- Staat
- -
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 07.11.2023
- Impfdatum
- 15.01.2022
- Beginn
- 05.11.2023
- Tage bis Beginn
- 659,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain
Alanine aminotransferase increased
Angiogram normal
Angiogram pulmonary normal
Anion gap
Aspartate aminotransferase increased
Asthenia
Back pain
Bacterial test positive
Basophil count decreased
Basophil percentage decreased
Bilirubin urine
Blood albumin decreased
Blood alkaline phosphatase increased
Blood bilirubin normal
Blood calcium decreased
Blood chloride normal
Blood creatinine normal
Symptomtext
Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on November 05, 2023 20:35 EST Verified By: MD on November 05, 2023 20:35 EST Encounter Info: Hospital, Inpatient, 11/05/23 - * Final Report * Chief Complaint Abdomen pain History of Present Illness/Subjective 36-year-old female with past medical history COPD here with diffuse abdomen painx3 days of mild of moderate severity, radiating to the back, no relieving or exacerbating factors. Reports fever to 101. Also complaining of generalized weakness and malaise. Denies nausea, vomiting, abdomen pain.No shortness of air or diaphoresis. Does report a mild cough productive of scant amounts of white sputum with some pleuritic chest pain. White blood cell count 14,000, increased absolute neutrophil count.Mildly elevated D-dimer. Potassium 2.8, alkaline phosphatase 164, minimal elevation of AST and ALT, total bilirubin is normal, she has prior cholecystectomy. Serum lactate is 0.7, cardiac enzymes are negative. Urine shows bacteria, pyuria ,microhematuria, nitrite positivity. COVID-19 positive as well. Normotensive with mean arterial pressure in the 70s but systolic blood pressure on the soft side in the high 90s and low 100s. Mildly tachycardic.No hypoxia. CT of the abdomen pelvis shows decreased cortical perfusion in a patchy distribution as well as perinephric stranding bilaterally. CT angiography shows no acute abnormality including pulmonary embolus. Review of Systems Complains of mild nonproductive cough, pleuritic chest pain, fever,abdomen pain. Denies shortness of air. No nausea vomiting or diarrhea hematochezia or melena. Remaining 10 point review of systems negative except as noted above. Physical Exam/Objective Vitals & Measurements most recent past 24 hours T: 37.5 ?C (Oral) BP: 98/65 HR: 112 (Monitored) HR: 110 (Peripheral) RR: 17 SpO2: 96% Oxygen Therapy: Room air WT: 50.30 kg (WFC) Hemodynamics Neurologic Glasgow Coma Score: 15 Patient Weight Current Daily Weight: 50.3 kg 11/05/23 Patient Height Current Height: 162.6 cm 11/05/23 Constitutional: No acute distress, well-nourished Eyes: PERRLA, EOMI, normal conjunctiva ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: Lungs CTAB Cardiovascular: Regular rate and rhythm Gastrointestinal: Soft, non-tender, non-distended Musculoskeletal: No joint swelling, no deformity, bilateral CVA tenderness to palpation Integumentary: Intact, warm, dry no rashes Neurologic: Alert & Oriented x 3, no cognitive impairment, no focal deficits Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan 1. Acute pyelonephritis N10 The patient has no multidrug-resistant risk factors thus will prescribe ceftriaxone 1 g every 24 hours, pain control, as needed antiemetics, follow cultures, follow procalcitonin levels. 2. COVID-19 virus infection U07.1 Not sure we can call this asymptomatic with fever, however, no hypoxia. Supportive care. 3. Sepsis A41.9 Present on admission secondary to urinary tract infection. Follow bolus guidelines and then administer maintenance IV fluids to maintain a mean arterial pressure of 65 and urine output of 50 mL/h. Recheck on physical examination shows appropriate capillary refill and peripheral tissue perfusion. We will follow urine and blood cultures. Antibiotics as described above. This is a urinary tract infection in a young female with nitrite positivity, no indication for gram-positive coverage at this point. 4. Elevated liver enzymes R74.8 Chronic, stable, follow 5. Hypokalemia E87.6 Replete and follow Orders: albuterol, 2 Puff, Inhalation, MDI/DPI Inhaler Treatment, 4 Times Daily, 11/05/23 21:00:00 EST Sodium Chloride 0.9% 500 mL, Total Volume (mL) = 500, IV Continuous, 11/05/23 19:50:00 EST, Other - See Comments, Clinical Weight Sodium Chloride 0.9% 500 mL, Total Volume (mL) = 500, IV Continuous, 11/05/23 19:50:00 EST, Other - See Comments, Clinical Weight Full code Lovenox Code Status Full Code Chronic Problem List Extensive tattoos History of conization of cervix History of depression History of migraine headaches Request for sterilization Procedure/Surgical History ?Laparoscopic cholecystectomy (01/11/2023) ?Oral surgery (02/2016) ?Pap smear for cervical cancer screening.... (06/16/2015) ?Colposcopy (06/09/2006) ?Abnormal pap smear (03/07/2006) ?Extraction of wisdom tooth (2003) ?Conization of uterine cervix (12/18/2001) ?cholesystectomy Surgical History Internal 01/11/2023 Cholecystectomy Laparoscopic MD 08/14/2020 Tubal Ligation Laparoscopic MD Medications Home Medications (3) Active Benadryl 25 mg oral tablet 25 mg = 1 Tablet, PRN, Orally, At Bedtime Ventolin HFA 90 mCg/inh inhalation aerosol 180 mCg = 2 Puff, Inhalation, 4 Times Daily, May use up to 3-4 puffs four times a day. Wixela Inhub 500 mCg-50 mCg inhalation powder , Inhalation, BID Active Scheduled Inpatient Medications albuterol (Albuterol (Eqv-Ventolin HFA) 90 mCg/inh inhalation aerosol), Aerosol, 2 Puff, Inhalation, 4 Times Daily, Start: 11/05/23 21:00:00 potassium chloride (potassium chloride extended release), Tab, Extended Rel, 20 mEq, Orally, ONCE, Start: 11/05/23 17:00:00 Sodium Chloride 0.9% 500 mL IV Continuous Other - See Comments Sodium Chloride 0.9% 500 mL IV Continuous Other - See Comments One-Time Medications Given 11/04/23 00:00:00 TO 11/05/23 20:34:49 ceftRIAXone, Injection, 1 GM, IV Push, ONCE, (1 DOSE 11/05/23 16:02:00) HYDROmorphone (HYDROmorphone Inj ED (1 mg/mL)), Injection, 1 mg, IV Push, ONCE, (1 DOSE 11/05/23 15:06:00) ondansetron, Injection, 4 mg, IV Push, ONCE, prn, Nausea/Vomiting IV - Use First, (1 DOSE 11/05/23 15:06:00) Sodium Chloride 0.9% (Sodium Chloride 0.9% - ED Bolus), Infusion, 500 mL, IVPB, ONCE, (1 DOSE 11/05/23 15:04:00) Sodium Chloride 0.9% (Sodium Chloride 0.9% - ED Bolus), Infusion, 1,000 mL, IVPB, ONCE, (1 DOSE 11/05/23 18:09:00) Sodium Chloride 0.9% (Sodium Chloride 0.9% - ED Bolus), Infusion, 1,000 mL, IVPB, ONCE, (1 DOSE 11/05/23 18:09:00) PRN Medications (0600 - 0559) from 11/04 - 11/05 HYDROmorphone, 1 mg, IV Push, Q10min, 0 Dose(s) Allergies morphine (Itching, Hives) Social History Alcohol Denies Electronic Cigarette/Vaping E-Cigarette Use Never. Employment/School Employed, Work/School description: GM x 10 years. Highest education level: Some college. Home/Environment (Married, has been together since 2013), Lives with Children, Spouse. Nutrition/Health Diet: Regular. Other Sexual Sexually active: Yes. History of sexual abuse: Yes. Other sexual concerns: Pt states she was sexually abused at age 10 by brother's friend. She states her first husband was physically abusive. ACE Score-5 Declines any counseling at present. States she had counseling in the past.. Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History Alcoholism /alcohol abuse...: Mother and Father. Anxiety: Mother. Blood clot: Aunt. Breast cancer: Grandmother (M). COPD (chronic obstructive pulmonary disease)...: Mother. DVT (deep venous thrombosis)....: Aunt. Depression: Mother. Drug abuse: Father and Brother. Drug dependency...: Brother. Hepatitis c, chronic...: Father. Hypertension: Mother. Hypertension..: Father. Lung cancer..: Grandfather (P). Migraines..: Mother. Miscarriage: Mother. Myocardial infarction...: Grandfather (M). Rheumatoid arthritis: Mother. Skin cancer: Grandfather (M). Grandmother (P): History is negative Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 14.4 k/cumm High (11/05/23 14:51:00) RBC: 3.4 million/cumm Low (11/05/23 14:51:00) Hgb: 10.1 GM/dL Low (11/05/23 14:51:00) Hct: 29.7 % Low (11/05/23 14:51:00) MCV: 88 fL (11/05/23 14:51:00) MCH: 29.6 pg (11/05/23 14:51:00) MCHC: 33.9 GM/dL (11/05/23 14:51:00) RDW: 13.7 % (11/05/23 14:51:00) Platelet: 238 k/cumm (11/05/23 14:51:00) MPV: 8 fL (11/05/23 14:51:00) Neutrophils %: 84 % (11/05/23 14:51:00) Lymphocytes %: 4 % (11/05/23 14:51:00) Monocytes %: 12 % (11/05/23 14:51:00) Eosinophils %: 0 % (11/05/23 14:51:00) Basophils %: 0 % (11/05/23 14:51:00) Absolute Neutrophil: 12.1 k/cumm High (11/05/23 14:51:00) Absolute Lymphocyte: 0.5 k/cumm Low (11/05/23 14:51:00) Absolute Monocyte: 1.8 k/cumm High (11/05/23 14:51:00) Absolute Eosinophil: 0 k/cumm (11/05/23 14:51:00) Absolute Basophil: 0 k/cumm (11/05/23 14:51:00) Chemistry: Sodium SerPl QN: 138 mmol/L (11/05/23 14:51:00) Potassium SerPl QN: 2.8 mmol/L Critical (11/05/23 14:51:00) Chloride SerPl QN: 103 mmol/L (11/05/23 14:51:00) Carbon Dioxide SerPl QN: 24 mmol/L (11/05/23 14:51:00) Anion Gap: 11 mmol/L (11/05/23 14:51:00) BUN SerPl QN: 12 mg/dL (11/05/23 14:51:00) Creatinine SerPl QN: 0.84 mg/dL (11/05/23 14:51:00) Estimated GFR (CKD-EPI, no race): >90 (11/05/23 14:51:00) Estimated CRCL (CG): 74 mL/min (11/05/23 14:51:00) Glucose SerPl QN: 93 mg/dL (11/05/23 14:51:00) Calcium Total SerPl QN: 8.2 mg/dL Low (11/05/23 14:51:00) Alkaline Phos SerPl QN: 164 Units/L High (11/05/23 14:51:00) ALT SerPl QN: 75 Units/L High (11/05/23 14:51:00) AST SerPl QN: 53 Units/L High (11/05/23 14:51:00) Bilirubin Total SerPl QN: 1 mg/dL (11/05/23 14:51:00) Total Protein SerPl QN: 6.4 GM/dL (11/05/23 14:51:00) Albumin SerPl QN: 3.4 GM/dL Low (11/05/23 14:51:00) Lipase SerPl QN: 12 Units/L (11/05/23 14:51:00) Troponin-I High Sensitivity: 7 ng/L (11/05/23 15:57:00) Lactate Venous Pl QN: 0.7 mmol/L (11/05/23 14:51:00) Coagulation: D-Dimer Pl QN: 304 ng/mL DDU High (11/05/23 14:51:00) Urine Studies: Pregnancy Test Urine: Negative (11/05/23 14:34:00) Color: Yellow (11/05/23 14:34:00) Clarity: Slightly Cloudy (11/05/23 14:34:00) Specific Gravity: 1.022 (11/05/23 14:34:00) pH: 6 (11/05/23 14:34:00) Protein: 100 Abnormal (11/05/23 14:34:00) Glucose: Normal (11/05/23 14:34:00) Ketones: 20 Abnormal (11/05/23 14:34:00) Bilirubin: NEGATIVE (11/05/23 14:34:00) Hgb Ur: TRACE. Abnormal (11/05/23 14:34:00) Nitrite: Positive 2+ Abnormal (11/05/23 14:34:00) Urobilinogen: 2.0 2 Abnormal (11/05/23 14:34:00) Leukocyte Esterase Ur: Large500 Abnormal (11/05/23 14:34:00) WBC: >100 Abnormal (11/05/23 14:34:00) RBC: 11-20 Abnormal (11/05/23 14:34:00) Bacteria: Many Abnormal (11/05/23 14:34:00) Squamous Epithelial: Few (11/05/23 14:34:00) Mucous: PRESENT. (11/05/23 14:34:00) Hyaline Casts: 3-5 (11/05/23 14:34:00) All Other Labs: COVID 19 Specimen Source: Nasal (11/05/23 14:34:00) Coronavirus SARS-CoV2 Rapid: Detected Abnormal (11/05/23 14:34:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (11/05/23 14:34:00) Rapid Influenza A PCR: Not Detected (11/05/23 14:34:00) Rapid Influenza B PCR: Not Detected (11/05/23 14:34:00) Diagnostics Radiology Results - Last 24 hours Across Visits 11/05/2023 16:55 - CTA Abd/Pelvis WO/W IV Contrast IMPRESSION:1. Negative for aortic dissection.2. Findings most consistent with RIGHT worse than LEFTpyelonephritis. No evidence of ureteral obstruction.3. Small volume free fluid in the pelvis may be physiologic in areproductive age female.4. Borderline splenomegaly.Thank you for consulting our team of subspecialty radiologists at Physicians Radiology. 11/05/2023 16:55 - CTA Chest WO/W IV Contrast IMPRESSION:1. No acute findings in the chest. Abdominopelvic findings reportedseparately.Thank you for consulting our team of subspecialty radiologists at Physicians Radiology. Signature Line Electronically Signed on 11/05/23 20:35 EST ________________________________________________________ MD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Coma scale
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 09.08.2023
- Impfdatum
- 14.01.2022
- Beginn
- 12.01.2023
- Tage bis Beginn
- 363,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cerebral artery occlusion
Cerebrovascular accident
Reversible ischaemic neurological deficit
Symptomtext
ACUTE STROKE DUE TO OCCLUSION OF LEFT MIDDLE CEREBRAL ARTERY REVERSIBLE ISCHEMIC NEUROLOGIC DEFICIT SYNDROME
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 08.08.2023
- Impfdatum
- 02.02.2022
- Beginn
- 23.01.2023
- Tage bis Beginn
- 355,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptom recurrence
Symptomtext
ACUTE RESPIRATORY FAILURE 1/30/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 21.07.2023
- Impfdatum
- 31.01.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 226,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
Acute respiratory failure
Aortic arteriosclerosis
Colitis
Symptomtext
ACUTE NON ST ELEVATION MI 4/24/2023 COLITIS ACUTE HYPOXEMIC RESPIRATORY FAILURE 4/24/2023 COLITIS ACUTE NON ST ELEVATION MI 4/24/2023 ATHEROSCLEROSIS OF AORTA ACUTE HYPOXEMIC RESPIRATORY FAILURE 4/24/2023 ATHEROSCLEROSIS OF AORTA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 14.06.2023
- Impfdatum
- 25.01.2022
- Beginn
- 21.12.2022
- Tage bis Beginn
- 330,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute myocardial infarction
Symptomtext
ACUTE NON ST ELEVATION MI ACUTE MI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 22.05.2023
- Impfdatum
- 30.12.2021
- Beginn
- 05.06.2022
- Tage bis Beginn
- 157,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Blood culture negative
COVID-19
Chronic kidney disease
Condition aggravated
Constipation
Encephalopathy
Endotracheal intubation
Essential hypertension
Hyperlipidaemia
Hypotension
Intensive care
Mechanical ventilation
Pancreatic disorder
Pleural effusion
SARS-CoV-2 test positive
Senile dementia
Septic shock
Symptomtext
BREAKTHROUGH COVID: PT FULLY VACCINATED. 85-year-old female admitted to intensive care unit during a septic shock, necessitating mechanical ventilation and vasopressors for the 1st 48 hours of the hospitalization, when she was extubated successfully and vasopressors were able to be discontinued, antibiotic therapy with fosfomycin and doxycycline. Subsequent blood cultures follow-up were negative. Patient diagnosed with COVID 19 infection, possible the triggered the acute respiratory failure necessitating mechanical ventilation at the time of admission. Patient was treated with Decadron, as well as with 5 days of remdesivir, which she completed both treatments here in the hospital. On June 16th patient was considered non infectious and will be able to transition to the skilled nurse facility. Primary Discharge Diagnosis: Acute Hypoxemic Respiratory Failure, requiring intubation. Extubated 6/7, COVID-19 Positive, Bilateral Pleural Effusions,Severe sepsis with shock, Acute encephalopathy secondary to sepsis, Senile Dementia, Nonspecific radiographic changes on pancreas, Chronic kidney disease, Essential hypertension, Hypotension upon admission, Hyperlipidemia, AND Constipation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 13,0
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- DEMENTIA, Chronic kidney disease, ESSENTIAL HYPERTENSION,
- Andere Medikamente
- UNKNOWN
- Allergien
- EGGS
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 19.05.2023
- Impfdatum
- 04.02.2022
- Beginn
- 18.10.2022
- Tage bis Beginn
- 256,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Pneumonia
Symptomtext
ACUTE HYPOXEMIC RESPIRATORY FAILURE 10/18/2022 PNEUMONIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 02.05.2023
- Impfdatum
- 22.01.2022
- Beginn
- 05.06.2022
- Tage bis Beginn
- 134,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Hypoxia
Respiratory failure
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE RESPIRATORY FAILURE RESPIRATORY FAILURE, UNSPECIFIED ACUITY HYPOXIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 01.05.2023
- Impfdatum
- 01.02.2022
- Beginn
- 18.07.2022
- Tage bis Beginn
- 167,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE RESPIRATORY FAILURE HYPOXIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 14.09.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 42,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Hypoxia
Symptomtext
ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 05.12.2022
- Impfdatum
- 07.04.2022
- Beginn
- 21.09.2022
- Tage bis Beginn
- 167,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Death
Decreased appetite
Fatigue
Hypoxia
Malaise
Oropharyngeal pain
Pneumonia
Pyrexia
SARS-CoV-2 test positive
Unresponsive to stimuli
Vaccine breakthrough infection
Symptomtext
This is an instance of breakthrough COVID-19 disease after which death occurred. The individual was vaccinated with the Moderna product on 03/04/2021, 04/01/2021, 11/11/2021, and 04/07/2022. They first tested positive via antigen test at the long term care facility at which they were a resident on 09/21/2022. They presented to emergency department on 09/25/2022 with sore throat, fever, malaise, decreased appetite, and fatigue. They were admitted to hospital and found to have bronchopneumonia and to be hypoxic. They were discharged back to the long term care facility on 09/28/2022. They then presented to emergency department on 10/10/2022 with a chief complaint of "a brief episode of unresponsiveness while eating" which was possibly attributed to choking. They were discharged back to the long term care facility, on hospice on 10/11/2022. They were seen by the LTCF provider on 10/12/2022 and hospice status was confirmed. They died on 10/17/2022. Even with the length of time between the positive COVID-19 test and the death, COVID-19 is on the death certificate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 8,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Type II Diabetes, Dyslipidemia, Vascular Dementia, Hypertension The individual was a resident of the long-term care facility indicated in the Address portion of this form.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 08.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 6,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute kidney injury
Death
Morganella infection
Proteus infection
Symptomtext
DEATH N17.9 - Acute kidney failure, unspecified B96.4 - Proteus (mirabilis) (morganii) as the cause of diseases classified elsewhere
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 27.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Agonal respiration
COVID-19
Death
Endotracheal intubation
Loss of consciousness
Mental status changes
Pulse absent
Resuscitation
SARS-CoV-2 test positive
Symptomtext
pt brought to ED (Hospital) via EMS; pt lost consciousness while transferring to bed at home; acute change in mental status; pt with agonal respirations; positive for COVID; intubated then found to be pulseless; CPR but no rhythm ever obtained; pt passed away in the ED; pt received COVID booster vaccine the day before her death.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Anemia, COPD, DM, HTN, obesity
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 25.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Computerised tomogram head
Electroencephalogram
Feeling cold
Impaired work ability
Magnetic resonance imaging
Nausea
Pallor
Postictal state
Respiratory arrest
Scan with contrast
Seizure
Tongue biting
Vomiting
Symptomtext
Patient complained of feeling cold, nauseated when getting up in the morning and stated that he had felt cold all night long and could not get warm. Appearance was pale. Dressed in multiple layers of clothing. Rode with me in the car as to not leave him alone. While sitting in the car he became more nauseated and vomited. When he leaned back onto the car seat he began to seize biting his tongue and then stopped breathing. Pulse was present. 911 called. Breathing gradually returned. EMS took him to the hospital where he remained for 4-6 hours. He was released from the hospital after the post distal stage passed and he could function. He was so weak that he did not return to work for 10 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory arrest
- Hospital-Tage
- -
- Labordaten
- Laboratory test CT of the Head Follow up with Neurologist Additional tests MRI with and without contrast /. And EEG. /. Increase in Seizure medication to 300 mg bid Follow up with Primary Care Physician
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Epilepsy
- Andere Medikamente
- Lamictal 250 mg bid Atorvastatin 40 mg daily MVI
- Allergien
- No Known food allergies Environmental - caterpillars
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Brain operation
Cerebral haemorrhage
Haemorrhagic stroke
Symptomtext
Report of patient hemorragic stroke with brain bleed, patient is reportedly in surgery at the moment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebral haemorrhage
- Hospital-Tage
- 2,0
- Labordaten
- unknown
- Aktuelle Erkrankungen
- NONE REPORTED
- Vorgeschichte
- BLOOD PRESSURE, ACID REFLUX
- Andere Medikamente
- NONE REPORTED
- Allergien
- NONE REPORTED
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bone pain
Chills
Fear of death
Feeling abnormal
Insomnia
Pain
Pain in extremity
Vaccination site erythema
Vaccination site infection
Vaccination site pain
Symptomtext
Potential infection at injection site; More pain at injection site; Redness around the injection area that is about 4.5 inches long and 4.5 inches wide/ The redness appears to be spreading too; Chills and shivering; Felt strange; Arm felt like hammer; Unable to sleep at night; Pain like getting stabbed with pins was really bad; Aches and pain in her bones; she's scared to death; This spontaneous case was reported by a consumer and describes the occurrence of INSOMNIA (Unable to sleep at night), PAIN (Pain like getting stabbed with pins was really bad), BONE PAIN (Aches and pain in her bones), VACCINATION SITE INFECTION (Potential infection at injection site) and FEAR OF DEATH (she's scared to death) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Previously administered products included for COVID-19 vaccination: Johnson & Johnson (First dose (Primary series)) on 10-Jul-2021. Past adverse reactions to the above products included No adverse event with Johnson & Johnson. On 24-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In January 2022, the patient experienced FEAR OF DEATH (she's scared to death). On 25-Jan-2022, the patient experienced INSOMNIA (Unable to sleep at night), PAIN (Pain like getting stabbed with pins was really bad), BONE PAIN (Aches and pain in her bones), FEELING ABNORMAL (Felt strange), PAIN IN EXTREMITY (Arm felt like hammer) and CHILLS (Chills and shivering). On 26-Jan-2022, the patient experienced VACCINATION SITE INFECTION (Potential infection at injection site), VACCINATION SITE PAIN (More pain at injection site) and VACCINATION SITE ERYTHEMA (Redness around the injection area that is about 4.5 inches long and 4.5 inches wide/ The redness appears to be spreading too). At the time of the report, INSOMNIA (Unable to sleep at night), PAIN (Pain like getting stabbed with pins was really bad), BONE PAIN (Aches and pain in her bones), VACCINATION SITE INFECTION (Potential infection at injection site), FEAR OF DEATH (she's scared to death), FEELING ABNORMAL (Felt strange), PAIN IN EXTREMITY (Arm felt like hammer), VACCINATION SITE PAIN (More pain at injection site), VACCINATION SITE ERYTHEMA (Redness around the injection area that is about 4.5 inches long and 4.5 inches wide/ The redness appears to be spreading too) and CHILLS (Chills and shivering) outcome was unknown. No concomitant and treatment medications were reported. Patient put a large bandaid around the redness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fear of death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Pulmonary embolism
SARS-CoV-2 test positive
Symptomtext
hospitalization, pulmonary emboli
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- 1,0
- Labordaten
- COVID-19 positive test result 1/18/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, COPD
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 23.06.2022
- Impfdatum
- 17.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- SC / AR
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Amnesia
Blood testosterone decreased
Central nervous system lesion
Confusional state
Endocrine disorder
Intensive care
Lethargy
Lumbar puncture
Magnetic resonance imaging head abnormal
Nausea
Noninfective encephalitis
Ultrasound scan
Symptomtext
Began as slight nausea and progressed to lethargy and memory loss followed by symptoms related to endocrine system, e.g., drastic drop in testosterone determined by primary care physician. Symptoms progressed within days to drastic memory loss and confusion and within approximately three to four weeks to mri diagnosing inflammation of the brain presenting as 3 lesions positioned in center of brain positioned directly on hypothalamus. Initial diagnosis as potential lymphoma or neurosarcoidosis to completely "rare" as described hematologist/oncologist, Dr., and eventually neuro oncologist, Dr., Hospital. Hospitalization on April 27, 2022 into Hospital Neuro Critical Care with complete shutdown of endocrine system stemming from brain inflammation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- 18,0
- Labordaten
- MRI's, ultrasounds, 4 lumbar punctures. Dates ranging from February 2022-April 17, 2022.
- Aktuelle Erkrankungen
- December, 2021 diagnosed with Covid-19
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Lasinipril (high blood pressure med) Supplements: Multivitamin, Vitamin D,
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 33,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Amnesia
Chest pain
Computerised tomogram
Dysphemia
Electrocardiogram
Electroencephalogram
Gait disturbance
Heart rate decreased
Hypotension
Laboratory test
Loss of personal independence in daily activities
Magnetic resonance imaging
Muscle spasms
Repetitive speech
Speech disorder
Syncope
X-ray
Symptomtext
After 1st vaccine-hypotension, low heart rate, generalized fatigue, muscle aches and spasms After 2nd vaccine-increased hypotension, low heart rate, syncopal episodes, severe muscle spasms, stuttering, short term memory loss, unable to ambulate without assistance, unable to complete ADLs without assistance., chest pain, unable to speak correctly, repeative speech
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 26,0
- Labordaten
- MRI. CT scans, lab work, eegs, xrays, ekgs
- Aktuelle Erkrankungen
- Covid 19 positive Jan 18, 2022
- Vorgeschichte
- fibromyalgia bipolar I with PTSD hypothyroidism menapause-complete hysterectomy 8/2016 narcolepsy
- Andere Medikamente
- Levothyroxine 0.125mcg daily Thiamine 100mg daily Bariatric multivitamin daily gabapentin 400mg three times a day xanax 1mg twice a day prn trintellex 10mg daily imitrex prn collagen tab daily estradiol 1mg daily Nuvigil 200mg daily
- Allergien
- trileptal, phenergan, demerol, stadol, toradol, tamiflu
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 01.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anticoagulant therapy
Computerised tomogram thorax abnormal
Condition aggravated
Hypertension
Imaging procedure
Oxygen saturation decreased
Pulmonary thrombosis
Respiratory rate increased
Syncope
Symptomtext
A week after vaccination, patient was leaving a restaurant with family, she raced kids to the car where she collapsed. Emergency was called, BP was high respiration rate was high but O2 was low. Patient's vitals recovered after rest, she went home then symptoms came back when she went up the 7 stairs to get in her house, she called the squad and was taken to the ER at hospital. ER took vitals then did a CT that showed a blood clot in her right lung. ER started medication in IV and patient was admitted due to size of clot. She was airlifted to another hospital . More images were taken at hospital to determine if DVT was present. Patient was at hospital until 02/11/2022. Patient is currently on Eliquis 5mg every 12 hours until August and will follow-up with Dr. and pulmonology at the hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary thrombosis
- Hospital-Tage
- 3,0
- Labordaten
- CT scan in ER and multiple imaging studies at hospital
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure; high cholesterol
- Andere Medikamente
- hctz 12.5mg po qam; life multivitamins 1 po qam; hair, skin and nails 2 gummies po qam; flaxseed cap 1 po qam; fish oil 500?mg 1 po qam ;
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Symptomtext
Description of Event Pt received vaccination at 1205. Experienced dizziness with syncopal episode at 1224. Interventions:Patient given water, instructed to lie recumbent, vital signs taken, observed for 30 mins. Medications administered: none Response to interventions and/or medications given: Patient status improved. Disposition:Home Treatment Pt accompanied by mother.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anaphylactic reaction
Interchange of vaccine products
Pharyngeal swelling
Pruritus
Swollen tongue
Symptomtext
Anaphylactic allergic reaction to the shot. Pt began with itching. Was given 25 mg liquid Benadryl, symptoms progressed to tongue swelling, then throat swelling, Epipen given and EMS called to the facility. Pt was treated with steroids' and a second Epipen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- Blood pressure and Pulse OX measurements were taken , not sure what other tests were performed at the hospital or by EMS
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- High Blood Pressure, High cholesterol
- Andere Medikamente
- None
- Allergien
- Allergies to sudafed, doxycycline, moxifloxacin, azithromycin - has some food allergies also
- Vorherige Impfungen
- covid vaccine - janssen - mild itching, rash in mouth
- Staat
- KS
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood glucose normal
Fall
Syncope
Symptomtext
Patient fainted and fell out of chair within 5 minutes of receiving vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- blood pressure (normal ) blood sugar (normal)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Loss of consciousness
Syncope
Symptomtext
Patient received COVID booster and fainted about 1 minute afterward while still sitting in the chair when pharmacist was cleaning arm and applying bandaid. Patient did announce he was feeling light headed to warn pharmacist before losing consciousness. Pharmacist called for help from the pharmacy and then patient was assisted to the floor to lay down when he regained consciousness during the process. Patient was given a jacket to rest his head on, an ice pack to place on his forehead and a bottle of water to drink. He remained laying down for 5 minutes, then tried sitting up but still felt lightheaded so laid back down. It took patient about 20 minutes to feel better and be able to get up and walk to a chair in front of the pharmacy for further observation. Patient sat in front of pharmacy for 10 more minutes and then left on his own after feeling better. He did not have any injuries and EMS was not contacted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- bipolar disorder
- Andere Medikamente
- Divalproex ER 500mg
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Lacrimation increased
Symptomtext
Bell's Palsy - left eye began watering on Thursday, left side of mouth does not move when I smile, went to doctor on Friday (today) and he diagnosed me with Bell's Palsy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- diabetes, HPB
- Andere Medikamente
- metformin, Synthroid, Zoloft, amlodipine, verapamil, fosinopril, Jardiance
- Allergien
- penicillin, Reglan, latex
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Amnesia
Dizziness
Electrocardiogram normal
Fall
Fatigue
Bradycardia
Flushing
Hyperhidrosis
Hyporesponsive to stimuli
Hypotension
Depressed level of consciousness
Dyskinesia
Nausea
Posture abnormal
Gait disturbance
Head injury
Headache
Illness
Symptomtext
Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Medium, Systemic: Hypotension-Medium, Additional Details: This NP was called to pharmacy waiting area after a pt reportedly passed out after a vaccine. Upon arrival at PT's side BP was 102/52 with a pulse of 52, Pt was alert but minimally verbal and would not clearly answer questions, EMS activated. No cervical tenderness noted, no seizure-like activity present, unsure of head strike. Pt was diaphoretic and lying supine, BP 2 min after arrival was 92/60 with a HR of 68. PT was intermittently bradycardic. Transported to Hospital by EMS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 16.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Seizure
Symptomtext
pt had a seizure around 15 minutes after vaccination while waiting in observation area
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- seizure disorder
- Andere Medikamente
- divalproex, levetiracetam
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Pain
Pain in extremity
Symptomtext
patient received vaccine, was fine sitting in chair, stated she moved her arm and felt pain and passed out
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none noted
- Vorgeschichte
- none noted
- Andere Medikamente
- none noted
- Allergien
- nkda
- Vorherige Impfungen
- patient stated she had previously had this issue with other vaccines
- Staat
- PA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 07.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Blood glucose normal
Dizziness
Face injury
Loss of consciousness
Nausea
Syncope
Symptomtext
PATIENT WAS SITTING AT STATION AND PASSED OUT AND BANGED LEFT SIDE OF FACE AND FAINTED ON TO THE FLOOR. 911 WAS CALLED, PATIENT ASKED "WHERE AM I?" AND COULD NOT RECOGNIZE MOM. AFTER ABOUT 30 SECONDS PATIENT RECOGNIZED MOM AND THEN SAID SHE REMEMBERED FEELING LIGHTHEADED BUT NOTHING ELSE FROM THE INCIDENT. EMS TOOK BLOOD PRESSURE AND GLUCOSE READING WHICH WERE NORMAL BUT THE PATIENT FELT NAUSEA SO SHE WAS PUT ON STRETCHER AND
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- NORMAL BLOOD PRESSURE AND GLUCOSE READING
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- GLUTEN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 08.08.2023
- Impfdatum
- 28.01.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 26,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Hypotension
Symptom recurrence
Symptomtext
HYPOTENSION 3/11/2022, 8/21/2022, 11/21/2022, 11/29/2022, 3/14/2023, 2/4/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 19.04.2023
- Impfdatum
- 15.04.2022
- Beginn
- 14.09.2022
- Tage bis Beginn
- 152,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
COVID-19
Cough
Migraine
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
9/14/22 I had a bad sore throat, low in the neck. It lasted for four hours, then disappeared. I began coughing. Then I got a migraine for four hours, then it went away. My sense of taste and smell were gone. I took an at home COVID test that was positive. I emailed my doctor?s office and the doctor said I did not need an anti-viral for this type of COVID. The cough was horrible, and I could not stop coughing. In January the doctor prescribed a cough medication, pills, and warm honey that did not work. I continue to have the cough, but it is better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- 14SEPT23-At Home COVID Test-Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Vitamin E, Hydrochlorothiazide, Multi Vitamin, Bio Complete Probiotic
- Allergien
- Penicillin, Sulfa Drugs
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 29.01.2023
- Impfdatum
- 30.03.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 63,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Acoustic stimulation tests abnormal
Condition aggravated
Deafness unilateral
Electronystagmogram
Impaired work ability
Meniere's disease
Speech disorder
Tinnitus
Vertigo
Symptomtext
Approximately 3 months after receiving the booster Covid vaccine, I developed an echo in my left ear resulting in significantly reduced speech discernment. I also had a significant increase in meneires vertigo attacks resulting in missed work. As of December 16th, 2022 I am completely deaf in my right ear.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Hearing test- 09/06/2022, 10/07/2022, 01/13/2023 VNG- 10/12/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Meneires disease
- Andere Medikamente
- Yes
- Allergien
- Sulpha drugs, augmentum
- Vorherige Impfungen
- Jansen Covid vaccine 03/12/2021, age 51
- Staat
- NJ
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 20.01.2023
- Impfdatum
- 24.01.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 12,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Asthma
Dyspnoea
Histamine level increased
Parosmia
Pruritus
Rash
Symptomtext
My immune system went into overdrive and produced an overwhelming amount of histamines. I had a rash for weeks, developed asthma, itched on my scalp and other parts of my body. Developed severe anxiety. Developed ghost smells of things that were not present in my environment. I was prescribed some OTC and prescription strength medications including: METHYLPREDNISOLONE 4 MG DOSEPK, LEVALBUTEROL TAR HFA 45MCG INH HFA AEROSOL INHALER, WIXELA 100-50 INHUB BLISTER WITH DEVICE, MONTELUKAST SOD 10 MG TABLET, QVAR REDIHALER 80 MCG HFA AEROSOL BREATH ACTIVATED, SYMBICORT 160-4.5 MCG INHALER HFA AEROSOL INHALER, Pepcid AC and Benadryl. My severe symptoms lasted for more than 90 days and I still suffer from time to time with itching all over my body and some difficulty breathing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Had Omnicron from 12/26/21 to 12/31/21
- Vorgeschichte
- Borderline high blood pressure and cholesterol
- Andere Medikamente
- Atorvastatin, Lisinopril, Multivitamin
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 13.10.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Blood test
Cough
Dysphonia
Dyspnoea
Gait disturbance
Limb injury
Oropharyngeal pain
Pain
Pulmonary congestion
Pulmonary function test
Rheumatoid factor
SARS-CoV-2 test negative
Sleep study
Sputum discoloured
Vocal cord paresis
X-ray
Symptomtext
Frequent severe coughing attacks, at one point I damaged my shoulders and experienced excruciating pain walking between May and June Difficulty breathing. I have shortness of breath, overproduction of thick green phlegm, change in voice (likely some form of vocal paresis), regular severe pain in throat, and regular lung congestion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- April 15th, Negative Covid-19 Test at Private Provider April 19th, 2022, Went to Hospital Over Difficulty Breathing, Medical Examination plus X-Rays at local Hospital. May 4th, 2022, General Blood Test May 31st, 2022, X-rays at Imaging center. June 2nd, 2022, Sleep Lab Done at local Sleep Clinic. June 5th, Negative Covid-19 Test at Private Provider August 17th, 2022, Lung Breathing Exam in Doctor Office September 1st, 2022, Rheumatology Panel
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Mild allergies to dust, pollen and certain nuts.
- Andere Medikamente
- None.
- Allergien
- Mild allergies to dust, pollen and certain nuts.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 56,0
- Geschlecht
- M
- Eingang
- 18.08.2022
- Impfdatum
- 07.04.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 24,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Hypertension
Symptomtext
Hypertension has risen since last booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hypertension
- Vorgeschichte
- Hypertension
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 17.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Atrial fibrillation
Blood potassium decreased
Blood test abnormal
Chest X-ray normal
Dyspnoea exertional
Echocardiogram normal
Electrocardiogram abnormal
Extra dose administered
Fatigue
Feeling cold
Feeling jittery
Heart rate increased
Mobility decreased
Nasopharyngitis
Pain
Pyrexia
SARS-CoV-2 test negative
Symptomtext
On the morning of April 21, 2022, around 9-10 AM, I felt very jittery like I had too much caffeine. At some point in the morning, I put on my pulse oximeter and checked my oxygen saturation and heart rate. My rate was between 113-140. Every time I checked it would be slightly different. My oxygen was in the normal range between 94-96. I thought that was very odd that my heart rate was that fast. I didn't have any other symptoms other than feeling jittery, feeling fatigued, and having a rapid heart rate. I called my doctor's office to see if I could be seen and they didn't have an appointment for that day. I told them I needed to be seen sooner and they said to go to the urgent care facility. It was around 3pm when I went over there and a nurse practitioner examined me and did an EKG. When he returned, he noted that I was in afib and he recommended to go to the ER at the near by hospital. It was a little alarming to me because he said I shouldn't go home and I needed someone to take me there. My husband came back and picked me up and drove me to the emergency room at Medicine Hospital. We walked in and I had a print out from the urgent care that had determined I was in afib. They told me it was going to be a long wait. I got into a room within 5 minutes, had an IV and another EKG, Chest x-ray, and COVID swab. I saw the emergency doctor and there was discussion about being in afib and they noted it would be better to be seen by a cardiologist. I was there for about 5 hours. 5pm-10pm. they determined that I was handling my heart rate well and started me on a blood thinner Eliquis 5mg twice daily. They started me on a beta blocker Metoprolol 25mg twice daily. They also did give me some potassium as well because the potassium was low on my blood work. They administered those to me in the hospital and watched me. When they got my heart rate down to 100 and lower, and testing to see if I was actively having a heart attack. They determined I didn't have one and I wasn't having one. About 10pm, my husband came back and got me. They gave me a referral to see a cardiologist and told me to take the Eliquis and metoprolol at home. They told me to make an appointment with the cardiologist in their department. My heart rate managed to stay around 100 or lower. The next day I called their cardiology department and made the appointment for April 28. At that appointment, we did another EKG and I was still in afib and talked about my treatment. They recommended an echocardiogram which I did on May 13, 2022. I am scheduled to have a cardioversion on June 10, 2022. She talked about what the cardioversion would do and what other options there were if the cardioversion did not work. I do have an appointment for July 29 with another cardiologist for a procedure called an ablation if the cardioversion does not work. I've continued to take the blood thinner and beta blocker twice daily. My symptoms are that I get short of breath if I exert myself exercise, climbing stairs, etc. I have to stop and I'm just tired all the time. My cardiologist said that the symptoms of the beta blocker is fatigue. So between the afib and the treatment, I can't tell which is making me tired. But I'm just tired. I'm active with walking 3 times a week, gardening ? all of that stuff has been left to the side for the mean time. On top of this, just recently caught a cold on May 21.The day I got the 4th vaccine, I didn't have any reaction that day. But the next day, I was in bed all day. Chills, fever aches. The 19th those effects were gone I was still fatigued. 20th I was fatigued. 21st I was still fatigued as well and that's when I decided to put on the pulse oximeter. I could have gone into afib earlier, but I wasn't sure. The doctor told me that the echocardiogram could tell if there was any heart damage, but luckily there has been no damage.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- 04/21/2022 - EKG Urgent Care - Afib, 04/21/2022 - EKG ER - Afib, 04/21/2022 - Chest X-ray ER - nothing indicated, 04/21/2022 - COVID Test ER - negative, 05/13/2022 - Echocardiogram - Cardiologist - Heart function normal, no damage indicated from afib
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hx of skin cancers ? Basal cell carcinomas, Hx of kidney stones
- Andere Medikamente
- Hydrochlorothiazide 12.5mg daily, Vitamin D3 1000mg daily, Vitamin B12 25,000mcg daily, Premarin 0.625mg twice weekly, Possibly Aleve as needed
- Allergien
- Erythromycin - hives
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 20.01.2022
- Beginn
- 15.05.2022
- Tage bis Beginn
- 115,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
Influenza A virus test positive
Influenza B virus test positive
Oropharyngeal pain
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID infection. Sore throat and some SOB
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Positive SARS-CoV-2 (COVID-19) and Influenza AB by Nucleic Acid Amplification on 5/15/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Morbid obesity, chronic kidney disease, congestive heart failure, anemia of chronic disease, hyperkalemia, end stage renal disease, hyperlipidemia
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 16.03.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram head normal
Confusional state
Dysarthria
Pyrexia
Tremor
Symptomtext
Confusion, slurred speech, fever, both hands with tremor
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Pt left ER AMA on the day she developed symptoms. CT head done as outpatient 3/29/2022 was normal
- Aktuelle Erkrankungen
- had appointments for chronic pain from lumbar spinal stenosis. bilat carpal tunnel syndrome approximately within 1mo prior
- Vorgeschichte
- chronic pain from lumbar stenosis, osteoarthritis. bilat carpal tunnel syndrome, hypertension, gallstones, osteoporosis, chronic anemia, peripheral edema, hx poliomyelitis, hx gastritis, hx anemia, vitamin D deficiency
- Andere Medikamente
- Morphine, Oxycodone, Gabapentin, Albuterol, Hyzaar, Magesium- Oxide, Alendronate, MVI, Tylenol
- Allergien
- Cymbalta (rash)
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 16.03.2022
- Beginn
- 25.04.2022
- Tage bis Beginn
- 40,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
COVID-19
Dyspnoea
Fatigue
Headache
Malaise
Oropharyngeal pain
Pain in extremity
Productive cough
SARS-CoV-2 test positive
Sinus pain
Sputum discoloured
Symptomtext
AE- sore arm for 36 hours and a headache for about 2 days. I did not have fever. 04/25/2022 - I started feeling sick, sore throat, then I had a barking sort of cough, but it was productive, originally was clear and then started getting yellowish-tint. Loss of sense of smell. Pain in my left maxillary sinus and frontal sinus. The symptoms prompted me to take a COVID-19. I took a home test, one in the morning BinaxNow was negative. I did Flo fax at home that night- negative. I took the PCR test-04/27/2022, I got the results, 04/28/2022- it was positive. I talked to the nurse, given my diagnosis, I was given Paxlovid- 4/28/2022, I started it on late afternoon. I am not totally better, but I am feeling better than 2 days. I have noticed overwhelming tiredness. I have been sleeping for like 10 hours and I never sleep for 10 hours. Unknown because I noticed I was feeling better one night and I was feeling worse when I woke up. I have also noticed I am more short of breath than I usually am. I am getting better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- PCR COVID-19 Test 04/27/2022 - results 04/28/2022 -positive
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- lung cancer- I never smoked - diagnosed 04/2018, asthma, 6 sinus surgeries in hospitals and a lot of minor procedures over the years, history of sinus infections, hyperactive gall bladder - bladder surgery 02/2021
- Andere Medikamente
- Levo albuterol inhaler, Singulair, Allegra, Memantine, Sunosi, Warfarin, Crestor, Alprazolam, Bupropion, Dexilant, Co-Q-10, Folgard, Preservision vitamins, vitamin B-2, Vitamin D-3, grape seed extract, Pepcid, L-arginine
- Allergien
- nutmeg - anaphylactic reaction, opioids - I throw up within seconds
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 22.12.2021
- Beginn
- 27.01.2022
- Tage bis Beginn
- 36,0
- Dosis
- 2
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Colitis ulcerative
Colonoscopy abnormal
Condition aggravated
Diarrhoea
Diarrhoea haemorrhagic
Symptomtext
Diarrhea starting 1/6/2022 that hasn't stopped. Got substantially worse after 2nd dose with blood and mucus. Diagnosed as Ulcerative Colitis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Colonoscopy at facility.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Zyrtec
- Allergien
- Celebrex
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 12.04.2022
- Impfdatum
- 28.07.2021
- Beginn
- 10.04.2022
- Tage bis Beginn
- 256,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Chest X-ray normal
Chest pain
Dizziness
Dyspnoea
Productive cough
Pyrexia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Wheezing
Symptomtext
Covid19 breakthrough. 1st vaccine received on 07/06/2021. 66 y/o female with PMHX of ESRD on hemodialysis MWF, Asthma, CAD s/p PCI 2017, HTN, gastritis, DM, Hypothyroidism, scolosis presents to ED with c/o SOB, wheezing, productive cough, dizziness and chest pain x1 day. Room air sat 97%, CXR with no focal consolidation and pt with low grade temps. Treated with IV steroids. Covid severity score=0 per Admitting MD.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- SARS CoV 2 PCR Covid19- Detected on 04/10/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ESRD on Hemodialysis MWF, Asthma, CAD s/p PCI 2017, HTN, Gastritis, DM, Hypothyroid, scolosis
- Andere Medikamente
- -
- Allergien
- Azithromycin, Dust
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 03.03.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 29,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Differential white blood cell count
Full blood count
Laboratory test
Mobility decreased
Muscular weakness
Red blood cell sedimentation rate
Urine analysis
Symptomtext
Patient was on her knees accessing a drawer last night and then she acutely could not get up and felt profound weakness to her feet and legs. She had to "scooch" herself across the room which took a couple of hours. She denied any loss of bladder or bowel control. She basically lost her motor strength to her legs but she reports she could feel sensation to her legs. She denied any vision or swallowing problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- CBC and Dif on 04/2/22 ESR, Westergreen on 04/2/22 Routine Chemistry on 04/2/22 Cardiac markers on 04/2/22 UA macroscopic on 04/2/22
- Aktuelle Erkrankungen
- Pt. report having a head cold 3 weeks ago.
- Vorgeschichte
- Past medical history: HTN Sciatica HLD Hypothyroid
- Andere Medikamente
- carvedilol 6.25 mg PO BID clonidine 0.1 mg PO QID Duloxetine 60 mg PO HS gabapentin 300 mg PO TID hydralazine 25 mg 2.5 tabs PO BID lisinopril 40 mg (2 tabs) PO Daily nystatin topical 1 app TID Levothyroxine 112 mcg PO qday Atorvastatin 40
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 22.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Chills
Discomfort
Headache
Hyperhidrosis
Injection site pain
Lethargy
Limb discomfort
Muscle spasms
Oedema peripheral
Pain
Pain in extremity
Paraesthesia
Pyrexia
Symptomtext
After the shot I experienced severe pain in my arm where the shot was administered which did not cease for 5 days after and felt like it slowly spread into the rest of my arm which lessened but felt uncomfortable for more than 5 days. It felt like my left arm was experiencing muscle spasms and aches from my shoulder down to my pinky. During the night around 8 p.m. I also began to feel the symptoms that were said to be normal after a COVID-19 vaccination such as fever, chills, lethargy, headaches, sweats, and body aches. What I didn't expect and what alerted me the most was what I began to feel at about 6:30 am on the following morning which was the inflammation under my armpits, I'm aware that my lymphatic sacs are located there. They swelled up until I was unable to put my arms to my sides and the discomfort was unbearable, I researched and called walk in clinics for help but I currently do not have insurance and I've been waiting to be approved for health care program. Simultaneously, I started to fill a sharp pain and tingling sensation in my chest around the area where my heart is. I felt a heavy pressure on my chest for several days and the swelling under my arms did not start to lessen for 5 straight days. I'm still feeling some discomfort and slight swelling under my arms and it has now been over a week since I was vaccinated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None because I have no coverage or income to pay for a walk-in clinic.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- Impfdatum
- 24.01.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 28,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Discomfort
Heart rate increased
Hypertension
Symptomtext
Late Jan started getting a crushing feeling and fast feeling heart rate. Ignored. In March, I had a health check up for my health insurance and my blood pressure was 170/110. I went to my doctor to confirm and I was 180/120 there. I have NEVER had high blood pressure before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- 3/10/2022 tests at doctor and full blood panel done to see if it was anything else.
- Aktuelle Erkrankungen
- Cold in early January, was not covid. Family members did have covid the week of the vaccination.
- Vorgeschichte
- None
- Andere Medikamente
- Zoloft, vitamin D, Allegra, multi vitamin, milk thistle
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 05.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiomegaly
Chest discomfort
Dyspnoea
Goitre
Lung disorder
SARS-CoV-2 test negative
Splenomegaly
Vaccination site reaction
Symptomtext
First COVID arm then started devolving tightness in chest and shortness of breath. Took CT scan went to the hospital 2/24 was told I had enlarged heart ground glass opacity of left lung. Left side of thyroid is enlarged. Spleen is enlarged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- PCR- Negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Cardicemer, Hydrochlorothiazide, Lipitor, Xanax, Nexium Zyrtec
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- U
- Eingang
- 26.02.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Hypoaesthesia
Lip swelling
Swelling
Swelling face
Symptomtext
Wife came in yesterday and said that her husband got the moderna booster at around 12pm and he started to have symptoms at 9pm that same day. He had swelling of the chin, face, lips and neck, sob, diff breathing, and numbness started from the right face to the left face. She took him to the urgent care and now he is all better and back to normal. Apologized to the wife that happened to her husband but she was fine she just wanted to let us know. She also said he got 2 moderna vaccines and he was fine just the 3rd dose he got really bad reactions. put in database and vaers
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Chest X-ray
Computerised tomogram
Full blood count
Gait disturbance
Laboratory test
Magnetic resonance imaging
Metabolic function test
Speech disorder
Tremor
Symptomtext
Tremors Speech abnormality Gait disturbance Weakness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- 4,0
- Labordaten
- Mri C-X-ray Ct scan BMP CBC Drug withdrawal panel 2/10
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression
- Andere Medikamente
- Zoloft 100 Trazadone 100
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Erythema
Fatigue
Injected limb mobility decreased
Pain
Pain in extremity
Peripheral swelling
Tenderness
Symptomtext
Vaccine given on the afternoon of February 23, 2022 via intramuscular route in right deltoid. Waited 15 minutes with no immediate reaction or soreness. Arm soreness developed later that evening. On February 24, 2022, right arm became red and increasingly sore. Co-workers were able to visibly notice the area. That evening (24 hours after vaccine received), her arm became extremely sore, as well as experiencing body aches, chills and fatigue. The injection site arm became raised at this time. She was unable to lift arm above shoulder height without extreme pain. Took Tylenol Cold & Flu to help with aches and chills. On the morning of February 25, 2022, she can lift her arm somewhat better but is still very sore. She took four Advil 200 mg (800 mg total) and it helped some. Presently, arm is still very tender, sore, red, and raised. Area feels almost like a knot in the muscle.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- None at this time
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Impaired work ability
Injection site warmth
Mobility decreased
Oedema peripheral
Peripheral swelling
Tenderness
Symptomtext
On Friday my left arm was swollen twice the normal size. Then on Saturday morning started around my left arm pit on left arm was swollen (described as small orange). The injection site was hot and had fever of 100.2. I stayed in bed all day Saturday and most of day on Sunday. My joint was aching and left arm was sore to touch. On Monday I stayed home from work due to the swelling contacted my doctor. I went to see my doctor on Tuesday he stated might was a draining from my lymph node advised me to take Aleve and apply cold compress. The swelling has gone down to normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- Shrimp, NatLax
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 15.02.2022
- Impfdatum
- 08.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Palpitations
Symptomtext
Strong heart palpitations, increased blood pressure despite taking medications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Enalapril 10mg, Pepcid 20mg, Simvastatin 40 mg.
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 13.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 15,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Costochondritis
Echocardiogram normal
Electrocardiogram normal
Laboratory test normal
Oesophagitis
Polyarthritis
Troponin normal
Symptomtext
Polyarthritis without swelling/warmth/edema, chest pain worse with swallowing and movement (esophagitis, costochondritis?) Given NSAIDS, checked labs, EKG, troponin, all negative and reassuring. Echo of heart showed normal wall motion, no effusion. EKG normal. Discharged home with NSAIDS and pepcid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- See above
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest discomfort
Dizziness
Dyspnoea
Erythema
Hyperhidrosis
Interchange of vaccine products
Throat irritation
Symptomtext
Provider was called to the Vaccine Clinic for possible reaction to find patient with mild labored breathing, diaphoretic and redness to bilateral upper extremities and chest. Patient began feeling SOB, chest tightness, and dizziness reported ~10 minutes following vaccine administration. O2 sat 100% RA, pulse upper 90s to low 100s, BP 120/82. After a few minutes, symptoms unchanged and patient reporting scratchiness to throat starting. Benadryl 50mg given PO, EMS called given worsening SX of SOB and new throat concerns. Patient received J&J x1 Oct 2021, no prior Moderna vaccine before today. Patient denied prior known allergic reactions to vaccines. Paramedics transported patient to ER for further evaluation/monitoring.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None done.
- Aktuelle Erkrankungen
- Was being treated for possibly asthma/pneumonia via telephone appt.
- Vorgeschichte
- -
- Andere Medikamente
- albuterol inhaler, loratadine,
- Allergien
- lidocaine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Chills
Fatigue
Insomnia
Menstruation delayed
Muscular weakness
Neuralgia
Urinary tract infection
Symptomtext
Late menses, insomnia, UTI, chronic fatigue, body chills, muscle weakness, chest pain, extreme fatigue and nerve pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Shingles, narcolepsy, insomnia and chronic fatigue, frequent UTIs from Moderna #2 vaccine
- Vorgeschichte
- Chronic Epstein Barr, chronic Lyme disease
- Andere Medikamente
- Vyvanse 30mg
- Allergien
- -
- Vorherige Impfungen
- Shingles; narcolepsy; insomnia; UTI; BV; age 30; April 2021; Moderna vaccine #2.
- Staat
- OK
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angina pectoris
Anxiety
Blood test
Chest X-ray
Chest pain
Dyspnoea
Electrocardiogram
Gait disturbance
Hypoaesthesia
Metabolic function test
Migraine
Pain in extremity
Pyrexia
Symptomtext
Extremy left arm pain after Injection. Fever(lowgrade), migrane(extreme), heart and chest pain(went to er) difficulty breathing, numbness in lower right leg, difficulty waking, extreme anxiety/feeling of impending doom.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 2/3/22 ecg. Complete metabolic panel blood test. Chest x-ray.
- Aktuelle Erkrankungen
- Streptococcus Jan 17th 2022
- Vorgeschichte
- Hypertension
- Andere Medikamente
- None
- Allergien
- Sulfa allergy
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Paraesthesia
Symptomtext
Pt states they have tingles going down their arm. It happened right away pt states.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Body temperature increased
Chills
Dyspnoea exertional
Fatigue
Headache
Hyperhidrosis
Impaired work ability
Injection site haemorrhage
Injection site rash
Injection site warmth
Malaise
Musculoskeletal stiffness
Pain
Pain in extremity
Pruritus
Pyrexia
Rash
Symptomtext
1/6/22 8:30 pm- received booster at drug store, bled a lot. 1/7/22 7 am- sore arm; 10 am- slight headache; 12:30 pm- took Tylenol; 3:30 pm- tired leaving work; 4:30 pm- not feeling well with chills; 6:15 pm- temperature rose to 101.2 with body aches, took Tylenol; 11:45 pm- temperature 101.8 1/8/22 7 am- temperature at 101.3, took Tylenol; 9:30 am-fever went down, but lymph node under left arm pit was swollen, and sore to move arm; 11:30 am- joints ached, hurt to walk, headache/teeth ache; 12:45 pm- temperature was at 101.5, took Advil; 1:30 pm- temperature still at 101; 8:30 pm- fever down to 100.1 but sweating at night 1/9/22 9 am- no fever but rash on L arm from the injection area; 11:30 am- did not attend church, thought fever broke at 98.3 with no achiness but just a slight headache, harder breathing when walking; 5:00 pm- fever back with sweating, took Advil, rash went further down arm towards elbow 1/10/22 6am- rash from left arm spread to front neck area with low grade fever, rash on left arm holding heat, permitted to go into work; 7:30 am- sweating just sitting down; 12:45 pm- stiff neck, rash going to right arm area, called into family doc office; 1:45 pm- doc via phone visit instructed me to use Benadryl and if it didn?t improve/worsened then I would have to go to Urgent Care, 2pm- left work early, from doctor?s advice; 2:45 pm- took Benadryl; 7:30 pm- took another Benadryl, body itching 1/11/22 6:30 am- rash still with heat but no stiff neck; 4:30 pm- tired and resting at home, not better but not worse, VERS rep called to advise me to report concerns Continued to feel tired and have small rash on left arm near injection site for rest of the week
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension.
- Andere Medikamente
- Junel; Hydrochlorothiazide; Multi-vitamin; Cranberry supplement; Zyrtec; Fsh oil; Vitamin C and D; Zinc.
- Allergien
- -
- Vorherige Impfungen
- Moderna shot 2, less than Booster but rash was bad
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Back pain
Chest discomfort
Condition aggravated
Fatigue
Nausea
Palpitations
Symptomtext
Heaviness in my chest, racing heart, back and shoulder pain, fatigue, and nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- tested positive for Covid-19, first symptoms on 12/31/21 tested on 1/2/22 results back 1/6/22.
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Morphine
- Vorherige Impfungen
- racing heart, rash, fatigue, fever body aches.
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dyspnoea
Heart rate abnormal
Heart rate increased
Hypopnoea
Symptomtext
Severe shortness of breath lasting several hours. Chest pressure lasting several hours. Extremely rapid heartbeat lasting over 12 hours. The following days heart became very shallow and could not detect heart beat at any pulse area. Breathing also became shallow. Shortness of breath also returned off and on during following 7 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- In progress now will be receivjng echocardiogram and Holter monitor to study heart progress.
- Aktuelle Erkrankungen
- Heart valves damage
- Vorgeschichte
- Heart valves damage since 1981. Also heart attacks and ventricular fibrillation.
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tremor
Vaccine positive rechallenge
Symptomtext
Per patient, tremors occurred in left arm (just like after the first and second Moderna dose).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Anxiety, ADD, depression, insomnia
- Andere Medikamente
- Lorazepam, Citalopram, Hydroxyzine, Lithium, Propranolol, Doxazosin, Prazosin, Vyvanse
- Allergien
- Ketorolac
- Vorherige Impfungen
- Similar tremor occurred with the first and second dose of Moderna COVID-19 vaccine.
- Staat
- AK
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Paraesthesia oral
Pharyngeal paraesthesia
Swelling
Symptomtext
C/O throat and tongue feeling tingly and slightly swollen. This is the same symptoms she gets when she eats shellfish. Usually Benadryl will resolve shellfish symptoms. Alert and oriented. VSS. No outward signs of swelling. No difficulty swallowing or breathing. Prefers not to have 911 called. Explained our policy and that she can refuse transport after ambulance is here. Agrees to transport to Hospital ER by ambulance after EMTs arrive. Sent to ER at 1436 with symptoms unchanged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- Unknown. Was observed in ER and discharged home.
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- Reports that she will occasionally get similar allergic reactions to unknown sources that present with oral numbness and sense of tongue swelling. Shellfish cause this reaction every time but has so far resolved with benadryl.
- Andere Medikamente
- Unknown
- Allergien
- Reports allergy to shellfish
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Balance disorder
Chest discomfort
Chest pain
Cough
Dyspnoea
Erythema
Pharyngeal swelling
Urticaria
Wheezing
Symptomtext
Within 60 seconds of receiving the shot, I felt chest compression and pain and my throat swelled so that I had to wheeze and struggle for breath. I was able to talk, although I would cough as I spoke. My face turned very red and I had hives on my neck. The pharmacist gave me an injection of Benadryl 50 mg and the shortness of breath subsided. After about 15 minutes, I could breathe normally although my chest still felt tight. When I stood to go, I realized that I could not balance and I was at risk of falling. This felt different than low blood pressure or blacking out. I simply could not understand which way was "up." I wasn't thinking very clearly. 90 minutes after the vaccine, I felt well enough to drive home. 7 hours later, my chest still feels a bit tight and I had a little wheezing an hour ago, but it went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- OTC MEDICATIONS: Cetirizine Hydrochloride Tablets, 10 mg (generic). PRESCRIPTIONS: Spironolactone Tabs, 50 mg (generic); Mirena Intra-Uterine Device. DIETARY SUPPLEMENTS: B12 Microlozenge, 500 mcg; Vitamin C; 400 mg; Vitamin D3, 45 mcg; Zin
- Allergien
- Sensitive to acrylates (adhesives, such as in bandages), propylene glycol, and chlorhexidine.
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 10.04.2023
- Impfdatum
- 06.04.2022
- Beginn
- 14.11.2022
- Tage bis Beginn
- 222,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy test positive
Blood immunoglobulin E increased
C-reactive protein increased
Haematocrit increased
Haemoglobin increased
Histone antibody positive
Immunoglobulins normal
Rash
Red blood cell sedimentation rate normal
Thyroid function test normal
Vitamin D decreased
Symptomtext
I broke out in a rash in several different areas of my body. I had some allergy testing done at the dermatologist and was treated with cetirizine and famotidine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- 31JAN2023 Immunoglobulin Panel normal; 15DEB2022 Erythrocyte Sedimentation rate normal; 15DEC2022 CRP high; 15DEC2022 IGE high; 15DEC2022 Histone antibodies high; 15DEC2022 latex sensitivity high; 15DEC2022 vitamin D low; 15DEC202 Hematocrit high; 15DEC2022 Hemoglobin high;15DEC2022 Thyroid, small but normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Type 2 Diabetes
- Andere Medikamente
- NOVOLOG; TRESIBA; vitamin D
- Allergien
- Penicillin; codeine; MEFOXIN
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 16.02.2023
- Impfdatum
- 18.01.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 134,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Malaise
Pain in extremity
SARS-CoV-2 test positive
Symptomtext
I had a sore arm for about 24 hours after receiving the vaccine. I tested positive for COVID-19 in 06/2022. I had symptoms for about 24 hours prior to testing positive. On day five I contacted my doctor, and it was decided that I do not take Paxlovid. I didn't take anything for my symptoms and just dealt with it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- JUN2022 COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Prednisone
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 26.01.2023
- Impfdatum
- 25.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
COVID-19
Computerised tomogram normal
Fatigue
Headache
SARS-CoV-2 test positive
Symptomtext
The day after I took the vaccine, I had the worst headache I have ever had in my life and fatigue. I thought it was a reaction to the shot, even though the first shot I had. I always have a reaction to the flu shot so I thought it was just that. However, the fatigue and headaches kept coming and going. I had blood work done and nothing came of it, it showed nothing wrong. I contracted COVID in December of 2022 as well. We are now in January and I still get the headaches and fatigue. I did have a chiropractor appointment for my back and they did a CT scan of my back and neck but also found nothing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- CT scan of the neck and back with no results. Full blood panel with nothing abnormal.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- ZOLOFT; CRESTOR; multivitamin
- Allergien
- Mushrooms
- Vorherige Impfungen
- Flu vaccines give me the feeling of having the flu
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 10.10.2022
- Impfdatum
- 08.04.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 99,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
COVID-19
Cough
Exercise tolerance decreased
Fatigue
Headache
Hyperhidrosis
Nasal congestion
Pain in extremity
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I was extremely tired. I had a low-grade fever. Strangely my thighs and my hips ached; lasting 2-3 days. I had some nasal congestion WITHOUT a cough. I sort of had a come and go headache. The feeling of exhaustion lasted about 2-3 weeks. I noticed since testing positive; I can't tolerate exercise as well as I did before. I excessively sweat now and get tired a lot easier. Surprising my asthma did not trigger while being positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- at home COVID-19 rapid test; Paxlovid: stepped up my asthma treatment to Alvesco twice and day for 2weeks
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- Asthma; mild Hepatic Steatosis; HPV related dysplasia; History of heart dysrhythmia;
- Andere Medikamente
- Famotidine; Clomiphene citrate; Aspirin 81mg; Vitamin D3; Centrum; Allergy shots; Xolair (asthma injection);
- Allergien
- Erythromycin; Meloxican; Augmentin(possibly); History of latex allergy Buckwheat;
- Vorherige Impfungen
- Influenza, 1997
- Staat
- AL
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 01.09.2022
- Impfdatum
- 01.06.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Nasal congestion
SARS-CoV-2 test positive
Therapy change
Symptomtext
On 06/23/2022 in the morning I experienced nasal congestions; fatigue; and elevated body temperature of 99.06. I did a tele health on the same day with my doctor she only gave me vitamins most of them I already took before seeing my doctor. I started feeling better after 4 days. After 2 months of the vaccine I got hypertension. I went to the doctors office where she increased the dose of my hypertension medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 home test - positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Hydrochlorothiazide; COREG; multivitamins; vitamin D; zinc; vitamin C; CLARITIN
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 31.07.2022
- Impfdatum
- 17.01.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 74,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
X-ray
Symptomtext
pain in right wrist, especially when lifting anything heavy or bending the hand backwards. This began sometime in April 2022, I don't remember exactly. I listed this on the V-Safe check-in to be thorough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Visual and manual examination of my wrist, followed by X-rays. Referral to occupational therapy, treatment started July 2022.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- multiple sclerosis, arthritis, depression
- Andere Medikamente
- gabapentin, bupropion, mirtazapine, Ritalin, lisinopril, Ocrevus, naproxen, vitamin D
- Allergien
- Bactrim, cephalosporins, possibly stevia or erythritol
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 15.04.2022
- Beginn
- 25.06.2022
- Tage bis Beginn
- 71,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dysphonia
Nasal congestion
Nasopharyngitis
Oropharyngeal pain
SARS-CoV-2 test positive
Upper-airway cough syndrome
Symptomtext
On June 25, 2022 I began to have a head cold with a sore throat. I never had a fever. I did a home test on the 26th and it was negative. On June 30th since I was not getting better I went in to have a PCR and it was positive. I began taking Claritin and the inhaler prescribed and symptoms began to decrease. On July 7th I had a home test and it was negative. On July 24th I had another PCR test and it was negative. As of today, the only symptoms I have are stuffy feeling in my head and nasal drip with a slight cough. I also have a hoarse voice.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test, negative; PCR test, positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Shoulder replacements
- Andere Medikamente
- Metamucil; Osteobiflex; Lutein; Fish Oil; Cranberry; Vitamin D3; Pepto Bismol; Visviome; CoQ10; Vitamin B Complex; Baby Aspirin; Atorvastatin; Viest; ProAir SHA
- Allergien
- Penicillin; Chromium
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 25.07.2022
- Impfdatum
- 21.01.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 144,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Oropharyngeal pain
SARS-CoV-2 test positive
Sinus congestion
Sinus operation
Symptomtext
On 06/14/2022 I woke up and felt my sinus were full. I took a home test 06/17/2022 and it was positive. The next day I went to urgent care and had a PCR test that also showed positive. I had drainage, cough, sore throat and fatigue. It was too late to start any medications but I did take a steroid. As of today I am only having a lingering cough that does continue to get better and less frequent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test 06/17/2022 positive. PCR COVID-19 test 06/18/2022 positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure; High Cholesterol
- Andere Medikamente
- Sertraline; simvastatin; pantoprazole; losartan with hydrochlorothiazide
- Allergien
- Shellfish
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 04.02.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 34,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Aphonia
Blood test
Computerised tomogram
Computerised tomogram normal
Deafness
Ear infection
Ear pain
Fungal infection
Headache
Hypersensitivity
Infection
Laboratory test
Muscle tension dysphonia
Pain
Pruritus
Urinary tract infection
Symptomtext
She got her vaccine (booster), she had no reaction at first, then around 3/10/22 she started getting sick with an ear ache. She went to the UC she had an ear infection. They gave her antibiotics. Then after the ear infection she lost her hearing for 2 weeks, so she went back to the doctor and they gave her more antibiotics. The next thing she remembers is she went to the ENT and they checked her vocal cords as she had lost her voice, and they were strained. They gave her some antibiotics too. Then after that she went back to UC because she had a really bad headache that would not go away, possibly due to the infection. She went to Hospital as she was hurting so bad, and they gave her a CT scan if the infection had gone to her brain but it had not done that. They gave her more antibiotics. Her head kept hurting and she went back to UC and found out that she had a UTI, so she was put on more antibiotics. Then, she went back to the UC again and they recommended a different antibiotic and she started taking those. She finished the antibiotics and went back to the UC as she had a yeast infection and was given more antibiotics. As of today, she hasn't been back to the UC but believe the UTI is still there. Her skin is itching really really bad, so they gave her some Benadryl to take, which is not working. She has been scratching her skin up so bad because she is having the allergic reaction to the booster shot. She has been itching since 3/10/22. She kept getting back to back infections and nobody knew why and just kept getting sicker and sicker. They kept asking her what she did differently and last Friday she figured out that it was the booster shot that she had done differently, and thinks this was related to all of her infections. She feels the booster shot did not agree with her system.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear pain
- Hospital-Tage
- -
- Labordaten
- As above, CAT scan, blood work, lab work.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Diabetes, high blood pressure.
- Andere Medikamente
- Ambien 10 mg.
- Allergien
- Tetracycline.
- Vorherige Impfungen
- 7 years ago she got a flu shot and got really sick from that, and has not taken that since.
- Staat
- MD
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 14.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 02.06.2022
- Tage bis Beginn
- 55,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dysphonia
Feeling abnormal
Feeling cold
Nasopharyngitis
Oropharyngeal pain
Pain
SARS-CoV-2 test positive
Symptomtext
On 06/02/2022 I began to experience a mild throat soreness around noon. The next day I woke up and my throat felt like I had a whole bunch of little incisions all around my throat and it was really painful. Toward the middle of the day it began to feel more like a head cold. These events normally occur when I get minor illnesses so I thought it was just a cold. By Saturday, my symptoms had progressed and I was having body aches and I was feeling really cold. By the time I was going to bed that night, I felt like my symptoms were less than normal so I took an at home COVID-19 test which was very obviously positive. When I woke up on Sunday, I was still feeling badly but was feeling slightly better than the day before. Since my primary care doctor is not available on Sundays, I called a local urgent care type facility. I was informed that I could not take Paxlovid due to a medication that I am currently prescribed so they suggested that I could receive a Monoclonal Antibody infusion. On Monday, when I heard from them about the monoclonal antibody therapy, I was already feeling better to the point that I did not feel that it was needed. It took 4 or 5 more days for my throat to begin feeling normal again but at this point, all of my symptoms have subsided with the exception of some changes to my voice that may have been caused by my extremely sore throat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- At home COVID-19 test-positive-06/04/2022
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Benign Enlarged Prostate; High Cholesterol; Osteoarthritis; Sleep Apnea; Obesity.
- Andere Medikamente
- Lipitor; Finasteride; Alfuosin; Tadalafil; Zyrtec; Multivitamin; Vitamin B; Potassium; Probiotic.
- Allergien
- Walnuts; Artificial Cheese; Jello.
- Vorherige Impfungen
- Anthrax Vaccines-Extreme redness and soreness at injection site. COVID-19 vaccines-head fog.
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 14.07.2022
- Impfdatum
- 28.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chronic spontaneous urticaria
Immune system disorder
Lip swelling
Peripheral swelling
Swelling face
Urticaria
Symptomtext
I developed a Chronic Spontaneous Urticaria for the first time, a few days later of getting the booster shot, presenting swelling of my lips , facial area, hands and feet and hives all over my body. Several doses of steroids were administered as well as high doses of antihistamines for more than a week. Symptoms have been controlled by taking cetirizine 10mg daily. However, symptoms becomes severe if I stop the medication for one day. I have been seen an allergist/immunologist who concludes that based on my health history and evaluation; that my immune system was over-stimulated by the 3rd booster shot of the Moderna Covid-19 Vaccine, thus causing this chronic condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chronic spontaneous urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Covid 19 a month prior to vaccination.
- Vorgeschichte
- None
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 49,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Fatigue
Malaise
Pain
Rhinorrhoea
SARS-CoV-2 test positive
Throat irritation
Symptomtext
I contracted COVID-19 on 05/31/2022 with symptoms of scratchy throat, runny nose, body aches, and fatigue. I was not prescribed any medications for my symptoms. I was ill for 12 days before my symptoms began to resolve. I am fully recovered with no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 rapid nasal swab home test was positive on 06/02/2022.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Sleep Apnea
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 08.04.2022
- Beginn
- 28.05.2022
- Tage bis Beginn
- 50,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
COVID-19
Dizziness
Fatigue
Headache
SARS-CoV-2 test positive
Symptomtext
Although I had two initial Pfizer vaccinations, one Pfizer booster and one Moderna booster, I still caught COVID-19. I did not have a bad cough or fever, but I was dizzy, extremely fatigued, had a bad headache and developed severe lower back pain. I took Paxlovid for five days and was generally better after that, but my lower back pain has continued.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- Tested positive using home test for six days.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Olmesartan, HCTZ, Baby Aspirin
- Allergien
- Pennicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 16.04.2022
- Beginn
- 04.07.2022
- Tage bis Beginn
- 79,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Headache
Pyrexia
SARS-CoV-2 test positive
Sinus pain
Upper-airway cough syndrome
Symptomtext
Monday, July 4, I began running a fever and got up to take home COVID-19 test and it was positive. My symptoms were mostly sinus head pain and just really tired. Post nasal drip caused me to cough. I had a tickle in my throat that caused me to cough. Fever only lasted one day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home COVID-19 test, positive; PCR COVID-19, positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Ocular Melanoma
- Andere Medikamente
- OCUVITE; turmeric; multivitamin; B complex; calcium; vitamin D3
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 07.07.2022
- Impfdatum
- 06.04.2022
- Beginn
- 04.07.2022
- Tage bis Beginn
- 89,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Discomfort
Dysphonia
Fatigue
Headache
Illness
Impaired work ability
Nasal congestion
Rhinorrhoea
SARS-CoV-2 test positive
Tenderness
Throat irritation
Symptomtext
I received my second Moderna booster for COVID-19 on 4/6/2022. On the night of 7/4/2022, I developed a runny nose, a very slight headache, nasal congestion, a slightly scratchy throat, and a tenderness in both inner ears. When I woke up the morning of 7/5/2022, the symptoms were pretty much the same, though the headache was gone. I went ahead and went to work, because it just felt like I was getting a cold. As the day progressed at work, though, I noticed that my voice wasn't the same, as I sounded congested. That evening, the nasal congestion worsened. On the morning of 7/6/2022, the symptoms were pretty much the same, though slightly worse. As I was getting ready for work that day, it occurred to me that I had heard that COVID-19 symptoms are similar to those of a cold, so I took an at-home test, and the result was positive. I immediately called in sick to work and went to the urgent care clinic and underwent a PCR test. The PCR test also yielded a positive result. The NP or PA at the urgent care recommended that I treat my symptoms with OTC medicines like nasal spray and CLARITIN or ZYRTEC, which I did. She also told me to isolate at home for 5 days and told me I could leave the house afterwards as long as I wore a mask for 5 more days afterwards. On the night of 7/6/2022, I again had a slight headache, but it was nothing major. It was so mild that I didn't even take medicine for it. During my illness, I haven't felt especially bad. I'm slightly more tired than usual and aside from the discomfort caused by the abovementioned symptoms, I feel mostly fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 03.07.2022
- Impfdatum
- 25.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Vaccination site pain
Symptomtext
headache; sore arm; This spontaneous case was reported by a patient and describes the occurrence of HEADACHE (headache) and VACCINATION SITE PAIN (sore arm) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 prophylaxis. Previously administered products included for Drug use for unknown indication: JNJ (received JNJ vaccine initially). Past adverse reactions to the above products included No adverse event with JNJ. On 25-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In January 2022, the patient experienced VACCINATION SITE PAIN (sore arm). On 25-Jan-2022, the patient experienced HEADACHE (headache). The patient was treated with IBUPROFEN at an unspecified dose and frequency. In January 2022, HEADACHE (headache) and VACCINATION SITE PAIN (sore arm) had resolved. No concomitant medication was reported. Patient got the Moderna booster dose. A couple hours after administration when she came home, she experienced the headaches. Both side effects lasted about a day. This case was linked to MOD-2022-595774 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 29.06.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood pressure decreased
Blood pressure increased
Feeling hot
Pain
Pain in extremity
Pharyngeal swelling
Pyrexia
SARS-CoV-2 test negative
Symptomtext
05/2022 Within 12 hours of vaccination, I woke up in middle of night I was running a fever, felt like throat was swelling, achy, hot. Arm was sore. This continued to run fevers. I had husband take me for 2 COVID-19 tests. Blood pressure kept spiking to over 200's and then dipping real low below the 100's. I started wearing my cuff daily. Regular Dr. said to go to the ER. Adjusted some medicines at the ER. Put on prednisone, high doses. Almost for 2 1/2 weeks. My blood pressure continued being off the charts. It only recently started to go back to normal digits. The worst was 216/116. Dr and ER said to never to take the vaccinations again. It delayed me getting my breasts MRI and biopsy, delaying my health care after the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- COVID-19; negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hashimoto's disease; Breast cancer survivor; Reflux; Vertigo; Tinnitus; Micardis
- Andere Medikamente
- Vitamin D; Calcium; Magnesium; Zinc; Colace
- Allergien
- Cipro; Daypro; Suplosporone; Ace inhibitors; Statin Sensitive; Mobic; Compazine; Nickel; Latex; Codeine; Mold; Bee; Lactose and Dairy Intolerance
- Vorherige Impfungen
- COVID-19 feeling sick after for about 3-5 days after
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 30.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Eye pain
Fatigue
Headache
Inappropriate schedule of product administration
Insomnia
Myalgia
Oropharyngeal pain
Symptomtext
sore throat; eye aches; difficulty sleeping; Extreme fatigue; body aches; chills; headaches; Patient took Pfizer dose 3 on 19-Mar-2022 and Moderna dose 4 on 30-Mar-2022; This spontaneous case was reported by a patient and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient took Pfizer dose 3 on 19-Mar-2022 and Moderna dose 4 on 30-Mar-2022), OROPHARYNGEAL PAIN (sore throat), EYE PAIN (eye aches), INSOMNIA (difficulty sleeping) and FATIGUE (Extreme fatigue) in a 65-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Previously administered products included for Drug use for unknown indication: Pfizer/BioNTech (Dose Number: 1 Batch/Lot No: EN6201 Location of injection: Arm Right Vaccine Administration Time: 11:15 AM) on 26-Feb-2021, Pfizer/BioNTech (Dose number: 2 Batch/Lot No: EW0187 Location of injection: Arm Right Vaccine Administration Time: 02:30 PM) on 27-Aug-2021 and Pfizer/BioNTech (Dose number: 3 Batch/Lot No: EN6208 Location of injection: Arm Right Vaccine Administration Time: 11:45 AM) on 19-Mar-2022. Past adverse reactions to the above products included No adverse event with Pfizer/BioNTech, Pfizer/BioNTech and Pfizer/BioNTech. Concurrent medical conditions included Drug allergy (Unknown drug). On 30-Mar-2022 at 2:45 PM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In March 2022, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient took Pfizer dose 3 on 19-Mar-2022 and Moderna dose 4 on 30-Mar-2022). On 18-May-2022 at 11:00 AM, the patient experienced OROPHARYNGEAL PAIN (sore throat), EYE PAIN (eye aches), INSOMNIA (difficulty sleeping), FATIGUE (Extreme fatigue), MYALGIA (body aches), CHILLS (chills) and HEADACHE (headaches). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient took Pfizer dose 3 on 19-Mar-2022 and Moderna dose 4 on 30-Mar-2022), OROPHARYNGEAL PAIN (sore throat), EYE PAIN (eye aches), INSOMNIA (difficulty sleeping), FATIGUE (Extreme fatigue), MYALGIA (body aches), CHILLS (chills) and HEADACHE (headaches) outcome was unknown. No concomitant medications were reported. The patient previously received a COVID-19 Vaccine. It was unknown that the patient was taking any other medications/products within 2 weeks of starting COVID-19 treatment. The patient had treatment for COVID-19 (unspecified). Device Date: 21-May-2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy (Unknown drug)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 19.01.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 18,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Gait disturbance
Movement disorder
Musculoskeletal stiffness
Myalgia
Pain
Pain in extremity
Swelling
Symptomtext
It came on as soon as I woke up. I was very stiff and sore. I couldn't move my hands. My feet were sore especially the balls of my feet, it was painful to walk. My leg and arm muscles were very painful. For about a week I thought it would get better on its own. After two weeks I decided to contact my doctor, I wasn't able to get in until a month later. I took Tylenol and Ibuprofen to help with the swelling but it just kept coming back. When I finally saw the doctor, he gave me a 3-day supply of prednisone which worked well but a couple days after I had to start taking the Tylenol and ibuprofen to help the pain. As of today, I am still taking the medications for the pain and swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- Blood work
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression; Heart disease
- Andere Medikamente
- Aspirin Multivitamin Vitamin D3 Venlafaxine Omeprazole
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Dysstasia
Fatigue
Joint effusion
Joint stiffness
Magnetic resonance imaging joint
Peripheral swelling
Symptomtext
Within 8-10 hours after the vaccine I had an onset of extreme Fatigue and Joint Pain, I have no recollection of 72 hours post vaccine. After which my left knee blew up with fluid, swollen fingers, wrist pain and stiff ankles. I was given glutathione injection to help with stiffness. In addition I tried Homeopathic therapy and nothing has helped. It takes me a long time to get up from a sitting position and I cannot stand for long periods of time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- MRI conducted on Right Knee.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Synthroid, Progesterone, Claritin, Zyrtec, Vitamin D, Calcium
- Allergien
- Clindamycin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 24.04.2022
- Impfdatum
- 27.02.2022
- Beginn
- 27.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Urticaria
Symptomtext
PT STATES THEY HAVE LONG TERM TRANSIENT DERMALOGIC SIDE EFFECTS INCLUDING TRANSIENT LONG TERM HIVES, WELTS AND RASHES
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 22.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 16.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Asthenia
Chills
Fatigue
Myalgia
Pain
Symptomtext
The day after my booster vaccine that I started to feel symptoms of sore muscles, joint pain, chills, weakness, fatigue. No fever. The day after I was starting to feel better, however I still had body aches, muscles pain and fatigue. As of now I am feeling good and back to normal with a little bit of fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetic
- Andere Medikamente
- Pradaxa 150mg; Lisinopril twice a day 20 mg; Insulin Apidra 3x daily 5mg; Tojaio once daily 300mg; Cabergoline once a month
- Allergien
- Previnar-13; 65+ flu shot
- Vorherige Impfungen
- Previnar-13 2017-2018: ER visit due to rash, chills, muscle aches. 65+ flu shot: Rash development and itching.
- Staat
- SC
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Head discomfort
Headache
Injection site warmth
Insomnia
Neck pain
Pain
Pain in extremity
Peripheral swelling
Pyrexia
Vomiting
Symptomtext
Dear Dr and Staff, I just wanted to report my reaction to the 2nd booster shot since it was remarkable. I need no further care, I just want to let you know. I am just fine now, however approximately 8-9 hours after I received the booster shot, my arm began to swell, hurt, and fell hot to the touch at the injection site. About 10-11 hours after, I began running a fever, and an excruciating headache set in. I get migraines and this "headache" was worse then a migraine - I felt similar pain to when I was 13 with mumps/encephalitis - it felt like there was increasing pressure all around my head, but especially on the left side of my head, the same side I received the booster on. I also felt pain on the left side of my neck, upper back, and left leg. My fever increased to 102 degrees, and at some point during the night I began vomiting, and continued to do so I think 3-4 times. I finally was able to return to bed, but the fever did not break until about 11:00 am the next day. Feeling like the vomiting had passed, I took an ibuprofen in the early morning (6 am), and the pain decreased to a dull pain feeling, and then disappeared by about 2 pm. I did not sleep during the night - it wasn't possible. I just wanted someone there to know. Ironically, I had received my last check-in from v-safe the day before this injection. My best to all,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- ?Propranolol HCl 10 MG Tablet 1 tablet Orally Twice a day prn palpitations or elevatedbp ?Vyvanse 60 MG Capsule 1 capsule in the morning Orally Once a day ?Amphetamine Sulfate 10 MG Tablet 1 tablet in the morning Orally Once a day
- Allergien
- Codeine Sulfate and Percocet
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 19.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Burning sensation
Lymph node pain
Pain in extremity
Symptomtext
I experienced pain in my right arm, and I experienced swollen painful/burning lymph nodes under my arm, which lasted for 4 or 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Spinal Stenosis; Ruptured Disc C3; Asthma; TMJ on the right
- Andere Medikamente
- Gabapentin, Cyclobenzaprine, Pravastatin Sodium, Montelukast Sodium, Ventolin Inhaler, Benzonate, Baby Aspirin, Vitamin B Complex, Men's Multivitamin, Metamucil, CoQ10
- Allergien
- Minocycline; Peanuts
- Vorherige Impfungen
- Covid19 Moderna dose 2 with body aches and fatigue 2/12/21
- Staat
- VA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 17.04.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Peripheral swelling
Rash
Swelling of eyelid
Symptomtext
This was a booster as I am immunocompromised. I received the Pfizer vaccines (2 doses and 1 booster) without any notable reactions before this dose of Moderna. My arm became very swollen and sore, I had a rash on my trunk and arms, and my eyelid became very swollen. My care provider prescribed a low dose of prednisone for another condition. I believe that this Rx also helped alleviate the adverse reaction to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- asplenia
- Andere Medikamente
- 88 mcg levothyroxine for hypothyroidism
- Allergien
- -
- Vorherige Impfungen
- I have had widespread rash after Pneumonococcal vaccine
- Staat
- WA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 23.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Pyrexia
Somnolence
Vaccination site discolouration
Vaccination site erythema
Vaccination site pruritus
Symptomtext
black spots at injection site; red spots started to appear at the injection site; fever; tiredness; slept the whole day; itching at the injection site; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE DISCOLOURATION (black spots at injection site), SOMNOLENCE (slept the whole day), VACCINATION SITE PRURITUS (itching at the injection site), VACCINATION SITE ERYTHEMA (red spots started to appear at the injection site) and PYREXIA (fever) in a 28-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J212A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19 (patient tested positive) in December 2021. Previously administered products included for Product used for unknown indication: Pfizer (Dose Number: 1, Lot number: EN6201, Expiration date: 30-Jun-2021) on 05-Mar-2021, Pfizer (Dose Number: 2, Lot number: EN6201 and Expiration date: 30-Jun-2021) on 26-Mar-2021. Past adverse reactions to the above products included No adverse event with Pfizer and Pfizer. On 23-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 24-Mar-2022, the patient experienced SOMNOLENCE (slept the whole day), VACCINATION SITE PRURITUS (itching at the injection site), PYREXIA (fever) and FATIGUE (tiredness). On 25-Mar-2022, the patient experienced VACCINATION SITE ERYTHEMA (red spots started to appear at the injection site). On 28-Mar-2022, the patient experienced VACCINATION SITE DISCOLOURATION (black spots at injection site). On 25-Mar-2022, SOMNOLENCE (slept the whole day), PYREXIA (fever) and FATIGUE (tiredness) had resolved. At the time of the report, VACCINATION SITE DISCOLOURATION (black spots at injection site) and VACCINATION SITE PRURITUS (itching at the injection site) had not resolved and VACCINATION SITE ERYTHEMA (red spots started to appear at the injection site) had resolved with sequelae. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that patient is not on any concomitant medications. It was reported that the black spots are about an inch in diameter. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (patient tested positive)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 25.03.2022
- Impfdatum
- 24.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Axillary pain
Oedema peripheral
Symptomtext
Subjective left axillary swelling and soreness, not appreciated on exam.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Lower back pain
- Vorgeschichte
- None
- Andere Medikamente
- Celebrex 100mg PO QDay
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blindness
Burning sensation
Deafness
Dizziness
Dysstasia
Feeling hot
Gait disturbance
Musculoskeletal stiffness
Pain
Pain in extremity
Pruritus
Pyrexia
Rash macular
Tenderness
Symptomtext
3/18 - shot given- slight burning and hot feeling pain/ tender in arm 3/19 - body aches/pains manageable with ibuprofen 3/20 - Severe body aches/pains and weakness. Unable to walk a short distance. Walking from bedroom to living room felt faint, everything went black and couldn't hear. Laid on floor until senses came back. Felt faint upon trying to walk for remainder of day. 102 fever throughout day, down to 101.5 with meds. So weak needed help sitting up from floor. Fever broke around 8pm. Then noticed injection site arm was red/blotchy and hot. 3/21 - Still weak and achy but no fever. Arm still blotchy, hot, itchy and sore/stiff 3/22 - Arm still blotchy, hot, itchy and sore/stiff
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Small Meningioma brain tumor
- Andere Medikamente
- Pre Natal vitamin 1x daily
- Allergien
- Celiac disease - No gluten or dairy
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 22.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blindness
Burning sensation
Deafness
Dizziness
Dysstasia
Feeling hot
Gait disturbance
Musculoskeletal stiffness
Pain
Pain in extremity
Pruritus
Pyrexia
Rash macular
Tenderness
Symptomtext
3/18 - shot given- slight burning and hot feeling pain/ tender in arm 3/19 - body aches/pains manageable with ibuprofen 3/20 - Severe body aches/pains and weakness. Unable to walk a short distance. Walking from bedroom to living room felt faint, everything went black and couldn't hear. Laid on floor until senses came back. Felt faint upon trying to walk for remainder of day. 102 fever throughout day, down to 101.5 with meds. So weak needed help sitting up from floor. Fever broke around 8pm. Then noticed injection site arm was red/blotchy and hot. 3/21 - Still weak and achy but no fever. Arm still blotchy, hot, itchy and sore/stiff 3/22 - Arm still blotchy, hot, itchy and sore/stiff
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Small Meningioma brain tumor
- Andere Medikamente
- Pre Natal vitamin 1x daily
- Allergien
- Celiac disease - No gluten or dairy
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 17.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Burning sensation
Pruritus
Urticaria chronic
Symptomtext
Chronic urticaria from January 31, 2022 to present. Scalp, face and body covered in hives every day; multiple times a day. Excessive itching/burning sensation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin and Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 16.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- OT / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Abdominal pain
Nausea
Pyrexia
Vomiting
Symptomtext
fever, abd pain, n/v
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 07.03.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Photopsia
Pyrexia
Vitreous detachment
Vitreous floaters
Symptomtext
White flashes in left eye, starting in the night of the booster (with fever), and subsequent dark floaters in left visual field. Symptoms did not resolve, and saw an ophthalmologist on February 3. Physician diagnosed a left vitreous detachment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Exam by ophthalmologist.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Lipoprotein(a) levels
- Andere Medikamente
- Clopidogrel
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- 15.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Pruritus
Urticaria
Symptomtext
On Feb 23rd I began experiencing intense itching and hives all over my body. It has been over 1 week and I am still experiencing itching throughout my body and dermatographia. The welts caused by light touch are very uncomfortable and add on to the already intense itching. Called my doctor and was ordered 5 days of prednisone, but experienced no relief. Started taking allegra and it makes the itching less intense and my skin less reactive touch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 03.03.2022
- Impfdatum
- 02.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Pain
Urticaria
Symptomtext
HIVES, REDNESS AT THE INJECTION SITE AND BODY ACHES
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discomfort
Fatigue
Hypersensitivity
Lip pruritus
Swelling of eyelid
Throat irritation
Tongue pruritus
Symptomtext
Patient had an allergic reaction to vaccine approximately 20-30 minutes from administration. Pt c/o itchy tongue, throat, lips and had visible swelling to eyelids. Denied difficulty breathing. Administered 50 mg/ml of Dipenhydramine IM and followed up with patient at 12:20 pm, she denied trouble breathing, stated she was no longer itching and only felt her tongue slightly heavy. C/o fatigue from the dipenhydramine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Vicodin
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Histamine intolerance
Mechanical urticaria
Pruritus
Sleep disorder
Symptomtext
Severe histamine intolerance. Onset of dermatographia and other dermatological concerns. Cannot sleep a full night because of itching skin with no rash or main point of irritation. Only reporting this here because the booster is the only thing I have taken that might have caused this. I don't take ibuprofen or other medications ever (I'm mostly into just letting my body run its course unless there's a pandemic!)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- Will be going to the dermatologist tomorrow to get blood work and possibly a biopsy on the affected areas to see if this is fungal. Will update you.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Eye pruritus
Mechanical urticaria
Pruritus
Sleep disorder
Urticaria
Symptomtext
Extremely itchy eyes, scalp, body. Very itchy hives on several area of my body randomly appearing on different areas all times of the day and night. At night it is worst. Dermographia that Itches and causes hives. It wakes me up during the night. Zyrtec does not help, Benadryl does not help, Claritin helped a little but not enough. My Doctor prescribed hydroxyzine HCl 10mg tonight will be my first time taking it. I also received a referral for an allergist. I'm awaiting approval.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- Today 2/24/22 my doctor had blood drawn to run tests.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 19.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthropod bite
Erythema
Pruritus
Rash macular
Skin discolouration
Skin irritation
Urticaria
Symptomtext
2 weeks later; I have developed hives all over my body. Lesser on my arms but a few individual hives on wrists, arms, hands. Some on the back on my scalp. A few have ranged under my chin and neck area but the primary location tends to be the base of my spine, my hips, the back of my legs, groin/pelvic region, and thighs. A few noted on calves, especially in the joint areas, behind the knees, elbows etc. The largest masses of hives tend to be along the belt area and extend down the legs from there. All are itchy and white/red depending on irritation. Hives appear splotchy and grouped in satellites; few are individual hives. Unbearably itchy. Note: I don't see anywhere requesting blood type. I am A+. This feels much like my severe reactions to mosquito bites. Same hives, same itch, just at a much larger scale. I am postulating there is a correlation of people experiencing these same reactions with those of a certain blood type; and I'm guessing it's type A.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 17.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blood test normal
Borrelia test negative
Dizziness
Ear pain
Headache
Impaired driving ability
Pain of skin
Pruritus
Pyrexia
Tinnitus
Urticaria
Vision blurred
Symptomtext
Fever. Large, painful, itchy skin hives all over scalp, forehead, cheeks, chin, neck, shoulders, abdomen and legs. Dizzy. Headaches. Earaches, ringing in the ear. Blurry vison. Difficulty driving. Started 01/17/2022 and still going on today 02/17/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Blood work done checking for Lyme's disease. Result - Negative.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Crestor (Rosuvastatin) 5 mg once daily. Started taking this on 01/04/2022 but stopped as of 01/31/2022 on doctor's advise due to reaction from Moderna COVID booster shot administered on 01/17/2022.
- Allergien
- -
- Vorherige Impfungen
- Flu vaccine administered on 10/24/2019. Age 57. side effects: Flu like symptoms (chills) lasted for 6 months.
- Staat
- MA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 22.01.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 17,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Urticaria
Symptomtext
Began w/urticarial rash on torso, upper and lower extremities, and scalp, on-going x4 days at time of evaluation. Symptoms began 17days after booster dose of COVID moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Physical exam
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- None
- Andere Medikamente
- NA
- Allergien
- shellfish, seasonal allergies
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Headache
Pruritus
Rash
Rash erythematous
Rash papular
Skin irritation
Urticaria
Symptomtext
Rash covering about half the body that's red, raised, and hives-like in certain areas. Areas included patient's arms, axillary area, breasts, sides, stomach, and back. The rash began the morning after administration of the vaccine and is extremely itchy and irritating. The patient sough emergency treatment for it. She also said she had a pounding headache that began the night of vaccine administration and had persisted for 3 days. Patient states she did not have any type of rash following the first or second doses of the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, High cholesterol, heart murmur, sleep apnea
- Andere Medikamente
- Finasteride 1mg, Amlodipine 5mg, Valsartan 320mg, Atorvastatin 40mg, Estradiol 0.025mg/day patch, Vitamin D2 50,000 unit
- Allergien
- Pregabalin, methimazole, peanuts
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 12.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Hypoaesthesia
Nausea
Symptomtext
Patient chief complaints were nausea, chills and numbness in finger tips and feet
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- DIABETES
- Andere Medikamente
- -
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 24.01.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Mechanical urticaria
Pruritus
Urticaria
Symptomtext
Got 3 covid shots - First shot 04/23/2021 - Second shot 05/21/2021 - Booster shot 01/24/2021 About 12 days after my booster shot, I got extremely itchy. This led to redness and hives. Running my nail softly over skin will cause a red mark to appear a couple minutes later and will disappear eventually. I believe I have developed Dermatographia. I have been using Claritin and using Cortizone on extreme spots.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Feeling abnormal
Headache
Muscle rigidity
Skin burning sensation
Symptomtext
per pt. had severe headache and feeling of "skin burning sensation" and he sensed feeling of muscle rigidity . was told go to er he called them and they told him that could take some time for reaction to subside and they were 6 hour wait so he chose not to go in took allergy medication . we called pt. 2/9 and pt. said still didnt feel right but was better
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- none disclosed by pt.
- Andere Medikamente
- unknown
- Allergien
- pcn
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Fatigue
Headache
Pyrexia
Rash
Rash pruritic
Symptomtext
Patient received the COVID-19 vaccine #1 (Moderna; Lot: 016J212A) on 5 February 2022 on her R upper arm a medical facility. She received the vaccine around 0930. She noted in 10 minutes feeling lightheaded. She was monitored by medical staff at the facility with reported systolic BP of 92. She remained in the clinic for one hour and was discharged. She reported no loss of consciousness or immediate rash or swelling. She went home and to bed at noon and awoke at 1400 and noticed rash on both upper arms and on the R side of her neck. The rash was itching and persisted on her arms and gradually resolved by 7 Feb 2022 without treatment given. She also noted after awakening at noon on 5 February 2022, persistent feeling of lightheadedness, fatigue and headache. She noted the evening of 5 February a low grade fever of 99.8. These symptoms persisted through 8 February 2022 with all symptoms resolved by 9 February 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Fibromyalgia, migraines, insomnia
- Andere Medikamente
- Pregalalin, Rimegepant as needed for migraines, Botox for migraines
- Allergien
- allergic reaction to past influenza vaccine
- Vorherige Impfungen
- influenza in 2003, fatigue, shortness of breath, vomiting, passed out
- Staat
- WI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 29.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Chills
Dizziness
Symptomtext
Patient presented for a vaccine at our clinic. According to her husband, three years ago, she underwent stem cell treatment for lymphoma and has had a history of reactions after obtaining various vaccines. According to LPN, patient appeared anxious and asked several questions prior to being vaccinated. After the administration, patient asked what she should do if she felt post-vaccine sideaffects and expressed concern about going to a hospital due to COVID census being reported in the news. She ambulated to the observation area of the clinic under her own power and did not appear to have any problems. Beginning approximately 15 minutes in the observation area, she notified clinic observation staff that she felt dizzy. Staff assisted her to a treatment cot and obtained vital signs. Patient as given juice and water to drink which she did, and rested. Serial vital signs were obtained. At least another 15 minutes later, patient later complained of "a weight on her chest", and chills. She had her eyes closed and was slower to answer questions. EMS was notified and patient required assistance to be lifted onto the stretcher by EMS and clinic staff. Patient was transported to Hospital for further treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Transported to Hospital for further evaluation
- Aktuelle Erkrankungen
- Lymphoma
- Vorgeschichte
- Lymphoma Received stem cell treatments approximately 3 years prior
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 06.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Fatigue
Nausea
Symptomtext
Improving abdominal pain, fatigue, and nausea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- none
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Pt reported only experiencing generalized rash to back. No acute respiratory problem and/or complaints voiced during assessment. Advised to notify PCP immediately. Also advised the CDC/ADPH recommendation to take OTC Benadryl as directed to alleviate symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- Gout, HTN.
- Vorgeschichte
- Patient reported none.
- Andere Medikamente
- Client state gout and HTN medication. Unable to recall names during assessment.
- Allergien
- NKDA, NKEA.
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 06.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Erythema
Fatigue
Headache
Injection site induration
Nausea
Neck pain
Nodule
Pain in extremity
Peripheral swelling
Skin warm
Vision blurred
Symptomtext
The morning after I received the Covid vaccine my arm was super sore which was to be expected. But as I?m going about my day, I start to notice the pain was increasing more and more to where it felt like I had a rock or something under my skin. I looked and felt my arm and it was VERY HOT to the touch, super red, and it was the biggest knot ever! Plus my whole upper arm was like a huge hump and extremely swollen. But at the injection site, it felt like a hard medium sized rock was under my skin and when I moved my arm at all or got dressed even, the pain was very extreme. Following the rest of the day, I start noticing that my back and neck began to get sore. I thought nothing of it until it became a nagging pain and I had to sit down and rest and try to relieve the pain. I also have been slightly nauseas and very tired since the day after I received the vaccine. Last thing I noticed was my head pounding. I got such a severe headache that my eyes started to get blurry and they still are. My arm is still very sore as well, but my nausea has subsided for now. It?s only been going on two days post vaccine so we?ll see how long these symptoms last.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Covid 19 positive 3 weeks before administered vaccine
- Vorgeschichte
- Chronic Kidney stones Asthma Spinal stenosis Barrett?s esophagus
- Andere Medikamente
- Bupenorphine IB profin Albuterol Inhaler Pantoprazole Venlafaxine
- Allergien
- Tetracycline Doxycycline Cipro
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Injection site pain
Pain
Pyrexia
Symptomtext
Fever, chills, generalized body aches and intense pain at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- PCN; Sulfa
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 05.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Fatigue
Headache
Pain
Pain in extremity
Tinnitus
Symptomtext
Moderna booster was administered 1/19/22 around 530 pm. Body pain and fatigue started approximately 4 hours later. Within the first 24 hours headache, tinnitus, body pain, joint pain, fatigue, weakness and arm pain at injection site.. These symptoms lasted approximately 48-72 hours. HOWEVER, THE TINNITUS HAS CONTINUED ON A DAILY BASIS AND HAS NOT RESOLVED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Asthma
- Andere Medikamente
- Albuterol MDI (PRN) Breo Inhaler (PRN)
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Dizziness
Symptomtext
IT WAS ADDITIONAL DOSE FOR MODERNA, AFTER 10 MINUTES PT FELT DIZZY, BLOOD PRESSURE WAS 220/100, PT WENT TO ER, BUT AFTER 2 TO 3 HOURES PT WAS OK
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Incorrect route of product administration
Vaccination site erythema
Vaccination site pain
Vaccination site pruritus
Vaccination site warmth
Symptomtext
a little bit tired; a little sore, still sore; vaccine not given in the right place, injection site half way between elbow and shoulder; huge bright red band of about 3 inches, huge bright red band across the injection site and the back of her arm, it?s fading, it?s more pink; hot; it itches; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE WARMTH (hot), VACCINATION SITE PRURITUS (it itches), VACCINATION SITE PAIN (a little sore, still sore), VACCINATION SITE ERYTHEMA (huge bright red band of about 3 inches, huge bright red band across the injection site and the back of her arm, it?s fading, it?s more pink) and FATIGUE (a little bit tired) in a 77-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included PROPRANOLOL, SIMVASTATIN, ASCORBIC ACID, ERGOCALCIFEROL, NICOTINAMIDE, RETINOL, RIBOFLAVIN, THIAMINE HYDROCHLORIDE (VITAMINS [ASCORBIC ACID;ERGOCALCIFEROL;NICOTINAMIDE;RETINOL;RIBOFLAVIN;THIAMINE HYDROCHLORIDE]), ESOMEPRAZOLE MAGNESIUM (NEXIUM [ESOMEPRAZOLE MAGNESIUM]), ASPIRIN [ACETYLSALICYLIC ACID], BIFIDOBACTERIUM LONGUM, LACTOBACILLUS ACIDOPHILUS, LACTOBACILLUS RHAMNOSUS (PROBIOTICS [BIFIDOBACTERIUM LONGUM;LACTOBACILLUS ACIDOPHILUS;LACTOBACILLUS RHAMNOSUS]) and CELECOXIB (CELEBREX) for an unknown indication. On 19-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In January 2022, the patient experienced VACCINATION SITE WARMTH (hot), VACCINATION SITE PRURITUS (it itches) and VACCINATION SITE ERYTHEMA (huge bright red band of about 3 inches, huge bright red band across the injection site and the back of her arm, it?s fading, it?s more pink). On 19-Jan-2022, the patient experienced INCORRECT ROUTE OF PRODUCT ADMINISTRATION (vaccine not given in the right place, injection site half way between elbow and shoulder). On 20-Jan-2022, the patient experienced VACCINATION SITE PAIN (a little sore, still sore). On an unknown date, the patient experienced FATIGUE (a little bit tired). On 19-Jan-2022, INCORRECT ROUTE OF PRODUCT ADMINISTRATION (vaccine not given in the right place, injection site half way between elbow and shoulder) had resolved. At the time of the report, VACCINATION SITE WARMTH (hot), VACCINATION SITE PRURITUS (it itches), VACCINATION SITE ERYTHEMA (huge bright red band of about 3 inches, huge bright red band across the injection site and the back of her arm, it?s fading, it?s more pink) and FATIGUE (a little bit tired) outcome was unknown and VACCINATION SITE PAIN (a little sore, still sore) had not resolved. Treatment medications were not reported. It was a little sore the next day, and then had a huge bright red band of about 3 inches across the injection site and the back of her arm, it was hot. The patient went to the doctor, who told her that the vaccine was not given in the right place. The injection site was half way between the elbow and the shoulder, and the doctor told her it was supposed to be higher up. Now the arm was still sore, it was not red but was fading, more pink, and it itches and was a little bit tired. No medical history were reported. This case was linked to MOD-2022-466487, MOD-2022-466488 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- PROPRANOLOL; SIMVASTATIN; VITAMINS [ASCORBIC ACID;ERGOCALCIFEROL;NICOTINAMIDE;RETINOL;RIBOFLAVIN;THIAMINE HYDROCHLORIDE]; NEXIUM [ESOMEPRAZOLE MAGNESIUM]; ASPIRIN [ACETYLSALICYLIC ACID]; PROBIOTICS [BIFIDOBACTERIUM LONGUM;LACTOBACILLUS ACID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Malaise
Muscle spasms
Oropharyngeal pain
Somnolence
Taste disorder
Symptomtext
Woke up during the night with cramps in my legs (calf) and left arm. In the am, I was extremely tired, ~ sore throat ~ bad headache ~, sleeping on and off ~ muscles still cramping up ~ odd taste in my mouth. Just not feeling well ~ daughter (nurse) suggested it was from the vaccine and should report this
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Allergies, seasonal and some sents
- Andere Medikamente
- Sertraline 20mg Pantoprazole SOD 40mg Cyclobenzapr 10 mg, 30 tablets last 6 months Bayer 81 mg Stool Softener Magnesium D3 1000iu Zinc 50 mg
- Allergien
- Pencillin Sulfa sour cream, mayo
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Rash pruritic
Symptomtext
Seen at ER on 1/28/22 Dr with itchy rash on wrists bil up to upper arms bil and under arm pit region, rash began on 1/26/22, no resp. distress, afebrile, received 3rd dose COVID-19 vaccine on 1/14/22 , MR notes rash appears to be consistent with uticaria multiforme vs serum sickness, recommended refraining from getting future boosters. IM Benadyl 50mg given in ER, prescribed Cetirizne PO 10 mg daily, discharged home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash pruritic
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Patient develops a moderate to severe dizziness after five minutes receiving the shot for 15 minutes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- NA
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 29.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Induration
Rash
Skin warm
Swelling
Symptomtext
SWOLLEN/HARD AREA, WARM TO TOUCH AND RASH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Symptomtext
Swollen, painful lymph node under left arm pit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Obesity (BMI >41), anemia, sciatica, arthritis in both knees and ankles, Desmoid tumor at C3-C4, and seasonal allergies
- Andere Medikamente
- Ferrous iron infusion (intraveneous drip) on 1/27/22 at 3pm due to chronic anemia 1/28/2022 at 7am: 40mg prilosec, 20mg Claritin, 17.5mg Phentermine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 27.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Pruritus
Symptomtext
extreme fatigue, headache and Itching all over he body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none yet
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- unknown
- Allergien
- no known drug allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site rash
Injection site swelling
Injection site warmth
Symptomtext
Received Moderna booster (1/18/22) and next day (1/19/22) rash noticed on left upper arm. In a.m. 1/20/22, patient came to Health office. Solid redness with slightly darker pin point dots covered left upper arm; area measured 7 inches X 8 Inches, warm to touch and slightly swollen, itchy. Patient took 25 mg tab Benadryl evening of 1/19/22 with no improvement. No other symptoms reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Blood pressure increased
Heart rate increased
Nausea
Vomiting
Symptomtext
At approximately 1310 patient returned to vaccine clinic after being discharged. Patient came in reporting an onset of symptoms that included an episode of emesis X1, abdominal pain and nausea 20 min post vaccination. Patient reported pain level of a 9 from pain scale of 0 to 10. Upon arrival patient vitals were taken. Refer to chart. Patient was assessed for signs and symptoms of anaphylaxis. Patient was alert and oriented X4, patient denied shortness of breath dizziness and lightheadedness. SpO2 at 100% at Room Air. Doctor, allergist on call was called to report the patient's symptoms. Doctor recommended patient be monitored for worsening symptoms for an additional 30 min. After being monitored for 30 min patient reported a decrease in pain from a 9 to a 3. Although patient pain level decreased patient continued to have elevated BP and HR. Patient was referred to NP on site to be more closely evaluated. Dr. was notified that patient was referred to NP on site for further evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- latex and keflex
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Oedema peripheral
Pruritus
Tenderness
Urticaria
Symptomtext
DAY 2 AFTER VACCINE SIGNIFICANT SWELLING/TENDERNESS OF LEFT AXILLA. ON DAY 9 SIGNIFICANT HIVES/ITCHING STARTED ALL OVER BODY (HEAD,NECK,CHEST,ABDOMEN,LOWER EXTREMITIES) UNRELIEVED BY OVER THE COUNTER ANTIHISTAMINES. SEEN BY PRIMARY CARE TODAY.PRESCRIBED 10 DAY COURSE OF ORAL STEROIDS AND ADDITIONAL ANTIHISTAMINES. NO RECENT CHANGES IN HEALTH,MEDICATIONS,PRODUCTS OR DIET. NO KNOWN ALLERGIES.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Ocella (oral contraceptive)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dizziness
Headache
Pruritus
Skin warm
Symptomtext
Patient had complaints of headache, dizziness, slight itching and feeling warm. Pt was taken to ED for further assessment. Reaction occurred <15min after COVID vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Bipolar disorder, hypertension, hypothyroidism, migraine, IBS,
- Andere Medikamente
- n/a
- Allergien
- amoxicillin, azithromycin, Pfizer COVID vaccine, Moderna COVID Vaccine (added today 1/26/22), erythromycin, latex, morphine, pencillins, sulfa
- Vorherige Impfungen
- Headache, Dizziness, feeling warm, itchiness, and swollen arm
- Staat
- PA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental underdose
Arthralgia
Fatigue
Feeding disorder
Headache
Hyperhidrosis
Inappropriate schedule of product administration
Myalgia
Nausea
Pain
Symptomtext
patient is immunocompromised and received booster dose of vaccine; Inappropriate schedule of vaccine administered; Sweating in bed for 24 hours; Terrible terrible pain; Could not eat; Headache; Nausea so she could not eat; Joint pain; Muscle pain; woke up very tired but still went to work, big mistake; This spontaneous case was reported by a consumer and describes the occurrence of HYPERHIDROSIS (Sweating in bed for 24 hours), PAIN (Terrible terrible pain), FEEDING DISORDER (Could not eat), HEADACHE (Headache) and NAUSEA (Nausea so she could not eat) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19 (Patient felt worse when had COVID.) in October 2021. Previously administered products included for Product used for unknown indication: Johnson and Johnson (Lot Number (206A21A) and Arm of injection: Right) on 11-May-2021. Past adverse reactions to the above products included No adverse event with Johnson and Johnson. Concurrent medical conditions included Thyroid disorder, Cancer and Depression. Concomitant products included VENLAFAXINE HYDROCHLORIDE (EFFEXOR) for Antidepressant therapy, CANDESARTAN for Blood pressure, TAMOXIFEN for Cancer, LEVOTHYROXINE for Thyroid disorder, VITAMIN D3 and MULTIVITAMIN [VITAMINS NOS] for an unknown indication. On 20-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In January 2022, the patient experienced HYPERHIDROSIS (Sweating in bed for 24 hours), PAIN (Terrible terrible pain), FEEDING DISORDER (Could not eat), HEADACHE (Headache), NAUSEA (Nausea so she could not eat), ARTHRALGIA (Joint pain), MYALGIA (Muscle pain) and FATIGUE (woke up very tired but still went to work, big mistake). On 20-Jan-2022, the patient experienced ACCIDENTAL UNDERDOSE (patient is immunocompromised and received booster dose of vaccine) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) at an unspecified dose and frequency. On 20-Jan-2022, ACCIDENTAL UNDERDOSE (patient is immunocompromised and received booster dose of vaccine) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) had resolved. At the time of the report, HYPERHIDROSIS (Sweating in bed for 24 hours), PAIN (Terrible terrible pain), FEEDING DISORDER (Could not eat), ARTHRALGIA (Joint pain), MYALGIA (Muscle pain) and FATIGUE (woke up very tired but still went to work, big mistake) had resolved and HEADACHE (Headache) and NAUSEA (Nausea so she could not eat) had not resolved. Patient got the antibodies which is why Patient waited 90 more days before getting booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Cancer; Depression; Thyroid disorder.
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19 (Patient felt worse when had COVID.)
- Andere Medikamente
- CANDESARTAN; LEVOTHYROXINE; TAMOXIFEN; EFFEXOR; VITAMIN D3; MULTIVITAMIN [VITAMINS NOS.]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Exposure via breast milk
Fatigue
Headache
Injection site pain
Muscular weakness
Oropharyngeal pain
Pyrexia
Symptomtext
Fever: 105F going up and down; chills; sore throat; headache; muscle weakness; pain at site of the shot; fatigue. I?m breastfeeding and my baby got fever too.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Peripheral swelling
Pruritus
Symptomtext
Pt received Moderna booster and complains of swelling and itching around her entire upper arm. She has used hydrocortisone cream to help with the itching.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site erythema
Vaccination site pruritus
Vaccination site reaction
Symptomtext
Injection site reaction; injection site on her upper arm is red, itchy, big and round; injection site on her upper arm is red,itchy, big and round; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE REACTION (Injection site reaction), VACCINATION SITE PRURITUS (injection site on her upper arm is red, itchy, big and round) and VACCINATION SITE ERYTHEMA (injection site on her upper arm is red,itchy, big and round) in an 81-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Flu vaccine. Past adverse reactions to the above products included No adverse event with Flu vaccine. On 14-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Jan-2022, the patient experienced VACCINATION SITE REACTION (Injection site reaction), VACCINATION SITE PRURITUS (injection site on her upper arm is red, itchy, big and round) and VACCINATION SITE ERYTHEMA (injection site on her upper arm is red,itchy, big and round). At the time of the report, VACCINATION SITE REACTION (Injection site reaction), VACCINATION SITE PRURITUS (injection site on her upper arm is red, itchy, big and round) and VACCINATION SITE ERYTHEMA (injection site on her upper arm is red,itchy, big and round) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medication was reported. No treatment medication was reported. Patient had not applied anything on the site of reaction. Patient never had a reaction to the flu vaccine. Patient was scared to proceed. Second dose due on 11 Feb 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Symptomtext
patient reported soreness in her arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- no
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 17.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymph node pain
Lymphadenopathy
Symptomtext
Given Moderna Booster Shot. About a day after I received the booster shot, my left armpit lymph nodes had become swollen and painful. I am currently letting the swelling go down naturally, and will get medical treatment if it doesn't recover.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Headache
Injection site pain
Pain
Symptomtext
This was a booster. Area for the booster sore, headache, then full body aches, severe chills and dizziness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Sinus issue
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Additional Details: pt felt dizzy so we called the paramedics immediately. Even though her symptoms were resolve after 5 minutes, we still waited for the paramedic to make sure she was clear to leave. EMT cleared her after their assessment
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 15.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Urticaria
Symptomtext
Patient had previously received Pfizer for his primary 2 shots. Today 1/15/2022 the patient came in for a booster shot and elected for Moderna. Patient waited the recommended 15 minutes and at the end of this time he reported to pharmacy staff "I think I am having a reaction". When asked what type of reaction he pulled up his shirt and showed that a patch of hives was developing on the right side of his abdomen. Liquid diphenhydramine was administered and the patient waited on the pharmacy bench for a few minutes. After a few more minutes he said I think I am good and prepared to leave. The patient denied any other symptoms or any history of allergic reactions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
Patient reported feeling dizzy and lightheaded a few minutes after receiving vaccine while she was sitting in our post-vaccination waiting area. I went out to check on her, she was sitting with her eyes closed and leaning onto the back of the chair. I told her to stay still and let me know if she needed anything else. I gave her some water to drink while she was there, she stated not eating or drinking much prior to vaccine. She sat for about 10 minutes after that taking some sips of water until she reported feeling better. I asked her to wait about 5 more minutes before she got up just to make sure, and finally she was feeling all the way better and able to leave on her own. No medical treatment was needed, just water and time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Symptomtext
Red, swollen around injection site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 08.07.2023
- Impfdatum
- 06.05.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
THE SHOT WAS GIVEN 05/06/22.. BUT ON 6/28/23 WE WERE NOTIFIED THAT THE EXPIRATION DATE OF THE VACCINE REPORTED TO BE GIVEN WAS 4/17/22?? THE PHARMACY HAS NO WAY TO PROVE THAT THIS WAS OR WAS NOT CORRECT SINCE IT HAPPENED 1 AND 1/2 YEARS AGO
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 14.06.2023
- Impfdatum
- 07.03.2022
- Beginn
- 11.08.2022
- Tage bis Beginn
- 157,0
- Dosis
- 3
- 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 3 vaccines Moderna 2/15/21 lot# 031L20A; Moderna 3/15/21 lot# 030A21A; Moderna 3/7/22 lot# 016J212A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 26.04.2023
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19 immunisation
Off label use
Suspected COVID-19
Symptomtext
SUSPECTED COVID-19 INFECTION; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; OFF LABEL DOSING FREQUENCY; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a 62 year old male. The patient's height, and weight were not reported. The patient's concurrent conditions included: allergy. The patient was previously treated with Pfizer BionTech (tozinameran) (Dose number in series 1) (form of admin, route of admin were not reported, batch number:1805020 expiry: UNKNOWN) dose was not reported, administered on 18-MAR-2021 for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with Pfizer BionTech (tozinameran) (Dose number in series 1). The patient was previously treated with covid-19 vaccine ad26. cov2. s (Dose number in series 2) (suspension for injection, route of admin not reported, batch number: 1805020 expiry: UNKNOWN) dose was not reported, 1 total administered on 13-MAY-2021 for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with covid-19 vaccine ad26. cov2. s (Dose number in series 2). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 3) (suspension for injection, route of admin not reported, batch number: 1822809 expiry: UNKNOWN) dose was not reported, 1 total administered on 23-OCT-2021 for covid-19 prophylaxis which was associated with off label dosing frequency. The product was associated with Off label use (Dose number in series 3). Age at time of vaccination 62 years old. No concomitant medications were reported. The patient also received non-company suspect vaccine Moderna (elasomeran) (Dose number in series 4) (form of admin, route of admin were not reported, batch number: 016J21-2A expiry: UNKNOWN) dose was not reported, administered on 01-APR-2022 for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with Moderna (elasomeran) (Dose number in series 4). The patient additionaly received non-company suspect vaccine Moderna (elasomeran) (Dose number in series 5) (form of admin, route of admin were not reported, batch number: AS7162B expiry: UNKNOWN) dose was not reported, administered on 22-SEP-2022 for covid-19 prophylaxis which was revaccination with different covid-19 vaccine (Dose number in series 5). On an unspecified date in 2023, the patient experienced suspected covid-19 infection (Dose number in series 5) for which the patient was treated with non-company suspect drug Paxlovid (nirmatrelvir/ritonavir) (form of admin, route of admin, batch number and expiry date were not reported) dose and frequency were not reported from 05-APR-2023 to 09-APR-2023 for covid-19 treatment. On 15-APR-2023, the patient experienced rebound covid after paxlovid (Dose number in series 5). The action taken with covid-19 vaccine ad26.cov2.s, elasomeran, and elasomeran was not applicable; and action taken with nirmatrelvir/ritonavir was not reported. The outcome of the suspected covid-19 infection, off label dosing frequency and revaccination with different covid-19 vaccine was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 immunisation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy
- Vorgeschichte
- -
- Andere Medikamente
- PAXLOVID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 27.12.2022
- Impfdatum
- 14.01.2021
- Beginn
- 09.11.2022
- Tage bis Beginn
- 664,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Blood glucose increased
COVID-19
Mental status changes
SARS-CoV-2 test positive
Symptomtext
11/09/22 presents to ED for "altered mental status" "high blood sugar". PMHx of "HTN, and DM II"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood glucose increased
- Hospital-Tage
- -
- Labordaten
- 11/09/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 07.05.2021
- Beginn
- 01.10.2022
- Tage bis Beginn
- 512,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Gastrointestinal haemorrhage
Symptomtext
ADMISSION DIAGNOSIS: 1. COVID-19. 2. Gastrointestinal bleed. GI has deferred endoscopy to outpatient. 3. End-stage renal disease via left arm AV fistula Monday, Wednesday, Friday, ??. 4. Coronary artery disease, sees Dr. 5. Hypertension. 6. Diabetes. 7. Hyperlipidemia. 8. Ex-smoker. DISCHARGE DIAGNOSIS: 1. COVID-19. 2. Gastrointestinal bleed. GI has deferred endoscopy to outpatient. 3. End-stage renal disease via left arm AV fistula Monday, Wednesday, Friday, ?. 4. Coronary artery disease, sees Dr. 5. Hypertension. 6. Diabetes. 7. Hyperlipidemia. 8. Ex-smoker. The patient feels well. The patient completed his 3-day of remdesivir. If the patient is non hypoxic, the patient can be discharged after dialysis today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 10/1 SARS-CoV-2 -COVID-19 by NAA, Micro -- detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 30.11.2022
- Impfdatum
- 08.02.2022
- Beginn
- 28.11.2022
- Tage bis Beginn
- 293,0
- Dosis
- 3
- 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 3 vaccines Unknown type 3/19/21 Lot# 046A21A; Moderna 4/16/21 Lot# 043B21A; Moderna 2/8/22 LOt# 016J21-2A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 31.10.2022
- Impfdatum
- 18.06.2021
- Beginn
- 23.10.2022
- Tage bis Beginn
- 492,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
Pt admitted to hospital with COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 30.08.2022
- Impfdatum
- 28.01.2022
- Beginn
- 10.08.2022
- Tage bis Beginn
- 194,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Inappropriate schedule of product administration
SARS-CoV-2 antibody test
Symptomtext
Dry cough/Persistent dry cough; received 2 dose more than 35 days after 1st dose; This spontaneous case was reported by a consumer and describes the occurrence of COUGH (Dry cough/Persistent dry cough) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (received 2 dose more than 35 days after 1st dose) in a 28-year-old male patient who received mRNA-1273 (Spikevax) (batch nos. 052BZZA and 016J212A) for COVID-19 prophylaxis. Patient had no known allergies. No other vaccines were given within 1 month prior to Moderna COVID-19 vaccine. The patient's past medical history included COVID-19 in 2021 and Skin disorder. Concomitant products included PARACETAMOL (TYLENOL) and NAPROXEN SODIUM (ALEVE) for Headache. On 28-Jan-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) .5 milliliter. On 10-Aug-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to .5 milliliter. On 10-Aug-2022, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (received 2 dose more than 35 days after 1st dose). On 11-Aug-2022, the patient experienced COUGH (Dry cough/Persistent dry cough). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) at an unspecified dose and frequency and PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, COUGH (Dry cough/Persistent dry cough) had not resolved and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (received 2 dose more than 35 days after 1st dose) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In 2021, SARS-CoV-2 antibody test: (Positive) Positive. It was reported that they tried to get patient vaccinated sooner but were not able to. Patient had COVID test before vaccines in Summer of 2021. Not hospitalized, was sick for 2 weeks. Symptoms lasted 2 weeks, however, cough lingered for 1 month.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- -
- Labordaten
- Test Date: 2021; Test Name: COVID test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19; Skin disorder; Comments: Patient had no known allergies. No other vaccines were given within 1 month prior to Moderna COVID-19 vaccine.
- Andere Medikamente
- TYLENOL; ALEVE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 13.02.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 151,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Caller got a 3rd booster today 14Jul2022 of Moderna.; This spontaneous case was reported by a patient and describes the occurrence of EXTRA DOSE ADMINISTERED (Caller got a 3rd booster today 14Jul2022 of Moderna.) in a 71-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 0171322A and 016J212A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer (Dose 1), Pfizer (1st booster dose) and Pfizer (Dose 2). Past adverse reactions to the above products included No adverse event with Pfizer, Pfizer and Pfizer. Concurrent medical conditions included Immunocompromised. On 13-Feb-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Jul-2022, received fifth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 14-Jul-2022, the patient experienced EXTRA DOSE ADMINISTERED (Caller got a 3rd booster today 14Jul2022 of Moderna.). At the time of the report, EXTRA DOSE ADMINISTERED (Caller got a 3rd booster today 14Jul2022 of Moderna.) outcome was unknown. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Immunocompromised
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 20.07.2022
- Impfdatum
- 18.01.2022
- Beginn
- 07.07.2022
- Tage bis Beginn
- 170,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Conjunctivitis
Eye irritation
Lacrimation increased
Ophthalmological examination normal
Photophobia
Symptomtext
Bilateral eye irritation, photophobia, increased lacrimation and conjunctivitis without discharge. Lasted 72 hours. Resolved with ophthalmologic steroid drops.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Conjunctivitis
- Hospital-Tage
- -
- Labordaten
- Eye examination: Negative for foreign bodies, corneal abrasions or lacerations.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Flonase, Claritin
- Allergien
- Codeine, cat dander, hay fever
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 14.01.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 46,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cyst
Dysmenorrhoea
Heavy menstrual bleeding
Ultrasound scan abnormal
Symptomtext
Normally I don't have a period and it started to come back heavy in March, Now it comes for 2 weeks at a time very heavy and painful and they are not on track to when they should be. I have had pain the last cycle, I went in and they told me there was a cyst and I have to see a gyno.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cyst
- Hospital-Tage
- -
- Labordaten
- Ultrasound, cyst.
- Aktuelle Erkrankungen
- COVID-19
- Vorgeschichte
- N/A
- Andere Medikamente
- NEXPLANON
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 25.06.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of POOR QUALITY PRODUCT ADMINISTERED (Administered vaccine after having two excursion for a total of 29 hours and 30 minutes) and PRODUCT TEMPERATURE EXCURSION ISSUE (The first temperature excursion lasted for 9 hours 45 minutes/The total amount of the excursion is 29 hours 30 minutes.) in a male patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Mar-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 04-Mar-2022, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (Administered vaccine after having two excursion for a total of 29 hours and 30 minutes). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (The first temperature excursion lasted for 9 hours 45 minutes/The total amount of the excursion is 29 hours 30 minutes.). At the time of the report, POOR QUALITY PRODUCT ADMINISTERED (Administered vaccine after having two excursion for a total of 29 hours and 30 minutes) and PRODUCT TEMPERATURE EXCURSION ISSUE (The first temperature excursion lasted for 9 hours 45 minutes/The total amount of the excursion is 29 hours 30 minutes.) outcome was unknown. Concomitant products were not provided. The vial was first punctured on 04-Mar-2022. The vial were not exposed to room temperature. The vial was stored only in freezer. The vial did undergo temperature excursion. The maximum 10.8 degree Fahrenheit and minimum 5.5 degree Fahrenheit were reached. The vial was not moved from freezer to refrigerator. The vial was found to be refrozen in the visual inspection. At least 1 vial was impacted. No previous excursions were seen. Treatment medications were not reported. This case was linked to MOD-2022-592504 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 25.06.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- 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
Product storage error
Symptomtext
Vaccine given 37days after refrigerator shelf life; Vaccine given 37days after refrigerator shelf life; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine given 37days after refrigerator shelf life) and PRODUCT STORAGE ERROR (Vaccine given 37days after refrigerator shelf life) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 prophylaxis. It was reported that patient had no known drug allergy. Concurrent medical conditions included Depressive disorder, Hypertensive (Hypertensive disorder), Osteoporosis, Lung cancer (malignant tumor of lung), Mental disorder, Osteoarthritis, Alcoholism and Bipolar disorder. Concomitant products included CLONAZEPAM, DULOXETINE, ERGOCALCIFEROL (VITAMIN D [ERGOCALCIFEROL]), FUROSEMID [FUROSEMIDE], METFORMIN HYDROCHLORIDE (METFORMIN ER), SULFADIAZINE SILVER (SSD), TRAMADOL and WARFARIN SODIUM (WARFARIN [WARFARIN SODIUM]) for an unknown indication. On 18-Mar-2022 at 2:43 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 18-Mar-2022 at 2:43 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine given 37days after refrigerator shelf life). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine given 37days after refrigerator shelf life). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine given 37days after refrigerator shelf life) and PRODUCT STORAGE ERROR (Vaccine given 37days after refrigerator shelf life) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No treatment medication reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Alcoholism; Bipolar disorder; Depressive disorder; Hypertensive (Hypertensive disorder); Lung cancer (malignant tumor of lung); Mental disorder; Osteoarthritis; Osteoporosis
- Vorgeschichte
- Comments: It was reported that patient had no known drug allergy.
- Andere Medikamente
- CLONAZEPAM; DULOXETINE; VITAMIN D [ERGOCALCIFEROL]; FUROSEMID [FUROSEMIDE]; METFORMIN ER; SSD; TRAMADOL; WARFARIN [WARFARIN SODIUM]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 25.06.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine given 37days after refrigerator shelf life; Vaccine given 37days after refrigerator shelf life; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine given 37days after refrigerator shelf life) and PRODUCT STORAGE ERROR (Vaccine given 37days after refrigerator shelf life) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 prophylaxis. It was reported that patient had no known drug allergy. Concurrent medical conditions included Depressive disorder, Hypertensive (Hypertensive disorder), Osteoporosis, Lung cancer (malignant tumor of lung), Mental disorder, Osteoarthritis, Alcoholism and Bipolar disorder. Concomitant products included CLONAZEPAM, DULOXETINE, ERGOCALCIFEROL (VITAMIN D [ERGOCALCIFEROL]), FUROSEMID [FUROSEMIDE], METFORMIN HYDROCHLORIDE (METFORMIN ER), SULFADIAZINE SILVER (SSD), TRAMADOL and WARFARIN SODIUM (WARFARIN [WARFARIN SODIUM]) for an unknown indication. On 18-Mar-2022 at 2:43 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 18-Mar-2022 at 2:43 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine given 37days after refrigerator shelf life). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine given 37days after refrigerator shelf life). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine given 37days after refrigerator shelf life) and PRODUCT STORAGE ERROR (Vaccine given 37days after refrigerator shelf life) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No treatment medication reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Alcoholism; Bipolar disorder; Depressive disorder; Hypertensive (Hypertensive disorder); Lung cancer (malignant tumor of lung); Mental disorder; Osteoarthritis; Osteoporosis
- Vorgeschichte
- Comments: It was reported that patient had no known drug allergy.
- Andere Medikamente
- CLONAZEPAM; DULOXETINE; VITAMIN D [ERGOCALCIFEROL]; FUROSEMID [FUROSEMIDE]; METFORMIN ER; SSD; TRAMADOL; WARFARIN [WARFARIN SODIUM]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 25.06.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- 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
Product use issue
Symptomtext
Vaccine was given 37 days after refrigerator shelf life; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was given 37 days after refrigerator shelf life) in a 26-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 prophylaxis. NKDA (no known drug allergies). Concurrent medical conditions included Depressive disorder and ADHD (Attention deficit hyperactivity disorder). Concomitant products included AMOXICILLIN, NAPROXEN and TRAZODONE for an unknown indication. On 18-Mar-2022 at 1:23 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 18-Mar-2022 at 1:23 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was given 37 days after refrigerator shelf life). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was given 37 days after refrigerator shelf life) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product use issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- ADHD (Attention deficit hyperactivity disorder); Depressive disorder
- Vorgeschichte
- Comments: NKDA (no known drug allergies)
- Andere Medikamente
- AMOXICILLIN; NAPROXEN; TRAZODONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 25.06.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product use issue
Symptomtext
Vaccine was given 37 days after refrigerator shelf life; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was given 37 days after refrigerator shelf life) in a 26-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 prophylaxis. NKDA (no known drug allergies). Concurrent medical conditions included Depressive disorder and ADHD (Attention deficit hyperactivity disorder). Concomitant products included AMOXICILLIN, NAPROXEN and TRAZODONE for an unknown indication. On 18-Mar-2022 at 1:23 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 18-Mar-2022 at 1:23 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was given 37 days after refrigerator shelf life). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was given 37 days after refrigerator shelf life) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product use issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- ADHD (Attention deficit hyperactivity disorder); Depressive disorder
- Vorgeschichte
- Comments: NKDA (no known drug allergies)
- Andere Medikamente
- AMOXICILLIN; NAPROXEN; TRAZODONE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 23.06.2022
- Impfdatum
- 18.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Fluid retention
Imaging procedure
Symptomtext
Per pt they got the first booster on 1/18/22 and since then they have had fluid retention in arm. pt stated he needed a report because his doctor and lawyer told him he needed surgery due to water in arm and that it was caused by the covid shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fluid retention
- Hospital-Tage
- -
- Labordaten
- Per pt he had imaging done a couple of weeks ago and has water in arm.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- diabetes
- Andere Medikamente
- unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 23.06.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
The first temperature excursion lasted for 9 hours 45 minutes/The total amount of the excursion is 29 hours 30 minutes.; Administered vaccine after having two excursion for a total of 29 hours and 30 minutes; This spontaneous case was reported by an other health care professional and describes the occurrence of POOR QUALITY PRODUCT ADMINISTERED (Administered vaccine after having two excursion for a total of 29 hours and 30 minutes) and PRODUCT TEMPERATURE EXCURSION ISSUE (The first temperature excursion lasted for 9 hours 45 minutes/The total amount of the excursion is 29 hours 30 minutes.) in a 48-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Mar-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 04-Mar-2022, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (Administered vaccine after having two excursion for a total of 29 hours and 30 minutes). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (The first temperature excursion lasted for 9 hours 45 minutes/The total amount of the excursion is 29 hours 30 minutes.). At the time of the report, POOR QUALITY PRODUCT ADMINISTERED (Administered vaccine after having two excursion for a total of 29 hours and 30 minutes) and PRODUCT TEMPERATURE EXCURSION ISSUE (The first temperature excursion lasted for 9 hours 45 minutes/The total amount of the excursion is 29 hours 30 minutes.) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vial was first punctured on 04-Mar-2022. The vial were not exposed to room temperature. The vial was stored only in freezer. The vial did undergo temperature excursion. The maximum 10.8 degree Fahrenheit and minimum 5.5 degree Fahrenheit were reached. The vial was not moved from freezer to refrigerator. The vial was found to be refrozen in the visual inspection. At least 1 vial was impacted. No previous excursions were seen. This case was linked to MOD-2022-592557 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 10.05.2022
- Beginn
- 10.05.2022
- 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
No adverse event
Symptomtext
Expired Vaccine given. No adverse events occurred
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 03.05.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Expired vaccine given. No adverse events
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Htn, Hyperlipidemia
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 22.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Expired vaccine given to patient. No adverse events
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product 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
- -
- Geschlecht
- U
- Eingang
- 09.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
The vials were frozen and underwent 4 temperature excursions total; 7 doses given from 5 vials were eventually punctured and used after the 2nd excursion; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (The vials were frozen and underwent 4 temperature excursions total) and POOR QUALITY PRODUCT ADMINISTERED (7 doses given from 5 vials were eventually punctured and used after the 2nd excursion) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (The vials were frozen and underwent 4 temperature excursions total) and POOR QUALITY PRODUCT ADMINISTERED (7 doses given from 5 vials were eventually punctured and used after the 2nd excursion). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (The vials were frozen and underwent 4 temperature excursions total) and POOR QUALITY PRODUCT ADMINISTERED (7 doses given from 5 vials were eventually punctured and used after the 2nd excursion) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. On 13-Jan-2022 the freezer got to 5.4F for 15 minutes, then returned to the appropriate temperature range. On 20-Jan-2022 the freezer got to 6.1F for 15 minutes, then returned to the appropriate temperature range. On 11-Feb-2022 the freezer got to 10.8F for 10 hours and 15 minutes overnight into 12-Feb-2022, then returned to the appropriate temperature range. On 25-Feb-2022 the freezer got to 22.6F and was out of range for 20 hours total into 26-Feb-2022 then returned to the appropriate temperature range. The storage condition at the time of the excursion was frozen. The vials were moved from freezer to refrigerator on 1 dose/vial on 30-Jan-2022. No visual inspection was done, noting any vaccine state change. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 09.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
Vials were frozen & underwent 4 temperature excursions; 7 doses given from 5 vials that underwent more than 1 temperature excursion; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vials were frozen & underwent 4 temperature excursions) and POOR QUALITY PRODUCT ADMINISTERED (7 doses given from 5 vials that underwent more than 1 temperature excursion) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vials were frozen & underwent 4 temperature excursions) and POOR QUALITY PRODUCT ADMINISTERED (7 doses given from 5 vials that underwent more than 1 temperature excursion). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vials were frozen & underwent 4 temperature excursions) and POOR QUALITY PRODUCT ADMINISTERED (7 doses given from 5 vials that underwent more than 1 temperature excursion) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. On 13Jan2022 the freezer got to 5.4F for 15 minutes, then returned to the appropriate temperature range. On 20Jan2022 the freezer got to 6.1F for 15 minutes, then returned to the appropriate temperature range. On 11Feb2022 the freezer got to 10.8F for 10 hours and 15 minutes overnight into 12Feb2022, then returned to the appropriate temperature range. On 25Feb2022 the freezer got to 22.6F & was out of range for 20 hours total into 26Feb2022 then returned to the appropriate temperature range. Date vial moved from freezer to refrigerator was 1dose/vial on 25Jan2022. Number of vials/doses impacted was 7 doses/5 vials. 5 vials were eventually punctured & used after the 2nd excursion. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 09.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
The vials were frozen and underwent 4 temperature excursions total; 7 doses given from 5 vials were eventually punctured and used after the 2nd excursion; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (The vials were frozen and underwent 4 temperature excursions total) and POOR QUALITY PRODUCT ADMINISTERED (7 doses given from 5 vials were eventually punctured and used after the 2nd excursion) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (The vials were frozen and underwent 4 temperature excursions total). an unknown date, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (7 doses given from 5 vials were eventually punctured and used after the 2nd excursion). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (The vials were frozen and underwent 4 temperature excursions total) and POOR QUALITY PRODUCT ADMINISTERED (7 doses given from 5 vials were eventually punctured and used after the 2nd excursion) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. On 13-Jan-2022 the freezer got to 5.4F for 15 minutes, then returned to the appropriate temperature range. On 20-Jan-2022 the freezer got to 6.1F for 15 minutes, then returned to the appropriate temperature range. On 11-Feb-2022 the freezer got to 10.8F for 10 hours and 15 minutes overnight into 12-Feb-2022, then returned to the appropriate temperature range. On 25-Feb-2022 the freezer got to 22.6F and was out of range for 20 hours total into 26-Feb-2022 then returned to the appropriate temperature range. The storage condition at the time of the excursion was frozen. The vials were moved from freezer to refrigerator on 1 dose/vial on 20-Jan-2022. No visual inspection was done, noting any vaccine state change. No treatment medication reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 24.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 31,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Tested Postive for Covid on May 3, 2022. Had running nose and cough. SLight symptoms have persisted. Retested positive, May 24, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- May 3, 2022, May 24, 2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Coronary Disease
- Andere Medikamente
- Lipitor, Lisingopril, Aspirin, Etymibe
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 63,0
- Geschlecht
- U
- Eingang
- 19.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient administered vaccine on 29-Apr-2022, which was expired on 17-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 29-Apr-2022, which was expired on 17-Apr-2022) in a 63-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 29-Apr-2022, which was expired on 17-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 29-Apr-2022, which was expired on 17-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Patient received the booster dose of Moderna vaccine (Expiry date: 17-Apr-2022). The vial was initially stored in the refrigerator on 29-Apr-2022. Vial did not undergo any temperature excursions. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 86,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
25 doses of expired Moderna COVID-19 vaccine were administered to patients.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna COVID-19 vaccine were administered to patients.) in an 86-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 04-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna COVID-19 vaccine were administered to patients.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna COVID-19 vaccine were administered to patients.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The vial was initially stored in refrigerator on 04-May-2022. The vial didn't undergone any temperature excursion. No treatment medications was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 79,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Expired vaccine was stored in the refrigerator; Expired Moderna COVID-19 vaccine was administered to the patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Moderna COVID-19 vaccine was administered to the patient) and PRODUCT STORAGE ERROR (Expired vaccine was stored in the refrigerator) in a 79-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 04-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Moderna COVID-19 vaccine was administered to the patient). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Expired vaccine was stored in the refrigerator). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired Moderna COVID-19 vaccine was administered to the patient) and PRODUCT STORAGE ERROR (Expired vaccine was stored in the refrigerator) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. The patient received the booster dose. It was reported that the vials were initially stored in the refrigerator was on 29-Apr-2022 and on 04-May-2022. The vial did not undergo any temperature excursions. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 75,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 17-Apr-2022 and on 04-May-2022 moved to refrigeration and was administered on same day; 25 doses of expired Moderna Covid-19 vaccine were administered to patients.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.) and PRODUCT STORAGE ERROR (Vaccine expired on 17-Apr-2022 and on 04-May-2022 moved to refrigeration and was administered on same day) in a 75-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 04-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 17-Apr-2022 and on 04-May-2022 moved to refrigeration and was administered on same day). At the time of the report, EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.) and PRODUCT STORAGE ERROR (Vaccine expired on 17-Apr-2022 and on 04-May-2022 moved to refrigeration and was administered on same day) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vial was initially stored in refrigerator on 04-May-2022. The vial didn't undergone any temperature excursion. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 67,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
25 doses of expired Moderna Covid-19 vaccine were administered to patients.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.) in a 67-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 04-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not provided. Patient received Moderna Covid-19 vaccine as booster dose The vaccine was expired on 17-Apr-2022 .The vial was initially stored in the refrigerator on 29-Apr-2022 and 04-May-2022. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 64,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 17-Apr-2022 and date moved to refrigeration on 29-Apr-2022 and 04-may2022 vaccine was administered; Expired Moderna Covid-19 vaccine was administered to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Moderna Covid-19 vaccine was administered to patient) and PRODUCT STORAGE ERROR (Vaccine expired on 17-Apr-2022 and date moved to refrigeration on 29-Apr-2022 and 04-may2022 vaccine was administered) in a 64-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 04-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Moderna Covid-19 vaccine was administered to patient). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 17-Apr-2022 and date moved to refrigeration on 29-Apr-2022 and 04-may2022 vaccine was administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired Moderna Covid-19 vaccine was administered to patient) and PRODUCT STORAGE ERROR (Vaccine expired on 17-Apr-2022 and date moved to refrigeration on 29-Apr-2022 and 04-may2022 vaccine was administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. The vial was initially stored in the refrigerator on 29-Apr-2022 and 04-May-2022. The vial did not undergo any temperature excursions. No treatment medications was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 65,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.) in a 65-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 04-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. The vial did not undergo any temperature excursions. The vial was initially stored in the refrigerator on 04-May-2022. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 72,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial was initially stored in the refrigerator 29Apr2022 & 04May2022; 25 doses of expired Moderna Covid-19 vaccine were administered to patients.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator 29Apr2022 & 04May2022) in a 72-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 04-May-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator 29Apr2022 & 04May2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator 29Apr2022 & 04May2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product was provided by the reporter. No treatment medication was provided by the reporter. The vial was initially stored in refrigerator on 4may2022. The patient received third full dose. The vial did not undergo any temperature excursion .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 50,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
The vaccine expired on 17-Apr-2022 was administered on 04-May-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vaccine expired on 17-Apr-2022 was administered on 04-May-2022) in a 50-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 04-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vaccine expired on 17-Apr-2022 was administered on 04-May-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vaccine expired on 17-Apr-2022 was administered on 04-May-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications details were not reported by the reporter. The patient received booster dose. The vial did not undergo any temperature excursion. The vial was stored in refrigerator on 04-May-2022. Treatment details was not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 57,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
The vaccine expired on 17-Apr-2022 was administered on 04-May-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vaccine expired on 17-Apr-2022 was administered on 04-May-2022) in a 57-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 04-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vaccine expired on 17-Apr-2022 was administered on 04-May-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vaccine expired on 17-Apr-2022 was administered on 04-May-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The patient received booster dose. Date the vial was initially stored in the refrigerator was on 04-May-2022. The vial did not undergo any temperature excursion. No treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 50,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
The vaccine expired on 17-Apr-2022, was administered on 04-May-2022.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vaccine expired on 17-Apr-2022, was administered on 04-May-2022.) in a 50-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 04-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vaccine expired on 17-Apr-2022, was administered on 04-May-2022.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vaccine expired on 17-Apr-2022, was administered on 04-May-2022.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The patient received booster dose. The vial did not undergo any temperature excursion. The vial was stored in refrigerator on 04-May-2022. No treatment medications was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 79,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial was initially stored in the refrigerator 29Apr2022 & 04May2022; 25 doses of expired Moderna Covid-19 vaccine were administered to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator 29Apr2022 & 04May2022) in a 79-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator 29Apr2022 & 04May2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients) and PRODUCT STORAGE ERROR (Vial was initially stored in the refrigerator 29Apr2022 & 04May2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant drug was reported. The vial was initially stored in the refrigerator on 29-Apr-2022. The vial did not undergo any temperature excursions. The patient received third full dose. No treatment drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 79,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 17-Apr-2022 but was initially stored in the refrigerator on 29-Apr-2022; Patient received the vaccine on 29-Apr-2022, which had expired on 17-Apr-2022.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received the vaccine on 29-Apr-2022, which had expired on 17-Apr-2022.) and PRODUCT STORAGE ERROR (Vaccine expired on 17-Apr-2022 but was initially stored in the refrigerator on 29-Apr-2022) in a 79-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received the vaccine on 29-Apr-2022, which had expired on 17-Apr-2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 17-Apr-2022 but was initially stored in the refrigerator on 29-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received the vaccine on 29-Apr-2022, which had expired on 17-Apr-2022.) and PRODUCT STORAGE ERROR (Vaccine expired on 17-Apr-2022 but was initially stored in the refrigerator on 29-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Vaccine expired on 17-Apr-2022 but was initially stored in the refrigerator on 29-Apr-2022. Concomitant drugs were not reported. Treatment details were not given. The vial did not undergo any temperature excursions
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 67,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
25 doses of expired Moderna Covid-19 vaccine were administered to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patient) in a 67-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patient). At the time of the report, EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patient) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medication were provided. The vial was initially stored in the refrigerator on 29 Apr 2022 and 04 May 2022. The vial does not undergo any temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 64,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
25 doses of expired Moderna Covid-19 vaccine were administered to patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients) in a 64-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients). At the time of the report, EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medications were provided. No treatment medications were provided. It was reported that vial was initially stored in the refrigerator on 29 Apr 2022, 04 May 2022 and did not undergo temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 66,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vaccine expired on 17-Apr-2022 was administered on 29-Apr-2022) in a 66-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vaccine expired on 17-Apr-2022 was administered on 29-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vaccine expired on 17-Apr-2022 was administered on 29-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The patient received booster dose. Date the vial was initially stored in the refrigerator on 29-Apr-2022. The vial did not undergo any temperature excursion. No treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 65,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
25 doses of expired Moderna Covid-19 vaccine were administered to patients.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.) in a 65-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not provided. Patient received Moderna Covid-19 vaccine as booster dose The vial was initially stored in the refrigerator on 29-Apr-2022 and 04-May-2022. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 64,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
25 doses of expired Moderna Covid-19 vaccine were administered to patients.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.) in a 64-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna Covid-19 vaccine were administered to patients.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. Patient received Moderna Covid-19 vaccine as booster dose. The vial was initially stored in the refrigerator on 29 Apr 2022 and 04 May 2022. Vial did not undergo any temperature excursions. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 66,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
25 doses of expired Moderna COVID-19 vaccine were administered to patients.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna COVID-19 vaccine were administered to patients.) in a 66-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna COVID-19 vaccine were administered to patients.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (25 doses of expired Moderna COVID-19 vaccine were administered to patients.) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The vial did not undergo any temperature excursion. The vial was stored in refrigerator on 29-Apr-2022. No treatment medications was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 50,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Date the vial was initially stored in the refrigerator: 29Apr2022 and Date of expiry date 17Apr2022.; Expired Moderna Covid-19 vaccine were administered to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Moderna Covid-19 vaccine were administered to patient) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator: 29Apr2022 and Date of expiry date 17Apr2022.) in a 50-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Moderna Covid-19 vaccine were administered to patient). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator: 29Apr2022 and Date of expiry date 17Apr2022.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired Moderna Covid-19 vaccine were administered to patient) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator: 29Apr2022 and Date of expiry date 17Apr2022.) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported. Date the vial was initially stored in the refrigerator was 29Apr2022 & 04May2022. The vial did not undergone any temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 59,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired Moderna Covid-19 vaccine was administered; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Moderna Covid-19 vaccine was administered) in a 59-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Moderna Covid-19 vaccine was administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired Moderna Covid-19 vaccine was administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Patient received the booster dose of Moderna vaccine (Expiry date: 17-Apr-2022). The vial was initially stored in the refrigerator on 29-Apr-2022. Vial did not undergo any temperature excursions. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 33,0
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 29.04.2022
- Beginn
- 29.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 17-Apr-2022 but was initially stored in the refrigerator and administered on 29-Apr-2022; dose of expired Moderna Covid-19 vaccine was administered to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (dose of expired Moderna Covid-19 vaccine was administered to patient) and PRODUCT STORAGE ERROR (Vaccine expired on 17-Apr-2022 but was initially stored in the refrigerator and administered on 29-Apr-2022) in a 33-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 29-Apr-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 29-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (dose of expired Moderna Covid-19 vaccine was administered to patient). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 17-Apr-2022 but was initially stored in the refrigerator and administered on 29-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (dose of expired Moderna Covid-19 vaccine was administered to patient) and PRODUCT STORAGE ERROR (Vaccine expired on 17-Apr-2022 but was initially stored in the refrigerator and administered on 29-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. The vial was initially stored in refrigerator on 29-Apr-2022. The vial did not undergo any temperature excursions. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.05.2022
- Impfdatum
- 03.05.2022
- Beginn
- 03.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Received Expired Vaccine beyond the manufacturer's expiration date; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received Expired Vaccine beyond the manufacturer's expiration date) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 03-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 03-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received Expired Vaccine beyond the manufacturer's expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received Expired Vaccine beyond the manufacturer's expiration date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications information was not reported. Vial did not undergo any temperature excursions. The vial was initially stored in the refrigerator on 13 APR 2022. No treatment medications were provided. Most recent FOLLOW-UP information incorporated above includes: On 12-May-2022: Live follow-up added: Reporter added, initial reporter address, the date of vial was initially stored in the refrigerator was updated
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.05.2022
- Impfdatum
- 10.05.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Received Expired Vaccine beyond the manufacturer's expiration date-3rd patient 10MAY2022/Two patients each received expired Moderna Covid-19 vaccine; This spontaneous case was reported by a physician assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received Expired Vaccine beyond the manufacturer's expiration date-3rd patient 10MAY2022/Two patients each received expired Moderna Covid-19 vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 10-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 10-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received Expired Vaccine beyond the manufacturer's expiration date-3rd patient 10MAY2022/Two patients each received expired Moderna Covid-19 vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received Expired Vaccine beyond the manufacturer's expiration date-3rd patient 10MAY2022/Two patients each received expired Moderna Covid-19 vaccine) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Reporter stated that two patients received Moderna Covid-19 vaccine which was expired. Date the vial was initially stored in the refrigerator was 13-APR-2022. The vial did not undergo any temperature excursions. No treatment medication was reported. Most recent FOLLOW-UP information incorporated above includes: On 12-May-2022: Live Followup included primary and secondary reporter details and the date of vial was initially stored in the refrigerator was updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- 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
Received Vaccine that expired on 4-17-2022, information from Moderna internal analysis: Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Recieved vaccine that expired on 4-17-2022, from Moderna internal communications: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknownf
- Allergien
- unknownf
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 96,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- Unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine Received expired on 4-17-22, reported to Moderna, information from internal audit "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- uknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine received Expired on 4-17-22, report to Moderna, findings from internal review of vaccine: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was stored in refrigerator on 01 Apr 2022 and was expired on 17 Apr 2022 and administered on 20 Apr 2022; Expired vaccine that expired on 17April2022 and they think it was administer to 6 people; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine that expired on 17April2022 and they think it was administer to 6 people) and PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 01 Apr 2022 and was expired on 17 Apr 2022 and administered on 20 Apr 2022) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine that expired on 17April2022 and they think it was administer to 6 people). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 01 Apr 2022 and was expired on 17 Apr 2022 and administered on 20 Apr 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine that expired on 17April2022 and they think it was administer to 6 people) and PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 01 Apr 2022 and was expired on 17 Apr 2022 and administered on 20 Apr 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was provided. Vial did not undergo any temperature excursions. No treatment medications was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 30.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
This spontaneous case reported by a nurse, describes the occurrence of administered expired product (vaccine expired April 17, 2022, believed to be administered to 6 people) and product storage error (vaccine stored past expiry date) in a 29-year-old male patient who received mRNA-1273 (Moderna COVID-19 vaccine, batch/lot# 016J212A) for COVID-19 immunization. No medical history reported. On Apr 20, 2022, patient received the second dose of mRNA-1273 (Moderna COVID-19 vaccine), unknown route; 1 dosage form. On Apr 20, 2022, patient administered expired product (vaccine expired April 17, 2022, believed to be administered to 6 people). On an unknown date, patient experienced product storage error (vaccine stored past expiry date). At the time of the report, administered expired product (vaccine expired April 17, 2022, believed to be administered to 6 people) and product storage error (vaccine stored past expiry date) outcome: unknown. The reporter did not provide any causality assessments, concomitant medication or treatment information. The vial did not undergo any temperature excursions. Vial initially stored in the refrigerator on April 1, 2022. This case linked to MOD-2022-545248 (patient link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 30.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
This spontaneous case reported by a nurse, describes the occurrence of administered expired product (vaccine expired on April 17, 2022; given to patient) and product storage error (vaccine stored in refrigerator on Apr 1, 2022, expired on Apr 17, 2022 and administered on Apr 20, 2022) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 vaccine, batch/lot# 016J212A) for COVID-19 immunization. No medical history reported. On Apr 20, 2022, patient received a dose of mRNA-1273 (Moderna COVID-19 vaccine), unknown route; 1 dosage form. On Apr 20, 2022, patient administered expired product (vaccine expired on April 17, 2022; given to patient). On an unknown date, patient experienced product storage error (vaccine stored in refrigerator on Apr 1, 2022, expired on Apr 17, 2022 and administered on Apr 20, 2022). At the time of the report, administered expired product (vaccine expired on April 17, 2022; given to patient) and product storage error (vaccine stored in refrigerator on Apr 1, 2022, expired on Apr 17, 2022 and administered on Apr 20, 2022) outcome: unknown. The reporter did not provide any causality assessments, concomitant medication or treatment information. The patient received 2nd booster. The vial initially stored in the refrigerator on April 1, 2022. Vial did not undergo with any temperature excursions. This case linked to MOD-2022-545248 (patient link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 30.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
This spontaneous case reported by a nurse, describes the occurrence of administered expired product (expired vaccine given to patient) and product storage error (vial initially stored in the refrigerator on April 1, 2022; administered April 20, 2022) in a 73-year-old male patient who received mRNA-1273 (Moderna COVID-19 vaccine, batch/lot# 016J212A) for COVID-19 immunization. No medical history reported. On Apr 20, 2022, patient received the fourth dose of mRNA-1273 (Moderna COVID-19 vaccine), unknown route; 1 dosage form. On Apr 20, 2022, patient administered expired product (expired vaccine given to patient). On an unknown date, patient experienced product storage error (vial initially stored in the refrigerator on April 1, 2022; administered April 20, 2022). At the time of the report, administered expired product (expired vaccine given to patient) and product storage error (vial initially stored in the refrigerator on April 1, 2022; administered April 20, 2022) outcome: unknown. The reporter did not provide any causality assessments, concomitant medication or treatment information. On April 1, 2022, vial was initially stored in the refrigerator. Vial did not undergo any temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 30.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial expired on 17-Apr-2022, stored in refrigerator on 18-Apr-2022 and administered on 19-Apr-2022.; patient was administered an expired dose of the vaccine for the booster; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient was administered an expired dose of the vaccine for the booster) and PRODUCT STORAGE ERROR (Vial expired on 17-Apr-2022, stored in refrigerator on 18-Apr-2022 and administered on 19-Apr-2022.) in a 64-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No medical history was provided by the reporter. Concomitant products included CARVEDILOL, VARENICLINE and VITAMIN C [ASCORBIC ACID] for an unknown indication. On 19-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 19-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient was administered an expired dose of the vaccine for the booster). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial expired on 17-Apr-2022, stored in refrigerator on 18-Apr-2022 and administered on 19-Apr-2022.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient was administered an expired dose of the vaccine for the booster) and PRODUCT STORAGE ERROR (Vial expired on 17-Apr-2022, stored in refrigerator on 18-Apr-2022 and administered on 19-Apr-2022.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. It was reported that patient received 1st booster dose. Treatment medications were not provided. It was reported that the vial was stored in refrigerator after expiry on 18-Apr-2022. The vial did not undergo any temperature excursion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- CARVEDILOL; VARENICLINE; VITAMIN C [ASCORBIC ACID]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 30.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Date the vial was initially stored in the refrigerator on 01-April-2022 and administered on 20-April-2022; Expired vaccine given to 6 patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine given to 6 patients) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator on 01-April-2022 and administered on 20-April-2022) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine given to 6 patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator on 01-April-2022 and administered on 20-April-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine given to 6 patients) and PRODUCT STORAGE ERROR (Date the vial was initially stored in the refrigerator on 01-April-2022 and administered on 20-April-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Patient received second booster dose. The vial initially stored in the refrigerator on 01-Apr-2022. The vaccine expired on17-April-2022. The vial did not undergo any temperature excursions. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 30.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was stored in refrigerator on 01 Apr 2022 and was expired on 17 Apr 2022 and administered on 20 Apr 2022; Vaccine was stored in refrigerator on 01 Apr 2022 and was expired on 17 Apr 2022 and administered on 20 Apr 2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was stored in refrigerator on 01 Apr 2022 and was expired on 17 Apr 2022 and administered on 20 Apr 2022) and PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 01 Apr 2022 and was expired on 17 Apr 2022 and administered on 20 Apr 2022) in an 83-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016j21-2a) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was stored in refrigerator on 01 Apr 2022 and was expired on 17 Apr 2022 and administered on 20 Apr 2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 01 Apr 2022 and was expired on 17 Apr 2022 and administered on 20 Apr 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was stored in refrigerator on 01 Apr 2022 and was expired on 17 Apr 2022 and administered on 20 Apr 2022) and PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 01 Apr 2022 and was expired on 17 Apr 2022 and administered on 20 Apr 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not reported. Patient received second booster dose. Date of refrigeration was 01-Apr-2022. It was reported that vial had not undergone any temperature excursions. Treatment medication was not reported. Most recent FOLLOW-UP information incorporated above includes: On 20-Apr-2022: Non-significant Follow-up appended- I narrative updated. On 25-Apr-2022: Follow-up ? No New Information received On 27-Apr-2022: Follow up received contains reporters details and I narrative with information regarding the 6 patient was updated. On 27-Apr-2022: Report type changed from invalid to spontaneous. Added patient demographics and suspect product dose number. Updated I narrative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 4-17-22, reported to Moderna, results from internal testing: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 4-17-22, reported to Moderna, internal testing done and this was the result: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine expired on 4-17-22, reported to Moderna, internal testing done and this was the result: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine expired on 4-17-22, reported to Moderna, internal testing done and this was the result: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 4-17-22, reported to Moderna, internal testing done and this was the result: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 4-17-22, reported to Moderna, internal testing done and this was the result: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine expired on 4-17-22, reported to Moderna, internal testing done and this was the result: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine expired on 4-17-22, reported to Moderna, internal testing done and this was the result: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine expired on 4-17-22, reported to Moderna, internal testing done and this was the result: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vaccine expired on 4-17-22, reported to Moderna, internal testing done and this was the result: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine expired on 4-17-22, reported to Moderna, internal testing done and this was the result: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- Unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 4-17-22, reported to Moderna, internal testing done and this was the result: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 28.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- 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
Symptomtext
Vaccine expired on 4-17-22, reported to Moderna, internal testing done and this was the result: "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Received expired vaccine, vaccine expired on 4-17-22, Moderna contacted, and this was the report "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
Received expired vaccine, vaccine expired on 4-17-22, Moderna contacted, and this was the report "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 28.04.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Received expired vaccine, Moderna contacted, and this was the report "Analysis of the vials associated with your storage excursion is complete. The vaccine administered on April 19, 20, 21, 2022 from lot number 016J21-2A maintained the activity necessary to protect against the SARS-CoV-2 (COVID-19) virus at time of administration."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unkown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 21.01.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Flushing
Hot flush
Hyperhidrosis
Nasal congestion
Nasopharyngitis
Rhinorrhoea
SARS-CoV-2 test
Sneezing
Tinnitus
Vision blurred
Visual impairment
Symptomtext
Stuffy nose, blurry vision, ringing in my ears. It was mainly like cold symptoms. I had sneezing and running nose. I still have those issues. I'm not sure if its allergy related or not. Every now and then I become flushed and you sweat a lot. It's like having a hot flash. The ringing in the ears and blurry vision is on and off. It happens every once in a while.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Flushing
- Hospital-Tage
- -
- Labordaten
- COVID-19 test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Lisinopril
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 26.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was placed in refrigerator on 23-Mar-2022, Beyond use date on 17-Apr-2022 administration date on 19-Apr-2022; Past beyond use date Moderna Covid-19 vaccine given to 6 patients.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Past beyond use date Moderna Covid-19 vaccine given to 6 patients.) and PRODUCT STORAGE ERROR (Vaccine was placed in refrigerator on 23-Mar-2022, Beyond use date on 17-Apr-2022 administration date on 19-Apr-2022) in a male patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 19-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 19-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Past beyond use date Moderna Covid-19 vaccine given to 6 patients.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was placed in refrigerator on 23-Mar-2022, Beyond use date on 17-Apr-2022 administration date on 19-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Past beyond use date Moderna Covid-19 vaccine given to 6 patients.) and PRODUCT STORAGE ERROR (Vaccine was placed in refrigerator on 23-Mar-2022, Beyond use date on 17-Apr-2022 administration date on 19-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Date the vial was initially stored in the refrigerator on 23 Mar 2022. Beyond use date was on 17 Apr 2022. The vial did not undergo any temperature excursions. The treatment information was unknown. This case was linked to MOD-2022-546561, MOD-2022-546566, MOD-2022-546544, MOD-2022-546563, MOD-2022-546559 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 22-Apr-2022: Follow-up received contains Significant information date of administration of vaccine was updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was stored past its use beyond date.; past beyond use date Moderna Covid-19 vaccine given to 6 patients.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (past beyond use date Moderna Covid-19 vaccine given to 6 patients.) and PRODUCT STORAGE ERROR (Vaccine was stored past its use beyond date.) in a female patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 19-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 19-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (past beyond use date Moderna Covid-19 vaccine given to 6 patients.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was stored past its use beyond date.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (past beyond use date Moderna Covid-19 vaccine given to 6 patients.) and PRODUCT STORAGE ERROR (Vaccine was stored past its use beyond date.) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. Vial was initially stored in the refrigerator on 23 March 2022 and the vial didn't undergo any temperature excursions. It was reported that dose administered after 30-day use By date or after manufacturer date of expiry and beyond use date was 17-APR-2022. No treatment medication information was provided. This case was linked to MOD-2022-546563, MOD-2022-546566, MOD-2022-546561, MOD-2022-546544 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 22-Apr-2022: Follow-up received included date of administration of expired vaccine and event onset date updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired Moderna Covid-19 vaccine given to 6 patients/beyond use date is 17APR2022 and administration date 20 Apr 2022; This spontaneous case was reported by a health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Moderna Covid-19 vaccine given to 6 patients/beyond use date is 17APR2022 and administration date 20 Apr 2022) in a female patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 20-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Moderna Covid-19 vaccine given to 6 patients/beyond use date is 17APR2022 and administration date 20 Apr 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired Moderna Covid-19 vaccine given to 6 patients/beyond use date is 17APR2022 and administration date 20 Apr 2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were mentioned. No treatment details were reported. The vaccine vial was initially stored in the refrigerator on 23-Mar-2022 and was administered on 20-Apr-2022. The vial did not undergo any temperature excursions. The vaccine was given to 3 Males and 3 Females. Patient's age was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 25.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine beyond use date 17APR2022; Past beyond use date Moderna Covid-19 vaccine given to 6 patients.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Past beyond use date Moderna Covid-19 vaccine given to 6 patients.) and PRODUCT STORAGE ERROR (Vaccine beyond use date 17APR2022) in a male patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 20-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Past beyond use date Moderna Covid-19 vaccine given to 6 patients.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine beyond use date 17APR2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Past beyond use date Moderna Covid-19 vaccine given to 6 patients.) and PRODUCT STORAGE ERROR (Vaccine beyond use date 17APR2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Vial was initially stored in the refrigerator on 23-MAR-2022. Vial did not undergo any temperature excursion. No relevant concomitant medications were reported. No treatment information was provided. This case was linked to MOD-2022-546559, MOD-2022-546563, MOD-2022-546567, MOD-2022-546561 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- M
- Eingang
- 25.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vial was initially stored in refrigerator on 23 Mar 2022, beyong use date was 17 Apr 2022 and administered on 20 Apr 2022.; past beyond use date Moderna Covid-19 vaccine given to 6 patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (past beyond use date Moderna Covid-19 vaccine given to 6 patients) and PRODUCT STORAGE ERROR (The vial was initially stored in refrigerator on 23 Mar 2022, beyong use date was 17 Apr 2022 and administered on 20 Apr 2022.) in a male patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 20-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (past beyond use date Moderna Covid-19 vaccine given to 6 patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in refrigerator on 23 Mar 2022, beyong use date was 17 Apr 2022 and administered on 20 Apr 2022.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (past beyond use date Moderna Covid-19 vaccine given to 6 patients) and PRODUCT STORAGE ERROR (The vial was initially stored in refrigerator on 23 Mar 2022, beyong use date was 17 Apr 2022 and administered on 20 Apr 2022.) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. The vial was initially stored in the refrigerator on 23-Mar-2022. The vial did not undergo any temperature excursions. The vaccine's beyond use date was reported as 17-Apr-2022. No treatment medications were provided. This case was linked to MOD-2022-546559, MOD-2022-546567, MOD-2022-546561, MOD-2022-546566, MOD-2022-546544 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial initially stored in refrigerator on 23 Mar 2022, Vaccine beyond use date 17APR2022, Administration date was 20 Apr 2022; Past beyond use date Moderna Covid-19 vaccine given to 6 patients.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Past beyond use date Moderna Covid-19 vaccine given to 6 patients.) and PRODUCT STORAGE ERROR (Vial initially stored in refrigerator on 23 Mar 2022, Vaccine beyond use date 17APR2022, Administration date was 20 Apr 2022) in a female patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 20-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Past beyond use date Moderna Covid-19 vaccine given to 6 patients.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial initially stored in refrigerator on 23 Mar 2022, Vaccine beyond use date 17APR2022, Administration date was 20 Apr 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Past beyond use date Moderna Covid-19 vaccine given to 6 patients.) and PRODUCT STORAGE ERROR (Vial initially stored in refrigerator on 23 Mar 2022, Vaccine beyond use date 17APR2022, Administration date was 20 Apr 2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. Vial was initially stored in the refrigerator on 23 Mar 2022. The beyond use date was 17 Apr 2022. Vial did not undergo any temperature excursion. No treatment information was provided. This case was linked to MOD-2022-546559, MOD-2022-546563, MOD-2022-546567, MOD-2022-546561, MOD-2022-546566, MOD-2022-546561 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the Beyond Use Date of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the Beyond Use Date of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the Beyond Use Date of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Moderna was administered after the Beyond Use Date of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 03.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Moderna was administered after the BUD of 3/30/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 03.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 03.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 03.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 03.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the BUD of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Moderna was administered after the Beyond use date of 3/30/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 04.04.2022
- Impfdatum
- 01.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Tinnitus in both left and right ears starting shortly after booster vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 04.04.2022
- Impfdatum
- 01.03.2022
- Beginn
- 03.03.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Parosmia
Symptomtext
Sense of smell changed, onions, feces, bad breath, gasoline; all smell to me like antifreeze
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Parosmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- Asthma, gerd
- Andere Medikamente
- None
- Allergien
- Mucunex, dogs, cats,horses, hay, cockroaches, bees, polin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 30.03.2022
- Impfdatum
- 27.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram
Heart rate increased
Symptomtext
High heart rate (130s-140s)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electrocardiogram
- Hospital-Tage
- -
- Labordaten
- EKG
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Prenatal vitamins, cetirizine, and vitamin d3 2000 IU
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 29.03.2022
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Symptomtext
Patient was incorrectly administered a second booster following the completion of the primary series and approved booster. Vaccination was given approximately 5 months after booster dose. No adverse symptoms have been observed at this point.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Neomycin, Tetracycline
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
The patient believed to be 18 by the person who administered the vaccination; therefore a Moderna dose given at the request of the patient and patient's parent. It was discovered immediately after administration the patient will not be 18 until May.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 09.03.2022
- Impfdatum
- 01.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
Administered wrong COVID19 booster to pt. Provider ordered Pfizer booster and pt was given moderna booster instead. Writer did not verify the order prior to administration because the pharmacist was in the pt chart at the same time. When documenting the administration, writer realized the error and reported to RN and Dr. Dr. instructed RN to notify patient who was still in the room. Patient had no other concerns.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
12 year old patient received a dose of the Moderna COVID-19 vaccine on 2 separate dates as dose 1 and dose 2 in their vaccination series. No adverse events have been documented as a result of the administrations to date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022; Received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022) in a 32-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 18-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The healthcare professional (HCP) wanted to know whether the patient should revaccinate or not. The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022. The vials did not undergo any temperature excursions. No treatment medications were reported. This case was linked to MOD-2022-500959 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022; Patients received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022) in a 21-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 18-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that the vial had not undergone any temperature excursions. No treatment medications were reported. This case was linked to MOD-2022-500959 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022; Patient received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022) and EXPIRED PRODUCT ADMINISTERED (Patient received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 18-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022). At the time of the report, PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022) and EXPIRED PRODUCT ADMINISTERED (Patient received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported. The vial was initially stored in the refrigerator on 10-Jan-2022 and administered on 18-Feb-2022. It was reported that the vial had not undergone any temperature excursions. This case was linked to MOD-2022-500959 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 18.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date; Received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date) and PRODUCT STORAGE ERROR (Received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date) in a 46-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 18-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In February 2022, the patient experienced PRODUCT STORAGE ERROR (Received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date). On 18-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date) and PRODUCT STORAGE ERROR (Received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day use-by-date) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The healthcare professional (HCP) wanted to know whether the patient should revaccinate or not. The vial was initially stored in the refrigerator on 10-Jan-2022. The vials did not undergo any temperature excursions. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 18.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Patients received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day; vial initially stored in the refrigerator was 10-Jan-2022 but patients received vaccine 10 days after the 30-day; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day) and PRODUCT STORAGE ERROR (vial initially stored in the refrigerator was 10-Jan-2022 but patients received vaccine 10 days after the 30-day) in an 88-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 18-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In February 2022, the patient experienced PRODUCT STORAGE ERROR (vial initially stored in the refrigerator was 10-Jan-2022 but patients received vaccine 10 days after the 30-day). On 18-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients received a booster dose of the Moderna COVID19 vaccine 10 days after the 30-day) and PRODUCT STORAGE ERROR (vial initially stored in the refrigerator was 10-Jan-2022 but patients received vaccine 10 days after the 30-day) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medications were reported It was reported that the vial did not undergo any temperature excursions. It was reported that there was a correction only 1 bottle of Moderna Lot Number 016J21-2A that was opened and administered on 18-Feb-2022 to 5 people. No Treatments were reported. This case was linked to MOD-2022-501758, MOD-2022-501759 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 03-Mar-2022: Follow up information received, case updated to spontaneous from invalid, patient information added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Muscle spasms
Symptomtext
Patient is complaining of spasms in her back, claims to have had no symptoms after 1st 2 vaccinations but experienced the spasms after her booster dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Muscle spasms
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- rosuvastatin 10mg, Risperdal 1mg, Bupropion SR 150mg, Clindamycin 1% lotion
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Head titubation
Lymphadenopathy
Symptomtext
tremor started on her head, with no motion from left to right; she felt cranky; extreme swelling of the lymph nodes on her right arm and armpit after the injection; This spontaneous case was reported by a consumer and describes the occurrence of HEAD TITUBATION (tremor started on her head, with no motion from left to right), FEELING ABNORMAL (she felt cranky) and LYMPHADENOPATHY (extreme swelling of the lymph nodes on her right arm and armpit after the injection) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. The patient's past medical history included Cancer (There was no recent change in status (such as improvement or worsening)) from 2016 to 2017. Previously administered products included for Drug use for unknown indication: chicken pox vaccine (The patient received chicken pox vaccine around both first 2 doses of COVID-19 vaccine). Past adverse reactions to the above products included No adverse event with chicken pox vaccine. Concurrent medical conditions included Neck discomfort (Start date: 25 years ago and there was no recent change in status (such as improvement or worsening)), Arthritis (Start date: 15 years ago and there was no recent change in status (such as improvement or worsening)) and Scoliosis (Start date: since the patient was born and there was no recent change in status (such as improvement or worsening)). Concomitant products included IBUPROFEN for Neck discomfort, ACYCLOVIR [ACICLOVIR] and VITAMINS NOS for an unknown indication. On 31-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 31-Jan-2022, the patient experienced FEELING ABNORMAL (she felt cranky) and LYMPHADENOPATHY (extreme swelling of the lymph nodes on her right arm and armpit after the injection). On 01-Feb-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced HEAD TITUBATION (tremor started on her head, with no motion from left to right). On 03-Feb-2022, FEELING ABNORMAL (she felt cranky) and LYMPHADENOPATHY (extreme swelling of the lymph nodes on her right arm and armpit after the injection) had resolved. At the time of the report, HEAD TITUBATION (tremor started on her head, with no motion from left to right) had not resolved. The extreme swelling of the lymph nodes was lasted for 2 to 3 days. The patient thought that the tremor might be related to previous neck issues. The patient visited to her doctor because of tremor and no treatment was given, but doctor told her that they would watch the symptom for a while. The tremor was still ongoing and worsened as well. Treatment information for the events feeling abnormal and swollen lymph nodes were not reported by the reporter. This case was linked to MOD-2022-495240, MOD-2022-495173 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling abnormal
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Arthritis (Start date: 15 years ago and there was no recent change in status (such as improvement or worsening)); Neck discomfort (Start date: 25 years ago and there was no recent change in status (such as improvement or worsening)); Scoliosis (Start date: since the patient was born and there was no recent change in status (such as improvement or worsening))
- Vorgeschichte
- Medical History/Concurrent Conditions: Cancer (There was no recent change in status (such as improvement or worsening))
- Andere Medikamente
- ACYCLOVIR [ACICLOVIR]; IBUPROFEN; VITAMINS NOS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 25.02.2022
- Impfdatum
- 27.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Patient is outside of the vaccine age recommendation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 24.02.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
No adverse event
Symptomtext
No adverse event. Patient given Moderna booster outside of recommended guidelines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 21.02.2022
- Impfdatum
- 15.01.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Accidental underdose
Symptomtext
booster given instead of second dose; This spontaneous case was reported by a nurse and describes the occurrence of ACCIDENTAL UNDERDOSE (booster given instead of second dose) in a 57-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 045L21A and 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 15-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Feb-2022, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to .25 milliliter. On 12-Feb-2022, the patient experienced ACCIDENTAL UNDERDOSE (booster given instead of second dose). On 12-Feb-2022, ACCIDENTAL UNDERDOSE (booster given instead of second dose) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Booster vaccine given two months early.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Full blood count
Joint range of motion decreased
Laboratory test normal
Periarthritis
Platelet count decreased
Sensory disturbance
Skin discolouration
Symptomtext
I went in to get my CBC done just because the last times I got my vaccines, my platelet counts really dropped. It?s like a protocol now to go before, after, and monitor for 6 weeks. Since I have ITT, I already have low platelet count anyway. Got my CBC done yesterday and the platelet count was at 68,000 on Monday and it was at 30,000 yesterday after the vaccine. Now I will just be monitoring to see that it goes back up. Still ongoing since 2nd vaccination and still being treated for the following: Bottoms of feet turn purple. Every test done and nothing in relation to circulation. Tests cannot determine the problem. There's just this sensation and I check my feet and they're purple. Noted with dermatologist. Thought that it would go away and it's been since the 2nd vaccine and that was back in April 2021. Around the same time where I began having shoulder issues. Seems to be frozen shoulder. Was going to PT and that never helped. Finally got a steroid injection in January 2022, but I still have limited mobility and going to PT again. They said it should be another year or so until I get some mobility.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Full blood count
- Hospital-Tage
- -
- Labordaten
- CBC Panel 02/17/2022- Indicated 30,000 platelet count Tests for foot, circulation, etc. - nothing indicated
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- SLE, ITT
- Andere Medikamente
- Mycophenolate sodium Multivitamin Calcium Vitamin D3 Probiotic Hydroxychloroquine
- Allergien
- Shellfish Plankton
- Vorherige Impfungen
- All previous Moderna COVID vaccines- platelet counts have dropped significantly after vaccines.
- Staat
- -
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered after vial being punctured and left at room temperature for almost 23 hours) in a 22-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 14-Feb-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered after vial being punctured and left at room temperature for almost 23 hours). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered after vial being punctured and left at room temperature for almost 23 hours) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided by the reporter. It was reported that the vial was initially stored in refrigerator on 28-Jan-2022 and the vial was first punctured on 13-Feb-2022 at 11:11 AM. The vial was punctured and then left at room temperature range (8 Degree Celsius to 25 Degree Celsius) for about 23 hours. Patient was administered with the vaccine on 14-Feb-2022. The vial did not undergo any temperature excursions. Reporter stated that they gave the patient two doses at their facility but was not sure if this is their booster or second dose. No treatment medication was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 16.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient was given the wrong vaccine since he is under the age of 18.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None known.
- Vorgeschichte
- Leukocytopenia, Down's syndrome, Expressive speech
- Andere Medikamente
- Brevoxyl, Zyrtec, Metrogel, Elocon
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- 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
Administered booster dose of Moderna twenty two days early from second dose as a result of mistaking the second dose written date as 8/30/2021 instead 9/30/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- None reported
- Andere Medikamente
- Unknown
- Allergien
- ASA and Codeine
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 29.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
On Saturday, January 29, 2022, the patient presented to the clinic to receive a Moderna vaccine. She told administrative assistant "I'm here for my booster vaccine". The administrative assistant retrieved the patient's vaccination record where she saw the patient's 1st dose logged. The administrative assistant applied a green sticker - which we use indicating a Moderna Booster dose - to the recipient's intake form and wrote a "2" on the sticker. The administrative assistant also applied a green sticker to the patient's vaccination card indicating she was receiving her booster dose even though the recipient never received a 2nd dose of Moderna. Register nurse (RN)vaccinated the patient with a booster dose of Moderna 0.25 ml. Later, the RN realized that the patient should have received a 2nd full dose and that she gave the recipient the booster dose - half of the recommended dose of 0.5 mL Moderna. Observation staff caught the error and brought it to the attention of the draw team lead. Usual practice is that vaccinators present the intake form with the sticker indicating the desired vaccine and dose to the draw team which distributes the appropriate vaccine syringe to the vaccine applicator. Regional Lead was notified. He phoned and spoke with the patient at about 3:30 pm inviting her to return to receive the remainder of her vaccine regimen and told her that our clinic would close at 6 pm. The patient did not return that day. The regional lead again attempted to contact and left a voicemail with the patient's phone on Tuesday, Feb 1st, 2022, which was the next day the clinic was open. As of today, February 9th, the patient still has not returned to the clinic for the additional half-dose and the registry does not indicate she has received the remainder elsewhere. The incident was reviewed with above staff. Today, February 9th, the patient's account in the Registry still incorrectly states that she received the 0.5 mL dose of Moderna instead of 0.25 mL. Assistant Site Lead.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 09.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
product storage error; Patient were given dose of the Moderna COVID 19 after 30-day Use By Date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient were given dose of the Moderna COVID 19 after 30-day Use By Date) and PRODUCT STORAGE ERROR (product storage error) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 07-Feb-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient were given dose of the Moderna COVID 19 after 30-day Use By Date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (product storage error). On 07-Feb-2022, EXPIRED PRODUCT ADMINISTERED (Patient were given dose of the Moderna COVID 19 after 30-day Use By Date) had resolved. At the time of the report, PRODUCT STORAGE ERROR (product storage error) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Treatment medication was not provided. Concomitant medication was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 01.01.2022
- Beginn
- 01.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Contusion
Symptomtext
Bruising on his arm to the elbow a few days after the booster shot was administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Contusion
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Had Covid
- Vorgeschichte
- Only has one kidney
- Andere Medikamente
- Warfarin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 29.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient received second dose of primary series at day 21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none
- Andere Medikamente
- none listed
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Gave a pediatric patient a 0.25mL dose of Moderna. No adverse effects as of now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
expired Moderna COVID-19 booster dose administered greater than 12 hours post puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired Moderna COVID-19 booster dose administered greater than 12 hours post puncture) in a 35-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 25-Jan-2022 at 10:05 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 25-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired Moderna COVID-19 booster dose administered greater than 12 hours post puncture). On 25-Jan-2022, EXPIRED PRODUCT ADMINISTERED (expired Moderna COVID-19 booster dose administered greater than 12 hours post puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant and treatment medications were reported. Date the vial initially stored in the refrigerator was 21 Jan 2022 at 7:00 AM. Date and time vial was first punctured was 24 Jan 2022 at 8:45 AM vial didn't undergo any temperature excursions. Total amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) 25 hours. The vial was stored post puncture at room temperature.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (3 Doses administered more than 12(US) hours post puncture) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. The patient's past medical history included Pain. Concomitant products included IBUPROFEN for Pain, ALPRAZOLAM, ASPIRIN [ACETYLSALICYLIC ACID], COLECALCIFEROL (VIT D3), GABAPENTIN, LAMOTRIGINE, METHYLPHENIDATE, MYCOPHENOLATE MOFETIL (MYCOPHENOLATE) and NAPROXEN for an unknown indication. On 20-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 20-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (3 Doses administered more than 12(US) hours post puncture). On 20-Jan-2022, EXPIRED PRODUCT ADMINISTERED (3 Doses administered more than 12(US) hours post puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No treatment medication were provided. This case was linked to MOD-2022-458512, MOD-2022-458470 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Pain
- Andere Medikamente
- Alprazolam; Aspirin [Acetylsalicylic Acid]; Vitamin D3; Gabapentin; Ibuprofen; Lamotrigine; Methylphenidate; Mycophenolate; Naproxen
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Patient requested Pfizer and was given Moderna. Records updated to show correct vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- 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
Patient was given their booster in 2.5 months instead of 5 months. Patient didn't have any kind of adverse reaction while at the pharmacy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Blood thinner, spironolactone
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Postmenopausal haemorrhage
Symptomtext
Patient has been post-menapausal for 3 years. One day after receiving the Moderna COVID vaccine, she started menstrual bleeding which lasted about 24 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Postmenopausal haemorrhage
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- menapausal for 3 years
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
No adverse event
Symptomtext
Patient given moderna booster (0.25 dose) after having Pfizer adult vaccine 8/20/2022. No adverse symptoms/reactions currently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- PTSD, Major depressive disorder, Schizophrenia, schizoaffective disorder, seizure disorder
- Andere Medikamente
- divalproex 500mg, tegratol 200mg
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental underdose
Incorrect route of product administration
Vaccination site discharge
Vaccination site erythema
Vaccination site warmth
Symptomtext
Hot to touch; Likely less than full dose injected; Leaked onto skin; Not injected into muscle; Red patch; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE WARMTH (Hot to touch), ACCIDENTAL UNDERDOSE (Likely less than full dose injected), VACCINATION SITE DISCHARGE (Leaked onto skin), INCORRECT ROUTE OF PRODUCT ADMINISTRATION (Not injected into muscle) and VACCINATION SITE ERYTHEMA (Red patch) in a 40-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 18-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Jan-2022, the patient experienced VACCINATION SITE WARMTH (Hot to touch), ACCIDENTAL UNDERDOSE (Likely less than full dose injected), VACCINATION SITE DISCHARGE (Leaked onto skin), INCORRECT ROUTE OF PRODUCT ADMINISTRATION (Not injected into muscle) and VACCINATION SITE ERYTHEMA (Red patch). On 18-Jan-2022, ACCIDENTAL UNDERDOSE (Likely less than full dose injected), VACCINATION SITE DISCHARGE (Leaked onto skin) and INCORRECT ROUTE OF PRODUCT ADMINISTRATION (Not injected into muscle) had resolved. At the time of the report, VACCINATION SITE WARMTH (Hot to touch) had not resolved and VACCINATION SITE ERYTHEMA (Red patch) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient reported that ice pad application helped little. Concomitant information was not reported. Treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure fluctuation
Bradycardia
Symptomtext
Patient received MOD #3 (ADD/Immuno Dose) IMZ on 01/22/2022 at 03:33 PM. Patient called on 01/23/2022 at 12:30 PM indicating fluctuating blood pressure and bradycardia. Patient indicates one reading of 148/58 with 42 BPM. Patient indicates another reading of 157/73 with 43 BPM. Patient indicates other heart rate reading ranging from 38 to 44 BPM. Recommended patient go to the emergency room for evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood pressure fluctuation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension Crohn's
- Andere Medikamente
- Lisinopril Furosemide Metoprolol ER Entyvio
- Allergien
- -
- Vorherige Impfungen
- "COVID ARM" after MODerna Dose #2 (03/22/2021)
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Conjunctival haemorrhage
Influenza like illness
Lymphadenopathy
Ophthalmological examination
Symptomtext
In addition to swollen lymph nodes in left armpit and flu-like symptoms, I also experienced bilateral Subconjunctival hemorrhage. Approximately 3 days after my injection, I looked in the mirror and noticed that the blood vessels had burst on the outside of both of my eyes. It kept looking worse, even as my other side-effects improved. I went to an optometrist and had to pay out of pocket because my insurance doesn't cover it. I don't wear eye glasses or contacts and have no need for a repeated eye doctor visit normally.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Conjunctival haemorrhage
- Hospital-Tage
- -
- Labordaten
- Went to Optometrist for an exam. Had to pay out of pocket. I don't normally go to an optometrist. I do not wear eye glasses or contacts and I have never had this happen before.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Very mild asthma. Had it as a child but grew out of it as an adult. Now only have an emergency inhaler but do not take it everyday.
- Andere Medikamente
- Prozac 60mg per day. Multi-vitamin
- Allergien
- No
- Vorherige Impfungen
- Swollen lymph node in armpit of injection site, flu-like symptoms
- Staat
- WA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
PT IS UNDER 18 Y/O AND RPH HAS GIVEN INJECTION OF (0.25 ML)MODERNA INSTEAD OF PFIZER BOOSTER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Moderna was given to a patient who was not of age to receive that vaccine. Due to the patient's age, he should have received a Pfizer vaccine. There were no known adverse effects at the time the vaccine was given or during observation following the vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No current or recent illnesses reported
- Vorgeschichte
- No health conditions reported
- Andere Medikamente
- No medications reported
- Allergien
- No allergies reported
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Nerve injury
Symptomtext
Patient called and said his entire back is burning. He described the pain as "nerve damage." He said it might be shingles, but he feels it over his entire back. He has not seen a doctor yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Burning sensation
- Hospital-Tage
- -
- Labordaten
- None as of yet.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chest discomfort
Cough
Hiatus hernia
Oropharyngeal discomfort
Symptomtext
Patient started coughing, pulse ox read 93 at that time. Pulse ox immediately went up to 97 when she stopped coughing. Patient complained of tightness in chest stating "Feels like hiatal hernia" and "nausea in throat" that was not present before vaccination. Patient vitals as follows: BP 138/72, HR 86, 02 93 Patient evaluated by APN provider in house and patient refused ER evaluation and refused EKG by provider, APN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest discomfort
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None listed by patient
- Vorgeschichte
- Asthma, Obesity
- Andere Medikamente
- Unknown
- Allergien
- None listed by patient
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- -
- Geschlecht
- U
- Eingang
- 18.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
5 expired doses administered from a vial greater than 12 hours post puncture; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (5 expired doses administered from a vial greater than 12 hours post puncture) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 016J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 13-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (5 expired doses administered from a vial greater than 12 hours post puncture). On 13-Jan-2022, EXPIRED PRODUCT ADMINISTERED (5 expired doses administered from a vial greater than 12 hours post puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that the vial was initially stored in the refrigerator on 10-Jan-2022, it was first punctured on 12-Jan-2022 at 03:45 pm and was kept in the refrigerator after punctured until it was administered. The vial did not undergo any temperature excursions. Total amount of time the vial was exposed to the room temperature was 8? to 25?C= 46? to 77?F. It was reported that 4 doses were booster doses and 1 dose was 2nd Moderna vaccine. No treatment medications were reported This case was linked to MOD-2022-451915 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
NO ADVERSE PATIENT 17 YEARS OLD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- NOT AVAILABLE
- Aktuelle Erkrankungen
- NOT AVAILABLE
- Vorgeschichte
- NOT AVAILABLE
- Andere Medikamente
- NOT AVAILABLE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 16.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
The patient presented his vaccine card to the technician which he got his first and second dose of Moderna so he filled out his card for moderna booster and so it was typed up for the Moderna booster, the patient stated he signed up for the Pfizer vaccine for his booster shot instead.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- 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
There were NO adverse patient reactions. Continually refrigerated Moderna vaccine was given past, recommended 12 hours of opening multi dose vial. Moderna manufacturer contacted regarding issue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
There were NO adverse patient reactions. Continually refrigerated Moderna vaccine was given past, recommended 12 hours of opening multi dose vial. Moderna manufacturer contacted regarding issue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
There were NO adverse patient reactions. Continually refrigerated Moderna vaccine was given past, recommended 12 hours of opening multi dose vial. Moderna manufacturer contacted regarding issue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
There were NO adverse patient reactions. Continually refrigerated Moderna vaccine was given past, recommended 12 hours of opening multi dose vial. Moderna manufacturer notified of issue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
there was no adverse affect at the time of vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate increased
Symptomtext
Patient stating having unexplained elevated heart rate/ high pulse that has not returned to normal yet
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate increased
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- unknown
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 09.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
MODERNA VACCINE WAS ADMINISTERED TO A PATIENT AGE 11YEARS OLD. The vaccine is only indicated for individuals age 18 and above.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 10.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Interchange of vaccine products
Symptomtext
Patient had admitted to already receiving 3 doses of Pfizer after receiving the first dose of Moderna for a total of 4 COVID vaccines. Patient received a full dose of Moderna as it was assumed it was the first COVID vacccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 08.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse event observed after 15 minute of injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- not known
- Allergien
- none
- Vorherige Impfungen
- -