VAERS Reports #033F21A

VAERS 2631015

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

kritisch

Staat: -
Alter: 43,0
Geschlecht: M
Eingang: 12.05.2023
Impfdatum: 08.12.2021
Beginn: 06.03.2022
Tage bis Beginn: 88,0
Dosis: 3
Route/Site: IM / LA

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

Acute respiratory failure Myocardial ischaemia Symptom recurrence

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE DEMAND ISCHEMIA ACUTE HYPOXEMIC RESPIRATORY FAILURE 3/29/2022 & 7/13/2022 -- RECURRENCE OF SAME SYMPTOMS

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

VAERS 2602447

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

kritisch

Staat: MN
Alter: 75,0
Geschlecht: M
Eingang: 23.03.2023
Impfdatum: 08.06.2022
Beginn: 22.03.2023
Tage bis Beginn: 287,0
Dosis: 3
Route/Site: IM / LA

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

Death

Symptomtext

Patient expired on 3/22/2023.

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Unknown
Vorgeschichte: COPD, CKD3, HTN, BPH, neurogenic bladder, GERD, osteoarthritis
Andere Medikamente: Unknown
Allergien: NKA
Vorherige Impfungen: -

VAERS 2586373

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

kritisch

Staat: KY
Alter: 73,0
Geschlecht: M
Eingang: 23.02.2023
Impfdatum: 10.11.2021
Beginn: 03.01.2023
Tage bis Beginn: 419,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

PT EXPIRED ON 01/03/2023

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Praegender Schweregrund: Death
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UNKNOWN
Vorgeschichte: HX OF COLON CANCER COPD DM DVT GERD HX OF GI BLEEN HTN L4 VERTABRAL FX
Andere Medikamente: UNKNOWN
Allergien: UNKNOWN
Vorherige Impfungen: -

VAERS 2515298

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

kritisch

Staat: MI
Alter: 56,0
Geschlecht: M
Eingang: 23.11.2022
Impfdatum: 19.11.2021
Beginn: 15.11.2022
Tage bis Beginn: 361,0
Dosis: 3
Route/Site: - / -

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

COVID-19 COVID-19 pneumonia Chest X-ray abnormal Condition aggravated Dysphagia Enteral nutrition Gastrostomy Hypertension Hypotension Hypoxia Intensive care Lung infiltration Pneumonia Pyrexia Respiratory disorder SARS-CoV-2 test positive Septic shock Shock

Symptomtext

Discharge Provider: MD Primary Care Provider: DO Admission Date: 11/15/2022 Discharge Date: Nov 18, 2022 COVID Date: 11/15/2022 PRESENTING PROBLEM: Shock [R57.9] Acute respiratory disease due to COVID-19 virus [U07.1, J06.9] resolved Septic shock COVID Pneumonia History of pseudomonas colonization COPD Prior stroke with resultant apraxia Chronic dysphagia on tube feed HOSPITAL COURSE: The patient is a 57 year old with history of multiple CVA's 10 years ago, COPD, dysphagia, esophageal strictures with chronic feeding tube who presented to ED 11/15 with fever. He had been seen by his PCP 11/14 and prescribed doxycycline for a presumed CAP but his fever persisted so his wife brought him to ED. In ED, he was febrile to 38.9, hypoxic requiring 2 L NC and hypotensive with SBP's in the 80's(baseline 90). He was given 2.5 L IVF, zosyn and started on norepi. He had a CXR with bilateral infiltrates and tested positive for COVID so he was given decadron. He was transferred to ICU for further management of his shock. He was given additional IVF, remdesivir and vanc/zosyn/azithro. His O2 was weaned off so remdesivir and decadron were discontinued. His cortisol was 5, stress dose steroids discontinued 11/17 given resolution of hypotension. Septic shock was attributed to COVID-19 pneumonia with possible secondary bacterial infection. He has known history of pseudomonas colonization Prior sputum culture in 2021 grew Pseudomonas intermediate to Cipro and Zosyn. It was felt that pseudomonas infection is less likely and was transitioned to Augmentin to complete 3 more days course. For COVID-19 pneumonia, he was initially placed on remdesivir and Decadron. These medications were stopped after resolution of hypoxemia and hypertension. After further goal of care discussion, patient wishes to continue aggressive therapy but do not wish to be resuscitated nor does he want to be intubated. He was made do not resuscitate. For dysphagia, he was status post PEG placement and will continue enteral feeding. Patient was evaluated by PT/OT who recommended home with assistance. Patient was discharge in stable condition.

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Praegender Schweregrund: Septic shock
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Acute exacerbation of chronic obstructive pulmonary disease (COPD) COPD (chronic obstructive pulmonary disease) Esophageal stricture Trismus Primary cough headache Chronic pain syndrome Dysphasia Apraxia as late effect of cerebrovascular accident (CVA) Pseudomonas aeruginosa colonization History of CVA with residual deficit Goals of care, counseling/discussion
Andere Medikamente: acetaminophen (TYLENOL) 650 MG extended release tablet ASPIR-LOW 81 MG EC tablet benztropine (COGENTIN) 1 MG tablet budesonide (PULMICORT) 0.5 MG/2ML nebulizer solution Dextromethorphan-guaiFENesin (MUCINEX DM) 30-600 MG TB12 diazePAM (VALI
Allergien: Effexor [Venlafaxine] Norco [Hydrocodone-acetaminophen] Wellbutrin [Bupropion] Aricept [Donepezil] Azactam [Aztreonam In Dextrose Ceftazidime [Cephalosporins] Keflex [Cephalexin] Klonopin [Clonazepam] Morphine Bee Venom Cefepime Statins Topamax [Topiramate]
Vorherige Impfungen: -

VAERS 2431174

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21A

kritisch

Staat: KY
Alter: 64,0
Geschlecht: F
Eingang: 07.09.2022
Impfdatum: 03.11.2021
Beginn: 07.08.2022
Tage bis Beginn: 277,0
Dosis: 3
Route/Site: - / -

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

Acute kidney injury Angiogram cerebral abnormal Arteriogram carotid abnormal Blood creatinine increased Blood magnesium Cerebrovascular accident Chest pain Computerised tomogram abdomen normal Computerised tomogram neck Confusional state Cystitis Cystitis noninfective Depression Encephalopathy Essential hypertension Full blood count Hyperkalaemia Hypokalaemia

Symptomtext

65 y.o. 2/28/1957 Admit Date: 8/7/2022 Discharge Date: 8/16/2022 Principal Diagnoses: Active Problems: Encephalopathy Discharge Diagnosis: Acute metabolic encephalopathy ESBL Proteus UTI Hypotension Hyperkalemia hypokalemia Hypomagnesemia Acute renal failure, prerenal, ACE Left parotitis Possible posterior cerebral CVA Hospital Course: admitted from facility with confusion. Appeared to have UTI, started on antibx, turned to be ESBL as above and changed to meropenem. Creatinine 1.2, above normal baseline. ACE/diuretic held. Betablocker held due to low BP. CTA head and neck done on admit to evaluate her encephalopathy, no occlusion but showed mass left parotid. ? Of posterior cerebral artery CVA. On antibx for this and seen by ENT. CT abdomen benign. She improved with above. Renal functions normalized, mental status cleared. Sx likely primarily from UTI. At discharge baseline, 3 more days of Invanz. Is on statin and APT. Disposition: Discharge Condition: Discharge Medications: Current Discharge Medication List START taking these medications Details acetaminophen (TYLENOL) 325 mg tablet Take 2 Tabs by mouth Every 6 hours as needed for Fever, temp greater than or equal to 100.5F (for oral temperature (or equivalent) of 100.5 degrees Fahrenheit or greater). Refills: 0 Associated Diagnoses: Acute cystitis without hematuria doxycycline monohydrate (MONODOX) 100 mg capsule Take 1 Capsule by mouth Twice a day for 3 days. Refills: 0 Associated Diagnoses: Acute cystitis without hematuria NS (sodium chloride 0.9%) mini-bag 100 mL with ertapenem (INVanz) 1 g Administer 1 g intravenously Every 24 hours for 3 days. Start on 8/17/2022 Indications: inflammation of the bladder, an infection of the skin and the tissue below the skin Refills: 0 Associated Diagnoses: Acute cystitis without hematuria Lactobacillus rhamnosus GG (CULTURELLE) 15 billion cell sprinkle capsule Take 1 Capsule by mouth Twice a day. Qty: 60 Capsule, Refills: 0 Associated Diagnoses: Acute cystitis without hematuria magnesium oxide (MAG-OX) 400 mg tablet Take 1 Tablet by mouth Twice a day for 10 days. Refills: 0 Associated Diagnoses: Acute cystitis without hematuria menthol-zinc oxide (CALMOSEPTINE) 0.44-20.625 % ointment Use as directed Refills: 0 Associated Diagnoses: Acute cystitis without hematuria nystatin (MYCOSTATIN) 100,000 unit/mL suspension Take 5 mL by mouth Four times a day for 7 days. Refills: 0 Associated Diagnoses: Acute cystitis without hematuria pantoprazole (PROTONIX) 40 mg DR tablet Take 1 Tablet by mouth Once Daily for 30 days. Refills: 0 Associated Diagnoses: Acute cystitis without hematuria QUEtiapine (SEROQUEL) 25 mg Take 1 Tablet by mouth Twice a day. Refills: 0 Associated Diagnoses: Acute cystitis without hematuria CONTINUE these medications which have CHANGED Details atorvastatin (LIPITOR) 40 mg tablet Take 1 Tablet by mouth At bedtime for 90 days. Qty: 90 Tablet, Refills: 0 Associated Diagnoses: Cerebrovascular accident (CVA), unspecified mechanism busPIRone (BUSPAR) 5 mg tablet Take 1 Tablet by mouth Three times a day as needed. Refills: 0 Associated Diagnoses: Acute cystitis without hematuria clonazePAM (KLONOPIN) 0.5 mg tablet Take 1 Tablet by mouth Once daily as needed for Anxiety for up to 3 days. Qty: 9 Tablet, Refills: 0 Associated Diagnoses: Anxiety and depression traMADoL (ULTRAM) 50 mg tablet Take 1 Tablet by mouth Every 6 hours as needed for Pain for up to 3 days. Qty: 12 Tablet, Refills: 0 Associated Diagnoses: Acute cystitis without hematuria CONTINUE these medications which have NOT CHANGED Details senna (SENOKOT) 8.6 mg tablet Take 8.6 mg by mouth At bedtime. nystatin (NYSTOP) powder by Topical route Twice a day. polyethylene glycol 3350 (MIRALAX) 17 gram packet Take 17 g by mouth Once Daily. isosorbide mononitrate (IMDUR) 30 mg CR tablet Take 1 Tablet by mouth Once Daily. Qty: 30 Tablet, Refills: 11 clopidogreL (PLAVIX) 75 mg tablet Take 1 Tablet by mouth Daily. Qty: 90 Tablet, Refills: 3 Associated Diagnoses: History of CVA (cerebrovascular accident) loratadine (CLARITIN) 10 mg tablet Take 10 mg by mouth. oxybutynin (DITROPAN-XL) 5 mg ER tablet Take 5 mg by mouth Daily. aspirin (ASPIRIN) 81 mg DR tablet Take 1 Tab by mouth Daily. Refills: 0 Associated Diagnoses: Essential hypertension; Atypical chest pain dicyclomine (BENTYL) 20 mg tablet Take 20 mg by mouth Twice a day. escitalopram oxalate (LEXAPRO) 20 mg Take 1 Tab by mouth Daily. Qty: 30 Tab, Refills: 2 Associated Diagnoses: Anxiety and depression amitriptyline (ELAVIL) 50 mg tablet Take 1 Tab by mouth At bedtime. Qty: 30 Tab, Refills: 2 Associated Diagnoses: Anxiety and depression levothyroxine (SYNTHROID) 50 mcg tablet Take 1 Tab by mouth Daily. Qty: 30 Tab, Refills: 2 Budesonide-Formoterol (SYMBICORT 160-4.5 MCG) 160-4.5 mcg/Actuation inhaler Take 2 Puffs by inhalation Every 12 hours. clobetasoL (TEMOVATE) 0.05 % cream Apply twice daily after soaks, then immediately apply Cetaphil or CeraVe cream all over. Do not use on face, underarms, breast or groin. Qty: 45 g, Refills: 1 Associated Diagnoses: LSC (lichen simplex chronicus) halobetasol (ULTRAVATE) 0.05 % cream Apply twice daily after soaks, then immediately apply Cetaphil or CeraVe cream all over. Do not use on face, underarms, breast or groin. Qty: 50 g, Refills: 1 Associated Diagnoses: LSC (lichen simplex chronicus) nitroglycerin (NITROSTAT) 0.4 mg SL tablet Take 1 Tab sublingually Every 5 minutes as needed for Chest pain. Qty: 30 Tab, Refills: 0 Associated Diagnoses: Atypical chest pain STOP taking these medications potassium chloride (KLOR-CON) 20 mEq tablet Comments: Reason for Stopping: carvediloL (COREG) 6.25 mg tablet Comments: Reason for Stopping: famotidine (PEPCID) 20 mg tablet Comments: Reason for Stopping: hydrochlorothiazide (HYDRODIURIL) 25 mg tablet Comments: Reason for Stopping: Diabetic diet AAT Mid line out after antibx finished CBC CMP Mg++ within 3-5 days BP meds held due to low BP, resume as indicated CT neck 2 weeks, follow up ENT after Resume PT/OT

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

VAERS 2290018

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

kritisch

Staat: IL
Alter: 85,0
Geschlecht: M
Eingang: 22.05.2022
Impfdatum: 15.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 6,0
Dosis: 1
Route/Site: IM / -

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

Acute respiratory failure Angiogram pulmonary abnormal Blood lactic acid increased C-reactive protein increased COVID-19 Complication associated with device Computerised tomogram thorax abnormal Death Dysphagia Dyspnoea Fibrin D dimer increased Hypoxia Pneumonia Productive cough Pulmonary embolism SARS-CoV-2 test positive Sputum discoloured Superficial vein thrombosis

Symptomtext

COVID Vaccine Breakthrough CAse Moderna Dose 1 11/15/21 (033F21A) COVID Positive 11/30/21 12/1/21: Patient has dementia. He also has myasthenia gravis and hypothyroidism.Not a very reliable historian. He reportedly tested positive for SARS-CoV-2 10 days ago. Having cough with yellowish expectoration. Family think that he may have aspirated in a.m. Family noticed increased work of breathing in last 1 day. He had temperature of 100.3? F in emergency department. Was hypoxic and was requiring up to 5 L of oxygen in emergency department. Had elevated lactic acid level. CRP was 16.25. His D-dimer was very very high at 35.2. CT pulmonary angiogram showed bilateral pulmonary emboli. 12/10/21: 85-year-old male patient with a history of severe dementia, myasthenia gravis and hypothyroidism was admitted the hospital with complaints of cough. The patient was diagnosed with COVID-19 infection obtained side to admission to the hospital on 12/2/2021. Patient was noted to have some shortness of breath and elevated body temperature is 100.3? F. He was also hypoxic requiring 5 L of oxygen in the emergency room on admission. CT of the chest showed evidence of bilateral PE E the patient was admitted for further care. Acute hypoxic respiratory failure the the -secondary due to COVID-19 and pneumonia -patient maintained on oxygen -patient completed treatment with steroids, remdesivir and antibiotics treating COVID-19 infection Bilateral PE with right lower extremity superficial thrombus -patient nt on ay medications as he is discharged home on no medication -Pt under palliative care at home now and then hospice care eventually after d/c to home per the son Dysphagia -patient followed by dietitian, recommend puree diet with honey thickened fluids, continue Severe dementia -patient son is the power of attorney Catheter associated trauma, off antibiotics at the time of discharge. Discussed the patient's case with care coordination again this morning. The son, power of attorney wishes for the patient to be transferred home. Patient will have a 24 hour attendant/nurse at home. Outpatient palliative care to follow the patient at home. The son will consider hospice at a later point after the patient is discharged home. All questions answered. 12/13/21: Patient deceased

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 10,0
Labordaten: -
Aktuelle Erkrankungen: dementa myasthenia gravis hypothyroidism
Vorgeschichte: dementa myasthenia gravis hypothyroidism
Andere Medikamente: erythromycin eye ointment QID pyridostigmine 60 mg PO TID
Allergien: NKA
Vorherige Impfungen: -

VAERS 2254701

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

kritisch

Staat: MI
Alter: 48,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 26.01.2022
Beginn: 17.04.2022
Tage bis Beginn: 81,0
Dosis: 3
Route/Site: IM / -

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

Acute kidney injury Acute respiratory failure Alanine aminotransferase increased Aortic valve incompetence Aspartate aminotransferase increased Blood alkaline phosphatase increased Blood bilirubin decreased Brain natriuretic peptide increased COVID-19 COVID-19 pneumonia Cardiac failure congestive Cardiorenal syndrome Chest X-ray abnormal Chronic obstructive pulmonary disease Condition aggravated Congestive hepatopathy Cough Echocardiogram abnormal

Symptomtext

"Hospitalized (4.17.22 -4.19.22); COVID-19 positive (4.17.22); fully vaccinated PLUS Booster - moderna x3 d/c summary: BRIEF OVERVIEW: Discharge Provider: MD Primary Care Provider: PA-C Admission Date: 4/17/2022 Discharge Date: Apr 19, 2022 Active Hospital Problems Diagnosis Date Noted POA ? Acute on chronic respiratory failure with hypoxia and hypercapnia Discharge Disposition: home or self care Active Issues Requiring Follow-up: - follow up with PCP: CHF exacerbation, re-evaluate lasix regimen following continued diuresis, COPD, and COVID follow up DETAILS OF HOSPITAL STAY: PRESENTING PROBLEM: Acute on chronic respiratory failure with hypoxia and hypercapnia [J96.21, J96.22] HOSPITAL COURSE: Patient is a 49 y.o. female with a PMH of T2DM, COPD on 4L Baseline, OSA who presented to the ED due to worsening generalized fatigue, cough over the past week found to be requiring 6L of O2 and fluid overloaded on exam., found to be Covid positive, with CXR revealing GGO transferred to Hospital for further mangement. Patient was treated with diuresis for heart failure exacerbation, duonebs and azithromycin for coverage for COPD exacerbation and decadron for COVID 19 pneumonia diagnosis. Patient was evaluated with updated echo inpatient, showing stable findings with updated EF of 65% with mild valvular stenosis and mild aortic regurgitation compared to Oct 2021. Following IV diuresis, patient's clinical status improved and her oxygen requirements improved back to baseline 4L both at rest and with ambulation. During presentation, patient had an AKI that improved with diuresis supporting cardiorenal etiology. Patient was discharged with an increased diuresis regimen from her previously daily home dosing. Prior to discharge on 4/19, patient was counseled on resources with COVID-at-home program for follow-up. However, she declined service and expressed preference to quarantine at home and call her PCP for close outpatient follow up. Consult Orders (From admission, onward) IP CONSULT TO DIABETES & ENDOCRINOLOGY Provider: Diabetes And Endocrinology INPATIENT PROCEDURES: none BP 178/82 | Pulse 52 | Temp 36.9 ?C (Oral) | Resp 16 | Ht 1.626 m | Wt 105 kg | SpO2 98% | BMI 39.73 kg/m? FIO2 (%): 35 % Physical Exam Constitutional: Appearance: She is obese. HENT: Head: Normocephalic and atraumatic. Right Ear: External ear normal. Left Ear: External ear normal. Nose: Nose normal. No congestion or rhinorrhea. Mouth/Throat: Mouth: Mucous membranes are moist. Pharynx: Oropharynx is clear. Eyes: Conjunctiva/sclera: Conjunctivae normal. Cardiovascular: Rate and Rhythm: Normal rate and regular rhythm. Pulses: Normal pulses. Heart sounds: Normal heart sounds. Pulmonary: Effort: Pulmonary effort is normal. No respiratory distress. Breath sounds: Normal breath sounds. No wheezing. Abdominal: General: Abdomen is flat. Bowel sounds are normal. There is no distension. Palpations: Abdomen is soft. Tenderness: There is no abdominal tenderness. Musculoskeletal: Right lower leg: Edema present. Left lower leg: Edema (mild B/l LE Edema 1-2+, improving on discharge) present. Skin: General: Skin is warm. Capillary Refill: Capillary refill takes less than 2 seconds. Findings: No erythema, lesion or rash. Neurological: Mental Status: She is alert and oriented to person, place, and time. Mental status is at baseline. Psychiatric: Mood and Affect: Mood normal. Behavior: Behavior normal. 4/17/22 H&P: CHIEF COMPLAINT: Acute on chronic respiratory failure with hypoxia and hypercapnia ASSESSMENT / PLAN: Patient is a 49 y.o. female with a PMH of T2DM, COPD on 4L Baseline, OSA who presented to the ED due to worsening generalized fatigue, cough over the past week found to be requiring 6L of O2 and fluid overloaded on exam, found to be Covid positive, with CXR revealing GGO transferred to Hospital for further mangement. #Acute on Chronic Hypoxic Hypercapnic Respiratory Failure-Multifactorial Pt with increasing O2 requirements from baseline 4L, currently on 7L NC. Etiology of patients respiratory failure likely multifactorial in the setting of CHF exacerbation, COPD exacerbation, and Covid Pneumonia with GGO notable on CXR with b/l infiltrates noted. Will plan on managing each condition as written below. Plan: -on 7L NC, wean as able -other management as noted below #Acute on Chronic Diastolic Heart Failure Exacerbation BNP elevated at 7,012 on arrival. CXR with b/l GGO notable, with physical exam consistent with fluid overload. Now s/p 40 IV lasix at hospital with significant response and good UOP. Bedside ultrasound revealed a IVC 2-2.5cm with minimal respiratory variation consistent with fluid overload. On home lasix 20 daily, will plan on initiating 40 IV Lasix BID. Plan: -Echo ordered -DSW, strict IO/s -Lasix 40 IV BID #COPD Exacerbation- On 4L at baseline Notable wheezing on exam, in the setting of covid 19 pneumonia and fluid overload may have triggered pt into exacerbation. Plan: -Decadron 6mg daily -Azithromycin -Scheduled duonebs -Singulair, Spiriva, Flovent #Covid-19 Pneumonia Patient Vaccinatedx3. With increased O2 requirements currently on HFNC , will plan on treating at this time with decadron 10d course. Will hold off on Remdesivir in the setting of AKI and elevated LFT's. Cannot rule out superimposed bacterial infection with increased sputum production and change in color. Will order nfectious workup with sputum cx, legionella and strep pneumo, await findings prior to broadening abx. Plan: -Wean O2 as able, goal O2 88-92 -Decadron 6mg daily for 10d course -Legionella step urine ag -Sputum cx ordered #AKI Baseline Creatinine near 0.95. Cr on presentation 2.08. Significant response to 40 IV lasix, with improvement in kidney function signals likely cardiorenal syndrome in the setting of fluid overload. Will plan on Continuing to monitor response to diuresis at this time. Plan: -BMP Q8 -Continue diuresis #Hyponetremia Likely Hypervolemic Hyponatremia. Will plan on diuresis at this time, fluid restriction. Plan: -Diuresis, fluid restriction -BMP q8 #T2DM On Lantus 25 units and Metformin 1G BID daily and novolog 10 w/ meals. Will polan on initiating home dose Lantus, with MDC, close monitoring of Blood sugars. Plan: -Lantus 25, Moderate dose corrective #Elevated Liver Enzymes AST 261, ALT 107, T bili 0.2, ALK Phos 359 on arrival. Known hx of hepatic steatosis seen on imaging. Elevated enzymes from baseline currently, likely in the setting of hepatic congestion w/ fluid overload, and covid infection. Plan: -Daily CMP -IF worsening can consider RUQ u/s #Microcytic Anemia Baseline Hgb near 13. Currently 11.5. Will plan on evaluating with iron studies Plan: -Ferritin, Iron studies pending #Fibromyaligia -home lyrica #Bipolar Disorder -Lamictal, Lexapro #Insomnia -Home remeron #HTN On home norvasc Plan: -Will hold off initiating home med now in he setting of diuresis, BP remains stable

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Praegender Schweregrund: Acute respiratory failure
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Past Medical History: Diagnosis Date ? Anxiety ? Asthma ? Bipolar 1 disorder ? Bipolar disorder, unspecified ? COPD (chronic obstructive pulmonary disease) ? CPAP (continuous positive airway pressure) dependence ? Depression ? Diabetes mellitus ? Headache(784.0) ? Hypertension ? Kidney disease ? Obesity ? OSA (obstructive sleep apnea) ? Oxygen dependent 4L per NC ? Posttraumatic stress disorder ? Undiagnosed cardiac murmurs
Andere Medikamente: Albuterol Sulfate 108 (90 Base) MCG/ACT 2 puffs Inhalation Every 4 hours PRN amLODIPine Besylate 5 mg Oral Daily Ergocalciferol 50,000 Units Oral Weekly, friday Escitalopram Oxalate 10 mg Oral Daily Fluticasone Propionate 50 MCG/ACT 2 spray
Allergien: coritzone - swelling lidocaine - swelling
Vorherige Impfungen: -

VAERS 2072200

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

kritisch

Staat: MD
Alter: 88,0
Geschlecht: M
Eingang: 28.01.2022
Impfdatum: 07.01.2022
Beginn: 15.01.2022
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: IM / RA

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

Death

Symptomtext

Resident expired on 1/15/2022, 5:42 AM

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

VAERS 2037841

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

kritisch

Staat: PA
Alter: 66,0
Geschlecht: M
Eingang: 15.01.2022
Impfdatum: 15.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / AR

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

Anticoagulant therapy Chest pain Computerised tomogram thorax abnormal Dyspnoea Pulmonary embolism

Symptomtext

Pulmonary Embolus, Hospitalized, treated with heparin, then rivaroxaban. Initially short of breath and chest pain, now asymptomatic.

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Praegender Schweregrund: Pulmonary embolism
Hospital-Tage: 2,0
Labordaten: CT chest on 11-29-2021
Aktuelle Erkrankungen: celiac disease
Vorgeschichte: hyperlipidemia, sleep apnea
Andere Medikamente: atorvastain
Allergien: NKA
Vorherige Impfungen: -

VAERS 1909820

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

kritisch

Staat: MD
Alter: 50,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 30.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Atrial fibrillation Electrocardiogram abnormal Myocardial infarction

Symptomtext

Report of AFIB on 11/22/2021, went to the Dr and had EKG said shows signs of past Heart Attack

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Praegender Schweregrund: Myocardial infarction
Hospital-Tage: -
Labordaten: EKG 11/23/2021
Aktuelle Erkrankungen: Fibromyalgia/Rheumatoid Arthritis
Vorgeschichte: Allergies, Arthritis
Andere Medikamente: Vitamin C 500 mg, Vitamin D 25 mcg, Voltaren 1% gel, modafinil 200 mg, multivitamin, durolane 60 mg as needed, singulair 10 mg, Omeprazole 40 mg, Clindamycin 1% external swab, Dapsone 7.5 %, Duloxetine 30 mg, Famotidine 40 mg, Frova 2.5 m
Allergien: Gold, Nickel, Silver, IVP, Latex, Sulfa drugs, Prednisone mood problems.
Vorherige Impfungen: -

VAERS 2594720

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: VA
Alter: 70,0
Geschlecht: M
Eingang: 10.03.2023
Impfdatum: 19.11.2021
Beginn: 26.07.2022
Tage bis Beginn: 249,0
Dosis: 3
Route/Site: IM / LA

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

Echocardiogram normal Ischaemic cerebral infarction Ischaemic stroke Laboratory test normal Magnetic resonance imaging head abnormal Paraesthesia

Symptomtext

Patient suffered acute ischemic stroke on 7/26/22. The symptoms were mild at onset and involved intermittent paresthesias in R face. Went to ED and was admitted overnight. Brain MRI showed ischemic infarcts in the deep white matter. Embolic workup with echo and carotids clear. Symptoms resolved quickly. He is absolutely convinced the Moderna vaccine given in Nov 2021 caused this and demanded that an event report be filed with VAERS.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Ischaemic stroke
Hospital-Tage: 1,0
Labordaten: Brain MRI 7/26/22 at hospital.
Aktuelle Erkrankungen: hypertension, rosacea, gerd, barrett's esophagus
Vorgeschichte: same as above
Andere Medikamente: losartan-hctz, indomethacin, aspirin EC, metoprolol succinate, doxycycline, pantoprazole, topical oxymetazoline
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2546975

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: TX
Alter: 37,0
Geschlecht: F
Eingang: 30.12.2022
Impfdatum: 29.12.2021
Beginn: 05.02.2022
Tage bis Beginn: 38,0
Dosis: 3
Route/Site: SYR / LA

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

Computerised tomogram head abnormal Electric shock sensation Laboratory test Magnetic resonance imaging head abnormal Pain Trigeminal neuralgia

Symptomtext

My symptoms started on February 05, 2022 I woke up & I had an electric shock feeling through my arm it also went through the 3rd branch of my face (right side) the pain traveled from the right to the left pain level would be on a scale of 20. I was hospitalized on February 15, 2022 I was released on February 16, 2022 and was diagnosed with Trigeminal Neuralgia. I was prescribed carbamazepine for my symptoms and I also take LYRICA as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Electric shock sensation
Hospital-Tage: 1,0
Labordaten: Lab work 02/15/2022, MRI 02/15/2022, Cat scan 02/15/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2504580

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: OH
Alter: 41,0
Geschlecht: M
Eingang: 10.11.2022
Impfdatum: 19.01.2022
Beginn: 06.11.2022
Tage bis Beginn: 291,0
Dosis: 3
Route/Site: - / -

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

Acute respiratory distress syndrome COVID-19 Chills Cough Dyspnoea Intensive care Pneumonia Pyrexia SARS-CoV-2 test positive

Symptomtext

Tested positive for COVID-19, resulted in hospital admission. Symptoms include fever, subjective fever, chills, cough, and shortness of breath. The patient developed pneumonia, acute respiratory syndrome, and admission into ICU.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute respiratory distress syndrome
Hospital-Tage: -
Labordaten: Nasopharyngeal swab collected 11/06/2022 detected 2019 Novel Coronavirus RNA on 11/7/2022.
Aktuelle Erkrankungen: -
Vorgeschichte: Chronic lung disease, immunocompromised, former smoker, and autoimmune condition.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2440078

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: SC
Alter: 56,0
Geschlecht: F
Eingang: 11.09.2022
Impfdatum: 05.11.2021
Beginn: 26.12.2021
Tage bis Beginn: 51,0
Dosis: UNK
Route/Site: - / AR

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

Blood test Computerised tomogram normal Gait inability Guillain-Barre syndrome Lumbar puncture Magnetic resonance imaging normal Mechanical ventilation Paralysis

Symptomtext

Contracted Guilliane Barre Went into the hospital on January 7, 2022; after becoming paralyzed from the chest down; put on ventilator to breathe for 6 days; had to learn to walk again; left hospital on February 22, 2022. Still suffering from some residual effects.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 46,0
Labordaten: Lumbar puncture January 8 or 9 CT scan January 7 Negative MRI January 8 Negative Bloodwork everyday
Aktuelle Erkrankungen: -
Vorgeschichte: Diabetes High blood pressure High cholesterol
Andere Medikamente: Welchol Hydrochlorothiazide Pantoprazole Metformin Januvia Prevastatin Lisinopril Bupropion Amlodipine Aripiprazole
Allergien: None
Vorherige Impfungen: -

VAERS 2278270

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: NJ
Alter: 42,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 02.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Full blood count normal Injection site erythema Loss of consciousness Pregnancy test negative Pruritus Toxicologic test normal Urticaria

Symptomtext

Almost immediately after receiving the vaccine I got injection site redness which is pretty normal for me so I wasn't concerned. But within 48 hours I began to get itchy hives on my neck, chest, and face which began to spread to full body. Antihistamines were helping sometimes, but not every time. Since then, I have been experiencing daily bouts of hives and strange dermatological issues like redness appearing in the shape of scratches on my stomach and other parts of my body or random spots of itchiness in my face and hair line. It seems to be unpredictable on when it will flare up. It seems to be primarily on my face and chest but also on the bottom of my feet on and on my hands. I have tried antihistamine creams as well that haven't really worked either. It has been going on long enough at this point that I have set up an appointment to have full blood panels done to try to determine a cause. Also, around a month ago, I passed out and my daughter called EMS and I was transported my ambulance to the local hospital where I was evaluated and they advised that you hydrate and monitor for any future issues.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: Full blood panel, tox screen, pregnancy test, all tests came back normal 03/28/2022.
Aktuelle Erkrankungen: None.
Vorgeschichte: Hypothyroidism
Andere Medikamente: Synthroid; multivitamin; vitamin D
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2275864

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: KY
Alter: 53,0
Geschlecht: F
Eingang: 13.05.2022
Impfdatum: 11.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: SYR / RA

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

Adverse event Arthritis Cyanosis Haemorrhage Limb mass Loss of personal independence in daily activities Pain in extremity Pain of skin Skin discolouration Skin exfoliation Swelling Thrombosis Vascular test normal X-ray limb abnormal

Symptomtext

I received my booster shot on 11/11/2021 and adverse event on 11/28/2021 2-3 weeks after. I noticed in the morning while I was taking shower I felt that something wrong with my toe. I felt some kind of lump on my toes. I felt like it was coming out of my toes. The toe became swollen, very painful, the lumps of my toe would move and change and then my toe became blue. Then I noticed a large lumps on my toe. It was blood in the lump. The doctors told me that a blood clot got into my toe. My cap or capillary vain that flow blood to my lungs could have caused it but he wasn't sure. He send me to a podiatrist and send me to get x-ray. My doc had no idea how to treat it. The x-ray came back and there is nothing was there. Except for arthritis was in my joint. The podiatrist had no idea what to do. He gave me some pain medication for my toe. He send me to the hospital for vascular test for my extremities ( chest). No negative results were shown. There is no reason found behind it. I went back to my PCP, I showed him my test result I told him about the podiatrist. My PCP gave me different pain medication. ( hydrocodone pain killers which didn't work. Then he referred me to a cardio vascular specialist. I told him that the medication my PCP gave me wasn't working. I have difficult with everything I do. My toe hurt when I walk, my toe hurt when I sit. My toe change colors and move. Swollen eventually went away, the lump became a dot. I had sore on my right side of the toe then I went to my PCP. He gave me more medication it went away. Then another one came after about 4 months, my toe shattered to change again it looked like diabetic toe. My toe was healing. I woke up one morning the dot bottom of my foot went way it healed. The skin top of my toe came off. The new skin was tender. My toe is almost normal. This entire process took 4 and half month to 5 months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: x-ray, chest test
Aktuelle Erkrankungen: none
Vorgeschichte: rhinos disease
Andere Medikamente: metoprolol, corapine, Synthroid 112micrograms, vimrine 21mg, abcrm 12 milligrams, copalaoe, multivitamin, biotin, vitamin d3 supplements, melatonin.
Allergien: allergic to gold, some adhesive
Vorherige Impfungen: -

VAERS 2264750

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 08.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: SYR / LA

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

Chronic spontaneous urticaria Syncope

Symptomtext

Approximately 2 weeks after my booster shot I developed chronic spontaneous urticaria and am still experiencing it 5 months later. I also had a fainting incident the day my symptoms started and had to go to the ER.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lexapro 10 mg
Allergien: None
Vorherige Impfungen: -

VAERS 2255205

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: IN
Alter: 39,0
Geschlecht: F
Eingang: 27.04.2022
Impfdatum: 12.11.2021
Beginn: 10.01.2022
Tage bis Beginn: 59,0
Dosis: 3
Route/Site: SYR / RA

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

Arterial injury Blood test abnormal COVID-19 Cardiac dysfunction Cardiac imaging procedure normal Catheter placement Cough Electrocardiogram Exposure to SARS-CoV-2 Fatigue Gait inability General physical health deterioration Intensive care Malaise Movement disorder Myocarditis Poor peripheral circulation Pyrexia

Symptomtext

Around January 10, 2022 I had very mild symptoms of COVID-19, but I tested negative for it. I felt tired and I had a little bit of a cough. My husband had some mild symptoms as well, and he tested positive for COVID-19. I believe I went to a local place in town where I got a false negative COVID-19 test. I just assumed that I had COVID-19 at that point. I felt better for about a week and then I felt tired. I had developed a fever. I decided to go to the walk-in clinic. They listened to my heart and ran an electrocardiogram. Then they sent me to the ER immediately. The doctors said I have myocarditis and then they hospitalized me. Then it gets blurry because I started to decline quickly. I ended up in the intensive care unit. They did a catheterization. My blood test kept showing very, very high levels of troponin. My heart went to 10% capacity. The doctors put an Impella heart device in me. They thought they would have to do a transplant or biopsy on me, but they wouldn't of have been able to do it there, so I was airlifted to another facility to get the transplant or biopsy if needed. I got to the second facility 6 days later. They didn't have to do a transplant or a heart biopsy. They said that it looked like my heart was fighting to keep beating. Then I kind of bounced back. Nobody knows why I bounced back so quickly. By January 2, 2022 I was released from the hospital. I wasn't able to move at all at first. I had to learn how to walk again. I went from a walker to a cane in the hospital. I am no longer using those anymore. I have a team of cardiologist that are walking with me. I go to cardio rehab 3x day. I was told that my femoral artery was damaged by the heart pump because it was not allowing blood and oxygen to flow to my leg properly. The last MRI shows no structural damage done to my heart. The doctors are wondering if the small blood vessels around the heart were damaged. Treating facility said that the heart device saved my life. They also said they know I had COVID-19 because it kept coming negative at first but then the test finally started showing up as positive. I was prescribed Lisinopril 2.5mg 1x day, Klor-Con M20 1x day, Metoprolol Succinate 12.5mg 1x day, Furosemide 20mg as needed, and Buspirone 5mg 3x day. The doctors told me to stop taking the birth control so I am no longer on it. I was hospitalized from January 20, 2022 to February 2, 2022 at both the first hospital and the second.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Intensive care
Hospital-Tage: 14,0
Labordaten: COVID-19 Tests ? Negative; COVID-19 Tests ? Positive; Catheterization; Electrocardiogram; MRI ? shows no structural damage done to my heart.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: Generic of Seasonique birth control.
Allergien: None.
Vorherige Impfungen: -

VAERS 2180105

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: IL
Alter: 72,0
Geschlecht: M
Eingang: 15.03.2022
Impfdatum: 12.11.2021
Beginn: 20.01.2022
Tage bis Beginn: 69,0
Dosis: 3
Route/Site: IM / LA

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

Acute kidney injury Anaemia Anticoagulant therapy Blood loss anaemia COVID-19 COVID-19 pneumonia Chest X-ray abnormal Chronic kidney disease Condition aggravated Culture positive Deep vein thrombosis Endotracheal intubation Gastrostomy Haemoglobin normal Haemorrhage Hypotension Laboratory test Lung consolidation

Symptomtext

Patient received moderna vaccine on 3/10/21, 4/9/21, and 11/12/21. Found to be COVID19 positive on 1/20/22. transferred for worsening respiratory failure secondary to COVID-19 pneumonia. Patient is vaccinated, he did test positive on 01/20/2022, symptom onset was 01/17/2022 and was hospitalized on once 01/26/2022. He also did develop Aki on CKD stage IIIA. Was being treated with remdesivir baricitinib, Decadron. He did have a V/Q scan which did reveal low probability of PE. After transfer patient was placed on BiPAP, continued to have worsening respiratory failure and eventually required intubation on 02/02/2022. Eventually was pegged and trached on 2 15 2022. Ultrasound of lower extremities did reveal a right lower extremity DVT therefore was started on therapeutic anticoagulation after which she did develop bleeding with acute blood loss anemia likely secondary to retroperitoneal hemorrhage. Anticoagulation was withheld the resumed after which he did develop anemia again. He required multiple PRBC transfusions. He eventually had IVC filter placed on 02/14/2022. Patient did have superimposed bacterial pneumonia and was treated with broad-spectrum antibiotic therapy, restarted having fevers on 02/10/2022. Repeat cultures did reveal growth of yeast in sputum. He did develop she shock likely a combination secondary to sepsis as well as hemorrhage from the retroperitoneal bleed and required pressors transiently. Did complete course of vancomycin, Zosyn and micafungin. Nephrology was consulted for the Aki on CKD stage IIIA which improved and was likely secondary to medications, shock. Hemoglobins have remained stable, blood pressure is low normal and has required intermittent boluses of normal saline. He was weaned of sedation and is able to follow commands and does not have any focal neurological deficits. Will be transferred in stable condition to LTAC in hopes of weaning off ventilator. At time of discharge patient's ventilator requirements were FiO2 of 35% and PEEP of 8. His anti-platelet therapy was discontinued which include aspirin and Plavix, patient may be resumed on prophylactic Lovenox for DVT while monitoring hemoglobins. His antihypertensives were also discontinued due to borderline low blood pressures. Discharged on 2/25/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Deep vein thrombosis
Hospital-Tage: 26,0
Labordaten: 1/20/22 COVID19: positive 1/30/22 chest xray: Extensive in diffuse consolidative changes right worse than left lungs described above without pleural effusions. Findings may reflect pulmonary edema with atypical infectious process not excluded. Clinical correlation and follow-up necessary.
Aktuelle Erkrankungen: -
Vorgeschichte: Acute kidney injury, Congestive heart failure, History of hip replacement, Skin cancer, and Throat cancer. coronary disease status post CABG, COPD non oxygen dependent, CKD stage 3 a, CHF-uncertain type, hypertension, hyperlipidemia, hypothyroidism , history of carcinoma of the mouth/throat
Andere Medikamente: albuterol 108 (90 Base) MCG/ACT Aers Commonly known as: PROVENTIL HFA, VENTOLIN HFA 4 Puffs, Inhalation, EVERY 2 HOURS PRN allopurinol 300 MG Tabs Commonly known as: ZYLOPRIM 300 mg, Oral, NIGHTLY atorvastatin 20 MG Tabs Commonly known
Allergien: none
Vorherige Impfungen: -

VAERS 2110140

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: MI
Alter: 68,0
Geschlecht: F
Eingang: 14.02.2022
Impfdatum: 19.11.2021
Beginn: 04.01.2022
Tage bis Beginn: 46,0
Dosis: 3
Route/Site: UN / UN

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

Asymptomatic COVID-19 Behaviour disorder Bradycardia Echocardiogram normal Emotional disorder Influenza A virus test negative Influenza B virus test Loss of consciousness Respiratory syncytial virus test negative SARS-CoV-2 test positive

Symptomtext

68y.o. female with a PMH of bipolar affective disorder, HTN, HLD, anxiety, and depression who was transferred to (Privacy) from (Privacy) after concern for an episode of transient loss of consciousness it was felt that her symptoms were likely related to hypotension associated with Seroquel. Medication was adjusted. Symptoms resolved. She did have intermittent bradycardia which was asymptomatic. Echocardiogram did not show any significant findings. She did test positive for COVID-19 virus on 1/4/2022. She was asymptomatic. She was accepted back to the general psychiatric unit for further management of her emotional/behavioral disorder. Time spent in care, counseling and discharge on date of discharge-33 minutes

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: 14,0
Labordaten: Results Covid-19, Flu, RSV by NAA Contains abnormal data Covid-19, Flu, RSV by NAA Order: (Privacy) Status: Final result Visible to patient: Yes (not seen) Next appt: None Specimen Information: Nasopharyngeal; Swab 0 Result Notes Component Ref Range & Units Influenza A Not Detected Not Detected Influenza B Not Detected Not Detected RSV Not Detected Not Detected SARS-CoV-2 (COVID-19) by NAA, Micro Not Detected Detected Abnormal Narrative Methodology: Nucleic Acid Amplification(NAA)/Polymerase Chain Reaction(PCR) The SARS-CoV-2 (COVID-19) test is for in vitro diagnostic use under the Emergency Use Authorization (EUA) for (Privacy) laboratories certified to perform high complexity testing. This test has not been cleared or approved. Specimen Collected: 01/04/22 2:19 PM Last Resulted: 01/04/22 3:57 PM
Aktuelle Erkrankungen: Activity not at all limited SELF ADL , BELONGS TO GYM BUT HAS NOT WORKED OUT LATELY, COOKING , CLEANING ? Anxiety ? Arthritis RIGHT HAND ? Depression ? Gastroesophageal reflux disease ? Hypertension STABLE ? Hypoglycemia ? IBS (irritable bowel syndrome
Vorgeschichte: -
Andere Medikamente: ARIPiprazole (ABILIFY) 5 MG PO Tab take 1 Tablet by mouth once daily. Unknown Unknown time aspirin (ECOTRIN) 81 MG PO Tablet Delayed Response take 1 Tablet by mouth once daily. Unknown Unknown time atorvastatin (LIPITOR) 10 MG PO Tab take 1
Allergien: ? Pcn [Penicillins] Other PASSED OUT FROM IM SHOT ? Perfumes [Aromatic Oils] Other NAUSEA
Vorherige Impfungen: -

VAERS 2105147

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: MA
Alter: 42,0
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: 04.11.2021
Beginn: 24.01.2022
Tage bis Beginn: 81,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal discomfort Annuloplasty Atrial enlargement C-reactive protein increased Cardiac imaging procedure abnormal Cardiac tamponade Echocardiogram Echocardiogram abnormal Ejection fraction decreased Electrocardiogram ST segment abnormal Inferior vena cava dilatation Laboratory test abnormal Left ventricular dysfunction Pericardial effusion Pericardial fibrosis Pericarditis Red blood cell sedimentation rate increased Right ventricular dysfunction

Symptomtext

Patient received Covid-19 Pfizer vaccine on 3/26 and 4/16/21 and the Covid-19 Moderna booster dose on 11/4/21. Patient presented to BWH on 1/24/22 after OP echo revealed interval worsening of pericardial effusion with tamponade physiology on formal TTE. Patient had an episode of positional abdominal discomfort and was diagnosed with pericarditis on 1/20/21 based on EKG and labs. Patient began on colchicine and ibuprofen for medical management with improvement in symptoms. Patient found to have diffuse ST changes consistent with pericarditis. Patient completed a course of ibuprofen with plan for outpatient cardiology re assessment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: 6,0
Labordaten: ESR on 1/26/22: 55 mm/h, CRP on 1/26/22: 59.9 mg/L, Troponin T on 1/24/22: 14ng/L, MRI cardiac on 1/28/22: IMPRESSIONS: 1. There is a concentric thickening of pericardium measuring 7.0 mm. The pericardium is enhancing on T2 weighted images. It is also enhancing post-contrast indicating ongoing inflammation. There are some signs of pericardial constrictive physiology with tubular shaped right ventricle, atrial enlargement and dilated IVC. There is a trivial loculated pericardial effusion. 2. The left ventricular size is normal. The left ventricular ejection fraction is 41 % by Simpson's method. Global left ventricular function is mild-moderately decreased. There is paradoxical septal motion consistent with post-operative state. The left ventricular mass is normal. 3. Pharmacologic stress CMR was performed with the regadenoson vasodilator protocol. Peak HR achieved during stress was 130 bpm and peak blood pressure was 131/85 mm Hg. No chest pain or shortness of breath was reported. There is no regadenoson induced first pass myocardial perfusion defect. 4. There is no resting first pass myocardial perfusion defect. There is no evidence of myocardial edema by T2 weighted imaging. Native T1 values are mildly elevated: 1305 - 1320 MS (Normal range: 1200 +/- 80ms on 3T scanner). Extracellular volumes are normal: 27 - 31% (Normal range: 27 - 32%). 5. The right ventricle is tubular shaped and normal in size. Right ventricular ejection fraction is 43% by Simpson's method. Global right ventricular function is mildly decreased. The right ventricular wall is diffusely hypokinetic. 5. There is no late gadolinium enhancement to suggest prior infarct, inflammation, or infiltration of the LV and RV myocardium. 6. Left atrial size is normal. Right atrial size is mildly enlarged. 7. Mitral annuloplasty ring in situ. No residual mitral regurgitation. There is mild tricuspid regurgitation. CONCLUSIONS: Collectively, these findings are consistent with abnormally thickened pericardium with active pericardial edema and inflammation with some evidence of pericardial constriction. Mild-moderately reduced left ventricular systolic function (LVEF: 41%) without evidence of inducible ischemia, infarction or fibrosis. ECHO on 1/26/22: There is moderate-depressed LV systolic function (LVEF 35-40%) without obvious regionality. The RV is mildly hypokinetic. The appearance of the mitral valve is consistent with a history of valvular repair with normal gradients and trace residual MR. There is a trivial circumferential pericardial effusion without signs of tamponade physiology. The IVC appearance is consistent with normal RA pressures (0-5 mmHg).
Aktuelle Erkrankungen: N/A
Vorgeschichte: HTN, lyme, mitral valve repair
Andere Medikamente: acetaminophen, aspirin, omeprazole,
Allergien: no known allergies
Vorherige Impfungen: -

VAERS 2084844

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: -
Alter: -
Geschlecht: F
Eingang: 03.02.2022
Impfdatum: 01.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: OT / -

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

Insomnia Rash Rhinorrhoea Thrombosis

Symptomtext

SEVERE BLOOD CLOT IN EYE; SLEEPING DIFFICULTY; LOT OF MUCUS; SEVERE RASH ON NECK WHICH WENT DOWN THE ARMS TO THE ELBOW/RASH ON BACK AND PART OF THE HEAD; This spontaneous report received from a patient concerned a 7 decade old female of unspecified race and ethnicity. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (dose number in series: 1) (suspension for injection, route of admin, and batch number were not reported) dose was not reported, 1 total administered on MAR-2021 for prophylactic vaccination. The batch number was not reported. The Company is unable to perform follow-up to request batch/lot numbers. No concomitant medications were reported. On an unspecified date, following vaccination with covid-19 vaccine ad26.cov2.s, the patient developed a severe blood clot in the eye and a severe rash on the neck which went down the arms to the elbow. The patient had visited the dermatologist and had started to get better. The rash had lasted for several months. The patient also had difficulty sleeping (dose number in series: 1). The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The outcome of the severe blood clot in her eye, severe rash on neck which went down the arms to the elbow/rash on back and part of the head, and sleeping difficulty was not reported. On 10-NOV-2021, the patient received booster of non-company suspect vaccine MRNA 1273 (dose number in series: 2) (form of admin, and route of admin, were not reported, batch number: 033F21A expiry: UNKNOWN) dose was not reported, administered to the left arm shoulder deltoid muscle for prophylactic vaccination. On an unspecified date, following vaccination with MRNA 1273, the patient developed a rash on the back, neck and part of the head. The patient had seen the doctor for the rash and was prescribed with cortisone tablets, antihistamine, ointments and liquids to put on the rash. The patient was also prescribed with clobetasol propionate (Clobetasol 0.05%). The patient also noticed a lot of mucus after the booster vaccine and stated that the rash was not as severe as it was after the covid-19 vaccine ad26.cov2.s. (Dose number in series: 2). The outcome of the lot of mucus was not reported. This report was serious (Other Medically Important Condition).; Sender's Comments: V0: 20220152554 COVID-19 VACCINE AD26.COV2.S- severe blood clot in her eye. This event(s) is considered unassessable. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There is no information on any other factors potentially associated with the event(s).

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

VAERS 2044618

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: NH
Alter: 65,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 07.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / -

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

Loss of consciousness Seizure Tongue biting Tremor

Symptomtext

Note: The pt was lying on her back, shaking, and biting her tongue. She was rolled to her side. The APRN on site came to evaluate the patient. APRN, came up to examine pt. Ativan orders and administered seizure activity occurred at 10:45. Ativan was administered at 11:05. Pt opened their eyes and became conscious at 11:20.

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Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Aphasia Dysphagia Essential Hypertension Rheumatoid Arthritis Fibromyalgia Cerebral Arteritis Barretts Esophagus
Andere Medikamente: -
Allergien: Methotrexate Oxycodone
Vorherige Impfungen: -

VAERS 2024655

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

schwer

Staat: KY
Alter: 63,0
Geschlecht: F
Eingang: 11.01.2022
Impfdatum: 29.12.2020
Beginn: 18.06.2021
Tage bis Beginn: 171,0
Dosis: 3
Route/Site: IM / LA

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

Aspiration pleural cavity Biopsy Biopsy bone marrow Central venous catheterisation Chemotherapy Chest tube insertion Dizziness Dyspnoea Non-Hodgkin's lymphoma Pneumothorax Positron emission tomogram Pulmonary oedema Spinal pain

Symptomtext

I developed a non-hodkins lymphoma. Was hospitalized on June 20, 2021 and a biopsy was completed that week. I have completed 6 months of chemo and immunotherapies. The cancer was wrapped around the aorta and I was short of breath because of fluid in my lungs as well as lightheaded/dizzy. Severe pain in my thoracic spine as well. This was six months after my first injection. Not sure it has any relationship to the vaccine but was recommended by your person who called to submit a report.

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Praegender Schweregrund: Pulmonary oedema
Hospital-Tage: 6,0
Labordaten: biopsy June 24, 2021, thoracentesis June 24, 2021, Chest tube placement for pneumothorax, thoracentesis August 24 2021.. Pet scans x3, Bone marrow biopsy July 14, 2021, Placement of mediport for chemotherapy July 16, 2021.
Aktuelle Erkrankungen: none
Vorgeschichte: arthritis acid reflux
Andere Medikamente: synthroid, hctz, lisinopril, robaxin, protonix, celexa, potassium, tylenol or ibuprofen as needed for pain
Allergien: wellbutrin, biaxin
Vorherige Impfungen: -

VAERS 2012967

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: GA
Alter: 38,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 18.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Arthritis Asthenia Chest X-ray Condition aggravated Dizziness Dizziness postural Dyspnoea exertional Eating disorder Electric shock sensation Electrocardiogram abnormal Fatigue Fine motor skill dysfunction Headache Heavy menstrual bleeding Hypoaesthesia Insomnia Menstrual disorder Nausea

Symptomtext

Dizziness and giddiness (began shortly after 1st dose 10/21/21 and I continue to experience it daily; symptoms enhanced when picking things up off floor or when sitting down); Abnormal EKG (12/16/21) - seeing cardiologist on 2/1/2022 for further testing; Dysnea on exertion; Headaches; Nausea (intermittent Moderate occurrences since 2nd dose); Neck pain on right side; Paresthesia of upper limb (right arm & hand; began 11/21/21; intermittent feelings of shocking/tingling/numbness have intensified since 12/23/21; negatively effects fine motor skills at times); Unusual tiredness and weakness; Significant increase in TMJ pain on right side only (now impacts my ability to eat, talk and sleep; dentist said likely due to inflammation); Changes in Menstrual Cycle (began after first dose; now pass blood clots size of marble to size of quarter)

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Praegender Schweregrund: Electric shock sensation
Hospital-Tage: -
Labordaten: EKG; XR chest 2 view; XR cervical spine 4 or 5 v - all occurred 12/16/21
Aktuelle Erkrankungen: None
Vorgeschichte: -
Andere Medikamente: -
Allergien: None
Vorherige Impfungen: -

VAERS 2006499

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: MA
Alter: 24,0
Geschlecht: M
Eingang: 05.01.2022
Impfdatum: 27.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Chest pain Myocarditis

Symptomtext

Patient was diagnosed with Myocarditis as a result of the booster. Symptoms of chest pain showed up 3 days after the vaccine. The patient was released after a day in the hospital. He was prescribed anti-inflammatories to help with the inflammation. Ongoing check-ins are needed.

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Praegender Schweregrund: Myocarditis
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1972257

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: IL
Alter: 54,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 03.12.2021
Beginn: 11.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / RA

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

Angiogram Bell's palsy Blood magnesium Computerised tomogram abnormal Dyskinesia Eyelid disorder Facial paralysis Feeling abnormal Full blood count Headache Hypoaesthesia oral Lacrimation increased Metabolic function test Musculoskeletal stiffness Neck pain Sleep disorder Speech disorder

Symptomtext

Stiff neck Dec 11, 2021, Very stiff neck Dec 12, 2021. Awakened by Severe neck and head Pain at 1:47 am Dec 13, 2021 pain prevented sleeping, used about 8 200mg ibuprofen to deal with pain until going to Chiropractor @ 5PM Dec 13, 2021. Chiropractic adjustment relieved some of pain. About an hour later I felt numbness in upper lip. Woke up about 4 am Dec 14, 2021 with watering right eye, and pain right side of head near ear, face felt strange, didn't seem to work correctly. Went to get a drink of water and it ran down my face. Noticed right side of my face drooping, Right eye not shutting, lips not working correctly. Left a message with Dr. office that morning. They instructed me to go to Emergency Room. Got to E.R. around 11:45 am. By then I had difficulty speaking properly. had blood drawn, physical exam, C.T. scan, Diagnosed with Bell's Palsy

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: CBC WITH DIFFERENTIAL COMPREHENSIVE METABOLIC PANEL MAGNESIUM CT ANGIO HEAD & NECK Iopamidol (Isovue-370) 76 % injection 100 mL Last given at 3:39 PM
Aktuelle Erkrankungen: None
Vorgeschichte: Knee pain: right has chonromalacia, // Shoulder pain-2006 left shoulder pain due to being hit by a truck at work
Andere Medikamente: Puritan's Pride-Ultra Man 50 plus daily multi-vitamin, L-theanine 300mg, 5-HTP 200mg, GABA 750mg // Osteo Bi-Flex Joint Health Triple Strength // Wonder Labs: Melatonin 2.5mg sublingual // Alprazolam as needed
Allergien: None
Vorherige Impfungen: -

VAERS 1963589

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: VA
Alter: 43,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 11.11.2021
Beginn: 03.12.2021
Tage bis Beginn: 22,0
Dosis: 3
Route/Site: SYR / LA

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

Blood iron abnormal Coagulation factor VIII level increased Dizziness Fatigue Feeling abnormal Interchange of vaccine products Loss of consciousness Unresponsive to stimuli Von Willebrand's factor activity increased

Symptomtext

I had my covid booster on November 11. I had Pfizer the first two doses and chose the Moderna booster. On December 3, at a previously scheduled specialist doctor's appointment, I had blood work drawn related to the appointment. Felt a bit lightheaded after blood draw and nurse left room to get juice. She returned and I was nonresponsive ... was out for about a minute and took some time to feel normal again. For most of 'Saturday was still incredibly fatigued. I have blood work regularly for my thyroid checks and have done other fasting blood work and never reacted like this. I was doing a smartphone based check in after the event and reported seeking care and having a reaction and was called by the app administrator and given this website and told I could make a report, or not. My choice. I have no idea if my reaction that day was in any way related to my booster or vaccine series or if it was totally in isolation. It was three weeks after the booster dose was administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: No tests were done related to the event, but blood work had just been drawn prior to the episode ... iron levels were off (and had been normal in September) ... without other changes to diet, etc. Also, VON WILLEBRAND RISTOCETIN COFACTOR (VWF) ACTIVITY and Factor VIII were both elevated, but I don't think have ever been checked before ... so, again, probably totally unrelated, but just mentioning since asked.
Aktuelle Erkrankungen: none known
Vorgeschichte: history of thyroid cancer Currently being screened for some other issues
Andere Medikamente: I take thyroid hormone replacement daily due to total thyroidectomy for thyroid cancer in 2012. I also take Vitamin D daily and sometimes multi or vitamin c.
Allergien: allergic to gluten
Vorherige Impfungen: Reacted to flu vaccine in 2018. The site of the injection became red, hard, painful, and swollen and itched severely for several

VAERS 1961408

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

schwer

Staat: NY
Alter: 28,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 02.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: SYR / -

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

Heavy menstrual bleeding Lymph node pain Lymphadenopathy Swelling of eyelid Thrombosis

Symptomtext

Left. Eyelid swelling Left facial Lymph node pain and swelling from temple to check 13 day heavy menstruation. Multiple clots per hour of every single day

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Praegender Schweregrund: Thrombosis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hidradenitis supparativa
Andere Medikamente: Humira Vitamin D
Allergien: Fish
Vorherige Impfungen: -

VAERS 1954839

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: MD
Alter: 48,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 09.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Facial paralysis Headache

Symptomtext

Received Covid Booster/Moderna on 12/09/2021 in the morning, after 5 hours, the patient developed headache 8/10, from the frontal lobe back to the occiput. No prior history of headaches/migraines. The headache has been pressure like since for "24/7", not relieved by tylenol or ibuprofen.

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Praegender Schweregrund: Facial paralysis
Hospital-Tage: -
Labordaten: Evaluated by Medical Health on 12/16/2021, was sent to Emergency Room for further evaluation of h/a and right facial droop. r/o stroke.
Aktuelle Erkrankungen: none
Vorgeschichte: arrhythmia, PVCs, Gastric Bypass 2015
Andere Medikamente: effexor, amlodipine, metoprolol, tumeric, vit B12 injections, vitamin D
Allergien: Penicillin, Codeine, Sulfa, Robinul
Vorherige Impfungen: -

VAERS 1931902

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21A

schwer

Staat: CT
Alter: 48,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 05.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Dyspnoea Fall Flushing Hyperhidrosis Loss of consciousness Visual impairment

Symptomtext

Systemic: Allergic: Difficulty Breathing-Medium, Systemic: Dizziness / Lightheadness-Medium, Systemic: Flushed / Sweating-Medium, Systemic: Visual Changes/Disturbances-Medium, Additional Details: pt during 15min wait time after booster vaccine, becomes dizzy, falls 6-8 mins after adminsitration. sweating profusely, complained could not breath, administered epinphrine at this point. blacking out, seeing stars. remained conscious throught. called 911 when pt blacking out. girlfriend recieved 30min before pt, says pt might have psyched self out. recieved moderna 1/2 dose no issues.

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

VAERS 1920943

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: NY
Alter: 25,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 02.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Contusion Fall Head injury Injection site pain Syncope

Symptomtext

Pt work with chills and pain at injection site and suffered a vasovagal syncopal episode while attempting to get Advil from bathroom, she fell and hit her head, suffering a contusion. At time of office visit the following morning, she does not appear to have signs of concussion or more serious head or neck injury.

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

VAERS 1919271

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: TX
Alter: 74,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 02.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 7,0
Dosis: UNK
Route/Site: IM / LA

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

Asthenia Full blood count Gait inability Guillain-Barre syndrome Lumbar puncture Magnetic resonance imaging spinal Myalgia Pain in extremity Paraesthesia Paralysis

Symptomtext

11/09/2021 patient felt muscle aches, tingling on hands and feet, 11/16/2021 rush her to hospital because of severe pain on both upper and lower extremities, admitted at hospital until 11/17/2021, readmitted on 11/20/2021 because patient cannot walk anymore, due to weakeness/paralysis. Diagnosed for Guillane barre syndrome from Moderna booster shot she got on 11/02/2021

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Praegender Schweregrund: Guillain-Barre syndrome
Hospital-Tage: 8,0
Labordaten: MRI of spine, Lumbar tap, CBC
Aktuelle Erkrankungen: none
Vorgeschichte: asthma
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1912656

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: KY
Alter: 36,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 10.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Bell's palsy Condition aggravated Facial paralysis

Symptomtext

Friday 11/12/2021 at approximate 3:30PM- patient noted facial drooping. Seen at ED by ED physician. Dx Bell's Palsy and steroids prescribed. Patients states has had Bell's Palsy in past.

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Praegender Schweregrund: Bell's palsy
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1902190

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: MA
Alter: 19,0
Geschlecht: F
Eingang: 26.11.2021
Impfdatum: 24.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Syncope Vomiting

Symptomtext

Syncope and vomiting at 10 am 11/25 after receiving booster at 7 pmOn 11/24. Second heat syncope incident at 5 pm same day (11/25), but she had barely eaten all day. No vomiting second time and once syncope was over, ate normally, sipped Gatorade and lemonade and has been fine since. Taking Extra Strength Tylenol every 4 hrs. Has been fine all day 11/26 but continuing Tylenol today as a precaution.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: mild asthma, typically only triggered by exercise or upper respiratory infections
Andere Medikamente: Zoloft
Allergien: Shellfish allergy
Vorherige Impfungen: -

VAERS 1901585

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: KS
Alter: 67,0
Geschlecht: F
Eingang: 26.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Asthenia Chest pain Chills Condition aggravated Dyspnoea Fear Headache Inflammation Musculoskeletal stiffness Nausea Pericarditis Pyrexia

Symptomtext

May have experienced pericarditis; Stiff neck; Shooting pains in her chest/pain deep in chest/chest pains are better but "still at bay"/chest pains are now just a dull ache/no longer a severe, sharp burning pain in the chest.; Shortness of breath; Scary; Severe inflammation; Got worse when she laid down//went to bed; too weak last night to do anything; Nausea; Fever; Chills; Headache/shooting pains in her head; This spontaneous case was reported by a consumer and describes the occurrence of PERICARDITIS (May have experienced pericarditis) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Sulfonamide allergy (drug allergy to sulfa and gluten), Hashimoto's disease (Hashimoto's disease and she treats with a compounded T3/T4 medication.) and Gluten sensitivity. Concomitant products included T3/T4 SUPPORT for Hashimoto's disease. On 18-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Nov-2021, the patient experienced PERICARDITIS (May have experienced pericarditis) (seriousness criterion medically significant), MUSCULOSKELETAL STIFFNESS (Stiff neck), CHEST PAIN (Shooting pains in her chest/pain deep in chest/chest pains are better but "still at bay"/chest pains are now just a dull ache/no longer a severe, sharp burning pain in the chest.), DYSPNOEA (Shortness of breath), FEAR (Scary), INFLAMMATION (Severe inflammation), CONDITION AGGRAVATED (Got worse when she laid down//went to bed), ASTHENIA (too weak last night to do anything), NAUSEA (Nausea), PYREXIA (Fever), CHILLS (Chills) and HEADACHE (Headache/shooting pains in her head). The patient was treated with IBUPROFEN 19-Nov-2021 for Chest pain, at a dose of 1 dosage form three times a day and ACETAMINOPHEN on 19-Nov-2021 at a dose of 1 dosage form. At the time of the report, PERICARDITIS (May have experienced pericarditis), MUSCULOSKELETAL STIFFNESS (Stiff neck), DYSPNOEA (Shortness of breath), FEAR (Scary), INFLAMMATION (Severe inflammation), CONDITION AGGRAVATED (Got worse when she laid down//went to bed), ASTHENIA (too weak last night to do anything), NAUSEA (Nausea), PYREXIA (Fever), CHILLS (Chills) and HEADACHE (Headache/shooting pains in her head) outcome was unknown and CHEST PAIN (Shooting pains in her chest/pain deep in chest/chest pains are better but "still at bay"/chest pains are now just a dull ache/no longer a severe, sharp burning pain in the chest.) was resolving. Company Comment: This is a spontaneous case concerning a 67 years old, female patient with clinical history of Hashimoto's disease who experienced the expected event of PERICARDITIS (AESI) and the unexpected events of MUSCULOSKELETAL STIFFNESS, CHEST PAIN, DYSPNOEA, FEAR, INFLAMMATION, CONDITION AGGRAVATED, ASTHENIA, NAUSEA, PYREXIA, CHILLS and HEADACHE. The events occurred the same day after the third dose of mRNA-1273 vaccine. The rechallenge was not applicable since only information about the third dose was disclosed. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This is a spontaneous case concerning a 67 years old, female patient with clinical history of Hashimoto's disease who experienced the expected event of PERICARDITIS (AESI) and the unexpected events of MUSCULOSKELETAL STIFFNESS, CHEST PAIN, DYSPNOEA, FEAR, INFLAMMATION, CONDITION AGGRAVATED, ASTHENIA, NAUSEA, PYREXIA, CHILLS and HEADACHE The events occurred the same day after the third dose of mRNA-1273 vaccine The rechallenge was not applicable since only information about the third dose was disclosed The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pericarditis
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Gluten sensitivity; Hashimoto's disease (Hashimoto's disease and she treats with a compounded T3/T4 medication.); Sulfonamide allergy (drug allergy to sulfa and gluten)
Vorgeschichte: -
Andere Medikamente: T3/T4 SUPPORT
Allergien: -
Vorherige Impfungen: -

VAERS 1894167

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: CT
Alter: 25,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 23.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / -

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

Dizziness Seizure

Symptomtext

Patient started to feel lightheaded and convulsed. He eventually slid down his chair and was caught by his parent. Our medical presiding Doctor tended to him and he felt better after some time with water and a snack bar. The ambulance came and he felt better at the moment and refused to go with them. Parents were with him and will be driving him to get his bloodwork done for further screening.

Weitere VAERSDATA-Felder

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

VAERS 1886451

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: MT
Alter: 62,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Chills Extra dose administered Headache Nausea Palpitations Pharyngeal swelling Presyncope

Symptomtext

Heart palpitations, close to fainting (room appeared getting dark), swelling sensation in throat, severe headache, nausea, chills. Symptoms began 12 minutes after receiving the COVID-19 Moderna booster. 50 cc?s of liquid benedryl was given as treatment as well as kept me in the urgent care to monitor my heart rhythm and oxygen level for approximately two and a half hours. Then discharged.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Presyncope
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Strep
Vorgeschichte: Chronic Arthiritis, asthma, compromised immune system
Andere Medikamente: Zertec, Omeprozole, Folic Acid, Vitamin D
Allergien: Codeine, tetracycline, phenergen,
Vorherige Impfungen: -

VAERS 1885656

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: HI
Alter: 57,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 05.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal discomfort Chills Diarrhoea Impaired work ability Pyrexia Syncope Vomiting

Symptomtext

Sunday morning, started with upset stomach and then diarrhea. Later, vomiting's and continuous diarrhea (like liquids) throughout the night. Fever up to 101.7, chills and fainted. Eventually after 48 hrs. since the booster shot, I finally took some Tylenol and helped brought down fever, which eventually made me feel better. Diarrhea started to slow down by Tuesday. Went back to work on Wednesday but stomach was still not all well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: did not see doctor
Aktuelle Erkrankungen: none
Vorgeschichte: Mitral valve prolapse; high blood pressure; high cholestorol
Andere Medikamente: Hydrochlorothiazide 25 mg; Atorvastatin Calcium 40 mg; Citracal 1890mg; fish oil 2000 mg; super B-complex 1 tablet; D3 4000 IU; Nutrafol 4 tablets.
Allergien: n/a
Vorherige Impfungen: -

VAERS 1876229

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: TX
Alter: 31,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Mild, Additional Details: Patient received Booster Dose of Moderna after receiving J&J as first dose. Patient fainted in waiting area while seated approximately 10 minutes after the injection. Patient revived on her own and was helped to a sitting postion on the floor. She did not complain of any pain or injury and fully recovered and was escorted home by her husband.

Weitere VAERSDATA-Felder

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

VAERS 1861623

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: TX
Alter: 26,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 05.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain upper Activated partial thromboplastin time Blood test C-reactive protein Cardiac monitoring Blood creatine phosphokinase increased Chest pain Chills Diarrhoea Echocardiogram normal Chest X-ray abnormal Echocardiogram Electrocardiogram Electrocardiogram abnormal Full blood count Headache Human chorionic gonadotropin Inflammation

Symptomtext

Moderna COVID-19 Vaccine EUA: Pericarditis / Myocarditis Patient with latent TB s/p 9 mths INH tx with persistent GI symptoms, received Moderna Vaccines on 3/3/2021, 3/31/2021, and 11/05/2021. On 11/6/2021 patient began to have chills, fatigue, & fever as high as 101.0. Early on the morning of 11/8/2021 around 2 a.m. she began diarrhea, vomitiing and chest pain which was made worse by lying down. Persistent fevers as well as sweats prompted to come to the ER. EKG was abnormal (diffuse ST elevation), echocardiogram obtained which was stable. Patient began to improve over the next few hours and was discharged in stable condition on 11/9/2021. Covid test negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 1,0
Labordaten: Troponin I: 2531 on 11/8 @ 0507, 6266 on 11/8 @ 0910, 2762 on 11/9 @ 0406. Virus panels all negative. Creatine kinase 221 on 11/8 @ 0507
Aktuelle Erkrankungen: -
Vorgeschichte: Latent TB in 2019
Andere Medikamente: Cetirizine QD prn, Fluticasone Nasal QD, Montelukast 10 mg QD, Loestrin 1.5/30 QD, Omeprazole 40 mg QD.
Allergien: Doxycycline (itch / rash)
Vorherige Impfungen: -

VAERS 1861623

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: TX
Alter: 26,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 05.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain upper Activated partial thromboplastin time Blood test C-reactive protein Cardiac monitoring Blood creatine phosphokinase increased Chest pain Chills Diarrhoea Echocardiogram normal Chest X-ray abnormal Echocardiogram Electrocardiogram Electrocardiogram abnormal Full blood count Headache Human chorionic gonadotropin Inflammation

Symptomtext

Moderna COVID-19 Vaccine EUA: Pericarditis / Myocarditis Patient with latent TB s/p 9 mths INH tx with persistent GI symptoms, received Moderna Vaccines on 3/3/2021, 3/31/2021, and 11/05/2021. On 11/6/2021 patient began to have chills, fatigue, & fever as high as 101.0. Early on the morning of 11/8/2021 around 2 a.m. she began diarrhea, vomitiing and chest pain which was made worse by lying down. Persistent fevers as well as sweats prompted to come to the ER. EKG was abnormal (diffuse ST elevation), echocardiogram obtained which was stable. Patient began to improve over the next few hours and was discharged in stable condition on 11/9/2021. Covid test negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myocarditis
Hospital-Tage: 1,0
Labordaten: Troponin I: 2531 on 11/8 @ 0507, 6266 on 11/8 @ 0910, 2762 on 11/9 @ 0406. Virus panels all negative. Creatine kinase 221 on 11/8 @ 0507
Aktuelle Erkrankungen: -
Vorgeschichte: Latent TB in 2019
Andere Medikamente: Cetirizine QD prn, Fluticasone Nasal QD, Montelukast 10 mg QD, Loestrin 1.5/30 QD, Omeprazole 40 mg QD.
Allergien: Doxycycline (itch / rash)
Vorherige Impfungen: -

VAERS 1864530

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: KS
Alter: 32,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Dizziness Fatigue Injection site bruising Lethargy Syncope Unresponsive to stimuli Vomiting

Symptomtext

Site: Bruising at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Vomiting-Mild, Systemic: Weakness-Mild, Additional Details: EMT/EMS called and patient had caregiver come pick him up

Weitere VAERSDATA-Felder

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

VAERS 1864510

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

schwer

Staat: OH
Alter: 23,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Fall Flushing Hyperhidrosis Syncope Unresponsive to stimuli

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Systemic: Fainting / Unresponsive-Medium, Systemic: Flushed / Sweating-Medium, Additional Details: Patient received first covid vaccine dose - no allergies - does not routinely get vaccinated but was not nervous per patient - about 5 minutes after his dose he felt faint and fell down quickly he needed water and was sweating. Patient began to feel better but had the EMS check him out anyways and escort him out after a waiting period to make sure he was ok. His BP was normal.

Weitere VAERSDATA-Felder

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

VAERS 1860503

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

schwer

Staat: CA
Alter: 29,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness Seizure Unresponsive to stimuli Visual impairment

Symptomtext

approx 5-10 mins after receiving the vaccine patient reported dizziness, light headedness, and seeing spots. nurse administering had patient lie down with legs up and checked vital signs. patient did not report anaphylactic type reaction so epipen was not given, but held ready in case. about 30 mins after dose, patient reported feeling better and sat up in a chair. after additional 2-5 mins patient was not responding to verbal cues and appeared unable to speak or move despite appearing awake. nurse and NP in store suspected seizure. ambulance was called and all vital signs continued to be monitored

Weitere VAERSDATA-Felder

Praegender Schweregrund: Seizure
Hospital-Tage: -
Labordaten: all tests on 11/10/21, vitals including BP, pulse, and breathing were documented every 5-10 mins. BP recorded 111/89 , 112/75, 106/74, pulse recorded at 68, 67 , 67
Aktuelle Erkrankungen: none noted
Vorgeschichte: none noted on form, nurse administering vaccine said patient indicated she had a tic-like condition i.e. tourette's syndrome, and had an adverse reaction (anaphylaxis) to Johnson and Johnson Covid Vaccine
Andere Medikamente: unknown, patient does not regularly receive medication from this pharmacy, patient unable to provide details after event / before paramedics arrived
Allergien: strawberry, apple, cherry, bee pollen, cat hair
Vorherige Impfungen: Johnson and Johnson covid vaccine, patient reported anaphylactic type reaction, though this was not independently verified

VAERS 1850604

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: NY
Alter: 50,0
Geschlecht: M
Eingang: 08.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Amnesia Balance disorder Hypoaesthesia Loss of consciousness

Symptomtext

On 11/5, I recieved the Maderna Shot at location. On Saturday morning, my left leg and foot was numb same as the first shot. It is 11/8 the numbness remains. Also, my equilibrium is off, and I have slight memory loss or momentary blackouts. For example, since the 1st dose, I have been intending to do something such as opening the refrigerator to get a drink then, forgeting what I opened the refrigerator for. I have since been wearing Orthapedic Shoes to promote circulation, and ride my bike to sustain strength in my legs. With regards to the blackouts, I am playing brain teasers to see where I am on a daily basis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: None have been taken because no one is documenting anything.
Aktuelle Erkrankungen: None.
Vorgeschichte: None.
Andere Medikamente: None.
Allergien: None.
Vorherige Impfungen: Stomach Ache, 48 years, 12/9/2019, Flu Shot

VAERS 1848685

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

schwer

Staat: MA
Alter: 59,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Anaphylactic reaction Dyspnoea

Symptomtext

Systemic: Allergic: Anaphylaxis-Severe, Systemic: Allergic: Difficulty Breathing-Severe

Weitere VAERSDATA-Felder

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

VAERS 1845899

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: NJ
Alter: 30,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Altered state of consciousness Asthenia Balance disorder Blindness transient Disorientation Dizziness Fall Fatigue Flushing Hallucination Headache Heart rate abnormal Hyperhidrosis Hypoaesthesia Hypotension Hypoxia Immobile Loss of consciousness

Symptomtext

Summary: Hypoxemia, loss of consciousness, altered consciousness, tachycardia. Lowest measured blood o2 was 85% after substantial improvement in symptoms. So blood o2 could have been even lower earlier in the event. See these unedited notes from the event that I took: In hindsight: Awoke on floor. Location unknown. Ejected out of bed launching weight blanket across the room. Dizziness and hallucinations to the point of incapacitated. Static feeling skin, face numb, could not see surroundings but saw gently moving white auras and shapes that disoriented. Symptoms worse lifting head up, altered consciousness. Loss of consciousness if symptoms progressed. Disorientation and vision returned with immobility, sense of touch returned predominately feeling tachycardia throughout body. Fingers and feet static but pulse. Made it back to side of bed and collected phone at 11:55 recall seeing the time, but phone record shows it was actually 11:23. Vision returned but distorted, found the phone by its cold touch. Got back into bed, immobility helps. Tachycardia, no increased respiration. Symptoms returned trying to sit up. Took an ibuprofen 200 with water. 00:15 wrote the above this sweating but can make sense of surroundings. Sensation similar to hypovolumeia. Suspect hypotension. 00:21. Feeling much better, find oximeter. Pulse 132 O2 86% 85%. Fingers warmed by heating pad. Different hands. Now Manually doing big gentle breathes periodically. Can compute mental math. Another ibu 200 with water. Can't accurately measure respiratory rate but seems normal. Sensation of pulse persists through body, ankles and ears. Sweating. Low grade headache 0027 102 bpm 92% o2. Use of albuterol hfa without symptoms of breathing problems. Balance problems when walking, surroundings shift mildly. Sense of touch works. Resolve upon laying down. 0034 97% 90 bpm oh shit moment of the severity of low o2 0035 96% 95bpm 0044 97% 97bpm 0056 97% 97 bpm. Flushing subsides. Headache still present. Very tired but way too keyed up. 0052 95% 101 0105 98% 90 no disorientation on sitting up. Feel fine apart from heart rate, a little headache, and tiredness 0119 97% 88. Brief lightheadedness standing up. Vision edge distortion. Resolved in seconds 0143 98% 88bpm. Fell asleep until 0744 0744 98 65bpm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Loss of consciousness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Male to female transgender
Andere Medikamente: Estradiol Valerate IM same deltoid Cyproterone Acetate 2mg po qd Multivitamin with dha Vitamin d
Allergien: Macrolids
Vorherige Impfungen: General reactogenity to vaccines. Sore chest, pain in joints, low fever

VAERS 1839880

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

schwer

Staat: NC
Alter: 21,0
Geschlecht: M
Eingang: 03.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Hyperhidrosis Loss of consciousness

Symptomtext

Patient passed out 10 mins after receiving vaccine. Pharmacist stated that 911 was called, also said patient was sweating profusely.

Weitere VAERSDATA-Felder

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

VAERS 1837406

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21A

schwer

Staat: NJ
Alter: 25,0
Geschlecht: M
Eingang: 02.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Condition aggravated Fall Skin laceration Syncope Tooth fracture

Symptomtext

Patient fainted and had appeared to seize for approx 1 minute at 0614. Fall from chair resulted in laceration of chin and chipped tooth. Ambulance called and pt taken in for evaluation by stretcher. BP stable 133/84

Weitere VAERSDATA-Felder

Praegender Schweregrund: Syncope
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Patient says he has history of fainting at site of blood, unsure of history of seizures. Has not sought medical attention for syncope in the past
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1836918

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

schwer

Staat: MA
Alter: 19,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Loss of consciousness Syncope Unresponsive to stimuli

Symptomtext

Systemic: Fainting / Unresponsive-Medium, Additional Details: pt passed out and hit head on glass screen behind chair then woke up in a few minutes completely responsive afterwards.

Weitere VAERSDATA-Felder

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

VAERS 1836903

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

schwer

Staat: MA
Alter: 50,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Adverse reaction Confusional state Disorientation Dizziness Flushing Hyperhidrosis Hypotension Loss of consciousness Pulse absent Syncope Unresponsive to stimuli

Symptomtext

Systemic: Confusion-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Hypotension-Severe, Additional Details: Called EMS after patient was identified having adverse effects. Moved patient to ground to lay down. Could not find a pulse. After a few seconds patient regained consciousness, but was still very confused and disoriented. Instructed patient to ramain supine until EMS arrived. No s/s of allergic rxn. Hypotensive. Patient was taken out of store via stretcher & ambulance. I am unsure of outcome.

Weitere VAERSDATA-Felder

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

VAERS 2548062

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: IL
Alter: 78,0
Geschlecht: F
Eingang: 02.01.2023
Impfdatum: 29.12.2021
Beginn: 09.01.2022
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

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

Cardiac disorder Cardiac stress test Catheterisation cardiac Computerised tomogram thorax Dyspnoea Electrocardiogram Pulmonary function test Scan abnormal Scan with contrast Stent placement

Symptomtext

1 month after the booster I woke up and could not breathe. I had several scans and eventually had to have a stent implanted and was placed on oxygen and several new medicines which I never needed prior to this booster. I was prescribed several new medicines afterward as follows: Bumex 0.5-1.0 mg, Montelukast 10 mg, Carvedilol 3.124 mg, Entrtesto 49/51 mg, Plavix 75 mg, Jardiance 10 mg

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Complete PFT W + WP BRONCHODILATOR 10/10/22 ; INTERVENTIONAL CATH PROCEDURE 8/5/22; VPOD OVERNIGHT OXIMETRY; CVC LHC LEFT HEART CATH 7/22/22; CT CARDIAC W/CONTRAST 7/19/22; CT CHEST W/CONTRAST 6/29/22; STRESS TEST 3/29/22; EKG 2/23/22
Aktuelle Erkrankungen: None
Vorgeschichte: Sleep apnea, diabetes type 2, high blood pressure, trigeminal neuralgia Since I took the booster of ModernaCovid -19 Lot 033F21A on 12/9/21, beginning 1/9/22 I have had breathing issues and heart issues which I did not have prior to that. In Dec. 2021 all my blood labs were perfect and my doctor said my health was above average for my age. After that on Jan. 9, 2022 I woke up and could not breathe. I had to have a stent implanted and was prescribed 2ml of oxygen at night. I didn't have any of this issue before the booster.
Andere Medikamente: Certizine 10 mg, Gabapentin 100-300 mg, Glipizidre 2.5 mg, Furosemide 40 mg, Losartan 100 mg, Mucinex 1000 mg, Atorvastatin 20 mg, Famotidine 40 mg, Levothyroxine 112.mcg, Omeprazole 20 mg, Metformin 2000 mg, L-Lysine 500-1200 mg, Calcium
Allergien: Alli, Tenuate Dosopan, paper tape, Fentanyl
Vorherige Impfungen: -

VAERS 2524305

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: VA
Alter: 27,0
Geschlecht: F
Eingang: 06.12.2022
Impfdatum: 03.12.2021
Beginn: 15.09.2022
Tage bis Beginn: 286,0
Dosis: 3
Route/Site: SYR / LA

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

Computerised tomogram normal Headache Migraine

Symptomtext

I experienced and have been, ongoing migraines since the day I had an acute migraine attack that put me in the hospital. Everyday I've been having headaches. I was put on 2 different steroids.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: CT scan normal
Aktuelle Erkrankungen: No
Vorgeschichte: Anxiety
Andere Medikamente: Sertraline; JUNEL
Allergien: No
Vorherige Impfungen: -

VAERS 2475545

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: NH
Alter: 32,0
Geschlecht: F
Eingang: 11.10.2022
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Agoraphobia Akathisia Alopecia Anxiety Arrhythmia Autoimmune disorder Blood pressure increased Blood test normal Borrelia test COVID-19 Cardiac monitoring abnormal Chest X-ray normal Chest discomfort Chest pain Choking sensation Computerised tomogram head normal Dental discomfort Depersonalisation/derealisation disorder

Symptomtext

Symptoms: Feeling of pressure in head that usually pulsates to the beat of my heart Ear pressure and extreme tinnitus PVC?s (pre ventricle contractions - heart skipping beats or ?backfiring?) Palpitations Chest Pressure and pain - Feeling like I got hit in the chest with a soccer ball. Rushes of what I can best describe as a physical warm anxious energy that starts below both ribs and radiates up over my chest and heart area, down my left arm and sometimes into my neck/jaw, happening right as I?m about to fall asleep. I have these over and over again each night, always as I?m about to bridge the gap between being asleep and awake. I often jump up and sometimes even gasp for air. Most of the time my heart rate seems to stay the same. Once in a while though it will increase. These happen for hours until I?m finally able to fall asleep. It also sometimes coincides with a feeling of being dizzy or like you?re falling backwards. When I jump up from one, I usually have to open my eyes and center myself on the non-moving surroundings to feel stable. These sensations only happen when I?m trying to go to sleep and go away a few seconds after I am alerted by one. I have them every single night and they are usually accompanied by a buzzing sensation and pressure/weighted feeling in my head and chest. Feelings during the day of anxious ?lava? flowing in the area below both ribs. A feeling of extreme anxiety coupled with it. Its not a normal stomach ache or feeling of being nauseous, its what I best describe as that feeling you get when someone startles you or the feeling you get when you show up to class and realize today is the midterm exam you totally forgot about. I can physically feel anxious energy in the area swirling around that is uncomfortable and makes it hard to sit still. It often makes me feel the need to curl into the fetal position to alleviate it (I don?t usually do this, however, it just feels like that is my body?s natural response to handling it). Extreme anxiety/panic attacks and agoraphobia Tightness in throat muscles Feeling of lump in throat or heart beating in throat Hard ?thumping? heart. Not fast but hard. I can?t stand the feeling of it and can no longer sleep on my left side as it feels so loud pounding against my rib and the bed. This often coincides with the head pressure feeling and usually gets worse as the day goes on and isn?t very noticeable first thing in the morning. Sometimes at night if I lie down on the floor to watch a movie and then get up quickly my heart forcefully beats and my head throbs with pressure. Feeling of trouble swallowing food sometimes Chest/arm pressure and heaviness Dizziness that seems most noticeable when I move my eyes from one thing to the other or am scrolling on my phone. This usually feels like my eyes are lagging behind my head. I can no longer sit in the recliners at my house as the movement of them makes me feel unstable and even more dizzy. I had an episode on New Years Eve where I was sitting in the recliner and looked up quickly and all of a sudden my vision just started spinning and flip-flopped. This happened for a few seconds and caused me to panic and immediately check the pulse in my neck. I noticed PVC?s happening and my heart rhythm ?stuttered? and then corrected itself like 5-10 seconds later. I then had a normal panic attack where my heart rate increased rapidly and my blood pressure went up. I was able to get my BP down fairly quickly after this episode but it really shook me up. Loss of hair. I noticed this a month after the second Covid vaccine. Incredible sinus pressure (usually beats to heart as well) and clogged sinuses. I feel as though my nasal passages are swollen to the size of a pin. They often both get so blocked that I can?t breathe out of my nose but don't seemed to be congested. I notice this the most at night. I don?t have a history of any known allergies but I?m starting to wonder. Upper teeth pressure. Often hard to carry on long conversations as I feel a pain/stiffness/pressure feeling in my throat and chest muscles. This sensation is very hard to describe and is accompanied by the head pressure feeling. Weird pains in body - especially upper chest, neck, collar bones, back, head (usually base of skull) and shoulders/upper arms. Neurological pain. Akathisia and inner tremors. These became very intense a few days after the Covid booster. Sometimes it feels like my muscles are writhing inside and I need to move them to make the feelings stop. I feel like I?m shaking on the inside and that they will progress to me having a seizure. That never happens and I usually don?t physically shake externally. Internal buzzing/vibrating/tingling sensation. This sensation is new and very disturbing and is there all the time. Sometimes it is worse than others and seems to get ?louder? when I?m more stressed out. This is most noticeably in my head and chest area as well as my arms. I do feel it everywhere though. This symptom has totally freaked me out. I notice it the most at night. I often feel like I'm plugged into an electrical outlet. Insomnia. I have trouble falling asleep and trouble staying asleep. Inner itching. This one is also hard to describe but it felt as though my brain and face were itching on the inside. Feeling of costochondritis (I?ve never been diagnosed). This comes and goes. Paresthesia Sometimes I can?t laugh hard as it feels like it is putting too much stress on my body and my muscles are tensing up and I will erupt into a seizure. This one is another bizarre symptom, and I know how crazy it sounds. It is also one that is hard to describe. Sensitivities to extreme temps Irregular menstrual cycle after booster. I had my period twice in December. Pulsating (to beat of heart) pressurized choking feeling in throat. Sometimes it feels like all this pressure is building up and there is no way and nowhere to let it out. This is what makes it hard to talk sometimes or feel like I?m choking and that my heart is blocking my airway. It is very hard to lie down when this happens as the heart-smothering feeling intensifies. This sensation makes it feel like it is hard to breathe. Muscle twitching Muscle stiffness and feeling of inability to relax muscles. I often joke when this symptom is present that it feels like I have rigor mortis. Brain fog Vision problems - blurry vision sometimes Depersonalization and derealization Trouble breathing. Feeling like I am unable to get a deep breath Increased blood pressure Timeline: November 19th 2021: Covid Moderna booster at 5:00pm. At midnight I went to the bathroom and felt very dizzy and strange. November 20th 2021: I was lying in bed watching tv when I felt my heart start having PVC?s and ?backfiring? or skipping beats. I felt the pulse in my neck and could feel my heart rhythm was stuttering. I panicked and jumped out of bed. It felt like it took a solid minute before my heart rhythm corrected itself. My heart started beating very fast and I had a severe panic attack. I was on the floor shaking. My blood pressure was elevated to about 145/100 and it took an hour to get it back down to normal. November 22nd 2021: Went to work at 8:00am and had chest pressure/pain and felt like someone had kicked me in the chest with a soccer ball. Had a panic attack and drove myself to the ER where they did an EKG and blood work and said that everything looked fine. The doctor told me he sent the ekg over to a cardiologist for review as well as he always does, just to be sure. When I looked at the EKG in chart that night when I got home, I noticed that it said ?probable left atrial enlargement? at the top. I didn?t understand why they sent me home and told me I was fine. I asked my PCP and she said that the machine interprets the test and writes things in at the top that aren't always accurate. She also reviewed the ekg and told me that it was fine and that my ?p waves look beautiful.? November 26th 2021: Go to the ER for feeling dizzy and chest pain and head pressure. They completed bloodwork, ekg, chest x-ray, urinalysis, CT scan of head, and found nothing. November 28th 2021: Can?t sleep due to intense restless leg feeling and akathisia. November 29th 2021: Call out of work and get in to see my doctor. Begin Short Term Disability. I make a plan with my doctor to try and reinstate a low dose of Lexapro despite my beliefs that these medications have an iatrogenic effect on me. November 30th 2021: Take .5mg of Lexapro for the next 3 days and feel an increase in my symptoms. I stop the medication after 3 days. This is around the time that I notice a new buzzing/tingling/vibrating sensation in my body. My tinnitus has gotten worse now also. December 31st 2021: I?m sitting in the recliner and move my head/eyes and all of a sudden my vision just starts spinning and flip-flops and my heart feels like its rhythm is messing up and skipping beats. This is described in greater detail above in the symptoms section. January 21st 2022: Went to cardiology to have heart monitor put on. This will monitor my heart for 3 days. March 15th: Resting heartrate starts dropping this week. It is usually at about 46-47 but drops suddenly down to 45 for a day then 44 for another day then down to 43 and 42 and stays down in this area. March 18th: Feeling of breathlessness begins. Feeling like I can?t get a satisfying breath in. End of March: Go to the ER twice in a week for feelings of breathlessness. April 5th: Diagnosed with autoimmune disease that affects dopamine receptors and blood brain barrier disruption,as well as antibodies to lyme and two types of EBV. May 10th : Mom tests positive for Covid. I have symptoms. Tickle in throat that progresses to feelings of being unwell. I can tell I am getting sick. May 12th: Test positive for Covid. Develop a significant increase in PVC?s. Go to the ER. May 27th-29th: Wore Ziopatch heart monitor. June 8th: Get results from heart monitor back. This shows a significant increase in ectopic heartbeats :premature beat originating in the lower chambers).

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Praegender Schweregrund: Arrhythmia
Hospital-Tage: -
Labordaten: Heart Monitor EKG I have to have an ablation in November to fix my new heart arrhythmia
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Magnesium, L-Theanine, Valerian Root, Melatonin
Allergien: Sulfa Meds
Vorherige Impfungen: -

VAERS 2460557

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MI
Alter: 53,0
Geschlecht: F
Eingang: 26.09.2022
Impfdatum: 12.11.2021
Beginn: 18.09.2022
Tage bis Beginn: 310,0
Dosis: 2
Route/Site: - / -

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

Abdominal abscess Asthenia COVID-19 Clostridium test Debridement Decreased appetite Diarrhoea Discomfort Dizziness Drain placement Duodenal operation Enterocutaneous fistula Hypotension Incisional drainage Nausea Nothing by mouth order Pain Pyrexia

Symptomtext

Discharge Provider: MD Primary Care Provider: PA-C Admission Date: 9/18/2022 Discharge Date: Sep 25, 2022 PRESENTING PROBLEM: Intra-abdominal abscess Enterocutaneous fistula COVID-19 HOSPITAL COURSE: 54-year-old female with multiple intra-abdominal surgeries most recently an open enterocutaneous fistula takedown, repair of enterotomy, incision and drainage of right abdominal wall abscess and repair of duodenum on 7/21/2022 who is presenting with recurrence of her enterocutaneous fistula and intra-abdominal abscesses, now s/p wound exploration and debridement on 9/20/2022 with Dr. 9/18: Admitted, bedside I&D of right abdominal abscess 9/19: febrile overnight, ID consulted, IR planning drain today, NPO, +BM, 1L bolus for hypotension 9/20: No drainable collection per IR. Dressing changes. Consider TPN. Wound explored in the OR on 9/20/2022 with placement of malecot drain in the right abdominal wall abscess. Wound manager on the superior aspect of the midline. 9/21: Tolerating general diet. Malecot drain in right side - minimal output. Changed packing this morning near wound manager. 9/22: Tolerating general diet. Malecot drain in place with minimal output. Having BM and good UOP. Pain well controlled. 9/23: Dizziness/lightheadedness. Symptomatic. Nauseated. BM and voiding. Taking in PO intake. Still requiring IV dilaudid for dressing changes 9/24: Still endorsing weakness and heaviness with no appetite though 2200 mL oral intake recorded. Heart rate improved. Still up ambulating. Requiring IV Dilaudid for dressing changes. IV pain meds discontinued. Loose stools, C difficile pending 9/25: Pain significantly improved with dressing changes. Improved appetite without nausea or emesis. Up ambulating frequently. He feels comfortable doing dressing changes at home by herself. Ongoing loose stools, C difficile pending. Anticipate will initiate today really today and likely discharge home

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Praegender Schweregrund: Hypotension
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: History of ileostomy takedown, ileosigmoid anastomosis, lysis of adhesions >120 minutes 4/15/21 by Dr. History of ischemic colitis Postprocedural intraabdominal abscess complicated by enterocutaneous fistula History of DVT (deep vein thrombosis) Anemia Anxiety Asthma B12 deficiency Carpal tunnel syndrome Chronic pain Compression fracture of L5 vertebra Recurrent major depressive disorder, in partial remission Dyslipidemia Gastritis HTN (hypertension) IBS (irritable bowel syndrome) Insomnia S/P gastric bypass Seasonal allergies Vitamin D deficiency Autonomic neuropathy Right shoulder tendonitis Tenosynovitis, de Quervain Enterocutaneous fistula and intra-abdominal abscess s/p Ex-lap takedown of duodeno-cutaneous fistula with primary repair and serosal patch, repair of enterotomy x2 with drs. Pneumonia due to COVID-19 virus
Andere Medikamente: ALPRAZolam (XANAX) 0.5 MG tablet amoxicillin-clavulanate (AUGMENTIN) 875-125 MG per tablet ciprofloxacin (CIPRO) 500 MG tablet dicyclomine (BENTYL) 20 MG tablet DULoxetine (CYMBALTA) 30 MG delayed release capsule gabapentin (NEURONTIN) 300
Allergien: CyclobenzaprineHives, Rash FluoxetineHallucinations TramadolHives, Rash Seasonal
Vorherige Impfungen: -

VAERS 2408452

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge #033F21A

moderat

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 11.08.2022
Impfdatum: 16.04.2022
Beginn: 05.06.2022
Tage bis Beginn: 50,0
Dosis: 1
Route/Site: IM / LA

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

Body temperature increased COVID-19 Chest X-ray abnormal Pneumonia SARS-CoV-2 test positive

Symptomtext

06/05/2022- At home PCR test was positive for COVID-19. I notified my physician and she suggested I begin Vitamin C 3000 mg by mouth every day, D3, 10, 000 IU by mouth every day and Zinc 50 mg by mouth every day. 06/24/2022- Urgent care visit with temperature 103, pulse 120, pulse ox 93% and chest x-ray showing bilateral lower lobe pneumonia. Began Azithromycin 250 mg 6 tabs by mouth, Prednisone 50 mg by mouth every day x 5 days, Albuterol Sulfate 90 mcg 2 puffs every 6 hours as needed.

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Praegender Schweregrund: Pneumonia
Hospital-Tage: -
Labordaten: )6/05/2022- Use PCR Test for COVID-19 06/24/2022- Chest X-ray 2 views showing bilateral lower lobe pneumonia. 08/08/2022- Chest X-ray 2 views showing clear lower lobes.
Aktuelle Erkrankungen: none
Vorgeschichte: osteoarthritis bilateral knees, elevated cholesterol, hiatal hernia
Andere Medikamente: none
Allergien: sulfa, sulfites (includes wine, shrimp, etc), latex, nickel
Vorherige Impfungen: -

VAERS 2401298

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: IL
Alter: 78,0
Geschlecht: F
Eingang: 04.08.2022
Impfdatum: 09.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / -

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

Dyspnoea exertional Fatigue

Symptomtext

dyspnea on exertion, fatigue

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Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: HTN (Hypertension) Hypothyroidism Papillary carcinoma of thyroid (HCC) Type 2 diabetes mellitus without complication (HCC) Diabetic peripheral neuropathy (HCC) OSA (obstructive sleep apnea) - does not use CPAP Closed fracture of distal end of right ulna with routine healing Leg cramps Osteopenia with high risk of fracture Malignant neoplasm of cervix, unspecified site (HCC) Endometrial cancer (HCC) BMI 38.0-38.9,adult Medicare annual wellness visit, subsequent Other Breast CA (HCC) Trigeminal neuralgia-resolved with surgical intervention Other specified peripheral vascular diseases (HCC)
Andere Medikamente: ? Acetaminophen (TYLENOL ARTHRITIS PAIN PO) Take by mouth. ? acetaminophen-codeine (TYLENOL #3) 300-30 MG Tablet TAKE 2 TABLETS BY MOUTH NIGHTLY AS NEEDED FOR MODERATE OR MORE SEVERE PAIN. 180 Tablet 0 ? Alcohol Swabs (B-D SINGLE USE S
Allergien: - blue dyes -tegretol - xencial - paper tape - atorvastatin - lovastatin - fentanyl
Vorherige Impfungen: -

VAERS 2396438

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MI
Alter: 61,0
Geschlecht: M
Eingang: 29.07.2022
Impfdatum: 07.12.2021
Beginn: 19.02.2022
Tage bis Beginn: 74,0
Dosis: 3
Route/Site: - / -

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

Asymptomatic COVID-19 Hemiparesis Ischaemic cerebral infarction Magnetic resonance imaging head abnormal Paraesthesia SARS-CoV-2 test positive

Symptomtext

The patient was admitted on 2/19/2022 because of complaints of right-sided weakness. Patient was normal when he went to bed but woke up with weakness and paresthesias. No speech changes. Patient had PFO closure in 2020 after his previous CVAs.Patient was admitted, MRI and 2D echo were ordered. N MRI showed small area of acute/subacute ischemic infarct in the internal capsule area. Patient was continued on aspirin, Plavix and statin. During his hospital stay, patient became incidentally positive for COVID-19. He was asymptomatic. Arrangements were made for patient to go to inpatient rehab at local facility. Patient is currently on insulin sliding scale, his metformin and Trulicity are on hold here, can be resumed at local facility as per rehab physician's discretion.

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Praegender Schweregrund: Paraesthesia
Hospital-Tage: 2,0
Labordaten: Positive COVID-19
Aktuelle Erkrankungen: -
Vorgeschichte: Date Unknown Cancer of descending colon (HCC) Date Unknown Carotid atherosclerosis, bilateral Date Unknown CVA (cerebral vascular accident) (HCC) Date Unknown Heart disease Date Unknown HTN (hypertension) Date Unknown Hyperlipidemia Date Unknown Non-insulin dependent type 2 diabetes mellitus (HCC) Date Unknown PFO (patent foramen ovale)
Andere Medikamente: acetaminophen (TYLENOL) 325 MG tablet aspirin (HALFPRIN) 81 MG tablet atorvastatin (LIPITOR) 80 MG tablet Blood Glucose Monitoring Suppl (BLOOD GLUCOSE MONITOR KIT GENERIC) kit clopidogrel (PLAVIX) 75 MG tablet docusate sodium (COLACE)
Allergien: No known
Vorherige Impfungen: -

VAERS 2325434

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MI
Alter: 73,0
Geschlecht: M
Eingang: 21.06.2022
Impfdatum: 22.11.2021
Beginn: 11.06.2022
Tage bis Beginn: 201,0
Dosis: 3
Route/Site: - / -

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

Abdominal pain upper Alanine aminotransferase Aspartate aminotransferase Bile duct stone Biliary colic Biliary dilatation Blood alkaline phosphatase Blood bilirubin increased COVID-19 Chest X-ray abnormal Cholelithiasis Computerised tomogram abdomen abnormal Condition aggravated Cough Gallbladder disorder Gallbladder enlargement Hepatic cyst Hepatic enzyme increased

Symptomtext

Discharge Provider: MD Primary Care Provider: MD Admission Date: 6/11/2022 Discharge Date: 6/13/2022 PRESENTING PROBLEM: Choledocholithiasis [K80.50] COVID-19 virus infection [U07.1] HOSPITAL COURSE: Patient is a 73-year-old male with no significant past medical history who presented with right upper quadrant pain. He has noted intermittent right upper quadrant pain spontaneously resolved and had been ongoing for over a year. He has now been having more frequent and intense right upper quadrant pain. Patient was also experiencing fevers and a mild cough. In the emergency department he was found to be COVID positive and also found to have elevated liver enzymes. Chest x-ray showed hyperinflation but no infiltrates, edema or significant effusion Right upper quadrant ultrasound showed cholelithiasis with mild gallbladder wall thickening along with mildly dilated CBD. General surgery was contacted by the emergency department and they recommended admission for biliary colic and possible choledocholithiasis. CT abdomen pelvis was done and showed 2 simple benign hepatic cyst along with distension of the gallbladder, few calcified stones and thickening of the wall. Patient did not have any further abdominal pain after admission. General surgery felt that patient could have choledocholithiasis with passing of stones as his LFTs were improving and he was not having any further abdominal pain. Gastroenterology was consulted and they felt that there was low suspicion of CBD stone and did not feel there was any role for ERCP at this time. Gastroenterology stated that patient should follow-up with General surgery for cholecystectomy and IOC. Patient was started on a diet and tolerated this well without any increasing abdominal pain. Bilirubin was 3.3 on admission and had improved to 1.3. Alk-phos, AST and ALT all had decreased since admission. As LFTs were trending down and patient had no further abdominal pain-general surgery felt that he could discharge home and follow-up with them as an outpatient in 2 weeks time to discuss cholecystectomy. Patient had no other acute issues and was discharged home in stable condition 6/13/2022

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Praegender Schweregrund: Condition aggravated
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Biliary colic Calculus of gallbladder
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2318897

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: NY
Alter: 81,0
Geschlecht: F
Eingang: 14.06.2022
Impfdatum: 24.11.2021
Beginn: 19.12.2021
Tage bis Beginn: 25,0
Dosis: 3
Route/Site: IM / LA

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

Anticoagulant therapy Asthenia C-reactive protein increased COVID-19 COVID-19 pneumonia Cough Fatigue Fibrin D dimer Hypoxia Pyrexia SARS-CoV-2 test positive White blood cell count increased

Symptomtext

12/19/2021 - Came to ED with Fever, cough, fatigue for 3-4 days. BP 157/78, HR 97, RR 20, temp 96.8, SpO2-95% RA. Covid positive in ED. WBC 13.1, CRP 12.3. Admit Covid pneumonia. Doxycycline and Ceftriaxone initiated in ER. Not candidate for steroids/baricitinib/remedsivir o2 sat above 95%. 12/20 - Overnight became hypoxic 87%. Started on 2L O2NC. Improved to 95%. Started Baricitinib and Remdisivir. Temp elevated 99.9. All other vitals WNL. D-dimer 242. Continuing with Heparin. 12/21 - Weaning O2-97% on 2L via NC. Cough continues, weakness, however able to ambulate to bathroom. Temp 97.9 12/23 - Now on room air saturating 97%. IV antibiotics stopped after developing diarrhea. Diarrhea improved. Additional information for Item 18: 12/24 - Completed covid treatment course, weaned off O2 and doing well. Discharged to home.

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Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Multiple myeloma, HTN, CKD
Andere Medikamente: -
Allergien: Adhesive
Vorherige Impfungen: -

VAERS 2287521

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: VA
Alter: 50,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 18.11.2021
Beginn: 01.05.2022
Tage bis Beginn: 164,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Cough Dyspnoea Fatigue Oropharyngeal pain Paranasal sinus discomfort Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

April 30, 2022 I felt like I was a little congested like I had the start of a sinus infection. I woke up on April 31, 2022 with more sinus pressure thought I had the start of a sinus infection. I woke up around 1am on May 1, 2022 with low grade fever around 99.0 and a sore throat. Fever continued throughout the day so I decided to take a home test and it was positive. Fever did run 99.0-100.0 on and off, sinus pressure was still there, get winded very easily and the sore throat was worse. Called my doctor on Tuesday and she prescribed Paxlovid. Wednesday I started medication and noticed a little difference within 6 hours. Symptoms did gradually get better. Now I do feel very fatigued and have a dry cough.

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Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Rapid COVID-19 Home Test 05/01/2022 Positive
Aktuelle Erkrankungen: None
Vorgeschichte: High Blood Pressure
Andere Medikamente: Losartan 100mg daily Amlodipine 10mg daily
Allergien: Anti Inflammatory Product
Vorherige Impfungen: -

VAERS 2286944

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MI
Alter: 88,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 19.11.2021
Beginn: 17.05.2022
Tage bis Beginn: 179,0
Dosis: 1
Route/Site: IM / AR

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

Blister Blood sodium decreased COVID-19 Cough Dehydration Hyponatraemia Hypoxia Leukopenia Metabolic function test Mucosal disorder Nausea Pneumonia SARS-CoV-2 test positive

Symptomtext

Hospitalized (05/17/2022-05/19/2022); COVID-19 positive (05/17/2022); fully vaccinated plus booster HOSPITAL COURSE: this is a very pleasant 88-year-old lady with past medical history as listed who presents to the ER from her nursing facility with concerns of hypoxia. Patient states that she does not know why they brought her to the emergency department. Patient states that she has tested positive for bad yesterday. Patient is vaccinated and blistered. Patient denies any fever chills sweats. Patient has some nausea but denies any vomiting diarrhea. Patient does have a dry cough. Patient denies any chest pain or shortness of breath. Patient was confirmed to have COVID-19. Her sodium level was low and she was started on IV fluid hydration for dehydration. On her right wrist assessment patient had very dry mucous membranes. Per nursing and EMS patient was not hypoxic however they are having a hard time getting a good plaque. Patient did well during her hospital course. She did not require supplemental oxygen. She was hydrated and was anxious to go back to her facility. Patient will need repeat basic metabolic profile to monitor her sodium and renal function as well as a complete metabolic profile to monitor her white count. 1. Hyponatremia Secondary to dehydration. Patient was adequately hydrated. Repeat BMP at facility 2. COVID-19 Patient is vaccinated and boosted. Will hold off on dexamethasone as it is not clear if patient was actually hypoxic and there could be an interaction with her medications. Patient has not required supplemental oxygen. 3. Hypoxic Uncertain if event occurred. Patient has not been hypoxic for EMS nursing or required supplemental oxygen. 4. Chronic kidney disease stage 3 Monitor renal function. Avoid nephrotoxins. Appears around baseline 5. Leukopenia Likely secondary to her meds related to multiple myeloma as well as her underlying infection. Patient showed follow-up with her oncologist and have a complete blood count drawn at the facility to determine further workup 6. Pneumonia There was a question if patient had underlying bacterial pneumonia. Patient will be discharged with Ceftin for 5 days.

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Praegender Schweregrund: Dehydration
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension Unspecified essential hypertension Longstanding persistent atrial fibrillation (HCC) Heart failure with preserved ejection fraction (HCC) Chronic diastolic congestive heart failure (HCC) Cardiac pacemaker in situ Sinus node dysfunction (HCC) Pulmonary HTN (HCC) COVID-19 Multiple myeloma (HCC) Anemia PMR (polymyalgia rheumatica) (HCC) Knee pain, right Chronic kidney disease (CKD), stage III (moderate) (HCC) Prediabetes Hyponatremia Edema of both legs History of pulmonary embolus (PE) Animal bite of lower leg, right, sequela Hx of amiodarone therapy Long term current use of antiarrhythmic drug
Andere Medikamente: acetaminophen (MAPAP) 325 MG tablet ALPRAZolam (XANAX) 0.25 MG tablet ALPRAZolam (XANAX) 0.25 MG tablet amiodarone (PACERONE) 200 MG tablet apixaban (ELIQUIS) 2.5 MG tablet benzonatate (TESSALON) 200 MG capsule Brimonidine Tartrate (LUMIFY)
Allergien: NKA
Vorherige Impfungen: -

VAERS 2286944

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MI
Alter: 88,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 19.11.2021
Beginn: 17.05.2022
Tage bis Beginn: 179,0
Dosis: 3
Route/Site: IM / AR

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

Blister Blood sodium decreased COVID-19 Cough Dehydration Hyponatraemia Hypoxia Leukopenia Metabolic function test Mucosal disorder Nausea Pneumonia SARS-CoV-2 test positive

Symptomtext

Hospitalized (05/17/2022-05/19/2022); COVID-19 positive (05/17/2022); fully vaccinated plus booster HOSPITAL COURSE: this is a very pleasant 88-year-old lady with past medical history as listed who presents to the ER from her nursing facility with concerns of hypoxia. Patient states that she does not know why they brought her to the emergency department. Patient states that she has tested positive for bad yesterday. Patient is vaccinated and blistered. Patient denies any fever chills sweats. Patient has some nausea but denies any vomiting diarrhea. Patient does have a dry cough. Patient denies any chest pain or shortness of breath. Patient was confirmed to have COVID-19. Her sodium level was low and she was started on IV fluid hydration for dehydration. On her right wrist assessment patient had very dry mucous membranes. Per nursing and EMS patient was not hypoxic however they are having a hard time getting a good plaque. Patient did well during her hospital course. She did not require supplemental oxygen. She was hydrated and was anxious to go back to her facility. Patient will need repeat basic metabolic profile to monitor her sodium and renal function as well as a complete metabolic profile to monitor her white count. 1. Hyponatremia Secondary to dehydration. Patient was adequately hydrated. Repeat BMP at facility 2. COVID-19 Patient is vaccinated and boosted. Will hold off on dexamethasone as it is not clear if patient was actually hypoxic and there could be an interaction with her medications. Patient has not required supplemental oxygen. 3. Hypoxic Uncertain if event occurred. Patient has not been hypoxic for EMS nursing or required supplemental oxygen. 4. Chronic kidney disease stage 3 Monitor renal function. Avoid nephrotoxins. Appears around baseline 5. Leukopenia Likely secondary to her meds related to multiple myeloma as well as her underlying infection. Patient showed follow-up with her oncologist and have a complete blood count drawn at the facility to determine further workup 6. Pneumonia There was a question if patient had underlying bacterial pneumonia. Patient will be discharged with Ceftin for 5 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension Unspecified essential hypertension Longstanding persistent atrial fibrillation (HCC) Heart failure with preserved ejection fraction (HCC) Chronic diastolic congestive heart failure (HCC) Cardiac pacemaker in situ Sinus node dysfunction (HCC) Pulmonary HTN (HCC) COVID-19 Multiple myeloma (HCC) Anemia PMR (polymyalgia rheumatica) (HCC) Knee pain, right Chronic kidney disease (CKD), stage III (moderate) (HCC) Prediabetes Hyponatremia Edema of both legs History of pulmonary embolus (PE) Animal bite of lower leg, right, sequela Hx of amiodarone therapy Long term current use of antiarrhythmic drug
Andere Medikamente: acetaminophen (MAPAP) 325 MG tablet ALPRAZolam (XANAX) 0.25 MG tablet ALPRAZolam (XANAX) 0.25 MG tablet amiodarone (PACERONE) 200 MG tablet apixaban (ELIQUIS) 2.5 MG tablet benzonatate (TESSALON) 200 MG capsule Brimonidine Tartrate (LUMIFY)
Allergien: NKA
Vorherige Impfungen: -

VAERS 2267426

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MD
Alter: 58,0
Geschlecht: M
Eingang: 09.05.2022
Impfdatum: 11.05.2021
Beginn: 25.09.2021
Tage bis Beginn: 137,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Blood test normal Cardiac stress test normal Chest discomfort Condition aggravated Dyspnoea Electrocardiogram abnormal Heart rate increased Thyroid function test normal Tinnitus Ultrasound scan normal

Symptomtext

Atrial Fibrillation (AFib) - Shortness of breath; tightness in chest; high heart rate. ECGs showing AFib I go into AFib several times per week lasting several hours to several days. I have not history of heart issues prior to receiving the COVID vaccine. ALSO: I had a low level of Tinnitus prior to first vaccine shot. Three days after the first shot, the volume of the ringing in my ears more than double and still exists today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: EKG - Normal at the time Stress Test - Passed with flying colors Sonogram of heart - Nothing out of the ordinary Blood work - Nothing out of the ordinary Thyroid Test - Negative
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Multivitamin, Omega oil, Vitamins A,C,D,E, Iron, Zinc, Doxy
Allergien: none
Vorherige Impfungen: -

VAERS 2261771

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: DE
Alter: 75,0
Geschlecht: F
Eingang: 03.05.2022
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Arthropathy Bronchitis Computerised tomogram normal Dyspnoea Fatigue Illness Impaired self-care Influenza Magnetic resonance imaging abnormal Muscular weakness Nasopharyngitis Neck pain Oropharyngeal pain Pain Pain in extremity Pyrexia SARS-CoV-2 test negative Sleep disorder

Symptomtext

11/09/2021 Around noon I started experiencing flu symptoms. I was fatigued, had a low-grade fever and hurt all over. This lasted 24 hours. The next time I was sick was Dec. 1, 2021. I was sick for over 14 days with a horrific sore throat. Then I got the worse head type cold, I was up all-night coughing and had trouble breathing. I tested negative for COVID-19. I went to the ER. They did x-rays and a CT. I was diagnosed with bronchitis, and they gave me an antibiotic and cough syrup. It started to get better the middle of December. It was at that time, my upper arm started to hurt me really bad. I thought it was because I was in bed so much and coughing so much. As time went on, my arms became worse to the point where I could not sleep at night. I can't put my eye drops in or get dressed by myself. I am having a hard time. I continue to have problems with my arms. On March 23,2022, I had an appointment with neurologist APN. I started thinking it was not fibromyalgia. I was having neck pain and upper arms still hurt. She examined and said there was a weakness in my arms. She ordered an MRI. An MRI was done on 4/15/2022. It showed interval development of modern edema in the Left C3-C4, and Right C4-C5 articulating facet and development of periarticular inflammatory stranding in the adjacent fat plains suggesting active arthropathy. Involvement of the left C4 and right C4 is suspected. There is a stable reduction at C5 and C6. There is a 5m collection of fluid in the sub tissue overly left C3. There is clinical concern for septic arthritis or possibility of a small periarticular access. Finding could be synovial cyst. There is a mild core compression and C4,C5 and C5, C6. Physiotherapy was ordered and I started it on 4/25/2022. Tomorrow, I will see a neurosurgeon. The physiotherapist, said she is very interested in what the effects of COVID-19 vaccines have on people with Fibromyalgia.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: I tested negative for COVID-19. X-rays and a CT revealed bronchitis, MRI - interval development of modern edema in the Left C3-C4, and Right C4-C5 articulating facet and development of periarticular inflammatory stranding in the adjacent fat plains suggesting active arthropathy. Involvement of the left C4 and right C4 is suspected. There is a stable reduction at C5 and C6. There is a 5m collection of fluid in the sub tissued overly left C3. There is clinical concern for septic arthritis or possibility of a small periarticular access. Finding could be synovial cyst. There is a mild core compression and C4,C5 and C5, C6.
Aktuelle Erkrankungen: None
Vorgeschichte: Fibromyalgia, Sleep Apnea, Hypothyroidism, High Blood Pressure, Arthritis, Meniere's Disease, Bradycardia, Whipple Pancreatic surgery, Liver issues
Andere Medikamente: Synthroid .112 mg, Norvasc 5mg, Losartan HCZ 100-12.5, PROair, Juice Plus, Multi Vitamin, Calcium Citrate, Zinc, Probiotic, Barley Brass
Allergien: Clindamycin
Vorherige Impfungen: -

VAERS 2238865

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: GA
Alter: 28,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Chest discomfort Echocardiogram Electrocardiogram ambulatory abnormal Electrocardiogram normal Feeling abnormal Heart rate increased Palpitations Sinus tachycardia

Symptomtext

I went to bed early because I was starting to feel some minor side effects of my vaccine. Around 10pm (12 hours after my booster shot), my Watch woke me up because a high heart rate had been detected for 20 minutes. My heart rate is typically in the 60's, but this time it was 168. It stayed there for about 4 hours before eventually falling down to around 100. I went to the doctor 2 days later, on Monday 11/8 and had an EKG done. It was normal, but the doctor recommended a 48 hour holter monitor test to be sure, but I could not get the monitor until after my second episode, which was about a week after my first (this time, my heart rate climbed into the 150's). The holter monitor showed inappropriate sinus tachychardia. A month later, I had another episode, but not quite as high (around 130). And a month after that, I had one last episode around 120. All in all, I felt "off" for about a month total - my heart rate was higher than usual and my chest felt full. Each "big" episode was in the middle of the night, when I was asleep and awoke to my heart racing for no reason.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: EKG 11/8/21 Holter Monitor began 11/15/21 Echo 12/2/21
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism, cold-induced asthma, hemochromatosis gene carrier, interstitial cystitis, eczema
Andere Medikamente: Synthroid, B12 supplement
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2228732

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: GA
Alter: 59,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 17.11.2021
Beginn: 02.01.2022
Tage bis Beginn: 46,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Chest discomfort Chest pain Chills Cough Dyspnoea Fatigue Headache Oropharyngeal pain Pain Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

I contracted COVID-19 1/2/22 with symptoms of fever 100, chills, fatigue, cough, body aches, shortness of breathe, chest tightness/pain, headache, sore throat, congestion. I was prescribed a Z-pack and antibiotics. It took me 4 weeks to fully recover.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Rapid nasal swab was positive for COVID-19 1/6/22
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Estradiol, HCTZ for blood pressure, Lisinopril, Venlafaxine, Pantoprazole, Torbastatine
Allergien: None
Vorherige Impfungen: -

VAERS 2228432

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: GA
Alter: 40,0
Geschlecht: F
Eingang: 12.04.2022
Impfdatum: 12.12.2021
Beginn: 29.12.2021
Tage bis Beginn: 17,0
Dosis: 3
Route/Site: IM / RA

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

Asthma Condition aggravated Pulmonary function test Steroid therapy

Symptomtext

About a week and a half after vaccine I developed asthmatic symptoms unlike symptoms I have had before. I hadn't used any of my asthma medications since December 2019. Went to see the asthma specialist and got medications on Jan 4th. Received steroid shots and prescribed steroid pack and nebulizer. Symptoms began improving and cleared completely in about 2 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Lung function test.
Aktuelle Erkrankungen: No
Vorgeschichte: Asthma
Andere Medikamente: Multivitamin; Vitamin C; Vitamin D
Allergien: Aspirin; NSAIDS; Peanuts
Vorherige Impfungen: -

VAERS 2206653

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MA
Alter: 51,0
Geschlecht: F
Eingang: 30.03.2022
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Arthritis Asthenia Condition aggravated Inflammation Joint impingement Joint range of motion decreased Myalgia Nervousness Pain Pain in extremity Rotator cuff syndrome Tendonitis X-ray abnormal

Symptomtext

I usually experience a sore arm for a week or so after a flu or COVID vaccine. With this one (the COVID booster), the soreness in my upper arm did not fade after a week or so but instead got worse and spread across my shoulder and up into my trapezius muscles. .After about a month, I consulted my doctor and started physical therapy. Xrays showed mild early arthritis in my left shoulder, but when I was examined by a physical therapist on December 8, she observed impingement and tendinitis in my left arm and shoulder area, with inflammation particularly acute in the tendons that connect my bicep and supraspinatus muscles to my shoulder. While my range of motion and strength have both improved following a course of physical therapy, I still experience pain multiple times a day during the course of routine activities (washing dishes, getting dressed, getting into the car, any weight bearing exercise, etc.) I think that either the COVID booster injection was administered too high in my arm and triggered SIRVA, or my body had an excessive inflammatory response to the booster that triggered tendinitis and perhaps frozen shoulder that will take more time to resolve. I'm now five months out from my booster shot and want to get a fourth shot given my auto-immune disease profile, but I'm nervous about this happening again. I would welcome advice on this subject.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: 11/30/21 examination in doctor's office 12/1/21 (approximate date) x-ray at Medical Center 12/8/21 physical therapy examination (Medical Center) January-February, 2022 weekly physical therapy sessions, with self-guided physical therapy exercises since then.
Aktuelle Erkrankungen: -
Vorgeschichte: Celiac disease, Hashimoto's hypothyroiditis, mild asthma
Andere Medikamente: Levothyroxine 88 mcg daily, multivitamin
Allergien: Gluten, avelox
Vorherige Impfungen: -

VAERS 2196935

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

moderat

Staat: IL
Alter: 57,0
Geschlecht: F
Eingang: 24.03.2022
Impfdatum: 12.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Anxiety Blister Magnetic resonance imaging Rash Rheumatoid factor Tremor

Symptomtext

bliters, rash,shakes, anxiety

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: rheumatory factors, nuclear tests
Aktuelle Erkrankungen: -
Vorgeschichte: gilliam burres
Andere Medikamente: vit c, b, zinc
Allergien: -
Vorherige Impfungen: fluzone

VAERS 2192293

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: IL
Alter: 74,0
Geschlecht: F
Eingang: 22.03.2022
Impfdatum: 22.11.2021
Beginn: 14.02.2022
Tage bis Beginn: 84,0
Dosis: 3
Route/Site: IM / RA

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

Acute myeloid leukaemia Anaemia Aspiration Aspiration pleural cavity COVID-19 Cardiac failure congestive Cardiomegaly Chest X-ray abnormal Condition aggravated Dyspnoea Endotracheal intubation Haemoglobin abnormal Hypoxia Lung disorder Myelodysplastic syndrome Oedema Pancytopenia Pleural effusion

Symptomtext

Patient received moderna vaccine on 3/8/21, 4/5/21 and 11/22/21. COVID positive on 2/14/22. Patient admitted at an outside hospital on 2/14/22. She worsened with hypoxia and intubated. Transferred to this hospital on 3/6/22. Was on antibiotics that were broad-spectrum and underwent pancultures. Was also found early in the hospitalization have a left-sided pleural effusion and underwent thoracentesis with significant improvement of continued dyspnea. Had an acute anemia on chronic and also pancytopenia. Required transfusion and after transfusion of packed red blood cells hemoglobin remained stable. Was started on Neupogen as well. She has MDS and AML as noted above. Chemotherapy was on hold until current issues were resolved. Hematology followed in the hospital. Was continued on home blood pressure medications and blood pressure and heart rate remained stable throughout her hospitalization. Oxygen titrated for best affect. Was found positive in her inflammatory exudate for S per kilos this. Was started on voriconazole at loading dose and then to have a course of 12 weeks of treatment. Was continued on vancomycin and Zosyn to completion. Doxycycline was 100 mg b.i.d. as well for 7 days and then back to suppressive dose per Oncology. Continued with generalized improvement in terms of her exercise capacity. Physical therapy and occupational therapy followed and cleared patient to return home with family help. Discharged on 3/17/22

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: 11,0
Labordaten: 2/14/22 COVID19: positive 2/18/22 chest xray: Mild cardiomegaly with bilateral airspace disease left greater than right and bilateral pleural effusions. Findings likely related to edema and CHF. Superimposed pneumonia specially within the left lung however is questioned. 3/14/22 chest xray: Improving pneumonia or aspiration.
Aktuelle Erkrankungen: -
Vorgeschichte: thoracic aortic aneurysm , colon cancer with mets to the ovary and lung, MDS, PVD, CAD, COPD
Andere Medikamente: acyclovir 200 MG Caps Commonly known as: ZOVIRAX 400 mg, Oral, 3 TIMES DAILY albuterol 0.63 MG/3ML Nebu Commonly known as: ACCUNEB 3 mL, Nebulization, EVERY 6 HOURS PRN allopurinol 300 MG Tabs Commonly known as: ZYLOPRIM 300 mg, Oral, D
Allergien: macrobid
Vorherige Impfungen: -

VAERS 2188002

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: VA
Alter: 60,0
Geschlecht: F
Eingang: 18.03.2022
Impfdatum: 28.09.2021
Beginn: 23.02.2022
Tage bis Beginn: 148,0
Dosis: 3
Route/Site: SYR / LA

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

Bronchitis COVID-19 Cough Dyspnoea Headache Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive

Symptomtext

I had headache, body aches, sore throat, fever, cough, and difficulty breathing. These symptoms lasted for about 2 weeks but the cough and breathing issue turned into to COVID-19 bronchitis. On Feb 23rd and March 2nd, I tested positive for COVID-19 for both test.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: COVID-19 test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Fibromyalgia
Andere Medikamente: N/A
Allergien: Zeropointone; Aspirin
Vorherige Impfungen: -

VAERS 2151123

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: VA
Alter: 62,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 07.12.2021
Beginn: 01.12.2021
Tage bis Beginn: -
Dosis: 2
Route/Site: SYR / RA

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

Blood test Cardiac flutter Echocardiogram Electromyogram Hypoaesthesia Paraesthesia Vitamin D deficiency

Symptomtext

I noticed a flutter in my heart. Then, I began to have numbness and tingling in my hands. These are still ongoing as of today. I went to the doctor about this. They referred my to a cardiologist for Echocardiogram. I was also referred to a neurologist for an EMG test, which is a nerve test, shows little to no nerve conduction. They did also did blood work, vitamin d deficiency.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Blood work Echocardiogram EMG test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Celiac, Thyroid disorder
Andere Medikamente: A beta blocker
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2122883

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: NJ
Alter: 63,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 12.12.2021
Beginn: 17.02.2022
Tage bis Beginn: 67,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest X-ray normal Chest discomfort Chest pain Cough Dyspnoea Electrocardiogram normal Exposure to SARS-CoV-2 Fatigue Fibrin D dimer normal Hyperhidrosis Laboratory test abnormal SARS-CoV-2 antibody test SARS-CoV-2 test positive Troponin normal

Symptomtext

63 year old male with hx HTN, Pre diabetes, HLD, BPH, presents for evaluation of SOB and midsternal chest discomfort-pressure like pain which occured when he went to the bathroom. He had a cough and fatgue over last weekend and tested positive for COVID 19 on 2/15/22. His wife and child are ill with COVID as well, mild symptoms. He is fully vaccincated and was boosted on 12/12/21 with pfiezer. In the ED he had a chest xray which was negative, he is not hypoxic, 100% on room air, no acute ecg changes, and d dimer is negative, otherwise his markers are minimaly elevated. He has no fever or chills but broke into a sweat. No nausea or vomiting or changes in taste or smell. Troponin negative so far and he had a baby aspriin in the ED.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: 2,0
Labordaten: 02/17/2022 - SARS-CoV-=2 Antigen (++); IgM 0.31, IgG 0.03; IgG2 QT-SPIKE >25,000
Aktuelle Erkrankungen: -
Vorgeschichte: severe anaphlyaxis to augmentin and tessalon pearles 2017 HTN HLD BPH GERD pre diabetes. Significant Surg Hx As Listed Addt'l Surgical History vasectomy. Smoking Status Never Smoker.
Andere Medikamente: "ACTIVE - HYDROCHLOROTHIAZIDE 25MG BY MOUTH DAILY" "ACTIVE - PROTONIX 40MG BY MOUTH DAILY" atorvastatin 20 mg Tablet Extended Instructions: (ATORVASTATIN (20 MG TABLET) 1 tablet by mouth daily) ACTIVE - ATORVASTATIN (20 MG TABLET) 1 tablet
Allergien: Augmentin and Tessalon Perles
Vorherige Impfungen: -

VAERS 2113140

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MD
Alter: 30,0
Geschlecht: F
Eingang: 15.02.2022
Impfdatum: 10.11.2021
Beginn: 05.02.2022
Tage bis Beginn: 87,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Iritis

Symptomtext

I had an iritis flare up that started on 02/05/2022. On 02/07/2022 I went to the doctor and they just looked in my eye and diagnosed it. They gave me Prednisolone Acetate eye drops. It is still ongoing and it is going to take a couple of weeks to go away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Autoimmune disease- iritis anterior uveitis (acute one)
Andere Medikamente: Fluoxetine HCL, Metoprolol SUCC, Mylan birth control
Allergien: Seasonal
Vorherige Impfungen: -

VAERS 2110294

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: OH
Alter: 72,0
Geschlecht: M
Eingang: 14.02.2022
Impfdatum: 18.11.2021
Beginn: 09.02.2022
Tage bis Beginn: 83,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cardiac stress test normal Cardiac telemetry normal Chest X-ray normal Dyspnoea Dyspnoea exertional Echocardiogram normal Ejection fraction normal Limb injury Myocardial necrosis marker normal SARS-CoV-2 test positive

Symptomtext

The patient is a 72 y.o. male who presented with dyspnea on exertion. Pt c/o severe breathlessness with minimal exertion that started 2-3 days ago. He denies dyspnea at rest. Denies CP. No fevers or cough. Has history of CAD. Was found to be COVID positive. No hypoxia and no infiltrates on CXR. He is vaccinated. " Hospital Course: The patient was admitted to the hospital and was evaluated and treated per below. * Dyspnea on exertion o Dyspnea on exertion with concern about possible angina equivalent. He is Covid positive and fully vaccinated. No IV Remdesivir or steroids initiated on admission. Chest x-ray showed no focal consolidation. Patient reported feeling better following admission with progressive resolution of his shortness of breath. His serial cardiac enzymes remained negative ruling out acute coronary syndrome. Telemetry was uneventful. Echocardiogram was done showing normal ejection fraction. Myoview cardiac stress test was done showing normal study. With patient's symptoms gradually resolving and the absence of chest pain patient was discharged home to follow up on outpatient basis. o Diabetes mellitus type 2. Continue with same home regimen/equivalent. Monitor blood sugar and cover with insulin sliding scale. o Hypertension. Controlled. Continue same treatment. Follow up daily labs. o Foot wound. Followed outpatient. Currently on doxycycline. Continue course as prescribed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: PAD, Aortic Stenosis, HTN, Gout, HLD, Type 2 Diabetes,
Andere Medikamente: ASA, Iron, urocit-K, spiralactone, altace, tricor, zyloprim, flomax, lasix, lozol, zocor, lopressor, tresiba, victoza, monodoxycyline,
Allergien: Bees
Vorherige Impfungen: -

VAERS 2101953

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: AZ
Alter: 77,0
Geschlecht: M
Eingang: 10.02.2022
Impfdatum: 15.11.2021
Beginn: 03.02.2022
Tage bis Beginn: 80,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Dyspnoea Interchange of vaccine products Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

78 year old male with pmedhx significant for prediabetes, CKD, arthritis of knee, HTN. Pt presented to the ER 2/3/2022 with shortness of breath, congestion, and cough x 1 week. He has hx of Pfizer COVID vaccination x 2 with a Moderna booster over two monts ago. SpO2 in ER is 92% on 2L NC. Abbott COVID+ in ER. Pt admitted to specialized CU for further care. Required 1L of O2 transiently at rest but up to 3L with ambulation following admission. He received dexamethasone and remdsivir during his stay. At the time of d/c on 2/6/2022, he was able to maintain O2 saturation in the 90%s at rest and with ambulation. Stable for d/c home with close O2 monitoring.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: 3,0
Labordaten: Abbott COVID+ on 2/3/2022.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: CKD, Arthritis, Prediabetes, HTN
Andere Medikamente: unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 2098269

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: PA
Alter: 61,0
Geschlecht: F
Eingang: 09.02.2022
Impfdatum: 10.11.2021
Beginn: 15.01.2022
Tage bis Beginn: 66,0
Dosis: UNK
Route/Site: SYR / -

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

Lip exfoliation Lip pain Lip swelling Pain Paraesthesia oral Tenderness

Symptomtext

Fat lips, sore lips, constant peeling of lips, tingly lips, very sensitive and sore, cycling of issue - lips get really fat, peel, peel and peel some more, go down and the cycle starts all over again

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia oral
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: lichen schlerosis
Andere Medikamente: only vitamins- Ritual for Women over 50
Allergien: sulfa
Vorherige Impfungen: Covid19 Pfizer Vaccine, original 2 dose vaccine for me

VAERS 2076000

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: IL
Alter: 59,0
Geschlecht: F
Eingang: 31.01.2022
Impfdatum: 01.11.2021
Beginn: 27.12.2021
Tage bis Beginn: 56,0
Dosis: 3
Route/Site: SYR / RA

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

Adverse event Arthralgia Burning sensation Chest X-ray Chest discomfort Electrocardiogram normal Erythema Fatigue Feeling abnormal Full blood count Oesophagitis Oropharyngeal pain Paraesthesia Pruritus Skin tightness Throat tightness Urticaria Vision blurred

Symptomtext

Adverse events occurred after Christmas Day, 2021 and before New Year's Day, 2022: Woke up in morning with the following adverse reactions: sore throat, esophageal tightness, chest tightness, scalp and ears: tingling, burning, itching, red, swelling, hives followed by the same on my upper and lower torso, arms, hands, legs, thighs, feet and face. All symptoms intense - from a number standpoint, 10's across the line. I then noticed extreme fatigue, blurred vision and joint pain in my knees and fingers. On day two of these symptoms I went to Urgent Care and was prescribed 5 days of prednisone, Benadryl and topical anti itch cream (cortisone and calamine). I am still experiencing all of these symptoms as of today (1/31/2022). After 3 days of still experiencing the symptoms with no relief, I went to ER. My treatment consisted of intravenous water, Benadryl and steroid. Prescribed more steroids and Benadryl for home. Still, nothing. Symptoms remained. Decided to go again to ER because of no change and was given the same thing and told there was nothing else they could do - told to make an appointment with doctor and allergist. Made appointment with family doctor and was put on Dosapin a medication used for depression. Doctor told me that he was getting one or two people a week coming in with the same symptoms as was told that it could be from vaccine and that his some of his patients were having luck with this medicine. I was told to take for three months and then come back for follow up. The dosapin helped a bit but put my entire body on lock down, mentally and physically, I could not do anything except sleep and felt like I was not coherent at all. I immediately called the doctor and he said to go off it and take Benadryl and anti itch cream and prescribed me to also take Zytec. Nothing was relieving my symptoms still! I decided to go to an allergist, whom I found out, suffered the same symptoms! The doctor prescribed me what he took - Benadryl, Zyzal, Zyrtec, Pepcid and anti itch creme (cortisone and calamine). I also made an appointment, per his request, for allergy testing. I was told that I had to go off all histamines for 7 - 10 days prior to testing. I was on my second day of not taking the histamines and I felt like I just wanted to die! All of the above symptoms were multiplied by 2 - they were so intense and unbearable. I called the testing site and told them I would have to wait until I was cleared up due to the face that my symptoms were so unbearable without the antihistamine medications prescribed. As of today (1/31/2022), I am still having the same symptoms - they come and go and decide where they want to go on my body - there is no relief.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Medical tests at the Emergency Room - last week of December, 2021 and first week of January 2022: EKG for heart, chest X-ray, lower and upper gastrointestinal contrasting X-ray, complete cbc. Was told no heart problems (heart attack) due to esophageal tightness. Xray of esophagus indicated inflamed esophagus and to contact allergist and family doctor which was done (read item 18 above)
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Lexapro (Escitolopram), Atorvastatin, Melatonin, Advil, Aleve
Allergien: none
Vorherige Impfungen: -

VAERS 2051125

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

moderat

Staat: NC
Alter: 45,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 03.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: IM / LA

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

Hypoaesthesia Injection site hypoaesthesia Injection site paraesthesia Paraesthesia

Symptomtext

Two weeks after vaccination patient states he started having numbness and tingling in his left deltoid and both hands that has not resolved after two months.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site paraesthesia
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Asthma
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2050128

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: RI
Alter: 23,0
Geschlecht: M
Eingang: 20.01.2022
Impfdatum: 22.12.2021
Beginn: 02.01.2022
Tage bis Beginn: 11,0
Dosis: 1
Route/Site: OT / LA

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

Dyspnoea Erythema Inflammation Pruritus Pyrexia Urticaria Vaccination site pain

Symptomtext

having difficulty breathing, feels slight constriction in lungs; At this ti me sti ll experiencing hives across the body(though the severity has lessened significantly). feeling a slight constant pain in the area where received the shot, localized soreness In the area where received the shot; feel the skin in the itchy areas becoming inflamed/ears and neck were completely red and enflamed; began to experience itching on scalp and neck region; ears and neck were completely red and enflamed; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (began to experience itching on scalp and neck region), ERYTHEMA (ears and neck were completely red and enflamed), DYSPNOEA (having diffi cultybreathing, feels slight constriction in lungs), INFLAMMATION (feel the skin in the itchy areas becoming inflamed/ears and neck were completely red and enflamed) and URTICARIA (At this ti me sti ll experiencing hives across the body(though the severity has lessened signifi cantly).) in a 23-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 22-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .25 milliliter. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 02-Jan-2022, the patient experienced ERYTHEMA (ears and neck were completely red and enflamed). On 02-Jan-2022 at 10:00 PM, the patient experienced PRURITUS (began to experience itching on scalp and neck region) and INFLAMMATION (feel the skin in the itchy areas becoming inflamed/ears and neck were completely red and enflamed). On an unknown date, the patient experienced DYSPNOEA (having difficulty breathing, feels slight constriction in lungs), URTICARIA (At this ti me sti ll experiencing hives across the body(though the severity has lessened significantly).) and VACCINATION SITE PAIN (feeling a slight constant pain in the area where received the shot, localized soreness In the area where received the shot). At the time of the report, PRURITUS (began to experience itching on scalp and neck region), ERYTHEMA (ears and neck were completely red and enflamed), DYSPNOEA (having difficulty breathing, feels slight constriction in lungs), INFLAMMATION (feel the skin in the itchy areas becoming inflamed/ears and neck were completely red and enflamed) and VACCINATION SITE PAIN (feeling a slight constant pain in the area where received the shot, localized soreness In the area where received the shot) outcome was unknown and URTICARIA (At this ti me sti ll experiencing hives across the body(though the severity has lessened significantly.)had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature: 97.7 (abnormal) 97.7F. No concomitant medications were reported. Patient woke up next morning to an even worse reaction than patient was having before. Patient went to see a dermatologist and was prescribed several (unspecified) medications to treat hives. Dermatologist believed that patient may be experiencing a delayed allergic reaction to the proteins present in the booster. Patient have strong belief that my adverse reactions are related to my receiving of the Moderna booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Test Name: Body temperature; Result Unstructured Data: 97.7F.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2014915

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MA
Alter: 52,0
Geschlecht: F
Eingang: 07.01.2022
Impfdatum: 02.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / LA

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

Tremor

Symptomtext

Novocaine at dentist office for a routine procedure took 12 hours to wear off (usually takes 2-4 hours) 2 days after booster I have also had internal tremors that started a week or two after the shot and are finally subsiding. I have a very good friend who, like me, is very healthy, active and fit who also got internal tremors after her Moderna vaccine. She also has had unexplained muscle spasms and had had a full neurological workup with no significant findings All three of my boosters triggered a minor psoriasis inflammation (I do not typically have psoriasis) I am thrilled that I am vaccinated and would suffer through these adverse effects again if required. I am just reporting them because I believe the vaccines are triggering more symptoms in people than doctors might be associating with the shots

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: None. I did tell my dentist about the novocaine not wearing off until midnight for a 10am procedure and he thought it was unusual but did not seem particularly inclined to think it could be related to the Moderna booster
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2014567

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: VA
Alter: 46,0
Geschlecht: F
Eingang: 07.01.2022
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: ja

Asthma Condition aggravated Erythema Nausea Peripheral swelling Pruritus Urticaria

Symptomtext

Swollen, red, itchy arm for 5 days, asthma attack, nausea, hives

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: n/A
Aktuelle Erkrankungen: asthma and HBP
Vorgeschichte: asthma and HBP, allergies
Andere Medikamente: Zyrtec 10 MG, Montelukast 10MG, Breo Elipta 200/25, Vitamin D 2000 IU, amlodipine 5 MG, allergy shots.
Allergien: anaphylaxis to sulfur, penicillin and related antibiotics, anthramycin and related antibiotics, Cefalcor, ciproflaxon, seasonal allergies. Sept had anaphylaxis
Vorherige Impfungen: -

VAERS 2010517

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: GA
Alter: 67,0
Geschlecht: M
Eingang: 06.01.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Hypoaesthesia Paraesthesia

Symptomtext

NUMBNESS IN ARM, FINGERTIPS, STRANGE TINGLES IN DIFFERENT PARTS OF BODY AFTER INJECTION

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: EGGS
Vorherige Impfungen: ANY EGG BASED VACCINE

VAERS 2007059

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MA
Alter: 30,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 15.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 9,0
Dosis: UNK
Route/Site: SYR / LA

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

Arthralgia Dyspnoea Joint swelling Pharyngeal swelling Swelling face Urticaria

Symptomtext

Joint swelling, joint pain, hives, urticaria, throat swelling, trouble breathing and chest pain. Treatment: 3 rounds of steroids, Zyrtec daily and famotidine daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Birth control
Allergien: Sulfa drugs and Amoxicillin
Vorherige Impfungen: -

VAERS 1989279

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: OH
Alter: 23,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Back pain Chest pain Chills Pyrexia

Symptomtext

I woke up the night after getting the booster with normal and expected fever and chills. However, as the night went on, I started having sharp chest pains in the center of my chest. The following 3 or 4 days, I kept experiencing the pain in my chest as well as sharp pains in my back that would come and go.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None. I never went to see a physician or healthcare provider when I was experiencing symptoms.
Aktuelle Erkrankungen: Nonw
Vorgeschichte: None
Andere Medikamente: Sprintec
Allergien: None
Vorherige Impfungen: -

VAERS 1981592

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: TX
Alter: 50,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 06.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal distension Appetite disorder Brain natriuretic peptide increased Cardiac disorder Dyspnoea Ejection fraction decreased Heart rate increased

Symptomtext

Heart is not working right. Fast heartbeat, short of breath, bloating, co appetite. Checked in hospital. Still under treatment in hospital

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: BNP is 1000 around EF 25-30 %
Aktuelle Erkrankungen: Pre diabetic
Vorgeschichte: No
Andere Medikamente: Diabetic and cholesterol drugs
Allergien: No
Vorherige Impfungen: -

VAERS 1980568

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MA
Alter: 52,0
Geschlecht: F
Eingang: 25.12.2021
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Asthenia Body temperature Burning sensation Chills Discomfort Fatigue Gait disturbance Headache Illness Insomnia Interchange of vaccine products Malaise Mobility decreased Myalgia Pyrexia Vaccination complication Visual impairment

Symptomtext

no energy to be siting more than 30 minutes; entire body was burning for 30 hours; could not walk / difficult task to get to the bathroom; did not sleep in 30 hours; shivers; She had received a primary vaccine series of the Pfizer covid-19 vaccine and received a booster dose of the Moderna covid-19 vaccine; She lied in bed up through the entire day yesterday; fever; muscle pain /aches; headache; Her whole body loosened up, like you just came out of anesthesia or like her body was out of power,She was unable to get up and make any food for; felt a little mild, like you don't have to think a lot.; just a little uncomfortable; grade 4 side effects; She was unable to get up and make any food for herslef; She also could not see straight when pouring her kettle of water.; This spontaneous case was reported by a physician and describes the occurrence of MALAISE (felt a little mild, like you don't have to think a lot.), DISCOMFORT (just a little uncomfortable), VACCINATION COMPLICATION (grade 4 side effects), MOBILITY DECREASED (She was unable to get up and make any food for herslef) and VISUAL IMPAIRMENT (She also could not see straight when pouring her kettle of water.) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Small bowel obstruction and Bowel obstruction surgery (small bowel obstruction). Previously administered products included for COVID-19 vaccination: Pfizer covid-19 vaccine (Pfizer EW0171) on 30-Apr-2021 and Pfizer covid-19 vaccine (Pfizer EW0185 Experienced symptoms with the second dose of the vaccination series.) on 21-May-2021. Past adverse reactions to the above products included Adverse event with Pfizer covid-19 vaccine; and No adverse event with Pfizer covid-19 vaccine. Concurrent medical conditions included Seasonal allergy (Spring Allergies). On 18-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 18-Dec-2021, the patient experienced MALAISE (felt a little mild, like you don't have to think a lot.), DISCOMFORT (just a little uncomfortable), VACCINATION COMPLICATION (grade 4 side effects), MOBILITY DECREASED (She was unable to get up and make any food for herslef), VISUAL IMPAIRMENT (She also could not see straight when pouring her kettle of water.), ILLNESS (She lied in bed up through the entire day yesterday), PYREXIA (fever), MYALGIA (muscle pain /aches), HEADACHE (headache), FATIGUE (Her whole body loosened up, like you just came out of anesthesia or like her body was out of power,She was unable to get up and make any food for) and INTERCHANGE OF VACCINE PRODUCTS (She had received a primary vaccine series of the Pfizer covid-19 vaccine and received a booster dose of the Moderna covid-19 vaccine). On an unknown date, the patient experienced GAIT DISTURBANCE (could not walk / difficult task to get to the bathroom), INSOMNIA (did not sleep in 30 hours), ASTHENIA (no energy to be siting more than 30 minutes), BURNING SENSATION (entire body was burning for 30 hours) and CHILLS (shivers). On 18-Dec-2021, INTERCHANGE OF VACCINE PRODUCTS (She had received a primary vaccine series of the Pfizer covid-19 vaccine and received a booster dose of the Moderna covid-19 vaccine) had resolved. At the time of the report, MALAISE (felt a little mild, like you don't have to think a lot.), DISCOMFORT (just a little uncomfortable), VACCINATION COMPLICATION (grade 4 side effects), MOBILITY DECREASED (She was unable to get up and make any food for herslef), VISUAL IMPAIRMENT (She also could not see straight when pouring her kettle of water.), GAIT DISTURBANCE (could not walk / difficult task to get to the bathroom), INSOMNIA (did not sleep in 30 hours), ILLNESS (She lied in bed up through the entire day yesterday), ASTHENIA (no energy to be siting more than 30 minutes), BURNING SENSATION (entire body was burning for 30 hours), MYALGIA (muscle pain /aches), FATIGUE (Her whole body loosened up, like you just came out of anesthesia or like her body was out of power,She was unable to get up and make any food for) and CHILLS (shivers) outcome was unknown, PYREXIA (fever) had resolved and HEADACHE (headache) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 18-Dec-2021, Body temperature: 38 (High) temperature was round 38C.. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient took medication for spring allergy No treatment medication was reported by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 22-Dec-2021: Follow up received contain reporter's details, asthenia, Insomnia, chills, burning sensation, gait disturbance as event, spring allergies as medical history and small bowl obstruction as procedure has been updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: Test Date: 20211218; Test Name: Body temperature; Result Unstructured Data: temperature was round 38C.
Aktuelle Erkrankungen: Seasonal allergy (Spring Allergies)
Vorgeschichte: Medical History/Concurrent Conditions: Bowel obstruction surgery (small bowel obstruction); Small bowel obstruction
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1979167

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MD
Alter: 73,0
Geschlecht: M
Eingang: 24.12.2021
Impfdatum: 16.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 COVID-19 pneumonia Cough Hypoxia Pyrexia SARS-CoV-2 test positive

Symptomtext

Patient presented to the emergency department with complaints of hypoxia, cough, fever who tested positive for COVID-19. He was subsequently admitted to for management of COVID pneumonia. He was discharged to a group home in stable condition 5 days later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19 pneumonia
Hospital-Tage: 5,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1971322

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: IN
Alter: 24,0
Geschlecht: F
Eingang: 22.12.2021
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

Heart rate increased Loss of personal independence in daily activities Migraine Pain Pyrexia

Symptomtext

fever of 102 degrees, elevated heartrate (resting ~85), severe aches and pains all over body, long-lasting migraine, unable to perform usual daily tasks for two days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: Pfizer COVID-19 vaccine first dose (4/28/21) and second dose (5/19/21). Both of these vaccinations resulted in similar symptoms

VAERS 1963615

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

moderat

Staat: LA
Alter: 38,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 01.02.2021
Beginn: 12.05.2021
Tage bis Beginn: 100,0
Dosis: 3
Route/Site: IM / RA

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

Blood folate normal Blood test normal Borrelia test negative C-reactive protein normal Differential white blood cell count normal Feeling cold Full blood count normal Hypoaesthesia Hypoaesthesia oral Paraesthesia Red blood cell sedimentation rate normal Vitamin B12 normal

Symptomtext

Following the first dose, I had experienced facial coldness/numbness in my cheeks and nose on 3 occasions including on 3/12/2021. The sensation went away. On 11/18/2021 I got my booster shot and 12/1 I started to feel the sensation of a cold face again. The sensations moved to primarily the left side. My tip of my tongue is numb, and sometimes the two front teeth area. The sensation will sometimes not begin to later in the day and will continue for the remainder of the day until I go to sleep. Sometimes the sensations are helped by: warm bath and pressure. There are some days the sensations go away, but then return. On 12/19/2021 I started feeling numbness/tingling in the palm of my hands.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: 12/7: B Burgdorferi-Neg, Vitamin b12-normal, Folate-normal, sedimentation rate-normal, c-reactive protein-normal, CBC w Auto Differential-normal, Metobolic panel-Normal MRI w/wo contrast scheduled on January 14, 2022
Aktuelle Erkrankungen: None
Vorgeschichte: Migraines Eczema Lichen Sclerosis
Andere Medikamente: Buspar 10 mg 2X a day, Vitamin C, Vitamin D
Allergien: Amoxycillin
Vorherige Impfungen: -

VAERS 1963409

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MA
Alter: 52,0
Geschlecht: F
Eingang: 20.12.2021
Impfdatum: 18.12.2021
Beginn: 18.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Condition aggravated Decreased appetite Fatigue Headache Injection site pain Mobility decreased Myalgia Pyrexia

Symptomtext

My scheduled appointment was 2:30pm on Dec 18 2021, but I arrived earlier due to the snow storm, so the pharmacist gave me the shot around 12:15pm (the first person of the day received the vaccine in that store). In the afternoon, I felt a bit tired, mild reaction, then around 11:00pm when I went to bed, I started to have fever, headache, muscle pain (the whole body), injection site pain, too, extremely tired, the symptoms get more severe by the hour, grade 3-4. On Sunday 19th/Dec, I was in the bed for the entire day because of the exhaustion, fever and headache, which lasted 30 hours till Monday (20th) morning, at which point I began to feel myself. During the first 24-48 hours, I drank 1.5 gallon water, and ate very little. I even didn't have the energy to take a shower till this morning (20th).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: None, I didn't take any medication, but I reported to my GP.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None or I am not aware of. I suffered terrible AE from Pfizer vaccine after the 2nd shot on May 21 2021. On 18th of Dec 2021, I received Moderna booster shot with 0.25mL (50ug), experienced similar AE: fever, headache, entire body muscle pain, and tiredness (exhaustion), which sustained for 30 hours.
Vorherige Impfungen: Pfizer Vaccine 2nd dose on May 21 2021 Lot: EW0185.

VAERS 1961989

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: TN
Alter: 64,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 16.12.2021
Beginn: 17.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal discomfort Dehydration Fatigue Migraine Ocular discomfort Pollakiuria Vaccine positive rechallenge Vision blurred Visual impairment

Symptomtext

Moderna COVID-10 Vaccine EUA Dec 17: Migraine type headache centered around eyes. Need to urinate every half hour to hour causing dehydration. Upset stomach. Extremely tired. Drank as much water as I could hold which of course increased trips to the bathroom. Unable to focus eyes. Dec 18: Situation improving. Able to eat. Headache reduced to very heavy pressure around eyes. Sight returned to normal. Trips to bathroom down to once every 2 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: arthritis
Andere Medikamente: none
Allergien: antibiotics, latex, perfume, lanolin, adhesive tape, maltodextrin, cigarette smoke, caffeine
Vorherige Impfungen: Similar problems with first and second Moderna vaccine but not as severe.

VAERS 1958242

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: NY
Alter: 82,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 17.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / RA

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

Abdominal pain upper Dizziness Enterocolitis haemorrhagic Illness Mobility decreased

Symptomtext

Hemorrhaging colitis,started hemorrhaging; so sick; They could hardly walk; Felt like almost collapsing; Had stomach ache; This case was received via an unknown source (no reference has been entered for a health authority or license partner) on 07-Dec-2021 and was forwarded to Moderna on 07-Dec-2021. This spontaneous case was reported by a physician and describes the occurrence of ENTEROCOLITIS HAEMORRHAGIC (Hemorrhaging colitis,started hemorrhaging) in an 82-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Diabetes, Drug allergy (Aspirin) and Latex allergy. On 17-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In November 2021, the patient experienced ABDOMINAL PAIN UPPER (Had stomach ache). On 17-Nov-2021, the patient experienced ENTEROCOLITIS HAEMORRHAGIC (Hemorrhaging colitis,started hemorrhaging) (seriousness criteria hospitalization and medically significant), ILLNESS (so sick), MOBILITY DECREASED (They could hardly walk) and DIZZINESS (Felt like almost collapsing). The patient was hospitalized from 17-Nov-2021 to 22-Nov-2021 due to ENTEROCOLITIS HAEMORRHAGIC. The patient was treated with METRONIDAZOLE (intravenous) for Adverse event, at an unspecified dose and frequency and CIPROFLOXACIN (intravenous) for Adverse event, at an unspecified dose and frequency. At the time of the report, ENTEROCOLITIS HAEMORRHAGIC (Hemorrhaging colitis,started hemorrhaging), ILLNESS (so sick), MOBILITY DECREASED (They could hardly walk), ABDOMINAL PAIN UPPER (Had stomach ache) and DIZZINESS (Felt like almost collapsing) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. It was reported that patient administered 2 IV antibiotics (metronidazole and ciprofloxacin) along with fluids. Patient reported that she became so sick, could hardly walk, felt like almost collapsing, and when went to bathroom, she started hemorrhaging about three and half hours after the vaccine around 4-4:40 pm. Then she went to ER and admitted to hospital for 6 days due to hemorrhaging colitis and she remained in bed after having treatment. Patient also inquires about the ingredients of the vaccine in case there is something to explain her symptoms and also is concerned about getting the second dose. Also mentioned about caller's spouse vaccination. Spouse's first dose was on 14Feb2021 and lot#002B, second dose was on 15Mar2021, lot#007M20A, and booster dose was on 17Nov2021, lot#033F21A and was tired after the second and booster dose. Company comment This case concerns a 82-year-old female patient with no relevant medical history reported, who experienced the serious unexpected event of enterocolitis haemorrhagic. The event occurred the same day after the first dose of mRNA-1273. The rechallenge was not applicable since only information about the first dose was disclosed. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This case concerns a 82-year-old female patient with no relevant medical history reported, who experienced the serious unexpected event of enterocolitis haemorrhagic. The event occurred the same day after the first dose of mRNA-1273. The rechallenge was not applicable since only information about the first dose was disclosed. The benefit-risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: Diabetes; Drug allergy (Aspirin); Latex allergy
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1956386

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: NC
Alter: 69,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 29.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Atrial fibrillation Electrocardiogram abnormal Palpitations

Symptomtext

Patient received a Moderna COVID-19 booster dose (0.25ml) on 11/29/2021. She stated for two weeks following the booster dose, she experienced a racing heartbeat. Ten days after the booster dose she went to the doctor, an EKG was performed and Afib was noted from the EKG. The racing heartbeat has now stopped as of 12/15/2021.

Weitere VAERSDATA-Felder

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

VAERS 1955612

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: VA
Alter: 28,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Asthenia Back pain Breast pain Chest pain Chills Diarrhoea Dizziness Dyspnoea Fatigue Headache Heart rate increased Hot flush Limb discomfort Nausea Oropharyngeal pain Pain Pain in extremity Sleep disorder

Symptomtext

15 minutes after my second dose of the COVID vaccine, I developed leg heaviness in bilateral legs and became extremely dizzy. On my way home from the hospital I received my vaccine from, I had to pull over on the side of the road as it felt like I was going to pass out. 6 hours post vaccine, about 9pm on 12/14/2021 I developed intense THROBBING, lower back pain that lasted for 14 hours straight. I had no relief and could not sleep the entire night as no position was comfortable. I developed a 102 temperature, nausea, vomiting, throbbing headache, heart rate was 125bpm, hot flashes, cold chills, diarrhea, sore throat, shortness of breath, chest pain. Today, 12/16/2021, I am still experiencing pain throughout my entire body, especially my bilateral calfs. I am weak, dizzy, fatigued, I still have chest pain all day, I am experiencing shooting pains down my right arm (the arm I received the vaccine in), I am experiencing shooting pains in my bilateral breasts, I am having deep throbbing pain in the tops of my feet. Prior to this, I was a completely healthy 28 year old that has had no issues of illness like this in the past. This vaccine has messed up my life and the vaccine is not for everyone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None, I already spent $5,000 in medical tests, ER visits, cardiology visits post my first COVID vaccine that caused chest pain, shortness of breath, dizziness, lightheadedness, chest tightness. The medical community is not listening to my symptoms/concerns and they recommended that I receive the second dose.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Dairy, gluten
Vorherige Impfungen: 6/19/2021, Pfizer COVID vaccine first dose, chest pain/chest tightness, shortness of breath, dizziness, lightheadedness. 27 year

VAERS 1951210

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: GA
Alter: 36,0
Geschlecht: M
Eingang: 15.12.2021
Impfdatum: 12.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Immediate post-injection reaction Mobility decreased Pain Vaccination site pain

Symptomtext

pain at vaccination site immediately, at rest pain level 3/10 when trying to move 10/10, then lost function of the arm few hours later, now 3 days later he cannot lift the arm at all, needs assistance to lift the arm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1942182

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: VA
Alter: 54,0
Geschlecht: F
Eingang: 11.12.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Computerised tomogram abdomen Computerised tomogram pelvis Computerised tomogram thorax Cough Dizziness Dyspnoea Fatigue Heart rate increased Pericardial effusion Tremor

Symptomtext

extreme tiredness, dizziness and body shakes for 3 days. The day after the vaccine a cough developed, which has progressively worsened to today (4 weeks later). CT scan on 12/9/2021 indicated pericardial effusion, Symptoms continue to include coughing, shortness of breath and increased heart rate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: CT scan of chest, abdomen and pelvis on 12/9/2021
Aktuelle Erkrankungen: breast cancer
Vorgeschichte: breast cancer
Andere Medikamente: Ibrance, Faslodex, Crestor, Synthroid
Allergien: none
Vorherige Impfungen: Sickness from Covid vaccine #2 lasted 5 days

VAERS 1939310

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: VA
Alter: 36,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 08.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Arthralgia Back pain Chills Feeling abnormal Feeling of body temperature change Headache Lymph node pain Lymphadenopathy Malaise Mobility decreased Musculoskeletal chest pain Pain Pain in extremity Pyrexia Vaccine positive rechallenge Visual impairment

Symptomtext

The next morning I felt very "under the weather" (feverish, extremely achy, headache, pain on left arm). As the day went on these symptoms got worse. Sever lower back and leg/hip pain, severe headache, right eye vision disturbance, left calf pain. At approximately 5:30 PM on 12/9/21 , I had to lay down due to how poor I felt. I shivered and couldn't get warm no matter what I did. At approximately 8:30 PM on 12/9/21, I finally stopped shivering but then was so hot it felt as though my blankets and pillows were "burning me" (but it was me that was so hot). That lasted until approximately 6:00AM on 12/10/21. These gave way to whole left side pain on 12/10/21 (left calf, left rib area, kind of through to my back and sever swollen left lymph nodes (which I understand can be normal) that even hurts for my shirt to touch the area. I do understand that some of these symptoms may be normal but I believe many are not. This exact same scenario happened with my 2nd Moderna shot on 3/24/21 as well and I was hoping that it would not be the same with the booster (I was wrong).

Weitere VAERSDATA-Felder

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

VAERS 1936052

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: VA
Alter: 26,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 08.12.2021
Beginn: 08.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Decreased appetite Dehydration Exposure during pregnancy Fatigue Morning sickness Pyrexia Sleep disorder Vomiting

Symptomtext

Pregnancy: (10 weeks; first trimester). Symptoms: extreme fever and dehydration, fatigue, vomiting (likely a form of extreme morning sickness due to dehydration and empty stomach due to lack of appetite). Unable to sleep due to waking every 2 hours to use restroom.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: N/A due to avoiding hospital bills.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Buspar, Pre-natal, Probiotic
Allergien: N/A
Vorherige Impfungen: -

VAERS 1935219

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21a

moderat

Staat: MD
Alter: 56,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Fatigue Injection site erythema Injection site induration Injection site mass Injection site swelling Nausea Pain Paraesthesia Peripheral coldness

Symptomtext

Left deltoid hard lump and nickel size red swelling at injection site December 6, 4pm. Left deltoid hard lump and quarter size red swelling at injection site with more pain December 7, 9am. Left deltoid hard lump and $0.50 size red swelling at injection site with increased pain and increased fatigue and nausea; left hand cold and tingling.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: UTI and a yeast infection 7 days ago.
Vorgeschichte: Diabetes , High blood pressure, asthma
Andere Medikamente: Allegra, Flonase, Culturelle Woman?s Probiotic, Hair, Skin & Nails supplement, Gummy Vitamins, Aleve
Allergien: Contrast iodine, Benicar, penicillin, Diflucan, generic valsartan
Vorherige Impfungen: Tetanus shot. Hard lump at injection site 1 month later. August 1993

VAERS 1932745

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: CT
Alter: 42,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 05.12.2021
Beginn: 05.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Arthralgia Axillary pain Dizziness Fatigue Injection site pain Migraine Myalgia Nausea Vomiting

Symptomtext

Severe fatigue, severe nausea, vomiting, joint pain, muscle ache, pain in armpit, injection site pain and dizziness and migraine. Symptoms were minor on the day of the vaccine but severe the following two days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hypo thyroid (hashimotos)
Andere Medikamente: Synthroid, multivitamin, vitamin c, b complex, omega 3
Allergien: None
Vorherige Impfungen: -

VAERS 1931375

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: NJ
Alter: 69,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 05.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / RA

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

Cough Frequent bowel movements Limb discomfort Pain Palpitations Vaccination site erythema Vaccination site induration Vaccination site pruritus Vaccination site swelling Vaccination site warmth

Symptomtext

increased bowel movements after the vaccine when she goes like 3 times a day; heart palpitations; could not lift her arm; pain; cough; hot on his right arm; itchy on his right arm; hard on his right arm; red on his right arm/red mark 2 in wide 1 in wide; very swollen area,/approximately 2 inch high and 3 in wide/raised; This spontaneous case was reported by a consumer and describes the occurrence of FREQUENT BOWEL MOVEMENTS (increased bowel movements after the vaccine when she goes like 3 times a day), PALPITATIONS (heart palpitations), LIMB DISCOMFORT (could not lift her arm), PAIN (pain) and COUGH (cough) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Flu in 2020. Concurrent medical conditions included Autoimmune deficiency syndrome (with MTHFH methyltetrohydrofolate reductase deficient and cant convert Vitamin B.), Gluten intolerance and Homocysteinemia. Concomitant products included THYROID, PREDNISOLONE ACETATE and FISH OIL (OMEGA 3 COMPLETE) for an unknown indication. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. In November 2021, the patient experienced VACCINATION SITE WARMTH (hot on his right arm), VACCINATION SITE PRURITUS (itchy on his right arm), VACCINATION SITE INDURATION (hard on his right arm), VACCINATION SITE ERYTHEMA (red on his right arm/red mark 2 in wide 1 in wide) and VACCINATION SITE SWELLING (very swollen area,/approximately 2 inch high and 3 in wide/raised). On an unknown date, the patient experienced FREQUENT BOWEL MOVEMENTS (increased bowel movements after the vaccine when she goes like 3 times a day), PALPITATIONS (heart palpitations), LIMB DISCOMFORT (could not lift her arm), PAIN (pain) and COUGH (cough). At the time of the report, FREQUENT BOWEL MOVEMENTS (increased bowel movements after the vaccine when she goes like 3 times a day), LIMB DISCOMFORT (could not lift her arm), PAIN (pain), COUGH (cough), VACCINATION SITE WARMTH (hot on his right arm), VACCINATION SITE PRURITUS (itchy on his right arm), VACCINATION SITE INDURATION (hard on his right arm), VACCINATION SITE ERYTHEMA (red on his right arm/red mark 2 in wide 1 in wide) and VACCINATION SITE SWELLING (very swollen area,/approximately 2 inch high and 3 in wide/raised) outcome was unknown and PALPITATIONS (heart palpitations) had not resolved. Co-suspect product included Pfizer with unknown batch number on unknown date. Patient reported that C reactive proteins levels were natural high for her. It was also reported that patient was on OTC medications. No treatment reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Autoimmune deficiency syndrome (with MTHFH methyltetrohydrofolate reductase deficient and cant convert Vitamin B.); Gluten intolerance; Homocysteinemia
Vorgeschichte: Medical History/Concurrent Conditions: Flu
Andere Medikamente: THYROID; PREDNISOLONE ACETATE; OMEGA 3 COMPLETE
Allergien: -
Vorherige Impfungen: -

VAERS 1924866

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: NJ
Alter: 30,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 01.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Anosmia Chest discomfort Chest pain Condition aggravated Interchange of vaccine products Joint stiffness Lip pain Lip swelling Pruritus Swollen tongue Urticaria

Symptomtext

I had COVID in late January 2021. I received my first two doses of the Pfizer vaccine in April 2021. The day after I received my Moderna booster, I woke up with painful, large and puffy lips, which has never happened to me before. Benadryl eased the symptoms. For the past 5 weeks, I have had incidences of severe and itchy hives about 4 times a week all over my body but mostly on my torso (sometimes on my hands and face), painful puffy lips about 4 times a week (sometimes on the same days, sometimes not), extremely painful chest tightness twice (once on 11/17 and once on 12/5), extremely painful knuckle joint tightness in my hands (for about a week, the week of 11/29), and occasionally a swollen tongue. Benadryl eases the symptoms and Claritin and Allegra do not have any noticeable effects. I have not found a way to ease the symptoms. I saw my primary care physician who referred me to an allergist and provided no treatment. I also lost my smell the day I received the vaccine (11/1) and it has mostly returned by about 11/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None known
Vorgeschichte: Several food intolerances, never diagnosed
Andere Medikamente: Vitamin C
Allergien: Allergy to monocryl
Vorherige Impfungen: I lost my smell with the 2nd dose of the Pfizer vaccine on 4/26/2021

VAERS 1923719

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: PA
Alter: 35,0
Geschlecht: F
Eingang: 05.12.2021
Impfdatum: 02.10.2021
Beginn: 04.10.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: SYR / LA

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

Bronchospasm Burning sensation Cardiac flutter Chest discomfort Cough Dyspepsia Dyspnoea exertional Fatigue Upper respiratory tract infection

Symptomtext

After receiving the COVID 19 vaccine (which was mandated as a military member), within 24 hours I felt extreme fatigue. By Tuesday early morning I had began having severe coughing fits that were dry and uncontrollable. I was also short of breath both while moving (going up a flight of stairs) and while sedentary at times and had instances where my heart felt like it was fluttering. My chest/lungs felt like a small child was sitting on them aside from the burning, raspy cough. I took several cough suppressants to minimize the symptoms but as the coughing fits were keeping me up at night I went to my primary care physician on 10/5/2021. The nurse practitioner and I went over my symptoms and I was diagnosed with severe bronchial spasms with the potential for an asthma diagnosis. Having no issues with breathing previously, I asked that we rule other things out like bronchitis or an infection. The coughing fits continued with cough suppressants not minimizing the symptoms. I was told if I had an upper respiratory infection there was not much that could be done and that I should return in 6-8 weeks if the symptoms persist. On 11/2/2021 I received the second dose of the vaccine (again due to the military mandate and my unit's deadline of being fully vaccinated by 12/2/2021), and experienced the same extreme fatigue. At this point, the symptoms still had not subsided so I scheduled another appointment for 11/19/2021. The nurse practitioner indicated that it could still be an upper respiratory infection, perhaps indigestion (with zero previous issues with indigestion), or if I was not better in a month that we needed to seriously consider asthma and that based on the timing of my symptoms it appeared that the vaccine was the culprit as I had exhibited none of the symptoms prior to these events. I was prescribed an albuterol inhaler to aid in the coughing fits and shortness of breath. We scheduled a follow up visit for mid January to complete the diagnosis. As of 12/5/2021 I still have the symptoms described above. I remain short of breath and even long conversations often put me out of breath despite being previously moderately healthy and fit- per military requirements. The cold air exacerbates the coughing fits.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea exertional
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: -
Andere Medikamente: Multivitamins
Allergien: No known allergies
Vorherige Impfungen: -

VAERS 1921176

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: GA
Alter: 57,0
Geschlecht: F
Eingang: 03.12.2021
Impfdatum: 04.10.2021
Beginn: 11.10.2021
Tage bis Beginn: 7,0
Dosis: 2
Route/Site: SYR / RA

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

Blepharospasm Blood pressure increased Blood test Cognitive disorder Computerised tomogram Condition aggravated Confusional state Dizziness Electrocardiogram Fatigue Head discomfort Laboratory test Migraine Muscle twitching Vaccination complication

Symptomtext

Extreme pain at injection site for the first week making it extremely difficult to sleep. On 10/11, left eye started twitching uncontrollably. This twitching was found on search to be a know side effect. Second dose on 11/1 resulted in extreme dizziness and a migraine headache that lasted over 2 days even with prescription migraine medication. Left eye twitch has gotten much worse and twitching has moved down into my mouth also. I have had extreme exhaustion and confusion, along with inability to follow conversations and coherently reply when asked questions. There is a constant fluttering feeling in the left side of my head and it never stops. Due to these symptoms increasing and being similar to the signs of a stroke, i was taken to the Emergency Room of a local hospital on 12/2 to be examined. I had a CT scan, an EKG and various blood tests. The ER staff have diagnosed me with a post vaccine reaction. The second dose of the Moderna vaccine was on 11/1 at the same store and was Lot # 033F21A, if the vaccine card is to be believed. The online records for store show different lot numbers for both injections.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: Blood work, EKG, CT and various other tests performed at facility on 12/2/21
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure which has increased since vaccinations have been forced on me. Now, I have a higher dose of medication for this condition.
Andere Medikamente: Diltiazem, armour thyroid, HCTZ, Meloxicam
Allergien: None
Vorherige Impfungen: -

VAERS 1917180

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: OH
Alter: 44,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 30.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Hyperhidrosis Paraesthesia Tachycardia

Symptomtext

Heavy and strong rapid heart beat, sweating, full body tingling lasted about 5 min

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: None. Called ambulance. They did readings and no high BP or heart attack findings.
Aktuelle Erkrankungen: 3week recovering from full knee replacement
Vorgeschichte: None
Andere Medikamente: Advil, aspirin, multi vitamin, estrone, b12 supplement, stool softener
Allergien: Wheat
Vorherige Impfungen: -

VAERS 1917119

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: IN
Alter: 48,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 30.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / RA

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

Arthralgia Back pain Chest discomfort Chest pain Diarrhoea Feeling abnormal Myalgia Nightmare Pyrexia

Symptomtext

Chest tightness and pain, severe muscle back and hip pain, feels like I've been run over or used for a trampolin all into 2nd day after shot. Horrific vivid continuous nightmares from first into 2nd night. Fever 1st through2nd night, diarrhea 2nd day after shot. I feel awful.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: No tests, no doctor visits yet
Aktuelle Erkrankungen: Seasonal allergies, skin allergies and infections
Vorgeschichte: Narcolepsy, skin allergies and infections
Andere Medikamente: Vitamin b12, venlafaxine hcl 37.5 mg one tablet at bedtime., 200mg modifinil twice daily, hydrocortisone 2.5% and mupirocin 2% ointment
Allergien: Latex, omnicef, sulfa, tylenol, any antidepressant on prosac spectrum, cephalexin, most soaps and cleaning products cause rashes and skin infections
Vorherige Impfungen: Influenza

VAERS 1917072

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: IL
Alter: 31,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / RA

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

Chest pain Dizziness Fatigue Pain in extremity Palpitations Tachycardia

Symptomtext

Sore arm, fatigue, dizziness, heart palpitations, tachycardia, chest pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Aortic valve stenosis, bicuspid aortic valve, hashimotos
Andere Medikamente: Metoprotol, Levothyroxine
Allergien: Penicillin, Bananas
Vorherige Impfungen: -

VAERS 1916661

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: SC
Alter: 46,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Hypoaesthesia Immediate post-injection reaction Mobility decreased Pain in extremity

Symptomtext

Patient reports filling numbess in left arm immediately after vaccination. Progressed to having severe pain in arm, and inability to move arm later that night. The following morning, patient stated she couldn't move arm and was experiencing severe pain despite taking ibuprofen.

Weitere VAERSDATA-Felder

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

VAERS 1916539

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MO
Alter: 75,0
Geschlecht: M
Eingang: 02.12.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SC / RA

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

Asthenia Fatigue Injection site erythema Injection site swelling Mobility decreased Pyrexia Speech disorder Tremor

Symptomtext

Patient inadvertently received 3rd dose of COVID-19 vaccination. He had received 1 dose of Pfizer COVID-19 vaccination on 6/21/21 prior to facility admission. He received what was thought to be 1st dose of COVID-19 vaccination on 10/19/21. Following administration of what was thought to be 2nd dose on 11/19/21, it was discovered that he had 1 dose prior to admission. The 3rd vaccination resulted in mild fever 100.1, erythema & swelling at injection site, shakiness, weakness, fatigue, slowness with mobility & verbalizations starting about 12-18 hours after vaccination, but systemic effects resolved in 24-36 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: -
Labordaten: None, resolved in another 24-36 hours except mild injection site erythema, redness, & soreness which resolved in another 2-3 days, used cold packs on injection site intermittently and PRN Acetaminophen for injection site discomfort.
Aktuelle Erkrankungen: UTI 1 month prior.
Vorgeschichte: h/o PE;CKD Stage 3; Schizophrenia; Type 2 DM; Hypothyroidism; Hyperlipidemia; ASHD; GERD; HTN; BPH; overactive bladder.
Andere Medikamente: Acetaminophen; Ariprazole; ASA; Atorvastatin; Bupropion ER; Carvedilol; Eliquis; Finasteride; Hydralazine; Lamotrigine; Lantus; Levothyroxine; Lisinopril; MVI; Miralax; Novolog; Oxybutynin ER; Pantoprazole; Tamsulosin.
Allergien: NKDA.
Vorherige Impfungen: -

VAERS 1913076

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: NY
Alter: 32,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 13.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 17,0
Dosis: 1
Route/Site: - / -

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

Hypoaesthesia Injection site pain Pain in extremity Paraesthesia

Symptomtext

Tingling and numbness in both hands and feet, sharp pains in the top of the foot, and pain at injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None.
Vorgeschichte: Asthma.
Andere Medikamente: None.
Allergien: Peaches.
Vorherige Impfungen: -

VAERS 1912793

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

moderat

Staat: CA
Alter: 76,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Asthenia Chills Fatigue Hypertension Lethargy Pyrexia

Symptomtext

Systemic: Chills-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fever-Severe, Systemic: Hypertension-Severe, Systemic: Weakness-Severe

Weitere VAERSDATA-Felder

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

VAERS 1912783

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: NY
Alter: 35,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Condition aggravated Diarrhoea Dizziness Headache Interchange of vaccine products Loss of personal independence in daily activities Mobility decreased Myalgia Pyrexia Vaccination site erythema Vaccination site swelling Vaccination site warmth

Symptomtext

Dizziness, Fever, Chills, Diarrhea, Muscle Aches, Headache; Large, Hot, Red, Raised area (circle) around vaccination site. Started with Dizziness around 7 am on 11/5/21; progressed to a 102.3 fever, chills, and headache lasting until 11am on 11/6/21. Unable to continue daily activities, had to stay in bed.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Type 1 Diabetes (33 years), Hoshimotos Hypothyroidism
Andere Medikamente: Novolog, Labetalol, Vit D3, Venlafaxine, Lisinopril.
Allergien: Sulfa Drugs
Vorherige Impfungen: Pfizer; 2nd Dose: 3/10/21; Headache, Fever, Chills, Body Aches

VAERS 1909803

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: NC
Alter: 70,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Dyspnoea Fatigue Muscular weakness Pain Vision blurred

Symptomtext

Shortness of breath, weakness, blurred vision, tiredness, generalized aches and pains, legs are tired

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: none so far
Aktuelle Erkrankungen: none
Vorgeschichte: high blood pressure
Andere Medikamente: blood pressure meds; aspirin 81mg
Allergien: no allergies
Vorherige Impfungen: -

VAERS 1906720

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

moderat

Staat: GA
Alter: 74,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 28.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chills Feeling abnormal Feeling cold Insomnia Myalgia Pain Tremor

Symptomtext

Began about 9:30PM shaking chills, muscle aches, cold, temp 99.1. Today 11/29/21 still feeling bad, no energy, body aches and chills. Couldn't sleep. Woke up at 3:30 AM on 11/29/21, unable to sleep due to shaking chills, aches. Just don't feel good.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: Diabetes HTN
Andere Medikamente: Metformin ER 500mg BID, Olemsartin HCTZ
Allergien: PCN keflex Clindymycin
Vorherige Impfungen: Moderna 2nd shot, chills, body aches, no energy

VAERS 1905440

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: VA
Alter: 63,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 02.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Back pain Bacterial test Central venous catheterisation Computerised tomogram Differential white blood cell count Full blood count Magnetic resonance imaging Mobility decreased Purulence Spinal cord infection Spinal cord operation Staphylococcal infection Staphylococcus test positive

Symptomtext

One week later, on November 9th, 2021, I woke up with extreme pain in my lower back. I was rush to the hospital that evening, I could not go from a sitting position to a standing position. I was diagnosed with a staph infection in my spinal canal that extended from L2, L1, T12, T11 and T10. I was rushed in to EMERGENCY SURGERY on November 12, 2021, to remove the pus and staph from my spinal canal. The blood cultures came back positive for Staph - NO MRSA. I was sent home from the hospital on Tuesday Nov 16th, 2021, after insertion of a PICC line, and am currently on IV Cefazolin infusion at home, every 8 hours for the next 8 weeks.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mobility decreased
Hospital-Tage: 7,0
Labordaten: Cat Scan, 2 MRI's, multiple CBC with differential and multiple BLOOD CULTURES to determine the bacteria in my blood.
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: Multi Vitamin, B complex, A, C and D
Allergien: allergic to Demerol and Codine and Lobster
Vorherige Impfungen: -

VAERS 1905066

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A?

moderat

Staat: -
Alter: 68,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 19.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / LA

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

Dyspnoea Extra dose administered Flushing Injection site erythema Pain

Symptomtext

After booster dose pt had trouble breathing, large red area at injection site, body aches, facial flushing- had to take benadryl

Weitere VAERSDATA-Felder

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

VAERS 1904078

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MD
Alter: 37,0
Geschlecht: M
Eingang: 27.11.2021
Impfdatum: 01.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 3,0
Dosis: 1
Route/Site: IM / RA

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

Acoustic stimulation tests Ageusia Anosmia Blood pressure increased Blood test Confusional state Crying Dizziness Hyperacusis Palpitations Tearfulness Tinnitus

Symptomtext

Acute episode 11/4/21-11/5/21 (18-24 hours): sudden onset of dizziness, confusion, involuntary tearfulness/crying, lost taste/smell, tinnitus Chronic symptoms since 11/4/21: tinnitus, hearing sensitivity, dizziness New symptoms since 11/24/21: heart palpitations, elevated blood pressure

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: Scheduled tests: - 11/29/21 - hearing test - 11/30/21 - blood work + hospital testing
Aktuelle Erkrankungen: -
Vorgeschichte: high blood pressure
Andere Medikamente: atenolol 25 mg q.d.
Allergien: -
Vorherige Impfungen: -

VAERS 1897301

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: NY
Alter: 32,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 20.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Extra dose administered Herpes simplex

Symptomtext

HSV1 outbreak 2 days after receiving Covid booster shot. Diagnosed/initial outbreak in 08/2021 with no recurrence until receipt of the booster shot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: HSV1
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1893878

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: OH
Alter: 80,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 07.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Chills Diarrhoea Fatigue Headache Lymphadenopathy Nausea Oropharyngeal discomfort Pyrexia Tremor

Symptomtext

It started that evening with chills, headache, and shaking. I had a 101.6 fever. I had nausea. On Wednesday, I had diarrhea and fatigue. These symptoms lasted for about 5 days. I went to see the doctor to make sure that there was nothing was wrong. She gave me medicine for the diarrhea. Then, I got swollen lymph nodes in my groin area. When I went to the doctor, I did feel like something was in my throat. Now it in 2 weeks, I still have period of nausea. The lymph nodes have gone down.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: Congestive Heart Failure Asthma
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 1893770

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: SC
Alter: 32,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Burning sensation Neurological symptom Pain Paraesthesia Pruritus

Symptomtext

Received booster (3rd dose) on Friday Nov. 19th 2021 When waking up on Saturday Nov. 20th 2021 I immediately noticed neurological symptoms Stinging/Tingling/Burning/Itching "pins and needles" all over my body especially in my hands and feet These symptoms lasted for ~24 hours and then slowly tapered off. I have largely recovered although I still notice very slight tingling occasionally in my extremities.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: After Vaccine to treat symptoms Ibuprofen (dosage 800mg 1-2 times day) Acetaminophen (dosage 1000mg 1 time per day)
Allergien: -
Vorherige Impfungen: Looking back on this event I believe I experienced the same issues with my previous Covid vaccines although to a much milder deg

VAERS 1891641

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

moderat

Staat: MN
Alter: 22,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Dizziness Feeling hot Flushing Hyperhidrosis Tremor

Symptomtext

Systemic: Dizziness / Lightheadness-Severe, Systemic: Flushed / Sweating-Medium, Systemic: Shakiness-Mild, Systemic: Weakness-Mild, Additional Details: Patient said she felt dizzy, hot, weak, lightheaded about 5-10 mins post vaccination. Her hands were shaking and she looked sweaty. This lasted about 5 minutes. She remainded seated a while longer, then said she felt better and left.

Weitere VAERSDATA-Felder

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

VAERS 1890312

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: PA
Alter: 49,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 07.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / -

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

Chills Contusion Dizziness Fatigue Headache Hypoaesthesia Palpitations Peripheral swelling Pruritus Pyrexia Rash

Symptomtext

Dizziness, heart palpation, fever, chills, fatigue, headache, swollen arm, extreme itchiness, bruising, numbness, huge rash

Weitere VAERSDATA-Felder

Praegender Schweregrund: Palpitations
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: WPW, CHF, Asthma and diabetes
Andere Medikamente: None
Allergien: Vicodine
Vorherige Impfungen: Moderna dose 1

VAERS 1880750

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: IN
Alter: 79,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 15.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Body temperature increased Dyspnoea

Symptomtext

Patient c/o temperature of 101 the night after her vaccination. Patient also c/o of shortness of breath for 30 or 40 minutes the evening after vaccination. Patient stated symptoms resolved the following day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: no
Vorgeschichte: Diabetes Chronic Kidney disease
Andere Medikamente: unknown
Allergien: no
Vorherige Impfungen: -

VAERS 1879867

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: IA
Alter: 62,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 03.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / RA

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

Back pain Chest pain Insomnia Mobility decreased Nausea Pain SARS-CoV-2 test Swelling Ultrasound scan

Symptomtext

It becomes unbearable and jumps out of bed; pain in the back/it was getting worst/I'm having this pain and I thought it was gold Blatter/I had that kind of pain when had my gold Bladder stone; couldn't sleep since got the shot from the pain; in the arm pit area is swollen/something swollen up; if don't keep the arm prompt up it becomes very acute; nauseated; Chest pain; This spontaneous case was reported by a consumer and describes the occurrence of CHEST PAIN (Chest pain), PAIN (It becomes unbearable and jumps out of bed), BACK PAIN (pain in the back/it was getting worst/I'm having this pain and I thought it was gold Blatter/I had that kind of pain when had my gold Blatter stone), INSOMNIA (couldn't sleep since got the shot from the pain) and SWELLING (in the arm pit area is swollen/something swollen up) in a 62-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Gallstones (Gold bladder stone), Cancer surgery and Knee surgery NOS (total knee replacement).Concurrent medical conditions included Pulmonary embolism (on right lung), Blood pressure, Thyroid disorder, COPD, Clot blood (Genetic mutation for blood clotting in the lungs), Neuropathy and Arthritis.Concomitant products included APIXABAN (ELIQUIS) for Clot blood, FOLIC ACID (FOLIC) for Clotting disorder, GABAPENTIN and OMEPRAZOLE (PROTONIX [OMEPRAZOLE]) for an unknown indication.On 03-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 03-Nov-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced CHEST PAIN (Chest pain). On an unknown date, the patient experienced PAIN (It becomes unbearable and jumps out of bed), BACK PAIN (pain in the back/it was getting worst/I'm having this pain and I thought it was gold Blatter/I had that kind of pain when had my gold Blatter stone), INSOMNIA (couldn't sleep since got the shot from the pain), SWELLING (in the arm pit area is swollen/something swollen up), MOBILITY DECREASED (if don't keep the arm prompt up it becomes very acute) and NAUSEA (nauseated). The patient was treated with MORPHINE for Adverse event, at a dose of 4 unit, more. At the time of the report, CHEST PAIN (Chest pain) and PAIN (It becomes unbearable and jumps out of bed) had not resolved and BACK PAIN (pain in the back/it was getting worst/I'm having this pain and I thought it was gold Blatter/I had that kind of pain when had my gold Blatter stone), INSOMNIA (couldn't sleep since got the shot from the pain), SWELLING (in the arm pit area is swollen/something swollen up), MOBILITY DECREASED (if don't keep the arm prompt up it becomes very acute) and NAUSEA (nauseated) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available):On an unknown date, SARS-CoV-2 test: negative (Negative) Negative around July 26th.On an unknown date, Ultrasound scan: normal (normal) see the liver and looked for abnormalities and they didn't find anything.For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient had underwent lot of tests and blood clot test and results were unknown.Concomitant medication include Blood pressure pills, Protonix for the stomach, Thyroid medicine, Procyon 3 a day for neuropathy, Fariba and another unknown medicine for COPD. Treatment medication include muscles relaxants and injection of long lasting steroids, Something for the nausea,4 more units of morphine and an injection of long lasting steroids.Within an hour of vaccination the patient started to have like chest pain and then it shifted to the back. Went to the chiropractor and adjusted the back and did nothing to the pain. The next morning went to the emergency room because it was getting worst, did a lot of tests and blood clot test. The patient stated I'm having this pain and I thought it was gall bladder and they did a sonar scan and went to see the liver and looked for abnormalities and they didn't find anything. The patient then stated that in a scale of pain I'm on a 9 or 10. The patient also said that discovered that being laid in bed is excruciating because it pushes. There was only one position and was very weird because you have to lay down to the right side and put the entire arm under the body and reduces the pain from a 9 or 10 to a 7 when do that. It becomes unbearable and jumps out of bed. Guesses that there was something swollen up and in the arm pit area was swollen and said that if don't keep the arm prompt up it becomes very acute. The patient also mentioned that felt nauseated. The patient said that went all the way through the weekend like that, couldn't sleep since got the shot from the pain.This case was linked to MOD-2021-383210 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Test Name: COVID-19 Test; Test Result: Negative; Result Unstructured Data: Negative around July 26th; Test Name: Liver sonography; Result Unstructured Data: see the liver and looked for abnormalities and they didn't find anything.
Aktuelle Erkrankungen: Arthritis; Blood pressure; Clot blood (Genetic mutation for blood clotting in the lungs); COPD; Neuropathy; Pulmonary embolism (on right lung); Thyroid disorder.
Vorgeschichte: Medical History/Concurrent Conditions: Cancer surgery; Gallstones (Gold bladder stone); Knee surgery NOS (total knee replacement.)
Andere Medikamente: ELIQUIS; GABAPENTIN; FOLIC; PROTONIX [OMEPRAZOLE.]
Allergien: -
Vorherige Impfungen: -

VAERS 1876201

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: CA
Alter: 69,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Dizziness Hypoaesthesia Tremor Visual impairment

Symptomtext

Systemic: Chills-Mild, Systemic: Dizziness / Lightheadness-Mild, Systemic: Numbness (specify: facial area, extremities)-Mild, Systemic: Shakiness-Mild, Systemic: Visual Changes/Disturbances-Mild, Additional Details: patient was lightheaded, dizzy and had chills and was feeling like fainting so we called 911 and paramedics monitored her for 15 minutes they asked her if she wants to go to the hospital she refused because she started feeling better and they made her sign a conset that she can go home.

Weitere VAERSDATA-Felder

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

VAERS 1874435

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: PA
Alter: 29,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: SYR / LA

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

Chest discomfort Dyspnoea Electrocardiogram Heart rate increased Palpitations Sleep disorder Ultrasound scan

Symptomtext

heart palpitations, increased heart rate at rest, heart pounding in chest woke me twice during the night, chest tightness, labored breathing. I received the Moderna booster after initially receiving the Janssen vaccine on 03/19/2021; prescribed a beta blocker for heart palpitations and told to avoid aerobic exercise for two weeks and return to cardiologist for check up

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: Ultrasound and EKG completed on 11/12/2021
Aktuelle Erkrankungen: occasional migraines
Vorgeschichte: migraines, seasonal asthma
Andere Medikamente: junel fe birth control, sumatriptan 100mg, advil, multivatim
Allergien: Nut allergies, ciprofloxacin allergy, latex allergy
Vorherige Impfungen: -

VAERS 1873925

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MA
Alter: 66,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Heart rate increased Myalgia

Symptomtext

7 hours after injection I experienced full body muscle aches for approximately 18 hours. I also experienced elevated heart rates 3 days after the injection, up to 101 bpm for up to 3 days

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: No tests, only my checking my heart rate with my phone (heart rate app) and double checking that to that also has a continuous heart rate function,
Aktuelle Erkrankungen: -
Vorgeschichte: A-Fib
Andere Medikamente: Metoprolol 50mg 2/day Eliquis 5mg. 2/day Arimidex 1 mg. 1/day Gabapentin 100mg 1/day Zinc chelate w/vitamin C 2/day Vitamin D3 w/K2 1/day Magnesium chelate. 1/day Vitamin A 1/day
Allergien: Advil
Vorherige Impfungen: After Moderna vaccination?s 1 & 2 I also experienced elevated heart rates - up to 140 bpm. Both instances occurred approximate

VAERS 1872879

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MI
Alter: 41,0
Geschlecht: M
Eingang: 16.11.2021
Impfdatum: 12.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / LA

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

Condition aggravated Gout

Symptomtext

Gout flare up in right foot, big toe joint. Took colchicine and mobic at 10 PM on the same day which helped. Took a subsequent dose of the same in the morning.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Condition aggravated
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: IBS Gout
Andere Medikamente: Centrum Multivitamin
Allergien: -
Vorherige Impfungen: -

VAERS 1869278

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

moderat

Staat: MA
Alter: 47,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 31.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: SYR / RA

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

Arthralgia Asthenia Blood pressure increased Blood test normal Chest pain Chest scan Discomfort Headache Hypoaesthesia Inflammation Insomnia Interchange of vaccine products Neck pain Oedema peripheral Pain Pyrexia Swelling

Symptomtext

Got my first shot March 8 Janssen vaccine no reaction. On 10/31 got my booster shot Moderna and started with normal vaccine symptoms fever, weak, and had to rest afterI got home. On Nov 1 swelling of left side near neck. Uncomfortable. Nov 14 swelling continue to growth now both side neck, under arms, and groin. Left side more swelling than right side. Also numbness in left hand and left groin area. Pain that comes from the head to the next and continue to the elbow, and hand feels numb from time to time. Lack of sleep due to the pain left side and inflammation. ER 11/12 due to chest pain and pain neck.11/15 seek medical attention lack of primary care doctor and Sent me to the ER again.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chest pain
Hospital-Tage: -
Labordaten: Chest, and blood work came back okay. Blood pressure starting to lower. Pain in the neck - left side start from the head and go down to the elbow and hand feel numb. Left groin numb.
Aktuelle Erkrankungen: Asthma, but was control at time of vaccination.
Vorgeschichte: Asthma and high cholesterol- control at time of vaccination. Pre-diabetes.
Andere Medikamente: Vitafusion multivitamin for women, daily intake 2 gummy
Allergien: Chocolate and lime due to asthma
Vorherige Impfungen: -

VAERS 1869269

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: VA
Alter: 34,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Arthropathy Blood pressure increased Chest discomfort Chills Confusional state Dizziness Dyspepsia Dyspnoea Echocardiogram Electrocardiogram Heart rate irregular Injection site swelling Lethargy Musculoskeletal stiffness Palpitations Pyrexia Vision blurred

Symptomtext

06 NOV, 0430: woke with 102.4 degF fever; chills; stiff, popping joints; muscle stiffness; swelling in right arm at injection site. Took Tylenol. Resolved until mid-day. 06 NOV, 1230: frequent irregular heartbeats for multiple hours. Resting seemed to resolve. 07 and 08 NOV: frequent irregular heartbeats for multiple hours in the late afternoon to evening. Resting seemed to resolve. 09 NOV, late afternoon: Lethargy/deep fatigue; Lots of palpitations, several to five in a row of skipped beats; Light headed; Feels like weight on chest; Short of breath; Slight blurring of vision; Indigestion/belching; Some confusion/felt slow(?)/ needed to take notes; Left wrist pulsing a bit. Called cardiologist on-call. Went to ER, as I happened to be down there. BP was151/94, P79 (usually <130/<80, P70). EKG indicated possible left atrial enlargement. Could not get Echocardiogram that night. 10 NOV, 1100: followed up with Cardiology. Did EKG and Echo. Showed no variation from last year, but did not have measurements to determine enlargement, only pressure across conduit.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dyspnoea
Hospital-Tage: -
Labordaten: 09 NOV, evening: Went to ER, as I happened to be down there. BP was151/94, P79 (usually <130/<80, P70). EKG indicated possible left atrial enlargement. Could not get Echocardiogram that night. 10 NOV, 1100: followed up with Cardiology. Did EKG and Echo. Showed no variation from last year, but did not have measurements to determine enlargement, only pressure across conduit.
Aktuelle Erkrankungen: None
Vorgeschichte: Congenital Heart Disease Asthma Mild obesity/moderately overweight
Andere Medikamente: Singulair Centrum Specialist Heart Mucinex Allegra ?Baby? Aspirin
Allergien: Sulfa drugs Ceclor Toradol
Vorherige Impfungen: Already filed in VAERS

VAERS 1867569

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: PA
Alter: 26,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 10.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Asthenia Chills Decreased appetite Fatigue Flushing Hyperhidrosis Injection site pain Lethargy Muscle spasms Nausea Pain Pain in extremity Pyrexia Restlessness Tremor Vomiting

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Chills-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Fever-Medium, Systemic: Flushed / Sweating-Severe, Systemic: Nausea-Medium, Systemic: Vomiting-Medium, Systemic: Weakness-Medium, Additional Details: Pt received 2nd dose Moderna on 11/10 at 11am. Pt called 11/12 to report intense, significant adverse reactions that began 11/10 4pm & continuued thru 11/11. Pt described: sweating, chills, trembling, pain at injection site w no swelling, arm pain down to wrist, painful to raise arm above head, wrist cramp, arm ache & cramp, restlessness, nausea, vomitting several times. By Fri 11/12, pt states able to eat tea & banana, starting to feel better. Advised pt to drink water & resume eating.

Weitere VAERSDATA-Felder

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

VAERS 1864543

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

moderat

Staat: OK
Alter: 24,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Paraesthesia Paraesthesia oral Pruritus Tongue pruritus

Symptomtext

Systemic: Allergic: Itch (specify: facial area, extremeties)-Mild, Systemic: Tingling (specify: facial area, extemities)-Mild, Additional Details: Patient reported an itchy/tingling sensation on her tongue. Gave her water and 50mg of Benadryl and monitored for 30 minutes. She reported that it may have been nerves and "hyperchondriac" feeling. Patient was fine a few minutes later and for the duration of observation

Weitere VAERSDATA-Felder

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

VAERS 1864534

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: CA
Alter: 53,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 11.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Limb injury Pain Paraesthesia

Symptomtext

Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-

Weitere VAERSDATA-Felder

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

VAERS 1864533

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

moderat

Staat: TN
Alter: 42,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Hypoaesthesia 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, Systemic: Joint Pain-Severe, Systemic: Numbness (specify: facial area, extremities)-Severe, Systemic: Tingling (specify: facial area, extemities)-Severe, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Additional Details: according to patient, vaccine was administered by standing pharmacist. Vaccine was given too far forward and to the front of shoulder as opposed to in the deltoid

Weitere VAERSDATA-Felder

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

VAERS 1860667

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MO
Alter: 47,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain Asthenia Chills Fatigue Headache Injection site pain Insomnia Lethargy Mobility decreased Myalgia Pain Pyrexia

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Abdominal Pain-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Fever-Medium, Systemic: Headache-Medium, Systemic: Unable to Sleep-Medium, Systemic: Weakness-Medium, Additional Details: had fever 103F, stomach pain, unable to get out of bed, headache, muscle pain in arms and legs, fatigue. takes 2 capsules of advil every 4 hours to manage symptoms. fever/chills is now gone. adverse effects lasted 1 month after the first dose and 2 weeks after the second dose. pt states she has not seeked medical care for any of this and has not notified her provider. previously had covid march 2020 and was hospitalized 4 times. states benefit of vaccine outweighs risk for her.

Weitere VAERSDATA-Felder

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

VAERS 1858481

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

moderat

Staat: IN
Alter: 67,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Insomnia Migraine Pain in extremity Pyrexia

Symptomtext

100f fever, extremities ache, insomnia, huge pulsing migraine, started night of shot, still going up 27 by later.

Weitere VAERSDATA-Felder

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

VAERS 1857444

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: NY
Alter: 40,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 02.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / RA

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

Anxiety Decreased appetite Electrocardiogram normal Fatigue Feeling cold Headache Hypoaesthesia Insomnia Interchange of vaccine products Paraesthesia Peripheral coldness Psychiatric symptom Sensory loss Tremor

Symptomtext

This was a Covid Booster. I first received Janssen vax on 4/1/2021 and experienced a breakthrough Covid case on 8/2/2021. The day after the Moderna booster I felt typical covid vax side effects -- headache, exhaustion. On Saturday, 11/6, I started experiencing a dullness in my left hand and overall minimized sensation. Since then I've experienced general tingling, including arms, hands, legs and feet. I've had hours-long stretches of time where either hands or feet have been exceedingly cold but ultimately returned to normal. Additionally, I'm experiencing mildly shaky hands. I have a general feeling of disconnect and anxiety which in turn is leading to loss in appetite. Difficulty sleeping.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Paraesthesia
Hospital-Tage: -
Labordaten: Cardiology EKG and checked circulation to see if contributing to cold sensation. Tests normal. 11/9/2021.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1855560

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

moderat

Staat: VA
Alter: 62,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal discomfort Abdominal pain Chills Decreased appetite Diarrhoea Fatigue Headache Impaired work ability Migraine Mobility decreased Myalgia Nausea Photophobia Pyrexia Vomiting

Symptomtext

Fever 101, nausea/vomiting, abdominal pain, migraine, light sensitivity, lack of appetite, chills, muscle aches, upset stomach, diarrhea, severe headache , complete exhaustion, unable to work or get out of bed all day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Migraine
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Controlled minimal colitis
Andere Medikamente: Phenteramine. , Asacol
Allergien: Doxycycline
Vorherige Impfungen: -

VAERS 1849613

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: MA
Alter: 67,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Gait disturbance Headache Hypotension Myalgia Pain in extremity Pyrexia Sensitive skin

Symptomtext

Fever to 103, Severe headache Muscle pain Difficulty walking due to pain in my feet Skin hypersensitive Light headed on 2nd and 3rd day after shot Low blood pressure (94 systolic) on day 3 after shot Resolved with increased fluid intake in 2-3 hrs All symptoms resolved on 4th day after shot

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Praegender Schweregrund: Hypotension
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine Borderline hypertension
Andere Medikamente: Atenolol Atorvastatin Amitriptyline Multivitamin
Allergien: Aspirin Acetaminophen
Vorherige Impfungen: -

VAERS 1849242

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

moderat

Staat: TX
Alter: 49,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Arthralgia Joint injury Limb injury Paraesthesia

Symptomtext

Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-

Weitere VAERSDATA-Felder

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

VAERS 1848760

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

moderat

Staat: MO
Alter: 74,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Gait disturbance Headache Hypertension Myalgia

Symptomtext

AT 10 pm on 11/5, I had severe uncontrollable shivering for at least 1 hr. At 7 am on 11/6 I had severe headache, muscle pain in legs, unsteady upon walking, high blood pressure 160/76, pulse 106

Weitere VAERSDATA-Felder

Praegender Schweregrund: Hypertension
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: obesity, high BP, abnormal chest ct scan, moderate cerebral ischemia without infarction
Andere Medikamente: Losartan 50 mg, chlorthalidone 12-1/4 mg, 81 mg aspirin (x2), loratidine 10 mg, famotidine 20 mg., D3 1000 ICU, b-12 500 mg, doxycycline hyclate 100mg 2x./week
Allergien: All beta blockers lasix
Vorherige Impfungen: injection site redness, pain and rash lasting 3 days on 10/5/2021 on fluad; on moderna -arm pain and headaches

VAERS 1846641

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: VA
Alter: 56,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Asthenia Dehydration Dizziness Dizziness postural Epistaxis Eye contusion Fall Gait disturbance Joint injury Lip injury Nasal injury Pain Paraesthesia Poor quality sleep Skin abrasion Skin laceration

Symptomtext

Received the 2nd dose of Moderna approx 8:45 am on 11/4/21. Started feeling the tingly and achy side effects by about 7 pm that night. Went to bed feeling pretty achy and weak and had a somewhat restless sleep. Just before 5 am, our home fire alarms went off - my husband and I walked through the house to turn them off. On my way back upstairs, I started feeling very weak and dizzy. I stopped at the hall bathroom to use the bathroom. Upon standing up I was feeling incredibly weak and dizzy as if I was about to pass out. I grabbed the sink vanity and the door frame, and the next thing I remember is waking up on the floor with my husband who rushed to my side when he heard the thud of my body hitting the floor. I had a bloody nose, a gash on the bridge of my nose, a gash near my eyebrow, and a slightly split lip (all on my right side of face). Also scraped my elbow. Got back to bed with the help of my husband but felt like I could barely walk I was so weak. Also felt slightly dehydrated. Put a cold compress and ice on my face and rested for the next 6 hours. Will likely have a black eye and suspect I may possibly have broken my nose during my fall. NOTE: I was forced to get this vaccine in order to keep my job; I did not otherwise intend to get the vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dehydration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: Leiden Factor VI
Andere Medikamente: 81 mg aspirin
Allergien: none
Vorherige Impfungen: -

VAERS 1831820

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

moderat

Staat: TX
Alter: 76,0
Geschlecht: F
Eingang: 30.10.2021
Impfdatum: 28.10.2021
Beginn: 28.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Arthritis Asthenia Chills Diarrhoea Dizziness Headache Hyperhidrosis Injection site erythema Injection site pain Nausea Pain Pyrexia Retching Tremor

Symptomtext

About 12 hours after receiving vaccine all symptoms came on just about at once. Pain and redness in left arm, total body painful aches, pressure headache (the worst!) fever 100.5, increased joint pain (I have arthritis), chills to the point of total body shaking, nausea, dry heaves, dizziness, very very weak. No treatment sought. Went to bed and piled on the blankets. Slept and sweated. Next morning I had diarrhea when I experienced a large mudslide of fecal matter. Within the next two hours after that, the only symptoms remaining were weakness, injection site soreness and redness, and headache. I wish the headache would go away! And that is still my condition now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tremor
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: arthritis
Andere Medikamente: none
Allergien: Penicillin, aspirin, codeine, Clindamycin, prednisone, metronedazole, saccharomyces boulardi
Vorherige Impfungen: The same as reported above but so much less severe for only a few hours

VAERS 2512406

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NY
Alter: 31,0
Geschlecht: F
Eingang: 09.10.2023
Impfdatum: 11.03.2021
Beginn: -
Tage bis Beginn: -
Dosis: 2
Route/Site: SYR / UN

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

Alopecia Arthralgia Limb discomfort Pain Photopsia Circumstance or information capable of leading to medication error Feeling abnormal Malaise Rash SARS-CoV-2 test Vitreous floaters

Symptomtext

HER HAIR WAS FALLING OUT; SORENESS AND PAIN FROM THE VACCINE; HER CHEST WAS ALL RED LIKE SHE HAD A BAD RASH; HER SHOULDER WAS HURTING FOR TOO LONG; HER ARM WAS KILLING HER; VITREOUS FLOATERS; VITREOUS FLASHES; This spontaneous report received from a patient concerned a 4 decade old female. The patient's height, and weight were not reported. The patient's pre-existing medical conditions included: Patient had no known allergies. Patient does not have a prior history of eye problems nor heart conditions. The patient experienced cold symptoms when treated with influenza vaccine for prophylactic vaccination. The patient received covid-19 vaccine ad26.cov2.s (suspension for injection, intramuscular, batch number: 1805022 expiry: UNKNOWN) dose was not reported, administered on 11-MAR-2021 for covid-19 prophylaxis. Age at time of vaccination 31 years old. No concomitant medications were reported. On 2021, the patient experienced vitreous floaters, and vitreous flashes. On an unspecified date, the patient experienced her hair was falling out, soreness and pain from the vaccine, her chest was all red like she had a bad rash, her shoulder was hurting for too long, and her arm was killing her. Laboratory data (dates unspecified) included: COVID-19 virus test didn't have virus. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from vitreous floaters, and vitreous flashes, and the outcome of her chest was all red like she had a bad rash, soreness and pain from the vaccine, her hair was falling out, her shoulder was hurting for too long and her arm was killing her was not reported. This report was non-serious. This report was associated with product quality complaint 90000299490.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Malaise
Hospital-Tage: -
Labordaten: Test Name: COVID-19 VIRUS TEST; Result Unstructured Data: didn't have virus
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Patient had no known allergies. Patient does not have a prior history of eye problems nor heart conditions.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2640480

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: GA
Alter: 63,0
Geschlecht: F
Eingang: 03.06.2023
Impfdatum: 01.12.2021
Beginn: 10.12.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / LA

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

Angioedema Chronic spontaneous urticaria Laboratory test

Symptomtext

Adverse effect: Chronic Spontaneous Urticaria and Angioedema. (CSU/A). First informed it should last 3 months, then 6 months, then it may go into remission by Dr. As of current day still experiencing CSU/A. With medication of antihistamines, episode as recent as June 2, 2023, Angioedema episode.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chronic spontaneous urticaria
Hospital-Tage: -
Labordaten: Several test with at emergency at Hospital in 2022. Most recent 15 test with Dr.
Aktuelle Erkrankungen: Bunion surgery month before, booster Nov. 2021
Vorgeschichte: None prior to Moderna?s 1st Booster (3rd shot total).
Andere Medikamente: None at the time of vaccine.
Allergien: Sulfa, Benadryl, casting dye
Vorherige Impfungen: -

VAERS 2612507

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21A

mild

Staat: CT
Alter: 57,0
Geschlecht: M
Eingang: 10.04.2023
Impfdatum: 12.03.2021
Beginn: 13.03.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / RA

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

Rash Urticaria

Symptomtext

severe rash and hive everywhere but the face, come on around 1 to 2 pm daily, location does not matter in car walking sitting etc. Horrible !!!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Put on high dose of allergy med, little effect was then prescribed Zolair injections in both arms once a month, shots are $3000.00 per month. been taking them for 11 months, rash goe away while on Zolair but comes back when not on Zolair. Dr advised i no longer recieve the mrna vaccine due t o these adverse bull side effects.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2557619

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CA
Alter: 67,0
Geschlecht: F
Eingang: 11.01.2023
Impfdatum: 04.11.2021
Beginn: 07.11.2022
Tage bis Beginn: 368,0
Dosis: 3
Route/Site: SYR / LA

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

Fatigue Neuralgia

Symptomtext

I woke up on Sunday, 11/07/2021, feeling tired. A week or two later I started noticing a burning nerve pain sensation. I took TYLENOL and ADVIL to treat the symptoms. I may have mentioned it to my primary care doctor or the endocrinologist but it was never officially documented. The nerve pain was much more intense than the previous dose and it lasted for a longer duration of time than the previous dose. Right before I received the next booster, I had noticed an improvement in the nerve pain from before and actually felt "great".

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Hashimoto's Thyroiditis
Andere Medikamente: SYNTHROID; vitamin D every other week; clonidine; ZYRTEC
Allergien: Sulfa
Vorherige Impfungen: Dose 2 of Moderna: 1 day of feeling unwell 49 hours after receiving the vaccine and then weeks later experienced burning nerve s

VAERS 2515323

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MI
Alter: 75,0
Geschlecht: F
Eingang: 23.11.2022
Impfdatum: 08.12.2021
Beginn: 15.11.2022
Tage bis Beginn: 342,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Chest X-ray abnormal Chills Cough Hypoxia Lung hyperinflation Nasal congestion Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Urinary tract disorder Urinary tract infection Urine analysis abnormal

Symptomtext

Discharge Provider: , MD Primary Care Provider at Discharge: Admission Date: 11/15/2022 Discharge Date: 11/17/2022 COVID positive Date: 11/15/2022 PRESENTING PROBLEM: COVID-19 HOSPITAL COURSE: Patient is a 76 y.o. female, peripheral neuropathy, osteoarthritis, Barrett's esophagus, anemia and arthritis. She presented to a local hospital on 11/15/2022 with chills, nasal congestion, coughing, sore throat, runny nose x 3 days. The patient was found to be COVID positive upon admission to the emergency department with hypoxia requiring 3 L nasal cannula supplemental oxygen. Chest x-ray was performed and showed hyperinflated lungs without any infiltrates. While hospitalized the patient was treated with Decadron and remdesivir. She received a total of 2 days of treatment. Her hypoxia improved quickly with treatment and she will be returning home without additional skilled services. Will continue supportive care with scheduled Mucinex and p.r.n. Tessalon Perles upon discharge. The patient also complained of urinary symptoms and her urine was consistent with UTI. She was started on bactrim which will be continued upon discharge. Recommend outpatient follow-up with PCP in 1-2 weeks for post hospitalization follow-up and coordination of care.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: 2,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Primary hypertension Barrett's esophagus with dysplasia GERD with esophagitis S/P gastric bypass Acute cystitis Iron deficiency anemia secondary to inadequate dietary iron intake Lumbar radiculopathy Polyneuropathy Chronic pain of both ankles Generalized body aches Chronic pain syndrome Urinary incontinence Overweight Hiatal hernia Post-menopause Situational anxiety Framingham cardiac risk 10-20% in next 10 years Hypersomnia
Andere Medikamente: benzonatate (TESSALON) 200 MG capsule (Expired) clonazePAM (KLONOPIN) 0.5 MG tablet diclofenac sodium 1 % gel estradiol (ESTRACE) 1 MG tablet ferrous sulfate 325 (65 Fe) MG tablet gabapentin (NEURONTIN) 300 MG capsule guaiFENesin (MUCINEX)
Allergien: NKA
Vorherige Impfungen: -

VAERS 2508329

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MI
Alter: 69,0
Geschlecht: F
Eingang: 15.11.2022
Impfdatum: 03.06.2021
Beginn: 20.09.2022
Tage bis Beginn: 474,0
Dosis: 2
Route/Site: - / -

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

Animal bite COVID-19 Pain in extremity Peripheral swelling SARS-CoV-2 test positive

Symptomtext

09/20/22 presents to ED for "pain and swelling of left upper extremity" "cat bite". PMHx of "Afib, HTN, PUD, GERD"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: 09/21/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2507202

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: IL
Alter: 38,0
Geschlecht: F
Eingang: 14.11.2022
Impfdatum: 08.11.2021
Beginn: 15.09.2022
Tage bis Beginn: 311,0
Dosis: 3
Route/Site: SYR / AR

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

Arthralgia Grip strength decreased Motor dysfunction Pain Pain in extremity

Symptomtext

9/15/2022 I had been noticing trouble opening jars and pain in my hands and in my joints. My fine motor movements were harder. It has progressively gotten worse with an achy feeling. I confirmed with a migraine specialist that it is not related to migraines. I have an appointment with my PCP on 12/14/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Psoriasis
Andere Medikamente: Multivitamin; calcium plus D; super B complex; vitamin D; magnesium; fluoxetine; topiramate; bupropion; nortriptyline
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2497803

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 29,0
Geschlecht: F
Eingang: 03.11.2022
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Rash

Symptomtext

Developed rash all over torso 2 days after vaccine that lasted about 3 days. Took Benadryl for 1 or 2 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: Sulfa medications
Vorherige Impfungen: Moderna, first shot, Moderna bivalent

VAERS 2488264

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MI
Alter: 44,0
Geschlecht: F
Eingang: 25.10.2022
Impfdatum: 03.11.2021
Beginn: 13.12.2021
Tage bis Beginn: 40,0
Dosis: 3
Route/Site: SYR / LA

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

Asthma Blood test Cardiac stress test Chronic kidney disease Computerised tomogram thorax Echocardiogram Heart rate increased Urticaria Urticaria chronic Vocal cord inflammation

Symptomtext

Chronic hives/urticaria that have been persistent for 10 months. I developed asthma after my booster. I had increased heart rate for approx 7 months. I have inflation of my vocal chords that has been persistent. I developed chronic kidney disease.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: Multiple blood tests from May through current. CT scan of lungs in July 2022, ECHO and stress test October 2022.
Aktuelle Erkrankungen: none
Vorgeschichte: Hypothyroid
Andere Medikamente: Synthroid
Allergien: no
Vorherige Impfungen: -

VAERS 2458240

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: -
Alter: 57,0
Geschlecht: F
Eingang: 24.09.2022
Impfdatum: 29.09.2021
Beginn: 10.11.2021
Tage bis Beginn: 42,0
Dosis: 2
Route/Site: OT / -

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

Arthropathy Dizziness Fatigue Headache Injection site bruising Injection site erythema Injection site pruritus Musculoskeletal disorder

Symptomtext

Lower extremity dysfunction/Feet lasting for about an hour; Ankle arthropathy/Ankle lasting for about an hour; Dizziness; Injection site itching; Fatigue; Headache; Recurrent injection site bruising; Injection site bruising; Injection site itching; Injection site redness; This spontaneous case was reported by a consumer and describes the occurrence of INJECTION SITE BRUISING (Recurrent injection site bruising), MUSCULOSKELETAL DISORDER (Lower extremity dysfunction/Feet lasting for about an hour), ARTHROPATHY (Ankle arthropathy/Ankle lasting for about an hour), INJECTION SITE BRUISING (Injection site bruising) and DIZZINESS (Dizziness) in a 57-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product ADALIMUMAB (HUMIRA) for Rheumatoid arthritis. Previously administered products included for COVID-19 vaccination: COVID-19 VACCINE NRVV AD26 (Route of administration: Intra-muscular Batch number:041A21A) on 02-Apr-2021. Past adverse reactions to the above products included No adverse reaction with COVID-19 VACCINE NRVV AD26. On 29-Sep-2021, the patient started ADALIMUMAB (HUMIRA) (Subcutaneous) Citrate free. On 11-Nov-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 10-Nov-2021, the patient experienced the first episode of INJECTION SITE PRURITUS (Injection site itching) and INJECTION SITE ERYTHEMA (Injection site redness). On 11-Nov-2021, the patient experienced INJECTION SITE BRUISING (Injection site bruising). On 24-Nov-2021, the patient experienced INJECTION SITE BRUISING (Recurrent injection site bruising). On an unknown date, the patient experienced MUSCULOSKELETAL DISORDER (Lower extremity dysfunction/Feet lasting for about an hour), ARTHROPATHY (Ankle arthropathy/Ankle lasting for about an hour), DIZZINESS (Dizziness), the second episode of INJECTION SITE PRURITUS (Injection site itching), FATIGUE (Fatigue) and HEADACHE (Headache). On 10-Nov-2021, INJECTION SITE ERYTHEMA (Injection site redness) had resolved. In November 2021, INJECTION SITE BRUISING (Injection site bruising) had resolved. At the time of the report, INJECTION SITE BRUISING (Recurrent injection site bruising) was resolving, MUSCULOSKELETAL DISORDER (Lower extremity dysfunction/Feet lasting for about an hour), ARTHROPATHY (Ankle arthropathy/Ankle lasting for about an hour), the last episode of INJECTION SITE PRURITUS (Injection site itching), FATIGUE (Fatigue) and HEADACHE (Headache) had resolved and DIZZINESS (Dizziness) had not resolved. On 10 Nov 2021, the patient experienced removed cap 1 first followed by cap 2 without twisting/waited for 4 to 5 seconds before lifted the pen/ more medication end up on top of the injection site/received a partial injection(Wrong injection technique), fluid around injection site/unsure if got full dose/felt like pen did not fully inject/yellow flag all the way down(Inappropriate dose of drug administered) (Device issue) and outcome for the events was unknown. The reporter's causality for the event(s) of fatigue, dizziness, itching around injection site, headache, injection site redness and injection site itchiness with Humira 40MG/0.4ML(Adalimumab) was a reasonable possibility. the reporter's causality for the event(s) of feet lasting for about an hour, removed cap 1 first followed by cap 2 without twisting/waited for 4 to 5 seconds before lifted the pen/ more medication end up on top of the injection site/received a partial injection, fluid around injection site/unsure if got full dose/felt like pen did not fully inject/yellow flag all the way down onset 10 Nov 2021, fluid around injection site/unsure if got full dose/felt like pen did not fully inject/yellow flag all the way down onset 10 Nov 2021 and ankle lasting for about an hour was not provided. The reporter's causality for the event(s) of recurrent injection site bruising and injection site bruising with Humira 40mg/0.4ml(Adalimumab) was no reasonable possibility. This case was identified as part of a retrospective clean-up activity where certain emails received in the Moderna mailbox were missed to be booked-in. Most recent FOLLOW-UP information incorporated above includes: On 09-Dec-2021: Follow up report received and Added product and event information.

Weitere VAERSDATA-Felder

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

VAERS 2414746

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: TX
Alter: 82,0
Geschlecht: M
Eingang: 18.08.2022
Impfdatum: 16.02.2022
Beginn: 28.05.2022
Tage bis Beginn: 101,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Fatigue Nasopharyngitis SARS-CoV-2 test positive

Symptomtext

Started having a cold and felt really fatigued. Went and got tested for with a PCH COVID-19 test at urgent care and it was positive. Was prescribed meclizine for 7 days. Started feeling better. Had another COVID-19 PCH test - negative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: COVID-19 PCH test - positive, COVID-19 PCH test - negative.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Simvastatin; metoprolol; LEXAPRO; valsartan/hydrochlorothiazide; baby aspirin; ALLEGRA
Allergien: N/A
Vorherige Impfungen: -

VAERS 2411224

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CT
Alter: 74,0
Geschlecht: F
Eingang: 15.08.2022
Impfdatum: 19.11.2021
Beginn: 26.12.2021
Tage bis Beginn: 37,0
Dosis: 3
Route/Site: IM / RA

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

Blood test COVID-19 Dizziness Electroencephalogram normal Headache Vitamin D increased

Symptomtext

I had headaches for about 4 months after contacting COVID-19 in December of 2021 only on the right side of my head. I also experienced a feeling as if I was going to pass out or as if I was slightly intoxicated. That has persisted after COVID-19. Some days are good, and some days are bad in terms of having that feeling. Sometimes it lasts all day, sometimes I don't have it, sometimes I have it periodically. I recently followed up with my neurologist. I've had three ambulatory EEGs and they have not shown anything. I asked him what he thought, he said, the problem is that there is no real test for it. I thought it might be that I was dehydrated, but I am not. It doesn't seem to be related to physical position. So, I don't know what it is. I'm still being monitored by my neurologist and in January, I will have another EEG.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Multiple EEGs-04/08/2022-09/14/2022 and 06/02/2022-nothing found; Blood Panel-12/13/2021-High vitamin D levels.
Aktuelle Erkrankungen: Esophageal Spasm
Vorgeschichte: Epilepsy; Irritable Bowl Syndrome
Andere Medikamente: Depakote; Effexor ER; Dicyclomine; Crestor; Zinc; Multivitamin
Allergien: Tridone; Anti-nausea medications
Vorherige Impfungen: -

VAERS 2373922

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 68,0
Geschlecht: F
Eingang: 19.07.2022
Impfdatum: 03.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 28,0
Dosis: 3
Route/Site: SYR / LA

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

Biopsy skin abnormal Granuloma annulare Rash

Symptomtext

My 1st and 2nd vaccine was Pfizer with no adverse reaction. Within a month of receiving the Moderna booster vaccine, I developed a rash on my front upper thighs and elbows. Thinking it was just my skin's new reaction to my usual winter dry skin, I used a regular body lotion. I had a primary Dr. appointment on March 4 and the PA gave me a prescription for Betamethasone Dipropionate, which had no results. I called Dermatology and made an appointment for May 24, 2022. On that date, Dr. made a visual assessment of Granuloma Annulare and a biopsy confirmed that diagnosis. The rash is now on my arms, front and rear of my legs, buttocks, torso, and hands.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Punch biopsy, 5/24/22. Inflammatory dermatosis. Granuloma annulare
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: lisinopril 20mg; simvastatin 40mg; multi vitamin
Allergien: none
Vorherige Impfungen: -

VAERS 2362597

PFIZER\BIONTECH · COVID19 (COVID19 (PFIZER-BIONTECH)) · Charge 033F21A

mild

Staat: TX
Alter: 73,0
Geschlecht: F
Eingang: 08.07.2022
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: nein

Fatigue Insomnia Ultrasound abdomen

Symptomtext

Extreme fatigue and lack of sleep

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Abdominal Sonogram
Aktuelle Erkrankungen: NA
Vorgeschichte: Asthma
Andere Medikamente: Levothyroxine, Meloxicam, Advair as needed, Multi Vitamin, Zyrtec D
Allergien: NA
Vorherige Impfungen: -

VAERS 2315432

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 70,0
Geschlecht: M
Eingang: 10.06.2022
Impfdatum: 09.11.2021
Beginn: 02.06.2022
Tage bis Beginn: 205,0
Dosis: 3
Route/Site: SYR / LA

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

Abdominal pain COVID-19 Cough Influenza like illness Nasopharyngitis Pyrexia Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

On Thursday, the day it began. I felt a scratchy throat at work and a cough that I tried to suppress by drinking water. The next day, the cough felt like I was beginning to get the flu or cold. I took an at home test and it came back positive. The cough persisted and I went to sleep. The cough was a dry cough and a runny nose. Following that, I started getting sore around my belly and abdomen because of coughing so much. Saturday night I had a temperature at 101 at about 7pm and that lasted for about an hour. I had a good appetite and never lost my taste. No body aches, no diarrhea. Just the cough and runny nose and the fever that lasted for about an hour. Sunday, I began to come around. I never was down to the point where I had to be in bed, I just stayed in bed. And it was just like a flu. Contacted doctor on Friday as well and was prescribed the Paxlovid and started that medication that evening. Had to stop taking Rosuvastatin at this time so I could take Paxlovid.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: 06/03/2022-At Home COVID Test-Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Type 2 Diabetes; High blood pressure; Gout
Andere Medikamente: Metformin; JANUVIA; losartan; chlorthalidone; allopurinol; nebivolol; terazosin HCL; vitamin D; vitamin C; zinc; baby aspirin; rosuvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 2307067

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CA
Alter: 57,0
Geschlecht: F
Eingang: 02.06.2022
Impfdatum: 01.12.2021
Beginn: 26.04.2022
Tage bis Beginn: 146,0
Dosis: 3
Route/Site: IM / LA

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

Cough Fatigue Rhinorrhoea SARS-CoV-2 test

Symptomtext

Started with dry cough and then moved down into my chest. Then pretty significant fatigue the first two days. Then just croopy cough and runny nose and fatigue. I never had a fever. My symptoms April 26th, a Tuesday. The worst was about the 30th and then I began to feel better. As of today I am completely recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: At home nasal swab Covid test.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension
Andere Medikamente: Propranolol; fluoxetine; multivitamin; loratadine
Allergien: Neosporin; adhesive tape
Vorherige Impfungen: -

VAERS 2301380

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NJ
Alter: 62,0
Geschlecht: F
Eingang: 28.05.2022
Impfdatum: 04.05.2022
Beginn: 05.05.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / -

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

Back pain Dysstasia Gait inability Joint range of motion decreased Pain Pain in extremity

Symptomtext

Dose 1-Injection site pain - very, very, sore, swollen which lasted about 1 week, back pain near scapula, which lasted for three weeks, fever for two days. Dose 2- Injection site pain, fever, under arm lymph node pain for a week, weird back pain on entire back which lasted about a week. Dose 3- No side effects. Dose 4- Extreme lower back pain, across entire lower back and down both legs. I could not stand, could not walk, could not bend for three days. I had to lie flat for three days. The fourth day was a little better. By the fifth day I was almost back to normal. I will not get a 3rd booster. The 4th shot was too frightening and painful. I feared my ability to walk was gone. I am done with the vaccines!

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: MS, Seizure disorder
Andere Medikamente: Keppra, Vit B complex, Turmeric, Bone supplement, Magnesium, Cranberry caps
Allergien: -
Vorherige Impfungen: -

VAERS 2299611

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: -
Alter: -
Geschlecht: U
Eingang: 28.05.2022
Impfdatum: 08.11.2021
Beginn: 05.05.2022
Tage bis Beginn: 178,0
Dosis: 3
Route/Site: OT / LA

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

Diarrhoea Dysgeusia

Symptomtext

Severe metallic taste in mouth that maximized about 1.5-2hrs; Diarrhea over 2-3 days - soft then liquid; This spontaneous case was reported by a non-health professional and describes the occurrence of DYSGEUSIA (Severe metallic taste in mouth that maximized about 1.5-2hrs) and DIARRHOEA (Diarrhea over 2-3 days - soft then liquid) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. Co-suspect product included non-company product NIRMATRELVIR, RITONAVIR (PAXLOVID) for COVID-19 treatment. Previously administered products included for Product used for unknown indication: Pfizer (Dose Number: 1 Batch/Lot No: EL8982 Location of injection: Arm Left Vaccine Administration Time: 02:00 PM) on 19-Jan-2021 and Pfizer (Dose Number: 2 Batch/Lot No: EM9810 Location of injection: Arm Left Vaccine Administration Time: 02:00 PM) on 09-Feb-2021. Past adverse reactions to the above products included No adverse event with Pfizer and Pfizer. On 08-Nov-2021 at 10:00 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-May-2022, the patient started NIRMATRELVIR, RITONAVIR (PAXLOVID) (unknown route) at an unspecified dose. On 05-May-2022, the patient experienced DYSGEUSIA (Severe metallic taste in mouth that maximized about 1.5-2hrs) and DIARRHOEA (Diarrhea over 2-3 days - soft then liquid). On 10-May-2022, DYSGEUSIA (Severe metallic taste in mouth that maximized about 1.5-2hrs) and DIARRHOEA (Diarrhea over 2-3 days - soft then liquid) had resolved. It was reported that patient had no allergy. No Medical History information was reported. Concomitant medication reported as Nature made started on 01-Mar-2022 and stop date reported as 20-May-2022. The stop date was reported as 08-NOV-2021 for Moderna COVID-19 Vaccine. It was reported that patient taking other medications/products within 2 weeks of starting COVID-19 treatment. No treatment medications were reported.

Weitere VAERSDATA-Felder

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

VAERS 2290486

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: CT
Alter: 68,0
Geschlecht: F
Eingang: 23.05.2022
Impfdatum: 10.11.2021
Beginn: 07.05.2022
Tage bis Beginn: 178,0
Dosis: 3
Route/Site: SYR / AR

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

COVID-19 Fatigue Head discomfort Headache Oropharyngeal pain Pulmonary congestion Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

On the night of May 7th, 2022 I experienced symptoms. Significant sore throat and severe headache. There was a lot of upper respiratory congestion, and still a little left in my chest. The next day I tested for COVID and it was positive. I was seen on a telehealth appointment on that Tuesday, May 10th. I was prescribed Paxlovid. My symptoms started to get better around May 21st. I wasn't so fatigued and the head congestion eased up. I felt like I was finally turning the corner. I still have lingering symptoms, a little fatigue and congestion in the center of my chest.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: at home covid test- positive
Aktuelle Erkrankungen: None
Vorgeschichte: Lupus
Andere Medikamente: eye drops
Allergien: Amoxicillin, Gabapentin
Vorherige Impfungen: -

VAERS 2287383

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NJ
Alter: 43,0
Geschlecht: F
Eingang: 20.05.2022
Impfdatum: 17.11.2021
Beginn: 23.04.2022
Tage bis Beginn: 157,0
Dosis: 3
Route/Site: SYR / LA

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

Ageusia Anosmia Chills Diarrhoea Fatigue Laboratory test Nasal congestion Oropharyngeal pain Pain Pyrexia Viral test

Symptomtext

It started with a very bad sore throat, fatigue and nasal congestion. Chills, body aches, diarrhea, loss of taste and smell. I still don't have my taste or smell. My fever got up to 102.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: I took an at home test, I did a PCR test at a facility
Aktuelle Erkrankungen: NA
Vorgeschichte: Diabetes Type 2, Polycystic Ovarian Syndrome, Eczema
Andere Medikamente: Insulin, Metformin, Blood pressure medicine, Multivitamin, Vitamin B, Vitamin D, Jaurdince
Allergien: Seasonal allergies
Vorherige Impfungen: -

VAERS 2280733

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MI
Alter: 52,0
Geschlecht: F
Eingang: 17.05.2022
Impfdatum: 12.11.2021
Beginn: 21.04.2022
Tage bis Beginn: 160,0
Dosis: 3
Route/Site: SYR / LA

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

COVID-19 Chest discomfort Cough Headache Oropharyngeal pain Rhinorrhoea SARS-CoV-2 test positive Secretion discharge Sinus pain Upper respiratory tract infection

Symptomtext

I begin having upper respiratory infection cough, tightness in the chest, mucus, sore throat, sinus pain, runny nose, and a headache all within the course of a week. I did at-home COVID-19 test on 04/21/2022, and it came back positive. I called my doctor and prescribed cough syrup and informed me to rest. After 5-6 days of taking the syrup and quarantining, my symptoms began to go away and I recovered shortly after.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: COVID-19 test: 04/21/2022
Aktuelle Erkrankungen: N/A
Vorgeschichte: Fibromyalgia, IBFD, Graves' Disease
Andere Medikamente: Clonazepam, Cyclobenzaprine, Lexapro, Wellbutrin, Norco, Naproxen, Synthroid, Lyrica, Vitamin D3 supplement, Vitamin B-complex supplement
Allergien: N/A
Vorherige Impfungen: -

VAERS 2278266

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 13.05.2021
Beginn: 25.08.2021
Tage bis Beginn: 104,0
Dosis: 3
Route/Site: SYR / LA

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

Accident Concussion Disturbance in attention Dizziness Exercise tolerance decreased Fatigue Impaired work ability Insomnia Musculoskeletal stiffness Neck pain Pain Post concussion syndrome Visual impairment

Symptomtext

Concussion and subsequent post concussion syndrome. Occurred 8/25/21 treatment is ongoing with neurologist. Have received Physical and Occupational Therapy. Physical Therapy is ongoing. Have not returned to full physical activity (workouts) or a full work schedule since day of accident. Symptoms are throbbing, dizziness, neck pain and stiffness, fatigue, vision problems, and problems sleeping and concentrating. The vision problems and acute pain and dizziness are mostly resolved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: Chronic migraine, IBS with constipation, exercise induced asthma (seasonal), seasonal allergies
Andere Medikamente: Trokendi, Breo Ellipta, Linzess, Multivitamin, Vitamin C, Vitamin D, CoQ10, Calcium, Vitamin B, Biotin
Allergien: Antibiotics (most), latex (contact dermatitis), wheat, dairy
Vorherige Impfungen: -

VAERS 2271021

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CA
Alter: 75,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 05.11.2021
Beginn: 28.04.2022
Tage bis Beginn: 174,0
Dosis: 3
Route/Site: SYR / RA

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

COVID-19 Chills Nasopharyngitis Pyrexia SARS-CoV-2 test positive

Symptomtext

I had a high temperature of 103. I felt like I had a cold, chills, and they lasted 2 days. The day my symptoms started I received the IV infusion. My daughter is a nurse, so she was able to find me the infusion place.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 test: Positive
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroidism
Andere Medikamente: Synthroid Cholestyramine Multivitamin Calcium with Citrate with Magnesium and Zinc Cranberry Iron B12
Allergien: None
Vorherige Impfungen: -

VAERS 2270861

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 11.05.2022
Impfdatum: 23.03.2021
Beginn: 03.02.2022
Tage bis Beginn: 317,0
Dosis: UNK
Route/Site: - / -

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

Abdominal pain COVID-19 SARS-CoV-2 test positive

Symptomtext

02/03/22 presents to ED for "abdominal pain". PMHx of "recurrent pancreatitis, diverticulitis and intramular abscess (2020) and stable benign pancreatic IPMN"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: 02/03/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2268111

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: TX
Alter: 75,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 01.04.2022
Beginn: 09.04.2022
Tage bis Beginn: 8,0
Dosis: 4
Route/Site: SYR / LA

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

COVID-19 Chills Fatigue SARS-CoV-2 test positive Sinus operation Vaccine breakthrough infection

Symptomtext

COVID-19 breakthrough. Initially it was extreme fatigue. I never felt that tired before. Later I had the chills, they lasted just right before I fell a sleep. I also felt like I sinus drainage. The next day I felt much better.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: COVID-19 test- positive
Aktuelle Erkrankungen: None
Vorgeschichte: High cholesterol High blood pressure
Andere Medikamente: Multivitamin and minerals Losartan Neomycin polymyxin B sulfate Dexamethasone Ophthalmic ointment CoQ10 Vitamin D3 B complex B12 Lysine Turmeric extract Citracal Magnesium
Allergien: None
Vorherige Impfungen: -

VAERS 2267635

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: TX
Alter: 37,0
Geschlecht: F
Eingang: 09.05.2022
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Urticaria

Symptomtext

It started about 10 days after the vaccination, and it progressively got worse. It started near my eye and around my hairline and scalp. It progressively covered my entire body. I went to the doctor on Monday November 15, 2021, for the hives and he prescribed prednisone 10mg and Kenalog ointment. It helped with the issue and the doctor recommended an antihistamine. I take Xyzal but when I miss a dose, I do break out in hives again especially on my legs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Flu like symptoms from the previous vaccination that lasted for 2 days.
Vorgeschichte: None
Andere Medikamente: Ibuprofen
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2264704

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 78,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 03.11.2021
Beginn: 02.05.2022
Tage bis Beginn: 180,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Feeling abnormal Loss of personal independence in daily activities Oropharyngeal pain Pain Rhinorrhoea SARS-CoV-2 test positive Sneezing

Symptomtext

On the day that I had the 3rd dose of the vaccine, I was not able to function or go about my daily chores. I experienced aches, pains and exhaustion which lasted only 24 hours. I started having a sore throat recently with no fever. The 2nd day I had sneezing runny nose, aches, pains and tiredness. Today I developed a light cough. I used a home testing kit and I tested positive. I reached out to the doctor who recommended that I take Tylenol, rest and have fluids. As well as self isolating for 5 days. I woke up feeling miserable but a bit better now. I am still on the mend but not completely recovered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Osteoporosis
Andere Medikamente: Hydrochlorothiazide Multivitamin Calcium Zinc
Allergien: Fosamax
Vorherige Impfungen: -

VAERS 2264595

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 42,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 17.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Blood test Hypersensitivity Pruritus

Symptomtext

I started getting symptoms of itchiness on the tops and bottom of my feet. That continued to my legs and arms. It was extreme itching and I couldn't sit still. Nothing was visible on my skin. It was like the same reaction as I have to sulfa drugs. I have went to my doctor and was advised to go to an allergist which is scheduled for the future. I was prescribed a methylprednisolone steroid medication and I also take an Aller-Tec allergy pill everyday. This is still ongoing to this day that is always present.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Blood work.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Simvastatin, Fluoxetine, Synthroid, Oxybutynin
Allergien: Sulfa
Vorherige Impfungen: -

VAERS 2263332

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 44,0
Geschlecht: F
Eingang: 04.05.2022
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Pain in extremity

Symptomtext

Severe arm pain that has increased with time, treated with prednisone, awaiting EMG (5/23/22)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: EMG 5/23/22
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hashimoto's Disease Abnormal MRI - Liver High Blood Pressure Chronic back pain Erosive Esophagitis
Andere Medikamente: Levothyroxine Ibuprofen Gabapentin Lisinopril Omeprazole
Allergien: N/A
Vorherige Impfungen: -

VAERS 2260473

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: TX
Alter: 45,0
Geschlecht: F
Eingang: 02.05.2022
Impfdatum: 29.10.2021
Beginn: 18.04.2022
Tage bis Beginn: 171,0
Dosis: 3
Route/Site: IM / LA

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

Back pain COVID-19 Cough Oropharyngeal pain Pain Pyrexia SARS-CoV-2 test positive Taste disorder

Symptomtext

On April 11th 2022, I began with a mild sore throat and changes to my sense of taste. The next day, I had body aches and my sore throat was worsening. I then began to have a fever and continued to run a fever for 5 or 6 days. My sore throat developed into a dry cough after a few days. On day 11, I began experiencing back pain and on day 14, I woke up with a sore throat.

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Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: At home COVID-19 test.-April 19th-positive, At home COVID-19 test April 30th negative
Aktuelle Erkrankungen: None.
Vorgeschichte: TMJD, Headaches, Chronic back/neck pain
Andere Medikamente: Women's Multi-Vitamin, B12 Vitamin 2500MCG, D3 125 MCG, K2 100 MCG, Vegan Omega 3, Magnesium 400mg, Zyrtec as needed, Immuno-therapy drops for allergies, Clobetasol
Allergien: Imitrex
Vorherige Impfungen: Arm rash on two previous Covid vaccines.

VAERS 2260374

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 67,0
Geschlecht: M
Eingang: 02.05.2022
Impfdatum: 30.10.2021
Beginn: 26.12.2021
Tage bis Beginn: 57,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19 Cough Feeling abnormal Nasal congestion Pyrexia Respiratory tract congestion SARS-CoV-2 test positive

Symptomtext

Woke up that day and felt Nasally and had a slight cough. I started to feel bad, and had a slight fever of 100.3 just before bed. The next 4 days I had just slight congestion and a cough.

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Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: COVID-19 Positive test. 12/28/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: Type 2 Diabetes, Congestive Heart Failure, Glaucoma
Andere Medikamente: Entresto, IC Metoprolol, IC Metformin, IC Glipizide, IC Rosuvastatin Calcium, Aspirin, IC Dorzolamide-E-Timolol, Travoprost, Loteprednol Etabonate Ophthalmic, Monedine Titrate Arthometric Solution, Berbrine, Release, Goli Apple Cider Vineg
Allergien: N/A
Vorherige Impfungen: -

VAERS 2248045

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: MI
Alter: 30,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 31.03.2021
Beginn: 01.09.2021
Tage bis Beginn: 154,0
Dosis: 3
Route/Site: SYR / LA

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

Fibromyalgia Laboratory test

Symptomtext

I was diagnosed with fibromyalgia early in 2022. I don?t think the fibromyalgia syndrome is directly connected to the Covid-19 vaccines.

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Praegender Schweregrund: Fibromyalgia
Hospital-Tage: -
Labordaten: I had several tests done. I would need to contact doctors for info.
Aktuelle Erkrankungen: MDD, anxiety
Vorgeschichte: Fibromyalgia, asthma
Andere Medikamente: -
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2243651

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MD
Alter: 33,0
Geschlecht: M
Eingang: 20.04.2022
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Back pain Immunisation reaction Pain in extremity Posture abnormal Urticaria

Symptomtext

The next day I experienced pain in my arm and my back was hurting to the point I couldn't sit up straight up until about 1pm. I also experienced hive breakouts. I messaged my physician and she informed me it was and adverse but normal reaction. It lasted for about 48 hours. It was a 9 on Thursday and a 6 on Friday. I took naproxen over the first 24 hours of pain.

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Praegender Schweregrund: Back pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Cold
Vorgeschichte: Chronic migraines; Psoriasis; Irritable bowel syndrome; Chronic Allergies
Andere Medikamente: Candesartan; Lexapro; Claritin
Allergien: Gluten sensitivity; Lactose intolerance
Vorherige Impfungen: -

VAERS 2239100

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NH
Alter: 52,0
Geschlecht: F
Eingang: 18.04.2022
Impfdatum: 05.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Back pain Chills Fatigue Feeling cold Headache Injection site erythema Injection site pain Injection site pruritus Injection site swelling Injection site warmth Myalgia Pyrexia Upper-airway cough syndrome

Symptomtext

Vaccination received 3:15PM 11/05/21. At 5PM ? Onset of pronounced fatigue and mild soreness at injection site. 6PM ? Mild to moderate headache, muscle aches, low back pain, knee pain, and diffuse joint pain. 7PM to 10PM ? Onset of fever; very cold with chills; temp ranging from 99.5 -100.3 degrees F. 11/06/21 Sat. 8AM to 10PM - Headache, feeling cold/chilled and feverish, itching, swelling, pain, and redness at injection site. Post nasal drip, low back pain, knee pain, diffuse joint pain; muscle aches and joint pain moderate to severe. 11/07/21 Sun. 8AM-4PM Post nasal drip. Soreness at injection site - moderate. Postnasal drip. Low back pain, knee pain, diffuse joint pain; muscle aches and joint pain mild. 11/08/21 Mon. All symptoms resolved.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: No known illnesses
Vorgeschichte: Migraine headache
Andere Medikamente: Multivitamin and Mineral supplement Vitamin D3 5000 iu Zeaxanthin 2mg and Lutein 10 mg ProEFA 3-6-9 Fish Oil by Nordic Naturals Magnesium Citrate 650 mg
Allergien: Penicillin; Flagyl
Vorherige Impfungen: All three prior Moderna COVID-19 Vaccines; VAERS reports filed with description of adverse events (1/08/21, 2/05/21, and 11/05/2

VAERS 2220250

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: NJ
Alter: 82,0
Geschlecht: M
Eingang: 07.04.2022
Impfdatum: 10.12.2021
Beginn: 12.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Blood test Chest X-ray Dizziness Muscular weakness

Symptomtext

booster dizziness continued weakness in legs last 3 months to present day

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Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: chest x ray blood work
Aktuelle Erkrankungen: diabetis
Vorgeschichte: diabetis seizures
Andere Medikamente: metoprolol tartrate 25 mg, glipizide er10mg ,keppra 500mg clopidogrel 75mg
Allergien: -
Vorherige Impfungen: -

VAERS 2213973

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: OH
Alter: 64,0
Geschlecht: F
Eingang: 04.04.2022
Impfdatum: 18.11.2021
Beginn: 24.12.2021
Tage bis Beginn: 36,0
Dosis: 3
Route/Site: IM / LA

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

Acute sinusitis Cough Fatigue Headache Illness SARS-CoV-2 test negative Secretion discharge Sinusitis Sinusitis bacterial

Symptomtext

Illness occurred after the 3rd dose (booster) in November, 2021. Onset was mid-December, with symptoms of sinus infection, mild fatigue. Symptoms worsened over a week and I sought treatment beginning on December 31, 2021. Yellowish discharge from nose, uncontrollable cough, headache and mild fever (99-100). First treated with Augmentin 875 mg (2/day for 7 days), infection did not clear up. Sought treatment again January 14, 2022- diagnosis: acute bacterial sinusitis. Treatment was Doxycycline 100mg (2/day for 7 days and prednisone dosepak for 7 days. Infection did not clear up. Sought treatment again February 11, 2022. Diagnosis acute maxillary sinusitis. Treatment: Levaquin 500mg (1/day for 7 day). Infection finally cleared up and symptoms dwelt away.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 2 Covid-19 rapid tests at home. Both were negative.
Aktuelle Erkrankungen: Non
Vorgeschichte: Hypothyroid; colon polyp, postmenopausal
Andere Medikamente: Olly multi-vitamin, Zyrtec, Advil as needed, Advocare Probiotic
Allergien: Sulfa and latex
Vorherige Impfungen: Shingles vaccine, fever and body aches for 3 days, 62 y.o. Not sure of date or brand. Received vaccine at Pharmacy

VAERS 2206734

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: GA
Alter: 61,0
Geschlecht: F
Eingang: 30.03.2022
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

Arthralgia Arthritis Cluster headache Fatigue Influenza like illness Myalgia X-ray

Symptomtext

I had Flu like symptoms for 3 days. Then I was so tired, and my muscles and knees hurt all the time. Went to doctor about my legs hurting. The doctor says it's arthritis, and orthopedic doctor confirms it is probably arthritis. Typically after 3 pm, I need to nap. I am also experiencing headaches that are not normal.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Xrays
Aktuelle Erkrankungen: None
Vorgeschichte: Rheumatoid arthritis, Hypothyroidism, Lupus, FE, Acid reflux
Andere Medikamente: Levothyroxine, Losartan, Hydroxychloroquine, Vitamin E, Atorvastatin, Nexium, Singulair, Zyrtec, Osteo Bi-Flex with turmeric, Elderberry Zinc, Krill oil, Vitamin D, Tylenol, Ibuprofen
Allergien: Chickpeas, Latex, Some medical adhesives, Sulfa, Aspirin
Vorherige Impfungen: -

VAERS 2192163

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: GA
Alter: 70,0
Geschlecht: M
Eingang: 22.03.2022
Impfdatum: 10.11.2021
Beginn: 01.02.2022
Tage bis Beginn: 83,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia X-ray X-ray limb X-ray of pelvis and hip

Symptomtext

Persistent pain in right and left shoulders and pain in both hip joints and left knee

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: Xray of right shoulder March 3, 2022 X-ray of back and hips March 9, 2022
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes, Hypertension, IBS
Andere Medikamente: Celebrex 100 mg., Nexium 40 mg., Verapamil 180 mg., Simvastatin 40 mg., Allopurinol 100 mg., Glimepiride 4 mg., Allopurinol 100 mg., Breo Ellipta inhaler
Allergien: None
Vorherige Impfungen: -

VAERS 2189791

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 40,0
Geschlecht: M
Eingang: 21.03.2022
Impfdatum: 23.11.2021
Beginn: 08.12.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: SYR / LA

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

Eczema Pain in extremity Pruritus Rash Rash erythematous

Symptomtext

The patient had no immediate reactions to the second dose of the vaccine, except for arm soreness which resolved in 24 hours. One to two week later, the patient developed a global widespread swollen red patches all over the body. The whole body would itch aggressively including head scalp. The red patches will keep appearing at any random location. Clinic detected eczema like symptoms and recommended antihistamine cetirizine (ZyrTEC) , white petroleum mineral oil (vaseline) and steroid ointments (hydrocortisone). Patient applied for few days. The symptoms would go away and reappear next day. After few days its reappearing every two days. Patient is taking ZyrTEC and feels good for 2 days and have to take recurring medicine. Patient has no history of allergy, side effects or any health conditions. This has become chronic.

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Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: December 11, Atopic Dermatitis, unspecified type. cetirizine (ZyrTEC) , white petroleum mineral oil, hydrocortisone recommended
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 2170994

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 39,0
Geschlecht: M
Eingang: 10.03.2022
Impfdatum: 22.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: - / -

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

Dizziness Feeling hot Hyperhidrosis

Symptomtext

Moderna COVID-19 Vaccine Vaccine Lot Number: 033F21A FluLaval Quadrivalent Vaccine Lot Number: 579C9 client got flu shot and felt faint. had covid vaccine in medical tent on cot. has had syncopal episodes post vaccine and blood draw in past. stayed in medical tent for 40mins. drank 2 bottles of water. RN Felt faint after getting flu vaccine, but then given COVID vaccine (in tent). No hx of HTN, HT DZ or allergies or diabetes. given additional 2 (6 oz bottles of h20) and crackers. lungs were CTA no swelling, hives or n/v or abd pain. Anxiety, hot and sweaty, felt faint but did not faint. no problem breathing, swelling or hives or abdominal or chest pain. Pt wanted to drive self and wanted to return to work despite asking him to have wife drive him and take pm off from work. 12:10 110/79 p76 r16 97% sitting 12:20 112/74 p60 r16 96% lying 12:30 110/54 p55 r16 95% lying 12:30 111/73 p64 r16 97% standing 12:35 110/74 p66 r16 98% standing

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

VAERS 2167994

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: AZ
Alter: 69,0
Geschlecht: F
Eingang: 09.03.2022
Impfdatum: 04.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 27,0
Dosis: 3
Route/Site: SYR / LA

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

Burning sensation Corrective lens user Crying Discomfort Dry eye Eye complication associated with device Ophthalmological examination abnormal Pain

Symptomtext

Early Fall I had gotten new contact lenses and was comfortably wearing them 10-11 hrs per day; Dr. saw me for f/u and said that they fit well and were being tolerated well. In December I started to have burning when I put them in and had to wear them less time. I tried drops or took them out to rewet. By the end of December I had excruciating burning that made me cry from pain. I stopped wearing them until I could be seen for f/u on 1/5. I was told that my eyes were very dry and that I "can't wear contact lenses"; there was no explanation about the change in my condition. I was told that perhaps I could wear them 1-2 hrs on special occasions; I tried one more time and the burning was excruciating causing me to cry from discomfort. Only recently did I begin to question if this could be an adverse effect from the vaccine since no other professional could state anything except that I now have exceptionally dry eyes and need to use drops multiple times daily.

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Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Dr. checked my eyes on 1/5 to check on eye health and how the contact lenses were now fitting. This was when he made the assessment. All earlier appt visits had never had indications/discussions about dry eyes nor that contact lenses would not be tolerated.
Aktuelle Erkrankungen: -
Vorgeschichte: PCS (MVA), MVP, slightly elevated BP
Andere Medikamente: Baby aspirin, lisinopril 2.5, amoxicillin pre dental, vit D, Vit C, biotin, astaxanthin, lutein, calcium, magnesium, zinc, DGL (prn), B100, ibuprofen (prn), melatonin (prn), probiotic
Allergien: doxy, sulfa, seasonal allergies/pollen
Vorherige Impfungen: 02/21; 3/21 Moderna- age 68; chills/shaking and heat, insomnia, muscle aches and injection site pain/trouble lifting arm

VAERS 2155723

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NY
Alter: 48,0
Geschlecht: M
Eingang: 03.03.2022
Impfdatum: 03.11.2021
Beginn: 08.01.2022
Tage bis Beginn: 66,0
Dosis: 3
Route/Site: SYR / LA

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

Ear discomfort Ear pain Tinnitus

Symptomtext

One month after booster, sudden Fullness in ear and Tinnitus and discomfort to eardrums.

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Praegender Schweregrund: Ear pain
Hospital-Tage: -
Labordaten: ENT performed scope into both nostrils, visual inspection of both ears and throat exhibited no findings. Normal although effects were currently being felt.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Thyroid, blood pressure meds
Allergien: NONE
Vorherige Impfungen: -

VAERS 2137083

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 24.02.2022
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Fatigue Headache Nasal congestion Pain Pyrexia

Symptomtext

Day after vaccine - fever 100.5 to 101.8, fatigue, stuffy nose, headache, chills, body aches

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: Vaccine triggered the start of a oral herpes outbreak, but valtrex kept it from happening.
Vorgeschichte: Anemia
Andere Medikamente: Lysine, prenatal vitamin (not for pregnancy), iron supplement, probiotics, valtrex as needed.
Allergien: Penicillin, cefdinir, latex, diflucan
Vorherige Impfungen: -

VAERS 2131035

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: PA
Alter: 57,0
Geschlecht: F
Eingang: 22.02.2022
Impfdatum: 15.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: SYR / UN

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

Diarrhoea Herpes zoster Ophthalmic herpes zoster Rash Trigeminal nerve disorder

Symptomtext

I had shingles and with the shingles I had severe diarrhea. Shingles was in my scalp, around my forehead and eyes, and the trigeminal nerve was affected most strongly. I did not catch it in the first 72hrs so the prescription meds wasn't prescribed. I took homeopathic meds and had ointment for the rash.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: NO
Aktuelle Erkrankungen: NO
Vorgeschichte: I HAVE AN EYE DISEASE CALLED KERTATONUS
Andere Medikamente: CALCIUM, VITAMIN D3
Allergien: NOT THAT I KNOW OF
Vorherige Impfungen: -

VAERS 2123091

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 60,0
Geschlecht: M
Eingang: 18.02.2022
Impfdatum: 12.02.2022
Beginn: 13.02.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Blood pressure increased Hypoacusis Nausea Tinnitus Vertigo

Symptomtext

Vertigo with nausea Increase in blood pressure Partial hearing loss in right ear due to increased tinnitus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroidism, hypertension, COPD
Andere Medikamente: Losartan; Duloxetine, Levothyroxine, Buproprion, Rosuvastatin, Gabapentin, Tamsulosin, 81 mg Aspirin, Advil
Allergien: Tolectin Codeine
Vorherige Impfungen: Vertigo with vomiting, started 04/23/2021; 59; 04/14/2021; COVID; Moderna; 039B21A

VAERS 2114212

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NJ
Alter: 35,0
Geschlecht: M
Eingang: 15.02.2022
Impfdatum: 14.02.2021
Beginn: 18.11.2021
Tage bis Beginn: 277,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Mechanical urticaria Pruritus Rash macular Urticaria

Symptomtext

Booster was received on 11/04/2021. By 11/18/2021, extensive itching and redness on hands, feet, limbs, and torso was noted. Dermatographia / hives were also experienced. Primary care doctor provided me with Prednisone, as we thought this may have been a reaction to Omnicif that I was taking for a sinus infection around the same time as the booster. The Prednisone removed the extensive itching and redness, but it later returned. The overall itching and dermatographia has persisted to this day, but has been significantly reduced. I am able to control the symptoms by taking Allegra once every few days. I note the itching mainly at night around 7 PM. The dermatographia and hives occur randomly every few days and fade after 30 minutes. If I stop taking the Allerga, the symptoms will return to an uncomfortable level, including embarrassing red blotches and lines all over my face and body.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: None. I will be discussing with my primary care doctor to see if there are options for testing and treating this.
Aktuelle Erkrankungen: None. Sinus Infection prior to booster. Moderna booster was on 11/4/2021.
Vorgeschichte: -
Andere Medikamente: -
Allergien: Amoxicillin, MRI Contrast dye.
Vorherige Impfungen: -

VAERS 2109469

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21a

mild

Staat: PA
Alter: 45,0
Geschlecht: M
Eingang: 12.02.2022
Impfdatum: 03.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / RA

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

Albumin globulin ratio Allergy test positive Anxiety Basophil count Basophil percentage Blood albumin Blood alkaline phosphatase Blood bilirubin Blood chloride Blood cholesterol Blood creatinine Blood glucose normal Blood immunoglobulin E Blood potassium Blood test Blood thyroid stimulating hormone Blood triglycerides Blood urea

Symptomtext

Diagnosis 1: Urticaria, unspecified (L50.9) Allergic rhinitis, unspecified (J30.9) Other pruritus (L29.8) Patient has urticaria for the past 2 weeks - probably as a response to the Covid vaccine's immune boost. Hives are usually harmless but annoying. Several factors can be causing chronic hives including physical (heat, cold, rubbing, pressure, inflammation or infection) and psychological (stress, anxiety) factors. For now the most important task is to get the itch and therefore hives under better control. I recommend daily prophylactic medication with Zyrtec and Xyzal once or twice per day. For break-through episodes, benadryl 25mg every 4-6 hrs. Diagnosis 1: Chronic cough (R05.3) Allergic rhinitis, unspecified (J30.9) Procedures ordered or performed: Allergy Skin Tests (95004): Results: all positive - dermatographism, DX 1: R05.3, DX 2: J30.9, Venipuncture, Routine (36415): DX 1: J30.9. DX2: L50.9. DX3: R05.3. Patient has less cough, but still nasal congestion. Skin testing today was positive for all including negative control - due to his dermatographism. I sent an allergy blood test instead. In the meantime he should restart the combination of flonase and azelastine nasal sprays and continue the montelukast at night. For his skin itch he can use Zyrtec or Xyzal as needed. I will give him a call with his blood allergy test results and we can discuss avoidance measure and possibly consider allergy shots for more permanent treatment. Environmental controls discussed:

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: Bloodwork 11/16/21, Ordered Items: CBC With Differential/Platelet; Comp. Metabolic Panel (14); Lipid Panel; Hemoglobin A1c; TSH; Prostate-Specific Ag; Sex: Male Sedimentation Rate-Westergren; C-Reactive Protein, Quant Date Collected: 11/16/2021 Date Received: 11/17/2021 Date Reported: 11/17/2021 Fasting: No CBC With Differential/Platelet Test WBC 01 RBC 01 Hemoglobin 01 Hematocrit 01 MCV 01 MCH 01 MCHC 01 RDW 01 Platelets 01 Neutrophils 01 Lymphs 01 Monocytes 01 Eos01 Basos 01 Neutrophils (Absolute) 01 Lymphs (Absolute) 01 Monocytes(Absolute) 01 Eos (Absolute) 01 Baso (Absolute) 01 Immature Granulocytes 01 Immature Grans (Abs) 01 * Previous Reference Interval: (RDW: 12.3-15.4 % %) Comp. Metabolic Panel (14) Test Glucose 01 BUN 01 Creatinine 01 BUN/Creatinine Ratio Sodium 01 Potassium 01 Chloride 01 Carbon Dioxide, Total 01 Current Result and Flag Previous Result and Date 4.3 06/06/2019 6.21 06/06/2019 13.7 06/06/2019 43.2 06/06/2019 70 06/06/2019 22.1 06/06/2019 31.7 06/06/2019 16.2* 06/06/2019 208 06/06/2019 61 06/06/2019 28 06/06/2019 8 06/06/2019 2 06/06/2019 1 06/06/2019 2.6 06/06/2019 1.2 06/06/2019 0.4 06/06/2019 0.1 06/06/2019 0.0 06/06/2019 0 06/06/2019 0.0 06/06/2019 Previous Result and Date 80 06/06/2019 16 06/06/2019 1.17 06/06/2019 76 06/06/2019 88 06/06/2019 Units x10E3/uL x10E6/uL g/dL % fL pg g/dL % x10E3/uL % % % % % x10E3/uL x10E3/uL x10E3/uL x10E3/uL x10E3/uL % x10E3/uL Units mg/dL mg/dL mg/dL mL/min/1.73 mL/min/1.73 Reference Interval 3.4-10.8 4.14-5.80 13.0-17.7 37.5-51.0 79-97 26.6-33.0 31.5-35.7 11.6-15.4 150-450 Not Estab. Not Estab. Not Estab. Not Estab. Not Estab. 1.4-7.0 0.7-3.1 0.1-0.9 0.0-0.4 0.0-0.2 Not Estab. 0.0-0.1 Reference Interval 65-99 6-24 0.76-1.27 >59 >59 9-20 134-144 3.5-5.2 96-106 20-29 Final Report Page 1 of 3 7.8 6.62 High 14.5 45.7 69 Low 21.9 Low 31.7 17.0 High 203 77 14 8 0 0 6.1 1.1 0.6 0.0 0.0 1 0.1 Current Result and Flag 115 High 17 1.01 89 103 17 136 3.6 99 24 14 06/06/2019 143 06/06/2019 4.7 06/06/2019 101 06/06/2019 18 06/06/2019 mmol/L mmol/L mmol/L mmol/L Date Created and Stored 11/17/21 0807 ET This document contains private and confidential health information. 9.8 06/06/2019 7.3 06/06/2019 4.9* 06/06/2019 2.4 06/06/2019 2.0 06/06/2019 0.3 06/06/2019 47* 06/06/2019 Specimen ID: 320-339-5738-0 Comp. Metabolic Panel (14) (Cont.) Calcium 01 Protein, Total 01 Albumin 01 Globulin, Total A/G Ratio Bilirubin, Total 01 Alkaline Phosphatase 01 AST (SGOT) 01 ALT (SGPT) 01 * Previous Reference Intervals: (Albumin: 3.5-5.5 g/dL g/dL), (Alkaline Phosphatase: 39-117 IU/L IU/L) Sex: Male 9.7 7.1 4.7 2.4 2.0 0.4 52 mg/dL 8.7-10.2 g/dL g/dL g/dL mg/dL IU/L 6.0-8.5 4.0-5.0 1.5-4.5 1.2-2.2 0.0-1.2 44-121 0-40 0-44 Reference Interval 100-199 0-149 >39 5-40 0-99 Reference Interval 4.8-5.6 Reference Interval 0.450-4.500 Reference Interval 0.0-4.0 **Please note reference interval change** 22 31 24 06/06/2019 IU/L IU/L Units mg/dL mg/dL mg/dL mg/dL mg/dL Units % Units uIU/mL Units ng/mL 27 06/06/2019 Lipid Panel Test Cholesterol, Total 01 Triglycerides 01 HDL Cholesterol 01 VLDL Cholesterol Cal LDL Chol Calc (NIH) Hemoglobin A1c Test Hemoglobin A1c 01 Please Note: 01 TSH Test TSH 01 Prostate-Specific Ag Test Prostate Specific Ag 01 Current Result and Flag Current Result and Flag Previous Result and Date 218 06/06/2019 62 06/06/2019 57 06/06/2019 Previous Result and Date 6.4 06/06/2019 226 High 58 65 10 151 High 6.3 High Prediabetes: 5.7 - 6.4 Diabetes: >6.4 Glycemic control for adults with diabetes: <7.0 Current Result and Flag 0.455 Current Result and Flag 1.1 Previous Result and Date 0.7 06/06/2019 Previous Result and Date 1.2 06/06/2019 Serum PSA should decrease and remain at undetectable levels after radical prostatectomy. The AUA defines biochemical recurrence as an initial PSA value 0.2 ng/mL or greater followed by a subsequent confirmatory PSA value 0.2 ng/mL or greater. Values obtained with different assay methods or kits cannot be used interchangeably. Results cannot be interpreted as absolute evidence of the presence or absence of malignant disease. Date Created and Stored 11/17/21 0807 ET Final Report Page 2 of 3 Previous Result and Date Previous Result and Date Sedimentation Rate-Westergren Test Sedimentation Rate-Westergren 01 C-Reactive Protein, Quant Test C-Reactive Protein, Quant 01 22 High Disclaimer Sex: Male Current Result and Flag 23 High Units mm/hr Units mg/L Reference Interval 0-15 Reference Interval 0-10 Current Result and Flag The Previous Result is listed for the most recent test in the past 3 years where there is sufficient patient demographic data to match the result to the patient. Icon Legend Out of reference range Critical or Alert Performing Labs 01: RN - Patient Details Date Collected: 11/16/2021 1016 Local Date Received: 11/17/2021 0000 ET Date Entered: 11/17/2021 0139 ET Date Reported: 11/17/2021 This document contains private and confidential health information. Date Created and Stored 11/17/21 0807 ET Final Report Page 3 of 3 My account | Sign out Gender: Male Sending Facility: RN Date Entered: 01/25/2022 00:00 Date Collected: 01/25/2022 12:50 Date Reported: 01/30/2022 16:05 Home Patient Messages Health Information Test Name In Range Out Of Range Units Ref Range Status Site ID Allergens w/Total IgE Area 1 - 01/25/2022 12:50 - Result Status: Final Class Description - - - Final BN Levels of Specific IgE Class Description of Class --------------------------- ----- -------------------- < 0.10 0 Negative 0.10 - 0.31 0/I Equivocal/Low 0.32 - 0.55 I Low 0.56 - 1.40 II Moderate 1.41 - 3.90 III High 3.91 - 19.00 IV Very High 19.01 - 100.00 V Very High >100.00 VI Very High Immunoglobulin E, Total 23 - IU/mL 6-495 Final BN D001-IgE D pteronyssinus <0.10 - kU/L Class 0 Final BN D002-IgE D farinae <0.10 - kU/L Class 0 Final BN E001-IgE Cat Dander <0.10 - kU/L Class 0 Final BN E005-IgE Dog Dander <0.10 - kU/L Class 0 Final BN G002-IgE Bermuda Grass <0.10 - kU/L Class 0 Final BN G006-IgE Timothy Grass <0.10 - kU/L Class 0 Final BN I006-IgE Cockroach, German <0.10 - kU/L Class 0 Final BN M001-IgE Penicillium chrysogen <0.10 - kU/L Class 0 Final BN M002-IgE Cladosporium herbarum <0.10 - kU/L Class 0 Final BN M003-IgE Aspergillus fumigatus <0.10 - kU/L Class 0 Final BN M006-IgE Alternaria alternata <0.10 - kU/L Class 0 Final BN T001-IgE Maple/Box Elder <0.10 - kU/L Class 0 Final BN
Aktuelle Erkrankungen: -
Vorgeschichte: Hypertension Asthma
Andere Medikamente: 1. TRIAMTERENE-HCTZ 37.5-25 MG TB TABLET 2. AMLODIPINE BESYLATE 5 MG TAB TABLET 3. MONTELUKAST SOD 10 MG TABLET 4. AZELASTINE 0.1% (137 MCG) SPRAY 5. FLUTICASONE PROP 50 MCG SPRAY spray, suspension 6. ALBUTEROL HFA (PROAIR) INHALER HFA AERO
Allergien: -
Vorherige Impfungen: -

VAERS 2091890

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CA
Alter: 42,0
Geschlecht: M
Eingang: 06.02.2022
Impfdatum: 29.10.2021
Beginn: 19.11.2021
Tage bis Beginn: 21,0
Dosis: 1
Route/Site: - / LA

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

Fatigue Haemorrhoids Headache Impaired work ability Pain Pain in extremity Spinal pain

Symptomtext

Several days of fatigue and headache, pain in left arm right after vaccine. Then few weeks later, I started having severe pain at the base of my spine near the rectum which ended up being diagnosed as hemorrhoid's. I have never had this problem, and I have been healthy for many years. It took about 2-3 weeks to fully subside during which time it was very hard to work due to the pain.

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Healthy for past 2 years
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Allergic to penicillin, meat products
Vorherige Impfungen: When I was young and had regular vaccines - I often had allergic type reactions.

VAERS 2079847

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 36,0
Geschlecht: M
Eingang: 01.02.2022
Impfdatum: 03.12.2020
Beginn: 15.12.2020
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: SYR / RA

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

Blood test Influenza A virus test positive Influenza B virus test Peripheral swelling Pruritus SARS-CoV-2 test Urticaria

Symptomtext

On the evening of the 3rd vax, 12/15/2020 started feeling itchy on left wrist, then the next morning his hand was swollen to 3 times the size it normally is and had hives all over body. Went to Urgent Care where they gave blood tests for covid, and, influenza A and B. Tested positive for Influenza A. Did have the Flu vax in 8/2020, and didn't have any reaction. Never had a reaction to it. After he got the Booster Moderna vax is when he tested positive for Influenza A.

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Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Prescribed Tamiflu and a steroid.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Fish Oil, Multi-vitamin
Allergien: None
Vorherige Impfungen: -

VAERS 2071191

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: IN
Alter: -
Geschlecht: F
Eingang: 28.01.2022
Impfdatum: 10.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / LA

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

Rash Rhinorrhoea

Symptomtext

lot of mucus after the Moderna Covid-19 vaccine; developed a rash after her booster dose,The rash is on her back,neck, and part of her head.rash after the moderna Booster dose is not as severe as the rash was after the Johnson and Johnson vaccine.; This spontaneous case was reported by a consumer and describes the occurrence of RHINORRHOEA (lot of mucus after the Moderna Covid-19 vaccine) and RASH (developed a rash after her booster dose,The rash is on her back,neck, and part of her head.rash after the moderna Booster dose is not as severe as the rash was after the Johnson and Johnson vaccine.) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Johnson vaccine (The patient developed a severe blood clot in her eye and a severe rash on her neck. Rash went down her arms to her elbow and the rash lasted for several months.) in March 2021 and Johnson vaccine (The patient developed a severe blood clot in her eye and a severe rash on her neck. Rash went down her arms to her elbow and the rash lasted for several months.) in March 2021. Past adverse reactions to the above products included Clot blood with Johnson vaccine; and Rash with Johnson vaccine. On 10-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced RHINORRHOEA (lot of mucus after the Moderna Covid-19 vaccine) and RASH (developed a rash after her booster dose,The rash is on her back,neck, and part of her head.rash after the moderna Booster dose is not as severe as the rash was after the Johnson and Johnson vaccine.). The patient was treated with CORTISONE at an unspecified dose and frequency and CLOBETASOL PROPIONATE (CLOBETASOL 0.05%) at an unspecified dose and frequency. At the time of the report, RHINORRHOEA (lot of mucus after the Moderna Covid-19 vaccine) and RASH (developed a rash after her booster dose,The rash is on her back,neck, and part of her head.rash after the moderna Booster dose is not as severe as the rash was after the Johnson and Johnson vaccine.) outcome was unknown. No Concomitant medication was reported. treatment medication liquids, ointments, antihistamine. Patient says that she is in her sixties. The patient went to a Dermatologist and started to get better. Sleeping was difficult.

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

VAERS 2062926

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NH
Alter: 26,0
Geschlecht: F
Eingang: 25.01.2022
Impfdatum: 23.11.2021
Beginn: 04.12.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / RA

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

Chronic spontaneous urticaria Mechanical urticaria

Symptomtext

Chronic Spontaneous Uticaria, Demographia

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Praegender Schweregrund: Chronic spontaneous urticaria
Hospital-Tage: -
Labordaten: Seen at urgent care 12/5/21. Seen by PCP 12/20/21
Aktuelle Erkrankungen: Anxiety
Vorgeschichte: -
Andere Medikamente: Buspar, Kyleena
Allergien: Vigamox
Vorherige Impfungen: -

VAERS 2058819

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 70,0
Geschlecht: F
Eingang: 24.01.2022
Impfdatum: 29.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 2,0
Dosis: N/A
Route/Site: IM / LA

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

Disturbance in attention Headache Myalgia Pyrexia

Symptomtext

Day of booster vaccination had headache all night long. Following day had muscle aches in neck, shoulder, back, chills, low grade fever. On the third day, woke up feeling fine. Around 11:00 am, started to lose concentration and ability to complete a sentence. It got worse to the point where I couldn't even state a question. My friend was with me and did not notice anything else like paralysis to indicate a stroke, but brought me home to phone my doctor and pharmacist. Symptoms lasted for close to 1 hour and 30 minutes, and then everything returned to normal speech and thought processes. Both doctor and pharmacist said they both have seen three or four patients who reported the same thing happened to them.

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Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension, cholesterol
Andere Medikamente: Prozac, HCTZ, Losartan, Allegra
Allergien: Darvon, statin drugs , sulfa drugs, zetia, versed
Vorherige Impfungen: -

VAERS 2054213

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: OK
Alter: 61,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 19.11.2021
Beginn: 13.01.2022
Tage bis Beginn: 55,0
Dosis: 3
Route/Site: IM / LA

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

Ageusia Anosmia COVID-19 Cough Ear discomfort Fatigue Pyrexia Respiratory tract congestion Rhinorrhoea SARS-CoV-2 test positive Throat irritation

Symptomtext

FEVER, COUGH, LOSS OF TASTE/SMELL, RN/CONGESTION, FATIGUE, SCRATCHY THROAT, EAR PRESSURE

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: POSITIVE SARS-COV-2 RNA
Aktuelle Erkrankungen: NONE
Vorgeschichte: HTN, DM2, HYPERLIPIDEMIA
Andere Medikamente: LOSARTAN, CHOLECALCIFEROL, MUPIROCIN OINT, METFORMIN, ATORVASTATIN, MONTELUKAST, ASPIRIN
Allergien: NKA
Vorherige Impfungen: -

VAERS 2050600

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: PA
Alter: 72,0
Geschlecht: F
Eingang: 20.01.2022
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: ja

Injection site erythema Injection site warmth

Symptomtext

Antibiotic (Doxycycline) prescribed for infection after vaccination. Red spot at injection site, 3-4 inches, warm, not raised.

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

VAERS 2043127

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MI
Alter: 57,0
Geschlecht: M
Eingang: 18.01.2022
Impfdatum: 19.02.2021
Beginn: 16.01.2022
Tage bis Beginn: 331,0
Dosis: 3
Route/Site: - / -

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

Cough Pyrexia Respiratory tract congestion

Symptomtext

Pt has cerebral palsy and spastic quadriplegia. He has had worse congestion, cough, and a fever.

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

VAERS 2032413

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 64,0
Geschlecht: F
Eingang: 13.01.2022
Impfdatum: 23.12.2021
Beginn: 04.01.2022
Tage bis Beginn: 12,0
Dosis: 3
Route/Site: SYR / LA

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

Burning sensation Chills Decreased appetite Diarrhoea Erythema Flatulence Gastrooesophageal reflux disease Influenza like illness Nausea Pruritus Urticaria

Symptomtext

Chills and flu-like symptoms first 24 hours, then a few days later digestive symptoms (a lot of air, gas pain, some diarrhea). I had these same symptoms after the second vaccine very bad and they lasted about six weeks - worse in first three weeks then gradual improvement. This time the digestive symptoms weren't quite as intense but still bothersome. Then at about day 11 or 12 - I started to get a very itchy body all over. My groin area itched terribly and when I scratched it it became very red and huge hives developed. Then my back started to feel like it was on fire. Then my scalp. Then my wrists. I felt like my whole body had been bitten by fire ants. I could not keep myself from scratching and as I scratched I got worse and almost felt nauseous. I contacted my doctor who said this delayed reaction of hives was a common occurrence after the Moderna booster and to take some Zyrtec, Benadryl and Pepsid. The Zyrtec has helped to keep the itching to a bearable level but nothing has improved. If I stop the medicines the hives come back in full force and are unbearable. The medicine doesn't last very long before I need to take another. It has really stopped me from being able to do anything for the last few weeks. It's a very difficult situation that I wish there would be an answer for or at least some help to those of us who have it. I belong to a social media group of over two thousand people who have the exact same reaction to the Moderna booster. There are pictures on that page which are identical to the hives that I am experiencing and I also have photos. There is also a lot of information about this on the website pages. I also still have awful digestive symptoms - I feel like what is happening with the hives on my skin is the same thing that is happening inside my digestive tract. The Pepcid has helped some.

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Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: I haven't had any tests. Doctor just prescribed antihistamines.
Aktuelle Erkrankungen: I take pain medication for problems with adhesions in abdomen from previous hysterectomy but no other illnesses
Vorgeschichte: I take pain medication for problems with adhesions in abdomen from previous hysterectomy but no other illnesses
Andere Medikamente: Hydrocodone with acetaminophen the day before; possibly one 5mg Ativan two days before
Allergien: sensitive to MSG and Macrobid
Vorherige Impfungen: Moderna first and second vaccines I had a much less intense skin reaction; first one I had about seven or so skin eruptions that

VAERS 2028664

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MO
Alter: 47,0
Geschlecht: F
Eingang: 12.01.2022
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Bronchitis Cough Fatigue Lymphadenopathy Myalgia Nasopharyngitis Peripheral swelling Pyrexia Rhinorrhoea SARS-CoV-2 test negative Sinusitis

Symptomtext

11/8/21 - Booster shot - low grade fever, joint & muscle pain, swollen left arm, swollen left armpit, & fatigue. 11/22/21 - runny nose & coughing then sick with head cold symptoms with severe head congestion & coughing from 11/23/21 through 11/27/21. 11/29/21 - Negative COVID-19 Test 12/10/21 - telehealth doctors visit for sinus infection symptoms & bronchitis symptoms. Given Doxycycline (antibiotic), Predisone (steroid), and Albuterol Inhaler 3/1/21 2nd shot - severe headache, severe injection site arm pain into neck and shoulder. Pain in arm and shoulder lasted for 1 week after 2nd COVID shot on 3.1.21.

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Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None for booster shot given on 11/8/21
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Aspirin, Ibuprofen, & Tylenol
Allergien: Sulfa medications
Vorherige Impfungen: 2nd Moderna COVID-19 shot on 3/1/21 with 102 F fever, severe joint & muscle pain, severe fatigue & headac

VAERS 2028168

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: PA
Alter: 51,0
Geschlecht: M
Eingang: 12.01.2022
Impfdatum: 12.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

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

Borrelia test negative Carbon dioxide increased Erythema Fatigue Full blood count normal Metabolic function test Pruritus Rash Rash macular Sensitive skin Urticaria

Symptomtext

No immediate reaction aside from minor fatigue on 11/13. Awoke on 11/25 with hives-like bumps at waistline and right armpit. This progressed over the next week to 60-70% of body, including legs, almost entire torso, arms, face (forehead and cheeks), back of neck, hairline. Saw PCP on 11/26 who prescribed prednisone & benadryl. Helped affected areas but continued to spread to other areas. Saw PCP on 11/29. Rash was very atypical but some potential Lyme-type patterns on back of knee. Prescribed doxycycline on suspicion & hydroxyzine. Lyme test negative, but finished 14-day doxycycline course and ramped down prednisone. Acute reaction with active hive-like bumps went away by 12/6. However, high sensitivity of skin has persisted. Highly itchy, and when I itch, skin turns bright red and leaves raised lines in skin. I have red blotches that come and go on forehead (these have subsided). I also have regular acute itching 'attacks' about every 3 days, typically in the evening where I am super itchy. I have taken hydroxyzine to help with these symptoms and get to sleep. Symptoms have resolved by the next morning in each case. I also avoid wearing certain fabrics (e.g., flannel-type material is an irritant)

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Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Lyme progress 11/29 negative; had pending orders for physical so also took on 11/29 - comp metabolic was normal except Carbon Dioxide high at 31 mmol/L, CBC normal
Aktuelle Erkrankungen: None
Vorgeschichte: Inflammatory arthritis (no flareups since 2016), gastric MALT (remission since 2016)
Andere Medikamente: Omeprazole 40mg, Pepcid 20mg (reflux), plaquenil 200 (arth)
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2020873

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 83,0
Geschlecht: F
Eingang: 10.01.2022
Impfdatum: 16.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 6,0
Dosis: UNK
Route/Site: SYR / RA

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

Pruritus Rash

Symptomtext

Bad rash all over body . Very itchy been almost 5 weeks now . Took topicals did not work. Doctor prescribed prednisone. Cleared up alittle need to do another refill of prednisone in hopes it will clear up.

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Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Cardiomyopathy
Andere Medikamente: High blood pressure medication
Allergien: No
Vorherige Impfungen: -

VAERS 2019867

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: TX
Alter: 52,0
Geschlecht: F
Eingang: 09.01.2022
Impfdatum: 17.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / LA

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

Laboratory test normal Pruritus Rash Urticaria

Symptomtext

11/27/2021 I developed itching on my hands around 9:30pm. Itching became severe around 12:30am. I took Benadryl and all seemed okay until the next evening November 28, 2021 around 5:30pm. I developed hives on neck, behind ears, and on upper back. I took more Benadryl, which helped the itching and calmed the hives a bit, but rash did not go away. I woke up around 12:30am with severe itching and by 2:00am I decided to go to the ER as the hives were increasing and spreading over my body and the itching was increasing as well. The ER treated me and sent me home with prescriptions for anti-histamines and prednisone. I went to an allergist and my primary Care Dr.. They both stated I have Urticaria. Both Doctors stated that if the Urticaria continued for 6 weeks, it would be considered chronic. I have now had rashes/hives everyday for six weeks. I am currently taking Pepcid 2x/day, Allegra in the morning and afternoon, Singular in the morning, and Zyrtec at night. In addition, there are days where I need to take Benadryl as well.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Primary doctor tested for Sjogren's and Auto-immune Thyroid disease. Both Tests came back negative. Tests preformed on Dec. 21, 2021.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Estrogen, Progesterone, Multivitamin, collagen, glucosamine chondroitin.
Allergien: Besifloxacin and Macrobid
Vorherige Impfungen: -

VAERS 2019795

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NY
Alter: 51,0
Geschlecht: F
Eingang: 09.01.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Pruritus Rash macular

Symptomtext

Whole arm is blotchy and itchy

Weitere VAERSDATA-Felder

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

VAERS 2019653

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 68,0
Geschlecht: F
Eingang: 09.01.2022
Impfdatum: 15.11.2021
Beginn: 15.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain

Symptomtext

Sharp pain in arm at injection site every day since received booster with specific movements

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Multi vitamin?centrum
Allergien: Sulfa drugs
Vorherige Impfungen: -

VAERS 2019524

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: WI
Alter: 30,0
Geschlecht: F
Eingang: 08.01.2022
Impfdatum: 11.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / RA

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

Abortion spontaneous Exposure during pregnancy Human chorionic gonadotropin abnormal Loss of personal independence in daily activities Mechanical urticaria Pruritus Urticaria

Symptomtext

Dermatographia ongoing since 11/22/21 to now- chronic hives, itching, requiring medication to perform daily activities, Pregnancy ended in miscarriage at 6 weeks 4 days and as of now I am telling everyone I know, especially women, to NOT get the moderna vaccine at any time. Moderna better pray I can hold another successful pregnancy (I has 1 child before any vaccination from COVID).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: Hcg level 7000 on 1/1/22, hcg level 171 on 1/6/22 indicating miscarriage,
Aktuelle Erkrankungen: Anxiety
Vorgeschichte: N/A
Andere Medikamente: 5 mg Lexapro
Allergien: Fish allergy
Vorherige Impfungen: -

VAERS 2018781

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: IL
Alter: 34,0
Geschlecht: M
Eingang: 08.01.2022
Impfdatum: 20.11.2021
Beginn: 03.12.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Full blood count normal Metabolic function test Pruritus Scratch Skin swelling Urticaria

Symptomtext

2 weeks after receiving the booster shot, itching on hands and feet started moved into the rest of the body including trunk, neck, back. Get's worse when being scratched. Raised hives and red marks appear. Get's better after taking antihistamine, but continues to come and go throughout the day on a daily basis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: CBC and CMP were completed on 1/4/2022 and were within normal limits
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: N/A
Vorherige Impfungen: -

VAERS 2006427

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: FL
Alter: 34,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 02.01.2022
Beginn: 03.01.2022
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Lymph node pain Lymphadenopathy Pain Polymenorrhoea Pyrexia

Symptomtext

Around 20 hours after the booster shot was administered, I began menstruating. This was 9 days earlier than my very consistent, normal cycle. It has been complete menstruation of the same flow and duration of my usual period. This is also accompanied by very swollen, painful lymph nodes in my left armpit and the left side of my neck (side of the injection site). I also had a fever of 101.5 onsets 12 hours after injection lasting for 12 hours and severe body aches, but these were also present after the second dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lymph node pain
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Oral Contraception
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 2005441

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21A

mild

Staat: OH
Alter: 82,0
Geschlecht: F
Eingang: 05.01.2022
Impfdatum: 09.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Fatigue Pain in extremity Tinnitus

Symptomtext

Patient experiencing pain in knees and feet that comes and goes in the night time when she is sleeping.. Almost two months after vaccination patient reports tiredness and ringing in ears that has not resolved. Patient had a well visit on 11-30-2021 with primary care physician who stated she does not know if it was related to the vaccination.

Weitere VAERSDATA-Felder

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

VAERS 2001672

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: FL
Alter: 43,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Headache Rash Vertigo

Symptomtext

I experienced severe Vertigo, rashes on my leg, dizziness and headaches.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Hyperthyroidism
Andere Medikamente: Tapazole
Allergien: -
Vorherige Impfungen: -

VAERS 2001167

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 32,0
Geschlecht: F
Eingang: 04.01.2022
Impfdatum: 03.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / LA

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

Mechanical urticaria Pruritus Urticaria White blood cell count increased

Symptomtext

Developed hives and itching which needed IV steroids to help (has done away), also developed dermatagraphia which has not resolved yet (Jan 4 2022)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: Blood draw (Dec 16 2021) - normal other than high WBC but doctor said was due to oral steroids I took prior to IV steroids
Aktuelle Erkrankungen: None
Vorgeschichte: Thalessemia minor
Andere Medikamente: -
Allergien: Amoxicillin (as a baby)
Vorherige Impfungen: -

VAERS 1999341

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 46,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 23.12.2021
Beginn: 30.12.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / RA

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

Injection site discharge Injection site erythema Injection site pain Injection site swelling

Symptomtext

INITIAL REPORT OF REDNESS, SORENESS AT INJECTION SITE - APPROXIMATELY 7 DAYS AFTER VACCINATION REDNESS WORSENED AND 10 DAYS POST-VACCINATION AFTER ICE THEN HOT BATH THE SWOLLEN AREA BEGAN TO DRAIN A YELLOW/GREEN DISCHARGE . APPOINTMENT SCHEDULED FOR 1/4 WITH PCP FOR EVALUATION OF POTENTIAL INFECTION

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site discharge
Hospital-Tage: -
Labordaten: 1/4/22 - APPOINTMENT SCHEDULED WITH PRIMARY CARE TO ASSESS THE REACTION.
Aktuelle Erkrankungen: NONE REPORTED
Vorgeschichte: ASTHMA; MENTAL HEALTH
Andere Medikamente: MULTIVITAMIN; PROZAC; PRAZOSIN; OLANZAPINE; TRAZODONE; LORAZEPAM; AMLODIPINE
Allergien: NO KNOWN ALLERGIES
Vorherige Impfungen: -

VAERS 1998433

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: SC
Alter: 69,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 30.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: OT / -

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

Bowel movement irregularity Headache Myalgia Pyrexia Sleep disorder

Symptomtext

No bowel movement; Was awake every hour/Couldn't go back to sleep/ Was awake every 30 minutes; Headache; Fever; Body aches; This spontaneous case was reported by a consumer and describes the occurrence of SLEEP DISORDER (Was awake every hour/Couldn't go back to sleep/ Was awake every 30 minutes), BOWEL MOVEMENT IRREGULARITY (No bowel movement), HEADACHE (Headache), PYREXIA (Fever) and MYALGIA (Body aches) in a 69-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 069H21A and 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 30-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 28-Dec-2021, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In December 2021, the patient experienced HEADACHE (Headache), PYREXIA (Fever) and MYALGIA (Body aches). On 28-Dec-2021, the patient experienced SLEEP DISORDER (Was awake every hour/Couldn't go back to sleep/ Was awake every 30 minutes). On 29-Dec-2021, the patient experienced BOWEL MOVEMENT IRREGULARITY (No bowel movement). At the time of the report, SLEEP DISORDER (Was awake every hour/Couldn't go back to sleep/ Was awake every 30 minutes), BOWEL MOVEMENT IRREGULARITY (No bowel movement), HEADACHE (Headache), PYREXIA (Fever) and MYALGIA (Body aches) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided Patient hasn't tried any medication to alleviate the symptoms.

Weitere VAERSDATA-Felder

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

VAERS 1997933

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MD
Alter: 32,0
Geschlecht: F
Eingang: 02.01.2022
Impfdatum: 03.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / LA

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

Blood test normal Flushing Helicobacter test negative Laboratory test abnormal Platelet count decreased Swelling face Urticaria Vitamin D decreased White blood cell count decreased

Symptomtext

Flushing, hives, and facial swelling starting about 7-10 days after injection that lasted 6+ weeks. Triggers include touch, pressure, heat, and stress. PCP appointment 11/15/21 with recommendations of oral Benedryl, topical cortisone cream, and unscented laundry detergent. Consult with allergist 12/9/21 for persistent symptoms. Unable to complete skin testing 2/2 too reactive. Prescribed Allegra 2-3x/day and Famotidine 1x/day, as well as further reduction of environmental allergies, including avoiding high histamine foods.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: Blood work 12/16/21 (WNL except): - low WBC (2.9) | range 3.4-10.8 - low platelets (149) | range 150-450 - high cu index ( > 50) | range < 10 - low vitamin D (23.8) | range 30-100 - negative h pylori breath test
Aktuelle Erkrankungen: N/A
Vorgeschichte: - Easy bruising - Rare heart palpitations - Mild anxiety
Andere Medikamente: - Mirena IUD - Vitamin C & B12 - Probiotic
Allergien: N/A
Vorherige Impfungen: -

VAERS 1995794

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 42,0
Geschlecht: F
Eingang: 31.12.2021
Impfdatum: 26.11.2021
Beginn: 05.12.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: - / LA

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

Allergy test Chronic spontaneous urticaria Laboratory test Mechanical urticaria Rash Urticaria

Symptomtext

Chronic spontaneous Urticaria. Dermatographia urticaria. Symptoms started 12/6/2021. Rashes all over body. Hives all over body. ?Scratch rashes? all over body. These come and go all day. The symptoms have occurred every day since 12/6 onset.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chronic spontaneous urticaria
Hospital-Tage: -
Labordaten: Immunologist is running full panels of auto immune diseases & allergy tests. Results pending
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lamictal, Wellbutrin, Klonopin, fish oil, cranberry, vitamin D3
Allergien: None
Vorherige Impfungen: -

VAERS 1989285

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 60,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 17.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / AR

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

Urticaria Vaccination complication

Symptomtext

5 days after receiving the booster, I have since developed hives that randomly appear on my body, primarily the palms of my hands, feet soles, and upper trunk, arms, neck and head areas.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: Have met with allergy specialist who also suspects that I am having a reaction to the third dosage. He has prescribed Zyrtec, 1 pill, two times a day.
Aktuelle Erkrankungen: None
Vorgeschichte: Pacemaker, elevated blood pressure and triglycerides.
Andere Medikamente: Fenofibrate (Tricor) 145 mg, Ramipril (hbp) 5 mg, 2 baby aspirin, Fish oil, Multivitamin, Lorazepam .5 mg
Allergien: None
Vorherige Impfungen: -

VAERS 1988845

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 61,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 01.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: IM / LA

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

Abnormal dreams Anxiety Fatigue Poor quality sleep

Symptomtext

Since getting this booster I have felt chronically tired. My sleep quality has been poor with vivid dreams. I am sleeping 1 -2 hours longer than normal. My level of anxiety is higher than normal. The fatigue was worse in the 2 weeks after the booster, but is still has not gone away.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma, high blood pressure
Andere Medikamente: Flovent, losartan
Allergien: Cats
Vorherige Impfungen: Fatigue and sleep disturbance after first 2 does of Pfizer Covid vaccine.

VAERS 1988634

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: OK
Alter: 57,0
Geschlecht: F
Eingang: 29.12.2021
Impfdatum: 13.12.2021
Beginn: 28.12.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: IM / LA

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

Cough Fatigue Paranasal sinus discomfort SARS-CoV-2 test positive

Symptomtext

FATIGUE, SINUS PRESSURE, DRY COUGH

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: 12/28/21: POSITIVE SARS COVID RAPID ANTIGEN
Aktuelle Erkrankungen: NONE
Vorgeschichte: DEPRESSION, HYPOTHYROIDISM, NEPHROCALCINOSIS, CONSTIPATION, HYPERLIPIDEMIA, GERD, VITAMIN D DEFICIENCY, LOW BACK PAIN, CKD STAGE 4
Andere Medikamente: LORATADINE, LEVOTHYROXINE, OMEPRAZOLE, ONDANSETRON, LOPERAMIDE, ATORVASTATIN, FLUOXETINE, EROCALCIFEROL
Allergien: NKA
Vorherige Impfungen: -

VAERS 1984733

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 46,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Disturbance in attention Fatigue Vision blurred

Symptomtext

I experienced fatigue, lack of concentration and blurry vision.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Antibiotics
Allergien: N/A
Vorherige Impfungen: -

VAERS 1983854

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: MA
Alter: 30,0
Geschlecht: F
Eingang: 28.12.2021
Impfdatum: 15.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: OT / LA

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

Arthritis Chest X-ray Dysphagia Hypersensitivity Rash Somnolence Streptococcus test Swelling Throat tightness Tonsillar inflammation X-ray

Symptomtext

inflamed joints/ inflammation in joints in both knees/ inflammation in joints in right ankle/ inflammation in joints in her foot/ inflammation in joints in both her thumbs/ inflammation in joints in her jaw; throat closing up; couldn't swallow; neck inflamed; tonsils inflamed; drowsy; rash on her forehead; allergic reaction; This spontaneous case was reported by a consumer and describes the occurrence of ARTHRITIS (inflamed joints/ inflammation in joints in both knees/ inflammation in joints in right ankle/ inflammation in joints in her foot/ inflammation in joints in both her thumbs/ inflammation in joints in her jaw), THROAT TIGHTNESS (throat closing up), DYSPHAGIA (couldn't swallow), SWELLING (neck inflamed) and TONSILLAR INFLAMMATION (tonsils inflamed) in a 30-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033f21a) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 15-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Nov-2021, the patient experienced ARTHRITIS (inflamed joints/ inflammation in joints in both knees/ inflammation in joints in right ankle/ inflammation in joints in her foot/ inflammation in joints in both her thumbs/ inflammation in joints in her jaw), THROAT TIGHTNESS (throat closing up), DYSPHAGIA (couldn't swallow), SWELLING (neck inflamed), TONSILLAR INFLAMMATION (tonsils inflamed), SOMNOLENCE (drowsy), RASH (rash on her forehead) and HYPERSENSITIVITY (allergic reaction). The patient was treated with METHYLPREDNISOLONE at a dose of 125 mg; DIPHENHYDRAMINE HYDROCHLORIDE (BENADRYL [DIPHENHYDRAMINE HYDROCHLORIDE]) for Allergic reaction, at an unspecified dose and frequency; METHYLPREDNISOLONE (MEDROL DOSEPAK) ongoing since an unknown date at an unspecified dose and frequency; HYDROXYZINE from 27-Nov-2021 to 30-Nov-2021 at an unspecified dose and frequency and IBUPROFEN at an unspecified dose and frequency. At the time of the report, ARTHRITIS (inflamed joints/ inflammation in joints in both knees/ inflammation in joints in right ankle/ inflammation in joints in her foot/ inflammation in joints in both her thumbs/ inflammation in joints in her jaw), THROAT TIGHTNESS (throat closing up), DYSPHAGIA (couldn't swallow), SWELLING (neck inflamed), TONSILLAR INFLAMMATION (tonsils inflamed), SOMNOLENCE (drowsy), RASH (rash on her forehead) and HYPERSENSITIVITY (allergic reaction) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 29-Nov-2021, Chest X-ray: normal (normal) Result: Patient reported Chest X-ray to look for blockages reported negative/normal.. On 29-Nov-2021, Streptococcus test: normal (normal) Result: Patient reported negative/normal strep test. On 29-Nov-2021, X-ray: normal (normal) Result: Patient reported Neck X-ray to look for blockages reported negative/normal.. Concomitant product use was not provided by the reporter. On 27 Nov 2021, Patient went to medical facility and was given 125 mg shot of methylprednisolone On 29 Nov 2021, Patient went to the Emergency Room and was tested for strep test, had a neck and chest X-Ray to look for blockages and got normal results Patient was given a prescription for hydroxyzine and took 2 of them on 27 Nov 2021 and one on 30 Nov 2021, but cannot take during the day because they make her drowsy. Company comment: This case concerns a 30-year-old, female patient with no medical history, who experienced the unexpected non serious events of arthritis, throat tightness, dysphagia swelling, tonsillar inflammation and somnolence and expected events of rash and hypersensitivity. The events occurred approximately 6 days after the third dose of mRNA-1273. As reported, the patient experienced a rash on her forehead, inflamed joints, and her throat closing up. She explained she had inflammation in her joints in both knees, her right ankle and foot, both of her thumbs and her ja. Patient stated her throat closing up as she couldn't swallow, her neck and tonsils were inflamed. Twelve days after vaccination she went to medical facility and was given a shot of methylprednisolone and two days later she went to the ER and was tested for strep, had a neck and chest xray to look for blockages. All came back negative/normal, as reported. The patient was given Benadryl to stop the allergic reaction and was also given a prescription for hydroxyzine which made her drowsy. She also took ibuprofen for pain. Considering the temporal relation of events and description of symptoms the case was assessed as non serious. Causality for somnolence was assessed as not related as hydroxyzine provides likely etiology. The benefit-risk relationship of mRNA-1273 is not affected by this report. This case was linked to MOD-2021-403081 (Patient Link).; Sender's Comments: This case concerns a 30-year-old, female patient with no medical history, who experienced the unexpected non serious events of arthritis, throat tightness, dysphagia swelling, tonsillar inflammation and somnolence and expected events of rash and hypersensitivity. The events occurred approximately 6 days after the third dose of mRNA-1273. As reported, the patient experienced a rash on her forehead, inflamed joints, and her throat closing up. She explained she had inflammation in her joints in both knees, her right ankle and foot, both of her thumbs and her ja. Patient stated her throat closing up as she couldn't swallow, her neck and tonsils were inflamed. Twelve days after vaccination she went to medical facility and was given a shot of methylprednisolone and two days later she went to the ER and was tested for strep, had a neck and chest xray to look for blockages. All came back negative/normal, as reported. The patient was given Benadryl to stop the allergic reaction and was also given a prescription for hydroxyzine which made her drowsy. She also took ibuprofen for pain. Considering the temporal relation of events and description of symptoms the case was assessed as non serious. Causality for somnolence was assessed as not related as hydroxyzine provides likely etiology. The benefit-risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: Test Date: 20211129; Test Name: Chest X-ray; Result Unstructured Data: Result: Patient reported Chest X-ray to look for blockages reported negative/normal.; Test Date: 20211129; Test Name: Streptococcus test; Result Unstructured Data: Result: Patient reported negative/normal strep test; Test Date: 20211129; Test Name: X-ray; Result Unstructured Data: Result: Patient reported Neck X-ray to look for blockages reported negative/normal.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1979219

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: IL
Alter: 39,0
Geschlecht: F
Eingang: 24.12.2021
Impfdatum: 26.11.2021
Beginn: 20.12.2021
Tage bis Beginn: 24,0
Dosis: 3
Route/Site: IM / -

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

Headache Nausea Respiratory tract congestion SARS-CoV-2 test negative

Symptomtext

Mild congestion, Positional headache, and mild nausea began 3am 12/20. Headache continued throughout day, spiking when I stood up (pain scale 7 or 8), and declining or going away completely when i laid down (pain scale 0-3) . By morning of 12/21 only mild headache remained (pain 1-2). Congestion decreased but not gone and mild headache coming and going since, but not dependent on movement. Covid rapid test on 12/22 negative. Mild headache still comes and goes as of 12/24, pain ranging from 1 to 3.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: N/A. Tried to schedule an e-visit with urgent care. They told me to go to urgent care or see my pcp. Since the headache has decreased in intensity, I scheduled an appointment. Have an appointment for jan 4, 2022 to see pcp.
Aktuelle Erkrankungen: 24 hr cold/flu bug, symptoms done 2 days before vaccine.
Vorgeschichte: Anxiety & depression; food sensitivities; occasional headaches, knee joint pain (recurrent)
Andere Medikamente: 30 mg fluoxetine; 200 mg Buproprion, mirena iud implant, xanax 0.5 mg (as needed), fish oil supplement
Allergien: Sulfa meds, twinrix vaccine, soy, corn, peanuts, wool, gluten and yeast sensitivity
Vorherige Impfungen: Twinrix, second dose in november 2011 during day. Anaphylaxis (throat closure, hives) that evening. Was advised against receiv

VAERS 1974637

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: PA
Alter: 66,0
Geschlecht: F
Eingang: 23.12.2021
Impfdatum: 21.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Inflammation Pruritus

Symptomtext

Inflammation (spreading with time) Itching

Weitere VAERSDATA-Felder

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

VAERS 1963997

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: VA
Alter: 63,0
Geschlecht: M
Eingang: 20.12.2021
Impfdatum: 09.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Angiogram Blood cortisol Blood glucose Blood test Electrocardiogram Full blood count Glomerular filtration rate Headache Magnetic resonance imaging head Ultrasound Doppler Urine analysis

Symptomtext

pain in head

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: doppler on 17th, ekg, a1c, cortyisol 30, 60, baseline, glucose, bubble study, cbc, metabolic panel, gfr, urine test, angiogram, mri brain,
Aktuelle Erkrankungen: -
Vorgeschichte: hypertension, type 2 diabetes, high cholesterol, autism
Andere Medikamente: cyclobenzapine, hcl, labetatol, lovastatn, melatonin, novalog, jardisnce, metformin, losartan, d3, childrens aspirin,
Allergien: -
Vorherige Impfungen: -

VAERS 1962508

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CT
Alter: 31,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 19.11.2021
Beginn: 03.12.2021
Tage bis Beginn: 14,0
Dosis: 3
Route/Site: SYR / LA

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

Chronic spontaneous urticaria

Symptomtext

Ongoing chronic spontaneous urticaria presenting 12/3/2021 (two weeks after vaccine administered). Rash disappears and reappears in different random locations (scalp, neck, back, stomatch, behind ears). Oral administration of Zyrtec relieves symptoms for approx. 24 hours, but symptoms return when daily dosage is halted. No known existing allergies. No reactions to the first two moderna shots, only to the booster. Will seek a clinic visit soon, but has not had time yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chronic spontaneous urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Hemangiomae on right arm
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Fever in response to various vaccines (TDAP, Moderna COVID-19) on various dates

VAERS 1962471

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MI
Alter: 27,0
Geschlecht: F
Eingang: 19.12.2021
Impfdatum: 22.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: SYR / LA

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

Ear discomfort Flushing Hypersensitivity Mechanical urticaria Pruritus Rash Urticaria

Symptomtext

On the night of Dec. 1st, I went to bed with extremely itchy palms of my hands and feet; I had never experienced a burning itch like this before. On Dec. 2, I awoke with hives on my lower back and abdomen and went to urgent care. I was given a steroid injection and a course of prednisone. The urgent care doctor suspected a contact allergy or Rash. The following day, my ears were flushed, I had small hives around my eyes, and hives on the base of my neck. I called my primary care physician but was seen by a PA who could not make a diagnosis but suspected an allergic reaction to ?something.? Over the past 17 days, I have noticed that the hives are induced by the slightest scratch against my skin (dermatographia). Claritin seems to alleviate the itching and burning ears slightly. I have not changed my diet, detergent, no new animals, no new foods, etc. I have never had a reaction like this before. The itching and burning is extreme. I have found a few internet posts of delayed uticaria with covid vaccination. Thus, since I am unable to identify any other trigger, my suspect is the booster I had.

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Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Lexapro Klonopin Multivitamin
Allergien: Ciproflaxicin-extreme fatigue and stomach pain
Vorherige Impfungen: -

VAERS 1962385

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: SC
Alter: 84,0
Geschlecht: M
Eingang: 19.12.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain

Symptomtext

Patient experiencing pain at injection site/arm almost up to a month after the taking the vaccine. Reported to the pharmacy. Pharmacist advised patient to see a Doctor for treatment.

Weitere VAERSDATA-Felder

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

VAERS 1959311

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21A

mild

Staat: CT
Alter: 41,0
Geschlecht: F
Eingang: 17.12.2021
Impfdatum: 01.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: - / LA

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

Injection site discolouration

Symptomtext

White spot where booster was given. Still there 2 weeks later.

Weitere VAERSDATA-Felder

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

VAERS 1959263

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: SC
Alter: 65,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 05.11.2021
Beginn: 28.11.2021
Tage bis Beginn: 23,0
Dosis: 3
Route/Site: IM / RA

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

Dizziness Interchange of vaccine products Loss of personal independence in daily activities Vertigo

Symptomtext

Three weeks and 2 days after the booster injection, I woke to severe vertigo symptoms. My first 2 injections in April & May 2021 were Pfizer, while my booster was Moderna (recommended by CDC that the booster may be more effective if different from the original brand of injections. It has now been almost 3 weeks and the vertigo symptoms are almost always still with me. I am learning how to function, carefully, so that most daily activities are somewhat manageable.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: Office examination by primary care physician revealed no active sinus or ear infections, so only a prescription of Meclezine 25mg was given, which doesn't help the dizziness or room "spinning", but makes me sleepy.
Aktuelle Erkrankungen: None.
Vorgeschichte: Loss of knee cartilage - knee pain (6 or 7 years).
Andere Medikamente: Clonazepam 0.5 mg Zyrtec for Allergies
Allergien: Some adhesives.
Vorherige Impfungen: -

VAERS 1955960

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CT
Alter: 40,0
Geschlecht: M
Eingang: 16.12.2021
Impfdatum: 04.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / LA

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

Pruritus Rash Swelling face Urticaria

Symptomtext

Severe Hives/Rash and itchiness. Started slow and isolated and then expanded each day until my entire body was covered including hands and feet. Lasted for a few days and then my entire face swelled. On steroids and antihistamine for weeks until it mostly but not completely went away. Still isolated itching, especially overnight (4 weeks after it began).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Minor Psoriasis
Andere Medikamente: Vitamin D, Fish Oil, pantoprazole
Allergien: Amoxicillin
Vorherige Impfungen: -

VAERS 1955953

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NH
Alter: 42,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 16.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / LA

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

Angioedema Full blood count Neutrophil count Pruritus Tryptase Urticaria

Symptomtext

Full body large urticarial plaques and severe pruritus on Day 11 after booster. Necessitated urgent allergist visit. Some mild angioedema but no anaphylaxis. High dose antihistamines (Allegra 120mg QAM , Zyrtec 20mg QPM, ranitidine 10mg midday) were effective. Now 3 weeks into the eruption and still with some hives, albeit many fewer. Still taking Allegra 180mg daily.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: CBC wnl aside from neutrophilia Complement levels and tryptase wnl
Aktuelle Erkrankungen: None
Vorgeschichte: No history of anaphylaxis +h/o Atopy (atopic dermatitis and environmental allergies to dust, mold, cats, horses)
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1955659

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NY
Alter: 24,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 16.11.2021
Beginn: 12.12.2021
Tage bis Beginn: 26,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Fatigue Headache Illness Impaired work ability Loss of personal independence in daily activities Oropharyngeal pain Respiratory tract congestion SARS-CoV-2 test positive Sneezing Upper-airway cough syndrome

Symptomtext

Symptomatic COVID-19 infection. Symptoms started on 12/11 with very slight non-productive cough, escalated to headache, cough, sneezing, congestion, and sore throat from post nasal drip on 12/13. Had to cancel doctors appointments due to quarantine until 12/22. Was unable to work or perform household chores from 12/13-12/15 due to illness. Symptoms almost completely resolved by 12/16 other than fatigue.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: Nasal swab resulting in positive PCR result on 12/14.
Aktuelle Erkrankungen: None
Vorgeschichte: Major depressive disorder Heart murmur
Andere Medikamente: Spironolactone 50 mg BID (100 mg total daily) Effexor 150 mg QD Buspar 15 mg QD Tri Lo Sprintec QD Metformin 15 mg QD
Allergien: No allergies
Vorherige Impfungen: -

VAERS 1954968

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NY
Alter: 59,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Pain in extremity

Symptomtext

PATIENT REPORTED THAT SHE IS STILL HAVING A SORE ARM/JOINT/SHOULDER PAIN 1 MONTH AFTER SHE RECEIVED HER VACCINE. THE PHARMACIST GAVE HER A BOTTLE OF APAP AND NAPROXEN.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: Shoulder surgery
Vorgeschichte: Shoulder surgery
Andere Medikamente: -
Allergien: Cephalexin, Bupropion
Vorherige Impfungen: -

VAERS 1952682

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CA
Alter: 28,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 10.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: SYR / LA

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

Urticaria

Symptomtext

13 days post moderna booster got random hives all over my body. they have been happening daily in random spots ever since. went to urgent care on 12/3 put me on prednisone zyrtec pepcid and benadryl for a week. that seemed to help but the symptoms returned once prednisone was stopped and are still ongoing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: urgent care gave me prednisone on 12/3. they did not believe it was due to the booster but what do they know lol
Aktuelle Erkrankungen: None
Vorgeschichte: Interstitial cystitis
Andere Medikamente: Fish oil, vitamin d, vitamin b12, iron
Allergien: None
Vorherige Impfungen: -

VAERS 1951778

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21a

mild

Staat: VA
Alter: 55,0
Geschlecht: F
Eingang: 15.12.2021
Impfdatum: 27.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / RA

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

Fatigue Headache Influenza like illness Pyrexia

Symptomtext

Flu-like symptoms 12 hours after the 2nd dose of the Moderna vaccine. Fever, headache, fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Allergies/Asthma (mild)
Vorgeschichte: Osteoporosis
Andere Medikamente: Zyrtec D HRT-Amabalez Estradiol-Noreth 0.5-0.1 mg Wellbutrin XL 300 mg Singular Valacyclovir
Allergien: Neosporin
Vorherige Impfungen: -

VAERS 1947785

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: -
Alter: 73,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 29.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Basal cell carcinoma Biopsy skin abnormal Pain Rash macular Surgery Suture insertion

Symptomtext

After the booster was just soreness. Spots on left calf and right leg shin took 25 stiches to close the wound on my surgery on 19 Dec2021. It going to take another month to heal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain
Hospital-Tage: -
Labordaten: Biopsy - Basil cell on right shin
Aktuelle Erkrankungen: No
Vorgeschichte: High Blood Pressure and Hypertension
Andere Medikamente: Low Dose Aspirin, Zinc ,Metamucil, Iron, Calcium
Allergien: Thimerosal - contact solution
Vorherige Impfungen: Flu shot when I was a teenage - dizzy and passed out. both 1st and 2nd Moderna - night sweats and chills and diarrhea for about

VAERS 1947593

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 29,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 15.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / AR

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

Erythema Mechanical urticaria Pruritus Swelling Urticaria

Symptomtext

Dermatographia - about 10 days after my vaccine, I noticed I was becoming itchy in multiple areas of the body, including the scalp. When I checked the areas I was itching, there was a raised area similar to hives, surrounded by erythema/redness. This area of redness lasts about 30-45 minutes. If I stroke my skin or scratch it in a line, there will appear an exact area of redness, in the pattern of the scratching, about 5-10 minutes after the initial contact with the skin. I experience a general itching sensation throughout the day and the sensation increases if I scratch the area.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Seasonal Affective Disorder (MDD with seasonal features)
Andere Medikamente: Escitalopram 10mg; Multi-vitamin
Allergien: Hazelnut
Vorherige Impfungen: -

VAERS 1945315

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MD
Alter: 37,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 04.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 13,0
Dosis: 1
Route/Site: - / RA

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

Burning sensation Pruritus Skin warm Urticaria

Symptomtext

Very Itchy hives in random places of my body. Hives have burning sensation, hot to the touch and unbearably itchy. Hives appear for 15 minutes in a random spot of my body like arm or neck or leg and then disappear. They appear on some other spot randomly. Gets worse at night. Affects my sleep badly. Claritin helps for 24 hours but then the hives come back.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Non
Aktuelle Erkrankungen: Non
Vorgeschichte: Non
Andere Medikamente: One-a-day Women multi vitamin
Allergien: Non
Vorherige Impfungen: -

VAERS 1945107

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NY
Alter: 25,0
Geschlecht: M
Eingang: 13.12.2021
Impfdatum: 23.11.2021
Beginn: 03.12.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: IM / -

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

Arthralgia Arthropod bite Dysphagia Erythema Pain in extremity Peripheral swelling Pruritus Rash Urticaria

Symptomtext

Starting on 12/3/2021, I started to get slight itching at the back of my head. I had assumed it was a regular rash or mosquito bite. On 12/4/2021, I broke out in full body hives, accompanied by itchiness as well. I also experienced slight swelling in the hands, and arm soreness where the hives were. Overnight 12/4/2021 in 12/05/2021 I had difficulty swallowing as well. This lasted until 12/06/2021. Then, on 12/08/2021, the hives continued to intensify into hand/joint pain. The pain was more intense in the same arm as I received my Moderna booster shot. I could barely close my hand, along with the joint pain, inflammation, and redness. I proceeded to the ER on 12/08/2021 which is when they said it could be from the vaccine and diagnosed me with urticaria. They prescribed Prednisone 40mg over the course of four days. Over these four days it did seem to make the itching go away, but the redness, and hives were still consistent. Today is 12/13/2021 and I am still experiencing full body hives and redness, which I have never had in my life. I also have no allergy history, or a history of skin conditions.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None - I am uninsured until 01/01/2022 and am unable to get testing.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: -

VAERS 1944882

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: TX
Alter: 41,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 19.11.2021
Beginn: 04.12.2021
Tage bis Beginn: 15,0
Dosis: 3
Route/Site: SYR / LA

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

Mechanical urticaria Pruritus Urticaria

Symptomtext

Spontaneous hives appeared the night of 12/4 that spread across entire body. The hives come and go and move around but are always there and have persisted every day since. I am also experiencing dermatographia. Taking Xyzal helps manage the hives but it does not completely stop the itching.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: No tests yet
Aktuelle Erkrankungen: N/A
Vorgeschichte: Hypothyroidism
Andere Medikamente: Levothyroxine Birth control Rosuvastatin
Allergien: N/A
Vorherige Impfungen: -

VAERS 1943609

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: OK
Alter: 27,0
Geschlecht: F
Eingang: 13.12.2021
Impfdatum: 22.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: IM / LA

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

Pruritus Urticaria

Symptomtext

Hives and itchiness-starting 8 days after booster. Took Benadryl and was prescribed a Medrol Pak. Symptoms have continuously improved, however, they are not 100% gone yet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Saw Doctor. He prescribed me with a Medrol Pak.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None that are known
Vorherige Impfungen: -

VAERS 1942514

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MN
Alter: 45,0
Geschlecht: F
Eingang: 12.12.2021
Impfdatum: 18.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

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

Extra dose administered Urticaria

Symptomtext

Hives all over trunk, started two weeks after booster, no other changes in life, 5 days of prednisone improved symptoms but they are still lingering

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: No tests just visual inspection
Aktuelle Erkrankungen: None
Vorgeschichte: Hypothyroid, HTN, fibromyalgia
Andere Medikamente: Levothytoxine. Metoprolol succinate
Allergien: NKDA
Vorherige Impfungen: Moderna age 44 swollen pinky finger 1-13-21

VAERS 1940263

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 56,0
Geschlecht: M
Eingang: 10.12.2021
Impfdatum: 29.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / -

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

Arthralgia Enteritis Gait inability Joint swelling Platelet count increased Rash White blood cell count increased

Symptomtext

After receiving the booster (3rd) dose of moderna covid vaccine on 11/29/21, the patient began to develop a rash a few days later. The rash worsened, so patient went to his PCP who put him on oral steroids. A few days later the patient developed enteritis and was admitted to this hospital. He was hospitalized for 5 days/4 nights and then released home. He returns today with significant swelling and pain in multiple joints - unable to ambulate.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: 5,0
Labordaten: WBC 15.9 Plt 586 All else, so far, within normal limits
Aktuelle Erkrankungen: None
Vorgeschichte: Hyperlipidemia Depression
Andere Medikamente: Lipitor 40mg nightly Wellbutrin XL 300mg daily Pepcid 20mg twice a day Zoloft 100mg daily
Allergien: Prilosec
Vorherige Impfungen: -

VAERS 1940250

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 66,0
Geschlecht: F
Eingang: 10.12.2021
Impfdatum: 16.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: SYR / LA

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

Arthralgia Asthenia Chills Decreased appetite Fatigue Headache Influenza virus test negative Micturition disorder Myalgia Pain Pyrexia SARS-CoV-2 test negative

Symptomtext

I had body ache and tired. Then I had headache, chills, joint and muscle pains all over. I lost my appetite and had no energy. I had lower-grade fever. I had fatigue. My urine discharge felt different. I went to urgent care to get tested for COVID-19 and Flu, negative results.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: COVID-19 Test; Flu Test
Aktuelle Erkrankungen: N/A
Vorgeschichte: Synesis
Andere Medikamente: Valsartan; Rosuvastatin; Baby Aspirin
Allergien: Decillion; Sofia drug
Vorherige Impfungen: -

VAERS 1936424

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: DE
Alter: 51,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 10.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 9,0
Dosis: 3
Route/Site: - / RA

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

Contusion Lip swelling Peripheral swelling Pruritus Swelling face Urticaria

Symptomtext

large bruise on arm 7 days later. on 17th got severe itching on stomach, feet, and legs. broke out in hives everywhere, spreading severely to the point where they started touching. progressed through weekend, developed swelling face, lips, and feet.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: hypothyroidism
Andere Medikamente: synthroid, prevacid, vitamins
Allergien: -
Vorherige Impfungen: -

VAERS 1936389

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: SC
Alter: 76,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 04.03.2021
Beginn: 05.03.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site erythema Injection site swelling

Symptomtext

Left arm swollen and beat red from shoulder to elbow. Treated with steroid cream with itching.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: Saw NP a few days/week later for it and she prescribed the steroid cream.
Aktuelle Erkrankungen: allergic reaction to prednisone drops used during eye surgery
Vorgeschichte: Fibromyalgia with chronic fatigue syndrome, post-surgical thyroid removal, hypoglycemic
Andere Medikamente: herbal supplements from Harrisburg, multi-vitamins, magnesium, potassium, malic acid,
Allergien: PCN, Keflex, Codeine, Prednisone
Vorherige Impfungen: -

VAERS 1936104

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 57,0
Geschlecht: M
Eingang: 09.12.2021
Impfdatum: 30.10.2021
Beginn: 06.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Pruritus Urticaria

Symptomtext

Hives and severe itching began about one week after vaccination. I suspected I had an allergic reaction to something, but could not identify the cause. I had been away at a hotel and had been hiking the weekend the symptoms started. At the time I had no reason to believe it could have been a delayed reaction to the vaccination so I did not report it to my doctor. My Doctor's assessment & treatment is given below: Raised urticarial lesion over left armpit, bilateral wrists and forearms, groin and waist band and popliteal fossa and back of his bilateral legs. (Note: actually was both armpits) Start Prednisone Tablet, 20 MG, 3 x 3 days then 2 x 3 days then 1 x 3 days then off Notes: will treat with pred and antihitamine and rtc if ineffective. I've had a reaction like this before to poison ivy, but the poison ivy rash was evident prior to the urticaria. In that case, the poison ivy rash and urticaria both resolved quickly (a few days) once I started taking the Prednisone. In the recent case, the severe itching and urticaria was significantly reduced within a few days, but minor itching and urticaria continue to this day. It is slowly getting better, but I am still taking antihistamines (Claritin and/or benadryl) daily. Some research indicated that this could have been a delayed, non-allergic reaction to the vaccination. My doctor agreed that this was a possibility and recommended that I continue the antihistamines until the symptoms resolve. I also want to note that after the second dose and the booster dose of the Moderna Vaccination I also had the more typical reactions of a sore arm, headache, fever (~100F) and fatigue, which started the following morning after the vaccination and lasted about 24 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: hypercholesterolemia, Pre-Diabetic (A1C 6.0), GERD
Andere Medikamente: Pravastatin40mg, Famotidine20mg, Magnesium250mg, Men's 1-A-Day
Allergien: Diclofenac, Latex, Poison Ivy
Vorherige Impfungen: -

VAERS 1935854

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NY
Alter: 27,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 19.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: - / -

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

Erythema Pruritus Urticaria

Symptomtext

Generalized itching, flare ups of redness on arms. back and legs, and hives.

Weitere VAERSDATA-Felder

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

VAERS 1935661

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MD
Alter: 24,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 06.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 1,0
Dosis: UNK
Route/Site: IM / -

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

Injection site pain Injection site pruritus Injection site reaction Injection site warmth Rash erythematous

Symptomtext

red rash under vaccine site, itchiness, rash is tender and warm to touch

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: colitis
Vorgeschichte: hypothyroidism
Andere Medikamente: Synthroid, 25mcg tri-lo-marzia birth control
Allergien: bactrium doxycycline allergies
Vorherige Impfungen: -

VAERS 1935302

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 63,0
Geschlecht: F
Eingang: 09.12.2021
Impfdatum: 02.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: OT / -

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

Back pain Magnetic resonance imaging Red blood cell count Spinal cord infection White blood cell count

Symptomtext

Staph infection in her spinal canal; excruciating pain in her lower back area; This spontaneous case was reported by a consumer and describes the occurrence of SPINAL CORD INFECTION (Staph infection in her spinal canal) and BACK PAIN (excruciating pain in her lower back area) in a 63-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 09-Nov-2021, the patient experienced BACK PAIN (excruciating pain in her lower back area) (seriousness criterion hospitalization). On 12-Nov-2021, the patient experienced SPINAL CORD INFECTION (Staph infection in her spinal canal) (seriousness criteria hospitalization and medically significant). The patient was hospitalized from 09-Nov-2021 to 16-Nov-2021 due to BACK PAIN and SPINAL CORD INFECTION. The patient was treated with CEFAZOLIN ongoing since an unknown date for Antibiotic therapy, at a dose of UNK, q8h for the next 12 weeks and Surgery (An Emergency surgery to remove staph from her spinal.) for Spinal cord infection. At the time of the report, SPINAL CORD INFECTION (Staph infection in her spinal canal) and BACK PAIN (excruciating pain in her lower back area) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 12-Nov-2021, Magnetic resonance imaging: abnormal (abnormal) Staph infection in spinal canal and abnormal (abnormal) Staph infection in spinal canal. On an unknown date, Red blood cell count: 8 (Low) 8. On an unknown date, White blood cell count: 1800 (High) 1800. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. Patient called to report that she received her Moderna booster on 02NOV2021. On 09NOV2021 patient reported that she was rushed to the hospital with excruciating pain in her lower back area. After two MRI's on 12NOV2021, it was discovered that patient had a Staph infection in her spinal canal. They did an Emergency surgery to remove staph from her spinal canal. She also stated that her white blood count was through the roof (1800) and her red blood cells were low (8) but are coming up. Patient further reported that she is taking antibiotic home infusion therapy called Cefazolin. She has to take infusions every 8 hours for the next 12 weeks. Patient also stated the antibiotic therapy was helping. She reported she was admitted to the hospital on 09NOV2021 and discharged 16NOV2021. Patient plans to see a Hematologist on 30NOV2021. Lot Number #: 033F21A, Expiration date: Unknown Company Comment: This case concerns a 63-year-old female patient with no relevant medical history, who experienced the serious unexpected events of Back Pain and Spinal Cord Infection. The events, which caused hospitalization to the patient, occurred approximately 7-10 days after receiving the third dose of mRNA-1273 Vaccine. During hospitalization, the patient's white blood cell count was elevated, and red blood cell count decreased. MRI revealed Staph infection her spinal canal and then underwent emergency surgery to treat the spinal canal infection. Patient was hospitalized for 5 days then discharged with home medications. The rechallenge was not applicable since only information about the third dose was disclosed. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.; Sender's Comments: This case concerns a 63-year-old female patient with no relevant medical history, who experienced the serious unexpected events of Back Pain and Spinal Cord Infection. The events, which caused hospitalization to the patient, occurred approximately 7-10 days after receiving the third dose of mRNA-1273 Vaccine. During hospitalization, the patient's white blood cell count was elevated, and red blood cell count decreased. MRI revealed Staph infection her spinal canal and then underwent emergency surgery to treat the spinal canal infection. Patient was hospitalized for 5 days then discharged with home medications. The rechallenge was not applicable since only information about the third dose was disclosed. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Back pain
Hospital-Tage: 8,0
Labordaten: Test Date: 20211112; Test Name: MRI; Result Unstructured Data: Staph infection in spinal canal; Test Date: 20211112; Test Name: MRI; Result Unstructured Data: Staph infection in spinal canal; Test Name: RBC; Result Unstructured Data: 8; Test Name: WBC; Result Unstructured Data: 1800
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1933825

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NY
Alter: 37,0
Geschlecht: M
Eingang: 08.12.2021
Impfdatum: 28.11.2021
Beginn: 06.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / LA

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

Urticaria

Symptomtext

Hives all over my body.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Urticaria
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Mild psoriasis
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: Feverish and weak after second moderna Covid-19 vaccine. Lot 040B21A

VAERS 1932697

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 41,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 03.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / RA

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

Erythema Fatigue Lymphadenopathy Oropharyngeal pain Sensory disturbance

Symptomtext

I went in to get my booster and felt the liquid go up into my shoulder and up neck, into my skull. On Monday, 12/6, after my shower in the morning, my lymph nodes were swollen and I was very tired; with a sore throat. I noticed there was redness on my lymph nodes, which died down in the same day. Today, on 12/8, my throat is sore and my lymph nodes are still swollen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Almopodine 5/mg daily Singulair 10/mg daily Prevacid OTC daily
Allergien: No
Vorherige Impfungen: -

VAERS 1932124

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: IN
Alter: 54,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 03.12.2021
Beginn: 03.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Cough Diarrhoea Fatigue Headache Nausea Oropharyngeal pain Pain Pyrexia

Symptomtext

On the day of of the vaccine, I experienced Nausea and a head ache. The following 2 days I experienced body aches and fatigue. On the third day after the vaccine I experienced chills, low grade fever (99.5), diarrhea, fatigue, body aches, sore throat, and a cough. On day 4, I still feel very tired, exhaust easily, minor body aches, sore throat, and a mild cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: NA
Aktuelle Erkrankungen: NA
Vorgeschichte: High cholesterol
Andere Medikamente: Provastatin 20mg Fish Oil 1200mg Culturelle Probiotic
Allergien: Ingested iodine Penicillin Morphine
Vorherige Impfungen: -

VAERS 1931428

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NY
Alter: 53,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 12.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 19,0
Dosis: 1
Route/Site: OT / RA

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

Blood potassium increased Muscular weakness Musculoskeletal stiffness Myalgia Pain in extremity Peripheral swelling Swelling

Symptomtext

muscles felt weak; muscles felt a bit tender; the left arm felt like it had had a shot, it was a little bit sore; left arm was a little bit swollen; clavicle area started to swelled up on the opposite side from the shot, from the neck all the way down. it was super-swollen.; neck was stiff; This spontaneous case was reported by a consumer and describes the occurrence of MUSCULOSKELETAL STIFFNESS (neck was stiff), SWELLING (clavicle area started to swelled up on the opposite side from the shot, from the neck all the way down. it was super-swollen.), MUSCULAR WEAKNESS (muscles felt weak), MYALGIA (muscles felt a bit tender) and PAIN IN EXTREMITY (the left arm felt like it had had a shot, it was a little bit sore) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Migraine. Concomitant products included TOPIRAMATE (TOPAMAX) for Migraine, BUPROPION HYDROCHLORIDE (WELLBUTRIN) and VITAMINS NOS for an unknown indication. On 12-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 01-Dec-2021, the patient experienced MUSCULOSKELETAL STIFFNESS (neck was stiff). On 02-Dec-2021, the patient experienced SWELLING (clavicle area started to swelled up on the opposite side from the shot, from the neck all the way down. it was super-swollen.). On 05-Dec-2021, the patient experienced MUSCULAR WEAKNESS (muscles felt weak), MYALGIA (muscles felt a bit tender), PAIN IN EXTREMITY (the left arm felt like it had had a shot, it was a little bit sore) and PERIPHERAL SWELLING (left arm was a little bit swollen). The patient was treated with ASPIRIN [ACETYLSALICYLIC ACID] ongoing since an unknown date at an unspecified dose and frequency. At the time of the report, MUSCULOSKELETAL STIFFNESS (neck was stiff), SWELLING (clavicle area started to swelled up on the opposite side from the shot, from the neck all the way down. it was super-swollen.), MUSCULAR WEAKNESS (muscles felt weak), MYALGIA (muscles felt a bit tender), PAIN IN EXTREMITY (the left arm felt like it had had a shot, it was a little bit sore) and PERIPHERAL SWELLING (left arm was a little bit swollen) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood potassium increased: high (High) high. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Patient consulted with their HCP, who indicated a sonogram of the head and neck area. Patient is scheduled to get the Moderna second dose on Friday 10Dec2021 and wonder if they should get it, wait or not get it at all.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: Test Name: high level of potassium; Result Unstructured Data: high
Aktuelle Erkrankungen: Migraine
Vorgeschichte: -
Andere Medikamente: WELLBUTRIN; TOPAMAX; VITAMINS NOS
Allergien: -
Vorherige Impfungen: -

VAERS 1931317

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 08.12.2021
Impfdatum: 26.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Arthralgia Chills Eye irritation Feeling cold Headache Lacrimation increased Myalgia Nausea

Symptomtext

Felt burning around left eye; left eye was watering; Feel constantly cold; muscles from arms and legs feeling like burning, lower back like burning and and now went up to the head; nausea; headache/head is killing; chills; joint pain in upper left arm and knees; This spontaneous case was reported by a consumer and describes the occurrence of EYE IRRITATION (Felt burning around left eye), LACRIMATION INCREASED (left eye was watering), FEELING COLD (Feel constantly cold), MYALGIA (muscles from arms and legs feeling like burning, lower back like burning and and now went up to the head) and NAUSEA (nausea) in a 58-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Previously administered products included for Product used for unknown indication: Pfizer-BioNTech COVID-19 Vaccine (lot number - ER8727) on 24-Mar-2021 and Pfizer-BioNTech COVID-19 Vaccine (lot number - EW0153) on 14-Apr-2021. Past adverse reactions to the above products included No adverse event with Pfizer-BioNTech COVID-19 Vaccine and Pfizer-BioNTech COVID-19 Vaccine. On 26-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced EYE IRRITATION (Felt burning around left eye), LACRIMATION INCREASED (left eye was watering), FEELING COLD (Feel constantly cold), MYALGIA (muscles from arms and legs feeling like burning, lower back like burning and and now went up to the head), NAUSEA (nausea), HEADACHE (headache/head is killing), CHILLS (chills) and ARTHRALGIA (joint pain in upper left arm and knees). The patient was treated with IBUPROFEN at a dose of 800 milligram; 1 or 2. At the time of the report, EYE IRRITATION (Felt burning around left eye), LACRIMATION INCREASED (left eye was watering), FEELING COLD (Feel constantly cold), MYALGIA (muscles from arms and legs feeling like burning, lower back like burning and and now went up to the head), NAUSEA (nausea), HEADACHE (headache/head is killing), CHILLS (chills) and ARTHRALGIA (joint pain in upper left arm and knees) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported.

Weitere VAERSDATA-Felder

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

VAERS 1930032

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MO
Alter: 40,0
Geschlecht: F
Eingang: 07.12.2021
Impfdatum: 05.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Chills Extra dose administered Interchange of vaccine products Pruritus Pyrexia Rash

Symptomtext

skin rash transversing neck, chest and stomach area. Slighly itchy. Took 25 mg of benadryl. Onset about 50 hours post vaccine. Fever and chills present day prior and morning of. Of note: dose 1 and 2 were Pfizer and rash occured

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: one a day women's daily vitamin sertaline vitamin D
Allergien: none
Vorherige Impfungen: -

VAERS 1926077

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: VA
Alter: 39,0
Geschlecht: M
Eingang: 06.12.2021
Impfdatum: 03.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: IM / RA

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

Anti-thyroid antibody Antinuclear antibody Blood immunoglobulin E Differential white blood cell count Full blood count Mechanical urticaria Metabolic function test Peripheral swelling Platelet count Pruritus Red blood cell sedimentation rate Sensitive skin Sleep disorder Swelling Swelling face Urticaria

Symptomtext

3rd shot, booster on Nov 3rd. 11 days later on Nov 14th started getting hives all over body. Swelling. Itchyness. Unable to sleep due to intense itchnyess. Saw various allergists and even an ER visit when my face started swelling up. Finally immunologist put me on high doses of zyrtec/pepsid + steroids seemed to control symptoms, although I still have swelling in my face and very sensitive skin (dermatographism) Now, 3 weeks out from symptoms, a month since taking the 3rd booster shot, I'm still having the same symptoms, but managing with high doses of anti-histamines, steroids and a PPI. If I stop the medication, I have itchyness, hives, swelling in hands and feet, face.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: After my followup with immunologist today (dec 6th), we ordered the following: Thyroid Peroxidase (Tpo) Ab Thyroglobulin Antibody Sed Rate, Westergren ANA W/reflex If Positive-164863-P CBC with Differential/platelet Comp. Metabolic Panel (14)-322000-P anti-IgE* 12/06/2021 Labcorp Allergens W/total IgE Area 2
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Cats
Vorherige Impfungen: -

VAERS 1925101

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CA
Alter: 29,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 08.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 11,0
Dosis: 3
Route/Site: SYR / LA

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

Allergy test Blood test Mechanical urticaria Pruritus Swelling Urticaria

Symptomtext

11/18 Extreme Itching in the middle of night. Hives on neck and face in the morning. 11/19 Hives over several different parts of body. Visit with the Urgent Care. Was informed to take Zyrtec and use steroid cream on hives. 11/20 Swelling of the right ear, lips, forehead, scalp, hands, feet. 11/21 Zyrtec keeping most symptoms away. Ear, lip, scalp swelling go away. Hand and Feet swelling remain. Develop symptoms of Dermatographia. 11/24 Hand and Feet swelling cease. 11/25-Today (12/6) Occasional Hives that come and go. Dermatographia remains.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mechanical urticaria
Hospital-Tage: -
Labordaten: Waiting on blood allergy panel results
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Birth Control
Allergien: none
Vorherige Impfungen: -

VAERS 1925044

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 36,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 15.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 2,0
Dosis: 2
Route/Site: IM / LA

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

Nausea Nipple disorder Pain in extremity Pruritus Vomiting

Symptomtext

11/17 symptoms began 48 hours after the vaccination. Patient's arm was sore (left). Patient felt nauseous and did vomit for one week. Patient also has severe itching on her arm and upper chest specifically her nipple. Her nipples (both) are itchy and she has put lotion on her chest area but has not helped. Pt. has taken vitamin E capsules and cut them in half and placed on her nipples for relief for dryness. No trouble breathing, no chest pain. She has not yet seen a doctor yet but is going to see her PCP.

Weitere VAERSDATA-Felder

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

VAERS 1924552

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MO
Alter: 27,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 01.12.2021
Beginn: 02.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Injection site erythema Injection site pruritus Injection site swelling Injection site warmth Musculoskeletal stiffness Pain in extremity

Symptomtext

The morning after the booster was administered, the left arm became stiff, sore, and noticeably swollen near the injection site. Symptoms peaked the evening of December 2, 2021, with a large red area (hives-like in appearance) around the injection site, with a diameter of about 4 inches. The red area was hot to the touch, and was mildly itchy. Swelling and heat reduced considerably by the afternoon of December 3. Redness and itching persisted until the evening of December 5. No such symptoms were experienced with dose 1 or 2 of the Moderna vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Adderall 10 MG Fluoxetine HCL 10 MG Tirosint
Allergien: N/A
Vorherige Impfungen: -

VAERS 1924253

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: MA
Alter: 27,0
Geschlecht: F
Eingang: 06.12.2021
Impfdatum: 07.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: - / -

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

Erythema Laboratory test normal Liver function test normal Pruritus Rash Renal function test normal Skin swelling Urticaria

Symptomtext

My skin is very itchy. There is no rash, but when I itch my skin becomes red and swollen. Hives will appear after my skin is itched. I have seen the ER and an urgent care. They have given me prednisone which doesn?t really help. Zyrtec and Benadryl make me less itchy but the skin rash still appears if I itch. Eucerin / ice packs helps relieve itching once itched

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Lab tests were done to check liver and kidney function. All results came back normal. I can provide pdfs of lab work if needed. Lab work was done 11/19 and 12/4.
Aktuelle Erkrankungen: None
Vorgeschichte: Celiac Hypothyroidism
Andere Medikamente: Levothyroxine Kelnor Iron Vitamin b Multivitamin Omega Probiotic Mitochondria ATP Calcium magnesium
Allergien: Gluten
Vorherige Impfungen: -

VAERS 1923427

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: GA
Alter: 64,0
Geschlecht: F
Eingang: 04.12.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Erythema Pyrexia

Symptomtext

Fever (101+), red arm, and chills; currently recovered and fine now.

Weitere VAERSDATA-Felder

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

VAERS 1923412

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: GA
Alter: 54,0
Geschlecht: M
Eingang: 04.12.2021
Impfdatum: 24.11.2021
Beginn: 25.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Diarrhoea Headache Herpes zoster Malaise Musculoskeletal stiffness Oropharyngeal pain Pain of skin SARS-CoV-2 test negative Streptococcus test negative

Symptomtext

Got shot at 3 pm on 11/24/2021. Had sore throat, stiff neck, headache and sore areas of scalp by 8 am next morning. Travelled for work on 11/29/2021 and saw Urgent Care in another city. Prescriped Lidocane for the sore throat. Returned home on 12/1 still not feeling well. Developed clear sores on scalp on 12/2. Developed shooting headaches and diarrhea on morning of 12/4. Diagnosed with Shingles at 4:00 pm on 12/4.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Strep throat and COVID-19 tests. Both negative.
Aktuelle Erkrankungen: None
Vorgeschichte: High blood pressure, high cholesterol, low testosterone, restless leg, anxiety
Andere Medikamente: Anastrozole, Atenolol, Atorvastatin, Buspirone, Cabergoline, HCG, Lisinopril, Melatonin, Omeprazole, Ropinirole, Tadalafil, Tesosterone
Allergien: None
Vorherige Impfungen: -

VAERS 1921431

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: CA
Alter: 67,0
Geschlecht: M
Eingang: 03.12.2021
Impfdatum: 22.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Asthenia Blood test Decreased appetite Dizziness Nausea Pain in extremity Pyrexia Somnolence

Symptomtext

sore arm, fever, naseua, weakness, dizziness, loss of appetite, sleepi alot

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: blood tests
Aktuelle Erkrankungen: -
Vorgeschichte: diabetes, afib, psorosis,
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: Moderna

VAERS 1917040

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 76,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 17.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 7,0
Dosis: 3
Route/Site: IM / LA

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

Chills Injection site infection Injection site scab Pain in extremity Pyrexia

Symptomtext

Patient described pain and soreness in upper arm one week after receiving injection as well as fever and chills. Used Neosporin on area. Doctor visit 11/23/2021: Injection site has small scab. Noticed infection without any surrounding erythema. Mildly tender to palpation. Rest of arm exam unremarkable with good range of motion.

Weitere VAERSDATA-Felder

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

VAERS 1915769

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NJ
Alter: 59,0
Geschlecht: F
Eingang: 02.12.2021
Impfdatum: 17.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Back pain

Symptomtext

This spontaneous case was reported by a pharmacist and describes the occurrence of BACK PAIN (severe backpain) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 17-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced BACK PAIN (severe backpain). At the time of the report, BACK PAIN (severe backpain) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered BACK PAIN (severe backpain) to be possibly related. No concomitant medication reported. No treatment information was provided. Patient was having severe backpain and the doctor said it's from the vaccine

Weitere VAERSDATA-Felder

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

VAERS 1912958

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 39,0
Geschlecht: F
Eingang: 01.12.2021
Impfdatum: 04.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / LA

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

Blood test normal Pruritus

Symptomtext

I had no immediate reactions. Starting on 11/14/2021 I developed skin itchiness in my hands, palms, feet, chest, and back. It was itchiness that was deep in the skin, so I didn't feel relief after itching. I went to the doctor and was told to stop taking my Lexapro and Prozac medications. I went to an urgent care and had blood work did. I don't have a diagnosis yet. I am going to see my PCP and possibly an allergist as well. I have been taking Benadryl and Zyrtec on and off which has been helping with the itching. I am feeling a little bit better now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: Bloodwork- normal (11/29/2021)
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Lexapro 10mg 1xday Prozac 10mg 1xday Prenatal Vitamin Prenatal Supplement Choline Tretinoin Clindamycin
Allergien: None
Vorherige Impfungen: COVID-19 Vaccine (2nd Dose)- I had a very sore arm, very tired, 103 fever, chills, and a headache. I had also developed a bumpy

VAERS 1910851

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 61,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Fatigue Gait disturbance Lymph node pain Lymphadenopathy Myalgia Oxygen saturation decreased Pyrexia Rectal haemorrhage Vaginal haemorrhage

Symptomtext

Fever for 3 days over 100 F. Treatment: OTC acetaminophen Muscle pains. Treatment: OTC acetaminophen Lymph nodes pains and swelling Low oxygen saturation (89) Severe fatigue Couldn?t walk unassisted Rectal and vaginal bleeding 3 days after injection

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Mitral stenosis Thyroid hormone deficiency
Andere Medikamente: Synthroid 88 mcg
Allergien: None
Vorherige Impfungen: Similar effects from 1st and second shot of Moderna Covid vaccine; lasting 9-10 days; March, April 2021; second shot side effect

VAERS 1909722

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NC
Alter: 60,0
Geschlecht: M
Eingang: 30.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Headache Pyrexia SARS-CoV-2 test Vaccine positive rechallenge

Symptomtext

Fevers up to 101.6 every day from the first shot on 10/11/2021 until 2 days before the second shot on 11/8/2021 Fevers started again on 11/8/2021 and continue through today, 11/30/2021. Headaches up to 101.6 every day from the first shot on 10/11/2021 until 2 days before the second shot on 11/8/2021 headaches started again on 11/8/2021 and continue through today, 11/30/2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: Dr requested COVID PCR test after two weeks of fevers
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Meloxicam, one-a-day, glucosimine
Allergien: None
Vorherige Impfungen: Fevers up to 101.6 every day from the first shot on 10/11/2021 until 2 days before the second shot on 11/8/2021 Fevers started a

VAERS 1909657

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NY
Alter: 29,0
Geschlecht: F
Eingang: 30.11.2021
Impfdatum: 29.11.2021
Beginn: 29.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Chills Dizziness

Symptomtext

Patient. received booster dose of Covid-19 Moderna Vaccine at 2:30pm, The Patient was walked to observation area. At 2:35pm she complained of dizziness and light headedness, patient provided with a chair to prop legs on and given 4 cups of cold water. Patient continued to complain of lightheadedness followed by chills. She was moved closer to heater vent in room. Vital signs obtained at 2:50pm blood pressure - 156/91, heart rate - 110,bpm pule oxygenation - 99% on room air. Patient was asked multiple times if she?s experiencing any shortness of breath or trouble breathing, nausea, vomiting, but continues to deny this throughout stay in observation area. RN in observation area recommended we call 911, but patient refused. Repeat Vital signs obtained again at 3:50p,m, and are as follows Blood Pressure 140/88, Heart rate 98BPM, Pulse oxygenation 99% on room air. Patient refused again transfer to hospital via EMS and does not want 911 called. Patient stated, she is willing to go to hospital and stated that she would prefer to have her friend take her. Patient's friend arrived at 4:15pm and they are escorted to vehicle out front door in stable condition with a RN. Patient's information collected for follow up. RN followed up on 11/30/21 at 8:50am. Patient stated she is feeling better and is not experiencing any shortness of breath, chills, fever or lightheaded ness. She is at home at the time of the follow up.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: patient denies
Vorgeschichte: patient denies
Andere Medikamente: patient denies
Allergien: patient denies
Vorherige Impfungen: -

VAERS 1906282

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MO
Alter: 36,0
Geschlecht: M
Eingang: 29.11.2021
Impfdatum: 01.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Dizziness Ear disorder Labyrinthitis Magnetic resonance imaging VIIIth nerve injury Vertigo Vomiting

Symptomtext

Diagnosed with vestibular labyrinthitis and otolith dysfunction (100%) to the right ear with permanent damage to the vestibular nerve. Sudden onset of severe vertigo began approximately 60 hours after administration of shot. Vertigo caused vomiting. More than three weeks later, there are lingering symptoms of dizziness. I have been undergoing vestibular therapy 3 times weekly, and am beginning to imporve.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: MRI, Vestibular analysis, hearing test.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Over-the-counter only: Zyrtec, Flonase, Famotidine
Allergien: Penicillin
Vorherige Impfungen: -

VAERS 1905951

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 57,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Fatigue Injection site pain Injection site pruritus Injection site rash Oropharyngeal pain Pain Pain in extremity Pyrexia Rhinorrhoea Upper-airway cough syndrome

Symptomtext

Pain in upper left arm began within minutes after injection. Fever (up to 102.5), chills, exhaustion, and body aches began 15 hours after injection. These symptoms occurred with my first two doses of Moderna and lasted for three days (the arm pain lasted for one week). In addition, the booster shot also gave me a runny nose, post-nasal drip, sore throat, and "Covid arm." The rash on my left arm was incredibly itchy and painful. It extended from the top of my shoulder to a couple of inches above my elbow, and has lasted four weeks. I used betamethasone cream to treat the allergic reaction and Sarna lotion to help with the itching. As of today, there are still some remnants of the rash, although the itching is controlled with Sarna lotion alone.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: No.
Aktuelle Erkrankungen: None
Vorgeschichte: Pre-diabetic, tendonitis in hands, acid reflux
Andere Medikamente: None
Allergien: Food: Tomatoes, potatoes (white varieties), peppers, eggplant, one type of yellow dye
Vorherige Impfungen: -

VAERS 1905511

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21a

mild

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 05.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Pain in extremity

Symptomtext

About 3 days after vaccines I experienced pain in right hand between thumb and forefinger. Fourth day after vaccine started experiencing joint pain in left hip and left knee. 23 days later, Nov 29, I still have both in both areas.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None yet.
Aktuelle Erkrankungen: None
Vorgeschichte: Diabetes T2 Asthma Hypertension
Andere Medikamente: Metformin 750mg Glipizide 2.5mg Aspirin 81mg Lisinopril 5mg Simvastatin 20mg
Allergien: None
Vorherige Impfungen: -

VAERS 1905506

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: OH
Alter: 69,0
Geschlecht: F
Eingang: 29.11.2021
Impfdatum: 05.11.2021
Beginn: 24.11.2021
Tage bis Beginn: 19,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Extra dose administered Joint swelling Pain in extremity Peripheral swelling

Symptomtext

On days 19,20,21 post Moderna booster, pain and joint swelling systemically but in particular in hands. Literally unable to use right hand at all due to extreme pain and joint swelling of entire hand. Abated over the course of several days with the use of Advil. No history of any arthritis at all prior to booster. Immediately post booster, also had 3 days of systemic and severe joint pain which then resolved, only to return again about 3 weeks later as noted above. Better now but not totally back to baseline normal.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None. Physician husband who confirmed adverse event. Also witnessed by numerous family members home for the holidays.
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: penicillin
Vorherige Impfungen: -

VAERS 1904387

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: SC
Alter: 95,0
Geschlecht: M
Eingang: 28.11.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / AR

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

Abdominal pain upper Back pain Blood pressure increased Chest X-ray Gastrointestinal wall thickening Scan abdomen abnormal Vomiting

Symptomtext

Dad was fine until 7:30 11/20/21. Called me to say he had terrible stomach pain, blood pressure through the roof. He vomited 2x. Neighbor had him call for an ambulance and rushed to emergency. when I arrived his BP was still very high and his pain was still bad. He remained in emergency until Sunday when a bed became available.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain upper
Hospital-Tage: 2,0
Labordaten: 11/21/21 had abdominal scan and chest xray. Thickening of small intestine and possible pneumonia. Pain was now in back and stomach.
Aktuelle Erkrankungen: He received a bag of blood a week before his vaccine . This was for his platelet issue.
Vorgeschichte: MDS, also stroke 2 years ago.
Andere Medikamente: Angrelide, eliquis, Tylenol, blood pressure med. I can't remember the exact one. Multivitamin plus K2, Areds (eye vitamin), B12, D3 CoQ10.
Allergien: ue.that I know of.
Vorherige Impfungen: -

VAERS 1904344

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MO
Alter: 44,0
Geschlecht: M
Eingang: 28.11.2021
Impfdatum: 26.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Fatigue Headache Injection site pain Injection site swelling

Symptomtext

Swelling and pain at injection site lasting at least 36 hrs, severe fatigue and headaches. Treated with 600mg of motrin every 6 hrs.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: allergies, high lipids
Andere Medikamente: Vascepa, lipitor, celexa, metformin, vitamin D, Coq10, Calcium
Allergien: Zinc Oxide, V-Cillin-K
Vorherige Impfungen: Similar reaction to dose 2 of Moderna Covid-19

VAERS 1904244

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NC
Alter: 49,0
Geschlecht: M
Eingang: 28.11.2021
Impfdatum: 27.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Chills Pain Pain in extremity Pyrexia

Symptomtext

Body aches, chills, fever, rt arm pain

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Htn, gerd, Barrett?s esophagus, depression
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: After second one. Same symptoms

VAERS 1903916

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MI
Alter: 33,0
Geschlecht: F
Eingang: 27.11.2021
Impfdatum: 15.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 8,0
Dosis: 1
Route/Site: SYR / LA

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

Rash macular Rash papular Skin swelling

Symptomtext

On day 8 after receiving the vaccine, a red swollen spot appeared, similar to how a mosquito bite looks, but there were two close together, about the size of a quarter. A few hours later, another appeared farther up my arm. These spread to the point of connecting and a third spot appeared, farther up my arm. These spread together, too. It has continued to grow, up my arm/shoulder. The edges are red and swollen like a ridge. It?s now (5 days of spreading) an oval shape measuring 3.5 inches by 2.5 inches. Ice on it made the puffiness subside for a few hours, but didn?t stop the spread. Tea tree essential oil (for hives) did nothing. Benedryl before bed didn?t do anything by morning either.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash macular
Hospital-Tage: -
Labordaten: None - I called the pharmacy and my primary care office. Both said to ?keep an eye on it.? If it?s still here by Monday (7 days after starting), I will go to the doctor?s office.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Children?s daily multivitamin
Allergien: None known
Vorherige Impfungen: -

VAERS 1902222

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: IL
Alter: 30,0
Geschlecht: F
Eingang: 26.11.2021
Impfdatum: 19.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Burning sensation Lip pruritus Periorbital swelling Pruritus Pyrexia Swelling face Urticaria

Symptomtext

On the morning following the Moderna Covid Booster Vaccination, my palms and upper lip became very itchy. The next morning, my right eyebrow was puffy and swollen, and hives appeared on my chest and neck. The hives appear and disappear randomly on my body. When they appear, the hives are itchy, feverish, and burning. They last about thirty minutes to forty-five minutes wherever they appear. After that time, they disappear from that spot on my body and appear somewhere else on my body. This happens day and night and has been going on since the morning after having received the booster shot.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Lip pruritus
Hospital-Tage: -
Labordaten: I went to a local health clinic on November 22nd. The Nurse Practitioner saw the hives and prescribed a Prednisone taper to help ease the intensity of the hives.
Aktuelle Erkrankungen: Sinus infection and strep throat.
Vorgeschichte: Seasonal allergies.
Andere Medikamente: Flonase, Allegra D, Pantoprazole, Cefuroxime.
Allergien: No known allergies to medications, food, or other products.
Vorherige Impfungen: -

VAERS 1901865

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CT
Alter: 59,0
Geschlecht: M
Eingang: 26.11.2021
Impfdatum: 22.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Pain in extremity Peripheral swelling

Symptomtext

Patient called pharmacy on Friday morning . He stated that his whole arm is red , swollen and hurts him. It started Tuesday and continued till Friday morning. Patient states he is stable and concerned about his arm.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: n/a
Allergien: n/a
Vorherige Impfungen: -

VAERS 1901680

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CT
Alter: 74,0
Geschlecht: F
Eingang: 26.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: OT / LA

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

Muscle swelling Oedema Pain in extremity Peripheral swelling Spider vein

Symptomtext

spider veins; legs ankles, calves swelled up/ swollen like balloons; edema; muscles swelled up; slight pain in her left arm; This spontaneous case was reported by a pharmacist and describes the occurrence of SPIDER VEIN (spider veins), PAIN IN EXTREMITY (slight pain in her left arm), PERIPHERAL SWELLING (legs ankles, calves swelled up/ swollen like balloons), OEDEMA (edema) and MUSCLE SWELLING (muscles swelled up) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 06-Nov-2021, the patient experienced PAIN IN EXTREMITY (slight pain in her left arm). On 09-Nov-2021, the patient experienced PERIPHERAL SWELLING (legs ankles, calves swelled up/ swollen like balloons), OEDEMA (edema) and MUSCLE SWELLING (muscles swelled up). On 12-Nov-2021, the patient experienced SPIDER VEIN (spider veins). On 09-Nov-2021, PAIN IN EXTREMITY (slight pain in her left arm) had resolved. On 12-Nov-2021, PERIPHERAL SWELLING (legs ankles, calves swelled up/ swollen like balloons), OEDEMA (edema) and MUSCLE SWELLING (muscles swelled up) had resolved. At the time of the report, SPIDER VEIN (spider veins) had not resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications was reported. Patient has not taken any medications or treatments for her symptoms.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pain in extremity
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1899598

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: SC
Alter: 78,0
Geschlecht: M
Eingang: 25.11.2021
Impfdatum: 15.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / LA

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

Headache Pain in extremity

Symptomtext

Little sore arm left arm injection; headache; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (Little sore arm left arm injection) and HEADACHE (headache) in a 78-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No medical history was provided by the reporter. On 15-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PAIN IN EXTREMITY (Little sore arm left arm injection) and HEADACHE (headache). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) for Headache, at an unspecified dose and frequency. At the time of the report, PAIN IN EXTREMITY (Little sore arm left arm injection) and HEADACHE (headache) outcome was unknown. No concomitant medication was provided. Husband called to report that he had a little sore arm left arm injection and a headache. Reports his wife has had swelling, hardness and redness at left arm injection site since receiving booster dose. States his wife had a headache all day yesterday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: No medical history was provided by the reporter.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1899519

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 27,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 01.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / LA

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

Injection site rash Rash Urticaria

Symptomtext

Delayed urticaria- began 10 days after vaccination. Is ongoing. Rashes and hives on moving spots all over the body. Also had "COVID arm" beginning the day after vaccination and lasting a few days-- rash around injection site.

Weitere VAERSDATA-Felder

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

VAERS 1899471

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: SC
Alter: 67,0
Geschlecht: F
Eingang: 25.11.2021
Impfdatum: 15.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / LA

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

Headache Vaccination site erythema Vaccination site induration Vaccination site swelling

Symptomtext

Swelling, hardness and redness at left arm injection site; Had a headache all day yesterday; Redness at left arm injection site; Hardness at left arm injection site; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE SWELLING (Swelling, hardness and redness at left arm injection site), HEADACHE (Had a headache all day yesterday), VACCINATION SITE ERYTHEMA (Redness at left arm injection site) and VACCINATION SITE INDURATION (Hardness at left arm injection site) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced VACCINATION SITE SWELLING (Swelling, hardness and redness at left arm injection site), HEADACHE (Had a headache all day yesterday), VACCINATION SITE ERYTHEMA (Redness at left arm injection site) and VACCINATION SITE INDURATION (Hardness at left arm injection site). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) for Headache, at an unspecified dose and frequency. At the time of the report, VACCINATION SITE SWELLING (Swelling, hardness and redness at left arm injection site), HEADACHE (Had a headache all day yesterday), VACCINATION SITE ERYTHEMA (Redness at left arm injection site) and VACCINATION SITE INDURATION (Hardness at left arm injection site) outcome was unknown. Concomitant medications were not reported. Treatment details were not provided.

Weitere VAERSDATA-Felder

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

VAERS 1897977

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: OH
Alter: 36,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Extra dose administered Pain Pyrexia

Symptomtext

Vaccine administration error: Patient stated they had not received a previous dose of any covid vaccine and was administered a full dose (0.5ml) instead of the half dose(0.25ml) for the third dose in the series. Vaccine was given at proper interval for booster dose >6 months after 2nd dose which was given on (04/21/21). At time of follow-up(11/23/21) patient reported normal side effects (fevers, chills, aches) that started approximately 8 hours post vaccination and had not fully resolved at that time.

Weitere VAERSDATA-Felder

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

VAERS 1897680

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MO
Alter: 77,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Erythema Pruritus Rash erythematous

Symptomtext

Red rash with bumps, itching, red, size: 9cm x 5cm

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma, Fibromyalgia
Andere Medikamente: Paxil, Thyroxine, magnesium, potassium, calcium, B complex, Niacinamide, D3+K2, C, Guaifenisin, Melatonin, Potassium, Zinc, Kelp, Biotin
Allergien: Prednisone
Vorherige Impfungen: -

VAERS 1897395

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: CA
Alter: 72,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 08.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness Feeling abnormal Flushing Hyperhidrosis Injection site bruising Injection site erythema Injection site pain Injection site pruritus Injection site swelling Nausea

Symptomtext

Site: Bruising at Injection Site-Severe, Site: Itching at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe, Systemic: Dizziness / Lightheadness-Severe, Systemic: felt horrible-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Nausea-Severe

Weitere VAERSDATA-Felder

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

VAERS 1896647

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 24,0
Geschlecht: F
Eingang: 24.11.2021
Impfdatum: 15.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Chills Headache Myalgia Pyrexia Vaccination site pain

Symptomtext

This spontaneous case was reported by a consumer and describes the occurrence of PYREXIA (lower fever), CHILLS (chills), MYALGIA (body aches that come and go), VACCINATION SITE PAIN (sore arm since the injection) and HEADACHE (feel like maybe started getting a headache) in a 24-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. Previously administered products included for COVID-19 vaccination: covid 19 vaccine janssen on 06-Mar-2021.Past adverse reactions to the above products included No adverse event with covid 19 vaccine janssen. On 15-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PYREXIA (lower fever), CHILLS (chills), MYALGIA (body aches that come and go), VACCINATION SITE PAIN (sore arm since the injection) and HEADACHE (feel like maybe started getting a headache). At the time of the report, PYREXIA (lower fever), CHILLS (chills), VACCINATION SITE PAIN (sore arm since the injection) and HEADACHE (feel like maybe started getting a headache) had not resolved and MYALGIA (body aches that come and go) outcome was unknown. Patient experiencing some mild side effect.No concomitant medication details was reported.No treatment medication details was reported.

Weitere VAERSDATA-Felder

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

VAERS 1895539

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 39,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 06.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 13,0
Dosis: 3
Route/Site: IM / LA

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

Exposure during pregnancy Pruritus Rash erythematous Sleep disorder

Symptomtext

Itching that started in my right ankle at night. The following morning, my chest became very itchy. Throughout the day, more parts of my body became extremely/intensely itchy and I developed red plaques/rash on my trunk/under the breasts, on my back, on my shoulders/blades. I took 1 dose of Benadryl 25mg, which helped a lot, but then later at night, the itchiness came back. I called the on-call service for my doctor's office, and per the recommendation of the nurse, I applied hydrocortisone 1% cream to the affected areas. I had difficulty sleeping due to the itching, so I took Benadryl 25mg. By the morning, the itching/rash improved a lot. Later in the day, there was some mild itching that I treated with hydrocortisone. I am currently 4.5 months pregnant with an expected due date of May 4th 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: -
Vorgeschichte: Asthma
Andere Medikamente: Prenatal multi-vitamin daily Cetirizine 10mg daily Fluticasone 50mcg nasal spray, 1 spray in each nostril daily Vitamin D 2,000 units daily Breo 200/25 mcg 1 puff inhaled orally daily
Allergien: Fentanyl=itching
Vorherige Impfungen: -

VAERS 1894929

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 61,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Chills Cough Headache Myalgia Nasopharyngitis Nausea Pain Sinus operation

Symptomtext

Nausea, headache , body aches. Sat nite had shaking chills that lasted at least 30minutes. No treatment. To this day I still get ha,nausea,muscle joint aches. I think I have a cold now- sinuses draining,coughing body aches

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: Achy joints
Vorgeschichte: PTSD, COPD, HTN, chronic pain
Andere Medikamente: Zoloft, Wellbutrin, losartan, amilopine
Allergien: NKA
Vorherige Impfungen: -

VAERS 1894748

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 05.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 6,0
Dosis: 3
Route/Site: SYR / RA

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

Injection site erythema Injection site pruritus Injection site swelling Pyrexia Urticaria

Symptomtext

I received the Moderna booster on 11/5. on 11/11, six days after receiving the Moderna booster shot, I developed an itchy bump at the injection site with red hives surrounding, it was feverish to the touch. Over the course next nearly two weeks, the hives have grown progressively worse, and are covering my entire body. I received a prednisone shot on 11/17, which only helped temporarily. Have since been taking oral prednisone and Benadryl daily, both of which barely alleviate the symptoms. I saw my allergist today, 11/23, and was prescribed Zyrtec, Pepcid AC, more prednisone, and an epi pen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None yet. Will get blood work next week.
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: Lexapro 20mgs
Allergien: penicillin, amoxicillin, sulfa drugs, shell fish, molds, pollens, pet dander
Vorherige Impfungen: -

VAERS 1893435

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: PA
Alter: 49,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 19.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 4,0
Dosis: UNK
Route/Site: SYR / LA

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

Extra dose administered Pain Urinary tract infection

Symptomtext

I woke up in the night with a raging urinary tract infection. Pain level was 7 or 8 out of 10. The shot I got was a booster.

Weitere VAERSDATA-Felder

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

VAERS 1892930

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: -
Alter: 59,0
Geschlecht: M
Eingang: 23.11.2021
Impfdatum: 12.11.2021
Beginn: 01.11.2021
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Vaccination site pain

Symptomtext

Minor pain/soreness at IM injecti on (booster) site.; This spontaneous case was reported by an other health care professional and describes the occurrence of VACCINATION SITE PAIN (Minor pain/soreness at IM injecti on (booster) site.) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. Previously administered products included for COVID-19 vaccination: Pfi zer COVID-19 vaccine (1st dose LOT-EP7534) on 23-Mar-2021 and Pfi zer COVID-19 vaccine (2nd dose LOT-EW0151) on 13-Apr-2021. Past adverse reactions to the above products included No adverse event with Pfi zer COVID-19 vaccine and Pfi zer COVID-19 vaccine. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced VACCINATION SITE PAIN (Minor pain/soreness at IM injecti on (booster) site.). At the time of the report, VACCINATION SITE PAIN (Minor pain/soreness at IM injecti on (booster) site.) outcome was unknown. No concomitant medication were reported No treatment medication were reported Minor pain/soreness at IM injection on (booster) site. Reported no pain from previous 2 Pfi zer doses.

Weitere VAERSDATA-Felder

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

VAERS 1892772

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: FL
Alter: 52,0
Geschlecht: F
Eingang: 23.11.2021
Impfdatum: 15.04.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / LA

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

Chills Discharge Headache Myalgia Pyrexia

Symptomtext

there was a body fluid coming under her arm, on the left side of her chest, it was flapping around; Chills; body aches; Fever; Headache; This spontaneous case was reported by a consumer and describes the occurrence of DISCHARGE (there was a body fluid coming under her arm, on the left side of her chest, it was flapping around), CHILLS (Chills), MYALGIA (body aches), PYREXIA (Fever) and HEADACHE (Headache) in a 53-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Apr-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced DISCHARGE (there was a body fluid coming under her arm, on the left side of her chest, it was flapping around), CHILLS (Chills), MYALGIA (body aches), PYREXIA (Fever) and HEADACHE (Headache). At the time of the report, DISCHARGE (there was a body fluid coming under her arm, on the left side of her chest, it was flapping around), CHILLS (Chills), MYALGIA (body aches), PYREXIA (Fever) and HEADACHE (Headache) outcome was unknown. NO Concomitant medication was reported NO treatment medication was reported This case was linked to MOD-2021-385672 (Patient Link).

Weitere VAERSDATA-Felder

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

VAERS 1890236

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21 A

mild

Staat: IN
Alter: 60,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 20.11.2021
Beginn: 21.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Chills Fatigue Pain Pyrexia

Symptomtext

Fever (102) Chills Body ache Fatigue This all lasted from 4 or 4:30 pm on November 21 until 2 am on November 22

Weitere VAERSDATA-Felder

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

VAERS 1889858

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CT
Alter: 30,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 10.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / LA

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

Pruritus Urticaria

Symptomtext

I first had itchy hands and then it spread to my scalp, chest, forearms, back, stomach, chest, and inner ears. It started 10 days after my third moderns booster. I took Benadryl but symptoms returned after 4 hours of the Benadryl treatment. Every time the symptoms returned it had spread to more parts of my body. Itchiness was accompanied by hives. I went to minute clinic and was prescribed triamcinilone ointment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pruritus
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Sertraline - 150 mg per day
Allergien: None known
Vorherige Impfungen: Moderna- chills, aches, headache. Symptoms came about 12 hours after shot. And dissipated after 1 day.

VAERS 1889799

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: IN
Alter: 62,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 20.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Fatigue Injection site pain Joint range of motion decreased Pyrexia

Symptomtext

Very sore arm at site of injection after about 4 hours; hard to lift arm above shoulder level. Continued into day 2 with less severity on day 3 (mild soreness? ability to lift higher) Slight / low-grade fever (approx 2 degrees higher than normal on day 2) Fatigue, lack of energy on day 2 Side effects not as severe w/ Booster dose as with Dose 2

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: Bronchitis
Vorgeschichte: N/A
Andere Medikamente: Vitamin D, probiotics (Culturelle)
Allergien: Shrimp/lobster etc Nickle
Vorherige Impfungen: Similar adverse effects with moderna Dose 2

VAERS 1889664

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: IL
Alter: 46,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 19.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site pain Muscular weakness

Symptomtext

Sore arm at injection site. Muscle weakness for approximately 3 days, continually diminishing. Back to normal 72 hours later.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Vitamin D
Allergien: None
Vorherige Impfungen: Sore injection site and arm with both previous doses of Pfizer COVID-19 vaccines. Age 45. Dates 3/17 and 4/14/2021.

VAERS 1889507

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: IL
Alter: 73,0
Geschlecht: F
Eingang: 22.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Impaired driving ability Injection site pain Muscle spasms

Symptomtext

Moderna Booster Patient is reporting muscle spasms and they have effected her ability to drive. Patient is also reporting slight soreness @ injection site. Patient states that she didn't experience this with first 2 doses

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: High blood pressure meds Stomach meds RA Pain meds Vitamin D Perosemide (Potassium)
Allergien: NONE
Vorherige Impfungen: -

VAERS 1888596

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: OH
Alter: 57,0
Geschlecht: F
Eingang: 21.11.2021
Impfdatum: 18.11.2021
Beginn: 20.11.2021
Tage bis Beginn: 2,0
Dosis: UNK
Route/Site: IM / LA

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

Rash Urticaria

Symptomtext

hives and rashes on body, to ER, prescribed oral steroids and steroid ointment; only 2 day since symptoms started, may take time to go away

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: fibromyalgia, lung scarring from chronic bronchitis growing up, disc bulges throughout spine, depression
Andere Medikamente: Middle of friday morning, had horrible chills, and uncontrollable shaking, stopped with tylenol; on sat morning arms began itching and hives had started and on my legs; started steroid cream and benadryl; by sunday morning the rash and hive
Allergien: Macrobid, Diflucan
Vorherige Impfungen: -

VAERS 1888255

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: DC
Alter: 32,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 18.11.2021
Beginn: 18.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Chills Injection site bruising Injection site erythema Injection site pain Injection site swelling Pain Pyrexia

Symptomtext

Site: Bruising at Injection Site-Medium, Site: Pain at Injection Site-Medium, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Chills-Medium, Systemic: Fever-Mild

Weitere VAERSDATA-Felder

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

VAERS 1888041

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 59,0
Geschlecht: F
Eingang: 20.11.2021
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: SYR / LA

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

Dizziness Vertigo

Symptomtext

I received the Moderna BOOSTER on 11/2/21 at 7pm. The next morning I was experiencing severe dizziness... then about a week later I started also experiencing vertigo. It is ongoing.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: None
Vorgeschichte: Obesity
Andere Medikamente: none
Allergien: penicillin allergy
Vorherige Impfungen: -

VAERS 1885668

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 56,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 18.11.2021
Beginn: 19.11.2021
Tage bis Beginn: 1,0
Dosis: 2
Route/Site: IM / LA

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

Chills Cough Fatigue Influenza like illness Pyrexia

Symptomtext

Mild to moderate flu-like symptoms five hours after injection; relieved with OTC ibuprofen. Moderate flu-like symptoms new onset 26 hours after vaccine administration, not relieved by ibuprofen. Extreme fatigue, mild chills, mild fever, slight cough.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Prilosec (20mg) Advil (400 mg)
Allergien: Eggs, nuts, shellfish, melons
Vorherige Impfungen: -

VAERS 1885184

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: SC
Alter: 57,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 16.11.2021
Beginn: 17.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chills Cough Dizziness Fatigue Headache Pain

Symptomtext

Woke up the next day with fatigue, headache, cough, weakness, body ache and chills. Dizzy if move head quickly. Symptoms continue 3 days after vaccine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: -
Vorgeschichte: 20 year 1 pack a day smoker
Andere Medikamente: multivitamin, stradiol
Allergien: penicillen
Vorherige Impfungen: -

VAERS 1884990

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CT
Alter: 83,0
Geschlecht: F
Eingang: 19.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Amnesia Asthenia Fatigue Lethargy

Symptomtext

Systemic: Exhaustion / Lethargy-Severe, Systemic: Dementia symptoms loss track of time/places.-Severe, Systemic: Weakness-Severe

Weitere VAERSDATA-Felder

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

VAERS 1884077

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NJ
Alter: 69,0
Geschlecht: M
Eingang: 19.11.2021
Impfdatum: 08.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: OT / -

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

Arthralgia Gait disturbance

Symptomtext

Can hardly walk; Having left ankle pain; This spontaneous case was reported by a consumer and describes the occurrence of GAIT DISTURBANCE (Can hardly walk) and ARTHRALGIA (Having left ankle pain) in a 69-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 11-Nov-2021, the patient experienced GAIT DISTURBANCE (Can hardly walk) and ARTHRALGIA (Having left ankle pain). At the time of the report, GAIT DISTURBANCE (Can hardly walk) and ARTHRALGIA (Having left ankle pain) outcome was unknown. No concomitant and medication information provided. No treatment information provided.

Weitere VAERSDATA-Felder

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

VAERS 1881024

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: IN
Alter: 42,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 13.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal pain Chills Faeces discoloured Fatigue Feeling abnormal Headache Hot flush Influenza like illness Injection site pruritus Injection site reaction Pain Pyrexia Urticaria

Symptomtext

FULL FLU LIKE SYMPTOMS STARTING THE DAY AFTER VACCINATION; EXTREME FATIGUE, PERSISTENT BODY ACHES, CHILLS, FEVER, HOT FLASHES, HEADACHE. THOSE LASTED UNTIL THE NEXT MORNING. THE 2 DAYS FOLLOWING THAT, I HAD GREEN BOWEL MOVEMENTS AND ABDONIMAL CRAMPING. THERE IS A WELT AT MY INJECTION SITE AND HAS BEEN ITCHY. I DID NOT EXPERINCE THAT WITH MY 1ST 2 DOSES. NOW 5 DAYS AFTER THE INJECTION, I AM ONCE AGAIN FEELING EXTREME FATIGUE AND BODY ACHES. I HAVE NOT FELT LIKE "MYSELF" FOR 5 DAYS NOW

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: ASTHMA
Andere Medikamente: -
Allergien: PCN / SULFA
Vorherige Impfungen: -

VAERS 1879929

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 53,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: 15.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Chills Fatigue Headache Influenza like illness Injection site erythema Injection site induration Injection site mass Injection site pruritus Injection site swelling Injection site warmth Pain Pyrexia

Symptomtext

Flu-like symptoms started 31 hours after I received my booster shot of Moderna - body aches, fatige and exhaustion, headache, sever chills, low grade fever. The next morning the injection site in my right arm was a hard lump, swollen, hot, red, and slightly itchy. The discomfort is localized to about 3 inches diameter. The rest of my arm is fine. The flu symptoms have resolved 24 hours after they started, but he arm is still red and itchy and swollen at the vaccine injection site.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: N/a
Vorgeschichte: Menopause
Andere Medikamente: Estradiol
Allergien: N/a
Vorherige Impfungen: Moderna 2nd dose on 2/17/2021 causes sever flu symptoms for 30 hours. Severe chills, fever, aches, headache.

VAERS 1879895

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 18.11.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: OT / -

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

Fatigue Vaccination site pain

Symptomtext

Fatigue; General pain at site of injection; This spontaneous case was reported by a patient family member or friend and describes the occurrence of FATIGUE (Fatigue) and VACCINATION SITE PAIN (General pain at site of injection) in a 45-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced FATIGUE (Fatigue) and VACCINATION SITE PAIN (General pain at site of injection). At the time of the report, FATIGUE (Fatigue) and VACCINATION SITE PAIN (General pain at site of injection) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. No concomitant medication information was provided. No treatment medication were provided.

Weitere VAERSDATA-Felder

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

VAERS 1879894

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: -
Alter: 53,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: OT / -

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

Chills Fatigue Headache Myalgia Pyrexia Vaccination site pain

Symptomtext

Headache; Chills; fever; Fatigue; muscle pain; pain in the arm of injection site; This spontaneous case was reported by a consumer and describes the occurrence of HEADACHE (Headache), CHILLS (Chills), PYREXIA (fever), FATIGUE (Fatigue) and MYALGIA (muscle pain) in a 53-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced HEADACHE (Headache), CHILLS (Chills), PYREXIA (fever), FATIGUE (Fatigue), MYALGIA (muscle pain) and VACCINATION SITE PAIN (pain in the arm of injection site). At the time of the report, HEADACHE (Headache), CHILLS (Chills), PYREXIA (fever), FATIGUE (Fatigue), MYALGIA (muscle pain) and VACCINATION SITE PAIN (pain in the arm of injection site) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. Concomitant product use was not provided by the reporter. Treatment information was not provided by the reporter.

Weitere VAERSDATA-Felder

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

VAERS 1879330

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: PA
Alter: 47,0
Geschlecht: M
Eingang: 18.11.2021
Impfdatum: 05.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Head discomfort Headache Pyrexia

Symptomtext

A heavy head; Feverish; Headache; This spontaneous case was reported by a consumer and describes the occurrence of HEAD DISCOMFORT (A heavy head), PYREXIA (Feverish) and HEADACHE (Headache) in a 47-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. The patient's past medical history included Heart attack (light heart attack years ago) and Stent placement (a heart stent). Previously administered products included for Product used for unknown indication: AstraZeneca Covisheild on 20-Mar-2021 and AstraZeneca Covisheild on 04-May-2021. Past adverse reactions to the above products included No adverse event with AstraZeneca Covisheild and AstraZeneca Covisheild. Concurrent medical conditions included Type II diabetes mellitus. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced HEAD DISCOMFORT (A heavy head), PYREXIA (Feverish) and HEADACHE (Headache). At the time of the report, HEAD DISCOMFORT (A heavy head), PYREXIA (Feverish) and HEADACHE (Headache) had not resolved. It was reported that patient has been getting feverish with a heavy head and headache those go away after about 5 hours then come back after another 3 hours. No relevant concomitant medications was reported. Treatment information was not provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Type II diabetes mellitus
Vorgeschichte: Medical History/Concurrent Conditions: Heart attack (light heart attack years ago); Stent placement (a heart stent)
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1877136

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: FL
Alter: 73,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 10.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: IM / LA

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

Injection site streaking

Symptomtext

gold streak from injection site

Weitere VAERSDATA-Felder

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

VAERS 1876428

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: ME
Alter: 75,0
Geschlecht: F
Eingang: 17.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / -

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

Chills Erythema Pruritus

Symptomtext

"Covid Arm" post Covid Moderna Booster- persistent redness and itching with chills

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: UTI
Vorgeschichte: Psoriatic Arthritis and Recurring UTI'S
Andere Medikamente: Lisinopril -10, Hydrochlorothiazide - 25, Omeprazole -25
Allergien: Sulphur drugs
Vorherige Impfungen: -

VAERS 1874157

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 33,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Dizziness

Symptomtext

Patient complained of light headed and dizzy. She was giving water and laid down after 3 mins of drinking water in a seating position. The ems was called after 15 mins because the patient was still feeling dizzy when she sad down. After being checked by the ems and asked to stand when patient affirmed of feeling better, she refused to go to the hospital. She left the building walking on her own to the car. She affirmed that she felt fine.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: posterior capacardia syndrome
Andere Medikamente: duloxetine, elinest, ibuprofen
Allergien: neosporin
Vorherige Impfungen: -

VAERS 1873865

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: MO
Alter: 73,0
Geschlecht: F
Eingang: 16.11.2021
Impfdatum: 16.11.2021
Beginn: 16.11.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / LA

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

Dizziness Immunisation Underdose

Symptomtext

The pt came in for her first dose of moderna vaccine. I accidentally gave her a booster dose (0.25ml). I needed to give her the rest (another 0.25ml) During that time she was a little light-headed and needed to rest for a while. She did tell me that it was probably all in her head, but I kept checking in with her anyways. I gave her the rest of her dose and everything was fine. There were no rashes, hives, itching, SOB, or other issues. Water was given and rest.

Weitere VAERSDATA-Felder

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

VAERS 1871143

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 52,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 31.10.2021
Beginn: 01.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Cough Fatigue Illness Oropharyngeal pain Rhinorrhoea

Symptomtext

I was sick in bed for four days unable to get up except to occasionally use the rest room. I had no fever, but I did have a runny nose, cough, and sore throat which disappeared after I was able to get up on the fifth day. This was far worse than the one day of tiredness listed as a normal reaction.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Migraine headaches, fibromyalgia
Andere Medikamente: Lyrica, Zyrtec, vitamin B2, sucralfate, omeprazole, D3
Allergien: Compezine. Reglan
Vorherige Impfungen: -

VAERS 1870653

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: GA
Alter: 46,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / RA

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

Fatigue Headache Injection site pain Injection site reaction Injection site swelling Pain Rash erythematous

Symptomtext

Swelling, pain and red rash at the injection site. Felt achy, tired and had a headache for a day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Fatigue
Hospital-Tage: -
Labordaten: No
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Wellbutrin
Allergien: No
Vorherige Impfungen: Same aches and swelling & red rash at injection site. 1/28/2021 lot 028L20A Moderna 46 years

VAERS 1869983

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: VA
Alter: 78,0
Geschlecht: M
Eingang: 15.11.2021
Impfdatum: 11.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Chills Micturition urgency Pain Vaccination site pain

Symptomtext

Initial minor soreness at vaccination site. At 2:00 am, I experienced intense shivering, perspiration, body aches and the repeated need to urinate (about 10 or 12 times over the following two and a half hours). The symptoms were very similar to malaria (which I've had four times), although these symptoms, especially the shivering, seemed more intense (perhaps because of my advancing age). It got to the point where I was intent upon calling 911 if the symptoms didn't subside by 5:00 pm. But they subsided before then, and I went back to sleep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None.
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension, recovered from atrial fibrilation and prostate cancer
Andere Medikamente: Eliquis, Losartan, Amlodipine, Atorvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 1869470

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NJ
Alter: 73,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 09.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Extra dose administered Injection site rash

Symptomtext

Pt. states that after receiving the 3rd Booster of Moderna 11/09/2021, started experiencing symptoms 11/11/2021 of rash developed the left arm at the injection site spreading throughout to the elbow. No noted Primary visit/recommendations. Pharmacist communications recommendation for Cortisone Cream for self-treatment.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site rash
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/A
Andere Medikamente: N/A
Allergien: Shellfish
Vorherige Impfungen: -

VAERS 1869343

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: -
Alter: 53,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 12.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Injection site hypoaesthesia Injection site swelling Pyrexia

Symptomtext

JOINT PAIN, FEVER, SWELLING AT INJECTION SITE WITH NUMBNESS OF RIGHT ARM (ARM OF INJECTION)

Weitere VAERSDATA-Felder

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

VAERS 1869169

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: TN
Alter: 47,0
Geschlecht: F
Eingang: 15.11.2021
Impfdatum: 13.11.2021
Beginn: 14.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Lymphadenopathy Pyrexia

Symptomtext

Day2 fever and lymph node swelling in arm vaccine given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Cold 1weeks prior
Vorgeschichte: -
Andere Medikamente: Multi vitamins, fish oil , baby aspirin and. Multi symptom menopause medication. Equate brand
Allergien: -
Vorherige Impfungen: -

VAERS 1868211

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: MA
Alter: 65,0
Geschlecht: F
Eingang: 14.11.2021
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site erythema Injection site swelling Injection site warmth

Symptomtext

Site: Swelling at Injection Site-Mild, Additional Details: redness and warm to the touch below injection site and above elbow. resolved on its own improving each day.

Weitere VAERSDATA-Felder

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

VAERS 1867887

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: RI
Alter: 65,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Dysuria Fatigue Haematuria Micturition urgency Pain

Symptomtext

REceived shot at 9:30 am, symptoms started at 7:30 - severe fatigue, chills, ache, which continued till next day at 1:30 pm. Urgency with poor voiding started about 11:30 pm on day of vaccination, hematuria started next morning. Still continuing

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: Acetaminophen
Allergien: doxycycline
Vorherige Impfungen: -

VAERS 1867710

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NC
Alter: 41,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 01.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 4,0
Dosis: 1
Route/Site: SYR / LA

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

Rash erythematous

Symptomtext

Red rash on left arm, stomach, left hip and buttocks

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash erythematous
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Biotin, Vitamin D, Fish Oil, Magnesium, Probiotic and Prebiotics gummie
Allergien: None
Vorherige Impfungen: -

VAERS 1867480

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CA
Alter: 58,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 08.11.2021
Beginn: 12.11.2021
Tage bis Beginn: 4,0
Dosis: 2
Route/Site: SYR / LA

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

Arthralgia Neck pain Swelling

Symptomtext

Left neck/shoulder pain and swelling at left side of collarbone

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: No
Andere Medikamente: Levathyroxine Vitamins
Allergien: Penicillin, Levaquin, Monistat, cephalosporins, gabapentin, avocado, blue cheese
Vorherige Impfungen: -

VAERS 1867168

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CT
Alter: 71,0
Geschlecht: F
Eingang: 13.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Bedridden Body temperature Decreased appetite Influenza like illness Myalgia Nausea Pyrexia

Symptomtext

flue like symptoms; No appetite; bed ridden for a whole day; Achy body; nauseous; Fever of 100.3; This spontaneous case was reported by a consumer and describes the occurrence of INFLUENZA LIKE ILLNESS (flue like symptoms), DECREASED APPETITE (No appetite), BEDRIDDEN (bed ridden for a whole day), MYALGIA (Achy body) and NAUSEA (nauseous) in a 71-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Cholesterol and Acid reflux (esophageal). Concomitant products included FAMOTIDINE for Acid reflux (esophageal), ROSUVASTATIN for Cholesterol, METOPROLOL for an unknown indication. On 04-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Nov-2021, the patient experienced INFLUENZA LIKE ILLNESS (flue like symptoms), DECREASED APPETITE (No appetite), BEDRIDDEN (bed ridden for a whole day), MYALGIA (Achy body), NAUSEA (nauseous) and PYREXIA (Fever of 100.3). On 05-Nov-2021, PYREXIA (Fever of 100.3) had resolved. On 06-Nov-2021, BEDRIDDEN (bed ridden for a whole day) had resolved. At the time of the report, INFLUENZA LIKE ILLNESS (flue like symptoms), DECREASED APPETITE (No appetite), MYALGIA (Achy body) and NAUSEA (nauseous) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 04-Nov-2021, Body temperature: 100.3 (High) Body temperature High-100.3. Reporter stated that patient was taking concomitant medication metoprolol for betablocker, rosuvastatin for cholesterol control and famotidine for acid reflux. Treatment details was not reported by the reporter.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Myalgia
Hospital-Tage: -
Labordaten: Test Date: 20211104; Test Name: Body temperature; Result Unstructured Data: Body temperature High-100.3
Aktuelle Erkrankungen: Acid reflux (esophageal); Cholesterol
Vorgeschichte: -
Andere Medikamente: METOPROLOL; ROSUVASTATIN; FAMOTIDINE
Allergien: -
Vorherige Impfungen: -

VAERS 1865274

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NJ
Alter: 66,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 10.11.2021
Beginn: 11.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: SYR / -

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

Arthralgia Chills Fatigue Injection site pain Myalgia Nausea

Symptomtext

Nauseous Tired Joint pain Muscle pain Chills Pain at injection site Have all symptoms next day

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: IBS
Vorgeschichte: IBS
Andere Medikamente: Clonazepam Atorvastatin sertraline Famotidine
Allergien: Levofloxacin Latex Lactose intolerant
Vorherige Impfungen: -

VAERS 1864459

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 70,0
Geschlecht: F
Eingang: 12.11.2021
Impfdatum: 02.11.2021
Beginn: 03.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: OT / -

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

Dizziness Gait disturbance

Symptomtext

"woozy like on a boat and unsteady/ I walked into a walk heading into the bathroom"; woozy like on a boat and unsteady; This spontaneous case was reported by an other health care professional and describes the occurrence of GAIT DISTURBANCE ("woozy like on a boat and unsteady/ I walked into a walk heading into the bathroom") and DIZZINESS (woozy like on a boat and unsteady) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. Concurrent medical conditions included Peripheral neuropathy. Concomitant products included GABAPENTIN for Peripheral neuropathy, LEVOTHYROXINE and VENLAFAXINE HYDROCHLORIDE (EFFEXOR) for an unknown indication. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 03-Nov-2021, the patient experienced GAIT DISTURBANCE ("woozy like on a boat and unsteady/ I walked into a walk heading into the bathroom") and DIZZINESS (woozy like on a boat and unsteady). At the time of the report, GAIT DISTURBANCE ("woozy like on a boat and unsteady/ I walked into a walk heading into the bathroom") and DIZZINESS (woozy like on a boat and unsteady) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Patient took 1st dose on 01Feb2021 having lot number 028L20A and 2nd dose on 01Mar2021 having lot number 011A21A No treatment information were reported by the reporter

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Peripheral neuropathy
Vorgeschichte: -
Andere Medikamente: LEVOTHYROXINE; GABAPENTIN; EFFEXOR
Allergien: -
Vorherige Impfungen: -

VAERS 1863591

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: MA
Alter: 29,0
Geschlecht: M
Eingang: 12.11.2021
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Chills Headache Myalgia Pain in extremity Pyrexia

Symptomtext

arm soreness; arm soreness,body aches; headaches; 39?C fever; chills; This spontaneous case was reported by a consumer and describes the occurrence of PAIN IN EXTREMITY (arm soreness), MYALGIA (arm soreness,body aches), HEADACHE (headaches), PYREXIA (39?C fever) and CHILLS (chills) in a 29-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033f21a) for COVID-19 vaccination. Previously administered products included for an unreported indication: PFIZER BIONTECH COVID-19 VACCINE (lot# w0158) on 09-Apr-2021 and PFIZER BIONTECH COVID-19 VACCINE (lot# eu00171) on 26-Apr-2021. On 02-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-Nov-2021, the patient experienced PAIN IN EXTREMITY (arm soreness) and MYALGIA (arm soreness,body aches). 02-Nov-2021, the patient experienced HEADACHE (headaches), PYREXIA (39?C fever) and CHILLS (chills). At the time of the report, PAIN IN EXTREMITY (arm soreness), MYALGIA (arm soreness,body aches), HEADACHE (headaches), PYREXIA (39?C fever) and CHILLS (chills) outcome was unknown. No concomitant medication was reported. No treatment medication was reported.

Weitere VAERSDATA-Felder

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

VAERS 1861832

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CA
Alter: 73,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Headache Injection site erythema Injection site pruritus Injection site swelling Injection site warmth

Symptomtext

The day after my booster, the injection site swelled, got very red, hot, and itchy. It was circular...about 3 inches in diameter. I put Benadryl cream on it, and cortisone cream , iced a bit and took Zyrtec for the itching (which helped). Today, almost a week later from the reaction, it is much better. still a bit red, heat is gone. It might be a bit swollen, but not too visible .In the 2 previous shots this did not happen. only achy and tired and headache the 2nd time. had a headache this time too.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: High blood pressure, obesity
Andere Medikamente: Atorvastatin, baby aspirin, levothyroxine, hydrochlorothyazide. carvedilol, hydralazine, calcium and multivitamin
Allergien: penicillin possibly high
Vorherige Impfungen: face got red and hot . lasted about 10 minutes

VAERS 1861176

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MI
Alter: 81,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Asthenia Chills Diarrhoea Fatigue Injection site erythema Injection site pain Injection site swelling Lethargy Nausea Pain

Symptomtext

Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Chills-Mild, Systemic: Diarrhea-Medium, Systemic: Exhaustion/Lethargy-Medium, Systemic: Nausea-Medium, Systemic: Weakness-Medium.

Weitere VAERSDATA-Felder

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

VAERS 1860806

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: TX
Alter: 81,0
Geschlecht: F
Eingang: 11.11.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: SYR / LA

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

Chills Myalgia Nausea Pyrexia

Symptomtext

Sore body muscles throughout, for about 30 hours; slight nausea for about 30. Minutes, fever, chills.

Weitere VAERSDATA-Felder

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

VAERS 1858503

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CA
Alter: 66,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 09.11.2021
Beginn: 10.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Discomfort Headache Insomnia Nausea Pyrexia

Symptomtext

Fever, nausea, headache, discomfort, inability to sleep.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Headache
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Levothyroxine Atorvastatin
Allergien: None
Vorherige Impfungen: Moderna Covid-19

VAERS 1857607

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: IL
Alter: 85,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Injection site pruritus

Symptomtext

I developed itching at and around the injection in about 8 hours after the injection. The itching has continued but is better after three days but it has not stopped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site pruritus
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: non
Vorgeschichte: glaucoma and hypothyroidism.
Andere Medikamente: synyhroid, low dose aspirin, rosuvastain, multivitamin and travatan eye drops.
Allergien: sulfa drugs, some foods and some pain medications.
Vorherige Impfungen: -

VAERS 1857165

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: OH
Alter: 23,0
Geschlecht: F
Eingang: 10.11.2021
Impfdatum: 05.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Headache Rash

Symptomtext

Systemic: Allergic: Rash (specify: facial area, extremeties)-Medium, Systemic: Allergic: Rash Generalized-Medium, Systemic: Headache-Severe

Weitere VAERSDATA-Felder

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

VAERS 1855772

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NY
Alter: 42,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 06.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / RA

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

Abdominal pain Pyrexia

Symptomtext

Fever starting Sunday. Abdominal pain starting Monday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal pain
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: N/A
Vorgeschichte: Fibromyalgia Sickle cell Trait
Andere Medikamente: Zyrtec NAC Glucosamine
Allergien: NSAIDS Tree Nuts Sulfites
Vorherige Impfungen: -

VAERS 1854069

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: NJ
Alter: 39,0
Geschlecht: F
Eingang: 09.11.2021
Impfdatum: 06.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Extra dose administered Injection site erythema Injection site pruritus Injection site reaction Urticaria

Symptomtext

Between baseball and golfball size itchy red whelt at injection site still present 3 days after vaccine dose administered.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Injection site erythema
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Environmental Allergies
Andere Medikamente: Sudafed, Claritin
Allergien: Latex
Vorherige Impfungen: -

VAERS 1853722

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21a

mild

Staat: IL
Alter: 33,0
Geschlecht: M
Eingang: 09.11.2021
Impfdatum: 07.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Fatigue Feeling abnormal Joint stiffness Pain Pyrexia

Symptomtext

Fever, body aches, sore and stiff joints, brain fog, fatigue

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Depression
Andere Medikamente: Lexapro 20mg
Allergien: None
Vorherige Impfungen: -

VAERS 1850928

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: GA
Alter: 77,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 04.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Injection site bruising Injection site erythema Injection site pain Injection site pruritus Injection site swelling Pruritus

Symptomtext

Site: Bruising at Injection Site-Mild, Site: Itching at Injection Site-Mild, Site: Pain at Injection Site-Mild, Site: Redness at Injection Site-Mild, Site: Swelling at Injection Site-Mild, Systemic: Allergic: Itch Generalized-Mild

Weitere VAERSDATA-Felder

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

VAERS 1850753

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: TX
Alter: 34,0
Geschlecht: F
Eingang: 08.11.2021
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Chills Erythema Exposure during pregnancy Headache Pain in extremity

Symptomtext

I was 14 weeks pregnant when I got the shot. This was a booster (half dose) I had chills, arm soreness, covid arm (red patch), headache that was moderate/severe and only occurred momentarily when changing positions. The headache was the worst part. It has lasted until today (11/8) but is much better today and yesterday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: neurocardiogenic syncope
Andere Medikamente: prenatal vitamins
Allergien: latex
Vorherige Impfungen: -

VAERS 1849712

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21a

mild

Staat: CA
Alter: 47,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 05.11.2021
Beginn: 07.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Rash macular

Symptomtext

48 hours post inject a large red splotch appeared below injection site going down my arm. This did not happen with my first two injections

Weitere VAERSDATA-Felder

Praegender Schweregrund: Rash macular
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: No
Vorgeschichte: Migraines, bladder disease
Andere Medikamente: Imodium, Ativan, neurontin, Aimovig, combipatch, divergel
Allergien: Gluten
Vorherige Impfungen: -

VAERS 1849497

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: NY
Alter: 69,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / -

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

Chills Gastrointestinal disorder Hyperhidrosis Pyrexia

Symptomtext

Fever of 101. 2 Chills Sweats Stomach

Weitere VAERSDATA-Felder

Praegender Schweregrund: Chills
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: No
Allergien: No
Vorherige Impfungen: -

VAERS 1849244

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21A

mild

Staat: TX
Alter: 40,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 06.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / LA

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

Dizziness

Symptomtext

Systemic: Dizziness / Lightheadness-Medium, Additional Details: Vital signs were normal. Pt bp was 118/82 pulse was 64. Gave a picec of candy after vaccination and advised to wait. States she is feeling better

Weitere VAERSDATA-Felder

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

VAERS 1849239

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: OH
Alter: 74,0
Geschlecht: F
Eingang: 07.11.2021
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Arthralgia Blister Erythema Herpes zoster Musculoskeletal stiffness Pain in extremity Pruritus

Symptomtext

Nov 1, 2021 8 hours sore arm, L hip pain Nov 2 stiff arm, L hip pain severe feels like orthopedic concern Nov 3 hip pain severe Nov 4 red area on lower back Nov 5 red blisters, slight itching shingles suspected Nov 6 urgent care Shingles (056.9, B02.9) prescribed acyclovir 800 mg; prednisone 20 mg; gabapentin 300 mg Nov 7 multiple areas of blisters remain, hip pain has resolved

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NONE
Vorgeschichte: Hypertension Anxiety
Andere Medikamente: xanax atenolol spironolactone&HCTZ Restasis
Allergien: codeine
Vorherige Impfungen: -

VAERS 1848984

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CT
Alter: 53,0
Geschlecht: M
Eingang: 06.11.2021
Impfdatum: 05.11.2021
Beginn: 06.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Arthralgia Chest discomfort Fatigue Feeling jittery Headache Myalgia Somnolence

Symptomtext

Head ache equal to a migraine in severity Jittery woke up feeling as though I had too much caffeine or when I am nervous. Settled down by 1pm today Tightness in chest and lungs feels as if I've taken a deep breath on a really cold day. Been there since I woke this morning. Breathing is not hampered at all and remains normal. Very tired, feels like I could sleep all day. Tried to do normal activity and became tired quickly. Have been resting at home all day. No plans to leave house. Joint and muscle aches throughout the day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Arthralgia
Hospital-Tage: -
Labordaten: N/A
Aktuelle Erkrankungen: No
Vorgeschichte: No
Andere Medikamente: Tadalafil 5mg Tablet by mouth daily Bupropion 450mg by mouth daily Simvastatin 40mg 1 tablet nightly Propranolol 10MG tablet 2 tablets daily Clonazepam 1mg 2 tablets daily
Allergien: Leviquin
Vorherige Impfungen: -

VAERS 1848919

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: PA
Alter: 63,0
Geschlecht: F
Eingang: 06.11.2021
Impfdatum: 03.11.2021
Beginn: 05.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: - / LA

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

Fatigue Injection site erythema Injection site mass Injection site pruritus

Symptomtext

The patient had extreme tiredness for 2 days post vaccination and her arm around the injection site became red and itching with a large white lump at injection site that is still present as of today (3 days post vaccine).

Weitere VAERSDATA-Felder

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

VAERS 1846986

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: AZ
Alter: 62,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 31.10.2021
Beginn: 03.11.2021
Tage bis Beginn: 3,0
Dosis: 3
Route/Site: SYR / RA

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

Dizziness Extra dose administered Gait disturbance Vertigo

Symptomtext

Dizziness and Vertigo started on Thursday late afternoon 11/4 and worsened throughout the day. Staggering when walking on 11/5. Shot given on 10/31.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dizziness
Hospital-Tage: -
Labordaten: N/a
Aktuelle Erkrankungen: Sinusitus
Vorgeschichte: Celiac Disease, Lichens Schelrosis, Asthma, Aortic Stenosis
Andere Medikamente: Cyclobenzaprine.
Allergien: Celiac (wheat gluten), Celclor, Augmenten, Bactrim, Cipro
Vorherige Impfungen: -

VAERS 1846942

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 26,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 03.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Interchange of vaccine products Nausea Pyrexia Vomiting

Symptomtext

I received the Johnson and Johnson vaccine April 6th 2021. I received my moderna booster at 6:45pm. By 2am I was extremely nauseous and vomiting until 8am. My fever of 102 started around 8am, I needed to take Zofran in order to keep my Tylenol down. My fever with Tylenol 1000mg every 6 hours stayed around 101.5 until 48 hours after my vaccine. It is now 48 hours after my vaccine and I still have a 101.5 fever.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Nausea
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Exercise induced asthma, anxiety
Andere Medikamente: Mirena IUD, Apri oral birth control
Allergien: Nond
Vorherige Impfungen: -

VAERS 1846711

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: MA
Alter: 75,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 04.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Injection site pain Pyrexia

Symptomtext

Site: Pain at Injection Site-Mild, Systemic: Fever-Severe

Weitere VAERSDATA-Felder

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

VAERS 1846565

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CT
Alter: 36,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 29.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 2,0
Dosis: N/A
Route/Site: IM / LA

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

Interchange of vaccine products Pyrexia Rash Rash erythematous Rash morbilliform Rash papular Rash pruritic Urticaria

Symptomtext

This was a booster shot of Moderna COVID vaccine. I had J&J for my original vaccine in April 2020. Booster received 10/29/21 at 5:45pm, mild fever from 10/30-10/31/21. Upon waking on 11/01/21 I had a measles-like rash on my back and chest, which rapidly turned into hives and spread to my scalp and face by 7pm on 11/01/21. It is extremely itchy, raised, and red. I took 50 mg of benadry on 11/01/21 and 11/02/21 which did not resolve any symptoms. I saw an APN on 11/03/21 who prescribed a course of prednisone that I began that day. As of 11/05/21 I still have the full rash and hives, which have barely improved.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Pyrexia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: NA
Vorgeschichte: endometriosis, adenomyosis
Andere Medikamente: loratadine 10mg, vitamin D 2000IU, emotional wellness, rhodiola rosa, Kava extract, magnesium buffered chelate, CBD 25mg
Allergien: sulfa drugs
Vorherige Impfungen: -

VAERS 1845974

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: MA
Alter: 52,0
Geschlecht: M
Eingang: 05.11.2021
Impfdatum: 02.11.2021
Beginn: 04.11.2021
Tage bis Beginn: 2,0
Dosis: 1
Route/Site: IM / LA

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

Pain in extremity Peripheral swelling Tenderness

Symptomtext

Swelling under left arm, pain & tenderness.

Weitere VAERSDATA-Felder

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

VAERS 1845908

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

mild

Staat: CA
Alter: 52,0
Geschlecht: F
Eingang: 05.11.2021
Impfdatum: 29.10.2021
Beginn: 29.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Confusional state Fatigue Headache Injection site pain Lethargy Lymphadenopathy Pain

Symptomtext

Site: Pain at Injection Site-Medium, Systemic: Body Aches Generalized-Medium, Systemic: Confusion-Medium, Systemic: Exhaustion / Lethargy-Medium, Systemic: Headache-Medium, Systemic: Lymph Node Swelling-Medium, Additional Details: lymph node swelling was in left armpit

Weitere VAERSDATA-Felder

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

VAERS 1842776

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: OH
Alter: 50,0
Geschlecht: F
Eingang: 04.11.2021
Impfdatum: 30.10.2021
Beginn: 30.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Injection site bruising Injection site erythema Injection site pain Injection site pruritus Injection site swelling

Symptomtext

Site: Bruising at Injection Site-Severe, Site: Itching at Injection Site-Severe, Site: Pain at Injection Site-Severe, Site: Redness at Injection Site-Severe, Site: Swelling at Injection Site-Severe

Weitere VAERSDATA-Felder

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

VAERS 1837385

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

mild

Staat: CA
Alter: 77,0
Geschlecht: F
Eingang: 02.11.2021
Impfdatum: 31.10.2021
Beginn: 31.10.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Diarrhoea Headache Insomnia Nausea Pyrexia Vomiting

Symptomtext

Sunday: Big headache, unable to sleep soundly, nausea. Monday: fever (102.1, no Tylenol yet), and eventual vomiting and diarrhea on the next day, morning and afternoon. Symptoms had mostly subsided by midnight on Monday.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Diarrhoea
Hospital-Tage: -
Labordaten: Went to ER on Monday 11/1 evening when diarrhea subsided enough to travel. Observed there for 5 or 6 hours, when fever no longer high, all vitals monitored
Aktuelle Erkrankungen: nothing
Vorgeschichte: minimal
Andere Medikamente: Vitamin D 400 IU
Allergien: traditional nasal allergies, minimal in my old age
Vorherige Impfungen: -

VAERS 2653131

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 87,0
Geschlecht: M
Eingang: 06.07.2023
Impfdatum: 03.11.2021
Beginn: 03.02.2022
Tage bis Beginn: 92,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Moderna 2/11/21 lot# 015M20A; Moderna 3/11/21 lot# 044A21A; Moderna 11/3/21 lot# 033F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2652804

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MA
Alter: 26,0
Geschlecht: M
Eingang: 05.07.2023
Impfdatum: 07.11.2021
Beginn: 24.04.2022
Tage bis Beginn: 168,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Cough Rhinorrhoea SARS-CoV-2 test positive

Symptomtext

On about 4/24/2022, I developed a cough and runny nose. I took a home antigen test on 4/25/2022 and got a positive result. On 4/26/2023, I went to a clinic at a pharmacy and underwent a rapid test, which confirmed the positive result of the home test. I was prescribed Paxlovid, which I began taking 4/26/2022. The medication left a nasty, metallic aftertaste in my mouth, but aside from that, I had no other side effects. Within 24 hours of beginning the Paxlovid, I began to feel better. I finished the five-day course of Paxlovid, and I tested negative on 5/6/2022. I followed the CDC protocols for self-isolation during this time. On 6/13/2022, I had a cough and runny nose, At 3:46 PM on that day, I took a home antigen test and got a positive result. I called my NP and had a telehealth visit with him. Because of the timing of the illness, I asked him if it could be a rebound case. He didn't think it was a rebound, but he also decided not to prescribe me Paxlovid, because at that time, there was no guidance regarding prescribing it so soon after having already prescribed it. At this time, there was a new omicron subvariant of COVID-19, and my NP thought that this may have been the reason why I caught COVID-19 again so quickly after having gotten it the first time. However, he didn't run any tests to determine the strain that I had. Again, I followed the CDC protocols for self-isolation, and I felt better a few days after the onset of symptoms. On 6/23/2022, I took a home antigen test and got a negative result.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 25APR2022 - Home Antigen Test - Positive Result; 26APR2022 - Clinical Rapid Antigen Test - Positive Result; 06MAY2022 - Home Antigen Test - Negative Result; 13JUN2022 - Home Antigen Test - Positive Result; 23JUN2022 - Home Antigen Test - Negative Result
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Emtricitabine / Tenofovir
Allergien: None
Vorherige Impfungen: -

VAERS 2647968

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 48,0
Geschlecht: F
Eingang: 21.06.2023
Impfdatum: 19.11.2021
Beginn: 03.06.2022
Tage bis Beginn: 196,0
Dosis: 3
Route/Site: IM / AR

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

On 6/3/2022, I underwent a PCR test and got a positive result. I did not develop any symptoms of COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 03JUN2022 - PCR Test - Positive Result
Aktuelle Erkrankungen: None
Vorgeschichte: Hypertension; High Cholesterol; Depression; Anxiety
Andere Medikamente: Prozac; Lisinopril; Atorvastatin
Allergien: None
Vorherige Impfungen: -

VAERS 2647330

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 72,0
Geschlecht: M
Eingang: 20.06.2023
Impfdatum: 13.11.2021
Beginn: 11.06.2023
Tage bis Beginn: 575,0
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# 030A21A; Moderna 4/6/21 lot# 017B21A; Moderna 11/13/21 lot# 033F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2636186

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: 64,0
Geschlecht: M
Eingang: 24.05.2023
Impfdatum: 04.11.2021
Beginn: 23.12.2021
Tage bis Beginn: 49,0
Dosis: 3
Route/Site: - / -

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

Obstructive sleep apnoea syndrome

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE OBSTRUCTIVE SLEEP APNEA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Obstructive sleep apnoea syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2636079

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: 67,0
Geschlecht: F
Eingang: 24.05.2023
Impfdatum: 27.12.2021
Beginn: 09.04.2022
Tage bis Beginn: 103,0
Dosis: 3
Route/Site: IM / LA

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

Obstructive sleep apnoea syndrome

Symptomtext

OBSTRUCTIVE SLEEP APNEA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Obstructive sleep apnoea syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2629788

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 61,0
Geschlecht: M
Eingang: 10.05.2023
Impfdatum: 17.11.2021
Beginn: 15.01.2022
Tage bis Beginn: 59,0
Dosis: 2
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 2 vaccines Moderna 10/0/21 Lot# 061E; Moderna 11/17/21 Lot# 033F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2629784

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: 46,0
Geschlecht: M
Eingang: 10.05.2023
Impfdatum: 30.11.2021
Beginn: 02.12.2022
Tage bis Beginn: 367,0
Dosis: 3
Route/Site: IM / LA

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

Obstructive sleep apnoea syndrome

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE ADULT OBSTRUCTIVE SLEEP APNEA, MODERATE

Weitere VAERSDATA-Felder

Praegender Schweregrund: Obstructive sleep apnoea syndrome
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2628303

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: 60,0
Geschlecht: F
Eingang: 08.05.2023
Impfdatum: 30.11.2021
Beginn: 10.10.2022
Tage bis Beginn: 314,0
Dosis: 3
Route/Site: IM / RA

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

Hypoxia Respiratory failure

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE HYPOXEMIC RESPIRATORY FAILURE, UNSPECIFIED ACUITY HYPOXIA

Weitere VAERSDATA-Felder

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

VAERS 2624847

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 02.05.2023
Impfdatum: 12.11.2021
Beginn: 13.10.2022
Tage bis Beginn: 335,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Moderna 3/7/21 Lot# 030A21A; Moderna 4/6/21 Lot# 018B21A; Moderna 11/12/21 Lot# 033F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2622149

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 89,0
Geschlecht: M
Eingang: 27.04.2023
Impfdatum: 10.11.2021
Beginn: 06.05.2022
Tage bis Beginn: 177,0
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 1/14/21 Lot# 012L20A; Moderna 2/11/21 Lot# 010M20A; Moderna 11/10/21 Lot# 033F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2619502

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: FL
Alter: 73,0
Geschlecht: F
Eingang: 23.04.2023
Impfdatum: 22.01.2021
Beginn: 01.01.2023
Tage bis Beginn: 709,0
Dosis: 1
Route/Site: SYR / RA

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

Acoustic stimulation tests normal Tinnitus

Symptomtext

Sometime after second dose started experiencing Tinitis.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acoustic stimulation tests normal
Hospital-Tage: -
Labordaten: Hearing evaluation done by doctor. He could not find any problems with my ears, and I have never had ear infections or difficulties with my ears. I also visited my dentist and investigated the possibility of a dental issue and none was found.
Aktuelle Erkrankungen: None
Vorgeschichte: Asthma
Andere Medikamente: Asthma inhaler/Multi Vitamins
Allergien: spring and fall allergies
Vorherige Impfungen: -

VAERS 2618398

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: 62,0
Geschlecht: M
Eingang: 20.04.2023
Impfdatum: 03.11.2021
Beginn: 01.08.2022
Tage bis Beginn: 271,0
Dosis: 3
Route/Site: IM / -

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

Transient ischaemic attack

Symptomtext

PATIENT RECEIVED VACCINE FROM OUTSIDE SOURCE TRANSIENT CEREBRAL ISCHEMIA

Weitere VAERSDATA-Felder

Praegender Schweregrund: Transient ischaemic attack
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2612278

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: 90,0
Geschlecht: M
Eingang: 10.04.2023
Impfdatum: 03.11.2021
Beginn: 07.12.2021
Tage bis Beginn: 34,0
Dosis: 3
Route/Site: IM / LA

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

Cardiac failure acute Left ventricular failure Obstructive sleep apnoea syndrome Oesophageal adenocarcinoma

Symptomtext

G47.33 ADULT OBSTRUCTIVE SLEEP APNEA, SEVERE 3/22/2022 ADENOCARCINOMA, LOWER THIRD OF ESOPHAGUS G47.33 ADULT OBSTRUCTIVE SLEEP APNEA, SEVERE 3/22/2022 LEFT HEART FAILURE G47.33 ADULT OBSTRUCTIVE SLEEP APNEA, SEVERE 3/22/2022 SYSTOLIC HEART FAILURE, ACUTE ON CHRONIC

Weitere VAERSDATA-Felder

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

VAERS 2606684

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 90,0
Geschlecht: M
Eingang: 30.03.2023
Impfdatum: 11.11.2021
Beginn: 21.05.2022
Tage bis Beginn: 191,0
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 3/27/21 Lot# 018B21A; Moderna 4/24/21 Lot# 043B21A; Moderna 11/11/21 Lot# 033F21

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2604104

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 40,0
Geschlecht: F
Eingang: 27.03.2023
Impfdatum: 03.12.2021
Beginn: 22.03.2023
Tage bis Beginn: 474,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Moderna 4/17/21 Lot# 047A21A; MOderna 5/8/21 Lot# 043B21A; MOderna 12/3/21 Lot# 033F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: external COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2592424

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 54,0
Geschlecht: F
Eingang: 07.03.2023
Impfdatum: 23.11.2021
Beginn: 27.02.2023
Tage bis Beginn: 461,0
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 3/18/21 Lot# 002B21A; Moderna 4/15/21 Lot# 040B21A; Moderna 11/23/21 Lot# 033F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2566631

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

gering

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 10.05.2022
Beginn: 23.01.2023
Tage bis Beginn: 258,0
Dosis: 3
Route/Site: SYR / UN

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

Aggression Agitation Anaemia Asthenia Azotaemia Blood creatinine increased COVID-19 Chest X-ray normal Haemoglobin decreased Laboratory test abnormal Mental status changes SARS-CoV-2 test positive

Symptomtext

82-year-old gentleman enrolled in palliative care w/ PMH of parkinson's disease, alzheimer psychosis possibly related to PD, HoH, pancreatic tumor (s/p resection) and GERD who presented from home to the ER on 1/23 w/ a CC of weakness. The patient was unable to participate in the history collection process due to underlying dementia. His wife and family therefore provided the history. The patient's wife noted that the day of admission he was talking to people who were not present and trying to push against walls. He has been increasingly agitated in recent times w/ adjustment to his risperidone which seemed to help at the time per family. He is currently enrolled in palliative care as per family he did not qualify for hospice. Patient's wife states that his wish was to be DNR/DNI.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Aggression
Hospital-Tage: 1,0
Labordaten: reviewed all the lab test results, EKG and radiological findings. CXR = no acute findings.The lab test results revealed a chronic anemia. The hemoglobin was 12.9. The creatinine was elevated at 1.4. There was a mild azotemia. The patient was hydrated with intravenous normal saline. Vital Signs: Temp (degrees F) ,98.6 Temp (degrees C) ,37 Temperature ,skin Heart Rate (beats/min) ,95 Respiration (breaths/min) ,24 SpO2 (%) ,100 BP Systolic (mm Hg) ,118 BP Diastolic (mm Hg) ,63 BP Mean (mm Hg) ,81 The patient tested positive for the COVID-19 infection. It was decided admit the patient for observation in view of an altered mental status. The patient received Ativan and Haldol after he exhibited a mild combativeness while being observed in the ED.
Aktuelle Erkrankungen: unknown
Vorgeschichte: DM HTN sleep apnea depression dementia parkinsons Alzheimer disease GERD
Andere Medikamente: Current Home Medications 1. carbidopa-levodopa 10 mg-100 mg oral tablet : 2 tab(s) orally 2 times a day 2. Effexor XR 75 mg oral capsule, extended release : 1 cap(s) orally once a day 3. memantine 5 mg oral tablet : 1 tab(s) orally 2 times
Allergien: Allergy: - null; (null) null - Gluten; (Food) Other See Desc
Vorherige Impfungen: -

VAERS 2566631

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

gering

Staat: MI
Alter: 81,0
Geschlecht: M
Eingang: 24.01.2023
Impfdatum: 10.05.2022
Beginn: 23.01.2023
Tage bis Beginn: 258,0
Dosis: 4
Route/Site: SYR / UN

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

Aggression Agitation Anaemia Asthenia Azotaemia Blood creatinine increased COVID-19 Chest X-ray normal Haemoglobin decreased Laboratory test abnormal Mental status changes SARS-CoV-2 test positive

Symptomtext

82-year-old gentleman enrolled in palliative care w/ PMH of parkinson's disease, alzheimer psychosis possibly related to PD, HoH, pancreatic tumor (s/p resection) and GERD who presented from home to the ER on 1/23 w/ a CC of weakness. The patient was unable to participate in the history collection process due to underlying dementia. His wife and family therefore provided the history. The patient's wife noted that the day of admission he was talking to people who were not present and trying to push against walls. He has been increasingly agitated in recent times w/ adjustment to his risperidone which seemed to help at the time per family. He is currently enrolled in palliative care as per family he did not qualify for hospice. Patient's wife states that his wish was to be DNR/DNI.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Aggression
Hospital-Tage: 1,0
Labordaten: reviewed all the lab test results, EKG and radiological findings. CXR = no acute findings.The lab test results revealed a chronic anemia. The hemoglobin was 12.9. The creatinine was elevated at 1.4. There was a mild azotemia. The patient was hydrated with intravenous normal saline. Vital Signs: Temp (degrees F) ,98.6 Temp (degrees C) ,37 Temperature ,skin Heart Rate (beats/min) ,95 Respiration (breaths/min) ,24 SpO2 (%) ,100 BP Systolic (mm Hg) ,118 BP Diastolic (mm Hg) ,63 BP Mean (mm Hg) ,81 The patient tested positive for the COVID-19 infection. It was decided admit the patient for observation in view of an altered mental status. The patient received Ativan and Haldol after he exhibited a mild combativeness while being observed in the ED.
Aktuelle Erkrankungen: unknown
Vorgeschichte: DM HTN sleep apnea depression dementia parkinsons Alzheimer disease GERD
Andere Medikamente: Current Home Medications 1. carbidopa-levodopa 10 mg-100 mg oral tablet : 2 tab(s) orally 2 times a day 2. Effexor XR 75 mg oral capsule, extended release : 1 cap(s) orally once a day 3. memantine 5 mg oral tablet : 1 tab(s) orally 2 times
Allergien: Allergy: - null; (null) null - Gluten; (Food) Other See Desc
Vorherige Impfungen: -

VAERS 2551345

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: OH
Alter: 30,0
Geschlecht: F
Eingang: 05.01.2023
Impfdatum: 07.12.2021
Beginn: 26.07.2022
Tage bis Beginn: 231,0
Dosis: 3
Route/Site: SYR / LA

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

Acoustic stimulation tests normal Tinnitus

Symptomtext

Since about July 26, 2021, I've been experiencing a ringing in my ears. It's constant in my right ear and comes and goes in my left ear. I've spoken to a couple of doctors about it. They prescribed prednisone for two weeks and told me I should speak to my regular doctor if the ringing in my ear didn't subside. The ringing got quieter, but the pitch got higher after taking prednisone. I spoke to my regular doctor. She didn't see anything wrong when she looked in my ears. She sent me to a specialist in November. They did a round of hearing tests. All results were within normal ranges. We're trying to schedule an MRI of my head. As of right now, there is no explanation or source for the ringing in my ears. I wasn't in contact with loud noises and didn't experience any injuries. It's a bit of a mystery right now.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acoustic stimulation tests normal
Hospital-Tage: -
Labordaten: 11/21/2022 hearing test normal ranges
Aktuelle Erkrankungen: Runny nose
Vorgeschichte: Scoliosis; Strabismus
Andere Medikamente: MIRENA IUD; NASACORT; multivitamin; vitamin D
Allergien: Seasonal ragweed
Vorherige Impfungen: -

VAERS 2529946

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: 81,0
Geschlecht: F
Eingang: 13.12.2022
Impfdatum: 18.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: IM / -

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

Herpes zoster Nervousness Stress Swelling face

Symptomtext

Case called health department 12-12-22 after she had scheduled herself for covid bibalent dose on 12-13-22.She wanted to check with nurse regarding her previous experience back in November when she stated she got a case of shingles approx.2 weeks after receiving her Moderna booster in November.She stated it involved swelling of the right side of her face.So she was nervous about getting the bivalent.She states that this was a stressful time for her as she was having to do some holiday decorating at her church and that this is always stressful for her.She recovered from this but I told her she should check with her provider about getting another dose of Moderna.Case cancelled Moderna bivalent appt.subsequently.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: denied
Vorgeschichte: case stated only condition is atrial fibrillation
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2528791

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 87,0
Geschlecht: F
Eingang: 12.12.2022
Impfdatum: 05.11.2021
Beginn: 06.12.2022
Tage bis Beginn: 396,0
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

COVID vaccine breakthrough case

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID positive test 12/09/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2522905

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: GA
Alter: 39,0
Geschlecht: F
Eingang: 05.12.2022
Impfdatum: 01.12.2021
Beginn: 01.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: SYR / LA

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

Amenorrhoea Blood test normal Female sex hormone level Menstrual disorder Menstruation irregular

Symptomtext

Starting sometime in the month of December of 2021, I developed amenorrhea. I usually have a menstrual cycle on the short side. After the 2nd dose, it would come every 21 days. Now, since receiving the booster, it comes every 4 months. I have been seeing a nurse/doctor and have gotten repeated blood work done with normal hormone levels and no indication of perimenopause or menopause. No other symptoms exist.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Amenorrhoea
Hospital-Tage: -
Labordaten: Lots of blood work: Normal hormone levels and no indication of perimenopause and menopause.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: Cashew; avocado; mango
Vorherige Impfungen: -

VAERS 2510309

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: OH
Alter: 35,0
Geschlecht: M
Eingang: 17.11.2022
Impfdatum: 02.11.2021
Beginn: -
Tage bis Beginn: -
Dosis: 1
Route/Site: OT / -

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

No adverse event Product administration interrupted

Symptomtext

Patient never received his 2nd dose of Moderna COVID-19 vaccine; No adverse event; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT ADMINISTRATION INTERRUPTED (Patient never received his 2nd dose of Moderna COVID-19 vaccine) and NO ADVERSE EVENT (No adverse event) in a 36-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 02-Nov-2021, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced PRODUCT ADMINISTRATION INTERRUPTED (Patient never received his 2nd dose of Moderna COVID-19 vaccine) and NO ADVERSE EVENT (No adverse event). At the time of the report, PRODUCT ADMINISTRATION INTERRUPTED (Patient never received his 2nd dose of Moderna COVID-19 vaccine) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessment was provided for PRODUCT ADMINISTRATION INTERRUPTED (Patient never received his 2nd dose of Moderna COVID-19 vaccine). No concomitant medications were reported. Patient never received the second dose. Patient has not reported any adverse reactions to the first dose. No treatment medications were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: No adverse event
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2506752

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: NY
Alter: 23,0
Geschlecht: F
Eingang: 13.11.2022
Impfdatum: 13.01.2022
Beginn: 19.04.2022
Tage bis Beginn: 96,0
Dosis: UNK
Route/Site: - / LA

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

Acoustic stimulation tests Tinnitus

Symptomtext

Tinnitus in left ear, no signs of hearing loss, increased ringing and clicking noises that are audible to others

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acoustic stimulation tests
Hospital-Tage: -
Labordaten: Saw an ENT and had a hearing test on 8/10/22
Aktuelle Erkrankungen: N/a
Vorgeschichte: Asthma Allergies
Andere Medikamente: Montelask Sudafed Claritin
Allergien: Strawberries Raspberries Kiwi Penicillin Sulfa drugs
Vorherige Impfungen: -

VAERS 2496493

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: NY
Alter: -
Geschlecht: U
Eingang: 02.11.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: IM / -

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

Expired product administered

Symptomtext

Moderna COVID 19 Vaccine was administered to 8 patients after the beyond use date. Director of Clinical Services and Vaccine Coordinator are working with local DOH to reconcile the errors and provide appropriate follow upto affected patients.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2488210

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 86,0
Geschlecht: M
Eingang: 25.10.2022
Impfdatum: 04.11.2021
Beginn: 22.10.2022
Tage bis Beginn: 352,0
Dosis: 3
Route/Site: - / -

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

COVID-19 SARS-CoV-2 test positive Vaccine breakthrough infection

Symptomtext

Breakthrough case admission after 3 vaccines Moderna 2/5/21 Lot# 011M20A; Moderna 3/5/21 Lot# 030A21A; Moderna 11/4/21 Lot# 033F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2475678

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: FL
Alter: 60,0
Geschlecht: M
Eingang: 11.10.2022
Impfdatum: 08.04.2022
Beginn: 07.09.2022
Tage bis Beginn: 152,0
Dosis: 4
Route/Site: IM / LA

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

COVID-19 SARS-CoV-2 test

Symptomtext

I contracted COVID-19 and became synonymous or about September 7, 2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID-19 Nasal Swab September 8, 2022
Aktuelle Erkrankungen: None
Vorgeschichte: Mild hypertension
Andere Medikamente: Hyzaar Allegra OTC Vit A, Vit B Complex, Vit D, Vit E, Uniquinol, Tonalin CLA, Magnesium, Zinc, Turmeric, Red Yeast Rice
Allergien: Latex Benadryl
Vorherige Impfungen: -

VAERS 2462916

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 84,0
Geschlecht: F
Eingang: 28.09.2022
Impfdatum: 16.11.2021
Beginn: 27.09.2022
Tage bis Beginn: 315,0
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 dose 1 3/3/21 011A21A dose 2 3/31/21 010M20A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: covid+ test on 9/27/22
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2449711

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

gering

Staat: OH
Alter: 83,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 02.12.2021
Beginn: 16.09.2022
Tage bis Beginn: 288,0
Dosis: 3
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

Admitted to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 1,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2449707

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

gering

Staat: KY
Alter: 87,0
Geschlecht: M
Eingang: 17.09.2022
Impfdatum: 28.10.2021
Beginn: 14.09.2022
Tage bis Beginn: 321,0
Dosis: 3
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

Admitted to hospital.

Weitere VAERSDATA-Felder

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

VAERS 2449646

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: 56,0
Geschlecht: F
Eingang: 17.09.2022
Impfdatum: 14.03.2021
Beginn: 30.11.2021
Tage bis Beginn: 261,0
Dosis: 2
Route/Site: - / -

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

COVID-19 COVID-19 immunisation Dysgeusia

Symptomtext

METALLIC TASTE; COVID-19; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient concerned a 58 year old female. The patient's height, and weight were not reported. The patient's past medical history included: iron deficiency, and lower back pain, and concurrent conditions included: codeine allergy. The patient was not pregnant at the time of the report. The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805022 expiry: UNKNOWN) dose was not reported, 1 total, administered on 14-MAR-2021 on left arm for covid-19 prophylaxis. Age at time of vaccination 56 years old. Concomitant medications included omeprazole (from 01-APR-2016) and zolpidem tartrate (Ambien, from JAN-2006) for unknown indication. It was unknown whether patient had any adverse events following vaccination with first dose of covid-19 vaccine ad26.cov2.s. (Dose number in series 1). The patient received non-company suspect vaccine elasomeran (Moderna covid-19 vaccine, Spikevax) (Dose number in series 2) (form of admin, route of admin were not reported, batch number: 033F21A expiry: UNKNOWN) dose was not reported, administered on 30-NOV-2021 on left arm for covid-19 prophylaxis which was revaccination with different covid-19 vaccine. On an unspecified date in 2022, the patient experienced metallic taste (which lasted 5 days), and covid-19 (fatigue, headache, diarrhea and night sweats) (Dose number in series 2). The patient received non-company suspect drug Nirmatrelvir/ritonavir (Paxlovid) (form of admin, route of admin were not reported, batch number: unknown expiry: UNKNOWN) dose was not reported, administered from 22-AUG-2022 to 27-AUG-2022 for covid-19 treatment. The action taken with covid-19 vaccine ad26.cov2.s and elasomeran was not applicable and with paxlovid treatment withdrawn on 27-AUG-2022. The patient recovered from metallic taste, and covid-19, and the outcome of revaccination with different covid-19 vaccine was not reported. This report was non-serious.; Sender's Comments: V0-Medical assessment comment not required as per standard procedure as the case is assessed as non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy
Vorgeschichte: Medical History/Concurrent Conditions: Iron deficiency; Low back pain; Comments: The patient was not pregnant at the time of the report.
Andere Medikamente: AMBIEN; OMEPRAZOLE
Allergien: -
Vorherige Impfungen: -

VAERS 2449290

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

gering

Staat: OH
Alter: 71,0
Geschlecht: M
Eingang: 17.09.2022
Impfdatum: 08.11.2021
Beginn: 08.09.2022
Tage bis Beginn: 304,0
Dosis: 3
Route/Site: IM / LA

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

Unevaluable event

Symptomtext

Admitted to hospital.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Unevaluable event
Hospital-Tage: 7,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2433621

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 94,0
Geschlecht: M
Eingang: 08.09.2022
Impfdatum: 05.02.2021
Beginn: 26.08.2022
Tage bis Beginn: 567,0
Dosis: 3
Route/Site: - / -

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

COVID-19 Hypoglycaemia SARS-CoV-2 test positive

Symptomtext

08/26/22 presents to ED due to "hypoglycemia". "no significant PMH"

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 08/27/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2433407

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 63,0
Geschlecht: F
Eingang: 08.09.2022
Impfdatum: 23.03.2021
Beginn: 11.08.2022
Tage bis Beginn: 506,0
Dosis: 3
Route/Site: - / -

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

Adrenocortical insufficiency acute COVID-19 Electrolyte imbalance SARS-CoV-2 test positive

Symptomtext

Patient admitted with COVID-19 that precipitated adrenal crisis, initially received IV hydrocortisone converted to oral therapy, patient has corrected electrolytes and has been given clearance for discharge per endocrinology.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Adrenocortical insufficiency acute
Hospital-Tage: 2,0
Labordaten: 8/11 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC-- detected
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: unknown
Vorherige Impfungen: -

VAERS 2417387

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: KS
Alter: 35,0
Geschlecht: M
Eingang: 22.08.2022
Impfdatum: 26.11.2021
Beginn: 04.12.2021
Tage bis Beginn: 8,0
Dosis: 3
Route/Site: SYR / RA

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

Acoustic stimulation tests abnormal Deafness Magnetic resonance imaging normal Scan with contrast normal Tinnitus

Symptomtext

Tinnitus

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acoustic stimulation tests abnormal
Hospital-Tage: -
Labordaten: MRI with contrast in January, normal results. Multiple hearing tests, mild hearing loss at 8khz only.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Propranolol
Allergien: None
Vorherige Impfungen: -

VAERS 2412440

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: OH
Alter: 85,0
Geschlecht: F
Eingang: 16.08.2022
Impfdatum: 16.01.2021
Beginn: 21.06.2022
Tage bis Beginn: 521,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19

Symptomtext

Admitted to hospital with COVID-19

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 6,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Arthritis, Asthma, Diabetes mellitus, Heart abnormalities, Hypertension, Kidney disease, and Stroke
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2405738

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 67,0
Geschlecht: M
Eingang: 09.08.2022
Impfdatum: 30.11.2021
Beginn: 08.08.2022
Tage bis Beginn: 251,0
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 4/12/21 Lot# 025B21A; Moderna 5/10/21 Lot# 018B21A; Moderna 11/30/21 Lot# 033F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: external COVID +
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2369001

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: 64,0
Geschlecht: F
Eingang: 14.07.2022
Impfdatum: 01.03.2022
Beginn: 28.06.2022
Tage bis Beginn: 119,0
Dosis: 3
Route/Site: IM / RA

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

COVID-19

Symptomtext

HOSPITALIZED DUE TO COVID

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 11,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2356025

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 03.07.2022
Impfdatum: 11.03.2021
Beginn: 05.11.2021
Tage bis Beginn: 239,0
Dosis: 2
Route/Site: OT / -

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

COVID-19 Dysgeusia Interchange of vaccine products

Symptomtext

metallic taste in mouth; for COVID-19 treatment; previously received COVID 19 vaccine AD26; This spontaneous case was reported by a consumer and describes the occurrence of DYSGEUSIA (metallic taste in mouth), COVID-19 (for COVID-19 treatment) and INTERCHANGE OF VACCINE PRODUCTS (previously received COVID 19 vaccine AD26) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for Prophylactic vaccination. Co-suspect product included non-company product COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) for Prophylactic vaccination. Concurrent medical conditions included Drug allergy and Cough (Using cough suppressant Robitussin). Concomitant products included ETHINYLESTRADIOL, NORGESTIMATE (TRI-LO-SPRINTEC) for Birth control, DEXTROMETHORPHAN HYDROBROMIDE, ETHANOL, GUAIFENESIN (ROBITUSSIN [DEXTROMETHORPHAN HYDROBROMIDE;ETHANOL;GUAIFENESIN]) for Cough suppression. On 11-Mar-2021, the patient received first dose of COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) (unknown route) 1 dosage form. On 05-Nov-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-Nov-2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (previously received COVID 19 vaccine AD26). On 25-May-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced DYSGEUSIA (metallic taste in mouth). In 2022, the patient experienced COVID-19 (for COVID-19 treatment). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) on 25-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, DYSGEUSIA (metallic taste in mouth), COVID-19 (for COVID-19 treatment) and INTERCHANGE OF VACCINE PRODUCTS (previously received COVID 19 vaccine AD26) outcome was unknown. It was reported that event Suspected COVID-19 received treatment. Patient was on contraceptive therapy using Tri-Lo-Sprintec currently. It was reported that Patient was taking other medications/Products within 2 weeks of initiating covid-19 treatment. It was reported that this case was associated with product quality compliant number: 90000235217 Sender/company comment: Covid-19 vaccine ad26.cov2. s-suspected clinical vaccination failure. The events has an unknown/unclear temporal relationship, was unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the events than the drug. Specifically special situations. Therefore this events is considered as not related. Company Comment: This is a spontaneous case of Interchange of vaccine products concerning a patient of unspecified age and sex, previously vaccinated with a dose of COVID-19 AD26 (dose 1 in COVID-19 vaccine series), with a medical history of suspected COVID-19 following COVID-19 AD26 vaccine, who experienced the unexpected non-serious events of COVID-19 (AESI) and Dysgeusia (metallic taste in mouth). Event COVID-19 occurred unspecified number of days after receiving a dose of mRNA-1273 Vaccine, dose 2 in vaccine series while event Dysgeusia occurred approximately 6 ? months after vaccination, same day that Paxlovid was started for COVID-19 treatment. Event dysgeusia can also be related to COVID-19. There is no available information regarding clinical course. Paxlovid treatment remains a confounder for event dysgeusia as this can be an adverse effect of the said drug. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.; Sender's Comments: This is a spontaneous case of Interchange of vaccine products concerning a patient of unspecified age and sex, previously vaccinated with a dose of COVID-19 AD26 (dose 1 in COVID-19 vaccine series), with a medical history of suspected COVID-19 following COVID-19 AD26 vaccine, who experienced the unexpected non-serious events of COVID-19 (AESI) and Dysgeusia (metallic taste in mouth). Event COVID-19 occurred unspecified number of days after receiving a dose of mRNA-1273 Vaccine, dose 2 in vaccine series while event Dysgeusia occurred approximately 6 ? months after vaccination, same day that Paxlovid was started for COVID-19 treatment. Event dysgeusia can also be related to COVID-19. There is no available information regarding clinical course. Paxlovid treatment remains a confounder for event dysgeusia as this can be an adverse effect of the said drug. 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: Cough (Using cough suppressant Robitussin); Drug allergy
Vorgeschichte: -
Andere Medikamente: TRI-LO-SPRINTEC; ROBITUSSIN [DEXTROMETHORPHAN HYDROBROMIDE;ETHANOL;GUAIFENESIN]
Allergien: -
Vorherige Impfungen: -

VAERS 2334973

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: 40,0
Geschlecht: M
Eingang: 25.06.2022
Impfdatum: 20.03.2021
Beginn: 31.10.2021
Tage bis Beginn: 225,0
Dosis: 2
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 Vaccination failure

Symptomtext

COVID-19 infection; Confirmed Clinical Vaccination Failure; Received first dose Janssen, second and third dose Moderna; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (COVID-19 infection) and VACCINATION FAILURE (Confirmed Clinical Vaccination Failure) in a 39-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) for Prophylactic vaccination. Concurrent medical conditions included Drug allergy. On 20-Mar-2021, the patient received first dose of COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) (unknown route) 1 dosage form. On 31-Oct-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-May-2022, received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 31-Oct-2021, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Received first dose Janssen, second and third dose Moderna). On 10-May-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced COVID-19 (COVID-19 infection) (seriousness criterion medically significant) and VACCINATION FAILURE (Confirmed Clinical Vaccination Failure) (seriousness criterion medically significant). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 10-May-2022 to 15-May-2022 for COVID-19 treatment, at a dose of 1 UNK. At the time of the report, COVID-19 (COVID-19 infection) had not resolved and VACCINATION FAILURE (Confirmed Clinical Vaccination Failure) and INTERCHANGE OF VACCINE PRODUCTS (Received first dose Janssen, second and third dose Moderna) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 10-May-2022, SARS-CoV-2 test: positive (Positive) Positive. On 20-May-2022, SARS-CoV-2 test: positive (Positive) Positive thick and clear line. On an unknown date, SARS-CoV-2 test: positive (Positive) Positive result with a fading positive line. No concomitant medication was provided. The patient was not taking any other medications/products within 2 weeks of starting Covid-19 treatment. On 31-Oct-2021, the patient received booster dose of Spikevax. Patient began to take paxlovid (confirmed clinical vaccination failure) for Covid-19 treatment. He took full course of pills and felt better each day, several home antigen tests and each one showed a positive result but with a fading positive line. On 20-May-2022 the patient felt the symptoms returning and he took another test and found the positive line thick and clear which indicated that his viral load had increased since getting off paxlovid. Company Comment: This spontaneous case reported by a patient concerns a 40-year-old male patient, with no relevant medical history, who experienced unexpected, serious (medically significant) AESI Covid-19 (laboratory confirmed) around 4 days after receiving a booster dose of mRNA-1273 (third dose in a Covid19 vaccination schedule). Vaccination failure was also reported. He was treated with a course of Paxlovid and was starting to feel better. However, 5 days after Paxlovid completion the patient felt symptoms returning and tested positive again for Covid19. Additionally, the patient previously received a different Covid19 vaccine Janssen as his initial dose (interchange of vaccine products). The ongoing Covid19 pandemic could be a contributory factor. The benefit risk relationship of mRNA-1273 is not affected by this report. Reporter did not allow further contact; Sender's Comments: This spontaneous case reported by a patient concerns a 40-year-old male patient, with no relevant medical history, who experienced unexpected, serious (medically significant) AESI Covid-19 (laboratory confirmed) around 4 days after receiving a booster dose of mRNA-1273 (third dose in a Covid19 vaccination schedule). Vaccination failure was also reported. He was treated with a course of Paxlovid and was starting to feel better. However, 5 days after Paxlovid completion the patient felt symptoms returning and tested positive again for Covid19. Additionally, the patient previously received a different Covid19 vaccine Janssen as his initial dose (interchange of vaccine products). The ongoing Covid19 pandemic could be a contributory factor. The benefit risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Name: Covid 19 Antigen test; Test Result: Positive ; Result Unstructured Data: Positive result with a fading positive line; Test Date: 20220510; Test Name: Covid 19 Antigen test; Test Result: Positive ; Result Unstructured Data: Positive; Test Date: 20220520; Test Name: Covid 19 Antigen test; Test Result: Positive ; Result Unstructured Data: Positive thick and clear line
Aktuelle Erkrankungen: Drug allergy
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2319968

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 15.06.2022
Impfdatum: 17.03.2022
Beginn: 17.03.2022
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 dose administered after vaccine reached Beyond Use Date (BUD); This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (1 dose administered after vaccine reached Beyond Use Date (BUD)) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 033F21A) for COVID-19 prophylaxis. No Medical History information was reported. On 17-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 17-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (1 dose administered after vaccine reached Beyond Use Date (BUD)). At the time of the report, EXPIRED PRODUCT ADMINISTERED (1 dose administered after vaccine reached Beyond Use Date (BUD)) outcome was unknown. The action taken with mRNA-1273 (Spikevax) (Unknown) was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was reported. It was reported that the vaccine was in refrigerator and was administered after Beyond Use Date (BUD) which was 06-Dec-2021. 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 2319919

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 15.06.2022
Impfdatum: 11.03.2021
Beginn: 25.05.2022
Tage bis Beginn: 440,0
Dosis: 2
Route/Site: - / -

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

Dysgeusia Suspected COVID-19 Vaccination failure

Symptomtext

SUSPECTED CLINICAL VACCINATION FAILURE; SUSPECTED COVID-19 INFECTION; METALLIC TASTE IN MOUTH; This spontaneous report received from a patient concerned a patient of an unspecified age, sex, race and ethnic origin. Initial information was processed along with the additional information received on 10-JUN-2022. The patient's height, and weight were not reported. The patient's concomitant medical history included: Drug allergy. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805018 expiry: UNKNOWN) dose was not reported, 01 total administered on 11-MAR-2021 for prophylactic vaccination. On an unspecified date, following vaccination with covid-19 vaccine ad26.cov2.s, the patient had Covid-19 (coded as suspected covid-19 and suspected clinical vaccination failure) (Dose number in series 1) and received treatment. The patient was taking other medications/products within 2 weeks of initiation of COVID-19 treatment (Dose number in series 1). The patient additionally received non-company suspect vaccine elasomeran (Moderna Covid-19 vaccine) (dose number in series 2) (form of admin, route of admin were not reported, batch number: 033F21A expiry: UNKNOWN) dose was not reported, administered on 05-NOV-2021 for prophylactic vaccination. Concomitant medications included ethinylestradiol/norgestimate for birth control, and dextromethorphan hydrobromide/ethanol/guaifenesin for cough suppressant. The patient received non-company suspect drug Plaxovid (form of admin, route of admin, batch number were not reported), dose was not reported administered on 25-MAY-2022 for Covid-19 treatment. On 25-MAY-2022, the patient experienced metallic taste in mouth (dose number in series 2). The action taken with covid-19 vaccine ad26.cov2.s, and elasomeran was not applicable, and for Plaxovid not reported. The outcome of the metallic taste in mouth, suspected covid-19 infection and suspected clinical vaccination failure was not reported. This case is associated with product quality complaint number: 90000235217. This report was serious (Other Medically Important Condition).; Sender's Comments: V0-20220609401-covid-19 vaccine ad26.cov2.s-Suspected clinical vaccination failure. The event(s) has an unknown/unclear temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dysgeusia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy
Vorgeschichte: -
Andere Medikamente: TRI-LO-SPRINTEC; ROBITUSSIN [DEXTROMETHORPHAN HYDROBROMIDE;ETHANOL;GUAIFENESIN]
Allergien: -
Vorherige Impfungen: -

VAERS 2313683

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MA
Alter: 37,0
Geschlecht: F
Eingang: 09.06.2022
Impfdatum: 01.11.2021
Beginn: 03.06.2022
Tage bis Beginn: 214,0
Dosis: 3
Route/Site: OT / LA

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

COVID-19 SARS-CoV-2 test

Symptomtext

Reporting covid rebound, By today, 03-Jun, my rapid tests were solidly positive once again; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (Reporting covid rebound, By today, 03-Jun, my rapid tests were solidly positive once again) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. Co-suspect product included non-company product NIRMATRELVIR, RITONAVIR (PAXLOVID) for COVID-19 treatment. Relevant past drug history reported as, name of drug : no and reaction reported as Allergy. Previously administered products included for Product used for unknown indication: Pfizer/Biontech (Dose number: 1, Batch/lot No: EWO151, Location of injection: Arm left) on 08-Apr-2021, Pfizer/Biontech (Dose number: 2, Batch/Lot No: EW0171 and Location of injection: Arm left) on 29-Apr-2021. Past adverse reactions to the above products included No adverse event with Pfizer/Biontech and Pfizer/Biontech. On 01-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 26-May-2022, the patient started NIRMATRELVIR, RITONAVIR (PAXLOVID) (unknown route) at an unspecified dose. On 03-Jun-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced COVID-19 (Reporting covid rebound, By today, 03-Jun, my rapid tests were solidly positive once again). At the time of the report, COVID-19 (Reporting covid rebound, By today, 03-Jun, my rapid tests were solidly positive once again) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 31-May-2022, SARS-CoV-2 test: negative (Negative) Negative. On 03-Jun-2022, SARS-CoV-2 test: positive (Positive) Positive. Reported that the patient was not taking any other medications/products within 2 weeks of starting COVID- 19 treatment. No concomitant medication information provided. Reported that covid rebound, patient took Paxlovid and was thrilled to test negative for Covid on May 31 on two different rapid tests, after patient finished course of Paxlovid. Over the next few days patient went between testing negative and having a faint positive line on rapid tests. Assumed it was clearing the system. By today, 3-Jun, rapid tests were solidly positive once again. Device Date 03-Jun-2022. Company comment: This spontaneous case concerns a 37-year-old female patient with no relevant medical history reported, who experienced the unexpected non-serious AESI event of COVID-19, which occured 7 months after receiving third dose of mRNA-1273 vaccine. It was reported that patient was treated with Paxlovid from 26-may-2022 to 30-may-202. She was tested positive 2 days after the treatment with Paxlovid. Patient had received 2 doses of Comirnaty COVID-19 vaccine approximately 6 3 months prior to mRNA-1273 vaccination (Interchange of vaccine products). The current pandemic situation of COVID 19 may remain as confounder to the event Covid-19. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.; Sender's Comments: This spontaneous case concerns a 37-year-old female patient with no relevant medical history reported, who experienced the unexpected non-serious AESI event of COVID-19, which occured 7 months after receiving third dose of mRNA-1273 vaccine. It was reported that patient was treated with Paxlovid from 26-may-2022 to 30-may-202. She was tested positive 2 days after the treatment with Paxlovid. Patient had received 2 doses of Comirnaty COVID-19 vaccine approximately 6 3 months prior to mRNA-1273 vaccination (Interchange of vaccine products). The current pandemic situation of COVID 19 may remain as confounder to the event Covid-19. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220531; Test Name: COVID-19 virus test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220603; Test Name: COVID-19 virus test; Test Result: Positive ; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Comments: Relevant past drug history reported as, name of drug : no and reaction reported as Allergy.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2310324

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: CT
Alter: 46,0
Geschlecht: M
Eingang: 06.06.2022
Impfdatum: 03.12.2021
Beginn: 01.02.2022
Tage bis Beginn: 60,0
Dosis: 3
Route/Site: SYR / AR

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

Amnesia Blood test Cerumen removal Ear congestion Ear discomfort Feeling abnormal Keratosis obturans Laboratory test Lipids Mental impairment

Symptomtext

I have problems with my ears, heavy thinking, and brain fog. I went to my doctor and they ran some test. They said I have short term memory loss and my eardrums were blocked. The EMT said I had Keratosis Obturans. He removed the keratin. Things has gotten better since he has removed it. There is no known cause as to why it develops.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Amnesia
Hospital-Tage: -
Labordaten: Neurological test, blood work, lipid panel.
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: None
Allergien: None
Vorherige Impfungen: I felt sick after receiving the 1st Dose (3/272021) and 2nd dose (4/24/2021) of the Covid vaccines.

VAERS 2308024

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: RI
Alter: 48,0
Geschlecht: F
Eingang: 03.06.2022
Impfdatum: 12.04.2021
Beginn: 30.05.2022
Tage bis Beginn: 413,0
Dosis: UNK
Route/Site: OT / -

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

COVID-19 Drug ineffective SARS-CoV-2 test Interchange of vaccine products

Symptomtext

COVID 19 Treatment; COVID 19 Treatment; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 49-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 12Apr2021 as dose 1, single (Lot number: ER8735) and on 05May2021 as dose 2, single (Lot number: EW0170) for covid-19 immunisation; coviD-19 vaccine mrna (mrna 1273) (MODERNA COVID-19 VACCINE), on 08Nov2021 as dose number unknown (booster), single (Lot number: 033F21A) for covid-19 immunisation. The patient's relevant medical history included: "Penicillin" (unspecified if ongoing); "plastic adhesive bandages" (unspecified if ongoing); "Elevated blood pressure" (unspecified if ongoing); "raynaud's syndrome" (unspecified if ongoing); "hypothyroidism" (unspecified if ongoing); "eczema" (unspecified if ongoing); "rosacea" (unspecified if ongoing). Concomitant medication(s) included: JUNEL; LOSARTAN POTASSIUM, start date: 26Apr2022; LEVOTHYROXINE; SPIRONOLACTONE; DULOXETINE. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant) all with onset 30May2022, outcome "not recovered" and all described as "COVID 19 Treatment". The patient underwent the following laboratory tests and procedures: SARS-CoV-2 test: (20May2022) Negative; (30May2022) positive. Therapeutic measures were taken as a result of drug ineffective, covid-19. No follow-up attempts are possible. No further information is expected.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220520; Test Name: covid test; Test Result: Negative ; Test Date: 20220530; Test Name: covid test; Test Result: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Adhesive tape allergy; Blood pressure high; Eczema; Hypothyroidism; Penicillin allergy; Raynaud's syndrome; Rosacea
Andere Medikamente: JUNEL; LOSARTAN POTASSIUM; LEVOTHYROXINE; SPIRONOLACTONE; DULOXETINE
Allergien: -
Vorherige Impfungen: -

VAERS 2306858

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: GA
Alter: 30,0
Geschlecht: M
Eingang: 02.06.2022
Impfdatum: 05.05.2022
Beginn: 08.05.2022
Tage bis Beginn: 3,0
Dosis: 2
Route/Site: IM / LA

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

Dysphonia

Symptomtext

Vocal quality change (weak, breathy) started 3 days following Moderna vaccination on 5/5/22.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Dysphonia
Hospital-Tage: -
Labordaten: Treated with oral steroids and omeprazole
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: no known drug allergies
Vorherige Impfungen: -

VAERS 2306115

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: -
Geschlecht: U
Eingang: 02.06.2022
Impfdatum: 05.11.2021
Beginn: 25.05.2022
Tage bis Beginn: 201,0
Dosis: 2
Route/Site: OT / -

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

COVID-19 Dysgeusia

Symptomtext

COVID-19/Treatment of COVID-19; Metallic taste; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (COVID-19/Treatment of COVID-19) and DYSGEUSIA (Metallic taste) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Jansen (Dose Number: 1 Batch/Lot No: 1805018) on 11-Mar-2021. Past adverse reactions to the above products included No adverse event with Jansen. Concurrent medical conditions included Allergy. Concomitant products included ETHINYLESTRADIOL, NORGESTIMATE (TRI-LO-SPRINTEC) and MENTHOL (ROBITUSSIN [MENTHOL]) for an unknown indication. On 05-Nov-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-May-2022, the patient experienced COVID-19 (COVID-19/Treatment of COVID-19) and DYSGEUSIA (Metallic taste). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) on 25-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, COVID-19 (COVID-19/Treatment of COVID-19) and DYSGEUSIA (Metallic taste) outcome was unknown. Not Provided Patient was taking any other medications or products within 2 weeks of starting COVID-19 treatment. Device Date was reported as 26-May-2022 Active Drug substance name for Robitussin was reported as Cough suppressant Active Drug substance name for Trilosprintec was reported as Birth control Company comment: This spontaneous case concerns a patient of unknown age and gender, with no reported relevant medical history, who experienced, unexpected, non-serious, of COVID-19, approximately 6 months after receiving mRNA-1273 vaccine as a second dose, along with non-serious event of Dysgeusia. Interchange of vaccine products is noted in this case since the patient reported receiving 1 dose of Janssen, approximately 8 months before receiving mRNA-1273 vaccine. The patient was started with Nirmatrelvir-Ritonavir (Paxlovid) dose, duration and frequency were unknown. Clinical course, treatment details and diagnostic tests are not available in this report. The outcome of the event was unknown. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case concerns a patient of unknown age and gender, with no reported relevant medical history, who experienced, unexpected, non-serious, of COVID-19, approximately 6 months after receiving mRNA-1273 vaccine as a second dose, along with non-serious event of Dysgeusia. Interchange of vaccine products is noted in this case since the patient reported receiving 1 dose of Janssen, approximately 8 months before receiving mRNA-1273 vaccine. The patient was started with Nirmatrelvir-Ritonavir (Paxlovid) dose, duration and frequency were unknown. Clinical course, treatment details and diagnostic tests are not available in this report. The outcome of the event was unknown. The benefit-risk relationship of mRNA-1273 is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: Medical History/Concurrent Conditions: Allergy
Andere Medikamente: TRI-LO-SPRINTEC; ROBITUSSIN [MENTHOL]
Allergien: -
Vorherige Impfungen: -

VAERS 2299615

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: CA
Alter: 39,0
Geschlecht: M
Eingang: 02.06.2022
Impfdatum: 31.10.2021
Beginn: 10.05.2022
Tage bis Beginn: 191,0
Dosis: 2
Route/Site: OT / -

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

CONFIRMED COVID-19 INFECTION; CONFIRMED CLINICAL VACCINATION FAILURE; This spontaneous report received from a patient via Pfizer (other manufacturer) concerned a 40 year old male. Initial information was processed along with the additional information received on 31-MAY-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: drug allergy, and other pre-existing medical conditions included: The patient was not taking any other medications/products within 2 weeks of starting COVID-19 treatment. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of administration not reported, batch number: 1805018, expiry: unknown) dose was not reported, 1 total, administered on left arm on 20-MAR-2021 for prophylactic vaccination. Age at the time of vaccination was 39 years. No concomitant medications were reported. The patient additionally received booster dose of non-company suspect vaccine Spikevax (elasomeran) (dose 1 of dose number in series 2) (form of administration and route of administration was not reported, batch number: 033F21A and expiry: unknown) 1 total, dose was not reported, administered on left arm on 31-OCT-2021 for prophylactic vaccination. The patient received another dose of Spikevax (elasomeran) (dose 2 of dose number in series 2) (form of administration, route of administration and batch number were not reported and expiry: unknown) dose was not reported, 1 total, administered on left arm on 06-MAY-2022 for prophylactic vaccination. On 10-MAY-2022, tested positive for Covid and was prescribed Paxlovid (confirmed clinical vaccination failure) (dose number in series 1). The patient began taking Paxlovid (batch number: FY0461) on 10-MAY-2022 and completed the 5-day treatment on 15-MAY-2022 for Covid-19 treatment. The patient took full course of pills and felt better each day. He took several home antigen tests and each one showed a positive result (confirmed Covid-19 infection) (dose number in series 2) but with a fading positive line. On 20-MAY-2022, the patient felt the symptoms returning and he took another test and found the positive line thick and clear which indicated that his viral load had increased since getting off Paxlovid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from confirmed covid-19 infection and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality compliant: 90000233604.; Sender's Comments: V0: 20220558520- covid-19 vaccine ad26.cov2.s-confirmed clinical vaccination failure. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220510; Test Name: COVID-19 virus test; Result Unstructured Data: Positive; Comments: Positive; Test Date: 20220520; Test Name: COVID-19 antigen test; Result Unstructured Data: Positive thick and clear line; Comments: Positive thick and clear line; Test Name: COVID-19 antigen test; Result Unstructured Data: Positive result; Comments: Positive result with a fading positive line
Aktuelle Erkrankungen: Drug allergy
Vorgeschichte: Comments: The patient was not taking any other medications/products within 2 weeks of starting COVID-19 treatment.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2299615

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: CA
Alter: 39,0
Geschlecht: M
Eingang: 02.06.2022
Impfdatum: 31.10.2021
Beginn: 10.05.2022
Tage bis Beginn: 191,0
Dosis: UNK
Route/Site: OT / LA

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

COVID-19 SARS-CoV-2 test Vaccination failure

Symptomtext

CONFIRMED COVID-19 INFECTION; CONFIRMED CLINICAL VACCINATION FAILURE; This spontaneous report received from a patient via Pfizer (other manufacturer) concerned a 40 year old male. Initial information was processed along with the additional information received on 31-MAY-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: drug allergy, and other pre-existing medical conditions included: The patient was not taking any other medications/products within 2 weeks of starting COVID-19 treatment. The patient previously received covid-19 vaccine ad26.cov2.s (dose number in series 1) (suspension for injection, route of administration not reported, batch number: 1805018, expiry: unknown) dose was not reported, 1 total, administered on left arm on 20-MAR-2021 for prophylactic vaccination. Age at the time of vaccination was 39 years. No concomitant medications were reported. The patient additionally received booster dose of non-company suspect vaccine Spikevax (elasomeran) (dose 1 of dose number in series 2) (form of administration and route of administration was not reported, batch number: 033F21A and expiry: unknown) 1 total, dose was not reported, administered on left arm on 31-OCT-2021 for prophylactic vaccination. The patient received another dose of Spikevax (elasomeran) (dose 2 of dose number in series 2) (form of administration, route of administration and batch number were not reported and expiry: unknown) dose was not reported, 1 total, administered on left arm on 06-MAY-2022 for prophylactic vaccination. On 10-MAY-2022, tested positive for Covid and was prescribed Paxlovid (confirmed clinical vaccination failure) (dose number in series 1). The patient began taking Paxlovid (batch number: FY0461) on 10-MAY-2022 and completed the 5-day treatment on 15-MAY-2022 for Covid-19 treatment. The patient took full course of pills and felt better each day. He took several home antigen tests and each one showed a positive result (confirmed Covid-19 infection) (dose number in series 2) but with a fading positive line. On 20-MAY-2022, the patient felt the symptoms returning and he took another test and found the positive line thick and clear which indicated that his viral load had increased since getting off Paxlovid. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient had not recovered from confirmed covid-19 infection and the outcome of confirmed clinical vaccination failure was not reported. This report was serious (Other Medically Important Condition). This report was associated with a product quality compliant: 90000233604.; Sender's Comments: V0: 20220558520- covid-19 vaccine ad26.cov2.s-confirmed clinical vaccination failure. The event(s) has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event(s) than the drug. Specifically: SPECIAL SITUATIONS. Therefore, this event(s) is considered not related.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220510; Test Name: COVID-19 virus test; Result Unstructured Data: Positive; Comments: Positive; Test Date: 20220520; Test Name: COVID-19 antigen test; Result Unstructured Data: Positive thick and clear line; Comments: Positive thick and clear line; Test Name: COVID-19 antigen test; Result Unstructured Data: Positive result; Comments: Positive result with a fading positive line
Aktuelle Erkrankungen: Drug allergy
Vorgeschichte: Comments: The patient was not taking any other medications/products within 2 weeks of starting COVID-19 treatment.
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2303580

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 77,0
Geschlecht: M
Eingang: 31.05.2022
Impfdatum: 05.11.2021
Beginn: 25.05.2022
Tage bis Beginn: 201,0
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 #1 Moderna 2/17/21 Lot # 015M20A #2 Moderna 3/17/21 Lot# 002B21A #3 Moderna 11/5/21 Lot# 033F21A

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 5/25/22 external COVID-19 +.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2303102

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: CA
Alter: 46,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 01.11.2021
Beginn: 01.05.2022
Tage bis Beginn: 181,0
Dosis: 3
Route/Site: OT / -

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

COVID-19 SARS-CoV-2 test

Symptomtext

Rebound COVID/ I was positive again on rapid antigen test; This spontaneous case was reported by a nurse and describes the occurrence of COVID-19 (Rebound COVID/ I was positive again on rapid antigen test) in a 46-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. Co-suspect product included non-company product NIRMATRELVIR, RITONAVIR (PAXLOVID) for COVID-19 treatment. Concomitant products included ETHINYLESTRADIOL, ETONOGESTREL (NUVARING) from 01-Sep-2019 to 25-May-2022 for an unknown indication. On 01-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-May-2022, the patient started NIRMATRELVIR, RITONAVIR (PAXLOVID) (unknown route) at an unspecified dose. In May 2022, the patient experienced COVID-19 (Rebound COVID/ I was positive again on rapid antigen test). At the time of the report, COVID-19 (Rebound COVID/ I was positive again on rapid antigen test) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 13-May-2022, SARS-CoV-2 test: positive (Positive) Positive. In May 2022, SARS-CoV-2 test: positive (Positive) Positive. On 17-May-2022, SARS-CoV-2 test: negative (Negative) Negative. On 23-May-2022, SARS-CoV-2 test: negative (Negative) Negative. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Reportedly, the patient was taking other medications/products within 2 weeks of starting COVID-19 treatment. Patient was originally tested positive on 13-May-2022 but symptoms started in the evening of 12-May-2022 and her COVID symptoms started to improve on 15-May-2022. Patient never felt completely 100 percent, but she continued to improve. Patient started testing negative on 17-May-2022 on home rapid antigen. Patient had started to feel unwell again on the evening of 23-May-2022 and woke up on 24-May-2022 with congestion and cough. By the afternoon, she had a low grade fever and worsening congestion/cough/headache. Patient assumed she was getting a secondary sinus infection, but had been reading about rebound COVID, so tested herself and was negative on 23-May-2022 and was positive again on rapid antigen test. No treatment information was provided. Device Date was reported as 25-May-2022. Company comment: This spontaneous case concerns a 46-year-old female patient with no reported medical history, who experienced the unexpected, non-serious adverse event of special interest COVID-19 (with a positive SARS-CoV-2 test). The event occurred after administration of third dose of mRNA-1273 approximately 6 months prior, the exact date of onset of the event was not specified. There was no information provided regarding the initial two doses. On May 13, 2022, the patient took a SARS-CoV-2 which revealed a positive result, the test yielded a negative result on May 17 and 23, 2022. It has been reported that the patient never felt completely well but had improving conditions. Patient had started to feel unwell again on the evening of May 23, 2022, and woke the next day with congestion, cough, headache and low-grade fever. Outcome of the events was unknown at the time of this report. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.; Sender's Comments: This spontaneous case concerns a 46-year-old female patient with no reported medical history, who experienced the unexpected, non-serious adverse event of special interest COVID-19 (with a positive SARS-CoV-2 test). The event occurred after administration of third dose of mRNA-1273 approximately 6 months prior, the exact date of onset of the event was not specified. There was no information provided regarding the initial two doses. On May 13, 2022, the patient took a SARS-CoV-2 which revealed a positive result, the test yielded a negative result on May 17 and 23, 2022. It has been reported that the patient never felt completely well but had improving conditions. Patient had started to feel unwell again on the evening of May 23, 2022, and woke the next day with congestion, cough, headache and low-grade fever. Outcome of the events was unknown at the time of this report. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 202205; Test Name: COVID-19 rapid antigen; Test Result: Positive ; Result Unstructured Data: Positive; Test Date: 20220517; Test Name: COVID-19 rapid antigen; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220523; Test Name: COVID-19 rapid antigen; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220513; Test Name: COVID-19 Test; Test Result: Positive ; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: NUVARING; PAXLOVID
Allergien: -
Vorherige Impfungen: -

VAERS 2303006

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MA
Alter: 27,0
Geschlecht: F
Eingang: 31.05.2022
Impfdatum: 05.11.2021
Beginn: 23.05.2022
Tage bis Beginn: 199,0
Dosis: 3
Route/Site: OT / LA

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

COVID-19

Symptomtext

Rebound COVID symptoms; This spontaneous case was reported by a nurse and describes the occurrence of COVID-19 (Rebound COVID symptoms) in a 27-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. Co-suspect product included non-company product NIRMATRELVIR, RITONAVIR (PAXLOVID) for COVID-19 treatment. The patient's past medical history included GERD and Anxiety. Concurrent medical conditions included Soy allergy (Soy), Penicillin allergy (Penicillin) and Drug allergy. Concomitant products included GUAIFENESIN from 12-May-2022 to 15-May-2022 for an unknown indication. On 05-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-May-2022, the patient started NIRMATRELVIR, RITONAVIR (PAXLOVID) (unknown route) at an unspecified dose. On 23-May-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced COVID-19 (Rebound COVID symptoms). At the time of the report, COVID-19 (Rebound COVID symptoms) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient was taking other medication within 2 weeks of starting COVID-19 treatment. Patient reported that she had rebound of COVID-19 symptoms. No treatment information was provided. Device date was 24-May-2022. Company comment: This spontaneous case concerns a 27-year-old female patient with no relevant medical history reported, who experienced the unexpected non-serious AESI event of COVID-19,which occurred 168 after receiving third dose of mRNA-1273 vaccine. It was reported that patient was treated with Paxlovid from 13-may-2022 to 17-may-2022. She was tested positive 6 days after the treatment with Paxlovid, The current pandemic situation of COVID 19 may remain as confounder to the event Covid-19. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.; Sender's Comments: Company comment: This spontaneous case concerns a 27-year-old female patient with no relevant medical history reported, who experienced the unexpected non-serious AESI event of COVID-19,which occurred 168 after receiving third dose of mRNA-1273 vaccine. It was reported that patient was treated with Paxlovid from 13-may-2022 to 17-may-2022. She was tested positive 6 days after the treatment with Paxlovid, The current pandemic situation of COVID 19 may remain as confounder to the event Covid-19. 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: Drug allergy; Penicillin allergy (Penicillin); Soy allergy (Soy)
Vorgeschichte: Medical History/Concurrent Conditions: Anxiety; GERD
Andere Medikamente: GUAIFENESIN; PAXLOVID
Allergien: -
Vorherige Impfungen: -

VAERS 2301809

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MD
Alter: 71,0
Geschlecht: M
Eingang: 30.05.2022
Impfdatum: 31.10.2021
Beginn: 11.05.2022
Tage bis Beginn: 192,0
Dosis: 3
Route/Site: OT / LA

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

COVID-19 SARS-CoV-2 test

Symptomtext

recurred Covid 19; This spontaneous case was reported by a physician and describes the occurrence of COVID-19 (recurred Covid 19) in a 71-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. Concurrent medical conditions included Asthma. Concomitant products included ATORVASTATIN CALCIUM (LIPITOR) from 04-May-2022 to an unknown date and TERBINAFINE HYDROCHLORIDE (LAMISIL [TERBINAFINE HYDROCHLORIDE]) from 04-May-2022 to an unknown date for an unknown indication. On 31-Oct-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-May-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced COVID-19 (recurred Covid 19). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 13-May-2022 to 16-May-2022 for COVID-19 treatment, at a dose of 1 dosage form. At the time of the report, COVID-19 (recurred Covid 19) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 11-May-2021, SARS-CoV-2 test: positive (Positive) Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient received other unspecified medications/products within 2 weeks of starting COVID-19 treatment. After 4 days completing Paxlovid, symptoms of nasal congestion and generalized achiness recurred. Patient had been symptomatic for 3 days after developing Covid 19 on 11-May-2022. Symptoms were nasal congestion and achiness and diagnosis made by rapid Ag test. patient began Paxlovid on 13-May-2022 and was symptom free by 16-May-2022. The COVID-19 recurred again on 20-May-2022 at 17:30. The device date was 21-May-2022. Company comment: This is a spontaneous case concerning a 71-year-old male patient, with no relevant medical history, who experienced the unexpected, non-serious AESI of COVID-19 (reported as recurred Covid 19), approximately 7 months after the third dose of mRNA-1273 vaccine. No details of previous doses were provided. As per source document, he received Paxlovid as treatment and 4 days after completed it, symptoms of nasal congestion and generalized achiness recurred. A positive SARS-CoV-2 was performed. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This is a spontaneous case concerning a 71-year-old male patient, with no relevant medical history, who experienced the unexpected, non-serious AESI of COVID-19 (reported as recurred Covid 19), approximately 7 months after the third dose of mRNA-1273 vaccine. No details of previous doses were provided. As per source document, he received Paxlovid as treatment and 4 days after completed it, symptoms of nasal congestion and generalized achiness recurred. A positive SARS-CoV-2 was performed. 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: 20210511; Test Name: COVID-19 virus test; Test Result: Positive ; Result Unstructured Data: Positive
Aktuelle Erkrankungen: Asthma
Vorgeschichte: -
Andere Medikamente: LIPITOR; LAMISIL [TERBINAFINE HYDROCHLORIDE]
Allergien: -
Vorherige Impfungen: -

VAERS 2293359

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: 41,0
Geschlecht: F
Eingang: 25.05.2022
Impfdatum: 15.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 16,0
Dosis: 3
Route/Site: - / LA

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

Heavy menstrual bleeding

Symptomtext

I rarely got my period anymore, but then 2 weeks after the vaccine, I had my period for almost 2 full months.

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Praegender Schweregrund: Heavy menstrual bleeding
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: None
Andere Medikamente: Birth Control
Allergien: None
Vorherige Impfungen: -

VAERS 2278839

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MA
Alter: 52,0
Geschlecht: F
Eingang: 16.05.2022
Impfdatum: 12.04.2021
Beginn: 12.04.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: - / -

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

COVID-19 Cognitive disorder Magnetic resonance imaging Neuropsychological test

Symptomtext

Patient felt she developed recurrence of fluctuating cognitive impairment that accompanied Covid infection. Developed over 2-3 weeks after each of her 3 vaccines (2 Pfizer and 1 Moderna)

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: MRI pending Neuropsych pending
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: Prasterone, DHEA, (DHEA) 25 mg capsule Thyroid, Pork, (ARMOUR THYROID) 60 mg tablet multivitamin (MULTI-DAY ORAL) levocarnitine (L-CARNITINE ORAL) COQ10, LIPOSOMAL UBIQUINOL, ORAL vit B complex no.12/niacin,B3, (VITAMIN B COMPLEX NO.12
Allergien: Alupent [Metaproterenol] Not Specified 7/30/2006 Past Updates... Cleocin [Clindamycin] Not Specified 7/24/2006 Past Updates... Marax [Ephedrine Hemihydrate] Not Specified 8/23/2014 Past Updates... Penicillin [Penicillins]
Vorherige Impfungen: -

VAERS 2270840

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: 64,0
Geschlecht: F
Eingang: 11.05.2022
Impfdatum: 17.03.2021
Beginn: 28.02.2022
Tage bis Beginn: 348,0
Dosis: UNK
Route/Site: - / -

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

Acute kidney injury COVID-19 SARS-CoV-2 test positive

Symptomtext

02/28/22 presents to ED for "AKI". PMHx of "atrial fib s/p PPM/ICD, 1 kidney after donating a kidney to family member ~40 years ago"

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acute kidney injury
Hospital-Tage: -
Labordaten: 02/28/22 SARS-CoV-2 (COVID-19) by NAA detected
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2264792

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: OH
Alter: 49,0
Geschlecht: F
Eingang: 05.05.2022
Impfdatum: 26.11.2021
Beginn: 27.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / RA

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

Immunisation reaction

Symptomtext

COVID ARM

Weitere VAERSDATA-Felder

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

VAERS 2259790

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: NC
Alter: 61,0
Geschlecht: F
Eingang: 30.04.2022
Impfdatum: 01.11.2021
Beginn: 01.12.2021
Tage bis Beginn: 30,0
Dosis: 3
Route/Site: SYR / RA

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

Alopecia Gingival swelling Impaired work ability Lymphadenopathy Tongue blistering

Symptomtext

(My first 2 shots were Pfizer.) I don't absolutely know if these are vaccine-related events, but I know people who have been losing their hair since they had the shots. My hair suddenly started thinning, and it's still happening after 5 months. I also have a few blisters in my mouth (on my tongue) and swelling in my gums that come and go. I've seen both of these things being reported online, which made me want to report them here. Lastly, I still have a bit of lymph swelling under my arms. I tend to take very good care of myself so these are strange symptoms for me. I also want to say that I had very strong and painful reactions to the last 2 shots. My doctor said it was good because it means I have a "strong immune system," but I honestly don't know how the makers of these vaccines don't take into account the pain that some of us suffer after the vaccines. I was out of work for a week...and they want us to keep boosting? I'm all for helping my fellow person, but it's not a small deal to suffer through these vaccines and be told: "most symptoms are mild." Just not the case for SO MANY of us! This is also a reason why there are many who don't want to get the vaccine. (I've traveled out of the country and have had to have a lot of vaccines in my life. I've had strong vaccine reactions before, but none like these vaccines, FYI.)

Weitere VAERSDATA-Felder

Praegender Schweregrund: Alopecia
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: It's possible I have an auto-immune disorder but nothing diagnosed. I'm historically highly sensitive to vaccines, medication, etc.
Andere Medikamente: Multivitamin, probiotic, vitamin d, trace minerals
Allergien: Shrimp, aspirin, codeine, Tylenol, amoxicillin, sulfur, hay, pollen
Vorherige Impfungen: -

VAERS 2248073

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: CA
Alter: 67,0
Geschlecht: M
Eingang: 22.04.2022
Impfdatum: 02.11.2021
Beginn: 02.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Shoulder injury related to vaccine administration

Symptomtext

SIRVA; symptom onset after vaccine, worsening with time. First sought treatment in our office today.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Shoulder injury related to vaccine administration
Hospital-Tage: -
Labordaten: NA. Referred to physical therapy and to sports medicine for cortisone injection.
Aktuelle Erkrankungen: none
Vorgeschichte: hypertension depression
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 2247901

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: SC
Alter: 59,0
Geschlecht: F
Eingang: 22.04.2022
Impfdatum: 04.12.2021
Beginn: 01.02.2022
Tage bis Beginn: 59,0
Dosis: 3
Route/Site: IM / RA

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

Tinnitus

Symptomtext

I started getting a buzzing in both ears. It was getting worse and louder. It is constant but the loudness varies. I told my doctor and he did not have any suggestions for the tinnitus. I did try to plug my nose and blow and it seems to make it worse. It still continues to this day.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: None
Vorgeschichte: Seasonal allergies; hypothyroidism
Andere Medikamente: Fish oil; multivitamin; vitamin B3; vitamin complex; calcium
Allergien: None
Vorherige Impfungen: -

VAERS 2241704

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MT
Alter: 78,0
Geschlecht: F
Eingang: 19.04.2022
Impfdatum: 02.12.2021
Beginn: 05.04.2022
Tage bis Beginn: 124,0
Dosis: 3
Route/Site: IM / UN

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

COVID-19

Symptomtext

Diagnosed and hospitalized with COVID while up to date with vaccinations

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: 4,0
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2218150

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MA
Alter: 65,0
Geschlecht: F
Eingang: 06.04.2022
Impfdatum: 01.03.2021
Beginn: 01.05.2021
Tage bis Beginn: 61,0
Dosis: 3
Route/Site: IM / RA

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

Muscle spasms Tinnitus

Symptomtext

After the first vaccine I started to have regular muscle spasms in my left arm. After the second dose I noticed constant ringing in my ears and it has not gone away. I tried two OTC remedies without success and I am now taking Zoloft which has not helped.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Muscle spasms
Hospital-Tage: -
Labordaten: Hearing test.
Aktuelle Erkrankungen: None
Vorgeschichte: Osteopenia
Andere Medikamente: Vitamin D
Allergien: NKA
Vorherige Impfungen: -

VAERS 2214065

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: NJ
Alter: 29,0
Geschlecht: M
Eingang: 04.04.2022
Impfdatum: 20.11.2021
Beginn: 22.11.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: SYR / LA

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

Acoustic stimulation tests abnormal Deafness unilateral Magnetic resonance imaging normal Tinnitus

Symptomtext

Tinnitus of right ear and hearing loss after waking up about 2 days after the shot. Tinnitus became permanent every second 24/7 on right ear. As days and weeks went by, tinnitus of left ear developed as well and the right ear's hearing loss became severe. Saw ENT doctors and both diagnosed tinnitus and hearing loss after audiology hearing tests. Prescribed 2 weeks of Prednisone tablets, but no effect. Till this day (today is 4/4/2022), hearing loss and tinnitus remains with no improvement at all based on the follow up audiology tests. MRI scan performed and ruled out tumors or cancer.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acoustic stimulation tests abnormal
Hospital-Tage: -
Labordaten: Audiology tests on: 12/7/2021, 1/24/2022, 3/10/2022 MRI on: 2/9/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2199613

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: CA
Alter: 15,0
Geschlecht: M
Eingang: 25.03.2022
Impfdatum: 07.12.2021
Beginn: 07.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Product administered to patient of inappropriate age

Symptomtext

Patient received 2 doses of a manufacturer unknown COVID-19 vaccine. Patient requested a Moderna booster (0.25mL); administered to the patient on 12/7/2021. However, patient was 15 years old (<18 years old) at the time of vaccination, and should not have received a dose of Modera (would have only been eligible for Pfizer vaccine). School nurse was informed of the incident and will inform the patient and his parents.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: N/A.
Aktuelle Erkrankungen: Unknown
Vorgeschichte: Unknown
Andere Medikamente: Unknown
Allergien: Unknown
Vorherige Impfungen: -

VAERS 2167678

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 09.03.2022
Impfdatum: 10.01.2022
Beginn: 10.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided Treatment medication was not provided by the reporter The vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. On 1-Dec-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165122

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 14.01.2022
Beginn: 14.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temperature, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temperature, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temperature, re-frozen at ti me of arrival). At the time of the report, PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temperature, re-frozen at ti me of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided by the reporter. No treatment was provided by the reporter. This case was linked to MOD-2022-496015 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165120

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
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 Product temperature excursion issue

Symptomtext

Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.; Total duration of the excursion refrigerated temps for max of 4 hrs.; They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs.) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 04-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs.) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information was provided. No treatment medication were provided. It was reported that total duration of the excursion refrigerated temperature for maximum of 4 hour. On 01-Dec-2021 Vial was moved to fridge. State of the vaccine at the time of excursion was partially thawed/liquid. This case was linked to MOD-2022-496015 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165117

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival/ Total duration of the excursion refrigerated temps for max of 4 hrs; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival/ Total duration of the excursion refrigerated temps for max of 4 hrs) and EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 21-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival/ Total duration of the excursion refrigerated temps for max of 4 hrs). At the time of the report, PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival/ Total duration of the excursion refrigerated temps for max of 4 hrs) and EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Treatment information was not provided. The vial was moved to the fridge on 01-Dec-2021 and administered post 30 days. The facility thought that the vials were received frozen from Moderna, so they have been unpacking them and putting them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. This case was linked to MOD-2022-496015 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165107

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 04-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) 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 01-Dec-2021 Vial was moved to fridge. State of the vaccine at the time of excursion was partially thawed/liquid. The maximum or minimum temperature reached by the vial was 8 degree Celsius. Total duration of the excursion refrigerated temperature for maximum of 4 hour reported by Reporter. It was reported that the vials were re-frozen. Temperature fluctuations had occurred from frozen state to refrigerated state to being re-frozen.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165105

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 10.01.2022
Beginn: 10.01.2022
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 Product temperature excursion issue

Symptomtext

Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.; Total duration of the excursion refrigerated temps for max of 4 hrs.; They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs.) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).), PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at the time of arrival.) and PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. It was unknown if the vial was undergone a previous temperature excursion. The storage condition at the time of the excursion was frozen storage/refrigerated storage. The state of the vaccine at the time of the excursion was partially thawed/liquid. The maximum temperature reached was 8?C. the total duration of the excursion refrigerated temps for max of 4 hours. The temperature fluctuations occurred as frozen-refrigerated and refrozen. It was also reported that on 01-Dec-2021, the vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2?C to 8?C. 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 2165101

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 04-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that on 1-Dec-2021 vaccine was moved to fridge and vaccine administrered post 30 days from the initial storage at 2C to 8C. No concomitant were reported. No treatment were reported. This case was linked to MOD-2022-496015.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165093

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 25.01.2022
Beginn: 25.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product use was reported. It was unknown if the vial was undergone a previous temperature excursion. The storage condition at the time of the excursion was frozen storage refrigerated storage. The state of the vaccine at the time of the excursion was partially thawed liquid. The maximum temperature reached was 8 degree celsius. the total duration of the excursion refrigerated temps for max of 4 hours. The temperature fluctuations occurred as frozen-refrigerated and refrozen. It was also reported that on 01-Dec-2021, the vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2 degree Celsius to 8 degree Celsius. No treatment information was provided. This case was linked to MOD-2022-501713 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165089

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 18.01.2022
Beginn: 18.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 18-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) 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. The facility thought that the vials were received frozen from Moderna, so they have been unpacking them and putting them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. On 01-Dec-2021 vaccine was moved to fridge and vaccine administration post 30 days from the initial storage at 2C to 8C.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165087

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 04.01.2022
Beginn: 04.01.2022
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 Product temperature excursion issue

Symptomtext

This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 04-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. The facility thought that the vials were received frozen from Moderna, so they have been unpacking them and putting them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. Vial was moved to fridge on 01 Dec 2021 and vaccine was administered past 30 days from the initial storage at 2 degree Celsius to 8 degree Celsius. Temperature was fluctuated Frozen-refrigerated and again refrozen. Frozen vails removed and transported refrigerated temperature and refrozen at time of arrival. Total duration of excursion refrigerated temperature for max 4 hours. Temperature reached to 8 degrees Celsius. Vials size was 5.5 ml and 7.5 ml. Partially thawed liquid state at the time of excursion. No treatment medications were reported. This case was linked to MOD-2022-496015 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165086

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 25.01.2022
Beginn: 25.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The patient MRN Number was reported No concomitant medication information was provided. The vial was moved to fridge on 01-dec-2021. Total duration of the excursion refrigerated temperature for maximum 4 hours No treatment medication information was given.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165085

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 13.01.2022
Beginn: 13.01.2022
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Expired product administered Product storage error Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 13-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No treatment medication was reported. No concomitant medication was reported. Vial was moved to fridge on 01-Dec-21. Vaccine was administered past the 30-day from the initial storage at 2 degree Celsius to 8 degree Celsius.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165083

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 25.01.2022
Beginn: 25.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen / They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen / They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen / They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen / They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen / They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen / They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen / They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen / They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided Patient ID reported. The vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. On 1-Dec-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C. 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 2165082

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 07-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Patient MRN id reported as 6004898. No concomitant medications were reported. It was unknown if the vial was undergone a previous temperature excursion. The storage condition at the time of the excursion was frozen storage/refrigerated storage. The state of the vaccine at the time of the excursion was partially thawed/liquid. The maximum temperature reached was 8?C. the total duration of the excursion refrigerated temps for max of 4 hours. The temperature fluctuations occurred as frozen-refrigerated and refrozen. It was also reported that on 01-Dec-2021, the vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2?C to 8?C. No treatment medications were reported. This case was linked to MOD-2022-496015 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165080

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) 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 vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. On 1-Dec-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C. 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 2165074

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
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 Product temperature excursion issue

Symptomtext

They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).; Total duration of the excursion refrigerated temps for max of 4 hrs; They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).), PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) and EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Jan-2022, the patient experienced PRODUCT STORAGE ERROR (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).), PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) and EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).). At the time of the report, PRODUCT STORAGE ERROR (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).), PRODUCT TEMPERATURE EXCURSION ISSUE (Total duration of the excursion refrigerated temps for max of 4 hrs) and EXPIRED PRODUCT ADMINISTERED (They have been accidentally administering refrozen vials to their patients (more than 30 days after moving to fridge).) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication details was reported. The vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. No treatment medication details was reported. The vial was moved to fridge on 01-Dec-2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2165073

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment details were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2164999

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) 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 vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. On 1-Dec-2021 vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C. No treatment medications were reported. MRN ID-00451624

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2164998

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. The vial was moved to fridge on 01-Dec-2021. No concomitant medications were reported. It was reported that there was no product complaint associated. No treatment medications were reported. This case was linked to MOD-2022-496015 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2164991

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
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

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 07-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT STORAGE ERROR (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication details was reported. The vials were frozen, shipped in refrigerated temperature and then refroze for storage once arrive at facility. No treatment medication details was reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2164987

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 06.01.2022
Beginn: 06.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 06-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) 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 information was reported. The facility thought that the vials were received frozen from Moderna, so they have been unpacking them and putting them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients.The vial was moved to the fridge on 01-Dec-2021 and administered post 30 days from the initial storage at 2C to 8C. This case was linked to MOD-2022-496015 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2164986

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 21.01.2022
Beginn: 21.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 21-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 21-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. Not Provided The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant and treatment medications were reported. Vial moved to fridge on 01-DEC-2021. Total duration of the excursion refrigerated temperature for maximum 4 hours.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2164985

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 10.01.2022
Beginn: 10.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) 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 facility thought that the vials were received frozen from Moderna, so they have been unpacking them and putting them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. On 1 Dec 2021 vaccine was moved to fridge and vaccine administrered post 30 days from the initial storage at 2C to 8C. The treatment information was unknown. This case was linked to MOD-2022-496015 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2164984

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 08.03.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
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 Product temperature excursion issue

Symptomtext

This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. On 1-Dec-2021, vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2C to 8C. 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 2162293

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 07.03.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at time of arrival) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment details were reported.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2162292

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 07.03.2022
Impfdatum: 11.01.2022
Beginn: 11.01.2022
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 Product temperature excursion issue

Symptomtext

Found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials; Frozen vials, removed and transported at refrigerated temperature, re-frozen at time of arrival; Accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (Found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temperature, re-frozen at time of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temperature, re-frozen at time of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (Found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temperature, re-frozen at time of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product information was not provided Total duration of the excursion refrigerated temperature for maximum of 4 hour. On 01Dec2021 Vial was moved to fridge. The facility thought that the vials are received frozen from Moderna so they had unpacked them and put them back into the facility freezer. They just recently found out that the vials are received in refrigerated temperatures and not frozen. They have been accidentally administering refrozen vials to their patients. Vaccine administered post 30 days from the initial storage at 2 degree C to 8 degree C 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 2160954

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: IL
Alter: -
Geschlecht: U
Eingang: 05.03.2022
Impfdatum: 07.01.2022
Beginn: 07.01.2022
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 Product temperature excursion issue

Symptomtext

They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival; They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 07-Jan-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Jan-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival). At the time of the report, EXPIRED PRODUCT ADMINISTERED (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients), PRODUCT STORAGE ERROR (They just recently found out that the vials are received in refrigerated temperatures and not frozen/ They have been accidentally administering refrozen vials to their patients) and PRODUCT TEMPERATURE EXCURSION ISSUE (Frozen vials, removed and transported at refrigerated temp, re-frozen at ti me of arrival) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. It was unknown if the vial was undergone a previous temperature excursion. The storage condition at the time of the excursion was frozen storage/refrigerated storage. The state of the vaccine at the time of the excursion was partially thawed/liquid. The maximum temperature reached was 8?C. the total duration of the excursion refrigerated temps for max of 4 hours. The temperature fluctuations occurred as frozen-refrigerated and refrozen. It was also reported that on 01-Dec-2021, the vaccine was moved to fridge and vaccine administered post 30 days from the initial storage at 2?C to 8?C. No treatment information was provided. This case was linked to MOD-2022-496015 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2155089

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MN
Alter: 50,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 03.04.2021
Beginn: 02.03.2022
Tage bis Beginn: 333,0
Dosis: 3
Route/Site: IM / -

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

Unevaluable event

Symptomtext

11/5/2021-dose #3 Lot Number 033F21A

Weitere VAERSDATA-Felder

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

VAERS 2154638

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MA
Alter: 62,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 12.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Tinnitus

Symptomtext

AFTER RECEIVING MODERNA BOOSTER SHOT. TINNITUS. NO TREATMENT. CONSTANT RINGING/BUZZING.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Tinnitus
Hospital-Tage: -
Labordaten: NONE
Aktuelle Erkrankungen: NONE
Vorgeschichte: HIGH BLOOD PRESSURE, HIGH CHOLESTEROL, GLAUCOMA, DEPRESSION
Andere Medikamente: LISINOPRIL, VENLAFAXINE, SIMVASTATIN, VITAMIN D, CALCIUM SUPPLEMENT, TIMOLOL MALEATE (EYE DROPS), BRIMONIDINE (EYE DROPS), LATANOPROST (EYE DROPS)
Allergien: NONE
Vorherige Impfungen: -

VAERS 2154626

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: 70,0
Geschlecht: F
Eingang: 03.03.2022
Impfdatum: 23.01.2021
Beginn: 01.08.2021
Tage bis Beginn: 190,0
Dosis: 1
Route/Site: IM / RA

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

Acoustic stimulation tests abnormal Deafness unilateral Discomfort Hearing aid therapy Hypoacusis Magnetic resonance imaging normal Scan with contrast normal

Symptomtext

Was having trouble not hearing especially when I attended church services. Also was noticing that certain voices on the television were distorted or uncomfortable to listen to.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Acoustic stimulation tests abnormal
Hospital-Tage: -
Labordaten: Went to the audiologist for a hearing test. Was also seen by the ENT doctor to make sure that there were no blockages. Was sent for an MRI with and without contrast. Results of the MRI was that everything looked normal. Returned to the Advanced ENT Specialists for a second hearing test. Results were different from just a few months before. Only lost hearing in my right ear. I have recently received a hearing aid for assistance.
Aktuelle Erkrankungen: none
Vorgeschichte: hypothyroidism
Andere Medikamente: Synthroid 0.075 mg, Vitamin D3
Allergien: Catfish - food, penicillium - joint swell
Vorherige Impfungen: -

VAERS 2150643

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: 45,0
Geschlecht: F
Eingang: 01.03.2022
Impfdatum: 10.04.2021
Beginn: 31.01.2022
Tage bis Beginn: 296,0
Dosis: 2
Route/Site: OT / -

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

COVID-19 Ear discomfort Interchange of vaccine products SARS-CoV-2 test

Symptomtext

Interchange of vaccine products (1st dose of Janssen COVID-19 Vaccine and 2nd dose of Moderna); Covid-19 infection; Congestion in ear clogged; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (Covid-19 infection), EAR DISCOMFORT (Congestion in ear clogged) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products (1st dose of Janssen COVID-19 Vaccine and 2nd dose of Moderna)) in a 45-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for Prophylactic vaccination. Co-suspect product included non-company product COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) for Prophylactic vaccination. No Medical History information was reported. On 10-Apr-2021, the patient received first dose of COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) (unknown route) 1 dosage form. On 03-Dec-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 31-Jan-2022, the patient experienced COVID-19 (Covid-19 infection) and EAR DISCOMFORT (Congestion in ear clogged). On an unknown date, the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products (1st dose of Janssen COVID-19 Vaccine and 2nd dose of Moderna)). At the time of the report, COVID-19 (Covid-19 infection) was resolving and EAR DISCOMFORT (Congestion in ear clogged) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products (1st dose of Janssen COVID-19 Vaccine and 2nd dose of Moderna)) outcome was unknown. Not Provided DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 31-Jan-2022, SARS-CoV-2 test: positive (Positive) Positive. No treatment details reported. Company comment: This case concerns a 45 year old female patient with prior vaccination with COVID-19 vaccine NRVV AD26, who experienced the unexpected non serious AESI event of Covid 19 1 month 28 days after receiving a dose of mRNA-1273 Vaccine. Current pandemic of Covid 19 can be a risk factor. Covid 19 rapid test was reported to be positive. Interchange of vaccine products also noted in the case. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This case concerns a 45 year old female patient with prior vaccination with COVID-19 vaccine NRVV AD26, who experienced the unexpected non serious AESI event of Covid 19 1 month 28 days after receiving a dose of mRNA-1273 Vaccine. Current pandemic of Covid 19 can be a risk factor. Covid 19 rapid test was reported to be positive. Interchange of vaccine products also noted in the case. 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: 20220131; Test Name: COVID-19 Rapid test; Test Result: Positive ; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2137004

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: 64,0
Geschlecht: M
Eingang: 24.02.2022
Impfdatum: 22.11.2021
Beginn: 23.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / UN

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

Mouth ulceration

Symptomtext

I had a mouth ulcer a day after vaccine, It stayed a day or 2. I went to see my doctor, which he prescribed me some Valtrex. It took at least 3 weeks until I seen a difference.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Mouth ulceration
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: None
Vorgeschichte: Sleep insomnia High Cholesterol
Andere Medikamente: Crestor 40MG Zetia 10MG Aspirin 81MG Trelegy Fish oil Multi-Vitamins Zyrtec Coq-10
Allergien: Dextromethorphan Singulair
Vorherige Impfungen: -

VAERS 2115700

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Product administration error Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet; Vaccine administered after temperature excursion; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion), PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) and PRODUCT ADMINISTRATION ERROR (Vaccine administered after temperature excursion) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion), PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) and PRODUCT ADMINISTRATION ERROR (Vaccine administered after temperature excursion). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion), PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) and PRODUCT ADMINISTRATION ERROR (Vaccine administered after temperature excursion) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant medications were reported No treatments were reported It was reported that total 19 patients received expired vaccine out of which 3 were males and 16 were females. It was reported that 10 vials of 15 doses each were stored in a freezer whose temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit. The healthcare provider mentioned that they always had the freezer between this temperature range. Two vials were used to administer to healthcare provider's office employees. All doses were injected intramuscularly in deltoid muscle. Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. In follow-up the reporter informed that, the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt.. The patient did not experience any adverse events after receiving the booster dose of vaccine and the healthcare provider was informed that the vaccine could be used until the date of expiration. Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Follow up received updated narrative

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administration error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115699

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were provided. 10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree F to 24.7 degree F. All doses were injected IM in deltoid muscle. Administration date: 23 Nov 2021 and 27 Nov2021. The reporter stated that While the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt, they have not had any adverse events. Moderna has stated vaccine could continued to be used until expiration. No treatment medication were provided. Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Follow up document received on 10-Feb-2022 contains significant information, Confirmed that Not experienced any Adverse events.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115698

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication was reported. Reporter stated that 10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F. HCP mentioned that they always had the freezer between this range. Two vials were used to administered HCP's office employees. All doses were injected IM in deltoid muscle. Lot #033F21A. Exp. Date 08Apr2022. Upon follow up it was reported that vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt and did not had any adverse events. Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. Further it was reported that vaccine could be used until expiration date. Treatment medication was not provided by the reporter. This case was linked to MOD-2022-474544 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Follow up received contains Significant information-updated narrative

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115697

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F; This spontaneous case was reported by a health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications was provided by the reporter. No treatment medications was provided by the reporter. It was reported that total 19 patients received expired vaccine out of which 3 were males and 16 were females. It was reported that 10 vials out of 15 doses each were stored in a freezer whose temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit. The healthcare provider mentioned that they always had the freezer between this temperature range. Two vials were used to administer to healthcare provider's office employees. All doses were injected intramuscularly in deltoid muscle. Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. The reporter informed that, the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt.. The patient did not experience any adverse events after receiving the booster dose of vaccine and the healthcare provider was informed that the vaccine could be used until the date of expiration. Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Follow-up received contain significant information outcome of the event of product storage error and narrative updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115696

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit; Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit). In November 2021, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit) had resolved. At the time of the report, PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment information was provided. It was reported that total 19 patients received the affected lot of vaccine out of which 3 were males and 16 were females. 2 second doses (both given to female patients) and 17 booster doses were given to the patients. The healthcare provider mentioned that they always had the freezer between this temperature range from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit. Two vials were used to administer to healthcare provider's office employees. All doses were injected in deltoid muscle. Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. The reporter informed that, the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt. The patient did not experience any adverse events after receiving the vaccine and the healthcare provider was informed that the vaccine could be used until the date of expiration. This case was linked to MOD-2022-474599, MOD-2022-479778, MOD-2022-479873, MOD-2022-479908, MOD-2022-479943, MOD-2022-479957, MOD-2022-479962, MOD-2022-479969, MOD-2022-479975, MOD-2022-479978, MOD-2022-479984, MOD-2022-479989, MOD-2022-479991, MOD-2022-479997, MOD-2022-479999, MOD-2022-480005, MOD-2022-480007, MOD-2022-474544 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Significant Follow up received: contains narrative updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115695

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) 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 given. It was reported that 10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit. HCP mentioned that they always had the freezer between this range. All doses were injected IM in deltoid muscle. It was reported that the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt, and they have not had any adverse events. Moderna has stated vaccine could continued to be used until expiration. Storage condition at the time of the excursion was frozen storage. Maximum temperatures reached, as applicable was Maximum of 24.7 degree Fahrenheit. Excursion duration was from 09Nov2021 to current date (vials have not been moved from freezer). Currently vials were stored in freezer. Visual inspection noting any vaccine state change was visually inspected frozen (never been thawed). Proposed desired Use by Date (date of vaccination clinic, patient appointments, etc. that HCP would like vaccine administered from the vials in question) was unknown. Number of vials/doses impacted were 10 15-dose vials. Pertinent details like whether the vial(s) were punctured, any previous excursions with the impacted vial(s) include no other excursions. Two vials were used. Doses were administered on 23Nov2021 and 27Nov2021 Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Follow up received contains information on product storage error and added to I narrative supplement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115694

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. The concomitant medications on use were not provided. It was reported that total 19 patients received expired vaccine out of which 3 were males and 16 were females. It was reported that 10 vials out of 15 doses each were stored in a freezer whose temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit. The healthcare provider mentioned that they always had the freezer between this temperature range. Two vials were used to administer to healthcare provider's office employees. All doses were injected intramuscularly in deltoid muscle. Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. The reporter informed that, the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt. The patient did not experienced any adverse events after receiving the vaccine and the healthcare provider was informed that the vaccine could be used until the date of expiration. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Updated narrative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115693

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: M
Eingang: 16.02.2022
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 Product storage error

Symptomtext

Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet; Expired Vaccine administered; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) and EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) and EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered). At the time of the report, PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) and EXPIRED PRODUCT ADMINISTERED (Expired Vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Concomitant medication information was not provided. Treatment information was not provided. This case was linked to MOD-2022-474599 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Follow Up received on 10-FEB-2022 Contains Significant information: Updated Outcome of the events

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115692

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant products were reported. No treatment drugs were reported It was reported that total 19 patients received expired vaccine out of which 3 were males and 16 were females. It was reported that 10 vials out of 15 doses each were stored in a freezer whose temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit. The healthcare provider mentioned that they always had the freezer between this temperature range. Two vials were used to administer to healthcare provider's office employees. All doses were injected intramuscularly in deltoid muscle. Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. The reporter informed that, the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt.. The patient did not experience any adverse events after receiving vaccine and the healthcare provider was informed that the vaccine could be used until the date of expiration. Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Follow-up received as additional information to initial version and I-narrative supplement updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115691

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree Fahrenheit; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree Fahrenheit) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree Fahrenheit). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree Fahrenheit) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant products were reported. It was reported that total 19 patients received expired vaccine out of which 3 were males and 16 were females. It was reported that 10 vials out of 15 doses each were stored in a freezer whose temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit. The healthcare provider mentioned that they always had the freezer between this temperature range. Two vials were used to administer to healthcare provider's office employees. All doses were injected intramuscularly in deltoid muscle. Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. The reporter informed that, the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt. The patient did not experience any adverse events after receiving the booster dose of vaccine and the healthcare provider was informed that the vaccine could be used until the date of expiration. No treatment drugs were reported. This case was linked to MOD-2022-474599, MOD-2022-479993, MOD-2022-479969 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Follow-up received contain significant information: narrative and date of vaccination were updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115690

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit; Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit). In November 2021, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit) had resolved. At the time of the report, PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. It was reported that total 19 patients received the affected lot of vaccine out of which 3 were males and 16 were females. 2 second doses (both given to female patients) and 17 booster doses were given to the patients. The healthcare provider mentioned that they always had the freezer between this temperature range from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit. Two vials were used to administer to healthcare provider's office employees. All doses were injected in deltoid muscle. Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. The reporter informed that, the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt. The patient did not experience any adverse events after receiving the vaccine and the healthcare provider was informed that the vaccine could be used until the date of expiration. This case was linked to MOD-2022-474599, MOD-2022-474544, MOD-2022-479778, MOD-2022-479873, MOD-2022-479908, MOD-2022-479943, MOD-2022-479957, MOD-2022-479962, MOD-2022-479975, MOD-2022-479978, MOD-2022-479984, MOD-2022-479989, MOD-2022-479991, MOD-2022-479993, MOD-2022-479997, MOD-2022-479999, MOD-2022-480005, MOD-2022-480007 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Significant Follow up received: contains updated outcome of the event of product storage error and narrative updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115689

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications was provided by the reporter. It was reported that total 19 patients received expired vaccine out of which 3 were males and 16 were females. It was reported that 10 vials out of 15 doses each were stored in a freezer whose temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit. The healthcare provider mentioned that they always had the freezer between this temperature range. Two vials were used to administer to healthcare provider's office employees. All doses were injected intramuscularly in deltoid muscle. Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. The reporter informed that, the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt.. The patient did not experience any adverse events after receiving vaccine and the healthcare provider was informed that the vaccine could be used until the date of expiration. No treatment medications was provided by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Follow-up received as additional information to initial version and I-narrative supplement updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115688

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant medication information was reported. No Treatment medications were provided Excursion duration: From 09Nov2021 to current date.There are total of 10 15-dose vials were impacted. The HCP mentioned that they always had the freezer between this temperature range. Two vials were used to administer to healthcare provider's office employees. Anatomical location was reported as Deltoid muscle Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. The reporter informed that, the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt. Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Follow up document contains updated the event verbatim and I narrative supplement.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115687

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet; This spontaneous case was reported by a health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant products were reported. No treatment drugs were reported It was reported that total 19 patients received expired vaccine out of which 3 were males and 16 were females. It was reported that 10 vials out of 15 doses each were stored in a freezer whose temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit. The healthcare provider mentioned that they always had the freezer between this temperature range. Two vials were used to administer to healthcare provider's office employees. All doses were injected intramuscularly in deltoid muscle. Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. The reporter informed that, the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt. The patient did not experience any adverse events after receiving the booster dose of vaccine and the healthcare provider was informed that the vaccine could be used until the date of expiration. Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: On 10-Feb-2022: Follow-up received contain significant information outcome of the event of product storage error and narrative updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115685

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet; Vaccine administered after temperature excursion; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree Fahrenheit) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet). In November 2021, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) had resolved. At the time of the report, PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. It was reported that 10 vials of 15 doses each were stored in a freezer of which the temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit. The reporter stated that they always had the freezer between the 24.3 degree Fahrenheit to 24.7 degree Fahrenheit temperature range. The storage condition at the time of excursion was reported as Frozen storage. The maximum temperature reached was reported as Maximum of 24.7 degree Fahrenheit. Excursion duration was reported as from 09-Nov-2021 to current date (vials have not been removed from freezer). It was reported that the vials are stored in the freezer. The vials had never been thawed. The proposed desired Use by Date was unknown. 10 vials of 15 doses were impacted. It was reported that 2 vials were used and the doses were administered on 23-Nov-2021 and 27-Nov-2021. It was stated that two vial's were used to administer HCP's office employees. It was also reported that all doses were injected intramuscular in deltoid muscle. It was reported that 19 patients were involved of which 3 were males and 16 were females. It was reported that 2 second doses were given (both given to female patients) and 17 boosters were given. Administration date was reported 23-Nov-2021 and 27-Nov-2021. Reporter stated that while the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt, they have not had any adverse events. This case was linked to MOD-2022-474599, MOD-2022-479993 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: I-narrative updated

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115684

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F). In November 2021, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) had resolved. At the time of the report, PRODUCT STORAGE ERROR (stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication reported. No treatment medication reported. It was reported that 10 vials out of 15 doses each were stored in a freezer whose temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit. The healthcare provider mentioned that they always had the freezer between this temperature range. Two vials were used to administer to healthcare provider's office employees. All doses were injected intramuscularly in deltoid muscle. Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. The vaccine was administered after been frozen at 23 degrees Fahrenheit since receipt. The patient did not experience any adverse events after receiving the booster dose of vaccine and the healthcare provider was informed that the vaccine could be used until the date of expiration. This case was linked to MOD-2022-474544 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Significant Follow up received, contains updated narrative.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115682

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: M
Eingang: 16.02.2022
Impfdatum: 01.11.2021
Beginn: 01.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. In November 2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. In November 2021, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/ vaccine administered after being frozen at 23 degree fahrenhiet) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication reported. No treatment medication reported. It was reported that 10 vials out of 15 doses each were stored in a freezer whose temperature range was at all times from 24.3 degree Fahrenheit to 24.7 degree Fahrenheit. The healthcare provider mentioned that they always had the freezer between this temperature range. Two vials were used to administer to healthcare provider's office employees. All doses were injected intramuscularly in deltoid muscle. The reporter informed that, the vaccine was administered after being frozen at 23 degrees Fahrenheit since receipt. Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. The patient did not experience any adverse events after receiving the booster dose of vaccine and the healthcare provider was informed that the vaccine could be used until the date of expiration. Most recent FOLLOW-UP information incorporated above includes: On 10-Feb-2022: Significant Follow up received: contains updated outcome of the event of product storage error and narrative updated.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2115609

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: NJ
Alter: 45,0
Geschlecht: F
Eingang: 16.02.2022
Impfdatum: 03.12.2021
Beginn: 31.01.2022
Tage bis Beginn: 59,0
Dosis: 2
Route/Site: OT / -

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

COVID-19 Ear discomfort SARS-CoV-2 test

Symptomtext

COVID-19 INFECTION; CONGESTION IN EAR CLOGGED; This spontaneous report received from a patient concerned a 45 year old female. The patient's height, and weight were not reported. No past medical history or concurrent conditions were reported. The patient received covid-19 vaccine ad26.cov2.s (dose number in series:1) (suspension for injection, route of admin not reported, batch number: 203A21A, expiry: UNKNOWN) dose was not reported, 1 total administered on 10-APR-2021 on left arm for prophylactic vaccination. No adverse events were reported following covid-19 vaccine ad26.cov2.s (Dose number in series: 1) Non-company suspect vaccine included: mrna 1273 ( Moderna) (dose number in series:2) ( batch number: 033F21A expiry: UNKNOWN, form of admin, route of admin, and were not reported) dose was not reported, administered on 03-DEC-2021 for prophylactic vaccination. No concomitant medications were reported. On 31-JAN-2022, the patient experienced covid-19 infection, using the binax home rapid antigen test and congestion in ear clogged (dose number in series:2). Laboratory data included: COVID-19 rapid POC test (NR: not provided) Positive. The action taken with covid-19 vaccine ad26.cov2.s was not applicable. The patient was recovering from covid-19 infection, and the outcome of congestion in ear clogged was not reported. This report was non-serious.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: Test Date: 20220131; Test Name: COVID-19 rapid POC test; Result Unstructured Data: Positive
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2104404

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: OH
Alter: 66,0
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: 11.01.2022
Beginn: 08.02.2022
Tage bis Beginn: 28,0
Dosis: 1
Route/Site: OT / -

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

Expired product administered

Symptomtext

expired dose administered to patient; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expired dose administered to patient) in a 66-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 065F21A and 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 08-Feb-2022, received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 08-Feb-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced EXPIRED PRODUCT ADMINISTERED (expired dose administered to patient). On 08-Feb-2022, EXPIRED PRODUCT ADMINISTERED (expired dose administered to patient) had resolved. 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 the vaccine was removed from the freezer and placed in the refrigerator and given the 30 day expiration date of 02-Feb-2022. It was kept at the designated temperature in the refrigerator until it was administered on 08-Feb-2022. The lot number was reported as 065F21A with expiration date of 04-Feb-2022. It was reported symptoms were unknown at the time of reporting. No treatment medications were provided. Most recent FOLLOW-UP information incorporated above includes: On 08-Feb-2022: Follow-up received. Added patient demographics(initials, date of birth, age and gender) and first dose details.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2104322

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: F
Eingang: 11.02.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: UNK
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F; Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion/10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F) had resolved. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Dose was administered in deltoid muscle. No concomitant medications were reported. No treatment information was provided.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2104318

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: -
Geschlecht: M
Eingang: 11.02.2022
Impfdatum: -
Beginn: -
Tage bis Beginn: -
Dosis: 3
Route/Site: OT / -

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

Product storage error Product temperature excursion issue

Symptomtext

Vaccine administered after temperature excursion; Vaccine administered after temperature excursion; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Vaccine administered after temperature excursion) and PRODUCT STORAGE ERROR (Vaccine administered after temperature excursion) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. It was reported that total 19 patients received expired vaccine out of which 3 were males and 16 were females. It was reported that 10 vials of 15 doses each were stored in a freezer which temperature range was at all times from 24.3?F to 24.7?F. HCP mentioned that they always had the freezer between this range. Two vials were used to administered HCP's office employees. All doses were injected intramuscularly in deltoid muscle. Vaccine administration dates were reported as 23-Nov-2021 and 27-Nov-2021. No concomitant medication reported No treatment medication reported

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product storage error
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2095665

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: 69,0
Geschlecht: M
Eingang: 08.02.2022
Impfdatum: -
Beginn: 16.01.2022
Tage bis Beginn: -
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

Event occurred after 3rd vaccine; breakthrough case.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: 1/16/2022 COVID-19 positive.
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2075534

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: 55,0
Geschlecht: M
Eingang: 31.01.2022
Impfdatum: 30.11.2021
Beginn: 30.11.2021
Tage bis Beginn: 0,0
Dosis: 2
Route/Site: IM / RA

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

Inappropriate schedule of product administration

Symptomtext

Dose given too soon. Dose given at 21 days, not 28 days.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2062161

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: MI
Alter: 83,0
Geschlecht: M
Eingang: 25.01.2022
Impfdatum: 16.11.2021
Beginn: 23.01.2022
Tage bis Beginn: 68,0
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

COVID vaccine breakthrough case

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: COVID positive test 1/23/2022
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2054178

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: 16,0
Geschlecht: M
Eingang: 21.01.2022
Impfdatum: 21.12.2021
Beginn: 21.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / -

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

Product administered to patient of inappropriate age

Symptomtext

16 year old client received Moderna COVID 19 vaccine as a booster by parent request.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: n/a
Aktuelle Erkrankungen: N/A
Vorgeschichte: N/a
Andere Medikamente: N/a
Allergien: N/A
Vorherige Impfungen: -

VAERS 2045533

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: CA
Alter: 50,0
Geschlecht: F
Eingang: 19.01.2022
Impfdatum: 05.01.2022
Beginn: 05.01.2022
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Inappropriate schedule of product administration

Symptomtext

Error: Booster given too early.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2043020

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: -
Alter: 58,0
Geschlecht: F
Eingang: 18.01.2022
Impfdatum: 24.02.2021
Beginn: 09.08.2021
Tage bis Beginn: 166,0
Dosis: UNK
Route/Site: IM / RA

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

COVID-19 SARS-CoV-2 test positive

Symptomtext

Patient fully vaccinated for COVID-19 tested positive for COVID-19.

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 2035397

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: OK
Alter: 59,0
Geschlecht: F
Eingang: 14.01.2022
Impfdatum: 17.11.2021
Beginn: 11.01.2022
Tage bis Beginn: 55,0
Dosis: 3
Route/Site: IM / LA

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

COVID-19 Rhinorrhoea SARS-CoV-2 RNA SARS-CoV-2 test positive

Symptomtext

RN

Weitere VAERSDATA-Felder

Praegender Schweregrund: COVID-19
Hospital-Tage: -
Labordaten: POSITIVE SARS-COV-2 RNA
Aktuelle Erkrankungen: LACERATION OF RIGHT INDEX FINGER
Vorgeschichte: ALLERGIC RHINITIS, OBESITY
Andere Medikamente: CETIRIZINE
Allergien: NKA
Vorherige Impfungen: -

VAERS 1999394

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: TX
Alter: 80,0
Geschlecht: M
Eingang: 03.01.2022
Impfdatum: 29.10.2021
Beginn: 10.11.2021
Tage bis Beginn: 12,0
Dosis: UNK
Route/Site: SYR / RA

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

Atrial fibrillation Cardiac stress test normal Echocardiogram normal

Symptomtext

Went into Atrial Fibrillation Nov. 10, 2021 at around 5:30 am-two weeks after Booster. Taken to Hospital by EMS and symptoms lasted 24 hours. Out of A Fib at 6:05 am on 11/11/2021. No recurrence as of 1/3/2022.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Atrial fibrillation
Hospital-Tage: -
Labordaten: Echocardiogram, Nuclear stress test and results were fine.
Aktuelle Erkrankungen: none
Vorgeschichte: High blood pressure
Andere Medikamente: Omeprazole, Combigan, Crestor, Amlodipine, Bausch +lomb preservation AREDS, Folic acid , Omega-3, Vitamin D, Vitron C(iron),Baby aspirin
Allergien: none
Vorherige Impfungen: -

VAERS 1998475

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: DE
Alter: 67,0
Geschlecht: F
Eingang: 03.01.2022
Impfdatum: 06.12.2021
Beginn: 06.12.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: OT / -

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

Expired product administered Product storage error

Symptomtext

administered 2 doses from vials that were stored for more than 30 days at the fridge; administered 2 doses from vials that were stored for more than 30 days at the fridge; This spontaneous case was reported by a physician and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administered 2 doses from vials that were stored for more than 30 days at the fridge) and PRODUCT STORAGE ERROR (administered 2 doses from vials that were stored for more than 30 days at the fridge) in a 67-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. Concurrent medical conditions included Penicillin allergy and Drug allergy (Norvasc). On 06-Dec-2021 at 2:30 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 ml. On 06-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (administered 2 doses from vials that were stored for more than 30 days at the fridge) and PRODUCT STORAGE ERROR (administered 2 doses from vials that were stored for more than 30 days at the fridge). On 06-Dec-2021, EXPIRED PRODUCT ADMINISTERED (administered 2 doses from vials that were stored for more than 30 days at the fridge) and PRODUCT STORAGE ERROR (administered 2 doses from vials that were stored for more than 30 days at the fridge) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment details were provided. Dose was stored in the fridge on 3 Nov 2021. Patient had no adverse event. This case was linked to MOD-2021-406580 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: Drug allergy (Norvasc); Penicillin allergy
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1992978

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: 35,0
Geschlecht: F
Eingang: 30.12.2021
Impfdatum: 03.11.2021
Beginn: 08.11.2021
Tage bis Beginn: 5,0
Dosis: 3
Route/Site: - / LA

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

Breast discharge Magnetic resonance imaging breast Mammogram Ultrasound breast

Symptomtext

Brown discharge from left nipple noticed approximately 5 days after vaccine. This occured on the same side the vaccine was administered. A mammogram and ultrasound could not identify the cause of the discharge. I am currently awaiting the results of a breast MRI.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Breast discharge
Hospital-Tage: -
Labordaten: Breast mammogram 11/10/2021 Breast ultrasound 11/10/2021 Breast MRI 12/22/2021
Aktuelle Erkrankungen: N/A
Vorgeschichte: High blood pressure Overweight
Andere Medikamente: Lisinopril Hydrochlorothiazide
Allergien: Codine
Vorherige Impfungen: -

VAERS 1988799

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: CT
Alter: 60,0
Geschlecht: M
Eingang: 29.12.2021
Impfdatum: 30.11.2021
Beginn: 04.12.2021
Tage bis Beginn: 4,0
Dosis: 3
Route/Site: IM / LA

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

Muscular weakness Neuropathy peripheral Ophthalmological examination Uveitis

Symptomtext

Peripheral neuropathies: right arm radial nerve, right leg femoral nerve followed by muscle weakness (finger extensors, hip flexor) . Uveitis. Resolving after getting prescription prednisolone eye drops.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Muscular weakness
Hospital-Tage: -
Labordaten: Eye exam December 24th
Aktuelle Erkrankungen: -
Vorgeschichte: Auto immune disorders (vitiligo, hereditary neuralgic amyotrophy)
Andere Medikamente: Diazepam, vitamin D
Allergien: Dust, dust mites, cats
Vorherige Impfungen: -

VAERS 1984626

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: NC
Alter: 73,0
Geschlecht: M
Eingang: 28.12.2021
Impfdatum: 08.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 1,0
Dosis: 3
Route/Site: IM / LA

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

Vertigo positional

Symptomtext

Vertigo when getting up from lying down position, rolling over in bed and getting up after sitting down.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Vertigo positional
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: n/a
Vorgeschichte: prostate cancer remission
Andere Medikamente: Probiotic, digestive enzymes
Allergien: n/a
Vorherige Impfungen: -

VAERS 1981712

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: OH
Alter: 34,0
Geschlecht: F
Eingang: 27.12.2021
Impfdatum: 12.11.2021
Beginn: 21.12.2021
Tage bis Beginn: 39,0
Dosis: 3
Route/Site: IM / LA

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

Abdominal distension Amenorrhoea Anaemia Blood test normal Breast tenderness Full blood count abnormal Muscle spasms Pregnancy test urine negative

Symptomtext

Missed next menses. was to have have period in December. Had symptoms but no period. Symptoms of period/pregnancy - bloating, cramping and breast tenderness.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Abdominal distension
Hospital-Tage: -
Labordaten: 3 at home urine HCG all negative Blood work done 12/27/21 NEGATIVE results. CBC also done to check (CBC) slightly anemic at time of draw.
Aktuelle Erkrankungen: NONE
Vorgeschichte: NONE
Andere Medikamente: NONE
Allergien: NONE
Vorherige Impfungen: -

VAERS 1971667

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: 15,0
Geschlecht: F
Eingang: 22.12.2021
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: unbekannt Erholt: ja

Interchange of vaccine products Product administered to patient of inappropriate age

Symptomtext

Pharmacy held an immunization clinic for employees of a large local business at their office location. The patient, a 15-year-old, attended with her parents. We were offering COVID-19 boosters to employees and had both Pfizer and Moderna options for them. We were not expecting any pediatric patients to attend this event. The patient's DOB was overlooked, and she was given 0.25ml of the Moderna COVID-19 vaccine. She had previously been vaccinated with Pfizer COVID-19 vaccine; her last dose had been June 5, 2021.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Interchange of vaccine products
Hospital-Tage: -
Labordaten: none
Aktuelle Erkrankungen: none
Vorgeschichte: none
Andere Medikamente: none
Allergien: none
Vorherige Impfungen: -

VAERS 1971521

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: VA
Alter: 47,0
Geschlecht: F
Eingang: 22.12.2021
Impfdatum: 07.12.2021
Beginn: 09.12.2021
Tage bis Beginn: 2,0
Dosis: 3
Route/Site: IM / LA

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

Herpes zoster

Symptomtext

Pt developed zoster outbreak in T11 dermatome on the right, symptoms began within 48 h of vaccine dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Herpes zoster
Hospital-Tage: -
Labordaten: Seen at urgent care earlier this month; I do not yet have these records. Seen by me today.
Aktuelle Erkrankungen: none
Vorgeschichte: intermittent asthma (not on inhaled or oral steroids), obesity, vit D deficiency
Andere Medikamente: albuterol, diclofenac, Claritin, Alka-Seltzer chews, Aleve, Ibuprofen, RealTime Cream, Vit D/B Super Complex
Allergien: aspirin, gabapentin, erythromycin, PCN, olsetamivir
Vorherige Impfungen: -

VAERS 1971321

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: GA
Alter: 16,0
Geschlecht: M
Eingang: 22.12.2021
Impfdatum: 22.12.2021
Beginn: 22.12.2021
Tage bis Beginn: 0,0
Dosis: 1
Route/Site: IM / RA

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

Product administered to patient of inappropriate age

Symptomtext

PATIENT IS 16, WHICH IS UNDER THE AGE OF 18 FOR WHICH THE VACCINE SHOULD BE ADMINISTERED TO.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1961166

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: WA
Alter: 73,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Expired product administered

Symptomtext

Received expired vaccine administered >12(US)/ hours post puncture; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered >12(US)/ hours post puncture) in a 73-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Dec-2021 at 8:00 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered >12(US)/ hours post puncture). On 14-Dec-2021, EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered >12(US)/ hours post puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication were reported. No treatment information was provided by the reporter. Patient received expired Moderna COVID-19 vaccine from a vial that was punctured for more than 12 hours (first punctured on 13-DEC-2021 at 2:58PM , and administered on 14-DEC-2021 at 8AM). The vial was initially stored in the refrigerator on 29-Oct-2021.The vial did not undergo any temperature excursions. The vial was stored post puncture in room temperature. Total amount of time the vial was exposed to room temperature range (8? to 25?C 46? to 77?F) was 17.5 hours. This case was linked to MOD-2021-414574, MOD-2021-414607, MOD-2021-414618, MOD-2021-141623 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1961163

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: WA
Alter: 68,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Expired product administered

Symptomtext

Received expired vaccine administered >12(US)/ hours post puncture; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered >12(US)/ hours post puncture) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Dec-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered >12(US)/ hours post puncture). On 14-Dec-2021, EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered >12(US)/ hours post puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. Treatment medications were not reported. The vial was initially stored in the refrigerator on 29-Oct-2021 and was first punctured on 13-Dec-2021. Therefore total amount of time the vial was exposed to room temperature was 17.5 hours. This case was linked to MOD-2021-414574 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1961162

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: WA
Alter: 72,0
Geschlecht: F
Eingang: 18.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Expired product administered

Symptomtext

Received expired vaccine administered, vial was kept greater than 12/ hours post puncture; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered, vial was kept greater than 12/ hours post puncture) in a 72-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Dec-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered, vial was kept greater than 12/ hours post puncture). On 14-Dec-2021, EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered, vial was kept greater than 12/ hours post puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Nurse called to report that patient received expired Moderna COVID-19 vaccine from a vial that was punctured more than 12 hours (first punctured on 13-Dec-2021 at 2:58PM , and administered on 14-Dec-2021 at 8AM). The vial was initially stored in the refrigerator on 29-Oct-2021.The vial did not undergo any temperature excursions. Total amount of time the vial was exposed to room temperature range (8 degree Celsius to 25?degree Celsius = 46 degree Fahrenheit to 77 degree Fahrenheit) was 17.5 hours 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 1961159

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: WA
Alter: 65,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Expired product administered

Symptomtext

Received expired vaccine administered >12/ hours post puncture; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered >12/ hours post puncture) in a 65-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Dec-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered >12/ hours post puncture). On 14-Dec-2021, EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered >12/ hours post puncture) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication reported. No treatment information was provided. This case was linked to MOD-2021-414692 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1961157

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: WA
Alter: 71,0
Geschlecht: M
Eingang: 18.12.2021
Impfdatum: 14.12.2021
Beginn: 14.12.2021
Tage bis Beginn: 0,0
Dosis: UNK
Route/Site: OT / -

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

Expired product administered

Symptomtext

Received expired vaccine administered >12/ hours post puncture; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered >12/ hours post puncture) in a 71-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 033F21A) for COVID-19 vaccination. No Medical History information was reported. On 14-Dec-2021 at 8:00 AM, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Dec-2021, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered >12/ hours post puncture). On 14-Dec-2021, EXPIRED PRODUCT ADMINISTERED (Received expired vaccine administered >12/ hours post puncture) had resolved. 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. This case was linked to MOD-2021-414692 (Patient Link).

Weitere VAERSDATA-Felder

Praegender Schweregrund: Expired product administered
Hospital-Tage: -
Labordaten: -
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -

VAERS 1959189

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

gering

Staat: MA
Alter: 53,0
Geschlecht: M
Eingang: 17.12.2021
Impfdatum: 13.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / LA

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

Underdose

Symptomtext

Error: Wrong Dose of Vaccine - Too Low-

Weitere VAERSDATA-Felder

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

VAERS 1955853

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

gering

Staat: NY
Alter: 41,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 03.12.2021
Beginn: 13.12.2021
Tage bis Beginn: 10,0
Dosis: 3
Route/Site: SYR / LA

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

Herpes zoster

Symptomtext

Shingles rash on mid back, left side of body, treated with valacylovir

Weitere VAERSDATA-Felder

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

VAERS 1954777

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: NJ
Alter: 65,0
Geschlecht: F
Eingang: 16.12.2021
Impfdatum: 24.02.2021
Beginn: 27.02.2021
Tage bis Beginn: 3,0
Dosis: UNK
Route/Site: - / LA

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

Biopsy Blood test Lip discolouration Oral mucosal blistering

Symptomtext

BLISTERS IN MOUTH AFTER 2ND MODERNA COVID 19 VACCINE STARTED AFTER A WEEK FROM GETTING THE VACCINE. LASTED FOR ABOUT 8 MONTHS AND STILL GETTING OCCASSIONALY. ALSO HAD DISCOLORATION ON MY LIPS WHICH KEPT GROWING.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Biopsy
Hospital-Tage: -
Labordaten: BIOPSY BY ORAL SURGEN FOR AUTO IMMUNE PROCESS (COULD NOT DO BIOPSY FROM BLISTERS AS AT THE TIME OF MY VISIT IT WAS NOT IN PRESENT SO BIOPSY WAS DONE FROM SIDE OF MY CHEEK. HAD ENT GAVE ME STEROID MOUTH WASH WHICH DID NOT HELP. SAW DERMATOLOGIST HAD BLOOD WORK DONE FOR FOR DESMOGLEIN 1 AND 3, VEMIPUNCTURE CAME WITH DEMOGLEIN 1 ANTIBODY POSITIVE TO 22.3 (ABNORMAL). HAD RHEUMOTOLOGIST APPT AND RAN BLOOD WORK AND FOUND ABNORMAL PROTEIN IN MY BONE MARROW AND WAS REFERRED TO HEMATOLOGIST AND DIAGNOSED WITH MGUS.
Aktuelle Erkrankungen: NONE.
Vorgeschichte: OSTEOPOROSIS.
Andere Medikamente: ALGAE CAL BOOST & ALGAE CAL STANTIUM FOR OSTIOPOROSIS.
Allergien: NONE.
Vorherige Impfungen: -

VAERS 1948000

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033f21a

gering

Staat: OR
Alter: 21,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 09.11.2021
Beginn: 09.11.2021
Tage bis Beginn: 0,0
Dosis: 3
Route/Site: IM / RA

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

Inappropriate schedule of product administration

Symptomtext

Patient presented to clinic for a booster dose of Moderna. Patient had received her 1st dose on 5/20/21 and 2nd dose on 6/16/21. She received her booster dose, (Moderna, 0.25 ml dose) on 11/09/21 , approximately 37 days before she should of received her booster dose.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Inappropriate schedule of product administration
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: unknown
Vorgeschichte: unknown
Andere Medikamente: unknown
Allergien: NKDA
Vorherige Impfungen: -

VAERS 1947587

MODERNA · COVID19 (COVID19 (MODERNA)) · Charge 033F21A

gering

Staat: OH
Alter: 12,0
Geschlecht: M
Eingang: 14.12.2021
Impfdatum: 12.11.2021
Beginn: 13.11.2021
Tage bis Beginn: 1,0
Dosis: 1
Route/Site: IM / LA

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

Product administered to patient of inappropriate age Wrong product administered

Symptomtext

Patient is 12 years old and mistakenly received Moderna Covid-19 vaccine instead of Pfizer. No known harm to the patient.

Weitere VAERSDATA-Felder

Praegender Schweregrund: Product administered to patient of inappropriate age
Hospital-Tage: -
Labordaten: None
Aktuelle Erkrankungen: -
Vorgeschichte: -
Andere Medikamente: -
Allergien: -
Vorherige Impfungen: -