- Staat
- -
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 29.12.2023
- Impfdatum
- 16.11.2022
- Beginn
- 18.11.2023
- Tage bis Beginn
- 367,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute myocardial infarction
Acute respiratory failure
Atrial fibrillation
Blood creatinine increased
Chronic kidney disease
Chronic obstructive pulmonary disease
Condition aggravated
Cough
Diuretic therapy
COVID-19
Cardiac failure acute
Cardiac failure congestive
Cardiomegaly
Chest X-ray abnormal
Dyspnoea
Ejection fraction decreased
Fatigue
Symptomtext
Patient is a 83 y.o. male patient of DO with history of CHF and COPD who presented with a 3-day complaint of SOB, subjective fever, dry cough and fatigue. His wife was admitted to the hospital 2 days prior with COVID-19 infection. Patient tested positive for COVID-19. CXR showed stable cardiomegaly with no acute pulmonary disease. He was admitted for further evaluation and management of shortness of breath. Acute on chronic systolic CHF Limited 2D echo on 11/20 Showed global hypokinesis of LV, EF of 34%. RV is enlarged. Noted elevated proBNP 2194 -> 1822 Exacerbation likely triggered by acute infection. He was diuresed and held due to hypotension. Appreciate cardiology input. Continue medical management as permitted by BP. Elevated troponin Troponin I was 99-95-85. Likely type II MI event from acute systolic dysfunction. Troponin essentially flat. Denies chest pain. Continue to monitor. Chronic A. Fib HR is controlled. Continue Coreg. INR 2.3. Pharmacy assisting with warfarin adjustments. Covid-19 Virus Infection COPD Date of onset of symptoms: 11/15 Symptoms present on admission: Cough and SOB Date of covid positive test: 11/18 Vaccination status: unvaccinated Imaging: CXR with no acute infiltrates. Oxygen requirements on admission: Room air Current oxygen requirements: Room air Medical therapy: Bronchodilators. Consultants following: ID Anticipated special isolation end date: 11/26 Worsening oxygenation requiring 2 L NC but now on room air 96% Pox. Appreciate ID input, on remdesivir, monitor renal function. Wean Solu-Medrol. Acute respiratory failure Due to COVID-19. Improved. Continue bronchodilators. Add scheduled Albuterol MDI. Wean O2 as able to. Albuterol MDI scheduled. Diabetes mellitus II Last HbA1c was 7.7 in May 2023. At home he was on Humulin 70/30, Lantus and Humalog. Discussed with endocrinology, insulin adjustments will be made. AKI on CKD III Cr 2.26 -> 1.76. He is nonoliguric. Avoid nephrotoxins. Monitor Cr while on diuretics.. BLE stasis dermatitis No sign of acute infection. Continue to monitor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 15.11.2023
- Impfdatum
- 16.11.2022
- Beginn
- 05.10.2023
- Tage bis Beginn
- 323,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Blood culture negative
COVID-19
Chest X-ray normal
Chronic obstructive pulmonary disease
Condition aggravated
Diabetes mellitus inadequate control
Dyspnoea
Glycosylated haemoglobin
Insulin therapy
Leukocytosis
SARS-CoV-2 test positive
White blood cell count increased
Symptomtext
Patient is a 58 y.o. female patient of DO with history of COPD, hypertension, hyperlipidemia, hypothyroidism, diabetes presented to Hospital with shortness of breath. COPD with acute exacerbation Acute hypoxemic respiratory failure Started on Solu-Medrol 40 every 8 IV, will discontinue and transition to IV Dexamethasone - course completed IV Rocephin stopped 10/8/23- discharge home on Azithromycin 500 mg oral daily x 5 days Albuterol inhaler Discontinue IV fluids Pain management Blood cultures negative Sputum culture- not collected Wean Oxygen as tolerated- currently 98% on room air Leukocytosis- chronic Likely reactive to steroids WBC- 23.2->16.02>18.82>20.42 Afebrile Covid-19 Virus Infection Date of onset of symptoms: 10/3/2023 Symptoms present on admission: Yes Date of covid positive test: 10/5/2023 Vaccination status: vaccinated 1 dose Imaging: Chest x-ray unremarkable Oxygen requirements on admission: 2 L Current oxygen requirements: room air Medical therapy: steroids Remdesivir Consultants following: ID Anticipated special isolation end date: 10/15/2023 Encourage prone position as tolerated DISCHARGE SUMMARY Admitted: 10/5/2023 Discharge Date: 10/12/23 PCP Handoff Recommended Outpatient Testing: none Results Pending At Discharge: none Clinical Summary Patient is a 58 y.o. female patient of DO with history of COPD, hypertension, hyperlipidemia, hypothyroidism, diabetes presented to Hospital with shortness of breath. COPD with acute exacerbation Acute hypoxemic respiratory failure Started on Solu-Medrol 40 every 8 IV, will discontinue and transition to IV Dexamethasone - course completed IV Rocephin stopped 10/8/23- discharge home on Azithromycin 500 mg oral daily x 5 days Albuterol inhaler Discontinue IV fluids Pain management Blood cultures negative Sputum culture- not collected Wean Oxygen as tolerated- currently 98% on room air Leukocytosis- chronic Likely reactive to steroids WBC- 23.2->16.02>18.82>20.42 Afebrile Covid-19 Virus Infection Date of onset of symptoms: 10/3/2023 Symptoms present on admission: Yes Date of covid positive test: 10/5/2023 Vaccination status: vaccinated 1 dose Imaging: Chest x-ray unremarkable Oxygen requirements on admission: 2 L Current oxygen requirements: room air Medical therapy: steroids Remdesivir Consultants following: ID Anticipated special isolation end date: 10/15/2023 Encourage prone position as tolerated Type 2 diabetes uncontrolled Last A1c 5.7 I will hold insulin 70/30 24 twice a day Start Lantus 20 units at bedtime, Humalog 8 units every meal plus sliding scale Hold Trulicity in the hospital Start Januvia 100 mg once daily instead Hold metformin Hypertension Continue losartan Hold Lasix- continue at discharge Hypothyroidism Continue levothyroxine GERD Continue Protonix Hyperlipidemia Continue Zetia Neuropathy Continue gabapentin Nicotine use disorder Advised smoking cessation Start nicotine patch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 23.08.2023
- Impfdatum
- 07.10.2022
- Beginn
- 09.03.2023
- Tage bis Beginn
- 153,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
Angina unstable
Arteriosclerosis
Arteriosclerosis coronary artery
Symptomtext
I21.3 ACUTE ST ELEVATION MI, UNSPECIFIED 3/16/2023 ASHD NATIVE COR ART W/UNSTABLE ANGINA PECTORIS I21.3 ACUTE ST ELEVATION MI, UNSPECIFIED 3/16/2023 NON-ST ELEVATION MYOCARDIAL INFARCTION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 15.08.2023
- Impfdatum
- 17.10.2022
- Beginn
- 02.03.2023
- Tage bis Beginn
- 136,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Ischaemic stroke
Lacunar stroke
Lung adenocarcinoma
Symptomtext
I63.81 ACUTE LACUNAR STROKE, UNSPECIFIED TYPE AND ARTERY 3/23/2023 ADENOCARCINOMA LUNG, UNSPECIFIED SITE I63.9 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 3/24/2023 ADENOCARCINOMA LUNG, UNSPECIFIED SITE J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 3/24/2023 ADENOCARCINOMA LUNG, UNSPECIFIED SITE I63.81 ACUTE LACUNAR STROKE, UNSPECIFIED TYPE AND ARTERY 3/23/2023 ADENOCARCINOMA LUNG, UNSPECIFIED SITE I63.9 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 3/24/2023 ADENOCARCINOMA LUNG, UNSPECIFIED SITE J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 3/24/2023 ADENOCARCINOMA LUNG, UNSPECIFIED SITE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 19.07.2023
- Impfdatum
- 01.12.2022
- Beginn
- 02.05.2023
- Tage bis Beginn
- 152,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
Blood creatinine increased
COVID-19
Chest X-ray normal
Cough
Hyperglycaemia
Hypertension
Hypoxia
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Patient is a 60 y.o. female patient of, MD with history of diabetes mellitus type 2 on insulin, hypertension, hyperlipidemia who presented to Hospital with hyperglycemia, hypoxia and fever. Patient was transferred from ED Acute respiratory failure with hypoxia COVID-19 infection Date of onset of symptoms: 5/1/23 Symptoms present on admission: fever, sore throat, dry cough Date of covid positive test: 5/2/23 Vaccination status: vaccinated Imaging: CXR no acute focal infiltrate Oxygen requirements on admission: 2L NC Current oxygen requirements: Currently weaned to room air Infectious disease following Continue Decadron, remdesivir Stable for discharge home Hyperglycemia Diabetes mellitus type 2 on insulin A1c 10.4 up from 10, 5 months ago Labs on admission with normal bicarb and anion gap with glucose 332 States she is taking Lantus 17 units nightly, Farxiga 10 mg daily and metformin 2000 mg nightly. Lantus 25 units nightly plus SSI. Adjust as needed AKI - resolved At OLH creatinine was 1.86 ->1.13 >1.17 baseline 1.1?1.3 Avoid nephrotoxic agents Hypertension Takes amlodipine 5 mg nightly at home and hydrochlorothiazide 25 mg daily Continue amlodipine. Resume hydrochlorothiazide
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 13.07.2023
- Impfdatum
- 15.12.2022
- Beginn
- 28.03.2023
- Tage bis Beginn
- 103,0
- Dosis
- 4
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Anaemia
Coagulopathy
Symptomtext
COAGULOPATHY, UNSPECIFIED TYPE 3/28/2023 ANEMIA ACUTE RESPIRATORY FAILURE 3/28/2023 ANEMIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 11.07.2023
- Impfdatum
- 30.10.2022
- Beginn
- 24.02.2023
- Tage bis Beginn
- 117,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Neuropathy peripheral
Sleep apnoea syndrome
Symptomtext
MIXED SLEEP APNEA NEUROPATHY ACUTE HYPOXEMIC RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 10.07.2023
- Impfdatum
- 05.11.2022
- Beginn
- 20.02.2023
- Tage bis Beginn
- 107,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pulmonary embolism
Symptomtext
ACUTE PULMONARY EMBOLISM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 10.07.2023
- Impfdatum
- 14.10.2022
- Beginn
- 31.03.2023
- Tage bis Beginn
- 168,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Anaemia
Atrial fibrillation
Blood creatinine
Blood loss anaemia
Blood pressure decreased
COVID-19
Cardiac failure
Cardiac failure acute
Chest X-ray normal
Condition aggravated
Coronary arterial stent insertion
Coronary artery bypass
Coronary artery disease
Device failure
Diabetic diet
Echocardiogram normal
Ejection fraction
Symptomtext
Patient is a 85 y.o. female patient of, MD with history of CAD, CKD 3, DM 2, GERD, hyperlipidemia, CHF, hypertension, PVD, OSA presented on 3/31/2023 with hip fracture. Found to have COVID with hypoxia. Treated with Decadron and remdesivir, clinically improved, saturating well on room air for the last 24 hours, feels comfortable going home instead of rehab Right hip FNS implant failure S/p right hip removal of hardware and hemiarthroplasty Continue postop care as per Ortho Continue PT OT Acute respiratory failure with hypoxia Covid-19 Virus Infection Date of onset of symptoms: Asymptomatic Symptoms present on admission: Asymptomatic Date of covid positive test: 4/2/2023 Vaccination status: vaccinated Imaging: Chest x-ray 4/4/2023?no abnormality Oxygen requirements on admission: Room air Current oxygen requirements: Room air Medical therapy: Decadron and remdesivir 4/4/2023-4/5/23 Consultants following: None Anticipated special isolation end date: 4/11/2023 Acute on chronic HFpEF CAD s/p CABG and stent to RCA PVD Responding well to IV Lasix Switch back to home dose of Lasix 40 mg p.o. twice daily Echo 8/2022 LVEF 60% Continue asa, statin, lasix, imdur, metoprolol, nifedipine, Entresto Orthostatic hypotension?resolved Blood pressure dropped on 4/2, 4/3 after working with physical therapy Responded well to IV fluid bolus Clinically improving, feels comfortable going home Continue nifedipine and metoprolol with holding parameters DM2 A1c 7.4 SSI Diabetic diet CKD3b Scr 1.62 Baseline range from 1.4-1.6 Monitor renal function Encourage p.o. hydration, holding Lasix, Entresto Acute on chronic anemia Anemia of chronic kidney disease worsened secondary to blood loss associated from surgery Hemoglobin 8.9<9.0<10.1 Continue to monitor Chronic afib Rate controlled Asa, plavix OSA CPAP ordered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 04.07.2023
- Impfdatum
- 28.10.2022
- Beginn
- 04.04.2023
- Tage bis Beginn
- 158,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
Asthenia
Atelectasis
Blood creatinine increased
Bronchitis
COVID-19
Computerised tomogram thorax abnormal
Condition aggravated
Cough
Diarrhoea
Dyspnoea
Gastrointestinal disorder
Hyperglycaemia
Hypoxia
Ileus
Intestinal obstruction
Lung opacity
Symptomtext
The patient is a 75 y.o. female patient of a CNP with history of HTN, HLD, multiple hernia repairs, asthma, recent admission for ileus and bronchitis(dc 3/28) who presented to the Medical Center with cough, wheeze, dyspnea, generalized weakness, N/V/D. Acute hypoxemic respiratory failure Covid-19 Virus Infection Community acquired pneumonia Dyspnea, hypoxia requiring 4LNC Multifactorial due to COVID and pneumonia CT chest in ED with dependent opacities atelectasis favored vs PNA; also nodule Date of onset of COVID symptoms: 3/11 Date of covid positive test: 4/4 Vaccination status: vaccinated Imaging: As above Oxygen requirements on admission: 4L Current oxygen requirements: RA Urine antigen neg, sputum cx mixed flora Medical therapy: steroids, rocephin, and zithromax; started remdesivir as GI symptoms consistent with new COVID Consultants following: none Anticipated special isolation end date: 4/14 Home oxygen evaluation completed and no home O2 needs identified; discharged on RA Ileus Dx last admission; improved since Returns with GI symptoms again; although could all be COVID-related KUB on admission ileus vs mild bowel obstruction Passing BM's; last was 1d PTA Tolerated regular diet Continue bowel regimen AKI Cr up to 2.02 on 4/5 from baseline ~1 Likely prerenal due to GI losses Continue hydration for now SCr improved to 0.80 on 4/8 Steroid-induced Hyperglycemia BG ~100-200 since admission Likely due to steroids Monitor for now Lung nodule RUL 1.7 cm nodule seen on CT, with borderline enlarged R hilar mediastinal LN Rec recheck CT in 3 months, PET-CT or tissue sampling Generalized weakness Myalgia Due to current illness Uses a walker at baseline Re-assess after treatment Mobilize as able Muscle aches likely related to COVID Norco prn ordered HTN Holding home hydrochlorothiazide and losartan for AKI Continue home Norvasc and clonidine Hx of Paradoxical VCD Hx of Polypoid corditis ENT consulted previous admission discovered 3/14 Laryngeal control therapy breathing exercises and outpt ENT f/u
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 26.06.2023
- Impfdatum
- 22.09.2022
- Beginn
- 30.03.2023
- Tage bis Beginn
- 189,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
Chronic respiratory failure
Obstructive sleep apnoea syndrome
Respiratory failure
Symptomtext
I21.4 ACUTE NON ST ELEVATION MI 4/4/2023 ADULT OBSTRUCTIVE SLEEP APNEA, MODERATE J96.11 CHRONIC HYPOXEMIC RESPIRATORY FAILURE 1/4/2023 ADULT OBSTRUCTIVE SLEEP APNEA, MODERATE I21.4 ACUTE NON ST ELEVATION MI 4/4/2023 ACUTE NON ST ELEVATION MI J96.11 CHRONIC HYPOXEMIC RESPIRATORY FAILURE 1/4/2023 ACUTE NON ST ELEVATION MI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 02.06.2023
- Impfdatum
- 29.09.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 34,0
- Dosis
- 5
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Atrioventricular block second degree
Cardiac failure congestive
Chronic left ventricular failure
Chronic respiratory failure
Condition aggravated
Dyspnoea
Respiratory failure
Symptomtext
ACUTE HYPOXEMIC RESPIRATORY FAILURE 12/29/2022 DYSPNEA CHRONIC HYPOXEMIC RESPIRATORY FAILURE 10/31/2022 DYSPNEA RESPIRATORY FAILURE, UNSPECIFIED ACUITY 11/21/2022 DYSPNEA ACUTE HYPOXEMIC RESPIRATORY FAILURE 12/29/2022 CHF EXACERBATION, UNSPECIFIED CHRONIC HYPOXEMIC RESPIRATORY FAILURE 10/31/2022 CHF EXACERBATION, UNSPECIFIED RESPIRATORY FAILURE, UNSPECIFIED ACUITY 11/21/2022 CHF EXACERBATION, UNSPECIFIED ACUTE HYPOXEMIC RESPIRATORY FAILURE 12/29/2022 AV BLOCK, MOBITZ TYPE 2 CHRONIC HYPOXEMIC RESPIRATORY FAILURE 10/31/2022 AV BLOCK, MOBITZ TYPE 2 RESPIRATORY FAILURE, UNSPECIFIED ACUITY 11/21/2022 AV BLOCK, MOBITZ TYPE 2 ACUTE HYPOXEMIC RESPIRATORY FAILURE 12/29/2022 SYSTOLIC HEART FAILURE, CHRONIC CHRONIC HYPOXEMIC RESPIRATORY FAILURE 10/31/2022 SYSTOLIC HEART FAILURE, CHRONIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 11/21/2022 SYSTOLIC HEART FAILURE, CHRONIC ACUTE HYPOXEMIC RESPIRATORY FAILURE 12/29/2022 SYSTOLIC HEART FAILURE, CHRONIC CHRONIC HYPOXEMIC RESPIRATORY FAILURE 10/31/2022 SYSTOLIC HEART FAILURE, CHRONIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY 11/21/2022 SYSTOLIC HEART FAILURE, CHRONIC
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 02.06.2023
- Impfdatum
- 22.11.2022
- Beginn
- 26.02.2023
- Tage bis Beginn
- 96,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
Chills
Chronic obstructive pulmonary disease
Condition aggravated
Cough
Dyspnoea
Exposure to SARS-CoV-2
SARS-CoV-2 test positive
Sputum discoloured
Symptomtext
Patient with a history of COPD. She presented to the ED on 2/26/23 with a week's worth of symptoms including shortness of breath, cough, chills, and green phlegm. She notes she was exposed to a friend who tested positive for COVID. A COVID-19 PCR test performed in the ED resulted positive. She was placed on 2L supplemental O2 with O2 sats at 95%. Ultimately she was admitted 2/26/23-2/28/23 with discharge diagnoses including acute hypoxic respiratory failure d/t AECOPD, possible bacterial bronchitis, and COVID-19 infection. She was started on Dexamethasone 6mg daily (started 2/26) and required supplemental O2. She was eventually weaned to room air. Of note, the patient has received the primary COVID vaccine series and three boosters.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 02.06.2023
- Impfdatum
- 07.10.2022
- Beginn
- 08.01.2023
- Tage bis Beginn
- 93,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Dementia Alzheimer's type
Symptomtext
J96.01 ACUTE HYPOXEMIC RESPIRATORY FAILURE 1/8/2023 ALZHEIMERS DISEASE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 11.05.2023
- Impfdatum
- 11.11.2022
- Beginn
- 08.05.2023
- Tage bis Beginn
- 178,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute respiratory failure
Anticoagulant therapy
Anxiety
Arthropathy
Atrial fibrillation
C-reactive protein increased
COVID-19
Cardiac failure congestive
Chronic left ventricular failure
Condition aggravated
Coronary artery disease
Dyslipidaemia
Dyspnoea
Fatigue
Hypertension
Left atrial appendage closure implant
Metabolic function test normal
Neuropathy peripheral
Symptomtext
Discharge Provider: DO Primary Care Provider at Discharge: DO Admission Date: 5/8/2023 Discharge Date: 05/10/2023 Discharge Disposition: Home DISCHARGE DIAGNOSIS: 1. Severe COVID-19 infection with acute hypoxic respiratory failure 2. Permanent AFib status post ablation 2019 and Watchman 2023 3. Chronic diastolic CHF 4. Hypertension 5. Dyslipidemia 6. Coronary artery disease in right coronary artery 7. History of stroke 8. Venous insufficiency 9. History of cancer 10. Neuropathy 11. Anxiety 12. Obesity PRESENTING PROBLEM: Severe COVID-19 infection with acute hypoxic respiratory failure HOSPITAL COURSE: Patient was admitted to the hospital on 05/08/2023 with reports of fatigue for the past 6 weeks knee and shortness of breath since 05/05/2023. She has a history of diastolic CHF, permanent Afib, and history of stroke. She is currently anticoagulated with warfarin, aspirin, and Plavix. She was tested for COVID and was found to be positive on 05/08 she was given dose of Solu-Medrol and was begun on remdesivir. Her oxygen saturation dropped to 84% with ambulation, but she was able to improved to greater than 90% on room air with rest. PT and OT screen the patient and reported that she was independent with all mobility and did not need skilled PT or OT at this time. She was continued with oral Decadron as well as Mucinex and Tessalon. Her CMP was monitored throughout her hospital stay and were grossly within normal limits. Her CRP improved from 11.4 to 4.6. She reported improvement with her symptoms after 3 days of remdesivir. She had no further concerns, and was discharged home in improved in stable condition
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Anemia GERD (gastroesophageal reflux disease) Essential hypertension CAD (coronary artery disease) Hyperlipidemia Dilated aortic root Permanent atrial fibrillation Injury of phrenic nerve Asthma with COPD, severe Hemidiaphragm paralysis Mixed spasmodic dysphonia Pulmonary HTN Syncope, near Carotid artery disease Valvular heart disease Squamous cell carcinoma of anus Cardiomyopathy LVH (left ventricular hypertrophy) Diastolic dysfunction Atrial enlargement, bilateral Senile osteoporosis CHF (congestive heart failure) Chronic anticoagulation H/O: CVA (cerebrovascular accident) Contrast media allergy Microvascular embolism of arteriole
- Andere Medikamente
- acetaminophen (TYLENOL) 500 mg tablet aspirin 81 MG enteric coated tablet atorvastatin (LIPITOR) 80 MG tablet Azelaic Acid 15 % GEL benzonatate (TESSALON) 100 MG capsule buPROPion (WELLBUTRIN XL) 150 mg 24 hr tablet Calcium Carbonate-Vitami
- Allergien
- Diagnostic X-ray MaterialsShortness of Breath Dye-contrastShortness of Breath CodeineNausea Only, Other Pet Dander
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 03.05.2023
- Impfdatum
- 15.11.2022
- Beginn
- 19.12.2022
- Tage bis Beginn
- 34,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Anticoagulant therapy
Anxiety
Back pain
Blood test normal
COVID-19
Chest pain
Computerised tomogram thorax abnormal
Deep vein thrombosis
Dizziness
Echocardiogram normal
Electrocardiogram normal
Fatigue
Foot operation
Pulmonary embolism
SARS-CoV-2 test positive
Scan with contrast abnormal
Ultrasound Doppler abnormal
Symptomtext
12/19/22 I started having pain in my chest and back. I was tired. The next day, I continued with these symptoms. That night I started worrying it could be a pulmonary embolism. The next day, I was lightheaded when I stood up so I went to the Emergency Room on 12/21/22. It was confirmed I had a DVT and a pulmonary embolism. (I had foot surgery on 12/9/22, unrelated.) I was tested for COVID in the Emergency Room on 12/21/22 and it was positive. I was told it was provoked due to the combination of the foot surgery and I was at increased risk because of having COVID. I was admitted to the hospital overnight. I started on Eliquis and took it for 3 months. I have had no symptoms or blood clots since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 2,0
- Labordaten
- 21DEC22-COVID Test-Positive; 21DEC22-ECG- Normal; 21DEC22-Echocardiogram-Normal; 21DEC22-Leg UltraSound-Blood Clot in left leg; 21 DEC23-Bloodwork-Normal; 21DEC23-CT with Contrast of Chest-Pulmonary Embolism;
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, Irritable Bowel Syndrome, Gastro esophageal disease
- Andere Medikamente
- Flovent, Claritin, Singular, Colestipol, Omeprazole, Miralax
- Allergien
- Penicillin, Sulfa Drugs, Cantaloupe, Honey Dew, Walnuts, Hazelnuts
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 03.03.2023
- Impfdatum
- 05.12.2022
- Beginn
- 23.02.2023
- Tage bis Beginn
- 80,0
- Dosis
- 5
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Respiratory arrest
Unresponsive to stimuli
Symptomtext
02/23/2023: At 1:55am resident was found unresponsive, no respirations noted, unable to revive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hx CVA, diabetes type 2, Dysphagia, Aphasia, Unspecified atherosclerosis of native arteries of extremities, bilateral legs, essential hypertension, gout,
- Andere Medikamente
- Colace, Glucophage, Lyrica, Lipitor, Levemir, Hyzaar, Zoloft, Colcrys, Cephulac, Linzess,
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 03.03.2023
- Impfdatum
- 05.12.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Dyspnoea
Myocardial infarction
Oxygen saturation decreased
Pneumonia
Symptomtext
12/06/23 05:00 a.m. Resident voiced complaints of SOB at around 0005. Vitals collected O2 SAT recording low 80% on 2LNC. BP 113/75 HR 134 R-28 Temp 98. Resident stated to writer, "I can't breathe". Sent to emergency room and admitted with dx of myocardial infarction and pna, returned to facility on 12/7/23, went under hospice care on 12/9/23 and expired on 12/23/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- chronic respiratory failure, COPD, hypothyroidism, chronic CHF, essential hypertension, atherosclerotic heart disease of native coronary artery, CKS, pulmonary hypertension, anemia, atrial fibrillation, anxiety, non-rheumatic mitral and tricuspid valve insufficiency, emphysema, osteoarthritis, GERD,
- Andere Medikamente
- Abilify, Zoloft, Wellbutrin, Protonix, Colace, Neurontin, Synthroid, Culturelle, Bystolic, Multivitamin, Lasix, Folic Acid, Iron, Vitamin D3, Vitamin C
- Allergien
- epinephrine, penicillin's
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 25.02.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.01.2023
- Tage bis Beginn
- 92,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute left ventricular failure
Acute respiratory failure
Angiogram pulmonary abnormal
Blood creatinine increased
COVID-19
Computerised tomogram thorax abnormal
Condition aggravated
Diuretic therapy
Dyspnoea
Echocardiogram abnormal
COVID-19 pneumonia
Cardiac failure congestive
Cardiac ventricular disorder
Cardiomegaly
Chronic obstructive pulmonary disease
Effusion
Ejection fraction normal
Glycosylated haemoglobin normal
Symptomtext
Patient is a 66 y.o. female patient of MD with history of COPD, CKD, type 2 diabetes, hypertension presented to Doctors Hospital with SOB Discharge Diagnoses: Acute on chronic respiratory failure with hypoxia Multifactorial including COVID, severe Pulm HTN, COPD exacerbation Required BiPAP-- > non-heated Hiflo, Pulm following Wears 4L of O2 at baseline Attempted to wean down over the weekend but requirement went up but contines to wean down Continue diuresis Pulmonary on board Repeat Home O2 eval done; qualifies for 6L as new requirement Covid-19 Pneumonia Date of onset of symptoms: 1-2 Days prior to admission Symptoms present on admission: SOB, Hypoxia Date of covid positive test: 01/12/2023 Vaccination status: vaccinated Imaging: CTPA study no PE small right pleural effusion with small right lung base consolidation. Oxygen requirements on admission: BIPAP Current oxygen requirements: Heated hiflo Medical therapy: steroids at present Consultants following: ID, pulmonology Anticipated special isolation end date: 01/22/2023 Completed abx, remdesivir and dexa ID on board Acute COPD exacerbation Patient has history of COPD, baseline 4L O2 Uses Breo Ellipta 200-25 MCG at home Start Symbicort and Spiriva, needed albuterol inhalation Completed steroid Acute Diastolic Congestive Heart failure Severe tricuspid valve regurgitation Severe pulmonary hypertension No previous history of CHF Presented with lower extremity edema and effusion on CT chest Echo showed EF 66%, significant pulmonary hypertension with estimated right ventricular systolic pressure 47 mmHg right chamber mildly enlarged slight systolic function reduced. Not on diuretics at home. CT with signs of right-sided heart failure Updated ECHO showed EF 55-60% with septal flattening consistent with RV volume and pressure overload with severely dilated and reduced function of RV with severe functional tricuspid valve regurgitation with hepatic vein systolic flow reversal. Severe hypertension noted with RVSP 90 Cardiology consulted?change could be related to COVID-19 infection. Recommend gentle diuresis for what appears to be right-sided failure. Needs further cardiac work up, RHC when stable on OP basis Continue lasix for diuresis Pulm on board History of CAD S/p PCI to OM and RCA Continue Lipitor Not taking aspirin, resume CKD stage III Baseline creatinine 1.3-1.4, this am 1.46 Monitor renal function Essential Hypertension On lisinopril 10 mg at home Currently being held while on IV diuretics due to underlying CKD As needed hydralazine. BP stable. DM 2 w hyperglycemia Last hemoglobin A1c 5.7 on glipizide and Actos at home both being held Will have to discontinue Actos due to CHF prior to discharge Glu elevated to do decadron, add lantus cont SSI\ Abnormal CT CT showed irregular parenchymal density seen in the right apex measuring up to 15 mm which appears more pronounced compared with prior exam. Which may represent scarring. However nodular scarring and malignant etiology cannot be excluded. Correlation and continued follow-up imaging with possible PET/CT imaging may be considered. Pulmonology consulted as above Can have outpatient follow-up and biopsy as clinically warranted Tobacco abuse. Cessation has been advised Continue NRT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 27.11.2022
- Beginn
- 29.11.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cerebrovascular accident
Symptomtext
Patient's wife states that she woke up next to her husband 2 days post vaccination and realized he was having a stroke. He was immediately hospitalized.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Cephalexin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 15.02.2023
- Impfdatum
- 18.11.2022
- Beginn
- 17.01.2023
- Tage bis Beginn
- 60,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal discomfort
Acute kidney injury
Acute myocardial infarction
Antiplatelet therapy
Bile duct stone
Biliary dilatation
Bladder hypertrophy
Bladder irrigation
Blood creatinine increased
Blood culture negative
Blood loss anaemia
Computerised tomogram abdomen abnormal
Diarrhoea
Diverticulitis
Gastrointestinal haemorrhage
Haematochezia
Hepatic enzyme
Leukocytosis
Symptomtext
She is a 94 y.o. female patient of DO with history of GI bleed and diverticulosis who presented to the Hospital with complaint of diarrhea, LLQ discomfort and bright red blood in stool. She had a recent NSTEMI a couple of weeks ago at which time DAPT was restarted. She was found to have acute splenic flexure diverticulitis. Acute diverticulitis History of diverticulosis. CT with acute splenic flexure diverticulitis. Blood Cx-no growth Continue Zosyn (day #3)- switch to oral antibiotics tomorrow- Cipro 500 mg oral daily and Flagyl 500 mg oral every 8 hours-for 7 days Pain management prn Monitor WBC GI bleed Hematochezia Acute Anemia -blood loss Hgb 11.2> 10.1>10.3>9.0 Unremarkable EGD in 8/20/22, flex sig at that time showed sigmoid diverticulosis. Hold Plavix, continue aspirin. HOLD Plavix secondary to GI bleed- patient instructed to follow up with Cardiology to discuss re-starting this medication- patient wishes not to restart at this time due to bleeding Continue Protonix General surgery following- no indication for acute endoscopic intervention Gastroenterology signed off- follow up with PCP Tolerating full liquid diet- advance as tolerated Choledocholithiasis Noncontrast CT with choledocholithiasis within the distal common bile duct with common bile duct distention. Unremarkable hepatobiliary enzymes. GI evaluating, may not pursue ERCP as asymptomatic, and with advanced age. General surgery following-signed off no surgical intervention Urinary bladder thickening Reviewed CT finding of urinary bladder thickening with surrounding fat stranding and intraluminal air. Patient reported bladder irrigation the day prior to presentation. Monitor urine output and any urinary symptoms. Leukocytosis WBC- 12.22>11.0>8.38 Afebrile Monitor CBC Chronic combined systolic and diastolic CHF CAD Last 2D echo of 8/2022 with LVEF of 39%, grade 2 diastolic dysfunction. Recent NSTEMI 1/17/23 Continue medical management.-hold Plavix Daily weights Strict I & 0's Essential hypertension Hyperlipidemia BP is controlled. Continue metoprolol, Zestril. Atorvastatin AKI Creatinine of 1.49>1.31>1.45>1.51 Recent bladder irrigation. Avoid nephrotoxins. Monitor BMP Strict I & O's
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 12.02.2023
- Impfdatum
- 17.10.2022
- Beginn
- 29.01.2023
- Tage bis Beginn
- 104,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Angiogram pulmonary abnormal
Anticoagulant therapy
Atrial fibrillation
Blood bicarbonate normal
Blood gases abnormal
Blood pH normal
CHA2DS2-VASc-score
COVID-19
Cardiac failure
Confusional state
Deep vein thrombosis
Echocardiogram abnormal
Ejection fraction decreased
Electrocardiogram abnormal
Hypercoagulation
Leukocytosis
Lung consolidation
Symptomtext
Acute Hypoxemic, Hypercapnic Respiratory Failure, resolved - Secondary to bilateral PEs and COVID-19 infection below, on room air at baseline - 1/28 VBG: pH 7.41, pCO2 37.7, pO2 50, HCO3 24.0 - Weaned to room air with treatment as below Intermediate-Low Risk Pulmonary Embolism - Bilateral LE DVTs below with elevated troponin's and evidence of right heart strain on imaging, PESI: 117, Class IV, High Risk - 1/28 CT PA large PE within bilateral main pulmonary arteries of all lung lobes, evidence of right heart strain, pulmonary artery enlarged, moderate leukocytosis - 1/29 TTE normal RV dimensions and function, possible pulmonary hypertension - Peripheral Vascular followed, transitioned to Xarelto, follow up with PV in 1 month as outpatient Bilateral Lower Extremity DVTs - In the setting of hypercoagulable state secondary to COVID-19 infection - 1/28 LE dopplers: DVT in left gastrocnemius, DVTs reaching as superiorly as popliteal vein on the right - Continue anticoagulation per above COVID-19 Infection Community Acquired Pneumonia - Patient denies any symptoms or sick contacts, received 3 vaccines (uncertain which ones) - 1/28 COVID-19 PCR positive, CT PA focal consolidation bilateral lower lobes, regional area groundglass opacity in right lower lobe, moderate leukocytosis - S/p ceftriaxone 1/29, azithromycin (1/29-1/30) and decadron 6 mg (1/28-1/30) - Will complete 4 days of po Augmentin for treatment of CAP Paroxysmal Atrial Fibrillation with RVR - Likely secondary to heart strain due to PE, per patient no history of atrial fibrillation - 1/28 EKG may have been sinus rhythm with frequent PACs causing confusion for atrial fibrillation - CHADS-VASc = 4 - Will be discharged on Xarelto as above with outpatient follow-up with peripheral vascular Elevated Troponin - Most likely Type II Demand Ischemia in setting of PE above - Trop 51 -> 45, negative delta Leukocytosis, resolving - Reactive in setting of above - WBC 20.77 on admission decreased to 17K on discharge - Repeat CBC in 1 week HF recovered EF - 4/22/21 TTE LVEF 20-25% - 1/29/23 TTE LVEF 61% - Home medication: losartan 25 mg daily - Consider escalating therapy with addition of beta blocker and SGLT2 inhibitor
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 27.11.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 5,0
- Dosis
- 5
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Angiogram cerebral
Arteriogram carotid
Blood test
Cerebrovascular accident
Chest X-ray
Computerised tomogram abdomen
Computerised tomogram head abnormal
Confusional state
Echocardiogram
Headache
Ischaemic stroke
Magnetic resonance imaging head abnormal
Scan with contrast
Urine analysis normal
Vomiting
Symptomtext
5 days following the vaccination, Patient suffered an ischemic stroke. It was initially thought perhaps a UTI, due to the signs (confusion, vomiting, headache). But the urine sample came back negative so she was taken to the ER by ambulance, where CT-scans and 2 MRI's were done, confirming the stroke (multiple strokes in the brain, but very small) and no bleeding. After 5 days in the hospital, she spent 3 weeks in a rehab and is now back at her Assisted Living facility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 27,0
- Labordaten
- 2 CT Scans of head w/o contrast - 12/4/22 and 12/5/22 CT Abdomen and pelvis with IV Contrast - 12/4/22 XRay Chest - 12/4/22 MRI Brain w/o contrast - 12/5/22 Blood Work - 12/4/22, 12/5/22, 12/6/22, 12/9/22, 12/10/22, 12/12/22, 12/19/22, 12/26/22 Transthoracic Echo Complete - 12/6/22 MRI Angio Head w/o contrast - 12/6/22 MRI Angio Neck w/o contrast - 12/6/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure (controlled), Chronic Lung Infection
- Andere Medikamente
- Amlodipine, Aspirin, Atorvastatin, Citalopram, Lisinopril, Metoprolol, Azithromycin, Ethambutol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 02.11.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 29,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Anticoagulant therapy
Asthenia
Blood test
Cerebrovascular accident
Computerised tomogram
Hemiparesis
Magnetic resonance imaging
Neurological symptom
Transient ischaemic attack
Symptomtext
TIA stroke requiring hospitalization overnight. Symptoms were vertigo like, left sided weakness. Treatment included statin, plavix, aspirin. Not sure its related to covid vaccine but wanted it reported just in case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 2,0
- Labordaten
- Bloodwork, ct, mri
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- none
- Andere Medikamente
- Multivitamin
- Allergien
- motrin
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 18.01.2023
- Impfdatum
- 29.11.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cerebrovascular accident
Intensive care
Laboratory test
Scan
Symptomtext
Stroke less than 24 hours of injection; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 29Nov2022 as dose 4 (booster), single (Batch/Lot number: unknown) at the age of 64 years, in right 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, SINGLE), for COVID-19 immunization; Covid-19 vaccine (DOSE 2, SINGLE), for COVID-19 immunization; Covid-19 vaccine (DOSE 3 (BOOSTER), SINGLE), for COVID-19 immunization. The following information was reported: CEREBROVASCULAR ACCIDENT (hospitalization, medically significant, life threatening) with onset 30Nov2022 at 02:00, outcome "not recovered", described as "Stroke less than 24 hours of injection". The patient underwent the following laboratory tests and procedures: Scan: Unknown results. Therapeutic measures were taken as a result of cerebrovascular accident. Clinical course: No other vaccine in four weeks. AE treatment: ICU, numerous scans. No covid prior vaccination and not tested post vaccination. The information on the batch/lot number for BNT162b2, BNT162b2 omi ba.4-5 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- Test Name: numerous scans; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 16.01.2023
- Impfdatum
- 23.10.2022
- Beginn
- 09.11.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cerebrovascular accident
Spinal decompression
Symptomtext
Patient experienced stroke 17 days post Covid vaccine. She had also had lumbar decompression/fusion surgery earlier on the day of the stroke. She had a history of lower extremity DVT managed on Eliquis prior to admission.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Lumbar decompression/fusion
- Vorgeschichte
- Asthma, migraines, previous DVT on Eliquis, hypertension, hyperlipidemia, CREST syndrome
- Andere Medikamente
- Prednisone, Tobradex, Flovent, apixaban, acetaminophen, ferrou
- Allergien
- Adhesive, aurothiomalic acid disodium, benzoic acid, cobalt, d
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 12.11.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 24,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Angiogram pulmonary abnormal
Dyspnoea
Pulmonary embolism
Symptomtext
bilateral pulmonary embolism; patient reports onset symptoms 12/06/2022; did not seek evaluation until 01/06/2023 when presented with shortness of breath that had onset 12/06/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 2,0
- Labordaten
- CT angio chest 01/06/2023 = "multiple bilateral pulmonary emboli"
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- mild LDL cholesterol elevation
- Andere Medikamente
- none
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 18.12.2022
- Tage bis Beginn
- 12,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Patient expired within 90 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 28.11.2022
- Impfdatum
- 14.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 8,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
White blood cell count increased
Symptomtext
Resident Expired
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- WBC 21.50 on 11/21/22 started on Ceftriaxone
- Aktuelle Erkrankungen
- Aneurysm of the heart, Diabetes mellitus, Fracture of the femur, dementia with psychotic disorder
- Vorgeschichte
- Diabetes Mellitus, Heart Aneurysm
- Andere Medikamente
- Metoprolol, Lovenox injection, Lantus Insulin, Vitron C, Ferrous Sulfate, Folic acid, Atorvastatin, Quetiapine, sertraline, trazodone, Metformin
- Allergien
- Demerol
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 13.11.2022
- Impfdatum
- 29.09.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 22,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Anticoagulant therapy
Asthma
Blood creatinine normal
Bronchiectasis
COVID-19
COVID-19 pneumonia
Chest X-ray normal
Chronic kidney disease
Essential hypertension
Gastrooesophageal reflux disease
Glycosylated haemoglobin increased
Hyperlipidaemia
SARS-CoV-2 test positive
Type 2 diabetes mellitus
Symptomtext
Patient is a 85 y.o. female admitted to the hospital on 10/21/2022 for COVID-19. Discharge Diagnosis and Associated Hospital Course Acute respiratory failure with hypoxia, resolved ? Likely due to COVID-19 pneumonia ? Oxygen saturation on 86% on room air at presentation, currently 96% on RA COVID-19 infection ? Symptoms started approximately a week prior to arrival and progressively worsened over the last 3 days prior to admission ?Positive COVID-19 screening test on 10/21/2022 ? Vaccinated and boosted. Last vaccine 9/29/2022 ? Chest x-ray does not show any definitive infiltrate ? Currently saturating 96% on RA ? Steroids: Decadron 10 mg daily, home on prednisone burst given underlying bronchiectasis ? Antiviral: Remdesivir received one dose, no further doses needed as she is much improved and no longer requiring oxygen ? DVT prophylaxis: Lovenox Essential hypertension ? Chronic and stable ? Continue home metoprolol, triamterene?hydrochlorothiazide, amlodipine Mild persistent intermittent asthma ? Fairly well controlled ? Compliant with home Advair and rescue inhaler ? Continue home inhalers Diabetes mellitus type 2 with CKD stage III ? Chronic and stable ? Hemoglobin A1c 6.4 ? Compliant with home metformin ? Hold metformin ? Continue insulin sliding scale and diabetic diet ? Monitor blood glucose closely in the setting of steroids Chronic kidney disease stage IIIa ? Creatinine remains stable at around 1.1 ? Avoid nephrotoxic agents and renally dose medications as appropriate ? Recommend continued outpatient follow-up with PCP Hyperlipidemia ? Continue home statin History of bronchiectasis ? Uncomplicated - discharged with steroid taper as above GERD without esophagitis ? Continue home PPI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 09.11.2022
- Impfdatum
- 26.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Computerised tomogram thorax abnormal
Deep vein thrombosis
Muscle spasms
Pain in extremity
Peripheral swelling
Pulmonary embolism
Ultrasound Doppler abnormal
Symptomtext
Patient experienced DVT in right leg and pulmonary embolism. Symptoms of DVT included cramping, swelling, and pain right leg, which started 10/28/22. Patient was seen by healthcare provider on 11/3/22 and diagnosed at that time with DVT/PE then started on Eliquis and Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- Doppler 11/4/22 in right and left leg CT scan 11/3/22 (lungs)
- Aktuelle Erkrankungen
- Treatment for endometrial cancer (now cancer free) Common cold (not COVID-19 tested)
- Vorgeschichte
- Endometrial cancer
- Andere Medikamente
- Propranolol 20mg - 1 tablet by mouth three times per day Trazodone 50mg - 1 tablet by mouth every night Methylphenidate 10mg - 15mg by mouth two times per day Triamcinolone 0.1% paste- apply to sores in mouth three times per day as needed D
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- U
- Eingang
- 18.10.2023
- Impfdatum
- 01.11.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bell's palsy
Symptomtext
Bells Palsey; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A patient (no qualifiers provided) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), in Nov2022 as dose number unknown (booster), single (Batch/Lot number: unknown) 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 immunisation. The following information was reported: BELL'S PALSY (medically significant) with onset 2022, 3 days after the suspect product(s) administration, outcome "recovered" (2023), described as "Bells Palsey". Clinical course: Patient received COVID booster last year in Nov. Three days later patient got Bells Palsy. Patient called # where patient got it to let them know. They said they had a couple of other people report that too. We searched Pfizer about it, it said Yes, it could happen but there was not enough statistics to do a report. Patient was worried to get another vaccine, as patient was sick for 6 months. Patient's 84-year-old mother caught the Bells Palsy from patient two months after patient got it. It was a virus. The information on the batch/lot number for bnt162b2, bnt162b2 omi ba.4-5 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 16.08.2023
- Impfdatum
- 20.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pericarditis
Pyrexia
Symptomtext
Postvaccination fever on 2022-10-21, Acute nonspecific idiopathic pericarditis on 2022-11-03.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- LOSARTAN POTASSIUM 50 MG ORAL TABS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 15.08.2023
- Impfdatum
- 23.12.2022
- Beginn
- 30.07.2023
- Tage bis Beginn
- 219,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bradycardia
COVID-19
Hypotension
Syncope
Symptomtext
Hospitalization for syncope, COVID-19, bradycardia and hypotension on dates 7/30/2023-8/2/2023. Treated with dexamethasone, baricitinib, Remdesivir, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- ketorolac, lisinopril, atorvastatin, nut (Unspecified), shellfish, morphine, codeine
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 15.06.2023
- Impfdatum
- 23.11.2022
- Beginn
- 26.11.2022
- Tage bis Beginn
- 3,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Deep vein thrombosis
Symptomtext
ACUTE DVT OF LEFT POPLITEAL VEIN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 07.06.2023
- Impfdatum
- 03.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 19,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Deep vein thrombosis
Symptom recurrence
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN ACUTE DVT OF RIGHT POPLITEAL VEIN 12/17/2022, 2/25/2023, 1/14/2023, 2/20/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 19.05.2023
- Impfdatum
- 19.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Arteriogram carotid normal
Cardiac function test normal
Computerised tomogram head abnormal
Hypoaesthesia
Hypoaesthesia oral
Lacunar stroke
Magnetic resonance imaging head abnormal
Paraesthesia
Paraesthesia oral
Peroneal nerve palsy
Thalamic infarction
Symptomtext
On October 26,, 2022, I had symptoms of numbness & tingling in my right hand and above my lip (right side only). Symptoms were mild. Late evening I also had those symptoms plus a slight drop in right foot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lacunar stroke
- Hospital-Tage
- 1,0
- Labordaten
- CT on October 27, 2022 at Emergency Room in hospital showed a small hypodensity in L internal capsule area close to thalamus. Diagnosis - Lacunar Stoke of undetermined age. MRI on October 28, 2022 at Hospital - subacute evolving small left thalmic perforating artery distribution infarction. Angiogram performed on May 10, 2023 at the hospital showed no restriction in blood flow and no stenosis in carotid arteries Cardiac work-up since the stroke has been unremarkable.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 22.02.2023
- Impfdatum
- 22.11.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 37,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Blood test
Chest X-ray abnormal
Chest discomfort
Chest pain
Chills
Computerised tomogram thorax abnormal
Dyspnoea
Fatigue
Injection site pain
Lung opacity
Migraine
Pain in jaw
Pulmonary function test abnormal
Pulmonary thrombosis
Pyrexia
Toothache
Tremor
Symptomtext
Started developing left arm pain at the injection site. Later that evening started developing severe chills and shaking, fever and a Migraine. 2 hours later started developing jaw pain, fatigue and a fever. Next day had 102 fever and severe migraine headache, and took Sumatriptan. Started having chest pain and pressure 2 days after vaccine, and took Tylenol with Codeine with Sumatriptan. Called RN on COVID-19 Hotline and was told that deep chest pain was a symptom of COVID-19 vaccine, however if the pain changes to sharp go to the ER, never needed to because pain wasn't sharp. Next day had a 101.4 fever with chills with headache, fatigue, pain in jaw, teeth and chest pain with shortness of breath. Shortness of breath was steadily getting stronger. One month later went to ER was having severe chest pain on my right side and was admitted to the hospital for 11 days. Was given Heparin, then changed to Eliquis and put on oxygen. Given a CT Scan, Chest X-ray and bloodwork. CT scan showed that I had Pulmonary Blood clots in both lungs. When discharged was Oxygen, using 5 liters per minute. Home health was provided for 2 weeks. Had Occupational Therapy and Physical Therapy. Went back to my doctor and had a Pulmonary Function test and was able to decrease Oxygen intake to 2 liters per minute. Currently taking Eliquis and smaller amounts of Oxygen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary thrombosis
- Hospital-Tage
- 11,0
- Labordaten
- 12DEC29 CT Scan - Pulmonary Blood clots; Chest X-ray - Bibasilar Reticular Opacities.
- Aktuelle Erkrankungen
- Foot Pain Plantar Talntar Safiitis; Tidialis Posterior Tendinitis.
- Vorgeschichte
- Alpha-Antirantityrtsin; Cirrhosis of the Liver; COPD; Bronchiectasis; Chronic Hypocemic Respiratory Failure; Complex Sleep Apnea; Nocturnal Hypoxenia; Perfial Limb Movement; Bilatderal Peripherail Muscle Spasms; Chronic Migraines; Stenosis with Radicuphehy; Lumbar Fusion; IBS; Ulcerativecolitis; Hiatalhernia; GERD; Systemic Lupus Erytheatosus; Sjogren's Syndrome; Depression; ADHD; PTSD; Insomnia; Rosacea; Acne; Hyperlipidenia; Chronic Sinusitis; Vasomotor Rhinitis; Enviromental Allergies; Bilateral Kidney Stones; Orthostatic Hydotension; Renal Insufficiency; Hydronephrosis; Cataracts both eyes; Intraocular Lens Implant.
- Andere Medikamente
- Sereventdiskus; Albuterol Sulphate; Ropinirol; Tivanidine; Verapamil ER; Aimovig Autoinjector; Sumatritan; Tylenol with Codeine; Onabotulinumtoxin, injection every 6 weeks; Mesalamine Delayed Release; Folic Acid; Omeprazole DR; Tramadol as
- Allergien
- Penicillin; Cefazolin; Cethradine; Adhesive tape; Celebrex; Fulfasalazine; Cigarettes; Cats, Dust Mites
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 17.02.2023
- Impfdatum
- 20.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Computerised tomogram
Cough
Diarrhoea
Dry mouth
Headache
Loss of consciousness
Migraine
Nausea
Pain
Pain in extremity
Symptomtext
I experienced soreness all over my body, headaches, nausea, coughing, dry mouth, migraines, diarrhea, sharp stabbing pain in my left arm, back pain and I also passed out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- CT Scan
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Alprazolam
- Allergien
- Nuts
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 06.02.2023
- 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: unbekannt
Erholt: nein
Cognitive disorder
Confusional state
Gait disturbance
Hypophagia
Partial seizures
Symptomtext
focal seizure, confusion, couldn't eat drink after, cognitive issues, walking issues
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Partial seizures
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- fibromyalgia
- Andere Medikamente
- multi vitamin, levothyroxine, prevastatin,
- Allergien
- lyrica, statin
- Vorherige Impfungen
- Influenza
- Staat
- SD
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 26.01.2023
- Impfdatum
- 25.01.2023
- Beginn
- 26.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram cerebral abnormal
Atelectasis
Cerebral small vessel ischaemic disease
Chest X-ray abnormal
Endotracheal intubation
Hiatus hernia
Hypercapnia
Intensive care
Lung opacity
Mental status changes
Seizure
Unresponsive to stimuli
Symptomtext
The patient was found unresponsive in shelter and reportedly had witnessed seizure activity. He was intubated for altered mental status with hypercarbia and admitted to ICU.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- -
- Labordaten
- 1/26/23 CTA head: Periventricular and subcortical white matter hypodensities are noted, while nonspecific these are favored to represent mild chronic microvascular ischemic disease. 1/26 CXR: Interval intubation with tip of the endotracheal tube about 5.5 cm above the carina. An enteric tube is looped within a hiatal hernia posterior to the left heart. Streaky opacities in the left lower lobe along the border of the hiatal hernia consistent with atelectasis. No acute airspace consolidation. No large pleural effusion. No pneumothorax. The cardiac silhouette is normal in size.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hx chronic alcohol use. Hx Hepatitis C with prior treatment, HTN
- Andere Medikamente
- Iron and prilosec.
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 18.01.2023
- Impfdatum
- 18.01.2023
- Beginn
- 18.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysarthria
Facial paralysis
Feeling abnormal
Hypoaesthesia
Symptomtext
Patient came to the pharmacy about 6pm stating that he felt a little funny after his vaccination and that his right side felt numb. He was slurring his words and the right side of his face appeared to be drooping. I suggested we call an ambulance but he refused. The manager took him to call his wife to go to the emergency room.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Facial paralysis
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 18.01.2023
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood glucose abnormal
Computerised tomogram
Headache
Magnetic resonance imaging
SARS-CoV-2 test
Scan
Thrombosis
Visual field defect
Visual impairment
Symptomtext
Plavix for clots; Loss ability to put to see the lines on road; Peripheral vision impacted; Blood sugar 439; Headache; This is a spontaneous report received from contactable reporter(s) (Other 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 12Dec2022 at 15:15 as dose 4 (booster), single (Lot number: GJ6739) at the age of 62 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Diabetes" (unspecified if ongoing); "hypertension" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing). Concomitant medication(s) included: METFORMIN; VALSARTAN; OZEMPIC. Vaccination history included: Covid-19 vaccine (Dose 1/ Dose 2, Primary immunization series completed, 'Manufacturer unknown'), for COVID-19 immunization; Covid-19 vaccine (Dose 3, 'Manufacturer unknown'), for COVID-19 immunization. The following information was reported: BLOOD GLUCOSE ABNORMAL (hospitalization) with onset 12Dec2022, outcome "recovering", described as "Blood sugar 439"; HEADACHE (hospitalization) with onset 12Dec2022, outcome "recovering"; VISUAL IMPAIRMENT (hospitalization) with onset 12Dec2022, outcome "recovering", described as "Loss ability to put to see the lines on road"; VISUAL FIELD DEFECT (hospitalization) with onset 12Dec2022, outcome "recovering", described as "Peripheral vision impacted"; THROMBOSIS (hospitalization, medically significant), outcome "unknown", described as "Plavix for clots". The patient was hospitalized for thrombosis, visual impairment, visual field defect, blood glucose abnormal, headache (hospitalization duration: 1 day(s)). The events "plavix for clots", "loss ability to put to see the lines on road", "peripheral vision impacted", "blood sugar 439" and "headache" required physician office visit and emergency room visit. The patient underwent the following laboratory tests and procedures: Blood glucose abnormal: 439, notes: Blood sugar 439; Computerised tomogram: Unknown Results; Magnetic resonance imaging: Unknown Results; SARS-CoV-2 test: NO, notes: If covid tested post vaccination: No; Scan: Unknown Results. Therapeutic measures were taken as a result of thrombosis, visual impairment, visual field defect, headache. Clinical course: Report about covid treatment yes, Reporter type patient, No other vaccine in four weeks, Dose received more than 3, Loss ability to put to see the lines on road Peripheral vision impacted Driving was dangerous could not understand how to park Could not understand how to put on my pants or shoes on Dec19-21. Headache right after Blood sugar 439. AE resulted in doctor or other healthcare professional office/clinic visit, Emergency room/department or urgent care, Hospitalization. No days hospitalization 1, If treatment AE yes, If covid prior vaccination yes, If covid tested post vaccination no.; Sender's Comments: Based on the available information in the case, the causal association between the events THROMBOSIS, VISUAL IMPAIRMENT, VISUAL FIELD DEFECT, BLOOD GLUCOSE ABNORMAL, HEADACHE and the suspect drug BNT162B2 cannot be excluded. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- 1,0
- Labordaten
- Test Name: Blood sugar; Result Unstructured Data: Test Result:439; Comments: Blood sugar 439; Test Name: CAT; Result Unstructured Data: Test Result:Unknown Results; Test Name: MRI; Result Unstructured Data: Test Result:Unknown Results; Test Name: covid tested; Result Unstructured Data: Test Result:NO; Comments: If covid tested post vaccination: No; Test Name: Scan; Result Unstructured Data: Test Result:Unknown Results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Diabetes; High cholesterol; Hypertension
- Andere Medikamente
- METFORMIN; VALSARTAN; OZEMPIC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 17.01.2023
- Impfdatum
- 29.10.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 4,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cerebellar stroke
Ischaemic stroke
Magnetic resonance imaging
Symptomtext
Ischemic stroke in the cerebellar region
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebellar stroke
- Hospital-Tage
- -
- Labordaten
- MRI 11/3/2022
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- Stage 4 anal cancer
- Andere Medikamente
- Eliquis, L-Thyroxine, Ramipril, Metoprolol
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 13.01.2023
- Impfdatum
- 13.10.2022
- Beginn
- 16.10.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Agnosia
Anticoagulant therapy
Atrial fibrillation
Carotid artery thrombosis
Cerebral thrombosis
Ischaemic stroke
Laboratory test
Speech disorder
Surgery
Symptomtext
Patient experienced an ischemic stroke per spouse. Stated this happened 3 days after receiving pfizer bivalent injection. It was the 4th shot he has received, prior were all moderna covid 19 shots. Patient had two surgeries for the brain clot. One was to clear out the carotid artery brain clot, and then a second one that required an incision to clear the carotid out again for the patient. He went into afib as well at some point in time, and is now on therapy for that, but can have one of two elective surgeries to come off of the blood thinner he is required to take for controlled afib currently. Time course started at 9:30pm on 10/16/22 where the local fire department/rescue squad transported him to hospital, and then on 10/17/22 he was transferred to different hospital where he stayed from 10/17/22 to 10/27/22, then progressed to a rehab clinic where he stayed until 11/4/22. He is learning to recognize things again currently, speak more fluently, but is continuing to have ongoing issues from it that could take 6 months to a year to finely tune more, but will never more than likely be 100% again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Carotid artery thrombosis
- Hospital-Tage
- 20,0
- Labordaten
- Not sure of the tests and labs he had, do not have hospital records.
- Aktuelle Erkrankungen
- nothing one month prior or at time of vaccination
- Vorgeschichte
- lung fibrosis
- Andere Medikamente
- toprol xl, lipitor, gabapentin, singulair, paxil, flomax, vitamin b12
- Allergien
- no known allergies to anything
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 20.12.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Amnesia
Dizziness
Fall
Gait disturbance
Head injury
Syncope
Symptomtext
patient received both vaccinations in one sitting at the pharmacy; after injections, patient stated that she felt fine and went to sit with her parents in the post-vaccine waiting area; she started to feel dizzy and began to sway back and forth; she then fell back in her seat and hit her head; her parents turned her on her side making sure she was not having a seizure; she awoke a few seconds later stating she did not remember the fainting spell; EMTs were called
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- no medications being taken per patient's father
- Allergien
- peanuts; peanut oil
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 20.12.2022
- Impfdatum
- 20.12.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Symptomtext
after the 3rd injection the customer stated that she felt lightheaded and dizzy, then she passed out. Pharmacist kept her from falling to the floor and hitting her head, checked a pulse and she had a pulse. She came to momentarily and started talking saying she felt like she had taken a nap. After a few minutes she stood up and was able to walk out of the store. She let pharmacist know she has a history of seizures and that she has passed out with vaccines before and was really nervous for these ones.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- diabetes, hx of seizures
- Andere Medikamente
- na
- Allergien
- ceclor
- Vorherige Impfungen
- history of seizures
- Staat
- MN
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 18.12.2022
- Impfdatum
- 14.12.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Confusional state
Dizziness
Fatigue
Head injury
Injection site pain
Lethargy
Loss of consciousness
Syncope
Unresponsive to stimuli
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fainting / Unresponsive-Severe, Systemic: Weakness-Severe, Additional Details: Patient lost consciousness and hit her forehead during the 15 min wait time. Pharmacist aided and helped patient control her movements. Gave her ice pack to apply on forehead. Offered to call 911 for emergency but patient declined. Monitored patient until she regain strength and was able to answer questions about her name, date, where she is, what her plans were. Called patient 30 min later to follow-up to make sure she was okay at her hair appointment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 12.12.2022
- Impfdatum
- 11.11.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Activated partial thromboplastin time normal
Angiogram
Angiogram normal
Anticoagulant therapy
Arthralgia
Blood creatinine normal
Blood test normal
Deep vein thrombosis
Differential white blood cell count normal
Dyspnoea
Full blood count normal
Glomerular filtration rate normal
Heart rate increased
International normalised ratio normal
Metabolic function test
Metabolic function test normal
Oxygen saturation decreased
Prothrombin time normal
Symptomtext
On 11/14/2022, I woke up around 01:30 in the morning with some pain in my left knee. It was significant at the time. I took two TYLENOL and put a heating pad on my leg. I woke up around an hour later and the pain had become much more intense, and nothing would give any relief. I woke my husband up and we went to the local emergency room. I was diagnosed there with a deep vein thrombosis and have been prescribed ELIQUIS for treatment. On 11/18/2022, I had some increasing shortness of breath and low oxygen saturation. I monitored that over the weekend. On Monday, I had an elevated heart rate and shortness of breath. I was given a CT angiogram but that was returned negative. Since then, shortness of breath has been improving and my elevated heart rate is not as severe. I will follow up with hematology later this week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- 14NOV2022 Ultrasound, Deep Vein Thrombosis diagnosed; blood work, nothing abnormal found; Estimated GFR, nothing abnormal found; Creatinine, nothing abnormal found; Basic Metabolic Panel, nothing abnormal found; CBC with differential, nothing abnormal found; PTINR, nothing abnormal found; APTT, nothing abnormal found; 21NOV2022 CT Angiogram negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic back pain; Seasonal allergies
- Andere Medikamente
- Vitamin D; atorvastatin; estradiol; MYRBETRIQ; ALLEGRA; biotin vitamin; albuterol; SYMBICORT
- Allergien
- Quinolones; NSAID pain reliever
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 18.11.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest X-ray
Superficial vein thrombosis
Ultrasound Doppler abnormal
Symptomtext
I was diagnosed with a superficial thrombophlebitis. I need to keep leg elevated above heart, don' sit for long periods of time, take NSAIDS apply heated compress. Should resolve with time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Superficial vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Chest xray and ultrasound of the veins and arteries of my right leg.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin, macrodantin, sulfa
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 02.12.2022
- Impfdatum
- 18.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Cardiac monitoring
Confusional state
Dizziness
Lethargy
Paraesthesia
Presyncope
Symptomtext
Two days after vaccine felt dizzy, confused and felt tingling in fingers and toes and almost fainted, had to be helped home; Went to Dr. and had complete blood tests drawn, everything came back normal; Went to Cardiologist and given a heart monitor to wear; Haven't received results yet. Still feels lethargic since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- Blood panel drawn negative; Heart monitor, no results yet.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High blood pressure; Bradycardia.
- Andere Medikamente
- Amlodipine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 29.11.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Head injury
Syncope
Symptomtext
SYNCOPE, FAINTED AND HIT HEAD ON POLE, SMALL CUT ON SIDE OF FOREHEAD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 21.11.2022
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- 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
Patient passed out while sitting in chair, after receiving vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- Unknown, new patient to us
- Vorgeschichte
- Unknown, new patient to us
- Andere Medikamente
- Unknown, new patient to us
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 21.11.2022
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fall
Loss of consciousness
Symptomtext
Patient had vaccine while sitting in a chair. He stood up and seemed okay as he watched his dad get vaccine. But then he passed out and fell down.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown, new patient to us
- Vorgeschichte
- unknown, new patient to us
- Andere Medikamente
- unknown, new patient to us
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 20.11.2022
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Seizure
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Severe, Systemic: Seizure-Severe, Additional Details: Pt seized for about 3 minutes after administration of vaccination. No history of seizures. EMS called.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AS
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 18.11.2022
- Impfdatum
- 08.11.2022
- Beginn
- 12.11.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bell's palsy
Dry eye
Eye irritation
Facial paralysis
Headache
Neck pain
Symptomtext
Headache and neck pain beginning on 11/12/22, followed by droopiness of left eye on 11/15/22 and dry eye burning sensation. Progressive droopiness of left eyelid and paralysis on left side of face; droopy mouth on the left side. When I called the Healthcare for an appointment, the nurse recommended going to the emergency room and said that the symptoms could be related to a stroke. The subsequent diagnosis is Bell's Palsy. In researching, the onset coincides with getting the Covid booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- The diagnosis was based on the symptoms, medical history and physical examination.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure, pre-diabetic
- Andere Medikamente
- Norvasc, Lipitor, Jardiance
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 17.11.2022
- Impfdatum
- 16.11.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Dizziness
Loss of consciousness
Symptomtext
passed out after getting pfizer bival and fluarix vaccines. stomach upset and lightheaded. patient then informed that this has happened before. called 911 and gave water observed until ambulance arrived. they took blood pressure and questioned. pt refused to go to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- blood pressure and questioning from ambulance service
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- bipolar, rodiculopathy
- Andere Medikamente
- -
- Allergien
- none listed
- Vorherige Impfungen
- pt stated that she has passed out before with vaccination. unknown dates or vaccinations
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 22.10.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Blood test
Dyspnoea
Electrocardiogram
Pulmonary thrombosis
Symptomtext
After a couple of week of being short of breath, I started monitoring my heart rate and my blood oxygen levels, on 11/11/2022 my oxygen level was staying between 82-96 and my pulse rate I could not get under 100 beats per minute. So I went tot he nearest emergency room, I had extensive blood work done, EKG, and the Dr. came in and advised that I had multiple blood clots in both of my lungs. I was admitted in the hospital where I underwent heparin therapy. I stopped the therapy on Sunday 11/13/2022 and they put me ELIQUIS, and I was discharged from the hospital at that time. I am now home recovering, my heart rate has come down, but I am still short of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary thrombosis
- Hospital-Tage
- -
- Labordaten
- EKG 11/11/2022, blood work 11/11/2022, CT scan of lungs 11/22/2022, blood clots in both lungs.
- Aktuelle Erkrankungen
- COVID-19 09/19/2022 tested positive
- Vorgeschichte
- None
- Andere Medikamente
- Aspirin; citalopram; docusate sodium
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 27.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bell's palsy
Facial paralysis
Hypoaesthesia
Paraesthesia
Symptomtext
Left sided facial tingling and drooping as Bell's Palsy. Started 10/28/2022 after vaccination was seen and treated in ER followed up with PCP. Treated with Prednisone 20 mg 3 tablets daily for 7 days and Valtrex 1g three times daily for 7 days. Still has numbness and tingling in face.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- No knows illnesses within 30 days
- Vorgeschichte
- S/P Gastric Bypass, pernicious anemia, anxiety, depression, osteopenia
- Andere Medikamente
- Venlafaxine 75 mg and 150mg once daily, Cyanocobalamin 1000mg/mL 1 mL once a month, ferrous sulfate 325(65 Fe) 1 tablet daily, imodium a-d every 4 hours as needed.
- Allergien
- No known drug allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 14.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fall
Head injury
Loss of consciousness
Swelling
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Additional Details: Pt was sitting during observation period got dizzy and blacked out. She fell off of the chair and we helped her back up and gave her candy, water, and continued to observe her for another 20 minutes. She stated she got a bump on her head and gave her an ice pack to decrease swelling. I called her a day later to make sure she was fine and she said she is ok.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 17.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Loss of consciousness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Systemic: Weakness-Mild, Additional Details: While injection is taking place, patient was reported to have a very brief loss of consciousness not longer than 10 seconds. Patient was able to regain consiousness on her own while Immunizer was holding her from falling. Patient was observed from any further escalation of condition. Pharmacist on duty immediately assessed situation and assisted the patient and Immunizer until the area is well ventilated for the patient. Patient recovered and was able to stand up and walk/drive home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure increased
Dizziness
Flushing
Headache
Hyperhidrosis
Hypotension
Loss of consciousness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Headache-Medium, Systemic: Hypotension-Medium, Additional Details: Patient received 2 vaccines in the left arm IM. She stood up too fast and started feeling light headed. She passed out for a few seconds. I immediately called for the PA to assist as her friend and myself pulled her up after fainting. She told me afterwards that she tends to faint after receiving vaccinations. She regained consciousiness. Her BP was checked by the PA 3 different times and increased over 45 minutes to 1 hour. She rested with her feet raised and felt better after drinking water.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Confusional state
Dizziness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 17.10.2022
- Impfdatum
- 30.09.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alanine aminotransferase normal
Albumin globulin ratio
Anion gap
Aspartate aminotransferase normal
Basophil count normal
Basophil percentage
Bell's palsy
Blood albumin normal
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium normal
Blood chloride normal
Blood creatinine normal
Blood glucose normal
Blood potassium normal
Blood sodium normal
Blood urea nitrogen/creatinine ratio
Blood urea normal
Symptomtext
On the Evening of October 1, 2022 , following the two vaccines described above (on September 30, 2022) I noticed left sided changes in muscle contractions in my neck without pain. That progressed to mild left sided paralysis in my face on Monday October 3rd, 2022. I wen to the emergency room and was diagnosed with mild Bell's Palsy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- ED Provider Notes at 10/3/2022 3:17 PM MEDICAL CENTER ED Provider Note Patient 54 y.o. male History Chief Complaint Patient presents with ? Facial Droop Patient noticed facial droop since saturday. Patient had flu vaccine and covid booster on friday. HPI 54-year-old male presents with facial droop. He reports he noticed that approximately 36 hours ago. He underwent the quadrivalent COVID booster on Friday as well as the annual flu vaccination. Reports he noticed symptoms on Sunday where his platysma was not as visible on the left side and he also had a slight left-sided facial droop. Denies any speech changes. No numbness or weakness. No physical pain. No ear pain or sore throat. No apparent fevers. No similar prior episodes in the past. No apparent modifying features. Past Medical History: Diagnosis Date ? Asthma, persistent controlled 8/29/2014 ? Chronic seasonal allergic rhinitis due to pollen 11/22/2017 ? Dermatitis 10/26/2016 Non specific, blanching 2015 ? HTN.. 3/11/2021 ? Hyperlipidemia LDL goal < 100 12/23/2014 ? Hypertension ? Obesity (BMI 30.0-34.9) 8/16/2017 ? Obstructive sleep apnea syndrome 5/23/2018 Past Surgical History: Procedure Laterality Date ? Exploratory laparotomy as infant, look for undescended testicle ? Vasectomy 2007 Social History Substance and Sexual Activity Alcohol Use Yes ? Alcohol/week: 0.0 standard drinks Comment: 3 x week scotch and water Social History Tobacco Use Smoking Status Never Smoker Smokeless Tobacco Never Used E-Cigarettes ? Vaping Use Never User ? Start Date ? Cartridges/Day ? Quit Date Social History Substance and Sexual Activity Drug Use Not Currently Allergies Allergen Reactions ? Mushroom Diarrhea Discharge Medication List as of 10/3/2022 3:51 PM CONTINUE these medications which have NOT CHANGED Details albuterol sulfate (PROVENTIL) 2.5 mg/3 mL nebulizer solution Take 3 mLs (2.5 mg dose) by nebulization every 4 (four) hours as needed for Wheezing., Starting Sat 12/11/2021, Normal albuterol sulfate HFA (PROVENTIL,VENTOLIN,PROAIR) 108 (90 Base) MCG/ACT inhaler Inhale two puffs into the lungs every 6 (six) hours as needed., Starting Sat 12/11/2021, Normal cetirizine (ZYRTEC) 10 MG tablet Take 10 mg by mouth daily., Until Discontinued, Historical Med fluticasone-salmeterol (ADVAIR DISKUS) 250-50 mcg/dose AEPB inhalation powder Inhale 1 puff into the lungs 2 (two) times daily., Historical Med hydrochlorothiazide (HYDRODIURIL) 12.5 mg tablet TAKE 1 TABLET BY MOUTH EVERY DAY, Normal losartan potassium (COZAAR) 50 mg tablet TAKE ONE TABLET BY MOUTH DAILY., Normal metformin (GLUCOPHAGE) 1000 MG tablet Take one tablet (1,000 mg dose) by mouth 2 (two) times a day with meals. Last refill until appointment 10/13/22, Starting Tue 9/6/2022, Normal mometasone (NASONEX) 50 MCG/ACT nasal spray SPRAY 2 SPRAYS INTO EACH NOSTRIL EVERY DAY, Normal montelukast (SINGULAIR) 10 MG tablet TAKE 1 TABLET BY MOUTH EVERY DAY, Normal simvastatin (ZOCOR) 40 mg tablet TAKE 1 TABLET BY MOUTH EVERYDAY AT BEDTIME, Normal triamcinolone (ARISTOCORT,KENALOG) 0.5% cream APPLY TO AFFECTED AREA 3 TIMES A DAY FOR 30 DAYS, Normal Review of Systems Review of Systems Constitutional: Negative for fever. HENT: Negative for sore throat. Eyes: Negative for pain. Respiratory: Negative for shortness of breath. Cardiovascular: Negative for chest pain. Gastrointestinal: Negative for abdominal pain and vomiting. Genitourinary: Negative for dysuria. Musculoskeletal: Negative for back pain. Skin: Negative for rash. Neurological: Negative for headaches. Psychiatric/Behavioral: Negative for suicidal ideas. All other systems reviewed and are negative. Physical Exam ED Triage Vitals [10/03/22 1448] BP (!) 176/87 Heart Rate 84 Resp 18 SpO2 100 % Temp 98.2 ?F (36.8 ?C) Physical Exam Nursing note and vitals reviewed. Constitutional: He does not appear distressed and no respiratory distress. Well appearing HENT: Head: Atraumatic. Eyes: Conjunctivae are normal. Neck: No nuchal rigidity. Cardiovascular: Normal rate and intact distal pulses. Pulmonary/Chest: No respiratory distress. Respiratory effort normal and breath sounds normal. Abdominal: Soft. There is no abdominal tenderness. Musculoskeletal: No obvious deformity noted to extremities. Neurological: He is alert. Decreased nasolabial fold on the left. Platysma is somewhat less evident on the left when patient flexes his jaw. He has decreased movement of the left forehead as compared to the right. He has normal strength and sensation all 4 extremities. Other than above cranial nerves II through XII are intact. Normal speech. No ataxia. Normal gait. Skin: Skin is warm. Skin is dry. Psychiatric: He has a normal mood and affect. ED Course Lab results: CBC AND DIFFERENTIAL - Abnormal Result Value WBC 7.6 RBC 5.14 HGB 15.3 HCT 45.1 MCV 88 MCH 29.8 MCHC 33.9 Plt Ct 234 RDW SD 47.1 (*) MPV 10.6 NRBC% 0.0 NRBC 0.000 NEUTROPHIL % 57.5 LYMPHOCYTE % 29.8 MONOCYTE % 8.4 Eosinophil % 3.2 BASOPHIL % 0.7 IG% 0.400 ABSOLUTE NEUTROPHIL COUNT 4.38 ABSOLUTE LYMPHOCYTE COUNT 2.3 MONO ABSOLUTE 0.6 EOS ABSOLUTE 0.2 BASO ABSOLUTE 0.1 IG ABSOLUTE 0.030 COMPREHENSIVE METABOLIC PANEL - Abnormal Na 142 Potassium 4.0 Cl 102 CO2 27 AGAP 13 Glucose 102 (*) BUN 14 Creatinine 0.83 Ca 10.1 ALK PHOS 41 T Bili 0.30 Total Protein 7.8 Alb 5.0 GLOBULIN 2.8 ALBUMIN/GLOBULIN RATIO 1.8 BUN/CREAT RATIO 16.9 ALT 27 AST 29 eGFR 104 Comment: Normal GFR (glomerular filtration rate) > 60 mL/min/1.73 meters squared, < 60 may include impaired kidney function. Calculation based on the Chronic Kidney Disease Epidemiology Collaboration (CK-EPI)equation refit without adjustment for race. Imaging: No data to display ECG: ECG Results None Pre-Sedation Procedures MDM Coding Provider Communication Overall clinical picture appears consistent Bell's palsy likely secondary to recent vaccination. The symptoms appear to be relatively mild at this time. We discussed facial exercises in addition to Artificial tearsAnd eye taping at night although he is still able to close his eye at this time. Will give prescriptions as below with recommendation to have him follow-up closely with his primary care physician for reassessment. Patient notably hypertensive but no signs of endorgan damage at this time. Discharge Medication List as of 10/3/2022 3:51 PM START taking these medications Details predniSONE (DELTASONE) 20 mg tablet Take three tablets (60 mg dose) by mouth daily for 7 days., Starting Mon 10/3/2022, Until Mon 10/10/2022, Normal valacyclovir (VALTREX) 1000 mg tablet Take one tablet (1,000 mg dose) by mouth 3 (three) times a day for 7 days., Starting Mon 10/3/2022, Until Mon 10/10/2022, Normal Discharge Medication List as of 10/3/2022 3:51 PM Discharge Medication List as of 10/3/2022 3:51 PM Clinical Impression Final diagnoses: Bell's palsy Elevated blood pressure reading ED Disposition ED Disposition Discharge Condition Stable Comment -- Follow-up Information MD Specialty: Internal Medicine Go to Emergency Department. Specialty: Emergency Medicine Comments: If symptoms worsen Contact information: Electronically signed by: MD 10/04/22 1510 Discharge Instructions at 10/3/2022 3:47 PM
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, metabolic syndrome, sleep apnea, hyperlipidemia, asthma
- Andere Medikamente
- Simvastatin, HCTZ, Losartan, Metformin, Wixela, Nasonex, Montelukast, cetirizine
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 15.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild, Additional Details: patient passed out for about a minute or 2 after receiving a flu and a covid booster vaccines. paramedics were called in and checked vitals. all vitals were normal. patient left home with parent afterwards
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Clonus
Dizziness
Loss of consciousness
Syncope
Symptomtext
on getting 2nd shot she said "i think i'm going to pass out" Pt has syncopal event after immunizations today. Patient was seated for immz. She vocalized she felt like she was going to pass out. Mom and I layed her down. She has a mild clonus and was "out" for about 10 seconds. Pt woke spontaneously and was not post ictal. Pt was kept supine for 5 minutes during history portion of appointment and gradually head of table was raised to 90 degrees. Pt was completely recovered in 10 minutes and was advised to tell staff in future she fainted after a shot in past
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 09.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye movement disorder
Loss of consciousness
Seizure
Syncope
Tremor
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Severe, Systemic: Seizure-Severe, Additional Details: Patient was unconcious and shaking violently after reciving both vaccines. Eyes rolled behind their head and started shaking. Patient unresponsive for 10 seconds but felt okay afterwards and was concious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 08.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Hyperhidrosis
Nausea
Presyncope
Vomiting
Symptomtext
Approximately 25 minutes after the vaccine, I start to experience intense diaphoresis and nausea that lead to several bouts of vomiting. I then vasovagaled and had 1 bout of non-bloody diarrhea. The symptoms self resolved in about 20 minutes following vomiting, having diarrhea, and lying on the floor. I?m a primary care physician, and this happened while I was at work, so I knew what was occurring and did not seek a higher level of care. I also have never vasovagaled following vaccines previously, although I used to with venipunctures as a child.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Generalized anxiety Seasonal allergies
- Andere Medikamente
- Venlafaxine 75mg daily Zyrtec 10mg daily
- Allergien
- Almonds - mouth swelling, nausea, vomiting (prior anaphylaxis) Apples - mouth swelling, nausea, vomiting
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 07.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Loss of consciousness
Musculoskeletal disorder
Pallor
Symptomtext
Patient was sitting in the chair and a minute or two after administering both vaccines he slouched over and passed out. He had a difficult time coming around and he was pale and white. The ambulance was called and patient was taken to the hospital to be checked out. He was OK and coherent by time the ambulance came.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- None listen on intake sheet
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 28.09.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Syncope
Symptomtext
Pt fainted just after receiving the vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 22.12.2023
- Impfdatum
- 21.10.2022
- Beginn
- 24.10.2023
- Tage bis Beginn
- 368,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Blood creatinine increased
Brain natriuretic peptide increased
COVID-19
Chest X-ray abnormal
Echocardiogram normal
Ejection fraction normal
Fall
Limb injury
Lung opacity
Orthostatic hypotension
SARS-CoV-2 test positive
Wound haemorrhage
Symptomtext
Patient is a 88 y.o. male with history of a fib on Eliquis, SSS with pacemaker HTN, T2DM admitted to the hospital on 10/24/2023 for recent falls at home & chronic weakness. Patient had overall negative trauma workup, however was found to have hazy opacifications on CXR with elevated BNP. Echo was done which showed stable HF not in exacerbation. Additionally was found to be COVID-19 positive with positive orthostatics. During his hospital course he remained normotensive while holding all of his home antihypertensives. Falls were likely related to hypotension secondary to COVID19 infection and antihypertensive medications. During the hospital stay he was seen by PT/OT who recommended SNF which patient declined and was made aware of risks associated. He was offered remdesivir for his COVID infection and patient declined. Action Items to be Addressed After Discharge 1) COVID19 Infection - follow up symptoms, supportive 2) HTN/HF - Consider restarting home BP medications; BMP 3) Orthostatic Hypotension; follow up PT 4) Atrial Fibrillation - Adjusted eliquis 5mg BID to eliquis 2.5mg BID given age/renal function Discharge Diagnosis and Associated Hospital Course Generalized weakness Recurrent falls COVID-19 infection Orthostatic hypotension HTN Patient had unwitnessed falls at home, one directly after standing. CXR (10/24) with mild hazy opacification L lung. Found to have orthostatic hypotension, likely culprit for falls. Seen by PT/OT recommending SNF, family declined, discussed risks and patient and family understood. Family declined COVID19 treatment with remdesivir. Considered outpatient PT while patient is only in area for roughly approximately 2 weeks before returning to home. Referral placed. -Consider restarting and/or decreasing home antihypertensives, repeat BMP -Follow up PT Chronic HFpEF BNP elevated 2,560. Increased from 734 in 2019. Likely related to infection vs less likely heart failure exacerbation. -Echo (10/26) with EF 59, LVH normal wall function. RSVP 46 CKD AKI, unable to rule in nor ruled out Consistent with baseline. Unclear etiology as diabetes is well controlled. - On admission Cr 1.82, 1.4 on discharge Chronic Afib On home Eliquis 5 mg BID - held on admission due to bleeding from wounds on upper extremity - Restarted Eliquis dose reduced to 2.5mg BID given CKD and age Anemia of Chronic Disease - Stable Appears consistent with baseline. Chronic Thrombocytopenia - Stable Consistent with baseline NIDT2DM Diet-controlled - Continue SSI while admitted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Orthostatic hypotension
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 21.12.2023
- Impfdatum
- 08.12.2022
- Beginn
- 23.05.2023
- Tage bis Beginn
- 166,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
Angiogram abnormal
Asthenia
Bacteraemia
Brain fog
COVID-19
COVID-19 pneumonia
Computerised tomogram abdomen
Cough
Dizziness
Fatigue
Hypoxia
Pneumonia
Pyrexia
Retching
SARS-CoV-2 test positive
Streptococcal bacteraemia
Symptomtext
Reported Symptoms: 10000081:ABDOMINAL PAIN; 10013573:DIZZINESS; 10016558:FEVER; 10047862:WEAKNESS; 10052104:DRY HEAVES; Narrative: Patient admitted for COVID-19 pneumonia, bacteremia. Required treatment with Remdesivir, dexamethasone, zinc, vitamin C and ceftriaxone, metronidazole for pneumonia and bacteremia. Was discharged after 11 day hospital stay in improved condition. Other Relevant HX: Patient is a 75-year-old male with a past medical history that includes hypertension, COPD, hepatitis C, gastrointestinal stromal tumor status post imatinib and partial gastrectomy, pneumonia. Presented to emergency department with complaints of 1 week of dizziness, cough, fatigue, "brain fog." Tested positive for COVID-19 in the ED and was noted to have hypoxemia during ambulation. CTA abdomen also showed findings concerning for left lower lobe pneumonia. Pt admitted for patient admitted for COVID-19 and hypoxemia. Pt was treated with Remdesivir and dexamethasone, zinc, vitamin C. Also received ceftriaxone and metronidazole for community acquired bacterial pneumonia/Streptococcus constellatus bacteremia. Other: weakness, abd pan, dryheaves
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- -
- Labordaten
- COVID-19 (Cephid) positive 5/22/23
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- -
- Geschlecht
- M
- Eingang
- 01.11.2023
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Maternal exposure during pregnancy
Supraventricular tachycardia
Symptomtext
Neonatal SVT; Vaccinated twice during pregnancy/third trimester; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the parent. A fetus male patient was exposed to bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), transplacental, administration details for the mother: on 17Nov2022 at 18:00 as dose 5 (booster), single (Lot number: GJ6739), in left arm for covid-19 immunisation. The mother of the patient was 31 years old at the time of vaccination. The mother's relevant medical history included: "Hashimotos" (unspecified if ongoing). Date of last menstrual period of the mother: 01Apr2022. The mother was 32 weeks pregnant at the time of exposure to bnt162b2, bnt162b2 omi ba.4-5. The mother was 33 weeks pregnant at the event onset. The mother is expected to deliver a baby(s) on 06Jan2023. Concomitant medication(s) included: TDAP taken for immunisation, on 21Oct2022 as dose 1, single; LEVOTHYROXINE; BABY ASPIRIN; PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]. The mother's vaccination history included: moderna (Dose 4 (Booster), Single, Prev dose lot number=051B22A, Prev dose vaccine location=Left arm), administration date: 06Aug2022, for COVID-19 immunization; moderna (Dose 3 (Booster), Single, Prev dose lot number=058H21A, Prev dose vaccine location=Left arm), administration date: 22Nov2021, for COVID-19 immunization; bnt162b2 (Dose 2, Single, Prev dose lot number=EW0173, Prev dose vaccine location=Left arm), administration date: 30Apr2021, for COVID-19 immunization; bnt162b2 (Dose 1, Single, Prev dose lot number=EW0158, Prev dose vaccine location=Left arm), administration date: 09Apr2021, for COVID-19 immunization. The following information was reported: MATERNAL EXPOSURE DURING PREGNANCY (hospitalization, congenital anomaly, life threatening) with onset 17Nov2022 at 18:00, outcome "recovering", described as "Vaccinated twice during pregnancy/third trimester"; SUPRAVENTRICULAR TACHYCARDIA (hospitalization, congenital anomaly, life threatening) with onset 14Jan2023 at 13:00, outcome "recovering", described as "Neonatal SVT". The patient was hospitalized for maternal exposure during pregnancy, supraventricular tachycardia (hospitalization duration: 3 day(s)). It was also reported that Event results in Prolongation of existing hospitalization (vaccine received during existing hospitalization, as reported). The events "vaccinated twice during pregnancy/third trimester" and "neonatal svt" required physician office visit and emergency room visit. Therapeutic measures were taken as a result of supraventricular tachycardia, treatment included Adenosine, propranolol. Clinical courses: Vaccinated twice during pregnancy including: Pfizer bivalent. Son experienced SVT minutesnafter delivery with no past family history of arrhythmia and no SVT documents: during pregnancy NSTs. Neonatal SVT occurred with a rate of about 300 bpm, converted with adenosine, immediately after birth on (withheld) and then again a few weeks later at home. Son was placed on propranolol and was well controlled. Medicine was tapered and stopped around 6-7 months of age. Son is 9 months, and his SVT is believed to be in remission at this time. Risk may be vastly: outweighed by benefits. The reporter is not an anti-vaxxer, but does wonder if her vaccination during pregnancy whether based on fact of vaccination or timing of its administration: during third trimester, contributed to neonatal SVT of her son. She hopes this will be looked into given known incidence of cardiac impacts of COVID-19 and known incidence of myocarditis, particularly in males. myocarditis, particularly in males.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300351826 same reporter, different patient and AE(baby/mother);US-PFIZER INC-202300351759 same reporter, different patient and AE(baby/mother);
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Supraventricular tachycardia
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- LEVOTHYROXINE; BABY ASPIRIN; PRENATAL VITAMINS [MINERALS NOS;VITAMINS NOS]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 17.10.2023
- Impfdatum
- 21.10.2022
- Beginn
- 29.10.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
ACTH stimulation test normal
Abdominal distension
Abdominal pain upper
Antinuclear antibody negative
Aphasia
Areflexia
Arthralgia
Arthropod bite
Asthenia
Autoantibody negative
Autonomic nervous system imbalance
Axillary pain
Balance disorder
Bedridden
Biopsy skin abnormal
Blindness transient
Blood calcium normal
Blood creatine phosphokinase normal
Symptomtext
10/29/2022- heart palpitations, irregular pounding, and fluttering 10/31/2022- high BP and HR, feeling faint with moments of vision going black and like I might pass out 11/4/2022- mild to moderate sore throat began and continues intermittently, varying in severity. 11/7/2022- full body debilitating weakness, varies in severity and comes and goes, sometimes lasts for an hour, sometimes half a day or more -During weakness attacks, which have lessened in frequency- head pressure, neck stiffness/soreness, pressure behind eyes, cannot keep eyes open or head up, blurry vision (began 11/14/2022), headaches, heart pulsing through my body, irregular heartbeat detected, extreme weakness/fatigue throughout whole body, high blood pressure 11/7/2022- quick sharp headaches, intermittent and varying in severity, often short and sharp pains, occasionally longer 11/9/2022- trouble standing, walking, brain fog. -standing- I can?t stand for very long without losing strength in my muscles, or starting to sway and lose balance and coordination, with pain or shakiness in hips and knees, I often have to hold on to things. I do not drink alcohol anymore, but it often feels as if I am drunk. -walking- has become increasingly difficult, unsteady, and often feel I am in slow motion, with heavy lower legs. This lack of strength, slow motion, and pain in knees and hips happens after about 15-30 minutes of walking normally. -brain fog- started noticing confusion, memory problems 11/11/2022- joint aches and stiffness, mostly ankles and wrists 11/12/2022- muscle weakness, extreme soreness, and fatigue, fatigued and sore from doing very little 11/12/2022- very stiff, sore, and painful back of neck 11/12/2022- intense head pressure, mostly front of face, temples, and behind eye, but also in the back of head. Has since increased in severity, often feels like bones are moving or expanding 11/14/2022- vision changes, blurry vision with head pressure, white flashes and black streaks in peripheral vision 11/14/2022- slow moving, feeling as though I have to consciously coordinate movements 11/20/2022- neck is unsteady sitting up at times, weakness, can?t keep it upright, occasional tremors 11/20/2022- numb and tingly left side of face, jaw to cheek bone, intermittent 11/21/2022- tremors/twitching in left thumb 11/25/2022- heavy legs have worsened, tight and feel weighted as soon as I get out of bed or stand up, often from mid-calf down, sometimes from knees down. There is a distinct line where I can feel the tightness/numbness down to my toes. Lasts all day, gets better laying down and with rest 11/28/2022- cognitive issues worsening, feels like early dementia at times. I forget the topic of conversations while they are happening, cannot find the right words, forget peoples names, forget where dishes go while putting them away, finding items in weird places that they should not be and no recall of how they got there. 11/30/2022- sensitivity to light, varies in severity, headlights at night are very bothersome 12/2/2022- sinus pressure, severe at times, no fluid or drainage, no congestion or stuffiness, just intense pressure. I can often hear and feel things popping and crackling around up there all day. Increased in severity, feels as though my brain or bones are expanding 12/2/2022- top row of teeth ache at times, in varying severity, seems to correlate with increase in head and sinus pressure 12/28/2022- circulation issues worsening, always have been a cold person with cold hands and feet, but around this time started to notice swollen red toes, sometimes entire white feet, bulging veins in my feet that itched to start, no longer itch 1/3/2023- noticed minor cuts on feet where my skin rubbed off between toes, red and raw, but never felt it happen, and don?t feel any pain or discomfort. These cuts took over 2 months to heal. 1/15/2023- very dry mouth, increased thirst and urination, clear urine at times. No amount of water satiates, immediately thirsty again after drinking water. This happens intermittently. 1/15/2023- severe sore throat at times, seems to be in one spot 1/15/2023- occasional pain/lumpy feeling in front of neck 1/23/2023- bone pain from knees to toes, bone pain in skull, noticing space between front teeth is getting larger, confirmed by dentist on 1/30/2023, who also noticed very dry mouth 2/7/2023- full leg numbness/loss of feeling after driving 2 hours for an appointment, inability to walk normally, legs bent, could not straighten, feet shuffled across the floor 2/8/2023- ability to walk worsened, full body tremors when trying to stay still, very little balance, no control. 2/11/2023- different type of weakness, felt like I could fall asleep at any moment or pass out, no strength in my body, also happened 2/12/2023 2/14/2023- BP higher and higher, reached 165/125 2/15/2023- different type of headache, not the pressure I was having before, Tylenol helps (Started propranolol 2/14/23 and within 24 hours the intense head pressure, body tremors, and inability to sit upright or keep my head upright have all majorly improved. BP also normalized.) 2/16/2023- very dry skin on face, bumpy and scaly, no amount of lotion helps, comes and goes 3/1/2023- bulging veins in hands in addition to feet, intermittent 3/1/2023- joint pain is worse, constant. Kness are especially worse, feel like jelly, hyperextending while standing or trying to walk 3/9/2023- tightness/numbness in lower legs is now entire legs, and random places in my body. Sometimes symmetrical, sometimes not 3/13/2023- ability to walk worse and worse (3/15/22- diagnosed with Small Fiber Neuropathy) 3/23/2023- purchased a cane to help me walk, which helped a lot 3/27/2023- bedridden now, can?t lift my head or body, can barely make it to the bathroom 4/3/2023- noticing cold patches of skin in different places, but I am not cold internally. noticed low body temperature around this time, 96-97 degrees 4/6/2023- leaking urine, not a steady daily leak, it happens randomly, panty liner works 4/7/2023- GI issues worsening, constipation and diarrhea on and off, Dr noticed very quiet bowel sounds with a stethoscope 4/27/2023- heat intolerance, cannot withstand temperatures above 65 it seems, can?t be in the sun for more than a few minutes- rashes and redness anywhere the sun touched my skin, nausea, very disoriented, dizzy, skin hot to the touch long after coming inside, moody, very irritable, more pain everywhere, and it took over 24 hours to cool down 4/30/2023- noticing I am becoming short of breath from doing nothing, happens intermittently. Also noticed I run out of breath suddenly while trying to talk. 5/1/2023- cannot walk at all without elbow crutches, cannot stand without support, cannot sit for longer than 20-30 minutes or my face starts to go numb. Purchased a shower chair, cannot stand long enough to shower. 5/12/2023- mottled skin all over legs 5/20/2023- difficulty swallowing at times, intermittent, feels like a severe sore throat but there is no soreness, just takes more effort to swallow 5/21/2023- skin discoloration in calves and sometimes toes, on and off, purplish color, worse behind my knees 5/25/2023- noticing increased stiffness in wrists, hands, and fingers 5/25/2023- rapid muscle fatigue getting worse and worse, in legs but also my entire body after any use at all. Arms going dead from brushing hair, teeth, washing hair. This has been happening since early on but have noticed an increase in severity recently. 7/7/2023- GI issues worsening, nausea, regurgitation within an hour of eating, constipation/diarrhea, bloating, stomach pain (diagnosed with Autonomic Dysfunction)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 10/29/2022- symptoms began 8 days after deer tick bite and pfizer covid booster, which were both on 10/21/2022. Was started on doxycycline 10/22/2022 for tick bite, could not tolerate, but switched and continued with ceptin for 3 weeks, otherwise no other changes to prompt symptoms 10/31/2022- first ER visit #1 after 3 days of palpations, high BP, and pain in left armpit- calcium 10.5, leukocytes 13.3, mean corpuscular hemoglobin 36.5, neutrophils absolute 9.13, BP 157/125, possible arrythmia in EKG, prescribed ZIO patch for 2 days which was normal, ER docs did not have much to say 11/6/2022- ER visit #2- EKG said- Sinus rhythm Abnormal R-wave progression, early transition Compared to previous ECG, no significant change 11/7/2022- positive Epstein Barr nuclear antigen AB IGG, positive Epstein Barr viral capsid AB IGG, immature granulocyte absolute 0.07, negative Lyme/tick panel 11/18/2022- ER visit #3, I was told by Neurology to go and have a STAT lumbar puncture and MRI of spine before my upcoming appt. on 11/23/22, but was ultimately denied these tests at the ER by the Neurologist on duty saying, ?this is not an emergency?. An abnormal heart rate detected during triage, EKG said- Sinus rhythm Consider left atrial enlargement Compared to previous ECG, no significant change. The docs here said I have weakness, but not concerned for Guilliane-Barre 11/21/2022- leukocytes 10.5, platelet count 446, neutrophils absolute 7.71, glucose 129, calcium 10.2, CRP 35.8, ESR 37 11/23/2033- 2/1/2023 Neurology appointment with Dr., physical neurological exam showed proximal weakness, tests ordered- Creatine kinase (normal), myasthenia gravis (normal), ANA (normal), Rheumatoid factor (normal), protein electrophoresis serum and urine (normal), Sjogren's (normal) celiac disease (normal). In this doctor's notes, without mentioning her thoughts to me, and with no psychological exam, or even asking how I was doing, she wrote that this could be ?psychogenic?. No tests had been done at that time for her to exclude all possibilities. I saw her until 2/1/2023, only through online messages, where she continued to tell me that ?mind-body connection was a negative one?. When the bloodwork came back normal, she decided that was good enough and concluded that there was nothing neurological going. I was denied further testing when asked. She then ended our relationship ?wishing me the best quality of life achievable?. I asked her for a second opinion, but she declined. When I was inevitably referred back to her office for further evaluation, I asked her for guidance on who to see next, she did not reply. (recommended to stop Cabergoline entirely by both endo and neurology on 11/25/2022 in case it was the cause of symptoms-it wasn?t) 12/1/2022- ER visit #4- Heart rate 111, BP 134/91, platelet count 441, erythrocyte distribution width low at 11.8%, calcium 10.2, ESR and CRP normal. At this visit after no physical or psychological exam I was told by the attending doctor to ?consider the possibility that this is all a psychological problem?. I left in tears. 12/19/2022- MRI brain- 3mm pituitary growth, suspected cystic microprolactinoma. MRI cervical spine- C4-5: There is trace vertebral and uncovertebral spur. There is no focal disc herniation or significant spinal stenosis C5-6: There is asymmetric osteophyte disc complex posterior-laterally on the left. There is slight encroachment on the left lateral recess and left neural exit foramen. There is no focal nerve root impingement. 12/22/2022- prolactin 38.6ng (taken without stopping biotin supplement) 1/30/2023- prolactin 48ng, platelet count 445, ESR 26, Reproductive hormones, all collected 3 weeks into ?cycle?- FSH- 2.6, LH 3.4, progesterone 0.29, estrogen 5.4 2/6/2023- leukocytes 10.3, platelet count 468, neutrophils percent 88, lymphocytes percent 10, monocytes percent 2, neutrophils absolute 9.01, monocytes absolute 0.17, lymphocytes absolute 1.01, iron binding capacity 387 2/12/2023- ER visit #5- glucose 108, calcium 10.4, BP-159/110, Neurological exam by Dr. positive for weakness and numbness, but tried to diagnose me with Functional Neurological Disorder (Neurologist #3 who thinks I?m crazy) 2/14-2023- EMG neurology test, Dr.- normal. BP-157/107. Dr. was the first neurologist to do further testing, and suggested the skin biopsy test 2/14/2023- Endocrinology visit, Dr.- BP-152/95 2/14-2023- started Propranolol in the afternoon (that I had to start myself on), and 24 hours later saw major improvements in BP, no pressure in my head, no body tremors, I can stand for a bit longer, and I have been able to keep my head up without needing support. 2/16/2023- Cardiology appointment, Dr., BP normal, agreed with propranolol use at 20mg 2X/day 2/22/2023- Echocardiogram performed- normal. Ultrasound of arteries in legs- also normal 3/1/2023- Skin biopsy for small nerve neuropathy by neurology- results in 11 business days 3/9/2023- MRI of lumbar spine- normal 3/14/2023- Vit B1-115 (normal), Vit B6- 7 (very low normal) 3/14/2023- Tested for all paraneoplastic autoantibodies- all normal 3/15/2023- Skin biopsy results- Positive for ?significant? Small Fiber Neuropathy. Right thigh-9.1 (Low normal) Right calf- 2.46 (significantly reduced epidermal nerve fiber density) 3/20/2023- Pain Specialists- Dr. Exam found no reflexes in ankles. Thought possibly fibromyalgia, prescribed 4.5mg of naltrexone, did not know much about small fiber neuropathy 3/22/2023- Medical Center- Vascular surgery, normal ultrasound of veins 3/23/2023- Cane purchased 3/29/2023- Nortriptyline prescribed by PNP, started at 50mg before bed 4/10/2023- Bloodwork for PCP- Compliment C4- 45.2 (high), CRP cardiac- 7.9 (high), prolactin 41.6 (high), normal SED rate 4/24/2023- Endocrinology Dr., ACTH stim test- all normal 5/5/2023- Pain specialists- Dr.- increased naltrexone to 4.5mg 2X/day, thinks my case is beyond his scope of expertise and requires more urgent action 5/5/2023- Forearm crutches prescribed by PCP 5/12/2023- Leukocytes- 10.9 H, neutrophils absolute- 8.29 H 5/30/2023- Dr thinks all symptoms and diagnoses from vaccine on 10/21/22 6/22/2023- autonomic testing abnormal- diagnosed with POTS, as well as abnormal QSART, blood circulation
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hyperprolactinemia
- Andere Medikamente
- cabergoline, adderall, womens daily vitamin, probiotic
- Allergien
- sulfa, doxycycline, penicillin
- Vorherige Impfungen
- Flu Vaccine in 2020- rash at injection site
- Staat
- FL
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 15.09.2023
- Impfdatum
- 28.11.2022
- Beginn
- 08.09.2023
- Tage bis Beginn
- 284,0
- Dosis
- 5
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Anaemia
COVID-19 pneumonia
End stage renal disease
Hypertension
Superinfection
Troponin increased
Type 2 diabetes mellitus
Symptomtext
Hospitalization for COVID-19 viral pneumonia with superimposed bacterial pneumonia, suspected AKI on CKD stage V/ESRD, elevated troponin, anemia, Type 2 Diabetes, hypertension on dates 9/8/23- 9/13/23. Treated with dexamethasone, vitamin C 1,000 mg PO daily, vitamin D 25 mcg PO daily, zinc 50 mg PO daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- tetanus and diptheria toxoids
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 15.08.2023
- Impfdatum
- 29.11.2022
- Beginn
- 11.01.2023
- Tage bis Beginn
- 43,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injected limb mobility decreased
Pain in extremity
Periarthritis
Symptomtext
PT RECEIVED 3 VACCINES ON 11/29/2022 FLUARIX ,PFIZER AND SHINGRIX . Patient came to the pharmacy on 01/11/2023 and complained about left arm/shoulder pain that started after getting the vaccines (she received Fluarix and Shingrix on left arm) and limited mobility of her arm. Pt reported using a medrol dose pack that helped her with pain. The patient also stated that she submitted VAERS on her own. 08102023 patients again came to the pharmacy and reported continuing side effects of shoulder and arm pain. She has been to different providers and received cortisone shots that helped her for a bit but the pain is back. Her MRI was denied by insurance. Her doctor also suspects frozen shoulders. Patient might pay out
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- -
- Andere Medikamente
- N/A
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 03.07.2023
- Impfdatum
- 03.07.2023
- Beginn
- 03.07.2023
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Hypoaesthesia
Paraesthesia
Peripheral coldness
Symptomtext
Upon receiving covid vaccine client started feeling dizzy upon exiting clinic door to sit down in the lobby for 15 min wait. but did notify nurse. At 9:25am clients spouse seeked help from nurse due to client still feeling dizzy. Nurse took client in a wheelchair into a clinic room. Client mentioned breakfast had been consumed and had drank water prior to coming to todays appointment. Two nurses assisted client in laying down on exam room table. Placed a pillow under clients head. Blood pressure was 124/68. Client also complained of still feeling numbness and tingling in both hands. After 5min. assisted client in sitting up on exam table. Gave client a cup of water. By that time client said numbness & tingling was very minimum and only sensation she had was cold hands. Client mentioned dizziness had improved and was mild. Client felt comfortable in walking out to go home and rest. Clients spouse & nurse walked client to car with no difficulties. Client was in clinic room 10 min total.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Omeprazole
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 29.06.2023
- Impfdatum
- 05.10.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 27,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angiogram
Arthralgia
Asthenia
Back pain
CSF red blood cell count positive
Chest discomfort
Chest pain
Decreased appetite
Dizziness
Dyspnoea
Dyspnoea exertional
Electromyogram
Facet joint syndrome
Fatigue
Headache
Hypoaesthesia
Imaging procedure abnormal
Intervertebral disc degeneration
Symptomtext
Neurological: Bilateral ascending LE numbness, increasing weakness, fatigue, tremors, dizziness, breathing difficulties when exercising, muscle cramping, heaviness off upper and lower extremities
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Current symptoms Left Piriformis Syndrome Numbness and tingling sensation up both thighs and both forearms; heavy legs Frequent headaches / neck pain Waves of extreme fatigue Lightheadedness/feeling faint Short of breath sensation, heavy sighs Sensation of chest pressure or pain thru to the back (comes and goes) Muscle weakness; hand tremors; frequent muscle cramps (L foot) Ice cold hands and feet Weight loss; loss of appetite Severe joint pain - mostly hands (fibromyalgia? March 1/osteoarthritis) Raynauds syndrome Night sweats Occasional low back pain (Severe degenerative disc disease L4-5, S1 - NSAIDs; muscle relaxers; PT as needed) Tests for Diagnosis 1-5-2023 - MRI Lumbar Spine WO W Contrast L5-S1: Significant disc narrowing w/degeneration, disc bulge and spondylitis; L4-L5: Significant disc narrowing w/degeneration, broad disc bulge and spondylitis (eccentric R laterally) 2-21-2023 - EMG and NCS - Extensive Labwork - Lyme Disease PCR - 3-17-2023 - Radiation Oncology Consultation with Dr for suspected Paraneoplastic Syndrome 3-28-2023 - MRI Thoracic Spine WO W Contrast 3-31-2023 - MRI Cervical Spine WO W Contrast C5-C6: Asymmetric circumferential most pronounced posterolaterally to R side; C6-C7: Moderate circumferential disc bulge with bilateral facet arthropathy. 3-31-2023 - MRI Brain WO W Contrast 4-11-2023 - FL Lumbar Puncture Diagnostic Abnormal result - RBC count of 34 in CSF (Standard range 0-10) - Traumatic Tap?? But there was no decrease of RBC?s from tubes 1 and 4 which is not indicative of a traumatic tap which generally would show a decrease of RBCs in later tubes. 4-20-2023 - MRA Chest WO W Contrast Further testing to consider, possible dedicated spinal angiography? Other than noted above, there were no remarkable findings in determining cause of symptoms, which continue to get worse. Looking to rule out vascular as cause: PAD; Popliteal Artery Entrapment Syndrome; Chronic Exertional Compartment Syndrome; other?
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis; IBS
- Andere Medikamente
- Ibuprofen pm
- Allergien
- Lactose intolerance
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 23.05.2023
- Impfdatum
- 18.05.2023
- Beginn
- 19.05.2023
- Tage bis Beginn
- 1,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Condition aggravated
Deafness
Tinnitus
Symptomtext
I have had tinnitus for many years, however 24 hours after receiving my 2nd bivalent Covid vaccine the tinnitus became significantly worse. I have an appointment coming up with an audiologist for testing and treatment and also an appointment with my ent provider. I also have a hearing loss that occurred. A couple months after receiving my 3rd Covid vaccine. I have filed a separate Baer?s report temporary Vader?s e-report number 967105
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Will be having updated hearing test date tbd
- Aktuelle Erkrankungen
- Glaucoma COPD
- Vorgeschichte
- COPD glaucoma
- Andere Medikamente
- Celebrex, montelukist, losartan
- Allergien
- Bactrim
- Vorherige Impfungen
- Covid #3 10/012021 Pfizer previously reported
- Staat
- TX
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 05.05.2023
- Impfdatum
- 27.12.2022
- Beginn
- 19.03.2023
- Tage bis Beginn
- 82,0
- Dosis
- 4
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Dyspnoea
HIV test negative
Myalgia
Nasopharyngitis
Rhinorrhoea
SARS-CoV-2 test negative
Sneezing
Streptococcus test negative
Symptomtext
On 03/19/2023 I went to the beach it was cold and windy , temperature of 65. After coming back from the beach I had a runny nose and I was sneezing.. It continued till 2 weeks. On 04/01/2023 I started having a severe cough, runny nose, muscles ache, shortness of breath and hard to breath. 04/09/2023 I had a appointment at the pharmacy for COVID-19 test was negative, strep test was negative. They told me that it was a common cold and prescribed me with a cough medication Brompheniramine- Pseudoephedrine- DM ( 5 days) . On 04/15/2023 I had runny nose , cough, and muscles aches. On 04/21/2023 I went to get more tests done such at STD and HIV which was negative. On 04/22/2023 I still have a dry cough, and muscles aches. On 04/23/2023 I went to the doctor again I was prescribed with inhaler, Antibiotics ( Azithromycin) 6 days and cough syrup ( Benzonatate). After finishing the medication my symptoms reduced but it didn't go away completely. I try to use Vicks but it lost it's effectiveness on me. This is something new that I am experience. In total I went to the doctors like 3 times. I will be scheduling another appointment for the severe cough which I still have . I don't even have fever so no one is sure what is going on with me.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 09APR2023 COVID-19 Test- Negative; 09APR2023 STREP Test- Negative; 21APR2023 STD- Test- negative; 21APR2023 HIV Test- Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 01.05.2023
- Impfdatum
- 09.11.2022
- Beginn
- 02.01.2023
- Tage bis Beginn
- 54,0
- Dosis
- 6
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Atrial fibrillation
Cardiac stress test
Cardioversion
Cryotherapy
Dyspnoea
Echocardiogram
Echocardiogram abnormal
Heart rate increased
Influenza
Influenza virus test positive
SARS-CoV-2 test negative
Symptomtext
On 1/2/2023, at approximately 12:00 AM, I was lying in bed, and I felt very short of breath. I spent the next six hours sitting at a 90-degree angle, dozing intermittently. At 6:00 AM, I drove myself to the ER. At the ER, I spent approximately six hours. I was tested for COVID-19 and influenza. I tested negative for COVID-19 and positive for influenza. I was given SOLUMEDROL intravenously and a breathing treatment with a steroid whose name I don't know. I was then discharged and given a prescription for prednisone at 40 mg, which I was to take daily for seven days. I followed up with my PCP two weeks later, at which time it was discovered that I was in atrial fibrillation. The PCP began treating me with digoxin and CARDIZEM. At this point, my heartrate was 140, and they wanted to get it down. I returned to the PCP five days later. I was then given XARELTO, LASIX, and potassium. I was then referred to a cardiologist, whom I was scheduled to see in four months' time. Two weeks later, I ended up back in the ER on 2/13/2023, because I had shortness of breath. The ER gave me a referral to another cardiologist, whom I saw on 2/14/2023. The cardiologist discontinued the CARDIZEM and digoxin and prescribed me metoprolol. On 2/15/2023, I underwent a stress test and an echocardiogram. The results indicated that I did not have heart disease and that I just had atrial fibrillation. I then saw the cardiologist again on 3/9/2023. We discussed why I had atrial fibrillation, since I had never had cardiac trouble before. He explained that there were now all sorts of new bugs, such as COVID-19, nowadays and that their long-term effects aren't really known at this point. He then said that he would not be surprised if the atrial fibrillation had been brought on by the influenza. On 3/28/2023, I underwent an esophageal echocardiogram and two cardioversions. I then went into regular sinus rhythm, which lasted until 4/1/2023. I woke up at about 3:00 AM with shortness of breath, and I knew that I had atrial fibrillation again. I spoke to the cardiologist, who wanted to schedule me for an ablation, but I would not be able to undergo the ablation until September or October 2023. I then began calling other medical centers and found out about a cardiologist in another city. I spoke with this cardiologist, who informed that there are two types of ablation: cryoablation and radio frequency ablation. I saw the cardiologist on 4/13/2023, and he scheduled me to undergo a cryoablation on 4/26/2023. I underwent the ablation as scheduled, and I have been in normal sinus rhythm ever since. He also started me on two new medications: flecainide and colchicine. I am scheduled for a follow-up appointment with the cardiologist on 5/9/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 02JAN2023 COVID-19 and Influenza tests, negative for COVID-19, positive for Influenza; 15FEB2023 Stress Test, Echocardiogram, Atrial Fibrillation indicated, no heart disease detected
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism; Thrombocytosis; Chronic Bronchitis
- Andere Medikamente
- Levothyroxine; hydroxyurea; multivitamin; baby aspirin
- Allergien
- Penicillin; sulfa drugs
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 27.04.2023
- Impfdatum
- 26.10.2022
- Beginn
- 01.03.2023
- Tage bis Beginn
- 126,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac monitoring abnormal
Cardiac operation
Cardiac pacemaker insertion
Chest X-ray normal
Echocardiogram normal
Electrocardiogram normal
Palpitations
Symptomtext
I was feeling palpitations and I took my blood pressure and noticed my heartrate was in the 40's. So, I went to urgent care. I was recommended to a Cardiologist, and I finally got in to see one and they put a monitor on me and within four hours they called me and told me I needed to go to the emergency room. I ended up having to have a Pacemaker installed. I was in the hospital for four days total before being released after surgery.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- 4,0
- Labordaten
- APR2023 Echocardiogram, normal; APR2023 EKG, normal; APR2023 Chest X-Rays, normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Lisinopril; Hypothyroidism; Dry Eyes
- Andere Medikamente
- SYNTHROID; lisinopril; RESTASIS; aspirin; fluocinolone acetonide oil; ESTRING
- Allergien
- Sulfa; gluten; seasonal allergies; lilies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 25.04.2023
- Impfdatum
- 24.10.2022
- Beginn
- 26.02.2023
- Tage bis Beginn
- 125,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dyspnoea
Fatigue
Headache
Influenza virus test
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I was having a cough, sore throat, headache, shortness of breath, a low-grade fever. I took a home COVID-19 home test and it was positive. I went into a pharmacy and got a test, and it was positive as well. I reached out to my health care provider, and they put me on PAXLOVID and that did help. I was so fatigued and was napping everyday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test; COVID-19 PCR test; Influenza test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Celiac Disease; Hashimoto's; Osteopenia
- Andere Medikamente
- Rosuvastatin; estradiol; multivitamin; vitamin D3; calcium
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 25.04.2023
- Impfdatum
- 17.10.2022
- Beginn
- 01.02.2023
- Tage bis Beginn
- 107,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arrhythmia
Blood test normal
Cardiac monitoring abnormal
Chest X-ray normal
Electrocardiogram normal
Laboratory test normal
Palpitations
Symptomtext
I heart palpitations on and off. I went to the ER and they took a whole bunch of test and nothing came up. I wore heart monitor and nothing came up except for heart arrhythmia. I don't have the date of the tests . I still have heart palutations. I had the flu vaccine on the other other but I cannot remember which arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- Bloodwork, EKG ; Chest X-ray - Nothing
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Coronary Artery Disease since 2015
- Andere Medikamente
- Omeprazole ; Baby Aspirin ; Iron Supplement; Atorvastatin ; Losartan ; Magnesium; Vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- Shingles I had fever, body aches and chills
- Staat
- GA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 20.04.2023
- Impfdatum
- 17.10.2022
- Beginn
- 12.01.2023
- Tage bis Beginn
- 87,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chills
Cough
Dysphonia
Dyspnoea
Influenza like illness
Malaise
Productive cough
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I went to emergency clinic due to my COVID-19 symptoms. I took a home test and was positive 01/12/2023 for COVID-19. I developed chills and a low grade fever and had flu like symptoms. I developed a cough, and I could not breath, was so congestion, had phlegm. I was concerned it would go into my lungs. I saw a physician assistant in the emergency clinic 01/30/2023. I still have a bit of hoarseness at times but feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 12JAN2023 COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamins
- Allergien
- None
- Vorherige Impfungen
- COVID vaccine 1st and 2nd dose, chills and fever, felt horrible and also to the Shingles vaccine experienced chills and fever
- Staat
- FL
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 13.04.2023
- Impfdatum
- 07.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nasopharyngitis
Tremor
Symptomtext
I received the 5th dose and I started having something like a head cold. I went to see my doctor and I was given Ardizone and a that didn't help. The doctor had me come back in and had a cocktail of different medicines, FLONASE twice saline and brand name AIR and it took me two weeks to see improvements. I then started seeing tremors in my had and as time continued, I noticed it was a full body of tremor. I have some brain scans and other test scheduled. I don't know if these things are connected but it's been a rough 6 months. I took the other shots and had no issues this is just very weird to start having all these issues after the 5th dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Cancer, Diabetes; Hypertension
- Andere Medikamente
- CENTRUM SILVER 50 plus; ALA; quinapril; lisinopril; losartan; metformin; cancer AFINITOR; ezetimibe; insulin
- Allergien
- Lisinopril; gardinas
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 25.11.2022
- Beginn
- 21.03.2023
- Tage bis Beginn
- 116,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood magnesium decreased
Blood potassium decreased
Chest X-ray normal
Chest pain
Computerised tomogram thorax normal
Dyspnoea
Respiratory tract congestion
Symptomtext
In March I was in my friend's house and the AC was blowing at my back. Two days later, I had congested chest and hard to breath. My chest hurt . I spoke to pulmonologist' s nurse on the phone and was prescribed antibiotics Levaquin . After taking it for 3 to 4 days, there was no difference and they prescribed to another medication. I went to ER, I still want to see a doctor and did CAT scan to make sure I was better even if I was feeling better. They said that I may have had Pneumonia. I had it in the past and I know how it felt.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 4/3/23 CAT scan, Chest Xray - All Negative ; Blood work Low Magnesium and Potassium
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Amlodipine; Atorvastatin; Pantoprazole; Zolpidem
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 10.04.2023
- Impfdatum
- 10.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Dry mouth
Dyspnoea
Hypoacusis
Nasal disorder
Nasal operation
SARS-CoV-2 test negative
Sinonasal obstruction
Upper respiratory tract infection
Symptomtext
I had dry mouth, difficulty breathing, and long-term cough. I tested negative for COVID-19 several times. I went to the doctor and they gave me an inhaler which did not do anything. I got to the point to where I couldn't hear properly in my right ear. It was sinus blockage and I had to get surgery on my nose cavity so I could breathe better. This helped but I just got an infection in my nose, and I am still coughing and stuffy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 10/2022, COVID-19 test, negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Type 2 Diabetic; Heart Failure
- Andere Medikamente
- OZEMPIC; JARDIANCE; losartan; hydrochlorothiazide; metformin
- Allergien
- Cilantro; lisinopril
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 10.04.2023
- Impfdatum
- 07.10.2022
- Beginn
- 01.03.2023
- Tage bis Beginn
- 145,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Migraine
Symptomtext
I had migraines for a good amount of time post vaccination. I was not prescribed medication. I just took acetaminophen. I am still dealing with the migraines at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Anxiety
- Andere Medikamente
- PROZAC; MIRENA IUD
- Allergien
- Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 10.04.2023
- Impfdatum
- 08.10.2022
- Beginn
- 27.03.2023
- Tage bis Beginn
- 170,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypersomnia
Lethargy
Loss of personal independence in daily activities
Migraine
Nausea
SARS-CoV-2 test negative
Symptomtext
She had an intense migraine that lasted about a week, followed by another week of nausea. I contacted her doctor, and she was prescribed amoxicillin. They diagnosed her with a migraine and possible sinus infection. She is feeling better now. She is not completely better, but she is feeling better. Also, when she received this dose, she was sleeping more than usual and was very lethargic. She was off school for several days because she was unable to function.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- 31MAR2023 COVID-19 test negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 07.04.2023
- Impfdatum
- 01.10.2022
- Beginn
- 09.10.2022
- Tage bis Beginn
- 8,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Condition aggravated
Gait disturbance
General physical health deterioration
Inflammation
Osteoarthritis
Pain
Pain in extremity
Restless legs syndrome
Walking aid user
X-ray abnormal
Symptomtext
About a week after receiving my vaccine, I went to the doctor for hip pain. He noticed in my x-rays that I had severe osteoarthritis. After that, everything went downhill even further more. I started limping more and went to see to my ortho doctors. My restless leg syndrome flared up; I went from walking normally and freely to now having to use a walker for assistance for the last 3 or 4 months to get around due to severe pains I'll have shooting up my leg. I have an appointment with my ortho and neurologist soon for updates soon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- OCT2022 X-Ray, inflammation
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Bipolar 2; Osteoarthritis; Hypothyroidism
- Andere Medikamente
- Levothyroxine; omeprazole; LEXAPRO; LIPITOR; gabapentin; MIRAPEX
- Allergien
- Amoxicillin; LAMICTAL
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 06.04.2023
- Impfdatum
- 01.01.2023
- Beginn
- 19.02.2023
- Tage bis Beginn
- 49,0
- Dosis
- 5
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest X-ray abnormal
Dyspnoea
Malaise
SARS-CoV-2 test positive
Symptomtext
Patient is fully vaccinated, boosted, and up to date on COVID-19 vaccinations - last dose 1/4/2023. His onset of COVID-19 symptoms was on 2/19/2023 with shortness of breath. At the hospital on 2/19/2023, patient tested positive for COVID-19 and had an abnormal chest x-ray. He was admitted to the hospital on 2/19/2023. No treatment information was provided. 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
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 2/19/2023 - Positive COVID NAA test 2/19/2023; Abnormal chest x-ray.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Hypertension and cardiac disease.
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 30.03.2023
- Impfdatum
- 03.11.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 53,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Allergy test negative
Blood test normal
COVID-19
Chest X-ray normal
Condition aggravated
Cough
Diarrhoea
Differential white blood cell count normal
Dyspnoea
Eye disorder
Fatigue
Gastric disorder
Laboratory test normal
Loss of personal independence in daily activities
Nasal congestion
Pain
Post-acute COVID-19 syndrome
Pulmonary function test normal
Symptomtext
I had what I thought was an upper respiratory issue in October of 2022. I realize now that it was a case of COVID-19. I didn't realize that a faint pink line was still considered positive. I developed a cough at that time and that has lasted since then. I woke up around 05:00AM ET on 12/26/2022 and was feeling tired and achy. The symptoms continued on throughout the day and by the end of the day, it had hit me really hard. I tested bright pink positive, and the upper respiratory symptoms were worse this time as soon as it hit. I had stomach problems, fever, and severe nasal congestion. My coughing was still bad, but it did not get worse than it was in the fall. It was just harsh and did not seem to respond to any medication. I've been tested for allergy issues, pulmonary issues and other testing. This cough causes severe stomach issues and fatigue. I have continued taking anti-depressants and the occasional anti-anxiety pill because I've been locked in the house. I'm being treated with inhalers, but when it gets bad, nothing seems to help in any way. I just can't catch my breath. The stomach issues just come and go, and I will get sudden diarrhea. I am used to being outdoors and have a horse, but I haven't been able to get to the farm since the fall. I coughed so hard on Thanksgiving that it caused eye problems. This has been a devastating few months. My doctor believes it is long COVID-19 at this point. I've tested negative for everything else.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 09FEB2023 - Pulmonary Function Test - Nothing Abnormal; 01NOV2022 - Blood Work - Nothing Abnormal; Chest X-Rays - Nothing Abnormal; Automated Diff - Nothing Abnormal
- Aktuelle Erkrankungen
- Minor Case Of COVID-19
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Celebrex; Gabapentin; Lexapro; Vitamin D; Magnesium; Daily Vitamin; Flonase; Azelastine HCL
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 30.03.2023
- Impfdatum
- 28.09.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 64,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ankle fracture
Arthralgia
Fall
Mobility decreased
X-ray
Symptomtext
I had vaccination on 09/28/2022. 07/2022 I fell and broke my right ankle. I was off my foot till about 10/2022. In 12/2022 I started noticing my hip was aching at night more than usual. I attributed this to my body realigning itself as I was getting off the cane for walking. The left hip aches when I lie down and a tender spot. I did have X-rays on 03/17/2023. I have an appointment on 04/03/2023 to find out the results.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- X-rays 03/17/2023
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Hydrochlorothiazide; vitamin D; magnesium
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 23.03.2023
- Impfdatum
- 29.11.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Mobility decreased
Pain in extremity
X-ray
Symptomtext
can't lift arm, pain in arm, headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- xray
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 06.03.2023
- Impfdatum
- 01.12.2022
- Beginn
- 13.12.2022
- Tage bis Beginn
- 12,0
- Dosis
- 5
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Injected limb mobility decreased
Injection site hypoaesthesia
Injection site paraesthesia
Oropharyngeal pain
Pain
Paranasal sinus discomfort
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I tested positive for COVID-19 on 12/13/2022. I had sore throat, fatigue, body aches, sinus pressure, cough, and congestion. I contacted my doctor and was prescribed PAXLOVID. I also took TYLENOL, vitamin C, vitamin D, and zinc. I am still dealing with these symptoms currently. I also had numbness and tingling in my left arm at the injection site. It progressively got worse. I let my doctor know. I have not been able to use my arm as much as usual. I did some research, and it may have been human error. They might have stuck the needle in too far and did some nerve damage.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- 13DEC2022 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Osteoarthritis; Gastritis
- Andere Medikamente
- N/A
- Allergien
- ADVIL; BIAXIN; clarithromycin; IMITREX; PAXIL; CELEXA; WELLBUTRIN; sodium laurel sulfate; bees; latex; sanitizers; raw honey; walnuts; berries; corned beef
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 17.02.2023
- Impfdatum
- 13.12.2022
- Beginn
- 13.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood electrolytes normal
Chest X-ray normal
Chest discomfort
Chest pain
Full blood count normal
Hypoxia
Renal function test normal
Throat tightness
Troponin normal
Symptomtext
Tightness in the chest, chest pain, tightness in the throat, hypoxia. Two doses of IM epinephrine, fluids and diphenhydramine given. Patient transported to Emergency Department for work up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Chest Xray, troponins, electrolytes, blood counts, and kidney function all normal.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Heart palpitations, sciatica, GERD, seasonal allergies, menopause, urinary incontinence, osteopenia, hypertension, hyperlipidemia, osteoarthritis
- Andere Medikamente
- Amlodipine, estradiol, fluticasone, gabapentin, loratadine,
- Allergien
- Pencillins (anaphylactic)
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 06.02.2023
- Impfdatum
- 23.09.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 19,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthritis
Computerised tomogram abnormal
Condition aggravated
Fatigue
Inflammation
Lymphadenopathy
Sarcoidosis
Sinusitis
Symptomtext
I had a sinus infection, and I went to the doctor. They did a CAT scan and found swollen lymph nodes in my neck and chest. I was diagnosed with sarcoidosis. It also could be from my medication I am taking called SIMPONI. They are still trying to figure out how to treat this. I have inflammation, fatigue, and more arthritis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- CAT scan; Sarcoidosis, 10/25/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Underactive thyroid; Chronic Sinus Infection; Asthma; Colitis; Arthritis
- Andere Medikamente
- ADVAIR; ATROVENT; ELAVIL; ERRIN; FLONASE; INCRUSE; ORILISSA; rosuvastatin; SIMPONI; SYNTHROID; ZYRTEC
- Allergien
- AUGMENTIN; BENADRYL; BACTRIM; miconazole
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 06.02.2023
- Impfdatum
- 02.10.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 59,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthma
Chronic kidney disease
Hypertension
Obesity
Symptomtext
Diagnosis o Principal Problem: Severe asthma with acute exacerbation o CKD stage 4 secondary to hypertension (CMS/HCC) o Class 3 severe obesity due to excess calories with serious comorbidity and body mass index (BMI) of 40.0 to 44.9 in adult (CMS/HCC)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.02.2023
- Impfdatum
- 03.11.2022
- Beginn
- 08.01.2023
- Tage bis Beginn
- 66,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Cough
Decreased appetite
Ear pain
Gait inability
Headache
Nausea
Oropharyngeal pain
Pain
Pain in extremity
Paranasal sinus discomfort
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Tremor
Symptomtext
On 1/8/2023, it was very late at night, my hands were shaking very bad, I could not take a test. I had chills, no appetite, sore throat, earache, sinus pressure filled with mucus. I had a terrible headache and a lot of nausea, body aches, and a lingering and painful cough. I tested positive on the next day. I was sleeping in the extra bedroom, my left foot was having severe pain, I could not walk for 4 days. I would take ADVIL to relieve the pain. It was really extreme. I called my doctor and got prescribed PAXLOVID and promethazine. I also had a fever. My sense of smell was great, I still cough in the morning with congestion. I don't need to take my cough medicine until I go to bed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- 08JAN2023 COVID-19 positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism; GERD; Arthritis; IBS; High Blood Pressure
- Andere Medikamente
- Levothyroxine; metoprolol; NEXIUM; vitamin D; multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 29.11.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 29,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Bronchitis
COVID-19
Chest X-ray abnormal
Dyspnoea
Fatigue
Hypertension
Insomnia
Mechanical ventilation
Pain
Pain in extremity
Pyrexia
Restlessness
SARS-CoV-2 test positive
Symptomtext
On December 28, 2022, he was restless and unable to sleep. On the 29th he had a low-grade fever. He tested positive for COVID-19 on the 29th. The doctor prescribed him an anti-viral and took that for 5 days. He complained of pain in his legs and fatigue. He had body aches. In two weeks, he seemed to be feeling better. But then he began to complain of difficulty breathing. A month later he was still testing positive for COVID-19. He was admitted to the hospital on January 23, 2023, and was discharged on January 29th but returned to the hospital today, January 31st, because of shortness of breath and high blood pressure. He is still testing positive for COVID-19. He is on a ventilator via mouth and nose. They are treating him with antibiotics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 7,0
- Labordaten
- COVIDS-19, positive, December2022 and January2023; X-Ray chest, inflammation in bronchial;
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- ALS
- Andere Medikamente
- Lorazepam; Tylenol; Benadryl; Cyclobenzaprine
- Allergien
- Codeine; Kiwi
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 05.10.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 76,0
- 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
12/20/22 presents to ED for "shortness of breath". PMHx of "T2DM, HTN, oropharyngeal dysphagia, and chronic pain"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 12/20/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 12.01.2023
- Impfdatum
- 16.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 5,0
- Dosis
- 5
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Central venous catheterisation
Chills
Hypoxia
Malaise
Mental status changes
Nausea
Pyrexia
SARS-CoV-2 test positive
Sepsis
Spinal cord infection
Tachycardia
Symptomtext
ED 11/21/2022 with altered mental status and fever - recently seen for infection in his spinal cord, tx with IV antibiotics line for prolonged period of time, remains on oral antibiotics -Patient did receive Decadron given his oxygen requirement in the setting of being COVID-positive. Admit diagnoses: Sepsis - fever, tachycardia; resolved; Covid positive; Weakness, malaise; Hypoxia; Fever and tachycardia on admission, resolved with sepsis fluid bolus and acetaminophen. Suspect fever and tachycardia are due to COVID-19 infection (positive PCR today). Hospitalized again 12/8/2022 with chills/nausea. Submitter does not have access to full medical record. If additional information is needed, please contact hospital noted above.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- COVID-19 positive 11/21/2022.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Past Medical History: Diagnosis Date Alcohol dependence in remission; 7/12/2021 Alcohol withdrawal 7/12/2021; Clotting disorder 10/22/2021; Hyperlipidemia; Hypertension; Major depressive disorder with current active episode 10/22/2021; PTSD (post-traumatic stress disorder) 10/22/2021; Uncontrolled type 2 diabetes mellitus, without long-term current use of insulin 10/22/2021.
- Andere Medikamente
- Prior to Admission medications Acetaminophen (TYLENOL); Ammonium lactate; Ascorbic acid (VITAMIN C ORAL); Atorvastatin (LIPITOR); Buspirone (BUSPAR); Carvedilol (COREG); Chlorhexidine (PERIDEX); Clonidine HCL (CATAPRES); Duloxetine (CYMBALT
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 31.12.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Chills
Headache
Pain
Tremor
Symptomtext
Severe shaking, shivering and teeth chattering. Full body aches. Severe headache. Symptoms started approximately 16 hrs after receipt of dose. Shaking lasted around an hour. I was unable to get to a thermometer to check temp at the time. Several hours later I took Tylenol and checked temp which was 103.5 F. at that time. I alternated Tylenol and Motrin and temperature subsided in about 8 hours. Headache and body aches lasted another 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Collagen deficiency - joint hypermobility.
- Andere Medikamente
- Multivitamin, Additional Vitamin D supplement.
- Allergien
- Tylox, Vicodin, Nickel
- Vorherige Impfungen
- COVID Phizer BioNtech EL 9269 date 02/17/2021 - age 53, Severe shaking, body aches, headaches, temp reached 107.1
- Staat
- -
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Adjusted calcium
Alanine aminotransferase normal
Albumin globulin ratio
Angiogram abnormal
Angiogram pulmonary abnormal
Anion gap
Aspartate aminotransferase normal
Asthenia
Auscultation
Basophil count decreased
Basophil percentage decreased
Bilirubin urine
Blood albumin normal
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium decreased
Blood chloride increased
Blood creatinine normal
Symptomtext
Pt reported heart palpitations. Vitals: 220/112; 101,18 EMS Called @1320; Pt taken to ER IN ER: Pt was at covid vaccine clinic, 3 min after receiving vaccine, pt reports onset of continuous palpitations. Denies dizziness, SOB, N/V. C/o Right Rib pain for past few days. Hx of HTN. Patient is a 59 y.o. female who presents for evaluation of palpitations. Patient was at a vaccine clinic this afternoon, she had just received her COVID booster, when she began experience palpitations which has since improved and are now only intermittent. Staff took her blood pressure and found this to be elevated prompting EMS. Patient denies recent fevers/chills, illness/injury. At the time of interview no complaint for headache, change in vision, difficulty speaking, neck pain, chest pain, shortness of breath, back pain, abdominal pain, or new weakness/numbness/tingling to extremities. Pt describes left rib discomfort with palpation for the last few days (triage note not withstanding). 11/15 @14:37 36.6 ?C (97.9 ?F) 91 12 (!) 219/115 98 % Result Date: 11/15/2022 Narrative: Examination:XR CHEST 1 VIEW PORTABLE Indication:Hypertension Comparison:None FINDINGS: No infiltrate or effusion. Cardiac size is within normal limits. IMPRESSION: No evidence of pneumonia or edema. Finalized by MD at 11/15/2022 3:28 PM EKG: EKG interpretation EKG interpreted by myself -- Obtained at 1429 shows sinus, rate 92, no acute significant ST segment abnormalities, LABS: Labs Resulted Up to the Time of Admitted to the Floor CBC WITH DIFFERENTIAL - Abnormal Result Value Ref Range Status WBC 7.84 4.50 - 11.00 K/uL Final RBC 4.57 4.00 - 5.20 M/uL Final Hemoglobin 10.9 (*) 12.0 - 16.0 g/dL Final Hematocrit 36.2 36.0 - 46.0 % Final MCV 79.2 (*) 80.0 - 100.0 fL Final MCH 23.9 (*) 26.0 - 34.0 pg Final MCHC 30.1 (*) 31.0 - 37.0 g/dL Final RDW 14.3 11.5 - 14.5 % Final NRBC 0.0 0.0 - 0.2 /100 WBC Final NRBC Absolute 0.00 0.00 - 0.01 K/uL Final Platelet Count 366 150 - 450 K/uL Final Mean Platelet Volume 9.7 9.4 - 12.3 fL Final Neutrophils 67.9 40.0 - 70.0 % Final Immature Granulocytes 0.3 0.0 - 0.5 % Final Lymphocytes 26.0 22.0 - 44.0 % Final Monocytes 5.1 1.0 - 11.0 % Final Eosinophils 0.6 0.0 - 7.0 % Final Basophils 0.1 0.0 - 4.0 % Final Absolute Neutrophils 5.32 1.80 - 7.70 K/uL Final Absolute Immature Granulocytes 0.02 0.00 - 0.03 K/uL Final Absolute Lymphocytes 2.04 1.00 - 4.80 K/uL Final Absolute Monocytes 0.40 0.30 - 0.90 K/uL Final Absolute Eosinophils 0.05 0.00 - 0.50 K/uL Final Absolute Basophils 0.01 0.00 - 0.30 K/uL Final COMPREHENSIVE METABOLIC PANEL, NON-FASTING - Abnormal Sodium 139 135 - 145 mmol/L Final Potassium 4.2 3.5 - 5.0 mmol/L Final Chloride 102 101 - 111 mmol/L Final CO2 27 22 - 32 mmol/L Final Anion Gap 10 3 - 12 mmol/L Final Glucose, nonfasting 172 70 - 199 mg/dL Final BUN 12 8 - 20 mg/dL Final Creatinine 0.7 0.4 - 1.0 mg/dL Final Calcium 9.9 mg/dL Final Calcium, Adjusted 9.7 8.5 - 10.5 mg/dL Final Total Protein 8.1 6.0 - 8.5 g/dL Final Albumin 4.3 3.0 - 5.0 g/dL Final Albumin/Globulin Ratio 1.1 1.0 - 2.2 Ratio Final Bilirubin, Total 0.3 0.2 - 1.3 mg/dL Final Alkaline Phosphatase 96 38 - 126 IU/L Final AST (SGOT) 13 (*) 15 - 41 IU/L Final ALT (SGPT) 10 (*) 14 - 54 IU/L Final GFR, Estimate >60.0 >60 mL/min Final GFR, Interpretation see below Final URINALYSIS WITH MICROSCOPIC (CULTURE, IF INDICATED) - Abnormal Color, Urinalysis Colorless Final Turbidity, Urinalysis Clear Final Spec Grav, Urinalysis 1.005 1.001 - 1.035 Final pH, Urinalysis 6.5 5.0 - 8.0 Final Protein, Urinalysis Negative Neg Final Glucose, Urinalysis Normal Normal Final Ketones, Urinalysis Negative Neg Final Bilirubin, Urinalysis Negative Neg Final Occult Blood, Urinalysis Negative Neg Final Nitrites, Urinalysis Negative Neg Final Urobilinogen Normal Normal Final Leukocyte Esterase Negative Neg Final WBC, Urinalysis 0-5 0 - 5 /HPF Final RBC, Urinalysis 0-3 0 - 3 /HPF Final Sq. Epithelial Cells Occasional (*) None-Rare /LPF Final T4, FREE T4, Free 1.06 0.60 - 1.20 ng/dL Final TSH TSH 2.11 0.45 - 5.33 mIU/L Final TROPONIN-I, HIGH SENSITIVITY Troponin-I, High Sens 2.5 0.0 - 11.9 ng/L Final Pt given clonidine 0.1mg in ER and D/C home w/ RX for same Prior to DISCHARGE, vital signs are Temp: 36.6 ?C (97.9 ?F) Temp src: Oral Pulse: 81 BP: 121/79 SpO2: 100 % Oxygen Device: None (Room air). Repeat exam prior to discharge shows patient resting comfortably, symptoms improved, normal hemodynamics, feels ready to go home. 11/17 f/u Patient is currently having diarrhea, cough, fever, and body aches. Patient has not tested for Covid. Referal to Cardio. 11/18 f/u Pt reports SE from BP med. Pt reports taht she cant stand, cannot walk, she feels like she'll faint. Feels like her heart is racing at times, and her pulse is in the 90's. Advised patient to go to the ER. Checked with PA 11/18-11/21 ED to Hospital Admission HOSPITAL COURSE HPI: This is a 59-year-old female with past medical history of hyperlipidemia GERD recent diagnosis of hypertension who comes in secondary to generalized weakness and elevated blood pressure. As per the patient she received COVID booster 3 days ago and since then noticed that her blood pressure was running very high. She came to the ER and was prescribed clonidine which she started taking but still the blood pressure was running high and she felt very weak today and almost passed out so she decided to come in. The patient also noted that she started having a headache. Denies any chest pain no shortness of breath no cough no fever or chills. As per patient she has history of white coat syndrome, she has a log of her home blood pressure readings which are all within normal limits. In ER CTA was done. Hospital Course: Patient had multiple complaints while she was in the hospital. She had complains of dizziness, fluttering in her chest, diarrhea, and weakness in her bilateral lower extremity. Patient reported lot of the symptoms had started after she got her COVID booster. We offered her an MRI to look for any central lesion but patient adamantly refused and told us that she is not able to sit through closed MRI even with antianxiety medication. Her dizziness and chest fluttering did improve. She had gotten some meclizine and reported improvement. I have checked her orthostatic few times and she has been not orthostatic. In addition her EKG and CT had were negative as well for any acute disease. I also had physical therapy see her in consultation this morning. They recommended home PT for now which will be arranged. She had a CTA done in the ER for complains of chest fluttering and elevated blood pressure. My guess is they wanted to rule out aortic dissection. It was negative for dissection however patient was found to have 0.9 mm lung nodule on the right lower lobe, which Radiology recommended no follow-up if she has no other risk factors. In addition she was found to have a 2 x 2 x 2 cm cystic/masslike lesion in the pancreatic head. Patient denied any weight loss over the last 6 months. But I discussed this case with patient and Dr, oncologist who will arrange for outpatient biopsy as soon as this Wednesday. Patient voiced understanding. For her fluttering in her chest ED team, and the hospitalist team before me had spoken to on-call cardiologist who recommended outpatient follow-up. Patient was asked to follow with Dr for a ZIO patch Patient remained hemodynamically stable and the patient's biochemical profile was acceptable for discharge home to follow up with the patient's PCP and specialist in a few days to a week's time. Discharge plan and medications were reviewed with patient and/or family member who expressed agreement and understanding; all questions were answered to their satisfaction. PHYSICAL EXAM BP 141/83 | Pulse 82 | Temp 36.8 ?C (98.2 ?F) (Oral) | Resp 18 | Ht 154.9 cm (5' 1") | Wt 54.5 kg | SpO2 100% | BMI 22.70 kg/m? General: Pt in NAD HEENT: PERL, moist oral cavity Lungs: Not using accessory muscles of respiration, clear to auscultation bilaterally Heart: Regular rate and rhythm, no murmurs, gallops, or rubs Abdomen: Soft, non-tender, non-distended, normal active bowel sounds Extremities: No cyanosis or edema Neurological: No focal deficit PROCEDURES DURING THIS HOSPITALIZATION CONSULTS None IMAGING XR Chest 1 View Portable Result Date: 11/19/2022 Narrative: PROCEDURE: XR CHEST 1 VIEW PORTABLE HISTORY: chest discomfort COMPARISON: 11/15/2022 FINDINGS: Normal cardiomediastinal silhouette, lungs and pulmonary vasculature. No effusions or infiltrates are present. IMPRESSION: Normal chest. Finalized by MD at 11/19/2022 7:15 AM XR Chest 1 View Portable Result Date: 11/15/2022 Narrative: Examination:XR CHEST 1 VIEW PORTABLE Indication:Hypertension Comparison:None FINDINGS: No infiltrate or effusion. Cardiac size is within normal limits. IMPRESSION: No evidence of pneumonia or edema. Finalized by MD at 11/15/2022 3:28 PM CT Head or Brain without IV Contrast Result Date: 11/20/2022 Narrative: Patient: Time Out: 13:29 Exam(s): CT HEAD Without Contrast History: Reason for Exam: Dizziness, non-specific Additional notes: Blood pressure elevated without history of HTN Exam: CT HEAD Without Contrast Technique more: Axial noncontrast CT of the head with coronal, sagittal reformatted images. CTDI is 42.1 mGy and DLP is 733 mGy- cm. Technique more: Up-to-date CT equipment and radiation dose reduction techniques were employed. Comparison: 8/28/2021 Findings: Redemonstration of slightly prominent ventricles relative to the extra-axial CSF spaces. Negative for frank hydrocephalus. Gray-white matter differentiation is seen to be normal. Posterior fossa, cerebellar tonsils are unremarkable. Redemonstration of calcification of the pineal gland and slightly prominent sella turcica with partially empty sella on the right side. Mild calcification of the cavernous carotid. Opacified left and right sphenoid sinus. Impression: Impression: 1. No acute intracranial finding. 2. Redemonstration of slightly prominent right greater than left lateral ventricle especially frontal horn. Electronically signed by MD on 11-20-22 at 1329 CTA Chest Abdomen and Pelvis with and without IV Contrast Result Date: 11/18/2022 Narrative: Patient: Time Out: 20:42 Exam(s): CTA CHEST W/WO Contrast, CTA ABDOMEN + PELVIS W/WO Contrast IV Amt: IV: 125 EXAM: CT Chest Without and With Intravenous Contrast CLINICAL HISTORY: Reason for Exam: Thoracic aortic aneurysm (TAA) suspected Additional notes: Weakness - Generalized Pt with general weakness and feeling like passing out when standing since getting the COVID shot on Tuesday TECHNIQUE: Axial computed tomographic images of the chest without and with intravenous contrast. CTDI is 25.53 mGy and DLP is 668 mGy-cm. Up-to-date CT equipment and radiation dose reduction techniques were employed. CONTRAST: Patient received IV: 125 of IV contrast COMPARISON: CT 12-22-10 FINDINGS: Pulmonary arteries: Unremarkable. No pulmonary embolism or acute cardiopulmonary abnormality. Aorta: No acute findings. No thoracic aortic aneurysm. Other arteries: Punctate calcifications at the left anterior descending artery. Lungs: Right lower lobe pulmonary nodule measuring 0.9 mm in maximum transverse dimension. Pleural space: Unremarkable. No significant effusion. No pneumothorax. Heart: Unremarkable. No cardiomegaly. No significant pericardial effusion. No evidence of RV dysfunction. Bones/joints: Multilevel degenerative changes of the spine. No acute fracture. No dislocation. Soft tissues: Nonspecific calcifications within the breast bilaterally. Lymph nodes: Multiple enlarged lymph nodes at the left axilla. IMPRESSION: 1. No pulmonary embolism. 2. No evidence of thoracic aortic aneurysm or dissection. 3. Multiple enlarged lymph nodes at the left axilla. Correlate with lab values and recommend outpatient mammographic evaluation. 4. Right lower lobe pulmonary nodule measuring 0.9 mm in maximum transverse dimension. Fleischner Society Guidelines for low-risk patients, no follow-up is necessary. For high-risk patients (smoking history or other known risk factors) an optional chest CT at 12 months could be performed. _______________________________________________ EXAM: CT Abdomen and Pelvis With Intravenous Contrast CLINICAL HISTORY: Reason for Exam: Thoracic aortic aneurysm (TAA) suspected Additional notes: Weakness - Generalized Pt with general weakness and feeling like passing out when standing since getting the COVID shot on Tuesday TECHNIQUE: Axial computed tomographic images of the abdomen and pelvis with intravenous contrast. CTDI is 8.78 mGy and DLP is 349.98 mGy-cm. Up-to-date CT equipment and radiation dose reduction techniques were employed. CONTRAST: Patient received IV: 125 of IV contrast COMPARISON: No relevant prior studies available. FINDINGS: VASCULATURE: Aorta: No acute findings. No abdominal aortic aneurysm. No dissection. Celiac trunk and mesenteric arteries: No acute findings. No occlusion or significant stenosis. Renal arteries: No acute findings. No occlusion or significant stenosis. Iliac arteries: No acute findings. No occlusion or significant stenosis. Lung bases: Unremarkable. No mass. No consolidation. ABDOMEN: Liver: Unremarkable. No mass. Gallbladder and bile ducts: Status post cholecystectomy. No ductal dilation. Pancreas: Mixed cystic and solid partially enhancing lesion at the pancreatic head, measuring 2.1 x 2.1 x 2.0 cm suspicious for pancreatic neoplasm. No ductal dilation. Spleen: Unremarkable. No splenomegaly. Adrenals: Unremarkable. No mass. Kidneys and ureters: Unremarkable. No hydronephrosis. No solid mass. Stomach and bowel: Scattered diverticula in the colon. No diverticulitis. No obstruction. PELVIS: Appendix: No findings to suggest acute appendicitis. Bladder: Unremarkable. No mass. Reproductive: Unremarkable as visualized. ABDOMEN and PELVIS: Intraperitoneal space: Unremarkable. No significant fluid collection. No free air. Bones/joints: Multilevel degenerative changes of the spine. No acute fracture. No dislocation. Soft tissues: Unremarkable. Lymph nodes: Unremarkable. No enlarged lymph nodes. IMPRESSION: 1. No evidence of abdominal aortic aneurysm or dissection. 2. Mixed cystic and solid partially enhancing lesion at the pancreatic head, measuring 2.1 x 2.1 x 2.0 cm suspicious for pancreatic neoplasm. Recommend outpatient gastroenterology referral. Electronically signed by MD on 11-18-22 at 2042 USC Echo Complete Result Date: 11/20/2022 Narrative: Transthoracic Echocardiography Report (TTE) Demographics Patient Name Gender Female Patient Number Race Visit Number Age 59 year(s) Accession Number Date of Study 11/20/2022 Department Date of Birth REPORT: Sonographer Interpreting Physician MD Ordering Physician DO Copy To MD Procedure Type of Study TTE procedure:Echo-TTE. Priority: R Room: 3330Bed: P Procedure Date Date: 11/20/2022 Time: 10:25 AM Study Location: Portable Technical Quality: Limited visualization due to poor acoustical window. Indications:Chest pain. Additional Indications:Other (please specify). Patient Status: Routine Height: 60.98 inches Weight: 120.15 pounds BSA: 1.52 m^2 BMI: 22.71 kg/m^2 Rhythm: Within normal limits HR: 90 bpm BP: 128/56 mmHg Conclusions Summary This is a technically good study with the patient in sinus rhythm. Left ventricular wall thickness is at the upper limits of normal with preserved systolic and diastolic function. Visually estimated LVEF 60-65%. No segmental wall motion abnormalities. Morphologically normal valves with no regurgitation nor stenosis. No effusions. Essentially a normal study. No comparison study. Findings Left Ventricle The left ventricle is normal in size and function. The estimated ejection fraction is 60-65%. There are no regional wall motion abnormalities. The E/a ratio is consistent with normal diastolic function. E/e'<15, suggestive of normal left ventricular end diastolic pressure (LVEDP). Right Ventricle The right ventricle is normal in size and function. Left Atrium The left atrium is normal in size and appearance. The interatrial septum is intact with no evidence of atrial septal defect or patent foramen ovale by color flow doppler. Right Atrium The right atrium is normal in size and appearance. Aortic Valve The aortic valve is trileaflet. There is no aortic regurgitation. Mitral Valve The mitral valve is normal in structure and function. There is no mitral regurgitation. Pulmonic Valve The pulmonic valve is normal in structure and function. There is no pulmonic regurgitation. Tricuspid Valve The tricuspid valve is normal in structure and function. There is no tricuspid regurgitation. The right ventricular systolic pressure could not be estimated, due to insufficient tricuspid regurgitation signal. Great Vessels The aortic root dimension is within normal limits. The inferior vena cava appeared normal in size and decreased >50% with respiration (RAP 3mmHg). Pericardial Effusion There is no evidence of a significant pericardial effusion. Pleural Effusion There is no pleural effusion. M-Mode/2D Measurements & Calculations LV Diastolic Dimension: LV Systolic Dimension: LA Dimension: 2.3 cmAO 3.24 cm 2.23 cm Root Dimension: 2.7 cmLA LV FS:31.2 % LV Volume Diastolic: Area: 10.8 cm^2 LV PW Diastolic: 1.14 57.2 ml cm LV Volume Systolic: Septum Diastolic: 0.99 20.8 ml cm LV EDV/LV EDV Index: 57.2 ml/38 m^2LV ESV/LV LA/Aorta: 0.85 ESV Index: 20.8 ml/14 m^2 LA volume/Index: 23.6 ml LV Area Diastolic: 20.7 EF Calculated: 63.6 % /16m^2 cm^2 LV Area Systolic: 11.9 LV Length: 7.57 cm IVC Inspiration: 1 cm cm^2 Doppler Measurements & Calculations MV Peak E-Wave: 0.98 m/s AV Peak Velocity: 1.3 LVOT Peak Velocity: 0.86 MV Peak A-Wave: 0.89 m/s m/s m/s MV E/A Ratio: 1.1 AV Peak Gradient: 6.76 LVOT Peak Gradient: 3 MV Peak Gradient: 3.84 mmHg mmHg mmHg MV Mean Gradient: 1 mmHg MV Mean Velocity: 0.47 m/s PV Peak Velocity: 0.87 MV E' Septal Velocity: m/s 0.06 m/s PV Peak Gradient: 3.02 MV E' Lateral Velocity: mmHg 0.09 m/s Signature ---------------------------------------------------------------------------- Electronically signed by MD on 11/20/2022 11:34 AM ---------------------------------------------------------------------------- ECG 12 Lead - Standard Result Date: 11/19/2022 Narrative: Hospital Test Date: 2022-11-18 Pat Name: Department: EMERG Patient ID: Room: EMERG-- Gender: F Technician: DOB: Requested By: Order Number: Reading MD: Measurements Intervals Axis Rate: 83 P: 42 PR: 158 QRS: 20 QRSD: 90 T: 0 QT: 339 QTc: 399 Interpretive Statements SINUS RHYTHM SINCE EARLIER TRACING TODAY @ 14:56, NO SIGNIFICANT CHANGE 0000869324_20221118163730.pdf ECG 12 Lead - Standard Result Date: 11/19/2022 Narrative: Hospital Test Date: 2022-11-18 Pat Name: Department: EMERG Patient ID: Room: EMERG-- Gender: F Technician: DOB: Requested By: Order Number: Reading MD: Measurements Intervals Axis Rate: 81 P: 46 PR: 164 QRS: 34 QRSD: 86 T: 8 QT: 332 QTc: 386 Interpretive Statements SINUS RHYTHM SINCE 15 NOV 2022, NO SIGNIFICANT CHANGE 0000869324_20221118145659.pdf ECG 12 Lead - Standard Result Date: 11/15/2022 Narrative: Hospital Test Date: 2022-11-15 Pat Name: Department: 02 Patient ID: Room: EMERG-- Gender: F Technician: DOB: Requested By: Order Number: Reading MD: Measurements Intervals Axis Rate: 92 P: 27 PR: 157 QRS: 48 QRSD: 90 T: 39 QT: 348 QTc: 431 Interpretive Statements SINUS RHYTHM SINCE 28 AUG 2021, NO SIGNIFICANT CHANGE 0000869324_20221115142955.pdf RECENT LABS Recent Results (from the past 24 hour(s)) Basic Metabolic Panel, non-fasting Collection Time: 11/20/22 4:07 PM Result Value Ref Range Sodium 140 135 - 145 mmol/L Potassium 4.3 3.5 - 5.0 mmol/L Chloride 108 101 - 111 mmol/L CO2 27 22 - 32 mmol/L Anion Gap 5 3 - 12 mmol/L Glucose, nonfasting 136 70 - 199 mg/dL BUN 14 8 - 20 mg/dL Creatinine 0.8 0.4 - 1.0 mg/dL Calcium 8.9 mg/dL Calcium, Adjusted 9.1 8.5 - 10.5 mg/dL GFR, Estimate >60.0 >60 mL/min GFR, Interpretation see below ECG Rhythm Strip - Order Collection Time: 11/21/22 12:05 AM Result Value Ref Range ECG Interpretation NSR Results from last 7 days Lab Units 11/19/22 0443 11/18/22 1450 11/15/22 1447 WBC K/uL 5.99 5.04 7.84 HGB g/dL 10.3* 11.2* 10.9* HEMATOCRIT % 33.1* 36.6 36.2 Results from last 7 days Lab Units 11/20/22 1607 11/19/22 0443 11/18/22 1450 11/15/22 1447 SODIUM mmol/L 140 138 140 139 POTASSIUM mmol/L 4.3 3.2* 4.2 4.2 CHLORIDE mmol/L 108 103 105 102 CO2 mmol/L 27 26 27 27 BUN mg/dL 14 24* 10 12 CREATININE mg/dL 0.8 0.8 0.7 0.7 CALCIUM mg/dL 8.9 9.0 9.9 9.9 TOTAL PROTEIN g/dL -- 6.9 8.1 8.1 BILIRUBIN TOTAL mg/dL -- 0.3 0.3 0.3 ALK PHOS IU/L -- 81 89 96 ALT SGPT IU/L -- 12* 12* 10* AST SGOT IU/L -- 12* 16 13* 0 Lab Value Date/Time INR 1.0 (L) 08/28/2021 1912 Results from last 7 days Lab Units 11/19/22 1642 11/18/22 1450 MAGNESIUM mg/dL 2.0 2.0 FOLLOW UP PLAN PCP: MD F/U with dr, oncologist in 1 week and GI doctor for pancreatic mass biopsy . Follow up with Dr, heart doctor for a out patient zio patch Condition on Discharge: Stable Disposition: Home Discharge Activity: As tolerated Discharge Diet: Regular diet Pt later found to have neuroendocrine tumor of pancreas
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 3,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: GERD (gastroesophageal reflux disease) Hyperlipidemia Hypertension
- Andere Medikamente
- Medications: Meclizine 25mg omeprazole 20mg
- Allergien
- Allergies: Metoprolol (N/V), Levaquin (Rash), cipro (Rash), amlodipine (hives)
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Adjusted calcium
Alanine aminotransferase normal
Albumin globulin ratio
Angiogram abnormal
Angiogram pulmonary abnormal
Anion gap
Aspartate aminotransferase normal
Asthenia
Auscultation
Basophil count decreased
Basophil percentage decreased
Bilirubin urine
Blood albumin normal
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium decreased
Blood chloride increased
Blood creatinine normal
Symptomtext
Pt reported heart palpitations. Vitals: 220/112; 101,18 EMS Called @1320; Pt taken to ER IN ER: Pt was at covid vaccine clinic, 3 min after receiving vaccine, pt reports onset of continuous palpitations. Denies dizziness, SOB, N/V. C/o Right Rib pain for past few days. Hx of HTN. Patient is a 59 y.o. female who presents for evaluation of palpitations. Patient was at a vaccine clinic this afternoon, she had just received her COVID booster, when she began experience palpitations which has since improved and are now only intermittent. Staff took her blood pressure and found this to be elevated prompting EMS. Patient denies recent fevers/chills, illness/injury. At the time of interview no complaint for headache, change in vision, difficulty speaking, neck pain, chest pain, shortness of breath, back pain, abdominal pain, or new weakness/numbness/tingling to extremities. Pt describes left rib discomfort with palpation for the last few days (triage note not withstanding). 11/15 @14:37 36.6 ?C (97.9 ?F) 91 12 (!) 219/115 98 % Result Date: 11/15/2022 Narrative: Examination:XR CHEST 1 VIEW PORTABLE Indication:Hypertension Comparison:None FINDINGS: No infiltrate or effusion. Cardiac size is within normal limits. IMPRESSION: No evidence of pneumonia or edema. Finalized by MD at 11/15/2022 3:28 PM EKG: EKG interpretation EKG interpreted by myself -- Obtained at 1429 shows sinus, rate 92, no acute significant ST segment abnormalities, LABS: Labs Resulted Up to the Time of Admitted to the Floor CBC WITH DIFFERENTIAL - Abnormal Result Value Ref Range Status WBC 7.84 4.50 - 11.00 K/uL Final RBC 4.57 4.00 - 5.20 M/uL Final Hemoglobin 10.9 (*) 12.0 - 16.0 g/dL Final Hematocrit 36.2 36.0 - 46.0 % Final MCV 79.2 (*) 80.0 - 100.0 fL Final MCH 23.9 (*) 26.0 - 34.0 pg Final MCHC 30.1 (*) 31.0 - 37.0 g/dL Final RDW 14.3 11.5 - 14.5 % Final NRBC 0.0 0.0 - 0.2 /100 WBC Final NRBC Absolute 0.00 0.00 - 0.01 K/uL Final Platelet Count 366 150 - 450 K/uL Final Mean Platelet Volume 9.7 9.4 - 12.3 fL Final Neutrophils 67.9 40.0 - 70.0 % Final Immature Granulocytes 0.3 0.0 - 0.5 % Final Lymphocytes 26.0 22.0 - 44.0 % Final Monocytes 5.1 1.0 - 11.0 % Final Eosinophils 0.6 0.0 - 7.0 % Final Basophils 0.1 0.0 - 4.0 % Final Absolute Neutrophils 5.32 1.80 - 7.70 K/uL Final Absolute Immature Granulocytes 0.02 0.00 - 0.03 K/uL Final Absolute Lymphocytes 2.04 1.00 - 4.80 K/uL Final Absolute Monocytes 0.40 0.30 - 0.90 K/uL Final Absolute Eosinophils 0.05 0.00 - 0.50 K/uL Final Absolute Basophils 0.01 0.00 - 0.30 K/uL Final COMPREHENSIVE METABOLIC PANEL, NON-FASTING - Abnormal Sodium 139 135 - 145 mmol/L Final Potassium 4.2 3.5 - 5.0 mmol/L Final Chloride 102 101 - 111 mmol/L Final CO2 27 22 - 32 mmol/L Final Anion Gap 10 3 - 12 mmol/L Final Glucose, nonfasting 172 70 - 199 mg/dL Final BUN 12 8 - 20 mg/dL Final Creatinine 0.7 0.4 - 1.0 mg/dL Final Calcium 9.9 mg/dL Final Calcium, Adjusted 9.7 8.5 - 10.5 mg/dL Final Total Protein 8.1 6.0 - 8.5 g/dL Final Albumin 4.3 3.0 - 5.0 g/dL Final Albumin/Globulin Ratio 1.1 1.0 - 2.2 Ratio Final Bilirubin, Total 0.3 0.2 - 1.3 mg/dL Final Alkaline Phosphatase 96 38 - 126 IU/L Final AST (SGOT) 13 (*) 15 - 41 IU/L Final ALT (SGPT) 10 (*) 14 - 54 IU/L Final GFR, Estimate >60.0 >60 mL/min Final GFR, Interpretation see below Final URINALYSIS WITH MICROSCOPIC (CULTURE, IF INDICATED) - Abnormal Color, Urinalysis Colorless Final Turbidity, Urinalysis Clear Final Spec Grav, Urinalysis 1.005 1.001 - 1.035 Final pH, Urinalysis 6.5 5.0 - 8.0 Final Protein, Urinalysis Negative Neg Final Glucose, Urinalysis Normal Normal Final Ketones, Urinalysis Negative Neg Final Bilirubin, Urinalysis Negative Neg Final Occult Blood, Urinalysis Negative Neg Final Nitrites, Urinalysis Negative Neg Final Urobilinogen Normal Normal Final Leukocyte Esterase Negative Neg Final WBC, Urinalysis 0-5 0 - 5 /HPF Final RBC, Urinalysis 0-3 0 - 3 /HPF Final Sq. Epithelial Cells Occasional (*) None-Rare /LPF Final T4, FREE T4, Free 1.06 0.60 - 1.20 ng/dL Final TSH TSH 2.11 0.45 - 5.33 mIU/L Final TROPONIN-I, HIGH SENSITIVITY Troponin-I, High Sens 2.5 0.0 - 11.9 ng/L Final Pt given clonidine 0.1mg in ER and D/C home w/ RX for same Prior to DISCHARGE, vital signs are Temp: 36.6 ?C (97.9 ?F) Temp src: Oral Pulse: 81 BP: 121/79 SpO2: 100 % Oxygen Device: None (Room air). Repeat exam prior to discharge shows patient resting comfortably, symptoms improved, normal hemodynamics, feels ready to go home. 11/17 f/u Patient is currently having diarrhea, cough, fever, and body aches. Patient has not tested for Covid. Referal to Cardio. 11/18 f/u Pt reports SE from BP med. Pt reports taht she cant stand, cannot walk, she feels like she'll faint. Feels like her heart is racing at times, and her pulse is in the 90's. Advised patient to go to the ER. Checked with PA 11/18-11/21 ED to Hospital Admission HOSPITAL COURSE HPI: This is a 59-year-old female with past medical history of hyperlipidemia GERD recent diagnosis of hypertension who comes in secondary to generalized weakness and elevated blood pressure. As per the patient she received COVID booster 3 days ago and since then noticed that her blood pressure was running very high. She came to the ER and was prescribed clonidine which she started taking but still the blood pressure was running high and she felt very weak today and almost passed out so she decided to come in. The patient also noted that she started having a headache. Denies any chest pain no shortness of breath no cough no fever or chills. As per patient she has history of white coat syndrome, she has a log of her home blood pressure readings which are all within normal limits. In ER CTA was done. Hospital Course: Patient had multiple complaints while she was in the hospital. She had complains of dizziness, fluttering in her chest, diarrhea, and weakness in her bilateral lower extremity. Patient reported lot of the symptoms had started after she got her COVID booster. We offered her an MRI to look for any central lesion but patient adamantly refused and told us that she is not able to sit through closed MRI even with antianxiety medication. Her dizziness and chest fluttering did improve. She had gotten some meclizine and reported improvement. I have checked her orthostatic few times and she has been not orthostatic. In addition her EKG and CT had were negative as well for any acute disease. I also had physical therapy see her in consultation this morning. They recommended home PT for now which will be arranged. She had a CTA done in the ER for complains of chest fluttering and elevated blood pressure. My guess is they wanted to rule out aortic dissection. It was negative for dissection however patient was found to have 0.9 mm lung nodule on the right lower lobe, which Radiology recommended no follow-up if she has no other risk factors. In addition she was found to have a 2 x 2 x 2 cm cystic/masslike lesion in the pancreatic head. Patient denied any weight loss over the last 6 months. But I discussed this case with patient and Dr, oncologist who will arrange for outpatient biopsy as soon as this Wednesday. Patient voiced understanding. For her fluttering in her chest ED team, and the hospitalist team before me had spoken to on-call cardiologist who recommended outpatient follow-up. Patient was asked to follow with Dr for a ZIO patch Patient remained hemodynamically stable and the patient's biochemical profile was acceptable for discharge home to follow up with the patient's PCP and specialist in a few days to a week's time. Discharge plan and medications were reviewed with patient and/or family member who expressed agreement and understanding; all questions were answered to their satisfaction. PHYSICAL EXAM BP 141/83 | Pulse 82 | Temp 36.8 ?C (98.2 ?F) (Oral) | Resp 18 | Ht 154.9 cm (5' 1") | Wt 54.5 kg | SpO2 100% | BMI 22.70 kg/m? General: Pt in NAD HEENT: PERL, moist oral cavity Lungs: Not using accessory muscles of respiration, clear to auscultation bilaterally Heart: Regular rate and rhythm, no murmurs, gallops, or rubs Abdomen: Soft, non-tender, non-distended, normal active bowel sounds Extremities: No cyanosis or edema Neurological: No focal deficit PROCEDURES DURING THIS HOSPITALIZATION CONSULTS None IMAGING XR Chest 1 View Portable Result Date: 11/19/2022 Narrative: PROCEDURE: XR CHEST 1 VIEW PORTABLE HISTORY: chest discomfort COMPARISON: 11/15/2022 FINDINGS: Normal cardiomediastinal silhouette, lungs and pulmonary vasculature. No effusions or infiltrates are present. IMPRESSION: Normal chest. Finalized by MD at 11/19/2022 7:15 AM XR Chest 1 View Portable Result Date: 11/15/2022 Narrative: Examination:XR CHEST 1 VIEW PORTABLE Indication:Hypertension Comparison:None FINDINGS: No infiltrate or effusion. Cardiac size is within normal limits. IMPRESSION: No evidence of pneumonia or edema. Finalized by MD at 11/15/2022 3:28 PM CT Head or Brain without IV Contrast Result Date: 11/20/2022 Narrative: Patient: Time Out: 13:29 Exam(s): CT HEAD Without Contrast History: Reason for Exam: Dizziness, non-specific Additional notes: Blood pressure elevated without history of HTN Exam: CT HEAD Without Contrast Technique more: Axial noncontrast CT of the head with coronal, sagittal reformatted images. CTDI is 42.1 mGy and DLP is 733 mGy- cm. Technique more: Up-to-date CT equipment and radiation dose reduction techniques were employed. Comparison: 8/28/2021 Findings: Redemonstration of slightly prominent ventricles relative to the extra-axial CSF spaces. Negative for frank hydrocephalus. Gray-white matter differentiation is seen to be normal. Posterior fossa, cerebellar tonsils are unremarkable. Redemonstration of calcification of the pineal gland and slightly prominent sella turcica with partially empty sella on the right side. Mild calcification of the cavernous carotid. Opacified left and right sphenoid sinus. Impression: Impression: 1. No acute intracranial finding. 2. Redemonstration of slightly prominent right greater than left lateral ventricle especially frontal horn. Electronically signed by MD on 11-20-22 at 1329 CTA Chest Abdomen and Pelvis with and without IV Contrast Result Date: 11/18/2022 Narrative: Patient: Time Out: 20:42 Exam(s): CTA CHEST W/WO Contrast, CTA ABDOMEN + PELVIS W/WO Contrast IV Amt: IV: 125 EXAM: CT Chest Without and With Intravenous Contrast CLINICAL HISTORY: Reason for Exam: Thoracic aortic aneurysm (TAA) suspected Additional notes: Weakness - Generalized Pt with general weakness and feeling like passing out when standing since getting the COVID shot on Tuesday TECHNIQUE: Axial computed tomographic images of the chest without and with intravenous contrast. CTDI is 25.53 mGy and DLP is 668 mGy-cm. Up-to-date CT equipment and radiation dose reduction techniques were employed. CONTRAST: Patient received IV: 125 of IV contrast COMPARISON: CT 12-22-10 FINDINGS: Pulmonary arteries: Unremarkable. No pulmonary embolism or acute cardiopulmonary abnormality. Aorta: No acute findings. No thoracic aortic aneurysm. Other arteries: Punctate calcifications at the left anterior descending artery. Lungs: Right lower lobe pulmonary nodule measuring 0.9 mm in maximum transverse dimension. Pleural space: Unremarkable. No significant effusion. No pneumothorax. Heart: Unremarkable. No cardiomegaly. No significant pericardial effusion. No evidence of RV dysfunction. Bones/joints: Multilevel degenerative changes of the spine. No acute fracture. No dislocation. Soft tissues: Nonspecific calcifications within the breast bilaterally. Lymph nodes: Multiple enlarged lymph nodes at the left axilla. IMPRESSION: 1. No pulmonary embolism. 2. No evidence of thoracic aortic aneurysm or dissection. 3. Multiple enlarged lymph nodes at the left axilla. Correlate with lab values and recommend outpatient mammographic evaluation. 4. Right lower lobe pulmonary nodule measuring 0.9 mm in maximum transverse dimension. Fleischner Society Guidelines for low-risk patients, no follow-up is necessary. For high-risk patients (smoking history or other known risk factors) an optional chest CT at 12 months could be performed. _______________________________________________ EXAM: CT Abdomen and Pelvis With Intravenous Contrast CLINICAL HISTORY: Reason for Exam: Thoracic aortic aneurysm (TAA) suspected Additional notes: Weakness - Generalized Pt with general weakness and feeling like passing out when standing since getting the COVID shot on Tuesday TECHNIQUE: Axial computed tomographic images of the abdomen and pelvis with intravenous contrast. CTDI is 8.78 mGy and DLP is 349.98 mGy-cm. Up-to-date CT equipment and radiation dose reduction techniques were employed. CONTRAST: Patient received IV: 125 of IV contrast COMPARISON: No relevant prior studies available. FINDINGS: VASCULATURE: Aorta: No acute findings. No abdominal aortic aneurysm. No dissection. Celiac trunk and mesenteric arteries: No acute findings. No occlusion or significant stenosis. Renal arteries: No acute findings. No occlusion or significant stenosis. Iliac arteries: No acute findings. No occlusion or significant stenosis. Lung bases: Unremarkable. No mass. No consolidation. ABDOMEN: Liver: Unremarkable. No mass. Gallbladder and bile ducts: Status post cholecystectomy. No ductal dilation. Pancreas: Mixed cystic and solid partially enhancing lesion at the pancreatic head, measuring 2.1 x 2.1 x 2.0 cm suspicious for pancreatic neoplasm. No ductal dilation. Spleen: Unremarkable. No splenomegaly. Adrenals: Unremarkable. No mass. Kidneys and ureters: Unremarkable. No hydronephrosis. No solid mass. Stomach and bowel: Scattered diverticula in the colon. No diverticulitis. No obstruction. PELVIS: Appendix: No findings to suggest acute appendicitis. Bladder: Unremarkable. No mass. Reproductive: Unremarkable as visualized. ABDOMEN and PELVIS: Intraperitoneal space: Unremarkable. No significant fluid collection. No free air. Bones/joints: Multilevel degenerative changes of the spine. No acute fracture. No dislocation. Soft tissues: Unremarkable. Lymph nodes: Unremarkable. No enlarged lymph nodes. IMPRESSION: 1. No evidence of abdominal aortic aneurysm or dissection. 2. Mixed cystic and solid partially enhancing lesion at the pancreatic head, measuring 2.1 x 2.1 x 2.0 cm suspicious for pancreatic neoplasm. Recommend outpatient gastroenterology referral. Electronically signed by MD on 11-18-22 at 2042 USC Echo Complete Result Date: 11/20/2022 Narrative: Transthoracic Echocardiography Report (TTE) Demographics Patient Name Gender Female Patient Number Race Visit Number Age 59 year(s) Accession Number Date of Study 11/20/2022 Department Date of Birth REPORT: Sonographer Interpreting Physician MD Ordering Physician DO Copy To MD Procedure Type of Study TTE procedure:Echo-TTE. Priority: R Room: 3330Bed: P Procedure Date Date: 11/20/2022 Time: 10:25 AM Study Location: Portable Technical Quality: Limited visualization due to poor acoustical window. Indications:Chest pain. Additional Indications:Other (please specify). Patient Status: Routine Height: 60.98 inches Weight: 120.15 pounds BSA: 1.52 m^2 BMI: 22.71 kg/m^2 Rhythm: Within normal limits HR: 90 bpm BP: 128/56 mmHg Conclusions Summary This is a technically good study with the patient in sinus rhythm. Left ventricular wall thickness is at the upper limits of normal with preserved systolic and diastolic function. Visually estimated LVEF 60-65%. No segmental wall motion abnormalities. Morphologically normal valves with no regurgitation nor stenosis. No effusions. Essentially a normal study. No comparison study. Findings Left Ventricle The left ventricle is normal in size and function. The estimated ejection fraction is 60-65%. There are no regional wall motion abnormalities. The E/a ratio is consistent with normal diastolic function. E/e'<15, suggestive of normal left ventricular end diastolic pressure (LVEDP). Right Ventricle The right ventricle is normal in size and function. Left Atrium The left atrium is normal in size and appearance. The interatrial septum is intact with no evidence of atrial septal defect or patent foramen ovale by color flow doppler. Right Atrium The right atrium is normal in size and appearance. Aortic Valve The aortic valve is trileaflet. There is no aortic regurgitation. Mitral Valve The mitral valve is normal in structure and function. There is no mitral regurgitation. Pulmonic Valve The pulmonic valve is normal in structure and function. There is no pulmonic regurgitation. Tricuspid Valve The tricuspid valve is normal in structure and function. There is no tricuspid regurgitation. The right ventricular systolic pressure could not be estimated, due to insufficient tricuspid regurgitation signal. Great Vessels The aortic root dimension is within normal limits. The inferior vena cava appeared normal in size and decreased >50% with respiration (RAP 3mmHg). Pericardial Effusion There is no evidence of a significant pericardial effusion. Pleural Effusion There is no pleural effusion. M-Mode/2D Measurements & Calculations LV Diastolic Dimension: LV Systolic Dimension: LA Dimension: 2.3 cmAO 3.24 cm 2.23 cm Root Dimension: 2.7 cmLA LV FS:31.2 % LV Volume Diastolic: Area: 10.8 cm^2 LV PW Diastolic: 1.14 57.2 ml cm LV Volume Systolic: Septum Diastolic: 0.99 20.8 ml cm LV EDV/LV EDV Index: 57.2 ml/38 m^2LV ESV/LV LA/Aorta: 0.85 ESV Index: 20.8 ml/14 m^2 LA volume/Index: 23.6 ml LV Area Diastolic: 20.7 EF Calculated: 63.6 % /16m^2 cm^2 LV Area Systolic: 11.9 LV Length: 7.57 cm IVC Inspiration: 1 cm cm^2 Doppler Measurements & Calculations MV Peak E-Wave: 0.98 m/s AV Peak Velocity: 1.3 LVOT Peak Velocity: 0.86 MV Peak A-Wave: 0.89 m/s m/s m/s MV E/A Ratio: 1.1 AV Peak Gradient: 6.76 LVOT Peak Gradient: 3 MV Peak Gradient: 3.84 mmHg mmHg mmHg MV Mean Gradient: 1 mmHg MV Mean Velocity: 0.47 m/s PV Peak Velocity: 0.87 MV E' Septal Velocity: m/s 0.06 m/s PV Peak Gradient: 3.02 MV E' Lateral Velocity: mmHg 0.09 m/s Signature ---------------------------------------------------------------------------- Electronically signed by MD on 11/20/2022 11:34 AM ---------------------------------------------------------------------------- ECG 12 Lead - Standard Result Date: 11/19/2022 Narrative: Hospital Test Date: 2022-11-18 Pat Name: Department: EMERG Patient ID: Room: EMERG-- Gender: F Technician: DOB: Requested By: Order Number: Reading MD: Measurements Intervals Axis Rate: 83 P: 42 PR: 158 QRS: 20 QRSD: 90 T: 0 QT: 339 QTc: 399 Interpretive Statements SINUS RHYTHM SINCE EARLIER TRACING TODAY @ 14:56, NO SIGNIFICANT CHANGE 0000869324_20221118163730.pdf ECG 12 Lead - Standard Result Date: 11/19/2022 Narrative: Hospital Test Date: 2022-11-18 Pat Name: Department: EMERG Patient ID: Room: EMERG-- Gender: F Technician: DOB: Requested By: Order Number: Reading MD: Measurements Intervals Axis Rate: 81 P: 46 PR: 164 QRS: 34 QRSD: 86 T: 8 QT: 332 QTc: 386 Interpretive Statements SINUS RHYTHM SINCE 15 NOV 2022, NO SIGNIFICANT CHANGE 0000869324_20221118145659.pdf ECG 12 Lead - Standard Result Date: 11/15/2022 Narrative: Hospital Test Date: 2022-11-15 Pat Name: Department: 02 Patient ID: Room: EMERG-- Gender: F Technician: DOB: Requested By: Order Number: Reading MD: Measurements Intervals Axis Rate: 92 P: 27 PR: 157 QRS: 48 QRSD: 90 T: 39 QT: 348 QTc: 431 Interpretive Statements SINUS RHYTHM SINCE 28 AUG 2021, NO SIGNIFICANT CHANGE 0000869324_20221115142955.pdf RECENT LABS Recent Results (from the past 24 hour(s)) Basic Metabolic Panel, non-fasting Collection Time: 11/20/22 4:07 PM Result Value Ref Range Sodium 140 135 - 145 mmol/L Potassium 4.3 3.5 - 5.0 mmol/L Chloride 108 101 - 111 mmol/L CO2 27 22 - 32 mmol/L Anion Gap 5 3 - 12 mmol/L Glucose, nonfasting 136 70 - 199 mg/dL BUN 14 8 - 20 mg/dL Creatinine 0.8 0.4 - 1.0 mg/dL Calcium 8.9 mg/dL Calcium, Adjusted 9.1 8.5 - 10.5 mg/dL GFR, Estimate >60.0 >60 mL/min GFR, Interpretation see below ECG Rhythm Strip - Order Collection Time: 11/21/22 12:05 AM Result Value Ref Range ECG Interpretation NSR Results from last 7 days Lab Units 11/19/22 0443 11/18/22 1450 11/15/22 1447 WBC K/uL 5.99 5.04 7.84 HGB g/dL 10.3* 11.2* 10.9* HEMATOCRIT % 33.1* 36.6 36.2 Results from last 7 days Lab Units 11/20/22 1607 11/19/22 0443 11/18/22 1450 11/15/22 1447 SODIUM mmol/L 140 138 140 139 POTASSIUM mmol/L 4.3 3.2* 4.2 4.2 CHLORIDE mmol/L 108 103 105 102 CO2 mmol/L 27 26 27 27 BUN mg/dL 14 24* 10 12 CREATININE mg/dL 0.8 0.8 0.7 0.7 CALCIUM mg/dL 8.9 9.0 9.9 9.9 TOTAL PROTEIN g/dL -- 6.9 8.1 8.1 BILIRUBIN TOTAL mg/dL -- 0.3 0.3 0.3 ALK PHOS IU/L -- 81 89 96 ALT SGPT IU/L -- 12* 12* 10* AST SGOT IU/L -- 12* 16 13* 0 Lab Value Date/Time INR 1.0 (L) 08/28/2021 1912 Results from last 7 days Lab Units 11/19/22 1642 11/18/22 1450 MAGNESIUM mg/dL 2.0 2.0 FOLLOW UP PLAN PCP: MD F/U with dr, oncologist in 1 week and GI doctor for pancreatic mass biopsy . Follow up with Dr, heart doctor for a out patient zio patch Condition on Discharge: Stable Disposition: Home Discharge Activity: As tolerated Discharge Diet: Regular diet Pt later found to have neuroendocrine tumor of pancreas
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 3,0
- Labordaten
- see above
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: GERD (gastroesophageal reflux disease) Hyperlipidemia Hypertension
- Andere Medikamente
- Medications: Meclizine 25mg omeprazole 20mg
- Allergien
- Allergies: Metoprolol (N/V), Levaquin (Rash), cipro (Rash), amlodipine (hives)
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bronchitis
Condition aggravated
Cough
Fatigue
Headache
Oropharyngeal pain
Pruritus
Pyrexia
SARS-CoV-2 test negative
Symptomtext
I had a fever about five days after my COVID-19 shot. That then started me coughing and then I had a headache, sore throat, and was fatigued. I took several COVID-19 home tests and they were all negative. I was managing the symptoms with OTC medications but by mid-November I had my usual tell that I have bronchitis which is the middle of my back gets very itchy and I cannot get it stop. I was put on two rounds of antibiotics those helped and I did get better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- COVID-19 Home Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Bronchitis
- Andere Medikamente
- Amlodipine; Atorvastatin; Losartan; Loratadine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 09.01.2023
- Impfdatum
- 01.10.2022
- Beginn
- 14.12.2022
- Tage bis Beginn
- 74,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Basophil count increased
Blood creatinine decreased
Blood potassium decreased
Blood thyroid stimulating hormone normal
Blood urea decreased
Brain natriuretic peptide normal
Culture urine positive
Differential white blood cell count
Electrocardiogram ST segment abnormal
Eosinophil count increased
Full blood count
Hypertension
International normalised ratio normal
Metabolic function test
Monocyte count increased
Platelet count
Prothrombin time normal
Red blood cells urine
Symptomtext
My only symptom was the result of taking my blood pressure. I had no outside symptoms that would have let me know I was having high blood pressure. Since it was over 200/100, I went to the hospital. It got as high as 248/126. They gave me IV medication and kept me until they got it lowered. It took about five hours. They also told me to follow up with my doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- 12/14/2022 ECG, normal sinus rhythm, rightward axis, nonspecific ST abnormality; 12/14/2022 Urine culture, three or more organisms isolated, suggests contamination; 12/14/2022 RBC, UA, Urinary Tract Infection; 12/14/2022 TSH, normal; 12/14/2022 Protime INR, normal; 12/14/2022 Comprehensive Metabolic Panel: potassium low, BUN, high, creatinine low, BUN/Creatinine ratio, high, B-Type Natriuretic Peptide, normal; 12/14/2022 CBC W/PLAT Automatic Diff: Monocytes Relative, high, Eosinophils Relative, high, Basophils Relative, high
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis; Colitis
- Andere Medikamente
- LIPITOR; meloxicam; PRILOSEC; CLARITIN; IMODIUM; aspirin; lisinopril; probiotic; biotin
- Allergien
- Seasonal; dust; nickel
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 07.12.2022
- Beginn
- 08.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Discomfort
Dyspnoea
Headache
Pain
Symptomtext
Chest pain started in the morning after vaccination, it was a dull, achy pain with shortness of breath. Next came headaches the chest pain was uncomfortable for over 20 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Seasonal Allergies
- Andere Medikamente
- Vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 04.01.2023
- Impfdatum
- 05.10.2022
- Beginn
- 09.11.2022
- Tage bis Beginn
- 35,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood pressure increased
Blood test normal
Computerised tomogram normal
Decreased appetite
Mobility decreased
Nausea
Pain
Ultrasound scan normal
Urine analysis normal
Symptomtext
It began on Wednesday 11/9 with pain on my lower left side. It was only present when I was lying down in bed and tried to change positions. A week later on 11/16, I felt nauseous that evening and the following day. I went to the ER on 11/22. They did a lot of tests including CAT scan, blood work, and urine sample but were unable to pinpoint the cause of the pain. At that point the nausea was more concerning to me than the pain. For about 3 1/2 weeks I could only eat saltine crackers, nonfat Greek yogurt, bananas, mint, or ginger. Just looking at other food made me queasy. On Saturday 11/26 I had done about 6 hours of yardwork. Sunday 11/27 I did about 3 hours of yardwork and a lot of bending, but did not feel any pain during that time. Sunday night I experienced excruciating pain in my lower left side and very nauseous. I bought lidocaine patches but nothing helped. It became constant pain instead of just when I was laying down. I couldn't really bend over. I spent a lot of time laying down trying to use ice packs. I couldn't get comfortable sitting up in any position but I was comfortable standing up, or laying in certain positions. My PCP was unavailable but I spoke with a nurse at they started me on meloxicam. The nausea was extremely bad at this point. I took a few ROLAIDS on 12/4. I had a follow up with PCP on 12/6 and because the pain was so extreme she prescribed 50mg of tramadol for the pain, as needed, she also increased my blood pressure medication because my pressure had been still very high. On 12/7 I had a follow up ultrasound for a suspicious growth found through previous CAT scan, they said it was unrelated. On 12/12 I started physical therapy, and they prescribed a cane for my bad left knee and that has been helping with the pain some. On 12/25 was the least amount of pain I had been in since November. On 12/26 the pain returned but wasn't bad. As of 1/2/23 the pain has seemed to have disappeared, but my blood pressure remains high.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- CAT scan (11/22/22); blood work (11/22/22); Urine analysis (11/22/22); Ultrasound (12/7/22)
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Osteoarthritis; High Blood Pressure
- Andere Medikamente
- Lisinopril; ONE A DAY multivitamin
- Allergien
- Iodine; penicillin
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.01.2023
- Impfdatum
- 01.10.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 88,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Chest X-ray normal
Cough
Dyspnoea
Influenza virus test negative
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Salivary hypersecretion
Speech disorder
Streptococcus test negative
Symptomtext
I could not talk at all. It was excruciating pain in all of my throat. I needed a pain killer. I was breathing heavily like a purring cat or Darth Vader. I have runny nose, coughing, and spitting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 29DEC2022 Chest X-Ray negative; 29DEC2022 Influenza test negative; 29DEC2022 COVID-19 test positive; 29DEC2022 Strep throat test negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Pulmonary Hypertension
- Andere Medikamente
- Metoprolol; fenofibrate; levothyroxine; lisinopril; OPSUMIT
- Allergien
- Morphine; penicillin
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 31.12.2022
- Impfdatum
- 26.11.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 5,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea exertional
Symptomtext
shortness of breath; 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 77-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 26Nov2022 as dose 5 (booster), single (Lot number: GJ6739) at the age of 76 years, in left arm for covid-19 immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Vaccination history included: BNT162b2 (First Dose: , LOT: Unknown, there is no number listed on card, NDC, EXP: Unknown), administration date: 09Mar2021, when the patient was 75-year-old, for COVID-19 Immunization; BNT162b2 (Second Dose: , LOT: EP6955, NDC, EXP: Unknown), administration date: 01Apr2021, when the patient was 75-year-old, for COVID-19 Immunization; BNT162b2 (Third Dose: , LOT: thinks it is FC75327, NDC, EXP: Unknown), administration date: 10Nov2021, when the patient was 75-year-old, for COVID-19 Immunization; BNT162b2 (Fourth Dose: , LOT: FM9992, NDC, EXP: Unknown), administration date: 21Apr2022, when the patient was 76-year-old, for COVID-19 Immunization; Flu shot (Prior Vaccinations (within 4 weeks): Flu shot just before about 3 weeks before., Vaccine Name: Unknown, Manufacturer: Unknown , Lot Number/ Expiry Date: Unknown), for Immunization. The following information was reported: DYSPNOEA EXERTIONAL (non-serious) with onset Dec2022, outcome "not recovered", described as "shortness of breath". Additional information: As per agent and confirmed by caller, caller experienced shortness of breath after receiving his last Pfizer covid 19 booster; he is wanting to know if it will continue or will it go away. Upon request for details: caller received last vaccine shot on 26Nov2022. States about 1-1.5 weeks ago and 2 weeks after receiving the shot he noticed shortness of breath. Stated he only notices it when he walks. States he usually walks about 4 days a week and is able to walk about 6 times around a track and had no problems. Stated he is barely able to walk 6 times around the track and today was only able to walk 2 1/2 times around the track which is a big change for him. Stated he has a hcp appt next week. BNT162B2, BNT162B2 OMI BA.4-5 administered on 26Nov2022 with lot number: GJ6739 (Booster, fifth dose; left upper arm), Indication as got to take the booster, like everybody else. Shortness of breath was reported as worsened. Call regarding Covid-19 vaccine. Took 2 regular shots and the booster. Took last booster 26Nov2022, noticed about 2 weeks after took it, is now getting shortness of breath. When he got the shot, it started about 2 weeks after got it , was in Dec2022. Shortness of breath: Started around 2 weeks after 26Nov2022, when got the shot, was the second week and a half in Dec2022. Outcome: It started off a little lighter than it what it is now. Goes walking 4 days a week, for 30 minutes and has gotten a little worse. Usually, goes on a track 6 times before this. Now, gets to the first round and is ready to quit because of the shortness of breath. No Treatment. Clarified that caller had 3 boosters and 2 regular doses, for a total of five doses of the Covid-19 vaccine and, they were all Pfizer. Gets all that from the doctor and he has all of his medications on file. Test results: Got a nuclear stress test done just before getting the booster. No Family Medical History Relevant to Adverse Events (AEs). Just going to start walking for a while. If he can get through, can see if it will go away or not. If not, he would be in trouble. Other Conditions and Investigations: Unknown No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 30.12.2022
- Impfdatum
- 20.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Mobility decreased
Pyrexia
Symptomtext
Patient had fever 24 hours after administration but resolved within 48 hours after administration. Patient also had extreme fatigue and was unable to get out of bed which resolved within 48 to 72 hours after administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- none
- Allergien
- Pencillin
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 05.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Pruritus
Psoriasis
Skin exfoliation
Symptomtext
Itchy scaling, psoriasis flaring of which not noted until covid vaccinations. Lab tests done after previous
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- March 9, 2022 tests post-Moderna vaccination, dose 3. Lot #051F21A given on 11/08/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin, sulfa
- Vorherige Impfungen
- After 3rd Moderna covid vaccination on 11/02/2022, lot051F21A
- Staat
- WA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 23.12.2022
- Impfdatum
- 07.12.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 2,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Dyspnoea
Hypersomnia
Malaise
Poor quality sleep
Sleep disorder
Symptomtext
On December 9, 2022, two days after my dose 5, I began coughing heavily. I have not been feeling well and I am sleeping more. I would wake up coughing and I be awake for an hour because of my coughing. The cough has been affecting my breathing. I took some TYLENOL and ROBITUSSIN. On Saturday I went to the walk-in-clinic. I took benzonatate for a few days and that relieved my cough a bit. I am still not sleeping well due to waking up with my cough. I have had Asthma cough for so many years, but this cough is different.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Week of 11/24/2022 I had symptoms like the flu and started the bronchial cough but no chest pain.
- Vorgeschichte
- Asthma; Multiple Endocrine Neoplasia
- Andere Medikamente
- TYLENOL; vitamin C; aspirin; atorvastatin; calcium plus vitamin; CLARITIN; papaya tablets; albuterol inhaler
- Allergien
- Aspartame
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 23.12.2022
- Impfdatum
- 22.09.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 74,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Dyspnoea
Malaise
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I did not have an adverse event following my vaccination. On 12/05/2022, I began not feeling well with a cough, congestion and shortness of breath. I went to the emergency room on 12/07/2022 for six hours and tested positive for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 07DEC2022 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; Atrial Fibrillation
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 22.11.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arrhythmia
Arthralgia
Blood pressure increased
Blood test
Dyspnoea
Dysstasia
Insomnia
Pain
Productive cough
Supraventricular extrasystoles
Ventricular extrasystoles
Symptomtext
He got his vaccine, that night he just started to ache in general. The next day when he went to get up he could hardly stand up as his hips and knees hurt really badly. During the course of the day his breathing got very labored and coughing up phlegm. When he went to dialysis on Wednesday the nurses said he looked terrible and everything ached, and now 2 weeks later especially his hips hurt when he tries to get up from a sitting position due to the aching. As time has progressed as he got the vaccine his BP has been elevated, one day it was 215/105 and they have been giving him clonidine to knock it down. He did go to his doctor for a general look up and said that he was pretty good except for the post nasal problems, which continues and hear arrhythmias, but he has a history of heart disease. He had a heart attack for his 57th birthday and the next day he had a stroke. 2 months later he had a FU at the local Hospital and did not find any heart damage and had a FU 2 weeks later and was told he had another heart attack which damaged the lower part of his heart. He has noticed that after this booster he is having a lot of PAC's and PVC's, and especially when he lays down it gets a lot worse. He will probably have to go back to the cardiologist for that. He is having a lot of coughing, and not able to sleep due to that and the generalized aches and pains. He gets blood work every couple of weeks at the dialysis center, and had some today as well. He did have COVID back in 2020 and was hospitalized in a second hospital for 2 weeks and in a rehab facility for 17 weeks. He was supposed to be intubated and they did not do it, and so he survived.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- Bloodwork every 2 weeks at dialysis center.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Diabetes, high blood pressure, no kidney function and on dialysis.
- Andere Medikamente
- Micardis 80 mg, 81 mg aspirin.
- Allergien
- Zosyn (anaphylaxis).
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 20.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 11.12.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Injected limb mobility decreased
Injection site pain
Joint swelling
Mobility decreased
Pain
Symptomtext
Patient states he awake on 12-11-22 with a swollen left ankle, midsternum pain and generalized weakness, limited range of motion in bilateral arms. Reports that today his only symptom is pain to the right shoulder.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- seasonal allergies
- Andere Medikamente
- Benadryl daily - immunity vitamins OTC
- Allergien
- seasonal-hay fever
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 19.12.2022
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Vertigo
Symptomtext
Patient felt of having a vertigo a few minutes after the vaccination. Patient was asked to relax in the chair and was offered drinking water. After the vertigo symptoms went away, patient went home. She called back around 30 minutes later and mentioned having "chest pressure / tightness". Patient was asked to go the Emergency Room. Patient did not response to our follow-up phone calls.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- No
- Andere Medikamente
- Unknown
- Allergien
- No known allergy
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Condition aggravated
Hemiplegia
Migraine
Nausea
Pain
Sleep disorder
Vomiting
Symptomtext
I received the Pfizer Bivalent booster for COVID-19 on 12/5/2022 at around 11 AM. Later that night at around 8 PM, I began getting a migraine and nausea. I went to bed, and I was able to get to sleep. I woke up at about midnight vomiting. My pain was 9/10, and I continued vomiting. At about 4 AM on 12/6/2022, I woke my caregiver up and asked him to drive me to the hospital. When I got to the ER, they did not run any tests, because I have a long history of hemiplegic migraines with which they are familiar. Instead, they just gave me morphine and PHENERGAN to treat the pain and nausea, per instructions from my neurologist. I had to wait at the hospital for several hours before the medicines kicked in before they released me to go home in order to ensure that the medications were effective. When most of the pain had subsided, I was then released and then went home and went to bed. At the time of this writing, I am still recuperating from the hemiplegia. I have had hemiplegic migraines since 2003, and whenever I get them, I always experience paralysis of the right side of my body, from head to toe. After I received the first 3 doses of the Pfizer COVID-19 vaccine, I experienced hemiplegic migraines each time and had to go the ER on each occasion. On all of those occasions, I was treated with morphine and PHENERGAN, because those are the only things that work. Otherwise, I end up in the hospital for weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hemiplegic Migraines; Hypothyroidism; Ehlers-Danlos Syndrome; Acid Reflux Disease; High Cholesterol; Benign Extra Heartbeat.
- Andere Medikamente
- Multivitamin; probiotic; levothyroxine; omeprazole; famotidine; potassium RX; hydrochlorothiazide; estradiol; metoprolol; ezetimibe; atorvastatin; coQ10; BOTOX injections; nortriptyline.
- Allergien
- SEROQUEL; REGLAN; ZOFRAN; sulfa drugs; TEGRETOL; triptan drugs; ergotamine; erythromycin; TORADOL; COMPAZINE; melons; walnuts; all wasps.
- Vorherige Impfungen
- After all of my Pfizer COVID-19 shots and boosters, I have experienced hemiplegic migraines within 24 hours after receiving the
- Staat
- KS
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 07.12.2022
- Impfdatum
- 10.11.2022
- Beginn
- 25.11.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness postural
Hypotension
Symptomtext
I did not have an adverse reaction to the vaccine. On 11/25/22, I work up in the middle of the night and started to get up to go to the bathroom and got very lightheaded. I went on into the bathroom and got back to bed hoping to go back to sleep. I went to the emergency room for evaluation. My blood pressure was low and all other vitals where within normal range. The doctor and nurses in the emergency room said that I got up to fast. They told me I needed to slow down getting up in the morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Rheumatoid Arthritis; High Blood Pressure
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 06.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dizziness
Feeling hot
Headache
Hypoaesthesia oral
Malaise
Nausea
Oropharyngeal pain
Paraesthesia oral
Sensory disturbance
Symptomtext
About 20 minutes after a patient received the Pfizer bivalent booster, she started to feel sick. She felt hot, dizzy, severely nauseous, her tongue and lips felt numb and she felt weak. I checked her blood pressure and it was normal at 122/82. She reported no trouble breathing, but since her lips and tongue felt "weird" and numb, I administered 50mg of oral benadryl with her permission. We monitored her condition and her husband was called to come and pick her up. She was here for a total of one hour from the time the symptoms started and during that time some of them resolved, but she started to get a sore throat and severe headache. However, the nausea improved and she no longer felt hot. Patient continued to deny any difficulty breathing or sensation of swelling in her throat. She did not want 911 called. She felt if she went home and took ibuprofen and rested, she would be ok. She had some similar effects after her first two covid vaccine doses, but they did not start until approx 12 hours post vaccine administration and were not nearly this severe.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE REPORTED
- Vorgeschichte
- -
- Andere Medikamente
- BUPROPION, TRAZODONE, BUSPAR
- Allergien
- MORPHINE
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 01.12.2022
- Impfdatum
- 15.11.2022
- Beginn
- 27.11.2022
- Tage bis Beginn
- 12,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest X-ray
Discomfort
Dyspnoea
Hypertension
Painful respiration
Symptomtext
I started off being uncomfortable at night then I put a heating pad on it; when I woke up I was having discomfort breathing by noon I couldn't take any deep breath I could bend down or really move because it was cutting down my breathing; I couldn't take any deep breath because I had a sharp pain I went to emergency room my blood pressure was so high 204/97.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Chest x-ray; blood test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Lupus; Kidney transplant; Cardiovascular disease
- Andere Medikamente
- IMURAN; lisinopril; pravastatin; AREDS; UQORA; vitamin D3; probiotic 11; melatonin
- Allergien
- Antibiotics
- Vorherige Impfungen
- Fever
- Staat
- OR
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 01.12.2022
- Impfdatum
- 18.11.2022
- Beginn
- 24.11.2022
- Tage bis Beginn
- 6,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Condition aggravated
Influenza like illness
Pruritus
Rash
SARS-CoV-2 test negative
Symptomtext
Vaccinated 11/18/22; rash started 11/24/22 and has progressively spread from back to chest, axilla and now onto legs. Face is currently spared. Member seen by Dermatologist and given RX : TAC ointment ).05% applying daily. Itching is very intense: Benadryl gel seems to help. Member has Flu like symptoms , but is testing Covid negative. ( patient had a small rash mid low back, sacral area; that appeared after 4th vaccine in July 2022: was told a patch of psoriasis and given the Clobetasol Foam 0.05% to use bid). After this last vaccine: the back patch increased in size and then started to progress farther and farther out; now entire back , torso, chest, axilla and posterior legs are involved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Pulmonary embolisms since 2019 after Prostatectomy: taking Xarelto for life Depression: takes Citalopram
- Andere Medikamente
- Xarelto 10 mg per day, Atorvastatin 20 mg per day, Vitamin D3 50 mcg/day; Citalopram 40 mg: 1/2 pill per day; Metamucil daily; VSL # 3: probiotic weekly; Ketoconazole 2 % shampoo: once a week to scalp ; Clobetasol 0.05% topical foam appl
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.12.2022
- Impfdatum
- 20.11.2022
- Beginn
- 20.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chest pain
Decreased appetite
Fatigue
Headache
Pain
Pyrexia
Throat irritation
Vaccination site pain
Symptomtext
101 fever; arm site pain; body ache; scratchy throat; chest pain; headache; no appetite; tiredness; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 20Nov2022 at 17:45 as dose 3 (booster), single (Lot number: GJ6739) at the age of 61 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "obesity" (unspecified if ongoing); "rheumatoid arthritis fingers" (unspecified if ongoing), notes: rheumatold arthritis fingers; "sickle cell trait" (unspecified if ongoing); "Penicillin allergy" (unspecified if ongoing); "allergy to unspecified drug" (unspecified if ongoing), notes: unspecified drug used for nerve pain; "nerve pain" (unspecified if ongoing); "pre diabetic" (unspecified if ongoing); "food allergy" (unspecified if ongoing), notes: unspecified variety of food. The patient took concomitant medications. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, Lot number=EW0181,, Administration time=03:30 PM,, Vaccine location=Left arm), administration date: 16Jun2021, when the patient was 60-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE, Lot number=EW0181,, Administration time=12:30 PM,, Vaccine location=Left arm), administration date: 07Jul2021, when the patient was 60-year-old, for COVID-19 immunization. The following information was reported: PYREXIA (non-serious) with onset 20Nov2022 at 18:00, outcome "recovering", described as "101 fever"; VACCINATION SITE PAIN (non-serious) with onset 20Nov2022 at 18:00, outcome "recovering", described as "arm site pain"; PAIN (non-serious) with onset 20Nov2022 at 18:00, outcome "recovering", described as "body ache"; CHEST PAIN (non-serious) with onset 20Nov2022 at 18:00, outcome "recovering"; HEADACHE (non-serious) with onset 20Nov2022 at 18:00, outcome "recovering"; DECREASED APPETITE (non-serious) with onset 20Nov2022 at 18:00, outcome "recovering", described as "no appetite"; THROAT IRRITATION (non-serious) with onset 20Nov2022 at 18:00, outcome "recovering", described as "scratchy throat"; FATIGUE (non-serious) with onset 20Nov2022 at 18:00, outcome "recovering", described as "tiredness". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of pyrexia, vaccination site pain, pain, throat irritation, chest pain, headache, decreased appetite, fatigue. Additional information: other medications in two weeks included blood pressure medicines, multi vitamins and minerals.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Name: fever; Result Unstructured Data: Test Result:101 Fahrenheit
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Drug allergy (unspecified drug used for nerve pain); Food allergy (unspecified variety of food); Nerve pain; Obesity; Penicillin allergy; Pre-diabetic; Rheumatoid arthritis (rheumatold arthritis fingers); Sickle cell trait
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 25.11.2022
- Impfdatum
- 02.11.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angina pectoris
Anxiety
Back pain
Blood pressure increased
Chest X-ray normal
Cold sweat
Condition aggravated
Dyspnoea
Extrasystoles
Fatigue
Feeling abnormal
Hot flush
Hyperhidrosis
Hypertension
Influenza like illness
Malaise
Menopause
Pain
Symptomtext
She got her vaccines, had the sore arm as expected. She was told that she could not take any Ibuprofen which is the only pain medicine that works for her. By 10:30 that night it came on very suddenly and was full into feeling bad, flu-like symptoms. She took Alka-Seltzer night-time severe cold and flu, drank that and she was miserable with high fever but did not register it, was drenched with sweat and also suffers from hot flashes as she is going through menopause. She then started having heart palpitations, and felt that it was from the Alka-Seltzer, but that feeling has never left her since stopping the medicine. She gets them around her heart, feels tense and stressed. She has a panic disorder also which she's having the reactions to the vaccine and the palpitations, which she cannot deal with it. She has recently moved and as an APT in January and called to see what to do and was informed that she could treat her for that. When she lies down she cannot breathe and also continues with the heart palpitations. She went to the ER on 11/19/22 after her doctor said she could treat her, a friend felt that she may be having a heart attack. She had an out patient sonogram who was informed by the tech that her heart was skipping a beat. On 11/23/22 she called the doctors office to check and see what was going on as she was feeling like she was going to have a heart attack, and told her that everything was normal. She has been feeling all the symptoms since she's had the vaccines. The arm itself are fine, and the symptoms are "hell", she has the intermittent skipped beats, palpitations, and not feeling well. The symptoms and the panic disorder are bouncing off each other and is not on any APT's to treat it. she has an APT with the cardiologist on 12/2/22, and is not taking that there is nothing wrong with her as the symptoms are horrendous. She had 2 very high BP readings in the ER, and due to the recent move she cannot get into a PCP sooner. When she has the random reaction she gets pain, hollers with the pain, starts on the left, and then moves to the right and spreads around which triggers her anxiety. She has a lot of back pain and feels like her lungs are hurting and feels like she has been kicked in the back on the back side of her heart, underneath the shoulder blade. She also has a dull pain from her heart which like her heart is not relaxed. She did have a chest x-ray and it was clear. She feels like she is about to die, she is tired and feels real bad. The cold sweats are scary too which is different from her menopause symptoms. She does have elevated blood pressure, but is not on any BP medicine at this time and needs some relief from her symptoms. She went to ER. Her DC DX as chest pain, unspecific type and anxiety.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- In the ER.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Anxiety and depression.
- Andere Medikamente
- None.
- Allergien
- Latex, Depo-Provera shot gave her a reaction.
- Vorherige Impfungen
- Had a Depo-Provera vaccine which made her go crazy, and had to be hospitalized for the symptoms.
- Staat
- OH
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 25.11.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Confusional state
Dizziness
Dyspnoea
Flushing
Hyperhidrosis
Hypotension
Nausea
Tremor
Visual impairment
Symptomtext
Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Chills-Medium, Systemic: Confusion-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Systemic: Nausea-Medium, Systemic: Shakiness-Mild, Systemic: Visual Changes/Disturbances-Mild, Additional Details: we called 911 for pt after he had all these symptoms.he laid down on the floor and we elevated his legs.it took hom up to 25 mon to feel bettwe and go home.he did not go urgent care after that .he went home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 22.11.2022
- Impfdatum
- 08.10.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 24,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Faecal calprotectin increased
Gastrointestinal inflammation
Inflammatory bowel disease
Laboratory test
Magnetic resonance imaging
Scan with contrast
Symptomtext
IBD worsening - Increased intestinal inflammation (very high calprotectin), still doing tests. MRI and colonoscopy on the way. From my first report, my first IBD symptoms started in December after first Covid booster in November 2021. And I also had my first ever flu shot that year in September. In summer 2022 I also had issues with liver (elevated liver enzymes) after a booster shot in July 2022. Got liver biopsy and diagnosed with Primary Sclerosing Cholangitis. Currently taking Ursodiol and there is no treatment for PSC. Waiting to change medication for IBD because Entyvio doesn?t seem to work. Potentially, my iron supplement might be exacerbating intestinal inflammation. So I?ve stopped taking it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- For this flare I?ve had lab tests in late October. MRI enterography with contrast on November 17, will have colonoscopy on December 30. Liver biopsy in September. And liver ultrasound and MRI in August
- Aktuelle Erkrankungen
- IBD (ulcerative colitis), Primary Sclerosing Cholangitis.
- Vorgeschichte
- Asthma, allergies, Mitral valve prolapse
- Andere Medikamente
- Ursodiol, Entyvio, loratadine, iron, vitamin D, omega 3, folic acid, calcium
- Allergien
- Aspirin and NSAIDs
- Vorherige Impfungen
- IBD symptoms within a month after first Covid booster in 2021. I have a separate report for this.
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 21.11.2022
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Hypertensive crisis
Malaise
Tachycardia
Symptomtext
received bivalent booster. Pt reported to observation staff that she was not feeling well following Pfizer Bivalent vaccine. RN took vital signs. BP was 220/117 and tachycardic. Pt's vitals taken every five minutes. Pt remained in hypertensive crisis. 911 called. No previous hx of HTN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 10.11.2022
- Impfdatum
- 10.11.2022
- Beginn
- 10.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Cold sweat
Dizziness
Dyspnoea
Headache
Nausea
Pain
Pain in extremity
Symptomtext
On November 10, 2023 at approximately 1:50pm after receiving her COVID-19 Vaccine, Guest complained of Shortness of Breath, pain radiating from her left side of head down to her left arm, tightness in her left chest, dizziness and nausea. Vital taken: BP 148/98, HR 92, Cool & Clamy to touch. EMS was notified and responded. Patient was checked by paramedics and refused transport to the nearest hospital for treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypertension
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 01.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 6,0
- Dosis
- N/A
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Enlarged uvula
Hypotension
Rash
Swelling face
Urticaria
Symptomtext
Rash 57 hours after, rash with hives 59 hours after, swelling of face and diffuse rash and hives, hypotension and uvula swelling 70 hours after
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Common cold 2 weeks prior
- Vorgeschichte
- -
- Andere Medikamente
- Wellbutrin Trazadone Progesterone Estradiol
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 07.11.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Choking
Cough
Dyspnoea
Pain
Secretion discharge
Sleep disorder
Symptomtext
Severe increase in breathing difficulty, I had to resort to O2 use constantly.Without the O2 my Pulseox was reading an average of 87 with no energy spent and would drop into the low 80s from just walking. Normal range in the 90s. I also was unable to sleep more than two hours at night. I could not lay down without a buildup of mucous which would choke me, I had to use my rescue inhaler and I was coughing excessively . Also had body aches. This lasted just over two weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COPD, Bronchiestasis, Asthma, Emphysema, Kidney Failure
- Andere Medikamente
- Atorvastatin 40mg, Trintellex 20mg, Furosemide 5 mg, Olmesartan Medoximil 40mg, Amlodipine besylate 5 mg, omeprazole DR 20 mg, Pramipexole 1 mg, Azithromycin 250 mg, Levocetrizine 5 mg, Ventalin, Trilogy, Dupixent, Azelastine nasa
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 20.10.2022
- Beginn
- 22.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Dry throat
Dyspnoea
Fatigue
Fungal infection
Rash
Rash erythematous
Symptomtext
About two days after receiving my fifth dose of the Pfizer Bivalent vaccine, I started to feel fatigued. I was experiencing shortness of breath and just really tired. It was hard for me to catch my breath when I went outside of my house. I knew something was going wrong because my throat was staying dry. When I went to my doctor, she told me that I have a fungus in the back of my throat. She gave me the mouthwash to help with that. I also noticed that I had a red rash show up on my leg, but as of yesterday it was no longer present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Esophageal exam; blood work;
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- A-Fib; Hypertension; Anemic; Cancer survivor; Hernia operations; hysterectomy; DVT; Blood clots in lungs; Lupus; back surgery; Total knee replacement; anxiety
- Andere Medikamente
- Warfarin; potassium; temazepam; OTC allergy relief; maleate; carvilol; stool softener; pantoprazole; topiramate; linzess; bariatric advantage ultra multivitamin without iron; Tizanidine HCL; pregablin; levotetirizine; Vitamin D3; Atorvasta
- Allergien
- A chemo drug; dust mites
- Vorherige Impfungen
- Flu Vaccine, September 2022, I started to have minor breathing problems.
- Staat
- CO
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Crying
Insomnia
Malaise
Mobility decreased
Oropharyngeal pain
Pain in extremity
Product administered to patient of inappropriate age
Pyrexia
Symptomtext
10 YEAR OLD PATIENT WAS INADVERTANTLY GIVEN ADULT PFIZER BIVALENT 12+ WHEN CONTACTED , THE FATHER SAID HIS DAUGHTER WAS NOT FEELING WELL AT ALL AND DIDN'T GO TO SCHOOL THE FOLLOWING DAY. HER SYMPTOMS INCLUDED AN EXTREMELY SORE ARM THAT SHE SAID FELT LIKE SHE COULD NOT MOVE IT, A SORE THROAT, LOW-GRADE FEVER, SHE WOKE UP CRYING AND AND HAD TROUBLE SLEEPING DURING THE NIGHT DUE TO PAIN. HE STATED THAT SHE TOOK IBUPROFEN FOR PAIN, DOSE UNKNOWN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NOT AT TIME OF VACCINATION, NOT KNOW PRIOR
- Vorgeschichte
- NOT KNOWN
- Andere Medikamente
- NOT KNOWN
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 26.10.2022
- Impfdatum
- 26.09.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Computerised tomogram head
Condition aggravated
Electroencephalogram
Magnetic resonance imaging head
Temporal lobe epilepsy
Symptomtext
Recurrence of the somatosensorial epilepsy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- EEG and brain CT on Oct 10, 2022 and MRI brain Scan on Oct 22
- Aktuelle Erkrankungen
- had somatosensorial epilepsy for a venous event in the right hemispheric central sulcus; treated with eslicarbazepine 2017-2020 then completely recovered
- Vorgeschichte
- mitral valve cardiac anuloplasty in 1998; cardioversion for atrial fibrillation in October 2020
- Andere Medikamente
- Flu Vaccine Concomitant
- Allergien
- cat fur
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 24.10.2022
- Impfdatum
- 16.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Paraesthesia
Pyrexia
Symptomtext
On 10/17/22, around 4:00AM I had fever, chills, and shivers. On 10/18/2022 around 8AM to 10AM I became aware of having tingling sensation in my extremities. The tingling sensation is primarily in the bottom left sole of my foot. After that day I started exercising the sensation spread from the left foot to both of my pinkies, ring fingers and both of my hands. For the hand after an hour the tingling did go away. The foot tingling is off and on. It seems to come and is pronounced when I put pressure on the foot. When I exercise it sometimes spreads to my right foot, but the tingling is predominantly on my left foot. I contacted my doctor by email, and she recommended to use ibuprofen and that did help my fever. I did that for 3 to 5 days. On 10/24/2022 I had a checkup with my doctor. The doctor ruled out prediabetes. She did a stroke test. She referred me to a neurologist. I have recovered from the fever and chills. I am still experiencing the tingling in my left foot. Sometimes when I exercise, the tingling does spread to other extremities.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Not yet.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Fish oil; vitamin D3
- Allergien
- None
- Vorherige Impfungen
- Tetanus, 2008, I came close to fainting.
- Staat
- OH
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Condition aggravated
Dizziness
Throat tightness
Symptomtext
Patient reported that she has anxiety and some medical procedures make her feel lightheaded. Administered flu (FluBlok) and COVID-19 (Pfizer bivalent) vaccinations to patient. Patient was ok after vaccinations and moved to waiting area. after a couple minutes, patient stated she was feeling lightheaded and moved to floor in counseling/vaccination room. provided patient cool compress and bottled water. she also reported her throat feeling tightness but acknowledged it was anxiety. patient did not show other signs of anaphylaxis and was able to breath, talk, and drink water without difficulty. after ~15 minutes patient moved to chair in counseling room. after ~5 minutes patient moved to chair in waiting room. after ~5 minutes, patient left pharmacy area to shop in store.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- anxiety
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Eye irritation
Feeling abnormal
Lymph node pain
Mobility decreased
Muscular weakness
Oropharyngeal pain
Rhinorrhoea
Symptomtext
She got her vaccine, had no reaction. Thursday morning her arm was still fine. About 8:00 PM she was laying in bed watching TV, her nose started to run, her throat was hurting and her eyes were burning. She was having trouble breathing, took her inhaler, her legs felt like jello, lymph node under her right arm was painful and was not able to get out of bed. She called the HCF and they told her that it takes 48 hours for the antibodies to start and to call her PCP. She called him and was started on Augmentin on Friday. Thursday night she started to take Mucinex, then the antibiotics and felt like she was going to die. She is starting to feel better today. She felt so bad that she was going to call 9-1-1. Her doctor told her that he felt that it was the lymph node under the arm too. She is scheduled for blood work on Thursday and is going to look at it then. With her J&J vaccines she had some soreness in her arm, but nothing severe and was gone in a day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Fibromyalgia and high blood pressure, stroke in 2016.
- Andere Medikamente
- Vitamin B-complex, magnesium, baby aspirin, Vitamin D3, Clopidogrel 75 mg, Valsartan 80 mg, Nifedipine 30 mg, Celebrex 200 mg.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 03.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 18,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Arrhythmia
Blood test
Chest pain
Electrocardiogram
Injection site pain
Pain
Symptomtext
PATIENT STARTED HAVING CHEST PAIN AT 1600 ON 10.21.2022 THAT RADIATED DOWN HER LEFT ARM. SHE TOOK A NITROGLYERIN AND CAME TO THE ER. PATIENT WAS ADMITTED DUE TO DYSRHYTHMIAS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- ECG, BLOOD LABS ON 10.21.2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- TIA, CORONARY ARTERY DISEASE, CONGESTIVE HEART FAILURE, HYPERLIPIDEMIA, HYPERTENSION, AORTA-ILIAC-FEMORAL BYPASS, MITRAL VALVE STENOSIS, PERIPHERAL ARTERIAL DISEASE
- Andere Medikamente
- ASPIRIN, CARVEDILOL, VITAMIN D3, PLAVIX, LOSARTAN, MECLIZINE, NITROGLYCERIN, FISH OIL, APRODINE, ROSUVASTATIN, SPIRONOLACTONE
- Allergien
- PENICILLIN, CLINDAMYCIN
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 20.10.2022
- Impfdatum
- 16.10.2022
- Beginn
- 18.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Angiogram pulmonary normal
Anxiety
Chest X-ray normal
Chest discomfort
Chest pain
Creatinine renal clearance normal
Differential white blood cell count normal
Dyspnoea
Electrocardiogram normal
Fatigue
Fibrin D dimer increased
Full blood count normal
Injection site pain
Laboratory test normal
Metabolic function test normal
Prohormone brain natriuretic peptide
Troponin I
Symptomtext
Started getting moderate chest pressure and minor shortness of breath at 12pm October 18th. These symptoms were constant through out the remainder of the day. The symptoms got worse and included sharp, aching chest pain if I was active (even lightly active walking less than a mile at a normal pace). By 11pm, I became a bit worried so I went to the ER to be evaluated incase it was related to the vaccine. Aside from these symptoms, I only had mild fatigue and arm pain at both injection sites (flu and COVID).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- All tests and labs performed in early AM of 10/19/22 Chest Xray - normal CT Angio Chest Pulmonary Emoli - normal ECG - normal Vitals - normal D Dimer - slightly elevated Hs Trop 1 through 3 - negative/normal Pro BNP - normal Lipase - normal Est CrCI - Normal Auto Diff - normal CBC/Diff - normal CMP - normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Acid reflux (periodic)
- Andere Medikamente
- 50mg Zoloft Azelastine spray Montelukast Sod Alli Multivitamin
- Allergien
- Dust mites Venlafaxine Some general anesthesia (I have malignant hyperthermia) Liquid fabric softner
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 17.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 9,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dyspnoea
Fatigue
Headache
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I tested positive for COVID-19 on 10/10/22. On 10/8/22, I woke up with a sore throat and tested negative with an at home test. On 10/9/22, I had coughing, headache, congestion, fatigue and this continued until 10/10/22. I started having visions of going on a ventilator and I became concerned about my breathing. I went to the clinic and was prescribed Albuterol Sulfate, and 20mg Prednisone twice a day for five days. My primary doctor started me on Paxlovid for five days. I have two more doses to finish that up. I have steadily started to feel better, but I am still testing positive at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test - 10/10/22 - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; GERD, High Cholesterol; Neuropathy; Enlarged Prostate
- Andere Medikamente
- Omeprazole; Hydrochlorothiazide; Finasteride; Meloxicam; Oxybutynin Chloride; Gabapentin; Tamsulosin; Atorvastatin; CBD; Multivitamin; Ultimate Omega; Alpha Lipoic
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 15.10.2022
- Impfdatum
- 15.10.2022
- Beginn
- 15.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Paraesthesia
Peripheral coldness
Visual impairment
Symptomtext
Pt describes narrowing/spotty vision and prickling sensation in the fingers/ feeling cold in the extremities that improved after about 30 minutes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- dextroamphentamine
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 08.10.2022
- Impfdatum
- 08.10.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Chest discomfort
Electrocardiogram
Feeling jittery
Flushing
Laboratory test
Palpitations
Paraesthesia oral
Symptomtext
Patient received bivalent -pfizer Lot: GJ6739 at 12:35pm Patient went to car and started driving and felt her heart "racing" and she felt jittery. She stated that her tongue was tingling as well and turned her car around and came back to the COVID center. The front desk notified nurses and she was put on a cart Patient denies allergies and no other illness at time of vaccination. Denies and chronic or long standing conditions. Patient states she never had a reaction to any vaccine. Summary: 12:55 143/82 Pulse 108 res 20 Pulse ox 100%- patient states she feels jittery, tongue tingling, no airway issues, heart racing: 1 pm 125/77 HR 104 Resp 20 Pulse Ox 100% "feeling just a little better, face feels flushed, heart not racing as much but chest still feels tight, 1:05: 138/92 HR 188 Resp 22 Pulse ox 100% 1:10 Staff walked over and BP 140/90 HER 156- Patient very anxious. 1:11 Activated 911. 1:13 138/92 Pulse 110 Pulse ox 100% 1:16 143/86 HR 114 Pulse ox 100% 1:17 EMS arrived assessed patient. Patient remained anxious and wished to go to the ER. Husband- and son were with patient and went to the ER once patient left in ambulance. Nurse: Rn Scribe : RN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Patient went to the ER, Labs, EKG, drawns
- Aktuelle Erkrankungen
- denies
- Vorgeschichte
- denies
- Andere Medikamente
- none asked
- Allergien
- denies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 26.09.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 8,0
- Dosis
- 5
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Blood test normal
Cardiac flutter
Electrocardiogram normal
Impaired driving ability
Palpitations
Symptomtext
It felt like my heart was fluttering/racing and I was so lightheaded that I had trouble driving my car. I was on my way out of town to meet some friends but instead drove to the emergency room. They performed an EKG and some blood tests. All were normal. As I sat there waiting for the test results, I started to feel better. I never passed out and they released me. I drove home without incident and the following day I drove 3 hours to meet my friends. I have been experiencing the fluttering sensation every day since, but not as intense and as debilitating as the first day (which was Tuesday, Oct. 4). I am following up with my cardiologist but have not yet been able to schedule an appointment with him.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- EKG and blood tests - October 4, 2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin C; Vitamin D3
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 30.09.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Heart rate increased
Paraesthesia
Symptomtext
PATIENT REPORTED HAVING DIZZINESS INITIALLY THEN FASTER HEART BEAT & BODY TINGLING; PARAMEDIC TOOK PATIENT TO HOSPITAL FOR MEDICAL CARE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 27.12.2023
- Impfdatum
- 16.11.2022
- Beginn
- 31.10.2023
- Tage bis Beginn
- 349,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Blood creatinine increased
COVID-19
Chest X-ray abnormal
Chronic fatigue syndrome
Chronic kidney disease
Gait disturbance
Interstitial lung disease
Malaise
SARS-CoV-2 test positive
Symptomtext
Patient is a 81 y.o. male patient of CNP with history of COPD, chronic hypoxemic respiratory failure on 4 to 5 L of oxygen at home, atrial fibrillation, congestive heart failure, aortic valve disease s/p TAVR, hypertension, hepatitis B and pulmonary hypertension presented to Hospital with weakness on 10/31/2023. The following describes as Hospital course by problem: Covid-19 Virus Infection Date of onset of symptoms: 10/25/2023 Symptoms present on admission: Weakness Date of covid positive test: 10/31/23 Vaccination status: vaccinated Imaging: CXR with chronic interstitial changes Oxygen requirements on admission: 5 Lpm (baseline 5 Lpm) Current oxygen requirements: 5 Lpm Medical therapy: Started on IV remdesivir first dose 11/03 and IV Decadron Consultants following: ID Infectious disease following and completed course of remdesivir while inpatient and treated with steroids. At baseline respiratory status at time of discharge. Chronic hypoxemic respiratory failure COPD Severe pulmonary hypertension, Baseline oxygen 4 to 5 Lpm by NC Continue Spiriva, Dulera Albuterol PRN Generalized weakness: Chronic fatigue syndrome Ambulatory dysfunction Evaluated by therapy Declined home health services Chronic kidney disease Creatinine baseline ranging around 1.3 Monitor BMP daily And euvolemic continue home med torsemide Cr down to 1.06 Chronic diastolic heart failure: Remains euvolemic Continue torsemide Continue home medications including metoprolol Severe pulmonary hypertension: Continue riociguat 3 times daily HTN: Norvasc, Toprol Atrial fibrillation S/p Amulet device implantation; scheduled for CTA and possible discontinuation of anticoagulation in future Continue home meds Tikosyn, Toprol and Coumadin Follow-up with INR clinic on Monday Chronic Anemia Iron deficiency Currently on ferrous sulfate 325 mg p.o. daily Depression/bipolar Abilify Sertraline HLD: Atovastatin GERD: Famotidine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chronic fatigue syndrome
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 20.12.2023
- Impfdatum
- 01.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
Reaction to the shot in term of pain in the arm significantly worst then prior shots ON; The initial case was missing the following minimum criteria: no specfic product. Upon receipt of follow-up information on 08Dec2023, this case now contains all required information to be considered valid. This is a spontaneous report received from an Other HCP. A 56-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 01Dec2022 as dose 5 (booster), single (Lot number: GJ6739) at the age of 56 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hashimoto", start date: 1997 (ongoing); "Parathyroid removal", start date: 2010 (unspecified if ongoing); "Constipation" (ongoing); "Known allergies: sulfa" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (DOSE 1, lot number unknown), administration date: 12Mar2021, for COVID-19 immunisation, reaction(s): "Pain in the arm"; BNT162b2 (DOSE 2, lot number unknown), administration date: 01Apr2021, for COVID-19 immunisation, reaction(s): "Pain in the arm"; BNT162b2 (DOSE 3 (booster), lot number: FH8030; route: intramuscular; site: left arm), administration date: 23Nov2021, for COVID-19 immunisation, reaction(s): "Pain in the arm"; BNT162b2 (DOSE 4 (booster), lot number: FP4554; site: left arm), administration date: 06Aug2022, for COVID-19 immunisation, reaction(s): "Pain in the arm". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 01Dec2022, outcome "unknown", described as "Reaction to the shot in term of pain in the arm significantly worst then prior shots ON".; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300414510 Same patient, partial same event, different dose;US-PFIZER INC-202300447636 Same patient/event, different dose;US-PFIZER INC-202300447641 same patient/product, different event/vaccine dose;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Constipation; Hashimoto's disease
- Vorgeschichte
- Medical History/Concurrent Conditions: Parathyroid gland excision; Sulfonamide allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 09.11.2023
- Impfdatum
- 11.11.2022
- Beginn
- 01.08.2023
- Tage bis Beginn
- 263,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Ankle fracture
Blood creatinine
COVID-19
Diuretic therapy
Haemorrhage
Hypophagia
Hypoxia
Open reduction of fracture
Oropharyngeal pain
Pain
Renal impairment
Respiratory symptom
SARS-CoV-2 test positive
Skin wound
Splint application
Wound treatment
Symptomtext
Discharge Physician: DO Primary Care Physician: MD Date of Admission: 8/1/2023 Discharge Date: 8/6/2023 Room Number: 2025/2025-1 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: ARF (acute renal failure) (HCC) [N17.9] AKI (acute kidney injury) (HCC) [N17.9] Trimalleolar fracture, left, closed, initial encounter [S82.852A] Open trimalleolar fracture, left, sequela [S82.852S] COVID-19 virus infection [U07.1] 72-year-old woman with a past medical history of type 2 diabetes, CKD 3, hypertension who presented after being sent home from a recent trimalleolar fracture. Patient had been instructed to follow up outpatient with Orthopedic surgery as an outpatient after she had a splint placed in the emergency department. However, when she returned home the skin broke and she experienced bleeding that soaked through her splint and dressing. When she presented back to the emergency department labs were drawn which revealed a creatinine of 3.11. She was also she COVID positive after describing a few days of body aches, sore throat, upper respiratory symptoms. She had poor PO intake but had continued to take her home lasix. Pt was hypoxic on arrival, so placed on decadron and remdesivir. Patient was able to be weaned quickly off oxygen and remained on room air for the remainder of her admission. Patient was aggressively fluid resuscitated due to acute kidney injury. She went to the OR on 08/02/2023 for open reduction external fixation of her ankle fracture. Renal function initially improved but not significantly over the course of 2-3 days. Nephrology was contacted on 08/04 who recommended initiation of Lasix diuresis 40 mg IV twice daily as well as an echocardiogram. Patient renal function declined after initiation of diuretics. Patient was transferred to Butterworth for a formal nephrology evaluation. Case was discussed with ortho trauma prior to transfer so they could arrange to follow/evaluation her at the receiving facility. Patient was in agreement with the plan and she was transferred in stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hyperlipidemia associated with type 2 diabetes mellitus Essential hypertension Peripheral polyneuropathy History of endometrial cancer Hypothyroidism Moderate nonproliferative diabetic retinopathy of both eyes with macular edema associated with type 2 diabetes mellitus (HCC) Lumbar back pain Gastroesophageal reflux disease without esophagitis Type 2 diabetes mellitus, without long-term current use of insulin (HCC) Normocytic anemia Elevated lipase Bilateral edema of lower extremity Hypoalbuminemia Abnormal weight gain RUQ abdominal pain Iron deficiency anemia secondary to inadequate dietary iron intake Stage 3a chronic kidney disease (HCC) CVA (cerebral vascular accident) (HCC) AKI (acute kidney injury) (HCC) Bacteremia due to Enterococcus Physiologic anisocoria Pseudophakia Hypermetropia Refractive amblyopia Regular astigmatism Acute urinary retention Skull lesion Monoclonal gammopathy Acute blood loss anemia Multiple myeloma (HCC) Unspecified severe protein-calorie malnutrition (HCC) S/P BKA (below knee amputation) unilateral, left (HCC)
- Andere Medikamente
- acetaminophen (TYLENOL) 500 mg tablet aspirin 81 mg chewable tablet atorvastatin (LIPITOR) 40 MG tablet calcium carbonate (TUMS) 1,000 mg chewable tablet clotrimazole (LOTRIMIN) 1 % cream ferrous sulfate 325 (65 Fe) MG delayed release table
- Allergien
- MilkDiarrhea Robitussin [Dextromethorphan]
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 28.07.2023
- Impfdatum
- 12.11.2022
- Beginn
- 01.02.2023
- Tage bis Beginn
- 81,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Urticaria
Urticaria chronic
Symptomtext
As has happened after every Covid vaccine I've received, approximately two months after the injection I broke out in chronic hives which lasted for months. This time, the hives weren't confined to my face and neck, but covered my entire body, requiring trips to doctors and dermatologists. I have made several reports to the VAERS site, and I have never received a response. Except for one dermatologist, none of my doctors acknowledged chronic spontaneous urticaria as a potential side effect of the vaccine. I see now that several studies have documented a link, which I hope will inspire researchers to explore this serious side effect.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multi-vitamin, Hydrochlorothiazide, doxycycline
- Allergien
- Latex, sulfa drugs (perhaps), molds
- Vorherige Impfungen
- site swelling and lumps for TDAP, flu, etc. when vials with latex stoppers were used
- Staat
- NC
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 12.06.2023
- Impfdatum
- 18.10.2022
- Beginn
- 08.06.2023
- Tage bis Beginn
- 233,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pain
Injection site swelling
Joint range of motion decreased
Symptomtext
Site: Swelling at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 06.06.2023
- Impfdatum
- 17.05.2023
- Beginn
- 18.05.2023
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
Arthralgia
Bone pain
Brain fog
Chills
Headache
Hyperglycaemia
Malaise
Myalgia
Oral discomfort
Prostatitis
Pyelonephritis
Pyrexia
SARS-CoV-2 test negative
Testicular pain
Urinary retention
Symptomtext
Myalgias, arthralgias, bone pain, and testicular pain for 10 days Fever, chills, malaise, and intermittent profuse sweating for 7 days Loss of sense of taste and smell persistent to present Fatigue and intermittent dyspnea, persistent to present Hyperglycemia for 2 weeks Low grade constant headache and mental fogginess for 10 days Sensation of burning on inspiration inside of oral cavity for 10 days Intermittent urinary retention x 2 weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- 5,0
- Labordaten
- Covid-19 multiple home testing and hospital test negative Hospitalized for Pyelonephritis wiht prostatitis to R/O Sepsis
- Aktuelle Erkrankungen
- Type II DM HTN Mixed Hyperlipidemia OSA Asthma Allergic rhinitis due to pollen
- Vorgeschichte
- Same as above
- Andere Medikamente
- Fish oils 1 gm oral BID
- Allergien
- ACE-I cough
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 23.05.2023
- Impfdatum
- 12.10.2022
- Beginn
- 19.11.2022
- Tage bis Beginn
- 38,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Memory impairment
SARS-CoV-2 test positive
Symptomtext
I felt so exhausted, I was almost nonfunctioning, I practically fell into bed. The next morning, I took a home COVID-19 test that came back positive. I called to have a telehealth visit to let my doctor know that I tested positive for CVOID-19. I was prescribed the antiviral Paxlovid that I was able to start that day. This is the second time I have had COVID-19, it seemed to hang on longer this time. It took a week and a half before I really felt like I wanted to get out of bed. I feel like I have long haul COVID-19 symptoms, my memory is foggy, I am more fatigued than I ever was before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 20NOV2022 Home COVID-19 test - positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Asthma; Diabetes; Fibromyalgia; Chronic Fatigue
- Andere Medikamente
- Vitamin D; Insulin
- Allergien
- Tylenol; Tree Pollens; Outdoor Molds; Cat Dander
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 21.05.2023
- Impfdatum
- 30.11.2022
- Beginn
- 27.03.2023
- Tage bis Beginn
- 117,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Back pain
Bone cancer metastatic
COVID-19
Cancer pain
Constipation
Culture stool negative
Diarrhoea
Lung cancer metastatic
Metastatic neoplasm
Neoplasm malignant
Pain
Pain in extremity
Polymerase chain reaction negative
SARS-CoV-2 test positive
Symptomtext
Patient is a 69 y.o. male with a history of untreated metastatic lung CA, recent admission 3/17/23-3/25/23 with low back pain found to have new met to the sacrum and discharged on pain control who presented to RMH 3/27/2023 with worsening cancer related pain. Recommended outpatient radiation once COVID-19 isolation completed. Discharged to home w/ HHC 3/31/23. 1. Cancer Related Pain: recent admission for same in setting of newly found mets in known metastatic diease. Presented with recurrent low-back and right calf pain. Continued home po morphine. Increased Gabapentin, continued Robaxin, continued Decadron, Ativan. Restarted sch Tylenol. VIR and RadOnc followed. Plan for OP radiation for further pain control. 2. COVID-19 Infection : s/p vaccination x3 (Pfizer). Denied with fever, general malaise. Symptom onset ~3/24/23, Positive test 3/27/2023. Intermittent LFNC requirements on admission. Discontinued remdesivir 3/29/23. Continued decadron as above. Stable on room air. 3. Acute Diarrhea: suspected secondary to bowel regimen/medication induced following recent prolonged episode of constipation. Stool PCR negative. Supportive care. 4. Metastatic NSCLC of RUL: (Dx 2019). Follows with Dr (Oncology). Recommended radiation at time of diagnosis, however declined treatment and later lost to follow-up. Recent admission as above, found to have new metastasis to sacrum, discharged with plans for outpatient follow-up with radiation oncology. Awaiting scheduling for outpatient full body scan. Oncology navigator followed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 17.05.2023
- Impfdatum
- 04.10.2022
- Beginn
- 08.05.2023
- Tage bis Beginn
- 216,0
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Headache
SARS-CoV-2 test
Symptomtext
headache like if had been in a 10-round boxing match; I have COVID; I have COVID; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team and product quality group, Program ID: 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 04Oct2022 as dose 5 (booster), single (Lot number: GJ6739) at the age of 76 years, in arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 29Jan2021 as dose 1, single (Lot number: EL9265), in left arm, on 19Feb2021 as dose 2, single (Lot number: EN6201), in arm, on 05Oct2021 as dose 3 (booster), single (Lot number: FE3590), in arm and on 11Apr2022 as dose 4 (booster), single (Lot number: FK9895), in arm for covid-19 immunisation. The patient's relevant medical history included: "Arthritis" (unspecified if ongoing), notes: Arthritis Diagnosed for 2 years. Had full hip, replacement surgery 2 years ago, on the left hip.; "hip replacement surgery" (unspecified if ongoing), notes: Arthritis Diagnosed for 2 years. Had full hip replacement surgery 2 years ago, on the left hip. There were no concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 08May2023, outcome "recovered" and all described as "I have COVID"; HEADACHE (non-serious), outcome "recovering", described as "headache like if had been in a 10-round boxing match". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (08May2023) Positive, notes: Positive for COVID-19: Sunday night or Monday night she went and got tested. Results came in Monday night, 08May2023. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient was just prescribed. The patient had COVID and received all the 5 Pfizer shots and booster, so much for that. With that said, the Doctor, he prescribed her Paxlovid, he had only taken it for a day, but he noticed this morning a terrible taste in the mouth, that taste terrible, she brushed her teeth, and it did not go away. She was just curious, she knew it was a new thing, under emergency, she was 76 and healthy, but COVID was just nasty, it's just nothing she was fine, she was located, in (withheld). She had a "unintelligible" headache like if had been in a 10-round boxing match, this was her 4th day and she was feeling better, but had her covid test; her Doctor called, and was shocked. She was still use mask and everything, and she got vaccinated, she did not have a problem, not even a sore arm. The caller mentioned she took her adult son to the ER due to a burn, and there were a lot of people in the ER without masks, so she believed that's where they got infected, because her son was also sick. The caller also added that caller had body aches, and 8 out of 10 of the symptoms. The caller mentioned she also had a little bit of loose stool and asked if this a side effect from the medication as well. The caller mentioned she had been eating before taking the 3 pills as recommended by her Doctor. The caller was prescribed with Paxlovid after getting Covid. She was also wondering why she had Covid after having 5 Pfizer Vaccines. She mentioned that after taking Paxlovid, she's had a metallic taste in her mouth and just wanted to know if that is one of the symptoms and was just curious about it. Stated she wasn't complaining, she was just curious. Hasn't previously had COVID-19, but has it now. She had her boosters for the COVID-19 Vaccines. She's 76 years old. At this end game, she thought she wouldn't get COVID-19. But she was so sick and didn't think it was COVID. They ran the test at urgent care and her doctor called telling her she has COVID-19. only been on Paxlovid for a day, has taken 6 pills. Terrible taste in the mouth: Reiterates it's just a bad taste in the mouth She took her first three Paxlovid pills last night, 09May2023. COVID-19 Vaccine: Positive for COVID-19: Sunday night or Monday night she went and got tested. Results came in Monday night, 08May2023. But caller didn't noticed the results until she saw the email Tuesday morning, 09May2023. Her doctor called in Paxlovid and then albuterol for wheezing. Doesn't know if wheezing is part of the COVID-19. She had wheezing before she began taking Paxlovid, she thinks it's part of COVID-19. It's horrible wheezing and her doctor ordered a chest x-ray. All 5 COVID-19 Vaccines she received were manufactured by Pfizer. Vaccine information is provided by caller's COVID-19 Vaccine card. Dose amount is unknown for all 5 vaccines. The sample of the product available to be returned, if requested: Not provided. The packaging sealed and intact. As part of the LOE simplification process, the following Complaint Records were classified as Product Use Attributes // Lack of Effect and have been moved to Closed (No Investigation) state referencing a previously completed investigation for the same product and lot as per the 'One and Done' business process according to in PQS Q1215 and/or Q1252. Conclusion of Previously Completed Investigation for Lots # (CR): EL9265, EN6201, FE3590, FK9895 and GJ6739: The complaint for lack of effect of the Pfizer biontech Covid-19 vaccine lot EL9265, EN6201, FE3590, FK9895 and GJ6739 was investigated. The investigation included a review of manufacturing and packaging batch records, deviation investigations, and an analysis of complaint history for the reported lot and product type. The final scope included the reported finished goods lot EL9265, fill lot EL9256, and the formulated drug product lot EL9247; the reported finished goods lot EN6201, fill lot EN5333, and the formulated drug product lot EN5322; the reported finished goods lot FE3590, fill lot FA9134, and the bulk formulated drug product lot FE5064; the reported lot FK9895; the finished goods lot GJ6739, bulk and fill lots, GJ6726, and GJ6733. A complaint sample was not returned. No related quality issues were identified during the investigation. There is no impact on product quality, regulatory, validation and stability. (Withheld) concludes that the reported defect is not representative of the quality of the batch and the batch remains acceptable. The process determined that no regulatory notification was required. The reported defect could not be confirmed. No root cause or CAPA were identified as the complaint was not confirmed. No corrective or preventative actions were identified because it was determined that the controls in place were sufficient at preventing and removing defects that could cause a complaint of this nature. All release testing performed prior to the release of the reported batch was within specifications.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300187833 same reporter/patient/product, different dose/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230508; Test Name: COVID-19 Test; Test Result: Positive ; Comments: Positive for COVID-19: Sunday night or Monday night she went and got tested. Results came in Monday night, 08May2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arthritis (Arthritis Diagnosed for 2 years. Had full hip replacement surgery 2 years ago, on the left hip.); Hip replacement (Arthritis Diagnosed for 2 years. Had full hip replacement surgery 2 years ago, on the left hip.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 15.05.2023
- Impfdatum
- 10.12.2022
- Beginn
- 15.04.2023
- Tage bis Beginn
- 126,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose
Blood glucose increased
COVID-19
Frequent bowel movements
SARS-CoV-2 test
Fatigue
Hypersensitivity
Malaise
Pain
SARS-CoV-2 test positive
Sneezing
Vaccination failure
Symptomtext
I had my vaccination on 12/10/2022. I started to feel unwell on 04/15/2023 to include symptoms of sneezing and allergies. I woke up on 04/16/2023 with body aches and fatigue. I tested COVID-19 Positive on 04/16/2023. I was prescribed Paxlovid. I still feel unwell on 05/15/2023. I did have COVID-19 on 07/04/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 04/16/2023 test COVID-19
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; Type II Diabetes
- Andere Medikamente
- Januvia; Losartan
- Allergien
- Smoke
- Vorherige Impfungen
- COVID-19 Vaccinations 1 & 2; Swollen at injection site.
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 15.05.2023
- Impfdatum
- 10.12.2022
- Beginn
- 15.04.2023
- Tage bis Beginn
- 126,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose
Blood glucose increased
COVID-19
Frequent bowel movements
SARS-CoV-2 test
Fatigue
Hypersensitivity
Malaise
Pain
SARS-CoV-2 test positive
Sneezing
Vaccination failure
Symptomtext
I had my vaccination on 12/10/2022. I started to feel unwell on 04/15/2023 to include symptoms of sneezing and allergies. I woke up on 04/16/2023 with body aches and fatigue. I tested COVID-19 Positive on 04/16/2023. I was prescribed Paxlovid. I still feel unwell on 05/15/2023. I did have COVID-19 on 07/04/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 04/16/2023 test COVID-19
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; Type II Diabetes
- Andere Medikamente
- Januvia; Losartan
- Allergien
- Smoke
- Vorherige Impfungen
- COVID-19 Vaccinations 1 & 2; Swollen at injection site.
- Staat
- OR
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 10.05.2023
- Impfdatum
- 25.10.2022
- Beginn
- 22.04.2023
- Tage bis Beginn
- 179,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Influenza virus test negative
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test negative
Symptomtext
In late April 2023 I had a very sore throat, and it lasted several days. I had a telehealth visit. I began taking amoxicillin. I had another visit with an in-person doctor. I tested negative for COVID-19 and the flu. After another 5 days I began to feel better but fatigued and a bit congested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19, negative, 04/29/2023; Influenza, negative, 04/29/2023
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes; High Cholesterol; Hypothyroidism; High Blood Pressure; Back Bulging Disc
- Andere Medikamente
- Tejero; Humalog; Trulicity; Metformin; Irbesartan; Chloreglidone; Atorvastatin; Gabapentin; Multi Vitamin; Flonase; Fish Oil; Benfoeimine; Iron; Aspirin; Aleve
- Allergien
- Lisinopril
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 10.05.2023
- Impfdatum
- 09.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy kidney abnormal
Blood test abnormal
Blood urine present
Chills
Fatigue
Headache
IgA nephropathy
Protein total increased
Pyrexia
Vomiting
Symptomtext
The day after the booster I had fever, headache, chills and vomiting. I then had blood in my urine. I went to the doctor several days later. I have had several blood tests and a kidney biopsy. I had high protein levels in my blood and learned that I have IGA nephropathy. My symptoms have gotten better but I am fatigued. There is no treatment. My flare up seems to have gotten better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- 2,0
- Labordaten
- Kidney Biopsy, IGA nephropathy, 04/2023; Blood panels, abnormal, 01/2023
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Crohn's Disease; Migraines
- Andere Medikamente
- LIPITOR; propranolol; ENTIVIO
- Allergien
- Sulfa; FLAGYL; REMICADE; HUMIRA
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 08.05.2023
- Impfdatum
- 14.04.2023
- Beginn
- 14.04.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Overdose
Pain
Symptomtext
extreme body pain especially in the upper part of his body; Chills; Fatigue; nurse administered 0.5ml of the vaccine as opposed to 0.3ml; This is a spontaneous report received from a contactable reporter(s) (Other HCP). A 53-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Apr2023 as dose 3 (booster), 0.5 ml single (Lot number: GJ6739, Expiration Date: 31Jul2023) at the age of 53 years, in left deltoid for covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (Dose 1), for Covid-19 immunization; Covid-19 vaccine (Dose 2), for Covid-19 immunization. The following information was reported: OVERDOSE (medically significant) with onset 14Apr2023, outcome "not recovered", described as "nurse administered 0.5ml of the vaccine as opposed to 0.3ml"; CHILLS (medically significant) with onset 15Apr2023, outcome "not recovered"; FATIGUE (medically significant) with onset 15Apr2023, outcome "not recovered"; PAIN (medically significant) with onset 15Apr2023, outcome "not recovered", described as "extreme body pain especially in the upper part of his body". Caller is a nurse practitioner calling about the Covid-19 Bivalent vaccine and reported that on the 14Apr2023, one of their nurse administered 0.5ml of the vaccine as opposed to 0.3ml. The patient initially felt fine, but 24 hours later, they complained about extreme body pain especially in the upper part of his body. Caller stated that they were body aches. The patient had no fever, but has chills and fatigue and is still experiencing all of this and reporting that it is the same or worse. Relatedness of drug to reaction(s)/event(s): Source of assessment: Method of assessment: Result of Assessment: Yes; Sender's Comments: As there is limited information in the case provided, the causal association between the reported events and the suspect drug BNT162B2 cannot be excluded. The case will be reassessed once new information is available. The impact of this report on the benefit/risk profile of the Pfizer drug 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
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 04.05.2023
- Impfdatum
- 27.10.2022
- Beginn
- 30.01.2023
- Tage bis Beginn
- 95,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
COVID-19
Cough
Fatigue
Nasopharyngitis
Oropharyngeal pain
SARS-CoV-2 test positive
Sensation of foreign body
Somnolence
Wheezing
Symptomtext
1/30/23 I woke up with a real bad sore throat. I thought I had a cold. I went to the clinic and was tested for COVID and it came back positive a few days later. I lost my sense of taste and smell. I was very sleepy and exhausted. I went to the clinic and was prescribed Paxlovid. Within a day and a half of taking it, I felt much better. By 2/6/23 I felt better and the next day I got my sense of smell and taste back. Every once in a whle, I will still get something in my throat, like mucous. Sometimes something comes up and sometimes it does not. If I don?t take a cough drop, I will have a coughing fit. I also feel like I am wheezing every once in a while.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 2FEB23-COVID Test-Positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Extreme Dry Eye, Diverticulosis , High Blood Pressure, High Cholesterol
- Andere Medikamente
- Lisinopril, Simvastatin, Vitamin D2, Low Dose Aspirin
- Allergien
- Iodides,Penicillin
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 03.05.2023
- Impfdatum
- 26.10.2022
- Beginn
- 26.12.2022
- Tage bis Beginn
- 61,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I started with a low grade fever and a cough. The cough got worse and was worse at night. I took some over the counter symptomatic relief. I called my doctor. He prescribed Paxlovid. We picked it up the next day. The cough hung on at least two more nights. I generally felt better after taking the Paxlovid. After the fourth or fifth day, I felt like I was pretty much over it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- 12/26/2022 At Home COVID-19 Test - Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure; High Cholesterol; Chronic Heartburn; Constipation
- Andere Medikamente
- Lisinopril HCTZ; Amlodipine; Atorvastatin; Famotidine; Low Dose Aspirin; Magnesium; Multivitamin; Calcium Plus Vitamin D3; Vitamin C; Docusate Sodium
- Allergien
- Gabapentin; Benzoin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 02.05.2023
- Impfdatum
- 28.10.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 4,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Pruritus
Scratch
Symptomtext
Started itching in Nov. Dermatographia occurs with scratching itchy areas. Itching has continued since shot. Saw allergy doctor and she hade change allergy medicine to Zyrtec. I'm taking 30 mg daily with intermittent improvement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraine, seasonal allergies
- Andere Medikamente
- Topamax, Allegra, singular, fish oil, B2, D3
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 02.05.2023
- Impfdatum
- 20.10.2022
- Beginn
- 22.12.2022
- Tage bis Beginn
- 63,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose increased
COVID-19
Decreased appetite
Dizziness
Fatigue
Feeling abnormal
Influenza like illness
SARS-CoV-2 test positive
Symptomtext
I had flu like symptoms. I was very tired. I was dizzy and had loss of appetite. The reason why I went to the doctor was because it was carrying on a long time. He suggested that it might have been long COVID-19 that I had. I did take a home COVID-19 test that came back positive. Between 30 to 40 days later I'm still having the same symptoms. In all I have taken about three tests between December and February. I saw my primary care physician in January and my blood sugar was elevated for no reason. I haven't felt like myself since I had that last shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- 12DEC2022 COVID-19 test - positive; JAN2023 COVID-19 test - Negative; FEB2023 COVID-19 test - Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High blood pressure; Controlled Cholesterol
- Andere Medikamente
- Amlodipine; Metoprolol; Rosuvastatin; Gabapentin; Celecoxib; Tylenol
- Allergien
- Chicken
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.05.2023
- Impfdatum
- 02.12.2022
- Beginn
- 30.03.2023
- Tage bis Beginn
- 118,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Myalgia
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
My symptoms started on 3/30/2023 which started in the morning. I was coughing, congested, fatigue and sore all over on my muscles. I had sore throat and did not have a fever. This was 3 days. On 3/31/2023 I called the telehealth and the nurse practitioner have me PAXLOVID. The symptoms improved by 4/3/23 and on 4/4/23 I felt normal. On the 4/6/23. I tested negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 3/30/2023 COVID-19 positive; 4/6/2023 COVID-19 negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes Type 2
- Andere Medikamente
- Multivitamin; ZYRTEC; metformin; rosuvastatin; MOUNJARO injection
- Allergien
- Seasonal; cats
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 27.04.2023
- Impfdatum
- 25.10.2022
- Beginn
- 07.03.2023
- Tage bis Beginn
- 133,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test normal
Electrocardiogram normal
Headache
Urine analysis normal
Symptomtext
My adverse event started on 03/07/2023 in the afternoon. I had a headaches which was 8/10 in a scale. I took Tylenol but it didn't go away. I had a high blood pressure which was 220/110. I called my doctor in the afternoon around 1:00pm because of the headaches since, his office was booked up I wasn't able to see him. On 03/09/2023 I went to the Urgent Care they did full Blood Work, EKG, and Urine test. EKG was normal. The doctor prescribe me Amlodipine 5 mg. I also did a follow up on 03/11/2023 my headaches were gone and blood work / urine test came out to be normal. He told me to call my doctor and follow up with him within 1-2 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 09MAR2023 Blood Work Test- Normal; 09MAR2023 EKG - Normal; 09MAR2023 Urine Test- Normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Thyroid Issues; Overactive Bladder; High Cholesterol; Dry Eye
- Andere Medikamente
- Multivitamins; Omega 3; Vitamin D; Levothyroxine; Atorvastatin; Darifenacin
- Allergien
- Tetracyclines; Penicillin; Restasis
- Vorherige Impfungen
- Shakes, chills and fever with all COVID-19 Vaccines
- Staat
- AZ
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 25.04.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.03.2023
- Tage bis Beginn
- 151,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Chills
Cough
Headache
Malaise
Nausea
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I got sick on the 12, I took the test, and it was negative; on the 13th very sick, I took another test, and it was positive. I called my doctor; I spoke to him on the 14th. I had really bad headache, nausea, chills, very weak, a fever was very low, 99, plus I had a cough and congestion. I gave the doctor my symptoms and he gave me anti-virus and started taking it on the 14th.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 12MARCH2023 COVID-19 test negative; 13MARCH2023 COVID-19 test positive; 20MARCH2023 COVID-19 test negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Amlodipine; NP thyroid; baby aspirin; chromium picolinate; cranberry vitamins; turmeric; evening primrose oil; fish oil; vitamin C; multivitamins; AZO
- Allergien
- BENADRYL injection
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 21.04.2023
- Impfdatum
- 26.09.2022
- Beginn
- 29.01.2023
- Tage bis Beginn
- 125,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Malaise
Nasal congestion
Pyrexia
SARS-CoV-2 test positive
Sleep disorder
Symptomtext
On the 29th of January, I woke at the middle of the night, with 99 1/2 fever, I did not feel so good, it was Sunday, the whole day I did not feel good, I had 100.5 fever at the most, the following Monday on the 30th, I called and made an appointment with my doctor. On the afternoon I still had a fever 0f 100.5, no sore throat, very mild symptoms, stuffy nose, I took the Covid-19 test Monday and it was positive. The doctor wanted to wait to see how I was doing before prescribed PAXLOVID, two days later I was doing better. I only experience fatigue, feeling tired, but after 10 days it was gone, and it was fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 30JAN2023 COVID-19 test positive; 01FEB2023 COVID-19 test positive; 05FEB2023 COVID-19 test positive; 10FEB2023 COVID-19 test negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin D
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 07.10.2022
- Beginn
- 01.02.2023
- Tage bis Beginn
- 117,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Dizziness postural
Hypersensitivity
Hypoacusis
Ocular discomfort
Paranasal sinus hypersecretion
Vertigo
Symptomtext
I early February I had pressure behind my eyes, muffled ears. It felt like I was having some sinus drainage issues, yet it didn't feel like a sinus infection. I started experiencing extreme dizzy sensation in my head, it felt as if when I moved my head it would take a moment for brain to move. I went to a local pharmacy and discovered I had vertigo caused by allergies. I was advised by the pharmacist to try ZYRTEC to clear my allergies. Within the hour of taking the ZYRTEC my symptoms were cleared, it did take five days for the vertigo to be completely gone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetic
- Andere Medikamente
- CENTRUM multivitamin; metformin; LIPITOR; horse chestnut
- Allergien
- Lisinopril; grass; latex
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 18.04.2023
- Impfdatum
- 26.10.2022
- Beginn
- 18.04.2023
- Tage bis Beginn
- 174,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I tested positive for COVID-19 on 3/12/23. I had congestion, body aches, and a low-grade fever. I contacted my doctor and was prescribed Paxlovid. I felt better in a few days. It was a very mild case.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- 12MAR2023 COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; High Cholesterol; Gout
- Andere Medikamente
- Rosuvastatin; Amlodipine; Allopurinol
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 17.04.2023
- Impfdatum
- 27.09.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 92,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Headache
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I started experiencing sore throat, tiredness, fever, and headache on 12/28/2022 in the morning. I took COVID-19 home test on 12/27/2022 which was negative. On 12/28/2022 I took another COVID-19 test which was positive. I took COVID-19 12/31/2022, 01/01/2023- positive. On 01/05/2023 COVID-19 home test was faint. On 01/07/2023 and 01/08/2023 which was negative. I didn't call my doctor I just treated it as a cold. I took over the counter Vitamin C, Zinc and Tylenol as per needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 28DEC2022 COVID-19 Test- Positive; 31DEC2022 COVID-19 Test- Positive; 01JAN2023 COVID-19 Test- Positive; 07JAN2023 COVID-19 Test- Negative; 08JAN2023 COVID-19 Test-Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes; Environmental Allergies; Seasonal Allergies
- Andere Medikamente
- N/A
- Allergien
- Latex; Egg Plants; Shellfish; Perfume; Crab
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 14.04.2023
- Impfdatum
- 13.10.2022
- Beginn
- 10.04.2023
- Tage bis Beginn
- 179,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Feeling hot
Lymphadenopathy
Oropharyngeal pain
Pain
Rhinorrhoea
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
I had a fever of 99.7 and body aches and coughing and sore throat swollen glands. Running nose. COVID-19 was positive. Doctor gave me PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 08APR23 PCR test negative 11APR23 home COVID test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- CRESTOR; propranolol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 14.04.2023
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Dizziness
Headache
Magnetic resonance imaging spinal abnormal
Spinal disorder
Symptomtext
After the vaccine, I had a headache, I felt off balance, my joints hurt. The headache I have, it's chronic and I am dizzy. Some days are mild, other days are very bad, both headache & dizziness. Every month I see the doctor, he said he thinks is a vaccine related and he gives me medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- 01FEB2023 MRI Cervical problem
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Psoriatic Arthritis
- Andere Medikamente
- Raloxifene; estradiol vaginal cream; vitamin C; vitamin D; lutein; turmeric; calcium
- Allergien
- Erythromycin; levofloxacin; iodine; famciclovir; trazodone; terbinafine; tizanidine; duloxetine; gabapentin; propranolol
- Vorherige Impfungen
- COVID-19 dose 2; 2021; I had fever at night, hurt at the arm, all my joints ached during the night and headache. The headache, I
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 13.04.2023
- Impfdatum
- 25.10.2022
- Beginn
- 21.03.2023
- Tage bis Beginn
- 147,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aphonia
Brain fog
COVID-19
Cough
Fatigue
Paranasal sinus discomfort
SARS-CoV-2 test positive
Sinus headache
Symptomtext
3/21/2023 Woke up with a severe cough, fatigue and an on again off again sinus pressure headache. Tested with At Home COVID-19 test, positive. 3/22, coughing severely and loss of voice. 3/23 Televisit with Doctor who proscribed Paxlovid, Prednisone, and Promethazine DM. Doctor recommended albuterol, but allergist recommended increased dose of Symbicort. Coughing subsided by the weekend, 3/25. Symptoms gradually diminished until 3/25, but the fatigue lingered another week. Brain Fog lingers to the time of reporting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 21Mar2023 At Home COVID-19 test, positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma; Bronchitis
- Andere Medikamente
- Symbicort; Montelukast; Celebrex; Cevimeline; Nexium; Famotidine; Amlodipine; Rosuvastatin; Flonase Allegra; Latanoprost
- Allergien
- NA
- Vorherige Impfungen
- ALL COVID-19 vaccines caused loss of voice for a few days.
- Staat
- VA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 12.04.2023
- Impfdatum
- 04.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Plasma cell myeloma
Pyrexia
Symptomtext
I was diagnosed with Myeloma on March 15, 2023. My symptoms started on October 5, 2022 I experienced fatigue, occasional low grade fever, I was taking MOTRIN for my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Myeloma
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 12.04.2023
- Impfdatum
- 11.10.2022
- Beginn
- 23.03.2023
- Tage bis Beginn
- 163,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Brain fog
COVID-19
Chills
Confusional state
Cough
Dizziness
Fatigue
Feeding disorder
Insomnia
Nausea
Oropharyngeal pain
Oxygen saturation decreased
Respiratory tract congestion
Retching
SARS-CoV-2 test positive
Symptomtext
1.mild sore throat started on 3/20/23- 2. extreme sore throat, chills, brain fog, dizziness, nausea, fatigue on 3/23/23 3. 3/23/23 called Dr.'s office to get treatment., I was told the doctor does not treat covid. I asked what should I do, they said it was like the common cold. I asked how long should I isolate and they told me they did not know the recommendations at this time and laughed. They told me to rest and look up isolation recommendations on line. 4. 3/24 symptoms became worse, extreme nausea, dizziness, fatigue, non stop chills, sore throat was so bad I was gagging on spit in my sleep. Difficult sleepy and confusion. blood ox was down from 99 to 95. 5. 3/25 My neighbor who is a doctor prescribed paxlovid. I did not go to a doctors office. They called it in to. a pharmacy and picked it up for me. blood ox was 95. Could not eat. Fluid and popsicles. Ate a little rice. 6. 3/26 blood ox was ranging from 90-95. Nieghbor doctor advised I go to ER. Blood ox was increased at ER up to high 90s. They sent me home and told me to continue paxlovid. Very confused, worst sore throat of my life, chills would not stop, nausea was very bad could not eat. Only drinking fluids and popsicles. Ate rice and apple sauce. Slept on and off for 18 hours. 7. 3/27 Similar symptoms to 3/26, blood ox was higher 98 -99. tested positive for 9 days. I am on week 3 still light headed, coughing and congestion with brain fog.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- home covid tests - positive 3/23 home covid test -positive 3/28 home covid test -positive 3/29 home covid test -positve 3/30 home covid test -negative 3/31 home covid test -negative 4/1
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none-history of asthma. not active currently or at time of vaccinations.
- Andere Medikamente
- sleep aid yogi sleepy time tea Motrin
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 09.10.2022
- Beginn
- 13.01.2023
- Tage bis Beginn
- 96,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Influenza like illness
Malaise
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
01/13/2023 I started having a fever, sore throat and flue like symptoms. After reaching out to my doctor I was diagnosed with Covid. I was prescribed Paxlovid. Symptoms lasted a week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Covid-19 test- Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Multivitamin; Calcium; Doxepin; Alendronate
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 10.04.2023
- Impfdatum
- 07.10.2022
- Beginn
- 27.02.2023
- Tage bis Beginn
- 143,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
I had a sore throat, congestion, and a headache. I contacted my doctor and was prescribed amoxicillin. I also took ibuprofen. I decided to take a COVID-19 test because I had a dentist appointment and I ended up testing positive. I contacted my doctor but was not prescribed medication. I took another COVID-19 test on day 10 and tested negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 01MAR2023 COVID-19 test positive; 11MAR2023 COVID-19 test negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Cholesterol
- Andere Medikamente
- Ibuprofen; fish oil; calcium; vitamin D
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 10.04.2023
- Impfdatum
- 17.10.2022
- Beginn
- 28.01.2023
- Tage bis Beginn
- 103,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Infection
Nasopharyngitis
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I did not have an adverse reaction to the vaccine. I had a runny nose and just thought I was getting a cold. I tested positive for COVID-19 on 01/28/2023 with extreme fatigue. I talked to my doctor, and I was offered the prescription for Paxlovid but I declined. I did have three separate infections after I recovered from COVID-19. I was on three separate antibiotics. As of today, I am feeling better with no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 28JAN2023 COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- AFIB; Hashimoto's disease; Asbestos
- Andere Medikamente
- Melatonin; Multivitamin; Vitamin D; CoQ10; Probiotic; Magnesium; Antihistamine; Medical Marijuana
- Allergien
- Statins; Oxycodone
- Vorherige Impfungen
- Tetanus vaccine, around 2003, the injection site was swollen and infected.
- Staat
- PA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 07.04.2023
- Impfdatum
- 10.10.2022
- Beginn
- 12.02.2023
- Tage bis Beginn
- 125,0
- Dosis
- 5
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bladder discomfort
Bladder disorder
Bladder irritation
Cystitis noninfective
Cystoscopy
Pollakiuria
Pyrexia
Urinary retention
Urinary tract disorder
Urinary tract infection
Urine analysis normal
Urine flow decreased
Symptomtext
2/12/2023 I woke up and realized there was something wrong with my bladder and urinary system. It felt like I was getting a UTI. I went to the bathroom, and nothing was working right. The pressure and frequency got closer together. It felt like a combination of a bacteria and yeast version. I developed a fever and contemplated calling the ambulance. I was taking ibuprofen and the fever broke. 2/13/23 I called the Urologist and spoke with the physician assistant. I went to their office on 2/14/23 and gave a urine sample. I was prescribed an antibiotic that is traditionally prescribed for a new patient developing a Urinary Tract Infection. After 7 days on the antibiotic, on 2/21/23, it was apparent it was not working. I had a little bit of improvement, but in no way cleared it out. I called the doctor's office and told them the medication was not working. They had lost my urine sample from the previous visit. I went into the office to give another sample. I got a message from the doctor who prescribed CIPRO for 10 days and a prescription for after the CIPRO to take for two days. The frequent urination and very slow draining and incomplete draining was still going on, something was wrong. I called the doctor's office and told them it helped, but I was not cured that something else was going on. I had an appointment to see the doctor on 3/7/23. The lab work that came back and showed no infection. The doctor scheduled a cystoscopy. I had the cystoscopy on 3/24/23. There had been so much inflammation and irritation, it was causing the restriction. I was recommended to have an implant procedure, a Uro-Lift. I am scheduled to have that done on April 19, 2023. I am improving.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- 21FEB23 Urine test, no infection; 24MAR23 Cystoscopy inflammation and restriction
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes Type 2; Hyperlipemia; Overweight; Hypertension; Peripheral neuropathy; Osteoarthritis
- Andere Medikamente
- Insulin aspart pump; valsartan HCT; simvastatin; metformin; vitamin D3; baby aspirin; omega 3 fish oil; vitamin C; potassium; fexofenadine; cranberry; cinnamon; chromium picolinate; iron; multivitamin; super B complex vitamin; magnesium; zi
- Allergien
- Liraglutide; dulaglutide
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 07.04.2023
- Impfdatum
- 28.10.2022
- Beginn
- 18.03.2023
- Tage bis Beginn
- 141,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Influenza virus test
Nasopharyngitis
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Streptococcus test
Symptomtext
On Sat March 18 I felt like I was having some head congestion and some fatigue, and I didn't think it was COVID-19. The next day I started to have body aches and fever and that when I figured it was more than just a head cold. I tested for COVID-19 and was positive the following day I went to the local clinic to confirm that I had COVID-19. I was in fact correct that I was positive for COVID-19. I was given a prescription for PAXLOVID. From March 20-24, I started to recover and had zero symptoms left. I took another home test on March 26 I was positive and then again, the next day and was negative. A few days later I tested again and was negative and the only symptoms that I had left were the allergy like symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Flu; Strep; COVID-19
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Asthma
- Andere Medikamente
- CLAIRTIN; FLONASE; amlodipine; losartan; multivitamin; ADVAIR
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 06.04.2023
- Impfdatum
- 05.10.2022
- Beginn
- 13.03.2023
- Tage bis Beginn
- 159,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Nasal congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I tested positive for Covid-19 on March 23, 2023 I experienced stuffy nose, headache, nasal drainage, I was taking a steroid for my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Dye
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 06.04.2023
- Impfdatum
- 14.10.2022
- Beginn
- 28.03.2023
- Tage bis Beginn
- 165,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain lower
Computerised tomogram abdomen abnormal
Diverticulitis
Electrocardiogram normal
Full blood count normal
Lipase normal
Metabolic function test normal
Urine analysis normal
Symptomtext
On March 29, 2023, I went to the ER for pain in the lower right quadrant of my abdomen. I was diagnosed with Acute Diverticulitis. I was released the same night.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain lower
- Hospital-Tage
- -
- Labordaten
- 03/29/2023 CBC - Normal; 03/29/2023 Metabolic Panel - Normal; 03/29/2023 Lipase - Normal; 03/29/2023 UA- Normal; 03/29/2023 EKG - Normal; 03/29/2023 CT Scan Abdomen - Confirmed Diverticulitis
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Lower Back Pain; Diverticulitis; GERD
- Andere Medikamente
- Esomeprazole; Estradiol; Flonase; CoQ10; Probiotic; Multivitamin; Apple Cider Vinegar; Garlique; Red Yeast Rice
- Allergien
- Pollen; Erythromycin; Septra; Augmentin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 05.04.2023
- Impfdatum
- 03.10.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 87,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Diarrhoea
Influenza
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
On 12/29/2022 had a slight cough and runny nose. I also have more frequent diarrhea. I had no treatment or outcomes. I also caught the flu right after for a week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 29DEC2022-COVID-19-Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; Pre-Diabetic
- Andere Medikamente
- Dutasteride; Enalapril Maleate; Hydrochlorothiazide; Omeprazole; Atorvastatin; Metformin; Aline Probiotic; Fluocinonide
- Allergien
- Lactose intolerant
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 04.04.2023
- Impfdatum
- 28.09.2022
- Beginn
- 18.03.2023
- Tage bis Beginn
- 171,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
COVID-19
Chills
Cough
Fatigue
Pain
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
My COVID-19 Infection symptoms started on 03/18/2023 . I had a cough, fatigue, aches, chills, loss of taste , loss of smell, and sinus congestions. I did a home COVID-19 test on 03/19/2023 which was positive. I sent an email on 03/23/2023 to a PA at my work place. She suggested some over the counter medications such as Sudafed, Nasal Spray, and cold & Sinus medication. I still have lingering cough and sinus congestions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 19MAR2023 COVID-19 Test- Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Anxiety; Depression
- Andere Medikamente
- Lexapro; Buspirone
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 03.04.2023
- Impfdatum
- 13.12.2022
- Beginn
- 09.02.2023
- Tage bis Beginn
- 58,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Malaise
Nausea
Paranasal sinus discomfort
Productive cough
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19. The first few days I was nauseated. I had a fever, pressure in my sinuses, and a very bad cough. The cough was very deep and wet. I was coughing up a lot of stuff. The coughing was the most prominent symptom. I was sick for a full week. I was prescribed PAXLOVID. I started to feel better, but then the symptoms came back. I experienced rebound COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- 10Feb2023 COVID-19 test positive; 16Feb2023 COVID-19 test negative; 19Feb2023 COVID-19 test positive; 25Feb2023 COVID-19 test negative
- Aktuelle Erkrankungen
- Osteoarthritis
- Vorgeschichte
- None
- Andere Medikamente
- Omega 3 fish oil; multivitamin; calcium
- Allergien
- Sulfur
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 28.03.2023
- Impfdatum
- 26.09.2022
- Beginn
- 19.03.2023
- Tage bis Beginn
- 174,0
- Dosis
- 5
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Ear pain
Fatigue
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I had an extreme sore throat, earache, runny nose with congestion. I also had fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- at home rapid COVID-19 test- positive 3/19/2023
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Arthritis; Hypertension
- Andere Medikamente
- Prilosec; Losartan; Synthroid; Norvasc; Zocor
- Allergien
- Codeine; Petrocyclein; Nicainoprol
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 28.03.2023
- Impfdatum
- 26.09.2022
- Beginn
- 16.03.2023
- Tage bis Beginn
- 171,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal discomfort
COVID-19
Malaise
Oropharyngeal pain
Paranasal sinus discomfort
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I had no adverse event following the vaccine. I began not feeling well with upset stomach, congestion and just not feeling well. My whole family was sick, and I was the last one to test positive for COVID-19 on 03/16/2023. I contacted my doctor and told her I tested positive, and she said let them know if I got worse. I took over the counter medication to help with my symptoms. As of today, I continue to have sinus pressure and a sore throat, but I test negative for COVID-19. I previously tested positive for COVID-19 in 04/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- 16MAR2023 COVID-19 test positive; APR2022 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 27.03.2023
- Impfdatum
- 23.09.2022
- Beginn
- 23.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Biopsy breast normal
Bone marrow disorder
Breast pain
Full blood count abnormal
Haematoma muscle
Injection site mass
Laboratory test normal
Lymphadenopathy
Mammogram abnormal
Muscle spasms
Pain in extremity
Vaccination site pain
Symptomtext
My arm hurt at the vaccination site, under my arm, and on top of my right breast. After a week it was still hurting. I mentioned it to my doctor and he said sometimes it takes about three months to go away. In December, I was still sore. In January 2023, my breast and under arm were no longer sore but my injection site was still sore. So I went to the doctor for the pain in my arm. The doctor could feel a lump and stated that sometimes at the injection site there will be scar tissue. They told me to massage it and apply heat. That did make it feel better but it still didn't go away. When I went to the doctor a few weeks ago, and they ordered an ultrasound and physical therapy. The next day a different doctor, my regular doctor, said he didn't want me to have physical therapy and he thought I had a hematoma in the muscle. After the ultrasound where they manipulated it, it hurt more and started to cramp. I am concerned that I didn't want it to get worse. I do have a follow-up appointment with my doctor in two months. I was also diagnosed with a bone marrow abnormality about a month after I received my vaccine. The ultrasound lady said she did see a hematoma in the muscle of my arm. I was also diagnosed with a lymph node in my breast that was larger than it was during my mammogram last year.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast pain
- Hospital-Tage
- -
- Labordaten
- 27SEP2022 CBC Labs, normal; 24OCT2022 CBC Labs, bone marrow abnormality; 26JAN2023 tested for multiple myeloma, negative; 07FEB2023 Mammogram, lymph node in left breast larger than previous year and ordered a needle biopsy; 22FEB2023 needle biopsy, normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Asthma; Chronic Liver Condition; Chronic Allergies of grasses; mold; pollen; Primary Biliary Cholangitis Auto-Immune Disease
- Andere Medikamente
- Albuterol; BENADRYL; levothyroxine; omeprazole; amlodipine; ipratropium bromide
- Allergien
- Walnuts; shellfish; sourdough; some antibiotics; morphine; latex; grasses; molds
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 27.03.2023
- Impfdatum
- 24.08.2022
- Beginn
- 01.03.2023
- Tage bis Beginn
- 189,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest discomfort
Chills
Fatigue
Influenza virus test positive
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I had chills, fever, and fatigue. I took an at home COVID-19 test and tested positive. I contacted my doctor and was prescribed 5 days' worth of Paxlovid. I started to feel some pressure in my chest, so I went to the Emergency Room. They ran some test, and I tested positive for COVID-19 and Flu. They prescribed Azithromycin and Benzonatate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 11MAR2023 COVID-19 Test - Positive; 11MAR2023 Flu Test - Positive; 01MAR2023 COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Tachycardia; Osteoarthritis
- Andere Medikamente
- Biotin; Vitamin B12; Cranberry; Calcium; Aspirin; Atorvastatin; Duloxetine; Metoprolol
- Allergien
- Celebrex; Actonel
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 22.03.2023
- Impfdatum
- 20.09.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 103,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Abdominal pain lower
Abdominal pain upper
Ultrasound scan vagina
Urinary tract infection
Urine analysis normal
Symptomtext
I have had lower left abdominal pressure with occasional pain that has not let up in 3 months. It's not debilitating but it is persistent. Occasionally it is accompanied by an ache or pain in my upper left abdomen just above my ribs. I saw a doctor in early February and the pain feels similar to ovulation pain but when it did not go away so I called my doctor. She sent me for further testing. I had a transvaginal Ultrasound which was inconclusive. My doctor did complete a urinalysis test for a UTI, and it was negative. Less than a week later I began having much more severe symptoms and it was determined that I had a UTI. I was prescribed an antibiotic. The medication temporarily lessoned the symptoms but did not make them go away. My physician recommended me schedule an appointment for a Transvaginal Ultrasound which had no findings. A short time later upper abdominal pressure began and would come and go. The provider indicated that she would prescribe something else but I have not been able to make contact to have the medication prescribed. My symptoms have not gotten better so I do plan to follow up with the provider.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain lower
- Hospital-Tage
- -
- Labordaten
- Transvaginal Ultrasound February 23, 2023, normal, inconclusive. Urinalysis test negative February 2023
- Aktuelle Erkrankungen
- Fever and cough 2 weeks prior to vaccine undiagnosed
- Vorgeschichte
- Hashimoto's Disease
- Andere Medikamente
- Levothyroxine; multivitamin; calcium; vitamin B; ADVIL
- Allergien
- Sulfa drugs; loratadine
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 03.03.2023
- Impfdatum
- 21.11.2022
- Beginn
- 25.02.2023
- Tage bis Beginn
- 96,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Feeling abnormal
Nasopharyngitis
Oropharyngeal pain
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I woke up with cold symptoms such as sore throat running, nose, and coughing. On February 25, 20223, I did a home COVID-19 test and it was positive. I took some over the counter multi symptom cold medicine. The symptoms progressed in the evenings to a fever, and body aches. I also experienced brain fog. I had a telehealth visit with my doctor who told me to continue to take my medication and that I wasn't a candidate for the other prescribed antiviral. My symptoms persisted for three days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 25FEB2023 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Thyroid
- Andere Medikamente
- N/A
- Allergien
- Azithromycin; shellfish
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 29.11.2022
- Beginn
- 07.02.2023
- Tage bis Beginn
- 70,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Pain
Pyrexia
SARS-CoV-2 test positive
Sinus congestion
Sneezing
Symptomtext
02/07/2023 I woke up with a fever, sinus congestion, coughing, sneezing exhaustion and body ache. I reached out to my doctor and was prescribed PAXLOVID. Symptoms lasted approx. 7 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Covid-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Doxepin; multivitamin; venlafaxine
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 07.12.2022
- Beginn
- 26.01.2023
- Tage bis Beginn
- 50,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blister
Herpes zoster
Laboratory test
Neuralgia
Pain of skin
Rash
Rash macular
Scab
Skin discolouration
Symptomtext
She got her vaccine, had no problems until 1/26/23 when she noticed that she had a rash on her right shoulder blade. Then the next day she had a bunch of blisters on the shoulder blade. Then it became like 50 blisters and one dense blister and it was on the weekend and within the 2 days by Monday she had a big red blotch and after the blotch it was almost becoming blisters on crack as they forming so fast that the redness turned into them. She has had friends that had shingles before and they said that they had never seen anything like it. She is still recovering from he blisters even though she has recovered from it. It went over her chest, to her armpit, her inner arm, forearm. She went to see her PCP and she gave her a prescription to pick up, the rash proceeded to take over her body and went to the ER and they were going to hospitalize her for 10 days. She was then given Valtrex IV and put her on really strong RX like 1 gram t.i.d. of Valtrex and then Gabapentin for the nerve pain. She had mentioned to her sister that she thought she had singles, and had the shingles vaccine 2 years ago. She is a nurse so she figured it was shingles, and then the PCP gave her medicine and then ER confirmed that she had shingles. They called the infectious disease doctor and treated her with the IV Valtrex and then sent her home on it as well. After she finished the prescription that since it was so severe to let them know if she didn't get rid of the blisters to let them know and she was extended it and now on it prophylactically for 6 months. They have all crusted over and her skin is still healing, still has some tenderness and dark areas on her skin and hoping that is going to lighten up and having nerve pain as well so continues to take the Gabapentin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain of skin
- Hospital-Tage
- -
- Labordaten
- Multiple.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Rheumatoid arthritis.
- Andere Medikamente
- Orencia, Plaquenil, Rumate multivitamin, Vitamin D3, Magnesium, calcium.
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 24.02.2023
- Beginn
- 24.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Erythema
Heart rate increased
Hyperhidrosis
Nervousness
Panic attack
Vomiting
Symptomtext
Patient did not experience a true allergic reactions they had a panic attack. Panic attack symptoms experienced by patient : vomiting, sweating, dizziness, redness develop on the back of neck and parts of face, increased heart rate Patient had a panic attack after receiving vaccine they where nervous of switching to Pfizer from Moderna. Patient stated they want Pfizer but have a fear of needles. After about 10 minutes patient had dizziness and vomiting. We were about to administer Epi pen but patient stopped and stated no its not an allergic reaction. We called 911 and they asked about symptoms while we where on the phone. Patient started to return back to normal within a few minutes and canceled emergency vehicle. Injection site was also checked and patient injection site was clear with not redness or signs or rash Patient was monitored for an additional 30 minutes and patient was back to normal with no symptoms present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- no needed
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 02.10.2022
- Beginn
- 04.02.2023
- Tage bis Beginn
- 125,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Colitis
Computerised tomogram abnormal
Diarrhoea
Diarrhoea haemorrhagic
Irritable bowel syndrome
Rectal haemorrhage
Symptomtext
The evening of February 4, 2023, I started to have abdominal pain. It proceeded to diarrhea. Within two hours, it turned into bloody diarrhea. On February 5, 2023, it was just blood which caused me to seek immediate care by the night of February 6, 2023. I was prescribed FLAGYL. I was told to take it every 8 hours for 10 days. In addition to that, I was given CIPRO 500mg and was told to take one tablet every 5 hours for 10 days. The diagnosis was Colitis with Rectal Bleeding. I have finished treatment, but I'm still experiencing irritable bowel and diarrhea. I am supposed to follow-up with my GI doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- 02/06/2023 CT Scan, Colitis
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Undifferentiated Connective Tissue Disease; Hypertension; History of Brain Bleed
- Andere Medikamente
- Nortriptyline; FLEXERIL; UNITHROID; estradiol; IMITREX; EDARBI; fish oil; vitamin D
- Allergien
- Morphine; colchicine; PLAQUENIL
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 19.01.2023
- Beginn
- 06.02.2023
- Tage bis Beginn
- 18,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Computerised tomogram abnormal
Diverticulitis
Symptomtext
Feb 8 started having severe abdominal pain intermittently, continue Feb 20th when I went to doctor, received cat scan, diagnosed with diverticulitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- Cat Scan 21Feb2023
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Borderline high blood pressure; history mitral-valve collapse
- Andere Medikamente
- Vitamin C; D3; baby aspirin; melatonin; metoprolol; LIPITOR
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 13.02.2023
- Impfdatum
- 08.11.2022
- Beginn
- 16.01.2023
- Tage bis Beginn
- 69,0
- Dosis
- 5
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
SARS-CoV-2 test positive
Symptomtext
On 11/08/2022 I received my Covid-19 vaccine. On 01/16/2023 I started feeling very tired. I did a home test for Covid-19 and was tested positive. After reaching out to my doctor I was prescribed Paxlovid for 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Covid-19
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Nut allergy
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 12.02.2023
- Impfdatum
- 08.02.2023
- Beginn
- 10.02.2023
- Tage bis Beginn
- 2,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Back pain
Diarrhoea
Nausea
Sciatica
Symptomtext
Nausea, stomach pain, diarrhea lasting 30 hours. Severe sciatic nerve pain and back pain continuing through the weekend that still hasn't resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Sciatica, hypertension
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Losartin 100mg
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 10.02.2023
- Impfdatum
- 04.11.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Symptomtext
Arm soreness after received the Pfizer COVID 19 Vaccines; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 65-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 04Nov2022 as dose 5 (booster), single (Lot number: GJ6739) at the age of 65 years for covid-19 immunisation. The patient had no relevant medical history. The patient took concomitant medications. Vaccination history included: BNT162b2 (1st dose, Lot: ER8733, Expiry/NDC: Unknown), administration date: 02Apr2021, when the patient was 63-year-old, for COVID-19 immunization, reaction(s): "arm was sore"; BNT162b2 (2nd dose, Lot: EW0173, Expiry/NDC: Unknown), administration date: 30Apr2021, when the patient was 63-year-old, for COVID-19 immunization, reaction(s): "arm was sore"; BNT162b2 (3rd dose, Lot: FJ8757, Expiry/NDC: Unknown), administration date: 24Nov2021, when the patient was 64-year-old, for COVID-19 immunization, reaction(s): "arm was sore"; BNT162b2 (4th dose, Lot: FJ9943, Expiry/NDC: Unknown), administration date: 12Apr2022, when the patient was 64-year-old, for COVID-19 immunization, reaction(s): "arm was sore". The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 04Nov2022, outcome "recovered" (Nov2022), described as "Arm soreness after received the Pfizer COVID 19 Vaccines". Additional information: There were no prior Vaccinations (within 4 weeks) reported. There was no family Medical History Relevant to Adverse Events (AEs) reported. The patient stated that she takes vitamins. The patient verifies that her arm was sore with all of her Pfizer COVID 19 doses. Stated that if you give her any kind of shot, her arm will hurt. Arm soreness after received the Pfizer COVID 19 Vaccines began the night she received the vaccine and lasted about 2-3 days. No prior Vaccinations (within 4 weeks), no any other vaccinations within four weeks prior to the first administration date of the suspect vaccine. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- 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
- -
- Staat
- AR
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 02.02.2023
- Impfdatum
- 21.12.2022
- Beginn
- 01.02.2023
- Tage bis Beginn
- 42,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Oropharyngeal pain
Pain
Symptomtext
I experienced COVID-19 99.6 fever; sore throat; body aches; & chills I am currently taking ibuprofen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 05.01.2023
- Beginn
- 30.01.2023
- Tage bis Beginn
- 25,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Injection site pain
Symptomtext
pt came in on 01/05 received pfizer bivalent vaccine instead of 1st monovalent pfizer vaccine. pt doesnt have any adverse reaction to the vaccine except soreness at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 26.01.2023
- Beginn
- 30.01.2023
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain in extremity
Peripheral swelling
Symptomtext
Pain and redness above middle finger on top of hand in right arm 3 days after injection. Increased redness and swelling noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 31.01.2023
- Impfdatum
- 29.10.2022
- Beginn
- 15.01.2023
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I was on a cruise ship when I started to experience symptoms of congestion in my head and aches throughout my body. I went to the doctor's office, located on the ship, and was tested for COVID-19. The test came back positive. I was not prescribed PAXLOVID on the ship. I was given FLONASE and SUDAFED D. I tested negative on 01/24/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Covid-19
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Metformin; coQ10; SINGULAIR; multivitamin; B12 (once a month)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 29.01.2023
- Impfdatum
- 28.09.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 3,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tryptase
Urticaria chronic
Symptomtext
Chronic urticaria- since daily, worsening, antihistamine resistant
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria chronic
- Hospital-Tage
- -
- Labordaten
- Trypase 15.8, 12/09/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Ramipril Simvastatin Omeprazole Wellbutrin Trazadone
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 27.01.2023
- Impfdatum
- 26.01.2023
- Beginn
- 26.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Injection site pain
Product storage error
Symptomtext
Patient dis not have any reaction to vaccine. She wa administered an expired vaccine punctured the day before and was left in the fridge.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None was done because the patient confirmed she has no adverse reaction aside from having pain in injection site.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma
- Andere Medikamente
- Allergy medication
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 05.01.2023
- Beginn
- 05.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Headache
Myalgia
Neck pain
Pain
Symptomtext
Severe left bicep pain radiates into left trapezius and cervical neck, Loss of large amout of hair on head, chronic H/A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- CKD 3A, mild HTN
- Andere Medikamente
- Lisinopril, Gabapentin, Trazadone, PremPro, D3, B12, Biotin
- Allergien
- PCN
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 23.01.2023
- Impfdatum
- 21.10.2022
- Beginn
- 04.01.2023
- Tage bis Beginn
- 75,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Insomnia
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
On the night of 01/04/2023, I started to experience some nasal drainage and had a slight fever. I had a lot of trouble sleeping that evening and when I woke up the next morning, I had a fever of 101.7. I did a home test, for Covid-19, and the test came back positive. I waited for the local clinic to open. I informed them that I tested positive and they prescribed PAXLOVID to me. I took PAXLOVID as prescribed and I feel that it helped me. My fever seemed to be gone in about 48 hours. The first day I really felt myself again though was 01/21/2023. I was sick for about two and a half weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Covid-19
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Losartan; nasal spray; CLARITIN; multivitamin; CALTRATE; vitamin B12.
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 22.01.2023
- Impfdatum
- 17.12.2022
- Beginn
- 18.12.2022
- Tage bis Beginn
- 1,0
- 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-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 20.01.2023
- Impfdatum
- 06.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Ankle fracture
Complex regional pain syndrome
Interchange of vaccine products
Limb injury
Nervous system disorder
Off label use
Product use issue
Symptomtext
ankle fracture; sympathetic nerve system issue; arm didn't go dead and this condition that developed and has him in Physical Therapy for 6 months; off label use; Product use for unapproved combination; Interchange of vaccine products; developed CRPS which is Complex Regional Pain Syndrome; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 57-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 06Dec2022 as dose 5 (booster), single (Lot number: GJ6739) at the age of 57 years intramuscular, in left arm for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), on 06Dec2022 as dose number unknown,single (Batch/Lot number: unknown) for influenza immunisation. The patient's relevant medical history included: "stomach bug", start date: Aug2022, stop date: Oct2022, notes: He had a stomach bug from August to October but went away. Concomitant medication(s) included: CILNIDIPINE, start date: Jan2023; IBUPROFEN. Vaccination history included: moderna coviD-19 vaccine (DOSE 1, SINGLE, Lot number: 030M20A, via an intramuscular), administration date: 06Feb2021, for COVID-19 immunisation; moderna coviD-19 vaccine (Dose 2, Single, Lot number: 026A21A, via an intramuscular), administration date: 06Mar2021, for COVID-19 immunisation; moderna coviD-19 vaccine (Dose 3 (Booster), Single, Lot number: 067F21A, via an intramuscular), administration date: 15Nov2021, for COVID-19 immunisation; moderna coviD-19 vaccine (Dose 4 (Booster), Single, Lot number: 6A8L21A could be a 64 instead of 6A, via an intramuscular), administration date: 30Mar2022, for COVID-19 immunisation. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 06Dec2022, outcome "unknown"; PRODUCT USE ISSUE (non-serious) with onset 06Dec2022, outcome "unknown", described as "Product use for unapproved combination"; OFF LABEL USE (non-serious) with onset 06Dec2022, outcome "unknown"; COMPLEX REGIONAL PAIN SYNDROME (non-serious) with onset Dec2022, outcome "unknown", described as "developed CRPS which is Complex Regional Pain Syndrome"; ANKLE FRACTURE (medically significant), outcome "unknown"; NERVOUS SYSTEM DISORDER (non-serious), outcome "unknown", described as "sympathetic nerve system issue"; LIMB INJURY (non-serious), outcome "unknown", described as "arm didn't go dead and this condition that developed and has him in Physical Therapy for 6 months". The event "developed crps which is complex regional pain syndrome" required physician office visit and emergency room visit. Therapeutic measures were taken as a result of limb injury. Clinical course: Would be getting another update and was 9 months and precautionary. No other conditions & investigations. Caller was not diabetic or have high cholesterol or have high blood pressure which could contribute to this. This was sympathetic nerve system issue and he was healthy. He had a stomach bug from August to October but went away. Vaccination Facility Type: Clinic. No Vaccine Administered at Facility. Caller received the Bivalent COVID-19 Vaccine with the Flu shot on the same day. Manufacturer name and lot number: unknown. He had no immediate and arm didn't go dead and this condition that developed and had him in physical therapy for 6 months. His older brother is a physician and told him he should notify Pfizer. He stated that this was what it was and would still get vaccine again. He knew there wasn't any difference in changing and he wouldn't have but this was what the facility had. Other than people being a little more tired on Pfizer, he didn't expect a reaction on Pfizer. Yes prior vaccinations (within 4 weeks) If applicable, list any other vaccinations within four weeks prior to the first administration date of the suspect vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Complex regional pain syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Gastric disorder (He had a stomach bug from August to October but went away)
- Andere Medikamente
- CILNIDIPINE; IBUPROFEN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 19.01.2023
- Impfdatum
- 16.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Symptomtext
After receiving the vaccine, I had intermittent pain but the next day it was constant. The pain is on the right side and is a radiating pain. It progresses all day long. I have been to my doctor and to a pain management doctor. I am at a point of trying to figure out what is going on.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Metformin
- Allergien
- Bee venom; chemo medication
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 18.01.2023
- Impfdatum
- 16.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Blood test
Bone pain
Headache
Symptomtext
I never had any side effects before with the covid and flu vaccinations together. I got the flu, covid, and shingrix vaccination on December 16th, 2022. The shingles shot has my bones aching terribly. I have headaches, and joint aches. I have never been diagnosed with arthritis. I made 60 November 6, and I got the shingle shot with my covid booster and my flu shot. I am calling to report the Shingle shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- blood test from doctor
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- egg whites, beta dye solution (disinfectant solution placed on you prior to surgery), other allergies.
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 16.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 07.01.2023
- Tage bis Beginn
- 10,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Headache
Pain in extremity
SARS-CoV-2 test positive
Symptomtext
I just had a sore arm for a day or two after receiving the vaccine. I had a headache off and on two days prior to testing positive for COVID-19 which is unusual for me. I tested positive on 01/07/2023 with a home test. Two days later at the clinic they tested be again and COVID-19 and it was positive, so they got a prescription for PAXLOVID. I tolerated the medication, but it left a metallic taste in my mouth. As of today, I still have fatigue and the headaches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 07JAN2023 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Sulfa
- Vorherige Impfungen
- The first two COVID-19 vaccines, my arm hurt me more than the boosters.
- Staat
- OH
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 13.01.2023
- Impfdatum
- 13.10.2022
- Beginn
- 15.12.2022
- Tage bis Beginn
- 63,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Influenza like illness
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I thought I was getting the flu. The next day I had a fever which went up to 102.7 the next day. I was able to get an appointment the next day. I was given a COVID-19 PCR test on 12/17/2022 and it was positive. I was given the standard medication and I had taken a nighttime cold and flu medication over the counter, so I was beginning to feel better. After 2 or 3 more days, I no longer had any symptoms. I have recovered from all of the symptoms. I have felt very well the last 3 weeks. I recovered very rapidly from it with no lingering effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID-19 PCR test 12/17/2022 positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Hydrochlorothiazide; lisinopril
- Allergien
- N/A
- Vorherige Impfungen
- Unknown vaccine reaction, I was sick for a day or 2 and ended up with a scar on my shoulder when I was about 5 years old.
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 13.01.2023
- Impfdatum
- 13.10.2022
- Beginn
- 25.12.2022
- Tage bis Beginn
- 73,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Hypersomnia
Influenza like illness
SARS-CoV-2 test positive
Sneezing
Upper-airway cough syndrome
Symptomtext
On 12/25/2022 I had flu-like symptoms, postnasal drip, cough, fatigue. I slept most of the day. I tested positive on 12/26/2022 and contacted my provider via telehealth and she prescribed PAXLOVID. I finished the 5-day course of medication for treatment. Also my wife and son contacted COVID-19 48 hours after my positive test. My wife and son are both negative as of now. I am still testing positive for COVID-19. I also still have a postnasal drip and sneezing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 26DEC2022 COVID-19 positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Environmental Allergies
- Andere Medikamente
- Testosterone cypionate; losartan; vitamin D; famotidine; montelukast; aspirin; PROVENTIL; cetirizine; tadalafil; TRULICITY; SYMBICORT
- Allergien
- N/A
- Vorherige Impfungen
- Allergy injection, 2018, I had to get a EpiPen injection following allergy injection.
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 30.09.2022
- Beginn
- 23.12.2022
- Tage bis Beginn
- 84,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Discomfort
Headache
Rhinorrhoea
SARS-CoV-2 test positive
Sluggishness
Symptomtext
I had a headache, sluggish, slight sniffles, and felt uncomfortable. I tested positive for COVID-19. I talked to a doctor, but he did not prescribe me anything because my symptoms were not severe.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 12/26/2022, COVID-19 test, positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Obese
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 27.09.2022
- Beginn
- 08.01.2023
- Tage bis Beginn
- 103,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chills
Ear discomfort
Fatigue
Flushing
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Sleep disorder
Swelling
Symptomtext
01/08 began having flushness in face and began having chills. Was not running fever. 01/09 Woke up in the middle of the night with a lot of congestion, pressure in my ears, swelling in my neck, and sore throat. In the morning when I woke up I took a COVID-19 test and it was positive. Called PCP and was prescribed PAXLOVID. Symptoms have maintained and I have also had extreme fatigue. Developed metallic taste in my mouth after beginning PAXLOVID. 01/11/2023 Symptoms have been improving but still very fatigued.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 test positive
- Aktuelle Erkrankungen
- Asthma had been acting up
- Vorgeschichte
- Asthma; Narcolepsy; Hypertension; hyperlipidemia; B12 deficiency
- Andere Medikamente
- Modafinil; simvastatin; aripiprazole; loratadine; furosemide; losartan; vitamin B12; calcium with vitamin D3 and potassium; SYMBICORT; albuterol as needed
- Allergien
- BACTRIM; amoxicillin; meloxicam; cat dander; mold; mildew
- Vorherige Impfungen
- First two covid-19 vaccines gave me mild flu like symptoms for 24 hours.
- Staat
- MA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 11.10.2022
- Beginn
- 31.12.2022
- Tage bis Beginn
- 81,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Headache
Malaise
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Upper-airway cough syndrome
Symptomtext
Starting 12/31/2022, I woke up with a lot of post nasal drip, congestion, headache and a slight sore throat. I tested myself with an at-home COVID-19 test and that came back negative. The symptoms got worse and the next day (01/01/2023) I tested myself again at home and it was positive. I called the doctor then, but due to it being the weekend and a holiday, they told me to hydrate and take vitamin C and vitamin D. She said to call into the office on Tuesday 01/03/2023. They called me that day and set up a telehealth visit for an hour later. I was prescribed PAXLOVID and told to stop the statins while taking the PAXLOVID. I got the lower dose of the PAXLOVID. To this day, I still have post nasal drip and a little congestion, but no headache or sore throat. I am still testing positive as of yesterday. I will test again on Thursday. The worst symptom I experienced was the sore throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- At-home COVID-19 test (12/31/2022): negative; At-home COVID-19 test (01/01/2023): positive; At-home COVID-19 test (01/08/2023): positive; At-home COVID-19 test (01/10/2023): positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Atrial Fibrillation; Thyroid Cysts; Pancreatic Cysts; 2 Knee replacements; High Blood Pressure; Low Sodium
- Andere Medikamente
- ZYRTEC; metoprolol; multivitamin; omeprazole; calcium citrate; aspirin; losartan; atorvastatin; PEPCID; vitamin D; CITRACAL; stool softener; flaxseed oil
- Allergien
- Sulfa; mold
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 06.01.2023
- Beginn
- 07.01.2023
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Cough
Fatigue
Pain
Symptomtext
I had increased symptoms of chills, body aches and fatigue with my dose 4 COVID-19 vaccine. I then on 01/09/2023 had a severe bronchial cough similar to when I had previously had COVID-19 so I called my doctor and he refilled an inhaler prescription albuterol sulfate my cough subsided but fatigue and no energy continued chills have subsided. As of the report date fatigue and lack of energy continues but gradually improving.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Hydrochlorothiazide; vitamin D; B12; fish oil; garlic; zinc; magnesium glycinate; probiotic
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 09.10.2022
- Beginn
- 04.01.2023
- Tage bis Beginn
- 87,0
- Dosis
- 1
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Diarrhoea
Dizziness
Headache
Malaise
Nasal congestion
Oropharyngeal pain
Pain
Pain in extremity
Pyrexia
SARS-CoV-2 test positive
Taste disorder
Symptomtext
After the vaccination, I had a sore arm and a slight fever. I woke up on January 4, 2023, with a sore throat and a 100-degree fever. I had a little bit of diarrhea. Certain foods tasted different. I also had aches, weakness, and a headache. I've also experienced a wave of dizziness a few times. I've also had a stuffy nose and blow my nose frequently. On January 5, 2023, I had a telehealth appointment with my doctor for a different issue. I mentioned I was sick and asked if I should test for COVID-19 at home. She said yes. I took a COVID-19 test at home. The result was positive. I sent her a message after receiving my results to get advice on how to proceed. She told me to quarantine for five days. She said to wear a mask after five days if I left the house.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 01/05/2023 at home COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arrhythmia; Atrial Fibrillation; Ulcerative Colitis; Retinal Hemorrhage
- Andere Medikamente
- Metoprolol tartrate; ELIQUIS; quazepam; vitamin D3; vitamin B complex; METAMUCIL; RESTASIS
- Allergien
- Seasonal; penicillin; sulfa drugs; nonsteroidal anti-inflammatory drugs; aspirin; ZOLOFT; CELEXA; BENTYL; KEFLEX
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 21.12.2022
- Tage bis Beginn
- 72,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
COVID-19
Chills
Cough
Fatigue
Headache
Oropharyngeal pain
Pain
Parosmia
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I started having fever and sore throat I did a home test, and I was negative and then I went to a pharmacy and did a PCR test that was positive for COVID-19. I had a virtual consult with my doctor and was given PAXLOVID, azelastine hydrochloride nasal spray, TESSALON PERLES and albuterol. Within a few days of the results I started having headache, runny nose, congestion, body aches, chills, coughing, loss of smell and fatigue. These symptoms lasted for two weeks in total. Although I am still having cough, fatigue and my sines of smell is off (smelling smoke for some reason).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- COVID-19 test, PCR test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; History of Migraines; Ulcers
- Andere Medikamente
- CLARITIN
- Allergien
- N/A
- Vorherige Impfungen
- Flu shot, swelled up
- Staat
- NJ
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 09.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 86,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Middle insomnia
Oropharyngeal pain
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
Positive Covid test after vaccination. Woke up congested and sore throat in middle of the night. Headache and body ache continues with congestion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Home Covid test positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Arthritis; haploidic migraines; spin stenosis; bipolar; idiopathic intracranial hypertension
- Andere Medikamente
- Gabapentin; coq10; NEXIUM; ADDERALL; LAMICTAL; QSYMIA; MOBIC; melatonin; KLONOPIN; CYMBALTA; LOVAZA; LIPITOR; RISPERDAL; methylated folate; spironolactone; probiotic; vitamin D; biotin; vitamin B complex; vitamin C; CENTRUM; calcium; butter
- Allergien
- Medications
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 09.01.2023
- Impfdatum
- 20.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Amenorrhoea
Fatigue
Pregnancy test negative
Symptomtext
Menstrual cycle ceased . None since administration of bivalent (2 cycles) , negative pregnancy test. Fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Pending
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Adderall, viibryd, spirolactone
- Allergien
- Keflex
- Vorherige Impfungen
- Pfizer booster 3- cardiac issues
- Staat
- PA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 07.01.2023
- Impfdatum
- 20.12.2022
- Beginn
- 25.12.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Computerised tomogram head
Discomfort
Dizziness
Dyspepsia
Full blood count
Headache
Nausea
Urine analysis
Visual impairment
Symptomtext
Gradual onset of headache, pressure, dizziness, visual disturbances, nausea, indigestion which have become constant and still exist. Visited the E.R. at the hospital on December 31, 2022. Was treated with Benadryl, Ativan, Toradol to break headache. Sent home. Symptoms still persist. Visited neurologist January 6, 2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Head CT, CBC, Urinalysis. December 31, 2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Migraine
- Andere Medikamente
- Xyzal, Maxalt, Ativan
- Allergien
- Anastrazole, Seasonal Allergies, Apples, Trees
- Vorherige Impfungen
- Similar dizziness and headache with prior Pfizer booster, but was unaware that the vaccine had caused the issue. It lasted 5 mon
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 10.12.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 19,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Hypomenorrhoea
Menstruation irregular
Symptomtext
About 19 days after taking the vaccine, I had a menstrual period at the age of 69. This period was just like the ones I had when I was young except a bit lighter and lasted about six days, then stopped. I had no other symptoms and now I'm fine. I have no other explanation for this except for the vaccine, after which I was very tired for several days. I also had COVID 19 in late Sept/October for which I was treated with Paxlovid, which helped tremendously. I feel certain that the period was caused by the vaccine and the illness. I am a retired RN with 43 years of experience.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None. I have a routine visit with my PCP scheduled in February.
- Aktuelle Erkrankungen
- Had COVID 19 in late September of 2022 and through month of October.
- Vorgeschichte
- Asthma
- Andere Medikamente
- Pulmicort Flexhaler, Serevent Diskus, Thyroid NP 30 mg/day, bioidentical estrogen-progesterone troches, Montelukast 10 mg/day, Rootology herbal allergy caps
- Allergien
- Allergic to Flagyl
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 06.01.2023
- Impfdatum
- 04.10.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 69,0
- Dosis
- 5
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I tested positive forCOVID-19 on Tuesday December thirteen. My Doctor prescribed medication the same day. I was tired and had fever the first couplie of days. I do not think I had a fever by the fifth day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 positive test.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma
- Andere Medikamente
- Levothyroxine; Liothyronine; Perezone; Montelukast; Vitamin D; Vitamin B12
- Allergien
- Penicillin; Tomato
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 05.01.2023
- Impfdatum
- 05.10.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 49,0
- Dosis
- 5
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Joint lock
Magnetic resonance imaging spinal abnormal
Pain
X-ray limb abnormal
Symptomtext
On December 13, 2022, I woke up and my knees were locked, and it was painful. I had to slowly unfurl my knees, especially my right one. I visited my doctor on November 23, 2022. I had an X-Ray. The pains began to spread to other parts of my body. I visited my orthopedist on December 8th. I had an MRI for my lumbar back. But the pains were now in my lower back, right hip, and shoulders. The pain is sharp to dull ache, especially when I move. I am using topical ointments to help relieve the pain. I have a follow-up appointment with my orthopedist on January 19, 2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- X-Ray, abnormal, 11/23/2022; MRI, abnormal, 012023
- Aktuelle Erkrankungen
- Urinary Tract Infection
- Vorgeschichte
- Gastroparesis; Hepatitis; Interstitial Cystitis; Uveitis; Glaucoma; Type 2 Diabetes; Herpes Symplex 2; Diverticulitis; Thyroiditis; Osteo Arthritis;
- Andere Medikamente
- Losartan; vitamin D3; montelukast; levocetirizine; metformin; albuterol; megastore; menaquinone K2-7; omega acid; SE ZYME FORTE; zinc; rosuvastatin; fish oil; vitamin C; LEVOXYL; vitamin B12; MOTILIUM
- Allergien
- LEVAQUIN; CTE found in hair dye; sensitivity to gluten; grains; nuts; grass; trees.
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 05.01.2023
- Impfdatum
- 21.12.2022
- Beginn
- 04.01.2023
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dry throat
Neck pain
Oropharyngeal pain
Pain
Pain in jaw
SARS-CoV-2 test negative
Streptococcus test negative
Tonsillitis
Symptomtext
Around 07:15AM ET on 0/04/2023 I woke up with a dry throat and made tea to help but my throat become so sore I went to urgent care around 2PM ET that afternoon it felt like needle in my throat and my neck under my jaw began to hurt and it was throbbing . I had no fatigue or other symptoms just the pain. At Urgent Care a Strep and COVID-19 tests were performed both tests were negative. At an inspection of my throat I was diagnosed with tonsillitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- Strep and COVID-19 both were negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 05.01.2023
- Impfdatum
- 03.10.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 29,0
- Dosis
- 6
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Influenza virus test negative
Malaise
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test negative
Upper-airway cough syndrome
Symptomtext
I had post nasal drip, clogged head, cough, chest congestion, feeling horrible all over, sore throat. I was prescribed 4 days z-pack. I get this every fall.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COID-19, Flu test - negative
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Multiple Sirois; Rheumatoid arthritis; Autoimmune diseases 12 total
- Andere Medikamente
- Hydroxyquinone; Tylenol; Aspirin; Amlodipine; Hydrochlorothiazide; Atorvastatin; Duloxetine; Tramadol; Biotin
- Allergien
- Sulfur; Morphine
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 01.01.2023
- Impfdatum
- 28.12.2022
- Beginn
- 30.12.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Diarrhoea
Fatigue
Pyrexia
Symptomtext
Fever, Diarrhea, exhaustion
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Hypereosinophilia hypertension Long Covid Syndrome
- Vorgeschichte
- Hypothyroidism Menopause Otosclerotic hearing impairment
- Andere Medikamente
- estradiol 1 mg qd progesterone 5 mg qd synthroid 100 mcg qd lisinopril 20 mg bid Carvedilol 12.5 mg bid KCl 10 mEq bid Magnesium 250 mg bid klonopin 0.5 mg PRN hs multivitamin qd vit c qd vit b12 qd vit b complex qd calcium 1000 mg qd vit
- Allergien
- Antihistamines
- Vorherige Impfungen
- Pfizer Covid vaccine #2 @ age 67 flu-like symptoms with severe persistent myalgia 02\04\2021
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 31.12.2022
- Impfdatum
- 06.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site mass
Injection site pain
Symptomtext
Redness, pain at injection site, a lump at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Tetanus , other covid vaccines
- Staat
- MN
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 30.12.2022
- Impfdatum
- 19.12.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Body temperature
Dizziness
Malaise
Myalgia
Pyrexia
Vaccination site pain
Symptomtext
dizzy; weak; feeling terrible; at injection site hurts/injection site pain is in her right upper arm; muscle pain; fever; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 74-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 19Dec2022 as dose 5 (booster), single (Lot number: GJ6739) at the age of 74 years, in right arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: PRAVASTATIN. Vaccination history included: BNT162b2 (1st dose Pfizer COVID-19 Vaccine:, Date Received: 26Jan2021, Lot number: unknown, Route of Administration: Intramuscular), administration date: 26Jan2021, when the patient was 72-year-old, for Covid-19 immunization; BNT162b2 (2nd dose Pfizer COVID-19 Vaccine:, Date Received: 17Feb2021, Lot number: EN6201, Route of Administration: Intramuscular), administration date: 17Feb2021, when the patient was 72-year-old, for Covid-19 immunization; BNT162b2 (3rd dose Pfizer COVID-19 Vaccine:, Date Received: 13Oct2021, Lot number: 30155ISA, Route of Administration: Intramuscular), administration date: 13Oct2021, when the patient was 73-year-old, for Covid-19 immunization; BNT162b2 (4th dose Pfizer COVID-19 Vaccine:, Date Received: 22Apr2022, Lot number: FM9992, Route of Administration: Intramuscular), administration date: 22Apr2022, when the patient was 73-year-old, for Covid-19 immunization. The following information was reported: VACCINATION SITE PAIN (non-serious) with onset 20Dec2022, outcome "not recovered", described as "at injection site hurts/injection site pain is in her right upper arm"; DIZZINESS (non-serious) with onset 20Dec2022, outcome "not recovered", described as "dizzy"; MALAISE (non-serious) with onset 20Dec2022, outcome "not recovered", described as "feeling terrible"; PYREXIA (non-serious) with onset 20Dec2022, outcome "not recovered", described as "fever"; MYALGIA (non-serious) with onset 20Dec2022, outcome "not recovered", described as "muscle pain"; ASTHENIA (non-serious) with onset 20Dec2022, outcome "not recovered", described as "weak". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: Other conditions was noted as no. Vaccination facility type was noted as clinic. Patient was calling about third Booster Bivalent COVID-19 Vaccine. She had the booster yesterday (19Dec2022) and today (20Dec2022) when she woke up, she was feeling terrible and have not had that reaction to her previous Pfizer vaccines. She was dizzy, weak, at injection site hurts, muscle pain, and fever. These started on 20Dec2022 (today) when she woke up. These symptoms were still ongoing and were about the same. Patient clarified the injection site pain is in her right upper arm. Adverse events require visit to emergency room and physician's office were noted as no. Investigations was noted as no.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221220; Test Name: Fever; Result Unstructured Data: Test Result:Unknown results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
- Andere Medikamente
- PRAVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 28.12.2022
- Impfdatum
- 27.09.2022
- Beginn
- 24.12.2022
- Tage bis Beginn
- 88,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest discomfort
Cough
Diarrhoea
Headache
Influenza virus test positive
Insomnia
Lymphadenopathy
Nasal congestion
Nausea
Oropharyngeal pain
Respiratory tract congestion
Restlessness
SARS-CoV-2 test positive
Vomiting
Symptomtext
Extreme headache, nausea, vomiting, diarrhea, sore throat, swollen glands, coughing, a lot of congestion and blowing of the nose, chest congestion and pressure restlessness or sleeplessness. No fever but had an extreme metal taste in mouth once started on PAXLOVID also experienced extreme loss of appetite.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Flu test, Covid test came back positive, received PAXLOVID
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Arthritis; Two complete spinal reconstruction
- Andere Medikamente
- Lisinopril HCTZ; probiotic; fish oil
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 28.12.2022
- Impfdatum
- 26.09.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 70,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Nephrolithiasis
Pain
Vomiting
Symptomtext
3mm kidney stone Treatment for pain and vomiting Passed on its own Normal outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity
- Andere Medikamente
- Immitrex as needed for migraine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 24.12.2022
- Impfdatum
- 17.12.2022
- Beginn
- 18.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Pain
Pyrexia
Symptomtext
Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Medium, Systemic: Headache-Medium, Additional Details: pt states silver dollar sized red, swollen, hot, a little itchy spot where vaccine was given, also felt headache, aches, fever, taking advil, wants to see dr just to make sure nothing else going on, told her she needs to do what makes her most comfortable
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 11.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site bruising
Symptomtext
Site: Bruising at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 54,0
- Geschlecht
- U
- Eingang
- 22.12.2022
- Impfdatum
- 29.11.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
COVID-19
Drug ineffective
Feeling abnormal
Full blood count
Glycosylated haemoglobin
Hepatic enzyme abnormal
Interchange of vaccine products
Investigation
Metabolic function test
Pain in extremity
Pyrexia
SARS-CoV-2 test
Thyroid function test
Symptomtext
interchange of vaccine product; felt so bad, it was negative but first they come positive; felt so bad, it was negative but first they come positive; I have not felt good since I got it; I felt so bad; my toes hurt, they just ache all the time, it's extremely painful; I am waking up at odd hours at night with toe pain; Fever; 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 54-year-old patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 29Nov2022 as dose number unknown (booster), single (Lot number: GJ6739) at the age of 54 years for covid-19 immunization; elasomeran (MODERNA COVID-19 VACCINE), as dose number unknown, single (Batch/Lot number: unknown) for covid-19 immunization. The patient's relevant medical history included: "have type 1 diabetes" (unspecified if ongoing), notes: Yes, I have type 1 diabetes (Captured as provided) and heart disease; "heart disease" (unspecified if ongoing), notes: Yes, I have type 1 diabetes (Captured as provided) and heart disease. The patient took concomitant medications. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant), outcome "unknown", described as "interchange of vaccine product "; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "felt so bad, it was negative but first they come positive"; FEELING ABNORMAL (non-serious), outcome "unknown", described as "I have not felt good since I got it; I felt so bad"; PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "my toes hurt, they just ache all the time, it's extremely painful; I am waking up at odd hours at night with toe pain"; PYREXIA (non-serious), outcome "unknown", described as "Fever". The patient underwent the following laboratory tests and procedures: Blood test: (29Nov2022) the lab test was all normal, notes: I have blood test the same day I had the vaccine and the lab test was all normal; Full blood count: (unspecified date) all that's normal; Glycosylated haemoglobin: (unspecified date) all that's normal; Hepatic enzyme abnormal: (unspecified date) all that's normal; Lab work: Consumer stated, "Yes, I have and its all normal: (unspecified date) all normal, notes: Lab work: Consumer stated, "Yes, I have and its all normal; Metabolic function test: (unspecified date) all that's normal; SARS-CoV-2 test: (unspecified date) Negative, notes: felt so bad, it was negative but first they come positive; (unspecified date) Positive; Thyroid function test: (unspecified date) all that's normal. Therapeutic measures were taken as a result of pain in extremity. Clinical information: Consumer stated, I have the vaccine on 29Nov (Received Pfizer COVID-19 Bivalent vaccine), prior to that I had have the Moderna vaccine(COVID-19 vaccine)but they told me I could go ahead and have the Pfizer Bivalent(suspect captured as Pfizer COVID-19 Bivalent vaccine) because my pharmacy was out of the Moderna. Consumer stated, Yeah, I had the Moderna. I already got it on 29Nov, and I will be honest with you I have not felt good since I got it. I went and got a Covid test. I felt so bad, it was negative but first they come positive then they said oh no we did wrong one we did the Covid vaccine and you have it before it. What bothers me the most is my toes hurt, they just ache all the time, it's extremely painful and then I get fever on occasion. I mean I don't know it's because this. Height and Weight: Consumer stated, "I am 5'6 and weigh probably about 154 or so. Consumer stated, "Yes, I have and it's all normal. I have blood test the same day I had the vaccine, and the lab test was all normal. I had everything done my A1C, liver enzyme, thyroid panel, CMP, CBC all that's normal but that was before I got the shot, right before I got it. Treatment: Consumer stated, "Like its 4 O' clock in the morning and this toe pain, it was horrible. I just took Tylenol. I do take blood thinners, I don't know you if you need to know that because I have the heart disease.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221129; Test Name: blood test; Result Unstructured Data: Test Result:the lab test was all normal; Comments: I have blood test the same day I had the vaccine and the lab test was all normal; Test Name: CBC; Result Unstructured Data: Test Result:all that's normal; Test Name: A1C; Result Unstructured Data: Test Result:all that's normal; Test Name: liver enzyme; Result Unstructured Data: Test Result:all that's normal; Test Name: Lab work: Consumer stated, "Yes, I have and its all normal; Result Unstructured Data: Test Result:all normal; Comments: Lab work: Consumer stated, "Yes, I have and its all normal; Test Name: CMP; Result Unstructured Data: Test Result:all that's normal; Test Name: felt so bad, it was negative but first they come positive; Test Result: Negative ; Comments: felt so bad, it was negative but first they come positive; Test Name: felt so bad, it was negative but first they come positive; Test Result: Positive ; Test Name: thyroid panel; Result Unstructured Data: Test Result:all that's normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Heart disease, unspecified (Yes, I have type 1 diabetes (Captured as provided) and heart disease); Type 1 diabetes mellitus (Yes, I have type 1 diabetes (Captured as provided) and heart disease)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 17.12.2022
- Beginn
- 17.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Pain
Pain in extremity
Symptomtext
Third Shot (Booster): Manufacturer: Moderna; my whole body kind of ached a little bit; arm starting to feel very sore; 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 female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 17Dec2022 at 15:00 as dose 4 (booster), single (Lot number: GJ6739) at the age of 39 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Exercise induced asthma" (unspecified if ongoing), notes: Exercise induced asthma; "HLA-B27 associated anterior uveitis" (unspecified if ongoing), notes: which is an autoimmune disease of my eye. Concomitant medication(s) included: FISH OIL; VITAMIN D3. Vaccination history included: BNT162b2 (DOSE 1, SINGLE, LOT#EL3247), administration date: 23Feb2021, when the patient was 37-year-old, for COVID-19 immunization; BNT162b2 (DOSE 2, SINGLE, LOT# EL3247), administration date: 16Mar2021, when the patient was 37-year-old, for COVID-19 immunization; moderna (DOSE 3 (BOOSTER), SINGLE,), administration date: 01Dec2021, when the patient was 38-year-old, for COVID-19 immunization; Flu shot, administration date: Sep2022, when the patient was 39 years old, for Immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 17Dec2022, outcome "unknown", described as "arm starting to feel very sore"; PAIN (non-serious) with onset 17Dec2022, outcome "unknown", described as "my whole-body kind of ached a little bit"; INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 17Dec2022 at 15:00, outcome "unknown", described as "Third Shot (Booster): Manufacturer: Moderna". Therapeutic measures were not taken as a result of pain, pain in extremity. Additional information: When the needle goes in, it hurts a little bit; 8 hours later, my arm starting to feel very sore. Consumer stated, "So for myself, so actually, we got our shots yesterday, at about 3 pm. I, you know, other than, obviously, you know, when the needle goes in, you know, it hurts a little bit. But other than that, I was fine until about probably 11 or so. So, about 8 hours later, and then, my arm starting to feel very sore and then overnight as I was sleeping, my arm would have gotten worse in terms of soreness and the, my whole-body kind of ached a little bit, you know, up to the point where it woke me up earlier then I had been planning to wake up. And instead of, all day today it was just the same thing, general overall soreness but most specifically in the arm, I received my shot, which was my left arm." Moderna: Reason for no lot number: of Covid Vaccine: Other: LOT#: Consumer stated, "I hope that I could read the handwriting. Looks like 045J21A, I think. This J could also be something else, but I think it's J." Flu Shot: Reason for no lot number: of Unspecified Flu Shot: Other: LOT# could not be probed as the shot was unspecified. Lab Work reported as no. Treatment reported as no. concomitant medication: birth control pill, multivitamin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anterior uveitis (which is an autoimmune disease of my eye.); Exercise induced asthma
- Andere Medikamente
- FISH OIL; VITAMIN D3
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 22.12.2022
- Impfdatum
- 14.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling hot
Glycosylated haemoglobin
Pain in extremity
Peripheral swelling
Rash
Symptomtext
I had a little red rash and along in my arm; a little swollen and it hurts; a little red rash and along in my arm and heat; a little swollen and it hurts; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 68-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 14Dec2022 as dose number unknown (booster), single (Lot number: GJ6739) at the age of 68 years for covid-19 immunisation. The patient's relevant medical history included: "Blood pressure high" (unspecified if ongoing), notes: Blood pressure high; "High cholesterol" (unspecified if ongoing), notes: High cholesterol; "GERD" (unspecified if ongoing), notes: GERD; "Type 2 diabetic" (unspecified if ongoing), notes: Type 2 diabetic; "vision problems" (unspecified if ongoing), notes: Avastin shots for in my right eye; "little mini stroke", start date: Dec2013 (unspecified if ongoing). Concomitant medication(s) included: METFORMIN ER oral; OZEMPIC taken for diabetes mellitus; GLIPIZIDE; LIVALO taken for blood cholesterol abnormal; EZETIMIBE oral; BABY ASPIRIN; VITAMIN D 2000; PEPCID [FAMOTIDINE] taken for gastrooesophageal reflux disease. Vaccination history included: Covid-19 vaccine (Primary immunization series completed, Unknown manufacturer), for Covid-19 immunization. The following information was reported: RASH (non-serious) with onset Dec2022, outcome "not recovered", described as "I had a little red rash and along in my arm"; FEELING HOT (non-serious) with onset Dec2022, outcome "not recovered", described as "a little red rash and along in my arm and heat"; PAIN IN EXTREMITY (non-serious), PERIPHERAL SWELLING (non-serious) all with onset Dec2022, outcome "not recovered" and all described as "a little swollen and it hurts". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of rash, pain in extremity, feeling hot, peripheral swelling. Additional Information: Treatment: Consumer stated that When she first got home I took Tylenol and she put ice pack on it for the first 2 days, and then the last 2 days, she have aloe Vera cream in my refrigerator and she have been putting refrigerated aloe Vera cream on it and it seems to help. Consumer stated that Monday I had my A1C check and it was 7.5." (Further the result was not clarified hence, not captured in tab)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Test Name: A1C test; Result Unstructured Data: Test Result:7.5
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high; GERD; High cholesterol; Stroke; Type 2 diabetes mellitus (Type 2 diabetic); Vision abnormal (Avastin shots for in my right eye)
- Andere Medikamente
- METFORMIN ER; OZEMPIC; GLIPIZIDE; LIVALO; EZETIMIBE; BABY ASPIRIN; VITAMIN D 2000; PEPCID [FAMOTIDINE]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Insomnia
Limb discomfort
Pyrexia
Urinary incontinence
Symptomtext
She got her vaccine, was feeling drooping starting that afternoon. She did not sleep that night at all, had a headache all through the night. She had a fever through the night, chills all night, her arm hurt to the degree that she was not able to do anything with it, she had to sleep flat on her back which she cannot sleep that way. She had urinary incontinence which she does not suffer from. When she went to the bathroom she almost fainted and had to sit down on the top and wait until she felt like she was not going to fall. She is not prone to any conditions of dizziness or anything. She got back to the bed. In the morning I was looking at her neck in the mirror and she had a swelling on the left side of her neck, above where the shot was from the base of the neck/collarbone, a soft tender swelling. The symptoms started easing, she had the headache through the day, was able to sleep some that evening, still had the chills. She was still having the urinary problem, and then was easing during the day. She still has a sore arm and the swelling on the neck which is less. She had a similar reaction with the third vaccine and left her a message for her. The cancer center on the phone said it may have been due to the lymphoma that she has, but when they saw her they did not feel it had anything to do with that. The headache went away by the third day. There was a doctor there when she had this vaccine, and told them about some of the problems she had in December of 2021 and they had her talk to the doctor and describe all of her symptoms, and he suggested that as soon as she get home to take 2 Ibuprofen which she did. 12/16/21 she had the vaccine and had the swelling on the neck and ended up calling the nurse on the weekend and she wanted her to go to the ER and she dealt with the doctor the following week. She saw her and she looked at it all and did not feel like it was anything serious. She has had a reaction of some kind with every vaccine, but not as severe as the third one and the swelling with the 3rd one and this one (5th vaccine).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure, lymphoma, back pain.
- Andere Medikamente
- Losartan/potassium 25 mg, Propranolol 10 mg, Celecoxid 200 mg, Fluoxetine HCL 10 mg. Evening: Nifedipine ER 60 mg.
- Allergien
- None.
- Vorherige Impfungen
- 3rd vaccine as described in description.
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 18.12.2022
- Impfdatum
- 12.12.2022
- Beginn
- 12.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Eye swelling
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Loss of personal independence in daily activities
Mouth swelling
Pruritus
Skin discolouration
Swelling face
Swollen tongue
Symptomtext
Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Allergic: Itch Generalized-Medium, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Medium, Additional Details: Tongue swollen. Arm itch, red/light purple ring, swollen & painful cannot but even shirt over it. Instructed to take benadryl, ice, see doctor or ER if worsens.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 16.12.2022
- Impfdatum
- 08.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Investigation
Pruritus
Rash
Symptomtext
Diarrhea; a rash on my left arm and shoulder; itchiness; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 78-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 08Dec2022 as dose 5 (booster), single (Lot number: GJ6739) at the age of 78 years for covid-19 immunisation. The patient's relevant medical history included: "Diabetic" (unspecified if ongoing), notes: Diabetic; "Blood pressure high" (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; Covid-19 vaccine (Dose 4, unknown manufacturer), for COVID-19 immunization. The following information was reported: DIARRHOEA (non-serious) with onset Dec2022, outcome "unknown", described as "Diarrhea"; RASH (non-serious) with onset Dec2022, outcome "unknown", described as "a rash on my left arm and shoulder"; PRURITUS (non-serious) with onset Dec2022, outcome "unknown", described as "itchiness". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were not taken as a result of diarrhoea, rash, pruritus. Additional information: Case narrative including clinical course, therapeutic measures, outcome and additional relevant information. The report not related to a study or programme. Other Conditions was yes. Investigations were reported as yes. Reason for no lot number of COVID-19 Bivalent Vaccine: Other: Consumer stated, reporter think the LOT# is GJ6739. Expiry Date of COVID-19 Bivalent Vaccine was unknown.Reporter received patient fifth Pfizer shot (later clarified ad Pfizer COVID-19 Bivalent Vaccine) at the, Thursday, 08Dec2022 and patient had a reaction. Patient believe it is a reaction and diarrhea, a rash on my left arm and shoulder, itchiness. What can patient do, what can patient take to alleviate this. Consumer was informed about the role of Pfizer Drug Safety and also informed that Pfizer Medical Information is the right department to answer the question. In response to file a safety report, Consumer stated as yes, go ahead. Reporter stated, patient think the LOT# is GJ6739. It is the Pfizer Bivalent (clarified) and it was 08Dec2022. It is the fifth shot. Any prior vaccinations (within 4 weeks) was reporter stated was no. Other medical conditions and Concomitant medications: Consumer stated, Patient was a diabetic. Patient have high blood pressure and sugar diabetes. Treatment for the medical conditions consumer stated was yes. Name of the medications patient stated was no, not at this time. Reporter stated was yes, Thursday patient had blood drawn at the. Results of the test: Consumer stated, patient don't have the results. It went straight to the doctor. Treatment in response to adverse event was no. Reassurance was stated, not at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221208; Test Name: blood drawn; Result Unstructured Data: Test Result:Unknown results; Comments: I don't have the results
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high; Diabetic
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 15.12.2022
- Impfdatum
- 09.12.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye swelling
Mouth swelling
Pruritus
Pyrexia
Swelling face
Swollen tongue
Symptomtext
Systemic: Allergic: Itch Generalized-Medium, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Medium, Systemic: Fever-Medium, Additional Details: Started with Swelling in face-then itchy neck-now itch neck, shoulders and back-continued swelling in lower lip. Fever 100.4 (12/10/2022)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 26.11.2022
- Beginn
- 27.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Impaired work ability
Muscle spasms
Pain
Pain in extremity
Symptomtext
SEVERE chronic leg pain initiating in both legs with unbearable cramping pain in thighs. Spreading down in legs. Eventually dissipating from right leg but lingering in left leg. Initially hard to even walk down the stairs, had to stop and rest. Up all night in pain. Difficulty working from pain--heat, ice, aspirin do not alleviate the pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 30.11.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Pain
Rash
Rash macular
Symptomtext
12-01-2022 (day after) woke up with red splotches on arms and legs 12-02-2022 woke up with large painful blisters around both ankles, called pharmacy and told flu shot was probably the cause 12-03-2022 went to hospital Emergency, was given steroid shot and prescription, also Mupirocin ointment 12-05-2022 blisters were extremely painful, went to family practice doctor, received antibiotic shot 12-06-2022 to current, blisters continue to be painful and are treated with ointment
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Type 2 Diabetic, Lumpectomy June 2020
- Andere Medikamente
- Metformin, Atorvastatin, Anastrozole, Lisinopril, Latanoprost, vitamin D
- Allergien
- Seasonal
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 28.10.2022
- Beginn
- 03.12.2022
- Tage bis Beginn
- 36,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anaemia
Gastrointestinal haemorrhage
Pain in extremity
Symptomtext
After receiving the vaccine, I had a sore arm for a day. On 12/03/2022 I went to the emergency room for a gastrointestinal bleed. I had no prior pain or symptoms. I was in the hospital for six days. As of today, I continue to be anemic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- 6,0
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 10.12.2022
- Impfdatum
- 09.12.2022
- Beginn
- 10.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Hyperhidrosis
Myalgia
Nausea
Pain
Pain in extremity
Pain of skin
Symptomtext
The adverse effect started at around 11pm on the 9th with my arm getting sore, body getting sore, and starting to get a headache. When I woke up at 8am, my head was hurting at an 8 pain level, my skin hurt everytime something touched it, muscles are sore when I move, I get chills even though I'm sweating, and I feel nauseous constantly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Anemia, Hypoglycemia, Chronic Migraines
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 07.12.2022
- Impfdatum
- 01.12.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Myalgia
Pyrexia
Symptomtext
Myalgia, Fever, soreness at injection site Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 06.12.2022
- Impfdatum
- 05.12.2022
- Beginn
- 07.12.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Body temperature increased
Pain
Symptomtext
High temperature , aches and pains.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- High blood pressure, heart valves
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Almodipine besylate 10 m tab
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 06.12.2022
- Impfdatum
- 05.12.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Injection site pain
Nausea
Neck pain
Pain
Pain in extremity
Sleep disorder
Spinal pain
Symptomtext
Immediate pain/burning at injection site which radiated to neck, became nauseous within 3 minutes. Ice pack was applied which helped. The patient did not want the doctor to be contacted. It was recommended that if she still had pain to follow up with her healthcare provider. The next morning, patient reported being unable to sleep last night and pain radiated to back/spine and down left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Patient stated the first two COVID-19 vaccines made her sick.
- Staat
- OH
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 06.12.2022
- Impfdatum
- 23.11.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Iridocyclitis
Pain
Weight
Symptomtext
Nongranulomatous anterior uveitis in the eye; Painful to move her eye or head; 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 75-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 23Nov2022 as dose 4 (booster), single (Lot number: GJ6739) at the age of 75 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Blood thinner" (unspecified if ongoing); "Hypothyroidism" (unspecified if ongoing), notes: Since she was a child and has been on since 18 years old. The patient's weight reported as 107 - 108 lbs. Concomitant medication(s) included: INFLUENZA VACCINE taken for immunisation as dose number unknown, single; ELIQUIS taken for anticoagulant therapy; LEVOTHYROXINE taken for hypothyroidism. Vaccination history included: moderna (DOSE 1, Lot number: 038K20A or 038K26A), administration date: 21Jan2021, for Covid-19 immunization, reaction(s): "Hives"; moderna (DOSE 2, Lot number: 006M20A), administration date: 18Feb2021, for Covid-19 immunization, reaction(s): "Hives"; BNT162b2 (DOSE 3 (BOOSTER), Route of Administration: Intramuscular, Lot number: FJ1611), administration date: 16Dec2021, for Covid-19 immunization, reaction(s): "Hives", "Interchange of vaccine products". Within 3-4 days after COVID-19 Vaccine Bivalent, patient's eye got very red, white part got swollen, and was painful to move her eye or head. She could not see well. Because this happened during a holiday, she could not see her doctor till Monday. Her doctor said she developed non-granulomatous anterior uveitis in the eye. Her doctor prescribed her eye drops and steroids which helped with pain. She knows some people have gotten this shot and have gotten this reaction and her fear is that she will lose vision in her eye. She would like to know what the outcome of people has been who have had this side effect from this shot. She wishes she had not gotten the shot. The events were assessed as serious (medically significant). The outcome of the events was unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Test Name: Weight; Result Unstructured Data: Test Result:107-108 lbs
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anticoagulant therapy; Hypothyroidism (Since she was a child and has been on since 18 years old)
- Andere Medikamente
- INFLUENZA VACCINE; ELIQUIS; LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 7,0
- Geschlecht
- M
- Eingang
- 05.12.2022
- Impfdatum
- 02.12.2022
- Beginn
- 02.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Symptomtext
Per father patient experienced a sore arm. Father reports that he did not administer tylenol or ibuprofen and did not encourage fluids per instructions from nurse at time error occurred.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- per father N/A
- Aktuelle Erkrankungen
- Father reports patient had a "cold" within the last month
- Vorgeschichte
- per father N/A
- Andere Medikamente
- Per father N/A
- Allergien
- per father N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- 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: ja
Immediate post-injection reaction
Injection site hypoaesthesia
Injection site pain
Neck pain
Pain
Symptomtext
Systemic: Pain that radiated up the neck of the patient from the injection site, followed by numbness of the arm under the injection site, both of which completely resolved within minutes of injection.-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 01.12.2022
- Impfdatum
- 29.11.2022
- Beginn
- 29.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Diarrhoea
Dizziness
Hyperhidrosis
Loss of personal independence in daily activities
Nausea
Vomiting
Symptomtext
After waiting 15 minute observation, client left the facility and was transported by van to her facility. During the van ride, she started feeling sweaty, weak, and felt faint for about 5 minutes. She turned to administrator and said "I'm going to be sick". The van stopped and she vomited, it was" chunky" (she said it was her breakfast coming up). She declined 911/EMS, she got back in the van and "felt better". As she entered the facility, she also had an episode of diarrhea. The medical office came up to assess her, vitals were normal for her (bp 90/60) taken and she rested for the remainder of the day with no other instances of nausea/vomiting or diarrhea. Rested for the next day and did not participate in groups the next day. States today, Thursday, December 1, 2022, she feels fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 11/29/2022 BP 90/60
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- depression, alcohol use
- Andere Medikamente
- Naltrexone 50mg Celexa 10 mg Gabapentin 300mg
- Allergien
- Pain medicine: Opiods
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 01.12.2022
- Impfdatum
- 29.11.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Feeling hot
Pruritus
Swelling
Symptomtext
The area is red, itchy, warm and swollen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Yeast, dairy, egg
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 25.11.2022
- Beginn
- 25.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Rash
Swelling face
Symptomtext
Pt received the Pfizer covid19 booster injection on 11/25/2022. Pt arrived to 11/28/2022 with swelling of the face and a rash on her face, ears, arms, legs, and abdomen. Dr. was contacted and ordered 50mg of Benadryl. A prescription for Medrol Dose Pack was also prescribed. To note, patient also received IV contrast for a fistulagram the same day they received the vaccine. As of 11/30 patient still has rash. On PO Medrol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CHF, ESRD
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 30.11.2022
- Impfdatum
- 29.11.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Contusion
Erythema
Nausea
Skin indentation
Skin warm
Symptomtext
The patient's mother called and said that the patient's arm was bruised, there was an indentation, it was hot and red, and that the patient also experienced nausea and chills
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 28.11.2022
- Impfdatum
- 26.11.2022
- Beginn
- 26.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Limb discomfort
Malaise
Ocular hyperaemia
Peripheral swelling
Pharyngeal swelling
Symptomtext
At around 1310 patient patient verbalized that she feels her throat is swollen. noted redness around both eyes. b/p 159/81, pulse rate 105/min. Benadryl 50mg ivp given. O2 administered at 2lpm/NC. At 1330 after treatment, patient still not feeling well, c/o feeling that her leg is swollen and heavy. epinephrine 0.3mg given IM. b/p 177/77, pulse rate 106/min. Dr, on call nephrologist notified. Called 911. Report given to paramedics. patient's daughter notified. Patient sent to ER accompanied by paramedics and patient's husband.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Anemia, DM Type 2, Hypertension, CKD, Hyperlipedemia
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 25.11.2022
- Impfdatum
- 19.11.2022
- Beginn
- 20.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
I developed hives all over my body. I was taking a steroid dose pack for my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyrodism
- Andere Medikamente
- Birth control; ARMOUR
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 22.11.2022
- Impfdatum
- 21.11.2022
- Beginn
- 22.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain
Pyrexia
Symptomtext
body aches and fever
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- pfizer en5318
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 22.11.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Pruritus
Rash erythematous
Rash pustular
Rash vesicular
Rash
SARS-CoV-2 test
Symptomtext
Red Rashy Blistery Bumps, Itchy with Pus; Red Rashy Blistery Bumps, Itchy with Pus; Red Rashy Blistery Bumps, Itchy with Pus; Red Rashy Blistery Bumps, Itchy with Pus; Interchange of vaccine product; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 64-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 28Sep2022 as dose 3 (booster), single (Batch/Lot number: unknown) at the age of 64 years for covid-19 immunisation. The patient's relevant medical history included: "Mitral valve prolapse", start date: 1997 (unspecified if ongoing), notes: Mitral valve prolapse. There were no concomitant medications. Vaccination history included: moderna (First Dose: Lot: 004D21A), administration date: 19Jul2021, for COVID-19 immunization, reaction(s): "Fever", "COVID-19"; moderna (Second Dose: Lot: 0048F21A,), administration date: 08Sep2021, for COVID-19 immunization; Flu vaccine, for Immunization. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 28Sep2022, outcome "recovering", described as "Interchange of vaccine product"; RASH ERYTHEMATOUS (non-serious), RASH VESICULAR (non-serious), RASH PUSTULAR (non-serious), PRURITUS (non-serious) all with onset Oct2022, outcome "recovering" and all described as "Red Rashy Blistery Bumps, Itchy with Pus". Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The patient received the Pfizer Covid 19 Booster shot on 28Sep2022. The patient stated after 7-10 days, he had the vaccine, he started to get some red rashy bumps here and there on one place on his body, but there were 2-3 of them. he thought it was hives but then thought of shingles. He does not have a fever or feels bad or fatigued. It appears in different parts of my body, then it goes away and then it pops up again. Events started between 05Oct2022 to 10Oct2022, and he has had some improvement but then the next day they came back. The patient stated that his rashes do have blistering and he scratches them and gets the pus stuff out. He reported that he uses 71% alcohol when he does this and scratches just enough to get pus to flow and they go away, and the itch goes away. The patient currently has a spot on his arm that he has been trying to get the pus out for a day or 2 now. He stated he has done some research on the internet and hives don't have blisters. He stated they have found that in some people the Covid vaccines has been known to reactivate the Shingles Virus, a herpes type of virus, especially in older adults and he was 64. He stated he read people can get Shingles, he doesn't remember if he had chicken pox. The patient either had hives or Shingles in his 20s. The patient stated it has been 4-6 weeks, and he read that it should last that long, but it has been about 6 weeks and they still pop up here and there. The patient has a doctor appointment for Monday. The patient stated that he doesn't know if his type gets triggered by food or not. He ate some pizza and the next morning he had a rash again. The information on the batch/lot number for BNT162b2, BNT162b2 omi ba.4-5 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: Covid-19 test; Result Unstructured Data: Test Result:positive; Comments: Caller states 3 days after the vaccine, he developed a fever for 3 weeks and then tested positive for Covid 19.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Mitral valve prolapse
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 17.11.2022
- 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
Dizziness
Vertigo
Symptomtext
Intermittent Dizziness and vertigo since the day of. Today is the second day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure, anxiety, and arthritis.
- Andere Medikamente
- Atenolol, amlodipine, seroquel,
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 17.11.2022
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Headache
Pyrexia
Symptomtext
SEVERE CHILLS, FATIGUE, HEADACHE, FELT LIKE A HAD A FEVER BUT I DID NOT REGISTER A FEVER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- acne, pre-diabetes, hypercholesterolemia, anxiety
- Andere Medikamente
- fluoxetine, Ozempic, spironolactone, AREDS2, biotin, zinc, Vitamin D - but I did not take these the morning of the injection or the day after.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 13.11.2022
- Beginn
- 13.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Decreased appetite
Fatigue
Pain
Pyrexia
Symptomtext
101 degree F fever. Chills, severe fatigue, body aches. Low appetite. Lasted for 36 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Eggs.
- Vorherige Impfungen
- Fever, chills, fatigue, low appetite.
- Staat
- DE
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 21.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Aphasia
Blood test normal
Cellulitis
Computerised tomogram abnormal
Cough
Eye swelling
Headache
Influenza virus test negative
Oropharyngeal pain
SARS-CoV-2 test negative
Staphylococcal infection
Streptococcus test negative
Symptomtext
A week later, I had a bad headache, sore throat, and coughed all night long. The next day, I woke up and I couldn't talk. I did a rapid COVID-19 test and it was negative. I went to urgent care and took a PCR test, and it was negative. When the results came back, they told me I had a staph infection. They prescribed a steroid and an antibiotic, but I don't recall the names of them. Friday afternoon my left eye got really swollen. I went to the emergency room and was diagnosed with Cellulitis. I followed up with my doctor on Monday and she verified that I had Cellulitis and a Staph infection. I am doing better now, but I am still coughing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 28OCT2022 Rapid COVID-19 test negative; 30OCT2022 PCR COVID-19 test negative; 30OCT2022 Flu test negative; 30OCT2022 Strep test negative; 04NOV2022 Blood panel normal; 04OCT2022 CT scan infection found
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Levothyroxine; WELLBUTRIN
- Allergien
- Penicillin; wool
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 03.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
COVID-19
Chills
Cough
Fatigue
Headache
Malaise
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I started developing symptoms of COVID-19 on 10/11/2022. Tested positive for COVID-19 on 10/12/2022. I had a pounding headache; coughing; sore throat; fever of 101.0; chills; coughing; fatigue; and some abdominal pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- 10/12/2022 home COVID-19 test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- ALLEGRA; iron; vitamin D
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 7,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 03.11.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Injection site pain
Product administered to patient of inappropriate age
Symptomtext
The patient was mistakenly given COVID 19 Pfizer|BioNTech bivalent booster (gray cap) 0.3ml which is recommended for ages 12 years old and older. The patient reported tenderness around the vaccine injection site lasting for one day and has had no further complaints and is feeling well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 13.11.2022
- Impfdatum
- 07.11.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Symptomtext
Site: Itching at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 12.11.2022
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthropod bite
Blood test
Erythema
Rash
Rash pruritic
Skin warm
Urticaria chronic
Symptomtext
After about 10 to 20 minutes of receiving my booster, I experienced what looked like mosquito bites on my left wrist. This rash/reaction progressed, and since I received my vaccine, every day I break out in these red, hot, itchy flares. I believe it is chronic urticaria. I went to urgent care about a week later and was prescribed some steroids. Those worked and I stopped experiencing the flare-ups, but now I am off the meds and still experience bad flare-ups at least once or twice a day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Will get blood work done, and am visiting an allergist soon.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- none
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 11.11.2022
- Impfdatum
- 02.10.2022
- Beginn
- 02.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Incorrect dose administered
Interchange of vaccine products
Rash
Rash macular
SARS-CoV-2 test
Swelling
Symptomtext
swelling of both ankles, both knees and right elbow; rash; read blotches on ankles and blister; read blotches on ankles and blister; product=COVID 19, brand=Pfizer; prev dose brand=moderna; Moderna: 02Oct2022; Pfizer Bivalent: 02Oct2022; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 77-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 02Oct2022 at 15:00 as dose 5 (booster), single (Lot number: GJ6739) at the age of 77 years, in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 02Oct2022 as dose 4 (booster), single (Lot number: 056M21A), in arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: FLU [INFLUENZA VACCINE] taken for immunisation, on 30Sep2022 as unk, single. Vaccination history included: moderna (DOSE 1, SINGLE; Lot No: 025J20-2a; anatomical location: Arm Right, Administration Time: 04:00 PM), administration date: 28Jan2021, when the patient was 76-year-old, for Covid-19 Immunization; moderna (DOSE 2, SINGLE; Lot No: 013a2121A; anatomical location: Arm left, Administration Time: 04:00 PM), administration date: 25Feb2021, when the patient was 76-year-old, for Covid-19 Immunization; moderna (DOSE 3, SINGLE; Lot No: 066d21a; anatomical location: Arm left, Administration Time: 12:00 PM), administration date: 23Aug2021, when the patient was 76-year-old, for COVID-19 immunization. The following information was reported: INCORRECT DOSE ADMINISTERED (non-serious) with onset 02Oct2022, outcome "unknown", described as "Moderna: 02Oct2022; Pfizer Bivalent: 02Oct2022"; INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 02Oct2022 at 15:00, outcome "unknown", described as "product=COVID 19, brand=Pfizer; prev dose brand=moderna"; RASH (non-serious) with onset 03Oct2022 at 08:00, outcome "recovered"; RASH MACULAR (non-serious), BLISTER (non-serious) all with onset 03Oct2022 at 08:00, outcome "not recovered" and all described as "read blotches on ankles and blister"; SWELLING (non-serious) with onset 08Oct2022, outcome "not recovered", described as "swelling of both ankles, both knees and right elbow". The events "read blotches on ankles and blister", "swelling of both ankles, both knees and right elbow" and "rash" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of rash macular, blister, swelling, rash. Additional information: There were no known allergies. Patient received antibiotics followed by prednisone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221103; Test Name: Covid test; Test Result: Negative ; Comments: Nasal swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (if covid prior vaccination: Yes); Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 10.11.2022
- Impfdatum
- 02.11.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gait disturbance
Loss of personal independence in daily activities
Muscle spasms
Muscle tightness
Muscle twitching
Musculoskeletal stiffness
Nodule
Pain
Pain in extremity
Peripheral swelling
Pruritus
Skin warm
Sleep disorder
Weight bearing difficulty
Symptomtext
At 7:30PM, I was laying on a massage table at an appointment. I noticed my left foot started itching. I tried moving it, but it wouldn?t stop. I started feeling twitching and muscle spasms in my thigh and foot. That continued for about 30-45 minutes. It simmered down, but it started getting painful in the big toe area of my foot. When I got home, I had to take off my shoe due to the pain in my foot. I took off my sock to apply magnesium gel. I noticed my foot felt hot in the side of my foot. The magnesium gel helped with the throbbing. I also propped my foot up while I ate. After I went to bed, I woke up with an awful pain in my foot at about 04:00AM. I applied more magnesium gel and kept it propped up for the rest of the night. When I got up the next morning, it was hard to walk on my left foot. I applied more magnesium gel. I couldn't put a shoe on because my foot was swollen and very hot. When I kept my foot propped up, it hurt but I didn't need to take pain medication. On Saturday, I had an appointment with my acupuncturist and my therapeutic massage therapist. I showed her my foot. She said because of the timing of the symptoms, she thought it was due to the vaccine. She noticed my arm, thigh, and calves were swollen and tight as well. The massage therapist said I was knotted up and tight, so she worked on those areas to loosen everything up again. When they were done, I could put weight on my foot and could walk normally. It lessened the pain as well. The swelling has gone down a bit. I can bend my toes and bare weight on my foot. It's still painful, but it's not as painful as it was before the massage.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines; Breast Cancer
- Andere Medikamente
- None
- Allergien
- Codeine; Dust; Peaches; Benzine
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 01.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lethargy
Off label use
Pain
Product use issue
Pyrexia
Symptomtext
Fever, aches, lethargy; Fever, aches, lethargy; Fever, aches, lethargy; other vaccine same date product=GSK; other vaccine same date product=GSK; 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 01Nov2022 as dose 5 (booster), single (Lot number: GJ6739) at the age of 53 years intramuscular, in right 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; Covid-19 vaccine (Dose 3, unknown manufacturer), for COVID-19 immunization; Covid-19 vaccine (Dose 4, unknown manufacturer), for COVID-19 immunization. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 01Nov2022, outcome "unknown" and all described as "other vaccine same date product=GSK"; PYREXIA (non-serious), PAIN (non-serious), LETHARGY (non-serious) all with onset 02Nov2022, outcome "recovering" and all described as "Fever, aches, lethargy". Therapeutic measures were not taken as a result of pyrexia, pain, lethargy. Additional information: Location of injection for vaccine received same date: GSK - left arm. The patient was not diagnosed with COVID-10 prior to vaccination. The patient was not tested for COVID-19 since the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 7,0
- Geschlecht
- F
- Eingang
- 07.11.2022
- Impfdatum
- 05.11.2022
- Beginn
- 05.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chills
Product administered to patient of inappropriate age
Pyrexia
Symptomtext
Patient received vaccination that was not age appropriate. Patient is 7 years old but received pfizer-Bivalent for age 12+. Discovered 2 days after vaccine was administered. Patient was admitted to urgent care on 11/06/22 due to high fever and chills. Ibuprofen was prescribed by physician at Urgent care and patient is stable as of 11/07/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 31.10.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood creatine phosphokinase
C-reactive protein
Full blood count
Gait disturbance
Metabolic function test
Muscular weakness
Nausea
Pain
Pain in extremity
Platelet count
Red blood cell sedimentation rate
Sitting disability
Urine analysis
Symptomtext
Morning after injection experienced aching in left thigh around 10 am which progressed throughout the day becoming increasingly painful. No swelling or redness visible. By evening there was muscle weakness and difficulty walking. By the next morning (11/2/22) the pain was so bad I was nauseous and thought I might get sick. Great difficulty walking. Pain worse with leg abduction, sitting in chair with legs 90 degrees and walking.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- Urinalysis C Reactive Protein ESR Westergren sedimentation rate, automated Creatine Kinase Comprehensive metabolic panel CBC, Platelets
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroid Allergies Chronic urticaria (no instances since spring 2022)
- Andere Medikamente
- Armour Thyroid AM/PM Menopause Formula - Integrative Therapeutics Vitamin D Feosol Iron Estradiol Fluticasone
- Allergien
- Sulfa antibiotics Codeine Ibuprofen Omeprazole Lansoprazole
- Vorherige Impfungen
- Pfizer Covid-19 2nd dose (ER8733) given 4/7/2021 - high fever , 103+, severe headache, for two days after vaccination. April 21,
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 03.11.2022
- Impfdatum
- 29.10.2022
- Beginn
- 29.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Symptomtext
Patient came into pharmacy on 11/3/22 11:00am and notified pharmacy that he was having pain on upper part of shoulder and his back. He received a dose of the Pfizer bivalent vaccine on 10/29/22. Patient was advised to alternate between hot and cold compress around the clock and take ibuprofen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.11.2022
- Impfdatum
- 23.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 5,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Ophthalmological examination normal
Respiratory tract congestion
Symptomtext
I had a headache and congestion in the left. I contacted the nurse who told me to keep putting warm compresses for my eye and take Tylenol and Advil for my head pain. I had an appointment with eye doctor. They did a regular eye exam and there was nothing wrong with my eye. After 2 days I was much better and have sense. The eye exam I had was previously scheduled and was not for the pain. However, the doctor did not see
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Eye Exam-September 29, 2022 & October 26, 2022-Normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Rheumatoid Arthritis
- Andere Medikamente
- Vitamin D, Vitamin B
- Allergien
- Penicillin; Amoxicillin; Azithromycin; Sulfa Drugs; Tussinex;
- Vorherige Impfungen
- Shingrix-After Dose-2nd dose 2020-Fever, chills, body ache vomiting for 24 hours
- Staat
- IL
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 01.11.2022
- Impfdatum
- 25.10.2022
- Beginn
- 25.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Dizziness
Fatigue
Headache
Myalgia
Symptomtext
Chills; Joint pain; muscle pain; headache; fatigue; lightheaded; 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 female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 25Oct2022 at 15:00 as dose 4 (booster), single (Lot number: GJ6739) at the age of 45 years, in right arm for covid-19 immunisation. The patient's relevant medical history was not reported. Concomitant medication(s) included: FLU [INFLUENZA VACCINE] taken for immunisation, on 21Oct2022 as unk unk, single. 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: CHILLS (non-serious) with onset 25Oct2022 at 17:00, outcome "recovering"; ARTHRALGIA (non-serious) with onset 25Oct2022 at 17:00, outcome "recovering", described as "Joint pain"; FATIGUE (non-serious) with onset 25Oct2022 at 17:00, outcome "recovering"; HEADACHE (non-serious) with onset 25Oct2022 at 17:00, outcome "recovering"; DIZZINESS (non-serious) with onset 25Oct2022 at 17:00, outcome "recovering", described as "lightheaded"; MYALGIA (non-serious) with onset 25Oct2022 at 17:00, outcome "recovering", described as "muscle pain". Therapeutic measures were not taken as a result of chills, arthralgia, myalgia, headache, fatigue, dizziness. Additional information: Other vaccine in four weeks included Flu. Patient did not have covid prior to vaccination and did not covid tested post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 31.10.2022
- 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
Body temperature increased
Ear pain
Feeling abnormal
Injection site pain
Oral discomfort
Pain
Symptomtext
Six hours foloowing the booster the injection site was painful. Fouteen hours after shot, I felt as though I had been crushed by an elephant! By10:00 a.m. (the day after the shot) I had a temp of 101.1. Took ibuprofen the rest of day... temp lowered to 98.4 and slept well that night. Next day felt on the mend and pain was lessend with temp ~ 97.7. As I write this, I have an earache (left) and the roof of my mouth feels burnt... temp 98.1. Currently taking 200mg ibuprofen every two hours for the shooting pain in the ear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High BP Hypothyroid Diet Controlled Type2 Diabetes High LDL Low HDL
- Andere Medikamente
- Pravastatin Clonodine Levothyroxine Valzartan-HCTZ NeuraZenx Alpha Lipoic Acid Mg L-Threonate Aspirin
- Allergien
- Griseofulvin Tylenol
- Vorherige Impfungen
- Arm pain
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 20.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Lip swelling
Nasal congestion
Oral disorder
Periorbital swelling
Rash pruritic
Rash pustular
Scab
Symptomtext
Demarcated rash with itchy, crusty pustuals around the elbow. Oral cavity problems including swelling of inner lip. She also reported puffy eyes, nasal congestion, and fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- similar with first Pfizer booster, but not as severe
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 15,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abnormal faeces
COVID-19
Cough
Diarrhoea
Drainage
Gastrointestinal disorder
Headache
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
My peak symptoms were on the 21st of October, and I had a bad sore throat overnight and some coughing. On the 22nd I tested positive for COVID. I had the typical coughing, sneezing, runny nose and also a bad headache. On the 20th I also had a headache and a very sore throat. I also had clear drainage. I also noticed that my stool smelt horrible. My symptoms peaked overnight on the 21st and then on the 22nd I called my health insurance and spoke to the NP. Another symptom I had was diarrhea. I had GI problems. I attribute the GI issues to COVID, but I did not attribute the allergy symptoms to COVID at the time. I have tested negative 3 times now in a row.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 3 COVID at home test.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Pain issues; total hip replacement; High stress level; depression; anxiety.
- Andere Medikamente
- Estrogen; progesterone; allergy shots; ALLEGRA; FLONASE; eye drops; multivitamin; fish oil
- Allergien
- Seasonal allegries
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Hyperhidrosis
Muscular weakness
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Weakness-Mild, Additional Details: patient recieved vaccination at 5:25 PM . at 5:30 pm she felt weak at the knees, and was feeling faint, and was sweating, therefore EMS was called and they checked her vitals in the ambulance. Patient was awake and aware and felt better by the time the ambulance arrived.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 28.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Myalgia
Pain
Wrong product administered
Symptomtext
Severe pain in left and right hip joints; Severe soreness in left and right thigh muscles that extended down to back of knees; Severe soreness in left and right thigh muscles that extended down to back of knees; Wrong vaccine administered; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. An 80-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 06Oct2022 at 16:15 as dose 1 (bivalent), single (Lot number: GJ6739) at the age of 80 years, in left arm for covid-19 immunisation. The patient didn't receive BNT162b2 (BNT162B2). The patient's relevant medical history included: "High blood pressure" (unspecified if ongoing); "high cholesterol" (unspecified if ongoing); "slow urine flow" (unspecified if ongoing); "sluggish stool" (unspecified if ongoing). Concomitant medication(s) included: AMLODIPINE BESYLATE. Past drug history included: Known allergies: statin medications, reaction(s): "known allergies: Statin medications". The following information was reported: WRONG PRODUCT ADMINISTERED (non-serious) with onset 06Oct2022, outcome "unknown", described as "Wrong vaccine administered"; ARTHRALGIA (non-serious) with onset 11Oct2022, outcome "not recovered", described as "Severe pain in left and right hip joints"; MYALGIA (non-serious), PAIN (non-serious) all with onset 11Oct2022, outcome "not recovered" and all described as "Severe soreness in left and right thigh muscles that extended down to back of knees". Therapeutic measures were taken as a result of arthralgia, myalgia, pain. Additional information: The patient did not receive any other vaccine within four weeks. The patient did not have Covid prior to vaccination and the patient was not tested with Covid post vaccination. AE treatment: Extra Strength Pain Reliever Acetaminophen 500 mg. 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
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high; Cholesterol high; Stools abnormal; Urine flow decreased
- Andere Medikamente
- AMLODIPINE BESYLATE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 27.10.2022
- Impfdatum
- 08.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Myalgia
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
I had sore throat, congestion, runny nose, dry cough which was not productive, sneezing and muscular aches. I was in the home with someone testing positive so within 2 hours I tested positive for COVID 19 on Saturday October 23, 2022. I went to urgent care. They did not recommend any treatment since my symptoms were mild. They suggested that I take over the counter SUDAFED. My symptoms improved fast. I had improved by Sunday afternoon and by Monday I felt like most of it was gone. I feel as if I have completely recovered, the same as prior to having it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- COVID 19 home test October 23, 2022 positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Osteoporosis
- Andere Medikamente
- Bupropion; PROLIA; calcium with vitamin D; vitamin D; acyclovir; RESTASIS eye drops
- Allergien
- Morphine; codeine
- Vorherige Impfungen
- Shingles vaccine (prior to Shingrix) caused allergic reaction on my arm. This was 5 years ago.
- Staat
- -
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 19.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Rash
Rash pruritic
Varicella zoster virus infection
Symptomtext
2 days after vaccine the patient developed a rash which was itchy and then painful. On evaluation in clinic the rash was consistent with varicella zoster. Notably she has had both of her shingrix vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 15.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Muscle tightness
Osteoarthritis
Pain
Pain in extremity
X-ray of pelvis and hip abnormal
Symptomtext
It started on the next day with the usual aches and tiredness. The next day I noticed that all my muscles were still tight especially in my hip and quads area. It continued to get worse to get worse to where I was not able to do my physical therapy or the walks. It truly hurt. It was a 6 or 7 on a scale of 1-10. I took heavy dose of ibuprofen, but the pain continued. Friday was the worse. I went to the doctor, and he told me to go back and start the physical therapy again and to gradually start walking. He also advised me to continue to take the ibuprofen for pain. My pain is about a 2 in my quads and I walked this morning for a short period, so the symptoms are not gone but are getting better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Bi Lateral Hip X-ray Friday October 21, 2022 mild Osteoarthritis, no new symptoms.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Cholesterol; Osteopenia
- Andere Medikamente
- Simvastatin; alendronate sodium; ginkgo biloba; biotin; PRESERVISION AREDS 2; magnesium; calcium with vitamin D; multivitamin; CELLGEVITY
- Allergien
- Penicillin; sulfa; azithromycin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 75,0
- 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
Body temperature
Cough
Interchange of vaccine products
Investigation
Oropharyngeal discomfort
Pyrexia
SARS-CoV-2 test
Symptomtext
I started getting a sickness in my throat.; have a dry cough, like clearing my throat; I had a fever - 97.4, 99 and then this morning 99.4 ?F; I previously reacted to Moderna; I got 2 vaccines and 1 booster. This one was from Pfizer; 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 75-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 18Oct2022 at 09:45 as dose 4 (booster), single (Lot number: GJ6739) at the age of 75 years for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Moderna covid-19 vaccine (DOSE 1, SINGLE), for Covid-19 Immunization, reaction(s): "immediate reactions"; Moderna covid-19 vaccine (DOSE 2, SINGLE), for Covid-19 Immunization; Moderna covid-19 vaccine (DOSE 3 (BOOSTER), SINGLE), for COVID-19 immunization, reaction(s): "feeling funky". The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (non-serious) with onset 18Oct2022 at 09:45, outcome "unknown", described as "I previously reacted to Moderna; I got 2 vaccines and 1 booster. This one was from Pfizer"; PYREXIA (non-serious) with onset 20Oct2022, outcome "not recovered", described as "I had a fever - 97.4, 99 and then this morning 99.4 ?F"; OROPHARYNGEAL DISCOMFORT (non-serious) with onset 20Oct2022, outcome "not recovered", described as "I started getting a sickness in my throat."; COUGH (non-serious) with onset 20Oct2022, outcome "not recovered", described as "have a dry cough, like clearing my throat". Relevant laboratory tests and procedures are available in the appropriate section. Therapeutic measures were taken as a result of oropharyngeal discomfort, cough, pyrexia. Additional information: patient stated that she received the COVID-19 vaccine booster on tuesday this week (18Oct2022). she got it on tuesday at 9:45. she felt really good all day that day and also all wednesday. Then, yesterday 20Oct2022 she started getting a sickness in my throat. she had a dry cough, like clearing my throat. Yesterday she had a fever - 97.4, 99 and then this morning 99.4 ?F. she called my pharmacist and took a COVID-19 test. she tested negative twice - last night and this morning. she previously reacted to Moderna; she got 2 vaccines and 1 booster. Did have reactions, immediate reactions, to the Moderna COVID-19 Vaccine. Her first two vaccines and first booster were all the Moderna COVID-19 Vaccine. She had progressively worse side effects from those but they happened within two hours of having the shots. Her Moderna COVID-19 Vaccine Booster she had about 2 or 3 days where she was feeling funky. Her normal temp is 97.4 degrees Fahrenheit. Last night she was running a fever of 99 degrees Fahrenheit and this morning it was 99.4 degrees Fahrenheit causing her chills. Her throat does not hurt, she does not have a sore throat, her throat feels thick. She was coughing a dry cough and this was not her real voice. Took two Tylenol and was feeling so much better currently. Thinks the fever broke but she sounds ridiculous. Cough was still there and feeling of thickness was still there. Thickness started first then she had the dry cough. The thickness in her throat and the dry cough were still happening periodically, on and off. Still being effected by the fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Test Name: normal temp; Result Unstructured Data: Test Result:97.4 ?F; Comments: Her normal temp is 97.4 degrees Fahrenheit; Test Date: 20221020; Test Name: fever; Result Unstructured Data: Test Result:99 ?F; Comments: Last night she was running a fever of 99 degrees Fahrenheit; Test Date: 20221021; Test Name: fever; Result Unstructured Data: Test Result:99.4 ?F; Comments: this morning it was 99.4 degrees Fahrenheit; Test Date: 20221020; Test Name: Covid-19 Test; Test Result: Negative ; Comments: COVID-19 test. I tested negative twice - last night and this morning; Test Date: 20221021; Test Name: Covid-19 Test; Test Result: Negative ; Comments: COVID-19 test. I tested negative twice - last night and this morning
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Pain
Symptomtext
I've been experiencing a sharp, dull, and hot pain in my appendix area that lasts for several hours. The pain has been becoming more and more severe. I haven't been taking any treatment for it and my doctor has not prescribed anything yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- 19Oct2022 blood work normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes; Asthma; Von Willebrand
- Andere Medikamente
- Glyburide; metformin; JANUVIA
- Allergien
- Sulfa; anchovies
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 24.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Abdominal pain upper
Cholecystectomy
Laboratory test
Laparoscopic surgery
Nausea
Ultrasound abdomen abnormal
Symptomtext
ON 10.17.2022 PATIENT STARTED HAVING MODERATE TO SEVERE RIGHT UPPER QUADRANT EPIGASTRIC ABDOMINAL PAIN AND MILD NAUSEA. PATIENT INSTRUCTED BY HIS PCP TO COME TO THE ER. HE ENDED UP HAVING LAPAROSCOPIC CHOLECYSTECTOMY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- LABS AND ULTRASOUND 10.18.2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- ANGINA PECTORIS, ATRIAL FIBRILLATION, CORONARY ARTERY DISEASE, CAROTID STENOSIS, DEGENERATIVE DISC, HYPERLIPIDEMIA, HYPERTENSION, VENTRICULAR ECTOPY
- Andere Medikamente
- METOPROLOL, TAMSULOSIN, ATORVASTATIN, ASPIRIN, ISOSORBIDE, LISINOPRIL, REPLENEX
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 17.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Malaise
Pain
Pain in extremity
Peripheral swelling
Symptomtext
10/17/2022 in the evening when I was going to bed, my injection site was sore. And I took Tylenol. 10/18/2022- My arm was still sore. I took more Tylenol. Throughout the day, I felt achy, and I had general malaise. That evening I took more Tylenol. 10/19/2022 - I had soreness around the injection site. My arm was swollen. And I took more Tylenol. I went to see the nurse at the school I work, and she advised me to take Tylenol. I put an ice pack on it that evening. 10/20/2022- I had a headache, still swelling around the injection site. I took Tylenol this morning. It is still sore to the touch, and it is slightly red.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin B12; vitamin D3; Magnesium
- Allergien
- Sulfa
- Vorherige Impfungen
- Moderna doses 1, 2, and 3 -rash, mild fatigue for 1 day, mild redness.
- Staat
- OH
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 23.09.2022
- Beginn
- 24.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Herpes zoster
Injection site pain
Pain
Pain in extremity
Rash
Symptomtext
It started with a pain in my right shoulder as the day the went on the pain moved down my right arm and eventually moved to my thumb and index finger, then a little rash appeared that hurt but did not itch, when I went to urgent care I was diagnosed with Shingles.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Acid reflux; Atrial Fibrillation; Arthritis
- Andere Medikamente
- Furosemide; spironolactone; omeprazole; amlodipine; CALTRATE D3; PRESERVISION; women's multivitamin
- Allergien
- Amoxicillin POT clavulanate; morphine; adhesive spray; sulfamethoxazole
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye irritation
Headache
Injury corneal
Laboratory test
Lymphadenopathy
Pain in extremity
Pyrexia
Sleep disorder
Symptomtext
That night had really bad arm pain; Woke up in the middle of the night with high fever; Next morning fever was still there and my Lymph Nodes were swollen; Got better with a lingering headache; Then started having an eye irritation; Went to the Ophthalmologist and had testing and found out that my cornea had a scratch that split my cornea in half; Was prescribed HSB flareup, and had to put ointment ZIRGAN to put in my eye; Currently using ZIRGAN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Eye scan, my cornea had a scratch that split my cornea in half.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Ibuprofen
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 19.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Fatigue
Laboratory test abnormal
Malaise
Renal failure
Symptomtext
Patient reports having been recently diagnosed with kidney failure. Patient believes the symptoms were adverse reactions of her recent Pfizer Covid 19 shot given 9/19/22. Patient wanted to get Pfizer on 9/19 even though her all previous covid-shots were Moderna. Before shots were given, every questionnaire was checked: no allergies or chronic conditions; patient answered all 'no' for any precautions and contraindications; checked eligibility; last booster was 4/6/22; Patient got both flu-shot and Pfizer shot at the same visit as patient wanted. All possible common side effects were counseled and asked patient to stay near the pharmacy for 15 min to make sure if patient has no reactions. On 10/17/22, Patient visited pharmacy to report her recent symptoms; reports that she had no energy for the next few days after the two shots. Due to continuous fatigue and malaise, patient went to see her primary doctor and was diagnosed with kidney failure recently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Patient reports all related lab test done to be diagnosed with kidney failure per pt.
- Aktuelle Erkrankungen
- Patient reported no illness on Vaccine questionnaire written on 9/19/22.
- Vorgeschichte
- Patient reported chronic health conditions on Vaccine questionnaire written on 9/19/22.
- Andere Medikamente
- Patient reports taking Lisinopril 20 mg, Atorvastatin 40 mg, Synthroid 88 mcg, allopurinol 100 mg and OTC Fiber
- Allergien
- Patient reports no allergies over the phone and on Vaccine questionnaire written on 9/19/22.
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site rash
Injection site warmth
Symptomtext
PATIENT REPORTED A RASH ON ARM BELOW THE INJECTION SITE; STATED RASH WAS HOT TO TOUCH.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- -
- Andere Medikamente
- UNKNOWN
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chills
Fatigue
Headache
Oral herpes
Pyrexia
Symptomtext
Chills, Fever and totally tired for 24 hours, then warn out, feelings of headaches and chest uncomfortable and then after that resolved had three cold sores at once.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Vitamin D, Acidopholis, Vitamin B12 and Vitamin C
- Allergien
- Dairy, Penicillian, Erthromycin, Steroids
- Vorherige Impfungen
- Pfizer Booster 4/1922 24 Hours had chills, and tired and then went away.
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 04.10.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Symptomtext
Site: Bruising at Injection Site-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 16.10.2022
- Impfdatum
- 13.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Hyperhidrosis
Incontinence
Injection site pain
Lymph node pain
Lymphadenopathy
Night sweats
Pain
Pain in extremity
Pyrexia
SARS-CoV-2 test negative
Symptomtext
Headache, Chills, fever, body aches, lymph glands under arm are swollen and tender, pain at injection site, pain when raising arm. I traded off first using tylenol, then ibuprofen when tylenol didn't seem to help. The fever 100.3 finally broke on Sunday when I woke to my bed saturated with sweat. Arm pain and lymph tenderness/pain continues. Oddly, and I'm not sure if it's from the shot or not, plus I have been drinking a lot of water, but in the mornings during these fevers I actually peed myself like I was temporarily incontinent. I expect the body aches will go away. I did take a covid test, it was negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Elderberry with vitamin c and zinc, turmeric curcumin, protonix, fish oil, b12, berberine, d3
- Allergien
- None
- Vorherige Impfungen
- Similar to my second covid shot.
- Staat
- IN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Myalgia
Pyrexia
Symptomtext
About 12 hours after receiving the injection, I started having muscle aches and fever and chills. During the night the muscle aches and fever worsened and I also began to have an intense headache. The symptoms lasted for about 36 hours and then lessened. By 48 hours, most symptoms were gone, except for the headache. I treated the symptoms with acetaminophen and fluids. These are the same symptoms I had with each Covid-19 shot and also with Covid-19, itself, which I had in November of 2020.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Cholestrol, Interstitial Cycsitis
- Andere Medikamente
- Medication Strength Dosage Description Prescription Triamterene/HCTZ Capsule 37.5 mg/25 mg 1 per day, a.m. Small white capsule with black stripes Armour Thyroid Tablet 30 mg 1/day, a.m. Very small tan tablet Amitriptyline Tablet 25 mg 1/
- Allergien
- Penicillin, cyclosporins, sulfa
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 12.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Poor quality product administered
Product storage error
Symptomtext
Sore arm; stored the vial at room temperature for an extended amount of time with no protection from room light; stored the vial at room temperature for an extended amount of time with no protection from room light; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. A 36-year-old female patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 06Oct2022 at 11:50 as dose 4 (booster), 0.3 ml single (Lot number: GJ6739, Expiration Date: Dec2022) at the age of 36 years, in left deltoid for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: Covid-19 vaccine (DOSE 1, UNKNOWN MANUFACTURER, the original dose formulation), for COVID-19 Immunization; Covid-19 vaccine (DOSE 2, UNKNOWN MANUFACTURER, the original dose formulation), for COVID-19 Immunization; Covid-19 vaccine (DOSE 3 (BOOSTER), UNKNOWN MANUFACTURER), for COVID-19 Immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 06Oct2022, outcome "not recovered", described as "Sore arm"; PRODUCT STORAGE ERROR (non-serious), POOR QUALITY PRODUCT ADMINISTERED (non-serious) all with onset 06Oct2022, outcome "unknown" and all described as "stored the vial at room temperature for an extended amount of time with no protection from room light". Therapeutic measures were not taken as a result of pain in extremity. Additional information: The reporting consumer was the patient. Patient stated she was given the Pfizer-Biontech Covid bivalent vaccine today as booster (her first and only dose of the Pfizer Covid Bivalent Booster). She called because she is concerned about how the Pharmacist handled the storage of the product today that she was administered. She noticed that they stored the vial at room temperature for an extended amount of time with no protection from room light. She saw the Pharmacist drawing the Pfizer Covid Bivalent Booster using a syringe from a bottle; they put the vial in the orange bottle (like that usually hold prescription pills) with no cap and left it on a bench where she administers vaccines to people; at room temperature. Patient added that she is aware that "usually vaccines are covered." Patient said she does not know how long the Pfizer-Biontech Covid bivalent vaccine vial was at room temperature but she was at pharmacy at 11:00 and she got the dose at 11:50. She added she saw the pharmacist prepare the vaccine, "where she took it from the table." When she asked the pharmacist if the vial can be stored at room temperature, she was told yes. She mentioned she "searched online, I didn't realize they should cover the vial." Patient asked if the dose was viable, if the product is still good. She also mentioned towards the end of this report that she just started feeling a little bit of a sore arm so she might have some side effects the next day. She has not had any treatments or medical interventions relative to these events to report. She mentioned that prior to this product she had 2 of the original dose formulation and a booster but provided no further details on those products. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- 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
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 09.10.2022
- Impfdatum
- 26.09.2022
- Beginn
- 26.09.2022
- 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
Lymphadenopathy
Pain in extremity
Swelling
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Swelling of the left pectoral area, followed by a draining like sensation that resulted in a hard bump above patients left hip a couple of days later, which is now subsiding.-Mild, Systemic: Lymph Node Swelling-Mild, Additional Details: Patient explained that the day of vaccination he had soreness in his left arm, that after two days his left under arm and left pectoral area were swollen, that two days after the swelling the patient experienced what seemed like an internal drainig that resulted in a bump over his left hip he described like a cube of butter, and five days after the cube of butter formed the patient says it is about 80% better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 3,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Dizziness
Feeling drunk
Gait disturbance
Gait inability
Inner ear disorder
Nausea
Sleep disorder
Vertigo
Wheelchair user
Symptomtext
I woke up in the morning and felt extremely dizzy and lost my balance. It felt as if I had been drinking but I had not. I called and made an appointment to see my doctor. I had to use a wheelchair to get into the doctor's office I could not use my legs. She diagnosed me with vertigo and prescribed Antivert 25mg to take three times a day and some exercises to do to help realign the crystals in my inner ears. I am currently patiently waiting for the vertigo to go away. I have propped up the head of my bed to help me sleep, the nausea has subsided, I am able to read and I can "chair walk".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetes; Hypertension;
- Andere Medikamente
- Victoza; Metformin; Lisinopril, Vitamin D3; Ocuvite; Xarelto;
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 04.10.2022
- Impfdatum
- 03.10.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Pain in extremity
Symptomtext
Patient stated she is having severe pain in her right hip and leg, and it may be due to the vaccine. She received the vaccine in her left deltoid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 03.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Symptomtext
Injection site is re$, swollen, and itchy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Latanoprost
- Allergien
- Bacitracin zinc
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 02.10.2022
- Impfdatum
- 30.09.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Painful, red, swelling at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN
- Andere Medikamente
- Irbesartin Atenolol Atorvastatin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 02.10.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Systemic: Dizziness / Lightheadness-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 29.09.2022
- Impfdatum
- 24.09.2022
- Beginn
- 24.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Myalgia
Off label use
Pain in extremity
Product use issue
Symptomtext
Moderate fatigue; Arm pain; Moderate to mild myalgia; other vaccine same date product: Influenza; other vaccine same date product: Influenza; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP). A 47-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 24Sep2022 at 17:00 as dose 4 (booster), single (Lot number: GJ6739) at the age of 47 years intramuscular, in left arm for covid-19 immunisation; influenza vaccine (INFLUENZA VACCINE), on 24Sep2022 as dose 1, single (Batch/Lot number: unknown), in right arm for immunisation. The patient's relevant medical history was not reported. The patient took concomitant medications. Vaccination history included: Covid-19 vaccine (Primary immunization completed (Manufacturer Unknown)), for Covid-19 immunization; Covid-19 vaccine (DOSE 3 (BOOSTER), SINGLE (Manufacturer Unknown)), for Covid-19 immunization. The following information was reported: OFF LABEL USE (non-serious), PRODUCT USE ISSUE (non-serious) all with onset 24Sep2022, outcome "unknown" and all described as "other vaccine same date product: Influenza"; PAIN IN EXTREMITY (non-serious) with onset 24Sep2022 at 22:00, outcome "not recovered", described as "Arm pain"; FATIGUE (non-serious) with onset 24Sep2022 at 22:00, outcome "not recovered", described as "Moderate fatigue"; MYALGIA (non-serious) with onset 24Sep2022 at 22:00, outcome "not recovered", described as "Moderate to mild myalgia". Therapeutic measures were not taken as a result of fatigue, pain in extremity, myalgia. Additional Information: The patient took over the counter and prescription medications in two weeks. The patient has not been diagnosed with covid prior vaccination and has not tested for covid post vaccination. The patient has no known allergies. The patient experienced arm pain very mild on day of vaccination, then moderate the date following vaccination; moderate to mild myalgia - mild day of vaccination and moderate day following vaccination and moderate fatigue. Based on previous experience with the vaccine recipients are likely to resolve within 48-72 hours post-dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- M
- Eingang
- 28.09.2022
- Impfdatum
- 24.09.2022
- Beginn
- 24.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Myalgia
Pain in extremity
Symptomtext
Arm pain: mild on day of vaccination, moderate next morning, then mild/gone 20+ hours post -vaccination; Moderate to mild myalgia; Moderate fatigue; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). A 46-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 24Sep2022 at 17:00 as dose 4 (booster), single (Lot number: GJ6739) intramuscular, in right arm for covid-19 immunization; influenza vaccine (INFLUENZA), on 24Sep2022 as dose 1, single (Batch/Lot number: unknown), in left arm. The patient's relevant medical history included: "Known allergies: lactose intolerance" (unspecified if ongoing), notes: Known allergies: lactose intolerance. The patient took concomitant medications. Past drug history included: Known allergies: acetaminophen allergy, reaction(s): "Drug allergy", notes: Known allergies: Acetaminophen allergy. Vaccination history included: Covid-19 vaccine (Dose: 03), for Covid-19 immunization; Covid-19 vaccine (dose 2), for Covid-19 immunization; Covid-19 vaccine (dose 1), for Covid-19 immunization. The following information was reported: PAIN IN EXTREMITY (non-serious) with onset 24Sep2022 at 22:00, outcome "not recovered", described as "Arm pain: mild on day of vaccination, moderate next morning, then mild/gone 20+ hours post -vaccination"; FATIGUE (non-serious) with onset 24Sep2022 at 22:00, outcome "not recovered", described as "Moderate fatigue"; MYALGIA (non-serious) with onset 24Sep2022 at 22:00, outcome "not recovered", described as "Moderate to mild myalgia". Therapeutic measures were not taken as a result of pain in extremity, myalgia, fatigue. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Lactose intolerance (Known allergies: lactose intolerance)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 20.12.2023
- Impfdatum
- 22.09.2022
- Beginn
- 13.12.2023
- Tage bis Beginn
- 447,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
tested positive for covid; tested positive for covid; This is a spontaneous report received from a Consumer or other non HCP. A 44-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 22Sep2022 as dose 4 (booster), single (Lot number: GJ6739) at the age of 43 years intramuscular, in right arm for covid-19 immunisation; COVID-19 vaccine (COVID-19 VACCINE), as dose 1, single), as dose 2, single) and as dose 3 (booster), single) for covid-19 immunisation. The patient's relevant medical history included: "high blood pressure" (unspecified if ongoing); "afib" (unspecified if ongoing); "slightly overweight" (unspecified if ongoing). Concomitant medication(s) included: LISINOPRIL; DILTIAZEM. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 13Dec2023 at 19:00, outcome "not recovered" and all described as "tested positive for covid". The event "tested positive for covid" required physician office visit. The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (13Dec2023) Positive, notes: Covid test type post vaccination: Nasal Swab. Therapeutic measures were not taken as a result of drug ineffective, covid-19. Clinical course: Pfizer employee reported no other vaccine in four weeks. On 13Dec2023, (name) tested positive for Covid. He should have gotten a booster this year. No covid-19 prior to vaccination. No known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20231213; Test Name: Binax NOW Covid 19 Ag; Test Result: Positive ; Comments: Covid test type post vaccination: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: AFib; Blood pressure high; Overweight
- Andere Medikamente
- LISINOPRIL; DILTIAZEM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 17.11.2022
- Beginn
- 22.11.2021
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Exposure during pregnancy
Ultrasound foetal
COVID-19
Drug ineffective
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
covid test result=Positive; covid test result=Positive; brand=Pfizer/Moderna; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 32-year-old female patient (pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 17Nov2022 at 18:00 as dose 5 (booster), single (Lot number: GJ6739) at the age of 31 years, in left arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 09Apr2021 as dose 1, single (Lot number: EW0158), in left arm and on 30Apr2021 as dose 2, single (Lot number: EW0173), in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 22Nov2021 as dose 3 (booster), single (Lot number: 058H21A), in left arm and on 06Aug2022 as dose 4 (booster), single (Lot number: 051B22A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hashimotos" (unspecified if ongoing), notes: I have Hashimotos. My son only has SVT, no other issues at this time. The patient was 18 weeks pregnant at the time of exposure to elasomeran. The patient is expected to deliver a baby(s) on 14Jan2023. Concomitant medication(s) included: TDAP taken for immunisation, on 21Oct2022 as dose 1, single; LEVOTHYROXINE; BABY ASPIRIN.The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 22Nov2021, outcome "unknown", described as "brand=Pfizer/Moderna"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 17Oct2023, outcome "unknown" and all described as "covid test result=Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (17Oct2023) Positive, notes: Nasal Swab. Additional information: other medications in two weeks also included Prenatal Vit.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300351825 same reporter/drug, different patient and AE(baby/mother);US-PFIZER INC-202300351759 same reporter/patient, different drug and AE(baby/mother);
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test normal
- Hospital-Tage
- -
- Labordaten
- Test Date: 20231017; Test Name: PCR; Test Result: Positive ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hashimoto's disease (I have Hashimotos. My son only has SVT, no other issues at this time.)
- Andere Medikamente
- LEVOTHYROXINE; BABY ASPIRIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 03.11.2023
- Impfdatum
- 17.11.2022
- Beginn
- 22.11.2021
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Exposure during pregnancy
Ultrasound foetal
COVID-19
Drug ineffective
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
covid test result=Positive; covid test result=Positive; brand=Pfizer/Moderna; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 32-year-old female patient (pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 17Nov2022 at 18:00 as dose 5 (booster), single (Lot number: GJ6739) at the age of 31 years, in left arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 09Apr2021 as dose 1, single (Lot number: EW0158), in left arm and on 30Apr2021 as dose 2, single (Lot number: EW0173), in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 22Nov2021 as dose 3 (booster), single (Lot number: 058H21A), in left arm and on 06Aug2022 as dose 4 (booster), single (Lot number: 051B22A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Hashimotos" (unspecified if ongoing), notes: I have Hashimotos. My son only has SVT, no other issues at this time. The patient was 18 weeks pregnant at the time of exposure to elasomeran. The patient is expected to deliver a baby(s) on 14Jan2023. Concomitant medication(s) included: TDAP taken for immunisation, on 21Oct2022 as dose 1, single; LEVOTHYROXINE; BABY ASPIRIN.The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 22Nov2021, outcome "unknown", described as "brand=Pfizer/Moderna"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 17Oct2023, outcome "unknown" and all described as "covid test result=Positive". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (17Oct2023) Positive, notes: Nasal Swab. Additional information: other medications in two weeks also included Prenatal Vit.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300351825 same reporter/drug, different patient and AE(baby/mother);US-PFIZER INC-202300351759 same reporter/patient, different drug and AE(baby/mother);
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test normal
- Hospital-Tage
- -
- Labordaten
- Test Date: 20231017; Test Name: PCR; Test Result: Positive ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hashimoto's disease (I have Hashimotos. My son only has SVT, no other issues at this time.)
- Andere Medikamente
- LEVOTHYROXINE; BABY ASPIRIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 26.10.2023
- Impfdatum
- 09.10.2022
- Beginn
- 19.05.2023
- Tage bis Beginn
- 222,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Drug ineffective
Interchange of vaccine products
SARS-CoV-2 test
Symptomtext
covid-19; covid-19; Vaccine Brand: Pfizer / BioNTech, Vaccine Administration date: 09Oct2022, Vaccine Dose number: 5, Vaccine Brand: Moderna,Vaccine Administration date: 19May2023; 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 71-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 09Oct2022 as dose 5 (booster), single (Lot number: GJ6739), in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 19May2023 as dose 6 (booster), single (Lot number: AS718QB), 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 had no relevant medical history. The patient has no known allergies. There were no concomitant medications. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 19May2023, outcome "recovered", described as "Vaccine Brand: Pfizer / BioNTech, Vaccine Administration date: 09Oct2022, Vaccine Dose number: 5, Vaccine Brand: Moderna,Vaccine Administration date: 19May2023"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Oct2023, outcome "recovered" (16Oct2023) and all described as "covid-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (16Oct2023) Negative; (21Oct2023) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. The patient took Paxlovid as treatment from 09Oct2023 to 14Oct2023. No follow-up attempts are possible. No further information is expected.; Sender's Comments: Based on available information, a lack of efficacy under interchange of vaccine products with the suspect vaccine BNT162B2 in this patient cannot be completely excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20231016; Test Name: COVID; Test Result: Negative ; Test Date: 20231021; Test Name: COVID; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: none
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 10.10.2023
- Impfdatum
- 16.11.2022
- Beginn
- 25.09.2023
- Tage bis Beginn
- 313,0
- 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 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 16Nov2022 as dose 5 (booster), single (Lot number: GJ6739) at the age of 69 years, in left arm for covid-19 immunisation; bnt162b2 (BNT162B2), on 08Jul2022 as dose 4 (booster), single (Lot number: FP7139) 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: "Parkinson's Disease" (unspecified if ongoing); "osteoporosis" (unspecified if ongoing). Concomitant medication(s) included: BUPROPION, start date: Oct2012; CARBIDOPA/LEVODOPA, start date: Oct2016; PRAMIPEXOLE, start date: Oct2014; RASAGILINE, start date: Oct2014. Past drug history included: Amantidine base, reaction(s): "Known allergies: Amantidine base". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 25Sep2023, outcome "not recovered" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (25Sep2023) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19 which includes paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230925; Test Name: COVID-19 Test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Osteoporosis; Parkinson's disease
- Andere Medikamente
- BUPROPION; CARBIDOPA/LEVODOPA; PRAMIPEXOLE; RASAGILINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 19.09.2023
- Impfdatum
- 22.09.2022
- 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
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Nurse). The reporter is the patient. A 54-year-old female patient (not pregnant) received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 22Sep2022 as dose 5 (booster), single (Lot number: GJ6739) at the age of 53 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 included: "hypothyroidism" (unspecified if ongoing); "htn" (unspecified if ongoing); "IDDM" (unspecified if ongoing). Known allergies reported as none. The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "recovering" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19 which included COVID 19 Treatment from 07Sep2023 to 11Sep2023.; Sender's Comments: Based on available information, a lack of efficacy with the suspect vaccine bnt162b2, bnt162b2 omi ba.4-5 in this patient cannot be completely excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypertension; Hypothyroidism; IDDM
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 18.09.2023
- Impfdatum
- 11.10.2022
- 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
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Nurse). 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 11Oct2022 as dose 4 (booster), single (Lot number: GJ6739) at the age of 70 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 had no relevant medical history. 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 "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19 with Paxlovid from 02Sep2023 to 06Sep2023.; Sender's Comments: Based on available information, a lack of efficacy with the suspect vaccine bnt162b2, bnt162b2 omi ba.4-5 in this patient cannot be completely excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 11.09.2023
- Impfdatum
- 07.11.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
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 15-year-old male patient received bnt162b2, bnt162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 07Nov2022 as dose 4 (booster), single (Lot number: GJ6739) at the age of 14 years for covid-19 immunisation; bnt162b2 (BNT162B2), on 17May2021 as dose 1, single (Lot number: EW0179), on 21Jun2021 as dose 2, single (Lot number: EW0191) and on 31May2022 as dose 3 (booster), single (Lot number: FM7553) for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "obesity" (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 "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: Patient had no known allergies. Patient received Paxlovid treatment from 29Aug2023 to 03Sep2023.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300295414 same patient, different drug and different AE.;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma; Obesity
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 15.08.2023
- Impfdatum
- 21.11.2022
- 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
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 77-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 21Nov2022 at 13:00 as dose 4 (booster), single (Lot number: GJ6739) at the age of 76 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: "Heart patient" (unspecified if ongoing). Concomitant medication(s) included: SIMVASTATIN, start date: 15Nov2000; TAMSULOSIN, start date: 01Oct2010; ESCITALOPRAM, start date: 01Mar2017. Past drug history included: Morphine, reaction(s): "Drug allergy". 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, notes: Treatment of COVID-19; (10Aug2023) negative, notes: tested negative on the 7th day; (11Aug2023) positive, notes: tested positive in the morning of the 8th day. Therapeutic measures were taken as a result of drug ineffective, COVID-19. Additional information: the patient took Paxlovid for 5 days, started feeling better on the 3rd day, and tested negative on the 7th day. He tested positive on the morning of the 8th day, not feeling well again. He had the same symptoms prior to taking Paxlovid.; Sender's Comments: Based on available information, a lack of efficacy with the suspect vaccine BNT162B2 in this patient cannot be completely excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID test; Test Result: Positive ; Comments: Treatment of COVID-19; Test Date: 20230810; Test Name: COVID test; Test Result: Negative ; Comments: tested negative on the 7th day; Test Date: 20230811; Test Name: COVID test; Test Result: Positive ; Comments: tested positive in the morning of the 8th day
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Heart disorder
- Andere Medikamente
- SIMVASTATIN; TAMSULOSIN; ESCITALOPRAM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- -
- Geschlecht
- F
- Eingang
- 14.08.2023
- Impfdatum
- 03.11.2022
- Beginn
- 03.11.2022
- 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
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; Moderna= 01Jul2022/ Pfizer= 03Nov2022; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 45-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 03Nov2022 at 15:30 as dose 5 (booster), single (Lot number: GJ6739), in left arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 19Mar2021 at 12:30 as dose 1, single (Lot number: 04SA21A), in left arm, on 16Apr2021 at 12:30 as dose 2, single (Lot number: 042B21A), in left arm, on 04Nov2021 at 15:00 as dose 3 (booster), single (Lot number: 071F21A), in left arm and on 01Jul2022 as dose 4 (booster), single (Lot number: 014B22A), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Chronic hives (autoimmune)", start date: Jan2010 (unspecified if ongoing), notes: chronic hives (autoimmune) diagnosed Jan2010; "Outdoor allergies" (unspecified if ongoing). Concomitant medication(s) included: ADVIL [IBUPROFEN] taken for urticaria, start date: 31Jul2023, stop date: 03Aug2023; CLARITINE, start date: May2023, stop date: 02Aug2023; NATURE'S WAY ACTIVATED CHARCOAL, start date: 02Aug2023, stop date: 04Aug2023; ZYRTEC [CETIRIZINE HYDROCHLORIDE] taken for hypersensitivity, start date: Jan2010, stop date: 02Aug2023; ZINC. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 03Nov2022 at 15:30, outcome "unknown", described as "Moderna= 01Jul2022/ Pfizer= 03Nov2022"; DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 30Jul2023, outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (31Jul2023) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. COVID-19 Treatment included Paxlovid from 01Aug2023 to 05Aug2023. Clinical course: Tested positive at home initially Mon 31Jul2023 after sore throat started 30Jul2023 and we learned of an exposure. Symptoms worsened, got Paxlovid Tues 01Aug2023, took it through the entire course on Sat 05Aug2023. Tested using throat-then-nose swab as recommended by epidemiologists. All at-home rapid tests were BinaxNow; Paxlovid given after in-office rapid test positive at [Name-withheld] in [Name], MD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230731; Test Name: Covid Home Test (BinaxNow); Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy; Chronic urticaria (chronic hives (autoimmune) diagnosed Jan2010)
- Andere Medikamente
- ADVIL [IBUPROFEN]; CLARITINE; NATURE'S WAY ACTIVATED CHARCOAL; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; ZINC
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 09.08.2023
- Impfdatum
- 21.10.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 28,0
- Dosis
- 4
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Biopsy skin abnormal
Micrographic skin surgery
Skin lesion
Squamous cell carcinoma of skin
Symptomtext
3 lesions on lower left leg--non-healing. Seen in Urgent Care 3/13/23. Referred to Dermatologist for biopsy. Results of biopsies: Invasive Squamous Cell Carcinoma, well differentiated with Keratoacanthoma-like features Mohs surgery performed on 2 lesions on 4/10/2023 Cauterization done on 3rd lesion on 7/19/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy skin abnormal
- Hospital-Tage
- -
- Labordaten
- Left distal pretibial region, biopsy by shave method Left ankle biopsy by shave method Left ankle biopsy by shave method Results: invasive squamous cell carcinoma, well differentiat
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- osteo-arthritis, episodic bronchitis
- Andere Medikamente
- Fluoxetine 20 mg. daily; Cal.Mg.Zinc; Lysine; Vit.D3;curcumin
- Allergien
- PCN, Codeine, Demerol
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- F
- Eingang
- 09.08.2023
- Impfdatum
- 27.11.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- 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 contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 27Nov2022 as dose 5 (booster), single (Lot number: GJ6739) for covid-19 immunisation; BNT162b2 (BNT162B2), on 18Jan2021 as dose 1, single (Lot number: EL3248), on 08Feb2021 as dose 2, single (Lot number: EM9810), on 02Nov2021 as dose 3 (booster), single (Lot number: FF2590) and on 11May2022 as dose 4 (booster), single (Lot number: FP4554) for covid-19 immunisation. The patient's relevant medical history included: "COVID-19" (unspecified if ongoing); "Graves Disease" (unspecified if ongoing); "Hypertension" (unspecified if ongoing); "Hyperlipidemia" (unspecified if ongoing); "Fibromyalgia" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Hydroxychloridine, reaction(s): "Known allergies: Hydroxychloridine"; Morphine, reaction(s): "Known allergies: Morphine"; Codeine, reaction(s): "Known allergies: Codeine"; Iodine, reaction(s): "Known allergies: Iodine"; Plaquenil, reaction(s): "Known allergies: Plaquenil"; Tramadol, reaction(s): "Known allergies: Tramadol"; Amitriptyline, reaction(s): "Known allergies: Amitriptyline". The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 2023, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of vaccination failure, covid-19. The patient started the first dose of Paxlovid since 31Jul2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19; Fibromyalgia; Graves' disease; Hyperlipidemia; Hypertension
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 31.07.2023
- Impfdatum
- 08.12.2021
- Beginn
- 17.03.2023
- Tage bis Beginn
- 464,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial flutter
Obstructive sleep apnoea syndrome
Symptomtext
G47.33 ADULT OBSTRUCTIVE SLEEP APNEA 2/14/2023 UNSPECIFIED ATRIAL FLUTTER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial flutter
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 17.07.2023
- Impfdatum
- 12.10.2022
- Beginn
- 15.02.2023
- Tage bis Beginn
- 126,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Angina pectoris
Symptom recurrence
Symptomtext
STABLE ANGINA ANGINA, UNSPECIFIED 2/6/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Angina pectoris
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 11.07.2023
- Impfdatum
- 03.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. An 81-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 03Oct2022 at 15:00 as dose 5 (booster), single (Lot number: GJ6739) at the age of 80 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 included: "Known allergies: Sulfa" (unspecified if ongoing), notes: Known allergies: Sulfa; "Hypertension" (unspecified if ongoing); "Migraines" (unspecified if ongoing); "Arthritis" (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 "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Additional information: The patient was treated with Paxlovid from 28Jun2023 to 02Jul2023 for the treatment of Covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Arthritis; Hypertension; Migraine; Sulfonamide allergy (Known allergies: Sulfa)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 21.06.2023
- Impfdatum
- 20.12.2022
- Beginn
- 08.02.2023
- Tage bis Beginn
- 50,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Nasopharyngitis
No adverse event
SARS-CoV-2 test positive
Symptomtext
I did not have an adverse reaction to the vaccine. I tested positive for COVID-19 on 02/08/2023. I felt like I had a mild cold. I contacted my doctor via telehealth, and I got a prescription for Paxlovid. I tolerated the medication without any complications. As of today, I am feeling better with no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 08FEB2023 COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes; Sleep Apnea; Obese
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 15.06.2023
- Impfdatum
- 01.01.2023
- Beginn
- 13.04.2023
- Tage bis Beginn
- 102,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 8/14/21 Lot# 091D; Moderna 9/11/21 lot# 052E21A; Pfizer 1/1/23 Lot# GJ6739
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 31.05.2023
- Impfdatum
- 01.05.2023
- Beginn
- 26.05.2023
- Tage bis Beginn
- 25,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Second Bivalent booster given. Clinic was unaware of 10/2022 bivalent booster that the patient had received and mom did not disclose until a follow up phone call was made 5 days later to discuss lab results (unrelated to patient's vaccine). It was during this phone call that mom disclosed patient's vaccine that she received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 93,0
- Geschlecht
- M
- Eingang
- 31.05.2023
- Impfdatum
- 23.05.2023
- Beginn
- 23.05.2023
- Tage bis Beginn
- 0,0
- Dosis
- 7+
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Extra dose given, prior additional booster given on 5/3/23 (same vaccine)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Alzheimer, Bi inguinal hernia, hemorrhoids, atrial flutter, iron deficiency, CKD, HTN, osteoarthritis, edema
- Andere Medikamente
- Acetaminophen, Albuterol, Apixaban, Carboxymethylcellulose, Cholecalciferol, Docusate, Donepezil, Epoetin Alpha, Ferrous sulfate, furosemide, hydralazine, lactulose, lidocaine, Mag -al, Mirtazapine, Olanzapine, Omeprazole, Patiromer Calcium
- Allergien
- Amlodipine, Terazosin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 27.05.2023
- Impfdatum
- 24.11.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 24Nov2022 as dose 4 (booster), single (Lot number: GJ6739) at the age of 68 years for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "No" (unspecified if ongoing), notes: Known allergies: No, Other medical history: Looking at the patient's meds, you can probably figure it out. 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 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Anti-viral details: Product: COVID 19 Treatment, brand: Pfizer, from 20May2023 to 21May2023 orally. 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: No, Comment: Known allergies: No Other medical history: Looking at the patient's meds, you can probably figure i
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 06.05.2023
- Impfdatum
- 16.02.2023
- Beginn
- 16.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 06.05.2023
- Impfdatum
- 16.02.2023
- Beginn
- 16.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 06.05.2023
- Impfdatum
- 16.02.2023
- Beginn
- 16.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 06.05.2023
- Impfdatum
- 16.02.2023
- Beginn
- 16.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 06.05.2023
- Impfdatum
- 16.02.2023
- Beginn
- 16.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 06.05.2023
- Impfdatum
- 16.02.2023
- Beginn
- 16.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 06.05.2023
- Impfdatum
- 16.02.2023
- Beginn
- 16.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 06.05.2023
- Impfdatum
- 16.02.2023
- Beginn
- 16.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 06.05.2023
- Impfdatum
- 16.02.2023
- Beginn
- 16.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 06.05.2023
- Impfdatum
- 16.02.2023
- Beginn
- 16.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 06.05.2023
- Impfdatum
- 16.02.2023
- Beginn
- 16.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 06.05.2023
- Impfdatum
- 16.02.2023
- Beginn
- 16.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 03.05.2023
- Impfdatum
- 06.10.2022
- Beginn
- 22.04.2023
- Tage bis Beginn
- 198,0
- 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 2/24/21 Lot# EN6200; Pfizer 3/17/21 Lot# ER2613; Pfizer 10/4/21 Lot# 30145BA; Pfizer 4/23/22 Lot# FM9992; Pfizer 10/6/22 LOt# GJ6739
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.05.2023
- Impfdatum
- 25.10.2022
- Beginn
- 02.03.2023
- Tage bis Beginn
- 128,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Influenza A virus test negative
Influenza B virus test
Nasal congestion
Productive cough
Rhinorrhoea
SARS-CoV-2 RNA
SARS-CoV-2 test positive
Symptomtext
On March 2, 2023, I had cough and heavy nasal discharge. We went to the store and picked up over the counter medication, ibuprofen, FLONASE for symptom relief. We thought we were having allergies. We decided to go to the clinic to go see the doctor on 03/04/2023. They tested us for COVID-19 and it was a strong positive and for Flu and it was negative. The doctor said he could prescribe the PAXLOVID but he did not recommend it because of my health condition, and I was not that sick. And he said stay quarantined for the next 5 days. I had a productive cough, and I had an extreme amount of nasal discharge. The nasal discharge was not green it was just regular. I also had nasal congestion. I did not have a fever. I did not lose my sense of smell and taste. Having as many shots that I had, I felt it kept my COVID-19 infection from getting worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 04MAR2023 COVID-19 Component SARS-2 RNA positive; 04MAR2023 Influenza A and B negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Crohn's Disease; Colostomy; Hashimoto's Thyroiditis; Glaucoma
- Andere Medikamente
- ARMOUR THYROID pill; fish oil capsules; turmeric; multivitamin; COSOPT eye drops; latanoprost eye drops
- Allergien
- Penicillin; REMICADE; steroid sensitive; cipro; erythromycin; sulfa drugs
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 26.04.2023
- Impfdatum
- 25.10.2022
- Beginn
- 08.03.2023
- Tage bis Beginn
- 134,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Nasopharyngitis
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
I had a breakthrough case of Covid-19 symptoms, started Monday, tested positive Wednesday felt like I had a cold.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- GERD; Diabetes; High Cholesterol; High blood Pressure
- Andere Medikamente
- Metformin; LEXAPRO; PRILOSEC; LIPITOR RYBELSUS; lisinopril; multivitamin
- Allergien
- Tetracycline; codeine; tramadol
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 25.04.2023
- Impfdatum
- 18.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
CONTINUOUS TINNITUS. MOSTLY IN RIGHT EAR. IT'S GETTING WORSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- NONE yet
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- osteoarthritis
- Andere Medikamente
- Levothyroxine, Duloxetine, Valsartan, Gabapentin, Wellbutrin
- Allergien
- seasonal only
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 25.04.2023
- Impfdatum
- 24.10.2022
- Beginn
- 01.04.2023
- Tage bis Beginn
- 159,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bronchitis
Cough
Respiratory disorder
Rhinorrhoea
SARS-CoV-2 test negative
Sneezing
Throat irritation
Symptomtext
4/1/23 I started with a scratchy sore throat. I then started sneezing a lot, runny nose and all upper respiratory. Then it went from a dry progressive cough to a croupy cough. I took an at home COVID test on 4/5/23 and it was negative. I was diagnosed with bronchitis and started on azithromycin on 4/11/23. It ran its course.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bronchitis
- Hospital-Tage
- -
- Labordaten
- 5APR23 at home COVID test negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoarthritis; HTV
- Andere Medikamente
- Modafinil; RESTASIS; RETINA A; PEPCID; valsartan; valacyclovir; meloxicam; potassium chloride; metoprolol; LASIX; rosuvastatin; multivitamin; fiber gummies; vitamin D3; calcium carbonate
- Allergien
- Adhesive tape
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 18.01.2023
- Beginn
- 18.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 09.01.2023
- Beginn
- 09.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
no signs & symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 04.11.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
no signs & symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 04.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
no signs & symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 18.04.2023
- Impfdatum
- 16.10.2022
- Beginn
- 24.02.2023
- Tage bis Beginn
- 131,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Bronchitis
Chest X-ray normal
Cough
Influenza virus test negative
Laboratory test normal
Respiratory syncytial virus infection
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test negative
Symptomtext
On Feb 24th, 2023, I started with cough, running nose and congestion, and it kept getting worst. I had things to do, on Monday March 6th I went to Urgent Care. I had a COVID-19 Test and a Flu test and both were negative; they gave me antibiotic I took antibiotic for 10 days and was diagnosed with Bronchitis. Then I went to see my doctor because I continued with running nose, deep cough, she prescribed medicine, an inhaler and cough medicine. I got better after that, but the cough went to allergies, she thinks I have RSV.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bronchitis
- Hospital-Tage
- -
- Labordaten
- 06MARCH2023 - COVID-19 Test - Negative; 06MARCH2023 - FLU Test - Negative; 27MARCH2023 - Chest X-Ray - Normal; 27MARCH2023 - Lab Work - Normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetes, Hypertension, Overweight
- Andere Medikamente
- Lipitor; Trazodone; Lexapro; Trospium ; Lisinopril; Hydrochlorothiazide; Metoprolol; Fish Oil; Calcium; Vitamin D; Magnesium; Aleve; Multi Vitamin; Claritin
- Allergien
- Tree Nuts; Seasonal Allergies
- Vorherige Impfungen
- COVID-19 Dose 1; 2021; Fatigue, fever for a couple of days.
- Staat
- NC
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 08.10.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 80,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deafness unilateral
Hypoacusis
Magnetic resonance imaging
Symptomtext
12/27/2022 I've lost hearing in left and the right ear has been restricted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deafness unilateral
- Hospital-Tage
- -
- Labordaten
- MRI
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Arthritis; Fibromyalgia; Brain tumor
- Andere Medikamente
- Losartan; Potassium; Rosuvastatin; Oxybutynin; Primidone; Duloxetine; Lactaid; Fish oil; Calcium; Multivitamin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 06.04.2023
- Impfdatum
- 30.09.2022
- Beginn
- 14.03.2023
- Tage bis Beginn
- 165,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Anticoagulant therapy
Burning sensation
Computerised tomogram abnormal
Echocardiogram abnormal
Full blood count abnormal
Grip strength decreased
Magnetic resonance imaging abnormal
Scan with contrast abnormal
Therapy change
Transient ischaemic attack
Symptomtext
During physical therapy on got a sharp burning sensation down my neck. When I tried to make note of this for my physical therapist, I could not hold a pen to write. I went to the emergency room they ran a CT scan both with and without contrast, an MRI, an Echocardiogram, CBC all tests show I positive for Transient ischemic attack. I was started on a regimen of baby aspirin, increase my atorvastatin that I had started in October. I was advised to stop the hormone replacement therapy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anticoagulant therapy
- Hospital-Tage
- 1,0
- Labordaten
- 14MAR2023 CT scan with contrast - Transient ischemic attack; 14MAR2023 CT scan without contrast - Transient ischemic attack; 14MAR2023 Echocardiogram - Transient ischemic attack; 14MAR2023 MRI - Transient ischemic attack; 14MAR2023 CBC - positive for Transient ischemic attack
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Levothyroxine; Estradiol Patch; Progesterone; Over the counter allergy pill and nasal spray; Multivitamin; Vitamin E; Calcium; Biotin
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 05.04.2023
- Impfdatum
- 12.10.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 50,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac monitoring abnormal
Heart rate increased
Symptomtext
I had Rapid heart rate, and its all sinus rhythm. I was treated with beta blockers and metoprolol which didn't work. I kept having pulse rates over 100bpm. The cardiologist put a monitor on my heart, I had constant rapid heart for a week so he changed my beta blocker to nancadolol, which partially controlled my rapid pulse. I still have high heart rate but less than before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac monitoring abnormal
- Hospital-Tage
- -
- Labordaten
- Yes; Not Listed
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Yes; Not Listed
- Andere Medikamente
- Yes; Not listed
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 05.04.2023
- Impfdatum
- 20.10.2022
- Beginn
- 01.10.2022
- 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
No adverse event
Symptomtext
Patient was given Bivalent as first dose in the Pfizer covid series, I spoke with the manufacturer, they referred me to the CDC for dosing recommendations. The CDC recommendation is to count the Bivalent given by mistake as the first dose in the regular series, do the monovalent as the second dose and the 3rd dose Bivalent on the regularly recommended time intervals. Patient's parent notified of the recommendations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None required, no adverse reactions from the patient.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 04.04.2023
- Impfdatum
- 28.10.2022
- Beginn
- 03.04.2023
- Tage bis Beginn
- 157,0
- 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 Pfizer 4/10/21 Lot# Ew0158; Pfizer 5/1/21 Lot# EW0176; Pfizer 12/15/21 Lot# FH8027; Pfizer 10/28/22 Lot# GJ6739
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 30.03.2023
- Impfdatum
- 28.12.2022
- Beginn
- 23.01.2023
- Tage bis Beginn
- 26,0
- Dosis
- 5
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test abnormal
Chemotherapy
Laboratory test abnormal
Myeloid leukaemia
Transfusion
Symptomtext
It's possible that since I was diagnosed back in November 2022 with a blood issue, I may have had the leukemia back then even sooner. The diagnosis was after my visit in January with my doctor several days later. They were analyzing blood tests. That visit was on 01/23/2023. That's the day the lab results became available and they determined I had myeloid leukemia later that week. They had called me on 01/26 and let me know about the diagnosis. I went for bone marrow testing a week later then went to see other specialists as well. I started chemotherapy on 02/07/2023 through 02/13/2023. It was 4 days on weekdays and that Monday was my last chemo treatment at that point. Since then, I am continuing to be treated for the leukemia. I recently had an ER visit just as a concern for my condition. I went to the ER on 03/10/2023 and I had a second round of chemo right around at that point. During this time, we've had a few medications added which are DACOGEN which is the weeks worth of chemotherapy, VENCLEXTA, doxycycline HYC, and an antiviral acyclovir. I've also received transfusions on an ongoing basis as needed. The leukemia has improved recently. At the time of detection it was at 52%, but recently it has gone down to 5%.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test abnormal
- Hospital-Tage
- -
- Labordaten
- November 2022 blood tests; January 2023 blood tests; 30JAN2023 Bone marrow testing, diagnosed leukemia; 28FEB2023 Bone marrow testing; 27MAR2023 Bone marrow testing
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; Atrial Fibrillation; Pacemaker
- Andere Medikamente
- Potassium chloride; amlodipine; furosemide; lisinopril; amiodarone; ELIQUIS; finasteride; CLARITIN; MIRALAX; CULTURELLE; PREVAGEN; vitamin D3
- Allergien
- Clindamycin; peanut butter; seasonal allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 30.03.2023
- Impfdatum
- 28.09.2022
- Beginn
- 28.03.2023
- Tage bis Beginn
- 181,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
I suffer from Chronic Fatigue. I was first diagnosed one or two years ago. I need to pace myself or else I crash, It will get bad enough that I cannot move, and my brain does not function. This particular appoint is just a regular appoint I have with a therapist. I do also have an immune issue and with that cervical pain and neck issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Fatigue; Primary Immune Deficiency, Chronis Sinusitis; Sleep Apnea; High Cholesterol; Cervical Arthritis with Nerve Pain, Osteopenia
- Andere Medikamente
- Probiotic; multivitamin; calcium; yeast probiotic; azithromycin; D2; duloxetine; modafinil; meloxicam; mupirocin ointment; famotidine; pregabalin; ASTARPRO OTC; budesonide; sinus rinse; coleopteran; montelukast; simvastatin; TYLENOL
- Allergien
- Erythromycin; LEVAQUIN; methyltrienolone; all steroids; sulfa; BACTRIM; doxycycline; dicyclomine
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 30.03.2023
- Impfdatum
- 26.09.2022
- Beginn
- 11.01.2023
- Tage bis Beginn
- 107,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
SARS-CoV-2 test positive
Symptomtext
01/11/2023 I was coughing, I took a COVID-19 home test and it was positive. 01/12/2023 I contacted urgent care and was prescribed a course of PAXLOVID. I felt better after the third day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 11Jan2023 COVID-19 home test positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Levothyroxine; atorvastatin; lisinopril; hydrochlorothiazide; baby aspirin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 29.03.2023
- Impfdatum
- 22.09.2022
- Beginn
- 26.03.2023
- Tage bis Beginn
- 185,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Productive cough
SARS-CoV-2 test negative
Symptomtext
I had some coughing up clear phlegm and sneezing. I took a COVID-19 on 03/27/2023, but the results came back negative. I called my doctor where I received a prescription for Benzoate and Bactrim DS to settle my symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Productive cough
- Hospital-Tage
- -
- Labordaten
- 27MAR2023 -- COVID-19 Test - Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Omeprazole; Olmesartan; Amlodipine; Claritin; Saline Nasal Spray
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.03.2023
- Impfdatum
- 23.01.2023
- Beginn
- 23.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Bivalent vaccine given too early
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 23.03.2023
- 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
Inappropriate schedule of product administration
Symptomtext
Received bivalent booster 6 weeks after primary series completed. Outcome unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 21.03.2023
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Wrong product administered
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; vaccine lot number=GJ6739/ vaccine dose number=1; 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 05Oct2022 as dose 1, single (Lot number: GJ6739) at the age of 59 years, in right arm for covid-19 immunisation.The patient didn't receive BNT162b2 (BNT162B2). The patient had no relevant medical history. The patient's concomitant medications were not reported. The following information was reported: WRONG PRODUCT ADMINISTERED (non-serious) with onset 05Oct2022, outcome "unknown", described as "vaccine lot number=GJ6739/ vaccine dose number=1"; 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: (unspecified date) Positive, notes: COVID 19 Treatment; (Mar2023) Negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. clinical course: patient had no Known allergies reported. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 Test; Test Result: Positive ; Comments: COVID 19 Treatment; Test Date: 202303; Test Name: Covid-19 Test; Test Result: Negative
- 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
- -
- Staat
- MD
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 17.03.2023
- Impfdatum
- 15.12.2022
- Beginn
- 08.03.2023
- Tage bis Beginn
- 83,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Lack of effect (vaccine did not provide coverage against infection and illness for at least 3 full months). Symptomatic 08Mar2023 and positive at-home test on Friday 10Mar2023; Lack of effect (vaccine did not provide coverage against infection and illness for at least 3 full months). Symptomatic 08Mar2023 and positive at-home test on Friday 10Mar2023.; This is a spontaneous report received from contactable reporter(s) (Pharmacist). The reporter is the patient. A 41-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 15Dec2022 as dose 4 (booster), single (Lot number: GJ6739) at the age of 41 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: "Raynaud's Syndrome" (unspecified if ongoing); "Seasonal Allergies" (unspecified if ongoing); "known allergies: PCN" (unspecified if ongoing). Concomitant medication(s) included: PATANOL; ATROVENT; ALLEGRA [LEVOCETIRIZINE DIHYDROCHLORIDE]; ADALAT. The following information was reported: DRUG INEFFECTIVE (medically significant) with onset 08Mar2023, outcome "recovering", described as "Lack of effect (vaccine did not provide coverage against infection and illness for at least 3 full months). Symptomatic 08Mar2023 and positive at-home test on Friday 10Mar2023"; COVID-19 (medically significant) with onset 08Mar2023, outcome "recovering", described as "Lack of effect (vaccine did not provide coverage against infection and illness for at least 3 full months). Symptomatic 08Mar2023 and positive at-home test on Friday 10Mar2023.". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (10Mar2023) Positive, notes: Nasal Swab. Therapeutic measures were taken as a result of drug ineffective, covid-19. Facility type vaccine: Pharmacy or Drug Store. AE treatment: Motrin, Tylenol, Sudafed, Atrovent. Patient did not have COVID prior vaccination.; Sender's Comments: Based on available information, a possible contributory role of the subject vaccine cannot be excluded for suspected LOE. There is limited information provided in this report. This case will be reassessed upon receipt of follow-up information. 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
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230310; Test Name: COVID-19 At-Home Test; Test Result: Positive ; Comments: Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Penicillin allergy; Raynaud's syndrome; Seasonal allergy
- Andere Medikamente
- PATANOL; ATROVENT; ALLEGRA [LEVOCETIRIZINE DIHYDROCHLORIDE]; ADALAT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 60,0
- Geschlecht
- U
- Eingang
- 17.03.2023
- Impfdatum
- 31.08.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 92,0
- 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 60-year-old patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 31Aug2022 as dose 5 (booster), single (Lot number: Gj6739) at the age of 60 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 31Jul2022 as dose 4 (booster), single (Lot number: Fj4991) for covid-19 immunisation; BNT162b2 (BNT162B2), on 16Mar2021 as dose 1, single (Batch/Lot number: unknown), in right arm, on 09Apr2021 as dose 2, single (Batch/Lot number: unknown), in right arm and on 01Feb2022 as dose 3 (booster), single (Lot number: Fg3527), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Nerve damage" (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 Dec2022, outcome "unknown" and all described as "Treatment of COVID-19". The patient was treated with Paxlovid from 22Dec2022 to 26Dec2022. 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-202300108245 same patient/vaccine, diff dose/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Nerve damage
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 13.03.2023
- 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: nein
Extra dose administered
Symptomtext
No ADR Nurse gave dose to the wrong resident. This resident had already received a bivalent booster dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 06.03.2023
- Impfdatum
- 09.02.2023
- Beginn
- 09.02.2023
- 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
Bivalent was given as first dose in series instead of primary. No adverse signs or symptoms reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 03.03.2023
- Impfdatum
- 05.12.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 1,0
- Dosis
- 5
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Cerebrovascular disorder
Confusional state
Fall
Head injury
Intraventricular haemorrhage
Subarachnoid haemorrhage
Symptomtext
on 12/6/22, rt noted to have confusion, and was complaining of being weak and having no energy, early morning of 12/7/22 rt was found on floor in bathroom, he was sent to hospital, with subarachnoid hemorrhage where he hit his head, also found to have multiple brain bleeds (intraventricular hemorrhages, and extensive microvasculopathy,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hx CVA, type 2 diabetes, CKD, hypothyroidism, essential hypertension, GERD, osteoarthritis, COPD, gout,
- Andere Medikamente
- Culturelle, levothyroxine, loratidine, omeprazole, amlodipine, Lipitor, citalopram, Colace, folic acid, insulin detemir
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 05.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
Covid 19; Covid 19; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 43-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 05Oct2022 as dose 4 (booster), single (Lot number: GJ6739) at the age of 43 years for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2023, outcome "unknown" and all described as "Covid 19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) positive; (22Feb2023) positive, notes: Tested positive again. Therapeutic measures were taken as a result of drug ineffective, covid-19 included paxlovid from 14Feb2023 to 18Feb2023. 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; Test Result: Positive ; Test Date: 20230222; Test Name: Covid-19 test; Test Result: Positive ; Comments: Tested positive again
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 28.12.2022
- Beginn
- 28.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
PATIENT RECEIVED PFIZER BIVALENT VACCINE ON 12/28/22 BUT HAD ALREADY RECEIVED A BIVALENT DOSE ON 11/1/22 FROM ANOTHER PHARMACY. IT WAS NOT REPORTED ON IMMPRINT BY THE OTHER PHARMACY PROVIDER UNTIL 12/26/22, WHICH WAS AFTER IMMPRINT WAS CHECKED TO APPROVE THE DOSE ON 12/28.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 26.02.2023
- Impfdatum
- 31.01.2023
- Beginn
- 31.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Upon revieweing the expiration date for Phizer-Biontech covid 19 vaccine, bivalent (NDC 59267-0304-02), find out that pharmacist was accidentally gave expired vaccine to patient. Lot #GJ6739 extended expiration date 1/31/24. Date took out from Cooler (@-90 to -60C) was 11/21/22. Beyond use date (@2 to 8C) was 1/31/23 (10 weeks or 70th day). Date given to patient was 1/31/23 (71st day). Reached out Pfizer Manufacturer for guidance for information about vaccine stability. According to Pfizer medical information, recommended/labeled storage time in the prescribing information and excursion time. Vaccine was stable for total time of 72 hours = (10 weeks or 70 days labeled time plus 2 days excursion time) at temperature of 2 - 8 C. Unable to reach out patient at this time but left voicemail.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 25.02.2023
- Impfdatum
- 15.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 6,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Atrial fibrillation
Symptomtext
AFib events lasting about 36 hours occurring at 5 day intervals
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- -
- Andere Medikamente
- Metoprolol Eliquis Lipitor
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 26.09.2022
- Beginn
- 01.02.2023
- Tage bis Beginn
- 128,0
- Dosis
- 5
- Route/Site
- - / -
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) (Physician). A 77-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 26Sep2022 as dose 5 (booster), single (Lot number: GJ6739) at the age of 76 years for covid-19 immunisation; BNT162b2 (BNT162B2), on 01Apr2022 as dose 4 (booster), single (Lot number: FJ9943) for covid-19 immunisation; BNT162b2 (BNT162B2), on 28Jan2021 as dose 1, single (Lot number: EN9581), on 17Feb2021 as dose 2, single (Lot number: EL9266) and on 28Sep2021 as dose 3 (booster), single (Lot number: 30155BA) for covid-19 immunisation. The patient's relevant medical history included: "HTN" (unspecified if ongoing), notes: HTN; "High Cholesterol" (unspecified if ongoing); "Known allergies: Sulfa" (unspecified if ongoing), notes: Known allergies: Sulfa. The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset Feb2023, latency 1 year 11 months 29 days 20 hrs 30 min after the suspect product(s) administration, outcome "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19 with Paxlovid from 06Feb2023 to 11Feb2023.; Sender's Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the events (VACCINATION FAILURE, COVID 19) and BNT162B2.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: High cholesterol; Hypertension (HTN); Sulfonamide allergy (Known allergies: Sulfa)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 20.09.2022
- Beginn
- 01.02.2023
- Tage bis Beginn
- 134,0
- Dosis
- 5
- Route/Site
- - / RA
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) from product quality group. The reporter is the patient. A 57-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 20Sep2022 as dose 5 (booster), single (Lot number: gj6739) at the age of 56 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), 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. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Feb2023, outcome "unknown" and all described as "Treatment of COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (Feb2023) Positive, notes: Positive test result following Paxlovid treatment. Therapeutic measures were taken as a result of drug ineffective, covid-19 with paxlovid treatment start date: 04Feb2023 to 08Feb2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202302; Test Name: Test; Test Result: Positive ; Comments: Positive test result following Paxlovid treatment.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 20.02.2023
- Impfdatum
- 17.11.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 45,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy
Lichen sclerosus
Symptomtext
I had my vaccination on 11/17/2022. I had a routine wellness examination on 01/23/2023. I was diagnosed with Lichen sclerosus on 01/30/2023. I was prescribed two different steroids. I do have a follow up scheduled for 03/06/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy
- Hospital-Tage
- -
- Labordaten
- Biopsy 02/13/2023
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Penicillin
- Vorherige Impfungen
- COVID-19; Infection at injection site with first vaccination
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 19.02.2023
- Impfdatum
- 01.11.2022
- Beginn
- 23.11.2022
- Tage bis Beginn
- 22,0
- Dosis
- 5
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Biopsy bone marrow normal
Blood test normal
Computerised tomogram normal
Immune thrombocytopenia
Magnetic resonance imaging abdominal normal
Platelet count decreased
Splenomegaly
Symptomtext
I routinely get my blood tested for other reasons. It was normal on my last test in September. On 11/23/22, my platelet count had plummeted, and I have since then been undergoing followup tests and treatment for ITP. Also, enlarged spleen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy bone marrow normal
- Hospital-Tage
- 3,0
- Labordaten
- Referring you to Dr., my hematologist. Numerous blood tests, CT (December) and MRI (January) of abdomen; bone marrow biopsy (December or January). All negative to date. Platelet deficiency treated initially with steroids (dexymethosone, then prednisone), followed by Doptelet.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High blood pressure, thyroid conditions,
- Andere Medikamente
- Labetalol; levothyroxine, simivistatin, potassium citrate, Flonase, loratadine
- Allergien
- Pennicilin; amoxicyllin; sulfa; allergic contact dermatitis (chemicals, plastics, synthetics)
- Vorherige Impfungen
- Chills and fever lasting one day. 63. 4/25/22. Pfizer, fourth shot.
- Staat
- AZ
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 16.02.2023
- Impfdatum
- 10.12.2022
- Beginn
- 04.12.2021
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Interchange of vaccine products
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; Vaccine brand=Pfizer / BioNTech; vaccine dose number=2/ vaccine brand other= Moderna; vaccine dose number=3; 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 60-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 10Dec2022 at 14:30 as dose 5 (booster), single (Lot number: GJ6739) at the age of 59 years, in right arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 08Jan2021 at 10:15 as dose 1, single (Lot number: EH9899), in right arm and on 29Jan2021 at 14:45 as dose 2, single (Lot number: EL1283), in right arm for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), on 04Dec2021 at 09:00 as dose 3 (booster), single (Lot number: 033H21A), in right arm and on 14May2022 at 14:00 as dose 4 (booster), single (Lot number: 001M21A), in right arm for covid-19 immunisation. The patient's relevant medical history included: "need thyroid medication" (unspecified if ongoing), notes: other medical history: need thyroid medication. Concomitant medication(s) included: LEVOTHYROXINE, start date: Nov1995. The following information was reported: INTERCHANGE OF VACCINE PRODUCTS (medically significant) with onset 04Dec2021 at 09:00, outcome "unknown", described as "Vaccine brand=Pfizer / BioNTech; vaccine dose number=2/ vaccine brand other= Moderna; vaccine dose number=3"; 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: Positive, notes: 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
- Test Name: COVID 19 Test; Test Result: Positive ; Comments: COVID 19 Treatment
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Thyroid disorder (other medical history: need thyroid medication)
- Andere Medikamente
- LEVOTHYROXINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 15.02.2023
- Impfdatum
- 15.02.2023
- Beginn
- 15.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
no negative effects
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 14.02.2023
- Impfdatum
- 24.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19; COVID 19; 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 51-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 24Oct2022 at 12:00 as dose number unknown (booster), single (Lot number: GJ6739) at the age of 50 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose number unknown, 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), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19". Therapeutic measures were taken as a result of drug ineffective, covid-19 included Paxlovid from 31Jan2023 to 05Feb2023. 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
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 13.02.2023
- Impfdatum
- 13.02.2023
- Beginn
- 13.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
patient denied any symptoms. will continue to monitor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 13.02.2023
- Impfdatum
- 27.11.2022
- Beginn
- 01.02.2023
- Tage bis Beginn
- 66,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose
Glucose tolerance impaired
Glycosylated haemoglobin normal
Symptomtext
I went to the doctor for my check-up. I had routine blood work to check A1C and fasting blood sugar. My A1C jumped from 5.5 to 5.9. This was all in one year. The doctor suggested lifestyle changes to bring the numbers down. I have never had issues with my A1C in my past, until this vaccine. I am now diagnosed with Pre-Diabetes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood glucose
- Hospital-Tage
- -
- Labordaten
- 01FEB2023- Blood Panel - High A1C
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Seasonal Allergies; Asthma
- Andere Medikamente
- Singular; Levocetirizine; Fluticasone; Atenolol; Azelastine Hydrochloride; Biotin Collagen; Corsi tine Bromalin; Magnesium; Hyaluronic Acid; Digital Blue; Turmeric, Vitamin C, Co Quetin
- Allergien
- Shellfish; Seafood; Penicillin; Cetric cline; Cetaphil; Secor; Iodine; Sulfa Drugs
- Vorherige Impfungen
- I was given the very first dose after just getting over COVID-19. I started itching all over. I was monitored and the itching di
- Staat
- MN
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 09.02.2023
- Impfdatum
- 06.12.2022
- Beginn
- 06.12.2022
- 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 events. Patients received bivalent vaccine as first dose instead of the monovalent vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 59,0
- Geschlecht
- U
- Eingang
- 06.02.2023
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- 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
Symptomtext
Community outreach completed at local Nursing Home. Consents signed by Nursing Home administrators/guardians for patient to receive vaccine. Health Center staff thought nursing home had record of primary dose series of covid vaccine that was not entered to show me vax. Bivalent dose given as error that now, per CDC recommendations will serve as the "1st dose" and vaccine series will be completed correctly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- unknown, patient is a nursing home resident
- Vorgeschichte
- unknown, patient is a nursing home resident
- Andere Medikamente
- unknown patient is a nursing home resident
- Allergien
- unknown patient is a nursing home resident
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 60,0
- Geschlecht
- U
- Eingang
- 06.02.2023
- Impfdatum
- 17.11.2022
- Beginn
- 17.11.2022
- 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
Community outreach completed at Nursing Home. Consents signed by Nursing Home administrators/guardians for patient to receive vaccine. Health Center staff thought nursing home had record of primary dose series of covid vaccine that was not entered to show me vax. Bivalent dose given as error that now, per CDC recommendations will serve as the "1st dose" and vaccine series will be completed correctly
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown, patient resident of nursing home
- Vorgeschichte
- unknown, patient resident of nursing home
- Andere Medikamente
- unknown, patient resident of nursing home
- Allergien
- unknown, patient resident of nursing home
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 03.02.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- 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
Bivalent given instead of monovalent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- F
- Eingang
- 03.02.2023
- Impfdatum
- 06.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. An 80-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 06Oct2022 as dose 4 (booster), single (Lot number: GJ6739), 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 had no relevant medical history. 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 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient received Paxlovid for COVID 19 treatment from 13Jan2023 to 17Jan2023. Patient had no known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 02.02.2023
- Impfdatum
- 02.02.2023
- Beginn
- 02.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Health Dept. participated in off site clinic at Care Center . Client presented to receive covid 19 bivalent booster vaccine. According to client consent form, client's current covid-19 vaccination card, and record in state immunization database, client is eligible for bivalent booster shot today. Bivalent booster shot administered as planned by RN. Client then states her current last name is not the name she has on her consent form or her covid-19 vaccination card. Client looked up in state database under other last name to find out that she had already in fact received bivalent booster and was not eligible today. Client monitored for extra 15 minutes after vaccination. No s/s distress noted. Client informed to let staff at care center know if she was not feeling well and client verbalized understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 01.02.2023
- Impfdatum
- 01.11.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 30,0
- Dosis
- 5
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Paranasal sinus hypersecretion
Respiratory tract congestion
Rhinorrhoea
Sinus disorder
Sinusitis
Symptomtext
I had a sinus Infection that has been going on forever. Since mid-December I have had constant sinus problems. I did not have before this 5th shot. I often feel congestion. I have runny nose drainage. I have a cough and just overall sinusitis. I contacted my Teladoc and was given antibiotics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Blood Pressure; High Cholesterol; Sleep Apnea
- Andere Medikamente
- Declined
- Allergien
- Tetracycline
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 30.01.2023
- Impfdatum
- 27.10.2022
- Beginn
- 15.01.2023
- Tage bis Beginn
- 80,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Aphonia
Cough
Deafness
Paranasal sinus discomfort
SARS-CoV-2 test negative
Sinusitis
Tympanic membrane perforation
Viral infection
Symptomtext
I had my vaccination on 10/27/2022. On 01/15/2023 I got a viral infection which brought coughing, loss of voice and sinus pressure. I was diagnosed with Sinusitis on 01/18/2023. I loss my hearing on 01/22/2023. I saw my NP on 01/28/2023 with ear drops as I had a ruptured ear drop. I tested COVID-19 Negative on 01/28/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aphonia
- Hospital-Tage
- -
- Labordaten
- 01/28/2023 COVID-19 Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Spironolactone
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 29.01.2023
- Impfdatum
- 24.01.2023
- Beginn
- 24.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 29.01.2023
- Impfdatum
- 24.01.2023
- Beginn
- 24.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 26.01.2023
- Impfdatum
- 21.09.2022
- Beginn
- 16.11.2022
- Tage bis Beginn
- 56,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Hypersomnia
Positive airway pressure therapy
Respiratory failure
SARS-CoV-2 test positive
Symptomtext
Patient brought to the ED by EMS for evaluation of excessive sleepiness on 11/16/22. His living facility became concerned when he could not stay awake that day. COVID-19 PCR test was done which resulted positive. Ultimately, patient admitted 11/16/22 for further management of respiratory failure likely related to COVID-19 infection as well as chronic conditions of OSA (on CPAP) and morbid obesity. He was placed on BiPAP initially, however oxygen needs improved during his hospitalization. He was able to be weaned down to his baseline supplemental oxygen need of 2L. Patient improved and was discharged 11/21/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 25.01.2023
- Impfdatum
- 09.01.2023
- Beginn
- 09.01.2023
- 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
Incorrect vaccine administered. Patient had never received any COVID-19 vaccinations, but was given the Bivalent COVID-19 booster vaccine. No treatment needed. CDC recommendations for COVID-19 administration errors were followed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 25.01.2023
- Impfdatum
- 05.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Dysphonia
Throat irritation
Symptomtext
tickle in throat, coughing, hoarsness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- provastatin,penicillin, ciproflaxin, percodein
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 20.01.2023
- Beginn
- 20.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product contamination
Symptomtext
Patient vaccinated with Pfizer Bivalent Booster vial that was considered contaminated. Vial was considered contaminated because it was previously punctured with a used needle. Used/contaminated needle was from vaccine given to affected patient's wife.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product contamination
- Hospital-Tage
- -
- Labordaten
- Lab work to R/O blood borne pathogens recommended and offered to patient, but patient declined.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 24.01.2023
- Impfdatum
- 29.10.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 23,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Swelling face
Transient ischaemic attack
Symptomtext
TIA, swollen face
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Swelling face
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Prabastain, slizess
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
FACILITY ADMINISTERED BIVALENT VACCINE FOR A 2ND DOSE INSTEAD OF THE MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 27.12.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
FACILITY ADMINISTERED BIVALENT VACCINE FOR A 1ST DOSE INSTEAD OF THE MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 19.01.2023
- Beginn
- 19.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incomplete course of vaccination
Incorrect product formulation administered
Symptomtext
Client received one dose of Pfizer vaccine on 1/14/2023. RN discussed restarted the vaccine series since the client never received her 2nd dose of the series. The client agreed to restart the series however the RN administered the bivalent vaccine instead of the monovalent vaccine. She immediately called me to report this error. The client was informed of the vaccine she received by the nurse soon after vaccine administration. I consulted with Dr., the Mobile team Medical Director. Dr. advised that no additional vaccine were needed for this client, since she received the bivalent vaccine. A call was made on 1/19/23 with the site contact, (client), Mobile Team Program Director, and myself (NP). All questions and concerns were addressed with the client.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incomplete course of vaccination
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 19.01.2023
- Beginn
- 19.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
Booster dose given after receiving a bivalent dose on 11/21/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 20.01.2023
- Impfdatum
- 20.01.2023
- Beginn
- 20.01.2023
- 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
No adverse event
Symptomtext
Patient received a second bivalent booster after receiving their first on 9/16/2022. No adverse events occurred.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 20.01.2023
- Impfdatum
- 20.01.2023
- Beginn
- 20.01.2023
- 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
Patient received a second bivalent booster after receiving their first on 9/16/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 20.01.2023
- Impfdatum
- 06.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Vaccination failure
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter (Other HCP). The reporter is the patient. A 40-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 06Oct2022 as dose 4 (booster), single (Lot number: GJ6739) at the age of 40 years, in left arm for covid-19 immunisation; BNT162b2 (BNT162B2), on 06Apr2021 as dose 1, single (Lot number: EW0150), in left arm, on 27Apr2021 as dose 2, single (Lot number: EW0171), in left arm and on 31Oct2021 as dose 3 (booster), single (Lot number: FF2593), in left arm for covid-19 immunisation. The patient's relevant medical history included: "Prediabetic" (unspecified if ongoing); "IBS" (unspecified if ongoing); "POCS" (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 "unknown" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: the patient was treated with Paxlovid. I tested negative for covid two day after finishing Paxlovid but then tested postitive six days after finishing Paxlovid.; Sender's Comments: Based on the available information in the case, the causal association between the events VACCINATION FAILURE, COVID-19 and the suspect drug BNT162B2 cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Irritable bowel syndrome; Polycystic ovarian syndrome; Prediabetes
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 17.01.2023
- Impfdatum
- 04.01.2023
- Beginn
- 04.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
PT GIVEN 2 DOSES OF PFIZER BIVALENT VACCINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 17.01.2023
- Impfdatum
- 30.11.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alanine aminotransferase increased
Aspartate aminotransferase increased
Autoimmune hepatitis
Blood alkaline phosphatase increased
Computerised tomogram abdomen abnormal
Gamma-glutamyltransferase increased
Hepatic steatosis
Laboratory test abnormal
Liver function test increased
Scan with contrast abnormal
Smooth muscle antibody positive
Symptomtext
Patient had been evaluated by me for RUQ pain and elevated LFTs since around Oct2022. Initially thought to be related to heavy alcohol use, she discontinued use. We then discontinued crestor and zetia. At this point she received her immunization with the bivalent covid booster. Then we checked several more labs, LFTs continued to rise and positive autoimmune markers suggesting autoimmune hepatitis. She was then referred to hepatology. Repeat LFTs now down trending a bit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Alanine aminotransferase increased
- Hospital-Tage
- -
- Labordaten
- 17Oct2022: AST 65, ALT 110 05Dec2022: GGT 149, AST 85, ALT 145, Alk Phos 129, Actin Smooth Muscle Ab 44 29Dec2022: AST 50, ALT 73 11Jan2023: ALT 77, Alk Phos 128 02Nov2022 CT Abd/Pelvis with and without oral and IV contrast : demonstrate mod/severe fatty infiltration, microlobulated margins, possible cirrhosis. Unremarkable gallbladder and bile ducts
- Aktuelle Erkrankungen
- Right upper quadrant pain, elevated AST, elevated ALT,
- Vorgeschichte
- Moderate persistent asthma, impaired fasting glucose, hyperlipidemia, obesity, hypertension, depression, arthritis, allergic rhinitis, plantar fasciitis
- Andere Medikamente
- .HCTZ 25mg orally daily .Valsartan 160mg orally daily .Advair 250/50 inhaler twice daily .Xopenex HFA 45mcg - 2 puffs every 4-6 hours as needed for shortness of breath .Zyrtec 10mg orally daily .Metformin 500mg orally twice daily .Omepraz
- Allergien
- Prednisone
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 15.01.2023
- Impfdatum
- 12.01.2023
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient attended an immunization clinic hosted by pharmacy. Because I was not at the event, I am unsure if patient had a previous covid card. When attempting to bill the vaccine at the store the next day, a rejection came up showing plan limitations exceeded. Patient already received the bilavent Pfizer vaccine on 9/11/22, which means a second bivalent booster was administered at this clinic. Patient is not answering the phone to check in, but a message was left. The event was reported in our internal reporting system.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 14.01.2023
- Impfdatum
- 03.11.2022
- Beginn
- 22.12.2022
- Tage bis Beginn
- 49,0
- 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
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 65-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 03Nov2022 as dose 5 (booster), single (Lot number: Gj6739) at the age of 65 years, in left arm for covid-19 immunization; BNT162b2 (BNT162B2), on 18Mar2021 as dose 1, single (Lot number: Ep7534), in left arm, on 06Apr2021 as dose 2, single (Lot number: Er8732), in left arm, on 13Oct2021 as dose 3 (booster), single (Lot number: Ff2593), in left arm and on 10May2022 as dose 4 (booster), single (Lot number: Fm9992), in left arm for covid-19 immunization. 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 22Dec2022, outcome "recovered with sequelae" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (22Dec2022) Positive; (31Dec2022) Negative; (07Jan2023) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient tested positive for COVID on 22Dec2022. The patient started 5 day course of Paxlovid. Completed Paxlovid course as directed on 28Dec2022. Symptoms resolved and tested negative on 31Dec2022. Rebound COVID symptoms begin to reappear on 05Jan2023. Symptoms continued to get worse and tested positive for COVID again on 07Jan2023. Treated COVID symptoms with OTC cold flu medicine and slept 18 hours per day. The patient was beginning to feel much better on 11Jan2023.The patient had no known allergies.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221222; Test Name: COVID-19 test; Test Result: Positive ; Test Date: 20221231; Test Name: COVID-19 test; Test Result: Negative ; Test Date: 20230107; Test Name: COVID-19 test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: known allergies No other medical history No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 13.01.2023
- Impfdatum
- 13.01.2023
- Beginn
- 13.01.2023
- 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
No adverse event
Symptomtext
Patient stated it was his 3rd dose of the pfizer vaccine when it was actually his 6th dose. So far after talking to him he had no side affects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None applicable
- Aktuelle Erkrankungen
- None Known
- Vorgeschichte
- Diabetes
- Andere Medikamente
- None Known
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 13.01.2023
- Impfdatum
- 13.10.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 25,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Atrial fibrillation
Cardiac monitoring abnormal
Symptomtext
I received the Pfizer Bivalent COVID-19 booster on 10/13/2022. On 11/7/2022, I arrived at an outpatient surgical hospital to undergo hip replacement surgery. When I was hooked up to the heart monitor prior to getting an IV, the monitor indicated that I had atrial fibrillation. I had never had this problem before or any other cardiac issues. The surgery was immediately canceled, and I was told to go to an emergency room. When I got to the ER, another reading was done of my heart. I was still experiencing atrial fibrillation 12 hours after it was first detected. The ER doctor prescribed me a blood thinner, Eliquis, to prevent a stroke. I was then discharged and advised to see a cardiologist within a couple of days. Unfortunately, I was unable to see a cardiologist right away. On or about 11/10/2022, I saw my PCP, and he did not detect atrial fibrillation at that point. He did tell me, though, that I should see a cardiologist for further diagnosis. I saw a cardiologist on or about 11/16/2022. When the cardiologist examined me, I was in atrial fibrillation. I was diagnosed with periodic atrial fibrillation. It is intermittent, and since I have learned to detected it with a smart watch, I monitored my situation daily. The longest I have experienced atrial fibrillation since learning to monitor the condition has been 30 hours; the shortest duration was 21 hours. I can then go for up to a week with normal cardiac rhythm. At the time of this writing, I have gone for 2 full weeks at normal rhythm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anticoagulant therapy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Osteoarthritis.
- Andere Medikamente
- Vitamin D3; Motrin (As Needed).
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 03.10.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
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 62-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 03Oct2022 as dose 5 (booster), single (Lot number: gj6739) at the age of 61 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 had no relevant medical history. There were no concomitant medications, also reported as no other medication in 2 weeks. Patient had no known allergies. 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; (Jan2023) Positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Patient received COVID-19 Treatment with Paxlovid (Lot number: gf6426) from 01Jan2023 to 02Jan2023. The noxious taste that the Paxlovid created in mouth was untenable and unbearable for patient. After three doses patient had to stop. However it was now day 14 and she was still testing positive and still have symptoms and wonder if that's because she only took three doses of Paxlovid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid test; Test Result: Positive ; Test Date: 202301; Test Name: Covid test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 13.10.2022
- Beginn
- 04.01.2023
- Tage bis Beginn
- 83,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Delivery
Exposure during pregnancy
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough case all Pfizer dose 1 3/10/21 EL9267 dose 2 3/31/21 ER8727 dose 3 12/16/21 33130BA vaginal delivery on 1/4/23, 39.3 wga
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ 12/30/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 13.01.2023
- Impfdatum
- 13.10.2022
- Beginn
- 04.01.2023
- Tage bis Beginn
- 83,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Delivery
Exposure during pregnancy
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
covid vaccine breakthrough case all Pfizer dose 1 3/10/21 EL9267 dose 2 3/31/21 ER8727 dose 3 12/16/21 33130BA vaginal delivery on 1/4/23, 39.3 wga
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- covid+ 12/30/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 05.10.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 65,0
- Dosis
- 5
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Magnetic resonance imaging
Magnetic resonance imaging spinal
Sciatica
Symptomtext
Sciatica in left leg.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Magnetic resonance imaging
- Hospital-Tage
- -
- Labordaten
- MRI of back and hip
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetic; high blood pressure
- Andere Medikamente
- REBETRON; lisinopril; famotidine; lovastatin; B12; calcium; multivitamin
- Allergien
- Vancomycin
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 10,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 09.01.2023
- Beginn
- 09.01.2023
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
patient received bivalent booster for 12 and older
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 13.12.2022
- Beginn
- 13.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
No adverse event
Symptomtext
The patient did not have an adverse event from this vaccine. He should have received the first dose of the Pfizer Covid 19 vaccine series. This would have been his first dose. We were doing both vaccines in the clinic and the nurse gave him the Bivalent as his first dose in error. We wanted to report this event. Thank you
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none noted on form
- Vorgeschichte
- None noted on form
- Andere Medikamente
- N/A
- Allergien
- No known allergies - Pt did not have a negative outcome after receiving the medication. He should have received the primary series before the bivalent vaccine since this was his first Covid vaccine.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- IL
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 08.10.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
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
- -
- Staat
- NY
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- VA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 29.09.2022
- 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
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 68-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 29Sep2022 as dose 5 (booster), single (Lot number: GJ6739) at the age of 68 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; desvenlafaxine succinate monohydrate (PRISTIQ), (Batch/Lot number: unknown); fexofenadine hydrochloride (ALLEGRA [FEXOFENADINE HYDROCHLORIDE]), (Batch/Lot number: unknown); fluticasone propionate (FLONASE [FLUTICASONE PROPIONATE]), (Batch/Lot number: unknown); buspirone (BUSPIRONE), (Batch/Lot number: unknown); naproxen (NAPROXEN), (Batch/Lot number: unknown). The patient's relevant medical history included: "Cardiac arrhythmia" (unspecified if ongoing); "allergic rhinitis" (unspecified if ongoing); "Depression with anxiety" (unspecified if ongoing); "Depression with anxiety" (unspecified if ongoing); "perennial allergies" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), outcome "unknown", COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: The patient had no known allergies. She received Paxlovid for COVID-19 treatment, started from 25Dec2022 to 29Dec2022.; Sender's Comments: As per the available information the causality of the events drug ineffective, covid-19 with the suspect can not be ruled out completely.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergic rhinitis; Anxiety; Cardiac arrhythmia; Depression; Perennial allergy
- Andere Medikamente
- PRISTIQ; ALLEGRA; FLONASE; BUSPIRONE; NAPROXEN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 22.09.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- 70,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
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 37-year-old female patient (not pregnant) received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 22Sep2022 as dose 4 (booster), single (Lot number: GJ6739) at the age of 37 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 and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Dec2022, outcome "unknown" and all described as "COVID-19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Negative. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: Other medication in 2weeks was reported as yes. Patient received Paxlovid treatment from 28Dec2022 to 01Jan2023 for Covid-19, other medication in 2 weeks product Levothyroxine 25 mcg, other medication in 2 weeks product: nifedipine, other medication in 2 weeks start date: 04Dec2021, other medication in 2 weeks stop date: 27Dec2022, other medication in 2 weeks product lisinopril, other medication in 2 weeks start date: 29Dec2022. Paxlovid/COVID Rebound 5 days after testing negative and symptoms had gone away. The sore throat returned. adverse event start date: 05Jan2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 20.10.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 22,0
- Dosis
- 5
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Prostatic specific antigen
Prostatic specific antigen increased
Symptomtext
PSA levels have gone up and gotten high enough for need to biopsy his prostate for cancer/PSA level rose to 9.24; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from medical information team, Program. The reporter is the patient. A 67-year-old male patient received BNT162b2, BNT162b2 omi ba.4-5 (BNT162B2, BNT162B2 OMI BA.4-5), on 20Oct2022 as dose 5 (booster), 0.3 ml single (Lot number: GJ6739) at the age of 67 years intramuscular, in left deltoid for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. Vaccination history included: BNT162b2 (Dose 01, Anatomical Site of injection: Left deltoid , Route of Administration: intramuscular. , Batch/Lot number: EL8982), administration date: 03Feb2021, when the patient was 65-year-old, for COVID-19 Immunization; BNT162b2 (dose 02, Anatomical Site of injection: Left deltoid , Route of Administration: intramuscular , Batch/Lot number: EN6201), administration date: 24Feb2021, when the patient was 65-year-old, for COVID-19 Immunization; BNT162b2 (Dose: 03, Batch number: EWW015, Dosage text: .3ml intramuscular once left deltoid, Indication as Reported by the Primary Source: media recommending that a booster was available and it made sense if had initial two to get it), administration date: 27Sep2021, when the patient was 66-year-old, for COVID-19 Immunization, reaction(s): "Mentioned that his levels increased to 6.16 after the first booster that was administered on 27Sep2021"; BNT162b2 (Dose: 04, Batch/lot number : FK9893, Dosage text: .3ml intramuscular once left deltoid, Indication as Reported by the Primary Source: indicated that the booster was available everybody encouraging get the booster when it came out), administration date: 18Apr2022, when the patient was 67-year-old, for COVID-19 Immunization. The following information was reported: PROSTATIC SPECIFIC ANTIGEN INCREASED (non-serious) with onset 11Nov2022, outcome "unknown", described as "PSA levels have gone up and gotten high enough for need to biopsy his prostate for cancer/PSA level rose to 9.24". The events "psa levels have gone up and gotten high enough for need to biopsy his prostate for cancer/psa level rose to 9.24" required physician office visit. Relevant laboratory tests and procedures are available in the appropriate section. Additional information: The caller reported that he had received five Pfizer COVID-19 vaccines. Two of them were the two initial ones and three COVID-19 boosters and the last one was on 20Oct2022. Seemed the last booster was the Bivalent and was going to get a biopsy done at a hospital because his PSA levels have gone up. Past three times it was at least 4 and the second to last time it increased to 6 something and on 11Nov2022 it got up to 9.24. Because it was trending up, they want to do a biopsy to see if it was prostate cancer. Caller stated that his PSA levels had gradually gone up before he got the fourth vaccine. Had his first COVID vaccine in Feb2021 and the levels had gone up prior to that but not above the acceptable level. Acceptable level was 4.0. Later clarified that the levels had exceeded acceptable level in Aug2019 before he had the vaccines. Wanted to mention the two PSA levels prior to his first Pfizer COVID 19 vaccine that they were done in 2019 and one was 3.86 and 4.39 there was a trending increase that started before the first COVID booster. Later clarified that he has only had two PSA levels since he started the COVID 19 vaccinations. Provided that the PSA acronym was for the prostate specific antigen. There was no doctor that prescribed these. Got them on his own. PSA levels have gone up to 6.16. Mentioned that his levels increased to 6.16 after the first booster that was administered on 27Sep2021. Had the first PSA level done on 27Dec2021 and that level 6.16. Mentioned that there was a PSA done since then on 11Nov2022 and it rose to 9.24. Stated that he did not recover from it because it went up to 9.24. Just monitored it no treatment. PSA level rose to 9.24: Does not know whether it has gone up, stayed the same or gone down. Clarified later in the report that the outcome as unknown. Treatment: Urologist wanted to do prostate biopsy to see if prostate cancer was present. The prior vaccinations within 4 weeks were reported as none. Caller was going to the hospital next month to have a biopsy done and he was asking if the last booster shot which was the bivalent will give him adequate protection. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Prostatic specific antigen
- Hospital-Tage
- -
- Labordaten
- Test Name: PSA; Result Unstructured Data: Test Result:4.0 or a tad bit higher; Comments: The past 3 times, his PSA levels have started trending up so the urologist wants to do a biopsy. First time it was 4.0 or a tad bit higher At least 4; Test Name: PSA; Result Unstructured Data: Test Result:6 point something; Comments: Second to last one done, PSA increased to 6 point something second to last time it increased to 6 something; Test Date: 2019; Test Name: PSA; Result Unstructured Data: Test Result:3.86; Test Date: 2019; Test Name: PSA; Result Unstructured Data: Test Result:4.39; Test Date: 201908; Test Name: PSA; Result Unstructured Data: Test Result:exceeded level 4.0; Comments: Acceptable level is 4.0. Later clarified that the levels had exceeded acceptable level in Aug 2019 before he had the vaccines; Test Date: 20211227; Test Name: PSA; Result Unstructured Data: Test Result:6.16; Comments: Had the first PSA level done on 27Dec2021 and that level 6.16; Test Date: 20221111; Test Name: PSA; Result Unstructured Data: Test Result:9.24; Comments: Mentioned that there was a PSA done since then on 11Nov2022 and it rose to 9.24
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Family Medical History Relevant to Adverse Events (AEs): None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- CT
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- OH
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- OH
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- MA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 13.10.2022
- Beginn
- 13.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- IL
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 13.10.2022
- Beginn
- 13.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 13.10.2022
- Beginn
- 13.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- GA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- 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: nein
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
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- PA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- TX
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 09.10.2022
- Beginn
- 09.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- MA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
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
- -
- Staat
- NY
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -
- Staat
- NY
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- -