- Staat
- TN
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 01.11.2023
- Impfdatum
- 27.10.2021
- Beginn
- 01.09.2023
- Tage bis Beginn
- 674,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aspiration pleural cavity
Atrial fibrillation
Bone sarcoma
Condition aggravated
Critical illness
Death
Debridement
Dyspnoea
Femur resection
General physical health deterioration
Infection
Pelvic resection
Pleomorphism
Procedural complication
Respiratory failure
Sepsis
Wound dehiscence
Symptomtext
She remained critically ill throughout the majority of her hospitalization. She required ongoing oxygen support. She had recurrent episodes of dyspnea and underwent thoracentesis on September 27th. She had intermittent episodes of atrial fibrillation with rapid ventricular response. She had recurrent sepsis with concern of ongoing infection in the wound the prompted her admission due to dehiscence. As she continued to fail to make any progress and actually continued to decline with recurrent sepsis and respiratory failure her family eventually decided for comfort care. She died on October 2nd at 5:36 a.m.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bone sarcoma
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Pleomorphic sarcoma of the left femur status post surgical resection January 2023 - status post left hemipelvectomy July 24th complicated by wound dehiscence and infection requiring multiple debridements Acute hypoxemic respiratory failure, improved Pneumonia, improved Acute blood loss anemia OSA Polymicrobial wound infection Pneumonia, improved Severe protein calorie malnutrition Chronic pain
- Vorgeschichte
- Atrial fibrillation Hypertension Obesity Chronic congestive heart failure OSA GERD Cholecystectomy Hysterectomy Gastric bypass Hip replacement Tumor resection Watchman
- Andere Medikamente
- -
- Allergien
- codeine
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 23.05.2023
- Impfdatum
- 13.12.2021
- Beginn
- 15.03.2022
- Tage bis Beginn
- 92,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Deep vein thrombosis
Hypotension
Pulmonary embolism
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE DVT OF LEFT LEG, UNSPECIFIED VEIN HYPOTENSION ACUTE PULMONARY EMBOLISM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 09.05.2023
- Impfdatum
- 20.10.2021
- Beginn
- 20.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Aortic valve incompetence
Cerebral septic infarct
Death
Endocarditis
Mitral valve incompetence
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration. In light of this, patient elected to receive additional dose of Moderna vaccine on Feb 1, 2022. On March 6, 2022 he was admitted to the hospital with infective endocarditis complicated by aortic and mitral valve failure and septic cerebral infarcts. On March 19, 2022, he passed away. He had risk factors for developing endocarditis and we don't believe there is an association between the improperly stored vaccine or revaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 94,0
- Geschlecht
- M
- Eingang
- 24.01.2023
- Impfdatum
- 10.11.2021
- Beginn
- 18.01.2023
- Tage bis Beginn
- 434,0
- Dosis
- 4
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Alanine aminotransferase normal
Anion gap
Anticoagulant therapy
Aspartate aminotransferase normal
Atrial fibrillation
Bacterial disease carrier
Bacterial test positive
Base excess
Basophil count decreased
Basophil percentage decreased
Benign prostatic hyperplasia
Bilirubin urine
Bladder scan
Blood albumin normal
Blood alkaline phosphatase normal
Blood bicarbonate increased
Blood bilirubin normal
Blood calcium normal
Symptomtext
Document Type: History and Physical Document Subject: History & Physical Note Performed By: DO on January 19, 2023 06:30 Verified By: DO on January 19, 2023 06:30 Encounter Info: Hospital, Inpatient, 01/18/23 - * Final Report * Chief Complaint flu-like symptoms History of Present Illness/Subjective A 95 year old male w/ hx of atrial fibrillation, dementia, stroke, recurrent/chronic UTI presents to the ED via EMS from assisted living facility c/o cough, fever, and generalized pain. Patient denies any dyspnea, chest pain, vomiting or diarrhea. In the ED he was found to be Influenza A positive and have evidence of uti on U/A, with recent hx of ESBL. HPI limited due to the patient being a poor historian, given it is difficult to determine if he is having urinary symptoms will cont treatment with Merrem and consider obtaining ID consult to help ascertain if this more likely represents colonization vs recurrent uti. Review of Systems unable to obtain ros due to the patient dementia. Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) Temp (CEL) 37.8 (36.9-37.8) Temp (FAHR) 100.0 (98.4-100.0), BP 135/64 (95-135)/(54-70), HR 103 (103-115), RR 18 (18-18), O2Sat 93 (91-93) Neurologic (most recent and range for last 24 hours) GCS 14(14-14) Patient Weight Current Daily Weight: 86.5 kg 01/19/23 Patient Height Constitutional: No acute distress, ill appearing, elderly male Eyes: no scleral icterus, no conjunctival injection HENT: no edema, atraumatic Neck: normal ROM Cardiovascular: tachycardic, regular rhythm, No edema Pulmonary: no respiratory distress, overall poor tidal volume, scattered fine crackles Abdomen: nondistended, no tenderness, no rebound, no guarding MSK: atraumatic, no deformities, no cyanosis Neurologic: motor function grossly intact, sensation grossly intact Skin: dry, warm Psych: calm and cooperative Assessment/Plan 1. Sepsis A41.9 2. Influenza A J10.1 3. BPH with obstruction/lower urinary tract symptoms N40.1 4. Recurrent UTI N39.0 most likely 2/2 influenza however cannot rule out acute on chronic UTI 2/2 esbl cover with merrem and tamiflu for now as symptoms began on day of presentation according to NH follow pancx maintain map >65 bladder scans prn monitor urine output supplemental O2 prn nebulizers prn 5. Atrial fibrillation I48.91 cont rate control patient is not on anticoag, possibly due to his age and risks of ich in the event of a fall 6. GERD (gastroesophageal reflux disease) K21.9 cont ppi 7. Hyperlipemia, mixed E78.2 cont statin 8. Dementia F03.90 cont home meds Orders: acetaminophen, 650 mg, Orally, Tablet, Q4H, PRN, Pain, Mild PO (1-3 out of 10)/Fever, 01/18/23 23:13:00 albuterol-ipratropium, 3 mL, Neb Inhal, Inhalation SOLN, Aerosol Treatment, Q6H, PRN, Shortness of Breath/Wheezing, 01/18/23 23:13:00 aspirin, 325 mg, Orally, Tab, Delayed Rel, Daily, 01/19/23 9:00:00 atenolol, 12.5 mg, Orally, Tablet, BID, 01/19/23 9:00:00 cetirizine, 10 mg, Orally, Tablet, QAM, PRN, Allergy Symptoms, 01/19/23 6:05:00 Dextrose 5% in Water 500 mL, Total Volume (mL) = 500, IV, 01/19/23 1:12:00, Other - See Comments, Clinical Weight finasteride, 5 mg, Orally, Tablet, Daily, 01/19/23 9:00:00 heparin, 5,000 Units, Subcutaneous, Injection, Q12, 01/19/23 6:00:00 Lactated Ringers 1,000 mL, Total Volume (mL) = 1,000, IV, 01/18/23 23:13:00, 50 mL/hr, Clinical Weight meropenem, 500 mg, IVPB, Injection, Q6H, Indication: Sepsis (ESBL or MDR History), 01/19/23 1:00:00, 200 mL/hr, Infuse Over 30 minutes, Total Volume (mL) = 100 mirtazapine, 7.5 mg, Orally, Tablet, At Bedtime, 01/19/23 21:00:00 morphine, 2 mg, IV Push, Injection, Q4H, PRN, Pain Moderate IV (4-6 out of 10), 01/18/23 23:13:00 ondansetron, 4 mg, IV Push, Injection, Q6H, PRN, Nausea/Vomiting IV - Use First, 01/18/23 23:13:00 oseltamivir, 30 mg, Orally, Capsule, BID, 01/19/23 9:00:00 pantoprazole, 20 mg, Orally, Tab, Delayed Rel, Daily, 01/19/23 9:00:00 polyethylene glycol 3350, 17 GM, Orally, Powder, Daily, 01/19/23 9:00:00 pravastatin, 40 mg, Orally, Tablet, At Bedtime, 01/19/23 21:00:00 Sodium Chloride 0.9% 250 mL, Total Volume (mL) = 250, IV, 01/19/23 1:12:00, Other - See Comments, Clinical Weight Sodium Chloride 0.9% 500 mL, Total Volume (mL) = 500, IV, 01/19/23 1:12:00, Other - See Comments, Clinical Weight 2000 mg Sodium, 225 gm Carb, 20 gm Saturated Fat Diet Admit to Inpatient Aspiration Precautions Auto Diff Call Blood Glucose Call Diastolic Blood Pressure Call Heart Rate Call Mental Status Changes Call O2 Saturation Call Respiratory Distress Call Respiratory Rate Call Systolic Blood Pressure Call Temperature Call Urine Output CBC w/Differential Comp Metabolic Panel DC SIRS Alert and Sepsis Screen Do Not (Specify) Dysphagia Screen by RN Fall Precautions Hgb A1C HPLC Bld QN Initiate IV Care Protocols As Appropriate Initiate Mobility Protocol Initiate Protocol Initiate Skin and Wound Care Protocol Intake + Output Strict Intermittent Catheterization Lactate Pl Venous QN Level of Care Magnesium SerPl QN Medical Service Meropenem Pharmacy Dosing Consult OT Evaluation and Treatment Patient Isolation Peripheral IV Insertion Procalcitonin PT Evaluation and Treatment Resp Evaluation or Assessment Resuscitation Status Sequential Compression Device Single Oxygen Saturation Telemetry Class III 24hr Recommendation Titrate FiO2 to Keep O2 Sat TSH w FreeT4 reflex Vital Signs Weight Weight Code Status Resuscitation Status - Ordered -- 01/18/23 23:13:00, Full Code Chronic Problem List Atherosclerosis of native artery of right lower extremity with rest pain Atrial fibrillation Balanoposthitis Bladder neck contracture BPH with obstruction/lower urinary tract symptoms Cholelithiasis Chronic UTI Colon polyps Critical lower limb ischemia Dementia Dysuria Exudative age-related macular degeneration of left eye with active choroidal neovascularization GERD (gastroesophageal reflux disease) History of stroke in adulthood Hyperlipemia, mixed Incomplete bladder emptying Lumbosacral disc disease Neurogenic bladder OSA (obstructive sleep apnea) Osteoarthritis Psoriasis PVC (premature ventricular contraction) Recurrent UTI Spondylolisthesis Tobacco use Urinary retention Procedure/Surgical History ?TURP (11/2018) ?Rt knee peroneal nerve release (07/22/2015) ?Bone density scan (06/24/2014) ?Colonoscopy (12/18/2012) ?Rt TKA (2000) ?Colonoscopy ?Dental implants ?EGD- bleeding ulcer with clamp ?Hemorroid surgery ?Inguinal Hernia Repair Surgical History Internal 09/11/2019 Bladder Neck Repair MD 11/28/2018 TUR Prostate MD 07/22/2015 Nerve Repair Peroneal (Right) MD Medications Home Medications (14) Active aspirin 325 mg oral delayed release tablet 325 mg = 1 Tablet, Orally, Daily atenolol 25 mg oral tablet 0.5 Tablet, Orally, BID cetirizine 10 mg oral tablet 10 mg = 1 Tablet, PRN, Orally, QAM Cranberry oral capsule 300 mg, Orally, BID finasteride 5 mg oral tablet See Instructions, Take 1 tablet by mouth once daily lactobacillus acidophilus oral capsule 1 Capsule, Orally, Daily mirtazapine 7.5 mg oral tablet 7.5 mg = 1 Tablet, Orally, At Bedtime Misc Supplement See Instructions, Australian Dream Cream for his back, uses PRN family sts it is an antihistamine and has herbs. From Pharmacy multivitamin Multiple Vitamins oral tablet 1 Tablet, Orally, Daily omeprazole 20 mg oral delayed release capsule 1 Capsule, Orally, Daily polyethylene glycol 3350 oral powder for reconstitution 17 GM, Orally, Daily pravastatin 40 mg oral tablet See Instructions, TAKE 1 TABLET BY MOUTH AT BEDTIME PreserVision AREDS 2 1 Capsule, Orally, BID triamcinolone 0.1% topical cream 1 App, Topical, TID, apply a thin film Active Scheduled Inpatient Medications aspirin, Tab, Delayed Rel, 325 mg, Orally, Daily, Start: 01/19/23 09:00:00 atenolol, Tablet, 12.5 mg, Orally, BID, Start: 01/19/23 09:00:00 finasteride, Tablet, 5 mg, Orally, Daily, Start: 01/19/23 09:00:00 heparin (heparin 5,000 units/0.5 mL injectable solution), Injection, 5,000 Units, Subcutaneous, Q12, Start: 01/19/23 06:00:00 meropenem, Injection, 500 mg, IVPB, Q6H, Indication: Sepsis (ESBL or MDR History), Start: 01/19/23 01:00:00 mirtazapine, Tablet, 7.5 mg, Orally, At Bedtime, Start: 01/19/23 21:00:00 oseltamivir (Tamiflu), Capsule, 30 mg, Orally, BID, Start: 01/19/23 09:00:00 pantoprazole, Tab, Delayed Rel, 20 mg, Orally, Daily, Start: 01/19/23 09:00:00 polyethylene glycol 3350 (polyethylene glycol 3350 oral powder for reconstitution), Powder, 17 GM, Orally, Daily, Start: 01/19/23 09:00:00 pravastatin, Tablet, 40 mg, Orally, At Bedtime, Start: 01/19/23 21:00:00 Lactated Ringers 1,000 mL IV 50 mL/hr Sodium Chloride 0.9% 500 mL IV Other - See Comments Dextrose 5% in Water 500 mL IV Other - See Comments Sodium Chloride 0.9% 250 mL IV Other - See Comments One-Time Medications Given 01/18/23 00:00:00 TO 01/19/23 06:29:39 None Reported PRN Medications (0600 - 0559) from 01/18 - 01/19 acetaminophen, 650 mg, Orally, Q4H, 0 Dose(s) albuterol-ipratropium, 3 mL, Neb Inhal, Q6H, 0 Dose(s) cetirizine, 10 mg, Orally, QAM, 0 Dose(s) morphine, 2 mg, IV Push, Q4H, 0 Dose(s) ondansetron, 4 mg, IV Push, Q6H, 0 Dose(s) Allergies Restoril (Difficulty Breathing) codeine (breathing difficulty, Vomiting) lovastatin (weakness) Social History Alcohol Current, Daily Electronic Cigarette/Vaping E-Cigarette Use Never. Home/Environment Lives with Spouse. Living situation: Home with assistance. Home equipment: Walker/Cane. Family/Friends available for support: Yes. Major illness in household: Yes. Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History High blood pressure..: Father. Stroke: Father. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 7.4 k/cumm (01/19/23 06:07:00) RBC: 4.44 million/cumm (01/19/23 06:07:00) Hgb: 13.7 GM/dL (01/19/23 06:07:00) Hct: 41.3 % (01/19/23 06:07:00) MCV: 93 fL (01/19/23 06:07:00) MCH: 30.8 pg (01/19/23 06:07:00) MCHC: 33.1 GM/dL (01/19/23 06:07:00) RDW: 14.2 % (01/19/23 06:07:00) Platelet: 209 k/cumm (01/19/23 06:07:00) MPV: 8 fL (01/19/23 06:07:00) Neutrophils %: 73 % (01/19/23 06:07:00) Lymphocytes %: 14 % (01/19/23 06:07:00) Monocytes %: 12 % (01/19/23 06:07:00) Eosinophils %: 1 % (01/19/23 06:07:00) Basophils %: 0 % (01/19/23 06:07:00) Absolute Neutrophil: 5.4 k/cumm (01/19/23 06:07:00) Absolute Lymphocyte: 1 k/cumm (01/19/23 06:07:00) Absolute Monocyte: 0.9 k/cumm (01/19/23 06:07:00) Absolute Eosinophil: 0.1 k/cumm (01/19/23 06:07:00) Absolute Basophil: 0 k/cumm (01/19/23 06:07:00) Chemistry: Sodium SerPl QN: 141 mmol/L (01/18/23 18:55:00) Potassium SerPl QN: 3.8 mmol/L (01/18/23 18:55:00) Chloride SerPl QN: 102 mmol/L (01/18/23 18:55:00) Carbon Dioxide SerPl QN: 30 mmol/L High (01/18/23 18:55:00) Anion Gap: 9 mmol/L (01/18/23 18:55:00) BUN SerPl QN: 12 mg/dL (01/18/23 18:55:00) Creatinine SerPl QN: 0.97 mg/dL (01/18/23 18:55:00) Estimated GFR (CKD-EPI, no race): 72 mL/min/1.73m2 (01/18/23 18:55:00) Estimated CRCL (CG): 50 mL/min Low (01/18/23 18:55:00) Glucose SerPl QN: 152 mg/dL High (01/18/23 18:55:00) Calcium Total SerPl QN: 10 mg/dL (01/18/23 18:55:00) Alkaline Phos SerPl QN: 76 Units/L (01/18/23 18:55:00) ALT SerPl QN: 20 Units/L (01/18/23 18:55:00) AST SerPl QN: 23 Units/L (01/18/23 18:55:00) Bilirubin Total SerPl QN: 0.4 mg/dL (01/18/23 18:55:00) Total Protein SerPl QN: 7.4 GM/dL (01/18/23 18:55:00) Albumin SerPl QN: 4 GM/dL (01/18/23 18:55:00) Troponin-I High Sensitivity: 8 ng/L (01/18/23 20:00:00) BNP Pl QN: 68 pg/mL (01/18/23 18:55:00) Lactate Venous Pl QN: 3.1 mmol/L High (01/18/23 22:10:00) pH Bld Venous QN: 7.38 (01/18/23 18:55:00) PCO2 Bld Venous QN: 49 mmHg (01/18/23 18:55:00) PO2 Bld Venous QN: <34 Low (01/18/23 18:55:00) Base Excess Bld Venous: 3 mmol/L High (01/18/23 18:55:00) Bicarb Bld Venous Calc: 29 mmol/L (01/18/23 18:55:00) O2 Sat Bld Venous Calc: 41 % (01/18/23 18:55:00) Patient Temperature: 37 DegC (01/18/23 18:55:00) Urine Studies: Color: Yellow (01/18/23 19:32:00) Clarity: Clear (01/18/23 19:32:00) Specific Gravity: 1.020 (01/18/23 19:32:00) pH: 6.0 (01/18/23 19:32:00) Protein: TRACE. Abnormal (01/18/23 19:32:00) Glucose: NEGATIVE (01/18/23 19:32:00) Ketones: NEGATIVE (01/18/23 19:32:00) Bilirubin: NEGATIVE (01/18/23 19:32:00) Hgb Ur: TRACE. Abnormal (01/18/23 19:32:00) Nitrite: POSITIVE Abnormal (01/18/23 19:32:00) Urobilinogen: NormalUro (01/18/23 19:32:00) Leukocyte Esterase Ur: MODERATE. Abnormal (01/18/23 19:32:00) WBC: 11-20 Abnormal (01/18/23 19:32:00) RBC: 3-5 Abnormal (01/18/23 19:32:00) Bacteria: Many Abnormal (01/18/23 19:32:00) Squamous Epithelial: Few (01/18/23 19:32:00) All Other Labs: COVID 19 Specimen Source: Nasopharyngeal (01/18/23 18:55:00) Coronavirus SARS-CoV2 Rapid: Not Detected (01/18/23 18:55:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (01/18/23 18:55:00) Rapid Influenza A PCR: Detected Abnormal (01/18/23 18:55:00) Rapid Influenza B PCR: Not Detected (01/18/23 18:55:00) Urine CX: POS Critical (01/14/23 15:58:00) Diagnostics Radiology Results - Last 24 hours Across Visits 01/18/2023 19:31 - XR Chest PA or AP Portable IMPRESSION: No acute findings.Thank you for consulting with Radiology. Healthcare providerswishing to discuss this case further can contact the ER Reading Room. Signature Line Electronically Signed on 01/19/23 06:30 ________________________________________________________ DO
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Coma scale
- Hospital-Tage
- -
- Labordaten
- Molecular Diagnostic Tests COVID 19 Specimen Source Nasopharyngeal Nasopharyngeal Coronavirus SARS-CoV2 Rapid * Not Detected * Not Detected Candida auris DNA PCR Not Detected Candida auris DNA PCR Interp * Candida auris DNA PCR Interp Viral FS Rapid Influenza Method PCR - Liat Rapid Influenza A PCR * (A) Detected Rapid Influenza B PCR * Not Detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 16.09.2022
- Impfdatum
- 16.09.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 107,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Death
General physical health deterioration
SARS-CoV-2 test positive
Symptomtext
pt lives at facility; pt had a positive COVID test on 1/21/22 in the facility; pt recovered from COVID; DNR; pt's overall condition continued to decline; hospice referral; pt passed away in the facility on 3/11/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CVA with Right sided weakness, COPD, GERD, IBS, DMT2, PVD, PAD, HLD, HTN
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 27.06.2022
- Impfdatum
- 19.10.2021
- Beginn
- 09.02.2022
- Tage bis Beginn
- 113,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute respiratory failure
Arthralgia
Brain oedema
COVID-19
Cerebral artery occlusion
Cerebrovascular accident
Computerised tomogram head abnormal
Death
Endotracheal intubation
Intensive care
Mechanical ventilation
Neck pain
Pain in extremity
SARS-CoV-2 test positive
Skull X-ray
Symptomtext
Patient was admitted on 02/18/2022 with ventilator dependent acute resp failure d/t stroke. On 02/02/2022 patient noted to be Covid Positive. Since then patient had lingering neck shoulder and arm pain. Patient was intubated and admitted to ICU. Admitted with acute CVA due to left MCA occlusion complicated by malignant cerebral edema and acute hypoxic respiratory failure. Patient was transitioned to comfort care and expired on 02/27/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 9,0
- Labordaten
- CT brain 02/18/2022 proximal left MCA occlusion with changes in grey white differentiation consistent with acute stroke. Xray 02/18/2022: foreign body projecting over the hypopharynx likely representing dental hardware.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 21.06.2022
- Impfdatum
- 27.09.2021
- Beginn
- 13.02.2022
- Tage bis Beginn
- 139,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Acute kidney injury
Asymptomatic COVID-19
Chest X-ray abnormal
Computerised tomogram abdomen abnormal
Culture urine positive
Escherichia test positive
Hypotension
Intensive care
Lung infiltration
Pyelonephritis
SARS-CoV-2 test positive
Septic shock
Urinary tract infection
Urine output decreased
Symptomtext
Patient was admitted 2/13 with hypotension, decreased urine output, found to have UTI & septic shock, given 4 L fluid bolus & started on pressors. He was also found to be COVID-19 positive. CT scan of the abdomen and pelvis revealed no evidence of obstructive uropathy but was suggestive of pyelonephritis/left perinephric and perivesicular stranding. Chest x-ray showed mild interstitial infiltrates. Patient received vancomycin, cefepime and azithromycin in the emergency room and was admitted to ICU. he patient was weaned off dopamine and vasopressin drips and transferred out of ICU on 02/16/2022. Urine culture grew E coli, pansensitive, and pt discharged on 7 day course of ciprofloxacin Patient's AKI also improved. Pt continued to be asymptomatic from COVID-19 and wanted to go home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Septic shock
- Hospital-Tage
- 4,0
- Labordaten
- Positive COVID 19 test on 02/13/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Date Unknown Arthritis 5/20/22 Benign prostatic hyperplasia with urinary obstruction Date Unknown Bladder cancer (HCC) Date Unknown CAD (coronary artery disease) Date Unknown CKD (chronic kidney disease) stage 3, GFR 30-59 ml/min (HCC) Date Unknown COPD (chronic obstructive pulmonary disease) (HCC) Date Unknown Coronary atherosclerosis Date Unknown GERD (gastroesophageal reflux disease) Date Unknown High cholesterol Date Unknown Hypertension Date Unknown MI (myocardial infarction) (HCC) Date Unknown Renal mass
- Andere Medikamente
- albuterol (VENTOLIN HFA) 108 (90 BASE) MCG/ACT HFA inhaler amLODIPine (NORVASC) 2.5 MG tablet aspirin (HALFPRIN) 81 MG tablet atorvastatin (LIPITOR) 20 MG tablet clopidogrel (PLAVIX) 75 MG tablet Cyanocobalamin (VITAMIN B-12) 1000 MCG
- Allergien
- no known drug allergies
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 12.10.2021
- Beginn
- 22.02.2022
- Tage bis Beginn
- 133,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
Hypophagia
Mental status changes
Pneumonia
Renal failure
Therapy non-responder
Symptomtext
Patient admitted 03/08/2022 after he stopped eating and drinking after having contracted Covid-19 at home. He was admitted to the hospitalist service and he was in renal failure as well as having an AMS and PNA. His renal function worsened and he was not responding to therapy, family decided to make him DNR/Comfort care. Patient expired on 03/11/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 23.03.2021
- Beginn
- 01.02.2022
- Tage bis Beginn
- 315,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Asymptomatic COVID-19
Death
SARS-CoV-2 test positive
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 02/10/2021, 03/10/2021, and 09/23/2021. They first tested positive via antigen test on 02/01/2022 as a part of assisted living facility outbreak testing. At that time, they were described as "asymptomatic." They tested positive for COVID-19 again on 02/13/2022 and 02/24/2022 when being admitted to hospital. They remained hospitalized until their death on 03/04/2022. The individual had listed allergies to Measles Vaccine, Mumps Vaccine, Rubella Vaccine, MMR Vaccine, and Zoster Vaccine but the nature/reaction of these allergies was not listed in the health link system.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 8,0
- Labordaten
- Positive COVID-19 tests x3 despite being vaccinated.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Peripheral Edema, Congestive Heart Failure, Diabetes Mellitus, previous kidney transplant The individual was a resident of an assisted living facility at the time of the adverse event.
- Andere Medikamente
- -
- Allergien
- Reported allergies to penicillin (reaction: unknown); Measles Vaccine (reaction: unknown); Rubella Vaccine (Reaction: unknown); Mumps Vaccine (reaction: Unknown); Vancomycin (Reaction: hives); Zoster Vaccine (reaction: unknown); MMR Vaccine (reaction: unknown/other);
- Vorherige Impfungen
- Reported allergies to the following vaccines: Measles; Mumps; Rubella; MMR; and Zoster. The nature/reaction to these allergies i
- Staat
- SD
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 20.09.2021
- Beginn
- 14.02.2022
- Tage bis Beginn
- 147,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
Acute respiratory distress syndrome
COVID-19
Death
Dehydration
Diarrhoea
Ischaemic stroke
Pneumonia bacterial
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
This is an instance of breakthrough COVID-19 after which death occurred. The individual was vaccinated with the Moderna product on 03/04/2021, 04/01/2021, and 09/20/2021. They tested positive for COVID-19 on 02/14/2022 and again on 02/21/2022. They were admitted to hospital 02/14/2022 and transferred to a different hospital on 02/19/2022 for a higher level of care. They experienced multiple complications, including ARDS, secondary bacterial pneumonia, dehydration due to acute diarrhea, acute ST elevation myocardial infarction of anterior wall, and acute stroke due to ischemia. The individual was transitioned to comfort care only on 03/04/2022 and they died later on the same day on 03/04/2022. This individual was immunosuppressed due to medication use.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 18,0
- Labordaten
- Positive COVID-19 tests x2 on 02/14/2022 and 02/21/2022 despite being vaccinated.
- Aktuelle Erkrankungen
- Acute diarrhea with dehydration (C. Diff negative)
- Vorgeschichte
- Hypertension, Rheumatic Lung Disease, Immunodeficiency due to medication
- Andere Medikamente
- Rituxan
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 15.03.2022
- Impfdatum
- 30.08.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 46,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Anticoagulant therapy
COVID-19
COVID-19 pneumonia
Cardiac arrest
Chest X-ray abnormal
Death
Dyspnoea
Fibrosis
Diarrhoea
Dyspnoea exertional
General physical health deterioration
Positive airway pressure therapy
SARS-CoV-2 test positive
Insulin therapy
Intensive care
Myalgia
Pancreatic failure
Pyrexia
Symptomtext
Pt presented to hospital via EMS with sob and dyspnea on exertion; pmh of renal and pancreas transplant on immunosuppression, dm, htn, hld, gerd; pt visited urgent care for diarrhea and muscle aches and found to be COVID positive on 10/15 and told to isolate; sob got progressively worse which brought her to the hospital; initial O2 sat was in 50s; pt was febrile at 39.1 C, bp 128/74, hr 117, rr 28 and satting low 90s hfnc 40 L at 100% FiO2. Dx?d with pneumonia due to COVID-19; former smoker; allergies: flagyl; treatments dexamethasone, baricitnib, guifenesin codeine cough syrup; pancreas began to fail; pt started on insulin; pt was sent to icu, proned; required bipap and vaptherm and put on anticoagulation; pt continued to decline and CXR worsened; bipap removed 11/09 after discussion with family and pt became asystole shortly after; pt passed away the afternoon of 11/09/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 20,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 03.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Patient's wife had a virtual provider with APRN on 022222 and reported that her husband (patient) "passed away three weeks after getting the booster". The patient reportedly had no other chronic health problems but reportedly took doxazosin according to what was reported to the virtual provider. No autopsy was performed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 02.04.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 278,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
COVID-19
Lung opacity
Pneumonia
SARS-CoV-2 test
SARS-CoV-2 test positive
Symptomtext
ACUTE MYOCARDIAL INFARCTION; PNEUMONIA; LUNG OPACITY; SARS-COV-2 TEST POSITIVE; COVID-19; This spontaneous report received from a health care professional via a Regulatory Authority Vaccine Adverse Event Reporting System (VAERS) (VAERS ID 2035903) on 28-JAN-2022 and concerned a 62 year old female of unspecified race and ethnicity. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration, batch number: 041A21A expiry: unknown) dose was not reported, dose number in series was 01, 01 in total administered on 02-APR-2021 for unknown indication. On an unspecified date, following vaccination with covid-19 vaccine ad26.cov2.s, it was unknown whether patient had any adverse events (dose number in series was 01). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient additionally received non-company suspect vaccine MRNA 1273 ( form and route of administration were not reported, batch number: 045C21A expiry: unknown) dose was not reported, dose number in series was 02, administered on 02-NOV-2021 for an unspecified indication. On 05-JAN-2022, the patient experienced severe acute respiratory syndrome coronavirus (SARS-CoV-2) infection. On the same day, coronavirus disease (Covid-19) polymerase chain reaction (PCR) test result was positive. On 09-JAN-2022, the patient had acute myocardial infarction, pneumonia, lung opacity. The patient was admitted on 11-JAN-2022 and she was discharged on 14-JAN-2022. She was hospitalized for 4 days. Patient was hospitalized for non-ST-elevation myocardial infarction (NSTEMI) suspected pneumonia in the anterior right upper lobe accounted for consolidative opacities. She consulted for positive COVID-19 and recommendations included a three day course of remdesivir (dose number in series was 02). The outcome of the acute myocardial infarction, covid-19, lung opacity, pneumonia and SARS-CoV-2 test positive was not reported. This report was serious (Hospitalization Caused / Prolonged). This report was associated with product quality complaint: 90000214995. The suspected product quality complaint has been confirmed to be the reported allegation could not be determined. a manufacturing related root cause could not be identified. based on the PQC evaluation/investigation performed. Additional information was received from Central Complaint Vigilance Department on 03-FEB-2022. The following information was updated and incorporated into case narrative: Product Quality Complaint investigation result.; Sender's Comments: V2: Follow up information in this version updated Product quality complaint investigation result. The follow up information does not change the causality of the previous report 20220156997 - covid-19 vaccine ad26.cov2.s - acute myocardial infarction, pneumonia, covid-19, lung opacity, and SARS-CoV-2 test positive. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 4,0
- Labordaten
- Test Date: 20220105; Test Name: COVID-19 PCR test; Result Unstructured Data: positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 02.04.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 278,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
COVID-19
Lung opacity
Pneumonia
SARS-CoV-2 test
SARS-CoV-2 test positive
Symptomtext
ACUTE MYOCARDIAL INFARCTION; PNEUMONIA; LUNG OPACITY; SARS-COV-2 TEST POSITIVE; COVID-19; This spontaneous report received from a health care professional via a Regulatory Authority Vaccine Adverse Event Reporting System (VAERS) (VAERS ID 2035903) on 28-JAN-2022 and concerned a 62 year old female of unspecified race and ethnicity. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration, batch number: 041A21A expiry: unknown) dose was not reported, dose number in series was 01, 01 in total administered on 02-APR-2021 for unknown indication. On an unspecified date, following vaccination with covid-19 vaccine ad26.cov2.s, it was unknown whether patient had any adverse events (dose number in series was 01). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient additionally received non-company suspect vaccine MRNA 1273 ( form and route of administration were not reported, batch number: 045C21A expiry: unknown) dose was not reported, dose number in series was 02, administered on 02-NOV-2021 for an unspecified indication. On 05-JAN-2022, the patient experienced severe acute respiratory syndrome coronavirus (SARS-CoV-2) infection. On the same day, coronavirus disease (Covid-19) polymerase chain reaction (PCR) test result was positive. On 09-JAN-2022, the patient had acute myocardial infarction, pneumonia, lung opacity. The patient was admitted on 11-JAN-2022 and she was discharged on 14-JAN-2022. She was hospitalized for 4 days. Patient was hospitalized for non-ST-elevation myocardial infarction (NSTEMI) suspected pneumonia in the anterior right upper lobe accounted for consolidative opacities. She consulted for positive COVID-19 and recommendations included a three day course of remdesivir (dose number in series was 02). The outcome of the acute myocardial infarction, covid-19, lung opacity, pneumonia and SARS-CoV-2 test positive was not reported. This report was serious (Hospitalization Caused / Prolonged). This report was associated with product quality complaint: 90000214995. The suspected product quality complaint has been confirmed to be the reported allegation could not be determined. a manufacturing related root cause could not be identified. based on the PQC evaluation/investigation performed. Additional information was received from Central Complaint Vigilance Department on 03-FEB-2022. The following information was updated and incorporated into case narrative: Product Quality Complaint investigation result.; Sender's Comments: V2: Follow up information in this version updated Product quality complaint investigation result. The follow up information does not change the causality of the previous report 20220156997 - covid-19 vaccine ad26.cov2.s - acute myocardial infarction, pneumonia, covid-19, lung opacity, and SARS-CoV-2 test positive. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 4,0
- Labordaten
- Test Date: 20220105; Test Name: COVID-19 PCR test; Result Unstructured Data: positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 02.04.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 278,0
- Dosis
- 2
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute myocardial infarction
COVID-19
Lung opacity
Pneumonia
SARS-CoV-2 test
SARS-CoV-2 test positive
Symptomtext
ACUTE MYOCARDIAL INFARCTION; PNEUMONIA; LUNG OPACITY; SARS-COV-2 TEST POSITIVE; COVID-19; This spontaneous report received from a health care professional via a Regulatory Authority Vaccine Adverse Event Reporting System (VAERS) (VAERS ID 2035903) on 28-JAN-2022 and concerned a 62 year old female of unspecified race and ethnicity. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient previously received covid-19 vaccine ad26.cov2.s (suspension for injection, route of administration, batch number: 041A21A expiry: unknown) dose was not reported, dose number in series was 01, 01 in total administered on 02-APR-2021 for unknown indication. On an unspecified date, following vaccination with covid-19 vaccine ad26.cov2.s, it was unknown whether patient had any adverse events (dose number in series was 01). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient additionally received non-company suspect vaccine MRNA 1273 ( form and route of administration were not reported, batch number: 045C21A expiry: unknown) dose was not reported, dose number in series was 02, administered on 02-NOV-2021 for an unspecified indication. On 05-JAN-2022, the patient experienced severe acute respiratory syndrome coronavirus (SARS-CoV-2) infection. On the same day, coronavirus disease (Covid-19) polymerase chain reaction (PCR) test result was positive. On 09-JAN-2022, the patient had acute myocardial infarction, pneumonia, lung opacity. The patient was admitted on 11-JAN-2022 and she was discharged on 14-JAN-2022. She was hospitalized for 4 days. Patient was hospitalized for non-ST-elevation myocardial infarction (NSTEMI) suspected pneumonia in the anterior right upper lobe accounted for consolidative opacities. She consulted for positive COVID-19 and recommendations included a three day course of remdesivir (dose number in series was 02). The outcome of the acute myocardial infarction, covid-19, lung opacity, pneumonia and SARS-CoV-2 test positive was not reported. This report was serious (Hospitalization Caused / Prolonged). This report was associated with product quality complaint: 90000214995. The suspected product quality complaint has been confirmed to be the reported allegation could not be determined. a manufacturing related root cause could not be identified. based on the PQC evaluation/investigation performed. Additional information was received from Central Complaint Vigilance Department on 03-FEB-2022. The following information was updated and incorporated into case narrative: Product Quality Complaint investigation result.; Sender's Comments: V2: Follow up information in this version updated Product quality complaint investigation result. The follow up information does not change the causality of the previous report 20220156997 - covid-19 vaccine ad26.cov2.s - acute myocardial infarction, pneumonia, covid-19, lung opacity, and SARS-CoV-2 test positive. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 4,0
- Labordaten
- Test Date: 20220105; Test Name: COVID-19 PCR test; Result Unstructured Data: positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 27.10.2021
- Beginn
- 07.02.2022
- Tage bis Beginn
- 103,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Acute respiratory failure
COVID-19
Inappropriate schedule of product administration
Leukocytosis
Pulmonary embolism
SARS-CoV-2 test positive
Symptomtext
Patient received Moderna COVID-19 vaccine on 2/5/2021 (batch/lot# 013M20A), 3/6/2021 (batch/lot# 029A21A) and 10/27/2021 (batch/lot# 045C21A). On 1/24/2022, patient had an external positive result for COVID-19. On 2/7/2022, patient admitted to our inpatient facility with acute respiratory failure with hypoxia, acute pulmonary embolism, leukocytosis, acute kidney injury and COVID-19 positive result. As of today (2/8/2022), patient still admitted in the med/surgery unit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 1,0
- Labordaten
- COVID-19 status positive 1/24/2022 (external result) and 2/7/2022 (internal result).
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Right renal cell carcinoma s/p partial nephrectomy, HTN, OSA, metastatic colon cancer near obstructing cecal mass (focal invasion, omental carcinomatosis, focal peritoneal implant in the low pelvis, liver lesion), on FOLFOX regimen
- Andere Medikamente
- Acetaminophen, Dronabinol, Duloxetine, Loperamide, Lorazepam, Metoprolol ER, Ondansetron, Prochlorperazine
- Allergien
- Hydrochlorothiazide
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- U
- Eingang
- 04.02.2022
- Impfdatum
- 23.09.2021
- Beginn
- 27.01.2022
- Tage bis Beginn
- 126,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
COVID-19 pneumonia
Death
Endotracheal intubation
Renal impairment
SARS-CoV-2 test positive
Serratia infection
Stenotrophomonas infection
Unresponsive to stimuli
Urinary tract infection
Symptomtext
Moderna COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Moderna Vaccines on 01/29/21, 3/6/2021 and 9/23/2021. COVID + on 1/11/22. Presented to ED on 1/16/2022, intubated and sedated after being found unresponsive at home with O2 in 50s. Recently discharged on 2.5L NC from outside facility for COVID PNA (1/11 - 1/15). Treated with solumedrol, rocephin, and remdesivir at outside facility. Once admitted, found to have complicated UTI with stenotrophomonas maltophilia and Serratia rubidaea. treated with cefepime then ceftriaxone. Renal function continued to worsen despite treatments and supportive measures. DNAR. Expired 1/27/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 11,0
- Labordaten
- 1/16/22 Covid + : nasophayrnx
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HFpEF, COPD, CKD4, HTN, HLD, DM2, renal transplant
- Andere Medikamente
- amlodpine, cyclosporine, furosemide, mirabegron, mycophenolate mofetil
- Allergien
- Bactrim, aspirin, ceftazidime, gemfibrozol, metformmin, NSAIDS tolmentin
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 96,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 30.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Agitation
Blood test
COVID-19
COVID-19 pneumonia
Chest X-ray
Confusional state
Cough
Death
Fatigue
General physical health deterioration
Patient restraint
Renal failure
Renal function test
SARS-CoV-2 test positive
Symptomtext
starting day after booster shot: extreme fatigue with cough for two days, on the third day 12/03/2021 was tested positive for CoVid 19. Went to the ER on 12/06/2021 with renal failure and CoVid pneumonia. Was administered Remdesivir for two days and became confused and agitated to the point of being restrained. Remdesivir was stopped. Released from the hospital on 12/16/2021, tested negative for CoVid 19 on 12/31/2021. Continual decline until death on Jan. 7, 2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 8,0
- Labordaten
- chest X-rays, maybe CT scan, kidney function tests, blood tests
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- multiple myeloma in remission, no symptoms COPD, minimal symptoms
- Andere Medikamente
- Norvasc, Calcium/Vitamin D3, senior multi-vitamin, Lexipro, vitamin C gummies, Miralax, probiotic, zinc tablet, Tylenol as needed, compazine as needed
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 10.11.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 33,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Computerised tomogram thorax
Deep vein thrombosis
Pulmonary embolism
Ultrasound Doppler abnormal
Symptomtext
Patient developed left lower extremity DVT and subsequent PE. He has no other risk factors for thrombosis. No recent surgeries or immobilizations. No chronic medical conditions. Of note, the patient also developed a Bell's Palsy after the first dose of his Moderna Vaccine which was given on 10/13/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- CT PE on 12/15 showing large, but nonocclusive, pulmonary embolism burden bilaterally, lower extremity duplex ultrasound showing DVT in the left lower extremity involving the peroneal veins as well as the popliteal veins
- Aktuelle Erkrankungen
- Bell's Palsy (thought to be related to first dose of vaccine)
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- Bell's Palsy after first dose of Moderna vaccine on 10/13/21
- Staat
- PA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 13.12.2021
- Impfdatum
- 27.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Catheterisation cardiac abnormal
Chest pain
Chills
Coronary angioplasty
Coronary arterial stent insertion
Coronary artery thrombosis
Cough
Electrocardiogram
Myocardial infarction
Nasopharyngitis
Symptomtext
I received the Covid 19 Booster dose on Wednesday 10-27-21. The next morning I had minor cold like symptoms that started with chills and turned into a cough by Saturday 10-30-21. My chest began to hurt on that date and I presumed it was because of the cough. The chest pain and cough continued to get worse so I went to Urgent care on Tuesday 11-2-21. They performed an EKG and provided a cough medicine. The chest pain continued to get worse until finally on 11-8-21 I was convinced that I was having a heart attack. I went to the ER at Hospital. They had to perform a heart catherization and put in a stint because of a blood clot in my LAD artery. Dr said that there wasn't any plaque or buildup, but rather a bloodclot that caused the heart attack.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 4,0
- Labordaten
- 11-8-21 bloodwork, EKG, Heart catherization and Angioplasty
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 31,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Catheterisation cardiac
Chest pain
Coronary arterial stent insertion
Electrocardiogram abnormal
Impaired work ability
Myocardial infarction
Symptomtext
I started having chest pains early in the morning. On November 29, 2021 at about 7:30pm I went to the ER. I had severe chest pains. The doctor said I was having a heart attack. I had stents punt in, and they did a cardio catherization. I was then hospitalized for 2 days. I was prescribed Atorvastatin 40mg 1xday, Aspirin 81mg 1xday, Carvedilol 3.125mg 2xday, and Brilinta 90mg 2xday. I am still out of work and recovering from this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 2,0
- Labordaten
- EKG- showed I was having a heart attack (November 2021)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- History of Heart Disease (Present) History Gout
- Andere Medikamente
- Alopurinol 100mg 1xday
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 07.09.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 77,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
Endotracheal intubation
Intensive care
SARS-CoV-2 test positive
Unresponsive to stimuli
Symptomtext
Patient presented from skilled nursing facility on 11/23/2021 with unresponsiveness. He was diagnosed with COVID-19 infection on 11/18/2021. Patient was intubated and admitted to intensive care unit. Patient remained in critical condition during admission and was changed to comfort measures only. He expired on 11/30/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 7,0
- Labordaten
- COVID-19 test positive 11/23/2021.
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- Arthritis, congestive heart failure, COPD, hypertension, hyperlipidemia, insomnia, mental disorder, obesity, peripheral vascular disease
- Andere Medikamente
- acetaminophen (TYLENOL) 325 MG tablet albuterol (VENTOLIN HFA) 108 (90 BASE) MCG/ACT HFA inhaler atorvastatin (LIPITOR) 20 MG tablet bisacodyl (DULCOLAX) 10 MG suppository bumetanide (BUMEX) 2 MG tablet docusate sodium (COLACE) 100 MG capsu
- Allergien
- Dilaudid, flagyl, morphine
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 21.10.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 22,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blindness unilateral
Cerebrovascular accident
Cognitive disorder
Computerised tomogram normal
Dysarthria
Dyspnoea
Heart rate irregular
Hemiparesis
Hypertension
Vomiting
Symptomtext
Events: Vision loss in right eye, loss of muscle function on right side, slurred speech, slow comprehension, high blood pressure, irregular heart beat, difficulty breathing, and vomiting. Taken to ER at 8 pm and given Zofran . Syptoms remained. Life flighted. Ct scan ran and normal. Released two days later with follow up to neurologist for stroke.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Complex migraine at age of 15, ADHD, head trauma at 21.
- Andere Medikamente
- Ritalin 10 mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 09.09.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 82,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Death
Symptomtext
Patient was dx with COVID-19, was hospitalized and exipred.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 45,0
- Labordaten
- -
- Aktuelle Erkrankungen
- COVID-19, PE.
- Vorgeschichte
- CHF, morbid obesity, DM.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 27.10.2021
- Impfdatum
- 21.06.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 123,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Death
SARS-CoV-2 test positive
Symptomtext
Pt died after testing positive for COVID-19 on 10/4/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 18,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Sever history of pulmonary HTN, ILD, chronic hypoxia on 8L NC as baseline, HTN, T2 DM on insulin, afib, and CKD.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 02.09.2021
- Impfdatum
- 26.08.2021
- Beginn
- 27.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cerebrovascular accident
Dyslipidaemia
Minimal residual disease
Thymectomy
Symptomtext
Left doctors office two weeks after 2nd vaccine. Does have factors tobacco use, HTN, dilarid and not a ASA. Thymectomy and minimal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension Tobacco use Hyperlipidemia
- Andere Medikamente
- Benezepril Atorvesatin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 12.07.2021
- Impfdatum
- 07.07.2021
- Beginn
- 12.07.2021
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac arrest
Extra dose administered
Symptomtext
Patient unknowingly received 4 doses of covid vaccine and had a cardiac arrest on 7/12/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 10.09.2023
- Impfdatum
- 27.01.2021
- Beginn
- 01.02.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Bradycardia
Cervical spinal stenosis
Chills
Dyspnoea
Dyspnoea exertional
Fatigue
Gastritis
Herpes zoster
Iron deficiency anaemia
Irritability
Laboratory test abnormal
Loss of employment
Nausea
Nystagmus
Occipital neuralgia
Pallor
Peripheral coldness
Small intestinal obstruction
Symptomtext
?Moderna COVID-19 Vaccine EUA? Syncopy/ Tachycardia/ Bradycardia/ POSSIBLE LEFT ATRIAL ENLARGEMENT/ Iron Deficiency Anemia/ partial small bowel obstruction/ gastritis/ Hives, Shingles/ Coarse tremors/ transient global amnesia/ Occipital neuralgia/ Nystagmus/persistent irritability/ Cervical spinal stenosis / dyspnea on exertion/ fatigue/ Shortness of breath/ Chills/ Nausea with vomiting/ cool, pale skin/Moderate to severe tendinosis of the supraspinatus and mild to moderate grade tendinosis of the infraspinatus tendons left shoulder/ Occipital neuralgia/ Mild central canal stenosis/ Abnormal labatory results of unknown orgion Multiple physician visits/ hospital stay/ Emergancy room visits/ Surgeries/ loss of work from 03/21/2021 to present
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 23.05.2023
- Impfdatum
- 12.11.2021
- Beginn
- 18.03.2022
- Tage bis Beginn
- 126,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Deep vein thrombosis
Symptom recurrence
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE DVT OF RIGHT LEG, UNSPECIFIED VEIN ACUTE DVT OF LEFT LEG, UNSPECIFIED VEIN ACUTE DVT, UNSPECIFIED VEIN 3/19/2022 -- RECURRENCE OF SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 13.03.2023
- Impfdatum
- 08.10.2021
- Beginn
- 27.02.2023
- Tage bis Beginn
- 507,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Seizure like phenomena
Symptomtext
hospitalized for 5 days for seizure-like activity, incidentally found to be positive for COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure like phenomena
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CAD, HTN, NPH s/o VP shunt
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 23.08.2022
- Impfdatum
- 26.01.2021
- Beginn
- 25.06.2022
- Tage bis Beginn
- 515,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
Blood sodium decreased
COVID-19
Hyperglycaemia
Hypertension
Hyponatraemia
Intensive care
Oedema
Symptomtext
Diagnosed with covid on 6/12. Received Paxlovid. Admitted on 6/25/22 for hyponatremia, weakness, edema, hyperglycemia, hypertension. Sent to ICU from the ED sodium level 119. Sent back to floor 6/26 and was discharged on 7/5/22. Readmitted on 8/18/22 for hypertension and is still currently in the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 07.05.2022
- Impfdatum
- 27.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blindness
Chest pain
Cold sweat
Diarrhoea
Dyspnoea
Fatigue
Pain
Paralysis
Speech disorder
Symptomtext
I woke up paralyzed. I couldn't move, see or talk. I had extreme pain in my body, particularly in my chest. I had difficulty breathing. I thought I was going to die. Then, I'm guessing 20 minutes later, I was finally able to move and I made my way to the bathroom where I had a lot of diarrhea. When I got back to bed I was having cold sweats. I was exhausted and all I could do was get back into bed. I realized now that my husband should have taken me to the emergency room. But he didn't think of it and I was too exhausted to do anything other than sleep.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- -
- Labordaten
- Did not go to the hospital.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 16.08.2021
- Beginn
- 17.09.2021
- Tage bis Beginn
- 32,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Myocarditis
Troponin
Symptomtext
symptoms were numbness in his left arm and pain in the chest / Myocarditis; This spontaneous case was reported by a consumer and describes the occurrence of MYOCARDITIS (symptoms were numbness in his left arm and pain in the chest / Myocarditis) in a 29-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 050F21A and 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 17-Sep-2021, the patient experienced MYOCARDITIS (symptoms were numbness in his left arm and pain in the chest / Myocarditis) (seriousness criteria hospitalization and medically significant). The patient was hospitalized from 17-Sep-2021 to 19-Sep-2021 due to MYOCARDITIS. The patient was treated with IBUPROFEN at an unspecified dose and frequency. On 18-Nov-2021, MYOCARDITIS (symptoms were numbness in his left arm and pain in the chest / Myocarditis) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In September 2021, Troponin: high (High) Troponin elevated. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. Treatment medications included unspecified blood thinner. The patient called to report that he had myocarditis after getting the second dose of the Moderna Covid-19 vaccine. His symptoms were pain in the chest, numbness in his left arm.. Lab results included, troponin elevated. He was told that he has myocarditis when the lab results came in. Patient was hospitalized from 17-Sep-2021 to 19-Sep-2021. Company Comment: This case refers to a 29-year-old male patient with no known medical history who experienced the expected event of Myocarditis approximately 4 days after the second dose of mRNA-1273 vaccine. No causality assessment was provided by the reporter. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This case refers to a 29-year-old male patient with no known medical history who experienced the expected event of Myocarditis approximately 4 days after the second dose of mRNA-1273 vaccine. No causality assessment was provided by the reporter. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 3,0
- Labordaten
- Test Date: 202109; Test Name: Troponin; Result Unstructured Data: Troponin elevated
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 27,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asymptomatic COVID-19
Fall
SARS-CoV-2 test positive
Syncope
Symptomtext
Patient presented to emergency department on 12/2/2021 following a fall and syncope episode at home. She was found to be COVID-19 positive during admission screening. She remained asymptomatic during admission and did not require treatment. She was discharged home on 12/3/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- 1,0
- Labordaten
- COVID-19 test positive on 12/2/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension, seizure, COPD, multiple sclerosis, arthritis, angina, hyperlipidemia,
- Andere Medikamente
- acetaminophen (TYLENOL) 325 MG tablet albuterol (VENTOLIN HFA) 108 (90 BASE) MCG/ACT HFA inhaler aspirin (HALFPRIN) 81 MG tablet atorvastatin (LIPITOR) 40 MG tablet HYDROcodone-acetaminophen (NORCO) 5-325 MG tablet lamoTRIgine (LAMICTAL) 10
- Allergien
- Morphine, Sulfa
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 01.10.2021
- Impfdatum
- 03.09.2021
- Beginn
- 27.09.2021
- Tage bis Beginn
- 24,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest X-ray
Echocardiogram
Electrocardiogram
Fibrin D dimer
Full blood count
Pericarditis
Troponin
Symptomtext
9/3/21 vaccine received. 9/27/21 pt developed a CP, went to ED 9/28/21. Pt says she was told she had pericarditis. Pt was treated with Ibuprofen, Pt states she is improving as of today 10/1/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- ED did echo, D Dimer, CXR, EKG, troponin and CBC
- Aktuelle Erkrankungen
- HTN, migraine, tachycardia, peripartum cardiomyopathy,
- Vorgeschichte
- HTN, migraine, tachycardia, peripartum cardiomyopathy,
- Andere Medikamente
- Medication cyclobenzaprine 10 mg tablet take 1 tablet by oral route every bedtime as needed Flonase Allergy Relief 50 mcg/actuation nasal spray,suspension spray 1 - 2 spray by intranasal route every day in each nostril as needed hydroch
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 29.09.2021
- Impfdatum
- 09.09.2021
- Beginn
- 27.09.2021
- Tage bis Beginn
- 18,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Facial paralysis
Speech disorder
Symptomtext
Developed Bells Palsy facial dropping and difficulty speaking started on 9/22/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- -
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 13.08.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Deep vein thrombosis
Pain in extremity
Ultrasound Doppler
Symptomtext
Patient received the first dose of the COVID-19 Moderna vaccine. One week later developed left calf pain. At the time was in a boot for tendonitis. Described pain as new and aggravated by ambulation or pressure. No alleviating factors. She was sent by podiatrist for vascular study which was positive for DVT to the left distal popliteal vein and posterior tibial veins. Patient was seen at the ED and prescribed rivaroxaban.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- -
- Labordaten
- Duplex US positive for DVT on 8/21/21
- Aktuelle Erkrankungen
- Tendonitis (in walking boot), history of COVID infection in January 2021
- Vorgeschichte
- Prothrombin gene mutation (heterozygous), depression, hypothyroidism
- Andere Medikamente
- Albuterol inhaler, aspirin 81 mg, cholecalciferol, citalopram, fish oil, fluticasone nasal spray, fluticasone-salmeterol oral inhalation, levothyroxine, melatonin, multivitamin
- Allergien
- Ciprofloxacin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 24.09.2021
- Impfdatum
- 02.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure measurement
Chest discomfort
Chest pain
Dizziness
Hypotension
Influenza like illness
Myalgia
Presyncope
Symptomtext
Tightness in the chest; Chest hurt really bad; Very dizzy; blood pressure was extremely low at 95/57; Almost past out 2 times; flu like symptoms; Arm was very sore; This spontaneous case was reported by a consumer and describes the occurrence of PRESYNCOPE (Almost past out 2 times), INFLUENZA LIKE ILLNESS (flu like symptoms), CHEST DISCOMFORT (Tightness in the chest), CHEST PAIN (Chest hurt really bad) and DIZZINESS (Very dizzy) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included COVID-19 in March 2021. On 02-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Sep-2021, the patient experienced INFLUENZA LIKE ILLNESS (flu like symptoms) and MYALGIA (Arm was very sore). On 03-Sep-2021, the patient experienced PRESYNCOPE (Almost past out 2 times), CHEST DISCOMFORT (Tightness in the chest), CHEST PAIN (Chest hurt really bad), DIZZINESS (Very dizzy) and HYPOTENSION (blood pressure was extremely low at 95/57). On 04-Sep-2021, PRESYNCOPE (Almost past out 2 times), INFLUENZA LIKE ILLNESS (flu like symptoms), CHEST DISCOMFORT (Tightness in the chest), CHEST PAIN (Chest hurt really bad), DIZZINESS (Very dizzy) and HYPOTENSION (blood pressure was extremely low at 95/57) had resolved. On 06-Sep-2021, MYALGIA (Arm was very sore) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 03-Sep-2021, Blood pressure measurement: 95/57 (Low) 95/57. 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. The same day after vaccination, patient felt flu like symptoms that lasted till 04-Sep-2021 and their arm was very sore till 05 or 06Sep2021. Around 8pm on 03-Sep2-021 patient felt tightness in the chest, their chest hurt bad, patient was very dizzy and almost passed out 2 times, all these till 04Sep2021. Patient blood pressure was extremely low at 95/57 till 04-Sep-2021. Patient has no previous or current myocarditis or pericarditis diagnose. Patient had covid-19 back in March 2021, and tested positive on 29Mar2021, about 5 days after the symptoms started. Patient was not hospitalized for this and the treatment received was antibiotic and a z-pack. Caller state the covid-19 infection symptoms were mainly upper respiratory. Company comment: This case concerns a 59-year-old male patient with no relevant medical history, who experienced the unexpected non-serious event of Presyncope. The event occurred 1 day after first dose of Spikevax. The rechallenge was not applicable, as the events happened after the first dose. The benefit-risk relationship of Spikevax is not affected by this report. Case seriousness downgraded due to lack of evidence of seriousness from a regulatory or clinical standpoint according to source document.; Sender's Comments: This case concerns a 59-year-old male patient with no relevant medical history, who experienced the unexpected non-serious event of Presyncope. The event occurred 1 day after first dose of Spikevax. The rechallenge was not applicable, as the events happened after the first dose. The benefit-risk relationship of Spikevax is not affected by this report. Case seriousness downgraded due to lack of evidence of seriousness from a regulatory or clinical standpoint according to source document.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210903; Test Name: Blood pressure; Result Unstructured Data: 95/57.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: COVID-19.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 20.09.2021
- Impfdatum
- 04.08.2021
- Beginn
- 04.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Electric shock sensation
Headache
Hyperhidrosis
Myalgia
Renal pain
Sluggishness
Symptomtext
Severe all over muscle pain, concentrated mostly in the kidney area. Shooting electrical type pains in head. Sweating. Headache. Ongoing sluggishness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure, high cholesterol, a-fib
- Andere Medikamente
- D3, Zinc, Magnesium, Asprin 81mg, Eliquis 10mg, Potassium Cholride ER 8meq, HCTZ 12.25mg, Simvastatin 20mg, Losartan Potassium tab 100mg, Amlodipine besylate tab 2.5mg, Carvedilol 6.25mg
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 17.09.2021
- Impfdatum
- 16.08.2021
- Beginn
- 12.09.2021
- Tage bis Beginn
- 27,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- Confirmed by Ophthalmologist
- Aktuelle Erkrankungen
- Rheumatoid Arthritis Atrial Fib
- Vorgeschichte
- See Above
- Andere Medikamente
- warfarin metropolol methotraxate folic acid
- Allergien
- hexachlorophene
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 13.09.2021
- Impfdatum
- 06.07.2021
- Beginn
- 06.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alanine aminotransferase increased
Blood glucose
Carbon dioxide decreased
Diarrhoea
Epistaxis
Liver function test abnormal
Metabolic function test
Metabolic function test abnormal
Nausea
Thrombosis
Symptomtext
1) About 10:45am July 6, 2021 - Severe Nausea and Diahrea folowing Vaccination 2) Continued Diahrea July 7, july 8, July 9, ranging from watery stool to dark loose stool 3) july 9 at 6am - awoke with NOSEBLEED in Left Nostril, dark red blood with clots 4) July 9 about 7am, NOSEBLEED in Left Nostril, dark red blood with stringy clots 5) July 9 about 8 am NOSEBLEED in Left Nostril, bright red blood with clots 6) July 9 2pm, Was able to see Nurse Practioner at my Drs. Office who confirmed bleeding in both nostrils and ordered blood testing. 6) July 10 and July 11, continued Diahrea with Black, Dark Stool, with urgency.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- Blood Test Results Liver Function Test shows elevated ALT levels (38U/L) Basic Metabolic Panel shows HIGH GLUCOSE (106) level and LOW CARBON DIOXIDE Levels (19 mmol/L) and
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- SCIATICA
- Andere Medikamente
- 400 MG IBUPROFEN TAKEN ABOUT 12 HRS PRIOR
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 03.08.2021
- Impfdatum
- 03.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Presyncope
Symptomtext
Lightheaded, sweating, feeling faint, almost fainted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none
- Andere Medikamente
- none known
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 22.07.2021
- Impfdatum
- 20.07.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arteriogram coronary normal
C-reactive protein increased
Cardiac ventriculogram left abnormal
Catheterisation cardiac normal
Chest crushing
Chest discomfort
Chest pain
Hyperdynamic left ventricle
Myalgia
Myocarditis
Painful respiration
Pleuritic pain
Pyrexia
Red blood cell sedimentation rate increased
Troponin increased
White blood cell count increased
Symptomtext
presented to the emergency room with symptoms of chest pain. He received Moderna covid vaccine on Tuesday and since then he has been having symptoms of myalgias and chest pain. He mentions that the chest pain is substernal, gets worse with deep breaths. It gets worse when he lays on his back. And feels better when he sits up. He also had subjective fevers. When he presented to the emergency room he was having crushing chest discomfort with a troponin level at 10 and was referred for an emergent coronary angiography with concerns for acute coronary syndrome. Diagnosis/Impression: Acute myocarditis after Covid vaccination: Based on positional changes and pleuritic nature of the chest pain. Given troponin level left hand and ongoing crushing chest discomfort he was emergently taken to the Cath Lab where he does not have any significant coronary artery disease or thrombotic occlusions. LV gram shows hyperdynamic LV systolic function. At this time his symptoms are consistent with myocarditis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- 7/22/2021: WBC- 14.5, Sed Rate 25, Troponin 18.70, CRP 108.69,
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, Depression
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 21.07.2021
- Impfdatum
- 20.07.2021
- Beginn
- 20.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Flushing
Hyperhidrosis
Nausea
Paraesthesia
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Mild, Systemic: Flushed / Sweating-Medium, Systemic: Nausea-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 20.07.2021
- Impfdatum
- 20.07.2021
- Beginn
- 20.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Loss of consciousness
Symptomtext
Patient received 1st dose covid vaccine and at the 13 minute mark slumped over in chair. We promptly went out to keep him from falling and within 10 seconds he regained consciousness and was able to tell us his name, where he was and was alert. He said he was feeling very weak all over but no other symptoms. We called 911 and while paramedics were on the way he lost consciousness another 2 times each time for about 10 seconds. He was alert when paramedics arrived and they took blood sugar, blood pressure, oxygen levels and applied leads to his chest. From what I could tell all those tests came back normal. While they were evaluating him, he lost consciousness again and they were able to revive him with sternal rub. They transported the patient to the ER for further evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none that I have results from
- Aktuelle Erkrankungen
- None noted on consent form
- Vorgeschichte
- Previous throat cancer but cancer free since February
- Andere Medikamente
- none that I'm aware of
- Allergien
- None noted on consent form
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 20.07.2021
- Impfdatum
- 19.07.2021
- Beginn
- 19.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Loss of consciousness
Pallor
Symptomtext
pt passed out, yet remained sitting, we helped get him to the floor to lie him down, he was very pale and profusely sweating. He stated he had not eaten or drank anything and had worked outside as well. Took his BP which was 105/63, placed an ice pack on his back of his neck and forehead. He remained awake during all of this and was alert. Quickly regained. Had paramedics come as well to double check status.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- BP, HR
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 16.07.2021
- Impfdatum
- 16.07.2021
- Beginn
- 16.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Fall
Head injury
Hyperhidrosis
Loss of consciousness
Palpitations
Paraesthesia
Syncope
Unresponsive to stimuli
Urinary incontinence
Symptomtext
About 2 minutes after receiving vaccine patient was seated on bench outside pharmacy, fainted and fell forward onto cement floor hitting his jaw. Patient was unresponsive for about 20 seconds while being attended to. Once he regained consciousness, he was helped to sit back on bench. He was diaphoretic and claimed to have a racing heart and right hand tingling. He lost consciousness on the bench again and lost bladder control. EMS was summoned and was on scene in 5 minutes. Patient did not claim to have difficulty breathing. Pharmacist called patient about 3 hours after the event and he was still in hospital with apparent problems keeping his blood pressure adequate.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- past smoker
- Andere Medikamente
- ventolin inhaler
- Allergien
- no known drug allergies
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 10.07.2021
- Impfdatum
- 10.07.2021
- Beginn
- 10.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Nausea
Seizure
Vomiting
Symptomtext
patient was administered moderna covid 19 vaccine and with 10 minutes developed shortness of breath, nausea and vomiting, and seizures X3. ems was dispatched and patient was taken to hospital for further evaluation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- we checked patient's pulse rate and o2 saturation with a pulse oximeter. pulse was 109 and o2 sats were 100
- Aktuelle Erkrankungen
- diabetes, rheumatoid arthritis, thyroid deficiency, GERD, depression
- Vorgeschichte
- diabetes, rheumatoid arthritis, thyroid deficiency, GERD, depression
- Andere Medikamente
- none
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 30.07.2023
- Impfdatum
- 21.09.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Cardiac disorder
Cerebral disorder
Condition aggravated
Eye disorder
Impaired driving ability
Impaired work ability
Pneumonia
Ventricular extrasystoles
Symptomtext
After I took the first vaccine shot at Facility I started having issues with my heat having PVC's after I took the second shot I got pneumonia and was out of work for several days. Later I started having issues driving and found out that the shot has caused my eyes and brain not to connect so I am unable to drive up and down hills. I have been under a doctor's care since July of 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- I went to the ER at Facility and having been going to the Vision since July 2022 with my eyes.
- Aktuelle Erkrankungen
- Heart Issues
- Vorgeschichte
- Heart issues
- Andere Medikamente
- Thyroid Medication Heart Medication
- Allergien
- penicillin and sulfa drugs
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 13.07.2023
- Impfdatum
- 26.08.2021
- Beginn
- 18.04.2023
- Tage bis Beginn
- 600,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Anticoagulant therapy
Atypical pneumonia
Blood creatinine increased
COVID-19
Cardiac telemetry
Catheterisation cardiac abnormal
Chronic respiratory failure
Computerised tomogram thorax abnormal
Condition aggravated
Cough
Dry eye
Dysphagia
Dyspnoea
Echocardiogram normal
Electrocardiogram ambulatory normal
Hypophagia
Lung consolidation
Symptomtext
Patient is a 74 y.o. female with a PMH of multiple VTE's (PE and DVT) s/p Greenfield filter and remote pulmonary embolectomy at CCF maintained on anticoagulation (Xarelto), CTEPH followed by the pulmonary hypertension clinic, chronic hypoxemic respiratory failure maintained on 2 L NC, reactive airway disease, OSA (on CPAP), morbid obesity who presented from home on 4/18/2023 with shortness of breath, cough, fever, myalgias. Referred to the ED by her pulmonologist. Found to be positive for SARS-CoV-2 on admission. Initiated on dexamethasone and remdesivir. Assessment and Plan COVID-19 - Presented with: Shortness of breath, cough, fevers, myalgias - Symptom onset: 4/12/23 - Positive COVID-19: 4/17/23 - Vaccination status: Vaccinated with Moderna and boosted with Moderna with booster dose on 8/26/21 - CT Chest on admission showed: Ill-defined scattered ground-glass consolidations with a lower lobe predominance, suggestive of atypical pneumonia. Main pulmonary artery enlargement, a nonspecific finding which can be seen with pulmonary hypertension. - Oxygen status: 2 L NC (baseline) - Decadron: Yes. Expected end date 4/27/23 - Remdesivir: Yes - DVT prophylaxis: Currently on full anticoagulation - S/p 40 mg IV Lasix on 4/20 and 4/21 . Resume home Lasix on discharge Chronic hypoxemic respiratory failure - At baseline oxygen requirements of 2 L NC, continue CTEPH History of multiple VTE's (PE and DVT) status post Greenfield filter and remote pulmonary embolectomy at CCF maintained on anticoagulation (Xarelto), chronic thromboembolic pulmonary hypertension followed by the pulmonary hypertension clinic. RHC 6/20 showed improved PA pressures with mPAP 24, PVR 3.4 WU, preserved CI - Cardiology consulted on admission. Unlikely will recommend RHC this admission during acute COVD-19 infection - Continue home Xarelto, riociguiat and Opsumit as per home regimen - Pulmonology consulted (patient known to Dr.) AKI SCr 1.28 on admission; baseline ~0.7-0.8. Suspect prerenal in the setting of recent poor PO intake - Held home Lasix - S/p 1 liter LR bolus, gentle hydration - Renally-dose medications as indicated - Resolved Reactive airway disease Prior PFTs without obstruction. Maintained on Symbicort, Duonebs q6h, prn albuterol - Continue Symbicort, prn albuterol - Substitute scheduled Duonebs with Spiriva (avoid nebulizers given +COVID-19) - On Decadron for COVID-19 infection Dysphagia History of esophageal stricture - Continue daily PPI Abnormal finding on imaging CT on admission demonstrated: "Hyperattenuating foci in the right atrium are nonspecific, but consider correlation with echocardiogram to assess for right atrial thrombus." - Echocardiogram this admission unremarkable - The patient is on anticoagulation with Xarelto, continue History of tachycardia Follows with Heart and Vascular. Previous 48-hour Holter monitor did not show any sustained arrhythmias - Continue home Toprol 50 mg daily - Monitor on telemetry CAD Mild nonobstructive coronary artery disease defined by LHC in 3/2012 with subsequent negative stress testing and historically preserved LV systolic function. Most recent nuclear stress test on 3/30/23 without evidence of inducible myocardial ischemia. Follows with cardiology - Continue statin therapy OSA - Continue nocturnal CPAP (endorses compliance at home). Hospital order placed Chronic pain - Has been prescribed recent bursts of steroid per OP review Dry eyes - Continue prednisolone drops as per home regimen Morbid obesity BMI 44.62 - Encourage weight loss through aggressive lifestyle modifications
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atypical pneumonia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 11.04.2023
- Impfdatum
- 04.11.2021
- Beginn
- 08.03.2023
- Tage bis Beginn
- 489,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Angiopathy
Asthenia
Biopsy kidney abnormal
Blood creatinine increased
Blood glucose fluctuation
Colitis
Computerised tomogram abdomen abnormal
Cough
Decreased appetite
Diarrhoea
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Chronic respiratory failure
Clostridium test negative
Hypertension
Iron deficiency anaemia
Lung opacity
Symptomtext
81-year-old male patient of MD who presented with poor appetite, weakness, diarrhea and cough. He tested positive for COVID-19. His background history include CKD stage IV/V, diabetes mellitus, CAD, chronic anemia, BPH, hyperlipidemia and skin cancer. Diarrhea resolved Colitis resolving Noncontrast CT of the abdomen/pelvis with diffuse colonic thickening suggestive of colitis. In the setting of COVID-19 infection. C. difficile testing neg Loose stool is improved. He was on Zosyn, now discontinued. Imodium as needed. Covid-19 Virus Infection COVID pneumonia Chronic respiratory failure - 2L Date of onset of symptoms: 2-26-2023 Symptoms present on admission: Cough, weakness, poor appetite. Date of covid positive test: 3-8-2023 Vaccination status: 2 shots and 1 booster Imaging: CXR with left lower interstitial opacities. Current oxygen requirements: 2 liters Medical therapy: steroids stop dexamethasone Consultants following:ID Anticipated special isolation end date: 3/8/23 - d/w ID - now off Isolation. CXR on 3/8 with left lower lobe interstitial opacities suspicious for pneumonia. Repeat CXR today. . Discussed with ID. No need for further antibiotics CKD stage IV/V Had renal biopsy in 9/2022 with finding of advanced chronic changes in the setting of severe vascular disease with obliterative microvascular changes. No need for renal replacement therapy at present. Cr improved to 2.60 Nephrology following.as an OP Generalized weakness Consult PT/OT and CM Anemia of CKD and iron deficiency Follows with hematology and receives Venofer. Monitor Hb closely. HTN He has a history of left renal artery stenosis status post stent. Also history of right subclavian stenosis. BP is now higher. Repeat CXR BP remains persistently elevated. Continue Norvasc and Coreg, increase dose of lisinopril. Increasing amlodipine to 10 mg Hydralazine as needed Diabetes mellitus II Fluctuations in BG since yesterday. Likely component of IV steroid. Adjusted Lantus and SSI. Continue to monitor, avoid hypoglycemia. Chronic respiratory failure Continue O2 support and bronchodilators. He uses O2 at home. Currently on 2 L.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 15.03.2023
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Bone pain
Complex regional pain syndrome
Condition aggravated
Fibula fracture
Pain in extremity
Tibia fracture
Symptomtext
I have had Complex Regional Pain Syndrome (CRPS) for 20 years (in remission for 18 years) until a broken tibia and fibula in my left ankle/leg in the late 1990's. I have a Medtroinic Pain Pump 24/7 to deal with the pain. Following my second COVID-19 vaccine, my body interpreted the shot as an injury which it reacted to by triggering my CRPS to kick back in. In the right arm where the vaccine was given, I had tremndous pain that traveled to my right shoulder and this pain has not gone away since that vaccine on 02/11/2021. I sought medical advise about whether or Not to take the BOOSTER given my reaction to the second vaccine. It was determined that the risks of getting COVID were greater than taking the BOOSTER,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Lumber sympathetic block on 11/23/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Complex Regional Pain Syndrome; COPD
- Andere Medikamente
- -
- Allergien
- Demerol. Gabipantin, Lyrica, levo-flaxin, bee/wasp stings
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 94,0
- Geschlecht
- M
- Eingang
- 06.02.2023
- Impfdatum
- 10.11.2021
- Beginn
- 03.02.2023
- Tage bis Beginn
- 450,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Alanine aminotransferase normal
Anion gap increased
Aspartate aminotransferase increased
Bacterial test positive
Basophil count decreased
Basophil percentage decreased
Bilirubin urine
Blood albumin normal
Blood alkaline phosphatase normal
Blood bilirubin normal
Blood calcium normal
Blood chloride increased
Blood creatinine normal
Blood glucose normal
Blood lactic acid decreased
Blood pH normal
Blood potassium normal
Blood sodium normal
Symptomtext
Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on February 03, 2023 16:33 Verified By: MD on February 03, 2023 16:33 Encounter Info: Hospital, Inpatient, 02/03/23 - * Final Report * History of Present Illness/Subjective Chief complaint: Altered mental state HPI: Patient is a 95-year-old male patient with history of atrial fibrillation not on anticoagulation, dementia, history of stroke in adulthood, hyperlipidemia, incomplete bladder emptying, chronic urinary tract infections, obstructive sleep apnea and bladder Contracted presented to emergency department via EMS from extended-care facility for altered mental status. History was obtained from daughter who was at bedside and this history is from emergency room chart due to patient's altered mental state which is quite altered from his baseline dementia. Patient was apparently recently discharged from our facility on January 28 where he had been treated for flu. At that time patient was septic septic from influenza a. As per the reports from family patient has gotten progressively worse since and has been out of it for past 3 days. Patient also complains of having cough which is blamed on influenza A infection recently. Patient has never used oxygen at home and apparently was having low oxygen today when he presented to the emergency room as low as 87% on room air. Upon evaluation in the emergency room laboratory data was fairly benign with normal white count normal kidney function glucose elevated at 120 normal liver enzymes troponin at 27 BNP 45 lactate 1.6 urinalysis showing large amount of hemoglobin positive nitrites many bacteria flu negative COVID-positive patient was not COVID-positive at his last hospitalization. A chest x-ray was obtained that failed to show any pneumonia and CT abdomen pelvis was done that showed no acute findings in the abdomen or pelvis chronic findings which remain unchanged CT head without IV contrast shows advanced microvascular ischemic changes and generalized atrophy if clinical suspicion for acute ischemia persists consider further evaluation with brain MRI no CT evidence of acute intracranial hemorrhage. Patient is full code which has been confirmed with the family by emergency room doctor. Since patient was requiring oxygen it was decided to bring inpatient for treatment of COVID. Review of Systems All 13 point review of systems were reviewed with the patient and are negative except as specified in the HPI Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) None reported this timeframe Patient Weight Patient Height None Reported General: Alert but not oriented Eye: Pupils are equal, round and reactive to light HEENT: Normocephalic Neck: Supple, normal range of motion Oropharynx: No erythema or drainage. Respiratory: Lungs are clear to auscultation. Cardiovascular: Normal rate, Regular rhythm. Gastrointestinal: Soft, Non-tender. Musculoskeletal: Normal range of motion, No focal tenderness Integumentary: Warm, Dry, No rash Neurologic: No focal weakness. Sensation intact. Normal mood and affect Assessment/Plan 1. COVID U07.1 New diagnosis of COVID 19 likely acquired from nursing home. -We will start patient on remdesivir since symptoms are fairly new and patient is requiring oxygen. -Dexamethasone 6 mg IV daily -Check procalcitonin levels and other appropriate labs as ordered in order set. -Oxygen as needed. -Keep patient isolated. 2. Hypoxia R09.02 Oxygen as above -Hypoxia resulting from COVID-19 infection. 3. Altered mental state R41.82 Altered mental status likely due to current infection by COVID-19 and hypoxia. -Oxygen as needed. -Monitor for falls. 4. Dementia F03.90 Noted. 5. Recurrent UTI N39.0 Patient will be given ceftriaxone for his urinary tract infection and we will look for cultures and if cultures are negative we will discontinue antibiotics. He may just be having colonization due to having recurrent urinary tract infections and incomplete bladder emptying. Urine cultures from last visit were negative but 1 urine cultures from January 14 showed ESBL positive E. coli. -We will treat with cefepime 6. Atrial fibrillation I48.91 Patient is rate controlled on atenolol. -I do not see any anticoagulation for this patient likely due to advanced age and risk of falls. -Continue to monitor for now. 7. BPH with obstruction/lower urinary tract symptoms N40.1 Noted resume home medications 8. GERD (gastroesophageal reflux disease) K21.9 Patient will be on Protonix. 9. Hyperlipemia, mixed E78.2 Resume home medications Orders: acetaminophen, 650 mg, Orally, Tablet, Q4H, PRN, Pain, Mild PO (1-3 out of 10)/Fever, 02/03/23 15:59:00 albuterol, 2.5 mg, Neb Inhal, Inhalation SOLN, Aerosol Treatment, Q4H, PRN, Shortness of Breath/Wheezing, 02/03/23 15:59:00, RT Care Assessment and Protocol per Policy labetalol, 10 mg, IV Push, Injection, Q6H, PRN, Systolic Blood Pressure, 02/03/23 15:59:00 ondansetron, 4 mg, IV Push, Injection, Q6H, PRN, Nausea/Vomiting IV - Use First, 02/03/23 15:59:00 polyethylene glycol 3350, 17 GM, Orally, Powder, Daily, 02/04/23 9:00:00 promethazine, 12.5 mg, IVPB, Injection, Q6H, PRN, Nausea/Vomiting IV - Use First, 02/03/23 15:59:00, 300 mL/hr, Infuse Over 10 minutes, Total Volume (mL) = 50 Sodium Chloride 0.9% 1,000 mL, Total Volume (mL) = 1,000, IV, 02/03/23 15:59:00, 60 mL/hr, Clinical Weight 2000 mg Sodium, 20 gm Saturated Fat Diet Admit to Inpatient Basic Metabolic Panel Call Blood Glucose Call Diastolic Blood Pressure Call Heart Rate Call Mental Status Changes Call O2 Saturation Call Oxygen Need Greater Than Call Respiratory Distress Call Respiratory Rate Call Systolic Blood Pressure Call Temperature CBC w/Differential CK SerPl QN Comp Metabolic Panel CRP SerPl QN D-Dimer Pl QN Ferritin SerPl QN Fibrinogen Initiate IV Care Protocols As Appropriate Initiate Mobility Protocol Initiate Skin and Wound Care Protocol L pneumophila Ag Ur QL LDH SerPl QN Level of Care Magnesium SerPl QN Medical Service OT Evaluation and Treatment Phosphorus SerPl QN Procalcitonin PT Evaluation and Treatment Resuscitation Status Strep pneumoniae Ag Urine Troponin-I High Sensitivity Vital Signs Weight Code Status None Recorded Chronic Problem List Atherosclerosis of native artery of right lower extremity with rest pain Atrial fibrillation Balanoposthitis Bladder neck contracture BPH with obstruction/lower urinary tract symptoms Cholelithiasis Chronic UTI Colon polyps Critical lower limb ischemia Dementia Dysuria Exudative age-related macular degeneration of left eye with active choroidal neovascularization GERD (gastroesophageal reflux disease) History of stroke in adulthood Hyperlipemia, mixed Incomplete bladder emptying Lumbosacral disc disease Malnutrition Neurogenic bladder OSA (obstructive sleep apnea) Osteoarthritis Psoriasis PVC (premature ventricular contraction) Recurrent UTI Spondylolisthesis Tobacco use Urinary retention Procedure/Surgical History ?TURP (11/2018) ?Rt knee peroneal nerve release (07/22/2015) ?Bone density scan (06/24/2014) ?Colonoscopy (12/18/2012) ?Rt TKA (2000) ?Colonoscopy ?Dental implants ?EGD- bleeding ulcer with clamp ?Hemorroid surgery ?Inguinal Hernia Repair Surgical History Internal 09/11/2019 Bladder Neck Repair MD 11/28/2018 TUR Prostate MD 07/22/2015 Nerve Repair Peroneal (Right) MD Medications Home Medications (15) Active aspirin 325 mg oral delayed release tablet 325 mg = 1 Tablet, Orally, Daily atenolol 25 mg oral tablet 0.5 Tablet, Orally, BID cetirizine 10 mg oral tablet 10 mg = 1 Tablet, PRN, Orally, QAM Cranberry oral capsule 300 mg, Orally, BID finasteride 5 mg oral tablet See Instructions, Take 1 tablet by mouth once daily lactobacillus acidophilus oral capsule 1 Capsule, Orally, Daily miconazole 2% topical powder 1 App, Topical, BID, to affected area mirtazapine 7.5 mg oral tablet 7.5 mg = 1 Tablet, Orally, At Bedtime Misc Supplement See Instructions, Australian Dream Cream for his back, uses PRN family sts it is an antihistamine and has herbs. From Pharmacy multivitamin Multiple Vitamins oral tablet 1 Tablet, Orally, Daily omeprazole 20 mg oral delayed release capsule 1 Capsule, Orally, Daily polyethylene glycol 3350 oral powder for reconstitution 17 GM, Orally, Daily pravastatin 40 mg oral tablet See Instructions, TAKE 1 TABLET BY MOUTH AT BEDTIME PreserVision AREDS 2 1 Capsule, Orally, BID triamcinolone 0.1% topical cream 1 App, Topical, TID, apply a thin film Active Scheduled Inpatient Medications Sodium Chloride 0.9% 1,000 mL IV 60 mL/hr One-Time Medications Given 02/02/23 00:00:00 TO 02/03/23 16:33:54 None Reported PRN Medications (0600 - 0559) from 02/02 - 02/03 None Reported Allergies Restoril (Difficulty Breathing) codeine (breathing difficulty, Vomiting) lovastatin (weakness) Social History Alcohol Current, Daily Electronic Cigarette/Vaping E-Cigarette Use Never. Home/Environment Lives with Spouse. Living situation: Home with assistance. Home equipment: Walker/Cane. Family/Friends available for support: Yes. Major illness in household: Yes. Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History High blood pressure..: Father. Stroke: Father. Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 7.8 k/cumm (02/03/23 10:23:00) RBC: 4.87 million/cumm (02/03/23 10:23:00) Hgb: 14.6 GM/dL (02/03/23 10:23:00) Hct: 45 % (02/03/23 10:23:00) MCV: 92 fL (02/03/23 10:23:00) MCH: 29.9 pg (02/03/23 10:23:00) MCHC: 32.4 GM/dL (02/03/23 10:23:00) RDW: 14.4 % (02/03/23 10:23:00) Platelet: 323 k/cumm (02/03/23 10:23:00) MPV: 8.4 fL (02/03/23 10:23:00) Neutrophils %: 66 % (02/03/23 10:23:00) Lymphocytes %: 19 % (02/03/23 10:23:00) Monocytes %: 15 % (02/03/23 10:23:00) Eosinophils %: 0 % (02/03/23 10:23:00) Basophils %: 0 % (02/03/23 10:23:00) Absolute Neutrophil: 5.1 k/cumm (02/03/23 10:23:00) Absolute Lymphocyte: 1.4 k/cumm (02/03/23 10:23:00) Absolute Monocyte: 1.1 k/cumm (02/03/23 10:23:00) Absolute Eosinophil: 0 k/cumm (02/03/23 10:23:00) Absolute Basophil: 0 k/cumm (02/03/23 10:23:00) Chemistry: Sodium SerPl QN: 144 mmol/L (02/03/23 10:23:00) Potassium SerPl QN: 4 mmol/L (02/03/23 10:23:00) Chloride SerPl QN: 108 mmol/L (02/03/23 10:23:00) Carbon Dioxide SerPl QN: 23 mmol/L (02/03/23 10:23:00) Anion Gap: 13 mmol/L High (02/03/23 10:23:00) BUN SerPl QN: 19 mg/dL (02/03/23 10:23:00) Creatinine SerPl QN: 0.81 mg/dL (02/03/23 10:23:00) Estimated GFR (CKD-EPI, no race): 81 mL/min/1.73m2 (02/03/23 10:23:00) Estimated CRCL (CG): 58 mL/min Low (02/03/23 10:23:00) Glucose SerPl QN: 120 mg/dL High (02/03/23 10:23:00) Calcium Total SerPl QN: 9.6 mg/dL (02/03/23 10:23:00) Alkaline Phos SerPl QN: 65 Units/L (02/03/23 10:23:00) ALT SerPl QN: 24 Units/L (02/03/23 10:23:00) AST SerPl QN: 49 Units/L High (02/03/23 10:23:00) Bilirubin Total SerPl QN: 0.4 mg/dL (02/03/23 10:23:00) Total Protein SerPl QN: 7.7 GM/dL (02/03/23 10:23:00) Albumin SerPl QN: 3.7 GM/dL (02/03/23 10:23:00) Lipase SerPl QN: 39 Units/L (02/03/23 10:23:00) Troponin-I High Sensitivity: 27 ng/L High (02/03/23 10:23:00) BNP Pl QN: 45 pg/mL (02/03/23 10:23:00) Lactate Venous Pl QN: 1.6 mmol/L (02/03/23 10:23:00) pH Bld Venous QN: 7.37 (02/03/23 10:23:00) PCO2 Bld Venous QN: 47 mmHg (02/03/23 10:23:00) PO2 Bld Venous QN: 71 mmHg High (02/03/23 10:23:00) Base Excess Bld Venous: 1 mmol/L (02/03/23 10:23:00) Bicarb Bld Venous Calc: 27 mmol/L (02/03/23 10:23:00) O2 Sat Bld Venous Calc: 94 % (02/03/23 10:23:00) Patient Temperature: 37 DegC (02/03/23 10:23:00) Urine Studies: Color: Yellow (02/03/23 10:34:00) Clarity: Clear (02/03/23 10:34:00) Specific Gravity: >=1.030 (02/03/23 10:34:00) pH: 6.0 (02/03/23 10:34:00) Protein: 30 Abnormal (02/03/23 10:34:00) Glucose: NEGATIVE (02/03/23 10:34:00) Ketones: NEGATIVE (02/03/23 10:34:00) Bilirubin: NEGATIVE (02/03/23 10:34:00) Hgb Ur: LARGE. Abnormal (02/03/23 10:34:00) Nitrite: POSITIVE Abnormal (02/03/23 10:34:00) Urobilinogen: NormalUro (02/03/23 10:34:00) Leukocyte Esterase Ur: NEGATIVE (02/03/23 10:34:00) WBC: 6-10 Abnormal (02/03/23 10:34:00) RBC: 11-20 Abnormal (02/03/23 10:34:00) Bacteria: Many Abnormal (02/03/23 10:34:00) Squamous Epithelial: Few (02/03/23 10:34:00) All Other Labs: COVID 19 Specimen Source: Nasopharyngeal (02/03/23 10:34:00) Coronavirus SARS-CoV2 Rapid: Detected Abnormal (02/03/23 10:34:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (02/03/23 10:34:00) Rapid Influenza A PCR: Not Detected (02/03/23 10:34:00) Rapid Influenza B PCR: Not Detected (02/03/23 10:34:00) Diagnostics Radiology Results - Last 24 hours Across Visits 02/03/2023 10:54 - XR Chest PA or AP Portable IMPRESSION:1. No acute findings in the chest.Thank you for consulting our team of subspecialty radiologists at Radiology. Please contact us with any questions. 02/03/2023 11:32 - CT Abd/Pelvis W/IV Contrast IMPRESSION:1. No acute findings in the abdomen or pelvis.2. Chronic findings as described.Thank you for consulting our team of subspecialty radiologists at Radiology. Please contact us with any questions. 02/03/2023 11:32 - CT Head W/o IV Contrast IMPRESSION: 1. Advanced microvascular ischemic changes and generalized atrophy.If clinical suspicion for acute ischemia persists, consider furtherevaluation with brain MR.2. No CT evidence of acute intracranial hemorrhage.Thank you for consulting our team of subspecialty neuroradiologists at Radiology. Health careproviders wishing to discuss this case further can contact the Neuroradiology Reading Room. Signature Line Electronically Signed on 02/03/23 16:33 ________________________________________________________ MD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Molecular Diagnostic Tests COVID 19 Specimen Source Nasopharyngeal Coronavirus SARS-CoV2 Rapid * (A) Detected Microbiology Studies - Bacterial Urine CX (+) POS In Progress Bacterial L pneumo Urine Ag QL Not Detected L pneumo Urine Ag QL Interp L pneumo Urine Ag QL Interp Strep pneumo Ag Ur Not Detected Strep pneumo Ag Ur Interp Negative Viral FS Rapid Influenza Method PCR - Liat Rapid Influenza A PCR * Not Detected Rapid Influenza B PCR * Not Detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 11.01.2023
- Impfdatum
- 01.12.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 31,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Bronchitis
Chest pain
Chills
Dyspnoea
Fatigue
Headache
Nausea
Oropharyngeal pain
Pain
Respiratory tract congestion
Sinusitis
X-ray abnormal
Symptomtext
Chills, body aches, chest conjestion/pain, fatigue, sore throat, headache, nausea ,short of breath Sinusitis, bronchitis ,asthma shortness of breath. Now using nebulizer albuterolsul 2.5 mg/3 prn , wixela 2 x Da
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Urgent Care had an X Ray, diagnosed sinusitisand bronchitis at Urgent Care ( practice Manager) to a Asthma Dr, To a Ear, Nose and Throat Dr. Short of breath and called 911 they evaluated
- Aktuelle Erkrankungen
- Chronic pelvic bad cramps bone deterioration, rt hip, back pain Chronic sinus , nasal mucus, always cold
- Vorgeschichte
- CABG Asthma, HTN, vertebrobasilar artery syn Mixed hyperlipidemia , sinus
- Andere Medikamente
- Winelands 500-50 1 puff am and pm Oxybutynin 5mg 3x da Lisinopril 20 mg 2x da Atenolol 50 mg 1 xda Amlodipine 10mg 1x da Fluticisone prop 50 nadal 2 ea nostril Aspirin 80 mg 1 x da Cerrizine hcl 10mg 1 x da Albuterol hfa prn 2 puffs q 4-6 h
- Allergien
- Sulfur, iodine iv dye Pcn, dairy, shellfish
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 18.11.2022
- Impfdatum
- 20.11.2021
- Beginn
- 17.11.2022
- Tage bis Beginn
- 362,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fall
Mobility decreased
SARS-CoV-2 test positive
Symptomtext
Patient had a fall and was on the floor for approx one day. Tested positive for covid on hospital admission. Treatment includes supportive care with benzonatate, robitussin, and pulmonary toilet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 30.09.2022
- Impfdatum
- 02.09.2021
- Beginn
- 07.10.2021
- Tage bis Beginn
- 35,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Hypoaesthesia
Limb discomfort
Paraesthesia
Sensory disturbance
Symptomtext
I chose my left arm for the vaccine because I heard it would leave the arm sore for a while and i use my right arm. After getting the 1st vaccine a week later my right arm started tingling and feeling kind of weird. I ignored it and went on to get the 2nd vaccine. Around a week after that vaccine i noticed the same feeling in my right arm but it was more intense. The feeling it gives off is like my arm is asleep but it is the most uncomfortable feeling ever. It starts pretty much from the right side of my face all the way down to my finger tips. The arm feels heavy at times, numb and tingly at times, and harm to rest on anything or hold up. This is an everyday thing now. It did go away for months and months but somehow has come back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- NO test have been done but it has been mentioned to my primary care doctor several times.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 16.08.2022
- Impfdatum
- 13.09.2021
- Beginn
- 17.09.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Blood lactic acid increased
Blood test
Computerised tomogram normal
Condition aggravated
Headache
Intervertebral disc degeneration
Migraine
Occipital neuralgia
Psoriasis
Seborrhoeic dermatitis
Sinus headache
Sinusitis
Spinal X-ray abnormal
White blood cell count increased
X-ray abnormal
Symptomtext
On 09/17/2021, 3 days after receiving my third dose of Moderna, I had a sinus infection. I went to my family doctor who referred me to an allergy specialist who I saw on October 5th. I had x-rays done October 11th. I was then referred to a neurologist. On October 26th, I saw a doctor for back pain. I had x-rays done in the beginning of November. They found some degenerative issues and diagnosed degenerative disc disease. November 16th, I received dose 2 of my Shingles vaccine, which triggered a severe headache. On November 20th, I went to an urgent care clinic at my local hospital because my headaches had gotten so bad and was given prednisone. December 16th, I was finally able to see a neurologist who diagnosed me with multiple forms of chronic headaches: Migraines, Occipital Neuralgia, and sinus headaches. I'm taking magnesium, riboflavin, and baclofen for the headaches. The headaches have subsided with the medication. The Occipital headache is still there constantly but has gotten better with the medication. On 01/03/2022, I went to see a dermatologist for the psoriasis and seborrheic dermatitis which I already suffer from but had gotten worse. I didn't have it on my face before and at that point it had spread to my face. The dermatologist prescribed ketoconazole shampoo and cream which has helped the issue. 02/02/2022 I saw my rheumatologist due to increased joint pain and fatigue and ended up doubling my dosage of HUMIRA which I now take weekly as opposed to biweekly. On 02/14/2022, I received my fourth dose of Moderna. Things, health wise, were quiet until 06/24/2022 when I ended up in the emergency room for severe vomiting where they discovered that my platelets had been increasing severely over time and were at over 700,000 per micro liter of blood. They referred me to a hematologist who I saw 08/08/2022. I am scheduled for blood tests tomorrow on 08/17/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 10/11/2021 cat scan of sinuses-nothing found; 11/2021-x-rays degenerative disc diagnosis; 06/24/2022 blood panel, high white blood cell count-hi lactate in the blood
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Psoriatic Arthritis; Chronic Headaches; Thrombocytosis
- Andere Medikamente
- HUMIRA; ZYRTEC; FLONASE; LEXAPRO; azelastine; betamethasone cream
- Allergien
- Latex; walnuts; acetaminophen
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 04.01.2022
- Beginn
- 10.05.2022
- Tage bis Beginn
- 126,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Amnesia
Anxiety
Aphasia
COVID-19
Chills
Contusion
Depression
Feeling abnormal
Irritability
Mood altered
Nausea
Neuropathy peripheral
Oedema
Pain
Paraesthesia
Rash macular
Salt craving
Symptomtext
I got COVID-19. I had chills for about 3 days then I had brain fog and memory loss and difficulty finding words. I went to the doctor and they said had paresthesia and neuropathy in arms and legs and it was intense pain. I also had nausea and upset stomach. I had bruising splotchy skin. I had salt cravings, edema, and I and a mood shift. I was anxious, irritable, and depressed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Musculoskeletal injuries
- Andere Medikamente
- Adderall XR; Ambien ER; Lexapro
- Allergien
- Sulpha Drugs
- Vorherige Impfungen
- Shingles
- Staat
- -
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 20.06.2022
- Impfdatum
- 18.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Blood test
Dysstasia
Hypoaesthesia
Injected limb mobility decreased
Injection site pain
Nerve conduction studies
Pain
Pain in extremity
Paraesthesia
Peripheral swelling
Symptomtext
Approx. 4 days after receiving the 4th Moderna vaccine (booster), patient began experiencing significant left arm pain, swollen left hand, numbness in his hand, continued pain at the injection site, could not raise left arm above his shoulder. He also started experiencing numbness and tingling in both legs, shooting pains down both legs, and difficulty getting up after sitting. Prior to this patient was very active (exercising, yard-work, traveling)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- - Patient went to his Primary Care Doctor to discuss these symptoms, and his Primary Care said "it sounds like you need more exercise" - Patient then went to another Physician to discuss his hand symptoms, and he wanted a nerve conduction test performed in his hand - Nerve conduction test was performed on 5/18/22 - When these results were discussed with this doctor on 6/10/22, he wanted more follow up based on a Physical Exam. He ordered bloodwork and wants a nerve conduction test performed on his back and legs. This will be on 7/5/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- COPD, High BP, High Cholesterol, Sick sinus syndrome (has a pacemaker)
- Andere Medikamente
- Medications for GERD, high cholesterol, high bloodpressure, Multi-vitamin, Fish Oil, Aspirin, Saw Palmetto, Vitamin C
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 24.05.2022
- Impfdatum
- 19.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Atrial fibrillation
Blood test
Cardiac monitoring abnormal
Echocardiogram abnormal
Electrocardiogram abnormal
Heart rate irregular
Palpitations
Symptomtext
I started getting that feeling that my heart was racing and the erratic heartbeat. It would come and go for 2-3 weeks. I noticed it was positional and I would notice it more at night when I was lying down at night or in the morning and it would happen during the course of the day as well. I was thinking that it would go away, but it just stayed. I was scheduled for a procedure for my bladder. On April 13, I went in for the that procedure and was going to get a filler and they put me on a heart monitor, and I was having a fib, at 110-140 beats per minute and spiking at 150-160. The surgeon said he wouldn't do the surgery with a fib. They said I needed to go to the ER, and I was discharged on 4/15 from the hospital. They did an EKG and echocardiogram. They diagnosed me with A fib and scheduled me with a doctor. They also put me on medication in the hospital and didn't release me until the heart rate was down to regular rate. I was put on metoprolol 50mg twice daily. They also put me on blood thinner Eliquis 5mg twice daily as well. I went to see the doctor and he did a cardiogram and I'm still in a fib but he suggested having a cardioversion. He told me to think about it. I'm on the medication and I have a follow up in 6 months. He said I can decide when I want to get this procedure done and to follow up if I don't want to, or if it gets worse. I'm still in a fib but I can still do whatever I was doing prior to this event according to the doctor. From the doctor at the hospital and from the other doctor as well, both indicated that my heart did look healthy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- 2,0
- Labordaten
- EKG-indicated a fib; Echocardiogram-indicated a fib; Cardiogram-indicated a fib; Blood work
- Aktuelle Erkrankungen
- COVID towards the beginning of January of 2022
- Vorgeschichte
- Bladder incontinence; Cycle of Upper Respiratory Infections at least once a year
- Andere Medikamente
- Oxybutynin 10mg OTC Aleve as needed
- Allergien
- Sensitivities to pain medication PERCOCET, etc.
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 21.05.2022
- Impfdatum
- 15.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 16,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chest X-ray normal
Laboratory test normal
Magnetic resonance imaging spinal normal
Mobility decreased
Pain
Pain in extremity
X-ray limb normal
Symptomtext
Ever since I got the booster shot I have had unrelenting pain in all of my joints. I have pain in my wrists, elbows, fingers, knees, and ankles and random shooting pains in other parts of my body. Every time I go to a Dr. and mention this new pain since I got the booster nobody listens to me. Every morning I wake up like monster. I can't even bend my limps for several minutes. This is horrible. I will never, ever get another booster or Covid shot .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Xray of hands and chest May, 2022 MRI cervical spine May, 2022 Labs done in Dr. office March 2022 / results normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- NECK STINOSIS
- Andere Medikamente
- Benicar 40/12.5 mg Vyvanse 40 mg Duloxetine DR 60 mg Acyclovir 400 mg
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 20.05.2022
- Impfdatum
- 01.10.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 73,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Arrhythmia
Blood test
Cardiac ablation
Cardiac stress test
Dizziness
Electrocardiogram
Heart rate irregular
Magnetic resonance imaging heart
Ventricular extrasystoles
Symptomtext
Dec 13 th irregular heart beat d. with PVCs. Never had this arrhythmia before no history of high blood pressure. Dizzy and lightheaded periods of feeling faint .Medications to treat were no successful due to reaction to medication. May 17 2022 had successful cardiac ablation
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- 1,0
- Labordaten
- Stress test, cardiac MRI, blood work , EKG and Cardiac ablation
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma and GERD Sleep apnea
- Andere Medikamente
- Ventolin inhaler Qvar inhaler as needed Vit D Singular daily
- Allergien
- Narcotics and anesthesia
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 24.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Pain
Symptomtext
I have a lot of aches and pains and I noticed it a little bit more than normal the next day. Also, I have COPD and I noticed it was harder to breath when I laid down.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetic Type 2; COPD; High Cholesterol
- Andere Medikamente
- Tramadol; Lovastatin; Metformin; Albuterol; Generic Antihistamine
- Allergien
- I had a reaction to a Z-pak once.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 11.03.2022
- Impfdatum
- 26.10.2021
- Beginn
- 15.01.2022
- Tage bis Beginn
- 81,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Discomfort
Fatigue
Feeling abnormal
Mobility decreased
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I developed a sore throat in mid Jan 2022 accompanied with fatigue and discomfort. After a week, I took a self-test and tested positive. At that point I was feeling really bad. I went to the Health Clinic and received an anti-body drug. I was in bed for a week with a fever, dry cough, fatigue and soreness. After another two weeks I began to feel like I was back to normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Synthroid, Atorvastatin, Adoctripine, Exaltapine, Zaleplon
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 22.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal distension
Anxiety
Decreased appetite
Panic attack
Tachyphrenia
Tremor
Symptomtext
Panic attack; Body shaky; Mind is racing; Stomach in knots; Lot of anxiety; Does not want to eat; This spontaneous case was reported by a consumer and describes the occurrence of PANIC ATTACK (Panic attack), TREMOR (Body shaky), TACHYPHRENIA (Mind is racing), ABDOMINAL DISTENSION (Stomach in knots) and ANXIETY (Lot of anxiety) in a 53-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 22-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Jul-2021, the patient experienced PANIC ATTACK (Panic attack), TREMOR (Body shaky), TACHYPHRENIA (Mind is racing), ABDOMINAL DISTENSION (Stomach in knots), ANXIETY (Lot of anxiety) and DECREASED APPETITE (Does not want to eat). At the time of the report, PANIC ATTACK (Panic attack), TREMOR (Body shaky), TACHYPHRENIA (Mind is racing), ABDOMINAL DISTENSION (Stomach in knots), ANXIETY (Lot of anxiety) and DECREASED APPETITE (Does not want to eat) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant product use was provided by the reporter. No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 25.02.2022
- Impfdatum
- 29.10.2021
- Beginn
- 19.02.2022
- Tage bis Beginn
- 113,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chest pain
Cough
Dyspnoea
Oropharyngeal pain
Pain
Pulmonary congestion
Pyrexia
Respiratory symptom
Symptomtext
ADMITTED W/ SORE THROAD, CHEST CONGESTION/PAIN, DRY COUGH, FEVERS, BODY ACHES, URI SYMPTOMS, SOB, GENERALIZED WEAKNESS FOR 3 DAYS PTA.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- COPD, POLYSUBSTANCE USE, CHRONIC PAIN, SCHIZOAFFECTIVE DISORDER, HTN, PERIPHERAL NEUROPATHY
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discomfort
Hypersensitivity
Mouth swelling
Paraesthesia
Injection site pain
Joint range of motion decreased
Lip swelling
Muscle spasms
Musculoskeletal stiffness
Myositis
Neck pain
Pain
Symptomtext
Patient called the clinic around 10 minutes after receiving her vaccine to report that she was driving back because she was experiencing symptoms of an allergic reaction. Clinic staff readied an emergency bag and evaluated whether patient should head to the emergency room. When patient arrived back at clinic, she described tingling and heaviness in her face and some swelling in her mouth. She was given Benadryl and water and seated in the observation area for 30 minutes. Patient then reported feeling better and drove herself home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Strawberries
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 14.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Palpitations
Symptomtext
Heart palpitations, chest pain approximately one week from receiving booster. Made worse when laying down. Sent to ER by Urgent Care clinic
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Kyleena
- Allergien
- Sulfa antibiotics and PCN
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Back pain
Computerised tomogram thorax abnormal
Fatigue
Injection site pain
Lymphadenopathy
Musculoskeletal chest pain
Musculoskeletal pain
Pain in extremity
Pericardial effusion
Pericardial fibrosis
Symptomtext
Sore arm, fatigue, pain at shoulder blade, rib cage , and back on the right side, pain in left shoulder at injection site, pericardial thickening, vs a trace pericardial effusion (fluid and inflation around heart), mildly enlarged lymph node
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Musculoskeletal chest pain
- Hospital-Tage
- -
- Labordaten
- CT scan without contrast of chest
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure, Type 2 diabetes, High cholesterol (under control with medicine), Anxiety
- Andere Medikamente
- Losartan 50 mg 2x daily, Carvedilol 12.5 mg 2x daily, Glipzide 10mg 3x daily, Zescipa 1 g 2x daily, Alprazolpam 1 mg 3x daily or as needed, Vitamin D 50,000 mg 2x weekly, Amalodapine 1x daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest X-ray
Chest pain
Electrocardiogram
Laboratory test
Myalgia
Symptomtext
patient reports having muscle aches. also with left-sided chest pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- presented for evaluation 12/9/2021. labs, EKG and chest xray ordered
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- dyslipidemia, hypertension, history of hepatitis b
- Andere Medikamente
- losartan, rouvastatin
- Allergien
- lisinopril, simvastatin, trazodone
- Vorherige Impfungen
- history of muscle aches after 1st and 2nd dose of moderna covid vaccinations
- Staat
- OH
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 06.12.2021
- Impfdatum
- 31.10.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 30,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Herpes zoster
Paraesthesia
Rash vesicular
Symptomtext
Roughly 30 days after receiving a booster shot of Moderna mRNA COVID 19 vaccine, I developed shingles in the T10 dermatome on the right. Symptoms were at first slow to develop and included change in sensation of the skin the in the affected area, followed several days later by a blistering rash with vesicles in a very dermatomal distribution. My primary care physician confirmed the diagnosis of shingles. I am an otherwise healthy 37yo male with no medical problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Primary care visit on 12/3/2021.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Mens Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 18.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Exposure during pregnancy
Hot flush
Joint range of motion decreased
Pain in extremity
Tinnitus
Tremor
Symptomtext
28 weeks pregnant Arm so sore I cannot move, along with chills causing shaking uncontrollably and hot flashes. Hearing ringing or whispering around 10pm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Injection site pain
Pain in extremity
Paraesthesia
Symptomtext
When the nurse gave me the injection, I felt it go down the nerve in my arm. I assumed the pain would go away, but it has not. It hurts all of the time from my elbow and down into my hand and sometimes it hurts up my arm and into my shoulder. There is also a tingle similar to my hand and arm being "asleep" most of the time. In the past couple of days I have also had the feeling of numbness in my hand.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- On 11/11/21 I emailed my PC doctor to see if this was a normal reaction since any pain from my past 2 shots went away fairly quickly. She told me to make an appointment since it was not getting better. I could not get an appointment with her, so I saw one of her partners on 11/12/21. He said it was the nerves in my arm and has referred me to Neurology. I have an appointment with Neurology on December 6, 2021 for further evaluation.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- high blood pressure, obese
- Andere Medikamente
- hydrochlorothiazide 25 mg tablet
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 19.10.2021
- Beginn
- 20.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure fluctuation
Hypertension
Symptomtext
Patient states fluctuating high blood pressure after vaccination. Patient stated typical blood pressure did not exceed 130/90 prior to vaccination, but since vaccination has stated that his blood pressure is routinely elevated up to 170's/90's.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Tachycardia
Symptomtext
Pt has hx of heart transplant and is followed by Clinic Pt experienced tachycardia post COVID-19 third dose requiring hospitalization. Patient reported this to our office post hospitalization.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- Unknown. Pt reported she was seen at Clinic for adverse reaction of tachycardia and was hospitalized and reported this to our office post hospitalization.
- Aktuelle Erkrankungen
- Pt has hx of heart transplant and followed by Clinic. All questions regarding patient's medical conditions, allergies, treatment, medications, routine vaccinations should be requested from Clinic.
- Vorgeschichte
- Pt has hx of heart transplant and followed by Clinic. All questions regarding patient's medical conditions, allergies, treatment, medications, routine vaccinations should be requested from Clinic.
- Andere Medikamente
- Clinic has this information.
- Allergien
- Pt has hx of heart transplant and followed by Clinic. All questions regarding patient's medical conditions, allergies, treatment, medications, routine vaccinations should be requested from Clinic.
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 07.11.2021
- Impfdatum
- 23.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Dyspnoea
Fatigue
Hypertension
Irritable bowel syndrome
Pain in extremity
Pyrexia
Symptomtext
Fever of 100 for 2 days/nights. Soreness in left arm. Persistent shortness of breath and fatigue after minor exertions since the vaccination. Telehealth visit on 10/22/2021 with HCP. She recommended C/D/Zinc supplement, but this makes my IBS and BPH worse. She also said exercise could help. Symptoms have not gotten worse but have not improved either.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- IBS and BPH.
- Andere Medikamente
- Tadalafil 5mg
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 04.10.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood thyroid stimulating hormone
Cardiac flutter
Dyspnoea
Palpitations
Symptomtext
Palpitations, fluttering, shortness of breath for 7 days
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Cardiologist only ordered a TSH blood test on 10/11/2021, drawn on 10/12/2021
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Atrial septal defect, secundum; Aortic valve insufficiency; Bicuspid aortic valve
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 28.09.2021
- Impfdatum
- 30.07.2021
- Beginn
- 31.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adverse reaction
Dyskinesia
Influenza like illness
Migraine
Muscle twitching
Myoclonus
Symptomtext
About an hour after my first vaccine, I had an excruciating migraine (took tylenol). Around 3 am (12 hours after vaccine), I woke up with flu like symptoms and began to have myoclonic jerks. I had full body "twitches" for four plus hours. I would have a jerk/twitch 4-5 times in a minute. For example, my right leg would jerk, then my arm, then my neck, etc. It was not a whole body twitch, it was different parts of my body one after another.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Prior to my vaccination, I had CBC, TSH and cholesterol blood drawn. I met with physician after my vaccine and adverse reactions occurred to discuss what happened. My physician was worried I had a neurological adverse reaction. He requested me to do further research, meet with neurologist and infectious disease physicians.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- zoloft
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 23.09.2021
- Impfdatum
- 10.09.2021
- Beginn
- 10.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood cholesterol increased
Dizziness
Drug screen negative
Dyspnoea
Full blood count abnormal
Hypertension
Palpitations
Paraesthesia
Sexually transmitted disease test
Vaccination complication
Vitamin D decreased
Symptomtext
Within five minutes I suffered an adverse reaction to the vaccine. I experienced heart palpitations, high blood pressure, dizziness, shortness of breath, and tingling sensation in my hands. Lasted approximately 2 hours.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- A complete bloodwork was conducted on me. Results only showed low on vitamin D and slightly high cholesterol. Everything else was normal. Drug screen was negative as well as STDs.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- Codeine. Adverse reaction, diaphragm goes into spasms.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 23.09.2021
- Impfdatum
- 20.09.2021
- Beginn
- 21.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Fear
Panic attack
Sleep disorder
Swollen tongue
Symptomtext
Panic attack induced by throat, soft pallet, tongue swelling causing shortness of breath and inability to sleep due to fear. Did take aspirin and ibuprofen to attempt to reduce swelling and monitored for approximately 12 hours before feeling relief
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- sleep apnea not properly treated and possible tooth infection, also untreated tinnitus in left ear
- Vorgeschichte
- Anxiety, sleep apnea, left ear tinnitus
- Andere Medikamente
- Sporadic use of Paroxetine HCL 20MG prescription for 2x daily, but do not have health insurance so still using same bottle filled 03/21/2021 by taking approximately half tablet per day, sometimes half tablet every other day
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 17.09.2021
- Impfdatum
- 02.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Dizziness
Hypotension
Influenza like illness
Injection site pain
Symptomtext
Flu like symptoms, soreness at injection sight, chest pains and tightness in chest, dizziness, blood pressure was extremely low, almost passed out twice
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Valsartan 160mg (once daily)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 16.09.2021
- Beginn
- 16.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Erythema
Feeling abnormal
Heart rate increased
Palpitations
Rash macular
Symptomtext
Patient drove to clinic at 1400 and received vaccine at 1410. Patient was instructed to wait in her vehicle for 15 minutes and to honk if she needed medical care. At 1420, patient comes out of car and walks to vaccine table to alert nurses that she felt ?like her heart was racing and I feel spacey?. Patient was sat down and vitals were taken. Vitals appeared within normal limits. Patient?s cheeks and chest were red and splotchy. Patient given cold water and was instructed to wait with nurse for an additional 30 minutes. Patient continued to have complaints of racing heart and lightheadedness. Vitals taken again and pulse increased from 100s to 120s. EMS called and arrived at 1450. EMS took vitals and patient?s heart rate was increasing to 130s. EMS took patient by ambulance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- 1420 vitals: 141/79, pulse: 99, RR: 18, O2: 100 1445 vitals: 145/75, pulse: 120, RR: 18, O2:100 1450 vitals: 138/70, pulse: 130, RR: 18, 02:100
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- Adult asthma
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 15.09.2021
- Impfdatum
- 15.09.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Paraesthesia oral
Pruritus
Symptomtext
After receiving vaccine, patient reported an "odd feeling" in her tongue and itching all over.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- osteoporosis, neuropathy, chronic pain syndrome, bipolar disorder, fibromyalgia
- Andere Medikamente
- singulair, gabapentin, hydrocodone, xolair, estradiol
- Allergien
- penicillin, azithromycin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 11.09.2021
- Impfdatum
- 10.09.2021
- Beginn
- 10.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure decreased
Cough
Dizziness
Dyspnoea
Hypoaesthesia
Paraesthesia
Peripheral coldness
Somnolence
Visual impairment
Symptomtext
Drop in blood pressure, trouble breathing, cough, numb and tingling cold hands, headache, seeing black spots, feeling light headed. Started a few minutes after vaccination, needed to sit with feet elevated, lasted an hour and needed with falling asleep like narcoleptic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None. I self-treated and waited, nearly used epi-pen.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma, allergies, eczema, possible mcas, chronic Lyme, h. Pylori
- Andere Medikamente
- Nystatin, singulair, Zyrtec, ketotifen, nac, vitamins, probiotics, citrus line, ornithine, yucca, xopenex inhaler as needed, Flovent as needed, chromodynamics sodium nebulizer as needed, black seed oil, molybdenum, PEA, ox bile, nad+.
- Allergien
- Sulfa, erythromycin, Zithromax, legumes, dairy, wheat/gluten, hemp, pumpkin, buckwheat, cilantro
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 01.09.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Eye pruritus
Eye swelling
Injection site mass
Symptomtext
Following vaccination patient experienced itching and swelling of her eyes which she self treated with antihistamines. The following day she developed a large lump at the site of injection . Today she called complaining of unusual sternum pain .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- -
- Andere Medikamente
- none
- Allergien
- penicillins
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 03.09.2021
- Impfdatum
- 03.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Erythema
Symptomtext
The Patient presented to our pharmacy after making an appointment for a booster dose of her Moderna vaccine. The patient stated they had a compromised immune system and their last dose was administered on 2/8/21. Consistent with the law we administered a booster for the patient. Within several minutes the patient's face became red and they stated they had difficulty breathing. it was at this moment I as the pharmacist made used my clinical judgement to administer an Epipen dose to the patient. I asked my staff call emergency services. within moments their face came back to normal coloring and they were able to breath better. they did state their heartbeat was racing consistent with administration of the Epipen. I remained with the patient and counseled to focus on breathing. emergency services arrived several minutes later and took the patient in the ambulance with them. they then went to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Patient has a "compromised immune system". she was unable to verify which one.
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 02.09.2021
- Impfdatum
- 01.09.2021
- Beginn
- 02.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Hypoaesthesia
Paraesthesia
Vaginal haemorrhage
Symptomtext
- Vaginal bleeding started about 0600 on 09/02/2021; not menstrual bleeding. Consistency and color not typical of my monthly menstrual bleeding. Currently monitoring. - Also experiencing mild joint pain (elbow, wrist) in injection arm - started evening of vaccination date (9/1/21) and not yet resolved; experienced mild numbness and tingling in hand on injection arm early morning of 09/02/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Pre-natal vitamins by VitaFusion.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 25.08.2021
- Impfdatum
- 25.08.2021
- Beginn
- 25.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Hypopnoea
Nausea
Respiratory rate increased
Tremor
Symptomtext
? 9:37AM ? 2nd dose of Moderna vaccine administered IM into right arm ? Patient waited 15 minutes for observation ? 9:52 AM - Patient checked out with technician at 9:52AM and reported nausea and trembling ? 9:53 AM ? BP was measured 176/90mmHg ? 10:01 AM ? BP reassessed 151/94mmHg; Patient reported that symptoms did not improve so 10mL of diphenhydramine 12.5mg/5mL (total 25mg) administered to patient and emergency number was called. Continued to observe patient. ? 10:06AM ? Patient reported difficulty breathing and no improvement in symptoms. Observed rapid shallowing breathing, so 1 dose (0.3mg) of epinephrine auto-injector was administered IM into left outer thigh ? ~10:08-10:15AM ? Ambulance arrived, reported incident to paramedics, and patient was taken to hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Prediabetic
- Vorgeschichte
- None reported
- Andere Medikamente
- Zquil
- Allergien
- Amoxicillin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 17.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Nausea
Pain
Pyrexia
Tremor
Symptomtext
9 hours after the shot I got a fever , my body started shaking uncontrollably, my whole body hurt everywhere , I was nauseated and dizzy .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 15.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Arthralgia
Dizziness
Dyspnoea
Headache
Lip swelling
Myalgia
Pain
Pruritus
Pyrexia
Rash
Tongue ulceration
Wheezing
Symptomtext
patient had high fever a few hours later (about 4 hours after shot) and it lasted for 24 hours+, severe headache, body aches (muscle and joints), SOB and wheezing on 8/14 for which she used rescue inhaler, bumps on right shoulder, itchy arms, woke up 8/15 lips double size, tongue ulcerated and swollen - today 8/15 is dizzy, has been taking Benadryl and prescribed oral steroid therapy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- chicken pox vaccine
- Staat
- AL
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 17.07.2021
- Impfdatum
- 17.07.2021
- Beginn
- 17.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Heart rate increased
Hypoaesthesia oral
Symptomtext
Patient administered First Dose Covid Vaccine. 10 minutes into observation period, patient states she is having shortness of breath, increased heart rate, tongue numbness, and lip and mouth numbness. RPH Administered 25mg of liquid bendaryl to patient and called 911 for EMS/Paramedics. Patient was taken on stretcher to ER with father. Patient was alert and able to respond/talk to staff/paramedics at time of departure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- n/a
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 12.07.2021
- Impfdatum
- 12.07.2021
- Beginn
- 12.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Paraesthesia
Paraesthesia oral
Symptomtext
PATIENT REPORTED FEELING A TINGLING SENSATION ON SKIN WITHIN 1 HOUR OF RECEIVING SHOT -- SENSATION MAY HAVE DEVELOPED TOWARD END OF ONSITE OBSERVATION PERIOD BUT PATIENT BELIEVED IT WAS GOOSEBUMPS FROM A/C. PATIENT REPORTED THAT OVER THE NEXT HOUR (BY APPROXIMATELY 12:30PM) SHE HAD FULL-BODY ITCHING INCLUDING TONGUE AND IMMEDIATELY WENT TO URGENT CARE. SHE WAS GIVEN A STEROID INJECTION AND SUPPLIED WITH DIPHENHYDRAMINE WHICH CONTROLLED HER REACTION. SHE HAS BEEN ADVISED THAT SHE NEEDS TO KEEP LIQUID DIPHENHYDRAMINE ON HAND AND WATCH FOR ANY RETURN OF SYMPTOMS OVER THE NEXT SEVERAL DAYS, AND IF SYMPTOMS RETURN TAKE BENADRYL IMMEDIATELY AND SEEK IMMEDIATE EMERGENT CARE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- NONE REPORTED TO US
- Aktuelle Erkrankungen
- EPILEPSY (CONTROLLED ON LAMICTAL)
- Vorgeschichte
- EPILEPSY
- Andere Medikamente
- LAMICTAL
- Allergien
- NSAIDS CARBAPLATIN IMITREX
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 09.07.2021
- Impfdatum
- 09.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea exertional
Ear pain
Headache
Hypoaesthesia
Hypoaesthesia oral
Pruritus
Respiratory tract congestion
Symptomtext
Shortly after patient recieved vaccine she started complaing about itching in the lower forarm area on the same side of the vaccination site. a few hours later I called patient to check on her and she informed me that she had started to get numbness in her tongue and lower face, she had congestion and a headache and felt like when she was walking ar doing things around the house that her breathing was labered. she also stated that he had pain in her (R) ear for about an hour
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- lantanoprost
- Allergien
- Tetanous, quinolones, oxycodone, tetracyclines, morphine, sulfa, penicillins
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 11.04.2023
- Impfdatum
- 13.09.2022
- Beginn
- 24.03.2023
- Tage bis Beginn
- 192,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dizziness
Fatigue
Headache
Pyrexia
SARS-CoV-2 test positive
Sacroiliac joint dysfunction
Symptomtext
Tested positive for Covid - 19 on March 24, 2023. Cough, Sore throat, head ache, fever, tiredness Tested negative with BinaxNow Test on 3/31/2023 Still have coughing , headache and or light-headedness, and sore throat occassionaly during each day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- OnGo Home test tested positive 3/24/2023 Tested negative with BinaxNow Test on 3/31/2023
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- GERDS
- Andere Medikamente
- Pantoprozole Sodium 40 mg twice a day, Calcium 600 mg D3 20 mcg
- Allergien
- Demerol
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 14.02.2023
- Impfdatum
- 13.07.2022
- Beginn
- 03.01.2023
- Tage bis Beginn
- 174,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bacterial translocation
Blood culture negative
COVID-19
Cholecystitis chronic
Cyst
Diarrhoea
Escherichia bacteraemia
Fatigue
Infection
Influenza
Leukocytosis
Nausea
Pyrexia
SARS-CoV-2 test positive
Sepsis
Vomiting
Symptomtext
Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note: "69 year old female with a history of ESRD on HD secondary to PCKD, paroxymal Afib, hypertension, hyperlipidemia, hypothyroidism, and seizure disorder who presented to facility on 1/2/23 with a two week history of nausea, vomiting, diarrhea, and fatigue. During the hospitalization she was found to be septic with fever and a leukocytosis. She was found to have COVID-19, Influenza A, and an Escherichia coli bacteremia. She was started on IV Ceftriaxone while workup began to investigate the etiology behind the the bacteremia. Patient has many sources of infection: GI translocation vs chronic cholecystitis vs infected cyst. ID was consulted - believe the source of infection is related to chronic cholecystitis. Patient was recommended in the past to have a cholecystectomy done at a tertiary care center, but patient refused. This time patient continues to resist surgery, as she does not believe the operation will prolong her overall prognosis as it relates to PCKD. She would like to forgo surgery at this time. Repeat blood cultures were drawn and were negative for 48 years - she will be discharge on (renally-dosed) Ciprofloxacin 500 mg daily with instructions to complete a 14-day course of antibiotics. "
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- 4,0
- Labordaten
- Covid PCR detected. 01/02/2023
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Cardiovascular Hypertension Paroxysmal atrial fibrillation Digestive Intractable nausea and vomiting Polycystic liver disease Biliary dyskinesia Choledocholithiasis on MRCP Acute pancreatitis without infection or necrosis Perforation of the intestines GERD (gastroesophageal reflux disease) Endocrine Hypothyroid Hypoparathyroidism Urinary ESRD on dialysis Gross hematuria Dysuria Acute cystitis AKI (acute kidney injury) Other Seizure disorder (*) Hypocalcemia Abdominal pain, generalized Anemia of chronic disease Hyperphosphatemia Metabolic acidosis with increased anion gap and accumulation of organic acids Metabolic encephalopathy Palliative care encounter Right upper quadrant abdominal pain SIRS (systemic inflammatory response syndrome) Chronic back pain
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet Take 2 tablets by mouth every 6 (six) hours as needed for Pain. amLODIPine (NORVASC) 10 MG tablet Take 1 tablet by mouth every morning. apixaban (ELIQUIS) 2.5 mg tab tablet Take 1 tablet by mouth 2 (two
- Allergien
- CodeineNausea Only Statins-hmg-coa Reductase InhibitorsMuscle Symptoms Keflex [Cephalexin]Hives, Itching, Rash
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 01.11.2022
- Impfdatum
- 21.09.2021
- Beginn
- 01.04.2022
- Tage bis Beginn
- 192,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fibrosis
Pain
Symptomtext
fibrocystic lump that did not go away. he thought ut will go away but started paining for last 2 weeks
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- no
- Allergien
- no
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 01.11.2022
- Impfdatum
- 27.04.2022
- Beginn
- 11.08.2022
- Tage bis Beginn
- 106,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
COVID-19
Chills
Headache
Myalgia
Nasal congestion
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
Started on Aug. 11 at 3:00a.m. Woke up with plugged up head and terrible headache. Took a home Covid test and tested positive for Covid. Called pulmonologist that morning and he wanted me on Paxlovid. I called my doctor and she called in a prescription for Paxlovid. Started it on the 12th of August. I did a home rest every other day and they were positive until Aug. 16 when it was negative. I tested negative every other day for 8 days. My symptoms were an extremely congested head and a headache. I also had chills but no fever. Sore muscles and joints and a sore throat. I never did get a cough. Was able to work in yard and do the usual things I have to do. Rested as much as possible.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Just did home tests and took Paxlovid.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- COPD
- Andere Medikamente
- Calcium, Vit.D, daily multivitamin, probiotic, Anoro Ellipta inhaler
- Allergien
- Hydrocodone
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 17.10.2022
- Impfdatum
- 21.09.2021
- Beginn
- 21.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Vomiting
Symptomtext
Vomiting x4 times, headache. Given Tylenol 650mg and Zofran 4mg x1. PT went home to rest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 14.10.2022
- Impfdatum
- 08.10.2022
- Beginn
- 09.10.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Herpes zoster
Pain
Rash
Sensitive skin
Symptomtext
Rashes developed on chest one day after the Modern bivalent Covid booster shot. Doctor confirmed shingles due to reduced immunity. All symptoms of shingles developed after the doctor visit including clusters of rashes on one side of upper body, painful blisters filled with liquid, sensitive skin, stabbing pain etc. Now on medication, Valacyclovir 1 gm, for the fourth day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Shingles diagnosis on 10/14/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Birth control pill (Camilla)
- Allergien
- None
- Vorherige Impfungen
- Fever.
- Staat
- MI
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 09.08.2022
- Impfdatum
- 06.10.2021
- Beginn
- 10.01.2022
- Tage bis Beginn
- 96,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Abdominal pain upper
Alanine aminotransferase increased
Arteriogram coronary abnormal
Aspartate aminotransferase increased
Back pain
Bilirubin conjugated increased
Blood albumin decreased
Blood alkaline phosphatase increased
Blood bilirubin increased
Blood ethanol
Blood iron decreased
Blood lactic acid
C-reactive protein increased
COVID-19
Chest X-ray normal
Haemoglobin decreased
Laboratory test
Symptomtext
Pt presented to the ED on 1/10 with CC of abdominal pain. Pt was seen in ED a month ago for similar abd pain and had CTA that showed endovascular leak. Pt was discharged home at that point. Pt having RUQ pain radiating to his back. Pain is sharp, stabbing. He reported it was the worse pain he ever had. Has had cholecystectomy in 5/2020. He reported some N/V with this. In ED pt with VS of temp of 98, heart rate 69, respiration rate 18, blood pressure 132/72, and sats 97% on room air. Labs with hemoglobin low at 12.4, albumin low at 3.0, direct bilirubin elevated at 3.0, total bilirubin elevated at 3.6 alk-phos elevated at 292, AST elevated at 251, ALT elevated at 420, lipase of 36, lactate is 0.7, CRP elevated at 6.67, iron level low at 32, serum ethanol level less than 3, UA negative, COVID-19 PCR positive . Ultrasound abdomen was negative. MRCP with no evidence of biliary obstruction or compelling evidence of hepatic parenchymal disease. A left simple renal cysts noted. Pt was placed in observation. He got 1 L of normal saline, thiamine IV, Solu-Medrol IV, Dilaudid IV, and IV benadryl. GI was consulted and ordered MRCP that was negative for any choledocholithiasis. Recommended follow up in 2-4 weeks to discuss endoscopy. Felt abdominal pain may be related to COVID as well. As COVID 19 test came back positive pt was admitted for further workup. Troponin x 3 negative. CXR with no acute process.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 2,0
- Labordaten
- See above
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 02/09/2021 Abdominal aortic aneurysm (AAA) without rupture 1996 MI (myocardial infarction) Date Unknown Arthritis Date Unknown Barrett's esophagus Date Unknown CAD (coronary artery disease) Date Unknown Gastrointestinal disorder Date Unknown GERD (gastroesophageal reflux disease) Date Unknown Heart disease Date Unknown HTN (hypertension) Date Unknown Hyperlipidemia Date Unknown Sensory disorder
- Andere Medikamente
- aspirin (HALFPRIN) 81 MG tablet ferrous sulfate (FEOSOL, 65 FE,) 325 (65 FE) MG tablet gabapentin (NEURONTIN) 300 MG capsule losartan (COZAAR) 50 MG tablet metoprolol succinate (TOPROL XL) 25 MG SR tablets omega-3 fatty acids (FISH OIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 03.05.2022
- Beginn
- 31.05.2022
- Tage bis Beginn
- 28,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Fatigue
Headache
Malaise
Nasal congestion
Pain
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Symptomtext
Covid symptoms started on 05/31/2022 with nasal stuffiness and congestion, and that was the biggest symptom apart from a slight headache that I thought was from a lack of caffeine. Last night I had a little fatigue and I still have the nasal congestion and sneezing but other than that I feel pretty good. I am still waiting on the PCR results but home test showed positive. I think by tomorrow I will feel better. I was a bit fatigued and a bit achy but not much.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Covid Positive 05/31/22
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Cholesterol, Sleep Apnea
- Andere Medikamente
- Crestor, Vitamin D, Zyrtec
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 25.04.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 11,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pityriasis rosea
Rash
Skin lesion
Symptomtext
Booster shot was administered on 4/25/2022 at 10:45 am. Rash occurred on 5/6/2022. Initially an annular lesion appeared on the left forearm (Harold Patch). The rash then spread to the arms, neck, chest, back, abdomen, and upper thighs. The rash consisted of oval lesions following the lines of cleavage. The diagnosis is Pityriasis Rosea. Patient was misdiagnosed by her PCP and given a Medrol dose pack prior to her visit at my Dermatology office on 5/19/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Blood test to rule out syphilis was ordered.
- Aktuelle Erkrankungen
- No illnesses
- Vorgeschichte
- No chronic illnesses or long-standing health conditions
- Andere Medikamente
- vitamin D3, black elderberry, Alive Multivitamin
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 16.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood urine present
Chromaturia
Computerised tomogram
Fatigue
Headache
Pain
Urine analysis abnormal
Symptomtext
After 24 hours after getting booster I started getting fatigue, headache, aches and pains in shoulders, arms, upper legs, and fever. I had to take off work then the next day my urine was dark and a reddish color. I went to the doctor get urine tested and it tested positive for blood in urine. Urine blood went day in 3 days. And that's still an ongoing issue since I got COVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Urine test, CT scan, UTI test.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Tri-Estarylla
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 22.10.2021
- Beginn
- 18.04.2022
- Tage bis Beginn
- 178,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Headache
Malaise
Oropharyngeal pain
SARS-CoV-2 test positive
Sinus congestion
Symptomtext
COVID-19 symptoms started on 04/18/22, tested positive the same day with home test. First symptom was sore throat and that was followed by a mild headache and then congestion. The congestion was limited to my head and it didn't extend to my lungs at all. Then, the sore throat diminished and the headache got to be severe and the congestion continued. I called the Doctor and she ordered Paxlovid which I started taking on April 19. I took the full course of the Paxlovid and by the time it was finished after 5 days I was feeling pretty much normal. I never had a cough, shortness of breath, muscle weakness, or extra pains. The major symptoms were the congestion and the headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- COVID-19 04/18/22 Positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Grave's Disease ITP
- Andere Medikamente
- Levothyroxine 80 mcg dose
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 27.10.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 52,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anti-cyclic citrullinated peptide antibody negative
Antibody test negative
Arthralgia
Burning sensation
Dry eye
Dry skin
Ear pain
Erythema
Exercise tolerance decreased
Eye pain
Fatigue
Hepatitis B test negative
Hepatitis C test negative
Laboratory test
Nail disorder
Red blood cell sedimentation rate normal
Rheumatoid arthritis
Rheumatoid factor negative
Symptomtext
Joint pain involving all joints, burning sensation in my feet and toes, dry eyes causing pain and blurred vision, large oozing sores on the face that dry to red, flaky areas over 24-48 hours, fatigue, decreased exercise tolerance, left ear pain, fingernails ripping. Had seen my primary care Dr. 12-23-21 and started Medrol Pak. Saw rheumatologist Dr. 2/24/22 and 4/8/22. Planning to see eye doctor, Dr. in May and Dr. again in June. Given a diagnosis of Rheumatoid arthritis with lupus-like characteristics and possibility of Sjogren's as well. Have been treated with a course of Prednisone for 7 wks without relief, given a shot of kenalog 60mg 4/8/22, now on hydroxychloroquine for 3 wks. Skin symptoms have mostly resolved since early March. Joint pain is still present but reduced after Kenalog injection. Dry eye symptoms are unchanged. Many of these symptoms had been present in milder forms prior to receiving the vaccine. I just happened to get a big flare up since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- 2/24/22-U/A-wnl, hand x-ray (Norgaard views)-wnl, labs: ANA (1.1, had been 3.82 in 2018), Rheumatoid factor (neg, had been above 33 in past), CCP (15.6), Hep B &C (neg), SS-A/Ro & SS-B/La (neg), CH50 (51), ESR (11).
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Arthritis; sciatica
- Andere Medikamente
- Acetaminophen; Diphenhydramine; Fluticasone; Cyclobenzaprine
- Allergien
- NSAIDS; Lyrica; Ethynil estradiol; Norgestimate; bee stings
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 16.03.2022
- Impfdatum
- 07.09.2021
- Beginn
- 11.01.2022
- Tage bis Beginn
- 126,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Cough
Influenza virus test negative
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I went to the ER at Clinic where I had the kidney transplant done on August 6, 2021. In January 2022 I had caught COVID. I had a fever, runny nose, and a cough. I had the monoclonal antibody infusion on January 14, 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- COVID test- positive (January 12, 2022); Flu Test- negative
- Aktuelle Erkrankungen
- Kidney Transplant
- Vorgeschichte
- Kidney Transplant; Breast Cancer
- Andere Medikamente
- Tacrolimus 3mg 2xday, CoQ 10 200mg, Nifedipine 30mg 2xday, Sulfamethoxazole-Trimethoprim 400mg, Prednisone 10mg, Pantoprazole 40mg, Multivitamin, Mycophenolate 250mg 6xday, Letrozole 2.5mg, Allopurinol 100mg 2xday, Aspirin 81mg, Carvedilol
- Allergien
- Some statin medications; Percocet; Levofloxacin
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 03.03.2022
- Impfdatum
- 01.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 14,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
I had rashes all over my body. It started just only at night then it keep getting worst. I went my doctor because it was not getting any better. He prescribed me medicine to take for it. It is getting a little better now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 09.07.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Headache
Nodule
Pain in extremity
Pyrexia
Symptomtext
A knot on her one arm; Achy arm; Fever; Headache; This spontaneous case was reported by a consumer and describes the occurrence of NODULE (A knot on her one arm), PAIN IN EXTREMITY (Achy arm), PYREXIA (Fever) and HEADACHE (Headache) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 006D21A and 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 06-Aug-2021, the patient experienced NODULE (A knot on her one arm), PAIN IN EXTREMITY (Achy arm), PYREXIA (Fever) and HEADACHE (Headache). The patient was treated with PARACETAMOL (TYLENOL) at a dose of 1 dosage form. At the time of the report, NODULE (A knot on her one arm), PAIN IN EXTREMITY (Achy arm), PYREXIA (Fever) and HEADACHE (Headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 06-Aug-2021, Body temperature: 106 f (High) 106 F. Concomitant- A medication for migraine This case was linked to MOD21-128456 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210806; Test Name: Body temperature; Result Unstructured Data: 106 F
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 25.07.2021
- Beginn
- 26.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Hypokinesia
Neck pain
Pain in extremity
Symptomtext
Pain on the Left arm, entire upper back , legs, and both side of the neck; Can not move neck to the left or right/"The vaccine Paralyzed my neck"; Pain on the Left arm, entire upper back , legs, and both side of the neck; Pain on the Left arm, entire upper back , legs, and both side of the neck; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Pain on the Left arm, entire upper back , legs, and both side of the neck), HYPOKINESIA (Can not move neck to the left or right/"The vaccine Paralyzed my neck"), BACK PAIN (Pain on the Left arm, entire upper back , legs, and both side of the neck) and NECK PAIN (Pain on the Left arm, entire upper back , legs, and both side of the neck) in a 44-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 26-Jul-2021, the patient experienced PAIN IN EXTREMITY (Pain on the Left arm, entire upper back , legs, and both side of the neck), HYPOKINESIA (Can not move neck to the left or right/"The vaccine Paralyzed my neck"), BACK PAIN (Pain on the Left arm, entire upper back , legs, and both side of the neck) and NECK PAIN (Pain on the Left arm, entire upper back , legs, and both side of the neck). The patient was treated with IBUPROFEN at an unspecified dose and frequency. At the time of the report, PAIN IN EXTREMITY (Pain on the Left arm, entire upper back , legs, and both side of the neck), HYPOKINESIA (Can not move neck to the left or right/"The vaccine Paralyzed my neck"), BACK PAIN (Pain on the Left arm, entire upper back , legs, and both side of the neck) and NECK PAIN (Pain on the Left arm, entire upper back , legs, and both side of the neck) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medication was provided. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 11.07.2021
- Beginn
- 12.06.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Oral herpes
Symptomtext
sore right arm; cold sore on her lips; This spontaneous case was reported by a consumer and describes the occurrence of MYALGIA (sore right arm) and ORAL HERPES (cold sore on her lips) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. Concomitant products included METOPROLOL and CYANOCOBALAMIN (VITAMIN B12 [CYANOCOBALAMIN]) for an unknown indication. On 11-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Jun-2021, the patient experienced MYALGIA (sore right arm) and ORAL HERPES (cold sore on her lips). At the time of the report, MYALGIA (sore right arm) and ORAL HERPES (cold sore on her lips) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment Applied Abreva Cream
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- METOPROLOL; VITAMIN B12 [CYANOCOBALAMIN]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 29.10.2021
- Beginn
- 27.12.2021
- Tage bis Beginn
- 59,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Exposure during pregnancy
Malaise
SARS-CoV-2 test positive
Symptomtext
Patient presented to labor and delivery unit on 12/28/2021 for treatment with COVID-19 monoclonal antibodies due to testing positive for COVID-19 infection on 12/27/2021 and experiencing symptoms. She was 29 weeks pregnant at presentation. During infusion, patient experience an anaphylactic response to the infusion and was kept for observation. Patient's status improved and she was able to be discharged home on 12/29/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- 1,0
- Labordaten
- COVID-19 PCR test positive on 12/27/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Anemia, polycystic ovarian syndrome
- Andere Medikamente
- Aspirin, pantoprazole, prenatal vitamin
- Allergien
- Bamlanivimab/etesevimab
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 29.12.2020
- Beginn
- 30.12.2020
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Headache
Laboratory test
Lymph node pain
Lymphadenitis
Lymphadenopathy
Pain in extremity
Skin warm
Symptomtext
Within 24 hours, had headache and was dizzy. Arm was hot to touch and sore. Within 48 hours, swollen lymph nodes started. Lymph nodes were inflamed, and the size of a lemon after the 1st dose. PCP recommended benadryl prior to the second dose to prevent unpleasant reaction; swollen lymph nodes still occurred. Same for the booster/3rd dose. All swelling had taken at least 3 months to resolve after each booster. The first time, antibiotics were prescribed by PCP. It has been abuot 2 months since the booster, and lymph nodes are still incredibly swollen and sore. PCP is not sure what else to do, except an ultrasound to see why lymph nodes are swollen and will not go down to normal size.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- labs multiple times for each dose. If booster dose not resolve, will then need ultrasound to closely examine the lymph nodes.
- Aktuelle Erkrankungen
- none, just reaction to vaccine.
- Vorgeschichte
- none known
- Andere Medikamente
- multivitamin (daily.)
- Allergien
- latex
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 12.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blood test
Chest X-ray
Cough
Eye pruritus
Feeling abnormal
Influenza virus test
Lacrimation increased
Malaise
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test
Sinus congestion
Symptomtext
I Woke Up and I Felt Achy All Over, My Eyes Were Watery & Itchy, I Had A Fever Of 101.2, I Felt Awful So I Stayed In Bed All Day. I Took Tylenol & I Noticed My Sinuses Were Feeling Really Stuffy & My Eyes Were Watery. I Kept A Low Grade Fever For The Next Few Days & Then I Started Feeling Sinusey I Was Getting Real Congested & I Had Started To Cough A Lot, I Went To Work Monday & I Was Coughing So Bad I Had To Go Home. I Called My Dr. & He Told Me To Go Home & Get Some Rest. By Monday Night I Was Really Feeling Sick. I Was Told I Should Be Feeling Better By Wednesday But I Was Actually Feeling Worse. I Had No Energy I'm Still Really Congested & I Still Cough Often. I Have An Inhaler Now That I Use When Needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- COVID-19 TEST, FLU TEST, CHEST X-RAY, BLOODWORK.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HIGH BLOOD PRESSURE, ARTHRITIS, OBSTRUCTIVE SLEEP APNEA
- Andere Medikamente
- HYZAAR, METOPROLOL TARTRATE, CRESTOR, ASPIRIN, ESTROGEN PATCH, ALEVE
- Allergien
- EGGS, VASOTEC, DEMEROL, INFLUENZA VACCINE, ADULT TETANUS
- Vorherige Impfungen
- INFLUENZA VACCINE.
- Staat
- WV
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 01.02.2022
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Incorrect dose administered
Pain in extremity
Symptomtext
Patient received the immunocompromised dose of Moderna COVID vaccine at 0.5 mL, instead of the standard 0.25 mL (patient is not severely immunocompromised as currently defined by the CDC). Pt reported that he had a sore arm and felt slightly worn down the next day. After this, patient reports no adverse reactions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Barrett's esophagus body mass index 30+ - obesity chronic obstructive lung disease complaining of erectile dysfunction coronary arteriosclerosis depressive disorder eczema essential hypertension gastro-esophageal reflux disease with esophagitis hiatal hernia history of operative procedure on shoulder hyperlipidemia multiple nodules of lung polyp of colon vitamin D deficiency
- Vorgeschichte
- Barrett's esophagus body mass index 30+ - obesity chronic obstructive lung disease complaining of erectile dysfunction coronary arteriosclerosis depressive disorder eczema essential hypertension gastro-esophageal reflux disease with esophagitis hiatal hernia history of operative procedure on shoulder hyperlipidemia multiple nodules of lung polyp of colon vitamin D deficiency
- Andere Medikamente
- albuterol sulfate Aspir-81 atorvastatin Atrovent HFA Dulera lisinopril-hydrochlorothiazide metoprolol tartrate nitroglycerin Symbicort
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 28.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anti-thyroid antibody
Anti-thyroid antibody increased
Arthralgia
Autoimmune thyroiditis
Lethargy
Myalgia
Somnolence
Temperature intolerance
Symptomtext
Diagnosed with Hashimoto's Disease - treatment is to stay on levothyroxine and continue to monitor levels - symptoms are joint pain, lethargy, sleepiness, muscle aches, sensitive to cold
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Blood tests: Thyroid Peroxidase (TPO) - 167 - previous result of 17 on 05/25/18 Thyroglobulin Antibody - 406
- Aktuelle Erkrankungen
- Type 1 Diabetes
- Vorgeschichte
- Type 1 Diabetes
- Andere Medikamente
- Lyumjev, Medroxyprogesterone, Levothyroxine, Atorvastatin, Valsartan/HCTZ, Potassium Cl, Calcium, Magnesium, Zyrtec, Flonase, Omeprazole
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 03.11.2021
- Beginn
- 13.01.2022
- Tage bis Beginn
- 71,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Headache
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I was on a mission trip and started having achiness, sore throat, severe headache, fever and cough. On Jan 12 & 13. I took home test and it was positive. On the 15th I got tested and it was positive. On, the 17th I traveled home, with a letter stating I could with an N95 mask. On the 18th when I was back home, I took another in home test and it was positive. On the 19th my symptoms began to get better. However, I still have a cough. Though a lingering cough is not unusual for me. I only took Tylenol. On Dec 15th I received Hep B and Typhoid vaccinations so I could go on my mission trip.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Covid test 3x - positive
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Hypothyroidism, High Blood pressure
- Andere Medikamente
- Losartan 150/12.5mg daily PM, Levothyroxine 1.37mcg daily AM, Tylenol 500mg prn every 3 hours
- Allergien
- Penicillin, Anti-inflammatories
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 09.12.2021
- Beginn
- 19.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Antinuclear antibody negative
Blood thyroid stimulating hormone normal
Full blood count normal
Pruritus
Rash
Thyroxine normal
Urticaria
Symptomtext
Full body hives and rash developed that required me to seek urgent care 5 times in the span of a week, and required a high dose of antihistamines and prednisone to manage symptoms. Nearly one month later, still dealing with suppressing the extremely itchy hives although not as bad as before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- CBC-normal ANA-negative/normal TSH-slightly high at 4.7 T4-normal (Never have had any allergy, rash, or hives before).
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- N/A
- Andere Medikamente
- Ortho-cyclen birth control, spironolactone-100 mg/day, Fluoxetine-20 mg/day, Adderall 10/mg as-needed
- Allergien
- Probable Pramoxine allergy.
- Vorherige Impfungen
- Swollen, red and inflamed, extremely painful arm after 1st Moderna shot
- Staat
- PA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 16.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Lymphadenopathy
Pain in extremity
Peripheral swelling
Symptomtext
Approx 2 days after receiving the vaccine patient reports that her left arm became very reddened, swollen, and painful. She also states she had swelling of her left axillary lymph nodes. Symptoms resolved over a period of 7-10 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 08.01.2022
- Impfdatum
- 24.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antinuclear antibody
Blood thyroid stimulating hormone
Differential white blood cell count
Dysphagia
Erythema
Full blood count
Mechanical urticaria
Metabolic function test
Oesophageal disorder
Pruritus
Rash
Urinary tract infection
Urine analysis
Urticaria
Symptomtext
1 week post 1/2 booster dose of moderna I developed a full body rash. Initially focused in ?hot areas? of the body (thighs, underarms, scalp, neck) In the acute phase this was extremely itchy and anywhere I scratched would develop raised welts. Treated myself with Benadryl and hydrocortisone cr?me with little improvement. I also developed esophageal tightness and a feeling like food is stuck. This is not heartburn. I have difficulty swallowing at times including liquids. Approx 1/7 I had a virtual urgent care visit and was prescribed prednisone 20mg BID x 5 days with non improvement and no worsening. 1/12 I had an in person visit, UA with culture, and was prescribed macrobid for UTI and another 7 days of prednisone. I finished the antibiotics but the prednisone made me very nauseous. I did not complete the course of prednisone. 12/9 I returned for another in person visit. Itchiness has improved however I am still experiencing redness and dermatographia. Started OTC fexofenadine and referral made to dermatologist. At the time of this report 1/8/22, nearly 10 weeks after onset, the esophageal tightness (?stuck food?) and difficulty swallowing persists as well as the dermatographia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- 11/12- UA with culture (positive for UTI) 12/9- ANA, TSH panel, CBC with diff, CMP? all results normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 24.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Gait disturbance
Joint swelling
Symptomtext
All the joints in my body swelled. I had issues walking because it hurt my joints to much. It lasted about 7 days and then started to reduce.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Obesity, anxiety, hypothyroidism, high blood pressure
- Andere Medikamente
- Trileptal - Oxcarbazepine - 600 mg night -anxiety Lexapro - Escitalopram - 20mg night - anxiety Seroquel - Quetiapine - 12.5 mg night - anxiety Lisinopril - 10 mg night - blood pressure Vitamin D3 - 2000 iu night Vitamin C - 500 mg - nig
- Allergien
- Meds I have had issues with: Prednisone- started my period early Alleve - face got itchy Amoxicillin- nipple started to leak Phmb antibiotic - joint pain over whole body Cephalexin - Keflex - Cephalosporins - Joint pain and headache - Arthralgia Meloxicam - rare symptom - puffy eye lids, face Lyrica - made vision do weird things Inactive Ingredient Microcrystalline Cellulose - derived from wood pulp - puffy eye lids and face Inactive Ingredient Cellulose - derived from animal or plant - puffy eye lids and face Medical Grade Honey
- Vorherige Impfungen
- The first two doses of Moderna, age 48, 03/11/2021, 04/06/201. First dose, all over body rash, Second dose, 4" rash and knot a
- Staat
- NJ
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 26.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dysphagia
Urticaria
Symptomtext
Severe uticarial reaction that developed over the course of 3 or 4 days that began to cause difficulty swallowing. I was driven to the ER where I was treated with IV steroids and Benadryl. I was prescribed a 6 day oral steroid treatment and pepcid to take mornings and nights
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 17.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Burning sensation
Rash
Symptomtext
Moderna Covid booster was given 0.25 mL IM at 1350. Symptoms started at 1355. EE stated she started feeling a "burning sensation internally" and said there was a "lace rash on arms and middle of chest.." EE states she started feeling "very anxious" and kept saying "something isn't right." VS taken were 118/71 and HR 64 BPM. Gave Benadryl 12.5 mg oral suspension and monitored EE for another thirty minutes. EE elected to go to the ED. Escorted to ED by RN. VS upon leaving EHS were: BP 137/87 and HR 73 BPM.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Lexapro, Pepcid
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 03.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Loss of personal independence in daily activities
Pain
Pain in extremity
Symptomtext
(11/5/2021-ongoing) Sudden onset sharp pain in upper right arm with movement, rotation, daily activities, etc. Unable to keep arm elevated for more than a few seconds as the pain does not go away. When movement/activity is discontinued, residual pain is still present. Pain has disrupted daily life, unable to perform some activities due to fear of pain. No new or strenuous activities were started before or after onset, and no injuries. Pain scale ranges between 7-9 out of 10. PCP was contacted 11/15/2021, I was told to monitor pain and take ibuprofen As needed and make appointment after one month if pain persists. PCP was seen on 12/7/2021. Ibuprofen 600mg 3/day with meals for 5 days and flexeril 10mg at night. This did not help with pain and pain is still ongoing with no improvements.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- -
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 15.12.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Influenza like illness
Injection site pain
Symptomtext
Severe pain at injection site severe flu like symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zyrtec Ibuprofen
- Allergien
- No known
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 12.12.2021
- Impfdatum
- 30.10.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 30,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Rash
Symptomtext
Shingles - Right T1 dermatome Pain began 11/29/21. Rash erupted 12/3/21. I also have a 39 yo healthy colleague who received both his Influenza Vaccine and Moderna Booster within days of me, and also developed shingles on almost the exact same day I did.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Organ-confined Gleason 7 Prostate Cancer s/p Robotic Prostatectomy 2/19/2021 with negative lymph nodes and PSA undetectable since surgery
- Andere Medikamente
- Lexapro 5 mg PO QD
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Injection site warmth
Nausea
Retching
Symptomtext
Approx. 2 minutes after receiving the Moderna Booster (0.25ml) in left arm, she complained of nausea. Given emesis bag and bottle of water. Denied shortness of breath, denied feeling the her throat was closing, no itching, no hives. I examined injection site, warm to touch, no swelling or redness. She states she hasn't eaten today--given small bag of peanuts. She was still feeling nauseous 8 minutes later. Still sitting in office being observed by nurse. Inquired if she wanted to be checked out in emergency room--she refused. After being observed for another 10 minutes she stated she was feeling less nauseous but says she now has a headache from dry heaving. She decided to return back to her worksite--denied feeling lightheaded or dizzy. Advised to go to Emergency Room if she continues to feel bad.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown.
- Vorgeschichte
- unknown.
- Andere Medikamente
- unknown.
- Allergien
- unknown.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Lymphadenopathy
Neck pain
Pain
Symptomtext
swollen lymph nodes, neck ache, sweating, body ache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 01.12.2021
- Impfdatum
- 27.10.2021
- Beginn
- 14.11.2021
- Tage bis Beginn
- 18,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Hives, started in hands and feet and has become full body. Comes and goes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 29.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Nausea
Pain
Symptomtext
Fatigue, nausea, and pain began 11/30/2021; Took arthritis strength Tylenol and Toradol
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- RSV with pneumonia
- Vorgeschichte
- arthritis, fibromyalgia, asthma, hypertension
- Andere Medikamente
- Wellbutrin 200 mg, Topamax 50mg, losartan 25mg, Singulair 10 mg, estradiol 0.5 mg, Nexium 40mg, Tylenol extra strength sinus and congestion.
- Allergien
- tegretol, codine, hydrocodone, oxycodone, tramadol, sulfa drugs, augmentin, ventyl, penicillin, flonaze, pequin, levaquin, seroquel, ancef, benadryl.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 13.03.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 252,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Inappropriate schedule of product administration
Lethargy
Nausea
Pain
Symptomtext
10 out of 10 pain/pain in every part of body from head to toe; lethargy; severe nausea; headache; inappropriate schedule of vaccine administered; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (10 out of 10 pain/pain in every part of body from head to toe), LETHARGY (lethargy), NAUSEA (severe nausea), HEADACHE (headache) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (inappropriate schedule of vaccine administered) in a 31-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for an unknown indication. No Medical History information was reported. On 13-Mar-2021, the patient received first dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On 03-Apr-2021, received second dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) dosage was changed to 1 dosage form. On 20-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Nov-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (inappropriate schedule of vaccine administered). On an unknown date, the patient experienced PAIN (10 out of 10 pain/pain in every part of body from head to toe), LETHARGY (lethargy), NAUSEA (severe nausea) and HEADACHE (headache). The patient was treated with ACETAMINOPHEN for Adverse event, at a dose of 650 milligram. On 20-Nov-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (inappropriate schedule of vaccine administered) had resolved. At the time of the report, PAIN (10 out of 10 pain/pain in every part of body from head to toe), LETHARGY (lethargy), NAUSEA (severe nausea) and HEADACHE (headache) outcome was unknown. No concomitants medications was reported. This case was linked to MOD-2021-395725 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 27.11.2021
- Impfdatum
- 30.10.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Injection site swelling
Rash
Symptomtext
Client received Flucelvax PF on 10/23/21 at The Clinic and developed a mild injection site reaction (swelling of deltoid) lasting for less than two days; resolved completely. Client received Moderna booster dose 0.25 ml on 10/30/21 with no immediate reports of side effects to his parents. 11 days after receiving his booster, on 11/11/21, he broke out in a rash throughout his body.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- He was seen at The walk-in clinic on 11/14/21 and was prescribed a 8-day tapered course of oral prednisone. He had also been treated with oral antihistamines. At this time, there is no noticeable improvement in his generalized rash - which "comes and goes" - and he will be seen by allergist on 11/29/21. (When seen at the walk-in clinic, it was uncertain whether or not the rash was related to his prior vaccinations. He was told that he might have a skin infection and to wash with Selsun Blue as a precaution, with future consideration for antibiotics.)
- Aktuelle Erkrankungen
- Parents tested positive for breakthrough Covid-19 at the end of September 2021 after receiving both doses of Pfizer greater than two weeks prior; client himself tested negative and never developed any symptoms of infection (fully vaccinated with two doses of Moderna greater than two weeks prior)
- Vorgeschichte
- Anxiety disorder, serious congenital defects, resides at home with parental supervision and care
- Andere Medikamente
- Escitalopram, krill oil, vitamin D - krill oil had been inadvertently doubled by his mother in the interim
- Allergien
- Topiramate (panic attack), dog / cat allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 27.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Dizziness
Feeling abnormal
Headache
Musculoskeletal stiffness
Oedema peripheral
Spinal pain
Symptomtext
10 am brain fog first. Notable dizziness. Then stiffness in neck. Headache started. Then pain in joints and along spine. Chills sometimes severe. No fever. Was hesitant to take Advil but did at 6pm. Then kept up. Symptoms started to ease overnight. Lingering symptoms next day but not severe. Sore arm severe day following vaccine and lasted 3 days. Under arm swelling (arm pit) is bad and still present on Saturday 11/27. No improvement in that. Maybe getting worse. That is the only side effect remaining at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic migraine ,
- Andere Medikamente
- Valtrex, WERA (birth control), Emgality (last injection 11/20/2021, levocetirizine
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 21.11.2021
- Impfdatum
- 17.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Blood test normal
Fatigue
Feeling cold
Nausea
Photophobia
Symptomtext
The next day I was fatigued, cold, and nauseous. I had joint pains and extreme sensitivity to light. Since the vaccine I have still been fatigued every single day. I called my doctor, and she gave me Zofran for the nausea and advised me to rest and drink fluids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Blood work was normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Cushing's disease Addison's disease Diabetes High Blood Pressure
- Andere Medikamente
- Hydrocortisone pills 25mg daily Fludrocortisone 0.1 mg daily Levothyroxine 112mcg daily Nexium 40 mg daily Singulair 10mg daily Crestor 20mg daily Genotropin 0.5mg daily Humalog insulin 3 units with each meal Cymbalta 60mg daily Combi p
- Allergien
- Codeine Penicillin Iodine Sulfa drugs Horses Tetracycline Corn Peanut Butter
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Injection site warmth
Symptomtext
Patient states her right deltoid is red, painful, swollen, and hot posterior to injection site several hours after receiving second dose Moderna covid vaccine. Patient states the area is size of large egg. Patient marked area w/ marker to monitor if area worsens. Patient took Benadryl / Tylenol as needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- zyrtec 10 mg daily, tranex PRN,
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Eosinophil percentage increased
Fatigue
Feeling abnormal
Headache
Injection site erythema
Injection site inflammation
Injection site pain
Laboratory test abnormal
Malaise
Pain
Pyrexia
Ultrasound Doppler normal
Vaccination complication
Symptomtext
approx 12 hrs after receiving the booster I developed what I expected to be normal side effects, fever/chills/ injection site soreness/Headache; approx 16 hrs post booster I developed head to toe body aches, and the headed continued to increase in intensity; I finally took Tylenol approx 20 hrs after receiving the booster, it did alleviate the excruciating headache and body aches, but not the fever; malaise set in approx 24 hrs after receiving the booster and still continues to today. By the 4th day- I still had a fever ranging from 99-102.7 despite 9,000mg of Ibuprofen and Tylenol. My injection site was very sore/inflamed and red. Telemedicine consult told me to report to the E.D. for labs. There they were concerned about my arm. They checked for cellulitis and an abscess. They determined it to be an reaction to the booster. My fever was 99.0 at the E.D. They told me to cont with NSAIDs and to use warm compresses on my arm. I followed up with my PCP 8 days post booster. Labs were completed and I was shown to have elevated Eosinophils (8.3%) I am now 12 days post booster and I still feel very fatigued and a little bit of 'brain fog'
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- 11/6/2021ultrasound of right arm- no cellulitis no abscess 11/11/2021 CBB labs elevated eosinophils 8.3%
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- polycystic ovarian syndrome tachycardia
- Andere Medikamente
- Metformin ( for polycystic ovarian syndrome) metropolol
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 14.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Balance disorder
Computerised tomogram head
Computerised tomogram neck
Laboratory test
Magnetic resonance imaging
Nausea
Nystagmus
Vertigo
Vestibular neuronitis
Vomiting
Symptomtext
Sudden onset extreme vertigo, nausea, vomiting, balance difficulties, nystagmus. Taken to hospital for Sroke Protocol. Stroke ruled out by CT and MRI. 3 days in hospital diagnosed with vestibular neuritis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- 3,0
- Labordaten
- Many lab tests, MRI, CT of head and neck, neuro assessments, telemetry, physical therapy. Ruled out ?crystals?. (Benign paroxysmal something something)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Celiac disease
- Andere Medikamente
- Estradiol, Flonase, D3, B12, doxycycline, omeprazole, baclofen, Benadryl, Allerclear
- Allergien
- Gluten
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 13.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Fatigue
Headache
Hypersomnia
Influenza like illness
Muscle spasms
Nausea
Somnolence
Symptomtext
Joint muscle cramps in his legs; like a mild case of the flu; pretty much slept; Tired; Sleepy; Joint pain; Low grade nausea; Headache; This spontaneous case was reported by a consumer and describes the occurrence of SOMNOLENCE (Sleepy), MUSCLE SPASMS (Joint muscle cramps in his legs), INFLUENZA LIKE ILLNESS (like a mild case of the flu), HYPERSOMNIA (pretty much slept) and ARTHRALGIA (Joint pain) in a 72-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 02-Nov-2021, the patient experienced SOMNOLENCE (Sleepy), ARTHRALGIA (Joint pain), NAUSEA (Low grade nausea) and HEADACHE (Headache). On 03-Nov-2021, the patient experienced HYPERSOMNIA (pretty much slept) and FATIGUE (Tired). On an unknown date, the patient experienced MUSCLE SPASMS (Joint muscle cramps in his legs) and INFLUENZA LIKE ILLNESS (like a mild case of the flu). At the time of the report, SOMNOLENCE (Sleepy), MUSCLE SPASMS (Joint muscle cramps in his legs), INFLUENZA LIKE ILLNESS (like a mild case of the flu), HYPERSOMNIA (pretty much slept), ARTHRALGIA (Joint pain), NAUSEA (Low grade nausea), HEADACHE (Headache) and FATIGUE (Tired) had resolved. No Concomitant product use was reported. No treatment information was provided. The patient just got the booster of the Moderna vaccine and on that same day the patient had headache, joint pain, was sleepy and had low grade nausea but nothing serious. The next day they pretty much slept, and was tired, but now nothing. Reportedly, the patient also had joint muscle cramps in their legs. The patient was also confused if these effects came from the shot or not it would be like a mild case of the flu. This case concerns a 72-year-old male patient with no relevant medical history who experienced non-serious unexpected events of Somnolence, Muscle spasms, Hypersomnia, Influenza like illness, and non-serious expected events of Arthralgia, Nausea, Headache and Fatigue. The events occurred on the same day or the day after the third dose of Moderna COVID-19 vaccine. Temporal relationship for the events Muscle spasms and Influenza like illness is unknown as start date of the events was not provided. The rechallenge was not applicable as the events occurred following the third dose. Very limited information regarding clinical course of the events has been provided at this time. The benefit-risk relationship of Moderna COVID-19 vaccine is not affected by this report.; Sender's Comments: This case concerns a 72-year-old male patient with no relevant medical history who experienced non-serious unexpected events of Somnolence, Muscle spasms, Hypersomnia, Influenza like illness, and non-serious expected events of Arthralgia, Nausea, Headache and Fatigue. The events occurred on the same day or the day after the third dose of Moderna COVID-19 vaccine. Temporal relationship for the events Muscle spasms and Influenza like illness is unknown as start date of the events was not provided. The rechallenge was not applicable as the events occurred following the third dose. Very limited information regarding clinical course of the events has been provided at this time. The benefit-risk relationship of Moderna COVID-19 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain
Pain in extremity
Skin warm
Tenderness
Symptomtext
15cm reddened area to arm, red and warm to touch, pain in arm when moving or touching
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Morbid Obesity, Major Depressive disorder, Chronic pain, GERD, OSA, chronic kidney disease stage 3, Hypothyroidism, Chronic respiratory failure with hypoxia, chronic respiratory failure with hypercapnia
- Andere Medikamente
- Belbuca film, Bupropion HCI ER, Trazadone, Famotidine, Furosemide, Gabapentin, Levothyroxine Sodium, Melatonin, Methocarbamol, Oxycodone, Sertraline
- Allergien
- Clindamycin, Codeine, Ferrous Sulfate, Ibuprofen, Imipenem, Sulfamethoxazole/Trimethoprim, Cephalosporins, Penicillins, Sulfa Antibiotics, Honey, Walnuts, Neomycin, adhesive tape, silicones, ag mesh, cilastatin, honey bee venom, latex, nystatin, orange extract, Tegaderm, trimethoprim
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Fatigue
Hyperhidrosis
Muscle spasms
Myalgia
Nausea
Pain
Pyrexia
Symptomtext
11/03/2021 - 10am - received shot; 8pm - fatigued & chills; 10pm - severe chills & severe muscle aches/cramping; 12am - nausea, continued chills & muscle aches. 11/04/2021 - 6am - fever 103.1, chills, nausea, body aches; 10am -fever broke and body/clothes drenched in sweat; 11am -4pm - fatigued and chills; 7pm - fever returns at 101.1 with chills and body aches; 9pm - nausea with chills throughout the night. 11/05-2021 - 7am - fatigued, slight muscle aches, no energy continued all day through 11/06/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Buproprion, Escitalopram, Claritin
- Allergien
- None
- Vorherige Impfungen
- 03/03/2021 - Covid (Moderna) with same symptoms
- Staat
- OH
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 08.11.2021
- Impfdatum
- 07.07.2021
- Beginn
- 08.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pain in extremity
Symptomtext
Per patient had local pain at injection site after first dose. Was told that it should resolve in a couple of days. Was still advised to complete the series with a second dose a month later. Since then patient says has been having throbbing pain in the injection arm( left arm) of about 2-3 on a scale of 10 and at times pain is up to 5 on 10. Considering when patient had his second dose of moderna, i counseled the patient to seek medical attention further consultation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Nabumetone
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature increased
Chills
Fatigue
Pain
Pain in extremity
Symptomtext
18 hours after vaccination woken up with chills . Temp 100.8, severe body aches, sore arm, fatigue. Treatment : ibuprofen, ice , fluids, sleep. 60% improved 48 hours after vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroid, restless legs, migraine, anxiety
- Andere Medikamente
- Levothyroxine, pramioaxole, citalipram
- Allergien
- Fire ant anaphylaxis
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 07.10.2021
- Beginn
- 07.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Rash
Symptomtext
Patient states that she experience rash on her upper right arm and underarm on following vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Rash across abdomen
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none
- Andere Medikamente
- Magnesium supplement (Calm)
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 31.10.2021
- Impfdatum
- 31.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthropod bite
Erythema
Pruritus
Rash
Symptomtext
Patient vaccinated approximately 2:10 and left observation area after 15 minutes. She returned to observation @2:35pm complaining of rash, redness, and itching on right inner arm, opposite arm of injection site. Patient states bitten by mosquito earlier and noticed some itching on right arm, after leaving observation she developed a rash, redness, and itching on right arm. Obtained vitals signs and administered 25mg of benadryl by mouth. Continuedto observe until 3:05pm, symptoms decreased significantly. No acute distess noted. Advised to seek medical attention for worsening/returning symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- 10/31/21 BP 140/82, Pulse 84, RR 16, Pulse Ox 98%
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Injection site reaction
Symptomtext
Patient was given .5ml of moderna instead of .25ml Patient complained of local reaction at the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- atrial fibrillation arthralgia of the lower leg dilated cardiomyopathy HTN
- Andere Medikamente
- Unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Incorrect dose administered
Malaise
Pyrexia
Symptomtext
Patient was given .5ml of moderna instead of the .25ml Patient complained of fever, chills, malaise.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- None- patient did not indicate. Works @ a school
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- F
- Eingang
- 21.10.2021
- Impfdatum
- 03.09.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Computerised tomogram head normal
Headache
Impaired work ability
Symptomtext
Headaches/Frontal started 9/4/21 day after vaccine # 1, After vaccine #2 headaches now severe, Intolerable, had to call in sick for work today, 10-7-21. Had to take Florcet for pain-No prior migraines
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Cat Scan Head-Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic tachycardia, depression,
- Andere Medikamente
- Zoloft, Metoprolol,
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 20.10.2021
- Impfdatum
- 21.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Rash pruritic
Symptomtext
arm soreness, itchy w/bumps
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- sulfamethoxazole-trimethoprim macrodantin bactrim DS Benadryl
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 18.10.2021
- Impfdatum
- 18.07.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 75,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Loss of personal independence in daily activities
Muscle twitching
Symptomtext
Over the past several weeks, I have had uncontrollable 'twitching' in my left hand. Primarily between thumb and index finger. Thought it may be a side effect of perscribed med I took for a short time. but I have stopped all perscriptions as none of them were working to help headaches. Twitiching has not continued, but has become somewhat bothersome. I have dropped a cup and have a lot of trouble carring bags and such.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- NA. I have a 5K deductable and have already spent several hundred dollars and nothing has brought relief so far.
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- oxybutin, allipuronol, lisonopril, multi vit, herbal headache, 2 other herbal supplement (cant recall names)
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 14.10.2021
- Impfdatum
- 28.09.2021
- Beginn
- 08.10.2021
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysphagia
Lymphadenopathy
Oropharyngeal pain
Stomatitis
Symptomtext
11 days after the shot big sores grew on my palate. Throat is sore glands are inflamed and its hard to eat because of the sores. After six days with no change I called the clinic and have an appt next week. never had this in my life
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- will do next week
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- migraines
- Andere Medikamente
- bupropion, zolmetriptan
- Allergien
- ciproflaxin, rag weed, blue dye
- Vorherige Impfungen
- flu vax
- Staat
- TN
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 12.10.2021
- Impfdatum
- 08.10.2021
- Beginn
- 08.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Symptomtext
LARGE WARM RED RASH ON LEFT ARM
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE
- Andere Medikamente
- UNKNOWN
- Allergien
- NO KNOWN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 11.10.2021
- Impfdatum
- 13.09.2021
- Beginn
- 07.10.2021
- Tage bis Beginn
- 24,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Abdominal pain
Cough
Diarrhoea
Headache
Nausea
Pyrexia
Rhinorrhoea
Vomiting
Symptomtext
fever, runny nose, headache, cough, nausea, vomiting, diarrhea, abdominal pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 10.10.2021
- Impfdatum
- 30.09.2021
- Beginn
- 07.10.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Discomfort
Erythema
Induration
Peripheral swelling
Pruritus
Skin warm
Symptomtext
On the evening of October 7, 2020, I developed a firm bump in my left arm where I received the vaccine. It was itchy and uncomfortable. The next morning I woke up with a 3inch red circle that was slightly raised, firm, warm to the touch, and itchy. October 10, the circle is no longer raised or warm to the touch but still visible, itchy, and uncomfortable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Prenatal Vitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 09.10.2021
- Impfdatum
- 11.09.2021
- Beginn
- 12.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pain in extremity
Symptomtext
Patient reports soreness in his vaccinated arm, which started the next day and lingered for two weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 08.10.2021
- Impfdatum
- 07.10.2021
- Beginn
- 07.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Nasal oedema
Urticaria
Symptomtext
Patient reports hives, facial, lip and nose edema, and chest pressure. Took allergy med and Tylenol and all resolved today except for some nose edema. Of note she has had dermal fillers in her face and nose 6 years ago,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- dermal fillers 6 years ago
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 06.10.2021
- Impfdatum
- 05.10.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Decreased appetite
Diarrhoea
Fatigue
Headache
Nausea
Neck pain
Pain in extremity
Symptomtext
continual mild headache, fatigue, nausea, soreness in arm/shoulder/neck, loss of appetite, diarrhea; all lasting first 24 hours after shot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 04.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Product administered to patient of inappropriate age
Somnolence
Symptomtext
Patient was inadvertently administered the vaccine. The patient is currently too young to receive the Moderna Covid-19 vaccine under the current Emergency Use Authorization. Patient has not experienced any symptoms out of the ordinary. He has a headache and slept most of the next day following vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 29.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Chills
Dizziness
Feeding disorder
Feeling cold
Headache
Illness
Lymphadenopathy
Myalgia
Pyrexia
Symptomtext
I received the first shot March 6, 2021. I was sick the whole next day. I received my second shot on April 3, 2021. I was sick for 3 days after that one. I had swollen glands that lasted for 2-3 weeks. I got my third shot on September 29, 2021 and I was sick for just over 3 days. I had severe muscle aches starting in early morning after the shot that lasted about 2 days. I had swollen glands on the collarbone on the injection side. I had chills , fevers and weakness for almost 4 days during that time I slept in my winter coat under my bedcovers. When I got out of bed I felt dizzy. I couldn?t eat for the first 3 days. I had severe headaches for the first 2 days after the shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Rheumatoid arthritis
- Andere Medikamente
- Methotrexate, Celebrex, folic acid, hydrochlorothiazide, atorvastatin, multi-vitamin, vitamin D, Calcium
- Allergien
- -
- Vorherige Impfungen
- Shingles, flu vaccine and every covid vaccine
- Staat
- PA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 02.10.2021
- Impfdatum
- 20.01.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 246,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Lymphadenopathy
Pyrexia
Vaccination site pain
Vaccination site swelling
Symptomtext
Fever; Joint pain in arms and legs; arm is very sore and swollen on the top (injection site); arm is very sore and swollen on the top (injection site); Supraclavicular swelling, a lymph node is swollen; This spontaneous case was reported by an other health care professional and describes the occurrence of PYREXIA (Fever), ARTHRALGIA (Joint pain in arms and legs), VACCINATION SITE PAIN (arm is very sore and swollen on the top (injection site)), VACCINATION SITE SWELLING (arm is very sore and swollen on the top (injection site)) and LYMPHADENOPATHY (Supraclavicular swelling, a lymph node is swollen) in a 46-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 013M20A and 012L20A) for COVID-19 vaccination. The patient's past medical history included Viral infection NOS in March 2020. Concurrent medical conditions included Viral myocarditis (Cardiomyopathy) in June 2020 and Sleep disorder. Concomitant products included HYDROXYCHLOROQUINE, VITAMIN D NOS, FAMOTIDINE, VITAMIN B12 NOS (VITAMIN B 12 [VITAMIN B12 NOS]), FISH OIL and LEVOTHYROXINE SODIUM (SYNTHROID) for an unknown indication. On 20-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 17-Feb-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 22-Sep-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 23-Sep-2021, the patient experienced PYREXIA (Fever), ARTHRALGIA (Joint pain in arms and legs), VACCINATION SITE PAIN (arm is very sore and swollen on the top (injection site)), VACCINATION SITE SWELLING (arm is very sore and swollen on the top (injection site)) and LYMPHADENOPATHY (Supraclavicular swelling, a lymph node is swollen). The patient was treated with HYDROXYCHLOROQUINE SULFATE (PLAQUENIL [HYDROXYCHLOROQUINE SULFATE]) for Tendinitis, at an unspecified dose and frequency and SULFASALAZINE ongoing from March 2021 for Tendinitis, at an unspecified dose and frequency. At the time of the report, PYREXIA (Fever), ARTHRALGIA (Joint pain in arms and legs), VACCINATION SITE PAIN (arm is very sore and swollen on the top (injection site)), VACCINATION SITE SWELLING (arm is very sore and swollen on the top (injection site)) and LYMPHADENOPATHY (Supraclavicular swelling, a lymph node is swollen) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patients concomitant medications include Medication for sleep disorder. Lot number for 3rd dose of the vaccine reported as 0 (4 or 7) (5 or S) C21A. The patient used ice. This case was linked to MOD-2021-331260, MOD-2021-331212 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Sleep disorder
- Vorgeschichte
- Medical History/Concurrent Conditions: Viral infection NOS; Viral myocarditis (Cardiomyopathy).
- Andere Medikamente
- Hydroxychloroquine; Vitamin D Nos; Famotidine; Vitamin B 12 [Vitamin B12 Nos]; Fish Oil; Synthroid
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 01.10.2021
- Impfdatum
- 16.09.2021
- Beginn
- 16.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Contusion
Diarrhoea
Headache
Illness
Pyrexia
Vaccination site reaction
Symptomtext
Magnet stuck to her arm on injection site; still has a bruise on her arm; Just plumb sick/sick as a dog; Diarrhea for 2 days; Two hours after the shot, she was on the couch with chills; Two hours after the shot, she was on the couch with fever; Two hours after the shot, she was on the couch with headache; This spontaneous case was reported by a consumer and describes the occurrence of CONTUSION (still has a bruise on her arm), ILLNESS (Just plumb sick/sick as a dog), VACCINATION SITE REACTION (Magnet stuck to her arm on injection site), DIARRHOEA (Diarrhea for 2 days) and CHILLS (Two hours after the shot, she was on the couch with chills) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 16-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Sep-2021, the patient experienced ILLNESS (Just plumb sick/sick as a dog), DIARRHOEA (Diarrhea for 2 days), CHILLS (Two hours after the shot, she was on the couch with chills), PYREXIA (Two hours after the shot, she was on the couch with fever) and HEADACHE (Two hours after the shot, she was on the couch with headache). On 21-Sep-2021, the patient experienced CONTUSION (still has a bruise on her arm). On an unknown date, the patient experienced VACCINATION SITE REACTION (Magnet stuck to her arm on injection site). On 18-Sep-2021, DIARRHOEA (Diarrhea for 2 days) had resolved. At the time of the report, CONTUSION (still has a bruise on her arm) had not resolved and ILLNESS (Just plumb sick/sick as a dog), VACCINATION SITE REACTION (Magnet stuck to her arm on injection site), CHILLS (Two hours after the shot, she was on the couch with chills), PYREXIA (Two hours after the shot, she was on the couch with fever) and HEADACHE (Two hours after the shot, she was on the couch with headache) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medication was not provided. the patient saw a doctor who put her on antibiotics and ruled out Covid and the flu Most recent FOLLOW-UP information incorporated above includes: On 28-Sep-2021: Follow-up include no new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- -
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- 20.09.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Myalgia
Pyrexia
Symptomtext
started experiencing a headache while waiting in the observation room for 15 minutes; fever; chills; body ache; fatigue; This spontaneous case was reported by a consumer and describes the occurrence of HEADACHE (started experiencing a headache while waiting in the observation room for 15 minutes), PYREXIA (fever), CHILLS (chills), MYALGIA (body ache) and FATIGUE (fatigue) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. Concurrent medical conditions included Blood pressure abnormal and Asthma. Concomitant products included BUDESONIDE, FORMOTEROL FUMARATE (SYMBICORT) for Asthma, HYDROCHLOROTHIAZIDE for Blood pressure. On 20-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Sep-2021, the patient experienced HEADACHE (started experiencing a headache while waiting in the observation room for 15 minutes), PYREXIA (fever), CHILLS (chills), MYALGIA (body ache) and FATIGUE (fatigue). The patient was treated with PARACETAMOL (TYLENOL) for Fever, at an unspecified dose and frequency. At the time of the report, HEADACHE (started experiencing a headache while waiting in the observation room for 15 minutes), PYREXIA (fever), CHILLS (chills), MYALGIA (body ache) and FATIGUE (fatigue) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. The patient reported that the fever comes back as soon as the effect of the Tylenol wears off.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Asthma; Blood pressure abnormal
- Vorgeschichte
- -
- Andere Medikamente
- HYDROCHLOROTHIAZIDE; SYMBICORT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 29.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 25.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Anosmia
Fatigue
Feeling abnormal
Headache
Impaired work ability
Pain
SARS-CoV-2 test negative
Symptomtext
Took shot on Friday, 9/24/2021. Woke up 9/25/2021 unable to smell or taste and with headache, body ache and fatigue. Progressively got worse. Unable to go to work. Took home test for Covid on 9/28/2021 and was negative. Talked to nurse through my insurance company who said if I still had symptoms the next day to follow up with a doctor. I did that today, 9/29/2021. Tested negative at dr office with rapid test. Still feel like crap, no smell or taste and headache, extreme fatigue, body aches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 9/28/2021 at home Covid test negative 9/29/2021 rapid test at dr office negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Pacemaker for sick sinus syndrome Hypertension
- Andere Medikamente
- Levothyroxine, Estradiol, Trintellex, magnesium, Iron, multi vitamin, cranberry
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 29.09.2021
- Impfdatum
- 28.09.2021
- Beginn
- 29.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose increased
Blood pressure increased
Pain in extremity
Stress
Swollen tongue
Symptomtext
tongue swelling, arm pain, elevated blood sugar, elevated blood pressure, stress about vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Nervous; Carpal tunnel syndrome Cerebrovascular accident (CVA) due to thrombosis of cerebral artery Chronic pain of right knee Left shoulder pain Stroke (From Hx)Circulatory; Diabetes mellitus with coincident hypertension; Hypertension; Hypertension, uncontrolled Digestive; Class 3 severe obesity in adult; Fatty liver; Endocrine/Metabolism; High cholesterol; Hyperlipidemia (Resolved); 12/21/2017; Pure hypercholesterolemia (Resolved); 06/29/2020; Type 2 diabetes mellitus with hyperlipidemia Immune Allergic Drug-induced lupus erythematosus (Resolved) 01/17/2019 Other Abnormal LFTs Abnormal serum protein test
- Andere Medikamente
- amLODIPine (NORVASC) 10 mg tablet atorvastatin (LIPITOR) 10 mg tablet baclofen (GABLOFEN) 10 mg tablet butalbital-acetaminophen-caffeine (FIORICET) 50-325-40 mg per tablet clopidogreL (PLAVIX) 75 mg tablet ERGOCALCIFEROL, VITAMIN D2, (
- Allergien
- Penicillin G Rash Aspirin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 24.09.2021
- Impfdatum
- 07.09.2021
- Beginn
- 11.09.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Injection site pain
Injection site pruritus
Injection site rash
Injection site swelling
Rash
Symptomtext
approx. 4 days following this 3rd dose of the Moderna vaccine, an itchy rash appeared at the injection site (upper right arm) which had been painful/swollen for 3-4 days. Shortly thereafter, the rash appeared on my upper right thigh (inner and outer) as well as right buttock. It also appeared to a lesser extent on my right ankle, as well as on my lower back. The rash also occurred on my outer and inner left thigh. Saw the dermatologist today and he suggested either a shot of Kenalog (which i declined) or topical cream to apply 2X/day. I don't know the cream name, but will pick it up tomorrow. Note: i've had no changes to diet, supplements, or lotions. . On 08/26/21, recvd cortisone shot in left shoulder joint
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- no acute illnesses (rotator-cuff tendinitis for months)
- Vorgeschichte
- cough-variant asthma, depression, GERD, osteoporosis, and RA
- Andere Medikamente
- citalopram; Asmanex; omeprazole; Prolia; methotrexate
- Allergien
- sulfa, zithromax
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 21.09.2021
- Impfdatum
- 16.09.2021
- Beginn
- 16.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood culture
Culture urine
Fatigue
Headache
Influenza A virus test negative
Influenza virus test negative
Pain
Pyrexia
SARS-CoV-2 test negative
Symptomtext
Received vaccine on Thursday and by evening, fatigue, achy, headaches and fever. Friday was worsening of those symptoms. Continued through Monday when I went to Emergency room with temp 103.9 and headaches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Emergency room visit Monday 9/20/21 Covid test negative Flu A and B negative Blood Cultures pending Urine Culture pending
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Vitamin D3 B12 Iron 325mg Dandelion Capsule 450mg Multi Vitamin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 18.09.2021
- Impfdatum
- 17.09.2021
- Beginn
- 17.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site rash
Injection site swelling
Injection site warmth
Vaccine positive rechallenge
Symptomtext
Patient had swelling "like an egg" , rash, and fever in arm at site starting the night she received vaccination. Patient said she had same with the first dose (opposite arm) that lasted at least a week. Pharmacist recommended tylenol and benadryl for "COVID arm" symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- same reaction with previous dose of covid
- Staat
- GA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 09.09.2021
- Beginn
- 10.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Fatigue
Injection site warmth
Myalgia
Pruritus
Symptomtext
Pt. states that after receiving the 3rd Booster dose of Moderna 09/09/2021, started experiencing symptoms 09/10/2021 of fatigue, muscle pain, and itchiness. Injection site hot to the touch. No noted Primary visit. Still experiencing symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HBP
- Andere Medikamente
- Tramadol, Trazodone, Esterdiol, Lisinopril, Benadryl, Nasacort
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 14.09.2021
- Impfdatum
- 09.09.2021
- Beginn
- 10.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Pain in extremity
Sleep disorder
Symptomtext
Severe pain in arm and shoulder starting the day after vaccination. This occurred after the "booster" dose was administered. Hot pads, OTC lidocaine, ice packs, massage therapy, and OTC Tylenol have been given to relieve the pain but nothing seems to work. Wakes patient up at night due to severity of pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 13.09.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Lip swelling
Pain in extremity
Symptomtext
During screening process for second dose, was reviewing any reactions to first dose and pt stated had sore arm and experienced lip swelling. Did not state how long experienced for nor did she state that she took any OTC medications for treatment. Pt did not experience swealling of mouth or throat or difficulty breathing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- none - pt did not seek medical attnetion
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- none known
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.09.2021
- Impfdatum
- 08.09.2021
- Beginn
- 10.09.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site pruritus
Injection site swelling
Symptomtext
Patient presented to the clinic with complaints of itching, soreness and swelling at the injection site. Symptoms appeared localized and patient was instructed to use benadryl cream and ice packs through resolution of symptoms. Contacted patient 9/13 for follow-up: Soreness has resolved. Itching still remains - placing benadryl three times daily to site. Patient has an appointment with NP on wednesday. If not resolved by then, patient will review with NP
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Not Assessed
- Vorgeschichte
- Not Assessed
- Andere Medikamente
- Vancomycin PO
- Allergien
- PCN, Morphine, Erythromycin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 11.09.2021
- Impfdatum
- 03.09.2021
- Beginn
- 11.09.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash erythematous
Rash pruritic
Symptomtext
Itchy circular red rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash erythematous
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- No
- Andere Medikamente
- Multivitamin, zinc, iron, bcaas, preworkout, vit d, calcium
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 11.09.2021
- Impfdatum
- 30.08.2021
- Beginn
- 30.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cold sweat
Dizziness
Feeling cold
Rash
Symptomtext
almost passed out; body is cold; He's having a cold sweat, body is cold; He has a rash underneath both armpits; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (almost passed out), FEELING COLD (body is cold), COLD SWEAT (He's having a cold sweat, body is cold) and RASH (He has a rash underneath both armpits) in a 70-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 30-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Aug-2021, the patient experienced DIZZINESS (almost passed out), FEELING COLD (body is cold), COLD SWEAT (He's having a cold sweat, body is cold) and RASH (He has a rash underneath both armpits). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at a dose of 1 dosage form. At the time of the report, DIZZINESS (almost passed out) outcome was unknown and FEELING COLD (body is cold), COLD SWEAT (He's having a cold sweat, body is cold) and RASH (He has a rash underneath both armpits) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medication was reported. No treatment medications was reported. Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.; Sender's Comments: Based on the current available information and temporal association between the use of the product and the start date of the events, a causal relationship cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 11.09.2021
- Impfdatum
- 15.08.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Myalgia
Papule
Peripheral swelling
Symptomtext
a little bit pink\ raised\ tiny bumps starting to appear on top of my shoulder; sore arm; swelling; This spontaneous case was reported by a consumer and describes the occurrence of PERIPHERAL SWELLING (swelling), PAPULE (a little bit pink\ raised\ tiny bumps starting to appear on top of my shoulder) and MYALGIA (sore arm) in a 25-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Aug-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Aug-2021, the patient experienced PERIPHERAL SWELLING (swelling) and MYALGIA (sore arm). On 17-Aug-2021, the patient experienced PAPULE (a little bit pink\ raised\ tiny bumps starting to appear on top of my shoulder). At the time of the report, PERIPHERAL SWELLING (swelling), PAPULE (a little bit pink\ raised\ tiny bumps starting to appear on top of my shoulder) and MYALGIA (sore arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No Concomitant and Treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 09.09.2021
- Impfdatum
- 07.09.2021
- Beginn
- 08.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Extra dose administered
Feeling cold
Headache
Hot flush
Influenza like illness
Interchange of vaccine products
Malaise
Pain
Symptomtext
Hot/ cold flashes, headache, body aches, not hungry. I felt like I had the 24hr flu after my second dose of Pfizer, but this booster dose of Moderna has been way worse. Still sick and unsure how long this will last.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Scoliosis
- Andere Medikamente
- Acyclovir
- Allergien
- Sensitive to gluten, dairy, and latex
- Vorherige Impfungen
- I was 30yrs old when I received my second dose of Pfizer COVID-19 vaccine on 1/29/21. I had hot/ cold flashes, body aches, nause
- Staat
- PA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 09.09.2021
- Impfdatum
- 08.09.2021
- Beginn
- 08.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cough
Eye irritation
Fatigue
Headache
Nasal congestion
Pain
Pollakiuria
Pyrexia
Symptomtext
chills, fever, body aches, coughing, stuffy nose, headache, burning eyes, fatigue, frequent urination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- -
- Andere Medikamente
- ANASTROZOLE, RIBOCICLIB
- Allergien
- SULFA, PENICILLIAN, LEVOQUIN
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 08.09.2021
- Impfdatum
- 11.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood cholesterol increased
Blood test normal
Dizziness
Dizziness postural
Dry mouth
Ear pain
Feeling abnormal
Feeling hot
Impaired work ability
Labyrinthitis
Malaise
Nausea
Otitis externa
Polydipsia
Thirst
Symptomtext
The day after the vaccine, 08/12/2021 at 04:30 PM, I was out of town, I was totally fine the whole morning, I had an overwhelming feeling dizziness and nausea. I was hot, and thirsty. I was drinking lot of water. I couldn't get rid of the thirst. I had an extremely dry mouth. I was only feeling well if I was laying down, I couldn't be sitting or standing. A few days after I had extreme pain on my right ear. I was taking ibuprofen and it wasn't helping. I went to the clinic , on 08/16/2021 for my ear. and I ended up having a double infection in my inner and outer ear. With my ear infection I was prescribed Amoxicillin antibiotic, she prescribed 7 days worth , at the 7 day mark it still didn't feel completely right. I called my doctor yesterday to see if it was ok to get the 2nd dose, She said its probably something in my inner ear that's causing the nausea and to go ahead and get the 2nd dose tomorrow, 09/09/2021. This Tues. 08/31/2021 around 1:00 pm I had another spell of dizziness and nausea and had to leave early from work because I felt like I was going to pass out. I still have the dry mouth and excessive thirst. The last time I felt bad was last Thursday ,09/02/2021, At work at school, the motion of the kids walking in different directions made me nausea. Same for Friday, picking up something up from the floor makes me feel dizzy. I still have dizziness a little but I am extremely thirsty, more than usual. I have a telehealth appointment with my doctor on Monday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- blood work done after the ear infection- everything was normal except my cholesterol was a little bit high
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- no
- Andere Medikamente
- Lexapro 30 mg od
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 07.09.2021
- Impfdatum
- 02.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Urticaria
Symptomtext
Urticaria Started Day After Vaccine. Received Medrol Dose Pak, Famotidine And Benadryl from ER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes, HTN, Smoker
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 02.09.2021
- Impfdatum
- 11.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
Headache
Nausea
Pain in extremity
Tenderness
Symptomtext
there was a sewer smell and she couldn't smell it; tender; when she is laying down on her side, it hurts/her left arm is still sore and still aggravates her; nausea; had a headache every day for almost a whole week since vaccination; This spontaneous case was reported by a consumer and describes the occurrence of ANOSMIA (there was a sewer smell and she couldn't smell it), TENDERNESS (tender), PAIN IN EXTREMITY (when she is laying down on her side, it hurts/her left arm is still sore and still aggravates her), NAUSEA (nausea) and HEADACHE (had a headache every day for almost a whole week since vaccination) in a 51-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. The patient's past medical history included Heart failure. Concurrent medical conditions included Diabetes, Blood pressure high and Neuropathy. Concomitant products included METFORMIN, GLIMEPIRIDE, LISINOPRIL, GABAPENTIN (NEURONTIN) and DULOXETINE HYDROCHLORIDE (CYMBALTA) for an unknown indication. On 11-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In August 2021, the patient experienced ANOSMIA (there was a sewer smell and she couldn't smell it). August 2021, the patient experienced TENDERNESS (tender), PAIN IN EXTREMITY (when she is laying down on her side, it hurts/her left arm is still sore and still aggravates her), NAUSEA (nausea) and HEADACHE (had a headache every day for almost a whole week since vaccination). The patient was treated with PARACETAMOL (TYLENOL) for Headache, at a dose of 220 mg. At the time of the report, ANOSMIA (there was a sewer smell and she couldn't smell it), TENDERNESS (tender), PAIN IN EXTREMITY (when she is laying down on her side, it hurts/her left arm is still sore and still aggravates her), NAUSEA (nausea) and HEADACHE (had a headache every day for almost a whole week since vaccination) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Blood pressure high; Diabetes; Neuropathy
- Vorgeschichte
- Medical History/Concurrent Conditions: Heart failure
- Andere Medikamente
- METFORMIN; GLIMEPIRIDE; LISINOPRIL; NEURONTIN; CYMBALTA
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 31.08.2021
- Impfdatum
- 17.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Inflammation
Pain
Pain in extremity
Symptomtext
Left arm hurts more than when they got the second dose; Pain feels muscular and inflamed and has spread across the chest, mostly over the left breast area; The pain feels muscular and inflamed; Headache; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Left arm hurts more than when they got the second dose), PAIN (Pain feels muscular and inflamed and has spread across the chest, mostly over the left breast area), INFLAMMATION (The pain feels muscular and inflamed) and HEADACHE (Headache) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. Concomitant products included HYDROXYCHLOROQUINE SULFATE (PLAQUENIL S), PREGABALIN, PREDNISONE, MYCOPHENOLATE MOFETIL HYDROCHLORIDE (CELLCEPT [MYCOPHENOLATE MOFETIL HYDROCHLORIDE]), CELECOXIB (CELEBREX), VITAMIN B12 NOS, BELIMUMAB, LANSOPRAZOLE, IRON and RIBOFLAVIN for an unknown indication. On 17-Aug-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Aug-2021, the patient experienced HEADACHE (Headache). On an unknown date, the patient experienced PAIN IN EXTREMITY (Left arm hurts more than when they got the second dose), PAIN (Pain feels muscular and inflamed and has spread across the chest, mostly over the left breast area) and INFLAMMATION (The pain feels muscular and inflamed). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency. On 18-Aug-2021, HEADACHE (Headache) had resolved. At the time of the report, PAIN IN EXTREMITY (Left arm hurts more than when they got the second dose), PAIN (Pain feels muscular and inflamed and has spread across the chest, mostly over the left breast area) and INFLAMMATION (The pain feels muscular and inflamed) outcome was unknown. This case was linked to MOD-2021-290856 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No Medical History information was reported.
- Andere Medikamente
- PLAQUENIL S; PREGABALIN; PREDNISONE; CELLCEPT [MYCOPHENOLATE MOFETIL HYDROCHLORIDE]; CELEBREX; VITAMIN B12 NOS; BELIMUMAB; LANSOPRAZOLE; IRON; RIBOFLAVIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 06.07.2021
- Beginn
- 07.08.2021
- Tage bis Beginn
- 32,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Injection site pain
Lymph node pain
Nodule
Peripheral swelling
Symptomtext
2 little balls or nodules very close together on her left clavicle that were painful to touch; Left arm pit was swollen; Next to her chest beside her breast was painful; Under her arm was painful; Left Arm hurt; This spontaneous case was reported by a consumer and describes the occurrence of NODULE (2 little balls or nodules very close together on her left clavicle that were painful to touch), PERIPHERAL SWELLING (Left arm pit was swollen), LYMPH NODE PAIN (Next to her chest beside her breast was painful), INJECTION SITE PAIN (Left Arm hurt) and AXILLARY PAIN (Under her arm was painful) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 045C21A and 045C21A) for COVID-19 vaccination. Concurrent medical conditions included Menopause. On 06-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 07-Aug-2021, the patient experienced INJECTION SITE PAIN (Left Arm hurt). On 09-Aug-2021 at 6:00 PM, the patient experienced NODULE (2 little balls or nodules very close together on her left clavicle that were painful to touch), PERIPHERAL SWELLING (Left arm pit was swollen), LYMPH NODE PAIN (Next to her chest beside her breast was painful) and AXILLARY PAIN (Under her arm was painful). At the time of the report, NODULE (2 little balls or nodules very close together on her left clavicle that were painful to touch) was resolving and PERIPHERAL SWELLING (Left arm pit was swollen), LYMPH NODE PAIN (Next to her chest beside her breast was painful), INJECTION SITE PAIN (Left Arm hurt) and AXILLARY PAIN (Under her arm was painful) outcome was unknown. No concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Menopause
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 17.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Dysgeusia
Headache
Nausea
Pain
Symptomtext
Patient pretreated with diphenhydramine. Patient expressed nausea and abdominal cramping along with need to vomit. Cramping and nausea subsided by 09:29am. Patient treated with diphenhydramine 25mg/10ml cup. Patient ate package of graham crackers to subside nausea. Expressed metallic taste in mouth. Patient notes GI side effects have subsided but now has headache at 9:33am- pain at a 5 on a scale of 1-10 with 10 being worst. Patient monitored until 9:46am with no other noted effects. Patient provided 4x10ml diphenhydramine cups (25mg/10ml, NDC 68084-0024-59, Lot 502935, EXP 02/28/22)upon discharge from clinic
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None noted
- Vorgeschichte
- None noted
- Andere Medikamente
- None noted
- Allergien
- None noted
- Vorherige Impfungen
- COVID first dose
- Staat
- FL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 12.08.2021
- Impfdatum
- 30.07.2021
- Beginn
- 31.07.2021
- 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
Symptomtext
4-5 inches of redness around injections site
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 07.08.2021
- Impfdatum
- 09.07.2021
- Beginn
- 10.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Headache
Symptomtext
Patient experienced fatigue and headache for 3 days after immunization that went away, but has had a recurring headache also ever since that feels different from headache she may have had prior to vaccination, and was not having recurring headaches prior to vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- acetaminophen, penicillin, morphine
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 06.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Dysgeusia
Hyperhidrosis
Symptomtext
patient experienced immediate dizziness, sweating and strange metallic taste in the back of his mouth
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- none at this tim
- Aktuelle Erkrankungen
- Shortness of Breath. Was scene by Pulmonologist .
- Vorgeschichte
- none
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 05.08.2021
- Impfdatum
- 16.07.2021
- Beginn
- 16.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site rash
Symptomtext
Rashes on the inner left arm close to injectiion site and patient has being using rubbing alcohol
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- -
- Andere Medikamente
- BENADRYL AND RUBBING ALCOHOL PER PT
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 02.08.2021
- Impfdatum
- 29.07.2021
- Beginn
- 30.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test
Dizziness
Dysarthria
Headache
Magnetic resonance imaging
Vision blurred
Symptomtext
Patient called pharmacy 07/30/21 with dizziness, headache, slurred speech and blurred vision. Pharmacy technician was on phone with patient while the pharmacist called 911. He was then hospitalized.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Patient stated he had blood work and MRI's
- Aktuelle Erkrankungen
- he stated no previous illness
- Vorgeschichte
- diabetic heart disease
- Andere Medikamente
- Zanaflex 4mg, Jardiance 10mg, Tresiba 200mg, Losartan 100mg, prozac 20mg, metformin 1000mg, amlodipine 10mg, coreg 12.5mg, ibuprofen 800mg,
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 29.07.2021
- Impfdatum
- 21.07.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
Fatigue
Heart rate increased
Symptomtext
Patient stated that the day after the shot she had extreme fatigue and she went to take a breathing treatment her pulse started going up. Patient was transferred to hospital by Ambulance. She was given blood thinners.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma COPD
- Andere Medikamente
- Nexium Azo bladder control sodium Patient has other medication. could not understand what she was saying .
- Allergien
- Peniclin Iodine Sulfur Morphine Latex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 28.07.2021
- Impfdatum
- 29.06.2021
- Beginn
- 30.06.2021
- 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 lower
Dyspepsia
Injection site erythema
Symptomtext
Site: Redness at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain lower
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 16.07.2021
- Impfdatum
- 16.07.2021
- Beginn
- 16.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Nausea
Symptomtext
pt has dizziness and nausea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 14.07.2021
- Impfdatum
- 13.07.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site haemorrhage
Symptomtext
Pt reports arm still bleeding a small amount at injection site 24 hours post injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site haemorrhage
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 14.07.2021
- Impfdatum
- 14.07.2021
- Beginn
- 14.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Immediate post-injection reaction
Nausea
Symptomtext
Pt received 1st dose of moderna vaccine and immediately reported nausea. Patient reported feeling dizziness after previous vaccinations so pharmacist was planning for observation time of 30 minutes regardless. After current vaccination, pt immediately reported nausea and then shortly after dizziness, pt was sitting down for observation time of 30 minutes and reported feeling ok before going home with her partner.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 14.07.2021
- Impfdatum
- 14.07.2021
- Beginn
- 14.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature decreased
Feeling hot
Hyperhidrosis
Nausea
Symptomtext
About 2 seconds after Moderna vaccine was given to patient, pt reported he was going to vomit. Pt was provided with a bucket to vomit if needed but did not end up doing so. Pt experienced physical sweating and was given some paper towels at his request. Pt denied ice pack at this time. About 3 minutes passed, symptoms subsided and patient was able to articulate what happened. Patient states he felt a major drop in temp. to freezing and then all of a sudden to boiling thus experiencing nausea. Pharmacist kept pt on observation for a 30 minute waiting time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 13.07.2021
- Impfdatum
- 25.06.2021
- Beginn
- 25.06.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Urticaria
Symptomtext
Extreme soreness throughout body, 3 days duration Hives I'm multiple areas, unresolved with over the counter allergy medicine, 2 week duration (ongoing)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Buspar, 30 mg per day Trileptal, 900 mg per day
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 13.07.2021
- Impfdatum
- 13.07.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Dizziness
Nausea
Symptomtext
Patient became dizzy, weak and woozy/nauseous. He reported that he may have passed out for a quick moment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Blood pressure taken 115/78 on 7/13/2021
- Aktuelle Erkrankungen
- None given
- Vorgeschichte
- None given
- Andere Medikamente
- None given
- Allergien
- None given
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 13.07.2021
- Impfdatum
- 12.07.2021
- Beginn
- 13.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Pruritus
Rash macular
Urticaria
Symptomtext
Patient called this morning. He said he had raised red, itchy blotches all over. He said he had some benadryl at home and was going to take some. I followed up with him just now at 3pm. he said the welts have gone down and he's not as itchy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- seasonal allergies worse this year- runny nose, sneezing, cough
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 20.12.2023
- Impfdatum
- 13.09.2021
- Beginn
- 25.10.2023
- Tage bis Beginn
- 772,0
- Dosis
- 2
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breakthrough COVID-19
Symptomtext
Covid-19 Breakthrough Infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breakthrough COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Syncope, HTN, DM, Renal Artery Stenosis, Coronary Artery Disease. AFIB
- Andere Medikamente
- Acetaminophen, Aspirin, Buspirone, Carvedilol, Cholestyramine, Duloxetine, Levetiracetam, Lisinopril, Melatonin, Nirmatrelvir-ritonavir, Ondansetron, Pantoprazole, Sotalol, Spironolactone, Sucralfate
- Allergien
- Codeine, PCN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 05.12.2023
- Impfdatum
- 22.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Autoimmune thyroiditis
Dyspepsia
Hypothyroidism
Symptomtext
hypothyroidism; Hashimotos; Digestive issues; This spontaneous case was reported by a patient and describes the occurrence of HYPOTHYROIDISM (hypothyroidism) and AUTOIMMUNE THYROIDITIS (Hashimotos) in a 73-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 052E21A and 045C21A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 22-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In 2021, the patient experienced HYPOTHYROIDISM (hypothyroidism) (seriousness criterion medically significant), AUTOIMMUNE THYROIDITIS (Hashimotos) (seriousness criterion medically significant) and DYSPEPSIA (Digestive issues). At the time of the report, HYPOTHYROIDISM (hypothyroidism), AUTOIMMUNE THYROIDITIS (Hashimotos) and DYSPEPSIA (Digestive issues) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided. Patient got two shots. They have had health problems ever since they got the vaccines. Caller has Hashimotos, hypothyroidism, digestive issues. Hashimotos was an autoimmune disease and it's destroyed his immune system. Caller says it was about a month later after their second dose, they had their usual 6 month check ups and they had all kinds of new stuff. Company comment: This spontaneous case concerns a 73-year-old male patient, with no medical history reported, who experienced the unexpected, serious (medically significant) events of autoimmune thyroiditis (AESI) and hypothyroidism after receiving the dose of mRNA-1273 vaccine which was described as 2nd dose in Covid-19 vaccination schedule. Latency cannot be calculated due to events onset dates unknown. 1st dose of Covid vaccination schedule was performed with mRNA-1273 with interval between 1st and 2nd dose of 27 days apart. It was reported that events were diagnosed app. a month after the second dose during the usual biannual health check-up. No further details regarding clinical course, etiologic and diagnostic work-up and treatment are available for the review. Events outcome was not resolved at the time of the report. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Autoimmune thyroiditis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 24.08.2023
- Impfdatum
- 05.05.2023
- Beginn
- 23.08.2023
- Tage bis Beginn
- 110,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against and then tested positive for COVID19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 08.08.2023
- Impfdatum
- 07.09.2021
- Beginn
- 08.01.2023
- Tage bis Beginn
- 488,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breakthrough COVID-19
Symptomtext
Breakthrough Covid Infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breakthrough COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Documentation not provided
- Andere Medikamente
- Not listed
- Allergien
- Not listed
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 21.06.2023
- Impfdatum
- 11.09.2021
- Beginn
- 07.06.2022
- Tage bis Beginn
- 269,0
- 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 3/7/21 lot 015M20A; Moderna 4/5/21 lot 025B21A; Moderna 9/11/21 lot 045C21A.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 13.06.2023
- Impfdatum
- 28.09.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 68,0
- Dosis
- 2
- 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 2 vaccines Moderna 8/23/21 lot# 007B21A; Moderna 9/28/21 lot# 045C21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 02.03.2023
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 01.03.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 28.02.2023
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 28.02.2023
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 28.02.2023
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 28.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 28.02.2023
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 28.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 28.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 27.02.2023
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 27.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 27.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 27.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 27.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 100,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 27.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 27.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 27.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 27.02.2023
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 20.10.2021
- Beginn
- 20.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 24.02.2023
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 69,0
- Geschlecht
- U
- Eingang
- 24.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 31,0
- Geschlecht
- U
- Eingang
- 24.02.2023
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 24.02.2023
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 20.10.2021
- Beginn
- 20.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 23.02.2023
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 23.02.2023
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 61,0
- Geschlecht
- U
- Eingang
- 23.02.2023
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 18,0
- Geschlecht
- U
- Eingang
- 23.02.2023
- Impfdatum
- 20.10.2021
- Beginn
- 20.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 59,0
- Geschlecht
- U
- Eingang
- 23.02.2023
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 36,0
- Geschlecht
- U
- Eingang
- 23.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 17.02.2023
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 17.02.2023
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 16.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 16.02.2023
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 16.02.2023
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of the vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 16.02.2023
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of the vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 16.02.2023
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Accidental improper storage of vaccine leading to temperature excursion prior to vaccine administration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 03.01.2023
- Impfdatum
- 11.11.2021
- Beginn
- 21.12.2022
- Tage bis Beginn
- 405,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Hypoxia
Metabolic encephalopathy
SARS-CoV-2 test positive
Sepsis
Symptomtext
Patient received Moderna COVID vaccine on 3/17/21 (lot # 008B21-2A), 4/14/21 (lot # 036B21A), and 11/11/21 (lot # 045C21A). On 12/21/22, patient admitted to our inpatient facility (med/surg unit) with sepsis (HCC) due to COVID infection and possible aspiration pneumonia, hypoxia due to COVID-19 infection, and acute metabolic encephalopathy in setting of infection. Patient was discharged home on 12/25/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 4,0
- Labordaten
- COVID status positive 12/22/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- history of baseline right eye blindness and right-sided weakness due to primary CNS lymphoma (2019) s/p chemotherapy, NIDDM2, HTN, and HLD
- Andere Medikamente
- baby aspirin, atorvastatin, cetirizine, vitamin d3, finasteride, metformin, metoprolol er, tamsulosin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 10.02.2022
- Beginn
- 27.12.2022
- Tage bis Beginn
- 320,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient vaccinated against then tested positive for COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 27.12.2022
- Impfdatum
- 20.09.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administration interrupted
Symptomtext
No adverse event; Patient had original Moderna Covid 19 vaccination on 20-Sep-2021 (O4SC21A), want to inquire if patient need a second dose or just a booster/was told the 2nd dose of Moderna Covid vaccine is no longer available; This spontaneous case was reported by a consumer and describes the occurrence of PRODUCT ADMINISTRATION INTERRUPTED (Patient had original Moderna Covid 19 vaccination on 20-Sep-2021 (O4SC21A), want to inquire if patient need a second dose or just a booster/was told the 2nd dose of Moderna Covid vaccine is no longer available) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 20-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 20-Sep-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced PRODUCT ADMINISTRATION INTERRUPTED (Patient had original Moderna Covid 19 vaccination on 20-Sep-2021 (O4SC21A), want to inquire if patient need a second dose or just a booster/was told the 2nd dose of Moderna Covid vaccine is no longer available). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, PRODUCT ADMINISTRATION INTERRUPTED (Patient had original Moderna Covid 19 vaccination on 20-Sep-2021 (O4SC21A), want to inquire if patient need a second dose or just a booster/was told the 2nd dose of Moderna Covid vaccine is no longer available) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for PRODUCT ADMINISTRATION INTERRUPTED (Patient had original Moderna Covid 19 vaccination on 20-Sep-2021 (O4SC21A), want to inquire if patient need a second dose or just a booster/was told the 2nd dose of Moderna Covid vaccine is no longer available). No concomitant medication information was provided. No treatment medication were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 29.08.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
This spontaneous case was reported by a nursing assistant and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (1 patient expired Moderna dose/2 patients expired Moderna dose) and NO ADVERSE EVENT (No adverse event) in an 88-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 25-Jan-2022 at 2:00 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 25-Jan-2022 at 2:00 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (1 patient expired Moderna dose/2 patients expired Moderna dose). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (1 patient expired Moderna dose/2 patients expired Moderna dose) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related and EXPIRED PRODUCT ADMINISTERED (1 patient expired Moderna dose/2 patients expired Moderna dose) to have an unknown relationship. It was unknown whether patient took over the counter medications, dietary supplements, or herbal remedies being taken at time of vaccination and/or at the time of the adverse event. It was unknown whether the patient ever been diagnosed with tested/positive for Covid-19. It was unknown whether the patient had acute illnesses at the time of vaccination and up to one month before. It was unknown whether the patient had chronic or long standing health conditions. The event did not cause the patient to seek medical care. It was unknown whether the patient had any other potential cause. It was unknown whether the patient experienced a similar event in the past. No treatment medication was provided. This case was linked to US-MODERNATX, INC.-MOD-2022-635425, US-MODERNATX, INC.-MOD-2022-635428 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 25-Aug-2022: Significant follow-up received included updated report type, reporter details added, patient details added, dosage information updated, event onset date added, narrative updated. Sender's Comments: US-MODERNATX, INC.-MOD-2022-635425:88 year old male. US-MODERNATX, INC.-MOD-2022-635428.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 10.08.2022
- Impfdatum
- 20.08.2021
- Beginn
- 28.04.2022
- Tage bis Beginn
- 251,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
Patient was hospitalized with COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension, urinary retention
- Andere Medikamente
- lisinopril, flomax, proscar
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 29.09.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 44,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
Patient received First vaccine dose of the Moderna COVID-19 on the 29 Sep 2021 and second dose on 12 Nov 2021; This spontaneous case was reported by an other health care professional and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received First vaccine dose of the Moderna COVID-19 on the 29 Sep 2021 and second dose on 12 Nov 2021) in a 35-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 076C21A and 045C21A) for COVID-19 prophylaxis. The patient had no allergies to medications, food and other products. The patient had no medical history related to mentioned adverse event and both acute and chronic illnesses at the time of vaccination. The patient had not received any other vaccine within 1 month prior to administration of Moderna COVID-19 vaccine. It was unknown whether the patient was ever tested positive or diagnosed with COVID-19 or not. On 29-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 12-Nov-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received First vaccine dose of the Moderna COVID-19 on the 29 Sep 2021 and second dose on 12 Nov 2021). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received First vaccine dose of the Moderna COVID-19 on the 29 Sep 2021 and second dose on 12 Nov 2021) 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. This case was linked to MOD-2022-615335 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no allergies to medications, food and other products. The patient had no medical history related to mentioned adverse event and both acute and chronic illnesses at the time of vaccination. The patient had not received any other vaccine within 1 month prior to administration of Moderna COVID-19 vaccine. It was unknown whether the patient was ever tested positive or diagnosed with COVID-19 or not.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- -
- Geschlecht
- M
- Eingang
- 02.08.2022
- Impfdatum
- 29.09.2021
- Beginn
- 27.07.2022
- Tage bis Beginn
- 301,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vial initially stored on 01-Jun-2022 and then administered on 27-Jul-2022; administer the vaccine from a vial that was open on 1Jun2022 to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administer the vaccine from a vial that was open on 1Jun2022 to patient) and PRODUCT STORAGE ERROR (Vial initially stored on 01-Jun-2022 and then administered on 27-Jul-2022) in a 35-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 046L21A, 045C21A and 076C21A) for COVID-19 prophylaxis. No Medical History information was reported. On 29-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 27-Jul-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 27-Jul-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (administer the vaccine from a vial that was open on 1Jun2022 to patient). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial initially stored on 01-Jun-2022 and then administered on 27-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administer the vaccine from a vial that was open on 1Jun2022 to patient) and PRODUCT STORAGE ERROR (Vial initially stored on 01-Jun-2022 and then administered on 27-Jul-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient did not tested positive for COVOD-19. No medical history reported relating to mentioned AE and both Acute and Chronic illnesses at the time of vaccination. No other vaccines given within 1 month prior to Moderna COVID-19 vaccine. Dose administered after 30-day Use By Date or after manufacturer date of expiry. No concomitant medication was reported. Date the vial was initially stored in the refrigerator on 1-Jun-2022. HCP administered the vaccine from a vial that was open on 1-Jun-2022 to 6 patients. The vial did not undergo any temperature excursions. No treatment information was reported. This case was linked to MOD-2022-615628 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 31.07.2022
- Impfdatum
- 23.11.2021
- Beginn
- 30.06.2022
- Tage bis Beginn
- 219,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphasia
COVID-19
Gastrointestinal sounds abnormal
Hypokinesia
Oedema peripheral
Pallor
Rales
SARS-CoV-2 test positive
Skin warm
Terminal state
Symptomtext
Patient tested positive for Covid-19 on 06/30/2022 at the Hospital. Patient was then accepted to hospice on 07/02/2022. Patient arrived to hospital via ambulance from hospital accompanied by EMT's. Patient presented nonverbal, decreased, negative purposeful movement, lungs with rales throughout, abdomen soft with hypoactive bowel sounds, skin hot to the touch and pale, left and right hands with 3+ edema, 4LNC of O2. Patient presented actively dying. Terminal diagnosis at facility was Covid-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aphasia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- 20.11.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test
Symptomtext
COVID-19; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (COVID-19) in a 34-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. Concomitant products included DIPHENHYDRAMINE HYDROCHLORIDE, PARACETAMOL (TYLENOL SEVERE ALLERGY) from 17-May-2022 to 24-May-2022 for an unknown indication. On 20-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced COVID-19 (COVID-19). In May 2022, COVID-19 (COVID-19) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In May 2022, SARS-CoV-2 test: negative (Negative) Negative. The patient was taking other medications/products within 2 weeks of starting COVID-19 treatment. The patient previously received a COVID-19 Vaccine. Patient received treatment for COVID-19 with unspecified Pfizer drug from 19-May-2022 to 24-May-2022. It was reported that patient had COVID Rebound on 06-Jun-2022 (12 days after testing negative of COVID). Device Date :06-Jun-2022. Company Comment: This spontaneous case reported by a patient concerns a 34-year-old male patient, with no reported medical history, who experienced unexpected, non-serious AESI Covid19 on an unknown date after vaccination with a third dose of mRNA-1273. Approximately 6 months post-vaccination, he received treatment for Covid19 with an unspecified Pfizer drug. Around 12 days later, he had rebound Covid infection. The ongoing Covid19 pandemic could be a contributory factor. The benefit risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case reported by a patient concerns a 34-year-old male patient, with no reported medical history, who experienced unexpected, non-serious AESI Covid19 on an unknown date after vaccination with a third dose of mRNA-1273. Approximately 6 months post-vaccination, he received treatment for Covid19 with an unspecified Pfizer drug. Around 12 days later, he had rebound Covid infection. The ongoing Covid19 pandemic could be a contributory factor. The benefit risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202205; Test Name: COVID-19 test; Test Result: Negative ; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- TYLENOL SEVERE ALLERGY
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 01.12.2021
- Beginn
- 05.05.2022
- Tage bis Beginn
- 155,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Inappropriate schedule of product administration
Symptomtext
2nd dose was administered more than 42 days after the first dose; Expired 2nd dose administered to patient/patient received expired 2nd dose of Moderna; This spontaneous case was reported by a nurse and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose was administered more than 42 days after the first dose) and EXPIRED PRODUCT ADMINISTERED (Expired 2nd dose administered to patient/patient received expired 2nd dose of Moderna) in a 21-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 012F21A and 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Dec-2021, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 05-May-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 05-May-2022, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose was administered more than 42 days after the first dose) and EXPIRED PRODUCT ADMINISTERED (Expired 2nd dose administered to patient/patient received expired 2nd dose of Moderna). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose was administered more than 42 days after the first dose) and EXPIRED PRODUCT ADMINISTERED (Expired 2nd dose administered to patient/patient received expired 2nd dose of Moderna) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. The reporter stated that the expiration date was from CDC. According to CDC expiration date 19 Mar 2022 was the last updated on this lot. No treatment medications was reported. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 29.04.2022
- Impfdatum
- 27.08.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 127,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Nasopharyngitis
SARS-CoV-2 test positive
Symptomtext
I had COVID-19 in 01/2022 and it was similar to a bad cold. I took Tylenol and my doctor prescribed me steroids and I was feeling better after that. I didn't actually see my doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID-19 test (01/2022)
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- COPD Arthritis
- Andere Medikamente
- Trulicity 3mg/0.5 Lisinopril 30mg Glimepiride 4mg Folic Acid 1mg Lovastatin 20mg Indapamide 1.25mg Methotrexate 2.5mg Diltiazem 180mg75mg Clopidogrel 0.75mg Loratadine 10mg Aspirin 81mg Metformin 1000mg Trazodone 50mg Trelegy 100mg/62.5 Al
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 11.04.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
covid Booster vaccine was given earlier before change in CDC guidance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
covid Booster vaccine was given earlier before change in CDC guidance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 11.04.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
covid Booster vaccine was given 5 days earlier before change in CDC guidance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Type 2 Diabetes, liver function abnormality, gallstones ,Hyperthyroidism
- Andere Medikamente
- metformin HCI ER 500mg
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
COVID-19 booster vaccine given 5 days earlier before change in guidance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Gallstones
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 25.03.2022
- 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: ja
Expired product administered
Symptomtext
Patient received the Moderna booster from this lot 045C21A 15 days after the lot was expired. Patient was advised to return to the clinic for repeat booster as soon as possible.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
Patient received a vaccine from a lot that had expired 15 days previously. Patient advised to RTC ASAP for repeat booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- na
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 30.09.2021
- Beginn
- 16.10.2021
- Tage bis Beginn
- 16,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Metabolic encephalopathy
Speech disorder
Symptomtext
Patient presented to the ED and was subsequently hospitalized for speech disturbance, metabolic encephalopathy within 6 weeks of receiving covid vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Metabolic encephalopathy
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 17,0
- Geschlecht
- U
- Eingang
- 08.03.2022
- Impfdatum
- 08.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- 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
There were no adverse events. The patient wasn't in the approved age group for Moderna booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 07.07.2021
- Beginn
- 08.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site erythema
Vaccination site swelling
Symptomtext
Redness at injection site; swelling at injection site; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE ERYTHEMA (Redness at injection site) and VACCINATION SITE SWELLING (swelling at injection site) in a 34-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No medical history was provided by the reporter. Concomitant products included LISINOPRIL for ACE inhibitor fetopathy. On 07-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Jul-2021, the patient experienced VACCINATION SITE ERYTHEMA (Redness at injection site) and VACCINATION SITE SWELLING (swelling at injection site). At the time of the report, VACCINATION SITE ERYTHEMA (Redness at injection site) and VACCINATION SITE SWELLING (swelling at injection site) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No treatment medications were provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- LISINOPRIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
We gave 1 shot of Moderna 3rd dose to a 16 year old. Moderna is only approved for 18 and above.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 12.11.2021
- Beginn
- 24.01.2022
- Tage bis Beginn
- 73,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
BREAKTHROUGH COVID INFECTION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- 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 Covid-19 vaccine administered to unauthorized age group. Patient was only 17 years of age. No reactions or symptoms to report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Gonorrhea
- Vorgeschichte
- None
- Andere Medikamente
- Rocephin, Pyridoxine, Prenatal Plus
- Allergien
- Delsuym
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 09.09.2021
- Beginn
- 18.01.2022
- Tage bis Beginn
- 131,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Positive for COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 21.09.2021
- Beginn
- 01.02.2022
- Tage bis Beginn
- 133,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Positive COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 14.09.2021
- Beginn
- 05.02.2022
- Tage bis Beginn
- 144,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anticoagulant therapy
COVID-19
Cardiac assistance device user
Fall
Infection
SARS-CoV-2 test positive
Wheelchair user
Wheezing
Symptomtext
Came to ED 2/5/22 Patient was attempting to transfer from the toilet to his wheelchair when he fell. Patient denies dizziness, syncope, headache, nausea or vomiting. He states that the wheelchair slipped out from under him. He denies hitting his head. Patient has a LifeVest in place and states he is waiting an internal defibrillator however he "keeps getting infections. ". Patient is anticoagulated on Eliquis. Patient tested positive for COVID prior to hospitalization, wheezing noted bilaterally. Discharged 2/9/22 - remained on room air and did not require steriods. Previously vacc Moderna 1/7/21, 2/5/21, 9/14/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anticoagulant therapy
- Hospital-Tage
- 4,0
- Labordaten
- COVID PCR + 02/05/2021
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Stage 3 kidney disease, a-fib, CAD, diabetes, DVT, MI, HLD, HTN, multiple myeloma on chemotherapy, anemia
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
Per the CDC definition, patient is not severely immunocompromised. Patient received a third Moderna COVID vaccine dose of 0.5 mL, instead of the standard 0.25 mL. Patient contacted PCP on 1/28/2022; no adverse reactions were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- chronic bronchitis heart murmur history of malignant neoplasm of colon hypertensive disorder neuropathic pain premature atrial contraction ventricular premature beats
- Vorgeschichte
- chronic bronchitis heart murmur history of malignant neoplasm of colon hypertensive disorder neuropathic pain premature atrial contraction ventricular premature beats
- Andere Medikamente
- albuterol sulfate aspirin digoxin diltiazem HCl doxycycline hyclate gabapentin lorazepam Symbicort Trelegy Ellipta
- Allergien
- penicillins
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
Patient was given her third COVID vaccine and received 0.5 mL (dose given to severely immunocompromised patients, as defined by CDC), instead of the standard 0.25 mL dose. No adverse reactions noted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- cellulitis of lower limb (right) cirrhosis of liver congestive heart failure diabetes mellitus gastroesophageal reflux disease nicotine dependence obesity wound
- Vorgeschichte
- cellulitis of lower limb (right) cirrhosis of liver congestive heart failure diabetes mellitus gastroesophageal reflux disease nicotine dependence obesity wound
- Andere Medikamente
- Accu-Chek Guide Me Glucose Mtr Accu-Chek Guide test strips Accu-Chek Softclix Lancets amoxicillin aripiprazole atorvastatin Augmentin BD Ultra-Fine Short Pen Needle benazepril carisoprodol cephalexin Chantix Starting Month Box clobetasol cl
- Allergien
- sulfa; plastic tape; milk; eggs
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 07.09.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 35,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Major depression
Treponema test
Treponema test false positive
Treponema test negative
Symptomtext
Major depression. I suffered through a false positive syphilis result from the covid vaccine. I tested positive for syphilis on Oct 12, 2021 . Reactive (STS) 1:16 DILS. Test result was reported to the health department on October 15, 2021. I was not informed of this lab result January 14, 2022 when I reported to the Department of Health to repeat the syphilis blood test. I had the blood test done on January 14, 2022 I had a FTA-ABs syphilis biological test done which gave a negative result: Non Reactive FTA-ABS. NON-Reactive. Test result was on January 20, 2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Major depression
- Hospital-Tage
- -
- Labordaten
- Blood serology test for syphilis October 12, 2021 Positive reactive test reported October 15, 2021 to the Health Department FTA-ABS blood test done January 14, 2022 Negative syphilis test reported on January 20, 2022
- Aktuelle Erkrankungen
- High blood pressure High cholesterol Hypothyroidism Fatty liver Pre diabetic Osteoarthritis Migraine Stenosis carotid artery
- Vorgeschichte
- High blood pressure, High cholesterol Carotid artery stenosis Hypothyroidism
- Andere Medikamente
- Diovan 320/25 Synthriod 100 Crestor 40 Lamictal 100 twice a day Buscar 10 Aspirin 82 Vitamin D 5000 Maxalt Azulfadine 500
- Allergien
- Demerol Phelnelgan Morphine
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 17.09.2021
- Beginn
- 25.01.2022
- Tage bis Beginn
- 130,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Covid positive through work contact. Not due for booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 11.08.2021
- Beginn
- 17.01.2022
- Tage bis Beginn
- 159,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Productive cough
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
PRODUCTIVE COUGH, RHINORRHEA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- POSITIVE COVID TEST 1/17/2022
- Aktuelle Erkrankungen
- 7/15/21 FAILURE TO THRIVE IN ADULT. WEAKNESS, BLOOD SUGAR PROBLEM
- Vorgeschichte
- Anemia in chronic renal disease CKD (chronic kidney disease) stage 4, GFR 15-29 ml/min Depression ESRD (end stage renal disease) on dialysis Failure to thrive in adult Gout Hypocalcemia Hypertension Immunosuppression Methamphetamine abuse Organ transplant- kidney, liver Tobacco abuse Type II diabetes mellitus Vitamin D deficiency
- Andere Medikamente
- Carvedilol (Coreg) 25 Mg Tablet Cholecalciferol (Vitamin D3) 25 Mcg (1000 Units) Capsule Insulin Pen Needle 31G X 8 Mm Insulin Aspart (Novolog) 100 Units/Ml Subcutaneous Flexpen Metformin (Glucophage-xr) 500 Mg 24 Hr Tablet Mycophe
- Allergien
- Ibuprofen Nsaids (Non-Steroidal Anti-Inflammatory Drug)
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 06.11.2021
- Beginn
- 17.01.2022
- Tage bis Beginn
- 72,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
HOSPITALIZATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 10.09.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 103,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested Positive for Covid
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- Impfdatum
- 21.07.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 161,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Covid positive contact unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 19.07.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 163,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
Nasal congestion
SARS-CoV-2 test positive
Symptomtext
Tested positive with mild symptoms, stuffy nose and cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
She received her booster of the Moderna vaccine/ received a dose from a lot that might have been improperly stored; This spontaneous case was reported by a consumer and describes the occurrence of PRODUCT STORAGE ERROR (She received her booster of the Moderna vaccine/ received a dose from a lot that might have been improperly stored) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-Oct-2021, the patient experienced PRODUCT STORAGE ERROR (She received her booster of the Moderna vaccine/ received a dose from a lot that might have been improperly stored). On 27-Oct-2021, PRODUCT STORAGE ERROR (She received her booster of the Moderna vaccine/ received a dose from a lot that might have been improperly stored) had resolved. No relevant concomitant medications were reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product temperature excursion issue
Symptomtext
given shots during excursions; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (given shots during excursions) in a 56-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 27-Oct-2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (given shots during excursions). On 27-Oct-2021, PRODUCT TEMPERATURE EXCURSION ISSUE (given shots during excursions) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication information was provided. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product temperature excursion issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product temperature excursion issue
Symptomtext
Product temperature excursion issue; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Product temperature excursion issue) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 29-Oct-2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Product temperature excursion issue). On 29-Oct-2021, PRODUCT TEMPERATURE EXCURSION ISSUE (Product temperature excursion issue) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product temperature excursion issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 25.12.2021
- Impfdatum
- 12.10.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product temperature excursion issue
Symptomtext
Patients were given shots during excursions; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Patients were given shots during excursions) in an 85-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 065F21A and 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 ml. On 09-Nov-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .5 ml. On 09-Nov-2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Patients were given shots during excursions). On 09-Nov-2021, PRODUCT TEMPERATURE EXCURSION ISSUE (Patients were given shots during excursions) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication reported. No treatment information provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product temperature excursion issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product temperature excursion issue
Symptomtext
patients were given shots during excursions; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT STORAGE ERROR (patients were given shots during excursions) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .25 milliliter. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 28-Oct-2021, the patient experienced PRODUCT STORAGE ERROR (patients were given shots during excursions). On 28-Oct-2021, PRODUCT STORAGE ERROR (patients were given shots during excursions) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant drugs were reported. No treatment drugs were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product temperature excursion issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product temperature excursion issue
Symptomtext
patients were given shots during excursions.; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (patients were given shots during excursions.) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 ml. On 02-Nov-2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (patients were given shots during excursions.). On 02-Nov-2021, PRODUCT TEMPERATURE EXCURSION ISSUE (patients were given shots during excursions.) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant products were not provided. Treatment medication were not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product temperature excursion issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 25.12.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product temperature excursion issue
Symptomtext
patients were given shots during excursions; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (patients were given shots during excursions) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 27-Oct-2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (patients were given shots during excursions). On 27-Oct-2021, PRODUCT TEMPERATURE EXCURSION ISSUE (patients were given shots during excursions) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication information was reported. No treatment medications were provided This case was linked to MOD-2021-423303 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product temperature excursion issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product temperature excursion issue
Symptomtext
Patients were given shots during excursions.; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Patients were given shots during excursions.) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 16-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .25 ml. 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 16-Nov-2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Patients were given shots during excursions.). On 16-Nov-2021, PRODUCT TEMPERATURE EXCURSION ISSUE (Patients were given shots during excursions.) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications information was not reported No treatment medications were provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product temperature excursion issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product temperature excursion issue
Symptomtext
Product temperature excursion issue; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Product temperature excursion issue) in a 79-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 02-Nov-2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Product temperature excursion issue). On 02-Nov-2021, PRODUCT TEMPERATURE EXCURSION ISSUE (Product temperature excursion issue) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant Drug details were reported. No Treatment information was provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product temperature excursion issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 25.12.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product temperature excursion issue
Symptomtext
patients were given shots during excursions.; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (patients were given shots during excursions.) in a 66-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 28-Oct-2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (patients were given shots during excursions.). On 28-Oct-2021, PRODUCT TEMPERATURE EXCURSION ISSUE (patients were given shots during excursions.) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications reported by reporter No treatment medications provided by the reporter. This case was linked to MOD-2021-423403 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product temperature excursion issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 93,0
- Geschlecht
- M
- Eingang
- 25.12.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product temperature excursion issue
Symptomtext
Product temperature excursion issue/patients were given shots during excursions; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Product temperature excursion issue/patients were given shots during excursions) in a 93-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 28-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 28-Oct-2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Product temperature excursion issue/patients were given shots during excursions). On 28-Oct-2021, PRODUCT TEMPERATURE EXCURSION ISSUE (Product temperature excursion issue/patients were given shots during excursions) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications information was reported. No treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product temperature excursion issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 25.12.2021
- Impfdatum
- 29.09.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 30,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product temperature excursion issue
Symptomtext
Patients were given shots during excursions; This spontaneous case was reported by a health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Patients were given shots during excursions) in a 32-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 ml. On 29-Oct-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .5 ml. On 29-Oct-2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Patients were given shots during excursions). On 29-Oct-2021, PRODUCT TEMPERATURE EXCURSION ISSUE (Patients were given shots during excursions) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant products were not provided. Treatment medications were not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product temperature excursion issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product temperature excursion issue
Symptomtext
Patient was given shots during excursions; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Patient was given shots during excursions) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 27-Oct-2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Patient was given shots during excursions). On 27-Oct-2021, PRODUCT TEMPERATURE EXCURSION ISSUE (Patient was given shots during excursions) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Excursion date was given as 27 Oct 2021. No concomitant drug details were reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product temperature excursion issue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 24.12.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
patients were given shots during excursions; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT STORAGE ERROR (patients were given shots during excursions) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 ml. On 29-Oct-2021, the patient experienced PRODUCT STORAGE ERROR (patients were given shots during excursions). On 29-Oct-2021, PRODUCT STORAGE ERROR (patients were given shots during excursions) had resolved. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant medications were reported. No treatment medications were reported. Excursion dates were reported as 27 October 2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Given moderna booster at age 17
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Loestrin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 07.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Accidental underdose
Symptomtext
patient received half dose of the Moderna vaccine as 1st dose; This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL UNDERDOSE (patient received half dose of the Moderna vaccine as 1st dose) in a 55-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. Concomitant products included FLUTICASONE PROPIONATE, SALMETEROL XINAFOATE (ADVAIR), GLIMEPIRIDE, METFORMIN HYDROCHLORIDE (GLUCOPHAGE), MODAFINIL, MONTELUKAST SODIUM (SINGULAIR), SEMAGLUTIDE (RYBELSUS) and BUMETANIDE for an unknown indication. On 03-Dec-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Dec-2021, the patient experienced ACCIDENTAL UNDERDOSE (patient received half dose of the Moderna vaccine as 1st dose). On 03-Dec-2021, ACCIDENTAL UNDERDOSE (patient received half dose of the Moderna vaccine as 1st dose) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No treatment details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ADVAIR; GLIMEPIRIDE; GLUCOPHAGE; MODAFINIL; SINGULAIR; RYBELSUS; BUMETANIDE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 20.08.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 96,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested Positive for Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 27.11.2021
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
None, patient received 0.25ml dose instead of 0.5ml dose since she is immunocompromised. She called backed 3 weeks after dose. Per CDC guidelines we recommended patient come back and receive 0.5ml dose. Patient has not returned to receive dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- U
- Eingang
- 25.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- 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
administered with the vaccine from a vial punctured for more than 12 hours; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered with the vaccine from a vial punctured for more than 12 hours) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered with the vaccine from a vial punctured for more than 12 hours). On 01-Nov-2021, EXPIRED PRODUCT ADMINISTERED (administered with the vaccine from a vial punctured for more than 12 hours) had resolved. 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.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 23.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Product administration error
Symptomtext
Vaccine Administration Error: The Moderna COVID-19 vaccine is currently authorized under Emergency Use Authorization (EUA) for individuals 18 years and older. The parents registered their 12 year old son to receive a Moderna vaccine at the drive through clinic. The registration form requires individuals to confirm they are 18 years or older, but no hard stops prevent registration if the age requirement is not met. The mother provided consent for the vaccination at the clinic and Moderna vaccine was given to the child in the adult dose of 100 micrograms, 0.5 ml. After the vaccination was given, the staff member recognized an error had been made and that the child was not eligible for the vaccination given.
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
- No known drug allergies
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
IM given in left arm 3rd dose. Moderna COVID-19 vaccine lot 045C21A given was removed from freezer on 10/6/2021 at 11:45 AM. Given on 11/5/2021, out of range. Patient contacted that evening. Moderna manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/21 and let him know that Moderna let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
IM given in left arm 3rd dose (Booster). Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/21 @ 11:45 am. Given on 11/5/21, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard bak from them. Called patient today 11/17/21 and let him know that oderan let us know the vacine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
IM given in left arm 3rd dose. (Booster). Moderna Covid-19 Vaccine Lot 045C21 given was removed from freezer on 10/6/2021 @ 11:45am, Given on 11/5/2021, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/21 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
IM given in left arm 3rd dose. Moderna COVID-19 vaccine Lot 045C21A given was removed from freezer on 10/6/2021 at 11:45 am. Given on 11/5/2021, out of range. Patient contacted that evening. Moderna manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/2021 and let him know that Moderna let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- JET / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
IM given in left arm 3rd dose. (Booster). Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/21 @ 11:45 am. Given on 11/5/21, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/21 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
IM given in left arm 3rd dose. (Booster). Moderna COVID-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/2021 @ 11:45AM. Given on 11/5/2021, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that MODERNA was looking into this and would be getting back to us. Also let them know I would be following up on them once we heard back from them. Called patient today 11/17/2021 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
IM given in left arm 3rd dose. (Booster). Moderna COVID-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/2021 @ 11:45AM. Given on 11/5/2021, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up on them once we heard back from them. Called patient today 11/17/2021 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
IM given in left arm 3rd dose. (Booster). Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/21 at 11:45 am. Given on 11/5/21, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/21 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
IM given in left arm 3rd dose. (Booster). Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/21 @ 11:45 am. Given on 11/5/21, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/2021 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
IM given in left arm 3rd dose. (Booster). Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/21 @ 11:45am. Given on 11/5/21, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/21 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
IM given in left arm 3rd dose. (Booster). Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/201 @ 11:45 am. Given on 11/5/21, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know ow that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/21 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
IM given in left arm 3rd dose. Moderna COVID-19 vaccine lot 045C21A given was removed from freezer on 10/6/2021 at 11:45 am. Given on 11/5/2021, out of time range. Patient contacted that evening. Moderna manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/2021 and let him know that Moderna let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- JET / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
IM given in left arm 3rd dose. (Booster). Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/21 @ 11:45 am. Given on 11/5/21, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/21 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
IM given in left arm 3rd dose. (Booster) Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/2021 @ 11:45 am. Given on 11/5/2021, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up on them once we heard back from them. Called patient today 11/17/2021 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
IM given in left arm 3rd dose. (Booster). Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/21 at 11:45 am. Given on 11/5/21, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/21 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Product storage error
Symptomtext
IM given in left arm 3rd dose. (Booster) Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/2021 @ 11:45 am. Given on 11/5/2021, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up on them once we heard back from them. Called patient today 11/17/2021 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
IM given in left arm 3rd dose. (Booster) Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/2021 @ 11:45 am. Given on 11/5/2021, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up on them once we heard back from them. Called patient today 11/17/2021 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
IM given in left arm 3rd dose. (Booster). Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/21 @ 11:45 am. Given on 11/5/21, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/21 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
IM given in left arm 3rd dose. (Booster). Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/21 at 11:45 am. Given on 11/5/21, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/21 and let him know that Moderan let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
IM given in left arm 3rd dose. (Booster). Moderna Covid-19 vaccine Lot 05C21A given was removed from freezer on 10/6/21 @ 11:45 am. Given on 11/5/21,out of time range. Patient contacted that evening. Moderna manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/21 and let her know that Moderna let us know the vaccine was viable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 11
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IN / NS
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
IM given in left arm 3rd dose, (Booster). Moderna Covid-19 Vaccine Lot 045C21A given was removed from freezer on 10/6/21 @ 11:45 am. Given on 11/5/21, out of time range. Patient contacted that evening. Moderan manufacturer called. Patients called the following Monday letting them know that Moderna was looking into this and would be getting back to us. Also let them know I would be following up with them once we heard back from them. Called patient today 11/17/21 and let him know that Moderan let us know the vaccine was vlable, no additional booster vaccine is required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 14.11.2021
- Beginn
- 14.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dry mouth
Swollen tongue
Symptomtext
Pt received her Moderna booster along with influenza vaccine at the Vaccine event on Sunday 11/14. About 8 minutes after her vaccinations, pt reported feeling dryness of her buccal mucosa, along with sensation of her tongue swelling. Physical exam WNL, airway patent. HR ranging from 60-70's. Lungs clear to auscultation. No signs of respiratory distress or compromise. Pt agreed to taking Benadryl 25mg PO and drinking water. About 10 minutes after Benadryl, pt reported feeling much better, but still with some mucosal dryness. All VSS. Patient alert and oriented. We agreed that pt would seek medical attention if any symptoms worsened.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dry mouth
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 02.09.2021
- Beginn
- 09.10.2021
- Tage bis Beginn
- 37,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Intermenstrual bleeding
Menstruation irregular
Symptomtext
After receiving my first covid vaccination I started my regular menses that lasted approximately 7 days. I then spotted off and on for a week after that. After my 2nd vaccination I started my next scheduled menses which lasted approximately 7 days. A week later, I started another menses that lasted another 7 days. I've never had this happen in 40 years. My menses average about 5 days every 32 days. I feel its directly related to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intermenstrual bleeding
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Reactive Airway, Sciatica pain
- Andere Medikamente
- Multi-vitamin, Tumeric, Vitamin C, Vitamin B12, Gabapentin, and Singular
- Allergien
- Ceclor, Vancomycin, Macrobid, corn, mosquitos
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 02.09.2021
- Beginn
- 09.10.2021
- Tage bis Beginn
- 37,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Intermenstrual bleeding
Menstruation irregular
Symptomtext
After receiving my first covid vaccination I started my regular menses that lasted approximately 7 days. I then spotted off and on for a week after that. After my 2nd vaccination I started my next scheduled menses which lasted approximately 7 days. A week later, I started another menses that lasted another 7 days. I've never had this happen in 40 years. My menses average about 5 days every 32 days. I feel its directly related to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intermenstrual bleeding
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Reactive Airway, Sciatica pain
- Andere Medikamente
- Multi-vitamin, Tumeric, Vitamin C, Vitamin B12, Gabapentin, and Singular
- Allergien
- Ceclor, Vancomycin, Macrobid, corn, mosquitos
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 16.11.2021
- Impfdatum
- 12.02.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 271,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Syringe issue
Symptomtext
Our pharmacy used Mini-Spice Dispending Pin (Braun 412012) to draw up Moderna Vaccine Boosters from 7.5 mL vial After contacting with the manufacturer, we have learned that the 20 dose limit was enacted because puncturing the vial more than 20 times could create an open microbiological pass of the contents of the vial. However, our dispensing pin is sterile . We have punctured the vial only once., thus sterility was not compromised. Having said that, we are submitting this report to alert other hospitals NOT to use Mini-Spike Dispensing Pin to draw up extra doses of vaccine from the same vial. Moderna Guidelines: a vial should not be punctured more than 20 times. Therefore, no more than 20 doses should be obtained form one vial
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syringe issue
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 24.09.2021
- Beginn
- 28.09.2021
- Tage bis Beginn
- 4,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
BREAKTHROUGH COVID INFECTION. PATIENT TESTED POSITIVE ON 09/28/2021. PATIENT WAS FULLY VACCINATED ON 09/24/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- -
- Geschlecht
- F
- Eingang
- 13.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
20 expired booster doses(exp date 4 nov 2021) on 5NOV2021; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED on 5NOV2021 in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 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 05-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED on 5NOV2021. On 05-Nov-2021, EXPIRED PRODUCT ADMINISTERED on 5NOV2021 had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. Most recent FOLLOW-UP information incorporated above includes on 08-Nov-2021 the follow up received contains non significant information, added patient demographics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 13.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- 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
Product storage error
Symptomtext
vaccinated past the 12 hour time frame; a bottle and opened it on 27Oct2021. They left it open in the refrigerator and gave it to possibly 2 patients on 01Nov2021; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED and PRODUCT STORAGE ERROR. They left it open in the refrigerator and gave it to possibly 2 patients on 01Nov2021 in an 85-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. Previously administered products included for COVID-19 vaccination of Pfizer vaccine (first PFIZER COVID-19 vaccination intramuscularly with lot number EN6199) on 09-Mar-2021 and Pfizer vaccine (second PFIZER COVID-19 vaccination with Lot number ER8727) on 25-Mar-2021. Past adverse reactions to the above products included No adverse event with Pfizer vaccine and Pfizer vaccine. Concomitant products included OMEPRAZOLE, LEVOTHYROXINE, LISINOPRIL, and SILDENAFIL for an unknown indication. On 01-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED and PRODUCT STORAGE ERROR (a bottle and opened it on 27Oct2021. They left it open in the refrigerator and gave it to possibly 2 patients on 01Nov2021). On 01-Nov-2021, EXPIRED PRODUCT ADMINISTERED and PRODUCT STORAGE ERROR on 27Oct2021. They left it open in the refrigerator and gave it to possibly 2 patients on 01Nov2021 had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Treatment medications was not specified This case was linked to MOD-2021-370117 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- OMEPRAZOLE; LEVOTHYROXINE; LISINOPRIL; SILDENAFIL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 13.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
vaccinated past the 12 hour time frame; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccinated past the 12 hour time frame) in an 86-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Nov-2021, 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 01-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccinated past the 12 hour time frame). On 01-Nov-2021, EXPIRED PRODUCT ADMINISTERED (vaccinated past the 12 hour time frame) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications was reported. No treatment drug details was reported. This case was linked to MOD-2021-370117 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
Vial expired on 11/4/2021. Notified Pharmacist, no recommendations at this time. No adverse reactions noted from patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Dementia, Down's syndrome, Type 2 diabetes, obesity, hyperlipidemia, hypothyroidism, depression, GERD, PVD, Osteoarthritis, Hearing loss, chronic sinusitis, Ulcerative colitis, Allergic rhinitis, bronchitis, dysphagia, falls
- Andere Medikamente
- Acetaminophen, Aripiprazole 2 mg, Vitamin D3 25mcg, Vitamin B-12, Fluticasone, Levothyroxine 112mcg, Melatonin 5mg, Mesalamine 0.375 gram, MVI, Protonix 20mg, Rosuvastatin 5mg, Tramadol 50mg, Tums, Vitamin A.
- Allergien
- Benadryl, Codeine, Penicillin, Sulfonamides
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Moderna vaccine was administered from a vial having been opened for over 12 hours; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna vaccine was administered from a vial having been opened for over 12 hours) in an 86-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter once. On 01-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna vaccine was administered from a vial having been opened for over 12 hours). On 01-Nov-2021, EXPIRED PRODUCT ADMINISTERED (Moderna vaccine was administered from a vial having been opened for over 12 hours) had resolved. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were provided. 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
- FL
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
Moderna vaccine was administered from a vial having been opened for over 12 hours.; Moderna vaccine was administered from a vial having been opened for over 12 hours.; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (Moderna vaccine was administered from a vial having been opened for over 12 hours.) and EXPIRED PRODUCT ADMINISTERED (Moderna vaccine was administered from a vial having been opened for over 12 hours.) in an 85-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. The patient's past medical history included Erectile dysfunction, Hypothyroidism, Colon operation, Wrist fracture and Gastric ulcer (Over 20 years ago.). Concurrent medical conditions included Hypertension, Diabetes, Hyperlipidemia, Obesity, GERD, Insomnia, Lipoma, After-cataract and Diverticulosis. On 01-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter once. On 01-Nov-2021, the patient experienced PRODUCT STORAGE ERROR (Moderna vaccine was administered from a vial having been opened for over 12 hours.) and EXPIRED PRODUCT ADMINISTERED (Moderna vaccine was administered from a vial having been opened for over 12 hours.). On 01-Nov-2021, PRODUCT STORAGE ERROR (Moderna vaccine was administered from a vial having been opened for over 12 hours.) and EXPIRED PRODUCT ADMINISTERED (Moderna vaccine was administered from a vial having been opened for over 12 hours.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication was reported by the reporter. No treatment information provided. Patient age over 65, Immunocompromised
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- After-cataract; Diabetes; Diverticulosis; GERD; Hyperlipidemia; Hypertension; Insomnia; Lipoma; Obesity
- Vorgeschichte
- Medical History/Concurrent Conditions: Colon operation; Erectile dysfunction; Gastric ulcer (Over 20 years ago.); Hypothyroidism; Wrist fracture
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Was administered Moderna vaccine from a vial having been opened for over 12 hours; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Was administered Moderna vaccine from a vial having been opened for over 12 hours) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. Concurrent medical conditions included Anxiety disorder and Impaired fasting glucose. On 29-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 29-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Was administered Moderna vaccine from a vial having been opened for over 12 hours). On 29-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Was administered Moderna vaccine from a vial having been opened for over 12 hours) had resolved. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. Treatment information was not provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Anxiety disorder; Impaired fasting glucose
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- 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
Symptomtext
Moderna vaccine was administered from open vial of over 12 hours being opened.; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna vaccine was administered from open vial of over 12 hours being opened.) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. The patient's past medical history included Esophageal varices, Pancreatic cancer and Esophagitis. Concurrent medical conditions included Anemia. On 27-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter once. On 27-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna vaccine was administered from open vial of over 12 hours being opened.). On 27-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Moderna vaccine was administered from open vial of over 12 hours being opened.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medication information was not reported Treatment information was not reported
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Anemia; Esophageal varices; Esophagitis; Pancreatic cancer
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 08.11.2021
- Impfdatum
- 14.09.2021
- Beginn
- 30.09.2021
- Tage bis Beginn
- 16,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
second dose of Moderna was administered sooner than the recommended minimum timeframe of 28days. It was administered on day 15. Dose 1 given on 9/14/2021 Dose 2 given on 9/30/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- none at this time. MD reviewed resident for any adverse events and none were identified at time of evaluation.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Bactrim
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
received 0.5ml dose of vaccine instead of the 0.25ml recommended
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 25,0
- Geschlecht
- U
- Eingang
- 04.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
received 0.5ml dose instead of 0.25ml recommended dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Symptomtext
received 0.5ml dose instead of 0.25ml dose recommended
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
received 0.5ml dose instead of 0.25ml recommended dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Symptomtext
0.5ml of the vaccine was administered instead of the 0.25ml recommended dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient was given Moderna vaccine 0.5cc in the right deltoid and she is only 16 years old. Per CDC guidelines, Moderna is administered to individuals age 18 or older. No adverse events after injection. Patient was monitored for 20 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
lymph node swelling
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- morphine
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 12.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Wrong product administered
Symptomtext
Patient received Moderna booster dose (0.25 mL) and was found to have only received one dose in series (Pfizer). Patient was given additional (0.25 mL) Moderna to make full dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 02.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient came in with 2 other female relatives for first covid vaccine dose. Brother acted as interpreter; All women requested Moderna first dose. Brother was required to leave room prior to women being able to expose their arms per family. Pt was vaccinated, however she was discovered to be 17 yrs old after, even though she presented with the paperwork for an adult of age 18.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Unknown; No underlying health conditions
- Vorgeschichte
- No underlying health conditions
- Andere Medikamente
- Unknown
- Allergien
- No medication allergies
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient was given .5ml instead of the recommended .25ml of moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN degenerative Disc
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the recommended dose of .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Unknown
- Andere Medikamente
- unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the recommended .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None recorded
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None recorded. Lives with immunosuppress partner.
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the recommended dose of .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- hypercholesterolemia hypothyroidism
- Andere Medikamente
- unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the recommended .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- hypertensive disorder hyperuricemia knee pain (bilateral) low back pain microscopic hematuria mixed hyperlipidemia osteoarthritis of knee osteoarthritis of left foot osteoarthritis of right knee joint
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the recommended .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the recommended .25ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None recorded
- Andere Medikamente
- Unknown
- Allergien
- Sulfa (Sulfonamide Antibiotics)
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the recommended .25ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 28.10.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the recommended .25ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- environmental allergy fatigue mixed hyperlipidemia multiple environmental allergies pain in right hip joint
- Andere Medikamente
- Unknown
- Allergien
- cat dander dog dander horse dander Water Babies Spf 30
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the recommended .25ml of moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- chronic atrial fibrillation hypertensive disorder
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DM
- Andere Medikamente
- Unknown
- Allergien
- glyburine
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of .25ml of the moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- DM HTN
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient received .5ml instead of the recommended .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient given .5ml instead of the recommended .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- benign essential hypertension hypothyroidism Type 2 diabetes mellitus without complication
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient was given .5ml instead of the recommended .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the recommended .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- dysthymia bilateral tinnitus
- Andere Medikamente
- unknown
- Allergien
- Flonase
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the recommended .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- acquired hypothyroidism hypertensive disorder
- Andere Medikamente
- unknown
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was given . 5ml instead of the recommended .25ml of moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- carotid artery stenosis congestive heart failure chronic kidney disease stage 3 disorder due to type 2 diabetes mellitus
- Andere Medikamente
- Unknown
- Allergien
- codeine
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Symptomtext
Patient was given .5ml of moderna instead of the recommended .25ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- acute congestive heart failure chronic obstructive lung disease degeneration of lumbar intervertebral disc hypertensive disorder
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 27.10.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administration error
Underdose
Symptomtext
MODERNA COVID-19 VACCINE EUA: The patient was given Moderna 0.25mL IM x 1 instead of Moderna 0.5mL IM x 1 as dose #1 of the primary series. The patient was immediately called in an attempt to inform him of the administration error once it had been identified and also to have the patient return to the clinic for a repeat dose. However, the patient was not able to be contacted, and a voicemail was left requesting call back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administration error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the recommended .25ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Diabetes Hypertension
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of the recommended .25ml.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of .25ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HTN Hyperlipidemia
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Incorrect dose administered
Symptomtext
Patient was given .5ml of the moderna vaccine instead of .25ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Chronic pain
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 27.10.2021
- Impfdatum
- 18.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient was given .5ml of booster instead of .25ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN, CAD
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- 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
Symptomtext
PATIENT RECEIVED BOOSTER DOSE OF MODERNA COVID-19 VACCINE 2 MONTHS EARLY. LAST DOSE OF MODERNA COVID-19 VACCINE WAS 070821 AND BOOSTER DOSE WAS GIVEN 102621.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CHRONIC KIDNEY DISEASE, HTN, HYPERLIPIDEMIA, OBESITY
- Andere Medikamente
- -
- Allergien
- TRAZADONE
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 25.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
No adverse event. Pt received 0.5ml instead 0.25ml for booster dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 25.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Upon arriving at the facility for a COVID booster clinic I was told that Pt needed her 2nd Moderna vaccine. There was only 1 shot documented in the facility's ER. Upon filling out the patient's card (the card could not be located when I started the clinic; it was brought to me towards the end of the clinic), I realized she had already received her 2nd dose on 08/24/2021. Because the patient does not qualify as immunocompromised, giving the 0.5ml of Moderna 2 months after her second shot was an error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 21.10.2021
- Impfdatum
- 11.10.2021
- Beginn
- 11.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
received dose after more than 30 days refrigerated; Based on the current case data, this case has been classified as invalid. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received dose after more than 30 days refrigerated) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (received dose after more than 30 days refrigerated). On 11-Oct-2021, EXPIRED PRODUCT ADMINISTERED (received dose after more than 30 days refrigerated) had resolved. 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 provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 17.10.2021
- Impfdatum
- 03.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
event: Patient present for Covid vaccine and LPN correctly asked patient if he was getting a Moderna vaccine today and he answered, ?yes.? Mom stated to nurse ?I want him to get the Moderna.? Moderna vaccine given and when scheduling for second vaccine, it was noted that he was 17 years old and this vaccine was not indicated. The Director spoke with mom and patient, informing them of error. No adverse reaction noted. Encouraged family to call with any concerns or possible reactions. Also let them know that patient could receive second Moderna vaccine at appropriate time if they so wished. Shared that this is recommendation of CDC. Mom and patient agreed to second Moderna vaccine. Director instructed patient and mom to call with any questions or concerns.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none needed
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- obesity, GERD, Dysphagia, poor hygiene, mild asthma, hisotry of cardiac murmur
- Andere Medikamente
- none known
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 16.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
1st dose administered to 14 year old; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (1st dose administered to 14 year old) in a 14-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Oct-2021, the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (1st dose administered to 14 year old). On 01-Oct-2021, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (1st dose administered to 14 year old) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment medications were provided. Pharmacy accidentally administered a 1st Moderna dose to a 14 year old
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
- 55,0
- Geschlecht
- M
- Eingang
- 13.10.2021
- Impfdatum
- 03.09.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 12.10.2021
- Impfdatum
- 12.10.2021
- Beginn
- 12.10.2021
- 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 a Moderna vaccine and was only 17
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 11.10.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Administration of expired vaccine/vaccine vial that was in the fridge for more than 30 days; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administration of expired vaccine/vaccine vial that was in the fridge for more than 30 days) in a 29-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Oct-2021 at 2:30 PM, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administration of expired vaccine/vaccine vial that was in the fridge for more than 30 days). On 01-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Administration of expired vaccine/vaccine vial that was in the fridge for more than 30 days) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. No treatment information was provided by the reporter. The patient was monitored after Moderna COVID vaccine was administered for 15 min. Pt was ok and left home after 15 min observation. Most recent FOLLOW-UP information incorporated above includes: On 07-Oct-2021: Non- Significant Follow-up received on 07-OCT-2021 contains patient condition (patient was monitored after Moderna Covid vaccine was administered for 15 min. Pt was ok and left home after 15 min observation).
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
- 08.10.2021
- Impfdatum
- 22.09.2021
- Beginn
- 22.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
No adverse event
Symptomtext
Patient first received Moderna COVID vaccine on 2/11/21 and 3/11/21. On 9/22/21, patient received Moderna COVID vaccine dose #3 even though she's not moderately/severely immune suppressed and the criteria used for rationale of giving the patient a third dose was age>65. This is an error as we are not yet giving third booster doses to non immune suppressed patients and Moderna has not been approved for booster doses. No adverse event to the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- benign essential hypertension, h/o psoriasis, restless leg syndrome, raynaud disease
- Andere Medikamente
- Premarin, hydrochlorothiazide, Provera, nifedipine ER
- Allergien
- Bee venom protein
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 07.10.2021
- Impfdatum
- 15.09.2021
- Beginn
- 15.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Platelet count increased
Unresponsive to stimuli
White blood cell count increased
Symptomtext
Unresponsive episode, transferred to local ED via Ambulance. Increased WBC, Platelets Inpatient hospital stay.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Platelet count increased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- C-H-F See List
- Andere Medikamente
- Lovastatin, mvl, miralax, Prednisone, Torsemide, warfarin
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 05.10.2021
- Impfdatum
- 04.10.2021
- Beginn
- 04.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
No adverse event
Symptomtext
Moderna COVID-19 Vaccine EUA inadvertently given instead of Pfizer BioNTech COVID-19 Vaccine EUA. No symptoms appeared during the 15 minute wait time after vaccine administered and currently no other symptoms at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 03.09.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Asthenopia
Computerised tomogram normal
Laboratory test normal
Magnetic resonance imaging normal
Ultrasound Doppler
Vasodilatation
Vision blurred
Symptomtext
Per Patient Report - 'Blurry vision, tired eyes, blood vessles slighty(sic) protruding. Went to urgent care. Sent to ER from urgent care. Had lab work, CT, MRI, All normal results. Followed up with Doctor (sic) and optimatrist (sic) next day. All results normal. Had ultrasound of caritated (sic) arteries. Results normal."
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenopia
- Hospital-Tage
- -
- Labordaten
- Per Patient Report - "labs, CT & MRI 9/7/21, caritarted (sic) arteries ultrasound 9/14/21."
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 01.10.2021
- Impfdatum
- 10.09.2021
- Beginn
- 11.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Swelling of eyelid
Symptomtext
Upper eye lid began to swell.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Swelling of eyelid
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- -
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 28.09.2021
- Impfdatum
- 10.09.2021
- Beginn
- 19.09.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Menstruation delayed
Symptomtext
period delayed for 4 days; This spontaneous case was reported by a consumer and describes the occurrence of MENSTRUATION DELAYED (period delayed for 4 days) in a 40-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. Concurrent medical conditions included Drug allergy (Allergic to Sulfa). On 10-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 19-Sep-2021, the patient experienced MENSTRUATION DELAYED (period delayed for 4 days). At the time of the report, MENSTRUATION DELAYED (period delayed for 4 days) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitants medication were provided. No treatment medication were provided. Second dose is scheduled on 8-Oct-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstruation delayed
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy (Allergic to Sulfa)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
There was an opened unlabeled vial of Moderna in the VFC fridge. There had not been any mentions on the group chat of an open Moderna vial (as when we open each vial we let everyone in the chat know) . I grabbed the open vial along with an unopened vial of Moderna and proceeded to the Covid clinic. There were 7 doses of this vaccine given to patients. As of 9/27 we were off on our counts and now realize that the vial that was used on 9/24 to those 7 patients was an expired vial. The vial had originally been opened on 9/23 by RN. These 7 patients have been located and will be contacted once recommendations from CDC are reviewed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
There was an opened unlabeled vial of Moderna in the VFC fridge. There had not been any mentions on the group chat of an open Moderna vial (as when we open each vial we let everyone in the chat know) . I grabbed the open vial along with an unopened vial of Moderna and proceeded to the Covid clinic. There were 7 doses of this vaccine given to patients. As of 9/27 we were off on our counts and now realize that the vial that was used on 9/24 to those 7 patients was an expired vial. The vial had originally been opened on 9/23 by RN. These 7 patients have been located and will be contacted once recommendations from CDC are reviewed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- 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
There was an opened unlabeled vial of Moderna in the VFC fridge. There had not been any mentions on the group chat of an open Moderna vial (as when we open each vial we let everyone in the chat know) . I grabbed the open vial along with an unopened vial of Moderna and proceeded to the Covid clinic. There were 7 doses of this vaccine given to patients. As of 9/27 we were off on our counts and now realize that the vial that was used on 9/24 to those 7 patients was an expired vial. The vial had originally been opened on 9/23 by RN. These 7 patients have been located and will be contacted once recommendations from CDC are reviewed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 27.09.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Product storage error
Symptomtext
There was an opened unlabeled vial of Moderna in the fridge. There had not been any mentions of an open Moderna vial . I grabbed the open vial along with an unopened vial of Moderna and proceeded to the Covid clinic. There were 7 doses of this vaccine given to patients. As of 9/27 we were off on our counts and now realize that the vial that was used on 9/24 to those 7 patients was an expired vial. The vial had originally been opened on 9/23 by RN. These 7 patients have been located and will be contacted once recommendations from CDC are reviewed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 27.09.2021
- Impfdatum
- 27.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
There was an opened unlabeled vial of Moderna in the fridge. There had not been any mentions on the group chat of an open Moderna vial (as when we open each vial we let everyone in the chat know) . I grabbed the open vial along with an unopened vial of Moderna and proceeded to the Covid clinic. There were 7 doses of this vaccine given to patients. As of 9/27 we were off on our counts and now realize that the vial that was used on 9/24 to those 7 patients was an expired vial. The vial had originally been opened on 9/23 by RN. These 7 patients have been located and will be contacted once recommendations from agency are reviewed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
There was an opened unlabeled vial of Moderna in the VFC fridge. There had not been any mentions on the group chat of an open Moderna vial (as when we open each vial we let everyone in the chat know) . I grabbed the open vial along with an unopened vial of Moderna and proceeded to the Covid clinic. There were 7 doses of this vaccine given to patients. As of 9/27 we were off on our counts and now realize that the vial that was used on 9/24 to those 7 patients was an expired vial. The vial had originally been opened on 9/23 by RN. These 7 patients have been located and will be contacted once recommendations from CDC are reviewed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
There was an opened unlabeled vial of Moderna in the fridge. There had not been any mentions of an open Moderna vial (as when we open each vial we let everyone know . I grabbed the open vial along with an unopened vial of Moderna and proceeded to the clinic. There were 7 doses of this vaccine given to patients. As of 9/27 we were off on our counts and now realize that the vial that was used on 9/24 to those 7 patients was an expired vial. The vial had originally been opened on 9/23 by an RN. These 7 patients have been located and will be contacted once recommendations from CDC are reviewed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 27.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
There was an opened unlabeled vial of Moderna in the fridge. There had not been any mentions on the group chat of an open Moderna vial (as when we open each vial we let everyone in the chat know) . I grabbed the open vial along with an unopened vial of Moderna and proceeded to the Covid clinic. There were 7 doses of this vaccine given to patients. As of 9/27 we were off on our counts and now realize that the vial that was used on 9/24 to those 7 patients was an expired vial. The vial had originally been opened on 9/23 by RN. These 7 patients have been located and will be contacted once recommendations from CDC are reviewed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- N/A
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 27.09.2021
- Impfdatum
- 24.09.2021
- Beginn
- 24.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
Patients first dose of Covid vaccine was Pfizer. This nurse mistakenly gave a Moderna vaccine. Patient monitored for required amount of time, no adverse effects noted. MD aware of event as well as supervisor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic alcohol abuse
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 24.09.2021
- Impfdatum
- 09.09.2021
- Beginn
- 09.09.2021
- 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 was administered a dose of the Moderna COVID 19 vaccine that was beyond 12 hours post punctured.; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 17-Sep-2021 and was forwarded to Moderna on 17-Sep-2021. This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose of the Moderna COVID 19 vaccine that was beyond 12 hours post punctured.) in a 64-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 045C21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Sep-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Sep-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose of the Moderna COVID 19 vaccine that was beyond 12 hours post punctured.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient was administered a dose of the Moderna COVID 19 vaccine that was beyond 12 hours post punctured.) 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. No concomitant medication was reported. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 23.09.2021
- Impfdatum
- 03.09.2021
- Beginn
- 14.09.2021
- Tage bis Beginn
- 11,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
Severely swollen lymph node in groin area (almost the size of an egg) currently on Day 7
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- ALL Leukemia pH+
- Vorgeschichte
- Bone Marrow recipient (10/2020)
- Andere Medikamente
- Sprycell / Dysatnib 50 mg daily
- Allergien
- Premedications are given when getting blood transfusions
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 23.09.2021
- Impfdatum
- 21.09.2021
- Beginn
- 21.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Dysstasia
Fall
Symptomtext
Onset of weakness approximately 4 hrs post vaccination. Unable to stand. Fell to the floor on 4 different occasion over 2 days time. This required calling EMS and neighbors for assistance. Weakness has continued through today. Ordinarily this individual has no problems standing or walking. To ER today for evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- Individual was at the hospital at the time of report.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HTN
- Andere Medikamente
- BP med (unknown name)
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 18.09.2021
- Impfdatum
- 23.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
13 Year-old administered the Moderna vaccine. No side effects reported by patients mother or patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N?A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 09.09.2021
- Beginn
- 09.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Muscular weakness
Symptomtext
Patient states that shes noticed some numbness and less dexterity in 2 fingers on the arm that got the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 16.09.2021
- Impfdatum
- 09.09.2021
- Beginn
- 11.09.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Symptomtext
left arm turn red a streak down front of her arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- chronic leukemia
- Andere Medikamente
- no
- Allergien
- penicillin, grass, dust, perfumes
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 16.09.2021
- Impfdatum
- 16.09.2021
- Beginn
- 16.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Muscle tightness
Symptomtext
neck tightness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Muscle tightness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- amoxicillin
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 16.09.2021
- Impfdatum
- 16.09.2021
- Beginn
- 16.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Muscle tightness
Symptomtext
neck tightness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Muscle tightness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- amoxicillin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 15.09.2021
- Impfdatum
- 09.09.2021
- Beginn
- 09.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Oral discomfort
Skin burning sensation
Symptomtext
Patient described burning sensation on skin and lips. She reported that it felt like a bad sunburn on her skin and her lips felt very chapped.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oral discomfort
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- MEDROXYPROGESTERONE, METFORMIN, LETROZOLE, SIMETHICONE,
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 14.09.2021
- Impfdatum
- 14.09.2021
- Beginn
- 14.09.2021
- 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
Gave moderna to 17yr old patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 13.09.2021
- Impfdatum
- 09.08.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pharyngeal hypoaesthesia
Symptomtext
I noticed that my esophagus would go numb. It doesn't happen all the time, but when I does, I can't feel anything in my throat from the base of my head down to the top of my chest. I can breath and swallow fine, but, for instance, if I'm drinking something, I feel it enter my mouth and start down my throat, but then it disappears until it hits my chest area. It also always feels like there is a lump in my throat right where you start to swallow. That's been pretty common and it makes me want to cough all the time. Again, I've never had trouble breathing or eating.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pharyngeal hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No illness
- Vorgeschichte
- Diabetes, Allergies.
- Andere Medikamente
- Vitamin C, Fish Oil, Aspirin, Metformin, Vitamin, Glimepiride, Tradjenta, Atorvastatin
- Allergien
- None that I'm aware
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 13.09.2021
- Impfdatum
- 13.09.2021
- Beginn
- 13.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Interchange of vaccine products
No adverse event
Symptomtext
Patient came in for her booster shot as she is immunocompromised. Patient completed her two dose series of the Pfizer Vaccine on dates 02/22/2021 and 03/15/2021. Patient was incorrectly administered the Moderna COVID-19 Vaccine as her 3rd shot. Patient did not report of any adverse side effects and was monitored for 16 minutes after injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/a
- Andere Medikamente
- N/A
- Allergien
- No allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 11.09.2021
- Impfdatum
- 10.09.2021
- Beginn
- 10.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 08.09.2021
- Impfdatum
- 11.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
given to 17 year old - no adverse signs or symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- diclofenec nikki
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 07.09.2021
- Impfdatum
- 12.08.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 22,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
PATIENT UNDER AGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 07.09.2021
- Impfdatum
- 12.08.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 22,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
PATIENT UNDER AGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 07.09.2021
- Impfdatum
- 12.08.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 22,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
PATIENT UNDER AGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 07.09.2021
- Impfdatum
- 04.08.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 30,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
PATIENT UNDER AGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 07.09.2021
- Impfdatum
- 04.08.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 30,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
PATIENT UNDER AGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 07.09.2021
- Impfdatum
- 03.08.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 31,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
PATIENT UNDER AGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 07.09.2021
- Impfdatum
- 03.08.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 31,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
PATIENT UNDER AGE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 07.09.2021
- Impfdatum
- 02.08.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 32,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
PATIENT UNDER AGE
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
- 17,0
- Geschlecht
- M
- Eingang
- 03.09.2021
- Impfdatum
- 03.09.2021
- Beginn
- 03.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Vaccine not approved to be given under the age of 18, patient is only 17 years old and was given this vaccine
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
- 17,0
- Geschlecht
- F
- Eingang
- 30.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
PATIENT AGE WAS 17 YEARS. . MOM HAD MARKED MODERNA ON PAPER AND HAD VERBALLY REQUESTED THAT AND VACCINATOR DID NOT CATCH THAT THE PATIENT WAS ONLY 17. MODERNA VACCINE WAS ADMINISTERED. DISCUSSIONS HAVE TAKEN PLACE WITH MOM MAKING HER AWARE SHE SHOULD NOT HAVE BEEN GIVEN MODERNA. SHE HAS NOT HAD ANY REPORTED SIDE EFFECTS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 30.08.2021
- Impfdatum
- 28.08.2021
- Beginn
- 28.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Inappropriate schedule of product administration
Interchange of vaccine products
No adverse event
Symptomtext
This patient received Pfizer for her 1st and 2nd ( 12/22/2020 and 01/10/2021) , but she received Moderna for her booster shot on 08/28/2021. She requested Moderna as a booster shot while she was looking for her vaccine card. It turned out to be Pfizer that she received but she believed Moderna would work better as a booster since she is MD herself. She did not present any side effects or adverse reactions though.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 13.08.2021
- Impfdatum
- 16.07.2021
- Beginn
- 30.07.2021
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysmenorrhoea
Oligomenorrhoea
Symptomtext
Severe menstrual cramps and delayed period
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysmenorrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 12.08.2021
- Impfdatum
- 12.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
immunization was administered 5 days early (day 23)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 11.08.2021
- Impfdatum
- 30.07.2021
- Beginn
- 07.08.2021
- Tage bis Beginn
- 8,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 11.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
A 17 YEAR OLD CAME TO GET MODERNA VACCINE. PHARMACIST DID NOT REALIZE PATIENT WAS NOT OF AGE FOR MODERNA VACCINE. PATIENT AND HIS FATHER WERE CONTACTED. NO SIDE EFFECTS AS OF NOW HAVE BEEN REPORTED BY PATIENT OR FATHER. PATIENT WOULD LIKE TO STILL RECEIVE 2ND DOSE .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 10.08.2021
- Impfdatum
- 09.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- -
- 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
Patient did not have any adverse symptoms. Provider and associate notified and performed outreach to notify patient/parent.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 05.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- 05.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Administered immunization prior to the recommended administer date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- Tremor, Depression
- Andere Medikamente
- Zoloft
- Allergien
- Latex, Sulfamethoxazole, Trimethoprim
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 10.07.2021
- Impfdatum
- 10.07.2021
- Beginn
- 10.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Pallor
Symptomtext
Paleness, sweating
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hyperhidrosis
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- HIGH BLOOD PRESSURE
- Vorgeschichte
- HIGH BLOOD PRESSURE
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 09.07.2021
- Impfdatum
- 06.07.2021
- Beginn
- 09.07.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Epistaxis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Epistaxis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 08.07.2021
- Impfdatum
- 06.07.2021
- Beginn
- 07.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Symptomtext
Pt had red circle develop on her arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -