- Staat
- FL
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 22.05.2023
- Impfdatum
- 11.02.2022
- Beginn
- 20.04.2023
- Tage bis Beginn
- 433,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
COVID-19
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 4/15/2023 - 4/20/2023 (5 days) Presentation to the ED: acute respiratory failure COVID + date: 4/20/2023 Treatment: Remdesivir Discharge to: HOME. 006B21A 3/17/2021 037B21A 4/17/2021 046L21A 2/11/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- MI, T2DM, HLD, HTN
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 28.11.2022
- Impfdatum
- 09.05.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 23,0
- Dosis
- 5
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram cerebral
Arteriogram carotid
Blood test
Cerebrovascular accident
Computerised tomogram
Condition aggravated
Magnetic resonance imaging
Platelet count decreased
Symptomtext
I had my vaccination on 05/09/2022. On 06/01/2022 I had a stroke. I was taken to the emergency room. I was given a blood panel in which the platelets were shown to be decreasing. I had had the second stroke in a year. I was in the hospital for 10 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 10,0
- Labordaten
- 06/01/2022 blood panel; MRI; CAT scan; angiogram of brain and neck; shown to have decreasing platelets and stroke.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- WELLBUTRIN; PROZAC; aspirin
- Allergien
- CELEBREX; penicillin
- Vorherige Impfungen
- COVID-19 11/20/21 stroke
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 21.09.2022
- Impfdatum
- 05.04.2022
- Beginn
- 27.04.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Death 22 days after vaccine dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- zolpidem, montelukast, budesonide-fomoterol
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 12.09.2022
- Impfdatum
- 15.03.2022
- Beginn
- 28.08.2022
- Tage bis Beginn
- 166,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute kidney injury
Angiogram cerebral normal
Anticoagulant therapy
Atrioventricular block complete
Atrioventricular block second degree
Bladder catheterisation
Blood culture positive
COVID-19
Cardio-respiratory arrest
Chills
Computerised tomogram abdomen abnormal
Computerised tomogram head normal
Death
Duodenal ulcer
Dysarthria
Echocardiogram
Electrocardiogram T wave abnormal
Electrocardiogram T wave inversion
Symptomtext
Discharge Provider: Primary Care Physician at Discharge: MD Admission Date: 8/28/2022 PRESENTING PROBLEM: Shock (HCC) [R57.9] MSSA bacteremia [R78.81, B95.61] HOSPITAL COURSE: 62 y.o.male with past medical history of severe aortic stenosis, provoked DVT (2018) not on current anticoagulation, right retinal branch occlusion (03/2022), carotid dissection, and alcohol use disorder who presented after a ground level fall at home. EMS was called to the home and noticed possible right sided facial droop and slurred speech without extremity deficits. On arrival to the emergency department, the patient was hypotensive, tachycardic, and febrile. Code stroke was called and CT head, CT perfusion, and CT angio were negative for acute stroke. An additional finding on imaging was mild T1-T3 superior endplate compression fractures. Lab work was notable for hyponatremia (126), AKI, lactic acidosis, leukocytosis, elevated troponin, and Covid +. Sepsis protocol was initiated with the patient receiving 4L IVF, but ultimately necessitating pressor support. EKG also revealed new T wave inversions and T wave depressions in V1-V6. Heparin gtt was initiated due to concern for NSTEMI. The patient was transferred to MICU for further care. Further workup included blood cultures (positive for MSSA), CT abdomen/pelvis (scattered pulmonary nodules; lesion in segment 6 of the liver; marked enlargement of the right ureter and large right ureterocele), RUQ US (lesion in segment 6 revealed to be hemangioma), stool studies (negative), TTE (without wall motion abnormalities, LVEF preserved), and MRI brain (several scattered foci of restricted diffusion involving bilateral occipital lobes, inferior left cerebellum, and superior right cerebellar hemisphere). The constellation of symptoms and findings is suspicious for infectious endocarditis. Cardiology consulted. Infectious disease consulted. Patient was started on ancef for infective endocarditis. Hospital course further complicated by GIB with hemoglobin drop. GI consulted - patient underwent EGD that showed duodenal ulceration with visible vessel spontaneously oozing status post epinephrine injection into clipped with hemostasis achieved. The next day the patient started having bloody bowel movements and blood clots. Another EGD did not show any acute findings. Additionally, patient underwent Flex sigmoidoscopy which revealed No heme in rectal vault and a Large prolapsing hemorrhoids. Colorectal surgery consulted and managed conservatively. Additionally, the patient started having hematuria therefore a Foley catheter was placed and intermittent irrigation was applied with flushes. Patient developed worsening vitals and chills, CTAP and HIDA revealed concerns for cholecystitis. Antibitoics changes to cefepime and flagyl and IR and surgery consulted. 9/7, patient developed type 2 heart block with further progression to episodes of complete heart block. Patient underwent TEE which revealed concerns for aotic valve abscess. Ultimately on 9/9 patient developed v fib arrest, code blue was called and were unable to achieve ROSC despite multiple rounds of CPR and epi. Patient ultimately expired 9/9/2022 @ 13:05pm. Wife and daughter at bedside during code.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardio-respiratory arrest
- Hospital-Tage
- 12,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic deep vein thrombosis (DVT) of left peroneal vein (HCC) Presbyopia Vitreous floater, left Combined forms of age-related cataract, bilateral Bilateral lower extremity edema Tobacco user Heavy alcohol consumption Abnormal EKG Systolic murmur Preop cardiovascular exam Retinal artery branch occlusion of right eye Internal carotid artery dissection (HCC) Elevated BP without diagnosis of hypertension Shock (HCC) MSSA Aortic and mitral valve endocarditis complicated by Aortic root abscess COVID-19 Mitral valve vegetation Nonrheumatic aortic valve stenosis Found to have large prolapsing hemorrhoids s/p flexible sigmoidoscopy on 9/4/2022 for acute GI bleed
- Andere Medikamente
- Blood Pressure Monitoring (BLOOD PRESSURE CUFF) MISC ceFAZolin (ANCEF) 1 g injection CBD Gummies
- Allergien
- Pollen
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 09.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Exposure during pregnancy
Foetal death
Foetal hypokinesia
Platelet count decreased
Vaginal haemorrhage
Symptomtext
Patient received her Booster at 14w1d gestation and began bleeding the following morning. She had intermittent bleeding until 19w6d when she was found to have intrauterine fetal demise. She was examined that day due to decreased fetal movement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Foetal death
- Hospital-Tage
- 1,0
- Labordaten
- Platelet counts 04/25/22 09:45K/uL 148 04/17/22 13:10K/uL 87 04/12/22 06:10 K/uL 86 04/05/22 09:24 K/uL 105 3/14/22 79
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Gestational thrombocytopenia Polycystic Kidney disease Bicornate uterus Hypothyroidism
- Andere Medikamente
- Prenatal Vitamin Progesterone
- Allergien
- NOne
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 18.04.2022
- Impfdatum
- 22.03.2022
- Beginn
- 27.03.2022
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Death
Feeling hot
Resuscitation
Unresponsive to stimuli
Symptomtext
Resident reported he was feeling Hot and requested for Air to be turn on and also requested for a Cup of Ice. All his request was Provided. At 8:52am Resident was checked and told writer he feels better and requested for Ice this time which was provided. At about 10:15am writer went to administer Resident meds and found resident on unresponsive. Pt is full code so CPR initiated,911 called and V/S during CPR was B/P, 218/161,175,BS 159.911 arrived at 10:25 and took over CPR.RP made aware of changes. Resident pronounced Deceased by 911 at 10:50pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Gout, HTN, Hyperlipidemia, spinal stenosis, deep vein thrombosis
- Andere Medikamente
- Allopurinol, amloddipine, Aspirin, Lipitor, Lisinopril, Predni
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Breath sounds abnormal
Condition aggravated
Death
Dyspnoea
Feeding disorder
Fluid intake reduced
Gait disturbance
Heart rate increased
Hypopnoea
Livedo reticularis
Oxygen saturation decreased
SARS-CoV-2 test negative
Tachypnoea
Unresponsive to stimuli
Symptomtext
Resident began to have increased weakness on 2/26/22 at approximately 6pm. Resident normally ambulates independently, but resident required assistance of staff to walk to and from the dining room for supper. At approximately 6:05am on 2/27/22, resident had an elevated pulse rate of 125, rapid and shallow respirations of 40, labored breathing, O2 sat dropping to 88%, blood pressure 147/89, temperature 98.2 degrees, diminished lung sounds, and unresponsiveness. Oxygen was applied at 2L/NC. Resident was tested for Covid at facility, and results were negative at 8:40am. Resident was unable to eat or drink, and nursing staff administered morphine sulfate as needed per orders. At 6:18pm, temperature 98.4 degrees, and nurse was unable to obtain blood pressure, pulse, or oxygen saturation with facility equipment, and resident continued to remain unresponsive. At 10:55pm, resident's oxygen saturation was 67% on 1.5L/NC, temperature 99.3 degrees, respirations 14, and resident was gasping with shallow breaths. Mottling noted to extremities. Resident passed away at 11:25pm on 2/27/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- Covid antigen test on 2/27/22at 8:25am - results negative at 8:40am.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Senile degeneration of brain, dementia, GERD, anxiety, hypokalemia, depression, hypertension, weakness, hypercholesterolemia, Type 2 diabetes without complications
- Andere Medikamente
- aspirin, donepezil, hydrochlorothiazide, lorazepam, losartan, memantine, potassium chloride, sertraline, simvastatin
- Allergien
- Niaspan Extended-Release, Nickel, Penicillin, Victoza, Pineapple, Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Symptomtext
Pt had does Thursday morning, went to bed feeling fine with no complaints, found expired Friday am
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- fluctuating BP
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- dehydrated from nausea/vomiting after Pftizer #2 Covid and fell
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 22.05.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose
Fatigue
Myalgia
Syncope
Vitamin B12
Vitamin D
Symptomtext
fainting; fatigue; muscle aches; This spontaneous case was reported by a patient and describes the occurrence of SYNCOPE (fainting) in a 61-year-old female patient who received mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (batch nos. 046L21A and 025L21B) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. The patient's past medical history included Thyroid disorder and Hashimoto's disease. On an unknown date, the patient received second dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced SYNCOPE (fainting) (seriousness criterion medically significant), FATIGUE (fatigue) and MYALGIA (muscle aches). At the time of the report, SYNCOPE (fainting), FATIGUE (fatigue) and MYALGIA (muscle aches) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Blood glucose: fluctuating for her abnormally. On an unknown date, Vitamin B12: vitamin B12 deficiency. On an unknown date, Vitamin D: vitamin D deficiency. For mRNA-1273 BIVALENT .222 (MODERNA COVID-19 VACCINE, BIVALENT (ORIGINAL AND OMICRON BA.4/BA.5)) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment medications were reported. Company comment This spontaneous case concerns a 61-year-old female patient with medical history of Thyroid issues all her life and Hashimoto diagnosis, who experienced the serious (medically significant), unexpected event of Syncope. The patient received the first and second doses of mRNA-1273.222 (BA.4/BA.5). The event onset date and vaccination date were not provided, thus, exact latency between vaccination and onset of the events could not be assessed. Other non-serious events include fatigue and muscle aches that could be associated with D3 deficiency, B12 deficiency and the medical history of Hashimoto. It was reported that she was seeking treatment through her HCP. No further clinical information was provided for medical review. The benefit-risk relationship of mRNA-1273.222 (BA.4/BA.5) is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- Test Name: Blood sugar level; Result Unstructured Data: fluctuating for her abnormally; Test Name: vitamin B12; Result Unstructured Data: vitamin B12 deficiency; Test Name: vitamin D; Result Unstructured Data: vitamin D deficiency
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Medical History/Concurrent Conditions: Hashimoto's disease; Thyroid disorder
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 08.11.2022
- Impfdatum
- 18.02.2022
- Beginn
- 21.09.2022
- Tage bis Beginn
- 215,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Antiplatelet therapy
Atrial fibrillation
Blood creatinine normal
Cardiac failure acute
Cardiac failure congestive
Cardiac telemetry
Chest X-ray abnormal
Chest discomfort
Condition aggravated
Coronary artery disease
Dyspnoea
Dyspnoea at rest
Echocardiogram
Ejection fraction decreased
Electrocardiogram abnormal
Gastrooesophageal reflux disease
Haemoglobin decreased
Left ventricular failure
Symptomtext
Document Type: History and Physical Document Subject: History & Physical Note Performed By: MD on September 21, 2022 16:31 EDT Verified By: MD on September 21, 2022 16:31 EDT Encounter Info: Hospital, Inpatient, 09/21/22 - 09/30/22 * Final Report * Document Has Been Revised Chief Complaint Shortness of breath History of Present Illness/Subjective Patient is a 72 year old woman who presents to Hospital w/ SOB. The patient reports that for the last few days she has had worsening shortness of breath. She also endorses some chest tightness. She cannot lie flat at all as this make sure SOB much worse. Upon arrival to the hospital she was satting normally on RA and normotensive but was tachypneic. EKG showed sinus tachycardia. CxR showed bilateral pleural effusions and pulmonary edema. Trop was mildly elevated. Here trop is 19 and EKG is unchanged. Hgb was 10. Cr was normal. Her case was discussed w/ her Cardiologist Dr. who recommended admission to hospital for further management. Upon arrival here the patient is on RA but endorses SOB particularly when not sitting upright. She has some chest tightness but no frank chest pain. No new complaints and the remainder of her vitals are stable. Review of Systems With the exception of that noted in the HPI all systems were reviewed and were negative. Physical Exam/Objective Vital Signs (most recent and range for last 24 hours) Temp (CEL) 36.5 (36.5-36.5) Temp (FAHR) 97.7 (97.7-97.7), BP 101/66 (101-101)/(66-66), HR 93 (93-93), RR 22 (22-22), O2Sat 91 (91-91) Patient Height Current Height: 165.1 cm Constitutional: No acute distress, well-nourished Eyes: no scleral icterus ENMT: Moist oral mucosa Respiratory: Breathing comfortably on room air Cardiovascular: Regular rate and rhythm Gastrointestinal: non-distended Musculoskeletal: intact ROM Integumentary: no rashes Neurologic: no focal deficits Psychiatric: Cooperative, appropriate mood and affect Assessment/Plan Patient is a 72 year old woman admitted w/ pulmonary edema due to a CHF exacerbation. 2. Elevated troponin R77.8 -Serial troponin -EKG w/out acute ischemic changes -Nitro paste to ensure patient is CP free 3. GERD (gastroesophageal reflux disease) K21.9 -Continue PPI 4. PAF (paroxysmal atrial fibrillation) I48.0 -Continue amiodarone and apixaban 5. CAD in native artery I25.10 -Continue DAPT and statin 6. Acute on chronic systolic CHF -Lasix 40mg IV q12H -Low sodium diet, 1500cc/day fluid restriction -TTE -Dr. consulted -Strict I/Os, daily weights -Telemetry -Nitro paste for preload reduction -Most recent EF of 20% -Life vest can be removed as long as patient is on telemetry Code Status Resuscitation Status - Ordered -- 09/21/22 15:54:00 EDT, Full Code Chronic Problem List Arthritis Family history of colon cancer GERD (gastroesophageal reflux disease) Hemorrhoids IBS (irritable bowel syndrome) Procedure/Surgical History ?Colonoscopy (03/26/2019) ?knee replacement (10/2014) ?Colonoscopy (03/26/2014) ?Esophagogastroduodenoscopy and biopsy (02/02/2011) ?heart stent (1997) ?Appendectomy ?Cholecystectomy ?Tonsillectomy Medications Home Medications (21) Active Allegra Allergy 1 Tablet, Orally, Daily amiodarone 200 mg oral tablet 200 mg = 1 Tablet, Orally, Daily atorvastatin 40 mg oral tablet 40 mg = 1 Tablet, Orally, At Bedtime azelastine nasal 0.1% spray 1 Spray, intraNASAL, Daily carvedilol 6.25 mg oral tablet 6.25 mg = 1 Tablet, Orally, BID cholecalciferol (vitamin D3) 25 mCg (1,000 intl units) oral tablet 25 mCg = 1 Tablet, Orally, Daily clopidogrel 75 mg oral tablet 75 mg = 1 Tablet, Orally, Daily Co-Q10 100 mg oral capsule 100 mg = 1 Capsule, Orally, Daily Eliquis 5 mg oral tablet 5 mg = 1 Tablet, Orally, BID ezetimibe 10 mg oral tablet 10 mg = 1 Tablet, Orally, Daily furosemide 40 mg oral tablet 40 mg = 1 Tablet, Orally, Daily hydrOXYzine hydrochloride 25 mg oral tablet 25 mg = 1 Tablet, PRN, Orally, Q6H losartan 25 mg oral tablet 25 mg = 1 Tablet, Orally, Daily metFORMIN 500 mg oral tablet 4 tablets, Orally, Daily montelukast 10 mg oral tablet 10 mg = 1 Tablet, Orally, Every PM Nature's Bounty Hair Skin & Nails oral tablet, chewable 1 Tablet, Orally, Daily Neuriva Brain performance Plus 1 Capsule, Orally, Daily nitroGLYCerin 0.4 mg sublingual tablet 0.4 mg = 1 Tablet, Sublingually, Q5min Ocuvite 1 Tablet, Orally, Daily traZODONE 100 mg oral tablet 100 mg = 1 Tablet, Orally, At Bedtime Vitamin B12 1000 mCg oral tablet 1,000 mCg = 1 Tablet, Orally, Daily Active Scheduled Inpatient Medications amiodarone, Tablet, 200 mg, Orally, Daily, Start: 09/22/22 09:00:00 apixaban, Tablet, 5 mg, Orally, BID, Start: 09/21/22 21:00:00 atorvastatin, Tablet, 40 mg, Orally, At Bedtime, Start: 09/21/22 21:00:00 carvedilol, Tablet, 6.25 mg, Orally, BID, Start: 09/21/22 21:00:00 cholecalciferol, Tablet, 25 mCg, Orally, Daily, Start: 09/22/22 09:00:00 clopidogrel, Tablet, 75 mg, Orally, Daily, Start: 09/22/22 09:00:00 cyanocobalamin, Tablet, 1,000 mCg, Orally, Daily, Start: 09/22/22 09:00:00 enoxaparin, Injection, 40 mg, Subcutaneous, Q24H, Start: 09/21/22 21:00:00 ezetimibe, Tablet, 10 mg, Orally, Daily, Start: 09/22/22 09:00:00 furosemide, Injection, 40 mg, IV Push, Q12, Start: 09/21/22 21:00:00 loratadine, Tablet, 10 mg, Orally, Daily, Start: 09/22/22 09:00:00 losartan, Tablet, 25 mg, Orally, Daily, Start: 09/22/22 09:00:00 montelukast (montelukast 10 mg oral tablet), Tablet, 10 mg, Orally, Every PM, Start: 09/21/22 18:00:00 traZODONE, Tablet, 100 mg, Orally, At Bedtime, Start: 09/21/22 21:00:00 One-Time Medications Given 09/20/22 00:00:00 TO 09/21/22 16:27:02 nitroGLYCerin (nitroGLYCerin 2% transdermal ointment), Ointment, 0.5 Inches, Topical, ONCE, (1 DOSE 09/21/22 16:19:00) PRN Medications (0600 - 0559) from 09/20 - 09/21 None Reported Allergies penicillins (Swelling Lip) lisinopril (Unknown) Tetanus Toxoid (Unknown) Social History Alcohol Current, 1-2 times per week Electronic Cigarette/Vaping E-Cigarette Use Never. Substance Abuse Denies Tobacco Tobacco Use: Never (less than 100 in lifetime). Family History Atrial septal defect..: Negative: Mother and Father. Breast cancer: Sister. Colon cancer..: Negative: Sister. Diabetes..: Mother and Father. Heart disease..: Father and Brother. Throat cancer..: Father. Lab Results All Labs Last 24 hours (No Micro or Pathology) Chemistry: Troponin-I High Sensitivity: 19 ng/L High (09/21/22 15:48:00) Diagnostics Radiology Results - Last 24 hours Across Visits No radiology results found in the last 24 hours. Signature Line Electronically Signed on 09/21/22 16:31 EDT ________________________________________________________ MD Electronically Signed on 09/21/22 17:11 EDT ________________________________________________________ MD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary oedema
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 05.08.2022
- Impfdatum
- 17.08.2021
- Beginn
- 02.08.2022
- Tage bis Beginn
- 350,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Influenza
Pyrexia
SARS-CoV-2 test positive
Seizure
Symptomtext
Pt admitted on 7/26 post seizure. Pt has a history of a right MCA stroke. Was found to have influenza A. Tested positive for COVID-19 on 8/2 after having fevers the day prior.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anaphylactic reaction
Blindness
Body temperature increased
Dizziness
Eye irritation
Eye pain
Eyelid skin dryness
Ophthalmological examination abnormal
Throat tightness
Vision blurred
Symptomtext
pt stated she started having like an anaphylaxis reaction about 15 minutes after getting the booster shot. Her throat was closing up and she was light headed. After about half hour she decided to drive home. Her vision was blurry and she had a tempurature of 102. She contacted her PCP and she was told to her eye doctor which she had seen recently. She saw her Eye physician and he compared the condition of her eyes from the last visit. She was told there was drastic change from the last visit to this visit. Her eyes were burning and were painful. There are dry patches on them. She had some vision loss. She was advised not to use her eye drops at the time due to the condition her eyes were in. She will try Sustain gel when her eyes are better to help them heal. She is using a mask at night which helps a little and also using a cool cloth. She will have to FU for further treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Anaphylactic reaction
- Hospital-Tage
- -
- Labordaten
- eye exam
- Aktuelle Erkrankungen
- Asthma since June 2021 and hopsitalized in April and June w/Pneumonia.
- Vorgeschichte
- Asthma, Bell's palsy, previous stroke, outdoor allergies, Bi-polar, eczema, major depressive disorder herniated wrist, displaced right knee cap, chronic sleep issues (nightmares) suicide overdose (full arrest), nerve tendon skin graphs (skin from ankle put on the wrist) ankle repair of ligaments that were torn, amputation of left index finger, 5 ectopic pregnancies (1 set of twins)
- Andere Medikamente
- Seroquel 300mg, omeprazole 40mg, viibryd tab 40mg, clonazepam, Benztropine .5 mg, prazosin 1mg, bupropion hydrochloride ext rel 300mg, propranolol 10mg x3 daily, vraylar 1.5 mg, ropinirole hydrochloride E tab .25 mg, famotidine 40mg, levoce
- Allergien
- triamcinolone Acetate, Geodon, silvadene, magnesium, Baclofen, latex, betadine gentamicin, leather, Pneumonia vaccine, tape, ziprasidone, bulizer machine, vucrisa, ketoconazole cream 2%, equate brand naproxen 220 mg,
- Vorherige Impfungen
- Pneumonia vaccine- she was already hospitalized w/ Pneumonia when she was given this vaccine and then had reaction to the vaccin
- Staat
- AL
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 01.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Syncope
Unresponsive to stimuli
Vomiting
Symptomtext
Systemic: Dizziness / Lightheadness-Mild, Systemic: Fainting / Unresponsive-Mild, Systemic: Vomiting-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Syncope
Unresponsive to stimuli
Symptomtext
Systemic: Fainting / Unresponsive-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 17.03.2022
- Beginn
- 17.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Cough
Interchange of vaccine products
Respiratory distress
Wheezing
Symptomtext
Janssen first dose and Moderna Booster Pt reported Respiratory distress including wheezing, coughing. Vitals: 156/82, 83, 26, 100% -- > 155/80, 67, 20, 100%. Pt given 25mg PO benadryl @09:21. Pt also took her own Norvasc 10mg. Pt stable and released from the vaccination site. Pt was able to stand and ambulate w/ no distress. Recommended f/u w/ PCP.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Respiratory distress
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: HTN, Migraine w/ Aura, PTSD, Asthma, Anxiety, OA Knee
- Andere Medikamente
- Medications: Fluticasone (FLONASE ALLERGY RELIEF) 50 mcg/actuation Nasl SpSn Indications: COUGH, UNSPECIFIED USE 2 SPRAYS IN EACH NOSTRIL DAILY FOR 1 WEEK, THEN MAY ADJUST TO 1 OR 2 SPRAYS IN EACH NOSTRIL DAILY Acetaminophen (PAIN RELIEF
- Allergien
- Allergies: Iodine and Iodide Containing Products (Anaphylaxis)
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 16.03.2022
- Impfdatum
- 16.03.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Syncope
Symptomtext
fainted and dizziness
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 10.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Flushing
Hyperhidrosis
Injection site erythema
Seizure like phenomena
Syncope
Tremor
Unresponsive to stimuli
Symptomtext
Site: Redness at Injection Site-Mild, Systemic: Dizziness / Lightheadness-Severe, Systemic: Fainting / Unresponsive-Severe, Systemic: see below-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Shakiness-Severe, Additional Details: Patient was shaking as if having a seizur no history, lasted roughly 10 seconds, snapped out of it, then just dizzy, sweaty, light headed. Said he has severe anxiety for which he is on disability for the last 10 years
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure like phenomena
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 06.03.2022
- Impfdatum
- 11.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest pain
Pulmonary thrombosis
Symptomtext
PATIENT WAS ADMITTED TO THE EMERGENCY ROOM DUE TO CHEST PAINS. UPON EXAMINATION, PATIENT HAD SEVERAL BLOOD CLOTS IN BOTH LUNGS. PATIENT WAS TREATED AND RELEASE AND TOLD TO REPORT ADVERSE REATION TO THE PHARMACY. THE PATIENT STATED THAT THE BLOOD CLOTS OCCURRED 8 DAYS AFTER RECEIVING MODERNA BOOSTER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- - HIGH BLOOD PRESSURE - BLOOD CLOTS
- Vorgeschichte
- - HIGH BLOOD PRESSURE - BLOOD CLOTS
- Andere Medikamente
- - ATORVASTATIN - LOSARTAN - ELIQUIS - AMLODIPINE - CERTIRIZINE
- Allergien
- NO ALLERGIES LISTED AT TIME OF VACCINE.
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 05.04.2023
- Impfdatum
- 31.03.2022
- Beginn
- 14.10.2022
- Tage bis Beginn
- 197,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Atrial flutter
Blood test
Echocardiogram
Electrocardiogram
Tachycardia
Symptomtext
I had taka cardia and atrial flutter Had a TEECG, I had the 2nd dose of the monkey pox vaccine a couple weeks prior. I am scheduled for an appointment in June to potentially have an atrial ablations
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tachycardia
- Hospital-Tage
- -
- Labordaten
- Blood test
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HIV, Hypertension, COPD
- Andere Medikamente
- Biktarvy: Duloxetine: Losartan:
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 06.03.2023
- Impfdatum
- 05.03.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 82,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Asthenopia
Blindness unilateral
Central nervous system lesion
Corrective lens user
Headache
Lumbar puncture
Magnetic resonance imaging abnormal
Migraine
Multiple sclerosis
Optic neuritis
Pain
Visual impairment
Symptomtext
I had my vaccination on 03/05/2022. On 05/26/2022 I had a headache that turned into a bad migraine. It started to affect my eyesight. Eye strain. It kept getting worse and were prescribed glasses. I lost my vision in my left eye. and then I went to the emergency room on 06/05/2022 as the pain was so bad. I had an MRI and Spinal Tap on 06/05/2022. I was diagnosed with Optic Neuritis in left eye and lesions throughout my brain. I was diagnosed with Multiple Sclerosis. I have ongoing medical appointments and I see the Neurologist 04/20/2023.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- 06/05/2022 MRI and Spinal Tap
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Endometriosis
- Andere Medikamente
- Simvastatin; Birth Control
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 01.03.2023
- Impfdatum
- 27.02.2022
- Beginn
- 15.08.2022
- Tage bis Beginn
- 169,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bronchitis
COVID-19
Condition aggravated
Diarrhoea
Fungal infection
Gastric disorder
Lung disorder
Malaise
Nasopharyngitis
Pain
Pancreatic failure
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Supraventricular tachycardia
Symptomtext
Felt like cold symptoms to start, achy and stopped up. Within 10 hours I had a 103-degree fever with TYLENOL. Went to urgent care to test. Doctor tested for COVID-19 with a PCR test, positive. Doctor prescribed amoxicillin, and monoclonal antibodies. Fever went down within 2 days but was still over 100. I was very sick for about 10 days, using a portable oxygen concentrator to keep O2 Sats up. The final 4 days symptoms gradually improved to basically non-existence. At about 21 days, sever bronchitis developed. Took a round of anti-inflammatory and antibiotics. Then the bronchitis returned for a second round of antibiotics. Then in October, there was an SVT event that did not result in hospitalization. By November all pulmonary functions returned to baseline. Also developed diarrhea that lasted into January. Exocrine Pancreatic Insufficiency and a yeast infection in the colon. Symptoms started with stomach problems exactly 90 days after the positive COVID-19 test.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- 16Aug2022 COVID-19 PCR positive
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Connective tissue auto immune; Sjogren's Syndrome; Hypertension; SVT; Type 2 diabetes; Hypothyroidism; Mixed Hyperlipidemia; Depression; Mild Emphysema; Interstitial lung disease; Glaucoma; Arthrosclerosis Seasonal Allergies; Hypo Magnesia; Irritable Bowel Syndrome.
- Andere Medikamente
- Hydroxychloroquine; diltiazem; JANUVIA; metformin; SYNTHROID; CYTOMEL; rosuvastatin; WELLBUTRIN; umeclidinium bromide; vilanterol; biotin; REPATHA; ZYRTEC; magnesium; probiotic; multivitamin; vitamin B complex; MIRALAX; COLASE
- Allergien
- Tetracycline; BACTRIM; clindamycin
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 28.02.2023
- Impfdatum
- 18.02.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 76,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Cardiac stress test abnormal
Chest X-ray abnormal
Drainage
Dyspnoea
Electrocardiogram abnormal
Hypertension
Left ventricular failure
Peripheral swelling
Symptomtext
I was out of town on a three-day trip and started having trouble breathing. My legs started swelling on the last day. I flew home and I went directly to the emergency room where they admitted me. They drained eight pounds of water off of me. They ran an EKG, chest x-ray, stress test. After staying in the hospital for three days I was discharged, I was given LASIX to take if I gained more than three pounds. I was also given losartan to take and diagnosed, with diastolic heart failure and high blood pressure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 3,0
- Labordaten
- EKG; Stress test; Chest X-ray
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Lupus; Sjogren's Syndrome; Reye's Syndrome
- Andere Medikamente
- Warfarin; pregabalin: trazadone; multivitamins; mycophenolate: sodium bicarb; bupropion; hydroxychloroquine; potassium tartrate; cevimeline; duloxetine; omeprazole; TYLENOL: tizanidine
- Allergien
- Vancomycin; methotrexate: IV contrast dye
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 06.02.2023
- Impfdatum
- 01.08.2022
- Beginn
- 01.11.2022
- Tage bis Beginn
- 92,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest pain
Dyspnoea
Productive cough
SARS-CoV-2 test positive
Upper respiratory tract infection
Symptomtext
In November when temperature change started having burning in chest shortness of breath and phlegm coming up diagnosed as upper respiratory infection. Lasted until 1st December. Prescribed doxycycline. Symptoms returned 12/12/2020 positive for Covid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Covid test 12DEC2022, Flu test 12DEC2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Afib; pancolitis
- Andere Medikamente
- Alfuzosin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 28.01.2023
- Impfdatum
- 25.02.2022
- Beginn
- 26.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Imaging procedure
Impaired self-care
Mobility decreased
Pain in extremity
Symptomtext
patient states that after she received the vaccine her upper arm was sore and that pain has affected how much she can raise her arm/move shoulder to the point of having difficulty getting dressed and washing back. She states that she went and saw a doctor a few months afterwards since the pain was ongoing. She said that they did some type of imaging and told her it was a problem with her muscle. she came in today looking for pain relief for arm (ongoing since her vaccine administration)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Some type of imaging when she saw her doctor when pain continued but was not sure the exact imaging done and did not provide an exact date
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none listed by patient or on her medication profile
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 08.12.2022
- Impfdatum
- 07.04.2022
- Beginn
- 30.11.2022
- Tage bis Beginn
- 237,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aspiration
Blood creatinine increased
Blood lactic acid
Blood urea increased
COVID-19
Clostridium test
Communication disorder
Computerised tomogram abdomen abnormal
Computerised tomogram thorax abnormal
Condition aggravated
Culture urine positive
Diarrhoea
Drug withdrawal syndrome
Dysphagia
Dyspnoea
Electrocardiogram normal
Endometrial thickening
General physical health deterioration
Symptomtext
Discharge Provider: MD Primary Care Provider: MD Admission Date: 11/30/2022 Discharge Date: Dec 6, 2022 COVID positive date: 11/30/2022 PRESENTING PROBLEM: Severe sepsis (HCC) Pneumonia due to organism HOSPITAL COURSE: Patient is a 70-year-old female with PMH significant for CVA (02/2015) with right-sided weakness, type 2 diabetes, gastroparesis, neuropathy, GERD, dyslipidemia, chronic lower back pain, dysphagia, major depression, vascular dementia (patient is a long-term resident and has a guardian presents to the hospital 11/30 due to AMS, dyspnea and a COVID diagnosed about 9 days prior to presentation. Patient had been slowly deteriorating, was noted to be hypoxic in the facility and was put on oxygen and was also noted to have decreased oral intake and decreased responsiveness. In ER she was febrile 38.6, tachycardic 139, tachypneic 25 and hypoxic she was also lethargic and not very communicative. Patient was started on broad-spectrum antibiotics Zosyn/vancomycin, imaging studies CT T/A/P showing-- bilateral airspace disease/pneumonia right greater than left, leukocytosis 14, BUN 36, creatinine 2, lactic acid 4.6 and procalcitonin 0.31. COVID test was positive. She was also noted to have a urinary tract infection. Patient had 1 bilious emesis and needed nasopharyngeal suctioning in ER. EKG without ST-T changes and patient admitted for severe sepsis. Patient admitted for severe sepsis related to pneumonia. Aspiration was suspected, SLP evaluated and resumed dysphagia diet. Dysphagia/aspiration precautions should continue. Zosyn/vancomycin was subsequently transitioned over to Rocephin/doxycycline to finish 5-6 day course. Symptomatically improved. Patient was able to wean down to room air. There was a suspected urinary tract infection at the time of presentation, cultures growing Proteus and Pseudomonas, however urinalysis itself was not impressive and urinary tract infection was felt to be ruled out. Patient subsequently had watery profuse diarrhea, C difficile was negative, was felt to be related to opioid withdrawal. Patient was noted to be on fentanyl patch chronically but not initially validated at admit and hence was not continued. This was resumed at half dosage at 25 mcg. Patient was noted to have low-grade vaginal bleeding, pelvic ultrasound showed endometrial thickening, requested following up with Gynecology as outpatient. I assumed care for the patient on day of discharge (12/6) - she felt well with improved breathing and denied any concerns including no difficulty with swallowing, chest pain, dyspnea, N/V, or abdominal pain. Pt had transport set up at 9:30 am per my colleague. Patient's glucose level was uptitrated. She is discharged in stable condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Dysphagia GERD (gastroesophageal reflux disease) Gastroparesis due to DM (HCC) Poor dentition Other constipation Leg pain Dementia (HCC) Chronic back pain Neuropathic pain DM (diabetes mellitus), type 2 (HCC) Late effects of CVA (cerebrovascular accident) Edema Insomnia Schizoaffective disorder (HCC) Osteoarthritis Major depressive disorder
- Andere Medikamente
- acetaminophen (TYLENOL) 500 MG tablet acetaminophen (TYLENOL) 500 MG tablet aluminum, magnesium & simethicone (MAALOX EX) 400-400-40 MG/5ML ARIPiprazole (ABILIFY) 2 MG tablet ascorbic acid (VITAMIN C) 500 MG tablet atorvastatin (LIPITOR) 80
- Allergien
- Bactrim [Sulfa Drugs] Hydrocodone Bitart (Antituss) [Hydrocodone] Hydrocodone-acetaminophen Trimethoprim Zofran [Ondansetron]
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 12.10.2022
- Impfdatum
- 07.04.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 78,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dyspnoea
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
On 06/24/2022 in the morning as soon as I woke up I had a runny nose. shortness of breath, and cough. The same day I tested positive. I went to the site to get care from the doctor who prescribed me with Paxlovid for 5 days. After 1 month of the medication my cough is back am not sure why. I contacted the doctor and they prescribed me with cough medicine. It didn't help with the cough. I am going to the doctor for my ongoing cough today 10/12/2022. I will be going to see an ENT for this issue as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 Test- Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure; Asthma; Shortness of breath; Anxiety
- Andere Medikamente
- Amlodipine; Aspirin; Omeprazole; Biotin; Vitamin B3; Magnesium; Flax Seed tablets
- Allergien
- None
- Vorherige Impfungen
- Dose 3 and 4 - Cough, headache, nausea and vomiting- 3 days
- Staat
- HI
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 02.09.2022
- Impfdatum
- 02.04.2022
- Beginn
- 09.04.2022
- Tage bis Beginn
- 7,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Hypoaesthesia
Myalgia
Paraesthesia
Symptomtext
Tingling and numbing feeling in the left and right feet and toes (4/9/2022 to 9/2/2022). Pins-and-needles and numbing feeling in the left and right legs (4/9/2022 to 9/2/2022). Pins-and-needles and numbing feeling in the middle section of body [front, sides, and back] (4/9/2022 to 9/2/2022). Joint and muscle pain (dull) in the right knee (4/9/2022-9/2/2022). Occasional muscle pain (dull) in the middle area of the lower back (4/9/2022-9/2/2022).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Valsartan, Chlorthalidone, Mometasone Furoate
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 14.04.2022
- Beginn
- 20.06.2022
- Tage bis Beginn
- 67,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amnesia
COVID-19
Cough
Dyspnoea
Fatigue
Malaise
Oropharyngeal pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I was sick for about 2 weeks. I was put on slightly higher doses of Prednisone along with cough pearls. I had cough, sore throat, congestion, fever of 101, shortness of breath, fatigue. I still have fatigue, shortness of breath and some memory loss issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- At home test- Positive PCR- June 20th, positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Asthma; Heart condition- heart attack in 2018; Transgender (hormone monitoring for long term hormone replacement risks)
- Andere Medikamente
- Zyrtec; Testosterone; Ditropanxl; Allexapro; Wellbutrin; Esomeprazole Magnesium; Vitamin D; Melatonin; Gabapentin; Famotidine; Prednisone; Albuterol
- Allergien
- Iodine; strawberries; Pineapple; Kiwi; Chloropropyl; Mercury; Formaldehyde; Ragweed; pollen; dust; Latex; Dog and cat dandruff; Avocadoes; Sulfate
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 06.07.2022
- Impfdatum
- 31.03.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Dyspnoea
Fatigue
Feeling abnormal
Nausea
Pain in extremity
Pyrexia
SARS-CoV-2 test positive
Visual impairment
Symptomtext
On the day after getting the dose 4, I woke up around 4:00 AM that morning and felt extremely fatigued and that lasted a couple days. Two days after dose for still extreme fatigue and very sore arm. On May 29th around dinner time I started feeling really bad and the next day it was worse so I went to the drive through testing site at a clinic and had a PCR test done. I had fever, nausea and also had vision problems like there was a film over my eyes that lasted around a week. I still am having some shortness of breath and low energy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- PCR COVID-19 test 06/01/2022 positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Protein supplement drink; ginger; multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 04.04.2022
- Beginn
- 14.06.2022
- Tage bis Beginn
- 71,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
COVID-19
Chills
Cough
Dyspnoea
Dyspnoea exertional
Fatigue
Feeling abnormal
Headache
Laboratory test normal
Myalgia
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID. Began June 14, 2022. Headache, muscle aches, fatigue, exhaustion chills, cough, shortness of breath, brain fog. Acute symptoms lasted approx 10 days with ongoing fatigue, exhaustion, poor stamina, some shortness of breath with exertion, brain fog with some decrease going on 22 days since start of virus.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Positive nasal swab tests on 6/14/22, 6/15/22, 6/16/22 and negative nasal swab test on 6/27/22. Also negative saliva test on 7/1/22.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Mild asthma
- Andere Medikamente
- Albuterol 2 puffs as needed
- Allergien
- Sensitivity to Clindimycin
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 05.07.2022
- Impfdatum
- 01.04.2022
- Beginn
- 21.05.2022
- Tage bis Beginn
- 50,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Dyspnoea
Lower respiratory tract congestion
Malaise
SARS-CoV-2 test positive
Symptomtext
I contracted COVID-19 on 05/21/2022 with symptoms of difficulty breathing, chest congestion, and slight cough. I was prescribed Paxlovid and an Albuterol inhaler on 05/23/2022. I was ill for 8 or 9 days before I recovered, but I had lingering symptoms of difficulty breathing. I am fully recovered now with no lingering symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 PCR test was positive on 05/23/2022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin D; Vitamin B12; Probiotic
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 30.06.2022
- Impfdatum
- 30.03.2022
- Beginn
- 03.06.2022
- Tage bis Beginn
- 65,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest discomfort
Dyspnoea
Exposure to SARS-CoV-2
Nasal congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
My husband initially tested positive for COVID-19 on 5/30/22. I took COVID-19 tests daily from 5/30/22-6/2/22 and they all came back negative. I woke up in the morning on 6/3/22 with nasal congestion. I thought it was allergies, so I started to gargle with salt water. The next day I woke up with a runny nose and I started to experience chest tightness, and my chest felt heavy as if someone was pushing on it. It was also hard to take in deep breaths. I took my oxygen level, and it was at 88. I took a COVID-19 test and it was positive. My husband called our primary care doctor and they prescribed me PAXLOVID. I took this medication from 6/5/22-6/10/22. My symptoms lasted for about 3 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- COVID-19 at home test on 6/4/2022 positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Osteopenia; High Cholesterol
- Andere Medikamente
- Rosuvastatin calcium; glucosamine chondroitin; flaxseed oil omega 3; chia seed oil omega 369; vitamin D3; turmeric extract; B12
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 16.05.2022
- Beginn
- 18.05.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test abnormal
Cellulitis
Confusional state
Dysarthria
Erythema
Hypotension
Lethargy
Posture abnormal
Sepsis
Skin weeping
Urinary tract infection
Urine analysis abnormal
Symptomtext
Became lethargic, leaning to right side. Confused. Low blood pressure. Slurring words. The thigh area had been reddened and weeping. Discussed with physician. Resident sent to hospital for eval and treat.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- 2,0
- Labordaten
- Blood work and urinalysis at the hospital 5/18/2022 indicated sepsis and urinary tract infection. Dx also with cellulitis at that time in thigh.
- Aktuelle Erkrankungen
- Gallbladder "sludge" and inflammation, cellulitis
- Vorgeschichte
- Diabetes, Glaucoma, Chronic Kidney Disease Stage IV, morbid obesity, hypertension, anemia, hyperlipidemia, insomnia, polyneuropathy
- Andere Medikamente
- Tylenol, Lactobacillus, Simvastatin, CoEnzyme Q10, Furosemide, Lanoprost eye drops, Levimir insulin, Melatonin, Miralax, Norco, Multivitamin, Vitamin D, artificial tears, calcium, debrox ear wax drops,
- Allergien
- Ibuprofen and Morphine
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Fatigue
Injection site erythema
Mobility decreased
Pain in extremity
Symptomtext
Patient states that adverse event began 6 hours post vaccination. Patient states she was unable to get out of bed even to use the bathroom. Patient states that her legs hurt so bad that they felt "broken". Patient experienced extreme fatigue in addition to the lower limb pain. Patients right arm did become red from shoulder to elbow and has recovered to approximately 2 inch diameter redness at 1 week post vaccination. Patient denies any fever post vaccination. Patient did not take any pain medication during event. Patient did not follow up with doctor or vaccination clinic regarding these events until 5/12/22, seven days post vaccination, where she discussed with pulmonologist at pre-scheduled appointment. Patients symptoms have resolved as of date of report. Patient states that previous doses of vaccine did not cause any adverse events. Patient has never had adverse event prior to this with any other vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- CHRONIC LYMPHOGENOUS LUKEMIA, HYPERTENSION, DIABETES, HYPERLIPIDEMIA
- Vorgeschichte
- -
- Andere Medikamente
- CENTRUM, JANUMET, ASA 81MG, PLAVIX,CARVEDIOLOL, REPAGLINIDE, COLACE, HYDROXYZINE, DULOXETINE
- Allergien
- JARDIANCE, FARXIGA, SULFA ANTIBIOTICS, PENICILLIN
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 08.02.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 34,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Back pain
Blood calcium decreased
Blood test abnormal
Chest X-ray normal
Erythema
Fluid retention
Genital erythema
Hypoaesthesia
Lacrimation increased
Magnetic resonance imaging normal
Muscle strain
Muscular weakness
Musculoskeletal pain
Pain in extremity
Palpitations
Paraesthesia
Peripheral coldness
Symptomtext
He got his vaccine, he was fine for 5-6 weeks. When he first went to the doctor his toes were red, and her fingers were turning red. They were cold, his feet were cold and his hands were cold. 2nd visit, he went back as his right calf was pulling real hard like a muscle was pulled, but he did not do anything to it. They did blood work and said that he was low on calcium and that everything else looked fine. She was supposed to order an MRI, but was waiting for it and they switched clinics. Two weeks later he got up his hands were red, his heart was racing and he called an ambulance. He went to the ER, they did a chest x-ray, was worried about his heart and they did 3 sets of blood work and said that everything was fine. He asked why his hands were read and they could not tell him. After that he went back to the doctor, told her that he went to the ER and then she said that they were going to get an MRI. He went to the hospital again as his hands were turning red, his left hand was turning red/purplish, he was loosing feeling in his left arm. He took the bus, made it 3 blocks away from the hospital and called for an ambulance and went to the hospital. When he went there his genitals were red, his feet were more red too and his hands were red. He was there for about 15 hours, they did blood work, took an X-ray, did an MRI as he was worried there was a blood clot and there is not. He then went home and after that his skin was fine, the redness went away and was back to normal again, this was a week ago. Now his hands are bright red again, his feet are cold, was having tingling in his feet and hands. Then his genitals turned red again. Where he got the shot from on the left side, his arm was getting weak as it is now again and seems to be repeating the same feeling over and over again. When he is sleeping he had a pain in his butt cheek, like a sciatic nerve was going off, which he could not figure out why. Now the pain in his calf is gone, and now his feet he still has on the toes some tingling, but his hands are red and feels like it going past his wrist on his arm. He went to the hospital again yesterday due to the redness of his genitals and they are still that color again, and was informed that it takes about 24 hours and they are still red, but is worried about the redness in his hand moving up his arm. He felt as if he was retaining water, took one of his wife's diuretics and was told by the doctor not to take any more. When he went to the ER it was his right arm that was weak, and the left arm was getting strong again, and now it's opposite. He also has some pain going up his back that leaves real quick. Feels that it must be from the booster shot as there is nothing wrong with him. His wife is handicapped and he takes care of her, eats right and is concerned of the redness. His neck is also a little weak and having tearing in his left eye. He just wants to know if this is a reoccurring thing, has to wait for it to go through and if he's going to be okay. He had COVID on 1/31/22, thought he had a cold and did a COVID test and was positive. He stayed quarantined for the 14 days, and then decided to get the booster to protect his wife who is learning how to walk again. Then 6 weeks later has been having the symptoms he has been having and it just seems to be recurring, and every day it seems to be something else. During the day his hands feel tight and at night they release and go back to normal again, and cannot figure out what is going on and if it's going to affect his heart or his lungs and that he is never sick. He has not had any issues like this prior to the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- As above.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure.
- Andere Medikamente
- Losartan Potassium 100 mg once a day, Atorvastatin 20 mg once daily, Health fungus eliminator 2 capsules a day.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 22.04.2022
- Impfdatum
- 15.03.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Gait disturbance
Loss of personal independence in daily activities
Mobility decreased
Myalgia
Pain
Symptomtext
For 3 days following my Cov19 Moderna booster vaccine I experienced strong muscle aches and pains that made it difficult for me to get out of bed and walk and do things for the day. I saw no dr for this and had no tests or treatments for this. After 3 days the problems went away and I was good good as I was before the booster vaccine and had no further problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Ulcerative colitus, diabetes type 2, glaucoma both eyes, high blood pressure
- Andere Medikamente
- Low dose aspirin, complete multivitamin for men 50+, amlodipine besylate 2.5 mg tab, lisinopril hctz 20-12.5 mg tab and novolin 70/30 35 units
- Allergien
- Only allergic to zyban
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 22.04.2022
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthma
Bronchospasm
Condition aggravated
Dysphonia
Oxygen saturation decreased
Wheezing
Symptomtext
She got her vaccine, she waited 15-20 minutes after the injection, went home and went about her daily activities with no problems, no wheezing or anything. About 8-8:30 last night she began with wheezing that became more severe and then had bronchospasm. Because she is asthmatic she keeps a pulse ox and peak flow meter and it was trending down, lowest 85. She gave her 3 nebulizer treatments and took 30 mg of Prednisone. Basically tried to stay calm and everything reversed when her Sp02 came back to 95 or so and this took about 12 hours to normalize. She was able to fall asleep on 3 pillows, and this morning her voice is hoarse and has a little bit of wheezing left. She contacted her pulmonologist and he has put her on a course of Prednisone and to use her nebulizer every 4-6 hours as necessary. She has not had an asthma attack like this in over 15 years. She has the things to treat it at home, but was within 15-20 minutes of considering going to the hospital but it began turning around. The vaccine was the only thing that was different that day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Asthma, prediabetes, atrial fibrillation, obesity.
- Andere Medikamente
- Omeprazole, Januvia, Lisinopril, Eliquis, Brio inhaler 200/25, Fluticasone nasal spray.
- Allergien
- Codeine, opioids with anaphylaxis reactions; Sulfa, Doxycycline, Tetracycline (rash reactions to those).
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Decreased appetite
Lethargy
Malaise
Mobility decreased
Movement disorder
Myalgia
Pain
Pyrexia
Symptomtext
Extreme lethargy, extreme body pain, could not move, high fever that wouldn't go down with tyenol or ibuprofen, muscle aches, joint pain, loss of appetite, unable to lift arm, very sick to stomach. Sickest I have been in years.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- -
- Andere Medikamente
- Monograph, aldosterone receptor antagonists, multi vitamin, alpha lipolic acid, fish oil, green tea
- Allergien
- N/A
- Vorherige Impfungen
- Raised bumpy rash from yellow fever vaccine 2016
- Staat
- TX
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Dyspnoea
Feeling hot
Flushing
Hyperhidrosis
Symptomtext
Systemic: Allergic: Difficulty Breathing-Mild, Systemic: Chest Tightness/Heaviness/Pain-Mild, Systemic: Flushed/Sweating-Mild, Additional Details: Within 2 minutes after administration patient alerted pharmacist she felt out-of-breath, chest tightness and an overall warm feeling. At 5 minutes, blood pressure and heart rate checked with arm blood pressure kit. All numbers were normal. At this time, patient felt a little better. At 10 minutes, I offered Benadryl and/or Zyrtec but patient declined. She stated she felt much better. She could go home with no issues.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 16.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Arthralgia
Asthenia
Blood pressure increased
Brain natriuretic peptide
Chest pain
Decreased appetite
Differential white blood cell count
Dizziness
Dyspnoea
Exercise tolerance decreased
Fatigue
Fibrin D dimer
Full blood count
Headache
Heart rate increased
Injection site pain
Metabolic function test
Nausea
Symptomtext
Beginning 4/12/22: Pain and tenderness at injection site, headache, nausea, arthralgia, inappetence, fatigue, lightheadedness, weakness, fever (39.1?C) Beginning 4/14/22: Elevated heart rate, elevated blood pressure, palpitations, chest pain, fatigue, weakness, lightheadedness, exercise intolerance, shortness of breath
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- BNP, CBC/PLT/DIFF, Comp Metabolic Panel, D-DIMER Quant, Troponin I
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- CAD, sleep apnea, hypothroidism, GERD, osteoarthritis, ADD, atrial fibrillation
- Andere Medikamente
- Atorvastatin, Metoprolol, Levothyroxine, Pantoprazole, Pradaxa, Lisinopril, Aspirin, Adderall, Nitroglycerin, Valerian root, Vitamin D3, Vitamin B complex, Claritin, Alvesco, Flonase
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 13.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Hypoaesthesia
Immediate post-injection reaction
Injected limb mobility decreased
Injection site pain
Limb injury
Pain in extremity
Paraesthesia
Symptomtext
Site: Pain at Injection Site-Severe, Systemic: patient reported immediate pain upon vaccination and has since reported decreased use of left arm and continuing pain in arm-Severe, Systemic: Numbness (specify: facial area, extremities)-Severe, Systemic: Weakness-Severe, Error: Shoulder Joint Injury (prolonged pain, tingling, etc.)-, Additional Details: patient reported pain at injected arm as well as limited mobility of arm and decreased strength in arm
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 09.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Chest pain
Symptomtext
Systemic: Chest Tightness / Heaviness / Pain-Severe, Additional Details: Patient received his second Moderna booster (0.25ml) around 12 noon on 3/31/22. Patient said he experienced "bad" chest pain that started later that night and into the next day (4/1/22) and resolved on 4/2/22. He said the chest pain on 4/2/22 was mild. Patient said he spoke to his primary prescriber via phone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 01.04.2022
- 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
Feeling cold
Impaired work ability
Lethargy
Mobility decreased
Tremor
Symptomtext
Approx 22 hours after receiving the shot, started feeling lethargic, cold, shaking uncontrollably, patient left work. At home the temperature was 103.5 F. Stayed in bed that day, used ice, tylenol 500mg to decrease temperature. Stayed in bed for 3 days. Able to get up 3 days later on April 4th. Maintained fluids with care from husband.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- osteoporosis, high blood pressure, mild arthritis in hip
- Andere Medikamente
- hctz 25mg daily, tizanidine 4mg as needed, calcium citrate 200mg three times daily, amlodipine 10mg daily, ibuprofen 800mg as needed, hydrocodone 5/325 1/2 tab twice daily, restasis eye drops, multivitamin daily, lo dose asa in the evening
- Allergien
- no known
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 82,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tremor
Symptomtext
Per Dr.'s office representative: Tremors/shaking (Parkinson-like) that began within one hour of vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Iodine, Methylprednisolone, Shellfish-derived products
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- UNK
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chills
Condition aggravated
Extra dose administered
Headache
Influenza like illness
Myalgia
Tremor
Symptomtext
The usual initial symptoms started around 12 hours after injection; severe flu like symptoms, chills, joint/muscle aches, headache. I get those all after every Moderna injection. This was my 2nd booster. I had severe peripheral tremors after my hospitalization with COVID in November 2020 but they were improving significantly. They did not return/worsen after any of the previous 3 vaccinations I received. Three days after this injection, most flu symptoms were subsiding or gone but I started having trouble with my tremors worsening. By Monday (5 days) they were severe, similar to what I had immediately after my hospitalization so I sealed medical attention.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Slight peripheral tremors as a result of severe COVID infection and hospitalization 15 months previously
- Andere Medikamente
- Super B Complex D3
- Allergien
- NSAIDs, shellfish
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 01.04.2022
- Impfdatum
- 30.03.2022
- Beginn
- 30.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain
Pain in extremity
Paraesthesia
Peripheral swelling
Symptomtext
PATIENT STATED EXTREME PAIN IN ARM WITH SWELLING AND TINGLING DOWN ARM AND IN HAND. SAYS ARM HURTS WHEN IT HANGS BUT FEELS BETTER WHEN STABLIZED. CAME INTO PHARMACY 2 DAYS AFTER VACCINATION AND STATED STILL HURTS BUT NOT AS BAD AS FIRST DAY. SAID ALL HE TOOK WAS 2 BC POWDERS FOR PAIN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 02.03.2022
- Beginn
- 05.03.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Influenza like illness
Palpitations
Symptomtext
I have been having ongoing heart palpitations for 3.5 weeks, since during/shortly after the flulike symptoms from my booster wore off. They are consistent throughout the day and night, coming and going, increasing with activity, especially if I raise my arms up over shoulder height. I *may* be experiencing very mild shortness of breath, but it?s hard to say because the palpitations are so pronounced that they might be what I?m feeling. I have an appointment with a cardiologist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- I have had a history of SVT (superventricular tachycardia), diagnosed at age seven, but it?s tolerated and untreated as symptoms are very rare.
- Andere Medikamente
- Isotretinoin (once weekly) Tylenol after vaccination to help with flu-like side effects
- Allergien
- None
- Vorherige Impfungen
- I threw up once after a flu shot.
- Staat
- TN
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- 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
Arrhythmia
Headache
Heart rate
Pyrexia
Symptomtext
This spontaneous case was reported by a consumer and describes the occurrence of ARRHYTHMIA (during the night, approximately 1 and a half hour after fever started, patient started to experience a rapid irregular heart beat) in a 55-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Penicillin allergy, Latex allergy, Multiple sclerosis (The patient did not have any change in status such as improvement or worsening.) since 1995, Heart disorder, Stomach function disorder and Arrhythmia (it was a problem since a few years ago, even before the vaccine was given). Concomitant products included PANTOPRAZOLE for Stomach function disorder, OCRELIZUMAB (OCREVUS), GABAPENTIN, ROPINIROLE, BACLOFEN, BUPROPION HYDROCHLORIDE (WELLBUTRIN), DIAZEPAM, HYDROCHLOROTHIAZIDE, TRIAMTERENE (TRIAMTERENE & HCTZ), DICYCLOMINE [DICYCLOVERINE], PROMETHAZINE and MELOXICAM (MOBIC) for an unknown indication. On 17-Mar-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Mar-2022, the patient experienced ARRHYTHMIA (during the night, approximately 1 and a half hour after fever started, patient started to experience a rapid irregular heart beat) (seriousness criterion medically significant), HEADACHE (experienced again headache) and PYREXIA (very high fever). The patient was treated with ACEBUTOLOL ongoing since an unknown date at an unspecified dose and frequency; PARACETAMOL (TYLENOL [PARACETAMOL]) at an unspecified dose and frequency and IBUPROFEN at an unspecified dose and frequency. On 17-Mar-2022, ARRHYTHMIA (during the night, approximately 1 and a half hour after fever started, patient started to experience a rapid irregular heart beat) and PYREXIA (very high fever) had resolved. At the time of the report, HEADACHE (experienced again headache) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 17-Mar-2022, Heart rate: rapid irregular heart beats (abnormal) rapid irregular heart beats. The patient did not have a history of Myocarditis/pericarditis. The patient never had COVID positive test or diagnosis. The patient did not receive any other vaccines within 1 month prior to Moderna COVID-19 vaccine. The patient mentioned she experienced rapid irregular heart beats even before getting any of the vaccines, because she had heart problems; but this time, when she took her medication (Acebutolol) to control it, it got worse, for approximately 3 hours. The patient still had a bit of headache. As per the patient the rapid irregular heart beats was related to booster dose. There were no cardiac lab values (ECG, cardiac test, cardiac enzymes) and the cause was not determined. The adverse events did not cause the patient to seek medical care (office visit, urgent care, ER, hospitalized). The patient had rapid irregular heart beats even after 3rd dose also. Company Comment: This spontaneous case concerns a 55 year old female with relevant medical history of multiple sclerosis (stable condition), heart disorder and cardiac arrhythmia, who experienced serious (medically significant), unexpected, AESI event of arrhythmia which occurred on the same post vaccination with the booster dose (4th dose) of mRNA-1273 vaccine. On the same day post vaccination with the booster dose of mRNA-1273 vaccine (4th dose) this patient experienced non-serious, expected events of headache and pyrexia. This patient was treated with Acebutolol and paracetamol. The patient did not seek any medical care (office visit, urgent care, ER, hospitalized) and also no laboratories /diagnostic procedures were reported. This patient had low grade fever after the first two doses of mRNA-1273 vaccine which resolved spontaneously as well as for the third dose however for the third dose it was continuous and needed medication and resolved after 3 days. So for the event of pyrexia it is positive re-challenge. Event of arrhythmia, headache and fever was also reported for the 3rd dose of the mRNA-1273 vaccine hence possible positive re-challenge for the event headache, fever and arrhythmia. The outcome of the event arrhythmia and fever is resolved. And for the event headache it is resolving. The above medical history of Cardiac arrhythmia, cardiac disorder and multiple sclerosis are considered as confounders for the event arrhythmia while for the event of fever and headache her medical condition of multiple sclerosis is a confounder. The benefit -risk relationship of mRNA -1273 (Moderna Covid-19 Vaccine) is not affected by this report. This case was linked to MOD-2022-517635, MOD-2022-517697, MOD-2022-517699 (Patient Link). Sender's Comments: This spontaneous case concerns a 55 year old female with relevant medical history of multiple sclerosis (stable condition), heart disorder and cardiac arrhythmia, who experienced serious (medically significant), unexpected, AESI event of arrhythmia which occurred on the same post vaccination with the booster dose (4th dose) of mRNA-1273 vaccine. On the same day post vaccination with the booster dose of mRNA-1273 vaccine (4th dose) this patient experienced non-serious, expected events of headache and pyrexia. This patient was treated with Acebutolol and paracetamol. The patient did not seek any medical care (office visit, urgent care, ER, hospitalized) and also no laboratories /diagnostic procedures were reported. This patient had low grade fever after the first two doses of mRNA-1273 vaccine which resolved spontaneously as well as for the third dose however for the third dose it was continuous and needed medication and resolved after 3 days. So for the event of pyrexia it is positive re-challenge. Event of arrhythmia, headache and fever was also reported for the 3rd dose of the mRNA-1273 vaccine hence possible positive re-challenge for the event headache, fever and arrhythmia. The outcome of the event arrhythmia and fever is resolved. And for the event headache it is resolving. The above medical history of Cardiac arrhythmia, cardiac disorder and multiple sclerosis are considered as confounders for the event arrhythmia while for the event of fever and headache her medical condition of multiple sclerosis is a confounder. The benefit -risk relationship of mRNA -1273 (Moderna Covid 19 Vaccine) is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220317; Test Name: heart beats; Result Unstructured Data: rapid irregular heart beats.
- Aktuelle Erkrankungen
- Arrhythmia (it was a problem since a few years ago, even before the vaccine was given); Heart disorder; Latex allergy; Multiple sclerosis (The patient did not have any change in status such as improvement or worsening); Penicillin allergy; Stomach function disorder.
- Vorgeschichte
- -
- Andere Medikamente
- Ocrevus; Gabapentin; Ropinirole; Baclofen; Pantoprazole; Wellbutrin; Diazepam; Triamterene & HCTZ; Dicyclomine [Dicycloverine]; Promethazine; Mobic
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 28.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain upper
Asthma
Condition aggravated
Contusion
Diarrhoea
Headache
Insomnia
Pyrexia
Rash
Symptomtext
I developed a abdominal rash, and got diarrhea it was uncontrollable and stomach aches. I got a rash across my abdomen and had to call my doctor because the rash was so bad it was bruising me.I have been having headache and fever. My asthma has gotten worse since, I am having acute asthma attacks. I have been put on steroids' and antibiotics and have been referred to a pulmonologist to see what is going on. I am unable to go anywhere without my rescue inhaler. I now have to sleep sitting up because my asthma has gotten so bad since my 3rd dose. My asthma is just worse
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma , Thyroid Tumors being monitored, and Depression
- Andere Medikamente
- Levothyroxine 100mg 2am, Hydrochlorothiazide 12.5mg, Bupropion SS100mg, Montlucalve 10mg HS, Brio Ellipta , Fluticasone 1 spray am, Azelastine Nasal Spray, Albuterol Neb, every 6 hours, Proair Rescue Inhaler every 4 hours, QVar Inhaler 4
- Allergien
- Sensitive to Codeine
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 23.03.2022
- Beginn
- 24.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Back pain
Chest discomfort
Chest pain
Chills
Dyspnoea
Headache
Heart rate increased
Heart rate irregular
Hyperhidrosis
Immediate post-injection reaction
Injection site pain
Nasal congestion
Pain
Pharyngeal swelling
Pyrexia
Swelling face
Symptomtext
Immediately after the shot : shocking headache in the middle of the head nothing too bad. Began with chills, and fever. At 12am. 12:30 started to sweat and body aches 1am stuffy nose and face starting to swell along with my throat. Rapid irregular heart beat, chest pain, shortness of breath, impending doom Still have some chest tightness, injection site pain, and sore back muscles but everything else has subsided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None I'm too poor to go to the hospital right
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Irritable Bowel Syndrome
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Bone pain
Chills
Cough
Dyspnoea
Fatigue
Gait disturbance
Headache
Hyperhidrosis
Injection site erythema
Injection site rash
Nasal pruritus
Nausea
Pain
Pain in extremity
Productive cough
Pyrexia
Symptomtext
She got her vaccine, started around 7:30 and 8:00 AM next morning started off with a headache, and then chills, then a fever. When she got up to go walk every bone and joint in her body was aching, difficulty walking, and fingers were hurting. She went to the bathroom, started taking Tylenol. Then she had started up with a cough and now it's like a post nasal drip cough and spitting up phlegm. She has also been nauseous ever since then. She broke out with a bad rash around the injection site, got real real red, but is lightening up today. Very itchy nose. She also has weakness, everything she tries to do is a task. Her breathing is like light winded, has to take a deep breath to try to breath, also maybe due to the nausea and the weakness. She has been taking Alka Selzer plus cold and cough. She contacted the pharmacy who told her that they were going to report her symptoms to the CDC, and is reporting herself as she is having more symptoms and how long are they going to last. She has been breaking out into sweats and woke up last night drenched and had to change the sheets as they were soaked as well. She has also been having severe pounding headache, and when she coughs she has to hold her head as the headache is so bad, and moving her head in the bed is painful as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Depression, anxiety, blood pressure.
- Andere Medikamente
- Venlaflaxine 150 mg once a day, Ativan 1 mg once a day, Latuda 20 mg once a day, Wellbutrin 150 mg once a day, Amlodipine 5 mg once a day.
- Allergien
- Latex, Phenytonin, Depakote, Tegretol, Trileptal, Amytriptyline, Lamictol, Zyprexa, Combipatch (adhesive to it).
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 18,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspnoea
Symptomtext
DIFFICULTY BREATHING, ALUBUTEROL INHALER, EMS TOOK PT TO HOSPITAL
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- ASTHMA
- Andere Medikamente
- PROAIR, MEDROL DOSEPAK, IBUPROFEN, PROMETHAZINE DM
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- Impfdatum
- 14.03.2022
- Beginn
- 14.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Dizziness
Hypoaesthesia oral
Paraesthesia oral
Symptomtext
After getting vaccine, patient waited for any reactions. Patient started feeling dizziness, chest tightness, numbness and tingling around the mouth. Patient was taken back and took vitals. Healthcare provider examined patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 02.03.2022
- Beginn
- 02.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- UN / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Headache
Joint stiffness
Muscle tightness
Tinnitus
Symptomtext
Tinnitus . Also reports headache, neck and shoulder tightness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Hearing loss and tinnitus from second dose. Now wears hearing aide.
- Aktuelle Erkrankungen
- unk
- Vorgeschichte
- PUD, obesity, connective tissue disease, sleep apena, gerd, ulcer, hearing loss, anxiety, RA, hypertention, hypothyroidism,
- Andere Medikamente
- adalimumab, clobetasol, estradiol, flonase, folic acid, hctz, ibuprofen, mirena, levothyroxine, lisinopril, ativan, methotrexate, MVI, tramadol.
- Allergien
- nkda.
- Vorherige Impfungen
- Tinius and hearing loss after Moderna 2nd dose.
- Staat
- IL
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adverse reaction
Chills
Dizziness
Dyspnoea
Nausea
Pain
Tachycardia
Symptomtext
Adverse reaction to Moderna covid booster with dyspnea, rigors, nausea and dizziness today. Had simliar symptoms with previous 2 covid vaccine doses. Prior 2 doses Pfizer vaccine. Known anaphylacitc reactions in the past to unclear triggers (gluten, mint, hibiscus, skin products). Notes allergist believes she may react to preservatives in food. Lungs clear to auscultation, good air entry on exam. - Observed in clinic until symptoms resolved; patient declined to be transported to ED - Vitals stable throughout reaction, oxygen saturation >95%, normotensive, intermittently tachycardic while in pain though recovers quickly - Completed albuterol nebulizer treatment with improvement - Declined epipen or prednisone; preferred to take own benadryl she brought with her - Encourage hydration given rigors and muscle pain - Discussed warning signs, when to present to ED, patient voiced understanding - Caution with further covid vaccines, has not had reaction to 3 of 3 doses, 2 different brands - Encourage follow up with allergist to narrow down potential allergens
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- allergic rhinitis anxiety disorder asthma attention deficit hyperactivity disorder, predominantly inattentive type bipolar I disorder celiac disease chronic interstitial cystitis concussion injury of brain eczema gastroesophageal reflux disease irritable bowel syndrome obsessive-compulsive disorder posttraumatic stress disorder spondyloarthritis
- Andere Medikamente
- Aczone Advair HFA albuterol sulfate alprazolam amitriptyline azelastine cyclobenzaprine Elmiron epinephrine Flonase Allergy Relief hydroxychloroquine lithium carbonate metronidazole montelukast ondansetron HCl prednisone propranolol sulfasa
- Allergien
- cat dander coconut dog dander gluten house dust
- Vorherige Impfungen
- States she had similar reaction with previous doses COVID 19 vaccine; Pfizer given 4/2021 and 5/2021. They were given elsewhere.
- Staat
- NC
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 13.02.2022
- Beginn
- 13.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Fatigue
Headache
Mobility decreased
Nausea
Somnolence
Symptomtext
Chills, severe headache, nausea, feeling of almost passing out, very tired. Slept in bed for 2 days, took ibuprofen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Levothyroxine; 8 in 1 immune defend vitamin; Vitamin D3.
- Allergien
- Sulfa.
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 04.04.2023
- Impfdatum
- 01.04.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 104,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Decreased appetite
Fatigue
Headache
Malaise
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
My COVID-19 symptoms started on 07/14/2022 in the morning . I had a sore throat, fatigue , loss of appetite, fever, and headaches. I did a home test on the same day which was positive. I called my doctor right away. He prescribed me Paxlovid for 5 days. I took Tylenol for fever and my regular medication. I completely recovered from COVID-19 infection within 3 weeks. I was sick for 2 weeks.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 14JUL2022 COVID-19 Test- Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; Obesity
- Andere Medikamente
- Hydrochlorothiazide; Magnesium Supplements
- Allergien
- Amlodipine
- Vorherige Impfungen
- COVID-19 vaccines- Headache, sore arm and lethargic for 24 hours
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 03.04.2023
- Impfdatum
- 01.04.2022
- Beginn
- 22.02.2023
- Tage bis Beginn
- 327,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Diarrhoea
Eye irritation
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
It started off with sore throat, burning eyes, diarrhea. I tested positive with COVID-19 on 02/22/2023. I had a telehealth with my provider on 02/22/2023 and prescribed PAXLOVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- 22FEB2023 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Type 2 Diabetes; Hypertension
- Andere Medikamente
- Metformin; lisinopril; atorvastatin; amlodipine; DESCOVY
- Allergien
- Contrast dye
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 06.03.2023
- Impfdatum
- 03.03.2022
- Beginn
- 12.10.2022
- Tage bis Beginn
- 223,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Blood bilirubin increased
Blood test
Malaise
White blood cell count decreased
Symptomtext
Low white blood cell count: High belly Reuben: generally, wasn't feeling well low energy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- Blood
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Multivitamin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 20.10.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Somnolence
Vaccination site pain
Symptomtext
Made patient sleepy; Injection site left arm soreness; This spontaneous case was reported by a patient family member or friend and describes the occurrence of SOMNOLENCE (Made patient sleepy) and VACCINATION SITE PAIN (Injection site left arm soreness) in a 72-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 31-Mar-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 31-Mar-2022, the patient experienced SOMNOLENCE (Made patient sleepy) and VACCINATION SITE PAIN (Injection site left arm soreness). At the time of the report, SOMNOLENCE (Made patient sleepy) and VACCINATION SITE PAIN (Injection site left arm soreness) outcome was unknown. No concomitant drug was reported. No treatment drug was reported. This case was linked to MOD-2022-660901 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 06.10.2022
- Impfdatum
- 05.04.2022
- Beginn
- 02.08.2022
- Tage bis Beginn
- 119,0
- Dosis
- N/A
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Body temperature increased
COVID-19
Chills
Cough
Headache
Malaise
Oropharyngeal pain
Pain
SARS-CoV-2 test positive
Sneezing
Symptomtext
Contacted Covid19. High Temp, Sore Throat, Chills, Aches, General Not Feeling Well, Sneezing (significant), Dry Cough, Headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Covid 19 test administered and return positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HIV+ undetectable
- Andere Medikamente
- Biktarvy, Saw Palmetto, Multi Vitamin, Lunesta, Naproxen, Zyrtec, Benadryl
- Allergien
- Sulfa, Bee Stings
- Vorherige Impfungen
- Feeling unwell after previous Covid 19 vaccines, Flu Vaccine causes temporary unwell feeling
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 03.10.2022
- Impfdatum
- 01.04.2022
- Beginn
- 09.08.2022
- Tage bis Beginn
- 130,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Malaise
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I had a sore throat and a fever of 102. I tested negative for COVID-19 on the first day. Then I tested the next day and was positive. It was a mild case. I talked to the nurse and I was prescribed me PAXLOVID. My symptoms lasted for 4-5 days but test positive for 8 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- COVID-19 test; 08/09/2022, negative. COVID-19 test; 08/10/2022, positive.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Prostate Cancer; Heart Disease
- Andere Medikamente
- LIPITOR; losartan; bicalutamide; carvedilol; low dose aspirin; vitamin D; magnesium chloride; calcium
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 30.09.2022
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Influenza like illness
Injection site pain
Injection site swelling
Nasopharyngitis
Pain
Symptomtext
I had swelling and soreness at the injection site that evening I had flu like symptoms cold and achy needing to drink warm fluids this lasted for two days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- No.
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- Asthma; Breast Cancer
- Andere Medikamente
- SINGULAIR; albuterol; triamcinolone ointment; betamethasone; exemestane; vitamin B complex; vitamin B2; vitamin D; vitamin C
- Allergien
- Penicillin; latex; cashews; eggs
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 24.08.2022
- Impfdatum
- 24.05.2022
- Beginn
- 10.07.2022
- Tage bis Beginn
- 47,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Fatigue
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
I had a bad cough; chest congestions; no fever; tired; exhausted. I tried to take MUCINEX for the chest congestions for few days till I contacted my doctor. On 07/14/2022 I did a telehealth with my doctor. He prescribed me with PALOVID for 5 days. I started feeling better after taking the medication. On the 5th day I tested negative. I still have lingering cough.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- COVID-19 test - positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Heart disease; Seasonal allergies
- Andere Medikamente
- ELIQUIS; propanone; simvastatin; carvedilol; lisinopril; omeprazole; multivitamin; calcium; magnesium; potassium; B12; hair skin and nails; coQ10
- Allergien
- Sulfa; NAPROSYN; hydrocodone
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 24.08.2022
- Impfdatum
- 24.05.2022
- Beginn
- 04.07.2022
- Tage bis Beginn
- 41,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Oropharyngeal pain
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
On 6-29, I left on a cruise ship traveling domestically. On 7-4-2022, I started having a sore throat and cough. These symptoms continued and on 7-7, I went to the cruise ship's medical office and tested positive for COVID-19. I went in to isolation on the ship. I returned home on 7-9 and did not go to see a doctor. I did text my doctor letting them know that I tested positive. He stated to ride it out and no medications or tests were performed. I am reported my breakthrough case of COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- 7-7-2022 COVID-19 test with positive results.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension; Diabetes
- Andere Medikamente
- Aspirin; atorvastatin; glipizide; hydrochlorothiazide; losartan; metformin; multivitamin; niacin
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 23.08.2022
- Impfdatum
- 20.02.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Impaired work ability
Malaise
Nasal congestion
Oropharyngeal pain
SARS-CoV-2 test positive
Symptomtext
On 02/20/2022, I received my second Moderna booster for COVID-19. On the night of 4/22/2022, I woke up a couple of times with a sore throat. On 4/23/2022, the sore throat resolved itself, and I had no symptoms during the day. During that night, though, the sore throat returned. When I woke up on 4/24/2022, I had both a sore throat and a stuffy nose. I did an at-home test for COVID-19, which yielded a positive result. I then took a PCR test at a drive-thru site later that day, and it also yielded a positive result. My symptoms were the worst on 4/25/2022, 4/26/2022, and 4/27/2022. On those days, I had sore throat, coughing, stuffy nose, extreme fatigue, and general malaise. I had a telehealth visit with my doctor on 4/25/2022, and she prescribed me a 5-day course of Paxlovid. After 4/27/2022, I began to feel better, though the cough did linger a bit. With that being said, though, it wasn't a severe cough. The fatigue was also pretty much gone by 4/30/2022. On 5/2/2022, I was able to return to work, though I wore a mask the entire time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 4/24/2022--Home COVID-19 Test--Positive Result; 4/24/2022--PCR Test--Positive Result.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Possible Crohn's Disease; Rectal-Vaginal Fistula.
- Andere Medikamente
- Remicade; Estradiol Cream; Estradiol Pills; Multivitamin.
- Allergien
- Amoxicillin; Poison Ivy; Cat Dander.
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 29.07.2022
- Impfdatum
- 30.03.2022
- Beginn
- 26.07.2022
- Tage bis Beginn
- 118,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Eye pruritus
Lymphadenopathy
Pruritus
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I still have the symptoms which have been very mild but I'm getting better. I'm on PAXLOVID. I thought it was an allergy because I had a runny nose and dry cough. Also with itchy eyes and ears. My head is less stuffed up. I also had a huge swollen lymph node on the same side of the injection site on my neck after the vaccine that appeared 1 day after. It lasted for about a month. On the 20th of July I had the Tdap vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Eye pruritus
- Hospital-Tage
- -
- Labordaten
- COVID-19 at home - positive on 7/27/22 AM.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Vitamin C; B complex; low dose aspirin
- Allergien
- No
- Vorherige Impfungen
- After 3rd Pfizer I had a huge swollen lymph node on the same side of the injection that lasted for about a month.
- Staat
- WA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 25.07.2022
- Impfdatum
- 15.04.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 89,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anxiety
COVID-19
Chest X-ray
Electrocardiogram
Influenza like illness
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
I started feeling like a runny nose on Wednesday. It got worse on Thursday And on Friday it got worse I started feeling like I was running a fever and flu like symptoms. I took an at home test and went to see my doctor to get Pavloxid. Urgent care was worried about my heart and they sent me to ER they monitored me on a EKG for a couple hours. I don't think they found anything and they sent me home. They did take XRAY of my chest and thought that i could have pneumonia but I didn't have any symptoms and they thought they say something so they started me on antibiotics that i took the next 5 days. I was feeling better on Monday. And I feel fine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- EKG-unknown Xray COVID-19 test- Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Cancer; Heart Bypass;
- Andere Medikamente
- Atorbastitain; Ruthatrin; Niosin ER; Vitamin D3; Magnesium; Turmeric; Fish Oil; Aspirin
- Allergien
- N/A
- Vorherige Impfungen
- Tired for 24-35 after most vaccines
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 02.04.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 44,0
- Dosis
- UNK
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Drainage
Headache
Lethargy
Pain
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Throat irritation
Symptomtext
May 16 started with scratchy throat. Progessed to congestion aches, fever, drainage, coughing, sneezing, lethargy. Later, after Paxlovid, headaches.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- took iHealth covid - 19 antigen rapid test. May 17 negative. May 19 positive. May 24 positive. May 26 negative test. May 28 negative test. Last test was a different at-home test I had on hand, but I don't remember the name.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- sulfa in meds
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 27.05.2022
- Impfdatum
- 18.03.2022
- Beginn
- 19.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Asthenia
Breast mass
Breast pain
Breast swelling
Contusion
Lymphadenopathy
Pain
Pyrexia
Skin warm
Symptomtext
On Saturday afternoon around 2pm had fever 102.0, body aches, felt arm and had "bruise", Right breast sore. By 7 PM felt weak. On Sunday-Lymph node is swollen and breast. Went to the ER on Monday and given Motrin 800mg only. On Tuesday-warm, hard lump on Right breast and swollen, seen by RN on Wednesday.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Breast pain
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 19.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 25,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Fatigue
Headache
Mucosal discolouration
Odynophagia
Oropharyngeal discomfort
Oropharyngeal pain
Pharyngeal erythema
Pyrexia
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Streptococcus test negative
Symptomtext
I was on an airplane on 4/24 and on 4/26 began having runny nose, congestion, headache, fever, cough, fatigue, and sore throat. The symptoms, specifically the sore throat progressed over the next few days. My throat was raw and felt like I was swallowing glass and had red and yellow spots in the back. I took a home Covid test on 4/27 and it was positive. On 4/29 I went and had a PCR test which was also positive. I was concerned about the possibility of a secondary infection so I went to a local urgent care clinic. They did a strep test which was negative but went ahead and prescribed some amoxycillin and prednisone. After starting the prescriptions, my symptoms began to improve and I felt better after a few days. And I finally tested negative with an at home Covid test after 10 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- At home Covid test positive. PCR Covid test positive. Strep test negative.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Gastritis; Osteoporosis; Osteopenia
- Andere Medikamente
- Calcium; vitamin D3; zinc; magnesium; omeprazole 20mg; melatonin
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 18.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 16.04.2022
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Dizziness
Electrocardiogram
Fatigue
Nasopharyngitis
Oropharyngeal pain
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
04/16/2022 I started to feel a sore throat in the evening. The next day I continued to have the sore throat and I was getting very fatigued throughout the day. Then I began to start to get runny noses, congestion about 4 days after. I tested positive the Friday after, about one week from feeling symptoms. I only had cold symptoms and fatigue for a few more days and then it started to go away. the following week, 2 weeks post initial symptoms, I only had fatigue as a continuing symptom. A new symptom came on being dizziness and it has lasted up until now As of now symptoms are all gone except for light amount of dizziness still continuing. My heart rate was also in the 40's during this time. I did have an EKG and also went in for dizziness. My heart rate is now in the 50s and I am going to be seeing a cardiologist again.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- EKG: showed 53 however from self testing on pulsometer I was in around 40s during covid infection.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Cholesterol and hypothyroidism
- Andere Medikamente
- Synthroid, Prilosec Generic Omeprazole, Atorvastatin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 16.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 07.05.2022
- Tage bis Beginn
- 22,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Cough
Discharge
Fatigue
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test
SARS-CoV-2 test positive
Seasonal allergy
Throat irritation
Vaccine breakthrough infection
Symptomtext
Breakthrough COVID on 05/09/2022. My case was very mild. It was mostly a scratchy and running nose, fatigue, coughing and a little bit of sore throat. I started taking the Paxlovid for 5 days. I feel fine, I have good energy. I just have a little drainage but I have allergies in the summertime anyways. I quarantine for 8 days. If I have to go out I use a mask.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Home test and a PCR test was the one that came back positive.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Hypothyroid; High Blood Pressure.
- Andere Medikamente
- Lisinopril 5mg; NP thyroid 120mg; progesterone cap 400mg; testosterone cream; Biest cream; berberine 1000mg; niacin 500mg; vitamin K2 45mcg; vitamin 5000 IU; multivitamin; vitamin C 300mg
- Allergien
- Morphine
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 14.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Confusional state
Vaccination site induration
Vaccination site pain
Vaccination site swelling
Symptomtext
Spacey; It is debilitating for her; Started noticing arm pain at the injection site/pain started getting worse; there is also hardness and some swelling associated with the pain, at the injection site; There is some swelling associated with the pain, at the injection site; This spontaneous case was reported by a consumer and describes the occurrence of CONFUSIONAL STATE (Spacey), ASTHENIA (It is debilitating for her), VACCINATION SITE PAIN (Started noticing arm pain at the injection site/pain started getting worse), VACCINATION SITE INDURATION (there is also hardness and some swelling associated with the pain, at the injection site) and VACCINATION SITE SWELLING (There is some swelling associated with the pain, at the injection site) in an 84-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. Co-suspect product included non-company product TRAMADOL for an unknown indication. It was reported that patient has never been diagnosed or tested positive for COVID-19. Previously administered products included for Product used for unknown indication: Pfizer (first dose), Pfizer (First booster) and Pfizer (second dose). Past adverse reactions to the above products included No adverse event with Pfizer, Pfizer and Pfizer. Concurrent medical conditions included Drug allergy (Benadryl). Concomitant products included IMMUNOGLOBULIN G HUMAN (IGG) for Booster, APIXABAN (ELIQUIS), METOPROLOL, FUROSEMIDE (LASIX [FUROSEMIDE]), PREGABALIN (LYRICA) and ACYCLOVIR [ACICLOVIR] for an unknown indication. On 04-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient started TRAMADOL (unknown route) at an unspecified dose. On 05-May-2022, the patient experienced CONFUSIONAL STATE (Spacey), VACCINATION SITE PAIN (Started noticing arm pain at the injection site/pain started getting worse), VACCINATION SITE INDURATION (there is also hardness and some swelling associated with the pain, at the injection site) and VACCINATION SITE SWELLING (There is some swelling associated with the pain, at the injection site). 05-May-2022, the patient experienced ASTHENIA (It is debilitating for her). At the time of the report, CONFUSIONAL STATE (Spacey), ASTHENIA (It is debilitating for her), VACCINATION SITE PAIN (Started noticing arm pain at the injection site/pain started getting worse), VACCINATION SITE INDURATION (there is also hardness and some swelling associated with the pain, at the injection site) and VACCINATION SITE SWELLING (There is some swelling associated with the pain, at the injection site) had not resolved. No other vaccines given within 1 month prior to Moderna COVID-19 vaccine. The patient received second booster shot on her right arm. The patient visited her HCP, who put her on Tramadol. After taking Taramadol, patient was spacey which the reporter thinks was from Tramadol and was not from Moderna. It was reported that except for the swelling, patient's symptoms had worsened since they first started, pain in right arm at injection site, hardness were worsened and swelling was stable. Reporter stated that it looks like the patient had something inflammatory going on. For swelling HCP prescribed Prednisone but patient had not started taking it yet.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy (Benadryl)
- Vorgeschichte
- Comments: It was reported that patient has never been diagnosed or tested positive for COVID-19.
- Andere Medikamente
- IGG; ELIQUIS; METOPROLOL; LASIX [FUROSEMIDE]; LYRICA; ACYCLOVIR [ACICLOVIR]; TRAMADOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 13.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site pain
Symptomtext
pain at the site of injection\received the Moderna vaccine on his left arm, which is where he was experiencing the pain; This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE PAIN (pain at the site of injection\received the Moderna vaccine on his left arm, which is where he was experiencing the pain) in an 85-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. No allergies (medications, food and other products) reported. Patient did not test COVID positive or diagnosed with it. No other vaccines given within 1 month prior to Moderna COVID-19 vaccine. Previously administered products included for Product used for unknown indication: Pfizer (Dose 1), Pfizer (1st booster) and Pfizer (Dose 2). Past adverse reactions to the above products included No adverse event with Pfizer, Pfizer and Pfizer. Concomitant products included PANTOPRAZOLE for GERD, APIXABAN (ELIQUIS), LOSARTAN, FINASTERIDE and FUROSEMIDE (LASIX [FUROSEMIDE]) for an unknown indication. On 04-May-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 05-May-2022, the patient experienced VACCINATION SITE PAIN (pain at the site of injection\received the Moderna vaccine on his left arm, which is where he was experiencing the pain). At the time of the report, VACCINATION SITE PAIN (pain at the site of injection\received the Moderna vaccine on his left arm, which is where he was experiencing the pain) was resolving. On the morning of 05-MAY-2022, He received the Moderna vaccine on his left arm, which was where he was experiencing the pain. He said that the pain was still somewhat there, but it never inhibited him from doing any activities. He said that the pain was improving since it first started. Outcome was very slight residual effects. Adverse event did not cause patient to seek medical care. No treatment drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: No allergies (medications, food and other products) reported. Patient did not test COVID positive or diagnosed with it. No other vaccines given within 1 month prior to Moderna COVID-19 vaccine.
- Andere Medikamente
- ELIQUIS; LOSARTAN; FINASTERIDE; LASIX [FUROSEMIDE]; PANTOPRAZOLE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 11.05.2022
- Impfdatum
- 05.04.2022
- Beginn
- 08.05.2022
- Tage bis Beginn
- 33,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dizziness
Exposure to SARS-CoV-2
Feeling abnormal
Headache
Malaise
Nausea
Pain
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Symptomtext
I started feeling mild symptoms on Friday, I contacted my doctor because I had been exposed to COVID. I went in for a PCR test. On Saturday, I felt much worse. I had headaches, body aches, runny nose, sneezing. It felt like the worse cold you could ever have. On Sunday, the test came back positive. I was prescribed Paxlovid which has helped. On Tuesday, I started experiencing dizziness and nausea. I have been prescribed Meclizine to help me with both the nausea and dizziness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- In remission for Leukemia
- Andere Medikamente
- Flomax
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 09.03.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 57,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Aggression
COVID-19
Confusional state
Cough
Electrocardiogram abnormal
Mental status changes
Pyrexia
Refusal of treatment by patient
Sinus rhythm
Vaccine breakthrough infection
Symptomtext
COVID-19 BREAKTHROUGH: The patient presents with cough, fever, change in regular mentation. 84 y/o F with a PMHx of Alzheimer's disease and dementia presents to the ED brought in by her granddaughter with daughter at bedside c/o cough, fever, and change in regular mentation with an onset PTA. Pt hx is limited due to clinical condition. Pt's granddaughter states that the pt has been acting more confused than usual. In the room pt is combative and refusing to let nursing staff and provider touch her. The course/duration of symptoms is unknown. The degree at onset was un
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- SINUS ABNORMAL RHYTHM ECG.
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- ALZ, DEMENTIA,
- Andere Medikamente
- UNKNOWN
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 06.05.2022
- Impfdatum
- 09.03.2022
- Beginn
- 05.05.2022
- Tage bis Beginn
- 57,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Aggression
COVID-19
Confusional state
Cough
Electrocardiogram abnormal
Mental status changes
Pyrexia
Refusal of treatment by patient
Sinus rhythm
Vaccine breakthrough infection
Symptomtext
COVID-19 BREAKTHROUGH: The patient presents with cough, fever, change in regular mentation. 84 y/o F with a PMHx of Alzheimer's disease and dementia presents to the ED brought in by her granddaughter with daughter at bedside c/o cough, fever, and change in regular mentation with an onset PTA. Pt hx is limited due to clinical condition. Pt's granddaughter states that the pt has been acting more confused than usual. In the room pt is combative and refusing to let nursing staff and provider touch her. The course/duration of symptoms is unknown. The degree at onset was un
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- SINUS ABNORMAL RHYTHM ECG.
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- ALZ, DEMENTIA,
- Andere Medikamente
- UNKNOWN
- Allergien
- PENICILLIN
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Decreased appetite
Exposure during pregnancy
Fatigue
Hypersomnia
Impaired work ability
Live birth
Nausea
Symptomtext
I was 18 weeks pregnant at the time of my booster shot on 3/25/22. I had some nausea in the first trimester but had been feeling better and more energetic by mid-March. This was my 3rd shot but I had also had COVID in Dec of 2020. At the time of having COVID, I gave birth at 38 weeks to a healthy baby boy. I had some tiredness after the first two shots in August and September of 2021. My OB, Dr, wanted me to get the booster as soon as I could, which would have been 3/24/22. I got the 3rd Moderna shot on 3/25/22. Within 10 minutes of getting the shot, I because extremely nauseous. The whole weekend, I slept and couldn?t eat anything because of the nausea and extreme tiredness. I thought it would go away but the nausea got worse that week and has remained bad enough to need a prescription for Zofran that I use at least once a day. I am still extremely tired, which I wasn?t early in my pregnancy and have had to miss several days of work because of these symptoms. It?s worse than when I had COVID and lasting longer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Chronic Migraine, Interstitial Cystitis, Premature Ventricular Contractions
- Andere Medikamente
- Zyrtec, Lexapro, prenatal vitamin, folic acid
- Allergien
- Strawberries, zomig, azithromiacin, surgical steel
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 03.05.2022
- Impfdatum
- 18.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 8,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
COVID-19
Feeling abnormal
Headache
Malaise
Paranasal sinus hypersecretion
Rhinorrhoea
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
On 04/26/2022 I has a very runny nose in the evening. My husband had symptoms on 04/20/2022 and took a home-test and that was positive on Wednesday morning 04/23/2022 and my at-home, Rapid, and PCR test was Negative. I took an at-home test on 04/25/2022 that was also Negative. I did take another at-home test on 04/27/2022 and that was Positive so I went to Urgent Care where a rapid test confirmed Positive. I was prescribed a Z-PAK and Steroids at that visit on 4/23/2022 because I had symptoms. After 04/27/2022 I had a slight headache and felt fuzzy-headed and that only lasted a half day and went away. I always have sinus drainage so I already had those symptoms around this time of year. As far of COVID-19 I had no other symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 04/23/2022 At-Home, Rapid, and PCR test NEG; 04/25/2022 At-Home test NEG; 04/27/2022 At-Home and Rapid test Positive.
- Aktuelle Erkrankungen
- Seasonal allergies
- Vorgeschichte
- Hypertrophic Cardiomyopathy (HCM); High Cholesterol; High Blood pressure
- Andere Medikamente
- Metoprolol 25mg once daily, Oxybutynin, Amlodipine, Atorvastatin, Hydrochlorothiazide 12mg Once daily, Vitamin D, Multivitamin, B12, Vitamin C, Metamucil, Generic Claritin, and Elderberry.
- Allergien
- Penicillin; Ceclor; Azithromycin; Sulfa
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 10.02.2021
- Beginn
- 11.03.2021
- Tage bis Beginn
- 29,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Abdominal distension
Abdominal pain
Colitis ulcerative
Colonoscopy abnormal
Diarrhoea
Flatulence
Symptomtext
Started having abdominal pains, bloating, gas, diarrhea
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- 4/18/2022 colonoscopy diagnosis ulcerative colitis
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension and GERD
- Andere Medikamente
- Lisinopril/ Htcz 20/25 mg daily
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 01.05.2022
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site pain
Injection site swelling
Symptomtext
Site: Pain at Injection Site-Mild, Site: Swelling at Injection Site-Mild
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 23.04.2022
- Beginn
- 23.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Influenza like illness
Injection site pain
Oedema peripheral
Pain
Tenderness
Symptomtext
Received #3 Moderna boost on Saturday 4/23/22 to left deltoid with no immediate abnormal s/e to arm. Next day patient reported slight flu-like symptoms. On 4/26/22 patient arrived at Walk In Clinic reporting radiating 4/10 pain level in left top shoulder, associated deltoid, and left underarm pit with swelling and tenderness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Type 2 Diabetes
- Andere Medikamente
- Metformin 500mg tablet daily
- Allergien
- Sulfa, Trimethoprim.
- Vorherige Impfungen
- Only slight flu-like symptoms after 2nd Covid-19 Moderna vaccine.
- Staat
- NC
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 25.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Hypersomnia
Oral herpes
Oral mucosal blistering
Oropharyngeal blistering
Pyrexia
Tongue blistering
Symptomtext
Patient stated since she received the second booster 04/13/2022, she has experienced the following: * Sleeping almost the entire next day after the vaccine * Having a mild fever for at least 2-3 days post vaccination. * Fever blisters that appeared all of a sudden a few days post vaccination around her mouth. The Fever blisters have increased over the past week, insude her mouth, down her tongue and throat as noted by her pcp. Patient saw her pcp 04/25/2022 and was prescribed a mouth wash to help with blisters. Here pcp instructed her to notify the health department where she received her booster. Patient reported she "passed out " with her first booster in Nov 2021 and resulted with a broken ankle. Patient received first booster at a pharmacy, not the health department.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Patient went to her pcp for evaluation 04/25/2022.
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- Patient stated received a prescription mouthwash 04/25/2022 to start using for her mouth blisters and throat blisters. Patient saw her pcp 04/25/2022and pcp stated patient should report adverse reaction to the local health department.
- Allergien
- na
- Vorherige Impfungen
- Moderna COVID19 vaccine. First booster was 11/2021 and she "passed out". She got the vaccine at a local pharmacy.
- Staat
- CT
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 23.04.2022
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash macular
Rash pruritic
Symptomtext
About 4.5 hours after receiving her 4th dose of Moderna (second booster), she noticed a rash and blotchy red spots on her hands, arms, mid-section, and upper legs. They were not raised, but were itchy. She applied Ivarest cream (which has an antihistamine in it) and took a cool bath with Aveeno, and reported some relief of the itching. Today (the day after), she called me to report the adverse event. She reports today that the rash is already starting to improve and lighten, though the itchiness has not improved. I took the information and suggested she take an oral antihistamine. She had Zyrtec on hand, so that's what she took. She saw her PCP a couple hours later, and he recommended the exact same thing. The prescriber concluded that she should not get another booster within the next 6 months (if another becomes recommended), and that if she does ever get another covid shot, she should choose a different one.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 23.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash pruritic
Symptomtext
Overnight within 36 hours of receiving the Moderna booster I developed a full body painful and itchy red rash. It was mainly on the trunk of my body, front and back, spreading to my inner thighs, and up the side of my neck on the right side, where the injection was given. The rash is continuing nearly 72 hours after the injection. Treating with Benadryl 25 mg every 4 hours and applying topical Diphenhydramine HCL & Zinc Acetate. Today the rash is subsiding. I have not needed to use the Epipen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hyperlipidemia, seasonal allergies and sinusitis, osteopenia.
- Andere Medikamente
- Lipitor 20 mg, Divigel 0.25 mcg, Flonase 0.50 mcg nasal spray, Benadryl 25 mg, Calcium 1200 mg plus Vitamins D & K supplement.
- Allergien
- IV Contrast Dye, Thimerosal, artificial colors added to food. Suspected allergies to PEG (Covid vaccine and Tylenol) and Adjuvanted vaccines (FLUAD).
- Vorherige Impfungen
- FLUAD vaccine 9/2020; Pfizer Covid vaccine 3/22/21; Janssen Covid vaccine 11/10/21
- Staat
- SC
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 18.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 5,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Pruritus
Throat tightness
Urticaria
Symptomtext
12 days after the booster I developed dermatographia. My throat started to close up and my entire body itched and broke out into hives. Benadryl wouldn't bring much relieve other than for an hour or 2 and then consulted a dermatologist. After the first round of low dose steroids it didn't help that much and have now been prescribed more, which I will start tomorrow.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 15.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Rash macular
Skin exfoliation
Symptomtext
looks like burn blotches under his right vaccinated arm, below elbow. he rubbed one and the skin fell off.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash macular
- Hospital-Tage
- -
- Labordaten
- Went to see md after we talked and md thinks it caused a shingles breakout.
- Aktuelle Erkrankungen
- glossitus- pt thinks from previos pfizer shot, which md was treating.
- Vorgeschichte
- -
- Andere Medikamente
- cialis, duloxetine, omeprazole, lidocaine, tamsulosin, diazepam, azithromycin, escitalopram, nystatin, and rosuvastatin.
- Allergien
- nkda
- Vorherige Impfungen
- glossitus from pfizer
- Staat
- WV
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 24.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Asthenia
Hypoaesthesia
Injection site erythema
Injection site oedema
Local reaction
Muscular weakness
Pain in extremity
Spinal X-ray
Symptomtext
Localized reaction to injection - Has not resolved - Edema and erythema present. Bilateral arm numbness and upper extremity weakness starting on 3/25/ 2022 at 3am. Symptoms ongoing - bilateral arm pain and weakness at night intermittently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- XR Cervical Spine AP/Lateral 4/14/2022
- Aktuelle Erkrankungen
- Contact Dermatitis - 3/10/2022 - Resolved
- Vorgeschichte
- Asthma
- Andere Medikamente
- Symbicort 80-4.5 mcg/actuation inhaler bid. Duo-Neb Nebulizer Q6hrs PRN.
- Allergien
- No know allergies.
- Vorherige Impfungen
- Moderna COVID-12 (lot 013L20A) Adverse event: Similar numbness but short lasting for a few days - resolved. Patient was 35 at
- Staat
- IN
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Symptomtext
Pt states that her RIGHT elbow started hurting the day after the vaccine and within the last few days her RIGHT shoulder is hurting her. Her vaccine was given in the left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- none stated by pt
- Vorgeschichte
- none stated by pt
- Andere Medikamente
- unknown
- Allergien
- "meperidine and related"
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 06.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site erythema
Vaccination site rash
Vaccination site swelling
Vaccination site warmth
Symptomtext
PATIENT STOPPED BY THE PHARMACY AT 3:56PM TO SHOW ME THE ODD SHAPED FOUR PLUS INCH RED RAISED WARM RASH OVER THE VACCINATION SITE. I ADVISED SHE SHOW IT TO HER DOCTOR OR POSSIBLY TRY AN ANTIHISTAMINE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site rash
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- ASTHMA, HTN
- Andere Medikamente
- UNKNOWN
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site nodule
Vaccination site pain
Vaccination site swelling
Vaccination site warmth
Symptomtext
PATIENT CALLED TODAY AT 3:45 PM CONCERNED THAT THE VACCINATION SITE HAD DEVOPED A PAINFUL KNOTT, APPORIMATELY A QUARTER IN SIZE AREA OF SWELLING AND SOME HEAT. I RECOMENED THAT SHE HAVE IT SEEN BY A DOCTOR
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site pain
- Hospital-Tage
- -
- Labordaten
- UNKNOWN
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- ASTHMA
- Andere Medikamente
- UNKNOWN
- Allergien
- MACROLIDES, PENICILLINS, SULFAS
- Vorherige Impfungen
- "A SHOT MADE ME SICK & FELL OVER"
- Staat
- MA
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Fatigue
Injection site pain
Injection site swelling
Lethargy
Pain
Pyrexia
Symptomtext
Site: Pain at Injection Site-Medium, Site: Swelling at Injection Site-Medium, Systemic: Abdominal Pain-Mild, Systemic: Body Aches Generalized-Medium, Systemic: Exhaustion / Lethargy-Mild, Systemic: Fever-Mild, Additional Details: symptoms are ongoing
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 06.04.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site swelling
Symptomtext
Softball size swelling at injection site lasting 3-4 days. Treated at home with ice/ cold compresses
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- GERD neurocardiogenic syncope Pancreatitis Anxiety
- Andere Medikamente
- none
- Allergien
- latex flu vaccine
- Vorherige Impfungen
- Anaphylaxis to flu vaccine in 2010
- Staat
- AZ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site haematoma
Injection site pain
Injection site pruritus
Injection site reaction
Injection site swelling
Skin hypertrophy
Symptomtext
Patient has pain , swollen, itching , thickness on site, redness and heat. Day after getting vaccine redness has been spread from 3.5 ins to 4.5 ins on the 5th day and still has heat and itching on site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- IBUPROFEN 200 MG
- Allergien
- NO KNOWN ALLERGIES TO MEDICATION
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 30.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Headache
Nausea
Pyrexia
Symptomtext
Chills , fever 99.3 ( my norm 96.3-.7) , tired, slight nausea, headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Type I diabetes, hypertension, hashimotos disease
- Andere Medikamente
- -
- Allergien
- Penicillin
- Vorherige Impfungen
- Shingles 2021
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 28.03.2022
- Impfdatum
- 25.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Injection site erythema
Injection site pain
Injection site pruritus
Injection site swelling
Symptomtext
REPORT REDNESS, PAIN SWELLING, ITCHINESS AT THE SITE OF INJECTION AND JOINT PAIN
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HYPOTHYROID,ARTHRITIS,BURSITIS,HTN
- Andere Medikamente
- LEVOTHROID,AMOLDIPINE,THDROCHORTHIAZIDE,MOTRIN
- Allergien
- VICODIN
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Facial discomfort
Lip swelling
Lymphadenopathy
Rash
Vaccination site erythema
Vaccination site pain
Symptomtext
face was tight; lips are swollen; Rashes that looks like bug bites around her mustache area and her jaw lines (on both side)/The rashes are white circle with red edges.; Injection site red/Injection site had a 6 inches red ring around it; Armpit was swollen (like the size of a golf ball); Injection site tender; Injection site sore; This spontaneous case was reported by a consumer and describes the occurrence of FACIAL DISCOMFORT (face was tight), LIP SWELLING (lips are swollen), VACCINATION SITE PAIN (Injection site tender), VACCINATION SITE PAIN (Injection site sore) and RASH (Rashes that looks like bug bites around her mustache area and her jaw lines (on both side)/The rashes are white circle with red edges.) in a 29-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 046L21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. No Medical History information was reported. On 11-Mar-2022, the patient received first dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 18-Mar-2022, the patient experienced VACCINATION SITE PAIN (Injection site tender), VACCINATION SITE PAIN (Injection site sore), VACCINATION SITE ERYTHEMA (Injection site red/Injection site had a 6 inches red ring around it) and LYMPHADENOPATHY (Armpit was swollen (like the size of a golf ball)). On 22-Mar-2022, the patient experienced FACIAL DISCOMFORT (face was tight), LIP SWELLING (lips are swollen) and RASH (Rashes that looks like bug bites around her mustache area and her jaw lines (on both side)/The rashes are white circle with red edges.). On 21-Mar-2022, VACCINATION SITE PAIN (Injection site tender), VACCINATION SITE PAIN (Injection site sore) and VACCINATION SITE ERYTHEMA (Injection site red/Injection site had a 6 inches red ring around it) had resolved. At the time of the report, FACIAL DISCOMFORT (face was tight), LIP SWELLING (lips are swollen) and RASH (Rashes that looks like bug bites around her mustache area and her jaw lines (on both side)/The rashes are white circle with red edges.) had not resolved and LYMPHADENOPATHY (Armpit was swollen (like the size of a golf ball)) was resolving. The action taken with mRNA-1273 (Spikevax) (Intramuscular) was unknown. Based on what she looked up online, the injection site reaction can be described as the COVID arm. The injection site reaction went away by itself yesterday morning and the swollen part of her armpit has reduced to half of the size it was when the reaction stared. There has been no changes to her diet or soap. Concomitant medications details were not reported by the reporter. Treatment details was not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- HI
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 20.02.2022
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Headache
Symptomtext
Complains of Headaches consistantly after a shot. 1 week after use Suggested going to a primary MD for follow up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- OC
- Allergien
- No Known
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 16.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Oxygen saturation decreased
Pain
Parotitis
Swelling face
Swollen tongue
Symptomtext
3/18/2022 oxygen saturation dropped and supplement oxygen needed. 3/19/2022 patient c/o pain with swollen left side of face and tongue. Transferred to hospital. Hospital gave diagnosis of parotitis. Patient still in hospital at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- fracture of lower end of left femur, acute posthemorrhagic anemia
- Vorgeschichte
- chronic kidney disease, iron deficiency anemia, retention of urine, COPD, chronic bronchitis, neuromuscular dysfunction of bladder, GERD, depression, muscle weakness r/t cerebral infarction, pure hypercholesterolemia, dysphagia
- Andere Medikamente
- amlodipine, atorvastatin, miralax, multivitamin-minerals, senna-docusate, aspirin, hydralazine, hypromellose solution, lexapro, metoprolol, omeprazole, sodium bicarbonate, acetaminophen, calcitrate, clonazepam, methocarbamol, senna, tramado
- Allergien
- buPROPion, Augmentin
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 19.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Axillary pain
Extra dose administered
Injection site mass
Injection site pain
Injection site pruritus
Injection site rash
Lymphadenopathy
Pyrexia
Symptomtext
I received a baseball size lump at injection site the next morning. It was painful. After a few days it went down and the rash spread all the way down my arm to my elbow. I had high fever first 24 hours of 101 and then low grade even today. The itch and pain has no travelled to my armpit and elbow. My lymph are also swollen in my armpit and chest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Just using over the counter medications: Benadryl, ice compress, Claritin, cortisone cream, Tylenol
- Aktuelle Erkrankungen
- None known.
- Vorgeschichte
- Atrial fibrillation, rheumatic fever, acid reflux
- Andere Medikamente
- Metoprolol, flecanide, valtrex, Hydrochlorothiazide, omeprazole, eliquis, hydroxyzine
- Allergien
- Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site swelling
Pruritus
Symptomtext
Severe itching that lasted a few days along with inject site swelling. Events started 2 hours after the injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 14.03.2022
- Impfdatum
- 03.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Symptomtext
Rash on entire face.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Na
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High BP
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 13.03.2022
- Impfdatum
- 12.03.2022
- Beginn
- 12.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Dizziness
Fatigue
Flushing
Hyperhidrosis
Lethargy
Nausea
Vomiting
Symptomtext
Systemic: Chills-Medium, Systemic: Dizziness / Lightheadness-Severe, Systemic: Exhaustion / Lethargy-Severe, Systemic: Flushed / Sweating-Severe, Systemic: Nausea-Severe, Systemic: Vomiting-Severe, Additional Details: Patient experience emesis within 15 minutes of injection. Other sypmtoms were also felt at this time. Appeared to recover after receiving water.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site bruising
Symptomtext
Site: Bruising at Injection Site-Medium
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 07.03.2022
- Impfdatum
- 05.03.2022
- Beginn
- 06.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hyperaesthesia
Injection site erythema
Injection site mass
Injection site pain
Injection site reaction
Injection site swelling
Injection site warmth
Musculoskeletal stiffness
Symptomtext
Left Arm now has a large, very red, swollen painful lump, arm is stiff, sore & painful to even have clothes touching injection site. Can feel the heat at the injection site thru my shirt.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High cholesterol, high blood pressure
- Andere Medikamente
- Rosuvastatin 20mg Metoprolol 100mg
- Allergien
- Shellfish/iodine
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- -
- Geschlecht
- F
- Eingang
- 05.03.2022
- Impfdatum
- 13.05.1970
- Beginn
- 05.03.2022
- Tage bis Beginn
- 18.924,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Rash
Symptomtext
Staff member stated that the patient drove there for treatment that a rash that developed, but was not sure if it was from her anxiety or the vaccine itself. They administered decadron and diphenhydramine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Unknown
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 04.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Adverse reaction
Dizziness
Pallor
Symptomtext
Pt. Was a 54 Y/O M, A+OX4 that experienced an adverse reaction after being vaccinated. After vaccination, patient became pale and experienced dizziness at the sight of his own blood. Pt. Has a history of a fear of blood but disclosed this information after being vaccinated. Patient did not lose consciousness nor experience any fall. Pt. Was placed in supine position with head supported by nurses and given a snack with water. Vaccination clinician was LVN and Medical Oversight clinician was NP . Pt. V/S were HR:62 B/P:115/73 02 Sat:97% at 1327. Patient was kept in observation area for 30 minutes. Pt. Remained stable and was alert and oriented with no further occurrences. Pt. Verbalized feeling well before leaving clinic. Pt. Was accompanied by his spouse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
C-reactive protein
Fatigue
Full blood count
Impaired work ability
Metabolic function test
Pain
Symptomtext
Onset of extreme body aches,overwhelming fatigue onset 2/24/22 @ 1900 which have continued > 1 week after vaccine causing inability to work
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- CBC, CMP, C Reactive protein 3/3/22.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hyper cholesterol
- Andere Medikamente
- Aspirin, multivitamin, melatonin
- Allergien
- IVP DYE
- Vorherige Impfungen
- Extreme body aches, fatigue, Fever, feeling of impending doom after Pfizer 2nd dose 1/7/21. 58 years old at time. Symptoms resol
- Staat
- SD
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 03.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Painful respiration
Pyrexia
Symptomtext
Symptoms reported were headache, chills, fever with a temperature of 102 degrees, and lungs hurt when taking a deep breathe. Lasted for 24 hrs and then gone the next day. Was not assessed and evaluated by a medical provider and returned to work.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- none done in a medical facility.
- Aktuelle Erkrankungen
- patient report on screening questionnaire - no
- Vorgeschichte
- Attention Deficit Hyperactivity Disorder,
- Andere Medikamente
- unknown
- Allergien
- amoxicillin, popcorn, and sulfamethoxazole/trimethoprim
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 25.02.2022
- Beginn
- 27.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pain
Swelling
Tenderness
Symptomtext
Received tdap 0945am 02/25/2022 then received moderna booster at 630pm 02/25/2022. Reports swelling, redness, and pain to 20yo BCG vaccine scar beginning Sunday 02/27/2022. Redness has improved but tenderness to touch, swelling is the same.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 21.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Neck pain
Pain
Pain in extremity
Symptomtext
Patient stated that he woke up on 2-23-22 and adjusted his pillow with his left arm and began having shooting pain that radiated up and down his left arm and neck. He said that one day later his arm became numb and he rubbed it with green alcohol. He stated that his arm is no longer numb, but stings when he moves it up and down, but doesn't hurt at rest. He has not gone for medical attention at this time. He said he is going to wait to see if pain improves.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- Patient hasn't had any lab or other medical tests at this time
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension, hypercholesterolemia, anxiety, neuropathy, chronic back pain from previous surgeries (rods and screws placed), right arm pain.
- Andere Medikamente
- Hydrochlorothiazide, gabapentin, anxiety medication , 2 blood pressure medications, cholesterol medication, and occasional aleve otc,
- Allergien
- aspirin allergy
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 24.02.2022
- Impfdatum
- 22.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Pyrexia
Symptomtext
Patient received the 0.5 ml Moderna covide vaccine for the booster when it should be 0.25ml. Patient was called by provider to inform the event and patient stated mild fever on 2/23 and feel fine today on 2/24 denies any more fever.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 19.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Injection site warmth
Pyrexia
Symptomtext
Patient called 02/24 reporting injection site is warm and red and swollen, she stated that is feverish. I recommended that she reach out to her primary care doctor or go to the local urgent care as it could be an infection or immune reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- na
- Vorgeschichte
- na
- Andere Medikamente
- N/A
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 24.02.2022
- Impfdatum
- 22.02.2022
- Beginn
- 22.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Urticaria
Symptomtext
Moderna booster of 0.25 mL that resulted in this visit. Pt previously required observational stay after 2nd dose of Pfizer COVID-19 vaccine in June 2021. Now pt is admitted after reaction to Moderna COVID-19 booster dose. Pt woke up following morning with hives. Pt was given epinephrine, benadryl, and dexamethasone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hx of DRESS with cephalexin
- Andere Medikamente
- -
- Allergien
- Pfizer COVID-19 vaccine, cephalosporins, penicillins, IV contract dye, gluten, sulfadiazine, phenytoin
- Vorherige Impfungen
- Pfizer vaccine, June 2021, pt experienced rash
- Staat
- TN
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 16.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Chest discomfort
Cough
Malaise
Pyrexia
Symptomtext
Fever, chest pressure, general malaise cough, feeling of impending doom lasting 14 hours
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Triamterene/HCTZ 37.5-25
- Allergien
- Sulfa, Lisinopril
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Cardiac flutter
Confusional state
Fatigue
Feeling cold
Hyperhidrosis
Laboratory test
Pain
Vaccination complication
Symptomtext
fluttering of under heart on left side, extreme confusion, tiredness, aches and pains. freezing but heavy sweating. started the night <Monday night/Tuesday morning, of the dose given. feeling of tiredness and confusion still happening on 2/22/2022 but to a lesser degree. On Feb 17, 2022 went to emergency room where diagnosed with allergic reaction to vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Feb 17, 2022 labs where ran on blood and tests done on heart.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetic, hypertension (high cholesterol), chronic knee and back pain
- Andere Medikamente
- icosapent ethyl, Lantus, metformin, jardiance, hydrochlorothiazide, atorvastin, fenofibrate, Vit D, tramadol, tylenol, multi vitamin.
- Allergien
- dust, cats
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 18.02.2022
- Beginn
- 18.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenopia
Disturbance in attention
Dizziness
Hyperhidrosis
Lethargy
Malaise
Symptomtext
Patient came back to pharmacy within 5 minutes of receiving her vaccine and stated she did not feel well. She was lightheaded, dizzy, profusely sweating, and lethargic. She never completely lost consciousness but had difficulty concentrating and keeping her eyes open.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 13.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Rash erythematous
Rash macular
Rash papular
Skin warm
Symptomtext
COVID arm, red raised hop spot, rash on both arms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 09.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest discomfort
Eye disorder
Eye irritation
Feeling abnormal
Interchange of vaccine products
Nausea
Oropharyngeal pain
Pain in jaw
Symptomtext
Moderna vaccine booster given at 2:02 PM with subsequent symptoms of eyes burning, strained, and ?not feeling right.? Medical provider called to assess at 1417. ROS otherwise negative. Vital signs done at 1417 which included a blood pressure 134/82, oxygen saturation 95% on room air, pulse 71. He seemed concerned and attributed all of this to the vaccine noting that after the first 2 vaccines he has had to have extensive GI work-up including a HIDA scan and a camera pill and multiple ER visits. His doctor initially told him not to get the vaccine but then cleared him for this booster dose. His current symptoms include that he feels that his "eyes are not right? and ?feels off.? No rash, itching, trouble breathing, chest pain, headache 1435 another set of vitals were done with an oxygen saturation of 97%, pulse 72, blood pressure 146/95. His sclerae white, pupils equal and extraocular movements are intact. There is no facial asymmetry. He denies blurry vision. Oropharynx is clear. He is moving his arms and legs symmetrically. His speech is clear. Mentation is clear. Heart is regular in rate and rhythm, lungs are clear to auscultation with unlabored respirations. He reports that his oxygen normally runs normal. At 1448 his oxygen saturation was 95% and he feels drawn out, "does not feel right" and is developed a pain in his R jaw which a few minutes later he noted moved down into his throat. He has no drooling or trouble swallowing and denies flatly any shortness of breath or wheezing. Lungs clear with good aeration. Oxygen 2 L nasal cannula was applied. At 1453 he reports discomfort in his upper chest extending from his jaw, skin is warm and dry, heart is regular in rate and rhythm respirations are unlabored. No scratching of his throat difficulty swallowing or drooling. Exam unremarkable. Shortly thereafter began to complain of nausea ?I never throw up.? 1454 oxygen saturation 98% on 2 L pulse 71. EMS arrived shortly thereafter ? report given, and they assumed care. To transport to hospital. Patient was able to stand up and walk to the stretcher. His skin was warm and dry.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- GI SYMPTOMS X1 YEAR
- Andere Medikamente
- BLOOD PRESSURE MEDICATION, ADVAIR, ZOFRAN, LEVSIN, VIT D, ALBUTEROL
- Allergien
- NKA
- Vorherige Impfungen
- REPORTS CONTINUOUS GI UPSET SINCE RECEIVING PRIMARY VACCINE SERIES WITH PFIZER 1 YEAR AGO, REPORTS HIS MEDICAL PROVIDER DIRECTED
- Staat
- NY
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 09.10.2021
- Impfdatum
- 04.09.2021
- Beginn
- 04.09.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Headache
Neck pain
Symptomtext
Started with head and neck pain. Extended to allover joint pain. Most significant in knees and ankles.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Blood pressure medication
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 27.10.2023
- Impfdatum
- 23.06.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine adminstered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 27.10.2023
- Impfdatum
- 28.06.2022
- Beginn
- 28.06.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine adminstered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 27.10.2023
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine adminstered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 27.10.2023
- Impfdatum
- 22.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine adminstered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 27.10.2023
- 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: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 27.10.2023
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 27.10.2023
- Impfdatum
- 12.04.2022
- Beginn
- 12.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 27.10.2023
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 27.10.2023
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 27.10.2023
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 27.10.2023
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 26.10.2023
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 26.10.2023
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 26.10.2023
- Impfdatum
- 26.04.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 26.10.2023
- 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: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 26.10.2023
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 26.10.2023
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 26.10.2023
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 26.10.2023
- 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: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 26.10.2023
- Impfdatum
- 21.04.2022
- Beginn
- 21.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 26.10.2023
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 26.10.2023
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine administered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 26.10.2023
- Impfdatum
- 28.04.2022
- Beginn
- 28.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
Vaccine adminstered after BUD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 07.08.2023
- Impfdatum
- 20.02.2022
- Beginn
- 09.11.2022
- Tage bis Beginn
- 262,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Transient ischaemic attack
Symptomtext
TRANSIENT CEREBRAL ISCHEMIA
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Transient ischaemic attack
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 04.08.2023
- Impfdatum
- 02.03.2022
- Beginn
- 14.03.2023
- Tage bis Beginn
- 377,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Neuropathy peripheral
Symptom recurrence
Symptomtext
NEUROPATHY 3/12/2023 -- RECURRENCE OF HOSPITALIZATION WITH SAME SYMPTOMS
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neuropathy peripheral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 04.08.2023
- Impfdatum
- 01.04.2022
- Beginn
- 08.03.2023
- Tage bis Beginn
- 341,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Neuropathy peripheral
Obstructive sleep apnoea syndrome
Symptomtext
OBSTRUCTIVE SLEEP APNEA PERIPHERAL NEUROPATHY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neuropathy peripheral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 25.07.2023
- Impfdatum
- 20.02.2022
- Beginn
- 06.01.2023
- Tage bis Beginn
- 320,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough case admission after 3 vaccines Moderna 3/9/21 lot# 010A21A; Moderna 4/6/21 lot# 025B21A; Moderna 2/20/22 lot# 046L21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 24.05.2023
- Impfdatum
- 11.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Patient was given .5ml of Moderna vaccine instead of .25ml for 2nd covid booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- acetaminophen ciclopirox shampoo ClearLax fexofenadine multivitamin PreviDent Booster Plus dental paste Vitamin D3 zinc
- Allergien
- Zyrtec
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 23.05.2023
- Impfdatum
- 07.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Patient was given .5ml instead of .25ml of Moderna vaccine for 2nd covid booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- ClearLax cyclobenzaprine dutasteride Fluzone High-Dose Quad Gentile Laxative (bisacodyl) levothyroxine sildenafil tretinoin topical cream
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 23.05.2023
- Impfdatum
- 12.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
Patient was given .5ml of Moderna vaccine instead on .25ml for 2nd covid booster. No adverse reaction reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CHF, h/o of prostate cancer
- Andere Medikamente
- amoxicillin Aspirin carvedilol clonazepam doxycycline monohydrate escitalopram ferrous sulfate fluticasone propionate/actuation nasal spray furosemide Miralax multivitamin primidone ramipril simvastatin Vitamin D3
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 23.05.2023
- Impfdatum
- 12.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
Patient was given .5ml of Moderna vaccine instead of .25ml, for 2nd covid booster. No adverse reactions reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Aleve aspirin diclofenac Fe-Tabs (iron) fluorouracil metronidazole minocycline Osteo Bi-Flex simvastatin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 24.04.2023
- Impfdatum
- 22.04.2022
- Beginn
- 16.08.2022
- Tage bis Beginn
- 116,0
- Dosis
- 4
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Feeling abnormal
No adverse event
Respiratory tract congestion
Rhinorrhoea
Symptomtext
I did not have an adverse reaction to the vaccine. I tested positive for COVID-19 on 08/16/2022. I had a runny nose, congested and just felt bad. I contacted my doctor, and I got a prescription Paxlovid. I tolerated the medication without any complications. As of today, I do not have any lingering symptoms of COVID-19.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- 16AUG2022 COVID-19 Test - Positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 97,0
- Geschlecht
- F
- Eingang
- 13.04.2023
- Impfdatum
- 09.02.2022
- Beginn
- 14.05.2022
- Tage bis Beginn
- 94,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute kidney injury
Computerised tomogram thorax abnormal
Hypersensitivity
Hypoxia
Mental status changes
Symptomtext
HYPOXEMIA 5/14/2022 ALTERED MENTAL STATUS, UNSPECIFIED ALLERGIC REACTION, INIT 5/14/2022 ALTERED MENTAL STATUS, UNSPECIFIED ALLERGIC REACTION, SUBSEQ 5/14/2022 ALTERED MENTAL STATUS, UNSPECIFIED HYPOXEMIA 5/14/2022 ABNL CHEST CT SCAN ALLERGIC REACTION, INIT 5/14/2022 ABNL CHEST CT SCAN ALLERGIC REACTION, SUBSEQ 5/14/2022 ABNL CHEST CT SCAN HYPOXEMIA 5/14/2022 NONTRAUMATIC ACUTE KIDNEY INJURY ALLERGIC REACTION, INIT 5/14/2022 NONTRAUMATIC ACUTE KIDNEY INJURY ALLERGIC REACTION, SUBSEQ 5/14/2022 NONTRAUMATIC ACUTE KIDNEY INJURY
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute kidney injury
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- F
- Eingang
- 15.03.2023
- Impfdatum
- 17.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 12,0
- Dosis
- 5
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Laboratory test normal
Rosacea
Skin disorder
Skin warm
Symptomtext
I had a lot of skin issues, my cheeks were very red, and hot to the touch. I went to the Dermatologist, and I was diagnosed with Rosacea. I was prescribed Oxymetazoline HCL/Ivermectin/Niacinamide. It is improving but I am still dealing with this currently.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- JAN2023 Lupus Test - Negative
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Zyrtec; Allegra; Excedrin
- Allergien
- Sumatriptan; Sulfa
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 86,0
- Geschlecht
- F
- Eingang
- 24.01.2023
- Impfdatum
- 06.11.2022
- Beginn
- 16.01.2023
- Tage bis Beginn
- 71,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
unable to interview case due to hospitalization
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- Unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 23.12.2022
- Impfdatum
- 01.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Confusional state
Electrocardiogram
Full blood count
Urine analysis
Symptomtext
Confusion; observed in ER for 2-3 hours; no treatment
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Confusional state
- Hospital-Tage
- -
- Labordaten
- CBC, UA, ECG
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetes, hypertension, gout, high cholesterol, eczema, low vitamin B 12 level, arthritis
- Andere Medikamente
- Allopurinoal atenolol lisinopril simvastatin aspirin omega-3 metformin humulin omeprazole fluticasone vitamin D vitamin B12 one-a-day vitamin calcium
- Allergien
- lobster, shrimp, lipitor
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.12.2022
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
2 Adult patients received Monovalent shots on 13MAY2022 from vial shipped in 02MAR2022 and thawed in a cooler while being transported; No adverse event; Received expired monovalent vaccine after 30-day Use By Date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired monovalent vaccine after 30-day Use By Date), PRODUCT STORAGE ERROR (2 Adult patients received Monovalent shots on 13MAY2022 from vial shipped in 02MAR2022 and thawed in a cooler while being transported) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 13-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired monovalent vaccine after 30-day Use By Date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (2 Adult patients received Monovalent shots on 13MAY2022 from vial shipped in 02MAR2022 and thawed in a cooler while being transported) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received expired monovalent vaccine after 30-day Use By Date), PRODUCT STORAGE ERROR (2 Adult patients received Monovalent shots on 13MAY2022 from vial shipped in 02MAR2022 and thawed in a cooler while being transported) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Received expired monovalent vaccine after 30-day Use By Date) and PRODUCT STORAGE ERROR (2 Adult patients received Monovalent shots on 13MAY2022 from vial shipped in 02MAR2022 and thawed in a cooler while being transported). Concomitant medication was not reported. Patient received Monovalent vaccine on 13-May-2022 Lot 046L21A which was shipped on 02-MAR-2022 and thawed in a cooler while being transported. Vial did not undergo any temperature excursions. Treatment medication was not reported. This case is for patient 1 from 2 adult patients who received vaccine on 13-May-2022 from vial shipped in 02-Mar-2022. This case was linked to US-MODERNATX, INC.-MOD-2022-682174, US-MODERNATX, INC.-MOD-2022-682176, US-MODERNATX, INC.-MOD-2022-682173 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 02-Dec-2022: Live follow up received. Contain no new information.; Sender's Comments: US-MODERNATX, INC.-MOD-2022-682174:Monovalent (Same reporter) US-MODERNATX, INC.-MOD-2022-682176:Monovalent (Same reporter) US-MODERNATX, INC.-MOD-2022-682173:Patient 2 from 2 Adult patients received Monovalent shots on 13MAY2022, master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.12.2022
- Impfdatum
- 06.05.2022
- Beginn
- 06.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
1 patient received Monovalent shot on 06-May-2022 from vial shipped in 02-Mar-2022 and thawed in a cooler while being transported; No adverse event; Received Expired Monovalent vaccine after 30-day Use By Date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date), PRODUCT STORAGE ERROR (1 patient received Monovalent shot on 06-May-2022 from vial shipped in 02-Mar-2022 and thawed in a cooler while being transported) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 06-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 06-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (1 patient received Monovalent shot on 06-May-2022 from vial shipped in 02-Mar-2022 and thawed in a cooler while being transported) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date), PRODUCT STORAGE ERROR (1 patient received Monovalent shot on 06-May-2022 from vial shipped in 02-Mar-2022 and thawed in a cooler while being transported) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date) and PRODUCT STORAGE ERROR (1 patient received Monovalent shot on 06-May-2022 from vial shipped in 02-Mar-2022 and thawed in a cooler while being transported). Concomitant medication was not reported. Patient received Monovalent vaccine on 06-May-2022 Lot 046L21A which was shipped on 02-MAR-2022 and thawed in a cooler while being transported. Vial did not undergo any temperature excursions. Vial size 5.5 ml red cap. Reporter stated that, since they did not notice the vaccine was expired, some of these patients received another Monovalent dose after the expired dose within recommended time. They are still investigating and does not have any patient identifiers at this point. Treatment medication was not reported. This case was linked to MODERNATX, INC.-MOD-2022-682174, MODERNATX, INC.-MOD-2022-682176, MODERNATX, INC.-MOD-2022-682038 (E2B Linked Report). Most recent FOLLOW-UP information incorporated above includes: On 02-Dec-2022: Live follow up added. Reporter added and narrative updated.; Sender's Comments: MODERNATX, INC.-MOD-2022-682174:Monovalent (Same reporter) MODERNATX, INC.-MOD-2022-682176:Monovalent (Same reporter) MODERNATX, INC.-MOD-2022-682038:Same reporter case/master case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.12.2022
- Impfdatum
- 06.04.2022
- Beginn
- 06.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
1 patient received Monovalent shot on 06-Apr-2022 from vial shipped in 02-Mar-2022 and thawed in a cooler while being transported; No adverse event; Received Expired Monovalent vaccine after 30-day Use By Date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date), PRODUCT STORAGE ERROR (1 patient received Monovalent shot on 06-Apr-2022 from vial shipped in 02-Mar-2022 and thawed in a cooler while being transported) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 06-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 06-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (1 patient received Monovalent shot on 06-Apr-2022 from vial shipped in 02-Mar-2022 and thawed in a cooler while being transported) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date), PRODUCT STORAGE ERROR (1 patient received Monovalent shot on 06-Apr-2022 from vial shipped in 02-Mar-2022 and thawed in a cooler while being transported) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date) and PRODUCT STORAGE ERROR (1 patient received Monovalent shot on 06-Apr-2022 from vial shipped in 02-Mar-2022 and thawed in a cooler while being transported). Concomitant medication was not reported. Patient received Monovalent vaccine on 06-Apr-2022 Lot 046L21A which was shipped on 02-MAR-2022 and thawed in a cooler while being transported. Vial did not undergo any temperature excursions. Vial size 5.5 ml red cap. Reporter stated that, since they did not notice the vaccine was expired, some of these patients received another Monovalent dose after the expired dose within recommended time. They are still investigating and does not have any patient identifiers at this point. Treatment medication was not reported. Most recent FOLLOW-UP information incorporated above includes: On 02-Dec-2022: Live Significant Follow-up received: Reporter added and narrative updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 07.12.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Vaccine was stored in the refrigerator on 02-Mar-2022, patient received Monovalent shots on 04-Apr-2022; No adverse event; Received Expired Monovalent vaccine after 30-day Use By Date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date), PRODUCT STORAGE ERROR (Vaccine was stored in the refrigerator on 02-Mar-2022, patient received Monovalent shots on 04-Apr-2022) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 04-Apr-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 04-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was stored in the refrigerator on 02-Mar-2022, patient received Monovalent shots on 04-Apr-2022) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date), PRODUCT STORAGE ERROR (Vaccine was stored in the refrigerator on 02-Mar-2022, patient received Monovalent shots on 04-Apr-2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date) and PRODUCT STORAGE ERROR (Vaccine was stored in the refrigerator on 02-Mar-2022, patient received Monovalent shots on 04-Apr-2022). No concomitant medications were reported. The vial could be either from individual vials or unbroken cartons and was of the size of 2.5 ml. 1 Adult patient received Monovalent shots on 04-APR-2022 from vial shipped in 02-MAR-2022 thawed in a cooler while being transported. The vial did not undergo any temperature excursions. Treatment information was not provided. This case was for adult patient who received monovalent dose on 04-Apr-2022, as described by the reporter. Most recent FOLLOW-UP information incorporated above includes: On 02-Dec-2022: Live Significant follow up received: Reporter added and narrative updated.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 06.12.2022
- Impfdatum
- 13.05.2022
- Beginn
- 13.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
Symptomtext
Received Expired Monovalent vaccine after 30-day Use By Date; No adverse event; Received Expired Monovalent vaccine after 30-day Use By Date; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date), PRODUCT STORAGE ERROR (Received Expired Monovalent vaccine after 30-day Use By Date) and NO ADVERSE EVENT (No adverse event) in an adult patient of an unknown gender who received mRNA-1273 (Spikevax) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 13-May-2022, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 13-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Received Expired Monovalent vaccine after 30-day Use By Date) and NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date), PRODUCT STORAGE ERROR (Received Expired Monovalent vaccine after 30-day Use By Date) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Received Expired Monovalent vaccine after 30-day Use By Date) and PRODUCT STORAGE ERROR (Received Expired Monovalent vaccine after 30-day Use By Date). No concomitant medication was reported. HCP reported that some adult patients received expired doses of both Mono and Bivalent vials of Moderna COVID-19 vaccine after 30-day Use By Date. Vials were mix of individual vials or unbroken cartons of size 5.5 ml red cap and 2.5 ml bivalent. Reporter asked if the vials were viable and was there a need to revaccinate. On 02-Mar-2022, the monovalent vial (lot- 046L21A) was shipped and thawed in a cooler while being transported. The vial did not undergo any temperature excursions. Reporter did not notice the vaccine was expired, some of these patients received another Monovalent dose after the expired dose within recommended time. This case is about patient 2 out of 2 adult patients who received monovalent shots on 13-May-2022 from vial shipped in 02-Mar-2022. No treatment medication was reported. This case was linked to US-MODERNATX, INC.-MOD-2022-682174, US-MODERNATX, INC.-MOD-2022-682176 (Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-682174:Monovalent (Same reporter) US-MODERNATX, INC.-MOD-2022-682176:Monovalent (Same reporter)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 87,0
- Geschlecht
- F
- Eingang
- 13.09.2022
- Impfdatum
- 10.04.2022
- Beginn
- 05.09.2022
- Tage bis Beginn
- 148,0
- Dosis
- 4
- 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 after 4 vaccines Pfizer 3/11/21 Lot# EN6207; Pfizer 4/1/21 Lot# Er8732; Pfizer 10/6/21 Lot# 301308A; Moderna 4/10/22 Lot# 046L21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID +
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 02.09.2022
- Impfdatum
- 31.03.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 27.08.2022
- Impfdatum
- 31.03.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 4,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 30.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Administered the vaccine from a vial that was open on 01-Jun-2022 stored in the refrigerator on same day and administered on 27-Jul-2022; Administered the vaccine from a vial that was open on 01-Jun-2022 stored in the refrigerator on same day and administered on 27-Jul-2022; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered the vaccine from a vial that was open on 01-Jun-2022 stored in the refrigerator on same day and administered on 27-Jul-2022) and PRODUCT STORAGE ERROR (Administered the vaccine from a vial that was open on 01-Jun-2022 stored in the refrigerator on same day and administered on 27-Jul-2022) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 prophylaxis. It was unknown if the patient had medications, food and other products allergy. Medical history reported relating to mentioned AE and both Acute and Chronic illnesses at the time of vaccination was unknown. It was unknown if the patient had ever been diagnosed or tested positive for COVID-19. It was unknown whether any other vaccines were given within 1 month prior to Moderna COVID-19 vaccine. Previously administered products included for Product used for unknown indication: Jhonson & Johson (First booster) on 28-Nov-2021, Jhonson & Johson (Primary series:2) and Jhonson & Johson (Primary series:1). Past adverse reactions to the above products included No adverse event with Jhonson & Johson, Jhonson & Johson and Jhonson & Johson. On 27-Jul-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered the vaccine from a vial that was open on 01-Jun-2022 stored in the refrigerator on same day and administered on 27-Jul-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Administered the vaccine from a vial that was open on 01-Jun-2022 stored in the refrigerator on same day and administered on 27-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered the vaccine from a vial that was open on 01-Jun-2022 stored in the refrigerator on same day and administered on 27-Jul-2022) and PRODUCT STORAGE ERROR (Administered the vaccine from a vial that was open on 01-Jun-2022 stored in the refrigerator on same day and administered on 27-Jul-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Patient received the second booster dose on 27-Jul-2022. It was unknown whether adverse event cause patient to seek medical care. The patient did not experienced a similar event in the past. The vial did not undergo any temperature excursions. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if the patient had medications, food and other products allergy. Medical history reported relating to mentioned AE and both Acute and Chronic illnesses at the time of vaccination was unknown. It was unknown if the patient had ever been diagnosed or tested positive for COVID-19. It was unknown whether any other vaccines were given within 1 month prior to Moderna COVID-19 vaccine.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 30.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Administered the vaccine from a vial that was open on 01-Jun-2022 stored in the refrigerator on same day and administered on 27-Jul-2022; administer the vaccine from a vial that was open on 1Jun2022 to 6 patients; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (administer the vaccine from a vial that was open on 1Jun2022 to 6 patients) and PRODUCT STORAGE ERROR (Administered the vaccine from a vial that was open on 01-Jun-2022 stored in the refrigerator on same day and administered on 27-Jul-2022) in a 29-year-old male patient who received mRNA-1273 (Spikevax) (batch no. 046L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 27-Jul-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 27-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (administer the vaccine from a vial that was open on 1Jun2022 to 6 patients). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Administered the vaccine from a vial that was open on 01-Jun-2022 stored in the refrigerator on same day and administered on 27-Jul-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (administer the vaccine from a vial that was open on 1Jun2022 to 6 patients) and PRODUCT STORAGE ERROR (Administered the vaccine from a vial that was open on 01-Jun-2022 stored in the refrigerator on same day and administered on 27-Jul-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. Patient has no known allergies. No concomitant medication were reported. The vial was initially stored in the refrigerator on 1Jun2022and was opened on the same day. The vial didn't undergo any temperature excursions. No treatment information were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 28.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product storage error
Symptomtext
The patient has not reported any adverse reactions. On 6/1/2022 a vial was used for COVID clinic. After use, the vial was placed in the refrigerator (this should have been wasted after 12 hours). On 07/27/2022, the vial was taken out of the fridge and used for this patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Acquired coagulation factor deficiency, hyperlipidemia, Essential hypertension, Hepatitis C.
- Vorgeschichte
- Acquired coagulation factor deficiency, hyperlipidemia, Essential hypertension, Hepatitis C.
- Andere Medikamente
- Aspirin 81mg daily, Hydrochlorothiazide 12.5mg daily, Nitroglycerin Sublingual prn
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 28.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Wrong technique in product usage process
Symptomtext
The patient has not reported any adverse reactions. On 6/1/2022 a vial was used for COVID clinic. After use, the vial was placed in the refrigerator (this should have been wasted after 12 hours). On 07/27/2022, the vial was taken out of the fridge and used for this patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Alcohol use disorder, cannabis use disorder,
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No known drug allergies
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 28.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
The patient has not reported any adverse reactions. On 6/1/2022 a vial was used for COVID clinic. After use, the vial was placed in the refrigerator (this should have been wasted after 12 hours). On 07/27/2022, the vial was taken out of the fridge and used for this patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 28.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Wrong technique in product usage process
Symptomtext
The patient has not reported any adverse reactions. On 6/1/2022 a vial was used for COVID clinic. After use, the vial was placed in the refrigerator (this should have been wasted after 12 hours). On 07/27/2022, the vial was taken out of the fridge and used for this patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- No Known allergies
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 28.07.2022
- Impfdatum
- 27.07.2022
- Beginn
- 27.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
The patient has not reported any adverse reactions. On 6/1/2022 a vial was used for COVID clinic. After use, the vial was placed in the refrigerator (this should have been wasted after 12 hours). On 07/27/2022, the vial was taken out of the fridge and used for this patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, unspecified thrombocytopenia, enthesopathy of the knee
- Andere Medikamente
- Hydrochlorothiazide 25mg daily, Amlodipine 5mg daily
- Allergien
- No Known allergies
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 23.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 12.07.2022
- 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
gave 4 doses that were expired; vial was initially stored in the refrigerator on 12-Jul-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (gave 4 doses that were expired) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 12-Jul-2022) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 13-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Jul-2022, the patient experienced PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 12-Jul-2022). On 13-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (gave 4 doses that were expired). At the time of the report, EXPIRED PRODUCT ADMINISTERED (gave 4 doses that were expired) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 12-Jul-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. No temperature excursions was reported. The vial was initially stored in the refrigerator on 12-Jul-2022. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- 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
Doses were expired 06Jul2022, Date the vial was initially stored in the refrigerator was on 12Jul2022; Gave 4 doses that were expired; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Gave 4 doses that were expired) and PRODUCT STORAGE ERROR (Doses were expired 06Jul2022, Date the vial was initially stored in the refrigerator was on 12Jul2022) in a 74-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 13-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Gave 4 doses that were expired). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Doses were expired 06Jul2022, Date the vial was initially stored in the refrigerator was on 12Jul2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Gave 4 doses that were expired) and PRODUCT STORAGE ERROR (Doses were expired 06Jul2022, Date the vial was initially stored in the refrigerator was on 12Jul2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided. Reporter was wondering what will be the process because last week they had a clinic, and they realized the doses were expired on 06-Jul-2022 and on 12-Jul-2022, the vials were initially stored in the refrigerator. On 13Jul2022, they gave 4 booster doses that were expired, and reporter was confused about the expiration date. The vial did not undergone any temperature excursions. No treatment medications were reported. This case was linked to US-MODERNATX, INC.-MOD-2022-609300, US-MODERNATX, INC.-MOD-2022-609296, US-MODERNATX, INC.-MOD-2022-609298 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-609300:Same reporter case US-MODERNATX, INC.-MOD-2022-609296:Same reporter case US-MODERNATX, INC.-MOD-2022-609298:Same reporter case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- 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
Doses were expired 06 Jul 2022, Date the vial was initially stored in the refrigerator was on 12 Jul 2022; Gave 4 doses that were expired; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Gave 4 doses that were expired) and PRODUCT STORAGE ERROR (Doses were expired 06 Jul 2022, Date the vial was initially stored in the refrigerator was on 12 Jul 2022) in a 76-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 13-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 13-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Gave 4 doses that were expired). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Doses were expired 06 Jul 2022, Date the vial was initially stored in the refrigerator was on 12 Jul 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Gave 4 doses that were expired) and PRODUCT STORAGE ERROR (Doses were expired 06 Jul 2022, Date the vial was initially stored in the refrigerator was on 12 Jul 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Date the vial was initially stored in the refrigerator was on 12-Jul-2022. The vial did not undergo any temperature excursions. Patient was administered with booster dose. (Not specified first or second booster dose) No treatment information was reported. This case was linked to US-MODERNATX, INC.-MOD-2022-609299, US-MODERNATX, INC.-MOD-2022-609300, US-MODERNATX, INC.-MOD-2022-609296 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-609299: US-MODERNATX, INC.-MOD-2022-609300: US-MODERNATX, INC.-MOD-2022-609296:
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 23.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 12.07.2022
- 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
gave 4 doses that were expired; vial was initially stored in the refrigerator on 12Jul2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (gave 4 doses that were expired) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 12Jul2022) in a 59-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 13-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Jul-2022, the patient experienced PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 12Jul2022). On 13-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (gave 4 doses that were expired). At the time of the report, EXPIRED PRODUCT ADMINISTERED (gave 4 doses that were expired) and PRODUCT STORAGE ERROR (vial was initially stored in the refrigerator on 12Jul2022) 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 patient was administered with booster dose. The vial did not undergo any temperature excursions. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 23.07.2022
- Impfdatum
- 14.07.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was stored beyond its expiry date; Gave a vaccine that expired 06July2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Gave a vaccine that expired 06July2022) and PRODUCT STORAGE ERROR (Vaccine was stored beyond its expiry date) in a 20-year-old female patient who received mRNA-1273 (Spikevax) (batch no. 046L21A) for COVID-19 prophylaxis. No Medical History information was reported. On 14-Jul-2022, the patient received second dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 14-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Gave a vaccine that expired 06July2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was stored beyond its expiry date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Gave a vaccine that expired 06July2022) and PRODUCT STORAGE ERROR (Vaccine was stored beyond its expiry date) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. The vial was initially stored in the refrigerator on 22-Jun-2022. The vial does not undergone any temperature excursions. No treatment medications was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 17.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 18.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Administered expired booster dose to patient. Moderna Vial expired on 7/06/22 and administered dose on 7/13/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Administered expired booster dose to patient. Moderna Vial expired on 7/06/22 and administered dose on 7/13/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Administered expired booster dose to patient. Moderna Vial expired on 7/06/22 and administered dose on 7/13/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 18.07.2022
- Impfdatum
- 13.07.2022
- Beginn
- 13.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Administered expired booster dose to patient. Moderna Vial expired on 7/06/22 and administered dose on 7/13/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 17.07.2022
- Impfdatum
- 13.04.2022
- Beginn
- 01.06.2022
- Tage bis Beginn
- 49,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Electrocardiogram abnormal
Heart rate irregular
Ventricular extrasystoles
Symptomtext
At routine check-up, irregular hearbeat noted. Also noted at urgent care visit later that month (for Covid.) EKG showed PVC. Reportedly not life-threatening, but have never been told of heartbeat irregularity before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electrocardiogram abnormal
- Hospital-Tage
- -
- Labordaten
- EKG 6/1/22 Additional cardio tests scheduled for 8/1/22.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism, depression, ADHD, Osteopenia, IBS
- Andere Medikamente
- Fluoxitene, Methylamphetamine ER, Levothryroxin, Vitamin D, Vivical, Citrucel
- Allergien
- Erythromycin
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 20,0
- Geschlecht
- F
- Eingang
- 15.07.2022
- Impfdatum
- 14.07.2022
- Beginn
- 14.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
No adverse event
Symptomtext
Vaccine expiration date 07/06/2022. No adverse reactions noted
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 15.07.2022
- Impfdatum
- 08.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 20,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 12.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Vaccination error
Symptomtext
Pt administered expired Moderna vaccine LOT: 046L21A EXP: 7/6/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none listed. pt's first visit at time of vaccine error
- Vorgeschichte
- pt's first visit at time of vaccine error
- Andere Medikamente
- none listed
- Allergien
- none on file
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 12.07.2022
- Impfdatum
- 12.07.2022
- Beginn
- 12.07.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Expired vaccine administered. No adverse event observed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 06.07.2022
- Impfdatum
- 01.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood glucose increased
Diabetes mellitus inadequate control
Glycosylated haemoglobin
Symptomtext
I am a long term diabetic. This booster and the one before spiked my blood sugar. The next day my blood sugar was 400. Since then, mu blood sugar has been high and hard for me to get under control. I have been working with my Endocrinologist and she has prescribed some medications but we have not found a solution. It has been a constant struggle to get my blood sugar down. My doctor has seen this before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood glucose increased
- Hospital-Tage
- -
- Labordaten
- A1C- Tested Regularly
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension; Diabetes
- Andere Medikamente
- Carbedilol; Torsemide; Jardiance; Basaglar; Olmesartan; Advil
- Allergien
- Penicillin; Keflex
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 08.06.2022
- Impfdatum
- 10.02.2021
- Beginn
- 27.04.2022
- Tage bis Beginn
- 441,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Confirmed Breakthrough Case COVID-19 (Moderna) 1 09/02/2021 Clinic Moderna 037B21A COVID-19 (Moderna) 2 02/10/2022 Clinic Moderna 046L21A
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Postive Covid Test - 4/27/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 04.06.2022
- Impfdatum
- 10.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 10,0
- Dosis
- 4
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Symptomtext
See item 11. No adverse event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- I am filing this report to correct the misunderstanding that I had an adverse effect fron the moderna dose 4 vaccine. I DID NOT HAVE ADVERSE EFFECT. I did get covid shortly after the vaccine and thought this vsafe app might be collecting that info but I was mistaken.
- Vorgeschichte
- See item 11
- Andere Medikamente
- See item 11.
- Allergien
- See item 11.
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 31.03.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Drug ineffective
Symptomtext
Treatment of COVID-19; Treatment of COVID-19; This is a spontaneous report received from contactable reporter(s) (Consumer or other non HCP). The reporter is the patient. A 71-year-old female patient (not pregnant) received BNT162b2 (BNT162B2), on 31Mar2022 as dose number unknown, single (Batch/Lot number: unknown) at the age of 71 years, in left arm for covid-19 immunisation. The patient's relevant medical history and concomitant medications were not reported. The following information was reported: DRUG INEFFECTIVE (medically significant), COVID-19 (medically significant), outcome "unknown" and all described as "Treatment of COVID-19". Therapeutic measures were taken as a result of drug ineffective, covid-19. Clinical information: Moderna Lot: 046L21A. Other medical history: No chronic health conditions. The information on the batch/lot number for BNT162b2 has been requested and will be submitted if and when received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.05.2022
- Tage bis Beginn
- 61,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Symptomtext
COVID-19/ cough/ not feeling so good; This spontaneous case was reported by a physician and describes the occurrence of COVID-19 (COVID-19/ cough/ not feeling so good) in an 80-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. Concurrent medical conditions included Allergy. In March 2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In May 2022, the patient experienced COVID-19 (COVID-19/ cough/ not feeling so good). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 11-May-2022 to 16-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, COVID-19 (COVID-19/ cough/ not feeling so good) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): In May 2022, SARS-CoV-2 test: negative (Negative) Negative, negative (Negative) Negative and. On 15-May-2022, SARS-CoV-2 test positive (Positive) Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided. It was reported that the patient did not take any other medications/products within 2 weeks of starting COVID-19 treatment. It was reported that 5 days after completing treatment of Paxlovid patient was feeling good. Patient even had two negative PCR tests. 6 or 7 days later patient reported that it started with a cough, not feeling so good and had a positive rapid and PCR test.. Device date: 23-May-2022 Company Comment: This is a spontaneous case concerning an 80-year-old male patient with no relevant medical history, who experienced the unexpected, non-serious adverse event of special interest of COVID-19, approximately 2 months after receiving a dose of mRNA-1273 vaccine. The patient was treated with Nirmatrelvir/Ritonavir for 5 days and tested negative to PCR test after treatment completion. Approximately 6-7 days after the treatment, patient reported to develop a cough, did not feel good and tested positive in rapid and PCR test. The event had not resolved at the time of the report. It should be noted that the dose was reported as fourth dose however, there were no information regarding the previous 3 doses of COVID-19 vaccine. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This is a spontaneous case concerning an 80-year-old male patient with no relevant medical history, who experienced the unexpected, non-serious adverse event of special interest of COVID-19, approximately 2 months after receiving a dose of mRNA-1273 vaccine. The patient was treated with Nirmatrelvir/Ritonavir for 5 days and tested negative to PCR test after treatment completion. Approximately 6-7 days after the treatment, patient reported to develop a cough, did not feel good and tested positive in rapid and PCR test. The event had not resolved at the time of the report. It should be noted that the dose was reported as fourth dose however, there were no information regarding the previous 3 doses of COVID-19 vaccine. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 202205; Test Name: postive rapid and PCR test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 202205; Test Name: postive rapid and PCR test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220515; Test Name: postive rapid and PCR test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 31.05.2022
- Impfdatum
- 24.03.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 46,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Symptomtext
Return of symptoms; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (Return of symptoms) in a 43-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. Co-suspect product included non-company product NIRMATRELVIR, RITONAVIR (PAXLOVID) for COVID-19 treatment. Concurrent medical conditions included Thyroid cancer. On 24-Mar-2022 at 5:00 PM, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Apr-2022, the patient started NIRMATRELVIR, RITONAVIR (PAXLOVID) (unknown route) at an unspecified dose. On 09-May-2022 at 7:00 PM, the patient experienced COVID-19 (Return of symptoms). At the time of the report, COVID-19 (Return of symptoms) was resolving. Concomitant medications were not reported. The patient did not took any other medications/products within 2 weeks of starting COVID-19 treatment. Patient previously received a COVID-19 Vaccine. On 09May2022 Return of symptoms. Patient treated with antibiotic and device date was 24May2022. Company comment: This spontaneous case concerns a 43 year old female patient, with relevant medical history of micropapillary thyroid cancer, who experienced the unexpected non serious AESI of COVID-19, unknown days after receiving the fourth dose of mRNA-1273 vaccine in the COVID-19 vaccination series. The patient took Paxlovid for COVID-19 for 5 days. However, symptoms returned after about 9 days. The event was resolving. No further details on the previous doses of vaccination and COVID-19 test dates before and after Paxlovid treatment were available in the report. Medical history of micropapillary thyroid cancer and the ongoing COVID-19 pandemic could be risk factors for the event. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case concerns a 43 year old female patient, with relevant medical history of micropapillary thyroid cancer, who experienced the unexpected non serious AESI of COVID-19, unknown days after receiving the fourth dose of mRNA-1273 vaccine in the COVID-19 vaccination series. The patient took Paxlovid for COVID-19 for 5 days. However, symptoms returned after about 9 days. The event was resolving. No further details on the previous doses of vaccination and COVID-19 test dates before and after Paxlovid treatment were available in the report. Medical history of micropapillary thyroid cancer and the ongoing COVID-19 pandemic could be risk factors for the event. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Thyroid cancer
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 26.05.2022
- Impfdatum
- 26.05.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Wrong product administered
Symptomtext
Vaccine administration error - patient requested Pfizer for 2nd booster (in those >50 yo) but was accidentally given Moderna 0.5ml instead at approximately 11:23am by the medical assistant vaccine administrator. Patient previously received Pfizer for her primary series (1/28/21 first dose, 2/17/21 second dose) and Pfizer for her first booster (10/29/21). The clinical pharmacist preparing the vaccines that day reached out to patient at approximately 1:30pm to notify patient of the administration error. Patient was informed that mixing of matching of Moderna & Pfizer brands is allowed per CDC recommendations. All questions and concerns from patient regarding vaccine boosters were answered by the clinical pharmacist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 18.02.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 41,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling abnormal
Nasal discomfort
Respiratory tract congestion
Throat irritation
Symptomtext
I had a sensation of coming down with a cold. Scratchy throat, irritated nose, and congestion that lasted 2-3 days. It wasn't severe, so I didn't associate it with Covid, however, it did feel worse than my normal allergies. My symptoms cleared up within a few days on their own.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling abnormal
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Levoxyl Paxil Multivitamin Turmeric
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 19.05.2022
- Impfdatum
- 16.05.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vial was exposed to room temperature for 73-74 hours; The vial was first punctured on 13-May-2022 and administered on 16-May-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vial was first punctured on 13-May-2022 and administered on 16-May-2022) and PRODUCT STORAGE ERROR (The vial was exposed to room temperature for 73-74 hours) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 16-May-2022 at 9:28 AM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 16-May-2022 at 9:28 AM, after starting mRNA-1273 (Spikevax), the patient experienced EXPIRED PRODUCT ADMINISTERED (The vial was first punctured on 13-May-2022 and administered on 16-May-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was exposed to room temperature for 73-74 hours). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vial was first punctured on 13-May-2022 and administered on 16-May-2022) and PRODUCT STORAGE ERROR (The vial was exposed to room temperature for 73-74 hours) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. The reporter stated that a vial of Moderna vaccine was punctured on 13-May-2022 and it was pulled out on 16-May-2022 and punctured to administer a few doses. On 13-May-2022, the vial was initially stored in the refrigerator. On 13-May-2022 at 08:00 AM time, the vial was first punctured. The vaccine was administered on 16-May-2022 at 9:28 AM Pacific time to the patient. The vial was stored in the room temperature post puncture. Reportedly, the vial didn't undergo any temperature excursions and the total amount of time the vial exposed to room temperature range (8? to 25?C= 46? to 77?F) was 73-74 hours. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 18.05.2022
- Impfdatum
- 16.05.2022
- Beginn
- 16.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vial was exposed to room temperature for 73-74 hours; The vial was first punctured on 13-May-2022 and administered on 16-May-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vial was first punctured on 13-May-2022 and administered on 16-May-2022) and PRODUCT STORAGE ERROR (The vial was exposed to room temperature for 73-74 hours) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 16-May-2022 at 9:15 AM, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 16-May-2022 at 9:15 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vial was first punctured on 13-May-2022 and administered on 16-May-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was exposed to room temperature for 73-74 hours). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vial was first punctured on 13-May-2022 and administered on 16-May-2022) and PRODUCT STORAGE ERROR (The vial was exposed to room temperature for 73-74 hours) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. The vial was initially stored in the refrigerator on 13-May-2022. It was first punctured on 13-May-2022 at 8.00 am Pacific Time and was stored at room temperature post puncture. The vial did not undergo any temperature excursions. The total amount of time the vial was exposed to room temperature range 8 degree Celsius to 25 degree Celsius was 73-74 hours. No treatment information was reported. Most recent FOLLOW-UP information incorporated above includes: On 16-May-2022: Follow up received. Added reporter, expiry date and time of Spikevax administration and updated lot number.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 17.05.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Vaccine approved for 18 years of age and older was given to a 17 year old patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 12.05.2022
- Impfdatum
- 02.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
Patient was given .5ml of Moderna vaccine instead of .25 ml for 2nd covid booster. No adverse reactions reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HIV, coronary arteriosclerosis, chronic hepatitis
- Andere Medikamente
- ammonium lactate lotion ascorbic acid (vitamin C) atenolol B-6 Biktarvy clobetasol cyanocobalamin (vitamin B-12) Eliquis hydrocodone-acetaminophen Multiple Vitamin-Minerals pravastatin tadalafil tramadol triamcinolone acetonide Vitamin C Vi
- Allergien
- Statins, sulfa
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 11.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Patient was given .5ml of Moderna vaccine instead of .25ml for 2nd covid booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- cardiomyopathy, congestive heart failure
- Andere Medikamente
- Asprin Ec; azelastine; carvedilol; cholecalciferol; ferrous sulfate; furosemide; Lasix; losartan; multivitamin; omeprazole; paroxetine; zinc gluconate
- Allergien
- Aleve, lisinopril, naproxen
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 07.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Patient was given .5ml of Moderna vaccine instead of .25ml for 2nd covid booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- bisacodyl; ciclopirox; hydroxyzine; levothyroxine; lisinopril; polyethylene glycol
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 09.05.2022
- Impfdatum
- 09.05.2022
- Beginn
- 09.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
The nurse who administered the vaccine was looking at the wrong paperwork and she administered a .25 dose instead of a .5 dose for his primary dose. By the time she realized it, the client was gone. I have tried calling him but, his voicemail is full so, I will continue to try and get in touch with him to get him back for another .25 dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 07.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Moderna COVID-19 vaccine administered on 04-May-2022 was initially stored in the refrigerator on 01-Apr-2022; expiration date of 01-May-2022 but doses were given 04-May-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expiration date of 01-May-2022 but doses were given 04-May-2022) and PRODUCT STORAGE ERROR (Moderna COVID-19 vaccine administered on 04-May-2022 was initially stored in the refrigerator on 01-Apr-2022) in a 70-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 04-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expiration date of 01-May-2022 but doses were given 04-May-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Moderna COVID-19 vaccine administered on 04-May-2022 was initially stored in the refrigerator on 01-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expiration date of 01-May-2022 but doses were given 04-May-2022) and PRODUCT STORAGE ERROR (Moderna COVID-19 vaccine administered on 04-May-2022 was initially stored in the refrigerator on 01-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not reported. Date the vial was initially stored in the refrigerator: 01-Apr-2022. Vial did not undergo any temperature excursions. It was started that the patient has not called to report any adverse events. Treatment medications were not provided. This case was linked to MOD-2022-558234 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 04-May-2022: The follow up information received contains no new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 07.05.2022
- Impfdatum
- 04.05.2022
- Beginn
- 04.05.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vial was initially stored in the refrigerator on 01-APR-2022 and administered on 04-MAY-2022; expiration date of 01-May-2022 but doses were given today 04-May-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (expiration date of 01-May-2022 but doses were given today 04-May-2022) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 01-APR-2022 and administered on 04-MAY-2022) in a 69-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 04-May-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 04-May-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (expiration date of 01-May-2022 but doses were given today 04-May-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 01-APR-2022 and administered on 04-MAY-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (expiration date of 01-May-2022 but doses were given today 04-May-2022) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 01-APR-2022 and administered on 04-MAY-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported by reporter. The vial was initially stored in the refrigerator on 01-APR-2022. The vial did not undergo any temperature excursions. It was reported that patient have not called to report any adverse events No treatment medications were reported by reporter. This case was linked to MOD-2022-558253 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 04-May-2022: Source document contains no new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 05.05.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Symptomtext
This third dose was mistakenly given early. Our team believed this was his 2nd dose, but later learned that he had previously received 2 doses, making this his third dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 05.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Vaccination site bruising
Symptomtext
Bruising directly above the injection site (left arm); This spontaneous case was reported by a consumer and describes the occurrence of VACCINATION SITE BRUISING (Bruising directly above the injection site (left arm)) in a 65-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: J and J (1st dose with lot number 1805029) on 15-Mar-2021, FLU VACCINE VII in October 2021 and PFIZER BIONTECH COVID-19 VACCINE (1st booster dose with lot number 301358A) on 29-Oct-2021. Past adverse reactions to the above products included No adverse event with FLU VACCINE VII, J and J and PFIZER COVID-19 VACCINE. Concurrent medical conditions included Diabetes (She takes metformin, glipizide and pioglita for diabetes) and Drug allergy (Allergies to Codeine, Demerol and Hydrocodone.). Concomitant products included METFORMIN, GLIMEPIRIDE (GLIPIRIDE) and PIOGLITAZONE HYDROCHLORIDE (PIOGLITA) for Diabetes. On 15-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 15-Apr-2022, the patient experienced VACCINATION SITE BRUISING (Bruising directly above the injection site (left arm)). At the time of the report, VACCINATION SITE BRUISING (Bruising directly above the injection site (left arm)) was resolving. The patient had no COVID-19 diagnosis prior to or after getting the Covid-19 vaccines. The patient reported bruising directly above the injection site on the left arm after getting the Moderna Covid-19 vaccine for her 2nd booster dose.. At the time of report it was resolving.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Vaccination site bruising
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Diabetes (She takes metformin, glipiride and pioglita for diabetes); Drug allergy (Allergies to Codeine, Demerol and Hydrocodeine.)
- Vorgeschichte
- -
- Andere Medikamente
- METFORMIN; GLIPIRIDE; PIOGLITA
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 04.05.2022
- Impfdatum
- 01.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 14,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear discomfort
Labyrinthitis
SARS-CoV-2 test negative
Symptomtext
My left ear became clogged like I was under water and I had resulting pressure heads behind my ear. When I went to see the doctor he gave me antibiotics saying that it may be an inner ear infection, I took the full course and still have minor symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Ear discomfort
- Hospital-Tage
- -
- Labordaten
- COVID PCR test- negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 25.04.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 27.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 26.04.2022
- Tage bis Beginn
- 26,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Dry throat
Ear discomfort
Head discomfort
SARS-CoV-2 test positive
Symptomtext
We were walking with a group of 10 people. We came back Monday, I had to be tested on Sunday by the authorities with a negative result before we could fly. I felt like I had a dry throat, a stuffed head and my ears did not pop, my head was absolutely full. We flew all day Monday and we got home Tuesday. I thought we that flying all day and maybe this was a result. I had more jet lag than typically, sluggish, a dry throat, stuffed head. It was a long flight, so I thought I would give it a day. I took a COVID-19 test yesterday and that came back positive. I had a virtual visit with my doctor today and he prescribe Paxlovid. Since returning in the last day I have heard from other travelers that have also tested positive. - 4 of the 10 people have tested positive.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Home test - positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Baby Aspirin; Calcium w/ Vitamin D; Collagen
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental overdose
Expired product administered
Product storage error
Symptomtext
Vaccine was administered to patient 2 days past the 30-day time in refrigerator; Dose/volume 0.5 ml/Patient received Moderna vaccine Booster on 04/08/2022; Vaccine was given beyond use date; This spontaneous case was reported by a nurse and describes the occurrence of PRODUCT STORAGE ERROR (Vaccine was administered to patient 2 days past the 30-day time in refrigerator), ACCIDENTAL OVERDOSE (Dose/volume 0.5 ml/Patient received Moderna vaccine Booster on 04/08/2022) and EXPIRED PRODUCT ADMINISTERED (Vaccine was given beyond use date) in a 32-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. The patient had no known drug allergy. Acute illnesses at the time of vaccination and up to one month before was reported as none. Chronic or long-standing health conditions were reported as unknown. On 08-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 08-Apr-2022, the patient experienced ACCIDENTAL OVERDOSE (Dose/volume 0.5 ml/Patient received Moderna vaccine Booster on 04/08/2022) and EXPIRED PRODUCT ADMINISTERED (Vaccine was given beyond use date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was administered to patient 2 days past the 30-day time in refrigerator). At the time of the report, PRODUCT STORAGE ERROR (Vaccine was administered to patient 2 days past the 30-day time in refrigerator), ACCIDENTAL OVERDOSE (Dose/volume 0.5 ml/Patient received Moderna vaccine Booster on 04/08/2022) and EXPIRED PRODUCT ADMINISTERED (Vaccine was given beyond use date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered EXPIRED PRODUCT ADMINISTERED (Vaccine was given beyond use date) to be not related. No further causality assessments were provided for PRODUCT STORAGE ERROR (Vaccine was administered to patient 2 days past the 30-day time in refrigerator) and ACCIDENTAL OVERDOSE (Dose/volume 0.5 ml/Patient received Moderna vaccine Booster on 04/08/2022). Prescriptions, over-the-counter medications, dietary supplements, or herbal remedies being taken at time of vaccination and/or at the time of the adverse event was reported as unknown. The patient received Moderna vaccine booster on 08-Apr-2022. Vaccine was given beyond use date. Vaccine was received in refrigerator on 07-Mar-2022 in appropriate temperature (2-8 Celsius). Vaccine was administered to patient 2 days past the 30-day time in refrigerator. The vial did not undergo any temperature excursion. The event did not cause the patient to seek medical care. There were no any other potential causes. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental overdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: The patient had no known drug allergy. Acute illnesses at the time of vaccination and up to one month before was reported as none. Chronic or long-standing health conditions were reported as unknown.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 26.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was stored in refrigerator on 07-Mar-2022, dose administered after 30 days use by date on 11 -Apr-2022; Vaccine was stored in refrigerator on 07-Mar-2022, dose administered after 30 days use by date on 11 -Apr-2022; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was stored in refrigerator on 07-Mar-2022, dose administered after 30 days use by date on 11 -Apr-2022) and PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 07-Mar-2022, dose administered after 30 days use by date on 11 -Apr-2022) in a 32-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .5 milliliter. On 11-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was stored in refrigerator on 07-Mar-2022, dose administered after 30 days use by date on 11 -Apr-2022). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 07-Mar-2022, dose administered after 30 days use by date on 11 -Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was stored in refrigerator on 07-Mar-2022, dose administered after 30 days use by date on 11 -Apr-2022) and PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 07-Mar-2022, dose administered after 30 days use by date on 11 -Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered EXPIRED PRODUCT ADMINISTERED (Vaccine was stored in refrigerator on 07-Mar-2022, dose administered after 30 days use by date on 11 -Apr-2022) to be not related. No further causality assessment was provided for PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 07-Mar-2022, dose administered after 30 days use by date on 11 -Apr-2022). Concomitant product use was not provided by the reporter. Vaccine was received in refrigerator on 07-Mar-2022 in appropriate temperature (2-8 Celsius). Vaccine was administered to patient 5 days past the 30 day time in refrigerator. Vial did not undergo any temperature excursions. The patient received Moderna vaccine Booster on 11-Apr-2022. Vaccine was given beyond use date. The event did not cause the patient to seek medical care. There were no any other potential causes. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 3,0
- Dosis
- 4
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Joint range of motion decreased
Peripheral swelling
Symptomtext
Patient came in said her arm was red and swollen from shoulder to elbow joint. The arm was hard to raise and she couldn't extend it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 20.04.2022
- Beginn
- 20.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
The patient came and reported that she got Moderna vaccine in her country but could not get records of the immunizations because they would not give it to her. Her PCP recommended for her to restart series. Family wanted her to get Moderna vaccine. The patient was observed and had no complications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A.
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- No.
- Andere Medikamente
- No.
- Allergien
- No.
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 19.04.2022
- Impfdatum
- 22.01.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- 69,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint swelling
Nerve conduction studies normal
Neuropathy peripheral
Symptomtext
Joint swelling in hands and foreamrs - inflammatory - going through diagnosis procis through orthopedic, neurology, rheumatology. Steroid treatments in hands and forarms twice (repeat of inflamatioin after dimmunation for two months). No demylination as conduction studies normal but some periheral neuorpath in fine sensore in hands and forearms. Waiting for appointments on anothe orthopedic referral and rheumatology.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Joint swelling
- Hospital-Tage
- -
- Labordaten
- Initial orthopedic evaluation with steroid infections in all hand synovial tendon sheafs. mid 2021. Reports to urgenent care and referral to neurology and nephrology. End off 2021. Problems with appointments due to covid - just completed neurology end of March 2022. Waiting for orthopedic and rheumatology first two weeks in May 2022. Primary physician. Nowc. retiired. Due to covid I have been visiting for almost two years helping daughter and son in law with complications with covid including helping care for grandson with bilateral lip and palate. Have not seen primary doctor, just urgent care and speacilists. Early orthopedic suggestted surgery on one finger. However, had to leave for visit again before action.
- Aktuelle Erkrankungen
- Cataplexy (from 2009-2010 H1N1 variant - associated with a later viral infection). Loss of Hypocretin neurons in lateral nucleus in hypothalamus). Supporting reseach (originally thought to be related to GSK vaccine but later connected with actual viral generated antibody when it occurred in country who had not received vaccination - thought that approximately 30,000 people world wide afflicted and developed narcolepsy with or with out cataplexy. I only have sever cataplexy.
- Vorgeschichte
- Cataplexy, high blood pressure List of Moderna covid vaccines received First - Moderna 026L20A 01A 01/22/2021 Second Moerna 628L20A 02/22/2021 Third Moderna 088N21A 08/17/2021 (full dose for those with autoimmune) Fourth Moderna 046L21A Booster dose
- Andere Medikamente
- Prescriptions Drug Name/ AMLODIPINE 5MG TAB/ GABAPENTIN 300MG CAP/ LOSARTAN 100MG TAB/ PANTOPRAZOLE SOD 40MG TAB/ POTA CITRATE CR 1080MG TAB/ SPIRONOLACTONE 25MG TAB/ VENLAFAXINE ER 75MG CAP/ ZOLPIDEM 10MG TAB/ METFORMIN 500MG TAB E
- Allergien
- PNEUMOVAX TAPE (Paper ok) BENADRYL PROZAC (short term memory side effect) KEFLEX (Cephalexin) BENZOIN COMPOUND TALWIN ANTIHISTAMINES (Benadryl class - Hydroxyzine ok) TETRACYCLINE (hives) BISOPROLOL (BRONCHOSPASM) FLUOXETINE (Prozac)
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 19.04.2022
- Beginn
- 19.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient received her second booster too soon. She was due 5/27 and was given the vaccine 4/19. About 42 days early. No known adverse events. Patient was made aware of the error and was directed to the app as well to keep an eye on adverse events.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 18.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 2,0
- Dosis
- 4
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Audiogram abnormal
Magnetic resonance imaging head normal
Scan with contrast normal
Vertigo
Vestibular neuronitis
Symptomtext
2 days post vaccine I developed significant vertigo. Now, 4 days later, I have not improved. It does get better as the day goes on. Audiology test suggests a possible central cause or at least not Benign Paroxysmal Postural Vertigo. . MRI of the brain with contrast shows not central lesions. Working diagnosis is post vaccine vestibular neuritis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Audiogram abnormal
- Hospital-Tage
- -
- Labordaten
- Audiology test on 4/18/2022 MRI of brain with gadolinium-4/18/2022
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Crestor-40mg a day Prozac-40 mg a day
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 18.04.2022
- Impfdatum
- 18.04.2022
- Beginn
- 18.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Inappropriate schedule of product administration
Interchange of vaccine products
No adverse event
Symptomtext
The patient received Pfizer as the first dose on 3/23/2022. The patient was given Moderna as a second dose on 4/18/2022. No adverse reactions after Pfizer or Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- none
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.04.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
Patients were administered from vaccines that experienced a T excursion; Patients were administered from vaccines that experienced a T excursion; This spontaneous case was reported by an other health care professional and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Patients were administered from vaccines that experienced a T excursion) and POOR QUALITY PRODUCT ADMINISTERED (Patients were administered from vaccines that experienced a T excursion) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Patients were administered from vaccines that experienced a T excursion) and POOR QUALITY PRODUCT ADMINISTERED (Patients were administered from vaccines that experienced a T excursion). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Patients were administered from vaccines that experienced a T excursion) and POOR QUALITY PRODUCT ADMINISTERED (Patients were administered from vaccines that experienced a T excursion) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. HCP stated they had a temperature excursion and patients have been administered from these affected vaccines but did not have more information about the patients. The vaccines reached a Maximum temperature of 1.6 ?C for 1 hour and 12 min. Storage condition at the time of the excursion was refrigerated. Maximum or minimum temperatures reached, as applicable was Minimum 1.6 ?C on 24-Mar-2022. Excursion duration was Hour and 12 min. Date vial(s) moved from freezer to refrigerator was 13-Mar-2022. The vials were stored in refrigerator now. Number of vials/doses impacted was 4 vials. Pertinent details, whether the vial(s) were punctured, any previous excursions with the impacted vial(s) was unpunctured and no excursions before. No treatment information was provided. Most recent FOLLOW-UP information incorporated above includes: On 08-Apr-2022: Non-significant follow up information received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 79,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 12.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
The patient is immunocompromised received 0.5 ml as a second booster dose instead of 0.25 ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 14.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 11,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immunosuppression
Incorrect dose administered
Symptomtext
The patient is immunosuppressed and received the second booster but instead of receiving 0.25 ml the patient received 0.5 ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunosuppression
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- no known drug allergies
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 14.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immunodeficiency
Incorrect dose administered
Symptomtext
The Patient is immunocompromised and receive the second booster dose but instead of 0.25 ml the patient received 0.5 ml
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Immunodeficiency
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- -
- Allergien
- No known Drug Allergies
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 40,0
- Geschlecht
- U
- Eingang
- 13.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
VACCINE WAS GIVEN BEYOND USE DATE. VACCINE WAS RECEIVED IN REFRIGERATOR ON 03/07/2022 AND KEPT IN REFRIGERATOR IN APPROPRIATE TEMPERATURE (2-8 CELSIUS). VACCINE WAS GIVEN TO PATIENT 2 DAYS PAST THE 30 DAY TIME IN REFRIGERATOR
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 11.04.2022
- Beginn
- 11.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
VACCINE WAS GIVEN BEYOND USE DATE. VACCINE WAS RECEIVED IN REFRIGERATOR ON 03/07/2022 AND KEPT IN REFRIGERATOR IN APPROPRIATE TEMPERATURE (2-8 CELSIUS). VACCINE WAS GIVEN TO PATIENT 2 DAYS PAST THE 30 DAY TIME IN REFRIGERATOR
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS GIVEN BEYOND USE DATE. VACCINE WAS RECEIVED IN REFRIGERATOR ON 03/07/2022 AND KEPT IN REFRIGERATOR IN APPROPRIATE TEMPERATURE (2-8 CELSIUS). VACCINE WAS GIVEN TO PATIENT 2 DAYS PAST THE 30 DAY TIME IN REFRIGERATOR
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- UNKNOWN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS GIVEN BEYOND USE DATE. VACCINE WAS RECEIVED IN REFRIGERATOR ON 03/07/2022 AND KEPT IN REFRIGERATOR IN APPROPRIATE TEMPERATURE (2-8 CELSIUS). VACCINE WAS GIVEN TO PATIENT 2 DAYS PAST THE 30 DAY TIME IN REFRIGERATOR
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS GIVEN BEYOND USE DATE. VACCINE WAS RECEIVED IN REFRIGERATOR ON 03/07/2022 AND KEPT IN REFRIGERATOR IN APPROPRIATE TEMPERATURE (2-8 CELSIUS). VACCINE WAS GIVEN TO PATIENT 2 DAYS PAST THE 30 DAY TIME IN REFRIGERATOR.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
VACCINE WAS GIVEN BEYOND USE DATE. VACCINE WAS RECEIVED IN REFRIGERATOR ON 03/07/2022 AND KEPT IN REFRIGERATOR IN APPROPRIATE TEMPERATURE (2-8 CELSIUS). VACCINE WAS GIVEN TO PATIENT 2 DAYS PAST THE 30 DAY TIME IN REFRIGERATOR
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 13.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS GIVEN BEYOND USE DATE. VACCINE WAS RECEIVED IN REFRIGERATOR ON 03/07/2022 AND KEPT IN REFRIGERATOR IN APPROPRIATE TEMPERATURE (2-8 CELSIUS). VACCINE WAS GIVEN TO PATIENT 2 DAYS PAST THE 30 DAY TIME IN REFRIGERATOR
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- NOT KNOWN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
VACCINE WAS GIVEN BEYOND USE DATE. VACCINE WAS RECEIVED IN REFRIGERATOR ON 03/07/2022 AND KEPT IN REFRIGERATOR IN APPROPRIATE TEMPERATURE (2-8 CELSIUS). VACCINE WAS GIVEN TO PATIENT 2 DAYS PAST THE 30 DAY TIME IN REFRIGERATOR.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- UNKNOWN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 13.04.2022
- Impfdatum
- 08.04.2022
- Beginn
- 08.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Expired product administered
Symptomtext
VACCINE WAS GIVEN BEYOND USE DATE. VACCINE WAS RECEIVED IN REFRIGERATOR ON 03/07/2022 AND KEPT IN REFRIGERATOR IN APPROPRIATE TEMPERATURE (2-8 CELSIUS). VACCINE WAS GIVEN TO PATIENT 2 DAYS PAST THE 30 DAY TIME IN REFRIGERATOR
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- NOT KNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- NOT KNOWN
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Product storage error
Symptomtext
GAVE PATIENT MODERNA 4TH DOSE FROM EXPIRED VIAL.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- 2/10/2019 Left total hip arthroplasty (COMPLETED) 01/26/2018 transrectal ultrasound (COMPLETED) prostate needle biopsy --------------------------- DX - Outpt Problem List --------------------------- Date Facility Hospital Location Encounter Elig. 04/12/22 INTERNAL MEDICINE SC LESS THAN 50% Provider: Diagnosis: Invalid coding system specified-; Encounter for Immunization (P) **MOST RECENT EPISODE OF THIS DIAGNOSIS** 03/09/22 ORTHO/JOINT SURG SC LESS THAN 50% Provider: Diagnosis: Invalid coding system specified-; Presence of left Artificial Hip Joint (P) **MOST RECENT EPISODE OF THIS DIAGNOSIS** 01/25/22 PRIMARY CARE/MEDICINE SC LESS THAN 50% Provider: MD Diagnosis: Invalid coding system specified-; Prostate cancer (SCT) (P) **MOST RECENT EPISODE OF THIS DIAGNOSIS** Invalid coding system specified-; History of male erectile disorder (SCT) **MOST RECENT EPISODE OF THIS DIAGNOSIS** Invalid coding system specified-; Acquired hypothyroidism (SCT) **MOST RECENT EPISODE OF THIS DIAGNOSIS** Invalid coding system specified-; Hyperlipidemia (SCT) **MOST RECENT EPISODE OF THIS DIAGNOSIS** 06/29/21 NEUROLOGY SC LESS THAN 50% Provider: Diagnosis: Invalid coding system specified-; Dysphagia (SCT) (P) **MOST RECENT EPISODE OF THIS DIAGNOSIS** 05/11/21 TELEPHONE/MEDICINE SC LESS THAN 50% Provider: Diagnosis: Invalid coding system specified-; Other specified Counseling (P) **MOST RECENT EPISODE OF THIS DIAGNOSIS** 04/01/21 GI ENDOSCOPY SC LESS THAN 50% Provider: Diagnosis: Invalid coding system specified-; Other Diseases of Stomach and Duodenum Invalid coding system specified-; Gastro-Esophageal Reflux Disease without Esophagitis 03/30/21 PRIMARY CARE/MEDICINE SC LESS THAN 50% Provider: Diagnosis: Invalid coding system specified-; Contact with and (suspected) exposure to COVID-19 (P) 02/11/21 SPEECH-LANGUAGE PATHOLOGY SC LESS THAN 50% Provider: Diagnosis: Invalid coding system specified-; Dysphagia, Oropharyngeal Phase (P) **MOST RECENT EPISODE OF THIS DIAGNOSIS** 01/25/21 PRIMARY CARE SC LESS THAN 50% Provider: Diagnosis: Invalid coding system specified-; Leukopenia (SCT) **MOST RECENT EPISODE OF THIS DIAGNOSIS** Invalid coding system specified-; Unexplained weight loss (CT) 01/22/21 OPHTHALMOLOGY SC LESS THAN 50% Provider: Diagnosis: Invalid coding system specified-; Encounter for Examination of Eyes and Vision with Abnormal Findings (P) 01/22/21 OPHTHALMOLOGY SC LESS THAN 50% Provider: Diagnosis: Invalid coding system specified-; Encounter for Examination of Eyes and Vision without Abnormal Findings (P) 10/05/20 PRIMARY CARE/MEDICINE SC LESS THAN 50% Provider: Diagnosis: Invalid coding system specified-; Encounter for Screening, unspecified (P) **MOST RECENT EPISODE OF THIS DIAGNOSIS** 03/30/20 PRIMARY CARE SC LESS THAN 50% Provider: Diagnosis: Invalid coding system specified-; Anemia (SCT) **MOST RECENT EPISODE OF THIS DIAGNOSIS** 01/23/20 ORTHO/JOINT SURG SERVICE CONNECTED Provider: Diagnosis: Invalid coding system specified-; Pain in left Hip (P) **MOST RECENT EPISODE OF THIS DIAGNOSIS** 01/09/20 KINESIOTHERAPY SERVICE CONNECTED Provider: Diagnosis: Invalid coding system specified-; Osteoarthritis of hip (SCT) (P) **MOST RECENT EPISODE OF THIS DIAGNOSIS** 12/19/19 EMERGENCY DEPT SERVICE CONNECTED Provider: Diagnosis: Invalid coding system specified-; Pt Leaving Prior to Being Seen by Provider (P) 12/13/19 OCCUPATIONAL THERAPY SERVICE CONNECTED Provider: Diagnosis: Invalid coding system specified-; Encounter for other specified Aftercare (P) **MOST RECENT EPISODE OF THIS DIAGNOSIS** 12/10/19 PATIENT CARE SERVICE CONNECTED Provider: Diagnosis: Invalid coding system specified-; Encounter for other Preprocedural Examination (P) **MOST RECENT EPISODE OF THIS DIAGNOSIS**
- Andere Medikamente
- 1) ATORVASTATIN CALCIUM 10MG TAB TAKE ONE TABLET BY ACTIVE MOUTH AT BEDTIME FOR HIGH CHOLESTEROL 2) LEVOTHYROXINE NA (SYNTHROID) 150MCG TAB TAKE ONE ACTIVE TABLET BY MOUTH EVERY MORNING FOR THYROID (TAKE ON
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 12.04.2022
- Impfdatum
- 05.04.2022
- Beginn
- 05.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
No adverse event
Symptomtext
NO ADVERSE REACTION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- KNEE CONDITION 10% SC LIMITED MOTION OF ANKLE 0% SC 2ND DEGREE BURNS 0% SC PARALYSIS OF SCIATIC NERVE 10% SC HYPERTENSIVE VASCULAR DISEASE 0% SC SCARS 0% SC PARALYSIS OF SCIATIC NERVE 10% SC ARTHRITIS, DEGENERATIVE 0% SC SLEEP APNEA SYNDROMES 50% SC LIMITED MOTION OF ARM 0% SC DEGENERATIVE ARTHRITIS OF THE SPINE 10% SC
- Andere Medikamente
- ) ACCU-CHEK GUIDE (GLUCOSE) TEST STRIP USE 1 STRIP FOR ACTIVE TESTING (MEDICAL SUPPLY) AS DIRECTED 2) ALOGLIPTIN 25MG TAB TAKE ONE TABLET BY MOUTH EVERY ACTIVE DAY FOR DIABETES, MAY BE TAKEN WITHOUT REGARD TO
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 09.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 07.04.2022
- Beginn
- 07.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 5
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Inappropriate schedule of product administration
No adverse event
Symptomtext
No adverse reaction. 2nd booster dose administered 2 weeks early. Patient did not have actual CDC vaccination card, presented Docket app, with three dates of Moderna vaccines, 1/6/2021, 2/2/2021, and 8/18/2021. With the information presented the patient received a booster dose of Moderna 0,25 mL. Later when documenting the dose it was noted that the patient had received a dose of Pfizer vaccine on 12/21/2021 and the three full doses noted for a primary series of three and the Pfizer being her first booster. In a follow-up call to patient she stated "I forgot I received a booster in December".
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- RA
- Andere Medikamente
- Unknown
- Allergien
- No known allergies.
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Incorrect dose administered
No adverse event
Symptomtext
patient received 0.5ml instead of 0.25ml dose. No adverse affects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Incorrect dose administered
No adverse event
Symptomtext
patient recevied 0.5ml instead of 0.25ml dose. No adverse affects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 94,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Incorrect dose administered
No adverse event
Symptomtext
Patient recevied 0.5ml dose instead of 0.25ml dose. No adverse affects per patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
Patient recevied 0.5ml instead of 0.25ml dose. No adverse affects per patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
patient recevied 0.5ml instead of 0.25ml. No adverse affects per patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 03.04.2022
- Tage bis Beginn
- 1,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Contusion
Symptomtext
Bruising of right arm from shoulder down to wrist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Contusion
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/a
- Allergien
- N/a
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vaccine was stored in the refrigerator 03-Mar-2022 and administered on 04-Apr-2022; Patient received expired vaccine, beyond 30-day Use By Date; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient received expired vaccine, beyond 30-day Use By Date) and PRODUCT STORAGE ERROR (The vaccine was stored in the refrigerator 03-Mar-2022 and administered on 04-Apr-2022) in a 33-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 04-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient received expired vaccine, beyond 30-day Use By Date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vaccine was stored in the refrigerator 03-Mar-2022 and administered on 04-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient received expired vaccine, beyond 30-day Use By Date) and PRODUCT STORAGE ERROR (The vaccine was stored in the refrigerator 03-Mar-2022 and administered on 04-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not provided. The vaccines placed in refrigerator on 03-Mar-2022, and doses administered to patient after 30-day use by date on 04-Apr-2022 around 9AM . The patient received first booster dose. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Incorrect dose administered
Symptomtext
Patient received 1st dose of Moderna in October. Instead of giving the patient a second dose (0.5 mL) of Moderna, I accidentally gave 0.25 mL (booster dose) assuming it was a booster shot since it was far out from his first dose. Patient was alerted and notified.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- No
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 05.04.2022
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
On 3/21/22 Patient was administered covid vaccine booster after he stated that he had not received any prior booster and providing different year of birthdate. He was administered booster dose of moderna. Patient stated no hx of allergies, health risks, or being immunocompromised. After 15 minutes of being monitored he left clinic, and stated feeling well; no adverse effect reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Leakage occurred between needle and syringe upon administration. Patient notified. CDC errors document reviewed, booster dose re-administered per CDC guidance. Patient in agreement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 04.04.2022
- Impfdatum
- 04.04.2022
- Beginn
- 04.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Patient was given a 0.25 ml Moderna booster today (4/4/22 )around 9am which had a refrigerator expiration date of 4/3/22 (yesterday). No adverse reaction reported by patient. The vaccine was pulled from the freezer on 3/3/22 with a manufacturer expiration date of 7/6/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- bilateral low back pain
- Andere Medikamente
- n/a
- Allergien
- sulfonamide antibiotics
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 02.04.2022
- Impfdatum
- 02.04.2022
- Beginn
- 02.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Tinnitus
Symptomtext
Tinnitus - Right ear
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoarthritis Osteoporosis
- Andere Medikamente
- Raloxifene/Evista Vitamins Lysine
- Allergien
- Non-celiac gluten sensitivity Aspirin Chondroitin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 31.03.2022
- Beginn
- 31.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Symptomtext
Patient received a second booster (Moderna) outside the CDC guidelines as she was 37 years old and not immunocompromised. She had received Janssen as her primary series and already received an mRNA booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- na
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 96,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- Impfdatum
- 07.02.2022
- Beginn
- 28.02.2022
- Tage bis Beginn
- 21,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Aortic aneurysm
Symptomtext
Hospital admission for abdominal aortic Aneurysm. Patient transferred to hospice. Hospital admission within 6 weeks of receiving the COVIDD vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Aortic aneurysm
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product contamination physical
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product contamination physical
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product contamination physical
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product contamination physical
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product contamination physical
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- U
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product contamination physical
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product contamination physical
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product contamination physical
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 29.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product contamination physical
Symptomtext
At the end of the clinic, healthcare staff noticed a gray particle inside of the Moderna vial. It is unsure whether it is part of the rubber stopper or if it is a foreign material. After monitoring the patient for over 15 minutes, there were no adverse signs or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product contamination physical
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 02.02.2022
- Beginn
- 02.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
No adverse event
Symptomtext
2nd dose of Moderna vaccine was given at 3 weeks instead of four weeks . Patient denied any adverse reactions
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 30.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 25.03.2022
- Tage bis Beginn
- 24,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Interchange of vaccine products
Symptomtext
'Patient mistakenly given 0.5 ml dose of Moderna Covid vaccine approx 1 year after rcv'ng J&J Covid vaccine, as a second dose instead of 0.25 ml dose as a booster (as variously mandated by CDC and FDA per current guidelines).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 24.03.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Delivery
Exposure during pregnancy
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Date of delivery 7/30/2022. Patient did not have adverse event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Delivery
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Aspirin 81 mg; Zofran 4 mg
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 23.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Underdose
Symptomtext
no adverse event pt just received 2 full doses and 2 boosters instead of 3 full and one booster like she was eligible for
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- thyroid cancer depression copd
- Andere Medikamente
- methimazole amlodipine paxil Lipitor Trintellix anoro ellipta
- Allergien
- ivp dye
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Pt was given Moderna as her 2nd dose in her primary series when Pfizer was her 1st dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Menstruation delayed
Symptomtext
My period is almost a week late with no signs of making an appearance. After receiving the first 2 COVID shots my periods were different too. They were heavier, but still came on time each month. Please acknowledge the fact that these vaccines have an effect on a woman's cycle.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Menstruation delayed
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COVID-19 30 days prior
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 21.03.2022
- Impfdatum
- 21.03.2022
- Beginn
- 21.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Exposure during pregnancy
Product administered to patient of inappropriate age
Symptomtext
Patient is pregnant, 23w 4d, due on July 14, 2022. The patient was given Moderna in error this morning as she is only 15 years old. This was her first Covid vaccination. She tolerated the vaccine fine and had no other issues other than receiving Moderna instead of Pfizer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exposure during pregnancy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- teenage pregnancy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Interchange of vaccine products
Symptomtext
Gave .50ml dose (should have had .25ml dose as booster to J&J)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 18.03.2022
- Beginn
- 18.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Given .50ml dose Vaccine (should have given .25ml as it was a booster to J&J)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- Impfdatum
- 17.02.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pulmonary congestion
Upper respiratory tract congestion
Symptomtext
Upper respiratory and lung congestion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary congestion
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Maternal exposure during pregnancy
Product administered to patient of inappropriate age
Symptomtext
15 y/o pregnant female at OB Intake given Moderna Booster dose. Previous covid vaccines had been Pfizer Purple Cap. Pt is approx 8.6 weeks pregnant with history of nausea and vomiting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 18.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- 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
Product storage error
Symptomtext
Vial was initially stored in refrigerator on 08-Feb-2022 and administered on 15-Mar-2022; Patient was administered Moderna COVID-19 dose after the 30 days use by date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient was administered Moderna COVID-19 dose after the 30 days use by date) and PRODUCT STORAGE ERROR (Vial was initially stored in refrigerator on 08-Feb-2022 and administered on 15-Mar-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 15-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient was administered Moderna COVID-19 dose after the 30 days use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was initially stored in refrigerator on 08-Feb-2022 and administered on 15-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient was administered Moderna COVID-19 dose after the 30 days use by date) and PRODUCT STORAGE ERROR (Vial was initially stored in refrigerator on 08-Feb-2022 and administered on 15-Mar-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication was reported. It was reported that, the vial was initially stored in the refrigerator on 08-Feb-2022 and vial did not undergo any temperature excursions. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- -
- Geschlecht
- U
- Eingang
- 18.03.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- 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
Product storage error
Symptomtext
Vial was initially stored in refrigerator on 08-Feb-2022 and administered on 10-Mar-2022; Administered COVID-19 dose after the 30 days use by date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Administered COVID-19 dose after the 30 days use by date) and PRODUCT STORAGE ERROR (Vial was initially stored in refrigerator on 08-Feb-2022 and administered on 10-Mar-2022) in a patient of an unknown age and gender who received mRNA-1273 (Spikevax) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Mar-2022, the patient received dose of mRNA-1273 (Spikevax) (Intramuscular) 1 dosage form. On 10-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Administered COVID-19 dose after the 30 days use by date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was initially stored in refrigerator on 08-Feb-2022 and administered on 10-Mar-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Administered COVID-19 dose after the 30 days use by date) and PRODUCT STORAGE ERROR (Vial was initially stored in refrigerator on 08-Feb-2022 and administered on 10-Mar-2022) outcome was unknown. For mRNA-1273 (Spikevax) (Intramuscular), the reporter did not provide any causality assessments. Vial was initially stored in refrigerator on 08-Feb-2022. Vial did not undergo any temperature excursion. No concomitant medication was reported by reporter. No treatment medication was reported by reporter. This case was linked to MOD-2022-512525, MOD-2022-512526 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 16.03.2022
- Impfdatum
- 15.03.2022
- Beginn
- 15.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Error: Wrong Vaccine Formulation (ex. different manufact. initial and booster)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.03.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
The vial was initially stored in the refrigerator on 07 Feb 2022 and date of administration of vaccine was on 10 Mar 2022; A single dose of Moderna Covid-19 vaccine was given to a patient on the 31st day in the refrigerator. This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (A single dose of Moderna Covid-19 vaccine was given to a patient on the 31st day in the refrigerator.) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 07 Feb 2022 and date of administration of vaccine was on 10 Mar 2022) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Mar-2022 at 5:00 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 10-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (A single dose of Moderna Covid-19 vaccine was given to a patient on the 31st day in the refrigerator.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 07 Feb 2022 and date of administration of vaccine was on 10 Mar 2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (A single dose of Moderna Covid-19 vaccine was given to a patient on the 31st day in the refrigerator.) and PRODUCT STORAGE ERROR (The vial was initially stored in the refrigerator on 07 Feb 2022 and date of administration of vaccine was on 10 Mar 2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications was not provided by the reporter. A single dose of Moderna Covid-19 vaccine was given to a patient on the 31st day in the refrigerator. Date the vial was initially stored in the refrigerator on 07 Feb 2022 at 10:31am. The vial did not undergo any temperature excursion. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 15.03.2022
- Impfdatum
- 10.03.2022
- Beginn
- 10.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product storage error
Symptomtext
Expired/deteriorated vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 11.03.2022
- Impfdatum
- 11.03.2022
- Beginn
- 11.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient received his booster shot approximately three months too soon. His Moderna series (1&2) was completed on 01/07/2022, and he received his booster on 03/11/2022. He is not immunocompromised, or otherwise eligible for earlier dosing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- DC
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 16.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine was left out in room temperature post-punctured over 12 hours and "one" patient received booster; Vaccine was left out in room temperature post-punctured over 12 hours and one patient received booster; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vaccine was left out in room temperature post-punctured over 12 hours and one patient received booster) and PRODUCT STORAGE ERROR (Vaccine was left out in room temperature post-punctured over 12 hours and "one" patient received booster) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Mar-2022 at 2:56 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Mar-2022 at 2:56 PM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vaccine was left out in room temperature post-punctured over 12 hours and one patient received booster). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was left out in room temperature post-punctured over 12 hours and "one" patient received booster). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vaccine was left out in room temperature post-punctured over 12 hours and one patient received booster) and PRODUCT STORAGE ERROR (Vaccine was left out in room temperature post-punctured over 12 hours and "one" patient received booster) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant drugs were not reported. Treatment details were not given. Vial was first punctured on 07-Mar-2022 around 9:00 AM . It did not undergo any temperature excursions. Most recent FOLLOW-UP information incorporated above includes: On 09-Mar-2022: Follow up received contains significant information- As involved patient number updated from two to one.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Received expired vaccine 12 hours post puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired vaccine 12 hours post puncture) in an adult patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired vaccine 12 hours post puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received expired vaccine 12 hours post puncture) 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. The pharmacist was calling to report that two patients in their 30's received expired booster of Moderna. The dose was administered >12 post puncture. The date the vial was initially stored in the refrigerator was 03-Mar-2022. The date and time the vial first punctured was 07-Mar-2022 at 5PM. The date and time of administration of vaccine was on 08-Mar-2022 at 12:45PM and 1:17PM. The vial was stored in room temperature post puncture. Reportedly, the vial didn't undergo any temperature excursions. The total amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) was about 20 hours. It was also reported that the vial was not exposed to room temperature for more than 24 hours. No treatment information was provided. This case was linked to MOD-2022-505347 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- -
- Geschlecht
- U
- Eingang
- 11.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Received expired vaccine greater than 12 hours post puncture; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Received expired vaccine greater than 12 hours post puncture) in an adult patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 08-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 08-Mar-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Received expired vaccine greater than 12 hours post puncture). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Received expired vaccine greater than 12 hours post puncture) 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. Patient in their 30's received vaccine which is initially stored in refrigerator on 03-Mar-2022, on 07-Mar-2022 at 05:00 PM vial was initially punctured and stored in room temperature range (8 degree to 25 degree C, 46 degree to 77 degree F) for about 20 hours, on 08-Mar-2022 two patients got vaccinated at 12:45PM and 01:17PM. It mentioned that the vial did not undergo any temperature excursions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 09.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Laboratory test
Lip swelling
Swollen tongue
Symptomtext
Woke up Tuesday morning with my bottom lip swelling. Took Benadryl around 1pm, as the swelling continued. Around 3pm, my tongue started swelling and I went to the Er
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Laboratory test
- Hospital-Tage
- -
- Labordaten
- All recorded at Hospital
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 09.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 09.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 08.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
The patient was given expired moderna. The medication expired approximately 8 hours and 17 minutes upon administration. No adverse effect so far
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 08.03.2022
- Beginn
- 08.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
The patient was given an expired moderna. Moderna was expired approximately 7 hours and 15 minutes before administration. no adverse effect yet
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none so far
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- omeprazole, gabapentin, celecoxib, prochlorperazine, phentermine
- Allergien
- none but gets unknown allergic rash so carries around epi-pen
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
The patient received a booster dose of Moderna instead of the Pfizer second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Schizophrenia Diabetes HTN Hypothyroidism
- Andere Medikamente
- Risperidone, Divalproex, Fluoxetine, Benztropine, Synthroid, Furosemide, Simvastatin, Metformin
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 08.03.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
Symptomtext
The patient received a booster dose of Moderna vaccine instead of a Pfizer second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Artritis
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 07.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
No adverse event
Symptomtext
Booster dose was administered to resident prior to the recommended interval, no adverse effect noted, no unusual changes. Resident made aware that booster dose was administered prior to the recommended interval. Resident made aware of possible adverse reaction post vaccine, to inform Nurses if any change of condition occurs and verbalized understanding. MD aware with order to monitor resident for any possible adverse effect.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- no adverse effect noted to resident, no test done
- Aktuelle Erkrankungen
- DM2 HTN BPH Atherosclerotic Heart Disease Acute Kidney Failura
- Vorgeschichte
- -
- Andere Medikamente
- n/a
- Allergien
- ACE inhibitors
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 04.03.2022
- Impfdatum
- 04.03.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient came to the pharmacy to get a COVID vaccine. When asked the patient for their vaccine card, they stated that it was their first shot and that they have never had one before. Patient asked about the difference between the two vaccines (moderna and pfizer) and requested to get Moderna. Before administering the 0.5 mL of the Moderna, I asked the patient again if this is their first COVID vaccine and they said "yes, I have never had one before." I gave the patient the vaccine and had them wait for 15 minutes to make sure there was no reaction. After the vaccine was administered, it was discovered that the patient has had the Pfizer vaccine 1st and 2nd dose last February and the booster in September. Patient never verbally disclosed this information upon checking in or prior to receiving the vaccine even though they were asked several times. I called the patient and let them know to not get anymore doses of the COVID vaccine until further guidelines are established by the CDC.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- No tests or labs were done.
- Aktuelle Erkrankungen
- None listed
- Vorgeschichte
- None listed
- Andere Medikamente
- None listed
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 02.03.2022
- Impfdatum
- 01.03.2022
- Beginn
- 01.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
No Adverse events reported. Moderna administered in place of pfizer per patient representative (Father) wish. Got signed of by the pharmacist at the time
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- -
- Geschlecht
- U
- Eingang
- 01.03.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
booster dose administered out of vial punctured more than 12 hours; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (booster dose administered out of vial punctured more than 12 hours) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 25-Feb-2022 at 1:10 PM, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (booster dose administered out of vial punctured more than 12 hours). At the time of the report, EXPIRED PRODUCT ADMINISTERED (booster dose administered out of vial punctured more than 12 hours) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications details were not reported by the reporter. Reporter Stated that, the vials were stored at room temperature post puncture and the vials 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 are about 20 hours and 40 minutes. Treatment details was not reported by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Moderna booster give to 14 yr old pt . Moderna not authorized in this patients age group.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 27.02.2022
- Impfdatum
- 27.02.2022
- Beginn
- 27.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Product administered to patient of inappropriate age
Symptomtext
NO ADVERSE EVENTS, PATIENT HAD 2 DOSES OF PFIZER, MD WANTED HER TO CHANGE TO MODERNA, THEN REALIZED AFTER THE FACT THAT PATIENT IS 15
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 25.02.2022
- Impfdatum
- 25.02.2022
- Beginn
- 25.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Moderna Vial punctured on 02/24/2022 @ 4:30pm Administered booster dose to patient on 02/25/2022 @ 1:10pm Vial was left out in room temp from time of initial puncture to administration time of booster dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 8,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 23.02.2022
- Beginn
- 23.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- SC
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 21.02.2022
- Beginn
- 21.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Error: Wrong Dose of Vaccine - Too High-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 21.02.2022
- Impfdatum
- 19.02.2022
- Beginn
- 19.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Patient was inadvertently given booster (dose #3) of Moderna too early. Dose #2 was given 10/19/21 and dose #3 was given 2/19/22, which is early than the recommended 5-month interval.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 18.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Accidental underdose
Needle issue
Symptomtext
patient only received 75% of first dose; Needle twisted off of the syringe while adminstrating; This spontaneous case was reported by an other health care professional and describes the occurrence of ACCIDENTAL UNDERDOSE (patient only received 75% of first dose) and NEEDLE ISSUE (Needle twisted off of the syringe while adminstrating) in a 26-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. Concomitant products included CODEINE and AMOXICILLIN for an unknown indication. On 15-Feb-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Feb-2022, the patient experienced ACCIDENTAL UNDERDOSE (patient only received 75% of first dose) and NEEDLE ISSUE (Needle twisted off of the syringe while adminstrating). At the time of the report, ACCIDENTAL UNDERDOSE (patient only received 75% of first dose) and NEEDLE ISSUE (Needle twisted off of the syringe while adminstrating) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Reporter stated that patient got administered with first dose of Moderna COVID-19 vaccine on 15-Feb-2022 where there was only 75 percent of the dose went into the patient due to the needle twisting out of the syringe. Patient was okay. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Accidental underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- CODEINE; AMOXICILLIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 17.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
patient received o.5 ml's instead of 0.25 ml's for 4th dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- non
- Vorgeschichte
- hypertension, high cholesterol, crohns disease
- Andere Medikamente
- lisinopril, hydrochlorothiazide, atorvastatin, remicade infusions
- Allergien
- sulfa
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 17.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Symptomtext
Patient was given 0.5 ml's instead of 0.25 ml's for 4th dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- type 2 diabetes, high cholesterol, hypertension, cancer pain
- Andere Medikamente
- metformin, lovastatin, irbesartan, bicalutamide, tramadol, vegetable extract pill
- Allergien
- no known allergies
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 15,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 16.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
PATIENT GIVEN MODERNA VACCINE WHEN UNDER AGE OF 18 - NO REACTION AS OF 3 HOURS POST VACCINATION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Dispensed two doses of Moderna vaccine past 24 hours after vials removed from refrigerator; Dispensed two doses of a Moderna covid vaccine past it's storage and handling requirements; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dispensed two doses of Moderna vaccine past 24 hours after vials removed from refrigerator) and PRODUCT STORAGE ERROR (Dispensed two doses of a Moderna covid vaccine past it's storage and handling requirements) in a 42-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dispensed two doses of Moderna vaccine past 24 hours after vials removed from refrigerator) and PRODUCT STORAGE ERROR (Dispensed two doses of a Moderna covid vaccine past it's storage and handling requirements). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dispensed two doses of Moderna vaccine past 24 hours after vials removed from refrigerator) and PRODUCT STORAGE ERROR (Dispensed two doses of a Moderna covid vaccine past it's storage and handling requirements) 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. The reporter stated that they found out that they dispensed two doses of a Moderna Covid vaccine past its storage and handling requirements. The reporter informed that it has been greater than 24 hours after the vials had been removed from the refrigerator. Reportedly, the date the vial was initially stored in the refrigerator was 08-Feb-2022 and was removed from the fridge on 09-Feb-2022. The vaccine was administered on 10-Feb-2022. It was also reported that the vial didn't undergo any temperature excursions. The total amount of time the vial was exposed to room temperature range (8? to 25?C= 46? to 77?F) was 24-48 hours. No treatment information was provided. Most recent FOLLOW-UP information incorporated above includes: On 11-Feb-2022: Follow-up received contains no new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 16.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
dispensed two doses of Moderna vaccine past 24 hours after vials removed from refrigerator; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (dispensed two doses of Moderna vaccine past 24 hours after vials removed from refrigerator) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 046L21A) for COVID-19 vaccination. No Medical History information was reported. On 10-Feb-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 10-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (dispensed two doses of Moderna vaccine past 24 hours after vials removed from refrigerator). At the time of the report, EXPIRED PRODUCT ADMINISTERED (dispensed two doses of Moderna vaccine past 24 hours after vials removed from refrigerator) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications was not reported. Reported Total amount of time the vial was exposed to room temperature range (8 degree to 25 degree C= 46 degree to 77 degree F) and 24-48 hours. Reported Date the vial was initially stored in the refrigerator was 08FEB2022 Removed from the fridge on 09FEB2022 Treatment medications was not reported. Most recent FOLLOW-UP information incorporated above includes: On 11-Feb-2022: Follow up received includes non significant information
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Patient did not have any side affects or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 15.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
Patient did not have any side affects or symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NH
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
injected with an expired Moderna vial
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 05.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient is under 18 (age 17) and received Moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 12,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
There was no adverse events, the patient received the wrong vaccination for his age group. Pfizer is the only approved Covid-19 Vaccination for 12 year olds at this time.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Error: Patient Too Young for Vaccine Administered-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- ID / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Symptomtext
No adverse reaction apparent No treatment
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none reported
- Vorherige Impfungen
- -