- Staat
- -
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 27.03.2023
- Impfdatum
- 05.11.2021
- Beginn
- 13.02.2023
- Tage bis Beginn
- 465,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Acute respiratory failure
Angiogram pulmonary abnormal
Asthenia
Brain natriuretic peptide increased
COVID-19
COVID-19 pneumonia
Cough
Dyspnoea
Echocardiogram normal
Endotracheal intubation
Gastrointestinal haemorrhage
Lung opacity
Mental status changes
Physical deconditioning
SARS-CoV-2 test positive
Seizure
Shock haemorrhagic
Symptomtext
Patient is a 70 y.o. female with a history of Afib,HTN, L MCA stroke s/p NIR for TICI 2c reperfusion, Asthma and morbid obesity who was admitted 2/6/23 for AMS , Seizure and found to have hemorrhagic shock due to GIB and acute respiratory failure requiring intubation. She was just discharged home with HHC after she refused facility and represented RMH 2/13/2023 with cough and increased SOB. She was found to have positive COVID-19. CTPA without PE, noted b/l GGO. Discharged to home w/ HHC 2/17/23. 1. COVID-19 Pneumonia: Vaccinated. Test positive 2/13/23. CTPA as above. Of not pt was intubated from 2/6-2/9/23 and weaned to room air prior to discharge. Hypoxia noted and initiated decadron and remdesivir 2/15/23. Improved. 2. Acute Hypoxic Respiratory Failure: due to COVID-19. BNP 7000s. TTE 02/2023 with EF 50-55%. On room air and not overloaded on exam. Given IV Lasix x1. Did not qualify for home O2. Resolved. 3. Generalized weakness: due to recent critical admission and deconditioning. Reportedly pt refused SNF on prior admission and dc with HHC. Therapies followed
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute respiratory failure
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 09.02.2023
- Impfdatum
- 23.06.2022
- Beginn
- 08.10.2022
- Tage bis Beginn
- 107,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Infection
Symptomtext
Patient had a breakthrough infection and passes away.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- SD
- Alter
- 75,0
- Geschlecht
- M
- Eingang
- 06.01.2023
- Impfdatum
- 04.11.2021
- Beginn
- 05.10.2022
- Tage bis Beginn
- 335,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Acute kidney injury
COVID-19
Death
Dehydration
Fall
Lumbar vertebral fracture
Respiratory symptom
SARS-CoV-2 test positive
Spinal compression fracture
Vaccine breakthrough infection
Symptomtext
This is an instance of breakthrough COVID-19 after which death occurred. The individual was vaccinated with the Moderna product on 02/17/2021, 03/17/2021, and 11/04/2021. They had recently been hospitalized 09/14/2022-09/30/2022 after suffering complications of a L1 compression fracture after a fall. They were discharged to a skilled nursing facility after this hospitalization. They tested positive for COVID-19 on 10/05/2022, when they were admitted to the hospital for dehydration and management of respiratory symptoms. The individual had many underlying medical conditions. They were found to have an acute kidney injury. They were discharged back to skilled nursing facility on 10/08/2022. They died on 10/15/2022. I see no indication they were hospitalized closer to the death date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Chronic Respiratory Failure, Congestive Heart Failure, A-Fib, Chronic Kidney Disease, Diabetes Mellitus, Hypertension, COPD, Alzheimer's Dementia (with frequent falls, failure to thrive, confusion, and hallucinations), Hyperlipidemia. Osteoarthritis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 23.05.2022
- Impfdatum
- 08.11.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 31,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Anticoagulant therapy
COVID-19
COVID-19 pneumonia
Chest X-ray abnormal
Death
Dysphagia
Dyspnoea
Hypoxia
Lung infiltration
Nothing by mouth order
Positive airway pressure therapy
SARS-CoV-2 test positive
Ventricular tachycardia
White blood cell count normal
Symptomtext
12/9/2021 - Sent to ER from Oncology for SOB/hypoxia and immunocompromised due to 3/5 chemo completed for stage IV lung Ca. POC Covid test positive. On arrival temp 37, RR 18, SpO2 94 on supp O2, BP 131/87, WBC 7.7. Chest xray revealed bilateral infiltrates concerning for Covid 19. Admitted to Telemetry for covid pneumonia. Started on Vancomycin, Cefepime, Decadron, Lovenox, and Remdesivir. 12/10 - Baricitinib added to treatment. On high flow NC for O2, FiO2 65% with 40L flow. BP 152/95, HR 123. 12/11 - having asymptomatic runs of V tach and dissiculty swallowing. Kept NPO. O2 requirements not improving but not worsening. Changed steriod to Solu-medrol on 12/12. mech diet initiated 12/14- 5 day course Remdesivir complete. Baricitinib d/c 12/13 - WBC trending down. increasing hypoxia/HR - Hypoxia/tachycardia increasing -placed on BiPAP 100% FiO 12/15 - Decision for Palliative /comfort care vs aggressive treatment. 12/18 - Patient expired @1220.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, BPH, Hypothyroid, Hyperlipidemia, diabetes, OSA on CPAP, Lung Ca-IV, Bone Mets, fatigue
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 85,0
- Geschlecht
- M
- Eingang
- 02.05.2022
- Impfdatum
- 08.11.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 54,0
- Dosis
- 3
- Route/Site
- - / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Death
Dyspnoea
General physical health deterioration
Hypoxia
Oxygen saturation decreased
Pneumonia
Respiratory disorder
SARS-CoV-2 test positive
Symptomtext
pt presents to ED with worsening SOB; pt states he's had trouble with pneumonia over the past month and has been on multiple ABX; was seen at an urgent care a few days ago, was tested for COVID but unsure of the results; pt found to be positive for COVID in ED; hypoxic with O2 sats in low 80s%; O2 supplementation; baricitinib and dexamethasone; pt's respiratory status worsened; status changed to DNR/DNI; pt desaturates with minimal exertion; pt continued to worsen and he passed away in the hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- 9,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- LYMPHOMA
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 14.12.2021
- Beginn
- 25.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Activated partial thromboplastin time
Acute myocardial infarction
Alanine aminotransferase normal
Antimicrobial susceptibility test sensitive
Aspartate aminotransferase normal
Back pain
Bacteraemia
Bacterial infection
Bacterial test positive
Bandaemia
Bilirubin urine
Blood alkaline phosphatase normal
Blood bilirubin increased
Blood chloride decreased
Blood creatinine increased
Blood culture positive
Blood gases
Blood glucose increased
Symptomtext
76/F pt with obesity (current BMI 33), DM, diabetic CKD (baseline creatinine 1.01-1.07), HTN, HLD, asthma, fully vaccinated for COVID including booster, was in USOH until diagnosed with COVID on 12/21. She was having dysuria for 2 days prior, had a TAV as she started having fever and vomiting x 1. On AM of admit she woke up with shaking chills, and dyspnea -> called EMS and came to ED where she was noted to be hypoxic to 90% and hence was placed on 2 L of O2. She was given LR due to UTI + COVID. ROS on admit positive for back pain, and nausea. She lives with her family at home, independent for ADL's, daughter and grand daughter both had tested + for covid (12/20 and 12/17 respectively), her husband is negative. Vitals on arrival T-101.4, 84, 23, 96-99 % on 2 L, BP 115/56. Labs notable for cr of 1.28 (bl 1.0-1.07, GFR in CKD 3a range), elevated lactate at 2.0 (improved to 1.5 with LR total of 500 cc), CRP of 10.3, Covid positive, WBC normal on admit but with bandemia, d-dimer 1.71, UA was positive and CXR negative for focal infiltrates or congestion. She met criteria for severe sepsis on admit. UTI with pyelonephritis Keflex given in ED, changed to Ceftriaxone on admit. 2/2 blood cx's growing E Coli. Urine cx also with E.Coli (sensitive to cefazolin, no prior positive urine cx's in the system) - Continue Ctx per d/w ID through today, will change to Cipro at discharge to complete 14 day course. Covid positive status. Brief hypoxia to 90% on RA on arrival. Brief dry cough per history. Was started on dexamethasone (received total of 2 doses 12/25 and 12/26). Had brief hypoxia of 90% in ED (while febrile), since then recovered. Currently on RA saturating 98%. Also has negative CXR. - Stopped steroids per d/w ID, given she has active bacteremia and underlying DM. - Not given Remdesivir d/t elevated creatinine. Also hypoxia was brief. Enhanced isolation to continue for total of 10 days through 1/1/22, considered mild infection. D/W Dr./ID. - CRP up from 10.3->13.8 but could be from bacterial infection. - LFT's are normal. D-dimer 1.71->1.55. Elevated troponin No EKG changes. Likely type 2 MI in the setting of severe sepsis. PTA ASA/statin continued. Telemetry monitoring for now Troponin peaked at 0.40 (0.08-> 0.40-> 0.21). Pt had no exertional symptoms prior to getting sick, hence no out pt ischemia w/u recommended per Dr./Cardiology. Mild persistent asthma On Wixela and prn Albuterol. DM2 with CKD stage 3A. Glipizide and Metformin on hold NPH (7 units BID new) with SSI started on admit. Current FS values in 200-300's, from steroid use in the setting of DM. Last A1C was 7.2 in 10/2021 (prior was 10.3 in 01/2021). - Increased NPH to 10 U BID AC for elevated blood sugars while here. - Resume home regimen on discharge. HTN/HLD On PTA Amlodipine and statin. ACEi held on admission d/t rise in creatinine. Reason for Hospital Admission (Admitting Diagnosis): SOB and UTI
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Acute myocardial infarction
- Hospital-Tage
- 3,0
- Labordaten
- Recent Labs 12/25/21 1029 NA 132* K 3.7 CO2 25 CL 96* BUN 24 CR 1.28* RBS 112 CBC Recent Labs 12/25/21 1029 WBC 4.1 HGB 12.0 HCT 36.1 PLT DECREASE* | 141 | NORMAL MCV 96 NEUT 69 Cardiac Recent Labs 12/25/21 1050 TROP 0.08* LFTs Recent Labs 12/25/21 1029 AST 32 ALT 20 ALKP 88 TBILI 1.3* LIPASE 17 Coags No results for input(s): PT, INR, PTT in the last 72 hours. ABG No results for input(s): PH, PO2, PCO2 in the last 72 hours. Anti-XA No results for input(s): HEPUNFR, FACTXAINHIB in the last 72 hours. Lab Results Component Value Date Lactate, ser/plas 1.5 12/25/2021 Lactate, ser/plas 2.0 (AA) 12/25/2021 Lab Results Component Value Date Cholesterol 150 10/18/2021 Triglyceride 119 01/19/2021 HDL 67 10/18/2021 Low density lipoprotein calculated 60 01/19/2021 LDL CALCULATED, NONFASTING 70 10/18/2021 TRIGLYCERIDE, NONFASTING 67 10/18/2021 Lab Results Component Value Date Hgb A1c % 7.2 (H) 10/18/2021 Lab Results Component Value Date TSH 4.7 10/18/2021 Recent Labs 12/25/21 1050 UPH 5.0 USG 1.012 UAGLU NEGATIVE UKET NEGATIVE UABILI NEGATIVE UPROTEIN >500* ULEUKESTER MODERATE* UNITRITE POSITIVE* URBC 8* UWBC 180* UBACT 1+*
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- obesity (current BMI 33), DM, diabetic CKD (baseline creatinine 1.01-1.07), HTN, HLD, asthma
- Andere Medikamente
- Outpatient Medications: confirmed with Patient Prior to Admission Medications Outpatient Home Medications Taking? Albuterol (PROAIR/PROVENTIL/VENTOLIN) 90 mcg/actuation Inhl HFAA Takes Occasionally Sig: Inhale 2 Puffs by mouth every 4 hours
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- MO
- Alter
- 57,0
- Geschlecht
- M
- Eingang
- 22.12.2021
- Impfdatum
- 12.02.2021
- Beginn
- 27.11.2021
- Tage bis Beginn
- 288,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Death
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Multiple schlerosis
- Andere Medikamente
- Unknown
- Allergien
- Unknown
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 16.11.2021
- Impfdatum
- 13.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Anticoagulant therapy
Chest pain
Computerised tomogram thorax abnormal
Deep vein thrombosis
Dyspnoea
Pulmonary embolism
Symptomtext
Presented with chest pain and acute shortness of breath, found to have bilateral sub-segmental PE with LLE DVT, treated with UF Heparin. Hospitalization ongoing (day 3).
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary embolism
- Hospital-Tage
- -
- Labordaten
- 11/14: CTPE positive for bilateral sub-segmental PE
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HFpEF T2DM Hyperlipidemia Acquired hypothyroidism Morbid obesity MDD Essential hypertension Chronic L foot ulcer/ osteomyelitis Chronic coronary artery disease Peripheral neuropathy Psoriasis CKD stage 3b Seborrheic dermatitis OSA Aortic Stenosis s/p pbAVR COVID-19 Pneumonia
- Andere Medikamente
- Acetaminophen Ascorbic acid with rose hips aspirin atorvastatin buspirone calcium citrate clonazepam docusate famotidine ferrous sulfate insulin glargine ketoconazole 2% cream levothyroxine melatonin metformin metoprolol succinate multivita
- Allergien
- surgical tape
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 101,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Aspiration
Death
General physical health deterioration
Symptomtext
On 11/12/21 @ approximately 1:11 pm resident 02 saturation decreased to 84%. rebounded after breathing treatment to 91% but residents overall condition continued to decline. 02 increased to 3 liters with orders to titrate up to 6 liters. This resident was a hospice patient and had been having recent episodes of aspiration. Condition continued to decline and resident expired on 11/15/21 @ approximately 9:44 am
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Death
- Hospital-Tage
- -
- Labordaten
- None due to hospice status
- Aktuelle Erkrankungen
- HEART FAILURE, HOSPICE/PALLATIVE CARE, PROTEIN CALORIE MALNUTRION, PAIN, ANXIETY DISORDER, DRY EYE SYNDROME, SHORTNESS OF BREATH, DEMEMTIA WITHOUT BEHAVIORAL DISTURBANCE, ESSENTIAL HYPERTENSION, HYPOTHYROIDISM, GLAUCOMA, MACULAR DEGENERATION, CONSTIPATION, MAJOR DEPRESSIVE DISORDER, DEPENCE ON SUPPLEMENTAL 02, HEARING LOSS, BILATERAL
- Vorgeschichte
- HEART FAILURE, MACULAR DEGENERATION , 02 DEPENDANCE WITH SOB, HTN, GLAUCOMA AND MACULAR DEGENERATION
- Andere Medikamente
- Lorazepam 0.5mg q4hrs prn restlessness/anxiety, Morphine sulfate concentrate solution 20 mg/ml- give 0.25 ml q 30 minutes PRN breakthrough pain/air hunger and 0.5 ml q 4hr prn pain, air hunger.
- Allergien
- PCN and calamine
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 02.06.2022
- Impfdatum
- 06.11.2021
- Beginn
- 01.04.2022
- Tage bis Beginn
- 146,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Bell's palsy
Tinnitus
Symptomtext
Patient reports having developed Bell's Palsy and ringing in the ears about 5 months after receiving the vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Diabetes, Hypertension
- Andere Medikamente
- Metformin, Amlodipine
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 21.05.2022
- Impfdatum
- 02.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: ja
Disable: ja
ER: ja
Erholt: nein
Angina pectoris
Bell's palsy
Cardiomyopathy
Chest pain
Computerised tomogram
Feeling abnormal
Headache
Injection site pain
Laboratory test
Magnetic resonance imaging
Neoplasm malignant
Pain
Psychotic disorder
Pyrexia
Rash
Symptomtext
11/02/2021 date I had the Moderna booster vaccine. 11/03/2021 date I started feeling kind of weird then a couple days later , after continuing to feel bad each day after I was hospitalized due to myocardial, bell's palsy, psychosis, severe headaches, body aches, pain in my heart/chest, rash on my neck, fever, my arm I had the shot in has felt like it's constantly burning,fire,like rope burns since then. Since Nov 2nd 2021 that I received the Moderna booster Vaccine my health has went from completely healthy to being hospitalized again with Cancer. All due to this booster vaccine I took.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- MRIs ,CT scans, labs, I have have so much done, been to family dr after dr begging for referrals, been hospitalized twice. There is so much Medically since I got the Moderna booster vaccine it's unbelievable. I was completely healthy before taking that booster. 11/2021 til April 25th,2022 when I was hospitalized a second time and found out I have Cancer
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- Muscle relaxers
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 27.04.2022
- Impfdatum
- 24.11.2021
- Beginn
- 22.04.2022
- Tage bis Beginn
- 149,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
COVID-19
Cough
Fatigue
Heart rate increased
Influenza like illness
Pain
Pain in extremity
Pyrexia
Respiratory disorder
SARS-CoV-2 test positive
Thrombosis
Weight bearing difficulty
White blood cell count increased
Symptomtext
He started with a cough, and it progressed to being very fatigue and the cough got stronger. On Saturday, he went to Urgent Care and he tested positive for COVID-19. He was experiencing flu like symptoms. He then started to experience body aches especially in his legs. He started to have a fever of 100.4. By 04/25/2022, he was so fatigued he was having trouble carrying his weight. He also started experiencing respiratory issues and an increase heartrate of 119. He went to the emergency room. The doctor said his white blood cell count was high. They admitted into the hospital and are treating for the elevated white blood cells and blood clots. His fever has resolved, and his cough sounds better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- Common Cold
- Vorgeschichte
- Sleep Apnea, High Cholesterol
- Andere Medikamente
- Multivitamin, Lipitor 80mg once daily, Prilosec 20mg once daily.
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 24.01.2022
- Impfdatum
- 05.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Bell's palsy
Eye pain
Facial paralysis
Swelling face
Symptomtext
Bell's Palsy Left eyelid has been drooping closed x 2 wk. Pain in eye is inside eye, feels like something pulling from inside. Face on left also swollen.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Bell's palsy
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 27,0
- Geschlecht
- M
- Eingang
- 15.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 08.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Hyperhidrosis
Pallor
Presyncope
Symptomtext
5mins post vaccination pt reported that he was lightheaded, pale, and diaphoretic. Denies CP, palp, SOB, or LOC. Vitals: 11:35 110/63, 58, 18, 98% RA -- > 11:45 125/56, 73, 98% RA -- > 11:47 128/66, 68, 20, 99% RA -- > 129/64, 61, 98% RA Pt observed an additional 20mins. Most likely s/sx were associated w/ a vaso-vagal reaction. After ambulation, pt denies symptoms. Pt stable and released from the vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None known
- Andere Medikamente
- None known
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 54,0
- Geschlecht
- M
- Eingang
- 14.12.2021
- Impfdatum
- 07.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: unbekannt
Affective disorder
Angina pectoris
Anticoagulant therapy
Back pain
Bed rest
Catheterisation cardiac abnormal
Chest pain
Chronic left ventricular failure
Coronary artery disease
Coronary artery occlusion
Diabetic nephropathy
Diastolic dysfunction
Echocardiogram
Echocardiogram abnormal
Electrocardiogram abnormal
Glycosylated haemoglobin
Injection site pain
Left atrial dilatation
Symptomtext
5 mins post vaccination pt c/o chest pain. He describes it as sharp, constant, radiating to his left chest and back as well as his left shoulder. He states that it is unremitting, not improved with several of his own nitroglycerin. 911 was called @19:35 Pt then had 3 episodes of vomiting. When EMS arrived, pt was given NTG and ASA and transferred to the ED. Pt reports that morphine helps with the pain. Pt was admitted for further care. Symptoms due to ongoing underlying conditions. Per Discharge Note 12/11 Hospital Problems: 54 y.o. male with ho DM2, HLD, HTN, HFrEF EF 45% and diastolic dysfx 11/2021 at RMC, last nuclear stress test negative 6/2021, CAD s/p DES x 5 (RCA s/p PTCA and thrombectomy of prox RCA stent in 2011 at SCVMC stents in the past with chronic angina who presents with chest pain # Acute on Chronic angina with CAD, challenging case, with innumerable visits for chest pain, negative troponins, refused repeat stress last month; had refused cath in the past as his most recent stent 2019 didn't help his chronic chest pain. Trop flat at 24, EKG non ischemic. LDL 68, HbA1c 8.7. - Cont Aspirin, Plavix, Coreg. - resumed imdur 30 mg daily and ranexa 500mg BID - Cardiology consulted, TTE 12/9: Normal LV systolic function, mild diastolic dysfunction Grade I, severely dilated LA, , - Cardiology recommended stress test but patient refused to have stress test, hence cardiology performed cardiac cath on 12/10 that showed Chronic total occlusion of proximal-Mid RCA with good collaterals, otherwise no obstructive CAD, patent LAD stent -Cardiology recommended: S/p cardiac catheterization -Total occlusion of RCA (chronic) with multiple collaterals -Strict bedrest for 3 hours -No strenuous activity or heavy lifting (>20 lbs) for 1 week -Continue renexa 500mg BID -Continue imdur 30mg daily -Continue PTA aspirin 81mg, plavix 75mg, coreg 25mg -Follow-up in outpatient cardiology clinic with cardiology - pt continued to request morphine solution or norco pills for chest pain, despite educating him that this is not the standard of care for angina and that he needs to take anginal meds per cardiology -No opioids were given at discharge # chronic systolic and diastolic HF, no acute HF symptoms now # HTN - resumed lisinopril, and coreg # DM2 with neuropathy - on gabapentin - LISS and prandial insulin # Mood disorder, - taking wellbutrin and duloxetine Consults Obtained: Cardiology 12/10 Patient is a 54 y/o M with extensive cardiac history (with multiple reported PCIs in the past) along with multiple cardiac RF: DM2, HTN, HLD) and h/o HFrEF (EF 45% and diastolic dysfx 11/2021 at RMC) who presents with acute on chronic angina. He has been seen and RMC 2-3 times in the past month for the same. Low concern for ACS at this time given very low troponin elevation which is stable and no new acute ischemic EKG changes. Suspect his worsening anginal symptoms are in the setting of not taking his appropriate home meds of ranexa and imdur - though his symptoms persist depsite medical managment. Given his symptoms, HEART score of 5 and known CAD/multiple cardiac RF, and relatively unremarkable TTE - he warranted inpatient stress test, though he adamantly refused (stating he almost died), therefore we proceeded with LHC. LHC showed proximal-mid chronic total occlusion at proximal stent edge (multiple stents noted), grade 1 right to right bridging collaterals and grade 2 left to right collaterals. Per cath lab: Patient noted to have vasovagal reaction after access (no sedation given, so not a reaction to sedation). This responded well to normal saline IV bolus, IV phenylephrine, and IV atropine. He reportedly denies any further chest pain s/p catheterization. At this time, plan will be continue aggressive medical management of CAD RF and continue with anti-anginal therapy. Recommendations: -S/p cardiac catheterization today: -Total occlusion of RCA (chronic) with multiple collaterals -Strict bedrest for 3 hours -No strenuous activity or heavy lifting (>20 lbs) for 1 week -Continue renexa 500mg BID -Continue imdur 30mg daily -Continue PTA aspirin 81mg, plavix 75mg, coreg 25mg -Follow-up in outpatient cardiology clinic with cardiology
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: DM2, Obesity, Depression, HLD, HTN, HFrEF EF 45% and diastolic dysfx 11/2021 at RMC, last nuclear stress test negative 6/2021, CAD s/p DES x 5, s/p PTCA and thrombectomy of prox RCA stent in 2011 at SCVMC stents in the past with chronic angina. MI 2 weeks prior to vaccination with 8 stents placed in past
- Andere Medikamente
- ? aspirin 81 MG EC tablet Take 1 tablet by mouth daily. ? atorvastatin (LIPITOR) 40 MG tablet Take 1 tablet by mouth at bedtime. ? blood sugar (FREESTYLE LITE STRIPS) test strip check blood sugars 3 times a day VMC(TI) ? blood-glucose meter
- Allergien
- ondansetron
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 03.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pulmonary thrombosis
Symptomtext
Patient ended in the hospital whit blood clots in both of her lungs; This spontaneous case was reported by a consumer and describes the occurrence of PULMONARY THROMBOSIS (Patient ended in the hospital whit blood clots in both of her lungs) in a 78-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. The patient's past medical history included Clot blood (Patient had a blood clot 16 yeas ago after a 40hs flight.). Concurrent medical conditions included Allergy. Concomitant products included LEVOTHYROXINE SODIUM (SYNTHROID) and ACETYLSALICYLIC ACID (BABY ASPIRIN) for an unknown indication. On 03-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. In November 2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced PULMONARY THROMBOSIS (Patient ended in the hospital whit blood clots in both of her lungs) (seriousness criteria hospitalization and medically significant). The patient was treated with HEPARIN for Adverse event, at a dose of 1 dosage form and APIXABAN (ELIQUIS) for Adverse event, at a dose of 1 dosage form. At the time of the report, PULMONARY THROMBOSIS (Patient ended in the hospital whit blood clots in both of her lungs) had not resolved. Patient was prescribed many blood thinners at the hospital. It was reported that patient was taking an unspecified allergy pill and some herbal medications. Patient has profuse spouts of coffin. Company comment: This case concerns a 78-year-old, female patient with no relevant medical history, who experienced the unexpected event of lung thrombosis, which required hospitalization. The events occurred approximately two weeks after the third dose of mRNA-1273. The rechallenge was not applicable as events occurred after second dose and no further dosing was reported or planned, based on information provided. The medical history of prior blood clots remains a confounder. The benefit-risk relationship of mRNA-1273 is not affected by this report. Most recent FOLLOW-UP information incorporated above includes: On 30-Nov-2021: New serious event (thrombosis)added, seriousness criteria upgraded, patient demographics, vaccination date, batch/lot number, treatment, concomitant medication added, narrative updated; Sender's Comments: Company comment: This case concerns a 78-year-old, female patient with no relevant medical history, who experienced the unexpected event of lung thrombosis, which required hospitalization. The events occurred approximately two weeks after the third dose of mRNA-1273. The rechallenge was not applicable as events occurred after second dose and no further dosing was reported or planned, based on information provided. The medical history of prior blood clots remains a confounder. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pulmonary thrombosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy
- Vorgeschichte
- Medical History/Concurrent Conditions: Clot blood (Patient had a blood clot 16 yeas ago after a 40hs flight.)
- Andere Medikamente
- SYNTHROID; BABY ASPIRIN
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 29.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Anxiety
Arthralgia
Arthritis
Bone pain
Chills
Electric shock sensation
Eye pain
Fall
Fatigue
Feeling abnormal
Feeling cold
Feeling hot
Headache
Nausea
Pain
Paraesthesia
Poor quality sleep
Somnolence
Symptomtext
I got out of bed the morning after the vaccine after having slept/laid down for 12 hours. During that time I was extremely hot but could not break a sweat. My face felt like lava and all my joints were inflamed. There were moments through the night where I'd feel an intense pain in a specific area, it felt like my bone being struck with a hammer. Other times I'd shiver as if my nerves were vibrating. I could feel a throbbing/pulse in my head and ibuprofen seemed to do nothing. My entire body was wrenched in pain, even my eyeballs felt injured. Upon getting out of bed after such a miserable night of supposed rest, I walked up a flight of stairs and had to sit down towards the top because I suddenly felt nauseous. I quickly went back down the stairs hoping I would make it to the bathroom in time. As I lifted up the toilet seat I took a seat on the edge of the bathtub. All I wanted was to wipe off the rim of the bowl with a Clorox towel but even that small task seemed too daunting as I knew my body was starting to turn on me. Throughout my whole being I could feel a wave travel through me as if an electric current had zapped me. Nausea was no longer my concern but rather a dread like something was about to happen but I didn't know what. A pulse hit me which felt similar to when a limb falls asleep and slowly regains circulation however this was all over. The pulse happened twice then my sight started to blur, tunnel vision, as I began to fall backwards into the tub. I never lost consciousness but as I began to feel normal again I instantly felt cold all over. My head felt like I had stuck it in the freezer and chilled me to the bone. As I got out of the tub and snuck a glance in the mirror I was pure white, there was absolutely no color in my face. I went to the living room to rest on the couch and focus on my breathing so as not to have the nausea return. As I did this my whole body felt like it had been asleep, similar to my limb reference earlier, and caused me pain as it regained blood flow. Within 5 minutes I felt normal again but proceeded to have joint pain and fatigue for the rest of the day. On Wednesday I resumed work and my body felt like it had been through an ordeal much like a day of snowboarding and the soreness that comes with it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electric shock sensation
- Hospital-Tage
- -
- Labordaten
- None taken
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None known
- Andere Medikamente
- New Chapter Estrotone (Herbal Hormonal Supplement) No meds
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Presyncope
Symptomtext
Patient had near syncope episode and felt dizzy 2 minutes after first dose of primary series.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Wolff Parkinson White Syndrome
- Andere Medikamente
- None
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 23.11.2021
- Impfdatum
- 16.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Syncope
Symptomtext
10 minutes post vaccination, patient had a syncopal event. Vitals: 133/83, 66, 100%. Patient stable and released to his mother. Patient walked to exit w/RN. Declined wheelchair. Patient had steady gait and left in stable condition at 20:21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: Fainting after blood draws, MGD, s/p pterygium excision and autograft to the left eye.
- Andere Medikamente
- None known
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 23.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Loss of consciousness
Syncope
Symptomtext
Pt. states that after receiving the 3rd Booster dose of Moderna 11/05/2021, started experiencing symptoms 11/06/2021 of fainting (shortly after waking, fainted resulting in 3 hours unconsciousness). Unknown status of symptom. No noted Primary visit/communications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Loss of consciousness
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Baby Aspirin
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 21,0
- Geschlecht
- M
- Eingang
- 20.11.2021
- Impfdatum
- 16.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chest pain
Dyspepsia
Hypoaesthesia oral
C-reactive protein
Electrocardiogram abnormal
Myocarditis
Troponin
Symptomtext
Constant numbing/dull chest pain. occasional sharp pains in all areas of chest, occasional heart burn feelings as well as sharp pain in the heart.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Myocarditis
- Hospital-Tage
- -
- Labordaten
- Blood drawn and examined to look for a specific enzyme in the blood.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Flushing
Hyperhidrosis
Syncope
Symptomtext
1min post vaccination, pt was feeling dizzy on walk over to observation. Pt was assissted to the ground and had a syncopal episode. Pt was flushed and sweating. Pt assissted to wheelchair once alert and taken to medical tent. Syncopal episode only lasted seconds. Pt given juice and crackers remains clammy and flushed but states that she is feeling much better. Pt states that her BP normally runs low. After 15mins of observation, Vital signs and pt states that she feels better and is comfortable going home. Pt stable w/ strong/steady gait upon leaving. Vitals: 95/53, 68, 14 -- > 97/57, 74
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: Generalized anxiety disorder, hx of eating disorder, atopic dermatitis/eczema
- Andere Medikamente
- Medications: Mirena IUD Triamcinolone 0.1% cream BID for eczema flares Fluoxetine 60mg daily
- Allergien
- Allergies: PCN
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 17.11.2021
- Impfdatum
- 13.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pain in extremity
Thrombosis
Ultrasound scan abnormal
Symptomtext
Blood clot in left arm. Woke up with arm pain in the same arm the shot was given 3 days after the shot. The pain was on the underside of my arm. Went to the drs and had an ultrasound done and a blood clot was found. They started me on blood thinners.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Thrombosis
- Hospital-Tage
- -
- Labordaten
- An ultrasound was performed on 11/16/2021 which found the blood clot in my left arm.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Factor II gene mutation
- Andere Medikamente
- None
- Allergien
- Amoxicillin and shellfish
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Dysstasia
Fatigue
Headache
Influenza like illness
Pain in extremity
Syncope
Symptomtext
As with 2nd dose, the day of was fine, following day horrible. Could not stand because of extreme dizziness. Fainted both for 2nd and 3rd doses. Lasted all day. Second day like having mild flu. Third day better, still some arm pain, fatigue, headache.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism
- Andere Medikamente
- Levothyroxine .088mcg Alendronate 70mg Calcium citrate 900 mg Vitamin D 1500 IU Zinc 7 mg Copper .75 mg Manganese 2 mg
- Allergien
- Ampicillin Nickel
- Vorherige Impfungen
- Moderna 2nd dose, 3/29/21, age 65. Same adverse event as previously described
- Staat
- OH
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 09.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Head injury
Syncope
Vomiting
Symptomtext
Spouse called to report vomiting, the patient had told her he had fainted, and hit his head.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Answered no to the screening question, though when spouse called to report event stated he had been sick for about a week.
- Vorgeschichte
- Presumed COPD
- Andere Medikamente
- Unknown
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 07.11.2021
- Impfdatum
- 07.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Cold sweat
Feeling hot
Posture abnormal
Presyncope
Symptomtext
The patient's husband motioned for me to come out to the post vaccination area. This was about 10 minutes after the patient received her first Moderna Covid 19 vaccine. Patient's husband motioned for me to come out and help with his wife who had received a COVID vaccine about 10 minutes earlier. He said she's about to pass out. He said we knew this was going to happen that's why I came with her. He said she always passes out. Said she did every time she received a flu shot and therefore she was expecting it. Technician announced code white and another tech brought an ice pack out for us. He held her head and I held her torso up in the chair so she wouldn't slump down in the chair and slide out. She felt a little clammy so we got an ice pack for the back of her neck and we asked her if she felt hot and she said yes. She had her eyes closed but she would always respond when we spoke to her. She slumped over again and them came back to but was just too weak to really open her eyes or hold herself up. She responded to us whenever we would ask her any questions. Her husband asked her if she wanted a drink of water so we gave her an unopened bottle of water and she could hold it herself and drink herself. She started perking up after that and even started eating her hot balls from her purse. She stayed with us for about 30 to 45 minutes and said she felt okay now. Two associates in the store (-claims associate) walked out with the patient and her husband to make sure didn't have any spells on the way to the car. The patient hugged me before she left and said that was the best shot she ever got and said she really appreciated us tending to her and she would be back to get her 2nd shot here.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Presyncope
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Patient stated she has no other illnesses at the time of vaccination.
- Vorgeschichte
- NO chronic or long-standing health conditions per patient and husband.
- Andere Medikamente
- Patient stated she doesn't take any medication of any kind
- Allergien
- No known drug allergies
- Vorherige Impfungen
- Patient said she passed out after every flu shot she had ever gotten. Her last flu shot was 10 years ago.
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Decreased appetite
Fatigue
Hemiparesis
Immediate post-injection reaction
Interchange of vaccine products
Movement disorder
Syncope
Symptomtext
Member previously received Jansen as first dose. Member requested and Received Moderna booster at 1206. Immediately after vaccination, member complains of being very tired and weak. RN was called to station. Patient says she cannot get up and she needed to just sit there. Suddenly she went limp and was held up by the RN. Member always remained conscious and oriented, just weak. Nurse assessed function and strength of each limp before wheelchair was brought over. Patient was able to pivot to wheelchair. Member was then able to transfer from wheelchair to gurney. 1210 Vitals 143/93 (77) BP 120 HR sat 99 Member's husband was called to the bedside and stated that she has not eaten anything that day. Pt drank 8oz juice and a few pieces of graham crackers. Upon reassessment of limbs, starting with toes, patients started having decreased movement in left toes, feet, and arm. Right side had full strength. 1213 MD Stat (Hospital Urgent Response team consisting of RNs, MD, and Security) 1216 MD stat arrived and conducted a full assessment. Dr. Recommended patient go to the the ER because the members left sided weakness. 2L o2 started for high BP 1217 ED called 1230 RN started PIV 1232 EMS called Member transferred out at 1240
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Syncope
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hx of High Blood Pressure and Depression
- Andere Medikamente
- None
- Allergien
- Phenergen
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 09.10.2023
- Impfdatum
- 17.11.2021
- Beginn
- 01.01.2022
- Tage bis Beginn
- 45,0
- Dosis
- 1
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Breakthrough COVID-19
Dyspnoea
Feeling abnormal
Feeling of despair
Hypersensitivity
Insomnia
Insurance issue
Loss of employment
Loss of personal independence in daily activities
Malaise
Paranasal sinus inflammation
Rhinorrhoea
Sinus disorder
Sleep disorder
Symptomtext
I had Covid before being vaccinated, it was mild, felt like a small cold or allergic reaction. After getting both doses of the vaccine, I later got Covid and was sicker than I had ever been in my life, to the point where I literally thought I was going to die. At this time is when the allergy and sinus problem came into play in a severe manner. Allergy pills, Dayquil, pseudoephedrine, Mucinex, vitamins, nothing helps anymore. It seems to get worse; I suffer daily and half the time I lose sleep because I either cannot breathe, or I have to lay in the weirdest positions just to be able to breathe or not have not run down my face and soak my pillow. Half of my days consist of toilet paper up my nostrils just so I can get through my day without stopping to blow my nose. I was working remotely, and now laid off and desperately looking for work, and this has affected my life so badly I do not think I can find an On-site job due to the fact I will not be able to blow my nose every 2 minutes or walk around appropriately with toilet paper shoved up my nose. I am miserable daily and have no hope for my future. This is no way to live life.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- I went to the doctor once about a year ago and they said to just take over the counter allergy medication to fight the inflammation in my sinus. I had already been taking it daily with little to no relief. I have no insurance anymore because of being laid off so I cannot get testing. Nothing in my life, diet, or otherwise has changed. Only thing different is that I was vaccinated and got Covid 10 times worse after along with severe allergy and sinus issues.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Vitamin D3
- Allergien
- MILD allergies to some cats and dogs and overwhelming amounts of pollen.
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 23.03.2023
- Impfdatum
- 10.11.2021
- Beginn
- 01.03.2022
- Tage bis Beginn
- 111,0
- Dosis
- 3
- Route/Site
- SYR / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
COVID-19
Infusion
Malaise
Migraine
Pyrexia
SARS-CoV-2 test positive
Sinusitis
Taste disorder
Symptomtext
My COVID-19 symptoms started on 03/2022 in the morning, I had sinus infection, fever, loss of taste, and migraine headaches. Then next morning I took a home COVID-19 test which was positive. I called my doctor and informed him about the test. He scheduled an appointment to the hospital to get an infusion because of my heart condition. Now I have a loss of taste. Sometimes it's too sweet and sometimes I don't even feel anything. It's been happening for the last 12 months. I can't feel any taste it's so different now. It comes and goes. Sometimes the taste will come on and sometimes its completely gone. The sweet and salty taste is so dominant.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Migraine
- Hospital-Tage
- -
- Labordaten
- MAR2022 COVID-19 test positive
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- High Cholesterol; Heart Disease
- Andere Medikamente
- Rosuvastatin; aspirin; FLONASE
- Allergien
- Seasonal allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 27.12.2022
- Impfdatum
- 16.01.2021
- Beginn
- 09.04.2021
- Tage bis Beginn
- 83,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: unbekannt
Burning sensation
Electromyogram normal
Magnetic resonance imaging normal
Magnetic resonance imaging spinal normal
Nerve conduction studies normal
Pain in extremity
Paraesthesia
Symptomtext
Bil burning tingling pain of both plantar surface of both feet starting in April. Symptoms worsened after 4th injection on 10/01/2022 of the Pfizer bivalent vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- NCV and EMG ruled out large fiber neuropathy on 11/30/2022. MRI of lumbar and bil ankles on 11/23/2022 and 11/28/2022 also ruled out lumbar radiculopathy and tarsal tunnel syndrome
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Microgestin (Hailey) 1.5/30
- Allergien
- Bactrim, tree nuts, cat dander
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 05.12.2022
- Impfdatum
- 04.12.2021
- Beginn
- 17.09.2022
- Tage bis Beginn
- 287,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Dyspnoea
Fatigue
Illness
Pyrexia
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
I received my first Moderna booster for COVID-19 on 12/04/2021. In the early morning of 9/17/2022, I had a fever of about 100 degrees. I then took a PCR test and got a positive result. I was abroad at the time, so I went to a website that provides medical guidance to travelers. The doctor I spoke to advised me to treat my symptoms with paracetamol. I took the paracetamol regularly from then on. Whenever I took it, my fever was reduced to about 98 degrees. However, whenever the medicine wore off, the fever would reach about 99 again. This pattern lasted for about 4 days before I stopped getting the fevers. Around 9/21/2022, I started developing fatigue and shortness of breath. The fatigue and shortness of breath lasted until around 9/21/2022. I tested myself regularly with antigen tests during my illness and had a positive result every day until 9/24/2022, which is when I finally got a negative result. On 9/29/2022, I took a PCR test and got a negative result. I didn't feel fully recovered until 10/3/2022, because I still have residual fatigue.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 9/17/2022 PCR test positive result; 9/18/2022-9/23/2022 home antigen tests positive results; 9/24/2022 home antigen test negative result; 9/29/2022 PCR test negative result.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- None.
- Allergien
- None.
- Vorherige Impfungen
- After each of my Moderna injections for COVID-19, I developed a fever of 100. The fevers lasted for about 24 hours before they s
- Staat
- MI
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 04.11.2022
- Impfdatum
- 04.02.2021
- Beginn
- 09.09.2022
- Tage bis Beginn
- 582,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Dyspnoea
Laboratory test abnormal
SARS-CoV-2 test positive
Symptomtext
09/09/22 presents to ED for "abnormal labs, shortness of breath". PMHx of ", cardiac arrest, anoxic brain injury"
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- 09/09/22 SARS-CoV-2 (COVID-19) by NAA detected
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 48,0
- Geschlecht
- F
- Eingang
- 30.09.2022
- Impfdatum
- 04.11.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 30,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arrhythmia
Arteriospasm coronary
Axillary pain
Blood pressure measurement
Breast inflammation
Cardiac disorder
Constipation
Coronary artery occlusion
Dizziness
Dyspnoea
Enzyme level test
Gastrointestinal disorder
Hypertension
Inflammation
Lipids
Lymphadenitis
Lymphadenopathy
Mammogram
Symptomtext
A year-round of hearth problems; Vertigo; Cannot bend over or look up; Uterus was 6 times bigger than normal; Prolapse; Fibroids; inflammation of her left breast; pain; Gastrointestinal problems; Major constipation; Dizziness; Armpit hurts; Swelling of the lymph nodes in her armpit and neck; She also had an inflammation of the lymph nodes on her face on the left side; 4 types Arrhythmias (PAC, PVC, SVT and VTac); 50% right coronary blockage related with inflammation; Quivering in arteries; High Blood Pressure; Shortness of breath; 50% right coronary blockage related with inflammation, Inflammation in the cartilage between her ribs.; This spontaneous case was reported by a patient and describes the occurrence of ARRHYTHMIA (4 types Arrhythmias (PAC, PVC, SVT and VTac)), CORONARY ARTERY OCCLUSION (50% right coronary blockage related with inflammation) and ARTERIOSPASM CORONARY (Quivering in arteries) in a 48-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Concomitant products included METOPROLOL for Arrhythmia and Shortness of breath, LOSARTAN for Blood pressure high, CARISOPRODOL (MIO RELAX [CARISOPRODOL]), SODIUM PICOSULFATE (DULCOLAX [SODIUM PICOSULFATE]) and SENNOSIDE A+B (SENOKOT) for Constipation. On 04-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 04-Dec-2021, the patient experienced ARRHYTHMIA (4 types Arrhythmias (PAC, PVC, SVT and VTac)) (seriousness criterion medically significant), CORONARY ARTERY OCCLUSION (50% right coronary blockage related with inflammation) (seriousness criterion medically significant), ARTERIOSPASM CORONARY (Quivering in arteries) (seriousness criterion medically significant), HYPERTENSION (High Blood Pressure), DYSPNOEA (Shortness of breath) and INFLAMMATION (50% right coronary blockage related with inflammation, Inflammation in the cartilage between her ribs.). On an unknown date, the patient experienced CARDIAC DISORDER (A year-round of hearth problems), VERTIGO (Vertigo), MOBILITY DECREASED (Cannot bend over or look up), UTERINE ENLARGEMENT (Uterus was 6 times bigger than normal), PROLAPSE (Prolapse), UTERINE LEIOMYOMA (Fibroids), BREAST INFLAMMATION (inflammation of her left breast), PAIN (pain), GASTROINTESTINAL DISORDER (Gastrointestinal problems), CONSTIPATION (Major constipation), DIZZINESS (Dizziness), AXILLARY PAIN (Armpit hurts), LYMPHADENOPATHY (Swelling of the lymph nodes in her armpit and neck) and LYMPHADENITIS (She also had an inflammation of the lymph nodes on her face on the left side). The patient was treated with DOXYCYCLINE for Pain, at an unspecified dose and frequency. At the time of the report, ARRHYTHMIA (4 types Arrhythmias (PAC, PVC, SVT and VTac)), ARTERIOSPASM CORONARY (Quivering in arteries), HYPERTENSION (High Blood Pressure), DYSPNOEA (Shortness of breath), INFLAMMATION (50% right coronary blockage related with inflammation, Inflammation in the cartilage between her ribs.), CARDIAC DISORDER (A year-round of hearth problems), VERTIGO (Vertigo), MOBILITY DECREASED (Cannot bend over or look up) and DIZZINESS (Dizziness) had not resolved and CORONARY ARTERY OCCLUSION (50% right coronary blockage related with inflammation), UTERINE ENLARGEMENT (Uterus was 6 times bigger than normal), PROLAPSE (Prolapse), UTERINE LEIOMYOMA (Fibroids), BREAST INFLAMMATION (inflammation of her left breast), PAIN (pain), GASTROINTESTINAL DISORDER (Gastrointestinal problems), CONSTIPATION (Major constipation), AXILLARY PAIN (Armpit hurts), LYMPHADENOPATHY (Swelling of the lymph nodes in her armpit and neck) and LYMPHADENITIS (She also had an inflammation of the lymph nodes on her face on the left side) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 04-Dec-2021, Blood pressure measurement: High. On an unknown date, Enzyme level test: Elevated. On an unknown date, Lipids: Elevated. On an unknown date, Mammogram: Inflammation in the cartilage between ribs.. On an unknown date, White blood cell count: Elevated. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Did a stress test, echocardiogram and arteriogram. He said this blockage was not due to build up in the artery. A lipid control specialist who gave her 2 medications and is about to give her a 3rd one. Also, after the booster she had perimenopausal ultrasound and had to perform a hysterectomy. Performed the surgery on 17Aug2022. Uterus weighted 300 grams instead of 60 grams. Patient had no myocarditis or pericarditis previously and also never tested positive for COVID 19: No Company Comment: This is a spontaneous case concerning a 48-year-old female patient with no reported medical history, who experienced the unexpected, serious (medically significant) adverse event of special interest of Arrhythmia and the unexpected, serious (medically significant) events of Coronary artery occlusion and Arteriospasm coronary, 30 days after receiving the third dose of mRNA-1273 vaccine. The patient developed shortness of breath and underwent stress test, echocardiogram and arteriogram which showed 4 different types of Arrhythmias (PAC, PVC, SVT and VTac), quivering of arteries and 50% right coronary blockage. The patient was treated with Metoprolol and medications for lipid control. The outcome of the events unknown at the time of the report. The benefit-risk relationship of mRNA-1273 is not affected by this report. This case was linked to MOD-2022-649984, MOD-2022-649986 (Patient Link). Sender's Comments: This is a spontaneous case concerning a 48-year-old female patient with no reported medical history, who experienced the unexpected, serious (medically significant) adverse event of special interest of Arrhythmia and the unexpected, serious (medically significant) events of Coronary artery occlusion and Arteriospasm coronary, 30 days after receiving the third dose of mRNA-1273 vaccine. The patient developed shortness of breath and underwent stress test, echocardiogram and arteriogram which showed 4 different types of Arrhythmias (PAC, PVC, SVT and VTac), quivering of arteries and 50% right coronary blockage. The patient was treated with Metoprolol and medications for lipid control. The outcome of the events unknown at the time of the report. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arrhythmia
- Hospital-Tage
- -
- Labordaten
- Test Date: 20211204; Test Name: Blood Pressure; Result Unstructured Data: High; Test Name: liver enzymes; Result Unstructured Data: Elevated; Test Name: Lipids; Result Unstructured Data: Elevated; Test Name: mammogram; Result Unstructured Data: Inflammation in the cartilage between ribs.; Test Name: White blood cells count; Result Unstructured Data: Elevated.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- LOSARTAN; METOPROLOL; MIO RELAX [CARISOPRODOL]; DULCOLAX [SODIUM PICOSULFATE]; SENOKOT
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 24.08.2022
- Impfdatum
- 02.12.2021
- Beginn
- 02.02.2022
- Tage bis Beginn
- 62,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthropathy
Condition aggravated
Gait disturbance
Impaired self-care
Loss of personal independence in daily activities
Mobility decreased
Vertigo
Wheelchair user
Symptomtext
He got his vaccine, exactly 2 months later he was lying in bed, opened his eyes and felt like he was in a cement mixer. The whole room was moving from left to right. He closed his eyes and the feeling went away, but as soon as he opened his eyes again the room was spinning again. He had to stay in bed for a while, he was alone and had no family to take care of him. He then had some healthcare workers come and he was not able to take care of himself and do his chores. The spinning stopped after about a year, and took him a while to adapt to it. He had to use a wheelchair to get around, he can walk some but cannot walk for long. His knee issue he had as a child then started up again due to his loss of not using his leg. He can get down 6 steps to get to his truck, but has to be very careful.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- High blood pressure, high cholesterol, prostate cancer, multiple surgeries.
- Andere Medikamente
- 5 pills in the morning and 6 in the afternoon.
- Allergien
- Penicillin.
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 88,0
- Geschlecht
- M
- Eingang
- 19.07.2022
- Impfdatum
- 08.11.2021
- Beginn
- 15.07.2022
- Tage bis Beginn
- 249,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19 pneumonia
Dehydration
Diabetes mellitus inadequate control
Fall
Symptomtext
Pt presented with covid pneumonia, uncontrolled diabetes, dehydration and multiple falls. Pt given iv fluids and labs monitored. pt discharged home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- DM, dementia, Htn, bph, glaucoma,
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 07.06.2022
- Impfdatum
- 01.11.2021
- Beginn
- 23.04.2022
- Tage bis Beginn
- 173,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: ja
Erholt: nein
Activated partial thromboplastin time shortened
Atelectasis
Blood chloride increased
Blood urea nitrogen/creatinine ratio
Chest X-ray abnormal
Chest pain
Differential white blood cell count
Dyspnoea
Electrocardiogram ST segment elevation
Fatigue
Full blood count
International normalised ratio
Lung infiltration
Metabolic function test
Mycoplasma test positive
Procalcitonin
Prothrombin time
Speech disorder
Symptomtext
On April 23, 2022 started having shortness of breath and fatigue. By the 25th chest pain and tachycardia throughout week. Being followed by PCP who ordered cardiac monitor. Symptoms became emergent on April 30, 2022. Severe shortness of breath led to calling EMS. From April 23rd to April 30th all symptoms included shortness of breath, chest pain, tachycardia, fatigue, and trouble speaking sentences due to shortness of breath.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- CMP 4/30/22-BUN/Creatinine Ration 13 APTT 4/30/22-21.8 Procalcitonin 4/30/22-0.07 CBC w/ Diff 4/30/22 WBC's 10.9 Protime-INR 4/30/22 INR 1/01 Chest Xray 4/30/2022 Left basilar atelectasis versus infiltrate BMP 5/1/22 Chloride 108 Mycoplasma Pneumoniae Positive on 5/1/22 EKG 5/3/22 slight ST elevation
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Pepcid over the counter
- Allergien
- Aspirin, chocolate, tree nuts, MSG
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 03.05.2022
- Impfdatum
- 03.11.2021
- Beginn
- 23.03.2022
- Tage bis Beginn
- 140,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Chest X-ray normal
Cough
Dyspnoea
Fatigue
Hypophagia
Inappropriate schedule of product administration
SARS-CoV-2 test positive
Symptomtext
COVID related hospitalization after vaccination with Moderna vaccine series + booster (11/3/2021, 2/20/2021, 1/22/2021). Moderna given 11/3/2021 left arm, lot 066F21A 2/20/2021 lot 006M20A 1/22/2021 lot 029L20A Admitted 3/23/22 Discharged 3/26/22 Positive covid test 3/23/22 Presented with generalized fatigue, cough and shortness of breath for 7-8 days prior to admission. Was treated outpatient with Levaquin 10-day therapy (suppose to finish in 2 days), but continued to have reduced oral intake and worsening fatigue and cough so came to hospital. Chest X-ray with no acute abnormalities On room air on admission 3/23/22. Overnight required oxygen and dexamethasone (Decadron) 6mg daily was started 3/24/22. Weaned back to room air in the afternoon on 3/24/22 but then required oxygen overnight. Off of oxygen for 24hrs prior to discharge. Last dose of Decadron 3/26. No steroids after discharge. Given guaifenesin 600mg for 7 days of therapy after discharge.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Coronary artery disease Diabetes mellitus Hypertension Peptic ulcer disease NSTEMI Neurogenic bladder BPH
- Andere Medikamente
- Cyanocobalamin 1000mcg Acetaminophen 500mg prn Albuterol inhaler prn Allopurinol Amlodipine Aspirin 81mg Atorvastatin 80mg Cephalexin 250mg daily Vitamin D3 5,000 unit Cranberry 500mg Donepezil 10mg Ferrous gluconate 240mg Finas
- Allergien
- nitrofurantoin, imiquimod
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 30.10.2021
- Beginn
- 23.01.2022
- Tage bis Beginn
- 85,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Ageusia
Anosmia
COVID-19
Condition aggravated
Exposure to SARS-CoV-2
Pyrexia
Rhinorrhoea
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Throat irritation
Transient global amnesia
Symptomtext
On day 10 after vaccine I had an episode of Trans global Amnesia. These are usually triggered by elevated heart rate or intense physical activity. This episode lasted about 15 minutes. COVID-19 infection was due to exposure to daughter and grandson, they were symptomatic in the few days prior to my testing positive. Day 1 I had a scratchy throat. Within 24 hours I had a fever 99.6 at the highest and a runny nose. The fever lasted 3 days. On the 8th day I lost my sense of smell and taste, but they returned after 2 days.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- On 1/22 PCR was negative, at COVID-19 test 1/25 positive.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Episodes of Trans Global Amnesia
- Andere Medikamente
- Restasis, Spironolactone, Aspirin, R-Alpha Lipolic Acid, Berberine, Chromium Colinate, D Complex, Omega3 Inflammation Balance, Plant Spiral, Multivitamin
- Allergien
- Sulfa; Gluten Intolerant; Nickel
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 29.03.2022
- Impfdatum
- 11.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Arthritis
Axillary pain
Blood urine present
Condition aggravated
Fatigue
Haemorrhage
Headache
Malaise
Pain
Pyrexia
Sinusitis
Urinary tract infection
Urine analysis abnormal
Vaccination site erythema
Vaccination site swelling
Vaccination site warmth
Symptomtext
I had a significant headache that evening. Vaccination site was red raised and warm to the touch. I also had fever chills during all of this. It was more than 5 inches in diameter I had significant underarm pain that radiated, and it lasted for 5-7 days which was shocking. I had fatigue and overall pain that was so much more than dose 1 & 2. I just wasn't well at all. Sunday after going through all this I go to urgent care, and I was diagnosed UTI and a sinus infection. Blood in my urine (significant amount) and they both hit me sudden. I told them at the urgent care, and they couldn't tell me anything. What's been long standing is inflammation in my joints no breathing issues, but all my joints were in so much pain. So much inflammation I must now see a rheumatologist and I have never had these issues before. Less than a month 6 weeks max I had to go back my PCP and I was bleeding again. They did a culture and the finding wasn't bacterial. My doctor then put me on something else did work and I was in fact healed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Urine test results stated nonbacterial
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Insulin resistance; Asthma
- Andere Medikamente
- Metformin 750 ER; Aldactone; LIVALO; Magnesium; Omega 3; Vitamin D3; B12; FLONASE; Zinc
- Allergien
- Peanuts; Sulfa; Seasonal Allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 11.03.2022
- Impfdatum
- 22.12.2021
- Beginn
- 05.01.2022
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: ja
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Atrial fibrillation
Cardiac monitoring
Injection site pain
Injection site swelling
Insomnia
Paraesthesia
Symptomtext
On the first 3 days had swelling and pain in right deltoid (no erythema or fluctuance) making it very difficult to sleep. Things calmed down but starting 1/5/22 developed paresthesias in my right arm and hand. On 2/15/22 I had an episode of new-onset AFib which prompted an ED visit and which resolved with metoprolol. The question of vaccine-induced myocarditis was raised; on a Zio and will have an echo soon
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- See above, Zio and pending echo
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- thyroid nodule/parathyroid adenoma
- Andere Medikamente
- -
- Allergien
- Flu vaccine ADR, NSAIDs
- Vorherige Impfungen
- Flu vaccine, multi-dermatomal neuritis
- Staat
- KY
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 11.03.2022
- Impfdatum
- 11.11.2021
- Beginn
- 16.02.2022
- Tage bis Beginn
- 97,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: ja
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
COVID-19 pneumonia
SARS-CoV-2 test positive
Symptomtext
hospitalized on 2-16-22 for COVID pneumonia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 pneumonia
- Hospital-Tage
- 16,0
- Labordaten
- tested positive for COVID-19 on 2-16-22
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- Hypertension, COPD, Diabetes, Cardiovascular Disease
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 28.02.2022
- Impfdatum
- 06.01.2022
- Beginn
- 06.01.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chest X-ray normal
Chest discomfort
Chest pain
Electrocardiogram normal
Fatigue
Hypertension
Loss of personal independence in daily activities
Symptomtext
About little over a week (1/18/2022) after 3rd dose of moderna, I started experiencing chest pains, tightness, heaviness in the chest, very tired on days that symptoms are more prevelant. Feeling of high blood pressure, lightheaded, sometimes little dizzy. The symptoms also come in waves, some days its much lighter and some days its very painful to the point I feel shooting aches in other parts of the body. It is now over 7 weeks from vaccine and about 6 weeks from first symptoms and nothing is improving to the point I used to function.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- 1/31/22 Blood pressure check normal, ecg normal, 1/24/22 chest xray normal
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- Birthcontrol
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 06.02.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chest discomfort
Dyspnoea
Nausea
Symptomtext
Client reported pressure on her chest and shortness of breath to EMT. RN responded. At 4:50PM the client reported feeling nausea and pressure on her chest. Vitals obtained at 4:51PM were as follows: BP 146/86, HR 79, O2 99%. At 4:52PM the client was provided juice and stated she still felt pressure on her chest. The client began drinking the juice. The client stated she last ate at 8:00 AM. The client reported a history of gastritis. Vitals obtained at 5:00PM were as follows: BP 146/90, HR 85, O2 98%. The client stated the pressure on her chest was improving and denied any current nausea. The client declined an warmness on her chest. The client denied any allergies or current medications. Vitals obtained at 5:10PM were as follows: BP 130/86, HR 80, O2 99%. The client reported less pressure on her chest, denied any shortness of breath, chest pain. Client ate two crackers, finished the juice, and began drinking water provided by staff. The client reported that she experienced body aches, a headache, and fever the day after she received her second COVID vaccine Moderna. The client stated those symptoms lasted one day and improved with taking Tylenol. Vitals obtained at 5:20PM were as follows: BP 136/84, HR 72, O2 99%. The client stated the pressure was almost gone, denied any nausea, chest pain, or warmness. RN educated the client regarding s/s of anaphylaxis and when to seek EMS, the client voiced understanding of this education. The client ambulated out of the vaccination site at 5:24PM unassisted with a steady gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dyspnoea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 10.01.2022
- Impfdatum
- 17.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Headache
Neck pain
Pain in extremity
Paraesthesia
Symptomtext
The client did not report any symptoms during the 30 minute observation period. As the client was leaving the vaccination site, the client reported, "tingling in my genitals, headache, arm ache, and a neck ache" to RN.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- diverticulitis and alopecia
- Andere Medikamente
- Vitamin D
- Allergien
- allergy to penicillin but did not know the reaction that occurred, panic attacks with Vicodin and "feeling worse" after taking sulfa medications
- Vorherige Impfungen
- The client received the 1st COVID vaccine Moderna (Lot #011F21A and expiration date 01/19/2022) on 10/17/21. The client notified
- Staat
- TN
- Alter
- 34,0
- Geschlecht
- M
- Eingang
- 04.01.2022
- Impfdatum
- 04.12.2021
- Beginn
- 07.12.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test normal
Chest pain
Chills
Electrocardiogram normal
Fatigue
Pain
Palpitations
X-ray normal
Symptomtext
Heart Palpitations, fatigue and chest pain starting after 4 hour stint of severe chills and body aches 3 nights after administration of the 3rd shot (moderna). Chest pain and heart palpitations have remained constant over the past four weeks. Seeking follow up with cardiologist next week.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- Emergency room EKG, blood work and xray appear normal after emergency room visit on 12/29/2021
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Montelukast Axelastine nasal Spray Sublingual Allergy Drop Therapy Cetirizine
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 74,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Aphasia
Blood test
Confusional state
Eye pain
Hypertension
Magnetic resonance imaging head
Muscle spasms
Symptomtext
Bad leg cramps on 12 -21 then on 12-22 could not get my words out and was very confused. Blood pressure was 202 /78 12-23 still confused and went to Emergency room. Left eye aches and blood pressure high. Still can't get my words out.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypertension
- Hospital-Tage
- -
- Labordaten
- They did MRI of my brain did bloodwork checked my eyes.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Diabetes
- Andere Medikamente
- Metformin. Preservision vitamins cardillo baby aspirin crestor synthroid. Insulin vitamin d
- Allergien
- Zocor
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 45,0
- Geschlecht
- F
- Eingang
- 30.12.2021
- Impfdatum
- 22.12.2021
- Beginn
- 22.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Anxiety
Chest pain
Cough
Symptomtext
@9:47 Pt reported chest pain5/10, anxiety and coughing. V/S 115/71, 78, 15, 97.9F 100% MAR called at 9:51 am for patient complaining of chest pain 2/10 after receiving Moderna Booster vaccine at 0905 am. V/S: BP-113/75, HR- 78, RR-20. O2sat- 100%, MD ordered to place patient on trendelenburg position for 15 minutes, patient tolerated trendelenburg position well, continued to observed patient, patient is A/Ox4, MAE, talking in full sentences, no signs and symptoms of sob or discomfort, patient denies any dizziness, V/S 9:56 am: BP-107/67, HR-76, RR-20, O2 sat-100% RA 9:57 am: patient denies any chest pain, chest pain, 0/10. 10:08 am: Patient stable, discharged home. MD recommends pt lay down for next vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 29.12.2021
- Impfdatum
- 26.11.2021
- Beginn
- 26.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Crying
Injected limb mobility decreased
Injection site pain
Loss of personal independence in daily activities
Pain
Product administered at inappropriate site
Symptomtext
Both shots were given too high on each shoulder. The flu shot/left arm injection missed the deltoid muscle and went far too high, into the joint. Severe pain moving the arm within hours, leaving patient in tears and unable to perform regular household tasks. Over time, symptoms improve somewhat then return. One month later, patient still has difficulty bathing and dressing. Anything requiring the shoulder to rotate forward and apply pressure to lift or pull causes severe pain. The arm cannot be lifted all the way overhead.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injected limb mobility decreased
- Hospital-Tage
- -
- Labordaten
- None yet, seeking medical care within the week
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Generalized anxiety
- Andere Medikamente
- Escitalopram Propranolol Focalin Allegra
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 48,0
- Geschlecht
- M
- Eingang
- 15.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 14,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Condition aggravated
Hyperhidrosis
Malaise
Pyrexia
Rash
Urticaria
Symptomtext
Full body rash / hives that has moved around the body from head to toe. Progressing throughout the time period.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- Visual Exam
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- Chills, sweats, fever, malaise after 2nd and 3rd doses
- Staat
- WA
- Alter
- 33,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 21.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Chest X-ray normal
Chest discomfort
Chest pain
Electrocardiogram normal
Headache
Palpitations
Symptomtext
Tightness and pain (dull and sharp) in chest. Racing heart. 3 weeks so far and still going. Headache for 10 days straight.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chest pain
- Hospital-Tage
- -
- Labordaten
- EKG, x ray of lung, and blood work all appeared normal.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- None
- Andere Medikamente
- Vitamin D, IUD (Mirena)
- Allergien
- Bactrim, Amoxicillin, Flonase
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 77,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 03.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Asthenia
Blood pressure abnormal
Diarrhoea
Headache
Mobility decreased
Nausea
Pyrexia
Symptomtext
Symptoms began 12/4/2021. Headache for 5 days, Tylenol did not help, Nausea, Diarrhe for 5 days, too weak to get out of bed, , fever, Came to local Health Dept 12/8/2021 Bp 170/110. I referred to her Primary care Dr.. I called to check on her today 12/9/2021. She said Dr said her bp was wnl now and did no changes to her meds.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Blood pressure med (pt. unsure of name).
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- IN
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Condition aggravated
Fear
Feeling abnormal
Migraine
Mobility decreased
Pain
Sitting disability
Symptomtext
SEVERE aches and chilling. Severe migraines. I have never felt this bad in my life. Seriously contemplated going to ER and I have not been to an ER for 25 years. The only reason I didn't go is because I was unable to sit up for that long of a period to get there and get checked in. I am scared if I have to get another booster at some point. This lasted for 48 hours. I was unable to get out of bed except to occasionally going to bathroom.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Synthroid
- Allergien
- sulfa
- Vorherige Impfungen
- Ran 103 fever for 3 days after second moderna dose. Aches and pains but no where near this.
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Hypoaesthesia oral
Paraesthesia oral
Somnolence
Symptomtext
Approximately 10 minutes after vaccination,(2:20 PM on 12/2/21) patient began experiencing lip tingling and tongue began to feel numb. 2:35 PM Dr. notified and checked patient, MD ordered Benadryl 50 mg which was given at 2:38 PM orally. 2:48 PM patient notes tongue still feels swollen but is feeling better, 2:55 PM vital signs taken - breathing fine, feeling like tongue is less swollen. Lips are not tingling. T 97.2, BP 119/68, P-72, R-16, 02 97% r/a. 3:00 PM DR. advised patient to wait an additional 20 minutes. 3:15 PM patient feeling a little better, though sleepy. 3:20 Vital signs taken: R -20, 02 96% on ra, P-71, BP 119/72. Tongue less swollen, feeling sleepy. Patient was allowed to go home, accompanied by mother who will drive them. Encouraged to call back if further problems. Patient was contacted the following day and states she is doing OK. Per Dr. advice, patient instructed to be sure to take 50 mg Benadryl PO 1/2 hour prior to coming in for second Moderna vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia oral
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- Not known
- Vorgeschichte
- Irritable bowel syndrome, Ulcerative colitis, Hyperprolactinemia
- Andere Medikamente
- Nitroglycerin topical 2%, KCL 8 MEQ, Albuterol, Paroxetine HCL 30 mg., Metoclopramide HC 5 mg, Loperamide HCL 2 mg. prn, Ondansetron, HCL 8 mg. Norethin-Ace-Eth Estrad-FE1-20 Cyclobenzaprine HCL 10 mg at HS PRN, Tizanidine HCL 4 mg. PRN
- Allergien
- Aspirin, Propranool HCL, Bactrim, Ketorolac, Zoloft, Sulfa, Latex, Toradol, Brand Spray, Milk, Coconut, Sulphasalazine, Zaleplon, Omeprazole, Flu vaccine, Plastic tape
- Vorherige Impfungen
- Flu vaccinations are listed in allergies for this patient -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dysgeusia
Pharyngeal paraesthesia
Throat irritation
Symptomtext
Pt c/o metallic taste and tingling/itchy throat 3 mins after vaccination. Given Benadryl 25mg @ 10:20. Pt stable and released from vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pharyngeal paraesthesia
- Hospital-Tage
- -
- Labordaten
- BP 164/101 HR 80 RR 16 96% RA @ 10:19 BP 145/102 HR 73 RR 16 95% O2 RA @10:22 BP 136/90 HR 75 RR 16 99% O2 RA @ 10:25
- Aktuelle Erkrankungen
- Unknown
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Not on file
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Arthralgia
Blood test
Burning sensation
Chills
Fatigue
Flushing
Mobility decreased
Musculoskeletal stiffness
Pain in extremity
Pyrexia
Sensory disturbance
Weight decreased
Symptomtext
I got the vaccine at 10 AM, at 5 AM I had a stiff neck. At 8 PM I had chills and fever. At 12 AM my upper body was throbbing, and my temperature was 99.6, it should be noted my temperature is 97.4. At 4 AM my wrists were burning. At 5 my shoulders, hips and knees were sore. At 8 AM the fever broke, and at 1 PM my left arm was still in pain. I have continued limiting movement in my shoulders. My shoulders, hips and knees. I have continuing flushes every 2-3 hours every night. My fever continues to go up to 99.8 and I have fatigue. I have also lost weight. On 11/17 I saw my doctor and they prescribed me prednisone. My symptoms are still continuing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mobility decreased
- Hospital-Tage
- -
- Labordaten
- Blood work
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Thyroid medication
- Allergien
- Codeine Iodine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Palpitations
Symptomtext
Client reported feeling dizzy and heart palpitations. Lasted for 15 minutes.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None reported
- Vorgeschichte
- Reports no chronic conditions
- Andere Medikamente
- First time taking probiotic, Rae. Otherwise, no other medications.
- Allergien
- Reports no allergies
- Vorherige Impfungen
- -
- Staat
- AZ
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 22.11.2021
- Impfdatum
- 17.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Blood test
Chills
Electrocardiogram
Palpitations
Supraventricular extrasystoles
Symptomtext
WOKE UP SHIVERING UNCONTROLLABLY, MY HEART WENT INTO SOME WEIRD RYTHM, CALLED AMBULANCE AROUND 8AM. TAKEN TO ER FOR THE DAY, TOLD I HAVE PACS TO GO ALONG WITH MY PVCS. GIVEN FLECAINIDE WHICH REALLY HASN'T DONE MUCH, STILL HAVING WEIRD PALPATIONS NEARLY A WEEK LATER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Palpitations
- Hospital-Tage
- -
- Labordaten
- ECGS, BLOOD TESTS,
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- IBS INTERSTITIAL CYSTITIS PVCS CHRONIC PANCREATITIS
- Andere Medikamente
- CLONIDINE, ATENOLOL,LISINOPRIL, GABAPENTIN, PROMETHAZINE
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 22.11.2021
- Impfdatum
- 19.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Condition aggravated
Fatigue
Interchange of vaccine products
Limb discomfort
Oedema peripheral
Pyrexia
Symptomtext
Moderna COVID?19 Vaccine EUA Vaccine received as booster; prior vaccination doses were BioNTech /Pfizer vaccine with second dose received 24 April 2021. Woke up feeling exhausted ~ 18 hours of booster dose. Slight fever noted ~ 1:00 PM (~ 101 deg). 3 x 81 mg chewable low dose aspirin taken. Pain started in left under arm area, same side as injection. Fever resolved by ~ 6:00 PM. Pain improved but remains under left arm and feels uncomfortable -- swelling under arm present on morning of 3rd day after receiving booster.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Condition aggravated
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Pepcid, as needed, but not taken morning of vaccination.
- Allergien
- Moxifloxacin
- Vorherige Impfungen
- Following initial COVID vaccination (Pfizer/BioNTech Lot ER8737( on 3 april 2021), fever (~100 - 101 deg) beginning ~ 5 days aft
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 17.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Hypoaesthesia
Pain in extremity
Paraesthesia
Symptomtext
This was a booster shot. Left foot pain, numbness and tingling at base of left leg, top of foot and wrapping around front of toes. Began around 36 hours after booster was given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Paraesthesia
- Hospital-Tage
- -
- Labordaten
- Exam by MD at a facility. No evidence of blood clot, no swelling. Monitor for swelling or increased pain.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Amerge for migraines
- Allergien
- Aspirin, cephalexin, imitrex
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 74,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Atrial fibrillation
Blood pressure decreased
Cardiac disorder
Diarrhoea
Hypotension
Laboratory test
Tachycardia
Vomiting
Symptomtext
Systemic: Abdominal Pain-Severe, Systemic: Cardiac Disorder (diagnosed by MD)-Severe, Systemic: Diarrhea-Severe, Systemic: Hypotension-Severe, Systemic: Tachycardia-Severe, Systemic: Vomiting-Medium, Additional Details: colostomy patient, explosive diarrhea started within 15 hours of vaccine, continued and turned to vomiting, primary md said use immodium, than then said go to hospital, at hospital was diagnoised with tachycardia/AFib, and blood pressure dropped very low. Hospital ran tests and could not find a cause other than combo of flu and covid vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Hypotension
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 07.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Extra dose administered
Headache
Pyrexia
Tremor
Symptomtext
Typical side effects including fever, chills, headache, etc. I also had a non typical response which included uncontrollable shaking of my hands and forearms. All of this subsided within a day or two.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Tremor
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Crohn's Disease has been in remission for many years. I have high calcium levels in my arteries and high cholesterol.
- Andere Medikamente
- No medications taken at the time of vaccination. I take cholesterol meds 5 mg Rosuvastatin every other day. I take baby aspirin nightly. I take Vitamin B, C, D3, E. I take Fish Oil, Co-Q-10, Vitamin K2, Lutein, Zeaxanthin
- Allergien
- Allergic to nickel and latex
- Vorherige Impfungen
- Typical side effects on first and second Moderna vaccine
- Staat
- CT
- Alter
- -
- Geschlecht
- M
- Eingang
- 15.11.2023
- Impfdatum
- 17.11.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Lethargy
Symptomtext
Patient had a sore shoulder and was lethargic for a couple of hours; Patient had a sore shoulder and was lethargic for a couple of hours; This spontaneous case was reported by a patient and describes the occurrence of LETHARGY (Patient had a sore shoulder and was lethargic for a couple of hours) and ARTHRALGIA (Patient had a sore shoulder and was lethargic for a couple of hours) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 prophylaxis. Previously administered products included for Product used for unknown indication: Pfizer (en6201, no expiration date was provided.) on 10-Feb-2021 and Pfizer. Past adverse reactions to the above products included Adverse drug reaction with Pfizer and Pfizer. On 17-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced LETHARGY (Patient had a sore shoulder and was lethargic for a couple of hours) and ARTHRALGIA (Patient had a sore shoulder and was lethargic for a couple of hours). At the time of the report, LETHARGY (Patient had a sore shoulder and was lethargic for a couple of hours) and ARTHRALGIA (Patient had a sore shoulder and was lethargic for a couple of hours) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication use information was not provided by reporter. The patient reported side effects to his one Moderna Covid-19 vaccine which was his third Covid-19 vaccine. The other vaccines including his fourth vaccine were all Pfizer vaccines. The patient received a Pfizer Covid -19 vaccine on the February 10, 2021, no expiration date was provided. Patient did not remember arm. Patient had a sore shoulder but did not have anything beyond that. Patient may had been lethargic for a couple of hours after the vaccine. The patient did drive himself home. The patient had the Pfizer Covid-19 for his first and second doses. The patient received first Moderna vaccine was November 17, 2021, expiration date was not known. Arm of injection was not known. Patient had a sore shoulder and was lethargic for a couple of hours. The patient thought that he had a Moderna vaccine for his fourth dose however at the end of the telephone interview the patient realized that he had a Pfizer vaccine for his fourth Covid-19 dose. Treatment medication use information was not provided by reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 51,0
- Geschlecht
- F
- Eingang
- 11.09.2023
- Impfdatum
- 11.09.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 51,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Amenorrhoea
Menopause
Musculoskeletal disorder
Pain in extremity
Symptomtext
No soreness or issue at first dose, no symptoms at all including no soreness at injection site, no swelling or bruising. 2nd dose resulted in extreme pain in arm for approximately 7 days with pain throughout arm to fingers. Unable to use left hand with confidence for this period. Patient was not yet in menopause confirming regular periods every 28 days for 3 to 4 days in length. No heat flashes, no symptoms of pre menopause. Following second dose patient did not menstruate again. Patient has not experience any pre or premeno symptoms and is now in menopause.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- Blood tests are available upon full scale health evaluation indication no medical issues cardiovascular or otherwise in October 2019. Again, in 2020 through health care. Dr. indicating optimal health, no concerns cardiovascular or otherwise.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None physical performed October 2019 indicated optimal, no negative health indication.
- Andere Medikamente
- Methylphenadate 10mg daily, Escitalopram 20mg daily.
- Allergien
- no allergies.
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 07.11.2022
- Impfdatum
- 06.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Mechanical urticaria
Pruritus
Rash papular
Skin irritation
Skin warm
Urticaria
Symptomtext
After getting my COVID-19 vaccine about 14 days later I started having hives and was itchy. It was so bad that that if you touched my skin it would leave a mark as if you could draw on me. Anything touching me would leave this raised rash on my skin as well. I reached out to my dermatologist and did a telehealth visit with them on November 22nd, 2021. They diagnosed me with Acute Urticaria and Dermographism. I was told to try a combination of ALLEGRA, ZYRTEC, and BENADRYL. I try to avoid BENADRYL and it did not work but I was given a prescription for triamcinolone acetonide cream. The cream made the rash manageable, but it did not resolve or eliminate the rash. The rash lasted for about 6 to 8 weeks but for that duration anything that contacted my skin would create that raised rash and irritation and if I scratched it created heat as well.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- Escitalopram; vitamin D3; probiotic; women's daily vitamin; vitamin B complex; VITA LF; magnesium bisglycinate
- Allergien
- Morphine; gluten sensitive; gabapentin; I V NEXIVA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 27.08.2022
- Impfdatum
- 22.12.2021
- Beginn
- 01.05.2022
- Tage bis Beginn
- 130,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Lymphadenopathy
Pain in extremity
Product administered at inappropriate site
Throat cancer
Symptomtext
severe limp nodes, swelling/had 3 lymph nodes, and an other that can't be seen; his arm got sore; HE THINKS THE SHOT WAS GIVING TO HIGH, AT THE PLACE OF INJECTION AND ALL AROUND AREA; on May2022 he got cancer in the throat.; This spontaneous case was reported by a patient and describes the occurrence of THROAT CANCER (on May2022 he got cancer in the throat.) in a 66-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch nos. 049L21A and 066F21A) for COVID-19 vaccination. The occurrence of additional non-serious events is detailed below. Concurrent medical conditions included Food allergy, Dairy intolerance, Food allergy and Food allergy. On 22-Dec-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 02-May-2022, received fourth dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) dosage was changed to 1 dosage form. In May 2022, the patient experienced THROAT CANCER (on May2022 he got cancer in the throat.) (seriousness criterion medically significant). On an unknown date, the patient experienced LYMPHADENOPATHY (severe limp nodes, swelling/had 3 lymph nodes, and an other that can't be seen), PAIN IN EXTREMITY (his arm got sore) and PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (HE THINKS THE SHOT WAS GIVING TO HIGH, AT THE PLACE OF INJECTION AND ALL AROUND AREA). At the time of the report, THROAT CANCER (on May2022 he got cancer in the throat.), LYMPHADENOPATHY (severe limp nodes, swelling/had 3 lymph nodes, and an other that can't be seen) and PAIN IN EXTREMITY (his arm got sore) had not resolved and PRODUCT ADMINISTERED AT INAPPROPRIATE SITE (HE THINKS THE SHOT WAS GIVING TO HIGH, AT THE PLACE OF INJECTION AND ALL AROUND AREA) outcome was unknown. No concomitant medication was reported. It was reported that symptoms had progressively worsened. Patient reported that lymph nodes were going to look cancerous and could be a false positive; they had not found any cancer cells in. No treatment medication was reported; it was mentioned that he was getting ready for chemotherapy and radiation. Company Comment: This spontaneous case reported by a patient concerns a 66-year-old male patient, with no relevant medical history, who experienced unexpected, serious (medically significant) event throat cancer, on the same month as vaccination with a fourth dose of mRNA-1273. He also reported severe lymph node swelling that were going to look cancerous but could be a false positive as cancer cells have not been found in them. Further clinical course of the throat cancer, diagnostic evaluation, and concomitant medications were not reported. No treatment reported; it was mentioned that he was getting ready for chemotherapy and radiation. The benefit risk relationship of mRNA-1273 is not affected by this report. This case was linked to MOD-2021-186718, MOD-2021-186664 (Patient Link).; Sender's Comments: This spontaneous case reported by a patient concerns a 66-year-old male patient, with no relevant medical history, who experienced unexpected, serious (medically significant) event throat cancer, on the same month as vaccination with a fourth dose of mRNA-1273. He also reported severe lymph node swelling that were going to look cancerous but could be a false positive as cancer cells have not been found in them. Further clinical course of the throat cancer, diagnostic evaluation, and concomitant medications were not reported. No treatment reported; it was mentioned that he was getting ready for chemotherapy and radiation. The benefit risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Dairy intolerance; Food allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 01.06.2022
- Impfdatum
- 16.11.2021
- Beginn
- 27.05.2022
- Tage bis Beginn
- 192,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Back pain
Nausea
Vomiting
Symptomtext
patient presented to hospital with nausea vomiting and back pain. treated with neausea medications and pain medication. Discharged home the following day.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Gerd, osteoarthritis
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 23.05.2022
- Impfdatum
- 19.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alopecia
Laboratory test abnormal
Pruritus
Symptomtext
I was very itchy and noticed my hair volume had decreased. I received treatment from a dermatologist; I was told my gluten levels were high.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- N/a
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- Migraines; GERD; Neuropathy; COPD
- Andere Medikamente
- Vitamin D Lexapro Wellbutrin Trazadone Loratadine Montelukast Breo Ellipta
- Allergien
- Penicillin; amoxicillin; PERCOCET
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 12.05.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.05.2022
- Tage bis Beginn
- 181,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
COVID-19
Ear pain
Fatigue
Lacrimation increased
Respiratory tract congestion
Rhinorrhoea
SARS-CoV-2 test positive
Sinus pain
Throat irritation
Vaccine breakthrough infection
Symptomtext
Breakthrough Case of COVID, So I started feeling a scratch in my throat, and then the next day my nose was running, my eyes were running, I was congested, my sinuses were hurting and my ears were hurting and I was very fatigued. Symptoms are starting to wear off, my chest is not as congested and the other symptoms are starting to wear down, also my joint hurt all over.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- COVID Test, PCR and Rapid.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Depression, ADHD, Ovarian Cyst.
- Andere Medikamente
- Multi-Vitamin, Junel Fe 1/20 (Birth Control)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 02.05.2022
- Impfdatum
- 11.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Dizziness
Symptomtext
CLT reported, not observed. CLT received Booster 1 on 11/11/2021 Moderna. Three hours after vaccination client experienced intermittent dizziness for three-four hours and then it was gone. Clt did not report it to Provider and did not seek any treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN
- Andere Medikamente
- -
- Allergien
- Kiwi, and animals
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 08.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Dizziness
Feeling abnormal
Headache
Rhinorrhoea
SARS-CoV-2 test negative
Sluggishness
Symptomtext
With first and second shot I got sick that lasted 2-3 days, I felt tired and ached all over and had a headache. On the third dose, I came home, the next day I felt brain foggy and felt sluggish. I had a headache, and I took Motrin, and it went away. So, what happened ever since then I have been foggy, almost like my brain is closed in, it is so hard to explain. And dizziness, it is not getting better, I said to myself I thought I had COVID-19, but I have never been sick. I had the sniffles, and it was from flowers in the house and tested for COVID-19 twice and they came back negative. I got all the shots within the recommended schedule. I saw my doctor and I had bloodwork that came back great, I even changed my diet thinking it was something I ate. But everything came back great no diabetes, cholesterol everything was good. My doctor sent me to an ENT and I have an appointment on 04/28/2022 to see if it is vertigo.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- Bloodwork - negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- GI issues
- Andere Medikamente
- Dicyclomine 20mg QHS, Vitamin E, D3; Low Dose Bayer Aspirin 81mg
- Allergien
- Iodine; Shellfish
- Vorherige Impfungen
- Influenza, I get tired and achy all over and I rest for 2-3 days, last flu shot was 2020. I have not taken it since I started th
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 17.04.2022
- Impfdatum
- 14.03.2021
- Beginn
- 22.03.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Alanine aminotransferase
Angiogram cerebral
Blood creatinine
Blood potassium
Blood sodium
Blood thyroid stimulating hormone
Computerised tomogram head
Full blood count
Glycosylated haemoglobin
Headache
Lipids
Magnetic resonance imaging head
Red blood cell sedimentation rate
Symptomtext
Continuous headache left side between temple and ear
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- See contiuation page 5/21/2021, CT HEAD WITHOUT CONTRAST, M.D., Sep 10, 2021, LANINE AMINOTRANSFERASE (ALT), M.D. Sep 10, 2021, LIPID PANEL, M.D. HEMOGLOBIN A1C, M.D. ERYTHROCYTE SEDIMENTATION RATE (ESR), M.D. THYROID STIMULATING HORMONE (TSH), M.D. CBC (COMPLETE BLOOD COUNT), M.D. SODIUM AND POTASSIUM, M.D. CREATININE, M.D. Oct 23, 2021, MRI BRAIN AND BRAINSTEM, M.D., Feb 3, 2022, MR ANGIOGRAM HEAD, M.D.,
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- OSTEOARTHRITIS OF RIGHT FIRST WRIST JOINT
- Andere Medikamente
- See contiuation page 800 mg ibuprophin, 1/day One a Day Mens 50+ Multivitamin, 1/day Airbourne Gummy, 1/day Triamcinolone Acetonide Inj 40 mg (KENALOG), 1/3 months
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 08.04.2022
- Impfdatum
- 11.11.2021
- Beginn
- 09.01.2022
- Tage bis Beginn
- 59,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Cough
Exposure to SARS-CoV-2
Fatigue
Headache
Oropharyngeal pain
Respiratory tract congestion
SARS-CoV-2 test positive
Symptomtext
01/09/2022: I started to have a sore throat and headache. My son contracted COVID from his preschool and so decided to test and the tests were coming back negative. On 01/12/2022 I tested positive for COVID. I stopped having a sore throat and fatigue around 10 days after. I still experience a bad cough and congestion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Rapid COVID test: 01/12/2022: Positive
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Fibromyalgia; Chronic Migraines; Asthma
- Andere Medikamente
- Levothyroxine 50mcg once daily, Wellbutrin 200mg once daily, Deplin 15mg once daily, Cymbalta 125mg once daily, Horizont 600mg three times daily, Trazadone 50mg once daily, Lunesta 2mg once daily, Gabapentin 600mg once daily, Emgality once
- Allergien
- Aspirin; Nature Throid
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 02.04.2022
- Impfdatum
- 20.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Dizziness
Fatigue
Headache
Symptomtext
fatigue; dizziness; chills; headache; This spontaneous case was reported by a consumer and describes the occurrence of FATIGUE (fatigue), DIZZINESS (dizziness), CHILLS (chills) and HEADACHE (headache) in a 52-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Pfizer vaccine (The patient received the Pfizer vaccine for her primary vaccination series). Past adverse reactions to the above products included No adverse event with Pfizer vaccine. On 20-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 20-Nov-2021, the patient experienced FATIGUE (fatigue), DIZZINESS (dizziness), CHILLS (chills) and HEADACHE (headache). At the time of the report, FATIGUE (fatigue), DIZZINESS (dizziness), CHILLS (chills) and HEADACHE (headache) had resolved. No concomitant drug details were reported. No treatment details were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 23.03.2022
- Impfdatum
- 10.11.2021
- Beginn
- 15.01.2022
- Tage bis Beginn
- 66,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Headache
Impaired work ability
Nasopharyngitis
Oropharyngeal pain
Rhinorrhoea
SARS-CoV-2 test negative
SARS-CoV-2 test positive
Symptomtext
01/15/2022 I started to have a little bit of a sore throat. On 01/16/2022 I decided to take a PCR test and tested negative for COVID. I felt like I had cold like symptoms. A runny nose, a headache. My symptoms were not too bad. I did take ibuprofen. I took another rapid test on 01/21/2022 and it was still positive. I went back to work on 01/26/2022. I did another rapid test on 01/27/2022 and it was negative.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Headache
- Hospital-Tage
- -
- Labordaten
- 01/16/2022: PCR Test: Negative; 01/21/2022: Rapid Test: Positive; 01/27/2022 Rapid Test: Negative
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High Blood pressure
- Andere Medikamente
- Lisinopril 5mg once daily; Biotin
- Allergien
- Acetophenone
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 19.03.2022
- Impfdatum
- 23.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Asthenia
Joint range of motion decreased
Motor dysfunction
Musculoskeletal stiffness
Pain
Pain in extremity
Swelling
Symptomtext
Pain, swelling, stiffness, decreased range of motion, progressive weakness, pain shooting down arm (sometimes into hand), decrease of motor control. Symptoms continue after four months and physical therapy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High cholesterol, low weight
- Andere Medikamente
- Claritin, omega 3, magnesium
- Allergien
- Shellfish, aspirin, naproxen, amoxicillin
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 59,0
- Geschlecht
- M
- Eingang
- 07.03.2022
- Impfdatum
- 02.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Asthenia
Back pain
Myalgia
Pain
Pain in extremity
Polymyalgia rheumatica
Rheumatoid factor increased
Symptomtext
After a week post vaccination, I started experiencing muscle pain in my neck and back. Then it slowly crept down to my biceps and triceps including the joints in my elbows. It got to the point where I was getting pain in my thighs and calves. Around the 26th of December, the pain had progressed to all over the body. It was debilitating. I was then being diagnosed with polymyalgia rheumatica and was prescribed hydrocodone and 10mg of prednisone. By the next day muscle pain was gone and joint pain was gone. Since then I have been treated with prednisone, and am now adjusting medications to keep it under the control. Symptoms are still there if I do not get treatment and take prednisone.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- Blood test verified diagnosis of polymyalgia rheumatica Level on blood was 80 which has a baseline of 0-12. After prednisone my levels went back down.
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Hypertension
- Andere Medikamente
- Ramipril 10mg daily
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 72,0
- Geschlecht
- F
- Eingang
- 22.02.2022
- Impfdatum
- 16.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood pressure decreased
Rash
Symptomtext
BLOOD PRESSURE DROPPED FULL BODY RASH
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- ONE A DAY VITAMIN TUMERIC FISH OIL CALCIUM VITAMIN D
- Allergien
- SULFU NITROFULANTERNON VACCINES SHELL FISH ALLERGY BEE STING
- Vorherige Impfungen
- SHINGLES VACCINE RASH
- Staat
- OH
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 05.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood thyroid stimulating hormone
Chronic spontaneous urticaria
Dyspepsia
Full blood count normal
Metabolic function test
Pruritus
Sleep disorder
Urticaria
Symptomtext
2 weeks following the 3rd Moderna I developed some pruritis. That night I woke up with severe heart burn and hives throughout my body. I was seen at an urgent care and started taking 20 mg of pepcid twice daily, 20 mg of zyrtec twice daily and benadryl for breakthrough. I also took Omeprazole for 1 week. The heartburn resolved, but the hives continued and did not resolve. I had tried different antihistamines. Eventually I was seen by an allergist who diagnosed me with chronic spontaneous urticaria. Currently I am taking zyrtec 20 mg twice daily, pepcid 20 mg twice daily, and singulair 10 mg. the hives have persisted.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chronic spontaneous urticaria
- Hospital-Tage
- -
- Labordaten
- CBC, CMP, TSH - all normal
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- No
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 16.02.2022
- Impfdatum
- 07.12.2021
- Beginn
- 18.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Antinuclear antibody negative
Blood cholesterol increased
Chlamydia test
Full blood count
HIV test negative
Hepatitis B surface antigen negative
Laboratory test normal
Low density lipoprotein increased
Metabolic function test normal
Neisseria test negative
Treponema test negative
Urticaria
Symptomtext
11 days after 3rd Moderna shot I broke out in hives, that are ongoing despite famotidine and montelukast. Was supposed to take Allegra also, but has not picked it up.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- Lab corp. done 1/4/22 Has hi LDL and cholesterol 246 on 1/4/22, CBC, CMP neg, chlamydia, Neisseria gonorrhoeae. Neg, ANA neg RPR neg, HIV neg, Foods neg HbsAg neg. No thyroid tests done because patient seemed to be improving.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- None
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 15.02.2022
- Impfdatum
- 01.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Ammonia normal
Chills
Influenza
Influenza virus test positive
Pyrexia
SARS-CoV-2 test negative
Symptomtext
24 hours after booster I started having a real high fever and chills. After 3 days it didn't go away and my temperature was 104 so I went to the hospital and discovered that I had the flu. I'm not sure if this was coming on at the time of the booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- I was tested at the hospital for the flu, Covid and ammonia. Discovered that I had the flu.
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- I have flu symptoms regularly after vaccines, but not this bad or for how long.
- Staat
- CO
- Alter
- 26,0
- Geschlecht
- M
- Eingang
- 14.02.2022
- Impfdatum
- 16.01.2022
- Beginn
- 26.01.2022
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Urticaria
Symptomtext
Systemic: Allergic: Rash Generalized-Medium, Systemic: Full Body Hives-Medium, Additional Details: Patient reported onset of full body hives about 10 days after booster dose of Moderna covid vaccination. Patient reports consulting with physician to confirm delayed onset allergy. Patient has been taking famotidine, benadryl, cetirizine, and steroid to treat hives. As of date of this report, patient is still experiencing hives, with slow recovery after antihistamine and steroid treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 08.02.2022
- Impfdatum
- 29.12.2021
- Beginn
- 29.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Asthenia
Fatigue
Feeling cold
Headache
Hot flush
Impaired driving ability
Loss of personal independence in daily activities
Symptomtext
1st Dosage: Same day, received headaches, tiredness, fatigue, weakness whole body, coldness in body, hot flashes. Next morning-have slept for around 12 hours. Following few days: Same symptoms for the first 4 days, the 5th day finally feeling better Did not take any other medications over the counter or prescriptive medications. Naturally recovered from sickness side effects of the medications. 2nd Dosage: Same as above. 3rd Dosage: 1st Day immediately, fatigue, tired, weakness. 2nd Day: could not drive at all. 3rd Day: could not drive at all. Did not drive for 5 days from 12/29/2021 Booster Shot Moderna Vaccine Terrible feeling of fatgiue, tiredness, weakness and coldness at times. Muscular function could not allow me to do daily activities such as basic local driving or even any type of driving at all. I was basically bedridden every time I had these vaccines. I hope your future Covid-19 vaccines, especially Moderna will improve with time without adverse side effects at all.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- Unknown.
- Aktuelle Erkrankungen
- No.
- Vorgeschichte
- No.
- Andere Medikamente
- No.
- Allergien
- Xiidra Dro 5% Prescription Eye Drops Latex Material: gloves Unnatural and natural foods allergic reaction to: 1) Any hints of artificial coloring 2) Cooking spices: pepper in salt and pepper; black pepper, paprika, cayenne 3) Herbal spices: Dill 4) Hot spices: in certain food; jalapeno peppers, chili, wasabi, capsaicin and allyl isothiocyanate 5) Any chemical based food products that are laboratory made foods such as PLANT BASED foods
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 25,0
- Geschlecht
- M
- Eingang
- 04.02.2022
- Impfdatum
- 02.12.2021
- Beginn
- 13.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dyspepsia
Mechanical urticaria
Pruritus
Urticaria
Symptomtext
Hives and heartburn. The first few days were most severe. Taking prednisone 20mg eliminated symptoms until stopped taking after 5 days. Heartburn and hives returned. Heartburn went away in a few days thereafter. Hives turned into dermatographia and itchiness, which has lasted since. Antihistamines reduce itchiness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- IBS-D, Asthma
- Andere Medikamente
- Flonase
- Allergien
- Peanut, Zithromax, seasonal allergies
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 06.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 6,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Malaise
Pain in extremity
Symptomtext
Malaise, joint aches, sore arm x 30 hour
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- Azo-Sulfisoxazole, Demerol, Flexeril, Morphine, Pcn, Vicodin
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 21.01.2022
- Impfdatum
- 13.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Injection site nodule
Symptomtext
Patient had a small knot at site of injection. Size of pinky fingernail. There was no pain or bleeding. Applied cold compress to injection site and monitored the site for 30 minutes. Instructed patient to continue with cold compress for next 48 hours. If the site became larger or worse with redness/fever told patient to seek medical attention. Patient notified us 1-21-22 that she had issues with site and she did see a Dr for treatment.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site nodule
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Discomfort
Ear discomfort
Erythema
Pruritus
Rash
Urticaria
Symptomtext
9 days after my Moderna booster I got itchy on my hands and feet. It got worse to full blown hives and a rash. I went to urgent care and got on a steroid. The hives got better but not gone after the steroid. Approx Day 2 after steroid hives came back. Very uncomfortable . I also had burning and really red ears. Saw a doctor and allergist and am currently on Zyrtec and Allegra.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Zoloft 50 mg Fish oil Probiotic Cranberry Digestive enzyme Adrenal support Vitamin D and K Two a day multi vitamin Curcumin Iron
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 18.01.2022
- Impfdatum
- 24.11.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Rash
Urticaria
Symptomtext
Urticaria and rash x 6+ weeks. Treated with Hydroxyzine, Pepcid, and Triamcinolone cream.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Hypertension.
- Andere Medikamente
- Ramipril 5mg daily.
- Allergien
- None.
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 20.11.2021
- Beginn
- 29.11.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
chronic hives
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Hashimotos
- Andere Medikamente
- Levothyroxine
- Allergien
- -
- Vorherige Impfungen
- Moderna - covid arm
- Staat
- CA
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 16.01.2022
- Impfdatum
- 23.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Burning sensation
Rash
Urticaria
Symptomtext
Severe chronic uticaria, wheals, non stop burning, rashes, welts. Severe for 14 days, and is now ongoing and intermittent
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Rash
- Hospital-Tage
- -
- Labordaten
- Urgent care visit. 12/3/21
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Severe chronic disabling spine condition
- Andere Medikamente
- Oxycontin, oxycodone, carisoprodol, rosuvastatin, docusate sodium, Calcium complex, fish oil, b-complex, vit-d, tumeric, astaxanthin, vit-c, b-12, dry mushrooms complex. Acacia fiber, collagen protein.
- Allergien
- Certain NSAIDS. Some processed nuts.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 03.01.2022
- Impfdatum
- 08.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Back pain
Chills
Headache
Nausea
Neck pain
Pain
Pain in extremity
Pyrexia
Symptomtext
She got her vaccine, had severe backaches, her legs were aching and there was not a part of her that did not hurt. She felt nauseous, her neck hurt, her head hurt. She had fever and chills. They lasted for about 24 hours and they left. She did not take anything for her symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Back pain
- Hospital-Tage
- -
- Labordaten
- None.
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- Thyroid disease, lung scarring (bronchiectasis), three lobectomy of thyroid.
- Andere Medikamente
- Synthroid, Estradiol, Vitamin D3, Vitamin C, fish oil, multivitamin.
- Allergien
- Multiple antibiotic allergies (testing this month). Latex, adhesive tape.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Allergy test negative
Blood immunoglobulin M increased
C-reactive protein normal
Full blood count normal
Mechanical urticaria
Pruritus
Rash
Thyroid function test normal
Urticaria
Symptomtext
Severe itchy hives and rashes, dermatographia
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- CBC, Thyroid panel, CRP, food allergies panel - all normal IGMs came back high
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 31.12.2021
- Impfdatum
- 05.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Laboratory test
Neck pain
Pain in extremity
Sensory disturbance
Symptomtext
patient reports neck pain, legs pain, sensory abnormalities starting about 2 weeks after her latest coronavirus booster. She states she cannot think of any other factor or change to attribute to - prior to developing these symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Neck pain
- Hospital-Tage
- -
- Labordaten
- Labs and further evaluation performed in the ER
- Aktuelle Erkrankungen
- liver disease hypertension heart disease
- Vorgeschichte
- liver disease hypertension heart disease history of silicone toxicity antiphospholipid abnormality
- Andere Medikamente
- aspirin pepcid losartan metoprolol pravastatin sucralfate
- Allergien
- contrast media
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 27.12.2021
- Impfdatum
- 24.11.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 16,0
- Dosis
- UNK
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Pruritus
Urticaria
Symptomtext
Itchy palms and foot soles in the morning (for about 15 minutes). After a few days added: - intense itching/burning sensation on hands, wrists, feet (upper surface), sometimes on scalp, torso and thighs, lasting for about 15 minutes a few times a day (not occurred during the sleep) - itching and hives in the same areas for 5-30 minutes when walking outdoors or being nervous. Doctor prescribed Benadryl 25mg 2 times a day for 4 days to see if it stops the condition. It alleviated the symptoms when taken, except for morning itchy palms and foot soles. Progress TBD after stopping the medicine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Irritable bowel syndrome, eczema (or eczema-like dermatitis)
- Andere Medikamente
- Centrum Women multivitamins, Vit. D 400 UI
- Allergien
- Seasonal pollen allergy during springtime until moving 7 years ago, no allergy at present time
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 25.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Mechanical urticaria
Pruritus
Urticaria
Symptomtext
Hives and dermatographia started 9 days after Modern booster. I have been taking 2 types of antihistamines to control the hives and itch. If I skip a dose, the hives immediately appear. It has been 10 days and the hives are still appearing.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Hair and nail vitamins
- Allergien
- Ibuprofen, shellfish
- Vorherige Impfungen
- -
- Staat
- TN
- Alter
- 56,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 17.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pruritus
Rash
Urticaria
Symptomtext
Itchy hives (rash) over entire body; took Benadryl and received steroid shot by healthcare provider. Itching resolved, then returned.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- None.
- Andere Medikamente
- Regular daily medications.
- Allergien
- Penicillin.
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 28,0
- Geschlecht
- M
- Eingang
- 23.12.2021
- Impfdatum
- 16.11.2021
- Beginn
- 27.11.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Blood test normal
Mechanical urticaria
Symptomtext
11 days after I got my Moderna shot, I started having severe dermatographism after having a seafood dinner. Went to urgent care to get this checked out, and the recommended me to go see an allergist. I conducted a blood test through an allergist (because I cannot do a skin prick test) and I am not allergic to shellfish based on the results. I saw online other patients who received the vaccine booster and also have dermatographism - so I feel suspicious this is strongly related. After seeing my allergist, I am taking Zyrtec daily, and it has helped reduce the symptoms, but I still continue to have dermatographism when the medicine effect wears off.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None.
- Vorgeschichte
- -
- Andere Medikamente
- None
- Allergien
- None known.
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 22.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Erythema
Interchange of vaccine products
Pruritus
Symptomtext
Pfizer primary series; Moderna Booster Itchiness and Redness. PT reports no shortness of breath or throat swelling. No difficulty breathing noticed. Respirations equal and full. Redness noted on PTs back and itchiness throughout torso. PT did not mention to clinical and non clinical staff that she had a reaction in the past. PT reports the same reaction after the second covid vaccine. PT failed to mention any health issues/allergies to clinical reviewer or vaccinating nurse. Clinical Manager notified immediately and facility physician notified by facility staff. MD present in the room at 1005 11/30/21. Pt given Benadryl 50mg PO @09:55. Pt stable and released from the vaccination site. Recommended f/u w/ PCP and avoid mRNA vaccines in the future.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- Pfizer Covid vaccine, otherwise unknown to this writer.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 89,0
- Geschlecht
- F
- Eingang
- 19.12.2021
- Impfdatum
- 13.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site rash
Insomnia
Pruritus
Symptomtext
After developing a bright red rash at the injection site(upper left arm) a week after receiving the booster shot, the rash got better, but I started itching at constantly changing spots on my body. I still have these terrible ,itches (without outward signs) which are preventing me from sleep and are terrible during the day. This is now 5 weeks after the vaccination, and
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- Have Marfan?s syndrome
- Andere Medikamente
- Pantroprazole 40 mg, eye drops: Dorzolamide HCI/Timolol, Ketoralac, Nortriptyline Hydro 20 md, Hydrochloride Nortriptalyne 20 mg , Paroxitine 20 mg
- Allergien
- Tree nuts, milk (lactose intolerant)
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 18.12.2021
- Impfdatum
- 17.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
Hives onset 1 week later.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 30.11.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Mechanical urticaria
Pruritus
Urticaria
Symptomtext
On the 30th I started getting a full body itching, My scalp legs and feet and my whole body. that lasted a week and I went to see the dermatologist about a week a go and she diagnosed me with Dermatographism and Hives. Now my skin it'll leave red marks like I scratch my skin. She said this is potentially from the vaccination. The itching went but the red patches is still there. She also gave me Zyrtec until the problem resolve so I'm still taking it.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Mechanical urticaria
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 20.11.2021
- Beginn
- 01.12.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Flushing
Pruritus
Urticaria
Symptomtext
Hives (urticaria) randomly appearing all over body, sometimes spontaneously but sometimes in reaction to skin pressure. Hives seem to recur mostly in the morning, in the evening, and in the middle of the night. Hives mostly appear on legs, trunk, armpits, neck, scalp. Other symptoms include itchy palms and flushing in and around the ears. Managing symptoms successfully with Benadryl or 24-hr Zyrtec, usually taken before bed, and hydrocortisone cream.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Mirena intrauterine device, topical tacrolimus ointment for perioral dermatitis
- Allergien
- stannous fluoride
- Vorherige Impfungen
- fatigue and swollen lymph nodes from flu vaccines (annually), flu-like symptoms from second Moderna vaccine on 04/07/2021 at age
- Staat
- -
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 05.12.2021
- Beginn
- 05.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Interchange of vaccine products
Symptomtext
Pt received Janssen Primary series and Moderna Booster 2mins post vaccination pt reported dizziness Vitals: 137/88, 76, 16 Placed in a recovery position, VSS Pt stable and released from the vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: hx gall bladder removal, DM2, HTN, HLD, Hypothyroidism
- Andere Medikamente
- Medications: Acarbose 100mg PO daily Bupropion 75mg PO daily ergocalciferol 50000 units PO Qweek fenofibrate 48mg daily glimepiride 4mg PO Daily Levothyroxine 50mcg PO daily Lisinopril 20mg PO daily Simvastatin 20mg PO QHS
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- F
- Eingang
- 16.12.2021
- Impfdatum
- 06.12.2021
- Beginn
- 06.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Anxiety
Dizziness
Symptomtext
25mins post vaccination pt reported dizziness and anxiety. Vitals: 147/80, 71, 20, 100% -- > 155/79, 57 Pt stable and released from the vaccination site. Recommended f/u w/ PCP if sx continue tomorrow
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: Varicose veins of both lower extremities with complications Increased BMI Hypothyroidism Radial styloid tenosynovitis (de quervain) Carpal tunnel syndrome Anxiety Anemia
- Andere Medikamente
- Medications: Ibuprofen 600mg daily
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 13.12.2021
- Impfdatum
- 08.11.2021
- Beginn
- 25.11.2021
- Tage bis Beginn
- 17,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Symptomtext
I have chronic joint pain and my hips hurt constantly. I never had any hip joint pain prior to vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- N?A
- Aktuelle Erkrankungen
- N/a
- Vorgeschichte
- N/A
- Andere Medikamente
- Klonopin
- Allergien
- Penicillin, prednisone, Flu Shot
- Vorherige Impfungen
- Flu Vaccine
- Staat
- IN
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 10.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- 09.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Injection site nodule
Injection site warmth
Neck pain
Nodule
Spinal pain
Symptomtext
Large knot and soreness in armpit, soreness in neck and upper spine. Knot at injection site, very warm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Tylenol rapid release
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 09.12.2021
- Impfdatum
- 17.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Abdominal pain
Rash
Urticaria
Symptomtext
I experienced hives, rash and abdominal pain.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- High blood pressure
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 76,0
- Geschlecht
- F
- Eingang
- 09.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Insomnia
Pruritus
Skin warm
Urticaria
Symptomtext
Patient's husband reports hives, warm skin, insomnia, itching - called PCP dr who prescribed OTC benadryl. Reports symptoms persist and getting worse as of today 12/9/2021. Advised to physically see a provider either PCP or urgent care for further evaluation and diagnostics.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None reported
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Coronary Artery Disease
- Andere Medikamente
- 4 medications (including blood thinners)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Asthenia
Blood pressure increased
Computerised tomogram head
Dizziness
Electrocardiogram
Headache
Hypertensive urgency
Laboratory test
Symptomtext
dizzy, weak and having headache, elevated blood pressures - hypertensive urgency/emergency - required urgent care and then ER evaluation.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- ECG, full lab panel, CT scan of the head
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hyperlipidemia
- Andere Medikamente
- losartan, simvastatin
- Allergien
- sulfa abx - hives
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 06.12.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: ja
Erholt: nein
Adverse reaction
Discomfort
Feeling hot
Immediate post-injection reaction
Pain
Pain in extremity
Peripheral swelling
Sleep disorder
Symptomtext
Left arm immediately felt a sharp hot pain traveling down arm; within hours arm began to swell, throb; Tylenol was taken for discomfort. During night pain kept patient awake and was unable to find a comfortable position for arm. Next day information was sought for adverse reaction ad was told symptoms were ?normal? . Within 48 hours patient had to be rushed to ER for adverse reaction to vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- Tests were done on: 11/21/2021 Regular doctor was seen on: 11/22/2021 Rex?s were prescribed but patient has no income and could not afford treatment = home care is all patient can do at this point
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- HBP
- Andere Medikamente
- High blood pressure meds: lisinopril; hydrochlorothiazide Allergies:: Loratadine Multivitamins otc
- Allergien
- Oral antibiotics, cholesterol meds = deadly reaction
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- F
- Eingang
- 05.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Feeling abnormal
Feeling hot
Injection site erythema
Injection site induration
Injection site pruritus
Injection site swelling
Injection site warmth
Pallor
Peripheral nerve injury
Sensory disturbance
Vaccination site reaction
Symptomtext
In the first 15 minutes after the vaccination, I experienced reduced nerve sensation in the arm of the vaccination site. Following, I experienced short term heat in my ears. At 17 minutes or so, my right arm nerves became amplified. The sensations passed and I continued on with my day. At some point, I noticed itching at the injection site. At 7:30 pm I arrived home from work and experienced chills. I took a hot bath for hours as hot as I could make it I was woosy and pale. After tylenol and food I went to bed. Friday morning, my arm was hot, hard, and swollen at the injection site. At nearly 10 pm 12/4 the red circle around injection site (2.5 inches in diameter or so) is still present
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- significant sinus congestion (sinusitis) and lethargy Sunday November 28th
- Vorgeschichte
- mold allergies panic disorder nerve discomfort in upper back
- Andere Medikamente
- Prozac 25 mg Rainbow Light Prenatal One Multivitamin SSS Tonic 3 Tablespoons Fluticasone Propionate nasal spray (50 mcg) Azelastine HCl nasal spray (137 mcg)
- Allergien
- Zpak
- Vorherige Impfungen
- Moderna 80777-273-99, 32, feeling unwell day after shot missed work- no injection site reaction
- Staat
- CA
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 04.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Oral herpes
Pyrexia
Symptomtext
Fever of 102.4, treated with Acetaminophen resolved after 18 hours. Development of cold sore on Dec 4, 7am, treated with acyclovir.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pyrexia
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- allergy induced asthma, probable Marfans syndrome
- Andere Medikamente
- none
- Allergien
- penicillin tree nut allergies
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 46,0
- Geschlecht
- F
- Eingang
- 04.12.2021
- Impfdatum
- 12.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 12,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Pruritus
Rash
Rhinorrhoea
Urticaria
Symptomtext
Nov 12 booster Moderna #3 Nov 20-27 was in SoCal for Thanksgiving Nov 22 started to get runny nose, took Claritin at night and the next day was fine Nov 25-26 noticed itchiness on the tops of the feet, resolved Nov 27 drove back, that night had itchy scalp Nov 28 experienced full body itching (not on face, palms, bottom of fee)t. Itchiness would start. Hives (urticaria) rash throughout my body. Notably on arms, legs, back, neck, scalp, behind ears, etc. The rash would last 30 - 60 min and resolve, and then appear at a different body part. Nov 29, 30 took 2 cap of benadryl to sleep, which helped Dec 1 stopped medication, itchiness started again. Dec 2 - prescribed cetirizine (ZYRTEC) 10mg Tab; hydrOXYzine HCl (ATARAX) 25mg Tab, REFERRAL TO ALLERGY, INT
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- None performed. Video visit with a nurse practitioner occurred on December 2nd.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None / Recovering from a hamstring pull/tear from June 2021
- Andere Medikamente
- Vitafusion Women's Multi daily vitamin, Vitafusion Calcium 500 mg
- Allergien
- Gentamycin Olive tree extract Dust mites
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 13.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 11,0
- Dosis
- 3
- Route/Site
- SC / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Sensitive skin
Skin discomfort
Urticaria
Symptomtext
This was my booster shot for Moderna. I did not experience the following symptoms for my first two doses. I began itching on my stomach the evening reported. This itching progressed and became intense on the palms of my hands and my feet for the next several days. On 11/28/21 I noticed that when I itched my torso or neck, white/red welts/hives appeared where I itched. This has continued. The itching on my hands and feet as gotten better but has not completely gone away. I have not changed anything, to my knowledge that would have brought on this type of reaction; no change in diet, clothes, detergents, etc. I have also found that my skin feel sensitive to clothing that I have previous worn and has never caused me discomfort. Hot showers also irritate my skin and aggravate the itching.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- Have not gotten care as it seems to maybe be getting better. However, if it gets worse or not 100% I will likely seek medical care.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 72,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 23.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Erythema
Fatigue
Headache
Hypersensitivity
Malaise
Pain
Urticaria
Symptomtext
Patient reported waking on 11/24/2021 approximately 0800 with severe fatigue/malaise, headache, body aches. Pt spouse later entered and stated pt appeared to be having allergic reaction. Pt spouse noticed welps on skin and generalized redness across face and chest. Pt took Benadryl 50mg PO and symptoms resolved. Pt states that on 11/25/2021, he felt better with minimal fatigue remaining.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- hypertension, hypercholesterolemia, hypothyroidism
- Andere Medikamente
- bumex, aspirin, synthroid, cymbalta, lipitor, atenolol,
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 02.12.2021
- Impfdatum
- 30.11.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Ageusia
Chills
Decreased appetite
Pyrexia
Rash
Rash macular
SARS-CoV-2 test negative
Symptomtext
Spotted Rash developed over whole body when receiving booster dose of Moderna. Lot: 066F21A; Exp: 02/03/2022 Administered 11/30 at 1200; 10-12 hours later: fever, chills, loss appetite, loss taste; 36 hours later: fever persists, loss appetite, spotted rash across chest/legs now present. At home COVID test taking 12/1 and is negative. 1st DOSE Moderna: 12/31/20; 2nd DOSE Moderna: 1/28/21.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- At home covid test negative
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 01.12.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Interchange of vaccine products
Symptomtext
Pt previously received Janssen COVID vaccine 5mins post vaccination pt reported dizziness. Vitals: 119/74, 82, 18 Pt stable and released from the vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: CHRONIC LOW BACK PAIN 05/14/2021 CERVICAL HIGH RISK HPV TEST POSITIVE 02/05/2021 GENERALIZED ANXIETY DISORDER 11/15/2017 FHX OF BREAST CANCER 08/29/2013 FHX OF DM 07/13/2012 MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE 10/19/2011
- Andere Medikamente
- Medications: Apri 0.15-0.03mg tab PO daily Venlafaxine 75mg PO daily
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 25.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 9,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lip swelling
Pain in extremity
Tendonitis
Urticaria
Symptomtext
Hives for several days over abdomen, back, arms, hands and feet. Tendon swelling and pain in hands and feet, and marked lip swelling.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 22,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Pain in extremity
Symptomtext
pt came in today claiming her arm that got the moderna vaccine is still sore/painful about 3 on pain scale and pt asked if that is normal. Told the patient people do not usually have pain for that long and to see her doctor as soon as she can. She said she has an appointment on 12/2/21 and she is not too worried. pt has some pain on her arm that got the moderna vaccine and the pt is going to see the doctor on 12/2/21 and she was not concerned just asking for our advice on what to do.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Urticaria
Symptomtext
10 days after Moderna booster, I developed widespread hives over my head, neck and torso. The hives and hyper-reactivity of my skin have persisted now through at least 19 days after my booster (today, 11/24) despite a Prednisone taper and daily Zyrtec.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Urticaria
- Hospital-Tage
- -
- Labordaten
- Not at this time. I have an appointment with an allergist on 12/6/21.
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Prenatal vitamin, Vit D supplement
- Allergien
- Codeine, penicillin, sulfa
- Vorherige Impfungen
- Delayed localized hive (10 days post vaccine) at injection site for initial Moderna Covid vaccine. Lasted ~1 hour.
- Staat
- NE
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 23.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Chills
Headache
Vomiting
Symptomtext
Chills, headache, vomiting for 24 hours after booster shot.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 23.11.2021
- Impfdatum
- 22.11.2021
- Beginn
- 22.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysgeusia
Fatigue
Injection site pain
Nausea
Pain in extremity
Symptomtext
Metallic taste in mouth, mild fatigue, mild nausea, injection site tenderness, sore left arm.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Fatigue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Anxiety
- Andere Medikamente
- Sertraline
- Allergien
- Penicillin
- Vorherige Impfungen
- Sore arm
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 22.11.2021
- Impfdatum
- 14.11.2021
- Beginn
- 14.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Dizziness
Flushing
Hyperhidrosis
Symptomtext
10mins post vaccination pt c/o flushing/sweating and dizziness Vitals: 09:38 132/72, 103, 20, 100% -- > 09:50 134/81, 106, 18, 100% 09:55 Pt is standing and states that she is feeling better. Symptoms resolved.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Recent referral to Uro for blood in the urine
- Vorgeschichte
- PMH: Crohn's, Persistent blood in the urine
- Andere Medikamente
- Medications: cyanocobalamin PO Daily additional medications unknown
- Allergien
- Allergies: Cephalexin, Ciprofloxacin (leg numbness), Ciprocinonide (Rash, Numbness)
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 36,0
- Geschlecht
- F
- Eingang
- 22.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 10,0
- Dosis
- 3
- Route/Site
- - / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: ja
Blood iron decreased
Blood test abnormal
Diarrhoea
Fatigue
Peripheral swelling
Vomiting
Symptomtext
Prior to the adverse event. Patient experienced Diaherrea, Fatigue, and Vomitting. Period, lasted 2 days longer than normal. Prior to the Vaccine, Patient experienced swelling, on both legs from the 2nd dose. It was ruled out that it was not a Bloof Cot
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Diarrhoea
- Hospital-Tage
- -
- Labordaten
- Blood Test (Monday, November 15th, 2021) Iron Levels were incredible low
- Aktuelle Erkrankungen
- On Period
- Vorgeschichte
- Asthma
- Andere Medikamente
- Abuterol, Vitamin D, 6 mg Melatonin, Senna Cot, Colace, Flovent
- Allergien
- Pollen
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 35,0
- Geschlecht
- F
- Eingang
- 20.11.2021
- Impfdatum
- 18.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Injection site erythema
Injection site pain
Injection site pruritus
Injection site warmth
Pain
Pyrexia
Urticaria
Symptomtext
November 19th at 10:00 a.m. whole body aches, chills, fever of 100.1, substantial pain as injection site. 11:00 p.m. 2 inch red, welt, hot November 20th 9:00 a.m. Welt had increased by a quarter of an inch. Still very red & hot November 20th 8:00 p.m. whilst head increased by an additional quarter of an inch. Still red and hot and now itchy
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Migraines
- Andere Medikamente
- 300 mg of Wellbutrin, vegan vanilla Shakeology, biotics research bioprotect
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 13.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Injection site infection
No adverse event
Symptomtext
60 year old male client arrives to vaccination site requesting 2nd dose in Moderna series. Client reports that approximately 1 week after receiving his 1st dose of Moderna vaccine, that he experienced a localized infection at the injection site on his right arm. Client reports seeing Primary Care Provider who provided treatment of antibiotics for a few days. Client reports that infection resolved after completion of antibiotics. Elevated issue to Clinical Supervisor, who received approval from Dr. to proceed with administration of 2nd dose in Moderna series, with administration in left arm. Second Moderna dose was administered by RN on 11/13/21 at approximately 11:00 AM. Lot # 066F21A. Explained emergency precautions to client who verbalized understanding. No adverse symptoms reported during observation period.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site infection
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 18.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 16.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Pain in extremity
Symptomtext
Swelling and soreness in armpit
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain in extremity
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- No
- Vorgeschichte
- No
- Andere Medikamente
- Lisinopril 10 MG-Hydrochlorothiazide 12.5mg
- Allergien
- No
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 7,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dizziness
Electrocardiogram
Vertigo
Vitamin B12
Symptomtext
Onset of dizziness/vertigo. At approximately 8 days after booster vaccination, dizziness persisted through the entire day. 13 days later, dizziness is still intermittently reoccurring.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dizziness
- Hospital-Tage
- -
- Labordaten
- EKG, Blood pressure, B12 blood test.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 40,0
- Geschlecht
- F
- Eingang
- 16.11.2021
- Impfdatum
- 14.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- UNK
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Abdominal pain
Back pain
Discomfort
Groin pain
Sleep disorder
Symptomtext
I woke up almost 12 hours from the time I received the booster shot. I had extreme pain in my right abdomen/groin as well as the right lower side of my back. Pain so bad that it reminded me of child birth labor. I could not get comfortable standing, walking, lying down. I took 2 ibuprofen and it did do anything. Finally at 7:30-8am it settled down so I could sleep. I woke up again at 10:30 with the horrible pain again. It last another hour or so and then stopped. I have had kidney stones before. So possibility it was that and just a coincidence. However, I have never felt that bad from a kidney stone before. It has now been 36 hours since it stopped and I have not seen a passed stone in the toilet. I only called my Drs office but never went in as the pain stopped. Too much longer and they told me to just go to the ER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Abdominal pain
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- No illnesses.
- Vorgeschichte
- None
- Andere Medikamente
- 40mg Fluoxotine, 150mg generic Wellbutrin XL, Vitamin D, Iron, Magnesium
- Allergien
- Potential allergy to Penicillin when I was a kid.
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 31,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Fatigue
Pain
Pyrexia
Symptomtext
I woke up in the morning with a fever. The fever was 100.4. I felt very achy. My joints really hurt, and I was tired. I stayed in bed most of the day and by 5pm I was feeling better.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- Norlyda Vitamin D Postnatal Vitamin
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 50,0
- Geschlecht
- F
- Eingang
- 15.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site erythema
Injection site swelling
Type IV hypersensitivity reaction
Symptomtext
3 days after injections left upper arm erythema and swelling without clear demarcation and no systemic signs of infections diagnosed as delayed hypersensitivity reaction. Prescribed oral antihistamine, acetaminophen, topical steroid, icing to area.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- diabetes type 2, asthma hypertension, hyperlipidemia, migraines
- Andere Medikamente
- acetaminophen
- Allergien
- penicillin
- Vorherige Impfungen
- -
- Staat
- VA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Arthralgia
Chills
Fatigue
Headache
Joint range of motion decreased
Muscular weakness
Musculoskeletal stiffness
Nausea
Pyrexia
Vomiting
Symptomtext
(approximately same for shot 2 and 3...1st vacc produced only a slightly red lump at injection site) For #2 injection Chills started 9 hours post vaccine. Fever of 103.3 degrees F began shortly thereafter and remained at that temp for 36 hours. Severe "splitting"headache (front to back). Nausea. Vomited once the following morning. Fatigue, stiffness, weakness in legs and arms. Worst adverse events from vax 3. Chills began 8 hrs post vax, fever ran from 101 to 102.5 thought the next54 hours. Severe pain in right shoulder joint to point of immobility for24 hours. Nausea , vomiting twice at 24 hrs post vax and 32 hours post vax. Nausea remains but comes and goes. Too weak to walk down steps until48 hours post vax. Severe pain in hip joints for 48 hours post vax. Severe fatigue for 72 hours post vax.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- None. I slept the entire time except when I woke up to take Tylenol and drink a glass of water, so I was actually too sick to have any tests done
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Idiopathic Hypersomnia, hypothyroidism
- Andere Medikamente
- Wellbutrin, escitolapram, thyroxine, multivitamin, Sunosi, zolpidem ( too sick to take any of these for 3 days afterwards)
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- - / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Injection site erythema
Injection site pain
Injection site swelling
Injection site warmth
Peripheral swelling
Symptomtext
Moderna COVID-19 Vaccine EUA" Sx: Tenderness, Swelling, Erythema, elevated temperature at injection site (Right Deltoid). Swelling spread down right extremity to the hands/fingers.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- Refered to Urgent Care provider for follow-up
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 32,0
- Geschlecht
- M
- Eingang
- 12.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site reaction
Rash
Symptomtext
Exanthematous rash around site of injection that was noticed 2 days after administration of the third dose of Moderna. No rash was noticed after the first two doses of Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site reaction
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 79,0
- Geschlecht
- M
- Eingang
- 10.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Pruritus
Swelling
Symptomtext
Redness, swelling, itching that has continued for one week since administration of vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pruritus
- Hospital-Tage
- -
- Labordaten
- 11/7 examination by physician. Ordered ibuprofen, benadryl ointment/spray and icing. 11/8 examination by physician who saw improvement and ordered continuation of above regimen.
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- Atorvastatin, metropolol, B12, D3, low-dose aspirin, metamucil
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 29,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Chills
Extra dose administered
Fatigue
Myalgia
Pain in extremity
Pyrexia
Symptomtext
Pt. states that after receiving the 3rd Booster of Moderna 11/09/2021, started experiencing symptoms that evening of pain in the left arm, fever (101.3), body chills, muscle aches, and fatigue. No noted Primary visit/communications.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Chills
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- Penicillin, Strawberries, Shellfish
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 10.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Injection site pain
Symptomtext
Sore arm at injection site (left only). Treated with analgesics (night-time only, ibuprofen)
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site pain
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- obesity
- Andere Medikamente
- -
- Allergien
- none
- Vorherige Impfungen
- Moderna, COVID-19 Vaccine 2nd shot. Minor sore arm at inj. site
- Staat
- CA
- Alter
- 41,0
- Geschlecht
- F
- Eingang
- 09.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: nein
Pain
Pyrexia
Urticaria
Symptomtext
24 hours after 2nd shot fever of 101.9 for 24 hrs and extreme body aches. 4 days later hives on face, neck, both arms, hands, and chest.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pain
- Hospital-Tage
- -
- Labordaten
- 11/8/2021 no test just prescribed predniSONE, Benadryl, PEPCID
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 07.11.2021
- Impfdatum
- 04.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Erythema
Injection site erythema
Injection site pruritus
Injection site swelling
Joint swelling
Vaccine positive rechallenge
Symptomtext
Patient reporting itching, redness, and swelling on left upper arm around injection site extending toward her elbow. She received the booster on 11/4/21. The swelling and redness was localized to the injection site until 11/6/21. On the morning of 11/7/21 she noticed that the redness and swelling had moved down to her elbow. She had the same reaction with her 2nd Moderna vaccine as well. I instructed her to use ice, Benadryl and Tylenol to help her be more comfortable and decrease the irritation and swelling, as well as to watch the area and seek medical attention if it got worse.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site erythema
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Atrial Fibrillation
- Andere Medikamente
- Unknown
- Allergien
- None
- Vorherige Impfungen
- Moderna 2nd vaccine.
- Staat
- -
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 06.11.2021
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Feeling hot
Hyperhidrosis
Nausea
Tunnel vision
Symptomtext
Patient received 3rd dose, booster Moderna. Within 30 seconds , patient felt very hot and diaphoretic, tunnel vision and nauseated. Patient transported from chair to wheelchair, then to gurney. Vitals signs taken: BP: 112/69, heart rate 18, O2 sat 97%, temp: 36.7. Patient symptoms started to subside upon lying on gurney for 5 to 10 minutes. Patient given apple juice and tolerated it well. VS taken again upon sitting up. BP: 113/71, heart rate 18, O2 sat 96-97%. Patient verbalized feeling better. Patient symptoms subsided after 40 minutes of observation. Patient able to walk out of the clinic without any problems.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Nausea
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 67,0
- Geschlecht
- M
- Eingang
- 06.11.2021
- Impfdatum
- 03.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Arthralgia
Disturbance in attention
Fatigue
Injection site pain
Nausea
Pain
Symptomtext
Joint and body pain, pain at injection site, fatigue, loss of mental focus, nausea.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Arthralgia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- none
- Andere Medikamente
- -
- Allergien
- Cipro
- Vorherige Impfungen
- -
- Staat
- OK
- Alter
- 78,0
- Geschlecht
- F
- Eingang
- 03.11.2021
- Impfdatum
- 02.11.2021
- Beginn
- 03.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- N/A
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Influenza like illness
Injection site swelling
Symptomtext
visible 4+ inch swollen area around injection site; mild flu-like symptoms
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Injection site swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- TX
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 01.11.2021
- Impfdatum
- 30.10.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Axillary pain
Skin swelling
Symptomtext
PATIENT REPORTS HAVING PAIN IN LEFT ARMPIT AND A BUMP UNDER THE SKIN IN THE SAME LEFT ARM AS VACCINE WAS GIVEN. PATIENT SAID IT STARTED MONDAY MORNING AROUND 9:30AM AND HAS NOT TAKEN ANY MEDICATION OVER THE COUNTER.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Axillary pain
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- diabetes
- Andere Medikamente
- glipizide
- Allergien
- Quinolones
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 85,0
- Geschlecht
- F
- Eingang
- 22.06.2023
- Impfdatum
- 12.11.2021
- Beginn
- 17.05.2023
- Tage bis Beginn
- 551,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Asthenia
COVID-19
Mental status changes
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 5/17/2023 - 5/20/2023 (3 days) Presentation to the ED: weakness and AMS COVID + date: 5/17/2023 Treatment: antiviral remdesivir, bronchodilator therapy and oxygen therapy Discharge to: SNF. 011J20A 1/12/2021 028L20A 2/9/2021 066F21A 11/12/2021
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Asthenia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- CVA, elevated TSH, acute kidney injury, elevated CK
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 05.05.2023
- Impfdatum
- 07.04.2021
- Beginn
- 22.09.2022
- Tage bis Beginn
- 533,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19 immunisation
SARS-CoV-2 test
Suspected COVID-19
Symptomtext
SUSPECTED COVID-19 INFECTION; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a patient via other company (Pfizer Inc.) concerned a 50 year old female. The patient's height, and weight were not reported. The patient's concurrent conditions included: scleroderma, gastroesophageal reflux disease (GERD), and allergy, and other pre-existing medical conditions included: The patient was not pregnant at the time of vaccination and had no history of past drug. The patient stated she was taking other medication or products within 2 weeks of starting covid-19 treatment (Paxlovid). The patient received first dose with covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 041A21A expiry: UNKNOWN) dose was not reported,1 total was administered on 07-APR-2021 to left arm for covid-19 prophylaxis. Age at time of vaccination 49 years old. Concomitant medications included amlodipine, hydroxychloroquine, and xantofyl (Lutein). It was unknown whether patient had any adverse events following vaccination with covid-19 vaccine ad26.cov2.s (Dose number in series 1). The patient additionally received 2 doses (second and third dose) with non-company suspect vaccine Moderna covid-19 vaccine, (elasomeran),(Dose number in series 2), (batch number: 066F21A expiry: UNKNOWN, form of admin, route of admin were not reported) dose was not reported, administered on 06-NOV-2021 to left arm, and (batch number: 065F21A expiry: UNKNOWN, form of admin, route of admin, and were not reported) dose was not reported, administered on 03-DEC-2021 to left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with 2 doses of Moderna covid-19 vaccine (elasomeran) (Dose number in series 2). The patient also received fourth dose with non-company suspect vaccine Pfizer biontech covid-19 vaccine (tozinameran) (Dose number in series 3) (form of admin, route of admin, and were not reported, batch number: FM7553 expiry: UNKNOWN) dose was not reported, administered on 26-MAY-2022 to left arm for covid-19 prophylaxis. It was unknown whether patient had any adverse events following vaccination with Pfizer biontech covid-19 vaccine (tozinameran) (Dose number in series 3). The patient also received fifth dose with non-company suspect vaccine Pfizer biontech covid-19 vaccine (tozinameran) (Dose number in series 4) (form of admin, route of admin, and batch number were not reported) dose was not reported, administered on 22-SEP-2022 for covid-19 prophylaxis which was associated with revaccination with different covid-19 vaccine (Dose number in series 4). On an unspecified date, the patient experienced suspected covid-19 infection (Dose number in series 4). The patient started taking treatment with non-company suspect drug Paxlovid (nirmatrelvir/ritonavir) (form of admin, route of admin, batch number and expiry date were not reported) dose and frequency were not reported from 17-APR-2023 to 22-APR-2023 for treatment of covid-19. On 23-APR-2023, (6 days after first dose of treatment with Paxlovid) and on 25-APR-2023 (8 days after first dose of treatment with Paxlovid), the patient was tested negative for rapid tests (COVID-19 rapid POC tests). On 28-APR-2023, (11 days after first dose of treatment with Paxlovid), symptoms had returned again (covid-19 rebound infection). The action taken with covid-19 vaccine ad26.cov2.s, elasomeran, tozinameran, and tozinameran was not applicable; and action taken with nirmatrelvir/ritonavir was not reported. The outcome of the suspected covid-19 infection and revaccination with different covid-19 vaccine was not reported. This report was non-serious.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 immunisation
- Hospital-Tage
- -
- Labordaten
- Test Date: 20230423; Test Name: COVID-19 RAPID TEST; Test Result: Negative ; Test Date: 20230425; Test Name: COVID-19 RAPID TEST; Test Result: Negative
- Aktuelle Erkrankungen
- Allergy; GERD; Scleroderma
- Vorgeschichte
- Comments: The patient was not pregnant at the time of vaccination and had no history of past drug. The patient stated she was taking other medication or products within 2 weeks of starting covid-19 treatment (Paxlovid).
- Andere Medikamente
- AMLODIPINE; HYDROXYCHLOROQUINE; LUTEIN [XANTOFYL]; PAXLOVID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 21.12.2022
- Impfdatum
- 07.11.2022
- Beginn
- 04.12.2022
- Tage bis Beginn
- 27,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Encephalopathy
SARS-CoV-2 test positive
Symptomtext
Hospitalization: 12/4/2022 - 12/7/2022 (3 days) Presentation to the ED: acute encephalopathy. COVID + date: 12/4/2022 Treatment: IV dexamethasone and Remdesivir Discharge to: Home. 1. Moderna Lot # 030L20A 1/26/2021 2. Moderna Lot # 013M20A 2/23/2021 3. Moderna Lot # 066F21A 11/15/2021 4. Moderna Lot # 056M21A 4/24/2022 5. Moderna BiValent booster Lot # GH9702 11/7/2022
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- dementia, hypertension, afib, pacemaker, malignant neoplasm of the large intestine.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.12.2022
- Impfdatum
- 09.03.2021
- Beginn
- 30.10.2021
- Tage bis Beginn
- 235,0
- Dosis
- 2
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
COVID-19 immunisation
SARS-CoV-2 test
Vaccination failure
Symptomtext
CONFIRMED CLINICAL VACCINATION FAILURE; CONFIRMED COVID-19 INFECTION; REVACCINATION WITH DIFFERENT COVID-19 VACCINE; This spontaneous report received from a consumer via Pfizer concerned a patient of unspecified age, sex, race and ethnicity. Initial information was processed along with additional information on 30-NOV-2022. The patient's height, and weight were not reported. The patient's concurrent conditions included: drug allergy (tincture of benzoin). The patient received covid-19 vaccine ad26.cov2.s (Dose number in series 1) (suspension for injection, route of admin not reported, batch number: 1805020 expiry: UNKNOWN) dose was not reported, 1 total, administered to right arm on 09-MAR-2021 13:00 for covid-19 prophylaxis. Concomitant medications included simvastatin for an unknown indication The patient additionally received non-company suspect covid-19 vaccine (Moderna, Spikevax) elasomeran (Dose number in series 2) (form of admin, route of admin were not reported, batch number: 066F21A, expiry: UNKNOWN) dose was not reported, administered to right arm on 30-OCT-2021 16:00 for covid-19 prophylaxis, which was revaccination with different covid-19 vaccine (Dose number in series 2). It was unknown whether patient had any adverse event post covid-19 vaccine (Moderna, Spikevax) (Dose number in series 2). The patient additionally received non-company suspect covid-19 vaccine (Pfizer biontech covid-19 vaccine) tozinameran (Dose number in series 3) (form of admin, route of admin were not reported, batch number: FP7139 expiry: UNKNOWN) dose was not reported, administered to left arm on 08-AUG-2022 16:00 for covid-19 prophylaxis. On an unspecified date, the patient experienced covid-19 (confirmed covid-19 infection) (Dose number in series 3) and hence confirmed clinical vaccination failure (Dose number in series 1). The patient received non-company suspect Paxlovid (Nirmatrelvir/ritonavir) (form of admin, route of admin were not reported, batch number: unknown, expiry: UNKNOWN) dose was not reported, administered from 29-OCT-2022 to 02-NOV-2022 for covid-19 treatment. On 04-NOV-2022, 2 days after completion of Paxlovid, the patient tested negative for covid via Home Binax Now test. On 05-NOV-2022, Laboratory data included: COVID-19 virus test Negative. On 06-NOV-2022, Laboratory data included: COVID-19 virus test Negative. On 07-NOV-2022, Laboratory data included: COVID-19 virus test Negative. On 08-NOV-2022, at 07:00 the patient tested positive and symptoms returned, symptoms included headache, chills, congestion, tightness in chest and cough. Laboratory data included: COVID-19 virus test Positive. The action taken with covid-19 vaccine ad26.cov2.s, elasomeran, and tozinameran was not applicable and with paxlovid treatment discontinued. The patient had not recovered from confirmed covid-19 infection, and the outcome of confirmed clinical vaccination failure and revaccination with different covid-19 vaccine was not reported. This report was serious (Other Medically Important Condition). This report was associated with product quality complaint: 90000261269.; Sender's Comments: V0: 20221163593-confirmed clinical vaccination failure. The event has a compatible/suggestive temporal relationship, is unlabeled, and has unknown scientific plausibility. There are other factors more likely to be associated with the event. Specifically: SPECIAL SITUATIONS. Therefore, this event is considered inconsistent with vaccine administration.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20221104; Test Name: HOME BINAX NOW TEST; Test Result: Negative ; Test Date: 20221105; Test Name: COVID-19 VIRUS TEST; Test Result: Negative ; Test Date: 20221106; Test Name: COVID-19 VIRUS TEST; Test Result: Negative ; Test Date: 20221107; Test Name: COVID-19 VIRUS TEST; Test Result: Negative ; Test Date: 20221108; Test Name: COVID-19 VIRUS TEST; Test Result: Positive
- Aktuelle Erkrankungen
- Drug allergy (TINCTURE OF BENZOIN)
- Vorgeschichte
- -
- Andere Medikamente
- ZOCOR
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 59,0
- Geschlecht
- F
- Eingang
- 26.11.2022
- Impfdatum
- 23.11.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Biopsy
COVID-19 immunisation
Interchange of vaccine products
Magnetic resonance imaging
Melanoma recurrent
Symptomtext
I received the Moderna booster, then 2 months later was noted on surveillance MRI of another local recurrence; Interchange of vaccine products; Revaccination with different COVID-19 vaccine; This spontaneous case was reported by a physician and describes the occurrence of MELANOMA RECURRENT (I received the Moderna booster, then 2 months later was noted on surveillance MRI of another local recurrence) in a 59-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) for an unknown indication. Patient medical history, concomitant disease, risk factor included melanoma, s/p resection x2. Was treated with Inhibitors of the immune checkpoint inhibitor concomittantly The patient did not had any additional medical history, concomitant disease or risk factor. There were no additional lab data/results available. Concurrent medical conditions included Melanoma. On 23-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) .5 milliliter. On an unknown date, the patient received dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) 1 dosage form. On an unknown date, received dose of TOZINAMERAN (PFIZER BIONTECH COVID-19 VACCINE) (unknown route) dosage was changed to 1 dosage form. On an unknown date, the patient experienced MELANOMA RECURRENT (I received the Moderna booster, then 2 months later was noted on surveillance MRI of another local recurrence) (seriousness criterion medically significant), INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) and COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine). On 21-Feb-2022, MELANOMA RECURRENT (I received the Moderna booster, then 2 months later was noted on surveillance MRI of another local recurrence) had resolved. At the time of the report, INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) and COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Biopsy: Inconclusive. On an unknown date, Magnetic resonance imaging: Inconclusive. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No Concomitant medications were provided. Patient was a physician and received two initial doses of Pfizer 2 months later, patient was found to had a local recurrence of melanoma. It was removed 6 months later. Patient received the Moderna booster, then 2 months later was noted on surveillance MRI of another local recurrence. Medication Details and reason for taking the medicine included surgical resection. Company Comment: This spontaneous case of Interchange of vaccine products concerns a 59-year-old female patient, with relevant medical history of Melanoma, who experienced the unexpected serious (medically significant) event of Melanoma recurrent. The event occurred approximately 2 months after receiving the third dose of mRNA-1273 Vaccine. It was reported that patient received two initial doses of Pfizer. Two months later, patient was found to have a local recurrence of melanoma that was removed 6 months later. After booster dose of Moderna, patient was noted on surveillance MRI to have another local recurrence. Diagnostic tests - MRI and Biopsy were reported as inconclusive. Treatment included surgical resection. The outcome of the event was reported as resolved. The patient's medical history of Melanoma (with recurrence after Pfizer vaccination) remain as a confounder for the occurrence of the event. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.; Sender's Comments: This spontaneous case of Interchange of vaccine products concerns a 59-year-old female patient, with relevant medical history of Melanoma, who experienced the unexpected serious (medically significant) event of Melanoma recurrent. The event occurred approximately 2 months after receiving the third dose of mRNA-1273 Vaccine. It was reported that patient received two initial doses of Pfizer. Two months later, patient was found to have a local recurrence of melanoma that was removed 6 months later. After booster dose of Moderna, patient was noted on surveillance MRI to have another local recurrence. Diagnostic tests - MRI and Biopsy were reported as inconclusive. Treatment included surgical resection. The outcome of the event was reported as resolved. The patient's medical history of Melanoma (with recurrence after Pfizer vaccination) remain as a confounder for the occurrence of the event. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Biopsy
- Hospital-Tage
- -
- Labordaten
- Test Name: Biopsy test; Test Result: Inconclusive ; Test Name: MRI; Test Result: Inconclusive
- Aktuelle Erkrankungen
- Melanoma
- Vorgeschichte
- Comments: Patient medical history, concomitant disease, risk factor included melanoma, s/p resection x2. Was treated with Inhibitors of the immune checkpoint inhibitor concomittantly The patient did not had any additional medical history, concomitant disease or risk factor. There were no additional lab data/results available.
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 64,0
- Geschlecht
- M
- Eingang
- 09.11.2022
- Impfdatum
- 03.12.2021
- Beginn
- 15.01.2022
- Tage bis Beginn
- 43,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
Amyotrophic lateral sclerosis
Electromyogram
Limb immobilisation
Magnetic resonance imaging
Muscular weakness
Peripheral nerve decompression
Symptomtext
Weakness in left index finger and thumb, followed by complete immobiliy of left hand, followed by no improvement for months, followed by EMG and cubital tunnel release on 8-16-2022 with no improvement in hand mobility, followed by patient of Neurosciences Clinic 10-5-22, followed by MRI and EMG at Univ. Utah on 10-28-22, followed by diagnosis of probable ALS, sent to Neurosciences ALS Clinic 11-30-2022.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Amyotrophic lateral sclerosis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- type 1 diabetes for 48 years
- Andere Medikamente
- novolog, tresiba, quinapril, levothyroxin, B12 complex, omega3
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 83,0
- Geschlecht
- M
- Eingang
- 08.11.2022
- Impfdatum
- 22.11.2021
- Beginn
- 27.10.2022
- Tage bis Beginn
- 339,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Admitted to hospital
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 5,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 20.10.2022
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: ja
ER: unbekannt
Erholt: nein
COVID-19 immunisation
Interchange of vaccine products
Rheumatoid arthritis
Symptomtext
Seronegative rheumatoid arthritis; Revaccination with different COVID-19 vaccine; Interchange of vaccine products; This spontaneous case was reported by a physician and describes the occurrence of RHEUMATOID ARTHRITIS (Seronegative rheumatoid arthritis) in a 30-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19. The occurrence of additional non-serious events is detailed below. Previously administered products included for Product used for unknown indication: Pfizer (Dose Number: 1 Batch/Lot No: EK5730 Anatomical location: Left arm Route of Administration: Intramuscular) on 21-Dec-2020 and Pfizer (Dose Number: 2 Batch/Lot No: EL3246 Anatomical location: Left arm Route of Administration: Intramuscular) on 11-Jan-2021. Past adverse reactions to the above products included No adverse event with Pfizer and Pfizer. Concurrent medical conditions included Drug allergy (Unknown historical drug). On 19-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular) 1 dosage form. On 19-Nov-2021, the patient experienced COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products). On 25-Jan-2022, the patient experienced RHEUMATOID ARTHRITIS (Seronegative rheumatoid arthritis) (seriousness criteria disability and medically significant). The patient was treated with METHOTREXATE at an unspecified dose and frequency and PREDNISONE at an unspecified dose and frequency. On 19-Nov-2021, COVID-19 IMMUNISATION (Revaccination with different COVID-19 vaccine) and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) had resolved. At the time of the report, RHEUMATOID ARTHRITIS (Seronegative rheumatoid arthritis) had not resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Intramuscular), the reporter did not provide any causality assessments. No concomitant medication information was provided. Events Arthritis and Hand deformity subsumed under the event Rheumatoid arthritis The patient was not diagnosed with COVID-19. It was unknown the patient had been tested for COVID-19 since the vaccination Device Date : 13-Oct-2022 Company Comment: This is a spontaneous case concerning a 30 year-old, male patient with no reported medical history, who experienced the serious (due to medically important condition and disability) unexpected, AESI of Rheumatoid arthritis, which occurred approximately 2 months after the mRNA-1273 vaccine, received as the third dose of COVID-19 vaccination schedule. Patient reported Inflammatory joints and hand deformities and was diagnosed as seronegative rheumatoid arthritis. He received treatment with Methotrexate and Prednisone. The outcome was reported as not recovered. Additionally, Interchange of vaccine products and Revaccination with different COVID-19 vaccine (vaccination with two doses of COVID-19 vaccine Tozinameran) was noted in the case. No further clinical information was available for medical review. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This is a spontaneous case concerning a 30 year-old, male patient with no reported medical history, who experienced the serious (due to medically important condition and disability) unexpected, AESI of Rheumatoid arthritis, which occurred approximately 2 months after the mRNA-1273 vaccine, received as the third dose of COVID-19 vaccination schedule. Patient reported Inflammatory joints and hand deformities and was diagnosed as seronegative rheumatoid arthritis. He received treatment with Methotrexate and Prednisone. The outcome was reported as not recovered. Additionally, Interchange of vaccine products and Revaccination with different COVID-19 vaccine (vaccination with two doses of COVID-19 vaccine Tozinameran) was noted in the case. No further clinical information was available for medical review. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19 immunisation
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Drug allergy (Unknown historical drug)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 17.09.2022
- Impfdatum
- 17.09.2021
- Beginn
- 05.09.2022
- Tage bis Beginn
- 353,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Unevaluable event
Symptomtext
Admitted to hospital.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- 4,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 82,0
- Geschlecht
- U
- Eingang
- 12.09.2022
- Impfdatum
- 16.11.2021
- Beginn
- 07.09.2022
- Tage bis Beginn
- 295,0
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Symptomtext
HOSPITALIZED WITH COVID
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- 3,0
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 07.07.2022
- Impfdatum
- 27.11.2021
- Beginn
- 27.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
Symptomtext
Patient developed COVID-19 post vaccinations.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 03.07.2022
- Impfdatum
- 08.04.2021
- Beginn
- 14.11.2021
- Tage bis Beginn
- 220,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
Interchange of vaccine products
Nucleic acid test
SARS-CoV-2 test
Symptomtext
Experienced COVID-19 symptoms/COVID -19 infection; Interchange of vaccine products; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (Experienced COVID-19 symptoms/COVID -19 infection) in a 44-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for Prophylactic vaccination. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) for Prophylactic vaccination. Concurrent medical conditions included Allergy. On 08-Apr-2021, the patient received first dose of COVID-19 VACCINE NRVV AD26 (JNJ 78436735) (JANSSEN COVID-19 VACCINE) (unknown route) 1 dosage form. On 14-Nov-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 14-Nov-2021, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products). On 10-May-2022, the patient experienced COVID-19 (Experienced COVID-19 symptoms/COVID -19 infection) (seriousness criterion medically significant). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 11-May-2022 to 16-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, COVID-19 (Experienced COVID-19 symptoms/COVID -19 infection) had not resolved and INTERCHANGE OF VACCINE PRODUCTS (Interchange of vaccine products) outcome was unknown. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 11-May-2022, Nucleic acid test: positive (Positive) Positive. On 20-May-2022, SARS-CoV-2 test: negative (Negative) Negative. On 23-May-2022, SARS-CoV-2 test: positive (Positive) Positive. The age at the time of COVID-19 vaccine Janssen was 43 years. The date of birth of patient was reported as unknown date Jun-1977. No concomitant medication was provided by reporter. On 10-May-2022 approximately 13 months after Janssen vaccine, clinical vaccine failure happened. For Janssen, reporter causality was possible, causality as per Mfr. was possible. This report was associated with product quality complaint: 90000234197 Company comment-This spontaneous case concerns a male patient aged 44 years with no relevant medical history reported, who experienced the unexpected serious medically significant AESI of Covid 19 approximately 177 days after receiving a dose (2nd dose) of mRNA-1273 vaccine in the covid 19 vaccination series. Additionally Interchange of vaccine products was noted as patient had received a dose of vaccination with co suspect JANSSEN COVID-19 VACCINE 220 days prior to current vaccination. Patient had initial covid -19 symptoms, next day Nucleic acid amplification test was positive, started treatment with Paxlovid for 6 days. Outcome of the event Covid 19 was not resolved at the time of report. The current pandemic situation of COVID 19 may remain as confounder to the event Covid-19. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Event seriousness assessed as per medical judgement.; Sender's Comments: This spontaneous case concerns a male patient aged 44 years with no relevant medical history reported, who experienced the unexpected serious medically significant AESI of Covid 19 approximately 177 days after receiving a dose (2nd dose) of mRNA-1273 vaccine in the covid 19 vaccination series. Additionally Interchange of vaccine products was noted as patient had received a dose of vaccination with co suspect JANSSEN COVID-19 VACCINE 220 days prior to current vaccination. Patient had initial covid -19 symptoms, next day Nucleic acid amplification test was positive, started treatment with Paxlovid for 6 days. Outcome of the event Covid 19 was not resolved at the time of report. The current pandemic situation of COVID 19 may remain as confounder to the event Covid-19. The benefit-risk relationship of mRNA-1273 Vaccine is not affected by this report. Event seriousness assessed as per medical judgement.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220511; Test Name: Nucleic acid amplification tests; Test Result: Positive ; Result Unstructured Data: Positive; Test Date: 20220520; Test Name: COVID-19 antigen test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220523; Test Name: COVID-19 antigen test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Allergy
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 80,0
- Geschlecht
- M
- Eingang
- 14.06.2022
- Impfdatum
- 07.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Lot # expiration date had been extended. Vaccine had remained in the freezer until date of administration but was given 4 days past expiration date. Moderna was consulted and they deemed the vaccine viable so revaccination was not necessary. No adverse side effects were reported by the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Expiration date for the lot# had been extended, vaccine remained frozen until date of administration. Vaccine was given 2 days past expiration date. Moderna consulted and deemed the vaccine viable so revaccination is not necessary. No adverse side effects were reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 77,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Lot # had extended expiration date and vaccine had remained frozen until date of administration but was given 2 days past expiration date. Moderna consulted and deemed the vaccine viable so revaccination was not necessary. No adverse side effects were reported from patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Lot # expiration date had been extended and vaccine remained frozen until date of administration. Vaccine was given 2 days past expiration date. Moderna consulted and deemed the vaccine viable so revaccination was not necessary. No adverse side effects were reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Expiration date for lot # had been extended and vaccine had remained frozen until date of administration. Vaccine was given 2 days past expiration date. Moderna consulted and deemed the vaccine viable so revaccination is not necessary. No adverse side effects were reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 61,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Expiration for that lot # had been extended and vaccine remained frozen until date of administration but vaccine was given 2 days past expiration date. Moderna consulted and deemed the vaccine viable so revaccination was not necessary. No adverse side effects were reported from patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Expiration date for vaccine lot 3 had been extended and vaccine remained frozen until date of administration. Vaccine was given 2 days past expiration date. Moderna consulted and deemed the vaccine viable so revaccination was not necessary. No adverse effects were reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 90,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Lot 3 expiration had been extended and vaccine had remained in freezer until date of administration. Vaccine was given 2 days past expiration date. Moderna was consulted and deemed the vaccine viable so revaccination was not necessary. No adverse side effects were reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 83,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Vaccine had extended lot # and had remained frozen until date of administration. vaccine was given 2 days past expiration date. Moderna consulted and deemed the vaccine viable so revaccination was not necessary. No adverse side effects were reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 73,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Expiration date for lot # had been extended and vaccine had remained in the freezer until date of administration but was administered 2 days past expiration date. Moderna consulted and deemed the vaccine viable so revaccination was not necessary. No adverse side effects were reported by the patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 88,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Lot # exp had been extended and vaccine remained frozen until date of administration but was given 2 days past exp date. Moderna consulted and deemed the vaccine viable so no revaccination was needed. No adverse side effects were reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 82,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Vaccine lot # had been extended and vaccine had remained frozen until date of administration but was given 2 days after expiration date. Moderna consulted and deemed the vaccine viable so revaccination was not necessary. no adverse side effects were reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WY
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Lot # expiration had been extended and vaccine had remained frozen until date of administration but was given 2 days past expiration date. Moderna consulted and deemed the vaccine viable so revaccination was not necessary. No adverse side effects reported by Patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 70,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Lot # exp date had been extended and vaccine remained frozen until date of administration. Vaccine was given 2 days past expiration date. Modena consulted and they deemed the vaccine viable so revaccination was not needed. No adverse side effects were reported by Patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 84,0
- Geschlecht
- U
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Lot # had been extended and vaccine had remained in freezer until date of administration. Vaccine was given 2 days after exp. date. Moderna consulted and deemed the vaccine still viable so revaccination was not neccesary. No adverse effects reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 71,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Lot # expiration had been extended and vaccine had remained in freezer until day of administration. Vaccine was given 2 days past expiration date, Moderna consulted and they deemed the vaccine viable so revaccination was not required. No adverse effects reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Lot # expiration had been extended. Vaccine remained frozen until date of administration but accidentally given 2 days past expiration. Moderna was consulted and they deemed the vaccine still viable so revaccination was not necessary. No adverse side effects were reported by patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Vaccine lot # had been extended and had remained frozen until date of administration. Was given 2 days post expiration date. Moderna consulted and they deemed the vaccine still viable so revaccination was not required. Patient did not report any adverse side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- IA
- Alter
- 92,0
- Geschlecht
- M
- Eingang
- 13.06.2022
- Impfdatum
- 05.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Vaccine lot # had been extended and had remained frozen until date of administration but was administered 2 days past expiration date. Moderna consulted and they deemed the vaccine still viable so no revaccination was required. Pt did not report any adverse side effects.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- FL
- Alter
- 75,0
- Geschlecht
- F
- Eingang
- 13.06.2022
- Impfdatum
- 07.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Symptomtext
Vaccine expiration date was extended to 4/3/22 and had been kept frozen up until date of administration which was 4/7/22. Moderna contacted and Moderna advised that vaccine was still viable and no revaccination was necessary. No adverse side effects were reported from patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- F
- Eingang
- 11.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not reported. Expired vaccine was administered to total of 24 patients including 15 males and 9 females. It was reported administrations were mostly for booster shots. No side effects were reported. Treatment medication was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 11.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments.* No concomitant medication was reported. It was reported that vaccine was administered to total of 24 patients including 15 males and 9 females. HCP reported administrations were mostly for booster shots. No side effects reported. No treatment information were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medications were reported. HCP reported vial with lot(066F21A) which was expired on 3-Apr-2022.was administered to total of 24 patients including 15 males and 9 females. HCP reports administrations were mostly for booster shots. No side effects was reported No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. It was reported that the administrations were done mostly for booster shots. No side effects were reported. No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Vial which was expired on 3Apr2022 was administered to patients; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Vial which was expired on 3Apr2022 was administered to patients) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Vial which was expired on 3Apr2022 was administered to patients). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Vial which was expired on 3Apr2022 was administered to patients) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication information was provided by the reporter. Expired vaccine was administered to total of 24 patients including 15 males and 9 females. It was reported administrations were mostly for booster shots. No side effects were reported for the patient. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medications were provided. It was reported that total of 24 patients including 15 males and 9 females were administered expired vaccine which were mostly for booster shots. No other side effects were reported. No treatment medications were provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product was provided by the reporter. Reported that no side effects was reported . No treatment medication was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. No side effects was reported. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications was reported. No treatment information was reported It was reported that vaccine administered to total of 24 patients including 15 males and 9 females. HCP reports administrations were mostly for booster shots. No side effects was reported. .
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication was not reported. Expired vaccine was administered to total of 24 patients including 15 males and 9 females. It was reported administrations were mostly for booster shots. No side effects were reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that vaccine was administered to total of 24 patients including 15 males and 9 females and were mostly for booster shots. No side effects was reported No concomitant medications were reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant product use was reported. The reporter stated that the patient was administered booster shot from the vial which was expired on 3-Apr-2022. No side effects were reported. No treatment information was provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
vial with lot(066F21A) which was expired on 3-Apr-2022 was administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vial with lot(066F21A) which was expired on 3-Apr-2022 was administered) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (vial with lot(066F21A) which was expired on 3-Apr-2022 was administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vial with lot(066F21A) which was expired on 3-Apr-2022 was administered) 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 details were reported. No side effects were reported after vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- F
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a female patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant drugs were not reported. It was reported that total of 24 patients including 15 males and 9 females were administered expired vaccine which were mostly for booster shots. No other side effects were reported. Treatment medications were not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- 03.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On 03-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were provided by the reporter. It was reported that vaccine expired on 3 Apr 2022 was administered to total of 24 patients including 15 males and 9 females. The administrations were mostly for booster shots. No side effects was reported. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Vaccine was administered to total of 24 patients including 15 males and 9 females. HCP reported administrations were mostly for booster shots. No side effects 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
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medications were reported. Expired vaccine was administered to total 24 patients including 15 males and 9 females. It was reported that administrations were mostly for booster shots. No side effects were reported for the patient. 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
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that vaccine administered to total 24 patients including 15 males and 9 females, mostly for booster shots. No side effects was reported. No concomitant medications was reported. No treatment medications was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that vaccine administered to total 24 patients including 15 males and 9 females. No concomitant medications was reported. HCP reported administrations were mostly for booster shots. No treatment medications was reported. No side effects was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. It was reported that vaccine administered to total of 24 patients including 15 males and 9 females, mostly for booster shots. No side effects was reported No concomitant medication was reported. No treatment medication was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
vial which was expired on 3-Apr-2022 was administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (vial which was expired on 3-Apr-2022 was administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (vial which was expired on 3-Apr-2022 was administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (vial which was expired on 3-Apr-2022 was administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant product use was not provided by the reporter. It was reported that a vial which had expired on 03-Apr-2022 was administered to total of 24 patients which included 15 males and 9 females, the administrations were mostly for booster shots and no side effects were reported. Treatment information was not provided.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant drug was reported. It was reported that vial that was expired on 03-Apr-2022 was administered to total of 24 patients including 15 males and 9 females. Health care professional reported administrations were mostly for booster shots. No side effects was reported. No treatment drug was reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. Concomitant medication of the patient was not reported. Expired vaccine was administered to total of 24 patients including 15 males and 9 females. It was reported administrations were mostly for booster shots. No side effects were reported for the patient. No treatment information was provided by the reporter.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- -
- Geschlecht
- M
- Eingang
- 10.06.2022
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Symptomtext
Expired vaccine administered; This spontaneous case was reported by a nurse and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) in a male patient of an unknown age who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On an unknown date, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On an unknown date, the patient experienced EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered). At the time of the report, EXPIRED PRODUCT ADMINISTERED (Expired vaccine administered) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. It was reported that vaccine was administered to total of 24 patients including 15 males and 9 females. HCP reported administrations were mostly for booster shots. No side effects reported. No treatment information were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 89,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 07.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 4
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
No adverse event
Product storage error
Symptomtext
Vaccine had expiration date of 4/3/22 but was kept frozen until date of administration. Moderna contacted and deemed the vaccine viable and repeat dose not needed. No adverse event to report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 80,0
- Geschlecht
- F
- Eingang
- 09.06.2022
- Impfdatum
- 07.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine had expired on 4/3/22. Moderna was contacted and since vaccine had been frozen up until date of administration, it was deemed viable and redosing was not needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- AS
- Alter
- 33,0
- Geschlecht
- M
- Eingang
- 09.06.2022
- Impfdatum
- 07.04.2022
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Expired product administered
Symptomtext
Vaccine had expired on 4/3/22. Moderna was contacted and since vaccine had been frozen up until date of administration, it was deemed viable and redosing was not needed.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- -
- Geschlecht
- U
- Eingang
- 02.06.2022
- Impfdatum
- 18.11.2021
- Beginn
- 25.05.2022
- Tage bis Beginn
- 188,0
- Dosis
- 3
- Route/Site
- OT / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysgeusia
Symptomtext
Bad / metallic taste for a few hours after taking a dose; This spontaneous case was reported by a consumer and describes the occurrence of DYSGEUSIA (Bad / metallic taste for a few hours after taking a dose) in a patient of an unknown age and gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. Co-suspect product included non-company product NIRMATRELVIR, RITONAVIR (PAXLOVID) for COVID-19 treatment. Previously administered products included for Product used for unknown indication: Pfizer / BioNTech (Dose Number: 2 Batch/Lot No: EW0153 Location of injection: Arm Left) on 07-Apr-2021 and Pfizer / BioNTech (Dose Number: 1 Batch/Lot No: EP7534 Location of injection: Arm Left) on 17-Mar-2022. Past adverse reactions to the above products included No adverse event with Pfizer / BioNTech and Pfizer / BioNTech. Concurrent medical conditions included Allergy (No product reported). On 18-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 25-May-2022, the patient started NIRMATRELVIR, RITONAVIR (PAXLOVID) (unknown route) at an unspecified dose. On 25-May-2022, after starting mRNA-1273 (Moderna COVID-19 Vaccine), the patient experienced DYSGEUSIA (Bad / metallic taste for a few hours after taking a dose). At the time of the report, DYSGEUSIA (Bad / metallic taste for a few hours after taking a dose) outcome was unknown. No concomitant medications were reported. Patient was not taking any other medications/products within 2 weeks of starting COVID-19 treatment. Device Date was reported as 27-May-2022 No treatment medications were reported.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysgeusia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Allergy (No product reported.)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 44,0
- Geschlecht
- M
- Eingang
- 31.05.2022
- Impfdatum
- 14.11.2021
- Beginn
- 11.05.2022
- Tage bis Beginn
- 178,0
- Dosis
- 2
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
COVID-19
Nucleic acid test
SARS-CoV-2 test
Symptomtext
Initial covid symptoms 5/10 (positive NAAT (Cue) test 5/11), started paxlovid on 5/11. Symptom free by 5/14/ Mild cold-like symptoms starting again 5/22, positive antigen test 5/23.; This spontaneous case was reported by a patient and describes the occurrence of COVID-19 (Initial covid symptoms 5/10 (positive NAAT (Cue) test 5/11), started paxlovid on 5/11. Symptom free by 5/14/ Mild cold-like symptoms starting again 5/22, positive antigen test 5/23.) in a 44-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: Janssen (Dose No 1; Batch No 201A21A; Location Arm Left.) on 08-Apr-2021. Past adverse reactions to the above products included No adverse event with Janssen. Concurrent medical conditions included Allergy. Concomitant products included NIRMATRELVIR, RITONAVIR (PAXLOVID) from 11-May-2022 to 16-May-2022 for COVID-19 treatment. On 14-Nov-2021, the patient received second dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-May-2022, the patient experienced COVID-19 (Initial covid symptoms 5/10 (positive NAAT (Cue) test 5/11), started paxlovid on 5/11. Symptom free by 5/14/ Mild cold-like symptoms starting again 5/22, positive antigen test 5/23.). On 14-May-2022, COVID-19 (Initial covid symptoms 5/10 (positive NAAT (Cue) test 5/11), started paxlovid on 5/11. Symptom free by 5/14/ Mild cold-like symptoms starting again 5/22, positive antigen test 5/23.) had resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 11-May-2022, Nucleic acid test: positive (Positive) positive. On 20-May-2022, SARS-CoV-2 test: negative (Negative) Negative. On 23-May-2022, SARS-CoV-2 test: positive (Positive) positive. No treatment information was reported. The patient had initial COVID symptoms on 10-May. He was symptom free on 14-May. Mild cold-like symptoms started again on 22-May. Company comment: This spontaneous case concerns a 44 year-old male patient, with no medical history reported, who experienced the unexpected, non-serious Adverse Event of Special Interest of COVID-19, which occurred 178 days after a dose of mRNA-1273 vaccine administration, given as the second dose. Patient was previously vaccinated with a dose of Janssen COVID-19 vaccine, with no adverse events reported, 220 days prior to the administration of mRNA-1273 as second dose (Interchange of vaccine products). Patient was started on Paxlovid and was symptom-free after 3 days. Eight days later, mild cold-like symptoms were reported by the patient. Patient again test positive for Sars-CoV-2 the day after. The ongoing COVID-19 pandemic could be a confounder for the event. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.; Sender's Comments: This spontaneous case concerns a 44 year-old male patient, with no medical history reported, who experienced the unexpected, non-serious Adverse Event of Special Interest of COVID-19, which occurred 178 days after a dose of mRNA-1273 vaccine administration, given as the second dose. Patient was previously vaccinated with a dose of Janssen COVID-19 vaccine, with no adverse events reported, 220 days prior to the administration of mRNA-1273 as second dose (Interchange of vaccine products). Patient was started on Paxlovid and was symptom-free after 3 days. Eight days later, mild cold-like symptoms were reported by the patient. Patient again test positive for Sars-CoV-2 the day after. The ongoing COVID-19 pandemic could be a confounder for the event. The benefit-risk relationship of mRNA-1273 vaccine is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Date: 20220511; Test Name: NAAT (Cue) test; Test Result: Positive ; Result Unstructured Data: positive; Test Date: 20220520; Test Name: Antigen test; Test Result: Negative ; Result Unstructured Data: Negative; Test Date: 20220523; Test Name: Antigen test; Test Result: Positive ; Result Unstructured Data: positive
- Aktuelle Erkrankungen
- Allergy
- Vorgeschichte
- -
- Andere Medikamente
- PAXLOVID
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 25.05.2022
- Impfdatum
- 01.11.2021
- Beginn
- 20.02.2022
- Tage bis Beginn
- 111,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Blood iron decreased
Full blood count
Haemoglobin decreased
Iron deficiency anaemia
Serum ferritin decreased
Symptomtext
Iron deficiency anemia. HGB dropped from 13.1 to 9.9 Ferritin level 5
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Blood iron decreased
- Hospital-Tage
- -
- Labordaten
- 2/20/22 CBC, Fe and Ferritin
- Aktuelle Erkrankungen
- mild gastritis
- Vorgeschichte
- Peripheral neuropathy
- Andere Medikamente
- estradiol patch, progesterone , Omeprazole, Vit D, Elderberry
- Allergien
- Flexeril
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 21.05.2022
- Impfdatum
- 12.11.2021
- Beginn
- 12.05.2022
- Tage bis Beginn
- 181,0
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
COVID-19
SARS-CoV-2 test
Symptomtext
COVID-19; Experienced rebound symptoms positive antigen test 4 days after completing Paxlovid treatment; This spontaneous case was reported by a consumer and describes the occurrence of COVID-19 (Experienced rebound symptoms positive antigen test 4 days after completing Paxlovid treatment) and COVID-19 (COVID-19) in a 38-year-old male patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. Concurrent medical conditions included Allergy NOS (unknown historical drug). On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-May-2022, the patient experienced COVID-19 (Experienced rebound symptoms positive antigen test 4 days after completing Paxlovid treatment). On an unknown date, the patient experienced COVID-19 (COVID-19). The patient was treated with NIRMATRELVIR, RITONAVIR (PAXLOVID) from 03-May-2022 to 08-May-2022 for COVID-19 treatment, at an unspecified dose and frequency. At the time of the report, COVID-19 (Experienced rebound symptoms positive antigen test 4 days after completing Paxlovid treatment) and COVID-19 (COVID-19) had not resolved. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On 05-May-2022, SARS-CoV-2 test: negative (Negative) Tested antigen negative 2 days after beginning Paxlovid treatment.. On 12-May-2022, SARS-CoV-2 test: positive (Positive) Positive. On an unknown date, SARS-CoV-2 test: positive (Positive) Positive. No concomitant medications was provided by the reporter. No treatment medications was provided by the reporter. the patient did not take any other medications/products within 2 weeks of starting COVID-19 treatment and the patient previously received a COVID-19 Vaccine. Device Date: 14 May 2022 Company comment: This spontaneous case concerns a 38 year old male patient with no reported medical history who experienced the unexpected, non-serious adverse event of special interest of COVID-19 (reported twice- 1. LLT of COVID-19 and 2. LLT of COVID-19 Recurrent). The event COVID-19 (LLT COVID-19) occurred at an unspecified date after receiving a dose of mRNA1273 as third dose of COVID-19 vaccine, the second event of COVID-19 (LLT COVID-19 recurrent) occurred 6 months post vaccination. The patient tested positive on the COVID-19 antigen test (at an unknown date) and was treated with Nirmatrelvir and Ritonavir (Paxlovid) for 5 days at an unspecified dose and frequency. He experienced rebound symptoms and tested positive for COVID-19 antigen 4 days after completing Paxlovid treatment. The patient did not take any other medications or products within 2 weeks of starting COVID-19 treatment. The events are not yet resolved at the time of this report. The benefit-risk relationship of mRNA-1273 is not affected by this report.; Sender's Comments: This spontaneous case concerns a 38 year old male patient with no reported medical history who experienced the unexpected, non-serious adverse event of special interest of COVID-19 (reported twice- 1. LLT of COVID-19 and 2. LLT of COVID-19 Recurrent). The event COVID-19 (LLT COVID-19) occurred at an unspecified date after receiving a dose of mRNA1273 as third dose of COVID-19 vaccine, the second event of COVID-19 (LLT COVID-19 recurrent) occurred 6 months post vaccination. The patient tested positive on the COVID-19 antigen test (at an unknown date) and was treated with Nirmatrelvir and Ritonavir (Paxlovid) for 5 days at an unspecified dose and frequency. He experienced rebound symptoms and tested positive for COVID-19 antigen 4 days after completing Paxlovid treatment. The patient did not take any other medications or products within 2 weeks of starting COVID-19 treatment. The events are not yet resolved at the time of this report. The benefit-risk relationship of mRNA-1273 is not affected by this report.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- Test Name: COVID-19 antigen test; Test Result: Positive ; Result Unstructured Data: Positive; Test Date: 20220505; Test Name: COVID-19 antigen test; Test Result: Negative ; Result Unstructured Data: Tested antigen negative 2 days after beginning Paxlovid treatment.; Test Date: 20220512; Test Name: COVID-19 antigen test; Test Result: Positive ; Result Unstructured Data: Positive
- Aktuelle Erkrankungen
- Allergy NOS (unknown historical drug)
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 29,0
- Geschlecht
- U
- Eingang
- 19.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Expired product administered
Product storage error
Symptomtext
Manufacture date of expiry 3-apr-2022 , Vial stored in the refrigerator 15-Apr-2022 .; I administered 2 doses of expired Moderna Covid-19 vaccine on 15Apr2022.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (I administered 2 doses of expired Moderna Covid-19 vaccine on 15Apr2022.) and PRODUCT STORAGE ERROR (Manufacture date of expiry 3-apr-2022 , Vial stored in the refrigerator 15-Apr-2022 .) in a 29-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Apr-2022, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 15-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (I administered 2 doses of expired Moderna Covid-19 vaccine on 15Apr2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Manufacture date of expiry 3-apr-2022 , Vial stored in the refrigerator 15-Apr-2022 .). At the time of the report, EXPIRED PRODUCT ADMINISTERED (I administered 2 doses of expired Moderna Covid-19 vaccine on 15Apr2022.) and PRODUCT STORAGE ERROR (Manufacture date of expiry 3-apr-2022 , Vial stored in the refrigerator 15-Apr-2022 .) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant product was provided by the reporter. No treatment medication was provided. The vial did not undergo any temperature excursion.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 55,0
- Geschlecht
- U
- Eingang
- 19.05.2022
- Impfdatum
- 15.04.2022
- Beginn
- 15.04.2022
- 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
manufacturer date of expiry 3-apr-2022 and vail initialy stored in refrigerator on 15-apr-2022; I administered 2 doses of expired Moderna Covid-19 vaccine on 15Apr2022.; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (I administered 2 doses of expired Moderna Covid-19 vaccine on 15Apr2022.) and PRODUCT STORAGE ERROR (manufacturer date of expiry 3-apr-2022 and vail initialy stored in refrigerator on 15-apr-2022) in a 55-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On 15-Apr-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) .25 milliliter. On 15-Apr-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (I administered 2 doses of expired Moderna Covid-19 vaccine on 15Apr2022.). On an unknown date, the patient experienced PRODUCT STORAGE ERROR (manufacturer date of expiry 3-apr-2022 and vail initialy stored in refrigerator on 15-apr-2022). At the time of the report, EXPIRED PRODUCT ADMINISTERED (I administered 2 doses of expired Moderna Covid-19 vaccine on 15Apr2022.) and PRODUCT STORAGE ERROR (manufacturer date of expiry 3-apr-2022 and vail initialy stored in refrigerator on 15-apr-2022) outcome was unknown. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The vial did not undergone any temperature excursion. No treatment medication was reported. It was unknown if patient had allergies to medications, food and other products. It was unknown if patient ever had COVID positive test or diagnosis. It was unknown if patient had history relating to mentioned AE and both Acute and Chronic illnesses at the time of vaccination.Other vaccines given within 1 month prior to Moderna COVID-19 vaccine were unknown.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 39,0
- Geschlecht
- F
- Eingang
- 09.05.2022
- Impfdatum
- 03.12.2021
- Beginn
- 05.05.2022
- Tage bis Beginn
- 153,0
- Dosis
- 3
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Vaccine breakthrough infection
Symptomtext
COVID breakthrough case
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- COVID positive test 05/07/2022
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 47,0
- Geschlecht
- F
- Eingang
- 01.05.2022
- Impfdatum
- 01.02.2021
- Beginn
- 01.03.2021
- Tage bis Beginn
- 28,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
swollen lymph nodes R axilla,
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- mammograms, ultrasound and punch biopsy in L axilla, next follow up mammogram due in 6 months
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- HTN, eczema
- Andere Medikamente
- HCTZ, Kelnor, Zyrtec, Women's MVI
- Allergien
- Latex
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 68,0
- Geschlecht
- F
- Eingang
- 21.04.2022
- Impfdatum
- 11.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Unevaluable event
Symptomtext
Client presented at the vaccination site on 11.11.21. Client reported she received 1st dose Moderna COVID vaccine on 04.14.21 and 2nd dose Moderna COVID vaccine on 05.12.21, both are from vaccination site without any symptoms for both doses. Client is requesting to receive her Moderna COVID booster vaccine today one day earlier than she is qualifies for the Moderna COVID booster vaccine. Client reported she doesn?t have any known allergies or have any chronic illnesses. Client told she is not taking any medications. PHN submitted a medical consult via text message to clinical project coordinator, requesting to proceed with the Moderna COVID booster vaccine. Per the doctor, approval to proceed with Moderna COVID booster vaccine was obtained from medical consult team via text message from clinical project coordinator. Client received Moderna COVID booster vaccine, LOT #: 066F21A on 11.11.21 at 1511 by RN. The client did not report any symptoms during the 30-minute observation period. PHN educated client on possible adverse reactions and when to seek EMS. Client verbalized understanding. Client left vaccination site at 1541 unassisted and with a steady gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Unevaluable event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 14.03.2022
- Impfdatum
- 03.11.2021
- Beginn
- 04.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Herpes zoster
Varicella virus test positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Herpes zoster
- Hospital-Tage
- -
- Labordaten
- VARICELLA ZOSTER VIRUS DNA, PCR POSITIVE Collected: 11/09/2021 5:00 PM
- Aktuelle Erkrankungen
- nothing worth remembering
- Vorgeschichte
- blood pressure, obesity
- Andere Medikamente
- daily: atenolol 50mg, aspirin 81mg, calcium 1000mg, vitamin d 2000 IU
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 78,0
- Geschlecht
- M
- Eingang
- 23.02.2022
- Impfdatum
- 17.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 3,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Antiplatelet therapy
Embolic cerebral infarction
Symptomtext
COVID-19 booster vaccination on 11/17/2021. Admitted to hospital 11/20/2021 with multiple embolic infarcts. Treated with anti-platelet therapy.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Antiplatelet therapy
- Hospital-Tage
- 2,0
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- DULoxetine (CYMBALTA) Metoprolol Tartrate (LOPRESSOR) 25 mg Aspirin 325 mg Gabapentin (NEURONTIN) 100 mg Tamsulosin (FLOMAX) 0.4 mg Atorvastatin (LIPITOR) 80 mg
- Allergien
- Lisinopril
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 23.02.2022
- Impfdatum
- 22.11.2021
- Beginn
- 20.12.2021
- Tage bis Beginn
- 28,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Burning sensation
Discomfort
Hepatic enzyme increased
Insomnia
Liver function test increased
Magnetic resonance imaging
Metabolic function test
Symptomtext
On 12/20/2021 I thought that I may have had acid reflux because I had a light burning pain in the diaphragm area that lasted for about 2 days. I noticed the sensation again on 1/15/2022, and I made an appointment to see my Doctor on 1/18/2022 because I was unable to sleep that night due to the burning sensation, and pressure feeling in the same area. My doctor ordered blood work that showed I had elevated Liver enzymes. I am still being treated for this condition.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Burning sensation
- Hospital-Tage
- -
- Labordaten
- CMP- Liver function elevated CT scan- waiting to see specialist for results Liver MRI- waiting to see specialist for results
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- shell fish shrimp
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 21.02.2022
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Interchange of vaccine products
Medication error
Symptomtext
RN wrongly administered a Moderna vaccine to a patient scheduled to receive a high-dose flu vaccine. After discovering this medication error just occurred, staff quickly approached the patient and her relative regarding the situation. Previous two doses were Pfizer (this acted like an unintentional 3rd COVID-19 dose). No harm done to patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 63,0
- Geschlecht
- F
- Eingang
- 17.02.2022
- Impfdatum
- 08.11.2021
- Beginn
- 09.02.2022
- Tage bis Beginn
- 93,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: ja
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
Vaccine breakthrough infection
Symptomtext
BREAKTHROUGH COVID INFECTION
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 8,0
- Geschlecht
- M
- Eingang
- 12.02.2022
- Impfdatum
- 10.12.2021
- Beginn
- 10.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
MODERNA ADULT DOSE WAS GIVEN TO PATIENT UNDER 18 YEARS OLD
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- NONE
- Andere Medikamente
- NONE
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 76,0
- Geschlecht
- M
- Eingang
- 02.02.2022
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Received full dose of Moderna booster I/O half dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- PROSTATE CANCER HYPERLIPIDEMIA CKD STAGE 3 (GFR 30-59). BLINDNESS ONE EYE HX OF ATRIAL FIBRILLATION HX OF CHF LUMBAR DISC DEGENERATION
- Andere Medikamente
- PEPOGEST OMEGA 3-DHA-EPA-FISH OIL MULTIVITAMIN WITH MINERALS COENZYME Q10 MAGNESIUM
- Allergien
- Codeine And Opiate Derivatives
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Received full dose of Moderna booster I/O half dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- ASTHMA, UNSPECIFIED HTN (HYPERTENSION) HYPERLIPIDEMIA HYPOTHYROIDISM GERD (GASTROESOPHAGEAL REFLUX DISEASE) BILAT SHOULDER JOINT PAIN POSTMENOPAUSAL HORMONE REPLACEMENT THERAPY HX OF TOTAL HYSTERECTOMY
- Andere Medikamente
- predniSONE CELEBREX Lisinopril Simvastatin NORVASC Estradiol Omeprazole Sertraline Levothyroxine Diltiazem BUSPAR Gabapentin Levothyroxine CALCIUM CARBONATE-VITAMIN D3
- Allergien
- Chlorothiazide, Sulfa
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 54,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Received full dose of Moderna booster I/O half dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE, IN PARTIAL REMISSION HYPERLIPIDEMIA REFLUX ESOPHAGITIS POSTABLATIVE HYPOTHYROIDISM GRAVES DISEASE TRANSIENT CEREBRAL ISCHEMIA MITRAL VALVE REGURGITATION DYSPHAGIA MENOPAUSE HX OF COLONIC POLYP HX OF TOTAL HYSTERECTOMY PELVIC ENDOMETRIOSIS STAGE 3/4
- Andere Medikamente
- LOPRESSOR PROZAC Liothyronine SYNTHROID Pantoprazole Multivitamin-Minerals Cholecalciferol, Vitamin D3, Aspirin
- Allergien
- Adhesive Tape Gabapentin Gluten No Latex Allergy Shellfish Derived Products
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Received full dose of Moderna booster I/O half dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- 1. Cellulitis of great toe of right foot 2. Avulsion of toenail, initial encounter 3. Acute nonintractable headache, unspecified headache type 4. Elevated blood pressure reading
- Vorgeschichte
- DM 1, POLYNEUROPATHY, ANXIETY LOWER ABDOMINAL PAIN FATTY LIVER MAJOR DEPRESSIVE DISORDER, RECURRENT EPISODE W ASSOCIATED FEATURES PRURITUS VULVAE ABNL MAMMOGRAPHY
- Andere Medikamente
- Humalog, insulin pump, Neurontin, Celexa
- Allergien
- Phenergan, Pregabalin
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 02.02.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
Symptomtext
Received full dose of Moderna booster I/O half dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hypothyroidism, Migraine, HTN, Hyperlipidemia, DM1 w/hypoglycemia unawareness, Insulin pump, Autosomal dominant adult polycystic kidney disease, Occipital neuralgia, Schwannoma leg, Fibromyalgia, Vitamin D Deficiency, Bilateral sensorineural hearing loss
- Andere Medikamente
- Neurontin, Hyzaar, Humalog, Humulin NPG, Levothyroxine, Amerge, Zofran,
- Allergien
- lisinopril, Penicillins Class
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 47,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
Received full dose of Moderna booster- I/O half dose, no adverse RX of patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Rheumatoid arthritis, abnormal pap, tobacco user
- Andere Medikamente
- Pepcid, Methotrexate, Folic Acid
- Allergien
- Codeine
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 55,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
Received full dose of Moderna booster I/O half dose, no adv rx for pt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- Microzide, Mobix, Xanax, Protonix, Zocor, Desyrel, Astelin, Norvasc. Lamictal, Inderal, Patanol
- Allergien
- Bee Venom, Pcn
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 28.01.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
Received full dose of Moderna booster I/O half dose, no adv rx to pt
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Atopic dermatitis, Hashimoto thyroiditis, hyperlipidemia, ADHA, bilat tinnitus
- Andere Medikamente
- Desyrel, Levoxyl
- Allergien
- Atorvastatin, Synthroid
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 60,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
Received full dose of Moderna booster I/O half dose, no adv rx
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Rheumatoid arthritis, GERD, Long term immunosuppression therapy, Prediabetes, Leukocytosis, Chromic back pain, osteopenia, erectile dysfunction
- Andere Medikamente
- Synthroid, Celebrex, Roxicodone, Baclofen, Enbrel, Fosamax, Deltasone, Prilosec, Astelin, claritan
- Allergien
- Methotrexate
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 69,0
- Geschlecht
- M
- Eingang
- 28.01.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
Received full dose of Moderna booster I/O half dose, no adverse rx
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- Bronchitis
- Vorgeschichte
- A-fib, Oxygen use, Humoral Immunoglobulin, Diastolic heart failure, Pulm Htn, atherosclerosis of Aorta, CKD
- Andere Medikamente
- Protonix, Viagra, Astelin
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 27.01.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Incorrect dose administered
No adverse event
Symptomtext
No adverse rx, but pt received full Moderna dose and not half dose for booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- Asthma, HTN, Anxiety, DM2, Migraine, Depression, long term opioid therapy, chronic diarrhea, chronic pain syndrome, Fibromyalgia, interstitial cystitis
- Andere Medikamente
- Keflex, zanaflex, oxycodone, cymbalta, prozac, amaryl, lopressor,
- Allergien
- Percocet, Macrodantin, Morphine, PCN, Sulfa, Hydrocodone, Nortriptyline
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 84,0
- Geschlecht
- F
- Eingang
- 25.01.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Member received 0.25 ml Moderna vaccine IM: according to CDC guidelines should have received 0.5 ml Moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Frailty, Osteoporosis, HTN, Rheumatoid Arthritis, Raynauds Syndrome, Osteoarthritis
- Andere Medikamente
- Nizoral, Plaquenil, Procardia XL, Tylenol, Zestril, Arthritis Pain Relief, Lisinopril, Catapres, Calcium Carbonate, Senna Lax, Magnesium Oxide, Preservision, Cholecalciferol, Vitamin D 3
- Allergien
- Sulfa
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 68,0
- Geschlecht
- M
- Eingang
- 24.01.2022
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Underdose
Symptomtext
Member received 0.25 ml Moderna vaccine IM: according to CDC guidelines should have received 0.5 ml Moderna vaccine
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- DM2, Adult OSA Moderate, Hyperlipidemia, HTN, Osteoarthritis
- Andere Medikamente
- Metformin, Tacrolimus, Lisinopril-HCTZ, Toprol XL, Lipitor, Fish oil
- Allergien
- NKDA, NKFA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 19.01.2022
- Impfdatum
- 30.12.2020
- Beginn
- 08.01.2022
- Tage bis Beginn
- 374,0
- Dosis
- UNK
- Route/Site
- IM / OT
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
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
- -
- Alter
- 43,0
- Geschlecht
- M
- Eingang
- 19.01.2022
- Impfdatum
- 21.01.2021
- Beginn
- 08.01.2022
- Tage bis Beginn
- 352,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- ID
- Alter
- 57,0
- Geschlecht
- F
- Eingang
- 18.01.2022
- Impfdatum
- 10.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Tenderness
Tinnitus
Symptomtext
The day after I received my Moderna booster shot on 11/10/2021, I began to hear ringing or buzzing in my left ear on the same side I had my shot. I also had a swollen lymph node on my collarbone and it was tender. That improved, but I have had the ringing/buzzing in my left ear ever since the booster shot. I went to an ENT specialist. She looked in my ear and did not see anything wrong. She recommended a hearing test and or possible MRI. I am interested to understand if this will go away, or if I need a hearing test and MRI. Can I be reimbursed for this cost and the cost to visit the ENT doctor? I have not had this issue before.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- Televisit with family doctor on 12/8/2021 and visited an ENT specialist in December.
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Type II diabetes, controlled A1C is 6.3
- Andere Medikamente
- Vitamin E; Rosuvastatin 10mg 1 daily; Glipizide 10mg 1 daily; Candesartan 16mg 1 daily; 18 units of Levemir insulin injection daily and .50 Ozempic injection (once per week)
- Allergien
- None known
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 53,0
- Geschlecht
- F
- Eingang
- 16.01.2022
- Impfdatum
- 12.11.2021
- Beginn
- 07.01.2022
- Tage bis Beginn
- 56,0
- Dosis
- 3
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested Positive for Covid
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 11.01.2022
- Impfdatum
- 17.11.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 34,0
- Dosis
- UNK
- Route/Site
- - / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Covid positive contact unknown
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Interchange of vaccine products
Symptomtext
Pt was vaccinated outside (country) with COVISHIELD (4/23/21 - lot #4121Z054; 3/10/21 lot #4120Z011). Pt was accidentally given Moderna booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 37,0
- Geschlecht
- F
- Eingang
- 23.12.2021
- Impfdatum
- 21.12.2021
- Beginn
- 21.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Sensation of foreign body
Throat irritation
Symptomtext
25mins post vaccination, pt reports that she has a lump in her throat but she was able to swallow. Called at 12:12 pm for patient complaining of scratchy throat and unable to clear throat after receiving Moderna Booster vaccine. Patient's V/S: BP-109/69, HR-86, RR-18, O2 sat on RA-100%. Continued to observe patient. Patient states, she can swallow without problems, encouraged patient to drink water. Per patient, she is allergic to peanuts and shellfish, NKDA. At 12:18 pm, Benadryl 50 mg PO administered by RN. Patient was able to swallow Benadryl 50 mg capsule without any problem. Continued to monitor patient. 12:19; V/S: BP-117/68, HR-89, RR- 19, O2 sat on RA -99%, patient is talking in full sentences, denies any sob or itching, no rashes, per patient, her mom is waiting in the car, her mom is driving, encouraged patient to drink more water and ambulate around the hallway. Patient will ambulate with RN and will go home when stable. Patient was able to drink more water without any problem. 12:27 V/S: BP-118/71, HR- 83, RR- 18, O2 sat- 99%RA. At 12:50, patient is stable and discharged home. Pt had a scratchy throat w/ prior Moderna vaccinations. Was not reported at the time of booster vaccination.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Sensation of foreign body
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: Carpal Tunnel syndrome, Depression, substance use in remission, suicide attempt, hx of Child abuse
- Andere Medikamente
- Medications: ferrous sulfate 325 mg (65 mg iron) tablet Take 1 tablet by mouth daily. norethindrone (ORTHO MICRONOR) 0.35 mg tablet Take 1 tablet by mouth daily. sertraline (ZOLOFT) 100 MG tablet Take 1.5 tablets (150 mg total) by mouth dai
- Allergien
- Allergies: peanuts (hives), shellfish (anaphylaxis), Moderna Vaccine (itchy throat)
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 23,0
- Geschlecht
- F
- Eingang
- 20.12.2021
- Impfdatum
- 14.12.2021
- Beginn
- 14.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Feeling hot
Flushing
Symptomtext
20mins post vaccination, pt reported feeling hot/flushed in the face. Vitals: 11:36 108/71, 97, 18-20, 100% -- > 106/69, 92, 18-20, 100% Pt stable and released from the vaccination site @11:46. Pt states she feels better. Pt wishes to go home.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling hot
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: IBS-Mixed, Anxiety, Migraines, HX of Covid-19 infection Dec 2020 w/ lost of taste/smell.
- Andere Medikamente
- Medications: levonorgestrel-ethinyl Estrada 0.15-0.03 mg per tablet- Take 1 Tablet by mouth daily; cetirizine (ZYRTEC) 10 mg tablet; Indications: Urticaria- Take 1 Tablet by mouth once daily; hydrocortisone 2.5 % cream; Indications: Urticar
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 17,0
- Geschlecht
- F
- Eingang
- 17.12.2021
- Impfdatum
- 24.11.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
pt given this vaccine at age 17 when authorized only age 18+ no reported ADE
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- mental health only
- Andere Medikamente
- lamotrigine & sertraline
- Allergien
- pcn allergy
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 81,0
- Geschlecht
- M
- Eingang
- 16.12.2021
- Impfdatum
- 15.12.2021
- Beginn
- 15.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
No adverse event
Underdose
Symptomtext
Pt was due for his second dose of Moderna COVID vaccine primary series which should have been a 0.5 mL dose. However the medical assistant who administered this dose unintentionally administered 0.25 mL instead (lower than authorized dose). This incident occurred on 12/15/21. The medical assistant involved notified me of this incident today, 12/16/21. No adverse effect has occurred.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- none needed
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- Chronic: Afib, aortic stenosis, CAD with STEMI s/p 4v CABG, CKD, hypertension
- Andere Medikamente
- Eliquis 2.5 mg twice daily, aspirin 81 mg once daily, atorvastatin 80 mg once daily, fish oil 1000 mg once daily, furosemide 40 mg: 1.5 tabs twice daily, lisinopril 5 mg twice daily, metoprolol tartrate 25 mg twice daily, Centrum Silver onc
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- MA
- Alter
- 14,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 12.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Exposure during pregnancy
Prenatal care
Staphylococcal infection
Staphylococcus test positive
Symptomtext
Patient is a 14 year old and 18 weeks 1 day of gestation at the time of event was erroneously counseled and given the Moderna Covid vaccine on 11/12/21 at 9:58 am on left arm. This was done during her initial prenatal intake where she presented as a new arrival, late to care and counseled by Certified Nurse Midwife who also administered the vaccine.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Exposure during pregnancy
- Hospital-Tage
- -
- Labordaten
- None at the time.
- Aktuelle Erkrankungen
- UTI (urinary tract infection) during pregnancy (Greater than 100,000 CFU/mL of Staphylococcus saprophyticus); diagnosed 11/24/21; treated
- Vorgeschichte
- None to report
- Andere Medikamente
- Pyridoxine HCl (VITAMIN B-6) 25 MG Tablet; 1 tablet by mouth, 3 times daily as needed (nausea/vomiting) Doxylamine Succinate, Sleep, (UNISOM SLEEPTABS) 25 MG Tablet; 1 tablet by mouth at night if needed (nausea/vomiting) ondansetron hcl (ZO
- Allergien
- No known allergies
- Vorherige Impfungen
- -
- Staat
- IL
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 15.12.2021
- Impfdatum
- 07.11.2021
- Beginn
- 07.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Underdose
Symptomtext
Error: Wrong Dose of Vaccine - Too Low-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Underdose
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 13,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 04.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / AR
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Product administered to patient of inappropriate age
Symptomtext
Underage person received vaccine - no adverse event
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 62,0
- Geschlecht
- F
- Eingang
- 14.12.2021
- Impfdatum
- 04.12.2021
- Beginn
- 04.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
No adverse event
Symptomtext
Pt received full dose Moderna instead of Moderna Booster dose. No adverse effects noted at the time of vaccination or after observation. Pt stable and released from the vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- Unknown
- Andere Medikamente
- Unknown
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 34,0
- Geschlecht
- F
- Eingang
- 13.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Feeling hot
Symptomtext
20mins post vaccination, pt reported feeling hot while sitting in observation and clamminess on forhead noted. No dizziness reported. Taken to back med room. NO other adverse symptoms reported. Vitals: 14:17 107/69, 52, 20, 97.9F, 100% O2 Sat -- > 14:27 106/69, 63, 20, 100% Pt given orange juice and water. pt ambulated on her own. no dizziness reported. Pt reported feeling better after dinking fluids. Pt educated to eat and drink beofre needlesticks in future as pt reported that she did not have lunch before coming. Pt reported feeling back to normal before leaving facility @14:30. Pt had steady gait and no s/s of distress. Pt stable and released from the vaccination site.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling hot
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: Infertility
- Andere Medikamente
- Medication: Prenatal vitamin
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Vaccine administered at 20 days instead of 28 days between doses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 44,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Vaccine administered at 20 days instead of 28 days between doses.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Vaccine administered at 20 days instead of 28 days from 1st dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 21,0
- Geschlecht
- F
- Eingang
- 08.12.2021
- Impfdatum
- 08.12.2021
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Symptomtext
Vaccine administered at 20 days instead of 28 days from 1st dose.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- NA
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 07.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Heart rate increased
Symptomtext
Patient has been experienced increased heart rate up to 135 for the last 4-5 days after getting her booster dose. Patient called pharmacy on 12/6/2021 at around 3pm stating that she has been experienced increased heart rate up to 135 for the last 4-5 days after getting her booster dose. Patient had history of heart surgery. Pharmacist recommended patient to see her cardiologist as soon as possible.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Heart rate increased
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- NONE
- Vorgeschichte
- HEART DISEASE
- Andere Medikamente
- -
- Allergien
- NKA
- Vorherige Impfungen
- -
- Staat
- GA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 03.12.2021
- Impfdatum
- 01.12.2021
- Beginn
- 03.12.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Lymphadenopathy
Symptomtext
Client presented to HD on 12/3/2021. She complains of swollen lymph node to axilla region right arm. Injection site is free of swelling or redness.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Lymphadenopathy
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- unknown
- Allergien
- nkda
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 02.12.2021
- Impfdatum
- 02.12.2021
- Beginn
- 02.12.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Product storage error
Symptomtext
Our patient received a Moderna booster dose that was in room temperature less than 24 hours, but longer than the recommended time from initial puncture. He was informed of the incident and stated that he feels well, with no rash, fever, SOB, or any unusual symptoms. Reported incident to Moderna , and waiting response on the validity of the booster dose given.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product storage error
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 30.11.2021
- Impfdatum
- 21.01.2021
- Beginn
- 27.11.2021
- Tage bis Beginn
- 310,0
- Dosis
- UNK
- Route/Site
- IM / UN
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
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
- -
- Alter
- 58,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 20.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Pharyngeal swelling
Symptomtext
Pt received Pfizer Primary Series w/ Moderna Booster 20mins post vaccination pt c/o throat swelling. No tongue or lip swelling noted or reported Vitals: 143/85, 70, 20, 99% Pt declined benadryl stating " I have allergy meds at home". Vitals remained stable, O2 above 98% throughout observation. pt talking and breathing normally. Pt released to husband and daughter in stable condition w/ instructions to f/u w/ PCP and ER precautions.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Pharyngeal swelling
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: Fibromyalgia 11/14/2021 Primary generalized (osteo)arthritis 11/14/2021 Cervical spondylosis 11/14/2021 Shoulder impingement syndrome, right 11/14/2021 Elevated antibody levels 11/14/2021
- Andere Medikamente
- Medications: Amitriptyline 25mg PO QHS Lisinopril 40mg Daily Metformin 500mg daily meloxicam 15mg PO PRN Daily
- Allergien
- Allergies: Morphine ("pt felt like she was going to die"), Sulfa (hives, urticaria), black sesame seeds
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 43,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 20.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- N/A
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Interchange of vaccine products
Symptomtext
Patient (passenger) was registered for Pfizer booster and was in the same car as her husband (driver) who was registered for Moderna. They were sent to the Moderna lane and were correctly checked in for their respective boosters. However, the vaccinator administered the Moderna booster for both patients instead of the Pfizer booster for the passenger. Nurse informed her lead and pharmacist of the error. Patient was informed of the error by the pharmacist and addressed all her questions & concerns.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- N/A
- Vorgeschichte
- N/A
- Andere Medikamente
- N/A
- Allergien
- N/A
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Booster given prior to recommended due date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 62,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Booster given prior to recommended due date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 38,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Booster given prior to recommended due date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 35,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Booster given prior to recommended due date.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Booster given prior to recommended due date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 31,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Booster given prior to recommended due date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 20,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Booster given prior to recommended due date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Incorrect dose administered
Symptomtext
Booster given prior to recommended due date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 37,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Booster given prior to recommended due date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 30,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
Booster given prior to recommended due date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 40,0
- Geschlecht
- M
- Eingang
- 29.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Extra dose administered
Inappropriate schedule of product administration
Symptomtext
Booster given prior to recommended due date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NJ
- Alter
- 26,0
- Geschlecht
- F
- Eingang
- 29.11.2021
- Impfdatum
- 23.11.2021
- Beginn
- 23.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Symptomtext
Booster given prior to due date
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- -
- Alter
- 70,0
- Geschlecht
- F
- Eingang
- 24.11.2021
- Impfdatum
- 19.11.2021
- Beginn
- 19.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: ja
Erholt: unbekannt
Swollen tongue
Symptomtext
Pt finished her 20 minute observation time and left. She was sitting in her car watching videos when she noticed her tongue started to swell. We brought her back in via wheelchair to Medical Bay for further assessment. Vitals stable A&Ox4 no rep distress, no difficulty swallowing. 75mins post vaccination pt reported tongue swelling. Pt reported that she had no previous reaction to 1st or 2nd Dose Moderna Vitals: 127/70, 86, 18, 97% on RA Pt given Benadryl 50mg PO @10:50 and 0.3mg IM Epi @11:20 to Right lateral thigh. Patient observed longer and no change in size of tongue swelling. EMS was called at 12:10 due to persistent symptoms and need for additional observation. Pt taken to the ER @12:23. NO additional information available to this writer
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Swollen tongue
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- PMH: PRIMARY GENERALIZED (OSTEO)ARTHRITIS OTHER CHRONIC PAIN FIBROMYALGIA RHEUMATOID ARTHRITIS, UNSPECIFIED OTHER SPECIFIED ANXIETY DISORDERS POLYCYSTIC KIDNEY, ADULT TYPE HYPERTENSIVE CHRONIC KIDNEY DISEASE W STG 1-4/UNSP CHR KDNY CHRONIC KIDNEY DISEASE, STAGE 3 UNSPECIFIED GOUT DUE TO RENAL IMPAIRMENT, UNSPECIFIED SITE MILD PERSISTENT ASTHMA, UNCOMPLICATED SJOGREN SYNDROME, UNSPECIFIED OBSTRUCTIVE SLEEP APNEA (ADULT) (PEDIATRIC) MORBID (SEVERE) OBESITY DUE TO EXCESS CALORIES HISTORY OF FALLING PROBLEMS RELATED TO LIVING ALONE LONG TERM (CURRENT) USE OF ANTICOAGULANTS PRESENCE OF ARTIFICIAL KNEE JOINT, BILATERAL PRESENCE OF ARTIFICIAL HIP JOINT, BILATERAL BODY MASS INDEX [BMI] 36.0-36.9, ADULT PERSONAL HISTORY OF PULMONARY EMBOLISM PERSONAL HISTORY OF OTHER VENOUS THROMBOSIS AND EMBOLISM
- Andere Medikamente
- Medications: clotrimazole-betamethasone 1 %-0.05 % topical cream Per instructions ONE TIME PER DAY (route: topical) desonide 0.05 % topical ointment Per instructions ONE TIME PER DAY (route: topical) albuterol sulfate HFA 90 mcg/actuati
- Allergien
- Allergies: Codeine (vomiting), Lactose, lactase
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 24.11.2021
- Impfdatum
- 24.11.2021
- Beginn
- 24.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Patient presented to the vaccination site on 11/13/21. The client notified RN that he received a complete series of COVID vaccine first dose on 12/22/2O and second dose on 1/20/21. RN submitted a medical consult via text message to Vaccine Operations Leads, requesting to proceed with the COVID vaccine Moderna booster. Per CDC guidance, approval to proceed with COVID vaccine Moderna was obtained from medical consult team via text message from , Vaccine Operations Lead . Client received COVID vaccine Moderna Lot#066F21A on 11/13/21. The client did not report any symptoms during the 15 minute observation period. Vaccinator educated client on possible adverse reactions and when to seek medical care. Client reported no symptoms.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- NONE
- Aktuelle Erkrankungen
- unknown
- Vorgeschichte
- unknown
- Andere Medikamente
- unknown
- Allergien
- unknown
- Vorherige Impfungen
- -
- Staat
- KY
- Alter
- 60,0
- Geschlecht
- F
- Eingang
- 23.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 8,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
COVID-19
SARS-CoV-2 test positive
Symptomtext
Tested Positive for Covid
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- COVID-19
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 49,0
- Geschlecht
- F
- Eingang
- 23.11.2021
- Impfdatum
- 12.11.2021
- Beginn
- 01.11.2021
- Tage bis Beginn
- -
- Dosis
- 3
- Route/Site
- OT / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Lymphadenopathy
Symptomtext
Inappropriate schedule of vaccine administered; Lymph nodes swelling/ Lymph node of the size of a grape fruit; This spontaneous case was reported by a consumer and describes the occurrence of LYMPHADENOPATHY (Lymph nodes swelling/ Lymph node of the size of a grape fruit) and INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) in a 49-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. Previously administered products included for Product used for unknown indication: PFIZER BIONTECH COVID-19 VACCINE (The patient received the 1st and 2nd dose of Pfizer). Past adverse reactions to the above products included No adverse event with PFIZER BIONTECH COVID-19 VACCINE. Concomitant products included DULOXETINE HYDROCHLORIDE (CYMBALTA) for an unknown indication. On 12-Nov-2021, the patient received third dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 12-Nov-2021, the patient experienced INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered). In November 2021, the patient experienced LYMPHADENOPATHY (Lymph nodes swelling/ Lymph node of the size of a grape fruit). The patient was treated with IBUPROFEN (ADVIL [IBUPROFEN]) for Adverse event, at an unspecified dose and frequency. On 12-Nov-2021, INAPPROPRIATE SCHEDULE OF PRODUCT ADMINISTRATION (Inappropriate schedule of vaccine administered) had resolved. At the time of the report, LYMPHADENOPATHY (Lymph nodes swelling/ Lymph node of the size of a grape fruit) outcome was unknown. Other concomitant medications included Birth control pill. The patient received the 1st and 2nd dose of Pfizer and the booster shot of Moderna. The patient got lymph nodes swelling and lymph node of the size of a grape fruit. To treat the symptoms, the patient took Advil last night and this morning.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- CYMBALTA
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- F
- Eingang
- 22.11.2021
- Impfdatum
- 18.11.2021
- Beginn
- 18.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Dysgeusia
Parosmia
Throat irritation
Symptomtext
Client received 2nd Moderna COVID vaccine at 1:12 pm in left deltoid, while sitting in zero gravity chair. At 1:15 pm, client reports to EMT she has an itchy feeling in throat, with a metallic taste in her mouth. Client also reports she perceives a "sense of perfume smell in air" as another client passed by. Client reports she is allergic to perfume. Client denies shortness of breath, no trouble breathing, no trouble swallowing, or chest tightening. RN offers client Benadryl IM, client declines, states Benadryl is not for itchy throat and is concerned it will interfere with the efficacy of COVID vaccine. Client states she would like to wait and see if symptoms resolve as she believes they are related to the perfume she smelled in the air. Vital signs are stable. EMT continues to maintain conversation with client, client reports sensation of "perfume smell" has gone away. At 1:35 pm, client reports throat itchiness is improving, declines Benadryl once again. At 1:38 pm, client reports no more throat itchiness. At 1:40 pm, Client reports throat sensation and itchiness have completely resolved, reports slight headache because of perfume noted earlier. Client educated on ER precautions. Client left observation area at 1:50 pm, walking with steady gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Dysgeusia
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- bee stings, spiders, fleas, eggs, fructose, potatoes, nuts, peppers, morphine, opiates, anti-nausea medications
- Vorherige Impfungen
- -
- Staat
- WA
- Alter
- 36,0
- Geschlecht
- M
- Eingang
- 21.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 20.11.2021
- Tage bis Beginn
- 19,0
- Dosis
- 1
- Route/Site
- SYR / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Deafness unilateral
Diplacusis
SARS-CoV-2 test negative
Symptomtext
Went home felt fine, took a nap, woke up with significant hearing loss in one ear, about 18 hours after injection loss is near total, loud metallic sounding echo when people talk.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Deafness unilateral
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- Persistent cough lasting 3 or 4 months, tested for covid, negative for that and pneumonia.
- Vorgeschichte
- Hypertension
- Andere Medikamente
- lisinopril - 25mg daily
- Allergien
- None
- Vorherige Impfungen
- The first round of Moderna vaccines caused anosmia (loss of taste) after the second dose.
- Staat
- MI
- Alter
- 8,0
- Geschlecht
- F
- Eingang
- 19.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Product administered to patient of inappropriate age
Symptomtext
This spontaneous case was reported by a pharmacist and describes the occurrence of PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (9 year old received full dose of Moderna) in a 9-year-old female patient who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no. 066F21A) for COVID-19 vaccination. No Medical History information was reported. On 11-Nov-2021, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form. On 11-Nov-2021, the patient experienced PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (9 year old received full dose of Moderna). On 11-Nov-2021, PRODUCT ADMINISTERED TO PATIENT OF INAPPROPRIATE AGE (9 year old received full dose of Moderna) had resolved. For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter did not provide any causality assessments. No Concomitant medication information was reported. No Treatment medications were provided
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Product administered to patient of inappropriate age
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- PA
- Alter
- 67,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 15.11.2021
- Beginn
- 15.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Infection
Symptomtext
Error: Infection / Cellulitis (diagnosed by MD)-
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cellulitis
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- MN
- Alter
- 64,0
- Geschlecht
- F
- Eingang
- 18.11.2021
- Impfdatum
- 01.11.2021
- Beginn
- 02.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect route of product administration
Symptomtext
RN administered the Moderna COVID booster in the low on the arm, not in the deltoid.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect route of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 42,0
- Geschlecht
- M
- Eingang
- 17.11.2021
- Impfdatum
- 16.11.2021
- Beginn
- 17.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Electrocardiogram
No adverse event
Symptomtext
Client reported to vaccinator RN that he experienced chest pain and SOB after his 2nd dose Moderna COVID vaccine on 04/11/2021 that resulted in hospitalization for approximately 48 hours. Client reported onset of adverse reactions was about 24 hours after receiving his 2nd dose Moderna COVID vaccine. Client reported he recieved pain medication for treatment in the hospital and was advised by PCP to proceed with receiving Moderna Booster. Lead RN submitted a medical consult via test message to Vaccine Operations Leads, requesting to proceed with the COVID vaccine Moderna Booster. RN received approval from MD to proceed with Moderna Booster. Client received COVID vaccine Moderna Booster (lot# 066F21A) at approximately 0315 in the R deltoid and was instructed to be observed 30 minutes and f/u with PCP. No adverse reactions reported during observation. Client left vaccine site with steady and symmetrical gait.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Electrocardiogram
- Hospital-Tage
- -
- Labordaten
- EKG
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- Anaphylactic allergy to Penicillin
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 14.11.2021
- Impfdatum
- 09.11.2021
- Beginn
- 09.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
No adverse event
Symptomtext
The patient was presented to the vaccination site on 11/09/21. The client notified RN that after her first dose of the COVID Moderna vaccine on 1/16/21 client reported feeling dizzy after an hour from getting vaccine. Client stated that the dizziness lasted about an hour. Client also stated that after her second dose of the COVID Moderna vaccine on 2/13/21 she also experienced the same symptom of dizziness but this time it was only for 30 minutes. RN submitted a medical consult via text message to Vaccine Operations Leads, requesting to proceed with the COVID vaccine Moderna booster dose. Approval to proceed with COVID vaccine Moderna booster dose was obtained from medical consult team, Vaccine Operations Lead , RN via text message. Client received COVID vaccine Moderna booster dose Lot# 066F21A on 11/09/2021. The client did not report any symptoms during the 30 minute observation period. The client left the vaccination site at 1505 unassisted with a steady gait. Clients boyfriend stated that he would drive her home. RN educated client on worsening signs and symptoms of receiving booster Moderna COVID vaccine and when to seek EMS, urgent care, or go to the ED. Client verbalized understanding.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- F
- Eingang
- 13.11.2021
- Impfdatum
- 13.11.2021
- Beginn
- 13.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Inappropriate schedule of product administration
Interchange of vaccine products
Symptomtext
Client presented to the vaccintaion site on 11/13/21. The client notified RN that she received a single dose of Pfizer COVID vaccine on 03/05/21. Submitted medical consult via text to Vaccine Operations Leads, requesting to proceed with the COVID vaccine of Moderna. Per CDC guidance, approval to proceed with COVID vaccine Moderna Lot#066F21A was obtained from MD via text message from, Vaccine Operations Lead. The client did not report any symptoms during the 30 minute observation period. RN educated client on possible adverse reactions and when to seek medical care. The client left the vaccination site at 1430 hours and stated that they were "good" and appeared to be wnl at time of departure.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- hypertension
- Andere Medikamente
- Cozaar, scopalomine, hormone replacement therapy.
- Allergien
- Mango, erythromycin, demerol, flagyl.
- Vorherige Impfungen
- Client had a reaction to first dose Pfizer on 03/05/2021. S/S n/v for 10 days and vertigo beginning on day 3. MD prescribed sc
- Staat
- CA
- Alter
- 55,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 1,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Interchange of vaccine products
Symptomtext
Client presented to the vaccination site on 11/11/2021. The client notified RN that he she received a single dose of Sputnik COVID vaccine on 06/05/21 and Moderna First dose 08/28/2021. RN submitted a medical consult via phone number to Vaccine Operations Leads, requesting to proceed with the COVID vaccine Moderna second dose. Per CDC guidance, approval to proceed with COVID vaccine Moderna was obtained from medical consult team via phone by Vaccine Operations Lead. Client received COVID vaccine Moderna Lot#066F21A on 11/11/21. The client did not report any symptoms during the 15 minute observation period. RN educated client on possible adverse reactions and when to seek medical care. The client left the vaccination site in a steady gait
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- None
- Andere Medikamente
- None
- Allergien
- None
- Vorherige Impfungen
- -
- Staat
- OH
- Alter
- 38,0
- Geschlecht
- F
- Eingang
- 12.11.2021
- Impfdatum
- 10.11.2021
- Beginn
- 12.11.2021
- Tage bis Beginn
- 2,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Cellulitis
Symptomtext
Per pt, she saw an urgent care doctor and she is on antibiotics. Per pt she said MD told her she has cellulitis due to Covid injection
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Cellulitis
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- Blood Dyscrasia
- Vorgeschichte
- n/a
- Andere Medikamente
- not available
- Allergien
- NKDA
- Vorherige Impfungen
- -
- Staat
- MI
- Alter
- 8,0
- Geschlecht
- F
- Eingang
- 11.11.2021
- Impfdatum
- 11.11.2021
- Beginn
- 11.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Interchange of vaccine products
Symptomtext
Nothing at the moment (5 hours have passed). Patient came in for the Pfizer kids shot but received a dose of a booster shot of Moderna.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CO
- Alter
- 46,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 06.11.2021
- Beginn
- 06.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Incorrect dose administered
Symptomtext
Received full dose of Moderna booster instead of half dose
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- None
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hyperlipidemia, Sever Obesity, OSA, Alopecia, Gout
- Andere Medikamente
- Adderall, Trazadone, Crestor, Allopurinol
- Allergien
- Beta Adrenergic blockers, Celecoxib, Promethazine Hydrochloride, Sulfa drugs
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 52,0
- Geschlecht
- M
- Eingang
- 11.11.2021
- Impfdatum
- 08.11.2021
- Beginn
- 08.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / -
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Extra dose administered
Symptomtext
Pt presented to the vaccination site on 11/08/21. The client notified RN after 1-2 hours after receiving his second dose he felt like his heart was racing. The client went to the emergency room and they kept him in observation for 4-5 hours. They did not give him any medications. Client stated that he was then sent home. Client stated that the next day he felt the same symptom of his heart racing and returned to the hospital. Client stayed at the hospital in observation from 1100-2100 that day. Client stated that he felt his hear racing on and off the entire time. Client was sent home after staying in observation for 10 hours. Client was not given any medications. RN submitted a medical consult via text message to Vaccine Operations Leads, requesting to proceed with the COVID Moderna booster vaccine. Approval to proceed with COVID vaccine Moderna booster with 15 minute observation was obtained from medical consult team, Vaccine Operations Lead, RN via text message. Client received COVID Moderna booster vaccine Lot# 066F21A on 11/08/2021. The client did not report any symptoms during the observation period. RN educated client on worsening signs and symptoms of COVID vaccine and when to seek EMS, urgent care or when to return to ED if symptoms return. Client verbalized understanding. The client left the vaccination site at 1415.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 27,0
- Geschlecht
- F
- Eingang
- 10.11.2021
- Impfdatum
- 10.11.2020
- Beginn
- 10.11.2021
- Tage bis Beginn
- 365,0
- Dosis
- 1
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Feeling abnormal
Symptomtext
Patient complained of throat "feeling funny" about 5 -10 minutes post vaccine admin but did not complain of problems breathing or swallowing. Administered 25mg of diphenhydramine by mouth. Continued to closely monitor. Patient was alert and continued to improve after administration of diphenhydramine over the course of approximately 30 minutes after admin.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Feeling abnormal
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 06.11.2021
- Impfdatum
- 11.03.2021
- Beginn
- 30.07.2021
- Tage bis Beginn
- 141,0
- Dosis
- 3
- Route/Site
- SYR / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Magnetic resonance imaging head
Scan with contrast
Tinnitus
Symptomtext
Tinnitus in ears appeared approximately 3 months after the second injection.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Magnetic resonance imaging head
- Hospital-Tage
- -
- Labordaten
- 10/13/2021: MR BRAIN INTERNAL AUDITORY CANAL TEMPORAL BONE W AND WO IV CONTRAST
- Aktuelle Erkrankungen
- None
- Vorgeschichte
- Hay fever
- Andere Medikamente
- Allopurinol, amlopidine
- Allergien
- Statins
- Vorherige Impfungen
- -
- Staat
- NC
- Alter
- 66,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
No adverse event
Wrong product administered
Symptomtext
patient was expecting to get pfizer booster and instead moderna booster (0.25ml) was administered to the patient. no adverse reaction noted after giving moderna
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- No adverse event
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 49,0
- Geschlecht
- M
- Eingang
- 05.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 2
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: ja
Interchange of vaccine products
No adverse event
Symptomtext
Patient was in clinic today to receive booster shot of Janssen vaccine. Patient received first Janssen vaccine on 5/28/21. Patient requested a Janssen booster shot but was given a Moderna booster shot instead. Moderna booster was given before the 6 month period dictated by Moderna manufacturer and CDC. No adverse events reported by patient. No follow on care needed for patient.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Interchange of vaccine products
- Hospital-Tage
- -
- Labordaten
- none
- Aktuelle Erkrankungen
- none
- Vorgeschichte
- none
- Andere Medikamente
- none
- Allergien
- none
- Vorherige Impfungen
- -
- Staat
- CA
- Alter
- 65,0
- Geschlecht
- F
- Eingang
- 05.11.2021
- Impfdatum
- 05.11.2021
- Beginn
- 05.11.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / RA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Inappropriate schedule of product administration
Product administration error
Symptomtext
Administration error: Booster vaccine at 3 months, instead of recommended 6 month interval. Hx of Heart disease. Pt monitored for 1.5 hours after administration, no side effects noted. VS Stable.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Inappropriate schedule of product administration
- Hospital-Tage
- -
- Labordaten
- N/A
- Aktuelle Erkrankungen
- AV Block s/p pacemaker HTN Overweight
- Vorgeschichte
- As above
- Andere Medikamente
- Isosorbide Dinitrate tab 30mg qD Metoprolol Succinate ER 100mg qD
- Allergien
- Allergic to Lisinopril
- Vorherige Impfungen
- -
- Staat
- WV
- Alter
- 66,0
- Geschlecht
- M
- Eingang
- 31.10.2021
- Impfdatum
- 31.10.2021
- Beginn
- 31.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: unbekannt
Incorrect dose administered
Symptomtext
PATIENT WAS A TRANSPLANT PATIENT AND SHOULD HAVE RECEIVED AN ADDITIONAL DOSE 0.5ML, INSTEAD IN ERROR RECEIVED A BOOSTER 0.25ML.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Incorrect dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -
- Staat
- NY
- Alter
- 51,0
- Geschlecht
- M
- Eingang
- 29.10.2021
- Impfdatum
- 29.10.2021
- Beginn
- 29.10.2021
- Tage bis Beginn
- 0,0
- Dosis
- 3
- Route/Site
- IM / LA
Tod: unbekannt
Lebensbedrohlich: unbekannt
Hospital: unbekannt
Disable: unbekannt
ER: unbekannt
Erholt: nein
Extra dose administered
Symptomtext
Did not qualify for booster
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Extra dose administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -