- Staat
- -
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 05.10.2023
- Impfdatum
- 02.08.2022
- Beginn
- 25.08.2023
- Tage bis Beginn
- 388,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Angiocardiogram
Anticoagulant therapy
Asthenia
Atrial fibrillation
Atrial flutter
Blood culture negative
Blood thyroid stimulating hormone normal
CHA2DS2-VASc-score
COVID-19
Cardiac failure acute
Cardiac failure chronic
Chest X-ray
Condition aggravated
Cough
Diarrhoea
Diastolic dysfunction
Dyslipidaemia
Symptomtext
Patient is a 81 y.o. female patient of No, Physician with history of HTN, HLD, macular degeneration who presented to Hospital with flu like symptom . New onset atrial fibrillation with RVR Possible non-STEMI Prolonged Qtc Acute on chronic systolic and diastolic heart failure exacerbation Sp a total of 30 mg IV Cardizem bolus and Lovenox 1mg/kg at Ashland FSED. ChadVasc score: 4 (sex, age, HTN) Consult Cardiology, pending evaluation Check EKG - showing QTC >500, give 2 gram Mag Sulfate then repeat EKG. Echocardiogram report reviewed ejection fraction 20% and findings of mild diastolic dysfunction TSH. Within normal limits Serial Troponin, elevated but steady Lipid panel within normal limit A1c 5.8 Continue aspirin, statin. Continue heparin drip, cardiology on board consider CCTA left atrial appendage study and DCCV Start Cardizem drip on 8/25 then switch to esmolol drip per cardiology recommendation Continue IV Lasix S/p Esmolol DC Atrial flutter Discussed with cardiology at this point no plan for ischemic evaluation as an inpatient consideration outpatient stress test Status post heparin drip Continue aspirin, statin, beta-blocker, ARB and calcium channel blocker Acute Hypoxemic Respiratory Failure multifactorial secondary to fluid overload and COVID infection Currently requiring 3L per NC. Low flow oxygen protocol. Wean as tolerated. Scheduled/PRN bronchodilators sputum culture in progress urine antigens (strep/legionella), positive for Streptococcus pneumonia Continue IV rocephin day 5 Continue IV steroids and remdesivir, tomorrow will be day 5 then discontinue remdesivir DC oxygen via nasal cannula to assess oxygen on room air if remains stable above 95, consider discontinue IV dexamethasone We will discontinue IV dexamethasone Completing course of remdesivir today Covid-19 Virus Infection Streptococcus pneumonia antigen bacterial pneumonia Date of onset of symptoms: 8/21/2023 Symptoms present on admission: headache, nausea, cough, weakness, fatigue, sore throat, diarrhea Date of covid positive test: 08/24/2023 Vaccination status: vaccinated Imaging: CXR Oxygen requirements on admission: 3L Current oxygen requirements: 3L Medical therapy: steroids, PRN IV Lasix. Consultants following: cardiology and ID Anticipated special isolation end date: 8/30/2023. Follow blood and sputum cultures. Negative so far IV Rocephin since 8/25 IV remdesivir since 8/25, stop date 8/30 Consult ID, follow ID recommendations Essential Hypertension Continue Amlodipine and Metoprolol. Dyslipidemia Continue Atorvastatin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 02.08.2023
- Impfdatum
- 10.08.2022
- Beginn
- 03.02.2023
- Tage bis Beginn
- 177,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cerebrovascular accident
Transient ischaemic attack
Symptomtext
TRANSIENT CEREBRAL ISCHEMIA 2/3/2023 TRANSIENT CEREBRAL ISCHEMIA ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY 2/3/2023 TRANSIENT CEREBRAL ISCHEMIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 26.07.2023
- Impfdatum
- 25.08.2022
- Beginn
- 04.02.2023
- Tage bis Beginn
- 163,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
ACUTE RESPIRATORY FAILURE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 06.06.2023
- Impfdatum
- 04.02.2021
- Beginn
- 17.06.2022
- Tage bis Beginn
- 498,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
C-reactive protein increased
COVID-19
Fibrin D dimer
Nasal congestion
Procalcitonin
Prohormone brain natriuretic peptide increased
Pyrexia
SARS-CoV-2 test positive
Serum ferritin increased
Vaccine breakthrough infection
Symptomtext
BREAKTHROUGH COVID: FULLY VACCINATED and 2 BOOSTERS, COVID POSITIVE. . Diagnosis of Acute respiratory failure with hypoxia due to fever from corona virus disease 2019 infection. She has nasal congestion. She is requiring supplemental oxygen at 1 L. MEDICATED WITH DECADRON.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 6,0
- Labordaten
- CRP 74, D Dimer 1 ,Procal 0.16 ,Ferritin 371, pro BNP 2409
- Aktuelle Erkrankungen
- UNKNONWN
- Vorgeschichte
- dementia, AFib, HLD, HTN, osteopenia, GERD
- Andere Medikamente
- UNKNOWN
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 17.04.2023
- Impfdatum
- 23.08.2022
- Beginn
- 24.03.2023
- Tage bis Beginn
- 213,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Asthenia
Bacterial test
Blood creatine phosphokinase increased
COVID-19
Chest X-ray abnormal
Confusional state
Diarrhoea
Dyspnoea
Haematuria
Hypokalaemia
Legionella test
Lung infiltration
Myocardial ischaemia
Prohormone brain natriuretic peptide increased
Red blood cells urine positive
Rhabdomyolysis
SARS-CoV-2 test positive
Symptomtext
Patient is a 73 y.o. male patient of Physician No with history of COPD presented to a local Hospital with generalized weakness. Covid-19 Virus Infection, POA, currently improving Date of onset of symptoms: 3/23/2023 Symptoms present on admission: weakness, confusion, SOB Date of covid positive test: 3/23/2023 Vaccination status: vaccinated Imaging: CXR with left upper lobe infiltrate Oxygen requirements on admission: RA Current oxygen requirements: RA Medical therapy: not indicated Consultants following: ID Anticipated special isolation end date: 4/3/2023 Diarrhea, POA improving Likely due to COVID Patient reports it is improving. IV hydration and monitor. Possible community-acquired pneumonia X-ray of the chest showed possible left upper lobe infiltrates Ceftriaxone and azithromycin then discontinued as per ID recommendations. Strep and Legionella antigens Hypokalemia: Electrolyte replacement protocols Elevated Troponin: NSTEMI type II due to demand ischemia Elevated pro-BNP: Likely due to COVID Troponin 70; follow-up level 80. The patient does not have chest pain. No need for further testing. pBNP 3886 Follow-up with cardiology as an outpatient. Abnormal UA: Rhabdomyolysis UA positive for large amount of blood, but only 4 RBCs/hpf CPK 5787. Continue IV fluids. Follow-up urinalysis as an outpatient to confirm clearance of hematuria. COPD: Not in acute exacerbation Spiriva and Symbicort Albuterol PRN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 10.04.2023
- Impfdatum
- 28.07.2022
- Beginn
- 30.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac arrest
Catheterisation cardiac abnormal
Chest pain
Coronary arterial stent insertion
Dyspnoea exertional
Echocardiogram abnormal
Electrocardiogram abnormal
Fatigue
Myocardial infarction
Myocardial necrosis marker
Neck pain
Symptomtext
While walking to the mailbox patient became winded, fatigued, and felt crushing chest and neck pain. The patient called several family members. A family member arrived and insisted the patient go to the hospital. At the hospital, it was determined that Patient was in cardiac arrest and had suffered an MI. The attending ER (Dr. I believe was his name but can be easily verified through records) cardiologist (also cardiologist was on visiting/loan status from Cardio because local doctors were all out of town), stated, when I asked him if the COVID vaccine could have caused the heart attack, that yes it could have because the vaccine caused an inflammatory response.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- 4,0
- Labordaten
- ECG, cardiac enzyme tests, echocardiogram, catheterization, Dates 07/31/2022 Stent placed on 07/31/2022 lot 26409859
- Aktuelle Erkrankungen
- no illness
- Vorgeschichte
- na
- Andere Medikamente
- low dose blood pressure medication
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 21.02.2023
- Impfdatum
- 29.08.2022
- Beginn
- 13.09.2022
- Tage bis Beginn
- 15,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Cerebrovascular accident
Computerised tomogram head abnormal
Electrocardiogram
Gait disturbance
Hemiparesis
Laboratory test
Magnetic resonance imaging head abnormal
Symptomtext
Left side arm and leg weakness, difficulty walking. Patient reports symptoms started shortly after receiving vaccines. Went to the ER and was admitted, reports diagnosed with having had a stroke. Also reports having some cardiac testing while hospitalized, concerns of having a cardiac problem as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 5,0
- Labordaten
- CT scan and MRI EKG
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Previous cardiac surgery
- Andere Medikamente
- Diabetes medication, Plavix
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 01.02.2023
- Impfdatum
- 27.07.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 146,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Asthenia
COVID-19
Cardiac failure
Cardiac failure acute
Cardiac failure congestive
Chest X-ray abnormal
Confusional state
Culture urine positive
Dyspnoea
Enterococcal infection
Enterococcus test positive
Essential hypertension
Glycosylated haemoglobin increased
Hyperglycaemia
Hypoxia
Lung infiltration
Malaise
Symptomtext
The patient is a 65 y.o. female who presented to the the Hospital ED from home on 12/20/2022 with generalized weakness and dyspnea. ED work-up demonstrated acute on chronic respiratory failure believed secondary to CHF with contribution from covid 19 infection. Her hospitalization was prolonged due to persistent hypoxemia, confusion, and weakness requiring skilled facility placement after completion of COVID isolation. Assessment and Plan Acute on chronic hypoxemic respiratory failure Multifactorial related to decompensated heart failure and SARS-CoV-2 infection requiring supplemental oxygen above her reported baseline of 3-4 L/min -Responded to bronchodilator therapy and heart failure treatment -now on baseline 3L 02 Acute on chronic heart failure with preserved ejection fraction Essential hypertension Trigger initially reported as running out of medications, though this was denied by the patient -Outpatient regimen is noted to include metoprolol tartrate 12.5 mg twice a day, torsemide 50 mg daily, and spironolactone 50 mg daily -Responded well to IV furosemide she transitioned to torsemide 50 mg daily on 12/22/2022 with spironolactone resumed on 12/21/2022 Idiopathic bronchiolitis obliterans Known to clinic pulmonology medicine last assessed via telemedicine visit 12/12/2022; historically managed with nebulized budesonide and formoterol BID with a baseline oxygen level requirement of 3-4 L/min -Per telemedicine notes follow-up has occurred at 6-month intervals -Reinstated home budesonide/formoterol therapy via inhaler; plan for nebulizer at home -Continue albuterol PRN Obstructive sleep apnea Morbid obesity (BMI 39.72) Prescribed CPAP therapy to which she reports compliance; as above known to clinic pulmonary medicine, however, her home device is not available and there is concern it may have been lost in her moved. -Continue CPAP nightly and with napping if her home machine can be located SARS-CoV-2 infection / COVID-19 Presented with shortness of breath and generalized weakness - Symptom onset: 48 hours prior to arrival - Positive COVID-19: 12/21/22 - Vaccination status: vaccinated ( J&J 5/2021; boosted with Pfizer 7/27/2022) - CXR on admission showed infiltrates left greater than right and small left effusion - Oxygen status: up to 5 L/min with PRN bipap at presentation since weaned -completed course of decadron and remdesivir while in the hospital -Completed isolation while in the hospital Diabetes mellitus type 2 with hyperglycemia Baseline hemoglobin A1c at 7.7% in November 2022 with persistent elevations in the setting of dexamethasone use this admission -continue lantus/humalog and metformin on discharge Enterococcus faecalis urinary isolate Clinical relevance is not clear as the urinalysis and culture result from 12/27/2022 were performed based on order placed on 12/20/2022 -Given finding of Enterococcus species, favor treatment with amoxicillin; will complete 5-day course upon discharge Multiple sclerosis -Historical diagnosis reported to have been well controlled with baclofen, carbamazepine, and Avonex injections -She remains off Avonex injections in the hospital; she will be able to resume dosing at the facility with her home supply -Outpatient prescription records suggest this was prescribed 12/6/2022, though, it is not clear that this supply was received -She needs to establish with a local neurologist to reassess carbamazepine and baclofen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 13,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 14.12.2022
- Impfdatum
- 03.08.2022
- Beginn
- 06.12.2022
- Tage bis Beginn
- 125,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Diuretic therapy
Lower respiratory tract infection
Oxygen saturation abnormal
Renal impairment
Respiratory failure
SARS-CoV-2 test positive
Symptomtext
Discharge Provider: MD Primary Care Provider: DO Admission Date: 12/6/2022 Discharge Date: 12/8/2022 COVID positive Date: 12/6/2022 Clinical Narrative: Admitted for lower respiratory tract infection/pneumonia secondary to COVID. Renal dysfunction. Mild. Treated with Decadron and remdesivir. Was doing well 3 days and. Oxygen needs back to baseline. Did not wish to stay for a full 5 days of therapy. Please see below. He will be discharged this afternoon to the care of his family. Please see the following problem-list oriented Hospital Course below: * Pneumonia due to COVID-19 virus Assessment & Plan Prophylactic Zithromax in the setting of chronic obstructive pulmonary disease. Will give Decadron, vitamin- C, zinc, Pepcid and Remdesivir. Continue home Eliquis. 12/7 - was reportedly be on home oxygen but has not really complied with that. It is there for difficult to ascertain whether his oxygen needs early above baseline. There are some findings on his chest film consistent with a lower respiratory tract infection/pneumonia and he is being treated with remdesivir. We did discuss that this possibly could leave after 3 days of therapy should his symptoms not progress. He remains on corticosteroids as well. 12/8 - has remained stable. Discharge planning given continued stability Acute on chronic respiratory failure with hypoxia (HCC) Assessment & Plan Titrate oxygen to effect. Encourage prone positioning. Encourage pulmonary toilet. Bronchodilator p.r.n. Pulse oximetry. 12/8 - tolerated gentle diuresis. His oxygen needs are likely back to baseline as he had previously been prescribed home oxygen but was simply not wearing it
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Acute exacerbation of chronic obstructive pulmonary disease (COPD) (HCC) OSA on CPAP Pneumonia due to COVID-19 virus Acute on chronic respiratory failure with hypoxia (HCC) Essential hypertension Permanent atrial fibrillation (HCC) Vitamin D deficiency Colon polyps Gastroesophageal reflux disease without esophagitis Morbid obesity due to excess calories (HCC) Type 2 diabetes mellitus with diabetic polyneuropathy, with long-term current use of insulin (HCC) Seizure disorder, secondary (HCC) Stage 3a chronic kidney disease (HCC) Pure hypercholesterolemia Edema
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amLODIPine (NORVASC) 5 MG tablet benzonatate (TESSALON) 200 MG capsule budesonide/formoterol (SYMBICORT) 160-4.5 MC
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 23.08.2022
- Beginn
- 26.11.2022
- Tage bis Beginn
- 95,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Acute kidney injury
Acute respiratory failure
Anticoagulant therapy
Arterial catheterisation
Blood culture positive
Blood lactic acid increased
Bradycardia
Brain injury
COVID-19
Cardiac arrest
Cardiac monitoring abnormal
Cardio-respiratory arrest
Cellulitis
Central venous catheterisation
Chest X-ray abnormal
Citrobacter infection
Computerised tomogram abdomen abnormal
Symptomtext
COVID+ -unsure-early November per report. Vaccination status - Pfizer x4 Discharge Physician: MD Primary Care Physician: DO Date of Admission: 11/26/2022 Discharge Date: 11/27/2022 Room Number: BRIEF OVERVIEW: Active Hospital Problems Diagnosis Date Noted POA ? Acute hypoxemic respiratory failure 11/27/2022 No ? Hyponatremia 11/27/2022 Yes ? Lactic acidosis 11/27/2022 Yes ? Septic shock due to undetermined organism 11/26/2022 Yes ? Type 2 diabetes mellitus, without long-term current use of insulin 11/26/2022 Yes ? Cellulitis of right lower extremity 11/26/2022 Yes ? COVID-19 11/26/2022 Yes ? AKI (acute kidney injury) 11/26/2022 Yes ? Lung nodules 11/26/2022 Yes ? Hepatic steatosis 11/26/2022 Yes ? UTI (urinary tract infection) 11/26/2022 Yes ? Diarrhea 11/26/2022 Yes ? OSA (obstructive sleep apnea) 11/11/2020 Yes ? Multiple sclerosis, relapsing-remitting 08/24/2020 Yes ? Morbid obesity 02/17/2020 Yes ? HTN (hypertension) 08/31/2016 Yes ? Paroxysmal atrial fibrillation DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Severe sepsis [A41.9, R65.20] Cellulitis of right leg [L03.115] Acute cystitis with hematuria [N30.01] Combined abdominal pain, vomiting, and diarrhea [R10.9, R19.7, R11.10] Severe sepsis with septic shock (CODE) [R65.21] HOSPITAL COURSE: Patient is a 66-year-old female with a history of MS on Ocrevus, afib on xarelto, diabetes, OSA and obesity who presented for evaluation of fever, right leg pain and diarrhea. All of these symptoms had onset of <24 hours. In the ED the patient had severe lactic acidosis, leukocytosis along with fever, tachycardia and tachypnea. She was started on IV zosyn and IVF boluses. She had a CT abd/pelvis which was negative for acute process but did show right lung nodules and hepatic steatosis with recommendations for follow up nonemergent liver ultrasound and chest CT for further evaluation. Her UA was positive and urine culture was sent. The patient tested positive for COVID however she had COVID earlier this month and this was not felt to be a current infection. She had a negative CXR. She was admitted to the hospitalist team for further management of UTI, sepsis and cellulitis. Lactic acidosis and symptoms improved with IV fluids and Vancomycin + Ceftriaxone. Blood cultures positive for GPC, and lactic acid again began to increase. Antibiotics broadened to Vanc + Zosyn and patient transferred to ICU. She was awake and conversant and had acute onset of unresponsiveness with bradycardia on the monitor. Code was called and patient's rhythm was asystole. She received 40 minutes of CPR with multiple doses of epinephrine, vasopressin x1, and bicarbonate x1. ROSC was achieved. During the code, patient was intubated. General surgery was called in and performed arterial line and central line. Post arrest she was on levophed, vasopressin, stress dose steroids, Vancomycin, Cefepime, Metronidazole, and Clindamycin. Xarelto discontinued and pt transitioned to heparin gtt. Fluids transitioned to plasmalyte. Pt brought down for head CT which revealed no acute process with preservation of the gray-white matter differentiation. Patient transferred to ICU via ambulance with nursing care. Electrolytes were monitored and repleted throughout the admission. BRIEF OVERVIEW: Discharge Provider: MD Primary Care Physician at Discharge: DO Admission Date: 11/27/2022 DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Cardiac arrest [I46.9] HOSPITAL COURSE: 66 y/o female with hx of MS (Ocrevus), morbid obesity, OSA (CPAP), A fib (Xarelto), HTN, DM-2 and COVID (+) early November. She was admitted to Hosp 11/26 with RLE cellulitis, Citrobacter UTI, lactic acidosis, AKI, Strep pyogenes bacteremia and septic shock requiring vasopressors. Was also found to be again COVID-19 positive. Course was complicated by asystolic and PEA cardiac arrest early 11/27 which was preceded by labored breathing and hypoxemia. ROSC was achieved after ~ 40 minutes of CPR and patient was intubated after multiple attempts with vomiting during tube placement. CXR following intubation showed the development of diffuse bilateral airspace disease. Labs were significant for progressive AKI and worsened lactic acidosis. Head CT showed no acute abnormality. Transferred to ICU 11/27 with significant FIO2 and vasopressor requirements. CRRT started. Echo showed mild concentric LVH with no WMAs, normal systolic and diastolic function. cEEG without seizure but showed marked burst-suppression indicating severe encephalopathy. Course complicated by persistent lactic acidosis, transaminitis and thrombocytopenia. Repeat CTH suggestive of global anoxic brain injury. CT of RLE showed edema along superficial muscle fascia - evaluated by ortho - unlikely to be necrotizing fasciitis given clinical improvement (also very high surgical risk). CT of chest, abdomen, pelvis showed L>R airspace disease, fatty liver, mild anasarca, no bowel ischemia. MRI brain 11/30 with global hypoxic ischemic injury. Transitioned to comfort care. Time of death 1608 12/2/22. Family at bedside
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Pre-Existing Active Problems Diagnosis Date Noted POA ? Hyponatremia 11/27/2022 Unknown ? Lactic acidosis 11/27/2022 Unknown ? Septic shock due to undetermined organism 11/26/2022 Unknown ? Lung nodules 11/26/2022 Unknown ? UTI (urinary tract infection) 11/26/2022 Unknown ? Diarrhea 11/26/2022 Unknown ? Restless legs syndrome (RLS) 09/16/2022 Unknown ? Lumbar radiculopathy 09/16/2022 Unknown ? Sinus tachycardia 04/07/2021 Unknown ? Morbid obesity 02/17/2020 Unknown ? Dyslipidemia 08/31/2016 Unknown ? HTN (hypertension) 08/31/2016 Unknown ? Paroxysmal atrial fibrillation
- Andere Medikamente
- Acetaminophen 1,000 mg Oral Every 6 hours PRN Baclofen 10 MG TAKE 1 TABLET BY MOUTH THREE TIMES DAILY AS NEEDED FOR MUSCLE SPASMS D-Mannose 1,350 mg Oral Daily diazePAM 5 mg Oral Once PRN dilTIAZem HCl Coated Beads 240 MG TAKE 1 CAPSULE BY
- Allergien
- Bactrim [Sulfamethoxazole-trimethoprim]Rash AdhesiveSkin Rashes/Hives CodeinePalpitations Epinephrine Keflex [Cephalexin]Rash
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 07.11.2022
- Impfdatum
- 24.08.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 65,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
COVID-19 pneumonia
SARS-CoV-2 test positive
Symptomtext
Patient received Pfizer COVID vaccine on 4/1/21 (lot # ER8737), 4/26/21 (lot # ER8736), 8/29/21 (lot # FF2588), 3/4/22 (lot # FK9894), and 8/24/22 (lot # FP7137). On 10/28/22, patient admitted to our inpatient facility (med/surg unit) with acute hypoxic respiratory failure secondary to COVID-19 pneumonia and AKI superimposed on CKD s/p renal transplant. As of today (11/7/22), patient is still admitted in our med/surg unit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 10,0
- Labordaten
- COVID status positive 10/28/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- medical history significant for T1DM C/B CKD and deceased donor renal transplant for ESRD, HTN, HLD, MDD
- Andere Medikamente
- acetaminophen, acyclovir, aspirin, atorvastatin, belatacept inj, bupropion sr, vitamin d3, clopidogrel, diphenhydramine, estradiol patch, fiasp insulin pen, furosemide, tresiba insulin degludec pen, lisinopril, metoprolol er, mvi, mycopheno
- Allergien
- peanut, progesterone, amlodipine, cats, chorhexidine, oxycodone
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 24.08.2022
- Impfdatum
- 28.07.2022
- Beginn
- 11.08.2022
- Tage bis Beginn
- 14,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cerebrovascular accident
Symptomtext
Systemic: Stroke-Medium.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 30.08.2022
- Beginn
- 07.02.2023
- Tage bis Beginn
- 161,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
COVID-19
Cardiovascular deconditioning
Chronic kidney disease
Condition aggravated
Hypertensive emergency
Hyperthyroidism
Intensive care
Loss of personal independence in daily activities
Mobility decreased
Myocardial ischaemia
Pericardial effusion
Pneumonia
Therapy change
Troponin increased
Tympanic membrane perforation
Symptomtext
Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 2/7/2023 Discharge Date: 2/16/2023 HOSPITAL COURSE: History was obtained from the patient as well as extensive chart review which is highlighted and summarized below 87 y.o. male who has a past medical history of Anxiety, CAD (coronary artery disease), COPD (chronic obstructive pulmonary disease) (HCC), GERD (gastroesophageal reflux disease), Glaucoma, Gynecomastia, History of mammogram, HTN (hypertension), Hyperlipidemia, Hypothyroid, Macular degeneration, Osteoarthritis, PVD (peripheral vascular disease) (HCC), Renal insufficiency, Statin intolerance, Stroke (HCC), Testicular hypofunction, Thyroid cancer (HCC), and Type 2 diabetes with nephropathy (HCC). He initially presented to the hospital 1/27/23 for traumatic L tympanic membrane perforation and incidental diagnosis of COVID-19 infection. His hospital course was complicated by type 2 demand ischemic in setting of hypertensive emergency with troponin elevation as well as hospital acquired pneumonia and pericardial effusion. He required admission to ICU setting given requirement for multiple continuous IV antihypertensive drips. His home thyroid medication was decreased as there was thought that a component of iatrogenic hyperthyroidism could be contributing. He also developed AKI on CKD3, thought to be 2/2 ATN from hypertensive emergency. He was seen and evaluated by PT, OT, PM&R and felt to be an appropriate candidate for acute inpatient rehabilitation given cardiovascular deconditioning, impaired mobility and ADLs in setting of complex medical comorbidities as above and below. Transferred 2/7/2023
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mixed hyperlipidemia Essential hypertension Type II or unspecified type diabetes mellitus with peripheral circulatory disorders, uncontrolled(250.72) Peripheral vascular disease (HCC) Moderate COPD (chronic obstructive pulmonary disease) (HCC) History of thyroid cancer Other testicular hypofunction Gynecomastia Coronary artery disease involving native coronary artery of native heart without angina pectoris Type 2 diabetes mellitus with kidney complication, without long-term current use of insulin (HCC) CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (HCC) Medullary thyroid carcinoma (HCC) Hypercalcemia MEN, type 2 (HCC) Postoperative hypothyroidism Nocturnal hypoxia Facial droop Dysarthria Occlusion of right vertebral artery History of CVA (cerebrovascular accident) Chronic respiratory failure with hypoxia (HCC) Ischemic cardiomyopathy History of tobacco use Hypertensive renal disease with renal failure Perforated tympanic membrane Statin started by Vascular Surgery with Rx to be taken over by patient's PCP Debility
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amLODIPine (NORVASC) 10 MG tablet aspirin 81 MG chewable tablet calcium citrate-vitamin D (CITRACAL) 315-250 MG-UNI
- Allergien
- LescolJoint Pain PravastatinJoint Pain AliskirenMyalgia EvolocumabMyalgia FluvastatinMyalgia Hydralazine Lipitor [Atorvastatin]Joint Pain Niacin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 05.11.2022
- Impfdatum
- 26.08.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Computerised tomogram
Costochondritis
Echocardiogram
Electrocardiogram
Myocarditis
Pericarditis
Symptomtext
Developed mild myocarditis, milf pericarditis, and costochondritis, took steroids
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Echocardiograms (9/15)(9/20), multiple EKG (9/9)(9/15)(9/16)(10/19)(10/2) multiple rounds of bloodwork (9/9)(9/15)(9/16)(9/20)(10/2)(10/19) CT scan for pulmonary embolism (10/2)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Steroids
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 01.11.2022
- Impfdatum
- 21.08.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 66,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Thrombosis
Symptomtext
When I took my fourth Pfizer vaccine booster on 21Aug2022, I developed a new blood clot on 26Oct2022.; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 61-year-old male patient received BNT162b2 (BNT162B2), on 21Aug2022 as dose 4 (booster), single (Lot number: FP7137) at the age of 61 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. Concomitant medication(s) included: OLMESARTAN. Vaccination history included: coviD-19 vaccine (DOSE 3 (BOOSTER), SINGLE ((manufacturer unknown), I developed a blood clot on my right calf on 28Jan2022.), administration date: 26Nov2021, when the patient was 60-year-old, for Covid-19 Immunization, reaction(s): "blood clot on my right calf"; Covid-19 vaccine (Primary immunization completed (manufacturer unknown)), for Covid-19 Immunization. The following information was reported: THROMBOSIS (medically significant) with onset 26Oct2022 at 08:00, outcome "recovered" (2022), described as "When I took my fourth Pfizer vaccine booster on 21Aug2022, I developed a new blood clot on 26Oct2022.". Therapeutic measures were taken as a result of thrombosis. Clinical course: patient did not receive any other vaccines within 4 weeks prior to the COVID vaccine. When I took my 3rd vaccine on 26Nov2021 I developed a blood clot on my right calf on 28Jan2022. I was clear of the blood clot in Sep2022. When I took my fourth Pfizer vaccine booster on 21Aug2022 developed a new blood clot on 26Oct2022. Treatment received for blood clot was Blood thinner Xarelto 20 MG. Covid prior vaccination was yes. Covid was not tested post vaccination. Known allergies was none. Other medical history was none. The vaccine was administered on Pharmacy or Drug Store. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other medical history: None
- Andere Medikamente
- OLMESARTAN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 22.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 18.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Flushing
Hyperhidrosis
Hypotension
Injection site pain
Syncope
Tremor
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Vaso vagal syncope-Severe, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Severe, Systemic: Shakiness-Mild, Systemic: Weakness-Severe, Additional Details: Vaso vagal syncope
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 28.09.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back injury
Fall
Head injury
Syncope
Symptomtext
After administering the Pfizer Adult covid 19 vaccine Dose # 2 of the primary series, patient immediately stated he was claustrophobic,asked for me to open the side of the cubicle. I did and backed away from him. He immediately jumped up then stood by the cubicle entrance holding onto the cubicle side. Within seconds as I was counseling, he fainted . He fell directly backwards, hitting primarily his upper back and his head also but not as forceful. He was out for about 10-15 seconds, breathing ok, then slowly came to . laid for a few minutes, then sitting on the floor asking for water, then I got him the chair and pulled it out of the cubicle where he sat drinking the water until he felt ok to leave.Store management gathered information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- no testing
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- no known medications. only received pfizer covid 19, 2 primarys
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 17.09.2022
- Impfdatum
- 01.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest X-ray
Computerised tomogram
Dry throat
Dyspnoea
Electrocardiogram
Full blood count abnormal
Hypertension
Lung disorder
Pulmonary oedema
Tremor
Ultrasound scan
Vomiting
Symptomtext
This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 63-year-old female patient received BNT162b2 (BNT162B2), on 01Aug2022 at 11:00 as dose 4 (booster), single (Lot number: FP7137) at the age of 63 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Blood pressure problems" (ongoing), notes: Blood pressure problems. Concomitant medication(s) included: LOSARTAN taken for blood pressure measurement (ongoing); METOPROLOL taken for blood pressure measurement (ongoing). Vaccination history included: BNT162b2 (First dose, lot: EN6204, Route of administration: left arm), administration date: 22Mar2021, when the patient was 62-year-old, for COVID-19 immunization; BNT162b2 (Second dose, lot: ER8737, route of administration: left arm), administration date: 14Apr2021, when the patient was 62-year-old, for COVID-19 immunization; BNT162b2 (First booster dose, lot: FF8841, Route of administration: left arm), administration date: 16Nov2021, when the patient was 62-year-old, for COVID-19 immunization. The following information was reported: DRY THROAT (non-serious) with onset 2022, outcome "unknown", described as "Throat so dry"; VOMITING (non-serious) with onset 02Aug2022, outcome "unknown", described as "Puking"; TREMOR (hospitalization) with onset 02Aug2022, outcome "unknown", described as "Started having tremors"; DYSPNOEA (hospitalization) with onset 02Aug2022 at 09:30, outcome "unknown", described as "Having trouble breathing"; FULL BLOOD COUNT ABNORMAL (non-serious) with onset Aug2022, outcome "unknown", described as "Blood count was crazy"; HYPERTENSION (non-serious) with onset Aug2022, outcome "unknown", described as "Blood pressure was sky high"; PULMONARY OEDEMA (medically significant) with onset Aug2022, outcome "unknown", described as "Had fluid on lungs"; LUNG DISORDER (non-serious) with onset Aug2022, outcome "unknown", described as "Had two places on lung somewhere that was enlarged". The patient was hospitalized for dyspnoea, tremor (start date: 02Aug2022, discharge date: 03Aug2022, hospitalization duration: 1 day(s)). The events "had fluid on lungs", "blood count was crazy" and "blood pressure was sky high" required emergency room visit. The patient underwent the following laboratory tests and procedures: Blood test: (Aug2022) Blood Count was crazy; Chest X-ray: (Aug2022) Unknown; (Aug2022) Unknown, notes: a couple of chest X-rays; Computerised tomogram: (Aug2022) Unknown; (Aug2022) Unknown; Electrocardiogram: (Aug2022) Unknown; (Aug2022) Unknown, notes: two or three EKG's; Ultrasound scan: (Aug2022) heart is fine. Therapeutic measures were taken as a result of hypertension. Clinical course: Caller was a consumer who has received all Pfizer COVID Vaccine Doses and had a horrible reaction after receiving second booster dose Pfizer COVID Vaccine. Received second booster dose Pfizer COVID Vaccine on 01Aug2022 at 11:00. The next day, 02Aug2022 came to work and was fine. Having trouble breathing: At 09:30 on 02Aug2022 was sitting at work and kept thinking was having trouble breathing. Having trouble breathing got worse and worse. Started having tremors: Started having tremors. Started shaking really bad. Told boss had to go to hospital and went to #. Not caller's normal doctors, but was closest place to go. Really doesn't know for sure everything that happened. Knows could not quit shaking. Tried to do EKG and caller could not quit shaking, could not control shaking. Having trouble breathing: Could not breathe. Thought was going to die. Knows did EKG, chest X-ray and CAT scan, tons of blood work. Stayed overnight. Went into the emergency room at 10:00 and was there that night and next day until 17:30. Had fluid on lungs. Had two places on lung somewhere that was enlarged. Blood count was crazy. Blood pressure was sky high. Was puking. Stayed overnight: Clarifies was admitted to the hospital from the emergency room, sent upstairs and stayed a night on the floor. Having trouble breathing: Went away before came home from hospital. Doesn't think had any lasting effects. Hasn't had any trouble breathing since. Began once got to hospital on 02Aug2022. Hadn't eaten at 0930 and was puking just bile. Went away. The next day, 03Aug2022, was given food. Had no appetite but did try to eat a little bit. Ate some crackers and did not throw up anymore. Blood pressure was sky high was not still occurring. Does had blood pressure problems and taken blood pressure medicine, Metoprolol and Losartan. Metoprolol: Takes 50mg twice a day, takes once in morning and once at night. Losartan: 50mg, takes one and a half a day. Throat so dry wants to go get a drink and puts handler on hold. Caller stated received five doses Pfizer COVID Vaccine in total. Caller was confused about which doses received. Caller clarifies caller received four total doses of the Pfizer COVID Vaccine. History: Performed tests more than once. Clarifies, had one CAT scan, two or three EKG's and a couple of chest X-rays. Then scheduled for an echogram to make sure heart was working and pumping water off lungs. Had fluid on lungs. Heart doctor said heart was fine. Had to have another CAT scan to check the two things on lungs to make sure water is off lung. Does not know how is going to pay for this. If the patient was hospitalized from 02Aug2022to 03Aug2022. Blood pressure was sky high and takes blood pressure medicine Metoprolol and Losartan. Prior Vaccinations (within 4 weeks) there was no other vaccinations within four weeks prior to the first administration date of the suspect vaccine(s). No additional Vaccines Administered on Same Date of the Pfizer Suspect. No follow-up attempts are needed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary oedema
- Hospital-Tage
- 1,0
- Labordaten
- Test Date: 202208; Test Name: Blood work; Result Unstructured Data: Test Result:Blood Count was crazy; Test Date: 202208; Test Name: Chest X-ray; Result Unstructured Data: Test Result:Unknown; Test Date: 202208; Test Name: Chest X-ray; Result Unstructured Data: Test Result:Unknown; Comments: a couple of chest X-rays; Test Date: 202208; Test Name: CAT scan; Result Unstructured Data: Test Result:Unknown; Test Date: 202208; Test Name: CAT scan; Result Unstructured Data: Test Result:Unknown; Test Date: 202208; Test Name: EKG; Result Unstructured Data: Test Result:Unknown; Test Date: 202208; Test Name: EKG; Result Unstructured Data: Test Result:Unknown; Comments: two or three EKG's; Test Date: 202208; Test Name: Echogram; Result Unstructured Data: Test Result:heart is fine.
- Aktuelle Erkrankungen
- Blood pressure (Blood pressure problems)
- Vorgeschichte
- -
- Andere Medikamente
- LOSARTAN; METOPROLOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 02.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
patient passed out a few times . Ambulance was called and confirmed he only passed out . Patient reveled that he has a history of passing out with vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- per patient none
- Allergien
- per patient none
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 29.08.2022
- Beginn
- 29.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Hypoaesthesia
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting/Unresponsive-Medium. Additional details: Patient fainted after immunization given. Patient had some numbness in arms but was otherwise ok. Informed us at the store later in day that she was ok.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 29.08.2022
- Impfdatum
- 24.08.2022
- Beginn
- 24.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Confusional state
Loss of consciousness
Pallor
Retching
Urinary incontinence
Symptomtext
Pt came to Facility to receive menactra and first dose of covid 19 vaccine. Pt was given injection was t alking with nurse and parent when she became pale started gag like motion like she was going to vomit. Pt seated in chair then passes out loses incontinence of urine. Vitals are taken, at parent request 911 activated pt is out approx 5- mintues. Pt regains consciousness pt states she is confused. Pt vitals monitored pt is alert to name place DOB . EMS arrives pt walks to cot and is transferred to hospital per parent request. Vitals 14:15 Resp 12 unlabored BP 97/72 14:20 Resp 14 unlabored BP 102/78
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 25.08.2022
- Impfdatum
- 04.08.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Back pain
Blood test
Laboratory test
Pain
Thrombosis
Vaginal haemorrhage
Symptomtext
PATIENT PRESENTED BACK PAIN UPON WAKING ON FRIDAY 8/5/22 TO THE EXTENT OF NEEDING TO VISIT ER. VAGINAL BLEEDING WITH BLOOD CLOTTING BEGAN ON SATURDAY 8/6/22 AND CONTINUED SUNDAY 8/7/22. BLEEDING SUBSIDED MONDAY MORNING BUT BACK PAIN CONTINUED FOR FULL 10 DAYS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- ER BLOODWORK AND FOLLOW-UP PCP LABWORK WERE EXECUTED.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- PROGESTERONE MINI PILL, MULTIVITAMIN, PROBIOTICS
- Allergien
- PEANUT AND SHELLFISH
- Vorherige Impfungen
- VACCINES FOR TRAVEL IN MAY 2014 CAUSED RECTAL BLEEDING AT AGE 40 AND A SUBSEQUENT PE WITH HOSPITALIZATION AFTER RECEIVING A FLU
- Staat
- KY
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 22.08.2022
- Impfdatum
- 22.08.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Loss of consciousness
Nausea
Symptomtext
As patient was waiting the required 15 minutes after receiving her COVID booster, the patient reported passing out in her chair. Neither her nor her companion alerted staff until she came to. The patient stated she did not fall out of her chair but slumped in it, came to, had cold sweats and felt like she need to vomit but did not. Once staff was alerted, we went straight to her to see how she was doing. Patient said she was "fine." Companion stated she had not eaten anything since early this morning. Gave patient a sucker for sugar and asked her to wait an additional 15 minutes. After the additional 15 minutes patient stated she felt better and left the property.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 20.08.2022
- Impfdatum
- 16.08.2022
- Beginn
- 16.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Dizziness
Nausea
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Abdominal Pain-Medium, Systemic: Dizziness / Lightheadedness-Severe, Systemic: Fainting / Unresponsive-Mild, Systemic: Nausea-Medium.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 19.08.2022
- Impfdatum
- 04.08.2022
- Beginn
- 07.08.2022
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dizziness
Fatigue
Headache
Injection site pain
Lethargy
Pyrexia
Syncope
Unresponsive to stimuli
Symptomtext
Site: Pain at Injection Site-Mild, Systemic: Dizziness/Lightheadedness-Severe, Systemic: Exhaustion/Lethargy-Severe, Systemic: Fainting/Unresponsive-Medium, Systemic: Fever-Medium, Systemic: Headache-Severe, Systemic: Weakness-Severe.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 17.08.2022
- Impfdatum
- 17.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Disorientation
Dizziness
Respiration abnormal
Syncope
Symptomtext
Patient presented to pharmacy to receive their 2nd dose of Pfizer covid vaccine. Per patients father no adverse event reported with previous vaccination or any vaccination. Patient received the vaccine in the right arm and as we started to fill out the vaccine card the patient stood up to be closer to his father and fainted. The father prevented the patient from hitting his head on the ground and the patient had already woken up by the time of pharmacist getting to him. Patient was disoriented but began to respond to questions and asked what happened. The patient remained laying down for 5 minutes and attempted to sit in a chair. Was given orange juice and water as he had not eaten or drank since lunch around 2 pm He continued Upon sitting in the chair it was observed he began to breath heavier. Patient stated he felt dizzy and was again instructed to lie down and raise legs. Epipen was not administered but brought out in case of further reaction. Technician was called in to be ready to dial 911 if any other symptoms started. Patient was given 25 mg of Benadryl as it was the closet to vaccine room. He stated he was improving and did not have any more dizziness. Patient was kept lying down for 10 more minutes. Patient was then raised to a seated position against the wall and monitored for any more symptoms. After another 10 minutes patient felt well enough to stand. Father and pharmacist helped patient to his feet and held on to his arms in case of another reaction. Patient then sat in chair for another 5-10 minutes and was given a second dose of benadryl when discovered it was the 25 mg dose. Patient felt good and reported no symptoms after another 5-10 minutes and felt he could walk on his own. Patient was walked out while pharmacist carried an epi pen with the to ensure it was available if needed. Patient stated they felt no more symptoms and. Father was asked if he had any questions or concerns. Instructed father that if any other symptoms start again he is to be taken to emergency room. Father said he understood. In total around 45 minutes to 1 hour of attention were given to patient to ensure treatment was readily available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None besides observation.
- Aktuelle Erkrankungen
- NON PROVIDED
- Vorgeschichte
- NON PROVIDED
- Andere Medikamente
- NONE
- Allergien
- NONE PROVIDED
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 10.08.2022
- Impfdatum
- 29.07.2022
- Beginn
- 08.08.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bacteraemia
Condition aggravated
Epilepsy
Feeling cold
Headache
Hypotension
Nervousness
Pneumonia
Pyrexia
Seizure
Sepsis
Symptomtext
8/7/2022- Assitant to the family calling for acute constant severe fever (101.5 currently), headache and intermittent seizures "every night" since pt received immunizations (TDAP, Polio, Covid-19, Hep A and HPV) at Health Dept on 7/29. Per pt's father pt "feeling cold and shaky". Pt is awake and alert per pt's father. Pt has hx of seizures but from symptoms reported by pt's family the number of seizures pt has been having has increased since pt received the 5 immunizations. PT reached out to pt's neurologist on 8/5 r/t reported seizures and neurologist recommended increasing pt's Keppra medication to 750 mg BID per note in pt's chart. Per note in pt's chart neurologist staff were not able to reach pt's family to inform them of the increase in medication dosage. Pt's family denies receiving message regarding increasing pt's Keppra medication dose. Symptoms started 7/29. Pertinent negatives include: No chest pain. No breathing difficulty. No cyanosis. No diarrhea. No vomiting. No cough. No known exposure to Covid-19. No symptoms of dehydration, still urinating with normal frequency. Patient unknown. Patient presented to Hospital on 8/7/22 and is currently admitted (as of 8/10/22) for; Hospital Problem List Epilepsy, unspecified, not intractable, without status epilepticus Left lower lobe pneumonia Sepsis due to pneumonia Fever in pediatric patient Hyponatremia Leukocytosis Hypotension Bacteremia due to Gram-positive bacteria
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hospital Epilepsy, unspecified, not intractable, without status epilepticus Left lower lobe pneumonia Non-Hospital Immigrant with language difficulty Encounter for health examination health examination Decreased appetite Transaminitis Thrombocytopenia On valproic acid therapy Postural instability Allergic rhinitis, unspecified seasonality, unspecified trigger
- Andere Medikamente
- acetaminophen (TYLENOL) tablet 650 mg cefTRIAXone 40 mg/mL in dextrose (ROCEPHIN) IVPB 2,000 mg diazePAM (VALIUM) tablet 2.5 mg diazePAM (VALIUM) tablet 2.5 mg diazePAM (VALIUM) tablet 2.5 mg divalproex (DEPAKOTE ER) 24 hr tablet 1,000 mg i
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Nausea
Syncope
Symptomtext
FELT NAUSEATED, WOOZY., FAINTED BUT VERBAL FOR SOMETIME THEN RECURRED AGAIN, EMT RESPONDED TO THE ORIGNAL INCIDENT. OVERALL COMPLAINT:- FAINTING
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- brain aneurysm, seizures
- Andere Medikamente
- unknown
- Allergien
- unknown. not listed
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 09.11.2023
- Impfdatum
- 15.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyskinesia
Paraesthesia
Pruritus
Symptomtext
started having like involuntary muscle movements on different parts of body like legs, arms, face shoulders, stomach, etc.; started feeling itchiness all over body without getting any redness on skin; sometimes felt like a needle on some parts of body like hands or feet or back or neck, etc.; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 60-year-old male patient received bnt162b2 (BNT162B2), on 15Aug2022 at 11:30 as dose 1, single (Lot number: FP7137) at the age of 60 years, in left arm for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: PARAESTHESIA (non-serious) with onset 17Aug2022 at 22:45, outcome "not recovered", described as "sometimes felt like a needle on some parts of body like hands or feet or back or neck, etc."; PRURITUS (non-serious) with onset 17Aug2022 at 22:45, outcome "not recovered", described as "started feeling itchiness all over body without getting any redness on skin"; DYSKINESIA (non-serious) with onset 17Aug2022 at 22:45, outcome "not recovered", described as "started having like involuntary muscle movements on different parts of body like legs, arms, face shoulders, stomach, etc.". The events "started having like involuntary muscle movements on different parts of body like legs, arms, face shoulders, stomach, etc.", "started feeling itchiness all over body without getting any redness on skin" and "sometimes felt like a needle on some parts of body like hands or feet or back or neck, etc." required physician office visit and emergency room visit. Therapeutic measures were taken as a result of dyskinesia, pruritus, paraesthesia. Reportedly, the patient had some steroids and some kind of allergy medication. Additional information: The patient did not have Covid prior to vaccination and he was not tested positive post vaccination. Reportedly, no known allergies or other medical history. Also, no other vaccine in four weeks or other medications in two weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: known allergies: no other medical history: no
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 16.06.2023
- Impfdatum
- 21.04.2023
- Beginn
- 24.04.2023
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Condition aggravated
Cough
Dry eye
Dry mouth
Laboratory test abnormal
Nasal discomfort
Pain
Pyrexia
Respiratory tract congestion
Sjogren's syndrome
Sneezing
Urine analysis
Symptomtext
After I received the bivalent booster on 4/22/23, I experienced the normal side effects I had gotten from the four previous Covid vaccines (low-grade fever, body aches, and chills for 48 hours). Then on day 3 following the vaccine, I experienced burning in my nose, congestion, coughing, sneezing until day 8. Those symptoms resolved on their own. But since receiving the bivalent vaccine, I have expeienced a worsening of my Sjogren's symptoms - my dry eyes have gotten much worse, and my mouth dryness has gotten much worse. It has continued over the past two months (to the present). I made an appointment with the rheumatologist and opthamologist. The rheumatologist had me complete blood work and urinalysis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Blood work and urinalysis done on 5/11//23 and again on 5/15/23 for the rheumatologist when my Sjogren's symptoms worsened. Some of the lab results were abnormal and will repeat them
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Sjogren's Syndrome, Crohn's
- Andere Medikamente
- Crestor, Actonel, Tyrvaya, blood serum eye drops, vitamin D3
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 13.04.2023
- Impfdatum
- 22.08.2022
- Beginn
- 05.04.2023
- Tage bis Beginn
- 226,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
COVID-19
Chest X-ray abnormal
Computerised tomogram thorax abnormal
Condition aggravated
Fatigue
Leukocytosis
Lung opacity
Myalgia
Pneumonia
Procalcitonin increased
Pyrexia
Respiratory tract infection
SARS-CoV-2 test positive
Sepsis
Symptomtext
Discharge Provider: MD Primary Care Provider at Discharge: MD Admission Date: 4/5/2023 Discharge Date: 4/10/2023 PRESENTING PROBLEM: Respiratory infection Sepsis due to pneumonia Sepsis, due to unspecified organism, unspecified whether acute organ dysfunction present COVID Sepsis HOSPITAL COURSE: Patient is a 61 y.o. male with prior medical history of progressive MS, chronic pain, depression, GERD, OSA who presented to hospital on 4/5/2023 with progressive weakness and fatigue. The patient was found to be have Sepsis and COVID-19 positive upon arrival to the emergency department. Initial chest x-ray performed in the emergency department showed concern for right axillary mass however CT of the chest did not visualize in the right axillary mass or lymph node enlargement. Was noted to have mild left and right basilar streaky ground-glass opacities. He received an initial dose of azithromycin and ceftriaxone and was monitored off for 24 hours. Due to no leukocytosis or elevation of procalcitonin. The patient then developed elevated fevers and an elevated procalcitonin and leukocytosis on 04/07/2023 and the antibiotics were resumed due to post-viral community acquired pneumonia. While hospitalized he completed a 5 day course of azithromycin and ceftriaxone. He also received 5 days of remdesivir. He will be discharging home with continued home health care services. Discharge doing with the Mucinex as well as p.r.n. albuterol inhaler. Due to myalgias he was also given a 3 day script for Norco as this has been helping with the symptom control. Recommend post hospitalization follow-up with PCP in 1 week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic pain Enthesopathy of hip region Bursitis of hip, right GERD (gastroesophageal reflux disease) Trigeminal neuralgia Legal blindness History of pulmonary embolism Wheelchair dependence Chronic headache Dysphagia Blindness of both eyes Hypophonia Neuropathic pain Spastic quadriplegia secondary to multiple sclerosis Multiple sclerosis, secondary progressive Dysphagia following unspecified cerebrovascular disease OSA (obstructive sleep apnea) Senile osteoporosis Recurrent cellulitis of lower extremity Benign essential HTN Age-related osteoporosis without fracture Sepsis due to pneumonia COVID-19
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet albuterol (PROVENTIL) (2.5 MG/3ML) 0.083% nebulization Alpha-Lipoic Acid 600 MG CAPS Ascorbic Acid (VITAMIN C) 500 MG CAPS aspirin 81 MG enteric coated tablet baclofen (LIORESAL) 10 MG tablet Calcium Ca
- Allergien
- NystatinHives VancomycinRed man syndrome Adhesive Tape TapeRash
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 20.10.2022
- Beginn
- 27.02.2023
- Tage bis Beginn
- 130,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
Pt has a PMH of COPD with chronic hypoxic respiratory failure and is on 2.5 L nasal cannula. She presents to the ED with 3 days of worsening shortness of breath. Her O2 sats were in the mid 80s and she is not requiring 4L. She has a nonproductive cough and was found to be COVID positive. She was admitted due to COVID positivity and COVID exacerbation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 03.10.2022
- Beginn
- 22.01.2023
- Tage bis Beginn
- 111,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Haemorrhage
Joint swelling
Limb discomfort
Mobility decreased
Skin discolouration
Symptomtext
Hemorrhage right index finger, middle joint, swelling, discoloration, tightness, lack of mobility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 30.11.2022
- Impfdatum
- 28.11.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Peripheral swelling
Symptomtext
patient states arm and shoulder are swollen and having trouble lifting arm up
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- no medications listed in patient profile.
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 07.11.2022
- Impfdatum
- 03.08.2022
- Beginn
- 26.08.2022
- Tage bis Beginn
- 23,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram
Hypoaesthesia
Muscle spasms
Pain
Pain in extremity
Paraesthesia
Ultrasound Doppler
Symptomtext
I have muscle spasms in my upper and lower arm and the pain radiated into my hands. I had tingling in fingers numbness in my thumbs. It was just extreme pain anytime I moved my arms and even let it hand independently. The pain is still there just not as intense.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- EKG; Doppler on left arm; Nerve test in near future.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetes; Hight blood pressure
- Andere Medikamente
- Aspirin; ALLEGRA; TRULICITY; DITROPAN XL; JARDIANCE; WELLBUTRIN XL; AMARYL; ALDACTONE; LIPITOR; NORVASC
- Allergien
- Chocolate; fish; nuts
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 24.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Blood test normal
Chest X-ray normal
Fatigue
Hypertension
Influenza virus test negative
Productive cough
SARS-CoV-2 test negative
Sinus congestion
Symptomtext
Around two weeks before receiving my vaccine, I was experiencing an upper respiratory infection. However, I had finished my round of antibiotics and was feeling better. After receiving the vaccine, I did notice a bit more of a cough but by the following Wednesday, my cough was really bad again. The cough was not productive at that point. I was very congested in my sinuses and very fatigued. I was trying to treat my cough with over-the-counter medication, but I continued to not feel well. Friday, I traveled out of town to see family, but I was feeling so bad by Saturday afternoon that I had to go home. I went to the local emergency room since none of the urgent clinics were open. When I arrived at the hospital, my blood pressure was extremely high. I had no chest pain, but my cough was uncontrollable. They did blood work to check my heart, kidney, and liver function. All of that came back normal. They did chest x-rays and found nothing. I also tested negative for COVID-19 and Flu. The doctor prescribed a medication for my blood pressure and advised that I continue using my inhaler and discontinue using any over the counter medication for fear of raising blood pressure. They also prescribed a cough medicine, Prednisone, and Flonase. I wasn't able to begin those until late in the afternoon on Sunday. I followed up with my doctor on Wednesday, who increased the blood pressure medication and then advised that I increase my inhaler usage as well. He also prescribed Teflon Pearls for coughing. By Friday, I was still coughing some, but it was more productive. After increasing the medications, I have begun to improve a lot more quickly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- 10/15/2022- Blood Work- Normal; Chest X-ray- Nothing Found; COVID-19 Test- Negative; Flu Test- Negative
- Aktuelle Erkrankungen
- Upper Respiratory Infection
- Vorgeschichte
- Asthma
- Andere Medikamente
- Vitamin D; Adderall
- Allergien
- Penicillin; Azithromycin; Bromide
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 03.10.2022
- Impfdatum
- 21.07.2022
- Beginn
- 21.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysaesthesia
Paraesthesia
Symptomtext
Persistent paresthesia and sometimes dysesthesia in limbs (upper and lower) that is one sided, but shifts from side to side.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 28.09.2022
- Impfdatum
- 17.08.2022
- Beginn
- 18.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Angiopathy
Arthralgia
Chest pain
Computerised tomogram
Eye pain
Gingival pain
Pain
Pain in extremity
Pyrexia
Symptomtext
Same as what I reported after 1st dose of Pfizer vaccine. 103 degree fever, blood vessels felt like they were constricting which resulted in severe chest pain. Additionally, throbbing pain behind my right knee. Also, had pain in my eyes, gums, and toes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Cardiac cat scan on 9-21-22
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- crestor
- Allergien
- none
- Vorherige Impfungen
- Yes, my first shot of Pfizer. (this event being reported is my 3rd Pfizer shot.
- Staat
- FL
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 25.09.2022
- Impfdatum
- 20.09.2022
- Beginn
- 20.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Injection site pain
Mobility decreased
Pain in extremity
Pruritus
Rash
Symptomtext
Site: Pain at Injection Site-Medium, Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Additional Details: Patient's arm was sore. SHe has limited mobility but I dont think she was not really trying. She had a rash that appeared on her wrist later in the evening on the day of the shot. They were asking me if it was from a bite. I could not tell, could have been either or. I gave her allegra because she did not want benadryl. I told her she should get better everyday, if gets worse to let us know and her doctor. She did not have difficulty breathing or any other issue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 17.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Injection site pain
Injection site swelling
Lymphadenopathy
Pain
Pyrexia
Tremor
Symptomtext
Fever up 103?, chills, shaking, aches, injection site pain and swelling, swele).ling of lymph nodes under arms - more so on left (injection side)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, GERD, Sleep apnea, obesity
- Andere Medikamente
- Omeprazole, liotyronine, levothyroxine, allopurinol, Allegra, V C, B complex
- Allergien
- Sulfa antibiotics, oxycodone, hydrocodone, nalfon, gluten, mold, mildew
- Vorherige Impfungen
- Same to all three other Pfizer Covid shots but of longer duration. Mild two to three day injection site and fatigue with regul
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 09.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Blood pressure increased
Chest pain
Dyspnoea
Lethargy
Symptomtext
Individual became anxious and stating unable to breathe and feeling lethargic. She was experiencing chest pain and in pending doom. She suffers from anxiety and takes medication on and off. Her vitals signs were the following: 6:45pm B/P 170/110, HR - 95, O2 at 97 %, Resp. 16, at 6:51 B/P - 154/98, 7:01 B/P 144/92. EMS called due to the patient still c/o of feeling chest pain and lethargic. Paramedics arrived and B/P was higher. Patient was transported via to Doctor's Hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Suffers from Anxiety and Panic Attacks
- Vorgeschichte
- Obesity/Hypertension
- Andere Medikamente
- Takes medication for anxiety
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 16.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthma
Dyspnoea
Pruritus
Urticaria
Rash
Symptomtext
Severe hives on face, neck, arms, chest and back Severe Itching Asthma flare up Difficulty breathing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Pfizer Covid Vaccine
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Crohn's Disease
- Andere Medikamente
- Humira Albuteral Vitamin D Claritin Singular
- Allergien
- All Seafood All Nuts
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 16.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthma
Dyspnoea
Pruritus
Urticaria
Rash
Symptomtext
Severe hives on face, neck, arms, chest and back Severe Itching Asthma flare up Difficulty breathing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Pfizer Covid Vaccine
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Crohn's Disease
- Andere Medikamente
- Humira Albuteral Vitamin D Claritin Singular
- Allergien
- All Seafood All Nuts
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 06.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injected limb mobility decreased
Pain
Symptomtext
Pt stated she is having trouble lifting her arm up. She said its painful. No visible inflammation on the arm at all.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- none reported by patient
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 02.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chest pain
Lip swelling
Vomiting
Symptomtext
Severe vomiting, chest pain, little swelling of the lips Went to ER , treated with anti emetic, Benedryl, discharged to home , doing well
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 23.08.2022
- Impfdatum
- 19.08.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Dry mouth
Epistaxis
Nausea
Paraesthesia
Tremor
Symptomtext
Systemic: Chills-Medium, Systemic: Dizziness / Lightheadness-Mild, Systemic: dry mouth and nose. had a nose bleed 10 mins after vaccination, stopped with pressure-Severe, Systemic: Nausea-Medium, Systemic: Shakiness-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 16.08.2022
- Impfdatum
- 16.08.2022
- Beginn
- 16.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mobility decreased
Pain in extremity
Symptomtext
Patient confirms she was fine prior to the injection. Injection done in the left arm but having pain in the right-side, which prevents her from lifting her right arm properly.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Pulmonary embolism
- Andere Medikamente
- Lisinopril and Warfarin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 06.08.2022
- Impfdatum
- 31.07.2022
- Beginn
- 31.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Limb injury
Paraesthesia
Symptomtext
Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 03.08.2022
- Impfdatum
- 03.08.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Limb discomfort
Paraesthesia
Symptomtext
Per patient, around 10 am she received her Pfizer shot. During her 15 min observation period (after the shot while), she sat in the pharmacy area. She started to feel tingling in her calf, so she moved around and felt better. Around dinnertime, she felt as if something was biting her legs, so she removed her tights (she thought they were too tight). After removing the tights, her legs felt needle-like biting, which also spread to her arms. She said her skin is fine. No bumps, hives or redness. Recommended following-up with physician.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 03.08.2022
- Impfdatum
- 24.07.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arrhythmia
Dizziness
Dyspnoea
Dyspnoea exertional
Exercise tolerance decreased
Extrasystoles
Total lung capacity decreased
Symptomtext
Beginning about 48 hours after vaccine and continuing since (now on day 7): mild heart arrhythmia, heart feels like it's skipping a beat on occasion. Frequency has ranged from once every 10 seconds to once per minute or less. I thought it might be caffeine related so I quit coffee for about 4 days, but no impact. Some light dizziness or faint-headedness on occasion. Lung capacity feels reduced, I get winded doing activity that is not strenuous. Yawning or taking a deep breath feels more difficult than before. I rode my bike 28 miles in one morning just 6 weeks ago, but canceled a neighborhood ride with a friend on day 3 after the booster for fear I might pass out or trigger a heart event. This feels like something that I've heard others report as being symptoms of 'long covid,' and I did have covid last year, but I have not experienced these issues until now. My symptoms during covid were moderate to mild, and my only lingering symptom was a persistent cough for about a month, which has cleared.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- None yet. I do not have insurance.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None.
- Andere Medikamente
- None
- Allergien
- Aleve. No food allergies.
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Blood pressure increased
Chest discomfort
Dizziness
Hypertension
Tachycardia
Symptomtext
Pt c/o dizziness and chest tightness approximately 20 minutes post vaccination. Observation revealed no visible sign of hypersensitivity. No injection site reaction was noted. No swelling of tongue, lips, or throat. Pt was able to carry on regular conversation without dyspnea, wheezing, or coughing. Pt was not diaphoretic. Pt was hypertensive and tachycardic as noted below. Pt reported taking her daily BP meds already today. Pt denied chest/back pain, nausea, or left-arm pain. Impression was that this was anxiety-induced, but could not rule out cardiovascular origin. Instructed pt to continue monitor BP once home and contact PCP if remained elevated. Instructed pt to contact 911 if symptoms progressed or developed consistent with cardiac event. Attempt to contact pt by phone later in the day was not answered. Voicemail was left, but no reply by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- blood pressure was noted as elevated on 2 measurements: 167/93 and 163/101. HR was 82 and 90bpm.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- metformin, venlafaxine, benazepril, levothyroxine, np thyroid, spironolactone, montelukast
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 29.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Hypotension
Rash
Urticaria
Symptomtext
She received the vaccine around 11AM and about 2 hours later she started having a rash on the right side of her face and some hives. About 1:35PM it spread to the left side of her face. At 1:50PM I gave her Benadryl and she started improving after that. We went to see the Urgent Care Dr. about 2:45PM and they checked vitals were ok. Her blood pressure was a little low at first, but it they determined it was ok.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Cephalasporin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 23.10.2023
- Impfdatum
- 20.10.2023
- Beginn
- 20.10.2023
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Injection site pain
Nausea
Pyrexia
Tinnitus
Symptomtext
the same evening as vaccination had tinnitus thru the night. Beginning the next afternoon ran a low grade fever (100 ish) off and on thru the next day. Also have experience some nausea and slight headache in the days since the vaccination. Sore injection site for 2 days also. Took ibuprofen for the headaches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- crestor
- Allergien
- valium, demerol, scallops, melons
- Vorherige Impfungen
- The first COVID vaccine I experienced the tinnitus for a day as well as insomnia for 2 weeks.
- Staat
- MA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 05.08.2023
- Impfdatum
- 10.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 7,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Anti-cyclic citrullinated peptide antibody positive
Arthralgia
Autoimmune disorder
Blood test abnormal
C-reactive protein increased
Gait disturbance
Impaired quality of life
Impaired work ability
Inflammation
Inflammatory marker increased
Myalgia
Neuralgia
Orthosis user
Pain
Pain in extremity
Red blood cell sedimentation rate increased
Rheumatoid arthritis
Rheumatoid factor positive
Symptomtext
I had Moderna for my first vaccines. The fifth dose, booster was my first pfizer on 8/10/2022. A week later I could barely walk due to acute inflammation and pain. I struggled for months with overall joint, muscle, nerve pain throughout my body, particularly in my ankle, knees and legs. The inflammation and pain has seriously impacted my quality of life. I saw my primary physician for examination and bloodwork and she referred me to a rheumatologist due to the highly elevated inflammation markers in my blood and a positive RA factor which I have never had before. I could barely function at work as a teacher. My life consisted of managing pain with NSAIDS, joint braces, ice packs etc. It took over my life. Finally I got an appointment with the Rheumatology Clinic in November, 2022. I was then treated with 400 mg Plaquenil and naproxen as well as high doses of Vitamin D. Follow up 4 months later in March showed some improvement in symptoms. I then began Physical Therapy for 12 weeks. Almost a year after my pfizer booster, i am still suffering with pain and inflammation, and the recent visit to Rheumatology clinic recommended that i remain on Plaquenil indefinitely. I may have to deal with Auto immunity Disease, RA, for the rest of my life. I walk with a noticable limp, as my righ leg is still the most impacted. Prior to this Vaccine Injury on 8/10/2022, I was perfectly healthy. I did not take any medications regularly, had no chronic health conditions, and enjoyed an active healthy lifestyle. This Covid 19 , pfizer vaccine Injury has not only stolen this past year of my life, but the future outcome and impact is still uncertain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Abnormal: 10/28/22 - C Reactive Protein 33.5 mg/L, ESR - 31, RA factor - 53, CCP IgG antibodies - 250 U 3/10/23 - C Reactive - 13.5, ESR - 39, Vitamin D - 11 7/28/23 - C Reactive 32.9, ESR 97
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- prednisone, steroids, seafood, dairy, gluten, cherries, pineap
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 12.04.2023
- Impfdatum
- 09.08.2022
- Beginn
- 06.04.2023
- Tage bis Beginn
- 240,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest X-ray abnormal
Exposure to communicable disease
Increased bronchial secretion
Lung opacity
Nausea
Oxygen saturation decreased
SARS-CoV-2 test positive
Vomiting
Symptomtext
Brief Summary of Hospital Stay: (Include Significant Findings and Invasive Procedures) patient is a 19-year-old female with past medical history of Rett syndrome, asthma, GERD and chronic tube feeding. She presented for chief complaint of increased pulmonary secretions and vomiting. Patient had been tested positive on home testing for COVID earlier that day after being exposed to a sick family member. On presentation vitals are notable for temperature 100.1?. Labs notable for positive COVID test. Chest x-ray was notable for bilateral perihilar opacities. Patient was admitted initially satting well on room air but had desaturations later in her stay and was therefore started on remdesivir and Decadron for treatment of COVID. Patient required aggressive pulmonary hygiene throughout her stay. Nausea vomiting and increased secretions improved and patient was restarted back on to work home tube feeding formula. Patient was weaned off oxygen requirements and will be discharged home under the care of her mother
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- 3,0
- Labordaten
- COVID positive PCR 4/6/2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 28.07.2022
- Beginn
- 15.10.2022
- Tage bis Beginn
- 79,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness postural
Head discomfort
Magnetic resonance imaging normal
Tinnitus
Symptomtext
So the symptoms were the feelings of dizziness when bending over or exercising and when moving from side to side in addition a feeling of fullness in the head, then I started with ringing in my right ear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness postural
- Hospital-Tage
- -
- Labordaten
- MRI; results were normal blood profile normal results. An ENT did a full exam with no results either. A recommendation was made of either hypertension and a recommendation to a neurologist my PCP also recommended it.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mitral valve prolapse; Thalassemia
- Andere Medikamente
- Vitamin D
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 28.07.2022
- Beginn
- 07.11.2022
- Tage bis Beginn
- 102,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Feeling abnormal
Nasopharyngitis
Oxygen saturation decreased
Pain
Rhinorrhoea
SARS-CoV-2 test positive
Sinusitis
Symptomtext
I felt bad for about a day after receiving the vaccine. I did not have symptoms prior to testing positive for COVID-19. I tested positive for COVID-19 on 11/07/2022. I contacted my doctor, and she did not recommend taking PAXLOVID. I also talked to my daughter-in-law who is a doctor, and she did not recommend PAXLOVID either. My nose was really runny, I had body aches, no nausea and no sore throat. One day my oxygen level was below normal. I treated my symptoms like it was cold. Lots of rest and fluids. About a couple of weeks later, I developed a sinus infection. I went to an urgent care center, and I was given an antibiotic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- 07NOV2022 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Ocular Rosacea; Arthritis
- Andere Medikamente
- ADVIL; estradiol; doxycycline; vitamin B12
- Allergien
- Sulfa; azithromycin
- Vorherige Impfungen
- Second Shingles vaccine June 2021 and Tdap in fall of 20212, both made me really sick like I had the flu.
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 31.01.2023
- Impfdatum
- 27.01.2022
- Beginn
- 01.01.2023
- Tage bis Beginn
- 339,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Bronchospasm
Cardiopulmonary bypass
Human metapneumovirus test positive
Influenza virus test negative
Malaise
SARS-CoV-2 test negative
Symptomtext
I got Covid again December 28th, I was given PAXLOVID. I had just gotten over it and I started getting sick on the 19th of January. My upper respiratory felt like I was getting Covid again but tested negative. I went to the ER, and I had bronchi's spasm really bad. A nurse came and put me in the resuscitation room, and I don't remember much after that. I was on bypass and respiratory support as well as breathing treatments. After that I was discharged on Sunday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 4,0
- Labordaten
- 25JAN23 Human Metapneumovirus positive, 25JAN23 COVID 19 test negative, 25JAN23 Flu swab negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Osteoporosis; Addison's; Chronic Pain; High Blood Pressure; High Cholesterol; Osteoarthritis; Type 2 Diabetes
- Andere Medikamente
- Ropinirole; rosuvastatin; JANUVIA.; PROLIA; ibazocine; meloxicam; metoprolol; montelukast; venlafaxine; hydrocortisone; multivitamin; vitamin D; calcium; XOLAIR; gabapentin; oxycodone; pantoprazole
- Allergien
- Penicillin; sulfa; IV iodinecContrast
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 31.12.2022
- Impfdatum
- 10.08.2022
- Beginn
- 21.12.2022
- Tage bis Beginn
- 133,0
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Vaccination site pain
Symptomtext
Diagnosed with COVID yesterday; Diagnosed with COVID yesterday; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 78-year-old female patient received BNT162b2 (BNT162B2), on 23Feb2021 as dose 1, single (Lot number: EN9581), in right arm, on 23Mar2021 as dose 2, single (Lot number: ER2613), in right arm, on 10Dec2021 as dose 3 (booster), single (Batch/Lot number: unknown), in left arm and on 10Aug2022 as dose 4 (booster), single (Lot number: FP7137) at the age of 77 years, in right arm for covid-19 immunisation; influenza vaccine (FLU [INFLUENZA VACCINE]), on 10Aug2022 as dose number unknown, single (Batch/Lot number: unknown), in left arm for immunisation. The patient's relevant medical history included: "ANA" (unspecified if ongoing), notes: ANA stands for antinuclear antibodies. It means her immune system is about gone. She was diagnosed this past summer in August.; "left branch bundle block diagnosed 12 years ago", start date: 2010 (unspecified if ongoing), notes: left branch bundle block diagnosed 12 years ago.; "heart" (unspecified if ongoing), notes: Indication as Reported by the Primary Source: heart; "supplement" (unspecified if ongoing), notes: Indication as Reported by the Primary Source: supplement. Concomitant medication(s) included: RANOLAZINE oral taken for cardiac disorder (ongoing); IMMUNETI taken for supplementation therapy. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant) all with onset 21Dec2022, outcome "unknown" and all described as "Diagnosed with COVID yesterday". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (21Dec2022) Positive. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course: The patient had not consumed Paxlovid yet and was calling before she took it. Lot No for third Pfizer vaccine dose was EF2593 or maybe ER2593, handwritten on vaccine card. Additional Information for Other medicines immuneti: it had vitamin c, zinc, vitamin D3, elderberry. It ias an advanced immune defense vitamin. The patient took one tablet of Ranolazine by mouth twice a day when she did not forget it. Start date: been on it for 4 years off and on. She was supposed to take it every day but had not taken it today. Caller did not like taking pills. Vaccination Facility Type: It was not a military facility. The other three vaccines were given in town and the National Guard were giving it and it felt like he hit her bone. Caller doesn't have that much fat on her body. Prior Vaccinations (within 4 weeks): Received Flu shot on same date as COVID vaccine on 10Aug2022. The patient did not go to physician's office. There was a product complaint to report. ANA stands for antinuclear antibodies. It means her immune system is about gone. She was diagnosed this past summer in August. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221221; Test Name: COVID test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: ANA; Heart disorder (Indication as Reported by the Primary Source: heart); Left bundle branch block (left branch bundle block diagnosed 12 years ago.); Supplementation therapy (Indication as Reported by the Primary Source: supplement)
- Andere Medikamente
- RANOLAZINE; IMMUNETI
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 17.11.2022
- Impfdatum
- 17.08.2022
- Beginn
- 30.10.2022
- Tage bis Beginn
- 74,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anosmia
COVID-19
Chest X-ray
Chills
Cough
Electrocardiogram
Fatigue
Headache
Hypoxia
Myalgia
Nausea
Pyrexia
SARS-CoV-2 test positive
Symptomtext
COVID-19 symptoms; headache; coughing; fever; chills; lost sense of smell, nausea; muscle aches; fatigue. Also my oxygen levels was 80 I was admitted for Hypoxia and was given infusions of remdesivir and erythromycin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- 1,0
- Labordaten
- COVID-19 10/30/2022 positive; chest x-ray; EKG.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hyperlipidemia
- Andere Medikamente
- Vitamin D tablets; rosuvastatin; fish oil; latanoprost eye drops; fluticasone.
- Allergien
- Lisinopril; seasonal allergies
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 10.11.2022
- Impfdatum
- 10.08.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 52,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Headache
Myalgia
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
I had a sore throat, dry cough, very tired, muscle aches everywhere, headache. and did not have a fever. I tested positive at home for COVID-19. I called my doctor on 10/02/2022 because I figured since I am 68 that I should get PAXLOVID, which I was prescribed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test, positive, 10/02/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Osteoporosis; Arthritis; Depression
- Andere Medikamente
- Modafinil; gabapentin; escitalopram; multivitamin; calcium; vitamin D; alendronate
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 10.11.2022
- Impfdatum
- 09.11.2021
- Beginn
- 15.07.2022
- Tage bis Beginn
- 248,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
COVID-19
Chills
Dry throat
Feeling abnormal
Headache
Illness
Myalgia
Nasal discomfort
Nasal inflammation
Neck pain
Night sweats
Ocular discomfort
Oropharyngeal pain
Quarantine
Rhinalgia
SARS-CoV-2 test positive
Sneezing
Symptomtext
I was having a sore throat it was dry scratchy and weird. It lasted all day and that evening I took a home COVID-19 test, and it was positive. I had a brain fog and muscle aches in my head neck and shoulders. From the 15th through the 22nd I had postnasal drip, a headache with pressure behind my eyes, I was sneezing, I had chills and night sweats, my nasal passages were inflamed painful and burning, I also had the worst of it all through the 17th but from then on, I felt better and better each day. I really just quarantined and stayed home, stayed hydrated, and slept and I felt that it was just a horrible sickness, and I was really sick.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Biotin; vitamin C; probiotic
- Allergien
- FLAGYL
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 28.10.2022
- Impfdatum
- 09.03.2021
- Beginn
- 26.10.2022
- Tage bis Beginn
- 596,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Computerised tomogram thorax abnormal
Lung consolidation
Respiratory viral panel
SARS-CoV-2 test
Sputum culture
COVID-19
Malaise
Vaccine breakthrough infection
Symptomtext
Patient hospitalized and had breakthrough COVID-19 that was symptomatic
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 27.10.2022
- Impfdatum
- -
- Beginn
- 08.08.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Malaise
SARS-CoV-2 test positive
Symptomtext
While on vacation didn't feel well so we wanted to test to make sure. Tested on the 23 after a vacation and the results were positive. Then we contacted our doctor told her what issues we had, and I was given antibiotics and it all cleared up in a few days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- None
- Andere Medikamente
- Levothyroxine
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 06.10.2022
- Impfdatum
- 03.10.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain
Wrong product administered
Symptomtext
WAS CONSENTED TO RECEIVE A BOOSTER, ALTHOUGH BOOSTERS ARE NO LONGER BEING GIVEN. THEN RECEIVED BOOSTER COVID-19 VACCINE. DID RECEIVE A STANDING ORDER OF TYLENOL 350MG TWO TABS PO X 1 DOSE DUE TO REPORTING POST VACCINATION PAIN. NO FURTHER ADVERSE SIGNS OR SYMPTOMS WERE NOTED OR REPORTED. STAFF WAS RE-EDUCATED THAT BOOSTERS ARE NO LONGER GIVEN AT THE FACILITY.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- NONE AT THIS TIME
- Aktuelle Erkrankungen
- REPORTED A STOMACH ON INITIAL MEDICAL EXAM ON 10/03/2022 PRIOR TO VACCINE ADMINISTRATION
- Vorgeschichte
- NONE REPORTED
- Andere Medikamente
- NONE
- Allergien
- SHELLFISH
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Nausea
Pallor
Visual impairment
Symptomtext
At approximately 1543, client received the Pfizer COVID vaccine (LOT# FP7137) at approximately 1543. At approximately 1548, client's father alerted RN. Client's father reported that client "saw black" and felt like vomiting. RNs assisted client into anti-gravity chair. RN noted palor and diaphoresis. Client denied itchiness, difficulty swallowing and difficulty breathing. Client's father reported no similar history and reported that client was anxious before vaccination. RNs recommended client to stay for 30 minutes for observation. At 1548, RNs assessed client: blood pressure 112/64 mmHg, heart rate 110 bpm, SpO2 98%, and respiratory rate 16 breaths/min. RNs placed a cool wash cloth on client's forehead and water to drink. At 1603, RNs reassessed client: 117/64 mmHg, heart rate 96 bpm, SpO2 98%, respiratory rate 16 breaths/min, and client reported feeling better. At 1603, client denied previous symptoms. At 1620, RN reassessed client. Client denied previous symptoms. RN educated client and client's father on signs/symptoms of when to seek emergency care and to sign up on V-safe. At 1621, client left facility with unlabored respirations and steady gait with father.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- None reported
- Allergien
- None reported
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- 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: ja
Erholt: nein
Dizziness
Symptomtext
This is reported by the nurse who gave him the vaccine, he got his vaccine and his only complaint was dizziness. The patient was transferred to the ER for FU. He is just being monitored. His VS were really good, the only complaint was dizziness. He was doing fine while being transported to the ER. Mother reports he has never had a reaction to vaccines in the past.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Eggs.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 13.08.2022
- Beginn
- 13.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Product administered to patient of inappropriate age
Somnolence
Symptomtext
My son was given the adult vaccine instead. I was called on August 19, 2022 to verify his birthdate, I did. A couple of hours later I received another call about his birthdate so, I asked what was going on. I was then asked how my son was doing and if I'd noticed any side effects. His arm was sore but, I did notice that he was extra sleepy that afternoon of the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Na
- Aktuelle Erkrankungen
- Na
- Vorgeschichte
- NA
- Andere Medikamente
- Concerta
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 15.09.2022
- Impfdatum
- 09.09.2022
- Beginn
- 13.09.2022
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Ecchymosis
Epstein-Barr virus antibody negative
Epstein-Barr virus antibody positive
Fatigue
Full blood count normal
International normalised ratio normal
Laboratory test abnormal
Metabolic function test normal
Oropharyngeal pain
Prothrombin time normal
Red blood cell sedimentation rate normal
Symptomtext
Patient came to the office on 9/13 with her mother who was concerned that she had multiple areas of bruising to her anterior thighs that started on 9/10 (the day following her vaccine on 9/9). She also reported fatigue. On 9/14 she came to the office again for recheck and had a few more areas of ecchymosis to anterior thighs and complained of sore throat and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- CBC, CMP, sed rate, PT/INR, EBV titers. All labs unremarkable other than EBV titers which results revealed suggestive of past EBV infection. (IGG positive in the EBV titers, IGM normal value)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- asthma, ADHD
- Andere Medikamente
- Methylphenidate HCL 50mg once daily, Omeprazole 40mg daily PRN, Albuterol inhaler PRN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 14.09.2022
- Impfdatum
- 16.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Myalgia
Pain
Symptomtext
Severe left arm muscle and joint pain. Painful with movement and extension. Some minor aches in all extremities that does not go away unless I take ibuprofen or tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- caught Covid at the end of July and tested positive July 24th. Did notify patient at time of vaccination, she informed me it was ok for me to receive Pfizer booster.
- Vorgeschichte
- DM type 2
- Andere Medikamente
- prenatal vitamins, omeprazole
- Allergien
- tramadol, metformin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 06.09.2022
- Impfdatum
- 06.09.2022
- Beginn
- 06.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blood glucose
Dizziness
Visual impairment
Symptomtext
Patient received vaccine and while waiting the recommended 15 minutes, patient's father stated patient started to experience dizziness, light headedness, and was "seeing stars". Father also noted the patient was feeling weak while having patient grip his hand. EMS was called and arrived at roughly 6:00 pm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None, EMS completed blood glucose and pulse ox, results were not shared with the pharmacist
- Aktuelle Erkrankungen
- None reported by father
- Vorgeschichte
- None reported by father
- Andere Medikamente
- None reported by father
- Allergien
- None reported by father
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 02.09.2022
- Impfdatum
- 10.08.2022
- Beginn
- 11.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Pyrexia
Symptomtext
Myalgia & Fever Narrative:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 24.08.2022
- Beginn
- 24.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Fatigue
Headache
Symptomtext
Narrative: Headache, Arthralgia, Fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Axillary pain
Oedema peripheral
Symptomtext
Armpit swelling and pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 01.09.2022
- Impfdatum
- 29.08.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash erythematous
Skin warm
Symptomtext
Red rash, hot to touch, itchy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 30.08.2022
- Impfdatum
- 25.08.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- 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
Systemic: Redness, swelling and heat below injection site above elbow-Mild.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 28.08.2022
- Impfdatum
- 23.08.2022
- Beginn
- 23.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site swelling
Lymphadenopathy
Symptomtext
Site: Pain at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Lymph Node Swelling-Medium, Additional Details: Patient has lymph node swelling and was concerned
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.08.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A patient (no qualifiers provided) received BNT162b2 (BNT162B2), as dose 3 (booster), single (Lot number: FP7137), in right deltoid for covid-19 immunisation; influenza vaccine (FLU), as dose number unknown, single (Batch/Lot number: unknown), in right deltoid. The patient's relevant medical history and concomitant medications were not reported. Vaccination history included: Covid-19 vaccine (Primary immunization series completed, unknown manufacturer.), for Covid-19 immunization. The following information was reported: PAIN IN EXTREMITY (non-serious), outcome "unknown", described as "he arm is so painful and it is very uncomfortable". Additional information: The received Booster (reported as yesterday) and also Flu shot (unspecified Flu shot) in my right deltoid and the have been up all night, the arm was so painful and it was very uncomfortable. Additional Context: Concern, consumer stated, "This was not an emergency by any means but the patient received the Booster yesterday evening about 6 O'clock in (State withheld) at (name withheld) and the patient was also given the Flu shot (unspecified Flu shot). They were given in my right deltoid and the patient have been up all night. The patient was just, the arm was so painful, the just want to know if the patient can take some sort of (treatment) to relieve some of that.". Consumer stated, "It is just very uncomfortable. I just wanted to know if I could take like a Motrin or something to get some relief from that." In response consumer stated, "Well that won't help me." Response was provided, consumer was informed to visit to nearest Emergency room in case of emergency. In response consumer stated, "Well they are not going to because it is Sunday and nobody is going to tell me until tomorrow morning. Thank you anyway." In response consumer stated, "Well they are not going to because it is Sunday and nobody is going to tell me until tomorrow morning. Thank you anyway." No follow-up attempts are possible. No further information is expected. Sender's Comments:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 25.08.2022
- Impfdatum
- 23.08.2022
- Beginn
- 24.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Diarrhoea
Fatigue
Headache
Injection site pain
Myalgia
Nausea
Pain
Tinnitus
Symptomtext
August 24 side effects: Extreme tiredness, achy all over body, injection site pain, tinnitus (ringing of ears), headache, nausea, muscle pain, joint pain and chills. These were throughout the day. August 25 side effects: Diarrhea in morning. It seemed like I had more severe side effects with 4th shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- GERD, osteoporosis, generalized anxiety
- Vorgeschichte
- GERD, osteoporosis, generalized anxiety
- Andere Medikamente
- Metoprolol Succinate 25mg, Paroxetine HCl, Multivitamin/Multimineral, Vitamin D3 1,000IU 25mcg, Vitamin E, D alpha-tocopherol acetate
- Allergien
- Clindamycin, Erythromycin, Penicillin, acidic foods, oranges, coffee
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 24.08.2022
- Impfdatum
- 20.08.2022
- Beginn
- 20.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Back pain
Diarrhoea
Fatigue
Hypersomnia
Influenza like illness
Memory impairment
Muscle spasms
Neck pain
Pain in extremity
Symptomtext
He got his vaccine, he got real tired, and came down with flu-like symptoms to the extreme. He had pain from his elbow to his shoulders, neck, upper back achy in nature. He wasn't nauseated, but he had some cramps and then he had diarrhea. It knocked him out, he slept through Sunday, he does recall anything about Sunday, slept for 24 hours. On Monday he was feeling weak, but cramps had gone away. The aching has also eased up within the next couple of days and is gone now. He has never had a reaction this bad before. He had both Moderna vaccines, and only had a reaction for about a 1/2 a day, and this is the worst one he ever had. He did not take anything for it, he just slept.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypertension.
- Andere Medikamente
- BP medicine.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 24.08.2022
- Impfdatum
- 24.07.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site haemorrhage
Injection site reaction
Myalgia
Symptomtext
No peritherapeutic pain. Ecchymosis at injection site onset within 24 h, resolved after 18 days. Myalgia at injection site onset within 24 h and continuing to the present (30 days later): tolerable but non negligible upon exertion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site haemorrhage
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Trazadone, Montelukast, vitamins D and C, magnesium
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 22.08.2022
- Impfdatum
- 22.08.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Emotional disorder
Hyperhidrosis
Immediate post-injection reaction
Panic attack
Symptomtext
Immediately following injection of Pfizer vaccine patient had a panic attack due to emotional response. No allergic reaction was noted. Patient was sweaty, light headed, dizzy and felt faint. Patient never lost consciousness. Patient asked for ambulance to go to hospital to be examined. Patient left in the care of emergency personel.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Anxiety and panic disorder
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 21.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Gingival pain
Toothache
Urticaria
Symptomtext
Patient verbalizes that 3 days after being inoculated a pain begins in the gum and teeth and on the 4th day hives came out in the arms and right armpit and lower legs and buttocks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Gingival pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- High pressure, Neuropathy
- Vorgeschichte
- -
- Andere Medikamente
- Plavix, Gabapentin 100mg, Rosubastatin 20mg, Lozartan 100mg.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 21.08.2022
- Impfdatum
- 08.08.2022
- Beginn
- 09.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
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
- NM
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 21.08.2022
- Impfdatum
- 15.08.2022
- Beginn
- 16.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Symptomtext
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
- PA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 19.08.2022
- Impfdatum
- 19.08.2022
- Beginn
- 19.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Nausea
Vomiting
Symptomtext
Pt felt nauseous and lowered her head. she them vomited into a trash can. she was provided with a cold pack for the back of her neck. pt felt better a short while later. She stated that she gets nervous around needles. She failed to dislose this prior to receiving the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE KNOWN
- Allergien
- NKA
- Vorherige Impfungen
- pt stated she gets nervous around needles
- Staat
- VA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 19.08.2022
- Impfdatum
- 17.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphonia
Oesophageal motility disorder
Oropharyngeal pain
Speech disorder
Symptomtext
Patient reported on 08-19-22 8:00pm that he lost his voice 1 hour after received the COVID dose 2 vaccine on 08-17-22 at 5:15pm.. He has had difficulty talking and sore throat after vaccine administration. Patient has current health condition of esophageal dysmotility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 18.08.2022
- Impfdatum
- 18.08.2022
- Beginn
- 18.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Disorientation
Dizziness
Pallor
Peripheral coldness
Symptomtext
Administered Pfizer dose in left arm and had patient wait for 15 minutes. Patient started to complain of feeling faint and seemed disoriented. We gave patient some cold water. We moved him to a cooler area in the pharmacy, then his hands started to lose all color and became very cold. We called 911 for further assistance. They arrived soon after. This situation was approximately over 30-45 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 17.08.2022
- Impfdatum
- 12.08.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Pyrexia
Rash
Rash erythematous
Symptomtext
Fever the night of vaccination administration noted red flat rash on palms. Fever better after 48, rash slightly better now, still burns
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- History of Kawasaki
- Andere Medikamente
- NA
- Allergien
- Allery test positive for weeds and trees
- Vorherige Impfungen
- -
- Staat
- DE
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 17.08.2022
- Impfdatum
- 16.08.2022
- Beginn
- 16.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Feeling cold
Feeling hot
Headache
Insomnia
Malaise
Muscle spasms
Night sweats
Pyrexia
SARS-CoV-2 test negative
Symptomtext
Took Janssen shot back in 05/15/2021, got the shot around 10am and by 11pm all the feelings of covid were present. Took pfizer at 11:30 on 08/16/2022, something happened. By 9pm that same night all symptoms of covid had been present. Throughout both nights, there was lack of sleep, muscle spasms, headache, night sweats, fever, cold chills, and feeling of burning up. Both times told no one had issues with each shot. Yet in these 2 cases, both times felt as if covid had taken over. Even though negative for covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- IBS
- Vorgeschichte
- IBS
- Andere Medikamente
- -
- Allergien
- Penicillin, areithomicin, ceclore, amoxocilin, dairy
- Vorherige Impfungen
- Age 30, vaccination date 05/15/2021, vaccine type Janssen Z05A21A, described as same as the Pfizer shot.
- Staat
- MA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 17.08.2022
- Impfdatum
- 12.08.2022
- Beginn
- 13.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Chills
Dizziness
Fatigue
Headache
Lethargy
Nausea
Pain
Flushing
Hyperhidrosis
Pyrexia
Symptomtext
Systemic: Body Aches Generalized-Severe, Systemic: Chills-Severe, Systemic: Dizziness/Lightheadedness-Severe, Systemic: Exhaustion/Lethargy-Severe, Systemic: Fever-Severe, Systemic: Flushed/Sweating-Severe, Systemic: Headache-Severe, Systemic: Joint Pain-Severe, Systemic: Weakness-Severe, Additional Details: Patient had these same symptoms following second COVID-19 Pfizer vaccination as well. Symptoms lasted 3 days after second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Patient had these same symptoms following second COVID-19 Pfizer vaccination as well. Symptoms lasted 3 days after second dose.
- Staat
- OH
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 16.08.2022
- Impfdatum
- 09.08.2022
- Beginn
- 09.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Headache
Pain
Pain in extremity
Symptomtext
Severe body aches; joing pain; shivering, couldn't get warm; arm pain; severe headache; This is a spontaneous report received from a contactable reporter(s) (Other HCP). The reporter is the patient. A 55-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 09Aug2022 at 10:00 as dose 4 (booster), single (Lot number: FP7137) at the age of 54 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Coeliac disease" (unspecified if ongoing); "Gluten allergy" (unspecified if ongoing). The patient's concomitant medications were not reported. Vaccination history included: BNT162b2 (Dose number=3, lot number: FE3590, administration time: 12:00 PM, Left arm), administration date: 28Oct2021, when the patient was 54-year-old, for Covid-19 immunization, reaction(s): "Severe body aches", "Joint pain", "Shivering", "Pain in arm", "Headache"; BNT162b2 (Dose 2, lot number: EL1284), administration date: 13Jan2021, when the patient was 53-year-old, for Covid-19 immunization, reaction(s): "Severe body aches", "Joint pain", "Shivering", "Pain in arm", "Headache"; BNT162b2 (Dose 1, lot number: EJ1685), administration date: 23Dec2020, when the patient was 53-year-old, for Covid-19 immunization, reaction(s): "Severe body aches", "Joint pain", "Shivering", "Pain in arm", "Headache". The following information was reported: PAIN (non-serious) with onset 09Aug2022 at 20:00, outcome "recovering", described as "Severe body aches"; PAIN IN EXTREMITY (non-serious) with onset 09Aug2022 at 20:00, outcome "recovering", described as "arm pain"; ARTHRALGIA (non-serious) with onset 09Aug2022 at 20:00, outcome "recovering", described as "joing pain"; HEADACHE (non-serious) with onset 09Aug2022 at 20:00, outcome "recovering", described as "severe headache"; CHILLS (non-serious) with onset 09Aug2022 at 20:00, outcome "recovering", described as "shivering, couldn't get warm".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Celiac disease; Gluten intolerance
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 15.08.2022
- Impfdatum
- 09.08.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Axillary mass
Headache
Tenderness
Symptomtext
I developed a golf ball sized lump under my left arm pit the night after I received the vaccine which was tender and pain if I pressed on it. I developed headaches as well. I visited my doctor on 8/11. No treatment or test were provided but I was told to ice the lump. The lump is still there though smaller, the size of a quarter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes, High Blood Pressure
- Andere Medikamente
- Tylenol; Vitamin D3; Prenjority; Amlodipine; Losartan; Prilosec; Synthroid
- Allergien
- Biotin; Carvedilol
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 14.08.2022
- Impfdatum
- 05.08.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Joint range of motion decreased
Pain in extremity
Symptomtext
I had a pain in my right leg behind my knee. I could not bend that leg and almost wondered if it was a blood clot. After 30ish minutes or so it vanished. I had never felt anything like that before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 12.08.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Pain in extremity
Tinnitus
Symptomtext
Patient reported feeling dizziness, having ringing in her ears and sweating 3 minutes after vaccination. She also reported having pain in her arm. She was given water and cool rag to help cool her down. She also reported not eating since 2pm today so she drank some orange juice and crackers. After 15 minutes she was feeling better and was able to leave on her own/
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- none reported
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 11.08.2022
- Impfdatum
- 06.08.2022
- Beginn
- 07.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Urticaria
Symptomtext
severe hives everywhere on my body. Currently taking 2 Benadryl every for hrs and pepcid 40mg a day + hydroxyzine 3x a day + prednisone
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UTI
- Vorgeschichte
- No
- Andere Medikamente
- Yasmin
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 7,0
- Geschlecht
- F
- Eingang
- 10.08.2022
- Impfdatum
- 10.08.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LL
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Myalgia
No adverse event
Product preparation issue
Pyrexia
Swelling
Symptomtext
Intern failed to dilute vaccine prior to administration, resulting in the child receiving 0.2 mL of undiluted vaccine. After discovery of incident patient's guardian was contacted and told to look out for local and system side effects such as muscle soreness, swelling, and fever. Thus far, patient has not reported any adverse events to event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 10.08.2022
- Impfdatum
- 05.08.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye pain
Facial pain
Injection site pain
Injection site swelling
Jaw clicking
Lip pain
Pain in jaw
Rash
Rash erythematous
Rash papular
Rash pruritic
Symptomtext
I received my injection in my left arm and had pain and swelling at the injection site, but I also experienced pain from my jaw through the left side of my face. The left side of my lip up into my eye was all in pain. When I woke up the next morning, I could feel pain all in that area and it felt like my jaw was set to the right. I heard a cracking sound at some point. When I was eating that morning, I felt a crack and it felt like my jaw shattered. I'm still feeling pain in my face, and it looks asymmetrical. I took a picture. I also developed a red rash on both legs from above my knees and up into my thighs. About 7 inches above my knee, I have been seeing red spots and itchy patches that have been raised. I was taking over the counter non drowsy allergy medication because I was already experiencing some allergy issues, yet I was still seeing the rash on my legs. I went to the doctor who gave me a shot of MEDROL and prescribed prednisone for 10 days and advised that I continue taking BENADRYL and non-drowsy allergy medication and come back in two weeks, unless things get worse, in which case he wants to see me immediately. I have also been experiencing an itching sensation all over in random places.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pain
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Fibromyalgia; IBF; IC; Gastritis; Acid Reflux; Asthma; ESL; Restless leg syndrome; Dry eyes and mouth; Thyroid issues; Depression; BPI; Over active bladder.
- Andere Medikamente
- Levothyroxine; gabapentin; hydroxychloroquine; duloxetine; trazadone; women's ONE A DAY; biotin; prebiotic; probiotic; aspirin; vitamin B3; valacyclovir; famotidine; chewable CREON vitamin; IBGUARD; albuterol inhaler; allergy shot; biotin;
- Allergien
- Morphine; codeine.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 08.08.2022
- Impfdatum
- 29.07.2022
- Beginn
- 31.07.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test negative
Symptomtext
This was my second booster and have had side effects for 9 days - fever, headache, sore throat (gone now but 2 days)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 4 at home covid tests and one pcr to confirm covid negative
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- daily supplements - zinc, fish oil, b vitamins
- Allergien
- none
- Vorherige Impfungen
- shingles first dose - 52 yrs old
- Staat
- NY
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 08.08.2022
- Impfdatum
- 04.08.2022
- Beginn
- 04.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Headache
Symptomtext
Chills, Headache, Weakness Temperature of 99 F
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 6,0
- Geschlecht
- F
- Eingang
- 07.08.2022
- Impfdatum
- 05.08.2022
- Beginn
- 07.08.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Pyrexia
Symptomtext
Fever (101 degrees), fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Fatigue
- Staat
- NM
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 03.08.2022
- Impfdatum
- 28.07.2022
- Beginn
- 28.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Diarrhoea
Headache
Injection site bruising
Injection site erythema
Injection site pain
Injection site swelling
Nausea
Pain
Pyrexia
Symptomtext
Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Diarrhea-Medium, Systemic: Fever-Severe, Systemic: Headache-Medium, Systemic: Nausea-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Eye pruritus
Hypoaesthesia oral
Pruritus
Symptomtext
35 years old women, after the Pfizer vaccine she complain to the paramedic in the observation that she was feeling itchy in her trout and eye. At this moment the paramedic pass the patient to the triage zone, paramedic took the vitals: BP:130/85, HR:105, Temperature: 36.6C and dextro 113. The patient report feeling numbness in her tongue and we give 25mg of Benadryl. We observed the patient for 30 minutes and we retake the vitals: BP: 130/865, HR 90 SO2:98.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- NO
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- NO
- Allergien
- Demerol solumedrol yodo
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Ear pain
Headache
Hypoaesthesia
Muscle spasms
Oropharyngeal pain
Pain
Pain in extremity
Pyrexia
Respiratory tract congestion
Rhinorrhoea
Sneezing
Symptomtext
Night of the vaccine: had some pains in my foot, light but sharp shooting pains / cramping sensation on top of feet; had a headache, began having body aches. Morning after the vaccine: entire body ached, headache, sneezing / runny nose, tired. Mid-morning after the vaccine: Body aches, chills, fever, dizziness, headache, nauseous, slight congestion and sore throat, numbness in hands, sharp pain on entire right side of head /ear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Levoxyl 112 mcg, Levothyronine 10 mg, Women's Daily Vitamin
- Allergien
- N/A
- Vorherige Impfungen
- 1st dose of Pfizer covid-19 vaccine - light-headedness, body weakness, slight body aches
- Staat
- -
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 28.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Diarrhoea
Pain
Vomiting
Symptomtext
patient described vomiting and diarrhea the morning after injection followed by body aches and chills that lasted until the next morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 01.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pain in extremity
Product administered at inappropriate site
Symptomtext
Vaccination was given too low by technician. Patient was complaining of arm pain and pain shooting down her arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- None that we know of
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 31.07.2022
- Impfdatum
- 31.07.2022
- Beginn
- 31.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Flushing
Muscle rigidity
Muscle spasms
Muscle tightness
Musculoskeletal stiffness
Myalgia
Symptomtext
patient experienced flushing, and hand muscle cramps and rigity also experienced tightness in calf muscles. After patient sat down for about 15 minutes minutes and hydrated, the patient felt better and the muscle stiffness went away except for soreness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 25.07.2022
- Beginn
- 25.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Oropharyngeal pain
Swollen tongue
Symptomtext
After receiving the vaccine, the patient waited for 30 minutes in front of the pharmacy. After 30 minutes the patient walked up to the pharmacy's counseling window and told me that she was experiencing sore throat and her tongue was swollen. I immediately, call for the store's management to head to the pharmacy and administer 10 mL of benadryl to the patient orally. Explained to the patient that both her and I will be sitting down for another 30 minutes to make sure the symptoms don't progress. After 25 minutes the patient said her symptoms were getting better. I followed up with her the next day and she said she feels much better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- n/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 28.12.2023
- Impfdatum
- 28.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a Consumer or other non HCP. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Jul2022 as dose 4 (booster), single (Lot number: FP7137) at the age of 61 years for covid-19 immunisation; COVID-19 vaccine (COVID-19 VACCINE), as dose 1, single), as dose 2, single) and as dose 3 (booster), single) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. Past drug history included: Doxycycline, reaction(s): "Known allergies: doxycycline"; Rhondomycin, reaction(s): "Known allergies: Rondomycin". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "not recovered" and all described as "COVID 19 Treatment". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical information: Patient received Paxlovid (Lot Number: GJ7330) from 12Dec2023 to 17Dec2023, for the treatment of COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 06.10.2023
- Impfdatum
- 09.03.2023
- Beginn
- 09.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS RECEIVED PAST THE BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 06.10.2023
- Impfdatum
- 16.03.2023
- Beginn
- 16.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
VACCINE WAS RECEIVED PAST THE BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 06.10.2023
- Impfdatum
- 09.03.2023
- Beginn
- 09.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS RECEIVED PAST THE BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 06.10.2023
- Impfdatum
- 16.03.2023
- Beginn
- 16.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS RECEIVED PAST THE BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 06.10.2023
- Impfdatum
- 09.03.2023
- Beginn
- 09.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS RECEIVED PAST THE BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- NONE
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 06.10.2023
- Impfdatum
- 16.03.2023
- Beginn
- 16.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS RECEIVED PAST THE BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 06.10.2023
- Impfdatum
- 09.03.2023
- Beginn
- 09.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS RECEIVED PAST THE BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 06.10.2023
- Impfdatum
- 16.03.2023
- Beginn
- 16.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS RECEIVED PAST THE BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- NONE
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 06.10.2023
- Impfdatum
- 20.03.2023
- Beginn
- 20.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS RECEIVED PAST THE BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 06.10.2023
- Impfdatum
- 09.03.2023
- Beginn
- 09.03.2023
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS RECEIVED PAST THE BEYOND USE DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- -
- Geschlecht
- F
- Eingang
- 14.06.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Hypersensitivity
SARS-CoV-2 test
Symptomtext
Was never allergic to anything until I got these vaccinations now I'm allergic to everything; This is a spontaneous report received from contactable reporter(s) (Other HCP). The reporter is the patient. A 58-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), as dose 1, single (Lot number: FP7137) for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: HYPERSENSITIVITY (disability, life threatening), outcome "not recovered", described as "Was never allergic to anything until I got these vaccinations now I'm allergic to everything". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Unknown Results, notes: If covid tested post vaccination: Yes/Nasal Swab.; Sender's Comments: Based on known drug safety profile, there is reasonable possibility of causal association between the event (HYPERSENSITIVITY) and BNT162B2. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to regulatory authorities, Ethics Committees, and Investigators, as appropriate.,Linked Report(s) : US-PFIZER INC-202300218333 same reporter/patient/drug, different dose/event;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypersensitivity
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid; Result Unstructured Data: Test Result:Unknown Results; Comments: If covid tested post vaccination: Yes/Nasal Swab
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 24.05.2023
- Impfdatum
- 17.08.2022
- Beginn
- 29.09.2022
- Tage bis Beginn
- 43,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines Pfizer 3/2/21 Lot# EN6198; Pfizer 3/23/21 Lot# EN6208; Pfizer 10/22/21 lot# FF2590; Pfizer 8/17/22 lot# FP7137
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 11.05.2023
- Impfdatum
- 11.08.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 28,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chronic respiratory failure
Left ventricular failure
Respiratory failure
Symptomtext
CHRONIC HYPOXEMIC RESPIRATORY FAILURE 9/12/2022 DIASTOLIC HEART FAILURE, UNSPECIFIED ACUITY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chronic respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 05.05.2023
- Impfdatum
- 22.08.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 40,0
- Dosis
- N/A
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Laboratory test abnormal
Maculopathy
Photopsia
Visual field defect
Symptomtext
I began to see flashes in both eyes early October 2022 which began going away a couple weeks into October 2022. In place of the flashes I began to develop grey spots that occlude central vision partially. I still have this issue as of typing this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Laboratory test abnormal
- Hospital-Tage
- -
- Labordaten
- I have had vision tests which found slight abnormalities to my macula of both eyes.
- Aktuelle Erkrankungen
- Broken Toe
- Vorgeschichte
- None
- Andere Medikamente
- Vitafusion Gummy Multivitamins Elderberry Gummy Multivitamins Multicollagen Protein Supplement
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 12.04.2023
- Impfdatum
- 20.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
Vaccination Failure; COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 68-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 04May2021 as dose 1, single (Lot number: ER8736), in left arm, on 26May2021 as dose 2, single (Lot number: EW0172), in left arm, on 03Jan2022 as dose 3 (booster), single (Lot number: 33025BO), in left arm and on 20Aug2022 as dose 4 (booster), single (Lot number: Fp7137) at the age of 67 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Asthma" (unspecified if ongoing); "SLE" (unspecified if ongoing); "Liver Steatosis" (unspecified if ongoing); "Atherosclerosis" (unspecified if ongoing). The patient's concomitant medications were not reported. The following information was reported: VACCINATION FAILURE (medically significant), outcome "unknown"; COVID-19 (medically significant), outcome "unknown". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) Postive, notes: COVID 19 Treatment; (03Apr2023) Negative, notes: tested neg x2(Mon & Thurs); (06Apr2023) Negative, notes: tested neg x2(Mon & Thurs); (08Apr2023) Positive, notes: I have tested positive for covid. Therapeutic measures were taken as a result of vaccination failure, covid-19.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300148525 same patient, different drug/event (Paxlovid);
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID 19 Test; Result Unstructured Data: Test Result:Postive; Comments: COVID 19 Treatment; Test Date: 20230403; Test Name: COVID-19 virus test; Test Result: Negative ; Comments: tested neg x2(Mon & Thurs).; Test Date: 20230406; Test Name: COVID-19 virus test; Test Result: Negative ; Comments: tested neg x2(Mon & Thurs).; Test Date: 20230408; Test Name: COVID-19 virus test; Test Result: Positive ; Comments: I have tested positive for covid
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Asthma; Atherosclerosis; SLE; Steatosis hepatic
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 27.03.2023
- Impfdatum
- 21.03.2023
- Beginn
- 27.03.2023
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient did not have an adverse reaction but vaccine was given too soon after 2nd Covid-19 vaccine; was given 1 month after 2nd vaccine dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- Unsure
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 24.03.2023
- Impfdatum
- 06.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 74-year-old male patient received BNT162b2 (BNT162B2), on 06Aug2022 as dose 4 (booster), single (Lot number: fp7137) at the age of 73 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive; Positive, notes: I tested Covid positive after 3 continuous Covid test negative; Negative, notes: I tested Covid positive after 3 continuous Covid test negative; Negative, notes: Tested Covid positive after 3 continuous Covid test negative; Negative, notes: Tested Covid positive after 3 continuous Covid test negative. Therapeutic measures were taken as a result of drug ineffective, covid-19 with Paxlovid from 09Mar2023 to 13Mar2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 Test; Test Result: Positive ; Test Name: Covid-19 Test; Test Result: Positive ; Comments: Tested Covid positive after 3 continuous Covid test negative; Test Name: Covid-19 Test; Test Result: Negative ; Comments: Tested Covid positive after 3 continuous Covid test negative; Test Name: Covid-19 Test; Test Result: Negative ; Comments: Tested Covid positive after 3 continuous Covid test negative; Test Name: Covid-19 Test; Test Result: Negative ; Comments: Tested Covid positive after 3 continuous Covid test negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 08.03.2023
- Impfdatum
- 21.08.2022
- Beginn
- 15.02.2023
- Tage bis Beginn
- 178,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 4 vaccines pfizer 4/13/21 Lot# EW0164; Pfizer 5/3/21 Lot# Ew0172; Pfizer 8/18/21 Lot# FC3180; Pfizer 8/21/22 Lot# FP7137
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 06.03.2023
- Impfdatum
- 29.08.2022
- Beginn
- 23.02.2023
- Tage bis Beginn
- 178,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
SARS-CoV-2 test negative
Upper respiratory tract infection
Symptomtext
I experienced a cough that would not go away when I went to the doctor the diagnosed it as a upper respiratory infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- COVID-19 - Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Kidney disease
- Andere Medikamente
- Hydrochlorothiazide; Levothyroxine; Vitamin B; Adderall; Amitriptyline; Vitamin B12
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Product packaging confusion
Symptomtext
FACILITY BELIEVES THEY GAVE PRIMARY MONOVALENT VACCINE IN ERROR FOR BIVALENT VACCINE. NURSING COULD NOT TELL THE DIFFERENCE BETWEEN THE BOTTLES AND REPORTED THE LOT # FP7137 WAS USED FOR VACCINATION WHICH IS PRIMARY MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
FACILITY BELIEVES THEY GAVE PRIMARY MONOVALENT VACCINE IN ERROR FOR BIVALENT VACCINE. NURSING COULD NOT TELL THE DIFFERENCE BETWEEN THE BOTTLES AND REPORTED THE LOT # FP7137 WAS USED FOR VACCINATION WHICH IS PRIMARY MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
FACILITY BELIEVES THEY GAVE PRIMARY MONOVALENT VACCINE IN ERROR FOR BIVALENT VACCINE. NURSING COULD NOT TELL THE DIFFERENCE BETWEEN THE BOTTLES AND REPORTED THE LOT # FP7137 WAS USED FOR VACCINATION WHICH IS PRIMARY MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Product administration error
Symptomtext
FACILITY BELIEVES THEY GAVE PRIMARY MONOVALENT VACCINE IN ERROR FOR BIVALENT VACCINE. NURSING COULD NOT TELL THE DIFFERENCE BETWEEN THE BOTTLES AND REPORTED THE LOT # FP7137 WAS USED FOR VACCINATION WHICH IS PRIMARY MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Product packaging confusion
Symptomtext
FACILITY BELIEVES THEY GAVE PRIMARY MONOVALENT VACCINE IN ERROR FOR BIVALENT VACCINE. NURSING COULD NOT TELL THE DIFFERENCE BETWEEN THE BOTTLES AND REPORTED THE LOT # FP7137 WAS USED FOR VACCINATION WHICH IS PRIMARY MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
FACILITY BELIEVES THEY GAVE PRIMARY MONOVALENT VACCINE IN ERROR FOR BIVALENT VACCINE. NURSING COULD NOT TELL THE DIFFERENCE BETWEEN THE BOTTLES AND REPORTED THE LOT # FP7137 WAS USED FOR VACCINATION WHICH IS PRIMARY MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 98,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
FACILITY BELIEVES THEY GAVE PRIMARY MONOVALENT VACCINE IN ERROR FOR BIVALENT VACCINE. NURSING COULD NOT TELL THE DIFFERENCE BETWEEN THE BOTTLES AND REPORTED THE LOT # FP7137 WAS USED FOR VACCINATION WHICH IS PRIMARY MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
FACILITY BELIEVES THEY GAVE PRIMARY MONOVALENT VACCINE IN ERROR FOR BIVALENT VACCINE. NURSING COULD NOT TELL THE DIFFERENCE BETWEEN THE BOTTLES AND REPORTED THE LOT # FP7137 WAS USED FOR VACCINATION WHICH IS PRIMARY MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
FACILITY BELIEVES THEY GAVE PRIMARY MONOVALENT VACCINE IN ERROR FOR BIVALENT VACCINE. NURSING COULD NOT TELL THE DIFFERENCE BETWEEN THE BOTTLES AND REPORTED THE LOT # FP7137 WAS USED FOR VACCINATION WHICH IS PRIMARY MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
FACILITY BELIEVES THEY GAVE PRIMARY MONOVALENT VACCINE IN ERROR FOR BIVALENT VACCINE. NURSING COULD NOT TELL THE DIFFERENCE BETWEEN THE BOTTLES AND REPORTED THE LOT # FP7137 WAS USED FOR VACCINATION WHICH IS PRIMARY MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
FACILITY BELIEVES THEY GAVE PRIMARY MONOVALENT VACCINE IN ERROR FOR BIVALENT VACCINE. NURSING COULD NOT TELL THE DIFFERENCE BETWEEN THE BOTTLES AND REPORTED THE LOT # FP7137 WAS USED FOR VACCINATION WHICH IS PRIMARY MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 27.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
FACILITY BELIEVES THEY GAVE PRIMARY MONOVALENT VACCINE IN ERROR FOR BIVALENT VACCINE. NURSING COULD NOT TELL THE DIFFERENCE BETWEEN THE BOTTLES AND REPORTED THE LOT # FP7137 WAS USED FOR VACCINATION WHICH IS PRIMARY MONOVALENT VACCINE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 01.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
VACCINE WAS POSSIBLY PAST THE BUD AT VACCINATION ACCORDING TO THE VACCINE RECORD. NURSE REPORTED ON VACCINE RECORD THAT VACCINE WAS GIVEN ON 11/1/22 BUT VIAL WAS OPENED ON 10/27/22. UNABLE TO CONFIRM IF INDIVIDUAL WAS VACCINATED ON 10/27 OR 11/1.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 01.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
VACCINE WAS POSSIBLY PAST THE BUD AT VACCINATION ACCORDING TO THE VACCINE RECORD. NURSE REPORTED ON VACCINE RECORD THAT VACCINE WAS GIVEN ON 11/1/22 BUT VIAL WAS OPENED ON 10/27/22. UNABLE TO CONFIRM IF INDIVIDUAL WAS VACCINATED ON 10/27 OR 11/1.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 31.10.2022
- Beginn
- 31.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
VACCINE WAS POSSIBLY PAST THE BUD AT VACCINATION ACCORDING TO THE VACCINE RECORD. NURSE REPORTED ON VACCINE RECORD THAT VACCINE WAS GIVEN ON 10/31/22 BUT VIAL WAS OPENED ON 10/27/22. UNABLE TO CONFIRM IF INDIVIDUAL WAS VACCINATED ON 10/27 OR 10/31.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 22.02.2023
- Impfdatum
- 01.10.2021
- Beginn
- 10.01.2022
- Tage bis Beginn
- 101,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Nasal congestion
SARS-CoV-2 test positive
Symptomtext
On 10/01/2021 I received my Covid-19 vaccine. On 01/10/2022 I woke up with a stuffy nose and cough. After reaching out to my doctor I was prescribed steroids for a week and symptoms went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetic
- Andere Medikamente
- Metformin; TRESIBA; LIPITOR; PLAVIX; aspirin; metoprolol; NEURONTIN; fluticasone; calcium; vitamin D3; vitamin B12; cranberry; coQ10; METAMUCIL; TYLENOL; turmeric
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 07.02.2023
- Impfdatum
- 04.08.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 21,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cardiac monitoring abnormal
Heart rate increased
SARS-CoV-2 test positive
Symptomtext
I had got COVID-19. It started off with a heart attack like symptoms. I had a rapped heartbeat. I wore a heart monitor. It kept saying it was abnormal. I was referred to a cardiologist that put me on medication. I then was referred to a heart surgeon. I am now going to have a procedure done called Catheter Ablation. I am unsure if it is COVID or vaccination related. I have now recovered from COVID-19. I did have to go the emergency room and get a higher dose of my heart medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 25AUG2022 COVID-19 positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Heart Condition
- Andere Medikamente
- Multivitamin; estrogen patch
- Allergien
- Wheat products; penicillin
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 07.02.2023
- Impfdatum
- 04.08.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 91,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests abnormal
Balance disorder
COVID-19
Deafness unilateral
SARS-CoV-2 test positive
Tinnitus
Symptomtext
I had vaccine in August, first week of November I got COVID, after having a COVID-19 home test on Nov 3rd, I was positive. At the end of Nov, I had a loud sound in my ear, my balance was bad, and went to the doctor on Nov 30th, and mentioned this to the doctor and he referred me to have a hearing test and when I got the results it was a dramatic decrease on my left ear, the inner ear. I always had problem in my ear, but this time was disruptive. I will have an MRI of the brain on Feb 15th and, on the 28th of February I will have follow up with my doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests abnormal
- Hospital-Tage
- -
- Labordaten
- 03NOV2022 COVID-19 test positive; 17Jan2023 Audiogram Hearing Test abnormal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Diabetes II; High Blood Pressure, High Cholesterol; Arthritis; Hemophilia
- Andere Medikamente
- N/A
- Allergien
- CIPRO; sulfa; hydrochlorothiazide
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 23.01.2023
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
ADMINISTRATION ERROR: 2ND DOSE OF PRIMARY SERIES WITH PFIZER COVID-19 MONOVALENT VACCINE WAS GIVEN TOO SOON. IT WAS ONLY 13 DAYS AFTER 1ST DOSE. 1ST DOSE ON 10/26/22 AND 2ND DOSE ON 11/8/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 18.01.2023
- Impfdatum
- 09.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
PT RECIEVED PFIZER GREY TOP FOR 12+ AS A BOOSTER DOSE INSTEAD OF ORANGE TOP AGES 5-11 NO TREATMENT GIVEN AND NO HARM TO PATIENT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE KNOWN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- 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: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 10.01.2023
- Impfdatum
- 19.10.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 10.01.2023
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 09.01.2023
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Error: Improper Storage (ex. temp./location)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 20.12.2022
- Beginn
- 20.12.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Employee reported to hospital for second dose of COVID vaccine (Pfizer) on 12/20/22; dose was administered. Upon entering into system on 12/21/22, it is noted that the first dose was administered on 12/12/22. Therefore, the second dose was administered 7 days after the first dose. Employee was notified on 12/21/22, she reports that she is feeling fine and is not having any side effects. Employee did not have any adverse effects to date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- Not applicable
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- No.
- Andere Medikamente
- No.
- Allergien
- Toradol
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 14.12.2022
- Impfdatum
- 20.08.2022
- Beginn
- 05.12.2022
- Tage bis Beginn
- 107,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Investigation
Nasopharyngeal swab
SARS-CoV-2 test
Scan brain
Symptomtext
Covid positive after vaccines and boosters; Covid positive after vaccines and boosters; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. An 80-year-old female patient received BNT162b2 (BNT162B2), on 22Jan2021 as dose 1, single (Lot number: EL9262), on 02Feb2021 as dose 2, single (Lot number: EL9269), on 18Oct2021 as dose 3 (booster) , single (Lot number: FE3590) and on 20Aug2022 as dose 4 (booster), single (Lot number: FP7137) at the age of 79 years for covid-19 immunisation. The patient's relevant medical history included: "COVID-19" (unspecified if ongoing), notes: COVID-19 Caller has had Covid 19 a total of three times. States that she cannot remember the dates or time frames for the first two times she had Covid 19. Concomitant medication(s) included: ARICEPT. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 05Dec2022, outcome "not recovered" and all described as "Covid positive after vaccines and boosters". The patient underwent the following laboratory tests and procedures: Flu test: (unspecified date) Negative, notes: Doctor also tested her for the flu and another test that they swab for, but both of those were negative; Nasopharyngeal swab: (unspecified date) Negative, notes: Doctor also tested her for the flu and another test that they swab for, but both of those were negative; SARS-CoV-2 test: (05Dec2022) Positive; Scan brain: (05Dec2022) Unknown results, notes: The doctor did a brain scan. Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical course: COVID-19 Caller has had Covid 19 a total of three times. States that she cannot remember the dates or time frames for the first two times she had Covid 19. Her most recent positive Covid 19 test, for her third time having it, was on 05Dec2022. Patient was received Paxlovid as treatment (Start: 05Dec2022 Stop: Ongoing). Paxlovid, the medication they gave her for Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: Flu test; Test Result: Negative ; Comments: Doctor also tested her for the flu and another test that they swab for, but both of those were negative; Test Name: Swab; Test Result: Negative ; Comments: Doctor also tested her for the flu and another test that they swab for, but both of those were negative; Test Date: 20221205; Test Name: COVID test; Test Result: Positive ; Test Date: 20221205; Test Name: Brain Scan; Result Unstructured Data: Test Result:Unknown results; Comments: The doctor did a brain scan
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (COVID-19 Caller has had Covid 19 a total of three times.)
- Andere Medikamente
- ARICEPT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Incorrect product formulation administered
Wrong product administered
Symptomtext
Vaccine was administered in error, as it was not the bivalent vaccine and had expired on 10/05/2022. No reported adverse outcomes resulting from event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 13.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Incorrect product formulation administered
Wrong product administered
Symptomtext
Vaccine was administered in error, as it was not the bivalent vaccine and had expired on 10/05/2022. No reported adverse outcomes as a result of the event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Incorrect product formulation administered
No adverse event
Product administration error
Wrong product administered
Symptomtext
Vaccine was administered in error, as it was not the bivalent vaccine and had expired on 10/5/2022. No reported adverse outcomes as a result of the event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Incorrect product formulation administered
No adverse event
Product administration error
Wrong product administered
Symptomtext
Vaccine was administered in error, as it was not the bivalent vaccine and had expired on 10/5/2022. No reported adverse outcomes as a result of the event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Incorrect product formulation administered
Wrong product administered
Symptomtext
Vaccine was administered in error, as it was not the bivalent vaccine and had expired on 10/5/2022. No reported adverse outcomes as a result of the event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Incorrect product formulation administered
Wrong product administered
Symptomtext
Vaccine administered in error, as it was not the bivalent vaccine and had expired on 10/5/2022. No reported adverse outcomes as a result of the event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 13.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Incorrect product formulation administered
Wrong product administered
Symptomtext
Vaccine was administered in error, as it was not the bivalent vaccine and had expired on 10/5/2022. No reported adverse outcomes as a result of the event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Wrong product administered
Symptomtext
Vaccine was administered in error, as it was not bivalent and had expired on 10/5/2022. No adverse outcomes resulted from the event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 13.12.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Wrong product administered
Symptomtext
Vaccine was administered in error, as it was not bivalent and had expired on 10/5/2022. No adverse outcomes resulted from the event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 26.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
GIVEN 33 DAYS BUD OF 9/23/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 11.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Given 33 days BUD from 9/23/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 17.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Given 24 days BUD of 9/23/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 22.11.2022
- Impfdatum
- 27.09.2022
- Beginn
- 27.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient recieved the Pfizer Lot FP7137 ( which is a monovalent COVID-19 vaccine) for his booster instead of the Bivalent booster. He was made aware of this and can receive the booster bivalent shot after two months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 22.11.2022
- Impfdatum
- 21.11.2022
- Beginn
- 21.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Covid19 Pfizer 12 and up was given and was expired on 11-7-22. No reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
upon discovery from the administrator of the shot, and errant dose of Pfizer-BioNTech COVID-19 vaccine with a LOT of FP7137 instead of the Bivalent Pfizer Booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- no applicable
- Aktuelle Erkrankungen
- no illnesses at present
- Vorgeschichte
- no medical history
- Andere Medikamente
- no history
- Allergien
- no history
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 18.11.2022
- Impfdatum
- 18.11.2022
- Beginn
- 18.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
upon discovery from the administrator of the shot, and errant dose of Pfizer-BioNTech COVID-19 vaccine with a LOT of FP7137 instead of the Bivalent Pfizer Booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- not applicable
- Aktuelle Erkrankungen
- no illnesses at present
- Vorgeschichte
- no history
- Andere Medikamente
- no history
- Allergien
- penicillin according to patient
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Patient was given a Covid booster with the Pfizer monovalent vaccine instead of the Pfizer bivalent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 15.11.2022
- Impfdatum
- 15.11.2022
- Beginn
- 15.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Patient was given a Covid booster with the Pfizer monovalent vaccine instead of the Pfizer bivalent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 15.11.2022
- Impfdatum
- 06.09.2022
- Beginn
- 06.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Late in the day on 8/31/22, the FDA rescinded the EUA order for the use of the monovalent Pfizer and Moderna vaccine as boosters for people aged 12 years and older. The information took a little time to trickle from the Government to local staff and then to our clinic and the staff administering vaccine. Because of this delay, some monovalent vaccine throughout the HCF was inadvertently given after 8/31/22. The CDC stated that any monovalent vaccine administered as a booster dose after the EUA was rescinded would be considered a vaccine error. At a recent Immunization Subcommittee meeting, we discussed this and our medical providers stated that any monovalent vaccine given as a booster dose on 9/1/2022 or after should have VAERS report completed on them per the CDC's requirements.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 10.11.2022
- Impfdatum
- 28.10.2022
- Beginn
- 28.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Patient was given the wrong vaccine for his COVID Booster. He was given the Monovalent instead of the Bivalent dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No Known illness at the time of vaccination
- Vorgeschichte
- Hypothyroidism, Diabetes Mellitus, Hypertension and Fatty Liver
- Andere Medikamente
- Amlodipine 10 mg, Atorvastatin 10 mg, Levothyroxine 88 mcg and Metoprolol Tartrate 25 mg
- Allergien
- Metformin - causes severe lactic acidosis
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 09.11.2022
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Pfizer Monovalent vaccine was given instead of Bivalent vaccine which was requested
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Pfizer Monovalent vaccine was given instead of Bivalent vaccine which was requested
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 09.11.2022
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Pfizer Monovalent vaccine was given instead of Bivalent vaccine which was requested
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 94,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Pfizer Monovalent vaccine given instead of Bivalent which was requested
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 08.11.2022
- Beginn
- 08.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Pfizer Monovalent vaccine given instead of Bivalent which was requested
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 09.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
At 1353, client received two vaccines: Fluarix Quadrivalent lot # 9PG4D, and Pfizer first dose, lot # FP7137. At approximately 1406 client reported "whistling in ears". PHN asked client if it felt like a "ringing" sound or sensation, and client replied, "yes". Client stated that he had no other symptoms, had never experienced a "ringing" or "whistling" in his ears, and that the sensation began when he stood up after being vaccinated. PHN advised client to stay under observation for another 15 minutes and to follow up with PCP. Client stated does not have PCP and stated desire to "step outside? and remove his mask. PHN stated would give client a list of community clinics. Client left the premises on foot and did not return.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 09.08.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 86,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Ear discomfort
Feeling hot
Insomnia
Paranasal sinus discomfort
Respiratory tract congestion
SARS-CoV-2 test positive
Throat irritation
Symptomtext
Starting 11/02/2022, I had a bit of a scratchy throat. The next day I had more of a scratchy throat and congestion/sinus pressure. I tested myself for COVID-19 at home and it was positive. The next day, on Friday, I had a lot of sinus pressure and periods of feeling hot without a fever. I had a hard time cooling off. I called my doctor and they prescribed Paxlovid (which I started later that afternoon). No coughing to a large degree. The scratchy throat disappeared. Friday the symptoms were mainly sinus pressure, insomnia and temperature regulation. Today, I am still a little congested and my right ear is still clogged. I basically feel like I am recovering from a cold but doing better than expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- At-home COVID-19 test (11/03/2022): Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; Pre-diabetes
- Andere Medikamente
- Benicar HCT; Zyrtec; Advil Dual Action
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 08.11.2022
- Impfdatum
- 04.11.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Patient was given original COVID vaccine instead of the BIVALENT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 04.11.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient was given the original COVID vaccine instead of the Bivalent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 10.09.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Wrong product administered
Symptomtext
I was supposed to receive the Moderna Bivalent booster, but was given the Pfizer original formulation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 07.11.2022
- Impfdatum
- 04.11.2022
- Beginn
- 04.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Patient was given incorrect COVID vaccine, should have received the Bivalent vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 05.11.2022
- Impfdatum
- 05.11.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- -
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Patient Did not present to nurse with proof of vaccination. Self-attested to native language speaking nurse and certified translator that she had only had one dose of COVID-19 vaccine. Because primary dose was to be documented on a form, when we logged into the state vaccine registry, we discovered that she had had 3 monovalent Pfizer shots with the last one being recorded on 09/28/2022. She was not yet eligible to receive the bivalent booster, and received a 4th monovalent dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 04.11.2022
- Impfdatum
- 18.10.2022
- Beginn
- 18.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Pfizer COVID vaccine administered one week early.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 03.11.2022
- Impfdatum
- 03.11.2022
- Beginn
- 03.11.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
No adverse event
Symptomtext
old Pfizer was drawn instead of the new bivalent Pfizer vaccine. no adverse reactions reported but meant to give pt the new bivalent vaccine. spoke with pt and recommended to come back after 2 months to receive the bivalent pzifer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 02.11.2022
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Wrong product administered
Symptomtext
No adverse event or treatment needed. On 09/27/2022 our organization did not yet have the bivalent booster, so this patient was given the monovalent dose. They have been contacted and instructed to get the bivalent booster 2 months after their last dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 31.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 9,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
VACCINE GIVEN 14 DAYS (10/18/22) AFTER USE BY DATE(10/4/22)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- PEANUT
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 31.10.2022
- Impfdatum
- 26.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
VACCINE WAS GIVEN 22 DAYS(10/26/22) AFTER USE BY DATE(10/4/22)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- AUTISM
- Andere Medikamente
- METHYLPHENIDATE HCI ER 20 MG
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 31.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 13,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
VACCINE GIVEN 10 DAYS (10/14/22) AFTER USE BY DATE (10/4/22)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- DROSPIRENONE-ETHINYL ESTRADIOL 3-0.03
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 31.10.2022
- Impfdatum
- 10.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 17,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
VACCINE GIVEN 6 DAYS AFTER USE BY DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 25.10.2022
- Beginn
- 25.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
No adverse reaction. Gave monovalent instead of bivalent. Patient will return in 2 months for the bivalent dose.
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
- TN
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 28.10.2022
- Impfdatum
- 26.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
MONOVALENT VACCINE WAS GIVEN INSTEAD OF BIVALENT BOOSTER THAT WAS NEEDED. NURSE DISCOVERED THIS ERROR THE NEXT DAY AFTER VACCINATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE REPORTED
- Vorgeschichte
- NOT KNOWN
- Andere Medikamente
- NOT KNOWN
- Allergien
- NONE LISTED
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 28.10.2022
- Impfdatum
- 26.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
MONOVALENT VACCINE WAS GIVEN INSTEAD OF BIVALENT BOOSTER THAT WAS NEEDED. NURSE DISCOVERED THIS ERROR THE NEXT DAY AFTER VACCINATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE LISTED
- Vorgeschichte
- NOT KNOWN
- Andere Medikamente
- NOT KNOWN
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 28.10.2022
- Impfdatum
- 26.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
MONOVALEN VACCINE WAS GIVEN INSTEAD OF BIVALENT BOOSTER THAT WAS NEEDED. NURSE DISCOVERED THIS ERROR THE NEXT DAY AFTER VACCINATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE REPORTED
- Vorgeschichte
- NOT KNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE LISTED
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 28.10.2022
- Impfdatum
- 26.10.2022
- Beginn
- 27.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
MONOVALENT DOSE GIVEN INSTEAD OF BIVALENT BOOSTER DOSE THAT WAS NEEDED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE KNOWN
- Vorgeschichte
- HYPERTENSION, DIABETES, HYPERLIPIDEMIA, DIVERTICULOSIS, GOUT
- Andere Medikamente
- VICTOZA, LEVEMIR, NEXIUM, TRILIPIX, ALLOPURINOL, METFORMIN, METOPROLOL, LISINOPRIL, ATORVASTATIN, AMLODIPINE, VIT D, VIT B12, MAGNESIUM, ALBUTEROL INHALER
- Allergien
- NONE KNOWN
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 27.10.2022
- Impfdatum
- 26.10.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given Monovalent Covid vaccine that was BUD on 10/24/22. The manufacturer expiration date was 11/30/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 91,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
patient came in office to obtain the COVID19 (Pfizer-BioNTech Bivalent dose. patient was given the Monovalent dose by error. Patient was let known of what was given and patient stated she had no symptoms but would still like to obtain the Bivalent dose after time frame period. This is patient 4 dose of the Monovalent and per Dr. Patient is able to continue with no further directions .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
None -- Pfizer 12 and up Monovalent given instead of Bivalent as incorrect booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HTN GERD Metabolic Syndrome Obesity Migraine OSA
- Andere Medikamente
- Escitalopram 20mg Pantoprazole 40mg Diclofenac 1% topical gel Betamethasone 0.05% topical lotion norethindrone 5mg gabapentin 100mg metoprolol ER 200mg tablet rizatriptan 5mg ODT Losartan 50mg Hyoscycamine 0.375mg exended release tablet Met
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 25.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
No Adverse Event reported by patient -- Pfier 12 and up monovalent given instead of Bivalent (incorrect booster)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes Mellitus, Type 2 Diabetic Neuropathy Hyperlipidemia Hypovitaminosis D Migraine Disorder Obesity
- Andere Medikamente
- Atorvastatin 20mg Nortriptyline 10mg Pregabalin 75mg Emtricitabine / Tenofivir 200/300mg Ertugliflozin 15mg Sildenafil 50mg Semaglutide 1mg Metformin ER 500mg Glimepiride 4mg Cholecalciferol 2000 IU
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 25.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
No adverse event -- 12 and up Pfizer Monovalent was given instead of Bivalent COVID-19 Vaccine as booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin C 500mg
- Allergien
- No Known Allergies
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient was to receive the Bivalent COVID 12 years and up vaccine and instead received the Monovalent COVID 12 years and up in error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient was to receive the Bivalent COVID 12 years and up instead received Monovalent COVID 12 years and up in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 25.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
patient was to receive the Bivalent COVID 12 years and up instead they received the Monovalent COVID 12 years and up in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient was to receive the Bivalent COVID 12 years and up. Patient received the Monovalent COVID 12 years and up in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 25.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient was to receive Bivalent COVID 12 years and up at visit. Patient actually received Monovalent COVID 12 years and up
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Elavil, Norvasc, Neurontin, Cozaar, Macrobid, Phenergan, Zanaflex
- Allergien
- Nickel, Adhesive
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 25.10.2022
- Impfdatum
- 24.10.2022
- Beginn
- 24.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient was supposed to receive the Bivalent vaccine and instead received the Monovalent years and up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ADHD Depression
- Andere Medikamente
- Wellbutrin, Concerta, Zoloft
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 23.10.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient incorrectly received the orig. Pfizer vaccine INSTEAD of the intended vaccine---Pfizer Bi-valent!!!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 23.10.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient incorrectly received the orig. Pfzier vaccine and NOT the intended vaccine--Pfizer Bi-valent!!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 23.10.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient wrongly received the orig. Pfizer vaccine INSTEAD of the Pfizer Bi-valent Vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 23.10.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient incorrectly received the orig. Pfizer vaccine. Patient's intended vaccine---Pfizer Bi-valent!!! Again, incorrectly received the orig. Pfzier and NOT the intended vaccine--Pfizer Bivalent!!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 23.10.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient received the orig. Pfizer Vaccine instead of the Pfizer Bivalent Dose!!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 23.10.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
On 10/21 the plain Pfizer Vaccine was administered to this patient. She was supposed to receive the PFIZER-BIVALENT DOSE (NOT the orig.vacc)!!!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Macrolides
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 23.10.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient was administered the plain Pfizer vaccine---INSTEAD of the Pfizer bi-valent vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 23.10.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient was administered the orig. Pfizer vaccine INSTEAD of the Pfizer-Bivalent vaccine!!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 23.10.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient received the plain pfizer vaccine instead of the Pfizer bivalent dose. Intended shot--Pfizer Bivalent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 23.10.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient wrongly was administered the plain Pfizer Vaccine and NOT the bi-valent Pfizer vaccine. Bivalent dose was intended dose (NOT given).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 23.10.2022
- Impfdatum
- 21.10.2022
- Beginn
- 21.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
The vaccine given was the orig. Pfizer vaccine. It was supposed to be the bi-valent version of Pfizer!!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 22.10.2022
- Impfdatum
- 22.10.2022
- Beginn
- 22.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product use issue
Symptomtext
Patient was given a shot that was 15 days past BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product use issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 22.10.2022
- Impfdatum
- 25.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
COVID-19; COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP) from medical information team. The reporter is the patient. An 83-year-old female patient received BNT162b2 (BNT162B2), on 27Jan2021 as dose 1, single (Lot number: EL3246), in left arm, on 17Feb2021 as dose 2, single (Lot number: EN6198), in left arm, on 24Sep2021 as dose 3 (booster), single (Lot number: 301458A), in left arm and on 25Jul2022 as dose 4 (booster), single (Lot number: FP7137) at the age of 82 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "Kidney disease" (unspecified if ongoing), notes: Mild to moderate Kidney disease.Diagnosed about 3 years ago, caused by high blood pressure.; "high blood pressure" (unspecified if ongoing), notes: Mild to moderate Kidney disease. Diagnosed about 3 years ago, caused by high blood pressure. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive; Positive, notes: She tested positive for Covid twice. Therapeutic measures were taken as a result of vaccination failure, covid-19. Clinical course information: She does not know if she should stop taking the medication or not. She's gotten the Covid vaccines and has been vaccinated and boosted twice and has taken two days worth of medication. She plans on taking it at least one more day because she knows it has good results.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Positive ; Test Name: COVID-19 test; Test Result: Positive ; Comments: She tested positive for Covid twice
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Blood pressure high (Mild to moderate Kidney disease. Diagnosed about 3 years ago, caused by high blood pressure.); Kidney disorder (Mild to moderate Kidney disease.Diagnosed about 3 years ago, caused by high blood pressure.)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 06.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
patient received the Pfizer monovalent booster instead of the Pfizer bivalent booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Unknown
- Andere Medikamente
- No
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 21.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient administered Pfizer 12 &up MRNA verses Pfizer 12&UP Bivalent, no reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- generalized anxiety disorder
- Andere Medikamente
- Allegra 12 hour, singulair 10mg one daily, escitalopram 10mg one daily, estarylla 0.25mg one daily
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 21.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
Patient administered Pfizer 12 & up MRNA vaccine verses Pfizer 12 & Up Bivalent vaccine. No reaction. Incorrect Booster administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- hypothyroid, hodgkins disease
- Andere Medikamente
- Levothyroxine 150mcg one daily, multivitamin daily, zyrtec 10mg daily
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 20.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
patient was administer pfizer monovalent instead of bivalent for booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
patient was administered pfizer monovalent instead of bivalent for booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
patient was administered pfizer monovalent instead of bivalent for booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 20.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 20.10.2022
- Tage bis Beginn
- 2,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient was administered monovalent instead of bivalent for booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 20.10.2022
- Impfdatum
- 18.10.2022
- Beginn
- 18.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Patient was administered expired vaccine- No adverse events
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- Diabetes type 2 Anxiety Austism Spectrum Disorder Speech Delay Sleep Disturbances
- Andere Medikamente
- Invuniv, Levemir, Glucophage, Risperdal, Zoloft
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 19.10.2022
- Impfdatum
- 19.10.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient was administered pfizer monovalent instead of bivalent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 19.10.2022
- Impfdatum
- 19.10.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
patient was administered pfizer monovalent not bivalent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 19.10.2022
- Impfdatum
- 19.10.2022
- Beginn
- 19.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 6
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Patient received monovalent vaccine instead of bivalent vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 19.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 19.10.2022
- Impfdatum
- 11.08.2022
- Beginn
- 18.10.2022
- Tage bis Beginn
- 68,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID BREAKTHROUGH CASE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 10/18/22 COVID+
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, Bipolar, schizophrenia
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 13.10.2022
- Beginn
- 13.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
On 10/13/2022 an employee administered the pfizer monovalent 0.2ml vaccine instead of the pfizer 5-11 yr bivalent vaccine. The Dr. on site called and spoke to the parent. Staff in the office has been spoken to and more verification in specific is to be done before a vaccine is administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 18.10.2022
- Impfdatum
- 17.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Pt. received monovalent, but wanted bivalent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 17.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Pt. received monovalent, but wanted bivalent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 17.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Pt. received monovalent, but wanted bivalent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 18.10.2022
- Impfdatum
- 17.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Pt. received monovalent vaccine when wanted bivalent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 18.10.2022
- Impfdatum
- 03.10.2022
- Beginn
- 03.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
The vaccine was stored at room temperature longer than the recommended time. Patient did NOT experience any adverse events but will require another vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 18.10.2022
- Impfdatum
- 17.10.2022
- Beginn
- 17.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
The patient had received a Janssen in January 2022 as his first COVID vaccine dose. He presented today for a booster and was administered a monovalent Pfizer (gray cap) instead of the bivalent Pizer. I am reporting a vaccine error- none an adverse event at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- not known
- Vorgeschichte
- not known
- Andere Medikamente
- not known
- Allergien
- not known
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 14.10.2022
- Impfdatum
- 14.10.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Pt was given Pfizer Monovalent instead of Moderna Bivalent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None that we were aware of.
- Vorgeschichte
- Major Depressive Disorder, Obesity, Impaired Mobility and ADL's, Hypertension, Prediabetic, Bilat Chronic Knee Pain
- Andere Medikamente
- Amlodipine, Atorvastatin, Escitalopram, Losartan, Aleve
- Allergien
- Aleve
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- -
- Geschlecht
- U
- Eingang
- 14.10.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Product administration error
Symptomtext
The clinic did not see email to stop giving the original (monovalent) COVID until after the Moderna -monovalent was given on 9/2/22. The other 4 were administration errors, patients were given a dose of COVID monovalent instead of Bivalent by MA mistake. DOS 9/7/22, 9/9/22, 9/23/22, 9/30/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- -
- Geschlecht
- U
- Eingang
- 14.10.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Product administration error
Symptomtext
The clinic did not see email to stop giving the original (monovalent) COVID until after the Moderna -monovalent was given on 9/2/22. The other 4 were administration errors, patients were given a dose of COVID monovalent instead of Bivalent by MA mistake. DOS 9/7/22, 9/9/22, 9/23/22, 9/30/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- -
- Geschlecht
- U
- Eingang
- 14.10.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Clinic did not see the email to stop giving original(monovalent) Pfizer 12+ until after these 3 shots were given -1 given 9/1/22 and 2 given 9/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- -
- Geschlecht
- U
- Eingang
- 14.10.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Clinic did not see the email to stop giving original(monovalent) Pfizer 12+ until after these 3 shots were given -1 given 9/1/22 and 2 given 9/2/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 30.09.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 12,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
TC to patient to explained that expired vaccine was administer on 9/30.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- No
- Andere Medikamente
- N/A
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 08.10.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient indicated for bivalent booster. Received monovalent booster instead.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknwn
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 27.07.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Thyroid hormones test
Symptomtext
COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non-HCP). The reporter is the patient. A 76-year-old female patient received BNT162b2 (BNT162B2), on 27Jul2022 as dose 4 (booster), single (Lot number: FP7137) at the age of 75 years, in right arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown), as dose 2, single (Batch/Lot number: unknown) and as dose 3 (booster), single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "pernicious anemia" (unspecified if ongoing); "low thyroid" (unspecified if ongoing), notes: low thyroid; "known allergies: sulfa" (unspecified if ongoing), notes: known allergies: sulfa; "known allergies: fusarium mold" (unspecified if ongoing), notes: known allergies: fusarium mold. The patient's concomitant medications were not reported. Past drug history included: Known allergies: cipro, reaction(s): "Allergy", notes: known allergies: cipro. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (unspecified date) positive, notes: I took five full days of Paxlovid after testing positive for COVID; (08Oct2022) negative, notes: A COVID test on 08Oct was negative; Thyroid hormones test: (unspecified date) low, notes: low thyroid. Therapeutic measures were taken as a result of drug ineffective, covid-19. The patient received treatment with Paxlovid from 28Sep2022 to 02Oct2022 for covid-19. It was reported that patient took five full days of Paxlovid after testing positive for COVID. Last does was 02Oct. On 08Oct symptoms returned: congestion, feeling tired and achey. A COVID test on 08Oct was negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID; Test Result: Positive ; Comments: I took five full days of Paxlovid after testing positive for COVID.; Test Date: 20221008; Test Name: COVID; Test Result: Negative ; Comments: A COVID test on 08Oct was negative.; Test Name: thyroid; Result Unstructured Data: Test Result:low; Comments: low thyroid
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy to molds (known allergies: fusarium mold); Hypothyroidism (low thyroid); Pernicious anemia; Sulfonamide allergy (known allergies: sulfa)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 13.10.2022
- Impfdatum
- 24.07.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 39,0
- Dosis
- 4
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP) from product quality group. The reporter is the patient. A 63-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 08Oct2021 as dose 3 (booster), single (Lot number: 301458A), in left arm and on 24Jul2022 as dose 4 (booster), single (Lot number: FP7137) at the age of 63 years, in left arm for covid-19 immunisation; coviD-19 vaccine (COVID-19 VACCINE), as dose 1, single (Batch/Lot number: unknown) and as dose 2, single (Batch/Lot number: unknown) for covid-19 immunisation. The patient's relevant medical history included: "Hypothyroidism" (unspecified if ongoing). Concomitant medication(s) included: LEVOTHYROXIN, start date: Jan2010; CALCIUM, start date: Jan2000; GLUCOSAMINE CHONDROITIN [CHONDROITIN SULFATE;GLUCOSAMINE], start date: Oct2021; COLLAGEN, start date: Nov2017; VITAMIN D [COLECALCIFEROL], start date: Aug2021. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset Sep2022, outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Additional information: Patient's concomitant medication also included VitreousHealth. Follow-up attempts are completed. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hypothyroidism
- Andere Medikamente
- LEVOTHYROXIN; CALCIUM; GLUCOSAMINE CHONDROITIN [CHONDROITIN SULFATE;GLUCOSAMINE]; COLLAGEN; VITAMIN D [COLECALCIFEROL]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 12.10.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
Pfizer Monovalent given to 10 patients instead of Pfizer Bi-Valent Booster. All 10 patients had no Adverse reaction to Mono-valent vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 12.10.2022
- Impfdatum
- 09.10.2022
- Beginn
- 09.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 12.10.2022
- Impfdatum
- 11.10.2022
- Beginn
- 11.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
The patient was given the second dose of the Pfizer vaccine; the vaccine's beyond use date was 10/5/22, and the vaccine was given 10/11/22. The vaccine's expiration date was 11/30/22. As of now, the patient has not reported any adverse effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 11.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
No adverse event
Symptomtext
Pt was given COVID19 Pfizer-BioNTech instead of COVID19 Pfizer-BioNTech Bivalent. Vials look very similar in size, color. The wrong vial was pulled in order to draw up and administer. Pt tolerated injection well and was monitored for 15 minutes post injection. No adverse effects noted. Pt tolerated well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 11.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Unevaluable event
Symptomtext
PT was to receive the Pfizer bivalent booster, abut was mistakenly administered the monvalent Pfizer instead
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- no
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 11.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Unevaluable event
Symptomtext
PT was to receive the Pfizer bivalent booster, abut was mistakenly administered the monvalent Pfizer instead
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- no
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 11.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Unevaluable event
Symptomtext
PT should have received a Bi-Valent booster dose, but instead was mistakenly administered a mono-valent Pfizer dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 11.10.2022
- Impfdatum
- 01.10.2022
- Beginn
- 01.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Unevaluable event
Symptomtext
PT should have received a Bi-Valent booster dose, but instead was mistakenly administered a mono-valent Pfizer dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 10.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient received original Pfizer vaccine when came in for the new bivalent Pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient received original Pfizer vaccine when came in for the new bivalent Pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient received original Pfizer vaccine when came in for the new bivalent Pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 10.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient received original Pfizer vaccine when came in for the new bivalent Pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient received original Pfizer vaccine when came in for the new bivalent Pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 07.10.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient received original Pfizer vaccine when came in for the bivalent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
patient was given monovalent instead of bivalent vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- not applicable
- Aktuelle Erkrankungen
- no acute illnesses
- Vorgeschichte
- hypertension, dyslipidemia, impaired glucose tolerance, allergic rhinitis, tubular adenopma of colon, GERD, ED, BPH, spondylosis of lumbar region
- Andere Medikamente
- azelastine, chlorthalidone, fexofenadine, multivitamin pravastatin, sildenafil
- Allergien
- kenalog, penicillin, rosuvastatin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
patient given monovalent vaccine instead of bivalent vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- not applicable
- Aktuelle Erkrankungen
- no acute illnesses
- Vorgeschichte
- dyslipidemia, impaired glucose tolerance, hearing loss, osteopenia bilateral hips, insomnia
- Andere Medikamente
- multivitamin
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 10.10.2022
- Impfdatum
- 10.10.2022
- Beginn
- 10.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
patient was given monovalent vaccine instead of bivalent vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- not applicable
- Aktuelle Erkrankungen
- no acute illnesses
- Vorgeschichte
- OSA, parkinsonism due to drug, postural kyphosis, schizophrenia, OCD, BPH, hyponatremia, GERD, oropharyngeal dysphagia, hypothyroidism, impaired fasting glucose, thrombocytopenic disorder, peripheral venous insufficiency, mixed hypercholesterolemia and hypertriglyceridemia
- Andere Medikamente
- benztropine, buspirone, calcium, citalopram, chlorhexidine, divalproex, finasteride, gabapentin, levothyroxine, multivitamin, pantopraxole, risperidone, triazolam, vitamin e
- Allergien
- bee venom
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 06.10.2022
- Beginn
- 06.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Error: Expired Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 08.10.2022
- Impfdatum
- 26.07.2022
- Beginn
- 07.10.2022
- Tage bis Beginn
- 73,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asymptomatic COVID-19
Exposure to SARS-CoV-2
SARS-CoV-2 test positive
Symptomtext
tested as follow up to known exposure from roommate, asymptomatic, tested positive on Abbott ID Now molecular test has had 3 doses of pfizer, due for bivalent booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hx CVA, htn, ckd3, ashd
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 07.10.2022
- Impfdatum
- 21.09.2022
- Beginn
- 21.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Administration Error, Incorrect mRNA COVID-19 vaccine product was administered as a 3rd dose booster instead of Bivalent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Product administration error
Symptomtext
Administration Error, Incorrect mRNA COVID-19 vaccine product was administered as a 3rd dose booster instead of Bivalent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
No adverse event
Symptomtext
Patient was to receive the new bivalent vaccine booster. Due to the original Pfizer vaccine being in a grey top as well it was accidently mistaken for the new bivalent which is also a grey top. 0.3 ml was given. patient does not have any adverse reactions at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 07.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
Patient was to receive the new bivalent vaccine booster. Due to the original Pfizer vaccine being in a grey top as well it was accidently mistaken for the new bivalent which is also a grey top. 0.3 ml was given. patient does not have any adverse reactions at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 06.10.2022
- Impfdatum
- 30.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
SARS-CoV-2 test
Symptomtext
COVID-19 Treatment; COVID-19 Treatment; This is a spontaneous report received from a non-contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 31-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 30Aug2022 as dose number unknown, single (Lot number: FP7137) at the age of 31 years for COVID-19 immunization. The patient's relevant medical history was not reported. The patient took concomitant medications. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 2022, outcome "unknown" and all described as "COVID-19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Therapeutic measures were taken as a result of drug ineffective, COVID-19. Clinical course: The patient started Paxlovid on 29Sep2022 and end date not provided for the treatment of COVID-19. Other medications in two weeks were taken by the patient. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 Test; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Exposure to SARS-CoV-2
Incorrect route of product administration
Symptomtext
She was supposed to get the Covid booster bivalent vaccine. She was given the Covid pfizer original vaccine. She hasn't had any adverse reactions but is worried she will get covid because she states over half of her coworkers have covid. She thinks she will die. I explained we contacted Pfizer and it would boost her immune system and we could give her the bivalent vaccine in 2 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exposure to SARS-CoV-2
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- has diabetes
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- Impfdatum
- 05.10.2022
- Beginn
- 05.10.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Wrong product administered
Symptomtext
Patient was administered the primary COVID19 Pfizer -BioNTech vaccine when indicated vaccine should have been COVID19 Pfizer-BioNTech Bivalent. The patient has not reported any adverse effects, only received incorrect Pfizer vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- Impfdatum
- 28.09.2022
- Beginn
- 28.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 29.09.2022
- Beginn
- 29.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
The patient was scheduled to receive the Bivalent booster however received the Monovalent booster in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 05.10.2022
- Impfdatum
- 29.09.2022
- Beginn
- 29.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
The patient was scheduled to receive the Bivalent booster, however received the Monovalent booster in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- Impfdatum
- 29.09.2022
- Beginn
- 29.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
The patient was scheduled to receive the Bivalent booster, however received the Monovalent booster in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- Impfdatum
- 29.09.2022
- Beginn
- 29.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
The patient was scheduled to receive the Bivalent booster however received the Monovalent booster in error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 05.10.2022
- Impfdatum
- 29.09.2022
- Beginn
- 29.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
The patient was scheduled to receive the BiValent booster however received the Monovalent in error
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 04.10.2022
- Impfdatum
- 19.09.2022
- Beginn
- 19.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 04.10.2022
- Impfdatum
- 03.10.2022
- Beginn
- 03.10.2022
- 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
Medication Administration Error. Pfizer monovalent vaccine was administered to patient instead of Pfizer bivalent booster vaccine. The patient was notified of error and was given the option to return to the clinic after 2 months to receive the bivalent booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 02.10.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
NO ADVERSE EVENTS TO NOTE, NO TREATMENT PROVIDED, OUTCOME: N/A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 30.09.2022
- Impfdatum
- 30.09.2022
- Beginn
- 30.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
We administered incorrectly Covid19 Pfizer as a booster instead of Covid19 Pfizer Bi-Valent as a booster...Pt did not exhibit any adverse affects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- DIABETES
- Andere Medikamente
- COUMADIN, LEVOTHYROXINE, JANUVIA,SOLIQUA INSULIN,LIPITOR, IRON, LASIX,GLUCOPHAGE,TOPROL, KDUR,TOUJEO,GLYBURIDE
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 30.09.2022
- Impfdatum
- 23.09.2022
- Beginn
- 23.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
No adverse event
Symptomtext
No Adverse Reaction. Pfizer 12y (+) was given for the 4th dose instead of the Pfizer Bivalent. Our office did not receive the Bivalent injection until 9/21/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 30.09.2022
- Impfdatum
- 16.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
No Adverse Reaction. Pfizer 12y (+) was given for the 4th dose instead of the Pfizer Bivalent. Our office did not receive the Bivalent injection until 9/21/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 28.09.2022
- Impfdatum
- 28.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- -
- Dosis
- UNK
- 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 Mono - Valent Pfizer BNT vaccine instead of newer bivalent vaccine, No other adverse outcome
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 28.09.2022
- Impfdatum
- 28.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient received Mono -Valent Pfizer BNT vaccine instead of newer bivalent booster vaccine, No other adverse outcomes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- diabetes
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 26.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 26.09.2022
- Impfdatum
- 20.09.2022
- Beginn
- 20.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Wrong product administered
Symptomtext
There was a miscommunication on which vaccine the patient wanted. Patient stated they needed their 2nd shot. The staff member entering the patients info took this to mean their 2nd overall dose, but patient was needing their 2nd booster -the new bivalent-. This wasn't noticed until after the shot was given. The patient did not have any adverse reactions, but was upset they have to come back in two months to get the Bivalent shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 23.09.2022
- Beginn
- 23.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Wrong product administered
Symptomtext
Patient was in office for follow up visit where he asked to receive covid booster (Pfizer Bivalent) and flu vaccine. The current employee health nurse was in office for vaccine clinic for employees and had used up the vial of the Bivalent vaccine that was originally opened and handed over fresh vial of vaccine that they had pulled from the vaccine fridge. However this vial was for Pfizer Primary vaccine and not for the Pfizer Bivalent vaccine. Patient was given Pfizer Primary instead of the Bivalent. Mistake was not caught until after vaccine was given and went to document . Provider who had seen patient was notified and has been trying to contact patient to inform them of the incorrect vaccine administration and the next steps.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 23.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
She was supposed to receive Bivalent vaccine for booster, but Comirnaty was given accidently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
He was supposed to receive Bivalent vaccine for booster, but Comirnaty was given accidently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
He was supposed to receive Bivalent COVID booster but received Comirnaty accidently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 23.09.2022
- Impfdatum
- 16.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Vaccination failure
Symptomtext
covid-19; covid-19; This is a spontaneous report received from contactable reporter(s) (Nurse) from product quality group. A 73-year-old male patient received BNT162b2 (BNT162B2), on 07Feb2021 as dose 1, single (Lot number: EM9810), on 01Mar2021 as dose 2, single (Lot number: EN6202), on 24Sep2021 as dose 3 (booster), single (Lot number: 3013SBA), on 30Mar2022 as dose 4 (booster), single (Lot number: FK9894) and on 16Sep2022 as dose 5 (booster), single (Lot number: FP7137) at the age of 73 years for covid-19 immunisation. The patient had no relevant medical history. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "covid-19". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive. Clinical course: Retired registered nurse calling who thought they got the COVID bivalent today but they got a call from the pharmacy where her husband and she went to get it, which was around 3:30 their time. The pharmacy let them know that they had received an old booster dose and not the bivalent. They did tell her, which she was very upset as a nurse herself she doesn't understand how they could make the mistake to give the wrong vaccine, they would have to wait two months to get the bivalent. The only reason they went for vaccine today was for the Omicron booster, and now they have to wait two months, and it is prevalent in the (withheld) area. Caller would like to know if it is a packaging problem, if the bivalent and old booster are packed the same way. Fifth dose was 16Sep2022 of LOT: FP7137, which her card says it was bivalent but it wasn't. Their vaccine cards are handwritten and the only information provided on them was LOT and manufacturer name for each dose, no EXP/NDC. All five doses were Pfizer COVID shots. Caller says she doesn't want to have Omicron, and she thinks it is terrible they went there for getting the booster for Omicron and now have to wait two months, in a medium risk area with back to school. Her grandkids are just getting over COVID, they have been boosted, and she doesn't want to get Omicron because she has seen what the kids have gone through. Her husband had COVID at the beginning of Aug and was very sick. Caller clarifies getting the old booster instead of bivalent is not serious.; Sender's Comments: The efficacy of a drug varies from patient to patient and can be affected by different factors, however a contributory role of the suspect drug BNT162B2 (COMIRNATY) to the reported events Vaccination failure and COVID-19 cannot be ruled out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID 19; Test Result: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: List of non-encoded Patient Relevant History: Patient Other Relevant History 1: None, Comment: Other Conditions: No
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 22.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
Patient didn't have any adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 22.09.2022
- Impfdatum
- 22.09.2022
- Beginn
- 22.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Pt wanted Pfizer bivalent booster, was unintentionally given regular Pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 21.09.2022
- Beginn
- 21.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
No adverse event
Product administration error
Symptomtext
Nurse gave patient PFizer covid shot, NOT the BILVALENT that was ordered by provider. So patient received a 3rd dose of the original covid vaccine and was not able to get his bivalent booster today because of the error. Patient had no adverse effects in the office.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- carnitine deficiency
- Andere Medikamente
- none
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Patient was scheduled for & received a COVID 19 monovalent booster vaccine during the first week of September 2022. During this same week, the CDC published guidance recommending the bivalent booster for 12 years and up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- prilosec pepcid multi vitamin culturelle allegra
- Allergien
- seasonal, not specified
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 21.09.2022
- Impfdatum
- 13.09.2022
- Beginn
- 13.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient was scheduled for and received a COVID-19 Monovalent booster vaccine during the first week of September 2022. During this same week, the CDC published guidance recommending the Bivalent booster vaccine for 12 years and up. The patient's mom (young adult with special needs) was informed about the difference and the option of getting a Bivalent booster in 2 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- CP asthma, moderate persistent developmental delays SVT
- Andere Medikamente
- Baclofen Valium Neurontin Tenormin Atarax Lopressor Kepra Pulmicort nebs Albuterol Nebs
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient was scheduled for and received a COVID-19 Monovalent booster vaccine during the first week of September 2022. During this same week, the CDC published guidance recommending the Bivalent booster vaccine for 12 years and up. The patient was informed about the difference and the option of getting a Bivalent booster in 2 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Asthma, intermittent ADHD anxiety
- Andere Medikamente
- Albuterol MDI Haldol Lithium Synthroid Effexor Vistaril
- Allergien
- Cat & Dog dander Molds
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 20.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Pfizer monovalent given as booster AFTER FDA/CDC removal of EUA for monovalent boosters. Bivalent booster was unavailable at time of administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 20.09.2022
- 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
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. Prevnar 13 v. Prevnar 23)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 20.09.2022
- Impfdatum
- 19.09.2022
- Beginn
- 19.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Interchange of vaccine products
Symptomtext
When screening patient, patient requested to receive Moderna (lot # 011B22A) as her 1st COVID vaccine dose , but received Pfizer (lot # FP7137) primary dose instead. I discussed the mistake with patient after dose given when it was recognized, in which patient reported that she was okay with receiving Pfizer instead, she just wanted to make sure that she was vaccinated. I discussed differences in vaccines and timing differences for 2nd dose primary series. The patient had no questions or concerns.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- None known
- Andere Medikamente
- Pre-natal Vitamins, Iron; others unknown
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 19.09.2022
- Impfdatum
- 16.09.2022
- Beginn
- 16.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none known
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 19.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
8/31/22 ---Emergency Authorization for Pfizer monovalent had been rescinded and as of 9/1/22 only the bivalent was approved for BOOSTER doses. Patient came first thing in the morning before communication had been received by pharmacist from company and the pharmacy did not email until 9:08am on 9/1/22 and the pharmacist had not received that communication either. Patient received vaccination at 9:28am.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 19.09.2022
- Impfdatum
- 16.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
given the monovalent in error should have been bivalent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 19.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Symptomtext
Patient is experiencing issues with numbness in fingers that started about 2 weeks after the vaccine was administered. It is affecting the same arm the vaccine was administered in.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 17.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Circumstance or information capable of leading to medication error
Incorrect product formulation administered
No adverse event
Symptomtext
No known adverse events. Nurse not aware that monovalent vaccine should no longer be used as a COVID booster Dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Circumstance or information capable of leading to medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 17.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
No known adverse events. Nurse not aware that monovalent vaccine should no longer be used as a COVID booster Dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 16.09.2022
- Impfdatum
- 21.01.2021
- Beginn
- 01.09.2022
- Tage bis Beginn
- 588,0
- Dosis
- 4
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abortion induced
Biopsy breast abnormal
Biopsy liver abnormal
Biopsy lymph gland abnormal
Breast mass
Central venous catheterisation
Chemotherapy
HER2 negative breast cancer
Hormone receptor positive breast cancer
Magnetic resonance imaging abnormal
Mammogram abnormal
Metastases to liver
Metastases to lung
Nodule
Positron emission tomogram abnormal
Pregnancy
Pulmonary mass
Ultrasound breast abnormal
Symptomtext
Began noting a breast lump 9/2021 Biopsied ER/PR + HER 2- breast cancer MRI 3/17/2022 with hepatic mets multiple small pulmonary mets also noted. Liver biopsy 4/1/22 consistent with metastatic breast cancer. Noted to be pregnant when she went for port-a-cath. Choose to terminate pregnancy 3/31/22 to allow for complete chemo. ACT 4/5/22-7/23/22 . PET noted resolved axillary nodules and pulmonary nodules, Liver mets responding but still with activity. Sarted Lupron and anastrozole 8/10/22, Kisqoli addes 8/23/22. I am not saying MRNA vaccines caused this but I have seen way more and way younger breast cancer in this remote population in than in a very long career. We have had 18 new cancers since the vaccines only 1 was unvaccinated. This is the youngest ever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abortion induced
- Hospital-Tage
- -
- Labordaten
- Bilateral mammogram and u/s 2/3/22, Breast and axillary biopsy 3/8/22
- Aktuelle Erkrankungen
- Chronic asthma
- Vorgeschichte
- -
- Andere Medikamente
- Albuterol inhaler, Montelukast 10mg, Mometasone/Formoterol
- Allergien
- Fresh Fruits, Hay , Lidocaine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 16.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Medication error
No adverse event
Symptomtext
Patient was given the monovalent vaccine vs the bivalent. no known adverse outcome. We were told by regulatory authority to record this as a med error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 16.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
Patient was given the monovalent vaccine vs the bivalent. no known adverse outcome. We were told DPH to record this as a med error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 16.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
No adverse event
Symptomtext
Patient was given the monovalent vaccine vs the bivalent. no known adverse outcome. We were told by DPH to record this as a med error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 16.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
No adverse event
Symptomtext
Patient was given the monovalent vaccine vs the bivalent. no known adverse outcome. We were told to record this as a med error.
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
- 16.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
No adverse event
Symptomtext
Patient was given the monovalent vaccine vs the bivalent. No known adverse outcome. We were told by local health dept. to record this as a med error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 15.09.2022
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Vial was not refrigerated, and was out of range to use. LPN drew up and administered vaccine to patient. Patient did not suffer ill effects. Provider notified. Manufacturer called and directive was that vaccine was no longer stable, patient will be given booster when scheduled.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN
- Andere Medikamente
- amLODIPine (NORVASC) 2.5 mg tablet hydroCHLOROthiazide 12.5 mg tablet sodium chloride (Muro 128) 5 % ophthalmic solution Vitamin D-3 50 mcg (2,000 unit) capsule
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 15.09.2022
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
Vial was not refrigerated, and was out of range to use. LPN drew up and administered vaccine to patient. Patient did not suffer ill effects. Provider notified. Manufacturer called and directive was that vaccine was no longer stable, patient will be given booster when scheduled.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Cardiovascular NSTEMI (non-ST elevated myocardial infarction) (HC) Endocrine/Metabolic Hyperglycemia Class 2 obesi Cardiovascular NSTEMI (non-ST elevated myocardial infarction) (HC) Endocrine/Metabolic Hyperglycemia Class 2 obesity without serious comorbidity with body mass index (BMI) of 36.0 to 36.9 in adult Type 2 diabetes mellitus without complication, without long-term current use of insulin (HC) Gastrointestinal Gastroesophageal reflux disease without esophagitis Sigmoid diverticulosis Musculoskeletal Closed fracture of shaft of right ulna Sternal manubrial dissociation, initial encounter for closed fracture Multiple closed fractures involving both upper extremities with rib and sternum Fracture of thoracic transverse process, closed, initial encounter (HC) Fracture of distal radius and ulna, left, closed, initial encounter Closed avulsion fracture of shaft of metacarpal bone Closed displaced spiral fracture of shaft of right ulna Neurology Neuropathy Respiratory Acute respiratory failure with hypoxia (HC)
- Andere Medikamente
- acetaminophen (TYLENOL EXTRA STRGTH) 500 mg tablet amitriptyl acetaminophen (TYLENOL EXTRA STRGTH) 500 mg tablet amitriptyline (ELAVIL) 75 mg tablet aspirin chewable 81 mg chewable tablet atorvastatin (LIPITOR) 80 mg tablet famotidine
- Allergien
- Gabapentin
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 14.09.2022
- Impfdatum
- 23.08.2022
- Beginn
- 23.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Adult dose for ages 12+ given to child age 11
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 13.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 08.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
ADMINISTRATION ERROR (WAS GIVEN MONOVALENT PFIZER COVID VACCINE as BOOSTER)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CHRONIC KIDNEY DISEASE
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect product formulation administered
Symptomtext
ADMINISTRATION ERROR (WAS GIVEN PFIZER MONOVALENT VACCINE)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 13.09.2022
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
ADMINISTRATION ERROR ( WAS GIVEN A MONOVALENT PFIZER VACCINE for BOOSTER)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 13.09.2022
- Impfdatum
- 10.09.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Original pfizer was given instead of bivalent. CDC recommended no course of action needed may receive bivalent in 2 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 09.09.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.09.2022
- Impfdatum
- 09.09.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Patient was given booster after EUA ended for Pfizer booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 12.09.2022
- Beginn
- 12.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
pt was to get the booster / third shot . she rec'd the monochromal pfizer . according to cdc guidelines all boosters are to be bivalent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none/unknown
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 10.09.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient received original pfizer formulation instead of bivalent. CDC recommended no action may receive bivalent in 2 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 10.09.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient received original pfizer formulation instead of bivalent. CDC recommended no action may receive bivalent in 2 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 10.09.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient received original pfizer formulation instead of bivalent. CDC recommended no action may receive bivalent in 2 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 10.09.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Patient received original pfizer formulation instead of bivalent. CDC recommended no action may receive bivalent in 2 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 10.09.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient received original pfizer formulation instead of bivalent. CDC recommended no action may receive bivalent in 2 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 12.09.2022
- Impfdatum
- 10.09.2022
- Beginn
- 10.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Patient received pfizer original formulation versus bivalent. CDC recommended no action needed and bivalent dose can be given in 2 months
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 09.09.2022
- Impfdatum
- 09.09.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
pt given monovalent covid vaccine instead of bivalent booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- na
- Andere Medikamente
- na
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Medication error
Symptomtext
MEDICATION ERROR
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Medication error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 09.09.2022
- Impfdatum
- 02.09.2022
- Beginn
- 02.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Symptomtext
MEDICATION ERROR
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 09.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Symptomtext
MEDICATION ERROR
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 09.09.2022
- Impfdatum
- 09.09.2022
- Beginn
- 09.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Patient 12 years of age or older who received the original mRNA formulation (aka monovalent formulation) as a booster dose. Due to the FDA's abrupt revision of booster recommendations means that administering the monovalent to individuals 12 years of age or older is considered a medication error as of 8/31/2022 and been advised that a VAERS be completed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 08.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Product administered to patient of inappropriate age
Symptomtext
Patient reported feeling fine when leaving the pharmacy after monitoring for 20 mins. However the 9 year old patient received an adult dose of the Pfizer biotech vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 08.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Symptomtext
No symptoms noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Per the recommendations of our local health jurisdiction, we are reporting this as an adverse event, since the booster was given after the FDA unauthorized the use of monovalent vaccines as booster doses for individuals 12 years of age and older.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 07.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Per the recommendations of our local health jurisdiction, we are reporting this as an adverse event as the booster was given after the FDA unauthorized the use of monovalent vaccines as booster doses for individuals 12 years of age and older.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE LISTED
- Andere Medikamente
- UNKNOWN
- Allergien
- YES, BUT NO SPECIFICATION AS TO WHAT
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Per the recommendations of our local health jurisdiction, we are reporting this as an adverse event as the booster was given after the FDA unauthorized the use of monovalent vaccines as booster doses for individuals 12 years of age and older.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 07.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Per the recommendations of our local health jurisdiction, we are reporting this as an adverse event as the booster was given after the FDA unauthorized the use of monovalent vaccines as booster doses for individuals 12 years of age and older.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 07.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Per the recommendations of our local health jurisdiction, we are reporting this as an adverse event as the booster was given after the FDA unauthorized the use of monovalent vaccines as booster doses for individuals 12 years of age and older.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 07.09.2022
- Impfdatum
- 31.08.2022
- Beginn
- 31.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Per the recommendations of our local health jurisdiction, we are reporting this as an adverse event as the booster was given after unauthorized the use of monovalent vaccines as booster doses for individuals 12 years of age and older.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 02.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
No adverse event
Symptomtext
no adverse reaction, monovalent booster given end date of monovalent booster doses
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 02.09.2022
- Impfdatum
- 01.09.2022
- Beginn
- 01.09.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect product formulation administered
Symptomtext
Patient was given Pfizer monovalent vaccine as a first booster on 9/1/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 31.08.2022
- Impfdatum
- 15.08.2022
- Beginn
- 18.08.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Pt tested positive for COVID on 08/18/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 31.08.2022
- Impfdatum
- 29.08.2022
- Beginn
- 29.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Wrong product administered
Symptomtext
Our pharmacy intern incorrectly administered a fifth dose of Pfizer (12+) to patient on 8/29/2022. The patient was expecting to receive a high-dose flu vaccine. No reported adverse event as of 8/31/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 27.08.2022
- Impfdatum
- 20.08.2022
- Beginn
- 27.08.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoacusis
Tinnitus
Symptomtext
Tinnitis and decreased hearing in L ear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoacusis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- multivitamin
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 26.08.2022
- Impfdatum
- 22.08.2022
- Beginn
- 22.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Error: Dose in series given too early.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 25.08.2022
- Impfdatum
- 24.08.2022
- Beginn
- 25.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
NA - vaccine was punctured 8/23 1410. Vaccine was administered 8/24 around 1404
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- Diabetes type 1
- Andere Medikamente
- Enskyce, vitamin D2, Novolog, Tresiba, lisinopril
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 24.08.2022
- Impfdatum
- 17.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
No adverse event
Symptomtext
He had received a dose of Moderna vaccine on 10/08/2022 at local Regional Medical Center, then he returned to same clinic on 08/17/2022 he presented a vaccine card that only had a 1st dose Pfizer listed that had received from local pharmacy on 07/05/2022. Therefore, he was given what according to his card would be his 2nd Pfizer vaccine. It was not until I entering into tracking system that noted documentation of the 1st dose being Moderna on 10/08/2021 and a 2nd dose of Pfizer on 07/05/2022. I have reached out to the nurse that administered the vaccine and she informed me that he only presented with 1 vaccine card with Pfizer and told her was his 2nd vaccine and completed a consent for 2nd dose of Pfizer. Nurse voiced when she contacted him 08/23/2022 when I noted that had received 2 different vaccines and he denied being aware of the first vaccine back on 10/08/2021 but we have a consent form that he signed for this vaccine. He denied having any side effects from the vaccine received 08/17/2022. I did notify Nurse that as vaccine on 08/17/2022 was only 6 weeks after 2nd vaccine that could not consider as a booster dose as had to be at least 5 months, so he would need to receive another vaccine in 5 months for his booster dose and she would let him know. We do have a signed consent from his both vaccines that received. I did contact local pharmacy and there he completed consent that was his first vaccine on 07/05/2022 and was given Pfizer vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 24.08.2022
- Impfdatum
- 23.08.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
No adverse events noted, patient reports she feels fine.. Given at 9:30am on 8/23/22, drawn up on 8/22/22 at 8:40am. Spoke to Pfizer and they stated since administer time exceeded 24 hours, may not be as effective. Referred to site for further guidance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- DM II, CHF, bilateral coronary artery stenosis, essential HTN, hearing impairment, seizures, hypothyroidism, osteopenia, vision impairment right eye, thrombocytosis, HLD, choroidal nevus of left eye, abnormal mammogram, falls
- Andere Medikamente
- Amlodipine 10mg daily, atorvastatin 80mg daily, levothyroxine 50mcg daily, lisinopril 40mg daily, metformin 1000mg BID, aspirin 81mg daily
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 18.08.2022
- Impfdatum
- 16.08.2022
- Beginn
- 17.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast swelling
Swelling
Tenderness
Symptomtext
Day after large swelling in R upper outer quadrant of breast/ upper chest wall, tender, swollen, no redness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast swelling
- Hospital-Tage
- -
- Labordaten
- ordered ultrasound which is pending
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- metformin, provera
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 16.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 11,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Intermenstrual bleeding
Symptomtext
Starting Friday, Aug 12th, I had breakthrough menstrual bleeding. It's a moderate flow and is still continuing. Today is day 5. I have not had any heavy bleeding for about 3-4 months. I had a uterine ablation in October of 2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intermenstrual bleeding
- Hospital-Tage
- -
- Labordaten
- I have not had any medical tests complete.
- Aktuelle Erkrankungen
- I was not experiencing any illness.
- Vorgeschichte
- I have psoriasis.
- Andere Medikamente
- I was taking a multivitamin and a probiotic.
- Allergien
- I am allergic to cephalexin.
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 16.08.2022
- Impfdatum
- 12.08.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Oropharyngeal discomfort
Symptomtext
Male patient of 73 years of age, oriented in time, place and person. Reports feeling discomfort in the throat area. Vital Signs Pulse: 78, B/P 140/80 Spo2 98%, Dextrose: 119. Consultation is made with the Medical Director, who indicates that she be administered Benadryl and Tylenol at 3:17pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal discomfort
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Metropolol
- Allergien
- Aspirin
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 14.08.2022
- Impfdatum
- 10.08.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 13.08.2022
- Impfdatum
- 11.08.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Peripheral swelling
Symptomtext
PATIENT CAME IN ON 8/11/2022 TO GET THE BOOSTER DOSE OF COVID19 VACCINE . PATIENT HAD COMPLETED THE PRIMARY SERIES WITH MODERNA BUT WANTED TO SWITCH TO PFIZER THIS TIME. SHE WAS VACINATED AT 10:38 AM ON THE RIGHT ARM INTRAMUSCULARLY WITH 0.3 ML OF PFIZER LOT #FP7137. PATIENT REPORTED 24 HOURS LATER ON THE NEXT DAY IN THE MORNING, HER UNDERARM WAS SWOLLEN BUT SAID THERE WAS NO FEVER OR PAIN OR WARM SENSATION. SHE FEELS OKAY BUT JUST A BIT UNCOMFORTABLE ABOUT THE SWELLING AS SHE COULD FEEL IT. I TOLD HER TO TAKE SOME ANTI-INFLAMATORY DRUG AND USE ICE TO ALLEVIATE THE SWELLING AND LET US KNOW IF IT GETS BETTER. PATIENT SAID OKAY AND LEFT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discomfort
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 12.08.2022
- Impfdatum
- 12.08.2022
- Beginn
- 12.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient received 2nd booster; does not meet eligibility requirements.. Monitored for 15 minutes; departed clinic s/s adverse reaction. Patient updated of unauthorized dose. Stated, "I thought this was my first booster"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HLD, Etoh above recommended consumption, glucose-6-phosphate-dehydrogenase deficiency
- Andere Medikamente
- none
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 12.08.2022
- Impfdatum
- 30.07.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inflammation
Symptomtext
Patient refers that two days after receiving her second booster dose of Pfizer vaccine she experience inflammation under the arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inflammation
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- Thyroid.
- Andere Medikamente
- NO
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 11.08.2022
- Impfdatum
- 10.08.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Patient received a 5th dose of Pfizer vaccine. Vaccination card not available at appointment. Pharmacy records showed only 3 previous doses given at facility. First COVID-19 vaccination given at a different facility per records. Previous Pfizer booster given 3/11/2022 at our facility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 11.08.2022
- Impfdatum
- 07.08.2022
- Beginn
- 07.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Error: Dose in Series Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 10.08.2022
- Impfdatum
- 10.08.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event reported however dose given as 2nd booster was expired at time of administration. Vial was pulled from the refrigerator on 8/9/22 10:47Am. Dose given from that vial on 8/10/22 2:31pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 10.08.2022
- Impfdatum
- 05.08.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Symptomtext
Patient states that she developed reddness on her face. not itchy no trouble breathing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 09.08.2022
- Impfdatum
- 05.08.2022
- Beginn
- 05.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Wrong product administered
Symptomtext
Error: Wrong Vaccine/Product Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 08.08.2022
- Impfdatum
- 08.08.2022
- Beginn
- 08.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient was given a 4th dose of COVID. No adverse reactions at the time of the event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 08.08.2022
- Impfdatum
- 01.08.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
no adverse events Patient received fifth dose of current four dose series
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 08.08.2022
- Impfdatum
- 03.08.2022
- Beginn
- 03.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Error: Dose in Series Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 05.08.2022
- Impfdatum
- 28.07.2022
- Beginn
- 29.07.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood urine present
Symptomtext
Blood in urine; This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 64-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 28Jul2022 at 15:00 as dose 3 (booster), single (Lot number: FP7137) at the age of 64 years, in left arm for covid-19 immunisation. The patient's relevant medical history included: "NHL Lymphoma" (unspecified if ongoing); "CVID" (unspecified if ongoing); "Known allergies: Sulfa" (unspecified if ongoing); "Covid-19" (unspecified if ongoing). The patient took concomitant medications. Vaccination history included: BNT162b2 (Prev dose product=COVID 19, Prev dose brand=Pfizer Biontech, Prev dose brand unknown=False, Prev dose lot unknown=True, Prev dose lot unknown reason=Unable to locate or read the details, Prev dose administration time=12:00 AM, Prev dose number=2, Prev dose vaccine location=Left arm), administration date: 28Apr2021, when the patient was 63-year-old, for COVID-19 immunization; BNT162b2 (Prev dose product=COVID 19, Prev dose brand=Pfizer Biontech, Prev dose brand unknown=False, Prev dose lot number=EW0151, Prev dose lot unknown=False, Prev dose administration time=12:00 AM, Prev dose number=1, Prev dose vaccine location=Left arm), administration date: 07Apr2021, when the patient was 63-year-old, for Covid-19 immunization. The following information was reported: BLOOD URINE PRESENT (medically significant) with onset 29Jul2022 at 19:00, outcome "unknown", described as "Blood in urine". The event "blood in urine" required physician office visit. The patient underwent the following laboratory tests and procedures: Blood urine present: (29Jul2022) Blood in urine. It was unknown if therapeutic measures were taken as a result of blood urine present. The patient did not receive any other vaccines within four weeks prior to the vaccination. Other medications in two weeks were too long to list. Prior to vaccination, the patient was not diagnosed with COVID-19. Since the vaccination, the patient had not been tested for COVID-19. No follow-up attempts are possible. No further information is expected.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood urine present
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220729; Test Name: Blood in urine; Result Unstructured Data: Test Result:Blood in urine
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Common variable immunodeficiency; COVID-19; Non-Hodgkin's lymphoma; Sulfonamide allergy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 02.08.2022
- Impfdatum
- 02.08.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Inappropriate schedule of product administration
No adverse event
Symptomtext
Pt was given what was believed to be the 2nd COVID booster today. After administration patient found vax card and turns out that she was given the 2nd booster on 5/18/22 and reimmunized today as the 2nd covid booster was not documented on the EMR or internet site. After looking back in her chart, she did have an appt for 2nd booster and consent was signed. Pt notified of event. No adverse reactions observed while patient was in the clinic 15 minutes post vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 31.07.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product preparation issue
Symptomtext
Error: Incorrect Reconstitution-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product preparation issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 9,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 26.07.2022
- Beginn
- 01.07.2022
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
The Pfizer 12Y and up vaccine was administered rather than the 5-11Y vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 22.07.2022
- Beginn
- 22.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Client given second booster dose of Pfizer Covid 19 vaccine with no accompanying immunocompromising condition noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Asthma
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MP
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 19.07.2022
- Beginn
- 19.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Patient insisted on getting 1st booster dose (07/19/2022) although just vaccinated for 2nd dose only 3 days ago (07/16/2022) stating that they needed a booster to be able to travel.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Pfizer COVID-19 Vaccine
- Allergien
- None
- Vorherige Impfungen
- -