- Staat
- MA
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 01.11.2023
- Impfdatum
- 19.03.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 292,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Cerebrovascular accident
Computerised tomogram
Disturbance in attention
Echocardiogram
Headache
Hemiparesis
Hypoaesthesia
Laboratory test
Magnetic resonance imaging
Scan myocardial perfusion
Symptomtext
Had numbness weakness on the entire right side head to toe. Head aches , could not concentrate on anything.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 5,0
- Labordaten
- Ct , mri 3/8/2022, echo, nuclear stress test. 3/4/2022 a Labs same day 3/4/2022.
- Aktuelle Erkrankungen
- High blood pressure
- Vorgeschichte
- None at the time of vaccinations. After vaccinations I had a stroke.
- Andere Medikamente
- Losartan 25mg
- Allergien
- Bactrim / cipro
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 06.04.2023
- Impfdatum
- 24.01.2022
- Beginn
- 29.12.2022
- Tage bis Beginn
- 339,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Asthenia
COVID-19
COVID-19 pneumonia
Condition aggravated
Fall
SARS-CoV-2 test positive
Symptomtext
Patient with history of COPD and dementia. He was brought to the ED by EMS on 12/29/22 for evaluation after a fall at home. His wife noted he has been more weak than normal. COVID PCR test performed in the ED resulted positive. He was admitted to the hospital 12/29/22 - 1/9/23. Discharge diagnoses included acute hypoxic respiratory failure due to COVID-19 pneumonia, among other diagnoses. Patient was on 2L O2 and was able to be weaned off to room air during his admission. Patient has received the primary COVID vaccine series and one booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 31.03.2023
- Impfdatum
- 01.03.2022
- Beginn
- 27.09.2022
- Tage bis Beginn
- 210,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cerebrovascular accident
SARS-CoV-2 test
Symptomtext
she had symptoms of Stroke; diagnosed her with Positive COVID Test; This spontaneous case was reported by a patient and describes the occurrence of CEREBROVASCULAR ACCIDENT (she had symptoms of Stroke) and COVID-19 (diagnosed her with Positive COVID Test) in a 74-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J21-2A) for COVID-19 prophylaxis. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for an unknown indication. Previously administered products included for Product used for unknown indication: J & J Covid-19 vaccine (First shot) on 09-Mar-2021 and Pfizer monovalent booster (2nd Pfizer monovalent booster) on 02-Nov-2021. Past adverse reactions to the above products included No adverse event with J & J Covid-19 vaccine and Pfizer monovalent booster. Concurrent medical conditions included Immunocompromised. On 01-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Sep-2022, the patient received fourth dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On 27-Sep-2022, the patient experienced CEREBROVASCULAR ACCIDENT (she had symptoms of Stroke) (seriousness criteria hospitalization and medically significant) and COVID-19 (diagnosed her with Positive COVID Test) (seriousness criterion hospitalization). At the time of the report, CEREBROVASCULAR ACCIDENT (she had symptoms of Stroke) and COVID-19 (diagnosed her with Positive COVID Test) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 27-Sep-2022, SARS-CoV-2 test: Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. Patient had symptoms of Stroke and went to the hospital, while patient was in the hospital, they diagnosed her with Positive COVID Test. No treatment information was reported. Company comment. This spontaneous case concerns a 74 ? year ? old female patient, with medical history of Immunodeficiency, who experienced the unexpected, serious (medically significant and hospitalization) AESI Cerebrovascular accident and the unexpected, serious (hospitalization) event of COVID ? 19. The events occurred approximately 7 months after a dose of mRNA ? 1273 original vaccine, reported as a booster dose of her COVID ? 19 immunization schedules; the patient previously had one dose of Janssen COVID ? 19 vaccines and one dose of Tozinameran COVID ? 19 vaccines. The report stated that the patient had symptoms of stroke and went to hospital. While she was in hospital, she was diagnosed with a positive COVID test. Twenty days prior the onset of the events the patient received an Omicron Booster dose with Tozinameran COVID ? 19 vaccine. No further clinical details were provided for medical reviewing. Patient?s mentioned medical history could be confounder for serious illness from COVID ? 19. Patient?s age and COVID ? 19 could be risk factors for cerebrovascular accident. Co ? suspect product Tozinameran COVID ? 19 vaccine remains as confounder. The benefit-risk relationship of mRNA ? 1273 original vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220927; Test Name: COVID Test; Test Result: Positive
- Aktuelle Erkrankungen
- Immunocompromised
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 13.09.2022
- Impfdatum
- 11.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cerebrovascular accident
Symptomtext
PER PATIENT'S WIFE: PATIENT HAD A STROKE AND NEEDED TO HOSPITALIZED
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- HIGH BLOOD PRESSURE, CHOLESTEROL, DIABETES, VITAMIN DEFICIENCY
- Vorgeschichte
- HIGH BLOOD PRESSURE, CHOLESTEROL, DIABETES, VITAMIN DEFICIENCY
- Andere Medikamente
- AMLODIPINE, ASPIRIN, ATORVASTATIN, VITAMIN D3, GLIPIZIDE, LORATIDINE, LOSARTAN, METFORMIN, IBUPROFEN, TRAZODONE, LISINOPRIL
- Allergien
- NO KNOWN ALLERGIES
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 06.07.2022
- Impfdatum
- 02.04.2022
- Beginn
- 22.04.2022
- Tage bis Beginn
- 20,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Amnesia
Balance disorder
Cerebrovascular accident
Disorientation
Fatigue
Headache
Laboratory test normal
Malaise
Pain in extremity
Symptomtext
Initially I had some arm pain and felt ill for 10 hours after receiving the vaccine. Then, within a few days, I developed headaches, disorientation and loss of balance. 3 weeks later I had a stroke. I was hospitalized for 2 days. I have been given a different regimen of medication. Numerous tests have been done to rule out underlying conditions that could have caused the stroke and all came back negative. I am still having some lingering effects from the stroke like loss of memory and general fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cerebrovascular accident
- Hospital-Tage
- 2,0
- Labordaten
- Numerous tests to rule out underlying conditions that could have caused the stroke: all negative.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Gout; Slightly High Blood Pressure; Hypothyroidism
- Andere Medikamente
- Levothyroxine; losartan potassium; allopurinol; vitamin C; zinc
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 25.03.2022
- Impfdatum
- 28.01.2022
- Beginn
- 30.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Abdominal pain
Bladder catheter replacement
Catheter removal
Death
Device leakage
Diarrhoea
Hypotension
Symptomtext
ED visit for Urinary catheter leaking - removed and replaced. Hospital admission @ 1 month later - admitted to superior hospital 2/28 through 3/1 for abdominal pain and diarrhea but transfer to hospital after having episodes of hypotension requiring vasoactive medications. He passed away on 3/1. ED visit, hospital admission and death within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NM
- Alter
- 84,0
- Geschlecht
- M
- Eingang
- 02.03.2022
- Impfdatum
- 02.02.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angiogram pulmonary normal
Cardiac arrest
Chest X-ray normal
Death
Resuscitation
Troponin increased
Unresponsive to stimuli
Symptomtext
Death. Pt found unresponsive by son, EMS called, pt had pulse but on way to ED found to be in asystole, CPR/Epi with ROSC. The family chose comfort care on 2/5/2022 and the patient was pronounced dead on 2/5/2022 at 1450
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cardiac arrest
- Hospital-Tage
- -
- Labordaten
- CXR negative acute cardiopulmonary process, CTA negative for PE, troponin elevation.
- Aktuelle Erkrankungen
- None known
- Vorgeschichte
- History of NSTEMI 2020, hypertension, COPD on 4L baseline, chronic pain
- Andere Medikamente
- aspirin, atorvastatin, hydralazine, hydrochlorothiazide, levothyroxine, lisinopril, oxycodone
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 02.01.2022
- Beginn
- 02.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Acute respiratory failure
Dysstasia
Endotracheal intubation
Fall
Grip strength decreased
Asthenia
Chest X-ray
Computerised tomogram abdomen
Computerised tomogram head
Computerised tomogram neck
Computerised tomogram thorax
Dysphagia
Guillain-Barre syndrome
Hypoxia
Immunoglobulin therapy
Intensive care
Mechanical ventilation
Musculoskeletal disorder
Symptomtext
Patient experienced loss of control of arms and legs with tingling in arms and fingers and couldn't hold anything the same day of receiving the vaccine (1/2). She fell twice on 1/7 with difficulty standing back up and also experienced urinary retention. She was admitted to hospital on 1/8 and was started on IVIG on 1/11; respiratory status worsened and she was intubated 1/11. She was transferred to a different hospitals NSICU on 1/12 for further care, including mechanical ventilation and eventual tracheostomy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension, depression
- Andere Medikamente
- Amlodipine 10 mg daily, sertraline 25 mg daily, fish oil 1200 mg daily, vit D
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 23.03.2021
- Beginn
- 02.10.2022
- Tage bis Beginn
- 558,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Amnesia
Blood creatinine increased
Chest X-ray normal
Computerised tomogram head normal
Haemodialysis
Haemoglobin decreased
Hypotension
Laboratory test
SARS-CoV-2 test positive
Syncope
Troponin
Symptomtext
This is a 72y.o. male with PMH significant for ESRD on HD T/T/S, HTN, DM, CVA, BPH, GERD, HLD who was sent to ED from a center for syncopal episode while getting HD. The patient doesn't recall the event, he only remembers that he had breakfast prior to HD and went to his session as usual, he says he was told he had completed HD session. Per primary note he had another syncopal episode 3 weeks ago due to low BP. ED his vitals were stable, labs showed creatinine 4.29, trop 0.04, hgb 10.5. CXR unremarkable. Head CT no acute process. He was admitted to medicine for further management, nephrology is consulted to resume HD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- 10/2 SARS-CoV-2 -COVID-19 by NAA, Micro -- detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 25.09.2022
- Impfdatum
- 17.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Abdominal lymphadenopathy
Abdominal operation
Abdominal pain
Biopsy lymph gland abnormal
Blood alkaline phosphatase increased
Carditis
Chest pain
Colonoscopy
Computerised tomogram
Dyspnoea
Eating disorder
Echocardiogram
Electrocardiogram
Electrocardiogram ambulatory
Erythema
Extrasystoles
Gastritis
Gastrointestinal pain
Symptomtext
Multi-organ inflammatory reaction: -Inflammation of the heart: skip beats, speed up, slow down, chest pain, out of breathe -Enlarged lymph nodes -Inflammation in the mesentery: severe gut pain and constant nausea for over 4months! Could hardly eat. Very sick. Persistent enlarged lymph nodes in the mesentery: not lymphoma. Biopsy showed necrosis! (Death) and granuloma inflammation. -Entire esophagus & stomach lining Red & inflammed -Tiny blood clots coming from GI tract exactly 2 weeks and 1 day after 1st and 2nd doses. -Liver pain and raised ALP -Enlarged spleen & spleen pain -Lung nodules Enlarged lymph nodes persist past 8 months and continue. Nausea improved but persistent. Heart improved after 4 months
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- 2,0
- Labordaten
- CT exam-2/3/22 EKG 2/22 Holt heart monitor 3/22 Heart Echo 3/22 Colonoscopy & scope 3/15/22 Cardiac MRI-4/6/22 CT exam 4/29/22 CT exam 7/8/22 Abdominal surgery- lymph node biopsy 8/9/22 Pathology results of lymph node & surrounding tissue Lots of labs inbetween all that!
- Aktuelle Erkrankungen
- None. Was nursing though.
- Vorgeschichte
- Inflammatory Arthritis
- Andere Medikamente
- None
- Allergien
- Intolerance to egg, dairy, chicken.
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 08.04.2022
- 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: ja
Amnesia
Confusional state
Fatigue
Influenza like illness
Loss of consciousness
Memory impairment
Movement disorder
Speech disorder
Symptomtext
One hour after vaccine administration, patient suddenly lost consciousness while sitting at his computer. After a short period of time, he woke up with his head laying on his keyboard after his wife found him. Upon waking up he reported confusion, an inability to remember where he was/the time/who he was, and an inability to communicate verbally. He was also unable to move his body. Emergency medical services were called, and his initial workup with them was apparently negative. At some point, he was so scared that he did not think he would survive this incident. He also endorsed some flu-like symptoms. He is not able to recall the entire event due to memory loss. The day after the event (the day in which he reported the event to local Pharmacy), he was back to his baseline (i.e. able to speak, move, communicate coherently, etc.) but was still experiencing latent flu-like symptoms and fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Prescriptions: -Alprazolam 0.5 mg, once daily as needed -Solifenacin succinate 5mg, once daily -Gabapentin 300 mg, one capsule three times daily -Sildenafil 100 mg, one tablet daily as need -Venlafaxine ER 75 mg one daily + venlafaxine ER 3
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 15.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Gait inability
Hypoaesthesia
Malaise
Paralysis
Urinary incontinence
Symptomtext
After 48 hours of the vaccine, patient was very ill, she could not walk, both legs are numb, and experienced urinary incontinence. She is partially paralyzed from the vaccine. Right now, she is seeing physical therapy to help her recovery from normal daily activities.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paralysis
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 15.03.2022
- Impfdatum
- 16.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Blood test
Chest X-ray
Computerised tomogram
Contusion
Deep vein thrombosis
Magnetic resonance imaging
Pain
Swelling
Ultrasound scan
Symptomtext
DVT left arm, swelling, bruising and pain Anti-coagulant/blood thinner daily Monthly monitoring of blood clot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deep vein thrombosis
- Hospital-Tage
- 3,0
- Labordaten
- chest x-ray, ulta-sound, MRI, Cat scan, blood work in hospital and admission
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 31.01.2022
- Beginn
- 31.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Dyspnoea
Feeling abnormal
Malaise
Paraesthesia
Paraesthesia oral
Seizure
Tongue disorder
Symptomtext
Moderna covid vaccine was given 1/31/22 at 1:42 PM. Within minutes patient stated she wasn't feeling well. Said she had tingling sensation in her left arm. I then asked about throat, tongue swelling, and breathing. She said her tongue felt thick and was tingling. Instructed technician to call 911. I administered 50 mg oral diphenhydramine solution. Patient said she was still feeling strange. Prepared epipen for administration. Started to monitor blood pressure and pulse, unable to get reading because Patient began to seize. We administered epipen. Patient continued to go in and out of seizures. She was able to communicate between seizures. EMT arrived and transported to a local Emergency room. Spoke to patient 2/1/22. She was kept at ER for approximately 8 hours to be monitored. She knew they gave her famotidine and a steroid. Followed up with patient 2/9/22. She stated she had to go back to ER 2/2/22 at approximately 11pm because she was feeling short of breath and tingly again. Said they gave her famotidine, steroid, and antihistamine again and monitored her. She was released and has had no symptoms since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- do not have hospital records
- Aktuelle Erkrankungen
- COVID 01/04/22
- Vorgeschichte
- HYPOTHYROIDISM, HYPERTENSION, PCOS
- Andere Medikamente
- BUPROPION XL 300, PROPRANOLOL 80, LEVOTHYROXINE 75MCG
- Allergien
- PENICILLIN, PROMETHAZINE, GLUTEN
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 08.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 19,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Chest X-ray normal
Chest pain
Electrocardiogram normal
Fibrin D dimer normal
Painful respiration
Pericarditis
Pleuritic pain
Troponin increased
Ultrasound scan normal
Symptomtext
Seen ER 2/7/22 by Dr, sudden onsent of pleuritic chest pain, positional , sharp stabbing left side check with numbness radiating into left arm, hurts when pushes on chest or takes deep breathe, no previous history of or of pericarditis, long history of abdominal pain for few years, CXR no acute findings, beside ultrasound shows no pericardial effusion, troponin mildly elevated, D-dimer negative, EKG shows no new ischemia, case discussed with cardiology Dr, no regional beds available to admit, discussed with pt, fiance and mother, discharged with close follow up, Toradol IV given with decrease pain, outpt. echo in next day or two, trend toponins as outpatient, ibuprofen for pericarditis,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pericarditis
- Hospital-Tage
- -
- Labordaten
- will discharge home, cardiology appointment in next week.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 08.01.2022
- Beginn
- 30.01.2022
- Tage bis Beginn
- 22,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bell's palsy
Facial paralysis
Facial paresis
Headache
Neurological examination
Pain in jaw
Tinnitus
Symptomtext
Exactly 3 weeks after receiving my booster, I started having left-sided facial weakness. I ended up going to the ER and they diagnosed me with Bell?s palsy. I have not had Covid, nor have I been sick in the last year. I now have a significant left facial droop, ringing in my ears, jaw pain, headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- Emergency room assessment by ER Dr. and neurologist. Diagnosis was confirmed by my PCP
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 41,0
- Geschlecht
- M
- Eingang
- 29.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Fall
Heart rate increased
Hyperhidrosis
Loss of consciousness
Symptomtext
Patient received first dose of Moderna vaccine, complained of light headedness, fast heart rate, chills and sweating and ended up passing out and falling. 911 was called. This lasted about 20 minutes after which the patient felt better and was discharged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Loss of consciousness
Symptomtext
patient passed out about 5 minutes after vaccination. 911 was called, patient was put in a comfortable position by the parent, but woke up immediately after, he was given water and Benadryl but refused. 911 personnel came and attended fully to the patient, then took him to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 15.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Loss of consciousness
Symptomtext
Patient attempted to get up after administration of the vaccine and Passed out
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fall
Head injury
Swelling
Syncope
Symptomtext
AFTER RECEIVING FIRST DOSE OF MODERNA, PATIENT STOOD UP AND WALKED AWAY FROM VACCINE BOOTH. HE BECAME FAINT AND FELL TO THE FLOOR, HITTING HIS HEAD. HE DID NOT LOSE CONSCIOUSNESS BUT EMS WAS CONTACTED. BY THE TIME EMS ARRIVED, APPROXIMATELY 20 MINUTES LATER, PATIENT WAS SITTING IN CHAIR AND HAD A RAISED BUMP ON HEAD FROM FALL. HE STATED HE FELT FINE AND REFUSED EMS TREATMENT.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- NOT KNOWN
- Allergien
- NO ALLERGIES STATED;NKA
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 13.01.2021
- Beginn
- 13.01.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Seizure
Symptomtext
patient had a seizure after receiving the vaccine. no treatment. emt came and assessed patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- epilepsy
- Vorgeschichte
- epilepsy
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Condition aggravated
Seizure
Symptomtext
after administering pts 2nd moderna covid vaccine, pt was instructed to wait for 15 minutes in the waiting area. While the pt was waiting he signaled me over and indicated that he felt as if he was about to have a seizure. As I was calling EMS a technician stayed with the pt. He had 2 seizing episodes while seated in the waiting area until EMS arrived. Pt then left with EMS on stretcher
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- history of seizures
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Condition aggravated
Dizziness
Electrocardiogram
Interchange of vaccine products
Loss of consciousness
Musculoskeletal stiffness
Syncope
Tremor
Unresponsive to stimuli
Symptomtext
Patient had a vasovagal syncope rxn. He had it marked on his questionnaire. I asked him and he said it only happened once and was due to being nervous getting the J 7 J 1st dose. I talked to him for a minute to see how he was feeling and he said anxious but thought he would be fine this time. I tried to get him to focus on something other than the shot. I told him to count to 10. As soon as he started counting as a distraction, I gave him the shot. He seemed fine, but I asked to make sure. He said he was fine, we talked for a moment and I asked him was doing ok, which he said he was. I asked if he was ready or wanted to wait a minute. He said he thought he was fine. I told him no rush. He then said he was feeling a little light headed, so I got him a water. Then he passed out and stiffened up and had tremors. I tried talking to him and he was unresponsive. I had Employee call Emergency. It took about 2 minutes before he seemed to gain his wits. A manager came in and was talking to him. I told them we called Emergency. We asked if he wanted medical attention. Initially he said no, but when they showed up he decided to let them check him out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- The EMT's checked his BP, HR and ran an EKG. They recommended he go to the hospital for a follow up. He declined. The EMT did say he believed it was a vasovagal syncope event. After about 15 minutes, he seemed fully aware and appeared much better. The EMT's again recommended he get checked out, but he said he was fine and signed saying he felt fine.
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- None
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE ACCORDING TO VACCINE QUESTIONNAIRE
- Vorherige Impfungen
- only the J & J shot that he received on 5/11/2021, He was 20. Similar rxn according to patient
- Staat
- SC
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Fall
Head injury
Seizure
Syncope
Symptomtext
Patient had dizziness, lightheadedness, and fainted about 15 minutes after receiving vaccine. She hit her head and had seizure about 1 minute after fall
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Seizure
- Hospital-Tage
- -
- Labordaten
- EMT responded and assessed patient before releasing her to her husband
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- Patient fainted after receiving 2nd dose of Moderna at age 35
- Staat
- -
- Alter
- 97,0
- Geschlecht
- F
- Eingang
- 23.05.2023
- Impfdatum
- 02.02.2022
- Beginn
- 25.09.2022
- Tage bis Beginn
- 235,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypotension
Symptomtext
I95.89 CHRONIC HYPOTENSION 10/12/2022 HX OF TRANSIENT ISCHEMIA ATTACK I95.9 HYPOTENSION 9/25/2022 HX OF TRANSIENT ISCHEMIA ATTACK
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 21.12.2022
- Impfdatum
- 21.01.2022
- Beginn
- 09.12.2022
- Tage bis Beginn
- 322,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
Genitourinary symptom
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 11/25/2022 - 12/9/2022 (14 days) Presentation to the ED: shortness of breath & UTI symptoms. COVID + date: 12/9/2022 Treatment: none, patient was asymptomatic. tested positive on a transfer screen required to return to SNF. Discharge to: SNF Moderna Lot # 046B21A 4/23/2021 Moderna Lot # 003C21A 5/21/2021 Moderna Lot # 001J212A 1/21/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DM
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 01.10.2022
- Impfdatum
- 02.01.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 89,0
- Dosis
- 4
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Hypertension
Memory impairment
Symptomtext
Patient has become forgetful after Covid-19 infection.; high blood pressure which started in April of 2022 and may be related to her Covid-19 infection.; patient caught Covid-19 after her first Moderna Covid-19 booster dose.; This spontaneous case was reported by a patient and describes the occurrence of MEMORY IMPAIRMENT (Patient has become forgetful after Covid-19 infection.), HYPERTENSION (high blood pressure which started in April of 2022 and may be related to her Covid-19 infection.) and COVID-19 (patient caught Covid-19 after her first Moderna Covid-19 booster dose.) in a 77-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 001J212A and 053B22A) for COVID-19 vaccination. No medical history was provided by the reporter. Concurrent medical conditions included Hypertension and Hypercholesteremia. Concomitant products included METOPROLOL and PARACETAMOL (TYLENOL) for an unknown indication. On 02-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Aug-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In April 2022, the patient experienced HYPERTENSION (high blood pressure which started in April of 2022 and may be related to her Covid-19 infection.) and COVID-19 (patient caught Covid-19 after her first Moderna Covid-19 booster dose.). On an unknown date, the patient experienced MEMORY IMPAIRMENT (Patient has become forgetful after Covid-19 infection.). At the time of the report, MEMORY IMPAIRMENT (Patient has become forgetful after Covid-19 infection.), HYPERTENSION (high blood pressure which started in April of 2022 and may be related to her Covid-19 infection.) and COVID-19 (patient caught Covid-19 after her first Moderna Covid-19 booster dose.) outcome was unknown. Patient was using unspecified high Cholesterol medication as a concomitant product. Patient was experienced Fever, cough, muscular weakness and headache as a symptom of covid-19. All the events were experienced after the covid-19 infection. No treatment information was provided by the reporter. The patient had headaches and high blood pressure which started in April of 2022 and may be related to her Covid-19 infection. This case was linked to US-MODERNATX, INC.-MOD-2022-653180, US-MODERNATX, INC.-MOD-2022-653189 (E2B Linked Report).; Sender's Comments: US-MODERNATX, INC.-MOD-2022-653180:Dose 1 US-MODERNATX, INC.-MOD-2022-653189:Dose 2
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Hypercholesteremia; Hypertension
- Vorgeschichte
- Comments: No medical history was provided by the reporter.
- Andere Medikamente
- METOPROLOL; TYLENOL
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 07.09.2022
- Impfdatum
- 13.03.2021
- Beginn
- 05.08.2022
- Tage bis Beginn
- 510,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Atrial fibrillation
COVID-19
Dizziness
Electrocardiogram ST-T segment abnormal
Electrocardiogram abnormal
Femur fracture
Musculoskeletal disorder
Palpitations
Periprosthetic fracture
SARS-CoV-2 test positive
Sinus rhythm
Tachycardia
Symptomtext
80 y/o female with a history of CAD by CTA 2015, hx of multiple PE's in 2015 on coumadin, PHT, HTN, HLD, GERD, CKD, and COPD who presented to the EC on 8/5 for knee pain after her legs gave out while bending down to pick up an object. Found to have a periprosthetic nondisplaced medial femoral condyle Fracture. Also found to be positive for COVID on admission. During admission developed atrial fibrillation with RVR. On 8/13 she was RRT for tachycardia with palpitations and lightheadedness. ECG with recurrence of atrial fibrillation with diffuse ST-T abnormalities. She was started on IV amiodarone and her magnesium was supplemented with conversion back to NSR. She is stable for DC to SAR with outpatient follow-up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- 12,0
- Labordaten
- 8/5 SARS-CoV-2 (COVID-19) by Nucleic Acid Amplification, POC --detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 26.07.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.06.2022
- Tage bis Beginn
- 151,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood cholesterol increased
Blood test
Hypertension
Low density lipoprotein increased
Stress
Symptomtext
I don't want to blame my health events on the vaccine but on June 21st of 2022 a stressful event occurred in my life and I knew it was effecting me but I didn't realize how bad it was until 06/24 when I was told by an ENT that my blood pressure was very high. I went to see my doctor and it was still high. She advised that I monitor my blood pressure and if it got to anything higher than 140 over 90 consistently for 2 days to begin taking a medication that she prescribed. I monitored for two days and my readings continued to be high so I've been taking 10mg of amlodipine daily since 07/17/2022. The readings of my blood pressure have improved but are still high. I've only had 1 reading in the advised range since beginning the medication.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- Blood panel, high cholesterol, high LDL levels, 06/29/2022.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Vitamin D3; ZYRTEC; montelukast; levothyroxine; ADDERALL XR; probiotic gummies; azelastine HCI; FLONASE
- Allergien
- WELLBUTRIN; EFFEXOR; AVELOX; gabapentin
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 22.07.2022
- Impfdatum
- 20.01.2022
- Beginn
- 16.06.2022
- Tage bis Beginn
- 147,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chills
Dizziness
Ear infection
Ear pain
Fatigue
Feeling cold
Headache
Lethargy
Oropharyngeal pain
Productive cough
Pyrexia
Rhinorrhoea
SARS-CoV-2 test positive
Sneezing
Tremor
Symptomtext
Starting 06/16/2022, I woke up at 06:00AM with a sore throat. I did the at home test and it was negative. So, I got on the plane with a mask. I arrived at 03:00PM and felt even worse. Later, I had a headache, "on fire" sore throat, left earache and bad fatigue. I was so fatigued that evening. I know I broke a fever that evening because I could not get warm. I had chills and was shaking. The next morning I woke up and felt dizzy. I didn't know where I was and had to grasp the wall. I went to the bathroom and tested my temp (102.5) and (101.2). I went back to bed and at 08:00AM I called my doctor and they got me a telehealth visit. So, about 30 min before the visit I did my 2nd at home test which came back positive. So, I saw the doctor and she recommended I take PAXLOVID, isolate for 5 days and take ibuprofen. She also called me in an antibiotic for an ear infection and cough medicine. I could feel myself getting worse and becoming more fatigued and I was shaky, lethargic, had a headache and fever. I got the PAXLOVID and took it right away. 30 minutes after taking it I started feeling better and that feeling would come and go in waves. She gave me something for pain but I did not need it. I did develop a cough but it was never a phlegmy cough. I did need the cough medicine but not much. Saturday 06/18/2022, I started the antibiotic (possibly ciprofloxacin) for the ear infection because the ear pain would not stop. I was still taking the PAXLOVID at this time and I was coming out of it on 06/19/2022. I was more coherent and was feeling better by 06/20/2022. I finished the PAXLOVID as instructed and on 06/21/2022 I was feeling better. The only thing that I experienced after stopping the PAXLOVID was a runny nose and some sneezing which lasted for about 2 days then resolved. I have felt fine ever since.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- At-home COVID-19 test (06/16/2022): positive; at-home COVID-19 test (06/17/2022): positive.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- High Blood Pressure
- Andere Medikamente
- Multivitamin; zinc; magnesium; AZOR; omega 3; ibuprofen
- Allergien
- Sulfa; diphenhydramine; aspirin
- Vorherige Impfungen
- -
- Staat
- MT
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 13.07.2022
- Impfdatum
- 12.04.2022
- Beginn
- 09.06.2022
- Tage bis Beginn
- 58,0
- Dosis
- 4
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Chest X-ray normal
Chest discomfort
Dyspnoea
Electrocardiogram normal
Fibrin D dimer normal
Laboratory test normal
Symptomtext
My symptoms were when I laid down I my chest felt tight like a vice grip had a hold and I couldn't catch my breath. This has happened June 9th, June 24th, June 25 and July 12th. I may have happened prior to June 9th but not bad enough to go the the ER. On each date I went to the ER but all tests that they ran were normal. The doctor increased your Nexium and Metropole in case it was my acid reflux that causing the issue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- 3,0
- Labordaten
- EKG, normal; Chest XRay, normal; Blood Panel, normal; DDimer, normal
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Skin graphs from burns; stint in heart;
- Andere Medikamente
- Acetaminophen; Acyclovir; Amoxicillin; Apixaban; Aspirin; Atorvastatin; Benzonatate; Cetirizine; CPap; Duloxetine; Esomeprazole; Gabapentin; Losartan; Metoprolol; Multi Vitamin; Naproxen; NDansetrion; Pramipexol; GasX; Sumatriptan; Cialis;
- Allergien
- Delotid; Ketamine; Sage
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 17.06.2022
- Impfdatum
- 11.05.2021
- Beginn
- 12.05.2022
- Tage bis Beginn
- 366,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chronic obstructive pulmonary disease
Condition aggravated
Hypoxia
SARS-CoV-2 test positive
Symptomtext
Hospitalization on dates 5/12/2022- 5/21/2022 for hypoxemia likely secondary to COPD exacerbation, positive for COVID 5/13/2022 . Treated with dexamethasone, methylprednisolone, prednisone
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- tramadol, stress test dye
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Body temperature
Chest pain
Cough
Nasal congestion
Pyrexia
Symptomtext
small cough; chest hurt; felt a little stuffy for about a week; 103-104 fever for 3 or 4 days; This spontaneous case was reported by a consumer and describes the occurrence of COUGH (small cough), CHEST PAIN (chest hurt), NASAL CONGESTION (felt a little stuffy for about a week) and PYREXIA (103-104 fever for 3 or 4 days) in a 54-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 18-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 18-Jan-2022, the patient experienced COUGH (small cough), CHEST PAIN (chest hurt), NASAL CONGESTION (felt a little stuffy for about a week) and PYREXIA (103-104 fever for 3 or 4 days). At the time of the report, COUGH (small cough) and CHEST PAIN (chest hurt) outcome was unknown and NASAL CONGESTION (felt a little stuffy for about a week) and PYREXIA (103-104 fever for 3 or 4 days) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature: 103-104 (High) 103-104 fever. No Concomitant product use was reported. The patient after getting the Moderna booster dose on 18-Jan-2022, began to experience side effects as well. The patient had a 103-104 fever for 3 or 4 days and also stated that the patient had a small cough, their chest hurt, and the patient felt a little stuffy for about a week. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Test Name: Body temperature; Result Unstructured Data: 103-104 fever
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 18.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Metastases to lung
Oxygen saturation
Symptomtext
Woke up the following night and couldn't breathe/Had hard time breathing, like couldn't catch breathe/It felt like could not get enough oxygen and was gasping for air; This spontaneous case was reported by a patient and describes the occurrence of DYSPNOEA (Woke up the following night and couldn't breathe/Had hard time breathing, like couldn't catch breathe/It felt like could not get enough oxygen and was gasping for air) in a 63-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J21-2A) for COVID-19 vaccination. The patient's past medical history included Nephrectomy (One of kidneys removed). Concurrent medical conditions included Blood pressure, Immunocompromised, Renal cell carcinoma and Metastases to lung (Cancer was metastasized to lungs and started a treatment of Keytruda 2 days after the booster (20-Jan-2022)). On 18-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 19-Jan-2022, the patient experienced DYSPNOEA (Woke up the following night and couldn't breathe/Had hard time breathing, like couldn't catch breathe/It felt like could not get enough oxygen and was gasping for air). The patient was treated with PEMBROLIZUMAB (KEYTRUDA) on 20-Jan-2022 for Metastases to lung, at an unspecified dose and frequency. At the time of the report, DYSPNOEA (Woke up the following night and couldn't breathe/Had hard time breathing, like couldn't catch breathe/It felt like could not get enough oxygen and was gasping for air) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Oxygen saturation: 93/94% O2 levels were 93/94%. Patient took concomitant medications for blood pressure. Patient report that after getting the Moderna booster dose, he began to experience some side effects. He woke up the following night and could not breathe. He had hard time breathing, like he could not catch my breathe. It felt like could not get enough oxygen and was gasping for air. He indicated that he was still having same problem but not as bad at the time of report. He also stated that he had been to the ER, they could not anything wrong. He stated that his cancer was metastasized to his lungs and started a treatment of Keytruda. Keytruda can also cause respiratory issues, but patient was experiencing these before he got that treatment. Treatment for the event included inhaler. This case was linked to MOD-2022-541254.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Name: O2 level; Result Unstructured Data: O2 levels were 93/94%
- Aktuelle Erkrankungen
- Blood pressure; Immunocompromised; Metastases to lung (Cancer was metastasized to lungs and started a treatment of Keytruda 2 days after the booster (20-Jan-2022)); Renal cell carcinoma
- Vorgeschichte
- Medical History/Concurrent Conditions: Nephrectomy (One of kidneys removed)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 21.04.2022
- Impfdatum
- 18.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dyspnoea
Metastases to lung
Oxygen saturation
Symptomtext
Woke up the following night and couldn't breathe/Had hard time breathing, like couldn't catch breathe/It felt like could not get enough oxygen and was gasping for air; This spontaneous case was reported by a patient and describes the occurrence of DYSPNOEA (Woke up the following night and couldn't breathe/Had hard time breathing, like couldn't catch breathe/It felt like could not get enough oxygen and was gasping for air) in a 63-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J21-2A) for COVID-19 vaccination. The patient's past medical history included Nephrectomy (One of kidneys removed). Concurrent medical conditions included Blood pressure, Immunocompromised, Renal cell carcinoma and Metastases to lung (Cancer was metastasized to lungs and started a treatment of Keytruda 2 days after the booster (20-Jan-2022)). On 18-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On 19-Jan-2022, the patient experienced DYSPNOEA (Woke up the following night and couldn't breathe/Had hard time breathing, like couldn't catch breathe/It felt like could not get enough oxygen and was gasping for air). The patient was treated with PEMBROLIZUMAB (KEYTRUDA) on 20-Jan-2022 for Metastases to lung, at an unspecified dose and frequency. At the time of the report, DYSPNOEA (Woke up the following night and couldn't breathe/Had hard time breathing, like couldn't catch breathe/It felt like could not get enough oxygen and was gasping for air) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Oxygen saturation: 93/94% O2 levels were 93/94%. Patient took concomitant medications for blood pressure. Patient report that after getting the Moderna booster dose, he began to experience some side effects. He woke up the following night and could not breathe. He had hard time breathing, like he could not catch my breathe. It felt like could not get enough oxygen and was gasping for air. He indicated that he was still having same problem but not as bad at the time of report. He also stated that he had been to the ER, they could not anything wrong. He stated that his cancer was metastasized to his lungs and started a treatment of Keytruda. Keytruda can also cause respiratory issues, but patient was experiencing these before he got that treatment. Treatment for the event included inhaler. This case was linked to MOD-2022-541254.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Test Name: O2 level; Result Unstructured Data: O2 levels were 93/94%
- Aktuelle Erkrankungen
- Blood pressure; Immunocompromised; Metastases to lung (Cancer was metastasized to lungs and started a treatment of Keytruda 2 days after the booster (20-Jan-2022)); Renal cell carcinoma
- Vorgeschichte
- Medical History/Concurrent Conditions: Nephrectomy (One of kidneys removed)
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 28.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test
Condition aggravated
Diabetes mellitus
Fatigue
Somnolence
Symptomtext
I was very tired & very sleepy all the time it felt like I was drained. I was already pre-diabetic but now I am diabetic & on meds.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Bloodwork-All
- Aktuelle Erkrankungen
- one
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- Amlodipine, Atorvastatin, Metoprolol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 07.04.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Paraesthesia
Symptomtext
I have had periodic numbness and tingling in my hands and feet since receiving the Covid vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- spironolactone, tretinoin, dapsone, multivitamin
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 18.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Cardiac failure chronic
Cardiac failure congestive
Chronic obstructive pulmonary disease
Dyspnoea exertional
Symptomtext
Patient presented to the ED for dyspnea on exertion and COPD on 1/28/22. Patient presented to the ED and was subsequently hospitalized for chronic congestive heart failure. These visits are within 6 weeks of receiving covid vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea exertional
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 15.03.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Alanine aminotransferase increased
Amino acid level
Blood bilirubin increased
Blood calcium normal
Blood electrolytes normal
Blood magnesium normal
Blood testosterone normal
Blood thyroid stimulating hormone normal
Burning sensation
Chest pain
Dysgeusia
Exposure to extreme temperature
Feeling cold
Feeling hot
Full blood count normal
Magnetic resonance imaging spinal normal
Paraesthesia
Paraesthesia oral
Symptomtext
Around January 17th 2022 - Initially it felt like cold air was intermittently rushing over my right quad muscle with pants on. That lasted for about 1 week and then it developed in the other quad muscle. Again when I had long pants on. February 19th I was exposed to extreme cold in my fingers and face. The rest of the body was covered up. February 21 I was woken up from sleep with the feeling that my outer left leg was cold and air was rushing over it. I was under the covers. This progressed to the other leg , both hands/fingertips tingled, my face/lips and tongue started to tingle and still do. Bottom of my feet burn and feel hot. Slight metallic taste in my mouth occurs periodically. The burning sensation progressed to groin and chest 3/15/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Normal labs : electrolytes, kidney function, Vit B12, methylmalonic acid, T4/TSH, testoterone, Vit D, CBC, Calcium , magnesium Abnormal labs: ALT elevated 2 points over normal and TBili 1.2 (normal 1.0) RAdiology: X-ray -mild to moderate degenerative arthritis at C-5 thru C-7. MRI of C-spine: normal. No nerve impingement
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- ulcerative colitis, BPH, chronic allergies
- Andere Medikamente
- mesalamine 800 mg BID, citalopram 20mg QD, Loratadine 10mg QD, montelukast 10mg QD, Fish oil 2gm daily, multivitamin 1 QD, tamsulosin 0.4mg BID, glucosamine/chondroitin 2 tabs daily.
- Allergien
- environmental. tree pollen, dist mites, mold, cats
- Vorherige Impfungen
- Severe dizziness that did not respond to labyrinthine maneuvers diagnoses as Disembarkment syndrome in April 2021 after vaccine
- Staat
- GA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 13.03.2022
- Impfdatum
- 10.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dehydration
Dizziness
Pyrexia
Symptomtext
Pt experienced high fever for 4 days post vaccine. 102 degrees, dizziness, dehydration
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dehydration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Dupixent
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 01.03.2022
- Impfdatum
- 16.02.2022
- Beginn
- 27.02.2022
- Tage bis Beginn
- 11,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Abortion spontaneous
Blood test
Dizziness
Exposure during pregnancy
Feeling cold
Haemorrhage
Headache
Pyrexia
Tremor
Ultrasound scan
Symptomtext
She got her vaccine, she was having very bad shakes, was kind of cold and running a fever, and having a headache. She didn't feel super dizzy. A week after her vaccine she was bleeding (pregnant) and was diagnosed as having a miscarriage. She was 9 1/2 weeks pregnant. The hospital did an ultrasound and some blood work and they did not find a heart beat on the US. She is currently bleeding but it's like a period, doesn't know if she is passing it or not, but has an APT today to see the doctor to see what is going to happen from there.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- US and blood work.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Anxiety.
- Andere Medikamente
- Prenatal vitamins, Celexa.
- Allergien
- None.
- Vorherige Impfungen
- Got the flu after receiving the flu shot when she got her first COVID shot 1/19/22.
- Staat
- PA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 26.02.2022
- Impfdatum
- 16.01.2022
- Beginn
- 23.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect route of product administration
Joint range of motion decreased
Mobility decreased
Pain in extremity
Symptomtext
1 week after receiving Moderna booster, patient experienced difficulty moving her right arm. She does not have full range of motion. She cannot put her arm behind her back and has some pain in her right arm. Last week she asked about it and all the doctor said was maybe the pharmacist hit a bone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- Cough from COPD
- Vorgeschichte
- COPD, high blood pressure
- Andere Medikamente
- Losartan/HCTZ, Brovana, Budesonide inhalant solution, multivitamins
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 25.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 13.02.2022
- Tage bis Beginn
- 5,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Sleep disorder
Urticaria
Symptomtext
Originally received a shot in July-August of 2021, and shortly moved in to a new residence. Started getting breakouts of hives, mostly on my left shoulder, my upper back, and the insides both arms/forearms/armpits. They would always flare up especially bad late at night, shortly before going to bed Originally believed it was some other element, such as a food or fragrant chemicals that I may be having a reaction to, or that it may be stress-induced hives. Took a regimen of medication (cannot recall at the moment the exact intake, but it was about twenty pills over six days) that helped boost my immune system, and then wean me off to a point that it could "calm down" again, and hopefully the hives would go with it, as was described by my nurse. After the regimen, my hives calmed down but never went away completely, though they never flared up like they had been. On February 8th, I received the booster for Moderna (the vaccine listed on this report), and by the end of the week (the earliest I can remember it happening was on the Sunday following), my hives started flaring up again, same pattern as before, but much worse than last time. Now, they're all down my back, down the sides and inside of my legs and knees, on the top of my feet, the backs of my hands, on my upper chest and belly, on my forehead and back of head underneath my hair, as well as all the same places they were showing up before. They also itch much worse, to the point that it is sometimes difficult to fall asleep because of them. Due to the similar time both flare ups occurred after getting a vaccine, my nurse came to the conclusion it was happening due to the vaccine or an ingredient in the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Just the Moderna vaccine and booster shots.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Vitamin C supplements (Nature Made brand)
- Allergien
- -
- Vorherige Impfungen
- Moderna. Hives.
- Staat
- -
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 20.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 8,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Electrocardiogram
Electrocardiogram QT prolonged
Electrocardiogram T wave abnormal
Electrocardiogram normal
Fall
Hypotension
Memory impairment
Neck pain
QRS axis normal
Unresponsive to stimuli
Symptomtext
EMS reports patient was walking this evening 01/28/2022 when his feet slipped out from under him and he fell. His family notes that they were with him but they are not sure if he hit his head or lost consciousness. He remained outside for an unknown amount of time before his family could get him inside. He does not remember much of the fall and is not able to provide details of he events before or after the fall. He notes that he had 3 drinks prior to arrival. He is complaining of some neck pain but does not admit to any other pain. EMS noted that the patient was hypotensive to the 80s systolic en route and had a brief 1 minute episode in which he went unresponsive, staring off to the left side. Patient received a second covid vaccine on 01/20/2022. Per guidelines, all hospitalization are reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- 1,0
- Labordaten
- EKG 12-LEAD Date/Time: 1/28/2022 9:06 PM ECG reviewed by ED Physician in the absence of a cardiologist: yes Rate: ECG rate: 75 ECG rate assessment: normal Rhythm: Rhythm: sinus rhythm QRS: QRS axis: Normal Comments: Prolonged QT. Nonspecific T wave changes.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Cough
Dyspnoea
Fatigue
Nasal congestion
Pain
Pyrexia
Sinus congestion
Symptomtext
Fever of 100.5 and higher. Body aches, sinus passages filled, difficulty breathing. Fever lasted for over 4 days. Stuffy nose, fatigue, and difficulty breathing along with cough continues. Going on 8 days. Making an appointment with family doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- N/A - making appointment with family doctor.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Losartan 50 mg
- Allergien
- mild allergies to chocolate
- Vorherige Impfungen
- Fever & body aches for 24 hours. 62 yrs, 07/06/2021. Covid-19 Moderna. Second shot.
- Staat
- MN
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Anion gap
Blood calcium normal
Blood chloride increased
Blood creatinine normal
Blood glucose normal
Blood potassium normal
Blood sodium normal
Blood urea nitrogen/creatinine ratio
Blood urea normal
Brain natriuretic peptide normal
Carbon dioxide decreased
Chest X-ray normal
Chest discomfort
Dyspnoea
Electrocardiogram abnormal
Full blood count
Haematocrit
Haemoglobin decreased
Symptomtext
Chest tightness, shortness of breath, nausea and vomiting 8:45pm increasingly worse until about 11:30pm with acetaminophen and Zofran.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- Basic Metabolic Panel: NA 137 K 3.7 CL 107 CO2 21 AG 9 GLU 124 CA 9.1 BUN 11 CRE AT 0.81 B/C RATI O 14, Brain Natriuretic Peptide: BRAIN NAT PEPTIDE 12, CBC W PLT NO DIFF: WBC 10.0 RBC 3.97 HGB 11.2 HCT 33.7 MCV 85 MCH 28.2 MCH C 33.2 RDW 13.0 PLT 250 MPV 10.3, Nucleated red blood cells as percent of blood leukocytes: NRBC 0.0 ABS NRBC 0.0, troponin I: TROPI <0.010, EKG 12 lead: normal sinus rhythm right atrial enlargement t wave abnormality consider inferior ischemia abnormal ECG compared to EKG of 19-FEB-2021 rate increased by 27 bpm t wave inversions inferiorly new especially aVF ventricular rate 97bpm atrial rate 97 bpm p-r interval 146ms QRS duration 82ms QT 344ms QTc436ms p axis 78 degrees r axis 81 degrees t axis -22 degrees, x-ray chest 1 view portable: no acute intrathoracic process lungs are clear no appreciable pleural effusion or pneumothorax the cardio mediastinal silhouette is normal the visualized osseous structures are unremarkable. All tests between 11pm 01/26/22 and 1am 01/27/22
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Long Haul Covid (fatigue, brain fog, muscle and joint pain month after contracting Covid-19).
- Andere Medikamente
- CYRED EQ (hormonal birth control pill), vitamins D3, C, B12), magnesium, fish oil
- Allergien
- amoxicillin
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Chest pain
Cyanosis
Dyspnoea
Malaise
Dizziness
Illness
Tremor
Vomiting
Nausea
Pain
Pallor
SARS-CoV-2 test positive
Symptomtext
Approx 8-10 min after vaccine administration, I vomited and remained nauseated for 24 hours. Pallor was present. Approx 4 hours in I had shortness of breath and some cyanosis around my mouth (blue lips as well). I had been sweeping. I stopped and went to lie down. I had a can of ?Oxygen in a can?. I took in some of that over the course of 30 minuets. I started to develop chest pain that I initially attributed to anxiety. But, had felt general malaise the entire time. The chest pain got severe enough I called the ER. I preformed my own ECG and submitted it to the ER. It looked good. My saturation was WNL as well as the rest of my vitals. I started with fairly severe body aches by 11 pm. Those steadily increased and by 2:30-3 PM on the 20th I was in clinic receiving IV fluids and IM pain medication. I struggled with SOB and went in for a COVID swab on Monday 1/24/22. This came out positive. I had been tested the day of my vaccination and had been testing every other day for over a week. 1/25/22 the sob got severe enough I started a prednisone pack I had left over and text my provider about starting that. By the next afternoon, the sob and tightness in my chest began to improve. I am still experiencing fatigue and spinal pain (which I got with my first bout of COVID and each vaccination).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- X-rays will be obtained on my back when I'm well.
- Aktuelle Erkrankungen
- Streptococcus (throat)
- Vorgeschichte
- Have had fatigue resulting from the removal of a parathyroid tumor on 8/2020. Have had chronic spinal pain since the last COVID vaccine
- Andere Medikamente
- Adderall, Lamotrigine,pantoprazol
- Allergien
- None
- Vorherige Impfungen
- Same as above minus the sob and hypoxia. Bith Moderna vaccinations jan 2021 and feb 2021. Aged 43
- Staat
- KY
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 24.01.2022
- Beginn
- 24.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Blood test normal
Bronchospasm
Dysphemia
Electrocardiogram normal
Impaired work ability
Tremor
Symptomtext
Patient was receiving the booster dose while at work. About 1 hour after vaccine was given, patient started to shake and studder during normal conversation with coworkers. Patient left work and went to the urgent care. Where they did not perform any tests and sent her home to rest. They told her that this ADR had been reported 51 times and that it would go away in a few days. The next morning (Tuesday 1/25) patient woke up and starting shaking again around 8am, then she started to studder again starting at 11am uncontrollably. The symptoms would only subside during sleep. The next day (Wed 1/26) patient woke up and symptoms persisted and she decided to visit her physician. During her physician visit they performed an EKG and blood work to try and determine what was going on. All test came back normal. The physician determined that she was having bronchial spasms and sent her home with some Hydroxyzine and it should go away in a few days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- no
- Vorgeschichte
- HTN, Asthma, PCOS
- Andere Medikamente
- Fluticasone, Albuterol, Montelukast, Fluoxetine,Vitamin D3, Amlodipine, Metformin, levocetirizine, Medroxyprogesterone, Omeprazole
- Allergien
- Celexa, HCTZ: Spike in BP for both
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 26.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Fatigue
Hypertension
Symptomtext
High blood pressure spikes throughout day after vaccinated persisting a week after vaccination. Fatigue also present for a week after vaccination
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- High blood pressure . Normal blood pressure for patient is 120/80. Multiple readings showed 178/78, 144/78, 166/79.
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- Vyvanse, adderall
- Allergien
- Peppers
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 23.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Dyspnoea
Heart rate increased
Myalgia
Symptomtext
Shortness of breath, chest pain and muscle soreness over left chest fast heart beat on and off still lasting 3 days later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Biotin, B12
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anxiety
Back pain
Breath sounds abnormal
Chest tube insertion
Dyspnoea
Pneumothorax
Symptomtext
RESIDENT W/O EXERTION/BREATHING DIFFICULTIES, POX 71%-72% WITH O2 AT 2L PER NC. LUNGS SOUNDS DIMINISHED BILATERAL. INCREASED 02 TO 4L PER NC PER PRN TITRATION ORDERS. DUONEB BREATHING TX ADMINISTERED. ANXIOUS AFFECT BUT HE DENIES ANXIETY. POX IMPROVED SOME AFTER BREATHING TX 88%-91% WITH O2 AT 4L PER NC AND STATES HE IS STARTING TO FEEL BETTER. LUNG SOUNDS CONTINUE DIMINISHED BILATERAL. RESIDENT C/O BACK PAIN BEHIND HIS LUNGS. VS 98.4 102 22 128/82. DR. NOTIFIED OF RESIDENTS CONDITION AND WAS INSTRUCTED TO SEND HIM TO ER FOR FURTHER EVAL. CALLED ER TO CHECK ON STATUS OF RESIDENT AND WAS TOLD HE HAD A PNEUMOTHORAX(LEFT) AND WAS HAVING A CHEST TUBE PLACED AT THIS TIME AND WILL BE ADMITTED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- COPD, Dependence on supplemental oxygen, hypothyroidism, hypertension, insomnia, Hyperlipidemia
- Vorgeschichte
- COPD, Hyperlipidemia, DEPENDENCE ON SUPPLEMENTAL OXYGEN, HYPOTHYROIDISM, UNSPECIFIED, ESSENTIAL (PRIMARY) HYPERTENSION, ACQUIRED ABSENCE OF OTHER SPECIFIED PARTS OF DIGESTIVE TRACT, INSOMNIA, UNSPECIFIED
- Andere Medikamente
- Advair Diskus Aerosol Powder Breath Activated 250-50 MCG/DOSE (Fluticasone-Salmeterol) 1 inhalation inhale orally two times a day related to CHRONIC OBSTRUCTIVE PULMONARY DISEASE, UNSPECIFIED Clopidogrel Bisulfate Tablet 75 MG Give 75 mg
- Allergien
- NKDA, NKA
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Chest pain
Epistaxis
Pyrexia
Tongue disorder
Wheezing
Symptomtext
Nose bleeding, chest pain, wheezing, scaled tongue, high fever 41*. These were the same symptoms when received the second dose of Moderna. Not reported previously. Severe joint pain since the first dose a year ago
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 5,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Condition aggravated
Pruritus
Symptomtext
itching of both palms and both of feet; Itching of both palms of hands that gradually got worse; This spontaneous case was reported by a consumer and describes the occurrence of PRURITUS (itching of both palms and both of feet) and CONDITION AGGRAVATED (Itching of both palms of hands that gradually got worse) in a 29-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J212A) for COVID-19 vaccination. No Medical History information was reported. On 10-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 15-Jan-2022, the patient experienced PRURITUS (itching of both palms and both of feet) and CONDITION AGGRAVATED (Itching of both palms of hands that gradually got worse). The patient was treated with HYDROCORTISONE for Adverse event, at an unspecified dose and frequency. At the time of the report, PRURITUS (itching of both palms and both of feet) had not resolved and CONDITION AGGRAVATED (Itching of both palms of hands that gradually got worse) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. No concomitant medications were mentioned. It was stated that patient went to doctor who did not prescribe anything as per patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: ja
Chest discomfort
Condition aggravated
Dyspnoea
Symptomtext
About 13 minutes after the vaccine was given, patient started complaining of chest tightness and trouble breathing. Pt has had multiple severe anaphylatic events due to medications, injections and foods. Patient was immediately escorted over to our ED department for further treatment which is connected to the hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Dry cough, some chest tightness x 2 weeks
- Vorgeschichte
- Asthma
- Andere Medikamente
- Lisinopril, flomax,tramadol
- Allergien
- Bee Venom, Toradol, morphine, PCN, shell fish, strawberry extract, minocycline
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ear pain
Fatigue
Feeling abnormal
Headache
Injected limb mobility decreased
Oedema peripheral
Pain
Pain in extremity
Pyrexia
Symptomtext
I received the vaccine at 8:30 am on 1/14/22. By 8:00 pm that evening, I felt really bad - severe pain in my arm, fever, body aches. On 1/15/22, I could barely lift my left arm as it hurt so bad. I noticed that the left armpit was starting to swell and I ran a 102.3 F. fever all day and had body aches, headache, and fatigue. 1/16/22, fever was down to 100 degrees and body aches started to improve. Armpit was still swollen at this time. On 1/17/22 still felt fatigued and noticed that the swelling in the armpit appeared to be worse than the previous day. 1/18/22 - swelling in armpit is significantly worse and left ear has been hurting as well. Called primary care physician to get checked. Have appointment on 1/19/2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Iodine
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Chest pain
Induration
Injection site pain
Pain in extremity
Peripheral swelling
Skin warm
Tenderness
Symptomtext
injection site pain, full arm pain with swelling and more intense pain in the arm pit and upper chest on left side. Forearm is hard and warm to the touch and also has pain with pain to touch.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- migraines, diverticulosis, hyperlipidemia
- Vorgeschichte
- -
- Andere Medikamente
- lipitor, align probiotic, multivitamin, lo lo estrin FE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Palpitations
Symptomtext
Patient reported a racing heart, pounding heart, and chest ache. It was suggested the patient see his MD immediately, and get back to us. Patient has not returned out call to let us know what tests, treatments, or outcomes he received.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Patient has not returned out call to let us know what tests, treatments, or outcomes he received.
- Aktuelle Erkrankungen
- UNKNOWN.
- Vorgeschichte
- UNKNOWN.
- Andere Medikamente
- UNKNOWN.
- Allergien
- NONE.
- Vorherige Impfungen
- -
- Staat
- ME
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Headache
Pain
Paraesthesia
Symptomtext
Patient contacted pharmacy on 1/14/22, she reported ongoing side effects following vaccination 9 days ago. She indicated that about 3 to 4 hours after her injection she started getting side effects that included significant headache and pain that radiated toward the neck and spine. This has continued. She indicated that she has had feelings of lightheadness and dizziness. She indicated that she has had feelings of tingling in all 4 extremities since the booster shot. Patient was calling to know more about what people have experienced and if it was a normal reaction and what would be next coarse of action. Rph indicated that since it was ongoing and of concern to patient that it was not getting better that rph would advise to be seen by medical provider
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- none at this time
- Aktuelle Erkrankungen
- asthma
- Vorgeschichte
- asthma
- Andere Medikamente
- unknown at this time
- Allergien
- endorsed allergies on consent form, exact details unknown at this time
- Vorherige Impfungen
- reports moderna reaction on dose 1 2/27/21 and dose 2 3/23/21 but not to this extent
- Staat
- FL
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Mobility decreased
Symptomtext
Patient reported experiencing loss of bodily movement after reaching home from her vaccination. (waited in-store 20 minutes after receiving vaccine). Pt has fully recovered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 08.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aphasia
Condition aggravated
Feeling abnormal
Memory impairment
Paraesthesia
Symptomtext
Both legs tingling like pins and needles. Brain fog. Neuro system not functioning like normal like I was on another planet. Having trouble remembering basic things and finding the right words when speaking. More forgetful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Zinc; Vitamin C and D
- Allergien
- -
- Vorherige Impfungen
- Tingling legs.
- Staat
- PR
- Alter
- 93,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Chest pain
Electrocardiogram
Tremor
Symptomtext
Patient reports having chest pain and involuntary tremors. Evaluation is carried out S/V. Patient is well oriented at this time of place and herself/person. A consultation with Doctor is made, which indicates that she remains under observation then contacted the ambulance to transport the patient to the nearest hospital. After evaluation of the ambulance staff. Vital signs are reassessed and an EKG is performed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n /a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest pain
Condition aggravated
Dyspnoea
Headache
Heart rate irregular
Palpitations
Symptomtext
By administering the third dose of the Moderna vaccine, everything was stable until 11 p.m. My heart started to beat harder, my heart started racing, I also started feeling chest pain in part the front of my chest and the back of the chest. Also I have difficulty breathing I have to breathe up to a certain limit because if it does not give me chest pain and headache
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- I have not attended no doctor.
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NONE
- Allergien
- NO
- Vorherige Impfungen
- Yes. I felt a racing heart, shortness of breath, chest pain in front and behind the chest and headache. She was 38 years old and
- Staat
- FL
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 21.02.2023
- Impfdatum
- 08.01.2022
- Beginn
- 30.01.2023
- Tage bis Beginn
- 387,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asymptomatic COVID-19
Dizziness
SARS-CoV-2 test positive
Vertigo
Symptomtext
Hospitalization: 1/30/2023 - 1/31/2023 (27 hours) Presentation to the ED: dizziness and vertigo symptoms concerning for possible CVA COVID + date: 1/30/2023 Treatment: ASYMPTOMATIC. NO TREATMENT REQUIRED. Discharge to: HOME. 006B21A 3/17/2021 037B21A 4/17/2021 001J212A 1/8/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- no significant past medical history
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 03.01.2023
- Impfdatum
- 21.12.2021
- Beginn
- 11.11.2022
- Tage bis Beginn
- 325,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Aphonia
COVID-19
Cough
Pyrexia
Respiratory tract congestion
SARS-CoV-2 test positive
Sneezing
Symptomtext
On November 11, 2022, my infection began with congestion and sneezing and coughing, but not a deep cough. I had a low-grade fever. By Sunday I started coughing more and the next day I was losing my voice because I was coughing so much. My fever increased by Tuesday and on Wednesday - Thursday my fever remained 102. I got Paxlovid on that Friday when I went to the urgent care. I tested positive on Wednesday for COVID-19. I still have a foggy memory and remain fatigued.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- Home COVID-19, positive, 11172022
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypothyroidism; Anxiety
- Andere Medikamente
- Synthroid; Spironolactone; Lexapro; Multi Vitamin
- Allergien
- Penicillin; Cats; Pine Trees
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 07.10.2022
- Impfdatum
- 07.01.2021
- Beginn
- 23.09.2022
- Tage bis Beginn
- 624,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Cough
Diarrhoea
Mental status changes
Nausea
SARS-CoV-2 test positive
Vomiting
Symptomtext
Hospitalization: 9/23/2022 - 9/27/2022. Presentation to the ED: AMS, COUGH, NAUSEA, VOMITING, DIARRHEA. COVID-19 + date: 9/23/22. Treatment: NO TREATMENT GIVEN SPECIFICALLY FOR COVID INFECTION. Discharge to: Home or Self Care.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, SMOKER, CHRONIC OPIOID USE.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 22.09.2022
- Impfdatum
- 06.04.2022
- Beginn
- 15.09.2022
- Tage bis Beginn
- 162,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Extra dose administered
Immunisation reaction
Injection site erythema
Injection site warmth
Malaise
SARS-CoV-2 test positive
Symptomtext
Patient had a series of 4 Covid vaccines with the last being on April 6, 2022 listed above. She recently developed symptomatic Covid (PCR confirmed) and within 24 hours of symptom onset developed a "Covid arm" on both the right and left previous injection sites. Pictures available if needed. The area on both arms was 2-3 inches in diameter red, warm and slightly indurated . The findings lasted 24 to 36 hours and there were no sequelae. She is not sure which shot time wise was given in each arm but the area involved was very distinctive and correspondent to the previous injection sites.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- lipitor multivitamins
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 65,0
- Geschlecht
- M
- Eingang
- 01.08.2022
- Impfdatum
- 21.01.2022
- Beginn
- 16.07.2022
- Tage bis Beginn
- 176,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
COVID-19
Fall
SARS-CoV-2 test positive
Symptomtext
7/16/2022 pt went to ER due to recent fall/back pain. Patient states he was diagnosed with Covid 7/11/2022 with a home Covid-19 testing kit. Denies c/o SOB, denies fever, denies N/V. Lives at home and takes Eliquis. Patient has been Covid + approximately 6 days. Pt tested Covid-19 + per PCR test at Hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 21.06.2022
- Impfdatum
- 19.03.2022
- Beginn
- 17.05.2022
- Tage bis Beginn
- 59,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
COVID-19
Chills
Fatigue
Feeling abnormal
Headache
Malaise
Oropharyngeal pain
Pyrexia
SARS-CoV-2 test positive
Symptomtext
I had 102 fever, terrible headache a sore throat with joint pain and chills. I felt like I had a foggy brain that lasted about two weeks. I was very fatigued. I took PAXLOVID, starting on May 17th 2022. I tested negative after 10 days. 5 days later my symptoms came back, I was not feeling perfect I tested positive again. I was sick for another week after that. I still have fatigue more than I have ever felt before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- COVID testing PCR - 05/2022.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Osteoarthritis
- Andere Medikamente
- Vitamin D; ONE A DAY vitamin; biotin; magnesium
- Allergien
- Penicillin; BACTRIM; tigecycline; kiwi; raw carrots
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 20.01.2021
- Beginn
- 27.01.2022
- Tage bis Beginn
- 372,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Chest discomfort
Chills
Computerised tomogram head normal
Fatigue
Head discomfort
Headache
Influenza like illness
Magnetic resonance imaging normal
Myalgia
Neck pain
Pain
Symptomtext
On 01/20/2022 at 5:00PM I experienced flu like symptoms of myalgia, chills, and fatigue that resolved at 4:00PM the next day. On 01/27/2022 at 7:00PM I experienced a dull ache of pain that went up the left side of my neck up into my head, the pressure in my head increased for a pounding painful pressure and headache that lasted intensely for 2 minutes before lessening to a dull pain again down the left side of my neck. There was also pressure on my rib cage in the center of my sternum, which lasted for an hour. The dull ache and pressure in my head lasted until I sought care in the ER and was administered pain medication. All of the symptoms resolved within about 24 hours and have not returned. I did not receive a diagnosis for my adverse event.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- CT Scan of the head on 01/27/2022 was clear MRI on 02/17/2022 was clear
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Vitamin D Fluoxetine 20mg Trazadone
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 11.05.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Biopsy
Granuloma annulare
Osteoarthritis
Pain in extremity
Symptomtext
The granuloma annulare continued to spread after the booster on my face, legs and arms. My dermatologist prescribed two steroid creams for relief. In February I experienced severe knee and leg pain. I went to see my doctor and was diagnosed with osteoarthritis.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Biopsy
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroid
- Andere Medikamente
- Levothyroxine Vitamin D2 Two Steroid Creams Clobetasol Propionate Desonide
- Allergien
- Penicillin Sulfa Drugs Naproxen
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 13.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abscess drainage
Anaemia
Bacterial infection
Blood glucose increased
Blood test abnormal
Chills
Erythema
Fatigue
Inflammation
Joint abscess
Joint swelling
Joint warmth
Pyrexia
Skin discolouration
Skin exfoliation
Symptomtext
01/13/2022 That evening after my vaccine, I noticed I had swelling in my knee. I had chills, was fatigued and had fever. I noticed inflammation of my nerve endings in my knee. It turned into a bacterial infection. I went to the doctor on 3/23/2022. By that time, it had swollen twice the size it should be. I had severe inflammation that was showing on the outside of the knee. Huge red discoloration and fever was noticed in the knee. My skin was also peeling off my knee. I went back to my doctor's office on 4/18/2022. I have been treated with antibiotics for 4 weeks for this infection. I am on the third round of antibiotics. The name of the antibiotics are Bactrim, Levaquin and Clindamycin. I am also taking over the counter probiotics my doctor told me to take. My knee has an abscess, it is draining and has improved. I had a knee replacement in 2016.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- Bloodwork, Glucose was a little high; Anemia
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Asthma; Diabetes Type II; High Blood Pressure
- Andere Medikamente
- Multivitamin for Women over 50 Vision Formula with Lutein Iron 81mg Aspirin Metformin Escitalopram Atorvastatin Levoxyl Montelukast Lisinopril Amlodipine Farxiga Glipizide
- Allergien
- Shellfish; Penicillin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 20.04.2022
- Impfdatum
- 18.03.2021
- Beginn
- 01.04.2021
- Tage bis Beginn
- 14,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Epistaxis
Exercise tolerance decreased
Fatigue
Headache
Influenza
Limb mass
Pain in extremity
Rash
Skin warm
Symptomtext
Upon receiving my first dose of Moderna, I developed a lump on my arm, severe pain in the arm and also a rash. I developed flu like symptoms with exception to the headache. The flue symptoms subsided in about 72 hours, the lump and rash and arm pain took about 7 days. After the second dose of Moderna, the arm pain was more severe, the rash was burning hot, and the lump was significantly larger and the flue symptoms were worse and one again after the flu symptoms and arm rash/lump/pain subsided the headache still remained. Over the past year, general fatigue has increased and the headache pain has increased. In December of 2021, along with the tiredness and headache, I also started getting nosebleeds. In February I sought medical help from my GP and have been placed indefinitely on migraine medication that comes with a whole list of side effects as well. I was once very active running every day and going to the gym regularly. I would normally run a half marathon a month and now I am lucky if I am able to get the energy to run once or twice a week and only a couple of miles.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- asthma
- Andere Medikamente
- Singulair Zyrtec Albuterol (when needed) Advair
- Allergien
- ammoxicillan seasonal
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 05.04.2022
- Impfdatum
- 02.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Mechanical urticaria
Urticaria
Symptomtext
Have been experiencing hives and dermatographia almost daily
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Oral contraceptives
- Allergien
- Allergic to penicillin
- Vorherige Impfungen
- Got hives from a penicillin shot (probably around age 5-7)
- Staat
- -
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 04.04.2022
- Impfdatum
- 17.03.2021
- Beginn
- 25.01.2022
- Tage bis Beginn
- 314,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
Fatigue
Laboratory test abnormal
Peripheral swelling
SARS-CoV-2 test positive
Symptomtext
01/25/22 presents to ED for "abnormal labs" "fatigue, leg swelling, and weakness" "recently was diagnosed is COVID positive". PMHx of "hypertension, Atrial fibrillation, GI bleed, colon ca,CKD"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- 01/25/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 01.04.2022
- 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: unbekannt
Chills
Dizziness
Nausea
Vision blurred
Symptomtext
DIZZY, NAUSEOUS, LIGHT HEADED, CHILLS, BLURRY VISION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Allergic to erythromycin, macro bid, amoxicillin, triazolam
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 17.01.2022
- Beginn
- 30.01.2022
- Tage bis Beginn
- 13,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
After receiving the vaccine, I had hives that appeared on my body about two weeks later. They appeared on my back mostly and spread out a little on my forehead and some of my arms. They went away after 24 hours, I took some Alka-Seltzer. I then saw the doctor who did a in office skin exam and determined it was hives. The hives still come and go and I take the over counter medication the doctor recommended.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- Kiwi, Raw pineapple
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 25.03.2022
- Beginn
- 26.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 7+
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site nodule
Injection site oedema
Injection site pain
Injection site warmth
Symptomtext
HARD KNOT, WARM TO TOUCH, RED, EDEMA AND PAIN AT INJECTION SITE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NO
- Andere Medikamente
- NA
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 28.03.2022
- Beginn
- 28.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Heart rate increased
Oropharyngeal pain
Pain
Pyrexia
Symptomtext
FEVER (101.8), INCREASED HEART RATE (124), HEADACHE, BODY ACHE, SORE THROAT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 25.03.2022
- Impfdatum
- 03.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 13,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Urticaria
Symptomtext
uncontrolled itching all over, followed by histamine reaction/ hives.. continuous since 2/16.... colleague with same exact symptoms, received 1 day apart from one another, from same facility, this was our booster shot, received 2 moderna vaccinations prior, asymptomatic for both.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- pcp visit on 3/7.... resulted in prednisone prescription, helped initially, now symptoms have returned.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- rosuvastatin calcium 5 mg. 81 mg asprin
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 17.03.2022
- Impfdatum
- 16.03.2022
- Beginn
- 16.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Chills
Headache
Myalgia
Nausea
Pyrexia
Symptomtext
FEVER, CHILLS, NAUSEA, HEADACHE, MUSCLE ACHES
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NO
- Vorgeschichte
- NO
- Andere Medikamente
- NO
- Allergien
- ALLERGY TO PENICILLIN
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 17.03.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Joint range of motion decreased
Pain
Pain in extremity
Symptomtext
Severe arm pain to touch or movement; restricted range of motion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Sulfa drugs Trazadone Contrast dye
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 58,0
- Geschlecht
- M
- Eingang
- 24.02.2022
- Impfdatum
- 14.07.1962
- Beginn
- 24.02.2022
- Tage bis Beginn
- 21.775,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Immediate post-injection reaction
Injection site pain
Injection site warmth
Symptomtext
BURNING IN THE INJECTION SITE (RIGHT DELTOID). PATIENT DESCRIBED AS HOT OR BURNING; USED SPILLING COFFEE ON YOURSELF AS AN EXAMPLE. STARTED IMMEDIATELY AFTER INJECTION. NO REDNESS OR SWELLING VISIBLE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- NONE. SELF REPORTED, NOT TESTS AVAILABLE FOR SYMPTOM EXPERIENCED.
- Aktuelle Erkrankungen
- None per patient
- Vorgeschichte
- None per patient
- Andere Medikamente
- Unknown, patient does not fill with administering pharmacy.
- Allergien
- None per patient
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Immediate post-injection reaction
Injection site hypoaesthesia
Product administered to patient of inappropriate age
No adverse event
Symptomtext
Patient was administered the first dose of the COVID vaccine series with Moderna (0.5 mL). The patient is 16 years old, and Moderna COVID vaccines are not approved for use in anyone less than 18 years of age at this time. No reported side effects. Unclear if barcoding technology was used and how vaccine was ordered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site hypoaesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CT
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 17.01.2022
- Beginn
- 27.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Erythema
Pruritus
Skin warm
Urticaria
Symptomtext
Presented with severe urticaria 10 days after booster. Redness, itchiness, swelling, warm to the touch - all over body from scalp to bottoms of feet. First visit to ER was given 2 steroid injections and prescribed Medrol dose pack and hydroxyzine for 6 days and Pepcid for 7 days. Symptoms kept calm but still itchy. 24 hours after finishing last prescription, hives came back again. Went back to the ER on 2/14 where I was prescribed prednisone for 10 days and Allegra 12 hour antihistamine. This course of treatment has helped better than the first but still have minor itchy from time to time. Currently done with prednisone but still taking Allegra and have an appointment with an allergist.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hyperlipidemia
- Andere Medikamente
- Atorvastatin 10mg PO QD
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- UT
- Alter
- 0,4
- Geschlecht
- F
- Eingang
- 20.02.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dermatitis diaper
Diarrhoea
Eczema
Exposure via breast milk
Inflammation
Irritability
Rash
Skin exfoliation
Symptomtext
This is to report an adverse reaction in my nursing baby. Starting the first afternoon after my vaccination, she broke out in a rash on her face and neck which later spread to her upper/middle trunk and also became a diaper rash. She was fussy and had loose bowels for 5-7 days. And bowel consistency still hasn?t returned to normal after 1 month. The rash is still here and will wax & wane and continue as I nurse her. Rash had a burn appearance initially and skin would open and peel. The rash sometimes looks like and behaves like exzema but also other times as the skin has healed, we see a spider-like capillary design under her almost healed skin which will then flare and erupt again. It appears to be an inflammatory response. Same baby had a similar reaction on a much much smaller scale after the first shot 28 days prior. (Dec. 20, 2021) We are still battling this 1 month later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Just seen our pediatrician And now an allergist/immunologist at a local hospital
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None known.
- Andere Medikamente
- None
- Allergien
- None known. Family history of food allergies.
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Symptomtext
Patient with dizziness after the booster vaccine. He consulted with Doctor who recommends that he make an appointment with his family doctor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Injection site induration
Injection site swelling
Symptomtext
Caregiver has reported symptoms of arm swelling/hardness at injection site that began on 1/14/22 post Covid-19 vaccine booster on 1/14/22 and worsened by 1/16/22. CG saw provider via Telehealth appointment, prescribed ABX for DX of Cellulitis and advised to apply warm compress to site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site induration
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 09.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Contusion
Oropharyngeal pain
Pain in extremity
Pruritus
Sinus congestion
Symptomtext
Sore arm, bruising, and intense itching on same side thigh, sore throat, congestion in sinuses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Oropharyngeal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- Intense anaphylactic flu shot reaction and respiratory infection.
- Staat
- PR
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 10.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Hyperhidrosis
Immediate post-injection reaction
Symptomtext
Patient reports dizziness and has profuse sweating. Alert and oriented x 3. Doctor is notified and remains under observation for 30 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Caltrate
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NE
- Alter
- 19,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 28.01.2022
- Beginn
- 03.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Rash
Symptomtext
Rash, lower lip swelling
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- ADHD
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 19,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 15.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pruritus
Rash
Urticaria
Symptomtext
Painful Rashes, itching, and hives all over body
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Adderall Syronx
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 28,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 25.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site infection
Symptomtext
Patient presented to her primary care clinic with an infection at the site of injection of her Covid-19 vaccine (Moderna) two days after her vaccination. Patient was prescribed Amoxicillin, Prednisone, and Hydrocodone/APAP by provider.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site infection
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- Salicylates, Sulfa Antibiotics
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Throat irritation
Symptomtext
Client vaccinated with first dose of Moderna without incident at 10:20 am. Had history of severe allergic reaction to bee sting as child. Instructed to stay for observation for 30 minutes. At 10:40 am reported itchy neck and feeling of "a ball in my throat". Monitored every 5 minutes for 90 minutes. Incident occurred at County Jail so jail staff gave him 50 mg Benadryl. O2 was 99%. At 11:35 client stated everything feels normal. Released back to POD at 12 noon.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Bee sting
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site rash
Rash
Symptomtext
Red rash on left bicep and outer arm above elbow. No pain. Started a week after injection and has persisted for the past week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site rash
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Parkinsons
- Andere Medikamente
- Unknown
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 31.01.2022
- Impfdatum
- 16.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asymptomatic COVID-19
Nausea
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Vomiting
Symptomtext
This is a 51-year-old female with a past medical history of anxiety, PE, seizure disorder, orthostatic hypotension, chronic pain, opiate dependency who presents to the emergency room for 3 days of intractable nausea and vomiting. Patient is asympomatic for COVID.Patient initially tested negative on 1/25/22 then turned positive 1/26/22. Previously received Moderna 3/31/21, 4/28/21 & 1/16/22. Discharged 1/28/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- 4,0
- Labordaten
- COVID 19 PCR + 1/26/22.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Anxiety; PE; Seizure disorder; Hypotension; Chronic pain.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 27.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Eye swelling
Peripheral swelling
Swelling
Urticaria
Symptomtext
Severe hives starting 10 days after shot. No known allergies. Going on now for a week and still severe. 13 days after shot eyes, head, feet, and hands swelled up, went to ER. Prescribed me steroids and antihistamines which don?t seem to help much
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 29,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Body temperature increased
Feeling hot
Malaise
Thirst
Symptomtext
approximately 6 hours after the booster (around 3pm) he felt ill. at 7:30 pm his temperature was 99.6, he took two 500 mg of tylenol and went to bed. at 3:30 am he was still feeling ill and still felt warm didn't check his temp with a thermometer however. He took two more 500 mg of tylenol and went back to bed. went back to bed after taking the tylenol and slept until 1pm the next day (today 1-21-2022). He was thirsty but said he felt some better. didn't take any tylenol but did drink some water. he asked me for more tylenol at 2:20 pm i checked his temperature with a forehead scanning thermometer, his temp was 102.4
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Schitzophrenia
- Andere Medikamente
- Perphenazine 24 mg at bedtime Rosuvastatin Calcium 20 mg at bedtime Benztropine MES 0.5 mg tab two tabs at bedtime Sertraline HCL 50 mg tab one at bedtime Olanzapine 30 mg at bedtime
- Allergien
- Sulpha
- Vorherige Impfungen
- both the first and second dose gave him a fever and he felt ill for a couple of days afterwards. recieived the first moderna on
- Staat
- MN
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Axillary pain
Injection site pain
Myalgia
Vascular pain
Symptomtext
Injection site pain on left arm, Pain near the left armpit, Muscle pain, Joint pain, Feeling like pain inside veins
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Acetaminophen 500mg, Baclofen 10 mg, Cholecalciferol 2000 IU
- Allergien
- Dust allergy
- Vorherige Impfungen
- Injection site pain, Fever and Chill; 35 years old; 04/01/2021 and 04/28/2021; COVID-19 Vaccine; Moderna
- Staat
- KY
- Alter
- 24,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysphagia
Ear swelling
Erythema
Pruritus
Skin swelling
Skin warm
Symptomtext
Patient states difficulty swallowing, itching skin with red puffy areas and swollen, ears swollen and hot to the touch
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N?A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Unknown
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Dizziness
Headache
Immediate post-injection reaction
Pallor
Symptomtext
The recipient felt dizzy, had a headache, and was very pale immediately following receiving the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Unknown
- Aktuelle Erkrankungen
- Uknown
- Vorgeschichte
- Unkown
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Rash pruritic
Symptomtext
ON 1/18/22 PATIENT CAME TO PHARMACY TO REPORT ITCHY RASH ON BOTH PALMS OF HANDS AND SOLES OF BOTH FEET THAT STARTED ON 1/16/22. SHE REPORTS SHE WAS SEEN BY A PHYSICIAN AND EVALUATED ON 1/18/22. NO TREATMENT WAS PRESCRIBED AND PER PATIENT SHE WAS ADVISED BY THE PHYSICIAN TO GO AHEAD WITH HER SECOND DOSE OF THE COVID VACCINE. PATIENT CAME IN TO PHARMACY TO REPORT THE EVENT PER INSTRUCTIONS IN ORDER FOR THE PHARMACY TO DOCUMENT AND REPORT THE ADVERSE EVENT. PATIENT WAS GIVEN AND INSTRUCTED BY THIS PHARMACIST INFORMATION ON SELF- REPORTING TO V-SAFE AND TO MODERNA THE EVENT WHICH OCCURED TO HER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 6,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Rash pruritic
Symptomtext
ON 1/18/22 PATIENT CAME TO PHARMACY TO REPORT ITCHY RASH ON BOTH PALMS OF HANDS AND SOLES OF BOTH FEET THAT STARTED ON 1/16/22. SHE REPORTS SHE WAS SEEN BY A PHYSICIAN AND EVALUATED ON 1/18/22. NO TREATMENT WAS PRESCRIBED AND PER PATIENT SHE WAS ADVISED BY THE PHYSICIAN TO GO AHEAD WITH HER SECOND DOSE OF THE COVID VACCINE. PATIENT CAME IN TO PHARMACY TO REPORT THE EVENT PER INSTRUCTIONS IN ORDER FOR THE PHARMACY TO DOCUMENT AND REPORT THE ADVERSE EVENT. PATIENT WAS GIVEN AND INSTRUCTED BY THIS PHARMACIST INFORMATION ON SELF- REPORTING TO V-SAFE AND TO MODERNA THE EVENT WHICH OCCURED TO HER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Feeling hot
Nausea
Symptomtext
Patient felt hot, dizzy and nauseated about 10 minutes after receiving Moderna booster vaccine. She did not appear anxious or nervous at the time of vaccination. She tolerated the first and second vaccines well. She appears to be ok now.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 10.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Dysphonia
Headache
Pain
SARS-CoV-2 test positive
Symptomtext
Woke up at night because of ache and pain, severe headache, coughing and hoarseness. Later in the day increasingly so throughout the day. My temp is usually low but it showed 99.0? as opposed to my usual 97.6. Was advised to take an at home COVID test and showed positive that day.(1/13) Appointment scheduled for 1/17 at 10:30 CT. No contact with Medical Professional. Have been using a Proventil that was given to me during my last COVID infection. Also, been taking a Daytime Cold relief pill.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 1/13 COVID Rapid (Positive).
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Environmental Allergies, UCTD. Sicca syndrome, Raynaud's syndrome, Carpal tunnel (both wrist), Hidradenitis suppurativa
- Andere Medikamente
- Trazodone; Temazepam; Gabapentin; Clonazepam; Protonix; Plaquenil; Dayzie; Minocin; Clinoril; Restasis; Claritin; Biotin; Vitamin C; D3; Zinc; Acidophilus; Prenatal MultiVitamin; Magnesium; Omega 3
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 08.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Confusional state
Fall
General physical condition abnormal
Malaise
Mydriasis
Somnolence
Symptomtext
WEAKNESS AND CONFUSION, SLEEPINESS, DIALTAED EYES, "LOOKING HIGH" ACCORDING TO WIFE AND DAUGHTER. PARAMEDICS CALLED TO HELP LIFT PATIENT FROM THE FLOOR AS WIFE COULD NOT. PARAMEDICS TOOK PATIENT VITALS AND STATED THAT THEY WERE NORMAL. PATIENT WAS NOT TRANSPORTED AND PARAMEDICS FELT HE WOULD BE FINE AT HOME. PATIENT STILL HAVING MALAISE DAYS LATER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- PARAMEDICS TOOK PATIENT VITALS 1/9/2022 AND STATED THEY WERE NORMAL.
- Aktuelle Erkrankungen
- DIABETIES, DECREASED PULMONARY FUNCTION
- Vorgeschichte
- DIABETES, DECREASED PULMONARY FUNCTION
- Andere Medikamente
- METFORMIN 1000MG TAB, JARDIANCE 25MG TAB, ATORVASTATIN 40MG TAB, BREO ELLIPTA 100-25 INH, METOPROLOL ER 100MG TAB, PROVENTIL HFA , GLYBURIDE 5MG TAB, TRULICITY 1.5/0.5 INJ, ELIQUIS 5MG TAB
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 13.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 13.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Malaise
Unresponsive to stimuli
Symptomtext
Patient received the Moderna vaccine at 4pm on Wednesday 01/12/22 at 4 pm. No complications were reported after the vaccine was administered. Patient did not report any symptoms prior to going to bed. Patient awoke feeling unwell around 6-7am on 01/13/22 and was given two tylenols from Wife to help with symptoms. They then request to move to the bathroom where thereafter they were found on the ground and unresponsive. Emergency response was called shortly afterwards.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Malaise
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 13.01.2022
- Impfdatum
- 03.06.2021
- Beginn
- 10.01.2022
- Tage bis Beginn
- 221,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Back pain
Dizziness
Feeling abnormal
Headache
Hypersomnia
Impaired work ability
Nausea
Neck pain
Symptomtext
Since I have received my booster shot on Sunday January 10,2022, I would like you to know that Monday January 11th I came home from work I have slept until Wednesday morning. when the 12 2022. I have called my doctor I went in to see him this Morning at 8 am January 13,2022. Symptoms are lower back pain, dizziness, head pain neck pain and also nausea. He game Ondansetron HCL. Also, Ibuprofen 800 mg tab for pain I am out of my 2 jobs work until Monday January 17th I can go back. I am having a real bad time with this shot I have received the Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- No.
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- No.
- Andere Medikamente
- No.
- Allergien
- Procardia XL30.
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 07.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Fatigue
Myalgia
Nausea
Pyrexia
Symptomtext
Pt. states that after receiving the 3rd dose of Moderna 01/07/2022, started experiencing symptoms that evening of fever (101.7 lasting 01/11/2022), chills, muscle aches, fatigue, and nausea. No noted Primary visit/communications. Symptoms have subsided after 72hrs.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- HBP
- Andere Medikamente
- Atenolol, Losartan, Amlodipine, Omeprazole, Baby Aspirin
- Allergien
- Pennicillin
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 90,0
- Geschlecht
- F
- Eingang
- 18.09.2023
- Impfdatum
- 13.02.2023
- Beginn
- 13.02.2023
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- Desconocido
- Aktuelle Erkrankungen
- Alzheimer's.
- Vorgeschichte
- Alzheimer's.
- Andere Medikamente
- Unknown.
- Allergien
- Unknown.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 14.03.2023
- Impfdatum
- 07.09.2022
- Beginn
- 07.09.2022
- 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
Wrong product administered
Symptomtext
No adverse event; The vaccine received on 07-Sep-2022 with lot number 001J21-2A was expired on 12-Apr-2022 long before Moderna bivalent vaccine was available.; Patients thought they received Moderna bivalent vaccine booster dose however it was monovalent with lot number 001J21-2A which was expired.; This spontaneous case was reported by a consumer and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The vaccine received on 07-Sep-2022 with lot number 001J21-2A was expired on 12-Apr-2022 long before Moderna bivalent vaccine was available.), WRONG PRODUCT ADMINISTERED (Patients thought they received Moderna bivalent vaccine booster dose however it was monovalent with lot number 001J21-2A which was expired.) and NO ADVERSE EVENT (No adverse event) in a 50-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J21-2A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: PFIZER BIONTECH COVID-19 VACCINE. Past adverse reactions to the above products included No adverse reaction with PFIZER BIONTECH COVID-19 VACCINE. On 07-Sep-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 07-Sep-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The vaccine received on 07-Sep-2022 with lot number 001J21-2A was expired on 12-Apr-2022 long before Moderna bivalent vaccine was available.) and WRONG PRODUCT ADMINISTERED (Patients thought they received Moderna bivalent vaccine booster dose however it was monovalent with lot number 001J21-2A which was expired.). On an unknown date, the patient experienced NO ADVERSE EVENT (No adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The vaccine received on 07-Sep-2022 with lot number 001J21-2A was expired on 12-Apr-2022 long before Moderna bivalent vaccine was available.), WRONG PRODUCT ADMINISTERED (Patients thought they received Moderna bivalent vaccine booster dose however it was monovalent with lot number 001J21-2A which was expired.) and NO ADVERSE EVENT (No adverse event) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be related. No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (The vaccine received on 07-Sep-2022 with lot number 001J21-2A was expired on 12-Apr-2022 long before Moderna bivalent vaccine was available.) and WRONG PRODUCT ADMINISTERED (Patients thought they received Moderna bivalent vaccine booster dose however it was monovalent with lot number 001J21-2A which was expired.). No concomitant medications were reported. The reporter reported that his wife also received expired Moderna Covid-19 monovalent vaccine instead of Moderna Bivalent vaccine on 07-Sep-2022. The reporter and his wife went to pharmacy to check if they received Moderna bivalent booster dose on 07-Sep-2022. The vaccine received on 07-Sep-2022 with lot number 001J21-2A was expired on 12-Apr-2022 long before Moderna bivalent vaccine was available. On 07-Sep-2022 the patients had traveled to an unfamiliar part of town to eat at a highly regarded Taco restaurant. After that they ventured to the building next sore which had a tent and a Health Care Professional offering to give the patient and his wife updated Moderna bivalent booster shots. Patients thought they received Moderna bivalent vaccine booster dose however it was monovalent with lot number 001J21-2A which was expired. The caller reports that his wife received Pfizer vaccine for all her Previous Covid-19 vaccines prior to the Moderna booster dose on 07-Sep-2022. No treatment information was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 26.10.2022
- Impfdatum
- 28.01.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Burning sensation
Hot flush
Influenza like illness
Lymphadenopathy
Symptomtext
face burn just a little bit; had minor flu like symptoms; Lymph nodes swell up; hot flashes increase in number; This spontaneous case was reported by a patient and describes the occurrence of BURNING SENSATION (face burn just a little bit), INFLUENZA LIKE ILLNESS (had minor flu like symptoms), HOT FLUSH (hot flashes increase in number) and LYMPHADENOPATHY (Lymph nodes swell up) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J212A) for COVID-19 prophylaxis. Patient had no history of COVID positive test or diagnosis. Patient had no history relating to mentioned AE and both Acute and Chronic illnesses at the time of vaccination. Patient did not receive any other vaccines given within 1 month prior to Moderna COVID-19 vaccine. Concurrent medical conditions included Gluten intolerance, Soy allergy, Allergy to nuts (tree nuts), Peanut allergy, Vegetable allergy (tomatoes), Allergy to chemicals (coloring dyes), Egg allergy, Sesame allergy, Shellfish allergy, Drug allergy (Oxycodone) and Postmenopause. Concomitant products included ETHINYLESTRADIOL, NORETHISTERONE ACETATE (MICROGESTIN) and LEVOTHYROXINE SODIUM (TIROSINT) for an unknown indication. On 28-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On an unknown date, the patient experienced BURNING SENSATION (face burn just a little bit), INFLUENZA LIKE ILLNESS (had minor flu like symptoms), HOT FLUSH (hot flashes increase in number) and LYMPHADENOPATHY (Lymph nodes swell up). At the time of the report, BURNING SENSATION (face burn just a little bit) and LYMPHADENOPATHY (Lymph nodes swell up) outcome was unknown and INFLUENZA LIKE ILLNESS (had minor flu like symptoms) and HOT FLUSH (hot flashes increase in number) had resolved. Patient had received Moderna vaccine 1st dose on 14Apr2021, left arm IM with lot no 040B21A and 2nd dose on 12May2022 left arm IM with lot no 014C21A. Patient received half dose of 1st booster in left arm (a little higher up in the muscle). Patient had minor flu like symptoms for a day and half. Patient experienced hot flashes increased in number and had severity for 4 months. No treatment information was provided by the reporter. This case was linked to MOD-2022-662107, MOD-2022-662027 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Burning sensation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy to chemicals (coloring dyes); Allergy to nuts (tree nuts); Drug allergy (Oxycodone); Egg allergy; Gluten intolerance; Peanut allergy; Postmenopause; Sesame allergy; Shellfish allergy; Soy allergy; Vegetable allergy (tomatoes)
- Vorgeschichte
- Comments: Patient had no history of COVID positive test or diagnosis. Patient had no history relating to mentioned AE and both Acute and Chronic illnesses at the time of vaccination. Patient did not receive any other vaccines given within 1 month prior to Moderna COVID-19 vaccine.
- Andere Medikamente
- MICROGESTIN; TIROSINT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 08.09.2022
- Impfdatum
- 24.03.2021
- Beginn
- 24.08.2022
- Tage bis Beginn
- 518,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Heart rate increased
Imaging procedure abnormal
Symptomtext
08/24/22 presents to EC ED for "abnormal imaging and rapid heart rate". PMHx of "Ischemic stroke L parietal lobe with small superimposed hemorrhage 07/22, Afib, IDDM s/p RBKA and L toe amputation, HTN, HLD, PVD "
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate increased
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 11.08.2022
- Impfdatum
- 09.01.2022
- Beginn
- 01.08.2022
- Tage bis Beginn
- 204,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asymptomatic COVID-19
SARS-CoV-2 test positive
Thrombocytopenia
Transfusion
Symptomtext
Patient was admitted to hospital for thrombocytopenia, treated with transfusions. Upon discharging pt tested + for covid asymptomatic.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asymptomatic COVID-19
- Hospital-Tage
- 11,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- BPH Copd Gerd osteoarthritis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 11.08.2022
- Impfdatum
- 21.01.2022
- Beginn
- 26.05.2022
- Tage bis Beginn
- 125,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Product storage error
SARS-CoV-2 test
Symptomtext
This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after expiration date), PRODUCT STORAGE ERROR (Vial was expired on 13-May-2022, stored in refrigerator on 21-Jan-2022 and administered on 26-May-2022) and NO ADVERSE EVENT (no adverse event) in a 60-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 003K21-2A and 001J21-2A) for COVID-19 prophylaxis. It was unknown if patient had acute illnesses at the time of vaccination and up to one month before. It was unknown if patient had chronic or long-standing health conditions. Previously administered products included for Product used for unknown indication: Pfizer / BioNTech (Dose number: 1, Batch/lot number- EW0186, 0.3 milliliter, Route of administration- intramuscular, left arm.) on 24-May-2021, Pfizer / BioNTech (Dose number- 2, Batch/lot number- EW0180, 0.3 milliliter, Route of administration- intramuscular and left arm.) on 14-Jun-2021. Past adverse reactions to the above products included No adverse event with Pfizer / BioNTech and Pfizer / BioNTech. On 21-Jan-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .25 milliliter. On 26-May-2022 at 9:24 AM, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) dosage was changed to .25 milliliter. On 26-May-2022 at 9:24 AM, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after expiration date). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vial was expired on 13-May-2022, stored in refrigerator on 21-Jan-2022 and administered on 26-May-2022) and NO ADVERSE EVENT (no adverse event). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after expiration date), PRODUCT STORAGE ERROR (Vial was expired on 13-May-2022, stored in refrigerator on 21-Jan-2022 and administered on 26-May-2022) and NO ADVERSE EVENT (no adverse event) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, SARS-CoV-2 test: (Positive) Positive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter considered NO ADVERSE EVENT (no adverse event) to be not related and EXPIRED PRODUCT ADMINISTERED (Dose administered after expiration date) and PRODUCT STORAGE ERROR (Vial was expired on 13-May-2022, stored in refrigerator on 21-Jan-2022 and administered on 26-May-2022) to have an unknown relationship. It was unknown if any prescriptions, over-the-counter-medications, dietary supplements, or herbal remedies were being taken by the patient at the time of vaccination and/or at the time of the adverse event. No treatment medications was provided by the reporter. The used vials were placed in the refrigerator on the same day of administration 26-May-2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 test; Test Result: Positive; Result Unstructured Data: Positive.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Comments: It was unknown if patient had acute illnesses at the time of vaccination and up to one month before. It was unknown if patient had chronic or long-standing health conditions.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 21.07.2022
- Impfdatum
- 20.01.2022
- Beginn
- 23.06.2022
- Tage bis Beginn
- 154,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
Breakthrough Case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Covid + on 06/23/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 31.12.2021
- Beginn
- 18.07.2022
- Tage bis Beginn
- 199,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Exposure to SARS-CoV-2
Fall
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Symptomtext
Pt presented to ER post ground level fall. He also was positive for COVID and reported that he has had a runny nose and congested for about a week and was exposed to his brother who was positive for COVID.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 13.07.2022
- Impfdatum
- 11.01.2022
- Beginn
- 01.04.2022
- Tage bis Beginn
- 80,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Macular hole
Symptomtext
After the 3rd dose I had a Macular hole on my right eye. I was given eye drops to see if it will help heal. I'm currently waiting for surgery to fix it
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Macular hole
- Hospital-Tage
- -
- Labordaten
- Eye exam - Macular hole condition
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Long-term depression and anxiety; Anemia; Blood clot
- Andere Medikamente
- Warfarin; Omeprazole; Wellbutrin
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 19.01.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 19,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Tinnitus
Symptomtext
I am prone to tinnitus but now it seems to be constant ringing in both ears and it doesn't stop. It seems to have gotten worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tinnitus
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None
- Andere Medikamente
- Fish Oil; Iron Supplement; Vitamin D; Hydrochlorothiazide
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 91,0
- Geschlecht
- M
- Eingang
- 29.04.2022
- Impfdatum
- 05.01.2022
- Beginn
- 24.04.2022
- Tage bis Beginn
- 109,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- RI
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 10.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 5,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Atrial fibrillation
Blood electrolytes
Chest discomfort
Electrocardiogram
Symptomtext
4/15/2022: Treated at Hospital ER for: Chest Discomfort, Rapid Afib with RVR. Arrived to ER vis Rescue at 810pm and discharged home at 1145pm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Atrial fibrillation
- Hospital-Tage
- -
- Labordaten
- EKG, Electrolytes
- Aktuelle Erkrankungen
- Sinus Infection.
- Vorgeschichte
- Sinusitis
- Andere Medikamente
- Omega3 500mg one gel tab daily. Vision Formula+50 one gel tab daily. Fexofenadine 180mg one tablet daily. Famotadine 20mg one tablet daily, Guaiafenesin 600mg-Dextromethorphan tablet 2-3x daily.
- Allergien
- PenVK Sulfa Patanol eye drops Latex Kiwi, Nuts
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 14.04.2022
- Beginn
- 14.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Dose administered after manufacturer date of expiry; The vial first expired on 12-Apr-2022 and was then stored in the refrigerator on 14-Apr-2022; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) and PRODUCT STORAGE ERROR (The vial first expired on 12-Apr-2022 and was then stored in the refrigerator on 14-Apr-2022) in a 37-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 14-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) and PRODUCT STORAGE ERROR (The vial first expired on 12-Apr-2022 and was then stored in the refrigerator on 14-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered after manufacturer date of expiry) and PRODUCT STORAGE ERROR (The vial first expired on 12-Apr-2022 and was then stored in the refrigerator on 14-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment information was reported. The patient had received the second booster dose of the vaccine. It was reported that the vial had not undergone any temperature excursion issues. The reporter asked about what plan of action needs to be taken for the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- -
- Geschlecht
- U
- Eingang
- 20.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Gave 3 booster doses of Lot # that expired on the 12Apr2022.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Gave 3 booster doses of Lot # that expired on the 12Apr2022.) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 15-Apr-2022, the patient received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Gave 3 booster doses of Lot # that expired on the 12Apr2022.). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Gave 3 booster doses of Lot # that expired on the 12Apr2022.) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication reported. No treatment medication reported. The reporter stated that they were administering Moderna COVID-19 vaccines and stated that they gave 3 booster doses that expired on the 12 Apr 2022. The HCP was unable to provide any additional details about the patients except that it was their 2nd booster dose. On 08 Apr 2022 the vial was initially stored in the refrigerator. Reporter did not allow further contact
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 19.04.2022
- Impfdatum
- 13.04.2022
- Beginn
- 13.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Vaccine expired on 12-Apr-2022 was initially stored in refrigerator on 13-Apr-2022; A patient was administered an expired dose; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (A patient was administered an expired dose) and PRODUCT STORAGE ERROR (Vaccine expired on 12-Apr-2022 was initially stored in refrigerator on 13-Apr-2022) in a 68-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J21-2a) for COVID-19 vaccination. No Medical History information was reported. On 13-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 13-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (A patient was administered an expired dose). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine expired on 12-Apr-2022 was initially stored in refrigerator on 13-Apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (A patient was administered an expired dose) and PRODUCT STORAGE ERROR (Vaccine expired on 12-Apr-2022 was initially stored in refrigerator on 13-Apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication was reported. It was reported that the patient was administered with the 2nd booster dose on 13-Apr-2022. Date the vial was initially stored in the refrigerator was on 13-Apr-2022. The vial did not undergo any temperature excursions. Patient did not experience any symptoms. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 13-Apr-2022: Follow-up document received includes no new information.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 15.04.2022
- Impfdatum
- 28.03.2022
- Beginn
- 29.03.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Angiopathy
Eye disorder
Symptomtext
Patient states she had vascular event following the vaccine administration. Reports ocular changes. Patient followed up with hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Angiopathy
- Hospital-Tage
- -
- Labordaten
- unknown
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- thyroid issues, celiac disease, arthritis, gout, idiopathic leg edema
- Andere Medikamente
- Alprazolam, spironolactone, febuxostat, hydroxychlorquine, loratidine, liothyronine, torsemide, vitamin d 2000
- Allergien
- Seafood, all nuts, stone fruits
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 15.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
pt was given vaccine that expired on 4/12/2022 and it was administered 4/15/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 15.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
pt was given vaccine that expired on 4/12/2022 and it was administered 4/15/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 15.04.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- 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
Expired vaccine given. 04/12/2022 was expiration date for vaccine but was administered on 4/15/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 06.04.2022
- Impfdatum
- 26.01.2022
- Beginn
- 04.03.2022
- Tage bis Beginn
- 37,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Acute left ventricular failure
Cardiac failure congestive
Catheterisation cardiac abnormal
Coronary artery disease
Delusion of parasitosis
Symptomtext
ED visit for delusions of parasitosis. Treated and released. ED to hospital visit 6 days later for Acute systolic congestive heart failure. Cardiac Catheterization completed 3/9: Left and right heart cath showed moderate non-obstructive coronary artery disease with normal filling pressures. Per Cardiology recommendation: -Start Crestor 20 mg daily -Start Aspirin 81 mg daily ED visits and hospital admission within 6 weeks of receiving the COVID vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute left ventricular failure
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 24,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 08.02.2022
- Beginn
- 12.02.2022
- Tage bis Beginn
- 4,0
- Dosis
- 1
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Abscess
Appendicitis
Appendicitis perforated
Exposure during pregnancy
Focal peritonitis
Infection
Symptomtext
Acute appendicitis with perforation, localized peritonitis and abscess. Patient continued on antibiotics post-op given perforation with abscess. Her diet advanced. She was ready for discharge. ED visit to hospital admission at 8 weeks pregnant; 6 weeks within receiving the COVID-19 vaccine. Re-admitted 2/18/2022 for infection. Treated and discharged. EDD unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abscess
- Hospital-Tage
- 6,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 27.03.2022
- Beginn
- 27.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
Dose administered out a vial that experienced excursion for 4 hours; Dose administered out a vial that experienced excursion for 4 hours; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Dose administered out a vial that experienced excursion for 4 hours) and POOR QUALITY PRODUCT ADMINISTERED (Dose administered out a vial that experienced excursion for 4 hours) in a 36-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 27-Mar-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 27-Mar-2022, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (Dose administered out a vial that experienced excursion for 4 hours). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Dose administered out a vial that experienced excursion for 4 hours). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Dose administered out a vial that experienced excursion for 4 hours) and POOR QUALITY PRODUCT ADMINISTERED (Dose administered out a vial that experienced excursion for 4 hours) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medications were not provided. Treatment information was not reported. The vials were returned to stable temperature of refrigerator after 4 hours. The patient received the booster dose. This case was linked to MOD-2022-525790, MOD-2022-525469 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 31.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- 27.03.2022
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
Doses administered out a vial which experienced excursion for 4 hours; Doses administered out a vial which experienced excursion for 4 hours; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Doses administered out a vial which experienced excursion for 4 hours) and POOR QUALITY PRODUCT ADMINISTERED (Doses administered out a vial which experienced excursion for 4 hours) in a 30-year-old male patient who received mRNA-1273 (Spikevax) (batch nos. 001J21-2A and 001J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 27-Feb-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 27-Mar-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 27-Mar-2022, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (Doses administered out a vial which experienced excursion for 4 hours). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Doses administered out a vial which experienced excursion for 4 hours). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Doses administered out a vial which experienced excursion for 4 hours) and POOR QUALITY PRODUCT ADMINISTERED (Doses administered out a vial which experienced excursion for 4 hours) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. No treatment information was reported. The vials were returned to stable refrigerator temperature after 4 hours. This case was linked to MOD-2022-525469, MOD-2022-525791 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 31.03.2022
- Impfdatum
- 27.02.2022
- Beginn
- 27.03.2022
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Poor quality product administered
Product temperature excursion issue
Symptomtext
Doses administered out a vial that experienced excursion for 4 hours; Doses administered out a vial that experienced excursion; This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT TEMPERATURE EXCURSION ISSUE (Doses administered out a vial that experienced excursion for 4 hours) and POOR QUALITY PRODUCT ADMINISTERED (Doses administered out a vial that experienced excursion) in a 32-year-old female patient who received mRNA-1273 (Spikevax) (batch nos. 001J21-2A and 001J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 27-Feb-2022, the patient received first dose of mRNA-1273 (Spikevax) (unknown route) 1 dosage form. On 27-Mar-2022, received second dose of mRNA-1273 (Spikevax) (unknown route) dosage was changed to 1 dosage form. On 27-Mar-2022, the patient experienced POOR QUALITY PRODUCT ADMINISTERED (Doses administered out a vial that experienced excursion). On an unknown date, the patient experienced PRODUCT TEMPERATURE EXCURSION ISSUE (Doses administered out a vial that experienced excursion for 4 hours). At the time of the report, PRODUCT TEMPERATURE EXCURSION ISSUE (Doses administered out a vial that experienced excursion for 4 hours) and POOR QUALITY PRODUCT ADMINISTERED (Doses administered out a vial that experienced excursion) outcome was unknown. For mRNA-1273 (Spikevax) (Unknown), the reporter did not provide any causality assessments. No concomitant medication information provided. It was reported that 3 doses were administered out a vial which experienced excursion for 4 hours. The vials were returned to stable refrigerator temperature after 4 hours. No treatment information provided This case was linked to MOD-2022-525790, MOD-2022-525791 (Patient Link).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Poor quality product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 23.03.2022
- Impfdatum
- 23.03.2022
- Beginn
- 23.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient received the Moderna COVID-19 vaccine instead of the Pfizer COVID-19 vaccine based on his age
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
There was no adverse reaction, vaccine was administered on 02/23/22 and vaccine expired on 02/17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
There was no adverse reaction, vaccine was administered on 02/23/22 and vaccine expired on 02/17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 39,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
There was no adverse reaction, vaccine was administered on 02/23/22 and vaccine expired on 02/17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 98,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
There was no adverse reaction, vaccine was administered on 02/23/22 and vaccine expired on 02/17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
There was no adverse reaction, vaccine was administered on 02/23/22 and vaccine expired on 02/17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
There was no adverse reaction, vaccine was administered on 02/23/22 and vaccine expired on 02/17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
There was no adverse reaction, vaccine was administered on 02/23/22 and vaccine expired on 02/17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
There was no adverse reaction, vaccine was administered on 02/23/22 and vaccine expired on 02/17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
There was no adverse reaction, vaccine was administered on 02/23/22 and vaccine expired on 02/17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
There was no adverse reaction, vaccine was administered on 02/23/22 and vaccine expired on 02/17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
There was no adverse reaction, vaccine was administered on 02/23/22 and vaccine expired on 02/17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
There was no allergic reaction, PT was vaccinated on 02/23/22, vaccine expired on 02/17/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
No adverse effect, PT was vaccinated 02/23/22, Vaccine expired 02/17/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 18.03.2022
- 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: unbekannt
Expired product administered
No adverse event
Symptomtext
There was no adverse effect, vaccine was administered on February 23, vaccine has expiration dose on February 17.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 17,0
- Geschlecht
- M
- Eingang
- 13.03.2022
- Impfdatum
- 10.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient is 17 years old but received Moderna that is indicated for 18 years and older.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 10.03.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- 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
No adverse event
Symptomtext
Patient received full 0.5 ml dose of Moderna in error after previously receiving doses of Pfizer on 2/6/21 and 2/27/21 and a Moderna Booster (0.25ml) on 11/26/21 No known adverse reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- -
- Geschlecht
- M
- Eingang
- 07.03.2022
- Impfdatum
- 07.03.2022
- Beginn
- 07.03.2022
- Tage bis Beginn
- 0,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
No adverse event
Symptomtext
Patient received her initial Moderna series at Pharmacy on 04/30/2021 (0.5mL), and 05/28/2021 (0.5mL). She later received her booster (0.25mL) at Primary care on 12/16/2021. This booster dose was not inputted. Patient came into office today to receive a Moderna booster. Nurse checked , which advised nurse to administer booster today without knowing patient had already received Moderna booster (0.25mL) on 12/16/21. Moderna 0.25mL booster was given today. This was her 4th dose of Moderna. No adverse reaction/event occurred. However, Pharmacists recommend to report additional 4th dose to VAERS.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Type 2 diabetes mellitus without complication, sleep apnea, hypothyroidism, hypertensive disorder, hyperlipidemia, elevated liver enzymes level, depressive disorder, body mass index 40+ - severely obese, anxiety.
- Andere Medikamente
- Buspirone; Dextroamphetamine-amphetamine; Duloxetine; Euthyrox; Farxiga; Ibuprofen; Metformin; Olanzapine; Ozempic; Propranolol; Topiramate.
- Allergien
- Oxycodone.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 27.02.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong product administered
Symptomtext
Patient booked an appointment and requested the booster shot of the Janssen vaccine. However, the wrong vaccine was administered. Patient was given the booster dose (0.25ml) of Moderna. No adverse reaction was observed after the shot during the patient's stay in the pharmacy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- NA
- Vorgeschichte
- NA
- Andere Medikamente
- None on file at the time
- Allergien
- NA
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 26.02.2022
- Impfdatum
- 26.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
This spontaneous case reported by an other healthcare professional, describes the occurrence of product administered to patient of inappropriate age (received a Moderna vaccination while under the age of 18) in a 16-year-old male patient who received mRNA-1273 (Moderna COVID-19 vaccine, batch/lot# 001J212A) for COVID-19 immunization. No medical history reported. On Jan 26, 2022, patient received a dose of mRNA-1273 (Moderna COVID-19 vaccine), unknown route; 1 dosage form. On Jan 26, 2022, product administered to patient of inappropriate age (received a Moderna vaccination while under the age of 18). At the time of the report, product administered to patient of inappropriate age (received a Moderna vaccination while under the age of 18) outcome: unknown. The reporter did not provide any causality assessments, concomitant medication or treatment information. Reportedly, patient had no side effect after vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 61,0
- Geschlecht
- M
- Eingang
- 24.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- 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
Medication error
Symptomtext
MEDICATION ERROR - GAVE 0.5 ML INSTEAD OF THE 0.25 ML THAT SHOULD HAVE BEEN GIVEN FOR THE BOOSTER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 53,0
- Geschlecht
- M
- Eingang
- 24.02.2022
- Impfdatum
- 24.02.2022
- Beginn
- 24.02.2022
- 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
Medication error
Symptomtext
MEDICATION ERROR - GAVE 0.5 INSTEAD OF 0.25
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- UNK
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- 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 temperature excursion issue
Symptomtext
Doses administered after temperature excursion; Doses administered after temperature excursion; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses administered after temperature excursion) and PRODUCT TEMPERATURE EXCURSION ISSUE (Doses administered after temperature excursion) in a 42-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 07-Feb-2022 at 8:30 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 07-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses administered after temperature excursion) and PRODUCT TEMPERATURE EXCURSION ISSUE (Doses administered after temperature excursion). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses administered after temperature excursion) and PRODUCT TEMPERATURE EXCURSION ISSUE (Doses administered after temperature excursion) outcome was unknown. The action taken with mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. Vaccine was administered on left side intramuscularly. No concomitant products were reported. No adverse event reported. No treatment details were reported. On Monday 07-Feb-2022 at 8:00 am, the digital readout on data logger reading -22.5 degree F for freezer and 19.9 degree F for refrigerator. Vaccine bottles from refrigerator had no signs of freeze, which meant no ice or crystallized solids in the vaccine bottle. The refrigerator temperature controller dial adjusted to 5 from initial number 7. No water bottles in refrigerator and frozen coolant packs in freezer at that time or any other times. At 9:11 am, refrigerator data logger reading was 27.7 degree F. Freezer data logger reading was -10.3 degree F. The temperature controller dial was on number 5. At 9:55 am on 07-FEB-2022, refrigerator data logger reading was 32.5 degree F and freezer data logger reading was -0.9 degree F.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 22.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product temperature excursion issue
Symptomtext
Doses administered to 3 patients after temperature excursion; Temperature excursion; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Doses administered to 3 patients after temperature excursion) and PRODUCT TEMPERATURE EXCURSION ISSUE (Temperature excursion) in a 62-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 07-Feb-2022 at 8:40 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 07-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Doses administered to 3 patients after temperature excursion) and PRODUCT TEMPERATURE EXCURSION ISSUE (Temperature excursion). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Doses administered to 3 patients after temperature excursion) and PRODUCT TEMPERATURE EXCURSION ISSUE (Temperature excursion) outcome was unknown. Not Provided For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant medications were reported. No Treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- LA
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 20.01.2022
- Beginn
- 17.02.2022
- Tage bis Beginn
- 28,0
- Dosis
- 1
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Dose administered to 2 patients after more than 30 days stored in the refrigerator; Product storage error; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose administered to 2 patients after more than 30 days stored in the refrigerator) and PRODUCT STORAGE ERROR (Product storage error) in a 23-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 060H21A and 001J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 20-Jan-2022, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 17-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose administered to 2 patients after more than 30 days stored in the refrigerator) and PRODUCT STORAGE ERROR (Product storage error). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose administered to 2 patients after more than 30 days stored in the refrigerator) and PRODUCT STORAGE ERROR (Product storage error) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was provided No treatment medication was provided. This case was linked to MOD-2022-489166 (Patient Link). Most recent FOLLOW-UP information incorporated above includes: On 18-Feb-2022: Significant FU appended- dose 1 and dose 2 details and patient details were added
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received her 2nd dose of Moderna from a refrigerated vial expired by 11 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 25,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 14.02.2022
- Beginn
- 14.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received her 2nd dose of Moderna from a refrigerated vial which had expired by 11 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 09.02.2022
- Beginn
- 09.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Patient received booster dose of Moderna vaccine from an expired vial which had been kept in refrigerator. Vial expired on 2/3/22 and dose given on 2/9/22.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 30,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 16.02.2022
- Beginn
- 16.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
No adverse event
Symptomtext
No adverse event known. Pt given 2nd dose of Moderna from a vaccine bottle which had been refrigerated, but expiration date had passed by 13 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- none.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product temperature excursion issue
Symptomtext
The HCP stated that 3 doses were administered from the opened vial/ Temperature excursion; Temperature excursion; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (The HCP stated that 3 doses were administered from the opened vial/ Temperature excursion) and PRODUCT TEMPERATURE EXCURSION ISSUE (Temperature excursion) in a 61-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 07-Feb-2022 at 8:40 AM, the patient received first dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On 07-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (The HCP stated that 3 doses were administered from the opened vial/ Temperature excursion) and PRODUCT TEMPERATURE EXCURSION ISSUE (Temperature excursion). At the time of the report, EXPIRED PRODUCT ADMINISTERED (The HCP stated that 3 doses were administered from the opened vial/ Temperature excursion) and PRODUCT TEMPERATURE EXCURSION ISSUE (Temperature excursion) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. Reporter reported that 3 doses were administered among which 2 doses were booster and 1 dose was a full dose. Excursion temperature maximum 33.4 degrees Fahrenheit and minimum 19.5 degrees Fahrenheit. Excursion occurred on 07-Feb-2022 with the duration of 612 minutes. Vails were stored at room temperature and were moved from freezer to refrigerator on 04-Feb-2022. Vails looked normal on visual inspection. patient doesn't experienced any side effect 8:00 am Monday (07-FEB-2021) Digital readout on data logger reading -22.5F for freezer and 19.9F for refrigerator. vaccine bottles from refrigerator had no signs of freeze, i.e. no ice or crystallized solids in the vaccine bottle the refrigerator temperature controller dial adjusted to 5 from initial number 7. no water bottles in refrigerator and frozen coolant packs in freezer at this time or any other times. 9:11 am (07-FEB-2021) refrigerator data logger reading is 27.7F freezer data logger reading is -10.3F. the temperature controller dial is on number 5 9:55 am (07-FEB-2021) refrigerator data logger reading is 32.5F and freezer data logger reading is -0.9F. No treatment medications were provided. Most recent FOLLOW-UP information incorporated above includes: On 17-Feb-2022: Patient demographics updated, product details updated, new Event added.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 18.02.2022
- Impfdatum
- 15.02.2022
- Beginn
- 15.02.2022
- 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
Patient should have been given a booster dose and instead he received a full third dose of Moderna because he marked that it was his second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- -
- Geschlecht
- U
- Eingang
- 16.02.2022
- Impfdatum
- 08.02.2022
- Beginn
- 08.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Dose given past expiration date; This spontaneous case was reported by a pharmacist and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Dose given past expiration date) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 001J21-2A) for COVID-19 vaccination. No Medical History information was reported. On 08-Feb-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 08-Feb-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Dose given past expiration date). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Dose given past expiration date) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medications were reported. Refrigerator expiration date reported as 05-Feb-2022 as it was removed from freezer on 06-Jan-2022. No temperature excursion was reported during storage. No treatment medications were reported. Most recent FOLLOW-UP information incorporated above includes: On 11-Feb-2022: Non significant follow up received.
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
- 16.02.2022
- Impfdatum
- 03.01.2022
- Beginn
- 03.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Symptomtext
A 17-year-old patient inadvertently given Moderna (dose #1), which is indicated for ages 18+.
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
- 17,0
- Geschlecht
- M
- Eingang
- 15.02.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OR
- Alter
- 15,0
- Geschlecht
- U
- Eingang
- 14.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 04.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- 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 received Moderna booster, Patient is not 18 and not eligible to receive Moderna and should have received 12+ Pfizer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 14.02.2022
- Impfdatum
- 07.02.2022
- Beginn
- 07.02.2022
- 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 administered to patient of inappropriate age
Symptomtext
Moderna given to patient under the age of 18. NO Adverse adverse event was experienced from patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknow
- Vorgeschichte
- unknow
- Andere Medikamente
- unknown
- Allergien
- unknow
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 11.02.2022
- Impfdatum
- 11.02.2022
- Beginn
- 11.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Fall
Symptomtext
The patient got weak and went to the floor.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- n/a
- Aktuelle Erkrankungen
- not known
- Vorgeschichte
- n/a
- Andere Medikamente
- not known
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 11.02.2022
- Impfdatum
- 10.02.2022
- Beginn
- 10.02.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient requested and received a moderna vaccine and was later found to be under 18 by pharmacist
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 10.02.2022
- Impfdatum
- 16.01.2022
- Beginn
- 16.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Dysphagia
Symptomtext
Patient was in the observation area when the incident occurred. He refers to feeling discomfort when swallowing after the administration of the vaccine. Doctor was consulted and ordered to administer 50mg of BENADRYL P.O.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Discomfort
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Synthroid; Clonazepam
- Allergien
- Contrast
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Interchange of vaccine products
Unevaluable event
Symptomtext
It was discovered that this patient had received Jansen COVID vaccination on 9/9/21. Instead of receiving .25ml of Moderna for the booster dose, patient received a full dose of .5ml of Moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Interchange of vaccine products
Unevaluable event
Symptomtext
It was discovered that this patient had received Jansen COVID vaccination on 9/9/21. Instead of receiving .25ml of Moderna for the booster dose, patient received a full dose of .5ml of Moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 81,0
- Geschlecht
- F
- Eingang
- 07.02.2022
- Impfdatum
- 23.01.2022
- Beginn
- 25.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blister
Erythema
Peripheral swelling
Symptomtext
Patient stated her fingers in the administration arm became red, sore, and had some blisters from the fingernail to the first joint. She explained that they are improving without treatment, but she wanted us to report. She said she cannot take any sort of steroids due to steroid sensitivity and was overall ok with the improvement on its own.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blister
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None that patient was aware of
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Losartan
- Allergien
- -
- Vorherige Impfungen
- Near Death to Pox Vaccine
- Staat
- WI
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 07.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 07.02.2022
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
PATIENT PRESENTED FOR FIRST MODERNA .5ML WHICH IS A HIGHER DOSE THAN AUTHORIZED. DOCTOR WAS NOTIFIED.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KS
- Alter
- 50,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 04.02.2022
- Beginn
- 05.02.2022
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
No adverse event
Symptomtext
PT CAME IN FOR A BOOSTER DOSE OF THE COVID-19 VACCINE. HIS FIRST DOSE WAS OF JANSSEN. A BOOSTER DOSE OF MODERNA WAS REQUESTED BY THE PATIENT. HE WAS GIVEN A FULL DOSE OF 0.5ML MODERNA INSTEAD OF THE BOOSTER DOSE OF 0.25ML OF MODERNA. PT WAS OBSERVED FOR 15 MINUTES AFTER RECEIVING THE VACCINE AND DID NOT HAVE ANY S/S OF ADVERSE REACTIONS. THE ERROR WAS NOT DISCOVERED UNTIL AFTER THE PT HAD LEFT THE CLINIC. THE PT. WAS NOT NOTIFIED OF THE ERROR.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN. NONE LISTED
- Vorgeschichte
- -
- Andere Medikamente
- UNKNOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 16,0
- Geschlecht
- F
- 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: nein
Wrong product administered
Symptomtext
GIVEN MODERNA INSTEAD OF PFIZER
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Wrong product administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NO
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 05.02.2022
- Impfdatum
- 03.01.2022
- Beginn
- 05.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Erectile dysfunction
Symptomtext
Erectile disfunction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Erectile dysfunction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Excellent
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 04.02.2022
- Impfdatum
- 17.01.2022
- Beginn
- 17.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Lip swelling
Symptomtext
Patient states that at 4:30pm on 01/17/22 the lip of her mouth begun to swell and at 7:49 pm she arrived at the emergency room of Doctors where she was administered Solumedrol- and BENADRYL, patient was discharged.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lip swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Patient reports that before being vaccinated she took Tylenol.
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 22,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 63,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
Patient did not have any reaction.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
patient did not have any reaction
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 03.02.2022
- Impfdatum
- 19.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Symptomtext
no reaction present
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 69,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 01.02.2022
- Beginn
- 01.02.2022
- 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 a full 0.5 ml dose of the 4th booster dose for an immunocompromised patient
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Ovarian Cancer, A-Fib, Hypokalemia, Osteoporosis
- Vorgeschichte
- Ovarian Cancer
- Andere Medikamente
- Potassium Chloride, Metoprolol, Oxybutynin Chloride, Norco, Phenazopyridine, Compazine, Loperamide, Iron, Lorazepam, Magnesium Citrate, Mekinist, Colace, Famotidine, Faslodex
- Allergien
- Penicillin, Pine, Fosamax, CT Dye
- Vorherige Impfungen
- -
- Staat
- WI
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 01.02.2022
- Impfdatum
- 13.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Cyanosis
Symptomtext
Both hands turned blue from 7:30pm to 1:30 am 6 hours. No other symptoms at all. Came second dat after booster vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cyanosis
- Hospital-Tage
- -
- Labordaten
- Did not need to go in.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Asthma
- Andere Medikamente
- Losartan 100mg once daily/ omerprozole once a day/ Amlotdipine 5mg once a day/ Asmanex 1-2 puffs @ hs/ coQ10 / vitamin D 3 / magnesium/ Zyrtec
- Allergien
- Flu vaccine / amoxicillin / statins
- Vorherige Impfungen
- Flu vaccine in 1967 hives throat started to swell shut in hospital.
- Staat
- TX
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 30.01.2022
- Impfdatum
- 28.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Burning sensation
Nasal discomfort
Symptomtext
Prolonged sinus burning and burning in neck and lower back 24 hours after first covid vaccine Moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Burning sensation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Acetaminophen 500 mg Benadryl 25 mg
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 29.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Wrong product administered
Symptomtext
No adverse event at this moment. Patient received the wrong vaccine. Patient received ? dose (0.25mL) of Moderna. The only vaccine patient qualified to receive is Pfizer (12 and above).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- N/A
- Allergien
- No known allergy
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 29.01.2022
- Impfdatum
- 29.01.2022
- Beginn
- 29.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
dose 2 in primary series administered too early at 21 days (instead of 28 days)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 73,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 26.01.2022
- Beginn
- 28.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
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
RESIDENT RECEIVED PFIZER VACCINE ON 1/21/22 WHEN RESIDENT DISCHARGED FROM HOSPITAL. WHEN RESIDENT ADMITTED TO FACILITY DAUGHTER SIGNED CONSENT FORM FOR VACCINE AND REPORTED THAT RESIDENT DID NOT RECEIVE VACCINE. ON 1/26/22 RESIDENT WAS GIVEN MODERNA VACCINE. RESIDENT DOES NOT HAVE ANY ADVERSE REACTIONS AT THIS TIME.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 06.01.2022
- Beginn
- 19.01.2022
- Tage bis Beginn
- 13,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Herpes zoster
Ophthalmic herpes zoster
Symptomtext
Shingles left side of face including eye and scalp
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin d3 Vitamin c
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- AK
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 23.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- 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
Inappropriate schedule of product administration
No adverse event
Symptomtext
Patient did not have any adverse events. We discovered after I administered the Moderna vaccine that she had already had the Moderna booster 0.25 mL on 10/22/21. Lot# 091D21A, Exp. 12/12/21. She said she was due for #3.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- anemia, ETOH abuse, eczema
- Andere Medikamente
- None
- Allergien
- amoxicillin, crab
- Vorherige Impfungen
- -
- Staat
- MD
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 22.01.2022
- Impfdatum
- 22.01.2022
- Beginn
- 22.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Patient came in for an appointment for Moderna booster. He presented his vaccine card which indicated he had received the first dose June 2021 and second July 2021, so he was due for his booster dose. Confirmed w/ the patient he wanted the Moderna booster and administered the shot. After giving the dose the patient asked if mixing and matching manufacturers was ok and I responded that it was according to the CDC. He said that he had gotten the J & J vaccine and booster, but he wanted Moderna because he heard it was more effective. I questioned that because according to the vaccine card he presented he had gotten Moderna initially, and again today. He then stated, oh I have another vaccine card, which he removed from his wallet, and it had his name and DOB and indicated that he had gotten an initial J & J dose in April 2021 and a second November 2021. I confirmed this information on system. The patient departed the pharmacy not complaining of any adverse effects, but I had never encountered someone getting that many doses and wanted to report it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 21.01.2022
- Impfdatum
- 21.01.2022
- Beginn
- 21.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Moderna vaccine was given to a patient under the age of 18 years old. No current side effects or symptoms have been reported by mother
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 20.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
Child is 15, accidentally gave Moderna half dose for booster vaccine verses Pfizer booster dose. Child tolerated well, have informed Parent of dosing of Moderns vs Pfizer.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 10.01.2022
- Tage bis Beginn
- 3,0
- 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
Patient or patient's representative registered online to receive their first dose of Moderna Covid19 vaccine. The patient was 16 years old, rather than the minimum age of 18 required to receive the Moderna brand vaccine. Pharmacist administering vaccine did not realize patient was under the required age and administered the dose. Patient did not experience side effects from the vaccine. Local Department of Public Health contacted the pharmacy 3 days later to point out the error after reviewing the local Immunization Registry. Pharmacy contacted patient's father to explain error and prepare them to select the Pfizer vaccine when registering for their second dose. Patient's father was understanding. Pharmacy subsequently updated their online form to show eligible patient age range in parentheses for each brand of Covid19 vaccine offered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 14,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 20.01.2022
- Beginn
- 20.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product administered to patient of inappropriate age
Wrong product administered
Symptomtext
The patient and the mother of the minor are advised of the vaccine to be administered (Pfizer) as appropriate and as already written on the vaccination card for both. At the time of administering the vaccine (PFIZER) Patient asked me if she and her son wanted it to be Moderna; which I administered according to request by mother. The mother is advice regarding the age indicated for this vaccine, the mother is advised to report any secondary effect of the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 16,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient received Moderna. Not yet approved for the age group as the primary dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- n/a
- Vorgeschichte
- n/a
- Andere Medikamente
- n/a
- Allergien
- n/a
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 13,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 15.01.2022
- Beginn
- 15.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
Patient received Moderna. Age group not currently approved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 23,0
- Geschlecht
- M
- Eingang
- 20.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
Given 0.25ml instead of 0.5ml for second dose. Pt was contacted on 01/15/2022 and offered another dose of 0.25ml. He declined. He was told that due to the lesser dose he did not complete the series to be considered fully vaccinated. He still did not want.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient received booster 5 days before he should have. 1 day before the allowable 4 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 18.01.2022
- Beginn
- 18.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Patient and father checked in for Pfizer booster vaccine. Before administration, patient's father requested with nurse that the Moderna booster vaccine be administered instead. Administering nurse administered Moderna booster vaccine without confirming with pharmacy staff.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKOWN
- Allergien
- NONE
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient was given a booster dose of Moderna less than 6 months from her second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NV
- Alter
- 45,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Patient given a booster dose of Moderna less than 6 months from his second dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
The patient was given Moderna, but she was not yet 18 years of age. The patient did not have any signs or symptoms at the time of reporting.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 17.01.2022
- Impfdatum
- 13.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Nodule
Oedema peripheral
Symptomtext
Swollen armpit on left side. Knot on left shoulder blade
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nodule
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 15,0
- Geschlecht
- F
- Eingang
- 17.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
No adverse event
Product administered to patient of inappropriate age
Product administration error
Symptomtext
No adverse event, administration error. Patient requested Moderna booster after her Pfizer series but is not old enough to get Moderna. Administering pharmacist did not catch she was too young until after the shot was administered.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AL
- Alter
- 18,0
- Geschlecht
- M
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Patient came to get his first dose of Covid 19 moderna vaccine. He received 0.25 ml initially and the error was realized immediately and explained to the patient. He was then given 0.25ml on the same arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- UNKNOWN
- Vorgeschichte
- UNKNOWN
- Andere Medikamente
- UNKNOWN
- Allergien
- UNKNOWN
- Vorherige Impfungen
- -
- Staat
- AR
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test positive
Symptomtext
hospitalization with covid after being fully vaccinated with a booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- positive covid pcr 1/12/22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- (last Echo 09/27/21: EF 35 to 40%), COPD (2L of oxygen at home), CAD s/p multiple stent placements, CKDIII, Afib on Apixaban, HTN, HLD
- Andere Medikamente
- unknown
- Allergien
- adhesive tape
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 14.01.2022
- Impfdatum
- 14.01.2022
- Beginn
- 14.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Product administered to patient of inappropriate age
Symptomtext
A 13 year old patient was administered a dose of Moderna .25cc. There was no adverse reaction and no negative symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Autism
- Andere Medikamente
- N/A
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Underdose
Symptomtext
GIVEN HALF-DOSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
GIVEN HALF-DOSE.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 12.01.2022
- Impfdatum
- 12.01.2022
- Beginn
- 12.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Product administered to patient of inappropriate age
Symptomtext
Vaccine was administered to a 17 year old female. Moderna has EUA for 18 years and older.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- Unknow
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- PR
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
During the interview, the nurse ask to the patient which previous dose she had administered and she indicates that she has been administered the COVID 19 Moderna vaccine. After a consult with the medical director of the facility, from which dose correspond to the patient due to her medical history either a 0.25 ml or a 0.50 ml dose, Dr. indicates that the corresponding dose is 0.50 ml. After administration of the vaccine, when the form was in the quality area, the employee notice that the previous dose was 0.50 ml of COVID19 Janssen vaccine. After this event, a consult was made with Dr. due to that there was an erroneous administration of the vaccine due that the corresponding dose should have been 0.25 ml since it is considered a booster, as it has been established in the CDC guidelines.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chron's Syndrome
- Andere Medikamente
- Humira 80 mg - Imuran 50 mg -
- Allergien
- Renflexis - which induces anaphylactic shock
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 11.01.2022
- Impfdatum
- 11.01.2022
- Beginn
- 11.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Patient was due for COVID booster. Administered Moderna Booster to patient who is 17 years and 4 months old. Consulted with supervising physician and chief nursing officer for clinical practice group. Patient and parent of patient are aware. No adverse events occurred post vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 07.01.2022
- Beginn
- 09.01.2022
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Lymphadenopathy
Symptomtext
Swollen lymph node under left arm and left side of neck, both are very large 3 - 5 inches in size
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 12,0
- Geschlecht
- F
- Eingang
- 06.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
pt is only 12 years old and received the moderna vaccine - which is not recommended for this pt age. Moderna was contacted - case # MOD22-001168. was told to just monitor pt but should be safe and no further action required by pharmacy,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none -
- Allergien
- none
- Vorherige Impfungen
- -