- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 24.03.2023
- Impfdatum
- 26.10.2022
- Beginn
- 07.03.2023
- Tage bis Beginn
- 132,0
- Dosis
- N/A
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute respiratory failure
Atelectasis
Bradycardia
Bronchial secretion retention
COVID-19
Chest X-ray abnormal
Computerised tomogram thorax abnormal
Cough
Decreased appetite
Dyspnoea
Haemoglobin decreased
Lung consolidation
Oropharyngeal pain
Pneumonitis
Procalcitonin normal
SARS-CoV-2 test positive
Symptomtext
Discharge Provider: MD Primary Care Provider: MD Admission Date: 3/7/2023 Discharge Date: Mar 10, 2023 PRESENTING PROBLEM: Hypoxia [R09.02] Acute respiratory failure with hypoxia COVID-19 HOSPITAL COURSE: Patient is a 73 y.o. male with a past medical history of essential tremor, chronic back pain with implanted morphine pump, non insulin-dependent type 2 diabetes and depression who presents today with cough, dyspnea and anorexia. Symptoms started on 02/27. The patient states that it started with a sore throat and cough. In the ER the patient was noted to be hypoxic on room air with an SpO2 of 87%. He remained hypoxic on nasal cannula and required non-rebreather with 15 L of oxygen. He did receive an albuterol inhaler and 6 mg of Decadron. He was able to be weaned down to 6 L by nasal cannula. His other vital signs were unremarkable. Labs significant for hemoglobin 12.7. Procalcitonin was negative. Viral PCR positive for COVID-19. Chest x-ray with new mild left basilar atelectasis or pneumonitis. CTA thorax showed mucous plugging w consolidation. Pt was started on remdsivir and decadron. 02 req improved and after 48 hrs was on 3L. On the 3rd day he was able to be weaned off 02. Labs and VS stable throughout stay. Did become bradycardic in the 30's, believe it was due to remdesivir and this was discontinued. Stable for discharge on 3/10. Discharged with decadron to finish 10 day course.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Non-toxic multinodular goiter Hashimoto's disease End of battery life of intrathecal infusion pump Chronic pain Diabetes mellitus Tobacco dependence Disabling essential tremor Depression COVID-19
- Andere Medikamente
- Calcium Carb-Cholecalciferol 600-200 MG-UNIT TABS Cholecalciferol 1000 units CAPS clonazepam (KLONOPIN) 1 MG tablet docusate (COLACE) 100 MG capsule EPINEPHrine (EPIPEN) 0.3 MG/0.3ML escitalopram (LEXAPRO) 20 MG tablet metFORMIN (GLUCOPHAGE
- Allergien
- Shellfish AllergyHives LatexItching Topamax [Topiramate]Hives TrazodoneHives
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 15.11.2022
- Impfdatum
- 26.09.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 5,0
- Dosis
- UNK
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Balance disorder
Gait inability
Guillain-Barre syndrome
Lumbar puncture abnormal
Mobility decreased
Lumbar puncture
Magnetic resonance imaging
Vaccination site pain
Motor dysfunction
Muscular weakness
Neck pain
Neuralgia
Pain
Pain in extremity
Symptomtext
guillain barre syndrome; prolonged injection site pain, sharp, shooting pain in both arms; Initial information received on 04-Nov-2022 regarding an unsolicited valid serious case received via consumer/non-hcp (doctor daughter) and doctor. This case involves a 72-year-old male patient who experienced Guillain barre syndrome and prolonged injection site pain, sharp, shooting pain in both arms after receiving vaccines Moderna COVID-19 vaccine and 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. This case is linked to case 2022SA462123(same reporter). On 26-Sep-2022, the patient received suspect Fluzone High-Dose Quadrivalent vaccine at dose 0.7 ml once (lot: UJ875AA) via unknown route in the right arm for immunization. On 26-Sep-2022, the patient received a booster dose of suspect MODERNA COVID-19 VACCINE not produced by at (unknown: formulation, strength, dose, lot number not reported via unknown route) in the left arm for immunization. On unknown date in Oct-2022, at 2 weeks latency after vaccination of Fluzone High-Dose Quadrivalent vaccine and MODERNA COVID-19 VACCINE, the patient developed a non-serious prolonged injection site pain described as sharp, shooting pain in both arms (vaccination site pain). The patient was hospitalized on 16-Oct-2022. On 17-Oct-2022 the patient was diagnosed with a serious Guillain barre syndrome (Guillain-Barre syndrome) both at 22 days latency following the administration of Fluzone High-Dose Quadrivalent vaccine and MODERNA COVID-19 VACCINE. This event was assessed as medically significant. The patient was already hospitalized when the event occurred and still in the hospital. Action taken: Fluzone High-Dose Quadrivalent and MODERNA COVID-19 VACCINE was not applicable. It was not reported if the patient received a corrective treatment for the events. At time of reporting, the outcome was Not Recovered for both events.; Sender's Comments: company comment 14-Oct-2022: This case involves a 72-year-old male patient who experienced Guillain barre syndrome and prolonged injection site pain, sharp, shooting pain in both arms after vaccination with Fluzone High-Dose Quadrivalent. Furthermore, information regarding condition at the time of vaccination, role of medical history, concomitants, lab data excluding other predisposing etiologies would be needed for complete assessment of the case. The role of co-suspect Moderna COVID-19 vaccine could be confounder in case. Based upon the reported information, the role of an individual vaccine cannot be assessed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Guillain-Barre syndrome
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 10.11.2022
- Impfdatum
- 03.11.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Seizure
Symptomtext
Patient came into the pharmacy today to state that he received a flu shot from our pharmacy last Thursday (11/3/22). He stated that he had a seizure the night of 11/4/22 and that the flu shot is the only change in his life (in his 78 years). His doctor informed him to come to the pharmacy so we could file a report. Patient received Fluzone High Dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- allergy to penicillin is the only medical history we have on file.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 05.06.2023
- Impfdatum
- 26.09.2022
- Beginn
- 13.05.2023
- Tage bis Beginn
- 229,0
- Dosis
- N/A
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Akinesia
Anticoagulant therapy
Asthenia
Atrial flutter
COVID-19
Cardioversion
Chest X-ray normal
Echocardiogram
Echocardiogram abnormal
Ejection fraction decreased
Fall
Gait inability
Laboratory test normal
SARS-CoV-2 test positive
Supraventricular tachycardia
Symptomtext
5/13/2023 - 5/19/2023 (6 days) DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Generalized weakness Fall, initial encounter COVID-19 virus infection COVID-19 HOSPITAL COURSE: Patient is a 70 y.o. male with a PMHx of DM type II, Depression, GERD and hx of gastric ulcers who presented to the ED due to weakness. In the ED, vitals signs and labs were stable. CXR without acute process. Resp film array resulted positive for COVID-19. He was unable to ambulate in ED therefore requested admission for placement. On admission he remained stable from a respiratory standpoint. During admission he was noted to have SVT. This was not corrected with vagal maneuvers or adenosine. Cardiology was consulted and patient underwent TEE with cardioversion. Suspected underlying rhythm was aflutter with RVR. Eliquis was started. He was also noted to have reduced ejection fraction during procedure so limited echo was repeated before discharge. Limited echo showing EF 40% with akinesis. Cardiology recommended a repeat limited echo in 1 month, 2 week Ziopatch and he was continued on Eliquis. He was seen by PT/OT who recommended home with home health and therapies. He was discharged in medically stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Supraventricular tachycardia
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type 2 diabetes mellitus with neurologic complication, with long-term current use of insulin Essential hypertension GERD (gastroesophageal reflux disease) Depression Obesity Hyperlipidemia History of esophageal stricture with dilatation Blepharospasm syndrome Ulnar impingement syndrome, left Esophageal stricture Esophagitis Normocytic anemia CAD (coronary artery disease) Peripheral vascular disease, unspecified COVID-19
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet albuterol (PROVENTIL, VENTOLIN, PROAIR) 108 (90 Base) MCG/ACT inhaler apixaban (ELIQUIS) 5 MG tablet atorvastatin (LIPITOR) 40 mg tablet B-D UF III MINI PEN NEEDLES DULoxetine (CYMBALTA) 60 MG delayed
- Allergien
- Oxycontin [Oxycodone]Swelling, Rash
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 24.01.2023
- Impfdatum
- 18.10.2022
- Beginn
- 16.01.2023
- Tage bis Beginn
- 90,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Back pain
Blood creatinine increased
Blood culture
COVID-19
Chest X-ray normal
Computerised tomogram head normal
Cough
Fall
Fatigue
Head injury
Laboratory test
Mobility decreased
Pyrexia
SARS-CoV-2 test positive
Spinal X-ray normal
White blood cell count increased
Symptomtext
Discharge Provider: DO Primary Care Provider: MD Admission Date: 1/16/2023 Discharge Date: Jan 19, 2023 COVID positive date: 1/16/2023 PRESENTING PROBLEM: COVID-19 [U07.1] HOSPITAL COURSE: Patient is a 82 y.o. female with past medical history of hypertension, hyperlipidemia, Parkinson's disease, non-insulin-dependent diabetes with peripheral neuropathy, CKD 3 and benign essential tremor, presented to ED due to generalized weakness and inability to get out of her recliner. She sustained a fall hitting her head and was unable to get up. EMS was summoned and she declined to present to ED. Spent day resting in her recliner and when she attempted to get up was unable to, so EMS was again summoned and brought her to ED. She reported 2-3 days of nonproductive cough, had fever per EMS. Patient has chronic fatigue. Patient reported intermittent weakness due to Parkinson's disease but was able to get around in her house with help of walker. Patient has fallen twice in past 6 months per her husband. Patient has chronic back pain which is unchanged from baseline. Patient also noted lower extremity swelling which is chronic and unchanged. In ED she was febrile to 38.5. Remainder of VSS on RA. Labs with creatinine 1.11, WBC 11.74, LA 1.0. COVID+. Blood cultures were drawn. CT head and CXR unremarkable. She was given 500ml IVF and Tylenol. Patient was admitted with generalized weakness secondary to COVID19. Patient started complaining of acute back pain. X-rays of the spine were done which showed no acute abnormalities. Patient was given 1 time dose of IV Dilaudid which resulted in hallucinations. IV Dilaudid was discontinued and patient was given oral oxycodone for better pain control. Patient was also given Flexeril and provided with heat packs. Physical therapy and occupational therapy were consulted and recommended patient return home with home health care. Pt. will continue with her home tramadol and lidocaine patches for her back pain. Pt. to follow up with her PCP outpatient. She is discharging in improved and stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension associated with diabetes Morbid obesity with BMI of 40.0-44.9, adult Gastroesophageal reflux disease without esophagitis Constipation, unspecified constipation type Type 2 diabetes mellitus with diabetic neuropathy, without long-term current use of insulin Peripheral neuropathy Chronic pain of left knee Parkinsonism, unspecified Parkinsonism type OAB (overactive bladder) Detrusor instability of bladder Stage 3a chronic kidney disease Hyperlipidemia associated with type 2 diabetes mellitus Hypothyroidism (acquired) Primary insomnia Generalized weakness Mild depression, active, no psychosis GAD (generalized anxiety disorder) Rotator cuff tear Abnormal EKG Urinary incontinence without sensory awareness Difficulty walking Abnormality of gait Physical deconditioning Tremor
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet ALPRAZolam (XANAX) 0.25 MG tablet amLODIPine (NORVASC) 5 MG tablet carbidopa-levodopa (SINEMET) 25-100 MG per tablet escitalopram (LEXAPRO) 20 MG tablet ezetimibe (ZETIA) 10 MG tablet glipiZIDE (GLUCOTR
- Allergien
- Lincomycin [Lincomycin] Neurontin [Gabapentin] Zithromax [Azithromycin] Levaquin Metformin Vesicare [Solifenacin Ciprofloxacin Clarithromycin Clindamycin Sulfadiazine Sulfamethoxazole W-trimethoprim Trimethoprim Cefaclor Pravastatin Simvastatin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 12.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Hypertension
Symptomtext
Systemic: Hypertension-Mild, Additional Details: patient had acute hypertension 90 minutes after vaccine. not sure if related but wanted to report. went to er and they gave her meds to calm and bring down bp. only lasted a few hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 09.10.2022
- 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: unbekannt
Erholt: nein
Injection site erythema
Injection site inflammation
Injection site pruritus
Injection site warmth
Paraesthesia
Pruritus
Rash
Symptomtext
Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: Pt came in stating the area under her injection site on the left arm (about 2 to 3 inches below the injection site) was red and itchy starting last night. She showed me the area and it was about three inches in diameter and well below the injection site. It was red and inflamed looking and felt warm to the touch. I advised the pt to check with her dr office or an urgent care. Will follow up with the patient to check on how she is doing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 06.09.2022
- Beginn
- 28.03.2023
- Tage bis Beginn
- 203,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dysgeusia
Fatigue
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
3/28/2023 03:00 fatigue, chest congestion, runny nose. Tested with at home COVID-19 test, positive. Televisit with doctor who prescribed PAXLOVID and to treat symptomatically. That afternoon the PAXLOVID caused blood pressure to drop, and there was a very bitter taste in the mouth. After the 5-day course of PAXLOVID, I felt much better. There is a little chest congestion lingering at time of reporting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 28Mar2023 at home COVID-19 test, positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Type 2 Diabetes
- Andere Medikamente
- Verapamil; RABELAIS; metformin; SYNTHROID; VESICARE; lisinopril; liothyronine; atorvastatin; low dose aspirin; probiotic; cranberry pill; iron supplement; multivitamin
- Allergien
- Mineral oil; BACTRIM; NEOSPORIN; ZOSTAVAX (shingles vaccine); TRULICITY
- Vorherige Impfungen
- Shingles vaccine, ZOSTAVAX. Injection site reaction, a large and red reaction at the site. 55 2012; All 5 COVID-19 vaccines left
- Staat
- IL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 26.03.2023
- Impfdatum
- 13.09.2022
- Beginn
- 16.01.2023
- Tage bis Beginn
- 125,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Influenza like illness
SARS-CoV-2 test
Vaccine breakthrough infection
Symptomtext
NOTHING AT THE TIME. BREAKTHROUGH COVID IN JAN 2023. FLU LIKE SYMPTOMS FOR A DAY OR TWO. TIREDNESS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID TEST
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- RALOXIPHENE, VITAMIND3, calcium +D, zinc
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 11.01.2023
- Impfdatum
- 05.11.2022
- Beginn
- 05.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site bruising
Product storage error
Symptomtext
Site: Bruising at Injection Site-Mild, Additional Details: vaccine refrigerator temperature outside the recommended range
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 16.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint range of motion decreased
Pain
Symptomtext
This patient received a flu vaccine 9/16/22. Since administration, she states she has had decreased range of motion to left arm. She complains of pain with motion of left arm. She reports that symptoms are unchanging over the last 10 weeks. PRN ice has not helped. Pt was advised to follow up with her PCP asap for further evaluation and treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 29.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
Injection site bruising
Symptomtext
Vaccination appears to have accidentally been done intradermally based on post vaccine bruising and location of injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 09.10.2022
- Impfdatum
- 28.09.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site inflammation
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, Additional Details: patient called on 10/5/22 and said she received her flu vaccine on 9/28/22 and on 10/03/22, her arm below the injection site was red, inflamed, and itchy. She is out of town but I told her to keep an eye on it and see a doctor if it did not improve. not sure if its vaccine related, but patient was concerned so i recommended she see a doctor to get it checked out
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 04.10.2022
- Impfdatum
- 02.09.2022
- Beginn
- 29.09.2022
- Tage bis Beginn
- 27,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Symptomtext
Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 15.09.2022
- Impfdatum
- 09.09.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injection site erythema
Injection site swelling
Symptomtext
Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Additional Details: Patient went to urgent care to see dr.. she states she has had a reaction to a flu shot a couple years ago and thinks it must be an egg sensitivity
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 15.09.2022
- Impfdatum
- 26.08.2022
- Beginn
- 26.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Symptomtext
Site: Pain at Injection Site-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 13.09.2022
- Impfdatum
- 05.09.2022
- Beginn
- 05.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site induration
Injection site pain
Injection site rash
Injection site reaction
Injection site swelling
Injection site warmth
Insomnia
Nausea
Rash
Rash papular
Urticaria
Symptomtext
Site: Pain at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: Nausea-Mild, Systemic: Unable to Sleep-Medium, Additional Details: Hot and hard raised area at localized injection site. Got large round red welt on same inner arm (not injection site) with a darker center that is also raisted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site induration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 23.09.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 24,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
Rather sudden onset of sneezing, runny nose, and coughing. Temperature was 99.9 degrees. Pulse was 111. Oxygen level fluctuated between 84% and 94%. I took Tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 17OCT2022 - COVID-19 at home test - positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Calcium; Vitamin D3
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 04.10.2022
- Impfdatum
- 09.09.2022
- Beginn
- 20.09.2022
- Tage bis Beginn
- 11,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bradycardia
Cardiac pacemaker insertion
Catheterisation cardiac
Echocardiogram
Electrocardiogram
Symptomtext
Bradycardia, but no symptoms. Onset on 9/20/22. Problem resolved after pacemaker placed 9/23/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bradycardia
- Hospital-Tage
- -
- Labordaten
- Multiple ECGs on 9/21/22; left heart cath 9/22/22; Echocardiogram 9/23/22; pacemaker placement 9/23/22
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension, obesity, GERD
- Andere Medikamente
- I also received a high dose influenza vaccine at the ame time as the Covid booster. I developed complete heart block with a heart rate of < 50. I had no symptoms, and I was alerted by my Watch. I was seen at a local urgent care clinic, th
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 27.09.2022
- Impfdatum
- 26.09.2022
- Beginn
- 27.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Face oedema
Symptomtext
facial edema (left side of lip/ cheek) recommended Benadryl and to report to md asap for further consult. pt pt since sx onset at 4am her saw some improvement
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Face oedema
- Hospital-Tage
- -
- Labordaten
- TBD
- Aktuelle Erkrankungen
- none disclosed
- Vorgeschichte
- none disclosed
- Andere Medikamente
- none disclosed
- Allergien
- none disclosed
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 06.09.2022
- Beginn
- 06.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
flu clinic given at senior assisted living and care facility advisor instructed all patients over 65 and patient verbal confirmation when applicable but patient was actually 61 years old and was given HD FLUZONE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -