VAERS Reports 068H21A

VAERS 2670125

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: -
Alter: 56,0
Geschlecht: F
Eingang: 11.08.2023
Impfdatum: 27.12.2021
Beginn: 06.07.2022
Tage bis Beginn: 191,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute myocardial infarction

Symptomtext

ACUTE NON ST ELEVATION MI

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Praegender Schweregrund: Acute myocardial infarction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2668609

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 09.08.2023
Impfdatum: 13.01.2022
Beginn: 06.02.2023
Tage bis Beginn: 389,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Cerebral artery occlusion Cerebrovascular accident Symptom recurrence

Symptomtext

ACUTE STROKE DUE TO OCCLUSION OF LEFT MIDDLE CEREBRAL ARTERY ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY ACUTE HYPOXEMIC RESPIRATORY FAILURE 1/24/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2666994

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 07.08.2023
Impfdatum: 17.02.2022
Beginn: 15.01.2023
Tage bis Beginn: 332,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute respiratory failure Hypoxia Neuropathy peripheral

Symptomtext

PERIPHERAL NEUROPATHY ACUTE RESPIRATORY FAILURE ACUTE HYPOXEMIC RESPIRATORY FAILURE HYPOXIA

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2636248

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: -
Alter: 84,0
Geschlecht: F
Eingang: 24.05.2023
Impfdatum: 24.01.2022
Beginn: 08.08.2022
Tage bis Beginn: 196,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Acute respiratory failure Aortic arteriosclerosis Bronchitis COVID-19 Chronic respiratory failure Ischaemic stroke Peripheral embolism Peripheral ischaemia Respiratory failure

Symptomtext

I63.9 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 8/8/2022 EMBOLISM OF LEFT ARM ARTERY J96.00 ACUTE RESPIRATORY FAILURE 10/26/2022 EMBOLISM OF LEFT ARM ARTERY J96.11 CHRONIC HYPOXEMIC RESPIRATORY FAILURE 1/11/2023 EMBOLISM OF LEFT ARM ARTERY I63.9 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 8/8/2022 LEFT LEG ISCHEMIA J96.00 ACUTE RESPIRATORY FAILURE 10/26/2022 LEFT LEG ISCHEMIA J96.11 CHRONIC HYPOXEMIC RESPIRATORY FAILURE 1/11/2023 LEFT LEG ISCHEMIA I63.9 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 8/8/2022 HX OF ARTERIAL THROMBOSIS J96.00 ACUTE RESPIRATORY FAILURE 10/26/2022 HX OF ARTERIAL THROMBOSIS J96.11 CHRONIC HYPOXEMIC RESPIRATORY FAILURE 1/11/2023 HX OF ARTERIAL THROMBOSIS I63.9 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 8/8/2022 COVID-19 ACUTE BRONCHITIS J96.00 ACUTE RESPIRATORY FAILURE 10/26/2022 COVID-19 ACUTE BRONCHITIS J96.11 CHRONIC HYPOXEMIC RESPIRATORY FAILURE 1/11/2023 COVID-19 ACUTE BRONCHITIS I63.9 ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY 8/8/2022 ATHEROSCLEROSIS OF AORTA J96.00 ACUTE RESPIRATORY FAILURE 10/26/2022 ATHEROSCLEROSIS OF AORTA J96.11 CHRONIC HYPOXEMIC RESPIRATORY FAILURE 1/11/2023 ATHEROSCLEROSIS OF AORTA

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2628992

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: -
Alter: 62,0
Geschlecht: F
Eingang: 09.05.2023
Impfdatum: 02.02.2022
Beginn: 21.09.2022
Tage bis Beginn: 231,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Cerebrovascular accident Hypotension Transient ischaemic attack

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE TRANSIENT CEREBRAL ISCHEMIA ACUTE STROKE, UNSPECIFIED TYPE AND ARTERY HYPOTENSION

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Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2617650

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A-

kritisch

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 19.04.2023
Impfdatum: 28.12.2021
Beginn: 12.01.2022
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Idiopathic generalised epilepsy Pulmonary embolism Status epilepticus

Symptomtext

EPILEPSY, GENERALIZED IDIOPATHIC STATUS EPILEPTICUS EPILEPSY, UNSPECIFIED PULMONARY EMBOLISM, UNSPECIFIED. PATIENT HAD SAME ADVERSE EVENT ON : 02/25/2022, 04/09/2022, 04/12/2022, 04/21/2022, 04/22/2022, AND 5/17/2022

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2586343

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: KY
Alter: 56,0
Geschlecht: M
Eingang: 23.02.2023
Impfdatum: 21.10.2022
Beginn: 22.12.2022
Tage bis Beginn: 62,0
Dosis: 3
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Death

Symptomtext

PATIENT EXPIRED ON 12/22/2022

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: COPD COAL WORKER PNEUMOCONIOSIS
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 2581535

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: WA
Alter: 69,0
Geschlecht: M
Eingang: 14.02.2023
Impfdatum: 24.01.2022
Beginn: 29.01.2022
Tage bis Beginn: 5,0
Dosis: UNK
Route/Site: UN / UN

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac arrest Hypoxic-ischaemic encephalopathy Subarachnoid haemorrhage

Symptomtext

Cardiac Arrest Spontaneous Subarachnoid Hemorrhage Possible Cerebral Aneurysm Hypoxic-Ischemic Encephalopathy

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2551301

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 05.01.2023
Impfdatum: 12.01.2022
Beginn: 27.11.2022
Tage bis Beginn: 319,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Abdominal tenderness Acute respiratory failure Angiogram pulmonary normal Aspiration Asthenia Barium swallow abnormal Blood creatine phosphokinase increased Blood culture negative COVID-19 Cerebral atrophy Cerebral ventricle dilatation Computerised tomogram abdomen normal Computerised tomogram head abnormal Computerised tomogram thorax normal Condition aggravated Confusional state Constipation Culture urine negative

Symptomtext

Acute respiratory failure with hypoxia--Resolved Aspiration pneumonia COVID -19 Virus infection -Developed acute decompensation on 12/2 following aspiration event -CTPA negative for PE -Positive test at RMH 11/27/22 -O2 demand improving, weaned off of HHF and now on LFNC intermittently -completed Decadron 12/8 -Completed remdesivir 12/5 -Completed antibiotic therapy with Vanc/Cefepime/Unasyn Weakness/Fall UE Tremor Confusion -Presented to the ED from home with worsening confusion, generalized weakness, shuffling gait, UE tremor, and mechanical falls -Etiology uncertain, possible acute illness (COVID), meds (depakote), possible NPH -CTH on admission with dilated ventricles, most likely d/t cerebral volume loss but possible NPH -MRI brain showing mild ventriculomegaly should be closely clinically correlated to exclude NPH. -Neuro Dr consulted and rec possible dc depakote but defer to OP neurologist; possible NPH eval once recovers from illness -Outpatient Movement Disorders referral and neurology department will arrange -MRI C-spine showing neuroforaminal stenosis, recommended following up with Dr. in 6 weeks Metabolic encephalopathy related to infection, resolved -noted since admission. Possible underlying neurological condition, with superimposed metabolic encephalopathy 2/2 covid 19 infection -supportive care, meds as above Leukocytosis, resolved -Patient with increasing WBCs, recently completed IV steroids on 12/8. WBC increased to 32, now 7.82. -No signs of diarrhea to indicate C. Difficile -sputum cx 12/4 neg. Blood cx 12/2 and 12/10 neg. Neg MRSA swab -CT chest, abd and pelvis 12/11 neg for obvious infection -will hold on further antibiotics given no indication of infection. -UA and urine cx negative Rhabdomyolysis, resolved -CPK noted to be >6K on admission, possibly in setting of fall, acute illness -Resolved Malnutrition Dysphagia -Patient with dysphagia and signs of ongoing aspiration. SLP following -Pt had NG, removed 12/10 due to coiling. Repeat MBS 12/13 and failed. New Corflo placed 12/14 and back on tube feeding -Repeat MBS on the 20th still with persistent aspiration risk. - Discussed with patient and spouse, PEG placed 12/22 -Continue speech therapy and tube feeds on discharge Essential Hypertension - Noted, was previously on Losartan 100mg daily. - Orthostatics positive on 12/20, holding for now. - Orthostatics improved 12/21. - Will continue to titrate as necessary. CAD -Per history, continue aspirin and statin Diabetes Mellitus, Type 2 -Hold metformin, cont SS. Controlled. Bipolar Disorder -home meds: Depakote 1000 mg bid. Seroquel 3 tabs(75 mg) q hs. Meds currently reduced due to lethargy-now on Depakote 250mg nightly, Seroquel 25mg nightly. Behavioral med followed. Left sided abdominal tenderness Constipation -ongoing for a few days since PEG tube placement near site of PEG tube -PEG tube in appropriate position with small amount of dried blood, no clinical suggestion of infection -abdominal x ray 12/26 showing large stool load in colon, with PEG tube in position -suppository x1, continue bowel regimen

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 29,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2538459

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: IN
Alter: 39,0
Geschlecht: M
Eingang: 20.12.2022
Impfdatum: 23.12.2021
Beginn: 05.01.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: SYR / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cardiac arrest Death

Symptomtext

Sudden cardiac arrest resulting in death

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Praegender Schweregrund: Cardiac arrest
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: Obesity Pre-HTN
Andere Medikamente: Meclizine prn for vertigo Excedrine prn for migraines
Allergien: none
Vorherige Impfungen: -

VAERS 2473295

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 10.10.2022
Impfdatum: 23.12.2021
Beginn: 03.10.2022
Tage bis Beginn: 284,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute respiratory failure Arthralgia COVID-19 Device malfunction Osteoarthritis X-ray of pelvis and hip abnormal

Symptomtext

Discharge Provider: DO Primary Care Provider: DO Admission Date: 10/3/2022 Discharge Date: Oct 5, 2022 PRESENTING PROBLEM: AICD lead malfunction COVID-19 HOSPITAL COURSE: Patient is a 69-year-old female with past medical history of chronic combined systolic and diastolic congestive heart failure with reduced EF of 22%, nonischemic cardiomyopathy, primary prevention single-chamber AICD placement in 2014 presented to the ER with a chief complaint of right hip pain. Patient has had pain resolved with some IV Tylenol in the ER but was noted to have COVID-19. No overt hip pathology were noted on workup, x-ray was suggestive of mild degenerative osteoarthritic changes of the right hip. In the ER she was also found to have RV lead fracture. EP was consulted for input. In the ER patient also required 2 L of supplemental oxygen and given impending further medical workup, admission was recommended. Patient was transferred from ER to hospital for EP evaluation. On arrival to our facility, patient was treated for acute hypoxic respiratory failure secondary likely COVID-19 and electrophysiology was consulted for RV lead fracture evaluation. In regards to COVID-19, patient received 2 doses of Decadron. The patient was noted to not require any supplemental oxygen during the morning but does need supplemental oxygen at night which is suggestive of likely underlying obstructive sleep apnea. Patient was supposed to be using CPAP at night but does not have her device during the hospital stay. Electrophysiology evaluated the patient and fitted her for a life vest. Plan is to follow-up with her outpatient to address the limb lead fracture. Given significant underlying heart failure, a structural heart evaluation was recommended and outpatient consult ordered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Heart Failure with reduced EF (Advanced heart failure clinic) Medical non-compliance ICD (implantable cardioverter-defibrillator) in place NICM (nonischemic cardiomyopathy) (HCC) Essential hypertension Dyslipidemia Frequent PVCs Type 2 diabetes mellitus with diabetic neuropathy, without long-term current use of insulin (HCC) Obesity (BMI 30-39.9) Type 2 diabetes mellitus without ophthalmic manifestations (HCC) Senile nuclear cataract, bilateral Hyperopia of both eyes COVID-19 Implanted defibrillator electrode lead fracture Pulmonary embolus (HCC)
Andere Medikamente: albuterol HFA (PROVENTIL HFA, VENTOLIN HFA, PROAIR HFA) 108 (90 Base) MCG/ACT inhaler amiodarone (PACERONE) 200 MG tablet aspirin EC 81 MG EC tablet atorvastatin (LIPITOR) 40 MG tablet benzonatate (TESSALON) 100 MG capsule bumetanide (BUMEX
Allergien: None
Vorherige Impfungen: -

VAERS 2370287

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 14.07.2022
Impfdatum: 08.01.2021
Beginn: 14.02.2022
Tage bis Beginn: 402,0
Dosis: 3
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

COVID-19 Death

Symptomtext

Narrative: PATIENT PASSED AWAY DUE TO COVID 19 .HE HAD RECEIVED COVID-19 VACCINE

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2280822

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: KS
Alter: 53,0
Geschlecht: M
Eingang: 17.05.2022
Impfdatum: 23.03.2021
Beginn: 28.04.2021
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: ja Erholt: nein

Angiogram Arthralgia Blood test Cognitive disorder Confusional state Ear discomfort Ear pain Feeling abnormal Headache Laboratory test Magnetic resonance imaging Myocardial infarction Ocular discomfort Photophobia Rhinorrhoea Tinnitus Venogram

Symptomtext

Heart Attack(03/28/2021), Cognitive issues started soon after that, Severe headaches (TAC-PH) started after dose #3, Still having cognitive issues (Executive Disfunction), and daily (all-day)headaches, confusion, brain fog, Tinnitus, Bright light sensitivity, R-Ear Pressure and pain, R-Eye Pressure, Right Nostril runny nose, Joint Pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocardial infarction
Hospital-Tage: 5,0
Labordaten: MRI, MRV, MRA, Cognitive testing, Cognitive re-testing, Blood Tests, Eye Test, throughout 2021 & 2022
Aktuelle Erkrankungen: Depression, PTSD, Chronic Pain
Vorgeschichte: Heart Disease, Depression, PTSD, Chronic Pain
Andere Medikamente: Aspirin BUPROPION HCL ER BUSPIRONE HCL Ezetimibe Tabs Losartan Tabs Metoprolol Succ Er Tabs MODAFINIL Rosuvastatin Tabs SERTRALINE HCL
Allergien: Atorvistatin
Vorherige Impfungen: -

VAERS 2225842

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: -
Alter: 63,0
Geschlecht: M
Eingang: 11.04.2022
Impfdatum: 28.12.2021
Beginn: 18.01.2022
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: unbekannt

Abdominal distension Acute respiratory failure Glycosylated haemoglobin increased Haemoglobin normal Oesophagogastroduodenoscopy Peripheral swelling Polyuria Scrotal cellulitis Scrotal swelling

Symptomtext

Acute respiratory failure with hypoxia - Cardiology was brought on board and patient was started on diuresis and planned for cardiomyopathy work-up. RHC and LHC were scheduled for 01/24 after patient was adequately diuresed. He had resolution of his bilateral leg swelling, abdominal and scrotal swellings. GI was consulted and EGD was doneHemoglobin remained stable and patient continued to improve and was weaned off O2 supplementation He completed IV Zosyn for scrotal cellulitis. ID involvement well appreciated. Per GI recommendation, he is to continue pantoprazole 40 mg twice daily for 3 months. He will follow-up with cardiology outpatient for evaluation for LHC. In the meantime he will continue on 2 mg Bumex p.o. daily Due to HbA1c of 12.3 (greater than 10) he will be discharged on insulin Lantus. He will continue on his home dose of Metformin. ED visit to hospital admission within 6 weeks of receiving the COVID vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 12,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2191843

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: -
Alter: 54,0
Geschlecht: M
Eingang: 11.03.2022
Impfdatum: 15.01.2022
Beginn: 06.02.2022
Tage bis Beginn: 22,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Cerebrovascular accident

Symptomtext

Narrative: Patient received the J&J covid vaccine on 4/2/21. He then got the Moderna vaccine 1/15/22. He presented to the ER with a stroke on 2/6/22. He has a history of prior CVAs in 2010 and 2015 and has been on rivaroxaban 20mg po daily since 1/10/20 (previously on warfarin before that since 3/2015).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2201251

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: -
Alter: 91,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 29.12.2021
Beginn: 16.01.2022
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Death

Symptomtext

Narrative: 90yo male patient with a h/o COPD, RUL lung nodule, and CAD s/p 4V CABG in 2002 transferred from inpatient care to rehab center on 1/8/2022. Facility was informed pt had died on 1/16/2022, cause of death unknown. Pt had received covid vaccines on 1/13/21, 2/12/21, 12/29/21. This death is likely not related to the vaccinations due to patient's comorbidities, advanced age, and length of time from vaccine administration. PROBLEM LAST MOD PROVIDER Seen by palliative care service (SCT 441874000) 12/29/2021 (ICD-10-CM Z51.5) Solitary nodule of lung (SCT 427359005) 03/10/2021 (ICD-10-CM R91.1) History of cholecystectomy (SCT 428882003) 03/13/2018 (ICD-10-CM R69.) Lap chole- CMH 3/1/2018 Abnormal findings on diagnostic imaging of lung 07/29/2016 (SCT 274533004) (ICD-10-CM R91.8) (ICD-9-CM 195.0); FACE 10/08/2008 (ICD-9-CM V43.64); Hip Joint replacement Status 12/13/2007 (Prosthetic or Artificial Device) (ICD-9-CM V43.64) (ICD-9-CM 820.8); Fracture, Femoral Neck 09/13/2007 (ICD-9-CM 719.45); Pain in joint involving 06/15/2007 pelvic region and thigh (ICD-9-CM 719.45) (ICD-10-CM J44.9); Chronic obstructive lung 01/10/2016 disease (CT 13645005) (ICD-9-CM 333.99); Restless Legs * (ICD-9-CM 05/22/2006 333.99) (ICD-9-CM M54.50); Back pain (CT 12/01/2021 161891005) Bruit (ICD-9-CM 785.9) 08/25/2008 1. Carotid , 1, 16-49% stenosis 12/04. neg r 2. Carotids with no sig stenosis 1/07 Postsurgical Aortocoronary Bypass Status (SCT 12/01/2021 399261000) (ICD-10-CM I25.810) 11/02 Old Myocardial Infarction (ICD-9-CM 412.) 04/19/2004 W Inf mi 11/02 Prostate Cancer (SCT 254900004) (ICD-10-CM 06/13/2018 D07.5) Dx 11/01, gleason 8, seeds, xrt, viadur Health Maintenance (ICD-9-CM V65.9) 02/02/2016 1. Pneumovax 6/03 & 11/2012 2. Td 6/03 3. Fobt neg x 3 11/04 4. Colonoscopy 7/07, f/u 10 yrs 5. Tdap 6/13 6.Prevnar 13 7/2015 (ICD-10-CM E78.5); Hyperlipidemia (CT 01/10/2016 55822004) Tobacco Use Disorder (ICD-9-CM 305.1) 04/27/2005 (ICD-10-CM I25.9); Ischemic heart disease 01/10/2016 (CT 414545008) (ICD-9-CM 278.00); OBESITY, UNSP 06/09/2003

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2215727

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: -
Alter: 86,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: -
Beginn: 12.01.2022
Tage bis Beginn: -
Dosis: 2
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Acute respiratory failure Cardiac arrest Death Inappropriate schedule of product administration Pneumonia SARS-CoV-2 test negative

Symptomtext

Narrative: 85 yo mail patient died on 1/12/2022 during inpatient admission. Death was caused by: Cardiac arrest secondary to acute hypoxic respiratory failure secondary to pneumonia (covid negative). Pt had received covid vaccines on 2/23/2021 & 12/23/2021. This death is not related to covid vaccines. Pt's Medical Hx: HTN, T2DM, CAD s/p PCI, obesity, TIA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2202358

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: -
Alter: 95,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 22.12.2021
Beginn: 15.01.2022
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: IM / LA

Tod: ja Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Acute myeloid leukaemia Death

Symptomtext

Narrative: 94 yo male died during inpatient hospice admission. Death was caused by: Acute myeloid leukemia. Pt had received covid vaccines on 1/13/21, 2/10/21, & 12/22/20. This death was not caused by covid vaccines.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2058608

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: MN
Alter: 66,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 27.12.2021
Beginn: 14.01.2022
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / RA

Tod: ja Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Acute respiratory distress syndrome Aspiration Asthenia Blood creatinine increased Blood gases normal COVID-19 Chest X-ray abnormal Chronic respiratory disease Death Decreased appetite Diarrhoea Dyspnoea Endotracheal intubation Extubation Haemoglobin decreased Haemoptysis Hypercapnia Hypoxia

Symptomtext

66-year-old male with a past medical history of interstitial lung disease on chronic prednisone, recurrent DVT/PE on Coumadin, hypertension, diabetes, pulmonary hypertension, OSA on CPAP, obesity who was brought to the ED by EMS for shortness of breath and hypoxia. Patient states that he has not been feeling well for about 3-10 days. On 1/4, he notes that he was unable to sleep that night. Over the last 3 days, he has had diarrhea (watery stools), generalized weakness, poor appetite. He also thinks that he may have gotten more short of breath. He has a chronic dry cough which is at baseline. He went to an outpatient clinic today and was found to be hypoxic to 75%. He appeared to be in acute respiratory distress speaking in 2-3 word sentences. Patient was placed on supplemental 10 L/min of oxygen with improvement in his oxygen saturation to 89%. EMS was called and he was brought to the ED. In the ED, he was requiring 10 L/min of oxygen to maintain saturation in the low 90s. Patient tachycardic to low 100s. Afebrile. Labs are significant for hemoglobin of 12.5, INR 4.0. Creatinine was elevated at 1.41. VBG was unremarkable. A chest x-ray revealed multiple airspace opacities throughout both lungs, worse in the mid and lower lungs. Likely acute bilateral pneumonia superimposed upon chronic lung disease. Patient notes that he has not used his nebulizers for a couple of days. He denies fevers, loss of smell or taste. No vomiting. HOSPITAL COURSE: Admitted January 14 with 9 days of respiratory symptoms. He was COVID positive on the 14th. Due to symptom duration he was not a candidate for tocilizumab. He was treated with IV steroids despite that his respiratory status worsened and he was intubated early January 18. Post intubation he was extremely tenuous with profound hypoxic hypercarbic respiratory failure. This was thought to due to both COVID and also aspiration of blood. Post intubation he had diffuse hemoptysis this is thought due to anticoagulation in the setting of COVID On top of critical respiratory function he was also in septic shock on 4 pressors. He had deteriorating kidney function throughout the day with worsening metabolic acidosis needing a bicarb drip to buffer. In this context we did discuss with his brother that patient is unlikely to survive and he was transitioned to comfort cares. He was extubated January 18 in the afternoon and passed soon after

Weitere VAERSDATA-Felder

Praegender Schweregrund: Death
Hospital-Tage: 4,0
Labordaten: COVID PCR POSITIVE 1/14/2022
Aktuelle Erkrankungen: -
Vorgeschichte: 66-year-old male with a past medical history of interstitial lung disease on chronic prednisone, recurrent DVT/PE on Coumadin, hypertension, diabetes, pulmonary hypertension, OSA on CPAP, obesity
Andere Medikamente: -
Allergien: NO KNOWN
Vorherige Impfungen: -

VAERS 2010337

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

kritisch

Staat: KY
Alter: 25,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 23.12.2021
Beginn: 02.01.2022
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: ja ER: unbekannt Erholt: nein

Angiogram pulmonary Cerebrovascular accident Laboratory test Ultrasound Doppler Venogram

Symptomtext

Acute CVA.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Cerebrovascular accident
Hospital-Tage: 3,0
Labordaten: CT venogram Brain, CT Angiogram Chest, US venous ext. upper bil., US venous ext. low bil., multiple labs
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfasalazine- Nausea and Vomiting, Ciprofloxacin-Headache
Vorherige Impfungen: -

VAERS 2641103

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: -
Alter: 20,0
Geschlecht: F
Eingang: 05.06.2023
Impfdatum: 11.01.2022
Beginn: 13.03.2022
Tage bis Beginn: 61,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Embolic stroke

Symptomtext

ACUTE STROKE DUE TO EMBOLISM OF UNSPECIFIED ARTERY

Weitere VAERSDATA-Felder

Praegender Schweregrund: Embolic stroke
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2636754

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: -
Alter: 41,0
Geschlecht: F
Eingang: 25.05.2023
Impfdatum: 04.02.2022
Beginn: 18.03.2022
Tage bis Beginn: 42,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Partial seizures

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE COMPLEX PARTIAL EPILEPSY, RECURRENT

Weitere VAERSDATA-Felder

Praegender Schweregrund: Partial seizures
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2623934

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: -
Alter: 45,0
Geschlecht: M
Eingang: 01.05.2023
Impfdatum: 07.01.2022
Beginn: 12.03.2022
Tage bis Beginn: 64,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Ischaemia Ischaemic stroke

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ACUTE STROKE DUE TO ISCHEMIA, UNSPECIFIED TYPE AND ARTERY

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2609169

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: MA
Alter: 21,0
Geschlecht: M
Eingang: 04.04.2023
Impfdatum: 06.01.2022
Beginn: 15.02.2022
Tage bis Beginn: 40,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Arteriogram coronary abnormal C-reactive protein increased Cardiac imaging procedure abnormal Catheterisation cardiac abnormal Chest pain Echocardiogram abnormal Electrocardiogram abnormal Electrocardiogram ambulatory Laboratory test Myocardial oedema Myopericarditis Pericardial effusion Pyrexia

Symptomtext

Patient was admitted to Hospital 2/15/22 with chest pain, fever, EKG changes and elevated C reactive protein. A coronary angiography showed normal coronary arteries with mild pericardial effusion. Suspicion was acute myopericarditis confirmed by MRI that showed edema with subepicardial non ischemic pattern in wall of left ventricle. Patient was discharged approximately 2/26/22 and allowed to fly home 3/8/22 with follow up at home. He is now doing well with no cardiac issues

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myopericarditis
Hospital-Tage: 11,0
Labordaten: Cardia Catheterization 2/15/22 MRI 2/24/22 Multiple cardia echo's Multiple EKG's labs every few days Cardia Echo 4/2022 Holter monitor 3/2022 MRI 5/25/22 Weekly labs
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: none
Allergien: PCN
Vorherige Impfungen: -

VAERS 2511858

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: MI
Alter: 78,0
Geschlecht: F
Eingang: 18.11.2022
Impfdatum: 21.12.2021
Beginn: 25.10.2022
Tage bis Beginn: 308,0
Dosis: 2
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

COVID-19 Fall Loss of consciousness SARS-CoV-2 test positive Syncope

Symptomtext

Pt to ED 10/21 with cc of fall/syncope with LOC. 10/24 Pt is aox3, on RA not in distress, denies pain or discomfort. 10/25 pt COVID+. 10/26 Pt is aox3, on RA not in distress, denies pain or sob. 10/16 pt discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 5,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Gastroesophageal reflux disease without esophagitis Gastroesophageal reflux disease without esophagitis Current use of long term anticoagulation Carotid artery stenosis Essential hypertension Mixed hyperlipidemia Chronic pain Osteoarthritis Obesity (BMI 30-39.9) Paroxysmal atrial fibrillation (CMS/HCC) Hyperglycemia Mild cognitive impairment with memory loss Lumbar foraminal stenosis CKD (chronic kidney disease), stage II Lumbar burst fracture, sequela Syncope, unspecified syncope type Permanent atrial fibrillation (CMS/HCC) Dizzinesses Fall with injury Gross hematuria LOC (loss of consciousness) (CMS/HCC) Impaired ambulation Impaired functional mobility, balance, gait, and endurance
Andere Medikamente: apixaban (ELIQUIS) 5 MG PO Tab dilTIAZem CR apixaban (ELIQUIS) 5 MG PO Tab dilTIAZem CR (CARDIZEM CD) 240 MG PO CAPSULE SR 24 HR donepezil (ARICEPT) 10 MG PO Tab HYDROcodone-acetaminophen (NORCO) 5-325 MG PO Tab nystatin (MYCOSTATIN) 100000
Allergien: None
Vorherige Impfungen: -

VAERS 2501861

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: NY
Alter: 80,0
Geschlecht: F
Eingang: 08.11.2022
Impfdatum: 30.12.2021
Beginn: 30.05.2022
Tage bis Beginn: 151,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Asthenia COVID-19 Chest X-ray abnormal Computerised tomogram head abnormal Confusional state Dysarthria Haemorrhage intracranial Lung infiltration Magnetic resonance imaging head normal NIH stroke scale score decreased SARS-CoV-2 test positive Thrombectomy

Symptomtext

5/30/2022- Presents to Ed, weakness, confusion, slurred speech. Ct head- on acute intracranial hemorrhage. Covid + test. Incidental finding. CXR- mp focal infiltrates. Ordered Bebtelovimab. Not a candidate for tPA due to low NIH score and thrombectomy d/t lack of arterial target. Ordered ASA, plavix. Pt refused anticoagulation s/t past GI bleding with Xarelto. 6/1/2022- Maintaining 02 sat. VSS 6/2/022- MRI brain negative. Stable on RA. D/C to home with stroke team and cardio f/u.

Weitere VAERSDATA-Felder

Praegender Schweregrund: NIH stroke scale score decreased
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Type 2 Dm, HTN, GERD, AFIB, TIA, CHF, and H/O R hemicolectomy
Andere Medikamente: -
Allergien: Ace inhibitors
Vorherige Impfungen: -

VAERS 2284735

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: MI
Alter: 82,0
Geschlecht: M
Eingang: 19.05.2022
Impfdatum: 23.12.2021
Beginn: 18.05.2022
Tage bis Beginn: 146,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Hypoxia Influenza virus test positive Respiratory distress Respiratory syncytial virus test positive SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough COVID infection. Mild respiratory distress, hypoxia

Weitere VAERSDATA-Felder

Praegender Schweregrund: Respiratory distress
Hospital-Tage: -
Labordaten: Positive Covid-19, Flu, RSV on 5/18/22
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroid, Alzheimer disease, dementia, hypertension
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2282931

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: AR
Alter: 36,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 15.02.2022
Beginn: 15.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Heavy menstrual bleeding Thrombosis

Symptomtext

I experienced heavy periods and blood clots

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Losartan 50MG, Phentermine
Allergien: -
Vorherige Impfungen: -

VAERS 2161625

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 05.03.2022
Beginn: 05.03.2022
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 Dyspnoea Immediate post-injection reaction Lacrimation increased Petechiae Pruritus

Symptomtext

anaphylaxis--eyes water, short of breath, itching all over, petechiae immediately. Treated with pepcid, hydroxyzine, albuterol inhaler, epipen

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: frequent anaphylaxis, unhealed wound
Vorgeschichte: hypogamaglobulinemia, selective IGE deficiency, hypermobile Ehlers-Danlos Syndrome, mast cell activation syndrome, asthma, allergies, vocal chord dysfunction, irritable bowel syndrome
Andere Medikamente: cetirizine, hydroxyzine, famotodine, nortriptyline, montelukast, budesonide, pseudoephedrine, prednisone, qvar, qnasl, epipen, albuterol, Vitamins C, D, B12, Calcium, Magnesium, Zinc
Allergien: dilaudid, buprenorphine, nucynta, tramadol (all classes of narcotics) NSAIDS, Tylenol, Penicillin, Bacitracin, Gentamicin, Metronidazole Keflex, Levaquin, Bactrim/Septra, Clindamycin, Linezolid, Vancomycin, Macrobid (nitrofurantoin), Mupirocin clotrimazole, fluconazole, terbinafine, nystatin, Cymbalta, Wellbutrin, Remeron, Lyrica, Lidoderm patch (not allergic to lidocaine or any other caine), Frova, Contrast Med (Omnipaque 300) Iohexol, Orphenadrine, Hepatitis A/B vaccine (Twinrix), DTAP (acellular pertussis, diptheria, tetanus), Flublock vaccine (2018), Tuberculin PPD, Xolair, Ketotifen, Lupron, Gastrocrom, Azelastine, Imatinib Cannot Tolerate Due to Dairy Allergy Flovent, Advair, Spiriva Cannot Tolerate Due to Polysorbate 80 Primatene Mist coconut tomato peanut sunflower seed food containing sunflower lecithin almond all other nuts or asthma dairy shrimp pineapple strawberry peach raspberry and similar berries corn basil egg anaphylaxis to airborne exposure carrot High amine foods Fermented foods Coffee dates soy sauce apple cherries Italian plums Corn Pumpernickel and Rye Pumpkin Potato Sweet potato Mango (fresh) Chocolate ice pop eggplant Cacao drink (pods) Rice Plantains, banana Root beer hard candy Wheat Oats Pork Blueberries Stamp pad ink containing castor oil perfume/cologne shampoos containing coconut lipsticks deodorant containing castor oil witch hazel Sheepskin boots Lanolin
Vorherige Impfungen: Flublock, DTAP, Twinrix

VAERS 2161625

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: NY
Alter: 56,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 05.03.2022
Beginn: 05.03.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Anaphylactic reaction Dyspnoea Immediate post-injection reaction Lacrimation increased Petechiae Pruritus

Symptomtext

anaphylaxis--eyes water, short of breath, itching all over, petechiae immediately. Treated with pepcid, hydroxyzine, albuterol inhaler, epipen

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: frequent anaphylaxis, unhealed wound
Vorgeschichte: hypogamaglobulinemia, selective IGE deficiency, hypermobile Ehlers-Danlos Syndrome, mast cell activation syndrome, asthma, allergies, vocal chord dysfunction, irritable bowel syndrome
Andere Medikamente: cetirizine, hydroxyzine, famotodine, nortriptyline, montelukast, budesonide, pseudoephedrine, prednisone, qvar, qnasl, epipen, albuterol, Vitamins C, D, B12, Calcium, Magnesium, Zinc
Allergien: dilaudid, buprenorphine, nucynta, tramadol (all classes of narcotics) NSAIDS, Tylenol, Penicillin, Bacitracin, Gentamicin, Metronidazole Keflex, Levaquin, Bactrim/Septra, Clindamycin, Linezolid, Vancomycin, Macrobid (nitrofurantoin), Mupirocin clotrimazole, fluconazole, terbinafine, nystatin, Cymbalta, Wellbutrin, Remeron, Lyrica, Lidoderm patch (not allergic to lidocaine or any other caine), Frova, Contrast Med (Omnipaque 300) Iohexol, Orphenadrine, Hepatitis A/B vaccine (Twinrix), DTAP (acellular pertussis, diptheria, tetanus), Flublock vaccine (2018), Tuberculin PPD, Xolair, Ketotifen, Lupron, Gastrocrom, Azelastine, Imatinib Cannot Tolerate Due to Dairy Allergy Flovent, Advair, Spiriva Cannot Tolerate Due to Polysorbate 80 Primatene Mist coconut tomato peanut sunflower seed food containing sunflower lecithin almond all other nuts or asthma dairy shrimp pineapple strawberry peach raspberry and similar berries corn basil egg anaphylaxis to airborne exposure carrot High amine foods Fermented foods Coffee dates soy sauce apple cherries Italian plums Corn Pumpernickel and Rye Pumpkin Potato Sweet potato Mango (fresh) Chocolate ice pop eggplant Cacao drink (pods) Rice Plantains, banana Root beer hard candy Wheat Oats Pork Blueberries Stamp pad ink containing castor oil perfume/cologne shampoos containing coconut lipsticks deodorant containing castor oil witch hazel Sheepskin boots Lanolin
Vorherige Impfungen: Flublock, DTAP, Twinrix

VAERS 2136989

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: TX
Alter: 24,0
Geschlecht: M
Eingang: 24.02.2022
Impfdatum: 21.12.2021
Beginn: 20.01.2022
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Blood creatinine normal Blood sodium normal Cerebral mass effect Computerised tomogram head abnormal Endotracheal intubation Facial paralysis Haemoglobin decreased Haemorrhage intracranial Headache Hemiparesis Immune thrombocytopenia Intensive care Platelet count decreased Sinus pain Tracheostomy Vomiting

Symptomtext

Moderna COVID Vaccine EUA: COVID-19 case resulting in Life Threatening Illness. Received Moderna Vaccine on 12/21/2021. Admitted from outside facility to ICU for acute intracranial hemorrhage and suspected immune thrombocytopenia. Presented to outside facility ED c/o HA and sinus pain, acutely developed facial droop and left sided weakness. Stat CT with evidence of intracranial hemorrhage with midline shift. Began vomiting, intubated for airway protection. Initial lab work was significant for platelet count of 1, Hgb 11, Na 140, creatinine 0.8. Received the following interventions: hypertonic saline, mannitol, steroids, and nicardipine drip. Transferred for higher level of care. Trach placed 1/31/22. Continued to improve neurologically. Sodium goals were relaxed to normonatremia and neuro checkls relaxed to q4 with q12 sodium checks and transferred to the floor on 02/20/22 with d/c plan to rehab facility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Facial paralysis
Hospital-Tage: 34,0
Labordaten: Initial lab work was significant for platelet count of 1, Hgb 11, Na 140, creatinine 0.8
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2112751

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: NJ
Alter: 77,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 21.01.2022
Beginn: 14.02.2022
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Blood lactic acid decreased COVID-19 Chest X-ray abnormal Constipation Cough Decreased appetite Influenza A virus test negative Influenza B virus test Lung infiltration Nausea Pulmonary oedema SARS-CoV-2 test positive Troponin normal White blood cell count decreased

Symptomtext

77-year-old female with past medical history of rheumatoid arthritis, scoliosis, who presented to the emergency room for evaluation of loss of appetite, cough, generalized weakness for few weeks, since getting her covid 19 booster. Patient's family states that patient has been nauseous on and off for weeks and has been constipated, and patient was supposed to see her PMD today but she came to the emergency room instead for further evaluation. In the ED, Troponin negative, influenza a and B negative, COVID-19 is positive. Lactic acid 1.03. WBC 2.6. Chest x-ray shows interstitial infiltrates versus interstitial edema.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: 2,0
Labordaten: 02/14/2022 - SARS-CoV-2 Antigen (++)
Aktuelle Erkrankungen: -
Vorgeschichte: rheumatoid arthritis, depression, scoliosis. Significant Surg Hx None. Smoking Status Former Smoker
Andere Medikamente: buPROPion HCl 150 mg Tablet Extended Release 24 hr Directions: 1 tablet oral daily (Active) foLIC Acid 0.8 mg Tablet Directions: 1 tablet oral daily (Active) tofacitinib (Xeljanz XR) 11 mg Tablet Extended Release 24 hr Directions: 1 t
Allergien: Aspirin
Vorherige Impfungen: -

VAERS 2082514

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

schwer

Staat: CA
Alter: 63,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 15.01.2022
Beginn: 02.02.2022
Tage bis Beginn: 18,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood disorder Thrombosis

Symptomtext

Systemic: Blood Disorder (diagnosed by MD)-Severe, Additional Details: wife of patient states 2 weeks after covid vaccine pt had blood clots all over his body and was hospitalized.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2068865

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: MD
Alter: 33,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest discomfort Dizziness Dyspnoea Flushing Loss of consciousness Muscle spasms Nausea Pallor Palpitations

Symptomtext

on that day 1+hour later had flushing and dizziness. had increased chest discomfort (has upcoming appointment in a few days 02/01/2022 with cardiologist for this) over sternum. had increased SOB. felt flushes. so then "passed out." husband noted that she was pale. palpitations. had nausea but no vomiting - resolved. no current lightheadedness. had increased "esophagus spasms" (working with GI for this; s/p recent EGD) no tongue/lip swelling. no rash. no fever/chills. no runny nose no hx of seizure and no seizure like activity. no loss of urine / stool continence. took Aspirin 325 mg qday - with improvement

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: No
Vorgeschichte: Erythromelalgia, Joint Pains, Dysphagia, GERD, Chest Discomfort
Andere Medikamente: Carafate 100 mg/mL susp, unsure dosing qd-TID PRN ondansetron 4 mg RD tabs, DISSOLVE 1 TABLET BY MOUTH ONCE AS NEEDED FOR NAUSEA AND/OR VOMITING pantoprazole 40 mg DR tabs, 1 tab PO qhs pregabalin 75 mg caps, TAKE 2 CAPSULES BY MOUTH TWICE
Allergien: Paxil - hallucinate
Vorherige Impfungen: flu vaccine - similar symptoms but no chest pain - last ~2017

VAERS 2068737

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: GA
Alter: 54,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 07.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Chest X-ray Computerised tomogram Disorientation Dizziness Echocardiogram Electrocardiogram Laboratory test Loss of consciousness Magnetic resonance imaging Ultrasound Doppler

Symptomtext

Dizziness, disoriented, passed out started 1/17/2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 3,0
Labordaten: Hospitalization 1/19-1/22/2022 CT scans, MRI, Lab work, EKG, Carotid ultrasound, Chest X-ray, Heart ultrasound
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety
Andere Medikamente: Trazadone, Amlodipine
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2059500

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

schwer

Staat: MI
Alter: 21,0
Geschlecht: M
Eingang: 24.01.2022
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest X-ray Chest pain Electrocardiogram Full blood count Influenza A virus test Influenza B virus test Metabolic function test Pericarditis SARS-CoV-2 test

Symptomtext

Patient started having chest pain the day after getting his 3rd Pfizer vaccine. He noted that the pain felt different than just feeling anxious and the pain persisted. Chest pains come and go over the past month and are not linked to any specific activity. A week after receiving the vaccine we went to the ER to get the pains checked out. He was put on ibuprofen 3 times a day and a diagnosis of pericarditis was given. We were referred to a cardiologist which the patient saw today. (1/24/22)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: 12/27/21: basic metabolic panel, complete blood count, High-sensitivity troponin, POCT sars-cov-2 & flu A &B, 12 lead EKG, chest x-ray. 01/24/2022: labs and EKG (scheduled for an echocardiogram on 1/31/22)
Aktuelle Erkrankungen: none
Vorgeschichte: anxiety
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2047762

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: PA
Alter: 25,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 18.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Dizziness Fall Fatigue Headache Loss of consciousness Nausea Pain

Symptomtext

Woke up feeling nauseous. Got up to walk to the restroom and became dizzy, passed-out and fell on my way to restroom. Remained on floor until dizziness subsided (maybe fell asleep for a little bit, unsure). When I got up I was no longer nauseous, so I went back to bed. I was also experienced a headache, fatigue (since injection), chills and body aches (started at approximately 10 pm). I experienced these symptoms for the first two shots, so wasn't concerned. I did not check blood pressure or temperature, I was really tired and only thought of that after I woke up this morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Gum infection treated with amoxicillin.
Vorgeschichte: Allergies, asthma, hyperhydrosis
Andere Medikamente: Zyrtec, Seasonale, Glycopyrrolate, Singulair
Allergien: N/A
Vorherige Impfungen: Headache, fatigue, body aches and chills after first 2 doses of Moderna.

VAERS 2046241

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

schwer

Staat: NC
Alter: 57,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 05.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Asthenia Chills Dizziness Feeling abnormal Influenza like illness Injection site pain Joint injury Pain Paraesthesia Syncope Tremor Unresponsive to stimuli

Symptomtext

Site: Pain at Injection Site-Severe, Systemic: Body Aches Generalized-Severe, Systemic: Chills-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Joint Pain-Severe, Systemic: Shakiness-Severe, Systemic: Tingling (specify: facial area, extemities)-Severe, Systemic: Weakness-Severe, Additional Details: patient had mild flu like symptoms after 2nd dose that lasted for about 12 hours and started 20-24 hours post vaccine. after the booster, patient's symptoms started about 20 hours later and are still continuing. patient described pain as "shooting pain thru out entire body". patient fainted twice which caused an injury to her ankle. patient is still feeling "off"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2045446

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anaphylactic reaction Condition aggravated Dyspnoea Eye swelling Mouth swelling Swelling face Swollen tongue

Symptomtext

Systemic: Allergic: Anaphylaxis-Medium, Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Medium, Additional Details: Patient stated after vaccination and allergic reaction onset that she was previously recovering from allergic/anaphylaxis reaction. She has a history of idiopathic anaphylaxis with angioedema. Patient predosed before appointment with benadryl 25 mg and self administered Amneal epinephrine as EMT arriving at pharmacy. Patient complained of swollen lips and tongue with moderate difficulty breathing. Patient brought to Hospital for follow up. Current epinephrine pen being refilled

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2044632

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21a

schwer

Staat: NY
Alter: 30,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 10.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2043763

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: FL
Alter: 24,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 15.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Injection site erythema Injection site swelling Pain Seizure Tension

Symptomtext

At approx. 2:30am I woke up to my entire body from the neck down tensing up, causing convulsions. I was fully cognizant of the event, I was able to move my body on my own. However, if I tried to remain still, various body parts would tense uncontrollably before releasing. This lasted for around 5 minutes and was becoming painful. I initially thought I was having a seizure. I have also noticed I've had a headache everyday since getting the booster which I rarely got prior. The injection cite is still red and swollen as of 01/18/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: -
Vorgeschichte: IBS, Gastroparisis
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2043155

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: MD
Alter: 22,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Condition aggravated Psychogenic seizure

Symptomtext

Patient received vaccine approximatly 10 minutes later she started to experience multiple Pseudo Seizures. POC reported patient has a history of Pseudo seizures. Patients vital signs were taken B/P-133/94 HR-113 RR-24 Spo2-99% Ems was called patient was transported to hospital at 11:15am

Weitere VAERSDATA-Felder

Praegender Schweregrund: Psychogenic seizure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Celexa
Vorherige Impfungen: -

VAERS 2034996

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: MI
Alter: 56,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Back pain Cold sweat Head injury Nausea Pain Spinal column injury Syncope

Symptomtext

Body aches, cold sweats, queasiness, Fainted, put a hole in the wall with my head and hurt my tailbone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: Urgent Care 01/09/22 for back pain, took X-rays, gave me 2 injections, one for pain and a steroid. Follow up visit with my doctor 01/14/2022
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, Lichen Sclerosis, Psoriatic Arthritis
Andere Medikamente: Claritin, Amitriptyline, Methotrexate, Folic Acid, Pilocarpine, Metoprolol supinate er, Valsartan
Allergien: Sulfa
Vorherige Impfungen: Body aches, chills following 2nd dose of Moderna 05/04/21

VAERS 2001964

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: OH
Alter: 69,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 02.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Anal incontinence Disorientation Dizziness Fatigue Feeling abnormal Gait disturbance Movement disorder Pain in extremity Syncope

Symptomtext

At about 5am the morning after, got up and got dizzy enough to faint. For about 15 min.. lost complete body functions. Could not move my own body and had uncontrollable bowel movement. After getting help back to bed, was very disoriented for awhile until able to sleep. Still very tired today with sore arm but getting back to normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Losartan 50mg
Allergien: None
Vorherige Impfungen: -

VAERS 1989116

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: RI
Alter: 25,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Flushing Hyperhidrosis Loss of consciousness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Mild, Additional Details: Patient received Moderna booster. RN gave the vaccine and reported the patient fainted and was unconcious for around 2 seconds. Rescue was called. Patient was cleared to go home

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1980915

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: NJ
Alter: 25,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 24.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

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: -

VAERS 1978968

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: PA
Alter: 23,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Immediate post-injection reaction Syncope Unresponsive to stimuli Vomiting

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Systemic: Vomiting-Mild, Additional Details: Patient stated that she has a history of fainting after vaccines. Immediately after she felt lightheaded and then a couple mintes after she fainted for a few seconds. A couple minutes later she vomitted. She stayed seated for several minutes until feeling better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1974492

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: MO
Alter: 28,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Anaphylactic reaction Eye swelling Flushing Headache Hyperhidrosis Hypoaesthesia Mouth swelling Paraesthesia Swelling face Swollen tongue

Symptomtext

Systemic: Allergic: Anaphylaxis-Mild, Systemic: Allergic: Swelling of Face / Eyes / Mouth / Tongue-Mild, Systemic: Flushed / Sweating-Mild, Systemic: Headache-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild

Weitere VAERSDATA-Felder

Praegender Schweregrund: Anaphylactic reaction
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1974462

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

schwer

Staat: CT
Alter: 37,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Medium

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1968620

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

schwer

Staat: NY
Alter: 18,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Electrocardiogram Syncope

Symptomtext

Patient fainted shortly after administration of vaccine. She was AAO, breathing normally, and responsive. 911 was called at time of event, ambulance was dispatched to scene for medical follow up of patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: EKG
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1962290

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

schwer

Staat: VA
Alter: 33,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 19.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Face injury Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Additional Details: Roughly 1 minute s/p injection(1200). Bystander states patient should talk to pharmacist about that. Bystander states patient fainted out of seat and hit face on floor and was awoken on impact. vitals 100/86 bp 66 pulse. pt then stated that she had history of syncope with injections upon further dialogue. emts called onto scene. patient declined transport and care. pt stated "feelings" are gone and left scene at 1241.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2670181

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: -
Alter: 60,0
Geschlecht: F
Eingang: 11.08.2023
Impfdatum: 21.12.2021
Beginn: 23.02.2023
Tage bis Beginn: 429,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Hypotension

Symptomtext

HYPOTENSION

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2670077

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: -
Alter: 75,0
Geschlecht: F
Eingang: 11.08.2023
Impfdatum: 29.12.2021
Beginn: 12.03.2023
Tage bis Beginn: 438,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Hypotension

Symptomtext

HYPOTENSION

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2618316

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: -
Alter: 63,0
Geschlecht: F
Eingang: 20.04.2023
Impfdatum: 10.02.2022
Beginn: 19.08.2022
Tage bis Beginn: 190,0
Dosis: 2
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Hypotension Symptom recurrence

Symptomtext

HYPOTENSION 11/17/2022 - RECURRENCE OF SAME SYMPTOMS

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2608326

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: CT
Alter: 61,0
Geschlecht: M
Eingang: 03.04.2023
Impfdatum: 02.04.2022
Beginn: 07.11.2022
Tage bis Beginn: 219,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Cough Dyspnoea Fatigue Headache Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

11/8 around 2 AM woke up with headache and cough felt run down and congested. Took COVID-19 test and it was positive. Drank lots of fluids. By 11/10 was feeling short of breath and was told to go to ER. Had violent and painful cough. Had headache and shortness of breath. My resting HR was 120 and pulse OX was 98%. Was released with prescription for cough syrup and cough pills. PCP called to follow up and prescribed PAXLOVID and ADVAIR. Symptoms began improving but wasn't fully recovered for about 3 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Tinnitus, acid reflux; Meniere's disease
Andere Medikamente: Pantoprazole; LIPO-FLAVONOID; vitamin D plus calcium; ALLEGRA
Allergien: White birch allergy
Vorherige Impfungen: -

VAERS 2608105

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MI
Alter: 63,0
Geschlecht: M
Eingang: 03.04.2023
Impfdatum: 25.03.2022
Beginn: 27.03.2023
Tage bis Beginn: 367,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Abdominal pain Asthenia COVID-19 Chest pain Decreased appetite Diarrhoea Dyspnoea Nausea Productive cough SARS-CoV-2 test positive Vomiting

Symptomtext

Discharge summary "This is a 64 YO male with history of HTN, T2DM, CKD St3, hyperlipidemia, CAD, depression, PVD, Bil BKA, who presented with generalized weakness and diarrhea for several months. Patient seen and examined and was noted to be awake, alert, and oriented x 4, conversant, in no acute distress. Patient reports feeling weak for the last few months with associated watery diarrhea, loss of appetite, generalized abdominal pain, nausea and vomiting. Describes pain as punch-like pain, all over his abdomen with no pain radiation. Denies recent international travels. Patient could not quantify the number of watery stools in one day. Kept saying " a lot" .Patient states that he had chest pain and shortness of breath which resolved but still with productive cough for the last few weeks. Denies sick contacts. Denies fever, chills, headache, dizziness, rectal pain, rectal bleeding, dysuria. Reports he was just released from the the hospital 2 weeks ago and also had diarrhea before and after hospitalization. Patient given because COVID positive on 03/27 without any respiratory symptoms. He was ready for discharge but his facility did not have isolation next so he was kept overnight and discharged on 03/31 in stable condition. "

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 4,0
Labordaten: COVID positive PCR test on 3/27/2023
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2570601

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) · Charge 068H21A

moderat

Staat: GA
Alter: 23,0
Geschlecht: M
Eingang: 30.01.2023
Impfdatum: 05.12.2022
Beginn: 15.12.2022
Tage bis Beginn: 10,0
Dosis: 1
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Aortic dilatation Chest pain Echocardiogram abnormal Mitral valve incompetence Palpitations

Symptomtext

Pt developed chest pain and heart palpitations 10 days after vaccination. Upon workup with cardiologist, pt was found to have mitral regurgitation, dilated aortic root, and dilated ascending aorta. Pt had no symptoms prior to vaccination. Pt was previously a healthy, active 23 year old.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 1/13/23: cardiac echocardiogram showing EF- 55-60%, dilated aortic root, dilated ascending aorta
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2568790

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: ME
Alter: 53,0
Geschlecht: M
Eingang: 26.01.2023
Impfdatum: 25.01.2022
Beginn: 22.12.2022
Tage bis Beginn: 331,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Chest X-ray normal Chills Cough Dyspnoea Fatigue Hypersomnia Influenza Influenza A virus test positive Mobility decreased Pain Pyrexia SARS-CoV-2 test negative Wheezing

Symptomtext

In mid-December 2022 I began to wheeze and cough. It became more difficult to breath on December 22, 2022. I had a low-grade fever. I visited an urgent care on this day and tested positive for Influenza A. I am still recovering and having trouble breathing. My cough was a dry, deep, barking. I then had body aches and slept for 36 hours straight I was so exhausted I could not move. I was so fatigued I had to crawl to the restroom. I was prescribed Tamiflu. My fever lasted for about 3 days and was accompanied with chills. My lingering symptoms are coughing and difficulty breathing as well as fatigue. I nap all the time and just cannot seem to stay awake. In early January, I went to the emergency department at 3:00am because I could not breathe. They gave me a nebulizer treatment and it did not help. They did a chest X-Ray and it was negative for pneumonia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Influenza, positive, 12222022; Pneumonia, negative, 12222022; COVID-19, negative, 12222022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Crohn's Disease
Andere Medikamente: Gabapentin; Vyvanse; Wellbutrin; Pantoprazole; Vitamin D3; Trintellix; Metoprolol; Finasteride
Allergien: Penicillin; Tree nuts; Vegetables and Fruits; Gluten; Seasonal environment
Vorherige Impfungen: -

VAERS 2566833

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MI
Alter: 89,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 23.12.2021
Beginn: 26.12.2022
Tage bis Beginn: 368,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Dyspnoea

Symptomtext

12/26/22 presents to ED for "breathing problem". PMHx of "afib, DM, HLD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2557470

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: SC
Alter: 38,0
Geschlecht: F
Eingang: 11.01.2023
Impfdatum: 08.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Condition aggravated Headache Hypersensitivity Injection site pain Pain

Symptomtext

I had extreme chills, body aches and pain at injection for about a week. My allergies got worse after the vaccine, and I developed headaches. I would take something for my headache and sometimes it would work and sometimes not. I would increase hydration and that would help. I did see my doctor and they started me on medicine that is helping. As of today, the headaches have not gotten better but they haven't got worse. I am dealing with them on a daily basis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism; Diverticulitis
Andere Medikamente: Ibuprofen; iron; vitamin D; multivitamin; turmeric; lysin; B complex; ashwagandha root; vitamin C; glucosamine; ALLEGRA; caffeine; SUDAFED; SYNTHROID
Allergien: Hay Fever
Vorherige Impfungen: -

VAERS 2545763

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 31,0
Geschlecht: M
Eingang: 29.12.2022
Impfdatum: 27.12.2021
Beginn: 18.12.2022
Tage bis Beginn: 356,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Cough Dyspnoea Influenza virus test Malaise Nasopharyngitis Rhinorrhoea SARS-CoV-2 test

Symptomtext

I was having a runny nose and a slight cough and thought I had sinus infection, so I went back to doctor because I had a cold previously. They tested me for Influenza and COVID-19 and that was on Tuesday the 20th. I was not having to hard of a time but right before Christmas I was really sick. I was having a cough, shortness of breath, and while I was having chills, I did not have a fever. When I had gone in for my cold, they had tested for COVID-19 and it was negative when I had gone into the doctor two weeks prior for my cold.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 PCR test; Influenza; COVID-19 home test
Aktuelle Erkrankungen: N/A
Vorgeschichte: High Blood Pressure
Andere Medikamente: Omeprazole; amlodipine
Allergien: N/A
Vorherige Impfungen: -

VAERS 2496780

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: VA
Alter: 51,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 30.01.2022
Beginn: 30.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Asthma Cardiac monitoring Dyspnoea Electrocardiogram Heart rate decreased Heart rate increased Ultrasound scan

Symptomtext

Trouble breathing, heart rate really high then would drop really low, had a full blown asthma attack, had to go get nebulizer treatment, inhaler and steroids. Was put on heart monitor, had heart sonogram, EKG. Heart rate is still messed up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Nebulizer treatment Inhaler Steroids EKG Sonogram Heart monitor to wear 24/7
Aktuelle Erkrankungen: No
Vorgeschichte: From the vaccine =yes
Andere Medikamente: None
Allergien: Severe allergies, took allergies shots many years
Vorherige Impfungen: -

VAERS 2496427

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MI
Alter: 88,0
Geschlecht: F
Eingang: 02.11.2022
Impfdatum: 19.01.2021
Beginn: 06.09.2022
Tage bis Beginn: 595,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Atrial fibrillation COVID-19 Condition aggravated SARS-CoV-2 test positive

Symptomtext

09/06/22 presents to ED for "A. fib". PMHx of "A. fib."

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 09/06/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2475246

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

moderat

Staat: RI
Alter: 61,0
Geschlecht: F
Eingang: 11.10.2022
Impfdatum: 07.03.2022
Beginn: 01.04.2022
Tage bis Beginn: 25,0
Dosis: N/A
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: unbekannt

Arrhythmia Arthropathy Blood thyroid stimulating hormone normal Borrelia test negative C-reactive protein increased Cognitive disorder Condition aggravated Echocardiogram normal Electrocardiogram abnormal Electrocardiogram ambulatory abnormal Extrasystoles Fatigue Hypersomnia Impaired work ability Magnetic resonance imaging head Magnetic resonance imaging heart Neuropathy peripheral Red blood cell sedimentation rate increased

Symptomtext

I am a physician with a decade long hx of post-viral autoimmune disorder, working halftime due to this. This typically flares with infections. I Had J&J shots x 2 , no problem. Did ok with Moderna shot for a couple weeks, then joints, fatigue and neuropathy flared badly, followed by overwhelming fatigue, persistent bigeminy and trigeminy, cognitive problems. I had to stop clinical work with patients due to concerns about cognition, and have dropped down to 3-5 hours work weekly. My immunologist thinks I had a big IgG surge a few weeks after the vaccine, which set off the problem. My neurologists think I have post-vaccination hypersomnia due to specific effects of inflammatory mediators on specific parts of the brain. They say I may or may not get better. My cardiologists think the physiologic stress of the inflammatory surge caused cortisol and adrenaline surge which kicked off arrhythmia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Echocardiogram normal spring 2022. Holter and EKG showing LBBB, frequent ectopy including bigeminy and trigeminy. Labs showed elevated ESR and CRP. covid nucleocapsid antibody and lyme tests and TSH negative. Brain MRI, polysomnogram, and cardiac MRI are pending.
Aktuelle Erkrankungen: none acute
Vorgeschichte: autoimmune arthropathy and neuropathy, familial vibratory urticaria, exercise induced Left bundle branch block, obesity, hyperlipidemia
Andere Medikamente: methotrexate, crestor, zetia, atenolol, folate
Allergien: enbrel, humira
Vorherige Impfungen: -

VAERS 2467278

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MI
Alter: 73,0
Geschlecht: F
Eingang: 03.10.2022
Impfdatum: 22.01.2022
Beginn: 20.09.2022
Tage bis Beginn: 241,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute kidney injury Asthenia Blood creatinine increased Blood electrolytes Blood lactic acid decreased COVID-19 Electrocardiogram T wave inversion Electrocardiogram abnormal Fatigue Full blood count normal Hypoxia Malaise Muscular weakness Nervousness Pyrexia Respiratory rate increased SARS-CoV-2 test positive Tachycardia

Symptomtext

Date of Admission: 9/20/2022 Discharge Date: 9/22/2022 PRESENTING PROBLEM: Hypoxia [R09.02] Elevated troponin [R77.8] AKI (acute kidney injury) COVID [U07.1] COVID-19 virus infection [U07.1] HOSPITAL COURSE: Patient is a 73 y.o. female who presents today with fatigue. pmh htn,obesity,gerd, depression and anxiety, dm 2. Notes onset today with " non feeling well. Noted onset feeling shaky and legs feeling weaker than normal. In ed found to be hypoxic to 88% on room air requiring 2 l nc o2. cxr neg for acute process. Febrile to 38.1 tachycardic , rr elevated . Labs with creat 1.36 last obtained in 2017 0.69. troponin baseline 22 with 2 hr pending . Ecg with diffuse t inversion v1 v6 no st abnormality. Lactic 1.2 cbc normal ranges . Tested positive for covid . Given fluids 2 liters , decadron ,tylenol in ed . Hospitalist service consulted for admission further evaluation. She was continued on COVID-19 therapy with dexamethasone and remdesivir. She was continued on severe respiratory isolation. Supplemental oxygen was continued and weaned to room air. She is noted to have continued generalized weakness needing assistance greater than her baseline. PT/OT evaluated and advised home with assist and no additional services needed upon discharge. MSW/CM on board for discharge plan referral and arranging outpatient services. Electrolytes were monitored and repleted throughout the admission. Patient clinically improved and hemodynamically stable for discharge. Discussed plan of care discharge with patient including outpatient follow-up PCP within 7 days. Patient voiced understanding was agreeable with plan of care discharge.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tachycardia
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Pre-operative cardiovascular examination Diabetes mellitus, type II (HCC) Essential hypertension, benign Dyslipidemia Closed fracture of proximal end of right humerus, unspecified fracture morphology, initial encounter Closed displaced fracture of fourth metacarpal bone of right hand with routine healing, unspecified portion of metacarpal, subsequent encounter Depression Class 3 severe obesity in adult (HCC
Andere Medikamente: acetaminophen (TYLENOL) 500 MG tablet ALPRAZolam (XANAX) 0.25 MG tablet benzonatate (TESSALON) 100 MG capsule buPROPion (WELLBUTRIN SR) 100 MG 12 hr tablet Calcium-Phosphorus-Vitamin D (CITRACAL +D3 PO) Cholecalciferol (VITAMIN D-3 PO) ezet
Allergien: Ibuprofen Propoxyphene N-apap Soma [Carisoprodol]
Vorherige Impfungen: -

VAERS 2420926

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MI
Alter: 70,0
Geschlecht: M
Eingang: 26.08.2022
Impfdatum: 27.01.2021
Beginn: 11.08.2022
Tage bis Beginn: 561,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

COVID-19 Constipation Dyspnoea Fatigue Headache Leukopenia Productive cough Pyrexia SARS-CoV-2 test positive White blood cell count decreased

Symptomtext

Pt to ED 8/11 for dyspnea. Pt c/o moist cough, generalized fatigue, fever, and SOB. COVID+ 8/11, prior infection in July,continue decadron, rx empiric ceftriaxone and Zithromax for possible bacterial superinfection. 8/13 pt AxOx4, VSS, no c/o pain. 8/14 pt alert and oriented x 4 C/O constipation, denies pain, pt with worsening leukopenia. Pt started on granix and leucovorin calcium due to low WBC. 8/15 Pt A&Ox4, ambulatory/independent. Denies pain or SOB. 8/17 leukopenia improved, remained a+ox4 c c/o headache pain relieved with prn pain meds. 8/18 pt received/remained A+ox4 c c/o mild pain at head 3/10 throughout. 8/19 Patient is A&O x 4. Ready for discharge. Pt discharged 8/ 19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 8,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Atopic rhinitis ... Atopic rhinitis Pneumonia due to COVID-19 virus CAP (community acquired pneumonia) Hypothyroid Postoperative hypothyroidism Rheumatoid arthritis with positive rheumatoid factor (CMS/HCC) Methotrexate, long term, current use Rheumatoid arthritis (CMS/HCC) Essential hypertension Anxiety Acute onset aura migraine Multiple-type hyperlipidemia Fatigue Elevated fasting blood sugar Generalized anxiety disorder Screening for colon cancer Peyronie disease Medicare annual wellness visit, subsequent Nicotine dependence, chewing tobacco, uncomplicated Need for zoster vaccine Need for influenza vaccination Benign paroxysmal positional vertigo due to bilateral vestibular disorder Primary osteoarthritis of left knee Tear of medial meniscus of left knee, current Depression, recurrent (CMS/HCC) Pre-operative clearance Bleeding risk due to aspirin COVID-19 Neutropenia (CMS/HCC)
Andere Medikamente: albuterol (PROVENTIL, VENTOLIN, PROAIR) ... albuterol (PROVENTIL, VENTOLIN, PROAIR) HFA 108 (90 Base) MCG/ACT INHAL Aero Soln cyclobenzaprine (FLEXERIL) 10 MG PO Tab Dexamethasone 6 MG PO Tab diclofenac sodium (VOLTAREN) 1 % EXTERNAL Gel f
Allergien: None
Vorherige Impfungen: -

VAERS 2408938

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: TX
Alter: 50,0
Geschlecht: F
Eingang: 11.08.2022
Impfdatum: 04.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injected limb mobility decreased

Symptomtext

Left shoulder still does not have full mobility. Prior to second vaccination, I had no mobility issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2395006

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: GA
Alter: 64,0
Geschlecht: F
Eingang: 28.07.2022
Impfdatum: 26.01.2022
Beginn: 25.02.2022
Tage bis Beginn: 30,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Burning sensation Chapped lips Dyspnoea Lip pain Palpitations Pruritus Rash Skin exfoliation

Symptomtext

A month after receiving the vaccine my eyelids and eyebrows were very itchy and flaky. This progressed to forehead, lips, forearms down to the tops of my hand. If I would sweat my face would burn. I called my doctor who has prescribed Cortisone 10 to help with the itching. The rash will go away but it always comes back, currently the corners of my mouth are cracked and hurting. I have been experiencing shortness of breath and heart palpitations. I have an appointment to see a dermatologist in September as I have never had anything like this before.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes; High Blood Pressure
Andere Medikamente: Janumet; Losartan; Kirkland Triple Action Joint Health; Omeprazole
Allergien: No
Vorherige Impfungen: -

VAERS 2379693

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: TX
Alter: 50,0
Geschlecht: F
Eingang: 22.07.2022
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Headache Migraine

Symptomtext

I had a serve migraine, it lasted for 24 hours. That night I took Hydrocodone I had on hand, then during the day I took Tylenol and it managed the pain. I continued to have headaches for the duration of the week, lasting about 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypertension
Andere Medikamente: Lisinopril; Flonase; Multivitamin
Allergien: Demerol
Vorherige Impfungen: -

VAERS 2361157

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: -
Alter: 40,0
Geschlecht: F
Eingang: 07.07.2022
Impfdatum: 05.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Abdominal distension Anxiety Blood test Decreased appetite Disability Ear discomfort Fatigue Feeling abnormal Mechanical urticaria Mobility decreased Nervous system disorder Poor quality sleep Pruritus Rash erythematous Rash papular Skin warm Urticaria

Symptomtext

I started itching on my upper body then it moved all over from head to toe. I was getting bumps and rash on random places. Even the inside of my ears were itchy. I got red bumps and raised whelps where I touched and was hots. I contacted my doctor and was diagnosed with dermatographia. I am on Zyrtec now. The rash went away and the itching is still ongoing and I still have to take Zyrtec. I have Myalgic Encehalomyelitis and made a VAERS report on dose 2. I have more brain fog, fatigue, and could no longer function like I use to. I am now on disability. My nervous system and anxiety is worse. I was sleeping poorly and lost my appetite. I have bloating as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Blood work
Aktuelle Erkrankungen: Bronchitis
Vorgeschichte: Myalgic Encephalomyelitis; Migraines
Andere Medikamente: Motegrity; Albuterol; Steroid Inhaler
Allergien: Sulfa; Codeine; Erythromycin
Vorherige Impfungen: Moderna 2nd dose - vaers report submitted. Flu - 2019 - swelling at injection site and flu symptoms

VAERS 2357789

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 05.07.2022
Impfdatum: 01.04.2022
Beginn: 15.05.2022
Tage bis Beginn: 44,0
Dosis: 4
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Ageusia Anosmia COVID-19 Chills Cough Dyspnoea Fatigue Headache Myalgia Nasal congestion Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I contracted Covid, confirmed by testing. Symptoms: fever, cough, shortness of breath (O2 levels did not drop below 92), sore throat (extremely severe), loss of taste or smell, chills, muscle aches, headaches, fatigue (extreme), and nasal congestion. Dr. put me on Paxlovid due to my being immunocompromised according to my rheumatologist (who had just moved out of state.) I recovered from the worst of the symptoms and tested negative on day 8. By the evening of day 9 my symptoms were returning and I tested positive again. I then had a rebound case in which the sore throat was not as bad but the headaches were much worse. I finally tested negative again 22 days after my original positive test. I continue to suffer from fatigue and get winded very easily. I also get low level headaches frequently now where I used to only get one headache a month or so.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Husband had symptoms on May 14 but tested negative with an antigen tests. Symptoms continued so he got a PCR on May 15 and tested positive with PCR. I then took an antigen test which was also positive on May 15. Two more antigen tests were negative for me on May 22 and May 23. Symptoms started to return so I retested and was positive again on May 24. Finally tested negative again on June 4 and again on June 6.
Aktuelle Erkrankungen: Seasonal allergies
Vorgeschichte: Ankylosing spondylitis, variety of arthritis
Andere Medikamente: Celebrex, Plaquenil, Jumelle-FE, B-12, D-3, multivitamin, Allegra, Magnesium,
Allergien: Aspirin, erythromycin, penicillin, Imitrex, Ginger, Cumin, dusts, molds, pollens
Vorherige Impfungen: -

VAERS 2325610

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MA
Alter: 48,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 19.12.2021
Beginn: 09.06.2022
Tage bis Beginn: 172,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

COVID-19 Chest discomfort Chest pain Cough Diarrhoea Fatigue Nasal congestion Pain SARS-CoV-2 test positive

Symptomtext

It started with severe nasal congestion. I went to my doctor for nasal spray. From there, I developed a little cough. I also was experiencing some chest pressure and some chest pain. At that point, I decided to take an at home COVID-19 test which was positive. I went to the emergency room for my chest pain. I had extreme fatigue, body aches and diarrhea. This lasted for 5 days and I took Paxlovid. I still have a lingering cough.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Yes
Andere Medikamente: Medication
Allergien: Codeine
Vorherige Impfungen: -

VAERS 2311550

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 52,0
Geschlecht: M
Eingang: 07.06.2022
Impfdatum: 01.04.2021
Beginn: 21.06.2021
Tage bis Beginn: 81,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: ja Erholt: nein

Abdominal discomfort Back pain Echocardiogram Electromyogram Gait disturbance Intervertebral disc protrusion Magnetic resonance imaging neck Magnetic resonance imaging spinal abnormal Muscular weakness Neck pain Paraesthesia Quantitative sudomotor axon reflex test Spinal X-ray Ultrasound Doppler Vertigo Vibratory sense increased X-ray limb

Symptomtext

Prior to receiving the Moderna shots, I had pin and needle sensations in extremities from catching Covid 19 in January 2021. By middle of February 2021 tested negative. After receiving the 2nd moderna vaccine around 8 weeks later started having stomach issues, pin and needle feeling in extremities became stronger, weakness in legs when starting to walk. A week later started experiencing severe lower back pain and mild neck pain. By end of September 2021 I had developed vertigo and internal vibrations...

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: US, Duplex, Venous, lower extremities; US, Echocardiogram; X-ray of knee x2; Pulse Volume Recording; Sudomotor testing of Autonomic nervous system; Electromyogram; Sudomotor testing of Autonomic nervous system function (proc); X-ray Cervical; X-ray Lumbar; MRI Cervical; MRI Lumbar. MRI's did show 3 herniated disk with one protruding on spinal cord.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Gabapentin
Allergien: No
Vorherige Impfungen: -

VAERS 2309619

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: IL
Alter: 27,0
Geschlecht: M
Eingang: 04.06.2022
Impfdatum: 04.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Angina pectoris Anxiety Blood pressure increased Blood test normal Chest X-ray Chest pain Computerised tomogram thorax Dizziness Echocardiogram normal Electrocardiogram abnormal Fibrin D dimer Headache Heart rate irregular Hyperhidrosis Hypoaesthesia Migraine Mobility decreased Muscle twitching

Symptomtext

3 Months after Report (March 30th, 2022): 27M 6'0" 190(s)lbs, pretty active Shot 1-2: Pfizer, Booster: Moderna (early January) Doctor's appointment (2hrs later) after booster, my BP was 168/110. My BP in November was 124/84. 24 hours after the booster, I got real bad stabbing chest pain and dizzy headaches. Went to ER 48hrs after booster. BP : 170+/100+, HR: 100+ after getting up from sleep, sweating a lot. ECG: abnormal with possible enlarged heart CT (d-dimer elevated), X-Ray, blood tests came back fine. Discharged with "anxiety" like others here. BP was 155/105 when discharged. PCP put me on a beta-blocker. Beta blocker kept it in the high 140s and sometimes high 130s. Helped with keeping HR low. The beta-blocker gives me dizzy spells so not ideal. Had muscle twitches randomly throughout the day (entire body) for a month or so, has settled to extremely rarely now. I also had bad migraines on the right side of my head daily (5 secs - 2 min). Never had migraines ever before. My hands would also sometimes feel like falling asleep numbness. I also would get random hypnic jerks when trying to fall asleep for two months. Tried to exercise about 3 weeks after the booster(very light, 1 mile), heart beating crazy out of my chest. Hours later, heart pain was back like day 1. Subsided back to manageable levels 24 hours later. Tried lifting light weights and again light exercise (walking) a few weeks later. Was able to lift and walk but at the end of my workouts, heart pain would come back for a few hours. My baseline BP seemed to change after my booster to 150s and 160s. Doing anything (walking to my car, laundry, etc) seemed to elevate my BP and HR a lot more than it should have. Also took exceedingly long to return to "normal". Gave blood once (barely passed HR/BP conditions). It seemed to help. Tried giving Plasma but didn't meet conditions. I basically have a BP in public phobia now. Got an Echocardiogram and Kidney ultrasound from my Cardiologist. Both came back fine, no myocarditis thankfully. I was put on an ACE Inhibitor/diuretic a few weeks back and my BP is back to 120/70+ in the mornings and a bit higher later in the day. I am hoping to get off these as soon as I can. First month was debilitating and I was basically bed-ridden. Second month I could function but couldn't do anything strenuous or inflammatory. Third month, I felt almost back to normal me with help of meds. Currently I have very faint heart pain. Greatly reduced after starting the ACE Inhibitor. HR can still be somewhat high at rest. My BP is basically normal with anti-ace meds. Helpful Solutions: - Hibiscus Tea (acts like an ACE Inhibitor) - Low dose aspirin (when needed) - Small meals, healthy foods. - Giving Blood/Plasma - Sleep aids Avoid/Harmful: - Inflammatory meals and/or large meals (BP, HR, and chest pain skyrockets for hours after) - Exercise (try walking for 20 minutes and then increase gradually) - ALCOHOL (tried drinking a couple times (6 beers) and my HR would go crazy that night. I seem to be able to drink now with milder side effects)

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CT Scan (chest) - 1/6/2022 Troponin - 1/6/2022 XRay (chest) - 1/6/2022 D-Dimer - 1/6/2022 Echocardiogram - 3/1/2022 Kidney Ultrasound - 3/7/2022
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2288084

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MI
Alter: 29,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood testosterone normal Chest discomfort Chest pain Chills Dyspnoea Fatigue Electrocardiogram abnormal Exercise tolerance decreased Fear Full blood count normal Oestradiol normal Pyrexia Sinus arrhythmia

Symptomtext

On 5/20/22, my patient described the following events: They received their Moderna booster on 12/20/2021 and suffered intense side effects afterward, which were very unlike their side effects after Pfizer COVID-19 vaccines. "It was scary." Right after vaccination, they came down with fevers and chills. About 12 hours later, they felt "really intense chest pain like stabbing tightness in [their] central chest." The severe chest pain lasted 3 days and was followed by unusual exertional fatigue, such that even walking up a flight of stairs resulted in exhaustion and shortness of breath. Over the next 2 weeks, the fatigue resolved and now they are back to regular exercise and good health.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: I ordered an EKG on 5/20/22, but this was already 5 months after the incident. EKG showed normal sinus rhythm with sinus arrhythmia. CBC, testosterone and estradiol levels on 5/20/22 were within normal limits.
Aktuelle Erkrankungen: None
Vorgeschichte: Depression Testosterone deficiency
Andere Medikamente: ? buPROPion (WELLBUTRIN XL) 150 mg 24 hr tablet Take 3 tablets (450 mg) by mouth every morning. ? testosterone (ANDROGEL) 1.62 % (20.25 mg/1.25g actuation) TD gel pump Place 1 pump actuation onto the skin once daily.
Allergien: None
Vorherige Impfungen: -

VAERS 2288084

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MI
Alter: 29,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood testosterone normal Chest discomfort Chest pain Chills Dyspnoea Fatigue Electrocardiogram abnormal Exercise tolerance decreased Fear Full blood count normal Oestradiol normal Pyrexia Sinus arrhythmia

Symptomtext

On 5/20/22, my patient described the following events: They received their Moderna booster on 12/20/2021 and suffered intense side effects afterward, which were very unlike their side effects after Pfizer COVID-19 vaccines. "It was scary." Right after vaccination, they came down with fevers and chills. About 12 hours later, they felt "really intense chest pain like stabbing tightness in [their] central chest." The severe chest pain lasted 3 days and was followed by unusual exertional fatigue, such that even walking up a flight of stairs resulted in exhaustion and shortness of breath. Over the next 2 weeks, the fatigue resolved and now they are back to regular exercise and good health.

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: I ordered an EKG on 5/20/22, but this was already 5 months after the incident. EKG showed normal sinus rhythm with sinus arrhythmia. CBC, testosterone and estradiol levels on 5/20/22 were within normal limits.
Aktuelle Erkrankungen: None
Vorgeschichte: Depression Testosterone deficiency
Andere Medikamente: ? buPROPion (WELLBUTRIN XL) 150 mg 24 hr tablet Take 3 tablets (450 mg) by mouth every morning. ? testosterone (ANDROGEL) 1.62 % (20.25 mg/1.25g actuation) TD gel pump Place 1 pump actuation onto the skin once daily.
Allergien: None
Vorherige Impfungen: -

VAERS 2292673

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: VA
Alter: 74,0
Geschlecht: M
Eingang: 24.05.2022
Impfdatum: 14.04.2022
Beginn: 17.04.2022
Tage bis Beginn: 3,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Burning sensation Herpes zoster Paraesthesia SARS-CoV-2 test negative Sensitive skin Skin lesion

Symptomtext

I experienced at first a slight tingling and burning sensation on left side - mid chest and continued to my back. I consulted with Doctor and she confirmed shingles as I showed her the lesions on my side. I was prescribed an opioid which I refused. I used a topical spray with lidocaine and capsaicin patches without relief. .Gabapentin was then prescribed which I did not want to take either. I used ibuprofen and after a few weeks it has gradually get better. I still have skin sensitivity, but it is gradually disappearing. I have been testing my self with a rapid COVID test once per week. I have never had a positive test. Sx are improving.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Home testing for COVID 1 time per week.
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: no prescriptions, Vitamin D3, C, probiotic, B complex
Allergien: no allergies
Vorherige Impfungen: -

VAERS 2278986

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: FL
Alter: 43,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 17.03.2021
Beginn: 20.03.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anxiety Arthralgia Bladder disorder Depression Dyspepsia Dyspnoea Inflammation Insomnia Neck pain Sinusitis Weight decreased Weight increased

Symptomtext

Trouble breathing. Sinus Infections. Constant pain in my right shoulder. Constant pain in my neck. Bladder problems. Indigestion. Trouble sleeping. Anxiety, depression. Constant inflammation throughout my body. Weight gain/weight loss. Mostly weight gain.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Pleurisy
Vorgeschichte: Rheumatoid Arthritis Hypothyroidism
Andere Medikamente: Albuterol HFA 2 puffs as needed Quetiapine 100 MG at night Alprazolam 1MG as needed Omeprazole DR 40MG Once a day Zolpidem Tartrate 10MG at night Levothyroxine 75 MCG Valacyclovir 500MG Azelastine 0.1% Spray Daily Women's 1 a day Multi-Vit
Allergien: Environmental allergies to dust, mold, trees, some grasses, and pollen.
Vorherige Impfungen: -

VAERS 2271171

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: -
Alter: 83,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 12.02.2021
Beginn: 26.01.2022
Tage bis Beginn: 348,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Chest pain Dyspnoea Productive cough SARS-CoV-2 test positive

Symptomtext

01/26/22 presents to ED for "chest pain, SOB, and productive cough". PMHx of "CAD and MI s/p stents, HFpEF (EF 45%), chronic neck pain, CVA, DM type 2 (on Levemir), HLD, DVT s/p IVC filter (on Lovenox), HTN, CKD stage IIIb, macrocytic anemia, PAD, neuropathy, seizure, and TIA"

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 01/26/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2263430

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 18.05.2021
Beginn: 16.01.2022
Tage bis Beginn: 243,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Acute kidney injury COVID-19 Cellulitis Condition aggravated Dehydration Dizziness Glycosylated haemoglobin decreased Hypertension SARS-CoV-2 test positive Sinus disorder Staphylococcal bacteraemia

Symptomtext

Provider notes: "Patient is a 64-year-old female with a past medical history of obesity, type 2 diabetes mellitus who presented with MRSA bacteremia from left upper extremity cellulitis. Completed > 2 week course of daptomycin. Had issues with hypertension which improved mostly with adding diuretic and BB. Unfortunately, became dehydrated and had mild AKI which improved with IV fluids. Had Issues with dizziness, suspect to be secondary to sinuses (chronic problem) and improved with treatment of sinuses. Her long-acting insulin regimen has been decreased at this time, with A1 c 7.2. She has been restarted on her home meds. This regimen will need to be titrated over time. The patient has been asked to check her blood sugars 3 times a day and before bed and report these to PCP. Home care has been arranged, and the patient has been in contact with her caregivers and they plan to meet her at home today."

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 36,0
Labordaten: Positive COVID PCR 1/16/22
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension (Chronic) Unknown Type 2 diabetes mellitus with diabetic neuropathy, with long-term current use of insulin (HCC) Unknown Asthma Unknown Arthritis Unknown GERD (gastroesophageal reflux disease) Unknown Hypothyroidism Unknown Morbid obesity with BMI of 70 and over, adult 9/27/2017 Dyslipidemia 8/16/2018 Open wound of abdomen 6/6/2019 Vancomycin-induced nephrotoxicity 6/25/2019 Debility 1/17/2022 OSA (obstructive sleep apnea) 1/17/2022
Andere Medikamente: acetaminophen 650-1,300 mg Oral EVERY 8 HOURS PRN albuterol sulfate 90 mcg/actuation 2 puffs Inhalation EVERY 6 HOURS PRN alcohol antiseptic pads TEST DAILY amlodipine besylate 10 mg TAKE 1 TABLET EVERY DAY. Patient taking differently:
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 2256704

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MI
Alter: 92,0
Geschlecht: M
Eingang: 28.04.2022
Impfdatum: 22.12.2021
Beginn: 27.04.2022
Tage bis Beginn: 126,0
Dosis: 3
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Asthenia C-reactive protein increased COVID-19 Comminuted fracture Computerised tomogram abnormal Computerised tomogram head normal Confusional state Cough Dehydration Dyspnoea Dyspnoea exertional Fall Gait disturbance Humerus fracture Hypophagia Impacted fracture Mental status changes Myalgia

Symptomtext

his is a 92-year-old male with a past medical history significant for coronary artery disease, DVT, GERD, subdural hemorrhage and craniotomy and cholecystectomy, who presents to the emergency department with complaints of progressive symptoms of cough, shortness of breath and altered mentation for approximately 1-1/2 days. This occurs in the setting of a recent fall. Patient was seen in the emergency department on 4/22/2022 for fall when he tripped while using his walker. The patient suffered a comminuted impacted fracture of the neck of the right humerus. Patient's radiographic studies in the emergency department on that day were x-rays of the shoulder as well as CT scans of the shoulder. He did not have any other scans of the head neck as he had denied any head injury no loss of consciousness. Patient has presently a nonproductive cough shortness of breath and increased dyspnea on exertion and per the son is more confused

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Praegender Schweregrund: Dehydration
Hospital-Tage: 1,0
Labordaten: Problem 1: COVID-19 Plan 1: Patient presents with symptoms of confusion, generalized weakness, muscle ache, poor oral intake. No shortness of breath, cough, or fever reported. Patient was vaccinated for COVID-19. Plan: -Patient has significantly elevated C-reactive protein and ESR -We will start Solu-Medrol 40 mg twice daily. -Since the patient is not requiring oxygen so far, and there is no significant cough or fever, will hold remdesivir for now. -Gentle IV fluid hydration. -Tylenol for fever. -Patient is anticoagulated with Eliquis. Problem 2: Confusion Plan 2: Secondary to COVID-19 infection, and poor hydration. CT head is negative for acute intracranial pathology. -His mental status is improving. -Gentle IV fluid hydration as above. Problem 3: Generalized weakness Plan 3: Secondary to viral infection. Hydration and pain control as above. -We will obtain OT/PT evaluation. Patient lives with his son. He might need short-term rehab. He had a recent fall with a fracture of the right humeral neck that is requiring sling for now. Problem 4: Closed fracture of right humerus Plan 4: Secondary to a fall. His son describes a mechanical fall happened at the backyard. Patient was seen by orthopedics, had CT scan that showed impacted fracture. Recommendation was to use a supporting sling and immobilization. -Optimize pain control. -OT/PT evaluation Problem 5: History of DVT (deep vein thrombosis) Plan 5: Patient is on Eliquis. We will continue during this hospitalization Problem 6: History of hypothyroidism Plan 6: Interestingly the patient is on levothyroxine and liothyronine not sure why. We will resume home medication Problem 7: Coronary artery disease without angina pectoris Plan 7: Patient has a history of coronary artery disease and 1 stent. He is on Plavix which will continue. There is no chest pain. Problem 8: OSA on CPAP Plan 8: Continue nocturnal CPAP same home settings
Aktuelle Erkrankungen: unknown
Vorgeschichte: hypothyroidism CAD/angina GERD CRF sleep apnea HTN diabetes
Andere Medikamente: Current Home Medications 1. Coenzyme Q10 200 mg oral capsule : 1 tab(s) orally once a day 2. dorzolamide-timolol 2%-0.5% preservative-free ophthalmic solution : 1 drop(s) to each affected eye 2 times a day 3. Eliquis 2.5 mg oral tablet : 1
Allergien: contrast dye
Vorherige Impfungen: -

VAERS 2250633

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

moderat

Staat: NY
Alter: 49,0
Geschlecht: F
Eingang: 25.04.2022
Impfdatum: 22.02.2022
Beginn: 23.02.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Headache Hypertension Pyrexia

Symptomtext

high blood pressure, heaaches, chills, fever

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: asthma, graves disease
Andere Medikamente: -
Allergien: eggs
Vorherige Impfungen: -

VAERS 2195166

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 23.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Burning sensation Chest pain Chills Condition aggravated Dizziness Facial paresis Fatigue Feeling abnormal Feeling hot Head discomfort Headache Hypoaesthesia Immediate post-injection reaction Increased appetite Muscle spasms Muscular weakness Myalgia

Symptomtext

immediatly after administration left am warm, numb in hand mild chills mild headache, increased heatrate AP110 through night lightheaded, muscle aches chest pain. next day burning sensatin left arm chllls. since Feb 24th daily headahes pulsatin. pressure left occipital and frontal, temporal region, brain fogginess, lightheaded, chills and fatique,occaional numbness, face arm and muscle weakness. month later toe crampin. continue with Ongoing daily headahes left occipital , frontal and temporal, brain fog 5 weeks in

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Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Covid positve 1/21/2022. symptoms of sore throat and chills, sneezing 2 days. otherwise nasal congestion felt like head cold
Vorgeschichte: hypothyroid
Andere Medikamente: levothyroxine, vitaminc,vitamin d
Allergien: prednisone
Vorherige Impfungen: moderna 01/20/21

VAERS 2192064

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 52,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 04.02.2022
Beginn: 04.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arrhythmia Arthralgia Dysphagia Extrasystoles Eye pain Heart rate increased Immediate post-injection reaction Injection site pain Laboratory test Lymphadenopathy Night sweats Ocular discomfort Oral contusion Petechiae Ultrasound scan abnormal

Symptomtext

Immediately as injection being administered felt burning form injection site to elbow. 4hours later had swollen lymph nodes to neck bilaterally and under jaw, unable to swallow. Temp 99.9 every joint in body aches. 8hours later had increased heart rate with any exercise( walking up stairs) Day1 still swollen lymph nodes and now with night sweats Day 2 now with pressure and pain behind Left eye- advised by employee health NP to see Ophthalmologist Day 3 Ophthalmologist was told it was likely secondary to swollen lymph nodes Day 5 went for thyroid sono - "shotty lymph nodes" Day 6 petechiae to bottom of feet, lymph node swelling decreased on right and under chin now able to swallow without difficulty Day 11 Bruising noted on tongue and under tongue 4weeks to the day arrhythmias- bigeminy trigeminy

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Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: 2/7/22 Ophthalmologist 2/9/22 Thyroid sonogram -> Shotty lymph nodes 3/1/22 lab work
Aktuelle Erkrankungen: -
Vorgeschichte: Hypothyroidism
Andere Medikamente: Synthroid
Allergien: pcn
Vorherige Impfungen: -

VAERS 2180183

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: VA
Alter: 57,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Hypertension Infection

Symptomtext

The day after getting the vaccine 12/21, I noticed my blood pressure was high so I went to urgent care. My blood pressure was 190/something. Urgent care gave me Lisinopril for one month. After that it went back to normal. It has come back up again recently but that could be due to an infection in my body.

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Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Vitamin C, Vitamin A, Calcium, Multivitamin
Allergien: Codeine
Vorherige Impfungen: past influenza shot, rash

VAERS 2165487

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MA
Alter: 69,0
Geschlecht: M
Eingang: 08.03.2022
Impfdatum: 22.12.2021
Beginn: 06.01.2022
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Condition aggravated Cutaneous vasculitis

Symptomtext

Patient developed a recurrence of cutaneous small vessel vasculitis affecting upper and lower extremities approximately 1-2 weeks after receiving COVID booster shot without other clear triggers. Of note, he has a history of known cryoglobulinemia secondary to prior hepatitis C infection with previous episode of cutaneous small vessel vasculitis (viral infection since treated and cleared but with persistent cryoglobulins.)

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: cryoglobulinemia
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2147169

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: CA
Alter: 51,0
Geschlecht: F
Eingang: 26.02.2022
Impfdatum: 12.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / OT

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Anxiety Fatigue Feeling abnormal Headache Nausea Palpitations Rash Tremor Visual impairment

Symptomtext

Initially, the day after in the evening, the beginning of fatigue and nausea along with a minor headache. Day 3 was the worse with all 3 of these. These all seemed to correct themselves. About a week later, I started noticing: continued fatigue here and there but now also heart palpitations, brain fog (remembering things, words, stumbling over words), worsening internal vibrations to shakiness (jitters) developing in toes and legs, abdomen, vaginal area, rear end, and head area along with eye twitching and vision issues and not feeling like myself/anxious. Vibrations were not as bad before and not moving around. Lastly, a couple of strange bumps on my skin - arm, chest area - allergic reaction? Though this many weeks later, the bumps remain. These symptoms are similar to my experience to 2nd dose. See past filing. That would be helpful. I can't believe I'm back to this again. Much had improved and now I'm taking a step backwards again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: I have not had any. I'm scheduled in March to take a blood test, as normal part of my care. Maybe something will show up there? I also will, hopefully, see my new general doctor. My last doctor resigned her position in the fall and do not have a new general yet. I am seeing a gastro dr to look more closely at the vibrations, thankfully, since the booster they are only worse and moving around more. Maybe I should not have had booster with all symptoms not completely gone from 2nd dose? A good warning or better undertstanding of informed consent to patients would be appreciated, as we're going by recommendations.
Aktuelle Erkrankungen: 2nd Moderna dose 5/2/21 was reported., you should have on file. It took me about 3 months or so to recover and was hesistant but being pushed to get this booster as a public school teacher.
Vorgeschichte: My body had been healing from explant of implants that made me terribly and chronically sick, breast implant illness. Removed implants 8/2019. Interesting, the vaccine seems to caused a similar type of foreign object issue to my immune system yet I've had vaccines in the past. What is in this vaccine that is that different causing concerning issues to my body and lifestyle? Better warning must be provided to consenting adults as to all the possibilities of what can go wrong. I wasn't provided with proper informed consent. I'm only learning of those with similar issues as I'm trying to explore how to get my health back. It should not be this way.
Andere Medikamente: vit d, omega 3, multi, probiotic
Allergien: septra and morphine
Vorherige Impfungen: -

VAERS 2131552

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 18.02.2022
Beginn: 20.02.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Hyperhidrosis Lymph node pain Lymphadenopathy Oedema peripheral Pain Paraesthesia

Symptomtext

Received Covid-19 booster on 02-18-2022 at 12:25pm. I felt many chills, sweats and body aches throughout Saturday 02-19-2022. At around 5am on Sunday 02-20-2022 I was awakened by a pinching sensation in left axilla (vaccination had been to left deltoid)-found an area of swelling approx. 3 inch oval painful lymph node. Monday morning 02/21/2022 the lymph nodes to left clavicle and lateral neck swollen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None presently- pending answer from MD.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: cephalosporins
Vorherige Impfungen: Thyroid and Hormonal fluctuations from March 2021 (after Moderna vaccinations #2 for Covid-19) until November 2021.

VAERS 2129808

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: OH
Alter: 34,0
Geschlecht: F
Eingang: 21.02.2022
Impfdatum: 08.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Dyspnoea Feeding disorder Headache Migraine Nausea Photophobia Tachycardia Tremor

Symptomtext

increased headache and migraine frequency, increased severity of migraines, inability to treat migraine with medication for relief, increased and worsening secondary symptoms of migraines (worse nausea, new tremors, new tachycardia, worse shortness of breath, worse light sensitivity, inability to eat due to worse nausea)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Migraines, anemia, vitamin D deficiency
Vorgeschichte: Migraines, anemia, vitamin D deficiency
Andere Medikamente: Vitamin D, Sprintec (which is not the cause of the reaction)
Allergien: cashews, bell peppers, metal, adhesive tape
Vorherige Impfungen: prolonged site pain and swelling due to metal allergy

VAERS 2121265

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: CA
Alter: 49,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 08.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Audiogram abnormal Cough Deafness neurosensory Dyspnoea Hypoacusis Tinnitus

Symptomtext

First week to week 4 of cough and SOB. Not relieved by any cough syrup. Was tested for COVID 19 twice within the period. WAs treated by prednisone 10 mg daily x 5days. Week two after the Vaccine noticed a distorted , vibration and echo on high pitchsound on the left ear, reduced hearing compared when receiving calls between the left and right ear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Audiological test result- mild to moderately-sever reverse sloping sensorineural hearing loss 2/16/22
Aktuelle Erkrankungen: none
Vorgeschichte: asthma
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2119459

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 16.02.2022
Beginn: 16.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Palpitations Sensation of foreign body

Symptomtext

lump in throat, palpatations

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: asthma
Andere Medikamente: -
Allergien: sulfur
Vorherige Impfungen: moderna 3/10/2021

VAERS 2119405

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MI
Alter: 50,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 01.02.2022
Beginn: 08.02.2022
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Headache Nausea Pain in extremity

Symptomtext

pt states that her left arm and chest were sore for a couple of days after getting her covid vax. About 8 days later she developed severe headaches that make her nauseated. These symptoms would come and go. She still has these symptoms at this time and will contact her PCP.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HIV, COPD,
Andere Medikamente: Descovy 225mg, Tivcavy 50mg, Incruse Inhaler, Topirmate 50mg, Flovent Inhaler, Eliquis 2.5 mg, hydrocodone 3.25 mg, Vitamin D3, Zinc 50mg, B12 1000, Vitamin C 500mg, Sucralfate 1gm, 81 mg aspirin,
Allergien: erythromycin, fentanyl, penicillin, Pepcid, tomatoes,
Vorherige Impfungen: -

VAERS 2115257

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: CA
Alter: 22,0
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 22.01.2022
Beginn: 23.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test abnormal Chest pain Computerised tomogram Dyspnoea Electrocardiogram abnormal Heart rate increased Inflammation Influenza like illness Lymphocyte count increased Malaise Myalgia Peripheral swelling Rash Scan with contrast Vitamin D decreased

Symptomtext

Initial symptoms in the first 24 hours matched with prior exposures to the vaccine. Significant arm swelling, a small rash, and muscle aches. The trend changed after 24 hours. In prior exposures, influenza-like/COVID-19-like symptoms lasted for up to 12 days. In this exposure, none of these symptoms was present. Instead, muscle aches worsened significantly, Vitamin D levels dropped to dangerously low levels, heart rate became increased, and chest pain was present upon exerted movements such as getting out of a chair. The chest pain resolved after 4-5 days but breathless has remained to the present day that impacts day to day exertions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 1/23/2022: EKG was performed to evaluate heart function. No dangerous issues with rhythm were found outside of increased pressure. 1/31/2022: A full blood panel was performed that noted a sudden sharp decline in Vitamin D, slight elevation in Lymphs, and substantial inflammation in both arms noted by the phlebologist. 2/10/2022: A CT scan was attempted with contrast to further evaluate the situation. The scan was terminated after a vein burst with contrast after initial swelling after the contrast was administered. Pending further evaluation on the cause.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Allergic to Boostrix, minor allergy to gluten and egg cultures.
Vorherige Impfungen: severe reaction toDTaP, approx 2005 or earlier, unknown, unknown. Lesser reaction to Tdap, unknown, unknown, likely Boostrix

VAERS 2110266

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 34,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 19.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Dyspnoea Palpitations

Symptomtext

Did not notify employer, posted on Facebook that she had heart palpitations and shortness of breath that started 16 hours after vaccination, but also stated that she had similar episodes two weeks prior to vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Unknown
Aktuelle Erkrankungen: anemia, thyroid, arthritis, anxiety, depression
Vorgeschichte: anemia, thyroid, arthritis, anxiety, depression
Andere Medikamente: Synthroid
Allergien: Wellbutrin, progesterone
Vorherige Impfungen: -

VAERS 2110236

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 26,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 11.02.2022
Beginn: 11.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Anxiety Dyspnoea Flushing Heart rate increased Hypertension

Symptomtext

Patient began complaining of feeling flushed and high HR 127 and high BP 167/100 30 minutes after receiving vaccine. Stated she had been having this issue intermittently since her second covid vaccine dose. Stated she was anxious and sob. Was taken to ER and then later that night at 2330 she went to ER for the same symptoms where "she got a shot in her butt to calm her down" She is seeing her PMD 2/14/22 at 1530.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: unknown
Aktuelle Erkrankungen: bronchitis, intermittent heart palpations since second dose covid vaccine.
Vorgeschichte: 3 c section, gb removed
Andere Medikamente: not known
Allergien: nka
Vorherige Impfungen: States has had heart palpitations since receiving second covid vaccine dose.

VAERS 2099726

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: PA
Alter: 73,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 16.01.2022
Beginn: 23.01.2022
Tage bis Beginn: 7,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Condition aggravated Erythema Musculoskeletal stiffness Peripheral swelling Pruritus

Symptomtext

Patient reported that her right arm swelled, became stiff, red, and itchy about one week after administration of Moderna. She called her doctor who advised her to apply ice and use Aleve and Claritin. She stated the issue was mostly resolved at this point (approximately two weeks after development). She did not want to receive the second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Patient stated something similar happened with the tetanus vaccine.

VAERS 2092844

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 59,0
Geschlecht: M
Eingang: 07.02.2022
Impfdatum: 28.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Rash

Symptomtext

This was a BOOSTER dose administered on 12/28. Patient reports onset of rash to primarily the bilateral shins. Not worsening, non-itching, no pain, no burning, no changes. Of note, patient had a visit on 11/10 describing similar rash, however he denied the appearance of the rash until the booster. No fever, chills, no nausea/vomiting, no changes in appetite.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None. Patient prescribed triamcinolone 0.1 % topical
Aktuelle Erkrankungen: -
Vorgeschichte: Intellectual disability Allergic rhinitis Anxiety Esophageal reflux Mixed hyperlipidemia Pain in joint, shoulder region Mild intermittent asthma High Attention to Health Literacy Microhematuria Barrett's esophagus Emergency Room Frequent User Blister of toe of left foot without infection
Andere Medikamente: ALBUTEROL SULFATE (VENTOLIN HFA) 108 (90 Base) MCG/ACT Inhalation Aero Soln Atorvastatin Calcium 10 MG Oral Tab Cetirizine HCl 10 MG Oral Tab cyclobenzaprine 10 MG Oral tablet (Expired) Loratadine 10 MG Oral Tab Olopatadine HCl 0.1 % O
Allergien: Codeine Phosphate
Vorherige Impfungen: -

VAERS 2083275

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: UT
Alter: 52,0
Geschlecht: M
Eingang: 03.02.2022
Impfdatum: 01.01.2022
Beginn: 31.01.2022
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dyspnoea Pharyngeal swelling Pruritus Rash Urticaria

Symptomtext

**Moderna Booster** On day 10 after my booster, I started to have the following symptoms: Itchy skin all over. Skin rash/hives if the skin was itched or scraped. Swollen throat which made it hard to breathe, but was not enough to require medical intervention.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Fish. Seafood. Penicillin.
Vorherige Impfungen: -

VAERS 2076122

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MA
Alter: 71,0
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 19.01.2022
Beginn: 19.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Chills Computerised tomogram thorax abnormal Cough Diarrhoea Dyspnoea Dyspnoea exertional Headache Lethargy Malaise Myalgia Inflammation Vaccination complication Nausea Orthopnoea Pyrexia

Symptomtext

Patient had her moderna COVID booster on 01/19, after which she developed generalized malaise, lethargy, constant holocranial headache, myalgias (UE), chills, subjective fever, dry cough, nausea, no emesis, SOB, DOE, orthopnea, 2 loose BMs, denies increasing LEE. She started taking two tylenol every 3 hours with no relief of symptoms. Her home sats 89-90% so daughter suggested she go to urgent care. In urgent, she was satting 85% off O2 so referred to ED on 1/23. CT chest concerning for post COVID organizing PNA v. ILD flare. Reassuringly, her O2 requirement has weaned to 1L NC and she is saturating well. prednisone 60mg daily (1/30), s/p solumedrol 500mg daily (1/27-1/29), solumedrol 250mg BID (1/26), prednisone 1mg/kg/d (1/25), dexamethasone x 1 (1/24) - S/p ceftriaxone 1g daily / azithromycin 500mg daily x 7 days (1/25 - 1/31)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: covid-19 requiring hospitalization (12/21-12/26)
Vorgeschichte: atrial fibrillation/flutter, heart failure preserved ejection fraction, endometrial cancer, morbid obesity, depression
Andere Medikamente: albuterol, apixaban, atorvastatin, gabapentin, robitussin, melatonin, metoprolol tartrate, ondansetron, spironolactone, tamoxifen, trospium, venlaxafine
Allergien: taxol, latex, bupropion, felodipine, lisinopril; tipiramate
Vorherige Impfungen: -

VAERS 2082274

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: GA
Alter: 69,0
Geschlecht: M
Eingang: 02.02.2022
Impfdatum: 10.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Glycosylated haemoglobin increased Neuropathy peripheral

Symptomtext

Patient stated after he took the initial shot of the series, his neuropathy got slightly worse. After the second dose, patient stated his neuropathy got really bad. After the booster, the pain was the worst it had been. His nurse practitioner told him to increase his gabapentin. He was prescribed a sleeping pill. He states his hemoglobin A1C increased from 5.5 to 6.5.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: Lyme disease, diabetes, neuropathy
Vorgeschichte: Lyme disease, diabetes, neuropathy
Andere Medikamente: Gabapentin, Metformin, Temazepam, CBD, Tylenol, Advil, Marijuana
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2069258

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 27.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Dysphagia Dyspnoea Pruritus

Symptomtext

Patient had generalized itchiness for a few minutes after her Moderna booster shot. Also, patient verbalized difficulty of swallowing and some SOB.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Allergic reaction to dye
Vorgeschichte: Sleep apnea, COVID-19 PNA, anaphylaxis, congenital heart defect, persistent vena cava
Andere Medikamente: Benadryl 150mg PO (prior to her vaccine)
Allergien: Adhesive Tape, Sulfa, Iodine dye, Aspartame
Vorherige Impfungen: Itchiness.

VAERS 2068799

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MA
Alter: 23,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 28.12.2021
Beginn: 09.01.2022
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Chest X-ray Chest discomfort Chest pain Dysphagia Electrocardiogram Influenza virus test negative Injection site erythema Injection site mass Injection site pain Injection site pustule Rash erythematous SARS-CoV-2 test negative Urticaria

Symptomtext

I received the vaccine on December 28, 2021. I started to notice symptoms of a red rash / hives spread on my back neck chest area on Sunday, January 9 and I took Claritin. The rash continued to get worse and popping up in random spots on my body even while taking Claritin or Benadryl. By Tuesday, December 11 I started to have chest pains too. Feeling like squeezing sensation in the middle of my chest behind my breast bone also felt hard to swallow and like something was stuck in my chest. The chest pains continued through Wednesday until it got bad enough to go to the ER early in the morning on Thursday, January 13. At this point I had also noticed the injection site had become red with pus and had a small lump under it that was tender to the touch. Upon my visit they performed an EKG 12 lead imaging test as well as a chest x-ray and some bloodwork which came back normal. They believed it was likely all the symptoms could be allergic reaction from booster they thought that chest pain may be pericarditis and to treat with 600 mg of ibuprofen every six hours for two days and also acid reflex and to take over-the-counter anti-acid like Tums. For the postulate they started a five day course of antibiotics of 100Mg doxycycline hyclate. For the rash they prescribed 50 mg tablets of prednisone for four days and also instructed to take 10 mg of Zyrtec three times a day and 20 MG of Pepcid as well as Benadryl until it goes away. Chest pain symptoms seem to improve with these regimen however the rashes and hives continued. The prescriptions finished on Monday January 17th. I had an already scheduled appointment on Tuesday the 18th with a dermatologist who noted all the information and instructed to continue using the Zyrtec 2 times a day. By Tuesday night the chest pains returned and continued to become worse and I reached out to the doctor and she prescribed another round of prednisone taper to help with the allergic reaction. I started that on Thursday Jan. 20th and chest symptoms began to improve immediately however rashes still pop up randomly. At this point in time the steroids seem to keep the chest pain at bay however the rashes keep popping up and it seems more now that whatever touches my skin leaves a mark. The steroid prescription will be done on February 1 and I have a follow up doctor appointment on 31 January to review everything.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: The tests performed at the ER include a 12 lead EKG test and chest x-ray both of which came back normal. A coronavirus and influenza a and B swab were taken none were detected. They performed bloodwork a lavender top and a troponin test to make sure the cardiac enzyme level were appropriately negative. All performed on January 13th, 2022
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: B12, Calcium, magnesium, omega 3, muti vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2065256

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

moderat

Staat: NY
Alter: 72,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Injection site pain Injection site swelling Limb injury Paraesthesia Product administered at inappropriate site

Symptomtext

Site: Pain at Injection Site-Severe, Site: Swelling at Injection Site-Medium, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Additional Details: patient says shot was given too high and thinks it was given in the bursa, this has caused a lot of sweeling and pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2062184

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

moderat

Staat: PA
Alter: 28,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Migraine Nausea Retching Vomiting

Symptomtext

Extreme nausea and vomiting, with migraine, lasting 38 hours after the vaccine was administered. Took Dramamine to help with nausea, but continued dry heaving for the next 2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: no
Andere Medikamente: Daily Rx of: Lamotrigine 150mg Bupropion 300mg Tri-Sprintec birth control Dramamine when home from vaccination
Allergien: no
Vorherige Impfungen: Moderna vaccines 1 and 2, constant vomiting for 48-36 hours

VAERS 2057398

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

moderat

Staat: VA
Alter: 23,0
Geschlecht: M
Eingang: 22.01.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Asthenia Chest discomfort Chest pain Chills Dizziness Fatigue Flushing Hyperhidrosis Lethargy Pyrexia

Symptomtext

Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Chills-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Weakness-Medium, Additional Details: patient stated that he had a similar reaction to his first shot but not his second shot. patient says his reaction to the first shot went away in 30 minutes after he took enough rest. patient states he works in a healthcare setting ,and he is well aware of his reactions. patient declined the use of diphenhydramine. patient's bp was 118/79,and heart rate 73 when he left the store. patient got better after 1 hour of event.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2054626

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MA
Alter: 37,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 22.12.2021
Beginn: 06.01.2022
Tage bis Beginn: 15,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Facial pain Feeling hot Hypoaesthesia Hypoaesthesia oral Paraesthesia Pruritus Skin exfoliation Swelling face Swelling of eyelid Urticaria

Symptomtext

Two weeks after my booster Moderna shot, I suddenly had symptoms like hives, itchy and red skins of my upper body, neck and face. One day later, my face and eyelids became very swollen. Then whenever I felt hot, parts of my body skin felt acupuncture from hundreds of small needles. After 4-5 days, my swollen face and eyelids got better and my face skin were peeling. Then my upper lip became numb and tight. My left half face feel less painful when pinched by fingers than the other right face. The numbness of my lip and half face are still existing, and have lasted for 10 days now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: I have been taking claritin and zyrtec, and methylcobalamin?B12?for about 10 days.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: vitamin C, D and zinc occasionally
Allergien: only allergic to pollen in the spring before taking any Covid vaccination shots, and then became allergic to peaches suddenly after two vaccination shots.
Vorherige Impfungen: -

VAERS 2051049

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: SC
Alter: 27,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 09.01.2022
Beginn: 09.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Bedridden Chest pain Chills Decreased appetite Headache Impaired work ability Pain in extremity

Symptomtext

Headache - 3 days Chills - 1 day Lack of appetite - 2 days Severe chest pain (almost went to hospital. Had to sleep with a heating pad inside my shirt) - 2 days Left arm pain - 4 days Missed work for 1 day. Completely bedridden that day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Gerd. Depression.
Andere Medikamente: Paxil
Allergien: None
Vorherige Impfungen: -

VAERS 2047677

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: OH
Alter: 37,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 07.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest discomfort Chest pain Dyspnoea exertional Electrocardiogram normal Neck pain Pain Paraesthesia Stress echocardiogram normal Troponin normal

Symptomtext

Left sided chest pain- squeezing sensation, radiating to neck and down left arm, tingling left arm, with shortness of breath on exertion x several days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: ER visit - EKG was normal, serial troponin negative, Stress ECho reported normal with EF 55%, (however pt on lisinopril for several years) Date of test 01/13/22
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension
Andere Medikamente: Lisinopril 10mg/day, cetrizine 10 mg/day, vitamin D 2000 IU per day
Allergien: none
Vorherige Impfungen: -

VAERS 2045472

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: OH
Alter: 38,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest discomfort Chest pain Chills Diarrhoea Fatigue Heart rate increased Injection site pain Lethargy Pain Paraesthesia Pruritus Rash Tachycardia Tinnitus

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Itch Generalized-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Chest Tightness / Heaviness / Pain-Medium, Systemic: Chills-Medium, Systemic: Diarrhea-Medium, Systemic: Exhaustion / Lethargy-Mild, Systemic: Tachycardia-Mild, Systemic: Tingling (specify: facial area, extemities)-Medium, Systemic: Tinnitus-Mild, Additional Details: Tingling in finger tips of vaccinated arm, moved to other hand as well. Pt given benadryl and was feeling better. At home symptoms continued and pt took more benadryl. At home had slight increase in HR, tinitus at bedtime, chest tightness and rash on both arms and neck. Pt called PCP and was instructed if symptoms worsened to go to ER. Pt has f/u with PCP next week. As of today, pt has not been seen in ER, but continues to self medicate with benadryl.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2043785

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: IL
Alter: 45,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Mobility decreased Pain Pain in extremity Periarthritis

Symptomtext

Patient got Moderna booster on Wednesday. Severe arm pain started appox 3 hours later. Patient concernd that the needle may have nick/hit the nerve. Patient expected arm to be sore but this was much more severe. she described an episode of frozen shoulder where she was unable to move it for a period of time. Also had pain shooting from the area to elbow down to wrist and sometime to fingertips of pointer and thumb. The episode started 3 hours after injection and lasted 12 hours. She was still having some trouble doing some movement 5days later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None yet. Patient has reached out to her PCP
Aktuelle Erkrankungen: None known
Vorgeschichte: Allergic rhinitis GERD
Andere Medikamente: Montelukast 10mg po daily Albuterol MDI QID prn
Allergien: Sulfa drugs - rash
Vorherige Impfungen: -

VAERS 2043426

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NC
Alter: 46,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 13.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Amnesia Dyspnoea Fatigue Feeling abnormal Heart rate increased Hyperhidrosis Hypoaesthesia Nasal congestion Nausea Palpitations Pyrexia

Symptomtext

My heart rates is up and I have general fatigue and shortness breath. I experienced nausea, high fever and sweats. I had numbness on the left side of face. Brain felt fuzzy. It all started to hit me at night and the nausea and palpitations are currently bothering me a lot. I have a stuffy nose memory loss.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Anxiety/Depression
Andere Medikamente: Prozac, Hydroxyzine, Tylenol
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2043021

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 58,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 12.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Palpitations

Symptomtext

Heart palpitations

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, diabetes
Andere Medikamente: Humalog, Nadolol, Hydrochlorothiazide, losartan potassium, rosuvastatin, low dose aspirin, multi vitamin.
Allergien: None
Vorherige Impfungen: -

VAERS 2042810

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 31.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Chest pain Chills Electrocardiogram Fatigue Irritability Pain Pain in jaw

Symptomtext

Ever since I had the Moderna booster I have been randomly experiencing occasional chest pain, chills and body aches, lower jaw(tooth) pain, fatigue and irritability.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: I visited a cardiologist on 1/3/22. EKG came back fine. He sent me for a full blood panel. All blood work came back within normal range with the exception of cholesterol On 1/26/22 I will return to cardiologist for Ultra sound and stress test.
Aktuelle Erkrankungen: -
Vorgeschichte: Born with one kidney. Birth Defect (missing right kidney, ovary, and tube.
Andere Medikamente: multi Vitamin, B complex, Vitamin D, Echinacea, zinc
Allergien: Iodine, shellfish, propofol, spider bites
Vorherige Impfungen: had pfizer shots on 3/29/21 and 4/20/21 and had severe flu-like symtoms for 2 days to each vacine

VAERS 2037801

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: GA
Alter: 22,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: 11.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Erythema Lymphadenopathy Migraine Peripheral swelling Pyrexia

Symptomtext

FEVER, MIGRAINE, ARM REDNESS AND SWELLING, ENLARGED LYMPH NODES UNDER LEFT ARM; TREATED WITH BENADRYL AND ADVIL; EVENTS STOPPED 1/14/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2036612

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 33,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 10.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypersensitivity Injected limb mobility decreased Injection site erythema Injection site inflammation Injection site pain Injection site pruritus Injection site swelling Injection site warmth Lymphadenopathy

Symptomtext

Immediate itching from shot. A 4?x4? swollen, painful red circle from injection site by time I got home <45 mins after shot. Following day couldn?t comfortably lift arm from swelling, couldn?t lay on side from pain and swelling, swollen area still 4?x4? hot and red. Also swollen lymph nodes in armpit and neck on side of injection. Decided to write to my doctor that night about 36 hours after shot to see what I can take and if this is normal. He wanted to see me via telemedicine- this was 1/12/22. Looked at my arm and declared it an allergic reaction and worried about it turning into cellulitis. Said it?s hard because he?s diagnosing over webcam but can see how large and inflamed it is. By 48 hours pain has subsided and itching has ramped up. He prescribed doxycycline hyclate 100 mg/ 2 day for 7 days to be safe and start taking Benadryl or 24 hour allergy pills. I started Benadryl since it?s what I had at home. I?m instructed to call if no change by Friday. Start the doxycycline and Benadryl regimen Wednesday night. Thursday reaction starts to fade, decrease swelling, continue itching. Friday is faintly still red, swollen and still itching.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injected limb mobility decreased
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Duloxetine HCL DR 20 mg
Allergien: No
Vorherige Impfungen: -

VAERS 2028791

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NM
Alter: 35,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 05.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Back pain Blood test Chest X-ray normal Chest pain Dizziness Dyspnoea Electrocardiogram Electrocardiogram normal Heart rate increased Palpitations Tachycardia

Symptomtext

Chest pain on left side of chest and under left shoulder blade. Lightheaded, shortness of breath, resting heart rate in the 130's, and when I would walk, it would shoot up to the 160's. Dizzy, heart pounding, trouble breathing. Went to an urgent care that wouldn't see me, but they asked which vaccine I had because they had multiple people come in after their booster shots with those same symptoms. Went to another urgent care, they did an EKG, and chest xray and both were clear. they were highly concerned about the tachycardia, so they sent me to the emergency room. At the ER they did another EKG, and blood work to rule out a blood clot in my lungs. They could not figure out why my heart rate was still so high, when my blood pressure, temp and everything else was normal. They gave me fluids, ibuprofen, and something to calm my heart down (i dont remember the name) and told me that I needed to follow up with a cardio doctor to check my heart out.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: 2 EKGs, chest xrays, and blood work to check for blood clots
Aktuelle Erkrankungen: no
Vorgeschichte: Ulcerative colitis, depression/anxiety, insomnia
Andere Medikamente: venlafaxine, clonazepam, amitriptyline
Allergien: no
Vorherige Impfungen: -

VAERS 2028385

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: PA
Alter: 58,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 01.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Acoustic stimulation tests Condition aggravated Deafness unilateral Magnetic resonance imaging head Tinnitus

Symptomtext

Tinnitus and more hearing loss in my left ear,taking Flucicasone propionate nasal spray and waiting to see if there is any relief.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: MRI of head to rule out anything physical,also hearting tests to evaluate amount of hearing loss to compare with a test taken 2 weeks prior to vaccine
Aktuelle Erkrankungen: cold
Vorgeschichte: thyroid disease,mild hearing loss in my left ear
Andere Medikamente: Synthroid,Livalo,Omeprazole,muti vitamins,vit D ,culterelle
Allergien: none
Vorherige Impfungen: -

VAERS 2006474

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Dizziness Headache Hypertension

Symptomtext

Dizziness, HTN, pounding sensation to right eye and head

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Ulcerative colitis
Andere Medikamente: Lialda, Zyrtec
Allergien: -
Vorherige Impfungen: -

VAERS 2001388

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: VA
Alter: 31,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 03.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Dysgeusia Injection site swelling Taste disorder

Symptomtext

Unable to taste other than metallic taste, moderate to severe swelling at injection site, resolving left sided chest pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None.
Vorgeschichte: Barrets esophagus, stomach ulcer, depression, anxiety.
Andere Medikamente: Zoloft; Claritin; Adderall; Pantoprazole.
Allergien: None.
Vorherige Impfungen: Covid vaccine 5/7/21, arm and neck pain, nothing severe.

VAERS 1999840

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: CA
Alter: 64,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 18.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Vertigo Vertigo positional

Symptomtext

Vertigo starting within 24 hours and continuing through today 1/3/2022. Was severe on Day 3 post vaccine and has improved gradually but I continue to be unable to put my head down below my waist without initiating vertigo. This symptom was present with the first two vaccines but has worsened with each additional vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Obesity, hypertension
Andere Medikamente: metoprolol 50 mg
Allergien: perfume
Vorherige Impfungen: 1/16/21 Moderna and 2/13/21 Moderna had less severe symptoms of vertigo, Each vaccine has increased to severity and length of ti

VAERS 1997868

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: MA
Alter: 31,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 19.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain

Symptomtext

Abnormally severe chest pain around the general heart area. On-going ?chest? pains. Not related to diet or acid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Lisinopril, tobacco smoke, latex
Vorherige Impfungen: -

VAERS 1989105

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

moderat

Staat: OR
Alter: 36,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 26.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

Chest discomfort Chest pain Dizziness Dyspnoea Fatigue Hypertension Lethargy Pain Tachycardia

Symptomtext

Systemic: Allergic: Difficulty Breathing-Severe, Systemic: Body Aches Generalized-Severe, Systemic: Chest Tightness / Heaviness / Pain-Severe, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Hypertension-Severe, Systemic: Tachycardia-Severe

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1989101

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21A

moderat

Staat: TX
Alter: 22,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 27.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Hypoaesthesia Pain Paraesthesia

Symptomtext

Systemic: Numbness (specify: facial area, extremities)-Medium, Systemic: Tingling (specify: facial area, extemities)-Medium, Additional Details: Patient complains of radiating numbness/tingling down left arm and up the left/back side of her neck, often followed by pain. Review of injection site reveals the poke was not too low or high. Started 12/28 (day after injection) and continuing into today 12/29.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1981942

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: TX
Alter: 32,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 22.12.2021
Beginn: 25.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dyspnoea Eyelid ptosis Fatigue Headache Pain Vertigo

Symptomtext

Pt. states that after receiving the 3rd dose of Moderna 12/22/2021, started experiencing symptoms 12/25/2021 pain of the right side of the back side of the head, fatigue, shortness of breath, vertigo, and droopy eyes. Self-treating with Tylenol for pain, no noted Primary visit/communications. Still continuing to experience symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Multi-Vitamin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1981941

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NY
Alter: 41,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 21.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest pain Fatigue Heart rate abnormal Heart rate decreased Heart rate increased Pain in extremity Palpitations

Symptomtext

I had a sore arm initially and then on Wednesday I felt really tired in the morning. My heart started pounding at around 7 or 8pm and heart rate was 100 which is abnormal for me. It stopped after I spoke with the provider but started again that night and has been ongoing since. I started having pain in my chest and the palpitations are off and on. Heart rate when at rest is usually mid 70's but its been remaining in the 80's and then last night. my heart rate dropped to the 60's.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Ibuprofen; Advil Cold and Sinus
Allergien: Clindamycin Zithromax Amoxicillin
Vorherige Impfungen: -

VAERS 1981579

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: TX
Alter: 30,0
Geschlecht: M
Eingang: 27.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Burning sensation Chest X-ray Chest pain Chronic inflammatory demyelinating polyradiculoneuropathy Differential white blood cell count Discomfort Dyspnoea Electrocardiogram Fatigue Metabolic function test Troponin I

Symptomtext

Moderate chest pain that began early the morning after the COVID-19 Moderna booster. The chest pain was located on the left pectoral with chest pain, shortness of breath, and fatigue symptoms. Patient went to the ER at 7am on 12/21/2021 and received an ECG which showed normal vitals. Patient was diagnosed with 'chest wall pain' and sent home. Patient continued to monitor symptoms throughout the week, which persisted at around the same pain level. Patient alternated doses of Tylenol and Aleve for pain and notes that the pain persisted. Patient notes that the pain is centered around the sternum, and feels like a tight/burning sensation that is uncomfortable and creates difficulty breathing. On 12/26/2021 the patient returned to the ER with the same chest pain symptoms as earlier in the week. Patient had blood tests performed, which returned negative for anything heart related, and was diagnosed with Nonspecific Chest Pain. Patient was prescribed methocarbamol and directed to a cardiologist for a follow up appointment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: CBC w/ Auto Differential, Comprehensive Metabolic Panel, Troponin I (High sensitivity), ECG 12-Lead, ECG 12-Lead Interpretation, XR Chest 1 View
Aktuelle Erkrankungen: mild paronychia on left middle finger nail bed
Vorgeschichte: none
Andere Medikamente: none
Allergien: Nickel
Vorherige Impfungen: -

VAERS 1980871

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: -
Alter: 42,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 23.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Palpitations

Symptomtext

Noticed heart palpitations on the day after vaccine (about 24 hours later). Don't remember noticing on day of vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1974729

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: -
Alter: 39,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abnormal dreams Fatigue Headache Hypersomnia Inappropriate schedule of product administration Injection site paraesthesia Lymphadenopathy Myalgia

Symptomtext

I got my COVID vaccine booster (Moderna). This was 7 months after completing my first 2 doses of the Pfizer COVID vaccine. After 12 hrs I started feeling extreme fatigue, muscle aches, headache and my left arm (site of injection) was tingling. I basically slept the entire day after the vaccine which wasn't restful because I was experiencing very vivid dreams. The extreme fatigue ended after approximately 24 hrs but the muscle aches continued for 48-72 hrs. Additionally, 36 hours after vaccination there was swelling in my left arm pit, likely lymph nodes, which is still persisting. Also, I experienced a lot of night sweating the second night after my vaccine; I woke up completely drenched in sweat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1971349

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: TX
Alter: 29,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Condition aggravated Headache Injection site mass Injection site pruritus Injection site swelling Injection site urticaria Oropharyngeal pain Pain Pain in extremity Pyrexia Tenderness Urticaria

Symptomtext

Within 2 hours of vaccine: Itchy hives on injection site, hives on neck and chest. Within 12 hours of vaccine: hard golf ball sized lump and swelling on injection site, severe arm pain, fibromyalgia flare (pain and tenderness on entire body), fever, headache, sore throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia, HSV-2, Hypothyroidism, Chronic Migraine Disorder.
Andere Medikamente: Levothyroxine, Lamotrigine, Klonipin, Slynd, valacyclovir
Allergien: No
Vorherige Impfungen: First 2 covid vaccines had mild symptoms of fever, sore arm, fatigue.

VAERS 1964466

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NM
Alter: 35,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 18.12.2021
Beginn: 19.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Dyspnoea Heart rate increased

Symptomtext

Rapid heart beat (over 120 while resting according to smart watch), shortness of breath, dizziness from 19Dec-20Dec. Heart rate still up but breath/dizziness is no longer a concern.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Advil, 16 hours after vaccination
Allergien: Z-Pak
Vorherige Impfungen: -

VAERS 1964214

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

moderat

Staat: NC
Alter: 49,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Cough Dyspnoea

Symptomtext

Patient started to cough and had trouble breathing within 30 seconds after administration. Epi-Pen 0.3 was administered to left lateral leg with good response and 911 initiated

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Amlodipine, lamotrigine, levetiracetam, lisinopril-hydrochlorothiazide
Allergien: Iodinated contrast media, tree nuts, lidocaine, ondansetron, Sulfa, honey bees
Vorherige Impfungen: -

VAERS 2716956

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 22.11.2023
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Bursitis Dysmenorrhoea Heavy menstrual bleeding Neuralgia

Symptomtext

heavy painful periods 3 months after shot; heavy painful periods 3 months after shot; hip bursitis; nerve pain; hip pain; This spontaneous case was reported by a patient and describes the occurrence of DYSMENORRHOEA (heavy painful periods 3 months after shot), HEAVY MENSTRUAL BLEEDING (heavy painful periods 3 months after shot), BURSITIS (hip bursitis), NEURALGIA (nerve pain) and ARTHRALGIA (hip pain) in a 36-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 068h21a) for COVID-19 prophylaxis. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular use) 1 dosage form. On an unknown date, the patient experienced DYSMENORRHOEA (heavy painful periods 3 months after shot), HEAVY MENSTRUAL BLEEDING (heavy painful periods 3 months after shot), BURSITIS (hip bursitis), NEURALGIA (nerve pain) and ARTHRALGIA (hip pain). At the time of the report, DYSMENORRHOEA (heavy painful periods 3 months after shot), NEURALGIA (nerve pain) and ARTHRALGIA (hip pain) was resolving and HEAVY MENSTRUAL BLEEDING (heavy painful periods 3 months after shot) and BURSITIS (hip bursitis) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Intramuscular use) was unknown. Concomitant and specific treatment medications were not reported. Patient experienced heavy painful periods 3 months after shot. nerve pain and IT/hip pain. Patient needed physical therapy for almost 3 months It was unknown if the patient experienced any additional symptoms/events. Medication Details and reason for taking the medicine was reported as physical therapy, OTC pain pills, acupuncture. Lab data/results: Patient got hip bursitis as a result from all the nerve pain and was unable to walk for a couple months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2589321

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: FL
Alter: 73,0
Geschlecht: F
Eingang: 01.03.2023
Impfdatum: 28.02.2022
Beginn: 22.09.2022
Tage bis Beginn: 206,0
Dosis: 4
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Fatigue Oropharyngeal pain Pyrexia SARS-CoV-2 test positive

Symptomtext

This started with tiredness, sore throat slight fever lasting 4-5 days. Rapid test on the cruise ship. Positive.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Rapid test positive.
Aktuelle Erkrankungen: No
Vorgeschichte: Diabetes; Autoimmune disease of the liver
Andere Medikamente: NOVOLOG; LANTUS; azathioprine; PLAVIX; losartan; TRULICITY; vitamin D3; ALIGN; turmeric; vitamin B; FIBERCON; COLASE; coQ10; prednisone
Allergien: Sulfa
Vorherige Impfungen: Second Covid shot, extremely tired and slept for a couple of days after. 2/10/2021 Moderna

VAERS 2574216

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 02.02.2023
Impfdatum: 20.12.2021
Beginn: 03.01.2023
Tage bis Beginn: 379,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Mental status changes Pyrexia SARS-CoV-2 test positive

Symptomtext

01/03/23 presents to ED for "ams, fever". PMHx of "Cirrhosis, Cholangitis, Elevated LFT's, HLD and SDH/TBI"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: 01/03/23 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2567860

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: GA
Alter: 30,0
Geschlecht: M
Eingang: 25.01.2023
Impfdatum: 22.01.2022
Beginn: 05.09.2022
Tage bis Beginn: 226,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blepharospasm Blood test Muscle spasms Pain

Symptomtext

A couple of months after receiving the vaccine, I've been experiencing cramps in my skull area. I've been trying to reduce the pain by taking ADVIL or letting the pain subside on its own. I've also developed an eye twitch since then as well. The twitch developed in September while the skull pain developed over the recent weeks. I saw a specialist, but they stated these symptoms could be fixed through exercise. They didn't really do a thorough examination to diagnosis my symptoms and case.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Blood work & general assessment: date unknown
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Men's multivitamin; omega-3
Allergien: Mushrooms; lactose intolerant
Vorherige Impfungen: -

VAERS 2562263

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MO
Alter: 60,0
Geschlecht: F
Eingang: 18.01.2023
Impfdatum: 15.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: ja

Fatigue Nodule Paranasal sinus discomfort Rhinorrhoea SARS-CoV-2 test negative Sinusitis

Symptomtext

I had a Sinus infection with a running nose, sinus pressure. I also had a knot on my right arm. Also the day after the injection I was really fatigued for a couple hours. I seen a provider on 01/22/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 22JAN2022 COVID-19 negative
Aktuelle Erkrankungen: N/A
Vorgeschichte: Mild Asthma
Andere Medikamente: Imipramine; stool softener; ZYRTEC; SINGULAIR
Allergien: Aspirin; NOVOCAINE; morphine; DEMEROL; DARVON; tramadol; penicillin; cinnamon; raw pineapple; aloe vera
Vorherige Impfungen: When I was 1 years old, I got a DPT injection, 103 plus fever, screaming, my whole arm swallowed up.

VAERS 2546042

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MA
Alter: 55,0
Geschlecht: F
Eingang: 29.12.2022
Impfdatum: 22.09.2021
Beginn: 06.12.2022
Tage bis Beginn: 440,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Chills Fatigue Feeling abnormal Malaise Oropharyngeal pain SARS-CoV-2 test positive Sensory loss

Symptomtext

My COVID-19 symptoms started on 12/06/2022 I went to a work party at around 08:00PM, where I couldn't feel the drink that I was drinking. It felt weird. On 12/07/2022 I had a fatigue and a sore throat. By the evening my symptom's got worse along with the symptoms I got chills. I did a home COVID-19 test on 12/09/2022 which was positive. On 12/10/2022 I called my doctor's office on Saturday since it was a weekend the office was closed my phone line was transferred to a hotline. They told me to fill out a form which I did it online and said someone will get back to me within 24 hours. The PAXLOVID will be shipped within 1-2 business days since my symptoms already started and it was the 3rd day of my symptoms. The time frame for the PAXLOVID to work was within 5 days of my symptoms. I decided not to wait to the medication. I took TYLENOL for first couple of nights.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: 29DEC2022 COVID-19 test positive
Aktuelle Erkrankungen: None
Vorgeschichte: Obesity; Depression
Andere Medikamente: ZOLOFT; WELLBUTRIN
Allergien: None
Vorherige Impfungen: -

VAERS 2536668

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CT
Alter: 52,0
Geschlecht: F
Eingang: 19.12.2022
Impfdatum: 07.12.2021
Beginn: 04.12.2022
Tage bis Beginn: 362,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Insomnia Nasal congestion Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test negative Sinus congestion Skin swelling Streptococcus test negative Throat irritation Upper-airway cough syndrome

Symptomtext

On December 4 2022 I began to feel a little sinus congestion and a raw throat feeling, TYLENOL or ZYRTEC was not helping on Tuesday December 5 2022 my doctor had me come in for both a COVID-19 and Strep throat test. I used my own home remedies of elderberries and honey which I finished, I also took generic brand THERAFLU day/night combinations they did not help and symptoms got worse, my nose was very congested and I had postnasal drip with almost incontrollable coughing my left side more congested and puffy, I also took ADVIL cold and sinus this helped ever so slightly, I began MUCINEX nighttime, as of the reported date this being the first night I could sleep in my own bed. I still have sore throat.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: COVID-19 and Strep throat tests both negative.
Aktuelle Erkrankungen: None
Vorgeschichte: Allergies; cats environmental
Andere Medikamente: ZYRTEC; TYLENOL arthritis
Allergien: None
Vorherige Impfungen: -

VAERS 2475799

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: TX
Alter: 30,0
Geschlecht: M
Eingang: 11.10.2022
Impfdatum: 09.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Allergy test Discomfort Emotional distress Lip swelling Mechanical urticaria Pruritus Rash Skin test Urticaria Wheezing

Symptomtext

1/18/22: Started as mild itchiness, rash, and mild upper lip swelling. Resolved with one dose of Benadryl. 1/19/22: Itchiness worsened, generalized hives. 1/20/22: itchiness and hives persistent. Seen by PCP, I was itchy non-stop. She thought it was stress, gave me Xanax. No improvement. Went to dermatologist. Diagnosed with dermatographism. Started orapred, ranitidine, and Zyrtec. No improvement. Follow up a week after, instructed to continue allergy meds, Xolair was an option to consider. Feb 2022: seen by allergist, was instructed to stop all medications, started xyzal, hydroxyzine. Was told Xolair is for severe asthma, can use for chronic hives but doesn't think I need to. 2/6/2022: randomly started wheezing for the first time ever, no distress, Benadryl helped. 2/15/2022: Randomly started wheezing, audibly louder but no distress. Benadryl helped. Since May, I have been taking Xolair monthly, relieved symptoms but now starting to return. I am so uncomfortable and embarrassed in public.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: Allergy skin test
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Descovy
Allergien: Hydrocodeine
Vorherige Impfungen: -

VAERS 2433618

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MI
Alter: 60,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 19.03.2021
Beginn: 26.08.2022
Tage bis Beginn: 525,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Fatigue SARS-CoV-2 test positive

Symptomtext

08/26/22 presents to EC ED for "fatigue". PMHx of "HTN, protein malnutrition, infected pancreatic pseudocyst"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 08/26/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397631

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MD
Alter: 50,0
Geschlecht: M
Eingang: 30.07.2022
Impfdatum: 09.02.2022
Beginn: 28.07.2022
Tage bis Beginn: 169,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Dizziness Electrocardiogram abnormal Extrasystoles Laboratory test Ventricular extrasystoles Vertigo

Symptomtext

Dizziness / vertigo, new onset PVCs. In retrospect, may have been happening for several days and attributed to medication side-effects. Initially identified when a severe enough episode warranted taking vitals for communication with PCP. Noted skipped beats, confirmed with spouse and then utilized smart watch to obtain a Lead I ECG which showed frequent PVCs. Immediately engaged EMS, spent night at Hospital under observation. Tx included aspirin, potassium, meclizine and IV NS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Unknown labwork.
Aktuelle Erkrankungen: None
Vorgeschichte: Arthritis, nerve pain and related functional problems both lumbar and cervical.
Andere Medikamente: Dilaudid Bystolic Indomethecin Lidoderm Hyzaar Pataday Protonix Relistor Ritalin Concerta Valium Zyrtec Vit D
Allergien: Augmentin (poss)
Vorherige Impfungen: -

VAERS 2393888

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: -
Alter: 20,0
Geschlecht: F
Eingang: 27.07.2022
Impfdatum: 11.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Anxiety Lip swelling Stress Swelling of eyelid Urticaria

Symptomtext

On initial reaction on 1/20/2022 I had hives on my lower and upper back and chest, neck, face, bottom of feet, ankles, and thighs. My lips were swollen and my eyes just about swelled shut. Majority of the symptoms happened at night. During the day changes of temperature or stress/anxiety triggered them. During the day mostly hives on my neck, forearms, and hips would appear. This hives are no longer to that extent but I still to this day get hives every night and randomly during the day on the bottom of my feet, hips, butt, and upper back/neck. I took 1 tablet of Pepcid and Claritin after my prednisone dose which calmed the hives temporarily. Since going off of Pepcid and Claritin the hives are back in full force.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: After the booster I have had chronic hives ever since my first reaction after getting the booster.
Andere Medikamente: 20 mg D-Amphetamine twice a day
Allergien: None
Vorherige Impfungen: -

VAERS 2360941

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CT
Alter: 41,0
Geschlecht: M
Eingang: 07.07.2022
Impfdatum: 05.01.2022
Beginn: 12.06.2022
Tage bis Beginn: 158,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia COVID-19 Decreased appetite Diarrhoea Dry throat Fatigue Feeling hot Influenza Myalgia Oropharyngeal pain Productive cough Pyrexia SARS-CoV-2 test positive

Symptomtext

06/12/2022 I had early flu symptoms. I had a slight fever, felt tired and fatigued, my muscles and my joints ached. I took Tylenol thinking I was just tired and fatigued from traveling. It got better the following day. The symptoms rebounded and became much worse on 6/14/2022. I had a fever of 102.9, my eyes felt hot, had dry and sore throat with a cough that eventually progressed with phlegm. The pain in my muscles and joints became worse. I had loss of appetite. I had intermittent bouts of diarrhea. On 6/14/2022 in the evening, I took the COVID home antigen test, and it was positive. I had a telehealth appointment on 6/15/2022. I was prescribed Paxlovid, Medrol dose pack and recommended I use Vitamin D3, Vitamin C and Zinc. For fever control, I was instructed to alternate Ibuprofen and Tylenol. I started Paxlovid on 6/16/2022. I took it the full five days. I was sick until about 6/21/2022. I was still symptomatic, but I was better. I had intermittent cough, my diarrhea and fever were gone, the aches were gone. It was basically the cough and fatigue that was ongoing. On 6/21/2022 I had a COVID PCR test which was still positive. I started feeling complete resolution by 6/29/2022. I repeated a COVID PCR on 7/1/2022 that was negative. I have completely recovered now. I was out of the country from 6/4/2022 to 6/10/2022. My antigen test, on 6/10/2022, to leave the country was negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: COVID antigen tests, negative and positive COVID PCR tests, negative and positive
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes Type 2; Hypertension; Hyperlipidemia; Sinus Tachycardia; NASH
Andere Medikamente: Metformin; Diltiazem ER; Losartan; Atorvastatin; Cinnamon; Calcium with Vitamin D; Vitamin C; Fibercon; Fish oil; Multi Vitamin; Vitamin B Complex; Milk Thistle
Allergien: Lisinopril
Vorherige Impfungen: Moderna , 2nd dose. Bells Palsy

VAERS 2338973

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A (?)

mild

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 22.12.2021
Beginn: 27.06.2022
Tage bis Beginn: 187,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Arthritis Joint range of motion decreased Magnetic resonance imaging abnormal Periarthritis Product administered at inappropriate site X-ray abnormal

Symptomtext

Vaccine was given very high on the arm/shoulder and missed the deltoid. Pain in shoulder joint from the beginning and getting worse over the months, including reduced range of motion. MRI results indicated inflammation and adhesive capsulitis. Ongoing treatment with physical therapy and soon to schedule a cortisone shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Xray 05/06/2022) and MRI (05/29/2022)
Aktuelle Erkrankungen: none
Vorgeschichte: Migraine
Andere Medikamente: Imitrex for migranes, Calcium, Zinc, Magnesium, Potassium, Super B complex, Chlortrimeton, Vitamin D, Vitamin C, Women's Multivitamins.
Allergien: none
Vorherige Impfungen: -

VAERS 2332377

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 23.12.2021
Beginn: 08.06.2022
Tage bis Beginn: 167,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Exposure to SARS-CoV-2 Fatigue Malaise SARS-CoV-2 test positive Somnolence

Symptomtext

I started having symptoms two days before testing positive for COVID 19. I had really bad cough, felt really tired groggy, very under the weather. I took a home COVID 19 test for two days that showed negative. I knew I had come in contact with COVID 19 as both children were positive. On the third time testing it showed positive, I called my doctor who unfortunately was out of town. I did a virtual health visit with Urgent Care and was prescribed a Z-Pak. I tested negative on my thirteenth day of feeling unwell. I am now feeling much better just a dry cough is lingering.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Home COVID 19 Test
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, High Blood Pressure
Andere Medikamente: Blood Pressure Medication, Tylenol as needed, Claritin as needed,
Allergien: Hay Fever, Tree Pollen, Mold
Vorherige Impfungen: COVID 19 DOSE 1 Moderna Lot number 043B21A

VAERS 2315590

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NH
Alter: 40,0
Geschlecht: M
Eingang: 10.06.2022
Impfdatum: 08.01.2022
Beginn: 05.06.2022
Tage bis Beginn: 148,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 Cough Headache Oropharyngeal pain Pyrexia SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Five months after vaccination of dose 3 Moderna, on 6-4-2022, I started having a fever (did not check), headache and sore throat. The next day, it was just a sore throat. I called a doctor on 6-5-2022 who sent someone to test me for Covid. It was a positive result. I also made an appointment the see a doctor on 6-7-2022. They did not prescribe anything. They suggested cough drops. I started taking Strepsils (slurbiprofeno) 8.75mg OTC as needed. On 6-8, I developed a slight cough. I am feeling better but have a lingering cough. I am reporting my breakthrough case of Covid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: On 6-5-2022, one rapid Covid test from doctor's office-positive result.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2298707

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: CA
Alter: 45,0
Geschlecht: F
Eingang: 27.05.2022
Impfdatum: 04.03.2022
Beginn: 04.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthritis Decreased appetite Fatigue Hyperaesthesia teeth Localised infection Lymph node pain Lymphadenopathy Oral pain Osteoarthritis Toothache

Symptomtext

osteoarthritis pain increased, orthodontic pain (pressure from chewing, temperature sensitive), lymph node very swollen under infected arm (extremely painful, node was too swollen to wear a bra for a full week. node was similar in size to my breast- I am a D cup), lack of appetite. artritis and dental pain and fatigue started within 2 hours, node was noticed by 6 pm, swelling increased through the weekend, started to subside wednesday 3/9/22, but swelling was not gone for at least 4 days after. appetite still minimal. Allergist strongly recommended reporting reactions, she noted for future vaccinations for covid, I should be closely monitored

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: hEDS
Vorgeschichte: hEDS
Andere Medikamente: gabapentin 800mg and cyclobenzaprine 10mg 2-3x p/day, trazodone 50mg nightly
Allergien: tegaderm/ silver, yellow jacket venom, poison oak, codeine
Vorherige Impfungen: Moderna covid vaccine 8/3/21, and 9/7/21

VAERS 2285378

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 19.05.2022
Impfdatum: 21.02.2022
Beginn: 29.04.2022
Tage bis Beginn: 67,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Headache Nasopharyngitis

Symptomtext

I felt like I had bad cold on my way back home. I did a telehealth visit with my doctor Monday and was prescribed Paxlovid. I did not have a bad headache, it lasted for 3 days and I felt great after taking the medication.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Psoriatic arthritis
Andere Medikamente: Otezla; Wellbutrin; Celexa
Allergien: N/A
Vorherige Impfungen: -

VAERS 2271058

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: AZ
Alter: 63,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 25.02.2021
Beginn: 06.01.2022
Tage bis Beginn: 315,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Back pain Blood test Magnetic resonance imaging Spinal cord neoplasm Urine analysis X-ray

Symptomtext

01/06/2022 - Severe back paint 03/22/2022 - Diagnosed with spinal tumors (2)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: X-Ray, 2 MRI, Blood Tests & Urine Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Shoulder Pain
Andere Medikamente: Losartan Pravastatin Oxycodone
Allergien: None
Vorherige Impfungen: -

VAERS 2261980

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: VA
Alter: 51,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 02.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 4,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Blood creatine phosphokinase normal Blood creatinine increased Blood thyroid stimulating hormone normal C-reactive protein increased Fatigue Full blood count normal Glycosylated haemoglobin Joint stiffness Laboratory test normal Lipids normal Liver function test normal Musculoskeletal stiffness Myalgia Vitamin D White blood cell count increased

Symptomtext

Increased pain and stiffness in muscles and joints. Increased fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: vit d, ck,cbc, tsh, crp, liver function panel, hemoglobin A1C, lipid panel, chemistry panel all done 4/7/22 all normal except: CRP = 49, creatinine - 1.3, wbc - 14.4
Aktuelle Erkrankungen: none
Vorgeschichte: fibromyalgia, type 2 diabetes, hypertension, high cholesterol, gerd, ibs, insomnia, depression
Andere Medikamente: lyrica, cymbalta, metformin, losartan, seroquel, amlodipine, cyclobenaprine, atorvastatin, claritin, omeprazole, flonase, vitamin d
Allergien: codeine, ultram.
Vorherige Impfungen: -

VAERS 2259886

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CT
Alter: 41,0
Geschlecht: F
Eingang: 01.05.2022
Impfdatum: 29.12.2021
Beginn: 01.05.2022
Tage bis Beginn: 123,0
Dosis: 2
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal discomfort Cough Ear discomfort Laboratory test Oropharyngeal pain Rhinorrhoea Sneezing

Symptomtext

Cough, Sneezing, sore throat, runny nose, clogged ears. Upset stomach.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: Rapid Test 5/1/22.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2258415

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: IL
Alter: 33,0
Geschlecht: M
Eingang: 29.04.2022
Impfdatum: 11.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test Erythema Erythema multiforme Pain Pain in extremity Pruritus

Symptomtext

Three days after vaccination I went to see the doctor because I started itching and had redness all over but mainly in areas around joints, and it would not stop. He gave me a shot of cortisone. I was also prescribed a series of steroids as well as a scabies cream to apply to my skin. I got better 24 hours later. Then, on the highway, I went to the hospital emergency room because I was hurting all over, especially my feet. I was diagnosed with Erythema Multiforme. They told me that since I was still on prednisone, to increase fluids and rest. I am still experiencing these symptoms but they are much less acute.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Hospital performed some blood tests on 1-16-2022 but I don't know what they are.
Aktuelle Erkrankungen: Head cold 1 week prior to vaccination
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2254642

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: IL
Alter: 26,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 08.02.2022
Beginn: 11.04.2022
Tage bis Beginn: 62,0
Dosis: 3
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: unbekannt

Exposure during pregnancy Haematemesis Oropharyngeal pain Pyrexia

Symptomtext

Patient 12 weeks pregnant presents to ER with sore throat, fever (99.5) and vomiting of blood.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2243803

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NJ
Alter: 54,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 31.12.2021
Beginn: 03.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pain in extremity Secretion discharge

Symptomtext

I started getting a lot of built up mucus and pain in my leg. I'm still having the mucus at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Sarcoidosis
Andere Medikamente: Synthroid
Allergien: None
Vorherige Impfungen: -

VAERS 2243475

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: -
Alter: 82,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 05.03.2021
Beginn: 06.06.2021
Tage bis Beginn: 93,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Cough Diarrhoea SARS-CoV-2 test positive

Symptomtext

6/6/21 PMHx of skeletal tuberculosis, hypothyroidism, hyperlipidemia, "frequent pneumonias", presented to ER w/worsening cough and diarrhea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: 6/6/21 SARS-CoV-2 (COVID-19) by NAA, Micro Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2213673

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: -
Alter: 45,0
Geschlecht: M
Eingang: 03.04.2022
Impfdatum: 04.03.2022
Beginn: 11.03.2022
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Burning sensation Chills Decreased appetite Headache Neck pain Pain Photosensitivity reaction Sleep disorder

Symptomtext

44 year-old male with a past medical history most significant for OSA, chronic back pain, PTSD and traumatic brain injury. The patient received the Moderna vaccine on 1/4/22. He presented to the hospital on 3/11/22 and reported that he started having an intractable headache 4 to 5 days back. He explained his headache as burning, nonradiating 10/10 in intensity associated with neck pain. He also complained of photosensitivity but denied neck rigidity. Complaint chills, rigor and loss of appetite. The burning sensation kept him awake due to the pain, but after a few days it began to lessen in pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2213023

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CT
Alter: 59,0
Geschlecht: F
Eingang: 02.04.2022
Impfdatum: 23.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Feeling abnormal Impaired quality of life Pain Pain in extremity Sleep disorder Tinnitus

Symptomtext

This spontaneous case was reported by a consumer and describes the occurrence of PAIN (Achy), TINNITUS (Tinnitus), SLEEP DISORDER (Interferes with my relaxation and sleep), FEELING ABNORMAL (Feeling was unexplainable/ it was annoying) and IMPAIRED QUALITY OF LIFE (Affecting my quality of life) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Breast cancer (early stage) and Mastectomy (which was cured now) in 2021. Previously administered products included for COVID-19 vaccination: JANSSEN COVID-19 VACCINE (Batch Number JANSEN: 1805022) on 06-Mar-2021. Past adverse reactions to the above products included No adverse event with JANSSEN COVID-19 VACCINE. Concomitant products included LEVOTHYROXINE and LIOTHYRONINE SODIUM (CYTOMEL) for an unknown indication. On 23-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In December 2021, the patient experienced TINNITUS (Tinnitus), SLEEP DISORDER (Interferes with my relaxation and sleep), FEELING ABNORMAL (Feeling was unexplainable/ it was annoying) and IMPAIRED QUALITY OF LIFE (Affecting my quality of life). On 23-Dec-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced PAIN (Achy), FATIGUE (Tired) and PAIN IN EXTREMITY (Sore arm). The patient was treated with PARACETAMOL (TYLENOL [PARACETAMOL]) for Tinnitus, at an unspecified dose and frequency. At the time of the report, PAIN (Achy), FATIGUE (Tired) and PAIN IN EXTREMITY (Sore arm) was resolving and TINNITUS (Tinnitus), SLEEP DISORDER (Interferes with my relaxation and sleep), FEELING ABNORMAL (Feeling was unexplainable/ it was annoying) and IMPAIRED QUALITY OF LIFE (Affecting my quality of life) had not resolved. The patient had no known allergies. The patient never tested positive for COVID-19. The patient side effects from which she was struggling. 12 hours after the booster dose the patient got the usual effects like being tired, achy and had a sore arm. She went to sleep and rested then felt better the next day. Within the week after receiving the vaccine she developed tinnitus and which was nonstop since. She read tinnitus could be something linked to a COVID-19 vaccine. She noticed tinnitus when it was quiet. Tinnitus interferes with her relaxation and sleep. Tinnitus became constant and was still ongoing. The patient had not gone to see a doctor but as an appointment coming up. The feeling was unexplainable for the patient, and it was further mentioned that if she would know about those side effects, she would never take COVID-19 Vaccination. Other treatment included unspecified anti-inflammatories, acupuncture, and ear massages but nothing worked for her.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Breast cancer (early stage); Mastectomy (which was cured now).
Andere Medikamente: Levothyroxine; Cytomel
Allergien: -
Vorherige Impfungen: -

VAERS 2204047

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: VA
Alter: 57,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 24.03.2022
Beginn: 26.03.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Rash Rash pruritic

Symptomtext

rash that started 2 days after vaccine - initial spot on right foot, then behind her left knee, then multiple spots on left arm developed on 3/28; sites are itchy but not painful

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: none at this time; evaluation in office only
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: claritin
Allergien: penicillin
Vorherige Impfungen: -

VAERS 2200652

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 43,0
Geschlecht: F
Eingang: 26.03.2022
Impfdatum: 17.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

Arthralgia Immediate post-injection reaction Injection site pain Musculoskeletal stiffness Periarthritis X-ray

Symptomtext

The injection was painful immediately. Pain Got worse, deep ache soreness , proceeded into more widespread shoulder pain and stiffness , eventually became completely frozen shoulder

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: X-rays Physical Cortisone injection
Aktuelle Erkrankungen: No
Vorgeschichte: Thyroid
Andere Medikamente: Ibuprofen and Vicodin
Allergien: None
Vorherige Impfungen: -

VAERS 2197550

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NV
Alter: 59,0
Geschlecht: F
Eingang: 25.03.2022
Impfdatum: 24.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Cough Diarrhoea Malaise Nasopharyngitis Pyrexia

Symptomtext

10 HOURS AFTER I GOT THE BOOSTER SHOT, i WAS VERY ILL, A LOT SICKER THAN I WAS WHEN I HAD COVID. I EVEN TOOK A COVID TEST. THE FIRST 3 DAYS I HAD A FEVER 102 ,CHILLS. AFTER THAT I HAD DIARRHEA, FOR 2 DAYS. THEN FOR THE NEXT 7 DAYS I HAD THE WORST COLD EVER, THEN FOR 5 WEEEKS , I HAD A SERVERE COUGH, A BARK OF A COUGH, ON AND ON. TO THIS DAY I GET FITS A COUGHING.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: I WAS TOLD TO STAY AWAY FROM ER AND DOCTORS ITS JUST SIDE EFFECTS. SO NO TEST OR LABS WHAT WOULKD THAT TELL YOU. IM SO SURE A DOCTOR GIVE YOU A TEST FOR FLU?
Aktuelle Erkrankungen: NONE
Vorgeschichte: Some Liver damage
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: 59 YEARS OLD,04/03/21, PFIZER COVID-19 #ER8737

VAERS 2189941

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: ME
Alter: 22,0
Geschlecht: F
Eingang: 21.03.2022
Impfdatum: 06.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

C-reactive protein normal Eosinophil percentage Pharyngeal swelling Rash Rash pruritic Tongue pruritus

Symptomtext

11 days after booster dose, patient reported to PCP an itchy ash on her face, neck, head, back and axillary. Small red bumps. No new foods, soaps or bedding. Provided with hydroxyzine for relief of rash. Seen in office 3 days later and noted to have had some throat swelling along with the itching. Received systemic corticosteroids, famotidine and Zyrtec. referred to allergist. Rash persisted to dat. Allergist visit 3/14/22 - idiopathic versus autoimmune uticaria syndrome , possibly related to Moderna booster dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: SED Rate < 1 Eosinophil 2.3% C-reactive protein < 0.5
Aktuelle Erkrankungen: -
Vorgeschichte: ADHD, OCD, anxiety
Andere Medikamente: Vyvanse
Allergien: none
Vorherige Impfungen: -

VAERS 2183037

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: DC
Alter: 64,0
Geschlecht: F
Eingang: 16.03.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Fall Fatigue Oral herpes Vertigo

Symptomtext

fatigue lasted for 2 weeks, vertigo, dizziness, cold sore, fell oh 1/8/2022 and 1/15/22 fell at home

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: metformin, losatin, metoprolol
Allergien: -
Vorherige Impfungen: -

VAERS 2179864

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: VT
Alter: 17,0
Geschlecht: F
Eingang: 15.03.2022
Impfdatum: 09.02.2022
Beginn: 09.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Pain in extremity Product administered to patient of inappropriate age

Symptomtext

Patient received a moderna covid vaccine for the first dose of the series on 2/9/22. Patient should have received pfizer instead due to age. Pfizer covid vaccine given 03/09/2022 as second dose of series. department of health, patients parents and patient's PCP made aware of the error. Patient has now completed the covid vaccine series. No unexpected adverse events. Patient reported fatigue, sore arm and feeling run down after having Moderna vaccine. Symptoms lasted a day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No known
Vorgeschichte: -
Andere Medikamente: Loryna
Allergien: none
Vorherige Impfungen: -

VAERS 2178505

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 30,0
Geschlecht: M
Eingang: 14.03.2022
Impfdatum: 08.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test normal Pruritus Rash erythematous

Symptomtext

One week after I began with itchiness on my rear scalp, then my, neck, and upper torso. Through the weeks I would get random flares on all the body legs, arms stomach. Everywhere. Itchiness. In some I would have red rashes from scratching. Also faces flares on ears.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Blood order 2/22/2022- normal levels
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: N/a
Allergien: None known
Vorherige Impfungen: -

VAERS 2177223

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NY
Alter: 23,0
Geschlecht: M
Eingang: 13.03.2022
Impfdatum: 20.02.2022
Beginn: 03.03.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pruritus Urticaria

Symptomtext

Itching on various parts of the body occasionally throughout the day, including the palms, arms, legs, thighs, feet and back. Patient reported feeling small welts on the site of itchy skin when it occurs on the arms, back and thighs. This subsides after about an hour alongside the itching. Patient reported worsening of symptoms after taking showers.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2173344

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: CT
Alter: 53,0
Geschlecht: M
Eingang: 11.03.2022
Impfdatum: 07.01.2022
Beginn: 07.02.2022
Tage bis Beginn: 31,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Appendicitis Blood test Computerised tomogram abnormal Diarrhoea Feeding disorder Gastrointestinal disorder Intra-abdominal fluid collection Pain Surgery Vomiting

Symptomtext

On Feb 7, 2022 in the morning I had a lot of pain, GI issues that seemed like food poisoning- vomiting, diarrhea. I waited it out. Then called the doctor and they couldn't see me so I went to Urgent Care. They gave me anti-nausea but I couldn't eat and was in a lot of pain. So later that night I went to the ER they did testing. They determining I had appendicitis and then performed the surgery and gave me antibiotics because there was fluid in my abdomen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 2,0
Labordaten: Bloodwork, cat scan- appendicitis
Aktuelle Erkrankungen: No, I would have had a little cold or runny nose around the holiday. Nothing serious
Vorgeschichte: Hypothyroidism
Andere Medikamente: Multivitamin, Calcium, Flaxseed Oil, Estradiol, Medroxyprogesterone, Synthroid, Fexofenadine, Fluticasone Propionate
Allergien: No
Vorherige Impfungen: -

VAERS 2170985

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MA
Alter: 47,0
Geschlecht: M
Eingang: 10.03.2022
Impfdatum: 21.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Mechanical urticaria Pruritus Urticaria

Symptomtext

Acute urticaria; dermatographia; pruritis

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2170921

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 31,0
Geschlecht: M
Eingang: 10.03.2022
Impfdatum: 26.01.2022
Beginn: 09.02.2022
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Allergy test Anti-cyclic citrullinated peptide antibody Dizziness Glycosylated haemoglobin Hepatitis C antibody Impaired work ability Laboratory test Loss of personal independence in daily activities Mechanical urticaria Red blood cell sedimentation rate Reflex test Rheumatoid factor SARS-CoV-2 test Spinal X-ray Urticaria Vertigo Vitamin D

Symptomtext

I started getting severe hives from Feb 8-9th and when I consulted doctor they said its from vaccine stimulation. Its still continuing and I get hives which seems to come and go during different time of the day. Doctor called it as dermatographic urticaria. For the last few days I am also having dizzy/vertigo feeling and its affecting my normal./work life which I am worried about.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: VITAMIN D LEVEL ? Mar 1, 2022 ENVIRON ALLERGY PANEL Feb 24, 2022 MAJOR FOOD ALLERGY PANEL Feb 24, 2022 SEDIMENTATION RATE (ESR) Feb 24, 2022 RPR W REFLEX TITER Feb 24, 2022 CORONAVIRUS 2019 NAA(COVID-19 Feb 17, 2022 GENERAL HEALTH PANEL Jan 11, 2022 HEPATITIS C ANTIBODY RFLX HCV Jan 11, 2022 GLYCOHEMOGLOBIN A1C Jan 11, 2022 LIPID PROFILE Jan 11, 2022 LUPUS (SLE) PANEL Jan 11, 2022 CYCLIC CITRULLINATE PEPTIDE Jan 11, 2022 RHEUMATOID FACTOR (RA) QUANTI? , Jan 11, 2022 SEDIMENTATION RATE (ESR) Jan 11, 2022 XR THORACIC SPINE 2 VIEWS Jan 7, 2022
Aktuelle Erkrankungen: I had severe lower back pain during the first week of January. I never had it before.
Vorgeschichte: I dont have any.
Andere Medikamente: At the time or immediately after vaccination I dint take any medications.
Allergien: Not that I know about.
Vorherige Impfungen: -

VAERS 2166290

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NY
Alter: 46,0
Geschlecht: F
Eingang: 08.03.2022
Impfdatum: 16.02.2022
Beginn: 16.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dermatitis Erythema Perioral dermatitis Pruritus Rash Swelling face Urticaria

Symptomtext

I had rash/hives after the first and the second doses. This time (booster) is worse. Rash/Hives on lower body and belly. The next day My face was swollen with itchy and redness. I still get some weird rash/hives sometimes. I got severe dermatitis at midnight on Sunday and Monday. I had to go to a dermatologist and was told it is Perioral (periorificial) dermatitis. I have never had skin issues before the covid vaccine. My skin was healthy. I am 5'0 and 104#. It is not fair to get the same dose from someone big body frame.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: I need to do an allergy test.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Vitamin D and Vitamin C
Allergien: No
Vorherige Impfungen: -

VAERS 2162552

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CT
Alter: 31,0
Geschlecht: F
Eingang: 07.03.2022
Impfdatum: 12.01.2022
Beginn: 23.01.2022
Tage bis Beginn: 11,0
Dosis: UNK
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Fatigue Pruritus Urticaria

Symptomtext

Severe hives, fatigue, itch Symptoms are still present but relieved by a daily Zyrtec

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Never
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2158590

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MD
Alter: 34,0
Geschlecht: F
Eingang: 04.03.2022
Impfdatum: 13.01.2022
Beginn: 01.02.2022
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cyst removal Dermal cyst Discomfort Infection Inflammation Pruritus Urticaria

Symptomtext

Within 24 hours a sebaceous cyst on my back became inflamed and infected. Cyst was removed January 27 and was put on Augmentin for the infection. When starting augmentin I became consistently itchy at night. I spoke with my doc at a follow up appointment and she advised to stop taking the antibiotic if hives appeared. Hives appeared February 4 so I discontinued the antibiotics. The hives continued popping up after stopping the antibiotics, I followed up with my doc as I believe this has to do with the booster but she was not convinced. I'm still dealing with spontaneous hives multiple times a week. They typically start on my feet and travel up my legs but more recently they've started showing up on my chest and arms. There are days they are severely itchy and other days they just show up and are uncomfortable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Depression, Anxiety, obesity
Andere Medikamente: Trintellix 20mg, Klonopin .25mg, Omeprazole 40mg, Multivitamin, Probiotic, Vitamin C
Allergien: N/A
Vorherige Impfungen: -

VAERS 2151814

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 11.02.2022
Beginn: 13.02.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Deafness Ear discomfort Headache Rash Rash erythematous Tinnitus

Symptomtext

THE PATIENT RECEIVED MODERNA BOOSTER ON 2/11/22. 2 DAYS LATER, ON 2/13/22, THEY COMPLAINED OF A CLOGGING SENSATION OF THEIR LEFT EAR. IN ADDITION, THEY DEVELOPED A RED RASH THAT RADIATED FROM THE LEFT SIDE OF THEIR NECK TO THEIR MID CHEST REGION, HEADACHE & CHILLS. THEY DENIED PAIN, ITCHINESS OR BURNING SENSATION. THE PATIENT WAS SEEN BY THEIR PRIMARY CARE PROVIDER THAT THEN REFERRED THEM TO AN ENT. A COURSE OF STEROIDS & A MRI WERE PRESCRIBED. MRI NOT YET COMPLETED TO DATE. SIGNS & SYMPTOMS ARE REPORTED AS GETTING PROGRESSIVELY WORSE WITH HEARING LOSS & RINGING IN THE LEFT EAR IN ADDITION TO THE ORIGINALLY REPORTED CLOGGED FEELING.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: MRI SCHEDULED FOR 3/7/22
Aktuelle Erkrankungen: -
Vorgeschichte: MIGRAINES
Andere Medikamente: -
Allergien: CLINDAMYCIN
Vorherige Impfungen: -

VAERS 2131365

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 12.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Ageusia Arthralgia Bronchitis Cough Headache Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Severe headache, lost of taste, bronchitis reaction, joint pain, cough, and congestion.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Covid vaccine reaction.
Aktuelle Erkrankungen: N/A
Vorgeschichte: Asthma
Andere Medikamente: Ereo and multivitamins
Allergien: CT contrast dye and penicillin
Vorherige Impfungen: -

VAERS 2131183

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NY
Alter: 57,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 17.02.2022
Beginn: 18.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Nausea Pyrexia Urticaria Vomiting

Symptomtext

High fever, N&V x 8 hours , shaking chills, hives right upper arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: no
Aktuelle Erkrankungen: no
Vorgeschichte: HTN
Andere Medikamente: Amlodipine 5 mg PO QD
Allergien: Cipro, Thimerisol, PCN,
Vorherige Impfungen: -

VAERS 2131043

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NY
Alter: 66,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 04.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Fatigue

Symptomtext

The next day after the vaccination I had high fever, chills and extreme fatigue. It went on for a week, 100.3 Fever and I was taking Advil and rotating Tylenol. I did not see a doctor. I still have been experiencing fatigue but I was also just diagnosed with Cancer so i'm not sure if it has to do with cancer or vaccination.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Sjogren's syndrome
Vorgeschichte: Sjogren's syndrome
Andere Medikamente: Trazodone 50MG 1 a day, Hydroxychloroquine 200MG 1 a day.
Allergien: Sulfa and codeine.
Vorherige Impfungen: -

VAERS 2129420

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: RI
Alter: 22,0
Geschlecht: F
Eingang: 21.02.2022
Impfdatum: 28.12.2021
Beginn: 08.01.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Insomnia Mechanical urticaria Pruritus Rash Tinnitus

Symptomtext

11 days after booster participant started to get a rash all over body, itching, and ringing in ears. Participant can't sleep at due to the itching but improving. Symptom has been going on for a month and a half. Dermatographia has also been present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: Blood work to be done in a week.
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Prednisone Benadryl Claritin
Allergien: No
Vorherige Impfungen: -

VAERS 2128595

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: WI
Alter: 25,0
Geschlecht: F
Eingang: 20.02.2022
Impfdatum: 22.01.2022
Beginn: 01.02.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Joint swelling Pruritus Rash Sensitive skin Urticaria

Symptomtext

Rashes / hives after 9 days of getting booster shot Itchiness all over Ghost like rashes that disappear after a while Extremely sensitive and red skin Knee and elbow swelling one day after hives started and lasted for only a day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2123698

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NC
Alter: 29,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 31.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Injection site erythema Injection site pain Injection site swelling

Symptomtext

Site: Pain at injection site-Medium; Site: Redness at injection site-Medium; Site: Swelling at injection site-Medium.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2123225

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NY
Alter: 23,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 17.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Intermenstrual bleeding Menstruation irregular Pain

Symptomtext

When I recieved my first two shots I did not have any side effects. When I received my booster shot I had chills, body aches, etc. Then around 2 weeks (unknown of the exact date) later after receiving the booster I was experiencing irregular periods ( I have been on birth control for around 7 years and never had this happen). I was taking my birth control at the same time every night, I knew I did not have STI/STD?s because I was just tested. I called my OBGYN and abs was not sure why this was happening but said to wait another month and see if it continues. I waited until the next month after receiving my period and it is still going on. I received my period long before I was suppose to receive it and when I was suppose to receive it, I did not have it. I can?t think of any other reason this would be happening so my symptom is irregular periods and spotting.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Charlotte 24 Fe
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2123076

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: TX
Alter: 31,0
Geschlecht: F
Eingang: 18.02.2022
Impfdatum: 07.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Rash Urticaria

Symptomtext

Breaking out in hives everyday, dx with urticaria, no other known cause. Welts and rash all over body.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: -
Allergien: none
Vorherige Impfungen: same with 1st and 2nd dose of moderna

VAERS 2119276

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MA
Alter: 52,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 13.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Injection site pain Lymph node pain Lymphadenopathy Sleep disorder

Symptomtext

I developed painfully swollen lymph nodes in my left armpit. At first it was uncomfortable enough that I could not sleep on my left side and would wake up if I rolled over. This lasted about a week and a half. They have calmed down some, but the area is still tender now, over a month later. I also had typical vaccination related symptoms (fatigue, soreness at the injection site) but these seemed typical; however, this seemed more typical and do not concern me.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Low thyroid
Andere Medikamente: levothyroxine 75 mcg per day, armodafinil 75 mg per day, estradiol .025 patch (2x per week), progesterone 100 mg per day, vitamin D 1000 mg per day, "One a Day" women's formula multivitamin 1 per day
Allergien: Food allergy: all forms melon (watermelon, cantaloupe, honeydew)
Vorherige Impfungen: -

VAERS 2119084

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: IL
Alter: 38,0
Geschlecht: F
Eingang: 17.02.2022
Impfdatum: 21.01.2022
Beginn: 01.02.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Urticaria

Symptomtext

Hives began on 2/1/22. Appeared on extremities and head progressed to entire body over the next few days. Has continued since that date. Is controlled with antihistamines and topical ointments. If combinations of antihistamines are not taken hives reoccur quickly.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: psoriasis
Andere Medikamente: levothyroxine 50mcg daily loratidine 10mg BID
Allergien: bactrim azithromycin soy
Vorherige Impfungen: -

VAERS 2116733

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: KS
Alter: 55,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 28.01.2022
Beginn: 06.02.2022
Tage bis Beginn: 9,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Ear pain Oropharyngeal pain Pain

Symptomtext

I RECEIVED MY VACCINATION ON FRIDAY, JANUARY 28, 2022 BETWEEN 9:30 AND 9:40 AM. ON SUNDAY, FEBRUARY 6, 2022, AT ABOUT 3:30 PM, I DEVELOPED A BILATERAL SORE THROAT ORIGINATING IN MY LYMPH GLANDS AS WELL AS DOUBLE EARACHES. I SAW MY DOCTOR'S PA, AND SHE CHECKED EVERYTHING AND SAID SHE BELIEVES THE PAIN WAS CAUSED BY THE VACCINATION AND TOLD ME TO WAIT A FEW DAYS AND IT WOULD RESOLVE ON IT'S OWN, WHICH IT DID 1-2 DAYS LATER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: SCAB ON LEFT NASAL TURBINATE EAR ACHE AND BILATERAL SORE THROAT (NEAR THYROID GLANDS) DEVELOPED ON 02/06/2022
Vorgeschichte: SEVERE ALLERGIES ASTHMA LOW HORMONES ADHD HEARTBURN
Andere Medikamente: XOLAIR ADDERALL XR 30 MG IMIPRAMINE 25 MG ESTROGEN PROGESTERONE TESTOSTERONE SINGULAIR OMEPRAZOLE XYZAL FLONASE AZELASTINE NOSE SPRAY SPIRONOLACTONE TRELEGY TRAZADONE 25 MG MUPIROCIN OINTMENT (NOSE) GUIFINISEN VITAMIN D 2000 I.U. VITAMIN B
Allergien: GLUTEN
Vorherige Impfungen: SHINGRIX, AGE 53, I RECEIVED MY SHINGRIX SHOT ON 09/14/2019 AND WAS DIAGNOSED WITH SHINGLES ON 09/17/19

VAERS 2116408

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: MI
Alter: 51,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 05.02.2022
Beginn: 05.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site pain

Symptomtext

Site: Pain at Injection Site-Medium

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2110471

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NC
Alter: 41,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 26.12.2021
Beginn: 05.01.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Eye haemorrhage Fatigue Mechanical urticaria Urticaria

Symptomtext

Hives all over body, including eyes, face, neck, torso, legs, arms, palms of hands and soles of feet. Still have them as of today but symptoms are somewhat managed by antihistamines, diet, etc. Dermographia now present at random as well. Also fatigue, a blood vessel in my right eye burst (healed now), and general low energy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 3 doctors visits- first to Urgent care, one to PCP and one to Allergist
Aktuelle Erkrankungen: none
Vorgeschichte: autoimmune thyroiditis
Andere Medikamente: None
Allergien: Sulpha Drugs, Vicodin
Vorherige Impfungen: -

VAERS 2109454

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CT
Alter: 40,0
Geschlecht: F
Eingang: 12.02.2022
Impfdatum: 06.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Peripheral swelling Swelling Urticaria

Symptomtext

severe swelling under arm and on chest. Then on day 11 post vaccine, I broke out in hives. I've had terrible hives for the past 4 weeks and they are not yet gone away. I have been taking Zyrtec and will be going to an allergist this week

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2105470

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: VA
Alter: 40,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 26.01.2022
Beginn: 08.02.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Mechanical urticaria Pruritus Urticaria

Symptomtext

Extreme all over body itching with urticaria and dermagraphia started 14 days after I got my Moderna booster.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2102337

UNKNOWN MANUFACTURER · VACCINE NOT SPECIFIED (NO BRAND NAME) · Charge 068H21A

mild

Staat: MI
Alter: 35,0
Geschlecht: F
Eingang: 10.02.2022
Impfdatum: 10.02.2022
Beginn: 10.02.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Flushing Skin warm Urticaria

Symptomtext

Patient stated she went and received 2nd dose Moderna at 0920. She stayed for 30 minutes and they let her leave, as she was getting into car with the kids, she felt her face flush and hot, she saw hives on her face, neck and arms. Did not go back in but called us at 1700 to report the symptoms. She stated her symptoms resolved completely after about 2 hours by around 11am

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none reported
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: Bee sting kit and Penicillin (hives)
Vorherige Impfungen: -

VAERS 2095891

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: IL
Alter: 65,0
Geschlecht: F
Eingang: 08.02.2022
Impfdatum: 08.02.2022
Beginn: 08.02.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Pruritus Urticaria

Symptomtext

Pt. reported having itchiness on face and neck and reported hives @1259. Offered cetirizine and pt. refused. Called EMT to site and vitals taken - 189/120- left arm, 106-HR, 100% RA , BS-202 @ 1303. Offered diphenhydramine and pt. accepted. Provided oral diphenhydramine. Pt. requested ambulance. Once ambulance service arrived, pt. refused. Pt. left vaccination site with family via car.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: COPD, diabetes, asthma, HTN
Andere Medikamente: blood thinners, BP meds
Allergien: tape, IV contrast, hydrocodone, flu vaccine
Vorherige Impfungen: Flu vaccine

VAERS 2095489

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NH
Alter: 20,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 17.01.2022
Beginn: 07.02.2022
Tage bis Beginn: 21,0
Dosis: 3
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Mechanical urticaria Urticaria

Symptomtext

urticaria with dermatographism

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: na
Aktuelle Erkrankungen: none
Vorgeschichte: asthma
Andere Medikamente: none
Allergien: tree nuts
Vorherige Impfungen: -

VAERS 2095392

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: IN
Alter: 28,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: 05.02.2022
Beginn: 06.02.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Fatigue Headache Interchange of vaccine products Lymphadenopathy Pyrexia

Symptomtext

I got J&J shot first a year ago. This was my booster. Suffered fever, chills, fatigue, headaches, severe lymph node swelling under target arm. No treatment taken but rest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: I had similar reactions to the initial J&J vaccine at age 27 in summer of 2021.

VAERS 2091787

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MD
Alter: 56,0
Geschlecht: F
Eingang: 06.02.2022
Impfdatum: 28.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Fatigue Headache Malaise Pain Sleep disorder

Symptomtext

History: Covid-19 illness 02/2020, Long Covid symptoms started 03/2020. Long Covid symptoms recurred following initial 2-dose vaccination (2/23/21 & 3/23/21), subsided slightly, recurred again following dose 3 (8/27/21), had almost completely subsided prior to dose 4 (1/28/22). Symptoms since Dose 4: chronic fatigue, extreme post-exertional malaise, joint pain (mostly elbows & knees), severe body aches, headaches, disturbed sleep I can't find a specific Long Covid site to report this to.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Ulcerative colitis Depression Seasonal allergies LONG COVID
Andere Medikamente: Xeljanz Mesalamine (tablets & suppository) Prozac Xyzal Curamed Iron B-vitamin complex Magnesium
Allergien: None
Vorherige Impfungen: See note related to recent vaccine

VAERS 2087835

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MD
Alter: 18,0
Geschlecht: M
Eingang: 04.02.2022
Impfdatum: 03.01.2022
Beginn: 15.01.2022
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Blood test Mechanical urticaria Pruritus Rash Urticaria

Symptomtext

Extreme itching, rash, hives over torso, back, legs, arms and neck, made worse by scratching. Scratching results in raised markings (referred to as dermotographia by diagnosing doctor). Itching lasts about an hour., marks last longer. Symptoms started about 12 days after vaccination, and today, 32 days after vaccination, they are still present. They appear daily at different times and with varying degrees of severity. The itching sensation has been minimized by the use of Claritin and Benadryl, but the rashes continue to come and go.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: Dermatologist ran blood work, indicating no underlying infection.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Allergic to peanuts, tree nuts, fish and concentrated sesame. Had no exposure to these foods.
Vorherige Impfungen: -

VAERS 2087819

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: WA
Alter: 62,0
Geschlecht: F
Eingang: 04.02.2022
Impfdatum: 13.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Headache Incorrect dose administered Injection site pain

Symptomtext

Patient was to receive 0.25mL booster dose, instead received 0.5mL of Moderna COVID-19 vaccine. Sore arm for 4-5 days after injection and headache the day after.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: HTN; alcohol abuse; hyperglycemia; hyperlipidemia; anxiety; depression; osteopenia; Vitamin D deficiency
Andere Medikamente: Atorvastatin; Vitamin D2; Lisinopril; Alendronate
Allergien: PCN
Vorherige Impfungen: -

VAERS 2082299

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NC
Alter: 33,0
Geschlecht: F
Eingang: 02.02.2022
Impfdatum: 12.01.2022
Beginn: 15.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Pruritus Urticaria

Symptomtext

On the 15th I noticed a big red welt at my arm. Not at injection site. I had a couple on my back and one on my other arm. Monday morning, I had one on my foot that was really itchy. I figured it was a booster reaction. I contacted Primary Care and the provider prescribed topical steroid and Benadryl. The 23rd my head was very itchy. I thought my family had lice so you treated everyone for lice Sunday evening 01/23/2022 I contacted my Dermatologist. I saw a PA and I cannot remember the name but I was prescribed Zyrtec OTC twice a day for 2 weeks and then once a week for remaining 6 weeks for 2 months total. She also prescribed prednisone if it has not got better. The itching did get better but I am still covered in hives from head to toe.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: The PA with Cary Dermatology stated they would run tests after 2 month if they were still present.
Aktuelle Erkrankungen: No. We may have had Covid at time of booster from exposure but I had no symptoms and didn't get tested. When I had Covid in October 1oth Monday you did had monoclonal antibodies
Vorgeschichte: Hashimotos Hypothyroid
Andere Medikamente: Synthroid 25MCG daily Cingular 10MG 1xdaily Multivitamin 2000IU Vitamin D daily
Allergien: Leviquin
Vorherige Impfungen: -

VAERS 2079486

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: DE
Alter: 63,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 04.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 12,0
Dosis: UNK
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Diarrhoea Pyrexia

Symptomtext

Fever, chills, and diarhea...self-treated with Tylenol and plenty of fluids. Effects lasted for 2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Refer to medications section in Item #9.
Andere Medikamente: Implanted pacemaker (bradycardia), Olmasartan (high blood pressure), Atorvorastatin (high cholesterol), Jardiance (borderline diabetic), Eliquis (blood thinner), Metoprolol (tachacardia).
Allergien: Penicillin causes swelling and rash in legs, as of 18 yrs old result of double viral pneumonia - hospitalized for 12 days.
Vorherige Impfungen: -

VAERS 2079156

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: FL
Alter: 33,0
Geschlecht: F
Eingang: 01.02.2022
Impfdatum: 26.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Interchange of vaccine products Pruritus Swelling Urticaria

Symptomtext

Received Janssen on 04/10/2021 filed VAERS report, report ID -1654072 . With 1st dose started having serve reactions, that were controlled with injections. After booster shot, the symptoms restarted, including swelling, itching, redness (hives) all over entire body. Followed up with PCP, and Allergist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Xolair injections, multi-vitamin, OTC allergy medicine
Allergien: -
Vorherige Impfungen: see VAERS ID 1654072, from Janssen dose #1

VAERS 2076891

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: OH
Alter: 46,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 28.01.2022
Beginn: 31.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Pain in extremity Peripheral swelling Skin warm

Symptomtext

Patient called to say her arm was red, hot, sore and swollen to the "size of a baseball"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: --
Vorgeschichte: --
Andere Medikamente: unknown
Allergien: nkda
Vorherige Impfungen: similar reaction but didn't swell as much

VAERS 2075171

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 41,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 28.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Adverse reaction Arthralgia Chills Diarrhoea Malaise Pain in extremity

Symptomtext

This adverse effect report is filed for the Moderna COVID-19 booster vaccine. The patient had received the Pfizer-BioNTech COVID-19 vaccine for the first 2 doses. Symptoms: malaise (started on first day, persisted for 3 days), joint ache at the left knee - there is some pain when the patient puts pressure on the left leg (started on first day, persisted for 3 days), chills (started on first day, persisted for 2 days), diarrhoea (started on the night of the third day)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Nil
Aktuelle Erkrankungen: Nil
Vorgeschichte: Low testosterone levels
Andere Medikamente: Testogel Clomiphene
Allergien: Penicillin
Vorherige Impfungen: Malaise (for the first 2 doses - started on first day and persisted for 2 days), fever (for the second dose, one day)

VAERS 2075169

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 41,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 28.01.2022
Beginn: 28.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Chills Diarrhoea Malaise Pain in extremity

Symptomtext

This adverse events report is filed for the Moderna COVID-19 booster vaccine. The patient had taken the Pfizer-BioNTech COVID-19 vaccine for the first two shots. Symptoms - malaise (for 3 days), joint ache - left knee which aches when patient tried to put pressure on the leg (for 3 days), chills (first two days), and diarrhoea (started on the night of the third day)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Nil
Aktuelle Erkrankungen: Nil
Vorgeschichte: Low testosterone levels
Andere Medikamente: Testogel clomiphene
Allergien: Penicillin
Vorherige Impfungen: Malaise (up to 2 days for both the first and second doses), fever (for the first day of the 2nd dose)

VAERS 2074798

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 38,0
Geschlecht: F
Eingang: 30.01.2022
Impfdatum: 05.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dry skin Pain of skin Pruritus Rash

Symptomtext

Systemic: Allergic: Itch (specify: facial area, extremeties)-Medium, Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Additional Details: Patient developed rash, itching, dryness, and soreness on skin surrounding eyes 3 to 5 days after booster administration. Denies starting new diet/medication/skin products and any visual changes/disturbances. She has been taking OTC Claritin every day since symptom onset, which seems to help, but is concerned if symptoms will resolve on its own. Patient was advised to try OTC Benadryl and topical hydrocortisone for the next 2-3 days and to seek medical attention if symptoms are still not better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain of skin
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2074453

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: FL
Alter: 78,0
Geschlecht: F
Eingang: 29.01.2022
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Incorrect route of product administration Injection site pain

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Joint Pain-Medium, Additional Details: Pt states she thinks vaccinator hit a nerve. She is still experiencing pain at injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2070024

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: TX
Alter: 90,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Hypersomnia Injection site pain Interchange of vaccine products Sluggishness

Symptomtext

Patient received a Moderna covid-19 vaccine booster. Patient previously received the J&J one dose vaccine. Patient stated she was "knocked out" at 21:30 after having received the vaccine earlier in the day and was unable to "wake up" until the following day at 15:30. She stated that she remained sluggish the rest of the day. She reported feeling fine now and only had a slightly sore arm from the injection at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: taking Doxycycline Hyclate for Unknown bacterial infection 12/29/2021
Vorgeschichte: unknown
Andere Medikamente: Citalopram 10mg Letrozole 2.5mg
Allergien: cephalosporins penicillin
Vorherige Impfungen: -

VAERS 2068876

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: FL
Alter: 66,0
Geschlecht: F
Eingang: 27.01.2022
Impfdatum: 27.01.2022
Beginn: 27.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dizziness Flushing Headache

Symptomtext

PT REPORTED HEADACHE, LIGHT HEADEDNESS AND FLUSHED FEELING AFTER INJECTION.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: RECENT CHOLECYSTECTOMY ON 1/5/22
Vorgeschichte: CARPAL TUNNEL
Andere Medikamente: XANAX, CELEXA, FLEXERIL, GABAPENTIN, LEVOTHYROXINE, OMEPRAZOLE
Allergien: NO KNOWN ALLERGIES
Vorherige Impfungen: -

VAERS 2066023

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MO
Alter: 52,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 31.01.2021
Beginn: 01.01.2022
Tage bis Beginn: 335,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Breast pain Breast tenderness Mammogram normal Nephrolithiasis Sensitive skin Ultrasound abdomen Ultrasound biliary tract Ultrasound kidney Ultrasound liver

Symptomtext

Sharp pain under right breast that goes from front to back. Under side of right breast is tender and heightened sensitivity. Top of breast is fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast pain
Hospital-Tage: -
Labordaten: Mammogram 1/19/22 normal reading Ultrasound of gall bladder, liver, stomach and kidney 1/21/22 everything looked good, a 3mm kidney stone in right kidney
Aktuelle Erkrankungen: migraines
Vorgeschichte: migraines, fibromyalgia,
Andere Medikamente: Hydroxychloroquine, allopurinol, olmesartan, pantoprozolol, b12
Allergien: Tide detergent, pennicillin, cephalexin, sulfa drugs, triptan drugs, synthroid, clonazepam, injectable steroids,
Vorherige Impfungen: -

VAERS 2065196

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: AZ
Alter: 56,0
Geschlecht: F
Eingang: 26.01.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Rash

Symptomtext

Systemic: Allergic: Rash Generalized-Mild

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2062854

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 14.01.2022
Beginn: 24.01.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Headache Pruritus Pyrexia Rash Swelling Swelling face Urticaria

Symptomtext

Day after booster: fever, severe fatigue and throbbing headache. 10 days after booster: raised, itchy hives all over head/face/neck/pelvis and mild rash on arms/torso.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Appendicitis discovered on January 5, 2022, with appendix removed on January 6, 2022.
Vorgeschichte: Asthma, bronchitis, seasonal allergies
Andere Medikamente: Probiotic supplement
Allergien: Sulfa, Dairy
Vorherige Impfungen: 2nd dose of Moderna on 5/7/2021, severe fatigue/dizziness/headache.

VAERS 2062464

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MD
Alter: 27,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 14.01.2022
Beginn: 23.01.2022
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chest discomfort Urticaria

Symptomtext

Diffuse urticaria, chest tightness

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: N/a
Andere Medikamente: N/a
Allergien: NKDA, NKFA
Vorherige Impfungen: -

VAERS 2062350

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CT
Alter: 37,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 20.12.2021
Beginn: 24.01.2022
Tage bis Beginn: 35,0
Dosis: 3
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Headache Oropharyngeal pain Viral test

Symptomtext

Sore throat, Headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: PCR 01/24/2022
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2062175

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NY
Alter: 39,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Nausea Pyrexia Skin discolouration Vomiting

Symptomtext

Patient developed blue discoloration in her hands and feet 2 hour after receiving her Moderna 0.25mL booster. Approximately 24 hours after receiving she developed fever, nausea and vomiting. All adverse reactions completely resolved 48-72 hours after receiving her dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Allergy to amoxicillin
Vorherige Impfungen: -

VAERS 2058489

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NY
Alter: 34,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 26.05.2021
Beginn: 08.06.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: - / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Blister Fatigue Hypoacusis Oral mucosal eruption Pruritus Rash

Symptomtext

Near 1 wk following 1st dose, rash on arm with blistering, subsided within 1 mo. Near 1 wk following 2 dose rash on arm with blistering, has not subsided and visibly present at time of booster. Within 1 wk following booster, rash with blistering. Currently, rash with blistering both arms, mouth, nose. Tired ALL the time, joint pain, itchy all over, hearing impairment right ear. 2nd dose 6/22/21 Booster 1/13/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Advised bendryl from the pharmacist, prescribed nystatin ointment to treat suspected poison ivy by physician. Discontinued due to burning and inflamed rash. On 1/22/22 self use witch hazel on one small outbreak area - 1/24/22 witch hazel seems to be drying the blistering, but rash still present.
Aktuelle Erkrankungen: None.
Vorgeschichte: Gird.
Andere Medikamente: Seroquel; Zoloft; Acyclovir; Depo shot.
Allergien: Morphine.
Vorherige Impfungen: -

VAERS 2058484

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: OH
Alter: 90,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 20.01.2022
Beginn: 20.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Incorrect dose administered

Symptomtext

Patient was inadvertently given the full dose (0.5 ml) for the Moderna booster instead of standard 0.25 ml. Followed up with patient to see if immunocompromised in any way to qualify for full dose. Spoke with patient's daughter on 1/24/2022 (after leaving 3 messages for the family). Daughter confirmed mom was doing just fine with no adverse effects aside of a little fatigue like she had after first 2 doses. I would like to note here that patient is morbidly obese as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: not applicable
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes, hypertension, pacemaker
Andere Medikamente: Eliquis, Losartan, Januvia, Metformin, Metoprolol, Triamterene/HCTZ
Allergien: Cipro
Vorherige Impfungen: -

VAERS 2058069

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: WV
Alter: 42,0
Geschlecht: F
Eingang: 23.01.2022
Impfdatum: 08.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pruritus Rash erythematous Swelling Urticaria

Symptomtext

Red rash raised with hives, extremely itchy started Monday afternoon still happening Sunday. Taking Benadryl and Metrol Dosepak 4mg oral tablets since Thursday at 4 pm. Nothings helping it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Pictures of rash sent to Teladoc on Thursday @1100 am
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2054607

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: VA
Alter: 29,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 07.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Rash

Symptomtext

Tuesday: developed hive-like blanchable rash that was edematous which began on the back of my head and spread to my upper eye lids. Wednesday: same rash spread to inner thighs, groin, armpits. Thursday: rash became less edematous but much more wide spread. Still blanchable but appears to develop in areas where the skin endures trauma (scratching, rubbing against something rough, warm/hot water). Friday: rash remains the same as Thursday Tuesday and Wednesday I used Benadryl 50mg three times a day and switched to Zyrtec 10mg twice a day beginning Thursday and continue to use Zyrtec

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2054540

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21A

mild

Staat: NY
Alter: 60,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 03.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

Cold sweat Diarrhoea Dizziness Hyperhidrosis Malaise Pain

Symptomtext

TWO DAYS AFTER MY SHOT I GOT VIOLENTLY SICK WITH MASSIVE DIARRHEA, DIZZINESS, HOT/COLD SWEATS AND EXCRUTIATING PAIN AND ENDED UP IN THE ER

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: crab
Vorherige Impfungen: -

VAERS 2053930

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NY
Alter: 21,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Anxiety Odynophagia Pruritus

Symptomtext

Patient stated after receiving her booster shot around 15 to 20 mins after patient c/c of painful to swallow. Mild itchiness. No edema. Denies any rash, no edema of tongue, breathing difficulty or SOB, chest pain, dizziness or any other medical symptoms. Px was evaluated Vitals : BP: 101/66, RR 20 HR 97 Pulse ox (* at RA.) px was anxious, but alert, oriented by 3, no acute distress. lungs clear, HEENT: no edema, no rash. clear. heart : normal s1,s2, RRR. no murmur. EMS was called. evaluated patient was in stable condition and refused to go to ED. px went home with mother. in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Pulse Ox : 97 %
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Depression asthma
Andere Medikamente: currently taking the following Rx: Propranolol Hcl 40 mg, Dextroamphetamine-Amphetamine 10mg Ventolin
Allergien: None
Vorherige Impfungen: -

VAERS 2053248

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: -
Alter: 34,0
Geschlecht: F
Eingang: 21.01.2022
Impfdatum: 06.01.2022
Beginn: 17.01.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pruritus Sensitive skin Urticaria

Symptomtext

Hives, itching, sensitive skin, ~12 days after booster. Used topical anti-itch cream

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Celiac disease & lymphocytic colitis
Andere Medikamente: -
Allergien: Gluten- Celiac disease
Vorherige Impfungen: -

VAERS 2051083

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: KY
Alter: 29,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 13.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abnormal dreams Chills Hallucination Pyrexia

Symptomtext

Fever, Chills, Shivers, Hallucination/Vivid Dreams

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2048783

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MI
Alter: 23,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 26.12.2021
Beginn: 07.01.2022
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Pruritus Skin reaction Urticaria

Symptomtext

Started to feel intensely itchy the evening of the 17th as well as having the urticaria symptoms. Received a steroid shot on the 19th when I visited urgent care. PA prescribed medrol dosepack and hydroxyzine. Finished course of dosepack but still having same symptoms just not as intensely itchy as was initially. Skin is still highly reactive to any type of touch as of today, the 19th of January.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Larissa birth control
Allergien: None
Vorherige Impfungen: -

VAERS 2047738

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: VA
Alter: 23,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 13.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Heart rate decreased Immediate post-injection reaction

Symptomtext

Immediately following vaccination client developed dizziness and low pulse rate. Did not lose consciousness. Has had syncopal episodes in the past. Symptoms resolved after 3 minutes of rest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Vitals: Initial (12:05) 98/73, HR 65, 12:20 lying: 120/73, HR 65, 12:20 standing: 126/93, HR 81.
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2046159

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: OH
Alter: -
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 05.01.2022
Beginn: 01.01.2022
Tage bis Beginn: -
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Asthenia Cough Dysstasia Fatigue Muscular weakness Pain Rhinorrhoea SARS-CoV-2 test Somnolence

Symptomtext

Other pains going on; Slept more than 8 hours; Muscle weakness; Unable to stand for long periods of time; Runny nose; Feeling weak; Cough; Tired/muscles are tired/fatigue; This spontaneous case was reported by a consumer and describes the occurrence of PAIN (Other pains going on), SOMNOLENCE (Slept more than 8 hours), MUSCULAR WEAKNESS (Muscle weakness), DYSSTASIA (Unable to stand for long periods of time) and RHINORRHOEA (Runny nose) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 05-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In January 2022, the patient experienced PAIN (Other pains going on), SOMNOLENCE (Slept more than 8 hours), MUSCULAR WEAKNESS (Muscle weakness), DYSSTASIA (Unable to stand for long periods of time), RHINORRHOEA (Runny nose), ASTHENIA (Feeling weak), COUGH (Cough) and FATIGUE (Tired/muscles are tired/fatigue). The patient was treated with PARACETAMOL (TYLENOL EXTRA STRENGTH) for Adverse event, at an unspecified dose and frequency. At the time of the report, PAIN (Other pains going on), SOMNOLENCE (Slept more than 8 hours), MUSCULAR WEAKNESS (Muscle weakness), DYSSTASIA (Unable to stand for long periods of time), RHINORRHOEA (Runny nose), ASTHENIA (Feeling weak), COUGH (Cough) and FATIGUE (Tired/muscles are tired/fatigue) outcome was unknown. 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 medication was reported by the reporter. It was reported that, the patient had symptoms listed under Covid-19. Treatment included dirking liquids (orange and apple juice).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Test; Test Result: Negative ; Result Unstructured Data: Negative
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2046138

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MI
Alter: 19,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 06.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Erythema Eye swelling Immunisation reaction Joint swelling Lip swelling Pruritus Throat tightness Urticaria

Symptomtext

Swollen wrists; Sensation of throat closing/tightened throat; Itchiness all over the body; Hives covering entire body (raised welts and red dots in some places like hands and neck); immune reaction to the booster dose; red dots in various places on the body; swollen eyes and lips; swollen eyes and lips; This spontaneous case was reported by a consumer and describes the occurrence of ERYTHEMA (red dots in various places on the body), LIP SWELLING (swollen eyes and lips), EYE SWELLING (swollen eyes and lips), JOINT SWELLING (Swollen wrists) and THROAT TIGHTNESS (Sensation of throat closing/tightened throat) in a 19-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Previously administered products included for an unreported indication: JANSSEN COVID-19 VACCINE (J and J vaccine) on 07-Apr-2021. Concurrent medical conditions included Asthma since 01-Jan-2005, Hypersensitivity reaction, Hives, Latex allergy (reaction : hives and swollen lipes/eyes) since 06-Jan-2008 and Migraine (Migraines) since 01-Jan-2013. Concomitant products included FLUTICASONE PROPIONATE (FLOVENT) from January 2008 to an unknown date, MONTELUKAST SODIUM (SINGULAIR) from January 2018 to an unknown date, TOPIRAMATE from January 2014 to an unknown date, ETHINYLESTRADIOL, NORETHISTERONE (ALYACEN) from January 2020 to an unknown date and FOLIC ACID from 01-Jan-2020 to an unknown date for an unknown indication. On 06-Jan-2022 at 5:30 PM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Jan-2022, the patient experienced ERYTHEMA (red dots in various places on the body), LIP SWELLING (swollen eyes and lips), EYE SWELLING (swollen eyes and lips), THROAT TIGHTNESS (Sensation of throat closing/tightened throat), PRURITUS (Itchiness all over the body), URTICARIA (Hives covering entire body (raised welts and red dots in some places like hands and neck)) and IMMUNISATION REACTION (immune reaction to the booster dose). On 08-Jan-2022, the patient experienced JOINT SWELLING (Swollen wrists). The patient was treated with LEVOCETIRIZINE DIHYDROCHLORIDE (ALLEGRA [LEVOCETIRIZINE DIHYDROCHLORIDE]) ongoing from 07-Jan-2022 for Adverse event, at a dose of 180 milligram twice a day; PREDNISONE for Adverse event, at a dose of 20 milligram once a day and VITAMIN D NOS ongoing since an unknown date for Adverse event, at an unspecified dose and frequency. At the time of the report, ERYTHEMA (red dots in various places on the body), LIP SWELLING (swollen eyes and lips), EYE SWELLING (swollen eyes and lips), JOINT SWELLING (Swollen wrists), THROAT TIGHTNESS (Sensation of throat closing/tightened throat), PRURITUS (Itchiness all over the body), URTICARIA (Hives covering entire body (raised welts and red dots in some places like hands and neck)) and IMMUNISATION REACTION (immune reaction to the booster dose) had not resolved. The patient received the Moderna booster dose on 06-Jan-2022. Within 16 hours from taking the Moderna shot, the patient's entire body was covered in hives and throat felt tight but did not have any trouble breathing. The urgent care assessed it likely as a latex allergic reaction from the band aid that the pharmacy used after they administered the shot. The patient was prescribed prednisone but was asked not to use it until Sunday till 09-Jan-2022, as it would affect the effectiveness of the shot. Urgent care asked the patient to use Benadryl for the hives. The hives subsided during the day (itchy skin remained) but then started to return around 9 P.M. On 08-Jan-2022, the patient woke up to worse hives, including swollen eyes, lips, and wrists. The patient called the allergist who said that it was not a latex allergy but an immune reaction to the booster dose. The allergist asked the patient to take the Prednisone immediately and take Allegra 180 mg/twice daily. The hives had subsdided somewhat, but were still present for the patient every morning when the patient woke up. The allergist said that it could take a few weeks for the hives to disappear. Most recent FOLLOW-UP information incorporated above includes: On 15-Jan-2022: Follow received on 15-Jan-2022 contain significant information- Reporter added , Medical history of patient updated, Events added and patient demographics updated On 16-Jan-2022: Follow-up information received on 16-Jan-2022 contains non significant information

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Asthma; Hives; Hypersensitivity reaction; Latex allergy (reaction : hives and swollen lipes/eyes); Migraine (Migraines)
Vorgeschichte: -
Andere Medikamente: FLOVENT; SINGULAIR; TOPIRAMATE; ALYACEN; FOLIC ACID
Allergien: -
Vorherige Impfungen: -

VAERS 2045556

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: CA
Alter: 55,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Arthralgia Injection site pain Pain in extremity

Symptomtext

Site: Pain at Injection Site-Severe, Systemic: arm pain-Severe, Systemic: Joint Pain-Severe, Additional Details: Pt called stating she thinks the vaccine was given too high, cause her immense pain and she had to visit the urgent care. Arm is now in a sling and patient is taking tylenol #3 for the pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2045479

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: NY
Alter: 37,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 13.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Injection site pain Syringe issue Underdose

Symptomtext

Site: Pain at Injection Site-Mild, Additional Details: syringe was faulty , med dripped out of syringe, pt has to be given dose again after original dose dripped and patient did not get first dose "injection"---choose pain to continue but pt did not complain of pain (it was the only closest option so that we can proceed)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2045474

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 28,0
Geschlecht: M
Eingang: 19.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Injection site swelling

Symptomtext

Site: Swelling at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Medium

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2043674

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MO
Alter: 57,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 27.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Blood urine present Glucose tolerance impaired Laboratory test Nodule Pain Urge incontinence

Symptomtext

About 3 days after I received the vaccination I started to experience knots in the chest and breast area. I experienced body aching in my joints. The knots are on my right side of my body and they are still here. I also had blood in my urine this month on 01/14/2022 and I did get labs done on 01/18/2022 but no infection found. It feels like a UTI but not a UTI. I feel the sensation of having to go to the bathroom but does not have to go. I did as well have a culture done.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: lab results came back negative for a UTI.
Aktuelle Erkrankungen: None
Vorgeschichte: Used to be pre diabetic but not anymore
Andere Medikamente: Geriatric multivitamin with iron; calcium citrate; LEXAPRO generic; tramadol
Allergien: I am allergic to shellfish
Vorherige Impfungen: -

VAERS 2042817

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: VA
Alter: 19,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 12.01.2022
Beginn: 14.01.2022
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Urticaria

Symptomtext

hives over entire body

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 2042233

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: CA
Alter: 25,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 30.12.2021
Beginn: 10.01.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Injection site pain Pain Pruritus Skin irritation Skin reaction Skin swelling

Symptomtext

Remained asymptomatic after receiving moderna booster. I was only sore around injection site. Approximately 10 days after receiving the booster skin reactions and irritation occurred throughout my whole body. My skin felt uncontrollably itchy and after scratching that certain area my skin would flare up in raised red marks. The red marks/patches would vary in size. Some were more localized and other times they would flare up and cover a larger portion of my body. Sometimes the itchiness subsides quick but other times the itchiness is incontrollable and painful. There are no signs of a rash or bumps. I have been dealing with this skin reaction for a week now with no improvement. I have been taking Zyrtec daily and using topical hydrocortisone to stop the itching.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multi Vitamin, Vit D, Zinc
Allergien: None
Vorherige Impfungen: -

VAERS 2039886

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: TX
Alter: 58,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Epistaxis Injection site bruising Rash Skin discolouration

Symptomtext

Site: Bruising at Injection Site-Mild, Systemic: Allergic: Rash (specify: facial area, extremities)-Mild, Systemic: Nose bleed with black spots all over his body-Mild.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site bruising
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2039654

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: TX
Alter: 50,0
Geschlecht: M
Eingang: 17.01.2022
Impfdatum: 15.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site erythema Injection site pain Injection site pruritus Injection site swelling

Symptomtext

Swelling redness (2? diameter) sore to touch and localized itching at injection site

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: ALLERGIC RHINITIS DUE TO POLLEN (HAYFEVER)
Andere Medikamente: Zyrtec. Azelastine. Tadalafil. Testosterone.
Allergien: Sulfa group antibiotics
Vorherige Impfungen: -

VAERS 2038339

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 37,0
Geschlecht: F
Eingang: 16.01.2022
Impfdatum: 31.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Breast discomfort Burning sensation Cardiac discomfort Chest discomfort Discomfort Hypomenorrhoea Limb discomfort Menstruation irregular Ovarian disorder Pain Peripheral coldness Sensory disturbance

Symptomtext

Jan 1 around 1pm. Heart/ chest area: Pinching in & around my heart, behind sternum, upper left area, and in left arm pit. around 1pm: At the same time, I noticed a strong sensation in what I believe were my ovaries. It seemed like they were going through their own version of early labor contractions. It felt like something was trying to get out, or be pushed out. These ovarian contractions were slightly uncomfortable, but still strange. I do not usually notice when I ovulate, and when I have noticed, it's felt very light. I've given birth twice. It reminded me of early-mid labor contractions Jan 2 - 10: Left arm and leg sensations. I started noticing a new sensation in these limbs.The new sensation felt somewhat cold. It was not painful, but would catch my attention. It reminded me of how I remember feeling before pins and needles set in. This sensation increased over the days in intensity and how often it would show up and last. I noticed it more when I would sit upright in a chair and my legs would make about a 90 degree angle with my torso. I also noticed it increasingly when I'd stand up or walk around. The only time I never felt it was if I was laying down flat on my front or back, and not limbs were bent. Jan 9: The sensation started creeping up my legs further to my hips. Jan 10 & 11: The sensation also went to my lower and mid back a few times throughout the day. On Jan 11, I remember my legs actually feeling like they were starting to catch fire. I have yet to feel like my body is catching fire again. Jan 7: My period arrived 1 week early. Very light for 2 days (usually, the first day is the only light day, and the second day is the heaviest day). Jan 15: My left breast has felt uncomfortable. The uncomfortable feeling starts in the under side of my arm. I noticed in the morning when getting dressed. At one point today it was throbbing for about 20 minutes. It looks normal in color and shape, and I do not feel any lumps. Yet it still feels uncomfortable and throbs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: My health care provider ordered blood tests, which have not been conducted yet. They also referred me to a neurologist, who I will follow up with.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Zoloft, prenatal multivitamins, fish oil, vitamin D
Allergien: Penicillin, sulfa, sensitivity to milk
Vorherige Impfungen: -

VAERS 2038101

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MI
Alter: 19,0
Geschlecht: F
Eingang: 15.01.2022
Impfdatum: 06.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Eye swelling Interchange of vaccine products Joint swelling Lip swelling Pruritus Skin swelling Throat tightness Urticaria

Symptomtext

Received J&J vaccine on 4/7/21 and received the Moderna booster on 1/6/22. Within 16 hours from taking the Moderna shot, my entire body was covered in hives (raised welts, red skin, itchiness all over body, with red dots in various places on my body) and my throat felt tight but I didn't have any trouble breathing. My lips and eyes were swollen. I went to urgent care on 1/7/22 and they said that I likely had a latex allergic reaction from the bandaid that the pharmacy used after they administered the shot. They prescribed prednasone but said not to use it until Sunday, 1/9/22, as it would affect the effectiveness of the shot. Urgent care said to use benadryl for the hives. The hives subsided during the day (itchy skin remained) but then started to return around 9 pm. On Saturday, 1/8/22, I woke up to worse hives, including swollen eyes, lips, and wrists. The raised welts were all over my body with red dots in some places (hands and neck). I called my allergist who said it was not a latex allergy but an immune reaction to the booster. He said to take the Prednasone immediately and take Allegra 180 mg/twice daily. The hives have subsdided somewhat, but they are still there every morning when I wake up. I'm currently taking Allegra 180 mg/twice daily and Vitamin D. The allergist said that it could take a few weeks for the hives to disappear.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: No lab work was done at urgent care
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma Frequent Migraines
Andere Medikamente: Flovent 100: 1 puff daily Singulair 10 mg: 1 tablet daily Topiramate 100 mg; 1 tablet daily Alyacen 1/35; 1 tablet daily ProAir inhaler; 2 puffs as needed Folic Acid 1 mg: 1 tablet per day Imitrex 50 mg: 1 tablet as needed
Allergien: Latex
Vorherige Impfungen: -

VAERS 2037443

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge #068H21A

mild

Staat: DC
Alter: 46,0
Geschlecht: F
Eingang: 15.01.2022
Impfdatum: 12.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Eye pain Glossodynia Headache Pain Pain in extremity Peripheral swelling Swollen tongue

Symptomtext

1. Huge swelling and pain under arm of injection, started about 12 hours after vaccination 2. Swelling and pain under tongue on left side, started about 24 hours after vaccination 3. Throbbing pain in left eye, started about 12 hours after vaccination 4. Headache, started about 6 hours after vaccination 5. Body aches, started after about 4 hours after vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Eye pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D
Allergien: None
Vorherige Impfungen: Pfizer BioNTech

VAERS 2222767

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 13.01.2022
Impfdatum: 12.01.2022
Beginn: 12.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cold sweat Injection site hypoaesthesia Injection site pain

Symptomtext

injection site pain/numbness, clammy

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site hypoaesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2032475

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21A

mild

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Injection site erythema Injection site pain Injection site pruritus

Symptomtext

Patient received vaccine and a couple hours later her arm site became really red and itchy and tender to touch and it is about 2 inches below injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2025733

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: IN
Alter: 69,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 04.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Injection site pruritus Injection site rash Pain in extremity

Symptomtext

Sore arm, then itchy rash at injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lisinopril\HCTZ 10-12.5mg, Women's Daily Multivitamin, Calcium 1200 plus Vitamin D
Allergien: None
Vorherige Impfungen: -

VAERS 2025326

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 32,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 07.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Dizziness Hyperhidrosis Injection site erythema Injection site induration Injection site mass Injection site pain Injection site swelling Injection site warmth Lethargy Pain Pyrexia

Symptomtext

Injection site developed a 3 inch circular area of redness, swelling, was extremely hot and painful to the touch. Developed into hard mass. Dizziness the morning after the vaccine and throughout the day. Fever x3 days, body aches, lethargy, chills, profuse sweating

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Zofran
Vorherige Impfungen: -

VAERS 2025076

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NH
Alter: 66,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 08.01.2022
Beginn: 10.01.2022
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Erythema Mass Pain Skin warm

Symptomtext

Lump appeared on arm the size of a golf ball. (red and warm to touch). Chills, achy feeling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: Gabapentin, Doxycycline, Erythromycin.
Vorherige Impfungen: -

VAERS 2024711

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NC
Alter: 41,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 05.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Feeling abnormal Pain

Symptomtext

I began to experience fatigue, body aches and brain fog the day following the vaccination. I treated with rest and fluids. All symptoms resolved within 48 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2021369

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Fatigue Injection site discolouration Injection site nodule Injection site swelling Lymph node pain Pain

Symptomtext

After receiving the Moderna booster, I had chills for several hours on the day of injection. During the next 5 days I had a swollen and discolored hard knot at my injection site, sore lymph nodes near my arm pit on the injection arm, body aches, and fatigue. My symptoms lasted 6 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: N/a
Vorgeschichte: Spinal Muscular Atrophy
Andere Medikamente: Loryna, Spinraza
Allergien: Dairy
Vorherige Impfungen: Sore arm and swelling at injection site

VAERS 2021341

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: GA
Alter: 32,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 04.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cellulitis Erythema Feeling hot Induration Inflammation Pruritus

Symptomtext

Cellulitis - red, radiating heat, hard, inflamed, itchy deltoid; spread throughout entire upper arm, spread distal to forearm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, environmental allergies
Andere Medikamente: Zyrtec, below ogestrel, amlodipine, albuterol, Symbicort
Allergien: Cashews, pistachios, pineapple
Vorherige Impfungen: -

VAERS 2021236

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NY
Alter: 32,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 07.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Chills Fatigue Headache

Symptomtext

Headache, fatigue, chills - onset 12hr after vaccination - lasted for 12hr (resolved ~24hr from vaccination).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: NKDA
Vorherige Impfungen: 2nd dose Moderna COVID-19 vaccine. Received 2/3/21. Adverse Effects: headache, fatigue, chills.

VAERS 2021229

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: IL
Alter: 26,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 27.12.2021
Beginn: 09.01.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Mechanical urticaria Pruritus Urticaria

Symptomtext

Diagnosed with dermatographia after experiencing itching and hives.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: APRI birth control
Allergien: n/a
Vorherige Impfungen: -

VAERS 2020663

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MA
Alter: 31,0
Geschlecht: M
Eingang: 10.01.2022
Impfdatum: 21.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Mechanical urticaria Pruritus Urticaria

Symptomtext

Severe generalized hives, itching, and dermatographia occurring ~10 days post injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2019292

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: VA
Alter: 30,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 23.12.2021
Beginn: 05.01.2022
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Mechanical urticaria Urticaria

Symptomtext

Full-body hives accompanied by dermatagraphia. Improved but not definitively treated with Benadryl; 5-day course of prednisone beginning 8 January 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Kyleena
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 2018344

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: FL
Alter: 37,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 07.01.2022
Beginn: 08.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Abdominal pain lower Arthralgia Back pain Dysphagia Neck pain Pain in extremity

Symptomtext

Difficulty swallowing, pain in the left neck, left shoulder, left hand, left lower quadrant, across lower back and left knee

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain lower
Hospital-Tage: -
Labordaten: Non
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: None
Allergien: Sulfa
Vorherige Impfungen: Moderna

VAERS 2017493

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: OH
Alter: 36,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 06.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Axillary pain Fatigue Injection site erythema Injection site pain Lymphadenopathy Pain

Symptomtext

Pain and redness near injection site and Pain and swelling in left armpit. Overall fatigue and body aches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Axillary pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Cold 1 week prior
Vorgeschichte: Hypoparathyroidism, adhd, and depression
Andere Medikamente: Levothyroxine and bupropion
Allergien: None
Vorherige Impfungen: -

VAERS 2014952

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MN
Alter: 18,0
Geschlecht: M
Eingang: 07.01.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Rash papular Rash pruritic

Symptomtext

Rash raised and itchy.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash papular
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2014665

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 79,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 23.12.2021
Beginn: 24.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Burning sensation Injection site erythema Injection site swelling Injection site warmth Pain Pruritus Throat tightness

Symptomtext

On 12/24 Throat constriction and both arms itched and burned. On 12/28 Injection site swollen, hot to touch and very red. Had body aches that lasted through 12/31. Went to Urgent care on 12/30 but the doctor refused to give me a copy of the visit. He evidently didn't want to deal with it. Vaers also has an adverse reaction I had to first shot on02/28/2021. E-Report Number: 334192.Date of report 03/04/2021. Needless to say, I won't be getting any more shots.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None. The doctor didn't even look at my arm.
Aktuelle Erkrankungen: UTI
Vorgeschichte: None
Andere Medikamente: None at the time recorded.
Allergien: No
Vorherige Impfungen: Moderna

VAERS 2013929

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: TX
Alter: 46,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 05.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Groin pain Muscle spasms

Symptomtext

On 1/6/22 I started having period style cramps and cramping in the groin area. I had a hysterectomy 6 yrs ago and have been post menopausal for over 7 yrs. Advil helps but the pain in the groin area has not subsided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Groin pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Estradiol patch .5; omperozole 40mg; levothyroxine 50mcg
Allergien: None
Vorherige Impfungen: -

VAERS 2008816

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: MD
Alter: 39,0
Geschlecht: F
Eingang: 06.01.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Nausea Neuralgia Pain Pain in extremity

Symptomtext

Nausea, extreme nerve pain in arm shoulder and down the left side of my body.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: POTS, IBS, chronic back pain, migraines
Andere Medikamente: Wellbutrin, dycylomin, ibuprofen
Allergien: Penicillin bees
Vorherige Impfungen: -

VAERS 2002360

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CT
Alter: 34,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 02.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Vaccination site discomfort Vaccination site rash Vaccination site reaction Vaccination site swelling Vaccination site warmth

Symptomtext

I woke up the following morning with a swollen, hot, red rash below the vaccination site. This has continued to grow, is uncomfortable and looks identical to images of ?Covid arm?.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vaccination site rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Lorazepam, adderall, Prozac, seasonique, labetelol
Allergien: Bactrim
Vorherige Impfungen: -

VAERS 2002160

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 04.01.2022
Impfdatum: 30.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Feeling abnormal

Symptomtext

Patient stated he has been very tired and run down ever since he got the shot. He asked if that was normal. I said usually people only feel it for 1 to 2 days but if it's not getting better he should follow up with his Dr.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: got cough medicine prescribed 10 days prior
Vorgeschichte: gout, afib, diabetes
Andere Medikamente: metoprolol, atorvastatin, tamsulosin, sildenafil, metformin, lisinopril, potassium, bumetanide, warfarin, benzonatate prescribed 10 days prior
Allergien: none
Vorherige Impfungen: -

VAERS 2002110

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: OH
Alter: 48,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 22.12.2021
Beginn: 01.01.2022
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: ja Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood pressure increased Dermatologic examination abnormal Dizziness Fatigue Nausea Pruritus Rash erythematous Rash papular Rash pruritic Sleep disorder Throat tightness Urticaria

Symptomtext

Day 2 (Dec 23) woke up at 5 a,m, feeling nauseous, fatigued, light headed; symptoms lasted approximately 10 hours. By 3 pm I felt completely normal. Day 11 (January 1, 2022) woke up at 4 am with itchy scalp and hives covering the back of my head, back of neck and back of ears. As the day wore on hives appeared on front of neck, chest, legs, and feet. At 2 pm the hives continued to get worse. By 10 pm hives were breaking out all over back Day 12 (January 2, 2022) woke up at 4 am with hives on thighs, back, torso, front and back, shoulders and breasts. Hives were extremely itchy, red, raised. At 7 a.m. began to feel tightness in throat which continued for several more hours. at 10 a.m. arrived at the urgent care clinic where I was seen at approximately 10:30 a.m. saw dermatologist the next day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Blood pressure was taken and registered 150/110 (compared to my normally low blood pressure of 110/80) Observed by physician's assistant who told me I had hives and prescribed prednisone and Benedryl Tested at derm office who upped the dose of prednisone.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2000296

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: OH
Alter: 43,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Diarrhoea Dizziness Fatigue Lymphadenopathy Pain SARS-CoV-2 test negative Vomiting

Symptomtext

Dizzy,extreme tiredness,diarrhea, vomiting, body aches, lymph nodes in right under arm swollen (and still after four days) all symptoms lasted approximately 36 hrs except the swelling

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: At home rapid covid test with negative results
Aktuelle Erkrankungen: Typical sinus drainage and a bit of a stuffy nose
Vorgeschichte: Acid reflux, seasonal allergies
Andere Medikamente: Omeprazol Cetrizine
Allergien: -
Vorherige Impfungen: Same as above but no swelling of lymph nodes. Age 42 Vax date of 5/15/21. Moderna

VAERS 1999802

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: OH
Alter: 77,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SC / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Pruritus Urticaria

Symptomtext

Intense itching in my arms, lower back. Then I noticed little welts on my right arm. I also had some larger welts on my left thigh at the location of a skin graft, anterior location.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Heart failure and Chronic kidney disease.
Vorgeschichte: Anemia, depression.
Andere Medikamente: Elliquis, Diltiazem, Folic Acid, Atorvastatin Calcium , Metoprolol, Propalenone, Pioglitazone, Sertraline, Vitamin B-12, Albuterol. Lantus & Novolog insulin.
Allergien: None
Vorherige Impfungen: -

VAERS 1999748

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: TX
Alter: 45,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 28.12.2021
Beginn: 02.01.2022
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Cough Influenza virus test Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test

Symptomtext

pt w/complaint of sore throat, cough, runny nose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Oropharyngeal pain
Hospital-Tage: -
Labordaten: flu/sars testing
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1999276

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 47,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 23.12.2021
Beginn: 26.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chills Headache Hyperhidrosis Pain Pyrexia

Symptomtext

Patient reported severe body aches, chills, sweats and fever (continues to go higher since 12/26/2021). Currently taking Tylenol. Patient also having severe headaches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 1997920

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: SC
Alter: 27,0
Geschlecht: M
Eingang: 02.01.2022
Impfdatum: 20.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Fatigue Mechanical urticaria Rash Urticaria

Symptomtext

Chronic Spontaneous Urticaria (hives) and Dermatographia Large rashes covering both thighs, and bumps in random areas on palms, soles of feet, arms, chest, back, and lower legs. Treatment with antihistamines (diphenhydramine and loratadine taken at separate times) both are effective at reducing symptoms. Patient was also tired for day following vaccination

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Headache, Circular rash

VAERS 1997567

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: DC
Alter: 30,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 19.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Urticaria

Symptomtext

Full body hives

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Vitamin D, probiotics, fiber supplements, St. John?s Wort, Cranberry pills
Allergien: -
Vorherige Impfungen: -

VAERS 1997225

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: DC
Alter: 26,0
Geschlecht: F
Eingang: 01.01.2022
Impfdatum: 20.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Dermatitis Erythema Pruritus Skin swelling

Symptomtext

I started getting an unbearable itching sensation on various parts of my body approximately 8 days after my booster shot. If scratched, it would turn red, swell up (demotographia), and stay red and inflamed for aboout an hour after I leave it alone. I've been taking allegra every day to attempt to keep it under control but it only does so much. The itching and redness has spread now to my entire body including my hands and face.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: B-12 supplements
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1995992

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: TX
Alter: 19,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 29.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness Hyperhidrosis Nausea

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Flushed / Sweating-Severe, Additional Details: Patient experienced dizziness, light-headedness, profuse sweating, urge to vomit within 10 minutes of getting Moderna 0.25ml booster dose

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1995954

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: OH
Alter: 22,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Back pain

Symptomtext

The mother called stating patient had severe joint and back pain.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None currently
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: None known
Vorherige Impfungen: -

VAERS 1995934

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MI
Alter: 47,0
Geschlecht: M
Eingang: 31.12.2021
Impfdatum: 30.12.2021
Beginn: 31.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Chills Fatigue Headache Nausea Oropharyngeal pain

Symptomtext

Headache, nausea, chills, sore throat, fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Flonase, zertec
Allergien: None
Vorherige Impfungen: -

VAERS 1993256

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: IL
Alter: 28,0
Geschlecht: M
Eingang: 30.12.2021
Impfdatum: 27.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Testicular pain Testis discomfort

Symptomtext

I received booster on 12/27 on my left arm. On the morning of 29th I felt strong discomfort in my left testicle, but no swelling. Pain continued all day 29th and today 30th. It is only the left testicle and is painful to the touch. Last night I placed an ice pack on it.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Testicular pain
Hospital-Tage: -
Labordaten: Have not gone to the doctor yet.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1988856

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MO
Alter: 24,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 26.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Fatigue Headache Parosmia Throat clearing Throat irritation

Symptomtext

12/27: headache, slight tiredness 12/29: post workout(cardio)?- not abnormal in daily/weekly routine for workout?- 0500 smell of nickels/metallic smell. 0600?tickle in throat, constant need to clear throat, lungs CTA but chest feels like there is congestion and unable to clear throat or cough anything up. Metallic smell dissipated to barely noticeable by 1000.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Food poisoning- 12/21/2021? vomiting x5, diarrhea x4. Resolved mostly by mid afternoon. Diarrhea continued 12/22/2021 x1
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin, Keflex
Vorherige Impfungen: 11/29/2021: first dose Moderna (lot: 12H21B). Received at 11am on 11/28. At 0600 on 11/29? extreme tiredness, unable to stay awa

VAERS 1988802

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: PA
Alter: 43,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 27.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Blood test normal Heart rate increased Pyrexia SARS-CoV-2 test Urine analysis normal

Symptomtext

I spiked a fever of 105 degrees F and had a heart rate of over 180 bpm. After consultation with the Health Nurse Line, my boyfriend was told to take me immediately to the emergency room for treatment. Upon arrival, I was taken back as a "trauma cardiac event" and treated by the trauma team. They determined that the only thing that was different that could have caused this severe of an event was the fact I had had the Moderna COVID-19 booster shot about 24 hours prior.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: All routine blood and UA were normal. The COVID-19 PCR swab was still pending upon discharge from the hospital.
Aktuelle Erkrankungen: -
Vorgeschichte: Fibromyalgia Mitral Valve & Tricuspid Valve Prolapse Serotonin Syndrome Irritable Bowel Syndrome GERD/Hiatal hernia Iron Deficiency Anemia & Vitamin D deficiency
Andere Medikamente: Metoprolol XR 200mg Amitriptyline 25mg Vitamin D3 500IU Multivitamin Omerprazole 40mg
Allergien: pineapple, venison, red grapes, Biaxin, Zoloft, Zofran, Effexor, Ultram (any SSRI due to a serotonin syndrome diagnosis)
Vorherige Impfungen: -

VAERS 1984361

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: NY
Alter: 79,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 21.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site erythema Injection site pruritus Rash

Symptomtext

Site: Itching at Injection Site-Mild, Site: Redness at Injection Site-Mild, Systemic: Allergic: Rash Generalized-Mild, Additional Details: Patient presented 6 days later stating he just started having a rash on his arm where the injection took place. It was his 3rd dose but previously had the pfizer vaccine for his first 2 doses

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1981545

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: MA
Alter: 50,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Blood pressure increased Headache Pain

Symptomtext

I had light body aches the day of vaccination and a headache. The next morning, Saturday, the headache was aching more and I felt my blood pressure was raising. I was checked my blood pressure and noticed it was higher than normal. I called my PCP and was told to come in on Monday for examination. By Monday, the body aches were gone but I still had a headache and my BP was still high; my PCP increased my losartan dosage from 25mg to 50mg. By Thursday, my BP was still pretty high so I contacted my PCP again and he increased my losartan dosage again from 50mg to 75mg which helped reduce and drop my BP back to normal. My BP has never spiked like this before until after the vaccine; I don't want to blame the vaccine, but it's pretty coincidental.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Losartan 25mg, Allerga
Allergien: Compazine
Vorherige Impfungen: -

VAERS 1975272

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: TX
Alter: 60,0
Geschlecht: M
Eingang: 23.12.2021
Impfdatum: 21.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Arthralgia Headache

Symptomtext

Joint Aches and pain. Fever of 99 for 2 days. Mild headache

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Mild Asthma
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1974497

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: NY
Alter: 50,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site erythema Injection site pain

Symptomtext

Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1971757

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 54,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Erythema Pruritus Skin warm

Symptomtext

Arm red and warm to touch, and itching started next day. Still itching 5 days later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None known
Vorherige Impfungen: -

VAERS 1971178

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: FL
Alter: 66,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Atrial fibrillation Extra dose administered Incorrect route of product administration Malaise

Symptomtext

Nurse shot the vaccine needle into the side of my head by accident - Then I took another shot in my arm. Not feeling the greastest as I also have AFib heart and will consult w my Primary Care Doc

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: small cold cough
Vorgeschichte: NA
Andere Medikamente: Pro Air - Wexela 250
Allergien: NO
Vorherige Impfungen: -

VAERS 1970964

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 36,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Dizziness

Symptomtext

Systemic: Dizziness/Lightheadedness-Mild, Additional Details: Patient felt dizzy after the vaccine and stayed in the clinic for 30 minutes. VSS. Patient left after dizziness went away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1968661

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: TX
Alter: 25,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: N/A
Route/Site: ID / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Feeling abnormal Heart rate increased Incorrect route of product administration Injection site pruritus Wrong product administered

Symptomtext

Accidentally administered 0.1 of moderna vaccine intradermally instead of tubersol for TB skin test. Patient reported that arm was itching where bleb was formed. Patient with known history of anxiety began to feel strange. heart rate went up to 130, but quickly returned to 80s after deep breathing and parent came to bedside for comfort. Patient's BP was in 130s/80s. No airway compromise or difficulty breathing, sats 99-100%. Patient was observed for 1 hour, given 25 mg of benadryl, and left with father. Given ED precautions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pruritus
Hospital-Tage: -
Labordaten: vital signs
Aktuelle Erkrankungen: n/a
Vorgeschichte: n/a
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1967759

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NJ
Alter: 32,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 20.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Arthralgia Chills Injection site pain Nausea Pain in extremity

Symptomtext

chills, very achy around the injection site but also in my legs, hips, nausea

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Wellbutrin
Allergien: N/A
Vorherige Impfungen: Moderna 2nd dose covid, 5/3/21, chills, aches, fever

VAERS 1967433

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: NM
Alter: 49,0
Geschlecht: F
Eingang: 21.12.2021
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Influenza Injection site pain Lymphadenitis Lymphadenopathy Nasopharyngitis Vaccine positive rechallenge

Symptomtext

Cold and flu symptoms, swelling and inflammation of the lymph nodes under arm, soreness at injection site. Same symptoms happened after 2nd dose and 3rd dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Arthritis, chronic kidney condition.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: -

VAERS 1963685

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: NY
Alter: 87,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Injection site pain

Symptomtext

Site: Pain at Injection Site-Mild

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1962302

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

mild

Staat: MO
Alter: 68,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 17.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site pain

Symptomtext

Site: Pain at Injection Site-Severe

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1998665

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

mild

Staat: CA
Alter: 70,0
Geschlecht: F
Eingang: 08.09.2021
Impfdatum: 27.12.2021
Beginn: 27.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Injection site erythema Injection site swelling

Symptomtext

Swelling and Redness at injected site/ left deltoid. Occurred at night on 12/7/27/21.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: xanax, dichcline, simvastatin, aspirin, acetaminophen
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2680503

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: AR
Alter: 64,0
Geschlecht: F
Eingang: 08.09.2023
Impfdatum: 18.03.2022
Beginn: 30.08.2023
Tage bis Beginn: 530,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19

Symptomtext

hospitalized with covid; fully vaccinated with 1 booster

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: unknown
Vorgeschichte: Cancer (cervical and ovarian), COPD, Hyperlipidemia, Hypertension and Reflux
Andere Medikamente: unknown
Allergien: meclizine
Vorherige Impfungen: -

VAERS 2668520

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 09.08.2023
Impfdatum: 23.01.2022
Beginn: 20.01.2023
Tage bis Beginn: 362,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Hypoxia

Symptomtext

HYPOXEMIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypoxia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2663463

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 86,0
Geschlecht: F
Eingang: 31.07.2023
Impfdatum: 05.04.2022
Beginn: 05.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered No adverse event

Symptomtext

No adverse event; HCP stated a vaccine that expired in 02-Apr-2022 was administered to patient on 05-Apr-2022, 3 days later; This spontaneous case was reported by a consumer and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP stated a vaccine that expired in 02-Apr-2022 was administered to patient on 05-Apr-2022, 3 days later) and NO ADVERSE EVENT (No adverse event) in an 86-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 05-Apr-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP stated a vaccine that expired in 02-Apr-2022 was administered to patient on 05-Apr-2022, 3 days later). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP stated a vaccine that expired in 02-Apr-2022 was administered to patient on 05-Apr-2022, 3 days later) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP stated a vaccine that expired in 02-Apr-2022 was administered to patient on 05-Apr-2022, 3 days later). It was unknown patient did receive any other vaccines in the 4 weeks prior to COVID-19 vaccine. No concomitant medication was reported. Dosage text reported as unknown. No treatment information was reported. This case was linked to US-MODERNATX, INC.-MOD-2023-734665 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-734665:Same Reporter ,Patient 2

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2663462

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 86,0
Geschlecht: M
Eingang: 31.07.2023
Impfdatum: 05.04.2022
Beginn: 05.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered No adverse event

Symptomtext

No adverse event; HCP stated a vaccine that expired in 02Apr2022 was administered to 2 patients on 05Apr2022; This spontaneous case was reported by a consumer and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (HCP stated a vaccine that expired in 02Apr2022 was administered to 2 patients on 05Apr2022) and NO ADVERSE EVENT (No adverse event) in an 86-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 prophylaxis. It was reported that HCP did not describe medical history or condition. It was reported that patient did not received any other vaccines in the 4 weeks prior to COVID-19 vaccine. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 05-Apr-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (HCP stated a vaccine that expired in 02Apr2022 was administered to 2 patients on 05Apr2022). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (HCP stated a vaccine that expired in 02Apr2022 was administered to 2 patients on 05Apr2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for EXPIRED PRODUCT ADMINISTERED (HCP stated a vaccine that expired in 02Apr2022 was administered to 2 patients on 05Apr2022). No concomitant medication was reported. Suspect product dosage text was reported as unknown. It was reported that patient received the second booster. This case is reported for patient 2. No treatment medication was reported. This case was linked to US-MODERNATX, INC.-MOD-2023-734675 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2023-734675:Same Reporter ,Patient 1

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: It was reported that HCP did not describe medical history or condition. It was reported that patient did not received any other vaccines in the 4 weeks prior to COVID-19 vaccine.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2652844

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 05.07.2023
Impfdatum: 26.12.2021
Beginn: 16.06.2023
Tage bis Beginn: 537,0
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 Pfizer 3/5/21 lot# EN6206; Pfizer 3/26/21 lot# ER8732; Moderna 12/26/21 lot# 068H21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2652829

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 33,0
Geschlecht: F
Eingang: 05.07.2023
Impfdatum: 14.01.2022
Beginn: 16.01.2022
Tage bis Beginn: 2,0
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 Pfizer 4/6/21 lot# EW0153; Pfizer 5/4/21 lot# Ew0171; Moderna 1/14/22 lot# 068H21A;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2635501

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 23.05.2023
Impfdatum: 05.01.2022
Beginn: 25.09.2022
Tage bis Beginn: 263,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute coronary syndrome Hypoxia

Symptomtext

ACUTE CORONARY SYNDROME, UNSPECIFIED HYPOXIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute coronary syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2631635

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

gering

Staat: TX
Alter: 60,0
Geschlecht: F
Eingang: 14.05.2023
Impfdatum: 17.12.2021
Beginn: 02.05.2023
Tage bis Beginn: 501,0
Dosis: UNK
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Musculoskeletal disorder

Symptomtext

Systemic: see below-Mild, Additional Details: daughter called and reported mom was having issues with arm vaccine was given in. Daughter stated her mom had vaccine administered in arm that she should not have due to lymph issues. Daughter did not state specifically what was wrong with arm other than she was having issues with it and believed it was due to covid vaccine received in 2021. At this time I have no other information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Musculoskeletal disorder
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2626452

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 85,0
Geschlecht: M
Eingang: 04.05.2023
Impfdatum: 06.01.2022
Beginn: 11.06.2022
Tage bis Beginn: 156,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Chronic respiratory failure Hypoxia

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE CHRONIC HYPOXEMIC RESPIRATORY FAILURE HYPOXIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chronic respiratory failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2624787

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 18.07.2022
Beginn: 03.08.2022
Tage bis Beginn: 16,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Hypoxia

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOXIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypoxia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2619032

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 67,0
Geschlecht: F
Eingang: 21.04.2023
Impfdatum: 09.01.2022
Beginn: 12.09.2022
Tage bis Beginn: 246,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Moderna 3/9/21 Lot# 010A21A; Moderna 4/6/21 Lot# 017B21A; Moderna 1/9/22 Lot# 068H21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2615222

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 66,0
Geschlecht: F
Eingang: 14.04.2023
Impfdatum: 19.12.2021
Beginn: 30.07.2022
Tage bis Beginn: 223,0
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 Janssen 4/10/21 Lot# 041A; Moderna 12/19/21 Lot# 068H21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2613841

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 57,0
Geschlecht: F
Eingang: 12.04.2023
Impfdatum: 21.12.2021
Beginn: 05.05.2022
Tage bis Beginn: 135,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Moderna 3/30/21 Lot# 018B21A; Moderna 4/27/21 Lot# 043B21A; Moderna 12/21/21 lot# 068H21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2609558

MODERNA · COVID19 (COVID19 (MODERNA BIVALENT)) · Charge 068H21A

gering

Staat: MI
Alter: 47,0
Geschlecht: F
Eingang: 05.04.2023
Impfdatum: -
Beginn: 10.09.2021
Tage bis Beginn: -
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: ja ER: unbekannt Erholt: nein

SARS-CoV-2 test Skin hyperpigmentation

Symptomtext

epidermal hyperpigmentation to bilateral lower extremities,dense multiple dark brown macules; This spontaneous case was reported by a nurse and describes the occurrence of SKIN HYPERPIGMENTATION (epidermal hyperpigmentation to bilateral lower extremities,dense multiple dark brown macules) in a 47-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch no. 068H21A) for COVID-19 prophylaxis. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for an unknown indication. The patient's past medical history included Concussion. Concurrent medical conditions included Rhinitis seasonal, Hypothyroidism, Migraine, Penicillin allergy, Sulfonamide allergy (Sulfa), Drug allergy (Compazine), Seafood allergy (Shrimp.) and Insect bite allergy (Vespids). Concomitant products included CETIRIZINE HYDROCHLORIDE (ZYRTEC [CETIRIZINE HYDROCHLORIDE]), AMANTADINE, LEVOTHYROXINE SODIUM (SYNTHROID), FLUTICASONE PROPIONATE (FLONASE [FLUTICASONE PROPIONATE]) and VITAMIN D NOS for an unknown indication. On an unknown date, the patient received fourth dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form and fifth dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On an unknown date, received third dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) dosage was changed to 1 dosage form, second dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) dosage was changed to 1 dosage form and first dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) dosage was changed to 1 dosage form. On 10-Sep-2021, the patient experienced SKIN HYPERPIGMENTATION (epidermal hyperpigmentation to bilateral lower extremities,dense multiple dark brown macules) (seriousness criterion disability). At the time of the report, SKIN HYPERPIGMENTATION (epidermal hyperpigmentation to bilateral lower extremities,dense multiple dark brown macules) had resolved with sequelae. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 18-Jul-2022, SARS-CoV-2 test: (Positive) Nasal Swab. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter did not provide any causality assessments. The race of the patient reported. The vaccination site for Dose 4 of Moderna and other doses of Pfizer vaccine was provided as Deltoid. Patient had received the most recent vaccine dose in hospital. Patient had received the treatment for the events and had visited the Dermatology for the same. It was reported that the patient had not tested positive for COVID-19 vaccine prior to receiving the COVID-19 vaccine. Since the vaccination, the patient has been tested for COVID-19 reported as Yes. Company comment- This is a spontaneous case concerning a 47-year-old-female-patient with no relevant medical history who experienced the serious (disability) unexpected event of skin hyperpigmentation (reported as epidermal hyperpigmentation to bilateral lower extremities, dense multiple dark brown macules). A dose of mRNA-1273.222 (Original/Omicron BA.4/5) vaccine, given as a fourth dose of COVID vaccine schedule, was administered. Temporal association cannot be assessed due to lack of information on vaccination date. Four doses of TOZINAMERAN vaccine, given as first, second, third and fifth doses were given (revaccination with different COVID-19 vaccine and interchange of vaccine products). No further details were provided for medical review. The benefit-risk relationship of mRNA-1273.222 (Original/Omicron BA.4/5) vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: SARS-CoV-2 test
Hospital-Tage: -
Labordaten: Test Date: 20220718; Test Name: PCR; Test Result: Positive ; Result Unstructured Data: Nasal Swab
Aktuelle Erkrankungen: Drug allergy (Compazine); Hypothyroidism; Insect bite allergy (Vespids); Migraine; Penicillin allergy; Rhinitis seasonal; Seafood allergy (Shrimp.); Sulfonamide allergy (Sulfa)
Vorgeschichte: Medical History/Concurrent Conditions: Concussion
Andere Medikamente: ZYRTEC [CETIRIZINE HYDROCHLORIDE]; AMANTADINE; SYNTHROID; FLONASE [FLUTICASONE PROPIONATE]; VITAMIN D NOS
Allergien: -
Vorherige Impfungen: -

VAERS 2609330

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 62,0
Geschlecht: M
Eingang: 04.04.2023
Impfdatum: 21.12.2021
Beginn: 01.11.2022
Tage bis Beginn: 315,0
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 Pfizer 4/16/21 Lot# Ew0158; Pfizer 5/13/21 Lot# Ew0186; 12/21/21 Moderna Lot# 068H21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2607936

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: -
Geschlecht: F
Eingang: 01.04.2023
Impfdatum: -
Beginn: 18.07.2022
Tage bis Beginn: -
Dosis: 4
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective SARS-CoV-2 test

Symptomtext

PCR covid test date=18Jul2022, covid test result=Positive; Pfizer Dose 1, 2, 3; PCR covid test date=18Jul2022, covid test result=Positive; Pfizer Dose 1, 2, 3; This is a spontaneous report received from contactable reporter(s) (Nurse). The reporter is the patient. A 47-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), as dose 1, single (Lot number: EL0140), as dose 2, single (Lot number: EL3249) and as dose 3 (booster), single (Lot number: EW0183) for covid-19 immunisation; elasomeran (MODERNA COVID-19 VACCINE), as dose 4 (booster), single (Lot number: 068H21A) for covid-19 immunisation. The patient's relevant medical history included: "Known allergies: Shrimp" (unspecified if ongoing); "Known allergies: PCN" (unspecified if ongoing); "Known allergies: Vespids" (unspecified if ongoing); "Migraines" (unspecified if ongoing); "Sessional rhinitis" (unspecified if ongoing); "Hx concussion" (unspecified if ongoing); "Hypothyroid" (unspecified if ongoing); "Known allergies: Sulfa" (unspecified if ongoing). The patient's concomitant medications were not reported. Past drug history included: Compazine, reaction(s): "allergies". The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 18Jul2022, outcome "unknown" and all described as "PCR covid test date=18Jul2022, covid test result=Positive; Pfizer Dose 1, 2, 3". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (18Jul2022) Positive, notes: Nasal Swab.; Sender's Comments: Linked Report(s) : US-PFIZER INC-202300135046 same reporter/patient/product, different dose/event;

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220718; Test Name: PCR; Test Result: Positive ; Comments: Nasal Swab
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy to insect sting; Concussion; Hypothyroidism; Migraine; Penicillin allergy; Seafood allergy; Seasonal rhinitis; Sulfonamide allergy
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2564921

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CT
Alter: -
Geschlecht: M
Eingang: 21.01.2023
Impfdatum: 20.12.2021
Beginn: 20.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Biopsy COVID-19 immunisation Eczema Interchange of vaccine products

Symptomtext

he started with Eczema and dermatitis/ confirmed diagnosis of Spongiotic Dermatitis; Revaccination with different COVID-19 vaccine; Interchange of vaccine products; This spontaneous case was reported by a consumer and describes the occurrence of ECZEMA (he started with Eczema and dermatitis/ confirmed diagnosis of Spongiotic Dermatitis), COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) in an adult male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 011B224 and 068H21A) for COVID-19 prophylaxis. Previously administered products included for Drug use for unknown indication: J&J COVID-19 (First Primary dose) on 09-Mar-2021. Past adverse reactions to the above products included No adverse event with J&J COVID-19. On 20-Dec-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 30-Jul-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 20-Dec-2021, the patient experienced COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products). On 21-Aug-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced ECZEMA (he started with Eczema and dermatitis/ confirmed diagnosis of Spongiotic Dermatitis). The patient was treated with CLOBETASOL for Spongiotic dermatitis, at an unspecified dose and frequency and DUPILUMAB (DUPIXENT) for Spongiotic dermatitis, at a dose of UNK UNK, q2wk. At the time of the report, ECZEMA (he started with Eczema and dermatitis/ confirmed diagnosis of Spongiotic Dermatitis) had not resolved and COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In November 2022, Biopsy: the doctor confirmed diagnosis of Spongiotic Dermatitis. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not reported. It was reported that within 2-3 weeks after shot 3 in AUG2022, patient started with Eczema and dermatitis. The dermatologist tried different topical steroids; last one was Clobetasol topical which did not help.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Biopsy
Hospital-Tage: -
Labordaten: Test Date: 202211; Test Name: biopsy; Result Unstructured Data: the doctor confirmed diagnosis of Spongiotic Dermatitis
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2560106

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 62,0
Geschlecht: F
Eingang: 14.01.2023
Impfdatum: 20.12.2021
Beginn: 05.01.2022
Tage bis Beginn: 16,0
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 three vaccines Moderna 2/24/21 Lot# 025A21A; Moderna 3/24/21 Lot# 028A21A; Moderna 12/20/21 Lot# 068H21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2540524

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 64,0
Geschlecht: F
Eingang: 22.12.2022
Impfdatum: 11.01.2022
Beginn: 21.12.2022
Tage bis Beginn: 344,0
Dosis: 2
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 vaccine breakthrough case

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: covid+ 12/21/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2508386

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 15.11.2022
Impfdatum: 02.03.2021
Beginn: 21.09.2022
Tage bis Beginn: 568,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Fall Limb injury SARS-CoV-2 test positive

Symptomtext

09/21/22 presents to ED for "fall" "leg injury". PMHx of "dementia, HLD, HTN, DMT2"

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 09/21/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2454731

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 22.09.2022
Impfdatum: 11.03.2021
Beginn: 10.09.2022
Tage bis Beginn: 548,0
Dosis: 3
Route/Site: UN / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: ja

COVID-19 Hip arthroplasty Joint dislocation Patient uncooperative SARS-CoV-2 test positive

Symptomtext

Pt to ED 9/11 w/ c/o hip dislocation, pt COVID+ 9/10. Pt w/ even and unlabored respirations, AOx0 w/ response to painful stimuli. 9/12 pt is very uncooperative with care, to OR for Revision to a total hip arthroplasty. Post-surgery, pt is alert and oriented to 0. Not following commands, on room air. Pt discharged 9/14.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 4,0
Labordaten: see above
Aktuelle Erkrankungen: None
Vorgeschichte: Posterior dislocation of hip, closed, left, initial encounter (CMS/HCC); Injury of left hip; COVID-19 virus infection
Andere Medikamente: Amitriptyline (ELAVIL); Cholecalciferol; Gabapentin (NEURONTIN); Hydrocodone-Acetaminophen Mirtazapine (REMERON); Omeprazole (PRILOSEC).
Allergien: None
Vorherige Impfungen: -

VAERS 2433617

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 38,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 13.04.2021
Beginn: 26.08.2022
Tage bis Beginn: 500,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Delivery Maternal exposure before pregnancy Pregnancy SARS-CoV-2 test positive

Symptomtext

08/26/22 presents to EC ED for "SVD (spontaneous vaginal delivery)". PMHx of "fibromyalgia and fatigue"

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 08/26/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2417213

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 62,0
Geschlecht: F
Eingang: 22.08.2022
Impfdatum: 15.03.2022
Beginn: 18.08.2022
Tage bis Beginn: 156,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

COVID vaccine breakthrough case. Moderna 12/30/20, 01/27/21 and boosted 3/15/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Positive COVID test on 08/18/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2412303

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

gering

Staat: GA
Alter: 57,0
Geschlecht: M
Eingang: 16.08.2022
Impfdatum: 01.02.2022
Beginn: 24.06.2022
Tage bis Beginn: 143,0
Dosis: 4
Route/Site: SYR / AR

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough Covid

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Positive home Covid test
Aktuelle Erkrankungen: none.
Vorgeschichte: Colon removed. Liver transplant.
Andere Medikamente: Prograf, B12, Niacin, Calcium w/ D, Magnesium, Protonix, Ecotrin, multivitamin, probiotic
Allergien: none.
Vorherige Impfungen: -

VAERS 2411106

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 66,0
Geschlecht: M
Eingang: 15.08.2022
Impfdatum: 23.12.2021
Beginn: 13.08.2022
Tage bis Beginn: 233,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Inappropriate schedule of product administration SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

covid vaccine breakthrough case dose 1 Moderna 3/8/21 012A21A dose 2 Moderna 4/8/21 017B21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: covid+ on 8/13/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2402816

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 05.08.2022
Impfdatum: 01.02.2022
Beginn: 01.08.2022
Tage bis Beginn: 181,0
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 three vaccines Moderan 4/21/21 Lot# 043B21; Moderan 5/19/21 Lot# 033B21A; Moderna 2/1/22 Lot# 068H21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397226

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine was administered after beyond use date and CDC expiry date; Vaccine administered to patient past the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient past the expiration date) and PRODUCT STORAGE ERROR (Vaccine was administered after beyond use date and CDC expiry date) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient past the expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was administered after beyond use date and CDC expiry date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient past the expiration date) and PRODUCT STORAGE ERROR (Vaccine was administered after beyond use date and CDC expiry date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The vial was stored in standard freezer for the lot 068H21A with 2 degrees F high -1 degrees F low on 04-Jan-2022. The BUD date and CDC expiry date was reported as 02-Apr-2022. No treatment medication was reported. This case contains information for the eleventh of 45 patients described by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397223

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine was expired on 02-Apr-2022 and removed from fridge on 08-Apr-2022/ Vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low; Patient received the Moderna vaccine beyond the 30-day use by date/ Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received the Moderna vaccine beyond the 30-day use by date/ Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine was expired on 02-Apr-2022 and removed from fridge on 08-Apr-2022/ Vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received the Moderna vaccine beyond the 30-day use by date/ Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was expired on 02-Apr-2022 and removed from fridge on 08-Apr-2022/ Vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received the Moderna vaccine beyond the 30-day use by date/ Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine was expired on 02-Apr-2022 and removed from fridge on 08-Apr-2022/ Vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. It was reported that patient took vaccine on 08-Apr-2022, after the expiration date i.e on 02-Apr-2022. The BUD date was reported as 02-Apr-2022. The vaccine was moved from the fridge on 08-Apr-2022. No additional information provided. Date Stored in Standard Freezer for the lot 068H21A was 2 degrees F high -1 degrees F low on 04-JAN-2022. No treatment medication were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397218

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccines were stored after CDC expiry date; Vaccine administered to patients past 30-day use by date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patients past 30-day use by date) and PRODUCT STORAGE ERROR (Vaccines were stored after CDC expiry date) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patients past 30-day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines were stored after CDC expiry date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patients past 30-day use by date) and PRODUCT STORAGE ERROR (Vaccines were stored after CDC expiry date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. CDC expiry date was reported as 02-Apr-2022 for Lot-068H21A. Date Stored in Standard Freezer for the lot 068H21A was 2 degrees F high, -1 degrees F low on 01-Apr-2022. No treatment medication was reported. This case contains information for the 19 of 45 patients described by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397208

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low; Vaccine administered to 45 patients past 30-day use by date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered to 45 patients past 30-day use by date) and PRODUCT STORAGE ERROR (vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered to 45 patients past 30-day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered to 45 patients past 30-day use by date) and PRODUCT STORAGE ERROR (vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No Concomitant medications were provided. The vaccine was stored in standard freezer on 04-Jan-2022. No treatment medications were provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397203

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccines were stored after beyond use date and CDC expiry date; Vaccine was administered after beyond use date and CDC expiry date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after beyond use date and CDC expiry date) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after beyond use date and CDC expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after beyond use date and CDC expiry date) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. It was reported that patient took vaccine on 08-Apr-2022, after the CDC expiration date i.e on 02-Apr-2022.The BUD date was reported as 02-Apr-2022. All 45 patients were adults, who received the Moderna vaccine beyond the 30-day use by date and no additional information provided. Date Stored in Standard Freezer for the lot 068H21A was 2 degrees F high, -1 degrees F low on 04-Jan-2022. No treatment medication was reported. This case contains information for the 36th of 45 patients described by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397198

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022/ Doses was stored in standard freezer on 01Apr2022; Patient received the Moderna vaccine beyond the 30-day use by date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received the Moderna vaccine beyond the 30-day use by date) and PRODUCT STORAGE ERROR (Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022/ Doses was stored in standard freezer on 01Apr2022) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received the Moderna vaccine beyond the 30-day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022/ Doses was stored in standard freezer on 01Apr2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received the Moderna vaccine beyond the 30-day use by date) and PRODUCT STORAGE ERROR (Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022/ Doses was stored in standard freezer on 01Apr2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. It was reported that patient took vaccine on 08Apr2022, after the expiration date on 02Apr2022. The BUD date was reported as 02Apr2022. All 45 patients were adults, who received the Moderna vaccine beyond the 30 day use by date and no additional information provided. Doses was stored in standard freezer for the lot 068H21A with 2 degrees F high and minus 1 degrees flow on 01Apr2022 was reported. No treatment medication was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397193

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccines were stored after beyond use date and CDC expiry date; Vaccine was administered after beyond use date and CDC expiry date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after beyond use date and CDC expiry date) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after beyond use date and CDC expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after beyond use date and CDC expiry date) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. The BUD date and CDC expiry date was reported as 02-Apr-2022. The vial was stored in standard freezer for the lot 068H21A with 2 degrees F high -1 degrees F low on 14-Jan-2022. No treatment medication were reported. This case contains information for the thirty fourth of 45 patients described by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397191

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

vaccine was stored in a standard freezer after CDC expiration; Vaccine administered to patient past the expiration date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient past the expiration date) and PRODUCT STORAGE ERROR (vaccine was stored in a standard freezer after CDC expiration) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient past the expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vaccine was stored in a standard freezer after CDC expiration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient past the expiration date) and PRODUCT STORAGE ERROR (vaccine was stored in a standard freezer after CDC expiration) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment details were reported. It was reported that the vial administered was stored in standard freezer on 04-Jan-2022 with temperature 2 Degrees F high and -1 Degrees F low. This case contains information for the 33 of 45 patients described by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397187

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccines were stored after beyond use date and CDC expiry date; Vaccine administered to patient past 30-day use by date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient past 30-day use by date.) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient past 30-day use by date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient past 30-day use by date.) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The BUD date was reported as 02-Apr-2022. Date Stored in Standard Freezer for the lot 068H21A was 2 degrees F high, -1 degrees F low on 04-Jan-2022. No treatment medication was reported. This case contains information for the ninth of 45 patients described by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2022-571126 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-571126:Master case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397185

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccines were stored after beyond use date and CDC expiry date; Vaccine was administered after beyond use date and CDC expiry date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after beyond use date and CDC expiry date) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after beyond use date and CDC expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after beyond use date and CDC expiry date) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that the vial was stored in standard freezer for the lot 068H21A with 2 degrees F high -1 degrees F low on 04-Jan-2022. The beyond use date and CDC expiry date was reported as 02-Apr-2022. No treatment information was provided by the reporter. This case contains information for the eighth of 45 patients described by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2022-571126 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-571126:Master Case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397184

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccines were stored after beyond use date and CDC expiry date; Vaccine was administered after beyond use date and CDC expiry date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after beyond use date and CDC expiry date) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after beyond use date and CDC expiry date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was administered after beyond use date and CDC expiry date) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that the vial was stored in standard freezer for the lot 068H21A with 2 degrees F high -1 degrees F low on 04-Jan-2022. The beyond use date and CDC expiry date was reported as 02-Apr-2022. No treatment information was provided by the reporter. This case contains information for the thirtieth of 45 patients described by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2022-571126 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-571126:Master Case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397183

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccines were stored after beyond use date and expiry date; Vaccine administered to past 30-day use by date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered to past 30-day use by date.) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and expiry date) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered to past 30-day use by date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and expiry date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered to past 30-day use by date.) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and expiry date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. The date was reported as 02-APR-2022. The vial was stored in standard freezer for the lot 068H21A with 2 degrees F high and -1 degrees F low on 04-JAN-2022. No treatment medication were reported. This case contains information for the twenty ninth of 45 patients described by the reporter. This case was linked to US-MODERNATX, INC.-MOD-2022-571126 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-571126:Master case

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397182

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low; Patient received the Moderna vaccine beyond the 30-day use by date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received the Moderna vaccine beyond the 30-day use by date) and PRODUCT STORAGE ERROR (Vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received the Moderna vaccine beyond the 30-day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received the Moderna vaccine beyond the 30-day use by date) and PRODUCT STORAGE ERROR (Vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. The vaccines were stored in a standard freezer. A total of 45 doses from the outlined lot numbers were administered past the expiration date. Date vaccine stored in Standard Freezer on 01-Apr-2022. No treatment medications were reported. This case contains 7th patient information out of 45 patients.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397181

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Moderna vaccine stored beyond use by date; Vaccine administered to patient beyond use by date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient beyond use by date.) and PRODUCT STORAGE ERROR (Moderna vaccine stored beyond use by date) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient beyond use by date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Moderna vaccine stored beyond use by date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient beyond use by date.) and PRODUCT STORAGE ERROR (Moderna vaccine stored beyond use by date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not provided by the reporter. Date the vial was stored in standard freezer was 04-Jan-2022 (2 degrees F high -1 degrees F low) Treatment information was not provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397180

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 22.04.2022
Beginn: 22.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F lowon 4Jan2022; Vaccine administered to 45 patients past 30-day use by date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered to 45 patients past 30-day use by date) and PRODUCT STORAGE ERROR (vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F lowon 4Jan2022) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 22-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 22-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered to 45 patients past 30-day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F lowon 4Jan2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered to 45 patients past 30-day use by date) and PRODUCT STORAGE ERROR (vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F lowon 4Jan2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant drug information was provided. Vaccine was initially stored in refrigerator on 4Jan2022 and beyond used date for the product was 2Apr2022. No treatment drug information was provided. Case is reported for the sixth out of 45 patients who had received expired vaccine as reported by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397178

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccines were stored after beyond use date and CDC expiry date; Vaccine administered to patient past 30-day use by date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient past 30-day use by date.) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient past 30-day use by date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered to patient past 30-day use by date.) and PRODUCT STORAGE ERROR (Vaccines were stored after beyond use date and CDC expiry date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. This case contains information for the 5th of 45 female patients described by the reporter. No concomitant medication was reported. It was reported that patient took vaccine on 08-Apr-2022, after the expiration date i.e on 02-Apr-2022.The BUD date was reported as 02-Apr-2022. All 45 patients were adults, who received the Moderna vaccine beyond the 30-day use by date and no additional information provided. Date Stored in Standard Freezer for the lot 068H21A was 2 degrees F high, -1 degrees F low on 04-Jan-2022. No treatment medication was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397174

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022; Vaccine administered to 45 patients past 30-day use by date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered to 45 patients past 30-day use by date) and PRODUCT STORAGE ERROR (Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered to 45 patients past 30-day use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered to 45 patients past 30-day use by date) and PRODUCT STORAGE ERROR (Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The BUD date was reported as 02-Apr-2022. All 45 patients were adults, who received the Moderna vaccine beyond the 30-day use by date and no additional information was provided. Date Stored in Standard Freezer for the lot 068H21A was 2 degrees F (high), -1 degrees F (low) on 04-Jan-2022. No treatment information was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2397172

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 30.07.2022
Impfdatum: 11.05.2022
Beginn: 11.05.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low; Vaccine administered to 45 patients past 30-day use by date.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine administered to 45 patients past 30-day use by date.) and PRODUCT STORAGE ERROR (vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 11-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 11-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine administered to 45 patients past 30-day use by date.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine administered to 45 patients past 30-day use by date.) and PRODUCT STORAGE ERROR (vaccines were stored in a standard freezer but temperature 2 degrees F high -1 degrees F low) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. The vaccines were stored in a standard freezer. A total of 45 doses from the outlined lot numbers were administered past the expiration date. Date vaccine stored in Standard Freezer on 01-Apr-2022. No treatment medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2387318

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 18,0
Geschlecht: F
Eingang: 24.07.2022
Impfdatum: 21.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

This is a spontaneous report received from a contactable reporter(s) (Consumer or other non HCP). A 19-year-old female patient received BNT162b2 (BNT162B2), on 01Apr2021 as dose 1, single (Lot number: EP6955) and on 21Apr2021 as dose 2, single (Batch/Lot number: unknown, Expiration Date: 30Jun2021) at the age of 18 years for Covid-19 immunisation; CoviD-19 vaccine mRNA (mRNA 1273) (MODERNA COVID-19 VACCINE), as dose 3 (booster), single (Lot number: 068H21A) for Covid-19 immunisation. The patient's relevant medical history was not reported. There were no concomitant medications. The following information was reported: VACCINATION FAILURE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Person that had COVID Vaccination; first two vaccination from Pfizer and the third booster was from Moderna and she have now got the COVID". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: Positive, notes: tested positive for COVID. (within two weeks). Therapeutic measures were not taken as a result of Covid-19. Clinical course: The Pfizer employee stated that he/she was reporting on behalf of someone, the patient name (daughter) (Initial captured as withheld in the tab). Employee stated that the reason for missing lot numbers of COVID-19 Vaccine Pfizer was that it looked like the first dose is EP6955 and second looked like, it is the same lot (further not clarified hence, not captured in tab). The employee had some details of the patient. The reporter stated that the patient had medical condition in past, but now she had recovered. The patient did not receive any other vaccines within four weeks prior to the vaccination. Regarding the treatment that the patient did not take medication. The reporter did not had the expiration date for the second dose. The reporter stated that the mailing address was withheld. This report was a product complaint report. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: home test; Test Result: Positive; Comments: tested positive for COVID (within two weeks).
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2338864

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: TX
Alter: 63,0
Geschlecht: F
Eingang: 28.06.2022
Impfdatum: 26.12.2021
Beginn: 01.03.2022
Tage bis Beginn: 65,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: ja Erholt: nein

Chest X-ray abnormal Computerised tomogram thorax abnormal Limb discomfort Lymphadenitis Pulmonary mass

Symptomtext

I had just seen my chiropractor for an adjustment, and let him know I was having issues with my left jaw and left arm. At my chiropractors recommendation I went to see my Cardiologist who referred me to the ER for testing. At the ER they did an X-Ray and CAT Scan where they discovered a nodule on my left lung, which was less than 1 cm. My PCP stated that he has seen this in patients who have had COVID-19, which I have not had at any point. I am under observation at this time, and will be having follow up CAT Scan in the fall. My lymph gland in my left breast area is still inflamed after beginning my COVID-19 vaccine series.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest X-ray abnormal
Hospital-Tage: -
Labordaten: X-Ray showed nodule on left lung less than 1cm on 03/01/2022 CAT Scan confirmed nodule on left lung on 03/01/2022
Aktuelle Erkrankungen: No
Vorgeschichte: Sjogren's Syndrome, Sleep Apnea, Mascular Degeneration, Anxiety, Posterior Zitreous Detachment, Hiatal Hernia, Mild Asthma
Andere Medikamente: Levothyroxine, Liothyronine, Bias hormone cream, Progesterone, Restasis, Custom Mixed Allergy Eye drops, Calcium, Vitamin D3, Mega Red, Magnesium, I-caps, L-thymine
Allergien: Aleve, sensitive to Amoxicillin, Humira
Vorherige Impfungen: Moderna Dose 1&2 resulted in swollen lymph gland in left breast area that is being monitored.

VAERS 2331678

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 38,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 05.04.2022
Beginn: 05.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine given after expiration date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2331676

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 61,0
Geschlecht: M
Eingang: 24.06.2022
Impfdatum: 18.04.2022
Beginn: 18.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine given after expiration date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2331672

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 75,0
Geschlecht: M
Eingang: 24.06.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine administered after expiration date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2331668

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 78,0
Geschlecht: F
Eingang: 24.06.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine was given after expiration date.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2331651

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 83,0
Geschlecht: M
Eingang: 24.06.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: IM / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Dose Given after Expiration Date

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2325176

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 33,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Individual were administered Moderna vaccine booster dose after the published expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date) in a 33-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date) outcome 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 details was not reported by the reporter. Reporter has not yet contacted patients for follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2325175

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Expired vaccine used/ Individual were administered Moderna vaccine booster dose after the published expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used/ Individual were administered Moderna vaccine booster dose after the published expiration date) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used/ Individual were administered Moderna vaccine booster dose after the published expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used/ Individual were administered Moderna vaccine booster dose after the published expiration date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication was provided Treatment medication was not provided by the reporter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2325173

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 54,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Expired vaccine used; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) in a 54-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine used). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine used) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant product reported by reporter. No treatment medication reported by reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2325172

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 74,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Individual were administered Moderna vaccine booster dose after the published expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 06-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date) outcome 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 details was not reported by the reporter. Reporter has not yet contacted patients for follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2325171

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 84,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 05.04.2022
Beginn: 05.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Individual were administered Moderna vaccine booster dose after the published expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date) in an 84-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 05-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date) outcome 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. Patient received booster dose. Treatment details was not reported by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2325170

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 76,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Individual were administered Moderna vaccine booster dose after the published expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date) in a 76-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication 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: -

VAERS 2325168

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 65,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Individual were administered Moderna vaccine booster dose after the published expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date) outcome 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 details was not reported by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2325167

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 76,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Individuals were administered Moderna vaccine booster doses after the published expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Individuals were administered Moderna vaccine booster doses after the published expiration date) in a 76-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 prophylaxis. No Medical History information was reported. On 04-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 04-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Individuals were administered Moderna vaccine booster doses after the published expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Individuals were administered Moderna vaccine booster doses after the published expiration date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), 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: -

VAERS 2325166

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 77,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 03.04.2022
Beginn: 03.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

administered Moderna vaccine booster doses after the published expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered Moderna vaccine booster doses after the published expiration date) in a 77-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered Moderna vaccine booster doses after the published expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administered Moderna vaccine booster doses after the published expiration date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant drug information was provided. No treatment drug information was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2325164

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 59,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 03.04.2022
Beginn: 03.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Individual were administered Moderna vaccine booster dose after the published expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Individual were administered Moderna vaccine booster dose after the published expiration date) outcome 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 details was not reported by the reporter. Reporter has not yet contacted patients for follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2325157

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 59,0
Geschlecht: F
Eingang: 21.06.2022
Impfdatum: 03.04.2022
Beginn: 03.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Moderna vaccine was placed in the refrigerator on 24APR2022 and had a 30 day beyond use date of 23APR2022/Focusing on the Use by date administered vaccine past the Manufacturers expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Moderna vaccine was placed in the refrigerator on 24APR2022 and had a 30 day beyond use date of 23APR2022/Focusing on the Use by date administered vaccine past the Manufacturers expiration date) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Moderna vaccine was placed in the refrigerator on 24APR2022 and had a 30 day beyond use date of 23APR2022/Focusing on the Use by date administered vaccine past the Manufacturers expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Moderna vaccine was placed in the refrigerator on 24APR2022 and had a 30 day beyond use date of 23APR2022/Focusing on the Use by date administered vaccine past the Manufacturers expiration date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. The reporter stated that lot number 068H21A which expired on 02-APR-2022 was placed in the refrigerator on 24-Mar-2022 and had a 30 day beyond use date of 23-Apr-2022. Focusing on the Use by date the vaccine was administered past the Manufacturers expiration date to the patient. The patient received the booster dose. It was also reported that the vial had not undergone any temperature excursions. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 17-Jun-2022: Significant Live follow-up was received with patient information and suspect drug information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323528

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 59,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 03.04.2022
Beginn: 03.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Expired vaccine administered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323526

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 17.06.2022
Impfdatum: 03.04.2022
Beginn: 03.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Expired vaccine administered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323525

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 77,0
Geschlecht: M
Eingang: 17.06.2022
Impfdatum: 03.04.2022
Beginn: 03.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Expired vaccine administered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323524

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 17.06.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Expired vaccine administered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323521

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Expired vaccine administered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323519

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 76,0
Geschlecht: M
Eingang: 17.06.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Expired vaccine administered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323517

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 84,0
Geschlecht: M
Eingang: 17.06.2022
Impfdatum: 05.04.2022
Beginn: 05.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Expired vaccine administered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323516

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 54,0
Geschlecht: M
Eingang: 17.06.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Expired vaccine administered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323513

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 65,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Expired vaccine administered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323512

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 17.06.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Expired vaccine administered

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2323267

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 74,0
Geschlecht: M
Eingang: 17.06.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Injected expired vaccine

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2308789

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 07.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

VACCINE ADMINISTERED AFTER LOT EXPIRATION DATE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2308739

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 36,0
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 21.04.2022
Beginn: 21.04.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

VACCINE ADMINISTERED AFTER LOT EXPIRATION DATE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2308735

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 39,0
Geschlecht: M
Eingang: 03.06.2022
Impfdatum: 21.04.2022
Beginn: 21.04.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

VACCINE ADMINISTERED AFTER LOT EXPIRATION DATE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2308732

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 44,0
Geschlecht: M
Eingang: 03.06.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

VACCINE ADMINISTERED AFTER LOT EXPIRATION DATE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2308719

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 49,0
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 11.04.2022
Beginn: 11.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

VACCINE ADMINISTERED AFTER LOT EXPIRATION DATE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2308704

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 73,0
Geschlecht: M
Eingang: 03.06.2022
Impfdatum: 13.04.2022
Beginn: 13.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

VACCINE ADMINISTERED AFTER LOT EXPIRATION DATE.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2301437

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 33,0
Geschlecht: F
Eingang: 28.05.2022
Impfdatum: 06.04.2021
Beginn: 08.11.2021
Tage bis Beginn: 216,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abortion spontaneous

Symptomtext

After two full term pregnancies in 2018 and 2019, I had three miscarriages in six months. The only change in my life was getting the COVID-19 vaccine (Pfizer 1 and 2 and Moderna booster). Miscarriages all occurred at 5 weeks. Here are the dates: November 8, 2021 January 30, 2022 May 22, 2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abortion spontaneous
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: prenatal vitamin
Allergien: none
Vorherige Impfungen: -

VAERS 2293128

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NV
Alter: 38,0
Geschlecht: U
Eingang: 28.05.2022
Impfdatum: 20.04.2022
Beginn: 20.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: - / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022; Patient received vaccine on 20-Apr-2022 which had got expired vaccine on 02-Apr-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine on 20-Apr-2022 which had got expired vaccine on 02-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022) in a 38-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022 at 2:03 PM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 20-Apr-2022 at 2:03 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine on 20-Apr-2022 which had got expired vaccine on 02-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine on 20-Apr-2022 which had got expired vaccine on 02-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant mediations were not reported. Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022 The vial did not undergo any temperature excursion. The reporter confirmed no side effects were reported. Treatment information was not reported

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2293128

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NV
Alter: 38,0
Geschlecht: U
Eingang: 28.05.2022
Impfdatum: 20.04.2022
Beginn: 20.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022; Patient received vaccine on 20-Apr-2022 which had got expired vaccine on 02-Apr-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received vaccine on 20-Apr-2022 which had got expired vaccine on 02-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022) in a 38-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022 at 2:03 PM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 20-Apr-2022 at 2:03 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received vaccine on 20-Apr-2022 which had got expired vaccine on 02-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received vaccine on 20-Apr-2022 which had got expired vaccine on 02-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant mediations were not reported. Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022 The vial did not undergo any temperature excursion. The reporter confirmed no side effects were reported. Treatment information was not reported

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2293176

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NV
Alter: 29,0
Geschlecht: U
Eingang: 27.05.2022
Impfdatum: 06.05.2022
Beginn: 06.05.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 2-Apr-2022 and Removed from freezer on 6-May-2022; Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 2-Apr-2022 and Removed from freezer on 6-May-2022) in a 29-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-May-2022 at 4:41 PM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 06-May-2022 at 4:41 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 2-Apr-2022 and Removed from freezer on 6-May-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 2-Apr-2022 and Removed from freezer on 6-May-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant product was provided by the reporter. No treatment medication was provided. No temperature excursion reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2293176

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NV
Alter: 29,0
Geschlecht: U
Eingang: 27.05.2022
Impfdatum: 06.05.2022
Beginn: 06.05.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 2-Apr-2022 and Removed from freezer on 6-May-2022; Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 2-Apr-2022 and Removed from freezer on 6-May-2022) in a 29-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-May-2022 at 4:41 PM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 06-May-2022 at 4:41 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 2-Apr-2022 and Removed from freezer on 6-May-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 2-Apr-2022 and Removed from freezer on 6-May-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant product was provided by the reporter. No treatment medication was provided. No temperature excursion reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2293163

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NV
Alter: 63,0
Geschlecht: U
Eingang: 27.05.2022
Impfdatum: 05.05.2022
Beginn: 05.05.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 2-apr-2022 and was removed from freezer on 5-may-2022; Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 2-apr-2022 and was removed from freezer on 5-may-2022) in a 63-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 05-May-2022 at 2:00 PM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 05-May-2022 at 2:00 PM, after starting mRNA-1273 (Spikevax), the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 2-apr-2022 and was removed from freezer on 5-may-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 2-apr-2022 and was removed from freezer on 5-may-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. The vaccine was removed from the freezer on 05-May-2022. The reporter confirmed no side effects were reported. No temperature excursion occurred. No treatment information was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2293163

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NV
Alter: 63,0
Geschlecht: U
Eingang: 27.05.2022
Impfdatum: 05.05.2022
Beginn: 05.05.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 2-apr-2022 and was removed from freezer on 5-may-2022; Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 2-apr-2022 and was removed from freezer on 5-may-2022) in a 63-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 05-May-2022 at 2:00 PM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 05-May-2022 at 2:00 PM, after starting mRNA-1273 (Spikevax), the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 2-apr-2022 and was removed from freezer on 5-may-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 2-apr-2022 and was removed from freezer on 5-may-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. The vaccine was removed from the freezer on 05-May-2022. The reporter confirmed no side effects were reported. No temperature excursion occurred. No treatment information was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2293148

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NV
Alter: 39,0
Geschlecht: U
Eingang: 27.05.2022
Impfdatum: 20.04.2022
Beginn: 20.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022; Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022) in a 39-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022 at 3:26 PM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 20-Apr-2022 at 3:26 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant product use was provided. No treatment medication was provided. No temperature excursion reported. On 20 Apr 2022, vaccine was removed from freezer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2293148

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NV
Alter: 39,0
Geschlecht: U
Eingang: 27.05.2022
Impfdatum: 20.04.2022
Beginn: 20.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022; Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022) in a 39-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022 at 3:26 PM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 20-Apr-2022 at 3:26 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was removed from freezer on 20-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant product use was provided. No treatment medication was provided. No temperature excursion reported. On 20 Apr 2022, vaccine was removed from freezer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2293117

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NV
Alter: 35,0
Geschlecht: U
Eingang: 27.05.2022
Impfdatum: 20.04.2022
Beginn: 20.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 02-Apr-2022 and removed from freezer on 20-Apr-2022; Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and removed from freezer on 20-Apr-2022) in a 35-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022 at 2:29 PM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 20-Apr-2022 at 2:29 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and removed from freezer on 20-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and removed from freezer on 20-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant mediations were not reported. No temperature excursion reported. The reporter confirmed no side effects were reported. Treatment information was not reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2293117

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NV
Alter: 35,0
Geschlecht: U
Eingang: 27.05.2022
Impfdatum: 20.04.2022
Beginn: 20.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 02-Apr-2022 and removed from freezer on 20-Apr-2022; Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and removed from freezer on 20-Apr-2022) in a 35-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 20-Apr-2022 at 2:29 PM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 20-Apr-2022 at 2:29 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and removed from freezer on 20-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and removed from freezer on 20-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant mediations were not reported. No temperature excursion reported. The reporter confirmed no side effects were reported. Treatment information was not reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2295584

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 26.05.2022
Impfdatum: 21.12.2021
Beginn: 17.05.2022
Tage bis Beginn: 147,0
Dosis: 3
Route/Site: OT / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Interchange of vaccine products SARS-CoV-2 test

Symptomtext

Interchange of vaccine products; tested positive again; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (tested positive again) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Pfizer / BioNTech (Dose Number: 1 Batch/Lot No: Unknown. Misplaced/discarded Location of injection: Arm Left) on 13-Mar-2021 and Pfizer / BioNTech (Dose Number: 2 Batch/Lot No: Unknown. Misplaced/discarded Location of injection: Arm Left) on 03-Apr-2021. Past adverse reactions to the above products included No adverse event with Pfizer / BioNTech and Pfizer / BioNTech. Concurrent medical conditions included Drug allergy. On 21-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-May-2022 at 7:00 AM, the patient experienced COVID-19 (tested positive again). On an unknown date, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 08-May-2022 to 12-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, COVID-19 (tested positive again) was resolving and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 17-May-2022, SARS-CoV-2 test: positive (Positive) positive. In 2022, SARS-CoV-2 test: positive (Positive) positive, negative (Negative) Negative (on day five) and negative (Negative) Negative (on day six). She tested positive for Cove at 19 and took Paxelvid after four days of testing positive unpacked of it she tested negative for Covid on an antigen test on day five. She tested negative again on day six. She felt good and thought she was in the cleared. Four days after the first negative test she had all symptoms back and tested positive again No concomitant medication were reported. Company comment: This spontaneous case concerns a 43 year old female patient with no reported medical history, who experienced the unexpected non serious AESI of COVID-19, about 7 months and 4 days after receiving the third dose with mRNA-1273 vaccine in the COVID-19 vaccination series. The patient received the previous two doses with Pfizer vaccine, the last dose being given about 8 months and 18 days prior to mRNA-1273 vaccine, with no reported adverse events. Interchange of vaccine products was noted. She tested positive for Covid-19 and took Paxlovid after four days of testing positive; tested negative on the fifth day. Four days after the negative test, developed all the symptoms back and tested positive again. No further information on risk factors and co morbidities was available in the report. The event was resolving. The ongoing COVID-19 pandemic could be a risk factor for the event. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case concerns a 43 year old female patient with no reported medical history, who experienced the unexpected non serious AESI of COVID-19, about 7 months and 4 days after receiving the third dose with mRNA-1273 vaccine in the COVID-19 vaccination series. The patient received the previous two doses with Pfizer vaccine, the last dose being given about 8 months and 18 days prior to mRNA-1273 vaccine, with no reported adverse events. Interchange of vaccine products was noted. She tested positive for Covid-19 and took Paxlovid after four days of testing positive; tested negative on the fifth day. Four days after the negative test, developed all the symptoms back and tested positive again. No further information on risk factors and co morbidities was available in the report. The event was resolving. The ongoing COVID-19 pandemic could be a risk factor for the event. The benefit-risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220517; Test Name: COVID-19 antigen test; Test Result: Positive ; Result Unstructured Data: positive; Test Date: 2022; Test Name: COVID-19 antigen test; Test Result: Positive ; Result Unstructured Data: positive; Test Date: 2022; Test Name: COVID-19 antigen test; Test Result: Negative ; Result Unstructured Data: Negative (on day five); Test Date: 2022; Test Name: COVID-19 antigen test; Test Result: Negative ; Result Unstructured Data: Negative (on day six)
Aktuelle Erkrankungen: Drug allergy
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2294021

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 25.05.2022
Impfdatum: 11.04.2022
Beginn: 11.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

1 patient was administered expired vaccine on 11-Apr-2022, expiration was 02-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (1 patient was administered expired vaccine on 11-Apr-2022, expiration was 02-Apr-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 11-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (1 patient was administered expired vaccine on 11-Apr-2022, expiration was 02-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (1 patient was administered expired vaccine on 11-Apr-2022, expiration was 02-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2294020

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 25.05.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

1 patient was administered expired vaccine on 08-Apr-2022, CDC expiration was 02-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (1 patient was administered expired vaccine on 08-Apr-2022, CDC expiration was 02-Apr-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (1 patient was administered expired vaccine on 08-Apr-2022, CDC expiration was 02-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (1 patient was administered expired vaccine on 08-Apr-2022, CDC expiration was 02-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medications was not provided by the reporter. Reporter stated that they have reviewed historical storage records and can verify they were properly stored the entire duration of time on site. The vaccines were removed from the freezer on the day of each respective immunization. Treatment information was not provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2294017

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 25.05.2022
Impfdatum: 07.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

1 patient was administered expired vaccine on 07-Apr-2022, CDC expiration was 02-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (1 patient was administered expired vaccine on 07-Apr-2022, CDC expiration was 02-Apr-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 07-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 07-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (1 patient was administered expired vaccine on 07-Apr-2022, CDC expiration was 02-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (1 patient was administered expired vaccine on 07-Apr-2022, CDC expiration was 02-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. 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: -

VAERS 2292393

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 24.05.2022
Impfdatum: 08.04.2022
Beginn: 08.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine was expired on 02-Apr-2022 and removed from fridge on 08-Apr-2022.; Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022.) and PRODUCT STORAGE ERROR (Vaccine was expired on 02-Apr-2022 and removed from fridge on 08-Apr-2022.) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 08-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was expired on 02-Apr-2022 and removed from fridge on 08-Apr-2022.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was expired on 02-Apr-2022 and patient administered on 08-Apr-2022.) and PRODUCT STORAGE ERROR (Vaccine was expired on 02-Apr-2022 and removed from fridge on 08-Apr-2022.) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. It was reported that patient took vaccine on 08-Apr-2022, after the expiration date i.e on 02-Apr-2022.The BUD date was reported as 02-Apr-2022. The vaccine was moved from the fridge on 08-Apr-2022. It was reported that the vaccines were stored in the freezer and only removed as needed to thaw and then administered. The reporter doesn't have the information about the date the vial was 1st moved from the freezer to refrigerator. The vial was taken out at a time and thaw as they don't thaw enter box. No treatment medication were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2292392

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 24.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 02-Apr-2022 and removed from the fridge on 06-Apr-2022; Patient administered vaccine on 06-Apr-2022 past the BUD date 02-Apr-2022.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 06-Apr-2022 past the BUD date 02-Apr-2022.) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and removed from the fridge on 06-Apr-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 06-Apr-2022 past the BUD date 02-Apr-2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and removed from the fridge on 06-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient administered vaccine on 06-Apr-2022 past the BUD date 02-Apr-2022.) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and removed from the fridge on 06-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medication information was not provided by the reporter. The BUD date was reported as 02-Apr-2022. The vaccines were stored in the freezer and only removed as needed to thaw and then administered. It was mentioned that vials were taken out at a time and thawed as they did not thawed an entire box. Vaccine was removed from fridge on 06-Apr-2022. Treatment information was not provided by the reporter. This case was linked to MOD-2022-569375 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2290244

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 23.05.2022
Impfdatum: 05.04.2022
Beginn: 05.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 02-Apr-2022 and vaccine removed from fridge on 05-APR-2022; Vaccine expired on 02-Apr-2022 and vaccine administered on 05-APR-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 02-Apr-2022 and vaccine administered on 05-APR-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and vaccine removed from fridge on 05-APR-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 02-Apr-2022 and vaccine administered on 05-APR-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and vaccine removed from fridge on 05-APR-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 02-Apr-2022 and vaccine administered on 05-APR-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and vaccine removed from fridge on 05-APR-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. BUD date 02-APR-2022 and vaccination was removed from the fridge on 05-APR-22. No treatment information were provided. This case was linked to MOD-2022-569375.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2288999

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 21.05.2022
Impfdatum: 18.04.2022
Beginn: 18.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 02-Apr-2022 and vaccine removed from fridge on 18-Apr-2022; Vaccine expired on 02-Apr-2022 and vaccine administered on 18-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 02-Apr-2022 and vaccine administered on 18-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and vaccine removed from fridge on 18-Apr-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 18-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 18-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 02-Apr-2022 and vaccine administered on 18-Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and vaccine removed from fridge on 18-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine expired on 02-Apr-2022 and vaccine administered on 18-Apr-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and vaccine removed from fridge on 18-Apr-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Concomitant medication information was not provided by the reporter. The BUD date was reported as 02-Apr-2022. Vaccine was removed from fridge on 18-Apr-2022. Treatment information was not provided by the reporter. This case was linked to MOD-2022-571103, MOD-2022-571106 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 19-May-2022: Vaccine start date, expiry date and new event were added.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2287131

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 76,0
Geschlecht: M
Eingang: 20.05.2022
Impfdatum: 11.02.2022
Beginn: 10.05.2022
Tage bis Beginn: 88,0
Dosis: 1
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

Acute left ventricular failure COVID-19 Cardiac failure congestive Ejection fraction decreased SARS-CoV-2 test positive Transcatheter aortic valve implantation

Symptomtext

Pt was admitted for acute systolic CHF with an EF of 20 to 25% and has a life vest. The pt was scheduled for a TAVR at the facility on May 19. Prior to transfer to the facility he was tested for COVID and was positive with a CT value of 39.1. He was previously positive for COVID in December 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute left ventricular failure
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2286462

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NV
Alter: -
Geschlecht: U
Eingang: 20.05.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Administered expired Moderna vaccine; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered expired Moderna vaccine) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered expired Moderna vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered expired Moderna vaccine) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The HCP (health care professional) reported that an expired Moderna vaccine was administered to 36 patients from 15-Apr-2022 through 06-May-2022. The HCP confirmed no side effects 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: -

VAERS 2284530

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MS
Alter: 57,0
Geschlecht: F
Eingang: 19.05.2022
Impfdatum: 16.05.2022
Beginn: 16.05.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

an expired dose is given; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (an expired dose is given) in a 57-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 16-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 16-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (an expired dose is given). At the time of the report, EXPIRED PRODUCT ADMINISTERED (an expired dose is given) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Date the vial was initially stored in the refrigerator on 16MAY2022. The vial did not undergo any temperature excursions. No treatment information was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2283177

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MS
Alter: 57,0
Geschlecht: F
Eingang: 18.05.2022
Impfdatum: 16.05.2022
Beginn: 16.05.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

Pt given expired vaccine. No s/s. Contacted Moderna. Followed up with patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: None
Vorgeschichte: HTN, DM, obesity, GERD
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2280610

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 29,0
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: 28.12.2021
Beginn: 17.05.2022
Tage bis Beginn: 140,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: nein

Unevaluable event

Symptomtext

HOSPITALIZATION

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2277448

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CT
Alter: 71,0
Geschlecht: M
Eingang: 14.05.2022
Impfdatum: 01.04.2022
Beginn: 07.05.2022
Tage bis Beginn: 36,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 Drug ineffective

Symptomtext

Lack of drug effect; Covid Relapse; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (Covid Relapse) and DRUG INEFFECTIVE (Lack of drug effect) in a 71-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Pfizer / BioNTech (Dose Number: 3 Batch/Lot No: 30145BA) on 24-Sep-2021. Past adverse reactions to the above products included Allergy with Pfizer / BioNTech. Concurrent medical conditions included Hypertension and High cholesterol. On 01-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 22-Apr-2022, the patient received dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On 27-Apr-2022, received dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) dosage was changed to 1 dosage form. On 07-May-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced COVID-19 (Covid Relapse). On an unknown date, the patient experienced DRUG INEFFECTIVE (Lack of drug effect). At the time of the report, COVID-19 (Covid Relapse) had not resolved and DRUG INEFFECTIVE (Lack of drug effect) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications details were not reported by the reporter. The patient was taking other medications or products within 2 weeks of starting COVID-19 treatment. Patient received a COVID-19 vaccine previously. Device date was reported as 07-May-2022. Treatment details were not reported by the reporter. Company comment: This spontaneous case concerns a 71-year-old male patient with no reported medical history, who experienced the unexpected, serious (medically significant) adverse event of special interest COVID-19 (with a positive SARS-CoV-2 test) that occurred 36 days after receiving the fourth dose of mRNA-1273 Vaccine. Additionally, Drug ineffective was also reported. The patient was given a dose of Pfizer vaccine 10 days prior to the occurrence of the event. The event was conservatively considered as related since the temporal association cannot be assessed/excluded due to the limited information available. Details of concomitant medications, medical history, clinical course, treatment and outcome were not provided. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.; Sender's Comments: This spontaneous case concerns a 71-year-old male patient with no reported medical history, who experienced the unexpected, serious (medically significant) adverse event of special interest COVID-19 (with a positive SARS-CoV-2 test) that occurred 36 days after receiving the fourth dose of mRNA-1273 Vaccine. Additionally, Drug ineffective was also reported. The patient was given a dose of Pfizer vaccine 10 days prior to the occurrence of the event. The event was conservatively considered as related since the temporal association cannot be assessed/excluded due to the limited information available. Details of concomitant medications, medical history, clinical course, treatment and outcome were not provided. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: High cholesterol; Hypertension
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2271098

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 61,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 12.03.2021
Beginn: 27.01.2022
Tage bis Beginn: 321,0
Dosis: UNK
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 SARS-CoV-2 test positive Small intestinal obstruction

Symptomtext

01/27/22 presents to ED for "SBO (small bowel obstruction)". PMHx of "breast cancer, HTN, HLD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 01/27/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2270563

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 29,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 02-Apr-2022 and was stored in refrigerator on the day before administration; expired dose administered on 06-APR-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired dose administered on 06-APR-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was stored in refrigerator on the day before administration) in a 29-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired dose administered on 06-APR-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was stored in refrigerator on the day before administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired dose administered on 06-APR-2022) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was stored in refrigerator on the day before administration) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient received first booster dose of Moderna vaccine on 06-Apr-2022. Concomitant medication information was not provided. The vial was initially stored in the refrigerator on 05-Apr-2022. The healthcare provider had a lot number of the vial which they thought expired at a different time. However, when the healthcare provider entered the lot number on Moderna's online expiration tool look up, it was found that the lot had expired on 02-Apr-2022. The healthcare provider reported that each patient was administered with the dose from a different vial and each of the vial was stored in the refrigerator on the day before administration. The vial did not undergo any temperature excursions. It was reported that the patient had not reported of experiencing any adverse reactions to this expired dose. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 05-May-2022: Live Follow up received contained non significant information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2270562

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 23,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Expired vial was stored in the refrigerator the day before administration; expired doses administered to patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired doses administered to patients) and PRODUCT STORAGE ERROR (Expired vial was stored in the refrigerator the day before administration) in a 23-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 04-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired doses administered to patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Expired vial was stored in the refrigerator the day before administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired doses administered to patients) and PRODUCT STORAGE ERROR (Expired vial was stored in the refrigerator the day before administration) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No information on concomitant medication was reported. Patient received the first booster dose of Moderna vaccine on 04-Apr-2022 (Expiry date: 02-Apr-2022). It was reported that, the vials was initially stored in refrigerator a day before the administration and vials did not undergo any temperature excursions. The patient had not reported any adverse reactions to the dose. No information on treatment medications was reported. This case was linked to MOD-2022-558954 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 05-May-2022: Live follow up received contain no new information

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2270560

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 20,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 07.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine expired on 02-Apr-2022 and was stored in refrigerator on the day before administration; Expired dose was administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose was administered) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was stored in refrigerator on the day before administration) in a 20-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. Previously administered products included for COVID-19 vaccination: Pfizer (first dose) on 07-May-2021 and Pfizer (second dose) on 28-May-2021. Past adverse reactions to the above products included No adverse event with Pfizer and Pfizer. On 07-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 07-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose was administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was stored in refrigerator on the day before administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose was administered) and PRODUCT STORAGE ERROR (Vaccine expired on 02-Apr-2022 and was stored in refrigerator on the day before administration) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication information was not provided. The vial was initially stored in the refrigerator on 06-Apr-2022. The patient received first booster dose of Moderna vaccine on 07-Apr-2022. The healthcare provider had a lot number of the vial which they thought expired at a different time. However, when the healthcare provider entered the lot number on Moderna's online expiration tool look up, it was found that the lot had expired on 02-Apr-2022. The healthcare provider reported that each patient was administered with a dose from a different vial and each of the vial was stored in the refrigerator on the day before administration. The vial did not undergo any temperature excursion. It was reported that the patient had not reported of experiencing any adverse reactions to this expired dose. Treatment information was not provided. Most recent FOLLOW-UP information incorporated above includes: On 04-May-2022: Significant follow up contains : Added reporter, updated suspect product dose details, and updated narrative. On 05-May-2022: Follow-up received and reporter's email address updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268744

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 70,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268740

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 63,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268736

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 70,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268730

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 80,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268727

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268723

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268720

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 26,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268718

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 76,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268712

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 73,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268709

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 81,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268706

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 75,0
Geschlecht: F
Eingang: 10.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268702

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 76,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268496

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 25,0
Geschlecht: M
Eingang: 10.05.2022
Impfdatum: 05.04.2022
Beginn: 05.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Expired vial was stored in the refrigerator the day before administration; expired dose administered to patient; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired dose administered to patient) and PRODUCT STORAGE ERROR (Expired vial was stored in the refrigerator the day before administration) in a 25-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 05-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 05-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expired dose administered to patient). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Expired vial was stored in the refrigerator the day before administration). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expired dose administered to patient) and PRODUCT STORAGE ERROR (Expired vial was stored in the refrigerator the day before administration) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No information on concomitant medication was reported. It was reported that, the vials was initially stored in refrigerator a day before the administration and vials did not undergo any temperature excursions. The patient had not reported any adverse reactions to this dose. No information on treatment medications was reported. Most recent FOLLOW-UP information incorporated above includes: On 05-May-2022: Follow-up information received contains no new information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267676

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 20,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267673

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 66,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267662

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 61,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267661

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 57,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267654

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 57,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267652

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 69,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267645

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 72,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267640

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 65,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267636

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 72,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267634

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 60,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267598

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 65,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267581

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 63,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267576

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 73,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267573

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 76,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267564

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 23,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267555

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267553

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 65,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267545

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 39,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267538

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 66,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267535

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 81,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267529

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 72,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/06/2022, vaccine was given on 04/06/2022. Moderna was contacted once we were made aware that the vaccine had expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2267518

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 62,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered

Symptomtext

Vaccine expired on 04/02/2022, vaccine was given on 04/06/22. Moderna was contacted when we were made aware that the vaccine was expired. Moderna concluded that the vaccine had maintained viability and no reimmunization was needed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2263957

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 29,0
Geschlecht: M
Eingang: 04.05.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered No adverse event

Symptomtext

Moderna COVID-19 vaccine EUA. Patient received COVID-19 vaccine booster dose on 4/6/2022. No symptoms or adverse events noted during administration and observation. No adverse events reported by the patient to date. On 5/4/2022, discovered the dose administered is past expiration or beyond-use date. Manufacturer contacted to report event and to obtain revaccination guidance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2263956

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 23,0
Geschlecht: M
Eingang: 04.05.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered No adverse event

Symptomtext

Moderna COVID?19 Vaccine EUA Patient received COVID-19 vaccine booster dose on 4/4/2022. No symptoms or adverse events noted during administration and observation. No adverse events reported by the patient to date. On 5/4/2022 discovered that dose administered is past the expiration or beyond-use date. Manufacturer contacted to report event and to obtain re-vaccination guidance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2263955

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 25,0
Geschlecht: M
Eingang: 04.05.2022
Impfdatum: 05.04.2022
Beginn: 05.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered No adverse event

Symptomtext

Moderna COVID?19 Vaccine EUA Patient received COVID-19 vaccine booster dose on 4/6/2022. No symptoms or adverse events noted during administration and observation. No adverse events reported by the patient to date. On 5/4/2022 discovered that dose administered is past the expiration or beyond-use date. Manufacturer contacted to report event and to obtain re-vaccination guidance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2263954

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 20,0
Geschlecht: M
Eingang: 04.05.2022
Impfdatum: 07.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Expired product administered No adverse event

Symptomtext

Moderna COVID?19 Vaccine EUA Patient received COVID-19 vaccine booster dose on 4/7/2022. No symptoms or adverse events noted during administration and observation. No adverse events reported by the patient to date. On 5/4/2022 discovered that dose administered is past the expiration or beyond-use date. Manufacturer contacted to report event and to obtain re-vaccination guidance.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: PCN (hives)
Vorherige Impfungen: -

VAERS 2254530

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 04.06.2021
Beginn: 09.04.2022
Tage bis Beginn: 309,0
Dosis: 2
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: unbekannt Erholt: unbekannt

COVID-19 Chest discomfort Cough SARS-CoV-2 test positive

Symptomtext

4/9/22 PMH of depression, and anxiety present to the ED with c/o left sided chest tightness/cough worsening over the past week.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 4/9/22 SARS-CoV-2 (COVID-19) by NAA-- Detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2252341

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

gering

Staat: TN
Alter: 8,0
Geschlecht: M
Eingang: 26.04.2022
Impfdatum: 25.04.2022
Beginn: 25.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Product administered to patient of inappropriate age

Symptomtext

There are no symptoms. A child received a Moderna shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2252332

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

gering

Staat: TN
Alter: 9,0
Geschlecht: M
Eingang: 26.04.2022
Impfdatum: 25.04.2022
Beginn: 25.04.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

No adverse event Product administered to patient of inappropriate age

Symptomtext

There were no symptoms. The child received a Moderna vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2245567

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MD
Alter: 32,0
Geschlecht: F
Eingang: 21.04.2022
Impfdatum: 22.03.2022
Beginn: 14.04.2022
Tage bis Beginn: 23,0
Dosis: 1
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Inappropriate schedule of product administration

Symptomtext

Patient received a second shot earlier than normal; This spontaneous case was reported by a medical assistant and describes the occurrence of INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received a second shot earlier than normal) in a 32-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 033K21-2A and 068H21A) for COVID-19 vaccination. Patient had no past medical history. On 22-Mar-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 14-Apr-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 14-Apr-2022, after starting mRNA-1273 (Spikevax), the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received a second shot earlier than normal). At the time of the report, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Patient received a second shot earlier than normal) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. Patient had no side effects. No treatment information was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no past medical history.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2243785

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

gering

Staat: WI
Alter: 29,0
Geschlecht: F
Eingang: 20.04.2022
Impfdatum: 08.01.2022
Beginn: 02.02.2022
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Abortion spontaneous Blood test abnormal Exposure during pregnancy Pregnancy Pregnancy test positive Ultrasound antenatal screen abnormal

Symptomtext

Positive pregnancy test on 1/15, received covid booster 1/8 and confirmed missed miscarriage on 2/22/2020. No previous history/family history of miscarriage

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abortion spontaneous
Hospital-Tage: -
Labordaten: Multiple Ultrasounds and bloodwork
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Sertraline
Allergien: -
Vorherige Impfungen: -

VAERS 2240457

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 67,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 13.04.2022
Beginn: 13.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vial initially stored in the refrigerator on 14 Mar 2022, manufacturer date of expiry was on 02 Apr 2022; Expired dose administered; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered) and PRODUCT STORAGE ERROR (Vial initially stored in the refrigerator on 14 Mar 2022, manufacturer date of expiry was on 02 Apr 2022) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 13-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial initially stored in the refrigerator on 14 Mar 2022, manufacturer date of expiry was on 02 Apr 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered) and PRODUCT STORAGE ERROR (Vial initially stored in the refrigerator on 14 Mar 2022, manufacturer date of expiry was on 02 Apr 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication reported. The vial was initially stored in the refrigerator on 14 Mar 2022. Expiration date of the vial was on 02 Apr 2022. The vial did not undergo any temperature excursions. No treatment medication details reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2240456

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 73,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 13.04.2022
Beginn: 06.04.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Accidental underdose Expired product administered Product storage error

Symptomtext

Dose administered after 30-day Use By Date or after manufacturer date of expiry; Expired dose administered to 5 patients; 0.25ML/3rd dose; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 5 patients), ACCIDENTAL UNDERDOSE (0.25ML/3rd dose) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) in a 73-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 5 patients) and ACCIDENTAL UNDERDOSE (0.25ML/3rd dose). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry). On 06-Apr-2022, EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 5 patients) outcome was unknown. At the time of the report, ACCIDENTAL UNDERDOSE (0.25ML/3rd dose) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) outcome was unknown. 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: 14-Mar-2022. The vial did not undergo any temperature excursions. No concomitant medications was reported. No treatment medications was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Accidental underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2240455

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 71,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 13.04.2022
Beginn: 13.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

5 patients were vaccinated on 13 Apr 2022,expiration date was on 02 Apr 2022; Expired dose administered to 5 patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 5 patients) and PRODUCT STORAGE ERROR (5 patients were vaccinated on 13 Apr 2022,expiration date was on 02 Apr 2022) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 13-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 5 patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (5 patients were vaccinated on 13 Apr 2022,expiration date was on 02 Apr 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 5 patients) and PRODUCT STORAGE ERROR (5 patients were vaccinated on 13 Apr 2022,expiration date was on 02 Apr 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The vial was initially stored in the refrigerator on 14-Mar-2022. No treatment information was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2240454

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 72,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 13.04.2022
Beginn: 13.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered

Symptomtext

This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered) in a 72-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 13-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered). On 13-Apr-2022, EXPIRED PRODUCT ADMINISTERED (Expired dose administered) 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.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2240453

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 61,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) in a 62-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. The vial was initially stored in the refrigerator on 14-Mar-2022. The vial did not undergo any temperature excursions. No concomitant medication reported. No treatment medication details reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2240451

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 59,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Circumstance or information capable of leading to medication error Expired product administered Product storage error

Symptomtext

Dose administered after 30-day Use By Date or after manufacturer date of expiry; 0.25ML/3rd dose; Expired dose administered to 14 patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients), PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) and CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (0.25ML/3rd dose) in a 60-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) and CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (0.25ML/3rd dose). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients), PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) and CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (0.25ML/3rd dose) outcome was unknown. 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: 14-Mar-2022. The vial did not undergo any temperature excursions. No concomitant medications was reported. No treatment medications was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Circumstance or information capable of leading to medication error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2240450

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 87,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

14 patients were vaccinated on 06Apr2022,Expiration date: 02Apr2022; Expired dose administered to 14 patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) and PRODUCT STORAGE ERROR (14 patients were vaccinated on 06Apr2022,Expiration date: 02Apr2022) in an 88-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (14 patients were vaccinated on 06Apr2022,Expiration date: 02Apr2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) and PRODUCT STORAGE ERROR (14 patients were vaccinated on 06Apr2022,Expiration date: 02Apr2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Date the vial was initially stored in the refrigerator was on 14-MAR-2022. No treatment information was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2240449

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 67,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Circumstance or information capable of leading to medication error Expired product administered

Symptomtext

Expired dose administered; 0.25Ml/3rd Dose; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered) and CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (0.25Ml/3rd Dose) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered) and CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (0.25Ml/3rd Dose). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered) and CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (0.25Ml/3rd Dose) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The vial was initially stored in the refrigerator on 14-Mar-2022. The vial did not undergo any temperature excursions. No treatment medication was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Circumstance or information capable of leading to medication error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2240448

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 50,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Expired dose administered to 14 patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication list was not provided. The vial was initially stored in the refrigerator on 14-Mar-2022. The vial did not undergo 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: -

VAERS 2240443

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 53,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Expired dose administered; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered) in a 53-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The vial was initially stored in the refrigerator on 14-Mar-2022. The vial did not undergo any temperature excursions. No treatment medication was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2240442

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 65,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Expired Vaccine administered; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered) in a 66-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The vial was initially stored in the refrigerator on 14-Mar-2022. The vial did not undergo any temperature excursions. No concomitant medication reported. No treatment medication details reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2240439

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 69,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Dose administered after 30-day Use By Date or after manufacturer date of expiry; Expired dose administered to patient; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered to patient) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) in a 69-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) .5 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered to patient). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered to patient) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Date the vial was initially stored in the refrigerator :14 Mar 2022. Vial did not undergo any temperature excursion. No concomitant medication 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: -

VAERS 2240438

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 61,0
Geschlecht: M
Eingang: 19.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered) and PRODUCT STORAGE ERROR (14 patients were vaccinated on 06Apr2022, vaccine Expiration date: 02Apr2022) in a 61-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (14 patients were vaccinated on 06Apr2022, vaccine Expiration date: 02Apr2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered) and PRODUCT STORAGE ERROR (14 patients were vaccinated on 06Apr2022, vaccine Expiration date: 02Apr2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. Treatment information was not reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2238356

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 77,0
Geschlecht: M
Eingang: 18.04.2022
Impfdatum: 13.04.2022
Beginn: 13.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Expired dose administered; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered) in a 75-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 13-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. The vial was initially stored in the refrigerator on 14 Mar 2022. The vial did not undergo any temperature excursions. Treatment information was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2238349

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 64,0
Geschlecht: M
Eingang: 18.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Expired dose administered to 14 patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) in a 65-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The vial was initially stored in the refrigerator on 14 Mar 2022. No treatment information was reported. This case was linked to MOD-2022-539669 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2238290

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 87,0
Geschlecht: M
Eingang: 18.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Dose administered after 30-day Use By Date or after manufacturer date of expiry; Expired dose administered to 14 patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) in an 88-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The vial was initially stored in the refrigerator on 14-Mar-2022 The vial did not undergo any temperature excursions. No concomitant medication reported. No treatment medication details reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2238289

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 83,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Expired dose administered to 14 patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) in an 84-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. Date the vial was initially stored in the refrigerator: 14-Mar-2022 the vial did not undergo any temperature excursions. No treatment medications was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2238288

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 71,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Expired dose administered; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. Treatment information was unknown.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2238286

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: IL
Alter: 38,0
Geschlecht: M
Eingang: 18.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Circumstance or information capable of leading to medication error Expired product administered Product storage error

Symptomtext

Dose administered after 30-day Use By Date or after manufacturer date of expiry; Expired dose administered to 14 patients; 0.25ml/3rd; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients), CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (0.25ml/3rd) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) in a 39-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients) and CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (0.25ml/3rd). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired dose administered to 14 patients), CIRCUMSTANCE OR INFORMATION CAPABLE OF LEADING TO MEDICATION ERROR (0.25ml/3rd) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date or after manufacturer date of expiry) outcome was unknown. 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: 14-Mar-2022 The vial does not undergo any temperature excursions. No concomitant medications was reported. No treatment medications was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Circumstance or information capable of leading to medication error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2237405

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

gering

Staat: CA
Alter: 47,0
Geschlecht: M
Eingang: 16.04.2022
Impfdatum: 07.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

The vial was initially stored in the refrigerator on 14-Mar-2022 and administration of expired vaccine on 07-April-2022; received expired dose; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received expired dose) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 14-Mar-2022 and administration of expired vaccine on 07-April-2022) in a 47-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 068h21a) for COVID-19 vaccination. No Medical History information was reported. On 07-Apr-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 07-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (received expired dose). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 14-Mar-2022 and administration of expired vaccine on 07-April-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (received expired dose) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 14-Mar-2022 and administration of expired vaccine on 07-April-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported The vial was initially stored in the refrigerator on 14-Mar-2022. No temperature excursion. No treatment drugs were reported. This case was linked to MOD-2022-535994 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 08-Apr-2022: Follow-up received included reporter correct name and date of initially stored in the refrigerator updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2237403

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

gering

Staat: CA
Alter: 45,0
Geschlecht: M
Eingang: 16.04.2022
Impfdatum: 07.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

received expired doses; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received expired doses) in a 45-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 068h21a) for COVID-19 vaccination. No Medical History information was reported. On 07-Apr-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 07-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (received expired doses). At the time of the report, EXPIRED PRODUCT ADMINISTERED (received expired doses) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. The vial was initially stored in the refrigerator on 14-Mar-2022. No concomitant medications were reported No treatment medications were reported This case was linked to MOD-2022-536011 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 08-Apr-2022: Live Follow up received contained Significant information reporter correct name was provided and date the vial was initially stored in the refrigerator was reported and narrative updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2237372

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CT
Alter: -
Geschlecht: M
Eingang: 16.04.2022
Impfdatum: 07.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Patient recived expired Moderna Covid-19 vaccine; Patient recived expired Moderna Covid-19 vaccine; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (Patient recived expired Moderna Covid-19 vaccine) and EXPIRED PRODUCT ADMINISTERED (Patient recived expired Moderna Covid-19 vaccine) in an 81-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 07-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 07-Apr-2022, the patient experienced PRODUCT STORAGE ERROR (Patient recived expired Moderna Covid-19 vaccine) and EXPIRED PRODUCT ADMINISTERED (Patient recived expired Moderna Covid-19 vaccine). At the time of the report, PRODUCT STORAGE ERROR (Patient recived expired Moderna Covid-19 vaccine) and EXPIRED PRODUCT ADMINISTERED (Patient recived expired Moderna Covid-19 vaccine) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No relevant concomitant medications were reported. Treatment information was unknown. Date the vial was initially stored in the refrigerator: 31-Mar-2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2237364

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 16.04.2022
Impfdatum: 07.04.2022
Beginn: 07.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Patient received expired vaccine on 07-Apr-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received expired vaccine on 07-Apr-2022) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 07-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received expired vaccine on 07-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received expired vaccine on 07-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Vial did not undergo any temperature excursions. Vial was initially stored in refrigerator on 07-Apr-2022. patient was given vaccine that Expired on Second. No concomitant medications was provided by the reporter. No treatment medications was provided by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 07-Apr-2022: Follow-up received contain non significant information

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2225183

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: -
Geschlecht: M
Eingang: 09.04.2022
Impfdatum: 06.04.2022
Beginn: 06.04.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Patient was administered with an expired vaccine; This spontaneous case was reported by a consumer and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered with an expired vaccine) in a male patient of an unknown age who received mRNA-1273 (Spikevax) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered with an expired vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient was administered with an expired vaccine) outcome was unknown. No concomitant medication were reported. No treatment drug were reported. Most recent FOLLOW-UP information incorporated above includes: On 06-Apr-2022: Follow up document contain no new information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2223208

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

gering

Staat: CA
Alter: 42,0
Geschlecht: F
Eingang: 08.04.2022
Impfdatum: 04.04.2022
Beginn: 01.04.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered No adverse event

Symptomtext

No adverse effect. Patient received expired vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2220166

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MN
Alter: 49,0
Geschlecht: M
Eingang: 07.04.2022
Impfdatum: 31.01.2022
Beginn: 06.04.2022
Tage bis Beginn: 65,0
Dosis: 3
Route/Site: UN / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

COVID-19 SARS-CoV-2 test positive

Symptomtext

Patient vaccinated against and then tested positive for COVID19

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2219761

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 57,0
Geschlecht: M
Eingang: 07.04.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Given an expired dose of the Moderna COVID19 vaccine; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Given an expired dose of the Moderna COVID19 vaccine) in a 57-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 04-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Given an expired dose of the Moderna COVID19 vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Given an expired dose of the Moderna COVID19 vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information provided. No treatment medication information provided. Dose was administered after 30-day Use By Date or after manufacturer date of expiry. Date the vial was initially stored in the refrigerator was reported as 16 Mar 2022. The vial did not undergo any temperature excursions. Most recent FOLLOW-UP information incorporated above includes: On 04-Apr-2022: Follow up received contains significant information Patient details were added. On 04-Apr-2022: Follow up received contains no new information

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2217814

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: OH
Alter: -
Geschlecht: M
Eingang: 06.04.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Patient received a booster dose of the Moderna Covid 19 vaccine that was expired on 02Apr2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received a booster dose of the Moderna Covid 19 vaccine that was expired on 02Apr2022) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 04-Apr-2022 at 7:00 AM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Apr-2022 at 7:00 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received a booster dose of the Moderna Covid 19 vaccine that was expired on 02Apr2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received a booster dose of the Moderna Covid 19 vaccine that was expired on 02Apr2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. It was reported that patient received a booster dose. This vial was stored in the freezer until this morning (04Apr2022) at 6AM. Vial did not undergo any temperature excursions. No treatment medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2215897

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 66,0
Geschlecht: M
Eingang: 05.04.2022
Impfdatum: 04.04.2022
Beginn: 04.04.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Product storage error

Symptomtext

Moderna lot # 068H21A exp. 04/02/22 was given to pt. on 04/04/22. Notified Moderna 866-663-3762. Awaiting response.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2213657

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 65,0
Geschlecht: M
Eingang: 03.04.2022
Impfdatum: 03.01.2022
Beginn: 07.01.2022
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: ja Disable: unbekannt ER: ja Erholt: nein

Asthenia COVID-19 Rhabdomyolysis SARS-CoV-2 test positive

Symptomtext

Narrative: The patient received one dose of Moderna COVID 19 Vaccine on 3 Jan 2022. The patient tested positive for COVID 19 on 7 Jan 22. The patient presented to the ED with weakness and rhabdomyolysis. The patient was admitted to the hospital and treated with fluids and statin on hold. The patient was discharged on 8 Jan 2022 in stable condition.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Asthenia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2206657

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

gering

Staat: -
Alter: 55,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 28.01.2022
Beginn: 30.03.2022
Tage bis Beginn: 61,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

No adverse event Underdose

Symptomtext

Patient has reported no adverse effects. Upon entering information into the vaccine registry is when the error was noticed. Patient received booster dose instead of full second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2206654

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

gering

Staat: -
Alter: 17,0
Geschlecht: M
Eingang: 30.03.2022
Impfdatum: 07.01.2022
Beginn: 30.03.2022
Tage bis Beginn: 82,0
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

Patient has reported no symptoms. Upon entering information to vaccine registry is when the error was noticed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2204698

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 26,0
Geschlecht: F
Eingang: 29.03.2022
Impfdatum: 26.03.2022
Beginn: 26.03.2022
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Incorrect dose administered

Symptomtext

At approximately 10:32 AM, client arrived to vaccine site and requested a second Moderna vaccine. Per Nurse, client stated, "I'm here for my second Moderna dose". Nurse proceeded to administer second Moderna vaccine (left arm, LOT # 068H21A, Expires 4/2/22, at approximately 10:32 AM on 03/26/2022 and verified client's COVID-19 vaccine card which displayed one first Moderna on 04/20/2021. At approximately 2:45 pm, staff member reported to Lead Nurse and Nurse that client's record displayed 2 doses of Moderna vaccine (04/20/2021 and 12/31/2021) and staff stated that client "needed Moderna booster, not a second Moderna dose". Nurse called client twice to attempt to clarify client's vaccination record. Nurse left 2 messages with a return phone number on 3/26/22 and 3/29/22). No response from client. No further details left on client's voicemail.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Incorrect dose administered
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: at approximately 10:32 AM on 03/26/2022.
Vorgeschichte: at approximately 10:32 AM on 03/26/2022.
Andere Medikamente: None reported
Allergien: none reported
Vorherige Impfungen: -

VAERS 2200409

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: GA
Alter: 34,0
Geschlecht: U
Eingang: 26.03.2022
Impfdatum: 15.02.2022
Beginn: 21.03.2022
Tage bis Beginn: 34,0
Dosis: 1
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccine administered after the 30-day beyond use date of 18-Mar-2022; patient received expired dose; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient received expired dose) and PRODUCT STORAGE ERROR (Vaccine administered after the 30-day beyond use date of 18-Mar-2022) in a 34-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch nos. 012H21B and 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Feb-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 21-Mar-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 21-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient received expired dose). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine administered after the 30-day beyond use date of 18-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient received expired dose) and PRODUCT STORAGE ERROR (Vaccine administered after the 30-day beyond use date of 18-Mar-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment information was reported. On 24-Feb-2022, the vaccine was moved from the freezer to the refrigerator. On 21-Mar-2022, at 04:00 P.M., the vaccine vial was opened. This case was linked to MOD-2022-520795 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2199179

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 38,0
Geschlecht: M
Eingang: 25.03.2022
Impfdatum: 24.03.2022
Beginn: 24.03.2022
Tage bis Beginn: 0,0
Dosis: 5
Route/Site: IM / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Extra dose administered Interchange of vaccine products

Symptomtext

Patient currently asymptomatic. No adverse events regarding vaccination administration error. Patient initially received Moderna two-dose series on 1/12/2021 and 2/10/2021 at a different facility. Patient then transferred from that facility whereupon he received Pfizer series on 8/5/2021 and 9/8/2021. Patient then transferred to our facility and received a Moderna booster dose on 3/24/2022. Staff were unaware of the initial Moderna series administered; therefore administered the Moderna booster dose based on the Pfizer series completion dates previously provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: N/A.
Vorgeschichte: Asthma, constipation, hypertension, hypothyroidism, dysphagia, vitamin D deficiency, and allergic rhinitis.
Andere Medikamente: Xopenex PRN, Sennoside, Amitiza, Polyethylene glycol, Lactulose (PRN), Omeprazole, Antacid PRN, MI (PRN), Hydrochlorothiazide, Metoprolol, Levothyroxine sodium, Acetaminophen (PRN), Gemfibrozil, Vitamin D3 and Metformin.
Allergien: NKA.
Vorherige Impfungen: -

VAERS 2198207

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: GA
Alter: 33,0
Geschlecht: U
Eingang: 25.03.2022
Impfdatum: 15.02.2022
Beginn: 21.03.2022
Tage bis Beginn: 34,0
Dosis: 1
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

The 30-day beyond use date was 18Mar2022; patients received expired doses; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patients received expired doses) and PRODUCT STORAGE ERROR (The 30-day beyond use date was 18Mar2022) in a 33-year-old patient of an unknown gender who received mRNA-1273 (Spikevax) (batch nos. 012H21B and 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Feb-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 21-Mar-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 21-Mar-2022, after starting mRNA-1273 (Spikevax), the patient experienced EXPIRED PRODUCT ADMINISTERED (patients received expired doses). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The 30-day beyond use date was 18Mar2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patients received expired doses) and PRODUCT STORAGE ERROR (The 30-day beyond use date was 18Mar2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The vials were moved from freezer to refrigerated condition on 24 Feb 2022. The vaccine vial was opened on 21 Mar 2022 at 4:00 pm. No treatment medication was reported. This case was linked to MOD-2022-521064 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 23-Mar-2022: Significant follow up was received and patient demographics, suspect information were updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2196307

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068h21a

gering

Staat: MA
Alter: 72,0
Geschlecht: M
Eingang: 24.03.2022
Impfdatum: 23.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Inappropriate schedule of product administration

Symptomtext

Patient received two Moderna booster dose one month apart by mistake. He had received Moderna primary series and a booster dose and was up to date with COVID 19 vaccines. While admitted in the hospital they were ordered for a booster dose when in fact they were up to date and did not need any additional doses.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: none
Vorherige Impfungen: -

VAERS 2195180

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 43,0
Geschlecht: M
Eingang: 23.03.2022
Impfdatum: 23.03.2022
Beginn: 23.03.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: unbekannt

Underdose

Symptomtext

Patient was supposed to get moderna first dose but instead received moderna booster dose (0.25mL)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Underdose
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2189946

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: ME
Alter: 61,0
Geschlecht: M
Eingang: 21.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 4
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Extra dose administered

Symptomtext

The staff made appt, received consent from the POA, presented a card with 2 doses, upon entry to IMMPACT a dose has previously been administered on 11/7/2021. This was confirmed had administered but staff at the facility did not record.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Extra dose administered
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none know
Vorgeschichte: in a residential facility
Andere Medikamente: not reported
Allergien: IBU
Vorherige Impfungen: -

VAERS 2189289

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: CA
Alter: 45,0
Geschlecht: M
Eingang: 20.03.2022
Impfdatum: 02.03.2022
Beginn: 02.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Vitiligo

Symptomtext

Expression of vitiligo in hands, armpit and groin.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vitiligo
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2187103

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 22,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 09.02.2022
Beginn: 11.03.2022
Tage bis Beginn: 30,0
Dosis: 1
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vial was punctured on 10-Mar-2022 at 9:24 and refrigerated post 12 hours puncture; Dose was given past 12 hour post-puncture; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose was given past 12 hour post-puncture) and PRODUCT STORAGE ERROR (Vial was punctured on 10-Mar-2022 at 9:24 and refrigerated post 12 hours puncture) in a 22-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 033K21-2A and 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 09-Feb-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 11-Mar-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 11-Mar-2022, after starting mRNA-1273 (Spikevax), the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose was given past 12 hour post-puncture). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was punctured on 10-Mar-2022 at 9:24 and refrigerated post 12 hours puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose was given past 12 hour post-puncture) and PRODUCT STORAGE ERROR (Vial was punctured on 10-Mar-2022 at 9:24 and refrigerated post 12 hours puncture) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Vial was initially stored in the refrigerator on 10-Mar-2022. Vial was punctured on 10-Mar-2022 at 9:24 and stored in fridge post puncture. Vial did not undergo any temperature excursion. For a very minimal time vial was exposed to room temperature (8 to 25 degree Celsius) 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: -

VAERS 2187102

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 60,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 11.02.2022
Beginn: 11.03.2022
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Dose given more that 12 hour post puncture; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose given more that 12 hour post puncture) in a 60-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 033K21-2A and 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Feb-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 11-Mar-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 11-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose given more that 12 hour post puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose given more that 12 hour post puncture) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. Reporter stated that the vial was initially stored in the refrigerator on 10-Mar-2022 and was first punctured on the same day of 10-Mar-2022 at 9:24 AM. The vial was then stored in the fridge after puncturing and the vial did not undergo any temperature excursions. The total amount of time the vial was exposed to room temperature range was very minimal (only taken out to draw the doses). No treatment medications were provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2187100

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 11.02.2022
Beginn: 11.03.2022
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Dose given more than 12 hour post-puncture; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose given more than 12 hour post-puncture) in a 51-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 033K21-2A and 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Feb-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 11-Mar-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 11-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose given more than 12 hour post-puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose given more than 12 hour post-puncture) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. It was reported that the vaccine was punctured on thursday morning 10-Mar-2022 at 9:24 AM. Date the vial was initially stored in the refrigerator was 10-Mar-2022 and the vial did not undergo any temperature excursions. Amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) was very minimal (only taken out to draw the doses). No treatment medication were provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2187099

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NY
Alter: 18,0
Geschlecht: M
Eingang: 18.03.2022
Impfdatum: 11.02.2022
Beginn: 11.03.2022
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Dose given more than 12 hour post-puncture; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose given more than 12 hour post-puncture) in an 18-year-old male patient who received mRNA-1273 (Spikevax) (batch nos. 033K21-2A and 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Feb-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 11-Mar-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 11-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose given more than 12 hour post-puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose given more than 12 hour post-puncture) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. It was reported that the vaccine was punctured on thursday morning 10-Mar-2022 at 9:24 AM. Date the vial was initially stored in the refrigerator was 10-Mar-2022 and the vial did not undergo any temperature excursions. Amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) was very minimal (only taken out to draw the doses). No treatment medication were provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2184294

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: VT
Alter: 65,0
Geschlecht: F
Eingang: 17.03.2022
Impfdatum: 15.03.2022
Beginn: 15.03.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Inappropriate schedule of product administration

Symptomtext

Patient came in to clinic to receive her booster. Vaccinator administered the booster dose without checking the prior vaccination date on the card. Patient's dose 2 vaccine was on 12/29/21 and she was not supposed to receive her booster vaccine until May 2022, so she received it two months early. Staff monitored the patient for a full 30 minutes to ensure no adverse reaction and patient tolerated the dose well. Both prior vaccinations were also Moderna.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Eggs
Vorherige Impfungen: Flu vaccine

VAERS 2168237

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: KY
Alter: 13,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 25.01.2022
Beginn: 25.01.2022
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: - / UN

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

No adverse event Product administered to patient of inappropriate age

Symptomtext

Patient is under 18 years of age and was given the 1st dose Moderna Vaccine. Patient has no AE at this time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Migraines, asthma, anxiety and depression, allergies, GERD
Andere Medikamente: singular, Zyrtec D, Prilosec, maxalt, Topamax, viennva, Trenpion ointment, buspirone, Prozac,
Allergien: nka
Vorherige Impfungen: -

VAERS 2137262

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccines placed in refrigerator on 13 Jan 2022 and dose administered on 17 Feb 2022; patient received expired doses of the Moderna COVID vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13 Jan 2022 and dose administered on 17 Feb 2022) in a 67-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient received expired doses of the Moderna COVID vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13 Jan 2022 and dose administered on 17 Feb 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13 Jan 2022 and dose administered on 17 Feb 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant Drug details were reported. No Treatment information was provided. This case was linked to MOD-2022-491752 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137262

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 67,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccines placed in refrigerator on 13 Jan 2022 and dose administered on 17 Feb 2022; patient received expired doses of the Moderna COVID vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patient received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13 Jan 2022 and dose administered on 17 Feb 2022) in a 67-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patient received expired doses of the Moderna COVID vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13 Jan 2022 and dose administered on 17 Feb 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patient received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13 Jan 2022 and dose administered on 17 Feb 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant Drug details were reported. No Treatment information was provided. This case was linked to MOD-2022-491752 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137253

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 28,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

received expired doses of the Moderna COVID vaccine; Vaccines placed in refrigerator on 13-Jan-2022 and dose administered to patient on 17-Feb-2022; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13-Jan-2022 and dose administered to patient on 17-Feb-2022) in a 28-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13-Jan-2022 and dose administered to patient on 17-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13-Jan-2022 and dose administered to patient on 17-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 reported by the reporter. The vaccines were placed in refrigerator on 13-Jan-2022. Expiration date placed on vial was 12-Feb-2022. No treatment medication was reported by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137253

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 28,0
Geschlecht: F
Eingang: 05.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

received expired doses of the Moderna COVID vaccine; Vaccines placed in refrigerator on 13-Jan-2022 and dose administered to patient on 17-Feb-2022; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13-Jan-2022 and dose administered to patient on 17-Feb-2022) in a 28-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13-Jan-2022 and dose administered to patient on 17-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13-Jan-2022 and dose administered to patient on 17-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 reported by the reporter. The vaccines were placed in refrigerator on 13-Jan-2022. Expiration date placed on vial was 12-Feb-2022. No treatment medication was reported by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137214

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: -
Alter: 51,0
Geschlecht: M
Eingang: 05.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Vaccines placed in refrigerator on 13-Jan-2022 and dose admistered to patient on 17-Feb-2022; patients who received expired doses of the Moderna COVID vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13-Jan-2022 and dose admistered to patient on 17-Feb-2022) in a 51-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13-Jan-2022 and dose admistered to patient on 17-Feb-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 13-Jan-2022 and dose admistered to patient on 17-Feb-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that the vaccines were placed in refrigerator on 13-Jan-2022. Expiration date placed on vial was12-Feb-2022. No concomitant medication was reported by the reporter. No treatment medication was reported by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2151824

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: NC
Alter: 67,0
Geschlecht: F
Eingang: 02.03.2022
Impfdatum: 25.01.2021
Beginn: 29.01.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: SYR / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Joint stiffness Swelling

Symptomtext

Extreme joint stiffness and it continues today (almost 2 years later). Initially, I could barely get out of bed or stand up straight when getting out of a chair. It has lessened but not gone away completely. I'll take anti-inflammatory to help. I can be driving my car and my elbows will start aching. I can sit for awhile and then my hips will ache. On occasion, my eyeballs will swell. I have always been very energetic and basically a "tom-girl"; since having the vaccines, I am stiff and lacking flexibility.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Joint stiffness
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Sulfa drugs
Vorherige Impfungen: Flu about age 28, 1983.

VAERS 2151164

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: FL
Alter: 52,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 02.02.2022
Beginn: 03.02.2022
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Peripheral swelling Swollen tongue Throat irritation

Symptomtext

Patient called the day after her vaccination and stated that she had a reaction to the vaccine. The symptoms started within 24 hours of getting the vaccine. The symptoms included itchy throat, swelling in her tongue, swelling in her entire right arm that last 2 weeks. She stated she was taking advil and an antihistamine the entire time.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Peripheral swelling
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2150663

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 48,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Received expired doses of the Moderna COVID vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired doses of the Moderna COVID vaccine) in a 48-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired doses of the Moderna COVID vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received expired doses of the Moderna COVID vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported. On 13-Jan-2022, the vial was initially stored in the refrigerator. It was reported that as per the healthcare provider, the vials were set to expire on 12-Feb-2022 based on the stickers put on them. The healthcare provider was not sure and did not have the exact expiration date of the vial itself. The healthcare provider asked if they are going to revaccinate the patient or not.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2150661

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

patients who received expired doses of the Moderna COVID vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine) in a 67-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. On 13-Jan-2022, Vaccines placed in refrigerator. No treatment information was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2150660

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 60,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 13.01.2022
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Patients who received expired doses of the Moderna COVID vaccine; Vaccines placed in refrigerator on 1/13/2022 and dose administered to patient on 2/17/2022; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients who received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 1/13/2022 and dose administered to patient on 2/17/2022) in a 60-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Jan-2022, the patient experienced PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 1/13/2022 and dose administered to patient on 2/17/2022). On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients who received expired doses of the Moderna COVID vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients who received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator on 1/13/2022 and dose administered to patient on 2/17/2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported. This case was linked to MOD-2022-491752 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2150658

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 58,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

This spontaneous case reported by a pharmacist, describes the occurrence of administered expired product (patient received expired dose of the Moderna COVID-19 vaccine) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 vaccine, batch/lot# 068H21A) for COVID-19 immunization. No medical history reported. On Feb 17, 2022, patient received the third dose of mRNA-1273 (Moderna COVID-19 vaccine), unknown route; 1 dosage form. On Feb 17, 2022, patient administered expired product (patient received expired dose of the Moderna COVID-19 vaccine). At the time of the report, administered expired product (patient received expired dose of the Moderna COVID-19 vaccine) outcome: unknown. The vaccine placed in refrigerator on Jan 13, 2022. The reporter did not provide any causality assessments, concomitant medication or treatment information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2150649

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 43,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 01.02.2022
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Received expired doses of the Moderna COVID vaccine; Vaccines placed in refrigerator was on 13 Jan 2022 but doses were administered to patient on 17 Feb 2022; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator was on 13 Jan 2022 but doses were administered to patient on 17 Feb 2022) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In February 2022, the patient experienced PRODUCT STORAGE ERROR (Vaccines placed in refrigerator was on 13 Jan 2022 but doses were administered to patient on 17 Feb 2022). On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired doses of the Moderna COVID vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Vaccines placed in refrigerator was on 13 Jan 2022 but doses were administered to patient on 17 Feb 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. It was reported that the vaccines placed in refrigerator was on 13 Jan 2022, expiration date placed on vial was on 12 Feb 2022 and doses administered to patient on 17 Feb 2022. No treatment information was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2150389

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 30,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: ja

Expired product administered Maternal exposure during breast feeding

Symptomtext

Pharmacist called, they administered 2 expired vaccines/administration of an expired vaccine; Maternal Exposure during breastfeeding; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Pharmacist called, they administered 2 expired vaccines/administration of an expired vaccine) and MATERNAL EXPOSURE DURING BREAST FEEDING (Maternal Exposure during breastfeeding) in a 30-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Pharmacist called, they administered 2 expired vaccines/administration of an expired vaccine) and MATERNAL EXPOSURE DURING BREAST FEEDING (Maternal Exposure during breastfeeding). On 17-Feb-2022, MATERNAL EXPOSURE DURING BREAST FEEDING (Maternal Exposure during breastfeeding) had resolved. At the time of the report, EXPIRED PRODUCT ADMINISTERED (Pharmacist called, they administered 2 expired vaccines/administration of an expired vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. No treatment medications were provided. Vaccines placed in refrigerator on 13-Jan-2022 This case was linked to MOD-2022-491348 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 24-Feb-2022: Follow-up received on 24-FEB-2022, contains patient details. On 25-Feb-2022: Follow-up document received on 25-FEB-2022, contains no new information.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137363

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 36,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

patients who received expired doses of the Moderna COVID vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine) in a 36-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Vaccines were placed in refrigerator On 13-Jan-2022. The treatment information was unknown. This case was linked to MOD-2022-491752 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137363

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 36,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

patients who received expired doses of the Moderna COVID vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine) in a 36-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Vaccines were placed in refrigerator On 13-Jan-2022. The treatment information was unknown. This case was linked to MOD-2022-491752 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137356

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 59,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Dose administered after 30-day Use By Date; Dose administered after 30-day Use By Date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant and treatment medication details were reported. Vaccines placed in refrigerator 13 Jan 2022 Expiration date placed on vials 12 feb 2022 Doses administered to patient 17 feb 2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137356

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 59,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Dose administered after 30-day Use By Date; Dose administered after 30-day Use By Date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after 30-day Use By Date) and PRODUCT STORAGE ERROR (Dose administered after 30-day Use By Date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant and treatment medication details were reported. Vaccines placed in refrigerator 13 Jan 2022 Expiration date placed on vials 12 feb 2022 Doses administered to patient 17 feb 2022

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137353

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 59,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Received expired doses of the Moderna COVID vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired doses of the Moderna COVID vaccine) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired doses of the Moderna COVID vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received expired doses of the Moderna COVID vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication information was not provided by the reporter. Treatment information was not provided by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137353

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 59,0
Geschlecht: M
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Received expired doses of the Moderna COVID vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired doses of the Moderna COVID vaccine) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired doses of the Moderna COVID vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received expired doses of the Moderna COVID vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication information was not provided by the reporter. Treatment information was not provided by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137342

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Patients received expired doses of the Moderna COVID vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients received expired doses of the Moderna COVID vaccine) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients received expired doses of the Moderna COVID vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients received expired doses of the Moderna COVID vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vial was placed in refrigerator on 13-Jan-2022 vaccines. No treatment medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137342

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered

Symptomtext

Patients received expired doses of the Moderna COVID vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patients received expired doses of the Moderna COVID vaccine) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patients received expired doses of the Moderna COVID vaccine). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patients received expired doses of the Moderna COVID vaccine) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vial was placed in refrigerator on 13-Jan-2022 vaccines. No treatment medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137333

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 068H21A

gering

Staat: MI
Alter: 21,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 17.02.2022
Beginn: 17.02.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

Tod: unbekannt Lebensbedrohlich: unbekannt Hospital: unbekannt Disable: unbekannt ER: unbekannt Erholt: nein

Expired product administered Product storage error

Symptomtext

Product storage error; patients who received expired doses of the Moderna COVID vaccine; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Product storage error) in a 21-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 068H21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Product storage error). At the time of the report, EXPIRED PRODUCT ADMINISTERED (patients who received expired doses of the Moderna COVID vaccine) and PRODUCT STORAGE ERROR (Product storage error) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not provided. On 13-Jan-2022 vial was initially stored in the refrigerator. Vial expired on 12-Feb-2022 and administered to patients on 17-Feb-2022. Treatment information was not provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -