- Staat
- MI
- Alter
- 97,0
- Geschlecht
- F
- Eingang
- 13.04.2023
- Impfdatum
- 27.09.2022
- Beginn
- 09.04.2023
- Tage bis Beginn
- 194,0
- Dosis
- N/A
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute kidney injury
Acute respiratory failure
Angiogram pulmonary abnormal
Asthenia
Brain natriuretic peptide increased
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Dyspnoea
Escherichia urinary tract infection
Hypotension
Hypoxia
Illness
Intensive care
Lethargy
Lung infiltration
Oxygen saturation decreased
Pneumonia
Symptomtext
Discharge Provider: Primary Care Physician at Discharge: DO Admission Date: 4/9/2023 PRESENTING PROBLEM: Shortness of breath [R06.02] Hypoxia [R09.02] AKI (acute kidney injury) [N17.9] Elevated brain natriuretic peptide (BNP) level [R79.89] Multifocal pneumonia [J18.9] Sepsis with acute hypoxic respiratory failure and septic shock, due to unspecified organism [A41.9, R65.21, J96.01] COVID-19 [U07.1] Acute respiratory failure [J96.00] Acute respiratory failure with hypoxemia [J96.01] HOSPITAL COURSE: Patient is a 97 year old with extensive past medical history most significant for CAD, CKD, peripheral vascular disease, MR, hypertension with recent admission from 4/4-4/7 for weakness and near-syncope, diagnosed and treated for Ecoli UTI and diagnosed with COVID-19 on 4/4; presented to hospital ED 4/9 afternoon with dyspnea and lethargy. CXR and CTA with marked bilateral infiltrates suspicious for progression of COVID-19 pneumonia with possible bacterial pneumonia. Hypoxemic requiring HFNC 100%/55LPM. AKI on arrival. Discussion with patient's family established DNR/DNI status. Also developed hypotension and started on peripheral Norepi. She was admitted to MICU for ongoing management. Extensive conversations between providers and family detailed the severity of her illness and comorbidities likely to prevent recovery though continuing aggressive care to establish trajectory. By 4/10AM, off Norepi but still requiring HFNC 95%/55LPM with NRBM to maintain SpO2. AKI worsening. Noted worsening of oxygen needs with frequent desaturations 4/11. Family and DPOA at bedside - decision made to transition to comfort measures. Medical Examiner Case Assessment Select Applicable Patient Criteria: Does not meet any of the listed criteria
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Essential hypertension Carotid artery disease Osteoporosis Coronary artery disease involving native coronary artery of native heart without angina pectoris Mitral valve mass Hyperparathyroidism Low back pain Seasonal allergies Secondary hyperparathyroidism of renal origin Mitral valve insufficiency, unspecified etiology Stage 3b chronic kidney disease Leg weakness, bilateral Stress incontinence, female Goals of care, counseling/discussion Anemia in stage 3 chronic kidney disease Actinic keratoses Overactive bladder Other fatigue Vitamin D deficiency Other chronic sinusitis Dizziness Chronic nasal congestion Hoarse voice quality Chronic pain of right knee Recurrent UTI Blepharitis of upper and lower eyelids of both eyes Non-allergic rhinitis Ectropion due to laxity of eyelid, right Primary osteoarthritis involving multiple joints Primary insomnia Cerumen debris on tympanic membrane, left Fall Transient alteration of awareness Acute cystitis without hematuria Acute kidney injury Acute respiratory failure with hypoxemia Septic shock COVID-19
- Andere Medikamente
- acetaminophen (TYLENOL) 325 MG tablet amLODIPine (NORVASC) 5 MG tablet benzonatate (TESSALON) 100 MG capsule cholecalciferol (VITAMIN D3) 25 MCG (1000 UT) tablet guaiFENesin-dextromethorphan (ROBITUSSIN DM) 100-10 MG/5ML syrup metoprolol su
- Allergien
- CiprofloxacinDizziness, Edema CodeineNausea and Vomiting MorphineNausea and Vomiting NarcoticsNausea and Vomiting PravastatinMyalgia Sulfa DrugsNausea Only Vicodin [Hydrocodone-acetaminophen]Nausea and Vomiting
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 03.03.2023
- Impfdatum
- 30.09.2022
- Beginn
- 25.02.2023
- Tage bis Beginn
- 148,0
- Dosis
- N/A
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute myocardial infarction
Akinesia
Angiogram abnormal
Anticoagulant therapy
COVID-19 pneumonia
Cough
Dyspnoea
Echocardiogram
Echocardiogram abnormal
Ejection fraction decreased
Fatigue
Malaise
Sepsis
Stress cardiomyopathy
Troponin increased
Wall motion score index abnormal
Symptomtext
Discharge Provider: MD Primary Care Provider: Admission Date: 2/25/2023 Discharge Date: Mar 2, 2023 PRESENTING PROBLEM: NSTEMI (non-ST elevated myocardial infarction) (HCC) [I21.4] HOSPITAL COURSE: 89 y.o. female with h/o COPD on 2L at baseline, OSA, and HFpEF who presented 2/25/2023 to ED for malaise, fatigue, shortness of breath, and cough, no chest pain. Found to have elevated troponin and sepsis likely 2/2 to COVID Pneumonia. Cardiology consulted, TTE obtained with WMA concerning for atypical stress CMP with akinesis of the mid to distal anteroseptal and inferoseptal segments with preserved Apex wall motion. EF 26% previously 60-65%. Patient completed 48hrs of heparin drip. Upon discussion with cardiology she elected for a more conservative approach and was started on GDMT including metoprolol, spironolactone and Entresto. Plan was to proceed with a CMR and initiate dual anti-platelet therapy for year if there was any evidence of subendocardial infarct on the CMR. However repeat echocardiogram on the day of the planned CMR revealed left ventricular ejection fraction preserved at 59% with minor regional variation in the wall motion. Cardiology then deferred CMR as recovery of patient's cardiac function further confirms diagnosis of mid cavity variant stress-induced cardiomyopathy. Recommendations were made discontinue spironolactone and Entresto and continue your patient's beta blocker metoprolol. From a cardiology standpoint patient was safe for discharge and is to follow-up in the outpatient setting with Cardiology. Furthermore the pertains to patient's COVID pneumonia she completed a course of remdesivir, azithromycin, is to finish complete course of Decadron in the outpatient setting for 4 more days. Patient also received IV iron in the setting of iron deficiency anemia and ongoing cardiomyopathy. An incidental finding of thyroid nodule was noted on patient's CTA and she is to follow-up in the outpatient setting with primary care provider. Patient discharged in stable condition
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Community acquired pneumonia Chronic diastolic congestive heart failure (HCC) Chronic obstructive pulmonary disease with acute exacerbation (HCC) Type 2 diabetes mellitus without complication, with long-term current use of insulin (HCC) Essential hypertension, benign OSA (obstructive sleep apnea) Cecum thickening Asthma Thyroid nodule Mixed stress and urge urinary incontinence Malignant neoplasm of cervix (HCC) Incontinence of feces Hyperlipidemia Essential tremor Diastolic dysfunction Cognitive impairment Chronic respiratory failure with hypoxia and hypercapnia (HCC) Chronic pain of both shoulders Chronic pain of both knees Pneumonia due to COVID-19 virus Takotsubo cardiomyopathy
- Andere Medikamente
- acetaminophen (TYLENOL) albuterol (PROVENTIL) (2.5 MG/3ML) albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 ascorbic Acid (VITAMIN C) aspirin biotin cholecalciferol (VITAMIN D3) Coenzyme Q10 Cranberry cyanocobalamin dexam
- Allergien
- Zoster Vaccine LiveFatigue, Shortness of Breath LisinoprilCough
- Vorherige Impfungen
- Zoster Live Vaccine-Had severe reaction to Shingrix including SOB and Fatigue (03/11/2021)
- Staat
- NH
- Alter
- 6,2
- Geschlecht
- M
- Eingang
- 26.12.2023
- Impfdatum
- 03.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray normal
Computerised tomogram normal
Deep vein thrombosis
Pain in extremity
Peripheral swelling
Ultrasound Doppler abnormal
Symptomtext
Swelling + soreness left lower leg 48 hours post injections. Continued until MD visit 6 weeks post, (11/2023) when diagnosis of DVT left leg (ultrasound). All other tests (chest xray 11/2022), cat scan (02/22/2023), and diagnostic endoscope (June 21, 2023) ? all negative. Rx abixaban started (10mg x 2, then 5 mg x 2, currently 2.5 mg x2) and continuing. Possible link of DVT to simultaneous vaccinations of 10/03/2022 suspected upon preprint publication Oct 2023, and ACIP notice of October 2023 on possible link of simultraneous COVID and influenza vaccines among patients over 65-70 and ischemic stroke. Followup with Dr. (see above) 11/29/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- All imaging test negative (see above )
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- arthritis ? left knee (disgnosed but not treated)
- Andere Medikamente
- Timolol (drops) ; tamsulosi (0.4mg); latanoprost (drops)
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 08.11.2023
- Impfdatum
- 11.10.2022
- Beginn
- 09.06.2023
- Tage bis Beginn
- 241,0
- Dosis
- N/A
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Alanine aminotransferase increased
Angiogram pulmonary abnormal
Aspartate aminotransferase increased
Asthenia
Back pain
Blood creatinine increased
Blood potassium decreased
COVID-19
Chronic obstructive pulmonary disease
Computerised tomogram spine abnormal
Condition aggravated
Cough
Dyspnoea
Fall
Hiatus hernia
Hypokalaemia
Leukocytosis
Symptomtext
BRIEF OVERVIEW: Admission Date: 6/9/2023 Discharge Date: Jun 12, 2023 Discharge Disposition: home health care DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Hypokalemia [E87.6] Generalized weakness [R53.1] AKI (acute kidney injury) [N17.9] Fall, initial encounter [W19.XXXA] Left upper lobe consolidation [J18.1] COVID [U07.1] Compression fracture of thoracic vertebra, unspecified thoracic vertebral level, initial encounter [S22.000A] COVID-19 [U07.1] HOSPITAL COURSE: 72 y.o. female COPD requiring 2.5 L O2 at baseline presents to emergency department with complaint of cough and shortness of breath x 3 weeks. Seen by PCP prescribed a 9 day taper of prednisone, completed 7 days. Patient's husband had COVID about a month ago, but patient never tested positive. She unfortunately had her sandal caught and she sustained a fall . She presented with SOB and back pain . Patient presents to emergency department tachycardic with heart rate to 110. She was initially placed on 4 L via nasal cannula but was weaned down to baseline 2.5 L. labs remarkable for potassium 2.8, creatinine 1.55, AST 44, ALT 43. Patient has a leukocytosis of 14.7. COVID-19 positive. Procalcitonin was at 12.9. CTA thorax shows left upper lobe consilidation, mod-severe COPD, hiatal hernia and distal esophageal wall thickening, sclerosis and compression of T9. No evidence of PE. Patient was given 40 mEq of potassium and a 1 L normal saline bolus. CT lumbar and thoracic spine showed age-indeterminate moderate burst fracture T9. Seen and examined, husband and wife appreciative explained diagnosis, plans and need for ff up . Discharged hemodynamically stable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hx of adenomatous colonic polyps Moderate COPD (chronic obstructive pulmonary disease) HTN (hypertension) Gastroesophageal reflux disease without esophagitis Chronic respiratory failure with hypoxia Left upper lobe consolidation Nodule of upper lobe of right lung
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler ALPRAZolam (XANAX) 0.5 MG tablet Biotin 10000 MCG TABS buPROPion (WELLBUTRIN XL) 300 mg 24 hr tablet Coenzyme Q10 (
- Allergien
- Fosamax (Alendronic Acid)Itching, Asthma/Shortness of Breath Augmentin [Amoxicillin]Diarrhea, Nausea Only LatexRash Oxycodone-ibuprofenItching PenicillinsRash
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 03.03.2023
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Mobility decreased
Paraesthesia
Symptomtext
Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: numbess and tingling in legs difficult to move, went away in AM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Hypoaesthesia
Immunisation reaction
Injection site pain
Mobility decreased
Pain in extremity
Paraesthesia
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: numbness/tingling/pain from hips to feet, unable to move-Severe, Systemic: Numbness (specify: facial area, extremities)-Severe, Systemic: Tingling (specify: facial area, extemities)-Severe, Additional Details: numbness/tingling/pain from hips to feet, unable to move. Happened later in day when patient was home, was hospitalized and hospital came to decision that it was flu vaccine and asked to file VAERs report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 03.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Bone pain
Dizziness
Dyspnoea
Headache
Pyrexia
Swelling
Swelling face
Symptomtext
Patient stated swelling all over body and face, join and bone pain, headache, dizziness, difficulty breathing, and fever of 103
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- amiodarone eliquis
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 31.10.2022
- Impfdatum
- 28.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Musculoskeletal stiffness
Neuralgia
Odynophagia
Pain
Pain in extremity
Symptomtext
Patient reported having a sore arm later in the day after receiving vaccine. Then was having stiff neck and nerve pain whenever he moved his head and swallowing larger amounts of food. Was advised to take acetaminophen and ice packs to help with symptoms until Monday where his primary care physician could be contacted in order to further treat the symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hyperlipidemia, hypertension.
- Andere Medikamente
- Eliquis 5mg, Lisinopril 40mg, Pravastatin 80mg
- Allergien
- No allergies mentioned by patient.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
left arm pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, DM, R. Iliotibial Band Syndrome
- Andere Medikamente
- Albuterol inhaler, Lipitor, Betamethasone valerate topical cream, Calcium carbonate-vitamin D3, Lotrisone cream, losartan, metformin, omeprazole, triamcinolone ointment.
- Allergien
- Codeine, Naproxen Sodium
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling cold
Injection site erythema
Injection site pain
Injection site swelling
Injection site warmth
Pain
Somnolence
Symptomtext
Freezing cold Extreme body ache Slept 36 hours straight Soreness at injection site Large red, hot, swelling around injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hashimoto thyroid Obesity Fatty liver SVT
- Andere Medikamente
- Famotidine 20 mg HCTZ 25 mg Levothyroxine 0.075 mg Pravastatin 40 mg Vitamin C 250 mg Fish oil 1200 mg Aspirin 81 mg D3 50 mcg Centrum multivitamin
- Allergien
- None known
- Vorherige Impfungen
- Same symptom ps with COVID booster #1
- Staat
- OH
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 27.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Erythema
Flushing
Injection site erythema
Injection site rash
Pyrexia
Symptomtext
Pt called health department on 9/29/22 and reported his s/s started 9/28/22 with red rash on left arm near injection site and his face was flushed and appeared red. Pt reports he also felt like he had low grade fever for few days. Pt also reports he had chills. Pt reports he monitored his rash and fever at home. Pt reports he didn't take any OTC medications. Pt advised to call PCP for worsening s/s and states understanding. Pt said he didn't go to ER or to his family doctor since his injection. Pt reports as of 10/06/22 he is feeling better, face appearance normal, and rash is improved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- sarcoidosis, osteoarthritis, hypothyroidism, pacemaker/defibrillator
- Andere Medikamente
- levothyroxine, sotalol, athrotec
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- 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: ja
Inappropriate schedule of product administration
Symptomtext
This resident had already received a Pfizer Bivalent on 9/22/2022 but did not remember
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- MDD, HTN, Liver disease, spinal stenosis
- Vorgeschichte
- -
- Andere Medikamente
- none reported
- Allergien
- Morphine, Effexor, excederin, oxycontin, paxil
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 25.12.2022
- Impfdatum
- 17.12.2022
- Beginn
- 01.12.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Eye irritation
Oral discomfort
Symptomtext
Burning sensation In both knees, Eyes, Lips
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Burning sensation
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Sleep Apena High Pressure Blood nerve damage in both legs
- Andere Medikamente
- OXBUTYNIN 10mg 1XD AMLODIPINE 10mg 1XD GABPENTIN 300mg 3XD DULOXETINE 60mg 1XD ALPRAZOLAM 1mg 3XD
- Allergien
- PENCILLAN SEA FOOD
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 26.11.2022
- Impfdatum
- 03.11.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient was given a High Dose vaccine when they were under 65 years of age. Patient saw no adverse reactions from the vaccine. It was given by the vaccinating pharmacist at the clinic and reported when the pharmacy manager received all the documentation was received at the store.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 13.11.2022
- Impfdatum
- 29.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Skin warm
Swelling
Tenderness
Symptomtext
developed a red, slightly swollen, slightly warm, slightly tender 5 cm in diameter area on left arm noted the morning after the injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- right leg pain
- Vorgeschichte
- hypercholesterolemia
- Andere Medikamente
- simvastatin
- Allergien
- penicillin, sulfa
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
No adverse event
Symptomtext
Patient received a fluzone high dose quadrivalent vaccine on 10/1/2022 and then received another fluzone high dose quadrivalent 10/11/2022. There are no adverse effects being reported at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 04.10.2022
- Impfdatum
- 03.10.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Patient received a second flu shot in the season. Patient did not report receiving a flu shot already nor did he report receiving any vaccines in the past 4 weeks even though he received a High Dose flu vaccine 1 week prior.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 30.09.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
The incorrect vaccine was administered, patient was to receive FLUCELVAX 2022-23 PFS 0.5 ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -