water pill and something for high cholesterol. No further details provided about the water pill or high cholesterol medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary thrombosis
Hospital-Tage: 4,0
Labordaten: Test Name: CT scan; Result Unstructured Data: Test Result:Unknown Results; Test Name: echocardiogram; Result Unstructured Data: Test Result:heart was fine, it didn't do any damage; Test Date: 20221217; Test Name: Blood clots; Result Unstructured Data: Test Result:his blood clots were on the right side lung; Comments: and affected right side heart; Test Name: x-ray; Result Unstructured Data: Test Result:Unknown Results
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure abnormal
Andere Medikamente: VALSARTAN
Allergien: -
Vorherige Impfungen: -

VAERS 2560319

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: KS
Alter: 31,0
Geschlecht: M
Eingang: 15.01.2023
Impfdatum: 21.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 9,0
Dosis: 4
Route/Site: SYR / LA

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

Blood test Chest X-ray Computerised tomogram head Laboratory test Seizure

Symptomtext

SEIZURE at day service lasting 2-3 minutes, ambulance ride to hospital, much testing, sent home with directions to follow up with neurologist

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: ct scan head , chest xray, blood tests
Aktuelle Erkrankungen: NO
Vorgeschichte: HEMI CHOREA RIGHT ARM SHOWED UP SUDDENLY FALL 2020, autism since childhood
Andere Medikamente: OLANZAPINE, QUETIAPINE
Allergien: ERYTHROMYCIN
Vorherige Impfungen: -

VAERS 2548160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

schwer

Staat: KY
Alter: 12,0
Geschlecht: F
Eingang: 02.01.2023
Impfdatum: 10.12.2022
Beginn: 10.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Anaphylactic reaction Syncope

Symptomtext

upon receiving the updated bivalent pfizer covid 19 vaccine, the patient fainted and began to display signs and symptoms of anaphylaxis. she was there with her parents, and was helped to the floor so she was not injured from a fall. A technician yelled for the pharmacist on duty who administered epinephrine while 911 was called. the pharmacist stayed with patient monitoring symptoms until an ambulance arrived. She was taken to the emergency room where she was treated for anaphylaxis. the pharmacist followed up the next day with the family when she picked up her er prescriptions and had appeared to have made a full recovery.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: CRYSELLE, CETIRIZINE 10MG
Allergien: PINE NUTS
Vorherige Impfungen: -

VAERS 2537049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

schwer

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 14.10.2022
Beginn: 17.10.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: - / LA

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

Dry skin Electric shock sensation Full blood count Glycosylated haemoglobin Heart rate increased Heart rate Loss of personal independence in daily activities Muscle spasms Impaired work ability Laboratory test Metabolic function test Middle insomnia Muscle twitching Nervous system disorder Palpitations Rash Rash macular Sensory disturbance

Symptomtext

issues with my nervous system; My heart rate was elevated to 100 bpm; wake up with my heart racing; These mostly felt like vibrations; hands trembling,I felt internal tremors; I also felt "electric zaps" in parts of my body (groin and chest).; muscle spasms in my arms; Symptoms affected my ability to work; a huge rash on the left side of my torso at exactly the two-week point; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Oct2022 as dose 4 (booster), single (Lot number: GJ3275) at the age of 42 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "GERD" (unspecified if ongoing); "Known allergies: Sulpha" (unspecified if ongoing). Concomitant medication(s) included: OMEPRAZOLE. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 Immunization; Covid-19 vaccine (Dose 3 (BOOSTER), SINGLE Manufacturer Unknown), for COVID-19 Immunization. The following information was reported: ELECTRIC SHOCK SENSATION (non-serious) with onset 17Oct2022, outcome "recovering", described as "I also felt "electric zaps" in parts of my body (groin and chest)."; HEART RATE INCREASED (medically significant) with onset 17Oct2022, outcome "recovering", described as "My heart rate was elevated to 100 bpm"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious) with onset 17Oct2022, outcome "recovering", described as "Symptoms affected my ability to work"; VIBRATION SYNDROME (non-serious) with onset 17Oct2022, outcome "recovering", described as "These mostly felt like vibrations"; RASH (non-serious) with onset 17Oct2022, outcome "recovering", described as "a huge rash on the left side of my torso at exactly the two-week point"; TREMOR (non-serious) with onset 17Oct2022, outcome "recovering", described as "hands trembling,I felt internal tremors"; NERVOUS SYSTEM DISORDER (medically significant) with onset 17Oct2022, outcome "recovering", described as "issues with my nervous system"; MUSCLE SPASMS (non-serious) with onset 17Oct2022, outcome "recovering", described as "muscle spasms in my arms"; PALPITATIONS (medically significant) with onset 17Oct2022, outcome "recovering", described as "wake up with my heart racing". The events "issues with my nervous system", "my heart rate was elevated to 100 bpm", "wake up with my heart racing", "these mostly felt like vibrations", "hands trembling,i felt internal tremors", "i also felt "electric zaps" in parts of my body (groin and chest).", "muscle spasms in my arms", "symptoms affected my ability to work" and "a huge rash on the left side of my torso at exactly the two-week point" required physician office visit. The patient underwent the following laboratory tests and procedures: Heart rate: (17Oct2022) 100 bpm, notes: elevated. Therapeutic measures were not taken as a result of nervous system disorder, heart rate increased, palpitations, vibration syndrome, tremor, electric shock sensation, muscle spasms, loss of personal independence in daily activities, rash. Clinical course: The patient did not receive other vaccine in four weeks. The patient did not have covid prior to vaccination. The patient was not tested to covid post vaccination. She received the vaccine on Friday in the early afternoon. On Monday, she started experiencing issues with her nervous system. The patient felt internal tremors, which were mostly invisible to outsiders. These mostly felt like vibrations (like standing next to a washing machine), but sometimes it felt more like waves (like the patient was laying on a waterbed). Only occasionally others could see her hands trembling. She also felt "electric zaps" in parts of her body (groin and chest). The patient experienced muscle spasms in her arms as well where we could see her forearm flexing despite, she is being in a restful state. Her heart rate was elevated to 100 bpm for 5-6 weeks, and she would occasionally wake up with her heart racing. Symptoms affected her ability to work and lasted 5-6 weeks before they started to get better. She also broke out with a huge rash on the left side of her torso at exactly the two-week point. Symptoms have mostly subsided, but she still has the occasional racing heart and internal vibrations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Test Date: 20221017; Test Name: Heart rate; Result Unstructured Data: Test Result:100 bpm; Comments: elevated
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: GERD; Sulfonamide allergy
Andere Medikamente: OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2537049

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 14.10.2022
Beginn: 17.10.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: SYR / LA

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

Dry skin Electric shock sensation Full blood count Glycosylated haemoglobin Heart rate increased Heart rate Loss of personal independence in daily activities Muscle spasms Impaired work ability Laboratory test Metabolic function test Middle insomnia Muscle twitching Nervous system disorder Palpitations Rash Rash macular Sensory disturbance

Symptomtext

issues with my nervous system; My heart rate was elevated to 100 bpm; wake up with my heart racing; These mostly felt like vibrations; hands trembling,I felt internal tremors; I also felt "electric zaps" in parts of my body (groin and chest).; muscle spasms in my arms; Symptoms affected my ability to work; a huge rash on the left side of my torso at exactly the two-week point; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Oct2022 as dose 4 (booster), single (Lot number: GJ3275) at the age of 42 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "GERD" (unspecified if ongoing); "Known allergies: Sulpha" (unspecified if ongoing). Concomitant medication(s) included: OMEPRAZOLE. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 Immunization; Covid-19 vaccine (Dose 3 (BOOSTER), SINGLE Manufacturer Unknown), for COVID-19 Immunization. The following information was reported: ELECTRIC SHOCK SENSATION (non-serious) with onset 17Oct2022, outcome "recovering", described as "I also felt "electric zaps" in parts of my body (groin and chest)."; HEART RATE INCREASED (medically significant) with onset 17Oct2022, outcome "recovering", described as "My heart rate was elevated to 100 bpm"; LOSS OF PERSONAL INDEPENDENCE IN DAILY ACTIVITIES (non-serious) with onset 17Oct2022, outcome "recovering", described as "Symptoms affected my ability to work"; VIBRATION SYNDROME (non-serious) with onset 17Oct2022, outcome "recovering", described as "These mostly felt like vibrations"; RASH (non-serious) with onset 17Oct2022, outcome "recovering", described as "a huge rash on the left side of my torso at exactly the two-week point"; TREMOR (non-serious) with onset 17Oct2022, outcome "recovering", described as "hands trembling,I felt internal tremors"; NERVOUS SYSTEM DISORDER (medically significant) with onset 17Oct2022, outcome "recovering", described as "issues with my nervous system"; MUSCLE SPASMS (non-serious) with onset 17Oct2022, outcome "recovering", described as "muscle spasms in my arms"; PALPITATIONS (medically significant) with onset 17Oct2022, outcome "recovering", described as "wake up with my heart racing". The events "issues with my nervous system", "my heart rate was elevated to 100 bpm", "wake up with my heart racing", "these mostly felt like vibrations", "hands trembling,i felt internal tremors", "i also felt "electric zaps" in parts of my body (groin and chest).", "muscle spasms in my arms", "symptoms affected my ability to work" and "a huge rash on the left side of my torso at exactly the two-week point" required physician office visit. The patient underwent the following laboratory tests and procedures: Heart rate: (17Oct2022) 100 bpm, notes: elevated. Therapeutic measures were not taken as a result of nervous system disorder, heart rate increased, palpitations, vibration syndrome, tremor, electric shock sensation, muscle spasms, loss of personal independence in daily activities, rash. Clinical course: The patient did not receive other vaccine in four weeks. The patient did not have covid prior to vaccination. The patient was not tested to covid post vaccination. She received the vaccine on Friday in the early afternoon. On Monday, she started experiencing issues with her nervous system. The patient felt internal tremors, which were mostly invisible to outsiders. These mostly felt like vibrations (like standing next to a washing machine), but sometimes it felt more like waves (like the patient was laying on a waterbed). Only occasionally others could see her hands trembling. She also felt "electric zaps" in parts of her body (groin and chest). The patient experienced muscle spasms in her arms as well where we could see her forearm flexing despite, she is being in a restful state. Her heart rate was elevated to 100 bpm for 5-6 weeks, and she would occasionally wake up with her heart racing. Symptoms affected her ability to work and lasted 5-6 weeks before they started to get better. She also broke out with a huge rash on the left side of her torso at exactly the two-week point. Symptoms have mostly subsided, but she still has the occasional racing heart and internal vibrations.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: Test Date: 20221017; Test Name: Heart rate; Result Unstructured Data: Test Result:100 bpm; Comments: elevated
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: GERD; Sulfonamide allergy
Andere Medikamente: OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2530666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

schwer

Staat: CO
Alter: 16,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 13.12.2022
Beginn: 13.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Injection site pain Loss of consciousness Pallor Syncope

Symptomtext

Patient felt dizzy after getting Flucelvax shot since it "hurt". Waited a minute and then gave COVID booster when patient was ready. Patient began to feel more lightheaded and turned pale. Patient fainted and had difficulty coming to. Pharmacy Intern got the pharmacist for help and called 911. Patient was moved to the floor. Paramedics arrived and took over the situation. Patient was transported out on a stretcher but was alert and oriented.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2528996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

schwer

Staat: NJ
Alter: 18,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 09.12.2022
Beginn: 12.12.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

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

Loss of consciousness Syncope

Symptomtext

pt fainted about 5 minutes after receiving the 2 shots. She was sitting down in the waiting area and passed out for a very short period of time (seconds) . We called 911. Asked Pt to lie down afterwards with her legs elevated. EMS told us via phone to place her on her left side . EMS took pt with them.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2522456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 30.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

AFTER RECEIVING 2ND SHOT FOR FLU VACCINE, PATIENT STARTED TO PASS OUT. THEN QUICKLY CAME BACK AFTER CONTINUING CALLING OUT PATIENT. SHE DID NOT EAT ANYTHING BEFORE VACCINATIONS AND HAD FAINTED BEFORE. PHARMACY CALLED PARAMEDICS TO FOLLOW UP ON PATIENT BEFORE LEAVING THE PHARMACY. PATIENT WAS GIVEN ORANGE JUICE AND CRACKERS AFTER AWAKENING AND BEFORE PARAMEDICS ARRIVED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: NOT SPECIFY BY PATIENT
Vorgeschichte: NONE
Andere Medikamente: NO
Allergien: NO
Vorherige Impfungen: -

VAERS 2512848

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

schwer

Staat: UT
Alter: 23,0
Geschlecht: M
Eingang: 21.11.2022
Impfdatum: 21.11.2022
Beginn: 21.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Head injury Loss of consciousness

Symptomtext

Patient received both vaccines and upon getting up to leave he passed out and hit his head. Ambulance was called. Paramedics assessed the patient and released him

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2510455

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: OK
Alter: 28,0
Geschlecht: M
Eingang: 17.11.2022
Impfdatum: 12.11.2022
Beginn: 12.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Feeling hot Flushing Hyperhidrosis Hypotension Syncope Vomiting

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Systemic: Vomiting-Medium, Additional Details: Patient was exhibiting symptoms of syncope: sweatiness, hot, dizziness, and also vomited. BP was 111/62 HR 65. We have her water and monitored for an additional 10 minutes. She felt better after throwing up and drinking water. She also received her flu vaccine that day.

Weitere VAERSDATA-Felder

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

VAERS 2507560

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

schwer

Staat: CA
Alter: 90,0
Geschlecht: M
Eingang: 14.11.2022
Impfdatum: 14.11.2022
Beginn: 14.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

General physical condition abnormal Syncope

Symptomtext

Patient received the Pfizer COVID booster and then the high dose senior flu shot. After getting the flu vaccine, the patient looked off but insisted that he was fine. After taking a few steps out the vaccination room, he collapsed. Patient was offered water and EMS was contacted. EMS offered to take him to the ER but patient refused. Pharmacy staffed called and left message at 1500 to check on the status of the patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2506170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: MD
Alter: 25,0
Geschlecht: M
Eingang: 11.11.2022
Impfdatum: 11.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Electric shock sensation Pain Pain in extremity

Symptomtext

patient requested to have fluarix in right arm and pfizer bivalent in left arm. patient reported "electric pain" shooting down in left lower calf when his foot touches the floor while walking 30 minutes after administration.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2504050

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: WA
Alter: 13,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 09.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Hunger Syncope Visual impairment

Symptomtext

Approximately 10 minutes after receiving her vaccines, patient's vision went dark and she fainted. Was roused immediately and felt fine after having some orange soda. After speaking to mom, patient had not eaten since an early breakfast. Pt was able to stand without any lightheadedness after a couple of minutes of being told to sit and drink her soda. She said she was hungry and she and mom left to get food.

Weitere VAERSDATA-Felder

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

VAERS 2502779

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

schwer

Staat: OR
Alter: 42,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 01.11.2022
Beginn: 01.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / LA

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

Asthenia Heart rate Heart rate increased Muscle fatigue Syncope Vomiting

Symptomtext

2 episodes of sycope; 2 episodes of vomiting; extreme muscle fatigue; weakness; fast heartbeat; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 01Nov2022 as dose 4 (booster), single (Lot number: GJ3275) at the age of 42 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "POTS syndrome" (unspecified if ongoing). Concomitant medication(s) included: ZYRTEC [CETIRIZINE HYDROCHLORIDE]. Vaccination history included: Covid-19 vaccine (DOSE 2, SINGLE, Lot number: Not reported), for Covid-19 immunization; Covid-19 vaccine (DOSE 3 (BOOSTER), SINGLE, Lot number: Not reported), for Covid-19 immunization; Covid-19 vaccine (DOSE 1, SINGLE, Lot number: Not reported), for Covid-19 immunization. The following information was reported: SYNCOPE (medically significant) with onset 01Nov2022, outcome "unknown", described as "2 episodes of sycope"; VOMITING (non-serious) with onset 01Nov2022, outcome "unknown", described as "2 episodes of vomiting"; MUSCLE FATIGUE (non-serious) with onset 01Nov2022, outcome "unknown", described as "extreme muscle fatigue"; HEART RATE INCREASED (non-serious) with onset 01Nov2022, outcome "unknown", described as "fast heartbeat"; ASTHENIA (non-serious) with onset 01Nov2022, outcome "unknown", described as "weakness". The patient underwent the following laboratory tests and procedures: Heart rate: (01Nov2022) Fast. Therapeutic measures were not taken as a result of syncope, vomiting, muscle fatigue, asthenia, heart rate increased. Clinical course: other medications in two weeks: Zyrtec, vitamins. 2 episodes of syncope, 2 episodes of vomiting, extreme muscle fatigue, weakness, and fast heartbeat on 01Nov2022. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Test Date: 20221101; Test Name: Heartbeat; Result Unstructured Data: Test Result:Fast
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Postural orthostatic tachycardia syndrome
Andere Medikamente: ZYRTEC [CETIRIZINE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2499987

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 05.11.2022
Impfdatum: 05.11.2022
Beginn: 05.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Syncope

Symptomtext

I personally didn't witness the event, but a coworker reported that patient fainted after getting vaccine. Patient was shopping the store after receiving vaccine and while shopping, patient fainted. I was told after couple minutes, patient was feeling fine and continued with her shopping.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Unsure
Vorgeschichte: Heart, liver, and diabetes chronic conditions reported on immunization intake form
Andere Medikamente: Unsure
Allergien: Penicillin - rash; paper tape - rash
Vorherige Impfungen: -

VAERS 2497833

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: OH
Alter: 24,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 03.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Loss of consciousness

Symptomtext

passed out after 2nd shot was given and began to have a possible seizure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2497767

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: MA
Alter: 38,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 03.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia Dizziness Immediate post-injection reaction Incontinence Seizure Unresponsive to stimuli

Symptomtext

Pt was given her Covid Booster and immediately became weak, dizzy and unresponsive Pt was unresponsive to sternal rub. No rhythmic body movements, incontinence, other sx of seizure activity. After a few minutes, pt began moving eyes somewhat and was able to blink on command. Not able to follow any other commands. 911 called, EMS arrived to transport pt to hospital to r/o seizure. Thought to be less likely vagal response to inj given normal HR and BP while unresponsive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Funtional neurological disorder
Andere Medikamente: pyridostigmine (MESTINON) 60 mg/5 mL syrup [] Order Details Dose: 15 mg Route: Oral Frequency: 3 times daily Dispense Quantity: 200 mL Refills: 0
Allergien: NKA
Vorherige Impfungen: -

VAERS 2495981

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

schwer

Staat: OH
Alter: 17,0
Geschlecht: M
Eingang: 02.11.2022
Impfdatum: 29.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Disorientation Dizziness Fall Loss of consciousness Skin abrasion Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Additional Details: After receiving the covid vaccine the patient lost consciousness for a moment causing him to fall out of his chair. Patient was dissoriented for a few minutes following the fainting spell. He did sustain minor abrasions to his face resulting from the fall. He seemed to fully recover after having some gatorade and crackers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2492278

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: CA
Alter: 22,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 23.10.2022
Beginn: 23.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Fall Seizure Syncope Tremor Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Systemic: Seizure-Mild, Systemic: Shakiness-Mild, Additional Details: Patient came in to receive both the seasonal flu vaccine and the pfizer bivalent booster. seconds later she feld lightheaded and then she slid down the chair and had a seizure. parametics were called and she was evaluated. they recommended she go with them but she refused.

Weitere VAERSDATA-Felder

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

VAERS 2492267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: TX
Alter: 25,0
Geschlecht: M
Eingang: 28.10.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Fall Pallor Syncope

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Additional Details: PT HAD BOTH VACCINES THEN COMMENTED THAT EASY THEN 5 SECONDS LATER FAINTED. HE THEN WOKE UP, 5 SECS LATER WITH NO IDEA OF HOW HE ENDED UP ON FLOOR. HE APPEARED PALE AND STAYED FOR 30 MINS AND SAID HE FELT FINE AND LEFT.

Weitere VAERSDATA-Felder

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

VAERS 2491382

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

schwer

Staat: MD
Alter: 39,0
Geschlecht: M
Eingang: 27.10.2022
Impfdatum: 26.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Feeling cold Immediate post-injection reaction Nausea Pallor Paraesthesia Syncope

Symptomtext

Syncope immediately after second vaccine was delivered. After regaining consciousness, he was unable to move for about another 5 seconds and was blanched, cold, and nauseous for several hours after. Tingling in extremities on the drive home, and nearly fainted again. Tingling in extremities still occurring during driving 19 hours later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: idiopathic urticaria
Vorgeschichte: idiopathic urticaria
Andere Medikamente: cetirizene, multivitamin
Allergien: idiopathic urticaria
Vorherige Impfungen: -

VAERS 2488180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

schwer

Staat: CA
Alter: 17,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia Hypotension Syncope Tinnitus

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Systemic: Tinnitus-Mild, Systemic: Weakness-Mild, Additional Details: Patient fainted after medication administration. blood pressure was taken and was low. patient drank some water and remained laying down until she felt better. elevated her legs to keep help with her blood pressure. Patient was fine after about 20 minutes

Weitere VAERSDATA-Felder

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

VAERS 2641120

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 05.06.2023
Impfdatum: 03.11.2022
Beginn: 15.05.2023
Tage bis Beginn: 193,0
Dosis: 5
Route/Site: - / -

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

Angiogram pulmonary abnormal Asthenia COVID-19 Chest X-ray abnormal Chills Computerised tomogram head normal Computerised tomogram spine Cystitis Diarrhoea Dyspnoea Fatigue Pneumonia Pulmonary mass SARS-CoV-2 test positive Urinary tract infection Urine analysis abnormal White blood cell count increased

Symptomtext

5/15/2023 - 5/18/2023 (3 days) DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: UTI (urinary tract infection) Weakness Acute cystitis without hematuria Pneumonia of right upper lobe due to infectious organism COVID-19 HOSPITAL COURSE: Patient is a 71 y.o. female with PMH of GERD, GAD, HLA b27 spondyloarthropathy and ho presents today with cc of sob. She reports she has been having sob accompanied w chills since Saturday. Has also been feleing weak and fatigued. In ED pts VS stable. Pertinent labs include: elevated wbc count, positive UA. Chest xray showing RUL pna. CT head, C-spine were unremarkable for any sign of acute traumatic process. COVID was positive. CTA was obtained which does show a 7 mm pulmonary nodule which is recommended to have follow-up in 6 months. The patient was on room air throughout her stay. No steroids or remdesivir were initiated. Patient was treated for urinary tract infection as well as pneumonia. On discharge she was switched to levofloxacin to complete a 5 day course for the pneumonia. During her hospital stay the patient did report having diarrhea after antibiotic administration, however that resolved prior to discharge. The patient was feeling much better than when she 1st came in and she was instructed follow up with her primary care doctor for further monitoring. The patient was discharged in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Cholelithiasis Liposarcoma, low grade, left leg OA (osteoarthritis) of the hips Liver fibrosis - hepatitis Dense breasts Gastroesophageal reflux disease without esophagitis Invasive ductal carcinoma of breast, stage 2, right GAD (generalized anxiety disorder) Inflammatory arthritis Status post bilateral knee replacements HLA-B27 spondyloarthropathy Primary osteoarthritis involving multiple joints Prophylactic use of tamoxifen Controlled substance agreement signed Osteopenia of multiple sites Long term systemic steroid user Long-term use of Plaquenil HTN, goal below 130/80
Andere Medikamente: acetaminophen (TYLENOL) 500 mg tablet alendronate (FOSAMAX) 70 MG tablet cholecalciferol (VITAMIN D3) 25 MCG (1000 UT) tablet citalopram (CELEXA) 40 MG tablet famotidine (PEPCID) 20 mg tablet folic acid (FOLVITE) 1 MG tablet gabapentin (NEU
Allergien: Cefaclor CrRash CephalosporinsRash PenicillinsRash
Vorherige Impfungen: -

VAERS 2632996

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: WI
Alter: 59,0
Geschlecht: F
Eingang: 17.05.2023
Impfdatum: 15.11.2022
Beginn: 21.03.2023
Tage bis Beginn: 126,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Cough Discomfort Dyspnoea Fatigue Oropharyngeal pain SARS-CoV-2 test positive Sleep disorder

Symptomtext

On the morning of 3/21/2023, I noticed that I had a sore throat. The sore throat lasted for a couple of days, and on 3/22/2023, I started to also feel tired. In the early hours of 3/23/2023, I woke up with an extremely sore throat. At 2:30 AM, I took a lateral flow COVID-19 test and got a positive result. On 3/23/2023, I had a telehealth visit with my doctor, who prescribed me Paxlovid. She also told me that I could take OTC medicines like Advil and Tylenol to manage discomfort. I began taking the Paxlovid on 3/24/2023. I soon started to feel better afterwards, though I continued to test positive. On 3/28/2023, I finished the Paxlovid. On 3/29/2023, I tested negative for COVID-19. After all of that, I continued to have issues with breathing and coughing for about three weeks afterwards. I ended up using my inhaler about two or three times during this period.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 23MAR2023 - Lateral Flow COVID-19 Test - Positive Result; 29MAR2023 - Lateral Flow COVID-19 Test - Negative Result
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma; Hormonal Imbalance
Andere Medikamente: Progesterone (Oral); Estriol Vaginal Cream; E2, E3, Progesterone, and Testosterone Compounded Topical Cream; Vitamin D3; Vitamin K2; Magnesium Carbonate; Ventolin HFA Inhaler
Allergien: Gluten
Vorherige Impfungen: -

VAERS 2627388

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: OR
Alter: 68,0
Geschlecht: M
Eingang: 05.05.2023
Impfdatum: 12.10.2022
Beginn: 08.04.2023
Tage bis Beginn: 178,0
Dosis: 5
Route/Site: IM / LA

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

Bronchitis COVID-19 Fatigue Hypersensitivity Pneumonia Respiratory disorder SARS-CoV-2 test positive

Symptomtext

Prior to having COVID-19 infection, I had three weeks of respiratory illness that lingered and became complicated with allergies. After three weeks of the respiratory illness, it moved to Bronchitis and Pneumonia. I was prescribed an antibiotic, erythromycin. At this time, I was testing negative for COVID-19. 2 days after taking the antibiotic, on 04/08/2023, I tested positive for COVID-19 with home test. I was prescribed PAXLOVID on 04/08/2023. I never really experienced any significant COVID-19 symptoms other than fatigue. Just the symptoms that I was already experiencing with the respiratory illness. After taking the PAXLOVID for 5 days I tested negative on 04/14/2023 and I was feeling pretty good. I have been healthy ever since.

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Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: 08APR2023 COVID-19 home test positive; 14APR2023 COVID-19 home test negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2626590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: WA
Alter: 72,0
Geschlecht: M
Eingang: 04.05.2023
Impfdatum: 29.11.2022
Beginn: 01.12.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / UN

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

Atrial fibrillation Cardiac monitoring abnormal Cardiac stress test normal Echocardiogram normal Palpitations

Symptomtext

In December 2022 I was having a racing heart rate for no reason. My normal is 65 and it would be 105 or higher. It would remain consistent for several days. I visited the doctor on December 14th and wore a heart monitor for two weeks. I learned I was in AFIB about 25 percent of the time. I consulted further and will probably have an ablation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Echocardiogram, normal, 12/2023; Cardiac Stress test, normal, 12/2023
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Cholesterol; Hypertension
Andere Medikamente: Atorvastatin; hydrochlorothiazide; vitamin D
Allergien: Penicillin; dust mites
Vorherige Impfungen: -

VAERS 2624000

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: WA
Alter: 77,0
Geschlecht: F
Eingang: 01.05.2023
Impfdatum: 22.10.2022
Beginn: 01.01.2023
Tage bis Beginn: 71,0
Dosis: 5
Route/Site: IM / LA

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

Computerised tomogram Confusional state Dizziness Electrocardiogram normal Feeling abnormal Headache Magnetic resonance imaging Paraesthesia

Symptomtext

In April 2023 I had extreme dizziness and was able to walk well. I have also had odd headaches with intense sharp feelings that don't last very long, and this began in January 2023. I have also had facial tingling that started in about February 2023. I saw my doctor on April 10, 2023. The doctor referred me to a hospital. However, I ended up going to the emergency room on April 18, 2023. They ran tests and determined I did not have a stroke, clots or brain tumor. I will see my doctor again tomorrow. I see another doctor today, physical therapist, that specializes in vertigo. In addition, I have been experiencing growing confusion.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: MRI, unknown, 042023; CT Scan, unknown, 042023; EKG, normal, 042023
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Zyrtec
Allergien: Codeine; Flagelle
Vorherige Impfungen: -

VAERS 2623340

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: AZ
Alter: 67,0
Geschlecht: F
Eingang: 28.04.2023
Impfdatum: 23.10.2022
Beginn: 02.11.2022
Tage bis Beginn: 10,0
Dosis: 5
Route/Site: IM / LA

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

Asthenia Blood immunoglobulin G decreased COVID-19 Condition aggravated Fibromyalgia Full blood count normal Infection Laboratory test normal Pain Post-acute COVID-19 syndrome Pyrexia Quality of life decreased Red blood cell sedimentation rate normal SARS-CoV-2 test positive

Symptomtext

11/2/2022 body aches everywhere, 10/10 all over. Test positive on at home COVID-19 test. For the next week I had pain in my body everywhere, and fever. The fever broke after about a week, but pain continued until time of reporting with weakness. Rheumatologist states that all tests show normal and stated this is likely Long Covid but diagnosed Fibromyalgia and PCP prescribed gabapentin to treat Fibromyalgia. Quality of life has drastically reduced because of infection.

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 2Nov2022 at home COVID-19 test, positive, AVISE, CBC, Sed Rate test, only abnormality was IGG3 deficiency
Aktuelle Erkrankungen: Osteoarthritis; Hypothyroidism
Vorgeschichte: Fibromyalgia; Hypothyroidism; Osteoarthritis
Andere Medikamente: Levothyroxine; buspirone; trazodone; prazosin; lamotrigine; multivitamin
Allergien: TALWIN; latex
Vorherige Impfungen: After second shingles vaccine in March of 2023, I had fever, body aches and chills for 2 days. Shingrix Vaccine 68

VAERS 2623322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: AZ
Alter: 69,0
Geschlecht: F
Eingang: 28.04.2023
Impfdatum: 24.10.2022
Beginn: 01.12.2022
Tage bis Beginn: 38,0
Dosis: 4
Route/Site: IM / AR

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

Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Emphysema Fatigue Malaise Pneumonia Pyrexia

Symptomtext

It's ongoing since 12/2022, I have been feeling sick. I have had a fever on and off for the last three months. The doctor referred me an infectious disease specialist. I stopped seeing him because he said he could not help me anymore. A pulmonologist in March 2023, looked at my X-ray from December 20222 and diagnosed me with Pneumonia and put me on antibiotics and also told me I had Emphysema. My COPD had become worse. My pulmonologist ordered another chest X-ray I asked him to send it to my PCP. My PCP did not tell me I had pneumonia she put me on antibiotics because I was running a fever of 101 in her office. I have been on antibiotics 3 or 4 times. I do not know if I should go on them again. When I was driving to my pulmonologist appointment, I wasn't it feeling well. I cancelled my appointment. I have been feeling too tired to do anything. I lost confidence in my PCP for not telling me I had pneumonia. I am scheduled to get my lab work on 05/03/2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: DEC2022 - Chest X-ray -Unknown; MAR2023 - Chest X-ray - Pneumonia
Aktuelle Erkrankungen: N/A
Vorgeschichte: GOUT; COPD; Emphysema; Pneumonia
Andere Medikamente: D-Amphetamine Salt; Oxycodone-Acetaminophen; Relistor; Alopurinol; Metroprolol; Citalopram; Zyrtec; Mucous Relief; Stool Softener; Excedrin Migraine; Vitamin C; Calcium; Visbiome Probiotic; Vitamin D
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2622882

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ3275

moderat

Staat: MI
Alter: 62,0
Geschlecht: F
Eingang: 27.04.2023
Impfdatum: 31.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

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

Arthralgia Back pain Bladder spasm Condition aggravated Magnetic resonance imaging normal Pain Pelvic pain Ultrasound scan normal

Symptomtext

I had lower back pain, I had pain on my right hip and my pelvis area (in the joints). It could be muscle or nerve pain. My doctor sent me for a physical therapy, I did that for the whole month of Dec, after holidays, still hurting, I had physical therapy for 3 months and he did ultrasound on me, MRI. On dec 2nd I went to a Urologist for the Bladder Spasm and the gynecologist, radiology and primary doctor. Tomorrow I will have another MRI to see where the pain is.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: DEC2023 - MRI - Normal; 03MARCH2023 - Ultrasound - Normal
Aktuelle Erkrankungen: Bladder Spasm
Vorgeschichte: Arthritis: Bursitis
Andere Medikamente: Oxybutynin; Rosuvastatin; Vitamin D; Vitamin C; Zinc; Calcium; B12
Allergien: Sulfur
Vorherige Impfungen: -

VAERS 2622456

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: TX
Alter: 61,0
Geschlecht: F
Eingang: 27.04.2023
Impfdatum: 26.10.2022
Beginn: 10.02.2023
Tage bis Beginn: 107,0
Dosis: 4
Route/Site: IM / RA

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

Asthma Chest X-ray normal Condition aggravated Cough Dyspnoea Environmental exposure Pyrexia

Symptomtext

I have allergic asthma and I was cleaning an office and I had a dust exposure, I was then having a very hard cough, sore cough, and it was hard to breath and developed and fever. I was taking some OTC medication and after 12 days the cough was not going away. I went in and my doctor gave me an antibiotic and a steroid. We did do a chest x-ray to make sure I did not have pneumonia and that was ruled out as well and we really nailed down that it was my asthma that was the problem. When I went off that however it came back. I am now on the medication full time, and I was diagnosed with exacerbated asthma and have medications added to my daily medication routine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Chest X-ray;
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; Obesity; Asthma
Andere Medikamente: Atorvastatin; Metformin; Amlodipine; Vitamin A; Vitamin E
Allergien: N/A
Vorherige Impfungen: -

VAERS 2622305

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: TX
Alter: 57,0
Geschlecht: M
Eingang: 27.04.2023
Impfdatum: 26.10.2022
Beginn: 01.04.2023
Tage bis Beginn: 157,0
Dosis: 5
Route/Site: IM / AR

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

Dyspnoea Nasal congestion Productive cough Upper-airway cough syndrome

Symptomtext

I started noticing that during my daily walks I was becoming short of breath, this is not normal for me. I walk daily, I work out in the gym to stay healthy to keep my myself healthy and my lungs fit. I had nasal congestion so bad that I was going through a box of Kleenex a day, the drainage was also going down my throat, I was coughing it up. I made an appointment to see my doctor, I was not tested for any of the normal things, COVID-19, RSV, Influenza. I was given a steroid shot, and an antibiotic to take for three days. It took three weeks to get rid of major symptoms, but I am still battling the congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Multivitamin
Allergien: No
Vorherige Impfungen: -

VAERS 2620748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: CO
Alter: 69,0
Geschlecht: M
Eingang: 25.04.2023
Impfdatum: 22.10.2022
Beginn: 07.02.2023
Tage bis Beginn: 108,0
Dosis: 5
Route/Site: IM / AR

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

Atrial fibrillation Clumsiness Condition aggravated Electrocardiogram abnormal Gait disturbance Intracranial mass Magnetic resonance imaging head abnormal Mastoid effusion Memory impairment Road traffic accident Sinus disorder Visual acuity tests

Symptomtext

Midday on February 7, 2023, I lightly scraped the car to the right of me. On February 9, 2023, I had an episode of Atrial Fibrillation. It was my first episode since my initial episode on July 12, 2020. Then, on February 13, 2023, I was in a parking lot pulling out to leave, and I bumped into the rear bumper of another car. On February 13, 2023, I went back into Atrial Fibrillation while talking to the insurance agent about the accident. Each of those episodes were about 1.5 to 3 hours long. I saw my doctor on February 15, 2023. One thing we discovered was that my right eye, which had a near vison contact in it, was 2200 for far vision. In July of 2022, when I saw my eye doctor, my left eye was near vision and right eye was far vision. Throughout most of my life, I had distance vision in my left eye, and it was dominant. I asked if I could switch it back to have my dominant eye continue to be my dominant eye. He said my prescription would be pretty much the same for both eyes, so he suggested I wear my driving glasses upside down. I stopped wearing my driving glasses for short distances months before these accidents. What I've noticed since February, particularly in latter March and in April, is some increased clumsiness. I drop things and trip over things without dizziness, double vision, lightheadedness, or loss of strength. One episode was last week. It took me several tries to remember the last few digits of my own phone number. It doesn?t appear that poor right distance vision with a contact is a change. I have an appointment with an ENT on May 17, 2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 02/09/2023 EKG - Atrial Fibrillation Ventricular Response Rate 130-160; 02/15/2023 Visual Acuity - Left Eye distance vision with contact 20/30, Right Eye with near vision contact distance vision 20/200; 02/15/2023 Physical Exam - Normal; 03/01/2023 MRI of Brain without Contrast - Mass-like 1.8cm Thickening about the Posterior Inferior Sphenoid Sinus, could be related to Sinus Mucosal Disease such as a Mucosal Retention Cyst. Also, showed Right Mastoid Effusion.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Hypothyroidism; ADHD; ADHD Medication Induced Insomnia; Paroxysmal Atrial Fibrillation
Andere Medikamente: Bupropion; Amlodipine; Levothyroxine; Adderall; Trazadone; Vitamin D; Omega 3; Nature's Oasis Sleep; Night Rest; Testosterone
Allergien: Codeine; Latex; Seasonal: Raid
Vorherige Impfungen: -

VAERS 2620656

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge GJ3275

moderat

Staat: KS
Alter: 61,0
Geschlecht: F
Eingang: 25.04.2023
Impfdatum: 24.10.2022
Beginn: 05.02.2023
Tage bis Beginn: 104,0
Dosis: 4
Route/Site: IM / LA

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

Catheterisation cardiac normal Chest discomfort Dizziness Dyspnoea Fatigue Heart rate decreased Pain in jaw Palpitations

Symptomtext

On 02/05/2023, I woke up and my heart started racing really fast. I got pain in my jaw and chest discomfort, shortness of breath. I put an oximetry and the pulse was low as 27/100. It did this for ten minutes then it stopped. I went to work and a nurse at work told me to go to the ER. I usually have a low pulse. I went to ER but did not get treatment. On 04/11/2023, I was sitting in a meeting at work and my heart started beating really hard, they took my pulse and it was 122 and my blood pressure was 186/100 and I was sent to the ER. At the ER they did a heart catheter and they did not find any blockages. I am still having alot of fatigue and light headiness. They put me on blood pressure medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 11APR2023 Heart Catheter- showed no blockages
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia; Arthritis; Period of Rectal Bleeding
Andere Medikamente: Pantoprazole
Allergien: Dilantin; Erythromycin; Septran DS
Vorherige Impfungen: -

VAERS 2619328

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: NC
Alter: 23,0
Geschlecht: F
Eingang: 21.04.2023
Impfdatum: 21.04.2023
Beginn: 21.04.2023
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Blood pressure increased Chest discomfort Cold sweat Dyspnoea Electrocardiogram normal Hyperhidrosis Hypertension Tachycardia

Symptomtext

Within 15 minutes of vaccination, patient reported feeling sweaty, hands were clammy, and chest tightness and discomfort. She stated that her "heart felt inflamed." Patient was watched for 15 more minutes, at which point she was sweating more and having some labored breathing, but no difficulty speaking. EMS was called and she was found to be highly tachycardic and hypertensive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: ECG was normal sinus tachycardia, blood pressure was elevated substantially.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Collagen
Allergien: None
Vorherige Impfungen: -

VAERS 2614610

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: AZ
Alter: 70,0
Geschlecht: F
Eingang: 13.04.2023
Impfdatum: 03.11.2022
Beginn: 02.03.2023
Tage bis Beginn: 119,0
Dosis: 5
Route/Site: SYR / LA

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

Anticoagulant therapy Atrial fibrillation Chest X-ray abnormal Cough Electrocardiogram abnormal Malaise Nasopharyngitis Pneumonia Pyrexia Sepsis

Symptomtext

I had a bad cold that started in Christmas time and that never went away. It turned into pneumonia and I was septic and I was taken to the hospital in March. I was taken to an urgent care a day before that and I was prescribed antibiotics. I took one dose and became really sick during the night. Emergency help came and took me to the hospital. I had 104 fever and a bad cough. X-rays at the hospital showed the lungs were filled with pneumonia. The EKG showed that I had afib. I got new medications after being discharged from the hospital. It was benzonatate, metoprolol, and ELIQUIS. I also used an albuterol inhaler.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pneumonia
Hospital-Tage: 3,0
Labordaten: 02MAR2023 Chest X-ray, indicated lungs filled with pneumonia
Aktuelle Erkrankungen: CT scan of Abdomen for Flank Pain showed lymph nodes near the liver, kidney cysts, and twisted gallbladder October 2022
Vorgeschichte: High Cholesterol; Hypertension; Hypothyroidism; Left Bundle Branch Block; Urinary Incontinence; Chronic Pain
Andere Medikamente: Albuterol inhaler; amitriptyline; atorvastatin; gabapentin; levothyroxine; losartan; tamsulosin; tizanidine; tramadol; mupirocin topical ointment; triamcinolone acetonide; aspirin; biotin; COLACE; calcium CALTRATE; vitamin D3; vitamin B com
Allergien: None
Vorherige Impfungen: -

VAERS 2613890

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 09.11.2022
Beginn: 26.01.2023
Tage bis Beginn: 78,0
Dosis: 5
Route/Site: IM / LA

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

Arteriosclerosis Blood iron decreased Cardiac stress test normal Chest discomfort Echocardiogram normal Electrocardiogram abnormal Exercise tolerance decreased Heart rate increased Laboratory test Mobility decreased Palpitations Ventricular extrasystoles

Symptomtext

On January 26, 2023, I climbed the stairs and felt like my heart was beating out of my chest. I usually climb four flights of stairs at work, but I had to take the elevator the rest of the way. Prior to this, my smart watch showed my heart was jumping to the rate of 130 beats per minute while walking normally. My chest felt like funny, but it was not painful. I didn't feel like I was going to pass out either. On February 10, 2023, I saw my doctor. They did an EKG. They found some PVC. They ordered a 24-hour heart monitor and prescribed propranolol. They also took labs. They also performed a Heart Echo. There were no significant findings. I requested a Cardiac CT due to family history of heart attack. My labs showed low on iron, but everything else was normal. On March 16, 2023, I had the Cardiac CT. It showed Zero Coronary Calcium Score, but there was soft plaque. I also had a Stress Test on April 7, 2023. There was no evidence of Ischemia. I have a Cardiological Consultation on April 26, 2023. Since then, I am taking propranolol twice a day, atorvastatin once a day, and baby aspirin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 02/10/2023 EKG, PVC; 02/10/2022 Heart Monitor, no significant findings; 03/10/2023 Labs, low iron; 03/10/2023 Heart Echo, no significant findings; 03/16/2023 Cardiac CT, Coronary Calcium Score and Soft Plaque in the Proximal LAD; 04/07/2023 Stress test, no evidence of Ischemia
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines; Acid Reflux; Neck Pain; Stress from Work
Andere Medikamente: MAXALT; estradiol; vitamin D3
Allergien: Seasonal; sulfa drugs
Vorherige Impfungen: -

VAERS 2607353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

moderat

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 31.03.2023
Impfdatum: 31.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dysphonia Dyspnoea Fatigue Lethargy

Symptomtext

Systemic: Exhaustion / Lethargy-Medium, Systemic: Pt states that her voice became raspy, she's fatigued, shortness of breath, when laying on her back at night it's hard to breath-Medium, Additional Details: Patient is currently 18 weeks pregnant. She was told that some of these symptoms could be caused from the pregnancy. She said she was not pregnant at the time that symptoms arose. She currently does not have regular insurance, only the RX for pregnancy.

Weitere VAERSDATA-Felder

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

VAERS 2602353

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: MN
Alter: 78,0
Geschlecht: M
Eingang: 23.03.2023
Impfdatum: 31.10.2022
Beginn: 12.12.2022
Tage bis Beginn: 42,0
Dosis: 5
Route/Site: IM / RA

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

Asthenia COVID-19 Condition aggravated Diabetes mellitus Hyperglycaemia Illness Mental status changes Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient with history of dementia and diabetes. He was brought to the ED by EMS on 12/12/2022 for evaluation of weakness, fever of 103 F, and altered mental status. He tested positive for COVID prior to ED arrival, and again by PCR in the ED. Ultimately, patient admitted 12/12/22 - 12/28/22 for acute on chronic weakness in the setting of COVID illness. He was discharged to an assisted living facility. Notably, patient returned to the ED on 12/29/22 by EMS for hyperglycemia and again was admitted 12/29/22 - 1/20/23 for hyperglycemia due to diabetes.

Weitere VAERSDATA-Felder

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

VAERS 2596278

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: AZ
Alter: 70,0
Geschlecht: M
Eingang: 14.03.2023
Impfdatum: 10.12.2022
Beginn: 20.02.2023
Tage bis Beginn: 72,0
Dosis: 4
Route/Site: IM / RA

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

COVID-19 Chills Cough Fatigue Feeling abnormal Lacrimation increased Malaise Mobility decreased Myalgia Paranasal sinus discomfort Productive cough Pyrexia Rhinorrhoea SARS-CoV-2 test positive Secretion discharge

Symptomtext

I had a mild fever and chills, fatigue, muscle aches, sinus pressure, runny nose, and runny eyes. I also had phlegm drainage in the chest and a cough. This was the worst I had felt in a long time. I took a home antigen test and got a positive result. We called the doctor, and I was prescribed Paxlovid. I took the Paxlovid for five days. It wasn't about the seventh day that I noticed an improvement, though I still had some COVID-19 symptoms. On the eighth day, I felt markedly better and was able to get up and move around.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 22FEB2023 - Home Antigen Test - Positive Result;
Aktuelle Erkrankungen: None
Vorgeschichte: Coronary Artery Disease (Has Stent in Right Coronary Artery)
Andere Medikamente: Atorvastatin; Baby Aspirin; Claritin; Famotidine; Glucosamine Chondroitin; Fish Oil; CoQ10; Metamucil
Allergien: None
Vorherige Impfungen: -

VAERS 2590294

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 02.03.2023
Impfdatum: 11.10.2022
Beginn: 15.02.2023
Tage bis Beginn: 127,0
Dosis: 5
Route/Site: - / -

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

COVID-19 Dyspnoea SARS-CoV-2 test positive

Symptomtext

02/15/23 presents to ED for "SOB". PMHx of " arthritis, basal cell carcinoma, hypertension, stroke, history of cardiac catheterization, PFO"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 02/15/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2589736

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 01.03.2023
Impfdatum: 01.11.2022
Beginn: 02.11.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Asthenia Mobility decreased Pain in extremity X-ray normal

Symptomtext

My arm starting hurting the next day and it has not stopped since. I can feel the exact spott the shot ws give when I move my arm. It has now been 4 months and I never had a reaction to any of the other injections. I went Urgent Care on 01/09/2023 My right arm was X-Rayed it did not show anything. The PA gave me some arm strengthening exercises to do, however that has not helped. This is not normal I feel like I have lost strength and mobility in it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: 01/09/2023 x-ray
Aktuelle Erkrankungen: NONE
Vorgeschichte: hbp, obesity
Andere Medikamente: LISINOPRIL/HCTZ 20/12.5MG TAB, ANASTROZOLE 1 MG TAB
Allergien: NONE
Vorherige Impfungen: -

VAERS 2584326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: NJ
Alter: 58,0
Geschlecht: F
Eingang: 20.02.2023
Impfdatum: 18.11.2022
Beginn: 25.11.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: IM / LA

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

Chest X-ray abnormal Cough Dyspnoea Heart rate increased Heart rate irregular Pneumonitis

Symptomtext

I experienced shortness of breath, I could not carry anything without losing my breath, my heart rate was very rapid and was jumping very high and coughing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: X-ray results showed inflamed lung
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: Pfizer 01/23/2021, I experienced inflammation in my hands

VAERS 2582899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

moderat

Staat: TX
Alter: 70,0
Geschlecht: F
Eingang: 20.02.2023
Impfdatum: 23.11.2022
Beginn: 24.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: OT / LA

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

Injected limb mobility decreased Injection site nerve damage Vaccination site nerve damage

Symptomtext

nerve damage on her left deltoid where the injection site was; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). A 70-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 23Nov2022 at 11:45 as dose 4 (booster), single (Lot number: GJ3275) at the age of 70 years intramuscular, in left deltoid for covid-19 immunisation. The patient's relevant medical history included: "Hyperlipidemia" (unspecified if ongoing); "pain" (unspecified if ongoing); "bone disease" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Covid-19 vaccine (Dose: 1; unknown manufacturer), for COVID-19 immunization; Covid-19 vaccine (Dose: 2; unknown manufacturer), for COVID-19 immunization; Covid-19 vaccine (Dose: 3; unknown manufacturer), for COVID-19 immunization. The following information was reported: VACCINATION SITE NERVE DAMAGE (non-serious) with onset 24Nov2022, outcome "not recovered", described as "nerve damage on her left deltoid where the injection site was". The event "nerve damage on her left deltoid where the injection site was" required physician office visit. It was unknown if therapeutic measures were taken as a result of vaccination site nerve damage. Additional information: The patient had no other vaccine in four weeks. The patient had no known allergy. She's stating been going to several doctors for treatment of her nerve damage. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bone disorder; Hyperlipidemia; Pain
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2582899

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: TX
Alter: 70,0
Geschlecht: F
Eingang: 20.02.2023
Impfdatum: 23.11.2022
Beginn: 24.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Injected limb mobility decreased Injection site nerve damage Vaccination site nerve damage

Symptomtext

nerve damage on her left deltoid where the injection site was; This is a spontaneous report received from a contactable reporter(s) (Pharmacist). A 70-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 23Nov2022 at 11:45 as dose 4 (booster), single (Lot number: GJ3275) at the age of 70 years intramuscular, in left deltoid for covid-19 immunisation. The patient's relevant medical history included: "Hyperlipidemia" (unspecified if ongoing); "pain" (unspecified if ongoing); "bone disease" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: Covid-19 vaccine (Dose: 1; unknown manufacturer), for COVID-19 immunization; Covid-19 vaccine (Dose: 2; unknown manufacturer), for COVID-19 immunization; Covid-19 vaccine (Dose: 3; unknown manufacturer), for COVID-19 immunization. The following information was reported: VACCINATION SITE NERVE DAMAGE (non-serious) with onset 24Nov2022, outcome "not recovered", described as "nerve damage on her left deltoid where the injection site was". The event "nerve damage on her left deltoid where the injection site was" required physician office visit. It was unknown if therapeutic measures were taken as a result of vaccination site nerve damage. Additional information: The patient had no other vaccine in four weeks. The patient had no known allergy. She's stating been going to several doctors for treatment of her nerve damage. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Bone disorder; Hyperlipidemia; Pain
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2582389

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: NJ
Alter: 65,0
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 18.12.2022
Beginn: 18.12.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Heart rate increased Hyperhidrosis Palpitations

Symptomtext

1. Feelings of having a fast-beating and pounding heart in the night. 2. Sweet often during the day without excise.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Pre-diabetes
Andere Medikamente: No
Allergien: N/A
Vorherige Impfungen: fatigue and tired for several months. 64 years. Vaccine date: 5/1/2021, Janssen vaccine.

VAERS 2581647

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: ID
Alter: 90,0
Geschlecht: F
Eingang: 14.02.2023
Impfdatum: 05.01.2023
Beginn: 24.01.2023
Tage bis Beginn: 19,0
Dosis: 4
Route/Site: IM / LA

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

Computerised tomogram Condition aggravated Dementia Fall Hip arthroplasty Hip fracture Laboratory test Memory impairment X-ray

Symptomtext

Admit 1/24/23 with right hip fracture after a mechanical fall, s/p right hemiarthroplasty 1/25. Now discharged and readmitted twice with agitated dementia. Currently admitted. He previously lived at home with his spouse and will no longer be able to return home. He needs permanent memory care placement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: CT, xray, labs
Aktuelle Erkrankungen: None
Vorgeschichte: Very hard of hearing with hearing aids, dementia, A-fib on Xarelto, CKD stage IIIa, CAD, HTN, HLD, hypothyroidism, chronic pain on Norco 10/325 mg 2 tablets 4 times daily at baseline.
Andere Medikamente: diclofenac sodium (VOLTAREN) 1 % Gel Apply 4 g topically 4 (four) times daily. ? donepeziL (ARICEPT) 5 MG tablet TAKE 1 TABLET(5 MG) BY MOUTH EVERY NIGHT ? DULoxetine (CYMBALTA) 30 MG capsule TAKE 1 CAPSULE BY MOUTH EVERY DAY AND TAKE WIT
Allergien: NKA
Vorherige Impfungen: -

VAERS 2580355

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: PA
Alter: 33,0
Geschlecht: M
Eingang: 13.02.2023
Impfdatum: 11.11.2022
Beginn: 26.01.2023
Tage bis Beginn: 76,0
Dosis: 4
Route/Site: IM / LA

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

Anxiety Blood test normal Chest X-ray normal Computerised tomogram normal Condition aggravated Dyspnoea Functional residual capacity decreased Hypoaesthesia Laboratory test Pulmonary function test abnormal Respiratory symptom Scan with contrast normal

Symptomtext

I was having an issue with numbness in my right ear. I went to the hospital on January 26, 2023, for it, and they did a whole battery of test, and they could not find anything. In addition, I have been dealing with some shortness of breath in the last month or 2. I had a Pulmonary Function Test, and the results show FRC decreased, and SBC reduced. No medication has been prescribed yet, but an inhaler has been suggested. We have also looked into anxiety as I am now being treated for it, but those symptoms started after my 2nd dose of the vaccine. My symptoms have improved since starting the medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: CT Scan w/wo Contrast January 26, 2023 normal. Chest X-ray January 26, 2023 normal. Blood Panel January 26, 2023 normal. Pulmonary Function Test January 27, 2023 FRC decreased and SBC reduced. Several mild symptoms observed.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Pre-Hypertension; Elevated White Blood Count; Obesity; Depression/Anxiety; Motion Sickness since 2013
Andere Medikamente: Lisinopril; omeprazole; bupropion; multivitamin; COLACE; semaglutide
Allergien: Gluten; MUCINEX
Vorherige Impfungen: COVID 19 Dose Pfizer developed body aches

VAERS 2574281

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 02.02.2023
Impfdatum: 01.11.2022
Beginn: 01.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / UN

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

Abdominal distension Abdominal pain Abdominal pain lower Gait disturbance Menstrual disorder Mobility decreased Pain in extremity Posture abnormal

Symptomtext

I had my vaccination on 11/01/2022. I had abdominal pain in 11/2022 which was very painful and could not walk. I was not able to get out of bed and I was bent at the waist. Lower abdominal pain to the right extremities to include bloating and distended abdominal. This happened in 11/2022 12/2022 and 01/2023 during my menstrual cycle. I had a doctor appointment on 01/31/2023 and was ordered an ultrasound. This appointment is in the near future.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Ultrasound 2023 scheduled
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Vitamin C; vitamin D; iron
Allergien: N/A
Vorherige Impfungen: -

VAERS 2567729

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: WI
Alter: 70,0
Geschlecht: F
Eingang: 25.01.2023
Impfdatum: 06.12.2022
Beginn: 06.12.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Palpitations

Symptomtext

Heart palpitations

Weitere VAERSDATA-Felder

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

VAERS 2566931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: TX
Alter: 59,0
Geschlecht: F
Eingang: 24.01.2023
Impfdatum: 18.10.2022
Beginn: 25.12.2022
Tage bis Beginn: 68,0
Dosis: 5
Route/Site: SYR / LA

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

Blood test normal COVID-19 Computerised tomogram thorax abnormal Dyspnoea Fatigue Full blood count abnormal Headache Influenza virus test positive Malaise Mononucleosis heterophile test positive Pain Pneumonia Pyrexia Respiratory syncytial virus test negative SARS-CoV-2 test positive Streptococcus test negative

Symptomtext

My COVID-19 infection symptoms started on 12/25/2022 in the morning. I felt like I had a head cold. On 12/28/2022 my symptoms worsened. I had body aches, extreme fatigued, shortness of breath, headaches and low grade fever. I went to the ER at 6:15PM since I was experiencing difficulty breathing. They did COVID-19, Flu, Strep, and RSV tests which were negative. They thought I had Bronchitis. I don't remember if they prescribed anything to take. On 12/31/2022 in the afternoon my symptoms were getting worse so I went back to the ER again. I was positive for SARS (COVID-19), Flu and Mono. They also did CT scan where it showed that both of my lungs had infections. They did all kinds of things. They gave me IV fluids. They told me that it was moderate it wasn't to the severe side. On 01/01/2023 they released with medications, breathing treatments, and oxygen. I have high blood count. I went back with the same symptoms in the ER on 01/02/2023. I went back again on 01/03/2023 they kept me for the night with medications that was the last time for ER visit I started feeling better from 01/07/2023. I went to my regular doctor for a follow-up on 01/17/2023 everything showed normal in my blood work. As of today I am feeling better except my oxygen level is lower than normal. It's not back where it should be but all the other symptoms are gone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 31DEC2022 COVID-19 test positive; 31DEC2022 Flu test positive; 31DEC2022 Mono test positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2566769

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: WI
Alter: 46,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 21.10.2022
Beginn: 30.12.2022
Tage bis Beginn: 70,0
Dosis: 4
Route/Site: IM / LA

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

Atrial fibrillation Blood urine present Bronchitis Computerised tomogram abdomen abnormal Condition aggravated Electrocardiogram ambulatory abnormal Flank pain Nephrolithiasis Palpitations Pneumonia Supraventricular tachycardia Thyroid function test normal Urine analysis abnormal

Symptomtext

I ended up having to go to urgent care twice for pneumonia and bronchitis and they prescribed albuterol, prednisone, and TESSALON PERLES. They also prescribed azithromycin. Pneumonia and Bronchitis which developed in November of 2022 and lasted through the beginning of January 2023. I had right flank pain and blood in the urine. I went to the emergency room and ended up passing the kidney stone. I was given pain medication and FLOMAX. I also developed atrial fibrillation at the beginning of January. I had a couple of minutes of a fib. I noticed my heart having palpitations and I captured it on my smart watch. I was placed on a Holter monitor for 5 days starting January 10, 2023. The report indicated that I was having PAC and PVC's as well as SVT's over the course of 5 days. They tested my thyroid and it was normal. I have a cardiology appointment next week. I also have to follow up with nephrology. I was placed on potassium citrate for the kidney stones. I am currently ok and there have not been any more problems since but we are still checking to see if there's any more concern. I would say that I have recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Holter monitor January 10, 2023, report indicated that I was having PAC and PVC's as well as SVT's over the course of 5 days. Cat scan December 28, 2022, identified the stone and a few more small stones bilateral. Urinalysis December 28, 2022 Blood in Urine January 19, 2023, normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension; Exertional Asthma; Fatty Liver; Kidney Stones
Andere Medikamente: PROTONIX; vitamin D; fish oil; amlodipine; albuterol inhaler
Allergien: Penicillin; COMPAZINE; REGULON
Vorherige Impfungen: Pfizer dose 3 and 4, I experienced fever chills and being tired that lasted for 1 to 2 days.

VAERS 2564638

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: NY
Alter: 55,0
Geschlecht: F
Eingang: 20.01.2023
Impfdatum: 01.11.2022
Beginn: 01.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Angiocardiogram Angiogram pulmonary COVID-19 Cardiac imaging procedure Computerised tomogram thorax Dyspnoea Dyspnoea exertional Echocardiogram Electrocardiogram abnormal Fibrin D dimer increased Influenza virus test Laboratory test Malaise Mobility decreased Palpitations Ultrasound liver

Symptomtext

I had my 4th vaccine on November 8th, 2023. Initially after the bivalent vaccine, I had Covid-19 symptoms, which I assumed was normal. These lasted a long time and progressed to worse symptoms. Within three weeks, I had significant shortness of breath (even to speak), exertion intolerance, and racing heart without exertion. I stood up from a chair and my heart raced over 130. I saw a Cardiologist on Nov. 28. He did tests to rule out heart muscle damage- labs for Cardiac Inflammation and D- Dimer. By the next day, I learned my D Dimer was between 900-950. I was still very symptomatic and had to go to the Emergency Room to rule out PE- THE SAME THING THAT HAPPENED AFTER MY 3RD VACCINE, BUT WORSE. I was in the hospital for 3 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 4,0
Labordaten: Local Hospital: Nov. 29- Dec. 2, 2023 Labs EKG Chest CT and CTA to rule out PE Transthoracic Echocardiogram Cardiac MRI CTA of Coronary Arteries Ultrasound of Liver Covid-19 testing and Respiratory Illness Profile testing (Flu, etc.)
Aktuelle Erkrankungen: Long Covid- PASC Diagnosed in March of 2021 @ local Clinic Had Alpha Variant of Covid in Nov. 2020 before any treatments were available- had no treatment Extreme Fatigue, Post Exertional Malaise, Brain Fog symptoms, Abnormal Liver Enzymes
Vorgeschichte: Congenital Heart Disease High Blood Pressure Borderline A1C Severe Apnea (OSA)- controlled Partial collapse in Right Lung
Andere Medikamente: Lisinopril, Levothyroxine, Metformin, Toprol, Prozac, Low Dose Naltrexone, Atorvastatin, Baby Aspirin, Lasix, Alprazolam
Allergien: Allergies to environmental substances- grass, trees, ragweed, etc. Sensitivity to Lidocaine- high doses of novocaine
Vorherige Impfungen: I had a similar reaction to my 3rd Covid-19 vaccine by Pfizer. This was reported to VAERS- I had shortness of breath, tachycardi

VAERS 2563337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 19.01.2023
Impfdatum: 14.10.2022
Beginn: 21.12.2022
Tage bis Beginn: 68,0
Dosis: 5
Route/Site: IM / RA

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

Asthma COVID-19 Condition aggravated Diarrhoea Dysgeusia Fatigue Feeling abnormal Gastrooesophageal reflux disease Malaise Oropharyngeal pain Pain in extremity Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I had the normal sore arm after receiving the vaccine and I was tired for day. I started feeling sick on 12/21/2022 with a really sore throat down low. I throat it was reflux and treated it like it was reflux. As the day progressed, my symptoms got worse. My nose was running, and I went through tissues like crazy. I felt really bad, and I felt out of it. I tested positive with a home test on 12/22/2022. I contacted my doctor, and I was given the prescription PAXLOVID. I had a metallic taste in my mouth, and I had diarrhea on Christmas day and the day after. I did have a rebound of COVID-19 and was sick again for six whole days. As of today, I feel that my asthma is worse since having COVID-19. I have to use my inhaler more than I did prior to COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 22DEC2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma; Migraines
Andere Medikamente: Spironolactone; montelukast; vitamin D3; vitamin B12; iron; magnesium; pumpkin seed oil; estradiol
Allergien: Egg; shellfish; basil
Vorherige Impfungen: -

VAERS 2560082

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 14.01.2023
Impfdatum: 24.10.2022
Beginn: 13.01.2023
Tage bis Beginn: 81,0
Dosis: 5
Route/Site: IM / -

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

Aphasia COVID-19 Chest pain Dizziness SARS-CoV-2 test positive

Symptomtext

73 y.o. male with a PMH of prostate CA, depression, anxiety, renal artery stenosis, orthostatic hypotension, and recent admission 1/11-1/12/23 for CP, dizziness, found to be covid positive. He presented 1/13/2023 with sudden aphasia. Per wife, last known well 1130. S/p TNK @ 1309.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2553062

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: OH
Alter: 18,0
Geschlecht: M
Eingang: 07.01.2023
Impfdatum: 04.01.2023
Beginn: 04.01.2023
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / -

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

Bronchitis Condition aggravated Cough Dyspnoea

Symptomtext

had resolving bronchitis but cough and sob worse few hours after vaccination with bivalent vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: had xr before, 2 visits for uri/ bronchitis
Aktuelle Erkrankungen: bronchitis just prior, made worse from vaccine
Vorgeschichte: none
Andere Medikamente: tessalon, albuterol
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2550326

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 09.12.2022
Beginn: 11.12.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / LA

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

Dyspnoea Fatigue Full blood count abnormal Platelet count decreased

Symptomtext

About 48 after dose 4 I began to feel fatigued, and I had shortness of breath. I let my doctor know about my symptoms. I had lab work done and my blood work showed that my platelet levels had dropped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Blood panel, CBC, abnormal, 12/12/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Idiopathic thrombocytopenic purpura; ITP
Andere Medikamente: Hydrochlorothiazide; TAVALISSE; EUCERIN
Allergien: PROMACTA
Vorherige Impfungen: -

VAERS 2546965

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge gj3275

moderat

Staat: TN
Alter: 60,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 10.11.2022
Beginn: 21.11.2022
Tage bis Beginn: 11,0
Dosis: 4
Route/Site: IM / AR

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

Condition aggravated Skin ulcer Vasculitic ulcer

Symptomtext

Worsening vasculitic ulcers to bilateral lower extremities. Multiple scattered new ulcers as well as worsening of established ulcer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: Vasculitis (biopsy confirmed), Diabetes, Hypertension
Andere Medikamente: Metformin 500 mg daily, amlodipine 10 mg, ferric X 150 mg, Celebrex 200 mg, triamterene hydrochlorothiazide 37.5 mg/25 mg, sertraline 50 mg, vitamin D3 25 mcg (1000 units).
Allergien: NKA
Vorherige Impfungen: -

VAERS 2544534

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: NJ
Alter: 75,0
Geschlecht: M
Eingang: 28.12.2022
Impfdatum: 12.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 10,0
Dosis: 5
Route/Site: SYR / LA

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

Arthropathy Body temperature increased COVID-19 Eye pain Feeling abnormal Feeling cold Headache Nasal disorder Oropharyngeal pain Pain Rhinorrhoea SARS-CoV-2 test positive Skin disorder Tremor

Symptomtext

When I first noticed the symptoms, it was a running nose and I thought it was dust or allergies. Then I started to not feel like myself. I started to get a sore throat and I thought right away I should test myself and I took a test after supper. I tested myself and noticed, I was positive. I went to bed and when I got up my wife called urgent care. They did a PCR test. Then we went home, by the time I got home I started to feel worse, my joints, arms, skin and a really bad headache started, I also started shaking and I felt very cold. My temp at home was 100.5. That day I just kind of sat around, I calmed down from the shakes after a while. I slept mostly and the headache was bad, and my eyes were hurting. My nose and throat did get better. Going to bed was rough because I was so cold and still a little shaky. As days went on it did get better and better. And today I feel a bit more normal. I still have a little headache and body aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: PCR- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Arthritis
Andere Medikamente: Vitamin A, Vitamin B, Vitamin C, Vitamin D
Allergien: Latex, Crab
Vorherige Impfungen: Flu vaccine, would get the flu right after

VAERS 2544531

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj3275

moderat

Staat: PA
Alter: 27,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 27.12.2022
Beginn: 27.12.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Fatigue Heart rate increased Myalgia Tachycardia

Symptomtext

Approximately 6 hours after the injection I began to experience tachycardia at rest. My resting heart rate increased to 115-120bpm. I had typical post vaccine symptoms such as muscle aches and fatigue but the tachycardia is the reason for this report. Tachycardia self-resolved at approximately 23 hours post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: -
Labordaten: None. No laboratory testing was conducted and I did not seek medical attention. This is the second time this has happened to me after a Pfizer COVID-19 vaccination and no laboratory testing was done when I sought medical care during the first occurrence.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multivitamin
Allergien: Gluten Allergy
Vorherige Impfungen: Pfizer COVID-19 (dose 2) on 10/20/2022. I experienced tachycardia within 8 hours post vaccination and continued until it self re

VAERS 2543834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: WA
Alter: 47,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 30.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / RA

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

Chills Condition aggravated Dyskinesia Heart rate increased Multiple sclerosis relapse Muscle spasms Pain Speech disorder

Symptomtext

8PM - body aches and chills 10:15pm to 11:30pm - uncontrollable body spasms/jerks. Heart rate increase and unable to talk normally. One word per spasm. Ended up having MS flare up from this reaction and still recovering from that.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No treatment. Did not go in. I probably should have gone in but felt like they couldn't do anything for me.
Aktuelle Erkrankungen: None
Vorgeschichte: Multiple Sclerosis
Andere Medikamente: None
Allergien: Gilenya
Vorherige Impfungen: -

VAERS 2543139

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: TN
Alter: 43,0
Geschlecht: F
Eingang: 26.12.2022
Impfdatum: 24.10.2022
Beginn: 19.11.2022
Tage bis Beginn: 26,0
Dosis: 4
Route/Site: IM / RA

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

Blood test normal Cognitive disorder Dizziness Dyspnoea Electrocardiogram normal Fatigue Feeling abnormal Gait disturbance Hypoaesthesia Impaired work ability Magnetic resonance imaging head normal Magnetic resonance imaging spinal normal Muscular weakness Neurological examination normal Paraesthesia Scan with contrast normal Vision blurred Visual impairment

Symptomtext

11/19/22- woke up with severe dizziness and fatigue- improved slightly over the course of a week, but with progressive weakness (limb) and brain fog/cognitive impairment/vision problems. Started Methylprenisolone steroid pack on 11/25 and noted some improvement. Dizziness continued to rapidly improve but weakness persisted/worsened. Felt max improvement on day of 12/1, then took a serious turn. By late evening of 12/1, developed numbness/tingling in both arms. On 12/2 attempted a short walk and immediately both arms started to tingle and went numb and shortly after the soles of both feet began to tingle. Attempted to drive later shortly after dark and was unable to focus eyes- called for assistance. Became progressively weaker and woke on 12/5 pm with difficulty breathing. Also unable to walk more than a few steps- needed assistance, Went to ER on 12/6, EKG normal, MRI of brain and spine with and without contrast was normal, sent home in am of 12/7. Saw PCP on 12/7 and started Prednisone 60 mg daily (1mg/kg). Noted improvement second day and was able to walk with pole. Continued to walk with pole for the next week. Dizziness some better, but still not able to drive, eyes still out of focus. Have tapered down on steroids, currently on 20 mg on 12/26/22. Able to drive and walk without assistance, but still with some brain fog and severe fatigue. Have not been able to work in 6 weeks. Saw Neuro on 12/20 who stated exam was fine and problems were not neuro related. Did not perform any evaluation of cognitive function- results were based on touching nose with finger and normal reflexes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: All tests have returned negative- MRI and various blood tests
Aktuelle Erkrankungen: possible viral illness 10/10, upper respiratory, resolved in 1-2 days
Vorgeschichte: Grave's disease, post-radioactive iodide ablation, on synthroid Chronic GERD- on omeprazole Tachycardia and migraines- managed with atenolol History of hypercholesterolemia- managed with rosuvastatin 5 mg M/W/F Probiotics for gut health and melatonin for sleep maintenance
Andere Medikamente: Synthroid, Omeprazole, Rosuvastatin, Atenolol, Zyrtec, Melatonin, Probiotics
Allergien: NKA
Vorherige Impfungen: -

VAERS 2542806

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

moderat

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 24.12.2022
Impfdatum: 14.12.2022
Beginn: 14.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Balance disorder Disorientation Hypertension Immediate post-injection reaction Nausea Vomiting

Symptomtext

Immediately after injection patient was getting out of chair and lost balance; they were caught and sat down to recover. Patient was instructed to either lay down with feet up or sit with head between knees, due to age, patient sat with head between knees. They shortly developed nausea and vomiting. After 15-20 minutes patient continued with symptoms and EMS was called. They evaluated patient and took them to hospital for further evaluation and care. According to patient's son, patient was kept at hospital for a few days for care and recovery. Patient had disorientation and uncontrollable hypertension the following days and nothing further was reported from family. Patient is now at home recovering, still a little disorientated but moving around and back to normal duties.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: 4,0
Labordaten: None reported
Aktuelle Erkrankungen: None Reported
Vorgeschichte: None reported
Andere Medikamente: unknown
Allergien: No known drug allergies
Vorherige Impfungen: -

VAERS 2538481

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 20.12.2022
Impfdatum: 07.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Breast pain Chest pain

Symptomtext

Pain deep in left chest/breast.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: None
Vorgeschichte: 5 years post double mastectomy, breast cancer
Andere Medikamente: Arimidex, multivitamin, turmeric, biotin, glucosamine
Allergien: Penicillin and fentanyl
Vorherige Impfungen: -

VAERS 2531308

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: IL
Alter: 49,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 13.12.2022
Beginn: 14.12.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Feeling abnormal Hypoaesthesia Paraesthesia

Symptomtext

Patient complains of left sided face numbness and tingling. She stated that it started very early this morning, 12/14/22 and complains that it is getting worse. She states that her face feels swollen and droopy although it visibly is not. She has no complaints of shortness of breath or loss of function in any form. She still has control of her facial muscles. The covid nurse hotline and the nurse at her PCP advised her to call the pharmacy. After consulting with other pharmacists, it was recommended to the patient to continue monitoring her symptoms as well as trying ibuprofen and Benadryl/other antihistamine in case it is a delayed inflammatory response. She is going to follow up with another phone call to her PCP 12/15/222 if her symptoms do not improve.

Weitere VAERSDATA-Felder

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

VAERS 2530173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: TN
Alter: 74,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 13.12.2022
Beginn: 13.12.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Dizziness Hypertension Paraesthesia

Symptomtext

PATIENT WAS GIVEN A PFIZER BIVALENT COVID BOOSTER AT APPROXIMATELY 2:50PM TODAY. SHE WAITED IN HER CAR FOR APPROXIMATELY 10 MINUTES THEN RE-ENTERED THE HEALTH DEPARTMENT WITH COMPLAINT OF FEELING "TINGLY". PT DENIED FEELING OF THROAT SWELLING OR SHORTNESS OF BREATH, DENIES CHEST PAIN. STATES SHE FEELS "WOOZY". B/P CHECKED AND WAS 226/94 WITH AUTOMATED CUFF, 220/104 MANUALLY, BOTH IN RIGHT ARM. PULSE 73, O2 SAT 98% ON ROOM AIR, TEMP 97.1. CHEEKS ARE RED BUT PT STATES THEY ARE "ALWAYS THAT WAY". SON ARRIVED AT HEALTH DEPT. PT HAD CALLED HIM WHILE SHE WAS IN HER VEHICLE. EMS DISPATCHED TO HEALTH DEPARTMENT, APN EVALUATED PATIENT AND PHONED MEDICAL DIRECTOR. APN/MD ADVISED TO HOLD EPINEPHRINE AT THIS TIME. EMS EVALUATED PATIENT. SON AND PATIENT DECIDED HE WOULD TAKE HER BY PRIVATE VEHICLE TO ER FOR EVAL OF HER BLOOD PRESSURE. PT REPORTS SHE HAD NOT SEEN PCP SINCE SEPT 2022 AND HER B/P WAS "OK" THEN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE REPORTED
Vorgeschichte: HYPERTENSION
Andere Medikamente: AMLODIPINE 2.5MG, PT STATES SHE ALSO TAKES A CHOLESTEROL MEDICATION BUT CANNOT RECALL THE NAME
Allergien: NONE LISTED
Vorherige Impfungen: -

VAERS 2528491

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: CO
Alter: 43,0
Geschlecht: F
Eingang: 11.12.2022
Impfdatum: 02.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: SYR / LA

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

Anosmia Atrophy Contusion Cystitis Fatigue Feeling abnormal Fungal infection Hypoaesthesia Illness Intermenstrual bleeding Limb discomfort Mobility decreased Muscular weakness Nervous system disorder Sinusitis Tendon injury Tension headache

Symptomtext

Got really sick, and tired and was in bed for 3 days....escalated to Sinus infection, I lost my sense of smell which was really weird becasue I have had sinus infections my whole life and never had any entire loss of smell, I tested for covid before and after 4 days in a row and no covid....my smell finally came back but was experiencing nerve issues in right foot.... my right foot feeling heavy and numbness, also I have been having muscle weakness in legs and looks like they have atrophied a little (not sure if this is because I stopped running due to injury in hamstring)...... also bruising a lot and have had bleeding in between periods. After the sinus infection I also got a bladder infection followed by a yeast infection. It was like the vaccine completely wiped me out my head and body have felt weird since. Now to date I still have a little numbness in my right foot, my smell is back, I have had a few tension headaches that wrap around my entire head (treated with massage and chiropractor) which I have never had before. My first covid shot I also got really sick and my 4th one I had issues too with lymph nodes in armpit swelling and tons of muscle pains and aches. Have not gone to all my doctors yet, I am going to schedule one with main physician soon.... this week going to OBGYN for ultrasounds and blood work first from the weird bleeding and infections following vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none but very busy and run down
Vorgeschichte: asthma, sinus infections, bladder infections
Andere Medikamente: propanol 20 mg Adderall 5 mg Potassim 20 mg daily vitamins D and B12 advil on occasion
Allergien: sulfa drugs
Vorherige Impfungen: all the covid related shots

VAERS 2528460

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: WA
Alter: 14,0
Geschlecht: M
Eingang: 10.12.2022
Impfdatum: 03.12.2022
Beginn: 10.12.2022
Tage bis Beginn: 7,0
Dosis: 4
Route/Site: IM / LA

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

Chest pain

Symptomtext

Chest pains started the night of vaccine and lasted for 2 days and on 12/05/2022 the symptoms were resolved. Mom mentioned there was no need for Doctor visit as they were aware of the potential side effect of this vaccine and the symptoms were mild.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 2528321

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: FL
Alter: 19,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 28.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: IM / LA

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

Antinuclear antibody Asthenia Blood triglycerides decreased Chest discomfort Chest pain Dyspnoea exertional Exercise tolerance decreased Fatigue Fibrin D dimer increased Haemoglobin normal Impaired work ability Laboratory test normal Loss of personal independence in daily activities Metabolic function test normal Tachycardia White blood cell count normal

Symptomtext

Weakness, disproportionate fatigue, chest pain and tightness with exertion, shortness of breath with exertion. Unable to continue working retail job, dance for college dance classes, and photography due to symptom onset and worsening. Unable to participate in desired social activities due to weakness and fatigue. Can only walk short distances and not stand for long, because of symptoms. Tachycardia with minimal exertion such as walking and activities of daily living. Difficulty washing hair, folding clothes due to weakness and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: D-Dimer, Quantitative - 0.87 mcg/mL FEU (November 9, 2022) Ana Titer - 1:160 titer (November 9, 2022) White Blood Count: normal (November 22, 2022) Comprehensive Metabolic Panel: normal (November 22, 2022) Hemoglobin pre diabetic: normal (November 22, 2022) Triglycerides: low (November 22, 2022) De Dimer: negative (November 22, 2022)
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: sertraline 50 mg tablet (ZOLOFT) 1 (one) time each day. cetirizine 10 mg tablet (ZyrTEC) 10 mg by mouth 1 (one) time each day.
Allergien: Amoxicillin: Rash
Vorherige Impfungen: -

VAERS 2527924

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: FL
Alter: 59,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 10.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Cyst Cyst drainage Influenza like illness Migraine Pain Ultrasound scan X-ray abnormal

Symptomtext

I had really bad flu like symptoms which I took TYLENOL for. I developed a cyst on the top of my foot about a week after the vaccine. It painful as it continued to grow. The podiatrist saw me on December 5th, 2022. She was able to drain the cyst a little. She advised to take TYLENOL for the pain and keep it wrapped. The symptoms have improved but I have not completely. I have migraines and plan to see a doctor regarding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: X-ray December 5th, 2022, lump seen, Ultrasound December 5th, 2022 cyst located.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Lupus results inconclusive
Andere Medikamente: Indomethacin; VALTREX; TYLENOL; TUMS
Allergien: N/A
Vorherige Impfungen: -

VAERS 2527778

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: TX
Alter: 55,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 02.12.2022
Beginn: 06.12.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: SYR / RA

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

Chest pain Cough Feeling abnormal Glassy eyes Head discomfort Human metapneumovirus test positive Influenza virus test negative Malaise Musculoskeletal stiffness Nasal congestion Pain Paranasal sinus discomfort Respiratory viral panel SARS-CoV-2 test negative Throat irritation

Symptomtext

The cough started Tuesday night all night long. It made my throat really scratchy and my chest was painful. I also slept with VICKS vapor rub on my chest and throat. The next day when I got up, my eyes were so glassy. I took my allergy medication and the symptoms alleviated a little bit, but the cough persisted. I felt a little achy and stiff, but I thought I was fine. I have some nasal congestion and pressure on my forehead, like sinus pressure. I do not have a fever or sore throat, but I do some have energy. Every day I feel a little bit worse. When the doctor called, she told me to get DAYQUIL and NYQUIL. I took NYQUIL and I was able to sleep much better because it suppressed the cough. When I went to the doctor Wednesday, they tested for flu and COVID-19 and those came back negative. We also did a panel for other respiratory viruses, and she said I came back positive for metapneumovirus. I am fully symptomatic today, but I started full symptoms on Wednesday. Today is my third day staying home sick. I wasn't sure if this vaccine had weakened my immune system or I'm not sure what happened. I'm just concerned. I've also been taking some ADVIL daily to help with symptoms. Treating it with over the counter medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 12/06/2022 COVID-19 at home test negative; 12/07/2022 flu test negative; 12/07/2022 COVID-19 test negative; 12/07/2022 Respiratory infection panel positive for Metapneumovirus
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: ZYRTEC; vitamin D3; vitamin B complex; zinc; baby aspirin; ALIGN probiotic; AIRBORNE vitamin C prevention; FLONASE
Allergien: Tetracycline
Vorherige Impfungen: -

VAERS 2525500

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: WI
Alter: 36,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 06.12.2022
Beginn: 06.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

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

Hypoaesthesia Neck pain Paraesthesia

Symptomtext

There is numbness and tingling in my left arm and hand. That did begin yesterday afternoon around 6PM, and that's continued today as well. There has been accompanied neck pain in the front of my neck that started around the same time and has continued. I did call the nurse from my doctor, and she noted to just monitor the symptoms and if they do not get any better to come in and be seen.

Weitere VAERSDATA-Felder

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

VAERS 2522735

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: WA
Alter: 42,0
Geschlecht: M
Eingang: 04.12.2022
Impfdatum: 02.12.2022
Beginn: 04.12.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Migraine Toothache

Symptomtext

Beginning at noon on Sunday 12/4 I started experiencing agonizing pain in the teeth on the left side of my mouth - both upper and lower. It has been alternating to different teeth and has persisted for the past 8.5 hours. Ibuprofen has done nothing to reduce the pain. The pain has been so great it?s induced a migraine headache several times.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Covid 19
Vorgeschichte: None
Andere Medikamente: Sertraline, bupropion
Allergien: None
Vorherige Impfungen: -

VAERS 2522404

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

moderat

Staat: VA
Alter: 70,0
Geschlecht: F
Eingang: 03.12.2022
Impfdatum: 28.11.2022
Beginn: 28.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / LA

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

Blood pressure abnormal Chest pain Interchange of vaccine products Malaise

Symptomtext

This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. A 70-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Nov2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 70 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure", start date: 2012 (ongoing), notes: high blood pressure diagnosed 10 years ago. Concomitant medication(s) included: LISINOPRIL taken for hypertension, blood pressure abnormal; All of her previous COVID 19 vaccines have been four shots Moderna and she got the Pfizer COVID19 booster because the pharmacy did not have the Moderna booster available and said it was ok to mix them; the last booster dose of Moderna was in May and she had no side effects at all to the Moderna vaccines she received; also had a flu shot on 07Nov2022, she does not know the name of it or the manufacturer or lot, expiry date or to provide but it was at the doctor's office. Her last booster dose was in May, and it was Moderna. She had no side effects to the Moderna vaccines. She had a flu shot 10Oct2022. Her patient card has no expiry date or for the Pfizer COVID booster dose. Had no treatment for the reported events. She had a dentist's appointment she was scared to took and she did not want to put any more chemicals in her body because she does not feel well and was cancelling her dentist's appointment due to not feeling well. No investigation and conditions were reported. These events do not require a visit to Emergency room. It was reported that the case was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: Blood pressure Abnormal; Result Unstructured Data: Test Result:Blood pressure Abnormal
Aktuelle Erkrankungen: Blood pressure high (high blood pressure diagnosed 10 years ago)
Vorgeschichte: -
Andere Medikamente: LISINOPRIL; TIMOLOL
Allergien: -
Vorherige Impfungen: -

VAERS 2522474

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ3275

moderat

Staat: MN
Alter: 42,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 01.11.2022
Beginn: 02.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

Arthritis Arthropathy Joint lock Mobility decreased Musculoskeletal stiffness Pain in extremity

Symptomtext

Since the vaccine however I am experiencing arthritis type symptoms on the right side of my body which is the side vaccine was administered. The next morning my whole side was stiff and my thumb locked. My big toe has pain my left leg at the top socket has pain and my big toe. I cannot move my thumb in the mornings. I felt like it was maybe trigger finger but other joints unrelated like my big toe are having trouble

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: I my OB Suggested going to a primary which I will but it?s ongoing and not getting better.?I am checking perm damage below because it?s been a month and I feel it?s probably permanent
Aktuelle Erkrankungen: Depression
Vorgeschichte: None
Andere Medikamente: Seroquel/ lamictal
Allergien: Cinnamon
Vorherige Impfungen: -

VAERS 2522235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 23.11.2022
Beginn: 23.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dyspnoea

Symptomtext

PATIENT EXPERIENCE SHORTNESS OF BREATH. 911 WAS CALLED PATIENT WAS TAKEN BY AMBULANCE. SPOKE TO PATIENT FOLLOWING WEEK AND STATED SHE WAS GIVEN OXYGEN AND BENADRYL.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: NONE KNOWN
Aktuelle Erkrankungen: COPD/ASTHMA
Vorgeschichte: ASTHMA COPD
Andere Medikamente: NONE LISTED USED RESCUE INHALER
Allergien: NONE REPORTED ON FORM
Vorherige Impfungen: -

VAERS 2520267

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 30.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Pain in extremity Paraesthesia

Symptomtext

Pt received Pfizer bivalent, after 10 minutes states that she is having tingling sensation in her right deltoids that irradiated to her hand. VS -68, 135/75, 98%. around 12:45 pm pt states that tingling sensation is improving, but she is experiencing pain in her right arm 4/10. 12:53 pm pt states that she was feeling better. ED precautions given, pt verbalized understanding. Pt was discharged home.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: IV contrast dye.
Vorherige Impfungen: -

VAERS 2511776

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

moderat

Staat: OH
Alter: 16,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 18.11.2022
Beginn: 18.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Feeling abnormal Hypotension Pallor

Symptomtext

patient felt off, not quite right. looked pale. BP which was low during her infliximab infusion continued to be in the 90/50s. Not tachcardic.. she had no neew findings on physical exam

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: none done. she was given 500 mL of normal saline and seemed to perk up with better color. her diastolic BP rose to 60s.
Aktuelle Erkrankungen: mononucleosis in October 2022
Vorgeschichte: Crohn's disease
Andere Medikamente: ? Indliximab levonorgestrel (MIRENA) 20 mcg/24 hours (8 yrs) 52 mg IUD^1 Each by INTRAUTERINE route as directed.^Disp: 1 Each^Rfl: 0 ? omeprazole (PRILOSEC) 20 mg capsule^Take 2 capsules by mouth once daily.^Disp: 180 capsule^Rfl: 3 ? ac
Allergien: ALLERGIES Allergen Reactions ? Omnicef [Cefdinir] Rash ? Toradol [Ketorolac] Rash, Itching ? Red Dye Rash
Vorherige Impfungen: -

VAERS 2510636

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: NC
Alter: 53,0
Geschlecht: M
Eingang: 17.11.2022
Impfdatum: 30.10.2022
Beginn: 30.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Arthralgia Bed rest Immediate post-injection reaction Injection site bruising Injection site haemorrhage Limb discomfort Mobility decreased Pain in extremity

Symptomtext

Bled at time of injection at point of needle insertion, sore upper arm/shoulder immediately following vaccination, discomfort/pain progressed for days in upper arm, movement of arm became limited for over two weeks, bed rest for six days treating with ibuprofen to treat pain and possible inflammation, bruising at injection site still visible 18 days post injection, mobility and discomfort improving.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Dr. conducted assessment on 11/16/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxine 50mcg, Atorvastatin 10mg,, multi-vitamin, B-complex, probiotic
Allergien: None
Vorherige Impfungen: -

VAERS 2503794

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: OH
Alter: 49,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 21.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 5,0
Dosis: 1
Route/Site: IM / LA

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

Eye pain Headache Migraine Myalgia Neck pain Neuralgia Tension headache X-ray normal

Symptomtext

I get a lot of migraines and tension headaches. So, between 10/21/2022 and 10/26/2022, I experienced some headaches that I didn't think much of. However, on 10/26/2022, I woke up with a headache that felt different than my typical headaches and that continued through the day. I tried treating it with ADVIL and TYLENOL which usually takes care of my headaches, but it did not work. It felt more like muscle or nerve pain and as it progressed it felt more like nerve pain coming from my neck and up over my head. This continued on until 11/03/2022, when it began to feel like it was coming from the base of my skull, over the top of my head, and into my eye socket. That nerve pass was causing me an intense amount of pain. I've experienced shingles on my head before and it felt very similar to that pain. However, I don't have a rash. I spoke with my mother, who was previously in the health care field about the possibility of internal shingles. I ultimately ended up going to the doctor and explained all of my pain issues but did not mention my recent vaccine, nor did they ask. It wasn't until I spoke with a friend about my experience, that I made a connection to my vaccine. I then did a bit of research and found that shingles has been reported in others post vaccine. My doctor is not treating me for shingles. They did prescribe TYLENOL with codeine, prednisone, gabapentin, and a muscle relaxer. The only thing they would have done differently, had I come within the first seven days would have been to prescribe an antiviral as well. I did message my doctor about the connection I made between my vaccine and the possibility of shingles, just to inform them of my discovery of the possible connection. I am supposed to contact my doctor again if the pain has not gone away in a few days. The pain is subsiding.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: 03NOV2022 X-ray of neck nothing unusual found
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines; Asthma
Andere Medikamente: WELLBUTRIN; TYLENOL; ADVIL; iron; vitamin D
Allergien: VICODIN
Vorherige Impfungen: -

VAERS 2502012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: TN
Alter: 51,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 25.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Blood urine present Breast swelling Condition aggravated Lymphadenopathy Mobility decreased Pelvic pain Ultrasound uterus abnormal Urine analysis Urine leukocyte esterase positive Uterine cyst Uterine enlargement Uterine leiomyoma

Symptomtext

Swollen lymph nodes under both arms, swollen breasts and severe pelvic pain started in the evening after the booster was given. Stayed in bed with heating pad for over 2 weeks now. Still experiencing severe pelvic pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Urinalysis completed with Trace amounts of Leukocytes and Trace amounts of Blood - 10/31/2022 Ultrasound of uterus revealed Enlarged uterus and several additional new fibroids and cysts - 11/7/2022.
Aktuelle Erkrankungen: None
Vorgeschichte: Uterine Fibroids
Andere Medikamente: Lisinopril, Clonidine
Allergien: None
Vorherige Impfungen: Swollen lymph nodes in left arm

VAERS 2500706

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: IA
Alter: 13,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 06.11.2022
Beginn: 06.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Fall Feeling hot Immediate post-injection reaction Thirst Tremor Unresponsive to stimuli

Symptomtext

Patient fell, became unresponsive, and was shaking withing 5 minutes of receiving the vaccinations. She woke up within 2 minutes but had difficulty breathing, felt hot, and needed water. EMS came to check her out and she ended up being okay after about 20-30 minutes.

Weitere VAERSDATA-Felder

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

VAERS 2499323

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj3275

moderat

Staat: WA
Alter: 30,0
Geschlecht: M
Eingang: 04.11.2022
Impfdatum: 21.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / AR

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

Condition aggravated Tic Tourette's disorder

Symptomtext

My motor tics got worse and more noticeable by clients of mine. I have minor Tourette?s. They are still worse and I?m hoping the side effects subside

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: I have minor Tourette?s since age 9. My motor tics have been worse and more noticeable by clients since the vaccine flu shot combo.
Vorgeschichte: -
Andere Medikamente: Lexapro 20mg Wellbutrin 150mg Both 1x daily
Allergien: Gluten intolerance. Intolerance to bananas almonds avocado salmon
Vorherige Impfungen: -

VAERS 2497227

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 02.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Dyspnoea Tongue disorder Tonsillar disorder

Symptomtext

Patient came in and requested to receive Pfizer bivalent booster. Upon order entry patient stated that when I get the vaccines I take my inhaler after but I forgot it today. Patient stated after receiving all three doses of the covid vaccine she felt a little short of breath but it went away after she used her inhaler. Allergist was notified of situation and suggested to watch her for 30 minutes after vaccination to observe for any reaction. 1703 patient was adminstered Pfizer Bivalent booster and at 1720 patient requested to use inhaler. Patient puffed 6 puffs and was monitored for 10 minutes without improvement. Upon visualization of the throat the throat was patent patient was AxOx4 speaking in full complete sentences. Patient skin was dry and warm to the touch. At 1745 patient was given IM Benadryl and Allergist was notified of situation. Patient stated she feels like she is getting better after IM Benadryl at 1755, Dr. requested ordered to monitor patient for another 30 minutes; if SOB worsens administer IM EPI and send to the ED, if patient states shes getting better she can be sent home. After 30 minutes of monitoring patient is AxOx4 speaking in full complete sentences with no SOB and in no acute distress. Patient was educated that if any S/S such as difficulty swallowing, uncontrollable coughing, worsening SOB to immediately go to the ER. Patient stated "I feel better my tongue and tonsils feel way better after the Benadryl I feel like I am good to go home." Patient ambulated with strong and steady gait out of vaccine clinic accompanied with husband and 2 kids at 1828.

Weitere VAERSDATA-Felder

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

VAERS 2496623

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

moderat

Staat: OH
Alter: 80,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 30.10.2022
Beginn: 30.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Anxiety Blood pressure increased Dizziness postural Immediate post-injection reaction Tachycardia

Symptomtext

Systemic: Hypotension-Mild, Systemic: Tachycardia-Mild, Additional Details: pt had dizziness upon standing immediately after receiving vaccine. pt may have stood up to fast causing dizziness and then had some anxiety with the dizziness. Blood pressure was slightly elevated

Weitere VAERSDATA-Felder

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

VAERS 2495112

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: GA
Alter: 62,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 17.10.2022
Beginn: 17.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

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

Blood test normal Dizziness Exercise tolerance decreased Fatigue Palpitations Urine analysis normal

Symptomtext

After the first few days, I was tired as I knew I would be. Then I started getting dizzy and having heart palpitations. I normally work out a lot and I couldn't even walk around the block. I got very dizzy and felt like I was going to pass out. That's what it has been so far. I get heart palpitations and I get exhausted every time I exert energy. It doesn't seem to be getting any better. It just seems to be getting worse. I did call the doctor on Wednesday and they say saw me on Thursday. They ran a lot of lab work and everything seems to be normal so far. I will be following up with them.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: 30 tests done at the doctor for blood and urine, all were normal results.
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetes
Andere Medikamente: Metformin ER; atorvastatin; low dose aspirin; multivitamin; magnesium; collagen peptide; CBD sublingual oil
Allergien: Typhoid vaccine
Vorherige Impfungen: Typhoid vaccine 1990s, Cardiac and respiratory distress, non-responsive for a day, in a coma.

VAERS 2493452

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: MI
Alter: 48,0
Geschlecht: F
Eingang: 29.10.2022
Impfdatum: 24.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / LA

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

Injected limb mobility decreased Injection site pain Pain Pain in extremity Paraesthesia

Symptomtext

I received the COVID vaccine at the same time as my flu vaccine. Both were in my left arm. No issues at the time, but about 24 hours after I had trouble moving my left arm and shoulder without extreme pain. I also have tingling down to my fingertips. It's possible there was an injury to the muscle at time of the vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: Due to the constant pain, I went to a HCF on 10/29/22 when I didn't see any improvement.
Aktuelle Erkrankungen: none
Vorgeschichte: thyroid
Andere Medikamente: levothyroxine 88 mcg
Allergien: none
Vorherige Impfungen: -

VAERS 2493427

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: OH
Alter: 33,0
Geschlecht: F
Eingang: 29.10.2022
Impfdatum: 26.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chest pain

Symptomtext

Patient experienced chest pain the day following her vaccination. She went to the emergency room and they ruled out any cardiac or serious issues.

Weitere VAERSDATA-Felder

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

VAERS 2490044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: WI
Alter: 26,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 20.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

Aphasia Asthenia Crying Dizziness Dysstasia Mobility decreased Pain in extremity Pyrexia

Symptomtext

Patient, (staff member at this facility) complained of severe arm pain (Rt. Arm - Booster dose given)shortly after receiving both vaccinations. Within a short amount of time she got the point where she couldn?t move it without crying. She then began feeling faint. She sat in the employee breakroom for a while. She spiked a fever of 102, got very weak to the point that she could not stand, and at one point couldn?t talk. A relative took her to the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2487397

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: -
Alter: 44,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 21.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Injected limb mobility decreased Swelling

Symptomtext

Swelling on chest above/across collar bone, extended towards right arm. Movement from shoulder to elbow was inhibited. Patient could only move right forearm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure
Andere Medikamente: Carvedilol
Allergien: Amlodipine, lisinopril, losartan
Vorherige Impfungen: Patient reports similar adverse event (swelling of chest/reduced movement of arm) following 3rd COVID-19 shot (Pfizer)

VAERS 2485596

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: NJ
Alter: 32,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 19.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Lymphadenopathy Migraine Pyrexia

Symptomtext

Patient developed fever around 2:00am next morning, migraine the following day around 2:00pm and woke up 10/21 around 7:00am with swollen armpits/lymph nodes on left side of body/arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Montelukast 10mg, Naratriptan 2.5mg, Rizatriptan ODT 10mg, Bupropion SR 100mg, Citalopram 10mg
Allergien: Eggs and shellfish
Vorherige Impfungen: -

VAERS 2484827

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: AZ
Alter: 14,0
Geschlecht: M
Eingang: 20.10.2022
Impfdatum: 20.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Feeling abnormal Loss of personal independence in daily activities Somnolence

Symptomtext

13 yo male patient received Pfizer Omicron Bivalent Booster and Flucelvax flu vaccine at 1345. Patient stated he started feeling weird after receiving the Pfizer Bivalent booster. The provider on site was alerted. Patient reported shortness of breath. The provider gave the patient Benadryl oral suspension 50 mg at 1350. at 1401, his blood pressure was 106/68, right arm manual blood pressure. His heart rate was 96 and O2 sat was 94% on room air. The patient denied swelling in his mouth but reported feeling drowsy. He denied dizziness and denied shortness of breath upon standing. His mother was notified and arranged for the patient to be picked up from school. Patient was cleared by the provider and released ambulatory to his family at 1405.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none known
Vorgeschichte: none
Andere Medikamente: none
Allergien: none known
Vorherige Impfungen: -

VAERS 2479503

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

moderat

Staat: OR
Alter: 54,0
Geschlecht: M
Eingang: 15.10.2022
Impfdatum: 08.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / RA

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

Hypoaesthesia Muscular weakness Nerve injury Paraesthesia

Symptomtext

Numbness accompanied by tingling sensation in right thumb and weakness in thumb. Feels like nerve damage. It had onset the morning after the vaccination and lasted with varying intensity for about three days. Completely resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High cholesterol
Andere Medikamente: atorvastatin, Zyrtec, fish oil, multivitamin, calcium supplement
Allergien: None
Vorherige Impfungen: -

VAERS 2478867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

moderat

Staat: OR
Alter: 86,0
Geschlecht: M
Eingang: 14.10.2022
Impfdatum: 13.10.2022
Beginn: 13.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Chills Incoherent Pain in extremity Pyrexia Tremor

Symptomtext

High fever, sore arm, chills, shaking, not coherent

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: parkinsons
Andere Medikamente: flonex, metoprolol, xarelto, omeprazole, aspira, famotidine, vitamin c, vitamin d3, fish oil
Allergien: pool chemicals
Vorherige Impfungen: Moderna 86 years

VAERS 2725575

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: AZ
Alter: 74,0
Geschlecht: F
Eingang: 19.12.2023
Impfdatum: 06.05.2023
Beginn: 07.05.2023
Tage bis Beginn: 1,0
Dosis: 6
Route/Site: IM / LA

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

Fatigue Musculoskeletal stiffness Polymyalgia rheumatica

Symptomtext

Since then she has struggled with fatigue, polymyalgia rheumatica, and stiffness.

Weitere VAERSDATA-Felder

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

VAERS 2700113

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge gj3275

mild

Staat: -
Alter: 54,0
Geschlecht: F
Eingang: 23.10.2023
Impfdatum: 20.10.2023
Beginn: 20.10.2023
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Headache Injection site pain Nausea Pyrexia Tinnitus

Symptomtext

the same evening as vaccination had tinnitus thru the night. Beginning the next afternoon ran a low grade fever (100 ish) off and on thru the next day. Also have experience some nausea and slight headache in the days since the vaccination. Sore injection site for 2 days also. Took ibuprofen for the headaches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: crestor
Allergien: valium, demerol, scallops, melons
Vorherige Impfungen: The first COVID vaccine I experienced the tinnitus for a day as well as insomnia for 2 weeks.

VAERS 2650592

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: TN
Alter: 63,0
Geschlecht: M
Eingang: 28.06.2023
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / LA

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

Dizziness Fatigue Interchange of vaccine products Pain SARS-CoV-2 test

Symptomtext

body aches; Chronic fatigue; light headed feelings; Dose 4: Moderna and dose 5: Comirnaty; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Oct2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 63 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Interstitial cystitis" (unspecified if ongoing); "BPH" (unspecified if ongoing); "mild high blood pressure" (ongoing). Concomitant medication(s) included: INFLUENZA VACCINE taken for immunisation as dose number unknown, single; ATENOLOL; FLOMAX [TAMSULOSIN HYDROCHLORIDE]; ATORVASTATIN; VITAM [ASCORBIC ACID]. Vaccination history included: coviD-19 vaccine moderna (DOSE 4 (BOOSTER), SINGLE , Lot number: 037A22B, vaccine location: Right arm), administration date: 06Jun2022, when the patient was 63-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE , Lot Number: FG3527, prev dose vaccine location: Left arm), administration date: 23Nov2021, when the patient was 62-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 2, SINGLE , Lot Number: EW0170, vaccine location: Left arm), administration date: 30Apr2021, when the patient was 62-year-old, for COVID-19 Immunization; BNT162b2 (DOSE 1, SINGLE , Lot Number: ER0734, vaccine location: Left arm), administration date: 09Apr2021, when the patient was 62-year-old, for COVID-19 Immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 28Oct2022, outcome "not recovered", described as "Dose 4: Moderna and dose 5: Comirnaty"; FATIGUE (non-serious) with onset 31Oct2022, outcome "not recovered", described as "Chronic fatigue"; PAIN (non-serious) with onset 31Oct2022, outcome "not recovered", described as "body aches"; DIZZINESS (non-serious) with onset 31Oct2022, outcome "not recovered", described as "light headed feelings". The events "body aches", "chronic fatigue" and "light headed feelings" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pain, fatigue, dizziness. Additional Information: Other vaccines were taken within 4 weeks. Other medications like antibiotics, atenolol, flomax, atorvastatin, vitamin were taken in 2 weeks. There was no treatment taken for adverse event. No known allergies. No Covid prior to vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Date: 20230220; Test Name: Home covid test; Test Result: Negative ; Comments: Nasal Swab
Aktuelle Erkrankungen: Blood pressure high
Vorgeschichte: Medical History/Concurrent Conditions: BPH; Cystitis interstitial
Andere Medikamente: INFLUENZA VACCINE; ATENOLOL; FLOMAX [TAMSULOSIN HYDROCHLORIDE]; ATORVASTATIN; VITAM [ASCORBIC ACID]
Allergien: -
Vorherige Impfungen: -

VAERS 2648360

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: AL
Alter: 70,0
Geschlecht: M
Eingang: 22.06.2023
Impfdatum: 10.12.2022
Beginn: 01.05.2023
Tage bis Beginn: 142,0
Dosis: 5
Route/Site: IM / LA

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

Cough Fatigue Hypersensitivity Laryngitis Oropharyngeal pain Pain Streptococcus test positive

Symptomtext

I had felt fatigued and achy after receiving the vaccine for about a day. In 05/2023, I had a very bad sore throat. I went to a doctor and got diagnosed with strep throat. It was really bad, and I couldn't talk. I got a prescription for an antibiotic, steroid and cough medicine. As of today, the strep throat has cleared up and I'm dealing with allergies.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: MAY2023 STREP THROAT Test - Positive
Aktuelle Erkrankungen: Seasonal Allergies
Vorgeschichte: High Cholesterol; High Blood Pressure
Andere Medikamente: Ezetimibe; Metoprolol; Losartan; Rosuvastatin; Baby Aspirin; Multivitamin; Fish Oil
Allergien: N/A
Vorherige Impfungen: -

VAERS 2639777

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MO
Alter: 69,0
Geschlecht: M
Eingang: 01.06.2023
Impfdatum: 25.11.2022
Beginn: 24.03.2023
Tage bis Beginn: 119,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Fatigue Hypersomnia Productive cough Pyrexia Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

I started to have a runny nose. 3/25 tested with at home COVID-19 test, positive. Televisit with doctor. Prescribed PAXLOVID, ADVIL, MUCINEX, and CORICIDIN D. I had a little bit of a fever and lots of fatigue. These symptoms lasted about 2 days where I mostly slept. After that, I had just a slight, periodic cough what was productive. The cough lingered about 8 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 25Mar2023 at home COVID-19 test, positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type 2 Diabetes; High Blood Pressure
Andere Medikamente: Alfuzosin; atenolol; FARXIGA; lisinopril; metformin; RESTASIS; JANUVIA; multivitamin
Allergien: Penicillin; 'sporin' family antibiotics
Vorherige Impfungen: -

VAERS 2636459

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: GA
Alter: 61,0
Geschlecht: F
Eingang: 24.05.2023
Impfdatum: 17.11.2022
Beginn: 11.05.2023
Tage bis Beginn: 175,0
Dosis: 5
Route/Site: IM / LA

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

Influenza like illness Pain Pyrexia

Symptomtext

Felt like I had the flu for a day: achy, feverish

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, Thyroid disease
Andere Medikamente: Insulin, Metformin, Synthroid, Atorvastatin, Vitamin D, Vitamin B12, Fexofenadine Hydrochloride
Allergien: Pollen
Vorherige Impfungen: -

VAERS 2636066

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: NY
Alter: 75,0
Geschlecht: F
Eingang: 24.05.2023
Impfdatum: 27.10.2022
Beginn: 14.02.2023
Tage bis Beginn: 110,0
Dosis: 5
Route/Site: IM / LA

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

Alanine aminotransferase increased Aneurysm repair Angiogram cerebral normal Angiogram normal Anticoagulant therapy Aphasia Aspartate aminotransferase increased Atelectasis Autoimmune hepatitis Blood lactic acid normal Constipation Diplopia Endotracheal intubation Headache Hepatitis viral test negative COVID-19 Chest X-ray normal Computerised tomogram abdomen

Symptomtext

2/14/2023-Presents to ED, c/o headache, aneurysm repair previous week. Blurry and double visions. Aphasia. Afebrile BO 147/91. Covid + test. CXR- no pulm disease . 95% on 4/L NC, desat to 83% on 6/L NC, intubated (40% mechanical ventilation). CT/CTA- no artery occlusion. Cerebral angio completed (robust flow to b/l PCA's). Remdesivir. 2/16/2023- Remained intubated, awake and following commands. Chest CT-small effusions and basal atelectasis. Cont on heparin gtt. Exubated. Hemo stable. WBC 11.9 afebrile but on decadron. Remdesivir d/c AST-73 ALT-91 Lipase- 466 Remains on ceftriaxone 2/18/2023- Remains on RA. Uprendng transaminase transaminitis AST 117 and ALT 124 Lipase now 857 CT abd-post/op chole clips in plac show no complications of pancreatitis. GI consult_ increase in lipase r/t constipation and UTI. bowel regimen. 2/20/2023 WBC wnl. Downtreding LFT's AST 72 and ALT 116 2/23/2023- Remains on RA. Hemo stable. WBC-9.6 ALT-137 AST -74. Lactic acid negative. Hepatitis serologies negative . Afebrile. D/c to home follow for autoimmune hepatitis outpatient basis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: 9,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Cerebral aneurysm repair, HTN, CAD w stent, A fib.
Andere Medikamente: -
Allergien: PCN
Vorherige Impfungen: -

VAERS 2635479

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: OK
Alter: 68,0
Geschlecht: F
Eingang: 23.05.2023
Impfdatum: 11.11.2022
Beginn: 21.02.2023
Tage bis Beginn: 102,0
Dosis: 5
Route/Site: IM / AR

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

COVID-19 Cough Fatigue Nasal congestion Oropharyngeal pain Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

On 2/21/2023, I developed head and nasal congestion, body aches, sore throat, cough, and fever. On 2/22/2023, I took a home antigen test and got a positive result at about 4 AM. I had a telehealth visit with my doctor later that day, and I was prescribed Paxlovid, which I began taking that day and completed taking on 2/26/2023. The Paxlovid seemed to help with the symptoms, though my fatigue persisted. On 2/27/2023, I tested negative. Aside from the persistent fatigue, I thought I was getting better. By 3/3/2023, I felt wonderful until later that evening, which is when the cough and fatigue returned. On 3/5/2023, I felt worse and had cough, nasal congestion, and fatigue. However, I had no fever. I took another test that day and got a positive result. I contacted another doctor on 3/6/2023, and the doctor told me that I had had a rebound. I was advised to isolate for five days from the onset of my symptoms and to mask for five days afterwards, which I did. I gradually got better, except the fatigue persisted for five or six weeks past the onset of the original symptoms. By the first week of April 2023, I think I was pretty much normal again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 22FEB2023 - Home Antigen Test - Positive Result; 27FEB2023 - Home Antigen Test - Negative Result; 05MAR2023 - Home Antigen Test - Positive Result
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety; Depression
Andere Medikamente: Estradiol Patch; Progesterone; Omeprazole; Meloxicam (As Needed); Zyrtec (As Needed); Tylenol (As Needed); Calcium; Multivitamin; Estradiol Vaginal Insert
Allergien: Azithromycin
Vorherige Impfungen: -

VAERS 2634895

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: ID
Alter: 75,0
Geschlecht: F
Eingang: 22.05.2023
Impfdatum: 18.11.2022
Beginn: 31.03.2023
Tage bis Beginn: 133,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Cough Ear pain Fatigue Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

On the evening of 3/31/2023, I developed a sore throat. During that night, I began coughing. On the morning of 4/1/2023, I woke up with body aches, coughing, a feeling of feverishness but no fever, and a sore throat that extended into both ears. I took a home antigen test on 4/1/2023 and got a negative result. When I took another on 4/3/2023, I got a positive result. I emailed my doctor's office and told them of the test results and the symptoms I was having. I decided not to take an antiviral, because I didn't want to experience the same side effects I had when I took PAXLOVID during my first COVID-19 infection. This time, I just treated my symptoms with ROBITUSSIN DM for the cough and TYLENOL for the sore throat and earaches. The ROBITUSSIN helped me expel some of the mucus. I also slept sitting up during this time, because I was more comfortable coughing while sitting up than I was lying down. The TYLENOL helped a little with the sore throat and earaches. My symptoms were pretty much gone after ten days. I took another home antigen test on 4/11/2023 and got a negative result. I had lingering fatigue that lasted for maybe two or three weeks after I had tested negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: 01APR2023, 11APR2023 home antigen tests, negative results; 03APR2023 home antigen test, positive result
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto's Disease; Restless Legs Syndrome; Osteoarthritis; Sjogren's Disease; Partial Block in Left Ascending Cardiac Artery (40%); Gastroesophageal Reflux Disease; Depression; Anxiety; Age-Related Macular Degeneration; Low Ferritin; Osteopenia of the Forearm
Andere Medikamente: Levothyroxine; pantoprazole; atorvastatin; pramipexole; vitamin C; ferrous sulfate; FLONASE; meloxicam; TUMS with calcium; PURITAN'S PRIDE HEALTHY EYES LUTIGOLD EXTRA; vitamin D3; sertraline; clonazepam; TYLENOL
Allergien: WELLBUTRIN; KEFLEX
Vorherige Impfungen: I had another breakthrough case after receiving my fourth dose of Pfizer COVID-19 vaccine.

VAERS 2634251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: VA
Alter: 64,0
Geschlecht: M
Eingang: 19.05.2023
Impfdatum: 11.11.2022
Beginn: 07.03.2023
Tage bis Beginn: 116,0
Dosis: 4
Route/Site: SYR / RA

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

Autoimmune disorder Erythema Feeding disorder Laboratory test Oral lichen planus Pain Stomatitis

Symptomtext

I was diagnosed with an autoimmune disease called Oral lichen planus on March 07, 2023, I was having difficulty eating, and also soreness and redness and shallow sores along my gums and teeth. I was prescribed magic mouthwash and mouth rinse.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Anti-nuclear test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2632026

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 15.05.2023
Impfdatum: 13.11.2022
Beginn: 01.03.2023
Tage bis Beginn: 108,0
Dosis: 5
Route/Site: SYR / LA

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

Arthralgia Blood test abnormal Pain Pain in extremity Red blood cell count increased

Symptomtext

The red blood count is high and it could have a stroke, I have a burning pain in my leg. I went to the doctor and they did the blood test showed the blood cells were very high. I took some vitamins and hot and cold patches to help with the knee pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 04MAY2023 Blood test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2631922

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: OH
Alter: 56,0
Geschlecht: M
Eingang: 15.05.2023
Impfdatum: 12.11.2022
Beginn: 12.04.2023
Tage bis Beginn: 151,0
Dosis: 5
Route/Site: IM / LA

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

Conjunctivitis Cough Ear discomfort Ear infection Malaise Middle ear effusion Nasopharyngitis Otorrhoea SARS-CoV-2 test negative

Symptomtext

4/12/2023 I appeared to have a severe cold. I had coughing, possible fever, pink eye and felt sick. I went to the doctor and was prescribed antibiotic drops for my eyes and a Z-Pack. I took a COVID test which was negative. Over the week-end, it moved into my left ear and I developed into an ear infection. The antibiotic did not help, but the pink eye did clear up. The ear infection, the following week, became pretty severe with drainage. I took 2 more at home COVID tests that came back negative. I went back to the doctor about a week later and was prescribed antibiotic drops for my ears and Amoxicillin. My left ear infection did clear up and I began feeling better. The ear infection may have perforated my ear which I have not fully recovered from. I went to an ENT doctor because of fluid in my ear. He said it can take a long time to go away. I still feel like I have blockage and fluid in that ear. I was given exercises to do for my ear. I still have issues with my coughing. have an appointment to go back on May 24, 2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: 13APR23-COVID Test-Negative: (?)APR23-COVID Test-Negative; (?)APR23-COVID Test-Negataive
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure , ADHD , ODC
Andere Medikamente: Lisinopril-Hydrochlorothiazide, Amphetimine-Dextroamphetimine
Allergien: None
Vorherige Impfungen: -

VAERS 2631078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MS
Alter: 51,0
Geschlecht: M
Eingang: 12.05.2023
Impfdatum: 10.11.2022
Beginn: 20.02.2023
Tage bis Beginn: 102,0
Dosis: 5
Route/Site: SYR / UN

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

Abdominal pain upper Artery dissection Computerised tomogram Dysstasia Gait disturbance

Symptomtext

My symptoms started on February 20, 2023. I was Diagnosed with Spontaneous dissection Artery I experienced pain in upper left abdomen, I had difficulty standing and walking, I was prescribed Tramadol for my pain and I was also taking Aspirin.

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Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: 4 Cat Scans
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Cholesterol
Andere Medikamente: Rosuvastatin; Vitamin D;
Allergien: N/A
Vorherige Impfungen: -

VAERS 2630565

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: OR
Alter: 65,0
Geschlecht: F
Eingang: 11.05.2023
Impfdatum: 27.10.2022
Beginn: 26.03.2023
Tage bis Beginn: 150,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Fatigue Nasal congestion Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

In March 2023 I was feeling tired and achy and had a low-grade fever. I did a video chat with my doctor and started on a 1/2 dose Paxlovid. My symptoms went away within 24 hours. I am having nasal congestion now but tested negative for COVID-19, 05/10/2023.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19, positive, 03262023
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Calcium: Vitamin D3
Allergien: N/A
Vorherige Impfungen: -

VAERS 2630543

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MO
Alter: 74,0
Geschlecht: F
Eingang: 11.05.2023
Impfdatum: 31.10.2022
Beginn: 28.03.2023
Tage bis Beginn: 148,0
Dosis: 5
Route/Site: IM / LA

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

Cough Ear pain Fatigue Respiratory tract congestion Rhinorrhoea

Symptomtext

I experienced runny nose, congestion, coughing, fatigue and ear pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Inappropriate sinus tachycardia
Andere Medikamente: Naproxen; ezetimibe; nebivolol; aspirin; pantoprazole; B complex; vitamin D3; loratadine
Allergien: Sulfa; meperidine; LIPITOR; NEURONTIN; bacitracin; fish oil
Vorherige Impfungen: -

VAERS 2627649

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MA
Alter: 52,0
Geschlecht: F
Eingang: 05.05.2023
Impfdatum: 26.10.2022
Beginn: 10.04.2023
Tage bis Beginn: 166,0
Dosis: 5
Route/Site: IM / LA

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

Abdominal pain Blood test abnormal Sensory disturbance White blood cell count increased

Symptomtext

Early in the morning on 4/10/2023, I noticed that I had abdominal pain and sensations that weren't consistent with those that accompany bowel movements (or the need to make them). The pain was still present, but not unbearable, on 4/11/2023. On 4/12/2023, the pain was still present, and I thought that I should be seen by a doctor. On that afternoon, I saw a NP. Based on the area of where the pain was concentrated, the NP thought that I could either have an ovarian cyst or diverticulitis. She then ordered a clear diet and some bloodwork. Bloodwork results indicated that my white blood cell count was high, so I was prescribed amoxicillin-clavulanic acid on 4/14/2023. I was instructed to keep the antibiotic as a standby, as the clinic would be closed for a holiday the following Monday. Overnight, from 4/14/2023 to 4/15/2023, I had abdominal pains that I would compare to those of childbirth. On 4/15/2023, I began taking the amoxicillin-clavulanic acid. By 4/16/2023, I felt much better. I continued the course of antibiotics and ate a bland diet to give my gut a chance to heal. I finished the complete course of seven days, and everything is great now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: 12APR2023 - Bloodwork - Elevated White Blood Cell Count
Aktuelle Erkrankungen: None
Vorgeschichte: Idiopathic Subglottic Stenosis; Fibromyalgia
Andere Medikamente: Lisinopril; Amlodipine; Iron; Vitamin D; Multivitamin; Garlic
Allergien: Anesthesia Sensitivity
Vorherige Impfungen: -

VAERS 2626469

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: WI
Alter: 68,0
Geschlecht: F
Eingang: 04.05.2023
Impfdatum: 29.10.2022
Beginn: 30.03.2023
Tage bis Beginn: 152,0
Dosis: 5
Route/Site: UN / UN

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

COVID-19 Cough Fatigue Respiratory tract congestion SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

I experienced a breakthrough case of COVID-19 with congestion, coughing and fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 02April2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Trazadone
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2625301

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 03.05.2023
Impfdatum: 24.10.2022
Beginn: 08.02.2023
Tage bis Beginn: 107,0
Dosis: 4
Route/Site: IM / RA

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

Dizziness Fatigue Gait inability Laboratory test Tinnitus Vertigo positional

Symptomtext

When I woke up in the morning on February 8, I felt dizzy the moment I rolled right and face down. I felt I could not walk. After a while, dizziness calmed down a little and I was able to walk. Then I went to the urgent care. I was diagnosed with "Benign paroxysmaI positional vertigo, unspecified laterality". The instructions from the doctor were to watch social media and try it several times until my issue resolves. And I got a prescription for meclizine 25mg Tab. I didn't know if the exercise was effective. I felt meclizine was a little effective. It almost healed in a few days. And I felt it completely recovered in about 2 weeks. But I felt dizzy on 04/30/2023 again. I woke up at 5:30am and went to the bathroom. At that time, I suddenly had a ringing in my ears, and I felt dizzy. When I got back to bed, my dizziness soon subsided. I took meclizine 25mg 1 Tab just in case. I didn't have any dizziness after the morning event. But I was tired that day, maybe because of the medicine. I recovered next day.

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Positional tests to check for vertigo were done on 02/08/2023. When I went from a sitting position to a lying down position, I felt dizzy.
Aktuelle Erkrankungen: none
Vorgeschichte: IgA nephropathy, High blood pressure, Hyperuricemia
Andere Medikamente: Losartan Potassium; Febuxostat.
Allergien: Iotrolan, Levofloxacin, Cefditoren Pivoxil
Vorherige Impfungen: -

VAERS 2624744

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: TX
Alter: 39,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 28.10.2022
Beginn: 21.03.2023
Tage bis Beginn: 144,0
Dosis: 4
Route/Site: SYR / LA

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

Anosmia COVID-19 Chills Cough Erythema Fatigue Lethargy Night sweats Pruritus Pyrexia SARS-CoV-2 test positive Sleep disorder Urticaria

Symptomtext

I was positive for COVID-19 on 21MAR2023, I had a fever, a lot of fatigue and I was lethargic. I was coughing and dry , I did lose my sense of smell for about 5 days. My sleep was abrupted, I had chills and night sweats. I had occasional hives on my skin in sports where it was red and itchy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 21MAR2023 COVID-19- Test- Positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: High cholesterol
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2624476

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: NH
Alter: 68,0
Geschlecht: M
Eingang: 02.05.2023
Impfdatum: 27.10.2022
Beginn: 09.03.2023
Tage bis Beginn: 133,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

My symptoms were relatively mild. A cough that got greater and greater, tiredness some congestion but not very much primarily cough.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 11MAR2023 COVID-19 Test-Positive.
Aktuelle Erkrankungen: Cold; Nasal congestion; Sesame
Vorgeschichte: Asthma; Lower backpain; Kidney stones
Andere Medikamente: Advair; Ibuprofen
Allergien: Sesame; Amoxicillin; Statins; Cipro
Vorherige Impfungen: -

VAERS 2623363

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: AZ
Alter: 63,0
Geschlecht: F
Eingang: 28.04.2023
Impfdatum: 10.12.2022
Beginn: 21.12.2022
Tage bis Beginn: 11,0
Dosis: 5
Route/Site: IM / LA

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

Chest X-ray normal Cough Fatigue Influenza A virus test negative Influenza B virus test Insomnia Lethargy Malaise Nasopharyngitis Oropharyngeal pain Pain Respiratory syncytial virus test negative Rhinorrhoea SARS-CoV-2 test negative Sneezing

Symptomtext

This started in the morning of the 12/21/2022, with a real sore throat. It felt like I had a golf ball in my throat. Severe cold symptoms: running nose, coughing, lethargy, fatigue, sneezing, headache, and body aches. sleeplessness. I tested 3 times for COVID-19 and they all came back negative every time. I tested for RSV, the results were negative. I tested for the Flu A and B and the results were negative. I tested at the Hospital for the RSV and the Flu A and B because I am in a study. December 26, 2022, I had a telehealth visit on January 16, 2023 because I was not feeling better. The first visit. I was prescribed Doxycycline for 7 days. I did not get better. January 16, 2023, I had an in person visit, they did a chest X-ray, and they gave me methylprednisolone tablet. I never fully recovered. On March 27, 2023, I got sick again. It regrouped and I went through the same symptoms again.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 28DEC2022 - RSV - negative; 28DEC2022 - Flu A and B - Negative; 23DEC2022 - Home COVID-19 Test - Negative; 27DEC2022 - Home COVID-19 Test - Negative; 29DEC2022 - Home COVID-19 Test - Negative; 16JAN2023- Chest X-ray - Normal
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Folic Acid; Hydrochlorothiazide; Valtrex; Fiber Capsules; Stool Softener; Multivitamins; Calcium; vitamin D; Potassium; Cranberry, Eye Vitamins; Magnesium; Collagen; Progesterone
Allergien: Latex; NSAIDS; High Blood Pressure That Runs in Pros, Break Out to Essential Oils
Vorherige Impfungen: -

VAERS 2622399

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: WA
Alter: 47,0
Geschlecht: F
Eingang: 27.04.2023
Impfdatum: 23.10.2022
Beginn: 23.11.2022
Tage bis Beginn: 31,0
Dosis: 4
Route/Site: SYR / UN

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

Anaemia Anal haemorrhage COVID-19 Colonoscopy abnormal Diarrhoea Headache Heavy menstrual bleeding Menstruation irregular Pain Polyp Pyrexia SARS-CoV-2 test positive

Symptomtext

I had the vaccination on 10/23/2022. On 11/23/2022 I started to experience body aches fever diarrhea and headache. I tested COVID-19 Positive on 11/23/2022. I think I have mostly recovered but I still have irregular periods since. I did have experience of heavy menstrual and anal bleeding on 11/26/2022. I was 2 weeks earlier than my regular cycle. I had an emergency colonoscopy in 11/2022. I did have some polyps. I was tested being anemic during this time.

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Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 11/23/2022 test - COVID-19 Positive; 11/2022 Blood panel
Aktuelle Erkrankungen: N/A
Vorgeschichte: Mass Cell Activation Syndrome
Andere Medikamente: Wellbutrin; Cromolyn Sodium
Allergien: Sulfa; Morphine and pain medications
Vorherige Impfungen: COVID-19 2nd and 3rd vaccination; 2021, Bells Palsy

VAERS 2620745

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: IL
Alter: 67,0
Geschlecht: F
Eingang: 25.04.2023
Impfdatum: 27.10.2022
Beginn: 28.02.2023
Tage bis Beginn: 124,0
Dosis: 5
Route/Site: IM / RA

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

COVID-19 Chills Cough Decreased appetite Fatigue Feeling abnormal Oropharyngeal pain SARS-CoV-2 test positive

Symptomtext

2/28/2023 starting that evening I had a sore throat. I woke up the next day and I was experiencing chills, fatigue, loss of appetite, and a bad cough that feels like I am choking. Tested positive with an At Home COVID-19 Test. 3/2, I had a televisit with my doctor. Doctor Proscribed Paxlovid, and an inhaler. Paxlovid was not available until 3/3. For the next 4 days, I experienced symptoms and felt bad. About a week later, I went into emergency care as I was not getting better. There I was given cough medicine and confirmed that there is no addition illness. Cough still lingers to time of reporting, though it is not as severe as previous.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 1Mar2023 At Home COVID-19 Test positive
Aktuelle Erkrankungen: NA
Vorgeschichte: Arthritis; Fibro Myalgia
Andere Medikamente: Fenofibrate; Vitamin B2; Atorvastatin; Atrovent; Vitamin D; Duloxetine; Neurontin
Allergien: NA
Vorherige Impfungen: -

VAERS 2618529

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: WI
Alter: 67,0
Geschlecht: M
Eingang: 20.04.2023
Impfdatum: 16.11.2022
Beginn: 11.02.2023
Tage bis Beginn: 87,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Cough Paranasal sinus hypersecretion Pyrexia SARS-CoV-2 test positive

Symptomtext

After my 4th dose of my Covid 19 vaccination which was Pfizer vaccination I developed a chronic cough, experienced fever and a sever case of sinus drainage. I visited the Urgent Care and was examined and diagnosed with Covid 19. I was then advised to follow up with my Primary Care physician 21 days later. I was prescribed Albuterol and Flovent.

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Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: I was tested for COVID 19 and tested positive.
Aktuelle Erkrankungen: No illnesses at the time of the vaccination.
Vorgeschichte: I currently have a chronic cough on going 8 weeks now.
Andere Medikamente: At the time of the vaccination I was taking Losartan, Bisoprolol, Omeprazole, Metamucil, Aleve. and a Fish Oil.
Allergien: No allergies to any foods or additional products.
Vorherige Impfungen: -

VAERS 2616822

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: WA
Alter: 61,0
Geschlecht: F
Eingang: 18.04.2023
Impfdatum: 26.10.2022
Beginn: 21.02.2023
Tage bis Beginn: 118,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Headache Lower respiratory tract infection Malaise Oropharyngeal pain Productive cough Pyrexia Respiratory symptom Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I had a headache at first. The next day I had a productive cough. I went to the hospital for a procedure and was tested for COVID-19 prior to my procedure as protocol and my test was positive so they sent me home and I began to feel more symptoms by the time I got home. I had a headache, sore throat, mild cough, upper respiratory symptoms like head congestion, and a fever which was around 101 degrees. The next morning I reached out to my doctors office and requested Paxlovid which I started the afternoon of the 22nd. I took Paxlovid for 5 days. I had a rebound and had a lower respiratory infection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 21FEB2023- COVID-19 PCR NAAT- Positive; 01MAR2023- COVID-19 At Home Test- Negative; 03MAR2023- COVID-19 At Home Test- Positive; 06 MAR2023- COVID-19 At Home Test- Positive; 16MAR2023 COVID-19 At Home Test- Negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Osteoarthritis; Hypertension; Hypothyroid; EOE
Andere Medikamente: Calcium Carbonate; Vitamin D; Vitamin C; Fish Oil; Vitamin B-Complex; Aspirin 81mg
Allergien: Nickle; Bee Stings; Latex
Vorherige Impfungen: -

VAERS 2616295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: LA
Alter: 61,0
Geschlecht: F
Eingang: 17.04.2023
Impfdatum: 22.11.2022
Beginn: 05.04.2023
Tage bis Beginn: 134,0
Dosis: 5
Route/Site: IM / LA

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

Dizziness Gait disturbance Gait inability Influenza virus test negative Motion sickness Respiratory syncytial virus test negative SARS-CoV-2 test positive

Symptomtext

I woke up feeling dizzy, I stumbled, I couldn't walk. I went about my day, everything was fine. Then next day it was much worse, I went to the hospital. I got tested for COVID-19 that came back negative, influenza that came back negative, RSV that came back negative. They were not sure what was causing the motion sickness, they did give me a steroid shot to help clear up any infection that may be in my body they also gave me a prescription for meclizine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 06APR2023 PCR Rapid COVID-19 -negative; 06APR2023 Influenza - negative; 06APR2023 RSV - negative
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Multivitamin
Allergien: No
Vorherige Impfungen: -

VAERS 2607490

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: PA
Alter: 76,0
Geschlecht: F
Eingang: 31.03.2023
Impfdatum: 10.11.2022
Beginn: 10.01.2023
Tage bis Beginn: 61,0
Dosis: 5
Route/Site: IM / LA

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

Abdominal discomfort COVID-19 Dizziness Fatigue Headache Influenza virus test negative Malaise SARS-CoV-2 test positive Streptococcus test negative

Symptomtext

1/10/2023 I started feeling unwell with an upset stomach and a bad headache. The next morning, 1/11/203, I was sick all over with dizziness and fatigue. I went to the clinic. I was tested for Flu, COVID, Strep. COVID was positive, Flu and Strep were negative. The doctor did not want me to take PAXLOVID due to the medications I was on. She told me to call my doctor. I called my doctor when I got home. I was prescribed methylprednisolone and azithromycin. On 1/11/23 I began taking the medications. I continued to have fatigue and dizziness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 11JAN23 COVID positive; 11JAN23 Flu, negative; 11JAN23 Strep, negative; 16JAN23 COVID at home test, positive; 18JAN23 at home COVID test, positive; 20JAN23 at home COVID test, positive; 23Jan23 at home COVID test, positive; 24Jan23 at home COVID test, negative
Aktuelle Erkrankungen: None
Vorgeschichte: Atrial Fibrillation; Dermatomyositis; Hypertension; Hashimoto's Thyroiditis
Andere Medikamente: Alendronate; digoxin; fenofibrate; folic acid; levothyroxine; methotrexate; metoprolol tartrate; prednisone; warfarin; calcium; omega 3 fish oil; vitamin D3; coQ10; red yeast rice; biotin
Allergien: None
Vorherige Impfungen: -

VAERS 2588109

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: SC
Alter: 76,0
Geschlecht: F
Eingang: 28.02.2023
Impfdatum: 20.11.2022
Beginn: 20.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / -

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

Headache Pain in extremity

Symptomtext

Bad headache; Arm hurt/ Arm pain; 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 76-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 20Nov2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 76 years for covid-19 immunisation. The patient's relevant medical history included: "Diabetic" (unspecified if ongoing), notes: Comments: Diabetic, takes medication for that.; "blood pressure" (unspecified if ongoing), notes: Takes blood pressure medication.; "She is so sensitive to medications" (unspecified if ongoing); "UTI" (unspecified if ongoing), notes: UTI and lot of times that makes it go up too. UTI which is not uncommon with being diabetic.; "Has a lot of allergic reactions, blocks out a couple of days each time for it" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: BNT162b2 (Dose 1, Single, Lot number: EL3246), administration date: 21Jan2021, for Covid-19 Immunisation, reaction(s): "Bad headache", "Dizzy", "Bone pain"; BNT162b2 (Dose 2, Single, Lot number: EL9265), administration date: 11Feb2021, for Covid-19 Immunisation, reaction(s): "Bad headache", "Dizzy", "just ached all over"; BNT162b2 (Dose 3 (Booster), Single, LOT: FF2589), administration date: 08Oct2021, for COVID-19 immunisation, reaction(s): "Headache was awful", "Sick", "hardly eat", "she could hardly move", "pain was terrible"; BNT162b2 (Dose 4 (Booster), Single, LOT: FP4554), administration date: 29Jul2022, for Covid-19 immunisation, reaction(s): "got headache", "kind of ached like she had the flu but not too bad"; Flu shot (Last fall, got flu shot but, that wasn't connected to to the other Covid vaccines.), for Flu Immunisation. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 20Nov2022, outcome "recovered", described as "Arm hurt/ Arm pain"; HEADACHE (non-serious) with onset 20Nov2022, outcome "recovered" (20Nov2022), described as "Bad headache". Therapeutic measures were taken as a result of headache. Additional information: Regarding Covid vaccines, caller stated she felt very protected. Knows that she had a lot of sensitivities to medications. Was pretty worried there would be some reaction. It was pretty strong so, she just blocked out a couple of days each time to get over it. Caller was very pleased with the vaccine. Knew there was going to be side effects. She was so sensitive to medications. Had a lot of allergic reactions, blocks out a couple of days each time for it. Patient takes medication for diabetes and blood pressure. Patient would like to know if ciprofloxacin made the blood sugar elevate. Patient had type 2 diabetic. The blood sugar levels had been more under control until the got the UTI and started ciprofloxacin. She noticed her blood sugar is elevated. She also took supplements due to her osteoporosis. Patient received the Pfizer covid vaccine as well as 3 boosters including Omicron, had really bad reactions but, did not get Covid. Mentioned other medications she had and comorbidities as well. Clarified with the caller, the details provided by the transferring agent. Reporter details: Zip Code: Provided and clarified as (Withheld). Primary / Prescribing Healthcare Professional Info: Full contact details were unknown. Was very pleased with the vaccine. Knew there was going to be side effects. She was so sensitive to medications. Ciprofloxacin: blood sugar elevated: Got really high on Friday, Saturday, Sunday, Monday and today, is not so bad. Had a UTI and a lot of times, that makes it go up too. Clarified, this started this past Friday, 17Feb2023. Outcome of event: Today, is a little high but, not too bad, is 145 today. It got really high Friday, Saturday was 198, which is very high. Sunday, was still very high, yesterday was high. Today is not as high. Clarified that it is better than when she first noticed it Friday. Treatment: Is on Rybelsus and Jardiance daily, for her blood sugar. Remembers talking to her husband and crying because one of her really good friend had just died from Covid. All she could think of was, is this what it felt like for her for those 2 weeks, this pain. Then, got Omicron booster 20Nov2022. Was at daughter's house, wanted to be around people, in case there was reaction again. Got headache, kind of ached little bit. Took Tylenol, took nap, got up, was fine, that same day, 20Nov2022. One thing, with Omicron, that she never had before was, that her arm hurt. Knows some people complain about arm pain but her arm never hurt. Never had that with any other shots, just the Omicron. Arm pain lasted a while but, wasn't debilitating or anything. Hurt for several days. Thought it was curious that she didn't have that for any of the other shots. Clarified that the arm pain started that same day that she got the Omicron booster, 20Nov2022. It was a young kid that gave it to her. The other nurses that gave it to her the other times, when they gave the vaccinations, it didn't hurt going in and didn't hurt afterward. Suspect products: Prior Vaccinations (within 4 weeks): No. Last fall, got flu shot but, that wasn't connected to the other Covid vaccines. Takes blood pressure medication. Family Medical History Relevant to Adverse Events (AEs): Daughter got the vaccine. With the second vaccine, she developed a rash that lasted, she thinks 6 moths, was pretty bad. Doctor told her not to get booster. Could not go to work because she had to have vaccine and booster in. Then, she got Covid and then she could go to work. Clarified it was the Pfizer Covid vaccine. Caller declined to complete report on daughter's experience with Covid vaccine. Adverse Events: AE required visit to: check all that apply: No. When caller asked to complete report on husband's experience, that he died after receiving Covid booster, she states ok but, does not think that had anything to do with his death. She only mentioned it because she had a friend who is an antivaxer, who was having a fit that they were getting the vaccine and the booster. She told caller the day after they took it, that it was going to kill him. Then, husband died. Neither one of them ever got Covid. Caller still wears a mask. Doctor suggested to caller that she get another booster because she is going on a trip. Since she got the last on end of Nov2022, though it wasn't necessary. Caller asks call handler if they agree with this.Caller advised to address any questions regarding any medical advice with provider. Told doctor she wasn't going to get it and agreed. Caller is very grateful for the vaccine, it was developed in a very timely manner. Knows it had been in the works a long time. People were saying it is experimental, that is so new. Wish more people had just gotten the vaccine and wore a mask, so we would not be dealing with this 3 years later. Follow-up (21Feb2023): This is a spontaneous follow-up report received from same contactable consumer. This consumer (patient) reported that: updated information included: classification added. PQC Details: Request Name: REQ-# Product: Ciprofloxacin, Verbatim Question. Inquiry: Caller would like to know if ciprofloxacin make blood sugar elevate. Caller does not have NDC# available, however confirmed that her prescription was for pills rather than injection format. DSU: Etransmitting possible duplicate AE (this report may contain additional information not shared during the warm-transfer, Reportm: #) Question: Caller would like to know if Pfizers ciprofloxacin also has drug interactions like the ciprofloxacin pills.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300077890 same product, patient, different AEs, different dose;

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Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy; Blood pressure abnormal (Takes blood pressure medication.); Diabetic (Comments: Diabetic takes medication for that.); Drug allergy; UTI (UTI and lot of times that makes it go up too. UTI which is not uncommon with being diabetic.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2586864

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: VA
Alter: 73,0
Geschlecht: M
Eingang: 24.02.2023
Impfdatum: 26.12.2022
Beginn: 02.01.2023
Tage bis Beginn: 7,0
Dosis: 5
Route/Site: IM / LA

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

Rash Rash macular Rash pruritic

Symptomtext

PATIENT REPORTED RASH ON BOTH ARMS AND LEGS AND SMALL ITCHY DOTS ON BACK.

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

VAERS 2584042

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: SC
Alter: 75,0
Geschlecht: F
Eingang: 19.02.2023
Impfdatum: 09.11.2022
Beginn: 15.11.2022
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / RA

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

Biopsy skin abnormal Eczema Rash Rash pruritic

Symptomtext

On Nov 13 both my husband and myself broke out in very itchy rash on our chest and spread to arms and legs. Spoke with Dr., he suggested allergist. Made apt. with Dr. Tested showed husband was allergy to grass and dust mites only... we saw Dermatology, prescription for topical relief. It did not work and then he did a biopsy and it showed eczema. Our question was how and why would we get eczema exact same time. We purged our home and anything that would start something like this... no relief. I believe it was the covid booster from Nov 9. We got it at the same time. We both still have the rash. And getting some relief with OTC creams....

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Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Results of December 13 Biopsy received on December 28 and were told eczema means a lot of things
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2583989

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MO
Alter: 71,0
Geschlecht: F
Eingang: 18.02.2023
Impfdatum: 23.12.2022
Beginn: 24.12.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Cough Pyrexia SARS-CoV-2 test negative

Symptomtext

Main events include fever (temporary) and a cough that has persisted from the day after the vaccine until now. She says that she has been to the ER because of her cough multiple times. Tested negative for COVID on all occations since.

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Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: Covid tests negative
Aktuelle Erkrankungen: none
Vorgeschichte: hs: Asthma, MS, Diabetes type 2, Hypertension
Andere Medikamente: unknown as she gets them via mail order
Allergien: none
Vorherige Impfungen: -

VAERS 2583304

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 17.02.2023
Impfdatum: 24.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / LA

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

Chills Headache Pyrexia

Symptomtext

rigors; headache; low grade temp; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 62-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 24Oct2022 at 12:30 as dose 5 (booster), single (Lot number: GJ3275) at the age of 62 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypertension" (unspecified if ongoing); "Obesity" (unspecified if ongoing); "elevated intraocular pressure" (unspecified if ongoing); "known allergies: Mango" (unspecified if ongoing), notes: nausea, rash; "Known allergies: lobster" (unspecified if ongoing), notes: vomit/diarrhea; "Known allergies: tetracycline" (unspecified if ongoing), notes: g.i. The patient's concomitant medications were not reported. Past drug history included: Fentanyl, reaction(s): "Drug allergy", notes: nausea/vomit/itch. Vaccination history included: BNT162b2 (DOSE 4 (BOOSTER), Vaccine administration time=09:30 AM, Vaccine lot number=FK9894, Vaccine location=Left arm), administration date: 08Apr2022, when the patient was 62-year-old, for COVID-19 IMMUNIZATION; BNT162b2 (DOSE 3 (BOOSTER), Vaccine administration time=04:00 PM, Vaccine lot number=CJ511-06, Vaccine location=Left arm), administration date: 05Oct2021, when the patient was 61-year-old, for COVID-19 IMMUNIZATION; BNT162b2 (DOSE 2, Vaccine administration time=11:45 AM, Vaccine lot number=EL3246, Vaccine location=Left arm), administration date: 14Jan2021, when the patient was 61-year-old, for COVID-19 IMMUNIZATION; BNT162b2 (DOSE 1, Vaccine lot number=EH9899, Vaccine location=Left arm), administration date: 22Dec2020, when the patient was 60-year-old, for COVID-19 IMMUNIZATION. The following information was reported: CHILLS (non-serious), outcome "unknown", described as "rigors"; HEADACHE (non-serious), outcome "unknown"; PYREXIA (non-serious), outcome "unknown", described as "low grade temp". Patient got rigors/headache/low grade temp reaction after Covid vaccinations, which were severe enough that she scheduled time off work.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to antibiotic (g.i.); Food allergy (vomit/diarrhea); Fruit allergy (nausea, rash); Hypertension; Intraocular pressure increased; Obesity
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2582947

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: PA
Alter: 26,0
Geschlecht: F
Eingang: 16.02.2023
Impfdatum: 14.11.2022
Beginn: 16.11.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Rash Urticaria

Symptomtext

I got a hive like rash on my right arm, hand, abdomen, back and my left side of my back. I went to the doctor, and she said it could be because of the COVID-19 vaccine. She prescribed me prednisone and my rash was almost completely gone in 3 days. I contacted my primary doctor, and she said not to get a COVID-19 vaccine again.

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Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Slight cold
Vorgeschichte: Anemic
Andere Medikamente: Amitriptyline; iron
Allergien: Bee venom
Vorherige Impfungen: -

VAERS 2582291

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MD
Alter: 55,0
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 15.11.2022
Beginn: 26.12.2022
Tage bis Beginn: 41,0
Dosis: 4
Route/Site: SYR / RA

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

COVID-19 Cough Fatigue Illness Influenza virus test negative Nasal congestion Pain in jaw Pyrexia SARS-CoV-2 test positive Sinus pain Toothache

Symptomtext

On December 26, 2022, I had a fever of 104-degrees. I had a fever on and off for a few weeks after that averaged 101-degrees. I was tested for COVID-19 and Flu. Both tests came back negative. The illness lasted for about a month. It included severe sinus pain, a lot of jaw and tooth pain, significant nasal congestion, and a horrible cough. I was also very fatigued. I treated it with TYLENOL and MUCINEX. I saw my doctor. She prescribed doxycycline. That was almost two weeks after my symptoms started. The fevers ended, but the other symptoms lasted for about a month. On February 6, 2023, I contracted COVID-19. I called the doctor. I was offered PAXLOVID, but I decided not to take it. They symptoms resolved in about a week.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 12/2022 COVID-19 test negative; 12/2022 Flu test negative; 02/2023 COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Borderline Hypertension
Andere Medikamente: Spironolactone; turmeric; calcium; coQ10; fish oil; turkey tail mushrooms; agarikon mushrooms; vitamin C; cinnamon; lactobacillus; vitamin D3; niacin
Allergien: Strawberries; kiwi; penicillin; erythromycin; sulfite sensitivity
Vorherige Impfungen: -

VAERS 2580969

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: OR
Alter: 63,0
Geschlecht: F
Eingang: 13.02.2023
Impfdatum: 07.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 3,0
Dosis: N/A
Route/Site: UN / LA

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

Arthritis Pain Synovial cyst X-ray

Symptomtext

Severe inflammation of arthritis in right knee joint and surrounding areas/tissues, including Baker's Cyst. Physical therapy sessions (6) since then has helped, but I have not reached total pain resolution yet.

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Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: 11/16/2022 xray. 11/2382022 Urgent Care Visit because other Urgent care was "at capacity" and I was sent out of network. 12/9/2022 recheck with primary care physician.
Aktuelle Erkrankungen: posterior vitreous detachment
Vorgeschichte: asthma, osteoarthritis
Andere Medikamente: gabapentin, rosuvastatin, venlafaxine, alvesco, albuterol, losartan
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2580458

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: NJ
Alter: 67,0
Geschlecht: F
Eingang: 13.02.2023
Impfdatum: 11.11.2022
Beginn: 17.01.2023
Tage bis Beginn: 67,0
Dosis: 5
Route/Site: UN / LA

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

Headache Productive cough Pyrexia

Symptomtext

Headache - approximately 2-3 days productive cough - ongoing fever - 1 day Doctor prescribed: Albuterol Sulfate HFA 108 (90 Bae) MCG/ACT - 4 times a day as needed for cough/ wheezing or chest tightness Paxlovid (300/100) 20 x 150 MG & 10 x 100 MG

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Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Amlodipine Besylate Simvastatin Wixella (Flutcasone propionate 250 mcg and salmetero 50 mcg)
Allergien: None
Vorherige Impfungen: Swollen lymph nodes under left arm.

VAERS 2579578

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CT
Alter: 39,0
Geschlecht: F
Eingang: 10.02.2023
Impfdatum: 10.11.2022
Beginn: 15.01.2023
Tage bis Beginn: 66,0
Dosis: 4
Route/Site: SYR / LA

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

Arthralgia COVID-19 Cough Fatigue Feeling abnormal Feeling hot Headache Oropharyngeal pain Pain in extremity Parosmia Peripheral swelling Respiratory tract congestion SARS-CoV-2 test positive Secretion discharge Tenderness

Symptomtext

I had a sore arm after the vaccines, swelling and very tender and hot. I was also fatigued and had a headache. All of these lasted between 24 hours to 48 hrs. The soreness of my arm lasted a few days. In January I contracted COVID. I experienced cough which I still have and I noticed the most. I also had fatigue which started about a day or 2 after which is why I tested myself because it was severe fatigue. I tested myself positive. By the 15th of January, so around a day after, I had a sore throat and mucus and congestion. I could not smell things with a mild smell but things like coffee that had a strong smell I could still smell. I had a bit of brain fog but it did not last long. I also had achy joints for about a week. By the 20th of January I saw the doctor and he prescribed I take some over the counter medication and prescribed advere discus. I took around 8 doses. Today, Feburary 10th, I still have a bit of mucus which is still making me cough, but nothing else.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: COVID Home test
Aktuelle Erkrankungen: None
Vorgeschichte: migraines; restless leg syndrome; anxiety; depression
Andere Medikamente: Lexapro; gabapentin; Copamex; ataman; vitamin D; Maxalt
Allergien: sulfa drugs; penicillin; doxycycline; ciprofloxacin;
Vorherige Impfungen: -

VAERS 2576580

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

mild

Staat: NM
Alter: 81,0
Geschlecht: M
Eingang: 06.02.2023
Impfdatum: 07.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / RA

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

Myalgia

Symptomtext

continued soreness as if was given vaccine yesterday. Has not noticed any improvement. No redness, swelling, or hot to touch just muscle soreness as expected after vaccine however not continued for months post vaccine.

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Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: none encouraged pt to be evaluated by physician
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2576555

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: NY
Alter: 50,0
Geschlecht: F
Eingang: 06.02.2023
Impfdatum: 04.11.2022
Beginn: 01.01.2023
Tage bis Beginn: 58,0
Dosis: 5
Route/Site: IM / RA

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

Arthralgia Blood test abnormal Contusion Dry skin Fatigue Insomnia Massage Pruritus Psoriasis Urticaria

Symptomtext

I developed hives and itchiness all over the body excluding my face. They lasted for 3 weeks. The hives lasted for 2 weeks. I had poison ivy level itchiness which caused it to be difficult to sleep. I saw my doctor around the 2nd week of January. She prescribed prednisone after I had taken BENADRYL all weekend and showered with SELSUN BLUE. The itching was so bad that I developed black and blue bruises on my legs, arms, and back. I had had a massage and thought that it could be the massage oil. I took the prednisone, and it didn't help. I was using more steroids and removed spicy foods from my diet. I was only able to wear very soft loose clothing. I was advised not to drink alcohol. I was on the prednisone for 10 days and I was advised not to do any activities that would cause me to sweat and irritate the rash. My knees were so painful I wanted to cry. I took oatmeal baths and psoriasis. I used eczema creams as well. It didn't go away until last week. All the symptoms subsided except for a little dry skin. I am still very tired as well.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Blood panel drawn previously unrelated, date will be shared with provider since it was recent. Results unknown as results are under review 11-2022
Aktuelle Erkrankungen: Cold
Vorgeschichte: Lyme Disease; Cold sores-mouth
Andere Medikamente: LEXAPRO; gabapentin; vitamin; METHY-PROTECT; adenosyl hydroxy B12; COLON X; 3A magnesia; daily multivitamin; IMN-V DROP; DIM DETOX; zinc somaplex; coQ10 power; tri salts; OMEGA BENEFIT; ROSAVIN; THYRO-CARE; S-acetyl-glutathione; vitamin D3-
Allergien: Dust mites; cat hair
Vorherige Impfungen: -

VAERS 2575057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: OH
Alter: 35,0
Geschlecht: F
Eingang: 03.02.2023
Impfdatum: 25.10.2022
Beginn: 01.12.2022
Tage bis Beginn: 37,0
Dosis: 4
Route/Site: IM / RA

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

Arthralgia Autoimmune disorder Blood test abnormal Echocardiogram abnormal Laboratory test

Symptomtext

I went to doctor in December, my joints hurt, and did a lot of tests, they sent me to Cardiologist, I went back in January, and they detected an auto immune, and due to the Echo results the doctor sent me to the cardiologist, I still have to go to see him.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: 12Dec2022 Blood test, abnormal; 09JAN2023 ECHO, abnormal
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Penicillin; sulfa
Vorherige Impfungen: COVID-19 dose 1, dose 2, 3 dose

VAERS 2574236

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: AZ
Alter: 69,0
Geschlecht: F
Eingang: 02.02.2023
Impfdatum: 02.11.2022
Beginn: 16.01.2023
Tage bis Beginn: 75,0
Dosis: 5
Route/Site: UN / UN

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

Ageusia Anosmia Facial pain Respiratory tract congestion Sinus disorder

Symptomtext

I experienced congestion, facial pain, sinuses and loss of taste/smell.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Blood pressure
Andere Medikamente: Olmesartan
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2572332

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

mild

Staat: MI
Alter: 55,0
Geschlecht: F
Eingang: 31.01.2023
Impfdatum: 01.11.2022
Beginn: 31.01.2023
Tage bis Beginn: 91,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Back pain Hypoaesthesia Pain Pain in extremity

Symptomtext

pain started in shoulder, didnt go away and started radiating to back and fingers. hands get numb even when holding the phone. steroids did not help

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: none starting PT soon
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroidism
Andere Medikamente: synthroid medrol dose pack taken early january for the pain to try to treat
Allergien: nkda
Vorherige Impfungen: -

VAERS 2572085

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: VA
Alter: 35,0
Geschlecht: M
Eingang: 31.01.2023
Impfdatum: 29.10.2022
Beginn: 08.01.2023
Tage bis Beginn: 71,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Cough Fatigue Headache Oropharyngeal pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

It started with a sore throat on day one and progressed with fever headache fatigue then it went to congestion and cough all other symptoms had resolved by day seven or eight but mild cough still remains.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 at home test positive, then negative on day twelve or thirteen.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2568670

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 26.01.2023
Impfdatum: 17.12.2022
Beginn: 29.12.2022
Tage bis Beginn: 12,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Pyrexia SARS-CoV-2 test positive

Symptomtext

12/29/22 presents to ED for "fever". PMHx of "CKD stage III, hypertension and DVT on anticoagulation"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 12/29/22 SARS-CoV-2 (COVID-19) detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2567617

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: PA
Alter: 79,0
Geschlecht: F
Eingang: 25.01.2023
Impfdatum: 13.12.2022
Beginn: 14.12.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: SYR / LA

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

Erythema Pruritus

Symptomtext

After the next day when I woke up I started getting itchy and got worse and worse. I do have a picture of it. My back was all red, It only stayed in that area. I was going to physical therapy to use heat lamp for cirrhosis. I would never take another shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Blood pressure pills atenolol lisinopril meloxicam
Allergien: sulfa drug
Vorherige Impfungen: 2nd shot of COVID PFIZER I started to get a rash.

VAERS 2566838

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: WI
Alter: 59,0
Geschlecht: F
Eingang: 24.01.2023
Impfdatum: 24.10.2022
Beginn: 11.12.2022
Tage bis Beginn: 48,0
Dosis: 5
Route/Site: IM / LA

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

Ear discomfort Ear infection Headache Increased upper airway secretion Malaise Oropharyngeal pain Pain in extremity Rhinorrhoea Sinusitis

Symptomtext

I had a sore arm for a couple of days and that was it. I started not feeling well on 12/11/2022 I had a runny nose and sore throat. It was progressed to fullness in the ears, headache and runny nose. I went to an urgent care and was diagnosed with a sinus infection and double ear infection. I was prescribed prednisone for my symptoms. I tolerated the medication. As of today, I still have drainage in the back of throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Fibromyalgia
Andere Medikamente: N/A
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2564995

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: MI
Alter: 45,0
Geschlecht: M
Eingang: 21.01.2023
Impfdatum: 11.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Arthralgia Joint range of motion decreased Periarthritis

Symptomtext

frozen shoulder; Adhesive capsulitis of left shoulder; decreased range of motion in left shoulder shortly after injection, followed by pain in same shoulder; decreased range of motion in left shoulder shortly after injection, followed by pain in same shoulder; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 11Nov2022 as dose number unknown (booster), single (Lot number: GJ3275) at the age of 45 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 immunization. The following information was reported: PERIARTHRITIS (non-serious) with onset 11Nov2022, outcome "unknown", described as "Adhesive capsulitis of left shoulder"; JOINT RANGE OF MOTION DECREASED (non-serious), ARTHRALGIA (non-serious) all with onset 11Nov2022, outcome "unknown" and all described as "decreased range of motion in left shoulder shortly after injection, followed by pain in same shoulder"; PERIARTHRITIS (non-serious) with onset 17Jan2023, outcome "unknown", described as "frozen shoulder". The events "adhesive capsulitis of left shoulder", "decreased range of motion in left shoulder shortly after injection, followed by pain in same shoulder" and "frozen shoulder" required physician office visit. Therapeutic measures were taken as a result of periarthritis, joint range of motion decreased, arthralgia, periarthritis. Additional information: Started experiencing decreased range of motion in left shoulder shortly after injection, followed by pain in same shoulder. After self-treatment for a couple of months, sought treatment by orthopedic surgeon who ordered physical therapy. PT discussed causes which vaccines could be a cause for frozen shoulder and timing matched up. This was discovered on 17Jan2023 around 12pm. Event took place after use of product.

Weitere VAERSDATA-Felder

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

VAERS 2563309

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: SD
Alter: 55,0
Geschlecht: F
Eingang: 19.01.2023
Impfdatum: 19.10.2022
Beginn: 27.12.2022
Tage bis Beginn: 69,0
Dosis: 4
Route/Site: SYR / LA

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

Abdominal discomfort COVID-19 Fatigue Headache Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I received my Covid-19 vaccine on 10/19/2022. On 12/27/2022 I woke up with a headache and fatigue. Next day my headache gotten worse and with a sore throat, congestion and upset stomach. I took a home Covid test and was positive. I contacted my doctor and was prescribed Paxlovid. Symptoms lasted a couple days with ongoing congestion issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2562373

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: VA
Alter: 46,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 01.11.2022
Beginn: 01.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: SYR / LA

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

Arthritis Blood test normal Headache Joint swelling Magnetic resonance imaging normal Muscle spasms Muscle twitching X-ray abnormal

Symptomtext

Since receiving COVID-19 vaccines, has been having ongoing joint inflammation and swelling; After this Bivalent vaccine symptoms have become worse also include low grade headaches and started having muscle spasms and twitching; Has been seeing various doctors to find a diagnosis; Has a Neurology appointment next month.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Multiple Blood Panels, negative findings; MRI, negative finding; X-ray of the joints, inflammation.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Clindamycin; amoxicillin.
Vorherige Impfungen: -

VAERS 2561951

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: IL
Alter: 52,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 13.01.2023
Beginn: 14.01.2023
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Injection site erythema Injection site pain Injection site reaction Muscle discomfort Muscle tightness

Symptomtext

Patient received the Pfizer Bivalent shot at our pharmacy on 1/13/2023, around 5.45 pm. She developed redness , pain under the injection site . Redness was spreading down to bicep & around with fullness & tightness when the time goes. She spoke to her Doctor office & started taking Cephalexin & Advil per Doctor instruction. She has appointment tomorrow(1/18/23) to see her Doctor. Advil helps her for the pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None except She spoke to her office and will be seeing the Doctor on 1/18/23
Aktuelle Erkrankungen: NOTING SIGNIFICANT
Vorgeschichte: ANXIETY & RELATED HORMONE & RELATED
Andere Medikamente: OMEPRAZOLE 20 MG SERTRALINE 25 MG TAMOXIFEN 20 MG
Allergien: IODIDE PENICILLIN TETRACYCLINE & RELATED
Vorherige Impfungen: -

VAERS 2561356

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 17.01.2023
Impfdatum: 02.01.2023
Beginn: 07.01.2023
Tage bis Beginn: 5,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Decreased appetite Diarrhoea Dizziness Fatigue Feeling abnormal Gastrointestinal disorder Gastrointestinal pain Influenza virus test negative Insomnia Nasopharyngitis Pregnancy test negative SARS-CoV-2 test positive Vomiting

Symptomtext

I started having cold symptoms on 01/07/2023. I tested negative for COVID-19 at that time, but I didn't realize the test had expired. I began having extreme gastrointestinal issues on 01/11/2023 and went to an urgent care clinic where I was diagnosed with COVID-19 on 01/12/2023. On 01/11/2023, I woke up with extreme gastrointestinal pain at around 03:00AM. I was feeling it through my entire torso. I was able to use the bathroom a few times, but the stool was loose and did not provide any relief. Around 06:00AM, I vomited. From 01/11/2023-01/14/2023, the extreme gastrointestinal pain continued, and I had extreme fatigue. I have maintained my taste and smell but have no appetite. My bathroom activity has diminished. Every time I use the bathroom it doesn't feel like as much as it should be based on what I'm taking in. I'm still having gastrointestinal pain, but it is diminished. I also continue to have fatigue. I have been experiencing a brain fog since receiving my vaccine on 01/02/2023. It seems to be getting better. For the most part, my sleep issues have improved but are not resolved. Some nights I sleep soundly and then the next night I'll have insomnia. I have been treating my stomach issues with PEPCID which provides modest improvement. Beginning on 01/11/2023 I also experienced dizziness that has been improving over time and feels mostly resolved at this point.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 08JAN2023 at home COVID-19 negative; 12JAN2023 rapid COVID-19 test positive; Flu test negative; Pregnancy test negative; 16JAN2023 at home COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure; Nasal Allergies; Asthma; Obesity
Andere Medikamente: Hydrochlorothiazide; valsartan; montelukast; BREZTRI; multivitamin
Allergien: Severe nasal allergies; AUGMENTIN
Vorherige Impfungen: -

VAERS 2560790

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: FL
Alter: 76,0
Geschlecht: M
Eingang: 16.01.2023
Impfdatum: 27.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Injection site pain Myalgia

Symptomtext

Site: Pain at Injection Site-Mild, Additional Details: Patient reports pain in left arm at the injection site that has persisted ever since getting the Pfizer booster vaccine on 10/27/2022. "Dull muscle pain"

Weitere VAERSDATA-Felder

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

VAERS 2558602

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: AZ
Alter: 38,0
Geschlecht: F
Eingang: 12.01.2023
Impfdatum: 12.10.2022
Beginn: 22.12.2022
Tage bis Beginn: 71,0
Dosis: 4
Route/Site: SYR / AR

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

Conjunctivitis Cough Ear infection Fatigue Headache Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test negative Sinusitis

Symptomtext

On Thursday, December 22, 2022, I had a sore throat, cough, and congestion. I consulted on online doctor who gave some advice but did not provide medication. The symptoms worsened through December 25th and 26th to included headache and fatigue. I went to urgent care on December 26, 2022. The provider administered a COVID-19 test. The result was negative. I was diagnosed with an ear infection, a sinus infection, and conjunctivitis. The cough and congestion continued until about January 5 or 6, 2023. Minor sinus symptoms continued through January 12, 2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 12/26/2022 COVID-19 Test - Negative
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; Obesity; Migraines; Depression
Andere Medikamente: Zyrtec; Melatonin; Guanidine; Oxybutynin Chloride; Sertraline; Labetalol; Vitamin D; Multivitamin
Allergien: Pollen; Amoxycillin; Chlorhexidine
Vorherige Impfungen: -

VAERS 2556876

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 21.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Arthralgia

Symptomtext

Systemic: claims shoulder pain 2 months after shot-Mild, Additional Details: Patient received shot on 10/21/22, recently had a doctors appointment and is having shoulder discomfort. Doctor told her "dont know" what shoulder issue is from. Call the pharmacy" Over 2 months after shot, its being reported to us.

Weitere VAERSDATA-Felder

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

VAERS 2556104

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CO
Alter: 57,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 26.12.2022
Beginn: 05.01.2023
Tage bis Beginn: 10,0
Dosis: UNK
Route/Site: IM / LA

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

COVID-19 Loss of personal independence in daily activities Periorbital pain Periorbital swelling Rhinalgia Rhinorrhoea SARS-CoV-2 test positive Sinus pain

Symptomtext

I received the Pfizer Bivalent COVID-19 booster on 12/26/2022. On 1/5/2023, I began having pain inside the left nostril, which intensified to the point at which I couldn't wash or touch my face. I thought that maybe I had a pimple inside the nose, because the pain was concentrated in one spot. By 1/6/2023, though, the pain had spread throughout the left side of the nose, and I had pain and a little bit of swelling under the left eye. It felt like a sinus infection. On 1/8/2023, I still had pain on the left side of my nose, but then my nose started to run out of both nostrils. I then took a home antigen test, and the result was positive. I was surprised by this, so I took another test that day to see if I would get the same result, and the second test also yielded a positive result. Later that day, I had a virtual urgent care visit, and I was prescribed PAXLOVID, which I began taking that evening. It began to work quickly. The pain in the left side of my nose began to subside on 1/9/2023. At the time of this writing, I also no longer have a runny nose. Since getting COVID-19, I have had no symptoms besides the sinus pain on the left side, the slight swelling under the left eye, and the runny nose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Periorbital pain
Hospital-Tage: -
Labordaten: 2 home antigen tests 1/8/2023 positive results.
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypertension.
Andere Medikamente: CENTRUM multivitamins; levothyroxine; metoprolol.
Allergien: Penicillin; iodine; contrast dye; tree pollen; neomycin.
Vorherige Impfungen: -

VAERS 2553216

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CA
Alter: 35,0
Geschlecht: M
Eingang: 07.01.2023
Impfdatum: 06.01.2023
Beginn: 07.01.2023
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Anxiety Asthenia Chills Headache Heart rate increased Musculoskeletal stiffness Pain Pyrexia

Symptomtext

I went to sleep feeling fine. Awoke at 4 am with Chills, fever, weakness, body aches every where, stiff neck, and anxiety. My heart feels like it?s beating really fast. I have the worst headache I?ve ever had in my life.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None yet.
Aktuelle Erkrankungen: None
Vorgeschichte: Alpha-1 Antitrypsin Deficiency (Heterozygous) Non-alcoholic Fatty Liver disease from Alpha-1 Asthma Survivor of long-term, low-exposure carbon monoxide poisoning (almost 3 years of exposure).
Andere Medikamente: PRN Clonazopam, Gabapentin, Adderall, Seroquel
Allergien: None
Vorherige Impfungen: -

VAERS 2552607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: TX
Alter: 59,0
Geschlecht: F
Eingang: 06.01.2023
Impfdatum: 02.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 8,0
Dosis: 4
Route/Site: SYR / RA

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

Blood test normal Nausea Parosmia Vomiting

Symptomtext

Have started to constantly smell cigarettes; The smell has led to me being nauseous and vomiting; My doctor drew a blood panel but didn't find any cause.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: High blood pressure; High Cholesterol; Osteoporosis
Andere Medikamente: Lisinopril; REPATHA injection; ZYRTEC; multivitamin; joint support supplement
Allergien: Red food dye; VICODIN; all blood pressure medications; all high cholesterol medications
Vorherige Impfungen: -

VAERS 2551500

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 01.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 3,0
Dosis: 5
Route/Site: IM / LA

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

Injection site pain Myalgia Pain

Symptomtext

very mild typical arm soreness at injection site for few days after injection, then noticeable and increasing deep muscle (brachialis) pain during movement. has not decreased after 2 months,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: asthma (COPD)/ hypothyrodism
Andere Medikamente: Levothyroxine 137mg Hydrochlythorizide 25mg Albuterol inhaler as needed
Allergien: various HBP medications
Vorherige Impfungen: -

VAERS 2549078

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MD
Alter: 59,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 29.12.2022
Beginn: 30.12.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Pain in extremity Peripheral swelling

Symptomtext

Pt reported swollen arm and pain still present 5 days later (1/3) though improving. Unable to tell is red.

Weitere VAERSDATA-Felder

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

VAERS 2548859

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: PA
Alter: 74,0
Geschlecht: F
Eingang: 03.01.2023
Impfdatum: 30.12.2022
Beginn: 30.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Dizziness Malaise

Symptomtext

Patient was given the Covid Vaccine Booster. She was asked to wait 15 minutes after the vaccine. After 5 minutes patient and her son reported that she was feeling dizzy and unwell. Pharmacist assured the patient is getting the proper treatment. The pharmacist asked if the patient if she likes to the hospital and she replied yes. The pharmacist had both patient and her son sit down while made the call. The paramedics came and took the patient to the hospital of her choice.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Not sure.
Aktuelle Erkrankungen: Insomnia Dizziness Acid reflux
Vorgeschichte: Anxiety/Depression
Andere Medikamente: Mirtazapine, Meclizine, Omeprazole,
Allergien: No known drug allergies
Vorherige Impfungen: -

VAERS 2544772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MO
Alter: 5,0
Geschlecht: M
Eingang: 28.12.2022
Impfdatum: 10.12.2022
Beginn: 10.12.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Ear pain Oropharyngeal pain Otitis externa Pruritus Pyrexia Secretion discharge Urticaria Viral infection Vomiting

Symptomtext

I honestly think these two things may have just happened at the same time. A few hours after receiving his vaccine on 12/10/2022, he developed a 103-degree fever that night. The next morning, he was complaining of an earache. We took him to a local hospital where they diagnosed swimmer's ear and prescribed medicine. That Tuesday, I realized his throat was hurting because he was only wanting to eat popsicles. That night, he had a vomit with mucus. That Thursday, he was itching and broke out in hives. That Friday, we went to see his physician who stated that he had a virus that resulted in hives and recommended we treat the hives. We gave him BENADRYL for around three days and the hives went away and he has been fine since then.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Cold like symptoms
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2543276

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

mild

Staat: CA
Alter: 81,0
Geschlecht: U
Eingang: 26.12.2022
Impfdatum: 21.12.2022
Beginn: 22.12.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Asthenia Cold sweat Decreased appetite Diarrhoea Fatigue Fluid intake reduced Pain

Symptomtext

Patient states feeling achy the next day. Patient cannot confirm if patient has a fever. In addition, patient states having diarrhea and cold sweat since one day post vaccination until today/now (12/22/22 to 12/26/22). Patient states feeling very tired/weak and unable to eat or drink normal amount of fluids (today patient had a cup of Jello and 1/2 bottle of water). Patient took 1 dose of OTC pepto bismol. Due to patient's age, duration of diarrhea and decreased fluid/food intake, pharmacist advised for patient to seek urgent care. Patient states waiting for advice nurse to call back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN and others (please check with patient)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2537245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: CA
Alter: -
Geschlecht: M
Eingang: 23.12.2022
Impfdatum: 08.12.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / -

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

Pain in extremity

Symptomtext

soreness of arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 08Dec2022 at 17:00 as dose 5 (booster), single (Lot number: GJ3275), in arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: EN6199, Time: 1st two were at 11:00, before noon), administration date: 06Mar2021, for Covid-19 Immunization, reaction(s): "Soreness of right arm after each injection 1-4"; BNT162b2 (DOSE 2, SINGLE; Lot number: EP6955, Time: 1st two were at 11:00, before noon), administration date: 27Mar2021, for Covid-19 Immunization, reaction(s): "Soreness of right arm after each injection 1-4"; BNT162b2 (Dose 3(Booster), Lot 301558A, 3rd was done around 13:00), administration date: 20Oct2021, for Covid-19 Immunization, reaction(s): "after the 3rd dose, both of them experiences soreness/Soreness of right arm after each injection 1-4/both had arm soreness after each injection, not just the 3rd dose"; BNT162b2 (Dose 4(Booster), Lot FJ4989, 4th one that had issue with unknown time and), administration date: 14Apr2022, for Covid-19 Immunization, reaction(s): "soreness of arm", "soreness of arm". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 2022, outcome "recovered" (2022), described as "soreness of arm". Therapeutic measures were not taken as a result of pain in extremity. Additional information: Did mention both had series of Pfizer COVID vaccine injections 5 injections total. Both of them, after 3rd dose, they had soreness of arm that went away after 3 to 4 days. He said they both had arm soreness after each injection, not just the 3rd dose. Each time they had injection they had soreness of arm. All soreness started the evening of the injection, and really noticed it the next day. Eventually in a couple or 3 days, the soreness was gone. They did not want Moderna, so all of them were Pfizer. Both of them received their vaccines on the same dates, times, locations, with the exact same lot numbers for all. Family Medical History Relevant to Adverse Events (AEs): none.; Sender's Comments: Linked Report(s) : PFIZER INC-PV202200128272 same reporter/patient/drug/AE, different dose;

Weitere VAERSDATA-Felder

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

VAERS 2537245

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: CA
Alter: -
Geschlecht: M
Eingang: 23.12.2022
Impfdatum: 08.12.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / RA

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

Pain in extremity

Symptomtext

soreness of arm; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 08Dec2022 at 17:00 as dose 5 (booster), single (Lot number: GJ3275), in arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: EN6199, Time: 1st two were at 11:00, before noon), administration date: 06Mar2021, for Covid-19 Immunization, reaction(s): "Soreness of right arm after each injection 1-4"; BNT162b2 (DOSE 2, SINGLE; Lot number: EP6955, Time: 1st two were at 11:00, before noon), administration date: 27Mar2021, for Covid-19 Immunization, reaction(s): "Soreness of right arm after each injection 1-4"; BNT162b2 (Dose 3(Booster), Lot 301558A, 3rd was done around 13:00), administration date: 20Oct2021, for Covid-19 Immunization, reaction(s): "after the 3rd dose, both of them experiences soreness/Soreness of right arm after each injection 1-4/both had arm soreness after each injection, not just the 3rd dose"; BNT162b2 (Dose 4(Booster), Lot FJ4989, 4th one that had issue with unknown time and), administration date: 14Apr2022, for Covid-19 Immunization, reaction(s): "soreness of arm", "soreness of arm". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 2022, outcome "recovered" (2022), described as "soreness of arm". Therapeutic measures were not taken as a result of pain in extremity. Additional information: Did mention both had series of Pfizer COVID vaccine injections 5 injections total. Both of them, after 3rd dose, they had soreness of arm that went away after 3 to 4 days. He said they both had arm soreness after each injection, not just the 3rd dose. Each time they had injection they had soreness of arm. All soreness started the evening of the injection, and really noticed it the next day. Eventually in a couple or 3 days, the soreness was gone. They did not want Moderna, so all of them were Pfizer. Both of them received their vaccines on the same dates, times, locations, with the exact same lot numbers for all. Family Medical History Relevant to Adverse Events (AEs): none.; Sender's Comments: Linked Report(s) : PFIZER INC-PV202200128272 same reporter/patient/drug/AE, different dose;

Weitere VAERSDATA-Felder

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

VAERS 2536802

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: TX
Alter: 66,0
Geschlecht: M
Eingang: 19.12.2022
Impfdatum: 11.11.2022
Beginn: 12.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Pain in extremity

Symptomtext

Patient came in and stated arm had started hurting day after receiving the vaccine. Informed patient that pain could last for a few months and to take tylenol or ibuprofen to help with pain in the main time. Pt stated with follow-up with dr just to make sure.

Weitere VAERSDATA-Felder

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

VAERS 2535393

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CO
Alter: 65,0
Geschlecht: F
Eingang: 16.12.2022
Impfdatum: 28.10.2022
Beginn: 29.11.2022
Tage bis Beginn: 32,0
Dosis: 4
Route/Site: IM / RA

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

Balance disorder Dizziness Fatigue Headache Pain Respiratory tract congestion SARS-CoV-2 test Tendonitis

Symptomtext

I had deep chest congestion. Strong body aches with a mild headache. Weakness and very fatigue. Still experiencing fatigue and some dizziness lately, balance issues. I got tendinous really bad.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: At home rapid COVID-19 test
Aktuelle Erkrankungen: No
Vorgeschichte: High blood pressure
Andere Medikamente: Amlodipine; TYLENOL
Allergien: No
Vorherige Impfungen: -

VAERS 2535157

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

mild

Staat: NY
Alter: 26,0
Geschlecht: F
Eingang: 16.12.2022
Impfdatum: 15.12.2022
Beginn: 15.12.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Injection site rash Rash Rash erythematous Rash pruritic

Symptomtext

pt got itchy small red bumps all over both arms and neck and lower part of face. it is worse around the injection site on the left arm . she took a benadryl last night but it did not help so i told her to go to MD. pt said she already contacted her Dr and the dr told her to go tell the pharmacist and then go to an urgent care. pt said she has no hives and no shortness of breath or trouble breathing .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: sertraline, magnesium tablets
Allergien: citrus
Vorherige Impfungen: -

VAERS 2535127

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MI
Alter: 64,0
Geschlecht: M
Eingang: 16.12.2022
Impfdatum: 12.12.2022
Beginn: 15.12.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / RA

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

Facial pain Headache Pain in jaw Trigeminal neuralgia

Symptomtext

Patient had Tdap and Covid booster on 12/12/22. He noted facial pain, jaw pain and headache starting 12/15/22. I suspect trigeminal neuralgia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: anxiety, depression, asthma, GERD, hypertension, hearing loss, meningitis, RA
Andere Medikamente: Valium-prilosec-Norvasc-wellbutrin-hygroten-hydrodiuril-cozaar-singulair-paxil-belsomra-flexeril-tumeric-deltasone-folic acid-plaquenil-methotrexate-multivitamin
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2533437

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CT
Alter: 80,0
Geschlecht: M
Eingang: 15.12.2022
Impfdatum: 09.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Anaemia Chills Cough Gait disturbance Hyperhidrosis Pyrexia

Symptomtext

Patient began to experience heavy sweats and fevers for almost 10 days following the vaccination. For the next 3 weeks, patient reports chills, intermittent fevers, cough, general weakness and an unsteady gait. Patient is also newly anemic.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: unknown at this time
Aktuelle Erkrankungen: no known
Vorgeschichte: hypertension
Andere Medikamente: -
Allergien: No known drug allergies.
Vorherige Impfungen: -

VAERS 2531002

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MI
Alter: 38,0
Geschlecht: F
Eingang: 14.12.2022
Impfdatum: 01.11.2022
Beginn: 02.11.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Injection site induration Injection site pain Laboratory test normal Lipase increased Nausea Pain Pancreatitis acute Ultrasound abdomen abnormal Vomiting

Symptomtext

Acute pancreatitis severe pain nausea vomiting elevated lipase visited ER on 11/2/22 received 2litera fluids no infection sent home

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site induration
Hospital-Tage: -
Labordaten: Lipase 11/2/22 233 Lipase 11/4/22. 42. All other lab work normal 11/4 ultrasound showed no gallstones and no reoccurrence since acute episode Arm was also very hard and tender at injection
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines
Andere Medikamente: Omitted prn
Allergien: None
Vorherige Impfungen: -

VAERS 2528221

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: IL
Alter: 64,0
Geschlecht: M
Eingang: 09.12.2022
Impfdatum: 14.11.2022
Beginn: 15.11.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Blood test Chest X-ray Computerised tomogram Confusional state Diarrhoea Disorientation Feeling abnormal Gait inability Musculoskeletal disorder Nausea Skull X-ray

Symptomtext

It seemed to have greatly amplified the adverse effects of Cipro, resulting in extreme brain fog, confusion, disorientation, nausea, uncontrolable diarrhea, and I could not walk because my legs were not working. EMS had to wheel me out of my house. I was hospitalized for four days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 4,0
Labordaten: CT scan, multiple blood tests blood tests, head and chest x-ray on 11/16/22. Blood tests several times a day 11/19/2022.
Aktuelle Erkrankungen: Ciprofloxacin was giving me brain fog, fatigue, weak legs, and mucussy diarehia.
Vorgeschichte: A-Fib. High blood pressure, under control with medication. Occasional high creatine level.
Andere Medikamente: Ciprofloxacin 500 mg Doxycycline Hyclate 100 mg Digoxin 0.25mg buPROPion 300 mg Diltiazem 180 mg Allorpurinol 300mg Atorvastatin 10mg Eliquis 5mg Iron 65mg D3 50mg C 500 MG
Allergien: -
Vorherige Impfungen: mild flu the next day. I was 63. Date was in 2021

VAERS 2528220

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: WA
Alter: 47,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 19.11.2022
Beginn: 20.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: SYR / RA

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

Contusion Injection site erythema Menstrual disorder Oligomenorrhoea Pain in extremity Peripheral swelling Skin reaction Skin warm

Symptomtext

The day of and the following morning I had sever pain in my right arm. I also had a large red bump that was hot to the touch. It turned into a bruise that lasted for 12 days. In addition my mensural cycle was 16 day late, and once my mensuration began it lasted 9 days. This is not normal for my cycles at all. I took pictures of the site of the injection with the redness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: fibromyalgia
Andere Medikamente: lisinopril, gabapentin, tylenol
Allergien: lactose
Vorherige Impfungen: -

VAERS 2527059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: IL
Alter: 50,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 26.10.2022
Beginn: 21.11.2022
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Laboratory test Nausea Vertigo

Symptomtext

I woke up and felt dizzy and nauseated. I went to the doctor and was diagnosed with vertigo. I am not going to physical therapy every day and have a check up soon. My doctor prescribed me DRAMAMINE 3 times per day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: 12/05/2022, Vertigo, unknown test
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Vitamin D complex; vitamin D; prenatal vitamin; estriol; progesterone
Allergien: Penicillin; pollen; cephalosporins
Vorherige Impfungen: -

VAERS 2526588

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: IN
Alter: 58,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 05.12.2022
Beginn: 05.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Chills

Symptomtext

Severe chills

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Calcium, VitaminD and Biotin
Allergien: None
Vorherige Impfungen: -

VAERS 2525430

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CO
Alter: 80,0
Geschlecht: F
Eingang: 07.12.2022
Impfdatum: 03.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Diarrhoea Injection site rash Nausea Rash Vomiting

Symptomtext

nausea, vomiting, diarrhea, and developed rash to L shoulder on11/4/22. the following week developed rash to face and chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: chronic back pain osteoporosis MGUS celiac disease hypertension recurrent UTI
Andere Medikamente: Current Outpatient Medications: ? alendronate (FOSAMAX) 70 mg tablet, Take 1 tablet (70 mg total) by mouth every 7 (seven) days. Take in the morning with a full glass of water, on an empty stomach, and do not take anything else by mouth o
Allergien: Allergies Alpha 1 Blocker- Quinazolines Anaphylaxis High Reaction Type: AllergyNoted: 12/26/2016 Flowers Hives, Other (see comments) High Noted: 6/25/2015 Choking Choking Gluten Other (see comments), Unknown High Reaction Type: AllergyNoted: 4/7/2015 Claimed by pt Claimed by pt Claimed by pt Mold Other (see comments) High Noted: 6/25/2015 Other Anaphylaxis High Noted: 12/26/2016 Oxycodone Unknown High Noted: 7/14/2015 Oxycodone-acetaminophen Nausea Only High Noted: 3/26/2019 Pollen Extracts Shortness of breath High Noted: 3/21/2019 Allergic to pollens and molds Allergic to pollens and molds Quinine Anaphylaxis, Rash High Reaction Type: AllergyNoted: 6/25/2015 Pt states she had a blood disease after taking quinine Pt states she had a blood disease after taking quinine Pt states she had a blood disease after taking quinine Sulfa (Sulfonamide Antibiotics) Hives, Rash High Reaction Type: AllergyNoted: 4/7/2015 Tramadol Hives, Other (see comments) High Reaction Type: AllergyNoted: 12/26/2016 Polyneuropathy in right foot Polyneuropathy in right foot Ketorolac Other (see comments) Not Specified Reaction Type: AllergyNoted: 1/13/2022 Mold Extracts Other (see comments) Not Specified Noted: 4/7/2015 Penicillins Other (see comments) Not Specified Reaction Type: AllergyNoted: 7/28/2015 Diclofenac
Vorherige Impfungen: -

VAERS 2524867

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

mild

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 01.12.2022
Beginn: 02.12.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Injection site erythema

Symptomtext

redness developed around the injection area with the size of 3 inch diameter. it got worse as days went on. patient visited ER to get the prescription for antibiotic

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: not known
Aktuelle Erkrankungen: not known
Vorgeschichte: hypertension, high cholesterol
Andere Medikamente: pfizer bivalent vaccine
Allergien: sulfa
Vorherige Impfungen: -

VAERS 2524499

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge Gj3275

mild

Staat: CA
Alter: 51,0
Geschlecht: M
Eingang: 06.12.2022
Impfdatum: 05.12.2022
Beginn: 05.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Headache Nasopharyngitis Oropharyngeal pain Pain

Symptomtext

Pain cold headache sore throat

Weitere VAERSDATA-Felder

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

VAERS 2524242

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: ID
Alter: 45,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 29.11.2022
Beginn: 02.12.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

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

Pruritus Urticaria

Symptomtext

I noticed in the evening I started to be very itchy, and I could tell I was getting hives. This is the same reaction I have whenever I come in contact with amoxicillin. I took a BENADRYL and an ALVINO bath to calm the itching. Saturday morning, I woke up and went to urgent care. They said it was hives I was given a steroid shot which helped along with PEPCID. I was also given a prescription and that night I felt them coming back. I took the PEPCID, prednisone, and ALLEGRA and I have been fine since.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: LEXAPRO
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2524156

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 07.11.2022
Beginn: 07.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Cough Dysphonia Headache Lymphadenopathy Myalgia Nasal congestion Oropharyngeal pain Pain Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test negative Swelling face

Symptomtext

Right after vaccine I started getting a headache; coughing with nasal congestion; body aches; muscle aches; swollen glands and lymph nodes and a sore throat. Two weeks later I had a change in symptoms; major congestion; puffy face; lingering cough, hoarseness. I was prescribed amoxicillin which I have been taking for 6 days. However I still have nasal mucus; chest congestion and hoarseness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: 11/30/2022 COVID-19 negative
Aktuelle Erkrankungen: Tendinitis in chest and shoulders
Vorgeschichte: Asthma; non epileptic seizures; degenerative disc disease; generalized anxiety; depression
Andere Medikamente: Fluticasone; CLARITIN; venlafaxine; baclofen; gabapentin; TOPAMAX; KLONOPIN
Allergien: None
Vorherige Impfungen: -

VAERS 2524119

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CO
Alter: 68,0
Geschlecht: M
Eingang: 06.12.2022
Impfdatum: 23.10.2022
Beginn: 26.11.2022
Tage bis Beginn: 34,0
Dosis: 5
Route/Site: SYR / RA

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

COVID-19 Fatigue Headache Nasal congestion Pyrexia SARS-CoV-2 test positive Throat irritation

Symptomtext

I received my COVID-19 5th dose on 10/23/2022. My adverse event started on 11/26/2022 in the morning around 8:00AM. I had a scratchy throat, nasal congestions, headaches, fatigue and low grade fever. On 12/05/2022 I called my doctor and she prescribed me PAXLOVID for 5-6 days. I am also taking over the counter medications such as ibuprofen and cough syrup as per needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 06DEC2022 COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Simvastatin; aspirin
Allergien: None
Vorherige Impfungen: -

VAERS 2523765

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: LA
Alter: 55,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 27.11.2022
Beginn: 27.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / RA

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

Nausea Pain Poor quality sleep Pyrexia

Symptomtext

fever; body aches; nausea; restless sleep; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 55-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 27Nov2022 at 12:30 as dose 4 (booster), single (Lot number: GJ3275) at the age of 55 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "Depression" (unspecified if ongoing). Concomitant medication(s) included: VENLAFAXINE; OSTEO BI-FLEX [ASCORBIC ACID;BOSWELLIA SERRATA RESIN;CHONDROITIN SULFATE;COLLAGEN;GLUCOSAMINE HYDROCHLORIDE;HYALURONIC ACID;MANGANESE SULFATE;METHYLSULFONYLMETHANE;SODIUM;SODIUM BORATE]; CALCIUM; CETIRIZINE. Vaccination history included: BNT162b2 (DOSE 1, SINGLE; Lot number: ER9231; Anatomical location: Left arm), administration date: 06Jan2021, when the patient was 54-year-old, for Covid-19 immunization; BNT162b2 (DOSE 2, SINGLE; Lot number: EL9261; Anatomical location: Left arm), administration date: 27Jan2021, when the patient was 54-year-old, for Covid-19 immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE; Lot Number: 330258D; Anatomical location: Left arm), administration date: 26Dec2021, when the patient was 55-year-old, for COVID-19 Immunization; flucelvax pfs (Anatomical location: Arm Left), administration date: 05Nov2022, when the patient was 55-year-old, for Immunization. The following information was reported: NAUSEA (non-serious) with onset 27Nov2022 at 22:00, outcome "recovered" (Nov2022); POOR QUALITY SLEEP (non-serious) with onset 27Nov2022 at 22:00, outcome "recovered" (Nov2022), described as "restless sleep"; PAIN (non-serious) with onset 28Nov2022 at 08:00, outcome "recovered" (Nov2022), described as "body aches"; PYREXIA (non-serious) with onset 28Nov2022 at 08:00, outcome "recovered" (Nov2022), described as "fever". Therapeutic measures were taken as a result of nausea, poor quality sleep, pyrexia, pain. Additional information: Began with nausea at 10 pm that night, restless sleep with continued nausea, by 8 am fever and body aches. Slept all day took Advil and Zofran, less nausea by 5p, still with a fever and aching. All symptoms improved and resolved by 8 am the next morning. The patient had no known allergies. The patient received other vaccines within four weeks prior to COVID vaccine. Prior to vaccination, the patient was not diagnosed with COVID-19. 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.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201346629 Same reporter/drug, different event/patient.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression
Andere Medikamente: VENLAFAXINE; OSTEO BI-FLEX [ASCORBIC ACID;BOSWELLIA SERRATA RESIN;CHONDROITIN SULFATE;COLLAGEN;GLUCOSAMINE HYDROC; CALCIUM; CETIRIZINE
Allergien: -
Vorherige Impfungen: -

VAERS 2523721

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: -
Alter: 29,0
Geschlecht: M
Eingang: 05.12.2022
Impfdatum: 30.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Rash Urticaria

Symptomtext

Patient reported hives/rash following reaction.

Weitere VAERSDATA-Felder

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

VAERS 2522919

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: VA
Alter: 47,0
Geschlecht: F
Eingang: 05.12.2022
Impfdatum: 21.10.2022
Beginn: 30.11.2022
Tage bis Beginn: 40,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 Fatigue Influenza virus test Nasal congestion Oropharyngeal pain Pain Paranasal sinus hypersecretion Pyrexia SARS-CoV-2 test SARS-CoV-2 test positive Sinus disorder

Symptomtext

I noticed body aches, fatigue and fever of 99.2. The symptoms were generally mild. Today is the 1st day without all of the symptoms. I went to urgent care on December 1st, and was swabbed for strep; COVID-19, and flu. They advised me to do over the counter medications and did not prescribe any medication. The fever has finally gone away. I am still a little stuffy and have a sore throat with sinus drainage. I do have sinus issues developing and I am unsure whether they are related

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 PCR December 1st, 2022. Flu, December 1st, 2022. COVID-19 antigen, positive December 1st, 2022. COVID-19 PCR test 12/04/2022 results unknown.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Cogan's Dystrophy; Psoriasis
Andere Medikamente: JUNEL FE; magnesium; coQ10; B12; B2; fish oil; probiotic; vitamin E; turmeric; vitamin D
Allergien: Cephalosporin
Vorherige Impfungen: -

VAERS 2522597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: GA
Alter: 69,0
Geschlecht: M
Eingang: 04.12.2022
Impfdatum: 03.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Injection site pain

Symptomtext

Site: Pain at Injection Site-Severe

Weitere VAERSDATA-Felder

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

VAERS 2522571

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: WA
Alter: 60,0
Geschlecht: M
Eingang: 03.12.2022
Impfdatum: 28.11.2022
Beginn: 28.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain upper Constipation Vertigo

Symptomtext

Patient said he was constipated the day after. Vertigo Started on 12/3/2022 and patient has left quadrant abdominal pain since approximately 12/1/2022. He has not gone to the doctor at this point. His constipation has resolved, but still having abdominal pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: blood pressure on 12/3/2022 was 146/92
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 2522546

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: NM
Alter: 85,0
Geschlecht: M
Eingang: 03.12.2022
Impfdatum: 23.11.2022
Beginn: 23.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Dizziness Eye swelling Pruritus Skin exfoliation

Symptomtext

RECEIVED FLU AND BIVALENT COVID VACCINE ON 11/23/2022 AND ON SATURDAY 11/26/2022 HE STATES HE STARTED TO ITCH ON HEAD AND ARMS AND OVER TIME GOT WORSE. THIS MORNING ON 11/30/2022 THE SKIN ON HIS FACE LOOKS PEELED AND EYES ARE SWOLLEN LEFT EYE DID CLOSE UP PATIENT ALSO FEELS DIZZY. PATIENT GIVEN DECADRON 10MG AND KENALOG 40 SHOT ADMINISTERED DURING THE VISIT. BENADRYL 25MG BY MOUTH EVERY 6 HOURS FOR THE NEXT 2 DAYS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: -
Andere Medikamente: NORVASC,VITAMINB12, CARDURA,FISH OIL, POLY VITAMIN, BENICAR HCT, CIALIS, FLOMAX, VITAMIN E, DIOVAN,
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2522539

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 03.12.2022
Impfdatum: 01.12.2022
Beginn: 02.12.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: SYR / LA

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

Erythema Feeling hot Injection site pain Swelling face

Symptomtext

Face swelling. "Red" super hot cheeks. No fever. Felt fine other than extremely red face and mildly swollen cheekbone area. Overall felt hot across whole body, no fever. Injection site was sore but tolerable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Atorvastatin 10 mg
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2522484

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

mild

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 03.12.2022
Impfdatum: 03.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Injection site pain

Symptomtext

Site: Pain at Injection Site-Severe

Weitere VAERSDATA-Felder

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

VAERS 2522075

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MA
Alter: 59,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 16.11.2022
Beginn: 20.11.2022
Tage bis Beginn: 4,0
Dosis: 5
Route/Site: IM / RA

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

Immunisation reaction Urticaria

Symptomtext

Hives on both arms, streaking both top and bottom, from top of hand to below shoulder on both arms. Described as 'covid arm'

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: no test. i just sent my primary care a note that i had the first reaction in my life to a shot, and that i was taking an anti-histamine and hoping the Hives went away sooner vs later. Using Allegra for HIVES. If no relief in another week i will ask for a steroid.
Aktuelle Erkrankungen: none.
Vorgeschichte: none.
Andere Medikamente: none.
Allergien: none.
Vorherige Impfungen: -

VAERS 2518032

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: AZ
Alter: 68,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 21.10.2022
Beginn: 25.11.2022
Tage bis Beginn: 35,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 Cough Pain SARS-CoV-2 test positive

Symptomtext

I was experiencing some symptoms on 11/23/2022 and 11/24/2022. I woke up with body aches on the morning of 11/25/2022 and tested positive with a home COVID-19 test. I placed a call with my family physician and was prescribed and received two doses of Paxlovid on 11/25/2022. I also had a horrible cough and was given Benzoate cough pearls but did not have to use my rescue inhaler. I was also taking two extra strength Tylenol in the morning and evening and am still doing that. I was instructed to stop taking Pravastatin while taking Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis; Hypertension; Asthma
Andere Medikamente: Gabapentin; Lisinopril; Arava; Duloxetine; Montelukast; Pantoprazole; Pravastatin; Levothyroxine; Xyzal; Flonase;
Allergien: Compazine
Vorherige Impfungen: -

VAERS 2517950

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: WI
Alter: 15,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 28.11.2022
Beginn: 28.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / RA

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

Dizziness

Symptomtext

After vaccination patient reported dizziness while waiting in the waiting area. Patient laid on bench and had some water. After 10 - 15 minutes she felt better and left the pharmacy with her parents.

Weitere VAERSDATA-Felder

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

VAERS 2517863

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MA
Alter: 62,0
Geschlecht: M
Eingang: 28.11.2022
Impfdatum: 16.10.2022
Beginn: 17.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Bacterial test positive Cellulitis Cyst rupture Cystitis bacterial Fatigue Impaired work ability Induration Inflammation Localised infection Pain in extremity Peripheral swelling Pilonidal disease Streptococcal infection Streptococcus test positive Ultrasound Doppler

Symptomtext

2nd day felt terrible. 3rd day had sudden eruption of a Pilonidal Cyst and simultaneously bad pain in lower right leg which eventually turned a couple of days later into Cellulitis . I was put on Bactrim and Amoxicillin . After the bacteria in the Cyst was tested and the report came back, I was switched to 20 days of Doxycycline. The infection in my right lower leg was an angry raised like 4-5 inch bubble with a raised center section-a hard ridge. Slowly over many days the leg infection cleared up slowly. My right foot became swollen and remains so even now through the ankle and toes and most of the foot. . I have never had swelling in my foot before. The left foot looks different than the right. 2 of the 5 doctors I saw told me that most likely my immune system had a strong reaction to the vaccine which caused a viral like inflammatory response both in my lower back and in the right leg which then became infected. I was out of work for a few weeks. I was so tired I could not work. I am mostly concerned now with why my foot remains swollen. The infections are gone, however you can still see a darker area where the infection on my leg predominated. I felt it important to report this course of what happened.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Testing of type of bacteria in cyst- doctor supposed that the same type of bacteria must be in the lower leg- staph and strep found. Ultrasound of right leg looking for blood clots.
Aktuelle Erkrankungen: None
Vorgeschichte: Obesity
Andere Medikamente: None
Allergien: One antibiotic. Uncooked fruit.
Vorherige Impfungen: -

VAERS 2517374

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

mild

Staat: NY
Alter: 64,0
Geschlecht: F
Eingang: 26.11.2022
Impfdatum: 14.11.2022
Beginn: 16.11.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / LA

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

Lymph node pain Lymphadenopathy

Symptomtext

Swelling and discomfort of lymph node in neck on left side (same side as vaccine administration) starting 2 days after dose. Patient chose to monitor at home and not seek medical attention. Has gradually reduced and as of 11/24/22 was almost back to baseline.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2515354

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: TX
Alter: 75,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 01.11.2022
Beginn: 20.11.2022
Tage bis Beginn: 19,0
Dosis: 6
Route/Site: IM / LA

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

COVID-19 Cough Pain Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

Congestion, runny nose, cough, fever, aches. Home test for Covid 19 positive on 11/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None.
Vorgeschichte: Diabetes; Hypertension; Neuropathy.
Andere Medikamente: Xarelto; Metformin; Amlodipine; Atorvastatin; Levothyroxine; Vitamin B; Vitamin D; Losartan; Iron; Tylenol.
Allergien: Penicillin; Bactrim.
Vorherige Impfungen: -

VAERS 2513931

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: NC
Alter: 52,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 22.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Burning sensation Rash erythematous Rash pruritic Skin warm

Symptomtext

Within 15 minutes of injections, the patient broke out in a hot, burning/itchy red rash all over her upper body. It spread down both arms and I could see it spreading up her chest and neck. We administered 25 mg oral Benadryl along with a glass of water, and after another 15 minutes the rash was subsiding to a tolerable level. When she left I instructed her to keep Benadryl with her in case she needed another dose, and to not repeat Pfizer covid vaccinations in the future. (She reported no issues with previous Pfizer or flu shots.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash erythematous
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none known
Vorgeschichte: asthma
Andere Medikamente: unknown
Allergien: tetracycline and erythromycin
Vorherige Impfungen: -

VAERS 2513892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MI
Alter: 68,0
Geschlecht: M
Eingang: 22.11.2022
Impfdatum: 27.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Injection site pain Shoulder injury related to vaccine administration X-ray limb

Symptomtext

both shoulders hurting, right much more than left. suspect Vaccine induced shoulder injury

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: pending. xray and referrral
Aktuelle Erkrankungen: -
Vorgeschichte: osteoarthritis, GERD, HTN,
Andere Medikamente: Lipitor, losartan, viagra, nexium, multivitamin, Vit D
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2513196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: OR
Alter: 69,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 05.11.2022
Beginn: 13.11.2022
Tage bis Beginn: 8,0
Dosis: 5
Route/Site: IM / LA

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

Headache Pain in jaw Paranasal sinus discomfort Paranasal sinus hypersecretion Sinus pain Sinusitis Toothache

Symptomtext

Headache, onset evening of 11/05/2022, and daily after vaccination, with increased sinus pressure and pain over sinuses, including right temple and to teeth and jaw, with clear nasal drainage, on approx. 11/12/2022. on a.m. of 11/13/2022, oral temperature 99.6F. Initiated "e-visit" for care (virtual visit.) Assessed by MD for SINUS PAIN and SINUSITIS. Treatment: Doxycycline Monohydrate 100mg oral tabs, 1 q12 hours for SINUSITIS, started on 11/13/2022, completed 11/18/2022. Also, OTC Afrin nasal decongestant (one day) and acetaminophen 500mg oral tabs prn. As of 11/20 and 11/21/2022, temperature normal. Facial sinus pain and clear drainage continues as of 11/21/2022, somewhat improved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: 10/29/2022, approx. onset, sinus pain/drainage, ?allergies
Vorgeschichte: GERD; Osteoporosis; Hypothyroidism; Rosacea; allergic rhinitis; GYN: pelvic pain; urinary bladder pain; stress incontinence
Andere Medikamente: Pantoprazole 40mg 1 twice daily; Sucralfate oral suspension 100mg/ml: 10ml bid; Alendronate 70mg once weekly; levothyroxine 75mcg one daily; Calcium carbonate 1500mg daily; Vitamin D3 1000 units daily po; estradiol 10mg vaginal tablets inse
Allergien: Penicillin; ciprofloxacin; cephalexin
Vorherige Impfungen: -

VAERS 2513059

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: CA
Alter: 31,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 14.11.2022
Beginn: 19.11.2022
Tage bis Beginn: 5,0
Dosis: 5
Route/Site: IM / -

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

Abdominal pain Abdominal pain lower Appendicectomy Appendicitis Blood test Computerised tomogram abdomen abnormal Laparoscopic surgery Nausea Urine analysis Vomiting White blood cell count

Symptomtext

Appendicitis. At 11am Sunday nausea and vomiting starting with sharp pain in lower abdomen that would come and go. At about 530pm cramping like pain began throughout the whole abdomen and by 830 was mostly on the lower right abdomen continuing to get worse. Arrived at the ER just before 930pm. Hospital was very busy so it took a long time for tests. Pain meds: dilauded, saline fluids, and zofran were given between 10-1030pm. Blood work and urine tests performed. CT scan performed. Around 1230am I was informed that inflamed appendix was confirmed, morphine was given around this time. Around 130am I met the surgeon, he ordered antibiotics and more dilauded. I was put in a room around 4am and given diapause?s every 2 hours until surgery (saline fluids continued and were constant through whole treatment). Another round of IV antibiotics were given around 11am. Surgery prep began around 1230pm, surgery performed around 130pm and I was back in my room around 2pm. I was discharged at 530pm with a prescription for Percocet. The surgery performed was a laparoscopic appendectomy. Appendix was confirmed to be inflamed and at risk of rupture (but had not yet ruptured) and the surgery was necessary.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: 2,0
Labordaten: All tests were performed Saturday 11/19 between 930 and Sunday 11/20 2am. Blood tests, specifically white blood cell count, urine tests to rule out UTI. CT scan confirmed inflamed appendix.
Aktuelle Erkrankungen: Had a cold virus that ended the week before
Vorgeschichte: Asthma PCOS Endometriosis Interstitial Cystitis
Andere Medikamente: Phentermine Elderberry and multivitamin supplements
Allergien: None
Vorherige Impfungen: -

VAERS 2512934

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

mild

Staat: WA
Alter: 81,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 03.11.2022
Beginn: 06.11.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Rash

Symptomtext

rash on arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: pacemaker, high blood pressire
Andere Medikamente: levothyroxine, ursodiol, carvedilol, amlodepine, atorvasttain, losartan, warfarin, fish oil, magnesium, calcium, cetrum, miralax
Allergien: cuedrill
Vorherige Impfungen: -

VAERS 2512378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CA
Alter: 69,0
Geschlecht: M
Eingang: 19.11.2022
Impfdatum: 17.11.2022
Beginn: 18.11.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Back pain Cough Decreased appetite Fatigue Headache Nasal congestion Pain in extremity Rhinorrhoea Upper-airway cough syndrome

Symptomtext

Headache, runny/stuffed nose, some coughing (post-nasal drip?); back and leg ache; tired (but not sleepy); lack of appetite. Ibuprofen 400mg helps with the pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Slight sinus blockage
Vorgeschichte: Gout, Vitamin B12 deficiency, bicuspid aortic valve.
Andere Medikamente: Vitamin B12 5000mg (prescribed by doctor); allopurinol 200mg
Allergien: -
Vorherige Impfungen: Fatigue, muscle aches (from COVID booster)

VAERS 2510343

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: CA
Alter: 59,0
Geschlecht: M
Eingang: 17.11.2022
Impfdatum: 11.11.2022
Beginn: 13.11.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: - / LA

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

Coordination abnormal Dizziness Feeling abnormal Feeling drunk Gait disturbance Vertigo

Symptomtext

Head was spinning light headed within one hour; Head was spinning light headed within one hour; Then as I drove home altitude 5300 foot elevation I was drunk without the alcohole; stumbling; coordination was way off, impaired; I had brain fog; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 59-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 11Nov2022 at 15:15 as dose 4 (booster), single (Lot number: GJ3275) at the age of 59 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Heart deviated septum," (unspecified if ongoing). There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Primary immunization series completed but manufacturer unknown), for Covid-19 Immunization; Bnt162b2 (DOSE 3, SINGLE; Lot number: Fh8028; Anatomical location: left arm), for Covid-19 Immunization. The following information was reported: VERTIGO (non-serious), DIZZINESS (non-serious) all with onset 13Nov2022 at 16:00, outcome "recovered" (Nov2022) and all described as "Head was spinning light headed within one hour"; FEELING ABNORMAL (non-serious) with onset 13Nov2022 at 16:00, outcome "recovered" (Nov2022), described as "I had brain fog"; FEELING DRUNK (non-serious) with onset 13Nov2022 at 16:00, outcome "recovered" (Nov2022), described as "Then as I drove home altitude 5300 foot elevation I was drunk without the alcohole"; COORDINATION ABNORMAL (non-serious) with onset 13Nov2022 at 16:00, outcome "recovered" (Nov2022), described as "coordination was way off, impaired"; GAIT DISTURBANCE (non-serious) with onset 13Nov2022 at 16:00, outcome "recovered" (Nov2022), described as "stumbling". Therapeutic measures were not taken as a result of vertigo, dizziness, feeling drunk, gait disturbance, coordination abnormal, feeling abnormal. Additional information: Head was spinning light headed within one hour. Then as he drove home altitude 5300 foot elevation he was drunk without the alcohol stumbling coordination was way off, impaired and he had brain fog. Nothing made sense of his symptoms from the vaccine. No made sense of his symptoms from the vaccine. No other symptoms, lasted 24 hours. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. The patient did not receive other vaccines within 4 weeks prior to the vaccination. The patient did not receive other medications within 2 weeks. The patient's known allergies were reported as none. AEs did not result in physician office visit or emergency room visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Ventricular septal defect
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2510337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge Gj3275

mild

Staat: WA
Alter: 39,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 28.10.2022
Beginn: 28.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / LA

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

Pruritus Rash pustular Wrong product administered

Symptomtext

Developed raised itchy raised red pustule lesions 3-4 new lesions per day. Went to doctor to be seen because the lesions hurt deeply into the tissue.; Developed raised itchy raised red pustule lesions 3-4 new lesions per day. Went to doctor to be seen because the lesions hurt deeply into the tissue.; Dose Number: 1 (Bivalent); This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 39-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Oct2022 at 10:45 as dose 1, single (Lot number: Gj3275) at the age of 39 years, in left arm for covid-19 immunization. The patient didn't receive BNT162b2 (BNT162B2). The patient's relevant medical history included: "known allergies: Sulfa" (unspecified if ongoing); "known allergies: latex" (unspecified if ongoing); "COVID" (unspecified if ongoing), notes: if covid prior vaccination: Yes. There were no concomitant medications. Vaccination history included: Flu vaccine, for Immunization, reaction(s): "known allergies: flu vaccine". The following information was reported: WRONG PRODUCT ADMINISTERED (non-serious) with onset 28Oct2022 at 10:45, outcome "unknown", described as "Dose Number: 1 (Bivalent)"; RASH PUSTULAR (medically significant), PRURITUS (medically significant) all with onset 06Nov2022 at 16:00, outcome "recovering" and all described as "Developed raised itchy raised red pustule lesions 3-4 new lesions per day. Went to doctor to be seen because the lesions hurt deeply into the tissue.". The event "developed raised itchy raised red pustule lesions 3-4 new lesions per day. went to doctor to be seen because the lesions hurt deeply into the tissue." required physician office visit and emergency room visit. Therapeutic measures were taken as a result of rash pustular, pruritus. Clinical course: Additional information: If other vaccine in four weeks: No. Other medication in two weeks: No. Facility type vaccine was Workplace clinic. No other vaccine in four weeks and other medication in two weeks. covid tested post vaccination: Unknown. Treatment provided was Acyclovir. Developed raised itchy raised red pustule lesions 3-4 new lesions per day. Went to doctor to be seen because the lesions hurt deeply into the tissue. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.; Sender's Comments: Based on the information available a possible contributory role of the suspect BNT162b2 cannot be excluded for the reported events.-WRONG PRODUCT ADMINISTERED ,RASH PUSTULAR ,PRURITUS 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: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: COVID-19 (if covid prior vaccination: Yes); Latex allergy; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2509752

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: IN
Alter: 39,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 11.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Feeling abnormal Inflammation Rash Rash erythematous Rash macular

Symptomtext

Red, inflamed spots and blotches on arms. Worsening inflammation of spider bites on neck/ upper chest area. Sensation of being in a "fog" mentally.

Weitere VAERSDATA-Felder

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

VAERS 2509667

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

mild

Staat: MO
Alter: 65,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 16.11.2022
Beginn: 16.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Dizziness Gait inability

Symptomtext

pt was dizzy, too weak to walk, she has not had any breakfast before receiving the vaccine; we provided muffins, water and eventually called paramedics to check pt's vital making sure she is ok before she go home; pt's vitals are normal and went home without going to ER;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: chronic stage 4 kidney disease
Vorgeschichte: chronic stage 4 kidney disease
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2509192

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: WI
Alter: 66,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 26.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / -

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

Asthenia Bacterial test Blood test Computerised tomogram Depression Dizziness Fall Gait disturbance Laboratory test

Symptomtext

Depression; Body weakness; Dizziness; Falling; Could hardly walk; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team, Program ID. A 66-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 26Oct2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 66 years, in arm for covid-19 immunisation. The patient's relevant medical history included: "Thyroid issues" (unspecified if ongoing), notes: Thyroid issues; "Defibrillator/pacemaker insertion" (unspecified if ongoing); "Muscular dystrophy" (unspecified if ongoing); "Parkinson's" (unspecified if ongoing), notes: Parkinson's. Concomitant medication(s) included: ALPRAZOLAM; CLONAZEPAM. Vaccination history included: BNT162b2 (First Dose: Lot EN6199), administration date: 05Mar2021, when the patient was 65-year-old, for COVID-19 immunization, reaction(s): "Severe depression", "Her body is weak in the leg, arms, hands to the point she can barely walk", "Her body is weak in the leg, arms, hands to the point she can barely walk", "Falling several times", "Dizziness", "Weakness"; BNT162b2 (Second Dose: Lot ER8733), administration date: 26Mar2021, when the patient was 65-year-old, for COVID-19 immunization, reaction(s): "Severe depression", "Her body is weak in the leg, arms, hands to the point she can barely walk", "Her body is weak in the leg, arms, hands to the point she can barely walk", "Falling several times", "Dizziness", "Weakness"; BNT162b2 (Third Dose: Lot is either 33030BD or 33030DD.), administration date: 03Dec2021, when the patient was 65-year-old, for COVID-19 immunization, reaction(s): "Severe depression", "Her body is weak in the leg, arms, hands to the point she can barely walk", "Her body is weak in the leg, arms, hands to the point she can barely walk", "Falling several times", "Dizziness", "Weakness"; BNT162b2 (Fourth Dose: Lot is either FM7553 or FM7533), administration date: 25May2022, when the patient was 66-year-old, for COVID-19 immunization, reaction(s): "Severe depression", "Her body is weak in the leg, arms, hands to the point she can barely walk", "Dizziness"; BNT162b2 (Fourth Dose: Lot is either FM7553 or FM7533), administration date: 25May2022, when the patient was 65-year-old, for COVID-19 immunization, reaction(s): "Her body is weak in the leg, arms, hands to the point she can barely walk", "Falling several times", "Weakness". The following information was reported: ASTHENIA (non-serious) with onset 2022, outcome "not recovered", described as "Body weakness"; GAIT DISTURBANCE (non-serious) with onset 2022, outcome "not recovered", described as "Could hardly walk"; DEPRESSION (non-serious) with onset 2022, outcome "not recovered"; DIZZINESS (non-serious) with onset 2022, outcome "not recovered"; FALL (non-serious) with onset 2022, outcome "not recovered", described as "Falling". Relevant laboratory tests and procedures are available in the appropriate section. Additional Information: Daughter which is the caregiver for her mom wanted to know if the onset of depression, body weakness, dizziness and falling were related to the vaccine. Reporter then stated being interested in knowing if there was anything to do to reverse the side effects and how long the vaccine stays in the system. Ever since patient has gotten it (the vaccines) or actually every time she has gotten each dose, she experiences severe depression, her body is weak in the leg, arms, hands to the point she can barely walk and was falling several times. She also experiences dizziness each time, between the dizziness and weakness she has fallen a few times because of it. Reporter was wondering if there was anything she can do to reverse the side effects or help. Reporter states that her mom has had 5 doses of the covid vaccine and all of them are Pfizer. Fifth Dose Bivalent Vaccine was on 26Oct2022 Lot was either GJ3275 or 6J3275. She received it in the Upper Arm she does not know if it was the right or left arm. The reporter clarified that only the Fifth dose was the Pfizer Covid Bivalent Vaccine. The Fifth dose was the worst for her as of side effects. Doses One to Four were the Monovalent Covid Vaccine. Reporter also clarified that each time with each dose, with the last dose being the worst, but each time her mom would experience Depression, Body weakness, and dizziness. During the call, caller's mom said she thought she had muscular dystrophy or something like that. The dizziness was on and off, it was not constant. The side effects happen with each vaccination, however the start of the side effects typically started a few days after getting the vaccine and gets worse. Investigation: She recently had a brain scan clarifying it was actually a CT scan of the brain, back and neck. She also had labs done since she is suppose to be having her hip replaced next Friday. The CT scans results had nothing, when it came back, besides showing that she has some deterioration in the hips. For the labs, she recalls is was Blood work and they did a bacterial swab, she cant remember what bacteria she was positive for but she had an infection, The CT scans and lab work was back in Sep2022 she is guessing since the doctor appointment was in early Oct2022. The patient had no allergies. Reporter states that her mom asked the doctor if she had muscular dystrophy, the doctor ruled that out, the doctor also said Parkinson's is ruled out, He ruled out all of that and said its not what it is, they don't know what it was, but just noticed it comes on every time she gets the covid vaccines. Furthermore, it was reported that Since patient started the vaccine, she overcome with depression, dizziness, and severe weakness in her arms and legs. She have fallen many times due to the weakness and dizziness. She received her last dose of the Pfizer vaccine on Wednesday 26Oct. The next day her depression was out of control and she could hardly walk. She came to realize it was the vaccine causing her problems.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201296552 Same patient, different dose and event.;US-PFIZER INC-202201296553 Same patient, different dose and event.;US-PFIZER INC-202201296554 Same patient, different dose and event.;US-PFIZER INC-202201296551 Same patient, different dose and event.;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Test Date: 202209; Test Name: Bacterial Swab; Result Unstructured Data: Test Result:Infection; Comments: she cant remember what bacteria she was positive for but she had an infection; Test Name: Blood Work; Result Unstructured Data: Test Result:Unknown result; Test Name: CT Scan Hip; Result Unstructured Data: Test Result:she has some deterioration in the hips.; Test Name: CT scan of the brain, back and neck; Result Unstructured Data: Test Result:Unknown results; Test Date: 202209; Test Name: CT scan of the brain, back and neck; Result Unstructured Data: Test Result:Unknown results; Test Name: Lab work; Result Unstructured Data: Test Result:Unknown Result; Comments: She also had labs
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Defibrillator/pacemaker insertion; Muscular dystrophy; Parkinson's disease (Parkinson's); Thyroid disorder (Thyroid issues)
Andere Medikamente: ALPRAZOLAM; CLONAZEPAM
Allergien: -
Vorherige Impfungen: -

VAERS 2507170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: WI
Alter: 72,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 14.11.2022
Beginn: 14.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Injection site rash Rash Rash erythematous Rash pruritic

Symptomtext

Patient had a rash that appeared four days after the bivalent Pfizer vaccine. The rash was bright red in color, extremely itchy, and appeared in patches. The rash was symmetrical on both arms, and extended from the top of her shoulder down to each elbow. Rash is still present one week later.

Weitere VAERSDATA-Felder

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

VAERS 2505825

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: WI
Alter: 64,0
Geschlecht: F
Eingang: 11.11.2022
Impfdatum: 03.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / LA

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

Axillary pain Ear pain Hypoacusis Pyrexia Tinnitus

Symptomtext

Day following vaccination had low-grade fever the last 2 days. Patient is most concerned with left ear pain, tinnitus, subjective difficulty hearing, axilla pain that occurred 3 days after and resolved within 1 week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: subjective axilla pain, same side as injection ear pain, tinnitus, decreased hearing--all resolved within 1 week.
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2504463

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: VA
Alter: 44,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 03.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Aphonia Dysphonia Facial pain Feeling abnormal Headache Insomnia Menstrual disorder Nasal congestion Pain Pyrexia Rhinalgia SARS-CoV-2 test Sinusitis Toothache

Symptomtext

The evening I received my vaccine, I started to feel achy, but it wasn't bad. The next day I woke up feeling ok but as the day went on, I started to feel worse. That afternoon, my fever got up to 101. That night I was unable to sleep from feeling so badly. I think I only slept 2 hours. I took over the counter medication to bring the fever down, but the fever continued to the next day. Saturday, I lost my voice completely. I continued to feel run down and had a headache through until Monday. I also felt stuffy but couldn't blow my nose. I did notice that I started my menstral cycle two weeks early. By Tuesday, my voice was returning but my teeth, nose, and face were hurting, and I could tell I was developing a sinus infection. I went to see my doctor who confirmed my concern of a sinus infection and prescribed antibiotics. At this point my voice is returning but still sounds strange. I'm also still in a lot of pain from my sinus infection in my face, head, teeth, and ears.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial pain
Hospital-Tage: -
Labordaten: 09NOV2022- COVID-19 Test- Results Unknown
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Tryptophan; Ascorbic Acid
Allergien: None
Vorherige Impfungen: -

VAERS 2504380

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CA
Alter: 82,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 01.11.2022
Beginn: 01.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Arthralgia Dysstasia Fall Gait inability Imaging procedure Laboratory test normal Loss of control of legs Muscular weakness Pain in extremity

Symptomtext

2 days after reciving her seasonal influenza and bivalent booster she started with pain in her right arm side she got the COVID shot and which progressed to leg pain and weakness bilaterally in the thighs. Patient was seen in the ED on Sunday given pain medications and was sent home. On Monday she saw her primary Dr. and talked about the pain in her arm and thighs and he felt that it was possibly an immune reaction. Later in that day as she was walking in her house her legs "buckled" and she fell down. Today she was in the bathroom and had a hard time arising from the toilet due to weakness in her lower extremities. Patient moved to a chair after this to rest and when she tried to get up she fell again. She is complaining of severe pain in her knees and lower extremities with inability to walk well as she is unsure when her legs will give out again. She denies any fever chills body aches. No nausea vomiting or diarrhea. No palpitations or chest pain prior to her falling. She denies any shortness of breath or focal weakness. Today when she fell she fell with her left leg trapped beneath her causing pain in that leg where she has had a replacement. Patient is denied any dizziness associated with all of her falls.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Patient was evaluated with laboratory and imaging 11/9/2022. She was to be discharged home as there were no acute findings. However, she feels unsafe to return home and is concerned about the increasing pain in her lower extremities. Hospitalist service was contacted to admit patient to the hospital.
Aktuelle Erkrankungen: 2 and half weeks ago patient fell and fractured the left orbit. She saw ear nose and throat and no surgery for repair is anticipated.
Vorgeschichte: PMHx of Graves' disease now hypothyroid, hypertension, osteoarthritis
Andere Medikamente: -
Allergien: NKA
Vorherige Impfungen: -

VAERS 2503878

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: NY
Alter: -
Geschlecht: M
Eingang: 10.11.2022
Impfdatum: 31.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: - / RA

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

Discomfort Inappropriate schedule of product administration Muscle strain Muscle tightness Neck pain Off label use Product use issue Swelling

Symptomtext

Right side of Neck Area soreness & pain & Pulling & Muscle Tightness up & down to Arm; Right side of Neck Area soreness & pain & Pulling & Muscle Tightness up & down to Arm; Right side of Neck Area soreness & pain & Pulling & Muscle Tightness up & down to Arm; Lots of Swelling & Discomfort on bottom of Right Armpit; Lots of Swelling & Discomfort on bottom of Right Armpit; Dose Number 1 :28Dec2021,Dose Number 2:31Oct2022; Dose Number 1 :28Dec2021,Dose Number 2:31Oct2022; Location of injection for vaccine received same date: Fluarix Quad; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 31Oct2022 at 14:00 as dose 2 (bivalent), single (Lot number: GJ3275), in right arm for covid-19 immunisation; influenza vaccine inact split 4v (FLUARIX QUADRIVALENT), on 31Oct2022 as dose number unknown, single (Lot number: 58160-0890-52), in left arm for immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose Number: 1, Batch/Lot No: 330368D, Location of injection: Arm Right, Vaccine Administration Time: 11:45 AM), administration date: 28Dec2021, for COVID-19 Immunization. The following information was reported: OFF LABEL USE (non-serious), INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (non-serious) all with onset 31Oct2022, outcome "unknown" and all described as "Dose Number 1 :28Dec2021,Dose Number 2:31Oct2022"; PRODUCT USE ISSUE (non-serious) with onset 31Oct2022, outcome "unknown", described as "Location of injection for vaccine received same date: Fluarix Quad"; SWELLING (non-serious), DISCOMFORT (non-serious) all with onset 01Nov2022, outcome "unknown" and all described as "Lots of Swelling & Discomfort on bottom of Right Armpit"; NECK PAIN (non-serious), MUSCLE STRAIN (non-serious), MUSCLE TIGHTNESS (non-serious) all with onset 01Nov2022, outcome "unknown" and all described as "Right side of Neck Area soreness & pain & Pulling & Muscle Tightness up & down to Arm". The events "right side of neck area soreness & pain & pulling & muscle tightness up & down to arm" and "lots of swelling & discomfort on bottom of right armpit" required emergency room visit. It was unknown if therapeutic measures were taken as a result of neck pain, muscle strain, muscle tightness, swelling, discomfort.

Weitere VAERSDATA-Felder

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

VAERS 2499990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: NY
Alter: 48,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 04.11.2022
Beginn: 05.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: - / RA

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

Chills Headache Myalgia Pyrexia

Symptomtext

muscle pains; Fever; chills; headache; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 48-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 04Nov2022 at 11:30 as dose 4 (booster), single (Lot number: GJ3275) at the age of 48 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "hypothyroid" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "osteoporosis" (unspecified if ongoing). Concomitant medication(s) included: FLUCELVAX QUADRIVALENT taken for immunisation, start date: 25Oct2022, stop date: 25Oct2022; RALOXIFENE; LEXAPRO; LEVOTHYROXINE; ATENOLOL; WELL [BUPROPION HYDROCHLORIDE]. Vaccination history included: BNT162b2 (DOSE 3 (BOOSTER), SINGLE; lot number: 330308D, anatomical location: right arm, , ), administration date: 29Nov2021, when the patient was 47-year-old, for COVID-19 immunization; Covid-19 vaccine (DOSE: 2; MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (DOSE: 1; MANUFACTURER UNKNOWN), for COVID-19 Immunization. The following information was reported: PYREXIA (non-serious) with onset 05Nov2022 at 03:45, outcome "recovering", described as "Fever"; CHILLS (non-serious) with onset 05Nov2022 at 03:45, outcome "recovering"; HEADACHE (non-serious) with onset 05Nov2022 at 03:45, outcome "recovering"; MYALGIA (non-serious) with onset 05Nov2022 at 03:45, outcome "recovering", described as "muscle pains". Therapeutic measures were not taken as a result of myalgia, pyrexia, chills, headache. Additional information: The patient had no known allergies. Patient didn't experience COVID prior vaccination. The patient was not tested for COVID post vaccination. The AEs did not result in physician office visit or emergency room visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension; Hypothyroidism; Osteoporosis
Andere Medikamente: RALOXIFENE; LEXAPRO; LEVOTHYROXINE; ATENOLOL; WELL [BUPROPION HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2499990

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: NY
Alter: 48,0
Geschlecht: F
Eingang: 09.11.2022
Impfdatum: 04.11.2022
Beginn: 05.11.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Chills Headache Myalgia Pyrexia

Symptomtext

muscle pains; Fever; chills; headache; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 48-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 04Nov2022 at 11:30 as dose 4 (booster), single (Lot number: GJ3275) at the age of 48 years, in right arm for covid-19 immunisation. The patient's relevant medical history included: "hypothyroid" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "osteoporosis" (unspecified if ongoing). Concomitant medication(s) included: FLUCELVAX QUADRIVALENT taken for immunisation, start date: 25Oct2022, stop date: 25Oct2022; RALOXIFENE; LEXAPRO; LEVOTHYROXINE; ATENOLOL; WELL [BUPROPION HYDROCHLORIDE]. Vaccination history included: BNT162b2 (DOSE 3 (BOOSTER), SINGLE; lot number: 330308D, anatomical location: right arm, , ), administration date: 29Nov2021, when the patient was 47-year-old, for COVID-19 immunization; Covid-19 vaccine (DOSE: 2; MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (DOSE: 1; MANUFACTURER UNKNOWN), for COVID-19 Immunization. The following information was reported: PYREXIA (non-serious) with onset 05Nov2022 at 03:45, outcome "recovering", described as "Fever"; CHILLS (non-serious) with onset 05Nov2022 at 03:45, outcome "recovering"; HEADACHE (non-serious) with onset 05Nov2022 at 03:45, outcome "recovering"; MYALGIA (non-serious) with onset 05Nov2022 at 03:45, outcome "recovering", described as "muscle pains". Therapeutic measures were not taken as a result of myalgia, pyrexia, chills, headache. Additional information: The patient had no known allergies. Patient didn't experience COVID prior vaccination. The patient was not tested for COVID post vaccination. The AEs did not result in physician office visit or emergency room visit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypertension; Hypothyroidism; Osteoporosis
Andere Medikamente: RALOXIFENE; LEXAPRO; LEVOTHYROXINE; ATENOLOL; WELL [BUPROPION HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2507046

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: -
Alter: 45,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 31.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Myalgia

Symptomtext

Myalgia & Arthralgia Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2502576

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: TX
Alter: 71,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

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

Injection site erythema Injection site mass Injection site warmth SARS-CoV-2 test negative Ultrasound scan normal

Symptomtext

11/04/2022 09:30PM after I got out of the shower, I noticed I had a soft ball size lump on the right leg. It was red, and hot. It was where the vein doctor gave me the injection at for a problem I was having. I knew what she will say so decided to go to the ER. At the ER they did ultrasound and every was normal. I had a follow up with my vein doctor today 11/08/2022 at 09:45AM to check for the procedure that was done 2 weeks ago. The vein doctor said that the medication that is used in the anti-inflammatory drug that she used in the injection was also used in the vaccine which caused it to flare up where the procedure was done.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: 08NOV2022 COVID-19 test negative
Aktuelle Erkrankungen: Nose
Vorgeschichte: POTS; Neuro cardiogenic Syncope; Mitral Valve Prolapse; Intersectoral Cystitis; GERD; Migraines
Andere Medikamente: Fludrocortisone; propranolol; rosuvastatin; estradiol; meclizine; vitamin D3; calcium; TYLENOL ARTHRITIS; FLONASE
Allergien: CIPRO; VENTOLIN; amrinone; CELEBREX; sugar alcohol; triarimol
Vorherige Impfungen: -

VAERS 2500715

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 21.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: - / LA

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

Cough Fatigue Hepatomegaly Malaise Myalgia Pain in extremity Pyrexia Respiratory tract congestion Splenomegaly

Symptomtext

Sore arm, fever, muscle ache, congestion, cough, extreme fatigue, swollen spleen and liver. It felt like my Epstein Barr Virus was activated felt like I had mono all over again was sick for 2 weeks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, Factor IV
Andere Medikamente: Cozar, Trazadone, spirolactone
Allergien: None
Vorherige Impfungen: -

VAERS 2499322

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: UT
Alter: 56,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 02.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

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

Chest discomfort Rash

Symptomtext

Patient broke out in rash all over body after complaining of chest tightness the day before. Patient will be visiting doctor

Weitere VAERSDATA-Felder

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

VAERS 2499229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 28.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Arthralgia Fatigue Lymphadenopathy

Symptomtext

enlarged lymph nodes left arm, back of neck and groin, extreme joint pain, fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: htn,cva
Andere Medikamente: valsartan /hctz, amlodipine, crestor, tylenol, vitamin d
Allergien: none
Vorherige Impfungen: -

VAERS 2499160

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MN
Alter: 55,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 28.10.2022
Beginn: 30.10.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / LA

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

Abdominal pain upper Injection site pain Loss of personal independence in daily activities Lymphadenopathy Muscle contractions involuntary Muscle spasms

Symptomtext

I woke around 06:00 in the morning to severe pain in my stomach, my deltoid muscle where I received I injection, my trapezoid muscles. My lymph nodes on both sides are swollen but the left side are so swollen, I am unable to do anything. I went to the doctor and was given pain medication and muscle relaxer, so I am able to be to be comfortable and sleep. I have tried icing the muscles this only irritates the muscles. Heat does not help either. When the contractions from the muscle spasms happen, I am rendered helpless.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Migraines
Andere Medikamente: Buspirone; Wellbutrin SR; Prilosec DR; Vitamin D3; Vitamin K2; Biotin
Allergien: Morphine; Dairy sensitivity; Wheat sensitivity
Vorherige Impfungen: -

VAERS 2497811

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: FL
Alter: 43,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 28.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Eye pain Headache Muscle tightness

Symptomtext

Onset of Headache 4 days after injection. Headache continuous for 48 hours, then subsided for about 8 hours, reoccurred overnight and is continuing. Attempted treatment of acetaminophen every 6 hours but nothing is working to stop it. Headache is contained to to left side and behind left eye, some tension in neck and shoulder on that side. Currently day 6 post injection with no relief.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: None yet
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Mounjaro 2.5 mg/weekly Alprazolam .5 mg as needed Ondansetron 4 mg as needed Magnesium Glycinate 400 mg daily B12 injections weekly
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2497263

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / RA

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

Arthralgia Asthenia Back pain Hypoaesthesia Interchange of vaccine products Pain Pain in extremity

Symptomtext

Whole body is sore; I have body ache all over, including my wrist, my knuckles, my hands, my arms, the back of my legs; I have body ache all over, including my wrist, my knuckles, my hands, my arms, the back of my legs; I have body ache all over; my lower back, upper back; Feels like an intense workout that won't go away. Can't lift her baby; Numb to right arm and hand/Numb to right arm and hand; Interchange of vaccine products; 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 38-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 24Oct2022 at 16:30 as dose 4 (booster), single (Lot number: GJ3275) at the age of 38 years, in right arm for covid-19 immunisation; influenza vaccine (FLU VACCINE VII), on 18Oct2022 as dose number unknown, single (Batch/Lot number: unknown), in left arm for immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: moderna vaccine (Dose 3 (Booster), Single, Manufacturer: Moderna, Date: 24Nov2021, LOT: 066F21A, NDC/EXPIRY/Formulation/Dose: Unknown), administration date: 24Nov2021, when the patient was 37-year-old, for Covid-19 immunization, reaction(s): "No reaction"; moderna vaccine (Dose 2, Single, Manufacturer: Moderna, Date: 17May2021, LOT: 026C21A, NDC/EXPIRY/Formulation/Dose: Unknown), administration date: 17May2021, when the patient was 37-year-old, for Covid-19 immunization, reaction(s): "No reaction"; moderna vaccine (Dose 1, Single , Manufacturer: Moderna, Date: 19Apr2021, LOT: 038B21A, NDC/EXPIRY/Formulation/Dose: Unknown), administration date: 19Apr2021, when the patient was 37-year-old, for Covid-19 immunization, reaction(s): "No reaction"; Flu vaccine (Received flu vaccines the last 5 to 8 years, once a year), for immunisation. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 24Oct2022, outcome "unknown"; ASTHENIA (non-serious) with onset 26Oct2022, outcome "unknown", described as "Feels like an intense workout that won't go away. Can't lift her baby"; ARTHRALGIA (non-serious), PAIN IN EXTREMITY (non-serious) all with onset 26Oct2022, outcome "unknown" and all described as "I have body ache all over, including my wrist, my knuckles, my hands, my arms, the back of my legs"; BACK PAIN (non-serious) with onset 26Oct2022, outcome "unknown", described as "I have body ache all over; my lower back, upper back"; HYPOAESTHESIA (non-serious) with onset 26Oct2022, outcome "not recovered", described as "Numb to right arm and hand/Numb to right arm and hand"; PAIN (non-serious) with onset 26Oct2022, outcome "not recovered", described as "Whole body is sore". Therapeutic measures were taken as a result of pain, arthralgia, pain in extremity, back pain, asthenia, hypoaesthesia, interchange of vaccine products. Additional information: Consumer stated that she thinks she had adverse reaction to the Pfizer booster. So, she was getting, she had body ache all over, including her wrist, knuckles, hands, arms, the back of legs, lower back, upper back. NDC number, Expiry Date and UPC number of Covid Vaccine Booster was Unknown. She got the vaccine on Monday which she thought if she had the body ache, it will be Monday and tuesday but she did not feel anything until Wednesday in the AM. And she was still having reactions from it. She wanted to know if this was a common side effect. Consumer was informed about the role of Pfizer Drug Safety and Pfizer Medical Information department and telephone was shared as (phone number withheld), option 3, 8 AM to 9 PM, Monday to Friday, as per EST. Product details, Pharmacy details and other details could not be probed as consumer was unwilling to complete the report. Hence further probing could not be done. Limited information available over the call. Upon follow-up 31Oct2022, updated Reporter 1 salutation. Patient Ethnicity updated. Vaccination date and Lot number updated. Caller wanted to know if the Pfizer BionTech Covid-19 Bivalent Vaccine (was unable to specify if orange or gray) has an effect to breastfeeding. As per DSU agent, caller got her Pfizer BionTech Covid-19 Bivalent Vaccine (was unable to specify if orange or gray) last Monday 24Oct2022. She said that the lot number was GJ3275 while DSU agent was endorsing the call. Age was 38 Years Old. Gender was Female. She received a booster dose with a Pfizer Biontech COVID 19 vaccine (no formulation was specified by the caller). She received the booster last Monday at did not have any side effects until 2-3 days later. She mentioned her whole body was sore, and it has been sore since Wednesday, for 5 days already. Caller asked if this might be a delayed side effect to the vaccine. She also stated that all of her previous vaccines have been from Moderna, with no reaction to any of them. This was her second booster dose. Caller also asked how long do the side effects last. Whole body was sore from Around midnight 26Oct2022 and Ongoing. Numb to right arm and hand from 26Oct2022 and Ongoing. No other conditions, Investigations and other products. Reporting a side effect to Pfizer COVID-19 Vaccine Booster dose. Transfer agent not able to confirm if the Booster dose was Pfizer COVID-19 Vaccine Bivalent or not, caller just said Pfizer's. The caller clarified the information provided by the transfer agent. Took the Pfizer COVID-19 Vaccine Booster on Monday, 24Oct2022, and didn't feel it until Wednesday, 26Oct2022, in the morning. It was a delayed reaction. Patient Height was about 5 feet 2 inches tall and weight about probably about 95 pounds. Doesn't feel like it worsened. Today was first day she was feeling better. Only place not sore was her feet. Feels like an intense workout that won't go away. Can't lift her baby. Took flu shot recently. May have been given on 18Oct2022. Specific product name, manufacturer, NDC/LOT/EXPIRY/Formulation/Dose was Unknown. Concerned because she was breastfeeding and hopes it doesn't effect anything, requested transfer back to Pfizer Medical Information for guidance. Pfizer/BioNtech COVID-19 Vaccine 1st dose at 4:30pm and Anatomical Site of injection: Right Arm. Injection, not sure just a needle to arm to muscle. Does get numb in that arm and that hand. Numb to right arm and hand. Vaccination Facility Type was Hospital. Prior Vaccinations (within 4 weeks) was Flu Vaccine. Route, Anatomical Location was Left Arm Muscle. No. of Previous Doses and Dates was for this year just that one. Received flu vaccines the last 5 to 8 years, once a year. Patient medical history (including any illness at time of vaccination), Family Medical History Relevant to Adverse Events (AEs), Relevant Tests was None. Surgical procedures and dates were None. The event does not require the initiation of new medication/other treatment/ procedure. Her doctor recommend she take 650mg but doesn't have time to grab that medicine. Aware this was discrepant as caller previously provided, she has to take Tylenol to function. Product clarified from Pfizer COVID-19 Vaccine Booster to Pfizer Bivalent COVID-19 Vaccine. Aware this was discrepant as caller previously provided and referred to product as Pfizer COVID-19 Vaccine Booster multiple times in the call. Updated suspect product as clarified by caller. Caller provided LOT: GJ3275. Seriousness Criteria that caller provided was moderate to severe. AE does not require visit to ER or physician office. Have to take Tylenol to function to get through the day. Tylenol Dose: 500mg per tablet and takes two tablets, Expiry was May2025.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Breast feeding
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2497150

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: IA
Alter: -
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Body temperature Chills Glossodynia Headache Joint noise Lymphadenopathy Nausea Pain Pseudolymphoma Pyrexia

Symptomtext

Nausea; Aches and pains; Severe headache; Chills; I had a fever of about a 100.3; Started developing submandibular lymph node swelling; Developed sores on my tongue; Joint sounds like weird but some kinds of weird lumps over my joints appeared; weird lumps over my joints appeared like my knee joint like a lymphoma almost like lymphoma; This is a spontaneous report received from a contactable reporter(s) (Nurse), Program ID. The reporter is the patient. A 56-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), as dose number unknown (booster), single (Lot number: GJ3275) for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing), notes: Nurse stated, as just when it needed, I haven't taken anything for Asthma for probably a month now; "Hypothyroidism" (unspecified if ongoing); "PSVT " (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE taken for hypothyroidism; PROPRANOLOL taken for supraventricular tachycardia. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for COVID-19 Immunization. The following information was reported: NAUSEA (non-serious), outcome "unknown"; PAIN (non-serious), outcome "unknown", described as "Aches and pains"; HEADACHE (non-serious), outcome "unknown", described as "Severe headache"; CHILLS (non-serious), outcome "unknown"; PYREXIA (non-serious), outcome "unknown", described as "I had a fever of about a 100.3"; LYMPHADENOPATHY (non-serious), outcome "recovered", described as "Started developing submandibular lymph node swelling"; GLOSSODYNIA (non-serious), outcome "recovered", described as "Developed sores on my tongue"; JOINT NOISE (non-serious), outcome "unknown", described as "Joint sounds like weird but some kinds of weird lumps over my joints appeared"; PSEUDOLYMPHOMA (non-serious), outcome "recovering", described as "weird lumps over my joints appeared like my knee joint like a lymphoma almost like lymphoma". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of nausea, pain. Additional information: About asthma medication, nurse stated, "as just when it needed, she hasn't taken anything for Asthma form probably a month now. No Investigations performed. Nurse (patient), on the line. She called to report side effect that were unusual. The she was in hurry. When probed for the concern, transferring agent stated, "She was reported side effect that are unusual once after having the Pfizer Bivalent Vaccine (Pfizer COVID-19 Bivalent Vaccine). She got a month ago, COVID shot (Pfizer COVID-19 Bivalent Vaccine) and also to give the COVID shots that's her job. Not have pharmacy email address. Vaccine expiration date, NDC# and UPC#, Nurse stated, No. Any laboratory test, Nurse stated, Not since February and everything was, all her lab work was normal. Any treatment for the event, Nurse stated, "Yes, she received a Zofran for the severe nausea and Ibuprofen for aches and pains, Zofran was Ondansetron, as these two words for it but the Zofran was the easiest one to tell and then Ibuprofen. Nurse stated, so, started within 6 hours she had severe headache, nausea and that's normal. Chills, she had a fever of about a 100.3, this was 5 days before she had it on the 23rd and then had started next day developed a what her husband said submandibular lymph node swelling and she had also developed sores on her tongue but they have went away and also like joint it sounds like weird but some kinds of weird lumps over her joints appeared like her knee joint like a lymphoma almost like lymphoma but it wasn't and it went away within about a day and then one the lump came back now and all that went away. Causality: Nurse stated, " she does, and her husband also a doctor and they both think that it was of the Vaccine. Relatedness of drug to reaction(s)/event(s): Source of assessment: Primary Source Reporter; Method of assessment: Global Introspection; Result of Assessment: Yes with all the events. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: Test Name: Body temperature; Result Unstructured Data: Test Result:100.3; Comments: I had a fever of about a 100.3
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma (Nurse stated, as just when it needed, I haven't taken anything for Asthma for probably a month now); Hypothyroidism; Paroxysmal supraventricular tachycardia
Andere Medikamente: LEVOTHYROXINE; PROPRANOLOL
Allergien: -
Vorherige Impfungen: -

VAERS 2495057

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 28.10.2022
Beginn: 01.10.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: IM / LA

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

Injection site rash Injection site swelling Lymphadenopathy

Symptomtext

" I got a bump and rash on my left arm at the site of the injection on Friday. I also had a swollen lymph node on my left underarm."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2495009

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: FL
Alter: 66,0
Geschlecht: M
Eingang: 01.11.2022
Impfdatum: 26.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Dizziness postural

Symptomtext

DIZZINESS WHEN STANDING UP, HAVE TO HOLD ON WHEN GETTING UP

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness postural
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: HYPERTENION, HYPERLIPIDEMIA,
Andere Medikamente: -
Allergien: NO ALLERGIES
Vorherige Impfungen: -

VAERS 2494012

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MI
Alter: 55,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 24.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 2,0
Dosis: 4
Route/Site: IM / RA

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

Injection site pain Injection site pruritus Pruritus Rash

Symptomtext

1 day after vaccine itch and pain at injection site, two days visible bumps on upper body (Arm Chest and back), Third day bumps on entire body, itching intense. Husband went to pharmacy, asked pharmacist what i should do, advised Benadryl. I took Benadryl, but did not help, with itching.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: none, doctors appt. Thursday November 4
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, High Blood Pressure
Andere Medikamente: Tresiba Insulin, Novolog Insulin, Atenolol, Xanax
Allergien: -
Vorherige Impfungen: -

VAERS 2493888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 31.10.2022
Impfdatum: 01.10.2022
Beginn: 01.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Lymph node pain Rash

Symptomtext

Rash on administered arm, sore lymph node on underarm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: N/A
Vorgeschichte: -
Andere Medikamente: Clobetasol
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2493732

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 29.10.2022
Impfdatum: 26.10.2022
Beginn: 25.10.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Chills Headache Myalgia

Symptomtext

Headache, Myalgia, chills Narrative:

Weitere VAERSDATA-Felder

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

VAERS 2492681

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 25.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Injection site pain Screaming Wrong technique in product usage process

Symptomtext

PATIENT STATED THAT AFTER SHE ARRANGED HER SHIRT SLEEVE FOR THE SHOT, SHE WAS GIVEN THE SHOT IMMEDIATELY WITHOUT WARNING AND IT WAS SHOT " LIKE A DART". THE PHARMACIST DID NOT WARN HER SHE WAS ABOUT TO GIVE IT, AND THE PATIENT SCREAMED . THE PATIENT STATED THAT THIS WAS THE MOST PAINFUL SHOT THAT SHE HAS EVER HAD AND THAT THE PHARMACIST DID NOT HOLD HER ARM TO ADMINISTER THE SHOT AND WAS NOT GENTLE. PATIENT STATES THAT EVEN AT 10 PM THAT NIGHT SHE HAD TO TAKE MELOXICAM FOR THE PAIN

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: UNKNOWN
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 2492279

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

mild

Staat: OH
Alter: 52,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 21.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / RA

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

Dermatitis allergic Injection site pruritus Pruritus Rash Rash pruritic

Symptomtext

Site: Itching at Injection Site-Mild, Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Systemic: rash under breasts-Mild, Additional Details: Patient received vacccine and a day later had an itchy rash under her breasts

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2492122

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: CA
Alter: 77,0
Geschlecht: U
Eingang: 28.10.2022
Impfdatum: 21.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / LA

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

Body temperature Fatigue Feeling hot Malaise Peripheral coldness Pyrexia Vaccination site erythema Vaccination site pain

Symptomtext

I have the fever; I am really tired; My arm hurts; its red right where the injection was like the size of 50 cent coin and it hurts to touch and its red; red right where the injection was like the size of 50 cent coin; All day along I have been laying down; I am cold and my hands are freezing and my feet are freezing, rest of me is warm and my face feels very warm now. I just took my temperature, its 98.6; rest of me is warm and my face feels very warm now; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 77-year-old patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 21Oct2022 as dose 3 (booster), single (Lot number: GJ3275) at the age of 77 years, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (DOSE 1, Unknown manufacturer), for COVID-19 Immunization; Covid-19 vaccine (DOSE 2, Unknown manufacturer), for COVID-19 Immunization. The following information was reported: MALAISE (non-serious) with onset 2022, outcome "unknown", described as "All day along I have been laying down"; PERIPHERAL COLDNESS (non-serious) with onset 2022, outcome "unknown", described as "I am cold and my hands are freezing and my feet are freezing, rest of me is warm and my face feels very warm now. I just took my temperature, its 98.6"; FATIGUE (non-serious) with onset 2022, outcome "unknown", described as "I am really tired"; PYREXIA (non-serious) with onset 2022, outcome "unknown", described as "I have the fever"; VACCINATION SITE PAIN (non-serious) with onset 2022, outcome "unknown", described as "My arm hurts; its red right where the injection was like the size of 50 cent coin and it hurts to touch and its red"; VACCINATION SITE ERYTHEMA (non-serious) with onset 2022, outcome "unknown", described as "red right where the injection was like the size of 50 cent coin"; FEELING HOT (non-serious) with onset 2022, outcome "unknown", described as "rest of me is warm and my face feels very warm now". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Patient got the third vaccine (clarified as Pfizer Covid-19 vaccine Bivalent) yesterday and Patient was fine but just today Patient really tired, arm hurts. Patient got the injection on the left arm and its red right where the injection was like the size of 50 cent coin and it hurts to touch and its red. Patient have the fever. All day along patient have been laying down and Patient cold and hands are freezing and feet are freezing, rest of me is warm and my face feels very warm now. Patient just took temperature, it is 98.6. And Patient just feel really tired and did not happen with other vaccines. Patient just wanted to know if this is the part of injection, fever, because Patient never get fever and Patient really have fever. Reporter stated, is there any one to talk about these side effects Is there any one to talk to or do Patient call where Patient got the injection. Patient was 5 feet and why is this important. Follow-up attempts are completed. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Date: 20221022; Test Name: Body temperature; Result Unstructured Data: Test Result:98.6; Comments: I just took my temperature, it is 98.6
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2491994

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: KS
Alter: 69,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Diarrhoea Feeling cold Hyperhidrosis Immediate post-injection reaction

Symptomtext

After pt got shots, she stated 5 minutes after got cold and sweaty then vomited and had diarrhea. She described both as severe for several minutes then she felt better. At time of reporting to us she felt fine. Had not had reactions to any other Covid or Flu vaccines. Pt is a physician and will report if has further problems.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: None at this time
Aktuelle Erkrankungen: None disclosed
Vorgeschichte: None disclosed
Andere Medikamente: Flu shot also given Pt takes Metformin
Allergien: Sulfa and Nitrofurantoin
Vorherige Impfungen: -

VAERS 2491525

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CA
Alter: 71,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 20.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: - / LA

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

Imaging procedure Lymph node pain Mastication disorder Pain in jaw

Symptomtext

Left side general jaw pain. Neck and lymph nodes. Pain when chewing on that side. Dentist confirmed not tooth issue. Pain persists 6 days after injection.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: 10/27/2022 imaging and discussion with dentist confirms not a dental issue.
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: Hydrochlorthiazide Losartan
Allergien: None
Vorherige Impfungen: -

VAERS 2493777

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge gj3275

mild

Staat: -
Alter: 42,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Fatigue Headache Myalgia Pain

Symptomtext

Headache, Myalgia, extreme fatigue, extreme body aches Narrative:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: yes-the employee has had similar reactions to the other vaccines

VAERS 2490415

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 26.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Pain in extremity

Symptomtext

Member is feeling well at this time only having sore arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: None listed
Vorherige Impfungen: -

VAERS 2490413

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: CA
Alter: 48,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 26.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

Chills Dizziness Immediate post-injection reaction

Symptomtext

Patient got Pfizer bivalent booster. She has received Pfizer for her primary series and initial booster previously. Within 5 minutes after vaccination, she felt shiver running down her vaccination arm and felt dizzy. I laid her down on her back and elevated her feet, applied cold compress on her wrist. After 5 minutes she felt better. I had her rest for another 5 minutes. And then she was able to sit up and rest for another 5 -10 minutes. Patient felt fine afterwards.

Weitere VAERSDATA-Felder

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

VAERS 2490136

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: WI
Alter: 23,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 20.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / LA

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

Asthenia Dizziness Fatigue

Symptomtext

A staff member at this assisted living facility. After receiving the vaccinations, she complained of feeling very tired/weak and like she was going to pass out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2490052

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: WI
Alter: 47,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 25.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Pruritus

Symptomtext

Within 5 minutes of receiving the vaccination, individual experienced itching throughout her body.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: 50 mg Benadryl given IM
Aktuelle Erkrankungen: NA
Vorgeschichte: NA
Andere Medikamente: NA
Allergien: NA
Vorherige Impfungen: -

VAERS 2489466

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: MN
Alter: -
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 18.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

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

Overdose Product administered to patient of inappropriate age Pyrexia

Symptomtext

fever; The reporter was under the impression that patient received covid 19 gray cap, monovalent instead of the omicron booster vaccine. pharmacy was adamant that her daughters received the correct vaccine; The reporter was under the impression that patient received covid 19 gray cap, monovalent instead of the omicron booster vaccine. pharmacy was adamant that her daughters received the correct vaccine; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. A 9-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 18Oct2022 as dose 4 (booster), single (Lot number: GJ3275) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose 1, single), for COVID-19 immunization; Covid-19 vaccine (Dose 2, single), for COVID-19 immunization; Covid-19 vaccine (Dose 3, single), for COVID-19 immunization. The following information was reported: PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious), OVERDOSE (non-serious) all with onset 18Oct2022, outcome "unknown" and all described as "The reporter was under the impression that patient received covid 19 gray cap, monovalent instead of the omicron booster vaccine. pharmacy was adamant that her daughters received the correct vaccine"; PYREXIA (non-serious), outcome "unknown", described as "fever". Additional Information: The reporter was under the impression her daughters, 9-year-old and 8-year-old daughters received covid 19 gray cap, monovalent instead of the omicron booster vaccine. She called the pharmacy, and the pharmacy was adamant that her daughters received the correct vaccine and asked what vaccine was this, based on Lot number recorded. Reporter stated that reporter's daughter received the monovalent Covid-19 vaccine as their booster dose. Patient was supposed to have been receiving the Bivalent booster dose (lot number: GJ3275). Reporter didn't think it was the new Omicron booster that her daughters received and didn't know if it was the pediatric dose or what. Her daughters were having side effects, but they had side effects with the other vaccines as well, so she's not really worried about that. But, when she found out they didn't get the right booster dose, it made her concerned. Pharmacy insisted that her daughters received the bivalent booster vaccine yesterday (18Oct2022). Reporter asked if someone can look up the lot number and tell her which vaccine that LOT was for. She trusted Pfizer over the pharmacy, so she wants to check the lot number first.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201243364 same reporter/ drug/ event for different patients;

Weitere VAERSDATA-Felder

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

VAERS 2489465

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: MN
Alter: -
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 18.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

Overdose Product administered to patient of inappropriate age Pyrexia

Symptomtext

fever; The reporter was under the impression that patient received covid 19 gray cap, monovalent instead of the omicron booster vaccine. pharmacy was adamant that her daughters received the correct vaccine; The reporter was under the impression that patient received covid 19 gray cap, monovalent instead of the omicron booster vaccine. pharmacy was adamant that her daughters received the correct vaccine; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the parent. An 8-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 18Oct2022 as dose 4 (booster), single (Lot number: GJ3275) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Dose 1, single), for COVID-19 immunization; Covid-19 vaccine (Dose 2, single), for COVID-19 immunization; Covid-19 vaccine (Dose 3, single), for Covid-19 immunization. The following information was reported: PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (non-serious), OVERDOSE (non-serious) all with onset 18Oct2022, outcome "unknown" and all described as "The reporter was under the impression that patient received covid 19 gray cap, monovalent instead of the omicron booster vaccine. pharmacy was adamant that her daughters received the correct vaccine"; PYREXIA (non-serious), outcome "unknown", described as "fever". Additional Information: The reporter was under the impression her daughters, 9-year-old and 8-year-old daughters received covid 19 gray cap, monovalent instead of the omicron booster vaccine. She called the pharmacy, and the pharmacy was adamant that her daughters received the correct vaccine and asked what vaccine was this, based on Lot number recorded. Reporter stated that reporter's daughter received the monovalent Covid-19 vaccine as their booster dose. Patient was supposed to have been receiving the Bivalent booster dose (lot number: GJ3275). Reporter didn't think it was the new Omicron booster that her daughters received and didn't know if it was the pediatric dose or what. Her daughters were having side effects, but they had side effects with the other vaccines as well, so she's not really worried about that. But, when she found out they didn't get the right booster dose, it made her concerned. Pharmacy insisted that her daughters received the bivalent booster vaccine yesterday (18Oct2022). Reporter asked if someone can look up the lot number and tell her which vaccine that LOT was for. She trusted Pfizer over the pharmacy, so she wants to check the lot number first.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201243532 same reporter/ drug/ event for different patients;

Weitere VAERSDATA-Felder

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

VAERS 2484870

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MN
Alter: 9,0
Geschlecht: F
Eingang: 26.10.2022
Impfdatum: 18.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Asthenia Fatigue Headache Nausea Product administered to patient of inappropriate age Incorrect dose administered Pyrexia Wrong product administered

Symptomtext

Daughter was given 12+ Pfizer Bivalent Shot (gray cap) when it was supposed to be pediatrics dose (orange cap)

Weitere VAERSDATA-Felder

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

VAERS 2488629

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MI
Alter: 22,0
Geschlecht: U
Eingang: 25.10.2022
Impfdatum: 21.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / LA

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

Feeling abnormal Headache Vertigo

Symptomtext

Vaccines given at appt 10/21/22, the next morning pt developed vertigo symptoms, headache and brain fog, other symptoms were mild and have since resolved, vertigo worsened throughout the day and has persisted. Brain fog will happen for 10-15 min at a time intermittently throughout the day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: morbid obesity, exertional chest pain, tonsillar hypertrophy, recurrent tonsillitis, TMJ, prediabetes, PCOS, anxiety and depression, psychophysiological insomnia, localized edema, syncope
Andere Medikamente: famotidine 40mg, orthocyclen 0.25-35mcg
Allergien: cumin, mint, PCN
Vorherige Impfungen: -

VAERS 2488261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: ND
Alter: 48,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 20.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 1,0
Dosis: 4
Route/Site: IM / RA

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

Blood pressure increased Electrocardiogram Fatigue Headache Laboratory test Malaise Oropharyngeal pain Pain

Symptomtext

I experienced body aches, sore throat. I ended getting treatment because my blood pressure elevated for one month. I went to ER due to a bad headache and blood pressure elevated. I had lab work and EKG done. I also got monitored for a heart attack. I still feel sick and feel very tired and have not recovered from my symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Lab work; EKG
Aktuelle Erkrankungen: Sinus Infection
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin, Fosamax
Vorherige Impfungen: -

VAERS 2487247

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: OH
Alter: 80,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 20.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / -

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

Back pain Chills Disturbance in attention Fatigue Gait disturbance Pyrexia

Symptomtext

Had chills about 3 hours later, a fever, very tired, on 10/21 started having lower back pain. Had a hard time walking, felt like I couldn't walk, and it took a lot of focus to get my feet to move the way I wanted them to.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Colon Cancer - survivor Stage 4 kidney disease Diabetes
Andere Medikamente: Gabapentin, allopurinol, amlodipine, aspirin, basagler, carvedilol , chlorthalidone, famotidine, iron, lisopro (as needed), lisartin, matinax, multi vitamin, vitamin C, Vitamin D, Zetia
Allergien: latex, cipro, pravastatin, sulfa
Vorherige Impfungen: -

VAERS 2487026

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

mild

Staat: OH
Alter: 40,0
Geschlecht: F
Eingang: 24.10.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Dizziness

Symptomtext

Patient stated she felt light headed @1:35pm. 1st set of vitals BP102/64, pulse 78, Oxygen sta. 98% on room air and RR 25. Pt offered water and was able to keep water down. After 0 min. pt began to feel better and her normal self. Pt states she received influenza vaccine 10/20/22, one day prior to COVID-19 Bivalent booster vaccine. Post status vitals at 1:55pm BP 11070, Pulse 55, RR 18, oxygen saturation 98% on Room Air.

Weitere VAERSDATA-Felder

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

VAERS 2484871

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: MN
Alter: 8,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 18.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / AR

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

Fatigue Headache Incorrect dose administered Product administered to patient of inappropriate age

Symptomtext

Pfizer COVID-19 Bivalent Booster 12+ dose given to child under 12. Child experienced headache and fatigue 36-48 hours after vaccination.

Weitere VAERSDATA-Felder

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

VAERS 2484036

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

mild

Staat: NY
Alter: 33,0
Geschlecht: M
Eingang: 20.10.2022
Impfdatum: 20.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Dizziness Nervousness Pallor

Symptomtext

5 min after the immunizations the patient reported to feel dizzy, faint and was visibly pale and shaky. I sat the patient down gave him Snapple to drink, called 911 and observed him until Ems came in. He had also asked for water which was provided as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: not known
Vorgeschichte: not known
Andere Medikamente: not known
Allergien: not known
Vorherige Impfungen: -

VAERS 2484026

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: TN
Alter: 65,0
Geschlecht: F
Eingang: 20.10.2022
Impfdatum: 16.10.2022
Beginn: 16.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Abnormal dreams Asthenia Chills Fatigue Headache Hypophagia Lethargy Nausea Retching Sleep disorder Vomiting

Symptomtext

Nauseousness and vomiting (dry heaves mostly and constant every 15-30 minutes) 7 PM 10/16 through 4 AM 10/19; chills on day 1; headaches, lethargic (exhausted after walking the dog....and I am a marathon runner ...very active); sleopt for first day after Monday 10/17 then could not sleep much after for daysbut also could not get up energy to get out of bed; vivid dreams or mind drifting awake or asleep (very intense); could not keep a drop of water down or food therfeore went almost 40 hours with nothing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: none
Vorgeschichte: CLL diagnosed 10/20 no treatment (wait and see)
Andere Medikamente: Atovastarin 40 mg
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2481153

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

mild

Staat: WA
Alter: 60,0
Geschlecht: F
Eingang: 17.10.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Pain Peripheral swelling Swelling

Symptomtext

Patient has had pain and swelling since the evening of vaccination. Swelling is in her armpit, front and back of arm and up to neck/collarbone area. Patient says it continues to get worse. She is trying to reach her primary care provider to have it looked at.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: had chills, fatigue at time of illness possibly due to anemia her md thought, was having bloodwork done
Vorgeschichte: type 2 diabetes, hypertension
Andere Medikamente: Cetirizine 10mg, Hydroxyurea 500mg, Amlodipine 5mg,
Allergien: tetanus vaccine
Vorherige Impfungen: teranus

VAERS 2479302

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

mild

Staat: FL
Alter: 68,0
Geschlecht: F
Eingang: 15.10.2022
Impfdatum: 10.10.2022
Beginn: 11.10.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Discomfort Fatigue Injection site erythema Injection site pain Injection site swelling Lethargy Pain Rash Sleep disorder

Symptomtext

Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Allergic: Rash Generalized-Severe, Systemic: Body Aches Generalized-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Unable to Sleep-Severe, Additional Details: unsual discomfort

Weitere VAERSDATA-Felder

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

VAERS 2728327

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: CA
Alter: 75,0
Geschlecht: F
Eingang: 28.12.2023
Impfdatum: 17.11.2022
Beginn: 07.12.2023
Tage bis Beginn: 385,0
Dosis: 5
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 symptoms started 07Dec2023 Started Paxlovid that night. Became negative 12Dec or 13Dec.; Covid symptoms started 07Dec2023 Started Paxlovid that night. Became negative 12Dec or 13Dec.; This is a spontaneous report received from a Consumer or other non HCP from product quality group. A 76-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 17Nov2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 75 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 31Jan2021 as dose 1, single (Lot number: 9265), in left arm, on 21Feb2021 as dose 2, single (Lot number: EN6200), in left arm, on 10Oct2021 as dose 3 (booster), single (Lot number: FH8020), in left arm and on 12Jun2022 as dose 4 (booster), single (Lot number: FJ4991), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Low thyroid" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing); "Allergy: Sulfa" (unspecified if ongoing); "Allergy: Iodine" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 07Dec2023, outcome "recovered" (Dec2023) and all described as "Covid symptoms started 07Dec2023 Started Paxlovid that night. Became negative 12Dec or 13Dec.". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Dec2023) negative, notes: Became negative 12Dec or 13Dec; (Dec2023) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 with Paxlovid from 07Dec2023 to 12Dec2023.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300455101 Same patient/same product, different dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 202312; Test Name: Covid test; Test Result: Negative ; Comments: Became negative 12Dec or 13Dec; Test Date: 202312; Test Name: Covid test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: High cholesterol; Iodine allergy; Sulfonamide allergy; Thyroid disorder
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2727585

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ3275

gering

Staat: AR
Alter: 76,0
Geschlecht: F
Eingang: 27.12.2023
Impfdatum: 25.10.2022
Beginn: 27.12.2023
Tage bis Beginn: 428,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19

Symptomtext

hospitalized with covid

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: Dementia , Afib , HTN , CVA/TIA, PVD, Anx , Dep, diverticulosis
Andere Medikamente: unknown
Allergien: lorazepam Allergy (Verified 12/26/23 21:28) Hallucinations morphine Allergy (Verified 12/26/23 21:28) Hallucinations Sulfa (Sulfonamide Antibiotics) Allergy (Verified 12/26/23 21:28) Allergic Reactions midazolam Adverse Reaction (Verified 12/26/23 21:28) Allergic Reactions
Vorherige Impfungen: -

VAERS 2723875

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: FL
Alter: 62,0
Geschlecht: F
Eingang: 14.12.2023
Impfdatum: 16.11.2022
Beginn: 01.07.2023
Tage bis Beginn: 227,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 16Nov2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 62 years, in left arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 30Mar2021 as dose 1, single (Lot number: ER8730), in left arm, on 20Apr2021 as dose 2, single (Lot number: ER8729), in left arm, on 08Nov2021 as dose 3 (booster), single (Lot number: FE3590), in left arm and on 26May2022 as dose 4 (booster), single (Lot number: FK9893), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Rheamatoid Arthritis" (unspecified if ongoing); "Atrial Septal Anurism" (unspecified if ongoing); "Iron Anemic" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Jul2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19 which included Paxlovid from 22Jul2023 to 24Jul2023. Clinical course: The patient also received COMIRNATY (2023-2024 Formula) on 19Oct2023 at 01:00 PM as dose 1, single in left arm for covid-19 immunisation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anemia iron deficiency; Interatrial septal aneurysm; Rheumatoid arthritis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2714812

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: PA
Alter: 56,0
Geschlecht: F
Eingang: 16.11.2023
Impfdatum: 08.11.2022
Beginn: 01.01.2023
Tage bis Beginn: 54,0
Dosis: 1
Route/Site: SYR / LA

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

Alopecia Alopecia universalis Biopsy skin abnormal Blood test normal

Symptomtext

Alopecia Universalis. Two months after receiving vaccine, patient experienced extreme hair loss on scalp. By June 2023, patient was completely bold on scalp and also has complete hair loss on entire body. Pattern of hair loos - scalp, face and arms, eye brows and lashes, legs and pubic hair.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alopecia
Hospital-Tage: -
Labordaten: March 13 blood work at normal June 22 autoimmune blood work normal June 22 referred to endocrinologist July 11 endocrinologist reported no findings in thyroid issue. Nov. 1 dermatologist did biopsy of scalp and concludes diagnosis as alopecia universalis.
Aktuelle Erkrankungen: none.
Vorgeschichte: none.
Andere Medikamente: Estrodiol, multi-vitamin, collagen.
Allergien: none
Vorherige Impfungen: -

VAERS 2700912

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MN
Alter: 24,0
Geschlecht: F
Eingang: 24.10.2023
Impfdatum: 23.01.2023
Beginn: 24.10.2023
Tage bis Beginn: 274,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Patient vaccinated against and then tested positive for COVID19

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2697511

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 59,0
Geschlecht: F
Eingang: 18.10.2023
Impfdatum: 01.11.2022
Beginn: 01.10.2023
Tage bis Beginn: 334,0
Dosis: 4
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; 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 (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 01Nov2022 as dose 4 (booster), single (Lot number: GJ3275) at the age of 59 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: "High blood pressure" (unspecified if ongoing); "thyroid" (unspecified if ongoing), notes: thyroid; "known allergies: sulpha" (unspecified if ongoing); "known allergies: Cefzin" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Oct2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19 with Paxlovid treatment from 05Oct2023 to 10Oct2023.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300329739 same patient/reporter, different drug/event (Paxlovid case);

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Drug allergy; Sulfonamide allergy; Thyroid disorder (thyroid)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2689132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 01.10.2023
Impfdatum: 13.11.2022
Beginn: 01.12.2022
Tage bis Beginn: 18,0
Dosis: UNK
Route/Site: IM / RA

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

Joint range of motion decreased Muscular weakness

Symptomtext

Patient has had gradual onset of right arm weakness and decreased range of motion

Weitere VAERSDATA-Felder

Praegender Schweregrund: Joint range of motion decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2681055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: -
Alter: 52,0
Geschlecht: F
Eingang: 11.09.2023
Impfdatum: 21.10.2022
Beginn: 01.08.2023
Tage bis Beginn: 284,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 53-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 21Oct2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 52 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), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Zoloft, reaction(s): "Known allergy: Zoloft". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Aug2023, outcome "not recovered" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical Course: Patient received Paxlovid from start 30Aug2023 to 03Sep2023 as treatment of COVID-19.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300295333 same patient, different drug/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2680603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: NY
Alter: 54,0
Geschlecht: F
Eingang: 08.09.2023
Impfdatum: 19.10.2022
Beginn: 26.08.2023
Tage bis Beginn: 311,0
Dosis: 5
Route/Site: - / -

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

COVID-19 Drug ineffective Full blood count

Symptomtext

I have had five Pfizer Vaccines for Covid and I didn't have Covid so, I got Covid recently; I have had five Pfizer Vaccines for Covid and I didn't have Covid so, I got Covid recently; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 55-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 19Oct2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 54 years for covid-19 immunisation; BNT162b2 (BNT162B2), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Diabetic" (unspecified if ongoing), notes: Diabetic. Concomitant medication(s) included: LOSARTAN POTASSIUM taken for diabetes mellitus; CENTRUM FOR WOMEN; METFORMIN HCL; ATORVASTATIN. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 26Aug2023, outcome "unknown" and all described as "I have had five Pfizer Vaccines for Covid and I didn't have Covid so, I got Covid recently". The patient underwent the following laboratory tests and procedures: Full blood count: Normal. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient finished the 5 doses and then five days after that of Paxlovid as covid-19 treatment. Patient is not taking Atorvastatin now, she haven't taken it since she got Covid. She normally takes it but was not taking it while being sick. 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: CBC blood work; Result Unstructured Data: Test Result:Normal
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diabetic
Andere Medikamente: LOSARTAN POTASSIUM; CENTRUM FOR WOMEN; METFORMIN HCL; ATORVASTATIN
Allergien: -
Vorherige Impfungen: -

VAERS 2679830

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 07.09.2023
Impfdatum: 23.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / RA

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). The reporter is the patient. A 59-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 23Nov2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 59 years, in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 30Jul2022 as dose 4 (booster), single (Lot number: FP7138), in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 27Feb2021 as dose 1, single (Lot number: EN6203), in right arm, on 20Mar2021 as dose 2, single (Lot number: ER8730), in right arm and on 11Oct2021 as dose 3 (booster), single (Lot number: FF8839), in right arm for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. 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.

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, Comment: Other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2676514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: AR
Alter: 81,0
Geschlecht: F
Eingang: 25.08.2023
Impfdatum: 03.11.2022
Beginn: 23.08.2023
Tage bis Beginn: 293,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Hospitalized with covid; fully vaccinated with 3 boosters

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 1,0
Labordaten: positive covid pcr 8/23/23
Aktuelle Erkrankungen: unknown
Vorgeschichte: Anticoagulant Therapy, Bleeding Tendencies, CAD, Hypertension, Hyperlipidemia, Stent(s) and Valve Dz/Murmur, sleep apnea
Andere Medikamente: unknown
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2657351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: -
Alter: 29,0
Geschlecht: F
Eingang: 18.07.2023
Impfdatum: 10.11.2022
Beginn: 01.07.2023
Tage bis Beginn: 233,0
Dosis: 5
Route/Site: - / -

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 30-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Nov2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 29 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), as dose 3 (booster), single (Batch/Lot number: unknown) and as dose 4 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Pituitary surgeries" (not ongoing); "hypopituitarism" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Cefepime, reaction(s): "ALLERGY TO CEFEPIME". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jul2023, outcome "recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (13Jul2023) Negative, notes: Rebound / return of symptoms after testing negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient received COVID 19 Treatment as Paxlovid with start date 05Jul2023 and stop date 10Jul2023.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300250720 same reporter/patient, different drug/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20230713; Test Name: COVID-19 testing; Test Result: Negative ; Comments: Rebound / return of symptoms after testing negative
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Endocrine gland operation; Hypopituitarism
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2655628

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: WA
Alter: -
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 10.11.2022
Beginn: 01.06.2023
Tage bis Beginn: 203,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 Interchange of vaccine products Vaccination failure

Symptomtext

Interchange of vaccine products; 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 female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Nov2022 as dose 5 (booster), single (Lot number: GJ3275), in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 09Feb2021 as dose 1, single (Batch/Lot number: unknown), in left arm and on 02Mar2021 as dose 2, single (Batch/Lot number: unknown), in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 01Dec2021 as dose 3 (booster), single (Lot number: 058H21A), in left arm and on 09Aug2022 as dose 4 (booster), single (Lot number: 055A22A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXINE, start date: 01Jun2023, stop date: 10Jul2023. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Jun2023, outcome "recovering" and all described as "COVID 19 Treatment"; INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "recovering". Therapeutic measures were taken as a result of vaccination failure, covid-19 with Paxlovid. Clinical course: Patient started taking Paxlovid on 2nd day of symptoms and positive testing. Experienced only mild symptoms while taking Paxlovid. After the 5-day treatment, she began to experience moderate symptoms for another 10 days. She was still test positive 2 weeks after starting the Paxlovid. 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-202300247506 Same Patient, different drug/events;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Hypothyroidism
Andere Medikamente: LEVOTHYROXINE
Allergien: -
Vorherige Impfungen: -

VAERS 2655420

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 12.07.2023
Impfdatum: 26.10.2022
Beginn: 13.11.2022
Tage bis Beginn: 18,0
Dosis: 4
Route/Site: IM / LA

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

Angioedema Hypersensitivity

Symptomtext

ANGIOEDEMA, INIT ALLERGIC REACTION, INIT ALLERGIC REACTION, SUBSEQ

Weitere VAERSDATA-Felder

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

VAERS 2652775

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 8,0
Geschlecht: F
Eingang: 05.07.2023
Impfdatum: 11.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / -

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

Incorrect dose administered

Symptomtext

Patient received Pfizer bivalent 12+ dose when Pfizer bivalent 5-11yo dose was indicated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2649834

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: -
Alter: 80,0
Geschlecht: M
Eingang: 27.06.2023
Impfdatum: 21.10.2022
Beginn: 27.03.2023
Tage bis Beginn: 157,0
Dosis: 5
Route/Site: IM / LA

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

Asthenia Hypothyroidism Hypoxia

Symptomtext

R09.02 HYPOXIA 3/27/2023 HYPOTHYROIDISM R09.02 HYPOXIA 3/27/2023 WEAKNESS

Weitere VAERSDATA-Felder

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

VAERS 2649022

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: -
Alter: 73,0
Geschlecht: F
Eingang: 23.06.2023
Impfdatum: 12.12.2022
Beginn: 01.02.2023
Tage bis Beginn: 51,0
Dosis: 5
Route/Site: - / -

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

Blood thyroid stimulating hormone decreased Graves' disease Thyroid stimulating immunoglobulin Thyroxine free increased Tri-iodothyronine

Symptomtext

Grave's disease

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood thyroid stimulating hormone decreased
Hospital-Tage: -
Labordaten: FT4 0.9 - 1.7 ng/dL 2.4 High 0.8 R 0.8 R Comment: (NOTE) New method and reference range effective 07/18/2022. TSH 0.270 - 4.200 uIU/mL <0.005 Low Thyroid stimulating immunoglobulin 24.8 total T3 162
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2642335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: NE
Alter: 27,0
Geschlecht: F
Eingang: 07.06.2023
Impfdatum: 06.12.2022
Beginn: 13.04.2023
Tage bis Beginn: 128,0
Dosis: 4
Route/Site: SYR / RA

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

Blood test Contusion

Symptomtext

I had bruising all over my body

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood test
Hospital-Tage: -
Labordaten: blood work
Aktuelle Erkrankungen: None
Vorgeschichte: Acid reflux, Sleep Apnea
Andere Medikamente: Mili: Claritin: Esomeprazole Magnesium
Allergien: Cinnamon, Latex
Vorherige Impfungen: -

VAERS 2641252

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: -
Alter: -
Geschlecht: F
Eingang: 06.06.2023
Impfdatum: 02.12.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / -

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

COVID-19 Drug ineffective

Symptomtext

Drug ineffective; COVID-19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. An adult female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 02Dec2022 as dose 5 (booster), single (Lot number: GJ3275) for covid-19 immunisation; BNT162b2 (BNT162B2), on 15Jul2022 as dose 4 (booster), single (Lot number: FM7553) 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. The patient's concomitant medications were not reported.The following information was reported: DRUG INEFFECTIVE (medically significant), outcome "not recovered"; COVID-19 (medically significant), outcome "not recovered". Therapeutic measures were taken as a result of drug ineffective, covid-19 (Paxlovid). No follow-up attempts are possible. No further information is expected.

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, Comment: Other medical history: No
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2640196

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: VA
Alter: 30,0
Geschlecht: F
Eingang: 02.06.2023
Impfdatum: 03.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / RA

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

Abortion spontaneous Exposure during pregnancy

Symptomtext

Event- miscarriage History- 5 weeks pregnant, previous miscarriage in May 2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abortion spontaneous
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: prenatal vitamin, vitamin D 200 units
Allergien: None
Vorherige Impfungen: -

VAERS 2639094

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 31.05.2023
Impfdatum: 14.10.2022
Beginn: 26.05.2023
Tage bis Beginn: 224,0
Dosis: 1
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 admission after one bivalent dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2637297

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

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Staat: TX
Alter: 31,0
Geschlecht: F
Eingang: 26.05.2023
Impfdatum: 21.11.2022
Beginn: 09.05.2023
Tage bis Beginn: 169,0
Dosis: 4
Route/Site: SYR / LA

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

Lichen planopilaris

Symptomtext

I was diagnosed with Frontal Fibrosting Alopecia 12MAY2023, I first noted in the summer of 2021 looking back in pictures it actally started in 2020. I did not seek medical attention until April 2023. Symtoms started before I was ever vaccinated and I have had confirmed COVID-19 January 2022 and unconfirmed in January 2020.

Weitere VAERSDATA-Felder

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

VAERS 2635694

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ3275

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Staat: NV
Alter: 49,0
Geschlecht: F
Eingang: 23.05.2023
Impfdatum: 21.05.2023
Beginn: 21.05.2023
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / LA

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

Extra dose administered

Symptomtext

Patient received 2nd dose of updated covid booster of Moderna Bivalent vaccine. Patient is 49 years old, and works with immunocompromised and is not eligible or fall under: "People aged 65 years and older may get a 2nd dose of updated Pfizer-BioNTech or Moderna COVID-19 vaccine." per CDC guidelines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: N/A
Allergien: NO KNOWN ALLERGIES
Vorherige Impfungen: -

VAERS 2635403

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge gj3275

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Staat: MA
Alter: 64,0
Geschlecht: F
Eingang: 23.05.2023
Impfdatum: 29.03.2023
Beginn: 29.03.2023
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered No adverse event

Symptomtext

no adverse event, patient was given an expired dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2634123

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

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Staat: WV
Alter: 70,0
Geschlecht: F
Eingang: 19.05.2023
Impfdatum: 13.11.2022
Beginn: 01.04.2023
Tage bis Beginn: 139,0
Dosis: 5
Route/Site: IM / RA

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

Dysphonia Goitre Pharyngitis streptococcal Streptococcus test positive

Symptomtext

I developed a sore throat, but didn't have a fever. I waited to see if a fever to see if it was strep throat but one never came in. My voice gradually became hoarse, so I decided to visit my clinic. They told me my thyroid seemed to be enlarged during examination and conducted a throat swab on me to test for viral and bacterial infections. It came back positive for strep throat, and I was prescribed me Azithromycin 500mg for 5 days for recovery. This is the second time this has happened in between vaccinations of contracting a strep throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dysphonia
Hospital-Tage: -
Labordaten: APR2023 -- Throat Swab
Aktuelle Erkrankungen: N/A
Vorgeschichte: Pacemaker; Osteoarthritis
Andere Medikamente: Metoprolol; Meloxicam; Osteo Bi-Flex; Calcium; Aspirin; Vitamin D3; Multivitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2631622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

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Staat: MI
Alter: 59,0
Geschlecht: F
Eingang: 13.05.2023
Impfdatum: 04.11.2022
Beginn: 15.01.2023
Tage bis Beginn: 72,0
Dosis: UNK
Route/Site: IM / LA

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

Vertigo

Symptomtext

I do not know if vertigo has anything to do with this vaccine and don't blame a vaccine for it. I'm only doing this report because I got a follow-up call from vaccine study. I have vertigo. It started approx 1/15/23. I went to the doctor on 2/1/23 and was given Fluticasone Propionate nose spray and Meclizine. I got better for a couple weeks and then it came back. I have it right now and will have to go back to the doctor.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vertigo
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure and prediabetes.
Andere Medikamente: Amlodapine Besylate 10mg
Allergien: none that I know of
Vorherige Impfungen: -

VAERS 2630772

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

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Staat: AZ
Alter: 47,0
Geschlecht: F
Eingang: 12.05.2023
Impfdatum: 27.12.2022
Beginn: 07.04.2023
Tage bis Beginn: 101,0
Dosis: 4
Route/Site: - / -

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

Carbohydrate antigen 125 Computerised tomogram Endometriosis Magnetic resonance imaging Ovarian cyst ruptured SARS-CoV-2 test Ultrasound scan

Symptomtext

a 6 x 10 x 6 ovarian endometrioma settled in front of bladder; Ovarian cyst ruptured; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 47-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 27Dec2022 as dose 4 (booster), single (Lot number: GJ3275) at the age of 47 years for covid-19 immunisation. The patient's relevant medical history included: "anxiety" (unspecified if ongoing); "depression" (unspecified if ongoing); "Beta-thalassemia" (unspecified if ongoing); "Covid", start date: 11Dec2020, stop date: 11Dec2020. Concomitant medication(s) included: ESCITALOPRAM; CLONAZEPAM; MUSHROOM COMPLEX [ALLIUM SATIVUM;GANODERMA LUCIDUM;HERICIUM ERINACEUS;INONOTUS OBLIQUUS;LENTINUS EDODES]. Vaccination history included: BNT162b2 (DOSE 1,SINGLE, Batch/Lot number: ER2613, Anatomical location: Left arm), administration date: 17Mar2021, for COVID-19 immunisation; BNT162b2 (DOSE 2, SINGLE, Batch/Lot number: ER8730, Anatomical location: Left arm), administration date: 07Apr2021, for COVID-19 immunisation, reaction(s): "Ovarian cyst ruptured"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Batch/Lot number 3302688), administration date: 17Nov2021, for COVID-19 immunisation. The following information was reported: OVARIAN CYST RUPTURED (medically significant) with onset 07Apr2023, outcome "unknown"; ENDOMETRIOSIS (medically significant), outcome "unknown", described as "a 6 x 10 x 6 ovarian endometrioma settled in front of bladder". The patient underwent the following laboratory tests and procedures: Carbohydrate antigen 125: (unspecified date) 120, notes: CA-125 = 120; Computerized tomogram: (unspecified date) Unknown results; Magnetic resonance imaging: (unspecified date) 6 x 10 x 6 ovarian endometrioma, notes: settled in front of bladder, location unusual, Unknown if malignant. No lymph node inflammation. No ascites; SARS-CoV-2 test: (Feb2022) Negative, notes: Nasal Swab; (Sep2022) Negative, notes: Nasal Swab; (11Dec2020) Positive, notes: Other; Ultrasound scan: (unspecified date) Unknown results. Therapeutic measures were taken as a result of ovarian cyst ruptured, endometriosis. Clinical course: Never had cysts prior. Bilat salpingo-oophorectomy w/ hysterectomy scheduled 08May2023. Tramadol Aug2021 & Apr2023. Sender's Comments: Based on the current available limited information in the case provided, the causal association between the events Ovarian cyst ruptured, Endometriosis and the use of suspect product Comirnaty cannot be fully excluded. The impact of this report on the benefit-risk profile of the Pfizer product and on the conduct of the study is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate. Linked Report(s): US-PFIZER INC-202300185334 same patient and reporter, different doses and event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Carbohydrate antigen 125
Hospital-Tage: -
Labordaten: Test Name: CA-125; Result Unstructured Data: Test Result:120; Comments: CA-125 = 120; Test Name: CT; Result Unstructured Data: Test Result: Unknown results; Test Name: MRI w/ contrast; Result Unstructured Data: Test Result:6 x 10 x 6 ovarian endometrioma; Comments: settled in front of bladder, location unusual, Unknown if malignant. No lymph node inflammation. No ascites; Test Date: 202202; Test Name: Binax NOW/SARS-CoV-2 test; Test Result: Negative; Comments: Nasal Swab; Test Date: 202209; Test Name: SARS-CoV-2 test; Test Result: Negative; Comments: Nasal Swab; Test Date: 20201211; Test Name: Rapid PCR/SARS-CoV-2 test; Test Result: Positive; Comments: Other; Test Name: transvag; Result Unstructured Data: Test Result: Unknown results.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; COVID-19; Depression; Thalassemia beta
Andere Medikamente: ESCITALOPRAM; CLONAZEPAM; MUSHROOM COMPLEX [ALLIUM SATIVUM;GANODERMA LUCIDUM;HERICIUM ERINACEUS;INONOTUS OBLIQUUS;LENTINUS EDO
Allergien: -
Vorherige Impfungen: -

VAERS 2628671

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

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Staat: AZ
Alter: 47,0
Geschlecht: F
Eingang: 08.05.2023
Impfdatum: 27.12.2022
Beginn: 07.04.2023
Tage bis Beginn: 101,0
Dosis: 1
Route/Site: IM / AR

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

Carbohydrate antigen 125 increased Computerised tomogram abnormal Endometriosis Magnetic resonance imaging abnormal Mass Ovarian cyst ruptured Scan with contrast abnormal Ultrasound scan vagina abnormal

Symptomtext

After my 1st vaccine ever administered on 17-Mar-2021, I had my first ovarian cyst rupture in August 2021. I followed up with imaging since then with my gynecologist, Dr and have had multiple cysts on my ovaries. My second cyst ruptured on April 7, 2023, about 4 months after my 2nd Pfizer booster. Please note all Pfizer vaccine dates and lot #'s have been reported through Pfizer Safety Reporting #COV-2305-Prxw9z. It was then that the ER physician discovered a mass after I had a CT scan w/ and w/o contrast. I followed up with Dr. and this was thought to be an ovarian endometrioma per transvag ultrasound. However, I was referred to a gynecologic oncologist b/c my CA-125 biomarker was elevated at Anything over 35 is above the normal range. I had an MRI w/ and w/o contrast and it showed that the ovarian endometrioma was approximately 6 x 10 x 6 cm and located unusually in front of my bladder. No lymph node inflammation noted. No ascites noted. Uterus unremarkable. I am having surgery tomorrow, 09-May-2023, to remove the endometrioma, get it biopsied, and I also need a salpingo-oophorectomy with a hysterectomy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Carbohydrate antigen 125 increased
Hospital-Tage: -
Labordaten: CT scan 07-Apr-2023, CA-125 biomarker 10-Apr-2023 (CA-125=120), Transvag U/S 11-Apr-2023, MRI w/ and w/o contrast 25-Apr-2023
Aktuelle Erkrankungen: None
Vorgeschichte: Beta-thalassemia, anxiety, depression
Andere Medikamente: Escitalopram, Clonazepam, Mushroom supplements
Allergien: None known
Vorherige Impfungen: -

VAERS 2627907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

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Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 07.05.2023
Impfdatum: 09.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Amnesia Brain fog Burning sensation Head discomfort Mental impairment

Symptomtext

Develop bilateral nerve burning sensations from shoulders to fingers. Sensations was continuous and lasted for 3 days. Brain fog also developed and is still experiencing now. Memory loss, head feels heavy, difficulty thinking and recalling events, names or objects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Amnesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2626646

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: OR
Alter: 55,0
Geschlecht: M
Eingang: 04.05.2023
Impfdatum: 18.12.2022
Beginn: 20.01.2023
Tage bis Beginn: 33,0
Dosis: 5
Route/Site: IM / AR

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

Swelling Therapeutic procedure

Symptomtext

I did not have an adverse reaction to the vaccine. I have had a problem with an enlarged prostate for 2 years. On 01/20/2023, I had the rezum procedure. I had a follow up appointment today and I was advised it will take time for the swelling to go down.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Swelling
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Finasteride
Allergien: Seasonal Allergies
Vorherige Impfungen: -

VAERS 2625747

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

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Staat: OH
Alter: 72,0
Geschlecht: F
Eingang: 03.05.2023
Impfdatum: 26.10.2022
Beginn: 01.02.2023
Tage bis Beginn: 98,0
Dosis: 5
Route/Site: IM / AR

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

Cataract operation Vertigo Visual impairment

Symptomtext

I started having trouble with my vision. I wasn't seeing things in my right eye very well at far distances. I went to the eye doctor, and they told me I didn't have Glaucoma. I had Cataract surgery a while ago and he thinks I am having issues with my Cataract lens. I had to go to a Neurologist because I am also having Vertigo. The last time I had it was 27 years ago, but it came about 7 or 8 years ago. I have an appointment with a specialist soon, but in the meantime, I am taking Meclizine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cataract operation
Hospital-Tage: -
Labordaten: FEB2023 Eye Exam - Abnormal
Aktuelle Erkrankungen: N/A
Vorgeschichte: Arthritis; Migraines; High Cholesterol
Andere Medikamente: Rizatriptan; Meclizine; Citalopram; Atorvastatin; Omega 3; Mind Works; Aspirin; Zinc; Colligan; Vitamin C; Turmeric; Glucosamine; Multivitamin; CPAP; Magnesium; Calcium; Vitamin D3; Protein
Allergien: Adhesive; Sudafed
Vorherige Impfungen: -

VAERS 2621892

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

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Staat: NY
Alter: 71,0
Geschlecht: F
Eingang: 27.04.2023
Impfdatum: 14.12.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / -

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

Tinnitus

Symptomtext

Tinnitus; This is a spontaneous report received from a contactable reporter(s) (Physician) from medical information team, Program ID: The reporter is the patient. A 71-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Dec2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 71 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot: EL9262), administration date: 23Jan2021, when the patient was 69-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE, Lot: EL9266), administration date: 13Feb2021, when the patient was 69-year-old, for COVID-19 immunization; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Lot: EW0217), administration date: 15Sep2021, when the patient was 70-year-old, for COVID-19 immunization; BNT162b2 (DOSE 4 (BOOSTER), SINGLE, Lot: FK9894), administration date: 16Apr2022, when the patient was 70-year-old, for COVID-19 immunization. The following information was reported: TINNITUS (non-serious), outcome "not recovered". The event "tinnitus" required physician office visit. Therapeutic measures were not taken as a result of tinnitus. Additional information: The patient did not receive any other vaccines within 4 weeks prior vaccination.

Weitere VAERSDATA-Felder

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

VAERS 2618493

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: VA
Alter: 60,0
Geschlecht: F
Eingang: 20.04.2023
Impfdatum: 12.01.2023
Beginn: 22.02.2023
Tage bis Beginn: 41,0
Dosis: 5
Route/Site: IM / LA

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

Cardiac flutter Cardiac stress test normal Chest discomfort Echocardiogram normal Electrocardiogram ambulatory normal Heart rate increased Laboratory test normal Middle insomnia

Symptomtext

Around 02/22/2023, I got up in the middle of the night and I had a fluttering, uncomfortable feeling in my chest. When I checked my pulse rate, it was 137 and I hadn't done anything to make it go up that high. I went to the doctor the next day. Because I have a family history of heart issues, he wanted me to go to the cardiologist. I've had a plethora of tests, but as far as I know, all of the results came back normally. I will follow up, but it hasn't happened before and hasn't happened since.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cardiac flutter
Hospital-Tage: -
Labordaten: 14MAR2023 Holter Monitor Test, nothing abnormal found; 31MAR2023 Stress Test, nothing abnormal found; 06APR2023 Ultrasound of Heart, nothing abnormal found
Aktuelle Erkrankungen: None
Vorgeschichte: Acid Reflux
Andere Medikamente: Pantoprazole; vitamin D; vitamin B12; vitamin B6; elderberry with vitamin C and zinc
Allergien: MINOCIN
Vorherige Impfungen: -

VAERS 2617163

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

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Staat: VA
Alter: 70,0
Geschlecht: F
Eingang: 19.04.2023
Impfdatum: 17.11.2022
Beginn: 11.04.2023
Tage bis Beginn: 145,0
Dosis: 6
Route/Site: - / -

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

Body height Body temperature COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

She got COVID; She got COVID; 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 70-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 17Nov2022 as dose 6 (booster), single (Lot number: GJ3275) at the age of 70 years, in arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 25Feb2021 as dose 1, single (Lot number: EN5318), in arm, on 25Mar2021 as dose 2, single (Lot number: EN6199), in arm, on 03Sep2021 as dose 3 (booster), single (Lot number: FC3182), in arm, on 17Mar2022 as dose 4 (booster), single (Lot number: FK9895), in arm and on 17Aug2022 as dose 5 (booster), single (Lot number: FP7150), in arm for covid-19 immunisation. The patient's relevant medical history included: "Rheumatoid arthritis", start date: 1983 (unspecified if ongoing); "immunocompromised" (unspecified if ongoing); "heart patient" (unspecified if ongoing); "cough" (unspecified if ongoing); "got three replacement joints" (unspecified if ongoing); "surgery" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 11Apr2023, outcome "unknown" and all described as "She got COVID". The patient underwent the following laboratory tests and procedures: Body height: (unspecified date) 4ft 11in, notes: Lost a couple of inches stating 4ft 11in is probably correct; Body temperature: (unspecified date) 100, notes: she got a low grade fever of 100-100.1; (unspecified date) 100.1, notes: she got a low grade fever of 100-100.1; SARS-CoV-2 test: (unspecified date) Negative, notes: Tested negative after a couple days; (11Apr2023) Positive, notes: She was positive for COVID again on 11Apr2023. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Symptoms started evening of 10Apr2023. First day she could go out with the mask on was 10Apr2023 and she felt a little bit of symptoms that night. She was positive for COVID again on 11Apr2023.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300157613 Same product and event, different patient;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Body height
Hospital-Tage: -
Labordaten: Test Name: Height; Result Unstructured Data: Test Result:4ft 11in; Comments: Lost a couple of inches stating 4ft 11in is probably correct; Test Name: fever; Result Unstructured Data: Test Result:100; Comments: she got a low grade fever of 100-100.1; Test Name: fever; Result Unstructured Data: Test Result:100.1; Comments: she got a low grade fever of 100-100.1; Test Name: Covid-19 test; Test Result: Negative ; Comments: Tested negative after a couple days; Test Date: 20230411; Test Name: Covid-19 test; Test Result: Positive ; Comments: She was positive for COVID again on 11Apr2023.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cough; Heart disorder; Immunocompromised; Joint replacement; Rheumatoid arthritis; Surgery
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2617161

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: VA
Alter: -
Geschlecht: M
Eingang: 19.04.2023
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 5
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 positive after receiving Pfizer COVID-19 Vaccinations; COVID-19 positive after receiving Pfizer COVID-19 Vaccinations; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), as dose 5 (booster), single (Lot number: GJ3275) for covid-19 immunisation; BNT162b2 (BNT162B2), as dose 4 (booster), single (Batch/Lot number: unknown), as dose 3 (booster), single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 1, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "heart issue" (unspecified if ongoing), notes: he's a heart patient; "immunocompromised" (unspecified if ongoing), notes: she is immunocompromised. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19 positive after receiving Pfizer COVID-19 Vaccinations". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: back in Dec (date incomplete); Negative, notes: Tested negative after a couple days. Therapeutic measures were taken as a result of drug ineffective, covid-19. 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: SARS-CoV-2 test; Test Result: Positive; Comments: back in Dec (date incomplete); Test Name: tested; Test Result: Negative; Comments: Tested negative after a couple days.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Heart disorder (he's a heart patient); Immunocompromised (she is immunocompromised.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2616486

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OH
Alter: -
Geschlecht: F
Eingang: 18.04.2023
Impfdatum: 14.12.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / LA

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

COVID-19 Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; 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 74-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Dec2022 at 13:00 as dose 4 (booster), single (Lot number: GJ3275), in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 03Mar2021 as dose 1, single (Lot number: EL9266), on 24Mar2021 as dose 2, single (Lot number: EN3518) and on 26May2022 at 13:00 as dose 3 (booster), single (Lot number: FJ4989), in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19 which included Paxlovid.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300154212 Same reporter/patient,different drug/AE;

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, Comment: Other medical history: None Known allergies: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2609545

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ3275

gering

Staat: CO
Alter: 71,0
Geschlecht: F
Eingang: 04.04.2023
Impfdatum: 26.10.2022
Beginn: 28.11.2022
Tage bis Beginn: 33,0
Dosis: 5
Route/Site: IM / LA

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

Erythema Periorbital swelling Skin texture abnormal

Symptomtext

My eye (above my eye) starting swallow and turn red, got bumpy, in both edges. I went to the urgent care and prescribed steroids medicine plus the cream, and I used that for 5 days, it mostly cleared up after a few days. .

Weitere VAERSDATA-Felder

Praegender Schweregrund: Erythema
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Acyclovir; Losartan; Aspirin
Allergien: N/A
Vorherige Impfungen: -

VAERS 2609341

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: FL
Alter: 77,0
Geschlecht: M
Eingang: 04.04.2023
Impfdatum: 28.10.2022
Beginn: 01.04.2023
Tage bis Beginn: 155,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

patient hospitalized

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2608266

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: PA
Alter: 73,0
Geschlecht: F
Eingang: 03.04.2023
Impfdatum: 20.10.2022
Beginn: 16.11.2022
Tage bis Beginn: 27,0
Dosis: 4
Route/Site: - / -

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

Anxiety COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

I experienced a breakthrough case of COVID-19 with me being very anxious and having anxiety.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anxiety
Hospital-Tage: -
Labordaten: 16Nov2022 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Amlodipine; losartan; statin; SYNTHROID
Allergien: N/A
Vorherige Impfungen: -

VAERS 2564132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: -
Alter: 84,0
Geschlecht: U
Eingang: 31.03.2023
Impfdatum: 13.12.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / LA

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

Drug ineffective Suspected COVID-19 Tinnitus

Symptomtext

After shot 5, I had COVID; After shot 5, I had COVID; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. An 84-year-old patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 13Dec2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 84 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 13Jan2021 as dose 1, single (Lot number: EL3249) intramuscular, in left arm, on 30Jan2021 as dose 2, single (Lot number: EN5318), in left arm, on 01Sep2021 as dose 3 (booster), single (Lot number: FC3183), in left arm and on 09May2022 as dose 4 (booster), single (Lot number: FM9992), in left arm 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), SUSPECTED COVID-19 (medically significant), outcome "unknown" and all described as "After shot 5, I had COVID". No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300024573 same patient, different vaccine dose/event;

Weitere VAERSDATA-Felder

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

VAERS 2564132

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: -
Alter: 84,0
Geschlecht: U
Eingang: 31.03.2023
Impfdatum: 13.12.2022
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: - / -

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

Drug ineffective Suspected COVID-19 Tinnitus

Symptomtext

After shot 5, I had COVID; After shot 5, I had COVID; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. An 84-year-old patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 13Dec2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 84 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 13Jan2021 as dose 1, single (Lot number: EL3249) intramuscular, in left arm, on 30Jan2021 as dose 2, single (Lot number: EN5318), in left arm, on 01Sep2021 as dose 3 (booster), single (Lot number: FC3183), in left arm and on 09May2022 as dose 4 (booster), single (Lot number: FM9992), in left arm 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), SUSPECTED COVID-19 (medically significant), outcome "unknown" and all described as "After shot 5, I had COVID". No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300024573 same patient, different vaccine dose/event;

Weitere VAERSDATA-Felder

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

VAERS 2605671

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: CA
Alter: 61,0
Geschlecht: F
Eingang: 29.03.2023
Impfdatum: 03.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
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). The reporter is the patient. A 62-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 03Nov2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 61 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 08Mar2021 as dose 1, single (Lot number: EN6206), in left arm, on 29Mar2021 as dose 2, single (Lot number: ER8732), in left arm, on 19Nov2021 as dose 3 (booster), single (Lot number: FF8841), in left arm and on 14Jun2022 as dose 4 (booster), single (Lot number: FM7553), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Celiac" (unspecified if ongoing). The patient's concomitant medications were not reported. No known allergies. 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 (COVID 19 Treatment) from 20Mar2023 to 21Mar2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Celiac disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2604372

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: CA
Alter: 27,0
Geschlecht: F
Eingang: 28.03.2023
Impfdatum: 10.11.2022
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

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 27-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Nov2022 as dose 4 (booster), single (Lot number: GJ3275) at the age of 27 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 09Mar2021 as dose 1, single (Lot number: GN6205), in right arm, on 29Mar2021 as dose 2, single (Lot number: GR8732) and on 26Jan2022 as dose 3 (booster), single (Batch/Lot number: unknown), in right arm for covid-19 immunisation. The patient's relevant medical history included: "ADHD" (unspecified if ongoing), notes: other medical history: ADHD; "bronchiectasis" (unspecified if ongoing), notes: other medical history: bronchiectasis; "pectus excavatum" (unspecified if ongoing), notes: other medical history: pectus excavatum; "unspecified chronic lung disease" (unspecified if ongoing), notes: other medical history: unspecified chronic lung disease; "dysmenorrhea" (unspecified if ongoing), notes: other medical history: dysmenorrhea; "suspected endometriosis" (unspecified if ongoing), notes: other medical history: suspected endometriosis; "known allergies: Shellfish" (unspecified if ongoing), notes: known allergies: Shellfish. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "recovered" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. 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: Medical History/Concurrent Conditions: ADHD (other medical history: ADHD); Bronchiectasis (other medical history: bronchiectasis); Chronic lung disease (other medical history: unspecified chronic lung disease); Dysmenorrhea (other medical history: dysmenorrhea); Endometriosis (other medical history: suspected endometriosis); Pectus excavatum (other medical history: pectus excavatum); Shellfish allergy (known allergies: Shellfish)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2603408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: KY
Alter: 50,0
Geschlecht: F
Eingang: 24.03.2023
Impfdatum: 22.12.2022
Beginn: 11.03.2023
Tage bis Beginn: 79,0
Dosis: 5
Route/Site: IM / RA

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

Allergic cough COVID-19 Nasal congestion Nasopharyngitis Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Sick relative

Symptomtext

My spouse was positive on the preceding Tuesday. I felt like I had a cold congestion in my nose and head. I had like a allergy cough, and sniffles. I tested positive on Thursday morning. I called my doctor and was prescribed PAXLOVID. My symptoms were better by Monday. I still have a cough; I don't know if its allergies or lingering symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Allergic cough
Hospital-Tage: -
Labordaten: 11MAR2023 COVID-19 test positive
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: ALLEGRA
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2600203

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: KY
Alter: 18,0
Geschlecht: F
Eingang: 21.03.2023
Impfdatum: 17.03.2023
Beginn: 01.03.2023
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Online appointment was requested on pharmacy site. Indicated first initial shot of COVID vaccination for my daughter. Appointment was made for 3/17 at 2:15 pm. We were able to select no previous vaccinations and this was 1st shot for the location. Arrived at pharmacy and was administered Bivalent vaccination instead of monovalent. Conversation with vaccinating staff mentioned this was the initial vaccination. No adverse side effects. Communicated with health department on 3/20 after realizing that booster vaccine was given instead of original vaccine. Advised no side effects to be expected and to continue with 2nd initial vaccination not repeating original monovalent dose. Discussed with pharmacy location Pharmacist on 3/20 that website allowed initial vaccination and staff administered bivalent vaccine in error.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Cryselle 0.3mg/0.03mg, Zyrtec, and Flonaise
Allergien: Outdoor allergies
Vorherige Impfungen: -

VAERS 2598239

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: NC
Alter: 60,0
Geschlecht: F
Eingang: 17.03.2023
Impfdatum: 24.10.2022
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

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Nurse). 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 24Oct2022 as dose 4 (booster), single (Lot number: GJ3275) at the age of 60 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 18Mar2021 as dose 1, single (Lot number: ER2613), in right arm, on 08Apr2021 as dose 2, single (Lot number: EW0151), in left arm and on 11Nov2021 as dose 3 (booster), single (Lot number: FH8028), in right arm for covid-19 immunisation. The patient's relevant medical history included: "PVCs" (unspecified if ongoing); "PACs" (unspecified if ongoing); "hx histoplasmosis with multiple nodules both lungs" (unspecified if ongoing); "chronic cough" (unspecified if ongoing); "known allergies: Penicillin" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (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: (Mar2023) Positive, notes: Tested positive for Covid 5 days after finishing paxlovid. Therapeutic measures were taken as a result of vaccination failure, covid-19 with Paxlovid from 05Mar2023 to 09Mar2023.; Sender's Comments: The efficacy of a product varies from one patient to another and can be affected by different factors; however, based on the temporal association and available information, a causal relationship between the events and suspect vaccine cannot be completely excluded.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 202303; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Tested positive for Covid 5 days after finishing paxlovid.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Chronic cough; Histoplasmosis; Penicillin allergy; Premature atrial contraction; Premature ventricular contractions
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2596241

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MI
Alter: 82,0
Geschlecht: F
Eingang: 14.03.2023
Impfdatum: 01.12.2022
Beginn: 18.12.2022
Tage bis Beginn: 17,0
Dosis: 4
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 4 vaccines Moderna 1/21/21 Lot# 012L20A; Moderna 2/18/21 Lot# 016M20A; Moderna 11/12/21 Lot# 013F21A; Pfizer 12/1/22 Lot# GJ3275

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2594303

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: -
Alter: 37,0
Geschlecht: M
Eingang: 10.03.2023
Impfdatum: 16.10.2022
Beginn: 04.12.2021
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

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

COVID-19 Interchange of vaccine products Vaccination failure

Symptomtext

COVID-19; COVID-19; Vaccine brand other=Moderna/ vaccine brand=Pfizer / BioNTech; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 38-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 16Oct2022 as dose 4 (booster), single (Lot number: GJ3275) at the age of 37 years for covid-19 immunisation; BNT162b2 (BNT162B2), on 13Mar2021 as dose 1, single (Lot number: EN6208) and on 02Apr2021 as dose 2, single (Lot number: EW0151) for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 04Dec2021 as dose 3 (booster), single (Lot number: 024C21A) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 04Dec2021, outcome "unknown", described as "Vaccine brand other=Moderna/ vaccine brand=Pfizer / BioNTech"; VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Feb2023, outcome "unknown" and all described as "COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19 which included COVID-19 Treatment form 24Feb2023 to 01Mar2023. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2592708

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: MI
Alter: 65,0
Geschlecht: F
Eingang: 08.03.2023
Impfdatum: 07.11.2022
Beginn: 07.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 Drug ineffective Interchange of vaccine products

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; Moderna, Date: 14Jul2022 ; Pfizer / BioNTech, Date: 07Nov2022; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 66-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 07Nov2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 65 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 12Mar2021 as dose 1, single (Lot number: 010A21A), in left arm, on 07Apr2021 as dose 2, single (Lot number: 018B21A), in left arm, on 30Nov2021 as dose 3 (booster), single (Lot number: EW0183), in left arm and on 14Jul2022 as dose 4 (booster), single (Lot number: 016B22A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Irritable Bowel syndrome" (unspecified if ongoing); "interstitial cystitis" (unspecified if ongoing); "Known allergies: Sulfa drugs" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Ibuprofen, reaction(s): "Known allergies:Ibuprofen". The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 07Nov2022, outcome "unknown", described as "Moderna, Date: 14Jul2022 ; Pfizer / BioNTech, Date: 07Nov2022"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Additional information: patient received COVID 19 Treatment: PAXLOVID from 22Feb2023 to 27Feb2023 as Treatment of COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Cystitis interstitial; Irritable bowel syndrome; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2589261

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MI
Alter: 80,0
Geschlecht: M
Eingang: 01.03.2023
Impfdatum: 02.11.2022
Beginn: 28.02.2023
Tage bis Beginn: 118,0
Dosis: 5
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID vaccine breakthrough case. Pfizer 2/28/21 EN6202, 3/21/21 EN6207, 11/3/21 FE3590, 5/27/22 FM0173, and bivalent 11/2/23 GJ3275.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Positive COVID test on 2/28/23
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2585942

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: NC
Alter: 39,0
Geschlecht: M
Eingang: 23.02.2023
Impfdatum: 31.01.2023
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / LA

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

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 39-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 31Jan2023 as dose 5 (booster), single (Lot number: GJ3275) at the age of 39 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 12Apr2021 as dose 1, single (Lot number: ER8734), in left arm, on 03May2021 as dose 2, single (Lot number: EN0162), in left arm, on 18Nov2021 as dose 3 (booster), single (Lot number: FH8027), in left arm and on 28Sep2022 as dose 4 (booster), single (Lot number: FP7138), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: All the cillins" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive; (Feb2023) negative, notes: tested negative then at day 4 after my series was completed; (Feb2023) positive, notes: tested positive for covid again; so a rebound. Therapeutic measures were taken as a result of drug ineffective, covid-19 which included Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Test; Test Result: Positive ; Test Date: 202302; Test Name: COVID-19 Test; Test Result: Negative ; Comments: tested negative then at day 4 after my series was completed.; Test Date: 202302; Test Name: COVID-19 Test; Test Result: Positive ; Comments: tested positive for covid again; so a rebound.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2585907

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: TN
Alter: 70,0
Geschlecht: F
Eingang: 23.02.2023
Impfdatum: 15.11.2022
Beginn: 22.12.2022
Tage bis Beginn: 37,0
Dosis: 5
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 positive test date was on 22Dec2022; covid positive test date was on 22Dec2022; The initial case was missing the following minimum criteria: no adverse effect. Upon receipt of follow-up information on (16Feb2023), this case now contains all required information to be considered valid. 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 received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 15Nov2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 70 years, in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 28Jan2021 as dose 1, single (Lot number: EL8982) intramuscular, in right arm, on 18Feb2021 as dose 2, single (Lot number: EM9809) intramuscular, in right arm, on 19Oct2021 as dose 3 (booster), single (Lot number: FE3590) intramuscular, in right arm and on 23May2022 as dose 4 (booster), single (Lot number: FK9893), in right arm for covid-19 immunisation. The patient's relevant medical history included: "Arthroscopic surgery" (unspecified if ongoing), notes: Arthroscopic surgery in left arm, previously. The patient's concomitant medications were not reported. Vaccination history included: Flu shot (Vaccine name: Flu shot, Anatomical Site of Injection: Right Arm, Number of Previous Doses: (One per year)), for Immunization. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 22Dec2022, outcome "unknown" and all described as "covid positive test date was on 22Dec2022". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (22Dec2022) Positive, notes: covid positive test. Clinical course: The patient had received 5 vaccines in total. The patient had all of her COVID Boosters in right arm because of arthroscopic surgery in left arm, previously. Her right arm felt great until the 15Nov2022 booster given. Reporter stated the covid positive test date was on 22Dec2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20221222; Test Name: Covid-19 test; Test Result: Positive ; Comments: covid positive test
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Arthroscopic surgery (Arthroscopic surgery in left arm, previously.)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2583910

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 18.02.2023
Impfdatum: 24.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
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 a contactable reporter(s) (Nurse). The reporter is the patient. A 63-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 24Oct2022 at 12:30 as dose 5 (booster), single (Lot number: GJ3275) at the age of 62 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 22Dec2020 as dose 1, single (Lot number: EH9899), in left arm, on 14Jan2021 at 11:45 as dose 2, single (Lot number: EL3246), in left arm, on 05Oct2021 at 16:00 as dose 3 (booster), single (Lot number: CJ511-06), in left arm and on 08Apr2022 at 09:30 as dose 4 (booster), single (Lot number: FK9894), in left arm for covid-19 immunisation. The patient's relevant medical history included: "hypertension" (unspecified if ongoing); "obesity" (unspecified if ongoing); "elevated intraocular pressure" (unspecified if ongoing); "lobster" (unspecified if ongoing); "mango" (unspecified if ongoing); "vomit" (unspecified if ongoing); "diarrhea" (unspecified if ongoing); "nausea" (unspecified if ongoing); "rash" (unspecified if ongoing). Concomitant medication(s) included: LATANOPROST, start date: 22Aug2022. Past drug history included: Tetracycline, reaction(s): "G.i"; Fentanyl, reaction(s): "Nausea"; Fentanyl, reaction(s): "Vomit"; Fentanyl, reaction(s): "itch". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "recovering" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19.; Sender's Comments: The efficacy of a vaccine varies individually and can be affected by different factors including product potency; however, a contributory role of BNT162B2 and BNT162b2, BNT162b2 omi ba.4-5 to vaccination failure cannot be ruled out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Diarrhea; Fruit allergy; Hypertension; Intraocular pressure; Nausea; Obesity; Rash; Seafood allergy; Vomiting
Andere Medikamente: LATANOPROST
Allergien: -
Vorherige Impfungen: -

VAERS 2524233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: SC
Alter: 21,0
Geschlecht: F
Eingang: 17.02.2023
Impfdatum: 12.11.2022
Beginn: 12.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Incorrect product formulation administered Nasopharyngitis

Symptomtext

ADMINSITRATION ERROR: She was given a COVID booster instead of her first does. Had cold symptoms for a month after the vaccine. Currently she does not have a no symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: yes, obelion 30 ER, abilify 10 mg
Allergien: none
Vorherige Impfungen: -

VAERS 2524233

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: SC
Alter: 21,0
Geschlecht: F
Eingang: 17.02.2023
Impfdatum: 12.11.2022
Beginn: 12.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Incorrect product formulation administered Nasopharyngitis

Symptomtext

ADMINSITRATION ERROR: She was given a COVID booster instead of her first does. Had cold symptoms for a month after the vaccine. Currently she does not have a no symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: yes, obelion 30 ER, abilify 10 mg
Allergien: none
Vorherige Impfungen: -

VAERS 2582347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 15.02.2023
Impfdatum: 21.12.2022
Beginn: 03.01.2023
Tage bis Beginn: 13,0
Dosis: 5
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 5 vaccines Moderna 3/19/21 Lot# 006B21A; Modern a4/16/21 Lot# 043B21A; Moderna 2/8/21 Lot# 029H21B; Moderna 4/13/22 Lot# 002M21A; Pfizer 12/21/22 LOt# GJ3275

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2582044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: WI
Alter: 69,0
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 01.11.2022
Beginn: 01.01.2023
Tage bis Beginn: 61,0
Dosis: 6
Route/Site: - / RA

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

COVID-19 Drug ineffective

Symptomtext

Paxlovid as Treatment of COVID-19; Paxlovid as Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 69-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 01Nov2022 at 12:00 as dose 6 (booster), single (Lot number: GJ3275) at the age of 69 years, in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 05Mar2021 at 10:00 as dose 1, single (Lot number: EN6205), in left arm, on 26Mar2021 at 10:15 as dose 2, single (Lot number: ER8732), in left arm, on 18Aug2021 at 09:30 as dose 3 (booster), single (Lot number: FC3180), in left arm, on 24Jan2022 at 13:00 as dose 4 (booster), single (Lot number: 33025BD), in right arm and on 13Jun2022 at 10:00 as dose 5 (booster), single (Lot number: FN2908), in right arm for covid-19 immunisation. The patient's relevant medical history included: "Sarcoidosis" (unspecified if ongoing); "High Blood Pressure" (unspecified if ongoing); "Hypothyroidism" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Diltiazem, reaction(s): "Known allergies: Diltiazem"; Lisinopril, reaction(s): "Known allergies: Lisinopril". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Jan2023, outcome "unknown" and all described as "Paxlovid as Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19 including Paxlovid from 31Jan2023 to 05Feb2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Blood pressure high; Hypothyroidism; Sarcoidosis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2582008

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: TN
Alter: 22,0
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 19.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: - / LA

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

Tinnitus

Symptomtext

I began to experience Pulsatile Tinnitus in my right ear; 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 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 19Nov2022 as dose 4 (booster), single (Lot number: GJ3275) at the age of 22 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Migraines" (unspecified if ongoing); "Anxiety" (unspecified if ongoing); "Convergence insufficiency" (unspecified if ongoing); "If COVID prior vaccination: Yes" (unspecified if ongoing), notes: If COVID prior vaccination: Yes. The patient's concomitant medications were not reported. Past drug history included: Clindamycin, reaction(s): "known allergies: Clindamycin", notes: known allergies: Clindamycin. Vaccination history included: Covid-19 vaccine (Dose number: 1, Manufacturer: Unknown), for COVID-19 immunization; Covid-19 vaccine (Dose number: 2, Manufacturer: Unk2own), for COVID-19 immunization; Covid-19 vaccine (Dose number: 3, Manufacturer: Unknown), for COVID-19 immunization. The following information was reported: TINNITUS (non-serious) with onset 22Nov2022 at 12:00, outcome "not recovered", described as "I began to experience Pulsatile Tinnitus in my right ear". The event "i began to experience pulsatile tinnitus in my right ear" required physician office visit. Therapeutic measures were not taken as a result of tinnitus. Additional information: The patient had COVID prior vaccination. The patient had not COVID tested post vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; Convergence insufficiency; COVID-19 (If COVID prior vaccination: Yes); Migraine
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2582007

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 69,0
Geschlecht: F
Eingang: 15.02.2023
Impfdatum: 13.11.2022
Beginn: 01.01.2023
Tage bis Beginn: 49,0
Dosis: 5
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

COVID-19; COVID-19; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from product quality group. The reporter is the patient. A 69-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 13Nov2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 69 years for covid-19 immunisation; BNT162b2 (BNT162B2), on 22Jan2021 at 12:00 as dose 1, single (Lot number: EL3246), on 16Feb2021 at 13:00 as dose 2, single (Lot number: EL3246), on 13Oct2021 as dose 3 (booster), single (Lot number: FF2589) and on 11Apr2022 as dose 4 (booster), single (Lot number: FJ9943) for covid-19 immunisation. The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Jan2023, outcome "not recovered" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: I took a Covid test that was again positive; Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient treatment of Paxlovid started on 25Jan2023 and stopped on 30Jan2023, lot number: GF3965. No known allergies.; Sender's Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the events and BNT162B2.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive ; Comments: I took a Covid test that was again positive.; Test Name: Covid-19 test; Test Result: Positive ; Comments: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: other medical history: None
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2578581

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 31,0
Geschlecht: F
Eingang: 09.02.2023
Impfdatum: 11.10.2022
Beginn: 01.01.2023
Tage bis Beginn: 82,0
Dosis: 4
Route/Site: - / -

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

COVID-19 Vaccination failure

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Other HCP) from product quality group. The reporter is the patient. A 32-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 11Oct2022 as dose 4 (booster), single (Lot number: GJ3275) at the age of 31 years for covid-19 immunisation; BNT162b2 (BNT162B2), on 27Dec2020 as dose 1, single (Lot number: EK9231), on 16Jan2021 as dose 2, single (Lot number: EL3247) and on 05Oct2021 as dose 3 (booster), single (Lot number: EW0217) for covid-19 immunisation. The patient's relevant medical history included: "Pregnant" (unspecified if ongoing), notes: Other medical history: Pregnant; "known allergies: Sulfa" (unspecified if ongoing). Concomitant medication(s) included: BUPROPION, start date: 01Oct2021. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Jan2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19: Paxlovid .; Sender's Comments: Based on the information provided, a causal relationship between the suspected drug and the reported events Vaccination failure , COVID-19 cannot be excluded

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Pregnant (Other medical history: Pregnant); Sulfonamide allergy
Andere Medikamente: BUPROPION
Allergien: -
Vorherige Impfungen: -

VAERS 2574351

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MO
Alter: 59,0
Geschlecht: M
Eingang: 02.02.2023
Impfdatum: 01.11.2022
Beginn: 30.12.2022
Tage bis Beginn: 59,0
Dosis: UNK
Route/Site: IM / AR

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

Unevaluable event

Symptomtext

None

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, pre-diabetes, hyperlipidemia
Andere Medikamente: Metoprolol tartrate, metformin, clonidine, Amlodipine, pravastatin, Maxzide, Effexor HR, multivitamin for men 50+, fish oil, Zyrtec.
Allergien: None
Vorherige Impfungen: -

VAERS 2568829

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CT
Alter: 57,0
Geschlecht: F
Eingang: 26.01.2023
Impfdatum: 15.12.2022
Beginn: 15.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Eye laser surgery Laboratory test Retinal tear Vitreous detachment Vitreous haemorrhage

Symptomtext

Patient had hemorrhagic vitreous detachment, retinal tear. Treatment was laser surgery and rest. Outcome was back to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye laser surgery
Hospital-Tage: -
Labordaten: Multiple optical tests 12/15/22, 12/20/22
Aktuelle Erkrankungen: No
Vorgeschichte: none
Andere Medikamente: Escitalopram 10mg, Rosuvastatin 5mg
Allergien: NKDA Tree nut allergy
Vorherige Impfungen: -

VAERS 2567254

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: CA
Alter: 79,0
Geschlecht: F
Eingang: 25.01.2023
Impfdatum: 17.11.2022
Beginn: 17.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: - / RA

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

Asthenia Extra dose administered Feeling abnormal Interchange of vaccine products SARS-CoV-2 test Sleep disorder

Symptomtext

Dose number: 5, Brand: Pfizer / Dose number: 4, Product: Moderma; Unusual weakness, sleeping longer hours, all over feeling strange.; Unusual weakness, sleeping longer hours, all over feeling strange.; Unusual weakness, sleeping longer hours, all over feeling strange.; Extra Dose Administered; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 79-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 17Nov2022 at 14:30 as dose 5 (booster), single (Lot number: GJ3275) at the age of 79 years, in right arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 17Nov2022 as dose 4 (booster), single (Lot number: 054A22A), in right arm for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Penicillin" (unspecified if ongoing), notes: Known allergies: Penicillin. Concomitant medication(s) included: CRESTOR; HYDRALAZINE; XARELTO. Past drug history included: Codine, reaction(s): "Known allergies: Codine", notes: Known allergies: Codine. Vaccination history included: Covid-19 vaccine (DOSE 1, Manufacturer unknown), for COVID-19 immunization; Covid-19 vaccine (DOSE 2, Manufacturer unknown), for COVID-19 immunization; Covid-19 vaccine (DOSE 3, Manufacturer unknown), for COVID-19 immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (hospitalization, life threatening) with onset 17Nov2022 at 14:30, outcome "unknown", described as "Dose number: 5, Brand: Pfizer / Dose number: 4, Product: Moderma"; EXTRA DOSE ADMINISTERED (non-serious) with onset 17Nov2022 at 14:30, outcome "unknown"; ASTHENIA (caused and prolonged hospitalization, life threatening), SLEEP DISORDER (caused and prolonged hospitalization, life threatening), FEELING ABNORMAL (caused and prolonged hospitalization, life threatening) all with onset 20Nov2022 at 12:00, outcome "recovered with sequelae" and all described as "Unusual weakness, sleeping longer hours, all over feeling strange.". The patient was hospitalized and prolonged hospitalization for asthenia, sleep disorder, feeling abnormal (hospitalization duration: 25 day(s)). The event "unusual weakness, sleeping longer hours, all over feeling strange." required emergency room visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (16Dec2022) Negative, notes: COVID test name post vaccination: In hospital. Therapeutic measures were taken as a result of asthenia, sleep disorder, feeling abnormal. Clinical information: Patient had not received other vaccines in four weeks. Other medication in two weeks: Crestor, Hydralazine, Xarelto. AE treatment: new meds and therapy. No COVID prior vaccination, COVID tested post vaccination: yes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: -
Labordaten: Test Date: 20221216; Test Name: Nasal swab; Test Result: Negative ; Comments: COVID test name post vaccination: In hospital
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Penicillin allergy (Known allergies: Penicillin)
Andere Medikamente: CRESTOR; HYDRALAZINE; XARELTO
Allergien: -
Vorherige Impfungen: -

VAERS 2566723

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ3275

gering

Staat: MO
Alter: 86,0
Geschlecht: F
Eingang: 24.01.2023
Impfdatum: 06.11.2022
Beginn: 16.01.2023
Tage bis Beginn: 71,0
Dosis: 5
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

unable to interview case due to hospitalization

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: Unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2563289

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: AR
Alter: 93,0
Geschlecht: F
Eingang: 19.01.2023
Impfdatum: 25.10.2022
Beginn: 11.01.2023
Tage bis Beginn: 78,0
Dosis: 5
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test positive Thermal burn

Symptomtext

hospitalized with covid; fully vaccinated with 3 boosters

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 2,0
Labordaten: positive covid pcr 1/7/23
Aktuelle Erkrankungen: unknown
Vorgeschichte: Coronary Artery Disease (negative cardiac catherization 2013), Congestive Heart Failure, Hyperlipidemia, Hypertension, Reflux and Other (A-fib-major burn trauma in past)
Andere Medikamente: unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2562409

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 23,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 16.01.2023
Beginn: 16.01.2023
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Muscle contractions involuntary

Symptomtext

Involuntary & uncontrollable muscle contractions. Was only bad for several minutes, occurred several times over a few hours

Weitere VAERSDATA-Felder

Praegender Schweregrund: Muscle contractions involuntary
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Lamotrigine, fluvoxamine, naltrexone
Allergien: Thorazine, lithium
Vorherige Impfungen: Similar muscle contractions dose 2 (2/17/21) and dose 3 (12/2/21)

VAERS 2559970

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: WA
Alter: 50,0
Geschlecht: F
Eingang: 14.01.2023
Impfdatum: 12.12.2022
Beginn: -
Tage bis Beginn: -
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

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 50-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 12Dec2022 at 17:45 as dose 4 (booster), single (Lot number: GJ3275) at the age of 50 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: "Rheumatoid arthritis" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Ibuprofen, reaction(s): "Known allergies: Ibuprofen", notes: Known allergies: Ibuprofen; Methotrexate, reaction(s): "Known allergies: Methotrexate", notes: Known allergies: Methotrexate. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment; Negative, notes: I originally started testing negative on day 8-11; Negative, notes: I originally started testing negative on day 8-11; Negative, notes: I originally started testing negative on day 8-11; Negative, notes: I originally started testing negative on day 8-11; Positive, notes: Tested on day 13 from original positive test and tested Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. The patient received anti-viral Paxlovid for COVID 19 Treatment from 29Dec2022 to 03Jan2023.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19 test; Test Result: Positive ; Comments: COVID 19 Treatment; Test Name: Covid-19 test; Test Result: Negative ; Comments: I originally started testing negative on day 8-11; Test Name: Covid-19 test; Test Result: Negative ; Comments: I originally started testing negative on day 8-11; Test Name: Covid-19 test; Test Result: Negative ; Comments: I originally started testing negative on day 8-11; Test Name: Covid-19 test; Test Result: Negative ; Comments: I originally started testing negative on day 8-11; Test Name: Covid-19 test; Test Result: Positive ; Comments: Tested on day 13 from original positive test and tested Positive.
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Rheumatoid arthritis
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2558545

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: MI
Alter: 70,0
Geschlecht: F
Eingang: 12.01.2023
Impfdatum: 04.11.2022
Beginn: 07.01.2023
Tage bis Beginn: 64,0
Dosis: 4
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID vaccine breakthrough case. Moderna 3/24/21 047A21A, 4/21/21 040B21A and boosted Pfizer 2/11/22 FD2718, 11/4/22 GJ3275

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Positive COVID test on 1/7/23
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2557622

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CT
Alter: 49,0
Geschlecht: F
Eingang: 11.01.2023
Impfdatum: 10.01.2023
Beginn: 11.01.2023
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Expired product administered

Symptomtext

Gave patient an expired dose that was 5 days passed expiration date

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2556198

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: AZ
Alter: 35,0
Geschlecht: F
Eingang: 10.01.2023
Impfdatum: 13.11.2022
Beginn: 08.12.2022
Tage bis Beginn: 25,0
Dosis: 4
Route/Site: IM / LA

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

Pityriasis rosea

Symptomtext

Pytiriasis rosea, started around Dec 8, remains present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pityriasis rosea
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: Type 1 diabetes
Andere Medikamente: Humalog insulin
Allergien: None
Vorherige Impfungen: -

VAERS 2551905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: CA
Alter: 62,0
Geschlecht: F
Eingang: 06.01.2023
Impfdatum: 21.10.2022
Beginn: 21.12.2022
Tage bis Beginn: 61,0
Dosis: 5
Route/Site: - / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 62-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 21Oct2022 as dose 5 (booster), single (Lot number: GJ3275) at the age of 62 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 07Mar2021 as dose 1, single (Batch/Lot number: unknown), in left arm, on 29Mar2021 as dose 2, single (Lot number: EP6955), in left arm, on 29Oct2021 as dose 3 (booster), single (Lot number: FE3590), in left arm and on 04May2022 as dose 4 (booster), single (Lot number: FK9893), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Migraines" (unspecified if ongoing); "IBS/IBD" (unspecified if ongoing); "Depression" (unspecified if ongoing). Concomitant medication(s) included: WELLBUTRIN, start date: Jan2010; CYMBALTA, start date: Jan2018; TROKENDI XR, start date: Jan2012; OMEPRAZOLE, start date: Apr2012; FISH OIL, start date: Jan2018; MAGNESIUM, start date: Jan2018; ALIGN, start date: Jan2000. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 21Dec2022, outcome "not recovered" and all described as "COVID 19 Treatment/tested positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive; (21Dec2022) Positive, notes: 1st tested positive 21Dec with symptoms; (24Dec2022) negative, notes: Tested negative on 24Dec; (31Dec2022) Positive, notes: 31Dec - Tested positive again; (02Jan2023) Positive, notes: 02Jan still positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. 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 TEST; Test Result: Positive ; Test Date: 20221221; Test Name: COVID TEST; Test Result: Positive ; Comments: 1st tested positive 21Dec with symptoms; Test Date: 20221224; Test Name: COVID TEST; Test Result: Negative ; Comments: Tested negative on 24Dec; Test Date: 20221231; Test Name: COVID TEST; Test Result: Positive ; Comments: 31Dec - Tested positive again; Test Date: 20230102; Test Name: COVID TEST; Test Result: Positive ; Comments: 02Jan still positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Depression; Inflammatory bowel disease; Migraine
Andere Medikamente: WELLBUTRIN; CYMBALTA; TROKENDI XR; OMEPRAZOLE; FISH OIL; MAGNESIUM; ALIGN
Allergien: -
Vorherige Impfungen: -

VAERS 2551284

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: NC
Alter: 75,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 18.11.2022
Beginn: 06.12.2022
Tage bis Beginn: 18,0
Dosis: 5
Route/Site: SYR / LA

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

Cough Lacrimation increased Rhinorrhoea SARS-CoV-2 test negative Sneezing

Symptomtext

12/26/22 I started sneezing, had a runny nose, itchy and runny eyes, and a cough. At first I thought it was allergies, but this seemed different from allergies. The next day, I had the same symptoms, the runny nose was worse. I went to a COVID testing site to take a COVID test. Both the rapid and PCR tests were negative. I figured it was a viral infection. My symptoms did not worsen, and I felt better within a few days. I figured it was just some type of virus.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cough
Hospital-Tage: -
Labordaten: COVID rapid test, negative; COVID PCR test, negative
Aktuelle Erkrankungen: None
Vorgeschichte: Obesity, Hypertension, Hashimoto Thyroiditis
Andere Medikamente: Levothyroxine, Amlodipine, Besylate, Metoprolol Succinate ER, Montelukast Sodium, Loratidine, Vitamin D3, Vitamin B12, Potassium
Allergien: Doxycycline, Paclitaxel, Latex, Shellfish, Bee Stings
Vorherige Impfungen: -

VAERS 2550818

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: OR
Alter: 11,0
Geschlecht: M
Eingang: 04.01.2023
Impfdatum: 16.11.2022
Beginn: 16.11.2022
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

Symptomtext

PATIENT WAS 11 YEARS AND 11 MONTHS AT THE TIME OF ADMINISTRATION. I ASKED THE PATIENT AGE AND WROTE DOWN ON FORM 12 YEARS OLD. I CONTACTED MOTHER OF PATIENT AFTER INCIDENT HAD BEEN DISCOVERED. SHE SAID HE IS FEELING OKAY WITH NO REACTION AT ALL. SHE STATED, "MY SON IS A BIG BOY WEIGHING 140 POUNDS AND IS 6'0 TALL."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE REPORTED
Vorgeschichte: NONE REPORTED
Andere Medikamente: UNKOWN
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2549710

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 04.01.2023
Impfdatum: 04.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 5
Route/Site: - / RA

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

COVID-19 Drug ineffective

Symptomtext

Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 72-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 04Nov2022 at 12:00 as dose 5 (booster), single (Lot number: GJ3275) at the age of 72 years, in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 14Apr2022 as dose 4 (booster), single (Lot number: FK9893), in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 19Oct2021 as dose 3 (booster), single (Lot number: FH8020), 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: "Known allergies: A few antibiotics" (unspecified if ongoing), notes: Known allergies: A few antibiotics. Concomitant medication(s) included: TYLENOL, start date: Nov2022, stop date: Dec2022. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19 with PAXLOVID. Additional information: Anti-Viral Details: Product=COVID 19 Treatment, Brand=PAXLOVID, Treatment Start Date=01Dec2022, Treatment Stop Date=05Dec2022, Indication=Treatment Of COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to antibiotic (Known allergies: A few antibiotics.)
Andere Medikamente: TYLENOL
Allergien: -
Vorherige Impfungen: -

VAERS 2547143

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: VA
Alter: 11,0
Geschlecht: U
Eingang: 30.12.2022
Impfdatum: 18.11.2022
Beginn: 18.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Grey bivalent given upon charting realized that orange should have been given. Provider and family notified.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2544260

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 28.12.2022
Impfdatum: 19.11.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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

COVID-19 Drug ineffective SARS-CoV-2 test

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 47-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 19Nov2022 at 09:45 as dose 4 (booster), single (Lot number: GJ3275) at the age of 47 years, in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 24Nov2021 as dose 3 (booster), single (Lot number: FJ1620), in right 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: "Asthma" (unspecified if ongoing). There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Positive; (Dec2022) Negative, notes: Day 1; (Dec2022) Negative, notes: Day 4; (Dec2022) Positive, notes: 5 days after end of Paxlovid course. Therapeutic measures were taken as a result of drug ineffective, covid-19. Additional information: No other medication in 2weeks. No known allergies. The patient received Paxlovid for COVID 19 Treatment from 13Dec2022 to 18Dec2022. Positive COVID test with symptoms 5 days after end of Paxlovid course. Negative tests on Day 1 and day 4.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Test; Test Result: Positive ; Test Date: 202212; Test Name: COVID-19 Test; Test Result: Negative ; Comments: Day 1; Test Date: 202212; Test Name: COVID-19 Test; Test Result: Negative ; Comments: Day 4; Test Date: 202212; Test Name: COVID-19 Test; Test Result: Positive ; Comments: 5 days after end of Paxlovid course
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Asthma
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2543999

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: TX
Alter: 34,0
Geschlecht: F
Eingang: 27.12.2022
Impfdatum: 27.12.2022
Beginn: 27.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SC / LA

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

Incorrect product formulation administered

Symptomtext

Wrong vial was grabbed out of the fridge and not properly verified. Patient was supposed to get the Pfizer dose 1 of the original series, but instead received the updated booster. No signs or symptoms prior to patient leaving the store.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2542791

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: IL
Alter: 79,0
Geschlecht: M
Eingang: 24.12.2022
Impfdatum: 30.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Error: Dose in Series 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 2540839

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 17.12.2022
Beginn: 17.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Extra dose administered

Symptomtext

Family of five walked-in requesting Pfizer bivalent boosters. Techs confirmed last Pfizer booster doses with patients? digital vaccine cards. Pfizer bivalent vaccines were drawn (by pharmacist) and administered (by intern) to all five family members. However, when billing vaccines, four out of five family members? insurance gave rejected, duplicate claims. A report was ran for each family member and found the four family members already received the Pfizer bivalent booster in September/ October. Pharmacist contacted father of the family to confirm if they did, in fact, receive the bivalent booster in September/ October. The father was not sure what booster they received in September/ October but came in because he ?was watching the news and the news said if it?s been two months since your last booster, you are due for another booster? so he decided to bring his whole family in to get another booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2540817

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 18,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 17.12.2022
Beginn: 17.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Extra dose administered

Symptomtext

Family of five walked-in requesting Pfizer bivalent boosters. Techs confirmed last Pfizer booster doses with patients? digital vaccine cards. Pfizer bivalent vaccines were drawn (by pharmacist) and administered (by intern) to all five family members. However, when billing vaccines, four out of five family members? insurance gave rejected, duplicate claims. A report was ran for each family member and found the four family members already received the Pfizer bivalent booster in September/ October. Pharmacist contacted father of the family to confirm if they did, in fact, receive the bivalent booster in September/ October. The father was not sure what booster they received in September/ October but came in because he ?was watching the news and the news said if it?s been two months since your last booster, you are due for another booster? so he decided to bring his whole family in to get another booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 2540807

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 44,0
Geschlecht: M
Eingang: 22.12.2022
Impfdatum: 17.12.2022
Beginn: 17.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Extra dose administered

Symptomtext

Family of five walked-in requesting Pfizer bivalent boosters. Techs confirmed last Pfizer booster doses with patients? digital vaccine cards. Pfizer bivalent vaccines were drawn (by pharmacist) and administered (by intern) to all five family members. However, when billing vaccines, four out of five family members? insurance gave rejected, duplicate claims. A report was ran for each family member and found the four family members already received the Pfizer bivalent booster in September/ October. Pharmacist contacted father of the family to confirm if they did, in fact, receive the bivalent booster in September/ October. The father was not sure what booster they received in September/ October but came in because he ?was watching the news and the news said if it?s been two months since your last booster, you are due for another booster? so he decided to bring his whole family in to get another booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: NA
Allergien: none
Vorherige Impfungen: -

VAERS 2537337

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 35,0
Geschlecht: F
Eingang: 20.12.2022
Impfdatum: 05.12.2022
Beginn: 17.12.2022
Tage bis Beginn: 12,0
Dosis: 4
Route/Site: IM / AR

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

Atrial fibrillation Blood calcium normal Blood magnesium normal Cardioversion Echocardiogram abnormal Exposure during pregnancy Fibrin D dimer Full blood count normal Laboratory test normal Right ventricular dilatation Ventilation/perfusion scan normal

Symptomtext

Patient developed new-onset atrial fibrillation 12 days after receiving the 4th dose of the COVID Pfizer vaccine. She was 37w3d pregnant with her second child at the time of developing atrial fibrillation. She was otherwise well - no recent illnesses. She converted into normal sinus rhythm after two doses of metoprolol.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atrial fibrillation
Hospital-Tage: 2,0
Labordaten: 12/17/2022: Normal chem 7, CBC, calcium, magnesium 12/18/2022: Echocardiogram showed atrial fibrillation and mild dilation of the right ventricle, otherwise normal 12/19/2022: D-dimer 0.88 ug/ml. Lung perfusion scan was negative for pulmonary embolism
Aktuelle Erkrankungen: None
Vorgeschichte: Factor V Leiden
Andere Medikamente: Lovenox, prenatal vitamins
Allergien: None
Vorherige Impfungen: -

VAERS 2533314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: -
Alter: 80,0
Geschlecht: U
Eingang: 16.12.2022
Impfdatum: 09.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Urinary incontinence

Symptomtext

I have had leakage in urine and like I normally can control it but it seems like it just came out, just ripped out, it was enough that my penis got wet; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 80-year-old patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 09Dec2022 as dose number unknown (booster), single (Batch/Lot number: unknown) at the age of 80 years for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Vaccination history included: Covid-19 vaccine (Primary Immunization series complete; unknown manufacturer), for Covid-19 immunization. The following information was reported: URINARY INCONTINENCE (non-serious) with onset 09Dec2022, outcome "unknown", described as "I have had leakage in urine and like I normally can control it but it seems like it just came out, just ripped out, it was enough that my penis got wet". Additional information: Patient received last COVID shot (clarified as Pfizer COVID-19 Vaccine) on 09Dec2022 (reported as yesterday) and patient really did not have any side effects at all. So far it was only been about 24 hours but one thing patient noticed was, patient took a lot of prescriptions (unspecified medication). So, patient drank a lot of water but it seemed like for the last day patient had not been able to hold urination, it was twice in 24-hour period. Patient had leakage in urine and like patient normally could control it but it seemed like it was, patient did not know how to explain it, it just came out you know, just ripped out. It was not a lot but it was enough that patient's penis got wet. Only twice because patient usually urinated maybe up to 10 times per day. So, patient drank a lot of water with all the medication that patient took. Patient inquired if it was a common thing or was it, of any concern to patient because of the shot. It never happened before. The report was not related to a study or programme. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

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

VAERS 2533204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: IA
Alter: 65,0
Geschlecht: F
Eingang: 15.12.2022
Impfdatum: 14.12.2022
Beginn: 14.12.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

She signed up for a Moderna Bivalent but was given the Pfizer Bivalent in error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2533197

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MI
Alter: 79,0
Geschlecht: M
Eingang: 15.12.2022
Impfdatum: 07.11.2022
Beginn: 14.12.2022
Tage bis Beginn: 37,0
Dosis: 5
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 5 vaccines Pfizer 2/25/21 Lot# EN6200; Pfizer 3/19/21 Lot# EN6207; Pfizer 11/10/21 Lot# FF8841; Pfizer 4/5/22 Lot# FJ9943; Pfizer 11/7/22 Lot#GJ3275

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2527888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: WI
Alter: 40,0
Geschlecht: F
Eingang: 09.12.2022
Impfdatum: 09.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

"Patient was due for 3 vaccines and needed the first dose of COVID Vaccine. The patient was due for the Monovalent COVID-19 vaccine and was mistakenly given the Bivalent dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2527846

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: MI
Alter: 9,0
Geschlecht: M
Eingang: 09.12.2022
Impfdatum: 09.12.2022
Beginn: 09.12.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Incorrect dose administered

Symptomtext

child given 0.2 peds dose of pfizer but injection was for 12 and older

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2527427

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge GJ3275

gering

Staat: CO
Alter: 71,0
Geschlecht: F
Eingang: 08.12.2022
Impfdatum: 19.10.2022
Beginn: 19.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

While vaccinated for bivalent boosters at a care facility - this patient was vaccinated without having a primary series for COVID-19 completed

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2526182

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: OR
Alter: 40,0
Geschlecht: M
Eingang: 07.12.2022
Impfdatum: 10.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

No AE. This is a vaccination error. It was discovered after the fact that patient had never received the initial series of COVID vaccines. He should not have received a booster dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2523204

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: OR
Alter: 66,0
Geschlecht: M
Eingang: 05.12.2022
Impfdatum: 09.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

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

Tinnitus

Symptomtext

Tinnitus started within 24 hours of receiving vaccine. It is current and has been constant since starting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: We are in the process of getting the patient into a specialist for testing.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, Hypertension, BPH w/LUTS, Elevate PSA, Hypothyroidism, Hyperlipidemia, Pre-Diabetes, Monitoring for Longterm anticoagulant use
Andere Medikamente: atorvastatin calcium (tablet) atorvastatin 40 mg Take 1 (one) tablet (40 mg total) by mouth every evening. cyanocobalamin (vitamin B-12) (tablet, sublingual) cyanocobalamin (vitamin B-12) 5,000 mcg Place under the tongue. flaxseed Take
Allergien: None
Vorherige Impfungen: -

VAERS 2522666

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: -
Alter: 29,0
Geschlecht: F
Eingang: 04.12.2022
Impfdatum: 21.11.2022
Beginn: 21.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / -

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

Incorrect product formulation administered

Symptomtext

Patient should have received COVID19 PFIZER UPDATED BOOSTER 12+(BIVALENT) and received COVID19 (PRIZER AGE 12+) GRAY CAP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2522651

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MD
Alter: 82,0
Geschlecht: F
Eingang: 04.12.2022
Impfdatum: 28.11.2022
Beginn: 04.12.2022
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / RA

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

Blister Pemphigoid Tension

Symptomtext

tense bullae consistent with new onset bullous pemphigoid to right upper extremity x3

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blister
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: UTI
Vorgeschichte: hypothyroid CHF neuropathy HTN depression
Andere Medikamente: tylenol metoprolol neurontin MVI synthroid prinivil zoloft cefdinir
Allergien: NSAIDS codeine sulfa GUAIFEN/PHENYLEPHRINE/PPA ASPIRIN
Vorherige Impfungen: -

VAERS 2522228

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: FL
Alter: 26,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 16.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient received Bivalent Booster of Pfizer for the first shot in her primary series. instead of the original Monovalent Vaccine. Patient did not report any Adverse Reactions

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: N/A
Allergien: NKA
Vorherige Impfungen: -

VAERS 2522006

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: NJ
Alter: 19,0
Geschlecht: F
Eingang: 02.12.2022
Impfdatum: 01.12.2022
Beginn: 01.12.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

The patient was to get the second dose Pfizer covid vaccine. Instead patient received Pfizer covid booster vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2520975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CO
Alter: 23,0
Geschlecht: F
Eingang: 01.12.2022
Impfdatum: 29.11.2022
Beginn: 29.11.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Incorrect product formulation administered No adverse event

Symptomtext

Bivalent vaccine given to patient instead of primary series. This was to be the second dose of her primary series. 1st dose 1/20/22. Not immunocompromised. Patient aware of error, no side effects or concerns exhibited.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: unknown
Vorgeschichte: unremarkable
Andere Medikamente: Unknown
Allergien: none
Vorherige Impfungen: -

VAERS 2520023

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 46,0
Geschlecht: M
Eingang: 30.11.2022
Impfdatum: 29.11.2022
Beginn: 30.11.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

The patient received the wrong vaccine; instead of receiving the monovalent dose, they received a bivalent dose as the first dose. No signs or symptoms,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Allergic dermatitis, Vitamin D deficiency, Paget's bone disease.
Vorgeschichte: Chronic Hep C, Essential Hypertension,
Andere Medikamente: -
Allergien: Meloxicam
Vorherige Impfungen: -

VAERS 2519650

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 24.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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 a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 67-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 24Oct2022 at 14:00 as dose 4 (booster), single (Lot number: GJ3275) at the age of 67 years, in right 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: "Polymyalgia Rhuematica" (unspecified if ongoing). There were no concomitant medications. Past drug history included: Lysinopril, reaction(s): "Allergy: Lysinopril". 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: Negative, notes: Rebound after negative for 4 days; Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient did not received other medication in 2 weeks. Anti-viral details: Product: COVID 19 Treatment Paxlovid, Treatment start date on 17Nov2022 and stop date on 21Nov2022. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid-19; Test Result: Negative ; Comments: Rebound after negative for 4 days; Test Name: Covid-19; Test Result: Positive ; Comments: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Polymyalgia rheumatica
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2519616

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 30.11.2022
Impfdatum: 14.11.2022
Beginn: 15.11.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: - / LA

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

Dry mouth Tongue dry

Symptomtext

Dry mouth; Dry tongue; 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 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Nov2022 as dose 5 (booster), single (Lot number: GJ3275) 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. Vaccination history included: Covid-19 vaccine (DOSE 1; MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (DOSE 2; MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (DOSE 3 (BOOSTER); MANUFACTURER UNKNOWN), for COVID-19 Immunization; Covid-19 vaccine (DOSE 4 (BOOSTER); MANUFACTURER UNKNOWN), for COVID-19 Immunization. The following information was reported: DRY MOUTH (non-serious) with onset 15Nov2022, outcome "unknown"; TONGUE DRY (non-serious) with onset 15Nov2022, outcome "unknown", described as "Dry tongue". Therapeutic measures were not taken as a result of dry mouth, tongue dry. Additional information: It was also reported that the patient did receive any other vaccines within 4 weeks prior to the COVID vaccine. Patient did not receive any medications within 2 weeks of vaccination. Prior to vaccination, the patient was not diagnosed with COVID-19 and since the vaccination, the patient had been tested for COVID-19. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202201333363 Same patient, different drug/ AE;

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dry mouth
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 2518801

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MI
Alter: 80,0
Geschlecht: F
Eingang: 29.11.2022
Impfdatum: 15.11.2022
Beginn: 24.11.2022
Tage bis Beginn: 9,0
Dosis: 5
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 5 vaccines Moderna 1/18/21 Lot# 029L20A; Moderna 3/23/21 Lot# 010A21A; Moderna 11/10/21 Lot# 933906; Pfizer 4/4/22 Lot# FK9895; Pfizer 11/15/22 GJ3275

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2518371

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge gj3275

gering

Staat: SC
Alter: 21,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 31.10.2022
Beginn: 31.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2518121

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: WI
Alter: 50,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 13.10.2022
Beginn: 09.11.2022
Tage bis Beginn: 27,0
Dosis: 1
Route/Site: IM / UN

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

Basal cell carcinoma Biopsy skin abnormal Cancer surgery Peripheral swelling Skin cancer Swelling Swelling face

Symptomtext

In the summertime I did notice a little clear bump on my nose that would come and go. I scheduled an appointment with my dermatologist, and she told me I had skin cancer called basal cell carcinoma. I also had a bump on my back and outer thigh which were also cancerous that I didn't even notice. I had the one on my thigh scraped and burn off, the one on my back I had cut out and stitched up, and the one on my nose I have a surgery scheduled in January.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Basal cell carcinoma
Hospital-Tage: -
Labordaten: Biopsy, 11/09/2022, Basal Cell Carcinoma
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Ibuprofen; TYLENOL; vitamin D
Allergien: Sick when taking narcotics
Vorherige Impfungen: COVID-19 Dose 2, Menstrual Cycle Irregular, Moderna, 04/30/2021

VAERS 2518108

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: WA
Alter: 39,0
Geschlecht: M
Eingang: 28.11.2022
Impfdatum: 27.11.2022
Beginn: 27.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Extra dose administered No adverse event

Symptomtext

The patient was accidently given a COVID Bivalent Booster in addition to the Flucelvax vaccine. The patient had already received the COVID Bivalent Booster on 10/02/2022. When the patient left, they had not experienced any adverse health events (Item #21 should be marked as unknown at this time).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Not sick at time of vaccination
Vorgeschichte: Generalized Anxiety Disorder, Rectal Disease, Spine Disorders
Andere Medikamente: Duloxetine, Omeprazole, Alprazolam
Allergien: Clindamycin, Penicillin
Vorherige Impfungen: -

VAERS 2518061

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: WI
Alter: 17,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 07.11.2022
Beginn: 07.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Patient was given the Pfizer bivalent booster instead of the first of the Pfizer primary series for covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2517872

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: NE
Alter: 27,0
Geschlecht: F
Eingang: 28.11.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

No adverse event reported - patient received bivalent before receiving primary series in error

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None known
Vorgeschichte: None known
Andere Medikamente: alprazolam 0.25 mg
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2517431

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 32,0
Geschlecht: M
Eingang: 27.11.2022
Impfdatum: 25.11.2022
Beginn: 26.11.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

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

Heart rate increased

Symptomtext

Pfizer-BioNTech COVID-19 Vaccine, Bivalent EUA Rapid Heart Beat

Weitere VAERSDATA-Felder

Praegender Schweregrund: Heart rate increased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: ketorolac
Vorherige Impfungen: -

VAERS 2517383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MD
Alter: 65,0
Geschlecht: M
Eingang: 26.11.2022
Impfdatum: 26.11.2022
Beginn: 26.11.2022
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

No Symptoms yet. Patient requested a Pfizer Bivalent Injection. I asked him which number shot, he replied 5th shot. He showed me the front of the card. I gave him the shot and while turning to back of the card I noticed he had already received the bivalent a another pharmacy ..he said he didn't remember

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2517366

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: VT
Alter: 36,0
Geschlecht: F
Eingang: 26.11.2022
Impfdatum: 21.11.2022
Beginn: 21.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Error: Dose in Series 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 2515480

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: WA
Alter: 16,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 23.11.2022
Beginn: 23.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Pt had rec'd Covid-19 Vaccine on 8/04/21 & 8/25/21. She is under 18 years old, therefore should have received monovalent series, rather than a Bivalent booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NO
Vorherige Impfungen: -

VAERS 2515295

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: AZ
Alter: 13,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 23.11.2022
Beginn: 23.11.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / -

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

Incorrect product formulation administered No adverse event Product administration error

Symptomtext

Patient had only received 1 dose in her primary series, was supposed to be getting her 2nd monovalent Pfizer dose. Instead she was given a bivalent Pfizer vaccine. This was an administration error that is required to be reported to VAERS because it is COVID related. No adverse health event occurred.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: none
Andere Medikamente: unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2515251

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: WI
Alter: 8,0
Geschlecht: M
Eingang: 23.11.2022
Impfdatum: 22.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect dose administered Product administered to patient of inappropriate age

Symptomtext

Client was at the COVID-19 clinic on 11-22-22 and was supposed to receive the Pfizer 5-11 bivalent booster, but the nurse accidently gave him the Pfizer 12+ bivalent booster instead. The error was discovered when going through the paperwork/consents. The morning of 11-23-22 the state was contacted regarding the error and we immediately called the mom, to let her know as well. Mom said her son was at school and was feeling fine. We explained that he received a higher dose of the booster and to monitor for increased side effects/ response, but otherwise he should be fine and that it is a valid booster dose. We told her to call with any questions or concerns or to contact her provider. We also explained we would be completing a VAERS report due to the error.

Weitere VAERSDATA-Felder

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

VAERS 2514798

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: CO
Alter: 42,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 20.10.2022
Beginn: -
Tage bis Beginn: -
Dosis: 4
Route/Site: - / RA

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 a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 42-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 20Oct2022 at 15:30 as dose 4 (booster), single (Lot number: GJ3275) at the age of 42 years, in right 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: "Pre-diabetic" (unspecified if ongoing); "prior surgeries like gastric bypass in 2013. No other surgeries have lasting effects.", start date: 2013 (unspecified if ongoing). Concomitant medication(s) included: AMBIEN CR; ZOLPIDEM TARTRATE. Past drug history included: Roxicet, reaction(s): "known allergies: Roxicet". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: COVID 19 Treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical information: Skin sensitivity, bad taste in mouth, those both went away after completing Paxlovid treatment. Was starting to test negative but am now testing positive again. Had a slightly irritated throat. Patient received paxlovid for covid 19 treatment, started on 07Nov2022 and stopped on 12Nov2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: COVID-19 test; Test Result: Positive ; Comments: COVID 19 Treatment
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Gastric bypass; Pre-diabetic
Andere Medikamente: AMBIEN CR; ZOLPIDEM TARTRATE
Allergien: -
Vorherige Impfungen: -

VAERS 2514613

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 11,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 22.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered Product administered to patient of inappropriate age

Symptomtext

PATIENT < 12 YEARS OF AGE RECEIVED THE BIVALENT 3RD SHOT INSTEAD OF MONOVALENT 3RD SHOT

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2514607

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: GA
Alter: 78,0
Geschlecht: M
Eingang: 22.11.2022
Impfdatum: 22.11.2022
Beginn: 01.11.2022
Tage bis Beginn: -
Dosis: 6
Route/Site: IM / LA

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

Extra dose administered

Symptomtext

PATIENT RECIEVED PFIZER BIVALENT BOOSTER IN SEPETERM 9, 2022. PATIENT CAME TO PHARMACY AND REQUESTED A PFIZER BOOSTER, VERIFIED IT HAD BEEN 2 MONTHS SINCE LAST BOOSTER BUT DID NOT VERIFY IF IT WAS MONVALENT OR BIVALENT BOOSTER. PATIENT RECIEVED BOOSTER TODAY 11/22/22. MENTIONED HER RECIEVED A BOOSTER AND SEPETEMBER AND WANTED TO KNOW THE DIFFERENCE. LOOKED AT HIS PROFILE AND REALIZED HE RECIEVED ANOTHER PFIZER BOOSTER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: PLAVIX LISINOPRIL REPATHA NITROGLYCERIN GABAPENTIN
Allergien: STATINS LATEX
Vorherige Impfungen: -

VAERS 2514235

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: GA
Alter: 60,0
Geschlecht: F
Eingang: 22.11.2022
Impfdatum: 22.11.2022
Beginn: 22.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Blood pressure increased

Symptomtext

Patient came in to receive a COVID-19 Booster vaccine. Shortly after receiving the vaccine, pt began to state that her blood pressure was elevated. 911 was called and an ambulance came to evaluate the patient. Patient was found to have an elevated blood pressure of 200/108. Per the clinician vaccinating the patient, she states she has a history of hypertension and takes medication for it. Patient ultimately decided to refuse EMS. Patient signed and AMA form with at Mobile Vax site as well

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood pressure increased
Hospital-Tage: -
Labordaten: Blood Pressure measurement 11/22/2022
Aktuelle Erkrankungen: -
Vorgeschichte: HTN
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2512905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 21.11.2022
Impfdatum: 18.11.2022
Beginn: 20.11.2022
Tage bis Beginn: 2,0
Dosis: 5
Route/Site: IM / LA

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

Burning sensation Erythema Limb discomfort Peripheral swelling

Symptomtext

redness, swelling, burning, little heavyness in arm, but not quite numbness swelling is in all over upper arm (biceps, triceps, deltoid),and underarm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Burning sensation
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2512837

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MI
Alter: 60,0
Geschlecht: M
Eingang: 21.11.2022
Impfdatum: 09.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Product storage error Wrong technique in product usage process

Symptomtext

I administered a bivalent vaccine past the 12+ hours post puncture. although, the dose is considered valid with an excursion time of + 12 hours post puncture.. The standard best practice is to use a vial of Pfizer for 12 hours after puncture I contacted the Health Dept. which I was then directed to call Pfizer mfgr, I was emailed a response that the vial puncture time was 24 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Cardiac and Vasculature Dyslipidemia HTN (hypertension) Coronary artery disease Overview Stent placement December 31, 2012. Endocrine and Metabolic Morbid obesity Impaired fasting glucose Non-insulin dependent diabetes mellitus Gastrointestinal and Abdominal Diverticulosis Overview Diagnosed with colonoscopy 07/03/12 Encounter for colonoscopy due to history of colonic polyp Genitourinary and Reproductive Erectile dysfunction Musculoskeletal and Injuries Osteoarthritis of right hip Overview Has consulted with Dr. regarding hip pain. Dr. has recommended replacement (total hip arthroplasty). Patient is s/p repair of slipped epiphysis as toddler Osteoarthritis of left hip Overview Has consulted with orthopedic surgeon Dr. regarding this. Sleep Obstructive sleep apnea
Vorgeschichte: Cardiac and Vasculature Dyslipidemia HTN (hypertension) Coronary artery disease Overview Stent placement December 31, 2012. Endocrine and Metabolic Morbid obesity Impaired fasting glucose Non-insulin dependent diabetes mellitus Gastrointestinal and Abdominal Diverticulosis Overview Diagnosed with colonoscopy 07/03/12 Encounter for colonoscopy due to history of colonic polyp Genitourinary and Reproductive Erectile dysfunction Musculoskeletal and Injuries Osteoarthritis of right hip Overview Has consulted with Dr. regarding hip pain. Dr. has recommended replacement (total hip arthroplasty). Patient is s/p repair of slipped epiphysis as toddler Osteoarthritis of left hip Overview Has consulted with orthopedic surgeon Dr. regarding this. Sleep Obstructive sleep apnea
Andere Medikamente: aspirin 325 MG tablet blood sugar test strips dapagliflozin (Farxiga) 10 mg tablet fluticasone propionate (FLONASE ALLERGY RELIEF NASL) lancets (COMFORT LANCETS) Misc lisinopriL-hydrochlorothiazide (Zestoretic) 20-12.5 mg per tablet metFORM
Allergien: N/A
Vorherige Impfungen: -

VAERS 2510922

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: CO
Alter: 7,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 10.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Pt received the Pfizer monovalent instead of Pfizer Bivalent for the booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2510797

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 63,0
Geschlecht: M
Eingang: 17.11.2022
Impfdatum: 17.11.2022
Beginn: 17.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Member was suppose to receive first dose of Pfizer and member was given in error Pfizer bivalent. Dr. was notified. Per Dr. adverse member is to come back in 2 weeks and receive one dose of Pfizer mono. Member was advised to stay at clinic for 30 minutes and be monitored for any adverse reactions. Member stayed the 30 minutes. Member verbalized feeling well. Member left clinic after 30 minutes.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: None. Member was observed at clinic by staff for 30 minutes,
Aktuelle Erkrankungen: CAD Heart Failure W Reduced LVEF <=30%, Unspecified Aucity HTN Major Depressive Disorder, Recurrent Episodes Elevated Troponin 1 HX of Covid -19 Disease HX of Embolic Stroke Nontraumatic Acute Kidney Injury Obesity BMI 30-34.9 Adult Hypertensive Retinopathy Systolic Heart Failure, Acute
Vorgeschichte: CAD Heart Failure W Reduced LVEF <=30%, Unspecified Aucity HTN Major Depressive Disorder, Recurrent Episodes Elevated Troponin 1 HX of Covid -19 Disease HX of Embolic Stroke Nontraumatic Acute Kidney Injury Obesity BMI 30-34.9 Adult Hypertensive Retinopathy Systolic Heart Failure, Acute
Andere Medikamente: Lasix Coreg Cozaar 25mg Lipitor 40mg Pepcid 20mg Jardiance 25mg Aspirin 81mg
Allergien: No Know Allergies
Vorherige Impfungen: -

VAERS 2510771

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: NC
Alter: 67,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 17.11.2022
Beginn: 17.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Asthenia Impaired driving ability

Symptomtext

Patient felt weak and not able to drive home. EMS was called and patient was taken to hospital for further evaluation.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, kidney disease, liver disease
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2510462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: OR
Alter: 55,0
Geschlecht: F
Eingang: 17.11.2022
Impfdatum: 13.11.2022
Beginn: 13.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2509945

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MA
Alter: 9,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 07.11.2022
Beginn: 07.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / LA

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

Incorrect dose administered

Symptomtext

PATIENT RECEIVED PFIZER BI-VALENT ADULT DOSE. PATIENT IS 9 YEARS OLD

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 2509748

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: IN
Alter: 85,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 11.11.2022
Beginn: 11.11.2022
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / RA

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

Inappropriate schedule of product administration

Symptomtext

Patient received Pfizer Bivalent vaccine on 9/14/22 and 11/11/22. No symptoms noted at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension, Hypothyroid, Diabetes, Hypercholesterolemia, Squamous cell carcinoma, Chronic embolism and thrombosis of deep vein lower extremity, Osteoarthritis, Insomnia, Dementia
Andere Medikamente: Aspirin, Atorvastatin, Vitamin D, Latanoprost, Furosemide, Levothyroxine, Calcium, Trazodone, Melatonin, Acetaminophen , Seroquel, Zoloft, Novolog, Basaglar
Allergien: NKA
Vorherige Impfungen: -

VAERS 2509311

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: CA
Alter: 40,0
Geschlecht: F
Eingang: 16.11.2022
Impfdatum: 08.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Product storage error

Symptomtext

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2509310

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: CA
Alter: 63,0
Geschlecht: M
Eingang: 16.11.2022
Impfdatum: 08.11.2022
Beginn: 08.11.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Product storage error

Symptomtext

Error: Improper Storage (ex. temp./location)-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2508930

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: FL
Alter: 10,0
Geschlecht: F
Eingang: 15.11.2022
Impfdatum: 15.11.2022
Beginn: 15.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect dose administered No adverse event

Symptomtext

Patient should have received Pfizer for 5-11 year old 0.2ml but received adult pfizer 12+ 0.3ml , Mother reported no adverse effects at this time.

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 2507944

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: NJ
Alter: -
Geschlecht: M
Eingang: 15.11.2022
Impfdatum: 28.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: - / RA

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

Vertigo

Symptomtext

woke up with short mild vertigo like symptoms; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 62-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Oct2022 at 10:00 as dose 5 (booster), single (Lot number: GJ3275), in right arm for covid-19 immunisation. The patient's relevant medical history included: "pulmonary embolism" (unspecified if ongoing); "factor V leiden" (unspecified if ongoing), notes: Other medical history: factor V leiden; "type II diabetes" (unspecified if ongoing), notes: Other medical history: type II diabetes; "morbid obesity" (unspecified if ongoing); "bilateral lymphedema legs" (unspecified if ongoing). Concomitant medication(s) included: WARFARIN SODIUM; ALLOPURINOL; CRESTOR; LASIX [FUROSEMIDE SODIUM]. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot number: PHIZEREW0162, Anatomical location:, Arm Right, Vaccine Administration Time: 09:00 AM), administration date: 11Mar2021, when the patient was 60-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE, Lot number: PHIZERER8727, Anatomical location:, Arm Right, Vaccine Administration Time: 09:00 AM), administration date: 21Mar2021, when the patient was 60-year-old, for COVID-19 immunization, reaction(s): "Dose 1: 11Mar2021; Dose 2: 21Mar2021"; BNT162b2 (DOSE 3 (BOOSTER), SINGLE, Lot number: PHIZERFH8027, Anatomical location: Arm Right, Vaccine Administration Time: 10:00 AM), administration date: 19Oct2021, when the patient was 61-year-old, for COVID-19 immunization; BNT162b2 (DOSE 4 (BOOSTER), SINGLE, Lot number: PHIZERFK9893, Anatomical location: Arm Right, Vaccine Administration Time: 10:00 AM), administration date: 22Apr2022, when the patient was 61-year-old, for COVID-19 immunization. The following information was reported: VERTIGO (non-serious) with onset 29Oct2022 at 07:00, outcome "not recovered", described as "woke up with short mild vertigo like symptoms". Therapeutic measures were not taken as a result of vertigo. Additional information: The patient had no known allergies. Prior to vaccination, the patient was not diagnosed with COVID. The patient did not receive other vaccine in four weeks. Post vaccination, the patient was not tested for COVID.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vertigo
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Factor V Leiden carrier (Other medical history: factor V leiden); Lymphedema; Morbid obesity; Pulmonary embolism; Type II diabetes mellitus (Other medical history: type II diabetes)
Andere Medikamente: WARFARIN SODIUM; ALLOPURINOL; CRESTOR; LASIX [FUROSEMIDE SODIUM]
Allergien: -
Vorherige Impfungen: -

VAERS 2507514

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: CO
Alter: 19,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 10.11.2022
Beginn: 10.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

No adverse event Wrong product administered

Symptomtext

pt was given the Omicron booster instead of the 1st does of the Pfizer series. No side effects at time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2507358

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: WI
Alter: 10,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 14.11.2022
Beginn: 14.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Product administered to patient of inappropriate age

Symptomtext

The patient received adult dose of COVID booster, instead of 5-11 yr. olds.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2507180

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 12.11.2022
Beginn: 13.11.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Contusion Erythema Mass

Symptomtext

egg like lump and a 2 inch red band underneath also black and blue

Weitere VAERSDATA-Felder

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

VAERS 2506452

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: IL
Alter: 78,0
Geschlecht: F
Eingang: 11.11.2022
Impfdatum: 08.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 1,0
Dosis: 5
Route/Site: IM / LA

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

Neurological symptom

Symptomtext

Patient demonstrated stroke-like symptoms and was taken to the hospital by ambulance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Neurological symptom
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Cevimeline, Hydroxychloroquine, Levothyroxine
Allergien: NKA
Vorherige Impfungen: -

VAERS 2499566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MA
Alter: 7,0
Geschlecht: M
Eingang: 11.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered No adverse event Product administered to patient of inappropriate age

Symptomtext

Patient is 7 years old, but was administered an an adult dose of the Pfizer Covid booster. This was a pharmacist error. He has ad no adverse reaction thus far (it's been a week now). However, we are concerned about any potential long term effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Microtia and hearing loss
Andere Medikamente: Daily multivitamin, probiotic, DHA supplement
Allergien: N/A
Vorherige Impfungen: -

VAERS 2499566

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MA
Alter: 7,0
Geschlecht: M
Eingang: 11.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Incorrect dose administered No adverse event Product administered to patient of inappropriate age

Symptomtext

Patient is 7 years old, but was administered an an adult dose of the Pfizer Covid booster. This was a pharmacist error. He has ad no adverse reaction thus far (it's been a week now). However, we are concerned about any potential long term effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Microtia and hearing loss
Andere Medikamente: Daily multivitamin, probiotic, DHA supplement
Allergien: N/A
Vorherige Impfungen: -

VAERS 2504414

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: IN
Alter: 38,0
Geschlecht: F
Eingang: 10.11.2022
Impfdatum: 09.11.2022
Beginn: 09.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Patient received 1.8mL of the vaccine equaling a total of 6 doses when patient should have received 0.3mL equaling one dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None noted
Vorgeschichte: Cervical stenosis (uterine cervix), genital herpes simplex
Andere Medikamente: Adderall XR, atorvastatin, docusate sodium
Allergien: Penicillins
Vorherige Impfungen: -

VAERS 2504352

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 5,0
Geschlecht: M
Eingang: 10.11.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Patient was scheduled to receive a Primary Pediatric Pfizer 5yrs-11yrs 2nd dose, but was mistakenly given a Pediatric Pifzer Bivalent dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2507055

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: -
Alter: 72,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 19.10.2022
Beginn: 19.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt 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 2502013

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: WI
Alter: 77,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 07.11.2022
Beginn: 07.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Pfizer Bivalent booster vaccine was administered as the 1 dose in the Primary Series instead of the monovalent Comirnaty. Patient was informed. Per CDC recommendations, dose was not repeated and patient is scheduled to return in 21 days for the monovalent pfizer 2nd dose. No adverse effects noted.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2501975

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: WI
Alter: 10,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 27.10.2022
Beginn: 30.10.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect product formulation administered Product administered to patient of inappropriate age

Symptomtext

given bivalent not pediatric vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2501971

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MI
Alter: 37,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 26.10.2022
Beginn: 01.11.2022
Tage bis Beginn: 6,0
Dosis: 4
Route/Site: IM / AR

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

Angiogram abnormal Imaging procedure abnormal Retinal ischaemia Retinal vein occlusion Vision blurred Visual impairment

Symptomtext

Blurry vision and a dimness OS in the upper portion of her vision; Patches of lightness/darkness OS. Branch Retinal Vein Occlusion OS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Angiogram abnormal
Hospital-Tage: -
Labordaten: exam and imaging consistent with BRVO; Fluoroscein angiogram shows peripheral nonperfusion but no neovascularization;
Aktuelle Erkrankungen: Factor V Leiden mutation/deficiency; Fibromyalgia; asthma; RLS; ADHD; TMJ; Depression
Vorgeschichte: Factor V Leiden mutation/deficiency; Fibromyalgia; asthma; RLS; ADHD; TMJ; Depression
Andere Medikamente: Horse chestnut 167mg; Iron 50mg; Imiquimod 5% creme (feet/hand); albuterol inhaler; Eliquis 5mg; Betamethadone 0.05% lotion (scalp); wellbutrin xl 300mg; vitamin D 5000u; Adderall 25mg; ketoconazole 2% shampoo; claritin 10mg; nystatin ointm
Allergien: -
Vorherige Impfungen: -

VAERS 2501918

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MI
Alter: 8,0
Geschlecht: M
Eingang: 08.11.2022
Impfdatum: 05.11.2022
Beginn: 05.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Incorrect dose administered

Symptomtext

Pt was given 0.5mL instead of 0.25mL

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2500905

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 23,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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 2500665

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: AZ
Alter: 58,0
Geschlecht: M
Eingang: 07.11.2022
Impfdatum: 06.11.2022
Beginn: 06.11.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Hyperhidrosis Pallor

Symptomtext

after receiving vaccines( shingrix, flushot, and pfizer bivalent booster), patient exhibited the following symptoms in the waiting room;sweating and getting pale. manual blood pressure was around 70/40 and I gave patient water. 911 was called. After about 10 minutes of drinking fluid patient's pressure started to go back up. blood pressure went to 130/80 and blood sugar was 130 was checked by paramedic. patient was stable and was offered to go the ER but refused. patient was picked up by family member

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hyperhidrosis
Hospital-Tage: -
Labordaten: first blood pressure 70/40 second blood pressure 130/80 (after drink fluid)
Aktuelle Erkrankungen: N/A
Vorgeschichte: HIGH BLOOD PRESSURE, DIABETES
Andere Medikamente: N/A
Allergien: NKA
Vorherige Impfungen: -

VAERS 2500603

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: IL
Alter: 30,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 07.11.2022
Beginn: 07.11.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Patient was in the office for second primary series of Pfizer vaccine but was given bivalent booster instead.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: No known
Vorherige Impfungen: -

VAERS 2500542

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: GA
Alter: 11,0
Geschlecht: F
Eingang: 07.11.2022
Impfdatum: 29.10.2022
Beginn: 29.10.2022
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 Product administered to patient of inappropriate age

Symptomtext

Patient was 11 years and 9 months old when she received the Covid Pfizer Bivalent , gray cap, for ages 12 and up. No immediate adverse outcomes noted. Team Supervisor left voicemail notifying parent and requesting follow up phone call. No return call by parent. Attempted to reach out again via phone but no return call by parent. Parent did not leave any email address on consent form.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: unknown
Andere Medikamente: n/a
Allergien: none
Vorherige Impfungen: -

VAERS 2500035

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 18,0
Geschlecht: M
Eingang: 06.11.2022
Impfdatum: 22.10.2022
Beginn: 22.10.2022
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

Error: Dose in Series 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 2499929

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: NC
Alter: 19,0
Geschlecht: F
Eingang: 05.11.2022
Impfdatum: 01.11.2022
Beginn: 01.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Patient stated she wanted to receive her first COVID vaccine. This was missed by the pharmacist on duty and the vaccine was processed as a second booster. Patient was administered Bivalent Pfizer dose as her first dose when she had never received any COVID vaccine prior to the event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Sprintec
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2499570

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MA
Alter: 8,0
Geschlecht: M
Eingang: 04.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered No adverse event Product administered to patient of inappropriate age

Symptomtext

Pharmacist was reviewing vaccines given earlier in the day when she noticed the pediatric bivalent booster was not opened but kids under the age of 12 came in earlier in the day. The pharmacist asked the pharmacy intern that was administering vaccines and she realized that she gave the wrong dose to the child (an adult pfizer booster was given instead of pediatric). Patient was asked to monitor for symptoms and the doctor was reached out to. They do not see any major side effects occurring for the patient. No adverse event reported for the patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2499556

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge GJ3275

gering

Staat: NY
Alter: 11,0
Geschlecht: F
Eingang: 04.11.2022
Impfdatum: 04.11.2022
Beginn: 04.11.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

No adverse event Product administered to patient of inappropriate age

Symptomtext

The client was given a Pfizer 12 year and up vaccine instead of Pedi Pfizer 5-11 years old. No adverse symptoms. Mom made aware: the child was still in clinic waiting the 15 minutes after the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: 2 doses of Pedi Pfizer

VAERS 2498229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 03.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Drooling Lip swelling Oropharyngeal discomfort Salivary hypersecretion Throat tightness

Symptomtext

Patient stated she felt her throat tighten and was oversalivating after receiving the bivalent booster, after 30 minute observation period.

Weitere VAERSDATA-Felder

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

VAERS 2498229

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: CA
Alter: 68,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 03.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / OT

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

Drooling Lip swelling Oropharyngeal discomfort Salivary hypersecretion Throat tightness

Symptomtext

Patient stated she felt her throat tighten and was oversalivating after receiving the bivalent booster, after 30 minute observation period.

Weitere VAERSDATA-Felder

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

VAERS 2497888

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 11,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 02.11.2022
Beginn: 02.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect product formulation administered Product administered to patient of inappropriate age

Symptomtext

Administered vaccine that is only authorized for 12 and older to a 11 year old. No adverse effects occurred. Patient's parents were notified as well as the physician. Pfizer Bivalent administered instead of Moderna Bivalent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Unknown
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2497835

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: FL
Alter: 27,0
Geschlecht: M
Eingang: 03.11.2022
Impfdatum: 03.11.2022
Beginn: 03.11.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

No adverse event Wrong product administered

Symptomtext

No adverse reaction observed. Miscommunication at check-in and screening. Pt received Bivalent booster as Primary dose 1.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2495371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: TN
Alter: 35,0
Geschlecht: M
Eingang: 01.11.2022
Impfdatum: 25.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Inadvertantly given Pfizer bivalent as 1st dose primary series. Will return in 21 days for 2nd dose of Pfizer monovalent.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: no history reported
Andere Medikamente: none
Allergien: nka
Vorherige Impfungen: -

VAERS 2495259

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: IL
Alter: 46,0
Geschlecht: F
Eingang: 01.11.2022
Impfdatum: 01.11.2022
Beginn: 01.11.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Unevaluable event

Symptomtext

Patient recovered and was able to go home with vital signs and respirations with in normal limits.e

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: Diabetes, HTN, CAD, Migraine, Bi Polar
Vorgeschichte: -
Andere Medikamente: atorvastatin (LIPITOR) 40 MG Tablet cholestyramine (QUESTRAN) 4 GM Pack Empagliflozin (JARDIANCE) 10 MG Tablet Glucose Blood Strip Insulin Pen Needle (Easy Touch Pen Needles) 32G X 5 MM Misc Insulin Pen Needle (NovoFine) 32G X 6 MM Misc Lan
Allergien: Dilaudid [Hydromorphone] Unknown Not Specified Allergy 11/6/2018 Past Updates... Gabapentin Unknown Not Specified Allergy 11/6/2018 Past Updates... Norco [Hydrocodone-acetaminophen] Unknown Not Specified Allergy 11/6/2018 Past Updates... Pineapple
Vorherige Impfungen: -

VAERS 2493425

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: AZ
Alter: 32,0
Geschlecht: F
Eingang: 29.10.2022
Impfdatum: 29.10.2022
Beginn: 29.10.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Extra dose administered Incorrect product formulation administered

Symptomtext

Patient already received flu vaccine on 10/06/22. Patient was also on 2nd dose of covid, but received pfizer bivalent (booster).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: liver disease
Andere Medikamente: no
Allergien: no
Vorherige Impfungen: -

VAERS 2492728

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MN
Alter: 9,0
Geschlecht: M
Eingang: 28.10.2022
Impfdatum: 18.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect dose administered Product administered to patient of inappropriate age

Symptomtext

SON was given 12+ Pfizer Bivalent Shot (gray cap) when it was supposed to be pediatrics dose (orange cap)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2492718

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MN
Alter: 9,0
Geschlecht: M
Eingang: 28.10.2022
Impfdatum: 18.10.2022
Beginn: 18.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / -

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

Product administered to patient of inappropriate age Wrong product administered

Symptomtext

Daughter was given 12+ Pfizer Bivalent Shot (gray cap) when it was supposed to be pediatrics dose (orange cap)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2492697

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: MN
Alter: 9,0
Geschlecht: F
Eingang: 28.10.2022
Impfdatum: 19.10.2022
Beginn: 19.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered

Symptomtext

Daughter was given 12+ Pfizer Bivalent Shot (gray cap) when it was supposed to be pediatrics dose (orange cap)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2492462

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: IN
Alter: 20,0
Geschlecht: M
Eingang: 28.10.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Incorrect dose administered No adverse event

Symptomtext

Patient was given Bivalent dose instead of second dose of primary series. No treatment or side effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: lexapro atarax
Allergien: NKA
Vorherige Impfungen: -

VAERS 2492044

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 75,0
Geschlecht: M
Eingang: 27.10.2022
Impfdatum: 27.10.2022
Beginn: 27.10.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event Wrong product administered

Symptomtext

Nurse administered COVID PFIZER BIVALENT BOOSTER, when patient was due for COVID PFIZER SECOND DOSE PRIMARY SERIES. Nurse did not pay attention when reading the printed immunization record that patient had only received one dose of Pfizer. Patient was called and notified that he received the wrong vaccine. Patient stated that he did not have any symptoms and they will come back in 2 months for their booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Chemo/Immunosuppressive or other Infusion Treatment
Allergien: -
Vorherige Impfungen: -

VAERS 2491280

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: GA
Alter: 70,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 26.10.2022
Beginn: 26.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: SYR / LA

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

Inappropriate schedule of product administration

Symptomtext

Patient received a pfizer covid-19 bivalent booster on 09/12/2022 and the patient was vaccinated again on 10/26/2022 with another pfizer covid-19 bivalent booster on 10/26/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2490946

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge gj3275

gering

Staat: CA
Alter: 41,0
Geschlecht: F
Eingang: 27.10.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Error: Wrong Vaccine/Product Administered-

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2490408

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 12,0
Geschlecht: M
Eingang: 26.10.2022
Impfdatum: 24.10.2022
Beginn: 24.10.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Nurse administered Pfizer Bivalent Booster when patient was due for Pfizer Second Dose in primary series. Parents were made aware of incident. Patient is scheduled to talk to a provider.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2488869

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: WI
Alter: 9,0
Geschlecht: M
Eingang: 25.10.2022
Impfdatum: 25.10.2022
Beginn: 25.10.2022
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: IM / RA

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

Incorrect product formulation administered Product administered to patient of inappropriate age

Symptomtext

BiValent vaccine for age 12+ given to patient age 9 years

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2488193

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: -
Alter: 50,0
Geschlecht: M
Eingang: 25.10.2022
Impfdatum: 20.10.2022
Beginn: 20.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / RA

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

Inappropriate schedule of product administration

Symptomtext

Patient received Pfizer Bivalent Booster in clinic on 9/26/22 and then again on 10/20/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Erythromycin
Vorherige Impfungen: -

VAERS 2486572

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 23.10.2022
Impfdatum: 22.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Interchange of vaccine products No adverse event

Symptomtext

Patient requested Moderna bivalent vaccine but received Pfizer bivalent vaccine. No adverse events reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2486569

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge gj3275

gering

Staat: -
Alter: 90,0
Geschlecht: F
Eingang: 23.10.2022
Impfdatum: 22.10.2022
Beginn: 22.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

No adverse event Wrong product administered

Symptomtext

Patient had requested the Moderna bivalent vaccine but was given Pfizer bivalent vaccine. No adverse events reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2486495

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: -
Alter: 16,0
Geschlecht: M
Eingang: 23.10.2022
Impfdatum: 30.09.2022
Beginn: 30.09.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Pfizer bivalent booster given as first dose of primary series

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2485823

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: AZ
Alter: 16,0
Geschlecht: F
Eingang: 21.10.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Extra dose administered

Symptomtext

I accidently gave pt an extra dose of pfizer new bivalent booster shot on 10/21/22 Today. Pt received it on 9/13/2022. There is no harm caused. I informed pt's mom of this incident and explained to her that this is not harmful but unnecessary and she can call if she can have any question.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: None
Vorgeschichte: Major depressive disorder, Generalized anxiety disorder,
Andere Medikamente: None
Allergien: No Known Allergies
Vorherige Impfungen: -

VAERS 2485808

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: TX
Alter: 38,0
Geschlecht: M
Eingang: 21.10.2022
Impfdatum: 21.10.2022
Beginn: 21.10.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

PATIENT HAD NOT COMPLETED A PRIMARY SERIES AND WAS GIVEN PFIZER BIVALENT AS HIS SECOND DOSE. PATIENT HAD ONLY RECEIVED 1 PFIZER DOSE PREVIOUSLY.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2485556

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: IL
Alter: 20,0
Geschlecht: M
Eingang: 21.10.2022
Impfdatum: 17.10.2022
Beginn: 17.10.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

No adverse event

Symptomtext

There were no side effects reported from pt.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: No testing was needed.
Aktuelle Erkrankungen: No Acute Illness
Vorgeschichte: Neurologic Epileptic seizures Generalized convulsive epilepsy without intractable epilepsy Abnormal brain MRI Behavioral / Psychiatric Autistic disorder of childhood onset Oppositional defiant behavior
Andere Medikamente: Dicyclomine Omeprazole
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2481647

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

gering

Staat: CA
Alter: 33,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient was given a Pfizer Bivalent booster dose instead of a first dose of Primary Pfizer by Registered Nurse. No adverse reaction was noted,

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2481597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 39,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer due to medication administration error. Pfizer monovalent/bivalent vials look similar and have the same-colored caps which led to the pharmacist drawing up the wrong dose. Patient was informed of the error within a few days and provided medical advice. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Not on file
Vorgeschichte: Not on file
Andere Medikamente: Not on file
Allergien: Not on file
Vorherige Impfungen: -

VAERS 2481595

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 44,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 6
Route/Site: IM / RA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer due to medication administration error. Pfizer monovalent/bivalent vials look similar and have the same-colored caps which led to the pharmacist drawing up the wrong dose. Patient was informed of the error within a few days and provided medical advice. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HIV, AIDS, Anal condyloma, corneal ectasia of both eyes, allergic conjunctivitis of both eyes, glaucoma
Andere Medikamente: acetaminophen 500 mg oral tablet, bictegravir-emtricitabine-tenofovir 50-200-25 mg oral tablet, latanoprost 0.005% ophthalmic, sodium chloride 0.9% inhalation solution for nebuilization, trimethorprim-sulfamethoxazole 80-400 mg oral tablet
Allergien: Naproxen
Vorherige Impfungen: -

VAERS 2481591

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 37,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer due to medication administration error. Pfizer monovalent/bivalent vials look similar and have the same-colored caps which led to the pharmacist drawing up the wrong dose. Patient was informed of the error within a few days and provided medical advice. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Not on file
Vorgeschichte: Not on file
Andere Medikamente: Not on file
Allergien: Not on file
Vorherige Impfungen: -

VAERS 2481590

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 44,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Incorrect dose administered Product administration error Wrong product administered

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer due to medication administration error. Pfizer monovalent/bivalent vials look similar and have the same-colored caps which led to the pharmacist drawing up the wrong dose. Patient was informed of the error within a few days and provided medical advice. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481589

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 65,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer due to medication administration error. Pfizer monovalent/bivalent vials look similar and have the same-colored caps which led to the pharmacist drawing up the wrong dose. Patient was informed of the error within a few days and provided medical advice. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: alendronate, 70 mg oral tablet, amLODIPine, 5 mg oral tablet, ATORVASTATIN 10 mg oral tablet, elvitegravir-cobicistat-emtricitabine-tenofavir ala, losartan 25 mg oral tablet, omeprazole 20 mg oral capsule
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481586

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 36,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect dose administered Product administration error Wrong product administered

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer due to medication administration error. Pfizer monovalent/bivalent vials look similar and have the same-colored caps which led to the pharmacist drawing up the wrong dose. Patient was informed of the error within a few days and provided medical advice. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481583

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 42,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Incorrect dose administered No adverse event Product administration error Wrong product administered

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer due to medication administration error. Pfizer monovalent/bivalent vials look similar and have the same-colored caps which led to the pharmacist drawing up the wrong dose. Patient was informed of the error within a few days and provided medical advice. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481383

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 28,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer due to medication administration error. Pfizer monovalent/bivalent vials look similar and have the same-colored caps which led to the pharmacist drawing up the wrong dose. Patient was informed of the error within a few days and provided medical advice. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481378

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 27,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer due to medication administration error. Pfizer monovalent/bivalent vials look similar and have the same-colored caps which led to the pharmacist drawing up the wrong dose. Patient was informed of the error within a few days and provided medical advice. No adverse reactions reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481375

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 61,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer vaccine instead of intended 0.3 mL bivalent Pfizer booster. Medication administration error due to Pfizer monovalent/bivalent vials looking similar with same-colored caps.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481371

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 54,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer booster. No adverse reaction occurred; medication administration error due to Pfizer monovalent/bivalent vials looking similar.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481369

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 54,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer vaccine instead of intended 0.3 mL bivalent Pfizer booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481174

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 38,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481173

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 32,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

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

Incorrect product formulation administered

Symptomtext

patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481172

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 33,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Wrong product administered

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481171

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 46,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481170

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 47,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer instead of intended 0.3 mL bivalent Pfizer booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481169

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

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Staat: OR
Alter: 70,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SC / AR

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

Wrong product administered

Symptomtext

Patient was administered 0.3 mL monovalent Pfizer vaccine instead of intended 0.3 mL bivalent Pfizer booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Wrong product administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2481167

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

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Staat: OR
Alter: 39,0
Geschlecht: M
Eingang: 18.10.2022
Impfdatum: 01.03.1983
Beginn: 09.10.2022
Tage bis Beginn: 14.467,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered

Symptomtext

Patient was administered a 0.3 mL dose of monovalent Pfizer vaccine instead of intended 0.3 mL bivalent Pfizer vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: none known
Allergien: none known
Vorherige Impfungen: -

VAERS 2479611

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

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Staat: CT
Alter: 72,0
Geschlecht: M
Eingang: 15.10.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / RA

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

Blood glucose increased

Symptomtext

I am diabetic. My wife and I both got the Pfizer omicron booster vaccine on 10/14/2022 at around 9:30 AM. I have a FreeStyle Libre 2 CGM. About 2 hours after getting the vaccine my meter gave me a high glucose warning. I had my normal breakfast food and my normal AM Novolog dosage. My glucose reading spiked at 380 which is extremely high for me since my diabetes has been under control for many years. I gave myself a larger than normal Novolog dose after seeing the glucose spike, I had lunch and glucose numbers lowered but were still around 270. My only explaination is that the glucose spike was due to the vaccine. I looked it up on internet and found one article saying that the vaccine could spike glucose levels briefly. I didn't have a glucose spike (side effect) with any other vaccines (Pfizer?s covid 1, 2, and 1st booster, senior hi-dose flu vaccine, and shingles vaccine). After a few Novolog injections, my glucose became more normal measuring 150 after supper, but still higher than normal today. I think there should have been more Covid omicron booster vaccine warnings for diabetics. If someone had high glucose numbers to begin with before the vaccine, this could put them in the hospital, specially if they did not have the CGM warning. I'll relate this to my doctor on next visit. BTW: My niece who is diabetic had a similar effect with the Moderna omicron booster, her numbers went back to normal the next day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Blood glucose increased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: diabetes
Vorgeschichte: Diabetes
Andere Medikamente: Novolog and Basaglar insulin, lovastatin, losinipril, low dose aspirin
Allergien: no allergies
Vorherige Impfungen: -

VAERS 2478898

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge GJ3275

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Staat: WI
Alter: 13,0
Geschlecht: F
Eingang: 14.10.2022
Impfdatum: 14.10.2022
Beginn: 14.10.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

No adverse events, but patient was due for pfizer #2 monovalent and I ordered the bivalent booster, which was given instead, so reporting per CDC recommendations

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2473347

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

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Staat: WA
Alter: 52,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Pharmacist drew up 0.3 mL of Pfizer monovalent vaccine and vaccinator administered instead of the intended 0.3 mL Pfizer bivalent vaccine. No adverse reactions or symptoms were observed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None known
Vorgeschichte: None known
Andere Medikamente: None known
Allergien: None known
Vorherige Impfungen: -

VAERS 2473335

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

gering

Staat: OR
Alter: 48,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient was administered a dose of Pfizer 0.3 mL monovalent instead of the Pfizer 0.3 mL bivalent vaccine. Pharmacist drew up the wrong vaccine type. No adverse reaction from patient was observed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None known
Vorgeschichte: None known
Andere Medikamente: None known
Allergien: None known
Vorherige Impfungen: -

VAERS 2473314

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge GJ3275

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Staat: OR
Alter: 40,0
Geschlecht: M
Eingang: 10.10.2022
Impfdatum: 09.10.2022
Beginn: 09.10.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / LA

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

Incorrect product formulation administered No adverse event

Symptomtext

Patient was supposed to be administered a dose of Pfizer 0.3 mL bivalent and pharmacist drew up Pfizer 0.3 mL monovalent vaccine. No symptoms or adverse reactions known.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect product formulation administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None on file
Vorgeschichte: None on file
Andere Medikamente: None on file
Allergien: None on file
Vorherige Impfungen: -