- Staat
- -
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 06.02.2023
- Impfdatum
- 23.07.2021
- Beginn
- 02.02.2023
- Tage bis Beginn
- 559,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute respiratory failure
Alanine aminotransferase normal
Anaemia
Anion gap
Aspartate aminotransferase normal
Base excess
Bilirubin urine
Blood albumin normal
Blood alkaline phosphatase normal
Blood bicarbonate normal
Blood bilirubin normal
Blood calcium normal
Blood chloride decreased
Blood creatinine increased
Blood glucose increased
Blood lactic acid normal
Blood magnesium increased
Blood pH normal
Symptomtext
Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on February 02, 2023 15:09 EST Verified By: MD on February 02, 2023 15:09 EST Encounter Info: Hospital, Inpatient, 02/02/23 - * Final Report * History of Present Illness/Subjective This is a 51-year-old female with past medical history of anemia, diabetes, hyperlipidemia, hypertension, Raynaud's disease presents to the ED with complaints of dyspnea for the 2 weeks and fatigue. The patient has also been producing green-colored sputum and feeling feverish. She went to a walk-in clinic yesterday and she was prescribed antibiotics and steroids. She used to be a diabetic before but underwent gastric bypass surgery after which she did not require any medications for diabetes. In the ED her vitals are stable except for saturation which is 87% on room air. She is a smoker but she was never formally diagnosed of COPD. labs are sig for Anemia and DKA.XRAY suggestive of pna. pt will be admitted to the ICU for insulin drip Review of Systems 13 point review of system negative except for whats mentioned in my HPI Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) Temp (CEL) 36.9 (36.9-36.9) Temp (FAHR) 98.4 (98.4-98.4), BP 143/75 (117-148)/(75-94), HR 91 (78-99), RR 16 (12-22), O2Sat 90 (73-90) Patient Weight Current Daily Weight: 57.5 kg 02/02/23 Patient Height Current Height: 165.1 cm 02/02/23 Constitutional: No acute distress, well-nourished Eyes: PERRLA, EOMI, normal conjunctiva, no scleral icterus ENMT: Moist oral mucosa Neck: Supple, non-tender, intact range of motion Respiratory: ronchi Cardiovascular: Regular rate and rhythm Gastrointestinal: Soft, non-tender, non-distended Musculoskeletal: No joint swelling, no deformity, intact ROM Integumentary: Intact, warm, dry no rashes Neurologic: Alert & Oriented x 3, no cognitive impairment, no focal deficits Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan 1. Acute respiratory failure J96.00 -The patient is saturating in the 80s in room air -Acute hypoxic respiratory failure secondary to pneumonia -Broad-spectrum antibiotics -Follow pneumonia work-up -Monitor O2 sat 2. Pneumonia J18.9 -Problem #1 3. DKA (diabetic ketoacidosis) E11.10 -Follow diabetic ketoacidosis protocol -Adequate potassium replacement and fluid choice as per the protocol -Bridged with basal bolus -Likely exacerbated by infection 4. HTN (hypertension) I10 -Resume home meds 5. Raynaud disease I73.00 -Resume home meds 6. Hyperlipidemia E78.5 -Continue statin 7. Hx of gastric bypass Z98.84 - Adequate vitamin supplementation Hypoxia R09.02 -Problem 1 Due to a high probability of clinically significant, life threatening deterioration, the patient required my highest level of preparedness to intervene emergently and I personally spent 70 minutes of critical care time directly and personally managing the patient. This critical care time included obtaining a history, examining the patient, pulse oximetry, ordering and reviewing the studies, arranging urgent treatment with development of a management plan, evaluation of the patient?s response to treatment, frequent reassessment, and discussions with other clinicians. The critical care time was performed to assess and manage the high probability of imminent, life-threatening deterioration that could result in multi-organ failure. It was exclusive of separately billable procedures and treating other patients and teaching time. Please see the MDM section and the rest of this note for further information on patient assessment and treatment. Code Status None Recorded Chronic Problem List ADD (attention deficit disorder) Anemia Anxiety Arthralgia Arthritis Asthma Bilateral carpal tunnel syndrome Blood in stool Chronic headache Chronic pain syndrome Chronic pain syndrome Depression Diarrhea Diplopia DM (diabetes mellitus) Encounter for long-term (current) use of medications Fibromyalgia GERD (gastroesophageal reflux disease) Heartburn History of concussion History of intussusception History of opioid abuse Hyperlipidemia Hypertension IBS (irritable bowel syndrome) Long term use of drug Lumbar radiculopathy Malnutrition Migraine MRSA cellulitis MVA (motor vehicle accident) Obesity Otitis media Peripheral edema Peripheral neuropathy Raynaud disease Restrictive lung disease Rheumatoid arthritis Right elbow pain S/P bariatric surgery Swelling of right elbow Tobacco use Procedure/Surgical History ?Manual reduction of bowel intussusception (06/01/2013) ?Colposcopy (12/13/2011) ?egd (01/25/2011) ?History of bariatric surgery. (12/01/2006) ?TL - Tubal ligation (1998) ?BSO - Bilateral salpingo-oophorectomy ?Cholecystectomy ?L CTR DOS 12/6/17 AJM ?Myringotomy ?Rt CTR DOS 11/15/17 AJM Medications Home Medications (27) Active Accu-Chek Aviva Blood Glucose Meter , as directed Accu-Chek Aviva Blood Glucose Meter (ONCE) Not Applicable, Other, Unscheduled, Check Blood Glucose levels TID Accu-Chek Aviva Plus Test Strips Not Applicable, Other, Unscheduled, check blood sugar TID Accu-Chek Fastclix Lancets Not Applicable, Other, Unscheduled, to check blood sugar TID Adderall XR 30 mg capsule 30 mg = 1 Capsule, Orally, Daily, F90.0name brand only per insurance preference albuterol 2.5 mg/3 mL (0.083%) inhalation solution 2.5 mg = 3 mL, PRN, Neb Inhal, Q6H Aldactone 25 mg oral tablet 25 mg = 1 Tablet, Orally, Daily amLODIPine 2.5 mg oral tablet 2.5 mg = 1 Tablet, Orally, Daily cycloBENZaprine 10 mg oral tablet 10 mg = 1 Tablet, PRN, Orally, TID diclofenac 1% topical gel 4 GM, Topical, 4 Times Daily, Use dosing card to measure dose of gel dicyclomine 10 mg oral capsule 10 mg = 1 Capsule, Orally, 4 Times Daily doxycycline monohydrate 100 mg oral capsule 100 mg = 1 Capsule, Orally, BID DULOXetine 60 mg oral delayed release capsule See Instructions, TAKE ONE CAPSULE TWICE A DAY hydroCHLOROthiazide 25 mg oral tablet 25 mg = 1 Tablet, Orally, Daily Imitrex 50 mg oral tablet 50 mg = 1 Tablet, PRN, Orally, Daily, may repeat dose after 2 hours up to a maximum of 200 mg in 24 hours Inderal LA 60 mg oral capsule, extended release 60 mg = 1 Capsule, Orally, Daily meloxicam 15 mg oral tablet 15 mg = 1 Tablet, Orally, Daily methotrexate 2.5 mg oral tablet 12.5 mg = 5 Tablet, Orally, Weekly Neurontin 300 mg oral capsule 300 mg = 1 Capsule, Orally, TID Phenergan 25 mg oral tablet 25 mg = 1 Tablet, Orally, Q6H predniSONE 50 mg oral tablet 50 mg = 1 Tablet, Orally, Daily ProAir HFA 90 mCg/inh inhalation aerosol 2 Puff, PRN, Inhalation, Q4H Remeron 15 mg oral tablet 15 mg = 1 Tablet, Orally, At Bedtime Suboxone 8 mg-2 mg sublingual film 1 Each, Sublingually, BID sucralfate 1 g oral tablet 1 GM = 1 Tablet, Orally, 4 Times Daily torsemide 5 mg oral tablet 5 mg = 1 Tablet, Orally, BID Wellbutrin SR 150 mg/12 hours oral tablet, sustained release 150 mg = 1 Tablet, Orally, BID Active Scheduled Inpatient Medications Sodium Chloride 0.9% PREMIX + Potassium Chloride PREMIX IV 150 mL/hr Insulin regular PREMIX + Sodium Chloride 0.9% PREMIX IV 5.75 mL/hr [0.1 Units/kg/hr] 0.1 Units/kg/hr One-Time Medications Given 02/01/23 00:00:00 TO 02/02/23 15:09:15 MOXifloxacin, Infusion, 400 mg, IVPB, ONCE, (1 DOSE 02/02/23 13:45:00) PRN Medications (0600 - 0559) from 02/01 - 02/02 glucose, Per Glucose Level , IV Push, Unscheduled, 0 Dose(s) Allergies LamISIL (sore in mouth) Lasix (Rash) Keflex (Unknown) Omnicef (Unknown) Rocephin (Unknown) iodinated radiocontrast dyes (Unknown) iodine (Unknown) sulfa drugs (Unknown) Social History Alcohol Current, Wine, 1-2 times per month Electronic Cigarette/Vaping E-Cigarette Use Never. Exercise Exercise frequency: 3-4 times/week. Home/Environment Married, 1 Child Substance Abuse Denies Tobacco Tobacco Use: 10 or more cigarettes (1/2 pack or more)/day in last 30 days. Family History Alcohol abuse: Father. Arthritis..: Mother. Depression: Father. Diabetes...: Grandmother (P). Lab Results All Labs Last 24 hours (No Micro or Pathology) Hematology: WBC: 7.5 k/cumm (02/02/23 11:23:00) RBC: 3.39 million/cumm Low (02/02/23 11:23:00) Hgb: 10.8 GM/dL Low (02/02/23 11:23:00) Hct: 32.5 % Low (02/02/23 11:23:00) MCV: 96 fL (02/02/23 11:23:00) MCH: 31.9 pg (02/02/23 11:23:00) MCHC: 33.3 GM/dL (02/02/23 11:23:00) RDW: 15.4 % High (02/02/23 11:23:00) Platelet: 397 k/cumm (02/02/23 11:23:00) MPV: 7.9 fL (02/02/23 11:23:00) # WBC Counted in Diff: 100 (02/02/23 11:23:00) Neutrophil: 84 % (02/02/23 11:23:00) Lymphocyte: 16 % (02/02/23 11:23:00) Absolute Neutrophil: 6.3 k/cumm (02/02/23 11:23:00) Abs Lymphocyte: 1.2 k/cumm (02/02/23 11:23:00) RBC Morphology: Normal, (02/02/23 11:23:00) Platelet Estimate: Clump Adequate, (02/02/23 11:23:00) Platelet Morphology: Normal, (02/02/23 11:23:00) Chemistry: Sodium SerPl QN: 123 mmol/L Low (02/02/23 11:23:00) Potassium SerPl QN: 4.6 mmol/L (02/02/23 11:23:00) Chloride SerPl QN: 85 mmol/L Low (02/02/23 11:23:00) Carbon Dioxide SerPl QN: 22 mmol/L (02/02/23 11:23:00) Anion Gap: 16 mmol/L High (02/02/23 11:23:00) BUN SerPl QN: 44 mg/dL High (02/02/23 11:23:00) Creatinine SerPl QN: 1.12 mg/dL (02/02/23 11:23:00) Estimated GFR (CKD-EPI, no race): 60 mL/min/1.73m2 (02/02/23 11:23:00) Estimated CRCL (CG): 54 mL/min Low (02/02/23 11:23:00) Glucose SerPl QN: 713 mg/dL Critical (02/02/23 11:23:00) Calcium Total SerPl QN: 10.4 mg/dL (02/02/23 11:23:00) Phosphorus SerPl QN: 2.3 mg/dL Low (02/02/23 12:19:00) Alkaline Phos SerPl QN: 110 Units/L (02/02/23 11:23:00) ALT SerPl QN: 8 Units/L (02/02/23 11:23:00) AST SerPl QN: 7 Units/L Low (02/02/23 11:23:00) Bilirubin Total SerPl QN: 0.8 mg/dL (02/02/23 11:23:00) Total Protein SerPl QN: 7.6 GM/dL (02/02/23 11:23:00) Albumin SerPl QN: 3.9 GM/dL (02/02/23 11:23:00) Magnesium SerPl QN: 2.6 mg/dL (02/02/23 12:19:00) Troponin-I High Sensitivity: <3 (02/02/23 11:23:00) BNP Pl QN: 101 pg/mL High (02/02/23 11:23:00) Lactate Venous Pl QN: 1.6 mmol/L (02/02/23 11:23:00) Gluc-Strip, POC: 450 mg/dL High (02/02/23 15:05:00) pH Bld Venous QN: 7.38 (02/02/23 11:23:00) PCO2 Bld Venous QN: 36 mmHg Low (02/02/23 11:23:00) PO2 Bld Venous QN: 35 mmHg (02/02/23 11:23:00) Base Excess Bld Venous: -3 mmol/L Low (02/02/23 11:23:00) Bicarb Bld Venous Calc: 21 mmol/L Low (02/02/23 11:23:00) O2 Sat Bld Venous Calc: 66 % (02/02/23 11:23:00) Patient Temperature: 37 DegC (02/02/23 11:23:00) Coagulation: D-Dimer Pl QN: 271 ng/mL DDU (02/02/23 11:23:00) Urine Studies: Color: Yellow (02/02/23 12:42:00) Clarity: Clear (02/02/23 12:42:00) Specific Gravity: <=1.005 (02/02/23 12:42:00) pH: 5.5 (02/02/23 12:42:00) Protein: NEGATIVE (02/02/23 12:42:00) Glucose: >=1000 Abnormal (02/02/23 12:42:00) Ketones: 40 Abnormal (02/02/23 12:42:00) Bilirubin: NEGATIVE (02/02/23 12:42:00) Hgb Ur: NEGATIVE (02/02/23 12:42:00) Nitrite: NEGATIVE (02/02/23 12:42:00) Urobilinogen: NormalUro (02/02/23 12:42:00) Leukocyte Esterase Ur: NEGATIVE (02/02/23 12:42:00) All Other Labs: COVID 19 Specimen Source: Nasopharyngeal (02/02/23 12:09:00) Coronavirus SARS-CoV2 Rapid: Not Detected (02/02/23 12:09:00) Micro - Last 7 days Rapid Influenza Method: PCR - Liat (02/02/23 12:09:00) Rapid Influenza A PCR: Not Detected (02/02/23 12:09:00) Rapid Influenza B PCR: Not Detected (02/02/23 12:09:00) Diagnostics Radiology Results - Last 24 hours Across Visits 02/02/2023 12:50 - XR Chest PA or AP Portable IMPRESSION:1. Bilateral lower lobe infiltrates may be multifocal pneumoniaand/or aspiration. Recommend follow-up radiograph in 6-8 weeks toensure resolution posttreatment.Thank you for consulting our team of subspecialty radiologists at Radiology. Please contact us at with any questions. Signature Line Electronically Signed on 02/02/23 15:09 EST ________________________________________________________ MD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 06.12.2022
- Impfdatum
- 18.04.2022
- Beginn
- 26.10.2022
- Tage bis Beginn
- 191,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cerebral artery occlusion
Cerebrovascular accident
Dysarthria
Hemiparesis
Hypercoagulation
Neurological symptom
SARS-CoV-2 test positive
Symptomtext
Patient with history of diabetes, heart disease, prostate cancer. Patient brought to the ED by EMS on 10/26/22 for evaluation of stroke-like symptoms including slurred speech and left-sided weakness. Patient ultimately admitted from 10/26-11/2 for acute stroke. On admission on 10/26 patient tested positive for COVID-19 by PCR. Per chart review, neurology notes "Acute right MCA stroke with occlusion of the R M1 segment - mechanism is mostly likely cardioembolic and hypercoagulable state from cancer and COVID 10/26". He has been vaccinated with the COVID-19 primary series and two boosters.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 10.10.2022
- Impfdatum
- 19.11.2021
- Beginn
- 09.10.2022
- Tage bis Beginn
- 324,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Patient expired 10/9/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Anemia, DVT, atrial fibrillation, recurrent alveolar hemorrhage 2/2 anticoagulation
- Andere Medikamente
- Unknown
- Allergien
- Zosyn, Cefoxitin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 16.08.2022
- Impfdatum
- 17.09.2021
- Beginn
- 08.07.2022
- Tage bis Beginn
- 294,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
COVID-19 pneumonia
Chest pain
Chronic obstructive pulmonary disease
Dyspnoea
Pneumonia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Patient brought to the ED via EMS on 7/8/22 for shortness of breath and right-sided chest pain. At home, patient experiencing right-sided chest pain and increased shortness of breath. He increased his daily oxygen from 2L to 4L NC. COVID PCR test done in ED was positive. Patient admitted from 7/8 - 7/12 for acute hypoxic respiratory failure with combination of pneumonia and COPD, possible bacterial pneumonia, and COVID-19 pneumonia. Patient vaccinated against COVID-19. This meets criteria for vaccine breakthrough case review.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- R upper lung cancer with partial lobectomy, on chemotherapy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 28.06.2022
- Impfdatum
- 04.01.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 171,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
COVID-19
Death
Endotracheal intubation
Hyperthermia
Inappropriate schedule of product administration
Intensive care
Lactic acidosis
Leukocytosis
Mental status changes
Pyrexia
Respiratory failure
SARS-CoV-2 test positive
Sepsis
Unresponsive to stimuli
Symptomtext
Moderna COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Moderna Vaccines on 6/11/21, 7/12/21 and 1/04/22. Presented to the ED via EMS after being found unresponsive in her home, O2 sat of 80% and placed on O2 by EMS. Intubated in ED, fever 105.8 rectally, cooling was initiated. Leukocytosis, acute kidney injury, lactic acidosis. Admitted for UT, AKI, resp failure, AMS, hyperthermia and severe sepsis. Administered IV fluids and abx, transferred to ICU. Previously elected DNR status. Tx'd with decadron, ampicillin, and cefepime. Expired on 6/24/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 1,0
- Labordaten
- Covid + 6/23/22; This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PAF, complete heart block s/p PPM,HLD, hypothyroidism, seizure disorder, pulmonary sarcoidosis, COPD on home O2, PAH, mitral stenosis s/p tissue valve replacement
- Andere Medikamente
- alprazolam, aspirin, baclofen, buspirone, duloxetine, fluticasone/salmeterol, fluticasone, furosemide, gabapentin, ipratropium/albuterol, levetiracetem, levothyroxine, meclizine, montelukast, multivitamin, nystatin, oxycodone, pravastatin,
- Allergien
- Clindamycin, codeine, sulfa antibiotics, penicillins
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 25.04.2022
- Impfdatum
- 07.09.2021
- Beginn
- 22.04.2022
- Tage bis Beginn
- 227,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Patient expired 4/22/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Cardiac pacemaker in situ, Chronic kidney disease stage 3, Epilepsy, not refractory, Hypothyroidism, Legal blindness, Hypopituitarism due to pituitary tumor, Type 2 diabetes mellitus
- Andere Medikamente
- Unknown
- Allergien
- Dorzolamide Hcl-timolol Mal, Ondansetron, Dorzolamide, Hydrocortisone
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 28.10.2021
- Beginn
- 19.01.2022
- Tage bis Beginn
- 83,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute respiratory failure
Angiopathy
Anticoagulant therapy
Asthenia
Blood calcium increased
Blood parathyroid hormone increased
COVID-19
Cerebral disorder
Chest X-ray abnormal
Cognitive disorder
Computerised tomogram thorax abnormal
Confusional state
Coordination abnormal
Culture urine positive
Cystitis
Decreased appetite
Dehydration
Dysphagia
Symptomtext
PROVIDER PROGRESS NOTE 2/8/2022 ASSESSMENT: This is a 85 y.o. female with PMH of Parkinson's disease with unspecified speech disturbance, lack of coordination, and cognitive dysfunction, hypothyroidism, who was diagnosed with COVID on 1/20/22, presented on 2/2/22 with weakness, fatigue, and decreased appetite. PLAN Genearlized weakness Severe fatigue Multifactorial in setting of COVID (positive 1/20), UTI, hypercalcemia, poor PO intake and what is though to be Parkinson's disease (dx'd about 6 months ago). Lives with her husband who is worried he cannot provide support she needs and that she will have a fall at home, has had falls PTA. These were witnessed and with husband's help pt was able to get off ground with no acute injuries. - PT/OT - mgmt of comorbidities as below -TCU at discharge Acute cystitis - resolved UA c/w UTI in setting of leukocytosis. At admit met sepsis criteria with leukocytosis 20k, acute encephalopathy related to infection. Received rocephin in ED. However UCx returned with mixed flora. Given clinical picture with leukocytosis and confusion, favored cont tx of UTI, so rocephin was continued. Thought that UCx could be poor sample and not indicative of non-infection. Reviewed CXR from admit and difficult to discern if opacities from COVID only vs possible superimposed bacterial PNA. Procal checked for further w/u and elevated >3. Started tx for bacterial PNA coverage (see more below). - completed course of IV rocephin for UTI - add'l abx as below for PNA Acute respiratory failure with hypoxia, Improved Bacterial PNA, unspecified organism, CAP No hypoxia noted at admit. CXR with bilateral pulmonary opacities. Initially findings thought to be solely from recent COVID infxn (convalescent). Started on rocephin at admit d/t UTI concerns, since completed. 2/4 noted to have new hypoxia with O2 sats 85% on room air. Has been intermittently on RA and O2 via NC. Procal 3.58->0.38. Poss aspiration component, added anaerobe coverage 2/6. Was on 1L overnight, RA this AM. - cont IV azithromycin for PNA (Day 5 today, complete today) - cont IV unasyn for anaerobe coverage (2/6-2/11), transition to Augmentin at discharge - completed rocephin for UTI -monitor O2 Recent COVID-19 in convalescent phase Sxs of fatigue for roughly 2 weeks PTA. Had productive cough but now resolved. COVID positive on 1/20/22. O2 sats are stable on room air on admit. CXR with pulmonary opacities likely from prior COVID. No indication for decadron or tocilizumab as pt in convalescent phase. - could consider steroid if respiratory status does not improve w/ abx regimen above however pt is convalescent and has other causes for hypoxia - on IVFs for hypercalcemia and poor PO intake, since resolved - monitor - standard dose lovenox as pt in convalescent phase Hypercalcemia, Resolved Primary hyperparathyroidism Calcium 12.3 at admit. Likely multifactorial due to poor PO intake with dehydration over past week or so, possible excess vitamin A (Vit A supps PTA), dehydration, immobility d/t weakness and hyperparathyroidism. Appears up to date on most cancer screenings for woman of 85 y.o. 2/7: iCa normalized to 1.28->1.13. PTH elevated. 2/4: given 1x dose zoledronic acid - discussed w/ pharmacy. Vit d level wnl (not the etiology for elevated PTH) - D/c IVFs at 75cc/hr w/ NS - check iCa daily - hold PTA coenzyme Q10, Vit D and Vit A supps - at DC will likely need bisphosphonate - endocrinology f/u Parkinson's disease Follows with Doctor through clinic of Neurology. Seen 1/4/22 in clinic. Per neuro notes she has some baseline speech disturbance (unspecified type), lack of coordination, and some cognitive dysfunction related to her Parkinson's disease. At her visit 1/4 neuro increased her carbidopa/levodopa to 2 tables 4 times a day. She has been working w/ SLP, OT and PT. 2/6/2022: Per family request, a psychiatrist who has experience with delirium, Parkinson's diseaes, dementia's, etc., provides some insights. He reports roughly 6 months ago she was ambulating independently with just a cane. However has had drastic changes in her mobility. She was diagnosed with Parkinson's disease and has been following with clinic of Neurology where they have been titrating sinemet. Doctor reports the sinemet has led to no improvements and thinks it may be making some aspects worse as it is titrated higher. He states her symptoms seems more atypical parkinson's to him. She has no resting tremor. He states her biggest issue at time of dx was trouble initiating movements. Such as if she was standing and instructed to walk "it was like her foot was nailed to the ground". He has some suspicion for Lewy Body Dementia. He also notes cognitive decline over the past several months where she has been more forgetful. 6 months ago he states she was A&O x3. CT head w/o acute findings. Noted global parenchymal loss, microvascular disease. Today: Pt's husband brought list of requests from a neurologist, vascular dementia work up, MRI, sinemet dose adjustments. Discussed with pt and husband that these items should be done on an outpatient basis with pt's neurologist in clinic. - cont PTA sinemet - Outpatient Neurology follow up for further dementia work up, sinemet dose adjustment, MRI Acute on chronic encephalopathy, metabolic, Improved/Resolved Per husband report, has mild baseline cognitive deficits in setting of Parkinson's disease. I spoke to doctor as above, and 6 months ago was A&Ox3, aware of time/date and surroundings. This has progressively worsened over the past 6 months. Multifactorial in setting of primary hyperparathyroidism w/ hypercalcemia, UTI, COVID, bacterial PNA. Dx of parkinson's in past 6 months as above. Some improvements noted w/ tx of UTI, calcium however remained confused. Today is A&Ox3. - mgmt as above - melatonin qhs - precuations: maintain sleep-wake cycles, minimize night time interruptions Dysphagia w/u Mild Swallowing Impairment SLP consulted - recommend video swallow. Per SLP diet okay for regular food and thin liquids. Video swallow w/out evidence of aspiration. -SLP following -Diet per SLP: Level 7 Reg, no straws, alert and upright for meals Hypothyroidism - cont PTA levothyroxine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 7,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 85 y.o. female with PMH of Parkinson's disease with unspecified speech disturbance, lack of coordination, and cognitive dysfunction, hypothyroidism
- Andere Medikamente
- -
- Allergien
- APPLE
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 05.03.2021
- Beginn
- 29.01.2022
- Tage bis Beginn
- 330,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute respiratory failure
Asthenia
Bradycardia
COVID-19
COVID-19 pneumonia
Cardiac telemetry abnormal
Cardio-respiratory arrest
Death
Fall
Fatigue
Hypotension
Life support
Resuscitation
SARS-CoV-2 test positive
Symptomtext
Moderna COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Moderna Vaccines on 02/05/21 and 03/05/2021. COVID + on 1/20/22. Presented to ED 1/20/22 with hypotension, generalized weakness, fatigue, and 2 falls within the 10 days previous. Admitted for acute hypoxemic respiratory failure due to Covid PNA. Started on 2L of O2. Treated with rocephin, decadron, remdesivir. On 1/29/21 noted on telemetry to become more bradycardic. Code blue called and ACLS protocol was initiated. Given 3 rounds of epinephrine and CPR without ROSC. Patient expired on 1/29/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 9,0
- Labordaten
- 1/20/22 Covid + :This sample was analyzed using the Roche LIAT SARS assay platform using PCR or equivalent Nucleic Acid Amplification (NAA) technology.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HLD,HTN, diverticulosis
- Andere Medikamente
- amlodipine, vitamin C, atenolol, biotin, Os-cal, Vitamin D3, temovate, co-enzyme Q, estrace, Osteo bi-flex, hydrocortisone,ipratropium, ketoconazole, culturelle, multivitamin, prantoprazole, prevident, simvastatin, solifenacin, triamcinolon
- Allergien
- clarithromycin, aspirin, codeine, nitrofuran analogues
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 14.08.2021
- Beginn
- 26.01.2022
- Tage bis Beginn
- 165,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
COVID-19 pneumonia
Death
Intensive care
Positive airway pressure therapy
Respiratory distress
SARS-CoV-2 test positive
Symptomtext
Moderna COVID Vaccine EUA: COVID-19 case resulting in Hospitalization / Death. Patient received Moderna Vaccines on 07/17/21 and 08/14/2021. COVID + on 1/18/22. Presented to ED on 1/18/22. Admitted with respiratory distress and COVID PNA. Transferred to ICU on 1/19/22 due to worsening oxygenation status and maintained on BiPAP and then Airvo. Code status changed to DNAR. During admission, patient treated with rocephin, azithromycin, zosyn, dexamethasone, and remdesivir. Patient wished to remove Airvo. Placed on comfort care on 1/25/22. Expired on 1/26/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 8,0
- Labordaten
- 1/18/22 Covid + : This sample was analyzed on the Luminex Aries platform using RT-PCR technology.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DM2, Afib on xarelto, CAD, CABG, CHF EF 30-35%, CVA, Smoker mixed HLD, HTN, COPD
- Andere Medikamente
- tylenol, aspirin, atorvastatin, carvedilol, furosemide glipizide, isosorbide dinitrate, potassium chloride, xarelto, trazodone
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 20.12.2021
- Impfdatum
- 28.08.2021
- Beginn
- 13.09.2021
- Tage bis Beginn
- 16,0
- Dosis
- 1
- Route/Site
- SYR / UN
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Death
Pulmonary embolism
Symptomtext
Patient died on 9/13/2021 - Cause of Death Pulmonary Thromboemboli
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 20.10.2021
- Impfdatum
- 09.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Death
Myocardial infarction
Respiratory arrest
Resuscitation
Symptomtext
He received the first dose of the Moderna Covid Vaccine at 3 pm on 8/9/2021 and at 12:03 am on 8/10/2021 he stopped breathing. CPR was started, the ambulance was transported him to the hospital, where at 12:59 am he was pronounced dead.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- None - it was determined by the medical examiner that an autopsy was not needed. No tests were done. Family was not offered the option of requesting testing or autopsy
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Atrial Fibrillation, Hypertension
- Andere Medikamente
- -
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 20.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 6,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Back pain
Blood test
Chest pain
Computerised tomogram
Echocardiogram
Electrocardiogram
Hypopnoea
Myocardial infarction
Pericardial effusion
Symptomtext
08/11/2021, 02:00pm: Chest and back between shoulder blades began; patient thought it was indigestion. 08/11/2021, 05:30pm: Blood Pressure taken at home, 145/81; pulse 88; shallow breathing 08/11/2021, 05:56pm: Blood Pressure taken at home, 161/89; pulse 98; shallow breathing 08/11/2021, 06:08pm: Arrive at Hospital Emergency Room; Blood pressure 163/91; extreme pain; initial diagnosis in emergency room was a heart attack. Pericardial Effusion: Please contact Cardiologist, Dr. for additional detailed clinical/medical information regarding this event and follow-up patient care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocardial infarction
- Hospital-Tage
- 3,0
- Labordaten
- 08/11/2021 - 08/13/2021: EKG, Echocardiogram, CT scan, blood tests and perhaps others. Until final hospital insurance billing, a complete list can not be provided.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Diabetes, Type 2
- Andere Medikamente
- Metformin, 850mg before ea meal; Tasulosina, 0.4mg ea night
- Allergien
- Dilaudid
- Vorherige Impfungen
- Blotchy and itchy left arm for (3) days and VERTIGO, age 68, 07/08/2021, COVID19 (Moderna)
- Staat
- LA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 30.07.2021
- Impfdatum
- 28.07.2021
- Beginn
- 30.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Apallic syndrome
Cardio-respiratory arrest
Death
Pyrexia
Resuscitation
Symptomtext
ON 7/30/21 @ 0329 AM, RESIDENT BEGAN RUNNING FEVER 104.2 DEGREES WITH A RESPIRATORY RATE OF 60 BPM. B/P 54/30. PULSE RATE OF 74 BPM. O2 SAT OF 88% ON O2 @ 4LPM PER TRACHE COLLAR. RESIDENTS BASLINE COGNITIVE STATUS UNCHANGED FROM PERSISTENT VEGETATIVE STATE. DR. WAS CALLED BY NURSE AND ORDERS WERE GIVEN TO SEND TO ER. UPON ARRIVAL, EMS HAD TO START CPR AS RESIDENT CODED DURING PICKUP. RESIDENT WAS PRONOUNCED DEAD AT 0520.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardio-respiratory arrest
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- HYPERTENSION DIABETES MELLITUS HYPERLIPIDEMIA CVA EPILEPSY
- Vorgeschichte
- HYPERTENSION DM HYPERLIPIDEMIA
- Andere Medikamente
- ZINC 50MG EVERY DAY VITAMIN C 500MG TWICE A DAY LIPITOR 40MG DAILY ASPIRIN 81MG DAILY VALPROIC ACID 750MG TWICE DAILY SENOKOT ONE TAB AT BEDTIME MIRALAX POWDER 17GM DAILY KEPPRA 750MG TWICE DAILY LANTUS INSULIN 47 UNITS TWICE DAILY NORVASC
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 29.07.2021
- Impfdatum
- 22.07.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
He passed in his sleep that night.; This spontaneous case was reported by a consumer and describes the occurrence of DEATH (He passed in his sleep that night.) in a 52-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. 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. Death occurred on 22-Jul-2021 The patient died on 22-Jul-2021. The cause of death was not reported. It is unknown if an autopsy was performed. No concomitant medication was given. No treatment information was given. Patient received the 1st dose of the Moderna Covid-19 vaccine. He died in his sleep that night. This a report of dead one day after the first dose of the product in an 52-year-old patient with no comorbidities. Very limited information regarding the event has been provided for inferring causality. Further information is not expected.; Sender's Comments: This a report of dead one day after the first dose of the product in an 52-year-old patient with no comorbidities. Very limited information regarding the event has been provided for inferring causality. Further information is not expected.; Reported Cause(s) of Death: unknown
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 27.11.2023
- Impfdatum
- 13.12.2021
- Beginn
- 21.11.2023
- Tage bis Beginn
- 708,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute kidney injury
Anaemia
Blood creatinine increased
Brain natriuretic peptide increased
COVID-19
Cardiac failure congestive
Chest X-ray abnormal
Chronic obstructive pulmonary disease
Condition aggravated
Diuretic therapy
Dyspnoea
Electrocardiogram normal
Haemoglobin decreased
Hypervolaemia
Oedema peripheral
Percutaneous coronary intervention
Pleural effusion
Positive airway pressure therapy
Symptomtext
Patient is a 74 YO female with a history of HFrEF (EF 35-40%), COPD, CKD stage IV, CAD s/p PCI 8/2023, T2DM, HTN, and HLD who presented to Facility on 11/21/2023 with difficulty in breathing. She reports having one week preceding onset of worsening bilateral lower extremity edema. Her dyspnea came on suddenly shortly before arrival to the ED. On arrival, she was noted to have substantially increased work of breathing, for which she was placed on BiPAP. She was mildly tachypneic but otherwise hemodynamically stable and able to maintain adequate oxygenation on BiPAP. Intake lab work was notable for COVID, which she reports testing positive for on 11/11/2023, anemia of Hgb 8.8 which is near her baseline, Cr 3.1 with baseline Cr of 1.4 in September 2022, elevated transaminases, BNP 3.3K, and troponin 107 with 2-hr downtrend to 101 with EKG that did not reveal ST or T wave ischemic changes consistent with type 2 NSTEMI. CXR showed a small left pleural effusion and suspected mild pulmonary vascular congestion and patient was noted to be volume over-loaded on exam. Her presentation was consistent with COPD exacerbation in setting of recent COVID infection for which she was treated with systemic corticosteroids and scheduled duonebs treatments, treatment with remdesivir and antibiotics were not indicated. Her volume over-loaded state was also consistent with CHF exacerbation for which she was diuresed. She was quickly able to be weaned off of BiPAP down to room air and maintaining adequate oxygenation with resolution of her respiratory distress over the course of this admission. She was otherwise clinically stable and discharged in good condition. She was prescribed prednisone burst to complete treatment for her COPD exacerbation. Initiation of diuretic therapy on discharge was deferred given her AKI, with outpatient CMP ordered and can be addressed further on outpatient PCP follow up if appropriate for patient to initiate diuretic therapy. Discharged to home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory distress
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 02.05.2023
- Impfdatum
- 24.07.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 124,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Diplegia
Dyspnoea
Headache
Laboratory test
Laboratory test normal
Mechanical ventilation
Paralysis
Viral test negative
Symptomtext
Bad headache within 24 hours. lasted 8 weeks. then 8 weeks later, both legs became paralyized, up to my body, arms and lower lip. Could not breath . was on respirator for 60 days. hospitalized from November 25 to May 15th of 2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- 165,0
- Labordaten
- Flash drive includes dozens of pages, including negative for tick bite, several viruses
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- mild reaction to corn and wheat Reaction to tramadol
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 29.10.2021
- Beginn
- 27.01.2022
- Tage bis Beginn
- 90,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Bell's palsy
Facial paralysis
Paralysis
Symptomtext
After receiving the vaccine, I had a slowly developing paralysis on the left half of my face occurring over a 2 to 3 day period. I was unable to close my left eye, and I couldn't talk because my mouth was paralyzed on the left side. My doctor said it was a grade 4 paralysis. It was diagnosed as Bell's palsy. I was prescribed prednisone and an anti-viral medication on the 4th day. The study of improvement occurred over the next 10 days. After 10 days the paralysis had ended with the help of the medications. I don't notice anymore paralysis on my face, and I am functioning back to normal now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- NP Thyroid 60mg 1xday Lisinopril 5mg 1xday
- Allergien
- Penicillin Metals
- Vorherige Impfungen
- DPT Vaccine- I had severe swelling of the arm at injection site. I also experienced muscle atrophy at the injection site. (This
- Staat
- MA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 03.08.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 94,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Blood creatine phosphokinase MB increased
Blood creatine phosphokinase increased
C-reactive protein increased
Cardiac failure
Cardiac imaging procedure abnormal
Chest pain
Dyspnoea exertional
Ejection fraction
Ejection fraction normal
Electrocardiogram abnormal
Left ventricular dilatation
Magnetic resonance imaging heart
Myocarditis
Oedema
Pericardial effusion
Pericardial fibrosis
Pericarditis
Pleural effusion
Symptomtext
Patient received 3 Moderna vaccines on 2/4/21, 3/4/21, and 8/3/21. Patient presented to ED on 11/5/21 with acute on chronic DOE and chest pain (history of DOE and chest pain for 2 years and new diagnosis of HFpEF). Troponin was elevated and ECG was consistent with pericarditis. CMR confirmed myopericarditis. Troponin 369 -> 559, CK 867, CK-MB 17.2, CRP 36 and ESR 42. Patient was appropriately treated with indomethacin and colchicine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- 9,0
- Labordaten
- MRI cardiac finding on 11/9/21: overall findings are most consistent with perimyocarditis. The left ventricular size is mildly dilated. The left ventricular ejection fraction is 59 % by Simpson's method. Global left ventricular function is normal. There are no regional wall motion abnormalities of the left ventricular wall. The left ventricular mass is mildly increased. There is a small area of dense focal transmural late gadolinium enhancement of the mid to apical lateral wall. There is evidence of increased T2 signal in this area, indicating the presence of edema. In the current clinical context, these findings most likely represent myocarditis, although a small myocardial infarction may also account for the observed pattern of LGE. Global native T1-time is normal, measured at 1225 m sec (normal native T1-time is 1200 +/- 80 m sec for 3T). Global extracellular volume fraction is 25% (normal extracellular volume fraction cut-off is 32%). There is also mild thickening of the pericardium (3 mm) with mild circumferential late gadolinium enhancement of the pericardium. There is a small pericardial effusion. There is no evidence of constriction. The right ventricular size is normal. Global right ventricular function is mildly decreased with a right ventricular ejection fraction of 45%. There is no late gadolinium enhancement of the right ventricle. Left atrial size is normal. Right atrial size is normal. Small bilateral pleural effusions.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- ADHD, OCD, BPH, hypogonadism, HTN, OSA on CPAP, psoriasis
- Andere Medikamente
- Adderall, multi-vitamin, testosterone injection
- Allergien
- Hibiclens, lisinopril, CoSentry, Norco
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 06.01.2022
- Impfdatum
- 15.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 6,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Dyspnoea
Echocardiogram
Electrocardiogram
Myocarditis
Troponin increased
Symptomtext
Dx: Myopericarditis Tx: Ibuprofen 800mg 4 weekTaper, Cochicine 6 month taper S/Sx: Dyspnea on exertion, chest pressure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Elevated Troponin x 4 but not rising: 50, 43, 52, 51ng/L Normal Echo Normal EKG
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension NAFLD Colon Polyp Mixed Hyperlipidemia Type 2 Diabetes Obesity Elevated Liver Enzymes Generalized Anxiety
- Andere Medikamente
- isosorbide mononitrate 30mg daily benazepril 20mg daily amlodipine 10mg daily omega-3 fatty acids 1g BID metformin 850mg TID Aspirin 81mg daily insulin glargine-lixisenatide 100u-33mcg insulin 36units SQ daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 22.07.2021
- Beginn
- 31.08.2021
- Tage bis Beginn
- 40,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Cardiac discomfort
Chest discomfort
Chills
Cough
Diarrhoea
Dizziness
Dyspnoea
Fatigue
Hallucination
Headache
Muscle spasms
Myalgia
Nausea
Oropharyngeal pain
Pain
Presyncope
Respiratory tract congestion
Symptomtext
Headache (throbbing/horrendous) Chills Sore throat Cough Shortness of breath Tightness in chest around heart Fatigue Hallucinations Dizziness Feel like I?m going to pass out Muscle & body aches Muscle Spasms Joint Pain Congestion Runny nose Nausea Diarrhea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- 08/31/21 AND 09/07/21 VISITED THE DOCTOR BECAUSE OF ADVERSE REACTIONS TO COVID INJECTIONS.
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- ESCITALOPRAM 0.5mg
- Allergien
- CODIENE SULFA DILAUDID PCN
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 05.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test
Diarrhoea
Electrocardiogram
Influenza like illness
Loss of consciousness
Vomiting
Symptomtext
Vomiting, diarrhea, flu-like symptoms and passed-out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- EKG, blood panel and blood pressure.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- VI
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- 25.10.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 35,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Asthenia
Blood test normal
Dizziness
Electrocardiogram normal
Fatigue
Fine motor skill dysfunction
Incontinence
Syncope
Ultrasound Doppler
Urine analysis
Symptomtext
On 11/29 began feeling lightheaded in the morning, was becoming increasingly dizzy, fainted. When woke up from fainting, could not control bowels, and low motor skills. Taken to ER, had an EKG done in ambulance and hospital, both negative, Doppler done on left left (because of previous knee surgery, checking for blood clot). No medication administered, urine tests and blood tests. Nothing unusual. Still experiencing extreme fatigue and weakness. Planning to do a follow-up with primary care provider and neurologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Recently had left knee surgery, asthma, high blood pressure, acid reflux, high cholesterol, take medications to suppress cancerous cells. Predisposed to diabetes
- Andere Medikamente
- Bares 81, Hydrochlorizide 12.5 in morning, Protonix 40 (for acid reflux), inhaler for asthma (albuterol), Symbicort 80/45., Xyzal (for allergies), Lostatin 15 (high blood pressure), Singulair (allergies), Pepsin 40, Letrozole 2.5, Ajovy (m
- Allergien
- Shellfish (migraine headaches)
- Vorherige Impfungen
- After Flu Shot in 2019, began to suffer asthma symptoms for the first time.
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 09.11.2021
- 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: ja
Blood glucose decreased
Dizziness
Dyskinesia
Immunisation
Interchange of vaccine products
Loss of consciousness
Urinary incontinence
Symptomtext
Patient got 2 Pfizer shots at Kaiser and wanted Moderna as the booster. Patient said that his doctor wanted him had Moderna as booster. He was counseled with all side effects after the shots. While sitting in the observing waiting area, he felt dizzy and passed out briefly. His body muscle was jerking and wet his pants. He gained his consciousness after the pharmacist removed his mask. He was alert and answered all the questions. Ambulance arrived. The paramedics checked his blood pressure and blood glucose. His blood pressure was fine but his blood glucose was so low 35mg/dL. The paramedics injected him with Glucagon and gave him a sugar drink. His blood glucose was back to normal. His wife arrived and took him home. The pharmacist checked on him 4 hours later at home. He said that he was fine and just finished the conversation with his Kaiser nurse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE. According to patient: he is healthy with no medical condition
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- Dizzyness
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cardiac failure
Pulmonary oedema
Symptomtext
10/31 Pulmonary edema and Heart failure
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary oedema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anaphylactic reaction
Asthenopia
Dyspnoea
Oropharyngeal pain
Symptomtext
Patient received 0.5 ml of Moderna in left arm at 18:27. Patient stated she has idiopathic anaphylaxis and took 10 ml of oral Benadryl at 1700 prophylactically. Nurse advised patient to wait for 30 minutes for observation. Patient at 30 minutes stated "my throat is sore a little bit and my eyes feel heavy. It's a little bit harder to breath but I'm ok. I had this reaction with my Xolair shot." Nurse notified pharmacist and administered 75mg Benadryl IM at 1914. Observed patient for 15 minutes. Patient stated symptoms subsided. Blood pressure 124/104, HR 82, Resp 20. Pt stable and was discharged home to partner.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Patient pre-medicated with Benadryl approximately 1 hour before receiving vaccination
- Allergien
- Sulfa, all food/liquid except water, airborne allergy - idiopathic anaphylaxis
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 23.10.2021
- Impfdatum
- 12.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Extra dose administered
Feeling hot
Illness
Malaise
Myalgia
Rash
Syncope
Vaccination complication
Vaccination site pain
Symptomtext
unspecified reaction to the first and second shot/wife had the 3rd Moderna COVID-19 vaccine shot and had a reaction; fainted; increasing weakness/very weak; felt sick; received 3rd shot and is not immunocompromised; muscle pain; arm pain pretty same immediate after vaccination; rash; seems to be very hot; not feeling fine; This spontaneous case was reported by a consumer and describes the occurrence of SYNCOPE (fainted) in a 75-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 12-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Oct-2021, the patient experienced EXTRA DOSE ADMINISTERED (received 3rd shot and is not immunocompromised), MYALGIA (muscle pain) and VACCINATION SITE PAIN (arm pain pretty same immediate after vaccination). On 13-Oct-2021, the patient experienced ILLNESS (felt sick). On 14-Oct-2021, the patient experienced SYNCOPE (fainted) (seriousness criterion medically significant) and ASTHENIA (increasing weakness/very weak). In October 2021, the patient experienced FEELING HOT (seems to be very hot), MALAISE (not feeling fine) and RASH (rash). On an unknown date, the patient experienced VACCINATION COMPLICATION (unspecified reaction to the first and second shot/wife had the 3rd Moderna COVID-19 vaccine shot and had a reaction). On 12-Oct-2021, EXTRA DOSE ADMINISTERED (received 3rd shot and is not immunocompromised) had resolved. At the time of the report, SYNCOPE (fainted), ILLNESS (felt sick), ASTHENIA (increasing weakness/very weak), FEELING HOT (seems to be very hot), MALAISE (not feeling fine), VACCINATION COMPLICATION (unspecified reaction to the first and second shot/wife had the 3rd Moderna COVID-19 vaccine shot and had a reaction), MYALGIA (muscle pain) and RASH (rash) outcome was unknown and VACCINATION SITE PAIN (arm pain pretty same immediate after vaccination) had not resolved. No concomitant medications information was reported. No treatment medications were provided. The patients husband reported that his wife had the 3rd Moderna COVID-19 vaccine shot and had a reaction. She felt sick after the shot, by the following day. She had arm pain pretty immediate, the same day. She had increasing weakness and seemed to be very hot, he did not knew if it was fever or not. Early morning on 14 Oct 2021 at 4am his wife got up to get a drink of ginger ale and in the process of taking that out of the fridge she fainted on the floor and she had been very weak all day. There was no such reaction to the first shots. She had muscle pain pretty soon after and that continued and wa still not feeling fine. He had the same side effects as with the first two shots (which he had in February), the same they all had at the moment. When asked if immunocompromised he said he did not know and they assumed the 3rd dose included people over 65 years old as well. The side effects were so much different than the previous doses. She also had a rash, and had that every time she had a bad cold or something like that. This is an spontaneous case concerning a 75 year-old, female patient with unknown clinical history who experienced the unexpected serious event of SYNCOPE and other non-serious events. The event occurs approximately 3 days after the third dose of a COVID-19 vaccine (we do not have information if the first two doses were Spikevax or not). The rechallenge is unknown as per no information is available at the time of the report. The benefit-risk relationship of Spikevax is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 15-Oct-2021: Follow up document received wherein batch number updated.; Sender's Comments: This is an spontaneous case concerning a 75 year-old, female patient with unknown clinical history who experienced the unexpected serious event of SYNCOPE and other non-serious events. The event occurs approximately 3 days after the third dose of a COVID-19 vaccine (we do not have information if the first two doses were Spikevax or not). The rechallenge is unknown as per no information is available at the time of the report. The benefit-risk relationship of Spikevax is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 23.10.2021
- Impfdatum
- 12.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Feeling hot
Malaise
Myalgia
Off label use
Syncope
Vaccination site pain
Symptomtext
fainted; felt sick; arm pain; received 3rd shot and is not immunocompromised; muscle pain; very weak; seems to be very hot; This spontaneous case was reported by a consumer and describes the occurrence of SYNCOPE (fainted) in an 8-decade-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 12-Oct-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 12-Oct-2021, the patient experienced VACCINATION SITE PAIN (arm pain), OFF LABEL USE (received 3rd shot and is not immunocompromised) and MYALGIA (muscle pain). On 13-Oct-2021, the patient experienced MALAISE (felt sick). On 14-Oct-2021, the patient experienced SYNCOPE (fainted) (seriousness criterion medically significant). In October 2021, the patient experienced ASTHENIA (very weak) and FEELING HOT (seems to be very hot). On 12-Oct-2021, OFF LABEL USE (received 3rd shot and is not immunocompromised) had resolved. At the time of the report, SYNCOPE (fainted), VACCINATION SITE PAIN (arm pain), ASTHENIA (very weak) and FEELING HOT (seems to be very hot) outcome was unknown and MALAISE (felt sick) and MYALGIA (muscle pain) had not resolved. Concomitant medications was not reported. Treatment medications was not reported. The patient was in her seventies.The patient had the 3rd Moderna COVID-19 vaccine shot and had a reaction. The patient felt sick after the shot, by the following day. She had arm pain pretty immediate, the same day. She had increasing weakness and seems to be very hot, she had been very weak all day. There was no such reaction to the first shots. She had muscle pain pretty soon after and that continued and was still not feeling fine. When asked if immunocompromised reporter did not know and assumed the 3rd dose included people over 65 years old as well. The side effects were so much different than the previous doses. Company Comment: This case concerns a female patient in her seventies with no relevant medical history who experienced serious unexpected event of syncope. The events occurred approximately two days after the third dose of Spikevax. Reportedly, the patient felt sick with arm pain immediately after vaccination with increasing weakness and feeling hot. The patient got up to get a drink and fainted on the floor and was very weak all day. The patient also had muscle pain pretty soon after vaccination and that continued and she still feels unwell. Rechallenge was not applicable as the event occurred after the third dose so no rechallenge was done and recurrence was not applicable. The benefit-risk relationship of drug is not affected by this report This case was linked to MOD-2021-354077, MOD-2021-354097, MOD-2021-354098, MOD-2021-353426 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 15-Oct-2021: Follow-up received contains significant information: Batch number of booster dose was updated.; Sender's Comments: This case concerns a female patient in her seventies with no relevant medical history who experienced serious unexpected event of syncope. The events occurred approximately two days after the third dose of Spikevax. Reportedly, the patient felt sick with arm pain immediately after vaccination with increasing weakness and feeling hot. The patient got up to get a drink and fainted on the floor and was very weak all day. The patient also had muscle pain pretty soon after vaccination and that continued and she still feels unwell. Rechallenge was not applicable as the event occurred after the third dose so no rechallenge was done and recurrence was not applicable. The benefit-risk relationship of drug is not affected by this report
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 07.10.2021
- Impfdatum
- 01.08.2021
- Beginn
- 26.09.2021
- Tage bis Beginn
- 56,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Symptomtext
Bell's Palsy on the right side of his face; This spontaneous case was reported by a consumer and describes the occurrence of BELL'S PALSY (Bell's Palsy on the right side of his face) in a 58-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 058E21A and 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 26-Sep-2021, the patient experienced BELL'S PALSY (Bell's Palsy on the right side of his face) (seriousness criterion medically significant). At the time of the report, BELL'S PALSY (Bell's Palsy on the right side of his face) outcome was unknown. Concomitant product use was not provided by the reporter. No treatment information was provided. Wife is calling to report that her 58-year-old husband received the first dose of Moderna COVID-19 vaccine on 01AUG2021 in the Right arm (Lot# 091D21A & Exp. Date: Unknown). He had the second Moderna COVID-19 vaccine on 29AUG2021, in the left arm (Lot# 058E21A & Exp. Date: Unknown ). Wife states that on 26SEP2021, He developed Bell's Palsy on the right side of his face (Not confirmed by HCP). Wife states that they have not informed his doctor yet and have not called VAERS. Company comment: This case concerns a 58 year old male with no relevant medical history who experienced Serious expected event of Bell''s palsy approximately a less than a month after receiving the second dose of Moderna Covid 19 vaccine. Rechallenge was not applicable. The benefit-risk relationship is not affected by this report.; Sender's Comments: This case concerns a 58 year old male with no relevant medical history who experienced Serious expected event of Bell''s palsy approximately a less than a month after receiving the second dose of Moderna Covid 19 vaccine. Rechallenge was not applicable. The benefit-risk relationship is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 18.09.2021
- Impfdatum
- 04.08.2021
- Beginn
- 14.09.2021
- Tage bis Beginn
- 41,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Ear pain
Facial paralysis
Headache
Symptomtext
Symptoms of Bells Palsy. Facial paralysis on the left side of my face. Cannot smile on the side and some slight drooping. Mild pain behind my ear and a headache only in the left temple area. Odd mouth sensations as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- None to report
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 03.09.2021
- Impfdatum
- 05.08.2021
- Beginn
- 05.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anaphylactic reaction
Cardiac stress test
Chest pain
Electrocardiogram
Musculoskeletal stiffness
Pericarditis
Symptomtext
3:30 - stiffness in neck, left side, just below jawline 5:30 - sharp internal pain while on light walk, left/center chest (patient practices intense cardiovascular exercise several times weekly) 8:30pm - urgent care diagnosed with anaphylaxis. Prescribed prednisone and Zyrtec. Neck symptoms decreased, chest pain continues 08/06/2021 4:00pm - Urgent Care #2 - EKG, diagnosed with pericarditis, prescribed ibuprofen and Colchicine Symptoms decreased slowly over the next 48hrs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- EKG - 08/06/21 - Stress test - 08/10/21
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Anosmia
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 31.08.2021
- Impfdatum
- 28.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Contusion
Fall
Feeling of body temperature change
Hyperhidrosis
Illness
Impaired work ability
Peripheral swelling
Pyrexia
Thrombosis
Symptomtext
diagnosed with a blood clot in her leg; got really sick.; was hot and cold; had sweating episodes; had a tumble over a board where she hit her leg and it bruised.; she hit her leg and it bruised.; A week and a half after the fall her leg was swelling.; missed several days from work; Every single joint on her body ached; had a fever; This spontaneous case was reported by an other health care professional and describes the occurrence of THROMBOSIS (diagnosed with a blood clot in her leg) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 28-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced THROMBOSIS (diagnosed with a blood clot in her leg) (seriousness criterion medically significant), ILLNESS (got really sick.), FEELING OF BODY TEMPERATURE CHANGE (was hot and cold), HYPERHIDROSIS (had sweating episodes), FALL (had a tumble over a board where she hit her leg and it bruised.), CONTUSION (she hit her leg and it bruised.), PERIPHERAL SWELLING (A week and a half after the fall her leg was swelling.), IMPAIRED WORK ABILITY (missed several days from work), ARTHRALGIA (Every single joint on her body ached) and PYREXIA (had a fever). At the time of the report, THROMBOSIS (diagnosed with a blood clot in her leg), ILLNESS (got really sick.), FEELING OF BODY TEMPERATURE CHANGE (was hot and cold), HYPERHIDROSIS (had sweating episodes), FALL (had a tumble over a board where she hit her leg and it bruised.), CONTUSION (she hit her leg and it bruised.), PERIPHERAL SWELLING (A week and a half after the fall her leg was swelling.), IMPAIRED WORK ABILITY (missed several days from work), ARTHRALGIA (Every single joint on her body ached) and PYREXIA (had a fever) 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. There was no concomitant medication reported. There was no treatment medication reported. Also reported information included, 25th is the due date for second dose. Company comment: 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. However, more information is required for further assessment.; 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. However, more information is required for further assessment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 17.07.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Chills
Dizziness
Fatigue
Feeling abnormal
Feeling cold
Gait disturbance
Head injury
Headache
Hyperhidrosis
Pyrexia
Syncope
Vaccination site pain
Vertigo
Symptomtext
fainted,After she fainted was on the bathroom floor for 2 hours; sweats,then she was sweating profusely; hit her head on the wall,the fact that she fainted and hit her head was awful; severe dizziness; room was spinning and spinning and spinning; it was horrible,the most horrible experience of her life; could not get up of the floor,that night, she couldn't walk; still feels very weak; was freezing cold; extreme fatigue,not as weak as before but still very tired; fever; chills; headache "like I never had in my life",still has a little headache; left arm where she received the injection was sore, tender,(left arm tender)it still is,can move it but it hurts to move it.; This spontaneous case was reported by a consumer and describes the occurrence of SYNCOPE (fainted, After she fainted was on the bathroom floor for 2 hours) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 049E21A and 091D2-1A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was provided. On 17-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 14-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 14-Aug-2021, the patient experienced VACCINATION SITE PAIN (left arm where she received the injection was sore, tender,(left arm tender)it still is,can move it but it hurts to move it.). On 15-Aug-2021 at 3:00 AM, the patient experienced SYNCOPE (fainted,After she fainted was on the bathroom floor for 2 hours) (seriousness criterion medically significant), HYPERHIDROSIS (sweats,then she was sweating profusely), HEAD INJURY (hit her head on the wall,the fact that she fainted and hit her head was awful), DIZZINESS (severe dizziness), VERTIGO (room was spinning and spinning and spinning), FEELING ABNORMAL (it was horrible,the most horrible experience of her life), GAIT DISTURBANCE (could not get up of the floor,that night, she couldn't walk), ASTHENIA (still feels very weak), FEELING COLD (was freezing cold), FATIGUE (extreme fatigue,not as weak as before but still very tired), PYREXIA (fever), CHILLS (chills) and HEADACHE (headache "like I never had in my life",still has a little headache). At the time of the report, SYNCOPE (fainted,After she fainted was on the bathroom floor for 2 hours), HYPERHIDROSIS (sweats,then she was sweating profusely), HEAD INJURY (hit her head on the wall,the fact that she fainted and hit her head was awful), DIZZINESS (severe dizziness), VERTIGO (room was spinning and spinning and spinning), FEELING ABNORMAL (it was horrible,the most horrible experience of her life), FEELING COLD (was freezing cold), PYREXIA (fever) and CHILLS (chills) outcome was unknown, GAIT DISTURBANCE (could not get up of the floor,that night, she couldn't walk) had resolved and ASTHENIA (still feels very weak), VACCINATION SITE PAIN (left arm where she received the injection was sore, tender,(left arm tender)it still is,can move it but it hurts to move it.), FATIGUE (extreme fatigue,not as weak as before but still very tired) and HEADACHE (headache "like I never had in my life",still has a little headache) had not resolved. Concomitant medication included Singular (unspecified). No treatment was reported. Company comment: 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. This case was linked to MOD-2021-287649 (Patient Link).; 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
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 21.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anion gap
Blood calcium decreased
Blood creatinine normal
Blood culture
Blood glucose increased
Blood lactic acid
Blood sodium decreased
Blood urea increased
Carbon dioxide decreased
Colitis
Computerised tomogram thorax abnormal
Haemoglobin decreased
Hypotension
Intensive care
Legionella test
Lung opacity
Malaise
Mental status changes
Symptomtext
Patient presented to ED with altered mental status, unable to provide much history beyond feeling unwell for the past few days. She was found to have metabolic anion gap acidosis, with no osmolar gap. Patient was found to have pneumonia and pancolitis. She was treated with vancomycin and meropenem in ED and transitioned to levofloxacin and metronidazole as an inpatient. She was started on norepinephrine due to low blood pressure. She is COVID-19 negative and legionella negative. Blood cultures are pending. Patient currently in ICU.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Intensive care
- Hospital-Tage
- -
- Labordaten
- 8/23/21 COVID-19 - negative Lactic acid - 3.5 Creatinine - 0.95; BUN - 25; sodium - 125; glucose - 286; calcium - 6.4; CO2 - 12; Anion gap - 32 CT chest PE - no evidence of PE; bilateral ground glass opacities Hemoglobin - 10.9
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Bipolar 2 disorder, COPD, multiple sclerosis, CKD, alcohol abuse, fibromyalgia, anxiety, hypertension, migraines, hepatic steatosis, history of CVA
- Andere Medikamente
- amlodipine, aspirin, atorvastatin, duloxetine, hydrochlorothiazide, hydroxyzine, Creon, Dulera, multivitamin, pantoprazole, topiramate
- Allergien
- ceftriaxone, sumatriptan, bee venom, peanut butter, adhesive tape, erythromycin, lisinopril, ketorloac
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 23.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Anaphylactic reaction
Aphonia
Dysphonia
Pruritus
Throat tightness
Urticaria
Symptomtext
patient reported itching of arms following vaccination, self administered benadryl, evaluated in ED following encounter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- iv dye, demerol, shellfish, levaquin
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 22.08.2021
- Impfdatum
- 28.07.2021
- Beginn
- 05.08.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Facial paralysis
Hypoaesthesia oral
Paraesthesia oral
Symptomtext
8/5/21 - transient tingling in left tongue, 8/6/21 - complete paralysis of left face. Diagnosed with Bell?s palsy. 8/22/21 - still have not recovered
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Oxycodone sensitivity - vomiting
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 11.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood glucose decreased
Eye movement disorder
Loss of consciousness
Symptomtext
The patient received the vaccine and within 2 minutes of receiving the vaccine he passed out. His eyes rolled in the back of his head and passed out in the chair. The patient was moved to the ground and came to within two minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- EMS checked blood sugar and noted it was low
- Aktuelle Erkrankungen
- Asthma, high blood pressure
- Vorgeschichte
- asthma/ hypertension
- Andere Medikamente
- n/a
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 08.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 07.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bell's palsy
Facial paresis
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Tuberous sclerosis, endometriosis, depression, seasonal allergies
- Andere Medikamente
- Zoloft, prenatal vitamins, sunflower lecithin, nexplinon
- Allergien
- Codeine Bactrim Seasonal allergies
- Vorherige Impfungen
- HPV vaccine, migraine/fever/rash
- Staat
- WI
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 08.08.2021
- Impfdatum
- 07.08.2021
- Beginn
- 07.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 05.08.2021
- 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: nein
Dizziness
Emotional distress
Fall
Head injury
Nervousness
Syncope
Symptomtext
Patient received modern vaccine. Was told to wait for signs for allergic reaction. While he was waiting he became dizzy. He tried to get up thinking he would feel better. He had signs of syncope. Female that was accompanying tried to stop him from falling but could not hold him and fell to ground. I was walking back from isle after helping a customer when I saw him already fallen to ground. Female picked him up and put him on chair. I stayed with him the entire time. He was talking and alert. Intern had already called 911. I put cool compress behind neck. I asked if he felt ok. He said he was ok just nervous .He kept apologizing and seemed more embarrassed. I assured him that it happens to some people and nothing to be sorry about. His pulse was good and was talking to us the entire time. He also drank some water. EMT arrived took vitals which were all fine. They suggested he go get head scan since he hit his head when he fell. He agreed and walked out with EMT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- no
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 04.08.2021
- Impfdatum
- 31.07.2021
- Beginn
- 31.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Syncope
Symptomtext
Within 10-15 minutes patient fainted and woke up with no other issues. Breathing was normal throughout this time period. Some sweating.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none stated or listed on agency
- Vorgeschichte
- none stated or listed on agency
- Andere Medikamente
- none stated or listed on agency
- Allergien
- none stated or listed on agency
- Vorherige Impfungen
- fainting in middle school with MMR vaccine
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 02.08.2021
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Head injury
Loss of consciousness
Symptomtext
PATIENT IMMUNIZATION CONSENT FORM WAS REVIEWED AND CONFIRMED PATIENT IS NOT SICK AND CAN RECEIVED SECOND DOSE OF MODERNA COVID VACCINE. PATIENT DID NOT FEEL DIZZY OR FAINT ON FIRST DOSE OF MODERNA OR ANY PREVIOUS VACCINATION. AFTER GETTING THE VACCINE, PATIENT WAS TOLD TO SIT AND WAIT 15 MINUTES IN THE PHARMACY FOR ANY VACCINE ADVERSE REACTION. PATIENT STARTED TO FEEL DIZZY AND HIS WIFE GOT HIM AN ORANGE JUICE TO DRINK. PATIENT WAS ALSO SITTING IN THE BLOOD PRESSURE MACHINE AT THE TIME. SO AS THE PATIENT DRINKS THE ORANGE JUICE, HE PASSED OUT AND HIT THE BACK OF HIS HEAD ON THE FLOOR. WE IMMEDIATELY CALLED ED, AND PHARMACY EMPLOYEES WERE THERE TO ASSIST AND HELP OUT WITH THE SITUATION. PATIENT WAS THEN BROUGHT TO THE ER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 02.08.2021
- Impfdatum
- 26.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Haemorrhage
Injection site bruising
Injection site indentation
Loss of consciousness
Mass
Musculoskeletal stiffness
Nausea
Nodule
Pain
Pain in extremity
Somnolence
Symptomtext
Knocked out; Lot of blood on the cotton; Bruise; Stiff; Knot in my arm; Lump; Pretty painful; Arm is sore or Really sore; Now I am knocked out and wants to get up; Bruising; Injection site knot/mass; Nauseous; This spontaneous case was reported by a consumer and describes the occurrence of LOSS OF CONSCIOUSNESS (Knocked out) in a 56-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Cancer (cancer almost two years ago (radiation)) and Radiation therapy. Concurrent medical conditions included Trigeminal neuralgia (no medication for it). On 26-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced LOSS OF CONSCIOUSNESS (Knocked out) (seriousness criterion medically significant), HAEMORRHAGE (Lot of blood on the cotton), CONTUSION (Bruise), MUSCULOSKELETAL STIFFNESS (Stiff), NODULE (Knot in my arm), MASS (Lump), PAIN (Pretty painful), PAIN IN EXTREMITY (Arm is sore or Really sore), SOMNOLENCE (Now I am knocked out and wants to get up), INJECTION SITE BRUISING (Bruising), INJECTION SITE INDENTATION (Injection site knot/mass) and NAUSEA (Nauseous). At the time of the report, LOSS OF CONSCIOUSNESS (Knocked out), HAEMORRHAGE (Lot of blood on the cotton), CONTUSION (Bruise), MUSCULOSKELETAL STIFFNESS (Stiff), NODULE (Knot in my arm), MASS (Lump), PAIN (Pretty painful), PAIN IN EXTREMITY (Arm is sore or Really sore), SOMNOLENCE (Now I am knocked out and wants to get up), INJECTION SITE BRUISING (Bruising), INJECTION SITE INDENTATION (Injection site knot/mass) and NAUSEA (Nauseous) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medication included: Vitamins. No treatment medication was reported. Patient had the vaccine first dose on Monday (26Jul2021)and it was not very comfortable. This was pretty painful, she flinched. She could not imagine why and then she stayed in the store and she started getting nauseous. She got a cup of water. Her arm was getting stiff so she went to the grocery (store) and she was trying to keep her arm mobile. She did not want it to lock up on her. She finally took the cotton off and there was a lot of blood on the cotton. Then when she came home she said her arm was sore. There was a lump there so she looked in the mirror and she had a bruise and a knot in her arm. Her cousin (who was a nurse) said she should report that. She went to bed yesterday at 5:30/ 6pm and it was 9:45pm when she woke up she thought it was 3 am in the morning. She was knocked out and she wanted to get up. She was not sure if the vaccine was done properly. It was really sore. She did not feel the same when she had her flu shot last time. Done in right arm. Company Comment: Although the date of onset was not reported. There is evidence of temporal relationship between the reported events and mRNA-1273, based on the vaccine administered date and date of report, hence, causal association cannot be excluded.; Sender's Comments: Although the date of onset was not reported. There is evidence of temporal relationship between the reported events and mRNA-1273, based on the vaccine administered date and date of report, hence, causal association cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Trigeminal neuralgia (no medication for it)
- Vorgeschichte
- Medical History/Concurrent Conditions: Cancer (cancer almost two years ago (radiation)); Radiation therapy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 29.07.2021
- Impfdatum
- 28.07.2021
- Beginn
- 28.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Seizure
Symptomtext
PATIENT HAD 2 SEIZURES IMMEDIATELY AFTER ADMINISTRATION WITHIN 5 MINUTES. PATIENT WAS OFFERED 911/EMERGENCY MEDICAL SERVICES, BUT REFUSED. PHARMACIST STAYED WITH PATIENT FOR APPROXIMATELY 15 MINUTES AND THEY LEFT WITH A FRIEND. ENCOURAGED EMERGENCY MEDICAL SERVICES, UNKNOWN IF PATIENT WENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- KNOWN HISTORY OF SEIZURES
- Andere Medikamente
- N/A
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 28.07.2021
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Blindness
Deafness
Loss of consciousness
Vomiting
Symptomtext
3 hours after vaccination, patient lost vision and hearing. She laid down to wait for it to pass. When standing up to go to bathroom, she felt weak and ended up blacking out in bathroom. Time of loss of consciousness is unknown. When patient came to, she vomited several times. She still feels weak the following day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 26.07.2021
- Impfdatum
- 26.07.2021
- Beginn
- 26.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Feeling hot
Loss of consciousness
Tinnitus
Symptomtext
patient felt faint after 1-2 minutes of receiving the vaccine, hot, ears ringing and passed out, came to within 5-10 seconds, and felt okay after sitting for a few minutes
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 25.07.2021
- Impfdatum
- 23.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
After receiving the vaccine patient was taken to the waiting area where he sat down. a few minutes later the technician reported that he needed help. The patient had fainted but came to by the time we made it out to check on him. He reported that he had not eaten that day at all, and he was provided with water with electrolytes. he reported that he was feeling fine and was released to his own care with instructions to contact medical provider if not feeling better or anything worsens.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none known
- Vorgeschichte
- none known
- Andere Medikamente
- none known
- Allergien
- none known
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 24.07.2021
- Impfdatum
- 23.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Symptomtext
Patient said she fainted approximately 10 to 15 minutes later while sitting on the bench by the pharmacy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- Patient checked off "Yes" on immunization consent form but did not disclose what she was allergic to. She mentioned that she had other vaccinations in the past and was okay with them other than the fainting
- Vorherige Impfungen
- Fainting from previous vaccinations
- Staat
- MD
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 22.07.2021
- Impfdatum
- 22.07.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Hyperhidrosis
Hypotonia
Loss of consciousness
Symptomtext
Patient was sitting in observation area immediately post vaccine and he suddenly lost consciousness and his head slumped back briefly. Within 3 minutes patient regained consciousness and was very sweaty and anxious. Provided patient cod compress and water and blood sugar boosting snack. Paramedics arrived.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 22.07.2021
- Impfdatum
- 22.07.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Loss of consciousness
Syncope
Symptomtext
Patient fainted and loss consciousness 2 minutes after receiving vaccine. 911 called and responded
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- taken by ambulence
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- fainting
- Staat
- NC
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 19.07.2021
- Impfdatum
- 16.07.2021
- Beginn
- 16.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Head injury
Syncope
Symptomtext
fainting and hit head....pt opened eyes within 30 seconds of fainting- no difficulty breathings. called EMS due to patient hitting head
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 18.07.2021
- Impfdatum
- 18.07.2021
- Beginn
- 18.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose
Head injury
Immediate post-injection reaction
Syncope
Symptomtext
Patient had an episode of syncope resulting in him hitting his head immediately following the vaccination. EMS was dispatched and the patient was cleared after being monitored. Patient stated that he has passed out in the past after giving blood. The patient had said no to having any history on this on his vaccination consent form. EMS cleared the patient to go home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Blood pressure, heart rate, pulse ox, and blood glucose. All were reported to be in normal range per EMS
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- none reported
- Andere Medikamente
- none reported
- Allergien
- none reported
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- M
- 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: unbekannt
Erholt: ja
Dizziness
Headache
Hyperhidrosis
Syncope
Vision blurred
Symptomtext
Patient experienced dizziness, fainting, sweatiness, and blurry vision 10 minutes after receiving the vaccine. Pharmacist asked patient to sit down and remove facial covering. Pharmacist took blood pressure, first reading was 104/56. Pharmacist offered patient water to drink and continued to monitor patient's symptoms for 40 minutes. Pharmacist took another blood pressure reading and the results were 129/73. Patient stated he no longer feel dizzy or feel fainting. Patient's father took patient home. Pharmacist called patient 2 hours after he left pharmacy. Patient stated he has severe headache. Pharmacist advised patient to take one Tylenol and eat some snack.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 16.07.2021
- Impfdatum
- 14.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Decreased appetite
Loss of consciousness
Pain
Pyrexia
Symptomtext
I passed out the next evening after running a fever and chills body ache no appetite
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Lisinopril 10mg propranolol extended 60mg
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 24.12.2022
- Impfdatum
- 16.09.2022
- Beginn
- 26.11.2022
- Tage bis Beginn
- 71,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Bronchial hyperreactivity
Bronchitis
COVID-19
Chest X-ray
Condition aggravated
SARS-CoV-2 test positive
Symptomtext
COVID, Paxlovid, COVID rebound, exacerbated asthma and reactive airway infection (bronchitis) followed by more asthma
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- COVID tests, chest x-ray
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- Albuterol, Flovent, Premarin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 11.11.2022
- Impfdatum
- 25.03.2021
- Beginn
- 16.09.2022
- Tage bis Beginn
- 540,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Back pain
Condition aggravated
Symptomtext
09/16/22 presents to ED for "back pain". PMHx of "chronic back pain status post L3, L4 fusion"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 22.09.2022
- Impfdatum
- 06.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood test normal
Cardiac imaging procedure normal
Chest X-ray normal
Chest pain
Electrocardiogram normal
Symptomtext
I started getting chest pains in the left side it felt like two fingers were poking my chest very hard it was very centralized, pharmacist offered me water I declined an ambulance was then called. I was taken to the Medical Center.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Heart ultrasound, x-rays and blood work and EKG, all result's were normal.
- Aktuelle Erkrankungen
- Unknown inflammation in body.
- Vorgeschichte
- Asthma.
- Andere Medikamente
- Prednisolone; Simbrinza; Vitamin D; Vitamin C; Prenatal Vitamin.
- Allergien
- Penicillin.
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 20.09.2022
- Impfdatum
- 02.02.2021
- Beginn
- 05.09.2022
- Tage bis Beginn
- 580,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
SOB AND COUGH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- POSITIVE COVID TEST 02/12/21
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ? Acute blood loss anemia 10/7/2016 ? Anemia 10/7/2016 ? Back pain due to mass pressing against the ribs ? Cancer (HCC) skin ca forehead removed ? Cancer of lung (HCC) 2016 right lower lobe ? Deep vein thrombosis (DVT) (HCC) 2016 L. leg/ after lung surgery ? Essential hypertension 10/7/2016 ? HLD (hyperlipidemia) 10/7/2016 ? HTN (hypertension) ? Hypercholesteremia ? Lung mass ? Pyelonephritis ? Renal disease ? Sleep apnea mild - not using CPAP due to back pain from mass ? Status post partial lobectomy of lung 10/7/2016
- Andere Medikamente
- calcium carbonate/vitamin D3 (CALTRATE-600 PLUS VITAMIN D3 ORAL) Cholecalciferol, Vitamin D3, 50 mcg (2,000 unit) oral tablet lisinopril (PRINIVIL;ZESTRIL) 10 mg oral tablet simvastatin (ZOCOR) 20 mg Oral Tab
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 14.09.2022
- Impfdatum
- 10.12.2021
- Beginn
- 20.01.2022
- Tage bis Beginn
- 41,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dialysis
Dyspnoea
SARS-CoV-2 test positive
Symptomtext
Patient was admitted with some increasing shortness of breath for last 2 days and he was recently tested positive at the dialysis unit, apparently 2 days back was positive for COVID-19 virus. In the ER, the patient was placed on some oxygen; however, he was not in any acute distress. He denied any chest pain, etc. No fevers, chills, etc. . He was initially on oxygen, but did ot require any supplemental oxygen. He has been dialyzed several times and is also getting dialysis today prior to discharge. The patient empirically was started on initial dose was IV dexamethasone 6 mg and then was placed on oral dexamethasone 6 mg daily, also was started on ceftriaxone and also got a 1 g of azithromycin as well. The patient is being switched now to Ceftin 125 mg b.i.d. for 5 days at time of discharge. He has been pretty stable symptomatically and is stable for discharge.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- 10/9/19 ESRD (end stage renal disease) (HCC) Date Unknown Angina pectoris (HCC) Date Unknown Anxiety Date Unknown BPH (benign prostatic hyperplasia) Date Unknown Congestive heart failure (HCC) Date Unknown Diabetes Date Unknown Dialysis patient (HCC) Date Unknown Essential hypertension Date Unknown GERD (gastroesophageal reflux disease) Date Unknown HTN (hypertension) Date Unknown Hyperlipidemia Date Unknown Peripheral vascular disease (HCC) Date Unknown RLS (restless legs syndrome) Date Unknown Sensory disorder
- Andere Medikamente
- aspirin low dose 81 MG chew tablet carvedilol (COREG) 3.125 MG tablet docusate sodium (COLACE) 100 MG capsule glipiZIDE CR (GLUCOTROL XL) 10 MG SR tablets midodrine (PROAMITINE) 10 MG tablet rOPINIRole 3 MG tablet sevelamer HCl (RENAG
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 17.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Diarrhoea
Dyspnoea
Fatigue
Headache
Pain
SARS-CoV-2 test negative
Vomiting
Symptomtext
Severe headache, fatigue and body aches for about 3 weeks. Three days after injection I experienced diarrhea and vomiting for a day. That was followed by loss of taste for a few days and difficulty breathing for 5 or 6 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- covid test administered at clinic 5 days after vaccine. It was negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- high blood pressure
- Andere Medikamente
- pantoprazole, diltiazem. losartan, levothyroxine, trazadone, tylenol, zyrtec, vitamin d, multi-vitamin
- Allergien
- amxicillin, adhesive tape, cat dander, ciprofloxacin, kiwi, lisinopril, mango, sulfa, iodinated contrast media, penicillins
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 14.07.2022
- Impfdatum
- 17.11.2021
- Beginn
- 21.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Diarrhoea
Dyspnoea
Headache
Vomiting
Symptomtext
Patient reports after her third COVID shot, she experienced the following: headaches, diarrhea, vomiting, loss of taste, difficultly breathing. These symptoms last for approximately 2 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- none
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 13.02.2021
- Beginn
- 04.05.2022
- Tage bis Beginn
- 445,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Cough
Dyspnoea
Fatigue
Symptomtext
Admitted to hospital for COVID symptoms: fatigue, cough, SOB
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 29.04.2022
- Impfdatum
- 25.10.2021
- Beginn
- 14.01.2022
- Tage bis Beginn
- 81,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aortic dilatation
Arteriogram coronary abnormal
COVID-19
Chest pain
Dizziness
Heart rate irregular
Postural orthostatic tachycardia syndrome
SARS-CoV-2 test positive
Symptomtext
Tested positive for covid virus in Jan 2022. Since then have been experiencing chest pains, dizziness, POTS syndrome, irregular HR.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- CCTA completed: dilated aortic root
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- EDS, PCOS
- Andere Medikamente
- Qysemia, Prenatals, Vit B6, Vit D, Wellbutrin, Calcium,
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 13.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Heart rate increased
Incorrect dose administered
Palpitations
Tinnitus
Symptomtext
From Day 2 until now (MArch 9-th my Birtday) slight headaches, very loud ringing of the ears. Heart beats faster with some palpitations. Never had this before. NOTE: I feel I did not get the .25% dose, but maybe a 50% or 100% dose for my BOOSTER....
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- nope
- Aktuelle Erkrankungen
- nope
- Vorgeschichte
- nope
- Andere Medikamente
- Lisinopril, Pantaprozle, Finasteride, Fish Oil, D, C,
- Allergien
- nope
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 09.03.2022
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure measurement
Erythema
Hypertension
Illness
Ocular hyperaemia
Symptomtext
Became very sick; Blood pressure went up; Eyes were blood shot; Face was beet red; This spontaneous case was reported by a consumer and describes the occurrence of ILLNESS (Became very sick), HYPERTENSION (Blood pressure went up), OCULAR HYPERAEMIA (Eyes were blood shot) and ERYTHEMA (Face was beet red) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. Concurrent medical conditions included Seasonal allergy, Contrast media allergy (contrast dye) and Drug allergy (Allergic to Advair). On 04-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Nov-2021, the patient experienced ILLNESS (Became very sick) (seriousness criterion medically significant), HYPERTENSION (Blood pressure went up) (seriousness criterion medically significant), OCULAR HYPERAEMIA (Eyes were blood shot) (seriousness criterion medically significant) and ERYTHEMA (Face was beet red) (seriousness criterion medically significant). At the time of the report, ILLNESS (Became very sick), HYPERTENSION (Blood pressure went up), OCULAR HYPERAEMIA (Eyes were blood shot) and ERYTHEMA (Face was beet red) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 04-Nov-2021, Blood pressure measurement: high (High) Blood pressure went up. Reported that Patient not had both Acute and Chronic illnesses at the time of vaccination. Patient had not tested Covid positive. Also reported that Other vaccines given within 1 month prior to Moderna COVID-19 vaccine. Concomitant product use was not provided by the reporter. Treatment information was not provided. Patient had not experienced similar event in the past.Outcome of events was reported as gotten better. Symptoms and status was improved. Patient went to Emergency and said it was a reaction from the vaccine. Company comment: This case concerns a 73-year-old, female patient with no relevant medical history, who experienced the unexpected serious events of Illness, Hypertension, Occular Peraema, and Erythema. The events occurred approximately 1 day after the third dose of mRNA-1273 (Moderna covid-19 vaccine). The benefit-risk relationship of mRNA-1273 (Moderna covid-19 vaccine) is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 04-Mar-2022: Follow up includes no new information.; Sender's Comments: This case concerns a 73-year-old, female patient with no relevant medical history, who experienced the unexpected serious events of Illness, Hypertension, Occular Peraema, and Erythema. The events occurred approximately 1 day after the third dose of mRNA-1273 (Moderna covid-19 vaccine). The benefit-risk relationship of mRNA-1273 (Moderna covid-19 vaccine) is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211104; Test Name: Blood pressure; Result Unstructured Data: Blood pressure went up
- Aktuelle Erkrankungen
- Contrast media allergy (contrast dye); Drug allergy (Allergic to Advair); Seasonal allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 28.07.2021
- Beginn
- 29.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pyrexia
Tremor
Vaccination site erythema
Vaccination site pain
Vaccination site pruritus
Vaccination site swelling
Vaccination site warmth
Symptomtext
It is hot again; She started with itching at injection site; It is red again; It is swollen again; She had body shakes next day after receiving 1st dose; It was really hot; About 24 hours later, her left arm at injection site got swollen.; It was really red; It was really painful; She also had fever; This spontaneous case was reported by a consumer and describes the occurrence of TREMOR (She had body shakes next day after receiving 1st dose), VACCINATION SITE WARMTH (It was really hot), VACCINATION SITE WARMTH (It is hot again), VACCINATION SITE PRURITUS (She started with itching at injection site) and VACCINATION SITE SWELLING (About 24 hours later, her left arm at injection site got swollen.) in a 25-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history information was provided. On 28-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Jul-2021, the patient experienced TREMOR (She had body shakes next day after receiving 1st dose), VACCINATION SITE WARMTH (It was really hot), VACCINATION SITE SWELLING (About 24 hours later, her left arm at injection site got swollen.), VACCINATION SITE ERYTHEMA (It was really red), VACCINATION SITE PAIN (It was really painful) and PYREXIA (She also had fever). On 05-Aug-2021, the patient experienced VACCINATION SITE WARMTH (It is hot again), VACCINATION SITE PRURITUS (She started with itching at injection site), VACCINATION SITE ERYTHEMA (It is red again) and VACCINATION SITE SWELLING (It is swollen again). The patient was treated with IBUPROFEN at an unspecified dose and frequency. On 01-Aug-2021, VACCINATION SITE WARMTH (It was really hot), VACCINATION SITE SWELLING (About 24 hours later, her left arm at injection site got swollen.), VACCINATION SITE ERYTHEMA (It was really red) and VACCINATION SITE PAIN (It was really painful) had resolved. At the time of the report, TREMOR (She had body shakes next day after receiving 1st dose) and PYREXIA (She also had fever) had resolved and VACCINATION SITE WARMTH (It is hot again), VACCINATION SITE PRURITUS (She started with itching at injection site), VACCINATION SITE ERYTHEMA (It is red again) and VACCINATION SITE SWELLING (It is swollen again) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medication included: Birth control
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history information was provided.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 24.07.2021
- Beginn
- 24.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Headache
Nausea
Pyrexia
Tremor
Symptomtext
chills were so bad that she couldn't hold anything because her hands were shaking so bad; chills were so bad that she couldn't hold anything because her hands were shaking so bad; fever of 101.8; bad headache; felt nausea; This spontaneous case was reported by a consumer and describes the occurrence of CHILLS (chills were so bad that she couldn't hold anything because her hands were shaking so bad), TREMOR (chills were so bad that she couldn't hold anything because her hands were shaking so bad), PYREXIA (fever of 101.8), HEADACHE (bad headache) and NAUSEA (felt nausea) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 24-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 24-Jul-2021, the patient experienced CHILLS (chills were so bad that she couldn't hold anything because her hands were shaking so bad), TREMOR (chills were so bad that she couldn't hold anything because her hands were shaking so bad), PYREXIA (fever of 101.8), HEADACHE (bad headache) and NAUSEA (felt nausea). On 26-Jul-2021, CHILLS (chills were so bad that she couldn't hold anything because her hands were shaking so bad), TREMOR (chills were so bad that she couldn't hold anything because her hands were shaking so bad), HEADACHE (bad headache) and NAUSEA (felt nausea) had resolved and PYREXIA (fever of 101.8) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 24-Jul-2021, Pyrexia: 101.8 (High) 101.8. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No relevant concomitant medications were reported. No treatment information was provided. Upon in internal review on 04-Aug-2021, the age was corrected to 69 years
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210724; Test Name: Fever; Result Unstructured Data: 101.8
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 28.06.2021
- Beginn
- 26.07.2021
- Tage bis Beginn
- 28,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amenorrhoea
Antral follicle count
Blood luteinising hormone decreased
Blood oestrogen decreased
Blood prolactin normal
Blood test
Blood thyroid stimulating hormone decreased
Hot flush
Impaired work ability
Magnetic resonance imaging normal
Malaise
Menopause
Menstrual disorder
Palpitations
Pituitary scan
Somatic symptom disorder of pregnancy
Symptomtext
On 6/28/21 I received my 1st dose, the following cycle was 21 days long (my cycle averages 27 days) with a 10 day luteal phase. On 7/26/21 I received my second dose and was very sick and was off work for several days, visit to the ED for heart palpitations and the following cycle was 22 days long with an 8 day luteal phase. The following cycle was 31 days long with a 9 day luteal phase. The following cycle was a chemical pregnancy and I haven't had a period since. It has been 98 days. I track my hormones with the Mira device and noticed that my estrogen started to wind down cycle after cycle since receiving the vaccine and my LH surge has basically been non-existent. My provider attempted to induce a period but nothing happened so bloodwork was done. In the meantime I have been having some pretty severe hot flashes so the hypothesis was that I was in perimenopause since I am 41. My provider was surprised at the results of the bloodwork. My FSH was 1.67, estrogen <5 and my LH 0.21. My AMH is stable and right for my age, prolactin is normal (11.6) and TSH is normal (1.30) and my follicle count is 6 (normal for my age). So I am not in perimenopause but for some reason my body stopped producing estrogen. I had repeat bloodwork done because my provider couldn?t believe I just stopped producing estrogen and the results were the same. I had an MRI of the pituitary gland done to cover all bases; MRI is normal and no issues with pituitary. I am currently on estrogen patches and prometrium to try to restart estrogen production.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- My FSH was 1.67, estrogen <5 and my LH 0.21. My AMH is stable and right for my age, prolactin is normal (11.6) and TSH is normal (1.30) and my follicle count is 6 (normal for my age).
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Bipolar II stable Resolved pre-diabetes with lifestyle modification
- Andere Medikamente
- -
- Allergien
- Doxycyline
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 05.10.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Chills
Dizziness
Echocardiogram abnormal
Headache
Heart rate increased
Mitral valve incompetence
Myalgia
Pain
Palpitations
Pyrexia
Sinus tachycardia
Tricuspid valve incompetence
Ultrasound Doppler
Symptomtext
Severe headache, dizziness, fever, severe body aches, myalgia, elevated heart rate, palpitations, chills, carpet burn feeling to left chest
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Echocardiogram - mitral and tricuspid valve regurgitation 30day Doppler with episodes of sinus tachycardia
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Low vitamin d Constipation
- Andere Medikamente
- Miralax, vitamin d3
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 11.08.2021
- Beginn
- 30.08.2021
- Tage bis Beginn
- 19,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: unbekannt
Erholt: nein
Abdominal X-ray
Abdominal pain
Amylase
Burning sensation
Computerised tomogram abdomen
Dyspnoea
Endoscopy
Full blood count
Lipase
Pain
Pancreatitis
Pulmonary pain
Scan with contrast
Symptomtext
For the first dose of the vaccine on July 14, 2021, after a week I had COVID. For the second dose of the vaccine on August 11, 2021, on August 30, 2021 at about 5am to 6am I had a very strong pain in the abdomen, I felt that I was burning inside and then the pain was so strong that I couldn't breathe anymore because the pain went up to the area of ??the lungs. I was diagnosed with an inflamed pancreas and hospitalized for 5 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 5,0
- Labordaten
- Aug 30, 2021- CBC, CT Abdomen/ Pelvic with Contrast, Amylase and Lipase Labs, XR abdomen September 2, 2021-endoscopy
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- None
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 22.01.2022
- Impfdatum
- 23.10.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate increased
Palpitations
Symptomtext
persistent and random rapid heart palpitations
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- penicilin
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 05.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Herpes ophthalmic
Symptomtext
On the 4th day after my booster I had a flair up of herpetic kerititis in my left eye. Had not had a flair up for approx 18months until this flair up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Evaluated and diagnosed by eye doctor
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Asthma
Condition aggravated
Lung disorder
Malaise
Symptomtext
Within 3 hours of receiving the booster I had all of the symptoms of COVID. Some of the sypmtoms have improved but my lungs are in bad shape. I'm on Prednisone 30mg QD X 10 days, on day 5, some improvement. I have never had this much trouble in my life with asthma. These symptoms started after the 2nd dose of Moderna, got a bit better over the summer, and then escalated with the booster. These symptoms are much worse than any asthma flare up. They continue on and on. I don't know if I will ever be OK again. I regret getting the vaccines and booster. But we were all told they were safe and effective. I don't agree. My asthma was under control previously.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Hypertension; Hypothyroidism; Diabetes
- Andere Medikamente
- Synthroid; Asmanex; Stiolto Respimat; Insulin; Vitamins; Fish Oil
- Allergien
- Octagam; Cephalosporins
- Vorherige Impfungen
- Moderna dose #2
- Staat
- MN
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 29.01.2021
- Beginn
- 09.01.2022
- Tage bis Beginn
- 345,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Cough
Diarrhoea
Dyspnoea
Headache
Oropharyngeal pain
Pain
Pyrexia
Sinus congestion
Symptomtext
sinus congestion headache, body aches, exposure, sore throat, cough, fever, chills, shortness of breath, diarrhea. starting 1/9/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Type II diabetes. Asthma. Arthritis. Depression. Obstructive sleep apnea -- > CPAP. Colonic polyps. Diverticulitis -- > Perf. HTN. Hyperlipidemia. Short term memory loss from MVA 2004. CHF--EF 30% in 2002; EF 50% in 11/2007; 60% in 12/2012; 60% in 6/2013; 55-60% 1/2017; 50-55% (10/2020). Negative Cardiolyte Stress Test 7/2010 and 1/2017. Difficult Intubation for Surgery 8/2013. C Diff 6/2015, recurrence 9/2015. Nephrolithiasis - Lithotripsy 9/2015. Brain Aneurysm 4.5 mm (12/2016) - Neurosurgery - Stable 7/2017 and 7/2018 - Stent placed 9/2019 (see below). LBBB (Noted as old on EKG in 2009). Borderline Aortic Stenosis 1/2019. Controlled Substances Agreement 7/2019. Atrial Flutter--Cardioversion 12/2019 then Ablation 1/2020. Cardiac Sarcoidosis 5/2020 - Not enough to warrant immunosuppressants at this time (10/2020). Nonischemic Cardiomyopathy 5/2020. Cardiac Resynchronization Therapy (CRT) device (CRT-D) Placed 6/2020. Negative Colonoscopy 12/2015 (Hyperplastic Polyps) - Repeat in 5 Years. Has Pacemaker. Negative Coronary Angiogram 11/2021.
- Andere Medikamente
- ?Calcium Citrate-Vitamin D 500-400 MG-UNIT Tablet Chewable 1 tablet Orally Once a day ?Coenzyme Q10 100 MG Capsule 1 tablet Orally before bed ?Albuterol Sulfate ER ?Desoximetasone 0.05 % Cream 1 application Externally two times a
- Allergien
- Penicillin G Codeine Tramadol HCl CEPHALOSPORIN DRUGS: Breathing Difficulty - Allergy
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 01.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Electrocardiogram
Hot flush
Hypertension
Limb discomfort
Pain in extremity
Palpitations
Symptomtext
Due to taking immunosuppressants (Rinvoq), my rheumatologist directed me to halt my meds a week prior to the covid shot and start again 5-7 days after the covid shot. I restarted my medications in that window. 24hrs after my first dose I felt light headed, injection arm (entire arm, not just limited to shoulder) was heavy and hurt, blood pressure high (typically 113/70 but recorded 152/86), hot flashes, felt like heart was pounding. Laying down was only way to feel better, everytime I sat up my blood pressure rose again, even resting was not ideal level. Following day felt better but a couple hours later symptoms started again so I went to urgent care. I did not restart my medication beyond the one dose. Attempted to restart Rinvoq medication again 11 days after shot, again 24hrs later arm was heavy and hurt, blood pressure was up and feeling light headed. Symptoms were not as severe as the first incidence but noticeable enough. Laid in bed to rest. Follow up with general practitioner (same office as Urgent Care) and determined I might be overly sensitive to vaccines and had a hyperactive immune system. I had rashes that also appeared during the month of November that did not abate for several weeks. Restarted Rinvoq 17 days post-shot and finally had no reactions; however, effectiveness of medication has seemingly been diminished and overall health is not the same as prior to 11/1/2021. Discussed events with my rheumatologist who said it sounded like an immunologic reaction but had never heard of such a reaction to the medication with a vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- EKG blood pressure check of swelling in extremities general vitals
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Rheumatoid Arthritis
- Andere Medikamente
- Vitamin D2 50,000IU 1xweekly Rinvoq 1xdaily - halted one week prior to vaccination shot Norethindrone progesterone 1xdaily Azelastine nasal spray 2xdaily
- Allergien
- -
- Vorherige Impfungen
- Similar reaction to shots Day 3 and 21 of Rabies sequence, 37yrs old (11/2020)
- Staat
- IA
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 21.12.2021
- Impfdatum
- 12.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: ja
Asthenia
Chest X-ray normal
Computerised tomogram abdomen normal
SARS-CoV-2 test negative
Tachycardia
Vomiting
White blood cell count increased
Symptomtext
11/15/2021 - patient presented to the emergency department via EMS. Pt states today he was unable to get out his recliner d/t generalized weakness, vomited x2. Mildly tachycardic upon presentation at 110bpm, temperature 99.4F. Patient admitted to hospital for observation and close monitoring for significant weakness. Patient's signs/symptoms were improved the next day - he was able to walk and was discharged home 11/16/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- 1,0
- Labordaten
- 11/15/2021: WBC: 11.20 Chest X-Ray: no evidence of acute cardiopulmonary process CT Abd/Pelvis: No evidence of acute process of abdomen or pelvis SARS-COV-2 PCR: not detected 11/16/2021: WBC: 8.57
- Aktuelle Erkrankungen
- increase in shortness of breath over the past 1 month
- Vorgeschichte
- past medical history: anemia, arthritis, Coronary Artery Disease, Hyperlipidemia, hypertension, Peptic Ulcer Disease, polio
- Andere Medikamente
- -
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 09.10.2021
- Beginn
- 10.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Back pain
Blood test
Bone pain
Burning sensation
Confusional state
Fatigue
Headache
Hyperhidrosis
Hypoaesthesia
Injection site swelling
Magnetic resonance imaging head
Magnetic resonance imaging thoracic
Paraesthesia
Pyrexia
Tremor
Symptomtext
Severe burning in feet sensation Bone pain in lower legs Fever Sweat Injection site swelling to 1/2 baseball size Shakes and tremors Extreme fatigue Lower back pain Confusion Joint pain entire body Severe headache Numbness and tingling left side of face Severe back pain
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- 4,0
- Labordaten
- Blood tests MRI head MRI back Neurologic evaluations Hospital admission
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- HIV High blood pressure
- Andere Medikamente
- Biktarvy Amlodepine Atorvastatin Multi vitamins
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 13.12.2021
- Impfdatum
- 05.10.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 42,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthma
Blood test normal
Bordetella test positive
Chest X-ray normal
Condition aggravated
Symptomtext
I had an asthma attack and there was an unknown trigger for it. I went to Urgent Treatment Center on 11/16/2021. I was prescribed oral prednisone and I had a breathing treatment done when I was at the Emergency Room. On 11/19/2021, I went to the ER again. I received another breathing treatment and oral prednisone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Chest X-ray - negative; Blood work - negative; Pertussis - a positive result
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Hay fever; GERD; Hyperlipidemia; BPHA (enlarged prostate)
- Andere Medikamente
- Crestor 20 mg Protonix 40 mg Proscar 5 mg Breo inhaler 100 mcg Flomax 0.4 mg
- Allergien
- Oxycodone; Levofloxacin; Peanuts, Peanut butter, & Peanut oil; Tomato
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 11.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Fatigue
Headache
Nausea
Neck pain
Pain in extremity
Paraesthesia
Symptomtext
Initial symptoms - left arm pain for 3 days, headache, nausea, fatigue, pain in left arm, back of neck, up back of neck and across shoulder - all within 24 hours. 2nd day tingling in arms, hands, legs and feet. As of 12/11/2021 - I continue to have tingling in left arm, left hand and both legs and feet, fatigue continues and nausea continues. I have no other illnesses and I am not pregnant.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- very mild asthma
- Andere Medikamente
- None
- Allergien
- Sulfa, erythromycin
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 20.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Biopsy skin
Blood test normal
Nerve conduction studies
Nerve injury
Paraesthesia
Pruritus
Symptomtext
About a few days or a week after getting the vaccine I noticed that my face and scalp was itching quite often as well as other body parts . I was just starting to get over a month long period of extreme fatigue and other strange symptoms so maybe this itching was unrelated to the vaccine. The itching and sometimes prickly, pin-prick sensations continued and I consulted a neurologist in early September. A series of blood tests were performed which were all negative. A skin biopsy showed some signs of nerve damage as did an electrical test on my legs. The Doctor put me on Gabapentin for symptom management.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Blood tests (negative). Skin biopsy showed signs of early nerve damage. Electrical test on legs showed mild signs of nerve damage.
- Aktuelle Erkrankungen
- Pelvic floor dysfunction, IBS
- Vorgeschichte
- Pelvic floor dysfunction, IBS
- Andere Medikamente
- Prozac, Atenolol
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 11.11.2021
- Beginn
- 21.11.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Paraesthesia
Pruritus
Urticaria
Symptomtext
10 days later spontaneous urticaria. Random locations. Started legs, groin, base of neck, under arms. Itchy palms, soles of feet. Started topical triamcinolone & Benadryl and oral Allegra. Would still get break thru hives. Went to see Dr 3 days later- prescribed oral methylprednisolone. Had to discontinue after 2 days due to side effects (everything was tingly and lips swelled. Called MD with teledoc who recommended I stop the steroid due to unwanted neuro effect). Now taking 180 mg Allegra BID. If I do only 1 Allegra- will get break through hives after about 12 hours. Awaiting further allergy testing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- H/o partial right lower lobectomy (infancy), h/o gallbladder removal
- Andere Medikamente
- Vitamin D, C, fish oil, biotin, cranberry
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 23.11.2021
- Impfdatum
- 23.08.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 81,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cough
Dizziness
Dyspnoea
Malaise
Pyrexia
Vaccine breakthrough infection
Symptomtext
This case meets criteria for vaccine breakthrough review. Sx include fever, SOB, lightheadedness, malaise, cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- NA
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 9,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Genital herpes
Molluscum contagiosum
Psoriasis
Symptomtext
flared patient's genital herpes, psoriasis & molluscum; caused outbreaks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Psoriasis, mollusum, HSV-2
- Vorgeschichte
- congenital nystagmus, strabismu, CKD III, NSTEMI history, psoriasis, genital herpes, molluscum
- Andere Medikamente
- Lipitor, Zyrtec, vitamin D, Skyrizi, Valtrex
- Allergien
- barbiturate's, benzodiazepines, carbamazepine, cephalosporins, coconut, esomeprazole, bee venom
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 19.11.2021
- Impfdatum
- 11.09.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 37,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Activated partial thromboplastin time
Blister
Blood magnesium
Brain natriuretic peptide
Cardiac failure
Chest X-ray
Condition aggravated
Differential white blood cell count
Electrocardiogram
Fibrin D dimer
Full blood count
Glycosylated haemoglobin
Gout
Metabolic function test
Prothrombin time
Pruritus
SARS-CoV-2 test
Skin exfoliation
Symptomtext
1 week onset of heart failure episode and hospitalization 2 week accelerated gout episode requiring emergency room treatment 1.5 months blistering and peeling of skin requiring over counter anti biotic ointment 1.5 months severe itching arms, legs, and body treated with aloe and cortizone cream
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 3,0
- Labordaten
- on or about 10/18/2021 ekg 12 lead xr chest troponin metabolic panel cbc w/ diff d-dimer aptt protime hemo a1c magnesium bnp sars cov2 basic metabolic cbc troponin cbc w diff basic metabolic
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- heart failure gout
- Andere Medikamente
- lasix alpurinol irbesartin carvidolol
- Allergien
- none
- Vorherige Impfungen
- covid-19 dose #1
- Staat
- IA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 16.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cold sweat
Dizziness
Dyspnoea exertional
Fall
Headache
Photophobia
Tinnitus
Symptomtext
Woke up to a severe headache, ear ringing, light sensitivity Clammy. Lightheaded, fell to the floor. The next morning, continued ear ringing. Lightheadedness and feeling winded with activity.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Anxiety/Depression Biliary Colic
- Andere Medikamente
- Zoloft 200 mg daily
- Allergien
- Caffine Phentermine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 15.11.2021
- Impfdatum
- 12.08.2021
- Beginn
- 09.09.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bacterial infection
Blister
Dyspnoea
Heart rate increased
Hypersensitivity
Pruritus
Urticaria
Symptomtext
Having hives; Itching; Blisters; They got in their pubic area, like an bacterial infection; Shortness of breath; Rapid heart bit; Experienced a allergic reaction that is still going on to these day; Allergic reaction; This spontaneous case was reported by a consumer and describes the occurrence of URTICARIA (Having hives), PRURITUS (Itching), BLISTER (Blisters), BACTERIAL INFECTION (They got in their pubic area, like an bacterial infection) and DYSPNOEA (Shortness of breath) in a 58-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 804f21a and 091d21a) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was provided by the reporter. Concomitant products included CARVEDILOL, APIXABAN (ELIQUIS) and FUROSEMIDE for an unknown indication. On 12-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 09-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 09-Sep-2021, the patient experienced URTICARIA (Having hives), PRURITUS (Itching), BLISTER (Blisters), HYPERSENSITIVITY (Experienced a allergic reaction that is still going on to these day) and HYPERSENSITIVITY (Allergic reaction). 09-Sep-2021, the patient experienced BACTERIAL INFECTION (They got in their pubic area, like an bacterial infection), DYSPNOEA (Shortness of breath) and HEART RATE INCREASED (Rapid heart bit). At the time of the report, URTICARIA (Having hives), PRURITUS (Itching), BLISTER (Blisters), HYPERSENSITIVITY (Experienced a allergic reaction that is still going on to these day) and HYPERSENSITIVITY (Allergic reaction) had not resolved and BACTERIAL INFECTION (They got in their pubic area, like an bacterial infection), DYSPNOEA (Shortness of breath) and HEART RATE INCREASED (Rapid heart bit) outcome was unknown. Treatment included they have been prescribed with two types of antibiotics and nothing has work for an allergic reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- CARVEDILOL; ELIQUIS; FUROSEMIDE.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 14.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 14.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Chest pain
Dyspnoea
Pain
Symptomtext
I awoke around 1200 am last night (11/12) with sharp chest pain that radiated to my back. It was slightly more noticeable on the R side. It made it difficult to breathe. I was able to sleep through the rest of the night and for the most part today a more dull version of the chest pain has been present, at times radiating to my back again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none.
- Vorgeschichte
- none.
- Andere Medikamente
- Fish oil omega 3, vit D, Ashwaganda root.
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 27.10.2021
- Impfdatum
- 26.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest pain
Dyskinesia
Symptomtext
Patient states she woke up at 4am this morning with uncontrolled muscle movements and chest pain. She took a tylenol and xanax, and the symptoms resolved. She has not had any issues since. I instructed her to contact her doctor's office for guidance, and I instructed her to go to the hospital if the symptoms come back before she hears back from her doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 18.10.2021
- Impfdatum
- 14.10.2021
- Beginn
- 14.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Burning sensation
Impaired work ability
Injection site haemorrhage
Malaise
Mobility decreased
Pain
Pain in extremity
Pyrexia
Symptomtext
Patient reported bleeding at injection site at time of vaccine. As evening went on, she began to feel arm pain, felt sick and achy, feverish, and said body felt on fire. Took acetaminophen and iced shoulder. Bump developed on arm where shot was administered. Had arm pain and was hard to lift her arm the following day. She had to leave work and go home to rest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- -
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- 05.10.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Migraine
Symptomtext
Migraine headache; This spontaneous case was reported by a consumer and describes the occurrence of MIGRAINE (Migraine headache) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced MIGRAINE (Migraine headache). At the time of the report, MIGRAINE (Migraine headache) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No Concomitant medication was reported. No treatment Drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 38,0
- 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: nein
Ageusia
Asthenia
Body temperature
Computerised tomogram
Dizziness
Hemiparesis
Hypoaesthesia
Lip swelling
Menstruation irregular
Paraesthesia
Pyrexia
Stress
Swollen tongue
Tongue discomfort
Symptomtext
Numbness on the side of her face; Menstruation came early; Body Is under stress; Dizziness; Tongue has changed; Can't taste; Totally weak/Could not change her linen; Swollen lips; Swollen tongue; Weakness in her right side; needles and pin feeling on the right side of her face/paresthesia right side of face; fever, her body temperature was 99, almost 100; This spontaneous case was reported by a consumer and describes the occurrence of HEMIPARESIS (Weakness in her right side) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. 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 PYREXIA (fever, her body temperature was 99, almost 100). On 02-Oct-2021, the patient experienced HEMIPARESIS (Weakness in her right side) (seriousness criterion medically significant), PARAESTHESIA (needles and pin feeling on the right side of her face/paresthesia right side of face), ASTHENIA (Totally weak/Could not change her linen), LIP SWELLING (Swollen lips) and SWOLLEN TONGUE (Swollen tongue). On an unknown date, the patient experienced HYPOAESTHESIA (Numbness on the side of her face), MENSTRUATION IRREGULAR (Menstruation came early), STRESS (Body Is under stress), DIZZINESS (Dizziness), TONGUE DISCOMFORT (Tongue has changed) and AGEUSIA (Can't taste). At the time of the report, HEMIPARESIS (Weakness in her right side), PARAESTHESIA (needles and pin feeling on the right side of her face/paresthesia right side of face), HYPOAESTHESIA (Numbness on the side of her face), ASTHENIA (Totally weak/Could not change her linen), LIP SWELLING (Swollen lips), SWOLLEN TONGUE (Swollen tongue), MENSTRUATION IRREGULAR (Menstruation came early), STRESS (Body Is under stress), DIZZINESS (Dizziness), TONGUE DISCOMFORT (Tongue has changed), AGEUSIA (Can't taste) and PYREXIA (fever, her body temperature was 99, almost 100) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 01-Oct-2021, Body temperature: 99 (High) her body temperature was 99 almost 100. On 03-Oct-2021, Computerised tomogram: negative (Negative) Negative. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant product use was not provided by reporter. Treatment information was not provided. Company Comment: This case concerns a 38-year-old, female patient with no relevant medical history, who experienced the unexpected event of Hemiparesis. The event occurred approximately 2 days after the first dose of Spikevax. The rechallenge was not applicable, as the event happened after the first dose. The benefit-risk relationship of Spikevax is not affected by this report.; Sender's Comments: This case concerns a 38-year-old, female patient with no relevant medical history, who experienced the unexpected event of Hemiparesis. The event occurred approximately 2 days after the first dose of Spikevax. The rechallenge was not applicable, as the event happened after the first dose. The benefit-risk relationship of Spikevax is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211001; Test Name: Body temperature; Result Unstructured Data: her body temperature was 99 almost 100; Test Date: 20211003; Test Name: stroke test; Test Result: Negative; Result Unstructured Data: Negative.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 08.10.2021
- Impfdatum
- 15.07.2021
- Beginn
- 17.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dyspnoea
Symptomtext
Vaccine administered on 7/15/2021. Symptoms began 2nd day. Woke and couldn't breathe like asthma Continued to use inhalers 8 xs day. Pt thinks he had liquid in lungs. Relieved after 4th day resolved
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None. based on patient experience
- Aktuelle Erkrankungen
- None- 2 days later
- Vorgeschichte
- none
- Andere Medikamente
- NONe
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 08.10.2021
- Impfdatum
- 03.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 29,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Body temperature
Chest pain
Chills
Decreased appetite
Inappropriate schedule of product administration
Nausea
Pain in extremity
Pelvic pain
Pyrexia
Vaccination site bruising
Vaccination site mass
Vaccination site pain
Vaginal haemorrhage
Symptomtext
raised bump at the injection site/The injection site looked like a donut with raised bump in the middle of the bruising; pain in her upper back like someone beat her up; little nauseous; fever of 100.6 degrees F; was tender to the touch day of and the next day; vaginal bleeding/ She was 8 days early/light flow; leg pain; bruising around the injection site/ The injection site looked like a donut with raised bump in the middle of the bruising; appetite was off/appetite was not really there/She had to kind of force herself to eat/She usually had some cravings during her period but did not with this; felt a little bit of chest pain; cramping in her pelvis; second dose on day 54; chills; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE MASS (raised bump at the injection site/The injection site looked like a donut with raised bump in the middle of the bruising), VACCINATION SITE BRUISING (bruising around the injection site/ The injection site looked like a donut with raised bump in the middle of the bruising), DECREASED APPETITE (appetite was off/appetite was not really there/She had to kind of force herself to eat/She usually had some cravings during her period but did not with this), CHEST PAIN (felt a little bit of chest pain) and PELVIC PAIN (cramping in her pelvis) in a 41-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 014F21A and 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 03-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In September 2021, the patient experienced CHILLS (chills). On 25-Sep-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (second dose on day 54). On 26-Sep-2021, the patient experienced VACCINATION SITE BRUISING (bruising around the injection site/ The injection site looked like a donut with raised bump in the middle of the bruising), DECREASED APPETITE (appetite was off/appetite was not really there/She had to kind of force herself to eat/She usually had some cravings during her period but did not with this), CHEST PAIN (felt a little bit of chest pain), PELVIC PAIN (cramping in her pelvis), VAGINAL HAEMORRHAGE (vaginal bleeding/ She was 8 days early/light flow), PAIN IN EXTREMITY (leg pain), VACCINATION SITE PAIN (was tender to the touch day of and the next day) and PYREXIA (fever of 100.6 degrees F). On an unknown date, the patient experienced VACCINATION SITE MASS (raised bump at the injection site/The injection site looked like a donut with raised bump in the middle of the bruising), BACK PAIN (pain in her upper back like someone beat her up) and NAUSEA (little nauseous). The patient was treated with PARACETAMOL (TYLENOL) for Tenderness, at an unspecified dose and frequency. In September 2021, PYREXIA (fever of 100.6 degrees F) had resolved. On 25-Sep-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (second dose on day 54) had resolved. On 27-Sep-2021, CHEST PAIN (felt a little bit of chest pain) outcome was unknown. At the time of the report, VACCINATION SITE MASS (raised bump at the injection site/The injection site looked like a donut with raised bump in the middle of the bruising), VACCINATION SITE BRUISING (bruising around the injection site/ The injection site looked like a donut with raised bump in the middle of the bruising), DECREASED APPETITE (appetite was off/appetite was not really there/She had to kind of force herself to eat/She usually had some cravings during her period but did not with this), PELVIC PAIN (cramping in her pelvis), BACK PAIN (pain in her upper back like someone beat her up), VAGINAL HAEMORRHAGE (vaginal bleeding/ She was 8 days early/light flow), PAIN IN EXTREMITY (leg pain), CHILLS (chills), VACCINATION SITE PAIN (was tender to the touch day of and the next day) and NAUSEA (little nauseous) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 26-Sep-2021, Body temperature: 100.6 degree f (High) 100.6 Degree F. Treatment also included ice and tea. No concomitant medications were reported. This case was linked to MOD-2021-335974 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210926; Test Name: Body temperature; Result Unstructured Data: 100.6 Degree F
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 11.09.2021
- Beginn
- 12.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Hypoaesthesia
Insomnia
Muscular weakness
Neck pain
Paraesthesia
Peripheral swelling
Vaccination site erythema
Vaccination site rash
Symptomtext
Pt called today, 10/06/2021, to report her symptoms that are ongoing. States that the day after receiving her second dose of the Moderna series (09/12/2021) that her whole arm became very swollen, there was a red rash about 2 inches underneath the vaccination site, and she developed a "kink" in her neck. She reports there have been painful tingling sensations down her whole should, arm, and near her breast. Her thumb, index, and middle finger have all become numb, and the tips of her ring finger and pinky are beginning to go numb. She states her left arm is very weak and she cannot use it well. She has only been getting 3 hours of sleep each night since 09/12/2021 due to being so uncomfortable. Pt states all of her symptoms are progressively getting worse. I advised her to go to an urgent care to have a medical evaluation as she has not been evaluated yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None as of this report.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Ibuprofen for pain r/t sore arm
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 06.10.2021
- Impfdatum
- 22.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Epistaxis
Illness
Influenza like illness
Mobility decreased
Pain
Vaccination site reaction
Symptomtext
COVID Arm; Very ill; flu like symptoms; unable to move my arm; pain when moving arm; Today is experiencing a really bad bloody nose on the left nose straw for over 25 minutes now and it is ongoing; This spontaneous case was reported by a consumer and describes the occurrence of EPISTAXIS (Today is experiencing a really bad bloody nose on the left nose straw for over 25 minutes now and it is ongoing), VACCINATION SITE REACTION (COVID Arm), ILLNESS (Very ill), INFLUENZA LIKE ILLNESS (flu like symptoms) and MOBILITY DECREASED (unable to move my arm) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Drug allergy (alergy to codine). On 22-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 23-Sep-2021, the patient experienced EPISTAXIS (Today is experiencing a really bad bloody nose on the left nose straw for over 25 minutes now and it is ongoing). On an unknown date, the patient experienced VACCINATION SITE REACTION (COVID Arm), ILLNESS (Very ill), INFLUENZA LIKE ILLNESS (flu like symptoms), MOBILITY DECREASED (unable to move my arm) and PAIN (pain when moving arm). At the time of the report, EPISTAXIS (Today is experiencing a really bad bloody nose on the left nose straw for over 25 minutes now and it is ongoing) had not resolved, VACCINATION SITE REACTION (COVID Arm) had resolved and ILLNESS (Very ill), INFLUENZA LIKE ILLNESS (flu like symptoms), MOBILITY DECREASED (unable to move my arm) and PAIN (pain when moving arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medication details were not reported by the reporter. Treatment details was not reported by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 28-Sep-2021: Significant follow-up received events and outcome were added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy (alergy to codine)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 04.10.2021
- Impfdatum
- 27.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Palpitations
Sleep disorder
Vomiting
Symptomtext
This spontaneous case reported by a consumer, describes the occurrence of sleep disorder (wakes out of deep sleep), palpitations (pounding heart) and vomiting in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 vaccine, batch/lot# 091D21A) for COVID-19 immunization. The patient's past medical history included a tumor. Concurrent medical conditions included celiac disease. On Jul 27, 2021, patient received the first dose of mRNA-1273 (Moderna COVID-19 vaccine), intramuscular; 1 dosage form. On an unknown date, patient experienced sleep disorder (wakes out of deep sleep), palpitations (pounding heart) and vomiting. At the time of the report, sleep disorder (wakes out of deep sleep), palpitations (pounding heart) and vomiting outcome: unknown. Concomitant medication and treatment information not provided. This case linked to MOD-2021-328145 (patient link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Celiac disease
- Vorgeschichte
- Medical History/Concurrent Conditions: Tumor; celiac disease.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 30.09.2021
- Impfdatum
- 06.08.2021
- Beginn
- 21.09.2021
- Tage bis Beginn
- 46,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Dyspnoea
Inappropriate schedule of product administration
Myalgia
Symptomtext
Shortness of Breath; weird chest feeling; Muscle pain inside the chest; 2nd dose beyond the recommended interval; This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (Shortness of Breath), CHEST DISCOMFORT (weird chest feeling), MYALGIA (Muscle pain inside the chest) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose beyond the recommended interval) in a 22-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 058E21A and 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 21-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 21-Sep-2021, the patient experienced DYSPNOEA (Shortness of Breath), CHEST DISCOMFORT (weird chest feeling) and MYALGIA (Muscle pain inside the chest). 21-Sep-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose beyond the recommended interval). At the time of the report, DYSPNOEA (Shortness of Breath), CHEST DISCOMFORT (weird chest feeling), MYALGIA (Muscle pain inside the chest) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (2nd dose beyond the recommended interval) outcome was unknown. Patient had reported that he was worried about Myocarditis and the pain he was experiencing. Concomitant information was not reported. Treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 30.09.2021
- Impfdatum
- 06.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest discomfort
Chest pain
Headache
Hot flush
Hypoaesthesia
Muscle spasms
Pain in extremity
Product dose omission issue
Symptomtext
did not get her second dose; Lots of headache/I wake up with headaches; I have spasms in my back; Tightness in my chest/Lots of tightness; Numbness in my fingers; Pain in my arms and chest; Pain in my arms and chest; My body felt flushy and hot that lasted 2- 3 days; This spontaneous case was reported by a consumer and describes the occurrence of MUSCLE SPASMS (I have spasms in my back), CHEST DISCOMFORT (Tightness in my chest/Lots of tightness), HYPOAESTHESIA (Numbness in my fingers), PAIN IN EXTREMITY (Pain in my arms and chest) and CHEST PAIN (Pain in my arms and chest) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 06-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Aug-2021, the patient experienced MUSCLE SPASMS (I have spasms in my back), CHEST DISCOMFORT (Tightness in my chest/Lots of tightness), HYPOAESTHESIA (Numbness in my fingers), PAIN IN EXTREMITY (Pain in my arms and chest), CHEST PAIN (Pain in my arms and chest), HOT FLUSH (My body felt flushy and hot that lasted 2- 3 days) and HEADACHE (Lots of headache/I wake up with headaches). On an unknown date, the patient experienced PRODUCT DOSE OMISSION ISSUE (did not get her second dose ). The patient was treated with METOPROLOL for Adverse reaction, at a dose of 1 DF twice a day. At the time of the report, MUSCLE SPASMS (I have spasms in my back), CHEST DISCOMFORT (Tightness in my chest/Lots of tightness), HYPOAESTHESIA (Numbness in my fingers), PAIN IN EXTREMITY (Pain in my arms and chest), CHEST PAIN (Pain in my arms and chest), HOT FLUSH (My body felt flushy and hot that lasted 2- 3 days) and HEADACHE (Lots of headache/I wake up with headaches) had not resolved and PRODUCT DOSE OMISSION ISSUE (did not get her second dose ) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood test: normal (normal) everything seemed fine. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medication of the patient was not reported. The patient did not know if she had fever. The patient had different issues every day and was still experiencing all side effects. The patient did not get her second dose because she was referred to her cardiologist who gave her medicine that did not work. Mother of the patient died with COVID in December and all of her family members tested positive for COVID, only her had not.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Name: blood work; Result Unstructured Data: everything seemed fine
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 24.09.2021
- Impfdatum
- 19.07.2021
- Beginn
- 24.07.2021
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Injection site pain
Pain in extremity
Symptomtext
Had initial pain at injection site however about one week later I experienced Intense aching pain from left side of chest to fingers on left hand. This pain extended through my entire arm for several hours during the first event. This aching returned several times over the following two weeks. Each time extending through my entire arm and into the left side of my chest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Allergic to nuts and fish
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 23.09.2021
- Impfdatum
- 27.07.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 5,0
- Dosis
- UNK
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Blood test
Borrelia test
Chest X-ray
Chills
Computerised tomogram
Cough
Dyspnoea
Full blood count
Headache
Influenza
Legionella test
Pyrexia
Respiratory viral panel
SARS-CoV-2 test
Symptomtext
Persistent Cough Flu - 2 weeks after first dose Persistent chills Fever Persistent headaches Joint aches Occasional episodes of shortness of breath
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 3,0
- Labordaten
- 20+ blood tests while admitted to ER/Hospital Numerous CBC Lymes panel Chest X-ray Chest cat scan Leggionaires blood test Respiratory panel Covid 19 PCR
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure Kidney stones High cholesterol
- Andere Medikamente
- Xarelto 15mg Atorvastatin 10mg Alfuzosin 10mg Telmistartan 12.5 Vitamin C energy boost Collagen
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 18.08.2021
- Beginn
- 18.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Burning sensation
Dizziness
Inflammation
Injection site erythema
Injection site rash
Migraine
Muscular weakness
Pain
Pain in extremity
Paraesthesia
Rash erythematous
SARS-CoV-2 test
Tremor
Symptomtext
I had a sore arm. The next day, I started having tingling, burning feeling in my arm. On the 20th I started having migraines. On 27th, I got a really big rash at the injection site. It was red. I started having pain in my arm and moving up in my back and lower back. I contacted the pharmacy. I googled it and it said that it was "Covid arm". On Monday, I woke up dizzy and lightheaded. The parasitic in my arm. My finger felt like I had a rubber band around it. My legs felt weak and shaky. I felt severe pain in my whole pain. I contact my pain management doctor. I was afraid that I was having a stroke. I was experiencing neurological symptom. On Wednesday I had an appointment. He told me that I was having inflammation. My symptoms are getting worst, and nothing is helping with it. I cannot feel my index finger. I been having pain attack in my arm where I got to the shot was red. They want me to see a disease specialist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- Covid-19 test, blood work.
- Aktuelle Erkrankungen
- Migraine; depression
- Vorgeschichte
- Graves disease; thyroid disease
- Andere Medikamente
- Levothyroxine; Horizons; Otilonium Bromide; Oxycodone
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 17.09.2021
- Impfdatum
- 13.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Dyspnoea
Symptomtext
having trouble breathing; breathing problems are getting worse every day; This spontaneous case was reported by a consumer and describes the occurrence of DYSPNOEA (having trouble breathing) and CONDITION AGGRAVATED (breathing problems are getting worse every day) in a 33-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced DYSPNOEA (having trouble breathing) and CONDITION AGGRAVATED (breathing problems are getting worse every day). At the time of the report, DYSPNOEA (having trouble breathing) and CONDITION AGGRAVATED (breathing problems are getting worse every day) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant medication were not reported by reporter Treatment information was not provided by reporter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 15.09.2021
- Impfdatum
- 21.08.2021
- Beginn
- 29.08.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Computerised tomogram
Dysphagia
Hypoaesthesia
Injection site swelling
Injection site warmth
Migraine
Musculoskeletal discomfort
Musculoskeletal stiffness
Oropharyngeal discomfort
Paraesthesia
Sensation of foreign body
X-ray
Symptomtext
I started with COVID arm on the 8th day after the vaccine. A small raised warm bump at the injection site. I put ice on it and cleared up in a couple days. I then started to have pressure on my neck. On September 1st, I started with a migraine. I also felt like I had something stuck in my throat. Pressure on the right side of my throat. Hard to shallow. I went up to the hospital and waited two hours without being seen. I called the clinic and they said to go back to the hospital. They took x-rays and took blood. They advised everything was clear. They told me to take some Pepcid. They told to see a GI doctor. I can not get into to see them until the 29th. I changed my diet to all liquid. On the 6th I started to lose feeling in my thumb. It spread up to my hand and to my forearm. It went all the way up my body to my left side of my tongue. I went to the ER, and they told me I was having a panic attack. They gave me a CT scan and they did more blood work to check potassium levels. They told me to follow-up with a doctor I am supposed to see them on the 21st of September. I will also get sporadic stiffness in my arm. I have had tingling in my left big toe. I still am unable to eat anything solid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- x-ray Ct scan Blood test
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Migraines
- Andere Medikamente
- -
- Allergien
- EDTA foods Shellfish
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 10.09.2021
- Impfdatum
- 08.09.2021
- Beginn
- 08.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Burning sensation
Electromyogram
Heart rate increased
Hypoaesthesia
Palpitations
Paraesthesia
Pyrexia
Symptomtext
Burning and tingling in hands, as well as Numbness in limbs. Severe fevers for three days and heart palpitation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- Possible Nerve damage as this is side effect described by pharmacist of Moderna on CDC website. Called pharmacist and primary doctor. They prescribed EMG for nerve damage and heart rate is elevated.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Back surgery and nerves. Had surgery years prior on lower back.
- Andere Medikamente
- None
- Allergien
- Cast dye in epidural injection, Moderna Vaccine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 08.09.2021
- Impfdatum
- 06.08.2021
- Beginn
- 08.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Paraesthesia
Symptomtext
Tingling in both feet near the base of my toes and forefoot. Took ibuprofen but does not stop.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Vitamin D
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 08.09.2021
- Impfdatum
- 02.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cardiac flutter
Chest pain
Heart rate
Symptomtext
Heart fluttering; Chest pain; This spontaneous case was reported by a pharmacist and describes the occurrence of CARDIAC FLUTTER (Heart fluttering) in a 40-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 02-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Aug-2021, the patient experienced CARDIAC FLUTTER (Heart fluttering) (seriousness criterion medically significant) and CHEST PAIN (Chest pain). At the time of the report, CARDIAC FLUTTER (Heart fluttering) and CHEST PAIN (Chest pain) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 03-Aug-2021, Heart rate: increased (High) Increased. 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 concomitant medication details was provided. No treatment medication details was provided. Patient did not confirm whether or not she had a history of myocarditis or pericarditis. 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. Further information has been requested.; 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. Further information has been requested.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210803; Test Name: Heart rate; Result Unstructured Data: Increased
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 07.09.2021
- Impfdatum
- 11.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Paraesthesia
Vaccination site pruritus
Vaccination site scar
Vaccination site urticaria
Vaccination site warmth
Symptomtext
Warm to the touch; Tingling; Dollar coin-size welt on my left arm where I received the vaccine; Itching; Small marking on my arm; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE WARMTH (Warm to the touch), PARAESTHESIA (Tingling), VACCINATION SITE PRURITUS (Itching), VACCINATION SITE SCAR (Small marking on my arm) and VACCINATION SITE URTICARIA (Dollar coin-size welt on my left arm where I received the vaccine) in a 40-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 11-Aug-2021, the patient experienced VACCINATION SITE SCAR (Small marking on my arm). On 18-Aug-2021, the patient experienced VACCINATION SITE PRURITUS (Itching). On 19-Aug-2021, the patient experienced VACCINATION SITE WARMTH (Warm to the touch), PARAESTHESIA (Tingling) and VACCINATION SITE URTICARIA (Dollar coin-size welt on my left arm where I received the vaccine). At the time of the report, VACCINATION SITE WARMTH (Warm to the touch), PARAESTHESIA (Tingling), VACCINATION SITE PRURITUS (Itching), VACCINATION SITE SCAR (Small marking on my arm) and VACCINATION SITE URTICARIA (Dollar coin-size welt on my left arm where I received the vaccine) 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 medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 22.07.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 28,0
- Dosis
- 2
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chills
Disorientation
Illness
Pyrexia
Tremor
Vision blurred
Symptomtext
Saturday Morning experienced disorientation like dizziness; real bad vision as well last Saturday Morning; Yesterday patient was still sick on the couch all day until around 6-7o'clock; Fever 103F; Chills; Violently shaking; This spontaneous case was reported by a consumer and describes the occurrence of TREMOR (Violently shaking), DISORIENTATION (Saturday Morning experienced disorientation like dizziness), VISION BLURRED (real bad vision as well last Saturday Morning), ILLNESS (Yesterday patient was still sick on the couch all day until around 6-7o'clock) and PYREXIA (Fever 103F) in a 33-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 091D21A and 078C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included MULTIVITAMIN [VITAMINS NOS], ASCORBIC ACID (VITAMIN C ACID), VITAMIN D NOS and SIMVASTATIN for an unknown indication. On 22-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 19-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 19-Aug-2021, the patient experienced TREMOR (Violently shaking), PYREXIA (Fever 103F) and CHILLS (Chills). On 20-Aug-2021, the patient experienced ILLNESS (Yesterday patient was still sick on the couch all day until around 6-7o'clock). On 21-Aug-2021, the patient experienced DISORIENTATION (Saturday Morning experienced disorientation like dizziness) and VISION BLURRED (real bad vision as well last Saturday Morning). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency. At the time of the report, TREMOR (Violently shaking), DISORIENTATION (Saturday Morning experienced disorientation like dizziness), VISION BLURRED (real bad vision as well last Saturday Morning) and CHILLS (Chills) had not resolved, ILLNESS (Yesterday patient was still sick on the couch all day until around 6-7o'clock) outcome was unknown and PYREXIA (Fever 103F) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 19-Aug-2021, Body temperature: 103 (High) had fever at 103 F all night. Patient was advised to take Tylenol and hydrate. This case was linked to MOD-2021-293388 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210819; Test Name: Body temperature; Result Unstructured Data: had fever at 103 F all night
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- MULTIVITAMIN [VITAMINS NOS]; VITAMIN C ACID; VITAMIN D NOS; SIMVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 20.07.2021
- Beginn
- 20.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal pain upper
Asthenia
Decreased appetite
Dehydration
Diarrhoea
Dizziness
Faeces discoloured
Feeling abnormal
Head discomfort
Headache
Heart rate
Heart rate increased
Mass
Migraine
Nausea
Oropharyngeal pain
Pain
Pyrexia
Symptomtext
Very weak; Diarrhea; Migraine headaches; Dehydrated; Reflux or stomach pain; Covid arm; Light headedness; Dizzy or sleepy; Lost appetite; Throat hurts or irritating; Stool bright red; Pressure on head; Right leg feels like there's lump moving; Pain on left side; Metal feeling in the body; Heart pulsating really fast; Rash on throat; Fever; Nausea; Vomiting; Headache; This spontaneous case was reported by a consumer and describes the occurrence of ASTHENIA (Very weak), DIARRHOEA (Diarrhea), MIGRAINE (Migraine headaches), DEHYDRATION (Dehydrated) and ABDOMINAL PAIN UPPER (Reflux or stomach pain) in a 40-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 088D21A and 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Nickel sensitivity, Latex allergy, Seasonal allergy, Fruit allergy (Allergic to pineapple) and Fruit allergy (Allergic to Banana). Concomitant products included VITAMINS NOS and CALCIUM for an unknown indication. On 20-Jul-2021, the patient received first 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) (Intramuscular) 1 dosage form. On 20-Jul-2021, the patient experienced ASTHENIA (Very weak), DIARRHOEA (Diarrhea), MIGRAINE (Migraine headaches), DEHYDRATION (Dehydrated), ABDOMINAL PAIN UPPER (Reflux or stomach pain), VACCINATION COMPLICATION (Covid arm), DIZZINESS (Light headedness), SOMNOLENCE (Dizzy or sleepy), DECREASED APPETITE (Lost appetite), OROPHARYNGEAL PAIN (Throat hurts or irritating), FAECES DISCOLOURED (Stool bright red), HEAD DISCOMFORT (Pressure on head), MASS (Right leg feels like there's lump moving), PAIN (Pain on left side), FEELING ABNORMAL (Metal feeling in the body), HEART RATE INCREASED (Heart pulsating really fast), RASH (Rash on throat), PYREXIA (Fever), NAUSEA (Nausea), VOMITING (Vomiting) and HEADACHE (Headache). The patient was treated with ONDANSETRON (ZOFRAN [ONDANSETRON]) for Adverse event, at an unspecified dose and frequency and FAMOTIDINE (PEPCID [FAMOTIDINE]) for Adverse event, at an unspecified dose and frequency. At the time of the report, ASTHENIA (Very weak), DIARRHOEA (Diarrhea), MIGRAINE (Migraine headaches), DEHYDRATION (Dehydrated), ABDOMINAL PAIN UPPER (Reflux or stomach pain), VACCINATION COMPLICATION (Covid arm), DIZZINESS (Light headedness), SOMNOLENCE (Dizzy or sleepy), DECREASED APPETITE (Lost appetite), OROPHARYNGEAL PAIN (Throat hurts or irritating), FAECES DISCOLOURED (Stool bright red), HEAD DISCOMFORT (Pressure on head), MASS (Right leg feels like there's lump moving), PAIN (Pain on left side), FEELING ABNORMAL (Metal feeling in the body), HEART RATE INCREASED (Heart pulsating really fast), RASH (Rash on throat), PYREXIA (Fever), NAUSEA (Nausea), VOMITING (Vomiting) and HEADACHE (Headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 20-Jul-2021, Heart rate: high (High) Heart pulsating really fast. Additional information reported include that the patient was feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210720; Test Name: Heart rate; Result Unstructured Data: Heart pulsating really fast
- Aktuelle Erkrankungen
- Fruit allergy (Allergic to pineapple); Fruit allergy (Allergic to Banana); Latex allergy; Nickel sensitivity; Seasonal allergy
- Vorgeschichte
- -
- Andere Medikamente
- VITAMINS NOS; CALCIUM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 10.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Headache
Incorrect route of product administration
Nausea
Pain in extremity
Rash
Tremor
Symptomtext
Dizziness; Leg tremor; Arm pain; Huge rash that comes and goes; Nausea; Headache; Subcutaneous administration; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (Dizziness), TREMOR (Leg tremor), PAIN IN EXTREMITY (Arm pain), RASH (Huge rash that comes and goes) and NAUSEA (Nausea) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 10-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Subcutaneous) 1 dosage form. On 10-Aug-2021, the patient experienced INCORRECT ROUTE OF PRODUCT ADMINISTRATION (Subcutaneous administration). On an unknown date, the patient experienced DIZZINESS (Dizziness), TREMOR (Leg tremor), PAIN IN EXTREMITY (Arm pain), RASH (Huge rash that comes and goes), NAUSEA (Nausea) and HEADACHE (Headache). At the time of the report, DIZZINESS (Dizziness), TREMOR (Leg tremor), PAIN IN EXTREMITY (Arm pain), NAUSEA (Nausea) and HEADACHE (Headache) outcome was unknown, RASH (Huge rash that comes and goes) had not resolved and INCORRECT ROUTE OF PRODUCT ADMINISTRATION (Subcutaneous administration) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Subcutaneous) was unknown. The patient stated that she experienced a huge rash two to three days post-vaccination, which went away then came back. She also experienced nausea, dizziness, headache, tremors in her leg, pain on her arm. The patient stated that her entire arm was in pain the day before the call. No concomitant product use was provided by the reporter. No treatment medications were reported. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 09.08.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Joint swelling
Paraesthesia
Symptomtext
Within minutes ,felt shooting sharp glass like tingling in fingers on right hand that was felt on and off for approximately 30 minutes. Also raised blood pressure . One month later , now swelling in right hand pointer and pinky fingers joints . And continued intermittent raised blood pressure levels.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 02.09.2021
- Impfdatum
- 07.08.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest injury
Erythema
Limb discomfort
Limb injury
Mobility decreased
Swelling
Vaccination site erythema
Symptomtext
Something hit his shoulder,It's a pretty hard hit; there is a little red on the top of his shoulder; there is a little swelling on the top of his shoulder; Turned red around the skin area where he got the vaccine; something hit his chest; His right hand feels very heavy; He could hardly lift it up to his head level; This spontaneous case was reported by a consumer and describes the occurrence of CHEST INJURY (something hit his chest) in a 45-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 07-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Aug-2021, the patient experienced LIMB DISCOMFORT (His right hand feels very heavy) and MOBILITY DECREASED (He could hardly lift it up to his head level). On an unknown date, the patient experienced CHEST INJURY (something hit his chest) (seriousness criterion medically significant), LIMB INJURY (Something hit his shoulder,It's a pretty hard hit), ERYTHEMA (there is a little red on the top of his shoulder), SWELLING (there is a little swelling on the top of his shoulder) and VACCINATION SITE ERYTHEMA (Turned red around the skin area where he got the vaccine). At the time of the report, CHEST INJURY (something hit his chest), LIMB DISCOMFORT (His right hand feels very heavy), MOBILITY DECREASED (He could hardly lift it up to his head level), LIMB INJURY (Something hit his shoulder,It's a pretty hard hit), ERYTHEMA (there is a little red on the top of his shoulder), SWELLING (there is a little swelling on the top of his shoulder) and VACCINATION SITE ERYTHEMA (Turned red around the skin area where he got the vaccine) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No relevant concomitant medications were reported No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 01.09.2021
- Impfdatum
- 04.08.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 13,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Dizziness
Dyspnoea
Pain
Pneumonia
Pyrexia
Respiratory tract congestion
Rhinorrhoea
Symptomtext
Pneumonia - shortness of breath, fluid in lungs, fever, cough, congestion, body aches, dizziness, and runny nose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Listened to lungs via stethescope
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines
- Andere Medikamente
- None
- Allergien
- Sulfa Meds
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 19.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthritis
Gait disturbance
Gait inability
Hypoaesthesia
Muscle spasms
Muscular weakness
Myalgia
Pain
Palpitations
Paraesthesia
Symptomtext
like a cramp; started to limp; arthritis in my knee; pain is horrible; I can't walk; weak legs; muscle pain which started in my right arm; needles began in my body; numbness in my arm; pounding heart; This spontaneous case was reported by a consumer and describes the occurrence of PARAESTHESIA (needles began in my body), HYPOAESTHESIA (numbness in my arm), PALPITATIONS (pounding heart), MUSCLE SPASMS (like a cramp) and GAIT DISTURBANCE (started to limp) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Fibromyalgia. Concomitant products included LOSARTAN and SIMVASTATIN for an unknown indication. On 19-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Aug-2021, 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 experienced PARAESTHESIA (needles began in my body), HYPOAESTHESIA (numbness in my arm), PALPITATIONS (pounding heart), MUSCLE SPASMS (like a cramp), GAIT DISTURBANCE (started to limp), ARTHRITIS (arthritis in my knee), PAIN (pain is horrible), GAIT INABILITY (I can't walk), MUSCULAR WEAKNESS (weak legs) and MYALGIA (muscle pain which started in my right arm). The patient was treated with IBUPROFEN for Pain, at an unspecified dose and frequency and CORTISONE ACETATE (CORTISONE [CORTISONE ACETATE]) at an unspecified dose and frequency. At the time of the report, PARAESTHESIA (needles began in my body), HYPOAESTHESIA (numbness in my arm), PALPITATIONS (pounding heart), MUSCLE SPASMS (like a cramp), GAIT DISTURBANCE (started to limp), ARTHRITIS (arthritis in my knee), PAIN (pain is horrible), GAIT INABILITY (I can't walk), MUSCULAR WEAKNESS (weak legs) and MYALGIA (muscle pain which started in my right arm) outcome was unknown. Test done were ultrasound, X-ray result stated everything was fine First dose given in left non-dominant, Second dose scheduled for 16Aug2021 , numbness spread to my face, and then to my hands and feit was something that bothered me yet, (muscle pain) was in the calf, after three days it was stronger, it then hit me in the back of my knee and thigh, numbness is in my left leg now, I have been walking with a walker CROSSLINK TO SON'S AE MOD21-128924
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Fibromyalgia
- Andere Medikamente
- LOSARTAN; SIMVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- 05.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Head discomfort
Nausea
Tremor
Vaccination site pain
Vaccination site pruritus
Symptomtext
makes my head feel really high; shaking; kinda feel weak; makes my stomach nauseous; shot site was itchy and a little painful; shot site is itchy, was a little painful; This spontaneous case was reported by a consumer and describes the occurrence of HEAD DISCOMFORT (makes my head feel really high), TREMOR (shaking), ASTHENIA (kinda feel weak), VACCINATION SITE PRURITUS (shot site is itchy, was a little painful) and NAUSEA (makes my stomach nauseous) in a 60-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Allergy to antibiotic (Erythromycin) and Drug allergy (Halidol.). Concomitant products included AMITRIPTYLINE, CITALOPRAM, FOLIC ACID, ADALIMUMAB (HUMIRA), HYDROXYCHLOROQUINE, CALCIUM FOLINATE (LEUCOVORINE), LEVOTHYROXINE, LOSARTAN and METHOTREXATE for an unknown indication. On 05-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 05-Aug-2021, the patient experienced VACCINATION SITE PRURITUS (shot site is itchy, was a little painful) and VACCINATION SITE PAIN (shot site was itchy and a little painful). On 09-Aug-2021, the patient experienced HEAD DISCOMFORT (makes my head feel really high), TREMOR (shaking), ASTHENIA (kinda feel weak) and NAUSEA (makes my stomach nauseous). At the time of the report, HEAD DISCOMFORT (makes my head feel really high), TREMOR (shaking), ASTHENIA (kinda feel weak), VACCINATION SITE PRURITUS (shot site is itchy, was a little painful), NAUSEA (makes my stomach nauseous) and VACCINATION SITE PAIN (shot site was itchy and a little painful) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Reported that the patient was having the same as the effects when she took Erythromycin. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to antibiotic (Erythromycin); Drug allergy (Halidol.)
- Vorgeschichte
- -
- Andere Medikamente
- AMITRIPTYLINE; CITALOPRAM; FOLIC ACID; HUMIRA; HYDROXYCHLOROQUINE; LEUCOVORINE; LEVOTHYROXINE; LOSARTAN; METHOTREXATE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 26.08.2021
- Impfdatum
- 19.08.2021
- Beginn
- 20.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood magnesium
Brain natriuretic peptide
Chest pain
Chills
Dizziness
Electrocardiogram
Full blood count
Headache
Hyperhidrosis
Metabolic function test
Symptomtext
dizzy, chills, headache, sweating, severe pain in chest, went to hospital by ambulance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- BNP(NT-PRO) 8/20/2021 CBC with Auto Diff 8/20/2021 Comprehensive metabolic panel8/20/2021 ECG 12 lead 8/20/2021 Magnesium 8/20/2021
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- no prescriptions. fish oil, vit D, Vit C, Multi vit
- Allergien
- latex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 23.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Obsessive-compulsive disorder
Sensitive skin
Symptomtext
ocd worsened, skin sensitivity extremely high,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 17.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Coeliac disease
Condition aggravated
Dysphagia
Eosinophilic oesophagitis
Fatigue
Swelling
Symptomtext
After the first moderna shot on 7/14/21, I experienced extreme fatigue x 3 weeks and my cornea opening up x 2 within the first two weeks after receiving the first dose. I received my second shot on 8/17 and within 48 hrs my cornea opened again, my eosinophilic esophagitis was flared up and my joints were extremely painful. I could not swallow for 3 days due to the esophagus swelling. All of the symptoms I experienced are ones that happen when I am exposed to wheat/gluten. It's like the shot made my body think that I had been exposed. I have had my celiac symptoms and eosinophilic esophagitis well controlled for over two years. And now they are out of control.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Celiac Disease, Eosinophilic Esophagitis
- Andere Medikamente
- prilosec OTC, Budesonide
- Allergien
- Eggs, wheat, milk
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 20.08.2021
- Impfdatum
- 29.07.2021
- Beginn
- 29.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Inflammation
Tachycardia
Symptomtext
SEVERE Tachycardia lasting for a sold 30 minutes before subsiding that randomly for the next 36 hours before completely being resolved. Almost went to ER for further evaluation, would have if symptoms didn't improve at 48 hours. Called a doctor which stated to take Benadryl for possible allergic reaction which helped along with monitoring Blood Pressure, also took Ibuprofen and Tylenol to help with discomfort and inflammation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- Took Blood Pressure at home to for 2 days
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 19.08.2021
- Impfdatum
- 17.08.2021
- Beginn
- 17.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood pressure increased
Fatigue
Headache
Tremor
Symptomtext
I started shaking hard and it lasted for 5 hours. My blood pressure went up to 161/80 and pulse 122. Temp was 100.9 At 11:38 p.m. my temp was 101.9 and my blood pressure was 142/100 pulse 111. I had a terrible headache that lasted until the afternoon of August 18th. My temperature went to 102.1. Today is August 19, 2021 and I feel drained and still have a headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Scleroderma, Stage 3B Chronic Kidney Disease, Fibromyalgia, PSVT, Migraines, GERD, Chronic Pain, Hypertension, Breathing Problems
- Andere Medikamente
- -
- Allergien
- Ibuprofen
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 14.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Back pain
Headache
Injection site erythema
Injection site pruritus
Injection site swelling
Injection site warmth
Pain in extremity
Palpitations
Vaccination complication
Symptomtext
Sore arm: 1-4 days after vacccination Headache: 1 day after vaccination Lower back pain: 1-3 days after vaccination Palpitations: 2-3 days after vaccination (could be anxiety or WPW, not related to vaccine) COVID arm (itchy, swelling, redness, warm): occurred 1 week after vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Wolff Parkinson?s White Syndrome
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 14.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Angiogram
Blood test
Computerised tomogram
Echocardiogram
Epistaxis
Feeling hot
Limb discomfort
Magnetic resonance imaging
Muscular weakness
Paraesthesia
Scan with contrast
Sensory loss
Throat tightness
Ultrasound Doppler
Symptomtext
I was driving and R arm became heavy and very weak. I experienced and overall body heating and tingling sensation. My throat started to close up and my nose started to bleed. R arm weakness and decreased sensation lasted approximately 30 minutes and resolved. Went to ER and was admitted to the hospital for stroke protocol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- 2,0
- Labordaten
- MRI (08/12/21) MRA, MRI carotid with contrast (08/13/2021) Cat scan (08/12/2021) Echocardiogram and with bubble study (08/12/2021) Carotid ultrasound (08/12/21) Bloodwork- 8/12-8/14
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- History of CVA, ulcerative colitis
- Andere Medikamente
- Disodium balsalizide
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 09.08.2021
- 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: ja
Asthenopia
Chills
Dizziness
Dyspnoea
Feeling hot
Heart rate increased
Hypoaesthesia oral
Malaise
Nausea
Painful respiration
Peripheral coldness
Vertigo
Symptomtext
Patient initially described not feeling well. She reported Dizziness, nausea,and painful breathing, shortness of breath, rapid heartbeat, feeling hot with shivers. One cold hand and one warm hand. vertigo, heavy eyes, tongue numbness no rash. Patient was offered and received 50mg Diphenhydramine as an oral suspension. As symptoms got worse, an epipen was administered to right outside thigh. Patient was given alcohol pad to self-swab before administration and a band aid to put on after epipen administration. Patient's symptoms improved dramatically within a couple minutes. Patient was picked up by sister and driven to primary physician after symptoms had largely cleared up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None so far
- Aktuelle Erkrankungen
- None Known
- Vorgeschichte
- None Known
- Andere Medikamente
- None known
- Allergien
- Pineapple was mentioned
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 05.08.2021
- 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: ja
Erholt: nein
Dyspnoea
Heart rate increased
Hypertension
Palpitations
Symptomtext
Patient experienced rapid heart palpitations and difficulty breathing but shortly after she was able to breath. pharmacist called the ambulance , when paramedics came , they checked the patient vitals . her heart beat and blood pressure was slightly high but vitals came down after 15 minutes and when they checked her vitals for the third time. vitals were in normal ranges. patient was asked if she wants to go to the hospital but she refused . paramedics left after patient claimed that she is feeling okay. Minutes after paramedics left patient started to have a rapid heart beat again.so pharmacist called the ambulance for the second time and when they came patient was taking to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 04.08.2021
- Impfdatum
- 13.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Arthralgia
Bone marrow disorder
Condition aggravated
Inappropriate schedule of product administration
Joint injection
Magnetic resonance imaging joint
Pain in extremity
Panic reaction
Tendon rupture
Ultrasound joint
Symptomtext
1st vaccine injection on 5/18/2021 was what I believe to be pretty usual to what I've experienced from others. 2nd Vaccine on 7/13/2021 was ok with just sore arm at first, but I realized by the 2nd or 3rd day that my arm, shoulder and hand were really sore. I had recently been on 1 week of Prednisone and then an Ultrasound guided injection for my right shoulder that has been really needing total replacement for about 2 years. Now this sudden Left shoulder pain is pretty scary to me as I did not 'do' anything to promote the pain (other than the vaccine). I know the pain Too well of my Rt shoulder to know that something was very wrong in my left. I called Dr. who told me that she definitely thought that it was related to the shot and that if it continued she would order an mri. Within 2 days, I recontacted her office about the overall pain exceeding my usual limits. She ordered the mri which was done on 7/30/2021. The results were not only surprising to me but really sent me into panic as well. The report said of a full thickness tear and things about the infraspinatus tendon and something about Bone Marrow. I do not fully understand the report and the only response that I have received from the Dr is that she is inquiring with another Dr, whom I am also a patient (for the Rt Shoulder). I have not heard anything this week yet as to any further testing, or what can be done to improve what is happening. This has put me to being Very Limited as I have depended upon my Left arm/shoulder to accommodate when my Rt cannot. I had previously had NO Pain at all in this arm so the report to me is mind blowing..and quite painful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 07/26/2021 Video visit with Dr. regarding my New Left shoulder pain. 07/30/2021 Completed an MRI (without contrast) ordered by Dr.
- Aktuelle Erkrankungen
- N/K
- Vorgeschichte
- Chronic Pain, L & C spinal issues, Degenerative Disk Disease, Diabetes, RT Shoulder needs total replacement (as of about 2 years ago), Stenosis, Spondylosis, Migraine (worse now), RT Knee (replaces twice 2014/2016 without progress other than some rom), Many cautions regarding digestion of food/meds because of gastric bypass (2005). NEW Left shoulder pain at joint, down arm and into two fingers. Also painful towards back of neck. Never had pain here prior to vaccine. Other pain in Left shoulder and Rt knee are also accentuated steadily.
- Andere Medikamente
- Trulicity, Lantus ,Ambien, Zinc, Magnesium, Serrepatase, Hesperiden, daily vitamin, Theracran, Sumatriptan, Alpha Lipoic Acid, Tramadol, B-12 Injection, D3, and a probiotic P8
- Allergien
- Whole Milk (recent), NSAIDS, Latex, Med Tapes, All 'Cillin" drugs, Statins
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 03.08.2021
- Impfdatum
- 22.07.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Feeling hot
Headache
Heart rate
Heart rate increased
Insomnia
Palpitations
Vaccination complication
Symptomtext
Having a bad reaction/ Still having a bad reaction; Rapid heart rate/ Feels it beating fast; Feels palpitations in her chest; Headache was bad; Feels hot; Cannot catch her breath due to palpitations; Cannot sleep due to palpitations; This spontaneous case was reported by a pharmacist and describes the occurrence of VACCINATION COMPLICATION (Having a bad reaction/ Still having a bad reaction), HEADACHE (Headache was bad), HEART RATE INCREASED (Rapid heart rate/ Feels it beating fast), PALPITATIONS (Feels palpitations in her chest), FEELING HOT (Feels hot), DYSPNOEA (Cannot catch her breath due to palpitations) and INSOMNIA (Cannot sleep due to palpitations) in a 44-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. Concurrent medical conditions included Celiac disease. On 22-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. In July 2021, the patient experienced FEELING HOT (Feels hot) (seriousness criterion life threatening), DYSPNOEA (Cannot catch her breath due to palpitations) (seriousness criterion life threatening) and INSOMNIA (Cannot sleep due to palpitations) (seriousness criterion life threatening). On 22-Jul-2021, the patient experienced HEADACHE (Headache was bad) (seriousness criterion life threatening). On 25-Jul-2021, the patient experienced HEART RATE INCREASED (Rapid heart rate/ Feels it beating fast) (seriousness criterion life threatening) and PALPITATIONS (Feels palpitations in her chest) (seriousness criterion life threatening). On an unknown date, the patient experienced VACCINATION COMPLICATION (Having a bad reaction/ Still having a bad reaction) (seriousness criterion life threatening). The patient was treated with PARACETAMOL (TYLENOL) for Headache, at an unspecified dose and frequency. At the time of the report, VACCINATION COMPLICATION (Having a bad reaction/ Still having a bad reaction) had not resolved and HEADACHE (Headache was bad), HEART RATE INCREASED (Rapid heart rate/ Feels it beating fast), PALPITATIONS (Feels palpitations in her chest), FEELING HOT (Feels hot), DYSPNOEA (Cannot catch her breath due to palpitations) and INSOMNIA (Cannot sleep due to palpitations) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 25-Jul-2021, Heart rate: rapid (High) Rapid. 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 to the pharmacist that she was experienced headache on the first night of the date the vaccine was received which the pharmacist stated was normal but when the headache was bad, the patient took Tylenol. The patient was unable to check her pulse as per the pharmacist as the patient does not have anything to check with but feels the palpitations in her chest. The pharmacist asked to the patient if she need to go to the urgent care and asked if the patient could receive her 2nd dose. No treatment information provided for all the events except Headache. The concomitant medication included blood pressure medications (but was unable to provide names). Company comment:Based on the current available information and temporal association between the use of the product and the start date of these 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 these events, a causal relationship cannot be excluded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210725; Test Name: heart rate; Result Unstructured Data: Rapid
- Aktuelle Erkrankungen
- Celiac disease
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 02.08.2021
- Impfdatum
- 28.07.2021
- Beginn
- 30.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Axillary pain
Burning sensation
Erythema
Herpes zoster
Neck pain
Paraesthesia
Rash
Rash macular
Rash papular
Vaccination complication
Symptomtext
Starting feeling pain in left armpit of arm shot was given on 7/29 on 7/30 I woke up to a small red spot under the arm. On 7/31 spot got bigger and noticed another spot on the other side of same arm pit. On 8/01 red spots became larger, bumpy and more red, burning and tingling sensation. Spots are very painful. On 8/2 I went to emergency road where a doctor took a look and diagnosed me with Shingles, he stated it was due to the ingredients in the moderna shot causing shingles to surface as a reaction. I've never had this before. Never any skin issues like this. And it's very painful.. I now have noticed a red painful mark on the left side of my neck.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/a
- Andere Medikamente
- N/a
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 02.08.2021
- Impfdatum
- 31.07.2021
- Beginn
- 02.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Cough
Fatigue
Oropharyngeal pain
Rhinorrhoea
Symptomtext
About 36 hours after injection, woke up with sore throat, runny nose, dry cough, chest pain and fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hidradenitis suppurativa
- Andere Medikamente
- -
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 02.08.2021
- Impfdatum
- 21.06.2021
- Beginn
- 28.07.2021
- Tage bis Beginn
- 37,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dyspnoea
Headache
Malaise
Nausea
Pain
Pyrexia
SARS-CoV-2 test positive
Vomiting
Symptomtext
On 7/28/21, employee began feeling sick. Symptoms were, nauseous, vomiting, headache, fever, body aches, coughing, shortness breath. OTC medications are being taken. No doctor or hospitalization to date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- PCR test done on 7.28.21 followed by a rapid test on 7.29.21. Rapid test was positive on 7.29.21 followed by positive results for PCR on 8.2.21.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Amlodipine, losartan, hydrochlorothiazide
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 30.07.2021
- Impfdatum
- 30.07.2021
- Beginn
- 30.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Dyspnoea
Symptomtext
CHEST PAIN AND SHORTNESS OF BREATH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- AMITRIPTYLLINE, VIT D, ALBUTEROL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 26.07.2021
- Impfdatum
- 26.07.2021
- Beginn
- 26.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cold sweat
Dizziness
Paraesthesia
Symptomtext
Patient came in for her first dose of Moderna vaccine. After she received her vaccine she was in the waiting area and began to complain of dizziness and stated she felt as if she was going to faint. She also began to complain of arm tingling on the left side. When I went to check her blood pressure, she felt very clammy to the touch. Prior to calling EMS, her blood pressure was taken twice approximately ten minutes apart. The first reading was 93/52 mmHg with a pulse of 45 and the second reading was 93/62 mmHg with a pulse of 68. EMS arrived and monitored her for approximately ten minutes and stated her vitals were beginning to stabilize and she would not need to be transported to a medical facility. I monitored the patient for an additional ten minutes after to this to ensure she felt okay before allowing her to leave.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Not applicable
- Vorgeschichte
- Hypertension, asthma
- Andere Medikamente
- Losartan, hydrochlorothiazide, propranolol. No medications were taken the day of vaccination.
- Allergien
- Ampicillin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 26.07.2021
- Impfdatum
- 22.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Hypoaesthesia
Pain
Tremor
Symptomtext
approximately 22 1/2 hours after receiving first dose of Moderna vaccine, I started having chills and shaking, that lasted about 4 hours, all ten fingertips went numb for about an hour, fever lasted about 4 hours, body aches from head to toe lasted about 12 hours. Took Tylenol every 4 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- covid - still have no taste or smell and had covid on 12/1/2020
- Andere Medikamente
- none
- Allergien
- Alpha Gal allergy, beef, pork and lamb. Sweet potato
- Vorherige Impfungen
- -
- Staat
- VT
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 26.07.2021
- Impfdatum
- 25.07.2021
- Beginn
- 25.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Chest pain
Discomfort
Dysstasia
Exposure during pregnancy
Fall
Feeling abnormal
Laboratory test
Respiration abnormal
Tremor
Uterine contractions during pregnancy
Symptomtext
Pregnant: approximately 37 wks 3 days Due Date: August 11th Injection given. Approximately 15-30 seconds passed. Feeling that something was wrong, lasted only a second before I felt like my breathing was changing. Felt a pressure on all sides of me, heaviness. Each breath became harder to take. Called for help. Tried to stand but could not, fell to floor. Very difficult to get in air at all. Crawled into room with technician who went for emergency supplies. Could not breath. Technician tried to administer one epi-pen, which failed to work. Administered a second. Within 5-10 seconds breathing began to improve. I began to shake uncontrollably. Chest pain /pressure started in center of chest. Unable to move from side of sit up without breathing suffering. I was taken by emergency services to the nearest hospital to make sure breathing/oxygen levels were stable. Taken to Hospital. Contractions started after about 15-20 minutes in the ambulance. The ER ran tests/labwork. I'm unaware of what they are. Once I was deemed stable for transfer, with contractions continuing, I was was transferred to Medical Center to be monitored at Labor and Delivery for potential early labor. I was discharged that evening when labor did not progress.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Mild cough 5 days prior, no other symptoms. Healthy at time of appointment for several days.
- Vorgeschichte
- Hashimoto's Thyroidism Past history of thyroid cancer Celiac Disease Migraines with Aura
- Andere Medikamente
- Unithroid 75 mcg Omeprazole OTC dose Prenatal Vitamin (OLLY)
- Allergien
- Gluten (celiac disease) Mango
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 23.07.2021
- Impfdatum
- 21.07.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood test
Confusional state
Dehydration
Fatigue
Headache
Lethargy
Livedo reticularis
Pain
Pyrexia
Symptomtext
Extremely high fever 105.9, confusion, severe headache, body aches, fatigue, mottling of hands and feet, weakness, lethargy, dehydration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- Routine bloodwork on 7/22/2021
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- PTSD, RLS, psychiatric
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 22.07.2021
- Impfdatum
- 21.07.2021
- Beginn
- 21.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Erythema
Headache
Laboratory test
Muscle tightness
Muscular weakness
Rash
Rash erythematous
Rhinorrhoea
Tremor
Vision blurred
Symptomtext
Arms turned red, back started tightening up, headache, nose started running, blurred vision, red rash covered entire body, shaking and weak legged, went to ER received 3 shots and placed him on meds.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- 1,0
- Labordaten
- Various Test Ran
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Olmesartan Medoxomil 40mg (twice daily) Amlodipine Besylate 10mg (twice daily)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 27.08.2022
- Impfdatum
- 01.07.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 39,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Biopsy skin abnormal
Cellulitis
Depression
Dermatitis
Dermatitis contact
Eczema
Induration
Oedema peripheral
Pain in extremity
Panic disorder
Pruritus
Psoriasis
Symptomtext
Approximately 3 days after second shot I noticed small various sizes of circular lesions on the right hand -approximately 6 later the lesions began to increase in size and started to cause panful itching and sever skin hardening- I attempted various OTC lotions and ointments to alleviate my pain and itching to no avail - now panic and depression started and I immediately sought professional medical attention both phycological and physical attention - the condition has worsened and spread to entire body from head to toe - and as of today I am still seeking and resolution to my chronic condition- I am under the care of a dermatologist who has given me multiple diagnoses such : Psoriasis, Eczema , contact Dermatitis and neurological dermatitis amount
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Skin Biopsy - Cellulitis - Severe Edema of lower legs -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Diabetic - Hypertension - High Cholesterol
- Andere Medikamente
- Lisinopril - Rybelsus - Rosuvastatin - Glipizide - Vitamin D3
- Allergien
- Penicillin
- Vorherige Impfungen
- Pneumonia Vaccine
- Staat
- IL
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 17.05.2022
- Impfdatum
- 12.02.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 50,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Cough
Fatigue
Malaise
Pain
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I showed symptoms of COVID on April 3, 2022. (Chills, cough, runny nose, ache, fatigue.) I called Dr. on April 4. He recommended I take a self COVID test. I did and the result was positive. He prescribed a round of anti virals. I took them for five days and tested negative for COVID after.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Kidney Stone in March 2022.
- Vorgeschichte
- Obesity.
- Andere Medikamente
- Armorthyroid. Lamotrigine.
- Allergien
- Dairy.
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Influenza like illness
Nausea
Pain in extremity
Peripheral swelling
Pyrexia
Symptomtext
A couple of hours after the vaccine I developed a fever, nausea, flu like symptoms, I had swelling, redness and soreness in my arm. I took some Tylenol for my symptoms that lasted for three days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- Codeine; Talwin; Statin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 29.04.2022
- Impfdatum
- 11.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Rash
Tinnitus
Symptomtext
Rash all over for 2 months, tinnitus and headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Antidepressants
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- VI
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 09.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Gastric disorder
Mechanical urticaria
Throat tightness
Symptomtext
about 9 days after my booster (moderna), patient developed dermatographia, tightness in throat, stomach issues. NOTE: i am providing a link to a website where people in the comments have all had a similar reaction. MANY MANY PEOPLE!
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- Not applicable.
- Aktuelle Erkrankungen
- No illnesses at the time, but had Covid 11 months before.
- Vorgeschichte
- High cholesterol
- Andere Medikamente
- Sertraline, Atorvastatin
- Allergien
- Allergic to medications derived from opioids.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 15.04.2022
- Impfdatum
- 22.10.2021
- Beginn
- 24.03.2022
- Tage bis Beginn
- 153,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acne
Bloody discharge
Immunodeficiency
Injection site induration
Injection site reaction
Injection site swelling
Pustule
Scar
Symptomtext
Patient was administered COVID Moderna 0.5ml on 10/22/2021 as his 3rd dose. Patient stated he was immunocompromised because he was on Oztela and agreed to receive the full dose. Prior administrations of Moderna were uneventful. 1 week after his 3rd dose, injection site developed a small pimple that would continue to grow until around 3/17/22. Patient states that it grew to the size of a half dollar and was painful without touching. Around 3/17/2022, it popped on its own and was filled with pus and blood. 3/24/2022, patient showed his PCP the pimple to which the PCP told him that it was nothing to worry about. Patient came to the pharmacy on 4/15/2022 and showed me the remaining scar and hard bump the size of a nickel on the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site induration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Psoriasis
- Andere Medikamente
- Otezla Amlodipine HCTZ
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 29.08.2021
- Beginn
- 31.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Conjunctival defect
Eye inflammation
Malaise
Memory impairment
Pancreatic failure
Visual impairment
Unevaluable event
Symptomtext
08/31/2021, a few days after vaccine I had a rapid change in my vision that they said was age related, I couldn't read signs, articles, etc. Epi membrane was stuck and went to two other specialists that gave me the same diagnosis, which was caused by inflammation. Because of this I believe that it is completely linked to the vaccine. Currently one eye is working as normal after being given steroids for another health complication and one of the eyes, my left eye, is still stuck due to inflammation. If this gets worse there is possibility of surgery and could cause retinal tearing. Over the last month and a half, I have been diagnosed with pancreatic insufficiency, which is causing me stomach discomfort and other issues that come with this diagnosis. Memory has been altered and overall I am not feeling well as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Stool samples led to pancreatic insufficiency
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Fatigue, Hashimoto's Thyroiditis, Sarcoidosis
- Andere Medikamente
- Celebrex
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 14.03.2022
- Impfdatum
- 23.10.2021
- Beginn
- 06.01.2022
- Tage bis Beginn
- 75,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cough
Headache
Paranasal sinus hypersecretion
Respiratory tract congestion
Symptomtext
I got symptoms of headache, sinus drainage, cough, and chest congestion for 3 days and went away. My wife had it at the same time. I could not get a COVID test due to supply issues in my area. I did call my doctor and she stated those are the symptoms but she could not test due to having no tests available.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic Sinus; Chronic Asthma; PVC
- Andere Medikamente
- Finasteride; Levothyroxine; Lopressor; Crestor; Montelukast; Advair; Probiotic; Mineral Supplement
- Allergien
- Clindamycin
- Vorherige Impfungen
- Dose 2 Moderna, sore arm.
- Staat
- VI
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 29.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Biopsy
Hysterectomy
Pruritus
Radiotherapy
Ultrasound scan
Ultrasound scan vagina
Uterine cancer
Vaginal haemorrhage
Symptomtext
I started spotting, blood coming from the vagina. I went to the gynecologist and the first time she didn't do anything. Just a biopsy. I noticed that it got worse, and I went back to her and we did a second biopsy and then she sent me to the lab and they did an ultrasound- microscopic examination. Gyn-Transvaginal U/S. The results that came back is that I had stage 1 uterus cancer. So, I came to the (withheld), and the doctor performed surgery on January 5, 2022 and I had a hysterectomy. And following up with radiation next week. I didn't have any allergies before either and now I'm having allergic reactions to either fish or shellfish. but I was itchy for 3 weeks straight and I'm not sure if that's from surgery or something else. Radiation is a preventative measure so that the cancer doesn't come back.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- 2,0
- Labordaten
- 2 biopsies - indicated the stage 1 uterus cancer Ultrasound Scan after surgery prior to radiation
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Shrimp (after the health event) - itching for 3 weeks straight
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 08.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy test
Blood test
Pruritus
Urticaria
Symptomtext
Hives and itching that are improved with antihistamines
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Allergy blood work results pending 03/01/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- Nka
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 08.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy test
Blood test
Pruritus
Urticaria
Symptomtext
Hives and itching that are improved with antihistamines
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Allergy blood work results pending 03/01/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- Nka
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 29.07.2021
- Beginn
- 29.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Night sweats
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test
Sinusitis
Sneezing
Symptomtext
started sneezing; my sinuses were draining down; kind of felt like I had a sore throat; night sweats; slight fever off and on; night sweats; This spontaneous case was reported by a consumer and describes the occurrence of the first episode of NIGHT SWEATS (night sweats), SNEEZING (started sneezing), SINUSITIS (my sinuses were draining down), OROPHARYNGEAL PAIN (kind of felt like I had a sore throat) and the second episode of NIGHT SWEATS (night sweats) in a 73-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Shortness of breath on 15-Jul-2021, Weakness on 15-Jul-2021, Pain in extremity on 15-Jul-2021 and Nausea on 15-Jul-2021. On 29-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Jul-2021, the patient experienced the first episode of NIGHT SWEATS (night sweats) and PYREXIA (slight fever off and on). On 06-Aug-2021, the patient experienced the second episode of NIGHT SWEATS (night sweats). On 07-Aug-2021, the patient experienced SNEEZING (started sneezing), SINUSITIS (my sinuses were draining down) and OROPHARYNGEAL PAIN (kind of felt like I had a sore throat). At the time of the report, SNEEZING (started sneezing), SINUSITIS (my sinuses were draining down), OROPHARYNGEAL PAIN (kind of felt like I had a sore throat), the last episode of NIGHT SWEATS (night sweats) and PYREXIA (slight fever off and on) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 29-Jul-2021, Body temperature (Unknown-97.5): 98 (High) fever of 98 degree F. On 06-Aug-2021, SARS-CoV-2 test: positive (Positive) tested positive for COVID-19. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant product use was not provided by the reporter. Treatment medication was not provided by the reporter. Company comment: 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
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210729; Test Name: Body temperature; Result Unstructured Data: fever of 98 degree F; Test Date: 20210806; Test Name: COVID-19 Test; Test Result: Positive ; Result Unstructured Data: tested positive for COVID-19
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Nausea; Pain in extremity; Shortness of breath; Weakness
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 01.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Vaccination site pain
Symptomtext
Fuzzy sensation in the arm; Pain at the site of the injection; This spontaneous case was reported by a consumer and describes the occurrence of HYPOAESTHESIA (Fuzzy sensation in the arm) and VACCINATION SITE PAIN (Pain at the site of the injection) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 01-Aug-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 01-Aug-2021, the patient experienced VACCINATION SITE PAIN (Pain at the site of the injection). On 07-Aug-2021, the patient experienced HYPOAESTHESIA (Fuzzy sensation in the arm). On 02-Aug-2021, VACCINATION SITE PAIN (Pain at the site of the injection) had resolved. At the time of the report, HYPOAESTHESIA (Fuzzy sensation in the arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications or treatment details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 30.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Exposure to SARS-CoV-2
Headache
Nasal congestion
SARS-CoV-2 test
Vaccination site inflammation
Symptomtext
Congestion; Vaccination site inflammation; Cough; Exposure to COVID-19; headache; This spontaneous case was reported by a consumer and describes the occurrence of NASAL CONGESTION (Congestion), VACCINATION SITE INFLAMMATION (Vaccination site inflammation ), COUGH (Cough), EXPOSURE TO SARS-COV-2 (Exposure to COVID-19) and HEADACHE (headache) in a 36-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 30-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced NASAL CONGESTION (Congestion), VACCINATION SITE INFLAMMATION (Vaccination site inflammation ), COUGH (Cough), EXPOSURE TO SARS-COV-2 (Exposure to COVID-19) and HEADACHE (headache). The patient was treated with IBUPROFEN for Vaccination site inflammation, at an unspecified dose and frequency. At the time of the report, NASAL CONGESTION (Congestion), VACCINATION SITE INFLAMMATION (Vaccination site inflammation ), COUGH (Cough), EXPOSURE TO SARS-COV-2 (Exposure to COVID-19) and HEADACHE (headache) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 03-Aug-2021, SARS-CoV-2 test: negative (Negative) Negative. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were provided. The patient stated that he had 15 COVID tests in the last 2 years and there were no positive results. The patient also stated that these symptoms will affect his cardiovascular capacity which will affect his job.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210803; Test Name: COVID test; Test Result: Negative ; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 26.07.2020
- Beginn
- 19.07.2021
- Tage bis Beginn
- 358,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Diarrhoea
Symptomtext
Gastric Disturbances; Diarrhea; This spontaneous case was reported by a consumer and describes the occurrence of ABDOMINAL DISCOMFORT (Gastric Disturbances) and DIARRHOEA (Diarrhea) in a 40-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 051C21A and 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 26-Jul-2020, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Jun-2021, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 19-Jul-2021, the patient experienced ABDOMINAL DISCOMFORT (Gastric Disturbances) and DIARRHOEA (Diarrhea). At the time of the report, ABDOMINAL DISCOMFORT (Gastric Disturbances) and DIARRHOEA (Diarrhea) had not resolved. Concomitant product details was not reported. Treatment details was not reported . This case was linked to MOD-2021-270691 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 22.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Fatigue
Symptomtext
Dizziness; Fatigue; This spontaneous case was reported by a consumer and describes the occurrence of DIZZINESS (Dizziness) and FATIGUE (Fatigue) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091d21a) for COVID-19 vaccination. 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 an unknown date, the patient experienced DIZZINESS (Dizziness) and FATIGUE (Fatigue). At the time of the report, DIZZINESS (Dizziness) and FATIGUE (Fatigue) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No Concomitant medications were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 06.10.2021
- Beginn
- 07.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Feeling abnormal
Illness
Impaired work ability
Influenza like illness
Thinking abnormal
Symptomtext
The day after I was sick with flu like symptoms. For 3 weeks following I had severe fatigue and brain fog to the point I could not work. I was very slow to process when someone spoke to me. I could not think clearly. I needed to take naps daily, sometimes twice per day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hoshimoto's disease, Asthma
- Andere Medikamente
- Zolpidem,
- Allergien
- Kiwi, drugs with Sulfa in them, Calcium Carbonate
- Vorherige Impfungen
- I was approximately 9. I am not sure exactly which vaccines. I believe multiple. I got very sick and had to miss school for a w
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 21.02.2022
- Impfdatum
- 27.10.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 24,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Blood immunoglobulin G
Blood test
C-reactive protein increased
Headache
Inflammatory marker increased
Polymyalgia rheumatica
Pyrexia
Red blood cell sedimentation rate increased
Scan
Vertigo
Symptomtext
Acute hip joint pain began on date noted, 3+ weeks after vaccine, gradually appearing in multiple joints, especially shoulders and wrists, accompanied by slight fever, headaches, vertigo. Initially diagnosed as polymyalgia rheumatica with possible giant cell arteritis, but soon mostly ruled out due to limited response to high dose prednisone, which lessened the symptoms a little. Extensive testing has since failed to pinpoint the cause. A neighbor in my small, close-knit community developed almost identical symptoms starting the day after he received his 3rd vaccine dose. His doctors have also failed to pinpoint the cause.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Multiple blood tests, seeking possible infections or other sources of inflamation, and scans found nothing remarkable except acutely elevated inflammatory markers (CRP and ESR), and most recently, elevated immunoglobulin G subclass 4.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Irregular heartbeat (benign PVC) Occasional joint pain, likely osteoarthritis, mostly one at a time, generally overcome with physical therapy. Most pronounced for years, and exacerbated in May 2021, in right shoulder.
- Andere Medikamente
- Multivitamin, D3 and C, CoQ10, glucosamine
- Allergien
- No
- Vorherige Impfungen
- Mild discomfort, fever, aches, for up to two days after Moderna vaccines
- Staat
- NC
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 30.09.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Headache
Magnetic resonance imaging
Muscle spasms
Nausea
Vomiting
Symptomtext
muscle spasms, headaches, naseau, vomiting
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- mri
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 09.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pruritus
Rash
Symptomtext
Patient called the pharmacy on 12-10-2021 to report that she was having itching and a rash formed. She was advised to contact her prescriber if the symptoms got worse or changed. She asked that we just note it in her file. If symptoms did not improve in 24-48 hours she should see her doctor. She did end up seeing 2 different prescribers at an Urgent Care facility and was provided prescription treatment. On 12-13-2021 she was prescribed by HCP Zyrtec 10mg daily and Prednisone 40mg daily for 5 days. She followed up with Dr. at the same Urgent Care on 12-20-2021 and was provided a Medrol DosePak and Atarax 25mg three times per day if needed for itching.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- None Reported
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- No Known Allergies
- Vorherige Impfungen
- Felt Faint or Dizzy
- Staat
- TN
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 13.11.2021
- Beginn
- 21.11.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dermatologic examination
Mechanical urticaria
Pruritus
Urticaria
Symptomtext
Contact urticaria/hives all over the body with intense itching that lasted for 10 days. Following the itching and full body hives, dermatographia has been a lasting issue that has not subsided (and still persists over 2 months post-vaccination)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- Dermatology visit 12/06/2021, confirmed dermatographia diagnosis.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Tri sprintec oral contraceptive
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 18.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Drainage
Headache
Impaired work ability
Nausea
Symptomtext
After receiving the vaccine I had headaches. Then I had sensitivity and nausea when I was close to my period. One day I couldn't work because they were so severe. I also had drainage and dizziness. I took migraine medication, but they didn't work. The headaches are so severe. I have an upcoming appointment scheduled for a MRI.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Aspirin.
- Allergien
- Reglan.
- Vorherige Impfungen
- COVID (2nd dose), I had a fever, chills, body aches, nausea, vomiting, and neck stiffness (1/26/2021).
- Staat
- MN
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 16.12.2021
- Beginn
- 17.01.2022
- Tage bis Beginn
- 32,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Abdominal pain
COVID-19
Chills
Clostridium test positive
Dysphonia
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
Hospitalized abdominal pain, possible early appendicitis, sore throat, fever, chills, and voice changes and positive COVID and positive C difficile, also COVID positive in October prior to completion of vaccine series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 04.01.2022
- 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: ja
Axillary pain
Balance disorder
Chills
Decreased appetite
Diarrhoea
Dizziness
Fatigue
Headache
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Injection site warmth
Myalgia
Nausea
Pyrexia
Vertigo
Symptomtext
Fever, muscle aches, & left axillary pain within 4-6 hours of injection. Fevers 101-102F, chills, extreme fatigue, headache, nausea, diarrhea, lack of appetite, & worsening myalgia extending from 10/13/21-10/15/21. On evening of 10/15 I began experiencing slight dizziness which dissipated before going to bed, but then noticed a golfball sized, round, pink, tender, area noted at injection site. The next morning the site enlarged to slightly smaller than tennis ball sized, now warm to the touch, pink-red, swelling, and continued to be itchy & tender, not completely disappearing until 10/26. On Saturday morning 10/16/21, I began experiencing worsening dizziness & headache, to the point I was unable to look downward or turn my head more than a couple degrees side to side without the room spinning and feeling off balance.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Allergies to Amoxicillin, Sulfa, Bactrim, Erythromycin
- Vorherige Impfungen
- -
- Staat
- VI
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 21.12.2021
- Impfdatum
- 11.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Rash macular
Urticaria
Symptomtext
Two weeks after receiving the booster vaccine I developed hives. They would pop up, be red, bumpy and itchy for about a half hour, then go away. I went on steroids for 5 days, which made it good, but as soon as I came off of them, the hives were back. I would have a flair up in the morning, be good at work all day, then they would come back out between 5:30 and 7:00 in the evening. I was taking Benadryl to get through the night for a few weeks, then I went to my primary doctor on 12-14-21. She advised me to switch to Zyrtec D, which has been amazing, for one week then come off of it, that would be today. I have had some red splotches develop while on the Zyrtec, but it has not been itchy. The reason I believe it may be from the booster shot, is because 3 other people in my office who received the booster on the same day are going through the same symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Daily Vitamen
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Symptomtext
Head to toe, full body itchiness and rash
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ocp, spironolactone
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 17.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Chills
Influenza like illness
Oedema peripheral
Pain
Symptomtext
SWELLING AND SORENESS UNDER ARMPIT. FLU LIKE SYMPTOMS, CHILLS, BODY ACHES
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 05.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amnesia
Pyrexia
Symptomtext
102 degree fever for 3 days, short term memory loss sustained until present
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 06.11.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 30,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
No adverse event
Pain in extremity
Symptomtext
No adverse event, patient came for second vaccine and identified pfizer should be primary. Contacted CDC Guidelines for notification and direction. Directed to give second dose pfizer. Patient had no reaction to moderna dose. Only sore arm on 11/07/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- no known
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 02.11.2021
- Beginn
- 21.11.2021
- Tage bis Beginn
- 19,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood test normal
Dysphagia
Influenza virus test negative
Lymphadenopathy
Oropharyngeal pain
Pain
Pyrexia
SARS-CoV-2 test negative
Streptococcus test negative
Symptomtext
First thing I noticed were body aches, second thing I noticed was a sore throat causing trouble swallowing, third thing I noticed was a fever starting at around 99 but increasing to 102. My glands on my neck were very swollen. This went on until about 11/27. I went to the doctor first on 11/23 and received a flu, COVID and strep tests. On 11/24 I went to see my endocrinologist because I wanted bloodwork done.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- All tests came back negative for anything. Blood work came back with nothing as well.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Nogels in lung Multinoginal HO fibulation intermittent
- Andere Medikamente
- Tylenol PM Align probiotic Vit D3 Zetia Flecainide Metoprolol Levothyroxine
- Allergien
- Penicillin Shellfish Iodine
- Vorherige Impfungen
- Flu shot- got the flu after
- Staat
- NY
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 12.10.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Musculoskeletal stiffness
Pain in extremity
Symptomtext
Stiffness in both legs; Achiness in both legs; This spontaneous case was reported by a consumer and describes the occurrence of MUSCULOSKELETAL STIFFNESS (Stiffness in both legs) and PAIN IN EXTREMITY (Achiness in both legs) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) 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) 1 dosage form. On 15-Oct-2021, the patient experienced MUSCULOSKELETAL STIFFNESS (Stiffness in both legs) and PAIN IN EXTREMITY (Achiness in both legs). At the time of the report, MUSCULOSKELETAL STIFFNESS (Stiffness in both legs) and PAIN IN EXTREMITY (Achiness in both legs) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Patient was taking other medications. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Joint stiffness
Symptomtext
Stiff sore joints in fingers. Both hands.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- I did mention this to my doctor. She said that one of the doctors that worked there had the same thing happen to her, However hers only lasted a day and resolved. Mine has not Resolved.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 26.11.2021
- Impfdatum
- 19.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 4,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
4 days after vaccination I developed a rash that looks like eczema at these locations: - right neck and ear - right hand over thumb between pinky fingers - back of upper left leg - genital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- after 1st does, fatigue flue symptoms 2 days; after 2nd dose 4/30, prolonged fatigue (8 weeks), dizziness, tinnitus
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 24.11.2021
- Impfdatum
- 13.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Accidental overdose
Influenza like illness
Pain
Symptomtext
This spontaneous case was reported by an other health care professional and describes the occurrence of INFLUENZA LIKE ILLNESS (Light flu like symptoms), PAIN (Little achy) and ACCIDENTAL OVERDOSE (5 mL administered instead of 0.5 mL as 1st dose) in a 22-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 5 milliliter. On 13-Nov-2021, the patient experienced ACCIDENTAL OVERDOSE (5 mL administered instead of 0.5 mL as 1st dose). On 14-Nov-2021, the patient experienced INFLUENZA LIKE ILLNESS (Light flu like symptoms) and PAIN (Little achy). On 13-Nov-2021, ACCIDENTAL OVERDOSE (5 mL administered instead of 0.5 mL as 1st dose) had resolved. On 15-Nov-2021, INFLUENZA LIKE ILLNESS (Light flu like symptoms) and PAIN (Little achy) had resolved. 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 provided by the reporter.No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- -
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Malaise
Pain
Symptomtext
Evening on Monday the 8, I wasn't feeling well. In bed 7p. During that night and all day Tues I had chills, aches, pains, even my hair hurt. Stayed in bed all day Tuesday, up for a bowl of soup, back to bed. I didn't vomit but was too sick to go anyplace. Wednesday morning I was fine, like nothing happened. What a turn around. I had no reaction to the first 2 shots. Just know I will not get another booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none got my flu shot Oct. 14,2021
- Vorgeschichte
- none
- Andere Medikamente
- Crestor/ Synthroid taken 5a.
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 16.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cold sweat
Dizziness
Fall
Flushing
Headache
Photophobia
Tinnitus
Symptomtext
severe headache with light sensitivity and ear ringing. lightheaded, dizzy, clammy, flush and collapsed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breast swelling
C-reactive protein
Fatigue
Full blood count
Headache
Lymphadenopathy
Neck pain
Oedema peripheral
Pyrexia
Rash macular
Supraclavicular fossa pain
Symptomtext
Persistent fevers (Tmax 102.3) for 3 days, severe fatigue, headaches. Day 2: swelling and pain in R axilla, R breast. Day 3: Right supraclavicular and R neck pain/lymphadenopathy also with skin reaction of red blotches on R upper anterior arm and R lateral breast
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- CBC, sed rate and C-reactive protein pending (11/16/21)
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- allergic rhinitis reactive airway disease mixed connective tissue disease
- Andere Medikamente
- cetirizine montelukast venlafaxine ER 37.5 mg
- Allergien
- lactose intolerance
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 86,0
- Geschlecht
- M
- Eingang
- 15.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Back pain
Injection site pain
Pain
Symptomtext
Pt received severe pain in the shoulder at the injection site. He also had severe shooting back pain at the same time, which lasted for roughly 1/2 hour.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Amlodipine 10mg & Metoprolol ER 50mg
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 13.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 10.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abnormal sensation in eye
Balance disorder
Chest discomfort
Dizziness
Gait disturbance
Headache
Interchange of vaccine products
Symptomtext
Had Pfizer for initial 2 doses with Moderna as a booster 6 months later than 2nd Pfizer shot. Dizziness, stumbling, headache, chest discomfort, eyes felt funny and off balance. Very strong for 6+ hours then slightly still affecting me 2 days later especially the off balance dizziness part.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Magnesium Vitamin D Adrenal support B6
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 92,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Cellulitis
Extra dose administered
Hypersensitivity
Injection site erythema
Injection site infection
Injection site pain
Injection site pruritus
Injection site swelling
Symptomtext
Just below the injection site it was redness and slight swelling in the upper arm. The very next day the swelling went completely down her arm to elbow. It was itchy and red. The doctor said it was fluid, allergic reaction, and cellulitis of the left arm. It was an infection that was swollen and painful. She was prescribed Bactrim to take one tablet twice daily for seven days. She started it on November 7th, 2021. Triamcinolone was prescribed to relieve the itching. The was no reaction to the first two.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic Obstructive Pulmonary Disease Asthma Atrial Fibrillation Congestive Heart Failure Glaucoma Hand and Feet Neuropathy Hyperthyroidism Arthritis
- Andere Medikamente
- Lipitor Plavix Celebrex Diltiazem Eliquis Eszopiclone Pochlor Omeprazole Olmesartan Thyroxine Advair Proair Spiriva Alphagan P Latanoprost Systain Gel Drops Multivitamin Vitamin D Calcium Bactrim Steroidal Cream Triamcinolone
- Allergien
- Lactose Intolerant Black Pepper Clarithromycin Azithromycin Codeine Keflex Erolinta
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 09.11.2021
- Impfdatum
- 23.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 5,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Gastrointestinal inflammation
Laboratory test normal
Leukoderma
Pruritus
Stool analysis abnormal
Urticaria
Symptomtext
I had diarrhea on October 28th, I'm on day 13 of liquid stools. I have never had diarrhea. I have isolated hives in my knees and intense itching with hives. Two days later I had intense itching on my knees. I haven't had any further issues with hives. I saw a doctor and they noted that I had an inflammatory response in my intestines. I had a positive Leukoderma. I've been taking over the counter Imodium.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- I had a few laboratory test and they came back fine Stool Sample-Showed I have Fecal Lactoferrin
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension Sleep Apnea
- Andere Medikamente
- Herbacerton 300mgs-1 time daily in the morning Amlodipine Besylate 5mg at night Hydrochlorothiazide 25mgs in the morning Metoprolol 25mgs at night Omeprazole 25mg at night Zoloft 50mgs in the morning Vitamin D3 Calcium Multivitamins once
- Allergien
- Penicillin
- Vorherige Impfungen
- I got COVID-19 Arm from my dose 1 02/18/2021
- Staat
- IA
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 08.11.2021
- Impfdatum
- 21.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cough
Extra dose administered
Oropharyngeal pain
Rhinorrhoea
Symptomtext
I had cough, sore throat, and a running nose. I still have these symptoms and it has been a week today. I have not been to the doctor about this.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 06.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Injection site erythema
Injection site mass
Injection site pain
Injection site pruritus
Injection site swelling
Symptomtext
Patient received Moderna booster dose on Wednesday, 11/3. Called pharmacy on Saturday, 11/6 at 11:20 am to complain that the injection site was still very itchy, tender, red and swollen, with a lumpy feeling. Patient said had been icing the arm and applying Calamine, but wanted advisement because still itchy and swollen. Pharmacist on duty suggested to take ibuprofen, but patient said unable to since has stomach issues; pharmacist then suggested to take Tylenol for the tenderness and Benadryl for the itching. Pharmacist also advised to continue monitoring her arm and if it got worse to contact her provider.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Did not discuss
- Vorgeschichte
- Did not discuss
- Andere Medikamente
- Did not discuss
- Allergien
- Did not discuss
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 04.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Injection site warmth
Pain
Pruritus
Symptomtext
red, warm area (about 3 x 4 inches) around the injection site, with some itching and soreness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None. I did not report this to the doctor as it sounds like a common reaction, but thought you would want to track reactions to the booster.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- obesity, a-fib
- Andere Medikamente
- lisinopril, omeprezole, levothoraxine, rusuvestatin,cartex, flecanide, MetFormin
- Allergien
- medical adhesive
- Vorherige Impfungen
- mild fever and chills after 2nd dose of Moderna that lasted only 4 hours.
- Staat
- NC
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 04.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Feeling cold
Symptomtext
I experience some chills after I received my booster, I just was very very cold. Nothing really worked for it, that evening I was fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Arthritis
- Andere Medikamente
- Rosuvastatin Mirtazapine Ambien Naproxen Allergy Pill Cetirizine Aspirin Prilosec Mens Vitamins Calcium Vitamin D Trimeric Flaxseed Oil Fish oil
- Allergien
- Outdoor Allergies
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 18.02.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 257,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Chills
Cough
Exposure to SARS-CoV-2
Headache
Neck pain
Rhinorrhoea
Upper respiratory tract infection
Symptomtext
The patient presents with URI symptoms for Yesterday after getting his booster shot. Symptoms include headache, cough, runny nose, chills, shoulder. neck and back pain. starting on 11/2/21. Received Moderna booster on 11/2/21. Wife recently tested positive for COVID (last week)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- giant cell tumor, history of psoriasis
- Andere Medikamente
- naproxen; Folic acidl Methotrexatel Prednisone; humira; Lisinopril
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 02.11.2021
- Impfdatum
- 02.10.2021
- Beginn
- 16.10.2021
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aphonia
Blood test
Computerised tomogram abnormal
Fatigue
Lymph node pain
Lymphadenitis
Lymphadenopathy
Night sweats
Weight decreased
Symptomtext
Starting on 10/16/2021 I had swollen lymph nodes on the right side on my jaw and back of the scalp. CT scan showed huge inflamed lymph nodes. They were very tender and sore to the touch. It lasted for a week. I lost 10 pounds. Lost voice and easily fatigued. Also had terrible night sweats.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- CT Scan Blood work
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Cancer Diabetes Hypertension
- Andere Medikamente
- Atenolol Valsartan Atarvatan Doxepin Metformin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 30.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Rash
Urticaria
Symptomtext
Patient stated that after her first Moderna dose, she had some mild rash around injection site. After second dose, she reported to pharmacy last night that she had a severe reaction to vaccine. She had to go to the ER and get medications. She had a widespread rash that extended down her arm, onto her back, and up onto her neck/throat. The rash was pink with noticeable red welts throughout. The patient still had the rash visible on 10/29/21 when she came into the store to discuss.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- She had mild rash after first moderna dose
- Staat
- NV
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 30.10.2021
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Symptomtext
headache that is bothering her/ a middle headache on the day of the vaccination but it went away; This spontaneous case was reported by a consumer and describes the occurrence of HEADACHE (headache that is bothering her/ a middle headache on the day of the vaccination but it went away) in a 64-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091d21a) for COVID-19 vaccination. No Medical History information was reported. On 21-Oct-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 21-Oct-2021, the patient experienced HEADACHE (headache that is bothering her/ a middle headache on the day of the vaccination but it went away). On 21-Oct-2021, HEADACHE (headache that is bothering her/ a middle headache on the day of the vaccination but it went away) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Relevant concomitant medications were not reported. Treatment medication information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Lymphadenopathy
Pruritus
Symptomtext
Patient called 10/29/21 and said she started itching on 10/28/21 and that she had a knot on arm by left breast and was red. This was not at injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 29.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Injection site erythema
Injection site swelling
Injection site warmth
Myalgia
Pyrexia
Symptomtext
Upon waking the morning after vaccination, patient discovered the injection site was raised about 1.5 inches, red, and warm to the touch within a four inch diameter surrounding deltoid. The exact injection site had a "white dot." The area has slowly started to return to normal but is still somewhat raised, red, and warm to the touch (4 days post injection). Patient also experienced muscle aches and chills throughout entire body for 24 hours. Patient experienced a low-grade fever (Max: 99 degrees) during the morning of 10/26/2021, resolved by afternoon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Tylenol 500mg (as needed for pain); Multivitamin; Vitamin D3
- Allergien
- -
- Vorherige Impfungen
- Lethargy.
- Staat
- CO
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 28.10.2021
- Impfdatum
- 25.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dysuria
Headache
Influenza like illness
Myalgia
Pain of skin
Pollakiuria
Pyrexia
Sleep disorder
Symptomtext
Fever 101 ? Chills ? Muscle ache and headache ? Flu-like symptoms SKIN HURT. It hurt to wear clothes and to lie down on the bed. I had to urinate frequently a teaspoon or so but it was painful enough to wake me up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- ?
- Vorgeschichte
- Asthma, psoriasis
- Andere Medikamente
- Levothyroxine 0.075 mg Montelukast 10 mg Otezla 30 mg 2 x per day Vitamins A, B, C, D Fish Oil
- Allergien
- Contrast Dye
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 26.10.2021
- Impfdatum
- 04.10.2021
- Beginn
- 01.10.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site erythema
Vaccination site pain
Vaccination site warmth
Symptomtext
a couple of days later "hot"; red on the arm she got the shot; 10 days after she got a reaction on the arm she got the shot:sore; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE WARMTH (a couple of days later "hot"), VACCINATION SITE ERYTHEMA (red on the arm she got the shot) and VACCINATION SITE PAIN (10 days after she got a reaction on the arm she got the shot:sore) in a 24-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No medical history was provided by the reporter. Concomitant products included ORAL CONTRACEPTIVE NOS for an unknown indication. On 04-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In October 2021, the patient experienced VACCINATION SITE WARMTH (a couple of days later "hot"), VACCINATION SITE ERYTHEMA (red on the arm she got the shot) and VACCINATION SITE PAIN (10 days after she got a reaction on the arm she got the shot:sore). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) for Adverse event, at an unspecified dose and frequency. At the time of the report, VACCINATION SITE WARMTH (a couple of days later "hot"), VACCINATION SITE ERYTHEMA (red on the arm she got the shot) and VACCINATION SITE PAIN (10 days after she got a reaction on the arm she got the shot:sore) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Patient reported that she got a reaction 'red and sore' 10 days after getting the shot and a couple of days later, she reported it being 'hot'. Patient was also treated with an unspecified antihistamine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- ORAL CONTRACEPTIVE NOS
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 25.10.2021
- Impfdatum
- 12.10.2021
- Beginn
- 12.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Pain in extremity
Vaccination complication
Symptomtext
Reaction unspecified to the 3 shots; Got 3rd dose and is not immunocompromised; They had arm pain pretty immediate, the same day; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (They had arm pain pretty immediate, the same day), VACCINATION COMPLICATION (Reaction unspecified to the 3 shots) and EXTRA DOSE ADMINISTERED (Got 3rd dose and is not immunocompromised) in an 87-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 12-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Oct-2021, the patient experienced PAIN IN EXTREMITY (They had arm pain pretty immediate, the same day) and EXTRA DOSE ADMINISTERED (Got 3rd dose and is not immunocompromised). On an unknown date, the patient experienced VACCINATION COMPLICATION (Reaction unspecified to the 3 shots). On 12-Oct-2021, EXTRA DOSE ADMINISTERED (Got 3rd dose and is not immunocompromised) had resolved. At the time of the report, PAIN IN EXTREMITY (They had arm pain pretty immediate, the same day) and VACCINATION COMPLICATION (Reaction unspecified to the 3 shots) outcome was unknown. Concomitant product use was not provided by the reporter. Treatment information was not provided by the reporter. This case was linked to MOD-2021-354077, MOD-2021-354097, MOD-2021-353213 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 15-Oct-2021: Significant follow up contains added Batch number.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ND
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 25.10.2021
- Impfdatum
- 16.10.2021
- Beginn
- 18.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Pain
Platelet count decreased
Pyrexia
Thrombocytopenia
Symptomtext
Patient reports thrombocytopenia of 6500 and was hospitalized.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 24.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 23.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Back pain
Balance disorder
Extra dose administered
Gait inability
Malaise
Vaccine positive rechallenge
Symptomtext
Extreme back pain, general feeling of severe illness, weakness with inability to walk unaided, near collapse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- Advair, Flonase, Zyrtec, Simvastatin, Lexapro, low dose aspirin, vitamins C D B12 and multivitamin, fish oil, CoQ 10, calcium, melatonin.
- Allergien
- Demerol
- Vorherige Impfungen
- Same but less severe. 79. 03/05/2021. COVID19.Moderna #2 in series.
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 21.10.2021
- Impfdatum
- 08.10.2021
- Beginn
- 09.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Abdominal distension
Arthralgia
Blood test
Headache
Myalgia
Pyrexia
Symptomtext
I had Severe side effects that lasted about a week, I have abodominal bloated with discomfort, low-grade fever 99 everyday on and off for two weeks ,headache on and off for two weeks now. Legs Muscle aches and hip joint pain. Doctors gave me dictclomine and was referee to GI specialist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Blood work 10/16
- Aktuelle Erkrankungen
- I had COVID 1st day of symptoms 7/30/2021 positive test results 08/02/2021. Was still experiencing some minor affects
- Vorgeschichte
- Lower back problem
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 20.10.2021
- Impfdatum
- 20.10.2021
- Beginn
- 20.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chills
Symptomtext
EMT1 on scene Immediately EMT3 on scene Immediately MA- on scene Immediately 1522 911 called Vitals started 1523 0.3ml Epi given in right quad 1525 Oxygen Started 15lbm via NRB 1527 vitals finished 100% O2Sat- 118 bpm- 170/90 BP 1528 Patient laid down with Chills 1530 Ambulance on scene 1535 BP 152/72 1538 Ambulance off Scene and begin transfer to Medical Center
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- HTN, High Cholesterol, L knee surgery
- Andere Medikamente
- Simvastatin, Aspirin
- Allergien
- Severe Allergies, Shellfish, Prior flu shot anaphylactic shock with hospitalization.
- Vorherige Impfungen
- Flu Vaccination
- Staat
- TX
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 20.10.2021
- 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
Fatigue
Headache
Pain
Pain in extremity
Pyrexia
Symptomtext
He got a low grade fever 100.9, headaches, body aches and fatigue that lasted a few days. He slept it off and took some Tylenol at 10pm that evening when he woke up after 5 hours. Still has a sore arm but is beginning to feel better today.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- immunocompromised
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 19.10.2021
- Impfdatum
- 19.10.2021
- Beginn
- 19.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Symptomtext
Sweats and dizzy for 30 mins and went away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Bystolic 5mg Lisinopril 5mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 18.10.2021
- Impfdatum
- 15.10.2021
- Beginn
- 17.10.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Injection site pain
Injection site reaction
Rash macular
Symptomtext
After the 2nd shot on 10/15, I had a bad headache on 10/16 and 10/17. On 10/17 my arm had red blotches going down to my elbow underneath the injection site and hurt like bad bruises.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- 50 mg levothyroxine, prenatal vitamin, fish oil vitamin, and sunflower lecithin for breastfeeding
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 18.10.2021
- Impfdatum
- 09.09.2021
- Beginn
- 08.10.2021
- Tage bis Beginn
- 29,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site erythema
Vaccination site pain
Vaccination site swelling
Vaccination site warmth
Symptomtext
arm was warm, kind like hot; got their arm swollen/gotten a bit bigger down their arm/The arm i less swollen now; The arm i less swollen now but it was a little sore; got their arm red/and red/blachy/maybe could be a blood clot; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE WARMTH (arm was warm, kind like hot), VACCINATION SITE SWELLING (got their arm swollen/gotten a bit bigger down their arm/The arm i less swollen now), VACCINATION SITE PAIN (The arm i less swollen now but it was a little sore) and VACCINATION SITE ERYTHEMA (got their arm red/and red/blachy/maybe could be a blood clot) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 076c21a and 091d21a) for COVID-19 vaccination. No medical history was provided by the reporter. Concomitant products included MULTIVITAMIN [VITAMINS NOS] for an unknown indication. On 09-Sep-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 07-Oct-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 08-Oct-2021, the patient experienced VACCINATION SITE WARMTH (arm was warm, kind like hot), VACCINATION SITE SWELLING (got their arm swollen/gotten a bit bigger down their arm/The arm i less swollen now), VACCINATION SITE PAIN (The arm i less swollen now but it was a little sore) and VACCINATION SITE ERYTHEMA (got their arm red/and red/blachy/maybe could be a blood clot). The patient was treated with IBUPROFEN at an unspecified dose and frequency. At the time of the report, VACCINATION SITE WARMTH (arm was warm, kind like hot), VACCINATION SITE PAIN (The arm i less swollen now but it was a little sore) and VACCINATION SITE ERYTHEMA (got their arm red/and red/blachy/maybe could be a blood clot) outcome was unknown and VACCINATION SITE SWELLING (got their arm swollen/gotten a bit bigger down their arm/The arm i less swollen now) was resolving. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Treatment information also included ice.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- MULTIVITAMIN [VITAMINS NOS]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- 15.07.2021
- Beginn
- 16.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Intentional dose omission
Lung disorder
SARS-CoV-2 test
Tooth infection
Vaccination complication
Symptomtext
caller stated he decided not to receive the second dose in the series; feeling tired/in bed for 4 days; he had a reaction; lungs started feeling weird/ lungs were filled with fluid/lungs had a sloshy feeling; infected tooth; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (he had a reaction), LUNG DISORDER (lungs started feeling weird/ lungs were filled with fluid/lungs had a sloshy feeling), TOOTH INFECTION (infected tooth), INTENTIONAL DOSE OMISSION (caller stated he decided not to receive the second dose in the series) and FATIGUE (feeling tired/in bed for 4 days) in a 65-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The patient's past medical history included Walking pneumonia in 1992. Concurrent medical conditions included Asthma. On 15-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In 2021, the patient experienced TOOTH INFECTION (infected tooth). On 16-Jul-2021, the patient experienced VACCINATION COMPLICATION (he had a reaction), LUNG DISORDER (lungs started feeling weird/ lungs were filled with fluid/lungs had a sloshy feeling) and FATIGUE (feeling tired/in bed for 4 days). On an unknown date, the patient experienced INTENTIONAL DOSE OMISSION (caller stated he decided not to receive the second dose in the series). The patient was treated with NAPROXEN SODIUM (ALEVE) in 2021 for Pain, at an unspecified dose and frequency. On 20-Jul-2021, FATIGUE (feeling tired/in bed for 4 days) had resolved. At the time of the report, VACCINATION COMPLICATION (he had a reaction) outcome was unknown and LUNG DISORDER (lungs started feeling weird/ lungs were filled with fluid/lungs had a sloshy feeling), TOOTH INFECTION (infected tooth) and INTENTIONAL DOSE OMISSION (caller stated he decided not to receive the second dose in the series) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: negative (Negative) Negative. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were reported. It was reported that, for treatment, the patient used his asthma inhalers (name not reported) frequently and took steroid pills daily. About a month ago or so, the caller also reported an infected tooth and he had to have the tooth pulled out. The caller mentioned he cannot tolerate chilis. The caller stated that he was a healthy individual. Stated that he just recently had a COVID-19 test and it was negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Name: Covid-19 test; Test Result: Negative; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- Asthma.
- Vorgeschichte
- Medical History/Concurrent Conditions: Walking pneumonia.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 16.10.2021
- Impfdatum
- 23.07.2021
- Beginn
- 02.10.2021
- Tage bis Beginn
- 71,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Pain in extremity
Product administration error
Symptomtext
receiving 3rd dose of Moderna instead of flu shot; Sore Arm; Headache; This spontaneous case was reported by a consumer and describes the occurrence of PRODUCT ADMINISTRATION ERROR (receiving 3rd dose of Moderna instead of flu shot), PAIN IN EXTREMITY (Sore Arm) and HEADACHE (Headache) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 049E21A., 049E21A and 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 02-Oct-2021, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 02-Oct-2021, the patient experienced PAIN IN EXTREMITY (Sore Arm) and HEADACHE (Headache). On an unknown date, the patient experienced PRODUCT ADMINISTRATION ERROR (receiving 3rd dose of Moderna instead of flu shot). At the time of the report, PRODUCT ADMINISTRATION ERROR (receiving 3rd dose of Moderna instead of flu shot) had resolved and PAIN IN EXTREMITY (Sore Arm) and HEADACHE (Headache) outcome was unknown. 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. This case was linked to MOD-2021-340958 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 04-Oct-2021: follow-up received: Added event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 16.10.2021
- Impfdatum
- 23.07.2021
- Beginn
- 22.08.2021
- Tage bis Beginn
- 30,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling abnormal
Pyrexia
Symptomtext
Felt really bad/felt worse for about 24 hours; fever for about 24 hours; This spontaneous case was reported by a consumer and describes the occurrence of FEELING ABNORMAL (Felt really bad/felt worse for about 24 hours) and PYREXIA (fever for about 24 hours) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 049E21A and 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 22-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 22-Aug-2021, the patient experienced FEELING ABNORMAL (Felt really bad/felt worse for about 24 hours) and PYREXIA (fever for about 24 hours). On 23-Aug-2021, FEELING ABNORMAL (Felt really bad/felt worse for about 24 hours) and PYREXIA (fever for about 24 hours) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medications were not reported. Treatment information include ibuprofen. This case was linked to MOD-2021-341011 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 16.10.2021
- Impfdatum
- 29.07.2021
- Beginn
- 29.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Disturbance in attention
Fatigue
Insomnia
Pyrexia
Tinnitus
Symptomtext
Disrupts sleep; disrupts concentration on daily activities; fatigue; fever (102); ringing in ear getting worse(louder)/ increased; This spontaneous case was reported by a consumer and describes the occurrence of TINNITUS (ringing in ear getting worse(louder)/ increased), INSOMNIA (Disrupts sleep), DISTURBANCE IN ATTENTION (disrupts concentration on daily activities), FATIGUE (fatigue) and PYREXIA (fever (102)) in a 77-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. Concurrent medical conditions included Sulfonamide allergy (Allergic to sulfa antibiotics.), Allergic reaction to analgesics (Allergic to drug Codeine.), Hypertension since 2009, Hyperlipidemia since 2009, Hypothyroidism since 2009 and Tinnitus (Mild tinnitus) since 1978. Concomitant products included ROSUVASTATINE [ROSUVASTATIN] from 2009 to an unknown date for Hyperlipidemia, HYDROCHLOROTHIAZIDE from 2009 to an unknown date, BENAZEPRIL from 2009 to an unknown date and AMLODIPINE from 2009 to an unknown date for Hypertension, LEVOTHYROXINE from 2009 to an unknown date for Hypothyroidism. On 29-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 29-Jul-2021, the patient experienced TINNITUS (ringing in ear getting worse(louder)/ increased). On 28-Aug-2021, the patient experienced FATIGUE (fatigue) and PYREXIA (fever (102)). On an unknown date, the patient experienced INSOMNIA (Disrupts sleep) and DISTURBANCE IN ATTENTION (disrupts concentration on daily activities). On 29-Aug-2021, FATIGUE (fatigue) and PYREXIA (fever (102)) had resolved. At the time of the report, TINNITUS (ringing in ear getting worse(louder)/ increased) had not resolved and INSOMNIA (Disrupts sleep) and DISTURBANCE IN ATTENTION (disrupts concentration on daily activities) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 28-Aug-2021, Body temperature: 102 (High) Fever 102 F. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. It was reported that the patient had mild tinnitus from the past years but the intensity was increased just a few hours after the first dose of vaccination Treatment information was not reported Most recent FOLLOW-UP information incorporated above includes: On 17-Aug-2021: Non-Significant FU, updated reporter information. On 07-Oct-2021: Significant follow up received included patient demographics, relevant Medical history, lab investigation Concomitant medications; Outcome of the event tinnitus updated from unknown to not recovered; Events Fatigue, pyrexia, Disrupts sleep, disrupts concentration on daily activities;
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210828; Test Name: Body temperature; Result Unstructured Data: Fever 102 F
- Aktuelle Erkrankungen
- Allergic reaction to analgesics (Allergic to drug Codeine.); Hyperlipidemia; Hypertension; Hypothyroidism; Sulfonamide allergy (Allergic to sulfa antibiotics.); Tinnitus (Mild tinnitus)
- Vorgeschichte
- -
- Andere Medikamente
- HYDROCHLOROTHIAZIDE; LEVOTHYROXINE; ROSUVASTATINE [ROSUVASTATIN]; BENAZEPRIL; AMLODIPINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 14.10.2021
- Impfdatum
- 05.10.2021
- Beginn
- 05.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diplopia
Fatigue
Symptomtext
Double vision, fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin, Gabapentin, Percocet.
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 12.10.2021
- Impfdatum
- 12.08.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anal incontinence
Bladder discomfort
Cardiac discomfort
Headache
Micturition urgency
Pain
Sleep disorder
Somnolence
Urine analysis
Symptomtext
I went home immediately after having the shot and had to sleep for 2 hours. I woke up with a headache. The headache was gone by the next morning. Then, 3 days later I started having fecal incontinence that lasted for approximately 2 weeks. I've also had 4 episodes where my heart felt like someone was squeezing it. Two ofthe episodes happened in the middle of the night and woke me up. Two episodes happened during the afternoon and evening while I was watching TV. After the fecal incontinence subsided I felt like I was getting a UTI because I had pressure and pain that went along with an urgency to urinate. I got on antibiotics, but that didn't help and when I gave a sample, there was no bacteria found. This went on for about 10 days and the pain and pressure finally went away. I was 60 years old when I had the Shingrix shot in June, 2020.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- My urine was checked for bacteria. My doctor has the results. I don't remember the exact date I had the test, but it was around 8/30/21.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Seasonal Allergies, Asthma
- Andere Medikamente
- Allegra
- Allergien
- Cipro, Premarin
- Vorherige Impfungen
- I had a bad reaction to the second Shingrix shot. I felt like I had the flu for 3 days.
- Staat
- AK
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 11.10.2021
- Impfdatum
- 08.10.2021
- Beginn
- 09.10.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Symptomtext
Pt reported red, itchy, hot and swollen area about a 4 inch in diameter area around the injection site starting about 24 hours after receiving the moderna vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- No Known Drug Allergies
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 10.10.2021
- Impfdatum
- 02.10.2021
- Beginn
- 02.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Exercise tolerance decreased
Fatigue
Feeling abnormal
Lymphadenopathy
Pain
Symptomtext
I have been fatigued and achy all over since 6:00 PM on the day I received the shot. It has been eight days. My lymph nodes at my collarbone and under my arm on my left side or swollen. That began the day after, Sunday, October 3. They are currently smaller but still swollen. I still ache all over and I feel terrible. I have tried to stay moderately active. I normally work out six days a week. I have done just three very light workouts this past week, thinking that might help. But it hasn?t. I have drank lots of water and tried to eat right. I am afraid of getting the second shot because I still feel so bad from the first. This is almost as bad as having Covid back in January.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- I had COVID-19 in January 2021. Staph infection in my nose about 6 weeks prior to vaccination.
- Vorgeschichte
- endometriosis which I take the birth control for, and anxiety and depression for which I started taking Prozac beginning September 21, 2021.
- Andere Medikamente
- Microgestin 24 fe once daily Prozac 20 mg once daily
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 09.10.2021
- Impfdatum
- 06.10.2021
- Beginn
- 06.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Injection site erythema
Injection site swelling
Peripheral swelling
Pruritus
Swelling
Symptomtext
Patient presented to the pharmacy on 10/08/21 and expressed concern over her arm following her third Moderna vaccine. She stated that her arm that she received the vaccine in is red, swollen, and itchy. She stated that the redness and swelling had spread from the localized injection site extending down to her elbow. She stated that she had brought this to the attention of her physician at the first occurrence of the redness and swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Neosporin topical
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 07.10.2021
- Impfdatum
- 03.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Arthralgia
Back pain
Chills
Lethargy
Malaise
Nausea
Pain
Vaccination site bruising
Vaccination site haemorrhage
Vaccination site mass
Vaccination site pain
Vaginal haemorrhage
Symptomtext
vaginal bleeding; lethargic; upper and lower back pain/pain in her upper back; didn't feel good; general aches and pains like she had the flu; a little nauseous; pain around her shoulders; chills; injection site was tender to the touch/injection site pain/tender to the touch; injection site was raised/raised bump at the injection site; injection site bruised/bruising around the injection site; bled a lot after the injection; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE MASS (injection site was raised/raised bump at the injection site), VACCINATION SITE BRUISING (injection site bruised/bruising around the injection site), VAGINAL HAEMORRHAGE (vaginal bleeding), LETHARGY (lethargic) and BACK PAIN (upper and lower back pain/pain in her upper back) in a 41-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 03-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Aug-2021, the patient experienced VACCINATION SITE MASS (injection site was raised/raised bump at the injection site), VACCINATION SITE BRUISING (injection site bruised/bruising around the injection site), VACCINATION SITE HAEMORRHAGE (bled a lot after the injection) and VACCINATION SITE PAIN (injection site was tender to the touch/injection site pain/tender to the touch). On 04-Aug-2021, the patient experienced VAGINAL HAEMORRHAGE (vaginal bleeding), LETHARGY (lethargic), BACK PAIN (upper and lower back pain/pain in her upper back), MALAISE (didn't feel good), PAIN (general aches and pains like she had the flu), NAUSEA (a little nauseous), ARTHRALGIA (pain around her shoulders) and CHILLS (chills). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency. On 06-Aug-2021, PAIN (general aches and pains like she had the flu) had resolved. In August 2021, BACK PAIN (upper and lower back pain/pain in her upper back) and ARTHRALGIA (pain around her shoulders) had resolved. At the time of the report, VACCINATION SITE MASS (injection site was raised/raised bump at the injection site), VACCINATION SITE BRUISING (injection site bruised/bruising around the injection site), LETHARGY (lethargic), MALAISE (didn't feel good), VACCINATION SITE HAEMORRHAGE (bled a lot after the injection), NAUSEA (a little nauseous), VACCINATION SITE PAIN (injection site was tender to the touch/injection site pain/tender to the touch) and CHILLS (chills) outcome was unknown and VAGINAL HAEMORRHAGE (vaginal bleeding) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No relevant concomitant medications were reported. Treatment includes Ice and Tea This case was linked to MOD-2021-336033 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 02.10.2021
- Impfdatum
- 26.07.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Burning sensation
Feeling abnormal
Rash
Symptomtext
Brain fog; Bust out in rash all over the body; Rash all over body and was burning; This spontaneous case was reported by a consumer and describes the occurrence of BURNING SENSATION (Rash all over body and was burning), FEELING ABNORMAL (Brain fog) and RASH (Bust out in rash all over the body) in a 60-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 002F21 and 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 26-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 23-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 23-Aug-2021, the patient experienced BURNING SENSATION (Rash all over body and was burning) and RASH (Bust out in rash all over the body). On 24-Aug-2021, the patient experienced FEELING ABNORMAL (Brain fog). In September 2021, FEELING ABNORMAL (Brain fog) had resolved. At the time of the report, BURNING SENSATION (Rash all over body and was burning) and RASH (Bust out in rash all over the body) outcome was unknown. Concomitant medication information was not provided by the reporter. Treatment information was not provided by the reporter. It was reported that the pharmacist recommended to take but patient didn't took it as she did not like drugs. 1 month after bump down arm she got injection in back and so was rash all over body. This case was linked to MOD-2021-329732 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 01.10.2021
- Impfdatum
- 26.07.2021
- Beginn
- 26.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Peripheral swelling
Rash
Symptomtext
Bump in arm; Big red whelp; mild ache in shoulder; This spontaneous case was reported by a consumer and describes the occurrence of PERIPHERAL SWELLING (Bump in arm), RASH (Big red whelp) and ARTHRALGIA (mild ache in shoulder) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 26-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 ARTHRALGIA (mild ache in shoulder). On 16-Aug-2021, the patient experienced PERIPHERAL SWELLING (Bump in arm) and RASH (Big red whelp). At the time of the report, PERIPHERAL SWELLING (Bump in arm), RASH (Big red whelp) and ARTHRALGIA (mild ache in shoulder) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant and treatment information were reported by the reporter This case was linked to MOD-2021-329763 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 01.10.2021
- Impfdatum
- 27.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Headache
Sleep disorder
Vomiting
Symptomtext
Pain in left breast; Pounding heart; Brain fog; Bowel pain; Wakes out of deep sleep; Headache; Vomiting; This spontaneous case was reported by a consumer and describes the occurrence of BREAST PAIN (Pain in left breast), PALPITATIONS (Pounding heart), FEELING ABNORMAL (Brain fog), ABDOMINAL PAIN (Bowel pain) and SLEEP DISORDER (Wakes out of deep sleep) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 062E21A and 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Tumor and Surgical procedure. Concurrent medical conditions included Celiac disease. On 27-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 24-Aug-2021, 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 experienced BREAST PAIN (Pain in left breast), PALPITATIONS (Pounding heart), FEELING ABNORMAL (Brain fog), ABDOMINAL PAIN (Bowel pain), SLEEP DISORDER (Wakes out of deep sleep), HEADACHE (Headache) and VOMITING (Vomiting). At the time of the report, BREAST PAIN (Pain in left breast), PALPITATIONS (Pounding heart), FEELING ABNORMAL (Brain fog), ABDOMINAL PAIN (Bowel pain), SLEEP DISORDER (Wakes out of deep sleep), HEADACHE (Headache) and VOMITING (Vomiting) outcome was unknown. No concomitant treatment was provided. No treatment medication was provided. This case was linked to MOD-2021-329010.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Celiac disease
- Vorgeschichte
- Medical History/Concurrent Conditions: Surgical procedure; Tumor
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 28.09.2021
- Impfdatum
- 05.09.2021
- Beginn
- 07.09.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain in extremity
Peripheral swelling
Skin warm
Symptomtext
redness, pain and warmth on left arm, pain and swelling of left hand
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- rovestatin and vitamins
- Allergien
- Malarone
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 25.09.2021
- Impfdatum
- 17.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination complication
Vaccination site rash
Symptomtext
Slight reaction on the vaccine arm; Rash; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (Slight reaction on the vaccine arm) and VACCINATION SITE RASH (Rash) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No relevant medical history was reported. On 17-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced VACCINATION COMPLICATION (Slight reaction on the vaccine arm) and VACCINATION SITE RASH (Rash). At the time of the report, VACCINATION COMPLICATION (Slight reaction on the vaccine arm) and VACCINATION SITE RASH (Rash) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) dosing remained unchanged. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant information was-thyroid medication , Blood pressure medication ,Lipid medication ,Allergy medication ,cream for the rosacea. No treatment information was provided. This case was linked to MOD-2021-321100 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No relevant medical history was reported.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 24.09.2021
- Impfdatum
- 24.07.2021
- Beginn
- 04.08.2021
- Tage bis Beginn
- 11,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest X-ray
Chills
Cough
Laboratory test
Nasal congestion
Oropharyngeal pain
Pain
Pyrexia
Rhinorrhoea
SARS-CoV-2 test
Symptomtext
Pt came to ER c/o body aches, cough, sore throat, rhinorrhea, nasal congestion, chills, fever. Onset 5 days prior to arrival.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Covid test, cxr, lab work.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 21.09.2021
- Impfdatum
- 16.07.2021
- Beginn
- 16.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Bone pain
Butterfly rash
Chills
Erythema
Feeling hot
Flushing
Headache
Heart rate increased
Insomnia
Nausea
Vomiting
Symptomtext
Nausea/vomiting; Nausea/vomiting; Chills; Head ache; Flushing; Feeling hot; Red face the next day; Pretty significant pain in hip; Pretty significant pain in bone; Heart rate went up; Big, butterfly rash on her face; Hard time sleeping; This spontaneous case was reported by a consumer and describes the occurrence of BONE PAIN (Pretty significant pain in bone), HEART RATE INCREASED (Heart rate went up), BUTTERFLY RASH (Big, butterfly rash on her face), INSOMNIA (Hard time sleeping) and ERYTHEMA (Red face the next day) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Hypersensitivity reaction (NOS) (Hypersensitivity reactions). Previously administered products included for an unreported indication: Flu Vaccine (welts down arm from injection site to wrist (almost in a distribution line) following vein/or nerve gone by day 3.) in 2020. Concurrent medical conditions included Sjogren's (worsened, sores in nose, vertigo, increased pain in joints and bones, increased dryness, and dizziness), Dysautonomia (worsened, sores in nose, vertigo, increased pain in joints and bones, increased dryness, and dizziness) and Autoimmune disorder NOS (Autoimmune disease). Concomitant products included AUTOLOGOUS HUMAN CORNEAL EPITHELIAL CELLS for Dry eyes, HYDROXYCHLOROQUINE, METHOTREXATE, KETOTIFEN from an unknown date to 04-Sep-2021, ESTRADIOL, PANTOPRAZOLE, VITAMINS NOS, CICLOSPORIN (RESTASIS), HYDROXYCHLOROQUINE SULFATE (PLAQUENIL [HYDROXYCHLOROQUINE SULFATE]), NALTREXONE HYDROCHLORIDE (NALTREXON) and TOPIRAMATE for an unknown indication. On 16-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Jul-2021, the patient experienced BONE PAIN (Pretty significant pain in bone), HEART RATE INCREASED (Heart rate went up), BUTTERFLY RASH (Big, butterfly rash on her face), INSOMNIA (Hard time sleeping) and ARTHRALGIA (Pretty significant pain in hip). On 18-Jul-2021, the patient experienced ERYTHEMA (Red face the next day). On an unknown date, the patient experienced FLUSHING (Flushing), FEELING HOT (Feeling hot), NAUSEA (Nausea/vomiting), VOMITING (Nausea/vomiting), CHILLS (Chills) and HEADACHE (Head ache). The patient was treated with KETOROLAC TROMETHAMINE (TORADOL) for Pain, at an unspecified dose and frequency; PREDNISONE at a dose of 5 days and SALINE [SODIUM CHLORIDE] (intravenous) for Adverse event, at an unspecified dose and frequency. At the time of the report, BONE PAIN (Pretty significant pain in bone), HEART RATE INCREASED (Heart rate went up), BUTTERFLY RASH (Big, butterfly rash on her face), INSOMNIA (Hard time sleeping), ERYTHEMA (Red face the next day), FLUSHING (Flushing), FEELING HOT (Feeling hot), ARTHRALGIA (Pretty significant pain in hip), NAUSEA (Nausea/vomiting), VOMITING (Nausea/vomiting), CHILLS (Chills) and HEADACHE (Head ache) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment medications also included unspecified steroids Most recent FOLLOW-UP information incorporated above includes: On 10-Sep-2021: FU received on 13-SEP-2021 include second dose information, patient demographics updated, concomitant medications added, treatment information updated, onset date for events (bone pain, arthralgia, insomnia, butterfly rash and heart rate increased) updated, current condition Autoimmune disease and historical condition hypersensitivity reactions updated, concomitant medication information updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Autoimmune disorder NOS (Autoimmune disease); Sjogren's (worsened, sores in nose, vertigo, increased pain in joints and bones, increased dryness, and dizziness)
- Vorgeschichte
- Medical History/Concurrent Conditions: Dysautonomia (worsened, sores in nose, vertigo, increased pain in joints and bones, increased dryness, and dizziness); Hypersensitivity reaction (NOS) (Hypersensitivity reactions)
- Andere Medikamente
- HYDROXYCHLOROQUINE; METHOTREXATE; KETOTIFEN; ESTRADIOL; PANTOPRAZOLE; VITAMINS NOS; RESTASIS; AUTOLOGOUS HUMAN CORNEAL EPITHELIAL CELLS; PLAQUENIL [HYDROXYCHLOROQUINE SULFATE]; NALTREXON; TOPIRAMATE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 20.09.2021
- Impfdatum
- 18.09.2021
- Beginn
- 20.09.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Interchange of vaccine products
Symptomtext
Patient was given a mixed series of the COVID vaccine. He did not experience any signs or symptoms of adverse reactions from the mixed series aside from a sore arm of the injection site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 20.09.2021
- Impfdatum
- 12.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Vaccine positive rechallenge
Symptomtext
Severe headaches after shot, both 1st and second shots, I never had headaches like this before? slowly disappearing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Ramipril
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 18.09.2021
- Impfdatum
- 22.01.2021
- Beginn
- 01.01.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Lymphadenopathy
Nausea
Product dose omission issue
Vaccination complication
Symptomtext
She did get a little nauseated; she had a reaction; She tried to receive the second dose today, but the pharmacy turned her away; A week after the first dose, swollen lymph node under my armpit/lymph node stayed about 3 weeks; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (she had a reaction), NAUSEA (She did get a little nauseated), LYMPHADENOPATHY (A week after the first dose, swollen lymph node under my armpit/lymph node stayed about 3 weeks) and PRODUCT DOSE OMISSION ISSUE (She tried to receive the second dose today, but the pharmacy turned her away) in a 62-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 22-Jan-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In January 2021, the patient experienced LYMPHADENOPATHY (A week after the first dose, swollen lymph node under my armpit/lymph node stayed about 3 weeks). On 27-Aug-2021, the patient experienced VACCINATION COMPLICATION (she had a reaction) and PRODUCT DOSE OMISSION ISSUE (She tried to receive the second dose today, but the pharmacy turned her away). On an unknown date, the patient experienced NAUSEA (She did get a little nauseated). In February 2021, LYMPHADENOPATHY (A week after the first dose, swollen lymph node under my armpit/lymph node stayed about 3 weeks) had resolved. On 27-Aug-2021, PRODUCT DOSE OMISSION ISSUE (She tried to receive the second dose today, but the pharmacy turned her away) had resolved. At the time of the report, VACCINATION COMPLICATION (she had a reaction) and NAUSEA (She did get a little nauseated) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medication was reported. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 18.09.2021
- Impfdatum
- 17.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site pain
Symptomtext
She had a sore arm; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (She had a sore arm) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D2-1A) for COVID-19 vaccination. The patient's past medical history included Breast cancer. Concomitant products included MONTELUKAST SODIUM (SINGULAIR) for an unknown indication. On 17-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced VACCINATION SITE PAIN (She had a sore arm). At the time of the report, VACCINATION SITE PAIN (She had a sore arm) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Reported stated she received vaccine in the left arm as her doctor stated not to do it on her right arm because of breast cancer. No Treatment medications provided. This case was linked to MOD-2021-287461 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Breast cancer
- Andere Medikamente
- SINGULAIR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 28.08.2021
- Beginn
- 28.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Erythema
Hypersensitivity
Lymphadenopathy
Pharyngeal swelling
Pyrexia
Rash
Vaccination site swelling
Varicella
Symptomtext
Throat swelled; An allergic Reaction; Red arm; Hot to touch; Chickenpox scares became inflamed and red; Rash all over body; Injection site swelled; Lymph nodes in the neck also swelled; Fever; This spontaneous case was reported by an other health care professional and describes the occurrence of PHARYNGEAL SWELLING (Throat swelled), HYPERSENSITIVITY (An allergic Reaction), ERYTHEMA (Red arm), BURNING SENSATION (Hot to touch) and VARICELLA (Chickenpox scares became inflamed and red) in a 38-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 28-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 28-Aug-2021, the patient experienced PHARYNGEAL SWELLING (Throat swelled), HYPERSENSITIVITY (An allergic Reaction), ERYTHEMA (Red arm), BURNING SENSATION (Hot to touch), VARICELLA (Chickenpox scares became inflamed and red), RASH (Rash all over body), VACCINATION SITE SWELLING (Injection site swelled), LYMPHADENOPATHY (Lymph nodes in the neck also swelled) and PYREXIA (Fever). The patient was treated with DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) for Adverse event, at an unspecified dose and frequency; PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency; IBUPROFEN for Adverse event, at an unspecified dose and frequency and CORTISONE for Adverse event, at an unspecified dose and frequency. At the time of the report, PHARYNGEAL SWELLING (Throat swelled), HYPERSENSITIVITY (An allergic Reaction), ERYTHEMA (Red arm), BURNING SENSATION (Hot to touch), VARICELLA (Chickenpox scares became inflamed and red), RASH (Rash all over body), VACCINATION SITE SWELLING (Injection site swelled), LYMPHADENOPATHY (Lymph nodes in the neck also swelled) and PYREXIA (Fever) 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. Concomitant medications details were not reported by the reporter. Treatment also included prescribed steroids. Reporter stated that patient currently taking other medications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- -
- Geschlecht
- F
- Eingang
- 13.09.2021
- Impfdatum
- 05.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Balance disorder
Dizziness
Headache
Malaise
Myalgia
Nausea
Pain in extremity
Pyrexia
Vaccination site erythema
Symptomtext
Felt sick; Arm hurts; Off balance; Lightheaded; Run a fever on and off; Headache; Body aches muscle aches; Nauseas if I eat something I feel like I'm going to throw up; Redness in the injection site; This spontaneous case was reported by a consumer and describes the occurrence of MALAISE (Felt sick), PAIN IN EXTREMITY (Arm hurts), BALANCE DISORDER (Off balance), DIZZINESS (Lightheaded) and PYREXIA (Run a fever on and off) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 062E21A and 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 05-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 31-Aug-2021, 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 experienced MALAISE (Felt sick), PAIN IN EXTREMITY (Arm hurts), BALANCE DISORDER (Off balance), DIZZINESS (Lightheaded), PYREXIA (Run a fever on and off), HEADACHE (Headache), MYALGIA (Body aches muscle aches), NAUSEA (Nauseas if I eat something I feel like I'm going to throw up) and VACCINATION SITE ERYTHEMA (Redness in the injection site). At the time of the report, MALAISE (Felt sick), PAIN IN EXTREMITY (Arm hurts), BALANCE DISORDER (Off balance), DIZZINESS (Lightheaded), PYREXIA (Run a fever on and off), HEADACHE (Headache), MYALGIA (Body aches muscle aches), NAUSEA (Nauseas if I eat something I feel like I'm going to throw up) and VACCINATION SITE ERYTHEMA (Redness in the injection site) outcome was unknown. Concomitant medication included Medication for diabetes type 2. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 13.09.2021
- Impfdatum
- 03.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Back pain
Burning sensation
Hypoaesthesia
Influenza like illness
Insomnia
Neck pain
Neuralgia
Pain
Pain in extremity
Symptomtext
middle of the night and there was pain on the left side, pain that was throbbing and excruciating nerve pain that lasted for 2 weeks; could not fall asleep; developing pain in the neck area; developing pain in upper back area; pain was radiating down on to his arm that he received the injection; excruciating nerve pain that lasted for 2 weeks; developed flu like symptoms; still have patches of skin on forearm that feel numb; Patient also noticed patches of skin on his hand and forearm that felt burning; developing pain in shoulder area, 30 days later have paralysis pain in his shoulder with 0 control/movement in the shoulder; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (middle of the night and there was pain on the left side, pain that was throbbing and excruciating nerve pain that lasted for 2 weeks), INSOMNIA (could not fall asleep), NECK PAIN (developing pain in the neck area), BACK PAIN (developing pain in upper back area) and PAIN IN EXTREMITY (pain was radiating down on to his arm that he received the injection) in a 34-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No medical history was provided by the reporter. On 03-Aug-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced PAIN (middle of the night and there was pain on the left side, pain that was throbbing and excruciating nerve pain that lasted for 2 weeks), INSOMNIA (could not fall asleep), NECK PAIN (developing pain in the neck area), BACK PAIN (developing pain in upper back area), PAIN IN EXTREMITY (pain was radiating down on to his arm that he received the injection), NEURALGIA (excruciating nerve pain that lasted for 2 weeks), INFLUENZA LIKE ILLNESS (developed flu like symptoms), HYPOAESTHESIA (still have patches of skin on forearm that feel numb), BURNING SENSATION (Patient also noticed patches of skin on his hand and forearm that felt burning) and ARTHRALGIA (developing pain in shoulder area, 30 days later have paralysis pain in his shoulder with 0 control/movement in the shoulder). The patient was treated with OXYCODONE for Pain, at an unspecified dose and frequency and GABAPENTIN for Pain, at an unspecified dose and frequency. At the time of the report, PAIN (middle of the night and there was pain on the left side, pain that was throbbing and excruciating nerve pain that lasted for 2 weeks), INSOMNIA (could not fall asleep), NECK PAIN (developing pain in the neck area), BACK PAIN (developing pain in upper back area), PAIN IN EXTREMITY (pain was radiating down on to his arm that he received the injection), NEURALGIA (excruciating nerve pain that lasted for 2 weeks), INFLUENZA LIKE ILLNESS (developed flu like symptoms), HYPOAESTHESIA (still have patches of skin on forearm that feel numb), BURNING SENSATION (Patient also noticed patches of skin on his hand and forearm that felt burning) and ARTHRALGIA (developing pain in shoulder area, 30 days later have paralysis pain in his shoulder with 0 control/movement in the shoulder) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were reported. It was reported Patient had seen his primary care physician about the adverse event and was advice not to take the 2nd dose of the Moderna COVID-19 vaccine and was advised to see a neurologist although patient was not able to to see a Neurologist because the office requires patients to be full-vaccinated if not Neurologist will see them through telehealth.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 08.09.2021
- Impfdatum
- 16.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Headache
Pain in extremity
Symptomtext
chills; fatigue; headache; pain in the arm; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (pain in the arm), CHILLS (chills), FATIGUE (fatigue) and HEADACHE (headache) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) 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 an unknown date, the patient experienced PAIN IN EXTREMITY (pain in the arm), CHILLS (chills), FATIGUE (fatigue) and HEADACHE (headache). At the time of the report, PAIN IN EXTREMITY (pain in the arm) had resolved and CHILLS (chills), FATIGUE (fatigue) and HEADACHE (headache) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No relevant concomitant medications were reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 12.08.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood urine present
Diarrhoea
Fatigue
Pyrexia
Symptomtext
Fever, fatigue, blood in urine, diarrhea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 23.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 9,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pruritus
Injection site swelling
Rash
Symptomtext
Site: Itching at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Rash Generalized-Mild, Additional Details: PATIENT HAS STATED RASH SPREADS FROM EXTREMITIES UP TO THE COLLARBONE. PHARMACY HAS ADVISED TO TAKE BENADRYL, PATIENT HAS ONLY TRIED CETIRIZINE FOR THE LAST COUPLE OF DAYS. REACTION DID NOT START UNTIL A WEEK AFTE VACCINATION DATE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 23.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Symptomtext
headache nonstop; This spontaneous case was reported by a consumer and describes the occurrence of HEADACHE (headache nonstop) in a 45-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 23-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 23-Jul-2021, the patient experienced HEADACHE (headache nonstop). The patient was treated with PARACETAMOL (TYLENOL) for Headache, at an unspecified dose and frequency and IBUPROFEN (ADVIL [IBUPROFEN]) for Headache, at an unspecified dose and frequency. At the time of the report, HEADACHE (headache nonstop) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No Concomitant medication information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 22.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Pain in extremity
Symptomtext
Sore arm; Feeling tired; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Sore arm) and FATIGUE (Feeling tired) in a 33-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. Medical history was not provided by reporter. Concomitant products included MULTIVITAMINS [VITAMINS NOS], VITAMIN C [ASCORBIC ACID], VITAMIN D NOS and SIMVASTATIN for an unknown indication. On 22-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced PAIN IN EXTREMITY (Sore arm) and FATIGUE (Feeling tired). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at an unspecified dose and frequency. At the time of the report, PAIN IN EXTREMITY (Sore arm) and FATIGUE (Feeling tired) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment medication also included hydrate. This case was linked to MOD-2021-293366 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: Medical history was not provided by reporter.
- Andere Medikamente
- MULTIVITAMINS [VITAMINS NOS]; VITAMIN C [ASCORBIC ACID]; VITAMIN D NOS; SIMVASTATIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 04.09.2021
- Impfdatum
- 10.08.2021
- Beginn
- 10.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cold sweat
Eye disorder
Headache
Hyperhidrosis
Magnetic resonance imaging
Myalgia
Vision blurred
Visual field defect
Symptomtext
sweaty; clammy; blurred vision; His left eye had no peripheral vision; it was like he had spider webs in both eyes; headache; left chest muscle was sore and kind of hurt; This spontaneous case was reported by a consumer and describes the occurrence of HYPERHIDROSIS (sweaty), COLD SWEAT (clammy), VISION BLURRED (blurred vision), VISUAL FIELD DEFECT (His left eye had no peripheral vision) and EYE DISORDER (it was like he had spider webs in both eyes) in a 58-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No relevant medical history was reported. Concomitant products included DOXYCYCLINE and MULTIVITAMINS [VITAMINS NOS] for an unknown indication. On 10-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Aug-2021, the patient experienced HEADACHE (headache) and MYALGIA (left chest muscle was sore and kind of hurt). On 11-Aug-2021, the patient experienced HYPERHIDROSIS (sweaty), COLD SWEAT (clammy), VISION BLURRED (blurred vision), VISUAL FIELD DEFECT (His left eye had no peripheral vision) and EYE DISORDER (it was like he had spider webs in both eyes). The patient was treated with PARACETAMOL (TYLENOL) for Adverse event, at a dose of 1 dosage form. At the time of the report, HYPERHIDROSIS (sweaty), COLD SWEAT (clammy), HEADACHE (headache) and MYALGIA (left chest muscle was sore and kind of hurt) outcome was unknown and VISION BLURRED (blurred vision), VISUAL FIELD DEFECT (His left eye had no peripheral vision) and EYE DISORDER (it was like he had spider webs in both eyes) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Magnetic resonance imaging: normal (normal) found no tumor, brain bleed, stroke, neurological, or cardiac disorder.. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient also had an ekg and blood draw and spent about 7 hours in the ER. The emergency room doctor did say that when multiple sclerosis affects vision it lasts for days or weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- Test Name: MRI; Result Unstructured Data: found no tumor, brain bleed, stroke, neurological, or cardiac disorder.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No relevant medical history was reported.
- Andere Medikamente
- MULTIVITAMINS [VITAMINS NOS]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 04.09.2021
- Impfdatum
- 03.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia
Pain in jaw
Sinus pain
Symptomtext
Her jaw hurt for 3 days; Her sinuses hurt for 3 days; The left side of her neck numbed up/ the left side of her face numbed up; This spontaneous case was reported by a consumer and describes the occurrence of HYPOAESTHESIA (The left side of her neck numbed up/ the left side of her face numbed up), PAIN IN JAW (Her jaw hurt for 3 days) and SINUS PAIN (Her sinuses hurt for 3 days) in a 39-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Aug-2021, the patient experienced HYPOAESTHESIA (The left side of her neck numbed up/ the left side of her face numbed up). On 04-Aug-2021, the patient experienced PAIN IN JAW (Her jaw hurt for 3 days) and SINUS PAIN (Her sinuses hurt for 3 days). On 04-Aug-2021, HYPOAESTHESIA (The left side of her neck numbed up/ the left side of her face numbed up) had resolved. In August 2021, PAIN IN JAW (Her jaw hurt for 3 days) and SINUS PAIN (Her sinuses hurt for 3 days) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant product use was provided by the reporter. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in jaw
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 01.09.2021
- Impfdatum
- 01.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Symptomtext
Patient developed a bruise at injection site. The site was on the lower left arm, not on the deltoid muscle. The bruise was still there when she came back in for her second dose on 8/29/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 31.08.2021
- Impfdatum
- 28.08.2021
- Beginn
- 28.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Inflammation
Lymph node pain
Pharyngeal swelling
Pyrexia
Rash
Skin warm
Swelling
Symptomtext
High feaver, swelling is the left arm sore and hot lymph nodes and throat swelled shut rash and feaver chicken pox scares became red and inflamed lasting over 72 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymph node pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 30.08.2021
- Impfdatum
- 28.08.2021
- Beginn
- 28.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Headache
Pain
Pyrexia
Urinary incontinence
Symptomtext
Fever, body aches, back aches, severe headaches, uncontrollable urinations, took Tylenol.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Osteoporosis.
- Andere Medikamente
- Vitamins.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 29.08.2021
- Impfdatum
- 01.08.2021
- Beginn
- 27.08.2021
- Tage bis Beginn
- 26,0
- Dosis
- 1
- Route/Site
- UN / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Induration
Injection site erythema
Injection site pain
Injection site swelling
Pain
Skin warm
Symptomtext
Firmness, extreme soreness, painful muscles at injection site, redness, swelling at injection site, warm/hot to touch. Started about 10 minutes after the vaccine, but since none of these symptoms were mentioned, I believed they were normal. First dose was the same and lasted about a week - a week and a half
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- Should I go to the doctors?!!!!
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Carpal tunnel Dermatographia Seasonal allergies
- Andere Medikamente
- -
- Allergien
- Antibiotics (penicillin, amoxicillin) Bleach Coconut Chocolate Ginger Banana
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 19.07.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 28,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Ear discomfort
Eye pain
Headache
Hypoacusis
Lymphadenopathy
Myalgia
Neck pain
Pyrexia
Vaccination site erythema
Vaccination site pruritus
Vaccination site swelling
Symptomtext
Pain in the Head, Neck and Shoulder (Where the neck connects to the shoulder) after the second shot; Eye balls hurt after the second shot; Left ear clogged up after the second shot; Could not hear in the left ear after the second shot; Itching Injection Site on the left arm after the second shot; Headache after the second shot, Pain in the Head; Low Grade Fever 99.7F after the second shot; Hurt all over her body after the second shot; Chills after the second shot after the second shot; Swollen gland on the left side of the neck after the second shot; Red Injection Site on the left arm after the second shot; Swollen Injection Site on the left arm after the second shot; Shoulder pain; This spontaneous case was reported by a consumer and describes the occurrence of NECK PAIN (Pain in the Head, Neck and Shoulder (Where the neck connects to the shoulder) after the second shot), EYE PAIN (Eye balls hurt after the second shot), EAR DISCOMFORT (Left ear clogged up after the second shot), HYPOACUSIS (Could not hear in the left ear after the second shot) and VACCINATION SITE PRURITUS (Itching Injection Site on the left arm after the second shot) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 091D21A and 088C21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 19-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 16-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 16-Aug-2021, the patient experienced NECK PAIN (Pain in the Head, Neck and Shoulder (Where the neck connects to the shoulder) after the second shot), EYE PAIN (Eye balls hurt after the second shot), EAR DISCOMFORT (Left ear clogged up after the second shot), HYPOACUSIS (Could not hear in the left ear after the second shot), VACCINATION SITE PRURITUS (Itching Injection Site on the left arm after the second shot), HEADACHE (Headache after the second shot, Pain in the Head), PYREXIA (Low Grade Fever 99.7F after the second shot), MYALGIA (Hurt all over her body after the second shot), CHILLS (Chills after the second shot after the second shot), LYMPHADENOPATHY (Swollen gland on the left side of the neck after the second shot), VACCINATION SITE ERYTHEMA (Red Injection Site on the left arm after the second shot), VACCINATION SITE SWELLING (Swollen Injection Site on the left arm after the second shot) and ARTHRALGIA (Shoulder pain). At the time of the report, NECK PAIN (Pain in the Head, Neck and Shoulder (Where the neck connects to the shoulder) after the second shot), EYE PAIN (Eye balls hurt after the second shot), EAR DISCOMFORT (Left ear clogged up after the second shot), HYPOACUSIS (Could not hear in the left ear after the second shot), VACCINATION SITE PRURITUS (Itching Injection Site on the left arm after the second shot), HEADACHE (Headache after the second shot, Pain in the Head), PYREXIA (Low Grade Fever 99.7F after the second shot), MYALGIA (Hurt all over her body after the second shot), CHILLS (Chills after the second shot after the second shot), LYMPHADENOPATHY (Swollen gland on the left side of the neck after the second shot), VACCINATION SITE ERYTHEMA (Red Injection Site on the left arm after the second shot), VACCINATION SITE SWELLING (Swollen Injection Site on the left arm after the second shot) and ARTHRALGIA (Shoulder pain) outcome was unknown. No concomitant medications were provided by the reporter. No treatment information was provided by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2021-291138 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2021-291138:wife case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- -
- Geschlecht
- M
- Eingang
- 28.08.2021
- Impfdatum
- 30.07.2021
- Beginn
- 09.08.2021
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Tenderness
Urticaria
Symptomtext
Popping up on feet, like blisters with no fluid; Tender and sore; Welts on hands and feet; This spontaneous case was reported by a consumer and describes the occurrence of URTICARIA (Welts on hands and feet), BLISTER (Popping up on feet, like blisters with no fluid) and TENDERNESS (Tender and sore) in a 27-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 30-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 09-Aug-2021, the patient experienced URTICARIA (Welts on hands and feet). On an unknown date, the patient experienced BLISTER (Popping up on feet, like blisters with no fluid) and TENDERNESS (Tender and sore). At the time of the report, URTICARIA (Welts on hands and feet), BLISTER (Popping up on feet, like blisters with no fluid) and TENDERNESS (Tender and sore) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Concomitant medications were not provided. Treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 09.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature
Chills
Feeling cold
Headache
Night sweats
Pyrexia
Rash erythematous
Skin warm
Vaccination complication
Symptomtext
Felt under the weather; Reaction started left arm that was hot to the touch on arm; Red, splotchy in circle patterns (started out fairly small and are now 2 inches in length); Surrounding area where splotches are not, are cold to touch; Night sweats; Fever, it was pretty intense/ I still feel like I have a low grade fever; Chills; Headache; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION COMPLICATION (Felt under the weather), SKIN WARM (Reaction started left arm that was hot to the touch on arm), RASH ERYTHEMATOUS (Red, splotchy in circle patterns (started out fairly small and are now 2 inches in length)), FEELING COLD (Surrounding area where splotches are not, are cold to touch) and NIGHT SWEATS (Night sweats) in a 25-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 88221S and 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 09-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) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced VACCINATION COMPLICATION (Felt under the weather), SKIN WARM (Reaction started left arm that was hot to the touch on arm), RASH ERYTHEMATOUS (Red, splotchy in circle patterns (started out fairly small and are now 2 inches in length)), FEELING COLD (Surrounding area where splotches are not, are cold to touch), NIGHT SWEATS (Night sweats), PYREXIA (Fever, it was pretty intense/ I still feel like I have a low grade fever), CHILLS (Chills) and HEADACHE (Headache). The patient was treated with PARACETAMOL (TYLENOL) on 08-Aug-2021 for Fever, at an unspecified dose and frequency and IBUPROFEN on 08-Aug-2021 for Pain, at an unspecified dose and frequency. At the time of the report, VACCINATION COMPLICATION (Felt under the weather), SKIN WARM (Reaction started left arm that was hot to the touch on arm), RASH ERYTHEMATOUS (Red, splotchy in circle patterns (started out fairly small and are now 2 inches in length)), FEELING COLD (Surrounding area where splotches are not, are cold to touch), NIGHT SWEATS (Night sweats), CHILLS (Chills) and HEADACHE (Headache) outcome was unknown and PYREXIA (Fever, it was pretty intense/ I still feel like I have a low grade fever) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature: 99.6 degrees fahrenheit (High) 99.6 degrees Fahrenheit. Patient's concomitant medications were reported as none, though she takes Tylenol and ibuprofen as needed for unassociated pain and swelling throughout normal life pattern. Onset date of events was reported as an unspecified date in Aug-2021. Action taken with mRNA-1273 in response to the events was not applicable. This case was linked to MOD-2021-283124 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Test Name: body temperature; Result Unstructured Data: 99.6 degrees Fahrenheit
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 24.08.2021
- Impfdatum
- 20.08.2021
- Beginn
- 22.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Pain
Symptomtext
Severe headache - stabbing pain. It lasted about 36 hours. I also had body aches for about 72 hours. Advil helped some.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No acute illness
- Vorgeschichte
- High blood pressure, depression, anxiety, acid reflux, postural orthostatic hypertension, fibromyalgia
- Andere Medikamente
- Zoloft, Wellbutrin, Losartin, Metoprolol, Protonix
- Allergien
- NKA
- Vorherige Impfungen
- Headache with Moderna shot 1 - not as severe and it only lasted about 8 hours that time
- Staat
- MO
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 23.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Dry mouth
Fatigue
Headache
Nausea
Symptomtext
Nausea Headache Dizzy Dry Mouth Fatigue
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Rheumatoid Arthritis Fibromyalgia Chronic Kidney Disease GERD Chronic UTI
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 23.08.2021
- Impfdatum
- 22.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal discomfort
Blood sodium
Chills
Injection site bruising
Nausea
Pain
Pyrexia
Symptomtext
Severe fever of 101, with Ibuprofen and Tyenol. Body Aches , bruising at injection sight Nausea and upset stomach Body chills
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Na
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- ibuprofen and Tylenol
- Allergien
- Nickel
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 19.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Feeling hot
Pruritus
Skin mass
Symptomtext
Red/Hot area & extreme itching for 1 week 2 days so far. Lump under skin has increased in size x's 3. Never had severe pain with moving arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Multi Vitamin, Calcium, Vitamin B, Vitamin C, Vitamin D, Omega/CQ10 & Red Yeast Rice
- Allergien
- Sulphur Drugs
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 19.08.2021
- Impfdatum
- 11.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site rash
Symptomtext
Developed sore arm on 8th day after shot around injection site and 2 rashes have developed at shot site and and below shot site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- 150MG Sertraline HCL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 18.08.2021
- Impfdatum
- 16.07.2021
- Beginn
- 17.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood magnesium normal
Blood thyroid stimulating hormone normal
Bordetella test positive
Fatigue
Feeling abnormal
Full blood count normal
Headache
Metabolic function test
Vitamin B12
Vitamin D
Symptomtext
Following day of administration, patient developed headaches, brain fog, and fatigue. Symptoms have persisted 1 month following administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Heavy Metals, Lyme Antibody, Lyme Western Blot, CBC, CMP, Magnesium, Vitamin B12, Vitamin D, Folatre, TSH-- within normal limits
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- Asthma, COPD, Osteoporosis, Allergic Rhinitis
- Andere Medikamente
- Zyrtec Singulair Ventolin Flonase Symbicort Zoledronic Acid
- Allergien
- Mold Grass Trees Animal Dander
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 16.08.2021
- Impfdatum
- 08.08.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Rash
Swelling
Symptomtext
The patient started to see a rash and some swelling on Sunday 08/15 in the morning about 7 days after the vaccine, reported the reaction, reports today that the reaction swelling has decreased as well as the redness in color but the size has increased a little.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- UKN
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 16.08.2021
- Impfdatum
- 15.08.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Hyperhidrosis
Product administered to patient of inappropriate age
Symptomtext
Patient was provided a moderna covid 19 vaccination in error. Patient is 16 years of age. Mother was present at time of vaccination. Mother informed immunizer that patient has a history of fainting after vaccinations. Patient was observed for 30 minutes after vaccination. patient experienced dizziness and became sweaty. Patient was provided water and was eased to floor to lay on her back. Patient did not loose consciousness. Patient was monitored and was determined to have recovered from dizziness episode and walked with mother to car to be driven home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- NKA
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 16.08.2021
- Impfdatum
- 07.08.2021
- Beginn
- 15.08.2021
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Injection site rash
Symptomtext
Pt experienced a rash and extreme soreness around injection site. Size of a quarter
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- ill 2 weeks prior w/ body aches for 24 hrs.
- Vorgeschichte
- chronic low back pain/neck
- Andere Medikamente
- Suboxone, advil
- Allergien
- codeine, chocolate, inapsine, beta blockers
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 13.08.2021
- Impfdatum
- 24.07.2021
- Beginn
- 02.08.2021
- Tage bis Beginn
- 9,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chromaturia
Fatigue
Feeling abnormal
Gout
Tinnitus
Symptomtext
Tinnitus, darkened urine, gout, fatigue, brain fog.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- High cholesterol
- Andere Medikamente
- Praluent, Slow FE Iron supplement
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 11.08.2021
- Impfdatum
- 02.08.2021
- Beginn
- 02.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Feeling abnormal
Malaise
Mental impairment
Symptomtext
Patient states that he felt super sick and lightheaded "(could not complete a thought)" for a couple hours after the shot. He also felt very spaced out and "drugged" He called me today to report that he still felt mild lightheadedness and spaciness even after 10 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Patient stated that he had been in a car accident weeks before.
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 11.08.2021
- Impfdatum
- 01.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- MAKING APPT WITH DOCTOR
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- PENICILLINS AND CLEOCIN
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 10.08.2021
- Impfdatum
- 07.08.2021
- Beginn
- 08.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pain in extremity
Rash
Symptomtext
patient reports symptoms of a growing rash in his arm (patient states rash is currently 2x2 inches as of now 8/10). also reports increasing pain. patient had 2nd dose of the moderna on 8/7/21 and reports complaint to pharmacy on 8/10/21. patient directed to call primary care physician.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- glycopyrrolate
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 10.08.2021
- Impfdatum
- 03.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hyperhidrosis
Myalgia
Symptomtext
Burning in my left forearm 15 minutes after injection. The next day the burning spread through out my body. 3 days after the injection excessive sweating. The burning is muscular.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myalgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- Sulfa, NSAIDS, Milk
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 10.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- 05.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Diarrhoea
Fatigue
Injection site erythema
Lethargy
Nausea
Pyrexia
Rash
Urticaria
Symptomtext
Site: Redness at Injection Site-Mild, Systemic: Allergic: Rash Generalized-Medium, Systemic: Diarrhea-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Medium, Systemic: Nausea-Medium, Additional Details: Patient received shot on thursday and had fever, nausea, and diarrhea. On sunday he noticed a rash coming up all over his body. no problems breathing. went to dr today and told him it was hives. he received steroid pack to help and dr recommened 2nd shot while taking steroid
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 06.08.2021
- Impfdatum
- 29.07.2021
- Beginn
- 05.08.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Symptomtext
Left arm at injection sure became red, swollen, and painful a week after receiving the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Birth control
- Allergien
- Sulfa
- Vorherige Impfungen
- Tdap injection infection was treated with antibiotics.
- Staat
- -
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 06.08.2021
- Impfdatum
- 28.07.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash pruritic
Symptomtext
ITY RASH FORMED 3 DAYS AFTER VACCINATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash pruritic
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 05.08.2021
- Impfdatum
- 05.08.2021
- Beginn
- 05.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood pressure increased
Dizziness
Nervousness
Symptomtext
Felt dizzy and shaky with in 3 mins after injection, used automatic blood pressure cuff at the store with help of pharmacy staff BLOOD PRESSURE WAS ELEVATED 225/112
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Rechecked blood pressure over a couple hours continue to be elevated I went to urgent care at my family practice and blood pressure was 190/98 the Dr gave me clonidine and my blood pressure lowered, this was on 8/5/21
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 04.08.2021
- 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: ja
Erholt: nein
Balance disorder
Blood test
Dizziness
Laboratory test normal
Paranasal sinus discomfort
Sinusitis
Urine analysis
Vertigo
Symptomtext
Dizziness, spinning, off balance, and sinus pressure. The dizziness and spinning started less than 24 hours after the vaccine and I still have it 6 days later. Did a visit on Sunday the 8/1/21 and they prescribed me a medicine for dizziness. I also went to the doctors again on 8/3/21 for all the systems. They stated I had vertigo and now the beginnings of sinus infection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- blood tests for infection and urine samples. labs were all normal.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- graves and psoriasis
- Andere Medikamente
- lisinopril, Toprol, Hydrochloridazide, tremfya
- Allergien
- avolox
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 04.08.2021
- Impfdatum
- 14.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Cellulitis
Injection site erythema
Injection site warmth
Symptomtext
Patient reported to the pharmacy on 7/29/21 with a large red circle around injection site that was warm to the touch. Patient reported that the circle had been there since she received the vaccine and had progressively getting larger and worse. I recommended patient present to ER for suspected cellulitis. Patient returned to pharmacy later the same day with antibiotic prescription after ER confirmed cellulitis. Patient received antibiotic and seems to be healing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Phentermine, citalopram, vitamin d, buspirone
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 03.08.2021
- Impfdatum
- 02.08.2021
- Beginn
- 02.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Hypoaesthesia
Vision blurred
Symptomtext
Patient went to urgent care reporting symptoms of numb feet, light headedness/being dizzy, and blurry vision after receiving the covid-19 Moderna vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Strep throat
- Vorgeschichte
- HIV infection
- Andere Medikamente
- Bupropion XL 150mg, Biktarvy
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 02.08.2021
- 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: ja
Chills
Hyperhidrosis
Injection site erythema
Malaise
Pain
Symptomtext
body aches and sores, chills, sweats, covid related symptoms, redness of arm at injection site, for 24 to 36 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- Levocetirizne, lexapro, Aurovela Fe
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 29.07.2021
- Impfdatum
- 22.07.2021
- Beginn
- 29.07.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site reaction
Muscle spasms
Muscle tightness
Symptomtext
Muscle tightness cramping at injection site a week later
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Eosinophilic Asthma
- Andere Medikamente
- -
- Allergien
- Sulfa, Amoxicillin, Clindamycin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 28.07.2021
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Headache
Pruritus
Pustule
Symptomtext
Headache Itching all over body & head Small pustules on right arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 27.07.2021
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Dizziness
Headache
Hypoaesthesia
Symptomtext
Patient started to feel dizzy and light-headed about 10 minutes after vaccine. Gave patient some water and cool compress and monitored patient for about 30 minutes. Patient also started to having tight/numbing feeling in her left hand. Then developed a headache with a tight feeling in her face. Patient started to feel better but was still experiencing effects. Directed patient to seek medical care at urgent care or emergency room.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- hypothyroidism
- Andere Medikamente
- Synthroid 88 mcg
- Allergien
- adhesive
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 27.07.2021
- Impfdatum
- 26.07.2021
- Beginn
- 26.07.2021
- 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
Vision blurred
Vomiting
Symptomtext
Patient received his first dose of the Moderna Covid vaccine and was advised to wait for 15 minutes after the vaccine for monitoring. Immediately after the vaccine, patient reported feeling light headed and blurred vision. He also stated afterwards that he had previously fainted after a blood draw. A certified pharmacy technician administered the vaccine and immediately notified the pharmacist once patient reported symptoms. Patient was given a bottle of water and instructed to remain seated and take deep breaths. He refused offer to call an ambulance. After about 5-7 minutes, patient reported feeling nauseous and vomited. Immediately after vomiting he reported feeling much better. He was instructed to remain seated and stay for observation for another 15 minutes. Patient remained stable and stated he was okay to leave. Followed up with patient in an hour and he reported feeling just fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 26.07.2021
- Impfdatum
- 26.07.2021
- Beginn
- 26.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Flushing
Hyperhidrosis
Symptomtext
patient felt lightheaded, dizzy, flush, sweating - after sitting and drinking some water over 20 minutes pt began to feel better
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 26.07.2021
- Impfdatum
- 25.07.2021
- Beginn
- 25.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysphagia
Pruritus
Symptomtext
10 minutes post vaccination patient reported that he was having some difficulty swallowing and some itching, no other issues. Called 911 and monitored patient until EMS arrived. By the time they arrived he was feeling better and all vitals checked out ok. Patient refused further treatment. Offered Benadryl to patient but he refused. Advised him to take one when he gets home. Followed up with the patient 2 times and he has fully recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- see above
- Aktuelle Erkrankungen
- Not known
- Vorgeschichte
- High blood pressure, high cholesterol, mild anxiety
- Andere Medikamente
- Alprazolam 0.5mg Escitalopram 10mg Lisinopril 10mg Simvastatin 10mg
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 24.07.2021
- Impfdatum
- 24.07.2021
- Beginn
- 24.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Immediate post-injection reaction
Nausea
Symptomtext
She was immediately nauseated, dizzy and lightheaded.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Blood pressure was 171/94 pulse 112, 159/108; pulse 120, 149/113; pulse 121, 174/109; pulse 121, 135/100; pulse 120, 167/85; pulse 108 (this is in reverse order starting about 10 minutes after the vaccine and ending about 15 minutes later when the ambulance arrived).
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Nifedipine ER 60mg, Gabapentin 300mg, Klor-Con 20mEq packets, Vitamin D2 50000IU, Montelukast 10mg, Bystolic 10mg, Torsemide 20mg, Omeprazole 20mg
- Allergien
- Diovan, Losartan, Aldactone
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 23.07.2021
- 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
Arthralgia
Blood creatinine increased
Blood pressure increased
Burning sensation
Butterfly rash
Carbon dioxide decreased
Feeling hot
Glomerular filtration rate decreased
Heart rate increased
Metabolic function test
Muscular weakness
Myalgia
Pain in extremity
Rash
Rash erythematous
Symptomtext
Hip and legs bone, muscle, muscle insertion extreme pain, increased heart rate, increased blood pressure, one episode of leg weakness, bright red lupus looking (malar) rash on face. It was hot to touch and burning. ER gave me toradol, steroids, and fluids. Facial rash and pain resolved that night. Bright red malar rash came back Saturday, Sunday, Monday.....comes back now when hot or out in the sun just on face.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Metabolic panel....Co2 low, creatinine high, GFR low
- Aktuelle Erkrankungen
- Sjogrens related dysautonomia, small fiber neuropathy, POTS, dryness (eyes, mouth), PCOS
- Vorgeschichte
- Sjogrens related dysautonomia, small fiber neuropathy, POTS, dryness (eyes, mouth), PCOS
- Andere Medikamente
- low dose naltrexone, HCQ, estradiol, pantoprazole, biotin, ketotifen, restasis, serum eye drops , vit c, salt
- Allergien
- sulfa, contrast media
- Vorherige Impfungen
- Flu shot/Oct 2020 rash on arm
- Staat
- MD
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 22.07.2021
- Impfdatum
- 21.07.2021
- Beginn
- 22.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Fatigue
Haematochezia
Pain
Symptomtext
large amount of blood in stool x 1 (so far) also with mild fatigue, body ache and abdominal cramping
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- constipation hair loss migraines irregular periods
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MS
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 19.07.2021
- Impfdatum
- 17.07.2021
- Beginn
- 19.07.2021
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site pain
Injection site pruritus
Injection site rash
Injection site warmth
Vaccination complication
Symptomtext
Patient has redness, itching, pain, heat and rash "covid arm" in left arm where she received vaccine. Pharmacist advised patient that she could take Benadryl (antihistamine) to help with reaction and follow up with primary care physician.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 16.07.2021
- Impfdatum
- 14.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Fatigue
Headache
Myalgia
Pyrexia
Symptomtext
Moderna COVID-19 Vaccine EUA Body/muscle aches, chills, low-grade fever, headache, and fatigue started around 12:24 am on 7/15/21, and lasted until midnight 7/16/21. Treated side effects with rest, liquids, Aleve, and warm bath. felt a little exhausted after side effects subsided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic migraines Anemia
- Andere Medikamente
- Camila birth control pills
- Allergien
- Cipro and Percocet: hives Tomatoes
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 15.07.2021
- Impfdatum
- 15.07.2021
- Beginn
- 15.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Dyschromatopsia
Hypoacusis
Laboratory test
Symptomtext
About 5 minutes after giving the patient the shot, patient started feeling very dizzy, when asked if he would like an ambulance he refused. After a few more minutes, patient said he was feeling a little better. No trouble breathing or talking. After a few more minutes patient started holding his ear and said he was having trouble hearing and started seeing colors. We asked if patient would like an ambulance and patient agreed. Paramedics came and did some tests.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 28.06.2023
- Impfdatum
- 08.10.2021
- Beginn
- 17.06.2023
- Tage bis Beginn
- 617,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note does not mention COVID (asymptomatic).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 8,0
- Labordaten
- COVID-19 detected PCR on 6/17/23.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Controlled type 2 diabetes mellitus, without long-term current use of insulin (Chronic) Essential hypertension (Chronic) Hyperlipidemia (Chronic) History of ischemic stroke (Chronic) Stroke-like symptoms History of CVA with residual deficit (Chronic) Major neurocognitive disorder due to vascular disease, without behavioral disturbance, severe Mixed hyperlipidemia Adenoma of colon at hepatic flexure Chronic pain of right lower extremity (Chronic) Weakness Chronic kidney disease, stage 3a (Chronic) Urinary incontinence (Chronic)
- Andere Medikamente
- -
- Allergien
- Latex, Natural Rubber Iodinated Contrast Media Shellfish Containing Products Penicillins Lactose
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 28.06.2023
- Impfdatum
- 08.10.2021
- Beginn
- 17.06.2023
- Tage bis Beginn
- 617,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
SARS-CoV-2 test positive
Symptomtext
Patient with history of COVID vaccines who admitted to hospital with COVID detected PCR. Provider d/c note does not mention COVID (asymptomatic).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 8,0
- Labordaten
- COVID-19 detected PCR on 6/17/23.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Controlled type 2 diabetes mellitus, without long-term current use of insulin (Chronic) Essential hypertension (Chronic) Hyperlipidemia (Chronic) History of ischemic stroke (Chronic) Stroke-like symptoms History of CVA with residual deficit (Chronic) Major neurocognitive disorder due to vascular disease, without behavioral disturbance, severe Mixed hyperlipidemia Adenoma of colon at hepatic flexure Chronic pain of right lower extremity (Chronic) Weakness Chronic kidney disease, stage 3a (Chronic) Urinary incontinence (Chronic)
- Andere Medikamente
- -
- Allergien
- Latex, Natural Rubber Iodinated Contrast Media Shellfish Containing Products Penicillins Lactose
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 25.04.2023
- Impfdatum
- 10.10.2021
- Beginn
- 24.02.2022
- Tage bis Beginn
- 137,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE Retrieving data. Wait a few seconds and try to cut or copy again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 28.03.2023
- Impfdatum
- 18.11.2021
- Beginn
- 27.05.2022
- Tage bis Beginn
- 190,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 2/8/21 Lot# 013M20A; Moderna 3/8/21 Lot# 030A21A; Moderna 11/18/21 Lot# 091D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 91,0
- Geschlecht
- M
- Eingang
- 27.03.2023
- Impfdatum
- 24.08.2021
- Beginn
- 25.03.2023
- Tage bis Beginn
- 578,0
- 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 7/27/21 Lot# 052C21A; Moderna 8/24/21 Lot# 091D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 02.01.2023
- Impfdatum
- 13.11.2021
- Beginn
- 28.12.2022
- Tage bis Beginn
- 410,0
- 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 4/22/21 Lot# 002C21A; Moderna 05/20/21 Lot# 002C21A; Moderna 11/13/21 Lot# 091D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID+
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 10.11.2022
- Impfdatum
- 05.11.2021
- Beginn
- 07.10.2022
- Tage bis Beginn
- 336,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cough
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cough
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 29.11.2021
- Beginn
- 28.10.2022
- Tage bis Beginn
- 333,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Admitted to hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 30.09.2022
- Impfdatum
- 23.11.2021
- Beginn
- 01.03.2022
- Tage bis Beginn
- 98,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Inflammatory marker increased
Symptomtext
I had routine blood work for my OBGYN and during that blood work my inflammation markers were slightly elevated. I was told to make dietary changes and will get a 2nd blood work next month.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood test
- Hospital-Tage
- -
- Labordaten
- Blood work- elevated inflammation markers.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Endometriosis; Monthly migraines
- Andere Medikamente
- Rizatriptan
- Allergien
- Preservative in Flu vaccine
- Vorherige Impfungen
- 15 years ago I had a Flu shot and almost fainted.
- Staat
- MI
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 11.08.2022
- Impfdatum
- 15.08.2021
- Beginn
- 10.08.2022
- Tage bis Beginn
- 360,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after two vaccines Moderna 7/13/21 Lot# 051C21A; Moderna 8/15/21 Lot#091D21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 20.07.2022
- Impfdatum
- 04.03.2021
- Beginn
- 01.06.2021
- Tage bis Beginn
- 89,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
Tinnitus both ears
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.07.2022
- Impfdatum
- 24.10.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
SARS-CoV-2 test
Suspected COVID-19
Symptomtext
Suspected Covid-19 Infection; Interchange of vaccine products; This spontaneous case was reported by a patient and describes the occurrence of SUSPECTED COVID-19 (Suspected Covid-19 Infection) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for Prophylactic vaccination. The occurrence of additional non-serious events is detailed below. Previously administered products included for Prophylactic vaccination: Jannsen covid-19 vaccine (Batch number 043A21A, dose number in series 1 and left arm) on 11-Apr-2021. Past adverse reactions to the above products included Vaccination failure with Jannsen covid-19 vaccine. Concurrent medical conditions included Exercise induced asthma. Concomitant products included FAMOTIDINE, CETIRIZINE HYDROCHLORIDE (ZYRTEC [CETIRIZINE HYDROCHLORIDE]), VITAMIN B COMPLEX, ALBUTEROL [SALBUTAMOL], COLECALCIFEROL (VITAMIN D [COLECALCIFEROL]) and MAGNESIUM for an unknown indication. On 24-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 24-Oct-2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products). On an unknown date, the patient experienced SUSPECTED COVID-19 (Suspected Covid-19 Infection) (seriousness criterion medically significant). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 21-May-2022 to 25-May-2022 for COVID-19, at an unspecified dose and frequency. On 09-Jun-2022, SUSPECTED COVID-19 (Suspected Covid-19 Infection) had resolved. At the time of the report, INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 29-May-2022, SARS-CoV-2 test: (Negative) Negative. On 30-May-2022, SARS-CoV-2 test: (Positive) Positive. On 09-Jun-2022, SARS-CoV-2 test: (Negative) Negative. Patient had no known allergy. 12 hours after taking 1st dose of paxlovid patient experienced very bitter ashy taste in mouth. Company comment: This spontaneous case concerns a patient of an unknown age and gender, with no relevant medical history, who experienced the unexpected, serious (due to medically significant) AESI of COVID-19, after the dose of mRNA-1273 vaccine, considered as the second dose of the vaccine schedule. Previously the patient received a dose of Jannsen covid-19 vaccine (interchange of vaccine products). As per source document, Paxlovid was prescribed as treatment. After a full course of Paxlovid the patient had recurrence of symptoms and tested positive on a rapid test. Twenty days after treatment the patient finally tested negative. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.; Sender's Comments: This spontaneous case concerns a patient of an unknown age and gender, with no relevant medical history, who experienced the unexpected, serious (due to medically significant) AESI of COVID-19, after the dose of mRNA-1273 vaccine, considered as the second dose of the vaccine schedule. Previously the patient received a dose of Jannsen covid-19 vaccine (interchange of vaccine products). As per source document, Paxlovid was prescribed as treatment. After a full course of Paxlovid the patient had recurrence of symptoms and tested positive on a rapid test. Twenty days after treatment the patient finally tested negative. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220529; Test Name: COVID-19 virus test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220530; Test Name: COVID-19 virus test; Test Result: Positive ; Result Unstructured Data: Positive; Test Date: 20220609; Test Name: COVID-19 virus test; Test Result: Negative ; Result Unstructured Data: Negative
- Aktuelle Erkrankungen
- Exercise induced asthma
- Vorgeschichte
- -
- Andere Medikamente
- FAMOTIDINE; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; VITAMIN B COMPLEX; ALBUTEROL [SALBUTAMOL]; VITAMIN D [COLECALCIFEROL]; MAGNESIUM
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 03.07.2022
- Impfdatum
- 11.04.2021
- Beginn
- 21.05.2022
- Tage bis Beginn
- 405,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysgeusia
SARS-CoV-2 test
Suspected COVID-19
Vaccination failure
Symptomtext
SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; VERY BITTER/ASHY TASTE IN MOUTH; This spontaneous report received from a patient via other manufacturer (Pfizer) concerned a patient of unspecified age, sex, race and ethnic origin. The patient's height, and weight were not reported. The patient's concurrent conditions included: exercise induced asthma, and The patient had no known drug allergy. The patient received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 043A21A expiry: unknown) 1 total, dose was not reported, administered on left arm on 11-APR-2021 for prophylactic vaccination. On 24-OCT-2021, the patient received non-company suspect vaccine included: Moderna/ spikevax (elasomeran) (dose number in series 2) (form of admin and route of admin were not reported, batch number: 091D21A expiry: unknown) dose was not reported, administered at left arm for prophylactic vaccination. Concomitant medications included cetirizine hydrochloride, vitamin d supplement, magnesium supplement, famotidine, salbutamol, and vitamin b complex. On an unspecified date, the patient experienced suspected covid-19 infection (dose number in series 2) and suspected clinical vaccination failure (dose number in series 1). The patient was prescribed with non-company suspect drug Paxlovid (form of admin and route of admin were not reported, batch number: GA3581, expiry: Unknown) dose was not reported administered first dose on 21-MAY-2022 and last dose on 25-MAY-2022 for treatment of covid 19. On 21-MAY-2022, 12 hours after the first dose of paxlovid, the patient experienced very bitter/ashy taste in mouth (dose number in series 2). On 29-MAY-2022, on day 9 after taking the full course of paxlovid, the patient tested negative for covid. On 30-MAY-2022, on day 10 after taking the full course of paxlovid, the patient had recurrence of symptoms (rebound covid) and tested positive on rapid test (dose number in series 2). On 09-JUN-2022, on day 20 after taking the full course of paxlovid, the patient finally tested negative on rapid test (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s, and elasomeran was not applicable. The patient recovered from suspected covid-19 infection on 09-JUN-2022, and very bitter/ashy taste in mouth on 27-MAY-2022, and the outcome of suspected clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000237574.; Sender's Comments: V0:20220649475-COVID-19 VACCINE AD26.COV2.S-Suspected clinical vaccination failure. The event(s) has an unknown/unclear temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysgeusia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220529; Test Name: COVID-19 TEST; Test Result: Negative ; Test Date: 20220530; Test Name: COVID-19 RAPID TEST; Test Result: Positive ; Test Date: 20220609; Test Name: COVID-19 RAPID TEST; Test Result: Negative
- Aktuelle Erkrankungen
- Exercise induced asthma
- Vorgeschichte
- Comments: The patient had no known drug allergy
- Andere Medikamente
- FAMOTIDINE; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; VITAMIN B COMPLEX; ALBUTEROL [SALBUTAMOL]; VITAMINE D
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 28.06.2022
- Impfdatum
- 01.09.2021
- Beginn
- 28.06.2022
- Tage bis Beginn
- 300,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID BREAKTHROUGH CASE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID+ 6/28/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CVA with residual left-sided deficits, DVT and PE on Xarelto, HTN, HLD, carotid dissection, obesity, seizure disorder on Keppra, May-Thurner syndrome
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 14.04.2022
- Beginn
- 02.05.2022
- Tage bis Beginn
- 18,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
After 2nd booster (April 14 2022) of Moderna vaccine, experienced breakthrough COVID 19 infection. Diagnosis was on 5/4/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test results, reported 5/5/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma, hypothyroidism
- Andere Medikamente
- Synthroid, estradiol, Montelukast, Bupropion, Pulmicort Flexhaler, vitamin
- Allergien
- Quinoline abc, Macrobid
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 05.02.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 52,0
- 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 GRANDMOTHER CALLED TO INFORM THAT PHARMACY VACCINATED PATIENT WITH MODERNA. PATIENT IS 17 YEARS OLD AND NOT REQUIRED TO RECEIVE MODERNA
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
- NONE
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 25.03.2022
- 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
No adverse event
Underdose
Symptomtext
Patient should have received 0.5mL but received 0.25mL instead. He has not had any adverse reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 02.03.2022
- Impfdatum
- 11.09.2021
- Beginn
- 22.01.2022
- Tage bis Beginn
- 133,0
- 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
- TN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 19.07.2021
- Beginn
- 16.02.2022
- Tage bis Beginn
- 212,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
27 hours at room temperature; more than 12 hours after the first puncture/Vaccine administered 24 hours after first puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (more than 12 hours after the first puncture/Vaccine administered 24 hours after first puncture) and PRODUCT STORAGE ERROR (27 hours at room temperature) in a 73-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 00J212A, 002FF21A and 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 19-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 16-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 16-Feb-2022 at 2:00 PM, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 16-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (more than 12 hours after the first puncture/Vaccine administered 24 hours after first puncture). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (27 hours at room temperature). At the time of the report, EXPIRED PRODUCT ADMINISTERED (more than 12 hours after the first puncture/Vaccine administered 24 hours after first puncture) and PRODUCT STORAGE ERROR (27 hours at room temperature) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant information was not provided. Vaccine stored in the refrigerator on 14-Feb-2022. Vial was first punctured on 15-Feb-2022 at 11:42AM. Administration of vaccine on 16-Feb-2022 at 2:00PM. Post puncture vial stored in room temperature. Treatment information was not provided. This case was linked to MOD-2022-494521 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 24-Feb-2022: Patient demographics and dose details added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 04.08.2021
- Beginn
- 04.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
patient received 2 different manufactured covid19 vacine; This spontaneous case was reported by a pharmacist and describes the occurrence of INTERCHANGE OF VACCINE PRODUCTS (patient received 2 different manufactured covid19 vacine) in a 51-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. Co-suspect product included non-company product COVID-19 VACCINE NRVV AD (CHADOX1 NCOV-19) (COVID-19 VACCINE ASTRAZENECA) for an unknown indication. No Medical History information was reported. In 2021, the patient received dose of COVID-19 VACCINE NRVV AD (CHADOX1 NCOV-19) (COVID-19 VACCINE ASTRAZENECA) (unknown route) 1 dosage form. On 04-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Aug-2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (patient received 2 different manufactured covid19 vacine). On 04-Aug-2021, INTERCHANGE OF VACCINE PRODUCTS (patient received 2 different manufactured covid19 vacine) outcome was unknown. 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. The pharmacist reported that the patient administered 1 dose of the moderna vaccine to three patients. Pharmacist reports that all three patients received a dose of the astrazeneca vaccine last month overseas No concomitant medication was reported. No treatment information was reported. Most recent FOLLOW-UP information incorporated above includes: On 12-Aug-2021: Follow-up information included race and ethnicity was added
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 34,0
- Geschlecht
- U
- Eingang
- 26.02.2022
- Impfdatum
- 29.07.2021
- Beginn
- 29.07.2021
- 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
Patient received a vaccine from a vial that was exposed to room temperature for 19 hours; This case was received via a Regulatory Authority (Reference number: US-irms-MOD21-125183) on 30-Jul-2021 and was forwarded to Moderna on 30-Jul-2021. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received a vaccine from a vial that was exposed to room temperature for 19 hours) in a 34-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 29-Jul-2021, 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 29-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received a vaccine from a vial that was exposed to room temperature for 19 hours). On 29-Jul-2021, EXPIRED PRODUCT ADMINISTERED (Patient received a vaccine from a vial that was exposed to room temperature for 19 hours) 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 medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient was given a dose of the vaccine from an expired vial; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was given a dose of the vaccine from an expired vial) in a 43-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 27-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was given a dose of the vaccine from an expired vial). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient was given a dose of the vaccine from an expired vial) 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. Concomitant product use was not provided by the reporter. Treatment information was not reported. This case was linked to US-MODERNATX, INC.-MOD-2021-268121 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- 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
Patient was given a dose of the vaccine from an expired vial; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was given a dose of the vaccine from an expired vial) in a 55-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 27-Jul-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was given a dose of the vaccine from an expired vial). On 27-Jul-2021, EXPIRED PRODUCT ADMINISTERED (Patient was given a dose of the vaccine from an expired vial) 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. Pharmacist stated that this morning, a couple doses of the Moderna Covid-19 vaccine was given from a bottle that was left out from yesterday. The vial was first punctured at 8:52 am yesterday 26/Jul/2021 and left at room temperature. It was administered today at 12:03 pm and 12:16 pm, 2 doses were given. Lot number is 091D21A, one vial. This lot number had not undergone any excursion. Upon inspection before administration, the vaccine was thawed, and it looked normal. it was the first doses for both patients that received the vaccine and caller stated that none of the patients had reported any adverse event. This case was linked to US-MODERNATX, INC.-MOD-2021-268254 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2021-268254:Same reporter (CASE CROSSLINKED)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 22.07.2021
- Beginn
- 22.07.2021
- 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
Device connection issue
Symptomtext
wrong with the syringe; most of the vaccine dose went down the patients arm; This spontaneous case was reported by a pharmacist and describes the occurrence of ACCIDENTAL UNDERDOSE (most of the vaccine dose went down the patients arm) and DEVICE CONNECTION ISSUE (wrong with the syringe) in a 51-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. 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 22-Jul-2021, the patient experienced ACCIDENTAL UNDERDOSE (most of the vaccine dose went down the patients arm). On an unknown date, the patient experienced DEVICE CONNECTION ISSUE (wrong with the syringe). At the time of the report, ACCIDENTAL UNDERDOSE (most of the vaccine dose went down the patients arm) had resolved and DEVICE CONNECTION ISSUE (wrong with the syringe) 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 medications were reported. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 10-Aug-2021: Follow-up received non significant fax number added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 21.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
expired on 12-Feb-2022 and a dose was given on 14-Feb-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired on 12-Feb-2022 and a dose was given on 14-Feb-2022) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Feb-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired on 12-Feb-2022 and a dose was given on 14-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired on 12-Feb-2022 and a dose was given on 14-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment information was provided. The Moderna had been in the refrigerator for ten days and there had been no temp excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 23.06.2021
- Beginn
- 11.02.2022
- Tage bis Beginn
- 233,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Exposure to SARS-CoV-2
Muscular weakness
SARS-CoV-2 test
Urinary tract infection
Symptomtext
Pt was admitted on 12/21/2021 for bilateral lower extremity weakness and a UTI. He was tested for COVID due to his wife testing positive and being his visitor over the last 2 months.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exposure to SARS-CoV-2
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 26.10.2021
- Beginn
- 09.02.2022
- Tage bis Beginn
- 106,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Angiogram
Blood culture
Computerised tomogram head
Fibrin D dimer
Full blood count
Mental status changes
Metabolic function test
Urine analysis
Symptomtext
Altered Mental Status
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Angiogram
- Hospital-Tage
- -
- Labordaten
- CT Angio 2/10/21, CT Head 2/10/21, CMP 2/10/21, CBC 2/10/21, Urine Toxicology screen 2/10/21, CXR 2/10/21, Blood cultures 2/10/21, D-Dimer 2/10/21.
- Aktuelle Erkrankungen
- Altered Mental Status
- Vorgeschichte
- Angina Pectoris, Back pain, GERD, Iron Deficiency Anemia, Pure Hypercholesterolemia, Arteriosclerosis of coronary artery, HTN, Skin Cancer, Osteoarthritis
- Andere Medikamente
- Furosemide 40 mg daily, NTG 0.4 mg SL PRN, KCL 20 mEq PO TID, Amlodipine 5 mg PO BID, Colace 100 mg PO BID, Esomeprazole 40 mg PO daily, Zetia 10 mg PO daily, Xarelto 20 mg PO daily, Aspirin 81 mg PO daily, Vitamin D3 25 mcg 3 caps PO dail
- Allergien
- Codeine, Gabapentin, Duloxetine
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 11.10.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 71,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Exposure during pregnancy
Foetal hypokinesia
SARS-CoV-2 test positive
Symptomtext
12/21/21 presents to triage for "decreased fetal mvoement since this afternoon. Patient scheduled for induction tomorrow morning". PMHx of "asthma, left breast mass"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 12/22/21 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 11.08.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 82,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erectile dysfunction
Symptomtext
Erectile dysfunction; This spontaneous case was reported by a consumer and describes the occurrence of ERECTILE DYSFUNCTION (Erectile dysfunction) in a 26-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 004F21A and 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 09-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In November 2021, the patient experienced ERECTILE DYSFUNCTION (Erectile dysfunction) (seriousness criterion medically significant). At the time of the report, ERECTILE DYSFUNCTION (Erectile dysfunction) outcome was unknown. No concomitant medications were reported. No treatment information was provided by the reporter. Two months after the second shot, patient started having erectile dysfunction. Patient wanted to know the incidence of this side effect. Patient was not seen by the doctor for this, but an appointment was made. Both doses were injected into the upper arm. Company comment: This case concerns a 26-year-old male patient with no medical history provided who experienced serious unexpected event of Erectile dysfunction. The event occurred approximately two months after the second dose of the mRNA-1273 vaccine. At the time of the report, the outcome of the event was unknown and no information regarding the clinical course of the event was provided. No information regarding patient's medical history, concomitant medications nor treatment medications was provided. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This case concerns a 26-year-old male patient with no medical history provided who experienced serious unexpected event of Erectile dysfunction. The event occurred approximately two months after the second dose of the mRNA-1273 vaccine. At the time of the report, the outcome of the event was unknown and no information regarding the clinical course of the event was provided. No information regarding patient's medical history, concomitant medications nor treatment medications was provided. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erectile dysfunction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 27.07.2021
- Beginn
- 20.01.2022
- Tage bis Beginn
- 177,0
- Dosis
- 2
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
admitted to hospital with breakthrough covid infection 1/20/22
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 3,0
- Labordaten
- COVID PCR positive 1/20/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 30.09.2021
- Beginn
- 04.01.2022
- Tage bis Beginn
- 96,0
- Dosis
- UNK
- Route/Site
- IM / LA
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
- WI
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 05.01.2022
- Impfdatum
- 12.10.2021
- Beginn
- 03.01.2022
- Tage bis Beginn
- 83,0
- Dosis
- 2
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Infection
SARS-CoV-2 test positive
Symptomtext
COVID-19 breakthrough infection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Infection
- Hospital-Tage
- -
- Labordaten
- NAAT 1/3/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 18,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
Pt developed s/s causing him to be taken to the ED and admitted to the hospital, COVID positive on admission
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 12/21- SARS Coronavirus-2, PCR detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 16.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SC / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
Symptomtext
Vaccine given subcutaneously, not IM as required.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Obesity Others unknown
- Andere Medikamente
- Unknown and not relevant
- Allergien
- Unknown and not relevant
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 08.12.2021
- Impfdatum
- 20.07.2021
- Beginn
- 21.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia oral
Symptomtext
Patient STARTED EXPERIENCING NUMBNESS ON THE TIP OF HIS TONGUE AFTER THE ADMINISTRATION OF SECOND DOSE OF COVID VACCINE. HE WAITED FOR FEW MONTHS HOPING TO EVENTUALLY GET BETTER BU IT DID NOT GET BETTER. HE CALLED PHARMACY ON 12/08/21 TO REPORT THE POSSIBLE SIDE EFFECT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypoaesthesia oral
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 26.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anxiety
Depression
Impaired work ability
Morbid thoughts
Suicidal ideation
Symptomtext
After every COVID vaccination, including booster, about one week later I'd enter a severe depression and have severe anxiety. I have had these feelings before and know well how to handle them and cope. But this was consistent with every dose despite my life circumstances. The intensity was severe, needing me to reach out to my doctors and for help from my family every time. Every time I had to take time off work. After the booster, the depression and anxiety became so severe that I had to check myself into the emergency room to not take my own life. I had a hard time getting help because of the anxiety. And the thoughts in my head were darker then anything I have ever experienced. This occurred 5-7 days after every vaccine. And each time I got another one, the symptoms would persist for longer. If I hadn't had a psychology degree and known to get help for those thoughts, it is very likely that I could have died.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anxiety
- Hospital-Tage
- 1,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Scoliosis, Hypothyroidism
- Andere Medikamente
- Levothyroxine 50mcg, Blisovi FE 1/20
- Allergien
- Septra/Sulfa, most antibiotics
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 03.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- 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
Incorrect dose administered
Symptomtext
Patient received 0.5mL instead of 0.25mL for Moderna booster vaccine. Provider informed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Patient Received 0.5ml instead of 0.25ml for Moderna booster vaccine. Provider informed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
My staff missed seeing that this individual was not old enough for the Moderna vaccine. Her mom works at the same facility and has been notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 27.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 24,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acoustic stimulation tests
Deafness
Hypoacusis
Sudden hearing loss
Symptomtext
lost most of the hearing in my good ear/been unable to hear from her right (good) ear; people were talking and I couldn't understand anything when people were talking, she could not understand what they were saying. The words were not clear; All of a sudden, when she got up in the morning, she couldn't hear anything; This spontaneous case was reported by a consumer and describes the occurrence of SUDDEN HEARING LOSS (All of a sudden, when she got up in the morning, she couldn't hear anything) and DEAFNESS (lost most of the hearing in my good ear/been unable to hear from her right (good) ear) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Deafness left ear. Concomitant products included COLECALCIFEROL (VITAMIN D3), FLUOXETINE HYDROCHLORIDE (PROZAC), ATORVASTATIN, METOPROLOL, ATORVASTATIN CALCIUM (LIPITOR), ZOLPIDEM TARTRATE (AMBIEN), LORAZEPAM (ATIVAN) and CETIRIZINE HYDROCHLORIDE (ZYRTEC ALLERGY) for an unknown indication. On 25-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Nov-2021, the patient experienced SUDDEN HEARING LOSS (All of a sudden, when she got up in the morning, she couldn't hear anything) (seriousness criterion medically significant) and HYPOACUSIS (people were talking and I couldn't understand anything when people were talking, she could not understand what they were saying. The words were not clear). On an unknown date, the patient experienced DEAFNESS (lost most of the hearing in my good ear/been unable to hear from her right (good) ear) (seriousness criterion medically significant). At the time of the report, SUDDEN HEARING LOSS (All of a sudden, when she got up in the morning, she couldn't hear anything), DEAFNESS (lost most of the hearing in my good ear/been unable to hear from her right (good) ear) and HYPOACUSIS (people were talking and I couldn't understand anything when people were talking, she could not understand what they were saying. The words were not clear) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 19-Nov-2021, Acoustic stimulation tests: hearing has gone down to 50% of original (abnormal) Hearing has gone down to 50% of original. No treatment information was reported. Company comment: This case concerns a 78 year old female with relevant medical history of Deafness in the left ear, who experienced Serious ( medically significant ) unexpected events of Sudden hearing Loss , Deafness and non-serious unexpected event of hypoacusis which occurred 25 days after vaccination with the 3rd dose ( booster dose) of mRNA-1273 vaccine ( Moderna Covid 19 Vaccine). Acoustic stimulation test was done which showed that the hearing went down by 50% in the right ear. The re-challenge for this case is not applicable since the events outcome were reported as unknown and the events reported occurred on the 3rd dose ( booster dose ) and no additional doses will be given. The age of the patient and the condition of hearing loss in the L ear is a confounder for this case . ( elderly patients are prone to hearing loss as a result of aging) . The benefit -risk relationship of mRNA -1273 ( Moderna Covid 19 Vaccine) is not affected by this report.; Sender's Comments: This case concerns a 78 year old female with relevant medical history of Deafness in the left ear, who experienced Serious ( medically significant ) unexpected events of Sudden hearing Loss , Deafness and non-serious unexpected event of hypoacusis which occurred 25 days after vaccination with the 3rd dose ( booster dose) of mRNA-1273 vaccine ( Moderna Covid 19 Vaccine). Acoustic stimulation test was done which showed that the hearing went down by 50% in the right ear. The re-challenge for this case is not applicable since the events outcome were reported as unknown and the events reported occurred on the 3rd dose ( booster dose ) and no additional doses will be given. The age of the patient and the condition of hearing loss in the L ear is a confounder for this case . ( elderly patients are prone to hearing loss as a result of aging) . The benefit -risk relationship of mRNA -1273 ( Moderna Covid 19 Vaccine) is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acoustic stimulation tests
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211119; Test Name: Hearing tests; Result Unstructured Data: Hearing has gone down to 50% of original
- Aktuelle Erkrankungen
- Deafness left ear
- Vorgeschichte
- -
- Andere Medikamente
- VITAMIN D3; PROZAC; ATORVASTATIN; METOPROLOL; LIPITOR; AMBIEN; ATIVAN; ZYRTEC ALLERGY
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 26.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administration error
Symptomtext
Provider asked the LPN to administer a covid vaccine. There was no order in the chart. The patients father was upset about the wait time and yelling at staff. The LPN got in a hurry and drew up the vaccine, administered it and did not do her vaccine double check .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administration error
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 22.11.2021
- Impfdatum
- 13.10.2021
- Beginn
- 13.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient was given the Moderna Vaccine and should have received the Pfizer vaccine due to his age. No reactions reported from giving the vaccine. Parent was notified of error on the vaccine and also spoke to representative who advised to proceed with Moderna again for his 2nd dose to complete the series
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 16.11.2021
- Impfdatum
- 13.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Administration error - Patient received 5ml patient instead of .5ml of vaccination. (Moderna)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None.
- Andere Medikamente
- -
- Allergien
- none.
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 16.11.2021
- Impfdatum
- 13.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 19,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bronchitis
Cough
Magnetic resonance imaging
Productive cough
Rales
Respiratory disorder
Secretion discharge
Wheezing
X-ray
Symptomtext
respiratory issue; my lungs crackle; inhale and wheeze/lungs wheeze and crackle; like having bronchitis; terrible cough/horsy cough/cough and more and more mucus keeps coming on/lots of phlegm kept coming back; more and more mucus keeps coming on; lots of phlegm kept coming back; This spontaneous case was reported by a consumer and describes the occurrence of RESPIRATORY DISORDER (respiratory issue), RALES (my lungs crackle), WHEEZING (inhale and wheeze/lungs wheeze and crackle), BRONCHITIS (like having bronchitis) and COUGH (terrible cough/horsy cough/cough and more and more mucus keeps coming on/lots of phlegm kept coming back) in a 65-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 046C21A and 091D21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concomitant products included ALBUTEROL [SALBUTAMOL] for Asthma. On 13-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Sep-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In September 2021, the patient experienced RESPIRATORY DISORDER (respiratory issue), RALES (my lungs crackle), WHEEZING (inhale and wheeze/lungs wheeze and crackle), BRONCHITIS (like having bronchitis), COUGH (terrible cough/horsy cough/cough and more and more mucus keeps coming on/lots of phlegm kept coming back), SECRETION DISCHARGE (more and more mucus keeps coming on) and PRODUCTIVE COUGH (lots of phlegm kept coming back). At the time of the report, RESPIRATORY DISORDER (respiratory issue), RALES (my lungs crackle), WHEEZING (inhale and wheeze/lungs wheeze and crackle), BRONCHITIS (like having bronchitis), COUGH (terrible cough/horsy cough/cough and more and more mucus keeps coming on/lots of phlegm kept coming back), SECRETION DISCHARGE (more and more mucus keeps coming on) and PRODUCTIVE COUGH (lots of phlegm kept coming back) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Magnetic resonance imaging: normal (normal) normal. On an unknown date, X-ray: normal (normal) Normal. No concomitant medication was provided. Doctor gave antibiotics which seemed to subside the problem but after that it went back. So patient got a second set of antibiotics for 10 more days. Patient said that he has been having this issue for around 2 months
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bronchitis
- Hospital-Tage
- -
- Labordaten
- Test Name: MRI; Result Unstructured Data: normal; Test Name: X-ray; Result Unstructured Data: Normal
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ALBUTEROL [SALBUTAMOL]
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 7,0
- Geschlecht
- M
- Eingang
- 15.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- 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
Moderna Booster dose (0.25ml) inadvertently given to 7 year old
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- -
- Andere Medikamente
- No medications
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 9,0
- Geschlecht
- M
- Eingang
- 15.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- 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
Moderna Booster Dose (0.25ml) inadvertently given to 9 year old.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- -
- Andere Medikamente
- No medications
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 11,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Moderna Booster Dose (0.25ML) inadvertently given to 11 year old.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Asthma
- Andere Medikamente
- Albuterol inhaler, multivitamin, Advair, Xopenex
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysgeusia
Feeding disorder
Parosmia
Taste disorder
Symptomtext
Hard time eating OR drinking something that she can withstand; Everything tastes like rot; Everything smells like rot; Metallic taste; This spontaneous case was reported by a consumer and describes the occurrence of DYSGEUSIA (Metallic taste), TASTE DISORDER (Everything tastes like rot), PAROSMIA (Everything smells like rot) and FEEDING DISORDER (Hard time eating OR drinking something that she can withstand) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 27-Oct-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-Oct-2021, the patient experienced DYSGEUSIA (Metallic taste). On 29-Oct-2021, the patient experienced TASTE DISORDER (Everything tastes like rot) and PAROSMIA (Everything smells like rot). On an unknown date, the patient experienced FEEDING DISORDER (Hard time eating OR drinking something that she can withstand). At the time of the report, DYSGEUSIA (Metallic taste), TASTE DISORDER (Everything tastes like rot), PAROSMIA (Everything smells like rot) and FEEDING DISORDER (Hard time eating OR drinking something that she can withstand) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient stated that she called her doctor and she said that she doesn't deal with Moderna vaccine" also mentioned that pharmacy was also not able to help her. No concomitant medications were mentioned. No treatment details were reported. This case was linked to MOD21-161833 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysgeusia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 70-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by another health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 62-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). On 03-Nov-2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not provided Treatment medications were not provided It was reported that 4 vials (15 dose). 44 doses. vials were stored in the refrigerator on 24-sep-2021. Vaccine was administration between 24Oct2021 - 27Oct2021. vials did not undergo any temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 82,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- -
- Beginn
- 03.11.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in an 82-year-old patient of an unknown gender who received mRNA-1273 (COVID 19 Vaccine Moderna) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (COVID 19 Vaccine Moderna) (unknown route) 1 dosage form. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). On 03-Nov-2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (COVID 19 Vaccine Moderna) (Unknown), the reporter did not provide any causality assessments. No concomitant medication reported. No treatment medication reported. Date of the vials was initially stored in the refrigerator: 24Sept2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 74-year-old patient of an unknown gender who received mRNA-1273 (COVID 19 Vaccine Moderna) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (COVID 19 Vaccine Moderna) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (COVID 19 Vaccine Moderna) (Unknown), the reporter did not provide any causality assessments. Date of administration of vaccine was between 24Oct2021 - 27Oct2021. No concomitant information was reported. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 70-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided by reporter. 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
- TX
- Alter
- 65,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- 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
Expired product administered
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 65-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 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. In October 2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) 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. Most recent FOLLOW-UP information incorporated above includes: On 03-Nov-2021: Patient details and suspect drug details updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 28,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 28-year-old patient of an unknown gender who received mRNA-1273 (COVID 19 Vaccine Moderna) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (COVID 19 Vaccine Moderna) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (COVID 19 Vaccine Moderna) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported. Date of administration of vaccine: 24-OCT-2021 - 27-OCT-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 59-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided No treatment medication information was provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 87,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in an 87-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant information was reported. No treatment information was reported. Reporter has stated that the vaccine was administered between 24Oct2021 - 27Oct2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 90,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 90-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not provided. Treatment information was not provided. The patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) on 24Oct2021 - 27Oct2021. Date the vial was initially stored in the refrigerator is24-Sept-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vaccine that was given after the expiration date.) in a 67-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. On 24-Sep-2021, the vial was initially stored in the refrigerator. The vaccine was administered between 24-Oct-2021 to 27-Oct-2021. The vial had not undergone any temperature excursions. Concomitant medication information not provided. Treatment information not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 69-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. No treatment medication was provided. This case was linked to MOD-2021-374648, MOD-2021-374432, MOD-2021-374264 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- -
- Beginn
- 03.11.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by a health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 71-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) 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 concomitants are provided No treatments are provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 26,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 26-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). On 03-Nov-2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication provided No treatment medication provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 72-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had 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. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by a health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 52-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Date the vial was initially stored in the refrigerator-24Sept2021 No concomitant medications were provided. 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
- TX
- Alter
- 69,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- 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
Symptomtext
Moderna Covid-019 vaccine was given after the expiration date.; This spontaneous case was reported by a health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED ( Moderna Covid-019 vaccine was given after the expiration date.) in a 69-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED ( Moderna Covid-019 vaccine was given after the expiration date.). On 03-Nov-2021, EXPIRED PRODUCT ADMINISTERED ( Moderna Covid-019 vaccine was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Number of doses/vials: 4 vials (15 dose). 44 doses Date the vial was initially stored in the refrigerator: 24Sept2021 Date(s) of administration of vaccine: 24Oct2021 - 27Oct2021 Consent given for Safety follow up/contact with caller. No concomitant medications were administered. 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
- TX
- Alter
- 70,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 70-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. no concomitants were reported. no treatment medications was provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 76,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by a health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 76-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Treatment medication was not provided. Concomitant medication was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
Vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine that was given after the expiration date.) in a 70-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (Vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product information was not provided. Treatment information was not reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- -
- Beginn
- 03.11.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 74-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). On 03-Nov-2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No relevant concomitant medication was reported. Treatment information were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 59-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that Number of doses vials were 4 vials (15 dose) given for 44 patients. and date the vial was initially stored in the refrigerator was 24Sept2021. 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
- TX
- Alter
- 60,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 60-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not provided. Treatment medications were not provided. It was reported that there were 4 vials (15 dose) 44 doses. The vial was initially stored in the refrigerator on 24-Sep-2021. Vaccine was administered between 24Oct2021 - 27Oct2021. The vials did not undergo any temperature excursions. This case was linked to MOD-2021-374648, MOD-2021-374935, MOD-2021-374432 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- 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
Expired product administered
Symptomtext
We have some Moderna Covid-19 vaccine that was given after the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-19 vaccine that was given after the expiration date) in a 55-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 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. In October 2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-19 vaccine that was given after the expiration date). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-19 vaccine that was given after the expiration date) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. 4 vials with 44 doses were initially stored in the refrigerator on 24-Sep-2021 and did not undergo any temperature excursion. Dosing was done between 24-Oct-2021 - 27-Oct-2021. No concomitant medication was reported by reporter. No treatment medication was reported by reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- -
- Beginn
- 03.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 78-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). On 03-Nov-2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) 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 information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 68-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant information was reported. No treatment information was reported. Date of administration of vaccine was 24-Oct-2021 to 27-Oct-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- -
- Beginn
- 03.11.2021
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 78-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third 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 and first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. no concomitant and treatment drugs were provided. Date the vial was initially stored in the refrigerator: 24Sept2021 o*Date(s) of administration of vaccine: 24Oct2021 - 27Oct2021 This case was linked to MOD-2021-374935 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 42-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. No treatment information was provided. It was reported that the patient received Moderna COVID-19 vaccine that was given after the expiration date. The date of administration of vaccine was between 24-Oct-2021 to 27-Oct-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 27,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 27-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. 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, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment medications were provided. Date the vial was initially stored in the refrigerator 24Sept 2021 Date of administration of vaccine 24Oct2021 - 27Oct 2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- -
- Beginn
- 03.11.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 64-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). On 03-Nov-2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Date the vial was initially stored in the refrigerator 24- Sept-2021. Date of administration of vaccine 24Oct2021 - 27Oct2021 No concomitant medications was reported. no treatment was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- -
- Beginn
- 03.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 74-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). On 03-Nov-2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that date the vial was initially stored in the refrigerator 24-Sep-2021.Date of administration of vaccine 24-Oct-2021 - 27-Oct-2021. 44 doses were stored in refrigerator. Concomitant medications was not provided by the reporter. Treatment information was not provided. This case was linked to MOD-2021-374935, MOD-2021-374694 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 65-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications provided. No treatment medications provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 78-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). On 03-Nov-2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The vial was initially stored in refrigerator on 24-Sep-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 27,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 27-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. No treatment information was provided. Date the vial was initially stored in the refrigerator: 24-Sept-2021. Date(s) of administration of vaccine: 24-Oct-2021-27-Oct-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). On 03-Nov-2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitants drugs were reported. No treatment drug was reported The vial was initially stored in the refrigerator on 24Sept2021 No temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 80,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in an 80-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). On 03-Nov-2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. Treatment information was unknown. On 24-Sep-2021, the vial was initially stored in the refrigerator. 4 vials (15 dose). 44 doses were used.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 32,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 32-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were provided. No treatment medication was provided. Date the vial was initially stored in the refrigerator was 24-Sep-2021. Date of administration of vaccine was 24-Oct-2021 - 27-Oct-2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 24.10.2021
- Tage bis Beginn
- 23,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Moderna Covid-019 vaccine that was given after the expiration date; This spontaneous case was reported by a consumer and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna Covid-019 vaccine that was given after the expiration date) in a 72-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 24-Oct-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna Covid-019 vaccine that was given after the expiration date). On 27-Oct-2021, EXPIRED PRODUCT ADMINISTERED (Moderna Covid-019 vaccine that was given after the expiration date) had resolved. No concomitant medications were provided. No treatment medications were reported. Date of administration of vaccine: 24Oct2021 - 27Oct2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 81,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- 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
Expired product administered
Symptomtext
We have some Moderna Covid-19 vaccine that was given after the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-19 vaccine that was given after the expiration date) in an 81-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 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. In October 2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-19 vaccine that was given after the expiration date). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-19 vaccine that was given after the expiration date) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. 4 vials were stored in refrigerator 24-Sep-2021 with no temperature excursions. Dose was given on between 24-Oct-2021 to 27-Oct-2021. No concomitant medication was reported by reporter. No treatment medication was reported by reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 81,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna COVID-19 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna COVID-19 vaccine that was given after the expiration date.) in an 81-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna COVID-19 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna COVID-19 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant information was not provided. Treatment information was not provided. Date the vial was initially stored in the refrigerator: 24-Sept-2021. Date(s) of administration of vaccine: 24Oct2021 - 27Oct2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 30,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 30-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment medications were provided. The vial was initially stored in the refrigerator on 24 Sep 2021 . The vial did not undergo any temperature excursion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- U
- Eingang
- 12.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna COVID-19 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna COVID-19 vaccine that was given after the expiration date.) in a 69-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna COVID-19 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna COVID-19 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant information was not provided. It was reported that the vial was initially stored in refrigerator on 24 -Sep-2021.And the date of administration of vaccine was from 24-Oct-2021 to 27-Oct-2021..The vial didn't undergone any temperature excursions. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 03.11.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by a health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Nov-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). On 03-Nov-2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) 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. It was reported that number of doses/vials were 4 vials (15 dose) 44 doses. It was reported that the date the vial initially stored in the refrigerator 24-Sep-2021. It was also reported that the date of administration of vaccine was 24-Oct-2021 to 27-Oct-2021. The vial did not undergo any temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- U
- Eingang
- 11.11.2021
- Impfdatum
- 01.10.2021
- Beginn
- 01.10.2021
- 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
Symptomtext
We have some Moderna Covid-019 vaccine that was given after the expiration date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) in a 69-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. In October 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In October 2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.). In October 2021, EXPIRED PRODUCT ADMINISTERED (We have some Moderna Covid-019 vaccine that was given after the expiration date.) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. 4 vials with 44 doses were initially stored in the refrigerator on 24-SEP-2021 and did not undergo any temperature excursion. Dosing was done between 24Oct2021 - 27Oct2021. No concomitant medications were provided. 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
- TX
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 09.11.2021
- Impfdatum
- 23.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Symptomtext
I had shingles appear on the left trunk of my body and was prescribed Valtrex by my health care provider. I have taken the medication for the past eight days and symptoms have greatly improved and currently mild.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Turner?s Syndrome, Bicuspid Aortic Heart Valve, Ocular Rosacea, Depression, High Blood Pressure, and previously diagnosed with Melanoma skin cancer.
- Andere Medikamente
- Effexor, Lisinopril, Pirmella, Fish Oil, Evening Primrose, Flax Seed Oil, Multivitamin, Ginger Root, Probiotic
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 09.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong product administered
Symptomtext
Patient was given Booster dose ( 0.25 ml) of the Moderna Vaccine instead of Fluad. Pt did not have any reaction at the time she left the pharmacy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
The patient was brought to the clinic by her daughter and grand daughter for evaluation of dementia and other chronic conditions and acute complaints. Her daughter said that while she is here she would like to get her vaccinated against COVID, because she said that the patient had not gotten her COVID vaccine yet. She was given the Moderna Vaccine 0.5 mL and given a Vaccine card with the return date for the 2nd dose. On 11-04-2021 when billing was being conducted, there was a question about previous COVID vaccines being given. At this time WEB IZ was accessed and it was discovered that the patient had gotten a dose of MODERNA on 07/14/2021 and 08/13/2021 at other facilities. The patient's caregiver has been contacted and reports no negative effects or events up to this point. She was instructed that for any signs of reaction or any change in the patient's status that the patient is to be evaluated immediately.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Dementia, A-fib, CHF, Osteoporosis, Prediabetes, COPD, CKD
- Vorgeschichte
- Dementia, A-fib, CHF, Osteoporosis, Prediabetes, COPD, CKD
- Andere Medikamente
- Taking predniSONE 10 MG Tablet 1 tablet Orally Once a day, Taking Oxygen 2LPM as directed NASAL CANULA , Notes: 3L PRN, Taking Cyproheptadine HCl 4 MG Tablet 1 tablet Orally Twice a day, Taking Donepezil HCl 5 MG Tablet 1 tablet at bedtime
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/28
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/28
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/28
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 90,0
- Geschlecht
- U
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/28
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/28.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/28
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/28
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- U
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/28
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- U
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/28
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/28
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/28
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 28.10.2021
- Beginn
- 28.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/28
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
expired vial 10/24 administered on 10/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vial 10/24/2021 administered 10/27/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/27.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 87,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/27.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 27.10.2021
- Beginn
- 27.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/27
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vial 10/24 administered on 10/25
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vial 10/24 administered on 10/26
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired Vial 10/24 administerd on 10/26
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered on 10/26.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vial 10/24/2021 administered 10/26/2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 - administered on 10/26
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 - administered on 10/26
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vial 10/24 administered 10/26
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 - administered 10/26
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered 10/26
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 70,0
- Geschlecht
- U
- Eingang
- 03.11.2021
- Impfdatum
- 26.10.2021
- Beginn
- 26.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vial 10/24 administered on 10/25
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 - administered on 10/25.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 03.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
expired vial 10/24 administered 10/25
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired via 10/24 administered 10/25
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vial expired 10/24/21 - administered 10/25
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 25.10.2021
- Beginn
- 25.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Expired vial 10/24 - administered on 10/25
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- -
- Beginn
- 24.10.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Swollen tongue
Tongue disorder
Symptomtext
about a quarter inch swollen/ my tongue is swollen; tongue feels thicker; This spontaneous case was reported by a consumer and describes the occurrence of SWOLLEN TONGUE (about a quarter inch swollen/ my tongue is swollen) and TONGUE DISORDER (tongue feels thicker) in an 80-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. Concurrent medical conditions included Chronic bronchitis. Concomitant products included FLUTICASONE FUROATE, UMECLIDINIUM BROMIDE, VILANTEROL TRIFENATATE (TRELEGY) for Chronic bronchitis. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 24-Oct-2021, the patient experienced SWOLLEN TONGUE (about a quarter inch swollen/ my tongue is swollen) and TONGUE DISORDER (tongue feels thicker). At the time of the report, SWOLLEN TONGUE (about a quarter inch swollen/ my tongue is swollen) and TONGUE DISORDER (tongue feels thicker) outcome was unknown. It was reported that the patient had completed the series of Moderna COVID-19 Vaccination in Feb-2021 and did not experienced this symptoms. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Swollen tongue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Chronic bronchitis
- Vorgeschichte
- -
- Andere Medikamente
- TRELEGY
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 31.10.2021
- 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
Muscular weakness
Symptomtext
Patient reports experiencing weakness in her legs the evening of vaccine administration. She claims it was so severe she was unable to get out of bed without assistance. She states there was a little improvement in her condition by the next morning and that she gradually returned to normal over the course of the next few days. Patient states she did not seek any medical help for her condition and is feeling fine at present.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Muscular weakness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 26.10.2021
- 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: nein
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 25.10.2021
- Impfdatum
- 23.10.2021
- Beginn
- 23.10.2021
- 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
We gave a Moderna shot to a 12 years old who is not eligible for the shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 22.10.2021
- 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: nein
Incorrect dose administered
Symptomtext
patient given 0.5 ml instead of .25 ml as a booster. Patient has chronic conditions but not immune compromized.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None reported yet.
- Aktuelle Erkrankungen
- none reported
- Vorgeschichte
- None reported
- Andere Medikamente
- spironolactone , pravastatin, atenolol, furosemide,
- Allergien
- no known allergy
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 22.10.2021
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- 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
Incorrect dose administered
Symptomtext
ADMINISTERED 0.5 ML OF MODERNA BOOSTER INTRAMUSCULARLY INSTEAD OF 0.25 ML RECOMMENDED DOSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 22.10.2021
- Impfdatum
- 21.10.2021
- Beginn
- 21.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
ADMINISTERED 0.5 ML OF MODERNA BOOSTER INSTEAD OF 0.25 ML RECOMMENDED DOSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 22.10.2021
- Impfdatum
- 22.10.2021
- Beginn
- 22.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Administered expired dose of moderna to patient. Vial expired at 0358AM on 10/22/21 and the vaccine was administered at 08:50AM on 10/22/21. Vial opened at 1558 on 10/22/21 and placed in room temperature
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Active Problems Diabetic macular edema (H) Insulin dependent diabetes mellitus with complications Lumbar Radiculopathy At L5 Dyslipidemia Essential hypertension, benign Microalbuminuria Ischemic Stroke Neuroforaminal stenosis of spine Heart block AV complete (H) Fever, unspecified Coronary artery disease involving native coronary artery of native heart without angina pectoris Hypokalemia Hypomagnesemia Urine incontinence Acute on chronic congestive heart failure, unspecified heart failure type (H) Heart failure, diastolic, acute (H) Pericardial effusion End stage renal disease (H) Anemia in chronic kidney disease Chronic heart failure with preserved ejection fraction (H) Heart block Abdominal pain ACP (advance care planning) Anemia Arteriosclerotic vascular disease ATN (acute tubular necrosis) (H) Depression, major, single episode, mild (H) History of COVID-19 History of stroke Major depressive disorder, recurrent, moderate (H) Hypoglycemia Acute kidney injury (H) Nephrolithiasis NSTEMI (non-ST elevation myocardial infarction) (H) Other hyperlipidemia Other intervertebral disc displacement, lumbar region Palliative care by specialist Perinephric hematoma Posttraumatic stress disorder Severe recurrent major depression without psychotic features (H) Hypertension
- Andere Medikamente
- Acetaminophen TYLENOL 500 MG Take 1,000 mg by mouth daily as needed for pain Albuterol Sulfate ACCUNEB 1.25 MG/3ML Inhale 1 ampule into the lungs every 4 hours as needed for wheezing amLODIPine Besylate NORVASC 5 MG Take 5 mg by mouth 2 t
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 21.10.2021
- Impfdatum
- 20.10.2021
- Beginn
- 20.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Error: Booster Given Too Early-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 15.10.2021
- Impfdatum
- 15.10.2021
- Beginn
- 15.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Interchange of vaccine products
Symptomtext
Patient scheduled for 3 dose of Moderna vaccine which was given by nursing staff. Patient did not present proof of first 2 doses. After administration of Moderna vaccine, it was discovered that first 2 doses were Pfizer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetes mellitus, neuropathy, COPD, hyperlipidemia, cognitive impairment, obesity, Stage 3a chronic kidney disease
- Andere Medikamente
- albuterol inhaler, arformoterol, benadryl, gabapentin, glipizide XL, duoneb, metformin, triamcinolone cream
- Allergien
- aspirin
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 12.10.2021
- Impfdatum
- 23.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Wrong product administered
Symptomtext
Patient came in for 2nd Shingrix shot but was given Moderna Covid shot instead. Pharmacist realized mistake after and patient was then given the Shingrix shot as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 12.10.2021
- Impfdatum
- 26.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amenorrhoea
Dysmenorrhoea
Heavy menstrual bleeding
Intermenstrual bleeding
Menstrual disorder
Symptomtext
Started Spotting (menstrual) the day after i received my vaccine, bled for 1 1/2 days, then i didn't bleed or have a period for 55 days straight, followed by a horrible and really heavy period with bad cramps and heavy bleeding. I am not on any medication or birth control and am always very regular with my cycles.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amenorrhoea
- Hospital-Tage
- -
- Labordaten
- Doctors do not care about menstruation and cant do anything about it besides tell you its "stress" related.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 09.10.2021
- Impfdatum
- 30.08.2021
- Beginn
- 30.08.2021
- 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
On 08/30/2021 Patient came with her mother and father to get get the covid-19 vaccine. after talking to them I gave them forms to fill out and told her she will be getting the Pfizer vaccine. She then said all of them will get Pfizer vaccine. I went and got their Pfizer vaccines ready. I check their cards and dates of birth to make sure. right as I was about to take their vaccines to the room to give them, patient came rushing to let me know that she don't want the pfizer vaccine and that they prefer the Moderna vaccine and they are sorry to have made me prepare the Pfizer vaccine. I said ok , I have other people waiting but l get their vaccines changed from Pfizer to Moderna. I then discarded the Pfizer vaccines i had prepared for them and got moderna vaccines ready. Because of the rush and confussion I totally forgot that patient is 15 years old and cannot take Moderna vaccine untill she's 16years old. After I gave them their Moderna vaccines, they thanked me. on 10/07/2021 she came back for the second does. We couldn't give her the Moderna vaccine again because she is under age. She will get it only when she's 16 years of age.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none, Patient did not suffer any adverse effect.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 09.10.2021
- Impfdatum
- 11.09.2021
- Beginn
- 23.09.2021
- Tage bis Beginn
- 12,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Vertigo
Symptomtext
On the 23rd of September I experienced 2 non-consecutive head spinning bouts that lasted for about 10 minutes or so. Shortly after, a ringing sound started to develop in my right ear and has persisted since the 23rd of September to the current day. The symptoms appear to be parallel to what is experienced with tinnitus - phantom sounds vary from a whooshing, to a high pitched ringing. There has been no break since the onset of the ringing on the 23rd of September.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- I visited clinic on October 1st. The PA-C in charge prescribed a course of antibiotics and steroids. It has been almost 10 days since being on the steroids and antibiotics and the tinnitus has not ceased.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Allegra, Flonase
- Allergien
- Sulfur based medications
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 09.10.2021
- Impfdatum
- 20.07.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 12,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Nerve conduction studies normal
Neuralgia
Symptomtext
Bilateral Nerve pain in both feet present 1-2 weeks after first dose. Still ongoing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nerve conduction studies normal
- Hospital-Tage
- -
- Labordaten
- Podiatrist referred me to a neurologist. Neurologist did a nerve study that came back normal. ordering MRI.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 08.10.2021
- Impfdatum
- 01.08.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- 31,0
- Dosis
- 2
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
Swollen Lymph nodes around ears when exposed to cold wind. Swelling increases gradually over next two days. When Ibuprofen 2 tablets was used about every 8hrs, swelling reduced after about 3-5 days. If exposed to cold again, swelling returns. Cold weather started after about a month after 2nd dose; that when the side affects started. Till dates it started in near one ear and then second with the other ear and then again with first one in a span of about 3 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Levothyroxine 100mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 04.10.2021
- Impfdatum
- 26.07.2021
- Beginn
- 28.09.2021
- Tage bis Beginn
- 64,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
9/28 symptomatic COVID breakthrough. Inpatient admit 10/2/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 18.09.2021
- Impfdatum
- 29.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypersensitivity
Nasal congestion
Oropharyngeal discomfort
Product dose omission issue
Symptomtext
Throat issues; I am having congestion and allergies after receiving the vaccine.; I am having congestion and allergies after receiving the vaccine; Patient does not plan on getting the second dose of the Moderna COVID-19 vaccine.; This spontaneous case was reported by a consumer and describes the occurrence of OROPHARYNGEAL DISCOMFORT (Throat issues), NASAL CONGESTION (I am having congestion and allergies after receiving the vaccine.), HYPERSENSITIVITY (I am having congestion and allergies after receiving the vaccine) and PRODUCT DOSE OMISSION ISSUE (Patient does not plan on getting the second dose of the Moderna COVID-19 vaccine.) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. Concurrent medical conditions included Allergy NOS (history of allergies for too many things including medals and antibiotics.), Allergic reaction to antibiotics and Allergy (Medals). On 29-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced OROPHARYNGEAL DISCOMFORT (Throat issues), NASAL CONGESTION (I am having congestion and allergies after receiving the vaccine.), HYPERSENSITIVITY (I am having congestion and allergies after receiving the vaccine) and PRODUCT DOSE OMISSION ISSUE (Patient does not plan on getting the second dose of the Moderna COVID-19 vaccine.). At the time of the report, OROPHARYNGEAL DISCOMFORT (Throat issues) and NASAL CONGESTION (I am having congestion and allergies after receiving the vaccine.) had not resolved, HYPERSENSITIVITY (I am having congestion and allergies after receiving the vaccine) outcome was unknown and PRODUCT DOSE OMISSION ISSUE (Patient does not plan on getting the second dose of the Moderna COVID-19 vaccine.) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. The Patient reported adverse event kyriad ever since he received the maternal COVID-19 vaccine The patient have allergies too many things including medals and antibiotics. Throat issues previously treated with steroids.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypersensitivity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergic reaction to antibiotics; Allergy (Medals); Allergy NOS (history of allergies for too many things including medals and antibiotics.)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- -
- Geschlecht
- F
- Eingang
- 17.09.2021
- Impfdatum
- 02.09.2021
- Beginn
- 01.09.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Product storage error
Symptomtext
Dose administered more than 12 hours after initial puncture; Vial was punctured on 01-Sep-2021 at 11:05 AM/dose was administered on 02-Sep-2021 at 2:58 PM; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered more than 12 hours after initial puncture) and PRODUCT STORAGE ERROR (Vial was punctured on 01-Sep-2021 at 11:05 AM/dose was administered on 02-Sep-2021 at 2:58 PM) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Sep-2021 at 2:58 PM, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Sep-2021 at 11:05 AM, the patient experienced PRODUCT STORAGE ERROR (Vial was punctured on 01-Sep-2021 at 11:05 AM/dose was administered on 02-Sep-2021 at 2:58 PM). On 02-Sep-2021 at 2:58 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered more than 12 hours after initial puncture). On 02-Sep-2021 at 2:58 PM, EXPIRED PRODUCT ADMINISTERED (Dose administered more than 12 hours after initial puncture) and PRODUCT STORAGE ERROR (Vial was punctured on 01-Sep-2021 at 11:05 AM/dose was administered on 02-Sep-2021 at 2:58 PM) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. Treatment information was not provided. The reporter stated that a pharmacy intern had administered an expired dose to the patient. The vial was initially stored in the fridge on 30-Aug-2021. It did not undergo any previous temperature excursion. The total amount of time spent at room temperature was 20 minutes. Most recent FOLLOW-UP information incorporated above includes: On 07-Sep-2021: Updated correspondence contact box, patient initials and gender. On 07-Sep-2021: Follow up contains no new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 11.09.2021
- Impfdatum
- 02.08.2021
- Beginn
- 23.08.2021
- Tage bis Beginn
- 21,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
They gave a patient his 2nd dose yesterday, 23Aug2021 after giving him his first dose on 2Aug2021; This spontaneous case was reported by a pharmacist and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (They gave a patient his 2nd dose yesterday, 23Aug2021 after giving him his first dose on 2Aug2021) in a 26-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 939902 and 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 23-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 23-Aug-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (They gave a patient his 2nd dose yesterday, 23Aug2021 after giving him his first dose on 2Aug2021). On 23-Aug-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (They gave a patient his 2nd dose yesterday, 23Aug2021 after giving him his first dose on 2Aug2021) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not provided by the reporter. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 07.09.2021
- Impfdatum
- 21.07.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 31,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Pharmacist called to report that they gave a vaccine to two patients that was past the 12hr window; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Pharmacist called to report that they gave a vaccine to two patients that was past the 12hr window) in a 70-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 017E21A and 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 21-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 21-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 21-Aug-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Pharmacist called to report that they gave a vaccine to two patients that was past the 12hr window). On 21-Aug-2021, EXPIRED PRODUCT ADMINISTERED (Pharmacist called to report that they gave a vaccine to two patients that was past the 12hr window) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant medications were provided by the reporter. No Treatment information was reported. Most recent FOLLOW-UP information incorporated above includes: On 23-Aug-2021: Follow up received and contains No New Information. On 25-Aug-2021: Follow up received added patient demographics (patient race), Second dose details(Route and site of administration).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 07.09.2021
- Impfdatum
- 24.07.2021
- Beginn
- 21.08.2021
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Gave a vaccine to two patients that was past the 12hr window; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Gave a vaccine to two patients that was past the 12hr window) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 017E21A and 091D21A) for COVID-19 vaccination. Concurrent medical conditions included Adhesive tape allergy (tape), Allergy to antibiotic (Amoxicillin) and Allergy to antibiotic (Erythromycin). On 24-Jul-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 21-Aug-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to 1 dosage form. On 21-Aug-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Gave a vaccine to two patients that was past the 12hr window). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Gave a vaccine to two patients that was past the 12hr window) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication were provided by the reporter No treatment medication were provided by the reporter Most recent FOLLOW-UP information incorporated above includes: On 23-Aug-2021: Follow up received on 23 Aug 2021 include reporter first name updated. On 25-Aug-2021: Follow up received on 25 Aug 2021 include no new information. On 25-Aug-2021: Follow-up received on 25 Aug 2021 include patient demographics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Adhesive tape allergy (tape); Allergy to antibiotic (Amoxicillin)
- Vorgeschichte
- Medical History/Concurrent Conditions: Allergy to antibiotic (Erythromycin)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 03.09.2021
- Impfdatum
- 01.08.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Unevaluable event
Symptomtext
pt started to feel faint before shot and pt in and out of frozen catatonic state. head started to fall back. called for pharmacist. out for 3 to 5 minutes and felt better and wanted the shot...nothing happened after the shot. this all occurred before the shot due to anxiety and this has happened to the pt before
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- non
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 02.09.2021
- Impfdatum
- 05.08.2021
- Beginn
- 19.08.2021
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deafness unilateral
Symptomtext
Patient stated she lost hearing in 1 ear about 2 weeks after receiving vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deafness unilateral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 01.09.2021
- Impfdatum
- 25.07.2021
- Beginn
- 25.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Patient received the Pfizer vaccine 7/2/21 and the moderna vaccine on 7/25/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknowm
- Vorgeschichte
- unknowm
- Andere Medikamente
- unknown
- Allergien
- nka
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 01.09.2021
- Impfdatum
- 14.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site erythema
Vaccination site swelling
Vaccination site warmth
Symptomtext
injection site warm to touch; Injection site redness; Injection site swollen up; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE WARMTH (injection site warm to touch), VACCINATION SITE ERYTHEMA (Injection site redness) and VACCINATION SITE SWELLING (Injection site swollen up) in a 58-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical history was reported by the reporter. Concomitant products included APIXABAN (ELIQUIS), FLECAINIDE, KETOROLAC TROMETHAMINE (TORADOL), POTASSIUM CHLORIDE, ATORVASTATIN, HYDROCHLOROTHIAZIDE, TRIAMTERENE (TRIAMTERENE/HCTZ) and PREGABALIN for an unknown indication. On 14-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced VACCINATION SITE WARMTH (injection site warm to touch), VACCINATION SITE ERYTHEMA (Injection site redness) and VACCINATION SITE SWELLING (Injection site swollen up). At the time of the report, VACCINATION SITE WARMTH (injection site warm to touch), VACCINATION SITE ERYTHEMA (Injection site redness) and VACCINATION SITE SWELLING (Injection site swollen up) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No Medical history was reported by the reporter
- Andere Medikamente
- ELIQUIS; FLECAINIDE; TORADOL; POTASSIUM CHLORIDE; ATORVASTATIN; TRIAMTERENE/HCTZ; PREGABALIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 02.08.2021
- Beginn
- 12.08.2021
- Tage bis Beginn
- 10,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Symptomtext
Positive for COVID-19 Disease, Minimal COVID-19 Disease symptoms; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (Positive for COVID-19 Disease, Minimal COVID-19 Disease symptoms) in a 35-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 12-Aug-2021, the patient experienced COVID-19 (Positive for COVID-19 Disease, Minimal COVID-19 Disease symptoms). At the time of the report, COVID-19 (Positive for COVID-19 Disease, Minimal COVID-19 Disease symptoms) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 12-Aug-2021, SARS-CoV-2 test: positive (Positive) Positive. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No relevant concomitant products were reported . The patient was treated with OTC drugs at home and did not see a physician. The patient's spouse reported that the pharmacist refused to schedule the second shot and told them that they have to wait 90 days before getting the second dose. Company Comment: Based on the current available information, the mRNA-1273 does not contain a virus capable of causing infection and with the occurrence of COVID-19 infection after vaccination, the causality of this event is assessed as not applicable. Reporter did not allow further contact Most recent FOLLOW-UP information incorporated above includes: On 16-Aug-2021: Significant Follow up received : patient initials added; Sender's Comments: Based on the current available information, the mRNA-1273 does not contain a virus capable of causing infection and with the occurrence of COVID-19 infection after vaccination, the causality of this event is assessed as not applicable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20210812; Test Name: COVID virus test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- -
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 09.07.2021
- Beginn
- 01.07.2021
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Somnolence
Symptomtext
a little sleepiness; This spontaneous case was reported by a consumer and describes the occurrence of SOMNOLENCE (a little sleepiness) in a 25-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 091D21A and 88221S) 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) (Intramuscular) dosage was changed to 1 dosage form. In July 2021, the patient experienced SOMNOLENCE (a little sleepiness). At the time of the report, SOMNOLENCE (a little sleepiness) outcome was unknown. mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosing remained unchanged. Concomitant medications were not provided. Treatment information was not reported. This case was linked to MOD-2021-283007 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Somnolence
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 28.08.2021
- Impfdatum
- 04.08.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
patient received 2 different manufactured doses of covid19 vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of INTERCHANGE OF VACCINE PRODUCTS (patient received 2 different manufactured doses of covid19 vaccine) in a 49-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 091D21A) for COVID-19 vaccination. Co-suspect product included non-company product COVID-19 VACCINE NRVV AD (CHADOX1 NCOV-19) (COVID-19 VACCINE ASTRAZENECA) for COVID-19 vaccination. No Medical History information was reported. On 04-Aug-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient started COVID-19 VACCINE NRVV AD (CHADOX1 NCOV-19) (COVID-19 VACCINE ASTRAZENECA) (unknown route) at an unspecified dose. On an unknown date, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (patient received 2 different manufactured doses of covid19 vaccine). At the time of the report, INTERCHANGE OF VACCINE PRODUCTS (patient received 2 different manufactured doses of covid19 vaccine) had resolved. 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 Treatment medications were provided No Concomitant medications were provided Most recent FOLLOW-UP information incorporated above includes: On 12-Aug-2021: Follow up received contains Non Significant Information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 27.08.2021
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
NO ADVERSE EVENTS TO REPORT. REPORTING THAT DOSE WAS GIVEN TO CHILD UNDER THE APPORVED AGE LIMIT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 27.08.2021
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No negative side effects to report. Only reporting that dose was administered to a child under the approved age limit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 27.08.2021
- Impfdatum
- 27.07.2021
- Beginn
- 27.07.2021
- 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 reported no ill effects from the vaccine. Report is being completed only because it was administered to a child under the approved age limit.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 26.08.2021
- Impfdatum
- 24.07.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No adverse reaction was noted Pt was administered vaccine & he's 17 years old.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NONe
- Allergien
- NO
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 26.08.2021
- Impfdatum
- 26.07.2021
- Beginn
- 26.07.2021
- 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
Administration error: Mother of the minor comes to the center Mall asking which is the vaccine for underage. They answer PFIZER. Mother reports her son was vaccinated with MODERNA with his first dose. Staff member notifies the nurse in charge and to the director. They collaborate with the mother's allegation and Doctor advices the mother to wait for the vaccine to be approve for 18 year old patients. Nurse who vaccinated the minor is not working in the vaccination center. All staff is reoriented about indications and risk of vaccines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NKDA
- Vorgeschichte
- NKDA
- Andere Medikamente
- NONE MEDICATION
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 26.08.2021
- Impfdatum
- 04.08.2021
- Beginn
- 04.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hormone level abnormal
Uterine leiomyoma
Symptomtext
Patient female 36 years of age, oriented in time, place, date. Reports that after getting the second vaccine dose MODERNA "felt rush" (accelerated). Patient reports that it could be anxiety and that her last meal was at 2pm (a snack) and also started her period today. She has Uterine fibroid. 4:09 pm verbalizes feeling better. Patient is moved to take vitals B/P: 130/90, pulse 93, O2 99%, glucose 99%. Patient is recommended to monitor symptoms, and to visit her doctor if they worsen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hormone level abnormal
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 24.08.2021
- Impfdatum
- 31.07.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anosmia
Symptomtext
Patient stated that he had permanently lost sense of smell after the second dose. Stated he started the day after and has not returned. Denied that he has or had covid. Advised patient to seek medical care from primary care doctor, but stated he does not have primary care doctor and was not going to seek any additional care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anosmia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- dermatologic disorders
- Vorgeschichte
- unknown
- Andere Medikamente
- buprenorphine, pregabalin, clonazepam
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 22.08.2021
- Impfdatum
- 10.08.2021
- Beginn
- 11.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Electrocardiogram
Full blood count
Hyperhidrosis
Magnetic resonance imaging head
Metabolic function test
Vision blurred
Visual field defect
Visual impairment
Symptomtext
I got awake ~12:15 am on 8/11/21, felt sweaty, took off the blanket. Checked my phone for messages. Could not make out anything on the screen. Put on my reading glasses, still could not make out anything on the screen. Objects in the distance appeared blurry, could make out silhouettes but not detail. Both eyes had blurred vision, left eye had no peripheral vision, both eyes had "spider webs". Got up to wash my face in case that would clear the disturbance; it did not. Called a neighbor to take me to the hospital E.R. Arrived there around 1:15 a.m.. By then the vision was mostly returned but still not my normal.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electrocardiogram
- Hospital-Tage
- -
- Labordaten
- CBC with Differential Comprehensive Metabolic Panel EKG 12-Lead MRI Brain w/o contrast The first three of the above were normal. The MRI was consistent with the last one done in 2010, no changes from 2010.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diagnosed as possible M.S. in the year 2000, no limiting conditions, not on any medicine for it
- Andere Medikamente
- Doxycycline 50 mg, Multi-vitamin, Fish oil capsule, Vitamin C, Vitamin D3
- Allergien
- Rhus Tox Antigen (poison ivy preventative injection)
- Vorherige Impfungen
- Anaphylaxis as a teenager, from Rhus Tox Antigen injection, approx. 1977?
- Staat
- PR
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 19.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
ADMINISTRATION ERROR: NURSE ADMINISTERED FIRST DOSE OF MODERNA LOT #091D21A ON LEFT ARM TO A 13 YRS OLD. INSTEAD OF ADMINISTERING DOSE OF PFIZER WHICH IS INDICATED FOR THE AGE OF THE PATIENT TO THE AUTHORIZATION FOR EMERGENCY USE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- NO LABORATORY TEST ARE PERFORMED YET.
- Aktuelle Erkrankungen
- NKDA
- Vorgeschichte
- NKDA
- Andere Medikamente
- DOES NOT TAKE MEDICATIONS
- Allergien
- REPORTS HAVING NO ALLERGIES
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 16.08.2021
- Impfdatum
- 16.08.2021
- Beginn
- 16.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Eye haemorrhage
Eye injury
Fall
Symptomtext
Patient fell off from an armrest chair while waiting after his second Moderna shot. It happened so suddenly after about 5 minutes waiting on the chair. His left eye brown had a cut and was bleed. He was under quick care of the facility employees and then paramedics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye haemorrhage
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- ADHD
- Andere Medikamente
- Adderall
- Allergien
- Onion and garlic
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 15.08.2021
- Impfdatum
- 14.08.2021
- Beginn
- 14.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dry mouth
Dysphagia
Lip swelling
Symptomtext
Patient reports experiencing lip swelling and a "lump sensation" in right side of throat around 30 minutes after vaccination up to around 2-2.5 hours after vaccination, as well as dry mouth/difficulty swallowing. Did not experience difficulty breathing and these symptoms had not recurred by time of report over 24 hours later (around 2:30 PM the next day) to the pharmacy. Patient was advised to call 911 if these symptoms returned or if she developed difficulty breathing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dry mouth
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- ACE-Inhibitors, Blue Dye, CCBs, Cephalosporins, Macrolides, NSAIDs, Penicillins
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 14.08.2021
- Impfdatum
- 29.07.2021
- Beginn
- 29.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect product formulation administered
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect product formulation administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 14.08.2021
- Impfdatum
- 29.07.2021
- Beginn
- 29.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 13.08.2021
- Impfdatum
- 13.08.2021
- Beginn
- 13.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
MAKING THIS REPORT BECAUSE THE PATIENT HAD THE INITIAL VACCINATION IN JANUARY 2021 AND IS NOW RECEIVING THE 2ND VACCINATION IN AUGUST 2021.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- na
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 09.08.2021
- Impfdatum
- 07.08.2021
- Beginn
- 07.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Hypoaesthesia
Limb discomfort
Symptomtext
Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Weakness-Medium, Additional Details: He stated that his left arm went numb (the arm that he received the injection in) and that it then felt heavy. He told me this 15 minutes after he had received the vaccination. I did give him the pharmacy phone number if he had any further issues, he did not call the next day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 07.08.2021
- Impfdatum
- 30.07.2021
- Beginn
- 30.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient request Covid Vaccine on 7/30/2021 got a Moderna dose but did not mention got a previous Pfizer dose at other non pharmacy location on 6/5/2021. Pharmacy screening protocol was followed which asked if got any vaccine on the prior eight weeks and he answered "no" . Patient said he is doing fine, no other symptoms related to the incident.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- Hep C
- Vorgeschichte
- Liver Desease
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 06.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
patient received vaccine 7 days prior to due date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- hypertension
- Vorgeschichte
- hypertension
- Andere Medikamente
- metoprolol succinate 100mg
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 06.08.2021
- Impfdatum
- 06.08.2021
- Beginn
- 06.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Contusion
Fall
Injury
Symptomtext
PT FELL TO THE FLOOR UPON WALKING OUT OF THE CONSULTATION ROOM. PATIENT WAS CONSCIOUS, EYES WERE ALERT, AND KNEW WHERE HE WAS. HE HAD VISIBLE BRUISING ON HIS SIDE WHERE HE HIT HIMSELF. 911 WAS CALLED AND PATIENT WAS ASSESSED BY THEM AND TAKEN BY AMBULANCE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Contusion
- Hospital-Tage
- -
- Labordaten
- UNKNOWN BY PHARMACY.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HEMOPHILIA
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 04.08.2021
- Impfdatum
- 31.07.2021
- Beginn
- 01.08.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Staphylococcal infection
Symptomtext
Pt reported is currently being treated for a staph infection in the injection arm. was started on bactrim ds 08/03/21
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Staphylococcal infection
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- chronic pain from small fiber neuralgia
- Andere Medikamente
- gabapentin
- Allergien
- Sumatriptan
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 03.08.2021
- Impfdatum
- 03.08.2021
- Beginn
- 03.08.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Jaw clicking
Symptomtext
Patient reports jaw clicking 2 minutes after receiving the vaccine. She says the popping feeling never stopped. She does report having dental surgery 13 days ago but does not believe it is related. She will monitor and call her dentist if it continues for more than 2 days. She said she does "self-lymph drainage" regularly too.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Jaw clicking
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- had dental procedure done 2 weeks ago
- Vorgeschichte
- asthma
- Andere Medikamente
- -
- Allergien
- sulfa, keflex
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 02.08.2021
- Impfdatum
- 23.07.2021
- Beginn
- 30.07.2021
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
Swollen gland in armpit of left arm (injection arm)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- Hydrocodone 5-325 mg 1 tablet 2 - 3 times daily Cyclobenzaprine 10 mg 2 tablet daily ( 1 am, 1 pm) Fish oil 2400 mg daily Zinc 50 mg daily Vitamin C 500 mg daily
- Allergien
- Cocaine, anything latex. Also allergic to grass, dirt, dust,
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 30.07.2021
- Impfdatum
- 28.07.2021
- Beginn
- 28.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product storage error
Symptomtext
Patient received a vaccine that was outside of recommended storage. Vaccine expired at 8:30 pm on the 27th and vaccine was given at 11:43 am on the 28th. Moderna was contacted and stated the patient should watch for signs of infection at the site. Patient called and did not have a reaction at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unkown
- Vorgeschichte
- none reported
- Andere Medikamente
- unknown
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 30.07.2021
- Impfdatum
- 28.07.2021
- Beginn
- 28.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Product storage error
Symptomtext
Patient received a vaccine that was outside of recommended storage. Vaccine expired at 8:30 pm on the 27th and vaccine was given at 11:43 am on the 28th. Moderna was contacted and stated the patient should watch for signs of infection at the site. Patient called and did not have a reaction at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- NONE
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 27.07.2021
- Impfdatum
- 18.07.2021
- Beginn
- 18.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Hypoaesthesia oral
Symptomtext
Tongue numbess, burned sensation -- immediate onset after 2nd injection. Symptoms remain the same after 9 days post vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Burning sensation
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- Tretinoin
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 25.07.2021
- Impfdatum
- 24.07.2021
- Beginn
- 24.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood glucose normal
Fall
Flushing
Symptomtext
Patient received the 1st dose of Moderna vaccine at 5:30PM. Patient was advised to wait for 15 minutes and report to the pharmacy team know if there was any unusual reaction. At 5:40PM , patient informed that he was feeling flushy and he fell down immediately on the floor. I instructed my technician to call 911 immediately. He woke up 30 seconds after falling down and I was there to check on him. We observed him and offered a bottle of water. The 911 team arrived and did a few tests: measured blood pressure reading, collected the heart rate reading, performed the EKG and glucose test. After 20 minutes, patient was alert. He was able to provide answers from the 911 team correctly (his address, the city that he was from, the city that he was at, his full name) and informed that he was okay to go home. The 911 advised him to have a few sips of Pedialyte and had a small snack. Patient reported that he had not eaten since the morning and had very few liquid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood glucose normal
- Hospital-Tage
- -
- Labordaten
- 1st reading - The blood pressure reading (left arm): 148/123, Heart rate: 59. 2nd reading - The blood pressure reading (left arm): 139/106, Heart rate: 54. The blood pressure reading (right arm): 97/156. Blood glucose: 114. The EKG reading was normal.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 23.07.2021
- Impfdatum
- 23.07.2021
- Beginn
- 23.07.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Pallor
Symptomtext
Patient complained about feeling weak. Turned pale however recovered upon fluid uptake and reassessment. Blood pressure check attempted, no result due to machine malfunction. Called 911 while patient pale. Patient provided with bottle of water and orange juice. Upon interview, patient has not had any breakfast.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- vaccination (already mentioned)
- Aktuelle Erkrankungen
- anxiety
- Vorgeschichte
- anxiety
- Andere Medikamente
- unknown
- Allergien
- n/a
- Vorherige Impfungen
- -