- Staat
- MI
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 13.04.2023
- Impfdatum
- 18.10.2022
- Beginn
- 10.03.2023
- Tage bis Beginn
- 143,0
- Dosis
- N/A
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
COVID-19
Cardiac septal hypertrophy
Computerised tomogram thorax abnormal
Condition aggravated
Dysphagia
Echocardiogram abnormal
Ejection fraction
Hepatic steatosis
Hypersomnia
Hypertransaminasaemia
Hyporesponsive to stimuli
Hypotension
Hypoxia
Laboratory test abnormal
Lactic acidosis
Leukocytosis
Mental status changes
Symptomtext
Discharge Provider: MD Primary Care Provider: DO Admission Date: 3/10/2023 Discharge Date: Mar 23, 2023 PRESENTING PROBLEM: Sepsis (HCC) Severe sepsis (HCC) Septic shock (HCC) HOSPITAL COURSE: 83 y.o. who has a past medical history significant for CKD, schizophrenia, bipolar disorder, previous CVA with residual weakness who presented on 3/10 with an acute onset of altered mentation, fever, hypoxemia and hypotension. Per family, she is slow to respond to questions at baseline and sleeps up to 20 hours per day. CT chest showed bilateral multifocal pneumonia. Labs were significant for AKI, mild lactic acidosis, transaminitis, elevated troponins and leukocytosis. UA with mild pyuria. She was given 4L IV fluids then started on vasopressors due to persistent hypotension. US of RUQ c/w fatty liver. Echo showed moderate concentric hypertrophy with assymetric severe septal hypertrophy (1.5 cm). No LV outflow obstruction at time of study. LVEF 66%. 1 of 2 blood cultures (+) for coag neg Staph - contaminant Zosyn deescalated to Augmentin and completed 7 day course. In addition to pneumonia, found to be COVID+, She was started on remdesivir to complete 5 days with CMP monitoring. Decadron 6 mg daily for 10 days. Patient's acute kidney injury had resolved. For her hypertrophic cardiomyopathy cardiology consulted and recommended non urgent outpatient visit in the next 1-2 months for re-evaluation and consideration of further testing such as cardiac MRI for her prior history of amyloidosis. PTOT evaluation recommended skilled nursing facility placement. Doctor consulted and recommended dysphagia diet and outpatient ENT follow up. Psychiatry consulted and did deem patient mentally compensated and appropriate and no need for inpatient psychiatry.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Septic shock
- Hospital-Tage
- 13,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Dysphagia Pneumonia Right bundle branch block (RBBB) History of nicotine dependence Depression Schizophrenia (HCC) Essential hypertension Dyslipidemia Schizoaffective disorder, bipolar type (HCC) Reactive airway disease Transient cerebral ischemia Other amyloidosis (HCC) Stage 3a chronic kidney disease (HCC) Transaminitis Scalp lesion Hypertrophic cardiomyopathy (HCC) Pyuria
- Andere Medikamente
- acetaminophen (TYLENOL) 325 MG tablet aluminum, magnesium & simethicone (MAALOX EX) 400-400-40 MG/5ML aspirin EC 81 MG enteric coated tablet atorvastatin (LIPITOR) 80 MG tablet cholecalciferol (VITAMIN D3) 25 MCG (1000 UT) tablet isosorbide
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 23.09.2022
- Beginn
- 26.09.2022
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Guillain-Barre syndrome
Immunoglobulin therapy
Symptomtext
Contracted Guillain-Barre Syndrome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- 14,0
- Labordaten
- Full dosages of Immunoglobulin Therapy
- Aktuelle Erkrankungen
- not ill at the time of the vaccination.
- Vorgeschichte
- mild emphysema
- Andere Medikamente
- atorvastatin, OTC Magnesium, Zinc spray, Vit. D3, Vit. B12
- Allergien
- only allergic to Bupropion
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 16.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Condition aggravated
Dizziness
Nausea
Parosmia
Seizure
Symptomtext
Patient had a small seizure within 24 hours after the vaccine was administered. She has had seizures in the past. Symptoms included dizziness, nausea, & chemical smell. These are same symptoms during her seizures.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 23.03.2023
- Impfdatum
- 28.02.2023
- Beginn
- 01.03.2023
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
Malaise
Pyrexia
Rash
SARS-CoV-2 test positive
Symptomtext
patient reported having fever, malaise, difficulty breathing, and a rash on her left arm for several days after the vaccination date. she did not go seek any healthcare and symptoms resolved on their own.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- she tested positive on at-home covid tests for 2 days
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- copd
- Andere Medikamente
- pramipexole, ventoin, spironolactone lisinopril, bupropion, buspirone
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 07.02.2023
- Impfdatum
- 12.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Atrial fibrillation
Barium double contrast
Chronic obstructive pulmonary disease
Computerised tomogram
Computerised tomogram abdomen
Constipation
Cystoscopy
Dry mouth
Dyspnoea
Faeces soft
Magnetic resonance imaging
Muscular weakness
Pollakiuria
Sleep disorder
Ultrasound abdomen
Ultrasound kidney
Urodynamics measurement
Symptomtext
Frequency of urination: 40-50 times a day: still ongoing, but less frequent--12-15 times a day Severe constipation: lasting over 2-1/2 months; still ongoing with bloated stomach; liquid and very soft stool (unformed) owing to multiple laxatives Muscle weakness in thigh and calf; still ongoing Atrial fibrillation Extremely dry mouth--still ongoing, particularly at night COPD; breathing issues, particularly at night and mostly while lying down; less so sitting or standing up or during the day Waking up every 45 minutes to an hour at night due to dry mouth, unable to breathe, or a desperate urge to urinate
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Don't recall dates, but most tests were done October, November, and December 2022. They include CT scans of GI tracts, esophagus, stomach; MRI of prostrate; Barium contrast tests; Cystoscopy; Urodynamics. Had an ultrasound of kidney and bowels on2/7/23.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Crestor; Losartan; Metformin; Zetia; Cosopt; Zioptan; Vitamin D-3; CoQ10; Vitamin B-12
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- 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: nein
Burning sensation
Chest pain
Injection site erythema
Injection site pain
Injection site pruritus
Rash pruritic
Symptomtext
Site: Itching at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Systemic: patient expierenced a redness, rash that burned and itched all the way around her arm and was about 3 inches wide. patinet also complained of have chest pains-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 23.05.2023
- Impfdatum
- 14.12.2022
- Beginn
- 14.12.2022
- 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 pain
X-ray limb
Symptomtext
Patient reports pain at injection site that started a few hours after receiving vaccine. He presumed it was normal soreness from the vaccine but the pain did not improve. The pain has worsened over time. He has intermittent sharp stabbing pain at the injection site that was occurring weekly but it is now occurring daily.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- x-ray right shoulder 5/23/23
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- hypertension, hyperlipidemia
- Andere Medikamente
- Losartan 100 mg daily Rosuvastatin 10 mg daily Sertraline 50 mg daily Zyrtec 10 mg daily
- Allergien
- Bacitracin-Neomycin-Polymyxin ointment neomycin sulfate tabs neosporin ointment
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 17.01.2023
- Impfdatum
- 21.09.2022
- Beginn
- 21.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
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
- MO
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 12.11.2022
- Impfdatum
- 10.11.2022
- Beginn
- 11.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Injection site warmth
Symptomtext
Patient called pharmacy to report that she woke up in the early morning of 11/11 with the arm she got pneumovax in having swollen to twice its normal size and being red and warm to the touch. She took acetaminophen for it, which had little effect. She debated calling in sick to work but chose to go in anyway. Patient called the pharmacy in the afternoon on 11/11 to report this reaction and say that while it hasn't yet gone down, it hasn't gotten any worse either. Advised patient to try benadryl and topical hydrocortisone over the counter and monitor; if worsens to visit urgent care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- Fosamax, Metoprolol tartarate, levothyroxin, atorvastatin, lisinopril, clopidogrel, esomeprazole, potassium chloride
- Allergien
- codeine
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 01.11.2022
- Beginn
- 02.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Insomnia
Symptomtext
Shoulder pain unrelieved by OTC pain relievers and difficulty sleeping due to pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 31.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal discomfort
Abdominal distension
Abdominal pain upper
Diarrhoea
Flatulence
Symptomtext
Starting the day of the immunizations, pt had stomach cramps, gas, and bloating. After about a week, she begun having diarrhea. She got her immunizations on 10/11/2022 and is still having stomach upset as of 10/31/22. She has tried to treat with immodium and pepto bismol. She is planning on following up with her doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain upper
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 19.10.2022
- Impfdatum
- 15.10.2022
- Beginn
- 15.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye swelling
Pruritus
Swelling face
Urticaria
Symptomtext
Pt received vaccine at approximately 4:50pm, however later that night she started to experience swelling of the eyes and face, and she also developed hives over most of her body with itchiness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Nausea
Symptomtext
patient stated that she felt nauseated and dizzy for 2 days...
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none known
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- none known
- Allergien
- no known allergies to medications, food, or other products...
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 09.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inflammation
Injection site erythema
Local reaction
Pruritus
Symptomtext
redness below injection site roughly 3 inches to 8 inches below. Red, itching, inflamed. Localized reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 15.09.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Vaccination site pain
Vaccination site swelling
Symptomtext
Developed swelling about 4 inches further down in their inner arm; Tenderness about 4 inches further down and in their inner arm; This spontaneous case was reported by a nurse and describes the occurrence of VACCINATION SITE SWELLING (Developed swelling about 4 inches further down in their inner arm) and VACCINATION SITE PAIN (Tenderness about 4 inches further down and in their inner arm) in a 70-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. AS7144B) for COVID-19 prophylaxis. Co-suspect product included non-company product INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE HIGH DOSE QUADRIVALENT) for an unknown indication. Concurrent medical conditions included Hypertension. Concomitant products included LOSARTAN for Hypertension. On 15-Sep-2022, the patient received dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form and dose of INFLUENZA VACCINE INACT SPLIT 4V (FLUZONE HIGH DOSE QUADRIVALENT) (unknown route) 1 dosage form. On 15-Sep-2022, the patient experienced VACCINATION SITE SWELLING (Developed swelling about 4 inches further down in their inner arm) and VACCINATION SITE PAIN (Tenderness about 4 inches further down and in their inner arm). The patient was treated with NAPROXEN SODIUM (ALEVE) at an unspecified dose and frequency. At the time of the report, VACCINATION SITE SWELLING (Developed swelling about 4 inches further down in their inner arm) and VACCINATION SITE PAIN (Tenderness about 4 inches further down and in their inner arm) had resolved. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter did not provide any causality assessments. The patient had a location reaction to one of the vaccines. The patient had received Flu shot: Fluzone Highdose along with Moderna COVID bivalent on 15-Sep-2022 on the upper left arm. Then not right away but later that day she developed swelling and tenderness about 4 inches further down and in their inner arm. Patient mentioned that it did go away. Patient took Aleve after the reaction and it helped.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hypertension
- Vorgeschichte
- -
- Andere Medikamente
- LOSARTAN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 04.10.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain in extremity
Peripheral swelling
Skin warm
Symptomtext
patients rt arm became swollen, red, hot, and painful Tues night after getting the fluzone HD. Symptoms did not subside by Wed night so patient was seen and prescribed keflex
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 04.10.2022
- Impfdatum
- 29.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site erythema
Injection site warmth
Symptomtext
Site: Redness at Injection Site-Medium, Additional Details: redness over whole upper arm and wrappingaround to back, warm to touch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 27.09.2022
- Impfdatum
- 23.09.2022
- Beginn
- 23.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Dizziness
Headache
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Headache-Mild, Additional Details: anxiety attack
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 26.09.2022
- Impfdatum
- 20.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 2,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site rash
Injection site warmth
Symptomtext
Site: Redness at Injection Site-Mild, Systemic: Allergic: Rash (specify: facial area, extremeties)-Mild, Additional Details: redness, rash on arm localized to right deltoid area, warm to touch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 10.09.2022
- Impfdatum
- 10.09.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Symptomtext
Patient states that her hands and bottoms of her feet are itching
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Cilostazol 50mg, Rosuvastatin 5mg
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.10.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Medication error
No adverse event
Product administered to patient of inappropriate age
Symptomtext
administered the HIGH DOSE to patients under 65 with no adverse event; Initial information received on 18-Oct-2022 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves an unknown age/gender patient who experienced administered the high dose to patients under 65 with no adverse event while receiving vaccine INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE (lot UJ904AD; expiry date: 30-Jun-2023) in unknown administration site for immunization. On an unknown date the patient developed a non-serious event administered the high dose to patients under 65 with no adverse event (product administered to patient of inappropriate age) (unknown latency) following the administration of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE. Action taken: not applicable. At time of reporting, the outcome was Unknown for the event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 19.10.2022
- Impfdatum
- 19.10.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
duplicate shot, received 1 week prior
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient was given 2 doses of fluzone HD quad vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- .
- Aktuelle Erkrankungen
- .
- Vorgeschichte
- .
- Andere Medikamente
- .
- Allergien
- .
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient was given 2 doses of fluzone HD quad vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- .
- Aktuelle Erkrankungen
- .
- Vorgeschichte
- .
- Andere Medikamente
- .
- Allergien
- .
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 12.10.2022
- Impfdatum
- 12.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- COVID
- Vorgeschichte
- ARTHRITIS, HYPERTENSION, KIDNEY DISEASE
- Andere Medikamente
- AMOLIDIPINE, ASPRIN-81, ATORVASTATIN, PLAVIX, DICLOFENAC SODIUM 1%, ESCITALOPRAM, GRALISE, HYDROCHLOROTHIAZIDE, NORTRIPTYLINE, POTASSIUM, SODIUM BICARBONATE, TURMERIC, VITAMIN D
- Allergien
- BACTRIM, SULFA, FLOMAX, CYMBLATA, IV CONTRAST DYE, BETA ADRENERGIC BLOCKERS, ISONIAZID
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 04.10.2022
- Impfdatum
- 04.10.2022
- Beginn
- 04.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Symptomtext
Patient called later stating that about 30 minutes after receiving the vaccines, she was in the store rest room and felt very weak. Husband took her to the hospital. She was there waiting to see a doctor. She will update us if they find anything. Husband received same vaccines with no problem. She had Moderna before and now Pfizer so she suspected that she might be allergic to Pfizer or since she had 3 vaccines at the same time, it might be too much.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- Patient was still waiting to see a doctor.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 25.09.2022
- Impfdatum
- 24.09.2022
- Beginn
- 24.09.2022
- 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
Patient requested flu and covid vaccines. He received both and his wife ( not present) called and said he was not supposed to get a flu shot and that he already had one last week. He received 2 flu shots. She stated he is mixing things up. He had no problems with flu shot he already had
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Wife stated he did fine with the first flu shot
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 23.09.2022
- Beginn
- 23.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
COVID vaccine administered was the Pfizer Pediatric COVID vaccine instead of the Pfizer Bivalent Booster vaccine. Pt has been advised to come back and receive the correct vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 23.09.2022
- Impfdatum
- 23.09.2022
- Beginn
- 23.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Pt was given the Fluzone HD for 65 year old and above patients, but was not yet 65 years old. Pt did not feel any side effects or adverse reactions but was counseled on risk of getting higher dose of flu vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 16.09.2022
- Impfdatum
- 16.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient received Fluzone HD and is < 65 yoa.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Fluzone HD was given to a patient who was 51 years old
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NDKA
- Vorherige Impfungen
- -