- Staat
- MI
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 20.05.2022
- Impfdatum
- 06.11.2021
- Beginn
- 12.05.2022
- Tage bis Beginn
- 187,0
- Dosis
- N/A
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute respiratory failure
Blood creatinine increased
COVID-19
Creatinine renal clearance decreased
Pancytopenia
White blood cell count decreased
Symptomtext
Admission Date: 5/12/2022 Discharge Date: 5/14/2022 HOSPITAL PROBLEMS 1. AHRF secondary to Covid-19 infection 2. CKD3b 3. Pancytopenia 4. OSA 5. CAD s/p CABG 6. COPD 7. Gout 8. Barretts esophagus HOSPITAL COURSE: Patient is a 91 y.o. male who was admitted to hospital with AHRF secondary to Covid-19 infection. AHRF/Covid-19 infection: Patient required 2L NC on admission to maintain saturations. Was started on 10 day course of decadron. Did not start Remdesivir due to low CrCl. Patient improved quickly, and was weaned to room air. Observed for 24hrs to ensure no further desaturations. None noted so patient discharged home to finish course of Decadron. CKD3b: Cr mildly increased from baseline at 1.92. Remained around this level throughout admission. Pancytopenia: Patient has know anemia secondary to CKD, as well as thrombocytopenia. WCC also noted to be decreased. Likely overall pancytopenia secondary to Covid-19 infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- History of Barrett's esophagus Dyslipidemia Anemia due to stage 3b chronic kidney disease (HCC) Idiopathic chronic gout of multiple sites without tophus Primary insomnia Moderate COPD (chronic obstructive pulmonary disease) (HCC) Hx of asbestos exposure Mycobacterium avium complex (HCC) History of bladder cancer Nocturnal hypoxemia CAD s/p CABG x 4 in 1999 without angina pectoris Stage 3b chronic kidney disease (HCC) OSA on CPAP Lung nodule Thrombocytopenia (HCC) Chronic fatigue
- Andere Medikamente
- allopurinol (ZYLOPRIM) 100 MG tablet aspirin 325 MG tablet atorvastatin (LIPITOR) 20 MG tablet Calcium Carbonate-Vitamin D (CALCIUM + D PO) dexamethasone (DECADRON) 6 MG tablet fish oil-omega-3 fatty acids 1000 MG capsule LORazepam (A
- Allergien
- Lipitor [Hmg-coa-r Inhibitors]Myalgia MorphineOther NiacinGout Nitrates, Organic [Organic Nitrates]Headache
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 30.10.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Symptomtext
Patient passed out in store about 1 hour after his vaccines. Patient was assessed by EMS and it was determined patient had only eaten noodles a few hours before vaccines and was light-headed due to not having eating in combination with vaccines. Patient left with parents on his own accord.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 25.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Loss of consciousness
Symptomtext
PATIENT PASSED OUT ABOUT 10 MINUTES AFTER RECEIVING VACCINATIONS. WITHIN A MINUTE OR SO SHE WAS UP AND DRINKING WATER. REFUSED CARE FROM 911 STATED THAT SHE HAD NOT EATEN, HAD NO PROBLEM WITH FIRST 2 DOSES OF PFIZER COVID19 VACCINE. PATIENT WAS MONITORED FOR ANOTHER 15 MINUTES BEFORE LEAVING. SAID SHE WAS FEELING MUCH BETTER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 01.09.2021
- Impfdatum
- 28.08.2021
- Beginn
- 28.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Syncope
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 19.08.2021
- Impfdatum
- 19.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
PT DEVELOPED SYNCOPE AFTER GETTING HER FLU SHOT. PT WAS PLACED ON THE FLOOR AND FEET WERE ELEVATED. EMS CALLED. PT GOT BETTER AND REFUSED EMS. PT LEFT ON HER OWN WITH HER HUSBAND.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- UNDER ACTIVE THYROID
- Andere Medikamente
- SYNTHROID 75MCG, VITAMIN D OTC
- Allergien
- NA
- Vorherige Impfungen
- FLU SHOT 3 YEARS AGO
- Staat
- MI
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 04.11.2021
- Beginn
- 29.09.2022
- Tage bis Beginn
- 329,0
- Dosis
- N/A
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aortic valve incompetence
Brain natriuretic peptide increased
COVID-19
Cardiac failure acute
Cardiac failure congestive
Chest X-ray abnormal
Condition aggravated
Cough
Dyspnoea
Echocardiogram abnormal
Hypoxia
Left ventricular failure
Lung infiltration
Mitral valve incompetence
Polyuria
SARS-CoV-2 test positive
Symptomtext
Discharge Provider: Primary Care Provider: Admission Date: 9/29/2022 Discharge Date: Oct 1, 2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute on chronic combined systolic and diastolic CHF (congestive heart failure) (HCC) [I50.43] COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 75 year old female with PMHx of chronic systolic CHF, HTN, CKD3, CAD, A-fib who presented to the hospital with shortness of breath and cough. She was found to be COVID-19 positive in the ER and had hypoxia. Patient had a CXR showing bilateral infiltrates. However the patient also had a significantly elevated BNP and was given IV lasix along with remdesivir and decadron. Patient improved quickly and was able to be weaned to room air off her O2. Patient diuresed well. She was afebrile after admission. Given her quick improvement (and symptoms only a few days) decadron was stopped as COVID-19 pneumonia was unlikely. Patient was kept and given 3 days of IV remdesivir. Patient was feeling much better at the time of discharge, she was breathing well on room air with no shortness of breath or cough, no fever. Patient was then considered stable for discharge home. Patient was instructed on signs and symptoms of when to return to the ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN (hypertension), benign Edema extremities Hypothyroidism due to acquired atrophy of thyroid Glaucoma Sensorineural hearing loss Macular degeneration, wet (HCC) Breast mass, right At risk for injury from chemotherapy History of radiation exposure Non-ischemic cardiomyopathy, EF 35% s/p CRT-D (chemo vs other) Atrial fibrillation (HCC) Acute on chronic combined systolic and diastolic heart failure (HCC) History of breast cancer GERD (gastroesophageal reflux disease) Enlarged lymph node, subcarinal seen on CT, 14 mm Pulmonary nodules Nausea Mood insomnia (HCC) Advance care planning Atrial flutter (HCC) Atrial flutter/AF with rapid ventricular response (HCC) Complete heart block (HCC) MR (mitral regurgitation), mild/mod Echo 6/2022 Nonrheumatic aortic valve insufficiency, mild/mod Echo 6/2022 Coronary artery disease involving native coronary artery of native heart without angina pectoris Biventricular implantable cardioverter-defibrillator (ICD) in situ Chronic combined systolic and diastolic heart failure (HCC) Pneumonia due to COVID-19 virus Acute respiratory failure with hypoxia (HCC)
- Andere Medikamente
- amiodarone (PACERONE) 200 MG tablet apixaban (ELIQUIS) 5 MG tablet aspirin 81 MG chewable tablet atorvastatin (LIPITOR) 40 MG tablet calcium-vitamin D (CALCIUM 600+D) 600-200 MG-UNIT TABS per tablet dapagliflozin (FARXIGA) 10 MG TABS tablet
- Allergien
- ThimerosalSwelling Ceclor [Cefaclor]Hives Arimidex [Anastrozole]Other Brinzolamide Dye-contrastHives Netarsudil Shellfish Allergy
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 16.08.2022
- Impfdatum
- 06.10.2021
- Beginn
- 13.08.2022
- Tage bis Beginn
- 311,0
- Dosis
- N/A
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood potassium decreased
COVID-19
Condition aggravated
Diarrhoea
Hypokalaemia
Laboratory test
Nausea
Palpitations
SARS-CoV-2 test positive
Vomiting
Symptomtext
Discharge Provider: Private MD Primary Care Provider at Discharge: Private MD Admission Date: 8/13/2022 Discharge Date: 8/13/2022 DETAILS OF HOSPITAL STAY: HOSPITAL COURSE: Patient is a 65 y.o. female who presented to local Hospital as a transfer from ED for hypokalemia. Patient initially presented to emergency department for nausea, vomiting, diarrhea, and palpitations. Symptoms began 08/09/2022, and she took a home COVID test which was positive on 08/11/2022. Patient has history of low potassium and experiencing palpitations. In the emergency department she was found to have hypokalemia at 2.8, and intractable nausea. She was given potassium replacement, Zofran, IV fluids and sent to hospital for observation. On the general floor, patient had full resolution of nausea, vomiting, and diarrhea. She tolerated normal breakfast without difficulty. She did not have return of palpitations and repeat lab work showed resolution of hypokalemia. Patient was considered medically and vitally stable for discharge home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Tendonitis of wrist, right Elevated lipase Dehydration Osteoarthritis of right knee History of abdominoplasty Aspiration pneumonia of lower lobe, unspecified aspiration pneumonia type, unspecified laterality (HCC)
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet amLODIPine (NORVASC) 5 MG tablet escitalopram (LEXAPRO) 10 MG tablet hydroCHLOROthiazide (HYDRODIURIL) 25 MG tablet levothyroxine (SYNTHROID) 50 MCG tablet ondansetron (ZOFRAN) 4 MG tablet potassium chl
- Allergien
- Vesicare [Solifenacin] Nitrofurantoin MacrocrystalHives
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 23.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Extra dose administered
Neuralgia
Paraesthesia
Symptomtext
Patient states she has been experiencing significant neuropathic pain in unilateral left arm after receiving Pfizer vaccine. Pain is described as burning and tingling extending from site of vaccination at the deltoid to the tips of the fingers on the left arm. Pain was not present for this patient prior to receiving 3rd dose booster vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Consultation with specialist (neurologist)
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Multiple sclerosis
- Andere Medikamente
- duloxetine 30mg, lisinopril/hctz 20-12.5mg, baclofen 20mg, oxybutynin ER 5mg, pramipexole 0.125mg, gabapentin 300mg, diazepam 5mg, myrbetriq ER 25mg, kesimpta (specialty)
- Allergien
- No known drug allergies
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 26.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Chills
Fatigue
Headache
Pyrexia
Symptomtext
Patient experienced a severe chest tightness a day after providing the vaccinations. Patient describe it as she was able to breathe but the tightness was very painful as she though twice about calling emergency number. She got headache, feverish and chills. She felt tired/exhausted and lasted for 4 days after the providing the vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/a
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 17.02.2023
- Impfdatum
- 12.10.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Magnetic resonance imaging
Symptomtext
Patient reports right should pain starting after the 2021 influenza vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Patient has MRI
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
reddness, pain and swelling at injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- received antibiotics
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.07.2022
- Impfdatum
- 23.09.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 21,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Post-traumatic stress disorder
Symptomtext
3 weeks after vaccination developed bilateral achy hip pain. She did not present to healthcare provider at that time. She had trouble walking due to pain. Slowly resolved over the course of 2 months
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No known illnesses at time of vaccination or one month prior
- Vorgeschichte
- Sleep Apnea, IBS, Borderline Personality Disorder, PTSD
- Andere Medikamente
- None
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Headache
Nausea
Pyrexia
Vomiting
Symptomtext
Thirty minutes after receiving vaccine, associate became nauseous and had a headache. She progressed to vomiting and fever of 102. This continued for several days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
PATIENT COMPLAINING OF PAIN IN THE ARM NOT GOING AWAY EVEN WITH MEDICATION 10 DAYS LATER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 18.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure increased
Erythema
Head discomfort
Malaise
Vision blurred
Symptomtext
PATIENT WAS GIVEN HER FLU VACCINE IN HER LEFT ARM AT 2PM. A FEW MINUTES LATER SHE CALLED ME AND TOLD ME SHE WASN'T FEELING WELL. HER NECK AND SCALP BECAME RED. EYES WERE BLURRY. SHE FELT LIKE, "HER HEAD WAS GOING TO EXPLODE". BLOOD PRESSURE BECAME ELEVATED FROM HER NORMAL BP. CALLED 911. SHE STARTED TO FEEL BETTER BEFORE 911 CAME. SHE WENT TO GET CHECKED OUT AT HOSPITAL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 4,0
- Geschlecht
- F
- Eingang
- 15.10.2021
- Impfdatum
- 15.10.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Swelling face
Symptomtext
Patient woke this morning with left sided facial swelling and rash under her arms and groin area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 24.09.2021
- Impfdatum
- 21.09.2021
- Beginn
- 21.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pruritus
Rash erythematous
Symptomtext
RED RASH WITH ITCHING ON FACE (EAR, EYE, NOSE), THROAT/NECK, CHEST, B/L ARMS AND LEGS. NO WEEPING/OPEN SORES, NOT PAINFUL JUST ITCHY. NO SHORTNESS OF BREATH. PT STATES ONSET ABOUT 1HR AFTER ADMINISTRATION OF VACCINE WITH SYMPTOMS SPREADING/WORSENING EACH DAY. PT SOUGHT MEDICAL ATTENTION AND RECEIVED PRESCRIPTION FOR PREDNISONE 9/24/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- PT SOUGHT MEDICAL ATTENTION AND RECEIVED PRESCRIPTION FOR PREDNISONE 9/24/21
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 23.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Flushing
Urticaria
Symptomtext
several hours post vaccine patient is experiencing hives on the trunk of her body and redness and flushing of her face. Her temperature at home was 99.6 degrees but when we rechecked it was 98.6 here at the pharmacy at the time she was lodging her complaint
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- had severe reaction to Prevnar in her youth
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 20.10.2021
- Impfdatum
- 05.10.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
Patient received a Pfizer Covid booster. Their first 2 vaccines were Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 0,2
- Geschlecht
- F
- Eingang
- 19.10.2021
- Impfdatum
- 15.10.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
Patient was given Fluarix instead of Pediarix at the time of the event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 15.10.2021
- Impfdatum
- 04.10.2021
- Beginn
- 04.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental exposure to product
Accidental underdose
Needle issue
Syringe issue
Underdose
Symptomtext
Underdose due to vaccine leakage; dose dripped over the patients arm; Inadvertent exposure to vaccine; This case was reported by a nurseand described the occurrence of accidental underdose in a 39-year-old female patient who received Flu Seasonal QIV Dresden (Fluarix Quadrivalent 2021-2022 season) (batch number 34yn4, expiry date 30th June 2022) for prophylaxis. Co-suspect products included flu seasonal qiv dresden pre-filled syringe device (Fluarix Tetra Pre-Filled Syringe Device) injection syringe for prophylaxis. On 4th October 2021, the patient received Fluarix Quadrivalent 2021-2022 season and Fluarix Tetra Pre-Filled Syringe Device. On 4th October 2021, unknown after receiving Fluarix Quadrivalent 2021-2022 season and Fluarix Tetra Pre-Filled Syringe Device, the patient experienced accidental underdose, exposure via skin contact and inadvertent exposure to vaccine. On an unknown date, the outcome of the accidental underdose, exposure via skin contact and inadvertent exposure to vaccine were unknown. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional details provided as follows: Nurse reported that the patient received underdose of the vaccine due to vaccine leakage, which led to accidental underdose. The reporter claimed that the needle was not properly attached to the prefilled syringe. They were not sure how much of the vaccine was administrated but claimed most of the dose dripped to the floor and the patients arm, which led to exposure via skin contact and inadvertent exposure to vaccine. No further events were reported. The reporter consent to follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental exposure to product
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 04.10.2021
- Impfdatum
- 17.09.2021
- Beginn
- 17.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administration error
Symptomtext
There wasn't actually an adverse event but I didn't see an option for a form for an administration error. We had only processed one of his 2 shots through the computer system so at first it seemed like he had gotten an extra vaccine. However we discovered he had wanted both vaccines and we just hadn't processed the flu shot through the computer. I am sorry if this isn't something that needs to be reported to you but my boss asked me to.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administration error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No listed illnesses.
- Vorgeschichte
- No listed chronic or long-standing health conditions.
- Andere Medikamente
- No listed medications.
- Allergien
- No listed allergies.
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 03.10.2021
- Beginn
- 03.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
Patient received the influenza vaccine instead of the COVID vaccine. No adverse events were documented.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 04.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
No adverse event
Symptomtext
Sub-therapeutic dose: Patient should of received a High Dose Varriation. No adverse event reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/a
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- 30.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injury associated with device
Symptomtext
Vaccination was successful. Immediately afterwards I engaged the needle guard. The guard did not cover the tip of the needle and I jabbed my thumb.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injury associated with device
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 21.09.2021
- Impfdatum
- 18.09.2021
- Beginn
- 18.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Patient received the fluarix rather than the age recommended fluad.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None.
- Andere Medikamente
- Unknown.
- Allergien
- NKDA
- Vorherige Impfungen
- -